WorldWideScience

Sample records for calcium silicate cements

  1. Premixed calcium silicate cement for endodontic applications

    OpenAIRE

    Persson, Cecilia; Engqvist, Håkan

    2011-01-01

    Calcium silicate-based materials (also called MTA) are increasingly being used in endodontic applications. However, the handling properties of MTA are not optimal when it comes to injectability and cohesion. Premixing the cements using glycerol avoids these issues. However, there is a lack of data on the effect of common cement variables on important properties of premixed cements for endodontic applications. In this study, the effects of liquid-to-powder ratio, amount of radiopacifier and am...

  2. Nanostructure of Calcium Silicate Hydrates in Cements

    KAUST Repository

    Skinner, L. B.

    2010-05-11

    Calcium silicate hydrate (CSH) is the major volume phase in the matrix of Portland cement concrete. Total x-ray scattering measurements with synchrotron x rays on synthetic CSH(I) shows nanocrystalline ordering with a particle diameter of 3.5(5) nm, similar to a size-broadened 1.1 nm tobermorite crystal structure. The CSH component in hydrated tricalcium silicate is found to be similar to CSH(I). Only a slight bend and additional disorder within the CaO sheets is required to explain its nanocrystalline structure. © 2010 The American Physical Society.

  3. Dentin-cement Interfacial Interaction: Calcium Silicates and Polyalkenoates

    OpenAIRE

    Atmeh, A.R.; Chong, E. Z.; Richard, G; Festy, F.; Watson, T.F.

    2012-01-01

    The interfacial properties of a new calcium-silicate-based coronal restorative material (Biodentine™) and a glass-ionomer cement (GIC) with dentin have been studied by confocal laser scanning microscopy (CLSM), scanning electron microscopy (SEM), micro-Raman spectroscopy, and two-photon auto-fluorescence and second-harmonic-generation (SHG) imaging. Results indicate the formation of tag-like structures alongside an interfacial layer called the “mineral infiltration zone”, where the alkaline c...

  4. Enhanced bioactivity of glass ionomer cement by incorporating calcium silicates.

    Science.gov (United States)

    Chen, Song; Cai, Yixiao; Engqvist, Håkan; Xia, Wei

    2016-01-01

    Glass ionomer cements (GIC) are known as a non-bioactive dental cement. During setting the GIC have an acidic pH, driven by the acrylic acid component. It is a challenge to make GIC alkaline without disturbing its mechanical properties. One strategy was to add slowly reacting systems with an alkaline pH. The aim of the present study is to investigate the possibility of forming a bioactive dental material based on the combination of glass ionomer cement and calcium silicates. Two types of GIC were used as control. Wollastonite (CS also denoted β-CaSiO3) or Mineral Trioxide Aggregate (MTA) was incorporated into the 2 types of GIC. The material formulations' setting time, compressive strength, pH and bioactivity were compared between modified GIC and GIC control. Apatite crystals were found on the surfaces of the modified cements but not on the control GIC. The compressive strength of the cement remained with the addition of 20% calcium silicate or 20% MTA after one day immersion. In addition, the compressive strength of GIC modified with 20% MTA had been increased during the 14 d immersion (p < 0 .05). PMID:26787304

  5. Vibrational investigation of calcium-silicate cements for endodontics in simulated body fluids

    Science.gov (United States)

    Taddei, Paola; Modena, Enrico; Tinti, Anna; Siboni, Francesco; Prati, Carlo; Gandolfi, Maria Giovanna

    2011-05-01

    Calcium-silicate MTA (Mineral Trioxide Aggregate) cements have been recently developed for oral and endodontic surgery. This study was aimed at investigating commercial (White ProRoot MTA, White and Grey MTA-Angelus) and experimental (wTC-Bi) accelerated calcium-silicate cements with regards to composition, hydration products and bioactivity upon incubation for 1-28 days at 37 °C, in Dulbecco's Phosphate Buffered Saline (DPBS). Deposits on the surface of the cements and the composition changes during incubation were investigated by micro-Raman and ATR/FT-IR spectroscopy, and pH measurements. Vibrational techniques disclosed significant differences in composition among the unhydrated cements, which significantly affected the bioactivity as well as pH, and hydration products of the cements. After one day in DPBS, all the cements were covered by a more or less homogeneous layer of B-type carbonated apatite. The experimental cement maintained a high bioactivity, only slightly lower than the other cements and appears a valid alternative to commercial cements, in view of its adequate setting time properties. The bioactivity represents an essential property to favour bone healing and makes the calcium-silicate cements the gold standard materials for root-apical endodontic surgery.

  6. In Vitro Cytotoxicity of Calcium Silicate-Based Endodontic Cement as Root-End Filling Materials

    OpenAIRE

    Selen Küçükkaya; Mehmet Ömer Görduysus; Naciye Dilara Zeybek; Sevda Fatma Müftüoğlu

    2016-01-01

    The aim of this study was to evaluate the cytotoxicity of three types of calcium silicate-based endodontic cement after different incubation periods with human periodontal ligament fibroblasts. Human periodontal ligament fibroblasts were cultured from extracted third molars and seeded in 96-well plates. MTA, calcium enriched mixture (CEM) cement, and Biodentine were prepared and added to culture insert plates which were immediately placed into 96-well plates containing cultured cells. After i...

  7. Characterization of modified calcium-silicate cements exposed to acidic environment

    Energy Technology Data Exchange (ETDEWEB)

    Camilleri, Josette, E-mail: josette.camilleri@um.edu.mt

    2011-01-15

    Portland cement which is used as a binder in concrete in the construction industry has been developed into a biomaterial. It is marketed as mineral trioxide aggregate and is used in dentistry. This material has been reported to be very biocompatible and thus its use has diversified. The extended use of this material has led to developments of newer versions with improved physical properties. The aim of this study was to evaluate the effect of acidic environments found in the oral cavity on fast setting calcium silicate cements with improved physical properties using a combination of techniques. Two fast setting calcium silicate cements (CSA and CFA) and two cement composites (CSAG and CFAG) were assessed by subjecting the materials to lactic acid/sodium lactate buffer gel for a period of 28 days. At weekly intervals the materials were viewed under the tandem scanning confocal microscope (TSM), and scanning electron microscope (SEM). The two prototype cements exhibited changes in their internal chemistry with no changes in surface characteristics. Since the changes observed were mostly sub-surface evaluation of surface characteristics of cement may not be sufficient in the determination of chemical changes occurring. - Research Highlights: {yields} An acidic environment affects modified fast setting calcium silicate-based cements. {yields} No surface changes are observed in acidic environment. {yields} An acidic environment causes sub-surface changes in the material chemistry which are only visible in fractured specimens. {yields} A combination of techniques is necessary in order to evaluate the chemical changes occurring.

  8. Characterization of modified calcium-silicate cements exposed to acidic environment

    International Nuclear Information System (INIS)

    Portland cement which is used as a binder in concrete in the construction industry has been developed into a biomaterial. It is marketed as mineral trioxide aggregate and is used in dentistry. This material has been reported to be very biocompatible and thus its use has diversified. The extended use of this material has led to developments of newer versions with improved physical properties. The aim of this study was to evaluate the effect of acidic environments found in the oral cavity on fast setting calcium silicate cements with improved physical properties using a combination of techniques. Two fast setting calcium silicate cements (CSA and CFA) and two cement composites (CSAG and CFAG) were assessed by subjecting the materials to lactic acid/sodium lactate buffer gel for a period of 28 days. At weekly intervals the materials were viewed under the tandem scanning confocal microscope (TSM), and scanning electron microscope (SEM). The two prototype cements exhibited changes in their internal chemistry with no changes in surface characteristics. Since the changes observed were mostly sub-surface evaluation of surface characteristics of cement may not be sufficient in the determination of chemical changes occurring. - Research Highlights: → An acidic environment affects modified fast setting calcium silicate-based cements. → No surface changes are observed in acidic environment. → An acidic environment causes sub-surface changes in the material chemistry which are only visible in fractured specimens. → A combination of techniques is necessary in order to evaluate the chemical changes occurring.

  9. In vitro osteoblast-like and endothelial cells' response to calcium silicate/calcium phosphate cement

    International Nuclear Information System (INIS)

    This study aims to investigate the interaction between calcium silicate/calcium phosphate cement (CS/CPC) and osteogenesis, in particular the in vitro osteoblast-like and endothelial cells' response to CS/CPC. The effect of CS/CPC on cell attachment, proliferation and differentiation of murine osteoblast-like cell MC3T3-E1, as well as the influence on the cell attachment and proliferation of human umbilical vein endothelial cell (HUVEC), was studied in detail. Our results indicated that CS/CPC exhibited excellent biocompatibility to the osteoblast-like cells. Moreover, the morphology and cytoskeleton organization of MC3T3-E1 cultured on the CS/CPC disks suggested that CS/CPC induced better cell adhesion and cell spreading. Simultaneously, cell proliferation and alkaline phosphatase (ALP) activity of MC3T3-E1 were significantly improved after 3 and 7 days of culture on CS/CPC disks in comparison with CPC disks. Additionally, on CS/CPC disks, HUVEC attached well on day 1 and cell proliferation was also greatly enhanced by day 7. Collectively, these results suggest that the introduction of calcium silicate may improve the cell response involved in the osteogenesis and thus may be beneficial to further modify CPC as a better bone repairing material.

  10. Calcium Silicate-Based Cements Associated with Micro- and Nanoparticle Radiopacifiers: Physicochemical Properties and Bioactivity

    OpenAIRE

    BOSSO-MARTELO, Roberta; Juliane Maria GUERREIRO-TANOMARU; Viapiana, Raqueli; Berbert, Fábio Luis Camargo Vilella; Basso Bernardi, Maria Inês; Tanomaru-Filho, Mario

    2015-01-01

    Objective. The aim of this study was to evaluate the physicochemical properties and bioactivity of two formulations of calcium silicate-based cements containing additives (CSCM) or resin (CSCR), associated with radiopacifying agents zirconium oxide (ZrO2) and niobium oxide (Nb2O5) as micro- and nanoparticles; calcium tungstate (CaWO4); and bismuth oxide (Bi2O3). MTA Angelus was used as control. Methods. Surface features and bioactivity were evaluated by scanning electron microscopy and the ch...

  11. Phase transformations, microstructure formation and in vitro osteoblast response in calcium silicate/brushite cement composites.

    Science.gov (United States)

    Sopcak, T; Medvecky, L; Giretova, M; Kovalcikova, A; Stulajterova, R; Durisin, J

    2016-01-01

    Self-setting simple calcium silicate/brushite (B) biocements with various Ca/P ratios were prepared by mutual mixing of both monocalcium silicate hydrate (CSH) or β-wollastonite (woll) powders with B and the addition of 2 wt% NaH2PO4 solution as a hardening liquid. The phase composition of the final composites and the texture of the surface calcium phosphate/silica layer were controlled by the starting Ca/P ratio in composites and the pH during setting. It was verified that the presence of continuous bone-like calcium phosphate coating on the surface of the samples was not essential for in vitro osteoblast proliferation. The nanocrystalline calcium deficient hydroxyapatite and amorphous silica were found as the main setting products in composite mixtures with a Ca/P ratio close to the region of the formation of deficient hydroxyapatite-like calcium phosphates. No CSH phase with a lower Ca/Si ratio was identified after transformation. The results confirmed a small effect of the monocalcium silicate addition on the compressive strength (CS) of cements up to 30 wt% (around 20-25 MPa) and a significant rise of the value in 50 woll/B cement (65 MPa). The final setting times of the cement composites varied between 5 and 43 min depending on the P/L ratio and the type of monocalcium silicate phase in the cement mixture. 10CSH/B and 50 woll/B cements with different textures but free of both the needle-like and perpendicularly-oriented hydroxyapatite particles on the surface of the samples had low cytotoxicity. PMID:27509265

  12. Physical characteristics, antimicrobial and odontogenesis potentials of calcium silicate cement containing hinokitiol.

    Science.gov (United States)

    Huang, Ming-Hsien; Shen, Yu-Fang; Hsu, Tuan-Ti; Huang, Tsui-Hsien; Shie, Ming-You

    2016-08-01

    Hinokitiol is a natural material and it has antibacterial and anti-inflammatory effects. The purpose of this study was to evaluate the material characterization, cell viability, antibacterial and anti-inflammatory abilities of the hinokitiol-modified calcium silicate (CS) cement as a root end filling material. The setting times, diametral tensile strength (DTS) values and XRD patterns of CS cements with 0-10mM hinokitiol were examined. Then, the antibacterial effect and the expression levels of cyclooxygenase 2 (COX-2) and interleukin-1 (IL-1) of the hinokitiol-modified CS cements were evaluated. Furthermore, the cytocompatibility, the expression levels of the markers of odontoblastic differentiation, mineralized nodule formation and calcium deposition of human dental pulp cells (hDPCs) cultured on hinokitiol-modified CS cements were determined. The hinokitiol-modified CS cements had better antibacterial and anti-inflammatory abilities and cytocompatibility than non-modified CS cements. Otherwise, the hinokitiol-modified CS cements had suitable setting times and better odontoblastic potential of hDPCs. Previous report pointed out that the root-end filling materials may induce inflammatory cytokines reaction. In our study, hinokitiol-modified CS cements not only inhibited the expression level of inflammatory cytokines, but also had better cytocompatibility, antimicrobial properties and active ability of odontoblastic differentiation of hDPCs. Therefore, the hinokitiol-modified CS cement may be a potential root end filling material for clinic. PMID:27157721

  13. Cytotoxicity and genotoxicity of calcium silicate-based cements on an osteoblast lineage

    Directory of Open Access Journals (Sweden)

    Ana Lívia GOMES-CORNÉLIO

    2016-01-01

    Full Text Available Abstract Several calcium silicate-based biomaterials have been developed in recent years, in addition to Mineral Trioxide Aggregate (MTA. The aim of this study was to evaluate the cytotoxicity, genotoxicity and apoptosis/necrosis in human osteoblast cells (SAOS-2 of pure calcium silicate-based cements (CSC and modified formulations: modified calcium silicate-based cements (CSCM and three resin-based calcium silicate cements (CSCR1 (CSCR 2 (CSCR3. The following tests were performed after 24 hours of cement extract exposure: methyl-thiazolyl tetrazolium (MTT, apoptosis/necrosis assay and comet assay. The negative control (CT- was performed with untreated cells, and the positive control (CT+ used hydrogen peroxide. The data for MTT and apoptosis were submitted to analysis of variance and Bonferroni’s posttest (p < 0.05, and the data for the comet assay analysis, to the Kruskal-Wallis and Dunn tests (p < 0.05. The MTT test showed no significant difference among the materials in 2 mg/mL and 10 mg/mL concentrations. CSCR3 showed lower cell viability at 10 mg/mL. Only CSC showed lower cell viability at 50 mg/mL. CSCR1, CSCR2 and CSCR3 showed a higher percentage of initial apoptosis than the control in the apoptosis test, after 24 hours exposure. The same cements showed no genotoxicity in the concentration of 2 mg/mL, with the comet assay. CSC and CSCR2 were also not genotoxic at 10 mg/mL. All experimental materials showed viability with MTT. CSC and CSCR2 presented a better response to apoptosis and genotoxicity evaluation in the 10 mg/mL concentration, and demonstrated a considerable potential for use as reparative materials.

  14. Analysis of the color alteration and radiopacity promoted by bismuth oxide in calcium silicate cement

    Directory of Open Access Journals (Sweden)

    Marina Angelica Marciano

    2013-07-01

    Full Text Available The aim of the study was to determine if the increase in radiopacity provided by bismuth oxide is related to the color alteration of calcium silicate-based cement. Calcium silicate cement (CSC was mixed with 0%, 15%, 20%, 30% and 50% of bismuth oxide (BO, determined by weight. Mineral trioxide aggregate (MTA was the control group. The radiopacity test was performed according to ISO 6876/2001. The color was evaluated using the CIE system. The assessments were performed after 24 hours, 7 and 30 days of setting time, using a spectrophotometer to obtain the ΔE, Δa, Δb and ΔL values. The statistical analyses were performed using the Kruskal-Wallis/Dunn and ANOVA/Tukey tests (p 3 mm equivalent of Al. The MTA group was statistically similar to the CSC / 30% BO group (p > 0.05. In regard to color, the increase of bismuth oxide resulted in a decrease in the ΔE value of the calcium silicate cement. The CSC group presented statistically higher ΔE values than the CSC / 50% BO group (p < 0.05. The comparison between 24 hours and 7 days showed higher ΔE for the MTA group, with statistical differences for the CSC / 15% BO and CSC / 50% BO groups (p < 0.05. After 30 days, CSC showed statistically higher ΔE values than CSC / 30% BO and CSC / 50% BO (p < 0.05. In conclusion, the increase in radiopacity provided by bismuth oxide has no relation to the color alteration of calcium silicate-based cements.

  15. Apatite formation on bioactive calcium-silicate cements for dentistry affects surface topography and human marrow stromal cells proliferation.

    Science.gov (United States)

    Gandolfi, Maria Giovanna; Ciapetti, Gabriela; Taddei, Paola; Perut, Francesca; Tinti, Anna; Cardoso, Marcio Vivan; Van Meerbeek, Bart; Prati, Carlo

    2010-10-01

    The effect of ageing in phosphate-containing solution of bioactive calcium-silicate cements on the chemistry, morphology and topography of the surface, as well as on in vitro human marrow stromal cells viability and proliferation was investigated. A calcium-silicate cement (wTC) mainly based on dicalcium-silicate and tricalcium-silicate was prepared. Alpha-TCP was added to wTC to obtain wTC-TCP. Bismuth oxide was inserted in wTC to prepare a radiopaque cement (wTC-Bi). A commercial calcium-silicate cement (ProRoot MTA) was tested as control. Cement disks were aged in DPBS for 5 h ('fresh samples'), 14 and 28 days, and analyzed by ESEM/EDX, SEM/EDX, ATR-FTIR, micro-Raman techniques and scanning white-light interferometry. Proliferation, LDH release, ALP activity and collagen production of human marrow stromal cells (MSC) seeded for 1-28 days on the cements were evaluated. Fresh samples exposed a surface mainly composed of calcium-silicate hydrates CSH (from the hydration of belite and alite), calcium hydroxide, calcium carbonate, and ettringite. Apatite nano-spherulites rapidly precipitated on cement surfaces within 5 h. On wTC-TCP the Ca-P deposits appeared thicker than on the other cements. Aged cements showed an irregular porous calcium-phosphate (Ca-P) coating, formed by aggregated apatite spherulites with interspersed calcite crystals. All the experimental cements exerted no acute toxicity in the cell assay system and allowed cell growth. Using biochemical results, the scores were: fresh cements>aged cements for cell proliferation and ALP activity (except for wTC-Bi), whereas fresh cementscements for collagen synthesis. Summarizing (1) non-aged cements showed higher cell proliferation than aged cements, probably favoured by the presence of Si-OH gel and the early formation of apatite nano-spherulites; (2) the alpha-TCP doped cement aged for 28 days displayed the highest bioactivity and cell proliferation; (3) the deleterious effect of bismuth on cell

  16. Apatite precipitation on a novel fast-setting calcium silicate cement containing fluoride

    Science.gov (United States)

    Ranjkesh, Bahram; Chevallier, Jacques; Salehi, Hamideh; Cuisinier, Frédéric; Isidor, Flemming; Løvschall, Henrik

    2016-01-01

    Abstract Aim: Calcium silicate cements are widely used in endodontics. Novel fast-setting calcium silicate cement with fluoride (Protooth) has been developed for potential applications in teeth crowns including cavity lining and cementation. Objective: To evaluate the surface apatite-forming ability of Protooth compositions as a function of fluoride content and immersion time in phosphate-buffered saline (PBS). Material and methods: Three cement compositions were tested: Protooth (3.5% fluoride and 10% radiocontrast), ultrafast Protooth (3.5% fluoride and 20% radiocontrast), and high fluoride Protooth (15% fluoride and 25% radiocontrast). Powders were cap-mixed with liquid, filled to the molds and immersed in PBS. Scanning electron microscopy, energy dispersive X-ray analysis, and Raman spectroscopy were used to characterize the precipitations morphology and composition after 1, 7, 28, and 56 days. Apatite/belite Raman peak height indicated the apatite thickness. Results: Spherical calcium phosphate precipitations with acicular crystallites were formed after 1-day immersion in PBS and Raman spectra disclosed the phosphate band at 965 cm−1, supporting the apatite formation over Protooth compositions. The apatite deposition continued and more voluminous precipitations were observed after 56 days over the surface of all cements. Raman bands suggested the formation of β-type carbonated apatite over Protooth compositions. High fluoride Protooth showed the most compact deposition with significantly higher apatite/belite ratio compared to Protooth and ultrafast Protooth after 28 and 56 days. Conclusions: Calcium phosphate precipitations (apatite) were formed over Protooth compositions after immersion in PBS with increasing apatite formation as a function of time. High fluoride Protooth exhibited thicker apatite deposition. PMID:27335901

  17. Preparation and in vitro evaluation of strontium-doped calcium silicate/gypsum bioactive bone cement

    International Nuclear Information System (INIS)

    The combination of two or more bioactive components with different biodegradability could cooperatively improve the physicochemical and biological performances of the biomaterials. Here we explore the use of α-calcium sulfate hemihydrate (α-CSH) and calcium silicate with and without strontium doping (Sr-CSi, CSi) to fabricate new bioactive cements with appropriate biodegradability as bone implants. The cements were fabricated by adding different amounts (0–35 wt%) of Sr-CSi (or CSi) into the α-CSH-based pastes at a liquid-to-solid ratio of 0.4. The addition of Sr-CSi into α-CSH cements not only led to a pH rise in the immersion medium, but also changed the surface reactivity of cements, making them more bioactive and therefore promoting apatite mineralization in simulated body fluid (SBF). The impact of additives on long-term in vitro degradation was evaluated by soaking the cements in Tris buffer, SBF, and α-minimal essential medium (α-MEM) for a period of five weeks. An addition of 20% Sr-CSi to α-CSH cement retarded the weight loss of the samples to 36% (in Tris buffer), 43% (in SBF) and 54% (in α-MEM) as compared with the pure α-CSH cement. However, the addition of CSi resulted in a slightly faster degradation in comparison with Sr-CSi in these media. Finally, the in vitro cell-ion dissolution products interaction study using human fetal osteoblast cells demonstrated that the addition of Sr-CSi improved cell viability and proliferation. These results indicate that tailorable bioactivity and biodegradation behavior can be achieved in gypsum cement by adding Sr-CSi, and such biocements will be of benefit for enhancing bone defect repair. (paper)

  18. Silicate anion structural change in calcium silicate hydrate gel on dissolution of hydrated cement

    International Nuclear Information System (INIS)

    High pH conditions of aqueous solutions in a radioactive waste repository can be brought about by dissolution of cementitious materials. In order to clarify the mechanisms involved in maintaining this high pH for long time, we investigated the dissolution phenomena of OPC hydrate. In the present research, leaching tests on powdered cement hydrates were conducted by changing the ratio of mass of leaching water to mass of OPC hydrate (liquid/solid ratio) from 10 - 2,000 (wt/wt). Ordinary Portland Cement hydrate was contacted with deionized water and placed in a sealed bottle. After a predetermined period, the solid was separated from the solution. From the results of XRD analysis on the solid phase and the Ca concentration in the aqueous phase, it was confirmed that Ca(OH)2 was preferentially dissolved when the liquid/solid ratio was 10 or 100 (wt/wt), and that C-S-H gel as well as Ca(OH)2 were dissolved when the liquid/solid ratio was 500 (wt/wt) or larger. 29Si-NMR results showed that the silicate anion chain of the C-S-H gel became longer when the liquid/solid ratio was 500 (wt/wt) or greater. This indicates that leaching of OPC hydrate results in a structural change of C-S-H gel. (author)

  19. Improvement of in vitro physicochemical properties and osteogenic activity of calcium sulfate cement for bone repair by dicalcium silicate

    International Nuclear Information System (INIS)

    Highlights: • Dicalcium silicate can improve osteogenic activity of calcium sulfate cement. • The higher the calcium sulfate content, the shorter the setting time in the composite cement. • The results were useful for designing calcium-based cement with optimal properties. -- Abstract: An ideal bone graft substitute should have the same speed of degradation as formation of new bone tissue. To improve the properties of calcium sulfate hemihydrate (CSH) featured for its rapid resorption, a low degradation material of dicalcium silicate (DCS) was added to the CSH cement. This study examined the effect of DCS (20, 40, 60 and 80 wt%) on the in vitro physicochemical properties and osteogenic activities of the calcium-based composite cements. The diametral tensile strength, porosity and weight loss of the composite cements were evaluated before and after soaking in a simulated body fluid (SBF). The osteogenic activities, such as proliferation, differentiation and mineralization, of human mesenchymal stem cells (hMSCs) seeded on cement surfaces were also examined. As a result, the greater the DCS amount, the higher the setting time was in the cement. Before soaking in SBF, the diametral tensile strength of the composite cements was decreased due to the introduction of DCS. On 180-day soaking, the composite cements containing 20, 40, 60 and 80 wt% DCS lost 80%, 69%, 61% and 44% in strength, respectively. Regarding in vitro bioactivity, the DCS-rich cements were covered with clusters of apatite spherulites after soaking for 7 days, while there was no formation of apatite spherulites on the CSH-rich cement surfaces. The presence of DCS could reduce the degradation of the CSH cements, as evidenced in the results of weight loss and porosity. More importantly, DCS may promote effectively the cell proliferation, proliferation and mineralization. The combination of osteogenesis of DCS and degradation of CSH made the calcium-based composite cements an attractive choice for

  20. Push-out bond strength of CPP-ACP-modified calcium silicate-based cements.

    Science.gov (United States)

    Dawood, Alaa E; Manton, David J; Parashos, Peter; Wong, Rebecca H k; Palamara, Joseph E A; Reynolds, Eric C

    2015-01-01

    This study evaluated the push-out bond strength of 0%, 0.5%, 1.0%, 2.0% and 3.0% (w/w) casein phosphopeptide-amorphous calcium phosphate (CPP-ACP)-modified calcium silicate-based cements (CSCs). The push-out bond strength of a trial MTA was also compared with two CSCs (Biodentine(™) and Angelus(®) MTA). Three hundred 1 mm thick horizontal root sections were prepared from 60 singlerooted human teeth. The canal space of each section was enlarged and filled with the cements. The sections were stored in a phosphate buffer solution. After incubation for 2 months, the push-out bond strength was measured and the data were analyzed using one way analysis of variance followed by Tukey's test. The addition of CPP-ACP to the test cements increased the push-out bond strength (p<0.05). The push-out bond strength of Biodentine(™) was higher than the other cements (p<0.05). There was no statistically significant difference between Angelus(®) MTA and the trial MTA with most of CPP-ACP concentrations. PMID:26235714

  1. Development of a novel fluorapatite-forming calcium phosphate cement with calcium silicate: in vitro and in vivo characteristics.

    Science.gov (United States)

    Suzuki, Yusuke; Hayashi, Makoto; Yasukawa, Takuya; Kobayashi, Hiroshi; Makino, Kosuke; Hirano, Yoriyuki; Takagi, Shozo; Chow, Laurence C; Ogiso, Bunnai

    2015-01-01

    Aim of this study was to develop a novel fluorapatite-forming calcium phosphate cement (FA-CPC) with tricalcium silicate (TCS) for endodontic applications and to examine its in vitro and in vivo characteristics. The FA-CPC powder consisted of 62.8% CaHPO4, 30.8% CaCO3, and 6.4% NaF. One part of TCS was combined with 9 parts of FA-CPC powder (FA-CPC with TCS). A 1.5 M phosphate solution was used as cement liquid. Setting time (ST), diametral tensile strength (DTS), phase composition by X-ray diffraction (XRD), and cement alkalinity were analyzed. Cement biocompatibility was assessed using rat subcutaneous model. Cement ST was 10.3±0.6 min and DTS was 3.89±0.76 MPa. XRD patterns showed that highly crystalline apatitic material was the only significant phase present and pH value was approximate 11.0. FA-CPC with TCS demonstrated similar biocompatibility as that of mineral trioxide aggregate control. These results suggest that FA-CPC with TCS may be useful for endodontic applications. PMID:25740309

  2. In Vitro Cytotoxicity of Calcium Silicate-Based Endodontic Cement as Root-End Filling Materials.

    Science.gov (United States)

    Küçükkaya, Selen; Görduysus, Mehmet Ömer; Zeybek, Naciye Dilara; Müftüoğlu, Sevda Fatma

    2016-01-01

    The aim of this study was to evaluate the cytotoxicity of three types of calcium silicate-based endodontic cement after different incubation periods with human periodontal ligament fibroblasts. Human periodontal ligament fibroblasts were cultured from extracted third molars and seeded in 96-well plates. MTA, calcium enriched mixture (CEM) cement, and Biodentine were prepared and added to culture insert plates which were immediately placed into 96-well plates containing cultured cells. After incubation periods of 24, 48, and 72 hours, cell viability was determined with WST-1 assay. Data were analysed statistically by ANOVA with repeated measures and Bonferroni tests. There was no significant difference in cell viability amongst the test materials after each incubation period (P > 0.05). MTA and CEM presented more than 90% cell viability after 24 and 48 hours of incubation and showed statistically significant decrease in cell viability after 72 hours of incubation (P Biodentine showed significantly less cell viability (73%) after 24 hours of incubation, whereas more than 90% cell viability was seen after 48 and 72 hours of incubation (P Biodentine and CEM can be considered as alternative materials for root-end surgery procedures. PMID:26904364

  3. Mechanistic study and modeling of radionuclides retention by the hydrated calcium silicates (HCS) of cements

    International Nuclear Information System (INIS)

    This work attempts to investigate the modelling of radioisotopes (Cs+, Pb2+, Eu3+) immobilization in cement matrix, in the frame of the design of engineered barrier of a deep radwaste repository. The model development concept consists of three major steps: - surface chemistry modelling of the calcium silicate hydrate CSH, used to simulate hydrated cement behaviour; - solid analysis of the batch sorption experiments: identification of the uptake mechanism; - both previous steps are used, with isotherm data, in the modelling of the radioisotopes immobilization in the CSH matrix. Final results: (all modelling are available for all the range of studied Ca/Si ratios and have been validated with predictive calculations). - A thermodynamic modelling of the CSH surface chemistry has been developed. The labile calcium and proton sorption constants on silanol sites (>SiOH) have been extracted. - Cs+ is sorbed on two sites. The silanol site (weak site) has a high site density (10 sites.nm-2), which accounts for the CSH unsaturation in high [CS+]. A strong site is also identified. - Pb2+ immobilization in CSH matrix is modelled with surface equilibria and solubility equilibrium. - Eu3+ fixation has been investigated with solid analysis: Site-Selective anti Time-Resolved Luminescence Spectroscopy, XPS and SEM-EDS. Eu3+ thus does not precipitate in CSH water but is sorbed on the CSH surface (high hydroxylated environment). Europium is also (minority site) inserted in the CSH framework. (author)

  4. A Comprehensive Study of Osteogenic Calcium Phosphate Silicate Cement: Material Characterization and In Vitro/In Vivo Testing.

    Science.gov (United States)

    Gong, Tianxing; Wang, Zhiqin; Zhang, Yixi; Zhang, Yubiao; Hou, Mingxiao; Liu, Xinwei; Wang, Yu; Zhao, Lejun; Ruse, N Dorin; Troczynski, Tom; Häfeli, Urs O

    2016-02-18

    Vertebral compression fractures can be successfully restored by injectable bone cements. Here the as-yet unexplored in vitro cytotoxicity, in vivo biodegradation, and osteoconductivity of a new calcium phosphate silicate cements (CPSC) are studied, where monocalcium phosphate (MCP; 5, 10, and 15 wt%) is added to calcium silicate cement (CSC). Setting rate and compressive strength of CPSC decrease with the addition of MCP. The crystallinity, microstructure, and porosity of hardened CPSC are evaluated by X-ray diffractometer, Fourier transform infrared spectroscopy, and microcomputed tomography (CT). It is found that MCP reacts with calcium hydroxide, one of CSC hydration products, to precipitate apatite. While the reaction accelerates the hydration of CSC, the formation of calcium silicate hydrate gel is disturbed and highly porous microstructures form, resulting in weaker compressive strength. In vitro studies demonstrate that CPSC is noncytotoxic to osteoblast cells and promotes their proliferation. In the rabbit tibia implantation model, clinical X-ray and CT scans demonstrate that CPSC biodegrades slower and osseointegrates better than clinically used calcium phosphate cement (CPC). Histological studies demonstrate that CPSC is osteoconductive and induces higher bone formation than CPC, a finding that might warrant future clinical studies. PMID:26677175

  5. In vitro osteoblast-like and endothelial cells' response to calcium silicate/calcium phosphate cement

    Energy Technology Data Exchange (ETDEWEB)

    Zhao Qinghui; Qian Jiangchao [State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237 (China); Zhou Huanjun; Yuan Yuan; Mao Yuhao; Liu Changsheng, E-mail: jiangchaoqian@ecust.edu.c, E-mail: csliu@sh163.ne [Engineering Research Center for Biomedical Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237 (China)

    2010-06-01

    This study aims to investigate the interaction between calcium silicate/calcium phosphate cement (CS/CPC) and osteogenesis, in particular the in vitro osteoblast-like and endothelial cells' response to CS/CPC. The effect of CS/CPC on cell attachment, proliferation and differentiation of murine osteoblast-like cell MC3T3-E1, as well as the influence on the cell attachment and proliferation of human umbilical vein endothelial cell (HUVEC), was studied in detail. Our results indicated that CS/CPC exhibited excellent biocompatibility to the osteoblast-like cells. Moreover, the morphology and cytoskeleton organization of MC3T3-E1 cultured on the CS/CPC disks suggested that CS/CPC induced better cell adhesion and cell spreading. Simultaneously, cell proliferation and alkaline phosphatase (ALP) activity of MC3T3-E1 were significantly improved after 3 and 7 days of culture on CS/CPC disks in comparison with CPC disks. Additionally, on CS/CPC disks, HUVEC attached well on day 1 and cell proliferation was also greatly enhanced by day 7. Collectively, these results suggest that the introduction of calcium silicate may improve the cell response involved in the osteogenesis and thus may be beneficial to further modify CPC as a better bone repairing material.

  6. Nanostructural Deformation Analysis of Calcium Silicate Hydrate in Portland Cement Paste by Atomic Pair Distribution Function

    Directory of Open Access Journals (Sweden)

    Hiroshi Suzuki

    2016-01-01

    Full Text Available The deformation of nanostructure of calcium silicate hydrate (C-S-H in Portland cement (PC paste under compression was characterized by the atomic pair distribution function (PDF, measured using synchrotron X-ray diffraction. The PDF of the PC paste exhibited a unique deformation behavior for a short-range order below 2.0 nm, close to the size of the C-S-H globule, while the deformation for a long-range order was similar to that of a calcium hydroxide phase measured by Bragg peak shift. The compressive deformation of the C-S-H nanostructure was comprised of three stages with different interactions between globules. This behavior would originate from the granular nature of C-S-H, which deforms with increasing packing density by slipping the interfaces between globules, rearranging the overall C-S-H nanostructure. This new approach will lead to increasing applications of the PDF technique to understand the deformation mechanism of C-S-H in PC-based materials.

  7. Fluoride-containing nanoporous calcium-silicate MTA cements for endodontics and oral surgery: Early fluorapatite formation in a phosphate-containing solution

    OpenAIRE

    Gandolfi, M.G.; Taddei, P.; Siboni, F.; Modena, E.; Ginebra Molins, Maria Pau; Prati, Claudio

    2011-01-01

    Gandolfi MG, Taddei P, Siboni F, Modena E, Ginebra MP, Prati C. Fluoride-containing nanoporous calcium-silicate MTA cements for endodontics and oral surgery: early fluorapatite formation in a phosphate-containing solution. International Endodontic Journal, 44, 938–949, 2011. Aim To test the chemical–physical properties and apatite-forming ability of experimental fluoride-doped calcium silicate cements designed to create novel bioactive materials for use in endodontics ...

  8. Intrinsic differences in atomic ordering of calcium (alumino)silicate hydrates in conventional and alkali-activated cements

    Energy Technology Data Exchange (ETDEWEB)

    White, Claire E., E-mail: whitece@princeton.edu [Department of Civil and Environmental Engineering, Princeton University, Princeton (United States); Andlinger Center for Energy and the Environment, Princeton University, Princeton (United States); Lujan Neutron Scattering Center, Los Alamos National Laboratory, Los Alamos (United States); Physics and Chemistry of Materials, Los Alamos National Laboratory, Los Alamos (United States); Daemen, Luke L.; Hartl, Monika; Page, Katharine [Lujan Neutron Scattering Center, Los Alamos National Laboratory, Los Alamos (United States)

    2015-01-15

    The atomic structures of calcium silicate hydrate (C–S–H) and calcium (–sodium) aluminosilicate hydrate (C–(N)–A–S–H) gels, and their presence in conventional and blended cement systems, have been the topic of significant debate over recent decades. Previous investigations have revealed that synthetic C–S–H gel is nanocrystalline and due to the chemical similarities between ordinary Portland cement (OPC)-based systems and low-CO{sub 2} alkali-activated slags, researchers have inferred that the atomic ordering in alkali-activated slag is the same as in OPC–slag cements. Here, X-ray total scattering is used to determine the local bonding environment and nanostructure of C(–A)–S–H gels present in hydrated tricalcium silicate (C{sub 3}S), blended C{sub 3}S–slag and alkali-activated slag, revealing the large intrinsic differences in the extent of nanoscale ordering between C–S–H derived from C{sub 3}S and alkali-activated slag systems, which may have a significant influence on thermodynamic stability, and material properties at higher length scales, including long term durability of alkali-activated cements.

  9. Intrinsic differences in atomic ordering of calcium (alumino)silicate hydrates in conventional and alkali-activated cements

    International Nuclear Information System (INIS)

    The atomic structures of calcium silicate hydrate (C–S–H) and calcium (–sodium) aluminosilicate hydrate (C–(N)–A–S–H) gels, and their presence in conventional and blended cement systems, have been the topic of significant debate over recent decades. Previous investigations have revealed that synthetic C–S–H gel is nanocrystalline and due to the chemical similarities between ordinary Portland cement (OPC)-based systems and low-CO2 alkali-activated slags, researchers have inferred that the atomic ordering in alkali-activated slag is the same as in OPC–slag cements. Here, X-ray total scattering is used to determine the local bonding environment and nanostructure of C(–A)–S–H gels present in hydrated tricalcium silicate (C3S), blended C3S–slag and alkali-activated slag, revealing the large intrinsic differences in the extent of nanoscale ordering between C–S–H derived from C3S and alkali-activated slag systems, which may have a significant influence on thermodynamic stability, and material properties at higher length scales, including long term durability of alkali-activated cements

  10. Reproducibility of the uptake of U(VI) onto degraded cement pastes and calcium silicate hydrate phases

    International Nuclear Information System (INIS)

    The U(VI) uptake in degraded cement pastes was undertaken in the laboratories of CEA/L3MR and SUBATECH in order to check the reproducibility of the study. Two well hydrated cement pastes, CEM I (ordinary portland cement, OPC) and CEM V (blast furnace slag (BFS) and fly ash added to OPC) were degraded using similar protocols. Equilibrium solutions and solid materials were characterised for three degradation states for each paste. All samples are free of portlandite and the pH of the equilibrated cement solutions vary in the range 9.8-12.2. Three calcium silicate hydrate phases (C-S-H) were synthesised in order to compare the sorption properties of degraded cement pastes and of hydrate phases in similar pH conditions. In order to avoid precipitation processes, the operational solubility limit was evaluated before batch experiments. These solubility values vary significantly in the pH range [9-13] with a 2.4 x 10-7 mol L-1 minimum at pH close to 10.5. In batch sorption experiments, the distribution ratio Rd values are high: 3 x 104 - 1.5 x 105 mL g-1. The uptake of U(VI) increases when comparing the least and the most degraded cement pastes whereas the initial composition of cement has relatively insensitive effect. Sorption isotherms, expressed as a log [U(VI)solid]/log[U(VI)solution] plots are linear. A slope of 1 is calculated indicating the predominance of sorption processes. As sorption and desorption values are close, the uptake mechanism seems reversible. The Rd values measured in C-S-H suspensions are in good agreement with Rd values of degraded cement pastes, and C-S-H materials could be one of the cementitious phases which control U(VI) uptake in cement pastes. (orig.)

  11. Calcium-aluminum-silicate-hydrate "cement" phases and rare Ca-zeolite association at Colle Fabbri, Central Italy

    Science.gov (United States)

    Stoppa, F.; Scordari, F.; Mesto, E.; Sharygin, V.; Bortolozzi, G.

    2010-06-01

    Very high temperature, Ca-rich alkaline magma intruded an argillite formation at Colle Fabbri, Central Italy, producing cordierite-tridymite metamorphism in the country rocks. An intense Ba-rich sulphate-carbonate-alkaline hydrothermal plume produced a zone of mineralization several meters thick around the igneous body. Reaction of hydrothermal fluids with country rocks formed calcium-silicate-hydrate (CSH), i.e., tobermorite-afwillite-jennite; calcium-aluminum-silicate-hydrate (CASH) — "cement" phases - i.e., thaumasite, strätlingite and an ettringite-like phase and several different species of zeolites: chabazite-Ca, willhendersonite, gismon-dine, three phases bearing Ca with the same or perhaps lower symmetry of phillipsite-Ca, levyne-Ca and the Ca-rich analogue of merlinoite. In addition, apophyllite-(KF) and/or apophyllite-(KOH), Ca-Ba-carbonates, portlandite and sulphates were present. A new polymorph from the pyrrhotite group, containing three layers of sphalerite-type structure in the unit cell, is reported for the first time. Such a complex association is unique. Most of these minerals are specifically related to hydration processes of: (1) pyrometamorphic metacarbonate/metapelitic rocks (natural analogues of cement clinkers); (2) mineralization between intrusive stocks and slates; and (3) high-calcium, alkaline igneous rocks such as melilitites and foidites as well as carbonatites. The Colle Fabbri outcrop offers an opportunity to study in situ complex crystalline overgrowth and specific crystal chemistry in mineral phases formed in igneous to hydrothermal conditions.

  12. In vivo evaluation of the effects of hydraulic calcium silicate dental cements on plasma and liver aluminium levels in rats.

    Science.gov (United States)

    Demirkaya, Kadriye; Can Demirdöğen, Birsen; Öncel Torun, Zeynep; Erdem, Onur; Çetinkaya, Serdar; Akay, Cemal

    2016-02-01

    Our aim was to test whether the presence of three hydraulic calcium silicate dental cements--MTA Angelus, MTA Fillapex, and Theracal LC--in the dental extraction socket of an in vivo model, would affect the levels of aluminium (Al) in the plasma and liver. Following anesthesia, the right upper incisor of each male Wistar albino rat was extracted and polyethylene tubes filled with MTA Angelus, MTA Fillapex, or Theracal LC were inserted into the depth of the extraction socket and gingival tissue was sutured. The rats were killed 7, 30, or 60 d after the operation. Blood and liver samples were obtained from the rats before they were killed, and the levels of Al were measured by atomic absorption spectrometry. Plasma Al levels were higher in the rats in which the mineral trioxide aggregate (MTA) cements were implanted, especially MTA Angelus and MTA Fillapex, compared with control rats. In liver samples, however, the differences in Al level were not statistically significant. Our results show that Al might have been released into the circulation from the three dental cements tested, especially MTA Angelus and MTA Fillapex. Further research should be carried out on the possible biological effects of Al liberated from dental cements. PMID:26706154

  13. Push-out bond strength of MTA HP, a new high-plasticity calcium silicate-based cement.

    Science.gov (United States)

    Silva, Emmanuel Jnl; Carvalho, Nancy Kudsi; Zanon, Mayara; Senna, Plínio Mendes; DE-Deus, Gustavo; Zuolo, Mário Luis; Zaia, Alexandre Augusto

    2016-06-14

    This study was designed to investigate the resistance to dislodgment provided by MTA HP, a new high-plasticity calcium silicate-based cement. Biodentine and White MTA Angelus were used as reference materials for comparison. Three discs 1 ± 0.1 mm thick were obtained from the middle third of the roots of 5 maxillary canines. Three 0.8-mm-wide holes were drilled on the axial surface of each root disc. Standardized irrigation was performed. Then the holes were dried with paper points and filled with one of the three tested cements. The filled dental slices were immersed in a phosphate-buffered saline (PBS) solution (pH 7.2) for 7 days before the push-out assessment. The Kruskal-Wallis test was applied to assess the effect of each endodontic cement on the push-out bond strength. Mann-Whitney with Bonferroni correction was used to isolate the differences. The alpha-type error was set at 0.05. All specimens had measurable push-out values and no premature failure occurred. There were significant differences among the materials (p <0.05). The Biodentine specimens had the highest push-out bond strength values (p < 0.05). MTA HP had significantly higher bond strength than White MTA (p < 0.05). MTA HP showed better push-out bond strength than its predecessor, White MTA; however, Biodentine had higher dislodgment resistance than both MTA formulations. PMID:27305515

  14. Interaction of calcium silicate hydrates (C-S-H), the main components of cement, with alkaline chlorides, analogy with clays

    International Nuclear Information System (INIS)

    This work, belonging to a more general study on the structure and reactivity of cement, deals with the experimental and theoretical analysis of the interaction of alkaline chlorides with calcium silicate hydrates (C-S-H), the main components of cement paste. The interaction of alkaline cations with C-S-H is interfacial, involving both electrostatic and surface complexation mechanisms. The C-S-H surface is constituted of silanol sites, partially dissociated due to the high pH of the interstitial solution. The calcium ions, present in large amounts in the equilibrium solution of C-S-H, constitute potential determining ions for the C-S-H surface. The alkaline ions seem to compete with calcium for the same surface sites. The adsorption isotherms show that caesium presents a better affinity than sodium and lithium for the C-S-H surface. Moreover, solid-state NMR suggests that caesium forms with the surface sites inner-sphere complexes, whereas sodium seems to keep its hydration sphere. These results are in agreement with zeta potential measurements, which let suppose a specific adsorption of caesium ions, and an indifferent behaviour of both other alkaline ions. A model for the C-S-H surface was proposed, from the electric double layer model, and mass action laws expressing the complexation of the different ionic species with the silanol sites. The whole study relies on a structural analogy with smectites, some clays presenting well-known cationic adsorption properties. The structural similarity between both minerals is enhanced by some similarities of reactivity, though significant behaviour differences could also be noted. (author)

  15. Sustainable Nanopozzolan Modified Cement: Characterizations and Morphology of Calcium Silicate Hydrate during Hydration

    Directory of Open Access Journals (Sweden)

    N. Mohamed Sutan

    2015-01-01

    Full Text Available There are environmental and sustainable benefits of partially replacing cement with industrial by-products or synthetic materials in cement based products. Since microstructural behaviours of cement based products are the crucial parameters that govern their sustainability and durability, this study investigates the microstructural comparison between two different types of cement replacements as nanopozzolan modified cement (NPMC in cement based product by focusing on the evidence of pozzolanic reactivity in corroboration with physical and mechanical properties. Characterization and morphology techniques using X-ray diffraction (XRD, Fourier transform infrared spectroscopy (FTIR, energy-dispersive X-ray spectroscopy (EDS, and scanning electron microscopy (SEM were carried out to assess the pozzolanic reactivity of cement paste modified with the combination of nano- and micro silica as NPMC in comparison to unmodified cement paste (UCP of 0.5 water to cement ratio (w/c. Results were then substantiated with compressive strength (CS results as mechanical property. Results of this study showed clear evidence of pozzolanicity for all samples with varying reactivity with NPMC being the most reactive.

  16. Present and future of glass-ionomers and calcium-silicate cements as bioactive materials in dentistry: Biophotonics-based interfacial analyses in health and disease

    OpenAIRE

    Watson, Timothy F; Atmeh, Amre R.; Sajini, Shara; Cook, Richard J.; Festy, Frederic

    2014-01-01

    Objective Since their introduction, calcium silicate cements have primarily found use as endodontic sealers, due to long setting times. While similar in chemistry, recent variations such as constituent proportions, purities and manufacturing processes mandate a critical understanding of service behavior differences of the new coronal restorative material variants. Of particular relevance to minimally invasive philosophies is the potential for ion supply, from initial hydration to mature set i...

  17. Effect of addition of nano-hydroxyapatite on physico-chemical and antibiofilm properties of calcium silicate cements

    Science.gov (United States)

    GUERREIRO-TANOMARU, Juliane Maria; VÁZQUEZ-GARCÍA, Fernando Antonio; BOSSO-MARTELO, Roberta; BERNARDI, Maria Inês Basso; FARIA, Gisele; TANOMARU, Mario

    2016-01-01

    ABSTRACT Objective Mineral Trioxide Aggregate (MTA) is a calcium silicate cement composed of Portland cement (PC) and bismuth oxide. Hydroxyapatite has been incorporated to enhance mechanical and biological properties of dental materials. This study evaluated physicochemical and mechanical properties and antibiofilm activity of MTA and PC associated with zirconium oxide (ZrO2) and hydroxyapatite nanoparticles (HAn). Material and Methods White MTA (Angelus, Brazil); PC (70%)+ZrO2 (30%); PC (60%)+ZrO2 (30%)+HAn (10%); PC (50%)+ZrO2 (30%)+HAn (20%) were evaluated. The pH was assessed by a digital pH-meter and solubility by mass loss. Setting time was evaluated by using Gilmore needles. Compressive strength was analyzed by mechanical test. Samples were radiographed alongside an aluminum step wedge to evaluate radiopacity. For the antibiofilm evaluation, materials were placed in direct contact with E. faecalis biofilm induced on dentine blocks. The number of colony-forming units (CFU mL-1) in the remaining biolfilm was evaluated. The results were submitted to ANOVA and the Tukey test, with 5% significance. Results There was no difference in pH levels of PC+ZrO2, PC+ZrO2+HAn (10%) and PC+ZrO2+HAn (20%) (p>0.05) and these cements presented higher pH levels than MTA (p<0.05). The highest solubility was observed in PC+ZrO2+HAn (10%) and PC+ZrO2+HAn (20%) (p<0.05). MTA had the shortest initial setting time (p<0.05). All the materials showed radiopacity higher than 3 mmAl. PC+ZrO2 and MTA had the highest compressive strength (p<0.05). Materials did not completely neutralize the bacterial biofilm, but the association with HAn provided greater bacterial reduction than MTA and PC+ZrO2 (p<0.05) after the post-manipulation period of 2 days. Conclusions The addition of HAn to PC associated with ZrO2 harmed the compressive strength and solubility. On the other hand, HAn did not change the pH and the initial setting time, but improved the radiopacity (HAn 10%), the final setting time

  18. Structural study and crystallography of the major compound of anhydrous cement: tri-calcium silicate; Etude structurale et cristallographie du compose majoritaire du ciment anhydre: le silicate tricalcique

    Energy Technology Data Exchange (ETDEWEB)

    Noirfontaine, M.N. de

    2000-01-01

    Anhydrous (Portland) cement is mainly composed of a synthetic material, the clinker, whose major compound is tri-calcium silicate (Ca{sub 3}SiO{sub 5}), often referred as C{sub 3}S with the compact oxides notations, C = CaO et S = SiO{sub 2}. The polymorphism of C{sub 3}S, still not well known, is the main subject of the thesis. Various crystal structures (rhombohedral R, monoclinic M1, M2, M3 and triclinic T1, T2, T3) can be found, depending on temperature and impurities. The only known structures are T1, M1 and M3, involving large unit cells with an orientational disorder of silicate tetrahedra. The single crystal studies exhibit no clear relation between the various polymorphs. Starting from known results from literature single crystal experiments, we establish the metric and structural relations between the different structures. Averaged structures for the T1, M1 and M3 polymorphs are proposed, together with all the matrices of transformation between the unit cells. We also introduce new 1-D, 2-D, and 3-D structural units, which make easier the understanding of the structures of C{sub 3}S, with the result of a better description of the orientational disorder. The effects of impurities on the structure are discussed. In industrial clinkers, impurities stabilize mainly M1 and M3 monoclinic forms. We propose a space group (Pc) and two structural models (a superstructure and an approximate averaged structure) for the M1 form. All the models are validated on synthetic compounds (M3, M2, M1 et T1) and industrial clinkers analysed by X-Ray powder diffraction with Rietveld analysis. (author)

  19. Using calcium silicate to regulate the physicochemical and biological properties when using β-tricalcium phosphate as bone cement

    International Nuclear Information System (INIS)

    β-Tricalcium phosphate (β-TCP) is an osteoconductive material. For this research we have combined it with a low degradation calcium silicate (CS) to enhance its bioactive and osteostimulative properties. To check its effectiveness, a series of β-TCP/CS composites with different ratios were prepared to make new bioactive and biodegradable biocomposites for bone repair. Regarding the formation of bone-like apatite, the diametral tensile strength as well as the ion release and weight loss of composites were compared both before and after immersions in simulated body fluid (SBF). In addition, we also examined the behavior of human dental pulp cells (hDPCs) cultured on β-TCP/CS composites. The results show that the apatite deposition ability of the β-TCP/CS composites improves as the CS content is increased. For composites with more than a 60% CS content, the samples become completely covered by a dense bone-like apatite layer. At the end of the immersion period, weight losses of 24%, 32%, 34%, 38%, 41%, and 45% were observed for the composites containing 0%, 20%, 40%, 80%, 80% and 100% β-TCP cements, respectively. In addition, the antibacterial activity of CS/β-TCP composite improves as the CS-content is increased. In vitro cell experiments show that the CS-rich composites promote human dental pulp cell (hDPC) proliferation and differentiation. However, when the CS quantity in the composite is less than 60%, the quantity of cells and osteogenesis protein of hDPCs is stimulated by Si released from the β-TCP/CS composites. The degradation of β-TCP and the osteogenesis of CS give strong reason to believe that these calcium-based composite cements will prove to be effective bone repair materials. - Highlights: • CS improved the physicochemical properties and osteogenic activity of β-TCP. • Higher CS in the composite, the shorter setting time and the higher DTS was found. • With a CS more than 40%, the osteogenesis and angiogenesis proteins were promoted by

  20. Using calcium silicate to regulate the physicochemical and biological properties when using β-tricalcium phosphate as bone cement

    Energy Technology Data Exchange (ETDEWEB)

    Kao, Chia-Tze; Huang, Tsui-Hsien [School of Dentistry, Chung Shan Medical University, Taichung, Taiwan (China); Department of Dentistry, Chung Shan Medical University Hospital, Taichung, Taiwan (China); Chen, Yi-Jyun [School of Dentistry, Chung Shan Medical University, Taichung, Taiwan (China); Department of Dentistry, Chung Shan Medical University Hospital, Taichung, Taiwan (China); Dental Department, Taichung Hospital, Ministry of Health and Welfare, Taichung City, Taiwan (China); Hung, Chi-Jr [School of Dentistry, Chung Shan Medical University, Taichung, Taiwan (China); Department of Dentistry, Chung Shan Medical University Hospital, Taichung, Taiwan (China); Lin, Chi-Chang, E-mail: chichang31@gmail.com [Department of Chemical and Materials Engineering, Tunghai University, Taichung, Taiwan (China); Shie, Ming-You, E-mail: eviltacasi@gmail.com [Department of Chemical and Materials Engineering, Tunghai University, Taichung, Taiwan (China)

    2014-10-01

    β-Tricalcium phosphate (β-TCP) is an osteoconductive material. For this research we have combined it with a low degradation calcium silicate (CS) to enhance its bioactive and osteostimulative properties. To check its effectiveness, a series of β-TCP/CS composites with different ratios were prepared to make new bioactive and biodegradable biocomposites for bone repair. Regarding the formation of bone-like apatite, the diametral tensile strength as well as the ion release and weight loss of composites were compared both before and after immersions in simulated body fluid (SBF). In addition, we also examined the behavior of human dental pulp cells (hDPCs) cultured on β-TCP/CS composites. The results show that the apatite deposition ability of the β-TCP/CS composites improves as the CS content is increased. For composites with more than a 60% CS content, the samples become completely covered by a dense bone-like apatite layer. At the end of the immersion period, weight losses of 24%, 32%, 34%, 38%, 41%, and 45% were observed for the composites containing 0%, 20%, 40%, 80%, 80% and 100% β-TCP cements, respectively. In addition, the antibacterial activity of CS/β-TCP composite improves as the CS-content is increased. In vitro cell experiments show that the CS-rich composites promote human dental pulp cell (hDPC) proliferation and differentiation. However, when the CS quantity in the composite is less than 60%, the quantity of cells and osteogenesis protein of hDPCs is stimulated by Si released from the β-TCP/CS composites. The degradation of β-TCP and the osteogenesis of CS give strong reason to believe that these calcium-based composite cements will prove to be effective bone repair materials. - Highlights: • CS improved the physicochemical properties and osteogenic activity of β-TCP. • Higher CS in the composite, the shorter setting time and the higher DTS was found. • With a CS more than 40%, the osteogenesis and angiogenesis proteins were promoted by

  1. Calcium and magnesium silicate hydrates

    International Nuclear Information System (INIS)

    Deep geological disposals are planed to discard long-lived intermediate-level and high-level radioactive wastes. Clay-based geological barriers are expected to limit the ingress of groundwater and to reduce the mobility of radioelements. In the interaction zone between the cement and the clay based material alteration can occur. Magnesium silicate hydrates (M-S-H) have been observed due to the reaction of magnesium sulfate containing groundwater with cements or in the interaction zone between low-pH type cement and clays. M-S-H samples synthesized in the laboratory showed that M-S-H has a variable composition within 0.7 ≤ Mg/Si ≤ 1.5. TEM/EDS analyses show an homogeneous gel with no defined structure. IR and 29Si NMR data reveal a higher polymerization degree of the silica network in M-S-H compared to calcium silicate hydrates (C-S-H). The presence of mainly Q3 silicate tetrahedrons in M-S-H indicates a sheet like or a triple-chain silica structure while C-S-H is characterised by single chain-structure. The clear difference in the silica structure and the larger ionic radius of Ca2+ (1.1 Angstrom) compared to Mg2+ (0.8 Angstrom) make the formation of an extended solid solution between M-S-H and C-S-H gel improbable. In fact, the analyses of synthetic samples containing both magnesium and calcium in various ratios indicate the formation of separate M-S-H and C-S-H gels with no or very little uptake of magnesium in CS-H or calcium in M-S-H

  2. Human tooth germ stem cell response to calcium-silicate based endodontic cements

    Directory of Open Access Journals (Sweden)

    Esra Pamukcu Guven

    2013-07-01

    Full Text Available OBJECTIVE: The aim of this study was to compare the cytotoxic effects of endodontic cements on human tooth germ stem cells (hTGSCs. MTA Fillapex, a mineral trioxide aggregate (MTA-based, salicylate resin containing root canal sealer, was compared with iRoot SP, a bioceramic sealer, and AH Plus Jet, an epoxy resin-based root canal sealer. MATERIAL AND METHODS: To evaluate cytotoxicity, all materials were packed into Teflon rings (4 mmµ3 mm and co-cultured with hTGSCs with the aid of 24-well Transwell permeable supports, which had a pore size of 0.4 µm. Coverslips were coated with MTA Fillapex, iRoot SP and AH Plus Jet and each coverslip was placed onto the bottom of one well of a six-well plate for scanning electron microscopy (SEM analysis. Before the cytotoxicity and SEM analysis, all samples were stored at 37ºC and at 95% humidity and 5% CO2 for 24 hours to set. The cellular viability was analyzed using MTS test (3-(4,5-dimethyl-thiazol-2-yl-5-(3-carboxy-methoxy-phenyl-2-(4-sulfo-phenyl-2H-tetrazolium. The cytotoxic effects and SEM visualization of the tested materials were analyzed at 24-hour, 72-hour, one-week and two-week periods. RESULTS: On the 1st day, only MTA Fillapex caused cytotoxicity compared to negative control (NC group (p0.05. After 14 days of incubation with the test materials, MTA Fillapex exhibited significantly higher cytotoxicity compared with iRoot SP, AH Plus Jet and the NC group (P<0.008. In the SEM analysis, the highest levels of cell attachment were observed for iRoot SP and the control group. After 24 hours, MTA Fillapex reduced the number of cells attached to the surface. CONCLUSIONS: Within the limitations of this study, sealers exerted different cytotoxic effects on hTGSCs. Although all materials have exerted cellular toxicity, iRoot SP and AH Plus Jet may promote better attachment to hTGSCs.

  3. ToF-SIMS images and spectra of biomimetic calcium silicate-based cements after storage in solutions simulating the effects of human biological fluids

    Science.gov (United States)

    Torrisi, A.; Torrisi, V.; Tuccitto, N.; Gandolfi, M. G.; Prati, C.; Licciardello, A.

    2010-01-01

    ToF-SIMS images were obtained from a section of a tooth, obturated by means of a new calcium-silicate based cement (wTCF) after storage for 1 month in a saline solutions (DPBS), in order to simulate the body fluid effects on the obturation. Afterwards, ToF-SIMS spectra were obtained from model samples, prepared by using the same cement paste, after storage for 1 month and 8 months in two different saline solutions (DPBS and HBSS). ToF-SIMS spectra were also obtained from fluorine-free cement (wTC) samples after storage in HBSS for 1 month and 8 months and used for comparison. It was found that the composition of both the saline solution and the cement influenced the composition of the surface of disks and that longer is the storage greater are the differences. Segregation phenomena occur both on the cement obturation of the tooth and on the surface of the disks prepared by using the same cement. Indirect evidences of formation of new crystalline phases are supplied.

  4. Effects of two fast-setting calcium-silicate cements on cell viability and angiogenic factor release in human pulp-derived cells.

    Science.gov (United States)

    Chung, Chooryung J; Kim, Euiseong; Song, Minju; Park, Jeong-Won; Shin, Su-Jung

    2016-05-01

    Mineral trioxide aggregate (MTA) is considered a pulp-capping agent of choice, but has the drawback of a long setting time. This study aimed to assess two different types of calcium-silicate cements as pulp-capping agents, by investigating their in vitro cytotoxicity and angiogenic effects in human pulp cells. ProRoot MTA, Endocem Zr, and Retro MTA were prepared as set or freshly mixed pellets. Human pulp-derived cells were grown in direct contact with these three cements, Dycal, or no cement, for 7 days. Initial cell attachment, viability, calcium release, and the levels of vascular endothelial growth factor (VEGF), angiogenin, and basic fibroblast growth factor (FGF-2) were evaluated statistically using a linear mixed model (P calcium concentration compared with the control group (P  0.05). We demonstrate that Retro MTA, which has a short setting time, has similar biocompatibility and angiogenic effects on human pulp cells, and can therefore potentially be as effective in pulp capping as ProRoot MTA. Endocem Zr showed intermittent cytotoxicity and elicited lower levels of VEGF and angiogenin expression. PMID:25596932

  5. 21 CFR 573.260 - Calcium silicate.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Calcium silicate. 573.260 Section 573.260 Food and... Listing § 573.260 Calcium silicate. Calcium silicate, including synthetic calcium silicate, may be safely used as an anticaking agent in animal feed, provided that the amount of calcium silicate does...

  6. Aggregation of Calcium Silicate Hydrate Nanoplatelets.

    Science.gov (United States)

    Delhorme, Maxime; Labbez, Christophe; Turesson, Martin; Lesniewska, Eric; Woodward, Cliff E; Jönsson, Bo

    2016-03-01

    We study the aggregation of calcium silicate hydrate nanoplatelets on a surface by means of Monte Carlo and molecular dynamics simulations at thermodynamic equilibrium. Calcium silicate hydrate (C-S-H) is the main component formed in cement and is responsible for the strength of the material. The hydrate is formed in early cement paste and grows to form platelets on the nanoscale, which aggregate either on dissolving cement particles or on auxiliary particles. The general result is that the experimentally observed variations in these dynamic processes generically called growth can be rationalized from interaction free energies, that is, from pure thermodynamic arguments. We further show that the surface charge density of the particles determines the aggregate structures formed by C-S-H and thus their growth modes. PMID:26859614

  7. NMR study of hydrated calcium silicates

    International Nuclear Information System (INIS)

    Radioactive wastes storage methods are developed by the CEA. As cements are important materials as well for hours living radioisotopes than for years living radioisotopes, a better knowledge of this material will allow to anticipate its behaviour and to obtain safer storage methods. The structure of calcium silicates (C-S-H) (main constituent of cements) have then been determined in this thesis by nuclear magnetic resonance. This method has allow to explain in structural terms, the different calcium rates that can be measured in the C-S-H too. (O.M.)

  8. Mechanistic study and modeling of radionuclides retention by the hydrated calcium silicates (HCS) of cements; Etude mecanistique et modelisation de la retention de radionucleides par les silicates de calcium hydrates (CSH) des ciments

    Energy Technology Data Exchange (ETDEWEB)

    Pointeau, I

    2000-09-01

    This work attempts to investigate the modelling of radioisotopes (Cs{sup +}, Pb{sup 2+}, Eu{sup 3+}) immobilization in cement matrix, in the frame of the design of engineered barrier of a deep radwaste repository. The model development concept consists of three major steps: - surface chemistry modelling of the calcium silicate hydrate CSH, used to simulate hydrated cement behaviour; - solid analysis of the batch sorption experiments: identification of the uptake mechanism; - both previous steps are used, with isotherm data, in the modelling of the radioisotopes immobilization in the CSH matrix. Final results: (all modelling are available for all the range of studied Ca/Si ratios and have been validated with predictive calculations). - A thermodynamic modelling of the CSH surface chemistry has been developed. The labile calcium and proton sorption constants on silanol sites (>SiOH) have been extracted. - Cs{sup +} is sorbed on two sites. The silanol site (weak site) has a high site density (10 sites.nm{sup -2}), which accounts for the CSH unsaturation in high [CS{sup +}]. A strong site is also identified. - Pb{sup 2+} immobilization in CSH matrix is modelled with surface equilibria and solubility equilibrium. - Eu{sup 3+} fixation has been investigated with solid analysis: Site-Selective anti Time-Resolved Luminescence Spectroscopy, XPS and SEM-EDS. Eu{sup 3+} thus does not precipitate in CSH water but is sorbed on the CSH surface (high hydroxylated environment). Europium is also (minority site) inserted in the CSH framework. (author)

  9. Chemical alteration of cement materials in a radioactive waste repository environment. 3. Development of reactive transport computational code combined with incongruent dissolution model of calcium silicate hydrates

    International Nuclear Information System (INIS)

    For long-term performance assessment of a cementitious disposal system for TRU waste, a so-called reactive transport computational code, being a numerical simulation code coupled a geochemical model suited to the system includes cement hydrate and a solute transport model, so-called reactive transport computational code, has been developed. The thermodynamic model previously developed in our institute for incongruent dissolution of calcium silicate hydrate (C-S-H) gel, which is a principal product of hydrated cement phase, was incorporated into a geochemical code, Harphrq, to evaluate chemical equilibrium conditions containing cement hydrates. This modification of the code enables a user to evaluate adequately the chemical equilibrium of a system including cement hydrate, such as a dissolution/precipitation of C-S-H gel and/or a change of Ca/Si ratio in C-S-H gel. The modified geochemical code was coupled onto a simplified solute transport code using a compartment model. The coupled code could simulate the processes where various chemical species in aqueous phase migrate through the homogeneous porous materials while locally maintaining chemical equilibrium. The developed reactive transport computational code was verified by comparison with experimental results on batch-type dissolution tests and column-type alteration tests under flow-through conditions of ordinary Portland cement hydrate. Predictive calculation results by the developed code were reasonably accordant with the experimental results, e.g. the distribution of constituent minerals and the composition of pore water in altered ordinary Portland cement hydrate. The validity of the developed code was therefore verified. Analysis on the results by the calculation could indicates special features such as a distribution of Ca/Si ratio in C-S-H gel along the water-flow in the column, and a re-precipitation of C-S-H gel in the downstream side of the dissolution front of C-S-H gel. (author)

  10. In vitro bioactivity of a tricalcium silicate cement

    International Nuclear Information System (INIS)

    Tricalcium silicate is the major constituent of Portland cement and the responsible for their mechanical strength at early stages. In order to be used as and additive of conventional calcium phosphate cement (CPC), in vitro bioactivity of a calcium silicate cement (CSC) after soaking in simulated body fluid (SBF) for 14 days was study. The cement was obtained by mixing Ca3SiO5, obtained by sol-gel process, and a Na2HPO4 solution. The morphological and structural changes of the material before and after soaking were analyzed by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The results showed the formation of a layer of a Hydroxyapatite (HA) onto the CSC cement after soaking for 1h in SBF that became denser with the increase of soaking time. The study suggests that Ca3SiO5 would be an effective additive to improve the bioactivity and long term strength of conventional CPC. (author)

  11. The synergistic effects of CO2 laser treatment with calcium silicate cement of antibacterial, osteogenesis and cementogenesis efficacy

    Science.gov (United States)

    Hsu, T.-T.; Kao, C.-T.; Chen, Y.-W.; Huang, T.-H.; Yang, J.-J.; Shie, M.-Y.

    2015-05-01

    Calcium silicate-based material (CS) has been successfully used in dental clinical applications. Some researches show that the antibacterial effects of CO2 laser irradiation are highly efficient when bacteria are embedded in biofilm, due to a photo-thermal mechanism. The purpose of this study was to confirm the effects of CO2 laser irradiation on CS, with regard to both material characterization and human periodontal ligament cell (hPDLs) viability. CS was irradiated with a dental CO2 laser using directly mounted fiber optics in wound healing mode with a spot area of 0.25 cm2, and then stored in an incubator at 100% relative humidity and 37 °C for 1 d to set. The hPDLs cultured on CS were analyzed, along with their proliferation and odontogenic differentiation behaviors. The results indicate that the CO2 laser irradiation increased the amount of Ca and Si ions released from the CS, and regulated cell behavior. CO2 laser-irradiated CS promoted cementogenic differentiation of hPDLs, with the increased formation of mineralized nodules on the substrate’s surface. It also up-regulated the protein expression of multiple markers of cementogenic and the expression of cementum attachment protein. The current study provides new and important data about the effects of CO2 laser irradiation on CS. Taking cell functions into account, the Si concentration released from CS with laser irradiated may be lower than a critical value, and this information could lead to the development of new regenerative therapies for dentin and periodontal tissue.

  12. Hardening of calcium hydroxide and calcium silicate binders due to carbonation and hydration

    OpenAIRE

    Cizer, Özlem; Campforts, J; Balen, Koenraad Van; Elsen, Jan; Gemert, Dionys van

    2006-01-01

    Hardening of calcium hydroxide and calcium silicate binders composed of cement, rice husk ash (RHA) and lime in different compositions were studied with mechanical strength, mercury intrusion porosimetry, thermal analysis and SEM. When cement is partially replaced with RHA and lime, hardening occurs as a result of combined hydration, pozzolanic reaction and carbonation reaction. While hydration of cement contributes to the early strength development of the mortars, carbonation is much more pr...

  13. Regulation of physicochemical properties, osteogenesis activity, and fibroblast growth factor-2 release ability of β-tricalcium phosphate for bone cement by calcium silicate

    Energy Technology Data Exchange (ETDEWEB)

    Su, Ching-Chuan [Antai Medical Care Cooperation Antai Tian-Sheng Memorial Hospital, Pingtung, Taiwan (China); Kao, Chia-Tze; Hung, Chi-Jr [School of Dentistry, Chung Shan Medical University, Taichung, Taiwan (China); Department of Dentistry, Chung Shan Medical University Hospital, Taichung, Taiwan (China); Chen, Yi-Jyun [School of Dentistry, Chung Shan Medical University, Taichung, Taiwan (China); Department of Dentistry, Chung Shan Medical University Hospital, Taichung, Taiwan (China); Dental Department, Taichung Hospital, Ministry of Health and Welfare, Taichung City, Taiwan (China); Huang, Tsui-Hsien, E-mail: thh@csmu.edu.tw [School of Dentistry, Chung Shan Medical University, Taichung, Taiwan (China); Department of Dentistry, Chung Shan Medical University Hospital, Taichung, Taiwan (China); Shie, Ming-You, E-mail: eviltacasi@gmail.com [Institute of Oral Science, Chung Shan Medical University, Taichung, Taiwan (China)

    2014-04-01

    β-Tricalcium phosphate (β-TCP) is an osteoconductive material. For this research we have combined it with a low degradation calcium silicate (CS) to enhance its bioactive and osteostimulative properties. To check its effectiveness, a series of β-TCP/CS composites with different ratios were prepared to make new bioactive and biodegradable biocomposites for bone repair. Formation of bone-like apatite, the diametral tensile strength, and weight loss of composites were considered before and after immersion in simulated body fluid (SBF). In addition, we also examined the effects of fibroblast growth factor-2 (FGF-2) released from β-TCP/CS composites and in vitro human dental pulp cell (hDPC) and studied its behavior. The results showed that the apatite deposition ability of the β-TCP/CS composites was enhanced as the CS content was increased. For composites with more than 50% CS contents, the samples were completely covered by a dense bone-like apatite layer. At the end of the immersion point, weight losses of 19%, 24%, 33%, 42%, and 51% were observed for the composites containing 0%, 30%, 50%, 70% and 100% β-TCP cements, respectively. In vitro cell experiments show that the CS-rich composites promote human dental pulp cell (hDPC) proliferation and differentiation. However, when the CS quantity in the composite is less than 70%, the amount of cells and osteogenesis protein of hDPCs was stimulated by FGF-2 released from β-TCP/CS composites. The combination of FGF-2 in degradation of β-TCP and osteogenesis of CS gives a strong reason to believe that these calcium-based composite cements may prove to be promising bone repair materials. - Highlights: • CS improved physicochemical properties and osteogenic activity of β-TCP. • The higher the CS in the cement, the shorter the setting time and the higher the DTS. • The cell behavior was stimulated by FGF-2 released from composite containing 50% CS. • β-TCP/CS composite with FGF-2 has optimal properties for

  14. Regulation of physicochemical properties, osteogenesis activity, and fibroblast growth factor-2 release ability of β-tricalcium phosphate for bone cement by calcium silicate

    International Nuclear Information System (INIS)

    β-Tricalcium phosphate (β-TCP) is an osteoconductive material. For this research we have combined it with a low degradation calcium silicate (CS) to enhance its bioactive and osteostimulative properties. To check its effectiveness, a series of β-TCP/CS composites with different ratios were prepared to make new bioactive and biodegradable biocomposites for bone repair. Formation of bone-like apatite, the diametral tensile strength, and weight loss of composites were considered before and after immersion in simulated body fluid (SBF). In addition, we also examined the effects of fibroblast growth factor-2 (FGF-2) released from β-TCP/CS composites and in vitro human dental pulp cell (hDPC) and studied its behavior. The results showed that the apatite deposition ability of the β-TCP/CS composites was enhanced as the CS content was increased. For composites with more than 50% CS contents, the samples were completely covered by a dense bone-like apatite layer. At the end of the immersion point, weight losses of 19%, 24%, 33%, 42%, and 51% were observed for the composites containing 0%, 30%, 50%, 70% and 100% β-TCP cements, respectively. In vitro cell experiments show that the CS-rich composites promote human dental pulp cell (hDPC) proliferation and differentiation. However, when the CS quantity in the composite is less than 70%, the amount of cells and osteogenesis protein of hDPCs was stimulated by FGF-2 released from β-TCP/CS composites. The combination of FGF-2 in degradation of β-TCP and osteogenesis of CS gives a strong reason to believe that these calcium-based composite cements may prove to be promising bone repair materials. - Highlights: • CS improved physicochemical properties and osteogenic activity of β-TCP. • The higher the CS in the cement, the shorter the setting time and the higher the DTS. • The cell behavior was stimulated by FGF-2 released from composite containing 50% CS. • β-TCP/CS composite with FGF-2 has optimal properties for

  15. 21 CFR 182.2227 - Calcium silicate.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Calcium silicate. 182.2227 Section 182.2227 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) SUBSTANCES GENERALLY RECOGNIZED AS SAFE Anticaking Agents § 182.2227 Calcium silicate. (a) Product. Calcium silicate....

  16. 21 CFR 582.2227 - Calcium silicate.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Calcium silicate. 582.2227 Section 582.2227 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Calcium silicate. (a) Product. Calcium silicate. (b) Tolerance. 2 percent and 5 percent. (c)...

