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Sample records for calcium silicate hydrates

  1. 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.

  2. Novel understanding of calcium silicate hydrate from dilute hydration

    KAUST Repository

    Zhang, Lina

    2017-05-13

    The perspective of calcium silicate hydrate (C-S-H) is still confronting various debates due to its intrinsic complicated structure and properties after decades of studies. In this study, hydration at dilute suspension of w/s equaling to 10 was conducted for tricalcium silicate (C3S) to interpret long-term hydration process and investigate the formation, structure and properties of C-S-H. Based on results from XRD, IR, SEM, NMR and so forth, loose and dense clusters of C-S-H with analogous C/S ratio were obtained along with the corresponding chemical formulae proposed as Ca5Si4O13∙6.2H2O. Crystalline structure inside C-S-H was observed by TEM, which was allocated at the foil-like proportion as well as the edge of wrinkles of the product. The long-term hydration process of C3S in dilute suspension could be sketchily described as migration of calcium hydroxide and in-situ growth of C-S-H with equilibrium silicon in aqueous solution relatively constant and calcium varied.

  3. Calcium silicate hydrates: Solid and liquid phase composition

    OpenAIRE

    Lothenbach Barbara; Nonat André

    2015-01-01

    © 2015 Elsevier Ltd. 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 ...

  4. Molecular Dynamics Modeling of Hydrated Calcium-Silicate-Hydrate (CSH) Cement Molecular Structure

    Science.gov (United States)

    2014-08-30

    paste consisting of starting configuration of dry cement powder and water mixture by itself is a complex, multi-scale material system. Though...high pressure molecular structural behavior of the hydrated CSH. Portland cement in the powder form consists of four different major constituents...Tricalcium silicate (C3S), Di-Calcium silicate (C2S), Tri-Calcium aluminate (C3A), and Tetra calcium aluminoferrite (C4AF) [1]. Different mixture

  5. 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.

  6. 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.

  7. Hydration characteristics of calcium silicate cements with alternative radiopacifiers used as root-end filling materials.

    Science.gov (United States)

    Camilleri, Josette

    2010-03-01

    Mineral trioxide aggregate (MTA) is composed of calcium silicate cement and bismuth oxide added for radiopacity. The bismuth oxide in MTA has been reported to have a deleterious effect on the physical and chemical properties of the hydrated material. This study aimed to investigate the hydration mechanism of calcium silicate cement loaded with different radiopacifiers for use as a root-end filling material. Calcium silicate cement loaded with barium sulfate, gold, or silver/tin alloy was hydrated, and paste microstructure was assessed after 30 days. In addition, atomic ratio plots of Al/Ca versus Si/Ca and S/Ca and Al/Ca were drawn, and X-ray energy dispersive analysis of the hydration products was performed to assess for inclusion of heavy metals. The leachate produced from the cements after storage of the cements in water for 28 days and the leaching of the radiopacifiers in an alkaline solution was assessed by using inductively coupled plasma. The hydrated calcium silicate cement was composed of calcium silicate hydrate, calcium hydroxide, ettringite, and monosulfate. Unhydrated cement particles were few. No heavy metals were detected in the calcium silicate hydrate except for the bismuth in MTA. Calcium was leached out early in large quantities that reduced with time. The barium and bismuth were leached in increasing amounts. Copper was the most soluble in alkaline solution followed by bismuth and barium in smaller amounts. The bismuth oxide can be replaced by other radiopacifiers that do not affect the hydration mechanism of the resultant material. Copyright (c) 2010 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  8. NMR study of hydrated calcium silicates; Etude par RMN de la structure des silicates de calcium hydrates

    Energy Technology Data Exchange (ETDEWEB)

    Klur, I

    1996-02-26

    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.) 101 refs.

  9. Effect of Hydration and Confinement on Micro-Structure of Calcium-Silicate-Hydrate Gels

    Science.gov (United States)

    Gadde, Harish Kumar

    Calcium-silicate-hydrate(C-S-H) gel is a primary nano-crystalline phase present in hydrated Ordinary Portland Cement (OPC) responsible for its strength and creep behavior. Our reliance on cement for infrastructure is global, and there is a need to improve infrastructure life-times. A way forward is to engineer the cement with more durability and long-term strength. The main purpose of this research is to quantify the micro-structure of C-S-H to see if cement can be engineered at various length scales to improve long-term behavior by spatial arrangement. We investigate the micro-structure evolution of C-S-H in cement as a function of hydration time and confinement. Scanning electron microscopy (SEM) and Energy Dispersive X-ray Spectroscopy (EDS) were used to quantify the material and spatial properties of C-S-H as a function of hydration time. The data obtained from these experiments was used to identify C-S-H phases in cement sample. Pair Distribution Function (PDF) analysis of HD C-S-H phase with different hydration times was done at Advanced Photon Source, Argonne National Laboratory, beamline 11-ID-B. Only nonlinear trends in the atomic ordering of C-S-H gel as a function of hydration time were observed. Solid state 29Si Nuclear Magnetic Resonance (NMR) was used to quantify the effect of confinement on two types of C-S-H: white cement C-S-H and synthetic C-S-H. NMR spectra revealed that there is no significant difference in the structure of C-S-H due to confinement when compared with unconfined C-S-H. It is also found that there is significant difference in the Si environments of these two types of C-S-H. Though it does seem possible to engineer the cement on atomic scales, all these studies reveal that engineering cement on such a scale requires a more statistically accurate understanding of intricate structure of C-S-H than is currently available.

  10. Confined Water in Layered Silicates: The Origin of Anomalous Thermal Expansion Behavior in Calcium-Silicate-Hydrates.

    Science.gov (United States)

    Krishnan, N M Anoop; Wang, Bu; Falzone, Gabriel; Le Pape, Yann; Neithalath, Narayanan; Pilon, Laurent; Bauchy, Mathieu; Sant, Gaurav

    2016-12-28

    Water, under conditions of nanoscale confinement, exhibits anomalous dynamics, and enhanced thermal deformations, which may be further enhanced when such water is in contact with hydrophilic surfaces. Such heightened thermal deformations of water could control the volume stability of hydrated materials containing nanoconfined structural water. Understanding and predicting the thermal deformation coefficient (TDC, often referred to as the CTE, coefficient of thermal expansion), which represents volume changes induced in materials under conditions of changing temperature, is of critical importance for hydrated solids including: hydrogels, biological tissues, and calcium silicate hydrates, as changes in their volume can result in stress development, and cracking. By pioneering atomistic simulations, we examine the physical origin of thermal expansion in calcium-silicate-hydrates (C-S-H), the binding agent in concrete that is formed by the reaction of cement with water. We report that the TDC of C-S-H shows a sudden increase when the CaO/SiO2 (molar ratio; abbreviated as Ca/Si) exceeds 1.5. This anomalous behavior arises from a notable increase in the confinement of water contained in the C-S-H's nanostructure. We identify that confinement is dictated by the topology of the C-S-H's atomic network. Taken together, the results suggest that thermal deformations of hydrated silicates can be altered by inducing compositional changes, which in turn alter the atomic topology and the resultant volume stability of the solids.

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

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Na; Li, Hongxu [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Beijing Key Laboratory of Rare and Precious Metals Green Recycling and Extraction, University of Science and Technology Beijing, Beijing 100083 (China); Zhao, Yazhao [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Liu, Xiaoming, E-mail: liuxm@ustb.edu.cn [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Beijing Key Laboratory of Rare and Precious Metals Green Recycling and Extraction, University of Science and Technology Beijing, Beijing 100083 (China)

    2016-04-05

    Highlights: • Cementitious material was designed according to [SiO{sub 4}] polymerization degree of raw materials. • The cementitious material composed of calcium silicate slag yields excellent physical and mechanical properties. • Amorphous C–A–S–H gel and rod-like ettringite are predominantly responsible for the strength development. • Leaching toxicity and radioactivity tests show the cementitious material is environmentally acceptable. - Abstract: Calcium silicate slag is an alkali leaching waste generated during the process of extracting Al{sub 2}O{sub 3} 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){sub 2} with small amount of zeolite-like minerals such as CaAl{sub 2}Si{sub 2}O{sub 8}·4H{sub 2}O and Na{sub 2}Al{sub 2}Si{sub 2}O{sub 8}·H{sub 2}O. 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.

  12. Nanoscale Charge Balancing Mechanism in Alkali Substituted Calcium-Silicate-Hydrate Gels

    CERN Document Server

    Özçelik, V Ongun

    2016-01-01

    Alkali-activated materials and related alternative cementitious systems are sustainable material technologies that have the potential to substantially lower CO$_2$ emissions associated with the construction industry. However, the impact of augmenting the chemical composition of the material on the main binder phase, calcium-silicate-hydrate gel, is far from understood, particularly since this binder phase is disordered at the nanoscale. Here, we reveal the presence of a charge balancing mechanism at the molecular level, which leads to stable structures when alkalis (i.e., Na or K) are incorporated into a calcium-silicate-hydrate gel, as modeled using crystalline 14{\\AA} tobermorite. These alkali containing charge balanced structures possess superior mechanical properties compared to their charge unbalanced counterparts. Our results, which are based on first-principles simulations using density functional theory, include the impact of charge balancing on the optimized geometries of the new model phases, format...

  13. Effects of polymer intercalation in calcium silicate hydrates on drug loading capacities and drug release kinetics: an X-ray absorption near edge structure study

    National Research Council Canada - National Science Library

    Guo, Xiaoxuan; Zhu, Ying-Jie; Hu, Yongfeng; Wu, Jin; Yiu, Yun-Mui; Sham, Tsun-Kong

    2017-01-01

    Different calcium silicate hydrate (CSH)/polymer composites are synthesized by using a controlled precipitation reaction between calcium salt and silicate salt, followed by the addition of various polymer solutions at room temperature...

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

    OpenAIRE

    Suzuki, Hiroshi; Bae, Sungchul; Kanematsu, Manabu

    2016-01-01

    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. Th...

  15. Reactive molecular simulation on the calcium silicate hydrates/polyethylene glycol composites

    Science.gov (United States)

    Zhou, Yang; Hou, Dongshuai; Jiang, Jinyang; She, Wei; Yu, Jiao

    2017-11-01

    Calcium silicate hydrates (C-S-H) may potentially exhibit extraordinary performance when modified by polymers, in which way the properties of cement-based materials can be improved from the genetic level. In this molecular dynamics simulation of the interaction between C-S-H and polyethylene glycol, apart from the H bond network connection in the interface, another chemical adsorption was observed. Calcium of C-S-H broke the Csbnd O bond of PEG and formed a new Casbnd C connection, which created a stronger link between the organic and inorganic phases.

  16. Dynamical behaviors of structural, constrained and free water in calcium- and magnesium-silicate-hydrate gels.

    Science.gov (United States)

    Le, Peisi; Fratini, Emiliano; Ito, Kanae; Wang, Zhe; Mamontov, Eugene; Baglioni, Piero; Chen, Sow-Hsin

    2016-05-01

    The mechanical properties of cement pastes depend strongly on their porosities. In a saturated paste, the porosity links to the free water volume after hydration. Structural water, constrained water, and free water have different dynamical behavior. Hence, it should be possible to extract information on pore system by exploiting the water dynamics. We investigated the slow dynamics of hydration water confined in calcium- and magnesium-silicate-hydrate (C-S-H and M-S-H) gels using high-resolution quasi-elastic neutron scattering (QENS) technique. C-S-H and M-S-H are the chemical binders present in calcium rich and magnesium rich cements. We measured three M-S-H samples: pure M-S-H, M-S-H with aluminum-silicate nanotubes (ASN), and M-S-H with carboxyl group functionalized ASN (ASN-COOH). A C-S-H sample with the same water content (i.e. 0.3) is also studied for comparison. Structural water in the gels contributes to the elastic component of the QENS spectrum, while constrained water and free water contribute the quasi-elastic component. The quantitative analysis suggests that the three components vary for different samples and indicate the variance in the system porosity, which controls the mechanical properties of cement pastes. Copyright © 2016 Elsevier Inc. All rights reserved.

  17. 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.

  18. 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 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. PMID:27009966

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

    Directory of Open Access Journals (Sweden)

    Lu Zeng

    2014-01-01

    Full Text Available 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-first-order and pseudo-second-order kinetic models and intraparticle diffusion model. The pseudo-second-order model provided the best correlation and the intraparticle diffusion controlled the adsorption process of AFB1 onto CCSH. Adsorption isotherm parameters were obtained from Langmuir and Freundlich and the adsorption data fitted to Freundlich much better. Based on the results of N2 adsorption/desorption, adsorption kinetics, and adsorption isotherms, the adsorption mechanism of AFB1 onto CCSH was developed. All results indicate that CCSH has a great potential to be a safe, easy-made, and cost-effective material for the control of AFB1 contamination.

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

    Energy Technology Data Exchange (ETDEWEB)

    Myers, Rupert J., E-mail: rjmyers@sheffield.ac.uk [Department of Materials Science and Engineering, University of Sheffield, S1 3JD Sheffield (United Kingdom); Laboratory for Concrete and Construction Chemistry, EMPA, Dübendorf 8600 (Switzerland); L' Hôpital, Emilie, E-mail: Emilie.Lhopital@empa.ch [Laboratory for Concrete and Construction Chemistry, EMPA, Dübendorf 8600 (Switzerland); Provis, John L., E-mail: j.provis@sheffield.ac.uk [Department of Materials Science and Engineering, University of Sheffield, S1 3JD Sheffield (United Kingdom); Lothenbach, Barbara, E-mail: Barbara.Lothenbach@empa.ch [Laboratory for Concrete and Construction Chemistry, EMPA, Dübendorf 8600 (Switzerland)

    2015-02-15

    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.

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

    Energy Technology Data Exchange (ETDEWEB)

    Grangeon, Sylvain, E-mail: S.Grangeon@brgm.fr [BRGM, 3, Avenue Claude Guillemin, 45060 Orléans Cedex 2 (France); Claret, Francis; Lerouge, Catherine [BRGM, 3, Avenue Claude Guillemin, 45060 Orléans Cedex 2 (France); Warmont, Fabienne [CRMD, UMR 6619 – CNRS, 1b rue de la férollerie, 45071 Orléans Cedex 2 (France); Sato, Tsutomu; Anraku, Sohtaro [Laboratory of Environmental Geology, Research Group of Geoenvironmental/Engineering Division of Solid Waste, Resources and Geoenvironmental/Engineering Graduate School of Engineering, Hokkaido University, Kita 13 Nishi 8, Sapporo 060-8628 (Japan); Numako, Chiya [Faculty of Integrated Arts and Sciences, The University of Tokushima, 1-1, Minami-Josanjima, Tokushima, 770-8502 (Japan); Linard, Yannick [ANDRA, Centre de Meuse/Haute Marne, 55290 Bure (France); Lanson, Bruno [ISTerre, Grenoble University, CNRS, F-38041 Grenoble (France)

    2013-10-15

    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.

  2. 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.

  3. X-ray spectra and theoretical elastic properties of crystalline calcium silicate hydrates: comparison with cement hydrated gels

    Directory of Open Access Journals (Sweden)

    Ayuela, A.

    2010-09-01

    Full Text Available For 22 crystalline Calcium Silicates Hydrates, we have calculated their structure and their elastic properties by atomistic force field methods as well as simulate their Xray diffraction patterns. From the computed Young moduli, it can be suggested that the key parameters to determine the elastic properties of crystalline Calcium Silicate Hydrates are densities and water content. We have compared these trends with those of cementitious C-S-H gel and synthetic C-S-H type I as a function of their C/S ratios and nominal water content. Our comparison show that the experimentally suggested values of density and Young moduli for C-S-H gel lie in the range of the calculated CSH crystals. However, we conclude that a detailed correspondence might require investigating structurally within CSH gels the role of water and especially of Ca and Si sites through their C/S ratio.

    En este trabajo se han calculado para 22 Silicatos Cálcicos Hidratados cristalinos, su estructura y sus propiedades elásticas mediante métodos atomísticos “force field”, así como simulado sus espectros de difracción de rayos X. De los módulos de Young calculados se puede deducir, que los parámetros clave que determinan las propiedades elásticas de los Silicatos Cálcicos Hidratados cristalinos son la densidad y el contenido en agua. Nuestros resultados muestran que los valores experimentales de la densidad y de los módulos de Young para el gel C-S-H están dentro del rango de los cristales de CSH calculados. Sin embargo, podemos concluir que para establecer una correlación más directa sería necesario investigar el papel que juegan el agua y sobre todo el Ca y Si, mediante la relación C/S, en la estructura del gel CSH.

  4. Nanostructured calcium silicate hydrate seeds accelerate concrete hardening: a combined assessment of benefits and risks.

    Science.gov (United States)

    Bräu, Michael; Ma-Hock, Lan; Hesse, Christoph; Nicoleau, Luc; Strauss, Volker; Treumann, Silke; Wiench, Karin; Landsiedel, Robert; Wohlleben, Wendel

    2012-07-01

    Nanotechnology creates new possibilities to control and improve material properties for civil infrastructure. Special focus in this area is put on Portland cement and gypsum. Together their annual production is by far larger than for any other material worldwide. Nanomodification of these materials can be done during the few hours between dissolution and hardening, especially by nucleation of the re-crystallization with suitable colloids. Here we report first results in homogeneous seeding of the precipitation of calcium silicate hydrates within a real Portland cement composition. The occupational safety during the production phase and during mixing of concrete paste is addressed in detail by in vivo testing. We perform 5-day inhalation with 21-day recovery in rats and analyze organ-specific toxicity and 71 endpoints from bronchoalveolar lavage (BALF) and blood. In BALF parameters, no test-related changes were observed, indicating the generally low toxicity of the test material. Some mild lesions were observed in larynx level. In the lungs, all animals of the 50 mg/m³ concentration group revealed a minimal to mild increase in alveolar macrophages, which recovered back to control level.

  5. Effects of glass fiber modified with calcium silicate hydrate (C-S-H(I)) reinforced cement

    Science.gov (United States)

    Xin, M.; Zhang, L.; Ge, S.; Cheng, X.

    2017-03-01

    In this paper, calcium silicate hydrate (C-S-H(I)) and glass fiber modified with C-S-H(I) (SiF) at ambient temperature were synthesized. SiF and untreated fiber (OF) were incorporated into cement paste. Phase composition of C-S-H(I), SiF and OF was characterized by XRD. The surface morphologies were characterized by SEM. Flexural performance of fiber reinforced cement (FRC) at different curing ages was investigated. Results indicated that both SiF and OF could reinforce cement paste. SiF had a more positive effect on improving the flexural performance of FRC than OF. The strength of SiF reinforced cement was 11.48MPa after 28 days curing when fiber volume was 1.0%, 12.55% higher than that of OF reinforced cement. The flexural strength increased with the addition of fiber volume. However, the large dosage of fiber might cause a decrease in flexural strength of FRC.

  6. 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.

  7. Formation of hydrate films on the surface of calcium silicate and aluminate in the presence of polyelectrolytes

    Science.gov (United States)

    Kurochkina, G. N.

    2017-08-01

    To elucidate the mechanism of moistening and overmoistening of soils and mineral soil components capable of chemical hydration, the sorption of water vapor has been studied in combination with synchronous conductometric measurements. Effect of organic polyelectrolyte molecules on the hydration kinetics and the formation of hydrate films on their surface has been revealed for dehydrated calcium silicate and aluminate simulating minor soil components. The plotting of sorption-desorption curves has shown that hydrate-polymer films formed by aliphatic or aromatic polyelectrolytes with different functional groups (-COOH,-OH,-NH2,-CONH, etc.) significantly vary in dispersion and structure. The changes in dispersion during hydration are frequently not correlated with the amount of resulting hydrates, the content of which is controlled by the crystallochemical features of sorbents, the structure and activity of the polymer functional groups, and the conditions of sorption kinetic studies. It has been shown that the formation of low-permeable surface organomineral layers is typical for aliphatic polyelectrolytes, while more permeable layers determining the water-physical and structure-forming properties of soils are typical for aromatic polyelectrolytes.

  8. Characterization of the Bonds Developed between Calcium Silicate Hydrate and Polycarboxylate-Based Superplasticizers with Silyl Functionalities

    KAUST Repository

    Orozco, Carlos A.

    2017-03-24

    Major developments in concrete technology have been achieved with the use of polycarboxylate-based superplasticizers (PCEs) to improve the concrete rheology without increasing the mix water content. Currently, it is possible to control the fluidity of the fresh concrete and obtain stronger and more durable structures. Therefore, there is a strong incentive to understand the interactions between PCEs and cement hydrates at the atomic scale to design new customized functional PCEs according to the ever-increasing requirements of the concrete industry. Here, the bonding types generated between a PCE with silyl functionalities (PCE-Sil) and a synthetic calcium silicate hydrate (C-S-H) are analyzed using XRD, 29Si NMR spectroscopy, and synchrotron-based techniques, such as NEXAFS and EXAFS. The results indicated that the carboxylic groups present in PCE-Sil interact by a ligand-type bond with calcium, which modified not only the symmetry and coordination number of the calcium located at the surface of C-S-H but also the neighboring silicon atoms of the C-S-H. In addition, the silyl functionalities of the PCE-Sil generated covalent bonds through siloxane bridges between the silanol groups of PCE-Sil and the nonbonding oxygen located at the dimeric sites in C-S-H, forming new bridging silicon sites and subsequently increasing the silicate polymerization.

  9. Characterization of the Bonds Developed between Calcium Silicate Hydrate and Polycarboxylate-Based Superplasticizers with Silyl Functionalities.

    Science.gov (United States)

    Orozco, Carlos A; Chun, Byong W; Geng, Guoqing; Emwas, Abdul H; Monteiro, Paulo J M

    2017-04-11

    Major developments in concrete technology have been achieved with the use of polycarboxylate-based superplasticizers (PCEs) to improve the concrete rheology without increasing the mix water content. Currently, it is possible to control the fluidity of the fresh concrete and obtain stronger and more durable structures. Therefore, there is a strong incentive to understand the interactions between PCEs and cement hydrates at the atomic scale to design new customized functional PCEs according to the ever-increasing requirements of the concrete industry. Here, the bonding types generated between a PCE with silyl functionalities (PCE-Sil) and a synthetic calcium silicate hydrate (C-S-H) are analyzed using XRD, (29)Si NMR spectroscopy, and synchrotron-based techniques, such as NEXAFS and EXAFS. The results indicated that the carboxylic groups present in PCE-Sil interact by a ligand-type bond with calcium, which modified not only the symmetry and coordination number of the calcium located at the surface of C-S-H but also the neighboring silicon atoms of the C-S-H. In addition, the silyl functionalities of the PCE-Sil generated covalent bonds through siloxane bridges between the silanol groups of PCE-Sil and the nonbonding oxygen located at the dimeric sites in C-S-H, forming new bridging silicon sites and subsequently increasing the silicate polymerization.

  10. Structural and nano-mechanical properties of Calcium Silicate Hydrate (C-S-H) formed from alite hydration in the presence of sodium and potassium hydroxide

    Energy Technology Data Exchange (ETDEWEB)

    Mendoza, Oscar, E-mail: oamendoz@unal.edu.co [Grupo del Cemento y Materiales de Construcción (CEMATCO). Universidad Nacional de Colombia, Facultad de Minas, Medellín (Colombia); Giraldo, Carolina [Cementos Argos S.A., Medellín (Colombia); Camargo, Sergio S. [Engenharia Metalúrgica e de Materiais, Universidade Federal do Rio de Janeiro/COPPE, Rio de Janeiro (Brazil); Tobón, Jorge I. [Grupo del Cemento y Materiales de Construcción (CEMATCO). Universidad Nacional de Colombia, Facultad de Minas, Medellín (Colombia)

    2015-08-15

    This research evaluates the effect of sodium and potassium hydroxide on the structure and nano-mechanical properties of Calcium Silicate Hydrate (C-S-H) formed from the hydration of pure alite. Monoclinic (MIII) alite was synthesized and hydrated, using water-to-alite ratios of 0.5 and 0.6 and additions of 10% NaOH and KOH by weight of alite. Based on results of X-ray diffraction, isothermal calorimetry, thermogravimetric analysis, Nuclear Magnetic Resonance and nanoindentation, two different effects of the alkaline hydroxides on the hydration reaction of alite, both at early and later ages, can be identified: (i) a differentiated hydration process, attributed to an enhancement in calcium hydroxide (CH) precipitation and a stimulation of the C-S-H nuclei; and (ii) an increase in the elastic modulus of the C-S-H aggregations, attributed to an electrostatic attraction between positive charges from the alkaline cations and negative charges from the C-S-H structure.

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

    Energy Technology Data Exchange (ETDEWEB)

    Gallucci, E., E-mail: gallucci.emmanuel@ch.sika.com; Zhang, X.; Scrivener, K.L.

    2013-11-15

    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.

  12. 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)

  13. 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.

  14. Transformation of meta-stable calcium silicate hydrates to tobermorite: reaction kinetics and molecular structure from XRD and NMR spectroscopy

    Directory of Open Access Journals (Sweden)

    Carroll Susan A

    2009-01-01

    Full Text Available Abstract Understanding the integrity of well-bore systems that are lined with Portland-based cements is critical to the successful storage of sequestered CO2 in gas and oil reservoirs. As a first step, we investigate reaction rates and mechanistic pathways for cement mineral growth in the absence of CO2 by coupling water chemistry with XRD and NMR spectroscopic data. We find that semi-crystalline calcium (alumino-silicate hydrate (Al-CSH forms as a precursor solid to the cement mineral tobermorite. Rate constants for tobermorite growth were found to be k = 0.6 (± 0.1 × 10-5 s-1 for a solution:solid of 10:1 and 1.6 (± 0.8 × 10-4 s-1 for a solution:solid of 5:1 (batch mode; T = 150°C. This data indicates that reaction rates for tobermorite growth are faster when the solution volume is reduced by half, suggesting that rates are dependent on solution saturation and that the Gibbs free energy is the reaction driver. However, calculated solution saturation indexes for Al-CSH and tobermorite differ by less than one log unit, which is within the measured uncertainty. Based on this data, we consider both heterogeneous nucleation as the thermodynamic driver and internal restructuring as possible mechanistic pathways for growth. We also use NMR spectroscopy to characterize the site symmetry and bonding environment of Al and Si in a reacted tobermorite sample. We find two [4]Al coordination structures at δiso = 59.9 ppm and 66.3 ppm with quadrupolar product parameters (PQ of 0.21 MHz and 0.10 MHz (± 0.08 from 27Al 3Q-MAS NMR and speculate on the Al occupancy of framework sites by probing the protonation environment of Al metal centers using 27Al{1H}CP-MAS NMR.

  15. Multi-technology Investigation of the Atomic Structure of Calcium Silicate Hydrates

    Energy Technology Data Exchange (ETDEWEB)

    Geng, Guoqing; Kilcoyne, David A.; Benmore, Chris J.; Monteiro, Paul J.M.

    2015-01-01

    In this study, synthetic C-S-H samples were investigated to reveal the feature at atomic scale. Rietveld refinement was applied to high resolution X-ray scattering data, yielding the lattice constants of the pseudocrystal structure, as well as the crystallinity along three axes. Near Edge X-ray Absorption Fine Structure (NEXAFS) spectra was collected at calcium L3,2-edge. Evolution of calcium coordination symmetry were studied by investigating spectra characteristics. Pair Distribution Function (PDF) study yields the statistics of atom pair distribution. Coordination number of Ca and Si were obtained by integrating Radial distribution function. Atomic model based on dimeric structure were discussed and compared with experimental data. Synthetic C-S-H samples with increasing Ca/Si ratio exhibit pseudo-crystal structure, resembling Dreierketten configuration similar to natural tobermorite structure. Along c-axis, the repeated structure could not survives two layers in case of low Ca/Si ratio (0.70, 1.05). But in high Ca/Si ratio (1.42) case, the crystallinity along c-axis is much bigger. The coordination number of Ca decreases with increasing Ca/Si ratio. Octahedrally coordinated Ca are observed in sample with Ca/Si ratio of 1.42. Various dimeric models are compared with experimental data. In case of Ca/Si ratio of 1.42, SiO4 tetrahedron chain needs to be shortened in linkage, most probably by substituting bridging SiO4 tetrahedron with CaO6 octahedron. These octahedrons in interlayer space act like pins to join two adjacent layer structures together. The crystallinity is thus increased along c-axis, and average coordination number is therefore reduced. In case of Ca/Si 1.05, crystallinity is low along c-axis since, indicating that not too many Ca ions exist in interlayer space to hold two layers together. Instead, negative charge of end oxygen could be balanced by proton. Ca/Si 0.70 has long tetrahedron chain linkage within layer while the linkage between adjacent

  16. Quantitative X-ray pair distribution function analysis of nanocrystalline calcium silicate hydrates: a contribution to the understanding of cement chemistry.

    Science.gov (United States)

    Grangeon, Sylvain; Fernandez-Martinez, Alejandro; Baronnet, Alain; Marty, Nicolas; Poulain, Agnieszka; Elkaïm, Erik; Roosz, Cédric; Gaboreau, Stéphane; Henocq, Pierre; Claret, Francis

    2017-02-01

    The structural evolution of nanocrystalline calcium silicate hydrate (C-S-H) as a function of its calcium to silicon (Ca/Si) ratio has been probed using qualitative and quantitative X-ray atomic pair distribution function analysis of synchrotron X-ray scattering data. Whatever the Ca/Si ratio, the C-S-H structure is similar to that of tobermorite. When the Ca/Si ratio increases from ∼0.6 to ∼1.2, Si wollastonite-like chains progressively depolymerize through preferential omission of Si bridging tetrahedra. When the Ca/Si ratio approaches ∼1.5, nanosheets of portlandite are detected in samples aged for 1 d, while microcrystalline portlandite is detected in samples aged for 1 year. High-resolution transmission electron microscopy imaging shows that the tobermorite-like structure is maintained to Ca/Si > 3.

  17. 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.

  18. 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.

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

    NARCIS (Netherlands)

    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

  20. 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)

  1. Compositional Evolution of Calcium Silicate Hydrate (C-S-H) Structures by Total X-Ray Scattering

    KAUST Repository

    Soyer-Uzun, Sezen

    2011-12-09

    High-energy X-ray diffraction was employed to study the structural characteristics of a set of C-S-H samples with 0.6 ≤ C/S a;circ 1.75. It has been observed that Si is tetrahedrally coordinated to O for all samples irrespective of chemical composition and the Ca-O coordination number gradually decreases from ∼7 to ∼6 with increasing C/S ratio. This suggests that the C-S-H structure evolves from a tobermorite-like structure into a jennite-like structure as a function of increasing C/S ratio as the interlayer space decreases from ∼1.3 to ∼1 nm. Evolution of these short- and medium-range order structural characteristics in the C-S-H system is associated with the alteration of the Ca-O layers and silicate depolymerization with increasing C/S. © 2011 The American Ceramic Society.

  2. 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

  3. Investigation of the hydration and bioactivity of radiopacified tricalcium silicate cement, Biodentine and MTA Angelus.

    Science.gov (United States)

    Camilleri, Josette; Sorrentino, François; Damidot, Denis

    2013-05-01

    Novel root-end filling materials are composed of tricalcium silicate (TCS) and radiopacifier as opposed to the traditional mineral trioxide aggregate (MTA) which is made up of clinker derived from Portland cement and bismuth oxide. The aim of this research was to characterize and investigate the hydration of a tricalcium silicate-based proprietary brand cement (Biodentine™) and a laboratory manufactured cement made with a mixture of tricalcium silicate and zirconium oxide (TCS-20-Z) and compare their properties to MTA Angelus™. The materials investigated included a cement containing 80% of TCS and 20% zirconium oxide (TCS-20-Z), Biodentine™ and MTA Angelus™. The specific surface area and the particle size distribution of the un-hydrated cements and zirconium oxide were investigated using a gas adsorption method and scanning electron microscopy. Un-hydrated cements and set materials were tested for mineralogy and microstructure, assessment of bioactivity and hydration. Scanning electron microscopy, X-ray energy dispersive analysis, X-ray fluorescence spectroscopy, X-ray diffraction, Rietveld refined X-ray diffraction and calorimetry were employed. The radiopacity of the materials was investigated using ISO 6876 methods. The un-hydrated cements were composed of tricalcium silicate and a radiopacifier phase; zirconium oxide for both Biodentine™ and TCS-20-Z whereas bismuth oxide for MTA Angelus™. In addition Biodentine™ contained calcium carbonate particles and MTA Angelus™ exhibited the presence of dicalcium silicate, tricalcium aluminate, calcium, aluminum and silicon oxides. TCS and MTA Angelus™ exhibited similar specific surface area while Biodentine™ had a greater specific surface area. The cements hydrated and produced some hydrates located either as reaction rim around the tricalcium silicate grain or in between the grains at the expense of volume containing the water initially present in the mixture. The rate of reaction of tricalcium

  4. 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

  5. In Situ Soft X-ray Spectromicroscopy of Early Tricalcium Silicate Hydration

    Science.gov (United States)

    Bae, Sungchul; Kanematsu, Manabu; Hernández-Cruz, Daniel; Moon, Juhyuk; Kilcoyne, David; Monteiro, Paulo J. M.

    2016-01-01

    The understanding and control of early hydration of tricalcium silicate (C3S) is of great importance to cement science and concrete technology. However, traditional characterization methods are incapable of providing morphological and spectroscopic information about in situ hydration at the nanoscale. Using soft X-ray spectromicroscopy, we report the changes in morphology and molecular structure of C3S at an early stage of hydration. In situ C3S hydration in a wet cell, beginning with induction (~1 h) and acceleration (~4 h) periods of up to ~8 h, was studied and compared with ex situ measurements in the deceleration period after 15 h of curing. Analysis of the near-edge X-ray absorption fine structure showed that the Ca binding energy and energy splitting of C3S changed rapidly in the early age of hydration and exhibited values similar to calcium silicate hydrate (C–S–H). The formation of C–S–H nanoseeds in the C3S solution and the development of a fibrillar C–S–H morphology on the C3S surface were visualized. Following this, silicate polymerization accompanied by C–S–H precipitation produced chemical shifts in the peaks of the main Si K edge and in multiple scattering. However, the silicate polymerization process did not significantly affect the Ca binding energy of C–S–H. PMID:28774096

  6. In Situ Soft X-ray Spectromicroscopy of Early Tricalcium Silicate Hydration

    Directory of Open Access Journals (Sweden)

    Sungchul Bae

    2016-12-01

    Full Text Available The understanding and control of early hydration of tricalcium silicate (C3S is of great importance to cement science and concrete technology. However, traditional characterization methods are incapable of providing morphological and spectroscopic information about in situ hydration at the nanoscale. Using soft X-ray spectromicroscopy, we report the changes in morphology and molecular structure of C3S at an early stage of hydration. In situ C3S hydration in a wet cell, beginning with induction (~1 h and acceleration (~4 h periods of up to ~8 h, was studied and compared with ex situ measurements in the deceleration period after 15 h of curing. Analysis of the near-edge X-ray absorption fine structure showed that the Ca binding energy and energy splitting of C3S changed rapidly in the early age of hydration and exhibited values similar to calcium silicate hydrate (C–S–H. The formation of C–S–H nanoseeds in the C3S solution and the development of a fibrillar C–S–H morphology on the C3S surface were visualized. Following this, silicate polymerization accompanied by C–S–H precipitation produced chemical shifts in the peaks of the main Si K edge and in multiple scattering. However, the silicate polymerization process did not significantly affect the Ca binding energy of C–S–H.

  7. 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 Cosmetic Ingredient Review (CIR. The Cosmetic Ingredient Review (CIR) Expert Panel concluded that the extensive pulmonary damage in humans was the result of direct occupational inhalation of the dusts and noted that lesions seen in animals were affected by particle size, fiber length, and concentration. The Panel considers that most of the formulations are not respirable and of the preparations that are respirable, the concentration of the ingredient is very low. Even so, the Panel considered that any spray containing these solids should be formulated to minimize their inhalation. With this admonition to the cosmetics industry, the CIR Expert Panel concluded that these ingredients are safe as currently used in cosmetic formulations. The Panel did note that the cosmetic ingredient, Talc, is a hydrated magnesium silicate. Because it has a unique crystalline structure that differs from ingredients addressed in this safety assessment, Talc is not included in this report.

  8. Characterization of set Intermediate Restorative Material, Biodentine, Bioaggregate and a prototype calcium silicate cement for use as root-end filling materials.

    Science.gov (United States)

    Grech, L; Mallia, B; Camilleri, J

    2013-07-01

    To investigate the composition of materials and leachate of a hydrated prototype cement composed of tricalcium silicate and radiopacifier and compare this to other tricalcium silicate-based cements (Biodentine and Bioaggregate) to assess whether the additives in the proprietary brand cements affect the hydration of the materials, using Intermediate Restorative Material (IRM), a standard root-end filling material as a control. The materials investigated included a prototype-radiopacified tricalcium silicate cement, Biodentine, Bioaggregate and Intermediate Restorative Material (IRM). The pH and calcium ion concentration of the leachate were investigated. The hydrated cements were characterized using scanning electron microscopy (SEM) and X-ray energy dispersive analysis (EDX), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). All the cements tested were alkaline. The tricalcium silicate-based cements leached calcium in solution. Scanning electron microscopy of the prototype-radiopacified tricalcium silicate cement, Biodentine and Bioaggregate displayed hydrating cement grains, surrounded by a matrix composed of calcium silicate hydrate and calcium hydroxide. The presence of calcium hydroxide was evident from the XRD plots. FT-IR indicated the occurrence of a poorly crystalline calcium silicate hydrate. Biodentine displayed the presence of calcium carbonate. Bioaggregate incorporated a phosphate-containing phase. IRM consisted of zinc oxide interspersed in an organic matrix. The hydration of prototype-radiopacified tricalcium silicate cement, Biodentine and Bioaggregate resulted in the formation of calcium silicate hydrate and calcium hydroxide, which was leached in solution. The hydrated materials were composed of a cementitous phase that was rich in calcium and silicon and a radiopacifying material. Biodentine included calcium carbonate, and Bioaggregate included silica and calcium phosphate in the powders. IRM was composed of zinc oxide

  9. Hydration modelling of calcium sulphates

    NARCIS (Netherlands)

    de Korte, A.C.J.; Eligehausen, R.; Gehlen, C.

    2008-01-01

    The CEMHYD3D model has been extended at the University of Twente in last ten years1,2. At present the cement hydration model is extended for the use of gypsum. Although gypsum was present in the model already, the model was not suitable for high contents of gypsum and did not include the transitions

  10. 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

    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...... 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 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...

  11. Hydration of Biodentine, Theracal LC, and a prototype tricalcium silicate-based dentin replacement material after pulp capping in entire tooth cultures.

    Science.gov (United States)

    Camilleri, Josette; Laurent, Patrick; About, Imad

    2014-11-01

    The calcium-releasing ability of pulp-capping materials induces pulp tissue regeneration. Tricalcium silicate-based materials produce calcium hydroxide as a by-product of hydration. Assessment of hydration and calcium ion leaching is usually performed on samples that have been aged in physiological solution for a predetermined period of time. The hydration and activity of the materials in vivo may not be similar to those displayed in vitro because of insufficient fluid available in contact with dentin. The aim of this research was the assessment of hydration of Biodentine, Theracal LC, and a prototype radiopacified tricalcium silicate-based material after pulp capping and to compare it with direct hydration in an aqueous solution. The extent of hydration of Biodentine, Theracal LC, and a prototype radiopacified tricalcium silicate-based material with a similar composition to Biodentine but not incorporating the additives was assessed by scanning electron microscopy and energy dispersive spectroscopy of polished specimens after being allowed to hydrate in Hank's balanced salt solution for 14 days. The extent of hydration was compared with material hydration when used as direct pulp capping materials by using a tooth culture model. Material activity was also assessed by x-ray diffraction analysis to investigate the deposition of calcium hydroxide by the materials, and calcium ion leaching in Hank's balanced salt solution was assessed by ion chromatography. Biodentine and the prototype tricalcium silicate cement hydrated and reaction by-products were deposited in the cement matrix both after pulp capping and when incubated in an aqueous solution. Calcium hydroxide was formed, and calcium ions were leached in solution. Theracal LC hydration was incomplete because of the limited moisture diffusion within the material. Thus, no calcium hydroxide was produced, and a lower calcium ion leaching was recorded. Theracal LC had a heterogeneous structure with large unhydrated

  12. Effect of phase composition of calcium silicate phosphate component on properties of brushite based composite cements

    Energy Technology Data Exchange (ETDEWEB)

    Sopcak, T., E-mail: tsopcak@imr.saske.sk [Institute of Materials Research of SAS, Watsonova 47, 04001 Kosice (Slovakia); Medvecky, L.; Giretova, M.; Stulajterova, R.; Durisin, J. [Institute of Materials Research of SAS, Watsonova 47, 04001 Kosice (Slovakia); Girman, V. [Institute of Physics, Faculty of Science, P. J. Šafárik University, Park Angelinum 9, 04001 Kosice (Slovakia); Faberova, M. [Institute of Materials Research of SAS, Watsonova 47, 04001 Kosice (Slovakia)

    2016-07-15

    The composite cement mixtures were prepared by mixing brushite (B) with, the amorphous hydrated calcium silicate phosphate (CSPH) or annealed calcium silicate phosphate (CSP composed of Si-saturated hydroxyapatite, wollastonite and silica) phases and water as liquid component. The contents of the silicate-phosphate phase in composites were 10.30 and 50 wt%. The significant effect of both the Ca/P ratio and different solubility of calcium silicate phosphate component in starting cement systems on setting time and phase composition of the final composite cements was demonstrated. The compressive strength of the set cements increased with the filler addition and the highest value (~ 48 MPa) exhibited the 50CSP/B cement composite. The final setting times of the composite cements decreased with the CSPH addition from about 25 to 17 min in 50CSHP/B and setting time of CSP/B composites was around 30 min. The higher content of silica in cements caused the precipitation of fine hydroxyapatite particles in the form of nanoneedles or thin plates perpendicularly oriented to sample surface. The analysis of in vitro cement cytotoxicity demonstrated the strong reduction in cytotoxicity of 10CSPH/B composite with time of cultivation (a low cytotoxicity after 9 days of culture) contrary to cements with higher calcium silicate-phosphate content. These results were attributed to the different surface topography of composite substrates and possible stimulation of cell proliferation by the slow continuously release of ions from 10CSPH/B cement. - Highlights: • Ca/P ratio and solubility of calcium silicate-phosphate components affect the self-setting properties of cements. • Strong relationship between the composite in vitro cytotoxicity and surface microtopography was demonstrated. • Plate-like morphology of coarser particles allowed cells to better adhere and proliferate as compared with nanoneedles.

  13. 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.

  14. 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.

  15. Potential of calcium silicate to mitigate water deficiency in maize

    Directory of Open Access Journals (Sweden)

    Douglas José Marques

    2016-01-01

    Full Text Available ABSTRACT The aim of this study was to evaluate the potential of calcium silicate to mitigate the effects of water deficiency in maize plants yield. A completely randomized factorial design, consisting of five combinations of calcium silicate (0, 25, 50, 75, and 100% and five different soil moisture levels (30, 70, 100, 130, and 160%, was adopted. The following parameters were evaluated: soil matric potential, xylem water potential, silicon concentration, leaf dry weight, and dry mass production. Matric potential monitoring confirmed that the irrigation depths employed resulted in different environments for maize plant development during the experiment. Confirming the hypothesis of the study, at the lower irrigation depths, the maize production has accompanied the increase in calcium silicate used as corrective up to the proportion of 50%. These results indicate that silicon mitigated the impact of water deficiency in maize plants and increased the xylem water potential.