  17. Chemical alteration of cement materials in a radioactive waste repository environment. 1. Thermodynamic modelling for the dissolution and precipitation of calcium silicate hydrates

    International Nuclear Information System (INIS)

    Cementitious material, a potential waste packaging and backfilling material for the disposal of radioactive waste, is expected to provide both physical and chemical containment. In particular the ability to provide high-pH conditions, which depends on the solubility of the constituent hydrated minerals in cement matrices, is a very important parameter when considering the release of radionuclides from radio active wastes. For long-term safety assessment, it is necessary to develop a series of predictive calculation models. Several models have been proposed for the incongruent dissolution of calcium silicate hydrate (C-S-H) gel, which is the principal product of hydrated cement phases. In the repository, the re-precipitation of minerals would follow their dissolution when an equilibrated solution moves to the other regions and equilibrates with the constituent minerals there. However, previous models have not yet adequately quantitatively evaluated the re-precipitation or interaction of other minerals with the dissolution of C-S-H gel. In this study, therefore, a thermodynamic dissolution and precipitation model of C-S-H gel is proposed assuming a binary non-ideal solid solution of Ca(OH)2 and Si02. Dissolution and precipitation experiments on C-S-H gel were performed. C-S-H precipitates were prepared using two techniques. One was based on hydrolysis in a mixture of Ca and Si solutions and produced homogeneous gels. With the other technique, precipitates were prepared by contacting Ca(OH)2 solution with C-S-H gel with low Ca/Si ratios (0.47, 0.65, 0.9). The results were well predicted by the proposed model. Dissolution experiments on C-S-H gel coexisting with ettringite were also carried out. At Ca/Si>l.2 in C-S-H gel, the equilibrated pH and Ca and Si concentrations are nearly the same as those for C-S-H gel alone. At lower Ca/Si, interaction between ettringite and C-S-H dissolution was observed more clearly. The measured pH and Ca and Si concentrations were

  18. Dealkalization of calcium silicate slag and study of using it as cement admixture%硅钙渣脱碱处理及作水泥混合材的研究

    Institute of Scientific and Technical Information of China (English)

    刘江; 张建波; 孙俊民; 王宏霞; 叶家元; 史迪

    2012-01-01

    Orthogonal experiment method is applied to research on dealkalization of calcium silicate slag, and properties of non-dealkalizated and dealkalizated calcium slag cement have been analyzed. Effects of temperature, holding time, content of lime milk and washing times were discussed, the results show that the optimum dealkalization combination of the four factors is as follows:content of lime milk is 10%,temperature 85 X. and holding time 3 hours,washing twice,then an alkali content of 0.83% will be acquired; compressive strength of non梔ealkalizated calcium slag cement is higher than dealkalizated calcium slag cement during the early hydration, the advantages of dealkalizated calcium slag cement will gradually appear as time goes and will be more significantly as calcium slag content increase; Microscopic analysis shows that non-dealkalizated calcium slag cement generates large amount of C-S-H gel during early hydration and its hydration products are more compact than dealkalizated calcium slag cement, little difference of the compactness has been found between them when the hydration time is 28 days.%采用正交试验法对硅钙渣进行脱碱处理,对脱碱前后的硅钙渣水泥性能进行了研究.通过调整温度、保温时间、石灰乳掺量和水洗次数,得出最佳脱碱组合为:石灰乳掺量10%,温度85℃,保温时间3h,水洗2次,处理后碱含量为0.83%:强度试验结果表明,水化早期未脱碱硅钙渣水泥抗压强度要高于脱碱硅钙渣水泥,但随着龄期逐渐增长,脱碱硅钙渣水泥优势逐渐显现,掺量越大优势越明显;微观形貌分析表明,未脱碱硅钙渣水泥水化早期生成大量C-S-H凝胶,水化产物较脱碱硅钙渣水泥更致密,水化28d时两者水化产物的致密性相当.

  19. Quantitative Evaluation by Glucose Diffusion of Microleakage in Aged Calcium Silicate-Based Open-Sandwich Restorations

    OpenAIRE

    Camps, J.; Tassery, H.; Koubi, G.; Elmerini, H.; Koubi, S.

    2012-01-01

    This study compared the in vitro marginal integrity of open-sandwich restorations based on aged calcium silicate cement versus resin-modified glass ionomer cement. Class II cavities were prepared on 30 extracted human third molars. These teeth were randomly assigned to two groups ( = 1 0 ) to compare a new hydraulic calcium silicate cement designed for restorative dentistry (Biodentine, Septodont, Saint Maur des Fossés, France) with a resin-modified glass ionomer cement (Ionolux, Voco, Cuxh...

  20. Sealing of cracks in cement using microencapsulated sodium silicate

    Science.gov (United States)

    Giannaros, P.; Kanellopoulos, A.; Al-Tabbaa, A.

    2016-08-01

    Cement-based materials possess an inherent autogenous self-healing capability allowing them to seal, and potentially heal, microcracks. This can be improved through the addition of microencapsulated healing agents for autonomic self-healing. The fundamental principle of this self-healing mechanism is that when cracks propagate in the cementitious matrix, they rupture the dispersed capsules and their content (cargo material) is released into the crack volume. Various healing agents have been explored in the literature for their efficacy to recover mechanical and durability properties in cementitious materials. In these materials, the healing agents are most commonly encapsulated in macrocontainers (e.g. glass tubes or capsules) and placed into the material. In this work, microencapsulated sodium silicate in both liquid and solid form was added to cement specimens. Sodium silicate reacts with the calcium hydroxide in hydrated cement paste to form calcium-silicate-hydrate gel that fills cracks. The effect of microcapsule addition on rheological and mechanical properties of cement is reported. It is observed that the microcapsule addition inhibits compressive strength development in cement and this is observed through a plateau in strength between 28 and 56 days. The improvement in crack-sealing for microcapsule-containing specimens is quantified through sorptivity measurements over a 28 day healing period. After just seven days, the addition of 4% microcapsules resulted in a reduction in sorptivity of up to 45% when compared to specimens without any microcapsule addition. A qualitative description of the reaction between the cargo material and the cementitious matrix is also provided using x-ray diffraction analysis.

  1. Calcium Aluminate Cement Hydration Model

    Directory of Open Access Journals (Sweden)

    Matusinović, T.

    2011-01-01

    Full Text Available Calcium aluminate cement (AC is a very versatile special cement used for specific applications. As the hydration of AC is highly temperature dependent, yielding structurally different hydration products that continuously alter material properties, a good knowledge of thermal properties at early stages of hydration is essential. The kinetics of AC hydration is a complex process and the use of single mechanisms models cannot describe the rate of hydration during the whole stage.This paper examines the influence of temperature (ϑ=5–20 °C and water-to-cement mass ratio (mH /mAC = 0.4; 0.5 and 1.0 on hydration of commercial iron-rich AC ISTRA 40 (producer: Istra Cement, Pula, Croatia, which is a part of CALUCEM group, Figs 1–3. The flow rate of heat generation of cement pastes as a result of the hydration reactions was measured with differential microcalorimeter. Chemically bonded water in the hydrated cement samples was determined by thermo-gravimetry.Far less heat is liberated when cement and water come in contact for the first time, Fig. 1, than in the case for portland cement (PC. Higher water-to-cement ratio increases the heat evolved at later ages (Fig. 3 due to higher quantity of water available for hydration. A significant effect of the water-to-cement ratio on the hydration rate and hydration degree showed the importance of water as being the limiting reactant that slows down the reaction early. A simplified stoichiometric model of early age AC hydration (eq. (8 based on reaction schemes of principal minerals, nominally CA, C12A7 and C4AF (Table 1, was employed. Hydration kinetics after the induction period (ϑ < 20 °C had been successfully described (Fig. 4 and Table 2 by a proposed model (eq. (23 which simultaneously comprised three main mechanisms: nucleation and growth, interaction at phase boundary, and mass transfer. In the proposed kinetic model the nucleation and growth is proportional to the amount of reacted minerals (eq

  2. Interaction of calcium silicate hydrates (C-S-H), the main components of cement, with alkaline chlorides, analogy with clays; Interaction des silicates de calcium hydrates, principaux constituants du ciment, avec les chlorures d'alcalins. Analogie avec les argiles

    Energy Technology Data Exchange (ETDEWEB)

    Viallis-Terrisse, H

    2000-10-06

    This work, belonging to a more general study on the structure and reactivity of cement, deals with the experimental and theoretical analysis of the interaction of alkaline chlorides with calcium silicate hydrates (C-S-H), the main components of cement paste. The interaction of alkaline cations with C-S-H is interfacial, involving both electrostatic and surface complexation mechanisms. The C-S-H surface is constituted of silanol sites, partially dissociated due to the high pH of the interstitial solution. The calcium ions, present in large amounts in the equilibrium solution of C-S-H, constitute potential determining ions for the C-S-H surface. The alkaline ions seem to compete with calcium for the same surface sites. The adsorption isotherms show that caesium presents a better affinity than sodium and lithium for the C-S-H surface. Moreover, solid-state NMR suggests that caesium forms with the surface sites inner-sphere complexes, whereas sodium seems to keep its hydration sphere. These results are in agreement with zeta potential measurements, which let suppose a specific adsorption of caesium ions, and an indifferent behaviour of both other alkaline ions. A model for the C-S-H surface was proposed, from the electric double layer model, and mass action laws expressing the complexation of the different ionic species with the silanol sites. The whole study relies on a structural analogy with smectites, some clays presenting well-known cationic adsorption properties. The structural similarity between both minerals is enhanced by some similarities of reactivity, though significant behaviour differences could also be noted. (author)

  3. 21 CFR 172.410 - Calcium silicate.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Calcium silicate. 172.410 Section 172.410 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION Anticaking Agents § 172.410 Calcium...

  4. Solubility of a new calcium silicate-based root-end filling material

    OpenAIRE

    Shishir Singh; Rajesh Podar; Shifali Dadu; Gaurav Kulkarni; Rucheet Purba

    2015-01-01

    Introduction: The purpose of this study was to compare solubility of a new calcium silicate-based cement, Biodentine with three commonly used root-end filling materials viz. glass-ionomer cement (GIC), intermediate restorative material (IRM), and mineral trioxide aggregate (MTA). Materials and Methods: Twenty stainless steel ring molds were filled with cements corresponding to four groups (n = 5). The weight of 20 dried glass bottles was recorded. Samples were transferred to bottles conta...

  5. Thermogravimetric analysis of phase transitions in cement compositions mixed by sodium silicate solution

    Directory of Open Access Journals (Sweden)

    Fedosov Sergey Viktorovich

    2014-01-01

    Full Text Available This paper presents a study of the capability to modify cement by mechanical activation of sodium silicate water solution. Admixtures or blends of binding agents were employed for modifying concrete properties. The liquid glass is applied to protect from chemically or physically unfavorable environmental impacts, such as acidic medium and high temperature. The sodium silicate is a high-capacity setting accelerator. The increasing of the liquid glass proportion in the mix leads to the degradation of the cement paste plasticity and for this reason it is necessary to reduce the amount of liquid glass in the cement paste. The activation of dilute water solution of sodium silicate into rotary pulsating apparatus directly before tempering of the cement paste is an effective way to decrease mass fraction of liquid glass in the cement paste. The results of the combined influence of liquid glass and mechanical activation on physicochemical processes taking place in cement stone are represented in this research. Thermogravimetric analysis was used in order to study cement blends. Thermogravimetric analysis of modified cement stone assays was performed by thermo analyzer SETARAM TGA 92-24. The results of the analysis of phase transition taking place under high-temperature heating of cement stone modified by the mechanical activation of the water solution of the sodium silicate were introduced. Thermograms of cement stone assays were obtained at different hardening age. The comparison of these thermograms allows us to come to a conclusion on the formation and the retention during long time of a more dense structure of the composite matrix mixed by the mechanical activation of sodium silicate water solution. The relation between the concrete composition and its strength properties was stated. Perhaps, the capability of modified concrete to keep calcium ions in sparingly soluble hydrosilicates leads to the increase in its durability and corrosion resistance.

  6. 21 CFR 182.2122 - Aluminum calcium silicate.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Aluminum calcium silicate. 182.2122 Section 182.2122 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED....2122 Aluminum calcium silicate. (a) Product. Aluminum calcium silicate. (b) Tolerance. 2 percent....

  7. 21 CFR 582.2122 - Aluminum calcium silicate.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Aluminum calcium silicate. 582.2122 Section 582.2122 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED....2122 Aluminum calcium silicate. (a) Product. Aluminum calcium silicate. (b) Tolerance. 2 percent....

  8. Study on silicate-calcium phosphate composite bone cement modified by sodium carbonate solution%碳酸钠液相改性硅-磷酸钙复合骨水泥研究

    Institute of Scientific and Technical Information of China (English)

    李青林; 杨帮成

    2014-01-01

    以质量分数70%的硅酸三钙(Ca3 SiO5,C3 S)和30%磷酸氢钙(CaHPO4·2H2 O,DCPD)复合得到的 DCP30粉体材料为固相,以不同浓度碳酸钠溶液为液相,得到碳酸钠改性骨水泥材料。使用 X 射线衍射(XRD)、扫描电镜(SEM)、万能材料试验机等手段对不同浓度改性材料进行表征。结果显示:添加碳酸钠液相,骨水泥初、终凝时间分别缩短至16和55 min;调控碳酸钠液相浓度,可以实现短期抗压强度优化;使用碳酸钠后,固化自发生成羟基磷灰石(HA)。浸泡模拟体液(SBF)7天,材料表面覆盖 HA 沉积层,生物活性优越。碳酸钠液相改性硅-磷酸钙复合骨水泥体系的水化性能、短期力学性能以及生物活性均优于Ca3 SiO5水泥和未改性硅-磷酸钙复合骨水泥,是一种良好的生物活性骨修复材料。%Sodium carbonate solution modified bone cement materials have been prepared using sodium carbonate solution with dif-ferent concentration as liquid phase and DCP30 powder material obtained by 70% mass fraction tricalcium silicate (Ca3 SiO5 ,C3 S) and 30% dicalcium phosphate (CaHPO4 ·2H2 O,DCPD)as the solid phase.The materials were characterized by the means of X-ray diffraction (XRD),scanning electron microscope (SEM)and mechanical test.The results show that the initial and final set-ting time of bone cement is reduced to 16 and 55 min by the addition of sodium carbonate solution.The short-term mechanical strength can be optimized by controlling the concentration of sodium carbonate solution.Hydroxyapatite (HA)can spontaneously form after the use of sodium carbonate solution.HA forms on the surface of bone-cement after immersion in SBF for 7 days,indi-cating its good bioactivity.The modified system shows better hydraulic property,bioactivity and mechanical strength than Ca3 SiO5 cement and unmodifiled silicate-calcium phosphate composite bone cement,suggesting the new system is a

  9. CO2 sequestration using calcium-silicate concrete

    International Nuclear Information System (INIS)

    This study examined the feasibility of sequestering carbon dioxide (CO2) using calcium silicate while developing a strong and durable concrete building product. In addition to offering a solution for a safe, environmentally sound manner to sequester carbon dioxide, the carbonation curing of concrete has the potential to provide a permanent storage for exhaust CO2. The calcium compounds in cement react with CO2 through the early-age carbonation curing, forming geologically stable calcium carbonates. In this study, both type 10 and type 30 Portland cements were used as CO2 binders in concretes with 0, 25, 50, and 75 per cent quartz aggregates and lightweight aggregates. The sequestration took place in a chamber under 0.5 MPa pressure at ambient temperature for a duration of 2 hours. The recovered CO2 from flue gas was simulated using a 100 per cent concentration of CO2. The CO2 uptake was quantified by direct mass gain and by an infrared-based carbon analyzer. The performance of the carbonated concrete was evaluated by its strength. In 2 hours, a CO2 uptake of 9 to 16 per cent by binder mass was achieved. The carbonation curing of concrete was found to provide better strength, stability, permeability and abrasion resistance in concrete products without steel reinforcement. 10 refs., 4 tabs., 10 figs

  10. (α'(H))-Dicalcium silicate bone cement doped with tricalcium phosphate: characterization, bioactivity and biocompatibility.

    Science.gov (United States)

    de Aza, Piedad N; Zuleta, Fausto; Velasquez, Pablo; Vicente-Salar, Nestor; Reig, Juan A

    2014-02-01

    The influence of phosphorus doping on the properties of (α'(H))-dicalcium silicate (C(2)S) bone cement was analyzed, in addition to bioactivity and biocompatibility. All the cements were composed of a solid solution of TCP in C(2)S ([Formula: see text]-C(2)S(ss)) as the only phase present. The compressive strength ranged from 3.8-16.3 MPa. Final setting times ranged from 10 to 50 min and were lower for cements with lower L/P content. Calcium silicate hydrate was the principal phase formed during the hydration process of the cements. The cement exhibited a moderate degradation and could induce carbonated hydroxyapatite formation on its surface and into the pores. The cell attachment test showed that the (α'(H))-C(2)SiO(4) solid solution supported human adipose stem cells adhesion and spreading, and the cells established close contacts with the cement after 24 h of culture. The novel (α'(H))-C(2)S(ss) cements might be suitable for potential applications in the biomedical field, preferentially as materials for bone/dental repair. PMID:24218299

  11. Evaluation of long-term interaction between cement and bentonite for geological disposal (2) XAFS analysis of calcium silicate hydrate precipitates at cementitious and bentonite material interface

    International Nuclear Information System (INIS)

    Document available in extended abstract form only. Numerical analyses of the long-term alteration of the engineered barriers used for the disposal of TRU waste predicted precipitation of C-S-H minerals at the interface between the cementitious materials and the bentonite-based buffer. When the C-S-H precipitates at this interface, the diffusion coefficient in the engineered barriers will decrease, resulting in reduced mass transport, which feeds back to reduce the rate of subsequent alteration. The C-S-H predicted to form at the cement-bentonite interface could not be identified directly using conventional analytical tools, including XRD, due to its low crystallinity. The authors propose that XAFS analysis, which provides spectra sensitive to the valency and coordination of the element of interest regardless of its crystallinity, would be capable of characterizing the C-S-H. The presence of the C-S-H precipitated as a secondary mineral has already been confirmed by applying chemical and XAFS analyses to bentonite specimens collected from the compacted bentonite-cement interface. However, because of the limitations on the width of specimens that can be collected by cutting from block samples, i.e. approximately 1 mm, detailed concentration profiles could not be obtained for this secondary C-S-H. In this study, XAFS spectra of thin specimens were measured using an X-ray detector in order to obtain detailed concentration profiles for the C-S-H formed at the interface between the cementitious material and the bentonite-based buffer. The X-ray detector used in the XAFS analysis consists of 1024 photodiodes arranged in line with a 0.025 mm pitch (photodiode array; PDA). Ca-K-edge XAFS measurements were conducted at the Photon Factory of the KEK. The synchrotron was operated in top-up mode with 450 mA during the measurements. Specimens were taken from a contact sample of compacted bentonite (Kunigel V1; dry density of 1.6 g/cm3) and hardened OPC (w/c = 0.6) immersed in

  12. Properties of Chemically Combusted Calcium Carbide Residue and Its Influence on Cement Properties

    OpenAIRE

    Hongfang Sun; Zishanshan Li; Jing Bai; Shazim Ali Memon; Biqin Dong; Yuan Fang; Weiting Xu; Feng Xing

    2015-01-01

    Calcium carbide residue (CCR) is a waste by-product from acetylene gas production. The main component of CCR is Ca(OH)2, which can react with siliceous materials through pozzolanic reactions, resulting in a product similar to those obtained from the cement hydration process. Thus, it is possible to use CCR as a substitute for Portland cement in concrete. In this research, we synthesized CCR and silica fume through a chemical combustion technique to produce a new reactive cementitious powder (...

  13. Calcium phosphate cements properties with polymers addition

    International Nuclear Information System (INIS)

    Calcium phosphate cements (CPC) have attracted great interest to use in orthopedics and dentistry as replacements for damaged parts of the skeletal system, showing good biocompatibility and osseointegration, allowing its use as bone graft. Several studies have shown that the addition of polymer additives have a strong influence on the cement properties. The low mechanical strength is the main obstacle to greater use of CPC as an implant material. The objective of this study was to evaluate properties of a cement based on α-tricalcium phosphate (α-TCP), added polymers. PVA (10%, 8%, 6%), sodium alginate (2%) and polyacrylate ammonia (3%), all in weight, were added to the synthesized α-TCP powder. The samples were molded and evaluated for density, porosity in vitro test (Simulated Body Fluid), crystalline phases and mechanical strength. The results show increased the mechanical properties of the cement when added these polymers

  14. Effects of a discoloration-resistant calcium aluminosilicate cement on the viability and proliferation of undifferentiated human dental pulp stem cells

    OpenAIRE

    Li-na Niu; Devon Watson; Kyle Thames; Carolyn M. Primus; Bergeron, Brian E.; Kai Jiao; Bortoluzzi, Eduardo A.; Cutler, Christopher W.; Ji-hua Chen; PASHLEY David H.; Franklin R Tay

    2015-01-01

    Discoloration-resistant calcium aluminosilicate cement has been formulated to overcome the timely problem of tooth discoloration reported in the clinical application of bismuth oxide-containing hydraulic cements. The present study examined the effects of this experimental cement (Quick-Set2) on the viability and proliferation of human dental pulp stem cells (hDPSCs) by comparing the cellular responses with commercially available calcium silicate cement (white mineral trioxide aggregate; WMTA)...

  15. Behavior of calcium silicate hydrate in aluminate solution

    Institute of Scientific and Technical Information of China (English)

    LI Xiao-bin; ZHAO Zhuo; LIU Gui-hua; ZHOU Qiu-sheng; PENG Zhi-hong

    2005-01-01

    Using calcium hydroxide and sodium silicate as starting materials, two kinds of calcium silicate hydrates, CaO · SiO2 · H2O and 2CaO · SiO2 · 1.17H2O, were hydro-thermally synthesized at 120 ℃. The reaction rule of calcium silicate hydrate in aluminate solution was investigated. The result shows that CaO · SiO2 · H2O is more stable than 2CaO · SiO2 · 1.17H2 O in aluminate solution and its stability increases with the increase of reaction temperature but decreases with the increase of caustic concentration. The reaction between calcium silicate hydrate and aluminate solution is mainly through two routes. In the first case, Al replaces partial Si in calcium silicate hydrate, meanwhile 3CaO · Al2 O3 · xSiO2 · (6-2x) H2 O (hydro-garnet) is formed and some SiO2 enters the solution. In the second case, calcium silicate hydrate can react directly with aluminate solution, forming hydro-garnet and Na2O · Al2O3 · 2SiO2 · nH2O (DSP). The desilication reaction of aluminate solution containing silicate could contribute partially to forming DSP.

  16. Distribution of Water in Synthetic Calcium Silicate Hydrates.

    Science.gov (United States)

    Roosz, C; Gaboreau, S; Grangeon, S; Prêt, D; Montouillout, V; Maubec, N; Ory, S; Blanc, P; Vieillard, P; Henocq, P

    2016-07-12

    Understanding calcium silicate hydrates (CSHs) is of paramount importance for understanding the behavior of cement materials because they control most of the properties of these man-made materials. The atomic scale water content and structure have a major influence on their properties, as is analogous with clay minerals, and we should assess these. Here, we used a multiple analytical approach to quantify water distribution in CSH samples and to determine the relative proportions of water sorbed on external and internal (interlayer) surfaces. Water vapor isotherms were used to explain the water distribution in the CSH microstructure. As with many layered compounds, CSHs have external and internal (interlayer) surfaces displaying multilayer adsorption of water molecules on external surfaces owing to the hydrophilic surfaces. Interlayer water was also quantified from water vapor isotherm, X-ray diffraction (XRD), and thermal gravimetric analyses (TGA) data, displaying nonreversible swelling/shrinkage behavior in response to drying/rewetting cycles. From this quantification and balance of water distribution, we were able to explain most of the widely dispersed data already published according to the various relative humidity (RH) conditions and measurement techniques. Stoichiometric formulas were proposed for the different CSH samples analyzed (0.6 < Ca/Si < 1.6), considering the interlayer water contribution. PMID:27281114

  17. Preparation of Hollow Calcium Silicate Microparticles by Simple Emulsion

    OpenAIRE

    Eiichi Toorisaka; Syotaro Nagamatsu; Yasunobu Saruwatari; Makoto Hirata; Tadashi Hano

    2014-01-01

    Hollow calcium silicate microparticles were prepared by mixing a water-in-oil (W/O) emulsion containing silicate ions in aqueous phase with an oil phase containing a calcium/di-2-ethylhexyl phosphoric acid (D2EHPA) complex. The inorganic precipitation reaction at the oil-water interface was accelerated by using a simple W/O emulsion. Hollow microparticles were obtained when the mole ratio of D2EHPA and calcium in the oil phase was nearly 2:1. The shell formation of the par-ticles depended on ...

  18. The comparison between sulfate salt weathering of portland cement paste and calcium sulfoaluminate cement paste

    OpenAIRE

    Liu, Zanqun; Deng, Dehua; De Schutter, Geert

    2015-01-01

    In this paper, the damage performances of sulfate salt weathering of Portland cement paste and calcium sulfoaluminate (CSA) cement paste were compared according to authors' previous studies. It was found that the evaporation zone of speciments partially immersed in 10% Na2SO4 solution were both severely deteriorated for Portland cement and CSA cement. However, the differences were more significant: (1) the CSA cement paste were damaged just after 7 days exposure compared to the 5 months expos...

  19. Hydration water and microstructure in calcium silicate and aluminate hydrates

    International Nuclear Information System (INIS)

    Understanding the state of the hydration water and the microstructure development in a cement paste is likely to be the key for the improvement of its ultimate strength and durability. In order to distinguish and characterize the reacted and unreacted water, the single-particle dynamics of water molecules in hydrated calcium silicates (C3S, C2S) and aluminates (C3A, C4AF) were studied by quasi-elastic neutron scattering, QENS. The time evolution of the immobile fraction represents the hydration kinetics and the mobile fraction follows a non-Debye relaxation. Less sophisticated, but more accessible and cheaper techniques, like differential scanning calorimetry, DSC, and near-infrared spectroscopy, NIR, were validated through QENS results and they allow one to easily and quantitatively follow the cement hydration kinetics and can be widely applied on a laboratory scale to understand the effect of additives (i.e., superplasticizers, cellulosic derivatives, etc) on the thermodynamics of the hydration process. DSC provides information on the free water index and on the activation energy involved in the hydration process while the NIR band at 7000 cm-1 monitors, at a molecular level, the increase of the surface-interacting water. We report as an example the effect of two classes of additives widely used in the cement industry: superplasticizers, SPs, and cellulose derivatives. SPs interact at the solid surface, leading to a consistent increment of the activation energy for the processes of nucleation and growth of the hydrated phases. In contrast, the cellulosic additives do not affect the nucleation and growth activation energy, but cause a significant increment in the water availability: in other words the hydration process is more efficient without any modification of the solid/liquid interaction, as also evidenced by the 1H-NMR. Additional information is obtained by scanning electron microscopy (SEM), ultra small angle neutron scattering (USANS) and wide angle x

  20. Injectable bioactive calcium-magnesium phosphate cement for bone regeneration

    International Nuclear Information System (INIS)

    Novel injectable and degradable calcium-magnesium phosphate cement (CMPC) with rapid-setting characteristic was developed by the introduction of magnesium phosphate cement (MPC) into calcium phosphate cement (CPC). The calcium-magnesium phosphate cement prepared under the optimum P/L ratio exhibited good injectability and desired workability. It could set within 10 min at 37 0C in 100% relative humidity and the compressive strength could reach 47 MPa after setting for 48 h, indicating that the prepared cement has relatively high initial mechanical strength. The results of in vitro degradation experiments demonstrated the good degradability of the injectable CMPC, and its degradation rate occurred significantly faster than that of pure CPC in simulated body fluid (SBF) solution. It can be concluded that the novel injectable calcium-magnesium phosphate cement is highly promising for a wide variety of clinical applications, especially for the development of minimally invasive techniques.

  1. LABORATORY INVESTIGATIONS OF SILICATE MUD CONTAMINATION WITH CALCIUM

    Directory of Open Access Journals (Sweden)

    Nediljka Gaurina-Međimurec

    2004-12-01

    Full Text Available The silicate-based drilling fluid is a low solids KCl/polymer system with the addition of soluble sodium or potassium silicate to enhance inhibition and wellbore stability. Silicate-based drilling fluids exhibit remarkable shale and chalk stabilizing properties, resulting in gauge hole and the formation of firm cuttings when drilling reactive shales and soft chalks. Silicates protect shales by in-situ gellation when exposed to the neutral pore fluid and precipitation, which occurs on contact with divalent ions present at the surface of the shale. Also, silicates prevent the dispersion and washouts when drilling soft chalk by reacting with the Ca2+ ions present on chalk surfaces of cutting and wellbore to form a protective film. The silicate-based drilling fluid can be used during drilling hole section through shale interbeded anhydrite formations because of its superior shale stabilizing characteristics. However, drilling through the anhydrite can decrease the silicate concentration and change rheological and filtration fluid properties. So, the critical concentration of calcium ions should be investigated by lab tests. This paper details the mechanism of shale inhibition using silicate-based drilling fluid, and presents results of lab tests conducted to ascertain the effect of Ca2+ ions on silicate level in the fluid and the fluid properties.

  2. Leaching of nuclear waste glass in cement pore water: effect of calcium in solution

    International Nuclear Information System (INIS)

    In the French geological repository concept, intermediate-level vitrified wastes could be disposed of in a cement medium. The glass dissolution mechanisms and kinetics, expected to depend strongly on the chemical composition and pH of the leaching water, were studied in various cement pore water compositions corresponding to different stages of cement aging. In this study, we focused on the effects induced by cement pore water at equilibrium with respect to Portlandite (pH[25 C] = 12.4). A decrease in the maximum glass dissolution rate due to the effect of calcium was clearly observed compared to the reference medium, i.e. at the same pH in KOH solution. At higher reaction progress, calcium in solution was almost totally consumed after a few days, probably due to the formation of Calcium Silicate Hydrate (C-S-H) phases with silicon leached from the glass. Two assumptions can be proposed to explain the effect of calcium on the initial regime: either the calcium from solution reacts with silicon released to form a C-S-H passivating layer at the glass/solution interface, or calcium compensates two non-bridging oxygen (Si-O-) in the altered layer, which could decrease the hydrolysis of silicon bonds. (authors)

  3. Study of belite calcium sulfo-aluminate cement potential for zinc conditioning: From hydration to durability

    International Nuclear Information System (INIS)

    Calcium silicate cements are widely used for low- and intermediate-level radioactive waste conditioning. However, wastes produced by nuclear activities are very diverse and some of their components may chemically react with cement phases. For instance, ashes resulting from the incineration of technological wastes including neoprene and polyvinylchloride may contain substantial amounts of soluble zinc chloride. This compound is known to strongly delay or inhibit Portland cement setting. One approach to limit adverse cement-waste interactions is to select a binder showing a better compatibility with the waste while keeping cement matrix advantages (low cost, simple process, hydration with water provided by the waste...). This work thus investigates the potential of calcium sulfo-aluminate cement for zinc Zn(II) immobilization. Four aspects were considered: hydration (kinetics and products formed), properties of hydrated binders, mechanisms of zinc retention and durability of the cement pastes (based on leaching experiments and modelling). The influence of three main parameters was assessed: the gypsum content of the cement, the concentration of ZnCl2 and the thermal evolution at early age. It follows that materials based on a calcium sulfo-aluminate cement containing 20% gypsum are interesting candidates for zinc Zn(II) stabilization/solidification: there is no delay in hydration, mineralogy of the hydrated phases is slightly dependent on thermal history, mechanical strength is high, dimensional changes are limited and zinc Zn(II) is well immobilized, even if the cement paste is leached by pure water during a long period (90 d). (author)

  4. Final report on the safety assessment of aluminum silicate, calcium silicate, magnesium aluminum silicate, magnesium silicate, magnesium trisilicate, sodium magnesium silicate, zirconium silicate, attapulgite, bentonite, Fuller's earth, hectorite, kaolin, lithium magnesium silicate, lithium magnesium sodium silicate, montmorillonite, pyrophyllite, and zeolite.

    Science.gov (United States)

    Elmore, Amy R

    2003-01-01

    This report reviews the safety of Aluminum, Calcium, Lithium Magnesium, Lithium Magnesium Sodium, Magnesium Aluminum, Magnesium, Sodium Magnesium, and Zirconium Silicates, Magnesium Trisilicate, Attapulgite, Bentonite, Fuller's Earth, Hectorite, Kaolin, Montmorillonite, Pyrophyllite, and Zeolite as used in cosmetic formulations. The common aspect of all these claylike ingredients is that they contain silicon, oxygen, and one or more metals. Many silicates occur naturally and are mined; yet others are produced synthetically. Typical cosmetic uses of silicates include abrasive, opacifying agent, viscosity-increasing agent, anticaking agent, emulsion stabilizer, binder, and suspending agent. Clay silicates (silicates containing water in their structure) primarily function as adsorbents, opacifiers, and viscosity-increasing agents. Pyrophyllite is also used as a colorant. The International Agency for Research on Cancer has ruled Attapulgite fibers >5 microm as possibly carcinogenic to humans, but fibers Hectorite was nonirritating to the skin of rabbits in a Draize primary skin irritation study. Magnesium Aluminum Silicate and Sodium Magnesium Silicate caused minimal eye irritation in a Draize eye irritation test. Bentonite caused severe iritis after injection into the anterior chamber of the eyes of rabbits and when injected intralamellarly, widespread corneal infiltrates and retrocorneal membranes were recorded. In a primary eye irritation study in rabbits, Hectorite was moderately irritating without washing and practically nonirritating to the eye with a washout. Rats tolerated a single dose of Zeolite A without any adverse reaction in the eye. Calcium Silicate had no discernible effect on nidation or on maternal or fetal survival in rabbits. Magnesium Aluminum Silicate had neither a teratogenic nor adverse effects on the mouse fetus. Female rats receiving a 20% Kaolin diet exhibited maternal anemia but no significant reduction in birth weight of the pups was

  5. Production of precipitated calcium carbonate from calcium silicates and carbon dioxide

    International Nuclear Information System (INIS)

    The possibilities for reducing carbon dioxide emissions from the pulp and paper industry by calcium carbonation are presented. The current precipitated calcium carbonate (PCC) production uses mined, crushed calcium carbonate as raw materials. If calcium silicates were used instead, carbon dioxide emissions from the calcination of carbonates would be eliminated. In Finland, there could, thus, be a potential for eliminating 200 kt of carbon dioxide emissions per year, considering only the PCC used in the pulp and paper industry. A preliminary investigation of the feasibility to produce PCC from calcium silicates and the potential to replace calcium carbonate as the raw material was made. Calcium carbonate can be manufactured from calcium silicates by various methods, but only a few have been experimentally verified. The possibility and feasibility of these methods as a replacement for the current PCC production process was studied by thermodynamic equilibrium calculations using HSC software and process modelling using Aspen Plus[reg]. The results from the process modelling showed that a process that uses acetic acid for extraction of the calcium ions is a high potential option for sequestering carbon dioxide by mineral carbonation. The main obstacle seems to be the limited availability and relatively high price of wollastonite, which is a mineral with high calcium silicate content. An alternative is to use the more common, but also more complex, basalt rock instead

  6. In vitro macrophage cytotoxicity of five calcium silicates.

    OpenAIRE

    Skaug, V; Davies, R.; Gylseth, B

    1984-01-01

    Five calcium silicate minerals (two naturally occurring and three synthetic compounds) with defined morphology and chemical composition were compared for their cytotoxic and lysosomal enzyme releasing effects on unstimulated mouse peritoneal macrophages in vitro. One synthetic material, a fibrous tobermorite, was cytotoxic towards the cells, and two naturally occurring wollastonites induced selective release of beta-glucuronidase from the cells.

  7. SINTERING AND SULFATION OF CALCIUM SILICATE-ALUMINATE

    Science.gov (United States)

    The effect of sintering on the reactivity of solids at high temperature was studied. The nature of the interaction was studied with calcium silicate-aluminate reacting with SO2 between 665 and 800 C. The kinetics of the sintering and sulfation processes were measured independentl...

  8. Hydration and dimensional stability of calcium aluminate cement based systems

    OpenAIRE

    Bizzozero, Julien

    2014-01-01

    Calcium aluminate cements (CAC) are often used in combination with calcium sulfate and Portland cement for special applications where rapid setting, rapid drying and shrinkage compensation are required. A growing fraction of the clinker, which has the highest CO2 intensity, is being replaced by supplementary cementitious materials (SCM). These SCM are usually from industrial by-products such as slag, fly ashes or can simply be raw materials such as limestone. This project aims at replacing th...

  9. Structural models of random packing of spheres extended to bricks. Simulation of the nanoporous Calcium-Silicate-Hydrates.

    OpenAIRE

    Morales-Florez, Victor; BRUNET, Fabrice

    2009-01-01

    Abstract Structure simulation algorithms of random packing of spheres and bricks have been developed. These algorithms were used to reproduce the nanostructure of the cementitius calcium-silicate-hydrates. The textural parameters (specific surface area, porosity, pore size, etc.) of a C-S-H sample, the main binding phase of cements, have been derived from N2-physisorption experiments. In the same time, these parameters have been simulated by using a sphere-based structural model wh...

  10. Influence of the calcium sulfate source on the rheological behaviour of calcium sulfoaluminate cement pastes

    OpenAIRE

    Santacruz, Isabel; García-Maté, Marta; G. Aranda, Miguel Ángel; De la Torre, Ángeles G.

    2013-01-01

    Calcium sulfoaluminate (CSA) cements are receiving increasing attention since their manufacture produces much less CO2 than ordinary Portland cement (OPC) [1]. In addition, they show interesting properties such as high early-age strengths, short setting times and impermeability. The main uses of these CSA cements are for quick repairs and pre-cast products or floor concrete applications. They are prepared by mixing the clinker with different amounts of a calcium sulfate set regulator such as ...

  11. Potassium silicate and calcium silicate on the resistance of soybean to Phakopsora pachyrhizi infection

    OpenAIRE

    Maria Fernanda Cruz; Fabrício Ávila Rodrigues; Ana Paula Cardoso Diniz; Maurilio Alves Moreira; Everaldo Gonçalves de Barros

    2013-01-01

    The control of Asian Soybean Rust (ASR), caused by Phakopsora pachyrhizi, has been difficult due to the aggressiveness of the pathogen and the lack of resistant cultivars. The objective of this study was to evaluate the effects of spray of potassium silicate (PS) and soil amendment with calcium silicate (CS) on soybean resistance to ASR. The PS solution was sprayed to leaves 24 hours prior to fungal inoculation while CS was amended to the soil at thirty-five days before sowing. The infection ...

  12. Structural characterization of gel-derived calcium silicate systems.

    Science.gov (United States)

    Meiszterics, Anikó; Rosta, László; Peterlik, Herwig; Rohonczy, János; Kubuki, Shiro; Henits, Péter; Sinkó, Katalin

    2010-09-30

    The main aim of this study is to synthesize calcium silicate ceramics that exhibit suitable properties to be used for biomedical applications. In the present work, attention was paid to the understanding of processing-structure relationships. A particular effort was made to clarify the identification of Ca-O-Si bonds by means of spectroscopy. The calcium silicate systems were prepared via a sol-gel route, varying the chemical compositions, the catalyst concentration, and the temperature and time of aging and heat treatment. The processes and the phases evolved during the sol-gel procedure were determined. The bond systems were investigated by Fourier transform infrared (FTIR) and (29)Si magic angle spinning nuclear magnetic resonance (MAS NMR) spectroscopy and the aggregate structures by scanning electron microscopy (SEM), small-angle neutron scattering (SANS), small-angle X-ray scattering (SAXS), wide-angle X-ray scattering (WAXS), and X-ray diffraction (XRD) measurements. PMID:20828114

  13. Hydration of Blended Portland Cements Containing Calcium-Aluminosilicate Glass Powder and Limestone

    DEFF Research Database (Denmark)

    Moesgaard, Mette; Poulsen, S.L.; Herfort, D.;

    2012-01-01

    represents a potential alternative to traditional SCMs, used for reduction of the CO2 emission associated with cement production. It is found that the NCAS glass takes part in the hydration reactions after about two weeks of hydration and a degree of reaction of approx. 50 % is observed after 90 days of......This work investigates the hydration of blended Portland cement containing 30 wt.% Na2O-CaO-Al2O3-SiO2 (NCAS) glass particles either as the only supplementary cementitious material (SCM) or in combination with limestone, using 29Si MAS NMR, powder XRD, and thermal analyses. The NCAS glass...... hydration. The hydrated glass contributes to the formation of the calcium-silicate-hydrate (C-S-H) phase, consuming a part of the Portlandite (Ca(OH)2) formed during hydration of the Portland cement. Furthermore, the presence of the glass and limestone particles, alone or in combination, results in an...

  14. Solubility of a new calcium silicate-based root-end filling material

    Directory of Open Access Journals (Sweden)

    Shishir Singh

    2015-01-01

    Full Text Available Introduction: The purpose of this study was to compare solubility of a new calcium silicate-based cement, Biodentine with three commonly used root-end filling materials viz. glass-ionomer cement (GIC, intermediate restorative material (IRM, and mineral trioxide aggregate (MTA. Materials and Methods: Twenty stainless steel ring molds were filled with cements corresponding to four groups (n = 5. The weight of 20 dried glass bottles was recorded. Samples were transferred to bottles containing 5 ml of distilled water and stored for 24 h. The bottles were dried at 105΀C and weighed. This procedure was repeated for 3, 10, 30, and 60 days. Data was analyzed with one-way analysis of variance (ANOVA test (P < 0.05. Results: Biodentine demonstrated significantly higher solubility than MTA for 30- and 60-day immersion periods. Statistical difference was noted between the solubility values of Biodentine samples amongst each of the five time intervals. Conclusions: Biodentine exhibited higher solubility in comparison with all other cements.

  15. Preparation and fluorescence property of red-emitting Eu3+-activated amorphous calcium silicate phosphor

    International Nuclear Information System (INIS)

    This paper describes the energy efficient synthesis of a red-emitting Eu3+-activated amorphous calcium silicate phosphor produced by heating a Eu3+-activated calcium silicate hydrate phosphor. Concentration quenching of the Eu3+-activated calcium silicate hydrate phosphor was not observed and the emission intensity did not decrease up to a Eu/(Ca+Eu) atomic ratio of 0.46. Heating of the Eu3+-activated calcium silicate hydrate (Eu/(Ca+Eu) atomic ratio = 0.32) phosphor produced an amorphous Eu3+-activated calcium silicate phosphor, which had a maximum emission intensity at 870 oC and emitted in the red under near-ultraviolet irradiation (395 nm). The emission intensity of the Eu3+-activated amorphous calcium silicate phosphor was about half that of a commercial BaMgAl10O17:Eu2+ phosphor, and shows great potential for application in white light-emitting diodes.

  16. Hydration of Portland cement with additions of calcium sulfoaluminates

    Energy Technology Data Exchange (ETDEWEB)

    Le Saout, Gwenn, E-mail: gwenn.le-saout@mines-ales.fr [Empa, Swiss Federal Laboratories for Materials Science and Technology, Concrete and Construction Chemistry Laboratory, Ueberlandstrasse 129, CH-8600 Duebendorf (Switzerland); Lothenbach, Barbara [Empa, Swiss Federal Laboratories for Materials Science and Technology, Concrete and Construction Chemistry Laboratory, Ueberlandstrasse 129, CH-8600 Duebendorf (Switzerland); Hori, Akihiro [DENKA Chemicals GmbH, Wehrhahn-Center, Cantadorstr. 3, D-40211 Duesseldorf (Germany); Higuchi, Takayuki [Denki Kagaku Kogyo Kabushiki Kaisha (DENKA), Omi, Itoigawa, Niigata, 949-0393 (Japan); Winnefeld, Frank [Empa, Swiss Federal Laboratories for Materials Science and Technology, Concrete and Construction Chemistry Laboratory, Ueberlandstrasse 129, CH-8600 Duebendorf (Switzerland)

    2013-01-15

    The effect of mineral additions based on calcium aluminates on the hydration mechanism of ordinary Portland cement (OPC) was investigated using isothermal calorimetry, thermal analysis, X-ray diffraction, scanning electron microscopy, solid state nuclear magnetic resonance and pore solution analysis. Results show that the addition of a calcium sulfoaluminate cement (CSA) to the OPC does not affect the hydration mechanism of alite but controls the aluminate dissolution. In the second blend investigated, a rapid setting cement, the amorphous calcium aluminate reacts very fast to ettringite. The release of aluminum ions strongly retards the hydration of alite but the C-S-H has a similar composition as in OPC with no additional Al to Si substitution. As in CSA-OPC, the aluminate hydration is controlled by the availability of sulfates. The coupling of thermodynamic modeling with the kinetic equations predicts the amount of hydrates and pore solution compositions as a function of time and validates the model in these systems.

  17. Hydration of Portland cement with additions of calcium sulfoaluminates

    International Nuclear Information System (INIS)

    The effect of mineral additions based on calcium aluminates on the hydration mechanism of ordinary Portland cement (OPC) was investigated using isothermal calorimetry, thermal analysis, X-ray diffraction, scanning electron microscopy, solid state nuclear magnetic resonance and pore solution analysis. Results show that the addition of a calcium sulfoaluminate cement (CSA) to the OPC does not affect the hydration mechanism of alite but controls the aluminate dissolution. In the second blend investigated, a rapid setting cement, the amorphous calcium aluminate reacts very fast to ettringite. The release of aluminum ions strongly retards the hydration of alite but the C–S–H has a similar composition as in OPC with no additional Al to Si substitution. As in CSA–OPC, the aluminate hydration is controlled by the availability of sulfates. The coupling of thermodynamic modeling with the kinetic equations predicts the amount of hydrates and pore solution compositions as a function of time and validates the model in these systems.

  18. Rheological and hydration characterization of calcium sulfoaluminate cement pastes

    OpenAIRE

    García-Maté, Marta; Santacruz, Isabel; de la Torre, Ángeles G.; León-Reina, Laura; Aranda, Miguel A. G.

    2012-01-01

    Calcium sulfoaluminate (CSA) cements are currently receiving a lot of attention because their manufacture produces less CO2 than ordinary Portland cement (OPC). However, it is essential to understand all parameters which may affect the hydration processes. This work deals with the study of the effect of several parameters, such as superplasticizer (SP), gypsum contents (10, 20 and 30 wt%) and w/c ratio (0.4 and 0.5), on the properties of CSA pastes during early hydration. This characteriza...

  19. Evaluation of a porosity measurement method for wet calcium phosphate cements

    OpenAIRE

    Ajaxon, Ingrid; Maazouz, Yassine; Ginebra Molins, Maria Pau; Ohman, Caroline; Persson, Cecilia

    2015-01-01

    The porosity of a calcium phosphate cement is a key parameter as it affects several important properties of the cement. However, a successful, non-destructive porosity measurement method that does not include drying has not yet been reported for calcium phosphate cements. The aim of this study was to evaluate isopropanol solvent exchange as such a method. Two different types of calcium phosphate cements were used, one basic (hydroxyapatite) and one acidic (brushite). The cements were allowed ...

  20. Synthesis of Calcium Silicate (Casio3 Using Calcium Fluoride, Quartz and Microbes

    Directory of Open Access Journals (Sweden)

    B. Gopal Krishna

    2015-09-01

    Full Text Available Microbes like bacteria, algae, fungi and virus play an important role to catalyst chemical reactions. In Nature, ores or minerals of different compounds are formed due to microbial environment and other factors like weathering. Microbial environment is also instrumental in forming calcium containing silicate minerals. Chemical reactions occur under microbial environment because microbes have the ability to control or modify different factors like pH, chemical potential and temperature during reactions. In this paper, synthesis of calcium silicate (CaSiO3 using calcium fluoride (CaF2 and quartz (SiO2 under microbial environment in a laboratory is being adopted to produce the required material. XRD technique is used to confirm the formation of CaSiO3.

  1. Hydration of calcium sulfoaluminate cements - Experimental findings and thermodynamic modelling

    International Nuclear Information System (INIS)

    Calcium sulfoaluminate cements (CSA) are a promising low-CO2 alternative to ordinary Portland cements and are as well of interest concerning their use as binder for waste encapsulation. In this study, the hydration of two CSA cements has been investigated experimentally and by thermodynamic modelling between 1 h and 28 days at w/c ratios of 0.72 and 0.80, respectively. The main hydration product of CSA is ettringite, which precipitates together with amorphous Al(OH)3 until the calcium sulfate is consumed after around 1-2 days of hydration. Afterwards, monosulfate is formed. In the presence of belite, straetlingite occurs as an additional hydration product. The pore solution analysis reveals that straetlingite can bind a part of the potassium ions, which are released by the clinker minerals. The microstructure of both cements is quite dense even after 16 h of hydration, with not much pore space available at a sample age of 28 days. The pore solution of both cements is dominated during the first hours of hydration by potassium, sodium, calcium, aluminium and sulfate; the pH is around 10-11. When the calcium sulfate is depleted, the sulfate concentration drops by a factor of 10. This increases pH to around 12.5-12.8. Based on the experimental data, a thermodynamic hydration model for CSA cements based on cement composition, hydration kinetics of clinker phases and calculations of thermodynamic equilibria by geochemical speciation has been established. The modelled phase development with ongoing hydration agrees well with the experimental findings.

  2. Cementing properties of steel slag activated by sodium silicates and sodium hydroxide

    Institute of Scientific and Technical Information of China (English)

    Wen Ni; En Wang; Jianping Li; Han Sun

    2005-01-01

    Steel slag which is mainly composed of γ-CasSiO4 and other silicates or alumino-silicates is activated by sodium silicates and sodium hydroxide. The powders of such steel slag are usually inert to hydrate and subsequently have very low ability of cementing. But when sodium silicates and sodium hydroxide are used as activators the steel slag shows very good properties of cementing. When activated with NaOH solution the hardened slurry of the steel slag has a compressive strength of 11.13 MPa after being cured for 28 days. When activated with Na2SiO3 solution the samples after being cured for 28 days have an average compressive strength of 40.23 MPa. While the steel slag slurry which is only mixed with water has a compressive of 0.88 MPa after being cured for 28 days.

  3. Influence of ferrite phase in alite-calcium sulfoaluminate cements

    Science.gov (United States)

    Duvallet, Tristana Yvonne Francoise

    Since the energy crisis in 1970's, research on low energy cements with low CO2- emissions has been increasing. Numerous solutions have been investigated, and the goal of this original research is to create a viable hybrid cement with the components of both Ordinary Portland cement (OPC) and calcium sulfoaluminate cement (CSAC), by forming a material that contains both alite and calcium sulfoaluminate clinker phases. Furthermore, this research focuses on keeping the cost of this material reasonable by reducing aluminum requirements through its substitution with iron. The aim of this work would produce a cement that can use large amounts of red mud, which is a plentiful waste material, in place of bauxite known as an expensive raw material. Modified Bogue equations were established and tested to formulate this novel cement with different amounts of ferrite, from 5% to 45% by weight. This was followed by the production of cement from reagent chemicals, and from industrial by-products as feedstocks (fly ash, red mud and slag). Hydration processes, as well as the mechanical properties, of these clinker compositions were studied, along with the addition of gypsum and the impact of a ferric iron complexing additive triisopropanolamine (TIPA). To summarize this research, the influence of the addition of 5-45% by weight of ferrite phase, was examined with the goal of introducing as much red mud as possible in the process without negatively attenuate the cement properties. Based on this PhD dissertation, the production of high-iron alite-calcium sulfoaluminateferrite cements was proven possible from the two sources of raw materials. The hydration processes and the mechanical properties seemed negatively affected by the addition of ferrite, as this phase was not hydrated entirely, even after 6 months of curing. The usage of TIPA counteracted this decline in strength by improving the ferrite hydration and increasing the optimum amount of gypsum required in each composition

  4. Dissolution-precipitation behaviour of ettringite, monosulfate, and calcium silicate hydrate

    International Nuclear Information System (INIS)

    The stability of the cement minerals ettringite, monosulfate, and calcium silicate hydrate (C-S-H) was investigated to better understand the uptake of contaminants in waste-cement mixes. Suspensions were spiked with radioisotopes of components (45Ca and 35SO4 for ettringite and monosulfate and 45Ca and 32Si for C-S-H) to observe their uptake behaviour within 0-70 days. A physical model was applied to determine dissolution-precipitation rates. An initial fast uptake was observed to occur in most systems, so the data obtained between 7 and 70 days were chosen for analysis. Dissolution-precipitation rates were in the range of 10-11.5 to 10-12.2 mol m-2 s-1 for all minerals. The whole solids would be dissolved and reprecipitated within 1-4 years. The measured dissolution-precipitation rates of pure cement minerals give the maximum rate for ion substitution processes with contaminants and are distinguishable from faster processes such as surface complexation and ion exchange processes

  5. Microstructure engineering of Portland cement pastes and mortars through addition of ultrafine layer silicates

    DEFF Research Database (Denmark)

    Lindgreen, Holger; Geiker, Mette Rica; Krøyer, Hanne;

    2008-01-01

    Pozzolanic submicron-sized silica fume and the non-pozzolanic micron- and nano-sized layer silicates (clay minerals) kaolinite, smectite and palygorskite have been used as additives in Portland cement pastes and mortars. These layer silicates have different particle shape (needles and plates......, in comparison to the pure cement pasta and the paste containing kaolinite, a more open pore structure consisting of fine pores. Silica fume paste contains a significant amount of closed pores. As a secondary result, it is demonstrated that both the degree and duration of sample drying strongly modifies...

  6. Calcium silicate hydrates: Solid and liquid phase composition

    International Nuclear Information System (INIS)

    This paper presents a review on the relationship between the composition, the structure and the solution in which calcium silicate hydrate (C–S–H) is equilibrated. The silica chain length in C–S–H increases with the silicon concentration and the calcium content in the interlayer space with the calcium concentrations. Sodium and potassium are taken up in the interlayer space, preferentially at low calcium concentrations and thus by low Ca/Si C–S–H. Aluminium uptake in C–S–H increases strongly at higher aluminium concentrations in the solution. At low Ca/Si, aluminium substitutes silica in the bridging position, at Ca/Si > 1 aluminium is bound in TAH. Recently developed thermodynamic models are closely related to the structure of C–S–H and tobermorite, and able to model not only the solubility and the chemical composition of the C–S–H, but also to predict the mean silica chain length and the uptake of aluminium

  7. Calcium silicate hydrates: Solid and liquid phase composition

    Energy Technology Data Exchange (ETDEWEB)

    Lothenbach, Barbara, E-mail: Barbara.lothenbach@empa.ch [Laboratory Concrete & Construction Chemistry, Empa (Switzerland); Nonat, André [ICB, UMR CNRS 6303 CNRS-Université de Bourgogne, Faculté des Sciences et Techniques, BP47870, 21078 Dijon Cedex (France)

    2015-12-15

    This paper presents a review on the relationship between the composition, the structure and the solution in which calcium silicate hydrate (C–S–H) is equilibrated. The silica chain length in C–S–H increases with the silicon concentration and the calcium content in the interlayer space with the calcium concentrations. Sodium and potassium are taken up in the interlayer space, preferentially at low calcium concentrations and thus by low Ca/Si C–S–H. Aluminium uptake in C–S–H increases strongly at higher aluminium concentrations in the solution. At low Ca/Si, aluminium substitutes silica in the bridging position, at Ca/Si > 1 aluminium is bound in TAH. Recently developed thermodynamic models are closely related to the structure of C–S–H and tobermorite, and able to model not only the solubility and the chemical composition of the C–S–H, but also to predict the mean silica chain length and the uptake of aluminium.

  8. Bioactivity studies of calcium magnesium silicate prepared from eggshell waste by sol–gel combustion synthesis

    Directory of Open Access Journals (Sweden)

    Rajan Choudhary

    2015-06-01

    Full Text Available The present study focused on the synthesis of calcium magnesium silicate (akermanite, Ca2MgSi2O7 using eggshell biowaste (as calcium source, magnesium nitrate and tetraethyl orthosilicate (TEOS as starting materials. Sol–gel combustion method was adopted to obtain calcium magnesium silicate. Citric acid was used as a fuel (reducing agent and nitrate ions present in the metal nitrates acts as an oxidizing agent during combustion process. The characterization of synthesized calcium magnesium silicate was carried out by powder X-ray diffraction (XRD, Fourier transform infrared (FTIR and scanning electron microscopy (SEM techniques. Calcium magnesium silicate crystallite size was observed in nano regime which can effectively mimic natural bone apatite composition. In-vitro bioactivity was investigated by immersing calcium magnesium silicate pellet in simulated body fluid (SBF for three weeks. Results show effective deposition of crystallized hydroxyapatite (HAP layer on its surface and predicting its possibilities for applications in hard tissue regeneration.

  9. Bioactivity studies of calcium magnesium silicate prepared from eggshell waste by sol–gel combustion synthesis

    OpenAIRE

    Rajan Choudhary; Sivasankar Koppala; Sasikumar Swamiappan

    2015-01-01

    The present study focused on the synthesis of calcium magnesium silicate (akermanite, Ca2MgSi2O7) using eggshell biowaste (as calcium source), magnesium nitrate and tetraethyl orthosilicate (TEOS) as starting materials. Sol–gel combustion method was adopted to obtain calcium magnesium silicate. Citric acid was used as a fuel (reducing agent) and nitrate ions present in the metal nitrates acts as an oxidizing agent during combustion process. The characterization of synthesized calcium magnesiu...

  10. A low-temperature sol-gel route for the synthesis of bioactive calcium silicates

    Institute of Scientific and Technical Information of China (English)

    Yong-Sen Sun; Ai-Ling Li; Fu-Jian Xu; Dong Qiu

    2013-01-01

    Sol-gel-derived bioactive calcium silicates,synthesized from calcium nitrate tetrahydrate and calcium 2-methoxyethoxide as calcium precursor respectively,were calcified under different temperatures.A series of techniques including SEM,TGA,solid 29Si NMR,nitrogen adsorption,and simulated body fluids (SBF) soaking were employed to study their textural features and in vitro bioactivity.It was confirmed that calcium 2-methoxyethoxide is a promising candidate of calcium precursor for bioactive calcium silicates stabilized under low temperatures.This has implications in fabrication of organic-inorganic hybrid composites.

  11. Application of reference point indentation for micro-mechanical surface characterization of calcium silicate based dental materials.

    Science.gov (United States)

    Antonijević, Djordje; Milovanović, Petar; Riedel, Christoph; Hahn, Michael; Amling, Michael; Busse, Björn; Djurić, Marija

    2016-04-01

    The objective of this study was to elucidate micromechanical properties of Biodentine and two experimental calcium silicate cements (CSCs) using Reference Point Indentation (RPI). Biomechanical characteristics of the cement type and the effects of a radiopacifier, liquid components, acid etching treatment and bioactivation in simulated body fluid (SBF) were investigated by measuring the microhardness, average unloading slope (Avg US) and indentation distance increase (IDI). Biodentine had a greater microhardness than the experimental CSCs, while the Avg US and IDI values were not significantly different among investigated materials. There was a statistically significant difference in microhardness and IDI values between pure CSCs and radiopacified cements (p < 0.05). Micromechanical properties were not affected by different liquid components used. Acid-etching treatment reduced Biodentine's microhardness while cements' immersion in SBF resulted in greater microhardness and higher IDI values compared to the control group. Clearly, the physiological environment and the cements' composition affect their surface micromechanical properties. The addition of calcium chloride and CSCs' immersion in SBF are beneficial for CSCs' micromechanical performance, while the addition of radiopacifiers and acid etching treatment weaken the CSCs' surface. Application of RPI aids with the characterization of micromechanical properties of synthetic materials' surfaces. PMID:26888441

  12. Synthesis and reaction behavior of calcium silicate hydrate in basic system

    Institute of Scientific and Technical Information of China (English)

    刘桂华; 贺强; 李小斌; 彭志宏; 周秋生

    2004-01-01

    At the molar ratio of CaO to SiO2 of 1, with calcium hydroxide and sodium silicate, calcium silicate hydrate was synthesized at 50, 100, 170 ℃, respectively. The results show that temperature favors the formation of calcium silicate hydrate with perfect structure. When calcium silicate hydrate reacts with caustic solution, the decomposition rate of calcium silicate hydrate increases with the increasing caustic concentration and decreases with the raising synthesis temperature and the prolongation of reaction time. The decomposition rate is all less than 1.2 % in caustic solution, and XRD pattern of the residue after reaction with caustic solution is found as the same as that of original calcium silicate hydrate, which indicates the stable existence of calcium silicate hydrate in caustic solution.When reacted with soda solution, the decomposition rate increases with the increasing soda concentration and reaction time, while decreases with the synthesis temperature. The decomposition rate is more than 2% because CaO · SiO2 · H2O(CSH( Ⅰ )), except Ca5 (OH)2Si6O16 · 4H2O and Ca6Si6O17 (OH)2, is decomposed. So the synthesis temperature and soda concentration should be controlled in the process of transformation of sodium aluminosilicate hydrate into calcium silicate hydrate.

  13. Productivity and nutritive value of bluestem grass fertilized with calcium and magnesium silicate

    OpenAIRE

    Cinthya Souza Santana; Laura Souza Santos; Greiciele de Morais; Luiz Arnaldo Fernandes; Luciana Castro Geraseev

    2016-01-01

    This study evaluated the effect of application of calcium and magnesium silicate on the productivity, chemical composition and in situ ruminal degradation of bluestem grass (Andropogon gayanus Kunth, cv. Baeti; Embrapa 23) during the rainy and dry seasons. The design consisted of completely randomized blocks in a 6x2 factorial scheme (six silicate doses and two cutting seasons), arranged in plots subdivided over time. The plots were the calcium and magnesium silicate doses (0, 200, 400, 600, ...

  14. Preparation of TiO2 nanotubes/mesoporous calcium silicate composites with controllable drug release.

    Science.gov (United States)

    Xie, Chunling; Li, Ping; Liu, Yan; Luo, Fei; Xiao, Xiufeng

    2016-10-01

    Nanotube structures such as TiO2 nanotube (TNT) arrays produced by self-ordering electrochemical anodization have been extensively explored for drug delivery applications. In this study, we presented a new implantable drug delivery system that combined mesoporous calcium silicate coating with nanotube structures to achieve a controllable drug release of water soluble and antiphlogistic drug loxoprofen sodium. The results showed that the TiO2 nanotubes/mesoporous calcium silicate composites were successfully fabricated by a simple template method and the deposition of mesoporous calcium silicate increased with the soaking time. Moreover, the rate of deposition of biological mesoporous calcium silicate on amorphous TNTs was better than that on anatase TNTs. Further, zinc-incorporated mesoporous calcium silicate coating, produced by adding a certain concentration of zinc nitrate into the soaking system, displayed improved chemical stability. A significant improvement in the drug release characteristics with reduced burst release and sustained release was demonstrated. PMID:27287140

  15. Synthesis of Calcium Silicate (Casio3) Using Calcium Fluoride, Quartz and Microbes

    OpenAIRE

    B. Gopal Krishna; M. Jagannadha Rao

    2015-01-01

    Microbes like bacteria, algae, fungi and virus play an important role to catalyst chemical reactions. In Nature, ores or minerals of different compounds are formed due to microbial environment and other factors like weathering. Microbial environment is also instrumental in forming calcium containing silicate minerals. Chemical reactions occur under microbial environment because microbes have the ability to control or modify different factors like pH, chemical potential and tempera...

  16. EFFECT OF QUARTZ/MULLITE BLEND CERAMIC ADDITIVE ON IMPROVING RESISTANCE TO ACID OF SODIUM SILICATE-ACTIVATED SLAG CEMENT. CELCIUS BRINE.

    Energy Technology Data Exchange (ETDEWEB)

    SUGAMA, T.; BROTHERS, L.E.; VAN DE PUTTE, T.R.

    2006-06-01

    We evaluated the usefulness of manufactured quartz/mullite blend (MQMB) ceramic powder in increasing the resistance to acid of sodium silicate-activated slag (SSAS) cementitious material for geothermal wells. A 15-day exposure to 90{sup o} CO{sub 2}-laden H{sub 2}SO{sub 4} revealed that the MQMB had high potential as an acid-resistant additive for SSAS cement. Two factors, the appropriate ratio of slag/MQMB and the autoclave temperature, contributed to better performance of MQMB-modified SSAS cement in abating its acid erosion. The most effective slag/MQMB ratio in minimizing the loss in weight by acid erosion was 70/30 by weight. For autoclave temperature, the loss in weight of 100 C autoclaved cement was a less than 2%, but at 300 C it was even lower. Before exposure to acid, the cement autoclaved at 100 C was essentially amorphous; increasing the temperature to 200 C led to the formation of crystalline analcime in the zeolitic mineral family during reactions between the mullite in MQMB and the Na from sodium silicate. In addition, at 300 C, crystal of calcium silicate hydrate (1) (CSH) was generated in reactions between the quartz in MQMB and the activated slag. These two crystalline phases (CSH and analcime) were responsible for densifying the autoclaved cement, conveying improved compressive strength and minimizing water permeability. The CSH was susceptible to reactions with H{sub 2}SO{sub 4}, forming two corrosion products, bassanite and ionized monosilicic acid. However, the uptake of ionized monosilicic acid by Mg dissociated from the activated slag resulted in the formation of lizardite as magnesium silicate hydrate. On the other hand, the analcime was barely susceptible to acid if at all. Thus, the excellent acid resistance of MQMB-modified SSAS cement was due to the combined phases of lizardite and analcime.

  17. Silver-Doped Calcium Phosphate Bone Cements with Antibacterial Properties

    Science.gov (United States)

    Rau, J. V.; Fosca, M.; Graziani, V.; Egorov, A. A.; Zobkov, Yu. V.; Fedotov, A. Yu.; Ortenzi, M.; Caminiti, R.; Baranchikov, A. E.; Komlev, V. S.

    2016-01-01

    Calcium phosphate bone cements (CPCs) with antibacterial properties are demanded for clinical applications. In this study, we demonstrated the use of a relatively simple processing route based on preparation of silver-doped CPCs (CPCs-Ag) through the preparation of solid dispersed active powder phase. Real-time monitoring of structural transformations and kinetics of several CPCs-Ag formulations (Ag = 0 wt %, 0.6 wt % and 1.0 wt %) was performed by the Energy Dispersive X-ray Diffraction technique. The partial conversion of β-tricalcium phosphate (TCP) phase into the dicalcium phosphate dihydrate (DCPD) took place in all the investigated cement systems. In the pristine cement powders, Ag in its metallic form was found, whereas for CPC-Ag 0.6 wt % and CPC-Ag 1.0 wt % cements, CaAg(PO3)3 was detected and Ag (met.) was no longer present. The CPC-Ag 0 wt % cement exhibited a compressive strength of 6.5 ± 1.0 MPa, whereas for the doped cements (CPC-Ag 0.6 wt % and CPC-Ag 1.0 wt %) the reduced values of the compressive strength 4.0 ± 1.0 and 1.5 ± 1.0 MPa, respectively, were detected. Silver-ion release from CPC-Ag 0.6 wt % and CPC-Ag 1.0 wt % cements, measured by the Atomic Emission Spectroscopy, corresponds to the average values of 25 µg/L and 43 µg/L, respectively, rising a plateau after 15 days. The results of the antibacterial test proved the inhibitory effect towards pathogenic Escherichia coli for both CPC-Ag 0.6 wt % and CPC-Ag 1.0 wt % cements, better performances being observed for the cement with a higher Ag-content. PMID:27096874

  18. Synthesis of pure zeolite P2 from calcium silicate hydrate; tobermorite

    OpenAIRE

    Nasser Y. Mostafa; Rasha A. Garib; Z. K. Heiba; Abd-Elkader, Omar H.; M. M. Al-Majthoub

    2015-01-01

    Calcium silicate hydrate phases offer the possibility to become potential zeolites precursors due to its high silica contents. Pure calcium silicate hydrate phase; tobermorite (Ca5Si6O16(OH)2·4H2O), was prepared by hydrothermal method at 175°C. Tobermorite was sucssefully converted to Zeolite P2 for the first time via refluxing in 3 M NaOH solution and in the presence of Al source. Sodium hydroxide removed calcium ions from the interlayers of calcium silicate phase and form mesoporous zeolite...

  19. Changes on the nanostructure of cementitius calcium silicate hydrates (C-S-H) induced by aqueous carbonation

    OpenAIRE

    Morales-Florez, Víctor; Findling, N.; F. Brunet

    2015-01-01

    The nanostructure of the main binding phase of the hydrated cements, the calcium silicate hydrates (C-S-H), and their structural changes due to aqueous carbonation have been characterized using TEM, nitrogen physisorption, and SAXS. Synthetic C-S-H has been used for this purpose. Two different morphologies were identified, similar to the high density and low density C-S-H types. When submitting the sample to a CO 2 flux, the low density phase was completely carbonated. The carbonation by-prod...

  20. Synthesis and Characterization of Different Crystalline Calcium Silicate Hydrate: Application for the Removal of Aflatoxin B1 from Aqueous Solution

    OpenAIRE

    Lu Zeng; Ligang Yang; Shuping Wang; Kai Yang

    2014-01-01

    Different crystalline calcium silicate hydrates (CSH) were synthesized under specific hydrothermal conditions and several methods were used to analyze samples. Amorphous calcium silicate hydrates (ACSH) mainly consists of disordered calcium silicate hydrate gel (C-S-H gel) and crystalline calcium silicate hydrates (CCSH) consists of crystallized tobermorite. The adsorption of carcinogenic aflatoxin B1 (AFB1) onto ACSH and CCSH was investigated. The adsorption kinetics was studied using pseudo...

  1. Furcal perforation repair using calcium enriched mixture cement

    Directory of Open Access Journals (Sweden)

    Asgary Saeed

    2010-01-01

    Full Text Available This case describes a furcal perforation in a mandibular first molar accompanied by furcal lesion which has been managed after one month. Root canal treatment was performed; subsequently, the defect was repaired with calcium enriched mixture (CEM cement. The endodontically treated tooth was restored with amalgam. A 24-month recall showed no evidence of periodontal breakdown, no symptoms, in addition to completes healing of furcal lesion. According to physical and biological properties of the newly introduced CEM cement, this novel material may be suitable for sealing and repairing the perforations. The present case report supports this hypothesis.

  2. Accelerated carbonation of Friedel's salt in calcium aluminate cement paste

    International Nuclear Information System (INIS)

    The stability of Friedel's salt with respect to carbonation has been studied in calcium aluminate cement (CAC) pastes containing NaCl (3% of Cl- by weight of cement). Carbonation was carried out on a powdered sample in flowing 5% CO2 gas at 65% relative humidity to accelerate the process. At an intermediate carbonation step, a part of the sample was washed and dried up to 10 cycles to simulate a dynamic leaching attack. The two processes were followed by means of X-ray diffraction (XRD), pH and Cl- analyses in the simulated pore solution

  3. Discrete element modeling of calcium-silicate-hydrate

    International Nuclear Information System (INIS)

    The discrete element method (DEM) was used to model calcium-silicate-hydrate (C-S-H) at the nanoscale. The C-S-H nanoparticles were modeled as spherical particles with diameters of approximately 5 nm. Interparticle forces included traditional mechanical contact forces, van der Waals forces and ionic correlation forces due to negatively charged C-S-H nanoparticles and ion species in the nanopores. Previous work by the authors demonstrated the DEM method was feasible in studying the properties of the C-S-H nanostructures. In this work, the simulations were performed to look into the effects of nanoparticle packing, nanoparticle morphology, interparticle forces and nanoparticle properties on the deformation mechanisms and mechanical properties of the C-S-H matrix. This work will provide insights into possible ways to improve the properties of the C-S-H matrix. (paper)

  4. Thermodynamics and kinetics of the sulfation of porous calcium silicate

    Science.gov (United States)

    Miller, R. A.; Kohl, F. J.

    1981-01-01

    The sulfation of plasma sprayed calcium silicate in flowing SO2/air mixtures at 900 and 1000 C was investigated thermogravimetrically. Reaction products were analyzed using electron microprobe and X-ray diffraction analysis techniques, and results were compared with thermodynamic predictions. The percentage, by volume, of SO2 in air was varied between 0.036 and 10 percent. At 10 percent SO2 the weight gain curve displays a concave downward shoulder early in the sulfation process. An analytical model was developed which treats the initial process as one which decays exponentially with increasing time and the subsequent process as one which decays exponentially with increasing weight gain. At lower SO2 levels the initial rate is controlled by the reactant flow rate. At 1100 C and 0.036 percent SO2 there is no reaction, in agreement with thermodynamic predictions.

  5. Properties of Chemically Combusted Calcium Carbide Residue and Its Influence on Cement Properties

    Directory of Open Access Journals (Sweden)

    Hongfang Sun

    2015-02-01

    Full Text Available Calcium carbide residue (CCR is a waste by-product from acetylene gas production. The main component of CCR is Ca(OH2, which can react with siliceous materials through pozzolanic reactions, resulting in a product similar to those obtained from the cement hydration process. Thus, it is possible to use CCR as a substitute for Portland cement in concrete. In this research, we synthesized CCR and silica fume through a chemical combustion technique to produce a new reactive cementitious powder (RCP. The properties of paste and mortar in fresh and hardened states (setting time, shrinkage, and compressive strength with 5% cement replacement by RCP were evaluated. The hydration of RCP and OPC (Ordinary Portland Cement pastes was also examined through SEM (scanning electron microscope. Test results showed that in comparison to control OPC mix, the hydration products for the RCP mix took longer to formulate. The initial and final setting times were prolonged, while the drying shrinkage was significantly reduced. The compressive strength at the age of 45 days for RCP mortar mix was found to be higher than that of OPC mortar and OPC mortar with silica fume mix by 10% and 8%, respectively. Therefore, the synthesized RCP was proved to be a sustainable active cementitious powder for the strength enhanced of building materials, which will result in the diversion of significant quantities of this by-product from landfills.

  6. On the development of an apatitic calcium phosphate bone cement

    Indian Academy of Sciences (India)

    Manoj Komath; H K Varma; R Sivakumar

    2000-04-01

    Development of an apatitic calcium phosphate bone cement is reported. 100 Particles of tetracalcium phosphate (TTCP) and dicalcium phosphate dihydrate (DCPD) were mixed in equimolar ratio to form the cement powder. The wetting medium used was distilled water with Na2HPO4 as accelerator to manipulate the setting time. The cement powder, on wetting with the medium, formed a workable putty. The setting times of the putty were measured using a Vicat type apparatus and the compressive strength was determined with a Universal Testing Machine. The nature of the precipitated cement was analyzed through X-ray diffraction (XRD), fourier transform infrared spectrometry (FTIR) and energy dispersive electron microprobe (EDAX). The results showed the phase to be apatitic with a calcium–to–phosphorous ratio close to that of hydroxyapatite. The microstructure analysis using scanning electron microscopy (SEM) showed hydroxyapatite nanocrystallite growth over particulate matrix surface. The structure has an apparent porosity of ∼ 52%. There were no appreciable dimensional or thermal changes during setting. The cement passed the in vitro toxicological screening (cytotoxicity and haemolysis) tests. Optimization of the cement was done by manipulating the accelerator concentration so that the setting time, hardening time and the compressive strength had clinically relevant values.

  7. Cytotoxicity, calcium release, and pH changes generated by novel calcium phosphate cement formulations.

    Science.gov (United States)

    Khashaba, Rania M; Lockwood, Petra E; Lewis, Jill B; Messer, Regina L; Chutkan, Norman B; Borke, James L

    2010-05-01

    Few published studies describe the biological properties of calcium phosphate cements (CPCs) for dental applications. We measured several biologically relevant properties of 3 CPCs over an extended (8 wk) interval. Monocalcium phosphate, calcium oxide, and synthetic hydroxyapatite were combined with either modified polyacrylic acid, light-activated modified polyalkenoic acid, or 35% w/w polymethyl vinyl ether maleic acid to obtain Types I, II, and III CPCs, respectively. Set cements were placed in direct contact with L929 fibroblasts for up to 8 weeks. Media Ca(+2) and pH were determined by atomic absorption spectroscopy and pH electrode respectively. Cell mitochondrial function was measured by MTT assay. Type I cements suppressed mitochondrial activity > 90% (vs. Teflon controls), but significantly (p 90% at all times. Type III cements elevated mitochondrial activity significantly after 7 wks. The pH profiles approached neutrality by 24 h, and all cements released calcium into the storage medium at all periods (24 h - 8 wk). We concluded that several types of cements had long-term biological profiles that show promise for dental applications. PMID:20235188

  8. Potassium silicate and calcium silicate on the resistance of soybean to Phakopsora pachyrhizi infection

    Directory of Open Access Journals (Sweden)

    Maria Fernanda Cruz

    2013-01-01

    Full Text Available The control of Asian Soybean Rust (ASR, caused by Phakopsora pachyrhizi, has been difficult due to the aggressiveness of the pathogen and the lack of resistant cultivars. The objective of this study was to evaluate the effects of spray of potassium silicate (PS and soil amendment with calcium silicate (CS on soybean resistance to ASR. The PS solution was sprayed to leaves 24 hours prior to fungal inoculation while CS was amended to the soil at thirty-five days before sowing. The infection process of P. pachyrhizi was investigated by scanning electron microscopy. The uredia on leaves of plants sprayed with PS were smaller and more compact than those observed on the leaves of plants grown in soil amended with CS or in soil non-amended with CS (control treatment. On leaves of plants from the control treatment, uredia produced many urediniospores at 9 days after inoculation, and the ASR severity was 15, 8 and 9%, respectively, for plants from control, PS and CS treatments. In conclusion, the spray of PS contributed to reduce the number of uredia per cm² of leaf area and both PS spray and CS resulted in lower ASR symptoms.

  9. Mechanical behavior of a composite interface: Calcium-silicate-hydrates

    Energy Technology Data Exchange (ETDEWEB)

    Palkovic, Steven D.; Moeini, Sina; Büyüköztürk, Oral, E-mail: obuyuk@mit.edu [Department of Civil and Environmental Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 (United States); Yip, Sidney [Department of Nuclear Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 (United States)

    2015-07-21

    The generalized stacking fault (GSF) is a conceptual procedure historically used to assess shear behavior of defect-free crystalline structures through molecular dynamics or density functional theory simulations. We apply the GSF technique to the spatially and chemically complex quasi-layered structure of calcium-silicate-hydrates (C-S-H), the fundamental nanoscale binder within cementitious materials. A failure plane is enforced to calculate the shear traction-displacement response along a composite interface containing highly confined water molecules, hydroxyl groups, and calcium ions. GSF simulations are compared with affine (homogeneous) shear simulations, which allow strain to localize naturally in response to the local atomic environment. Comparison of strength and deformation behavior for the two loading methods shows the composite interface controls bulk shear deformation. Both models indicate the maximum shear strength of C-S-H exhibits a normal-stress dependency typical of cohesive-frictional materials. These findings suggest the applicability of GSF techniques to inhomogeneous structures and bonding environments, including other layered systems such as biological materials containing organic and inorganic interfaces.

  10. Mechanical behavior of a composite interface: Calcium-silicate-hydrates

    International Nuclear Information System (INIS)

    The generalized stacking fault (GSF) is a conceptual procedure historically used to assess shear behavior of defect-free crystalline structures through molecular dynamics or density functional theory simulations. We apply the GSF technique to the spatially and chemically complex quasi-layered structure of calcium-silicate-hydrates (C-S-H), the fundamental nanoscale binder within cementitious materials. A failure plane is enforced to calculate the shear traction-displacement response along a composite interface containing highly confined water molecules, hydroxyl groups, and calcium ions. GSF simulations are compared with affine (homogeneous) shear simulations, which allow strain to localize naturally in response to the local atomic environment. Comparison of strength and deformation behavior for the two loading methods shows the composite interface controls bulk shear deformation. Both models indicate the maximum shear strength of C-S-H exhibits a normal-stress dependency typical of cohesive-frictional materials. These findings suggest the applicability of GSF techniques to inhomogeneous structures and bonding environments, including other layered systems such as biological materials containing organic and inorganic interfaces

  11. Surgical Results of Lumbar Interbody Fusion Using Calcium Phosphate Cement

    OpenAIRE

    HIRASAWA, Motohiro; Mure, Hideo; Toi, Hiroyuki; Nagahiro, Shinji

    2014-01-01

    Clinical and radiological outcomes of lumbar interbody fusion using artificial fusion cages filled with calcium phosphate cements (CPCs) were retrospectively reviewed. Between 2002 and 2011, 25 patients underwent lumbar interbody fusion at Tokushima University Hospital, and 22 patients were enrolled in this study. Of these, 5 patients received autologous local bone grafts and 17 received CPC. Japan Orthopedic Association (JOA) score was used for clinical outcome assessments. Lumbar radiograph...

  12. Calcium Sulfoaluminate Eco-Cement from Industrial Waste

    OpenAIRE

    Ukrainczyk, N.; Frankoviæ Mihelj, N.; Šipušić, J.

    2013-01-01

    In this paper, the potential benefits offered by calcium sulfoaluminate cement (CSA) production from industrial wastes or by-products already present in Republic of Croatia have been addressed. A variety of industrial wastes, namely phosphogypsum (PG), coal bottom ash (BA) and electric arc furnace slag (EAFS) were used as raw materials to provide additional environmental advantages in production of CSA. Mass fraction of Ye’elimite, the principal hydraulic mineral in the prepared CSA was de...

  13. Furcal perforation repair using calcium enriched mixture cement

    OpenAIRE

    Asgary Saeed

    2010-01-01

    This case describes a furcal perforation in a mandibular first molar accompanied by furcal lesion which has been managed after one month. Root canal treatment was performed; subsequently, the defect was repaired with calcium enriched mixture (CEM) cement. The endodontically treated tooth was restored with amalgam. A 24-month recall showed no evidence of periodontal breakdown, no symptoms, in addition to completes healing of furcal lesion. According to physical and biological properties of the...

  14. Calcium Aluminate based Cement as Dental Restorative Materials

    OpenAIRE

    Kraft, Lars

    2002-01-01

    This thesis presents the results from the development process of a ceramic dental filling material based on calcium aluminate cement. The main focus of the work concerns dimensional changes during setting, hardening and curing and the understanding of the factors controlling the dimensional stability of the system. A range of compositions for research purposes and the composition of Doxadent™ – a dental product launched on the Swedish market in October 2000 – were evaluated. Furthermore hardn...

  15. Sealing of cracks in cement using microencapsulated sodium silicate

    OpenAIRE

    Giannaros, Petros; Kanellopoulos, Antonios; Al-Tabbaa, Abir

    2016-01-01

    Cement-based materials possess inherent autogenous self-healing capability allowing them to seal, and potentially heal, microcracks. This can be improved through the addition of microencapsulated healing agents for autonomic self-healing. The fundamental principle of this self-healing mechanism is that when cracks propagate in the cementitious matrix, they rupture the dispersed capsules and their content (cargo material) is released into the crack volume. Various healing agents have been expl...

  16. Prediction of the Setting Properties of Calcium Phosphate Bone Cement

    Directory of Open Access Journals (Sweden)

    Seyed Mahmud Rabiee

    2012-01-01

    Full Text Available Setting properties of bone substitutes are improved using an injectable system. The injectable bone graft substitutes can be molded to the shape of the bone cavity and set in situ when injected. Such system is useful for surgical operation. The powder part of the injectable bone cement is included of β-tricalcium phosphate, calcium carbonate, and dicalcium phosphate and the liquid part contains poly ethylene glycol solution with different concentrations. In this way, prediction of the mechanical properties, setting times, and injectability helps to optimize the calcium phosphate bone cement properties. The objective of this study is development of three different adaptive neurofuzzy inference systems (ANFISs for estimation of compression strength, setting time, and injectability using the data generated based on experimental observations. The input parameters of models are polyethylene glycol percent and liquid/powder ratio. Comparison of the predicted values and measured data indicates that the ANFIS model has an acceptable performance to the estimation of calcium phosphate bone cement properties.

  17. Prediction of the setting properties of calcium phosphate bone cement.

    Science.gov (United States)

    Rabiee, Seyed Mahmud; Baseri, Hamid

    2012-01-01

    Setting properties of bone substitutes are improved using an injectable system. The injectable bone graft substitutes can be molded to the shape of the bone cavity and set in situ when injected. Such system is useful for surgical operation. The powder part of the injectable bone cement is included of β-tricalcium phosphate, calcium carbonate, and dicalcium phosphate and the liquid part contains poly ethylene glycol solution with different concentrations. In this way, prediction of the mechanical properties, setting times, and injectability helps to optimize the calcium phosphate bone cement properties. The objective of this study is development of three different adaptive neurofuzzy inference systems (ANFISs) for estimation of compression strength, setting time, and injectability using the data generated based on experimental observations. The input parameters of models are polyethylene glycol percent and liquid/powder ratio. Comparison of the predicted values and measured data indicates that the ANFIS model has an acceptable performance to the estimation of calcium phosphate bone cement properties. PMID:22919372

  18. Preparation, characterization and cytocompatibility of bioactive coatings on porous calcium-silicate-hydrate scaffolds

    International Nuclear Information System (INIS)

    The major goal of this research was to investigate and characterize the deposition of a biomimetic apatite-like coating onto the surface of 3D porous calcium-silicate-hydrate scaffolds with suitable bioactivity for potential application in bone tissue engineering. Basically, Portland cement, water, sand and lime were mixed for preparing the slurry which was poured into molds, and fine aluminum powder was added as foaming agent resulting on the formation of porous 3D structures. After aging for 28 days, these porous inorganic scaffolds were immersed in calcium chloride supersaturated solution in PBS for 7 days at 37 deg. C for the biomimetic layer deposition. Scanning electron microscopy (SEM), X-ray diffraction (XRD) and Fourier Transformed Infrared Spectroscopy (FTIR) techniques were used in order to characterize the porous scaffolds and the apatite-like biomimetic coating. The results have showed that 3D constructs were successfully produced with interconnected porosity, compressive strength and cytocompatibility appropriate for potential use as an alternative in trabecular bone repair.

  19. Effect of temperature and aluminium on calcium (alumino)silicate hydrate chemistry under equilibrium conditions

    International Nuclear Information System (INIS)

    There exists limited information regarding the effect of temperature on the structure and solubility of calcium aluminosilicate hydrate (C–A–S–H). Here, calcium (alumino)silicate hydrate (C–(A–)S–H) is synthesised at Ca/Si = 1, Al/Si ≤ 0.15 and equilibrated at 7–80 °C. These systems increase in phase-purity, long-range order, and degree of polymerisation of C–(A–)S–H chains at higher temperatures; the most highly polymerised, crystalline and cross-linked C–(A–)S–H product is formed at Al/Si = 0.1 and 80 °C. Solubility products for C–(A–)S–H were calculated via determination of the solid-phase compositions and measurements of the concentrations of dissolved species in contact with the solid products, and show that the solubilities of C–(A–)S–H change slightly, within the experimental uncertainty, as a function of Al/Si ratio and temperature between 7 °C and 80 °C. These results are important in the development of thermodynamic models for C–(A–)S–H to enable accurate thermodynamic modelling of cement-based materials

  20. Biocompatibility and bioactivity of calcium silicate-based endodontic sealers in human dental pulp cells

    OpenAIRE

    Leticia Boldrin MESTIERI; GOMES-CORNÉLIO, Ana Lívia; RODRIGUES, Elisandra Márcia; SALLES, Loise Pedrosa; BOSSO-MARTELO, Roberta; Juliane Maria GUERREIRO-TANOMARU; TANOMARU-FILHO, Mário

    2015-01-01

    Mineral Trioxide Aggregate (MTA) is a calcium silicate-based material. New sealers have been developed based on calcium silicate as MTA Fillapex and MTA Plus. Objective The aim of this study was to evaluate biocompatibility and bioactivity of these two calcium silicate-based sealers in culture of human dental pulp cells (hDPCs). Material and Methods The cells were isolated from third molars extracted from a 16-year-old patient. Pulp tissue was sectioned into fragments with approximately 1 mm3...

  1. LABORATORY INVESTIGATIONS OF SILICATE MUD CONTAMINATION WITH CALCIUM

    OpenAIRE

    Nediljka Gaurina-Međimurec; Katarina Simon; Davorin Matanović

    2004-01-01

    The silicate-based drilling fluid is a low solids KCl/polymer system with the addition of soluble sodium or potassium silicate to enhance inhibition and wellbore stability. Silicate-based drilling fluids exhibit remarkable shale and chalk stabilizing properties, resulting in gauge hole and the formation of firm cuttings when drilling reactive shales and soft chalks. Silicates protect shales by in-situ gellation when exposed to the neutral pore fluid and precipitation, which occurs on contact ...

  2. Preparation of calcium silicate absorbent from iron blast furnace slag.

    Science.gov (United States)

    Brodnax, L F; Rochelle, G T

    2000-09-01

    Calcium silicate hydrate (CSH) solids were prepared from hydrated lime and iron blast furnace slag in an aqueous agitated slurry at 92 degrees C. While it was hoped a minimal lime/slag ratio could be used to create near-amorphous CSH, the surface area of the product improved by increasing the lime/slag weight ratio to 2. The addition of gypsum to the lime/slag system dramatically improved the formation of surface area, creating solids with 139 m2/g after 30 hr of reaction when only a minimal amount of lime was present. The SO2 reactivity of solids prepared with gypsum greatly exceeded that of hydrated lime, achieving greater than 70-80% conversion of the alkalinity after 1 hr of reaction with SO2. The use of CaCl2 as an additive to the lime/slag system, in lieu of gypsum, also produced high-surface-area solids, 115 m2/g after 21 hr of reaction. However, the SO2 reactivity of these sorbents was relatively low given the high surface area. This emphasized that the correlation between surface area and SO2 reactivity was highly dependent on the solid phase, which was subsequently dependent on slurry composition. PMID:11055162

  3. Biocompatibility of a new nanomaterial based on calcium silicate implanted in subcutaneous connective tissue of rats

    OpenAIRE

    Petrović Violeta; Opačić-Galić Vanja; Jokanović V.; Jovanović M.; Basta-Jovanović Gordana; Živković S.

    2012-01-01

    The aim of the study was to investigate rat connective tissue response to a new calcium silicate system 7, 15, 30 and 60 days after implantation. Twenty Wistar albino male rats received two tubes half-filled with a new calcium silicate system (NCSS) or MTA in subcutaneous tissue. The empty half of the tubes served as controls. Five animals were sacrificed after 7, 15, 30 and 60 days and samples of the subcutaneous tissue around implanted material were submi...

  4. Determine the Compressive Strength of Calcium Silicate Bricks by Combined Nondestructive Method

    OpenAIRE

    2014-01-01

    The paper deals with the application of combined nondestructive method for assessment of compressive strength of calcium silicate bricks. In this case, it is a combination of the rebound hammer method and ultrasonic pulse method. Calibration relationships for determining compressive strength of calcium silicate bricks obtained from nondestructive parameter testing for the combined method as well as for the L-type Schmidt rebound hammer and ultrasonic pulse method are quoted here. Calibration ...

  5. Influence of portland cement replacement in high calcium fly ash geopolymer paste

    Directory of Open Access Journals (Sweden)

    Tanakorn Phoo-ngernkham

    2014-03-01

    Full Text Available This article presents the influence of ordinary Portland cement (OPC replacement in high calcium fly ash (FA geopolymer paste. FA was used to replace OPC at the rate of 5, 10 and 15% by mass of binder. Sodium silicate (Na2SiO3 and 10 molar sodium hydroxide (NaOH solutions were used as the alkaline solution in the reaction. The Na2SiO3/NaOH ratio of 2.0 and the liquid/binder (L/B ratio of 0.60 were used in all mixtures. The results of increase OPC replacement, the setting time and compressive strain capacity decreased while the compressive strength and modulus of elasticity increased. The compressive strength and modulus of elasticity at 28 days of geopolymer pastes with 15% OPC replacement were 36.7 MPa and 13,300 MPa, respectively.

  6. Hydration characteristics and environmental friendly performance of a cementitious material composed of calcium silicate slag.

    Science.gov (United States)

    Zhang, Na; Li, Hongxu; Zhao, Yazhao; Liu, Xiaoming

    2016-04-01

    Calcium silicate slag is an alkali leaching waste generated during the process of extracting Al2O3 from high-alumina fly ash. In this research, a cementitious material composed of calcium silicate slag was developed, and its mechanical and physical properties, hydration characteristics and environmental friendly performance were investigated. The results show that an optimal design for the cementitious material composed of calcium silicate slag was determined by the specimen CFSC7 containing 30% calcium silicate slag, 5% high-alumina fly ash, 24% blast furnace slag, 35% clinker and 6% FGD gypsum. This blended system yields excellent physical and mechanical properties, confirming the usefulness of CFSC7. The hydration products of CFSC7 are mostly amorphous C-A-S-H gel, rod-like ettringite and hexagonal-sheet Ca(OH)2 with small amount of zeolite-like minerals such as CaAl2Si2O8·4H2O and Na2Al2Si2O8·H2O. As the predominant hydration products, rod-like ettringite and amorphous C-A-S-H gel play a positive role in promoting densification of the paste structure, resulting in strength development of CFSC7 in the early hydration process. The leaching toxicity and radioactivity tests results indicate that the developed cementitious material composed of calcium silicate slag is environmentally acceptable. This study points out a promising direction for the proper utilization of calcium silicate slag in large quantities. PMID:26691955

  7. Aqueous deposition of calcium phosphates and silicate substituted calcium phosphates on magnesium alloys

    International Nuclear Information System (INIS)

    Attempts were made to deposit homogeneous films of calcium phosphates (CaPs) on two magnesium alloy systems, AZ31 and Mg–4Y, through an aqueous phosphating bath method. The deposition of silicate substituted CaPs by this aqueous method was also explored as silicate substitution is believed to increase the bioactivity of CaPs. The effect of doped and undoped coatings on the in vitro degradation and bioactivity of both alloy systems was studied. FTIR and EDX confirmed the deposition of Ca, P, and Si on both alloys and the coatings appeared to consist primarily biphasic mixtures of hydroxyapatite and β-TCP. These largely inhomogeneous coatings, as observed by SEM, were not shown to have any significant effect on maintaining the physiological pH of the culture medium in comparison to the uncoated samples, as the pH remained approximately in the 8.4–8.7 range. Interestingly, despite similar pH profiles between the coated and uncoated samples, CaP coatings affected the degradation of both alloys. These doped and undoped calcium phosphate coatings were observed to decrease the degradation of AZ31 whereas they increased the degradation of Mg–4Y. In vitro studies on cell attachment using MC3T3-E1 mouse osteoblasts showed that between the uncoated alloys, Mg–4Y appeared to be the more biocompatible of the two. Silicate substituted CaP coatings were observed to increase the cell attachment on AZ31 compared to bare and undoped CaPs coated samples, but did not have as great of an effect on increasing cell attachment on Mg–4Y.

  8. Understanding silicate hydration from quantitative analyses of hydrating tricalcium silicates

    OpenAIRE

    Pustovgar, Elizaveta; Sangodkar, Rahul P.; Andreev, Andrey S.; Palacios, Marta; Chmelka, Bradley F.; Robert J. Flatt; D'Espinose De Lacaillerie, Jean-Baptiste

    2016-01-01

    Silicate hydration is prevalent in natural and technological processes, such as, mineral weathering, glass alteration, zeolite syntheses and cement hydration. Tricalcium silicate (Ca3SiO5), the main constituent of Portland cement, is amongst the most reactive silicates in water. Despite its widespread industrial use, the reaction of Ca3SiO5 with water to form calcium-silicate-hydrates (C-S-H) still hosts many open questions. Here, we show that solid-state nuclear magnetic resonance measuremen...

  9. New developments in calcium phosphate bone cements: approaching spinal applications

    OpenAIRE

    Vlad, Maria Daniela

    2009-01-01

    La presente tesis doctoral (i.e., “New developments in calcium phosphate bone cements: approaching spinal applications”) aporta nuevos conocimientos en el campo de los cementos óseos de fosfato de calcio (CPBCs) en relación a su aplicación clínica en el campo de la cirugía vertebral mínimamente invasiva. La hipótesis central de esta investigación fue formulada en los siguientes términos: “Los cementos apatíticos pueden ser (si se optimizan) una alternativa mejor (debido a sus propiedades d...

  10. The flame photometric determination of calcium in phosphate, carbonate, and silicate rocks

    Science.gov (United States)

    Kramer, H.

    1957-01-01

    A flame photometric method of determining calcium in phosphate, carbonate, and silicate locks has been developed Aluminum and phosphate interference was overcome by the addition of a large excess of magnesium. The method is rapid and suitable for routine analysis Results obtained are within ?? 2% of the calcium oxide content. ?? 1957.

  11. Interaction grand potential between calcium-silicate-hydrate nanoparticles at the molecular level.

    Science.gov (United States)

    Bonnaud, Patrick A; Labbez, Christophe; Miura, Ryuji; Suzuki, Ai; Miyamoto, Naoto; Hatakeyama, Nozomu; Miyamoto, Akira; Van Vliet, Krystyn J

    2016-02-21

    Calcium-silicate-hydrate (or C-S-H), an inosilicate, is the major binding phase in cement pastes and concretes and a porous hydrated material made up of a percolated and dense network of crystalline nanoparticles of a mean apparent spherical diameter of ∼5 nm that are each stacks of multiple C-S-H layers. Interaction forces between these nanoparticles are at the origin of C-S-H chemical, physical, and mechanical properties at the meso- and macroscales. These particle interactions and the resulting properties may be affected significantly by nanoparticle density and environmental conditions such as the temperature, relative humidity, or concentration of chemical species in the bulk solution. In this study, we combined grand canonical Monte Carlo simulations and an extension of the mean force integration method to derive the pair potentials. This approach enables realistic simulation of the physical environment surrounding the C-S-H particles. We thus constructed the pair potentials for C-S-H nanoparticles of defined chemical stoichiometry at 10% relative humidity (RH), varying the relative crystallographic orientations at a constant particle density of ρpart ∼ 2.21 mmol L(-1). We found that cohesion between nanoparticles is affected strongly by both the aspect ratio and the crystallographic misorientation of interacting particles. This method and the findings underscore the importance of accounting for relative dimensions and orientation among C-S-H nanoparticles in descriptions of physical and simulated multiparticle aggregates or mesoscale systems. PMID:26866999

  12. Reactions of fly ash with calcium aluminate cement and calcium sulphate

    OpenAIRE

    Fernández Carrasco, Lucía; Vázquez Ramonich, Enric

    2009-01-01

    The hydration processes in the ternary system fly ash/calcium aluminate cement/calcium sulphate (FA/CAC/C$) at 20 °C were investigated; six compositions from the ternary system FA/CAC/C$ were selected for this study. The nature of the reaction products in these pastes were analysed by X-ray diffraction (XRD) and infrared spectroscopy (FTIR). At four days reaction time, the main hydration reaction product in these pastes was ettringite and the samples with major initial CAC presented minor ett...

  13. Another look at the deterioration of calcium aluminate cement concrete

    Directory of Open Access Journals (Sweden)

    Jambor, Jaromir

    1996-03-01

    Full Text Available Potential degradation of concrete structures made of calcium aluminate cement (CAC is well known and is caused by transformation (conversion of the thermodynamically metastable into stable calcium aluminate hydrate phases. This recrystallization is influenced by temperature and humidity; the structural degradation of the concrete itself thus its loss of strength, is strongly related to the pore structure of the hydrated cement paste, the critical parameters being the total volume of pores below 15-20 nm and the median micropore radius. This constitutes a novel procedure for evaluation of existing CAC concrete structure.

    La degradación potencial de estructuras de hormigón elaboradas con cemento aluminoso (CA es bien conocida. Este deterioro está causado por la recristalización (conversión de las fases del aluminato cálcico que son termodinámicamente metastables, en fases estables. En esta recristalización influye la temperatura y la humedad. Tanto la degradación del propio hormigón, como su pérdida de resistencias están relacionadas estrechamente con la estructura porosa de la pasta del cemento hidratado, siendo parámetros críticos el volumen total de los poros inferiores a 15-20 nm y el tamaño medio de los radios de los microporos. Esto constituye un nuevo procedimiento para evaluar las estructuras existentes de hormigón de cemento aluminoso (CA.

  14. Evaluation of a porosity measurement method for wet calcium phosphate cements.

    Science.gov (United States)

    Ajaxon, Ingrid; Maazouz, Yassine; Ginebra, Maria-Pau; Öhman, Caroline; Persson, Cecilia

    2015-11-01

    The porosity of a calcium phosphate cement is a key parameter as it affects several important properties of the cement. However, a successful, non-destructive porosity measurement method that does not include drying has not yet been reported for calcium phosphate cements. The aim of this study was to evaluate isopropanol solvent exchange as such a method. Two different types of calcium phosphate cements were used, one basic (hydroxyapatite) and one acidic (brushite). The cements were allowed to set in an aqueous environment and then immersed in isopropanol and stored under three different conditions: at room temperature, at room temperature under vacuum (300 mbar) or at 37℃. The specimen mass was monitored regularly. Solvent exchange took much longer time to reach steady state in hydroxyapatite cements compared to brushite cements, 350 and 18 h, respectively. Furthermore, the immersion affected the quasi-static compressive strength of the hydroxyapatite cements. However, the strength and phase composition of the brushite cements were not affected by isopropanol immersion, suggesting that isopropanol solvent exchange can be used for brushite calcium phosphate cements. The main advantages with this method are that it is non-destructive, fast, easy and the porosity can be evaluated while the cements remain wet, allowing for further analysis on the same specimen. PMID:26163278

  15. Development and characterisation of injectable calcium phosphate cements for use in vertebroplasty

    OpenAIRE

    Pittet, Christian; Lemaître, Jacques

    2007-01-01

    The global objective of this thesis was to understand how the starting components of brushite cements influence the cement properties relevant for its use in vertebroplasty. Therefore, this work focussed on the following cement properties : mechanical strength, X-ray opacity and heat release upon setting. To carry out the global objective, a test protocol was first developed to characterise the mechanical properties of calcium phosphate cements. The Mohr's circles representation allowed to un...

  16. Development and characterisation of injectable calcium phosphate cements for use in vertebroplasty

    OpenAIRE

    Pittet, Christian

    2002-01-01

    The global objective of this thesis was to understand how the starting components of brushite cements influence the cement properties relevant for its use in vertebroplasty. Therefore, this work focussed on the following cement properties : mechanical strength, X-ray opacity and heat release upon setting. To carry out the global objective, a test protocol was first developed to characterise the mechanical properties of calcium phosphate cements. The Mohr's circles representation allowed to un...

  17. Silicate species of water glass and insights for alkali-activated green cement

    Science.gov (United States)

    Jansson, Helén; Bernin, Diana; Ramser, Kerstin

    2015-06-01

    Despite that sodium silicate solutions of high pH are commonly used in industrial applications, most investigations are focused on low to medium values of pH. Therefore we have investigated such solutions in a broad modulus range and up to high pH values (˜14) by use of infrared (IR) spectroscopy and silicon nuclear magnetic resonance (29Si-NMR). The results show that the modulus dependent pH value leads to more or less charged species, which affects the configurations of the silicate units. This in turn, influences the alkali-activation process of low CO2 footprint cements, i.e. materials based on industrial waste or by-products.

  18. Silicate species of water glass and insights for alkali-activated green cement

    Directory of Open Access Journals (Sweden)

    Helén Jansson

    2015-06-01

    Full Text Available Despite that sodium silicate solutions of high pH are commonly used in industrial applications, most investigations are focused on low to medium values of pH. Therefore we have investigated such solutions in a broad modulus range and up to high pH values (∼14 by use of infrared (IR spectroscopy and silicon nuclear magnetic resonance (29Si-NMR. The results show that the modulus dependent pH value leads to more or less charged species, which affects the configurations of the silicate units. This in turn, influences the alkali-activation process of low CO2 footprint cements, i.e. materials based on industrial waste or by-products.

  19. Silicate species of water glass and insights for alkali-activated green cement

    International Nuclear Information System (INIS)

    Despite that sodium silicate solutions of high pH are commonly used in industrial applications, most investigations are focused on low to medium values of pH. Therefore we have investigated such solutions in a broad modulus range and up to high pH values (∼14) by use of infrared (IR) spectroscopy and silicon nuclear magnetic resonance (29Si-NMR). The results show that the modulus dependent pH value leads to more or less charged species, which affects the configurations of the silicate units. This in turn, influences the alkali-activation process of low CO2 footprint cements, i.e. materials based on industrial waste or by-products

  20. Study of cements silicate phases hydrated under high pressure and high temperature; Etude des phases silicatees du ciment hydrate sous haute pression et haute temperature

    Energy Technology Data Exchange (ETDEWEB)

    Meducin, F.

    2001-10-01

    This study concerns the durability of oil-well cementing. Indeed, in oil well cementing a cement slurry is pumped down the steel casing of the well up the annular space between it and the surrounding rock to support and protect the casing. The setting conditions of pressure and temperature may be very high (up to 1000 bar and 250 deg C at the bottom of the oil-well). In this research, the hydration of the main constituent of cement, synthetic tri-calcium silicate Ca{sub 3}SiO{sub 2}, often called C{sub 3}S (C = CaO; S = SiO{sub 2} and H H{sub 2}O), is studied. Calcium Silicate hydrates are prepared in high-pressure cells to complete their phase diagram (P,T) and obtain the stability conditions for each species. Indeed, the phases formed in these conditions are unknown and the study consists in the hydration of C{sub 3}S at different temperatures, pressures, and during different times to simulate the oil-well conditions. In a first step (until 120 deg C at ambient pressure) the C-S-H, a not well crystallized and non-stoichiometric phase, is synthesized: it brings adhesion and mechanical properties., Then, when pressure and temperature increase, crystallized phases appear such as jaffeite (Ca{sub 6}(Si{sub 2}O{sub 7})(OH){sub 6}) and hillebrandite (Ca{sub 2}(SiO{sub 3})(OH){sub 2}). Silicon {sup 29}Si Nuclear Magnetic Resonance (using standard sequences MAS, CPMAS) allow us to identify all the silicates hydrates formed. Indeed, {sup 29}Si NMR is a valuable tool to determine the structure of crystallized or not-well crystallized phases of cement. The characterization of the hydrated samples is completed by other techniques: X- Ray Diffraction and Scanning Electron Microscopy. The following results are found: jaffeite is the most stable phase at C/S=3. To simulate the hydration of real cement, hydration of C{sub 3}S with ground quartz and with or without super-plasticizers is done. In those cases, new phases appear: kilchoanite mainly, and xonotlite. A large amount of

  1. Optimization of calcium chloride content on bioactivity and mechanical properties of white Portland cement

    International Nuclear Information System (INIS)

    This research investigates the optimization of calcium chloride content on the bioactivity and mechanical properties of white Portland cement. Calcium chloride was used as an addition of White Portland cement at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9 and 10% by weight. Calcium chloride was dissolved in sterile distilled water and blended with White Portland cement using a water to cement ratio of 0.5. Analysis of the bioactivity and pH of white Portland cement pastes with calcium chloride added at various amounts was carried out in simulated body fluid. Setting time, density, compressive strength and volume of permeable voids were also investigated. The characteristics of cement pastes were examined by X-ray diffractometer and scanning electron microscope linked to an energy-dispersive X-ray analyzer. The result indicated that the addition of calcium chloride could accelerate the hydration of white Portland cement, resulting in a decrease in setting time and an increase in early strength of the pastes. The compressive strength of all cement pastes with added calcium chloride was higher than that of the pure cement paste, and the addition of calcium chloride at 8 wt.% led to achieving the highest strength. Furthermore, white Portland cement pastes both with and without calcium chloride showed well-established bioactivity with respect to the formation of a hydroxyapatite layer on the material within 7 days following immersion in simulated body fluid; white Portland cement paste with added 3%CaCl2 exhibited the best bioactivity. - Highlights: ► Optimization CaCl2 content on the bioactivity and mechanical properties. ► CaCl2 was used as an addition at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9 and 10% by weight. ► CaCl2 resulted in a decrease in setting time and an increase in early strength. ► Addition of 3%CaCl2 exhibited the optimum formation of hydroxyapatite.

  2. Sorption of caesium and strontium onto calcium silicate hydrate in saline groundwater

    International Nuclear Information System (INIS)

    Full text of publication follows: In the concept for radioactive waste disposal in Japan, cement is a potential waste packaging and backfilling material and is expected to provide chemical containment. The sorption of radionuclides onto cement materials, which controls the aqueous concentrations of elements in the pore-water, is a very important parameter when considering the release of radionuclides from the near field of a cementitious radioactive waste repository. Many safety assessment calculations currently assume radionuclide retardation as linear sorption equilibrium and describe it with a distribution ratio (Rd value). In this study, the sorption mechanism is discussed by measuring the sorption isotherm of caesium, strontium (10-5 ∼ 10-2 mol dm-3) and sodium (10-4 ∼ 10-1 mol dm-3) onto Calcium Silicate Hydrate (C-S-H gel, Ca/Si 0.65 ∼ 1.2) at a liquid:solid ratio of 100:1, to support the assumption. In addition, the competitive sorption between caesium or strontium, and sodium is studied by sorption measurements using a range of sodium chloride concentration to simulate different ionic strengths in saline groundwater. The initial and equilibrated aqueous compositions were measured in the sorption experiments and it was found that caesium, strontium and sodium were sorbed by substitution for Ca in C-S-H phases by examining the mass balance. Based on the experimental results, we propose a modelling approach in which the ion-exchange model is employed and the presence of some calcium sites with different ion-exchange log K values in C-S-H is assumed by considering the composition and the structure of C-S-H. The modelling calculation results predict the measured Rd values well and also describe the competition of sorption of caesium or strontium, and sodium in the experiments. The log K values for sorption of each cation element decreased as Ca/Si ratio of C-S-H gel increased. This agrees with the trend that C-S-H gel is negatively charged at low Ca

  3. Creating of highly active calcium-silicate phases for application in endodontics

    OpenAIRE

    Čolović B.; Jokanović V.; Jović N.

    2013-01-01

    The synthesis of active silicate phases by combined sol gel and high-temperature selfpropagating wave method, is described in this paper. They show a significant decrease of setting time and good mechanical properties, which are very important for its potential application in endodontic practice. Particularly, process of hydration of calcium silicate phases is carefully analyzed, from the aspect of phase changes during their soaking in water for 1, 3, 7 and...

  4. Kinetics and Mechanism of Adsorption of Phosphate on Fluorine-containing Calcium Silicate

    Institute of Scientific and Technical Information of China (English)

    ZHU Xinhua; ZHANG Zhao; SHEN Jun

    2016-01-01

    The nanowires-reticulated calcium silicate with a speciifc surface area more than 100 m2/g was prepared by a hydrothermal process using hydrated lime (Ca(OH)2, HL) and silica containing soluble lfuoride, which was a by-product of lfuorine industry, and the soluble lfuoride in raw silica was ifxed as CaSiF6 at the same time. The kinetic characteristics and mechanism of adsorbing phosphate by lfuorine-containing calcium silicate were investigated in the experiments of phosphorus (P) removal from aqueous solution. The results show that the prepared lfuorine-containing calcium silicate has excellent performance for adsorbing phosphate, the adsorption process appears to follow pseudo-second-order reaction kinetics and the process is mainly controlled by chemisorption. The product resulted from P adsorption is mainly composed of hydroxyapatite (HAP) and lfuorapatite (FAP), which are further used as adsorbents of heavy metal ion Cd2+ in aqueous solution and display excellent performance.

  5. Augmentation of Pedicle Screw Fixation with Calcium Phosphate Cement

    Institute of Scientific and Technical Information of China (English)

    YANG Shu-hua; FU De-hao; LI Jin; XU Wei-hua; YANG Cao; YE Zhe-wei; ZUO Xiao-yan

    2004-01-01

    To determine whether a biodegradable calcium phosphate cement(CPC) provides significant augmentation of pedicle screw fixation or not,an in vitro biomechanical study was carried out to evaluate the biomechanical effect of CPC in the restoration and augmentation of pedicle screw fixation.Axial pullout test and cyclic bending resistance test were employed in the experiment,and polymethylmethacrylate (PMMA) was chosen as control.The results demonstrate that the pullout strengths following CPC restoration and augmentation are 74% greater on an average than those of the control group,but less than those of PMMA restoration group and augmentation group respectively (increased by 126% versus control).In cyclic bending resistance test,the CPC augmented screws are found to withstand a greater number of cycles or greater loading with less displacement before loosening,but the augmentation effect of PMMA is greater than that of CPC.

  6. The bactericidal and biocompatible characteristics of reinforced calcium phosphate cements

    International Nuclear Information System (INIS)

    Infection remains a serious medical problem in orthopaedic surgery. Antibiotic administration can be available either systemically via the blood stream or locally, directly into the infected bone. One of the main limitations of antibiotic administration is the development of multi-antibiotic-resistant bacterial strains. In this study, we developed bactericidal calcium phosphate cements (CPC) by incorporation of different molecular weight chitosan and hydroxypropyltrimethyl ammonium chloride chitosan (HACC). Two standard strains, S. epidermidis (ATCC35984) and S. aureus (ATCC25923), and one clinical isolate, methicillin-resistant S. epidermidis (MRSE), were selected to evaluate the antibacterial activity of these bone cements. Our data showed that the CPC loaded with low molecular weight chitosan and HACC significantly inhibited the bacterial adhesion and biofilm formation. In addition, HACC-containing CPC has no cytotoxic effects on both mouse pluripotent C3H10T1/2cell line and a murine L929 fibroblast cell line. We propose that HACC-containing CPC represents a promising polymer-based bactericidal bone scaffold in controlling orthopaedic surgery-related infection. (paper)

  7. Hydration studies of calcium sulfoaluminate cements blended with fly ash

    International Nuclear Information System (INIS)

    The main objective of this work is to study the hydration and properties of calcium sulfoaluminate cement pastes blended with fly ash (FA) and the corresponding mortars at different hydration ages. Laboratory X-ray powder diffraction, rheological studies, thermal analysis, porosimetry and compressive strength measurements were performed. The analysis of the diffraction data by Rietveld method allowed quantifying crystalline phases and overall amorphous contents. The studied parameters were: i) FA content, 0, 15 and 30 wt.%; and ii) water addition, water-to-CSA mass ratio (w/CSA = 0.50 and 0.65), and water-to-binder mass ratio (w/b = 0.50). Finally, compressive strengths after 6 months of 0 and 15 wt.% FA [w/CSA = 0.50] mortars were similar: 73 ± 2 and 72 ± 3 MPa, respectively. This is justified by the filler effect of the FA as no strong evidences of reactivity of FA with CSA were observed. These results support the partial substitution of CSA cements with FA with the economic and environmental benefits

  8. Hydration studies of calcium sulfoaluminate cements blended with fly ash

    Energy Technology Data Exchange (ETDEWEB)

    García-Maté, M.; De la Torre, A.G. [Departamento de Química Inorgánica, Cristalografía y Mineralogía, Universidad de Málaga, 29071 Málaga (Spain); León-Reina, L. [Servicios Centrales de Apoyo a la Investigación, Universidad de Málaga, 29071 Málaga (Spain); Aranda, M.A.G. [Departamento de Química Inorgánica, Cristalografía y Mineralogía, Universidad de Málaga, 29071 Málaga (Spain); CELLS-Alba synchrotron, Carretera BP 1413, Km. 3.3, E-08290 Cerdanyola, Barcelona (Spain); Santacruz, I., E-mail: isantacruz@uma.es [Departamento de Química Inorgánica, Cristalografía y Mineralogía, Universidad de Málaga, 29071 Málaga (Spain)

    2013-12-15

    The main objective of this work is to study the hydration and properties of calcium sulfoaluminate cement pastes blended with fly ash (FA) and the corresponding mortars at different hydration ages. Laboratory X-ray powder diffraction, rheological studies, thermal analysis, porosimetry and compressive strength measurements were performed. The analysis of the diffraction data by Rietveld method allowed quantifying crystalline phases and overall amorphous contents. The studied parameters were: i) FA content, 0, 15 and 30 wt.%; and ii) water addition, water-to-CSA mass ratio (w/CSA = 0.50 and 0.65), and water-to-binder mass ratio (w/b = 0.50). Finally, compressive strengths after 6 months of 0 and 15 wt.% FA [w/CSA = 0.50] mortars were similar: 73 ± 2 and 72 ± 3 MPa, respectively. This is justified by the filler effect of the FA as no strong evidences of reactivity of FA with CSA were observed. These results support the partial substitution of CSA cements with FA with the economic and environmental benefits.

  9. Synthesis optimization of calcium aluminate cement phases for biomedical applications

    International Nuclear Information System (INIS)

    Calcium aluminate cement (CAC) has been studied as a potential material for applications in the areas of health such as, endodontics and bone reconstruction. These studies have been based on commercial products consisting of a mixture of phases. Improvements can be attained by investigating the synthesis routes of CAC aiming the proper balance between the phases and the control of impurities that may impair its performance for biomedical applications. Thus, the aim of this work was to study the CAC synthesis routes in the Al2O3-CaCO3 and Al2O3-CaO systems, as well as the phase characterization attained by means of X ray analysis. The Al2O3-CaO route enabled the production of the target phases (CA, CA2, C3A and C12A7) with a higher purity compared to the Al2O3-CaCO3 one. As a result the particular properties of these phases can be evaluated to define a more suitable composition that results in better properties for an endodontic cement and other applications. (author)

  10. Alleviating aluminum toxicity in an acid sulfate soil from Peninsular Malaysia by calcium silicate application

    Science.gov (United States)

    Elisa, A. A.; Ninomiya, S.; Shamshuddin, J.; Roslan, I.

    2016-03-01

    In response to human population increase, the utilization of acid sulfate soils for rice cultivation is one option for increasing production. The main problems associated with such soils are their low pH values and their associated high content of exchangeable Al, which could be detrimental to crop growth. The application of soil amendments is one approach for mitigating this problem, and calcium silicate is an alternative soil amendment that could be used. Therefore, the main objective of this study was to ameliorate soil acidity in rice-cropped soil. The secondary objective was to study the effects of calcium silicate amendment on soil acidity, exchangeable Al, exchangeable Ca, and Si content. The soil was treated with 0, 1, 2, and 3 Mg ha-1 of calcium silicate under submerged conditions and the soil treatments were sampled every 30 days throughout an incubation period of 120 days. Application of calcium silicate induced a positive effect on soil pH and exchangeable Al; soil pH increased from 2.9 (initial) to 3.5, while exchangeable Al was reduced from 4.26 (initial) to 0.82 cmolc kg-1. Furthermore, the exchangeable Ca and Si contents increased from 1.68 (initial) to 4.94 cmolc kg-1 and from 21.21 (initial) to 81.71 mg kg-1, respectively. Therefore, it was noted that calcium silicate was effective at alleviating Al toxicity in acid sulfate, rice-cropped soil, yielding values below the critical level of 2 cmolc kg-1. In addition, application of calcium silicate showed an ameliorative effect as it increased soil pH and supplied substantial amounts of Ca and Si.

  11. A Novel Synthesis Method of Porous Calcium Silicate Hydrate Based on the Calcium Oxide/Polyethylene Glycol Composites

    OpenAIRE

    Wei Guan; Fangying Ji; Yong Cheng; Zhuoyao Fang; Dexin Fang; Peng Yan; Qingkong Chen

    2013-01-01

    This paper proposed a novel method to prepare porous calcium silicate hydrate (CSH) based on the calcium oxide/polyethylene glycol (CaO/PEG2000) composites as the calcium materials. The porosity formation mechanism was revealed via X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), Brunauer-Emmett-Teller (BET), and Fourier transformed infrared spectroscopy (FT-IR). The reactivity of silica materials (SiO2) enhanced by increasing pH value. Ca2+ could not sustain rele...

  12. Effects of calcium hydroxide addition on the physical and chemical properties of a calcium silicate-based sealer

    OpenAIRE

    KUGA, Milton Carlos; DUARTE Marco Antonio Hungaro; SANT'ANNA-JÚNIOR, Arnaldo; KEINE, Kátia Cristina; FARIA, Gisele; Andrea Abi Rached DANTAS; GUIOTTI, Flávia Angélica

    2014-01-01

    Recently, various calcium silicate-based sealers have been introduced for use in root canal filling. The MTA Fillapex is one of these sealers, but some of its physicochemical properties are not in accordance with the ISO requirements. Objective: The aim of this study was to evaluate the flowability, pH level and calcium release of pure MTA Fillapex (MTAF) or containing 5% (MTAF5) or 10% (MTAF10) calcium hydroxide (CH), in weight, in comparison with AH Plus sealer. Material and Methods: The...

  13. Effects of Silicate, Phosphate, and Calcium on the Stability of Aldopentoses

    Science.gov (United States)

    Nitta, Sakiko; Furukawa, Yoshihiro; Kakegawa, Takeshi

    2016-06-01

    Ribose is an important constituent of RNA: ribose connects RNA bases and forms a strand of sugar phosphates. Accumulation of ribose on prebiotic Earth was difficult because of its low stability. Improvement in the yield of ribose by the introduction of borate or silicate in a formose-like reaction has been proposed. The effects of borates have been further analyzed and confirmed in subsequent studies. Nonetheless, the effects of silicates and phosphates remain unclear. In the present study, we incubated aldopentoses in a highly alkaline aqueous solution at a moderate temperature to determine the effects of silicate or phosphate on the degradation rates of ribose and its isomeric aldopentoses. The formation of a complex of silicate (or phosphate) with ribose was also analyzed in experiments with 29Si and 31P nuclear magnetic resonance (NMR). We found that silicate or phosphate complexes of ribose were not detectable under our experimental conditions. The stability of ribose and lyxose improved after addition of 40-fold molar excess (relative to a pentose) of sodium silicate or sodium phosphate to the alkaline solution. The stability was not improved further when an 80-fold molar excess of sodium silicate or sodium phosphate was added. Calcium was removed from these solutions by precipitation of calcium salts. The drop in Ca2+ concentration might have improved the stability of ribose and lyxose, which are susceptible to aldol addition. The improvement of ribose stability by the removal of Ca2+ and by addition of silicate or phosphate was far smaller than the improvement by borate. Furthermore, all aldopentoses showed similar stability in silicate- and phosphate-containing solutions. These results clearly show that selective stabilization of ribose by borate cannot be replaced by the effects of silicate or phosphate; this finding points to the importance of borate in prebiotic RNA formation.

  14. Effects of Silicate, Phosphate, and Calcium on the Stability of Aldopentoses.

    Science.gov (United States)

    Nitta, Sakiko; Furukawa, Yoshihiro; Kakegawa, Takeshi

    2016-06-01

    Ribose is an important constituent of RNA: ribose connects RNA bases and forms a strand of sugar phosphates. Accumulation of ribose on prebiotic Earth was difficult because of its low stability. Improvement in the yield of ribose by the introduction of borate or silicate in a formose-like reaction has been proposed. The effects of borates have been further analyzed and confirmed in subsequent studies. Nonetheless, the effects of silicates and phosphates remain unclear. In the present study, we incubated aldopentoses in a highly alkaline aqueous solution at a moderate temperature to determine the effects of silicate or phosphate on the degradation rates of ribose and its isomeric aldopentoses. The formation of a complex of silicate (or phosphate) with ribose was also analyzed in experiments with (29)Si and (31)P nuclear magnetic resonance (NMR). We found that silicate or phosphate complexes of ribose were not detectable under our experimental conditions. The stability of ribose and lyxose improved after addition of 40-fold molar excess (relative to a pentose) of sodium silicate or sodium phosphate to the alkaline solution. The stability was not improved further when an 80-fold molar excess of sodium silicate or sodium phosphate was added. Calcium was removed from these solutions by precipitation of calcium salts. The drop in Ca(2+) concentration might have improved the stability of ribose and lyxose, which are susceptible to aldol addition. The improvement of ribose stability by the removal of Ca(2+) and by addition of silicate or phosphate was far smaller than the improvement by borate. Furthermore, all aldopentoses showed similar stability in silicate- and phosphate-containing solutions. These results clearly show that selective stabilization of ribose by borate cannot be replaced by the effects of silicate or phosphate; this finding points to the importance of borate in prebiotic RNA formation. PMID:26559965

  15. Electrophoretic deposition of calcium silicate-reduced graphene oxide composites on titanium substrate

    DEFF Research Database (Denmark)

    Mehrali, Mehdi; Akhiani, Amir Reza; Talebian, Sepehr;

    2016-01-01

    silicate-reduced graphene oxide (CS-rGO) composites were synthesized, using an in situ hydrothermal method. CS nanowires were uniformly decorated on the rGO, with an appropriate interfacial bonding. The CS-rGO composites behaved like hybrid composites when deposited on a titanium substrate by cathodic......Calcium silicate (CS)/graphene coatings have been used to improve the biological and mechanical fixation of metallic prosthesis. Among the extraordinary features of graphene is its very high mechanical strength, which makes it an attractive nanoreinforcement material for composites. Calcium...

  16. Conservative approach of a symptomatic carious immature permanent tooth using a tricalcium silicate cement (Biodentine): a case report.

    Science.gov (United States)

    Villat, Cyril; Grosgogeat, Brigitte; Seux, Dominique; Farge, Pierre

    2013-11-01

    The restorative management of deep carious lesions and the preservation of pulp vitality of immature teeth present real challenges for dental practitioners. New tricalcium silicate cements are of interest in the treatment of such cases. This case describes the immediate management and the follow-up of an extensive carious lesion on an immature second right mandibular premolar. Following anesthesia and rubber dam isolation, the carious lesion was removed and a partial pulpotomy was performed. After obtaining hemostasis, the exposed pulp was covered with a tricalcium silicate cement (Biodentine, Septodont) and a glass ionomer cement (Fuji IX extra, GC Corp.) restoration was placed over the tricalcium silicate cement. A review appointment was arranged after seven days, where the tooth was asymptomatic with the patient reporting no pain during the intervening period. At both 3 and 6 mon follow up, it was noted that the tooth was vital, with normal responses to thermal tests. Radiographic examination of the tooth indicated dentin-bridge formation in the pulp chamber and the continuous root formation. This case report demonstrates a fast tissue response both at the pulpal and root dentin level. The use of tricalcium silicate cement should be considered as a conservative intervention in the treatment of symptomatic immature teeth. PMID:24303363

  17. Retention capacity of the calcium silicates hydrates (CSH) for caesium

    International Nuclear Information System (INIS)

    Alkalis are poorly trapped by cement and this constitutes one of the problem for the use of cement as nuclear waste matrix. Therefore we have studied the sorption of 137Cs on the CSH which are the major components of a Portland cement. CSH of different Ca/Si has been synthetised in suspension. Caesium chloride, which is highly soluble, was placed in a reactor with the CSH. To have a high precision for the caesium quantity fixed by the CSH, radioactive caesium was used as tracer. We observed that the maximum exchange capacity occurs at low Ca/Si ratio, when the structure is close to that of tobermorite. A Cs/Ca molar ratio around one could be obtained in this structure. (orig.)

  18. Structural characterization of magnesium silicate hydrate: towards the design of eco-sustainable cements.

    Science.gov (United States)

    Tonelli, M; Martini, F; Calucci, L; Fratini, E; Geppi, M; Ridi, F; Borsacchi, S; Baglioni, P

    2016-02-28

    Magnesium-based cement is one of the most interesting eco-sustainable alternatives to standard cementitious binders. The reasons for the interest towards this material are twofold: (i) its production process, using magnesium silicates, brine or seawater, dramatically reduces CO2 emissions with respect to Portland cement production, and (ii) it is very well suited to applications in radioactive waste encapsulation. In spite of its potential, assessment of the structural properties of its binder phase (magnesium silicate hydrate or M-S-H) is far from complete, especially because of its amorphous character. In this work, a comprehensive structural characterization of M-S-H was obtained using a multi-technique approach, including a detailed solid-state NMR investigation and, in particular, for the first time, quantitative (29)Si solid-state NMR data. M-S-H was prepared through room-temperature hydration of highly reactive MgO and silica fume and was monitored for 28 days. The results clearly evidenced the presence in M-S-H of "chrysotile-like" and "talc-like" sub-nanometric domains, which are approximately in a 1 : 1 molar ratio after long-time hydration. Both these kinds of domains have a high degree of condensation, corresponding to the presence of a small amount of silanols in the tetrahedral sheets. The decisive improvement obtained in the knowledge of M-S-H structure paves the way for tailoring the macroscopic properties of eco-sustainable cements by means of a bottom-up approach. PMID:26781557

  19. Effect of temperature on the hydration of Portland cement blended with siliceous fly ash

    International Nuclear Information System (INIS)

    The effect of temperature on the hydration of Portland cement pastes blended with 50 wt.% of siliceous fly ash is investigated within a temperature range of 7 to 80 °C. The elevation of temperature accelerates both the hydration of OPC and fly ash. Due to the enhanced pozzolanic reaction of the fly ash, the change of the composition of the C–S–H and the pore solution towards lower Ca and higher Al and Si concentrations is shifted towards earlier hydration times. Above 50 °C, the reaction of fly ash also contributes to the formation of siliceous hydrogarnet. At 80 °C, ettringite and AFm are destabilised and the released sulphate is partially incorporated into the C–S–H. The observed changes of the phase assemblage in dependence of the temperature are confirmed by thermodynamic modelling. The increasingly heterogeneous microstructure at elevated temperatures shows an increased density of the C–S–H and a higher coarse porosity. -- Highlights: •The reaction of quartz powder at 80 °C strongly enhances the compressive strength. •Almost no strength increase of fly ash blended OPC at 80 °C was found after 2 days. •Siliceous hydrogarnet is formed upon the reaction of fly ash at high temperatures. •Temperature dependent change of the system was simulated by thermodynamic modelling. •Destabilisation of ettringite above 50 °C correlates with sulphate content of C–S–H

  20. Effect of temperature on the hydration of Portland cement blended with siliceous fly ash

    Energy Technology Data Exchange (ETDEWEB)

    Deschner, Florian, E-mail: florian.deschner@gmail.com [Empa, Swiss Federal Laboratories for Materials Science and Technology, Laboratory for Concrete and Construction Chemistry, Überlandstrasse 129, 8600 Dübendorf (Switzerland); Lothenbach, Barbara; Winnefeld, Frank [Empa, Swiss Federal Laboratories for Materials Science and Technology, Laboratory for Concrete and Construction Chemistry, Überlandstrasse 129, 8600 Dübendorf (Switzerland); Neubauer, Jürgen [GeoZentrum Nordbayern, Mineralogy, University of Erlangen-Nuremberg, 91054 Erlangen (Germany)

    2013-10-15

    The effect of temperature on the hydration of Portland cement pastes blended with 50 wt.% of siliceous fly ash is investigated within a temperature range of 7 to 80 °C. The elevation of temperature accelerates both the hydration of OPC and fly ash. Due to the enhanced pozzolanic reaction of the fly ash, the change of the composition of the C–S–H and the pore solution towards lower Ca and higher Al and Si concentrations is shifted towards earlier hydration times. Above 50 °C, the reaction of fly ash also contributes to the formation of siliceous hydrogarnet. At 80 °C, ettringite and AFm are destabilised and the released sulphate is partially incorporated into the C–S–H. The observed changes of the phase assemblage in dependence of the temperature are confirmed by thermodynamic modelling. The increasingly heterogeneous microstructure at elevated temperatures shows an increased density of the C–S–H and a higher coarse porosity. -- Highlights: •The reaction of quartz powder at 80 °C strongly enhances the compressive strength. •Almost no strength increase of fly ash blended OPC at 80 °C was found after 2 days. •Siliceous hydrogarnet is formed upon the reaction of fly ash at high temperatures. •Temperature dependent change of the system was simulated by thermodynamic modelling. •Destabilisation of ettringite above 50 °C correlates with sulphate content of C–S–H.

  1. 3D Computational Simulation of Calcium Leaching in Cement Matrices

    Directory of Open Access Journals (Sweden)

    Gaitero, J. J.

    2014-12-01

    Full Text Available Calcium leaching is a degradation process consisting in progressive dissolution of the cement paste by migration of calcium atoms to the aggressive solution. It is therefore, a complex phenomenon involving several phases and dissolution and diffusion processes simultaneously. Along this work, a new computational scheme for the simulation of the degradation process in three dimensions was developed and tested. The toolkit was used to simulate accelerated calcium leaching by a 6M ammonium nitrate solution in cement matrices. The obtained outputs were the three dimensional representation of the matrix and the physicochemical properties of individual phases as a consequence of the degradation process. This not only makes it possible to study the evolution of such properties as a function of time but also as a function of the position within the matrix. The obtained results are in good agreement with experimental values of the elastic modulus in degraded and undegraded samples.El lixiviado de calcio es un proceso de degradación consistente en la disolución progresiva de la pasta de cemento por la migración de los átomos de calcio a la disolución agresiva. Se trata por tanto de un fenómeno complejo que involucra simultáneamente diferentes fases y procesos de disolución y difusión. En este trabajo se desarrolló y probó una nueva herramienta computacional para la simulación del proceso de degradación en tres dimensiones. Para ello se simuló el lixiviado de calcio acelerado provocado por una disolución de nitrato amónico 6M en matrices de cemento. Como resultado se obtuvieron la representación tridimensional de la matriz y las propiedades físico-químicas sus fases a lo largo del tiempo. Esto permitió estudiar la evolución de dichas propiedades a lo largo del proceso de degradación así como en función de su posición dentro de la matriz. Los resultados obtenidos coinciden con los valores experimentales del módulo elástico tanto

  2. Investigating calcium polyphosphate addition to a conventional calcium phosphate cement for bone-interfacing applications

    Science.gov (United States)

    Krausher, Jennifer Lynn

    Calcium phosphate cements (CPCs) are of great interest in bone regeneration applications because of their biocompatibility and osteoconductivity, and as delivery vehicles for therapeutics; however, delivery applications have been limited by adverse interactions between therapeutics and the cement setting reaction. Amorphous calcium polyphosphate (CPP) yields a biodegradable material with a demonstrated drug delivery capacity following appropriate processing. The incorporation of drug-loaded CPP into a CPC is under consideration as a method of minimizing adverse interactions and extending drug release. This thesis represents the first investigation into the effects of CPP addition on the properties, setting and antibiotic release profile of a conventional apatitic calcium phosphate cement. As-made, gelled and vancomycin-loaded CPP particulate were added to the powder component of a conventional dicalcium phosphate/tetracalcium phosphate CPC. The setting behaviour, set properties and microstructure of the resulting CPP-CPCs were evaluated with setting time testing (Gilmore needle method), pH testing, mechanical testing, SEM imaging, XRD and FTIR analysis. In vitro degradation and elution behaviour were evaluated by monitoring calcium release (atomic absorbance spectroscopy), mechanical strength and vancomycin release (UV-visual spectrophotometry). CPP addition was found to increase the setting time, reduce the mechanical strength and inhibit the conversion of the CPC starting powders to the set apatitic phase. The most likely mechanism for the observed effect of CPP addition was the adsorption of polyphosphate chains on the particle surfaces, which would inhibit the dissolution of the starting powders and the conversion of apatite precursor phases to apatite, leading to reduced mechanical properties. The detrimental effects of CPP were reduced by limiting the CPP fraction to less than a few weight per cent and increasing the size of the CPP particulate. CPP

  3. Growth of a bonelike apatite on chitosan microparticles after a calcium silicate treatment

    OpenAIRE

    Leonor, I. B.; Baran, E. T.; Kawashita, M.; Reis, R. L.; T Kokubo; Nakamura, T

    2008-01-01

    Bioactive chitosan microparticles can be prepared successfully by treating them with a calcium silicate solution and then subsequently soaking them in simulated body fluid (SBF). Such a combination enables the development of bioactive microparticles that can be used for several applications in the medical field, including injectable biomaterial systems and tissue engineering carrier systems. Chitosan microparticles, 0.6 lm in average size, were soaked either for 12 h in fresh calcium...

  4. The use of calcium phosphate cement in vertebroplasty of the base of odontoid process.

    Science.gov (United States)

    Zapałowicz, Krzysztof; Wojdyn, Maciej; Zieliński, Krzysztof Włodzimierz; Snopkowska-Wiaderna, Dorota

    2013-01-01

    The authors describe the use of bone cement containing calcium phosphate for vertebroplasty of the cavity in the base of odontoid process. A 23-year-old female patient was operated on by incision in lateral cervical area (anterior open access). After a blunt dissection, the working cannula (Kyphon) was introduced under fluoroscopic guidance through the C2 vertebral body to the cavity in the base of the odontoid process. Intraoperatively, biopsy of the lesion was taken and histo-pathological examination excluded the presence of neoplasm. The cavity, presumably haemangioma, was successfully filled with calcium phosphate bone cement KyphOsTM FS (Ky-phon). The proper filling without paravertebral cement leak was confirmed by postoperative computed tomography (CT). The CT and magnetic resonance imaging performed 9 months after the procedure showed that cement was still present in the cavity. This is the first use of calcium phosphate cement to conduct the vertebroplasty of C2 vertebra. PMID:24375006

  5. Clinical and Radiographic Assessment of the Efficacy of Calcium Silicate Indirect Pulp Capping

    Science.gov (United States)

    Hashem, D.; Mannocci, F.; Patel, S.; Manoharan, A.; Brown, J.E.; Watson, T.F.

    2015-01-01

    The aims of this study were to assess the effectiveness of calcium silicate cement (Biodentine) versus glass ionomer cement (GIC; control group) as indirect pulp capping materials in patients with reversible pulpitis and to compare the effectiveness of cone beam computed tomography (CBCT) versus periapical (PA) radiographs in detecting PA changes at baseline (T0) and at 12 mo (T12) postoperatively. Seventy-two restorations (36 Biodentine, 36 Fuji IX) were placed randomly in 53 patients. CBCT/PA radiographs were taken at T0 and T12. Two calibrated examiners assessed the presence/absence and increase/decrease in the size of existing PA radiolucencies under standardized conditions. The Kappa coefficient evaluated statistically the effectiveness of CBCT versus PA radiographs in detecting PA changes. Chi-square/Mann-Whitney tests were used to evaluate the association between PA changes in CBCT with various clinical measures. Significance was predetermined at α = 0.05. Clinical success rates for Biodentine and Fuji IX GIC were 83.3%. CBCT was significantly more effective in detecting PA radiolucencies compared with radiographs (P = 0.0069). Of the teeth, 65.4% and 90.4% were deemed healthy using CBCT and PA radiographs, respectively, at T12. Healing/healed rates were 17.3%/0%, while new/progressed radiolucency were 30.8%/9.6% with CBCT/PA radiographs, respectively. Seventy-one percent of healed lesions had received Biodentine; 88% of new/progressed lesions received Fuji IX GIC. Teeth presenting with an initial CBCT PA lesion had a failure rate of 63%, whereas teeth with no initial lesion had a failure rate of 16%. Although no statistically significant difference was detected in the clinical efficacy of Biodentine/Fuji IX when used as indirect pulp capping materials in patients with reversible pulpitis, CBCT showed a significant difference in that most healed CBCT lesions had received Biodentine while most that did not heal received Fuji IX. Longer-term follow-up is

  6. Polyelectrolyte addition effect on the properties of setting hydraulic cements based on calcium phosphate

    International Nuclear Information System (INIS)

    In the present work the effects of the addition of some poly electrolytes (sodium alginate and poly acrylic acid) on the solubility, crystalline phases, pH and mechanical strength under compression of three calcium phosphate cements were studied. (author)

  7. Balloon vetebroplasty with calcium phosphate cement augmentation for direct restoration of traumatic thoracolumbar vertebral fractures

    NARCIS (Netherlands)

    Verlaan, JJ; van Helden, WH; Oner, FC; Verbout, AJ; Dhert, WJA

    2002-01-01

    Study Design. A human cadaveric model was used to evaluate balloon vertebroplasty in traumatic vertebral fractures. Objectives. To assess the feasibility and safety of balloon vertebroplasty followed by calcium phosphate cement augmentation to prevent recurrent kyphosis. Summary of Background Data.

  8. Thermal conductivity measurements on xonotlite-type calcium silicate by the transient hot-strip method

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    The experimental results of the thermal conductivities of xonotlite-type calcium silicate insulation materials were presented at different temperatures and pressures.Two appropriative surroundings,i.e.an elevated temperature surrounding from ambient temperature to 1450 K and a vacuum surrounding from atmosphere pressure to 10-3 Pa,were designed for the transient hot-strip (THS) method.The thermal conduetivities of xonotlite-type calcium silicate with four densities from ambient temperature to 1000 K and 0.045 Pa to atmospheric pressure were measured.The results show that the thermal conductivity of xunotlite-type calcium silicate decreases apparently with the fall of density,and decreases apparently with the drop of pressure,and reaches the least value at about 100 Pa.The thermal conductivity of xonotlite-type calcium silicate increases almost linearly with T3,and increases more abundantly with low density than with high density.The thermal conductivity measurement uncertainty is estimated to be approximately 3% at ambient temperature,and 6% at 800 K.

  9. Cementation of Radioactive Waste from a PWR with Calcium Sulfoaluminate Cement

    International Nuclear Information System (INIS)

    Spent radioactive ion-exchange resin (SIER) and evaporation concentrates are radioactive wastes that are produced at by pressurized water reactor (PWR) nuclear power stations. Borate, which is used as a retardent for cement, is also present as a moderator in a PWR, therefore, borate will be present in both ion-exchange resins and evaporation concentrates. In this study the use of Calcium sulfoaluminate cements (SAC) as encapsulation medium for these waste streams was investigated. The study involved the manufacturing of different cement test samples with different amounts of SAC cement, waste resins (50% water content) and admixtures. In order to reduce hydration heat during 200 L solidification experiments, different admixtures were investigated. Initial results based on compressive strength tests and hydration temperature studies, indicated that zeolite was the best admixture for the current waste form. Experiments indicated that the addition of resin material into the current cement matrix reduces the hydration heat during curing Experimental results indicated that a combination of SAC (35 wt. %), zeolite (7 wt. %) mix with 42 wt. % resins (50% water content) and 16 wt. % of water forms a optimum cured monolith with low hydration heat. The microstructures of hydrated OPC, SAC and SAC with zeolite addition were studied using a Scanning Electron Microscopy (SEM). SEM results indicated that the SAC matrices consist of a needle type structure that changed gradually into a flake type structure with the addition of zeolite. Additionally, the presence of zeolite material inside the SAC matrix reduced the leaching rates of radionuclides significantly. In a final 200 L grouting test, measured results indicated a hydration temperature below 90oC withno thermal cracks after solidified. The influence of radiation on the compressive strength and possible gas generation (due to radiolysis) on cement waste forms containing different concentrations ion exchange resin was

  10. Caesium immobilization in hydrated calcium-silicate-aluminate systems

    International Nuclear Information System (INIS)

    A special field of application of cementitious materials in using cements for immobilization of low and medium level radioactive wastes. Clarification of mechanisms of binding is complicated by the multicomponent nature of the solidifying matrix. In the present work, interest is turned to one of the most difficult to confine, long half-life isotopes, the caesium isotope. The cement matrix for solidification of the radioactive waste can be considered, with simplification, as a CaO-SiO2-Al2O3-H2O system. The various compositions of hydrated cementitious assemblages were investigated with respect to their Cs sorption by measuring the Cs distribution ratios (Rd) therein. Trends in sorption properties were detected, and the section of the ternary phase diagram with the best performance was identified

  11. Accelerated growth of calcium silicate hydrates: Experiments and simulations

    International Nuclear Information System (INIS)

    Despite the usefulness of isothermal calorimetry in cement analytics, without any further computations this brings only little information on the nucleation and growth of hydrates. A model originally developed by Garrault et al. is used in this study in order to simulate hydration curves of cement obtained by calorimetry with different known hardening accelerators. The limited basis set of parameters used in this model, having a physical or chemical significance, is valuable for a better understanding of mechanisms underlying in the acceleration of C-S-H precipitation. Alite hydration in presence of four different types of hardening accelerators was investigated. It is evidenced that each accelerator type plays a specific role on one or several growth parameters and that the model may support the development of new accelerators. Those simulations supported by experimental observations enable us to follow the formation of the C-S-H layer around grains and to extract interesting information on its apparent permeability.

  12. Performance characteristics of concrete based on a ternary calcium sulfoaluminate–anhydrite–fly ash cement

    OpenAIRE

    Ioannou, Socrates; Paine, Kevin; Reig Cerdá, Lucía; Quillin, Keith

    2015-01-01

    This paper reports an assessment of the performance of concrete based on a calcium sulfoaluminate–anhydrite–fly ash cement combination. Concretes were prepared at three different w/c ratios and the properties were compared to those of Portland cement and blast-furnace cement concretes. The assessment involved determination of mechanical and durability properties. The results suggest that an advantageous synergistic effect between and ettringite and fly ash (Ioannou et al., 2014) was reflected...

  13. Molecular mechanism of crystallization impacting calcium phosphate cements

    Energy Technology Data Exchange (ETDEWEB)

    Giocondi, J L; El-Dasher, B S; Nancollas, G H; Orme, C A

    2009-05-31

    In summary, SPM data has shown that (1) Mg inhibits growth on all steps but relatively high Mg/Ca ratios are needed. Extracting the mechanism of interaction requires more modeling of the kinetic data, but step morphology is consistent with incorporation. (2) Citrate has several effects depending on the citrate/Ca ratio. At the lowest concentrations, citrate increases the step free energy without altering the step kinetics; at higher concentrations, the polar step is slowed. (3) Oxalate also slows the polar step but additionally stabilizes a new facet, with a [100]{sub Cc} step. (4) Etidronate has the greatest kinetic impact of the molecules studied. At 7{micro}M concentrations, the polar step slows by 60% and a new polar step appears. However, at the same time the [10-1]{sub Cc} increases by 67%. It should be noted that all of these molecules complex calcium and can effect kinetics by altering the solution supersaturation or the Ca to HPO{sub 4}{sup 2-} ratio. For the SPM data shown, this effect was corrected for to distinguish the effect of the molecule at the crystal surface from the effect of the molecule on the solution speciation. The goal of this paper is to draw connections between fundamental studies of atomic step motion and potential strategies for materials processing. It is not our intent to promote the utility of SPM for investigating processes in cement dynamics. The conditions are spectacularly different in many ways. The data shown in this paper are fairly close to equilibrium (S=1.6) whereas the nucleation of cements is initiated at supersaturation ratios in the thousands to millions. Of course, after the initial nucleation phase, the growth will occur at more modest supersaturations and as the cement evolves towards equilibrium certainly some of the growth will occur in regimes such as shown here. In addition to the difference in supersaturation, cements tend to have lower additive to calcium ratios. As an example, the additive to Ca ratio is

  14. Multiple characterization study on porosity and pore structure of calcium phosphate cements

    OpenAIRE

    Pastorino Carraz, David; Canal Barnils, Cristina; Ginebra Molins, Maria Pau

    2015-01-01

    Characterization of the intricate pore structure of calcium phosphate cements is a key step to successfully link the structural properties of these synthetic bone grafts with their most relevant properties, such as in vitro or in vivo behaviour, drug loading and release properties, or degradation over time. This is a challenging task due to the wide range of pore sizes in calcium phosphate cements, compared to most other ceramic biomaterials. This work provides a critical assessment of three ...

  15. An injectable calcium phosphate cement for the local delivery of paclitaxel to bone

    NARCIS (Netherlands)

    Lopez-Heredia, M.A.; Kamphuis, G.J.; Thune, P.C.; Oner, F.C.; Jansen, J.A.; Walboomers, X.F.

    2011-01-01

    Bone metastases are usually treated by surgical removal, fixation and chemotherapeutic treatment. Bone cement is used to fill the resection voids. The aim of this study was to develop a local drug delivery system using a calcium phosphate cement (CPC) as carrier for chemotherapeutic agents. CPC cons

  16. On the nature of structural disorder in calcium silicate hydrates with a calcium/silicon ratio similar to tobermorite

    OpenAIRE

    Grangeon, Sylvain; Claret, Francis; Lerouge, Catherine; Warmont, Fabienne; SATO, Tsutomo; ANRAKU, Sohtoru; Numako, Chiya; LINARD, Yannick; Lanson, Bruno

    2013-01-01

    Four calcium silicate hydrates (C-S-H) with structural calcium/silicon (Ca/Si) ratios ranging from 0.82 +/- 0.02 to 0.87 +/- 0.02 were synthesized at room temperature, 50, 80, and 110 degrees C. Their structure was elucidated by collating information from electron probe micro-analysis, transmission electron microscopy, extended X-ray absorption fine structure spectroscopy, and powder X-ray diffraction (XRD). A modeling approach specific to defective minerals was used because sample turbostrat...

  17. BLENDED CALCIUM ALUMINATE-CALCIUM SULFATE CEMENT-BASED GROUT FOR P-REACTOR VESSEL IN-SITU DECOMMISSIONING

    Energy Technology Data Exchange (ETDEWEB)

    Langton, C.; Stefanko, D.

    2011-03-10

    The objective of this report is to document laboratory testing of blended calcium aluminate - calcium hemihydrate grouts for P-Reactor vessel in-situ decommissioning. Blended calcium aluminate - calcium hemihydrate cement-based grout was identified as candidate material for filling (physically stabilizing) the 105-P Reactor vessel (RV) because it is less alkaline than portland cement-based grout which has a pH greater than 12.4. In addition, blended calcium aluminate - calcium hemihydrate cement compositions can be formulated such that the primary cementitious phase is a stable crystalline material. A less alkaline material (pH {<=} 10.5) was desired to address a potential materials compatibility issue caused by corrosion of aluminum metal in highly alkaline environments such as that encountered in portland cement grouts [Wiersma, 2009a and b, Wiersma, 2010, and Serrato and Langton, 2010]. Information concerning access points into the P-Reactor vessel and amount of aluminum metal in the vessel is provided elsewhere [Griffin, 2010, Stefanko, 2009 and Wiersma, 2009 and 2010, Bobbitt, 2010, respectively]. Radiolysis calculations are also provided in a separate document [Reyes-Jimenez, 2010].

  18. Blended Calcium Aluminate-Calcium Sulfate Cement-Based Grout For P-Reactor Vessel In-Situ Decommissioning

    International Nuclear Information System (INIS)

    The objective of this report is to document laboratory testing of blended calcium aluminate - calcium hemihydrate grouts for P-Reactor vessel in-situ decommissioning. Blended calcium aluminate - calcium hemihydrate cement-based grout was identified as candidate material for filling (physically stabilizing) the 105-P Reactor vessel (RV) because it is less alkaline than portland cement-based grout which has a pH greater than 12.4. In addition, blended calcium aluminate - calcium hemihydrate cement compositions can be formulated such that the primary cementitious phase is a stable crystalline material. A less alkaline material (pH ≤ 10.5) was desired to address a potential materials compatibility issue caused by corrosion of aluminum metal in highly alkaline environments such as that encountered in portland cement grouts (Wiersma, 2009a and b, Wiersma, 2010, and Serrato and Langton, 2010). Information concerning access points into the P-Reactor vessel and amount of aluminum metal in the vessel is provided elsewhere (Griffin, 2010, Stefanko, 2009 and Wiersma, 2009 and 2010, Bobbitt, 2010, respectively). Radiolysis calculations are also provided in a separate document (Reyes-Jimenez, 2010).

  19. Developments in TEM Nanotomography of Calcium Silicate Hydrate

    KAUST Repository

    Taylor, Rae

    2015-04-01

    This investigation was designed to explore the possibility of using transmission electron microscope (TEM) tomography on cement-based systems gain a greater understanding of their nanostructure and pore network. The preliminary results show a clearly a well-defined pore network at the nanoscale, with pore size approximately 1.7-2.4 nm in diameter and spaced around 5-8 nm apart. A comparison of small angle X-ray scattering data with 2-D TEM images analyzed with the Fourier slice theorem documents an excellent structural correlation. © 2015 The American Ceramic Society.

  20. Activity diagrams for calcium/hydrogen, sodium/hydrogen, and potassium/hydrogen, and H4SiO4 and their relation to reactions in systems containing radioactive waste forms, cement, and rock in the presence of water

    International Nuclear Information System (INIS)

    In order to identify reactions which can occur in systems containing nuclear waste forms, cement, and repository rock in the presence of water, activity diagrams were calculated from free energies for aluminosilicates and calcium silicates. Groundwater compositions from candidate repository sites in the Palo Duro Basin of Texas, the Delaware Basin of New Mexico, and the Nevada Test Site were plotted on these diagrams. Essentially all of these are shown to be in the calcium zeolite field as shown on the diagram for calcium in the absence of other cations. Chlorite is shown to be stable in this region at the Mg and pH level of the Ogallala if the chlorite is high in iron, and at the Mg and pH level of the Wolfcamp low- or high-Fe chlorites are stable. Potassium and sodium mineral relationships fall in two categories, dilute waters and saline waters. Boreholes at Yucca Flat and Mercury Valley at the Nevada Test Site, and shallow ground water from the Rolling Plains north and east of the Palo Duro Basin are in equilibrium with kaolinite. The brines from the Salado and Rustler formations are in equilibrium with kaolinite and possibly also with sodium-potassium zeolite and illite. Leachates of cement and water, and cement, waste, and water were plotted on the calcium silicate activity diagram. These solutions are in equilibrium with calcium silicate hydrate hydrolysis reactions, with grossular and possibly with Ca-zeolites. Among the calcium silicates, calcium-silicate-hydrate gel (C-S-H gel) and tobermorite are the most likely candidates, but the thermodynamic data are not adequate to distinguish all the possibilities. 37 references, 4 figures, 3 tables

  1. Santaclaraite, a new calcium-manganese silicate hydrate from California.

    Science.gov (United States)

    Erd, Richard C.; Ohashi, Y.

    1984-01-01

    Santaclaraite, ideally CaMn4(Si5O14(OH))(OH).H2O, occurs as pink and tan veins and masses in Franciscan chert in the Diablo Range, Santa Clara and Stanislaus counties, California. It is associated with four unidentified Mn silicates, Mn-howieite, quartz, braunite, calcite, rhodochrosite, kutnahorite, baryte, harmotome, chalcopyrite and native copper. Santaclaraite is triclinic, space group B1, a 15.633(1), b 7.603(1) , c 12.003(1) A, alpha 109.71(1)o, beta 88.61(1)o, gamma 99.95(1) o, V 1322.0(3) A3; Z = 4. The strongest lines of the X-ray pattern are 7.04(100), 3.003(84), 3.152(80), 7.69(63), 3.847(57) A. Crystals are lamellar to prismatic (flattened on (100)), with good cleavage on (100) and (010); H. 61/2 Dcalc. 3.398 g/cm3, Dmeas. 3.31 (+ or -0.01); optically biaxial negative, alpha 1.681, beta 1.696, gamma 1.708 (all + or - 0.002), 2Valpha 83 (+ or -1)o. Although chemically a hydrated rhodonite, santaclaraite dehydrates to Mn-bustamite at approx 550oC (in air) . Santaclaraite is a five-tetrahedral-repeat single-chain silicate and has structural affinities with rhodonite, nambulite, marsturite, babingtonite and inesite.-J.A.Z.

  2. The effects of citric acid on the hydration of calcium phosphate cement

    Institute of Scientific and Technical Information of China (English)

    DAI Hong-lian; YAN Yu-hua; WANG You-fa; LI Shi-pu

    2001-01-01

    @@ INTRODUCTION Calcium phosphate cements (CPC) overcome the practical disadvantages of blocks or granulesl can be handled as a paste and sit in situ. Their structure and composition close to that of HAP make them biocompatible materials. 2 The conventional calcium phosphate cement had some problems such as long setting time (30~60 min) and low compressive strength, etc. In our system, an α-TCP/TTCP powder mixture was mixed with water containing citric acid to control the setting time and compressive strength. In this paper, the effects of various concentration citric acid solutions on the properties of the cement are reported.

  3. Effect of different retarders on the hydration of calcium sulfoaluminate eco-cement pastes

    OpenAIRE

    García-Maté, Marta; De la Torre, Ángeles G.; Aranda, Miguel A. G.; Santacruz, Isabel

    2014-01-01

    The manufacture of Calcium SulfoAluminate (CSA) cements is more environmentally friendly than that of OPC [1] as their production releases up to 40% less CO2 than the latter. The main performances of CSA cements are fast setting time, good-chemical resistance properties and high early strengths. CSA cements are prepared by mixing CSA clinker with different amounts of a calcium sulfate set regulator such as gypsum (CaSO4•2H2O), bassanite (CaSO4•½H2O), or anhydrite (CaSO4), or mixtures of th...