  16. 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

  17. Evaluation of Calcium Silicate Cement Bond Strength after Using ...

    African Journals Online (AJOL)

    2018-01-24

    Jan 24, 2018 ... Objectives: To determine the effect of different gutta‑percha solvents. (chloroform, Endosolv E, orange oil, and eucalyptol) on the push‑out bond strength of calcium silicate cements (CSCs; white mineral trioxide aggregate. [WMTA]; capsule‑form mineral trioxide aggregate [CMTA], and Biodentine). Materials ...

  18. Water transport in the nano-pore of the calcium silicate phase: reactivity, structure and dynamics.

    Science.gov (United States)

    Hou, Dongshuai; Li, Zongjin; Zhao, Tiejun; Zhang, Peng

    2015-01-14

    Reactive force field molecular dynamics was utilized to simulate the reactivity, structure and dynamics of water molecules confined in calcium-silicate-hydrate (C-S-H) nano-pores of 4.5 nm width. Due to the highly reactive C-S-H surface, hydrolytic reactions occur in the solid-liquid interfacial zone, and partially surface adsorbed water molecules transforming into the Si-OH and Ca-OH groups are strongly embedded in the C-S-H structure. Due to the electronic charge difference, the silicate and calcium hydroxyl groups have binomial distributions of the dipolar moment and water orientation. While Ca-OH contributes to the Ow-downward orientation, the ONB atoms in the silicate chains prefer to accept H-bonds from the surface water molecules. Furthermore, the defective silicate chains and solvated Caw atoms near the surface contribute to the glassy nature of the surface water molecules, with large packing density, pronounced orientation preference, and distorted organization. The stable H-bonds connected with the Ca-OH and Si-OH groups also restrict the mobility of the surface water molecules. The significant reduction of the diffusion coefficient matches well with the experimental results obtained by NMR, QENS and PCFR techniques. Upon increasing the distance from the channel, the structural and dynamic behavior of the water molecules varies and gradually translates into bulk water properties at distances of 10-15 Å from the liquid-solid interface.

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

    Directory of Open Access Journals (Sweden)

    Yoshiyuki Kojima

    2012-01-01

    Full Text Available 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 Tb3+-activated amorphous calcium silicate emitted green by ultraviolet irradiation. The optimum initial Tb/Ca atomic ratio of this phosphor was about 0.5. A mechanism for the action of the phosphor is proposed, in which Tb3+ ions existing in the layer of the CSH lead to loss of water molecules and OH groups.

  20. Chemical characteristics of mineral trioxide aggregate and its hydration reaction

    OpenAIRE

    Seok-Woo Chang

    2012-01-01

    Mineral trioxide aggregate (MTA) was developed in early 1990s and has been successfully used for root perforation repair, root end filling, and one-visit apexification. MTA is composed mainly of tricalcium silicate and dicalcium silicate. When MTA is hydrated, calcium silicate hydrate (CSH) and calcium hydroxide is formed. Formed calcium hydroxide interacts with the phosphate ion in body fluid and form amorphous calcium phosphate (ACP) which finally transforms into calcium deficient hydroxyap...

  1. 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 cementsbismuth on cell proliferation was reduced by the progressive increase of the biocoating thickness on aged cement. In conclusion, the experimental cements have adequate biological properties to be used as root-end/root repair filling materials or pulp capping materials. The alfa-TCP doped cement represents a new potential bioactive material for expanded applications in

  2. Gravimetric Determination of Calcium as Calcium Carbonate Hydrate.

    Science.gov (United States)

    Henrickson, Charles H.; Robinson, Paul R.

    1979-01-01

    The gravimetric determination of calcium as calcium carbonate is described. This experiment is suitable for undergraduate quantitative analysis laboratories. It is less expensive than determination of chloride as silver chloride. (BB)

  3. 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).

  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

    Abstract 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. 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.

  6. Measurement of the efficacy of calcium silicate for the protection and repair of dental enamel.

    Science.gov (United States)

    Parker, Alexander S; Patel, Anisha N; Al Botros, Rehab; Snowden, Michael E; McKelvey, Kim; Unwin, Patrick R; Ashcroft, Alexander T; Carvell, Mel; Joiner, Andrew; Peruffo, Massimo

    2014-06-01

    To investigate the formation of hydroxyapatite (HAP) from calcium silicate and the deposition of calcium silicate onto sound and acid eroded enamel surfaces in order to investigate its repair and protective properties. Calcium silicate was mixed with phosphate buffer for seven days and the resulting solids analysed for crystalline phases by Raman spectroscopy. Deposition studies were conducted on bovine enamel surfaces. Acid etched regions were produced on the enamel surfaces using scanning electrochemical cell microscopy (SECCM) with acid filled pipettes and varying contact times. Following treatment with calcium silicate, the deposition was visualised with FE-SEM and etch pit volumes were measured by AFM. A second set of bovine enamel specimens were pre-treated with calcium silicate and fluoride, before acid exposure with the SECCM. The volumes of the resultant acid etched pits were measured using AFM and the intrinsic rate constant for calcium loss was calculated. Raman spectroscopy confirmed that HAP was formed from calcium silicate. Deposition studies demonstrated greater delivery of calcium silicate to acid eroded than sound enamel and that the volume of acid etched enamel pits was significantly reduced following one treatment (penamel was 0.092 ± 0.008 cm/s. This was significantly reduced, 0.056 ± 0.005 cm/s, for the calcium silicate treatments (penamel surfaces. Calcium silicate can provide significant protection of sound enamel from acid challenges. Calcium silicate is a material that has potential for a new approach to the repair of demineralised enamel and the protection of enamel from acid attacks, leading to significant dental hard tissue benefits. © 2014 Elsevier Ltd. All rights reserved.

  7. Influence of iron on crystallization behavior and thermal stability of the insulating materials - porous calcium silicates

    DEFF Research Database (Denmark)

    Haastrup, Sonja; Yu, Donghong; Yue, Yuanzheng

    2017-01-01

    The properties of porous calcium silicate for high temperature insulation are strongly influenced by impurities. In this work we determine the influence of Fe3+ on the crystallization behavior and thermal stability of hydrothermally derived calcium silicate. We synthesize porous calcium silicate...... by XRD analysis. The thermal stability and compressive strength of the calcium silicates are seriously influenced by the changes of their crystal structure. Linear shrinkage of the reference sample is 1.3% at 1050°C, whereas the sample with Fe/Si =1.0% does by 30.4%. In conclusion, the presence of Fe3......+ modifies the crystal structure of porous calcium silicates, leading to a significant shrinkage in these materials....

  8. Calcium bromide hydration for heat storage systems

    OpenAIRE

    Ai Niwa; Noriyuki Kobayashi

    2015-01-01

    A chemical reaction is a common and simple way to produce heat for a heat storage system. The reaction produces heat energy without the use of electricity or fuel. The goal of this study was to develop a heat storage system for use in automobiles, which is able to provide heat rapidly via a hydration reaction. A heat storage system without an evaporator stores high-density heat and has a high heat output rate since the solid–liquid product that is formed is transferred as a heat medium to the...

  9. Calcium bromide hydration for heat storage systems

    Directory of Open Access Journals (Sweden)

    Ai Niwa

    2015-12-01

    Full Text Available A chemical reaction is a common and simple way to produce heat for a heat storage system. The reaction produces heat energy without the use of electricity or fuel. The goal of this study was to develop a heat storage system for use in automobiles, which is able to provide heat rapidly via a hydration reaction. A heat storage system without an evaporator stores high-density heat and has a high heat output rate since the solid–liquid product that is formed is transferred as a heat medium to the object that requires heat. The exothermic heat produced from the solid–liquid reaction was measured, and the relationship between the equivalence ratio and the reaction heat was evaluated. The heat output and heat recovered by the heat storage system, which comprised a reaction vessel and a heat exchanger, were measured. We selected solid CaBr2 because it was the best metal halide for a hydration reaction and had a high heat yield from the dissolution reaction. With this system, we were able to achieve a heat recovery rate of 582 kJ/L-H2O. We found no degradation in the chemical composition of CaBr2 after it being recycled 100 times.

  10. A multinuclear solid state NMR spectroscopic study of the structural evolution of disordered calcium silicate sol-gel biomaterials.

    Science.gov (United States)

    Lin, Zhongjie; Jones, Julian R; Hanna, John V; Smith, Mark E

    2015-01-28

    Disordered sol-gel prepared calcium silicate biomaterials show significant, composition dependent ability to bond with bone. Bone bonding is attributed to rapid hydroxycarbonate apatite (HCA) formation on the glass surface after immersion in body fluid (or implantation). Atomic scale details of the development of the structure of (CaO)x(SiO2)1-x (x = 0.2, 0.3 and 0.5) under heat treatment and subsequent dissolution in simulated body fluid (SBF) are revealed through a multinuclear solid state NMR approach using one-dimensional (17)O, (29)Si, (31)P and (1)H. Central to this study is the combination of conventional static and magic angle spinning (MAS) and two-dimensional (2D) triple quantum (3Q) (17)O NMR experiments that can readily distinguish and quantify the bridging (BOs) and non-bridging (NBOs) oxygens in the silicate network. Although soluble calcium is present in the sol, the (17)O NMR results reveal that the sol-gel produced network structure is initially dominated by BOs after gelation, aging and drying (e.g. at 120 °C), indicating a nanoscale mixture of the calcium salt and a predominantly silicate network. Only once the calcium salt is decomposed at elevated temperatures do the Ca(2+) ions become available to break BO. Apatite forming ability in SBF depends strongly on the surface OH and calcium content. The presence of calcium aids HCA formation via promotion of surface hydration and the ready availability of Ca(2+) ions. (17)O NMR shows the rapid loss of NBOs charge balanced by calcium as it is leached into the SBF. The formation of nanocrystalline, partially ordered HCA can be detected via(31)P NMR. This data indicates the importance of achieving the right balance of BO/NBO for optimal biochemical response and network properties.

  11. In vitro cytotoxicity of calcium silicate-containing endodontic sealers.

    Science.gov (United States)

    Zhou, Hui-min; Du, Tian-feng; Shen, Ya; Wang, Zhe-jun; Zheng, Yu-feng; Haapasalo, Markus

    2015-01-01

    The cytotoxicity of 2 novel calcium silicate-containing endodontic sealers to human gingival fibroblasts was studied. EndoSequence BC (Brasseler, Savannah, GA), MTA Fillapex (Angelus Indústria de Produtos Odontológicos S/A, Londrina, PR, Brazil) and a control sealer (AH Plus; Dentsply DeTrey GmbH, Konstanz, Germany) were evaluated. Human gingival fibroblasts were incubated for 3 days both with the extracts from fresh and set materials in culture medium and cultured on the surface of the set materials in Dulbecco-modified Eagle medium. Fibroblasts cultured in Dulbecco-modified Eagle medium were used as a control group. Cytotoxicity was evaluated by flow cytometry, and the adhesion of the fibroblasts to the surface of the set materials was assessed using scanning electron microscopy. The data of cell cytotoxicity were analyzed statistically using a 1-way analysis of variance test at a significance level of P extracts from BC Sealer showed higher viabilities at all extract concentrations than cells incubated with extracts from freshly mixed AH Plus and fresh and set MTA Fillapex, esspecially for the high extract concentrations (1:2 and 1:8 dilutions). Extracts from set MTA Fillapex of 2 weeks and older were more cytotoxic than extracts from freshly mixed and 1-week-old cement. With extract concentrations of 1:32 and lower, MTA Fillapex was no longer cytotoxic. After setting, AH Plus was no longer cytotoxic, and the fibroblast cells grew on set AH Plus equally as well as on BC Sealer. BC Sealer and MTA Fillapex, the 2 calcium silicate-containing endodontic sealers, exhibited different cytotoxicity to human gingival fibroblasts. Copyright © 2015 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  12. 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.

  13. Comparison of Ferrous Calcium Silicate Slag and Calcium Ferrite Slag Interactions with Magnesia-Chrome Refractories

    Science.gov (United States)

    Kaur, R. R.; Swinbourne, D. R.; Wadsley, M. W.; Nexhip, C.

    2011-06-01

    The cost of maintaining and eventually replacing refractories as a result of slag attack is a significant cost component in the copper industry. Converting matte to blister copper takes place in reactors lined with direct-bonded magnesia-chrome refractories, and several continuous converting operations use calcium ferrite slag. Unfortunately, the low viscosity of calcium ferrite slag makes it aggressive toward the refractories. Ferrous calcium silicate (FCS) slag has been proposed as a replacement; however, the effect of this slag on magnesia-chrome refractories has not been studied. In this work, the interactions between FCS slag and magnesia-chrome refractory at 1573 K (1300 °C) with an oxygen partial pressure of 10-6 atm were studied and compared with that experienced with calcium ferrite slag under the same conditions. Both slags penetrated the pores in the refractory and caused compositional change in the chromite spinel intergranular bonding phase through cation interdiffusion, which resulted in cracking and debonding of periclase grains. It was observed that the refractory was penetrated much more deeply by calcium ferrite slag than FCS slag because of the higher surface tension and lower viscosity of calcium ferrite slag. As a result, the refractory was attacked less by FCS slag than it was by calcium ferrite slag. It is concluded that the use of FCS slag in continuous copper converting is likely to extend refractory life.

  14. 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.

  15. Modeling Nanomechanical Behavior of Calcium-Silicate-Hydrate

    Science.gov (United States)

    2012-08-01

    Figure 13. The indentation force versus indentation depth for specimens with packing ratios of 0.56, 0.64 and 0.74. The snap shots show the progression...Based on experimental data from Atomic Force Microscope (AFM; Nonat 2004), small angle neutron scattering (SANS; Allen et al. 2007), Transmission...ratios of 0.56, 0.64 and 0.74. The snap shots show the progression of indented particle assembly. The color shows the stresses in the vertical

  16. Mesoporous Calcium Silicate Nanoparticles with Drug Delivery and Odontogenesis Properties.

    Science.gov (United States)

    Huang, Ching-Yuang; Huang, Tsui-Hsien; Kao, Chia-Tze; Wu, Yuan-Haw; Chen, Wan-Chen; Shie, Ming-You

    2017-01-01

    Calcium silicate (CS) -based materials play an important role in the development of endodontic materials that induce bone/cementum tissue regeneration and inhibit bacterial viability. The aim of this study was to prepare novel mesoporous CS (MesoCS) nanoparticles that have osteogenic, drug delivery, and antibacterial characteristics for endodontic materials and also have an excellent ability to develop apatite mineralization. The MesoCS nanoparticles were prepared using sol-gel methods. In addition, the mesoporous structure, specific surface area, pore volume, and morphology of the MesoCS nanoparticles were analyzed. The apatite mineralization ability, in vitro odontogenic differentiation, drug delivery, and antibacterial properties of the MesoCS nanoparticles were further investigated. The results indicate that the 200-nm-sized MesoCS nanoparticles synthesized using a facile template method exhibited a high specific surface area and pore volume with internal mesopores (average pore size = 3.05 nm). Furthermore, the MesoCS nanoparticles can be used as drug carriers to maintain sustained release of gentamicin and fibroblast growth factor-2 (FGF-2). The MesoCS-loaded FGF-2 might stimulate more odontogenic-related protein than CS because of the FGF-2 release. Based on this work, it can be inferred that MesoCS nanoparticles are potentially useful endodontic materials for biocompatible and osteogenic dental pulp tissue regenerative materials. Copyright © 2016 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  17. Nanoporous Calcium Silicate and PLGA Biocomposite for Bone Repair

    Directory of Open Access Journals (Sweden)

    Jiacan Su

    2010-01-01

    Full Text Available Nanoporous calcium silicate (n-CS with high surface area was synthesized using the mixed surfactants of EO20PO70EO20 (polyethylene oxide20(polypropylene oxide70(polyethylene oxide20, P123 and hexadecyltrimethyl ammonium bromide (CTAB as templates, and its composite with poly(lactic acid-co-glycolic acid (PLGA were fabricated. The results showed that the n-CS/PLGA composite (n-CPC with 20 wt% n-CS could induce a dense and continuous layer of apatite on its surface after soaking in simulated body fluid (SBF for 1 week, suggesting the excellent in vitro bioactivity. The n-CPC could promote cell attachment on its surfaces. In addition, the proliferation ratio of MG63 cells on n-CPC was significantly higher than PLGA; the results demonstrated that n-CPC had excellent cytocompatibility. We prepared n-CPC scaffolds that contained open and interconnected macropores ranging in size from 200 to 500 μm. The n-CPC scaffolds were implanted in femur bone defect of rabbits, and the in vivo biocompatibility and osteogenicity of the scaffolds were investigated. The results indicated that n-CPC scaffolds exhibited good biocompatibility, degradability, and osteogenesis in vivo. Collectively, these results suggested that the incorporation of n-CS in PLGA produced biocomposites with improved bioactivity and biocompatibility.

  18. Control of drying shrinkage in magnesium silicate hydrate (M-S-H) gel mortars

    OpenAIRE

    Zhang, T; Liang, X; Li, C; Lorin, M; Li, Y; Vandeperre, LJM; Cheeseman, CR

    2016-01-01

    ? 2016 Elsevier Ltd. All rights reserved.Magnesium silicate hydrate (M-S-H) gel can be formed by the reaction of MgO with amorphous silica in the presence of sodium hexametaphosphate (Na-HMP). Typical pastes contain 40% MgO and 60% SF and have a w/c ratio of 0.5, but these exhibit shrinkage cracking on drying. The shrinkage characteristics of M-S-H mortar samples containing different additions of sand have been studied using dilatometry. The drying shrinkage was found to decrease with increas...

  19. Fluorescent properties of a blue-to green-emitting Ce{sup 3+}, Tb{sup 3+} codoped amorphous calcium silicate phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Kojima, Yoshiyuki, E-mail: kojima.yoshiyuki@nihon-u.ac.jp [Department of Materials and Applied Chemistry, Faculty of Science and Engineering, Nihon University, 1-8, Kanda-Surugadai, Chiyoda-ku, Tokyo 101-8308 (Japan); Numazawa, Masaaki; Umegaki, Tetsuo [Department of Materials and Applied Chemistry, Faculty of Science and Engineering, Nihon University, 1-8, Kanda-Surugadai, Chiyoda-ku, Tokyo 101-8308 (Japan)

    2012-11-15

    Ce{sup 3+}, Tb{sup 3+} codoped amorphous calcium silicate phosphor was prepared by heating (830 Degree-Sign C for 30 min) Ce{sup 3+}, Tb{sup 3+} 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 {sup 5}D{sub 4}{yields}{sup 7}F{sub 5} transition of Tb{sup 3+}, and at 430-470 mm, attributed to Ce{sup 3+}. The intensity ratio of the two peaks could be freely controlled by varying the Tb/Ca atomic ratio of the Ce{sup 3+}, Tb{sup 3+} 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 Ce{sup 3+} to Tb{sup 3+}. - Graphical abstract: Ce{sup 3+}, Tb{sup 3+} codoped calcium silicate hydrate phosphor was synthesized by liquid-phase reaction. This was heated at 830 Degree-Sign C to obtain a Ce{sup 3+}, Tb{sup 3+} 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 Ce{sup 3+} to Tb{sup 3+} is occurring.

  20. 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.

  1. Total allowable concentrations of monomeric inorganic aluminum and hydrated aluminum silicates in drinking water.

    Science.gov (United States)

    Willhite, Calvin C; Ball, Gwendolyn L; McLellan, Clifton J

    2012-05-01

    Maximum contaminant levels are used to control potential health hazards posed by chemicals in drinking water, but no primary national or international limits for aluminum (Al) have been adopted. Given the differences in toxicological profiles, the present evaluation derives total allowable concentrations for certain water-soluble inorganic Al compounds (including chloride, hydroxide, oxide, phosphate and sulfate) and for the hydrated Al silicates (including attapulgite, bentonite/montmorillonite, illite, kaolinite) in drinking water. The chemistry, toxicology and clinical experience with Al materials are extensive and depend upon the particular physical and chemical form. In general, the water solubility of the monomeric Al materials depends on pH and their water solubility and gastrointestinal bioavailability are much greater than that of the hydrated Al silicates. Other than Al-containing antacids and buffered aspirin, food is the primary source of Al exposure for most healthy people. Systemic uptake of Al after ingestion of the monomeric salts is somewhat greater from drinking water (0.28%) than from food (0.1%). Once absorbed, Al accumulates in bone, brain, liver and kidney, with bone as the major site for Al deposition in humans. Oral Al hydroxide is used routinely to bind phosphate salts in the gut to control hyperphosphatemia in people with compromised renal function. Signs of chronic Al toxicity in the musculoskeletal system include a vitamin D-resistant osteomalacia (deranged membranous bone formation characterized by accumulation of the osteoid matrix and reduced mineralization, reduced numbers of osteoblasts and osteoclasts, decreased lamellar and osteoid bands with elevated Al concentrations) presenting as bone pain and proximal myopathy. Aluminum-induced bone disease can progress to stress fractures of the ribs, femur, vertebrae, humerus and metatarsals. Serum Al ≥100 µg/L has a 75-88% positive predictive value for Al bone disease. Chronic Al

  2. Examination of Cement Pastes Hydrated Phases, and Synthetic Products by X-Ray Diffraction

    Science.gov (United States)

    1972-04-01

    F. E. Jones, Hydration of Calcium Aluminates and Ferrites , Fourth International Symposium on the Chemistry of Cement, Washington, D. C., 1960, Vol 1...hydrated calcium aluminates and ferrites , Proc Fifth Inte-national Symposium on the Chemistry of Cement, Tokyo, 1968, 196-. pp 37-67; discussion by M. H...water-cement ratio contained ettringite, tetracalcium aluminate inonos-2;irate-12-hydrate, calcium hydroxide, calcium silicate hydrate gel, and

  3. Testing Urey's carbonate-silicate cycle using the calcium isotopic composition of sedimentary carbonates

    Science.gov (United States)

    Blättler, Clara L.; Higgins, John A.

    2017-12-01

    Carbonate minerals constitute a major component of the sedimentary geological record and an archive of a fraction of the carbon and calcium cycled through the Earth's surface reservoirs for over three billion years. For calcium, carbonate minerals constitute the ultimate sink for almost all calcium liberated during continental and submarine weathering of silicate minerals. This study presents >500 stable isotope ratios of calcium in Precambrian carbonate sediments, both limestones and dolomites, in an attempt to characterize the isotope mass balance of the sedimentary carbonate reservoir through time. The mean of the dataset is indistinguishable from estimates of the calcium isotope ratio of bulk silicate Earth, consistent with the Urey cycle being the dominant mechanism exchanging calcium among surface reservoirs. The variability in bulk sediment calcium isotope ratios within each geological unit does not reflect changes in the global calcium cycle, but rather highlights the importance of local mineralogical and/or diagenetic effects in the carbonate record. This dataset demonstrates the potential for calcium isotope ratios to help assess these local effects, such as the former presence of aragonite, even in rocks with a history of neomorphism and recrystallization. Additionally, 29 calcium isotope measurements are presented from ODP (Ocean Drilling Program) Site 801 that contribute to the characterization of altered oceanic crust as an additional sink for calcium, and whose distinct isotopic signature places a limit on the importance of this subduction flux over Earth history.

  4. Determine the compressive strength of calcium silicate bricks by combined nondestructive method.

    Science.gov (United States)

    Brozovsky, Jiri

    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 relationships are known for their close correlation and are applicable in practice. The highest correlation between parameters from nondestructive measurement and predicted compressive strength is obtained using the SonReb combined nondestructive method. Combined nondestructive SonReb method was proved applicable for determination of compressive strength of calcium silicate bricks at checking tests in a production plant and for evaluation of bricks built in existing masonry structures.

  5. 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.

  6. Hydration of calcium aluminate cement determined by thermal analysis

    Science.gov (United States)

    Scheinherrová, Lenka; Trník, Anton

    2017-07-01

    Calcium aluminate cements (CACs) are a very important type of non-Portland or special cements. Since they are considerably more expensive, they are not used as a simple substitute for Portland cement. Their structure allows them to achieve high compressive strength. They resist very well to high temperatures and temperature changes, or also to chemical attacks. The original motivation, why the CACs were developed, was the idea of finding new cement chemistries that would be more resistant to sulfate attack then Portland cements. Nowadays, the main usage of the CACs is in high temperatures applications. In this paper, we study the hydration of a CAC up to one year of age to control what happens in CACs structure during aging. The variety in the main products of hydration is studied using differential scanning calorimetry and thermogravimetry in the temperature range from 25 °C to 1000 °C with a heating rate of 5 °C/min in an argon atmosphere. The basic physical and mechanical properties are also determined.

  7. Aqueous solutions of calcium ions: hydration numbers and the effect of temperature.

    Science.gov (United States)

    Zavitsas, Andreas A

    2005-11-03

    Hydration numbers of calcium ions are determined from extensive measurements of colligative properties of water solutions of calcium salts. The hydration numbers reported refer to the average number of water molecules that are bound sufficiently strongly to calcium ions so as to be removed from the solvent and become part of the solute. Contrary to common descriptions of deviations from ideal behavior for concentrated solutions, ideal behavior is demonstrated when mole fractions are calculated by taking account of such bound water. Measurements over wide concentration and temperature ranges are used to obtain the effect of temperature on the average hydration number of Ca(2+). Freezing point depression measurements yield a hydration number of 12.0 +/- 0.8. Boiling point elevations yield 6.7 +/- 0.6. Consistent with this, vapor pressure measurements from 0 to 200 degrees C show a gradual decrease in hydration number with increasing temperature, with a value of 5.0 at 200 degrees C.

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

    Science.gov (United States)

    Marciano, Marina Angélica; Estrela, Carlos; Mondelli, Rafael Francisco Lia; Ordinola-Zapata, Ronald; Duarte, Marco Antonio Hungaro

    2013-01-01

    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 (pbismuth oxide was added showed radiopacity corresponding to the ISO recommendations (>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 (pbismuth oxide has no relation to the color alteration of calcium silicate-based cements.

  9. Porosity distribution in root canals filled with gutta percha and calcium silicate cement

    NARCIS (Netherlands)

    Moinzadeh, A.T.; Zerbst, W.; Boutsioukis, C.; Shemesh, H.; Zaslansky, P.

    2015-01-01

    Objective Gutta percha is commonly used in conjunction with a sealer to produce a fluid-tight seal within the root canal fillings. One of the most commonly used filling methods is lateral compaction of gutta percha coupled with a sealer such as calcium silicate cement. However, this technique may

  10. Calcium-silicate mesoporous nanoparticles loaded with chlorhexidine for both anti- Enterococcus faecalis and mineralization properties.

    Science.gov (United States)

    Fan, Wei; Li, Yanyun; Sun, Qing; Ma, Tengjiao; Fan, Bing

    2016-10-21

    In infected periapical tissues, Enterococcus faecalis is one of the most common dominant bacteria. Chlorhexidine has been proved to show strong antibacterial ability against E. faecalis but is ineffective in promoting mineralization for tissues around root apex. Mesoporous calcium-silicate nanoparticles are newly synthesized biomaterials with excellent ability to promote mineralization and carry-release bioactive molecules in a controlled manner. In this study, mesoporous calcium-silicate nanoparticles were functionalized with chlorhexidine and their releasing profile, antibacterial ability, effect on cell proliferation and in vitro mineralization property were evaluated. The chlorhexidine was successfully incorporated into mesoporous calcium-silicate nanoparticles by a mixing-coupling method. The new material could release chlorhexidine as well as Ca(2+) and SiO3(2-) in a sustained manner with an alkaline pH value under different conditions. The antimicrobial ability against planktonic E. faecalis was dramatically improved after chlorhexidine incorporation. The nanoparticles with chlorhexidine showed no negative effect on cell proliferation with low concentrations. On dentin slices, the new synthesized material demonstrated a similar inhibitory effect on E. faecalis as the chlorhexidine. After being immersed in SBF for 9 days, numerous apatite crystals could be observed on surfaces of the material tablets. Mesoporous calcium-silicate nanoparticles loaded with chlorhexidine exhibited release of ions and chlorhexidine, low cytotoxicity, excellent antibacterial ability and in vitro mineralization. This material could be developed into a new effective intra-canal medication in dentistry or a new bone defect filling material for infected bone defects.

  11. Synthesis of calcium silicates by Pechini method and exchanging ions of sodium alginate-calcium chloride

    Energy Technology Data Exchange (ETDEWEB)

    Flores-Garay, K.A.; Martinez-Luevanos, A.; Cruz-Ortiz, B.R.; Garcia-Cerda, L.A.; Lopez-Badillo, C.M.

    2016-07-01

    Calcium silicates samples were synthesized using tetraethyl orthosilicate (TEOS) and by Pechini methodology assisted with ion-exchange of sodium alginate, followed by a heat treatment of 800°C by two hours. A, B and C samples were obtained using 1.7×10−3M, 3.4×10−3M and 5.1×10−3M of TEOS, respectively, and without heat treatment; these samples were characterized by thermogravimetric analysis (TGA) and infrared spectroscopy with attenuated total reflectance (FTIR-ATR). Furthermore, samples A800, B800 and C800 obtained using a heat treatment of 800° by two hours were characterized by FTIR-ATR, absorption technique (BET), X-ray diffraction (XRD) and by scanning electron microscopy. The XRD patterns indicate that sample A800 contains olivine (Ca2SiO4) in orthorhombic phase and wollastonite-2M (CaSiO3); sample B800 showed the earlier phases and quartz (SiO2), whereas sample C800 contains wollastonite phases and larnite-2M (Ca2SiO4). (Author)

  12. Hydrated silicate minerals on Mars observed by the Mars Reconnaissance Orbiter CRISM instrument.

    Science.gov (United States)

    Mustard, John F; Murchie, S L; Pelkey, S M; Ehlmann, B L; Milliken, R E; Grant, J A; Bibring, J-P; Poulet, F; Bishop, J; Dobrea, E Noe; Roach, L; Seelos, F; Arvidson, R E; Wiseman, S; Green, R; Hash, C; Humm, D; Malaret, E; McGovern, J A; Seelos, K; Clancy, T; Clark, R; Marais, D D; Izenberg, N; Knudson, A; Langevin, Y; Martin, T; McGuire, P; Morris, R; Robinson, M; Roush, T; Smith, M; Swayze, G; Taylor, H; Titus, T; Wolff, M

    2008-07-17

    Phyllosilicates, a class of hydrous mineral first definitively identified on Mars by the OMEGA (Observatoire pour la Mineralogie, L'Eau, les Glaces et l'Activitié) instrument, preserve a record of the interaction of water with rocks on Mars. Global mapping showed that phyllosilicates are widespread but are apparently restricted to ancient terrains and a relatively narrow range of mineralogy (Fe/Mg and Al smectite clays). This was interpreted to indicate that phyllosilicate formation occurred during the Noachian (the earliest geological era of Mars), and that the conditions necessary for phyllosilicate formation (moderate to high pH and high water activity) were specific to surface environments during the earliest era of Mars's history. Here we report results from the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) of phyllosilicate-rich regions. We expand the diversity of phyllosilicate mineralogy with the identification of kaolinite, chlorite and illite or muscovite, and a new class of hydrated silicate (hydrated silica). We observe diverse Fe/Mg-OH phyllosilicates and find that smectites such as nontronite and saponite are the most common, but chlorites are also present in some locations. Stratigraphic relationships in the Nili Fossae region show olivine-rich materials overlying phyllosilicate-bearing units, indicating the cessation of aqueous alteration before emplacement of the olivine-bearing unit. Hundreds of detections of Fe/Mg phyllosilicate in rims, ejecta and central peaks of craters in the southern highland Noachian cratered terrain indicate excavation of altered crust from depth. We also find phyllosilicate in sedimentary deposits clearly laid by water. These results point to a rich diversity of Noachian environments conducive to habitability.

  13. Effect of Exposed Surface Area, Volume and Environmental pH on the Calcium Ion Release of Three Commercially Available Tricalcium Silicate Based Dental Cements

    Directory of Open Access Journals (Sweden)

    Sivaprakash Rajasekharan

    2018-01-01

    Full Text Available Tricalcium silicate cements (TSC are used in dental traumatology and endodontics for their bioactivity which is mostly attributed to formation of calcium hydroxide during TSC hydration and its subsequent release of calcium and hydroxide ions. The aim of this study was to determine the effect of volume (Vol, exposed surface area (ESA and pH of surrounding medium on calcium ion release. Three commercially available hydraulic alkaline dental cements were mixed and condensed into cylindrical tubes of varying length and diameter (n = 6/group. For the effect of ESA and Vol, tubes were immersed in 10 mL of deionized water. To analyze the effect of environmental pH, the tubes were randomly immersed in 10 mL of buffer solutions with varying pH (10.4, 7.4 or 4.4. The solutions were collected and renewed at various time intervals. pH and/or calcium ion release was measured using a pH glass electrode and atomic absorption spectrophotometer respectively. The change of pH, short-term calcium ion release and rate at which calcium ion release reaches maximum were dependent on ESA (p < 0.05 while maximum calcium ion release was dependent on Vol of TSC (p < 0.05. Maximum calcium ion release was significantly higher in acidic solution followed by neutral and alkaline solution (p < 0.05.

  14. Effect of Exposed Surface Area, Volume and Environmental pH on the Calcium Ion Release of Three Commercially Available Tricalcium Silicate Based Dental Cements.

    Science.gov (United States)

    Rajasekharan, Sivaprakash; Vercruysse, Chris; Martens, Luc; Verbeeck, Ronald

    2018-01-13

    Tricalcium silicate cements (TSC) are used in dental traumatology and endodontics for their bioactivity which is mostly attributed to formation of calcium hydroxide during TSC hydration and its subsequent release of calcium and hydroxide ions. The aim of this study was to determine the effect of volume (Vol), exposed surface area (ESA) and pH of surrounding medium on calcium ion release. Three commercially available hydraulic alkaline dental cements were mixed and condensed into cylindrical tubes of varying length and diameter ( n = 6/group). For the effect of ESA and Vol, tubes were immersed in 10 mL of deionized water. To analyze the effect of environmental pH, the tubes were randomly immersed in 10 mL of buffer solutions with varying pH (10.4, 7.4 or 4.4). The solutions were collected and renewed at various time intervals. pH and/or calcium ion release was measured using a pH glass electrode and atomic absorption spectrophotometer respectively. The change of pH, short-term calcium ion release and rate at which calcium ion release reaches maximum were dependent on ESA ( p < 0.05) while maximum calcium ion release was dependent on Vol of TSC ( p < 0.05). Maximum calcium ion release was significantly higher in acidic solution followed by neutral and alkaline solution ( p < 0.05).

  15. Pressure induced reactions amongst calcium aluminate hydrate phases

    KAUST Repository

    Moon, Ju-hyuk

    2011-06-01

    The compressibilities of two AFm phases (strätlingite and calcium hemicarboaluminate hydrate) and hydrogarnet were obtained up to 5 GPa by using synchrotron high-pressure X-ray powder diffraction with a diamond anvil cell. The AFm phases show abrupt volume contraction regardless of the molecular size of the pressure-transmitting media. This volume discontinuity could be associated to a structural transition or to the movement of the weakly bound interlayer water molecules in the AFm structure. The experimental results seem to indicate that the pressure-induced dehydration is the dominant mechanism especially with hygroscopic pressure medium. The Birch-Murnaghan equation of state was used to compute the bulk modulus of the minerals. Due to the discontinuity in the pressure-volume diagram, a two stage bulk modulus of each AFm phase was calculated. The abnormal volume compressibility for the AFm phases caused a significant change to their bulk modulus. The reliability of this experiment is verified by comparing the bulk modulus of hydrogarnet with previous studies. © 2011 Elsevier Ltd. All rights reserved.

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

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    Cinthya Souza Santana

    2016-01-01

    Full Text Available 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, 800 and 1,000 kg/ha and the subplots were the two cutting seasons (rainy and dry period, with five repetitions (blocks. The calcium and magnesium silicate doses exerted no significant effect on green or dry matter production, chemical forage composition or degradability parameters. On the other hand, there was an effect of cutting period on forage production and chemical composition. The highest production of green and dry matter was observed during the rainy period, while acid detergent fiber content was higher during the dry season. The treatments did not exert any significant effect on the parameters of degradability that would alter the nutritive value of bluestem grass.

  17. 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.

  18. Hydration mechanisms of mineral trioxide aggregate.

    Science.gov (United States)

    Camilleri, J

    2007-06-01

    To report the hydration mechanism of white mineral trioxide aggregate (White MTA, Dentsply, Tulsa Dental Products, Tulsa, OK, USA). The chemical constitution of white MTA was studied by viewing the powder in polished sections under the scanning electron microscope (SEM). The hydration of both white MTA and white Portland cement (PC) was studied by characterizing cement hydrates viewed under the SEM, plotting atomic ratios, performing quantitative energy dispersive analyses with X-ray (EDAX) and by calculation of the amount of anhydrous clinker minerals using the Bogue calculation. Un-hydrated MTA was composed of impure tri-calcium and di-calcium silicate and bismuth oxide. The aluminate phase was scarce. On hydration the white PC produced a dense structure made up of calcium silicate hydrate, calcium hydroxide, monosulphate and ettringite as the main hydration products. The un-reacted cement grain was coated with a layer of hydrated cement. In contrast MTA produced a porous structure on hydration. Levels of ettringite and monosulphate were low. Bismuth oxide was present as un-reacted powder but also incorporated with the calcium silicate hydrate. White MTA was deficient in alumina suggesting that the material was not prepared in a rotary kiln. On hydration this affected the production of ettringite and monosulphate usually formed on hydration of PC. The bismuth affected the hydration mechanism of MTA; it formed part of the structure of C-S-H and also affected the precipitation of calcium hydroxide in the hydrated paste. The microstructure of hydrated MTA would likely be weaker when compared with that of PC.

  19. Fluorescent properties of a green- to red-emitting Eu{sup 3+}, Tb{sup 3+} codoped amorphous calcium silicate phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Kojima, Yoshiyuki, E-mail: ykojima@chem.cst.nihon-u.ac.jp [Department of Materials and Applied Chemistry, Faculty of Science and Engineering, Nihon University, 1-8, Kanda-Surugadai, Chiyoda-ku, Tokyo 101-8308 (Japan); Numazawa, Masaaki; Umegaki, Tetsuo [Department of Materials and Applied Chemistry, Faculty of Science and Engineering, Nihon University, 1-8, Kanda-Surugadai, Chiyoda-ku, Tokyo 101-8308 (Japan)

    2012-10-15

    A Eu{sup 3+}, Tb{sup 3+} codoped amorphous calcium silicate phosphor was prepared by heating a Eu{sup 3+}, Tb{sup 3+} codoped calcium silicate hydrate phosphor formed by liquid-phase reaction for 30 min at 900 Degree-Sign C. The excitation peak wavelength of the resulting phosphor was 379 nm and the emission peak wavelengths were at 542 nm, attributed to the {sup 5}D{sub 4}{yields}{sup 7}F{sub 5} transition of Tb{sup 3+}, and at 613 mm, attributed to the {sup 5}D{sub 0}{yields}{sup 7}F{sub 1} transition of Eu{sup 3+}. The intensity ratio of the two peaks could be freely controlled by varying the Eu/Tb atomic ratio of the Eu{sup 3+}, Tb{sup 3+} 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 Tb{sup 3+} to Eu{sup 3+} is occurring. - Highlights: Black-Right-Pointing-Pointer A Eu{sup 3+}, Tb{sup 3+} codoped CSH phosphor was synthesized by liquid-phase reaction. Black-Right-Pointing-Pointer CSH phosphor was heated at 900 Degree-Sign C to obtain Eu{sup 3+}, Tb{sup 3+} codoped amorphous calcium silicate phosphor. Black-Right-Pointing-Pointer Under 379 nm excitation, this phosphor showed emission peaks at 542 nm and 613 nm. Black-Right-Pointing-Pointer The luminescent color could be continuously changed from green to red with increasing Eu/Tb atomic ratio. Black-Right-Pointing-Pointer It was clarified that electron transfer from Tb{sup 3+} to Eu{sup 3+} is occurring.

  20. Calcium aluminate cement hydration in a high alkalinity environment

    Directory of Open Access Journals (Sweden)

    Palomo, Á.

    2009-03-01

    Full Text Available The present paper forms part of a broader research project that aims primarily to devise new cementitious products via the alkali activation of silico-aluminous materials. This work addresses the possibility of using small percentages of calcium aluminate cement (CAC as a source of reactive aluminium. For this reason, a preliminary review was needed of the behaviour of CACs in highly alkaline media (2, 8 and 12M NaOH solutions. Two, 28- and 180-day mechanical strength was determined and the reaction products were characterized with XRD and FTIR. The water-hydrated CAC was used as the control.The results obtained showed that CAC hardening took place much more slowly in highly alkaline media than in water. Nonetheless, the 28-day compressive strength obtained, ≥80MPa. As main reaction products, to ambient temperature and from the two days of cured, cubic aluminate C3AH6, and AH3 polymorphs are formed, instead of the usual hexagonal aluminatos (CAH10 and C2AH8 that are formed in the normal hydrate with water.El presente trabajo forma parte de una amplia investigación cuyo objetivo principal es el de elaborar nuevos materiales con propiedades cementantes mediante la activación alcalina de materiales de naturaleza silito-aluminosa. En estos estudios se contempla la posibilidad de utilizar pequeños porcentajes de cemento de aluminato de calcio (CAC como fuente de aluminio reactivo. Por ello inicialmente se ha estudiado el comportamiento de los CAC en medios fuertemente alcalinos (disoluciones de NaOH 2M, 8M y 12M. Se determinaron las resistencias mecánicas a 2, 28 y 180 días y se realizó una caracterización de los productos de reacción formados por DRX, FTIR. Como sistema de referencia se consideró la hidratación del CAC con agua.Los resultados obtenidos muestran que en medios fuertemente alcalinos se retrasan los procesos de rápido endurecimiento de CAC con agua. No obstante a 28 días se obtienen valores de resistencia a compresión

  1. 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.

  2. Incorporation of bitumen and calcium silicate in cement and lime stabilized soil blocks

    Science.gov (United States)

    Kwan, W. H.; Cheah, C. B.; Ramli, M.; Al-Sakkaf, Y. K.

    2017-04-01

    Providing affordable housing is the most critical problem in many of the developing countries. Using earth materials in building construction is one of the feasible methods to address this issue and it can be a way towards sustainable construction as well. However, the published information on the stabilized soil blocks is limited. Therefore, the present study is conducted to examine the characterization of the soils and engineering properties of the stabilized soil blocks. Four types of stabilizer were used in the study, namely; cement, slaked lime, bitumen emulsion and calcium silicate. Cement and slaked lime were added at different percentages in the range of 5% to 15%, with interval of 2.5%. The percentage was determined based on weight of soil. Meanwhile, bitumen emulsion and calcium silicate were incorporated at various percentages together with 10% of cement. Dosage of bitumen emulsion is in the range of 2% to 10% at interval of 2% while calcium silicate was incorporated at 0.50%, 0.75%, 1.00%, 1.25%, 1.50% and 2.00%. Results show that cement is the most viable stabilizer for the soil block among all stabilizers in this study. The bulk density, optimum moisture content and compressive strengths were increased with the increasing cement content. The most suitable cement content was 10% added at moisture content of 12%. Lime, bitumen and calcium contents were recommended at 5.0%, 6.0% and 1.25%, respectively.