  4. Formation of magnesium silicate hydrate (M-S-H) cement pastes using sodium hexametaphosphate

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Tingting [Faculty of Infrastructure Engineering, Dalian University of Technology, Dalian 116024 (China); Department of Materials, Centre for Advanced Structural Ceramics, Imperial College London, South Kensington Campus, London SW7 2AZ (United Kingdom); Department of Civil and Environmental Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ (United Kingdom); Vandeperre, Luc J. [Department of Materials, Centre for Advanced Structural Ceramics, Imperial College London, South Kensington Campus, London SW7 2AZ (United Kingdom); Cheeseman, Christopher R., E-mail: c.cheeseman@imperial.ac.uk [Department of Civil and Environmental Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ (United Kingdom)

    2014-11-15

    Magnesium silicate hydrate (M-S-H) gel is formed by the reaction of brucite with amorphous silica during sulphate attack in concrete and M-S-H is therefore regarded as having limited cementing properties. The aim of this work was to form M-S-H pastes, characterise the hydration reactions and assess the resulting properties. It is shown that M-S-H pastes can be prepared by reacting magnesium oxide (MgO) and silica fume (SF) at low water to solid ratio using sodium hexametaphosphate (NaHMP) as a dispersant. Characterisation of the hydration reactions by x-ray diffraction and thermogravimetric analysis shows that brucite and M-S-H gel are formed and that for samples containing 60 wt.% SF and 40 wt.% MgO all of the brucites react with SF to form M-S-H gel. These M-S-H cement pastes were found to have compressive strengths in excess of 70 MPa.

  5. Formation of magnesium silicate hydrate (M-S-H) cement pastes using sodium hexametaphosphate

    International Nuclear Information System (INIS)

    Magnesium silicate hydrate (M-S-H) gel is formed by the reaction of brucite with amorphous silica during sulphate attack in concrete and M-S-H is therefore regarded as having limited cementing properties. The aim of this work was to form M-S-H pastes, characterise the hydration reactions and assess the resulting properties. It is shown that M-S-H pastes can be prepared by reacting magnesium oxide (MgO) and silica fume (SF) at low water to solid ratio using sodium hexametaphosphate (NaHMP) as a dispersant. Characterisation of the hydration reactions by x-ray diffraction and thermogravimetric analysis shows that brucite and M-S-H gel are formed and that for samples containing 60 wt.% SF and 40 wt.% MgO all of the brucites react with SF to form M-S-H gel. These M-S-H cement pastes were found to have compressive strengths in excess of 70 MPa

  6. Development of Magnesium Silicate Hydrate cement system for nuclear waste encapsulation

    International Nuclear Information System (INIS)

    A novel low pH cement system for encapsulating nuclear industry wastes containing aluminium has been developed using blends of MgO and silica fume (SF). Identification of the hydrated phases in MgO/silica fume samples showed that brucite formed in early stages of hydration and then reacted with the silica fume to produce a magnesium silicate hydrate (M-S-H) gel phase. When all brucite reacts with silica fume a cement system with an equilibrium pH just below 10 was achieved. Selected mixes have been characterized for hydration reactions, setting time and strength development. Mortar samples with w/s ratios of 0.5 and 50% by weight of sand added achieved compressive strengths in excess of 95 MPa after 28 days. The addition of MgCO3 buffered the early pH and the addition of fine sand particles eliminated shrinkage cracking. The interaction of the optimised mortar with Al metal has been investigated. Al metal strips were firmly bound into the MgO:SF:sand samples and no H2 gas detected, and this indicates that the novel systems developed in this work have potential for encapsulating certain types of problematic legacy wastes from the nuclear industry. (authors)

  7. Structure alteration of C-S-H (calcium silicate hydrated phases) caused by sorption of caesium

    International Nuclear Information System (INIS)

    The sorption behavior of Cs onto C-S-H (calcium silicate hydrated phases) was investigated by evaluating the effect of sorption on the C-S-H structure. The C-S-H have a tobermorite-type layer structure. Each layer consists of central calcium and oxygen atoms sandwiched by silicate tetrahedral chains. Additional calcium and water are located in interlayer zones. The XRD spectra showed that the tobermorite-type layer degraded and that the sorption of Cs made the fragments of layer intergrowths much smaller. The fragmentation of the tobermorite-type layer was observed for C-S-H in contact with CsCl solution or with CsOH solution, but not for the C-S-H in contact with Na solution. Furthermore, 29Si NMR spectroscopy revealed that the sorption of Cs onto C-S-H induced cleavages of silicate chains in C-S-H. It was also suggested that the OH- ion contributed to breaking the silicate chains. (orig.)

  8. Fabrications of zinc-releasing biocement combining zinc calcium phosphate to calcium phosphate cement.

    Science.gov (United States)

    Horiuchi, Shinya; Hiasa, Masahiro; Yasue, Akihiro; Sekine, Kazumitsu; Hamada, Kenichi; Asaoka, Kenzo; Tanaka, Eiji

    2014-01-01

    Recently, zinc-releasing bioceramics have been the focus of much attention owing to their bone-forming ability. Thus, some types of zinc-containing calcium phosphate (e.g., zinc-doped tricalcium phosphate and zinc-substituted hydroxyapatite) are examined and their osteoblastic cell responses determined. In this investigation, we studied the effects of zinc calcium phosphate (ZCP) derived from zinc phosphate incorporated into calcium phosphate cement (CPC) in terms of its setting reaction and MC3T3-E1 osteoblast-like cell responses. Compositional analysis by powder X-ray diffraction analysis revealed that HAP crystals were precipitated in the CPC containing 10 or 30wt% ZCP after successfully hardening. However, the crystal growth observed by scanning electron microscopy was delayed in the presence of additional ZCP. These findings indicate that the additional zinc inhibits crystal growth and the conversion of CPC to the HAP crystals. The proliferation of the cells and alkaline phosphatase (ALP) activity were enhanced when 10wt% ZCP was added to CPC. Taken together, ZCP added CPC at an appropriate fraction has a potent promotional effect on bone substitute biomaterials. PMID:24090874

  9. Attributes of the soil fertilized with sewage sludge and calcium and magnesium silicate

    OpenAIRE

    Geraldo R. Zuba Junio; Regynaldo A. Sampaio; Altina L. Nascimento; Luiz A. Fernandes; Natália N. de Lima; João P. Carneiro

    2015-01-01

    ABSTRACTThis study aimed to evaluate the chemical attributes of an Inceptisol cultivated with castor bean (Ricinus communis L.), variety ‘BRS Energia’, fertilized with sewage sludge compost and calcium (Ca) and magnesium (Mg) silicate. The experiment was conducted at the ICA/UFMG, in a randomized block design, using a 2 x 4 factorial scheme with three replicates, and the treatments consisted of two doses of Ca-Mg silicate (0 and 1 t ha-1) and four doses of sewage sludge compost (0, 23.81, 47....

  10. Mechanical Properties and Durability of Advanced Environmental Barrier Coatings in Calcium-Magnesium-Alumino-Silicate Environments

    Science.gov (United States)

    Miladinovich, Daniel S.; Zhu, Dongming

    2011-01-01

    Environmental barrier coatings are being developed and tested for use with SiC/SiC ceramic matrix composite (CMC) gas turbine engine components. Several oxide and silicate based compositons are being studied for use as top-coat and intermediate layers in a three or more layer environmental barrier coating system. Specifically, the room temperature Vickers-indentation-fracture-toughness testing and high-temperature stability reaction studies with Calcium Magnesium Alumino-Silicate (CMAS or "sand") are being conducted using advanced testing techniques such as high pressure burner rig tests as well as high heat flux laser tests.

  11. Synthesis of pure zeolite P2 from calcium silicate hydrate; tobermorite

    Directory of Open Access Journals (Sweden)

    Nasser Y. Mostafa

    2015-06-01

    Full Text Available Calcium silicate hydrate phases offer the possibility to become potential zeolites precursors due to its high silica contents. Pure calcium silicate hydrate phase; tobermorite (Ca5Si6O16(OH2·4H2O, was prepared by hydrothermal method at 175°C. Tobermorite was sucssefully converted to Zeolite P2 for the first time via refluxing in 3 M NaOH solution and in the presence of Al source. Sodium hydroxide removed calcium ions from the interlayers of calcium silicate phase and form mesoporous zeolite. The pure zeolite was obtained after extraction of Ca(OH2 with sugar solution. The zeolite products were characterized by using X-ray diffraction spectroscopy (XRD and Scanning Electron Microscopy (SEM with microanalysis (EDX. The Si/Al molar ratio of zeolite P can be controlled by vering the initinal Si/Al molar ratio. The cation-exchange capacity (CEC of the produced zeolite P was higher than those produced from fly ash.

  12. Low-temperature fabrication of macroporous scaffolds through foaming and hydration of tricalcium silicate paste and their bioactivity

    OpenAIRE

    Huan, Z.; Chang, J.; Zhou, J.

    2009-01-01

    A low-temperature fabrication method for highly porous bioactive scaffolds was developed. The two-step method involved the foaming of tricalcium silicate cement paste and hydration to form calcium silicate hydrate and calcium hydroxide. Scaffolds with a combination of interconnected macro- and micro-sized pores were fabricated by making use of the decomposition of a hydrogen peroxide (H2O2) solution that acted as a foaming agent and through the hydration of tricalcium silicate cement. It was ...

  13. Evaluation of Calcium Phosphate Cement As a Root Canal Sealer Filling Material

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Calcium phosphate cement for root end sealing was obtained by mixing α-tricalcium phosphate and additives with an aqueous solution of citric. Powder and liquid were mixed at a ratio of 1.25g/mL. The biocompatibility of this material was investigated primarily by subcutaneous implantation tests. Then calcium phosphate cement was used to fill three adult dogs' root canal, both calcium hydroxide paste and hydroxyapatite paste as control. The animals were killed at 4,12,20 weeks postoperatively respectively. The effects of different materials on the apical closure, restoration of periapical tissues and adaptability to the dentinal surface were examined by optical and electronic microscope. The observation at 20 weeks shows that the calcium phosphate cement has the potentialities of being a root canal sealer filling material available for pulpless teeth with open-apex and destructive periapical tissue.

  14. A Novel Synthesis Method of Porous Calcium Silicate Hydrate Based on the Calcium Oxide/Polyethylene Glycol Composites

    Directory of Open Access Journals (Sweden)

    Wei Guan

    2013-01-01

    Full Text Available This paper proposed a novel method to prepare porous calcium silicate hydrate (CSH based on the calcium oxide/polyethylene glycol (CaO/PEG2000 composites as the calcium materials. The porosity formation mechanism was revealed via X-ray diffraction (XRD, field-emission scanning electron microscopy (FESEM, Brunauer-Emmett-Teller (BET, and Fourier transformed infrared spectroscopy (FT-IR. The reactivity of silica materials (SiO2 enhanced by increasing pH value. Ca2+ could not sustain release from CaO/PEG2000 and reacted with caused by silica to form CSH until the hydrothermal temperature reached to 170°C, avoiding the hardly dissolved intermediates formation efficiently. The as-prepared CSH, due to the large specific surface areas, exhibited excellent release capability of Ca2+ and OH−. This porous CSH has potential application in reducing the negative environmental effects of continual natural phosphate resource depletion.

  15. Synthetic crystalline calcium silicate hydrate (I): cation exchange and caesium selectivity

    International Nuclear Information System (INIS)

    Solid crystalline calcium silicate hydrate (I) synthesized from equimolar amounts of Ca and Si under hydrothermal conditions at 120 oC shows cation exchange properties towards divalent metal cations such as Ni, Cu, Cd, or Hg. It also exhibits caesium selectivity in the presence of Na+. The exchange capacity and selectivity of the solid can be increased by 10 and 28 %, respectively, upon substitution of 0.01 mol of the Ca2+ in its structure by Na+. The ability of metal cation uptake by the solid was found to obey the order Ni2+ > Hg2+ > Cu2+ > Cd2+. The different affinities of calcium silicate hydrate (I) towards these ions can be used for their separation from solutions and also in nuclear waste treatment. The mechanism of the exchange reaction is discussed. (author)

  16. In vitro biocompatibility of chitosan/hyaluronic acid-containing calcium phosphate bone cements.

    Science.gov (United States)

    Hesaraki, Saeed; Nezafati, Nader

    2014-08-01

    The need for bone repair has increased as the population ages. In this research, calcium phosphate cements, with and without chitosan (CS) and hyaluronic acid (HA), were synthesized. The composition and morphological properties of cements were evaluated by X-ray diffraction and scanning electron microscopy. The acellular in vitro bioactivity revealed that different apatite morphologies were formed on the surfaces of cements after soaking in simulated body fluid. The in vitro osteoblastic cell biocompatibility of in situ forming cements was evaluated and compared with those of conventional calcium phosphate cements (CPCs). The viability and growth rate of the cells were similar for all CPCs, but better alkaline phosphatase activity was observed for CPC with CS and HA. Calcium phosphate cements supported attachment of osteoblastic cells on their surfaces. Spindle-shaped osteoblasts with developed cytoplasmic membrane were found on the surfaces of cement samples after 7 days of culture. These results reveal the potential of the CPC-CS/HA composites to be used in bone tissue engineering. PMID:24399509

  17. Effects of Calcium Lignosulfonate and Silicic Acid on Ammonium Nitrate Degradation

    Directory of Open Access Journals (Sweden)

    Ahmet Ozan Gezerman

    2014-01-01

    Full Text Available Ammonium nitrate salts are the most commonly used nitrogenous fertilizers in industry. However, storage of ammonium nitrate is problematic, since its initial properties can decline because of environmental factors, leading to large economic losses. In this study, in order to prevent the caking and degradation of ammonium nitrate, an alternative composition with additional calcium lignosulfonate and silicic acid was studied. The resulting fertilizer was analyzed by screening analysis, ion chromatography, and electron microscopy methods.

  18. Influence of Hydrothermal Temperature on Phosphorus Recovery Efficiency of Porous Calcium Silicate Hydrate

    OpenAIRE

    Wei Guan; Fangying Ji; Qingkong Chen; Peng Yan; Weiwei Zhou

    2013-01-01

    Porous calcium silicate hydrate (PCSH) was synthesized by carbide residue and white carbon black. The influence of hydrothermal temperature on phosphorus recovery efficiency was investigated by Field Emission Scanning Electron Microscopy (FESEM), Brunauer-Emmett-Teller (BET), and X-Ray Diffraction (XRD). Hydrothermal temperature exerted significant influence on phosphorus recovery performance of PCSH. Hydrothermal temperature 170°C for PCSH was more proper to recover phosphorus. PCSH could re...

  19. Study on selective sorption of 137Cs on Al-substituted calcium silicate hydroxy hydrate

    International Nuclear Information System (INIS)

    Sorption properties have been investigated by radiometric (tracer) technique at room temperature for aluminium substituted calcium silicate hydroxy hydrate, known as tobermorite. The 137Cs selectivity has been examined in presence of 1000 times concentrated solution of Na+, Ca2+, and Ba2+. The results suggest that the title phase could be used for immobilization of radioactive cesium. Cation exchange reaction takes place mainly from edge and planar surface sites along with interlayer Ca2+ sites. (author)

  20. Biomimetic apatite deposition on polymeric microspheres treated with a calcium silicate solution

    OpenAIRE

    Leonor, I. B.; Balas, F.; Kawashita, M.; Reis, R. L.; T Kokubo; Nakamura, T

    2009-01-01

    Bioactive polymeric microspheres can be prepared by means of coating them with a calcium silicate solution and subsequently soaking in a simulated body fluid (SBF). Such combination should allow for the development of bioactive microspheres for several applications in the medical field including tissue engineering carriers. Four types of polymeric microspheres, with different sizes, were used in this work: (i) ethylene-vinyl alcohol copolymer (20–30 µm), (ii) polyamide 12 with 10% magnetite (...

  1. Biomimetic apatite formation on different polymeric microspheres modified with calcium silicate solutions

    OpenAIRE

    Leonor, I. B.; Balas, F.; Kawashita, M.; Reis, R. L.; T Kokubo; Nakamura, T

    2006-01-01

    Bioactive polymeric microspheres can be produced by pre-coating them with a calcium silicate solution and the subsequent soaking in a simulated body fluid (SBF). Such combination should allow for the development of bioactive microspheres for several applications in the medical field including tissue engineering. In this work, three types of polymeric microspheres with different sizes were used: (i) ethylene-vinyl alcohol co-polymer (20-30 'm), (ii) polyamide 12 (10-30 'm) and (...

  2. Alleviating aluminum toxicity in an acid sulfate soil from Peninsular Malaysia by calcium silicate application

    OpenAIRE

    A. A. Elisa; Ninomiya, S.; J. Shamshuddin; Roslan, I.

    2016-01-01

    In response to human population increase, the utilization of acid sulfate soils for rice cultivation is one option for increasing production. The main problems associated with such soils are their low pH values and their associated high content of exchangeable Al, which could be detrimental to crop growth. The application of soil amendments is one approach for mitigating this problem, and calcium silicate is an alternative soil amendment that could be used. Therefore, the ma...

  3. Raman thresholds and rigid to floppy transitions in calcium silicate glasses

    OpenAIRE

    Micoulaut, M.; Malki, M.; Simon, P.; Canizares, A.

    2004-01-01

    Alkaline earth silicate glasses $xCaO-(1-x)SiO_2$ exhibit a well marked threshold in Raman lineshapes which can be related to the onset of network rigidity as the concentration of calcium oxide $x$ is decreased. The present results are analyzed by constraint counting algorithms and more deeply characterized by a size increasing cluster approximation that allows to perform Maxwell mechanical constraint counting beyond the usual mean-field treatment. This permits to discuss under which structur...

  4. Alleviating aluminium toxicity on an acid sulphate soils in Peninsular Malaysia with application of calcium silicate

    OpenAIRE

    A. A. Elisa; Ninomiya, S.; J. Shamshuddin; Roslan, I.

    2015-01-01

    A study was conducted to alleviate Al toxicity of an acid sulphate soils collected from paddy cultivation area in Kedah, Peninsular Malaysia. For this purpose, the collected acid sulphate soils were treated with calcium silicate. The treated soils were incubated for 120 days in submerged condition in a glasshouse. Subsamples were collected every 30 days throughout the incubation period. Soil pH and exchangeable Al showed positive effect; soil pH increased from ...

  5. Effect of calcium triphosphate cement on proximal humeral fracture osteosynthesis: a finite element analysis.

    Science.gov (United States)

    Kennedy, Jim; Feerick, Emer; McGarry, Patrick; FitzPatrick, David; Mullett, Hannan

    2013-08-01

    PURPOSE. To measure the effect of void-filling calcium triphosphate cement on the loads at the implant-bone interface of a proximal humeral fracture osteosynthesis using a finite element analysis. METHODS. Finite element models of a 3-part proximal humeral fracture fixed with a plate with and without calcium triphosphate cement augmentation were generated from a quantitative computed tomography dataset of an intact proximal humerus. Material properties were assigned to bone fragments using published expressions relating Young's modulus to local Hounsfield number. Boundary conditions were then applied to the model to replicate the physiological loads. The effect of void-filling calcium triphosphate cement was analysed. RESULTS. When the void was filled with calcium triphosphate cement, the pressure gradient of the bone surrounding the screws in the medial fracture fragment decreased 97% from up to 21.41 to 0.66 MPa. Peak pressure of the fracture planes decreased 95% from 6.10 to 0.30 MPa and occurred along the medial aspect. The mean stress in the screw locking mechanisms decreased 78% from 71.23 to 15.92 MPa. The angled proximal metaphyseal screw had the highest stress. CONCLUSION. Augmentation with calcium triphosphate cement improves initial stability and reduces stress on the implant-bone interface. PMID:24014777

  6. Hydrothermal Synthesis of Xonotlite-type Calcium Silicate Insulation Material Using Industrial Zirconium Waste Residue

    Institute of Scientific and Technical Information of China (English)

    JIANG Jinguo; CUI Chong; LIU Jinqiang; LIAO Wenli

    2011-01-01

    Xonotlite-type insulation material was prepared by hydrothermal synthesis technology using industrial zirconium waste residue in this paper, and the phase analysis together with the observation of micro-morphology were also carried out by XRD, SEM and TEM. The density and thermal conductivity were measured finally. The results indicate, chlorine ion impurity contained in zirconium waste residue can be removed effectively via water washed process, and the reactive activity of silicon dioxide is almost not affected,which make it be a good substitution of silicon material for the preparation of calcium silicate insulation material by hydrothermal synthesis technique. The density and thermal conductivity of xonotlite-type calcium silicate insulation material obtained by hydrothermal synthesis technique can reach 159 kg/m3, 0.049 W/(m·°C), respectively, meeting with National Standard well, when synthesis conditions are selected as follows: Ca/Si molar ratio equal to 1, synthesis temperature at 210 ℃ and kept for 8 hrs. It provides a new approach to realize lightweight and low thermal conductivity of calcium silicate insulation material.

  7. On the nature of structural disorder in calcium silicate hydrates with a calcium/silicon ratio similar to tobermorite

    International Nuclear Information System (INIS)

    Four calcium silicate hydrates (C-S-H) with structural calcium/silicon (Ca/Si) ratios ranging from 0.82 ± 0.02 to 0.87 ± 0.02 were synthesized at room temperature, 50, 80, and 110 °C. Their structure was elucidated by collating information from electron probe micro-analysis, transmission electron microscopy, extended X-ray absorption fine structure spectroscopy, and powder X-ray diffraction (XRD). A modeling approach specific to defective minerals was used because sample turbostratism prevented analysis using usual XRD refinement techniques (e.g. Rietveld analysis). It is shown that C-S-H with Ca/Si ratio of ∼ 0.8 are structurally similar to nano-crystalline turbostratic tobermorite, a naturally occurring mineral. Their structure thus consists of sheets of calcium atoms in 7-fold coordination, covered by ribbons of silicon tetrahedra with a dreierketten (wollastonite-like) organization. In these silicate ribbons, 0.42 Si per bridging tetrahedron are missing. Random stacking faults occur systematically between successive layers (turbostratic stacking). Layer-to-layer distance is equal to 11.34 Å. Crystallites have a mean size of 10 nm in the a–b plane, and a mean number of 2.6–2.9 layers stacked coherently along the c* axis

  8. Conservative approach of a symptomatic carious immature permanent tooth using a tricalcium silicate cement (Biodentine): a case report

    OpenAIRE

    Villat, Cyril; Grosgogeat, Brigitte; Seux, Dominique; Farge, Pierre

    2013-01-01

    The restorative management of deep carious lesions and the preservation of pulp vitality of immature teeth present real challenges for dental practitioners. New tricalcium silicate cements are of interest in the treatment of such cases. This case describes the immediate management and the follow-up of an extensive carious lesion on an immature second right mandibular premolar. Following anesthesia and rubber dam isolation, the carious lesion was removed and a partial pulpotomy was performed. ...

  9. The determination of calcium in phosphate, carbonate, and silicate rocks by flame photometer

    Science.gov (United States)

    Kramer, Henry

    1956-01-01

    A method has been developed for the determination of calcium in phosphate, carbonate, and silicate rocks using the Beckman flame photometer, with photomultiplier attachement. The sample is dissolved in hydrofluoric, nitric, and perchloric acids, the hydrofluoric and nitric acids are expelled, a radiation buffer consisting of aluminum, magnesium, iron, sodium, potassium, phosphoric acid, and nitric acid is added, and the solution is atomized in an oxy-hydrogen flame with an instrument setting of 554 mµ. Measurements are made by comparison against calcium standards, prepared in the same manner, in the 0 to 50 ppm range. The suppression of calcium emission by aluminum and phosphate was overcome by the addition of a large excess of magnesium. This addition almost completely restores the standard curve obtained from a solution of calcium nitrate. Interference was noted when the iron concentration in the aspirated solution (including the iron from the buffer) exceeded 100 ppm iron. Other common rock-forming elements did not interfere. The results obtained by this procedure are within ± 2 percent of the calcium oxide values obtained by other methods in the range 1 to 95 percent calcium oxide. In the 0 to 1 percent calcium oxide range the method compares favorably with standard methods.

  10. Calcium aluminate cements for nuclear wastes conditioning: literature review and new approaches

    International Nuclear Information System (INIS)

    Encapsulate the diverse wastes produced by nuclear activities in cementitious binders may be very complex due to the adverse cement-waste interactions. Consequences are for example: strong delay, poor mechanical strength or low resistance to leaching. In this case, pure or blended calcium aluminate cements (CACs) may be valuable alternatives. This paper summarises the properties of CAC and blended CAC system and gives some examples from literature where calcium aluminate cements are used for conventional wastes or nuclear wastes conditioning. Moreover, it proposes another approach: using CAC not only as a binder, but also as a chemical reactant. After dissolution calcium aluminates ions can combine with many chemical species (sulphates, nitrates, chlorides, alkali metals, heavy metals) to precipitate specific hydrates allowing chemical trapping of these species. An example is given for the purification of Ni and Zn nitrates solutions. (authors)

  11. Investigation of fresh and hardened properties of Calcium sulfoaluminate (CSA) cement blends

    OpenAIRE

    Herrmann, P

    2014-01-01

    Calcium sulfoaluminate (CSA) is a comparatively new cementitious material that is mainly established in China where it is produced in a large scale. CSA cement is not covered by European standards. However, it provides different beneficial properties such as rapid hardening and high early strength development. Furthermore, the usage of CSA cement can save energy during production process in comparison to established cementitious materials. Therefore it is also more environmental friendly. ...

  12. Corrosion Resistance of Calcium Aluminate Cement Concrete Exposed to a Chloride Environment

    OpenAIRE

    Ki Yong Ann; Chang-Geun Cho

    2014-01-01

    The present study concerns a development of calcium aluminate cement (CAC) concrete to enhance the durability against an externally chemically aggressive environment, in particular, chloride-induced corrosion. To evaluate the inhibition effect and concrete properties, CAC was partially mixed with ordinary Portland cement (OPC), ranging from 5% to 15%, as a binder. As a result, it was found that an increase in the CAC in binder resulted in a dramatic decrease in the setting time of fresh concr...

  13. Device for continuous radiometric determination of the calcium and iron content in raw slurry for cement

    International Nuclear Information System (INIS)

    The characteristic iron and calcium-K series were excited using a Cd-109 isotope source. In order to determine the calcium and iron content in dry slurry, the Compton-effect scattered radiation of the Cd-109 source in the sample was used. A numerical process was worked out which allowed the elimination of the influence of changing contents of iron and water on the results of the calcium content determinations, and a device for continuous radiometric determination of calcium and iron in raw slurry was designed and constructed. The device was installed in the cement plant 'Przyjazn' under technical measuring conditions and its applicability was tested. (orig./LH)

  14. Integrated Utilization of Sewage Sludge and Coal Gangue for Cement Clinker Products: Promoting Tricalcium Silicate Formation and Trace Elements Immobilization

    Directory of Open Access Journals (Sweden)

    Zhenzhou Yang

    2016-04-01

    Full Text Available The present study firstly proposed a method of integrated utilization of sewage sludge (SS and coal gangue (CG, two waste products, for cement clinker products with the aim of heat recovery and environment protection. The results demonstrated that the incremental amounts of SS and CG addition was favorable for the formation of tricalcium silicate (C3S during the calcinations, but excess amount of SS addition could cause the impediment effect on C3S formation. Furthermore, it was also observed that the C3S polymorphs showed the transition from rhombohedral to monoclinic structure as SS addition was increased to 15 wt %. During the calcinations, most of trace elements could be immobilized especially Zn and cannot be easily leached out. Given the encouraging results in the present study, the co-process of sewage sludge and coal gangue in the cement kiln can be expected with a higher quality of cement products and minimum pollution to the environment.

  15. CALCIUM ORTHOPHOSPHATES HYDRATES: FORMATION, STABILITY AND INFLUENCE ON STANDARD PROPERTIES OF PORTLAND CEMENT

    Directory of Open Access Journals (Sweden)

    Kaziliunas A.

    2013-12-01

    Full Text Available Preparation of phosphogypsum to produce the binders requires a much higher input than preparation of natural gypsum stone. This makes it uncompetitive material. The investigations presented therein are meant to reduce this input by looking for the ways of rendering impurities harmless. Soluble acid orthophosphates are the main harmful impurity of phosphogypsum. The studies show that dry insoluble calcium orthophosphates hydrates (1.09 % and 2.18 % P2O5 in gypsum have little effect on W/C, setting times and soundness of Portland cement pastes. Insoluble calcium orthophosphates hydrates {CaHPO4∙2H2O, Ca8(HPO42(PO44∙5H2O and Ca9(HPO4(PO45(OH∙4H2O} formed in acidic medium (pH = 4.2 - 5.9 have been destroyed in alkaline medium and reduce standard compressive strength of cement up to 28 %. Calcium orthophosphates hydrates of hydroxyapatite group are stable in alcaline medium, while in dry state they reduce the standard compressive strength of cement until 10 %, but their suspensions prolong setting times of Portland cement as soluble orthophosphates – 2 - 3 times. Alkalis in cement increase pH of paste, but do not change the process of formation of calcium orthophosphates hydrates of hydroxyapatite group: it takes place through an intermediate phase - CaHPO4·2H2O, whose transformation into apatite lasts for 2 - 3 months.

  16. Effects of calcium hydroxide addition on the physical and chemical properties of a calcium silicate-based sealer

    Directory of Open Access Journals (Sweden)

    Milton Carlos KUGA

    2014-06-01

    Full Text Available Recently, various calcium silicate-based sealers have been introduced for use in root canal filling. The MTA Fillapex is one of these sealers, but some of its physicochemical properties are not in accordance with the ISO requirements. Objective: The aim of this study was to evaluate the flowability, pH level and calcium release of pure MTA Fillapex (MTAF or containing 5% (MTAF5 or 10% (MTAF10 calcium hydroxide (CH, in weight, in comparison with AH Plus sealer. Material and Methods: The flowability test was performed according to the ISO 6876:2001 requirements. For the pH level and calcium ion release analyses, the sealers were placed individually (n=10 in plastic tubes and immersed in deionized water. After 24 hours, 7 and 14 days, the water in which each specimen had been immersed was evaluated to determine the pH level changes and calcium released. Flowability, pH level and calcium release data were analyzed statistically by the ANOVA test (α=5%. Results: In relation to flowability: MTAF>AH Plus>MTAF5>MTAF10. In relation to the pH level, for 24 h: MTAF5=MTAF10=MTAF>AH Plus; for 7 and 14 days: MTAF5=MTAF10>MTAF>AH Plus. For the calcium release, for all periods: MTAF>MTAF5=MTAF10>AH Plus. Conclusions: The addition of 5% CH to the MTA Fillapex (in weight is an alternative to reduce the high flowability presented by the sealer, without interfering in its alkalization potential.

  17. Hydration of Blended Portland Cements Containing Calcium-Aluminosilicate Glass Powder and Limestone

    DEFF Research Database (Denmark)

    Moesgaard, M; Poulsen, Søren Lundsted; Herfort, D; Steenberg, M; Kirkegaard, L F; Skibsted, Jørgen; Yue, Y

    2012-01-01

    M. MOESGAARD, S.L. POULSEN, D. HERFORT, M. STEENBERG, L.F. KIRKEGAARD, J. SKIBSTED, Y. YUE, Hydration of Blended Portland Cements Containing Calcium-Aluminosilicate Glass Powder and Limestone, Journal of the American Ceramic Society 95, 403 – 409 (2012).......M. MOESGAARD, S.L. POULSEN, D. HERFORT, M. STEENBERG, L.F. KIRKEGAARD, J. SKIBSTED, Y. YUE, Hydration of Blended Portland Cements Containing Calcium-Aluminosilicate Glass Powder and Limestone, Journal of the American Ceramic Society 95, 403 – 409 (2012)....

  18. A cubic calcium oxynitrido-silicate, Ca2.89Si2N1.76O4.24

    OpenAIRE

    Ali Sharafat; Pedro Berastegui; Saeid Esmaeilzadeh; Lars Eriksson; Jekabs Grins

    2011-01-01

    The title compound, tricalcium oxynitride silicate, with composition Ca3-xSi2N2-2xO4+2x (x ≃ 0.12), is a perovskite-related calcium oxynitrido silicate containing isolated oxynitrido silicate 12-rings. The N atoms are statistically disordered with O atoms (occupancy ratio N:O = 0.88:0.12) and occupy the bridging positions in the 12 ring oxynitrido silicate anion, while the remaining O atoms are located at the terminal positions of the Si(O,N)4 tetrahedra. The majority of the Ca2+ ca...

  19. In situ synchrotron X-ray powder diffraction study of the early hydration of α-tricalcium phosphate/tricalcium silicate composite bone cement

    International Nuclear Information System (INIS)

    Bioactivity, osteogenicity and mechanical properties of α-tricalcium phosphate (α-TCP) based phosphates cements can be improved by adding tricalcium silicate (C3S); however, the addition of C3S delays the precipitation and growth of calcium deficient hydroxyapatite (CDHA). Thus, the aim of this work was the study of in situ setting reaction of α-TCP/C3S composite bone cement under high energy X-ray generated by a synchrotron source within the first 72h. The results showed that the addition of C3S induces the precipitation of nanosized CDHA at early times depending on the added content. Calculated crystallite sizes showed that the higher the content of C3S, the smaller the crystal size at the beginning of the precipitation. These results are different from those obtained by conventional XRD method, suggesting that the proposed technique is a powerful tool in determining the composition and extent of reaction of CPCs surfaces in real time. (author)

  20. In situ synchrotron X-ray powder diffraction study of the early hydration of α-tricalcium phosphate/tricalcium silicate composite bone cement

    Energy Technology Data Exchange (ETDEWEB)

    Morejon-Alonso, Loreley; Correa, Jose Raul, E-mail: lmorejon@fq.uh.cu [Departamento de Quimica General, Facultad de Quimica, Universidad de La Habana, UH (Cuba); Motisuke, Mariana [Universidade Federal de Sao Paulo (UNIFESP), Sao Jose dos Campos, SP (Brazil); Carrodeguas, Raul Garcia [Universidade Federal de Campina Grande (UFCG), Campina Grande, PB (Brazil). Laboratorio de Avaliacao e Desenvolvimento de Biomateriais do Nordeste; Santos, Luis Alberto dos [Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS (Brazil). Escola de Engenharia. Departamento de Materiais

    2015-01-15

    Bioactivity, osteogenicity and mechanical properties of α-tricalcium phosphate (α-TCP) based phosphates cements can be improved by adding tricalcium silicate (C{sub 3}S); however, the addition of C{sub 3}S delays the precipitation and growth of calcium deficient hydroxyapatite (CDHA). Thus, the aim of this work was the study of in situ setting reaction of α-TCP/C{sub 3}S composite bone cement under high energy X-ray generated by a synchrotron source within the first 72h. The results showed that the addition of C{sub 3}S induces the precipitation of nanosized CDHA at early times depending on the added content. Calculated crystallite sizes showed that the higher the content of C{sub 3}S, the smaller the crystal size at the beginning of the precipitation. These results are different from those obtained by conventional XRD method, suggesting that the proposed technique is a powerful tool in determining the composition and extent of reaction of CPCs surfaces in real time. (author)

  1. Particle size of a new endodontic cement compared to Root MTA and calcium hydroxide

    OpenAIRE

    Soheilipour, Elham; Kheirieh, Sanam; Madani, Majid; Akbarzadeh Baghban, Alireza; Asgary, Saeed

    2009-01-01

    INTRODUCTION: Particle size and distribution can influence the properties of materials. This study analyzed and compared the particle size of Root MTA, calcium hydroxide (CH), and a new endodontic cement called calcium enriched material (CEM). MATERIALS AND METHODS: The particle size of each material was analyzed three times using 0.05 mg of test material with a particle size analyzer. The particle size distribution ranges, the cumulative percentage and the mean of particle sizes were calcula...

  2. Physicochemical properties and biocompatibility of chitosan oligosaccharide/gelatin/calcium phosphate hybrid cements

    International Nuclear Information System (INIS)

    A bone substitute material was developed consisting of a chitosan oligosaccharide (COS) solution in a liquid phase and gelatin (GLT) containing calcium phosphate powder in a solid phase. The physicochemical and biocompatible properties of the hybrid cements were evaluated. The addition of COS to cement did not affect the setting time or diametral tensile strength of the hybrid cements, whereas GLT significantly prolonged the setting time and decreased the strength slightly. The setting reaction was inhibited by the addition of GLT to the initial mixture, but not by COS. However, the presence of GLT appreciably improved the anti-washout properties of the hybrid cement compared with COS. COS may promote the cement's biocompatibility as an approximate twofold increase in cell proliferation for 10% COS-containing cements was observed on day 3 as compared with the controls. The combination of GLT and COS was chosen due to the benefits achieved from several synergistic effects and for their clinical applications. Cement with 5% GLT and 10% COS may be a better choice among cements in terms of anti-washout properties and biological activity.

  3. Immobilisation and solidification of cesium on 11 A calcium silicate hydroxy hydrate column

    International Nuclear Information System (INIS)

    Calcium silicate hydrate closely resembling silicate mineral 11 A tobermorite has been synthesised by hydrothermal treatment of lime and silica at 175 degC. The synthetic mineral exhibits selectivity for Cs+ in the presence of strong solutions of alkali and alkaline earth cations, viz, Na+, K+, Mg2+, Ca2+, Sr2+, etc. The Al-substituted form of this mineral effectively separates cesium ion when used as an exchanger in column of size 35x5 mm (hxr). It is possible to remove 98.65±0.5%Cs+ from a mixed solution of cesium and sodium (0.0001N Cs+ + 0.5N Na+). Column separation of cesium from simulated intermediate level waste solution shows that from the first run ∼ 76% Cs+ can be immobilised on a small column, 18x10mm (hxr), having 2.0 g of exchanger. (author)

  4. 40 CFR 721.10018 - Calcium hydroxide oxide silicate (Ca6(OH)2O2(Si2O5)3).

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Calcium hydroxide oxide silicate (Ca6... New Uses for Specific Chemical Substances § 721.10018 Calcium hydroxide oxide silicate (Ca6(OH)2O2... substance identified as calcium hydroxide oxide silicate (Ca6(OH)2O2(Si2O5)3) (PMN P-01-442; CAS No....

  5. Odontogenic differentiation of human dental pulp cells by calcium silicate materials stimulating via FGFR/ERK signaling pathway

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Chao-Hsin [School of Dentistry, Chung Shan Medical University, Taichung City, Taiwan (China); Hung, Chi-Jr; Huang, Tsui-Hsien [School of Dentistry, Chung Shan Medical University, Taichung City, Taiwan (China); Department of Dentistry, Chung Shan Medical University Hospital, Taichung City, Taiwan (China); Lin, Chi-Chang [Department of Chemical and Materials Engineering, Tunghai University, Taichung City, Taiwan (China); Kao, Chia-Tze [School of Dentistry, Chung Shan Medical University, Taichung City, Taiwan (China); Department of Dentistry, Chung Shan Medical University Hospital, Taichung City, Taiwan (China); Shie, Ming-You, E-mail: eviltacasi@gmail.com [Department of Chemical and Materials Engineering, Tunghai University, Taichung City, Taiwan (China)

    2014-10-01

    Bone healing needs a complex interaction of growth factors that establishes an environment for efficient bone formation. We examine how calcium silicate (CS) and tricalcium phosphate (β-TCP) cements influence the behavior of human dental pulp cells (hDPCs) through fibroblast growth factor receptor (FGFR) and active MAPK pathways, in particular ERK. The hDPCs are cultured with β-TCP and CS, after which the cells' viability and odontogenic differentiation markers are determined by using PrestoBlue® assay and western blot, respectively. The effect of small interfering RNA (siRNA) transfection targeting FGFR was also evaluated. The results showed that CS promoted cell proliferation and enhances FGFR expression. It was also found that CS increases ERK and p38 activity in hDPCs, and furthermore, raises the expression and secretion of DSP, and DMP-1. Additionally, statistically significant differences (p < 0.05) have been found in the calcium deposition in si-FGFR transfection and ERK inhibitor between CS and β-TCP; these variations indicated that ERK/MAPK signaling is involved in the silicon-induced odontogenic differentiation of hDPCs. The current study shows that CS substrates play a key role in odontoblastic differentiation of hDPCs through FGFR and modulate ERK/MAPK activation. - Highlights: • CS influences the behavior of hDPCs through fibroblast growth factor receptor. • CS increases ERK and p38 activity in hDPCs. • ERK/MAPK signaling is involved in the Si-induced odontogenic differentiation of hDPCs. • Ca staining shows that FGFR regulates hDPC differentiation on CS, but not on β-TCP.

  6. Odontogenic differentiation of human dental pulp cells by calcium silicate materials stimulating via FGFR/ERK signaling pathway

    International Nuclear Information System (INIS)

    Bone healing needs a complex interaction of growth factors that establishes an environment for efficient bone formation. We examine how calcium silicate (CS) and tricalcium phosphate (β-TCP) cements influence the behavior of human dental pulp cells (hDPCs) through fibroblast growth factor receptor (FGFR) and active MAPK pathways, in particular ERK. The hDPCs are cultured with β-TCP and CS, after which the cells' viability and odontogenic differentiation markers are determined by using PrestoBlue® assay and western blot, respectively. The effect of small interfering RNA (siRNA) transfection targeting FGFR was also evaluated. The results showed that CS promoted cell proliferation and enhances FGFR expression. It was also found that CS increases ERK and p38 activity in hDPCs, and furthermore, raises the expression and secretion of DSP, and DMP-1. Additionally, statistically significant differences (p < 0.05) have been found in the calcium deposition in si-FGFR transfection and ERK inhibitor between CS and β-TCP; these variations indicated that ERK/MAPK signaling is involved in the silicon-induced odontogenic differentiation of hDPCs. The current study shows that CS substrates play a key role in odontoblastic differentiation of hDPCs through FGFR and modulate ERK/MAPK activation. - Highlights: • CS influences the behavior of hDPCs through fibroblast growth factor receptor. • CS increases ERK and p38 activity in hDPCs. • ERK/MAPK signaling is involved in the Si-induced odontogenic differentiation of hDPCs. • Ca staining shows that FGFR regulates hDPC differentiation on CS, but not on β-TCP

  7. PART II. HYDRATED CEMENTS

    Directory of Open Access Journals (Sweden)

    Milan Drabik

    2014-09-01

    Full Text Available Essential focus of the study has been to acquire thermoanalytical events, incl. enthalpies of decompositions - ΔH, of technological materials based on two types of Portland cements. The values of thermoanalytical events and also ΔH of probes of technological compositions, if related with the data of a choice of minerals of calcium-silicate-sulfate-aluminate hydrates, served as a valued input for the assessment of phases present and phase changes due to the topical hydraulic processes. The results indicate mainly the effects of "standard humidity" or "wet storage" of the entire hydration/hydraulic treatment, but also the presence of cement residues alongside calcium-silicate-sulfate-aluminate hydrates (during the tested period of treatment. "A diluting" effect of unhydrated cement residues upon the values of decomposition enthalpies in the studied multiphase system is postulated and discussed

  8. An ultrasonic through-transmission technique for monitoring the setting of injectable calcium phosphate cement.

    Science.gov (United States)

    Rajzer, Izabella; Piekarczyk, Wojciech; Castaño, Oscar

    2016-10-01

    An ultrasound through-transmission method to monitor the setting process of injectable calcium phosphate bone cements in body fluids is presented. This method can be used to determine the acoustic properties of the bone cement as it sets, which are linked to its material properties and provide some information about changes occurring within the cement. The development of the methodology of ultrasonic testing and execution of velocity measurements of the longitudinal and transverse waves using the through-transmission method made it possible to determine the material constants of samples during the setting and hardening process of an injectable cement paste in physiological fluids (i.e. the Young's modulus (E), the Poisson ratio (ν) and the shear modulus (G)), and to determine the degree of anisotropy of wave velocity in the samples. A strong advantage of the proposed method is that it is non-destructive, and the same sample can be used to monitor the whole process of the cement setting. The testing was performed on premixed and injectable calcium phosphate (CPC)/chitosan blend, where glycerol was used as a liquid phase. Comparisons between ultrasonic velocity and empirical tests such as compressive strength, porosity measurement, FTIR, SEM and XRD analysis at different days of immersion in Ringer's solutions showed that the ultrasonic velocity can be very useful to provide in situ information about changes occurring within the cement. PMID:27287094

  9. Biocompatibility and bioactivity of calcium silicate-based endodontic sealers in human dental pulp cells

    Directory of Open Access Journals (Sweden)

    Leticia Boldrin MESTIERI

    2015-10-01

    Full Text Available Mineral Trioxide Aggregate (MTA is a calcium silicate-based material. New sealers have been developed based on calcium silicate as MTA Fillapex and MTA Plus.Objective The aim of this study was to evaluate biocompatibility and bioactivity of these two calcium silicate-based sealers in culture of human dental pulp cells (hDPCs.Material and Methods The cells were isolated from third molars extracted from a 16-year-old patient. Pulp tissue was sectioned into fragments with approximately 1 mm3 and kept in supplemented medium to obtain hDPCs adherent cultures. Cell characterization assays were performed to prove the osteogenic potential. The evaluated materials were: MTA Plus (MTAP; MTA Fillapex (MTAF and FillCanal (FC. Biocompatibility was evaluated with MTT and Neutral Red (NR assays, after hDPCs exposure for 24 h to different dilutions of each sealer extract (1:2, 1:3 and 1:4. Unexposed cells were the positive control (CT. Bioactivity was assessed by alkaline phosphatase (ALP enzymatic assay in cells exposed for one and three days to sealer extracts (1:4 dilution. All data were analyzed by ANOVA and Tukey post-test (p≤0.05%.Results MTT and NR results showed suitable cell viability rates for MTAP at all dilutions (90-135%. Cells exposed to MTAF and FC (1:2 and 1:4 dilutions showed significant low viability rate when compared to CT in MTT. The NR results demonstrated cell viability for all materials tested. In MTAP group, the cells ALP activity was similar to CT in one and three days of exposure to the material. MTAF and FC groups demonstrated a decrease in ALP activity when compared to CT at both periods of cell exposure.Conclusions The hDPCs were suitable for the evaluation of new endodontic materialsin vitro. MTAP may be considered a promising material for endodontic treatments.

  10. Calcium silicate ceramic scaffolds toughened with hydroxyapatite whiskers for bone tissue engineering

    International Nuclear Information System (INIS)

    Calcium silicate possessed excellent biocompatibility, bioactivity and degradability, while the high brittleness limited its application in load-bearing sites. Hydroxyapatite whiskers ranging from 0 to 30 wt.% were incorporated into the calcium silicate matrix to improve the strength and fracture resistance. Porous scaffolds were fabricated by selective laser sintering. The effects of hydroxyapatite whiskers on the mechanical properties and toughening mechanisms were investigated. The results showed that the scaffolds had a uniform and continuous inner network with the pore size ranging between 0.5 mm and 0.8 mm. The mechanical properties were enhanced with increasing hydroxyapatite whiskers, reached a maximum at 20 wt.% (compressive strength: 27.28 MPa, compressive Young's modulus: 156.2 MPa, flexural strength: 15.64 MPa and fracture toughness: 1.43 MPa·m1/2) and then decreased by addition of more hydroxyapatite whiskers. The improvement of mechanical properties was due to whisker pull-out, crack deflection and crack bridging. Moreover, the degradation rate decreased with the increase of hydroxyapatite whisker content. A layer of bone-like apatite was formed on the scaffold surfaces after being soaked in simulated body fluid. Human osteoblast-like MG-63 cells spread well on the scaffolds and proliferated with increasing culture time. These findings suggested that the calcium silicate scaffolds reinforced with hydroxyapatite whiskers showed great potential for bone regeneration and tissue engineering applications. - Highlights: • HA whiskers were incorporated into CS to improve the properties. • The scaffolds were successfully fabricated by SLS. • Toughening mechanisms was whisker pull-out, crack deflection and bridging. • The scaffolds showed excellent apatite forming ability

  11. Biocompatibility of a new nanomaterial based on calcium silicate implanted in subcutaneous connective tissue of rats

    Directory of Open Access Journals (Sweden)

    Petrović Violeta

    2012-01-01

    Full Text Available The aim of the study was to investigate rat connective tissue response to a new calcium silicate system 7, 15, 30 and 60 days after implantation. Twenty Wistar albino male rats received two tubes half-filled with a new calcium silicate system (NCSS or MTA in subcutaneous tissue. The empty half of the tubes served as controls. Five animals were sacrificed after 7, 15, 30 and 60 days and samples of the subcutaneous tissue around implanted material were submitted to histological analysis. The intensity of inflammation was evaluated based on the number of inflammatory cells present. Statistical analysis was performed using one way ANOVA and Holm Sidak's multiple comparison tests. Mild to moderate inflammatory reaction was observed after 7, 15 and 30 days around a NCSS while mild inflammatory reaction was detected after 60 days of implantation. In the MTA group, mild to moderate inflammatory reaction was found after 7 and 15 days while mild inflammatory reaction was present after 30 and 60 days. There was no statistically significant difference in the intensity of inflammatory reactions between the tested materials and control groups in any experimental period (ANOVA p>0.05. Regarding the intensity of inflammatory reactions at different experimental periods, a statistically significant difference was observed between 7 and 30 days, 7 and 60 days and 15 to 60 days for both materials. For the controls, a statistically significant difference was found between 7 and 60 days and 15 and 60 days of the experiment (Holm Sidak < p 0.001. Subcutaneous tissue of rats showed good tolerance to a new calcium silicate system. Inflammatory reaction was similar to that caused by MTA. [Projekat Ministarstva nauke Republike Srbije, br. 172026

  12. Calcium silicate ceramic scaffolds toughened with hydroxyapatite whiskers for bone tissue engineering

    Energy Technology Data Exchange (ETDEWEB)

    Feng, Pei [State Key Laboratory of High Performance Complex Manufacturing, Central South University, Changsha 410083, PR China, (China); Wei, Pingpin [Cancer Research Institute, Central South University, Changsha 410078 (China); Li, Pengjian; Gao, Chengde [State Key Laboratory of High Performance Complex Manufacturing, Central South University, Changsha 410083, PR China, (China); Shuai, Cijun, E-mail: shuai@csu.edu.cn [State Key Laboratory of High Performance Complex Manufacturing, Central South University, Changsha 410083, PR China, (China); Department of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC 29425 (United States); Peng, Shuping, E-mail: shuping@csu.edu.cn [Cancer Research Institute, Central South University, Changsha 410078 (China)

    2014-11-15

    Calcium silicate possessed excellent biocompatibility, bioactivity and degradability, while the high brittleness limited its application in load-bearing sites. Hydroxyapatite whiskers ranging from 0 to 30 wt.% were incorporated into the calcium silicate matrix to improve the strength and fracture resistance. Porous scaffolds were fabricated by selective laser sintering. The effects of hydroxyapatite whiskers on the mechanical properties and toughening mechanisms were investigated. The results showed that the scaffolds had a uniform and continuous inner network with the pore size ranging between 0.5 mm and 0.8 mm. The mechanical properties were enhanced with increasing hydroxyapatite whiskers, reached a maximum at 20 wt.% (compressive strength: 27.28 MPa, compressive Young's modulus: 156.2 MPa, flexural strength: 15.64 MPa and fracture toughness: 1.43 MPa·m{sup 1/2}) and then decreased by addition of more hydroxyapatite whiskers. The improvement of mechanical properties was due to whisker pull-out, crack deflection and crack bridging. Moreover, the degradation rate decreased with the increase of hydroxyapatite whisker content. A layer of bone-like apatite was formed on the scaffold surfaces after being soaked in simulated body fluid. Human osteoblast-like MG-63 cells spread well on the scaffolds and proliferated with increasing culture time. These findings suggested that the calcium silicate scaffolds reinforced with hydroxyapatite whiskers showed great potential for bone regeneration and tissue engineering applications. - Highlights: • HA whiskers were incorporated into CS to improve the properties. • The scaffolds were successfully fabricated by SLS. • Toughening mechanisms was whisker pull-out, crack deflection and bridging. • The scaffolds showed excellent apatite forming ability.

  13. Novel technique for phosphorus recovery from aqueous solutions using amorphous calcium silicate hydrates (A-CSHs).

    Science.gov (United States)

    Okano, Kenji; Uemoto, Masahide; Kagami, Jumpei; Miura, Keiichi; Aketo, Tsuyoshi; Toda, Masaya; Honda, Kohsuke; Ohtake, Hisao

    2013-05-01

    A novel technique for phosphorus (P) recovery from aqueous solutions was developed using amorphous calcium silicate hydrates (A-CSHs). A-CSHs, which have a high Ca/Si molar ratio of 2.0 or greater, could be synthesized using unlimitedly available, inexpensive materials such as siliceous shale and calcium hydroxide. A-CSHs showed high performance for P recovery from an anaerobic sludge digestion liquor (ASDL) and the synthetic model liquor (s-ASDL) containing 89 mg PO4-P/L. After 20 min mixing, 1.5 g/L A-CSHs could remove approximately 69 and 73% PO4-P from ASDL and s-ASDL, respectively. By contrast, autoclaved lightweight concrete particles, which contained crystalline calcium silicate hydrates as a principal component, removed only 10 and 6% PO4-P from ASDL and s-ASDL, respectively, under the same experimental conditions. When A-CSHs were washed with deionized water to remove free Ca(OH)2, P removability was significantly improved (up to 82%) despite the reduction in the amount of Ca(2+) released. Unlike in the case of Ca(OH)2, no significant carbonate inhibition was observed with P removal by A-CSHs. Moreover, P removed by A-CSHs showed better settleability, filterability, and dewaterability than P precipitated with conventional CaCl2 and Ca(OH)2. The present study demonstrated that A-CSHs have great potential as a novel, beneficial material for P recovery and recycling. PMID:23497975

  14. Mechanical evaluation of implanted calcium phosphate cement incorporated with PLGA microparticles.

    NARCIS (Netherlands)

    Link, D.P.; Dolder, J. van den; Jurgens, W.J.; Wolke, J.G.C.; Jansen, J.A.

    2006-01-01

    In this study, the mechanical properties of an implanted calcium phosphate (CaP) cement incorporated with 20wt% poly (dl-lactic-co-glycolic acid) (PLGA) microparticles were investigated in a rat cranial defect. After 2, 4 and 8 weeks of implantation, implants were evaluated mechanically (push-out te

  15. Preparation and Compressive Strength of Calcium Phosphate Bone Cement Containing N, O-carboxymethyl Chitosan

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    N, O-carboxymethyl chitosan ( CMCTS ), a kind of biodegradable organic substance, was added to calcium phosphate bone cement (CPC) to produce a composite more similar in composition to human bone. The compressive strength of the new material was increased by 10 times compared with conventional CPC.

  16. Bioactive PMMA bone cement prepared by modification with methacryloxypropyltrimethoxysilane and calcium chloride.

    Science.gov (United States)

    Miyazaki, Toshiki; Ohtsuki, Chikara; Kyomoto, Masayuki; Tanihara, Masao; Mori, Akiko; Kuramoto, Kou-ichi

    2003-12-15

    Bone cement consisting of polymethylmethacrylate (PMMA) powder and methylmethacrylate (MMA) liquid is used extensively for fixation of implants such as artificial hip joints with living bone. This type of cement, however, does not show direct bonding to the living body, and hence the fixation is liable to loosen over a long implantation period. Bioactive materials have received much attention because of their capability for bone-bonding, i.e., bioactivity, when implanted in bony defects. Osteoconduction of the bioactive materials is caused by formation of a bone-like apatite layer through a surface reaction between the material and surrounding body fluid. The apatite formation can be induced by a silanol (Sibond;OH) group formed on the materials as well as a dissolution of calcium ion (Ca(2+)) from the material. Incorporation of alkoxysilane and calcium chloride (CaCl(2)) may provide PMMA bone cement with bioactivity, because alkoxysilane gives Sibond;OH after hydrolysis, whereas CaCl(2) releases Ca(2+). In this study, we investigated the potential on bioactivity of the modified PMMA bone cement with alkoxysilane and calcium chloride. PMMA powder was mixed with various amounts of CaCl(2), and MMA liquid with various amounts of 3-methacryloxypropyltrimethoxysilane (MPS). The mixed paste was immersed in a simulated body fluid (Kokubo solution) that has a similar concentration in inorganic constituents to human blood plasma. After soaking for various periods, apatite formation on the cement was examined. Apatite formation was observed by the addition of CaCl(2) with contents of 16 mass % and more. Incorporation of MPS accelerates the apatite formation. Setting time of the cement was significantly elongated after the addition of MPS, whereas compressive strength significantly decreased with increasing the contents of CaCl(2) and MPS. The hardened cement containing 20 mass % of CaCl(2) in the powder and 20 mass % of MPS in the liquid showed a tendency to be more

  17. Specific interaction of cesium with the surface of calcium silicate hydrates

    International Nuclear Information System (INIS)

    The sorption of cesium at the calcium silicate hydrates (CSH) surface was investigated, both through sorption isotherm data and by solid-state NMR experiments. The sorption ability of CSH towards cesium is favored for low solid Ca/Si molar ratios, in agreement with the negative surface charge they develop then. A significant proportion of these sorbed cesium cations remains tightly bound to the surface sites forming, in dehydrated CSH, inner-sphere complexes, which can not be removed by alcohol washing. Chloride seems to present a lower affinity for CSH, even for high Ca/Si molar ratios, where the surface charge becomes positive. (orig.)

  18. Sorption study of 137Cs on Al-substituted calcium silicate hydroxy hydrate

    International Nuclear Information System (INIS)

    Calcium silicate hydroxy hydrate is also known as tobermorite and it is similar to Ca5AlxSi6-xO18H24.nH2O (where x = 0.025) in composition. Sorption studies have been investigated by radiometric technique at room temperature. The 137Cs selectivity has been examined in presence of 1000 times concentrated solution of Na+, Ca2+ and Ba2+. The data suggests that tobermorite could be used for immobilisation of radioactive caesium. (author)

  19. The Performance of Calcium Silicate Board Partition Fireproof Drywall Assembly with Junction Box under Fire

    OpenAIRE

    Yinuo Wang; Ying-Ji Chuang; Ching-Yuan Lin

    2015-01-01

    This study uses a metal stud partition fireproof drywall measuring 83 mm in thickness as a test specimen to explore the impact of an embedded junction box on the firefighting performance of the wall through one time of standard fire test on a 300 cm × 300 cm area and five times of standard fire test on a 120 cm × 120 cm area. The results show that the quality of calcium silicate board plays a big role in the fireproof effectiveness. The embedded junction box located on the backside of the f...

  20. Evaluation of antibacterial and antifungal activity of new calcium-based cement (Biodentine) compared to MTA and glass ionomer cement

    Science.gov (United States)

    Bhavana, Vankayala; Chaitanya, Krishna Popuri; Gandi, Padma; Patil, Jayaprakash; Dola, Binoy; Reddy, Rahul B.

    2015-01-01

    Objective: To evaluate the antibacterial and antifungal properties of calcium-based cement, Biodentine (Ca3SiO2), compared to commercial glass ionomer cements (GICs) and mineral trioxide aggregate (MTA). Materials and Methods: Pellets of GICs, ProRoot MTA, and Biodentine were prepared to test the influence of these cements on the growth of four oral microbial strains: Streptococcus mutans, Enterococcus faecalis, Escherichia coli, and Candida albicans; using agar diffusion method. Wells were formed by removing the agar and the manipulated materials were immediately placed in the wells. The pellets were lodged in seeded plates and the growth inhibition diameter around the material was measured after 24-72 h incubation at 37°C. The data were analyzed using analysis of variance (ANOVA) test to compare the differences among the three cements at different concentrations. Results: Test indicates that the antimicrobial activity of Biodentine, on all the microorganisms tested, was very strong, showing a mean inhibition zone of 3.2 mm, which extends over time towards all the strains. For Biodentine, GIC, and MTA, the diameters of the inhibition zones for S. mutans were significantly larger than for E. faecalis, Candida, and E. coli (P Biodentine created larger inhibition zones than MTA and GIC. PMID:25657526

  1. Evaluation of antibacterial and antifungal activity of new calcium-based cement (Biodentine compared to MTA and glass ionomer cement

    Directory of Open Access Journals (Sweden)

    Vankayala Bhavana

    2015-01-01

    Full Text Available Objective: To evaluate the antibacterial and antifungal properties of calcium-based cement, Biodentine (Ca 3 SiO 2 , compared to commercial glass ionomer cements (GICs and mineral trioxide aggregate (MTA. Materials and Methods: Pellets of GICs, ProRoot MTA, and Biodentine were prepared to test the influence of these cements on the growth of four oral microbial strains: Streptococcus mutans, Enterococcus faecalis, Escherichia coli, and Candida albicans; using agar diffusion method. Wells were formed by removing the agar and the manipulated materials were immediately placed in the wells. The pellets were lodged in seeded plates and the growth inhibition diameter around the material was measured after 24-72 h incubation at 37°C. The data were analyzed using analysis of variance (ANOVA test to compare the differences among the three cements at different concentrations. Results: Test indicates that the antimicrobial activity of Biodentine, on all the microorganisms tested, was very strong, showing a mean inhibition zone of 3.2 mm, which extends over time towards all the strains. For Biodentine, GIC, and MTA, the diameters of the inhibition zones for S. mutans were significantly larger than for E. faecalis, Candida, and E. coli (P < 0.05. Conclusion: All materials showed antimicrobial activity against the tested strains except for GIC on Candida. Largest inhibition zone was observed for Streptococcus group. Biodentine created larger inhibition zones than MTA and GIC.

  2. Stabilization of ZnCl2-containing wastes using calcium sulfoaluminate cement: cement hydration, strength development and volume stability.

    Science.gov (United States)

    Berger, Stéphane; Cau Dit Coumes, Céline; Le Bescop, Patrick; Damidot, Denis

    2011-10-30

    The potential of calcium sulfoaluminate (CSA) cement was investigated to solidify and stabilize wastes containing large amounts of soluble zinc chloride (a strong inhibitor of Portland cement hydration). Hydration of pastes and mortars prepared with a 0.5 mol/L ZnCl(2) mixing solution was characterized over one year as a function of the gypsum content of the binder and the thermal history of the material. Blending the CSA clinker with 20% gypsum enabled its rapid hydration, with only very small delay compared with a reference prepared with pure water. It also improved the compressive strength of the hardened material and significantly reduced its expansion under wet curing. Moreover, the hydrates assemblage was less affected by a thermal treatment at early age simulating the temperature rise and fall occurring in a large-volume drum of cemented waste. Fully hydrated materials contained ettringite, amorphous aluminum hydroxide, strätlingite, together with AFm phases (Kuzel's salt associated with monosulfoaluminate or Friedel's salt depending on the gypsum content of the binder), and possibly C-(A)-S-H. Zinc was readily insolubilized and could not be detected in the pore solution extracted from cement pastes. PMID:21889260

  3. Simple preparation and initial characterization of semi-amorphous hollow calcium silicate hydrate nanoparticles by ammonia-hydrothermal-template techniques

    International Nuclear Information System (INIS)

    Semi-amorphous hollow calcium silicate hydrate nanoparticles (CS10d120Hac) were successfully synthesized via simple ammonia-hydrothermal-template approach (AHT) followed by acid treatment. Results revealed that the newly synthesized samples had homogenous hollow nano-interior wherein the shell wall contained semi-amorphous calcium silicate hydrate. The AHT intensified the formation of a stronger electrostatic interaction (Si–O–Ca) from the weaker electrostatic contact composed of silicate wall-calcium hydroxide interaction (Si–OH–Ca) forming a thin semi-amorphous calcium silicate hydrate shell wall. This is also a convenient way for structural stability of the hollow CS10d120Hac. The CS10d120Hac showed a relatively higher surface area, which is uniquely rare especially if compared with bulk calcium silicate particles. This CS10d120Hac can be selectively functionalized with multiple organic and inorganic groups. Hence, this work may open a new route for the formation of hybrid hollow bio-active particles.

  4. Fluorescent properties of a blue-to green-emitting Ce3+, Tb3+ codoped amorphous calcium silicate phosphors

    International Nuclear Information System (INIS)

    Ce3+, Tb3+ codoped amorphous calcium silicate phosphor was prepared by heating (830 °C for 30 min) Ce3+, Tb3+ codoped calcium silicate hydrate phosphor formed by liquid-phase reaction. The excitation peak wavelength of the resulting phosphor was 330 nm and the emission peak wavelengths were at 544 nm, attributed to the 5D4→7F5 transition of Tb3+, and at 430–470 mm, attributed to Ce3+. The intensity ratio of the two peaks could be freely controlled by varying the Tb/Ca atomic ratio of the Ce3+, Tb3+ codoped amorphous calcium silicate phosphor, allowing light to be emitted over a wide range from blue to green. It was clarified that energy transfer exists from Ce3+ to Tb3+. - Graphical abstract: Ce3+, Tb3+ codoped calcium silicate hydrate phosphor was synthesized by liquid-phase reaction. This was heated at 830 °C to obtain a Ce3+, Tb3+ codoped amorphous calcium silicate phosphor. Under 330 nm excitation, this phosphor showed emission peaks at 430–470 nm and 542 nm. The luminescent color could be continuously changed blue to green with increasing Tb/Ca atomic ratio. It was clarified that electron transfer from Ce3+ to Tb3+ is occurring.

  5. Influence of sodium borate on the early age hydration of calcium sulfoaluminate cement

    International Nuclear Information System (INIS)

    Calcium sulfoaluminate (CSA) cements are potential candidates for the conditioning of radioactive wastes with high sodium borate concentrations. This work thus investigates early age hydration of two CSA cements with different gypsum contents (0 to 20%) as a function of the mixing solution composition (borate and NaOH concentrations). Gypsum plays a key role in controlling the reactivity of cement. When the mixing solution is pure water, increasing the gypsum concentration accelerates cement hydration. However, the reverse is observed when the mixing solution contains sodium borate. Until gypsum exhaustion, the pore solution pH remains constant at ~ 10.8, and a poorly crystallized borate compound (ulexite) precipitates. A correlation is established between this transient precipitation and the hydration delay. Decreasing the gypsum content in the binder, or increasing the sodium content in the mixing solution, are two ways of reducing the stability of ulexite, thus decreasing the hydration delay

  6. Influence of sodium borate on the early age hydration of calcium sulfoaluminate cement

    Energy Technology Data Exchange (ETDEWEB)

    Champenois, Jean-Baptiste; Dhoury, Mélanie [CEA, DEN, DTCD, SPDE, F-30207 Bagnols-sur-Cèze Cedex (France); Cau Dit Coumes, Céline, E-mail: celine.cau-dit-coumes@cea.fr [CEA, DEN, DTCD, SPDE, F-30207 Bagnols-sur-Cèze Cedex (France); Mercier, Cyrille [LMCPA, Université de Valenciennes et du Hainaut Cambrésis, 59600 Maubeuge (France); Revel, Bertrand [Centre Commun de Mesure RMN, Université Lille1 Sciences Technologies, Cité Scientifique, 59655 Villeneuve d' Ascq Cedex (France); Le Bescop, Patrick [CEA, DEN, DPC, SECR, F-91192 Gif-sur-Yvette (France); Damidot, Denis [Ecole des Mines de Douai, LGCgE-GCE, 59508 Douai (France)

    2015-04-15

    Calcium sulfoaluminate (CSA) cements are potential candidates for the conditioning of radioactive wastes with high sodium borate concentrations. This work thus investigates early age hydration of two CSA cements with different gypsum contents (0 to 20%) as a function of the mixing solution composition (borate and NaOH concentrations). Gypsum plays a key role in controlling the reactivity of cement. When the mixing solution is pure water, increasing the gypsum concentration accelerates cement hydration. However, the reverse is observed when the mixing solution contains sodium borate. Until gypsum exhaustion, the pore solution pH remains constant at ~ 10.8, and a poorly crystallized borate compound (ulexite) precipitates. A correlation is established between this transient precipitation and the hydration delay. Decreasing the gypsum content in the binder, or increasing the sodium content in the mixing solution, are two ways of reducing the stability of ulexite, thus decreasing the hydration delay.

  7. X-ray diffraction: a powerful tool to probe and understand the structure of nanocrystalline calcium silicate hydrates

    International Nuclear Information System (INIS)

    The structure of nanocrystalline calcium silicate hydrates (C-S-H) was studied using X-ray diffraction and literature data. It is proposed that C-S-H of Ca/Si ratio ranging between ∼ 0.6 and ∼ 1.7 can be described as nanocrystalline tobermorite affected by turbostratic disorder. The broadening and shift of the basal reflection positioned between ∼ 13.5 and ∼ 11.2 Å (depending on the Ca/Si ratio) arises from nanocrystallinity and possibly from an interstratification phenomenon. X-ray diffraction (XRD) patterns were calculated and compared to literature data with the aim of investigating the crystal structure of nanocrystalline calcium silicate hydrates (C-S-H), the main binding phase in hydrated Portland cement pastes. Published XRD patterns from C-S-H of Ca/Si ratios ranging from ∼ 0.6 to ∼ 1.7 are fully compatible with nanocrystalline and turbostratic tobermorite. Even at a ratio close or slightly higher than that of jennite (Ca/Si = 1.5) this latter mineral, which is required in some models to describe the structure of C-S-H, is not detected in the experimental XRD patterns. The 001 basal reflection from C-S-H, positioned at ∼ 13.5 Å when the C-S-H structural Ca/Si ratio is low (< 0.9), shifts towards smaller d values and sharpens with increasing Ca/Si ratio, to reach ∼ 11.2 Å when the Ca/Si ratio is higher than 1.5. Calculations indicate that the sharpening of the 001 reflection may be related to a crystallite size along c* (i.e. a mean number of stacked layers) increasing with the C-S-H Ca/Si ratio. Such an increase would contribute to the observed shift of the 001 reflection, but fails to quantitatively explain it. It is proposed that the observed shift could result from interstratification of at least two tobermorite-like layers, one having a high and the other a low Ca/Si ratio with a basal spacing of 11.3 and 14 Å, respectively

  8. Synthesis and characterization of calcium-alumino-silicate hydrates from oil shale ash - Towards industrial applications

    Energy Technology Data Exchange (ETDEWEB)

    Janek Reinik; Ivo Heinmaa; Jyri-Pekka Mikkola; Uuve Kirso [National Institute of Chemical Physics and Biophysics, Tallinn (Estonia)

    2008-08-15

    The influence of the alkaline medium on the hydrothermal activation of the oil shale fly ash with NaOH and KOH was studied using SEM/EDX, XRD, {sup 29}Si and {sup 27}Al high-resolution MAS-NMR spectra. In the presence of NaOH the silicon in the original fly ash was completely converted into calcium-aluminum-silicate-hydrates, mainly into 1.1 nm tobermorite structure during 24-h treatment at 160{sup o}C. At similar reaction conditions, the activation with KOH resulted only to the formation of amorphous calcium-silica-hydrate gel on the surface of ash particles at temperature. The results obtained in this study indicate that the oil shale fly ash can be used for production of Al-substituted tobermorites when strongly alkaline media (NaOH) is applied. The synthesized product was used in a catalytic d-lactose isomerization reaction. 29 refs., 7 figs., 2 tabs.

  9. CITRIC ACID AS A SET RETARDER FOR CALCIUM ALUMINATE PHOSPHATE CEMENTS.

    Energy Technology Data Exchange (ETDEWEB)

    SUGAMA,T.; BROTHERS, L.E.

    2005-01-01

    Citric acid added as set retarder significantly contributed to enhancing the setting temperature and to extending the thickening time of a calcium aluminate phosphate (CaP) geothermal cement slurry consisting of calcium aluminate cement (CAC) as the base reactant and sodium polyphosphate (NaP) solution as the acid reactant. The set-retarding activity of citric acid was due to the uptake of Ca{sup 2+} ions from the CAC by carboxylic acid groups within the citric acid. This uptake led to the precipitation of a Ca-complexed carboxylate compound as a set-retarding barrier layer on the CAC grains' surfaces. However, this barrier layer was vulnerable to disintegration by the attack of free Ca{sup 2+} ions from CAC, and also to degradation at elevated temperature, thereby promoting the generation of exothermic energy from acid-base reactions between the CAC and NaP after the barrier was broken. The exothermic reaction energy that was promoted in this way minimized the loss in strength of the citric acid-retarded cement. The phase composition assembled in both retarded and non-retarded cements after autoclaving at 180 C encompassed three reaction products, hydroxyapatite (HOAp), hydrogrossular and boehmite, which are responsible for strengthening the autoclaved cement. The first two reaction products were susceptible to reactions with sulfuric acid and sodium sulfate to form crystalline bassanite scale as the corrosion product. The boehmite phase possessed a great resistance to acid and sulfate. Although the bassanite scales clinging to the cement's surfaces were the major factor governing the loss in weight, they served in protecting the cement from further acid- and sulfate-corrosion until their spallation eventually occurred. Nevertheless, the repetitive processes of HOAp and hydrogrossular {yields} bassanite {yields} spallation played an important role in extending the useful lifetime of CaP cement in a low pH environment at 180 C.

  10. The Mechanical Properties and Hydration Characteristics of Cement Pastes Containing Added-calcium Coal Gangue

    Institute of Scientific and Technical Information of China (English)

    LI Dongxu; SONG Xuyan

    2008-01-01

    The mechanical properties of several kinds of coal gangue calcined with limestone were Researched so as to find the optimum way of calcinations with limestone. Mierostructure and property of hydration process of cement pastes containing added-calcium coal gangue were analyzed by means of scanning electron microscope (SEM) and method of mercury in trusion poremeasurement (MIP), etc. The experiment can approve those results: when proper amounst of gypsum and fluorite were taken as mineralizers in the course of calcinations of added-calcium coal gangue, activity of coal gangue can be effectively improved. The results of mechanical property and structural characteristic such as hydration process, hydration product and microstructure etc. of cement pastes containing added-calcium coal gangue are consistent.

  11. The mechanical properties and hydration characteristics of cement pastes containing added-calcium coal gangue

    Energy Technology Data Exchange (ETDEWEB)

    Dongxu Li; Xuyan Song [Nanjing University of Technology, Nanjing (China). College of Material Science and Engineering

    2008-04-15

    The mechanical properties of several kinds of coal gangue calcined with limestone were researched so as to find the optimum way of calcinations with limestone. The microstructure and property of hydration process of cement pastes containing added-calcium coal gangue were analyzed by means of scanning electron microscope (SEM) and the method of mercury in trusion poremeasurement. When the proper amounst of gypsum and fluorite were taken as mineralizers in the course of calcinations of added-calcium coal gangue, the activity of coal gangue can be effectively improved. The results of mechanical property and structural characteristics such as hydration, hydration products and microstructure etc. of cement pastes containing added-calcium coal gangue are consistent.

  12. Early-age hydration and volume change of calcium sulfoaluminate cement-based binders

    Science.gov (United States)

    Chaunsali, Piyush

    Shrinkage cracking is a predominant deterioration mechanism in structures with high surface-to-volume ratio. One way to allay shrinkage-induced stresses is to use calcium sulfoaluminate (CSA) cement whose early-age expansion in restrained condition induces compressive stress that can be utilized to counter the tensile stresses due to shrinkage. In addition to enhancing the resistance against shrinkage cracking, CSA cement also has lower carbon footprint than that of Portland cement. This dissertation aims at improving the understanding of early-age volume change of CSA cement-based binders. For the first time, interaction between mineral admixtures (Class F fly ash, Class C fly ash, and silica fume) and OPC-CSA binder was studied. Various physico-chemical factors such as the hydration of ye'elimite (main component in CSA cement), amount of ettringite (the main phase responsible for expansion in CSA cement), supersaturation with respect to ettringite in cement pore solution, total pore volume, and material stiffness were monitored to examine early-age expansion characteristics. This research validated the crystallization stress theory by showing the presence of higher supersaturation level of ettringite, and therefore, higher crystallization stress in CSA cement-based binders. Supersaturation with respect to ettringite was found to increase with CSA dosage and external supply of gypsum. Mineral admixtures (MA) altered the expansion characteristics in OPC-CSA-MA binders with fixed CSA cement. This study reports that fly ash (FA) behaves differently depending on its phase composition. The Class C FA-based binder (OPC-CSA-CFA) ceased expanding beyond two days unlike other OPC-CSA-MA binders. Three factors were found to govern expansion of CSA cement-based binders: 1) volume fraction of ettringite in given pore volume, 2) saturation level of ettringite, and 3) dynamic modulus. Various models were utilized to estimate the macroscopic tensile stress in CSA cement

  13. Hydration studies of calcium sulfoaluminate cements blended with fly ash

    OpenAIRE

    Garcia-Maté, Marta; De la Torre, Angeles G; León-Reina, Laura; Aranda, Miguel A. G.; Santacruz, Isabel

    2013-01-01

    The main objective of this work is to study the hydration and properties of calciumsulfoaluminate cement pastes blended with fly ash (FA) and the corresponding mortars at different hydration ages. Laboratory X-ray powder diffraction, rheological studies, thermal analysis, porosimetry and compressive strength measurements were performed. The analysis of the diffraction data by Rietveld method allowed quantifying crystalline phases and overall amorphous contents. The studied paramet...