  3. Identification of the hydrate gel phases present in phosphate-modified calcium aluminate binders

    Energy Technology Data Exchange (ETDEWEB)

    Chavda, Mehul A.; Bernal, Susan A. [Department of Materials Science and Engineering, The University of Sheffield, Sheffield S1 3JD (United Kingdom); Apperley, David C. [Solid-State NMR Group, Department of Chemistry, Durham University, Durham DH1 3LE (United Kingdom); Kinoshita, Hajime [Department of Materials Science and Engineering, The University of Sheffield, Sheffield S1 3JD (United Kingdom); Provis, John L., E-mail: j.provis@sheffield.ac.uk [Department of Materials Science and Engineering, The University of Sheffield, Sheffield S1 3JD (United Kingdom)

    2015-04-15

    The conversion of hexagonal calcium aluminate hydrates to cubic phases in hydrated calcium aluminate cements (CAC) can involve undesirable porosity changes and loss of strength. Modification of CAC by phosphate addition avoids conversion, by altering the nature of the reaction products, yielding a stable amorphous gel instead of the usual crystalline hydrate products. Here, details of the environments of aluminium and phosphorus in this gel were elucidated using solid-state NMR and complementary techniques. Aluminium is identified in both octahedral and tetrahedral coordination states, and phosphorus is present in hydrous environments with varying, but mostly low, degrees of crosslinking. A {sup 31}P/{sup 27}Al rotational echo adiabatic passage double resonance (REAPDOR) experiment showed the existence of aluminium–phosphorus interactions, confirming the formation of a hydrated calcium aluminophosphate gel as a key component of the binding phase. This resolves previous disagreements in the literature regarding the nature of the disordered products forming in this system.

  4. Correlative micro-Raman/EPMA analysis of the hydraulic calcium silicate cement interface with dentin.

    Science.gov (United States)

    Li, Xin; Pongprueksa, Pong; Van Landuyt, Kirsten; Chen, Zhi; Pedano, Mariano; Van Meerbeek, Bart; De Munck, Jan

    2016-09-01

    This study aims to characterize the chemical interplay of hydraulic calcium silicate cements at dentin. Class I cavities were prepared in non-carious human third molars and filled with Biodentine (Septodont) or ProRoot MTA (Dentsply). After 1-day, 1-week, and 1-month Dulbecco's phosphate-buffered saline (DPBS) storage, the specimens were cross-sectioned perpendicular to the cement-dentin interface. The interfaces were evaluated using micro-Raman (μRaman) spectroscopy and at a higher spatial resolution using field emission gun electron probe microanalysis (Feg-SEM/EPMA). μRaman spectroscopy revealed the formation of a transition zone at the interface of both Biodentine (Septodont) and ProRoot MTA (Dentsply) with dentin, having an average thickness of, respectively, 7.5 ± 4.2 and 6.2 ± 5.4 μm, which however was not statistically different. No difference in interfacial ultrastructure and chemistry was found using μRaman spectroscopy between 1 day, 1 week, and 1 month DPBS-stored specimens. The observation of a transition zone at the cement-dentin interfaces contrasts with the EPMA data that revealed a sharper transition from cement to dentin. Again, no difference in interfacial ultrastructure and chemistry was found for different storage periods, with the exception of one 1 month DPBS-stored specimen prepared using Biodentine (Septodont). More specifically, EPMA revealed a gap of about 10-μm wide in the latter specimen that was filled up with newly formed calcium phosphate depositions. Up to 1 month, the interaction of hydraulic calcium silicate cements investigated did not reveal ultrastructural or chemical changes at unaffected dentin with the exception of a calcium phosphate gap-filling property. Hydraulic calcium silicate cements were found to fill gaps by calcium phosphate deposition, however, without conducting chemical changes to the adjacent dentin.

  5. The effect of pressure on tricalcium silicate hydration at different temperatures and in the presence of retarding additives

    Energy Technology Data Exchange (ETDEWEB)

    Jupe, Andrew C.; Wilkinson, Angus P.; Funkhouser, Gary P. (Halliburton); (GIT)

    2012-07-25

    The hydration of tricalcium silicate (C{sub 3}S) is accelerated by pressure. However, the extent to which temperature and/or cement additives modify this effect is largely unknown. Time-resolved synchrotron powder diffraction has been used to study cement hydration as a function of pressure at different temperatures in the absence of additives, and at selected temperatures in the presence of retarding agents. The magnitudes of the apparent activation volumes for C{sub 3}S hydration increased with the addition of the retarders sucrose, maltodextrin, aminotri(methylenephosphonic acid) and an AMPS copolymer. Pressure was found to retard the formation of Jaffeite relative to the degree of C{sub 3}S hydration in high temperature experiments. For one cement slurry studied without additives, the apparent activation volume for C{sub 3}S hydration remained close to {approx} -28 cm{sup 3} mol{sup -1} over the range 25 to 60 C. For another slurry, there were possible signs of a decrease in magnitude at the lowest temperature examined.

  6. Formation of low-T hydrated silicates in modern microbialites from Mexico and implications for microbial fossilization

    Directory of Open Access Journals (Sweden)

    Nina eZeyen

    2015-10-01

    Full Text Available Microbialites are organo-sedimentary rocks found in abundance throughout the geological record back to ~3.5 Ga. Interpretations of the biological and environmental conditions under which they formed rely on comparisons with modern microbialites. Therefore, a better characterization of diverse modern microbialites is crucial to improve such interpretations. Here, we studied modern microbialites from three Mexican alkaline crater lakes: Quechulac, La Preciosa and Atexcac. The geochemical analyses of water solutions showed that they were supersaturated to varying extents with several mineral phases, including aragonite, calcite, hydromagnesite, as well as hydrated Mg-silicates. Consistently, X-ray diffraction and Fourier transform infrared spectroscopy analyses revealed that microbialites are composed of a diversity of mineral phases including aragonite and sometimes calcite, hydromagnesite, and more interestingly, a poorly-crystalline hydrated silicate phase. Coupling of scanning electron microscopy with energy dispersive X-ray spectrometry microanalyses on polished sections showed that this latter phase is abundant, authigenic, magnesium-rich and sometimes associated with iron and manganese. This mineral phase is similar to kerolite, a hydrated poorly crystalline talc-like phase (Mg3Si4O10(OH2·nH2O. Diverse microfossils were permineralized by this silicate phase. Some of them were imaged in 3D by FIB-tomography showing that their morphologically was exquisitely preserved down to the few nm-scale. The structural and chemical features of these fossils were further studied using a combination of transmission electron microscopy and scanning transmission X-ray microscopy at the carbon and magnesium K-edges and iron L2,3-edges. These results showed that organic carbon is pervasively associated with kerolite. Overall, it is suggested that the poorly-crystalline hydrated magnesium-rich silicate forms in many alkaline lakes and has a strong potential

  7. Formation of low-T hydrated silicates in modern microbialites from Mexico and implications for microbial fossilization

    Science.gov (United States)

    Zeyen, Nina; Benzerara, Karim; Li, Jinhua; Groleau, Alexis; Balan, Etienne; Robert, Jean-Louis; Esteve, Imene; Tavera, Rosaluz; Moreira, David; Lopez-Garcia, Purificacion

    2015-10-01

    Microbialites are organo-sedimentary rocks found in abundance throughout the geological record back to ~3.5 Ga. Interpretations of the biological and environmental conditions under which they formed rely on comparisons with modern microbialites. Therefore, a better characterization of diverse modern microbialites is crucial to improve such interpretations. Here, we studied modern microbialites from three Mexican alkaline crater lakes: Quechulac, La Preciosa and Atexcac. The geochemical analyses of water solutions showed that they were supersaturated to varying extents with several mineral phases, including aragonite, calcite, hydromagnesite, as well as hydrated Mg-silicates. Consistently, X-ray diffraction and Fourier transform infrared spectroscopy analyses revealed that microbialites are composed of a diversity of mineral phases including aragonite and sometimes calcite, hydromagnesite, and more interestingly, a poorly-crystalline hydrated silicate phase. Coupling of scanning electron microscopy with energy dispersive X-ray spectrometry microanalyses on polished sections showed that this latter phase is abundant, authigenic, magnesium-rich and sometimes associated with iron and manganese. This mineral phase is similar to kerolite, a hydrated poorly crystalline talc-like phase (Mg3Si4O10(OH)2·nH2O). Diverse microfossils were permineralized by this silicate phase. Some of them were imaged in 3D by FIB-tomography showing that their morphologically was exquisitely preserved down to the few nm-scale. The structural and chemical features of these fossils were further studied using a combination of transmission electron microscopy and scanning transmission X-ray microscopy at the carbon and magnesium K-edges and iron L2,3-edges. These results showed that organic carbon is pervasively associated with kerolite. Overall, it is suggested that the poorly-crystalline hydrated magnesium-rich silicate forms in many alkaline lakes and has a strong potential for fossilization of

  8. 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.

  9. 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.

  10. 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.

  11. PENGARUH PENAMBAHAN SURFAKTAN SODIUM LIGNOSULFONAT (SLS) DALAM PROSES PENGENDAPAN NANO CALCIUM SILICATE (NCS) DARI GEOTHERMAL BRINE

    OpenAIRE

    Ulya, M Ridho; Perdana, Indra; Mulyono, Panut

    2018-01-01

    Konsentrasi yang tinggi dari kelarutan silika dalam larutan geothermal menyebabkan masalah dalam pengoperasian produksi uap di PLTP Dieng. Mitigasi silika scaling diperlukan untuk mengurangi resiko kegagalan produksi uap. Dalam penelitian ini, asam silika dalam larutan geothermal direaksikan dengan kalsium hidroksida (Ca(OH)2) membentuk n ano calcium silicate (NCS). Tujuan penelitian ini adalah membentuk endapan NCS dari surfaktan SLS dan Ca(OH)2 ke dalam larutan geothermal. Mempelajari perub...

  12. 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.

  13. Rapid hydrothermal flow synthesis and characterisation of carbonate- and silicate-substituted calcium phosphates.

    Science.gov (United States)

    Chaudhry, Aqif A; Knowles, Jonathan C; Rehman, Ihtesham; Darr, Jawwad A

    2013-09-01

    A range of crystalline and nano-sized carbonate- and silicate-substituted hydroxyapatite has been successfully produced by using continuous hydrothermal flow synthesis technology. Ion-substituted calcium phosphates are better candidates for bone replacement applications (due to improved bioactivity) as compared to phase-pure hydroxyapatite. Urea was used as a carbonate source for synthesising phase pure carbonated hydroxyapatite (CO₃-HA) with ≈5 wt% substituted carbonate content (sample 7.5CO₃-HA) and it was found that a further increase in urea concentration in solution resulted in biphasic mixtures of carbonate-substituted hydroxyapatite and calcium carbonate. Transmission electron microscopy images revealed that the particle size of hydroxyapatite decreased with increasing urea concentration. Energy-dispersive X-ray spectroscopy result revealed a calcium deficient apatite with Ca:P molar ratio of 1.45 (±0.04) in sample 7.5CO₃-HA. For silicate-substituted hydroxyapatite (SiO₄-HA) silicon acetate was used as a silicate ion source. It was observed that a substitution threshold of ∼1.1 wt% exists for synthesis of SiO₄-HA in the continuous hydrothermal flow synthesis system, which could be due to the decreasing yields with progressive increase in silicon acetate concentration. All the as-precipitated powders (without any additional heat treatments) were analysed using techniques including Transmission electron microscopy, X-ray powder diffraction, Differential scanning calorimetry, Thermogravimetric analysis, Raman spectroscopy and Fourier transform infrared spectroscopy.

  14. NON-AUTOCLAVE SILICATE BRICK

    Directory of Open Access Journals (Sweden)

    V. N. Yaglov

    2015-01-01

    Full Text Available The paper proposes a technology for obtaining bricks on the basis of lime-silica mixtures where chemical interactions are practically completely realized in dispersive state at the stage of preparation of binding contact maturing and raw mixture as a whole. The role of forming operation (moulding is changed in principle because in this case conversion of dispersive system into a rock-like solid occurs and due to this the solid obtains complete water-resistance in contact with water immediately after forming operation. Theoretical basis for the developed technology is capability of silicate dispersive substances (hydrated calcium silicate to transit in non-stable state, to form a rock-like water-resistant solid in the moment of mechanical load application during forming process. Specific feature of the proposed method is an exclusion of additional operations for autoclaving of products from the process of obtaining a silicate brick.Synthetic hydrated calcium silicate in contrast to natural ones are more uniform in composition and structure, they contain less impurities and they are characterized by dispersive composition and due to the mentioned advantages they find wider practical application. Contact-condensation binders permit to manipulate product properties on their basis and ensure maximum correspondence to the requirements of the concrete application. Raw material sources for obtaining synthetic hydrated calcium silicates are practically un-limited because calcium-silicon containing substances are found as in various technogenic wastes so in natural compounds as well. So the problem for obtaining hydrated calcium silicates having contact-condensation ability for structure formation becomes more and more actual one. This transition is considered as dependent principally on arrangement rate of substance particles which determined the level of its instability.

  15. Chemical characteristics of mineral trioxide aggregate and its hydration reaction

    Science.gov (United States)

    2012-01-01

    Mineral trioxide aggregate (MTA) was developed in early 1990s and has been successfully used for root perforation repair, root end filling, and one-visit apexification. MTA is composed mainly of tricalcium silicate and dicalcium silicate. When MTA is hydrated, calcium silicate hydrate (CSH) and calcium hydroxide is formed. Formed calcium hydroxide interacts with the phosphate ion in body fluid and form amorphous calcium phosphate (ACP) which finally transforms into calcium deficient hydroxyapatite (CDHA). These mineral precipitate were reported to form the MTA-dentin interfacial layer which enhances the sealing ability of MTA. Clinically, the use of zinc oxide euginol (ZOE) based materials may retard the setting of MTA. Also, the use of acids or contact with excessive blood should be avoided before complete set of MTA, because these conditions could adversely affect the hydration reaction of MTA. Further studies on the chemical nature of MTA hydration reaction are needed. PMID:23429542

  16. Chemical characteristics of mineral trioxide aggregate and its hydration reaction.

    Science.gov (United States)

    Chang, Seok-Woo

    2012-11-01

    Mineral trioxide aggregate (MTA) was developed in early 1990s and has been successfully used for root perforation repair, root end filling, and one-visit apexification. MTA is composed mainly of tricalcium silicate and dicalcium silicate. When MTA is hydrated, calcium silicate hydrate (CSH) and calcium hydroxide is formed. Formed calcium hydroxide interacts with the phosphate ion in body fluid and form amorphous calcium phosphate (ACP) which finally transforms into calcium deficient hydroxyapatite (CDHA). These mineral precipitate were reported to form the MTA-dentin interfacial layer which enhances the sealing ability of MTA. Clinically, the use of zinc oxide euginol (ZOE) based materials may retard the setting of MTA. Also, the use of acids or contact with excessive blood should be avoided before complete set of MTA, because these conditions could adversely affect the hydration reaction of MTA. Further studies on the chemical nature of MTA hydration reaction are needed.

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

    Science.gov (United States)

    Nagas, Emre; Cehreli, Zafer; Uyanik, Mehmet Ozgur; Durmaz, Veli

    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 calcium silicate-based sealer + gutta-percha; (3) a calcium silicate-based sealer + Resilon; (4) a methacrylate resin-based sealer (RealSeal SE) + Resilon; (5) an epoxy resin-based sealer (AH Plus) + gutta-percha, and (6) a mineral trioxide aggregate-based endodontic sealer (MTA Fillapex) + gutta-percha. Four 1-mm-thick sections were obtained from the coronal aspect of each root (n = 40 slices/group). Push-out bond strength testing was performed at a cross-head speed of 1 mm/min, and the bond strength data were analyzed statistically by one-way analysis of variance and Tukey tests (p core filling materials. When the calcium silicate-based sealer was placed in bulk, its dislocation resistance was similar to that of commonly used sealer + core root filling systems. Thus, the concept of using a calcium silicate-based sealer in bulk can be more easily advocated in clinical practice.

  18. 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

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

    DEFF Research Database (Denmark)

    Moesgaard, M; Poulsen, Søren Lundsted; Herfort, D

    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)....

  20. The Effect of Synthetic Hydrated Calcium Aluminate Additive on the Hydration Properties of OPC

    OpenAIRE

    Jolanta Doneliene; Anatolijus Eisinas; Kestutis Baltakys; Agne Bankauskaite

    2016-01-01

    The effect of synthetic CAH (130°C; 8 h; CaO/(SiO2 + Al2O3) = 0.55; Al2O3/(SiO2 + Al2O3) = 0.1, 0.15) with different crystallinity on the hydration kinetics of OPC at early stages of hydration was investigated. Also, the formation mechanism of compounds during OPC hydration was highlighted. It was determined that the synthetic CAH accelerated the initial reaction and shortened the induction period. Also, the second and third exothermic reactions begun earlier, and, during the latter reaction,...

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

    Directory of Open Access Journals (Sweden)

    Geraldo R. Zuba Junio

    2015-11-01

    Full Text Available 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, 47.62 and 71.43 t ha-1, on dry basis. Soil organic matter (OM, pH, sum of bases (SB, effective cation exchange capacity (CEC(t, total cation exchange capacity (CEC(T, base saturation (V% and potential acidity (H + Al were evaluated. There were no significant interactions between doses of sewage sludge compost and doses of Ca-Mg silicate on soil attributes, and no effect of silicate fertilization on these attributes. However, fertilization with sewage sludge compost promoted reduction in pH and increase in H + Al, OM and CEC. The dose of 71.43 t ha-1 of sewage sludge compost promoted the best soil chemical conditions.

  2. Effect of chemical environment on the dynamics of water confined in calcium silicate minerals: natural and synthetic tobermorite.

    Science.gov (United States)

    Monasterio, Manuel; Gaitero, Juan J; Manzano, Hegoi; Dolado, Jorge S; Cerveny, Silvina

    2015-05-05

    Confined water in the slit mesopores of the mineral tobermorite provides an excellent model system for analyzing the dynamic properties of water confined in cement-like materials. In this work, we use broadband dielectric spectroscopy (BDS) to analyze the dynamic of water entrapped in this crystalline material. Two samples, one natural and one synthetic, were analyzed, and despite their similar structure, the motion of confined water in their zeolitic cavity displays considerably different behavior. The water dynamics splits into two different behaviors depending on the chemical nature of the otherwise identical structural environment: water molecules located in areas where the primary building units are SiO4 relax slowly compared to water molecules located in cavities built with both AlO4 and SiO4. Compared to water confined in regular porous systems, water restricted in tobermorite is slower, indicating that the mesopore structure induces high disorder in the water structure. A comparison with water confined in the C-S-H gel is also discussed in this work. The strong dynamical changes in water due to the presence of aluminum might have important implications in the chemical transport of ions within hydrated calcium silicates, a process that governs the leaching and chemical degradation of cement.

  3. Hydrate Phase Assemblages in Calcium Sulfoaluminate - Metakaolin - Limestone Blends

    DEFF Research Database (Denmark)

    Pedersen, Malene Thostrup; Lothenbach, Barbara; Winnefeld, Frank

    2017-01-01

    as 27Al and 29Si NMR and compared with predictions from thermodynamic modelling. The results show almost full degrees of reaction for ye’elimite in all blends and that the degrees of reaction for belite and MK have an important impact on the hydrate phases and their quantities formed in the ternary...... systems....

  4. Hydration Characteristics of Tetracalcium Alumino-Ferrite Phase in the presence Calcium Carbonate

    Directory of Open Access Journals (Sweden)

    M. M. Radwan

    2011-12-01

    Full Text Available Tetracalcium alumino-ferrite phase (C4AF prepared from pure starting materials was employed for composing various mixes prepared of C4AF phase, CaSO4·2H2O, Ca(OH2 and CaCO3. The effect of replacing calcium sulphate (gypsum by calcium carbonate as a set retarder on the hydration behaviour of ferrite phase was studied. The mixes were hydrated for various periods and the hydration products were investigated using the appropriate techniques. The kinetics of hydration was studied by measuring the chemically-combined water as well as the combined lime contents. The mineralogical constitution was studied by using XRD, and DTA. The microstructure of some represented hydrated samples was investigated by scanning electron microscopy. Some interesting conclusions have been drawn. It was found that calcium carbonate reacts with tetracalcium alumino-ferrite phase (C4AF in the presence of hydrolime [Ca(OH2] to form carboferrite compounds which may coat the aluminate grains as ettringite does and this may probably regulate the setting time.

  5. Dentine-pulp tissue engineering in miniature swine teeth by set calcium silicate containing bioactive molecules.

    Science.gov (United States)

    Tziafas, Dimitrios; Kodonas, Konstantinos; Gogos, Christos; Tziafa, Christina; Papadimitriou, Seraphim

    2017-01-01

    The present study aims to investigate whether reparative dentinogenesis could be guided at central pulpal sites or at a distance from the amputated pulp of miniature pig teeth, by using set calcium silicate-based carriers containing human recombinant bioactive molecules. Pulp exposures were performed in 72 permanent teeth of 4 healthy miniature swine. The teeth were capped with pre-manufactured implants of set calcium silicate-based material containing BMP-7, TGFβ1 or WnT-1, for 3 weeks. Conical-shaped intrapulpal implants were exposed in the central pulp core, while disc-shaped extrapulpal implants were placed at a distance from the amputated pulp. Implants without bioactive molecules were used as controls. Thickness and forms of new matrix mineralized deposition were assessed histologically at post-operative periods of 3 weeks by light microscopy. Intrapulpal applications: Calcified structures composed of osteodentine were found in contact with the BMP-7 implants. An inhomogeneous calcified tissue matrix was found around the WnT-1 carriers. A two-zone calcified structure composed of osteodentine and a thicker tubular matrix zone was seen at the TGFβ1 carrier-pulp interface. Extrapulpal applications: The space between WnT-1 implants and pulp periphery had been invaded by soft tissue with traces of calcified foci. Thick calcified structures composed of osteodentine were found surrounding pulp exposure sites in response to application of BMP-7. Spindle-shaped cells associated with atubular calcified matrix or elongated polarized cells associated with tubular dentine-like matrix were found along the cut dentinal walls of the TGFβ1 group. The present experiments indicated that set calcium silicate could be used as carrier for biologically active molecules. TGFβ1 was shown to be an effective bioactive molecule in guiding tertiary dentine formation. Copyright © 2016 Elsevier Ltd. All rights reserved.

  6. 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

  7. Rapid hydrothermal flow synthesis and characterisation of carbonate- and silicate-substituted calcium phosphates

    Science.gov (United States)

    Knowles, Jonathan C; Rehman, Ihtesham; Darr, Jawwad A

    2013-01-01

    A range of crystalline and nano-sized carbonate- and silicate-substituted hydroxyapatite has been successfully produced by using continuous hydrothermal flow synthesis technology. Ion-substituted calcium phosphates are better candidates for bone replacement applications (due to improved bioactivity) as compared to phase-pure hydroxyapatite. Urea was used as a carbonate source for synthesising phase pure carbonated hydroxyapatite (CO3-HA) with ≈5 wt% substituted carbonate content (sample 7.5CO3-HA) and it was found that a further increase in urea concentration in solution resulted in biphasic mixtures of carbonate-substituted hydroxyapatite and calcium carbonate. Transmission electron microscopy images revealed that the particle size of hydroxyapatite decreased with increasing urea concentration. Energy-dispersive X-ray spectroscopy result revealed a calcium deficient apatite with Ca:P molar ratio of 1.45 (±0.04) in sample 7.5CO3-HA. For silicate-substituted hydroxyapatite (SiO4-HA) silicon acetate was used as a silicate ion source. It was observed that a substitution threshold of ∼1.1 wt% exists for synthesis of SiO4-HA in the continuous hydrothermal flow synthesis system, which could be due to the decreasing yields with progressive increase in silicon acetate concentration. All the as-precipitated powders (without any additional heat treatments) were analysed using techniques including Transmission electron microscopy, X-ray powder diffraction, Differential scanning calorimetry, Thermogravimetric analysis, Raman spectroscopy and Fourier transform infrared spectroscopy. PMID:22983020

  8. 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.

  9. Hydrate sodium calcium aluminosilicate does not reduce rumen lipopolysacharide concentrations in cows

    NARCIS (Netherlands)

    Pilachai, R.; Schonewille, J.T.; Thamrongyoswittayakul, C.; Aiumlamai, S.; Wachirapakorn, C.; Everts, H.; Vlaeminck, B.; Doekes, G.; Hendriks, W.H.

    2014-01-01

    The efficacy of hydrate sodium calcium aluminosilicate (HSCAS) to reduce the concentrations of free lipopolysaccharide (LPS) in rumen fluid of cows was investigated. Six, rumen-fistulated crossbred Holstein, non-pregnant, dry cows were randomly assigned to three experimental rations in a study with

  10. 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.

  11. Environmental scanning electron microscopy connected with energy dispersive x-ray analysis and Raman techniques to study ProRoot mineral trioxide aggregate and calcium silicate cements in wet conditions and in real time.

    Science.gov (United States)

    Gandolfi, Maria Giovanna; Van Landuyt, Kirsten; Taddei, Paola; Modena, Enrico; Van Meerbeek, Bart; Prati, Carlo

    2010-05-01

    ProRoot mineral trioxide aggregate (MTA) and calcium silicate cements are able to set in a moist environment. The aim of the study was to examine the surface structure and composition of a cement paste under wet conditions and in real time during setting by environmental scanning electron microscopy connected with energy dispersive x-ray analysis (ESEM-EDX) and micro-Raman techniques. White ProRoot MTA and experimental white tetrasilicate cement (wTC) and wTC containing bismuth oxide (wTC-Bi) were studied. Cement disks were analyzed 10 minutes after powder-liquid mixing (freshly prepared samples) and after immersion in Dulbecco phosphate-buffered saline at 37 degrees C for 24 hours (24-hour-aged samples). Freshly prepared wet cements at ESEM-EDX exposed an irregular surface (displaying calcium, silicon, aluminum, chlorine reflexes, and bismuth traces in MTA and wTC-Bi) with needle-like and cubic-hexagonal shaped crystals. Aggregates of spheroidal Ca-P-rich crystals (spherulites) appeared on the surface of 24-hour-aged samples. The starting unhydrated powders displayed the typical Raman bands of Portland cement components: alite, belite, and calcium sulfate (only as anhydrite in MTA and as both anhydrite and gypsum in wTC and wTC-Bi). MTA powder showed higher amount of calcium carbonate and lower quantities of anhydrite and higher crystallinity of the silicate component, leading to a slower hydration reaction. Products/markers of hydration reactions were present on fresh samples; ettringite formed on the surface of all the cements; calcium hydroxide (portlandite) was detected only on the surface of wTC, but no conclusion can be drawn on wTC-Bi and MTA because of the interference of bismuth oxide. Calcium phosphate and calcite/aragonite bands were detected on all 24-hour-aged cements; portlandite was no longer detected on wTC. ESEM and micro-Raman are powerful and suitable techniques to investigate endodontic calcium silicate hydrated cements in real time and in

  12. Microstructure and mechanical properties of stainless steel/calcium silicate composites manufactured by selective laser melting.

    Science.gov (United States)

    Zheng, Zeng; Wang, Lianfeng; Jia, Min; Cheng, Lingyu; Yan, Biao

    2017-02-01

    Selective laser melting (SLM) is raised as one kind of additive manufacturing (AM) which is based on the discrete-stacking concept. This technique can fabricate advanced composites with desirable properties directly from 3D CAD data. In this research, 316L stainless steel (316L SS) and different fractions of calcium silicate (CaSiO3) composites (weight fractions of calcium silicate are 0%, 5%,10% and 15%, respectively) were prepared by SLM technique with a purpose to develop biomedical metallic materials. The relative density, tensile, microhardness and elastic modulus of the composites were tested, their microstructures and fracture morphologies were observed using optical microscope (OM), scanning electron microscopy (SEM) and X-ray diffraction (XRD). It was found that the addition of CaSiO3 particles influenced the microstructure and mechanical properties of specimens significantly. The CaSiO3 precipitates from the overlap of adjacent tracks and became the origin of the defects. The tensile strength of specimens range 320-722MPa. The microhardness and elastic modulus are around 250HV and 215GPa respectively. These composites were ductile materials and the fracture mode of the composites was mixed mode of ductile and brittle fracture. The 316L SS/CaSiO3 composites can be a potential biomedical metallic materials in the medical field. Copyright © 2016. Published by Elsevier B.V.

  13. Characterization of un-hydrated and hydrated BioAggregate™ and MTA Angelus™.

    Science.gov (United States)

    Camilleri, J; Sorrentino, F; Damidot, D

    2015-04-01

    BioAggregate™ is a novel material introduced for use as a root-end filling material. It is tricalcium silicate-based, free of aluminium and uses tantalum oxide as radiopacifier. BioAggregate contains additives to enhance the material performance. The purpose of this research was to characterize the un-hydrated and hydrated forms of BioAggregate using a combination of techniques, verify whether the additives if present affect the properties of the set material and compare these properties to those of MTA Angelus™. Un-hydrated and hydrated BioAggregate and MTA Angelus were assessed. Un-hydrated cement was tested for chemical composition, specific surface area, mineralogy and kinetics of hydration. The set material was investigated for mineralogy, microstructure and bioactivity. Scanning electron microscopy, X-ray energy dispersive spectroscopic analysis, X-ray fluorescence spectroscopy, X-ray diffraction and isothermal calorimetry were employed. The specific surface area was investigated using a gas adsorption method with nitrogen as the probe. BioAggregate was composed of tricalcium silicate, tantalum oxide, calcium phosphate and silicon dioxide and was free of aluminium. On hydration, the tricalcium silicate produced calcium silicate hydrate and calcium hydroxide. The former was deposited around the cement grains, while the latter reacted with the silicon dioxide to form additional calcium silicate hydrate. This resulted in reduction of calcium hydroxide in the aged cement. MTA Angelus reacted in a similar fashion; however, since it contained no additives, the calcium hydroxide was still present in the aged cement. Bioactivity was demonstrated by deposition of hydroxyapatite. BioAggregate exhibited a high specific surface area. Nevertheless, the reactivity determined by isothermal calorimetry appeared to be slow compared to MTA Angelus. The tantalum oxide as opposed to bismuth oxide was inert, and tantalum was not leached in solution. BioAggregate exhibited

  14. Cytotoxicity and Osteogenic Potential of Silicate Calcium Cements as Potential Protective Materials for Pulpal Revascularization

    Science.gov (United States)

    Bortoluzzi, Eduardo A.; Niu, Li-na; Palani, Chithra D.; El-Awady, Ahmed R.; Hammond, Barry D.; Pei, Dan-dan; Tian, Fu-cong; Cutler, Christopher W.; Pashley, David H.; Tay, Franklin R.

    2016-01-01

    Objectives In pulpal revascularization, a protective material is placed coronal to the blood clot to prevent recontamination and to facilitate osteogenic differentiation of mesenchynal stem cells to produce new dental tissues. Although mineral trioxide aggregate (MTA) has been the material of choice for clot protection, it is easily displaced into the clot during condensation. The present study evaluated the effects of recently-introduced calcium silicate cements (Biodentine and TheraCal LC) on the viability and osteogenic differentiation of human dental pulp stem cells (hDPSCs) by comparing with MTA Angelus. Methods Cell viability was assessed using XTT assay and flow cytometry. The osteogenic potential of hDPSCs exposed to calcium silicate cements was examined using qRT-PCR for osteogeic gene expressions, alkaline phosphatase enzyme activity, Alizarin red S staining and transmission electron microscopy of extracellular calcium deposits. Parametric statistical methods were employed for analyses of significant difference among groups, with α=0.05. Results The cytotoxic effects of Biodentine and TheraCal LC on hDPSCs were time- and concentration-dependent. Osteogenic differentiation of hDPSCs was enhanced after exposure to Biodentine that was depleted of its cytotoxic components. This effect was less readily observed in hDPSCs exposed to TheraCal LC, although both cements supported extracelluar mineralization better than the positive control (zinc oxide-eugenol–based cement). Significance A favorable tissue response is anticipated to occur with the use of Biodentine as a blood clot-protecting material for pulpal revascularizaiton. Further investigations with the use of in vivo animal models are required to validate the potential adverse biological effects of TheraCal LC on hDPSCs. PMID:26494267

  15. Cytotoxicity and osteogenic potential of silicate calcium cements as potential protective materials for pulpal revascularization.

    Science.gov (United States)

    Bortoluzzi, Eduardo A; Niu, Li-Na; Palani, Chithra D; El-Awady, Ahmed R; Hammond, Barry D; Pei, Dan-Dan; Tian, Fu-Cong; Cutler, Christopher W; Pashley, David H; Tay, Franklin R

    2015-12-01

    In pulpal revascularization, a protective material is placed coronal to the blood clot to prevent recontamination and to facilitate osteogenic differentiation of mesenchymal stem cells to produce new dental tissues. Although mineral trioxide aggregate (MTA) has been the material of choice for clot protection, it is easily displaced into the clot during condensation. The present study evaluated the effects of recently introduced calcium silicate cements (Biodentine and TheraCal LC) on the viability and osteogenic differentiation of human dental pulp stem cells (hDPSCs) by comparing with MTA Angelus. Cell viability was assessed using XTT assay and flow cytometry. The osteogenic potential of hDPSCs exposed to calcium silicate cements was examined using qRT-PCR for osteogenic gene expressions, alkaline phosphatase enzyme activity, Alizarin red S staining and transmission electron microscopy of extracellular calcium deposits. Parametric statistical methods were employed for analyses of significant difference among groups, with α=0.05. The cytotoxic effects of Biodentine and TheraCal LC on hDPSCs were time- and concentration-dependent. Osteogenic differentiation of hDPSCs was enhanced after exposure to Biodentine that was depleted of its cytotoxic components. This effect was less readily observed in hDPSCs exposed to TheraCal LC, although both cements supported extracellular mineralization better than the positive control (zinc oxide-eugenol-based cement). A favorable tissue response is anticipated to occur with the use of Biodentine as a blood clot-protecting material for pulpal revascularization. Further investigations with the use of in vivo animal models are required to validate the potential adverse biological effects of TheraCal LC on hDPSCs. Copyright © 2015 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

  16. Crystal structure of magnesium silicate hydrates (M-S-H): The relation with 2:1 Mg–Si phyllosilicates

    Energy Technology Data Exchange (ETDEWEB)

    Roosz, Cédric, E-mail: c.roosz@brgm.fr [Andra — Scientific Division, 1-7 Rue Jean Monnet, Parc de la Croix Blanche, 92298 Chatenay-Malabry Cedex (France); BRGM, 3 Avenue Claude Guillemin, 45060 Orléans Cedex 2 (France); Grangeon, Sylvain; Blanc, Philippe [BRGM, 3 Avenue Claude Guillemin, 45060 Orléans Cedex 2 (France); Montouillout, Valérie [CNRS, CEMHTI, UPR 3079, 45071 Orléans (France); Lothenbach, Barbara [Empa, Laboratory for Concrete & Construction Chemistry, Überlandstrasse 129, 8600 Dübendorf (Switzerland); Henocq, Pierre; Giffaut, Eric [Andra — Scientific Division, 1-7 Rue Jean Monnet, Parc de la Croix Blanche, 92298 Chatenay-Malabry Cedex (France); Vieillard, Philippe [Université de Poitiers-CNRS, UMR7285 IC2MP, Equipe HydrASA, Poitiers 86022 (France); Gaboreau, Stéphane [BRGM, 3 Avenue Claude Guillemin, 45060 Orléans Cedex 2 (France)

    2015-07-15

    Two magnesium silicate hydrates (M-S-H) with structural magnesium/silicon ratios of 0.57 ± 0.08 and 1.07 ± 0.13 were synthesized at room temperature, with one year of synthesis duration. Their structure was clarified by considering results from X-ray diffraction, TEM, {sup 29}Si MAS NMR spectroscopy, TGA, and EPMA. A modeling approach appropriate to defective minerals was used because usual XRD refinement techniques cannot be used in the case of turbostratic samples, where coherency between successive layers is lost. M-S-H with Mg/Si ratio of ~ 0.6 appears to be structurally close to nanocrystalline turbostratic 2:1 Mg–Si phyllosilicates. The increase of the Mg/Si ratio from 0.6 to 1.2 occurs by increasing the occurrence of defects in the silicate plan. The layer-to-layer distance evolves from 9.46 Å to 14 Å under air-dried and ethylene glycol conditions, respectively. Crystallites have a mean size of 1.5 nm in the ab plane, and 2.4 nm along c*.

  17. The effect of root dentin conditioning protocols on the push-out bond strength of three calcium silicate sealers

    NARCIS (Netherlands)

    Neelakantan, P.; Nandagopal, M.; Shemesh, H.; Wesselink, P.R.

    2015-01-01

    Objectives: To compare the effects of irrigation protocols on the push-out bond strength of calcium silicate materials at two different time periods (7-days and 3-months). Materials and methods: Root canals (n=300) were irrigated with one of the following (n=60): group 1 (3% NaOCl-17% EDTA); group 2

  18. Success Rates of Pulpotomies in Primary Molars Using Calcium Silicate-Based Materials: A Randomized Control Trial

    National Research Council Canada - National Science Library

    Yeliz Guven; Sermin Dicle Aksakal; Nilufer Avcu; Gulcan Unsal; Elif Bahar Tuna; Oya Aktoren

    2017-01-01

    Objective. The aim of this study was to evaluate and compare, both clinically and radiographically, the effects of calcium silicate-based materials (i.e., ProRoot MTA [PR-MTA], MTA-Plus [MTA-P], and Biodentine [BD...

  19. Impact of Micro Silica Surface Hydroxyl Groups on the Properties of Calcium Silicate Products

    DEFF Research Database (Denmark)

    Haastrup, Sonja; Jørgensen, Bianca; Yu, Donghong

    2017-01-01

    of calcium silicate. We increase the hydroxyl groups by dispersing the micro silica in 10wt% H2O2 (CS10%), and we remove the hydroxyl groups by drying the micro silica at 650°C and then disperse it in water (CS650). A reference sample is also prepared from as-received micro silica dispersed in water (CSref...... for sample CS10% and the crystal phase tobermorite increase compared to CSref. Sample CS650 is mainly composed of Ca(OH)2 after reaction, and hardly any xonotlite and tobermorite crystal phase found. The compressive strength is found to increase for CS10%. The linear shrinkage also increases, which is caused...

  20. 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.

  1. 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.

  2. [Endodontics in motion: new concepts, materials and techniques 1. Hydraulic Calcium Silicate Cements].

    Science.gov (United States)

    Moinzadeh, A T; Jongsma, L; de Groot-Kuin, D; Cristescu, R; Neirynck, N; Camilleri, J

    2015-01-01

    Hydraulic Calcium Silicate Cements (HCSCs) constitute a group of materials that have become increasingly popular in endodontics since the introduction of Mineral Trioxide Aggregate (MTA) in the 1990s. MTA is Portland cement to which bismuth oxide has been added to increase its radiopacity. The most important property of MTA is its capacity to set in water or a humid environment. However, MTA also has important limitations, for example, it's difficult to work with and can discolour teeth. Recently, numerous products based on HCSC chemistry, which can be considered as modifications of MTA intended to reduce its limitations, have become available on the market. Despite their potential advantages, all of these materials have their own specific limitations that are currently insufficiently known and investigated.

  3. Calcium polyphosphate as an additive to zinc-silicate glass ionomer cements.

    Science.gov (United States)

    Valliant, Esther Mae; Gagnier, David; Dickey, Brett Thomas; Boyd, Daniel; Filiaggi, Mark Joseph

    2015-07-01

    Aluminum-free glass ionomer cements (GICs) are under development for orthopedic applications, but are limited by their insufficient handling properties. Here, the addition of calcium polyphosphate (CPP) was investigated as an additive to an experimental zinc-silicate glass ionomer cement. A 50% maximum increase in working time was observed with CPP addition, though this was not clinically significant due to the short working times of the starting zinc-silicate GIC. Surprisingly, CPP also improved the mechanical properties, especially the tensile strength which increased by ∼33% after 30 days in TRIS buffer solution upon CPP addition up to 37.5 wt%. This strengthening may have been due to the formation of ionic crosslinks between the polyphosphate chains and polyacrylic acid. Thus, CPP is a potential additive to future GIC compositions as it has been shown to improve handling and mechanical properties. In addition, CPP may stimulate new bone growth and provide the ability for drug delivery, which are desirable modifications for an orthopedic cement. © The Author(s) 2015 Reprints and permissions: sagepub.co.uk/journalsPermissions.nav.

  4. Osteogenic and Angiogenic Response to Calcium Silicate-based Endodontic Sealers.

    Science.gov (United States)

    Costa, Fábio; Sousa Gomes, Pedro; Fernandes, Maria Helena

    2016-01-01

    Calcium silicate-based endodontic sealers are reported to favor the regeneration of periradicular tissues, a process requiring concerted osteogenic and angiogenic events. This study compared 4 calcium silicate-based sealers for the effects of their extracts on osteogenic and angiogenic cell behavior. Extracts from ProRoot MTA (Dentsply Tulsa Dental, Tulsa, OK), MTA Plus (Prevest Denpro Limited, Jammu City, India), MTA Fillapex (Angelus, Londrina, PR, Brazil), and Biodentine (Septodont, Saint-Maur-des-Fosses, France) were prepared from freshly mixed sealers (0.1 g/cm(2)/mL extraction medium) and diluted (1:2-1:20). The sealers were compared for the dose- and time-dependent effects on the proliferation and differentiation of human mesenchymal stem cells (hMSCs) and human umbilical vein endothelial cells (HUVECs). An ex vivo osteogenic assay (regeneration of neonatal mice parietal bone defects) and an in vivo angiogenesis assay (chorioallantoic membrane assay) were performed. Diluted extracts from MTA ProRoot and MTA Plus had evident stimulatory effects on the proliferation of hMSCs, alkaline phosphatase activity, and ex vivo regeneration of bone defects. They also increased HUVEC growth; allowed normal tubularlike network organization; and, in vivo, did not affect angiogenesis. Comparatively, Biodentine also elicited a favorable response on hMSCs and HUVECs, but the overall osteogenic and angiogenic outcome was slightly lower. MTA Fillapex exhibited the highest toxicity in hMSCs and HUVECs and, unlike the other sealers, only allowed a partial regeneration of bone defects. The sealers caused dose- and time-dependent effects on the osteoblastic and endothelial response, eliciting similar cytocompatibility profiles. Results suggest that the induction of both osteogenic and angiogenic events may contribute to the sealers' regenerative outcome. Copyright © 2016 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  5. 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.

  6. Aluminum-induced dreierketten chain cross-links increase the mechanical properties of nanocrystalline calcium aluminosilicate hydrate

    Science.gov (United States)

    Geng, Guoqing; Myers, Rupert J.; Li, Jiaqi; Maboudian, Roya; Carraro, Carlo; Shapiro, David A.; Monteiro, Paulo J. M.

    2017-03-01

    The incorporation of Al and increased curing temperature promotes the crystallization and cross-linking of calcium (alumino)silicate hydrate (C-(A-)S-H), which is the primary binding phase in most contemporary concrete materials. However, the influence of Al-induced structural changes on the mechanical properties at atomistic scale is not well understood. Herein, synchrotron radiation-based high-pressure X-ray diffraction is used to quantify the influence of dreierketten chain cross-linking on the anisotropic mechanical behavior of C-(A-)S-H. We show that the ab-planar stiffness is independent of dreierketten chain defects, e.g. vacancies in bridging tetrahedra sites and Al for Si substitution. The c-axis of non-cross-linked C-(A-)S-H is more deformable due to the softer interlayer opening but stiffens with decreased spacing and/or increased zeolitic water and Ca2+ of the interlayer. Dreierketten chain cross-links act as ‘columns’ to resist compression, thus increasing the bulk modulus of C-(A-)S-H. We provide the first experimental evidence on the influence of the Al-induced atomistic configurational change on the mechanical properties of C-(A-)S-H. Our work advances the fundamental knowledge of C-(A-)S-H on the lowest level of its hierarchical structure, and thus can impact the way that innovative C-(A-)S-H-based cementitious materials are developed using a ‘bottom-up’ approach.

  7. Bioactivity and biomineralization ability of calcium silicate-based pulp-capping materials after subcutaneous implantation.

    Science.gov (United States)

    Hinata, G; Yoshiba, K; Han, L; Edanami, N; Yoshiba, N; Okiji, T

    2017-06-26

    To evaluate the abilities of three calcium silicate-based pulp-capping materials (ProRoot MTA, TheraCal LC and a prototype tricalcium silicate cement) to produce apatite-like precipitates after being subcutaneously implanted into rats. Polytetrafluoroethylene tubes containing each material were subcutaneously implanted into the backs of Wistar rats. At 7, 14 and 28 days post-implantation, the implants were removed together with the surrounding connective tissue, and fixed in 2.5% glutaraldehyde in cacodylate buffer. The chemical compositions of the surface precipitates formed on the implants were analysed with scanning electron microscopy-electron probe microanalysis (SEM-EPMA). The distributions of calcium (Ca) and phosphorus (P) at the material-tissue interface were also analysed with SEM-EPMA. Comparisons of the thicknesses of the Ca- and P-rich areas were performed using the Friedman test followed by Scheffe's test at a significant level of 5%. All three materials produced apatite-like surface precipitates containing Ca and P. For each material, elemental mapping detected a region of connective tissue in which the concentrations of Ca and P were higher than those in the surrounding connective tissue. The thickness of this Ca- and P-rich region exhibited the following pattern: ProRoot MTA > prototype tricalcium silicate cement ≥ TheraCal LC. ProRoot MTA had a significantly thicker layer of Ca and P than the other materials at all time-points (P < 0.05), and a significant difference was detected between the prototype cement and TheraCal LC at 28 days (P < 0.05). After being subcutaneously implanted, all of the materials produced Ca- and P-containing surface precipitates and a Ca- and P-rich layer within the surrounding tissue. The thickness of the Ca- and P-rich layer of ProRoot MTA was significantly thicker than that of the other materials. © 2017 International Endodontic Journal. Published by John Wiley & Sons Ltd.

  8. Hydrothermal Synthesis of Dicalcium Silicate Based Cement

    Science.gov (United States)

    Dutta, N.; Chatterjee, A.

    2017-06-01

    It is imperative to develop low energy alternative binders considering the large amounts of energy consumed as well as carbon dioxide emissions involved in the manufacturing of ordinary Portland cement. This study is on the synthesis of a dicalcium silicate based binder using a low temperature hydrothermal route.The process consists of synthesizing an intermediate product consisting of a calcium silicate hydrate phase with a Ca:Si ratio of 2:1 and further thermal treatment to produce the β-Ca2SiO4 (C2S) phase.Effect of various synthesis parameters like water to solid ratio, dwell time and temperature on the formation of the desired calcium silicate hydrate phase is reported along with effect of heating conditions for formation of the β-C2S phase. Around 77.45% of β-C2S phase was synthesized by thermal treatment of the intermediate phase at 820°C.

  9. 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. Copyright © 2016 Elsevier B.V. All rights reserved.

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

    Directory of Open Access Journals (Sweden)

    Selen Küçükkaya

    2016-01-01

    Full Text Available 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<0.05. 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<0.05. Despite the significant changes in cell viability over time, materials presented similar cytotoxicity profile. Biodentine and CEM can be considered as alternative materials for root-end surgery procedures.

  11. Lime and calcium-magnesium silicate in the ionic speciation of an Oxisol

    Directory of Open Access Journals (Sweden)

    João Arthur Antonangelo

    Full Text Available ABSTRACT Plant residues and certain fertilizers accelerate soil acidification and increase the levels of aluminum-Al+3 in soils under no-tillage (NT. Silicates act as acidity amendments and as a source of silicon as in H4SiO4. An increase in the pH of soil solution causes the deprotonation of H4SiO4 and generates the anionic form (H3SiO4−. The aim of this study was to evaluate the ionic speciation of Si, Al, Ca, Mg and K in aqueous extracts by means of a software calculation. Since 2006, a field experiment has been under way on an Oxisol under NT subjected to lime and calcium-magnesium silicate applications under four crop systems. The amendments were applied in Oct 2006 and in Oct 2011, aiming to raise base saturation to 70 %. Soil samples were collected in Oct 2013, at depths of 0-5, 5-10, 10-20, 20-40 and 40-60 cm. Both Ca and Mg formed complexes with dissolved organic carbon (DOC whereas the same was not observed for potassium. These three basic cations were mostly in their free forms regardless of treatment, while Al was mostly complexed with DOC even at the lowest depths (40-60 cm. The highest value of free Al form was 15 %. Si was almost 100 % as H4SiO4, and its activity was similar to its concentration in solution for all crop systems and at all depths, regardless of amendment applied. The percentages of H3SiO4− and Al-H3SiO42+ were irrelevant, providing more phytoavailable H4SiO4 in soil solution.

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

    Science.gov (United States)

    Onani, Martin O.; Dejene, Francis B.

    2014-04-01

    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.

  13. Calcium Silicate Improved Bioactivity and Mechanical Properties of Poly(3-hydroxybutyrate-co-3-hydroxyvalerate Scaffolds

    Directory of Open Access Journals (Sweden)

    Cijun Shuai

    2017-05-01

    Full Text Available The poor bioactivity and mechanical properties have restricted its biomedical application, although poly(3-hydroxybutyrate-co-3-hydroxyvalerate (PHBV had good biocompatibility and biodegradability. In this study, calcium silicate (CS was incorporated into PHBV for improving its bioactivity and mechanical properties, and the porous PHBV/CS composite scaffolds were fabricated via selective laser sintering (SLS. Simulated body fluid (SBF immersion tests indicated the composite scaffolds had good apatite-forming ability, which could be mainly attributed to the electrostatic attraction of negatively charged silanol groups derived from CS degradation to positively charged calcium ions in SBF. Moreover, the compressive properties of the composite scaffolds increased at first, and then decreased with increasing the CS content, which was ascribed to the fact that CS of a proper content could homogeneously disperse in PHBV matrix, while excessive CS would form continuous phase. The compressive strength and modulus of composite scaffolds with optimal CS content of 10 wt % were 3.55 MPa and 36.54 MPa, respectively, which were increased by 41.43% and 28.61%, respectively, as compared with PHBV scaffolds. Additionally, 3-(4,5-dimethylthiazol-2-yl-2,5-diphenyltetrazolium bromide (MTT assay indicated MG63 cells had a higher proliferation rate on PHBV/CS composite scaffolds than that on PHBV. Alkaline phosphatase (ALP staining assay demonstrated the incorporation of CS significantly promoted osteogenic differentiation of MG63 cells on the scaffolds. These results suggest that the PHBV/CS composite scaffolds have the potential in serving as a substitute in bone tissue engineering.

  14. Effect of Different Irrigation Solutions on the Colour Stability of Three Calcium Silicate-Based Materials.

    Science.gov (United States)

    F, Sobhnamayan; A, Adl; S, Ghanbaran

    2017-06-01

    Previous studies have shown discoloration of mineral trioxide aggregate (MTA) in contact with root canal irrigation solutions. However, there are limited data on colour stability of other calcium silicate-based materials (CSMs). This in vitro study aimed to evaluate the colour stability of three CSMs in contact with different irrigation solutions. Three CSMs including White MTA (wMTA) Angelus, calcium enriched mixture (CEM), and Biodentine were assessed in this study. Forty five samples of each material were mixed according to the manufactures' instructions and then placed in silicone tubes. After 24 hours, the materials were removed from the moulds and 9 samples of each material left dry or immersed in normal saline, 5% sodium hypochlorite (NaOCL), 2% chlorhexidinegluconate (CHX), or 17%EDTA for 24 hours. Colour changes were measured with a spectrophotometer. Data were evaluated with 2-way analysis of variance, one way analysis of variance and Tukey post hoc tests. The highest discoloration of all materials was observed after contact with CHX. In the MTA Angelus and CEM cement groups, significant differences were observed between CHX and NaOCl and also between these two irrigants with the other three irrigants ( p < 0.05). In the Biodentine group, CHX created statistically significant discoloration compared to other irrigants ( p < 0.05). Only wMTA Angelus showed a significantly higher discoloration in contact with EDTA compared to normal saline and dry condition ( p < 0.05). wMTA Angelus showed a significantly higher colour change compared with CEM cement and Biodentine after contact with NaOCl, CHX, and EDTA ( p < 0.05). The contact of wMTA, CEM cement, and Biodentine with CHX should be avoided because this leads to severe discoloration. Contact with sodium hypochlorite also leads to discoloration of wMTA and CEM cements. Among of the three tested materials, wMTA showed the highest discoloration after contact with NaOCl, CHX, and EDTA.

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

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Ming-Hsien [Institute of Oral Science, Chung Shan Medical University, Taichung City, Taiwan (China); Shen, Yu-Fang; Hsu, Tuan-Ti [3D Printing Medical Research Center, China Medical University Hospital, China Medical University, Taichung City, Taiwan (China); Huang, Tsui-Hsien [School of Dentistry, Chung Shan Medical University, Taichung City, Taiwan (China); Department of Stomatology, Chung Shan Medical University Hospital, Taichung City, Taiwan (China); Shie, Ming-You, E-mail: eviltacasi@gmail.com [3D Printing Medical Research Center, China Medical University Hospital, China Medical University, Taichung City, Taiwan (China)

    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 0–10 mM 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. - Highlights: • The hinokitiol-modified CS up-regulation of odontogenic of hDPCs. • Promoted proliferation of hDPCs on hinokitiol-modified CS. • The hinokitiol-modified CS cements not only inhibited the expression level of inflammatory cytokines, but also had better cytocompatibility. • The hinokitiol-modified CS up-regulation of odontogenic of hPDLs.

  16. Osteoblast-like cell responses to ion products released from magnesium- and silicate-containing calcium carbonates.

    Science.gov (United States)

    Yamada, Shinya; Ota, Yoshio; Obata, Akiko; Kasuga, Toshihiro

    2017-01-01

    Inorganic ions released from bioceramics and bioactive glasses have been reported to influence osteogenic cell functions. Cell responses depend on types of the ions provided, for example, silicate ion has been found to up-regulate their proliferation, differentiation and mineralization. Mouse osteoblast-like cells (MC3T3-E1) were cultured in media containing silicate and calcium ions with/without magnesium ion to evaluate their combined effects on the cell's functions. The cells were cultured in the media containing the extract of silicate-containing vaterite (SiV) and magnesium- and siloxane-containing one (MgSiV) and normal medium and then their adhesion, proliferation, differentiation and mineralization were evaluated. The adhesion of the cells was enhanced when they were cultured in the medium containing MgSiV-extract. Their proliferation and differentiation were up-regulated in both media containing MgSiV-extract and SiV-extract. In particular, the MgSiV-extract significantly enhanced their differentiation than the SiV-extract. This was supported by the mineralization test's results, which showed a large amount of mineral deposit was observed in the cells cultured in the MgSiV-extract medium. Providing the three kinds of ions was effective for up-regulating the cell's mineralization compared to providing silicate and calcium ions without magnesium ion.

  17. Effect of calcium and magnesium silicate on the growth of the castor oil plant subjected to salinity levels

    OpenAIRE

    de Brito Neto, Jose Felix [UNESP; Macedo Beltrao, Napoleao de Esberard; Gonsiorkiewicz Rigon, Joao Paulo [UNESP; Capuani, Silvia [UNESP

    2012-01-01

    Salt stress decreases the osmotic potential of soil solution causing water stress, causing toxic effects in the plants resulting in injuries on the metabolism and nutritional disorders, thus compromising the plant growth, resulting in lower production. The calcium silicate and magnesium can perform the same function as limestone, besides providing silicon to plants, may also contribute to the resistance of plants to salt stress. Thus, the objective of this study was to evaluate the effect of ...

  18. Biocompatibility of three new calcium silicate-based endodontic sealers on human periodontal ligament stem cells.

    Science.gov (United States)

    Collado-González, M; García-Bernal, D; Oñate-Sánchez, R E; Ortolani-Seltenerich, P S; Lozano, A; Forner, L; Llena, C; Rodríguez-Lozano, F J

    2017-09-01

    To evaluate the biocompatibility of three calcium silicate-based endodontic sealers, Bioroot BC Sealer (Septodont, Saint-Maur-des-Fosses, France), Endoseal MTA (EndoSeal, Maruchi, Seoul, Korea) and Nano-ceramic Sealer (B&L Biotech, Fairfax, VA, USA) (NCS), on human periodontal ligament stem cells (hPDLSCs). Human periodontal ligament stem cells were cultured in the presence of various endodontic sealer eluates for 24 h. Cell viability was determined using the MTT assay. Cell death and changes in phenotype induced by the set endodontic sealer eluates were evaluated through flow cytometry. Also, an in vitro scratch wound-healing model was used to determine their effects in cell migration. Finally, to assess cell morphology and attachment to the different sealers, hPDLSCs were directly seeded onto the material surfaces and analysed by scanning electron microscopy (SEM). One-way analysis of variance (anova) followed by a Bonferroni post-test was performed (P endodontic sealers for clinical application. © 2016 International Endodontic Journal. Published by John Wiley & Sons Ltd.

  19. Carboxymethyl fenugreek galactomannan-gellan gum-calcium silicate composite beads for glimepiride delivery.

    Science.gov (United States)

    Bera, Hriday; Mothe, Srilatha; Maiti, Sabyasachi; Vanga, Sridhar

    2017-09-13

    Novel carboxymethyl fenugreek galactomannan (CFG)-gellan gum (GG)-calcium silicate (CS) composite beads were developed for controlled glimepiride (GLI) delivery. CFG having degree of carboxymethylation of 0.71 was synthesized and characterized by FTIR, DSC and XRD analyses. Subsequently, GLI-loaded hybrids were accomplished by ionotropic gelation technique employing Ca+2/Zn+2/Al+3 ions as cross-linkers. All the formulations demonstrated excellent drug encapsulation efficiency (DEE, 48-97%) and sustained drug release behaviour (Q8h, 62-94%). These quality attributes were remarkably influenced by polymer-blend (GG:CFG) ratios, cross-linker types and CS inclusion. The drug release profile of the optimized formulation (F-6) was best fitted in zero-order model with anomalous diffusion driven mechanism. It also conferred excellent ex vivo mucoadhesive property and considerable hypoglycemic effect in streptozotocin-induced diabetic rats. Furthermore, the beads were characterized for drug-excipients compatibility, drug crystallinity, thermal behaviour and surface morphology. Thus, the developed hybrid matrices are appropriate for controlled delivery of GLI for Type 2 diabetes management. Copyright © 2017 Elsevier B.V. All rights reserved.

  20. Graphene Nanosheets to Improve Physico-Mechanical Properties of Bioactive Calcium Silicate Cements

    Directory of Open Access Journals (Sweden)

    Nileshkumar Dubey

    2017-05-01

    Full Text Available Bioactive calcium silicate cements are widely used to induce mineralization, to cement prosthetic parts, in the management of tooth perforations, and other areas. Nonetheless, they can present clinical disadvantages, such as long setting time and modest physico-mechanical properties. The objective of this work was to evaluate the potential of graphene nanosheets (GNS to improve two bioactive cements. GNS were obtained via reduction of graphite oxide. GNS were mixed (1, 3, 5, and 7 wt % with Biodentine (BIO and Endocem Zr (ECZ, and the effects on setting time, hardness, push-out strength, pH profile, cell proliferation, and mineralization were evaluated. Statistics were performed with two-way ANOVA and Tukey test (α = 0.05. GNS has not interfered in the composition of the set cements as confirmed by Raman, FT-IR and XRD. GNS (1 and 3 wt % shortened the setting time, increased hardness of both materials but decreased significantly the push-out strength of ECZ. pH was not affected but 1 wt % and 7 wt % to ECZ and 5 wt % to BIO increased the mineralization compared to the controls. In summary, GNS may be an alternative to improve the physico-mechanical properties and bioactivity of cements. Nonetheless, the use of GNS may not be advised for all materials when effective bonding is a concern.

  1. 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.

  2. 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.

  3. 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.

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

    Directory of Open Access Journals (Sweden)

    S. Koubi

    2012-01-01

    Full Text Available 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 (=10 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, Cuxhaven, Germany in open-sandwich restorations covered with a light-cured composite. Positive (=5 and negative (=5 controls were included. The teeth simultaneously underwent thermocycling and mechanocycling using a fatigue cycling machine (1,440 cycles, 5–55°C; 86,400 cycles, 50 N/cm2. The specimens were then stored in phosphate-buffered saline to simulate aging. After 1 year, the teeth were submitted to glucose diffusion, and the resulting data were analyzed with a nonparametric Mann-Whitney test. The Biodentine group and the Ionolux group presented glucose concentrations of 0.074 ± 0.035 g/L and 0.080 ± 0.032 g/L, respectively. No statistically significant differences were detected between the two groups. Therefore, the calcium silicate-based material performs as well as the resin-modified glass ionomer cement in open-sandwich restorations.

  5. Application of soil block without burning process and calcium silicate panels as building wall in mountainous area

    Science.gov (United States)

    Noerwasito, Vincentius Totok; Nasution, Tanti Satriana Rosary

    2017-11-01

    Utilization of local building materials in a residential location in mountainous area is very important, considering local material as a low-energy building material because of low transport energy. The local building materials used in this study are walls made from soil blocks. The material was made by the surrounding community from compacted soil without burning process. To maximize the potential of soil block to the outdoor temperature in the mountains, it is necessary to add non-local building materials as an insulator from the influence of the outside air. The insulator was calcium silicate panel. The location of the research is Trawas sub-district, Mojokerto regency, which is a mountainous area. The research problem is on applying the composition of local materials and calcium silicate panels that it will be able to meet the requirements as a wall building material and finding to what extent the impact of the wall against indoor temperature. The result from this research was the application of soil block walls insulated by calcium silicate panels in a building model. Besides, because of the utilization of those materials, the building has a specific difference between indoor and outdoor temperature. Thus, this model can be applied in mountainous areas in Indonesia.

  6. Sol-gel synthesis and characterizations of hybrid chitosan-PEG/calcium silicate nanocomposite modified with ZnO-NPs and (E102) for optical and antibacterial applications.

    Science.gov (United States)

    Youssef, Ahmed M; El-Nahrawy, Amany M; Abou Hammad, Ali B

    2017-04-01

    Hybrid Chitosan/Poly ethylene glycol/calcium silicate (CS/PEG/calcium silicate) nanocomposite modified with different two types, zinc oxide nanoparticles (ZnO-NPs) and tartrazine dye (E102) were prepared by sol gel method and the characterization of their structure and biological properties were carried out in order to evaluate the possible use in optical and biomedical fields. The hybrid CS/PEG/calcium silicate complex formations have been established by X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopic analysis. The spheres-like chitosan-PEG/calcium silicate and modified with both ZnO-NPs and (E102) were obtained with optimum concentration of 11% ZnO-NPs and 0.3gm (E102) dyes. Spheres-like particle shape of these nanocomposites from SEM images, higher UV absorption in the region of 200-300nm by UV-vis absorption spectrophotometer are recorded. The fabricate CS/PEG/calcium silicate nanocomposites and doped with ZnO-NPs and tetrazine were studied contrary to gram positive (Staphylococcus aureus), gram negative (Pseudomonas aeruginosa) bacteria, fungi (Candidia albicans) and Aspargillus niger via the agar plate method. The obtained results indicated that the prepared CS-PEG/calcium silicate nanocomposites have good antibacterial properties agnist G(+ve), G(-ve) bacteria and fungi, so that it could be a promised candidate in various optical and in biological applications as well as packaging application. Copyright © 2017 Elsevier B.V. All rights reserved.

  7. Solidification/stabilization and leaching behavior of PbCl₂ in fly-ash hydrated silicate matrix and fly-ash geopolymer matrix.

    Science.gov (United States)

    Li, Yang; Gao, Xingbao; Wang, Qi; He, Jie; Yan, Dahai

    2015-05-01

    Fly ash (FA) for reuse as a construction material is activated using two methods, to produce hydrated silicate and geopolymer gels. We investigated the solidification/stabilization and leaching behavior of PbCl2 in a geopolymer matrix (GM) and hydrated silicate matrix (HSM), based on FA as the source material, to evaluate the environmental and health risks. The GM and HSM synthetic conditions were 60 °C, 20 % relative humidity (RH), and 12 wt% (6 mol/L) NaOH, and 20 ± 2 °C, ≥ 90 % RH, and 30 wt.%, respectively, based on their compressive strength performances. X-ray diffraction (XRD) showed that Pb participated in hydration and geopolymerization, and was incorporated in the structural components of the hydrated silicate and geopolymer. In leaching experiments, the solidification/stabilization effects of Pb and Cl in the HSM and GM improved with increasing curing time. After long-term curing (28 days), the immobility of Pb in the GM was better than that in the HSM. Sodalite improved the Cl-stabilizing ability of the GM compared with that of the HSM. In static monolithic leaching experiments, HSM and GM had the same Pb-leaching behaviors. Based on the changes in the location of the neutral sphere layer with decreasing acid-neutralizing capacity, Pb release was divided into alkaline-release, stagnation, and acid-release stages. The neutral sphere layer contained the highest Pb concentration during permeation toward the block center from the block edge. This behavior regulation could also apply to other amphoteric metals immobilized by GMs and HSMs.

  8. A Comparative Chemical Study of Calcium Silicate-Containing and Epoxy Resin-Based Root Canal Sealers

    Directory of Open Access Journals (Sweden)

    Przemysław Reszka

    2016-01-01

    Full Text Available Objective. The present study assessed the chemical elements in two novel calcium silicate-containing root canal sealers, BioRoot RCS and Well-Root ST, compared to a calcium silicate-containing root canal sealer that has been on the market for several years, MTA Fillapex, and epoxy resin-based sealer AHPlus. Material and Methods. The sealers were mixed and manipulated according to the manufacturers’ instructions. Twelve cylindrical molds (inner diameter 4 mm; height 3 mm were placed on a glass petri dish and packed with the materials. The dish was transferred to an incubator. After 72 h the molds were examined by scanning electron microscopy and energy dispersive X-ray microanalysis. Results. BioRoot RCS and Well-Root ST had high peaks of calcium, zirconium, oxygen, carbon, silicon, and chlorine. Well-Root ST also had sodium, magnesium, aluminum, and titanium peaks. MTA Fillapex and AHPlus had carbon, oxygen, calcium, titanium, and bismuth peaks. A silicon peak was also observed for MTA Fillapex, and zirconium and tungsten peaks for AHPlus. Conclusion. BioRoot RSC had the highest degree of purity. The clinical implication of metals contained in the other sealers needs to be investigated.

  9. A Comparative Chemical Study of Calcium Silicate-Containing and Epoxy Resin-Based Root Canal Sealers.

    Science.gov (United States)

    Reszka, Przemysław; Nowicka, Alicja; Lipski, Mariusz; Dura, Włodzimierz; Droździk, Agnieszka; Woźniak, Krzysztof

    2016-01-01

    Objective. The present study assessed the chemical elements in two novel calcium silicate-containing root canal sealers, BioRoot RCS and Well-Root ST, compared to a calcium silicate-containing root canal sealer that has been on the market for several years, MTA Fillapex, and epoxy resin-based sealer AHPlus. Material and Methods. The sealers were mixed and manipulated according to the manufacturers' instructions. Twelve cylindrical molds (inner diameter 4 mm; height 3 mm) were placed on a glass petri dish and packed with the materials. The dish was transferred to an incubator. After 72 h the molds were examined by scanning electron microscopy and energy dispersive X-ray microanalysis. Results. BioRoot RCS and Well-Root ST had high peaks of calcium, zirconium, oxygen, carbon, silicon, and chlorine. Well-Root ST also had sodium, magnesium, aluminum, and titanium peaks. MTA Fillapex and AHPlus had carbon, oxygen, calcium, titanium, and bismuth peaks. A silicon peak was also observed for MTA Fillapex, and zirconium and tungsten peaks for AHPlus. Conclusion. BioRoot RSC had the highest degree of purity. The clinical implication of metals contained in the other sealers needs to be investigated.

  10. Laser Sintered Magnesium-Calcium Silicate/Poly-ε-Caprolactone Scaffold for Bone Tissue Engineering

    Directory of Open Access Journals (Sweden)

    Kuo-Yang Tsai

    2017-01-01

    Full Text Available In this study, we manufacture and analyze bioactive magnesium–calcium silicate/poly-ε-caprolactone (Mg–CS/PCL 3D scaffolds for bone tissue engineering. Mg–CS powder was incorporated into PCL, and we fabricated the 3D scaffolds using laser sintering technology. These scaffolds had high porosity and interconnected-design macropores and structures. As compared to pure PCL scaffolds without an Mg–CS powder, the hydrophilic properties and degradation rate are also improved. For scaffolds with more than 20% Mg–CS content, the specimens become completely covered by a dense bone-like apatite layer after soaking in simulated body fluid for 1 day. In vitro analyses were directed using human mesenchymal stem cells (hMSCs on all scaffolds that were shown to be biocompatible and supported cell adhesion and proliferation. Increased focal adhesion kinase and promoted cell adhesion behavior were observed after an increase in Mg–CS content. In addition, the results indicate that the Mg–CS quantity in the composite is higher than 10%, and the quantity of cells and osteogenesis-related protein of hMSCs is stimulated by the Si ions released from the Mg–CS/PCL scaffolds when compared to PCL scaffolds. Our results proved that 3D Mg–CS/PCL scaffolds with such a specific ionic release and good degradability possessed the ability to promote osteogenetic differentiation of hMSCs, indicating that they might be promising biomaterials with potential for next-generation bone tissue engineering scaffolds.

  11. The effect of obturation technique on the push-out bond strength of calcium silicate sealers.

    Science.gov (United States)

    DeLong, Christopher; He, Jianing; Woodmansey, Karl F

    2015-03-01

    Calcium silicate-based sealers are known to have excellent sealing ability and bioactivities. They are typically recommended to be used in a single-cone (SC) technique. No studies have evaluated the effects of the thermoplastic obturation technique on the dentin interface of these sealers. The purpose of this study was to evaluate the push-out bond strengths of MTA Plus Sealer (Avalon Biomed Inc, Bradenton, FL) and EndoSequence BC Sealer (BC; Brasseler USA, Savannah, GA) when they were used in a thermoplastic technique. Fifty single-rooted human extracted teeth were randomly divided into 5 groups (n = 10), instrumented, and obturated with the SC technique or continuous wave (CW) technique: group 1, BC-SC; group 2, BC-CW; group 3, MTA Plus-SC; group 4, MTA Plus-CW; and group 5, AH Plus (Dentsply DeTrey, Konstanz, Germany)-CW. The roots were sectioned into 1.0-mm-thick slices, and bond strengths were measured using a standardized push-out test. The mode of failure was determined by visual inspection under magnification. The MTA Plus-CW had statistically significant lower bond strengths than all other groups. The BC-SC group had statistically higher bond strengths than the MTA Plus-SC and AH Plus-CW groups. No significant differences were seen among the other groups. Modes of failure were predominately cohesive or mixed except for group 4 (ie, MTA Plus-CW) in which nearly half the specimens had no visible sealer. BC and MTA Plus sealer showed favorable bond strengths when used in an SC technique. The CW obturation technique decreased the bond strengths of these sealers. Copyright © 2015 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  12. Microstructure, Porosity and Mechanical Property Relationships of Calcium-Silicate-Hydrate

    Science.gov (United States)

    1991-02-15

    added NaOH. Although zeolite strengths are not very high, Davidovits (22) has claimed that zeolites and zeolite gels are an important ingredient in his...Mh., pp. 358-364 (1983). 22. Davidovits , J., Geopolymer 󈨜, Vol. 2, Universite de Technologie, Compiegne, France (1988). 23. Wu, X., W. Jiang and

  13. Ultrasonic sound speed of hydrating calcium sulphate hemihydrate; part 2, the correlation of sound velocity to hydration degree

    NARCIS (Netherlands)

    de Korte, A.C.J.; Brouwers, Jos; Fischer, H.B; Matthes, C.; Beuthan, C.

    2011-01-01

    In this article the sound velocity through a mix is correlated to the hydration degree of the mix. Models are presented predicting the sound velocity through fresh slurries and hardened products. These two states correspond to the starting and finishing point of the hydration process. The present

  14. Synthesis, mechanical properties, and in vitro biocompatibility with osteoblasts of calcium silicate-reduced graphene oxide composites.

    Science.gov (United States)

    Mehrali, Mehdi; Moghaddam, Ehsan; Shirazi, Seyed Farid Seyed; Baradaran, Saeid; Mehrali, Mohammad; Latibari, Sara Tahan; Metselaar, Hendrik Simon Cornelis; Kadri, Nahrizul Adib; Zandi, Keivan; Osman, Noor Azuan Abu

    2014-03-26

    Calcium silicate (CaSiO3, CS) ceramics are promising bioactive materials for bone tissue engineering, particularly for bone repair. However, the low toughness of CS limits its application in load-bearing conditions. Recent findings indicating the promising biocompatibility of graphene imply that graphene can be used as an additive to improve the mechanical properties of composites. Here, we report a simple method for the synthesis of calcium silicate/reduced graphene oxide (CS/rGO) composites using a hydrothermal approach followed by hot isostatic pressing (HIP). Adding rGO to pure CS increased the hardness of the material by ∼40%, the elastic modulus by ∼52%, and the fracture toughness by ∼123%. Different toughening mechanisms were observed including crack bridging, crack branching, crack deflection, and rGO pull-out, thus increasing the resistance to crack propagation and leading to a considerable improvement in the fracture toughness of the composites. The formation of bone-like apatite on a range of CS/rGO composites with rGO weight percentages ranging from 0 to 1.5 has been investigated in simulated body fluid (SBF). The presence of a bone-like apatite layer on the composite surface after soaking in SBF was demonstrated by X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). The biocompatibility of the CS/rGO composites was characterized using methyl thiazole tetrazolium (MTT) assays in vitro. The cell adhesion results showed that human osteoblast cells (hFOB) can adhere to and develop on the CS/rGO composites. In addition, the proliferation rate and alkaline phosphatase (ALP) activity of cells on the CS/rGO composites were improved compared with the pure CS ceramics. These results suggest that calcium silicate/reduced graphene oxide composites are promising materials for biomedical applications.

  15. Structural Investigations of Portland Cement Components, Hydration, and Effects of Admixtures by Solid-State NMR Spectroscopy

    DEFF Research Database (Denmark)

    Skibsted, Jørgen Bengaard; Andersen, Morten D.; Jakobsen, Hans Jørgen

    2006-01-01

    - and second-coordination spheres of the spin nucleus under investigation while it is less sensitive to long-range order. Thus, crystalline as well as amorphous phases can be detected in a quantitative manner by solid-state NMR. In particular the structure of the calcium-silicate-hydrate (C-S-H) phase have...... for the C-S-H phase formed during hydration. It will be demonstrated that Al3+ and flouride guest-ions in the anhydrous and hydrated calcium silicates can be studied in detail by 27Al and 19F MAS NMR, thereby providing information on the local structure and the mechanisms for incorporation of these ions...

  16. Tooth Discoloration Induced by Different Calcium Silicate-based Cements: A Systematic Review of In Vitro Studies.

    Science.gov (United States)

    Możyńska, Joanna; Metlerski, Marcin; Lipski, Mariusz; Nowicka, Alicja

    2017-10-01

    On the basis of many clinical observations, some calcium silicate-based cements have a high potential for staining tooth tissue. This feature greatly limits the use of those cements, particularly for anterior teeth. This review aimed to provide a systematic evaluation of published in vitro studies to determine the effect of different calcium silicate-based cements on dental tissue discoloration. This literature review was developed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement. The literature search was based on all publications without a year limit. The last search was performed on October 22, 2016. An electronic search was performed on MEDLINE (PubMed), Cochrane, and Scopus. The articles were selected to address the following research question: Which materials based on calcium silicate-based cements have hard tissue staining potential? The necessary information was extracted by 2 authors independently using a standardized form. The search resulted in 390 titles from all databases. Twenty-three studies met the inclusion criteria. Most of the studies exhibited a moderate risk of bias. The results indicated that some materials showed a strong potential for staining, including gray and white MTA Angelus (Londrina, PR, Brazil), gray and white ProRoot MTA (Dentsply, Tulsa, OK), and Ortho MTA (BioMTA, Seoul, Korea). Individual study results showed that Biodentine (Septodont, Saint Maur des Fosses, France), Retro MTA (BioMTA), Portland cement, EndoSequence Root Repair Material (Brasseler USA, Savannah, GA), Odontocem (Australian Dental Manufacturing, Brisbane, Australia), MM-MTA (Micro Mega, Besancon Cedex, France), and MTA Ledermix (Riemser Pharma GmbH, Greiswald-Insel Riems, Germany) were materials with the smallest staining potential. This review clearly showed that some calcium silicate-based cements have a high potential for staining hard tissue. On the other hand, some showed only a small change in color, which was

  17. How effectively do hydraulic calcium-silicate cements re-mineralize demineralized dentin.

    Science.gov (United States)

    Li, Xin; De Munck, Jan; Van Landuyt, Kirsten; Pedano, Mariano; Chen, Zhi; Van Meerbeek, Bart

    2017-04-01

    To characterize the chemical interplay and to quantify the re-mineralization potential of hydraulic calcium-silicate cements (hCSCs) at demineralized dentin. Pairs of class-I cavities were prepared in non-carious human third molars. One dentin cavity was demineralized with 10% formic acid (5h); the other served as control. The cavities were filled with two resin-free hCSCs (Biodentine, Septodont; ProRoot MTA, Dentsply Sirona) or one resin-based hCSC (TheraCal LC, Bisco). After 1-week, 1-, 3-, and 6-month storage in simulated body fluid (SBF), polished specimen cross-sections were chemically characterized using Field-emission-gun Electron Probe Micro-Analysis (Feg-EPMA) and micro-Raman spectroscopy (μRaman). Feg-EPMA line-scans and elemental mappings confirmed early re-mineralization induced by all three hCSCs at 1week. The relative depth and intensity of re-mineralization were for the resin-free hCSCs in the range of 50.5%-84.8% and 68.1%-89.2%, respectively. Re-mineralization did not significantly differ for the storage periods (p>0.05). Significantly less re-mineralization was achieved by the resin-based hCSC TheraCal LC that reached only at 6months a re-mineralization level that was no longer significantly different from that achieved by the resin-free hCSCs at 1week (p>0.05). Re-mineralization of intertubular dentin, including tubular occlusion, was observed; Si was occasionally detected to have infiltrated the dentin tubules. Dentin re-mineralization by hCSCs was confirmed using μRaman that revealed an increased phosphate peak at 960cm(-1). hCSCs do re-mineralize demineralized dentin. The resin-free cements induced re-mineralization at a higher speed/intensity than the resin-based hCSC. However, re-mineralization was incomplete for all hCSCs tested, this even at 6months. Copyright © 2017 The Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

  18. 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.

  19. 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

  20. 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)

  1. Success Rates of Pulpotomies in Primary Molars Using Calcium Silicate-Based Materials: A Randomized Control Trial

    Directory of Open Access Journals (Sweden)

    Yeliz Guven

    2017-01-01

    Full Text Available Objective. The aim of this study was to evaluate and compare, both clinically and radiographically, the effects of calcium silicate-based materials (i.e., ProRoot MTA [PR-MTA], MTA-Plus [MTA-P], and Biodentine [BD] and ferric sulfate [FS] in pulpotomy of primary molars. Materials and Methods. In this randomized clinical trial, 29 healthy 5- to 7-year-old children with at least four carious primary molars with no clinical or radiographic evidence of pulp degeneration were enrolled. The pulpotomy agents were assigned as follows: Group 1: BD; Group 2: MTA-P; Group 3: PR-MTA; and Group 4: FS. Clinical and radiographic evaluations were performed at 6, 12, and 24 months. Data were analyzed using chi-square tests. Results. Total success rates at 24 months were 82.75%, 86.2%, 93.1%, and 75.86%, respectively. No statistically significant differences in total success rates were observed among the groups at 6-, 12-, and 24-month follow-ups. When the groups were compared according to follow-up times, the success rates in each group did not vary significantly among the 6–12-month, 6–24-month, or 12–24-month periods (p>0.05. Conclusion. Although the success rates of BD, MTA-P, MTA-PR, and FS did not differ significantly, calcium silicate-based materials appeared to be more appropriate than FS in clinical practice.

  2. Success Rates of Pulpotomies in Primary Molars Using Calcium Silicate-Based Materials: A Randomized Control Trial.

    Science.gov (United States)

    Guven, Yeliz; Aksakal, Sermin Dicle; Avcu, Nilufer; Unsal, Gulcan; Tuna, Elif Bahar; Aktoren, Oya

    2017-01-01

    The aim of this study was to evaluate and compare, both clinically and radiographically, the effects of calcium silicate-based materials (i.e., ProRoot MTA [PR-MTA], MTA-Plus [MTA-P], and Biodentine [BD]) and ferric sulfate [FS] in pulpotomy of primary molars. In this randomized clinical trial, 29 healthy 5- to 7-year-old children with at least four carious primary molars with no clinical or radiographic evidence of pulp degeneration were enrolled. The pulpotomy agents were assigned as follows: Group 1: BD; Group 2: MTA-P; Group 3: PR-MTA; and Group 4: FS. Clinical and radiographic evaluations were performed at 6, 12, and 24 months. Data were analyzed using chi-square tests. Total success rates at 24 months were 82.75%, 86.2%, 93.1%, and 75.86%, respectively. No statistically significant differences in total success rates were observed among the groups at 6-, 12-, and 24-month follow-ups. When the groups were compared according to follow-up times, the success rates in each group did not vary significantly among the 6-12-month, 6-24-month, or 12-24-month periods (p > 0.05). Although the success rates of BD, MTA-P, MTA-PR, and FS did not differ significantly, calcium silicate-based materials appeared to be more appropriate than FS in clinical practice.

  3. 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...

  4. Halting of the calcium aluminate cement hydration process; Interrupcao do processo de hidratatacao de um cimento de aluminato de calcio

    Energy Technology Data Exchange (ETDEWEB)

    Luz, A.P.; Borba, N.Z; Pandolfelli, V.C., E-mail: anapaula.light@gmail.com, E-mail: vicpando@power.ufscar.br [Universidade Federal de Sao Carlos (UFSCar), SP (Brazil). Departamento de Engenharia de Materiais

    2011-07-01

    The calcium aluminate cement reactions with water lead to the anhydrous phases dissolution resulting a saturated solution, followed by nucleation and crystal growth of the hydrate compounds. This is a dynamic process, therefore, it is necessary to use suitable methods to halt the hydration in order to study the phase transformations kinetics of such materials. In this work two methods are evaluated: use of acetone and microwave drying, aiming to withdraw the free water and inhibit further reactions. X ray diffraction and thermogravimetric tests were used to quantify the phases generated in the cement samples which were kept at 37 deg C for 1 to 15 days. The advantages and disadvantages of those procedures are presented and discussed. The use of microwave to halt the hydration process seems to be effective to withdraw the cement free water, and it can further be used in researches of the refractory castables area, endodontic cements, etc. (author)

  5. Experimental etch-and-rinse adhesives doped with bioactive calcium silicate-based micro-fillers to generate therapeutic resin-dentin interfaces.

    Science.gov (United States)

    Profeta, A C; Mannocci, F; Foxton, R; Watson, T F; Feitosa, V P; De Carlo, B; Mongiorgi, R; Valdré, G; Sauro, S

    2013-07-01

    This study aimed at evaluating the therapeutic bioactive effects on the bond strength of three experimental bonding agents containing modified Portland cement-based micro-fillers applied to acid-etched dentin and submitted to aging in simulated body fluid solution (SBS). Confocal laser (CLSM) and scanning electron microscopy (SEM) were also performed. A type-I ordinary Portland cement was tailored using different compounds such as sodium-calcium-aluminum-magnesium silicate hydroxide (HOPC), aluminum-magnesium-carbonate hydroxide hydrates (HCPMM) and titanium oxide (HPCTO) to create three bioactive micro-fillers. A resin blend mainly constituted by Bis-GMA, PMDM and HEMA was used as control (RES-Ctr) or mixed with each micro-filler to create three experimental bonding agents: (i) Res-HOPC, (ii) Res-HCPMM and (iii) Res-HPCTO. The bonding agents were applied onto 37% H3PO4-etched dentin and light-cured for 30s. After build-ups, they were prepared for micro-tensile bond strength (μTBS) and tested after 24h or 6 months of SBS storage. SEM analysis was performed after de-bonding, while CLSM was used to evaluate the ultra-morphology/nanoleakage and the mineral deposition at the resin-dentin interface. High μTBS values were achieved in all groups after 24h. Only Res-HOPC and Res-HCPMM showed stable μTBS after SBS storage (6 months). All the resin-dentin interfaces created using the bonding agents containing the bioactive micro-fillers tested in this study showed an evident reduction of nanoleakage and mineral deposition after SBS storage. Resin bonding systems containing specifically tailored Portland cement micro-fillers may promote a therapeutic mineral deposition within the hybrid layer and increase the durability of the resin-dentin bond. Copyright © 2013 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

  6. Statistical Approach for Assessing the Influence of Calcium Silicate and HPMC on the Formulation of Novel Alfuzosin Hydrochloride Mucoadhesive-Floating Beads as Gastroretentive Drug Delivery Systems

    OpenAIRE

    Fahmy, Rania Hassan

    2012-01-01

    Multiparticulate floating drug delivery systems have proven potential as controlled-release gastroretentive drug delivery systems that avoid the “all or none” gastric emptying nature of single-unit floating dosage forms. An objective of the presence investigation was to develop calcium silicate (CaSi)/calcium alginate (Ca-Alg)/hydroxypropyl methylcellulose (HPMC) mucoadhesive-floating beads that provide time- and site-specific drug release of alfuzosin hydrochloride (Alf). Beads were prepared...

  7. Copper Silicate Hydrate Hollow Spheres Constructed by Nanotubes Encapsulated in Reduced Graphene Oxide as Long-Life Lithium-Ion Battery Anode.

    Science.gov (United States)

    Wei, Xiujuan; Tang, Chunjuan; Wang, Xuanpeng; Zhou, Liang; Wei, Qiulong; Yan, Mengyu; Sheng, Jinzhi; Hu, Ping; Wang, Bolun; Mai, Liqiang

    2015-12-09

    Hierarchical copper silicate hydrate hollow spheres-reduced graphene oxide (RGO) composite is successfully fabricated by a facile hydrothermal method using silica as in situ sacrificing template. The electrochemical performance of the composite as lithium-ion battery anode was studied for the first time. Benefiting from the synergistic effect of the hierarchical hollow structure and conductive RGO matrix, the composite exhibits excellent long-life performance and rate capability. A capacity of 890 mAh/g is achieved after 200 cycles at 200 mA/g and a capacity of 429 mAh/g is retained after 800 cycles at 1000 mA/g. The results indicate that the strategy of combining hierarchical hollow structures with conductive RGO holds the potential in addressing the volume expansion issue of high capacity anode materials.

  8. 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.

  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. Copyright © 2015 John Wiley & Sons, Ltd.

  10. Hydration, hydration, hydration

    National Research Council Canada - National Science Library

    Miller, Veronica S; Bates, Graham P

    2010-01-01

    .... Although the importance of adequate hydration in combating heat stress is universally recognized, studies in a range of worker groups have demonstrated a disturbingly poor hydration level in a high...