  14. Development of a fully injectable calcium phosphate cement for orthopedic and dental applications

    Indian Academy of Sciences (India)

    Manoj Komath; H K Varma

    2003-06-01

    A study on the development of a fully injectable calcium phosphate cement for orthopedic and dental applications is presented. The paper describes its characteristic properties including results of bio- compatibility studies. A conventional two-component calcium phosphate cement formulation (having a powder part containing dry mixture of acidic and basic calcium phosphate particles and a liquid part containing phosphate solution) is modified with a biocompatible gelling agent, to induce flow properties and cohesion. The quantity of the gelling agent is optimized to get a viscous paste, which is smoothly injectable through an 18-gauge needle, with clinically relevant setting parameters. The new formulation has a setting time of 20 min and a compressive strength of 11 MPa. The X-ray diffraction, Fourier transform infrared spectrometry, and energy dispersive electron microprobe analyses showed the phase to be hydroxyapatite, the basic bone mineral. Scanning electron microscopy revealed a porous structure with particle sizes of a few micrometers. The cement did not show any appreciable dimensional or thermal change during setting. The injectability is estimated by extruding through needle and the cohesive property is assessed by water contact method. The cement passed the in vitro biocompatibility screening (cytotoxicity and haemolysis) tests.

  15. An experimental approach to the study of the rheology behaviour of synthetic bone calcium phosphate cements

    Energy Technology Data Exchange (ETDEWEB)

    Friberg, J.; Fernandez, E.; Sarda, S.; Nilsson, M.; Ginebra, M.P.; Planell, J.A. [Universidad Politecnica de Catalunya, Barcelona (Spain). Dept. of Materials Science and Metallurgical Engineering; Martinez, S. [Barcelona Univ. (Spain). Mineralogia i Recursos Minerals

    2001-07-01

    Calcium phosphate cements were developed to fit surgical needs in biomedical fields such as odontology or traumatology. Nowadays, a broad field of new applications have been found for this kind of materials. Drug delivery systems, tissue-engineering scaffolds and osteoporotic bone filling applications are some of the new fields that are being benefited with these materials. Looking at both, commercial and new experimental calcium phosphate cements it is found that {alpha}-tricalcium phosphate is the main reactive powder responsible for the setting and the hardening of the cement. Thus, it is important to know how {alpha}-tricalcium phosphate affects injectability of these cements. The aim of this study was to investigate the rheological behaviour of {alpha}-tricalcium phosphate slurries in order to know how the cement injectability should be modified. Factors such as liquid to powder ratio, particle size of the main reactive powder and the addition of dispersants have been considered. The results showed that viscosity decreased when particle size of reactant was increased and when liquid to powder ratio was increased. It was also found that a minimum of viscosity exists at an optimum value of the weight percentage of dispersant. (orig.)

  16. Characterization of cement calcium phosphate for use dental

    International Nuclear Information System (INIS)

    Calcium phosphates are interesting biological and medical attention due to its occurrence in different animal species and humans. Ceramics based on calcium phosphate in the form of implants or porous particulate materials, have proven to be suitable replacements for bone tissue when they are only subjected to small mechanical stresses. Was obtained research laboratory DEMA/UFCG a calcium phosphate phase. The goal is to characterize the material by X-ray diffraction (XRD) in order to analyze what the phases and infrared spectroscopy (FTIR) to identify the absorption bands of the bonding characteristic. Was identified by XRD phase present in the sample is hydroxyapatite Ca/P 1.67. In infrared spectroscopy has absorption bands characteristic of the phosphate group at 1032 cm1 region. (author)

  17. Calcium sulfoaluminate cement blended with OPC: A potential binder to encapsulate low-level radioactive slurries of complex chemistry

    International Nuclear Information System (INIS)

    Investigations were carried out in order to solidify in cement a low-level radioactive waste of complex chemistry obtained by mixing two process streams, a slurry produced by ultra-filtration and an evaporator concentrate with a salinity of 600 gxL-1. Direct cementation with Portland cement (OPC) was not possible due to a very long setting time of cement resulting from borates and phosphates contained in the waste. According to a classical approach, this difficulty could be solved by pre-treating the waste to reduce adverse cement-waste interactions. A two-stage process was defined, including precipitation of phosphates and sulfates at 60 deg. C by adding calcium and barium hydroxide to the waste stream, and encapsulation with a blend of OPC and calcium aluminate cement (CAC) to convert borates into calcium quadriboroaluminate. The material obtained with a 30% waste loading complied with specifications. However, the pre-treatment step made the process complex and costly. A new alternative was then developed: the direct encapsulation of the waste with a blend of OPC and calcium sulfoaluminate cement (CSA) at room temperature. Setting inhibition was suppressed, which probably resulted from the fact that, when hydrating, CSA cement formed significant amounts of ettringite and calcium monosulfoaluminate hydrate which incorporated borates into their structure. As a consequence, the waste loading could be increased to 56% while keeping acceptable properties at the laboratory scale.

  18. Bond strength of a calcium silicate-based sealer tested in bulk or with different main core materials

    OpenAIRE

    Nagas, Emre; Cehreli, Zafer; Mehmet Ozgur UYANIK; Veli DURMAZ

    2014-01-01

    The aim of this study was to evaluate the influence of a calcium silicate-based sealer (iRoot SP), with or without a core material, on bond strength to radicular dentin, in comparison with various contemporary root filling systems. Root canals of freshly extracted single-rooted teeth (n = 60) were instrumented using rotary instruments. The roots were randomly assigned to one of the following experimental groups: (1) a calcium silicate-based sealer without a core material (bulk-fill); (2) a ca...

  19. Effect of temperature on the microstructure of calcium silicate hydrate (C-S-H)

    International Nuclear Information System (INIS)

    Temperature affects the properties of concrete through its effect on the hydration of cement and its associated microstructural development. This paper focuses on the modifications to C-S-H induced by isothermal curing between 5 and 60 °C. The results show that as the temperature increases (within the range studied) the C/S ratio of C-S-H changes only slightly, with a higher degree of polymerisation of silicate chains, but there is a significant decrease in its bound water content and an increase of apparent density of 25%. This increase seems to come from a different packing of C-S-H at the nanoscale. As a consequence of these changes, the microstructure of the cement paste is much coarser and porous, which explains the lower final strengths obtained by curing at elevated temperatures. -- Highlights: •C-S-H structure studied at the atomic level •Multiple analytical techniques used •Studies conducted at temperatures above and below normal temperatures

  20. Clogging and Cementation Caused by Calcium or Iron Biogrouts

    Science.gov (United States)

    Ivanov, V.; Chu, J.; Naeimi, M.

    2012-12-01

    Chemical grouts are often used to reduce the hydraulic conductivity of soil for seepage control purposes. However, chemical grouts can be expensive and environmentally unfriendly. Therefore, two new biogrouts were tested for their bioclogging and biocementation properties. The first was calcium-based biogrout, which contained urease-producing bacteria, calcium chloride and urea for the crystallization of calcite due to enzymatic hydrolysis of urea. The second was iron-based biogrout, which consisted of urease-producing bacteria, ferric chelate, and urea for the precipitation of ferric hydroxide and carbonate due to enzymatic hydrolysis of urea. The permeability of sand (P, 10^-5 m/s), treated with calcium-based biogrout, linearly decreased as a function of the content of precipitated calcium (C, % w/w) according to the following equation: P = 5.1 - 4.0 C. Meanwhile, the permeability of sand treated with iron-based biogrout dropped to 2.7x10^-6 m/s at content of precipitated iron (F, % w/w) about 0.35 % w/w , by the equation: P = 5.1 - 14.6 F , and then slowly decreased to 1.4x10^-7 m/s at content of precipitated iron 1.8% w/w by the following equation: P = 0.36 - 0.23F. Both biogrouts have approximately same efficiency in the reduction of permeability of sand to low values. However, the mechanisms of bioclogging are probably different because the reduction of permeability by calcium-based biogrout was described by linear function of precipitated calcium but the reduction of permeability by iron-based biogrout showed two steps of the clogging. Different functions and mechanisms were related probably to the different type of precipitates. The images of biogrouted sand samples show that calcium-based biogrout produced white amorphous or crystallised calcium carbonate, while iron-based biogrout produced gel-like brown precipitate without visible crystals. The unconfined compressive strengths of the sand treated with different biogrouts (Y, kPa) increased by power

  1. Influence of the use of nanoscale siliceous cement system on the strength

    OpenAIRE

    KOSACH Anatoliy Fyodorovich; DANILOV Sergey Valeryevich; GUTAREVA Natalya Anatolyevna; KOROTAEV Maksim Aleksandrovich

    2014-01-01

    The article is devoted to creation of scientific basis for cement stone structure formation, development of optimal compositions and technology for manufacturing building materials based on the waste of fine-grained pure quartz production. This technology provides significant pore filling, formation of new crystallization centers which act as an dditional reinforcement of cement hydration products, and increase of physical and mechanical properties.

  2. Monitoring of hardening and hygroscopic induced strains in a calcium phosphate bone cement using FBG sensor.

    Science.gov (United States)

    Bimis, A; Karalekas, D; Bouropoulos, N; Mouzakis, D; Zaoutsos, S

    2016-07-01

    This study initially deals with the investigation of the induced strains during hardening stage of a self-setting calcium phosphate bone cement using fiber-Bragg grating (FBG) optical sensors. A complementary Scanning Electron Microscopy (SEM) investigation was also conducted at different time intervals of the hardening period and its findings were related to the FBG recordings. From the obtained results, it is demonstrated that the FBG response is affected by the microstructural changes taking place when the bone cement is immersed into the hardening liquid media. Subsequently, the FBG sensor was used to monitor the absorption process and hygroscopic response of the hardened and dried biocement when exposed to a liquid/humid environment. From the FBG-based calculated hygric strains as a function of moisture concentration, the coefficient of moisture expansion (CME) of the examined bone cement was obtained, exhibiting two distinct linear regions. PMID:26807773

  3. Biomechanical evaluation of vertebroplasty using calcium sulfate cement for thoracolumbar burst fractures

    Institute of Scientific and Technical Information of China (English)

    WU Xiao-tao; JIANG Xing-jie; ZHANG Shao-dong; YANG Hui-lin

    2007-01-01

    Objective: To evaluate the biomechanical performance of vertebroplasty using calcium sulfate cement for thoracolumbar burst fractures.Methods: Sixteen bovine thoracolumbar spines (T11-L1 ) were divided into 4 groups (A, B, C and D). After burst-fracture model was created, 12 vertebral bodies in Groups A, B and C were augmented with calcium sulfate cement (CSC), calcium phosphate cement (CPC) and polymethylmethacrylate ( PMMA ) bone cement,respectively. Each anterior vertebral body height was measured with a caliper at 4 time points: intact conditions(HInt), post-fracture (HFr), post-reduction (HRe) and post-vertebroplasty (HVP). The filling volume of 3 different bone cements was also measured. Each vertebral body was compressed at 0.5 mm/s using a hinged plating system on a materials testing machine to 50% of the postvertebroplasty height to determine strength and stiffness.Difference was checked using t test or One-way ANOVA.Results: The average strike energy was 66. 2 J.Vertebroplasty with different cements could sustain vertebral height. The average filling volume of bone cement in 3 groups was 4.35 ml (CSC), 3.72 ml (CPC) and 3.95 ml (PMMA), respectively, and there was no statistically significant difference among them ( P >0.05).Vertebroplasty with PMMA completely restored strength(116%) and stiffness (105%). CSC or CPC partly recovered vertebral strength and stiffness. However,greater strength restoration was got with CSC ( 1 659 N) as compared with CPC (1 011N, P<0.01 ). Regarding stiffness, differences between CSC (140 N/mm ±40 N/mm)and the other two bone cements ( CPC :148 N/mm ±33 N/mm,PMMA:236 N/mm ±97 N/mm) were not significant (P>0.05).Conclusions: For a burst-fracture of calf spine, useof CSC for vertebroplasty yields similar vertebral stiffnessas compared with PMMA or CPC. Although augmentationwith CSC partly obtains the normal strength, thistreatment still can be applied in thoracolumbar burstfractures with other instrumental devices in

  4. In-situ observation on the transformation of calcium phosphate cement into hydroxyapatite

    International Nuclear Information System (INIS)

    In the present study, the in-situ transformation of calcium phosphate cement into hydroxyapatite (HAp) within the first hour is monitored with a synchrotron X-ray beam. A disodium hydrogen phosphate solution is used as cement liquid to activate the reaction between dicalcium phosphate anhydrous (DCPA) and calcium hydroxide (Ca(OH)2). The XRD analysis indicates that the amounts of DCPA and Ca(OH)2 first decrease within the first min of the reaction. Then, the intensity of DCPA's XRD peaks starts to increase instead in the period of 5 to 20 min. After 20 min, the DCPA particles are consumed slowly to form fine HAp particles. Large pores are evident upon the completion of reaction.

  5. Solid-state P-31 MR studies of bone mineral and calcium phosphate bone cements

    International Nuclear Information System (INIS)

    Calcium phosphate bone cements have recently been used to promote bone healing and remodeling, but little is known of their bioabsorption. The purpose of this paper to characterize and quantitate bone mineral and calcium phosphate bone cements with the use of solid-state P-31 NMR imaging to establish a model for bioabsorption studies. Pulverized cortical rabbit bone, octacalcium phosphate spherulites, and two synthetic apatite formulations (A and B, Norian, Mountain View, Calif) were evaluated in vitro. A 9.4-T Varian VXR-400S spectrometer operating at 161.9 MHz for P-31 was used to obtain NMR imaging spectra with the magic-angel spinning technique at a sample spin frequency of 6-7.5 kHz, utilizing an external 85% phosphoric acid reference. T1 was determined in a static 90 degrees τ 90 degrees experiment. Quantitation was attempted in mixed samples

  6. Conditioning highly concentrated borate solutions with calcium sulfo-aluminate cement

    International Nuclear Information System (INIS)

    The early age hydration by borate solution of 3 calcium sulfo-aluminate cements (CSA), containing respectively 0%, 10% and 20% of gypsum by weight of cement was studied using isothermal calorimetry and dynamic mode rheo-metry. XRD and TGA analysis were carried out on pastes with increasing hydration degrees (up to 90 days) to specify the mineralogy and to figure out the mechanisms of borate immobilisation. It has been shown that the retarding effect of borate anions is due to the precipitation of the amorphous calcium borate C2B3H8; borate anions were then incorporated in Aft-type phases. The macroscopic properties of hydrated binders (compressive strength, length change) were also followed during 180 days. It appears that the mechanical strength continuously increases with the hydration degree. Length changes under wet-curing and sealed bag remain moderate and seem to be stabilized after 180 days

  7. Calcium phosphate holmium-166 ceramic to addition in bone cement: synthesis and characterization

    International Nuclear Information System (INIS)

    Spine metastases are a common and painful complication of cancer. The treatment often consists of bone cement injection (vertebroplasty or kyphoplasty) within vertebral body for vertebrae stabilization, followed by external beam radiation therapy. Recently, researchers introduced the concept of radioactive bone cement for spine tumors therapy. Then, investigations about bioactive and radioactive materials became interesting. In this study, we present the synthesis of calcium phosphate incorporated holmium (CaP-Ho) via sol-gel technique, and its characterization by XRD, FT-IR, NA and SEM. Results showed a multiphasic bioceramic composed mainly of hydroxyapatite, β-tricalcium phosphate, holmium phosphate and traces of calcium pyrophosphate. Furthermore, the nuclide Ho-166 was the major radioisotope produced. Despite that, the radioactive bioceramic CaP-166Ho must be investigated in clinical trials to assure its efficacy and safety on spine tumors treatment (author)

  8. Calcium phosphate holmium-166 ceramic to addition in bone cement: synthesis and characterization

    Energy Technology Data Exchange (ETDEWEB)

    Donanzam, Blanda A.; Campos, Tarcisio P.R., E-mail: campos@nuclear.ufmg.b [Universidade do Federal de Minas Gerais (DEN/UFMG), Belo Horizonte, MG (Brazil). Escola de Engenharia. Dept. de Engenharia Nuclear; Dalmazio, Ilza; Valente, Eduardo S., E-mail: id@cdtn.b, E-mail: valente@cdtn.b [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

    2011-07-01

    Spine metastases are a common and painful complication of cancer. The treatment often consists of bone cement injection (vertebroplasty or kyphoplasty) within vertebral body for vertebrae stabilization, followed by external beam radiation therapy. Recently, researchers introduced the concept of radioactive bone cement for spine tumors therapy. Then, investigations about bioactive and radioactive materials became interesting. In this study, we present the synthesis of calcium phosphate incorporated holmium (CaP-Ho) via sol-gel technique, and its characterization by XRD, FT-IR, NA and SEM. Results showed a multiphasic bioceramic composed mainly of hydroxyapatite, {beta}-tricalcium phosphate, holmium phosphate and traces of calcium pyrophosphate. Furthermore, the nuclide Ho-166 was the major radioisotope produced. Despite that, the radioactive bioceramic CaP-{sup 166}Ho must be investigated in clinical trials to assure its efficacy and safety on spine tumors treatment (author)

  9. Clinical and radiographic assessment of the efficacy of calcium silicate indirect pulp capping: a randomized controlled clinical trial.

    Science.gov (United States)

    Hashem, D; Mannocci, F; Patel, S; Manoharan, A; Brown, J E; Watson, T F; Banerjee, A

    2015-04-01

    The aims of this study were to assess the effectiveness of calcium silicate cement (Biodentine) versus glass ionomer cement (GIC; control group) as indirect pulp capping materials in patients with reversible pulpitis and to compare the effectiveness of cone beam computed tomography (CBCT) versus periapical (PA) radiographs in detecting PA changes at baseline (T0) and at 12 mo (T12) postoperatively. Seventy-two restorations (36 Biodentine, 36 Fuji IX) were placed randomly in 53 patients. CBCT/PA radiographs were taken at T0 and T12. Two calibrated examiners assessed the presence/absence and increase/decrease in the size of existing PA radiolucencies under standardized conditions. The Kappa coefficient evaluated statistically the effectiveness of CBCT versus PA radiographs in detecting PA changes. Chi-square/Mann-Whitney tests were used to evaluate the association between PA changes in CBCT with various clinical measures. Significance was predetermined at α = 0.05. Clinical success rates for Biodentine and Fuji IX GIC were 83.3%. CBCT was significantly more effective in detecting PA radiolucencies compared with radiographs (P = 0.0069). Of the teeth, 65.4% and 90.4% were deemed healthy using CBCT and PA radiographs, respectively, at T12. Healing/healed rates were 17.3%/0%, while new/progressed radiolucency were 30.8%/9.6% with CBCT/PA radiographs, respectively. Seventy-one percent of healed lesions had received Biodentine; 88% of new/progressed lesions received Fuji IX GIC. Teeth presenting with an initial CBCT PA lesion had a failure rate of 63%, whereas teeth with no initial lesion had a failure rate of 16%. Although no statistically significant difference was detected in the clinical efficacy of Biodentine/Fuji IX when used as indirect pulp capping materials in patients with reversible pulpitis, CBCT showed a significant difference in that most healed CBCT lesions had received Biodentine while most that did not heal received Fuji IX. Longer-term follow-up is

  10. Evaluation of pH, calcium ion release and antimicrobial activity of a new calcium aluminate cement

    Directory of Open Access Journals (Sweden)

    Fernanda de Carvalho Panzeri Pires-de-Souza

    2013-07-01

    Full Text Available This study evaluated the pH, calcium ion release and antimicrobial activity of EndoBinder (EB, containing different radiopacifiers: bismuth oxide (Bi2O3, zinc oxide (ZnO or zirconium oxide (ZrO2, in comparison to MTA. For pH and calcium ion release tests, 5 specimens per group (n = 5 were immersed into 10 mL of distilled and deionized water at 37°C. After 2, 4, 12, 24, 48 h; 7, 14 and 28 days, the pH was measured and calcium ion release quantified in an atomic absorption spectrophotometer. For antimicrobial activity, the cements were tested against S. aureus, E. coli, E. faecalis and C. albicans, in triplicate. MTA presented higher values for pH and calcium ion release than the other groups, however, with no statistically significant difference after 28 days (p > 0.05; and the largest inhibition halos for all strains, with no significant difference (E. coli and E. faecalis for pure EB and EB + Bi2O3 (p > 0.05. EB presented similar performance to that of MTA as regards pH and calcium ion release; however, when ZnO and ZrO2 were used, EB did not present antimicrobial activity against some strains.

  11. The In-situ Reinforcement of Calcium Phosphate Cement and Its Micro-structural Analysis

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    Carbon nanotubes ( CNTs ) and polyacrylic acid were employed to modify the setting process and hydration products of β- TCP/ TTCP calcium phosphate cement. The micro-structure of hydration product and the fashion of how additives and hydration particles interconnected were investigated. With the modification effect of CNTs, the setting particles and CNTs got winded and interconnected and thus made the composite more compact and denser.

  12. Indirect pulp therapy in a symptomatic mature molar using calcium enriched mixture cement

    OpenAIRE

    Hassan Torabzadeh; Saeed Asgary

    2013-01-01

    Dental pulp has the ability of repair/regeneration. Indirect pulp therapy (IPT) is recommended for pulp preservation in asymptomatic teeth with extremely deep caries as well as teeth with clinical symptoms of reversible pulpitis. In this case study, we performed IPT with calcium enriched mixture (CEM) cement on a symptomatic permanent molar. After clinical/radiographic examinations the tooth was diagnosed with irreversible pulpitis and associated apical periodontitis. IPT involved partial car...

  13. Preparation, Physical-Chemical Characterization, and Cytocompatibility of Polymeric Calcium Phosphate Cements

    Directory of Open Access Journals (Sweden)

    Rania M. Khashaba

    2011-01-01

    Full Text Available Aim. Physicochemical mechanical and in vitro biological properties of novel formulations of polymeric calcium phosphate cements (CPCs were investigated. Methods. Monocalcium phosphate, calcium oxide, and synthetic hydroxyapatite were combined with either modified polyacrylic acid, light activated polyalkenoic acid, or polymethyl vinyl ether maleic acid to obtain Types I, II, and III CPCs. Setting time, compressive and diametral strength of CPCs was compared with zinc polycarboxylate cement (control. Specimens were characterized using X-ray diffraction, scanning electron microscopy, and infrared spectroscopy. In vitro cytotoxicity of CPCs and control was assessed. Results. X-ray diffraction analysis showed hydroxyapatite, monetite, and brushite. Acid-base reaction was confirmed by the appearance of stretching peaks in IR spectra of set cements. SEM revealed rod-like crystals and platy crystals. Setting time of cements was 5–12 min. Type III showed significantly higher strength values compared to control. Type III yielded high biocompatibility. Conclusions. Type III CPCs show promise for dental applications.

  14. Fluorescent properties of a green- to red-emitting Eu3+, Tb3+ codoped amorphous calcium silicate phosphor

    International Nuclear Information System (INIS)

    A Eu3+, Tb3+ codoped amorphous calcium silicate phosphor was prepared by heating a Eu3+, Tb3+ codoped calcium silicate hydrate phosphor formed by liquid-phase reaction for 30 min at 900 °C. The excitation peak wavelength of the resulting phosphor was 379 nm and the emission peak wavelengths were at 542 nm, attributed to the 5D4→7F5 transition of Tb3+, and at 613 mm, attributed to the 5D0→7F1 transition of Eu3+. The intensity ratio of the two peaks could be freely controlled by varying the Eu/Tb atomic ratio of the Eu3+, Tb3+ codoped amorphous calcium silicate phosphor, allowing light to be emitted over a wide range from green to red. It was clarified that electron transfer from Tb3+ to Eu3+ is occurring. - Highlights: ► A Eu3+, Tb3+ codoped CSH phosphor was synthesized by liquid-phase reaction. ► CSH phosphor was heated at 900 °C to obtain Eu3+, Tb3+ codoped amorphous calcium silicate phosphor. ► Under 379 nm excitation, this phosphor showed emission peaks at 542 nm and 613 nm. ► The luminescent color could be continuously changed from green to red with increasing Eu/Tb atomic ratio. ► It was clarified that electron transfer from Tb3+ to Eu3+ is occurring.

  15. A chemical activity evaluation of two dental calcium silicate-based materials

    Directory of Open Access Journals (Sweden)

    Chalas Renata

    2015-06-01

    Full Text Available Calcium silicate-based materials are interesting products widely used in dentistry. The study was designed to compare the chemical reaction between analyzed two preparates and dentin during cavity lining. In our work, dentinal discs were prepared from human extracted teeth filled with Biodentine and MTA+. The samples were then analyzed by way of SEM, EDS and Raman spectroscopy. The obtained results revealed differences in elemental composition between both materials. Biodentine showed higher activity in contact with dentine. Moreover, the interfacial layer in the tooth filled by Biodentine was wider than that in the tooth filled with MTA+. The applied methods of analysis confirmed that both materials have a bioactive potential which is a promising ability.

  16. Influence of Hydrothermal Temperature on Phosphorus Recovery Efficiency of Porous Calcium Silicate Hydrate

    Directory of Open Access Journals (Sweden)

    Wei Guan

    2013-01-01

    Full Text Available Porous calcium silicate hydrate (PCSH was synthesized by carbide residue and white carbon black. The influence of hydrothermal temperature on phosphorus recovery efficiency was investigated by Field Emission Scanning Electron Microscopy (FESEM, Brunauer-Emmett-Teller (BET, and X-Ray Diffraction (XRD. Hydrothermal temperature exerted significant influence on phosphorus recovery performance of PCSH. Hydrothermal temperature 170°C for PCSH was more proper to recover phosphorus. PCSH could recover phosphorus with content of 18.51%. The law of Ca2+ and OH− release was the key of phosphorus recovery efficiency, and this law depended upon the microstructure of PCSH. When the temperature of synthesis reached to 170°C, the reactions between CaO and amorphous SiO2 were more efficient. Solubility of SiO2 was a limiting factor.

  17. Study of caesium adsorption on hydrated calcium-silicate-aluminate systems

    International Nuclear Information System (INIS)

    Immobilization of caesium in cementitious matrixes was studied in the present paper which is a key issue of handling radioactive caesium containig wastes for caesium does not form stabile compounds therefor it can not be readily immobilized. Model matrices were prepared to map up the calcium-silicate-aluminate system considering caesium immobilization, which were of different starting compositions. To caracterize Cs sorption, distribution ratios were determined. Based on the results obtained the model matrix compositions were prepared using industrial grade materials and their caesium retardation and trapping were examined by means of leaching and sorption experiments. In the light of the results obtained, it can be established that immobilization of caesium significantly depend on the starting composition of the used matrix. (orig.)

  18. Influence of Hydrothermal Temperature on Phosphorus Recovery Efficiency of Porous Calcium Silicate Hydrate

    International Nuclear Information System (INIS)

    Porous calcium silicate hydrate (PCSH) was synthesized by carbide residue and white carbon black. The influence of hydrothermal temperature on phosphorus recovery efficiency was investigated by Field Emission Scanning Electron Microscopy (FESEM), Brunauer-Emmett-Teller (BET), and X-Ray Diffraction (XRD). Hydrothermal temperature exerted significant influence on phosphorus recovery performance of PCSH. Hydrothermal temperature 170°C for PCSH was more proper to recover phosphorus. PCSH could recover phosphorus with content of 18.51%. The law of Ca2+ and OH− release was the key of phosphorus recovery efficiency, and this law depended upon the microstructure of PCSH. When the temperature of synthesis reached to 170°C, the reactions between CaO and amorphous SiO2 were more efficient. Solubility of SiO2 was a limiting factor.

  19. Optical properties and Judd–Ofelt analysis of Eu3+ activated calcium silicate

    International Nuclear Information System (INIS)

    Eu3+ activated calcium silicate was synthesized in stoichiometric ratio using the co-precipitation technique. The phosphors were characterized using X-ray diffraction and photoluminescence technique. Based on Judd–Ofelt (J–O) analysis, the intensity parameters Ω2 and Ω4 were calculated from the emission spectra for various Europium concentrations. The determined values indicate higher hypersensitive behavior of the 5D0→7F2 transition of Eu3+ ions in the host matrix and a stronger covalency. Different radiative properties have been discussed as the function of Eu3+ concentration. The lifetime decay pattern recorded for these samples indicated single exponential behavior. The quantum efficiency has been calculated to be 62% from the emission spectrum and the fluorescence lifetime was found to be 2.9 ms

  20. Thermal conductivity of the gadolinium calcium silicate apatites: Effect of different point defect types

    International Nuclear Information System (INIS)

    The apatite crystal structure of the gadolinium calcium silicates can accommodate a wide range of point defects, including oxygen and cation vacancies, as well as anti-site defects, depending on the Gd/Ca ratio. Compositions having only cation or oxygen vacancies were identified and the thermal diffusivity and conductivity were measured up to 1000 deg. C. All the compositions, including the stoichiometric composition, exhibit low thermal conductivities from room temperature to high temperature with the defect-containing compositions having even lower thermal conductivities. The high-temperature thermal conductivity, at temperatures below the onset of significant radiative heat transport, decreases with the inverse square root of the cation and anion vacancy concentration, consistent with simple defect scattering models. Based on the data, it is concluded that the oxygen vacancies are slightly more effective in reducing thermal conductivity.

  1. Luminescent, mesoporous, and bioactive europium-doped calcium silicate (MCS: Eu3+) as a drug carrier.

    Science.gov (United States)

    Fan, Yong; Huang, Shanshan; Jiang, Jinhua; Li, Guogang; Yang, Piaoping; Lian, Hongzhou; Cheng, Ziyong; Lin, Jun

    2011-05-15

    Luminescent, mesoporous, and bioactive europium-doped calcium silicate (MCS: Eu) was successfully synthesized. The obtained MCS: Eu(3+) was performed as a drug delivery carrier to investigate the drug storage/release properties using ibuprofen (IBU) as the model drug. The structural, morphological, textural, and optical properties were well characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), N(2) adsorption/desorption, and photoluminescence (PL) spectra, respectively. The results reveal that the MCS: Eu exhibits the typical ordered characteristics of the mesostructure. This composite shows a sustained release profile with IBU as the model drug. The IBU-loaded samples still present red luminescence of Eu(3+) ((5)D(0)-(7)F(1,2)) under UV irradiation. The emission intensities of Eu(3+) in the drug carrier system vary with the amount of released IBU, making the drug release easily tracked and monitored. The system demonstrates a great potential for drug delivery and disease therapy. PMID:21376337

  2. Optical properties and Judd–Ofelt analysis of Eu{sup 3+} activated calcium silicate

    Energy Technology Data Exchange (ETDEWEB)

    Barve, R.A., E-mail: rujuta_barve2003@yahoo.com; Suriyamurthy, N.; Panigrahi, B.S.; Venkatraman, B.

    2015-10-15

    Eu{sup 3+} activated calcium silicate was synthesized in stoichiometric ratio using the co-precipitation technique. The phosphors were characterized using X-ray diffraction and photoluminescence technique. Based on Judd–Ofelt (J–O) analysis, the intensity parameters Ω{sub 2} and Ω{sub 4} were calculated from the emission spectra for various Europium concentrations. The determined values indicate higher hypersensitive behavior of the {sup 5}D{sub 0}→{sup 7}F{sub 2} transition of Eu{sup 3+} ions in the host matrix and a stronger covalency. Different radiative properties have been discussed as the function of Eu{sup 3+} concentration. The lifetime decay pattern recorded for these samples indicated single exponential behavior. The quantum efficiency has been calculated to be 62% from the emission spectrum and the fluorescence lifetime was found to be 2.9 ms.

  3. Evaluation of shear bond strength of two resin-based composites and glass ionomer cement to pure tricalcium silicate-based cement (Biodentine®

    Directory of Open Access Journals (Sweden)

    Kenan CANTEK?N

    2014-07-01

    Full Text Available Objectives: Tricalcium silicate is the major constituent phase in mineral trioxide aggregate (MTA. It is thus postulated that pure tricalcium silicate can replace the Portland cement component of MTA. The aim of this study was to evaluate bond strength of methacrylate-based (MB composites, silorane-based (SB composites, and glass ionomer cement (GIC to Biodentine® and mineral trioxide aggregate (MTA. Material and Methods: Acrylic blocks (n=90, 2 mm high, 5 mm diameter central hole were prepared. In 45 of the samples, the holes were fully filled with Biodentine® and in the other 45 samples, the holes were fully filled with MTA. The Biodentine® and the MTA samples were randomly divided into 3 subgroups of 15 specimens each: Group-1: MB composite; Group-2: SB composite; and Group-3: GIC. For the shear bond strength (SBS test, each block was secured in a universal testing machine. Results: The highest (17.7±6.2 MPa and the lowest (5.8±3.2 MPa bond strength values were recorded for the MB composite-Biodentine® and the GIC-MTA, respectively. Although the MB composite showed significantly higher bond strength to Biodentine (17.7±6.2 than it did to MTA (8.9±5.7 (p<0.001, the SB composite (SB and MTA=7.4±3.3; SB and Biodentine®=8.0±3,6 and GIC (GIC and MTA=5.8±3.2; GIC and Biodentine=6.7±2.6 showed similar bond strength performance with MTA compared with Biodentine (p=0.73 and p=0.38, respectively. Conclusions: The new pure tricalcium-based pulp capping, repair, and endodontic material showed higher shear bond scores compared to MTA when used with the MB composite.

  4. In situ hydroxyapatite nanofiber growth on calcium borate silicate ceramics in SBF and its structural characteristics

    Energy Technology Data Exchange (ETDEWEB)

    Pu, Yinfu; Huang, Yanlin; Qi, Shuyun [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Chen, Cuili [Department of Physics and Interdisciplinary Program of Biomedical, Mechanical & Electrical Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of); Seo, Hyo Jin, E-mail: hjseo@pknu.ac.kr [Department of Physics and Interdisciplinary Program of Biomedical, Mechanical & Electrical Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of)

    2015-10-01

    A novel calcium silicate borate Ca{sub 11}Si{sub 4}B{sub 2}O{sub 22} ceramic was firstly prepared by the conventional solid-state reaction. In vitro hydroxyapatite mineralization was investigated by soaking the ceramics in simulated body fluid (SBF) solutions at body temperature (37 °C) for various time periods. Scanning electron microscopy (SEM) and X-ray diffraction analysis (XRD) measurements were applied to investigate the samples before and after the immersion of ceramics in SBF solution. The elemental compositions of a hydroxyapatite layer on the ceramics during the mineralization were confirmed by X-ray energy-dispersive spectra (EDS). Meanwhile, the bending strength and elastic modulus of Ca{sub 11}Si{sub 4}B{sub 2}O{sub 22} ceramics were also measured, which indicate that the biomaterials based on Ca{sub 11}Si{sub 4}B{sub 2}O{sub 22} ceramics possess bioactivity and might be a potential candidate as biomaterials for hard tissue repair. The bioactive mineralization ability was evaluated on the base of its crystal structural characteristics, i.e., silanol (Si–OH) and B–OH groups can be easily induced on the surface of Ca{sub 11}Si{sub 4}B{sub 2}O{sub 22} ceramics soaked in SBF solutions. - Highlights: • Calcium silicate borate Ca{sub 11}Si{sub 4}B{sub 2}O{sub 22} ceramics were developed as a new biomaterial. • Ca{sub 11}Si{sub 4}B{sub 2}O{sub 22} shows a superior in vitro bioactivity by inducing bone-like apatite. • Ca{sub 11}Si{sub 4}B{sub 2}O{sub 22} has good mechanical properties as potential candidate biomaterials. • The structure with SiO{sub 4} and BO{sub 3} groups is favorable for hydroxyapatite formation.

  5. Fractionation and solubility of cadmium in paddy soils amended with porous hydrated calcium silicate

    Institute of Scientific and Technical Information of China (English)

    ZHAO Xiu-lan; Saigusa Masaihiko

    2007-01-01

    Previous studies have shown that porous hydrated calcium silicate(PS)is very effective in decreasing cadmium(Cd)content in brown rice.However,it is unclear whether me PS influences cadmium transformation in soil.The present study examined the effect of PS on pH,cadmium transformation and cadmium solubility in Andosol and Alluvial soil,and also compared its effects with CaCO3,acidic porous hydrated calcium silicate(APS)and silica gel.Soil cadmium was operationally fractionationed into exchangeable(Exch),bound to carbonates(Carb).bound to iron and manganese oxides(FeMnOx),bound to organic matters(OM)and residual(Res)fraction.ApplicatiOn of PS and CaCO3 at hig rates enhanced soil pH,while APS and silica gel did not obviously change soil pH.PS and CaCO3 also increased the FeMnOx-Cd in Andosol and Carb-Cd in Alluvial soil,thus reducing the Exch-Cd in me tested soils.However,PS was less effecfive than CaCO3 at the same application rate.Cadmium fractions in the two soils were not changed by the treatments of APS and silica gel.There were no obvious differences in the solubility of cadmium in soils treated with PS,APS,silica gel and CaCO3 except Andosol treated 2.0%CaCO3 at the same pH of soil-CaCl2 suspensions.These findings suggested that the decrease of cadmium availability in soil was mainly attributed to the increase of soil pH caused by PS.

  6. In situ hydroxyapatite nanofiber growth on calcium borate silicate ceramics in SBF and its structural characteristics

    International Nuclear Information System (INIS)

    A novel calcium silicate borate Ca11Si4B2O22 ceramic was firstly prepared by the conventional solid-state reaction. In vitro hydroxyapatite mineralization was investigated by soaking the ceramics in simulated body fluid (SBF) solutions at body temperature (37 °C) for various time periods. Scanning electron microscopy (SEM) and X-ray diffraction analysis (XRD) measurements were applied to investigate the samples before and after the immersion of ceramics in SBF solution. The elemental compositions of a hydroxyapatite layer on the ceramics during the mineralization were confirmed by X-ray energy-dispersive spectra (EDS). Meanwhile, the bending strength and elastic modulus of Ca11Si4B2O22 ceramics were also measured, which indicate that the biomaterials based on Ca11Si4B2O22 ceramics possess bioactivity and might be a potential candidate as biomaterials for hard tissue repair. The bioactive mineralization ability was evaluated on the base of its crystal structural characteristics, i.e., silanol (Si–OH) and B–OH groups can be easily induced on the surface of Ca11Si4B2O22 ceramics soaked in SBF solutions. - Highlights: • Calcium silicate borate Ca11Si4B2O22 ceramics were developed as a new biomaterial. • Ca11Si4B2O22 shows a superior in vitro bioactivity by inducing bone-like apatite. • Ca11Si4B2O22 has good mechanical properties as potential candidate biomaterials. • The structure with SiO4 and BO3 groups is favorable for hydroxyapatite formation

  7. A New Type of Biphasic Calcium Phosphate Cement as a Gentamicin Carrier for Osteomyelitis

    Directory of Open Access Journals (Sweden)

    Wen-Yu Su

    2013-01-01

    Full Text Available Osteomyelitis therapy is a long-term and inconvenient procedure for a patient. Antibiotic-loaded bone cements are both a complementary and alternative treatment option to intravenous antibiotic therapy for the treatment of osteomyelitis. In the current study, the biphasic calcium phosphate cement (CPC, called α-TCP/HAP (α-tricalcium phosphate/hydroxyapatite biphasic cement, was prepared as an antibiotics carrier for osteomyelitis. The developed biphasic cement with a microstructure of α-TCP surrounding the HAP has a fast setting time which will fulfill the clinical demand. The X-ray diffraction and Fourier transform infrared spectrometry analyses showed the final phase to be HAP, the basic bone mineral, after setting for a period of time. Scanning electron microscopy revealed a porous structure with particle sizes of a few micrometers. The addition of gentamicin in α-TCP/HAP would delay the transition of α-TCP but would not change the final-phase HAP. The gentamicin-loaded α-TCP/HAP supplies high doses of the antibiotic during the initial 24 hours when they are soaked in phosphate buffer solution (PBS. Thereafter, a slower drug release is produced, supplying minimum inhibitory concentration until the end of the experiment (30 days. Studies of growth inhibition of Staphylococcus aureus and Pseudomonas aeruginosa in culture indicated that gentamicin released after 30 days from α-TCP/HAP biphasic cement retained antibacterial activity.

  8. Influence of the use of nanoscale siliceous cement system on the strength

    Directory of Open Access Journals (Sweden)

    KOSACH Anatoliy Fyodorovich

    2014-06-01

    Full Text Available The article is devoted to creation of scientific basis for cement stone structure formation, development of optimal compositions and technology for manufacturing building materials based on the waste of fine-grained pure quartz production. This technology provides significant pore filling, formation of new crystallization centers which act as an dditional reinforcement of cement hydration products, and increase of physical and mechanical properties.

  9. Effect of calcium sulfates on the early hydration of calcium sulfoaluminate cement and the stability of embedded aluminium

    International Nuclear Information System (INIS)

    Conventional Portland cement-based systems have been considered unsuitable for immobilising nuclear wastes containing reactive metals, such as aluminium, due to the high pH of the pore solution (usually around 12.5) and free moisture. On the contrary, calcium sulfo-aluminate cement (CSA) produces a lower pH (10.5-12) environment and has an excellent water binding capability as a result of the formation of its main hydration product, ettringite. Therefore, it offers a good potential to immobilise aluminium. However, the pore solution pH and ettringite formation depend largely on the raw materials used to formulate the CSA, which is usually a blend of 75%-85% of CSA clinker and 15-25% of calcium sulfate (in the form of gypsum or anhydrite). In this paper, it was found that, compared to anhydrite, gypsum (15% wt of the blend) demonstrated the highest reduction in the corrosion of embedded Al, possibly due to its lower initial pH (around 10.5) and self-desiccating nature at the early stage of hydration. Whilst the CSA/anhydrite had a higher Al corrosion rate, the initial set was more acceptable than CSA/gypsum. Nonetheless, overall, it was concluded that CSA with gypsum (15% wt) should be considered as a base formulation for the encapsulation of Al waste. The unfavorable rapid set and high heat generation, however, demonstrated that modifications are required, potentially by using mineral additions. (authors)

  10. Calcium looping spent sorbent as a limestone replacement in the manufacture of portland and calcium sulfoaluminate cements.

    Science.gov (United States)

    Telesca, Antonio; Marroccoli, Milena; Tomasulo, Michele; Valenti, Gian Lorenzo; Dieter, Heiko; Montagnaro, Fabio

    2015-06-01

    The calcium looping (CaL) spent sorbent (i) can be a suitable limestone replacement in the production of both ordinary Portland cement (OPC) and calcium sulfoaluminate (CSA) cement, and (ii) promotes environmental benefits in terms of reduced CO2 emission, increased energy saving and larger utilization of industrial byproducts. A sample of CaL spent sorbent, purged from a 200 kWth pilot facility, was tested as a raw material for the synthesis of two series of OPC and CSA clinkers, obtained from mixes heated in a laboratory electric oven within temperature ranges 1350°-1500 °C and 1200°-1350 °C, respectively. As OPC clinker-generating mixtures, six clay-containing binary blends were investigated, three with limestone (reference mixes) and three with the CaL spent sorbent. All of them showed similar burnability indexes. Moreover, three CSA clinker-generating blends (termed RM, MA and MB) were explored. They included, in the order: (I) limestone, bauxite and gypsum (reference mix); (II) CaL spent sorbent, bauxite and gypsum; (III) CaL spent sorbent plus anodization mud and a mixture of fluidized bed combustion (FBC) fly and bottom ashes. The maximum conversion toward 4CaO·3Al2O3·SO3, the chief CSA clinker component, was the largest for MB and almost the same for RM and MA. PMID:25915150

  11. The Retentive Strength of Cemented Zirconium Oxide Crowns after Dentin Pretreatment with Desensitizing Paste Containing 8% Arginine and Calcium Carbonate.

    Science.gov (United States)

    Pilo, Raphael; Harel, Noga; Nissan, Joseph; Levartovsky, Shifra

    2016-01-01

    The effect of dentin pretreatment with Desensitizing Paste containing 8% arginine and calcium carbonate on the retention of zirconium oxide (Y-TZP) crowns was tested. Forty molar teeth were mounted and prepared using a standardized protocol. Y-TZP crowns were produced using computer-aided design and computer-aided manufacturing (CAD-CAM) technology. The 40 prepared teeth were either pretreated with Desensitizing Paste or not pretreated. After two weeks, each group was subdivided into two groups, cemented with either Resin Modified Glass Ionomer Cement (RMGIC) or Self Adhesive Resin Cement (SARC)). Prior to cementation, the surface areas of the prepared teeth were measured. After aging, the cemented crown-tooth assemblies were tested for retentive strength using a universal testing machine. The debonded surfaces of the teeth and crowns were examined microscopically at 10× magnification. Pretreating the dentin surfaces with Desensitizing Paste prior to cementation did not affect the retention of the Y-TZP crowns. The retentive values for RMGIC (3.04 ± 0.77 MPa) were significantly higher than those for SARC (2.28 ± 0.58 MPa). The predominant failure modes for the RMGIC and SARC were adhesive cement-dentin and adhesive cement-crown, respectively. An 8.0% arginine and calcium carbonate in-office desensitizing paste can be safely used to reduce post-cementation sensitivity without reducing the retentive strength of Y-TZP crowns. PMID:27023532

  12. The Retentive Strength of Cemented Zirconium Oxide Crowns after Dentin Pretreatment with Desensitizing Paste Containing 8% Arginine and Calcium Carbonate

    Directory of Open Access Journals (Sweden)

    Raphael Pilo

    2016-03-01

    Full Text Available The effect of dentin pretreatment with Desensitizing Paste containing 8% arginine and calcium carbonate on the retention of zirconium oxide (Y-TZP crowns was tested. Forty molar teeth were mounted and prepared using a standardized protocol. Y-TZP crowns were produced using computer-aided design and computer-aided manufacturing (CAD-CAM technology. The 40 prepared teeth were either pretreated with Desensitizing Paste or not pretreated. After two weeks, each group was subdivided into two groups, cemented with either Resin Modified Glass Ionomer Cement (RMGIC or Self Adhesive Resin Cement (SARC. Prior to cementation, the surface areas of the prepared teeth were measured. After aging, the cemented crown-tooth assemblies were tested for retentive strength using a universal testing machine. The debonded surfaces of the teeth and crowns were examined microscopically at 10× magnification. Pretreating the dentin surfaces with Desensitizing Paste prior to cementation did not affect the retention of the Y-TZP crowns. The retentive values for RMGIC (3.04 ± 0.77 MPa were significantly higher than those for SARC (2.28 ± 0.58 MPa. The predominant failure modes for the RMGIC and SARC were adhesive cement-dentin and adhesive cement-crown, respectively. An 8.0% arginine and calcium carbonate in-office desensitizing paste can be safely used to reduce post-cementation sensitivity without reducing the retentive strength of Y-TZP crowns.

  13. Interaction of Nanostructured Calcium Silicate Hydrate with Ibuprofen Drug Molecules: X-ray Absorption Near Edge Structure (XANES) Study at the Ca, Si and O K-edge

    International Nuclear Information System (INIS)

    Mesoporous calcium silicate hydrate (CSH) nanostructure has been proven to be bioactive and biocompatible, and has a bright future in the application of bone treatment among other applications. X-ray absorption near edge structure (XANES) is a powerful tool for the study of the interactions of calcium silicate hydrates with drug molecules because it is element specific and it probes the unoccupied electronic states. Herein, we report the use of the calcium, silicon and oxygen K-edge XANES spectroscopy to identify how drug molecules interact with different groups in calcium silicate hydrate mesoporous nano-carriers with different morphologies. Significant changes are observed in XANES spectra after drug loading into the calcium silicate hydrate system, especially at the Si and O K-edge. The implications of these findings are discussed.

  14. Augmentation of femoral neck fracture fixation with an injectable calcium-phosphate bone mineral cement.

    Science.gov (United States)

    Stankewich, C J; Swiontkowski, M F; Tencer, A F; Yetkinler, D N; Poser, R D

    1996-09-01

    The first goal of this study was to determine if augmentation with an injectable, in situ setting, calcium-phosphate cement that is capable of being remodeled and was designed to mimic bone mineral significantly improved the strength and stiffness of fixation in a cadaveric femoral neck fracture model. The second goal was to determine if greater increases in fixation strength were achieved as the bone density of the specimen decreased. Sixteen pairs of fresh cadaveric human femora with a mean age of 70.9 years (SD = 17.2 years) were utilized. The bone density of the femoral neck was measured with dual-energy x-ray absorptiometry. The femoral head was impacted vertically with the femoral shaft fixed in 12 degrees of adduction using a materials testing machine to create a fully displaced fracture. Following fracture, 30% inferior comminution was created in each specimen. One randomly chosen femur from each pair underwent anatomic reduction and fixation with three cannulated cancellous bone screws, 7 mm in diameter, in an inverted triangle configuration. The contralateral femur underwent the same fixation augmented with calcium-phosphate cement. Specimens were preconditioned followed by 1.000 cycles to one body weight (611.6 N) at 0.5 Hz to simulate single-limb stance loading. The stiffness in the first cycle was observed to be significantly greater in cement-augmented specimens compared with unaugmented controls (p bone mineral cement failed at a mean of 4,573 N (SD = 1,243 N); this was significantly greater (p bone density (p = 0.25, R2 = 0.09), was weakly correlated to the volume of cement injected (p = 0.07, R2 = 0.22), and was inversely related to the fixation failure load of the control specimen (p = 0.001, R2 = 0.54). There was a mean relative improvement in fixation strength of 169.6% (SD = 77.5). These findings suggest that calcium-phosphate cement provides initial beneficial augmentation to fixation of femoral neck fractures. PMID:8893773

  15. Calcium-enriched mixture cement as artificial apical barrier: A case series

    Directory of Open Access Journals (Sweden)

    Ali Nosrat

    2011-01-01

    Full Text Available In comparison to the conventional apexification using calcium hydroxide, artificial apical barrier technique is more valuable and less time consuming. This article describes successful use of calcium-enriched mixture (CEM cement as an artificial apical barrier in open apices. In this study, 13 single-rooted teeth with necrotic pulps and open apices were treated non-surgically. After copious irrigation of the root canals with NaOCl 5.25% and gentle filing, based on need for interappointment dressing, treatments were followed by CEM cement (BioniqueDent, Tehran, Iran apical plug insertion in the first or second appointment. All cases were then permanently restored. All subjects were followed until radiographic evidence of periradicular healing was seen (mean 14.5 months. Clinically, all cases were functional and asymptomatic and complete osseous healing was observed in all the teeth. Considering the biological properties of CEM cement, this new endodontic biomaterial might be appropriate to be used as artificial apical barrier in the open apex teeth.

  16. Synthesis and nano-mechanical characterization of calcium-silicate-hydrate (C-S-H) made with 1.5 CaO/SiO2 mixture

    International Nuclear Information System (INIS)

    In this study, calcium silicate hydrate (C-S-H) is synthesized and characterized. C-S-H slurry was made with calcium oxide (CaO) to micro-silica (SiO2) mixture ratio of 1.5 and enough deionized water. The slurry was continuously mixed for 7 days, then the excess water was removed. Two methods of drying were implemented: one method used the standard d-dry technique and the other was equilibrated to 11% relative humidity (RH). The dried powders were characterized using thermo gravimetric analysis (TGA), X-ray diffraction analysis (XRDA), and 29Si magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy. The stoichiometric formulas of synthetic C-S-H powders dried to d-dry and 11% RH in this study were approximated as C1.2SH0.7 and C1.2SH2.4 respectively. The powders were then compacted to create specimens with porosities similar to C-S-H in hydrated cement. The specimens underwent nanoindentation to mechanically characterize C-S-H. The experiments provide insight on the nanoscale mechanical characteristics of C-S-H.

  17. Fluorescence Properties and Synthesis of Green-Emitting Tb3+-Activated Amorphous Calcium Silicate Phosphor by Ultraviolet Irradiation of 378 nm

    OpenAIRE

    Yoshiyuki Kojima; Masaaki Numazawa; Shinnosuke Kamei; Nobuyuki Nishimiya

    2012-01-01

    The excitation wavelength of conventional Tb3+-activated phosphor is near 270 nm. This study describes novel green-emitting Tb3+-activated amorphous calcium silicate by ultraviolet excitation at 378 nm. The Tb3+-activated amorphous calcium silicate was prepared by heating a sample of Tb3+-activated calcium silicate hydrate (CSH) at 900°C for 30 minutes. The emission wavelength of the resulting phosphor was 544 nm. The optimum excitation wavelength within the range 300–400 nm was 378 nm. The T...

  18. Influence of saline solution on hydration behavior of β-dicalcium silicate in comparison with biphasic calcium phosphate/hydroxyapatite bio-ceramics

    International Nuclear Information System (INIS)

    The influence of using saline solution as mixing and curing liquid on some characteristics of β-dicalcium silicate (β-C2S) and biphasic compound tri-calcium phosphate/hydroxyapatite (TCP/HAp) bio-ceramics was investigated. β-C2S (27–30 nm) was prepared by solid state reaction at 1450 °C, while biphasic compound TCP/HAp (7–15 nm) was synthesized from an aqueous solution of Ca(NO3)2·4H2O and (NH4)2HPO4·12H2O by chemical precipitation method. Setting times, compressive strength, pH values, X-ray diffraction analysis, infrared spectroscopy, scanning electron microscopy (SEM) were investigated. The evaluation of cytotoxicity of both calcium silicate and biphasic compounds to human gingival fibroblasts was carried out. The use of saline solution as mixing and immersing liquid shortened the setting time for the two bio-cements. TCP/HAp did not show any mechanical strength but β-C2S showed good strength values. Both synthesized compounds showed a moderate cytotoxicity and both materials were effective in a no significant way. - Highlights: • The dissolution and hydration of β-C2S and TCP/HAp in distilled water and saline solution were studied. • TCP/HAp did not show mechanical strength, while β-C2S showed good mechanical strength. • The use of saline solution did enhances the dissolution & hydration rate. • An increase in pH values was detected when using saline solution. • Both materials showed a moderate cytotoxicity in no significant way

  19. Influence of saline solution on hydration behavior of β-dicalcium silicate in comparison with biphasic calcium phosphate/hydroxyapatite bio-ceramics

    Energy Technology Data Exchange (ETDEWEB)

    Radwan, M.M., E-mail: mmahmoudradwan@yahoo.com [Ceramics Dept, National Research Centre, Cairo (Egypt); Abd El-Hamid, H.K. [Ceramics Dept, National Research Centre, Cairo (Egypt); Mohamed, A.F. [The Holding Company for Production of Vaccines, Sera and Drugs (EGYVAC) (Egypt)

    2015-12-01

    The influence of using saline solution as mixing and curing liquid on some characteristics of β-dicalcium silicate (β-C{sub 2}S) and biphasic compound tri-calcium phosphate/hydroxyapatite (TCP/HAp) bio-ceramics was investigated. β-C{sub 2}S (27–30 nm) was prepared by solid state reaction at 1450 °C, while biphasic compound TCP/HAp (7–15 nm) was synthesized from an aqueous solution of Ca(NO{sub 3}){sub 2}·4H{sub 2}O and (NH{sub 4}){sub 2}HPO{sub 4}·12H{sub 2}O by chemical precipitation method. Setting times, compressive strength, pH values, X-ray diffraction analysis, infrared spectroscopy, scanning electron microscopy (SEM) were investigated. The evaluation of cytotoxicity of both calcium silicate and biphasic compounds to human gingival fibroblasts was carried out. The use of saline solution as mixing and immersing liquid shortened the setting time for the two bio-cements. TCP/HAp did not show any mechanical strength but β-C{sub 2}S showed good strength values. Both synthesized compounds showed a moderate cytotoxicity and both materials were effective in a no significant way. - Highlights: • The dissolution and hydration of β-C{sub 2}S and TCP/HAp in distilled water and saline solution were studied. • TCP/HAp did not show mechanical strength, while β-C{sub 2}S showed good mechanical strength. • The use of saline solution did enhances the dissolution & hydration rate. • An increase in pH values was detected when using saline solution. • Both materials showed a moderate cytotoxicity in no significant way.

  20. Investigation of fresh and hardened properties of Calcium sulfoaluminate (CSA cement blends

    Directory of Open Access Journals (Sweden)

    P. Herrmann

    2014-05-01

    Full Text Available Calcium sulfoaluminate (CSA is a comparatively new cementitious material that is mainly established in China where it is produced in a large scale. CSA cement is not covered by European standards. However, it provides different beneficial properties such as rapid hardening and high early strength development. Furthermore, the usage of CSA cement can save energy during production process in comparison to established cementitious materials. Therefore it is also more environmental friendly. Insufficient knowledge of this material behaviour restricts the possibilities and makes further research necessary. The research project applied a laboratory test program to elaborate the characterization of the materials. The obtained knowledge from these tests was then applied to further tests to determine application relevant key properties of CSA based pastes and mortars.The properties of pure CSA cement had been compared with the properties of CSA blends. The additions were PC, HAC, FA and GGBS with quantities of 10, 20 and 30%. The water to cement ratio was varying between 0.4, 0.5 and 0.6. General tests like fineness, XRD and XRF were used to define the present non-standardized material. Investigation of fresh pastes included measurement of setting time and calorimetry. Hardened mortar specimens of different ages were examined for compressive strength. The results showed that CSA itself hardens very rapidly and gives an early strength development. Possible ways of utilization of CSA based mortars and concretes were also emphasized in the paper.

  1. The effect of supplementary pulverized fuel ash on calcium aluminate phosphate cement for intermediate-level waste encapsulation

    International Nuclear Information System (INIS)

    The objective of the current study was to evaluate the effects of supplementary pulverized fuel ash on phosphate-modified calcium aluminate cement. These systems are being established as part of a wider project to develop alternative cementing systems for the encapsulation of problematic low- and intermediate- level radioactive waste in the UK. The nuclear industry has established specific processing and property criteria, which must be fulfilled to ensure suitability for industrial application. In a series of studies, pulverized fuel ash was used as a partial replacement for calcium aluminate cement, to improve the fluidity of the system and increase the setting time. Properties such as slurry pH and fluidity, setting time, mechanical properties, and porosity were investigated using Vicat, Colflow, and compressive strength testing equipment and mercury intrusion porosimetry. The hardened cement pastes were also characterised using X-ray diffraction, thermogravimetric analysis and scanning electron microscopy. A formulation envelope was identified, which fulfilled the plant acceptance tests defined by industry to ensure suitability for industrial application. It was found that pH of calcium aluminate phosphate cements is lower than that of conventional cementing systems used to encapsulate radioactive waste in the UK. Hence, they have potential to be used as an alternative cementing system for the encapsulation of problematic radioactive metals. (authors)

  2. Modifications on the properties of a calcium phosphate cement by additions of sodium alginate

    Energy Technology Data Exchange (ETDEWEB)

    Coelho, W.T.; Fernandes, J.M.; Vieira, R.S.; Thurmer, M.B.; Santos, L.A., E-mail: trajano@ufrgs.br, E-mail: julianafernandes2@yahoo.com.br, E-mail: rsvieira.eng@gmail.com, E-mail: monicathurmer@yahoo.com.br, E-mail: luis.santos@ufrgs.br [Universidade Federal do Rio Grande do Sul (PPG/LABIOMAT/UFRGS), RS (Brazil)

    2012-07-01

    The Calcium Phosphate Cement (CPC) are bone substitutes with great potential for use in orthopedics, traumatology and dentistry due to its biocompatibility, bioactivity and osteoconductivity, and form a paste that can be easily shaped and placed into the surgical site. However, CPCs have low mechanical strength, which equals the maximum mechanical strength of trabecular bone. In order to assess the strength and time to handle a CPC composed primarily of alpha phase, were added sodium alginate (1%, 2% and 3% wt) and an accelerator in an aqueous solution. The cement powder was mixed with liquid of setting, shaped into specimens and evaluated for apparent density and porosity by Archimedes method, X-ray diffraction and compressive strength. A significant increase in compressive strength by adding sodium alginate was verified. (author)

  3. Modifications on the properties of a calcium phosphate cement by additions of sodium alginate

    International Nuclear Information System (INIS)

    The Calcium Phosphate Cement (CPC) are bone substitutes with great potential for use in orthopedics, traumatology and dentistry due to its biocompatibility, bioactivity and osteoconductivity, and form a paste that can be easily shaped and placed into the surgical site. However, CPCs have low mechanical strength, which equals the maximum mechanical strength of trabecular bone. In order to assess the strength and time to handle a CPC composed primarily of alpha phase, were added sodium alginate (1%, 2% and 3% wt) and an accelerator in an aqueous solution. The cement powder was mixed with liquid of setting, shaped into specimens and evaluated for apparent density and porosity by Archimedes method, X-ray diffraction and compressive strength. A significant increase in compressive strength by adding sodium alginate was verified. (author)

  4. Graphene-reinforced calcium silicate coatings for load-bearing implants

    International Nuclear Information System (INIS)

    Owing to the superior mechanical properties and low coefficient of thermal expansion, graphene has been widely used in the reinforcement of ceramics. In the present study, various ratios of graphene (0.5 wt%, 1.5 wt% and 4 wt%) were reinforced into calcium silicate (CS) coatings for load-bearing implant surface modification. Surface characteristics of the graphene/calcium silicate (GC) composite coatings were characterized by scanning electron microscopy. Results show that the graphene plates (less than 4 wt% in the coatings) were embedded in the CS matrix homogeneously. The surfaces of the coatings showed a hierarchical hybrid nano-/microstructure, which is believed to be beneficial to the behaviors of the cell and early bone fixation of the implants. Wear resistance measured by a pin-on-disc model exhibited an obvious enhancement with the adoption of graphene plates. The weight losses of the GC coatings decreased with the increase of graphene content. However, too high graphene content (4 wt% or more) made the composite coatings porous and the wear resistance decreased dramatically. The weight loss was only 1.3 ± 0.2 mg for the GC coating containing 1.5 wt% graphene (denoted as GC1.5) with a load of 10 N and sliding distance of 500 m, while that of the pure CS coating reached up to 28.6 ± 0.5 mg. In vitro cytocompatibility of the GC1.5 coating was evaluated using a human marrow stem cell (hMSC) culture system. The proliferation and alkaline phosphatase, osteopontin and osteocalcin (OC) osteogenesis-related gene expression of the cells on the GC1.5 coating did not deteriorate with the adoption of graphene. Conversely, even better adhesion of the hMSCs was observed on the GC1.5 coating than on the pure CS coating. All of the results indicate that the GC1.5 coating is a good candidate for load-bearing implants. (paper)

  5. Characterization of a calcium phosphate cement based on alpha-tricalcium phosphate obtained by wet precipitation process

    International Nuclear Information System (INIS)

    There are several systems of calcium phosphate cements being studied. Those based on alpha-tricalcium phosphate are of particular interest. After setting they produce calcium deficient hydroxyapatite similar to bone like hydroxyapatite. This work aims to obtain alpha-tricalcium phosphate powders by the wet precipitation process, using calcium nitrate and phosphoric acid as reagents. This powder was characterized by infrared spectroscopy, X-ray diffraction and particle size distribution. In order to prepare the calcium phosphate cement, the powder was mixed with an accelerator in an aqueous solution. The mechanical properties of the cement were assessed and it was evaluated by means of apparent density, X-ray diffraction and scanning electron microscopy. The described method produced crystalline alpha-tricalcium phosphate as the major phase. The calcium phosphate cement showed high values of compression strength (50 MPa). The soaking of the cement in a simulated body fluid (SBF) formed a layer of hydroxyapatite like crystals in the surface of the samples. (author)

  6. The progress of early phase bone healing using porous granules produced from calcium phosphate cement

    Directory of Open Access Journals (Sweden)

    Jungbluth P

    2010-05-01

    Full Text Available Abstract Objective Bone grafting is a vital component in many surgical procedures to facilitate the repair of bone defects or fusions. Autologous bone has been the gold standard to date in spite of associated donor-site morbidity and the limited amount of available donor bone. The aim of this study was to investigate the progress of bone regeneration and material degradation of calcium phosphate granules (CPG produced from a calcium phosphate self-setting cement powder compared to the use of autologous bone grafting in the treatment of "critical size defects" on load-bearing long bones of minipigs. Methods A critical size defect in the tibial metaphysis of 16 mini-pigs was filled either with autologous cancellous graft or with micro- and macroporous carbonated, apatic calcium phosphate granules (CPG produced from a calcium phosphate self-setting cement powder. After 6 weeks, the specimens were assessed by X-ray and histological evaluation. The amount of new bone formation was analysed histomorphometrically. Results The semi-quantitative analysis of the radiological results showed a complete osseous bridging of the defect in three cases for the autograft group. In the same group five animals showed a beginning, but still incomplete bridging of the defect, whereas in the CPG group just two animals developed this. All other animals of the CPG group showed only a still discontinuous new bone formation. Altogether, radiologically a better osseous bridging was observed in the autograft group compared to the CPG group. Histomorphometrical analysis after six weeks of healing revealed that the area of new bone was significantly greater in the autograft group concerning the central area of the defect zone (p Conclusions Within the limits of the present study it could be demonstrated that autologous cancellous grafts lead to a significantly better bone regeneration compared to the application of calcium phosphate granules (CPG produced from a calcium

  7. The compressive modulus and strength of saturated calcium sulphate dihydrate cements: implications for testing standards.

    Science.gov (United States)

    Koh, Ilsoo; López, Alejandro; Helgason, Benedikt; Ferguson, Stephen J

    2014-06-01

    Calcium sulphate-based bone cement is a bone filler with proven biological advantages including biodegradability, biocompatibility and osteoconductivity. Mechanical properties of such brittle ceramic cements are frequently determined using the testing standard designed for ductile acrylic cements. The aims of the study were (1) to validate the suitability of this common testing protocol using saturated calcium sulphate dihydrate (CSD), and (2) to compare the strength and effective modulus of non-saturated and saturated CSD, in order to determine the changes in the mechanical behavior of CSD upon saturation. Unconfined compression tests to failure were performed on 190 cylindrical CSD samples. The samples were divided into four groups having different saturation levels (saturated, non-saturated) and end conditions (capped and non-capped). Two effective moduli were calculated per sample, based on the deformations measured using the machine platens and a sample-mounted extensometer. The effective moduli of non-saturated groups were found to be independent of the end conditions. The saturated and capped group showed no difference in the effective moduli derived from different measurement methods, while the saturated and non-capped group showed a significant difference between the machine platen- and extensometer-derived moduli. Strength and modulus values were significantly lower for saturated samples. It was assumed that the existence of water in saturated CSD alters the mechanical response of the material due to the changes in chemical and physical behaviors. These factors are considered to play important roles to decrease the shear strength of CSD. It was proposed that the reduction in CSD shear strength evokes local deformation at the platen-sample boundary, affecting the strength and effective moduli derived from the experiments. The results of this study highlighted the importance of appropriate and consistent testing methods when determining the mechanical

  8. Treating of cement curing with supercritical fluid carbon dioxide

    International Nuclear Information System (INIS)

    The main curing reactions of a portland cement are the formation of portlandite, Ca(OH)2, and calcium silicate hydrates, CSH. In nature, the cement extracts CO2 from air and convert the calcium hydroxide and CSH to calcium carbonate(CaCO3), calcite. By this process, chemically stable and mechanically enhanced cement is formed. By exposing an OPC to supercritical CO2 (SCCO2), the carbonate reaction was greatly accelerated. XRD analysis of experimental sample showed the acceleration of carbonate reaction and the test of compressive strength showed the mechanical enhancement

  9. Influence of calcium sulfoaluminate cement on the pullout performance of reinforcing fibers: An evaluation of the micro-mechanical behavior

    Science.gov (United States)

    Jewell, Robert Benjamin

    The objective of this research was to determine the influence of calcium sulfoaluminate (CSA) cement on reinforcing fibers by evaluating the fiber pullout behavior, and bonding characteristics, of a single fiber embedded in a cementitious paste matrix. Four types of fibers commonly used in industry were evaluated: 1) Polyvinyl alcohol; 2) Polypropylene; 3) Coated Steel; and 4) Plain Steel. Upward trends in energy costs and potential greenhouse gas regulations favor an increased use of construction materials that require lower energy and lower CO2 emissions to fabricate, such as CSA cement, as opposed to the production of ordinary portland cement (OPC), which is more energy intensive and produces more CO2 emissions. However, widespread use of CSA cement requires a more in-depth understanding of the engineering characteristics that govern its performance, including interaction with reinforcing fibers. The overarching objective of this research was to provide the engineering base needed for the utilization of reinforcing fibers in CSA cement-based construction materials. The aims of the research were (1) to develop an ettringite-rich calcium sulfoaluminate cement, and (2) evaluate the pullout characteristics of reinforcing fibers embedded in a CSA-cement matrix. Key elements of the strategy included (1) Compare the performance of a laboratory-fabricated CSA cement to a commercial CSA cement and OPC, (2) Evaluate the peak load, and toughness of reinforcing fibers in CSA cement and OPC, (3) Evaluate the debonding-energy density and multiple-cracking behavior of fibers in CSA cement and OPC, and (4) Evaluate the shear bond strength of reinforcing fibers in CSA cement and OPC. Based on the findings of this PhD dissertation, calcium sulfoaluminate cement has a significant influence on the characteristics and behavior of embedded reinforcing fibers. An important factor contributing to the bond strength between fiber and matrix was the ability to transfer interfacial

  10. Mechanical evaluation of implanted calcium phosphate cement incorporated with PLGA microparticles

    OpenAIRE

    Link, Dennis P.; VAN DEN DOLDER, Juliette; Jurgens, J. F. M.; Wolke, Joop G.; Jansen, John A.

    2006-01-01

    In this study, the mechanical properties of an implanted calcium phosphate (CaP) cement incorporated with 20wt% poly (DL-lactic-coglycolic acid) (PLGA) microparticles were investigated in a rat cranial defect. After 2, 4 and 8 weeks of implantation, implants were evaluated mechanically (push-out test) and morphologically (Scanning Electron Microscopy (SEM) and histology). The results of the push-out test showed that after 2 weeks the shear strength of the implants was 0.4470.44MPa (a...

  11. Photo-luminescent properties of a green or red emitting Tb3+ or Eu3+ doped calcium magnesium silicate phosphors

    International Nuclear Information System (INIS)

    This study describes green-emitting Tb3+ or red-emitting Eu3+ doped calcium magnesium silicate phosphors by ultraviolet excitation at 335 nm. The rare earth activated amorphous calcium silicate was prepared by a solution–combustion process at 600 °C for 5–10 min. The Ca2MgSi2O7 prepared using urea and ammonium nitrate has a tetragonal crystal structure. The resulting Tb3+-doped phosphor emitted green light centered at 544 nm. The optimum excitation wavelength within the range 300–400 nm was 335 nm. The intensity and emitting wavelength of the Eu3+ doped samples can be controlled by annealing in a reducing or oxidizing environment, allowing light to be emitted as green or red. When the reducing environment is optimized, the emission spectrum of Ca2MgSi2O7:Eu2+ is a broad band at 497 nm.

  12. Stabilization of ZnCl2-Containing Waste Using Calcium Sulfoaluminate Cement

    International Nuclear Information System (INIS)

    The potential of calcium sulfoaluminate (CSA) cement was investigated to solidify and stabilize radwastes containing large amounts of soluble zinc chloride (a strong inhibitor of Portland cement hydration). Hydration of pastes and mortars prepared with a 0.5 mol/L ZnCl2 mixing solution was characterized over one year as a function of the gypsum content of the binder and the thermal history of the material. Blending the CSA clinker with 20% gypsum enabled rapid hydration, with only very small delay compared with a reference prepared with pure water. It also improved the compressive strength of the hardened material and significantly reduced its expansion under wet curing. Moreover, the hydrate assemblage was less affected by a thermal treatment at early age simulating the temperature rise and fall occurring in a large-volume drum of cemented waste. Fully hydrated materials contained ettringite, amorphous aluminum hydroxide, straetlingite, together with AFm phases (Kuzel's salt associated with monosulfoaluminate or Friedel's salt depending on the gypsum content of the binder), and possibly C-(A)-S-H. Zinc was readily insolubilized and could not be detected in the pore solution extracted from cement pastes, or in their leachates after 3 months of leaching by pure water at pH 7. The good retention of zinc by the cement matrix was mainly attributed to the precipitation of a hydrated and well crystallized phase with platelet morphology (which may belong to the layered double hydroxides family) at early age ≤ 1 day), and to chemisorption onto aluminum hydroxide at later age. (author)

  13. Biological Assessment of a Calcium Silicate Incorporated Hydroxyapatite-Gelatin Nanocomposite: A Comparison to Decellularized Bone Matrix

    OpenAIRE

    Dong Joon Lee; Ricardo Padilla; He Zhang; Wei-Shou Hu; Ching-Chang Ko

    2014-01-01

    Our laboratory utilized biomimicry to develop a synthetic bone scaffold based on hydroxyapatite-gelatin-calcium silicate (HGCS). Here, we evaluated the potential of HGCS scaffold in bone formation in vivo using the rat calvarial critical-sized defect (CSD). Twelve Sprague-Dawley rats were randomized to four groups: control (defect only), decellularized bone matrix (DECBM), and HGCS with and without multipotent adult progenitor cells (MAPCs). DECBM was prepared by removing all the cells using ...

  14. Effects of graphene plates’ adoption on the microstructure, mechanical properties, and in vivo biocompatibility of calcium silicate coating

    OpenAIRE

    Xie YT; Li HQ; Ding CX; Zheng XB; Li K

    2015-01-01

    Youtao Xie, Hongqin Li, Chuanxian Ding, Xuebin Zheng, Kai Li Shanghai Institute of Ceramics, Key Laboratory of Inorganic Coating Materials, Chinese Academy of Sciences, Shanghai, People’s Republic of China Abstract: Calcium silicate (CS) ceramic is a good coating candidate for biomedical implants to improve biocompatibility and accelerate early osseo-integration. However, the poor fracture toughness and wear resistance of this ceramic material restricts the long-term performance of impl...

  15. A novel titania/calcium silicate hydrate hierarchical coating on titanium.

    Science.gov (United States)

    Huang, Qianli; Liu, Xujie; Elkhooly, Tarek A; Zhang, Ranran; Shen, Zhijian; Feng, Qingling

    2015-10-01

    Recently, surface micron/nano-topographical modifications have attracted a great deal of attention because it is capable of mimicking the hierarchical characteristics of bone. In the current work, a novel titania/calcium silicate hydrate (CSH) bi-layer coating with hierarchical surface topography was successfully prepared on titanium substrate through micro-arc oxidation (MAO) and subsequent hydrothermal treatment (HT). MAO treatment could lead to a micron-scale topographical surface with numerous crater-like protuberances. The subsequent HT process enables the in situ nucleation and growth of CSH nanoplates on MAO-fabricated titania surface. The nucleation of CSH nanoplates is considered to follow a dissolution-precipitation mechanism. Compared to MAO-fabricated coating with single-scale surface topography, MAO-HT-fabricated coating with hierarchical surface topography exhibits enhanced hydrophilicity, fibronectin adsorption and initial MG-63 cell attachment. The process of cell-material interactions is considered to be triggered by surface properties of the coated layer and indirectly mediated by protein adsorption on coating surface. These results suggest that MAO-HT treatment is an efficient way to prepare coatings with hierarchical surface topography on titanium surface, which is essential for altering protein adsorption and initial cell attachment. PMID:26196089

  16. Electrodeposition of porous hydroxyapatite/calcium silicate composite coating on titanium for biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Yong; Han, Shuguang [Institute of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 610054 (China); Pang, Xiaofeng, E-mail: pxf2012@yahoo.com.cn [Institute of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 610054 (China); International Centre for Materials Physics, Chinese Academy of Science, Shenyang 110015 (China); Ding, Qionqion; Yan, Yajing [Institute of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 610054 (China)

    2013-04-15

    A novel method of electrolytic porous hydroxyapatite/calcium silicate (HA/CaSiO{sub 3}) composite coating was conducted on pure titanium in a mixed solution of nano-SiO{sub 2}, Ca(NO{sub 3}){sub 2} and NH{sub 4}H{sub 2}PO{sub 4}. SEM observation showed that the composite layer was porous, thereby providing abundant sites for the osteoblast adhesion. XRD results showed that the composite coating was mainly composed of HA and CaSiO{sub 3}. Bond strength testing exhibited that HA-CaSiO{sub 3}/Ti had higher bond strength than HA/Ti. The HA/CaSiO{sub 3} coating was more corrosion resistant than the HA coating based on the polarization tests. In vitro cell experiments demonstrated that both the HA and HA/CaSiO{sub 3} coatings showed better cell response than the bared titanium. In addition, the proliferation of MC3T3-E1 osteoblast cells grown on the HA/CaSiO{sub 3} coating were remarkably higher than those on the bared Ti and pure HA coating.

  17. Electrodeposition of porous hydroxyapatite/calcium silicate composite coating on titanium for biomedical applications

    Science.gov (United States)

    Huang, Yong; Han, Shuguang; Pang, Xiaofeng; Ding, Qionqion; Yan, Yajing

    2013-04-01

    A novel method of electrolytic porous hydroxyapatite/calcium silicate (HA/CaSiO3) composite coating was conducted on pure titanium in a mixed solution of nano-SiO2, Ca(NO3)2 and NH4H2PO4. SEM observation showed that the composite layer was porous, thereby providing abundant sites for the osteoblast adhesion. XRD results showed that the composite coating was mainly composed of HA and CaSiO3. Bond strength testing exhibited that HA-CaSiO3/Ti had higher bond strength than HA/Ti. The HA/CaSiO3 coating was more corrosion resistant than the HA coating based on the polarization tests. In vitro cell experiments demonstrated that both the HA and HA/CaSiO3 coatings showed better cell response than the bared titanium. In addition, the proliferation of MC3T3-E1 osteoblast cells grown on the HA/CaSiO3 coating were remarkably higher than those on the bared Ti and pure HA coating.