  11. 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

  12. Silicato de cálcio como amenizante da toxidez de metais pesados em mudas de eucalipto Calcium silicate to reduce heavy metal toxicity in eucalyptus seedlings

    Directory of Open Access Journals (Sweden)

    Adriana Maria de Aguiar Accioly

    2009-02-01

    Full Text Available O objetivo deste trabalho foi avaliar o efeito do silicato de cálcio na redução da toxidez de metais pesados no solo para Eucalyptus camaldulensis. Foram utilizadas cinco doses de silicato de cálcio (0, 1,6, 3,2, 4,8 e 6,4 g kg-1, em solos com diferentes graus de contaminação. O experimento foi conduzido em vasos com 1,5 kg de solo, com uma muda por vaso, em esquema fatorial 4x5 (quatro graus de contaminação x cinco doses de silicato. O silicato de cálcio reduziu a toxidez de metais pesados em E.camaldulensis, retardou o aparecimento dos sintomas de toxidez e diminuiu os teores de zinco e cádmio na parte aérea das plantas. Entretanto, não evitou totalmente a depressão no crescimento, nos solos com contaminação elevada. O efeito amenizante do silicato foi crescente com o aumento das doses e mais evidente nos solos com contaminação elevada. O efeito benéfico do silicato de cálcio está relacionado à redução da transferência do zinco para a parte aérea do eucalipto.The objective of this study was to evaluate the effect of calcium silicate to reduce heavy metal toxicity in Eucalyptus camaldulensis seedlings. Five doses of calcium silicate (0, 1.6, 3.2, 4.8, and 6.4 g kg-1 were used in soils with increasing levels of contamination. The experiment was carried out in pots with 1.5 kg of soil, with one plant each, in a 4x5 factorial array (four levels of contamination x five silicate doses. Calcium silicate minimized heavy metal toxicity to E.camaldulensis, delayed the onset of toxicity symptoms, and decreased zinc and cadmium shoot concentrations. However, calcium silicate did not completely overcome the depressive effect upon plant growth in soils with high metal concentrations. Calcium silicate effects increased with increasing doses and were more evident in highly contaminated soils. The beneficial effects of calcium silicate on metal toxicity were highly related to the decrease in zinc translocation to the eucalyptus shoots.

  13. Comparative evaluation of calcium silicate-based dentin substitute (Biodentine?) and calcium hydroxide (pulpdent) in the formation of reactive dentin bridge in regenerative pulpotomy of vital primary teeth: Triple blind, randomized clinical trial

    OpenAIRE

    Navneet Grewal; Rubica Salhan; Nirapjeet Kaur; Hemal Bipin Patel

    2016-01-01

    Background: Considering the biological concerns of calcium hydroxide (CH) as a pulpotomy agent, an alternative silicate based dentin substitute i.e. Biodentine (Ca3SiO5) was evaluated clinically and radiographically. Aims: To evaluate the effectiveness of dentin substitute (Biodentine) in regenerative pulpotomy of vital primary teeth that would giv a biological base to its use in forming reactive dentin bridge and overcoming the drawbacks of calcium hydroxide. Material and Methods: Randomised...

  14. Identification of the Parameters of Menétrey -Willam Failure Surface of Calcium Silicate Units

    Science.gov (United States)

    Radosław, Jasiński

    2017-10-01

    The identification of parameters of Menétrey-Willamsurface made of concrete, masonry or autoclaved aerated concrete is not complicated. It is much more difficult to identify failure parameters of masonry units with cavities. This paper describes the concept of identifying the parameters of Menétrey-Willam failure surface (M-W-3) with reference to masonry units with vertical cavities. The M-W-3 surface is defined by uniaxial compressive strength fc, uniaxial tensile strength ft and eccentricity of elliptical function e. A test stand was built to identify surface parameters. It was used to test behaviour of masonry units under triaxial stress and conduct tests on whole masonry units in the uniaxial state. Results from tests on tens of silicate masonry units are presented in the Haigh-Westergaard (H-W) space. Statistical analyses were used to identify the shape of surface meridian, and then to determine eccentricity of the elliptical function.

  15. 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.

  16. The microstructure and surface morphology of radiopaque tricalcium silicate cement exposed to different curing conditions.

    Science.gov (United States)

    Formosa, L M; Mallia, B; Bull, T; Camilleri, J

    2012-05-01

    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 research was to evaluate the microstructure and surface characteristics of radiopaque tricalcium silicate cement exposed to different curing conditions namely at 100% humidity or immersed in either water or a simulated body fluid at 37°C. The materials under study included tricalcium silicate and Portland cements with and without the addition of bismuth oxide radiopacifier. Material characterization was performed on hydrated cements using a combination of scanning electron microscopy (SEM) with X-ray energy dispersive (EDX) analyses and X-ray diffraction (XRD) analyses. Surface morphology was further investigated using optical profilometry. Testing was performed on cements cured at 100% humidity or immersed in either water or Hank's balanced salt solution (HBSS) for 1 and 28 days at 37°C. In addition leachate analysis was performed by X-ray fluorescence of the storage solution. The pH of the storage solution was assessed. All the cements produced calcium silicate hydrate and calcium hydroxide on hydration. Tricalcium silicate showed a higher reaction rate than Portland cement and addition of bismuth oxide seemed to also increase the rate of reaction with more calcium silicate hydrate and calcium hydroxide being produced as demonstrated by SEM and XRD analysis and also by surface deposits viewed by the optical profilometer. Cement immersion in HBSS resulted in the deposition of calcium phosphate during the early stages following immersion and extensive calcification after 28 days. The pH of all storage solutions was alkaline. The immersion in distilled water resulted in a higher pH of the solution than when the cements were immersed in HBSS. Leachate analysis demonstrated high calcium levels in all cements tested with higher levels in tricalcium silicate and

  17. Ultrasonic sound speed of hydrating calcium sulphate hemihydrate (on-line)

    NARCIS (Netherlands)

    de Korte, A.C.J.; Brouwers, Jos

    2011-01-01

    This article focuses on the hydration, and associated microstructure development, of b-hemihydrate to dihydrate (gypsum). The sound velocity is used to quantify the composition of the fresh slurry as well as the hardening and hardened—porous—material. Furthermore, an overview of available hydration

  18. 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...... is that the cement paste structure and porosity can be engineered by addition of selected layer silicates having specific particle shapes and surface properties (e.g., charge and specific surface area). This seems to be due to the growth of calcium-silicate hydrates (C-S-H) on the clay particle surfaces......, and the nano-structure of the C-S-H depends on type of layer silicate. The effect of layer silicate addition is most pronounced for palygorskite and smectite having the largest surface area and negative charges on the particle surfaces. The cement pastes containing palygorskite and bentonite have...

  19. Preparation of the monolith of hierarchical macro-/mesoporous calcium silicate ultrathin nanosheets with low thermal conductivity by means of ambient-pressure drying.

    Science.gov (United States)

    Bai, Jilin; Li, Yuanzhi; Xiang, Jiwei; Ren, Lu; Mao, Mingyang; Zeng, Min; Zhao, Xiujian

    2015-06-01

    Calcium silicate monolith was prepared by the hydrothermal reaction of a slurry of SiO2 , calcium hydroxide, and surfactant (OP-10) obtained by high-energy ball milling, followed by drying at ambient pressure. By using this strategy, the shrinkage due to the collapse of pores during the drying of porous materials, which is a commonly observed phenomena, was successfully avoided. It has a unique microstructure of hierarchical macro-/mesoporous ultrathin calcium silicate nanosheets with a layered gyrolite crystalline structure. Very interestingly, the calcium silicate nanosheets can be peeled off to give a single-layer nanosheet (1.23 nm) of gyrolite by ultrasonication. The monolith has a low apparent density (0.073 g cm(-3) ) and low thermal conductivity (0.0399 W K(-1)  m(-1) ). The reasons behind why the formation of the unique hierarchical macro-/mesoporous ultrathin nanosheets avoids shrinkage during the hydrothermal reaction and drying, and considerably decreases the thermal conductivity, is discussed. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  20. The effect of human blood on the setting and surface micro-hardness of calcium silicate cements.

    Science.gov (United States)

    Song, Minju; Yue, Wonyoung; Kim, Soyeon; Kim, Wooksung; Kim, Yaelim; Kim, Jeong-Woong; Kim, Euiseong

    2016-11-01

    The purpose of the present study was to evaluate the effects of human blood on the setting and microhardness of calcium silicate cements. Three types of silicate-based cements were used: ProRoot MTA (PMTA), OrthoMTA (OMTA), and RetroMTA (RMTA). Mixed cement was placed into polyethylene molds with lengths of 2 and 4 mm. After storage for 4 days under three different storage conditions, i.e., saline, saline after 5 min of human blood, and human blood, the polyethylene molds were removed. With the specimens set, the surface microhardness was measured using a Vickers microhardness tester, crystalline structure was analyzed with X-ray diffraction (XRD), and the surface characteristics were examined with scanning electron microscopy (SEM). All specimens of 4 mm in length were set with all materials, and the blood groups exhibited lower microhardnesses than did the saline groups (p blood, the numbers of specimens that set were significantly different across the materials (p blood group exhibited reduced microhardness. XRD showed changes of crystalline structure in the PMTA and OMTA blood group, whereas RMTA did not. SEM analysis revealed more rounded and homogeneous structures and demonstrated a clear lack of acicular or needle-like crystals in the PMTA and OMTA blood groups, while RMTA did not reveal substantial differences between the saline- and blood-stored groups. Blood contamination detrimentally affected the surface microhardnesses of all materials; furthermore, among the 2-mm specimens, blood contamination interfered with normal setting. Therefore, RMTA might be a more suitable choice when blood contamination is unavoidable due to limited depth. Clinical relevance RetroMTA might be a more suitable choice in situations in which blood contamination is unavoidable.

  1. Polylactic acid-based porous scaffolds doped with calcium silicate and dicalcium phosphate dihydrate designed for biomedical application.

    Science.gov (United States)

    Gandolfi, Maria Giovanna; Zamparini, Fausto; Degli Esposti, Micaela; Chiellini, Federica; Aparicio, Conrado; Fava, Fabio; Fabbri, Paola; Taddei, Paola; Prati, Carlo

    2018-01-01

    Polylactic acid (PLA), dicalcium phosphate dihydrate (DCPD) and/or hydraulic calcium silicate (CaSi) have been used to prepare highly-porous scaffolds by thermally induced phase separation technique (TIPS). Three experimental mineral-doped formulations were prepared (PLA-10CaSi, PLA-5CaSi-5DCPD, PLA-10CaSi-10DCPD). Pure PLA scaffolds constituted the control group. Scaffolds were tested for their chemical-physical and biological properties, namely calcium release, alkalinizing activity, surface microchemistry and micromorphology by ESEM, apatite-forming ability by EDX, micro-Raman and IR spectroscopy, thermal properties by differential scanning calorimetry, mechanical properties by quasi-static parallel-plates compression testing, porosity by a standard water-absorption method and direct-contact cytotoxicity. All mineral-doped scaffolds released biologically relevant ions (biointeractive). A B-type carbonated apatite layer (thickness decreasing along the series PLA-10CaSi-10DCPD>PLA-10CaSi>PLA-5CaSi-5DCPD>PLA) was detected on the surface of all the 28d-aged scaffolds. Surface pores of fresh scaffolds ranged from 10 to 20μm in pure PLA to 10-100μm in PLA-10CaSi. An increase in porosity was detected in 28d-aged pure PLA scaffolds (approx. 30% of material loss with decrease of the PLA chain length); differently, in mineral-doped scaffolds, the PLA degradation was balanced by deposition/nucleation of apatite. All scaffolds showed absence of toxicity, in particular PLA-10CaSi-10DCPD. The designed scaffolds are biointeractive (release biologically relevant ions), nucleate apatite, possess high surface and internal open porosity and can be colonized by cells, appearing interesting materials for bone regeneration. Copyright © 2017 Elsevier B.V. All rights reserved.

  2. In vitro cytotoxicity of four calcium silicate-based endodontic cements on human monocytes, a colorimetric MTT assay

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    Sedigheh Khedmat

    2014-08-01

    Full Text Available Objectives This study was performed to evaluate the cytotoxicity of four calcium silicate-based endodontic cements at different storage times after mixing. Materials and Methods Capillary tubes were filled with Biodentine (Septodont, Calcium Enriched Mixture (CEM cement, BioniqueDent, Tech Biosealer Endo (Tech Biosealer and ProRoot MTA (Dentsply Tulsa Dental. Empty tubes and tubes containing Dycal were used as negative and positive control groups respectively. Filled capillary tubes were kept in 0.2 mL microtubes and incubated at 37℃. Each material was divided into 3 groups for testing at intervals of 24 hr, 7 day and 28 day after mixing. Human monocytes were isolated from peripheral blood mononuclear cells and cocultered with 24 hr, 7 day and 28 day samples of different materials for 24 and 48 hr. Cell viability was evaluated using an MTT assay. Results In all groups, the viability of monocytes significantly improved with increasing storage time regardless of the incubation time (p < 0.001. After 24 hr of incubation, there was no significant difference between the materials regarding monocyte viability. However, at 48 hr of incubation, ProRoot MTA and Biodentine were less cytotoxic than CEM cement and Biosealer (p < 0.01. Conclusions Biodentine and ProRoot MTA had similar biocompatibility. Mixing ProRoot MTA with PBS in place of distilled water had no effect on its biocompatibility. Biosealer and CEM cement after 48 hr of incubation were significantly more cytotoxic to on monocyte cells compared to ProRoot MTA and Biodentine.

  3. 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.

  4. Solubility and apical sealing characteristics of a new calcium silicate-based root canal sealer in comparison to calcium hydroxide-, methacrylate resin- and epoxy resin-based sealers.

    Science.gov (United States)

    Ersahan, Seyda; Aydin, Cumhur

    2013-01-01

    To assess and compare the water sorption, solubility and apical sealing ability of iRoot SP and three other widely used root canal sealers. Solubility was assessed by immersing standardized samples of calcium silicate- (iRoot SP), calcium hydroxide- (Sealapex), methacrylate resin- (EndoREZ) and epoxy resin- (AH Plus) based sealers in distilled water and measuring weight gain and weight loss at 6 h, 24 h and daily for 14 days. Roots of extracted mandibular premolars (n = 80) were prepared with 0.04-taper nickel-titanium rotary files to a final size 40. Roots were then randomly divided into four experimental groups (n = 18) and two control groups (n = 4), root canal sealers were applied and apical leakage was assessed using the fluid filtration method. Data was analyzed using Kruskal Wallis analysis of variance and Mann-Whitney U-tests, with the level of significance set at p ≤ 0.05. EndoREZ exhibited the highest water sorption, followed by iRoot SP, Sealapex and AH Plus. Sealapex exhibited significantly higher solubility than the other sealers, whereas no significant differences in solubility levels were observed between the other three sealers tested. AH Plus exhibited significantly lower microleakage than Sealapex and EndoREZ, whereas no difference in microleakage was found between AH Plus and iRoot SP. In view of the study findings, all tested sealers except Sealapex met the ANSI/ADA's requirements for solubility and no difference was found between AH Plus and iRoot SP in terms of apical sealing ability.

  5. Characterization of hydration products of mineral trioxide aggregate.

    Science.gov (United States)

    Camilleri, J

    2008-05-01

    To characterize the hydration products of white mineral trioxide aggregate (MTA). Mineral trioxide aggregate, white Portland cement and bismuth oxide were evaluated using X-ray diffraction (XRD) analysis and Rietveld XRD. The cements were tested un-hydrated and after hydration and curing for 30 days at 37 degrees C. Analysis of hydrated cement leachate was performed weekly for five consecutive weeks from mixing using inductively coupled plasma atomic emission spectroscopy after which the cements were viewed under the scanning electron microscope to evaluate the cement microstructure. Quantitative energy dispersive analysis with X-ray was performed and atomic ratios were plotted. Both Portland cement and MTA produced calcium silicate hydrate (C-S-H) and calcium hydroxide (CH) on hydration. The tricalcium aluminate levels were low for MTA which resulted in reduced production of ettringite and monosulphate. On hydration the bismuth level in the hydrated MTA decreased; bismuth oxide replaced the silica in the C-S-H and was leached out once the C-S-H decomposed with time. Both MTA and Portland cement released a high amount of calcium ions which decreased in amount over the 5-week period. The hydration mechanism of MTA is different to that of Portland cement. In MTA the bismuth oxide is bound to the C-S-H and is leached out from the cement with time as the C-S-H decomposes. MTA produces a high proportion of calcium ions from CH a by-product of hydration and also by decomposition of C-S-H. The release of calcium ions reduces with time.

  6. 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.

  7. Push-Out Bond Strength and Surface Microhardness of Calcium Silicate-Based Biomaterials: An in vitro Study.

    Science.gov (United States)

    Majeed, Abdul; AlShwaimi, Emad

    2017-01-01

    This was an in vitro evaluation of push-out bond strength and surface microhardness of calcium silicate-based biomaterials in coronal and apical root dentin. Ninety sections (2 mm thick) of coronal and apical root dentin were obtained from roots of 60 extracted teeth; the canals were enlarged to a standardized cavity diameter of 1.3 mm. Sections were randomly divided into 6 groups (n = 15 per group), and cavities were filled with Biodentine™, BioAggregate, or ProRoot mineral trioxide aggregate (MTA), according to the manufacturers' instructions. Push-out bond strength values were measured using a universal testing machine under a compressive load at a speed of 1 mm/min. Samples were analyzed under a light microscope to determine the nature of bond failure. Ten samples (2 mm thick) were prepared for all the materials, and Vickers microhardness was determined using a digital hardness tester. Data were analyzed using one-way analysis of variance and Tukey-Kramer multiple comparison tests at a significance level of p microhardness and BioAggregate (68.79 HV) showed the lowest hardness. Biodentine and ProRoot MTA showed higher bond strength and microhardness compared to BioAggregate. © 2016 S. Karger AG, Basel.

  8. Swelling behavior of ion exchange resins incorporated in tri-calcium silicate cement matrix: II. Mechanical analysis

    Energy Technology Data Exchange (ETDEWEB)

    Neji, M., E-mail: mejdi.neji@cea.fr [CEA, DEN, DPC, SECR, Laboratoire d' Etude du Comportement des Bétons et des Argiles, F-91191 Gif-sur-Yvette (France); Polytech Lille, LML UMR, 8107 Villeneuve d' Ascq (France); Bary, B.; Le Bescop, P. [CEA, DEN, DPC, SECR, Laboratoire d' Etude du Comportement des Bétons et des Argiles, F-91191 Gif-sur-Yvette (France); Burlion, N. [Polytech Lille, LML UMR, 8107 Villeneuve d' Ascq (France)

    2015-12-15

    This paper presents the second part of a study aiming at modelling the mechanical behavior of composites made up of ion exchange resins (IER) solidified in a tri-calcium silicate cement paste (C{sub 3}S). Such composites may be subjected to internal pressures due to ion exchange processes between ionic species which are in IER and interstitial solution of the cement paste. The reactive transport model developed in the companion paper is coupled in this study to a multi-scale approach describing the mechanical behavior of the material. It is based on an analogy with thermomechanics for taking in account the IER internal pressures, and on Eshelby-based homogenization techniques to estimate both mechanical and coupling parameters. A laboratory test has been set up to measure the macroscopic strain caused by the swelling phenomenon. The model has been finally implemented in a finite elements software. The simulation of the laboratory tests has been performed and the results have been analyzed and compared to experimental data. - Highlights: • Experimental analysis about mechanical behavior of a composite material. • Chemo-Mechanical-Transport modeling on a composite material made up with IER embedded into cement paste matrix. • Multi-scale modeling.

  9. Effects of nanosilver and nanozinc incorporated mesoporous calcium-silicate nanoparticles on the mechanical properties of dentin.

    Directory of Open Access Journals (Sweden)

    Jie Zhu

    Full Text Available Mesoporous calcium-silicate nanoparticles (MCSNs are advanced biomaterials for drug delivery and mineralization induction. They can load silver and exhibit significantly antibacterial effects. However, the effects of MCSNs and silver-loaded MCSNs on dentin are unknown. The silver (Ag and/or zinc (Zn incorporated MCSNs (Ag-Zn-MCSNs were prepared by a template method, and their characterizations were tested. Then the nanoparticles were filled into root canals and their effects on the dentin were investigated. Ag-Zn-MCSNs showed characteristics of mesoporous materials and sustained release of ions over time. Ag-Zn-MCSNs adhered well to the root canal walls and infiltrated into the dentinal tubules after ultrasound activation. Ag-Zn-MCSNs showed no significantly negative effects on either the flexural strength or the modulus of elasticity of dentin, while CH decreased the flexural strength of dentin significantly (P<0.05. These findings suggested that Ag and Zn can be incorporated into MCSNs using a template method, and the Ag-Zn-MCSNs may be developed into a new disinfectant for the root canal and dentinal tubules.

  10. Swelling behavior of ion exchange resins incorporated in tri-calcium silicate cement matrix: I. Chemical analysis

    Energy Technology Data Exchange (ETDEWEB)

    Neji, M., E-mail: mejdi.neji@cea.fr [CEA, DEN, DPC, SECR, Laboratoire d' Etude du Comportement des Bétons et des Argiles, F-91191 Gif-sur-Yvette (France); Polytech Lille – LML UMR, 8107 Villeneuve d' Ascq (France); Bary, B.; Le Bescop, P. [CEA, DEN, DPC, SECR, Laboratoire d' Etude du Comportement des Bétons et des Argiles, F-91191 Gif-sur-Yvette (France); Burlion, N. [Polytech Lille – LML UMR, 8107 Villeneuve d' Ascq (France)

    2015-12-15

    This paper presents the first part of a theoretical and experimental work aiming at modeling the chemo-mechanical behavior of composites made up of ion exchange resins (IER) solidified in a tri-calcium silicate cement paste (C{sub 3}S). Because of ion exchange processes, the volume change of the IER may cause internal pressures leading to the degradation of the material. In this study, a predictive modeling is developed for describing the chemical behavior of such material. It is based on thermodynamic equilibria to determine the evolution of the ion exchange processes, and the potential precipitation of portlandite in the composite. In parallel, a phenomenological study has been set up to understand chemical phenomena related to the swelling mechanisms. The model created has been finally implemented in a finite elements software; the simulation of a laboratory test has been performed and the results compared to experimental data. - Highlights: • Ion exchange theory to model the swelling behavior of Ion exchange resin. • Experimental phenomenon analysis about Chemo-mechanical interaction between IER and cement paste matrix. • Chemo-Transport modeling on a composite material made with IER embedded into cement paste matrix.

  11. Physicochemical Properties and Volumetric Change of Silicone/Bioactive Glass and Calcium Silicate-based Endodontic Sealers.

    Science.gov (United States)

    Tanomaru-Filho, Mario; Torres, Fernanda Ferrari Esteves; Chávez-Andrade, Gisselle Moraima; de Almeida, Madelise; Navarro, Luciana Guilherme; Steier, Liviu; Guerreiro-Tanomaru, Juliane Maria

    2017-12-01

    This study evaluated setting time (ST), radiopacity, pH, flow, solubility, and volumetric change (VC) of a silicone, gutta-percha, and bioactive glass-based sealer, GuttaFlow Bioseal (GFB), and a calcium silicate-based sealer, TotalFill BC Sealer (TFBC), in comparison with AH Plus. ST and flow were evaluated in accordance with the ISO 6876 Standard. pH was evaluated after different time intervals (1, 3, 7, 14, 21, and 28 days). Radiopacity was evaluated by radiographic analysis in millimeters of aluminum. Solubility was evaluated by means of mass loss (%) after 7 and 30 days of immersion in distilled water. VC was evaluated by micro-computed tomography, by using cavities 3 mm deep and 1 mm in diameter in acrylic resin, filled with the materials. The materials were evaluated after setting and after 7 and 30 days of immersion in distilled water. The data were submitted to analysis of variance and Tukey statistical tests (P physicochemical properties. Micro-computed tomography complements the physicochemical analysis of endodontic sealers. Copyright © 2017 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  12. Atomistic simulations of cation hydration in sodium and calcium montmorillonite nanopores

    Science.gov (United States)

    Yang, Guomin; Neretnieks, Ivars; Holmboe, Michael

    2017-08-01

    During the last four decades, numerous studies have been directed to the swelling smectite-rich clays in the context of high-level radioactive waste applications and waste-liners for contaminated sites. The swelling properties of clay mineral particles arise due to hydration of the interlayer cations and the diffuse double layers formed near the negatively charged montmorillonite (MMT) surfaces. To accurately study the cation hydration in the interlayer nanopores of MMT, solvent-solute and solvent-clay surface interactions (i.e., the solvation effects and the shape effects) on the atomic level should be taken into account, in contrast to many recent electric double layer based methodologies using continuum models. Therefore, in this research we employed fully atomistic simulations using classical molecular dynamics (MD) simulations, the software package GROMACS along with the CLAYFF forcefield and the SPC/E water model. We present the ion distributions and the deformation of the hydrated coordination structures, i.e., the hydration shells of Na+ and Ca2+ in the interlayer, respectively, for MMT in the first-layer, the second-layer, the third-layer, the fourth-layer, and the fifth-layer (1W, 2W, 3W, 4W, and 5W) hydrate states. Our MD simulations show that Na+ in Na-MMT nanopores have an affinity to the ditrigonal cavities of the clay layers and form transient inner-sphere complexes at about 3.8 Å from clay midplane at water contents less than the 5W hydration state. However, these phenomena are not observed in Ca-MMT regardless of swelling states. For Na-MMT, each Na+ is coordinated to four water molecules and one oxygen atom of the clay basal-plane in the first hydration shell at the 1W hydration state, and with five to six water molecules in the first hydration shell within a radius of 3.1 Å at all higher water contents. In Ca-MMT, however each Ca2+ is coordinated to approximately seven water molecules in the first hydration shell at the 1W hydration state and

  13. Effect of Different Irrigation Solutions on the Colour Stability of Three Calcium Silicate-Based Materials

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    Sobhnamayan F

    2017-06-01

    Full Text Available Abstract: Statement of Problem: Previous studies have shown discoloration of mineral trioxide aggregate (MTA in contact with root canal irrigation solutions. However, there are limited data on colour stability of other calcium silicate–based materials (CSMs. Objectives: This in vitro study aimed to evaluate the colour stability of three CSMs in contact with different irrigation solutions. Materials and Methods: Three CSMs including White MTA (wMTA Angelus, calcium enriched mixture (CEM, and Biodentine were assessed in this study. Forty five samples of each material were mixed according to the manufactures’ instructions and then placed in silicone tubes. After 24 hours, the materials were removed from the moulds and 9 samples of each material left dry or immersed in normal saline, 5% sodium hypochlorite (NaOCL, 2% chlorhexidinegluconate (CHX, or 17%EDTA for 24 hours. Colour changes were measured with a spectrophotometer. Data were evaluated with 2-way analysis of variance, one way analysis of variance and Tukey post hoc tests. Results: The highest discoloration of all materials was observed after contact with CHX. In the MTA Angelus and CEM cement groups, significant differences were observed between CHX and NaOCl and also between these two irrigants with the other three irrigants (p < 0.05. In the Biodentine group, CHX created statistically significant discoloration compared to other irrigants (p < 0.05. Only wMTA Angelus showed a significantly higher discoloration in contact with EDTA compared to normal saline and dry condition (p < 0.05. wMTA Angelus showed a significantly higher colour change compared with CEM cement and Biodentine after contact with NaOCl, CHX, and EDTA (p < 0.05. Conclusions: The contact of wMTA, CEM cement, and Biodentine with CHX should be avoided because this leads to severe discoloration. Contact with sodium hypochlorite also leads to discoloration of wMTA and CEM cements. Among of the three tested materials, w

  14. Fracture resistance of simulated immature teeth after apexification with calcium silicate-based materials.

    Science.gov (United States)

    Evren, O K; Altunsoy, Mustafa; Tanriver, Mehmet; Capar, Ismail Davut; Kalkan, Abdussamed; Gok, Tuba

    2016-01-01

    To compare the fracture resistance of simulated immature teeth filled with an apical barrier of mineral trioxide aggregate (MTA), Biodentine, and calcium-enriched mixture (CEM). Fifty-two single-rooted human maxillary central incisors were used. For standardization, the teeth were sectioned 6 mm above and 9 mm below the cementoenamel junction to simulate immature apex. Simulations of roots into immature apices were carried out using 1.5 mm diameter drills. The specimens were then randomly divided into three experimental groups (n = 13) and one control group (n = 13). In experimental groups, MTA, Biodentine, and CEM were placed to apical 4 mm of the simulated immature roots. The samples were stored at 37° C and 100% humidity for 1 week. A load was applied on the crown of all teeth at 135° to their long axis until fracture. The data were analyzed using one-way analysis of variance and Tukey post-hoc tests. No statistically significant differences were found among MTA, CEM, and Biodentine (P > 0.05), and these groups demonstrated higher fracture resistance than control group (P resistance of immature teeth.

  15. Vital Pulp Therapy with Calcium-Silicate Cements: Report of Two Cases.

    Science.gov (United States)

    Ashraf, Hengameh; Rahmati, Afsaneh; Amini, Neda

    2017-01-01

    This article describes successful use of calcium-enriched mixture (CEM) cement and Biodentine in apexogenesis treatment in two 8-year-old patients, one with immature permanent molar diagnosed primarily with irreversible pulpitis and the other with partially vital maxillary central incisor. After access cavity preparation, partial pulpotomy in molar and full pulpotomy in central was performed, and the remaining pulps was capped with either Biodentine or CEM cement, in each tooth. The crowns were restored with composite filling material at the following visit. The post-operative radiographic and clinical examinations (approx. average of 16 months) showed that both treated teeth remained functional, with complete root development and apex formation. A calcified bridge was produced underneath the capping material. No further endodontic intervention was necessary. Considering the healing potential of immature vital pulps, the use of CEM cement and Biodentine for apexogenesis might be an applicable choice. These new endodontic biomaterials might be appropriate for vital pulp therapies in an immature tooth. However, further clinical studies with longer follow-up periods are recommended.

  16. Solid solubility of MgO in the calcium silicates of portland clinker. The effect of CaF2

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    Puertas, F.

    1992-03-01

    Full Text Available The solid solubility of MgO in the calcium silicates of portland clinker has been determined by XRD and XDS. The influence that the presence of CaF2 has on said solubility has also been verified. The solid solution limit of MgO in C3S at 1275 ºC lies at about 1.0% wt, where the triclinic form II stabilizes. The presence of CaF2 does not alter the maximum value of the MgO solubilized in that silicate, although there does take place the stabilization of the triclinic polymorph II at lower MgO contents (between 0.3 - 0.6% wt. The maximum amount of solubilized MgO in βC2 at 1.050 ºC lies around 0.5% wt. This value does not change by the presence of CaF2.Se ha determinado por DRX y EDX la solubilidad sólida del MgO en los silicatos cálcicos del clínker portland. Se ha comprobado, así mismo la influencia que sobre dicha solubilidad tiene la presencia de CaF2. El límite de disolución sólida del MgO en el C3S a 1.275º C se sitúa alrededor del 1,0% en peso, estabilizándose la forma triclínica II. La presencia de CaF2 no altera el valor máximo de MgO solubilizado en este silicato, aunque si se produce la estabilización del polimorfo triclínico II a contenidos menores de MgO (entre 0,3 – 0,6% en peso. La cantidad máxima de MgO solubilizado en e/ βC2S a 1.050 ºC se sitúa en torno al 0,5% en peso. Este valor no se ve modificado por la presencia de CaF2.

  17. 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.

  18. Histological evaluation of tissue reactions to newly synthetized calcium silicate- and hydroxyapatite-based bioactive materials: in vivo study

    Directory of Open Access Journals (Sweden)

    Opačić-Galić Vanja

    2017-01-01

    Full Text Available Introduction/Objective. Development of materials which could be used as biological bone substitutes is one of the most valuable and active fields of biomaterial research. The goal of the study was to research the reaction of tissue on calcium silicate- (CS and hydroxyapatitebased (CS-HA newly synthesized nanomaterials, after being implanted into the subcutaneous tissue of a rats and direct pulp capping of rabbit teeth. Methods. The tested materials were implanted in 40 Wistar male rats, sacrificed after seven, 15, 30, and 60 days. The direct pulp capping was performed on the teeth of rabbits. Cavities were prepared on the vestibular surface of the incisors. The animals were sacrificed after 10 and 15 days. The control material was mineral trioxide aggregate (MTA. Histological analysis covered the tracking of inflammatory reaction cellular components, presence of gigantic cells, and necrosis of the tissue. Results. Seven days after the implantation, the strongest inflammatory response was given by the MTA (3.3 Ѓ} 0.48, while CS and CS-HA scored 3 ± 0.71. After 60 days, the rate of inflammatory reactions dropped, which was the least visible with CS-HA (0.2 ± 0.45. The least visible inflammatory reaction of the rabbits’ pulp tissue was spotted with the CS (1.83 ± 0.75, than with the MTA and CS-HA (2.67 ± 1.53, 3 ± 0.63. Conclusion. The newly synthesized materials caused a slight reaction of the subcutaneous tissue. CS-HA showed the best tissue tolerance. Nanostructural biomaterials caused a slight to moderate inflammatory reaction of the rabbits’ pulp tissue only in the immediate vicinity of the implanted material.

  19. Anticorrosive effects and in vitro cytocompatibility of calcium silicate/zinc-doped hydroxyapatite composite coatings on titanium

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Yong, E-mail: xfpang@aliyun.com [College of Lab Medicine, Hebei North University, Zhangjiakou 075000 (China); Institute of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 610054 (China); Zhang, Honglei [College of Chemistry Environmental Science, Hebei University, Baoding 071000 (China); Qiao, Haixia; Nian, Xiaofeng [College of Lab Medicine, Hebei North University, Zhangjiakou 075000 (China); Zhang, Xuejiao, E-mail: 527238610@qq.com [College of Lab Medicine, Hebei North University, Zhangjiakou 075000 (China); Wang, Wendong; Zhang, Xiaoyun; Chang, Xiaotong [College of Lab Medicine, Hebei North University, Zhangjiakou 075000 (China); Han, Shuguang [Institute of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 610054 (China); Pang, Xiaofeng [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)

    2015-12-01

    Highlights: • We developed a ZnHA/CS-coated Ti implant by using an ED method. • The obtained ZnHA/CS coatings presented a net-like micro-porous. • The ZnHA/CS coating possessed an excellent corrosion protection ability. • The composite coated CP-Ti possesses favourable cytocompatibility. - Abstract: 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 CaSiO{sub 3}. 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 Si{sup 4+} and Zn{sup 2+} 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 (Zn{sup 2+} and Si{sup 4+}). All these results indicate that ZnHA/CS composite-coated CP-Ti may be a potential material for orthopaedic applications.

  20. Synergistic acceleration in the osteogenic and angiogenic differentiation of human mesenchymal stem cells by calcium silicate-graphene composites.

    Science.gov (United States)

    Shie, Ming-You; Chiang, Wei-Hung; Chen, I-Wen Peter; Liu, Wen-Yi; Chen, Yi-Wen

    2017-04-01

    Recent exciting findings of the biological interactions of graphene materials have shed light on potential biomedical applications of graphene-containing composites. Owing to the superior mechanical properties and low coefficient of thermal expansion, graphene has been widely used in the reinforcement of biocomposites. In the present study, various ratios of graphene (0.25wt%, 0.5wt% and 1.0wt%) were reinforced into calcium silicate (CS) for bone graft application. Results show that the graphene was embedded in the composites homogeneously. Adding 1wt% graphene into CS increased the young's modulus by ~47.1%. The formation of bone-like apatite on a range of composites with graphene weight percentages ranging from 0 to 1 has been investigated in simulated body fluid. The presence of a bone-like apatite layer on the composites surface after immersion in simulated body fluid was considered by scanning electron microscopy. In vitro cytocompatibility of the graphene-contained CS composites was evaluated using human marrow stem cells (hMSCs). The proliferation and alkaline phosphatase, osteopontin and osteocalcin osteogenesis-related protein expression of the hMSCs on the 1wt% graphene-contained specimens showed better results than on the pure CS. In addition, the angiogenesis-related protein (vWF and ang-1) secretion of cells was significantly stimulated when the graphene concentration in the composites was increased. These results suggest that graphene-contained CS bone graft are promising materials for bone tissue engineering applications. Copyright © 2016. Published by Elsevier B.V.

  1. Push-Out Bond Strength and Surface Microhardness of Calcium Silicate-Based Biomaterials: An in vitro Study

    Science.gov (United States)

    Majeed, Abdul; AlShwaimi, Emad

    2017-01-01

    Objective This was an in vitro evaluation of push-out bond strength and surface microhardness of calcium silicate-based biomaterials in coronal and apical root dentin. Materials and Methods Ninety sections (2 mm thick) of coronal and apical root dentin were obtained from roots of 60 extracted teeth; the canals were enlarged to a standardized cavity diameter of 1.3 mm. Sections were randomly divided into 6 groups (n = 15 per group), and cavities were filled with Biodentine™, BioAggregate, or ProRoot mineral trioxide aggregate (MTA), according to the manufacturers' instructions. Push-out bond strength values were measured using a universal testing machine under a compressive load at a speed of 1 mm/min. Samples were analyzed under a light microscope to determine the nature of bond failure. Ten samples (2 mm thick) were prepared for all the materials, and Vickers microhardness was determined using a digital hardness tester. Data were analyzed using one-way analysis of variance and Tukey-Kramer multiple comparison tests at a significance level of p Biodentine (42.02; 39.35 MPa) and ProRoot MTA (21.86; 34.13 MPa) showed significantly higher bond strengths than BioAggregate (6.63; 10.09 MPa) in coronal and apical root dentin, respectively (p Biodentine also differed significantly from ProRoot MTA in coronal dentin. Bond failure was predominantly adhesive in Biodentine and ProRoot MTA, while BioAggregate showed predominantly mixed failure. ProRoot MTA (158.52 HV) showed significantly higher microhardness and BioAggregate (68.79 HV) showed the lowest hardness. Conclusion Biodentine and ProRoot MTA showed higher bond strength and microhardness compared to BioAggregate. PMID:27852076

  2. Effects of calcium sources and soluble silicate on bone metabolism and the related gene expression in mice.

    Science.gov (United States)

    Maehira, Fusako; Miyagi, Ikuko; Eguchi, Yukinori

    2009-05-01

    The effects of five calcium (Ca) sources were compared for bone biochemical and mechanical properties and the related gene expression using mice, from the viewpoint of their soluble silicon (Si) content. Weanling male mice were fed diets containing 1% Ca supplemented with CaCO(3) as the control (CT), coral sand (CS), fossil stony coral (FSC), fish bone (FC) and eggshell (EC) powders, and 50 ppm of Si in the CT diet for 6 mo. The mRNA expressions related to bone remodeling were quantified by real-time polymerase chain reaction. Soluble Si content was 9.83, 7.17, 2.48, 0.29, and 0.20 ppm for the CS, FC, FSC, EC, and Ca-deficient basal diets, respectively. Si, CS, and FSC, in order, significantly increased dry and ash weights, Ca and hydroxyproline contents, and alkaline phosphatase and decreased tartrate-resistant acid phosphatase and urinary excretion of hydroxyproline compared with the CT group. Si significantly increased and FC decreased femoral strength and stiffness. In the mRNA expression related to osteoblastogenesis, Si and CS significantly increased runt-related transcription factor 2. Si, CS, and FSC, in order, significantly decreased and FC and EC increased peroxisome proliferator-activated receptor-gamma. In the mRNA expression related to osteoclastogenesis, Si and CS significantly increased and FC and EC decreased the osteoprotegerin/receptor activator of nuclear factor-kappaB ligand ratio, whereas Si and CS decreased transforming growth factor-beta. The results indicated that soluble silicate and CS, with the highest Si content among Ca sources, improved bone biochemical and mechanical properties through stimulation of gene expression related to osteoblastogenesis and suppression of that related to osteoclastogenesis.

  3. Europium doped di-calcium magnesium di-silicate orange–red emitting phosphor by solid state reaction method

    Directory of Open Access Journals (Sweden)

    Ishwar Prasad Sahu

    2015-07-01

    Full Text Available A new orange–red europium doped di-calcium magnesium di-silicate (Ca2MgSi2O7:Eu3+ phosphor was prepared by the traditional high temperature solid state reaction method. The prepared Ca2MgSi2O7:Eu3+ phosphor was characterized by X-ray diffractometer (XRD, transmission electron microscopy (TEM, field emission scanning electron microscopy (FESEM with energy dispersive x-ray spectroscopy (EDX, fourier transform infrared spectra (FTIR, photoluminescence (PL and decay characteristics. The phase structure of sintered phosphor was akermanite type structure which belongs to the tetragonal crystallography with space group P4¯21m, this structure is a member of the melilite group and forms a layered compound. The chemical composition of the sintered Ca2MgSi2O7:Eu3+ phosphor was confirmed by EDX spectra. The PL spectra indicate that Ca2MgSi2O7:Eu3+ can be excited effectively by near ultraviolet (NUV light and exhibit bright orange–red emission with excellent color stability. The fluorescence lifetime of Ca2MgSi2O7:Eu3+ phosphor was found to be 28.47 ms. CIE color coordinates of Ca2MgSi2O7:Eu3+ phosphor is suitable as orange-red light emitting phosphor with a CIE value of (X = 0.5554, Y = 0.4397. Therefore, it is considered to be a new promising orange–red emitting phosphor for white light emitting diode (LED application.

  4. 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

  5. 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.

  6. A novel pharmaceutical excipient: Coprecipitation of calcium and magnesium silicate using brine-seawater in date palm cellulose as an absorbing host

    Directory of Open Access Journals (Sweden)

    Mohammad Hamaidi

    2017-09-01

    Full Text Available This research aims to produce a cost competitive and innovative pharmaceutical additive with multi-purpose use in the pharmaceutical industry from Saudi Arabia natural resources and bio-wastes. The waste substance, brine, and the naturally occurring compound, sodium silica, were reacted together to produce water insoluble calcium and magnesium silicate salts [WISS]. The purity index WISS was compared with synthetic Mg silicae.The produced particle size was 1.994 µm. Date palm cellulose [DPC] with a high purity index [0.99] was produced from the biomass waste of date palm tree. DPC was used as a host for coprecipitation of synthetic calcium magnesium silicate within its intimate structures. The interaction between the cellulose polymer and silicates is physical in nature. WISS-DPC was more flowable than DPC. In SEM, the particles of DPC were fibrous and irregular in shape, while WISS-DPC showed more regular shape than DPC. Tablets prepared from WISS-DPC were harder and had lower disintegration time at all compression forces compared to those made from DPC. The produced excipient had excellent compaction and disintegration properties and could be used as a superdisintegrant and tablet binder in pharmaceutical industries.

  7. 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)

  8. Hydration characteristics and compressive strength of hardened cement pastes containing nano-metakaolin

    Directory of Open Access Journals (Sweden)

    S.M.A. El-Gamal

    2017-04-01

    Full Text Available In this study the effect of inclusion of nano-metakaolin (NMK to ordinary Portland cement (OPC on the hydration characteristics and microstructure of hardened OPC–NMK pastes was studied. The OPC–NMK blends were prepared by the partial substitution of OPC by NMK (4, 6, 10 and 15 weight %. The fresh pastes were made using an initial water/solid (W/S ratio of 0.27 by weight and then hydrated for various time intervals. At the end of each hydration time, the hardened blended cement pastes were tested for compressive strength, free lime content, combined water content, X-ray diffraction (XRD analysis, differential scanning calorimetry (DSC and scanning electron microscopy (SEM. The compressive strength results revealed that the inclusion of nano-metakaolin into OPC improved the mechanical properties of NMK–OPC pastes during almost all ages of hydration, especially with the paste containing 10 wt% NMK. The compressive strength values obtained for OPC paste blended with 4% silica fume (SF and 6% NMK are comparable to those of the neat OPC paste. The DSC thermograms and XRD diffractograms obtained for some selected hardened pastes indicated the formation of amorphous calcium silicate hydrates, calcium sulfoaluminate hydrates, calcium aluminate hydrate and calcium hydroxide. SEM micrographs showed the formation of a dense microstructure for the hardened OPC–NMK and OPC–NMK-SF pastes as compared to the neat OPC paste after 90 days of hydration.