  18. The Performance of Calcium Silicate Board Partition Fireproof Drywall Assembly with Junction Box under Fire

    Directory of Open Access Journals (Sweden)

    Yinuo Wang

    2015-01-01

    Full Text Available This study uses a metal stud partition fireproof drywall measuring 83 mm in thickness as a test specimen to explore the impact of an embedded junction box on the firefighting performance of the wall through one time of standard fire test on a 300 cm × 300 cm area and five times of standard fire test on a 120 cm × 120 cm area. The results show that the quality of calcium silicate board plays a big role in the fireproof effectiveness. The embedded junction box located on the backside of the fire can reduce the effectiveness of the wall, especially the area above the socket. The thickness of rock wool may increase the performance, but in a limited rate. External junction box may not impact the fireproofing performance of the wall but it still possesses some safety risks. An embedded junction box measuring 101 × 55 mm could already damage the fire compartment, and in reality there may be more complicated situations that should be noted and improved.

  19. Combination of simvastatin, calcium silicate/gypsum, and gelatin and bone regeneration in rabbit calvarial defects

    Science.gov (United States)

    Zhang, Jing; Wang, Huiming; Shi, Jue; Wang, Ying; Lai, Kaichen; Yang, Xianyan; Chen, Xiaoyi; Yang, Guoli

    2016-03-01

    The present study was performed to determine whether simvastatin improves bone regeneration when combined with calcium silicate/gypsum and gelatin (CS-GEL). The surface morphology was determined using field-emission scanning electron microscopy (FSEM). Degradation in vitro was evaluated by monitoring the weight change of the composites soaked in phosphate buffered saline (PBS). Drug release was evaluated using high-performance liquid chromatography (HPLC). Cytotoxicity testing was performed to assess the biocompatibility of composites. Four 5 mm-diameter bone defects were created in rabbit calvaria. Three sites were filled with CS-GEL, 0.5 mg simvastatin-loaded CS-GEL (SIM-0.5) and 1.0 mg simvastatin-loaded CS-GEL (SIM-1.0), respectively, and the fourth was left empty as the control group. Micro-computed tomography (micro-CT) and histological analysis were carried out at 4 and 12 weeks postoperatively. The composites all exhibited three-dimensional structures and showed the residue with nearly 80% after 4 weeks of immersion. Drug release was explosive on the first day and then the release rate remained stable. The composites did not induce any cytotoxicity. The results in vivo demonstrated that the new bone formation and the expressions of BMP-2, OC and type I collagen were improved in the simvastatin-loaded CS-GEL group. It was concluded that the simvastatin-loaded CS-GEL may improve bone regeneration.

  20. Mechanical and microstructure of reinforced hydroxyapatite/calcium silicate nano-composites materials

    International Nuclear Information System (INIS)

    Highlights: ► Nano sized of HA and CS powders were prepared. ► Mechanical of HACS composites enhanced with content of CS. ► The apatite formation onto the composites is proved. -- Abstract: In this study, the nano sized hydroxyapatite (HA) and calcium silicate (CS) powders prepared by both chemical precipitation and sol–gel methods respectively. Biphasic nano-composites materials containing different ratios of HA and CS were fabricated and assessed using X-ray diffraction (XRD), Fourier transmission infrared reflectance (FT-IR), transmission electron microscopy (TEM) and scanning electron microscopy (SEM) techniques. The effect of variation of ratios between HA and CS on mechanical properties, microstructure and in vitro study was studied. The results proved that the mechanical properties were enhanced with increasing the CS ratio in the composite. In vitro study proved the formation and nucleation of apatite onto composites surfaces which contain low content of CS after one week of immersion. Finally, it is concluded that the HACS composites containing high HA content at the expense of CS content will be promising for bone substitute’s applications, especially in load bearing sites.

  1. Low-to-Medium-Frequency AC Impedance Spectroscopy Investigations of Nanocrystalline Calcium Silicate Hydrate Dried Powders

    International Nuclear Information System (INIS)

    Low-to-medium-frequency range impedance spectroscopy was used to investigate two series of dried calcium silicate hydrates with or without aluminum atoms, C-S-H and C-A-S-H. Over four decades in frequency, sample Nyquist plots were fitted by adopting an equivalent circuit using constant phase elements (CPE). Conductivity values of the order of 10-9-10-10 S/cm were obtained at 316 K. The presence of CPE characteristic of the depleted semicircle at high frequency was related to a fractal dimension ranging from 2.4 up to 2.7. Above 316 K, the impedance spectra behaved unpredictably due to the dehydration process, while below 316 K the behavior was followed by adopting the modulus loss factor. The associated peak maximum variation is of the Arrhenius-type. The entire behavior may be interpreted by ionic motion and charge accumulation in addition to dielectric polarization at the grain boundaries associated to low fractal surface. (authors)

  2. Electrodeposition of porous hydroxyapatite/calcium silicate composite coating on titanium for biomedical applications

    International Nuclear Information System (INIS)

    A novel method of electrolytic porous hydroxyapatite/calcium silicate (HA/CaSiO3) composite coating was conducted on pure titanium in a mixed solution of nano-SiO2, Ca(NO3)2 and NH4H2PO4. SEM observation showed that the composite layer was porous, thereby providing abundant sites for the osteoblast adhesion. XRD results showed that the composite coating was mainly composed of HA and CaSiO3. Bond strength testing exhibited that HA-CaSiO3/Ti had higher bond strength than HA/Ti. The HA/CaSiO3 coating was more corrosion resistant than the HA coating based on the polarization tests. In vitro cell experiments demonstrated that both the HA and HA/CaSiO3 coatings showed better cell response than the bared titanium. In addition, the proliferation of MC3T3-E1 osteoblast cells grown on the HA/CaSiO3 coating were remarkably higher than those on the bared Ti and pure HA coating.

  3. Combination of simvastatin, calcium silicate/gypsum, and gelatin and bone regeneration in rabbit calvarial defects.

    Science.gov (United States)

    Zhang, Jing; Wang, Huiming; Shi, Jue; Wang, Ying; Lai, Kaichen; Yang, Xianyan; Chen, Xiaoyi; Yang, Guoli

    2016-01-01

    The present study was performed to determine whether simvastatin improves bone regeneration when combined with calcium silicate/gypsum and gelatin (CS-GEL). The surface morphology was determined using field-emission scanning electron microscopy (FSEM). Degradation in vitro was evaluated by monitoring the weight change of the composites soaked in phosphate buffered saline (PBS). Drug release was evaluated using high-performance liquid chromatography (HPLC). Cytotoxicity testing was performed to assess the biocompatibility of composites. Four 5 mm-diameter bone defects were created in rabbit calvaria. Three sites were filled with CS-GEL, 0.5 mg simvastatin-loaded CS-GEL (SIM-0.5) and 1.0 mg simvastatin-loaded CS-GEL (SIM-1.0), respectively, and the fourth was left empty as the control group. Micro-computed tomography (micro-CT) and histological analysis were carried out at 4 and 12 weeks postoperatively. The composites all exhibited three-dimensional structures and showed the residue with nearly 80% after 4 weeks of immersion. Drug release was explosive on the first day and then the release rate remained stable. The composites did not induce any cytotoxicity. The results in vivo demonstrated that the new bone formation and the expressions of BMP-2, OC and type I collagen were improved in the simvastatin-loaded CS-GEL group. It was concluded that the simvastatin-loaded CS-GEL may improve bone regeneration. PMID:26996657

  4. In situ hydroxyapatite nanofiber growth on calcium borate silicate ceramics in SBF and its structural characteristics.

    Science.gov (United States)

    Pu, Yinfu; Huang, Yanlin; Qi, Shuyun; Chen, Cuili; Seo, Hyo Jin

    2015-10-01

    A novel calcium silicate borate Ca11Si4B2O22 ceramic was firstly prepared by the conventional solid-state reaction. In vitro hydroxyapatite mineralization was investigated by soaking the ceramics in simulated body fluid (SBF) solutions at body temperature (37 °C) for various time periods. Scanning electron microscopy (SEM) and X-ray diffraction analysis (XRD) measurements were applied to investigate the samples before and after the immersion of ceramics in SBF solution. The elemental compositions of a hydroxyapatite layer on the ceramics during the mineralization were confirmed by X-ray energy-dispersive spectra (EDS). Meanwhile, the bending strength and elastic modulus of Ca11Si4B2O22 ceramics were also measured, which indicate that the biomaterials based on Ca11Si4B2O22 ceramics possess bioactivity and might be a potential candidate as biomaterials for hard tissue repair. The bioactive mineralization ability was evaluated on the base of its crystal structural characteristics, i.e., silanol (Si-OH) and B-OH groups can be easily induced on the surface of Ca11Si4B2O22 ceramics soaked in SBF solutions. PMID:26117746

  5. Preparation and characterization of high-strength calcium silicate boards from coal-fired industrial solid wastes

    Institute of Scientific and Technical Information of China (English)

    Zhao Cao; Yong-dan Cao; Jin-shan Zhang; Chun-bao Sun; Xian-long Li

    2015-01-01

    To realize the comprehensive utilization of coal-fired industrial solid wastes, a novel high-strength board was prepared from cal-cium silicate slag, fly ash, and flue gas desulfurization (FGD) gypsum. The changes in mineral phases, chemical structure, and morphology during hydration were investigated by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron mi-croscopy (SEM). A traditional board made from quartz and lime was prepared as a reference. The novel board not only consumes a lot of solid wastes, but also meets the strength requirement of the class-five calcium silicate board according to the Chinese Standard JC/T 564.2—2008. Microanalysis showed that hydrated calcium silicate gel (C−S−H(I)), ettringite, tobermorite, and xonotlite were successivelygenerated in the novel board by synergistic hydration of the mixed solid wastes. The board strength was improved by the formation of tobermorite and xonotlite but decreased by unhydrated quartz. It was demonstrated that quartz was not completely hydrated in the traditional board. As a re-sult, the flexural strength of the traditional board was much lower than that of the novel board.

  6. Preliminary study of raw material for calcium silicate/PVA coating on Ti-6Al-4V alloy

    International Nuclear Information System (INIS)

    Calcium silicate bioceramic was prepared from the rice husk and limestone resources using the sol gel method. The preparations of CaSiO3 formulation were differ from the previous study due CaO/SiO2 amount with 45:55 ratio. X-Ray Fluorescence analysis was carried out to clarify the amount of SiO2 and CaO content in the limestone and rice husk ash. The high amount of CaO was found in the limestone with the percentages of 97.22%, whereby 89% of SiO2 content of the rice husk ash. Several milling time were studied to obtain the optimized milling ti me and speed in progress to obtain nano size particle. The particle size analysis result confirms that increase in milling time does not certainly reduce the size of particle. The addition of 0.05% polyvinyl alcohol as a binder did not change the phases or composition of calcium silicates after examined by X-Ray diffraction analysis which make it suitable to be used as a binder for calcium silicate coating without changing the chemical structure

  7. Preparation and characterization of high-strength calcium silicate boards from coal-fired industrial solid wastes

    Science.gov (United States)

    Cao, Zhao; Cao, Yong-dan; Zhang, Jin-shan; Sun, Chun-bao; Li, Xian-long

    2015-08-01

    To realize the comprehensive utilization of coal-fired industrial solid wastes, a novel high-strength board was prepared from calcium silicate slag, fly ash, and flue gas desulfurization (FGD) gypsum. The changes in mineral phases, chemical structure, and morphology during hydration were investigated by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). A traditional board made from quartz and lime was prepared as a reference. The novel board not only consumes a lot of solid wastes, but also meets the strength requirement of the class-five calcium silicate board according to the Chinese Standard JC/T 564.2—2008. Microanalysis showed that hydrated calcium silicate gel (C-S-H(I)), ettringite, tobermorite, and xonotlite were successively generated in the novel board by synergistic hydration of the mixed solid wastes. The board strength was improved by the formation of tobermorite and xonotlite but decreased by unhydrated quartz. It was demonstrated that quartz was not completely hydrated in the traditional board. As a result, the flexural strength of the traditional board was much lower than that of the novel board.

  8. Effects of Zn Content on Crystal Structure, Cytocompatibility, Antibacterial Activity, and Chemical Stability in Zn-Modified Calcium Silicate Coatings

    Science.gov (United States)

    Li, Kai; Yu, Jiangming; Xie, Youtao; Huang, Liping; Ye, Xiaojian; Zheng, Xuebin

    2013-08-01

    In our previous study, Zn-modified calcium silicate coatings possess not only excellent chemical stability but also well antibacterial activity. Still, effects of zinc content on these properties and cytocompatibility remain unclear. In this paper, two kinds of Zn-modified calcium silicate coatings (ZC0.3, ZC0.5) were fabricated on Ti-6Al-4V substrates via plasma spraying technology. X-ray diffraction results and transmission electron microscopy observations showed that the ZC0.5 coating was composed of pure hardystonite (Ca2ZnSi2O7) phase, while, besides Ca2ZnSi2O7 phase, the amorphous CaSiO3 phase was also detected in the ZC0.3 coating. Chemical stability in Tris-HCl buffer solution and antibacterial activity of the Zn-modified calcium silicate coatings increased with an increase in zinc content. In vitro cytocompatibility evaluation demonstrated that the proliferation and alkaline phosphatase activity and collagen type I (COLI) secretion of osteoblast-like MC3T3-E1 cells on Zn-modified coatings were significantly enhanced compared to the Zn-free coating and Ti-6Al-4V control, and no cytotoxicity appeared on Zn-modified coatings. The better antibacterial activity and the enhanced capability to promote MC3T3-E1 cells differentiation of Zn-modified coatings should be attributed to the slow and constant Zn2+ releasing from the coatings.

  9. Preliminary study of raw material for calcium silicate/PVA coating on Ti-6Al-4V alloy

    Energy Technology Data Exchange (ETDEWEB)

    Azam, Farah ' Atiqah bt Abdul; Shamsudin, Roslinda, E-mail: linda@ukm.edu.my [School of Applied Physics, Faculty of Science and Technology Universiti Kebangsaan Malaysia, 43600 UKM Bangi, Selangor Darul Ehsan (Malaysia)

    2015-09-25

    Calcium silicate bioceramic was prepared from the rice husk and limestone resources using the sol gel method. The preparations of CaSiO{sub 3} formulation were differ from the previous study due CaO/SiO{sub 2} amount with 45:55 ratio. X-Ray Fluorescence analysis was carried out to clarify the amount of SiO{sub 2} and CaO content in the limestone and rice husk ash. The high amount of CaO was found in the limestone with the percentages of 97.22%, whereby 89% of SiO{sub 2} content of the rice husk ash. Several milling time were studied to obtain the optimized milling ti me and speed in progress to obtain nano size particle. The particle size analysis result confirms that increase in milling time does not certainly reduce the size of particle. The addition of 0.05% polyvinyl alcohol as a binder did not change the phases or composition of calcium silicates after examined by X-Ray diffraction analysis which make it suitable to be used as a binder for calcium silicate coating without changing the chemical structure.

  10. Preliminary study of raw material for calcium silicate/PVA coating on Ti-6Al-4V alloy

    Science.gov (United States)

    Azam, Farah Atiqah bt Abdul; Shamsudin, Roslinda

    2015-09-01

    Calcium silicate bioceramic was prepared from the rice husk and limestone resources using the sol gel method. The preparations of CaSiO3 formulation were differ from the previous study due CaO/SiO2 amount with 45:55 ratio. X-Ray Fluorescence analysis was carried out to clarify the amount of SiO2 and CaO content in the limestone and rice husk ash. The high amount of CaO was found in the limestone with the percentages of 97.22%, whereby 89% of SiO2 content of the rice husk ash. Several milling time were studied to obtain the optimized milling ti me and speed in progress to obtain nano size particle. The particle size analysis result confirms that increase in milling time does not certainly reduce the size of particle. The addition of 0.05% polyvinyl alcohol as a binder did not change the phases or composition of calcium silicates after examined by X-Ray diffraction analysis which make it suitable to be used as a binder for calcium silicate coating without changing the chemical structure.

  11. Improved workability of injectable calcium sulfate bone cement by regulation of self-setting properties

    International Nuclear Information System (INIS)

    Calcium sulfate hemihydrate (CSH) powder as an injectable bone cement was prepared by hydrothermal synthesis of calcium sulfate dihydrate (CSD). The prepared materials showed X-ray diffraction peaks corresponding to the CSH structure without any secondary phases, implying complete conversion from CSD phase to CSH phase. Thermogravimetric (TG) analyses showed the crystal water content of CSH was about 6.0% (wt.), which is near to the theoretic crystal water value of CSH. From scanning electron microscopy (SEM) micrographs, sheet crystal structure of CSD was observed to transform into rod-like crystal structure of CSH. Most interesting and important of all, CSD as setting accelerator was also introduced into CSH powder to regulate self-setting properties of injectable CSH paste, and thus the self-setting time of CSH paste can be regulated from near 30 min to less than 5 min by adding various amounts of setting accelerator. Because CSD is not only the reactant of preparing CSH but also the final solidified product of CSH, the setting accelerator has no significant effect on the other properties of materials, such as mechanical properties. In vitro biocompatibility and in vivo histology studies have demonstrated that the materials have good biocompatibility and good efficacy in bone regeneration. All these will further improve the workability of CSH in clinic applications. Highlights: ► Calcium sulfate hemihydrate (CSH) can be an injectable bone cement. ► CSH was produced by hydrothermal synthesis of calcium sulfate dihydrate (CSD). ► CSD was introduced into CSH powder to regulate self-setting properties of CSH. ► Setting accelerator has no significant effect on the other properties of materials. ► Injectable CSH has good biocompatibility and good efficacy in bone regeneration

  12. Improved workability of injectable calcium sulfate bone cement by regulation of self-setting properties

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Zonggang, E-mail: chenzg@sdu.edu.cn [National Glycoengineering Research Center, Shandong University, Jinan 250100 (China); Department of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China); Liu, Huanye [Department of Orthodontics, School of Stomatology, China Medical University, Shenyang 110001 (China); Liu, Xi [Department of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China); Lian, Xiaojie [College of Mechanics, Taiyuan University of Technology, Taiyuan 030024 (China); Guo, Zhongwu [National Glycoengineering Research Center, Shandong University, Jinan 250100 (China); Jiang, Hong-Jiang [Wendeng Hospital of Traditional Chinese Orthopedics and Traumatology, Shandong 264400 (China); Cui, Fu-Zhai, E-mail: cuifz@mail.tsinghua.edu.cn [Department of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China)

    2013-04-01

    Calcium sulfate hemihydrate (CSH) powder as an injectable bone cement was prepared by hydrothermal synthesis of calcium sulfate dihydrate (CSD). The prepared materials showed X-ray diffraction peaks corresponding to the CSH structure without any secondary phases, implying complete conversion from CSD phase to CSH phase. Thermogravimetric (TG) analyses showed the crystal water content of CSH was about 6.0% (wt.), which is near to the theoretic crystal water value of CSH. From scanning electron microscopy (SEM) micrographs, sheet crystal structure of CSD was observed to transform into rod-like crystal structure of CSH. Most interesting and important of all, CSD as setting accelerator was also introduced into CSH powder to regulate self-setting properties of injectable CSH paste, and thus the self-setting time of CSH paste can be regulated from near 30 min to less than 5 min by adding various amounts of setting accelerator. Because CSD is not only the reactant of preparing CSH but also the final solidified product of CSH, the setting accelerator has no significant effect on the other properties of materials, such as mechanical properties. In vitro biocompatibility and in vivo histology studies have demonstrated that the materials have good biocompatibility and good efficacy in bone regeneration. All these will further improve the workability of CSH in clinic applications. Highlights: ► Calcium sulfate hemihydrate (CSH) can be an injectable bone cement. ► CSH was produced by hydrothermal synthesis of calcium sulfate dihydrate (CSD). ► CSD was introduced into CSH powder to regulate self-setting properties of CSH. ► Setting accelerator has no significant effect on the other properties of materials. ► Injectable CSH has good biocompatibility and good efficacy in bone regeneration.

  13. The effect of calcium ions and sodium silicate on the adsorption of a model anionic flotation collector on magnetite studied by ATR-FTIR spectroscopy.

    Science.gov (United States)

    Potapova, E; Grahn, M; Holmgren, A; Hedlund, J

    2010-05-01

    Previous studies have shown that agglomeration of the magnetite concentrate after reverse flotation of apatite is negatively affected by the collector species adsorbed on the surface of magnetite. In this work, the effect of ionic strength, calcium ions and sodium silicate on the unwanted adsorption of a model anionic flotation collector on synthetic magnetite was studied in situ using attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR). The amount of collector adsorbed was found to increase with increasing ionic strength at pH 8.5 providing evidence to the contribution of electrostatic forces to the adsorption of the collector. Adding sodium silicate to the system resulted in a threefold decrease in the amount of collector adsorbed compared to when no sodium silicate was added, confirming the depressing activity of sodium silicate on magnetite. Calcium ions were shown to increase the adsorption of both the collector and sodium silicate on magnetite. The depressing effect of sodium silicate on collector adsorption was completely suppressed in the presence of calcium ions under the conditions studied. Furthermore, the amount of collector adsorbed on magnetite from the silicate-collector solution increased 14 times upon addition of calcium ions suggesting that calcium ions in the process water may increase undesired adsorption of the collector on the iron oxide. PMID:20153478

  14. Calcium phosphate cement reinforcement by polymer infiltration and in situ curing: a method for 3D scaffold reinforcement.

    Science.gov (United States)

    Alge, Daniel L; Chu, Tien-Min Gabriel

    2010-08-01

    This study describes a novel method of calcium phosphate cement reinforcement based on infiltrating a pre-set cement with a reactive polymer and then cross-linking the polymer in situ. This method can be used to reinforce 3D calcium phosphate cement scaffolds, which we demonstrate using poly(ethylene glycol) diacrylate (PEGDA) as a model reinforcing polymer. The compressive strength of a 3D scaffold comprised of orthogonally intersecting beams was increased from 0.31 +/- 0.06 MPa to 1.65 +/- 0.13 MPa using PEGDA 600. In addition, the mechanical properties of reinforced cement were characterized using three PEGDA molecular weights (200, 400, and 600 Da) and three cement powder to liquid (P/L) ratios (0.8, 1.0, and 1.43). Higher molecular weight increased reinforcement efficacy, and P/L controlled cement porosity and determined the extent of polymer incorporation. Although increasing polymer incorporation resulted in a transition from brittle, cement-like behavior to ductile, polymer-like behavior, maximizing polymer incorporation was not advantageous. Polymerization shrinkage produced microcracks in the cement, which reduced the mechanical properties. The most effective reinforcement was achieved with P/L of 1.43 and PEGDA 600. In this group, flexural strength increased from 0.44 +/- 0.12 MPa to 7.04 +/- 0.51 MPa, maximum displacement from 0.05 +/- 0.01 mm to 1.44 +/- 0.17 mm, and work of fracture from 0.64 +/- 0.10 J/m(2) to 677.96 +/- 70.88 J/m(2) compared to non-reinforced controls. These results demonstrate the effectiveness of our novel reinforcement method, as well as its potential for fabricating reinforced 3D calcium phosphate cement scaffolds useful for bone tissue engineering. PMID:20186776

  15. Formation of interconnected macropores in apatitic calcium phosphate bone cement with the use of an effervescent additive.

    Science.gov (United States)

    Hesaraki, S; Moztarzadeh, F; Sharifi, D

    2007-10-01

    Calcium phosphate cements (CPCs) can be considered as good candidate for bone tissue engineering because they can be resorbed and take part in the bone remodeling process. Several efforts have been made into improve the resorption rate of the calcium phosphate cement by introducing macropores to the cement matrix. In this investigation a simple and effective method has been presented based on the addition of various amounts of an effervescent agent to the calcium phosphate cement components. The effervescent agent was a mixture of sodium hydrogen carbonate, NaHCO(3) (that was added to the powder phase), and citric acid monohydrate, C(6)H(8)O(7).H(2)O (that was dissolved in the liquid phase). The obtained macroporous samples were characterized by Fourier transform infrared spectrometer, X-ray diffraction, and scanning electron microscopy techniques at 4 h after setting and 3 days after soaking in a special simulated body fluid solution named Hank's balanced salt solution. Mercury intrusion porosimetry was also employed for characterizing the pore volume and pore size distribution in the cement structure. Results showed that the rate of conversion of staring reactant to the apatite phase and the apatite chemistry were significantly changed by using the additive in the cement components. Also both the pore volume and pore size were changed by varying both the amount of effervescent additive and the powder to liquid ratio. PMID:17380498

  16. Use of industrial byproducts as alumina sources for the synthesis of calcium sulfoaluminate cements.

    Science.gov (United States)

    Pace, Maria Lucia; Telesca, Antonio; Marroccoli, Milena; Valenti, Gian Lorenzo

    2011-07-15

    Calcium sulfoaluminate (CSA) cements show some desirable environmentally friendly features that include the possibility of using several industrial byproducts as raw materials in their manufacturing process. Alumina powder, from the secondary aluminum manufacture, and anodization mud, from the production process of anodized aluminum, have proved to be suitable as partial or total substitutes for an expensive natural material like bauxite. CSA clinker generating raw mixtures, containing limestone, natural gypsum, bauxite, and/or one of the alumina-rich byproducts, were heated 2 h in a laboratory electric oven at temperatures ranging from 1150 to 1300 °C. Conversion of reactants into 4CaO·3Al(2)O(3)·SO(3) (the key component of CSA cements), evaluated using X-ray diffraction (XRD) analysis, increased with an increase of both burning temperature and byproduct concentration. When examined through differential thermogravimetric and XRD analyses, a synthetic CSA clinker (made from the raw mixture incorporating alumina powder as a total replacement of bauxite) mixed with 20% gypsum showed a hydration behavior almost similar to that of an industrial CSA cement containing the same amount of gypsum. PMID:21707122

  17. A histological evaluation on osteogenesis and resorption of methotrexate-loaded calcium phosphate cement in vivo

    International Nuclear Information System (INIS)

    In this study, we investigated the resorption of in vivo methotrexate-loaded calcium phosphate cement (MTX-CPC) implants and their effect on osteogenesis. MTX-CPC implants containing 1% methotrexate (MTX) (weight/weight) were preset and implanted into the femoral condyle of rabbits. Calcium phosphate cement (CPC) without MTX was used as the control. The femurs were harvested at day 1 and at 1, 3 and 6 months after implantation and radiological examination were performed. Decalcified sections were examined by hematoxylin and eosin (HE) staining, alkaline phosphatase (ALPase) immunohistochemistry and tartrate-resistant acid phosphatase (TRAPase) enzyme histochemistry. Then, we performed histomorphometric analysis, including determination of the percentage of newly formed bone and osteoblast and osteoclast counts. The results indicated that MTX-CPC implants were biocompatible, biodegradable and osteoconducive. However, MTX release from the implantation site inhibited osteogenesis in the initial period; this inhibition weakened with time, and no difference was observed between CPC and MTX-CPC at 6 months after implantation. Hence, MTX-CPC is an excellent material for filling defects and can be used for preparing effective drug delivery systems to achieve local control of invasive bone tumors.

  18. A histological evaluation on osteogenesis and resorption of methotrexate-loaded calcium phosphate cement in vivo

    Energy Technology Data Exchange (ETDEWEB)

    Li Dong; Yang Zhiping; Li Xin; Li Zhenfeng; Li Jianmin [Department of Orthopedics, Qilu Hospital of Shandong University, Shandong (China); Yang Jingyan, E-mail: yangzhiping@medmail.com.c [Department of Pathology, 2nd Affiliated Hospital of Shandong University, Shandong (China)

    2010-04-15

    In this study, we investigated the resorption of in vivo methotrexate-loaded calcium phosphate cement (MTX-CPC) implants and their effect on osteogenesis. MTX-CPC implants containing 1% methotrexate (MTX) (weight/weight) were preset and implanted into the femoral condyle of rabbits. Calcium phosphate cement (CPC) without MTX was used as the control. The femurs were harvested at day 1 and at 1, 3 and 6 months after implantation and radiological examination were performed. Decalcified sections were examined by hematoxylin and eosin (HE) staining, alkaline phosphatase (ALPase) immunohistochemistry and tartrate-resistant acid phosphatase (TRAPase) enzyme histochemistry. Then, we performed histomorphometric analysis, including determination of the percentage of newly formed bone and osteoblast and osteoclast counts. The results indicated that MTX-CPC implants were biocompatible, biodegradable and osteoconducive. However, MTX release from the implantation site inhibited osteogenesis in the initial period; this inhibition weakened with time, and no difference was observed between CPC and MTX-CPC at 6 months after implantation. Hence, MTX-CPC is an excellent material for filling defects and can be used for preparing effective drug delivery systems to achieve local control of invasive bone tumors.

  19. Bioactive calcium sulfate/magnesium phosphate cement for bone substitute applications

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Guangyong [Department of Orthopaedics, Taizhou Hospital of Zhejiang Province, Linhai Zhejiang, 317000 (China); Department of Orthopaedic Surgery, Second Affiliated Hospital of Wenzhou Medical College, Wenzhou, Zhejiang, 325000 (China); Liu, Jianli [Trauma Center, Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 570206 (China); Division of Functional Materials and Nanodevices, Ningbo Institute of Materials Technology and Engineering (NIMTE), Chinese Academy of Sciences (CAS), Ningbo, Zhejiang, 315201 (China); Li, Fan; Pan, Zongyou; Ni, Xiao; Shen, Yue [Department of Orthopaedic Surgery, Second Affiliated Hospital of Wenzhou Medical College, Wenzhou, Zhejiang, 325000 (China); Xu, Huazi, E-mail: spinexu@163.com [Department of Orthopaedic Surgery, Second Affiliated Hospital of Wenzhou Medical College, Wenzhou, Zhejiang, 325000 (China); Huang, Qing, E-mail: huangqing@nimte.ac.cn [Division of Functional Materials and Nanodevices, Ningbo Institute of Materials Technology and Engineering (NIMTE), Chinese Academy of Sciences (CAS), Ningbo, Zhejiang, 315201 (China)

    2014-02-01

    A novel calcium sulfate/magnesium phosphate cement (CSMPC) composite was prepared and studied in the present work. The physical properties including the phases, the microstructures, the setting properties and the compressive strengths of the CSMPCs were studied. The bio-performances of the CSMPCs were comprehensively evaluated using in vitro simulated body fluid (SBF) method and in vitro cell culture. The dependence of the physical and chemical properties of the CSMPC on its composition and microstructure was studied in detail. It is found that the CSMPC composites exhibited mediate setting times (6–12 min) compared to the calcium sulfate (CS) and the magnesium phosphate cement (MPC). They showed an encapsulation structure in which the unconverted hexagonal prism CSH particles were embedded in the xerogel-like MPC matrix. The phase compositions and the mechanical properties of the CSMPCs were closely related to the content of MPC and the hardening process. The CSMPCs exhibited excellent bioactivity and good biocompatibility to support the cells to attach and proliferate on the surface. The CSMPC composite has the potential to serve as bone grafts for the bone regeneration. - Highlights: • The mechanical strength and degradation rate of CSMPC composites are discussed. • The CSMPC composites exhibited good bioactivity to form bone-like apatite. • The CSMPC composites also show good biocompatibility.

  20. Bioactive calcium sulfate/magnesium phosphate cement for bone substitute applications

    International Nuclear Information System (INIS)

    A novel calcium sulfate/magnesium phosphate cement (CSMPC) composite was prepared and studied in the present work. The physical properties including the phases, the microstructures, the setting properties and the compressive strengths of the CSMPCs were studied. The bio-performances of the CSMPCs were comprehensively evaluated using in vitro simulated body fluid (SBF) method and in vitro cell culture. The dependence of the physical and chemical properties of the CSMPC on its composition and microstructure was studied in detail. It is found that the CSMPC composites exhibited mediate setting times (6–12 min) compared to the calcium sulfate (CS) and the magnesium phosphate cement (MPC). They showed an encapsulation structure in which the unconverted hexagonal prism CSH particles were embedded in the xerogel-like MPC matrix. The phase compositions and the mechanical properties of the CSMPCs were closely related to the content of MPC and the hardening process. The CSMPCs exhibited excellent bioactivity and good biocompatibility to support the cells to attach and proliferate on the surface. The CSMPC composite has the potential to serve as bone grafts for the bone regeneration. - Highlights: • The mechanical strength and degradation rate of CSMPC composites are discussed. • The CSMPC composites exhibited good bioactivity to form bone-like apatite. • The CSMPC composites also show good biocompatibility

  1. X-AFm stabilization as a mechanism of bypassing conversion phenomena in calcium aluminate cements

    International Nuclear Information System (INIS)

    Phase conversion phenomena are often observed in calcium aluminate cements (CACs), when the water-rich hydrates (e.g., CAH10, C2AH8) formed at early ages, at temperatures ≤ 30 °C, expel water in time to form more compact, less water-rich structures (C3AH6). The phase conversions follow a path regulated by the thermodynamic stabilities (solubilities) of phases. Based on this premise, it is proposed that conversion phenomena in CACs can be bypassed by provoking the precipitation of phases more preferred than those typically encountered along the conversion pathway. Therefore, X-AFm formation (where in this case, X = NO3−) triggered by the sequential addition of calcium nitrate (Ca(NO3)2 = CN) additives is identified as a new means of bypassing conversion. A multi-method approach comprising X-ray diffraction (XRD), thermal analytics, and evaluations of the compressive strength is applied to correlate phase balances and properties of CAC systems cured at 25 °C and 45 °C. The results highlight the absence of the C3AH6 phase across all systems and the curing conditions considered, with enhanced strengths being noted, when sufficient quantities of CN are added. The experimental outcomes are supported by insights gained from thermodynamic calculations which highlight thermodynamic selectivity as a means of regulating and controlling the evolutions of solid phase balances using inorganic salts in CACs, and more generally in cementing material systems

  2. Conservative Management of Class 4 Invasive Cervical Root Resorption Using Calcium-enriched Mixture Cement.

    Science.gov (United States)

    Asgary, Saeed; Nosrat, Ali

    2016-08-01

    Class 4 invasive cervical root resorption (ICRR) presents a treatment dilemma in endodontics. The widely accepted treatment options for a class 4 ICRR are to leave these teeth untreated for as long as they are asymptomatic or extraction. This report presents a conservative approach for the management of class 4 ICRR. A 28-year-old woman was referred for root canal treatment of tooth #26. The patient had a history of orthodontic treatment. Radiographic evaluation showed class 4 ICRR that had perforated the root canal space, a radiolucent crestal bony defect, and a periapical lesion. Clinically, a deep (6-mm) probing area was found on the mesial side of the tooth that bled on probing. The tooth was sensitive to percussion. After the treatment options were discussed with the patient, she chose to save the tooth. After complete chemomechanical preparation of the root canal, the entire canal space and perforation area were filled with calcium-enriched mixture cement. No attempt was made to mechanically remove the resorptive lacuna. Twenty four months after treatment, the tooth was functional and asymptomatic, and probing was within normal limits (canal space with calcium-enriched mixture cement may be a viable treatment option for an otherwise non-treatable tooth with class 4 invasive cervical root resorption. PMID:27316319

  3. Silicon-stabilized α-tricalcium phosphate and its use in a calcium phosphate cement: characterization and cell response.

    Science.gov (United States)

    Mestres, Gemma; Le Van, Clemence; Ginebra, Maria-Pau

    2012-03-01

    α-Tricalcium phosphate (α-TCP) is widely used as a reactant in calcium phosphate cements. This work aims at doping α-TCP with silicon with a twofold objective. On the one hand, to study the effect of Si addition on the stability and reactivity of this polymorph. On the other, to develop Si-doped cements and to evaluate the effect of Si on their in vitro cell response. For this purpose a calcium-deficient hydroxyapatite was sintered at 1250°C with different amounts of silicon oxide. The high temperature polymorph α-TCP was stabilized by the presence of silicon, which inhibited reversion of the β→α transformation, whereas in the Si-free sample α-TCP completely reverted to the β-polymorph. However, the β-α transformation temperature was not affected by the presence of Si. Si-α-TCP and its Si-free counterpart were used as reactants for a calcium phosphate cement. While Si-α-TCP showed faster hydrolysis to calcium-deficient hydroxyapatite, upon complete reaction the crystalline phases, morphology and mechanical properties of both cements were similar. An in vitro cell culture study, in which osteoblast-like cells were exposed to the ions released by both materials, showed a delay in cell proliferation in both cases and stimulation of cell differentiation, more marked for the Si-containing cement. These results can be attributed to strong modification of the ionic concentrations in the culture medium by both materials. Ca-depletion from the medium was observed for both cements, whereas continuous Si release was detected for the Si-containing cement. PMID:22154863

  4. Characterization of high-calcium fly ash and its influence on ettringite formation in portland cement pastes

    Science.gov (United States)

    Tishmack, Jody Kathleen

    High-calcium Class C fly ashes derived from Powder River Basin coal are currently used as supplementary cementing materials in portland cement concrete. These fly ashes tend to contain significant amounts of sulfur, calcium, and aluminum, thus they are potential sources of ettringite. Characterization of six high-calcium fly ashes originating from Powder River Basin coal have been carried out. The hydration products formed in pastes made from fly ash and water were investigated. The principal phases produced at room temperature were ettringite, monosulfate, and stratlingite. The relative amounts formed varied with the specific fly ash. Removal of the soluble crystalline sulfur bearing minerals indicated that approximately a third of the sulfur is located in the fly ash glass. Pore solution analyses indicated that sulfur concentrations increased at later ages. Three fly ashes were selected for further study based on their ability to form ettringite. Portland cement-fly ash pastes made with the selected fly ashes were investigated to evaluate ettringite and monosulfate formation. Each of the fly ashes were mixed with four different types of portland cements (Type I, I/II, II, and III) as well as three different Type I cements exhibiting a range of C3A and sulfate contents. The pastes had 25% or 35% fly ash by total weight of solids and a water:cement-fly ash ratio of 0.45. The samples were placed in a curing room (R.H. = 100, 23°C) and were then analyzed at various ages by x-ray diffraction (XRD) and differential scanning calorimetry (DSC) to determine the principal hydration products. The hydration products identified by XRD were portlandite, ettringite (an AFt phase), monosulfate, and generally smaller amounts of hemicarboaluminate and monocarboaluminate (all AFm phases). Although the amount of ettringite formed varied with the individual cement, only a modest correlation with cement sulfate content and no correlation with cement C3A content was observed. DSC

  5. Effect of calcium silicate slag application on radium-226 concentrations in plant tissues

    International Nuclear Information System (INIS)

    A greenhouse pot experiment was conducted to determine if plants absorb Ra from slag applied to soil. Slag at rates equivalent to 0 and 22 mt/ha was mixed with Mountview silt loam (Typic Paleudults) limed to pH 5.8 and 7.2. Three clippings each of fescue (Festuca arundiancea Schreb.), and Swiss chard (Beta vulgaris L.), and one harvest of wheat (Triticum aestivum L.) for grain and straw were grown on separate series of treated soil, and plant samples were analyzed for radioactivity due to 226Ra uptake. Samples of sugarcane (Saccharum officinarum L.) forage and extracted juice from field experiments in Florida testing this slage as a Si source also were analyzed for radioactivity. Dry forage yields of fescue and wheat were not affected by slag applications, but those of Swiss chard were somewhat higher on slag-treated soil at pH 5.8. Wheat grain and straw yields were higher on soil at pH 7.2 than at pH 5.8 regardless of slag treatment. Uptake of 226Ra by fescue forage and wheat grain and straw was not affected by slag application. Concentrations of 226Ra were similar in forage and extracted juice from untreated sugarcane or that treated with slag at rates up to 5.6 mt/ha. These results suggest that plant uptake of radionuclides is negligible from calcium silicate slag applied at the recommended rates for liming acid soils or as a source of Si for sugarcane

  6. Luminescence properties of dysprosium doped calcium magnesium silicate phosphor by solid state reaction method

    International Nuclear Information System (INIS)

    Dysprosium doped calcium magnesium silicate (CaMgSi2O6:Dy3+) white light emitting phosphor was synthesized by solid state reaction process. The crystal structure of sintered phosphor was monoclinic structure with space group C2/c. Chemical composition of the sintered CaMgSi2O6:Dy3+ phosphor was confirmed by EDX. The prepared CaMgSi2O6:Dy3+ phosphor was excited from 352 nm and their corresponding emission spectra were recorded at blue (470 nm), yellow (570 nm) and red (675 nm) line due to the 4F9/2 → 6H15/2, 4F9/2 → 6H13/2, 4F9/2 → 6H11/2 transitions of Dy3+ ions. The combination of these three emissions constituted as white light confirmed by the Commission Internationale de L'Eclairage (CIE) chromatic coordinate diagram. The possible mechanism of the white light emitting long lasting CaMgSi2O6:Dy3+ phosphor was also investigated. Investigation on afterglow property show that phosphor held fast and slow decay process. The peak of mechanoluminescence (ML) intensity increases linearly with increasing impact velocity of the moving piston. Thus the present investigation indicates that the local piezoelectricity-induced electron bombardment model is responsible to produce ML in prepared CaMgSi2O6:Dy3+ phosphor. - Highlights: • The crystal structure of CaMgSi2O6:Dy3+ phosphor is consistent with standard monoclinic structure. • CIE coordinates of CaMgSi2O6:Dy3+ phosphor is suitable as white light emitting phosphor. • The local piezoelectricity-induced electron bombardment model is responsible to produce ML in CaMgSi2O6:Dy3+ phosphor

  7. Luminescence properties of dysprosium doped di-calcium di-aluminium silicate phosphors

    Science.gov (United States)

    Tiwari, Geetanjali; Brahme, Nameeta; Sharma, Ravi; Bisen, D. P.; Sao, Sanjay K.; Tigga, Shalinta

    2016-08-01

    A Dysprosium doped di-calcium di-aluminium silicate phosphor emitting long-lasting white light was prepared and investigated. Phosphors were synthesized by combustion-assisted method. The effect of doping concentration on the crystal structure and luminescence properties of Ca2Al2SiO7:Dy3+ phosphors were investigated. The phase structure, surface morphology, particle size, elemental analysis was analyzed by using X-ray diffraction (XRD), transmission electron microscope (TEM), Scanning electron microscopy (SEM) and Energy dispersive X-ray spectroscopy (EDX) techniques. X-ray diffraction (XRD) profiles showed that all peaks could be attributed to the tetragonal Ca2Al2SiO7 phase when the sample was annealed at 1100 °C. The increase in TL intensity indicates that the concentration of traps increases with UV irradiation. Under the UV-excitation, the Thermoluminescence (TL) emission spectra of Ca2Al2SiO7:Dy3+ phosphor shows the characteristic emission of Dy3+ peaking at 484 nm (blue), 583 nm (yellow) and 680 nm (red), originating from the transitions of 4F9/2 → 6H15/2, 4F9/2 → 6H13/2 and 4F9/2 → 6H11/2. Photoluminescence (PL) decay has also reported and it indicates that Ca2Al2SiO7:Dy3+ phosphor contains fast decay and slow decay process. The peak of Mechanoluminescence (ML) intensity increases linearly with increasing impact velocity of the moving piston. The possible mechanism of Thermoluminescence (TL), Photoluminescence (PL) and Mechanoluminescence (ML) of this white light emitting long lasting phosphor is also investigated.

  8. Effects of Surface Treatments on the Bond Strength Between Resin Cement and a New Zirconia-reinforced Lithium Silicate Ceramic.

    Science.gov (United States)

    Sato, T P; Anami, L C; Melo, R M; Valandro, L F; Bottino, M A

    2016-01-01

    This study evaluated the effects of surface treatments on the bond strength between the new zirconia-reinforced lithium silicate ceramic (ZLS) and resin cement. VITA Suprinity blocks were crystallized according to the manufacturer's instructions and randomly assigned to six groups (N=36; n=6), according to the surface treatment to be performed and aging conditions: HF20, 10% hydrofluoric acid for 20 seconds, baseline (control); HF20tc, 10% hydrofluoric acid for 20 seconds, aging; HF40, 10% hydrofluoric acid for 40 seconds, baseline; HF40tc, 10% hydrofluoric acid for 40 seconds, aging; CJ, CoJet sandblasting (25 seconds, 2.5 bar, 15-mm distance), baseline; and CJtc, CoJet sandblasting (25 seconds, 2.5 bar, 15-mm distance), aging. All specimens were silanized (Monobond S) and cemented with Panavia F to newly polymerized Z250 resin blocks. After specimens were immersed for 24 hours in distilled water at 37° C, 1-mm(2) cross-section microbars were obtained by means of a cutting machine under constant cooling. Baseline groups were immediately tested, whereas "tc" groups were used to analyze the effect of aging on bond strength (10,000 thermal cycles, 5/55°C, 30-second bath). The microtensile bond strength test was performed with a universal testing machine (0.5 mm/min), and bond strength (MPa) was calculated when the load-to-failure (N) was divided by the adhesive area (mm(2)). We also evaluated the surface roughness (Sa, average roughness; Str, texture aspect ratio; Sdr, developed interfacial area ratio) and the contact angle resulting from the treatments. Data were statistically analyzed by one- or two-way analysis of variance and Tukey's test (all α=5%). The failure mode of each specimen was evaluated by stereomicroscopy, and representative specimens were analyzed by scanning electron microscopy. The microtensile bond strength was affected by the surface conditioning (p<0.0001), storage condition (p<0.0001), and the interaction between them (p=0.0012). The

  9. Self-Setting Calcium Phosphate Cements with Tunable Antibiotic Release Rates for Advanced Antimicrobial Applications.

    Science.gov (United States)

    Ghosh, Shreya; Wu, Victoria; Pernal, Sebastian; Uskoković, Vuk

    2016-03-30

    Osteomyelitis, an infectious disease predominantly tied to poor sanitary conditions in underdeveloped regions of the world, is in need of inexpensive, easily in situ synthesizable and administrable materials for its treatment. The results of this study stem from the attempt to create one such affordable and minimally invasive therapeutic platform in the form of a self-setting, injectable cement with a tunable drug release profile, composed of only nanoparticulate hydroxyapatite, the synthetic version of the bone mineral. Cements comprised two separately synthesized hydroxyapatite powders, one of which, HAP2, was precipitated abruptly, retaining the amorphous nature longer, and the other one of which, HAP1, was precipitated at a slower rate, more rapidly transitioning to the crystalline structure. Cements were made with four different weight ratios of the two hydroxyapatite components: 100/0, 85/15, 50/50, and 0/100 with respect to HAP1 and HAP2. Both the setting and the release rates measured on two different antibiotics, vancomycin and ciprofloxacin, were controlled using the weight ratio of the two hydroxyapatite components. Various inorganic powder properties were formerly used to control drug release, but here we demonstrate for the first time that the kinetics of the mechanism of formation of a solid compound can be controlled to produce tunable drug release profiles. Specifically, it was found that the longer the precursor calcium phosphate component of the cement retains the amorphous nature of the primary precipitate, the more active it was in terms of speeding up the diffusional release of the adsorbed drug. The setting rate was, in contrast, inversely proportional to the release rate and to the content of this active hydroxyapatite component, HAP2. The empirical release profiles were fitted to a set of equations that could be used to tune the release rate to the therapeutic occasion. All of the cements loaded with vancomycin or ciprofloxacin inhibited the

  10. Understanding silicate hydration from quantitative analyses of hydrating tricalcium silicates.

    Science.gov (United States)

    Pustovgar, Elizaveta; Sangodkar, Rahul P; Andreev, Andrey S; Palacios, Marta; Chmelka, Bradley F; Flatt, Robert J; d'Espinose de Lacaillerie, Jean-Baptiste

    2016-01-01

    Silicate hydration is prevalent in natural and technological processes, such as, mineral weathering, glass alteration, zeolite syntheses and cement hydration. Tricalcium silicate (Ca3SiO5), the main constituent of Portland cement, is amongst the most reactive silicates in water. Despite its widespread industrial use, the reaction of Ca3SiO5 with water to form calcium-silicate-hydrates (C-S-H) still hosts many open questions. Here, we show that solid-state nuclear magnetic resonance measurements of (29)Si-enriched triclinic Ca3SiO5 enable the quantitative monitoring of the hydration process in terms of transient local molecular composition, extent of silicate hydration and polymerization. This provides insights on the relative influence of surface hydroxylation and hydrate precipitation on the hydration rate. When the rate drops, the amount of hydroxylated Ca3SiO5 decreases, thus demonstrating the partial passivation of the surface during the deceleration stage. Moreover, the relative quantities of monomers, dimers, pentamers and octamers in the C-S-H structure are measured. PMID:27009966

  11. Understanding silicate hydration from quantitative analyses of hydrating tricalcium silicates

    Science.gov (United States)

    Pustovgar, Elizaveta; Sangodkar, Rahul P.; Andreev, Andrey S.; Palacios, Marta; Chmelka, Bradley F.; Flatt, Robert J.; D'Espinose de Lacaillerie, Jean-Baptiste

    2016-03-01

    Silicate hydration is prevalent in natural and technological processes, such as, mineral weathering, glass alteration, zeolite syntheses and cement hydration. Tricalcium silicate (Ca3SiO5), the main constituent of Portland cement, is amongst the most reactive silicates in water. Despite its widespread industrial use, the reaction of Ca3SiO5 with water to form calcium-silicate-hydrates (C-S-H) still hosts many open questions. Here, we show that solid-state nuclear magnetic resonance measurements of 29Si-enriched triclinic Ca3SiO5 enable the quantitative monitoring of the hydration process in terms of transient local molecular composition, extent of silicate hydration and polymerization. This provides insights on the relative influence of surface hydroxylation and hydrate precipitation on the hydration rate. When the rate drops, the amount of hydroxylated Ca3SiO5 decreases, thus demonstrating the partial passivation of the surface during the deceleration stage. Moreover, the relative quantities of monomers, dimers, pentamers and octamers in the C-S-H structure are measured.

  12. Improvement of bioactivity, degradability, and cytocompatibility of biocement by addition of mesoporous magnesium silicate into sodium-magnesium phosphate cement.

    Science.gov (United States)

    Wu, Yingyang; Tang, Xiaofeng; Chen, Jie; Tang, Tingting; Guo, Han; Tang, Songchao; Zhao, Liming; Ma, Xuhui; Hong, Hua; Wei, Jie

    2015-09-01

    A novel mesoporous magnesium-based cement (MBC) was fabricated by using the mixed powders of magnesium oxide, sodium dihydrogen phosphate, and mesoporous magnesium silicate (m-MS). The results indicate that the setting time and water absorption of the MBC increased as a function of increasing m-MS content, while compressive strength decreased. In addition, the degradability of the MBC in a solution of Tris-HCl and the ability of apatite formation on the MBC were significantly improved with the increase in m-MS content. In cell culture experiments, the results show that the attachment, proliferation, and alkaline phosphatase activity of the MC3T3-E1 cells on the MBC were significantly enhanced with the increase of the content of m-MS. It can be suggested that the MBC with good cytocompatibility could promote the proliferation and differentiation of the MC3T3-E1 cells. In short, our findings indicate that the MBC containing m-MS had promising potential as a new biocement for bone regeneration and repair applications. PMID:26395363

  13. A new acoustic method to determine the setting time of calcium sulfate bone cement mixed with antibiotics

    International Nuclear Information System (INIS)

    A new method is described which can be used to determine the setting times of small amounts of high value bone cements. The test was developed to measure how the setting times of a commercially available synthetic calcium sulfate cement (Stimulan, Biocomposites, UK) in two forms (standard and Rapid Cure) varies with the addition of clinically relevant antibiotics. The importance of being able to accurately quantify these setting times is discussed. The results demonstrate that this new method, which is shown to correlate to the Vicat needle, gives reliable and repeatable data with additional benefits expressed in the article. The majority of antibiotics mixed were found to retard the setting reaction of the calcium sulfate cement. (paper)

  14. Calcium phosphate cements properties with polymers addition; Propriedades do cimento de fosfato de calcio com adicao de polimeros

    Energy Technology Data Exchange (ETDEWEB)

    Fernandes, J.M.; Trajano, W.T.; Escobar, C.F.; Santos, L.A., E-mail: julianafernandes2@yahoo.com.br [Universidade Federal do Rio Grande do Sul (UFRGS), RS (Brazil)

    2012-07-01

    Calcium phosphate cements (CPC) have attracted great interest to use in orthopedics and dentistry as replacements for damaged parts of the skeletal system, showing good biocompatibility and osseointegration, allowing its use as bone graft. Several studies have shown that the addition of polymer additives have a strong influence on the cement properties. The low mechanical strength is the main obstacle to greater use of CPC as an implant material. The objective of this study was to evaluate properties of a cement based on α-tricalcium phosphate (α-TCP), added polymers. PVA (10%, 8%, 6%), sodium alginate (2%) and polyacrylate ammonia (3%), all in weight, were added to the synthesized α-TCP powder. The samples were molded and evaluated for density, porosity in vitro test (Simulated Body Fluid), crystalline phases and mechanical strength. The results show increased the mechanical properties of the cement when added these polymers.

  15. Cytotoxic effects of mineral trioxide aggregate, calcium enrichedmixture cement, Biodentine and octacalcium pohosphate onhuman gingival fibroblasts

    Science.gov (United States)

    A. Saberi, Eshagh; Farhadmollashahi, Narges; Ghotbi, Faroogh; Karkeabadi, Hamed; Havaei, Roholla

    2016-01-01

    Background. This in vitro study compared the effects of mineral trioxide aggregate (MTA), calcium enriched mixture(CEM) cement, Biodentine (BD) and octacalcium phosphate (OCP) on the viability of human gingival fibroblasts (HGFs). Methods. After completion of the setting time of the materials under study, fibroblasts were placed in 24-well insert platesand 1 mg of each material was added to the respective wells. The plates were then incubated at 37°C. The inserts were removedat 24, 48 and 168 hours and 2,5-diphenyltetrazolium bromide was added to assess cytotoxicity via the MTT colorimetricassay. Data were analyzed at different time intervals using repeated-measures ANOVA, followed by the Bonferronitest at three levels of significance of P MTA (P MTA, CEM, Biodentine and OCP against HGFs was similar to that of the control group at 24and 48 hours. Over time, MTA and Biodentine exhibited less cytotoxicity than other materials. PMID:27429722

  16. Corrosion resistance of enamel coating modified by calcium silicate and sand particle for steel reinforcement in concrete

    Science.gov (United States)

    Tang, Fujian

    Porcelain enamel has stable chemical property in harsh environments such as high temperature, acid and alkaline, and it can also chemically react with substrate reinforcing steel resulting in improved adherence strength. In this study, the corrosion resistances of enamel coating modified by calcium silicate and sand particles, which are designed for improved bond strength with surrounding concrete, were investigated in 3.5 wt% NaCl solution. It consists of two papers that describe the results of the study. The first paper investigates the corrosion behavior of enamel coating modified by calcium silicate applied to reinforcing steel bar in 3.5 wt% NaCl solution by OCP, electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization. The coatings include a pure enamel, a mixed enamel that consists of 50% pure enamel and 50% calcium silicate by weight, and a double enamel that has an inner pure enamel layer and an outer mixed enamel layer. Electrochemical tests demonstrates that both pure and double enamel coatings can significantly improve corrosion resistance, while the mixed enamel coating offers very little protection due to connected channels. The second paper is focused on the electrochemical characteristics of enamel coating modified by sand particle applied to reinforcing steel bar in 3.5 wt% NaCl solution by EIS. Six percentages by weight are considered including 5%, 10%, 20%, 30%, 50%, and 70%. Results reveal that addition of sand particle does not affect its corrosion resistance significantly. Most of the sand particles can wet very well with enamel body, while some have a weak zone which is induced during the cooling stage due to different coefficient of thermal expansion. Therefore, quality control of sand particle is the key factor to improve its corrosion resistance.

  17. Effects of adding resorbable chitosan microspheres to calcium phosphate cements for bone regeneration

    Energy Technology Data Exchange (ETDEWEB)

    Meng, Dan [Department of Prosthodontics, Beijing Stomatological Hospital, Capital Medical University, Beijing 100050 (China); Dong, Limin [Beijing Key Lab of Fine Ceramics, Institute of Nuclear and New Energy Technology, Tsinghua University, Energy Science Building, Beijing 100084 (China); Wen, Ying [Department of Prosthodontics, Beijing Stomatological Hospital, Capital Medical University, Beijing 100050 (China); Xie, Qiufei, E-mail: xieqiuf@163.com [Department of Prosthodontics, Peking University School and Hospital of Stomatology, Beijing 100081 (China)

    2015-02-01

    Calcium phosphate cements (CPCs) have been widely used as bone graft substitutes. However, the undesirable osteoinductivity and slow degradability of CPCs greatly hamper their clinical application. The aim of this study was to synthesize a type of injectable, bioactive cement. This was accomplished by incorporating chitosan microspheres into CPC. CPC containing chitosan microspheres was analyzed by X-ray diffraction (XRD) and scanning electron microscope (SEM). XRD showed that the hardened chitosan microsphere/CPC with different proportions of microspheres contained diffraction peaks of hydroxyapatite and chitosan. Compressive strength and dissolution in simulated body fluid were measured. The chitosan microsphere/CPC containing 10% (w/w) chitosan microspheres had a compressive strength of 14.78 ± 0.67 MPa. Cavity defects were created in both femoral condylar regions of New Zealand White rabbits. Chitosan microsphere/CPC (composite group) and α-TCP/CPC (control group) were implanted separately into the bone defects of both femurs. X-ray analysis was performed to observe the filling of these bone defects 3 days after surgery. The extent of bone substitute degradation and new bone formation were evaluated by SEM and histological examination at 8, 16, and 24 weeks after implantation. These results showed far more new bone formation and degradation of the chitosan microsphere/CPC composite in the bone defects. These data indicate that a chitosan microsphere/CPC composite might be considered as a promising injectable material for the generation of new bone tissue. - Highlights: • We synthesized an injectable, bioactive chitosan microsphere/CPC for the first time. • 100–400 μm chitosan microspheres were incorporated into the cement solid phase. • XRD showed the construct contained diffraction peaks of hydroxyapatite and chitosan. • Compressive strength of the composite was about 15 MPa comparable to cancellous bone. • The new construct shows better bone

  18. Effects of adding resorbable chitosan microspheres to calcium phosphate cements for bone regeneration

    International Nuclear Information System (INIS)

    Calcium phosphate cements (CPCs) have been widely used as bone graft substitutes. However, the undesirable osteoinductivity and slow degradability of CPCs greatly hamper their clinical application. The aim of this study was to synthesize a type of injectable, bioactive cement. This was accomplished by incorporating chitosan microspheres into CPC. CPC containing chitosan microspheres was analyzed by X-ray diffraction (XRD) and scanning electron microscope (SEM). XRD showed that the hardened chitosan microsphere/CPC with different proportions of microspheres contained diffraction peaks of hydroxyapatite and chitosan. Compressive strength and dissolution in simulated body fluid were measured. The chitosan microsphere/CPC containing 10% (w/w) chitosan microspheres had a compressive strength of 14.78 ± 0.67 MPa. Cavity defects were created in both femoral condylar regions of New Zealand White rabbits. Chitosan microsphere/CPC (composite group) and α-TCP/CPC (control group) were implanted separately into the bone defects of both femurs. X-ray analysis was performed to observe the filling of these bone defects 3 days after surgery. The extent of bone substitute degradation and new bone formation were evaluated by SEM and histological examination at 8, 16, and 24 weeks after implantation. These results showed far more new bone formation and degradation of the chitosan microsphere/CPC composite in the bone defects. These data indicate that a chitosan microsphere/CPC composite might be considered as a promising injectable material for the generation of new bone tissue. - Highlights: • We synthesized an injectable, bioactive chitosan microsphere/CPC for the first time. • 100–400 μm chitosan microspheres were incorporated into the cement solid phase. • XRD showed the construct contained diffraction peaks of hydroxyapatite and chitosan. • Compressive strength of the composite was about 15 MPa comparable to cancellous bone. • The new construct shows better bone

  19. Indirect pulp therapy in a symptomatic mature molar using calcium enriched mixture cement

    Directory of Open Access Journals (Sweden)

    Hassan Torabzadeh

    2013-01-01

    Full Text Available Dental pulp has the ability of repair/regeneration. Indirect pulp therapy (IPT is recommended for pulp preservation in asymptomatic teeth with extremely deep caries as well as teeth with clinical symptoms of reversible pulpitis. In this case study, we performed IPT with calcium enriched mixture (CEM cement on a symptomatic permanent molar. After clinical/radiographic examinations the tooth was diagnosed with irreversible pulpitis and associated apical periodontitis. IPT involved partial caries removal, the placement of CEM cement pulp cap and overlying adhesive permanent restoration. At the 1 week follow-up, patient′s spontaneous symptoms had resolved. One-year follow-up demonstrated pulp vitality, clinical function, as well as the absence of pain/tenderness to percussion/palpation/cold sensitivity tests; periapical radiograph showed a healing periradicular lesion with newly formed bone, that is normal pulp with normal periodontium. These favorable results indicate that IPT/CEM may be a good treatment option in comparison to endodontic treatment in young patients. IPT of deep-caries lesion is an easier, more practical and valuable treatment plan than complete caries removal.

  20. Properties of MSW fly ash-calcium sulfoaluminate cement matrix and stabilization/solidification on heavy metals.

    Science.gov (United States)

    Qian, G R; Shi, J; Cao, Y L; Xu, Y F; Chui, P C

    2008-03-21

    In this paper, investigations were undertaken to formulate the properties of fly ash-calcium sulfoaluminate (CSA) cement matrix by blending MSW fly ash with CSA cement. The compressive strength, pore structure, hydration phases, and leaching behavior of Zn and Pb doped MSW fly ash-CSA cement matrices were determined by XRD, MIP, DSC, FTIR, EDX, TCLP leaching test and other experiments. The results showed that the addition of MSW fly ash to form fly ash-CSA cement matrix reduced the compressive strengths of matrices and made the pore distribution of matrices coarser, compared to that of pure CSA cement matrix. However, fly ash-CSA cement matrix could effectively immobilize high concentration of heavy metal such as lead and zinc with much lesser leaching of TCLP. Besides ettringite AFt, Friedel phase was a new hydration phase formed in the matrix. The formation of these hydration phases was responsible for huge reservoir of heavy metal stabilization by chemical fixing. Therefore, it could be postulated that MSW fly ash-CSA cement matrix was a potential new constituent of S/S matrix for high concentration of heavy metals such as Zn and Pb ions. PMID:17728061

  1. Luminescence properties of dysprosium doped calcium magnesium silicate phosphor by solid state reaction method

    Energy Technology Data Exchange (ETDEWEB)

    Sahu, Ishwar Prasad, E-mail: ishwarprasad1986@gmail.com [School of Studies in Physics & Astrophysics, Pt. Ravishankar Shukla University, Raipur, C.G. 492010 (India); Chandrakar, Priya; Baghel, R.N.; Bisen, D.P.; Brahme, Nameeta [School of Studies in Physics & Astrophysics, Pt. Ravishankar Shukla University, Raipur, C.G. 492010 (India); Tamrakar, Raunak Kumar [Department of Applied Physics, Bhilai Institute of Technology, Durg, C.G. 491001 (India)

    2015-11-15

    Dysprosium doped calcium magnesium silicate (CaMgSi{sub 2}O{sub 6}:Dy{sup 3+}) white light emitting phosphor was synthesized by solid state reaction process. The crystal structure of sintered phosphor was monoclinic structure with space group C2/c. Chemical composition of the sintered CaMgSi{sub 2}O{sub 6}:Dy{sup 3+} phosphor was confirmed by EDX. The prepared CaMgSi{sub 2}O{sub 6}:Dy{sup 3+} phosphor was excited from 352 nm and their corresponding emission spectra were recorded at blue (470 nm), yellow (570 nm) and red (675 nm) line due to the {sup 4}F{sub 9/2} → {sup 6}H{sub 15/2}, {sup 4}F{sub 9/2} → {sup 6}H{sub 13/2}, {sup 4}F{sub 9/2} → {sup 6}H{sub 11/2} transitions of Dy{sup 3+} ions. The combination of these three emissions constituted as white light confirmed by the Commission Internationale de L'Eclairage (CIE) chromatic coordinate diagram. The possible mechanism of the white light emitting long lasting CaMgSi{sub 2}O{sub 6}:Dy{sup 3+} phosphor was also investigated. Investigation on afterglow property show that phosphor held fast and slow decay process. The peak of mechanoluminescence (ML) intensity increases linearly with increasing impact velocity of the moving piston. Thus the present investigation indicates that the local piezoelectricity-induced electron bombardment model is responsible to produce ML in prepared CaMgSi{sub 2}O{sub 6}:Dy{sup 3+} phosphor. - Highlights: • The crystal structure of CaMgSi{sub 2}O{sub 6}:Dy{sup 3+} phosphor is consistent with standard monoclinic structure. • CIE coordinates of CaMgSi{sub 2}O{sub 6}:Dy{sup 3+} phosphor is suitable as white light emitting phosphor. • The local piezoelectricity-induced electron bombardment model is responsible to produce ML in CaMgSi{sub 2}O{sub 6}:Dy{sup 3+} phosphor.

  2. Characterization of cement pastes by inverse gas chromatography

    OpenAIRE

    BENZARTI, K; V. Oliva; CHEHIMI, MM; BAETA NEVES, MI

    2002-01-01

    Two cement pastes, commonly used in concrete formulations, were characterized by IGC at 35-80°C before and after coating with an epoxy resin and a hardener. The cements are mixtures of hydrates in various proportions, such as calcium silicate hydrate (CaO-SiO2-H2O) and calcium hydroxyde Ca(OH)2. Apolar and polar probes were used to determine the cements dispersive and acid-base characteristics. The materials appear as high surface energy materials as judged from the dispersive contribution to...

  3. Effect of citric acid and the hemihydrate amount on the properties of a calcium sulphoaluminate cement

    Directory of Open Access Journals (Sweden)

    Velazco, G.

    2014-12-01

    Full Text Available The influence of citric acid on the hydration and strength development of a calcium sulphoaluminate cement was investigated. Cement pastes were prepared by mixing calcium sulphoaluminate (C4A3Ŝ with 15, 20 and 25wt% of hemihydrate (CŜH0.5. Citric acid was added as a retarder at 0 and 0.5wt%. The samples were cured at 20 °C for periods of time from 1 to 28 days to evaluate their compressive strength and to characterize the hydration products by scanning electron microscopy and X-ray diffraction. Calorimetric curves showed that the retarding agent considerably decreases the heat release rate and the quantity of total heat released. The main product after the curing was ettringite (C6AŜ3H32. The morphology of this phase consisted of long and thin needles growing radially on the cement grains. Samples with 15wt% of hemihydrate and 0.5wt% of citric acid developed the highest compressive strength (70 MPa at 28 days of curing.Se investigó el efecto del ácido cítrico sobre la hidratación y propiedades mecánicas de un cemento de sulfoaluminato de calcio. El C4A3Ŝ se mezcló con 15, 20 y 25% e.p. de hemihidrato (CŜH0.5. Se agregó ácido cítrico como retardante en 0 y 0.5% e.p. Las muestras fueron curadas a 20 °C por periodos de 1 a 28 días para realizar mediciones de resistencia a la compresión y caracterizar los productos de hidratación mediante microscopía electrónica de barrido y difracción de rayos X. Las curvas de calorimetría mostraron ue el ácido cítrico disminuye la velocidad de liberación de calor y la cantidad de calor liberado durante la hidratación. La resistencia a la compresión alcanzó un máximo de 70 MPa en muestras con 15% e.p. de hemihidrato y 0,5% e.p de ácido cítrico. Los resultados muestran a la etringita (C6AŜ3H32 como principal producto de hidratación. Se observa a esta fase con morfología acicular creciendo sobre las partículas de cemento.

  4. Wollastonite nanofiber–doped self-setting calcium phosphate bioactive cement for bone tissue regeneration

    Directory of Open Access Journals (Sweden)

    Guo H

    2012-07-01

    Full Text Available Han Guo,1,2 Jie Wei,2 Wenhua Song,2 Shan Zhang,2 Yonggang Yan,3 Changsheng Liu,2 Tiqiao Xiao11Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai, People's Republic of China; 2Key Laboratory for Ultrafine Materials of Ministry of Education, East China University of Science and Technology, Shanghai, People's Republic of China; 3School of Physical Science and Technology, Sichuan University, Chengdu, People's Republic of ChinaAbstract: The purpose of this study was to synthesize a self-setting bioactive cement by incorporation of wollastonite nanofibers (WNFs into calcium phosphate cement (CPC. The composition, morphology, setting time, compressive strength, hydrophilicity, and degradation of WNF-doped CPC (wnf-CPC were investigated. Scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, and inductively coupled plasma atomic emission spectroscopy were utilized. Additionally, methyl-thiazolyl-tetrazolium bromide assay, scanning electron microscopy, inductively coupled plasma atomic emission spectroscopy, and histological evaluation were used to study the cell and tissue responses to wnf-CPC, both in vitro and in vivo. The results confirmed that the addition of WNFs into CPC had no obvious effect on the setting time or the compressive strength of wnf-CPC, provided the WNF amount was not more than 10 wt%. However, the hydrophilicity and degradability of wnf-CPC were significantly improved by the addition of WNFs – this was because of the change of microstructure caused by the WNFs. The preferred dissolution of WNFs caused the formation of microporosity in wnf-CPC when soaked in tris hydrochloride solution. The microporosity enlarged the surface area of the wnf-CPC and so promoted degradation of the wnf-CPC when in contact with liquid. In addition, MG-63 cell attachment and proliferation on the wnf-CPC were superior to that on the CPC, indicating that

  5. Porous calcium phosphate-poly (lactic-co-glycolic) acid composite bone cement: A viable tunable drug delivery system.

    Science.gov (United States)

    Roy, Abhijit; Jhunjhunwala, Siddharth; Bayer, Emily; Fedorchak, Morgan; Little, Steve R; Kumta, Prashant N

    2016-02-01

    Calcium phosphate based cements (CPCs) are frequently used as bone void fillers for non-load bearing segmental bone defects due to their clinically relevant handling characteristics and ability to promote natural bone growth. Macroporous CPC scaffolds with interconnected pores are preferred for their ability to degrade faster and enable accelerated bone regeneration. Herein, a composite CPC scaffold is developed using newly developed resorbable calcium phosphate cement (ReCaPP) formulation containing degradable microspheres of bio-compatible poly (lactic-co-glycolic acid) (PLGA) serving as porogen. The present study is aimed at characterizing the effect of in-vitro degradation of PLGA microspheres on the physical, chemical and structural characteristics of the composite cements. The porosity measurements results reveal the formation of highly interconnected macroporous scaffolds after degradation of PLGA microspheres. The in-vitro characterizations also suggest that the degradation by products of PLGA reduces the pH of the local environment thereby increasing the dissolution rate of the cement. In addition, the in-vitro vancomycin release from the composite CPC scaffold suggests that the drug association with the composite scaffolds can be tuned to achieve control release kinetics. Further, the study demonstrates control release lasting for longer than 10weeks from the composite cements in which vancomycin is encapsulated in PLGA microspheres. PMID:26652353

  6. Synthesis and mechanical properties of a calcium sulphoaluminate cement made of industrial wastes

    Directory of Open Access Journals (Sweden)

    Gallardo, M.

    2014-09-01

    Full Text Available Environmentally-friendly calcium sulphoaluminate clinkers were obtained from a mixture of aluminium dross, fluorgypsum, fly ash and CaCO₃ at temperatures within the range of 1100 to 1400 °C. After the heat treatments Ca₄Al₆O₁₂SO₄ was the main phase. Three different cements were prepared using the clinkers synthesized at 1250, 1350 and 1400 °C; the clinker powders were mixed with 20 wt% of hemihydrate. Cement pastes were prepared using a water/cement ratio (w/c, 0.4 followed by curing at 20 or 40 °C for periods of time ranging from 1 to 28 days. Most of the samples showed high compression strengths 40–47 MPa after 28 days, which were comparable to the strength of Portland cement. Ettringite was the main hydration product and its morphology consisted of acicular and hexagonal plates, which is typical of this phase.Se fabricaron clinkers de bajo impacto ambiental a base de sulfoaluminato de calcio calcinando mezclas de escoria de aluminio, fluoryeso, ceniza volante y CaCO₃ a diferentes temperaturas dentro de un rango de 1100 a 1400 °C. Se observó la formación de Ca₄Al₆O₁₂SO₄ como fase principal. Para obtener los cementos, los clinkers obtenidos a 1250, 1350 y 1400 °C se mezclaron con 20% en peso de hemihidrato. Se prepararon pastas usando una relación agua/cemento, de 0.4 y se curaron a 20 y 40 °C por diferentes periodos de tiempo desde 1 hasta 28 días. Los valores de resistencia a la compresión a los 28 días de curado de la mayoría de las muestras estuvieron entre 40–47 MPa, equiparables a los de referencia de pastas de cemento Portland. La etringita fue el principal producto de hidratación y su morfología consistió de placas hexagonales y aciculares, típicas de esta fase.

  7. Glass Polyalkenoate Cements Designed for Cranioplasty Applications: An Evaluation of Their Physical and Mechanical Properties

    OpenAIRE

    Basel A. Khader; Declan J. Curran; Sean Peel; Mark R. Towler

    2016-01-01

    Glass polyalkenoate cements (GPCs) have potential for skeletal cementation. Unfortunately, commercial GPCs all contain, and subsequently release, aluminum ions, which have been implicated in degenerative brain disease. The purpose of this research was to create a series of aluminum-free GPCs constructed from silicate (SiO2), calcium (CaO), zinc (ZnO) and sodium (Na2O)-containing glasses mixed with poly-acrylic acid (PAA) and to evaluate the potential of these cements for cranioplasty applicat...

  8. An inferred relationship between some uranium deposits and calcium carbonate cement in southern Black Hills, South Dakota

    Science.gov (United States)

    Gott, Garland B.

    1956-01-01

    Evidence resulting from geologic mapping in the southern Black Hills indicates that the areas marginal to some of the larger carbonate-cemented sandstones constitute favorable geochemical environments for the localization of uranium deposits. To determine whether these favorable environments are predictable a limited experimental core-drilling program was carried out. An extensive deposit was discovered in an area marginal to a sandstone well-cemented with calcium carbonate. The deposit has not yet been developed, but from the available data it appears that there is a significant quantity of mineralized rock present containing as much as 3.0 percent eU3O8.

  9. Preparation and rebinding properties of protein-imprinted polysiloxane using mesoporous calcium silicate grafted non-woven polypropylene as matrix.

    Science.gov (United States)

    Kan, Bohong; Feng, Lingzhi; Zhao, Kongyin; Wei, Junfu; Zhu, Dunwan; Zhang, Linhua; Ren, Qian

    2016-03-01

    Calcium silicate particle containing mesoporous SiO2 (CaSiO3@SiO2) was grafted on the surface of non-woven polypropylene. The PP non-woven grafted calcium silicate containing mesoporous SiO2 (PP-g-CaSiO3@SiO2) was used as the matrix to prepare bovine serum albumin (BSA) molecularly imprinted polysiloxane (MIP) by using silanes as the functional monomers and BSA as the template. PP non-woven grafted BSA-imprinted polysiloxane (PP-g-CaSiO3@SiO2 MIP) was characterized by scanning electron microscope (SEM), Fourier transform infrared spectometry (FTIR) and drilling string compensator (DSC). Influence factors on the rebinding capacity of the MIP were investigated, such as grafting degree, the pH in treating CaSiO3 and the type and proportion of silanes. The rebinding properties of BSA on PP-g-CaSiO3@SiO2 and MIP were investigated under different conditions. The results indicated that the rebinding capacity of MIP for BSA reached 56.32 mg/g, which was 2.65 times of NIP. The non-woven polypropylene grafted BSA-imprinted polysiloxane could recognize the template protein and the selectivity factor (β) was above 2.4 when using ovalbumin, hemoglobin and γ-globulin as control proteins. The PP-g-CaSiO3@SiO2 MIP has favorable reusability. PMID:25726930

  10. Effect of Additives on the Morphology of the Hydrated Product and Physical Properties of a Calcium Phosphate Cement

    Institute of Scientific and Technical Information of China (English)

    Xiupeng WANG; Jiandong YE; Yingjun WANG

    2008-01-01

    The morphology of a hydrated calcium phosphate cement (CPC) doped with several normally used additives was investigated by scanning electron microscopy (SEM) and the compressive strength of the cement was determined in this study. The hydrated products of CPC without additives was rod-like hydroxyapatite (HA) grains with around 2-5 μm in length and 100 nm in width. The addition of Sr obviously decreased the crystal size of the rod-like grains. CPCs containing carbonate, collagen and gelatin showed flake-like crystal morphology. Crylic acid-containing CPC presented flocculus-like structure. And malic acid-containing CPC exhibited oriented flake-like structure. The X-ray diffraction (XRD) analysis showed that the additives used in this study did not alter the hydration products of the cement. The compressive strength tests indicated that the compressive strength of the cement with rod-like morphology HA crystals was much higher than that of the cement with flake-like morphology HA crystals, and the cement with oriented flake-like morphology HA crystals .exhibited the poorest compressive strength.

  11. Comparative study on the change in index of refraction in ion-exchange interdiffusion in alkali-silicate glasses containing calcium, strontium, barium and titanium oxides

    International Nuclear Information System (INIS)

    Different ability to ion exchange from the salts of lithium-sodium-silicate glass melt containing calcium (or strontium, or barium) and titanium oxides in addition has been shown. CaO, SrO and BaO have negative effect, but TiO2 -positive one on the fullness of ion exchange of lithium-sodium and on the rate of interdiffusion in alkali-silicate glass. The value of change in index of refraction of glass with TiO2 is twice higher than glass with calcium oxide (or strontium, or barium) as the fourth component

  12. Preparation and Characterization of Ni-Doped Calcium Silicate Hydrate Based on Steel Slag: Adsorption Capacity for Rhodamine B from Aqueous Solution

    OpenAIRE

    2015-01-01

    Calcium silicate hydrate based on steel slag (SCSH) and Ni-doped SCSH (NSCSH) were synthesized under specific hydrothermal conditions at saturated vapor pressure and 185°C for 7 hours. The structure and morphology of SCSH and NSCSH were characterized by XRD, SEM, and N2 adsorption/desorption. SCSH mainly consisted of amorphous calcium silicate hydrate gel (C-S-H gel) together with some flake-like tobermorite and NSCSH consisted of crystalline tobermorite and xonotlite. The addition of Ni(NO3)...