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

    Directory of Open Access Journals (Sweden)

    Juliane Maria GUERREIRO-TANOMARU

    Full Text Available 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 and

  10. Removal of methyl orange from aqueous solutions through adsorption by calcium aluminate hydrates.

    Science.gov (United States)

    Zhang, Ping; Wang, Tianqi; Qian, Guangren; Wu, Daishe; Frost, Ray L

    2014-07-15

    Methyl orange (MO) is a kind of anionic dye and widely used in industry. In this study, tricalcium aluminate hydrates (Ca-Al-LDHs) are used as an adsorbent to remove methyl orange (MO) from aqueous solutions. The resulting products were studied by X-ray diffraction (XRD), infrared spectroscopy (MIR), thermal analysis (TG-DTA) and scanning electron microscope (SEM). The XRD results indicated that the MO molecules were successfully intercalated into the tricalcium aluminate hydrates, with the basal spacing of Ca-Al-LDH expanding to 2.48 nm. The MIR spectrum for CaAl-MO-LDH shows obvious bands assigned to the N=N, N=H stretching vibrations and S=O, SO3(-) group respectively, which are considered as marks to assess MO(-) ion intercalation into the interlayers of LDH. The overall morphology of CaAl-MO-LDH displayed a "honey-comb" like structure, with the adjacent layers expanded. Copyright © 2014 Elsevier Inc. All rights reserved.

  11. Hydration Effects on the Stability of Calcium Carbonate Pre-Nucleation Species

    Directory of Open Access Journals (Sweden)

    Alejandro Burgos-Cara

    2017-07-01

    Full Text Available Recent experimental evidence and computer modeling have shown that the crystallization of a range of minerals does not necessarily follow classical models and theories. In several systems, liquid precursors, stable pre-nucleation clusters and amorphous phases precede the nucleation and growth of stable mineral phases. However, little is known on the effect of background ionic species on the formation and stability of pre-nucleation species formed in aqueous solutions. Here, we present a systematic study on the effect of a range of background ions on the crystallization of solid phases in the CaCO3-H2O system, which has been thoroughly studied due to its technical and mineralogical importance, and is known to undergo non-classical crystallization pathways. The induction time for the onset of calcium carbonate nucleation and effective critical supersaturation are systematically higher in the presence of background ions with decreasing ionic radii. We propose that the stabilization of water molecules in the pre-nucleation clusters by background ions can explain these results. The stabilization of solvation water hinders cluster dehydration, which is an essential step for precipitation. This hypothesis is corroborated by the observed correlation between parameters such as the macroscopic equilibrium constant for the formation of calcium/carbonate ion associates, the induction time, and the ionic radius of the background ions in the solution. Overall, these results provide new evidence supporting the hypothesis that pre-nucleation cluster dehydration is the rate-controlling step for calcium carbonate precipitation.

  12. Photo-luminescent properties of a green or red emitting Tb{sup 3+} or Eu{sup 3+} doped calcium magnesium silicate phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Onani, Martin O., E-mail: monani@uwc.ca.za [Department of Chemistry, University of the Western Cape, Private Bag X17, Bellville 7535 (South Africa); Dejene, Francis B. [Department of Physics, University of the Free State, Qwaqwa Campus, Private Bag X13, Phuthaditjhaba 9866 (South Africa)

    2014-04-15

    This study describes green-emitting Tb{sup 3+} or red-emitting Eu{sup 3+} 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 Ca{sub 2}MgSi{sub 2}O{sub 7} prepared using urea and ammonium nitrate has a tetragonal crystal structure. The resulting Tb{sup 3+}-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 Eu{sup 3+} 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 Ca{sub 2}MgSi{sub 2}O{sub 7}:Eu{sup 2+} is a broad band at 497 nm.

  13. Removal and recovery of phosphate from water by calcium-silicate composites-novel adsorbents made from waste glass and shells.

    Science.gov (United States)

    Jiang, Dan; Amano, Yoshimasa; Machida, Motoi

    2017-03-01

    The removal and recovery of phosphate from water by calcium-silicate composite (CSC) and alkali-treated calcium-silicate composite (ASC) was investigated. ASC had a higher specific surface area and total pore volume, and exhibited better performance of phosphate adsorption than CSC. In the batch mode adsorption studies, the isotherm adsorption experiments data fitted well the Langmuir isotherm model and the maximum adsorption capacities were 120 and 73.0 mg/g for ASC and for CSC, respectively. For the kinetic study, the experimental data fitted very well the pseudo-second-order kinetic model. The uptake of phosphate could be performed well over a wide pH range, from 3.0 to 13.0 for ASC and from 4.0 to 13.0 for CSC. The adsorption of phosphate by ASC was very selective even with 10 times higher concentration of other coexistent anions. For the adsorption of low phosphate concentration (10 mg/L), ASC could efficiently remove phosphate at the dosage of 0.8 g/L, while CSC was even difficult to remove phosphate at the dosage of 4.0 g/L. Phosphate fractionation results and FTIR spectra showed that phosphate-Ca complex was formed through phosphate adsorption process. The adsorbed phosphate could be successfully desorbed by 2% citric acid solution, indicating that the adsorbent after adsorbed phosphate could be reusable as fertilizer in the agricultural field.

  14. Early age hydration of calcium sulfoaluminate (synthetic ye'elimite, ) in the presence of gypsum and varying amounts of calcium hydroxide

    KAUST Repository

    Hargis, Craig W.

    2013-06-01

    Suspensions of synthetic ye\\'elimite (C4A3S̄) in a saturated gypsum (CS̄H2) and calcium hydroxide (CH) solution were examined in-situ in a wet cell by soft X-ray transmission microscopy and ex-situ by scanning electron microscopy. The most voluminous hydration product observed was ettringite. Ettringite commonly displayed acicular, filiform, reticulated, and stellate crystal habits. Additionally, pastes with C 4A3S̄, 15% CS̄H2, and varying amounts of CH were prepared and examined with X-ray diffraction (XRD) and isothermal calorimetry. The XRD experiments showed that increasing CH content caused more solid solution (SO4 2 -/OH-) AFm phases to form at early ages (< 1 d) and more monosulfate to form at later ages (> 1 d). Calorimetry indicated that the increased production of solid solution AFm was accompanied with an increase in the initial (< 30 min) rate of heat evolution, and increasing CH generally reduced the time till the second maximum rate of heat evolution due to the formation of ettringite and monosulfate. © 2013 Elsevier Ltd.

  15. Effect of Graphene Oxide (GO) on the Morphology and Microstructure of Cement Hydration Products

    Science.gov (United States)

    Zhang, Shupeng; Zheng, Dapeng; Yang, Haibin; Cui, Hongzhi; Li, Dongxu

    2017-01-01

    In this study, the effects of graphene oxide (GO) on the microstructure of cement mortars were studied using scanning electron microscopy (SEM), thermogravimetric (TG), and X-ray diffraction (XRD) techniques. Cement mortar samples with different proportions of GO (0.02, 0.04, 0.06, and 0.08 wt % based on the weight of cement) were prepared. The test results showed that GO affected the crystallization of cement hydration products, C–S–H (calcium silicate hydrate is the main hydrate product) and CH (calcium hydroxide). The morphology of hydration products changed with the increase of GO content. Furthermore, the results of XRD analyses showed that the diffraction peak intensity and the crystal grain size of CH (001), (100), (101), and (102) for GO samples increased considerably compared with the control sample. Based on the results, it can be understood that GO can modify the crystal surface of CH, leading to the formation of larger crystals. PMID:29206157

  16. Effect of Graphene Oxide (GO on the Morphology and Microstructure of Cement Hydration Products

    Directory of Open Access Journals (Sweden)

    Liguo Wang

    2017-12-01

    Full Text Available In this study, the effects of graphene oxide (GO on the microstructure of cement mortars were studied using scanning electron microscopy (SEM, thermogravimetric (TG, and X-ray diffraction (XRD techniques. Cement mortar samples with different proportions of GO (0.02, 0.04, 0.06, and 0.08 wt % based on the weight of cement were prepared. The test results showed that GO affected the crystallization of cement hydration products, C–S–H (calcium silicate hydrate is the main hydrate product and CH (calcium hydroxide. The morphology of hydration products changed with the increase of GO content. Furthermore, the results of XRD analyses showed that the diffraction peak intensity and the crystal grain size of CH (001, (100, (101, and (102 for GO samples increased considerably compared with the control sample. Based on the results, it can be understood that GO can modify the crystal surface of CH, leading to the formation of larger crystals.

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

    DEFF Research Database (Denmark)

    Lindgreen, Holger; Geiker, Mette; 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...... is that the cement paste structure and porosity can be engineered by addition of selected layer silicates having specific particle shapes and surface properties (e.g., charge and specific surface area). This seems to be due to the growth of calcium-silicate hydrates (C-S-H) on the clay particle surfaces......), surface charge, and size (micron and nano). The structure of the resulting cement pastes and mortars has been investigated by atomic force microscopy (AFM), helium porosimetry, nitrogen adsorption (specific surface area and porosity), low-temperature calorimetry (LTC) and thermal analysis. The main result...

  18. HYDRATION MECHANISMS OF CALCIUM SULPHOALUMINATE C4A3S̄ , C4AS̄ PHASE AND ACTIVE BELITE β-C2S

    Directory of Open Access Journals (Sweden)

    H. EL-DIDAMONY

    2012-12-01

    Full Text Available Highly reactive belite and calcium sulphoaluminate as well as monosulphate mix were prepared from nano-materials at lower temperatures ~1250°C. The crystal size of these materials was 25, 16 and 27 nm as determined from the X-ray analysis. The sulphoaluminate belite cement is a recent type of cement prepared at lower temperature with good properties. The aim of the present work is to synthesize C4A3S̄, monosulphate mix C4AS̄ and active belite β-C2S. The hydration mechanism was studied by XRD and DSC techniques as well as by the determination of chemically combined water contents of cement pastes with curing time. The results reveal that ettringite is first formed hydrates in the monosulphate mix, which then converted into monosulphate hydrates. The results of DSC and XRD are in good agreement with those of combined water contents. On the other side, the rate of hydration of active belite increases linearly from 3 up to 90 days, whereas, the traditional belite hydrates increase with lower rate up to 90 days, due to the thermodynamic stability structure of traditional belite.

  19. Preparation and properties of calcium-silicate filled resins for dental restoration. Part II: Micro-mechanical behaviour to primed mineral-depleted dentine.

    Science.gov (United States)

    Profeta, Andrea Corrado

    2014-11-01

    Evaluating microtensile bond strength (μTBS) and Knoop micro-hardness (KHN) of resin bonded-dentine interfaces created with two methacrylate-based systems either incorporating Bioglass 45S5 (3-E&RA/BG) or MTA (3-E&RA/WMTA). Solvated resins (50% ethanol/50% co-monomers) were used as primers while their neat counterparts were filled with the two calcium-silicate compounds. Application of neat resin adhesive with no filler served as control (3-E&RA). μTBS, KHN analysis and confocal tandem scanning microscopy (TSM) micropermeability were carried out after 24 h and 10 months of storage in phosphate buffer solution (DPBS). Scanning electron microscopy (SEM) was also performed after debonding. High μTBS values were achieved in all groups after 24 h of DPBS storage. On the contrary, solely the specimens created using 3-E&RA/BG and 3-E&RA/WMTA agents showed no significant reduction in terms of μTBS even after 10 months in DPBS; similarly, they did not restore the average superficial micro-hardness to the level of sound dentine, but maintained unchanged KHN values, and no statistical decrease was found following 10 months of DPBS storage. The only statistically significant changes occurred in the resin-dentine interfaces bonded with 3-E&RA that were subjected to a reduction of both μTBS and KHN values with ageing. In terms of micropermeability, adverse results were obtained with 3-E&RA while 3-E&RA/BG and 3-E&RA/WMTA demonstrated a beneficial effect after prolonged DPBS storage. Calcium-silicate filled composite resins performed better than a current etch-and-rinse adhesive and had a therapeutic/protective effect on the micro-mechanical properties of mineral-depleted resin-dentine interfaces. The incorporation of calcium-silicates into dental restorative and bonding agents can create more biomimetic (life-like) restorations. This will not only enable these materials to mimic the physical characteristics of the tooth structure, but will also stabilize and protect the

  20. Hydration kinetics and morphology of cement pastes with pozzolanic volcanic ash studied via synchrotron-based techniques

    Energy Technology Data Exchange (ETDEWEB)

    Kupwade-Patil, Kunal; Chin, Stephanie; Ilavsky, Jan; Andrews, Ross N.; Bumajdad, Ali; Büyüköztürk, Oral

    2017-10-13

    This study investigates the early ages of hydration behavior when basaltic volcanic ash was used as a partial substitute to ordinary Portland cement using ultra-small-angle X-ray scattering and wide-angle X-ray scattering (WAXS). The mix design consisted of 10, 30 and 50% substitution of Portland cement with two different-sized volcanic ashes. The data showed that substitution of volcanic ash above 30% results in excess unreacted volcanic ash, rather than additional pozzolanic reactions along longer length scales. WAXS studies revealed that addition of finely ground volcanic ash facilitated calcium-silicate-hydrate related phases, whereas inclusion of coarser volcanic ash caused domination by calcium-aluminum-silicate-hydrate and unreacted MgO phases, suggesting some volcanic ash remained unreacted throughout the hydration process. Addition of more than 30% volcanic ash leads to coarser morphology along with decreased surface area and higher intensity of scattering at early-age hydration. This suggests an abrupt dissolution indicated by changes in surface area due to the retarding gel formation that can have implication on early-age setting influencing the mechanical properties of the resulting cementitious matrix. The findings from this work show that the concentration of volcanic ash influences the specific surface area and morphology of hydration products during the early age of hydration. Hence, natural pozzolanic volcanic ashes can be a viable substitute to Portland cement by providing environmental benefits in terms of lower-carbon footprint along with long-term durability.

  1. Atributos químicos de solos influenciados pela substituição do carbonato por silicato de cálcio Soil chemical properties influenced by the substitution of calcium carbonate by calcium silicate

    Directory of Open Access Journals (Sweden)

    Renato Ferreira de Souza

    2008-08-01

    ácia do silicato de Ca foi inferior à de carbonato de Ca na melhoria das condições químicas do solo.The application of silicates to soils can result in increased soil cation exchange capacity (CEC, displace anions, especially H2PO4- (diacid phosphate, neutralize the pH and Al toxicity and, in general, increase the nutrient availability to plants. However, calcium silicates may be less efficient than calcium carbonates. To evaluate the effect of calcium carbonate substitution by calcium silicate on the soil chemical properties, especially on phosphorus availability, four experiments were conducted in an entirely randomized design with four replications, in a greenhouse. The treatments consisted of five levels (0, 25, 50, 75, and 100 % of calcium carbonate substitution by calcium silicate, with a 4:1 Ca:Mg stoichiometric and the same amount of CaO, enough to reach a 60 % base saturation. The treatments were applied to 4 dm³ samples of a sandy orthic Quartzarenic Neosol (Quartzpsament, a sandy loam dystrophic Red-Yellow Latosol (Oxisol, sandy clay loam dystrophic Red-Yellow Latosol (Oxisol and a clayey dystrophic Red Latosol (Oxisol; each soil represented one experiment. The pH values in H2O, P, phosphorus in the equilibrium solution (P-rem, K, Ca, Mg, Si, Al, H + Al, organic matter (OM, Cu, Mn, Zn and B, sum of bases (S, effective (t ant total (T CEC, base saturation (V and Al saturation (m were submitted to analysis of variance and simple regression models fitted as a function of CaCO3 substitution by CaSiO3 levels. It was observed that carbonate substitution by silicate promoted significant increases in the values of Si, Al, H + Al and m and reduction in the values of P-rem, pH, S, t and V. The values of Mehlich 1 P, K, Mg, OM, T, Mn, Cu, and B were not influenced significantly. A reduction in Zn availability was verified in the dystrophic orthic Quartzarenic Neosol only. Calcium silicate was less efficient than calcium carbonate in the improvement of soil chemical

  2. Calcium

    Science.gov (United States)

    ... Turn to calcium-fortified (or "calcium-set") tofu, soy milk, tempeh, soy yogurt, and cooked soybeans (edamame). Calcium-fortified foods. Look for calcium-fortified orange juice, soy or rice milk, breads, and cereal. Beans. You can get decent ...

  3. The role of integrin αv in proliferation and differentiation of human dental pulp cell response to calcium silicate cement.

    Science.gov (United States)

    Hung, Chi-Jr; Hsu, Hsin-I; Lin, Chi-Chang; Huang, Tsui-Hsien; Wu, Buor-Chang; Kao, Chia-Tze; Shie, Ming-You

    2014-11-01

    It has been proved that integrin αv activity is related to cell proliferation, differentiation, migration, and organ development. However, the biological functions of integrin αv in human dental pulp cells (hDPCs) cultured on silicate-based materials have not been explored. The aim of this study was to investigate the role of integrin αv in the proliferation and odontogenic differentiation of hDPCs cultured with the effect of calcium silicate (CS) cement and β-tricalcium phosphate (TCP) cement. In this study, hDPCs were cultured on CS and TCP materials, and we evaluated fibronectin (FN) secretion and integrin αv expression during the cell attachment stage. After small interfering RNA transfection targeting integrin αv, the proliferation and odontogenesis differentiation behavior of hDPCs were analyzed. The results indicate that CS releases Si ion-increased FN secretion and adsorption, which promote cell attachment more effectively than TCP. The CS cement facilitates FN and αv subintegrin expression. However, the FN adsorption and integrin expression of TCP are similar to that observed in the control dish. Integrin αv small interfering RNA inhibited odontogenic differentiation of hDPCs with the decreased formation of mineralized nodules on CS. It also down-regulated the protein expression of multiple markers of odontogenesis and the expression of dentin sialophosphoprotein protein. These results establish composition-dependent differences in integrin binding and its effectiveness as a mechanism regulating cellular responses to biomaterial surface. Copyright © 2014 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  4. A combined QXRD/TG method to quantify the phase composition of hydrated Portland cements

    Energy Technology Data Exchange (ETDEWEB)

    Soin, Alexander V.; Catalan, Lionel J.J. [Department of Chemical Engineering, Lakehead University, 955 Oliver Road, Thunder Bay, Ontario P7B 5E1 (Canada); Kinrade, Stephen D., E-mail: stephen.kinrade@lakeheadu.ca [Department of Chemistry, Lakehead University, 955 Oliver Road, Thunder Bay, Ontario P7B 5E1 (Canada)

    2013-06-15

    A new method is reported for quantifying the mineral phases in hydrated cement pastes that is based on a combination of quantitative X-ray diffractometry (QXRD) and thermogravimetry (TG). It differs from previous methods in that it gives a precise measure of the amorphous phase content without relying on an assumed stoichiometric relationship between the principal hydration products, calcium hydroxide (CH) and calcium silicate hydrate (C–S–H). The method was successfully applied to gray and white ordinary Portland cements (GOPC and WOPC, respectively) that were cured for up to 56 days. Phase distributions determined by QXRD/TG closely matched those from gray-level analysis of backscattered scanning electron microscope (BSEM) images, whereas elemental compositions obtained for the amorphous phase by QXRD/TG agreed well with those measured by quantitative energy dispersive X-ray spectroscopy (EDS)

  5. Thermochemistry of Calcium-Magnesium-Aluminum-Silicate (CMAS) and Components of Advanced Thermal and Environmental Barrier Coating Systems

    Science.gov (United States)

    Costa, Gustavo C. C.; Acosta, Waldo A.; Zhu, Dongming; Ghoshal, Anindya

    2017-01-01

    There is increasing interest in the degradation mechanism studies of thermal and environmental barrier coatings (TEBCs) of gas turbines by molten CaO-MgO-Al(exp. 2)O(exp. 3)-SiO(exp. 2) CMAS). CMAS minerals are usually referred as silicon-containing sand dust and volcano ash materials that are carried by the intake air into gas turbines, e.g. in aircraft engines, and their deposits often react at high temperatures (greater than 1200 degrees C) with the engine turbine coating systems and components. The high temperature reactions causes degradation and accelerated failure of the static and rotating components of the turbine engines. We discuss some results of the reactions between the CMAS and Rare-Earth (RE = Y, Yb, Dy, Gd, Nd and Sm) - oxide stabilized ZrO(exp. 2) or HfO(exp. 2) systems, and the stability of the resulting oxides and silicates. Plasma sprayed hollow tube samples (outside diameter = 4.7 mm, wall thickness = 0.76 mm and = 26 mm height) were half filled with CMAS powder, wrapped and sealed with platinum foil, and heat treated at 1310 degrees C for 5h. Samples were characterized by differential scanning calorimetry (DSC), X-ray diffraction, and cross-section electron microscopy analysis and energy dispersive X-ray spectroscopy. It was found that CMAS penetrated the samples at the grain boundaries and dissolved the TEBC materials to form silicate phases containing the rare-earth elements. Furthermore, it was found that apatite crystalline phases were formed in the samples with total rare-earth content higher than 12 mol% in the reaction zone for the ZrO(exp. 2) system. In general, samples with the nominal compositions (30YSZ), HfO(exp. 2)-7Dy(exp. 2)O(exp. 2) and ZrO(exp. 2)-9.5Y(exp. 2)O(exp. 3)-2.25Gd(exp. 2)O(exp. 3)-2.25Yb(exp. 2)O(exp. 3) exhibited lower reactivity or more resistance to CMAS than the other coating compositions of this work.

  6. Sealing ability of a new calcium silicate based material as a dentin substitute in class II sandwich restorations: An in vitro study

    Directory of Open Access Journals (Sweden)

    Raji Viola Solomon

    2014-01-01

    Full Text Available Background: Class ll sandwich restorations are routinely performed where conventional Glass ionomer cement (GIC or Resin-modified GIC (RMGIC is used as a base or dentin substitute and a light curing composite resin restorative material is used as an enamel substitute. Various authors have evaluated the microleakage of composite resin restorations where glass ionomer cement has been used as a base in class II sandwich restorations, but a literature survey reveals limited studies on the microleakage analysis of similar restorations with biodentine as a dentin substitute, as an alternative to glass ionomer cement. The aim of this study is: To evaluate the marginal sealing efficacy of a new calcium-silicate-based material (Biodentine as a dentin substitute, at the cervical margins, in posterior class II sandwich restorations.To compare and evaluate the microleakage at the biodentine/composite interface with the microleakage at the resin-modified GIC/composite interface, in posterior class II open sandwich restorations. To compare the efficacy between a water-based etch and rinse adhesive (Scotch bond multipurpose and an acetone-based etch and rinse adhesive (Prime and bond NT, when bonding biodentine to the composite. To evaluate the enamel, dentin, and interfacial microleakage at the composite and biodentine/RMGIC interfaces. Materials and Methods: Fifty class II cavities were prepared on the mesial and distal surfaces of 25 extracted human maxillary third molars, which were randomly divided into five groups of ten cavities each: (G1 Biodentine group, (G2 Fuji II LC GIC group, (G3 Biodentine as a base + prime and bond NT + Tetric N-Ceram composite, (G4 Biodentine + scotchbond multi-purpose + Tetric N-Ceram composite, (G5 Fuji II LC as a base + prime and bond NT+ Tetric-N Ceram composite. The samples were then subjected to thermocycling, 2500× (5°C to 55°C, followed by the dye penetration test. Scores are given from 0 to 3 based on the depth of

  7. 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 ...

  8. Comparative evaluation of calcium silicate-based dentin substitute (Biodentine® and calcium hydroxide (pulpdent in the formation of reactive dentin bridge in regenerative pulpotomy of vital primary teeth: Triple blind, randomized clinical trial

    Directory of Open Access Journals (Sweden)

    Navneet Grewal

    2016-01-01

    Full Text Available Background: Considering the biological concerns of calcium hydroxide (CH as a pulpotomy agent, an alternative silicate based dentin substitute i.e. Biodentine (Ca3SiO5 was evaluated clinically and radiographically. Aims: To evaluate the effectiveness of dentin substitute (Biodentine in regenerative pulpotomy of vital primary teeth that would giv a biological base to its use in forming reactive dentin bridge and overcoming the drawbacks of calcium hydroxide. Material and Methods: Randomised clinical trial on 40 bilateral carious primary molars in 20 participant children (aged 5-10 years was carried out by same operator using Ca3SiO5(group-1 and CH (group-2 as vital pulpotomy agents. Blinded clinical and radiographic outcomes were observed at 3, 6 and 12 months interval. Results: Clinical outcomes of both protocols were analysed using Pearson's chi-square test applied at P < 0.05. Descriptive statistics were expressed as mean increase in dentin bridge formation in mms from two reference points in standardized radiographs using paired 't'- test at baseline and 12 months and found to be statistically significant (P < 0.05 in group-1 when compared with group-2. Conclusion: Group-1 revealed statistically favourable regenerative potential along with clinical success compared to group 2 thereby sharing both indications and mode of action with CH, but without its drawbacks of physical and clinical properties.

  9. Comparative evaluation of calcium silicate-based dentin substitute (Biodentine®) and calcium hydroxide (pulpdent) in the formation of reactive dentin bridge in regenerative pulpotomy of vital primary teeth: Triple blind, randomized clinical trial.

    Science.gov (United States)

    Grewal, Navneet; Salhan, Rubica; Kaur, Nirapjeet; Patel, Hemal Bipin

    2016-01-01

    Considering the biological concerns of calcium hydroxide (CH) as a pulpotomy agent, an alternative silicate based dentin substitute i.e. Biodentine (Ca3SiO5) was evaluated clinically and radiographically. To evaluate the effectiveness of dentin substitute (Biodentine) in regenerative pulpotomy of vital primary teeth that would giv a biological base to its use in forming reactive dentin bridge and overcoming the drawbacks of calcium hydroxide. Randomised clinical trial on 40 bilateral carious primary molars in 20 participant children (aged 5-10 years) was carried out by same operator using Ca3SiO5(group-1) and CH (group-2) as vital pulpotomy agents. Blinded clinical and radiographic outcomes were observed at 3, 6 and 12 months interval. Clinical outcomes of both protocols were analysed using Pearson's chi-square test applied at P < 0.05. Descriptive statistics were expressed as mean increase in dentin bridge formation in mms from two reference points in standardized radiographs using paired 't'- test at baseline and 12 months and found to be statistically significant (P < 0.05) in group-1 when compared with group-2. Group-1 revealed statistically favourable regenerative potential along with clinical success compared to group 2 thereby sharing both indications and mode of action with CH, but without its drawbacks of physical and clinical properties.

  10. Comparative evaluation of calcium silicate-based dentin substitute (Biodentine®) and calcium hydroxide (pulpdent) in the formation of reactive dentin bridge in regenerative pulpotomy of vital primary teeth: Triple blind, randomized clinical trial

    Science.gov (United States)

    Grewal, Navneet; Salhan, Rubica; Kaur, Nirapjeet; Patel, Hemal Bipin

    2016-01-01

    Background: Considering the biological concerns of calcium hydroxide (CH) as a pulpotomy agent, an alternative silicate based dentin substitute i.e. Biodentine (Ca3SiO5) was evaluated clinically and radiographically. Aims: To evaluate the effectiveness of dentin substitute (Biodentine) in regenerative pulpotomy of vital primary teeth that would giv a biological base to its use in forming reactive dentin bridge and overcoming the drawbacks of calcium hydroxide. Material and Methods: Randomised clinical trial on 40 bilateral carious primary molars in 20 participant children (aged 5-10 years) was carried out by same operator using Ca3SiO5(group-1) and CH (group-2) as vital pulpotomy agents. Blinded clinical and radiographic outcomes were observed at 3, 6 and 12 months interval. Results: Clinical outcomes of both protocols were analysed using Pearson's chi-square test applied at P < 0.05. Descriptive statistics were expressed as mean increase in dentin bridge formation in mms from two reference points in standardized radiographs using paired ‘t’- test at baseline and 12 months and found to be statistically significant (P < 0.05) in group-1 when compared with group-2. Conclusion: Group-1 revealed statistically favourable regenerative potential along with clinical success compared to group 2 thereby sharing both indications and mode of action with CH, but without its drawbacks of physical and clinical properties. PMID:27994411

  11. Statistical approach for assessing the influence of calcium silicate and HPMC on the formulation of novel alfuzosin hydrochloride mucoadhesive-floating beads as gastroretentive drug delivery systems.

    Science.gov (United States)

    Fahmy, Rania Hassan

    2012-09-01

    Multiparticulate floating drug delivery systems have proven potential as controlled-release gastroretentive drug delivery systems that avoid the "all or none" gastric emptying nature of single-unit floating dosage forms. An objective of the presence investigation was to develop calcium silicate (CaSi)/calcium alginate (Ca-Alg)/hydroxypropyl methylcellulose (HPMC) mucoadhesive-floating beads that provide time- and site-specific drug release of alfuzosin hydrochloride (Alf). Beads were prepared by simultaneous internal and external gelation method utilizing 3(2) factorial design as an experimental design; with two main factors evaluated for their influence on the prepared beads; the concentration of CaSi as floating aid (X (1)) and the percentage of HPMC as viscosity enhancer and mucoadhesive polymer (X (2)), each of them was tested in three levels. Developed formulations were evaluated for yield, entrapment efficiency, particle size, surface topography, and buoyancy. Differential scanning calorimetry, Fourier transform infrared spectroscopy, in vitro drug release, as well as in vitro mucoadhesion using rat stomach mucosal membrane were also conducted. Percentage yield and entrapment efficiency ranged from 57.03% to 78.51% and from 49.78% to 83.26%, respectively. Statistical analysis using ANOVA proved that increasing the concentration of either CaSi or HPMC significantly increased the beads yield. Both CaSi and HPMC concentrations were found to significantly affect Alf release from the beads. Additionally, higher CaSi concentration significantly increased the beads diameter while HPMC concentration showed significant positive effect on the beads mucoadhesive properties. CaSi/Ca-Alg/HPMC beads represent simple floating-mucoadhesive gastroretentive system that could be useful in chronopharmacotherapy of benign prostatic hyperplasia.

  12. Combined effect of magnesia and zirconia on the bioactivity of calcium silicate ceramics at C\\S ratio less than unity.

    Science.gov (United States)

    Ewais, Emad M M; Amin, Amira M M; Ahmed, Yasser M Z; Ashor, Eman A; Hess, Ulrike; Rezwan, Kurosch

    2017-01-01

    This paper describes the effect of magnesia in the presence of zirconia on the bioactivity, microstructure and physico-mechanical properties of calcium silicate composition adjusted at calcia/silica ratio(C/S) of 0.5. A mixture from calcium carbonate and silica was conducted at C/S of 0.5. 20wt.% of magnesia and 5-25wt.% of ZrO2 were added. Each mixture was mixed with ethanol in a planetary ball mill, dried, formed and fired at a temperature of 1325±5°C. Phase composition, FE-SEM, and physico-mechanical properties of the fired specimens were determined and explained. The in vitro bioactivities of these specimens were investigated by analysis of their abilities to form apatite in the simulated body fluid (SBF) for a short time (7days) using SEM-EDS. The findings indicated that the surface of the specimens containing 5 and 15wt.% ZrO2 were completely covered by single and multilayered hydroxyapatite (HA) precipitate typical to "cauliflower" morphology, respectively. The surface of the specimen containing 25wt.% ZrO2 did not cover, but there are some scattered HA precipitate. The differences among the results were rationalized based on the phase composition. Vickers hardness and fracture toughness of the specimens of highly promised bioactivity were 2.32-2.57GPa and 1.80-1.50MPa. m(1/2), respectively. The properties of these specimens are similar to the properties of human cortical bone. Consequently, these composites might be used as bone implant materials. Copyright © 2016 Elsevier B.V. All rights reserved.

  13. Evaluation of cytocompatibility of calcium silicate-based endodontic sealers and their effects on the biological responses of mesenchymal dental stem cells.

    Science.gov (United States)

    Rodríguez-Lozano, F J; García-Bernal, D; Oñate-Sánchez, R E; Ortolani-Seltenerich, P S; Forner, L; Moraleda, J M

    2017-01-01

    To investigate in vitro the cytocompatibility of the calcium silicate-containing endodontic sealers MTA Fillapex and TotalFill BC Sealer on human periodontal ligament stem cells (hPDLSCs) by assaying their biological responses and compare them with that observed when using an epoxy resin-based sealer (AH Plus). Specimens from the three different endodontic sealers were eluated with culture medium for 24 h. The cytotoxicity of these eluates was evaluated using the MTT assay. In addition, an in vitro scratch wound healing model was used to determine their effects on cell migration. Cell adhesion to collagen type I after treatment with the different sealer eluates was also measured, whereas cytotoxicity was determined using the DNA-specific fluorochrome Hoechst 33342. Finally, to assess cell morphology and attachment to the different sealers, hPDLSCs were directly seeded onto the material surfaces and analysed by scanning electron microscopy (SEM). One-way analysis of variance (anova) followed by a Bonferroni post-test were performed (P Endodontic Journal. Published by John Wiley & Sons Ltd.

  14. Clinical and radiographic comparison of indirect pulp treatment using light-cured calcium silicate and mineral trioxide aggregate in primary molars: A randomized clinical trial

    Science.gov (United States)

    Menon, Navya P.; Varma, Balagopal R.; Janardhanan, Sureshkumar; Kumaran, Parvathy; Xavier, Arun Mamachan; Govinda, Bhat Sangeetha

    2016-01-01

    Aim: To clinically and radiographically evaluate the reparative dentin formation in indirect pulp treatment (IPT) using mineral trioxide aggregate (MTA) and light cured calcium silicate (TheraCal) in primary molars over a period of 6 months. Materials and Methods: A clinical trial on IPT on 43 primary molars in 21 patients between the age of 4–7 years, divided into two groups: 22 teeth in MTA group and 21 in TheraCal group. Measurement of the variation in dentin thickness was done on the digitalized radiograph at baseline, 3 months and 6 months using CorelDRAW X3 software. Results: Statistical analysis using an independent t-test for intragroup and intergroup comparison showed a significant increase in dentin thickness in both the MTA and TheraCal group (intragroup comparison [P MTA and TheraCal showed no statistical difference in reparative dentin formation (P > 0.05). Conclusion: Clinically and radiographically, both MTA and TheraCal are good IPT materials. The better handling characteristics and comparable reparative dentin-forming ability of TheraCal make this material an alternative to MTA in pediatric restorative procedures. PMID:27994414

  15. Evaluation and Comparison of Occurrence of Tooth Discoloration after the Application of Various Calcium Silicate-based Cements: An Ex Vivo Study.

    Science.gov (United States)

    Shokouhinejad, Noushin; Nekoofar, Mohammad H; Pirmoazen, Salma; Shamshiri, Ahmad R; Dummer, Paul M H

    2016-01-01

    Biodentine (Septodont, Saint Maur des Fossés, France), OrthoMTA (BioMTA, Seoul, Korea), and EndoSequence Root Repair Material (ERRM; Brasseler, Savannah, GA) have been developed to overcome the shortcomings of mineral trioxide aggregate (MTA). The purpose of this study was to compare tooth discoloration after the application of ProRoot MTA (Dentsply Tulsa Dental Products, Tulsa, OK) and 3 recently introduced calcium silicate-based cements in the presence and absence of blood. In total, 104 human anterior teeth were prepared; 96 were randomly divided into 2 groups (blood and saline contamination). Each group was subdivided into 4 experimental subgroups (n = 12) of ProRoot MTA, Biodentine, OrthoMTA, and ERRM that were used to fill the pulp chambers. The remaining 8 teeth served as the saline and blood groups. Color analysis of tooth crowns was performed using a spectroradiometer before the application of materials and at 24 hours, 1 month, and 6 months after application. Repeated measures analysis of variance was used to evaluate the effects of blood, material, and time on color change (ΔE*). Tooth color change in all experimental groups increased over time (P discolorations with materials in the presence of blood. However, in the absence of blood, Biodentine and ERRM exhibited less tooth discoloration than OrthoMTA. Copyright © 2016 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  16. Influences of mesoporous zinc-calcium silicate on water absorption, degradability, antibacterial efficacy, hemostatic performances and cell viability to microporous starch based hemostat.

    Science.gov (United States)

    Hou, Yu; Xia, Yan; Pan, Yongkang; Tang, Songchao; Sun, Xiaofei; Xie, Yang; Guo, Han; Wei, Jie

    2017-07-01

    Efficacious hemostatic agents have significant potential application in visceral organ or large vessel arterial injure. In this study, mesoporous zinc-calcium silicate (m-ZCS) was synthesized, and microporous starch (MS) based hemostatic agents of m-ZCS/MS composites for hemorrhage control was fabricated. The results showed that the incorporation of m-ZCS into MS significantly enhanced the water absorption and degradability of the composites, which were dependent on the m-ZCS content. Moreover, the composites with antibacterial property could inhibit the growth of Escherichia coli (E. coli) and the antibacterial ratios increased with the m-ZCS content. The in vitro coagulation evaluation by using activated partial thromboplastin time (APTT) and prothrombin time (PT) revealed that the composites significantly activated the intrinsic and extrinsic pathway of coagulation cascade. In addition, for the animal model of rabbits in ear vein, skin, arterial and liver injuries, the hemostatic time of the composites obviously reduced with the increase of m-ZSC content, in which the composite with 15wt% m-ZCS content (15mZSC) showed remarkable efficacy on bleeding control. The composites could promote the viability of L929 cells, indicating no cytotoxicity of the composites. The results suggested that the m-ZCS/MS composites with excellent hemostatic and antibacterial properties might be a candidate for controlling bleeding and infection. Copyright © 2017. Published by Elsevier B.V.

  17. 3D printed scaffolds of calcium silicate-doped β-TCP synergize with co-cultured endothelial and stromal cells to promote vascularization and bone formation.

    Science.gov (United States)

    Deng, Yuan; Jiang, Chuan; Li, Cuidi; Li, Tao; Peng, Mingzheng; Wang, Jinwu; Dai, Kerong

    2017-07-17

    Synthetic bone scaffolds have potential application in repairing large bone defects, however, inefficient vascularization after implantation remains the major issue of graft failure. Herein, porous β-tricalcium phosphate (β-TCP) scaffolds with calcium silicate (CS) were 3D printed, and pre-seeded with co-cultured human umbilical cord vein endothelial cells (HUVECs) and human bone marrow stromal cells (hBMSCs) to construct tissue engineering scaffolds with accelerated vascularization and better bone formation. Results showed that in vitro β-TCP scaffolds doped with 5% CS (5%CS/β-TCP) were biocompatible, and stimulated angiogenesis and osteogenesis. The results also showed that 5%CS/β-TCP scaffolds not only stimulated co-cultured cells angiogenesis on Matrigel, but also stimulated co-cultured cells to form microcapillary-like structures on scaffolds, and promoted migration of BMSCs by stimulating co-cultured cells to secrete PDGF-BB and CXCL12 into the surrounding environment. Moreover, 5%CS/β-TCP scaffolds enhanced vascularization and osteoinduction in comparison with β-TCP, and synergized with co-cultured cells to further increase early vessel formation, which was accompanied by earlier and better ectopic bone formation when implanted subcutaneously in nude mice. Thus, our findings suggest that porous 5%CS/β-TCP scaffolds seeded with co-cultured cells provide new strategy for accelerating tissue engineering scaffolds vascularization and osteogenesis, and show potential as treatment for large bone defects.

  18. 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.

  19. Cinética de hidratação de ligantes à base de alumina hidratável ou aluminato de cálcio Kinetics of hydration of binders based on hydratable alumina or calcium aluminate cement

    Directory of Open Access Journals (Sweden)

    I. R. Oliveira

    2007-03-01

    Full Text Available O estado de dispersão da matriz de um concreto refratário apresenta uma grande influência no comportamento reológico desse material, determinando as técnicas utilizadas para a sua aplicação. Tais métodos normalmente exigem a preparação de concretos com elevada fluidez, que possam ser bombeados com facilidade e sejam capazes de preencher moldes de formato complexo sem a necessidade de aplicação de vibração. Entretanto, embora tais requisitos favoreçam uma boa trabalhabilidade do concreto, tendem a aumentar o tempo requerido para efetuar a desmoldagem do corpo conformado. Uma vez que o desenvolvimento da resistência mecânica do concreto está intimamente relacionado ao processo de hidratação do ligante hidráulico, este necessita ser controlado quando se busca a redução do tempo para a desmoldagem. Tal controle depende de um profundo conhecimento das variáveis que determinam a cinética das reações. Neste contexto, o objetivo deste trabalho foi o de avaliar a influência do tipo de ligante hidráulico, da temperatura e da presença de finos (matriz ou de aditivos inorgânicos adicionados ao concreto sobre o processo de hidratação por meio de medidas de temperatura e ensaios reológicos oscilatórios em função do tempo.The dispersion of refractory castables matrix presents a great influence on their rheological behavior, which defines the most appropriate methods for placing these materials. The growing demand for automatically transported refractory castables has promoted the use of pumpable castables, usually specified as self flow compositions. Nevertheless, castables with higher fluidity present longer workability, leading to extended demoulding times. Because the strength development is intimately linked to the hydration process of calcium aluminate cement or hydratable alumina, it needs to be controlled in order to reach the minimum time for demoulding, contributing to reducing overall costs. The control of cement

  20. Calcium isotopic fractionation in mantle peridotites by melting and metasomatism and Ca isotope composition of the Bulk Silicate Earth

    Science.gov (United States)

    Kang, Jin-Ting; Ionov, Dmitri A.; Liu, Fang; Zhang, Chen-Lei; Golovin, Alexander V.; Qin, Li-Ping; Zhang, Zhao-Feng; Huang, Fang

    2017-09-01

    To better constrain the Ca isotopic composition of the Bulk Silicate Earth (BSE) and explore the Ca isotope fractionation in the mantle, we determined the Ca isotopic composition of 28 peridotite xenoliths from Mongolia, southern Siberia and the Siberian craton. The samples are divided in three chemical groups: (1) fertile, unmetasomatized lherzolites (3.7-4.7 wt.% Al2O3); (2) moderately melt-depleted peridotites (1.3-3.0 wt.% Al2O3) with no or very limited metasomatism (LREE-depleted cpx); (3) strongly metasomatized peridotites (LREE-enriched cpx and bulk rock) further divided in subgroups 3a (harzburgites, 0.1-1.0% Al2O3) and 3b (fertile lherzolites, 3.9-4.3% Al2O3). In Group 1, δ44/40Ca of fertile spinel and garnet peridotites, which experienced little or no melting and metasomatism, show a limited variation from 0.90 to 0.99‰ (relative to SRM 915a) and an average of 0.94 ± 0.05‰ (2SD, n = 14), which defines the Ca isotopic composition of the BSE. In Group 2, the δ44/40Ca is the highest for three rocks with the lowest Al2O3, i.e. the greatest melt extraction degrees (average 1.06 ± 0.04 ‰, i.e. ∼0.1‰ heavier than the BSE estimate). Simple modeling of modal melting shows that partial melting of the BSE with 103 ln ⁡αperidotite-melt ranging from 0.10 to 0.25 can explain the Group 2 data. By contrast, δ44/40Ca in eight out of nine metasomatized Group 3 peridotites are lower than the BSE estimate. The Group 3a harzburgites show the greatest δ44/40Ca variation range (0.25-0.96‰), with δ44/40Ca positively correlated with CaO and negatively correlated with Ce/Eu. Chemical evidence suggests that the residual, melt-depleted, low-Ca protoliths of the Group 3a harzburgites were metasomatized, likely by carbonate-rich melts/fluids. We argue that such fluids may have low (≤0.25‰) δ44/40Ca either because they contain recycled crustal components or because Ca isotopes, similar to trace elements and their ratios, may be fractionated by kinetic and

  1. Calcium

    Science.gov (United States)

    ... and blood vessels contract and expand, to secrete hormones and enzymes and to send messages through the nervous system. It is important to get plenty of calcium in the foods you eat. Foods rich in calcium include Dairy products such as milk, cheese, and yogurt Leafy, green vegetables Fish with ...

  2. Mechanical and physical behavior of newly developed functionally graded materials and composites of stainless steel 316L with calcium silicate and hydroxyapatite.

    Science.gov (United States)

    Ataollahi Oshkour, Azim; Pramanik, Sumit; Mehrali, Mehdi; Yau, Yat Huang; Tarlochan, Faris; Abu Osman, Noor Azuan

    2015-09-01

    This study aimed to investigate the structural, physical and mechanical behavior of composites and functionally graded materials (FGMs) made of stainless steel (SS-316L)/hydroxyapatite (HA) and SS-316L/calcium silicate (CS) employing powder metallurgical solid state sintering. The structural analysis using X-ray diffraction showed that the sintering at high temperature led to the reaction between compounds of the SS-316L and HA, while SS-316L and CS remained intact during the sintering process in composites of SS-316L/CS. A dimensional expansion was found in the composites made of 40 and 50 wt% HA. The minimum shrinkage was emerged in 50 wt% CS composite, while the maximum shrinkage was revealed in samples with pure SS-316L, HA and CS. Compressive mechanical properties of SS-316L/HA decreased sharply with increasing of HA content up to 20 wt% and gradually with CS content up to 50 wt% for SS-316L/CS composites. The mechanical properties of the FGM of SS-316L/HA dropped with increase in temperature, while it was improved for the FGM of SS-316L/CS with temperature enhancement. It has been found that the FGMs emerged a better compressive mechanical properties compared to both the composite systems. Therefore, the SS-316L/CS composites and their FGMs have superior compressive mechanical properties to the SS-316L/HA composites and their FGMs and also the newly developed FGMs of SS-316L/CS with improved mechanical and enhanced gradation in physical and structural properties can potentially be utilized in the components with load-bearing application. Copyright © 2015 Elsevier Ltd. All rights reserved.

  3. Evaluation of the filling ability of artificial lateral canals using calcium silicate-based and epoxy resin-based endodontic sealers and two gutta-percha filling techniques.

    Science.gov (United States)

    Fernández, R; Restrepo, J S; Aristizábal, D C; Álvarez, L G

    2016-04-01

    To evaluate the ability of a calcium silicate-based sealer (iRoot SP) and an epoxy resin-based sealer (Topseal) using two gutta-percha filling techniques to fill artificial lateral canals (ALCs). Seventy single-rooted human teeth were selected. Ten of these were used to obtain pilot data. Three ALCs were produced on mesial and distal surfaces of each root, one in each third, using size 10 engine reamers. The roots were randomly assigned to four experimental groups according to the filling technique and sealer used: 1, cold gutta-percha (single-point technique) with iRoot SP (SP-iR); 2, cold gutta-percha (single-point technique) with Topseal (SP-T); 3, continuous wave of condensation technique with iRoot SP (CWC-iR); and 4, continuous wave of condensation technique with Topseal (CWC-T). Digital periapical radiographs were taken. After the sealer had set, the roots were demineralized, cleared in methyl-salicylate and examined under a stereomicroscope. The depth of penetration of sealer and/or gutta-percha into the ALC was scored using a 5-point system, conducting an analysis on four surfaces. Filling scores of 0-1 were considered not acceptable, whilst scores of 2-4 were considered acceptable. Pearson's chi-square test was used to compare the experimental groups (P epoxy resin-based sealer with both filling techniques was effective in artificial filling lateral canals. © 2015 International Endodontic Journal. Published by John Wiley & Sons Ltd.

  4. A Comparison in Mechanical Properties of Cermets of Calcium Silicate with Ti-55Ni and Ti-6Al-4V Alloys for Hard Tissues Replacement

    Directory of Open Access Journals (Sweden)

    Azim Ataollahi Oshkour

    2014-01-01

    Full Text Available This study investigated the impact of calcium silicate (CS content on composition, compressive mechanical properties, and hardness of CS cermets with Ti-55Ni and Ti-6Al-4V alloys sintered at 1200°C. The powder metallurgy route was exploited to prepare the cermets. New phases of materials of Ni16Ti6Si7, CaTiO3, and Ni31Si12 appeared in cermet of Ti-55Ni with CS and in cermet of Ti-6Al-4V with CS, the new phases Ti5Si3, Ti2O, and CaTiO3, which were emerged during sintering at different CS content (wt%. The minimum shrinkage and density were observed in both groups of cermets for the 50 and 100 wt% CS content, respectively. The cermets with 40 wt% of CS had minimum compressive Young’s modulus. The minimum of compressive strength and strain percentage at maximum load were revealed in cermets with 50 and 40 wt% of CS with Ti-55Ni and Ti-6Al-4V cermets, respectively. The cermets with 80 and 90 wt% of CS showed more plasticity than the pure CS. It concluded that the composition and mechanical properties of sintered cermets of Ti-55Ni and Ti-6Al-4V with CS significantly depend on the CS content in raw cermet materials. Thus, the different mechanical properties of the cermets can be used as potential materials for different hard tissues replacements.

  5. Retreatability of three calcium silicate-containing sealers and one epoxy resin-based root canal sealer with four different root canal instruments.

    Science.gov (United States)

    Donnermeyer, David; Bunne, Clarissa; Schäfer, Edgar; Dammaschke, Till

    2017-06-22

    The objective of the study was to compare the retreatability of three calcium silicate-containing sealers (BioRoot RCS, MTA Fillapex, Endo C.P.M.) and an epoxy resin-based sealer (AH Plus) with different root canal instruments (Hedström files, Reciproc R40, Mtwo retreatment file R 25/.05 + Mtwo 40/.06, and F6 SkyTaper) concerning sealer remnants and retreatment time. Root canals of 192 teeth were instrumented with Reciproc R40. All root canals were obturated using the single-cone technique with Reciproc R40 gutta-percha and one of the sealers (n = 48 per sealer). Two months later, retreatment was performed using one of the mentioned instruments (n = 12 per instrument and sealer). The roots were split longitudinally, and both halves were investigated using light microscopy. The percentage of sealer remnants covering the root canal wall was evaluated using the software ImageJ. The time required for retreatment was recorded. Statistical analysis was performed using two-way ANOVA and Student-Newman-Keuls post hoc test. Regarding the percentage of root canal filling remnants as well as retreatment time, two-way ANOVA indicated that the results were significantly affected by the sealer (p instrument used (p instruments allowed significantly faster retreatment than the other instruments (p instruments was superior compared to hand instrumentation. Engine-driven NiTi instruments are better suited to remove root canal fillings than stainless steel Hedström files.

  6. 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

  7. Calcium

    Science.gov (United States)

    ... from dietary supplements are linked to a greater risk of kidney stones, especially among older adults. But calcium from foods does not appear to cause kidney stones. For most people, other factors (such as not drinking enough fluids) probably have ...

  8. Obtaining calcium silicates by using solid residues as precursors. Influence of water in the process of mixing reagents; Obtencin de silicatos de calcio empleando como precursores residuos solidos. Influencia del mezclado de reactivos en fase seca o fase humeda

    Energy Technology Data Exchange (ETDEWEB)

    Felipe-Sese, M.; Eliche-Quesada, D.; Corpas-Iglesias, F. A.

    2011-07-01

    The suitability of re-using residues marble, remaining from cutting marble, as a source of calcium-oxide, as well as the resultant ashes from the combustion of the wastes generated in the process of manufacturing boards from derivates of wood, as a source of silica, as raw material for the production of calcium silicate products has been determined. First of all, the influence of water has been studied in the initial phase of mixing residues. Marble and ashes have been mixed in molar relation CaO:SiO{sub 2} of 1:1 using two different ways: using a planetary ball mill (while in solid state) or agitating at 90 degree centigrade (2 h) using a 60 wt% of water (while in humid state). Later, both mixtures were sintered at 1100 degree centigrade (24 h). In order to use the obtained calcium-silicates as ceramic insulating thermal materials, the samples were compressed at 15 Tm obtaining bricks from which the technological properties have been studied. The ceramic materials obtained from mixing the residues in dry phase, as well as those obtained in the wet phase, can be used as thermal insulators, showing values of conductivity of 0.18 and 0.12 w/m{sup 2}K, with an elevated resistance to compressive strength. (Author) 14 refs.

  9. Sorption Mechanisms of Eu(3+) on CSH Phases of Hydrated Cements.

    Science.gov (United States)

    Pointeau, Ingmar; Piriou, Bernard; Fedoroff, Michel; Barthes, Marie-Genevieve; Marmier, Nicolas; Fromage, Francine

    2001-04-15

    The sorption mechanisms of Eu(3+) on calcium silicate hydrate (CSH) phases of hydrated cement were investigated as a tool for the prediction of the behavior of trivalent radionuclides with aged/degraded cements in radioactive waste repositories. Four techniques were used: site-selective and time-resolved luminescence spectroscopy, XPS, high-resolution SEM coupled with EDX, and XRD. Results showed that europium is not precipitated in the solution despite its low solubility limit. It is strongly retained on CSH, resulting in a more than 99.8% sorption rate. Two main sorption sites were characterized by luminescence spectroscopy. One site, with a long lifetime, can be interpreted as Eu included in the framework of CSH. Another one, with a shorter lifetime, can be interpreted as a site with a hydrated environment that is high but is less than that of europium hydroxide. It corresponds to superficial complexation or precipitation. Copyright 2001 Academic Press.

  10. Development of novel tricalcium silicate-based endodontic cements with sintered radiopacifier phase.

    Science.gov (United States)

    Xuereb, M; Sorrentino, F; Damidot, D; Camilleri, Josette

    2016-06-01

    All implants, bone and endodontic cements need to be sufficiently radiopaque to be able to be distinguished from neighbouring anatomical structures post-operatively. For this purpose, radiopacifying materials are added to the cements to render them sufficiently radiopaque. Bismuth oxide has been quite a popular choice of radiopacifier in endodontic materials. It has been shown to cause dental discoloration. The aim of this study was to develop, characterize and assess the properties of tricalcium silicate cement with alternative radiopacifiers, which are either inter-ground or sintered to the tricalcium silicate cement. Custom-made endodontic cements based on tricalcium silicate and 20 % barium, calcium or strontium zirconate, which were either inter-ground or sintered at high temperatures, were produced. The set materials stored for 28 days in Hank's balanced salt solution were characterized by scanning electron microscopy and X-ray diffraction analysis. Assessment of pH, leaching, interaction with physiological solution, radiopacity, setting time, compressive strength and material porosity were investigated. Mineral trioxide aggregate (MTA) Angelus was used as control. Addition of radiopacifying materials improved the radiopacity of the material. The sintered cements exhibited the formation of calcium zirconate together with the respective radiopacifier phase. All materials produced calcium hydroxide on hydration, which interacted with tissue fluids forming hydroxyapatite on the material surface. The physical properties of the tricalcium silicate-based cements were comparable to MTA Angelus. A novel method of producing radiopaque tricalcium silicate-based cements was demonstrated. The novel materials exhibited properties, which were either comparable or else improved over the control. The novel materials can be used to replace MTA for root-end filling, perforation repair and other clinical applications where MTA is indicated.

  11. Influência da escória silicatada na acidez do solo e na produtividade de grãos do arroz de terras altas Influence of calcium silicate slag on soil acidity and upland rice grain yield

    Directory of Open Access Journals (Sweden)

    Morel Pereira Barbosa Filho

    2004-04-01

    Full Text Available Apesar dos elevados teores de SiO2 total geralmente encontrados nos solos brasileiros, o teor na solução do solo pode ser baixo, em conseqüência do processo de dessilicificação que ocorre durante a intemperização dos solos. A aplicação de escórias de processamento industrial, ricas em silicatos de cálcio, tem mostrado efeitos positivos quanto à ação corretiva da acidez do solo e ao fornecimento de Si às plantas acumuladoras desse elemento, com aumentos significativos de produtividade. Conduziu-se este trabalho com o seguinte objetivo: avaliar em dois anos de cultivo sucessivos a ação corretiva, a produtividade de grãos e a absorção de Si pelo arroz de terras altas. Foram aplicadas ao solo de cerrado classificado como latossolo vermelho distroférrico de cerrado seis doses (0, 2, 4, 6, 8 e 10 t ha-1 de uma escória silicatada com 20% de SiO2 total, proveniente do processo de fabricação de superfosfatos em forno elétrico. Utilizou-se o delineamento de blocos completos casualizados com cinco repetições. Foram detectados aumentos significativos de produtividade de grãos, teor e acumulação de Si na palha e da porcentagem de grãos cheios por panícula, nos dois anos de cultivo do arroz. Houve ação corretiva no solo das doses de escória, reduzindo a acidez e aumentando a disponibilidade de P, Si, Ca trocável e a porcentagem de saturação por bases. O nível crítico de Si na palha por ocasião da colheita, para obtenção de produtividade satisfatória de grãos, foi estabelecido em 2,25 g kg-1 de matéria seca.Despite the high SiO2 total content often found in Brazilian soils, the soluble silicon content in soil solution can be low due to weathering that occur in soils. The application of calcium silicate slags, under these conditions, has demonstrated positive effects in relation to correction of soil acidity, the supply of Si to plants that accumulate this element and significant yield increase. The objectives of

  12. Hydration kinetics for the alite, belite, and calcium aluminate phase in Portland cements from 27Al and 29Si MAS NMR spectroscopy

    DEFF Research Database (Denmark)

    Skibsted, Jørgen; Jensen, Ole Mejlhede; Jakobsen, Hans Jørgen

    1997-01-01

    29Si magic-angle spinning (MAS) NMR spectroscopy is shown to be a valuable tool for obtaining the quantities of alite and belite in hydrated Portland cements. The hydration (1-180 days) of a white Portland cement with 10 wt.% silica fume added is investigated and the degrees of hydration for alit...

  13. Studying the Hydration of a Retarded Suspension of Ground Granulated Blast-Furnace Slag after Reactivation

    Science.gov (United States)

    Schneider, Nick; Stephan, Dietmar

    2016-01-01

    This article presents a combined use of a retarder (d-gluconic acid) and an alkaline activator (sodium hydroxide) in a binder system based on ground granulated blast-furnace slag. The properties of the retarder are extending the dormant hydration period and suppressing the generation of strength-giving phases. Different retarder concentrations between 0.25 and 1.00 wt.% regulate the intensity and the period of the retardation and also the characteristics of the strength development. The activator concentration of 30 and 50 wt.% regulates the overcoming of the dormant period and thereby the solution of the slag and hence the formation of the hydration products. The research objective is to produce a mineral binder system based on two separate liquid components. The highest concentration of retarder and activator generates the highest compressive strength and mass of hydration products—after 90 days of hydration a compressive strength of more than 50 N/mm2. The main phases are calcium silicate hydrate and hydrotalcite. Generally, the combination of retarder and activator shows a high potential in the performance increase of the hydration process. PMID:28774054

  14. Studying the Hydration of a Retarded Suspension of Ground Granulated Blast-Furnace Slag after Reactivation

    Directory of Open Access Journals (Sweden)

    Nick Schneider

    2016-11-01

    Full Text Available This article presents a combined use of a retarder (d-gluconic acid and an alkaline activator (sodium hydroxide in a binder system based on ground granulated blast-furnace slag. The properties of the retarder are extending the dormant hydration period and suppressing the generation of strength-giving phases. Different retarder concentrations between 0.25 and 1.00 wt.% regulate the intensity and the period of the retardation and also the characteristics of the strength development. The activator concentration of 30 and 50 wt.% regulates the overcoming of the dormant period and thereby the solution of the slag and hence the formation of the hydration products. The research objective is to produce a mineral binder system based on two separate liquid components. The highest concentration of retarder and activator generates the highest compressive strength and mass of hydration products—after 90 days of hydration a compressive strength of more than 50 N/mm2. The main phases are calcium silicate hydrate and hydrotalcite. Generally, the combination of retarder and activator shows a high potential in the performance increase of the hydration process.

  15. 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.

  16. Interaction of dispersed polyvynil acetate with silicate in finishing materials

    Directory of Open Access Journals (Sweden)

    Runova, R. F.

    1996-12-01

    Full Text Available This article focuses on the processes of interaction between calcium silicate hydrates and dispersed polyvinyl acetate in tight films with the aim of developing compounds meant for restoration and finishing works. The basis of this development relies on the concept concerning the determining role of the crystal-chemical factor of the silicate phase in the formation of organic-mineral compounds of increased durability. The characteristics of dispersed calcium silicate hydrates are portrayed. The preparation conditions, accounting for the synthesis of the product of submicrocrystalline structure, conforming with the stoichiometry CaO∙SiO2 =0.8-2.0 have been determined. The interaction has been studied for compounds achieved by mixing ingredients in a rapid whirling mixer, and subjected to hardening at T=20+2 T. With the aid of XRD, DTA and Infra-Red Spectrometry methods the formation process of the sophisticated polymer silicate phase in the material was observed for a period of 90 days. The properties of the film were investigated and its high resistance against the influence of external factors was established. On this basis a conclusion concerning the quite high effectiveness of substituting portland cement with dispersed calcium silicate hydrate in polymer cement compounds has been made. White colour and other various special properties determine the suitability for repair and finishing works on facades of buildings.

    Este artículo está orientado a estudiar los procesos de interacción entre los silicatos cálcicos hidratados y el acetato de polivinilo disperso en capas impermeables, con el objeto de desarrollar compuestos destinados para la restauración. El fundamento de estos estudios es determinar el papel que los factores cristaloquímicos de las fases silicato tienen en la formación de compuestos órganominerales de elevada durabilidad. Se han descrito las características de los silicatos cálcicos hidratados

  17. Calcium and potassium silicates and the growth of Eucalyptus grandis seedlings Aplicação de silicatos de cálcio e de potássio e o crescimento de mudas de Eucalyptus grandis

    Directory of Open Access Journals (Sweden)

    Itamar Antonio Bognola

    2011-06-01

    Full Text Available

    The use of silicate is a practice that has been frequently adopted in annual crops, although few studies have been conducted in order to verify its efficiency in forest tree species. The main objective of this research was to evaluate the effect of calcium and potassium silicates in the growth of seedlings of Eucalyptus grandis. The experiment was conducted in a greenhouse, in Alambari county, State of São Paulo. A completely randomized experimental design was adopted, with eight treatments, three replications and 25 plants per plot, maintained at the field capacity moisture level. Seedlings were planted in plastic tubes using local substrate, basic fertilization and silicates. Diameter, height and fresh and dry biomass of the seedlings were determined 150 days after silicates treatments were applied. The use of silicates either in the substrate or through foliar application, in the production of eucalypt seedlings has proven to be inadequate when the substrate presents a balanced basic composition in terms of nutrients and pH.

    doi: 10.4336/2011.pfb.31.66.83

    O uso de silicato é uma prática que vem sendo adotada com frequência em culturas anuais, muito embora poucos trabalhos tenham sido realizados com intuito de verificar sua eficiência em espécies florestais arbóreas. O objetivo principal desta pesquisa foi avaliar o efeito da aplicação de silicatos de cálcio e de potássio no crescimento de mudas de Eucalyptus grandis. O experimento foi conduzido em casa de vegetação, no Município de Alambari, SP. O delineamento usado foi inteiramente ao acaso, com oito tratamentos, três repetições e 25 plantas por parcela, sendo mantidas na umidade de capacidade de campo. As mudas foram plantadas em tubetes de plástico, utilizando substrato local, com adubação básica e silicatos. Diâmetro de colo, altura e biomassa verde e seca das mudas foram determinados 150 dias após a

  18. 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.

  19. Hydration lubrication

    National Research Council Canada - National Science Library

    Klein, Jacob

    2013-01-01

    The hydration lubrication paradigm, whereby hydration layers are both strongly held by the charges they surround, and so can support large pressures without being squeezed out, and at the same time...

  20. Avaliação de cultivares de alface adubadas com silicato de cálcio em casa-de-vegetação Evaluation of lettuce cultivars fertilized with calcium silicate in greenhouse

    Directory of Open Access Journals (Sweden)

    Regina Lúcia Félix Ferreira

    2010-10-01

    Full Text Available O experimento foi conduzido no Departamento de Ciência do Solo da Universidade Federal de Lavras - UFLA, no período de junho a agosto de 2002. Objetivou-se avaliar a produtividade, o estado nutricional e a qualidade (classe de tamanho de cultivares de alface cultivadas com doses de silicato de cálcio em vasos sob casa-de-vegetação. O delineamento experimental foi em blocos casualizados, com quatro repetições, com 1 planta/vaso, em esquema fatorial 3 x 4 + 3, sendo três cultivares de alface (Raider, Regina e Vera e quatro doses de silicato de cálcio (0, 410, 1,000 e 2,000 mg dm-3; os tratamentos adicionais foram compostos pela aplicação de 820 mg dm-3 de carbonato de cálcio, para as três cultivares. O estado nutricional das plantas de alface foi avaliado pelo Sistema Integrado de Diagnose e Recomendação (DRIS. A aplicação da fonte silicato de cálcio não aumentou o crescimento das plantas e não aumentou o teor dos nutrientes nas plantas de alface, mas melhorou a nutrição das plantas para Si e aumentou a porcentagem de plantas sadias. A aplicação também aumentou a concentração de Mn, devido ao alto conteúdo de Mn no fertilizante aplicado (Silifértil®. As três variedades de alface comportaram-se como plantas não acumuladoras de Si.The experiment was carried out at the Department of Soil Sciences of the Universidade Federal de Lavras - UFLA, from June to August 2002, with the objective to evaluate the productivity, the nutritional state and the quality (size class of lettuce cultivars grown with calcium silicate in greenhouse. The experimental design was disposed in blocks with four replicates, in factorial arrangement with additional treatments: 3 x 4 +3, composed by three lettuce cultivars: Raider (group crisphead lettuce; Regina (group butterhead lettuce and Vera (group looseleaf lettuce and four calcium silicate rates (0, 410, 1.000 and 2.000 mg dm-3, additional treatments were composed of the application of

  1. Static demolition by calcium oxide. Part 3. Hydration properties of calcium oxide which is varied on its surface by CO2 gas flow; Seisekkai wo shuseibun to suru seiteki hasaizai. 3. Seisekkai ryushi no hyoso kaishitsu ni yoru suiwa kyodo

    Energy Technology Data Exchange (ETDEWEB)

    Fukui, H. [ROX Japan Co. Ltd., Tokyo (Japan); Tsugeno, S.; Nagaishi, T. [Kyushu Sangyo University, Fukuoka (Japan). Faculty of Engineering

    1998-10-31

    Fast granular type static demolition agent is dominated by solid-phase surface hydration reaction, and its local hydration velocity is remarkably accelerated on solid surfaces. In some cases, such phenomena cause work defects such as boiling of hydration water and eruption of the agent by pressurized vapor. Study was made on reduction of an initial hydration velocity through surface modification by direct reaction of CO2 with CaO powder. As a result, CaCO3 with thin layer calcite structure was formed on surfaces, modifying surfaces. In dry hydration (equimolar) of modified CaO, the hydration velocity was remarkably reduced, and the utmost exothermic temperature was also lowered. A water diffusion velocity into CaO was affected and reduced probably by formation of surface carbonate layers. Jander` formula was applied as rate-determining formula of diffusion on surface reactive layers to analyze the initial stage of hydration. As the analysis result under the assumption that formation of modified layers is proportional to treatment times, it was estimated that the initial stage of hydration of CaO treated by CO2 is controlled by 1-D diffusion of water into surface CaCO3 layers. 6 refs., 12 figs., 2 tabs.

  2. Characterization of silicates and calcium carbonates applied to high-dose dosimetry; Caracterizacao de silicatos e carbonatos de calcio aplicados a dosimetria de doses altas

    Energy Technology Data Exchange (ETDEWEB)

    Vila, Gustavo Barreto

    2012-07-01

    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 {sup 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 Mn{sup 2+} in the coral and mother-of-pearl samples before irradiation. In the case of the irradiated samples, the defects found were CO{sub 2}{sup -}, CO{sub 3}{sup 3-}, CO{sub 3}{sup -} and SO{sub 2}{sup -}, 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

  3. Alleviating negative effects of irrigation-water salinity on growth and vase life of gerbera by foliar spray of calcium chloride and potassium silicate

    OpenAIRE

    A. Mohammadi Torkashvand

    2015-01-01

    The required water for greenhouses in Kishestan, Soume-e-Sara town, Guilan province, Iran, is mainly provided by underground resources that have inappropriate quality. One way to reduce the impact of salinity an plant growth is proper nutrition. This greenhouse research was conducted to evaluate the effect of water salinity and foliar spray of calcium (Ca) and silicon (Si) on growth and vase life of gerbera in a factorial experiment based on compeletly randomized design with two factors. The ...

  4. The influence of Al{sub 2}O{sub 3}, MgO and ZnO on the crystallization characteristics and properties of lithium calcium silicate glasses and glass-ceramics

    Energy Technology Data Exchange (ETDEWEB)

    Salman, S.M. [Glass Research Department, National Research Centre, El-Behoos St., Dokki, Cairo (Egypt)], E-mail: saadmoghazy@hotmail.com; Darwish, H.; Mahdy, E.A. [Glass Research Department, National Research Centre, El-Behoos St., Dokki, Cairo (Egypt)

    2008-12-20

    The crystallization characteristics of glasses based on the Li{sub 2}O-CaO-SiO{sub 2} eutectic (954 {+-} 4 deg. C) system containing Al{sub 2}O{sub 3}, MgO and ZnO has been investigated by differential thermal analysis (DTA), X-ray diffraction analysis (XRD), and scanning electron microscopy (SEM). The partial replacement of Li{sub 2}O by Al{sub 2}O{sub 3} and CaO by MgO or ZnO in the studied glass-ceramics led to the development of different crystalline phase assemblages, including lithium meta- and di-silicates, lithium calcium silicates, {alpha}-quartz, diopside, clinoenstatite, wollastonite, {beta}-eucryptite ss, {beta}-spodumene, {alpha}-tridymite, lithium zinc orthosilicate, hardystonite and willemite using various heat-treatment processes. The dilatometric thermal expansion of the glasses and their corresponding glass-ceramics were determined. A wide range of thermal expansion coefficient values were obtained for the investigated glasses and their corresponding crystalline products. The thermal expansion coefficients of the investigated glasses were decreased by Al{sub 2}O{sub 3}, MgO or ZnO additions. The {alpha}-values of the investigated glasses were ranged from (+18) to (+108) x 10{sup -7} K{sup -1} (25-300 deg. C), while those of the glass-ceramics were (+3) to (+135) x 10{sup -7} K{sup -1} (25-700 deg. C). The chemical durability of the glass-ceramics, towards the attack of 0.1N HCl solution, was markedly improved by Al{sub 2}O{sub 3} with MgO replacements. The composition containing 11.5 mol% Al{sub 2}O{sub 3} and 6.00 mol% MgO exhibited low thermal expansion values and good chemical durability.

  5. A new quantification method based on SEM-EDS to assess fly ash composition and study the reaction of its individual components in hydrating cement paste

    Energy Technology Data Exchange (ETDEWEB)

    Durdziński, Paweł T., E-mail: pawel.durdzinski@gmail.com [Laboratory of Construction Materials, École Polytechnique Fédérale de Lausanne (EPFL), Station 12, CH-1015 Lausanne (Switzerland); Dunant, Cyrille F. [Laboratory of Construction Materials, École Polytechnique Fédérale de Lausanne (EPFL), Station 12, CH-1015 Lausanne (Switzerland); Haha, Mohsen Ben [HeidelbergCement Technology Center GmbH (HeidelbergCement AG), Rohrbacher Str. 95, 69181 Leimen (Germany); Scrivener, Karen L. [Laboratory of Construction Materials, École Polytechnique Fédérale de Lausanne (EPFL), Station 12, CH-1015 Lausanne (Switzerland)

    2015-07-15

    Calcareous fly ashes are high-potential reactive residues for blended cements, but their qualification and use in concrete are hindered by heterogeneity and variability. Current characterization often fails to identify the dominant, most reactive, amorphous fraction of the ashes. We developed an approach to characterize ashes using electron microscopy. EDS element composition of millions of points is plotted in a ternary frequency plot. A visual analysis reveals number and ranges of chemical composition of populations: silicate, calcium-silicate, aluminosilicate, and calcium-rich aluminosilicate. We quantified these populations in four ashes and followed their hydration in two Portland-ash systems. One ash reacted at a moderate rate: it was composed of 70 vol.% of aluminosilicates and calcium-silicates and reached 60% reaction at 90 days. The other reacted faster, reaching 60% at 28 days due to 55 vol.% of calcium-rich aluminosilicates, but further reaction was slower and 15 vol.% of phases, the silica-rich ones, did not react.

  6. Effect of calcium and magnesium silicate on the growth of the castor oil plant subjected to salinity levels
    Efeito de silicato de cálcio e magnésio sobre o crescimento de plantas de mamoneira submetidas a níveis de salinidade

    OpenAIRE

    José Félix Brito Neto; Napoleão de Esberard Macêdo Beltrão; João Paulo Gonsiorkiewicz Rigon; Silvia Capuani

    2012-01-01

    Salt stress decreases the osmotic potential of soil solution causing water stress, causing toxic effects in the plants resulting in injuries on the metabolism and nutritional disorders, thus compromising the plant growth, resulting in lower production. The calcium silicate and magnesium can perform the same function as limestone, besides providing silicon to plants, may also contribute to the resistance of plants to salt stress. Thus, the objective of this study was to evaluate the effect of ...

  7. Hydration characteristics of zirconium oxide replaced Portland cement for use as a root-end filling material.

    Science.gov (United States)

    Camilleri, J; Cutajar, A; Mallia, B

    2011-08-01

    Zirconium oxide can be added to dental materials rendering them sufficiently radiopaque. It can thus be used to replace the bismuth oxide in mineral trioxide aggregate (MTA). Replacement of Portland cement with 30% zirconium oxide mixed at a water/cement ratio of 0.3 resulted in a material with adequate physical properties. This study aimed at investigating the microstructure, pH and leaching in physiological solution of Portland cement replaced zirconium oxide at either water-powder or water-cement ratios of 0.3 for use as a root-end filling material. The hydration characteristics of the materials which exhibited optimal behavior were evaluated. Portland cement replaced by zirconium oxide in varying amounts ranging from 0 to 50% in increments of 10 was prepared and divided into two sets. One set was prepared at a constant water/cement ratio while the other set at a constant water/powder ratio of 0.3. Portland cement and MTA were used as controls. The materials were analyzed under the scanning electron microscope (SEM) and the hydration products were determined. X-ray energy dispersive analysis (EDX) was used to analyze the elemental composition of the hydration products. The pH and the amount of leachate in Hank's balanced salt solution (HBSS) were evaluated. A material that had optimal properties that satisfied set criteria and could replace MTA was selected. The microstructure of the prototype material and Portland cement used as a control was assessed after 30 days using SEM and atomic ratio diagrams of Al/Ca versus Si/Ca and S/Ca versus Al/Ca were plotted. The hydration products of Portland cement replaced with 30% zirconium oxide mixed at water/cement ratio of 0.3 were calcium silicate hydrate, calcium hydroxide and minimal amounts of ettringite and monosulphate. The calcium hydroxide leached in HBSS solution resulted in an increase in the pH value. The zirconium oxide acted as inert filler and exhibited no reaction with the hydration by-products of Portland

  8. Cement hydration inhibition and crosslinking in the guar-borate system

    Science.gov (United States)

    Bishop, Maximilienne

    The hydration of cement and its individual mineral phases in the presence of different inhibitors has been investigated. The behavior of an exemplary oligo-phosphate, nitriltris(methylene)phosphonic acid (H6ntmp), is compared to the behavior of more traditional retarders. The reaction between H6ntmp and calcium hydroxide, tricalcium silicate, tricalcium aluminate, and cement have revealed that the calcium phosphonate complex, [Ca(H 4ntmp)]infinity, plays a role in inhibition with phosphonates. NMR and XPS data suggest that the presence of uncoordinated P-O bonds in calcium phosphonates lends phosphonates the unique ability to simultaneously complex calcium ions while adhering to hydrating aluminate surfaces, promoting heterogeneous nucleation of calcium phosphonates at the surface of aluminate minerals and blocking normal hydration reactions. Reactions with tartaric acid also forms a calcium complex on top of the aluminate phases. In contrast, sucrose, appears to act directly on the silicate phases actually accelerates the reactions of the aluminate phases. The reactions of borate ions with diols and monosaccharides have been used to model cross-linking in the guar-borate system. Specifically, the reactions of borate with alcohols were characterized by 11B NMR to determine which reactions are most favorable. It was found that the acidity of the hydroxyl groups plays an important role in the efficiency of cross-linking, and has a greater effect on the energy of the resulting borate-diol complexes than the conformation (i.e., cis versus trans) in reactions of borate with cyclohexanediols and monosaccharides. The role of Group 1 metal salts in the borate-diol reactions was also investigated by 11B NMR and by the synthesis of model compounds. It was found that the metal cations play an important role in stabilizing the borate-diol complexes in the solid state. In solution, it was found that cross-linking is enhanced by the presence of strongly coordinating cations, as

  9. Ultrasonic sound speed of hydrating calcium sulphate hemihydrate; part 1, the calculation of sound speed of slurries and hardened porous material

    NARCIS (Netherlands)

    de Korte, A.C.J.; Brouwers, Jos

    2011-01-01

    This article focuses on the computation of the sound velocity through slurries and hardened products. The purpose is to use the sound velocity to quantify the composition of the fresh slurry as well as the hardening and hardened - porous - material. Therefore the volumetric models for hydration of

  10. Structure of short-range-ordered iron(III)-precipitates formed by iron(II) oxidation in water containing phosphate, silicate, and calcium

    Science.gov (United States)

    Voegelin, A.; Frommer, J.; Vantelon, D.; Kaegi, R.; Hug, S. J.

    2009-04-01

    The oxidation of Fe(II) in water leads to the formation of Fe(III)-precipitates that strongly affect the fate of nutrients and contaminants in natural and engineered systems. Examples include the cycling of As in rice fields irrigated with As-rich groundwater or the treatment of drinking water for As removal. Knowledge of the types of Fe(III)-precipitates forming in such systems is essential for the quantitative modeling of nutrient and contaminant dynamics and for the optimization of water purification techniques on the basis of a mechanistic understanding of the relevant biogeochemical processes. In this study, we investigated the local coordination of Fe, P, and Ca in Fe(III)-precipitates formed by aeration of synthetic Fe(II)-containing groundwater with variable composition (pH 7, 2-30 mg/L Fe(II), 2-20 mg/L phosphate-P, 2-20 mg/L silicate-Si, 8 mM Na-bicarbonate or 2.5 mM Ca-&1.5 mM Mg-bicarbonate). After 4 hours of oxidation, Fe(III)-precipitates were collected on 0.2 µm nylon filters and dried. The precipitates were analyzed by Fe K-edge EXAFS (XAS beamline, ANKA, Germany) and by P and Ca K-edge XANES spectroscopy (LUCIA beamline, SLS, Switzerland). The Fe K-edge EXAFS spectra indicated that local Fe coordination in the precipitates systematically shifted with water composition. As long as water contained P, mainly short-range-ordered Fe(III)-phosphate formed (with molar P/Fe ~0.5). In the absence of P, Fe(III) precipitated as hydrous ferric oxide at high Si/Fe>0.5, as ferrihydrite at intermediate Si/Fe, and mainly as lepidocrocite at Si/Fepatterns. The P K-edge XANES spectra revealed that phosphate was bound to both Fe as well as Ca (if present). The Ca K-edge XANES spectra showed that the mode of Ca uptake by the Fe(III)-precipitates shifted from mainly adsorption at high Fe/P to coprecipitation at low Fe/P ratio. Despite oversaturation, neither calcite nor hydroxyapatite formed to a significant extent. The results from this study indicated that

  11. Evaluation of mechanical strength and hydrate products evolution of calcium aluminate cement, for endodontic applications; Avaliacao da evolucao da resistencia mecanica e dos produtos de hidratacao de um cimento de aluminato de calcio, visando sua aplicacao em endodontia

    Energy Technology Data Exchange (ETDEWEB)

    Luz, A.P.; Borba, N.Z.; Pandolfelli, V.C., E-mail: anapaula.light@gmail.com, E-mail: vicpando@power.ufscar.br [Universidade Federal de Sao Carlos (UFSCar), SP (Brazil). Departamento de Engenharia de Materiais

    2011-07-01

    Mineral trioxide aggregate (MTA) is the most used retrograde filling cement in the endodontic area. Nevertheless, although its composition is similar to the conventional Portland cement, its high cost, long setting time and low mechanical strength have led to a continuous search for new alternative materials. Considering these aspects, the mechanical strength and crystalline phase evolution of a calcium aluminate cement (CAC), during its hydration process, have been evaluated in this work aiming to apply such material for endodontic treatments. Secar 71 cement samples were prepared and kept in contact with water or SBF (simulated body fluid) during 15 days at 37 deg C. Compressive strength, apparent porosity, X ray diffraction and thermogravimetric tests were carried out for the samples evaluation after 1, 3, 7 and 15 days. The main identified phases were CAH{sub 10}, C{sub 2}AH{sub 8}, C{sub 3}AH{sub 6} and AH{sub 3}. Moreover, when in the presence of SBF, some changes in the amount of the hydrates in the CAC samples were observed, which affected the mechanical behavior of the cement. (author)

  12. A realistic molecular model of cement hydrates.

    Science.gov (United States)

    Pellenq, Roland J-M; Kushima, Akihiro; Shahsavari, Rouzbeh; Van Vliet, Krystyn J; Buehler, Markus J; Yip, Sidney; Ulm, Franz-Josef

    2009-09-22

    Despite decades of studies of calcium-silicate-hydrate (C-S-H), the structurally complex binder phase of concrete, the interplay between chemical composition and density remains essentially unexplored. Together these characteristics of C-S-H define and modulate the physical and mechanical properties of this "liquid stone" gel phase. With the recent determination of the calcium/silicon (C/S = 1.7) ratio and the density of the C-S-H particle (2.6 g/cm(3)) by neutron scattering measurements, there is new urgency to the challenge of explaining these essential properties. Here we propose a molecular model of C-S-H based on a bottom-up atomistic simulation approach that considers only the chemical specificity of the system as the overriding constraint. By allowing for short silica chains distributed as monomers, dimers, and pentamers, this C-S-H archetype of a molecular description of interacting CaO, SiO2, and H2O units provides not only realistic values of the C/S ratio and the density computed by grand canonical Monte Carlo simulation of water adsorption at 300 K. The model, with a chemical composition of (CaO)(1.65)(SiO2)(H2O)(1.75), also predicts other essential structural features and fundamental physical properties amenable to experimental validation, which suggest that the C-S-H gel structure includes both glass-like short-range order and crystalline features of the mineral tobermorite. Additionally, we probe the mechanical stiffness, strength, and hydrolytic shear response of our molecular model, as compared to experimentally measured properties of C-S-H. The latter results illustrate the prospect of treating cement on equal footing with metals and ceramics in the current application of mechanism-based models and multiscale simulations to study inelastic deformation and cracking.

  13. Modified tricalcium silicate cement formulations with added zirconium oxide.

    Science.gov (United States)

    Li, Xin; Yoshihara, Kumiko; De Munck, Jan; Cokic, Stevan; Pongprueksa, Pong; Putzeys, Eveline; Pedano, Mariano; Chen, Zhi; Van Landuyt, Kirsten; Van Meerbeek, Bart

    2017-04-01

    This study aims to investigate the effect of modifying tricalcium silicate (TCS) cements on three key properties by adding ZrO 2 . TCS powders were prepared by adding ZrO 2 at six different concentrations. The powders were mixed with 1 M CaCl 2 solution at a 3:1 weight ratio. Biodentine (contains 5 wt.% ZrO 2 ) served as control. To evaluate the potential effect on mechanical properties, the mini-fracture toughness (mini-FT) was measured. Regarding bioactivity, Ca release was assessed using ICP-AES. The component distribution within the cement matrix was evaluated by Feg-SEM/EPMA. Cytotoxicity was assessed using an XTT assay. Adding ZrO 2 to TCS did not alter the mini-FT (p = 0.52), which remained in range of that of Biodentine (p = 0.31). Ca release from TSC cements was slightly lower than that from Biodentine at 1 day (p > 0.05). After 1 week, Ca release from TCS 30 and TCS 50 increased to a level that was significantly higher than that from Biodentine (p  0.05). EPMA revealed a more even distribution of ZrO 2 within the TCS cements. Particles with an un-reacted core were surrounded by a hydration zone. The 24-, 48-, and 72-h extracts of TCS 50 were the least cytotoxic. ZrO 2 can be added to TCS without affecting the mini-FT; Ca release was reduced initially, to reach a prolonged release thereafter; adding ZrO 2 made TCS cements more biocompatible. TCS 50 is a promising cement formulation to serve as a biocompatible hydraulic calcium silicate cement.

  14. Influência de aditivos dispersantes e acelerador na hidratação de cimento e cimento-matriz Influence of dispersant and accelerator additives on hydration of calcium aluminate cement and cement-matrix

    Directory of Open Access Journals (Sweden)

    I. R. Oliveira

    2006-09-01

    Full Text Available A aplicação de concretos refratários, principalmente na siderurgia, é um processo em constante evolução, que apresenta uma forte dependência dos avanços dos conhecimentos sobre os ligantes hidráulicos. Isso se deve a influência exercida por estes ligantes nas propriedades reológicas e desenvolvimento de resistência mecânica de concretos. O processo de hidratação dos ligantes é sensivelmente influenciado pela presença de aditivos, afetando o tempo requerido para efetuar a desmoldagem do corpo conformado. Além disso, a adição de alumina ao cimento também influencia o seu comportamento de hidratação, bem como a extensão do período de indução, a composição das fases e dos produtos de hidratação. Assim, neste trabalho foi estudada a influência da presença de aditivos dispersantes e/ou acelerador no processo de hidratação de cimento e cimento-matriz. Independente do sistema, os aditivos dispersantes atuaram como retardadores do processo de hidratação, principalmente para o caso do ácido cítrico e citrato de diamônio. Tais aditivos apresentaram-se também como os mais eficientes para a combinação com o acelerador Li2CO3, resultando em um tempo de pega intermediário. Isto mostra ser possível controlar a trabalhabilidade reduzindo o tempo para a desmoldagem.A growing demand for refractory castables with specific behaviors has been promoting a continuous technological evolution, in which, one of the most important aspects concerns in a deep knowledge of hydraulic binders. These materials present a great influence on the rheological properties and mechanical strength development of castables, defining their workability periods and demoulding times, respectively. The hydration process of calcium aluminate cement is influenced by the presence of additives, which affects the setting and demoulding time of the shaped body. Besides that, the alumina addition to cement also influences the hydration behaviour, as well

  15. Gas hydrates

    Digital Repository Service at National Institute of Oceanography (India)

    Ramprasad, T.