  13. Beneficial use of a cell coupling rheometry, conductimetry, and calorimetry to investigate the early age hydration of calcium sulfo-aluminate cement

    International Nuclear Information System (INIS)

    A specific cell was designed to monitor simultaneously the evolution of the viscoelastic properties, electrical conductivity, and temperature of a cement paste with ongoing hydration. Hydration of calcium sulfo-aluminate cement by demineralized water or by a borated solution was then investigated as an example. Borate anions acted as set retarders but to a smaller extent than with ordinary Portland cement. The delay in cement hydration resulted from the precipitation of an amorphous or poorly crystallized calcium borate, which also caused a rapid stiffening (and thus a loss of workability) of the paste after mixing. The gypsum content of the CSA cement was shown to play a key role in the control of the cement reactivity. (authors)

  14. Notes on hydrated cement fractals investigated by SANS

    Energy Technology Data Exchange (ETDEWEB)

    Ficker, T [Faculty of Civil Engineering, Physics Department, Technical University, Zizkova 17, CZ-602 00 Brno (Czech Republic); Len, A [Budapest Neutron Centre, Konkoly Thege 29-33, H-1525 Budapest (Hungary); Nemec, P [Faculty of Civil Engineering, Physics Department, Technical University, Zizkova 17, CZ-602 00 Brno (Czech Republic)

    2007-07-07

    Hydrated cement pastes with different water-to-cement ratios have been investigated by the small-angle scattering neutron technique. Special attention has been paid to the fractal nanostructure of the calcium silicate hydrate (C-S-H solid gel) and its basic building particles, i.e. nanometric globules. The inner stability of these particles has been tested and shown to be sufficiently persistent to withstand all spatial regroupings of the overall nanostructure caused by variations of w/c ratios.

  15. Early age corrosion of aluminium in calcium sulfo-aluminate cement based composites

    International Nuclear Information System (INIS)

    At present, encapsulation of low level and intermediate level nuclear wastes using Portland Cement (PC) based matrices is a preferred approach. However, it is now widely accepted that the high pH of the pore solution of these PC-based matrices (usually above pH 12.5) can cause concerns over the stability of certain wastes containing reactive metals, such as aluminium and uranium. One potential low pH system for reducing the corrosion of aluminium is calcium sulfo-aluminate cement (CSA). However, significant heat could be generated from the hydration of CSA, causing another concern to the nuclear industry. In the current study, various additives, namely pulverized fuel ash (PFA), ground granulated blast furnace slag (GGBS) and limestone powder (LSP) were used to replace part of the CSA in order to reduce the heat output. The results indicated that the replacement of CSA with GGBS, PFA and LSP can reduce the heat output of 100% CSA, although it is still higher than the control GGBS/PC 9:1 system. The corrosion rate of aluminium in each of the CSA composites was slightly higher than 100% CSA, however, all the CSA systems had corrosion rates lower than GGBS/PC 9:1 after 15 hours. Therefore, the composite CSA systems investigated in this study provide a good compromise between the heat output and the resistance to the corrosion of aluminium. Hence, offers a good potential for dealing with some historical nuclear wastes where the corrosion of aluminium is a concern. (authors)

  16. Evaluation of colloidal silica suspension as efficient additive for improving physicochemical and in vitro biological properties of calcium sulfate-based nanocomposite bone cement.

    Science.gov (United States)

    Borhan, Shokoufeh; Hesaraki, Saeed; Ahmadzadeh-Asl, Shaghayegh

    2010-12-01

    In the present study new calcium sulfate-based nanocomposite bone cement with improved physicochemical and biological properties was developed. The powder component of the cement consists of 60 wt% α-calcium sulfate hemihydrate and 40 wt% biomimetically synthesized apatite, while the liquid component consists of an aqueous colloidal silica suspension (20 wt%). In this study, the above mentioned powder phase was mixed with distilled water to prepare a calcium sulfate/nanoapatite composite without any additive. Structural properties, setting time, compressive strength, in vitro bioactivity and cellular properties of the cements were investigated by appropriate techniques. From X-ray diffractometer analysis, except gypsum and apatite, no further phases were found in both silica-containing and silica-free cements. The results showed that both setting time and compressive strength of the calcium sulfate/nanoapatite cement improved by using colloidal silica suspension as cement liquid. Meanwhile, the condensed phase produced from the polymerization process of colloidal silica filled the micropores of the microstructure and covered rodlike gypsum crystals and thus controlled cement disintegration in simulated body fluid. Additionally, formation of apatite layer was favored on the surfaces of the new cement while no apatite precipitation was observed for the cement prepared by distilled water. In this study, it was also revealed that the number of viable osteosarcoma cells cultured with extracts of both cements were comparable, while silica-containing cement increased alkaline phosphatase activity of the cells. These results suggest that the developed cement may be a suitable bone filling material after well passing of the corresponding in vivo tests. PMID:20972610

  17. Preparation and characterization of a novel strontium-containing calcium phosphate cement with the two-step hydration process.

    Science.gov (United States)

    Yu, Tao; Ye, Jiandong; Wang, Yingjun

    2009-09-01

    A novel Sr-containing calcium phosphate cement (CPC) with excellent compressive strength, good radiopacity and suitable setting time was developed in this work. The two-step hydration reaction resulted in a high compressive strength, with a maximum of up to 74.9MPa. Sr was doped into the calcium-deficient hydroxyapatite as a hydrated product during the hydration reaction of the CPC. Because of the existence of Sr element and the compact microstructure after hydration, the Sr-containing CPC shows good radiopacity. It is expected to be used in orthopedic and maxillofacial surgery for bone defects repairing. PMID:19380262

  18. In vitro surface reaction layer formation and dissolution of calcium phosphate cement-bioactive glass composites

    Energy Technology Data Exchange (ETDEWEB)

    Liu Changsheng [Key Laboratory for Ultrafine Materials of Ministry of Education, and Engineering Research Center for Biomedical Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237 (China); Chen, C.-W.; Ducheyne, Paul [Center for Bioactive Materials and Tissue Engineering, Department of Bioengineering, University of Pennsylvania, Philadelphia, PA 19104 (United States)], E-mail: liucs@ecust.edu.cn, E-mail: ducheyne@seas.upenn.edu

    2008-09-01

    Composites of hydrated calcium phosphate cement (CPC) and bioactive glass (BG) containing Si were immersed in vitro to study the effect of chemical composition on surface reaction layer formation and dissolution/precipitation behavior. The solutions used were 0.05 M tris hydroxymethyl aminomethane/HCl (tris buffer), tris buffer supplemented with plasma electrolyte (TE) with pH 7.4 at 37 deg. C, and this solution complemented with 10% newborn bovine serum (TES). The post-immersion solutions were analyzed for changes in Ca, PO{sub 4} and Si concentrations. The reacted surfaces were analyzed using Fourier transform infrared (FTIR), and scanning electron microscopy with energy dispersive x-ray analysis. The sample weight variations after immersion were also determined. The results showed that the composition of the bioactive composite CPCs greatly affected their behavior in solution and the formation of apatite bioactive surface reaction layers. After immersion in the TE solution, Ca ions were taken up by all samples during the entire immersion duration. Initially, the P ion concentration increased sharply, and then decreased. This reaction pattern reveals the formation of an amorphous calcium phosphate layer on the surface of these composite CPCs. FTIR revealed that the layer was, in fact, poorly crystallized Ca-deficient carbonate apatite. The thickness of the layer was 12-14 {mu}m and it was composed of rod-like apatite with directional arrangement. For immersion in the TES solution, the Ca and Si ion concentrations showed a similar behavior to that in TE, but the release rate of Si ions was higher. FTIR revealed that after TES immersion, not only did the typical, poorly crystallized, Ca-deficient carbonated apatite form, as it did in TE, but also the serum proteins co-adsorbed on the surface and thereby affected the surface reaction layer formation. A thinner apatite layer was formed and was composed of a micro-porous layer comprising rounded particles in a glue

  19. Injectable calcium phosphate cement and fibrin sealant recombined human bone morphogenetic protein-2 composite in vertebroplasty: an animal study

    OpenAIRE

    Qian, Guang; Dong, Youhai; Yang, Wencheng; Wang, Minghai

    2012-01-01

    Polymethylmethacrylate (PMMA) is currently the most commonly-used material, but it may induce adjacent vertebral fracture due to low degradation and high strength. Our study evaluated the feasibility of injectable calcium phosphate cement (ICPC) and fibrin sealant (FS) as an injectable compound carrier of human bone morphogenetic protein-2 (rhBMP-2) in New Zealand rabbits for vertebroplasty. Results showed ICPC/FS/rhBMP-2 composites induced alkaline phosphatase most effectively at 2 and 4 wee...

  20. Influence of a dental ceramic and a calcium aluminate cement on dental biofilm formation and gingival inflammatory response

    OpenAIRE

    Konradsson, Katarina

    2007-01-01

    Dental restorative materials interact with their surrounding oral environment. Interaction factors can be release of toxic components and/or effects on biofilm formation and gingiva. In the end of the nineties, a calcium aluminate cement (CAC) was manufactured as a “bioceramic” alternative to resin composite. Dental ceramics are considered to be chemically stable and not to favour dental biofilm formation. Since the influence of aged, resin-bonded ceramic coverages is not fully investigated a...

  1. In Vitro Spectrophotometry of Tooth Discoloration Induced by Tooth-Colored Mineral Trioxide Aggregate and Calcium-Enriched Mixture Cement

    OpenAIRE

    Arman, Marjan; Khalilak, Zohreh; Rajabi, Moones; Esnaashari, Ehsan; Saati, Keyvan

    2015-01-01

    Introduction: There are numerous factors that can lead to tooth discoloration after endodontic treatment, such as penetration of endodontic materials into the dentinal tubules during root canal treatment. The aim of this in vitro study was to compare discoloration induced by tooth colored mineral trioxide aggregate (MTA) and calcium-enriched mixture (CEM) cement in extracted human teeth. Methods and Materials: Thirty two dentin-enamel cuboid blocks (7×7×2 mm) were prepared from extracted maxi...

  2. Current perspectives of bio-ceramic technology in endodontics: calcium enriched mixture cement - review of its composition, properties and applications

    OpenAIRE

    Utneja, Shivani; Nawal, Ruchika Roongta; Talwar, Sangeeta; Verma, Mahesh

    2014-01-01

    Advancements in bio-ceramic technology has revolutionised endodontic material science by enhancing the treatment outcome for patients. This class of dental materials conciliates excellent biocompatibility with high osseoconductivity that render them ideal for endodontic care. Few recently introduced bio-ceramic materials have shown considerable clinical success over their early generations in terms of good handling characteristics. Calcium enriched mixture (CEM) cement, Endosequence sealer, a...

  3. Low-pressure plasma treatment of polylactide fibers for enhanced mechanical performance of fiber-reinforced calcium phosphate cements

    OpenAIRE

    Canal Barnils, Cristina; Gallinetti, Sara; Ginebra Molins, Maria Pau

    2014-01-01

    Calcium phosphate cements (CPCs) are extensively used as synthetic bone grafts, but their poor mechanical properties limit their applicability to non-stress-bearing applications. The aim of the present work is to evaluate the potential of plasma surface modification of polylactide (PLA) fibers for reinforcement of CPCs. Oxygen low-pressure plasma was employed at different treatment times and the surface properties of the untreated and plasma-treated PLA were evaluated. Plasma treatment on the...

  4. Comparative evaluation of shear bond strength and microleakage of tricalcium silicate-based restorative material and radioopaque posterior glass ionomer restorative cement in primary and permanent teeth: An in vitro study

    Directory of Open Access Journals (Sweden)

    Vignesh Guptha Raju

    2014-01-01

    Full Text Available Background: Restoration of carious primary molars is still a major concern while treating the young children that too in deep carious lesion which extends below the cemento-enamel junction (CEJ where pulp protection and achieving adequate marginal seal are very important to prevent secondary caries. The needs were met with the development of new materials. One such of new bioactive material is tricalcium silicate-based restorative material (Biodentine, recommended for restoring deep lesions. Aim: To evaluate and compare shear bond strength and microleakage of tricalcium silicate-based restorative material (Biodentine and glass ionomer cement (Fuji IX GP in primary and permanent teeth. Materials and Methods: Occlusal surface of crowns were ground flat. PVC molds were stabilized over flat dentin surface and filled with tricalcium silicate-based restorative material (Biodentine/glass ionomer cement (Fuji IX GP according to group ascertained. Shear bond strength was evaluated using universal testing machine (INSTRON. Standardized Class II cavities were prepared on both primary and permanent teeth, and then restored with tricalcium silicate-based restorative material (Biodentine/glass ionomer cement (Fuji IX GP according to group ascertained, over which composite resin material was restored using an open sandwich technique. Microleakage was assessed using dye penetration. Microleakage was examined using a stereomicroscope. Results: Results showed that glass ionomer cement (Fuji IX GP exhibited better shear bond strength than tricalcium silicate-based restorative material (Biodentine. Mean microleakage score for glass ionomer cement (Fuji IX GP in permanent teeth was 1.52 and for primary teeth was 1.56. The mean microleakage for tricalcium silicate-based restorative material (Biodentine in permanent teeth was 0.76 and for primary teeth was 0.60. Glass ionomer cement (Fuji IX GP exhibited more microleakage than tricalcium silicate-based restorative

  5. Effect of polydopamine on the biomimetic mineralization of mussel-inspired calcium phosphate cement in vitro

    International Nuclear Information System (INIS)

    Inspired by the excellent adhesive property of mussel adhesive protein, we added polydopamine (PDA) to calcium phosphate cement (PDA–CPC) to enhance its compressive strength previously. The mineralization and mechanism on PDA–CPC were investigated by soaking it in simulated body fluid in this study. The results indicated that PDA promoted the conversion of dicalcium phosphate dihydrate and α-tricalcium phosphate to hydroxyapatite (HA) in the early stage but inhibited this conversion subsequently. PDA promoted the rapid mineralization on PDA–CPC to form a layer of nanoscale calcium phosphate (CaP) whereas there was no CaP formation on the control-CPC after 1 d of soaking. This layer of nanoscale CaP was similar to that of natural bone, which was always observed during soaking. X-ray photoelectron spectroscopy showed that the peak of C=O of PDA existed in the newly formed CaP on PDA–CPC, indicating the co-precipitation of CaP with PDA. Furthermore, the newly formed CaP on PDA–CPC was HA confirmed by transmission electron microscopy, which the newly formed HA was in association with PDA. Therefore, PDA increased the capacity of mineralization of CPC and induced the formation of nanoscale bone-like apatite on PDA–CPC. Thus, this provides the feasible route for surface modification on CPC. - Highlights: • Effect of polydopamine (PDA) on the in vitro mineralization of PDA-CPC was studied. • PDA promoted the rapid mineralization on PDA-CPC to form a nanoscale HA layer. • The precipitation of the nanoscale HA layer on PDA-CPC accompanied with PDA. • Polydopamine induced mineralization is feasible for surface modification of CaP

  6. Effect of polydopamine on the biomimetic mineralization of mussel-inspired calcium phosphate cement in vitro

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Zongguang [Key Lab of Advanced Technologies of Materials, Ministry of Education, School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China); Qu, Shuxin, E-mail: qushuxin@swjtu.edu.cn [Key Lab of Advanced Technologies of Materials, Ministry of Education, School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China); Zheng, Xiaotong; Xiong, Xiong [Key Lab of Advanced Technologies of Materials, Ministry of Education, School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China); Fu, Rong; Tang, Kuangyun; Zhong, Zhendong [Department of Plastic Surgery, Academy of Medical Sciences and Sichuan Provincial People' s Hospital, Chengdu 610041 (China); Weng, Jie [Key Lab of Advanced Technologies of Materials, Ministry of Education, School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031 (China)

    2014-11-01

    Inspired by the excellent adhesive property of mussel adhesive protein, we added polydopamine (PDA) to calcium phosphate cement (PDA–CPC) to enhance its compressive strength previously. The mineralization and mechanism on PDA–CPC were investigated by soaking it in simulated body fluid in this study. The results indicated that PDA promoted the conversion of dicalcium phosphate dihydrate and α-tricalcium phosphate to hydroxyapatite (HA) in the early stage but inhibited this conversion subsequently. PDA promoted the rapid mineralization on PDA–CPC to form a layer of nanoscale calcium phosphate (CaP) whereas there was no CaP formation on the control-CPC after 1 d of soaking. This layer of nanoscale CaP was similar to that of natural bone, which was always observed during soaking. X-ray photoelectron spectroscopy showed that the peak of C=O of PDA existed in the newly formed CaP on PDA–CPC, indicating the co-precipitation of CaP with PDA. Furthermore, the newly formed CaP on PDA–CPC was HA confirmed by transmission electron microscopy, which the newly formed HA was in association with PDA. Therefore, PDA increased the capacity of mineralization of CPC and induced the formation of nanoscale bone-like apatite on PDA–CPC. Thus, this provides the feasible route for surface modification on CPC. - Highlights: • Effect of polydopamine (PDA) on the in vitro mineralization of PDA-CPC was studied. • PDA promoted the rapid mineralization on PDA-CPC to form a nanoscale HA layer. • The precipitation of the nanoscale HA layer on PDA-CPC accompanied with PDA. • Polydopamine induced mineralization is feasible for surface modification of CaP.

  7. Effect of polymers on the nanostructure and on the carbonation of calcium silicate hydrates: a scanning transmission X-ray microscopy study

    KAUST Repository

    Ha, J.

    2011-09-07

    This study investigated the effects of organic polymers (polyethylene glycol and hexadecyltrimethylammonium) on structures of calcium silicate hydrates (C-S-H) which is the major product of Portland cement hydration. Increased surface areas and expansion of layers were observed for all organic polymer modified C-S-H. The results from attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopic measurements also suggest lowered water contents in the layered structures for the C-S-H samples that are modified by organic polymers. Scanning transmission X-ray microscopy (STXM) results further supports this observation. We also observed difference in the extent of C-S-H carbonation due to the presence of organic polymers. No calcite formed in the presence of HDTMA whereas formation of calcite was observed with C-S-H sample modified with PEG. We suggest that the difference in the carbonation reaction is possibly due to the ease of penetration and diffusion of the CO 2. This observation suggests that CO 2 reaction strongly depends on the presence of organic polymers and the types of organic polymers incorporated within the C-S-H structure. This is the first comprehensive study using STXM to quantitatively characterize the level of heterogeneity in cementitious materials at high spatial and spectral resolutions. The results from BET, XRD, ATR-FTIR, and STXM measurements are consistent and suggest that C-S-H layer structures are significantly modified due to the presence of organic polymers, and that the chemical composition and structural differences among the organic polymers determine the extent of the changes in the C-S-H nanostructures as well as the extent of carbonation reaction. © 2011 Springer Science+Business Media, LLC.

  8. Cross-linked chitosan improves the mechanical properties of calcium phosphate-chitosan cement.

    Science.gov (United States)

    Aryaei, Ashkan; Liu, Jason; Jayatissa, Ahalapitiya H; Champa Jayasuriya, A

    2015-09-01

    Calcium phosphate (CaP) cements are highly applicable and valuable materials for filling bone defects by minimally invasive procedures. The chitosan (CS) biopolymer is also considered as one of the promising biomaterial candidates in bone tissue engineering. In the present study, some key features of CaP-CS were significantly improved by developing a novel CaP-CS composite. For this purpose, CS was the first cross-linked with tripolyphosphate (TPP) and then mixed with CaP matrix. A group of CaP-CS samples without cross-linking was also prepared. Samples were fabricated and tested based on the known standards. Additionally, the effect of different powder (P) to liquid (L) ratios was also investigated. Both cross-linked and uncross-linked CaP-CS samples showed excellent washout resistance. The most significant effects were observed on Young's modulus and compressive strength in wet condition as well as surface hardness. In dry conditions, the Young's modulus of cross-linked samples was slightly improved. Based on the presented results, cross-linking does not have a significant effect on porosity. As expected, by increasing the P/L ratio of a sample, ductility and injectability were decreased. However, in the most cases, mechanical properties were enhanced. The results have shown that cross-linking can improve the mechanical properties of CaP-CS and hence it can be used for bone tissue engineering applications. PMID:26046262

  9. Enhancement of pedicle screw stability using calcium phosphate cement in osteoporotic vertebrae: in vivo biomechanical study.

    Science.gov (United States)

    Taniwaki, Yoshimichi; Takemasa, Ryuichi; Tani, Toshikazu; Mizobuchi, Hiroo; Yamamoto, Hiroshi

    2003-01-01

    We conducted an experimental study using female beagles with and without ovariectomy-induced osteoporosis to determine the effect of calcium phosphate cement (CPC) on the mechanical stability of inserted pedicle screws. A drill hole was created from the base of the transverse process to the vertebral body; CPC was injected into the hole, and then a screw was inserted into the same hole. In the presence of osteoporosis evidenced by dual X-ray absorptiometry, the stability of the inserted screw augmented by CPC against pull-out and cephalocaudal forces were significantly greater by 28% and 54% at 1 week after operation, 48% and 71% at 2 weeks, and 56% and 68% at 4 weeks compared with those without CPC. The pull-out strength increased progressively with time after surgery, probably reflecting new-bone growth from the surrounding cancellous bone, which was in direct contact with the CPC, as shown in the histologic study. At each time point the cephalocaudal rigidity was similar and the pull-out strength greater than that for the screws inserted without CPC in nonporotic dogs. These findings suggest that CPC augments the stability of the inserted pedicle screws and increases the stiffness of fixed osteoporotic motion segments using instrumentation. PMID:12768486

  10. Influence of artificially-induced porosity on the compressive strength of calcium phosphate bone cements.

    Science.gov (United States)

    Mouzakis, Dionysios; Zaoutsos, Stefanos Polymeros; Bouropoulos, Nikolaos; Rokidi, Stamatia; Papanicolaou, George

    2016-07-01

    The biological and mechanical nature of calcium phosphate cements (CPC's) matches well with that of bone tissues, thus they can be considered as an appropriate environment for bone repair as bone defect fillers. The current study focuses on the experimental characterization of the mechanical properties of CPCs that are favorably used in clinical applications. Aiming on evaluation of their mechanical performance, tests in compression loading were conducted in order to determine the mechanical properties of the material under study. In this context, experimental results occurring from the above mechanical tests on porous specimens that were fabricated from three different porous additives, namely albumin, gelatin and sodium alginate, are provided, while assessment of their mechanical properties in respect to the used porous media is performed. Additionally, samples reinforced with hydroxyapatite crystals were also tested in compression and the results are compared with those of the above tested porous CPCs. The knowledge obtained allows the improvement of their biomechanical properties by controlling their structure in a micro level, and finds a way to compromise between mechanical and biological response. PMID:26945808

  11. Solidification/stabilization of toxic metals in calcium aluminate cement matrices

    International Nuclear Information System (INIS)

    Highlights: • Reliable encapsulation and effective sorption of Pb, Zn and Cu on CAC was proved. • Cu and Pb were fully retained in the CAC mortar, while Zn was retained in 99.99%. •A maximum sorption capacity ca. 60 mg/g CAC was attained for Cu. • Three different PSD patterns were established as a function of XRD phase assemblage. • Some metal-loaded mortars achieved suitable mechanical strengths for landfilling. -- Abstract: The ability of calcium aluminate cement (CAC) to encapsulate toxic metals (Pb, Zn and Cu) was assessed under two curing conditions. Changes in the consistency and in the setting time were found upon the addition of the nitrates of the target metals. Both Pb and Cu caused a delay in CAC hydration, while Zn accelerated the stiffening of the mortar. Compressive strengths of the metal-doped mortars, when initially cured at 60 °C/100% RH, were comparable with that of the free-metal mortar. Three different pore size distribution patterns were identified and related to the compounds identified by XRD and SEM. Sorbent capacities of CAC for the toxic metals were excellent: a total uptake was achieved for up to 3 wt.% loading of the three metals. In this way, CAC mortars were perfectly able to encapsulate the toxic metals, allowing the use of CAC for waste management as proved by the leaching tests

  12. Stimulation of Odontogenesis and Angiogenesis via Bioactive Nanocomposite Calcium Phosphate Cements Through Integrin and VEGF Signaling Pathways.

    Science.gov (United States)

    Lee, Sang-Im; Lee, Eui-Suk; El-Fiqi, Ahmed; Lee, So-Youn; Eun-Cheol Kim; Kim, Hae-Won

    2016-05-01

    Formulating self-setting calcium phosphate cements (CPCs) with secondary phases particularly in the nanoscale order holds great promise to improve biological properties. Here, we focus on the effect that bioactive glass nanoparticles (BGN) incorporated in CPC compositions can have on the proliferation, odontogenic differentiation, and angiogenic stimulation of stem cells derived from human dental pulp (HDPSCs). These odontogenic and angiogenic events are of special importance in the dentin-pulp regeneration processes. In comparison to pure CPCs, nanocomposite cements exhibit a significantly improved proliferation of HDPSCs, and the improvement is more significant as the BGN content increases. The nanocomposite cements substantially enhance the adhesion of cells, and significantly up-regulate odontogenic differentiation, including alkaline phosphatase (ALP) activity and the expressions of odontogenic genes (sialophosphoprotein, dentin matrix protein I, ALP, osteopontin and osteocalcin). Furthermore, the use of nanocomposite cements result in stimulation of angiogenic gene expression (VEGF, FGF-2, VEGFRs, PECAM-1, and VE-cadherin) and protein production (VEGF, VEGFR-1). The angiogenic stimulation by the HDPSCs significantly affects the endothelial cell behaviors, that is, the endothelial cell migration and the tubular network formation are substantially improved when treated with HDPSC-conditioned medium, particularly with the help of nanocomposite cements. The integrin and VEGF signaling pathways are reasoned for the stimulation of the odontogenesis and angiogenesis of cells, where the nanocomposite cements up-regulate the integrin subsets α1, α2, α3, and β1, and activate the integrin downstream signal pathways, such as p-FAK, p-Akt, p-paxillin, JNK, EK, and NF-κB, as well as other nuclear transcriptional factors, including CREB, STAT-3, and ELK-1. The current results indicate that the new formulation of the nanocomposite self-setting cements might provide some

  13. Calcium silicate structure and carbonation shrinkage of a tobermorite-based material

    International Nuclear Information System (INIS)

    Carbonated autoclaved aerated concretes (AACs) show no shrinkage at a degree of carbonation approximately less than 20%. The 29Si MAS NMR spectrum showed that at a degree of carbonation less than 25%, the typical double-chain silicate anion structure of tobermorite-11A was well maintained and interlayer Ca ions were exchanged with protons. This corresponded to the absence of carbonation shrinkage at a degree of carbonation less than 20%. When the degree of carbonation increased from 25% to 50% up to 60%, the double-chain silicate anion structure of tobermorite-11A was decomposed and Ca ions in the Ca-O layers were dissolved, showing a possible mechanism of carbonation shrinkage

  14. Preparation and characterization of bioactive and degradable composites containing ordered mesoporous calcium-magnesium silicate and poly(L-lactide)

    International Nuclear Information System (INIS)

    Highlights: • Mesoporous calcium-magnesium silicate and poly(L-lactide) composite was fabricated. • The composite has good hydrophilicity, in vitro degradation and bioactivity. • The composite could support cell attachment, proliferation and differentiation. - Abstract: Polylactide (PLA) and its copolymers have been widely used for bone tissue regeneration. In this study, a bioactive composite of ordered mesoporous calcium–magnesium silicate (m-CMS) and poly(L-lactide) (PLLA) was fabricated by melt blending method. The results indicated that the m-CMS particles were entrapped by polymer phase, and crystallinity of PLLA significantly decreased while the thermal stability of the m-CMS/PLLA composites was not obviously affected by addition of the m-CMS into PLLA. In addition, compared to PLLA, incorporation of the m-CMS into PLLA significantly improved the hydrophilicity, in vitro degradability and bioactivity (apatite-formation ability) of the m-CMS/PLLA composite, which were m-CMS content dependent. Moreover, it was found that incorporation of the m-CMS into PLLA could neutralize the acidic degradation by-products and thus compensated for the decrease of pH value. In cell culture experiments, the results showed that the composite enhanced attachment, proliferation and alkaline phosphatase activity (ALP) of MC3T3-E1 cells, which were m-CMS content dependent. The results indicated that the addition of bioactive materials to PLLA could result in a composite with improved properties of hydrophilicity, degradability, bioactivity and cytocompatibility

  15. Preparation and characterization of bioactive and degradable composites containing ordered mesoporous calcium-magnesium silicate and poly(L-lactide)

    Energy Technology Data Exchange (ETDEWEB)

    Ji, Jiajin [Key Shanghai Key Laboratory of Advanced Polymeric Materials, East China University of Science and Technology, Shanghai 200237 (China); Dong, Xieping, E-mail: jxzhyxh@163.com [Department of Orthopaedic Surgery, Jiangxi People' s Hospital, Nanchang 330006 (China); Ma, Xuhui [Polymer Science (Shenzhen) New Materials Co., Ltd., Shenzhen 518101 (China); Tang, Songchao, E-mail: schtang@ecust.edu.cn [Key Shanghai Key Laboratory of Advanced Polymeric Materials, East China University of Science and Technology, Shanghai 200237 (China); Wu, Zhaoying; Xia, Ji; Wang, Quanxiang; Wang, Yutao; Wei, Jie [Key Shanghai Key Laboratory of Advanced Polymeric Materials, East China University of Science and Technology, Shanghai 200237 (China)

    2014-10-30

    Highlights: • Mesoporous calcium-magnesium silicate and poly(L-lactide) composite was fabricated. • The composite has good hydrophilicity, in vitro degradation and bioactivity. • The composite could support cell attachment, proliferation and differentiation. - Abstract: Polylactide (PLA) and its copolymers have been widely used for bone tissue regeneration. In this study, a bioactive composite of ordered mesoporous calcium–magnesium silicate (m-CMS) and poly(L-lactide) (PLLA) was fabricated by melt blending method. The results indicated that the m-CMS particles were entrapped by polymer phase, and crystallinity of PLLA significantly decreased while the thermal stability of the m-CMS/PLLA composites was not obviously affected by addition of the m-CMS into PLLA. In addition, compared to PLLA, incorporation of the m-CMS into PLLA significantly improved the hydrophilicity, in vitro degradability and bioactivity (apatite-formation ability) of the m-CMS/PLLA composite, which were m-CMS content dependent. Moreover, it was found that incorporation of the m-CMS into PLLA could neutralize the acidic degradation by-products and thus compensated for the decrease of pH value. In cell culture experiments, the results showed that the composite enhanced attachment, proliferation and alkaline phosphatase activity (ALP) of MC3T3-E1 cells, which were m-CMS content dependent. The results indicated that the addition of bioactive materials to PLLA could result in a composite with improved properties of hydrophilicity, degradability, bioactivity and cytocompatibility.

  16. Effect of different concentrations of potassium silicate, nano-silicon and calcium chloride on concentration of potassium, calcium and magnesium, chlorophyll content and number of florets of Asiatic lily cv. ‘Brunello’

    OpenAIRE

    N. Mirabbasi; A. Nikbakht; N. Etemadi; M.R. Sabzalian

    2013-01-01

    Production of many cut flowers, such as lilium, is very common in Iran. Flower quality has special importance in lilium flower production process, and proper nutrition is one of the major effective factors. This research was conducted to investigate the effect of different concentrations of potassium silicate, nano-silicon and calcium chloride on concentration of potassium, calcium and magnesium, chlorophyll index and number of florets of Asiatic lily 'Brunello'. The experiment was carried ou...

  17. Long-term heat storage in calcium sulfoaluminate cement (CSA) based concrete

    Energy Technology Data Exchange (ETDEWEB)

    Kaufmann, Josef P.; Winnefeld, Frank [Empa Swiss Federal Laboratories for Materials Science and Technology, Duebendorf (Switzerland). Lab. for Concrete and Construction Chemistry

    2011-07-01

    In general, the selection of materials proposed for solar heat storage is based on one of two principal processes: sensible heat storage or latent heat storage. Sensible heat storage utilizes the specific heat capacity of a material, while latent heat storage is based on the change in enthalpy (heat content) associated with a phase change of the material. Long time sensible heat storage requires excellent thermal insulation whereas latent heat storage allows permanent (seasonal) storage without significant energy losses and any special insulation. Ettringite, one of the cement hydration products, exhibits a high dehydration enthalpy. Calcium sulfoaluminate cement based concrete containing a high amount of ettringite is henceproposed as an efficient latent heat storage material. Compared to conventional heat storage materials this innovative concrete mixture has a high loss-free storage energy density (> 100-150 kWh/m{sup 3}) which is much higher than the one of paraffin or the (loss-sensitive) sensible heat of water. Like common concrete the CSA-concrete is stable and even may carry loads. The dehydration of the CSA-concrete is achieved at temperatures below 100 C. The rehydration process occurs as soon as water (liquid or vapor) is added. In contrast to paraffin, the phase change temperature is not fixed and the latent heat may be recovered at any desired temperature. Furthermore the heat conductivity of this material is high, so that the energy transfer from/to an exchange medium is easy. Additionally CSA-concrete is not flammable and absolutely safe regarding any health aspects. The cost of such CSA-concrete isin the order of normal concrete. The main application is seen in house heating systems. Solar heat, mostly generated during the summer period by means of roof collectors, can be stored in CSA-concrete until the winter. A part or even the whole annual heatingenergy may be produced and saved locally by the householder himself. Additional applications may be

  18. Effects of surface application of calcium-magnesium silicate and gypsum on soil fertility and sugarcane yield

    Directory of Open Access Journals (Sweden)

    Carlos Alexandre Costa Crusciol

    2014-12-01

    Full Text Available Lime application recommendations for amendment of soil acidity in sugarcane were developed with a burnt cane harvesting system in mind. Sugarcane is now harvested in most areas without burning, and lime application for amendment of soil acidity in this system in which the sugarcane crop residue remains on the ground has been carried out without a scientific basis. The aim of this study was to evaluate the changes in soil acidity and stalk and sugar yield with different rates of surface application of calcium, magnesium silicate, and gypsum in ratoon cane. The experiment was performed after the 3rd harvest of the variety SP 81-3250 in a commercial green sugarcane plantation of the São Luiz Sugar Mill (47º 25' 33" W; 21º 59' 46" S, located in Pirassununga, São Paulo, in southeast Brazil. A factorial arrangement of four Ca-Mg silicate rates (0, 850, 1700, and 3400 kg ha-1 and two gypsum rates (0 and 1700 kg ha-1 was used in the experiment. After 12 months, the experiment was harvested and technological measurements of stalk and sugar yield were made. After harvest, soil samples were taken at the depths of 0.00-0.05, 0.05-0.10, 0.10-0.20, 0.20-0.40, and 0.40-0.60 m in all plots, and the following determinations were made: soil pH in CaCl2, organic matter, P, S, K, Ca, Mg, H+Al, Al, Si, and base saturation. The results show that the application of gypsum reduced the exchangeable Al3+ content and Al saturation below 0.05 m, and increased the Ca2+ concentration in the whole profile, the Mg2+ content below 0.10 m, K+ below 0.4 m, and base saturation below 0.20 m. This contributed to the effect of surface application of silicate on amendment of soil acidity reaching deeper layers. From the results of this study, it may be concluded that the silicate rate recommended may be too low, since the greater rates used in this experiment showed greater reduction in soil acidity, higher levels of nutrients at greater depths and an increase in stalk and sugar

  19. Combined Percutaneous Iliosacral Screw Fixation With Sacroplasty Using Resorbable Calcium Phosphate Cement for Osteoporotic Pelvic Fractures Requiring Surgery.

    Science.gov (United States)

    Collinge, Cory A; Crist, Brett D

    2016-06-01

    Osteoporotic sacral fractures, including acute and chronic insufficiency fractures, are increasing in frequency and present a number of management problem. Many of these patients are treated nonoperatively with relative immobility (eg, bedrest, wheelchair, or weight-bearing restrictions) and analgesics, which likely make the osteoporotic component worse. Surgery in this patient population may be desirable in some cases with the goals of improving mobility, relieving pain, and healing in an aligned position while minimizing deformity progression. However, internal fixation of the osteoporotic pelvis can be difficult. Large unicortical lag screws are the workhorse of posterior pelvic fixation, and yet fixation in cancellous bone corridors of an osteoporotic sacrum seems unlikely to achieve optimal fixation. As a result, the operative management and clinical results of these difficult injuries may not be uniformly successful. The authors present a technique for treating osteoporotic patients with a sacral fracture when operative treatment is indicated using percutaneous screw fixation combined with screw augmentation using a resorbable calcium phosphate bone substitute or "cement." The guide wire for a 7.3-mm or other large cannulated lag screw is fully inserted along the desired bony sacral corridor as is standard. The lag screw is then inserted over the wire to the depth where cement is desired. The guide wire is removed, and the aqueous calcium phosphate is injected through the screw's cannulation. For acute fractures, cement was applied to the areas distant to the fracture; whereas in insufficiency fractures, the cement was inserted along most of the screw path. The guide wire then can be reinserted and the lag screw fully inserted. The rationale for using these 2 modalities is their synergistic effect: the cannulated screw provides typical screw fixation and also a conduit for cement application. The cement augments the lag screw's purchase in osteoporotic bone

  20. Rat subcutaneous tissue response to calcium silicate containing different arsenic concentrations

    Directory of Open Access Journals (Sweden)

    Paloma Gagliardi MINOTTI

    2015-02-01

    Full Text Available Objective: To evaluate the response of rat subcutaneous tissue in implanted polyethylene tubes that were filled with GMTA Angelus and Portland cements containing different arsenic concentrations. Material and Methods: Atomic absorption spectrophotometry was utilized to obtain the values of the arsenic concentration in the materials. Thirty-six rats were divided into 3 groups of 12 animals for each experimental period. Each animal received two implants of polyethylene tubes filled with different test cements and the lateral of the tubes was used as a control group. After 15, 30 and 60 days of implantation, the animals were killed and the specimens were prepared for descriptive and morphometric analysis considering: inflammatory cells, collagen fibers, fibroblasts, blood vessels and other components. The results were analyzed utilizing the Kuskal-Wallis test and the Dunn's Multiple test for comparison (p<0.05. Results: The materials showed, according to atomic absorption spectrophotometry, the following doses of arsenic: GMTA Angelus: 5.01 mg/kg, WPC Irajazinho: 0.69 mg/kg, GPC Minetti: 18.46 mg/kg and GPC Votoran: 10.76 mg/kg. In a 60-day periods, all specimens displayed a neoformation of connective tissue with a structure of fibrocellular aspect (capsule. Control groups and MTA Angelus produced the lower amount of inflammatory reaction and GPC Minetti, the highest reaction. Conclusions: There was no direct relationship between the concentration of arsenic present in the composition of the materials and the intensity of the inflammatory reactions. Higher values, as 18.46 mg/kg of arsenic in the cement, produce characteristics of severe inflammation reaction at the 60-day period. The best results were found in MTA angelus.

  1. Calcium phosphate cement delivering zoledronate decreases bone turnover rate and restores bone architecture in ovariectomized rats

    International Nuclear Information System (INIS)

    Patients sustaining bony fractures frequently require the application of bone graft substitutes to fill the bone defects. In the meantime, anti-osteoporosis drugs may be added in bone fillers to treat osteoporosis, especially in postmenopausal women and the elderly. The effects of zoledronate-impregnated calcium phosphate cement (ZLN/CPC) on ovariectomized (OVX) rats were evaluated. OVX rats were implanted with ZLN/CPC, containing 0.025 mg ZLN in the greater omentum. Afterward the clinical sign of toxicity was recorded for eight weeks. The rats were sacrificed and blood samples were collected for hematology and serum bone turnover markers analyses. The four limbs of the rats were harvested and micro-computer tomography (micro-CT) scanning and bone ash analyses were performed. No clinical toxicity was observed in the treated rats. Compared to the OVX rats, levels of bone resorption markers (fragments of C-telopeptides of type I collagen) and bone formation markers (alkaline phosphatase and osteocalcin) decreased significantly in the treated rats. Osteopontin, which mediates the anchoring of osteoclasts to the mineral matrix of bones, also decreased significantly. Micro-CT scanning and histologic examinations of the distal femoral metaphyses showed that the cancellous bone architectures were restored, with a concomitant decrease in bone porosity. The bone mineral content in the bone ashes also increased significantly. This study indicates that ZLN-impregnated CPC reduces bone turnover rate and restores bone architecture in OVX rats. CPC may be an appropriate carrier to deliver drugs to treat osteoporosis, and this approach may also reduce rates of post-dosing symptoms for intravenous ZLN delivery. (paper)

  2. Vascularization of plastic calcium phosphate cement in vivo induced by in-situ-generated hollow channels.

    Science.gov (United States)

    Yu, Tao; Dong, Chao; Shen, Zhonghua; Chen, Yan; Yu, Bo; Shi, Haishan; Zhou, Changren; Ye, Jiandong

    2016-11-01

    Despite calcium phosphate cement (CPC) is promising for bone repair therapy, slow biodegradation and insufficient vascularization in constructs negatively impacts its clinical application. A self-setting CPC composited with gelatin fiber is investigated to test the utility of this tissue engineering strategy to support rapid and extensive vascularization process. The interconnected hollow channels in CPC are formed after dissolution of gelatin fibers in vivo. The CPC-gelatin samples exhibit relatively decent/enhanced mechanical property, compared to the control. When implanted in vivo, the pre-established vascular networks in material anastomose with host vessels and accelerate vascular infiltration throughout the whole tissue construct. Different channel sizes induce different vascularization behaviors in vivo. Results indicate that the channel with the size of 250μm increases the expression of the representative angiogenic factors HIF1α, PLGF and migration factor CXCR4, which benefit the formation of small vessels. On the other hand, the channel with the size of 500μm enhances VEGF-A expression, which benefit the development of large vessels. Notably, the intersection area of channels has high invasive, sprouting and vasculogenesis potential under hypoxic condition, because more HIF1α-positive cells are observed there. Observation of the CD31-positive lumen in the border of scaffold indicates the ingrowth of blood vessels from its host into material through channel, benefited from gradually increased HIF1α expression. This kind of material was suggested to promote the effective application of bone regeneration through the combination of in situ self-setting, plasticity, angiogenesis, and osteoconductivity. PMID:27524007

  3. The biological performance of injectable calcium phosphate/PLGA cement in osteoporotic rats

    International Nuclear Information System (INIS)

    Calcium phosphate cements (CPCs) including poly(D,L-lactic-co-glycolic) acid (PLGA) microparticles are promising candidates for bone regenerative applications. Previous studies with CPC/PLGA demonstrated that the material is non-toxic, biocompatible and osteoconductive. However, the outcome of these studies was based on healthy individuals and consequently does not provide information on bone substitute material performance in a compromised situation, such as osteoporosis. Therefore, this study comparatively evaluated the performance of injectable CPC/PLGA in healthy (SHAM) and osteoporotic rats (OVX) using a rat femoral condyle defect with implantation periods of 4 and 12 weeks. It was hypothesized that in OVX rats the degradation of CPC/PLGA would increase due to a higher osteoclastic activity present in osteoporotic animals and that the obtained space would be rapidly filled with newly formed bone. The results revealed an accelerated degradation of the used CPC/PLGA in osteoporotic animals, but bone formation was less compared to that in healthy animals at 4 and 12 weeks after implantation. In addition, after 4 weeks, the amount of newly formed bone under osteoporotic conditions was less in the femoral condyle defect compared to that present in a non-defect, osteoporotic control femoral condyle, but equal after 12 weeks. On the other hand, in healthy animals, the amount of newly formed bone in the femoral condyle defect was equal to that present in a non-defect control femoral condyle at 4 weeks, while higher after 12 weeks. This indicates that bone regeneration at a defect site under osteoporotic conditions is slower, but can reach native amounts after longer time periods. Consequently, bone regenerative treatments under osteoporotic conditions seem to require additional empowerment of bone substitute materials. (paper)

  4. Effect of pH and Lidocaine on the Compressive Strength of Calcium Enriched Mixture Cement

    Directory of Open Access Journals (Sweden)

    Sobhnamayan F

    2015-12-01

    Full Text Available Statement of Problem: The pH of the human abscess has been measured as low as 5.0. This low pH could potentially inhibit setting reactions, affect adhesion, or increase the solubility of root end filling materials hence affect the compressive strength. Moreover, root end filling materials might expose or even mix with lidocaine HCL during periapical surgery. Objectives: The aim of this in vitro study was to evaluate the effect of acidic pH and lidocaine on the compressive strength of calcium-enriched mixture (CEM. Materials and Methods: CEM was mixed according to the manufacturer’s instructions or with lidocaine (L, and condensed into 6 × 4 mm split moulds. The samples were exposed to phosphate buffered saline (PBS at pH 5 or 7.4 for 7 or 28 days. Cylindrical blocks of CEM (total number = 120 and 15 for each group were subjected to compressive strength test using a universal testing machine. Data were analysed using three-factor analysis of variance (ANOVA. Results: Regardless of pH and time, significant differences were not found between lidocaine groups and the groups that were mixed according to the manufacturer’s instruction (p = 0.083. For both mixing agents, regardless of time, there were no significant differences between the two pH levels (p = 0.157. Regardless of the material and pH, there was a significant increase in the compressive strength from days 7 to 28 (p < 0.001. Conclusions: Mixtures with lidocaine and exposure to an acidic environment had no adverse effects on the compressive strength of CEM Cement.

  5. Induced Pluripotent Stem Cell-derived Mesenchymal Stem Cell Seeding on Biofunctionalized Calcium Phosphate Cements

    Institute of Scientific and Technical Information of China (English)

    WahWah TheinHan; Jun Liu; Minghui Tang; Wenchuan Chen; Linzhao Cheng; Hockin H. K. Xu

    2013-01-01

    Induced pluripotent stem cells (iPSCs) have great potential due to their proliferation and differentiation capability. The objectives of this study were to generate iPSC-derived mesenchymal stem cells (iPSC-MSCs), and investigate iPSC-MSC proliferation and osteogenic differentiation on calcium phosphate cement (CPC) containing biofunctional agents for the first time. Human iPSCs were derived from marrow CD34+ cells which were reprogrammed by a single episomal vector. iPSCs were cultured to form embryoid bodies (EBs), and MSCs migrated out of EBs. Five biofunctional agents were incorporated into CPC:RGD (Arg-Gly-Asp) peptides, fibronectin (Fn), fibronectin-like engineered polymer protein (FEPP), extracellular matrix Geltrex, and platelet concentrate. iPSC-MSCs were seeded on five biofunctionalized CPCs:CPC-RGD, CPC-Fn, CPC-FEPP, CPC-Geltrex, and CPC-Platelets. iPSC-MSCs on biofunctional CPCs had enhanced proliferation, actin fiber expression, osteogenic differentiation and mineralization, compared to control. Cell proliferation was greatly increased on biofunctional CPCs. iPSC-MSCs underwent osteogenic differentiation with increased alkaline phosphatase, Runx2 and collagen-I expressions. Mineral synthesis by iPSC-MSCs on CPC-Platelets was 3-fold that of CPC control. In conclusion, iPSCs showed high potential for bone engineering. iPSC-MSCs on biofunctionalized CPCs had cell proliferation and bone mineralization that were much better than traditional CPC. iPSC-MSC-CPC constructs are promising to promote bone regeneration in craniofacial/orthopedic repairs.

  6. Investigation of Pozzolanic Reaction in Nanosilica-Cement Blended Pastes Based on Solid-State Kinetic Models and 29Si MAS NMR

    Directory of Open Access Journals (Sweden)

    Jiho Moon

    2016-02-01

    Full Text Available The incorporation of pozzolanic materials in concrete has many beneficial effects to enhance the mechanical properties of concrete. The calcium silicate hydrates in cement matrix of concrete increase by pozzolanic reaction of silicates and calcium hydroxide. The fine pozzolanic particles fill spaces between clinker grains, thereby resulting in a denser cement matrix and interfacial transition zone between cement matrix and aggregates; this lowers the permeability and increases the compressive strength of concrete. In this study, Ordinary Portland Cement (OPC was mixed with 1% and 3% nanosilica by weight to produce cement pastes with water to binder ratio (w/b of 0.45. The specimens were cured for 7 days. 29Si nuclear magnetic resonance (NMR experiments are conducted and conversion fraction of nanosilica is extracted. The results are compared with a solid-state kinetic model. It seems that pozzolanic reaction of nanosilica depends on the concentration of calcium hydroxide.

  7. Development of a novel aluminum-free glass ionomer cement based on magnesium/strontium-silicate glasses

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Dong-Ae [Department of Biomaterials Science, College of Dentistry, Dankook University, Cheonan 330-714 (Korea, Republic of); Department of Nanobiomedical Science and BK21 Plus NBM Global Research Center for Regenerative Medicine, Dankook University Graduate School, Cheonan 330-714 (Korea, Republic of); Abo-Mosallam, Hany A. [Glass Research Department, National Research Centre, Dokki, Cairo (Egypt); Lee, Hye-Young [Department of Nanobiomedical Science and BK21 Plus NBM Global Research Center for Regenerative Medicine, Dankook University Graduate School, Cheonan 330-714 (Korea, Republic of); Institute of Tissue Regeneration Engineering (ITREN), Dankook University, Cheonan 330-714 (Korea, Republic of); Kim, Gyu-Ri [Department of Biomaterials Science, College of Dentistry, Dankook University, Cheonan 330-714 (Korea, Republic of); Department of Nanobiomedical Science and BK21 Plus NBM Global Research Center for Regenerative Medicine, Dankook University Graduate School, Cheonan 330-714 (Korea, Republic of); Kim, Hae-Won [Department of Biomaterials Science, College of Dentistry, Dankook University, Cheonan 330-714 (Korea, Republic of); Department of Nanobiomedical Science and BK21 Plus NBM Global Research Center for Regenerative Medicine, Dankook University Graduate School, Cheonan 330-714 (Korea, Republic of); Institute of Tissue Regeneration Engineering (ITREN), Dankook University, Cheonan 330-714 (Korea, Republic of); Lee, Hae-Hyoung, E-mail: haelee@dku.edu [Department of Biomaterials Science, College of Dentistry, Dankook University, Cheonan 330-714 (Korea, Republic of); Institute of Tissue Regeneration Engineering (ITREN), Dankook University, Cheonan 330-714 (Korea, Republic of)

    2014-09-01

    The effects of strontium substitution for magnesium in a novel aluminum-free multicomponent glass composition for glass ionomer cements (GICs) were investigated. A series of glass compositions were prepared based on SiO{sub 2}-P{sub 2}O{sub 5}-CaO-ZnO-MgO{sub (1-X)}-SrO{sub X}-CaF{sub 2} (X = 0, 0.25, 0.5 and 0.75). The mechanical properties of GICs prepared were characterized by compressive strength, flexural strength, flexural modules, and microhardness. Cell proliferation was evaluated indirectly by CCK-8 assay using various dilutions of the cement and rat mesenchyme stem cells. Incorporation of strontium instead of magnesium in the glasses has a significant influence on setting time of the cements and the properties. All mechanical properties of the GICs with SrO substitution at X = 0.25 were significantly increased, then gradually decreased with further increase of the amount of strontium substitution in the glass. The GIC at X = 0.25, also, showed an improved cell viability at low doses of the cement extracts in comparison with other groups or control without extracts. The results of this study demonstrate that the glass compositions with strontium substitution at low levels can be successfully used to prepare aluminum-free glass ionomer cements for repair and regeneration of hard tissues. - Highlights: • We developed multicomponent glass compositions for a novel aluminum-free glass ionomer cement (GIC). • The effects of MgO replacement with SrO in the glasses on the mechanical properties and cell proliferation were evaluated. • Substitution of MgO with SrO at low levels led to improvement of mechanical properties and cell viability of the cements. • Microstructural degradations in the cement matrix of the GICs with strontium at high levels were observed after aging.

  8. Development of a novel aluminum-free glass ionomer cement based on magnesium/strontium-silicate glasses

    International Nuclear Information System (INIS)

    The effects of strontium substitution for magnesium in a novel aluminum-free multicomponent glass composition for glass ionomer cements (GICs) were investigated. A series of glass compositions were prepared based on SiO2-P2O5-CaO-ZnO-MgO(1-X)-SrOX-CaF2 (X = 0, 0.25, 0.5 and 0.75). The mechanical properties of GICs prepared were characterized by compressive strength, flexural strength, flexural modules, and microhardness. Cell proliferation was evaluated indirectly by CCK-8 assay using various dilutions of the cement and rat mesenchyme stem cells. Incorporation of strontium instead of magnesium in the glasses has a significant influence on setting time of the cements and the properties. All mechanical properties of the GICs with SrO substitution at X = 0.25 were significantly increased, then gradually decreased with further increase of the amount of strontium substitution in the glass. The GIC at X = 0.25, also, showed an improved cell viability at low doses of the cement extracts in comparison with other groups or control without extracts. The results of this study demonstrate that the glass compositions with strontium substitution at low levels can be successfully used to prepare aluminum-free glass ionomer cements for repair and regeneration of hard tissues. - Highlights: • We developed multicomponent glass compositions for a novel aluminum-free glass ionomer cement (GIC). • The effects of MgO replacement with SrO in the glasses on the mechanical properties and cell proliferation were evaluated. • Substitution of MgO with SrO at low levels led to improvement of mechanical properties and cell viability of the cements. • Microstructural degradations in the cement matrix of the GICs with strontium at high levels were observed after aging

  9. Current perspectives of bio-ceramic technology in endodontics: calcium enriched mixture cement - review of its composition, properties and applications

    Science.gov (United States)

    Nawal, Ruchika Roongta; Talwar, Sangeeta; Verma, Mahesh

    2015-01-01

    Advancements in bio-ceramic technology has revolutionised endodontic material science by enhancing the treatment outcome for patients. This class of dental materials conciliates excellent biocompatibility with high osseoconductivity that render them ideal for endodontic care. Few recently introduced bio-ceramic materials have shown considerable clinical success over their early generations in terms of good handling characteristics. Calcium enriched mixture (CEM) cement, Endosequence sealer, and root repair materials, Biodentine and BioAggregate are the new classes of bio-ceramic materials. The aim of this literature review is to present investigations regarding properties and applications of CEM cement in endodontics. A review of the existing literature was performed by using electronic and hand searching methods for CEM cement from January 2006 to December 2013. CEM cement has a different chemical composition from that of mineral trioxide aggregate (MTA) but has similar clinical applications. It combines the biocompatibility of MTA with more efficient characteristics, such as significantly shorter setting time, good handling characteristics, no staining of tooth and effective seal against bacterial leakage. PMID:25671207

  10. Current perspectives of bio-ceramic technology in endodontics: calcium enriched mixture cement - review of its composition, properties and applications.

    Science.gov (United States)

    Utneja, Shivani; Nawal, Ruchika Roongta; Talwar, Sangeeta; Verma, Mahesh

    2015-02-01

    Advancements in bio-ceramic technology has revolutionised endodontic material science by enhancing the treatment outcome for patients. This class of dental materials conciliates excellent biocompatibility with high osseoconductivity that render them ideal for endodontic care. Few recently introduced bio-ceramic materials have shown considerable clinical success over their early generations in terms of good handling characteristics. Calcium enriched mixture (CEM) cement, Endosequence sealer, and root repair materials, Biodentine and BioAggregate are the new classes of bio-ceramic materials. The aim of this literature review is to present investigations regarding properties and applications of CEM cement in endodontics. A review of the existing literature was performed by using electronic and hand searching methods for CEM cement from January 2006 to December 2013. CEM cement has a different chemical composition from that of mineral trioxide aggregate (MTA) but has similar clinical applications. It combines the biocompatibility of MTA with more efficient characteristics, such as significantly shorter setting time, good handling characteristics, no staining of tooth and effective seal against bacterial leakage. PMID:25671207

  11. XANES analysis of calcium and sodium phosphates and silicates and hydroxyapatite-Bioglass (registered) 45S5 co-sintered bioceramics

    International Nuclear Information System (INIS)

    Bioglass (registered) 45S5 was co-sintered with hydroxyapatite at 1200 deg. C. When small amounts (5(PO4)2SiO4 and Na3Ca6(PO4)5 in an amorphous silicate matrix respectively. These chemistries show improved bioactivity compared to hydroxyapatite and are the subject of this study. The structure of several crystalline calcium and sodium phosphates and silicates as well as the co-sintered hydroxyapatite-Bioglass (registered) 45S5 bioceramics were examined using XANES spectroscopy. The nature of the crystalline and amorphous phases were studied using silicon (Si) and phosphorus (P) K- and L2,3-edge and calcium (Ca) K-edge XANES. Si L2,3-edge spectra of sintered bioceramic compositions indicates that the primary silicates present in these compositions are sodium silicates in the amorphous state. From Si K-edge spectra, it is shown that the silicates are in a similar structural environment in all the sintered bioceramic compositions with 4-fold coordination. Using P L2,3-edge it is clearly shown that there is no evidence of sodium phosphate present in the sintered bioceramic compositions. In the P K-edge spectra, the post-edge shoulder peak at around 2155 eV indicates that this shoulder to be more defined for calcium phosphate compounds with decreasing solubility and increasing thermodynamic stability. This shoulder peak is more noticeable in hydroxyapatite and β-TCP indicating greater stability of the phosphate phase. The only spectra that does not show a noticeable peak is the composition with Na3Ca6(PO4)5 in a silicate matrix indicating that it is more soluble compared to the other compositions.

  12. In situ X-ray pair distribution function analysis of accelerated carbonation of a synthetic calcium-silicate-hydrate gel

    Energy Technology Data Exchange (ETDEWEB)

    Morandeau, Antoine E.; White, Claire E. [Princeton

    2015-04-21

    Calcium–silicate–hydrate (C–S–H) gel is the main binder component in hydrated ordinary Portland cement (OPC) paste, and is known to play a crucial role in the carbonation of cementitious materials, especially for more sustainable alternatives containing supplementary cementitious materials. However, the exact atomic structural changes that occur during carbonation of C–S–H gel remain unknown. Here, we investigate the local atomic structural changes that occur during carbonation of a synthetic calcium–silicate–hydrate gel exposed to pure CO₂ vapour, using in situ X-ray total scattering measurements and subsequent pair distribution function (PDF) analysis. By analysing both the reciprocal and real-space scattering data as the C–S–H carbonation reaction progresses, all phases present during the reaction (crystalline and non-crystalline) have been identified and quantified, with the results revealing the emergence of several polymorphs of crystalline calcium carbonate (vaterite and calcite) in addition to the decalcified C–S–H gel. Furthermore, the results point toward residual calcium being present in the amorphous decalcified gel, potentially in the form of an amorphous calcium carbonate phase. As a result of the quantification process, the reaction kinetics for the evolution of the individual phases have been obtained, revealing new information on the rate of growth/dissolution for each phase associated with C–S–H gel carbonation. Moreover, the investigation reveals that the use of real space diffraction data in the form of PDFs enables more accurate determination of the phases that develop during complex reaction processes such as C–S–H gel carbonation in comparison to the conventional reciprocal space Rietveld analysis approach.

  13. Characterization of silicates and calcium carbonates applied to high-dose dosimetry

    International Nuclear Information System (INIS)

    The predominant isomorphous form in the biominerals studied in this work (oyster shell, coral, mother of pearl and shell) was aragonite. The appearance of the calcite phase occurred at 500 deg C at a heating rate of 10 deg C/s for all samples except for the coral sample, which was 400 deg C, independent of the heating rate. The most abundant element in the biominerals samples was Ca in the CaO form, and in the silicates (tremolite, diopside and rhodonite) Si in the SiO form. The most common trace element observed in the biominerals samples was Fe. The analyses of electron paramagnetic resonance showed lines of Mn2+ in the coral and mother-of-pearl samples before irradiation. In the case of the irradiated samples, the defects found were CO2-, CO33-, CO3- and SO2-, in the g range between 2.0010 and 2.0062. In the analyses by optical absorption of biominerals, transitions due to the presence of Mn in the samples were found. A thermoluminescent (TL) peak at approximately 140 deg C was found for the biominerals and at 180 deg C for silicates, which intensity depends directly on the dose. For samples exposed to different types of radiation, the TL peak occurred at lower temperatures. From the dose-response curves obtained for these materials, it was possible to determine a linear range for which their application in high dose dosimetry becomes possible. Taking into account the radiation type, among biominerals and silicates, the lowest detectable dose (40mGy) to gamma radiation was achieved for oyster shell samples using the measuring technique of optically stimulated luminescence (OSL). Using beta radiation, for diopside and tremolite samples the lowest detectable dose of 60mGy was obtained. For all samples, using the TL, OSL and thermally stimulated exoelectron emission (TSEE) techniques in alpha, beta and gamma radiation beans a good response reproducibility was obtained. Therefore, the samples characterized in this work are suitable to be used as high dose detectors

  14. Healing of segmental ulnar defects in dog using bioresorbable calcium phosphate cement added with recombinant human bone morphogenetic protein-2

    Energy Technology Data Exchange (ETDEWEB)

    Ohura, K.; Hamanishi, C. [Kinki Univ. School of Medicine, Osaka (Japan). Dept. of Orthopaedic Surgery; Irie, H. [Olympus Optical Co., Ltd., Tokyo (Japan)

    2001-07-01

    Bioresorbable calcium phosphate cement (BCPC) cylinders soaked with 100 {mu}g of rhBMP-2 were implanted into 21 mm segmental ulnar defects in dogs. New bone induced around cylinders united both bone segments in 3 weeks. As the cylinder dissolved, the induced bone was remodeled into the compact bone by 9 weeks. However, the cement cylinder implanted without BMP did not dissolve and that defect did not recover bone continuity in 9 weeks. Mechanical test at 9 weeks showed that the BMP group achieved 71% union and 63% of bone strength compared to normal ulna. However, other two groups, the implantation of the cylinder alone and no implantation, did not unite any case. The implantation of thin cylinders of BCPC soaked with small amount of rhBMP-2 repaired large bone defects of high mammal fast. Added with more BMP, it will be possible to apply this biocompatible composite even in clinical cases. (orig.)

  15. Immobilization of radioactive waste in cement-based matrices

    International Nuclear Information System (INIS)

    Tobermorite and xonotlite, two synthetic calcium silicate hydrates, improve the Cs retention of cement matrices for Cs, when incorporated at the 6 to 10% level. A kinetic and mechanistic scheme is presented for the reaction of fine grained, Cs-loaded clinoptilolite with cement. The Magnox waste form reacts quickly with cement, leading to an exchange of carbonate between waste form and cement components. Carbonation of cements leads to a marked improvement in their physical properties of Cs retentivity. Diffusion models are presented for cement systems whose variable parameters can readily be derived from experimental measurements. Predictions about scaled-up behaviour of large immobilized masses are applied to extrapolation of laboratory scale results to full-size masses. (author)

  16. Cement-Based Materials for Nuclear Waste Storage

    CERN Document Server

    Cau-di-Coumes, Céline; Frizon, Fabien; Lorente, Sylvie

    2013-01-01

    As the re-emergence of nuclear power as an acceptable energy source on an international basis continues, the need for safe and reliable ways to dispose of radioactive waste becomes ever more critical. The ultimate goal for designing a predisposal waste-management system depends on producing waste containers suitable for storage, transportation and permanent disposal. Cement-Based Materials for Nuclear-Waste Storage provides a roadmap for the use of cementation as an applied technique for the treatment of low- and intermediate-level radioactive wastes.Coverage includes, but is not limited to, a comparison of cementation with other solidification techniques, advantages of calcium-silicate cements over other materials and a discussion of the long-term suitability and safety of waste packages as well as cement barriers. This book also: Discusses the formulation and production of cement waste forms for storing radioactive material Assesses the potential of emerging binders to improve the conditioning of problemati...

  17. Effects of surface application of dolomitic limestone and calcium-magnesium silicate on soybean and maize in rotation with green manure in a tropical region

    Directory of Open Access Journals (Sweden)

    Gustavo Spadotti Amaral Castro

    2015-01-01

    Full Text Available Although lime is currently the material most frequently used to ameliorate soil acidity in Brazil, silicate could efficiently replace this source because of its greater solubility and its greater silicon content, which are beneficial for plant development. This study aimed to evaluate the effects of superficial lime and silicate application on soil chemical attributes as well as on soybean and maize nutrition and grain yields when these crops are grown in rotation with green manure. The experimental design was a complete randomized block with sixteen replicates. Plots were treated with one of two materials for acidity correction (dolomitic lime and calcium/magnesium silicate or with no soil correction, as a control. Silicate corrected soil acidity and increased exchangeable base levels in soil at greater depths faster than does liming. The application of both acidity-correcting materials increased N, Ca and Mg leaf concentrations, and all yield components and grain yield in soybean; but in maize, just silicate also increased N and Si when compared with lime, whereas both acidity-correcting increased just two yield components: grains per ear and mass of 100 grains, resulting in highest grain yield. The application of both acidity-correcting materials increased dry matter production of green manures, but for pigeon pea the silicate provided the best result in this dry-winter region.

  18. Different Angiogenic Abilities of Self-Setting Calcium Phosphate Cement Scaffolds Consisting of Different Proportions of Fibrin Glue

    OpenAIRE

    Jintao Xiu; Junjun Fan; Jie Li; Geng Cui; Wei Lei

    2014-01-01

    To investigate the different angiogenic abilities of the self-setting calcium phosphate cement (CPC) consisting of different proportions of fibrin glue (FG), the CPC powder and the FG solution were mixed at the powder/liquid (P/L) ratios of 1 : 0.5, 1 : 1, and 1 : 2 (g/mL), respectively, and pure CPC was used as a control. After being implanted into the lumbar dorsal fascia of the rabbit, the angiogenic process was evaluated by histological examination and CD31 immunohistochemistry to detect ...

  19. Calcium hydroxide poisoning

    Science.gov (United States)

    Hydrate - calcium; Lime milk; Slaked lime ... Calcium hydroxide ... These products contain calcium hydroxide: Cement Limewater Many industrial solvents and cleaners (hundreds to thousands of construction products, flooring strippers, brick cleaners, cement ...

  20. The suitability of a supersulfated cement for nuclear waste immobilisation

    Science.gov (United States)

    Collier, N. C.; Milestone, N. B.; Gordon, L. E.; Ko, S.-C.

    2014-09-01

    Composite cements based on ordinary Portland cement are used in the UK as immobilisation matrices for low and intermediate level nuclear wastes. However, the high pore solution pH causes corrosion of some metallic wastes and undesirable expansive reactions, which has led to alternative cementing systems being examined. We have investigated the physical, chemical and microstructural properties of a supersulfated cement in order to determine its applicability for use in nuclear waste encapsulation. The hardened supersulfated cement paste appeared to have properties desirable for use in producing encapsulation matrices, but the high powder specific surface resulted in a matrix with high porosity. Ettringite and calcium silicate hydrate were the main phases formed in the hardened cement paste and anhydrite was present in excess. The maximum rate of heat output during hydration of the supersulfated cement paste was slightly higher than that of a 9:1 blastfurnace slag:ordinary Portland cement paste commonly used by the UK nuclear waste processing industry, although the total heat output of the supersulfated cement paste was lower. The pH was also significantly lower in the supersulfated cement paste. Aluminium hydroxide was formed on the surface of aluminium metal encapsulated in the cement paste and ettringite was detected between the aluminium hydroxide and the hardened cement paste.

  1. Immobilization and leaching mechanisms of radwaste in cement-based matrices

    International Nuclear Information System (INIS)

    The effect of potential sorbers including silicas, titania, calcined kaolin, zirconium phosphate and two crystalline calcium silicates, tobermorite and xonotlite, have been used to improve the Cs-retention capacity of cement-based systems. The analysis of the pore fluid compositions of equilibrated cement-radwaste composites provides evidence concerning the leach mechanisms whereby Cs is removed. The reactions occurring between cement and clinoptilolite are elucidated and results of kinetic studies presented. Simulate Magnox waste is shown to react with cement, leading to a carbonate exchange. (author)

  2. The Early Strength of Slag Cements with Addition of Hydrate Microcrystals

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The effect of hydrate microcrystals such as calcium silicate hydrates (CSH) and ettringite on the early strength of slag cements was studied.The authors explored the possibility of improving the early strength of the slag cement by applying crystal seed technology.It is shown that slag crystal seeds make the early strength of the cement increased due to the action of hydrate crystal seeds,which speed up the hydration of clinker minerals in the nucleation of ettringite.Therefore,the early strength of the slag cement is obviously improved.

  3. Processing and characterisation of Calcium SulfoAluminate (CSA) eco-cements coated with a hybrid organo-inorganic material for photocatalytic applications

    OpenAIRE

    Morales-Cantero, Alejandro; Cabeza, Aurelio; De la Torre, Ángeles G.; Aranda, M. A. G.; Santacruz, Isabel

    2015-01-01

    On the one hand, Calcium SulfoAluminate (CSA) eco-cements are receiving increasing attention since their manufacture produces up to 40% less CO2 than ordinary Portland cement (OPC). In addition, they show interesting properties such as high early-age strengths, short setting times, impermeability, sulfate and chloride corrosion resistance and low alkalinity. On the other hand, water treatment is a key issue and it will become much more important in the decades ahead. We have developed a p...

  4. Local treatment of osteoporosis with alendronate-loaded calcium phosphate cement

    Institute of Scientific and Technical Information of China (English)

    Zhao Jindong; Tang Hai; Wang Jiayang; Li Gang

    2014-01-01

    Background A new treatment strategy is to target specific areas of the skeletal system that are prone to clinically significant osteoporotic fractures.We term this strategy as the "local treatment of osteoporosis".The study was performed to investigate the effect of alendronate-loaded calcium phosphate cement (CPC) as a novel drug delivery system for local treatment of osteoorosis.Methods An in vitro study was performed using CPC fabricated with different concentrations of alendronate (ALE,0,2,5,10 weight percent (wt%)).The microstructure,setting time,infrared spectrum,biomechanics,drug release,and biocompatibility of the composite were measured in order to detect changes when mixing CPC with ALE.An in vivo study was also performed using 30 Sprague-Dawley rats randomly divided into six groups:normal,Sham (ovariectomized (OVX) + Sham),CPC with 2% ALE,5%ALE,and 10% ALE groups.At 4 months after the implantation of the composite,animals were sacrificed and the caudal vertebrae (levels 4-7) were harvested for micro-CT examination and biomechanical testing.Results The setting time and strength of CPC was significantly faster and greater than the other groups.The ALE release was sustained over 21 days,and the composite showed good biocompatibility.In micro-CT analysis,compared with the Sham group,there was a significant increase with regard to volumetric bone mineral density (BMD) and trabecular number (Tb.N) in the treated groups (P <0.05).Trabecular spacing (Tb.Sp) showed a significant increase in the Sham group compared to other groups (P <0.01).However,trabecular thickness (Tb.Th) showed no significant difference among the groups.In biomechanical testing,the maximum compression strength and stiffness of trabecular bone in the Sham group were lower than those in the experimental groups.Conclusions The ALE-loaded CPC displayed satisfactory properties in vitro,which can reverse the OVX rat vertebral trabecular bone microarchitecture and biomechanical

  5. Influence of the redox state on the neptunium sorption under alkaline conditions. Batch sorption studies on titanium dioxide and calcium silicate hydrates

    Energy Technology Data Exchange (ETDEWEB)

    Tits, Jan; Laube, Andreas; Wieland, Erich [Paul Scherrer Institute (PSI), Villigen (Switzerland). Lab. for Waste Management; Gaona, Xavier [Karlsruhe Institute of Technology (KIT), Karlsruhe (Germany). Inst. for Nuclear Waste Disposal

    2014-07-01

    Wet chemistry experiments were carried out to investigate the effect of the redox state and aqueous speciation on the uptake of neptunium by titanium dioxide (TiO{sub 2}) and by calcium silicate hydrates (C-S-H) under alkaline conditions. TiO{sub 2} was chosen as a reference sorbent to determine the surface complexation behaviour of neptunium under alkaline conditions. C-S-H phases are important constituents of cement and concrete. They may contribute significantly to radionuclide retention due to their high recrystallization rates making incorporation the dominating sorption mechanism for many radionuclides (e.g. the actinides) on these materials. The sorption of neptunium on both solids was found to depend strongly on the degree of hydrolysis. On TiO{sub 2}R{sub d} values for Np(IV), Np(V) and Np(VI) are identical at pH = 10 and decrease with progressing hydrolysis in case of Np(V) and Np(VI). On C-S-H phases, R{sub d} values for the three redox states are also identical at pH = 10. While the R{sub d} values for Np(VI) sorption on C-S-H phases decrease with progressing hydrolysis, the R{sub d} values for Np(IV) and Np(V) sorption are not affected by the pH. In addition to the effect of hydrolysis, the presence of Ca is found to promote Np(V) and Np(VI) sorption on TiO{sub 2} whereas on C-S-H phases, the present wet chemistry data do not give unambiguous evidence. Thus, the aqueous speciation appears to have a similar influence on the sorption of the actinides on both types of solids despite the different sorption mechanism. The similar R{sub d} values for Np(IV,V,VI) sorption at pH = 10 can be explained qualitatively by invoking inter-ligand electrostatic repulsion between OH groups in the coordination sphere of Np(V) and Np(VI). This mechanism was proposed earlier in the literature for the prediction of actinide complexation constants with inorganic ligands. A limiting coordination number for each Np redox state, resulting from the inter-ligand electrostatic

  6. Influence of the redox state on the neptunium sorption under alkaline conditions. Batch sorption studies on titanium dioxide and calcium silicate hydrates

    International Nuclear Information System (INIS)

    Wet chemistry experiments were carried out to investigate the effect of the redox state and aqueous speciation on the uptake of neptunium by titanium dioxide (TiO2) and by calcium silicate hydrates (C-S-H) under alkaline conditions. TiO2 was chosen as a reference sorbent to determine the surface complexation behaviour of neptunium under alkaline conditions. C-S-H phases are important constituents of cement and concrete. They may contribute significantly to radionuclide retention due to their high recrystallization rates making incorporation the dominating sorption mechanism for many radionuclides (e.g. the actinides) on these materials. The sorption of neptunium on both solids was found to depend strongly on the degree of hydrolysis. On TiO2Rd values for Np(IV), Np(V) and Np(VI) are identical at pH = 10 and decrease with progressing hydrolysis in case of Np(V) and Np(VI). On C-S-H phases, Rd values for the three redox states are also identical at pH = 10. While the Rd values for Np(VI) sorption on C-S-H phases decrease with progressing hydrolysis, the Rd values for Np(IV) and Np(V) sorption are not affected by the pH. In addition to the effect of hydrolysis, the presence of Ca is found to promote Np(V) and Np(VI) sorption on TiO2 whereas on C-S-H phases, the present wet chemistry data do not give unambiguous evidence. Thus, the aqueous speciation appears to have a similar influence on the sorption of the actinides on both types of solids despite the different sorption mechanism. The similar Rd values for Np(IV,V,VI) sorption at pH = 10 can be explained qualitatively by invoking inter-ligand electrostatic repulsion between OH groups in the coordination sphere of Np(V) and Np(VI). This mechanism was proposed earlier in the literature for the prediction of actinide complexation constants with inorganic ligands. A limiting coordination number for each Np redox state, resulting from the inter-ligand electrostatic repulsion, allows the weaker sorption of the highest

  7. THERMOANALYTICAL EVENTS AND ENTHALPIES OF SELECTED PHASES AND SYSTEMS OF THE CHEMISTRY AND TECHNOLOGY OF CONCRETE PART I. CALCIUM-SILICATE-ALUMINATE-SULFATE HYDRATES

    OpenAIRE

    Milan Drabik; Lubica Galikova; Scholtzova Eva; Hadzimova Eva

    2014-01-01

    Essential focus of the study has been to acquire thermoanalytical events, incl. enthalpies of decompositions - (delta)H, of natural minerals of calcium-silicate-sulfate-aluminate hydrates. The thermoanalytical curves of thaumasite and ettringite are fully in line with that reported in reference sources. The values of (delta)H calculated from DSC curves in the intervals of key decomposition steps ranging from 50 to 250 C, achieve (1215 +/- 60) J g-1 for thaumasite and (930 +/- 40) J g...

  8. Biological Assessment of a Calcium Silicate Incorporated Hydroxyapatite-Gelatin Nanocomposite: A Comparison to Decellularized Bone Matrix

    Directory of Open Access Journals (Sweden)

    Dong Joon Lee

    2014-01-01

    Full Text Available Our laboratory utilized biomimicry to develop a synthetic bone scaffold based on hydroxyapatite-gelatin-calcium silicate (HGCS. Here, we evaluated the potential of HGCS scaffold in bone formation in vivo using the rat calvarial critical-sized defect (CSD. Twelve Sprague-Dawley rats were randomized to four groups: control (defect only, decellularized bone matrix (DECBM, and HGCS with and without multipotent adult progenitor cells (MAPCs. DECBM was prepared by removing all the cells using SDS and NH4OH. After 12 weeks, the CSD specimens were harvested to evaluate radiographical, histological, and histomorphometrical outcomes. The in vitro osteogenic effects of the materials were studied by focal adhesion, MTS, and alizarin red. Micro-CT analysis indicated that the DECBM and the HGCS scaffold groups developed greater radiopaque areas than the other groups. Bone regeneration, assessed using histological analysis and fluorochrome labeling, was the highest in the HGCS scaffold seeded with MAPCs. The DECBM group showed limited osteoinductivity, causing a gap between the implant and host tissue. The group grafted with HGCS+MAPCs resulting in twice as much new bone formation seems to indicate a role for effective bone regeneration. In conclusion, the novel HGCS scaffold could improve bone regeneration and is a promising carrier for stem cell-mediated bone regeneration.

  9. Biological assessment of a calcium silicate incorporated hydroxyapatite-gelatin nanocomposite: a comparison to decellularized bone matrix.

    Science.gov (United States)

    Lee, Dong Joon; Padilla, Ricardo; Zhang, He; Hu, Wei-Shou; Ko, Ching-Chang

    2014-01-01

    Our laboratory utilized biomimicry to develop a synthetic bone scaffold based on hydroxyapatite-gelatin-calcium silicate (HGCS). Here, we evaluated the potential of HGCS scaffold in bone formation in vivo using the rat calvarial critical-sized defect (CSD). Twelve Sprague-Dawley rats were randomized to four groups: control (defect only), decellularized bone matrix (DECBM), and HGCS with and without multipotent adult progenitor cells (MAPCs). DECBM was prepared by removing all the cells using SDS and NH4OH. After 12 weeks, the CSD specimens were harvested to evaluate radiographical, histological, and histomorphometrical outcomes. The in vitro osteogenic effects of the materials were studied by focal adhesion, MTS, and alizarin red. Micro-CT analysis indicated that the DECBM and the HGCS scaffold groups developed greater radiopaque areas than the other groups. Bone regeneration, assessed using histological analysis and fluorochrome labeling, was the highest in the HGCS scaffold seeded with MAPCs. The DECBM group showed limited osteoinductivity, causing a gap between the implant and host tissue. The group grafted with HGCS+MAPCs resulting in twice as much new bone formation seems to indicate a role for effective bone regeneration. In conclusion, the novel HGCS scaffold could improve bone regeneration and is a promising carrier for stem cell-mediated bone regeneration. PMID:25054149

  10. Anticorrosive effects and in vitro cytocompatibility of calcium silicate/zinc-doped hydroxyapatite composite coatings on titanium

    Science.gov (United States)

    Huang, Yong; Zhang, Honglei; Qiao, Haixia; Nian, Xiaofeng; Zhang, Xuejiao; Wang, Wendong; Zhang, Xiaoyun; Chang, Xiaotong; Han, Shuguang; Pang, Xiaofeng

    2015-12-01

    This work elucidated the corrosion resistance and cytocompatibility of electroplated Zn- and Si-containing bioactive calcium silicate/zinc-doped hydroxyapatite (ZnHA/CS) ceramic coatings on commercially pure titanium (CP-Ti). The formation of ZnHA/CS coating was investigated through Fourier transform infrared spectroscopy, X-ray diffraction (XRD), scanning electron microscopy, energy dispersive X-ray and inductively coupled plasma analyses. The XRD image showed that the reaction layer was mainly composed of HA and CaSiO3. The fabricated ZnHA/CS coatings presented a porous structure and appropriate thickness for possible applications in orthopaedic surgery. Potentiodynamic polarization tests showed that ZnHA/CS coatings exhibited higher corrosion resistance than CP-Ti. Dissolution tests on the coating also revealed that Si4+ and Zn2+ were leached at low levels. Moreover, MC3T3-E1 cells cultured on ZnHA/CS featured improved cell morphology, adhesion, spreading, proliferation and expression of alkaline phosphatase than those cultured on HA. The high cytocompatibility of ZnHA/CS could be mainly attributed to the combination of micro-porous surface effects and ion release (Zn2+ and Si4+). All these results indicate that ZnHA/CS composite-coated CP-Ti may be a potential material for orthopaedic applications.

  11. Synthesis and Enhanced Phosphate Recovery Property of Porous Calcium Silicate Hydrate Using Polyethyleneglycol as Pore-Generation Agent

    Directory of Open Access Journals (Sweden)

    Ling Pei

    2013-07-01

    Full Text Available The primary objective of this paper was to synthesize a porous calcium silicate hydrate (CSH with enhanced phosphate recovery property using polyethyleneglycol (PEG as pore-generation agent. The formation mechanism of porous CSH was proposed. PEG molecules were inserted into the void region of oxygen–silicon tetrahedron chains and the layers of CSH. A steric hindrance layer was generated to prevent the aggregation of solid particles. A porous structure was formed due to the residual space caused by the removal of PEG through incineration. This porous CSH exhibited highly enhanced solubility of Ca2+ and OH− due to the decreased particle size, declined crystalline, and increased specific surface area (SBET and pore volume. Supersaturation was increased in the wastewater with the enhanced solubility, which was beneficial to the formation of hydroxyapatite (HAP crystallization. Thus, phosphate can be recovered from wastewater by producing HAP using porous CSH as crystal seed. In addition, the regenerated phosphate-containing products (HAP can be reused to achieve sustainable utilization of phosphate. The present research could provide an effective approach for the synthesis of porous CSH and the enhancement of phosphate recovery properties for environmental applications.

  12. Photocatalytic NOx abatement by calcium aluminate cements modified with TiO2: Improved NO2 conversion

    International Nuclear Information System (INIS)

    Photocatalytic activity of TiO2 was studied in two types of calcium aluminate cement (CAC) under two different curing regimes. The effect of the TiO2 addition on the setting time, consistency and mechanical properties of the CACs was evaluated. The abatement of gaseous pollutants (NOx) under UV irradiation was also assessed. These cementitious matrices were found to successfully retain NO2: more abundant presence of aluminates in white cement (w-CAC, iron-lean) helped to better adsorb NO2, thus improving the conversion performance of the catalyst resulting in a larger NOx removal under UV irradiation. As evidenced by XRD, SEM, EDAX and zeta potential analyses, the presence of ferrite in dark cement (d-CAC, iron-reach) induced a certain chemical interaction with TiO2. The experimental findings suggest the formation of new iron titanate phases, namely pseudobrookite. The reduced band-gap energy of these compounds compared with that of TiO2 accounts for the photocatalytic activity of these samples

  13. Trials to solidify a Zn-containing low level radioactive sludge with calcium sulfo-aluminate cement

    International Nuclear Information System (INIS)

    It is well-known that Zn2+ acts as a strong retarder or even an inhibitor for the setting and hardening reaction of Portland cement. Calcium sulfo-aluminate (CSA) cement was expected to be the best solution to solidify the Zn-containing sludge in this study, because it generates an Ettringite-phase during hydration in which the Zn2+ can be integrated. With a commercially available CSA cement it was possible to develop recipes with a sufficient percentage of wet waste volume and a passable range of consistency for all existent water contents. The compressive strength of these recipes varied between 20 and 40 MPa depending on how much waste was in the recipe and how much water the waste contained. With water and sulfate resistance conforming to the guideline B05, the compressive strength was above the required 10 MPa in all cases. Additionally the linear expansion incl. layers was always clearly lower than the limiting 2%. The disadvantage of the recipes was superficial disintegration of the samples during leaching. One effect is that one can easily scrape off material from the surface of the samples, another is that flakes of material from the leached samples can be found on the bottom of leach bottles. For these reasons the development of a recipe for the solidification of the Zn-sludge is still a work in progress. (author)

  14. Influence of addition of calcium oxide on physicochemical properties of Portland cement with zirconium or niobium oxide

    Directory of Open Access Journals (Sweden)

    Mario Tanomaru-Filho

    2015-01-01

    Full Text Available Context: Calcium oxide (CaO may be added to mineral trioxide aggregate (MTA or Portland cement (PC to improve physicochemical and biological properties. Aims: To evaluate the physicochemical properties of PC associated with radiopacifiers and CaO. Materials and Methods: MTA Angelus, PC + 30% zirconium oxide (Zr, or 30% niobium oxide (Nb associated with 10 or 20% of CaO were evaluated. Gilmore needles were used to evaluate initial and final setting time. Compressive strength was evaluated after the periods of 24 hours and 21 days. pH was analyzed after 3, 12, 24 hours, 7, 14, 21 days. Solubility and flow tests were performed based on the ISO 6876. The data obtained were submitted to analysis of variance and Tukey tests (P ≤ 0.05. Results: The associations with 10% CaO showed greater strength that the associations with 20% CaO. The shortest initial setting time was observed for the association PC + Zr + 20% CaO and MTA. All the cements presented alkaline pH. The flow of all cements was similar. The highest solubility was found in the associations with 20% CaO. Conclusion: The addition of CaO to PC favored the alkaline property and the PC + Zr + 20% CaO presented setting time similar to MTA.

  15. Production and characterization of setting hydraulic cements based on calcium phosphate; Obtencao e caracterizacao de cimentos de fosfato de calcio de pega hidraulica

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Luci C. de; Rigo, Eliana C.S.; Santos, Luis A dos; Boschi, Anselmo Ortega [Sao Carlos Univ., SP (Brazil). Dept. de Engenharia de Materiais; Carrodeguas, Raul G. [Universidad de La Habana, Habana (Cuba). Centro de Biomateriales

    1997-12-31

    Setting hydraulic cements based on calcium phosphate has risen great interest in scientific literature during recent years due to their total bio compatibility and to the fact that they harden `in situ`, providing easy handling and adaptation to the shape and dimensions of the defect which requires correction, differently from the predecessors, the calcium phosphate ceramics (Hydroxy apatite, {beta}-tri calcium phosphate, biphasic, etc) in the shape of dense or porous blocks and grains. In the work, three calcium-phosphate cement compositions were studied. The resulting compositions were characterized according to the following aspects: setting times, pH, mechanical resistance, crystalline phases, microstructure and solubility in SBF (Simulated Body Fluid). The results show a potential use for the compositions. (author) 6 figs., 4 tabs.

  16. Dissolution kinetics of tuff rock and mechanism of chemical bond formation at the interface with cement grout

    International Nuclear Information System (INIS)

    The interaction of tuff rock and cement was studied to evaluate the effectiveness of sealing of tuff boreholes with cementitious grouts. Previous studies indicated chemical bond formation between tuff and cement. Dissolution studies were carried out on Topopah Spring member tuff and on tuff with cement. The results indicate the formation of calcium silicate and calcium aluminosilicate hydrates; phase identification is confirmed by XRD studies. The significance of the results obtained and their implications on properties of the interfacial region are included. 7 refs., 6 figs

  17. Hydrothermal synthesis and characterization of Si and Sr co-substituted hydroxyapatite nanowires using strontium containing calcium silicate as precursors

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Na [State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi Road, Shanghai 200050 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Zhai, Dong; Chen, Lei [State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi Road, Shanghai 200050 (China); Zou, Zhaoyong [State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi Road, Shanghai 200050 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Lin, Kaili, E-mail: lklsic@mail.sic.ac.cn [State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi Road, Shanghai 200050 (China); Chang, Jiang, E-mail: jchang@mail.sic.ac.cn [State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi Road, Shanghai 200050 (China)

    2014-04-01

    In the absence of any organic surfactants and solvents, the silicon (Si) and strontium (Sr) co-substituted hydroxyapatite [Ca{sub 10}(PO{sub 4}){sub 6}(OH){sub 2}, Si/Sr-HAp] nanowires were synthesized via hydrothermal treatment of the Sr-containing calcium silicate (Sr-CS) powders as the precursors in trisodium phosphate (Na{sub 3}PO{sub 4}) aqueous solution. The morphology, phase, chemical compositions, lattice constants and the degradability of the products were characterized. The Si/Sr-HAp nanowires with diameter of about 60 nm and up to 2 μm in length were obtained after hydrothermal treatment of the Sr-CS precursors. The Sr and Si substitution amount of the HAp nanowires could be well regulated by facile tailoring the Sr substitution level of the precursors and the reaction ratio of the precursor/solution, respectively. The SiO{sub 4} tetrahedra and Sr{sup 2+} ions occupied the crystal sites of the HAp, and the lattice constants increased apparently with the increase of the substitution amount. EDS mapping also suggested the uniform distribution of Si and Sr in the synthetic nanowires. Moreover, the Si/Sr-substitution apparently improved the degradability of the HAp materials. Our study suggested that the precursor transformation method provided a facile approach to synthesize the Si/Sr co-substituted HAp nanowires with controllable substitution amount, and the synthetic Si/Sr-HAp nanowires might be used as bioactive materials for hard tissue regeneration applications. - Highlights: • Si/Sr-HAp nanowires were hydrothermally transformed from Sr{sub x}-CaSiO{sub 3} precursors. • The Si/Sr-substitution level could be facilely regulated. • The nanowire-like morphology and composition could be simultaneously regulated.

  18. Hydrothermal synthesis and characterization of Si and Sr co-substituted hydroxyapatite nanowires using strontium containing calcium silicate as precursors

    International Nuclear Information System (INIS)

    In the absence of any organic surfactants and solvents, the silicon (Si) and strontium (Sr) co-substituted hydroxyapatite [Ca10(PO4)6(OH)2, Si/Sr-HAp] nanowires were synthesized via hydrothermal treatment of the Sr-containing calcium silicate (Sr-CS) powders as the precursors in trisodium phosphate (Na3PO4) aqueous solution. The morphology, phase, chemical compositions, lattice constants and the degradability of the products were characterized. The Si/Sr-HAp nanowires with diameter of about 60 nm and up to 2 μm in length were obtained after hydrothermal treatment of the Sr-CS precursors. The Sr and Si substitution amount of the HAp nanowires could be well regulated by facile tailoring the Sr substitution level of the precursors and the reaction ratio of the precursor/solution, respectively. The SiO4 tetrahedra and Sr2+ ions occupied the crystal sites of the HAp, and the lattice constants increased apparently with the increase of the substitution amount. EDS mapping also suggested the uniform distribution of Si and Sr in the synthetic nanowires. Moreover, the Si/Sr-substitution apparently improved the degradability of the HAp materials. Our study suggested that the precursor transformation method provided a facile approach to synthesize the Si/Sr co-substituted HAp nanowires with controllable substitution amount, and the synthetic Si/Sr-HAp nanowires might be used as bioactive materials for hard tissue regeneration applications. - Highlights: • Si/Sr-HAp nanowires were hydrothermally transformed from Srx-CaSiO3 precursors. • The Si/Sr-substitution level could be facilely regulated. • The nanowire-like morphology and composition could be simultaneously regulated

  19. Preparation and luminescence characteristics of Eu-doped calcium chloride silicate Ca7Si2O8Cl6

    International Nuclear Information System (INIS)

    Highlights: • Ca7Si2O8Cl6: Eu prepared in a reducing atmosphere contains Eu2+ and Eu3+ centers. • With increasing Eu-doping Eu2+ emission decrease and Eu3+ f–f transitions increase. • Luminescence color can be tunable Upon an excitation with near UV-light. • QE of Ca7Si2O8Cl6: 0.04Eu is 47.5% under excitation of 390 nm. -- Abstract: Eu-activated (0.1–5.0 mol%) calcium chloride silicate Ca7Si2O8Cl6 phosphors were prepared by means of ceramic method, which were characterized by X-ray powder diffraction and SEM measurements. The luminescence properties were investigated by the photoluminescence excitation and emission spectra, the luminescence decay lifetimes, the color coordinates and the internal quantum efficiency. Ca7Si2O8Cl6:Eu contains two kinds of Eu-emission centers, i.e., Eu2+ and Eu3+ ions, even it was prepared in a reducing atmosphere. Eu2+ and Eu3+ ions which present the characteristic broad band (5d → 4f) and narrow 4f → 4f luminescent features, respectively. The luminescence mechanism was discussed by analyzing the spectra, concentration-dependent emission intensity and lifetimes. With increasing Eu-doping, the energy transfer happens from Eu2+ to Eu3+ centers. Upon an excitation with near UV light, the luminescence color can be tunable from green to orange with increasing the Eu-doping because of the changes of the luminescence components from Eu3+ and Eu2+ ions in Ca7Si2O8Cl6 host. This is a potential phosphor combining both luminescence effects of Eu2+ and Eu3+ ions

  20. Functionalized calcium silicate nanofibers with hierarchical structure derived from oyster shells and their application in heavy metal ions removal.

    Science.gov (United States)

    You, Weijie; Hong, Mingzhu; Zhang, HaiFeng; Wu, Qiuping; Zhuang, Zanyong; Yu, Yan

    2016-06-21

    Inorganic hierarchical nanostructures have remarkable potential applications in environmental metal remediation; however, their applications usually suffer from low capacity, high cost, and difficulties in the recycling of adsorbents. We previously reported a facile strategy to synthesize acid-insoluble calcium silicate hydrates (CSH) from oyster shells, a representative kind of biowaste. However, little is known of the structure, size, and morphology of the as-prepared CSH, which hampers the improvement of their adsorption capacities. In this work, systematic investigation of the structures of as-generated CSH demonstrate that they have a hierarchically porous structure composed of thin nano-sheets, where each nano-sheet is assembled by nano-fibers with width of around ten nanometers. The hierarchical nanostructures with pore size of ∼12 nm provide a significant amount of active sites to graft polyethyleneimine (PEI), which enables the efficient extraction of both Cu(ii) cations and Cr(vi) anions from the aqueous solution. Batch experiments further indicate that the PEI-modified PCSH exhibit a maximum adsorption capacity of 203 and 256 mg g(-1) for Cu(ii) and Cr(vi), respectively, much higher than that of CSH, OS and many other adsorbents in literature. The adsorption of Cu(ii) and Cr(vi) proved to be spontaneous and exothermic. Combining the pH-dependent experiments with X-ray photoelectron spectroscopy analysis, the underlying mechanism is discussed. PCSH derived from OS biowaste maintains an efficient extraction ability toward Cu(ii) and Cr(vi) after five adsorption-desorption cycles. It is also applicable for treating various kinds of heavy metal ions and organic pollutants, showing potentially wide applications in water treatment. PMID:27221228

  1. Preparation and Evaluation of Solid Dispersion Tablets by a Simple and Manufacturable Wet Granulation Method Using Porous Calcium Silicate.

    Science.gov (United States)

    Fujimoto, Yumi; Hirai, Nobuaki; Takatani-Nakase, Tomoka; Takahashi, Koichi

    2016-01-01

    The aim of this study was to prepare and evaluate solid dispersion tablets containing a poorly water-soluble drug using porous calcium silicate (PCS) by a wet granulation method. Nifedipine (NIF) was used as the model poorly water-soluble drug. Solid dispersion tablets were prepared with the wet granulation method using ethanol and water by a high-speed mixer granulator. The binder and disintegrant were selected from 7 and 4 candidates, respectively. The dissolution test was conducted using the JP 16 paddle method. The oral absorption of NIF was studied in fasted rats. Xylitol and crospovidone were selected as the binder and disintegrant, respectively. The dissolution rates of NIF from solid dispersion formulations were markedly enhanced compared with NIF powder and physical mixtures. Powder X-ray diffraction (PXRD) confirmed the reduced crystallinity of NIF in the solid dispersion formulations. Fourier transform infrared (FT-IR) showed the physical interaction between NIF and PCS in the solid dispersion formulations. NIF is present in an amorphous state in granules prepared by the wet granulation method using water. The area under the plasma concentration-time curve (AUC) and peak concentration (Cmax) values of NIF after dosing rats with the solid dispersion granules were significantly greater than those after dosing with NIF powder. The solid dispersion formulations of NIF prepared with PCS using the wet granulation method exhibited accelerated dissolution rates and superior oral bioavailability. This method is very simple, and may be applicable to the development of other poorly water-soluble drugs. PMID:27039831

  2. Different response of osteoblastic cells to Mg(2+), Zn(2+) and Sr(2+) doped calcium silicate coatings.

    Science.gov (United States)

    Hu, Dandan; Li, Kai; Xie, Youtao; Pan, Houhua; Zhao, Jun; Huang, Liping; Zheng, Xuebin

    2016-03-01

    Mg(2+), Zn(2+) and Sr(2+) substitution for Ca(2+) in plasma sprayed calcium silicate (Ca-Si) coatings have been reported to impede their degradation in physiological environment and, more importantly, to improve their biological performance. The reason for the improved biological performance is still elusive and, especially, the contribution of the dopant ions is lack of obvious and direct evidence. In this study, we aim to identify the effect of Mg(2+), Zn(2+) and Sr(2+) incorporation on the osteogenic ability of Ca-Si based coatings (Ca2MgSi2O7, Ca2ZnSi2O7 and Sr-CaSiO3) by minimizing the influence of Ca and Si ions release and surface physical properties. Similar surface morphology, crystallinity and roughness were achieved for all samples by optimizing the spray parameters. As expected, Ca and Si ions release from all the coatings showed the comparable concentration with immersing time. The response of MC3T3-E1 cells onto Mg(2+), Zn(2+) and Sr(2+) doped Ca-Si coatings were studied in terms of osteoblastic adhesion, proliferation, differentiation and mineralization. The results showed that the level of cell adhesion and proliferation increased the most on the surface of Mg-modified coating. Gene expressions of early markers of osteoblast differentiation (COL-I and ALP mRNA) were obviously improved on Zn-modified coating. Gene expressions of later markers for osteoblast differentiation (OPN and OC mRNA) and mineralized nodules formation were obviously accelerated on the surface of Sr-modified coating. Since Mg(2+), Zn(2+) and Sr(2+) play a regulatory role in different stages of osteogenesis, it may be possible to utilize this in the development of new coating materials for orthopedic application. PMID:26787488

  3. XANES analysis of calcium and sodium phosphates and silicates and hydroxyapatite-Bioglass (registered) 45S5 co-sintered bioceramics

    Energy Technology Data Exchange (ETDEWEB)

    Demirkiran, Hande [Graduate Student, Materials Science and Engineering Department, University of Texas at Arlington, Arlington, TX (United States); Hu Yongfeng; Zuin, Lucia [Beamline Scientist, Canadian Light Source, Saskatoon, SK (Canada); Appathurai, Narayana [Beamline Scientist, Synchrotron Radiation Center, Madison, WI (United States); Aswath, Pranesh B., E-mail: aswath@uta.edu [Materials Science and Engineering Department, University of Texas at Arlington, Arlington, TX (United States)

    2011-03-12

    Bioglass (registered) 45S5 was co-sintered with hydroxyapatite at 1200 deg. C. When small amounts (< 5 wt.%) of Bioglass (registered) 45S5 was added it behaved as a sintering aid and also enhanced the decomposition of hydroxyapatite to {beta}-tricalcium phosphate. However when 10 wt.% and 25 wt.% Bioglass (registered) 45S5 was used it resulted in the formation of Ca{sub 5}(PO{sub 4}){sub 2}SiO{sub 4} and Na{sub 3}Ca{sub 6}(PO{sub 4}){sub 5} in an amorphous silicate matrix respectively. These chemistries show improved bioactivity compared to hydroxyapatite and are the subject of this study. The structure of several crystalline calcium and sodium phosphates and silicates as well as the co-sintered hydroxyapatite-Bioglass (registered) 45S5 bioceramics were examined using XANES spectroscopy. The nature of the crystalline and amorphous phases were studied using silicon (Si) and phosphorus (P) K- and L{sub 2,3}-edge and calcium (Ca) K-edge XANES. Si L{sub 2,3}-edge spectra of sintered bioceramic compositions indicates that the primary silicates present in these compositions are sodium silicates in the amorphous state. From Si K-edge spectra, it is shown that the silicates are in a similar structural environment in all the sintered bioceramic compositions with 4-fold coordination. Using P L{sub 2,3}-edge it is clearly shown that there is no evidence of sodium phosphate present in the sintered bioceramic compositions. In the P K-edge spectra, the post-edge shoulder peak at around 2155 eV indicates that this shoulder to be more defined for calcium phosphate compounds with decreasing solubility and increasing thermodynamic stability. This shoulder peak is more noticeable in hydroxyapatite and {beta}-TCP indicating greater stability of the phosphate phase. The only spectra that does not show a noticeable peak is the composition with Na{sub 3}Ca{sub 6}(PO{sub 4}){sub 5} in a silicate matrix indicating that it is more soluble compared to the other compositions.

  4. Effect of curing conditions on the dimensional and thermal stability of calcium phosphate cement for elevated temperature applications

    International Nuclear Information System (INIS)

    Calcium phosphate cements (CPCs) are attractive materials for elevated temperature applications, like moulds to process thermoplastics up to 300 °C. The CPC resulting from the reaction of wollastonite with phosphoric acid cured at room temperature however contains hydrated phases like brushite, and is thus not stable when exposed to temperatures above 200 °C. A non-contact method based on digital image correlation demonstrated that isothermal curing at 60 °C reduces the thermal shrinkage up to 300 °C by 25%. This curing method results in the direct formation of the more stable monetite in a shorter curing time. The correlated results of TGA, pH of the filtration water, and DSC analysis on partially cured material indicate this. XRD diffractograms and SEM images in combination with EDX show the evolution of the transformation of wollastonite into monetite, and the structure and morphology of the formed material

  5. Effect of curing conditions on the dimensional and thermal stability of calcium phosphate cement for elevated temperature applications

    Energy Technology Data Exchange (ETDEWEB)

    Blom, Johan [Vrije Universiteit Brussel, Department of Mechanics of Materials and Constructions, Pleinlaan 2, Brussels 1050 (Belgium); Rahier, Hubert [Vrije Universiteit Brussel, Research Group of Physical Chemistry and Polymer Sciences, Pleinlaan 2, Brussels 1050 (Belgium); Wastiels, Jan, E-mail: Jan.Wastiels@vub.ac.be [Vrije Universiteit Brussel, Department of Mechanics of Materials and Constructions, Pleinlaan 2, Brussels 1050 (Belgium)

    2014-12-15

    Calcium phosphate cements (CPCs) are attractive materials for elevated temperature applications, like moulds to process thermoplastics up to 300 °C. The CPC resulting from the reaction of wollastonite with phosphoric acid cured at room temperature however contains hydrated phases like brushite, and is thus not stable when exposed to temperatures above 200 °C. A non-contact method based on digital image correlation demonstrated that isothermal curing at 60 °C reduces the thermal shrinkage up to 300 °C by 25%. This curing method results in the direct formation of the more stable monetite in a shorter curing time. The correlated results of TGA, pH of the filtration water, and DSC analysis on partially cured material indicate this. XRD diffractograms and SEM images in combination with EDX show the evolution of the transformation of wollastonite into monetite, and the structure and morphology of the formed material.

  6. Stabilization/solidification of hazardous and radioactive wastes with alkali-activated cements

    International Nuclear Information System (INIS)

    This paper reviews progresses on the use of alkali-activated cements for stabilization/solidification of hazardous and radioactive wastes. Alkali-activated cements consist of an alkaline activator and cementing components, such as blast furnace slag, coal fly ash, phosphorus slag, steel slag, metakaolin, etc., or a combination of two or more of them. Properly designed alkali-activated cements can exhibit both higher early and later strengths than conventional portland cement. The main hydration product of alkali-activated cements is calcium silicate hydrate (C-S-H) with low Ca/Si ratios or aluminosilicate gel at room temperature; C-S-H, tobmorite, xonotlite and/or zeolites under hydrothermal condition, no metastable crystalline compounds such as Ca(OH)2 and calcium sulphoaluminates exist. Alkali-activated cements also exhibit excellent resistance to corrosive environments. The leachability of contaminants from alkali-activated cement stabilized hazardous and radioactive wastes is lower than that from hardened portland cement stabilized wastes. From all these aspects, it is concluded that alkali-activated cements are better matrix for solidification/stabilization of hazardous and radioactive wastes than Portland cement

  7. 水化硅酸钙的制备及磷回收性能表征%Preparation and phosphorus recovery performance of calcium silicate hydrate

    Institute of Scientific and Technical Information of China (English)

    关伟; 吉芳英; 陈晴空; 晏鹏; 张千

    2012-01-01

    Calcium silicate hydrate with phosphorus recovery efficiency was synthesized by carbide residue and silica. Effect of prepared method on phosphorus recovery efficiency of calcium silicate hydrate was studied. Mechanism of phosphorus recovery was revealed by XRD. Microstructure of calcium silicate hydrate was characterized by BET and SEM. Capacity of Ca^2+ and OH release was investigated. The considerable preparation conditions are obtained on the condition of Ca/Si molar ratio 1.6 - 1, reaction temperature 170℃, reaction time 4.5h, stirring intensity 90r/min. Phosphorus content of product of phosphorus recovery reached 18.64. The prepared calcium silicate hydrate has a high BET surface area 113. 3572m^2/g with porous structure. Concentration of Ca^2+ release reached 3.52mg/g. This material could recover phosphorus from wastewater in the form of hydroxyl calcium phosphate on the condition of pH=9.%以电石渣和白碳黑分别作为钙质和硅质原料,采用水热法制备具有磷回收特性的水化硅酸钙。研究了制备条件对水化硅酸钙磷回收性能的影响,采用XRD揭示了水化硅酸钙的磷回收机制。通过BET、SEM表征了水化硅酸钙的微观结构,考察了水化硅酸钙的溶钙供碱能力。钙硅摩尔比为1.6∶1,水热反应温度为170℃,水热反应时间为4.5h,搅拌强度为90r/min的条件下所制备的水化硅酸钙,其磷回收产品中的磷含量达到18.64%。该材料具有多孔结构,比表面积达到113.3572m2/g,能够溶出的Ca2+浓度为3.52mg/g,这些溶钙供碱特性使得该材料能够在pH值=9.0的环境下以羟基磷酸钙的形式从污水中回收磷。

  8. The suitability of a supersulfated cement for nuclear waste immobilisation

    Energy Technology Data Exchange (ETDEWEB)

    Collier, N.C., E-mail: nick.collier@sheffield.ac.uk [Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield, Mappin Street, Sheffield S1 3JD (United Kingdom); Milestone, N.B. [Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield, Mappin Street, Sheffield S1 3JD (United Kingdom); Callaghan Innovation, 69 Gracefield Road, PO Box 31310, Lower Hutt 5040 (New Zealand); Gordon, L.E. [Immobilisation Science Laboratory, Department of Materials Science and Engineering, The University of Sheffield, Mappin Street, Sheffield S1 3JD (United Kingdom); Geopolymer and Minerals Processing Group, Department of Chemical and Biomolecular Engineering, University of Melbourne, Parkville, Victoria 3010 (Australia); Ko, S.-C. [Holcim Technology Ltd, Hagenholzstrasse 85, CH-8050 Zurich (Switzerland)

    2014-09-15

    Highlights: • We investigate a supersulfated cement for use as a nuclear waste encapsulant. • High powder fineness requires a high water content to satisfy flow requirements. • Heat generation during hydration is similar to a control cement paste. • Typical hydration products are formed resulting in a high potential for waste ion immobilisation. • Paste pH and aluminium corrosion is less than in a control cement paste. - Abstract: Composite cements based on ordinary Portland cement are used in the UK as immobilisation matrices for low and intermediate level nuclear wastes. However, the high pore solution pH causes corrosion of some metallic wastes and undesirable expansive reactions, which has led to alternative cementing systems being examined. We have investigated the physical, chemical and microstructural properties of a supersulfated cement in order to determine its applicability for use in nuclear waste encapsulation. The hardened supersulfated cement paste appeared to have properties desirable for use in producing encapsulation matrices, but the high powder specific surface resulted in a matrix with high porosity. Ettringite and calcium silicate hydrate were the main phases formed in the hardened cement paste and anhydrite was present in excess. The maximum rate of heat output during hydration of the supersulfated cement paste was slightly higher than that of a 9:1 blastfurnace slag:ordinary Portland cement paste commonly used by the UK nuclear waste processing industry, although the total heat output of the supersulfated cement paste was lower. The pH was also significantly lower in the supersulfated cement paste. Aluminium hydroxide was formed on the surface of aluminium metal encapsulated in the cement paste and ettringite was detected between the aluminium hydroxide and the hardened cement paste.

  9. Injectable citrate-modified Portland cement for use in vertebroplasty.

    Science.gov (United States)

    Wynn-Jones, Gareth; Shelton, Richard M; Hofmann, Michael P

    2014-11-01

    The injectability of Portland cement (PC) with several citrate additives was investigated for use in clinical applications such as vertebroplasty (stabilization of a fractured vertebra with bone cement) using a syringe. A 2-wt % addition of sodium or potassium citrate with PC significantly improved cement injectability, decreased cement setting times from over 2 h to below 25 min, while increasing the compressive strength to a maximum of 125 MPa. Zeta-potential measurements indicated that the citrate anion was binding to one or more of the positively charged species causing charged repulsion between cement particles which dispersed aggregates and caused the liquefying effect of the anion. Analysis of the hydrating phases of PC indicated that the early strength producing PC phase (ettringite) developed within the first 2 h of setting following addition of the citrate anion, while this did not occur in the control cement (PC only). Within 24 h ettringite developed in PC as well as calcium-silicate-hydrate (C-S-H), the major setting phase of PC, whereas cements containing citrate did not develop this phase. The evidence suggested that in the presence of citrate the cements limited water supply appeared to be utilized for ettringite formation, producing the early strength of the citrate cements. The present study has demonstrated that it is possible to modify PC with citrate to both improve the injectability and crucially reduce the setting times of PC while improving the strength of the cement. PMID:24711245

  10. Effect of Initial Backfill Temperature on the Deformation Behavior of Early Age Cemented Paste Backfill That Contains Sodium Silicate

    Directory of Open Access Journals (Sweden)

    Aixiang Wu

    2016-01-01

    Full Text Available Enhancing the knowledge on the deformation behavior of cemented paste backfill (CPB in terms of stress-strain relations and modulus of elasticity is significant for economic and safety reasons. In this paper, the effect of the initial backfill temperature on the CPB’s stress-strain behavior and modulus of elasticity is investigated. Results show that the stress-strain relationship and the modulus of elasticity behavior of CPB are significantly affected by the curing time and initial temperature of CPB. Additionally, the relationship between the modulus of elasticity and unconfined compressive strength (UCS and the degree of hydration was evaluated and discussed. The increase of UCS and hydration degree leads to an increase in the modulus of elasticity, which is not significantly affected by the initial temperature.

  11. MODIFICATION OF PRECIPITATED CALCIUM CARBONATE FILLER USING SODIUM SILICATE/ZINC CHLORIDE BASED MODIFIERS TO IMPROVE ACID-RESISTANCE AND USE OF THE MODIFIED FILLER IN PAPERMAKING

    Directory of Open Access Journals (Sweden)

    Jing Shen

    2009-11-01

    Full Text Available In order to improve the acid-resistant property of papermaking grade precipitated calcium carbonate filler and to obtain modified filler in powder form, sodium silicate/zinc chloride based modifiers were used in filler modification, and the use of modified filler in papermaking of deinked pulp derived from recycled newspaper was also preliminarily investigated. Under the preliminarily optimized experimental conditions, when sodium silicate, zinc chloride, sodium hexametaphosphate, and phosphoric acid with dosages of 10 wt%, 3 wt%, 1 wt% and 0.2 wt%, respectively, were used as modifiers, and when the temperature, aging time, and PCC concentration during the filler modification process was 70 oC, 7 h and 9.1 wt%, respectively, the acid-resistant property of filler was significantly improved after modification, as evaluated using alum consumption and pH methods. The use of modified precipitated calcium carbonate filler prepared under the optimized conditions provided considerably more brightness and light scattering improvement in comparison to unmodified filler, and filler modification was found to have only negligible influence on tensile and burst strength of the paper, air permeability of the paper, and retention performance of the filler. Surface analysis of the modified filler using XPS and SEM confirmed the occurring of surface encapsulation and modification of precipitated calcium carbonate filler when the relevant modifiers were used in filler modification. The encapsulating effect of modifiers on filler was thought to be favorable to improvement in acid-resistant property, and optical properties of the filled paper.

  12. Development of Portland cement for orthopedic applications, establishing injectability and decreasing setting times.

    Science.gov (United States)

    Wynn-Jones, Gareth; Shelton, Richard M; Hofmann, Michael P

    2012-11-01

    The injectability of Portland cement (PC) with calcium chloride and calcium nitrate additives was investigated using a syringe with a 2 mm aperture for potential clinical applications such as vertebroplasty. Addition of either additive at 10 wt % increased the quantity of cement extruded through the syringe from approximately 25 wt % for the PC standard, to over 95 wt %. 10 wt % additions of either additive also decreased setting times from over 2 h to below 25 min. The compressive strength of the modified cements was all greater than the compressive strength of a human vertebral body. Decreasing either additive to 5 wt % generated compressive strengths after 24 h setting equal to polymethylmethacrylate, the cement used for the majority of vertebroplasty procedures. An initial early exotherm in the chloride cements was coupled with an X-ray diffraction (XRD) peak that indicated the early formation of the ettringite cement phase. In contrast, Fourier transform infrared (FTIR) spectroscopy and XRD data indicated that calcium nitrate may have stimulated early calcium silicate hydrate (C-S-H) production (the main strength producing phase of PC). Combining the two additives produced a synergistic effect with cements having increased injectabilities and compressive strengths compared with either addition used individually. This study has demonstrated that by modifying PC with nonproprietary chemicals it was possible to significantly increase cement injectability and reduce setting times whilst maintaining compressive strengths, making PC suitable for potential orthopedic applications. PMID:22887643

  13. ADVANCED CEMENTS FOR GEOTHERMAL WELLS

    Energy Technology Data Exchange (ETDEWEB)

    SUGAMA,T.

    2007-01-01

    Using the conventional well cements consisting of the calcium silicate hydrates (CaO-SiO{sub 2}-H{sub 2}O system) and calcium aluminum silicate hydrates (CaO-Al{sub 2}O{sub 3}-SiO{sub 2}-H{sub 2}O system) for the integrity of geothermal wells, the serious concern confronting the cementing industries was their poor performance in mechanically supporting the metallic well casing pipes and in mitigating the pipe's corrosion in very harsh geothermal reservoirs. These difficulties are particularly acute in two geological regions: One is the deep hot downhole area ({approx} 1700 m depth at temperatures of {approx} 320 C) that contains hyper saline water with high concentrations of CO{sub 2} (> 40,000 ppm) in conjunction with {approx} 100 ppm H{sub 2}S at a mild acid of pH {approx} 5.0; the other is the upper well region between the well's surface and {approx} 1000 m depth at temperatures up to 200 C. The specific environment of the latter region is characterized by highly concentrated H{sub 2}SO{sub 4} (pH < 1.5) brine containing at least 5000 ppm CO{sub 2}. When these conventional cements are emplaced in these harsh environments, their major shortcoming is their susceptibility to reactions with hot CO{sub 2} and H{sub 2}SO4, thereby causing their deterioration brought about by CO{sub 2}-catalyzed carbonation and acid-initiated erosion. Such degradation not only reduced rapidly the strength of cements, lowering the mechanical support of casing pipes, but also increased the extent of permeability of the brine through the cement layer, promoting the rate of the pipe's corrosion. Severely carbonated and acid eroded cements often impaired the integrity of a well in less than one year; in the worst cases, casings have collapsed within three months, leading to the need for costly and time-consuming repairs or redrilling operations. These were the reasons why the geothermal well drilling and cementing industries were concerned about using conventional well

  14. Processing and characterisation of calcium sulphoaluminate (CSA) eco-cements with tailored performances

    OpenAIRE

    García-Maté, Marta

    2014-01-01

    Climate change mitigation usually involves the reduction of greenhouse gases emissions, such as carbon dioxide (CO2). Every tonne of Ordinary Portland Cement (OPC) produces about one tonne of CO2. Consequently, OPC accounts for 5-6% of anthropogenic CO2 emissions and for 4% of total global warming. Due to these environmental problems the industry of building materials is under increasing pressure to reduce the energy used in the production of OPC and the greenhouse gas emissions. Hence, t...

  15. The effect of fly ash and coconut fibre ash as cement replacement materials on cement paste strength

    Science.gov (United States)

    Bayuaji, R.; Kurniawan, R. W.; Yasin, A. K.; Fatoni, H. AT; Lutfi, F. M. A.

    2016-04-01

    Concrete is the backbone material in the construction field. The main concept of the concrete material is composed of a binder and filler. Cement, concrete main binder highlighted by environmentalists as one of the industry are not environmentally friendly because of the burning of cement raw materials in the kiln requires energy up to a temperature of 1450° C and the output air waste CO2. On the other hand, the compound content of cement that can be utilized in innovation is Calcium Hydroxide (CaOH), this compound will react with pozzolan material and produces additional strength and durability of concrete, Calcium Silicate Hydrates (CSH). The objective of this research is to explore coconut fibers ash and fly ash. This material was used as cement replacement materials on cement paste. Experimental method was used in this study. SNI-03-1974-1990 is standard used to clarify the compressive strength of cement paste at the age of 7 days. The result of this study that the optimum composition of coconut fiber ash and fly ash to substitute 30% of cement with 25% and 5% for coconut fibers ash and fly ash with similar strength if to be compared normal cement paste.

  16. Antagonist effects of calcium on borosilicate glass alteration

    Energy Technology Data Exchange (ETDEWEB)

    Mercado-Depierre, S. [CEA Marcoule, DTCD SPDE LCLT, 30207 Bagnols sur Cèze (France); Angeli, F., E-mail: frederic.angeli@cea.fr [CEA Marcoule, DTCD SPDE LCLT, 30207 Bagnols sur Cèze (France); Frizon, F. [CEA Marcoule, DTCD SECM LP2C, 30207 Bagnols sur Cèze (France); Gin, S. [CEA Marcoule, DTCD SPDE LCLT, 30207 Bagnols sur Cèze (France)

    2013-10-15

    Graphical abstract: Display Omitted -- Highlights: •Kinetic study of glass alteration is investigated in calcium-enriched solutions. •New insights into silicon–calcium interactions in glass/cement systems are proposed. •Glass alteration is controlled by pH, Ca concentration and reaction progress. •Evidence of antagonist effects according to the importance of these parameters. -- Abstract: Numerous studies have been conducted on glass and cement durability in contact with water, but very little work to date has focused directly on interactions between the two materials. These interactions are mostly controlled by silicon–calcium reactivity. However, the physical and chemical processes involved remain insufficiently understood to predict the evolution of coupled glass–cement systems used in several industrial applications. Results are reported from borosilicate glass alteration in calcium-rich solutions. Our data show that four distinct behaviors can be expected according to the relative importance of three key parameters: the pH, the reaction progress (short- or long-term alteration) and the calcium concentration. Glass alteration is thus controlled by specific mechanisms depending on the solution chemistry: calcium complexation at the glass surface, precipitation of calcium silicate hydrates (C–S–H) or calcium incorporation in the altered layer. These findings highlight the impact of silicon–calcium interactions on glass durability and open the way for a better understanding of glass–cement mixing in civil engineering applications as well as in nuclear waste storage.

  17. Neutron Scattering Studies of Cement

    Science.gov (United States)

    Allen, Andrew

    2010-03-01

    Despite more than a century of research, basic questions remain regarding both the internal structure and the role of water in Ordinary Portland cement (OPC) concrete, the world's most widely used manufactured material. Most such questions concern the primary hydration product and strength-building phase of OPC paste, the calcium silicate hydrate (C-S-H) gel. When cement and water are mixed, this phase precipitates as clusters of nanoscale (nearly amorphous) colloidal particles with an associated water-filled inter-particle pore system. Most attempts to characterize the C-S-H gel and the behavior of the associated water involve drying or other processes that, themselves, change the bound water content within and around the gel. Neutron scattering methods do not suffer from this disadvantage. Furthermore, the neutron isotope effect and the neutron's sensitivity to molecular motion have enabled considerable progress to be made in recent years by: (i) determining the C-S-H composition, density and gel structure in small-angle neutron scattering (SANS) H/D contrast variation studies; (ii) elucidating the changing state of water within cement as hydration progresses using quasielastic neutron scattering (QENS); and (iii) measuring the production and consumption of nanoscale calcium hydroxide (CH), a by-product of cement hydration that co-exists with the C-S-H gel, using inelastic neutron scattering (INS). These experiments have provided new insights into the physics and chemistry of cement hydration, and have implications for the design of new concretes with pozzolanic cement additions that are intended to address environmental concerns and sustainability issues.

  18. In-situ Mechanical Manipulation of Wellbore Cements as a Solution to Leaky Wells

    Science.gov (United States)

    Kupresan, D.; Radonjic, M.; Heathman, J.

    2013-12-01

    Wellbore cement provides casing support, zonal isolation, and casing protection from corrosive fluids, which are essential for wellbore integrity. Cements can undergo one or more forms of failure such as debonding at cement/formation and cement/casing interface, fracturing and defects within cement matrix. Failures and defects within cement will ultimately lead to fluids migration, resulting in inter-zonal fluid migration and premature well abandonment. There are over 27,000 abandoned oil and gas wells only in The Gulf of Mexico (some of them dating from the late 1940s) with no gas leakage monitoring. Cement degradation linked with carbon sequestration can potentially lead to contamination of fresh water aquifers with CO2. Gas leaks can particularly be observed in deviated wells used for hydraulic fracking (60% leakage rate as they age) as high pressure fracturing increases the potential for migration pathways. Experimental method utilized in this study enables formation of impermeable seals at interfaces present in a wellbore by mechanically manipulating wellbore cement. Preliminary measurements obtained in bench scale experiments demonstrate that an impermeable cement/formation and cement/casing interface can be obtained. In post-modified cement, nitrogen gas flow-through experiments showed complete zonal isolation and no permeability in samples with pre-engineered microannulus. Material characterization experiments of modified cement revealed altered microstructural properties of cement as well as changes in mineralogical composition. Calcium-silicate-hydrate (CSH), the dominant mineral in hydrated cement which provides low permeability of cement, was modified as a result of cement pore water displacement, resulting in more dense structures. Calcium hydroxide (CH), which is associated with low resistance of cement to acidic fluids and therefore detrimental in most wellbore cements, was almost completely displaced and/or integrated in CSH as a result of

  19. Effect of calcium hydroxide on the bond strength of two bioactive cements and SEM evaluation of failure patterns.

    Science.gov (United States)

    Centenaro, Carolina Fabiana; Santini, Manuela Favarin; da Rosa, Ricardo Abreu; Nascimento, Angela Longo do; Kuga, Milton Carlos; Pereira, Jefferson Ricardo; Só, Marcus Vinícius Reis

    2016-05-01

    The aim of this study was to assess the effect of calcium hydroxide on bond strength of two bioactive cements. One-mm thick longitudinal slabs of root dentin were obtained from freshly extracted human monorradicular teeth (n = 60). Simulated root perforations (1 mm in diameter) were prepared in radicular dentin. Thereafter, the specimens were randomly divided into two groups (n = 30), according to the repair material: MTA (n = 30) and Biodentine (BD) (n = 30). Next, the specimens in each group were further randomly divided into 4 equal subgroups (n = 15) according to the prior use of Ca(OH)2: MTA/Ca(OH)2 and BD/Ca(OH)2 groups: perforations were filled with calcium hydroxide [Ca(OH)2] and after 7 days, it was removed, and MTA and BD groups: calcium hydroxide dressing were not used. Push-out test was performed at a crosshead speed of 1 mm/min. Bond strength values were compared statistically using Kruskal-Wallis test and Dunn's post-test at a significance level of 5%. The failure analysis was performed using a stereoscopic and classified as adhesive, cohesive and mixed. The push-out bond strength of MTA and BD was not affected by the prior use of Ca(OH)2 (p > 0.05). BD yielded higher push-out bond strength values compared with those of MTA, regardless of the use of Ca(OH)2 (p groups. Ca(OH)2 placement for perforations sealing does not alter the bond strength of MTA and BD to the root dentin. BD presented higher bond strength values than MTA. SCANNING 38:240-244, 2016. © 2015 Wiley Periodicals, Inc. PMID:26331376

  20. Stabilization of ZnCl2-containing wastes using calcium sulfoaluminate cement: leaching behaviour of the solidified waste form, mechanisms of zinc retention.

    Science.gov (United States)

    Berger, Stéphane; Cau Dit Coumes, Céline; Champenois, Jean-Baptiste; Douillard, Thierry; Le Bescop, Patrick; Aouad, Georges; Damidot, Denis

    2011-10-30

    To assess the potential of calcium sulfoaluminate cement to solidify and stabilize wastes containing high amounts of soluble zinc chloride (a strong inhibitor of Portland cement hydration), a simulated cemented waste form was submitted to leaching by pure water at a fixed pH of 7 for three months, according to a test designed to understand the degradation processes of cement pastes. Leaching was controlled by diffusion. The zinc concentration in the leachates always remained below the detection limit (2 μmol/L), showing the excellent confining properties of the cement matrix. At the end of the experiment, the solid sample exhibited three zones which were accurately characterized: (i) a highly porous and friable surface layer, (ii) a less porous intermediate zone in which several precipitation and dissolution fronts occurred, and (iii) the sound core. Ettringite was a good tracer for degradation. The good retention of zinc by the cement matrix was mainly attributed to the precipitation of a hydrated and well crystallized phase with platelet morphology (which may belong to the layered double hydroxide family) at early age (≤ 1 day), and to chemisorption onto aluminum hydroxide at later age. PMID:21889842

  1. Leaching of a simulated ZnCl2-rich radwaste stabilized with calcium sulfo-aluminate cement: experimental investigation and first attempt of modelling

    International Nuclear Information System (INIS)

    This paper reports the first leaching experiments performed on a simulated ZnCl2-rich waste stabilized with calcium sulfo-aluminate cement according to a standard test developed to understand and model the degradation processes of the cement paste. A simulated cemented waste form (cement paste prepared with a binder containing 20% gypsum and a 0.5 mol/L ZnCl2 mixing solution, and submitted to a thermal cycle at early age simulating the temperature rise and fall occurring in a 200 L drum of cemented waste) was submitted to leaching by pure water (fixed pH of 7) for 3 months. The cumulative quantities of Ca2+, OH-, Cl- and SO42- ions in the leachates increased linearly versus the square root of time, showing that leaching was controlled by diffusion. Zinc was never detected, showing the excellent confining properties of the cement matrix. Examination of the solid sample at the end of the experiment revealed three zones: (i) the highly porous and friable surface layer, composed of aluminum hydroxide, perovskite and probably C-(A)-S-H (thickness: 700 μm), (ii) a less porous intermediate zone in which several precipitation and dissolution fronts occurred (thickness: 1800 μm), and (iii) the sound core. The hydrated phase evolution along depth was qualitatively reproduced with a model coupling transport by diffusion and chemical reactions. (authors)

  2. The mechanical and biological studies of calcium phosphate cement-fibrin glue for bone reconstruction of rabbit femoral defects

    Directory of Open Access Journals (Sweden)

    Dong J

    2013-03-01

    Full Text Available Jingjing Dong,1,* Geng Cui,2,* Long Bi,1,* Jie Li,3 Wei Lei11Institute of Orthopedics, Xijing Hospital, Fourth Military Medical University, Xi’an, Shaanxi, People’s Republic of China; 2Institute of Orthopedics, General Hospital of PLA, Beijing, People’s Republic of China; 3Institute of Gynecology and Obstetrics, General Hospital of PLA, Beijing, People’s Republic of China*These authors contributed equally to this workAbstract: In order to improve the mechanical and biological properties of calcium phosphate cement (CPC, nanometer-biomaterial for bone reconstruction in the rabbit femoral defect model, fibrin glue (FG, the natural product, purified from the blood was introduced at three different ratios. The CPC powder and the FG solution were mixed, respectively, at the powder/liquid (P/L ratios (g/mL of 1:1, 3:1, and 5:1 (g/mL, and pure CPC was used as a control. After being implanted into the femoral defect in rabbit, the healing process was evaluated by micro-computed tomography scan, biomechanical testing, and histological examination. By micro-computed tomography analysis, the P/L ratio of 1:1 (g/mL group indicated the largest quantity of new bone formation at 4 weeks, 8 weeks, and 12 weeks after implantation, respectively. Bone volume per trabecular volume of the 1:1 group was highest in the four groups, which was 1.45% ± 0.42%, 7.35% ± 1.45%, and 29.10% ± 1.67% at 4 weeks, 8 weeks, and 12 weeks after the operation, respectively. In the biomechanical tests, the compressive strength and the elastic modulus of the three CPC–FG groups were much higher than those of the pure CPC group at the determined time point (P < 0.05. The histological evaluation also showed the best osseointegration in the 1:1 group at 4 weeks, 8 weeks, and 12 weeks after the operation, respectively. In the 1:1 group, the bone grew into the pore of the cement in the laminar arrangement and connected with the cement tightly at the 12th week after the operation

  3. PRINCIPLES OF RE-ENGINEERING METHODOLOGY FOR TECHNOLOGICAL PROCESS IN PROCESSING OF RAW MATERIAL COMPONENTS WHILE PRODUCING CEMENT AND SILICATE PRODUCTS

    Directory of Open Access Journals (Sweden)

    I. A. Busel

    2014-01-01

    necessity to modernize technological equipment used for grinding raw material components with the purpose to improve efficiency and quality, power- and resource saving. The possibility of using various grinding aids that permit to increase grinding productivity is shown in the paper. The paper studies an automation concept of the control system which used for grinding process of mineral raw material. A conceptual model for complexation of various methods grinding aids has been proposed in the paper. The paper presents methodological principles for simulation of technological process used for processing of mineral raw material while producing cement and silicate products. The parameters which are to be controlled and which are necessary for development of computer simulations of technological grinding process have been determined in the paper. The paper justifies an application of imitation simulation for creation of computer models. Methodology for imitation simulation of the technological process has been studied in the paper. The paper confirms the possibility to use analytical and probability methods. Imitation simulations of a grinding mill operation have been developed on the basis of experimental data and probability functions. The possibility of controlling technological process of raw material grinding has been demonstrated in the paper.While implementing the proposed complex of organizational and technical recommendations it is possible to increase grinding productivity up to 30-50 % and significantly reduce и существенно снизить energy consumption for mineral raw material grinding during production of cement and silicate products. The combined reengineering methodology for grinding process including all the mentioned intensification methods substantially increases quality of final products and reduces its self-cost that will favour its compatibility and attractiveness for consumers.

  4. Effect of Combined Calcium Hydroxide and Accelerated Portland Cement on Bone Formation and Soft Tissue Healing in Dog Bone Lesions

    Directory of Open Access Journals (Sweden)

    Khorshidi H

    2015-09-01

    Full Text Available Statement of Problem: Recent literatures show that accelerated Portland cement (APC and calcium hydroxide Ca (OH2 may have the potential to promote the bone regeneration. However, certain clinical studies reveal consistency of Ca (OH2, as one of the practical drawbacks of the material when used alone. To overcome such inconvenience, the combination of the Ca (OH2 with a bone replacement material could offer a convenient solution. Objectives: To evaluate the soft tissue healing and bone regeneration in the periodontal intrabony osseous defects using accelerated Portland cement (APC in combination with calcium hydroxide Ca (OH2, as a filling material. Materials and Methods: Five healthy adult mongrel dogs aged 2-3 years old (approximately 20 kg in weight with intact dentition and healthy periodontium were selected for this study. Two one-wall defects in both mesial and distal aspects of the 3rd premolars of both sides of the mandible were created. Therefore, four defects were prepared in each dog. Three defects in each dog were randomly filled with one of the following materials: APC alone, APC mixed with Ca (OH2, and Ca (OH2 alone. The fourth defect was left empty (control. Upon clinical examination of the sutured sites, the amount of dehiscence from the adjacent tooth was measured after two and eight weeks, using a periodontal probe mesiodistally. For histometric analysis, the degree of new bone formation was estimated at the end of the eighth postoperative week, by a differential point-counting method. The percentage of the defect volume occupied by new osteoid or trabecular bone was recorded. Results: Measurement of wound dehiscence during the second week revealed that all five APCs had an exposure of 1-2 mm and at the end of the study all samples showed 3-4 mm exposure across the surface of the graft material, whereas the Ca (OH2, control, and APC + Ca (OH2 groups did not show any exposure at the end of the eighth week of the study. The most

  5. Ceramic joining through reactive wetting of alumina with calcium aluminate refractory cements

    Indian Academy of Sciences (India)

    K Geetha; A M Umarji; T R N Kutty

    2000-08-01

    Compositions in CaO–Al2O3 system have been prepared by gel–to–crystallite conversion method. Reactive powders of 1 : 2, 1 : 1, 2 : 1 and 3 : 1 of CaO and Al2O3 compositions were obtained by calcining the product at 800–1200°C. Fine grained powders were used as refractory cement for joining alumina ceramics. An optimum temperature of 1450°C for 4 h produced joints of satisfactory strength. The microstructure and X-ray phase analysis of the fractured joint surface clearly indicate reactive wetting of the alumina ceramics. This wetting enhances the joining of alumina substrates and can be attributed to the formation of Ca12Al14O33 liquid phase. The results are explained by using CaO–Al2O3 phase diagram.

  6. Histological evaluation of direct pulp capping with novel nanostructural materials based on active silicate cements and Biodentine® on pulp tissue

    Directory of Open Access Journals (Sweden)

    Popović-Bajić Marijana

    2013-01-01

    Full Text Available The aim of this study was to examine the effect of Biodentine® and two new nanostructured materials based on active silicate cements on exposed tooth pulp of Vietnamese pigs. The study comprised 40 teeth in two Vietnamese pigs (24 months old. After class V cavity preparation, the pulp on each tooth was exposed using a small round bur. The following materials were applied on pulp exposures: Biodentine® (10 teeth, ALBO MPCA-I (10 teeth, and ALBO MPCA-II (10 teeth. In the control group, exposed pulp was covered with ProRoot MTA® (10 teeth. After the observation period of 28 days, the animals were sacrificed and the teeth prepared for histological analysis. Light microscope was used for the analysis of dentin bridge formation, tissue reorganization and inflammation, and the presence of bacteria in the pulp. In the group of Biodentine®, a complete dentin bridge was noted in 3 cases, while incomplete dentin bridge in the form of dental islets was detected in 4 cases. Nanostructured material ALBO-MPCA I provided complete dentin bridge formation in 5 teeth, in 3 teeth the formed dentin bridge was incomplete. ALBO MPCA-II showed complete closure of the pulp opening by dentin bridge in 4 samples, while in the same number of teeth it was incomplete. In the control group, 4 teeth showed a complete dentin bridge, whereas in 6 teeth it was incomplete. Histological analysis indicated favourable therapeutic effects of Biodentine® and the two materials ALBO-MPCA I and ALBO-MPCA II after teeth pulp capping in Vietnamese pigs. Pulp reaction was similar to that caused by ProRoot MTA®. [Projekat Ministarstva nauke Republike Srbije, br. ON172026

  7. EFFECT OF MgO ON THE COMPOSITION AND PROPERTIES OF BELITE-BARIUM CALCIUM SULPHOALUMINATE CEMENT IN THE PRESENCE OF Na2O AND K2O

    Directory of Open Access Journals (Sweden)

    Jie Zhang

    2015-06-01

    Full Text Available The purpose of this study is to explore the effect of MgO (1 - 9 wt. % on the composition and properties of belite-barium calcium sulphoaluminate cement with additions of Na2O and K2O. The results show that 1 - 5 wt. % content of MgO can stabilize crystal types of M3-C3S, R-C3S and β-C2S. Moreover, MgO can promote the formation of C3S and C4AF, but has little effect on the formation of C2.75B1.25A3$ and C3A. The C3A/C4AF ratio is reduced by 22 % at 5 wt. % MgO, which indicates that appropriate MgO can decrease the liquid viscosity. In the presence of Na2O and K2O, the highest limit of incorporated amount of MgO is about 3 wt. %, which is higher than that in Portland cement clinker of 2 wt. %. Besides, MgO favors the formation of small C3S crystals in size of 4 - 20 μm. MgO enhances the hydration rate and mechanical property of cement at an optimal dosage (1 - 5 wt. %, beyond which an adverse effect could be resulted. At a MgO dosage of 5 wt. %, the compressive strengths of the cement at 1, 3, 7 and 28 days are 15.8, 39.3, 68.6 and 97.3 MPa, which increases by 116 %, 17 %, 10 % and 6 % respectively compared to the cement without MgO dopant. This study could lead to the effective use of magnesia-rich limestone in industrial production of belite-barium calcium sulphoaluminate cement.

  8. Tunable luminescence and white light emission of novel multiphase sodium calcium silicate nanophosphors doped with Ce3+, Tb3+, and Mn2+ ions

    International Nuclear Information System (INIS)

    This study reports the sol–gel synthesis of sodium calcium multiphase silicate (SCMS) nanophosphors. X-ray powder diffraction indicated the crystallization of devitrite (Na2Ca3Si6O16), wollastonite-2M (CaSiO3), and cristobalite (SiO2) phases that consistently occurred together upon repeated syntheses. The multiphase silicate system was used as a host matrix for varied concentrations of Ce3+, Tb3+, and Mn2+ dopant ions which resulted in tunable photoluminescence. A broad violet/UV emission band of Ce3+ (350–425 nm) combined with blue-green emissions of Tb3+ (488 and 545 nm) and a yellow-orange emission of Mn2+ (560 nm) resulted in the observance of white light (x=0.31, y=0.32, TC=6624 K) under midwave UV excitation (300–340 nm). Energy transfer from Ce3+→Tb3+ and Ce3+→Mn2+ was confirmed by steady state and time-resolved emission spectra, lifetime, and quantum yield measurements. The structural properties, morphology, and elemental composition of the nanophosphors were characterized by Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS). -- Highlights: • White light-emitting multiphase silicate nanophosphors were prepared for the first time. • Multiple crystalline silicate phases were reproduced consistently by repeated syntheses. • Energy transfer from Ce3+→Tb3+ and Ce3+→Mn2+ was confirmed by PL, lifetime, and QY measurements

  9. Characterization of the calcium-fluoroaluminosilicate glass prepared by a non-hydrolytic sol-gel route for future dental application as glass ionomer cement

    OpenAIRE

    Alexandre Cestari; Lilian Rodrigues Avila; Evelisy Cristina de Oliveira Nassor; Paula Fabiana dos Santos Pereira; Paulo Sergio Calefi; Katia Jorge Ciuffi; Shirley Nakagaki; Antonio Carlos Pereira Gomes; Eduardo Jose Nassar

    2009-01-01

    Glass ionomer cements are widely employed in dentistry due to their physical, biological and mainly anti-caries properties. Glass ionomers consist of an aluminosilicate glass matrix modified with other elements, and they contain large quantities of fluorine. In this study, we report on the preparation of calcium-fluoroaluminosilicate glasses by a nonhydrolytic sol-gel route as an alternative approach to obtaining alumina-silica matrices. The glass powders were prepared via the non-hydrolytic ...

  10. Do cement nanoparticles exist in space ?

    CERN Document Server

    Bilalbegovic, G; Mohacek-Grosev, V

    2014-01-01

    The calcium-silicate-hydrate is used to model properties of cement on Earth. We study cementitious nanoparticles and propose these structures as components of cosmic dust grains. Quantum density functional theory methods are applied for the calculation of infrared spectra of Ca4Si4O14H4, Ca6Si3O13H2, and Ca12Si6O26H4 clusters. We find bands distributed over the near, mid and far-infrared region. A specific calcium-silicate-hydrate spectral feature at 14 microns, together with the bands at 10 and 18 microns which exist for other silicates as well, could be used for a detection of cosmic cement. We compare calculated bands with the 14 microns features in the spectra of HD 45677, HD 44179, and IRC+10420 which were observed by Infrared Space Observatory and classified as remaining. High abundance of oxygen atoms in cementitious nanoparticles could partially explain observed depletion of this element from the interstellar medium into dust grains.

  11. Recovery of phosphorus from wastewater by calcium silicate hydrate%水化硅酸钙回收污水中磷的试验研究

    Institute of Scientific and Technical Information of China (English)

    王鑫永; 陈雪初; 何圣兵; 李春杰; 孔海南; 李思劫

    2011-01-01

    Taking simulation wastewater as the research object, a test on phosphorus removal from waste-water by synthesized calcium silicate hydrate was carried out, and the influences of contact time, Ca2+ concentration, initial pH value, interfering ion and some other factors on phosphorus removal were investigated. The results of the test on phosphorus recovery from actual wastewater by calcium silicate hydrate showed that, after 8 hours of reaction, the amount of phosphorus recovery reached 101 mg/g; the phosphorus content of the wastewater, converted into P2O5, was larger then that of the common water-soluble phosphate fertilizer: calcium superphosphate; furthermore, phosphorus was released rapidly after the product had been treated by acid, and the release rate was nearly 100% within 1 hour, which indicated that, the said material could enrich and reclaim phosphorus from actual wastewater, and would have good application prospect.%采用合成水化硅酸钙进行污水除磷试验,以模拟污水为研究对象,考察了接触时间、Ca2+浓度、初始pH值、干扰离子等因素对除磷效果的影响,在利用水化硅酸钙回收实际污水中磷的试验发现,在处理8h后除磷量达到101 mg/g,折合P2O5含量超过常用的水溶性磷肥过磷酸钙,且产物经酸处理后将快速释磷,在1h后磷释放率接近100%,显示该材料能富集回收实际污水中的磷,具有较好的应用前景.

  12. Effect of Tartaric Acid on Hydration of a Sodium-Metasilicate-Activated Blend of Calcium Aluminate Cement and Fly Ash F

    Directory of Open Access Journals (Sweden)

    Tatiana Pyatina

    2016-05-01

    Full Text Available An alkali-activated blend of aluminum cement and class F fly ash is an attractive solution for geothermal wells where cement is exposed to significant thermal shocks and aggressive environments. Set-control additives enable the safe cement placement in a well but may compromise its mechanical properties. This work evaluates the effect of a tartaric-acid set retarder on phase composition, microstructure, and strength development of a sodium-metasilicate-activated calcium aluminate/fly ash class F blend after curing at 85 °C, 200 °C or 300 °C. The hardened materials were characterized with X-ray diffraction, thermogravimetric analysis, X-ray computed tomography, and combined scanning electron microscopy/energy-dispersive X-ray spectroscopy and tested for mechanical strength. With increasing temperature, a higher number of phase transitions in non-retarded specimens was found as a result of fast cement hydration. The differences in the phase compositions were also attributed to tartaric acid interactions with metal ions released by the blend in retarded samples. The retarded samples showed higher total porosity but reduced percentage of large pores (above 500 µm and greater compressive strength after 300 °C curing. Mechanical properties of the set cements were not compromised by the retarder.

  13. Calcium-magnesium carbonate solid solutions from Holocene conglomerate cements and travertines in the Coast Range of California

    Science.gov (United States)

    Barnes, I.; O'Neil, J.R.

    1971-01-01

    Two calcium-magnesium carbonate solid solutions form Holocene travertines and conglomerate cements in fresh water stream channels of the Coast Range of California. Calcite does not yield the {015} diffraction maximum. The {006} diffraction maximum is lacking over most of the range of composition of calcite. Calcite has compositions from CaCO3 to Ca0.5Mg0.5CO3. Dolomite yields both the {006} and {015} diffraction maxima over its entire composition range, Ca0.6Mg0.4CO3 to Ca0.5Mg0.5CO3. The Ca-Mg carbonates form in isotopic equilibrium and thermodynamic disequilibrium from dispersion of Ca2+-rich water into CO32--rich water within the alluvium. The stable isotope data suggest that all the Mg-rich carbonates are primary precipitates and not a result of Mg-substitution in precursor CaCO3. There is a correlation between ??C13 and Mg content of the carbonates which predicts a 5%. fractionation of C13 between dolomite and calcite at sedimentary temperatures. C14 is incorporated in Ca-Mg carbonates forming from C13-poor meteoric waters and C13-rich waters from Cretaceous sediments. C14 ages of the Ca-Mg carbonates are apparent, and cannot be corrected to absolute values. Solution rates of calcite decrease with increasing MgCO3 content; dolomite dissolves slower than any calcite. ?? 1971.

  14. Calcium enriched mixture cement for primary molars exhibiting root perforations and extensive root resorption: report of three cases.

    Science.gov (United States)

    Tavassoli-Hojjati, Sara; Kameli, Somayeh; Rahimian-Emam, Sara; Ahmadyar, Maryam; Asgary, Saeed

    2014-01-01

    In primary molars with root perforations of endodontic origin, tooth extraction and space maintainer are recommended. Calcium-enriched mixture (CEM) cement is a new biomaterial demonstrating favorable sealability/biocompatibility. This report presents a novel treatment modality for cases of primary molar teeth with root perforations associated with a periodontal lesion due to extensive inflammatory root resorption, whereby CEM was used as a perforation repair/pulpotomy biomaterial. Three cases of primary molar root perforations due to inflammatory resorption were selected; all cases were associated with furcal lesions of endodontic origin. Pulp chambers were accessed/irrigated with NaOCl; the root canal orifices were filled with CEM and restored with stainless steel crowns. Clinical/radiographic examinations up to 17 months revealed that all teeth were functional and free of signs/symptoms of infection and all had complete bone healing. Further trials are suggested to confirm CEM use for management of root perforations in primary molars exhibiting root perforation. PMID:24717704

  15. Whisker-reinforced bioactive composites containing calcium phosphate cement fillers: effects of filler ratio and surface treatments on mechanical properties.

    Science.gov (United States)

    Xu, H H; Quinn, J B

    2001-11-01

    Calcium phosphate cement (CPC) sets to form microporous solid hydroxyapatite with excellent osteoconductivity, but its brittleness and low strength prohibit use in stress-bearing locations. The aim of this study was to incorporate prehardened CPC particles and ceramic whiskers in a resin matrix to improve the strength and fracture resistance, and to investigate the effects of key microstructural variables on composite mechanical properties. Two types of whiskers were used: silicon nitride, and silicon carbide. The whiskers were surface-treated by fusing with silica and by silanization. The CPC particle fillers were either silanized or not silanized. Seven mass ratios of whisker-silica/CPC were mixed: 0:1 (no whisker-silica), 1:5, 1:2, 1:1, 2:1, 5:1, and 1:0 (no CPC). Each powder was blended with a bisphenol-a-glycidyl methacrylate-based resin to harden in 2 x 2 x 25 mm molds by two-part chemical curing. The specimens were tested in three-point flexure to measure strength, work-of-fracture (toughness), and elastic modulus. Two-way analysis of variance was used to analyze the data, and scanning electron microscopy was used to examine specimen fracture surfaces. The whisker-silica/CPC ratio had significant effects on composite properties (p particles without whiskers. The composite properties were determined by whisker-to-CPC ratio and filler surface treatments. PMID:11484178

  16. CaO-based pellets supported by calcium aluminate cements for high-temperature CO2 capture.

    Science.gov (United States)

    Manovic, Vasilije; Anthony, Edward J

    2009-09-15

    The development of highly efficient CaO-based pellet sorbents, using inexpensive raw materials (limestones) or the spent sorbent from CO2 capture cycles, and commercially available calcium aluminate cements (CA-14, CA-25, Secar 51, and Secar 80), is described here. The pellets were prepared using untreated powdered limestones or their corresponding hydrated limes and were tested for their CO2 capture carrying capacities for 30 carbonation/calcination cycles in a thermogravimetric analyzer (TGA). Their morphology was also investigated by scanning electron microscopy (SEM) and their compositions before and after carbonation/calcination cycleswere determined by X-ray diffraction (XRD). Pellets prepared in this manner showed superior behavior during CO2 capture cycles compared to natural sorbents, with the highest conversions being > 50% after 30 cycles. This improved performance was attributed to the resulting substructure of the sorbent particles, i.e., a porous structure with nanoparticles incorporated. During carbonation/calcination cycles mayenite (Ca12Al14O33) was formed, which is believed to be responsible for the favorable performance of synthetic CaO-based sorbents doped with alumina compounds. An added advantage of the pellets produced here is their superior strength, offering the possibility of using them in fluidized bed combustion (FBC) systems with minimal sorbent loss due to attrition. PMID:19806751

  17. Different Angiogenic Abilities of Self-Setting Calcium Phosphate Cement Scaffolds Consisting of Different Proportions of Fibrin Glue

    Directory of Open Access Journals (Sweden)

    Jintao Xiu

    2014-01-01

    Full Text Available To investigate the different angiogenic abilities of the self-setting calcium phosphate cement (CPC consisting of different proportions of fibrin glue (FG, the CPC powder and the FG solution were mixed at the powder/liquid (P/L ratios of 1 : 0.5, 1 : 1, and 1 : 2 (g/mL, respectively, and pure CPC was used as a control. After being implanted into the lumbar dorsal fascia of the rabbit, the angiogenic process was evaluated by histological examination and CD31 immunohistochemistry to detect the new blood vessels. The result of the new blood vessel showed that the P/L ratio of 1 : 1 group indicated the largest quantity of new blood vessel at 4 weeks, 8 weeks, and 12 weeks after implantation, respectively. The histological evaluation also showed the best vascular morphology in the 1 : 1 group at 4 weeks, 8 weeks, and 12 weeks after the operation, respectively. Our study indicated that the CPC-FG composite scaffold at the P/L ratio of 1 : 1  (g/mL stimulated angiopoiesis better than any other P/L ratios and has significant potential as the bioactive material for the treatment of bone defects.

  18. Enhanced healing of rabbit segmental radius defects with surface-coated calcium phosphate cement/bone morphogenetic protein-2 scaffolds

    International Nuclear Information System (INIS)

    Large osseous defects remain a difficult clinical problem in orthopedic surgery owing to the limited effective therapeutic options, and bone morphogenetic protein-2 (BMP-2) is useful for its potent osteoinductive properties in bone regeneration. Here we build a strategy to achieve prolonged duration time and help inducting new bone formation by using water-soluble polymers as a protective film. In this study, calcium phosphate cement (CPC) scaffolds were prepared as the matrix and combined with sodium carboxymethyl cellulose (CMC-Na), hydroxypropylmethyl cellulose (HPMC), and polyvinyl alcohol (PVA) respectively to protect from the digestion of rhBMP-2. After being implanted in the mouse thigh muscles, the surface-modified composite scaffolds evidently induced ectopic bone formation. In addition, we further evaluated the in vivo effects of surface-modified scaffolds in a rabbit radius critical defect by radiography, three dimensional micro-computed tomographic (μCT) imaging, synchrotron radiation-based micro-computed tomographic (SRμCT) imaging, histological analysis, and biomechanical measurement. The HPMC-modified CPC scaffold was regarded as the best combination for segmental bone regeneration in rabbit radius. - Highlights: • A simple surface-coating method was used to fabricate composite scaffolds. • Growth factor was protected from rapid depletion via superficial coating. • Significant promotion of bone regeneration was achieved. • HPMC-modification displayed optimal effect of bone regeneration

  19. In vitro study of using calcium phosphate cement as immunoisolative device to enclose insulinoma/agarose microspheres as bioartificial pancreas.

    Science.gov (United States)

    Kai-Chiang, Yang; Ching-Yao, Yang; Chang-Chin, Wu; Tzong-Fu, Kuo; Feng-Huei, Lin

    2007-12-15

    In this study, the feasibility of using calcium phosphate cement (CPC) as immunoisolative device to enclose insulinoma/agarose microspheres as bioartificial pancreas was evaluated. We fabricated a chamber by CPC and utilized X-ray diffraction, Scanning electron microscope and Mercury intrusion porosimetry to identify the characters of the CPC chamber. The nominal molecular weight cut-off and cytotoxicity of CPC chamber were also evaluated. An insulinoma cell line (RIN-m5F) was chosen as insulin source and encapsulated in agarose microspheres and then enclosed in preformed CPC chamber. Insulin secretion was analyzed by Enzyme-linked immunosorbant assay to evaluate the function of insulinoma enclosed in CPC chamber. Results showed that the CPC chamber was non-cytotoxicity to insulinoma and can block the penetration of molecules which molecular weight larger than 12.4 kDa. Insulinoma inside the CPC chamber can secrete insulin in stable level for 30 days. This study indicated that we may use CPC as immunoisolative material to enclose insulinoma/agarose microspheres as bioartificial pancreas. PMID:17514757

  20. Enhanced healing of rabbit segmental radius defects with surface-coated calcium phosphate cement/bone morphogenetic protein-2 scaffolds

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Yi; Hou, Juan; Yin, ManLi [Engineering Research Center for Biomedical Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237 (China); Wang, Jing, E-mail: biomatwj@163.com [Engineering Research Center for Biomedical Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237 (China); Liu, ChangSheng, E-mail: csliu@sh163.net [Engineering Research Center for Biomedical Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237 (China); The State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237 (China); Key Laboratory for Ultrafine Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237 (China)

    2014-11-01

    Large osseous defects remain a difficult clinical problem in orthopedic surgery owing to the limited effective therapeutic options, and bone morphogenetic protein-2 (BMP-2) is useful for its potent osteoinductive properties in bone regeneration. Here we build a strategy to achieve prolonged duration time and help inducting new bone formation by using water-soluble polymers as a protective film. In this study, calcium phosphate cement (CPC) scaffolds were prepared as the matrix and combined with sodium carboxymethyl cellulose (CMC-Na), hydroxypropylmethyl cellulose (HPMC), and polyvinyl alcohol (PVA) respectively to protect from the digestion of rhBMP-2. After being implanted in the mouse thigh muscles, the surface-modified composite scaffolds evidently induced ectopic bone formation. In addition, we further evaluated the in vivo effects of surface-modified scaffolds in a rabbit radius critical defect by radiography, three dimensional micro-computed tomographic (μCT) imaging, synchrotron radiation-based micro-computed tomographic (SRμCT) imaging, histological analysis, and biomechanical measurement. The HPMC-modified CPC scaffold was regarded as the best combination for segmental bone regeneration in rabbit radius. - Highlights: • A simple surface-coating method was used to fabricate composite scaffolds. • Growth factor was protected from rapid depletion via superficial coating. • Significant promotion of bone regeneration was achieved. • HPMC-modification displayed optimal effect of bone regeneration.