    . faulting and fluid migration, and 4. trapping of free gas beneath a hydrate seal. Experiments are being conducted to assess the impact of gas hydrate on sediment behavior, particularly with respect to slope failure and other potential geohazards....K. Paull, R. Matsumoto, P.J. Wallace, and W.P. Dillon (Eds.), Proceedings ODP, Scientific Results, v. 164 College Station, TX (Ocean Drilling Program), pp. 179-191. Dallimore, S. R., T. Uchida, and T. S. Collett, 1999, Summary, in S. R. Dallimore, T...

  16. Hydration Properties of Ground Granulated Blast-Furnace Slag (GGBS Under Different Hydration Environments

    Directory of Open Access Journals (Sweden)

    Shuhua LIU

    2017-02-01

    Full Text Available The hydration properties of various cementitious materials containing Ground Granulated Blast-furnace Slag (GGBS, two alkali-activated slag cements (AAS-1 and AAS-2 in which sodium silicate and sodium hydroxide act as alkaline activators respectively, supersulfated cement (SSC and slag Portland cement(PSC, are compared with ordinary Portland cement (OPC to investigate the effect of activating environment on the hydration properties in this study by determining the compressive strength of the pastes, the hydration heat of binders within 96 hours, and the hydration products at age of 28 days. The results show that C-S-H gels are the main hydrated products for all cementitious systems containing GGBS. Ca(OH2 is the hydration products of OPC and PSC paste. However, ettringite and gypsum crystals instead of Ca(OH2 are detected in SSC paste. Additionally, tobermorite, a crystalline C-S-H, and calcite are hydrated products in AAS-1. Tobermorite, cowlesite and calcite are hydrated products of AAS-2 as well. Based on strength results, AAS-1 paste exhibits the highest compressive strength followed by POC, PSC, SSC in order at all testing ages and AAS-2 give the lowest compressive strength except for the early age at 3 days, which is higher than SSC but still lower than PSC. From hydration heat analysis, alkalinity in the reaction solution is a vital factor influencing the initial hydration rate and the initial hydration rate from higher to lower is AAS-2, AAS-1, OPC, PSC and SSC. Although AAS possesses a faster reaction rate in the initial hours, cumulative hydration heat of AAS is comparably lower than that of OPC, but higher than those of PSC and SSC in turn, which indicates that the hydration heat of clinkers is much higher than that of slag.DOI: http://dx.doi.org/10.5755/j01.ms.23.1.14934

  17. In situ assessment of the setting of tricalcium silicate-based sealers using a dentin pressure model.

    Science.gov (United States)

    Xuereb, Maria; Vella, Paul; Damidot, Denis; Sammut, Charles V; Camilleri, Josette

    2015-01-01

    EndoSequence BC Sealer (Brasseler, Savannah, GA) is a premixed tricalcium silicate-based root canal sealer that requires moisture from the root dentin to hydrate. The aim of this study was to investigate the setting of EndoSequence BC Sealer and other sealers in contact with human dentin in a simulated clinical environment. EndoSequence BC Sealer, MTA Fillapex (Angelus, Londrina, Brazil), Septodont Sealer (Septodont, Saint Maur-des-Fosses, France), and Apexit Plus (Ivoclar, Schaan, Lichtenstein) were assessed. Caries-free lower premolars extracted for orthodontic purposes in patients aged 13-16 years were standardized to a 10-mm root length and were filled with test sealers and set up in a dentin pressure model for 14 days. In addition, set sealers immersed in physiologic solution for 14 days were also assessed. The set materials in solution and materials retrieved from the dentin pressure setup were characterized by scanning electron microscopy and X-ray diffraction analysis. The setting time and radiopacity were assessed using ISO 6876:2002 specifications. Furthermore, mineral ion leaching was evaluated by inductively coupled plasma mass spectrometry. All the sealers tested exhibited formation of a calcium phosphate phase when in contact with physiologic solution. Septodont Sealer and Apexit Plus did not exhibit the formation of a calcium phosphate phase in the dentin pressure setup. The fluid in the system was enough to allow the setting of EndoSequence BC Sealer, which did not set in a dry environment. All materials leached calcium with the Septodont Sealer, exhibiting double the calcium ion leaching compared with EndoSequence BC Sealer. Using the dentinal fluid pressure system resulted in an adequate flow of dentinal fluid that allowed EndoSequence BC Sealer to set inside the root canal. Although the sealers tested were tricalcium silicate based, the hydration reaction and bioactivity in the presence of dentinal fluid were different to hydration in vitro. Thus

  18. Silicate volcanism on Io

    Science.gov (United States)

    Carr, M. H.

    1986-03-01

    This paper is mainly concerned with the nature of volcanic eruptions on Io, taking into account questions regarding the presence of silicates or sulfur as principal component. Attention is given to the generation of silicate magma, the viscous dissipation in the melt zone, thermal anomalies at eruption sites, and Ionian volcanism. According to the information available about Io, it appears that its volcanism and hence its surface materials are dominantly silicic. Several percent of volatile materials such as sulfur, but also including sodium- and potassium-rich materials, may also be present. The volatile materials at the surface are continually vaporized and melted as a result of the high rates of silicate volcanism.

  19. Silicate fertilizer and irrigation depth in corn production

    Directory of Open Access Journals (Sweden)

    Edvaldo Eloy Dantas Júnior

    2013-08-01

    Full Text Available Calcium-magnesium silicates improve the soil physicochemical properties and provide benefits to plant nutrition, since they are sources of silica, calcium and magnesium. The objective of this study was to evaluate the grain yield of irrigated corn fertilized with calcium-magnesium silicate. The experiment was carried out in a greenhouse in Campina Grande - PB, Brazil, using plastic pots containing 80 kg of soil. The treatments consisted of the combination of four irrigation depths, related to water replacement of 50, 75, 100 and 125% of the crop evapotranspiration, with fertilizer levels of 0, 82, 164 and 246 g of calcium-magnesium silicate, with three replications. The experimental design was in randomized blocks, with the irrigation depths distributed in bands while the silicon levels constituted the subplots. Corn yield was influenced by calcium-magnesium silicate and by irrigation depth, obtaining the greatest grain yield with the dose of 164 g pot-1 irrigated at the highest water level. The water-use efficiency of in corn production tended to decrease when the irrigation depth was increased. The best water-use efficiency was observed when the irrigation level was between 87 and 174 mm, and the dose of silicate was 164 g pot-1.

  20. Nanostructured silicate polymer concrete

    Directory of Open Access Journals (Sweden)

    Figovskiy Oleg L'vovich

    2014-03-01

    Full Text Available It has been known that acid-resistant concretes on the liquid glass basis have high porosity (up to 18~20 %, low strength and insufficient water resistance. Significant increasing of silicate matrix strength and density was carried out by incorporation of special liquid organic alkali-soluble silicate additives, which block superficial pores and reduce concrete shrinkage deformation. It was demonstrated that introduction of tetrafurfuryloxisilane additive sharply increases strength, durability and shock resistance of silicate polymer concrete in aggressive media. The experiments showed, that the strength and density of silicate polymer concrete increase in case of decreasing liquid glass content. The authors obtained optimal content of silicate polymer concrete, which possesses increased strength, durability, density and crack-resistance. Diffusive permeability of concrete and its chemical resistance has been investigated in various corroding media.

  1. Suprimento do silicato de cálcio e a eficiência nutricional de variedades de cafeeiro Effect of calcium silicate suplly and the nutritional efficiency of coffee cultivars

    Directory of Open Access Journals (Sweden)

    Adélia Aziz Alexandre Pozza

    2009-12-01

    Full Text Available Embora não seja considerado nutriente essencial às plantas, o Si é classificado como elemento benéfico ou útil, mas pode alterar a dinâmica nutricional das plantas. Objetivando comparar a eficiência nutricional de variedades de cafeeiro (Catuaí, Mundo Novo e Icatu em resposta à adubação silicatada, realizou-se um experimento em blocos casualizados, com as três variedades de mudas em tubetes combinadas com seis doses de CaSiO3 (T0 = 0, T1 = 0,063, T2 = 0,125, T3 = 0,25, T4 = 0,5 e T5 = 1,0 g dm-3 de substrato. A variedade Icatu teve a maior eficiência de absorção (EA de Cu, Zn, Fe e Si, maior eficiência de uso (EU de N, K, Ca, B e Mn, não diferindo da Mundo Novo com relação aos nutrientes N, Ca e Mn, e maior eficiência de translocação (ET de N, S, Zn e de Fe. A Catuaí teve maior EA de P, K, B e Mn, não diferindo da Mundo Novo com relação aos nutrientes P, K e Mn, maior EU para Mg, S, Cu, Zn, Fe e Si, provavelmente devido à melhor ET desses nutrientes, exceto para Fe e Si. A Mundo Novo foi mais eficiente na absorção de N, K, Ca, Mg, Mn e Si, teve maior EU de P e Mn e maior ET de K, Ca, B, Mn e Si.Silicon is classified as a beneficial nutrient and can improve the nutritional dynamics of plants, although it is not considered an essential nutrient for plants. In an experiment in a randomized block design, three coffee cultivars (Catuaí, Mundo Novo and Icatu were planted in plastic tubes, combined with six doses of calcium silicate (T0=0, T1=0.063, T2=0.125, T3=0.25, T4=0.5 and T5=1.0 g dm-3 substrate, to compare the nutritional efficiency of the cultivars in response to silicon fertilization. Cultivar Icatu showed the higher uptake efficiency (UE of Cu, Zn, Fe, and Si, and efficiency of use (EU of N, K, Ca, B, and Mn, but the later did not differ from Mundo Novo cultivar (N, Ca, and Mn. The efficiency of translocation (ET was higher for N, S, Zn, and Fe. For Catuaí the uptake efficiency of P, K, B, and Mn was higher

  2. Natural Gas Hydrates

    OpenAIRE

    Ersland, Geir

    2010-01-01

    The experimental set-up with the MRI monitoring apparatus was capable of forming large quantities of methane hydrates in sandstone pores and monitor hydrate growth patterns for various initial conditions. Spontaneous conversion of methane hydrate to carbon dioxide hydrate occurred when methane hydrate, in porous media, was exposed to liquid carbon dioxide. The MRI images did not detect any significant increase in signal in the hydrate saturated cores that would indicate the presence of free w...

  3. Effects of silicate application on soil fertility and wheat yield

    Directory of Open Access Journals (Sweden)

    Marcos Vinícius Mansano Sarto

    2015-12-01

    Full Text Available An improvement in soil chemical properties and crop development with silicate application has been confirmed in several plant species. The effects of silicate application on soil chemical properties and wheat growth were investigated in the present study. The experiment was carried out in 8-L plastic pots in a greenhouse. Treatments were arranged in a randomized block design in a 3 × 5 factorial: three soils [Rhodic Acrudox (Ox1, Rhodic Hapludox (Ox2 and Arenic Hapludult (Ult] and five silicate rates (0, 1, 2, 4 and 6 Mg ha–1 of calcium/magnesium silicate, with four replications. The plant length, number of spikes per pot, shoot dry matter and grain yield, were measured after 115 days of wheat (Triticum aestivum L. growth. Changes in the soil chemical properties (pH, H+ + Al3+, Al3+, P, K, Ca, Mg, Si, Cu, Zn, Fe and Mn were analyzed after wheat harvest. Application of calcium/magnesium silicate reduces the potential acidity (H+ + Al3+ and Al3+ phytotoxic; and increases the soil pH, available Ca, Mg and Si, cation exchange capacity (CEC and soil base saturation. Silicate application did not affect the available P, exchangeable K and availability of micronutrients (Cu, Zn, Fe and Mn in the three soils. The application of calcium/magnesium silicate in an acid clayey Rhodic Hapludox improves the development and yield of wheat; however, the silicate application in soil with pH higher to 5.3 and high Si availability does not affect the agronomic characteristics and grain yield of wheat. 

  4. Limestone reaction in calcium aluminate cement–calcium sulfate systems

    OpenAIRE

    Bizzozero, Julien; Scrivener, Karen

    2015-01-01

    This paper reports a study of ternary blends composed of calcium aluminate cement, calcium sulfate hemihydrate and limestone. Compressive strength tests and hydration kinetics were studied as a function of limestone and calcium sulfate content. The phase evolution and the total porosity were followed and compared to thermodynamic simulation to understand the reactions involved and the effect of limestone on these binders. The reaction of limestone leads to the formation of hemicarboaluminate ...

  5. Polymer-Layer Silicate Nanocomposites

    DEFF Research Database (Denmark)

    Potarniche, Catalina-Gabriela

    Nowadays, some of the material challenges arise from a performance point of view as well as from recycling and biodegradability. Concerning these aspects, the development of polymer layered silicate nanocomposites can provide possible solutions. This study investigates how to obtain polymer layered...... silicate nanocomposites and their structure-properties relationship. In the first part of the thesis, thermoplastic layered silicates were obtained by extrusion. Different modification methods were tested to observe the intercalation treatment effect on the silicate-modifier interactions. The silicate...

  6. Gypsum hydration: a theoretical and experimental study

    NARCIS (Netherlands)

    Yu, Qingliang; Brouwers, Jos; de Korte, A.C.J.; Fischer, H.B; Bode, K.A.

    2009-01-01

    Calcium sulphate dihydrate (CaSO4·2H2O or gypsum) is used widely as building material because of its excellent fire resistance, aesthetics, and low price. Hemihydrate occurs in two formations of α- and β-type. Among them β-hemihydrate is mainly used to produce gypsum plasterboard since the hydration

  7. Hydration states of AFm cement phases

    Energy Technology Data Exchange (ETDEWEB)

    Baquerizo, Luis G., E-mail: luis.baquerizoibarra@holcim.com [Innovation, Holcim Technology Ltd., CH-5113 Holderbank (Switzerland); Matschei, Thomas [Innovation, Holcim Technology Ltd., CH-5113 Holderbank (Switzerland); Scrivener, Karen L. [Laboratory of Construction Materials, Ecole Polytechnique Fédérale de Lausanne, CH-1015 Lausanne (Switzerland); Saeidpour, Mahsa; Wadsö, Lars [Building Materials, Lund University, Box 124, 221 000 Lund (Sweden)

    2015-07-15

    The AFm phase, one of the main products formed during the hydration of Portland and calcium aluminate cement based systems, belongs to the layered double hydrate (LDH) family having positively charged layers and water plus charge-balancing anions in the interlayer. It is known that these phases present different hydration states (i.e. varying water content) depending on the relative humidity (RH), temperature and anion type, which might be linked to volume changes (swelling and shrinkage). Unfortunately the stability conditions of these phases are insufficiently reported. This paper presents novel experimental results on the different hydration states of the most important AFm phases: monocarboaluminate, hemicarboaluminate, strätlingite, hydroxy-AFm and monosulfoaluminate, and the thermodynamic properties associated with changes in their water content during absorption/desorption. This data opens the possibility to model the response of cementitious systems during drying and wetting and to engineer systems more resistant to harsh external conditions.

  8. The utilization of waste by-products for removing silicate from mineral processing wastewater via chemical precipitation.

    Science.gov (United States)

    Kang, Jianhua; Sun, Wei; Hu, Yuehua; Gao, Zhiyong; Liu, Runqing; Zhang, Qingpeng; Liu, Hang; Meng, Xiangsong

    2017-11-15

    This study investigates an environmentally friendly technology that utilizes waste by-products (waste acid and waste alkali liquids) to treat mineral processing wastewater. Chemical precipitation is used to remove silicate from scheelite (CaWO4) cleaning flotation wastewater and the waste by-products are used as a substitute for calcium chloride (CaCl2). A series of laboratory experiments is conducted to explain the removal of silicate and the characterization and formation mechanism of calcium silicate. The results show that silicate removal reaches 90% when the Ca:Si molar ratio exceeds 1.0. The X-ray diffraction (XRD) results confirm the characterization and formation of calcium silicate. The pH is the key factor for silicate removal, and the formation of polysilicic acid with a reduction of pH can effectively improve the silicate removal and reduce the usage of calcium. The economic analysis shows that the treatment costs with waste acid (0.63 $/m(3)) and waste alkali (1.54 $/m(3)) are lower than that of calcium chloride (2.38 $/m(3)). The efficient removal of silicate is confirmed by industrial testing at a plant. The results show that silicate removal reaches 85% in the recycled water from tailings dam. Copyright © 2017 Elsevier Ltd. All rights reserved.

  9. Statistical Analyses of Optimum Partial Replacement of Cement by Fly Ash Based on Complete Consumption of Calcium Hydroxide

    Directory of Open Access Journals (Sweden)

    Ouypornprasert Winai

    2016-01-01

    Full Text Available The objectives of this technical paper were to propose the optimum partial replacement of cement by fly ash based on the complete consumption of calcium hydroxide from hydration reactions of cement and the long-term strength activity index based on equivalent calcium silicate hydrate as well as the propagation of uncertainty due to randomness inherent in main chemical compositions in cement and fly ash. Firstly the hydration- and pozzolanic reactions as well as stoichiometry were reviewed. Then the optimum partial replacement of cement by fly ash was formulated. After that the propagation of uncertainty due to main chemical compositions in cement and fly ash was discussed and the reliability analyses for applying the suitable replacement were reviewed. Finally an applicability of the concepts mentioned above based on statistical data of materials available was demonstrated. The results from analyses were consistent with the testing results by other researchers. The results of this study provided guidelines of suitable utilization of fly ash for partial replacement of cement. It was interesting to note that these concepts could be extended to optimize partial replacement of cement by other types of pozzolan which were described in the other papers of the authors.

  10. Silicate Urolithiasis during Long-Term Treatment with Zonisamide

    Directory of Open Access Journals (Sweden)

    Satoru Taguchi

    2013-01-01

    Full Text Available Silicate urinary calculi are rare in humans, with an incidence of 0.2% of all urinary calculi. Most cases were related to excess ingestion of silicate, typically by taking magnesium trisilicate as an antacid for peptic ulcers over a long period of time; however, there also existed unrelated cases, whose mechanism of development remains unclear. On the other hand, zonisamide, a newer antiepileptic drug, is one of the important causing agents of iatrogenic urinary stones in patients with epilepsy. The supposed mechanism is that zonisamide induces urine alkalinization and then promotes crystallization of urine components such as calcium phosphate by inhibition of carbonate dehydratase in renal tubular epithelial cells. Here, we report a case of silicate urolithiasis during long-term treatment with zonisamide without magnesium trisilicate intake and discuss the etiology of the disease by examining the silicate concentration in his urine.

  11. Biological and therapeutic effects of ortho-silicic acid and some ortho-silicic acid-releasing compounds: New perspectives for therapy

    Directory of Open Access Journals (Sweden)

    Jurkić Lela Munjas

    2013-01-01

    Full Text Available Abstract Silicon (Si is the most abundant element present in the Earth's crust besides oxygen. However, the exact biological roles of silicon remain unknown. Moreover, the ortho-silicic acid (H4SiO4, as a major form of bioavailable silicon for both humans and animals, has not been given adequate attention so far. Silicon has already been associated with bone mineralization, collagen synthesis, skin, hair and nails health atherosclerosis, Alzheimer disease, immune system enhancement, and with some other disorders or pharmacological effects. Beside the ortho-silicic acid and its stabilized formulations such as choline chloride-stabilized ortho-silicic acid and sodium or potassium silicates (e.g. M2SiO3; M= Na,K, the most important sources that release ortho-silicic acid as a bioavailable form of silicon are: colloidal silicic acid (hydrated silica gel, silica gel (amorphous silicon dioxide, and zeolites. Although all these compounds are characterized by substantial water insolubility, they release small, but significant, equilibrium concentration of ortho-silicic acid (H4SiO4 in contact with water and physiological fluids. Even though certain pharmacological effects of these compounds might be attributed to specific structural characteristics that result in profound adsorption and absorption properties, they all exhibit similar pharmacological profiles readily comparable to ortho-silicic acid effects. The most unusual ortho-silicic acid-releasing agents are certain types of zeolites, a class of aluminosilicates with well described ion(cation-exchange properties. Numerous biological activities of some types of zeolites documented so far might probably be attributable to the ortho-silicic acid-releasing property. In this review, we therefore discuss biological and potential therapeutic effects of ortho-silicic acid and ortho-silicic acid -releasing silicon compounds as its major natural sources.

  12. First investigations on the quaternary system Na2O-K2O-CaO-SiO2: synthesis and crystal structure of the mixed alkali calcium silicate K1.08Na0.92Ca6Si4O15

    Science.gov (United States)

    Kahlenberg, Volker; Mayerl, Michael Jean-Philippe; Schmidmair, Daniela; Krüger, Hannes; Tribus, Martina

    2017-09-01

    In the course of an exploratory study on the quaternary system Na2O-K2O-CaO-SiO2 single crystals of the first anhydrous sodium potassium calcium silicate have been obtained from slow cooling of a melt in the range between 1250 and 1050 °C. Electron probe micro analysis suggested the following idealized molar ratios of the oxides for the novel compound: K2O:Na2O:CaO:SiO2 = 1:1:12:8 (or KNaCa6Si4O15). Single-crystal diffraction measurements on a crystal with chemical composition K1.08Na0.92Ca6Si4O15 resulted in the following basic crystallographic data: monoclinic symmetry, space group P 21/c, a = 8.9618(9) Å, b = 7.3594(6) Å, c = 11.2453(11) Å, β= 107.54(1)°, V = 707.2(1) Å3, Z = 2. Structure solution was performed using direct methods. The final least-squares refinement converged at a residual of R(|F|) = 0.0346 for 1288 independent reflections and 125 parameters. From a structural point of view, K1.08Na0.92Ca6Si4O15 belongs to the group of mixed-anion silicates containing [Si2O7]- and [SiO4]-units in the ratio 1:2. The mono- and divalent cations occupy a total of four crystallographically independent positions located in voids between the tetrahedra. Three of these sites are exclusively occupied by calcium. The fourth site is occupied by 54(1)% K and 46%(1) Na, respectively. Alternatively, the structure can be described as a heteropolyhedral framework based on corner-sharing silicate tetrahedra and [CaO6]-octahedra. The network can build up from kröhnkite-like [Ca(SiO4)2O2]-chains running along [001]. A detailed comparison with other A2B6Si4O15-compounds including topological and group-theoretical aspects is presented.

  13. Effect of calcium and magnesium silicate on the growth of the castor oil plant subjected to salinity levels Efeito de silicato de cálcio e magnésio sobre o crescimento de plantas de mamoneira submetidas a níveis de salinidade

    Directory of Open Access Journals (Sweden)

    José Félix Brito Neto

    2012-12-01

    Full Text Available Salt stress decreases the osmotic potential of soil solution causing water stress, causing toxic effects in the plants resulting in injuries on the metabolism and nutritional disorders, thus compromising the plant growth, resulting in lower production. The calcium silicate and magnesium can perform the same function as limestone, besides providing silicon to plants, may also contribute to the resistance of plants to salt stress. Thus, the objective of this study was to evaluate the effect of calcium and magnesium silicate on the growth of the castor oil plant BRS Energia cultivated under saline conditions. This study evaluated plant height, stem diameter, number of leaves, leaf area, dry weight of shoot and root, and soil chemical characteristics. There was no interaction between factors of salinity level and of silicate level regarding the evaluated variables. There was a direct relationship between salinity levels and plant growth in height and stem diameter. The K concentration in soil were affected by salinity levels. O estresse salino diminui o potencial osmótico da solução do solo causando estresse hídrico, provocando efeitos tóxicos nas plantas que resultam em injúrias no metabolismo e desordens nutricionais, comprometendo assim o crescimento das plantas, resultando em menor produção. O silicato de cálcio e magnésio pode desempenhar a mesma função do calcário, além de fornecer silício para as plantas, podendo ainda, contribuir para a resistência de plantas ao estresse salino. Nesse sentido, objetivou-se com esse trabalho avaliar o efeito do silicato de cálcio e magnésio no crescimento da mamoneira BRS Energia cultivada sob condições salinas. Avaliou-se a altura da planta, diâmetro do caule, número de folhas, área foliar, massa seca da parte aérea e da raiz e as características químicas do solo. Não houve interação entre os fatores níveis de salinidade e silicato sobre as variáveis analisadas. Houve rela

  14. First-principles elasticity of monocarboaluminate hydrates

    KAUST Repository

    Moon, J.

    2014-07-01

    The elasticity of monocarboaluminate hydrates, 3CaO·Al2O3·CaCO3·xH2O (x = 11 or 8), has been investigated by first-principles calculations. Previous experimental study revealed that the fully hydrated monocarboaluminate (x = 11) exhibits exceptionally low compressibility compared to other reported calcium aluminate hydrates. This stiff hydration product can contribute to the strength of concrete made with Portland cements containing calcium carbonates. In this study, full elastic tensors and mechanical properties of the crystal structures with different water contents (x = 11 or 8) are computed by first-principles methods based on density functional theory. The results indicate that the compressibility of monocarboaluminate is highly dependent on the water content in the interlayer region. The structure also becomes more isotropic with the addition of water molecules in this region. Since the monocarboaluminate is a key hydration product of limestone added cement, elasticity of the crystal is important to understand its mechanical impact on concrete. Besides, it is put forth that this theoretical calculation will be useful in predicting the elastic properties of other complex cementitous materials and the influence of ion exchange on compressibility.

  15. Artrodese na coluna cervical utilizando SICAP como substituto de enxerto ósseo Artrodesis en la columna cervical utilizando SICAP como sustituto de injerto óseo Cervical spine fusion utilizing silicated calcium phosphate bone graft substitute (SICAP

    Directory of Open Access Journals (Sweden)

    Juliano Fratezi

    2011-01-01

    Tech EE.UU, Reino Unido es un injerto óseo compuesto de calcio-fosfato con una sustitución de silicato en la estructura química, con una estructura tridimensional que parece hueso natural. MÉTODOS: 19 pacientes fueron sometidos a fusión ósea cervical y analizados retrospectivamente. La evaluación radiográfica y la evaluación clínica fueron realizadas utilizandose el cuestionario Neck Disability Index y la escala análoga del dolor (VAS pre y postoperación. RESULTADOS: El período promedio de seguimiento postoperatorio fue de 14 meses ± 5 meses (7-30 meses. Once pacientes fueron sometidos a fusión vía anterior; 5 pacientes vía posterior y 3 pacientes vía anterior y posterior. La revisión radiográfica mostró 19/19 (100% de fusión ósea, ningún caso presentó subsidencia, rotura o soltura de material de implante o movimiento en los niveles fusionados. Ningún ejemplo de osificación heterotópica o de crecimiento óseo intracanal fue observado. Clínicamente, el promedio de las puntuaciones del Neck Disability disminuyeron 13,3 puntos (promedio preop. de 34,5, postop. de 21,2, mejora de 39%, el promedio de VAS para dolor cervical disminuyó 2 puntos (2,7 preop. para 0,7 postop.; mejora de 74,1%. No fueron observadas complicaciones como infección, osteólisis o edema excesivo de las partes blandas. CONCLUSIÓN: Los resultados preliminares obtenidos en esta serie feuron estimulantes con el uso de SICaP como injerto óseo, con sólida fusión ósea obtenida en todos los casos y sin formación de osificación heterotópica o crecimiento de hueso intracanal. SIcaP demuestra ser un sustituto confiable para el injerto óseo autólogo en la columna cervical.OBJECTIVE: Bone graft substitutes have been developed to obviate the need for autograft from the iliac crest and its resultant complications. SiCaP (Actifuse, ApaTech US, UK is a calcium phosphate bone graft substitute with selective controlled silicate substitution in a patented 3-dimensional structure

  16. THE ALUMINA-SILICATES IN STABILIZATION PROCESSES IN FLUIDIZED-BED ASH

    Directory of Open Access Journals (Sweden)

    IVANA PERNA

    2011-03-01

    Full Text Available Presented study of coal fluidized-bed ash solidification was accompanied with specific studies of alumino-silicates residues in ashes. The specific technology of fluid coal burning and its relatively low temperature combustion combines coal burning and decomposition of calcium carbonate added to the fluid layer in the main endeavor to capture all sulfur oxides. The burning temperature seems be decisive to the behavior of clayed residues and calcium carbonate decomposition in connection for the future solidification of fluidized bed ash. The calcareous substances in combination with alumino-silicate residues form solid bodies where silicates play decisive role of long-term stability and insolubility of obtained solids. The position of aluminum ions in clayed residues of burned coal were studied by MAS-NMR with attention on aluminum ion coordination to oxygen and formation of roentgen amorphous phase of poly-condensed calcium alumina-silicate.

  17. SON68 glass dissolution driven by magnesium silicate precipitation

    Science.gov (United States)

    Fleury, Benjamin; Godon, Nicole; Ayral, André; Gin, Stéphane

    2013-11-01

    layer at the interface with the pristine glass, the gel and the secondary phases. B is not fixed in the gel layer but retention of both B and Li retention is evidenced in one part of the hydrated layer corresponding to a narrow interdiffusion layer [40]. The (H/Li) interdiffusion coefficient decreases by several orders of magnitude when the alteration solution is silica-saturated [41]. This interdiffusion coefficient is a relevant parameter for evaluating the passivation phenomenon. It has also been shown that the nanoporosity of the hydrated glass layer plays an important role [40]. It can be deduced that the precipitation of a silicate secondary phase associated with the consumption of silica strongly affects the hydration rate of the glass and as a consequence its alteration. So the precipitation of secondary phase is a motive force which modifies the physico-chemical properties of the reactive interface situated in the gel or probably in the hydrated glass which has a role of passivation. Currently, the notion of reactive interface and its physico-chemical conditions are under investigations. In our study, solid characterizations are difficult so we use only the general notion of a protective gel. The increased calcium concentrations correspond to congruent dissolution of the gel formed before the addition of magnesium. The Ca/Si molar ratio of the gel was estimated from each experiment based on the data for day 29; in each case the ratio was near 0.1. This hypothesis was not taken into account for the experiment with regular Mg additions because no gel alteration occurred between 45 and 63 days. Glass alteration released boron and silicon in the same proportions as in the glass. No gel formation occurred within the balance period except in the experiment with 100 mg L-1 of Mg at t = 0, for which the cases of 10%, 30% and 50% gel formation (percentage of silicon from glass alteration incorporated in the gel) are indicated as examples. Based on the calcium

  18. 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.

  19. Silicates in Alien Asteroids

    Science.gov (United States)

    2009-01-01

    This plot of data from NASA's Spitzer Space Telescopes shows that asteroid dust around a dead 'white dwarf' star contains silicates a common mineral on Earth. The data were taken primarily by Spitzer's infrared spectrograph, an instrument that breaks light apart into its basic constituents. The yellow dots show averaged data from the spectrograph, while the orange triangles show older data from Spitzer's infrared array camera. The white dwarf is called GD 40.

  20. High calcium fly ash geopolymer stabilized lateritic soil and granulated blast furnace slag blends as a pavement base material.

    Science.gov (United States)

    Phummiphan, Itthikorn; Horpibulsuk, Suksun; Rachan, Runglawan; Arulrajah, Arul; Shen, Shui-Long; Chindaprasirt, Prinya

    2018-01-05

    Granulated Blast Furnace Slag (GBFS) was used as a replacement material in marginal lateritic soil (LS) while class C Fly Ash (FA) was used as a precursor for the geopolymerization process to develop a low-carbon pavement base material at ambient temperature. Unconfined Compression Strength (UCS) tests were performed to investigate the strength development of geopolymer stabilized LS/GBFS blends. Scanning Electron Microscopy and X-ray Diffraction analysis were undertaken to examine the role of the various influencing factors on UCS development. The influencing factors studied included GBFS content, Na2SiO3:NaOH ratio (NS:NH) and curing time. The 7-day soaked UCS of FA geopolymer stabilized LS/GBFS blends at various NS:NH ratios tested was found to satisfy the specifications of the Thailand national road authorities. The GBFS replacement was found to be insignificant for the improvement of the UCS of FA geopolymer stabilized LS/GBFS blends at low NS:NH ratio of 50:50. Microstructural analysis indicated the coexistence of Calcium Silicate Hydrate (CSH) and Sodium Alumino Silicate Hydrate products in FA geopolymer stabilized LS/GBFS blends. This research enables GBFS, which is traditionally considered as a waste material, to be used as a replacement and partially reactive material in FA geopolymer pavement applications. Copyright © 2017 Elsevier B.V. All rights reserved.

  1. Investigation on the effects of combining lime and sodium silicate for ...

    African Journals Online (AJOL)

    Expansive clay is unsuitable subgrade material covering about 40% of the area of Ethiopia. Engineering properties of such problematic soils can be improved by chemical stabilization. This study investigated the effects of combining slightly alkaline liquid sodium silicate with hydrated lime for stabilization of expansive clay.

  2. Thermochemistry of Silicates

    Science.gov (United States)

    Costa, Gustavo; Jacobson, Nathan

    2015-01-01

    The thermodynamic properties of vapor and condensed phases of silicates are crucial in many fields of science. These quantities address fundamental questions on the formation, stability, transformation, and physical properties of silicate minerals and silicate coating compositions. Here the thermodynamic activities of silica and other species in solid solution have been measured by the analysis of the corresponding high temperature vapors using Knudsen Effusion Mass Spectrometry (KEMS). In first set of experiments KEMS has been used to examine the volatility sequence of species (Fe, SiO, Mg, O2 and O) present in the vapor phase during heating of fosterite-rich olivine (Fo93Fa7) up to 2400 C and to measure the Fe, SiO and Mg activities in its solid solution. The data of fosterite-rich olivine are essential for thermochemical equilibrium models to predict the atmospheric and surface composition of hot, rocky exoplanets (Lava Planets). In the second set of experiments the measured thermodynamic activities of the silica in Y2O3-SiO2 and Yb2O3-SiO2 systems are used to assess their reactivity and degradation recession as environmental barrier coatings (EBCs) in combustion environments (e.g. non-moveable parts of gas turbine engine).

  3. Efeito do silicato de cálcio e da autoclavagem na supressividade e na conducividade de dois solos à Rhizoctonia solani Influence of calcium silicate and sterilization on the natural suppressiveness and on the conduciveness of two soils to Rhizoctonia solani

    Directory of Open Access Journals (Sweden)

    Fabrício de Ávila Rodrigues

    1999-08-01

    Full Text Available Objetivou-se verificar o efeito da aplicação de silicato de cálcio e da esterilização na supressividade natural de um Latossolo Vermelho-Escuro (LEa álico textura muito argilosa e na conducividade natural de uma Terra Roxa Estruturada eutrófica (TRe ao fungo Rhizoctonia solani, em condições de casa de vegetação. Utilizou-se o delineamento inteiramente casualizado em esquema fatorial 2 x 3 x 2. Os fatores foram: duas classes de solo (LEa e TRe - 0-20 cm; três tratamentos (esterilização ou não por autoclavagem, aplicação de silicato e testemunha e infestação ou não com R. solani, com três repetições e 16 plântulas de feijoeiro por parcela. A aplicação de silicato foi feita incorporando 0,63 g do produto em 1 kg de cada material de solo, seguido de incubação por 30 dias. Para promover a infestação artificial, foram colocados 800 mg de inóculo em 1 kg de cada material de solo. O silicato de cálcio aumentou os teores de Ca trocável e a soma de bases nos dois solos. Um decréscimo na saturação por Al de 70 para 19% e um aumento na saturação por bases de 9 para 21% alteraram significativamente a supressividade natural do LEa à R. solani. Com relação à TRe, a aplicação de silicato não teve nenhum efeito na sua conducividade, dado ao seu natural caráter eutrófico, o qual já é favorável ao desenvolvimento deste fungo. A esterilização não influiu no desenvolvimento de R. solani, o que sugere que os fatores abióticos foram os responsáveis pela supressividade ou conducividade desses solos.The effect of calcium silicate slag and soil sterilization on the natural suppressiveness of a Typic Acrustox (clay Dark Red Latosol -- LEa and the natural conduciveness of an Oxic Haplustoll (TRe to Rhizoctonia solani were studied under greenhouse conditions. The experimental design was a three-replicate completely randomized one, with 2 x 3 x 2 factorial combination of the following treatments: two soil kinds (LEa and

  4. Characterization of early-age hydration processes in lime-ceramic binders using isothermal calorimetry, X-ray diffraction and scanning electron microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Jerman, Miloš; Tydlitát, Vratislav; Keppert, Martin; Čáchová, Monika; Černý, Robert, E-mail: cernyr@fsv.cvut.cz

    2016-06-10

    Highlights: • Early age hydration processes in lime-ceramic binders are analyzed within a wide range of component ratios. • The applied waste ceramic dust exhibits partial hydraulic properties, ettringite and calcite are formed. • Transition from tobermorite- to jennite-like structures is identified by SEM within the first 48 h. • The highest specific hydration heat after 300 h, 63 J/g, is measured for the binder containing 70% ceramic. • Substantial effect of the heat of wetting is observed, ranging from 10 J/g for lime to 3.9 J/g for ceramic. - Abstract: Early-age hydration processes in a lime-ceramic-water system are analyzed within the whole range of possible lime/ceramic ratios. The isothermal calorimetry shows a substantial effect of the heat of wetting on the total heat evolved, ranging from 10 J/g for lime to 3.9 J/g for ceramic. The highest specific hydration heat of 63 J/g during the analyzed 300-h hydration period exhibits the blended binder containing 70% ceramic and 30% lime which correlates well with the highest compressive and bending strengths of the paste prepared using this blend. Portlandite, ettringite and calcite are the main phases identified by the X-ray diffraction analysis after the hydration of ceramic-rich blends. According to the results of scanning electron microscopy, the initial course of pozzolanic reaction is for this type of binders characterized by the transition from tobermorite-like calcium-silicate-hydrate structures into jennite-like structures within the first 48 h. Blends with the ceramic content lower than 70% show a high portion of portlandite, calcite is present in low amount, and the jennite-like structures are observed after 48 h, following the initial formation of components with a very high Ca content. The favorable properties of the ceramic-rich blended binders can be explained by the partial hydraulic character of the ceramic. With the specific hydration heat of 29 J/g after 300 h and compressive strength

  5. Bonding by Hydroxide-Catalyzed Hydration and Dehydration

    Science.gov (United States)

    Gwo, Dz-Hung

    2008-01-01

    A simple, inexpensive method for bonding solid objects exploits hydroxide-catalyzed hydration and dehydration to form silicate-like networks in thin surface and interfacial layers between the objects. The method can be practiced at room temperature or over a wide range of temperatures. The method was developed especially to enable the formation of precise, reliable bonds between precise optical components. The bonds thus formed exhibit the precision and transparency of bonds formed by the conventional optical-contact method and the strength and reliability of high-temperature frit bonds. The method also lends itself to numerous non-optical applications in which there are requirements for precise bonds and/or requirements for bonds, whether precise or imprecise, that can reliably withstand severe environmental conditions. Categories of such non-optical applications include forming composite materials, coating substrates, forming laminate structures, and preparing objects of defined geometry and composition. The method is applicable to materials that either (1) can form silicate-like networks in the sense that they have silicate-like molecular structures that are extensible into silicate-like networks or (2) can be chemically linked to silicate-like networks by means of hydroxide-catalyzed hydration and dehydration. When hydrated, a material of either type features surface hydroxyl (-OH) groups. In this method, a silicate-like network that bonds two substrates can be formed either by a bonding material alone or by the bonding material together with material from either or both of the substrates. Typically, an aqueous hydroxide bonding solution is dispensed and allowed to flow between the mating surfaces by capillary action. If the surface figures of the substrates do not match precisely, bonding could be improved by including a filling material in the bonding solution. Preferably, the filling material should include at least one ingredient that can be hydrated to

  6. Hydrated mineral stratigraphy of Ius Chasma, Valles Marineris

    Science.gov (United States)

    Roach, L.H.; Mustard, J.F.; Swayze, G.; Milliken, R.E.; Bishop, J.L.; Murchie, S.L.; Lichtenberg, K.

    2010-01-01

    New high-resolution spectral and morphologic imaging of deposits on walls and floor of Ius Chasma extend previous geomorphic mapping, and permit a new interpretation of aqueous processes that occurred during the development of Valles Marineris. We identify hydrated mineralogy based on visible-near infrared (VNIR) absorptions. We map the extents of these units with CRISM spectral data as well as morphologies in CTX and HiRISE imagery. Three cross-sections across Ius Chasma illustrate the interpreted mineral stratigraphy. Multiple episodes formed and transported hydrated minerals within Ius Chasma. Polyhydrated sulfate and kieserite are found within a closed basin at the lowest elevations in the chasma. They may have been precipitates in a closed basin or diagenetically altered after deposition. Fluvial or aeolian processes then deposited layered Fe/Mg smectite and hydrated silicate on the chasma floor, postdating the sulfates. The smectite apparently was weathered out of Noachian-age wallrock and transported to the depositional sites. The overlying hydrated silicate is interpreted to be an acid-leached phyllosilicate transformed from the underlying smectite unit, or a smectite/jarosite mixture. The finely layered smectite and massive hydrated silicate units have an erosional unconformity between them, that marks a change in surface water chemistry. Landslides transported large blocks of wallrock, some altered to contain Fe/Mg smectite, to the chasma floor. After the last episode of normal faulting and subsequent landslides, opal was transported short distances into the chasma from a few m-thick light-toned layer near the top of the wallrock, by sapping channels in Louros Valles. Alternatively, the material was transported into the chasma and then altered to opal. The superposition of different types of hydrated minerals and the different fluvial morphologies of the units containing them indicate sequential, distinct aqueous environments, characterized by alkaline

  7. Carbonate-silicate ratio for soil correction and influence on nutrition, biomass production and quality of palisade grass

    Directory of Open Access Journals (Sweden)

    Renato Ferreira de Souza

    2011-10-01

    Full Text Available Silicates can be used as soil correctives, with the advantage of being a source of silicon, a beneficial element to the grasses. However, high concentrations of silicon in the plant would affect the digestibility of the forage. To evaluate the influence of the substitution of the calcium carbonate by calcium silicate on the nutrition, biomass production and the feed quality of the palisade grass [Urochloa brizantha (C. Hochstetter ex A. Rich. R. Webster], three greenhouse experiments were conducted in completely randomized designs with four replications. Experimental units (pots contained a clayey dystrophic Rhodic Haplustox, a sandy clay loam dystrophic Typic Haplustox and a sandy loam dystrophic Typic Haplustox. Each soil received substitution proportions (0, 25, 50, 75 and 100 % of the carbonate by calcium silicate. The increase in the proportion of calcium silicate elevated the concentrations and accumulations of Si, Ca, Mg, and B, reduced Zn and did not alter P in the shoot of plants. The effects of the treatments on the other nutrients were influenced by the soil type. Inclusion of calcium silicate also increased the relative nutritional value and the digestibility and ingestion of the forage, while the concentration and accumulation of crude protein and the neutral detergent and acid detergent fibers decreased. Biomass production and feed quality of the palisade grass were generally higher with the 50 % calcium silicate treatment.

  8. Carbon Mineralization Using Phosphate and Silicate Ions

    Science.gov (United States)

    Gokturk, H.

    2013-12-01

    Carbon dioxide (CO2) reduction from combustion of fossil fuels has become an urgent concern for the society due to marked increase in weather related natural disasters and other negative consequences of global warming. CO2 is a highly stable molecule which does not readily interact with other neutral molecules. However it is more responsive to ions due to charge versus quadrupole interaction [1-2]. Ions can be created by dissolving a salt in water and then aerosolizing the solution. This approach gives CO2 molecules a chance to interact with the hydrated salt ions over the large surface area of the aerosol. Ion containing aerosols exist in nature, an example being sea spray particles generated by breaking waves. Such particles contain singly and doubly charged salt ions including Na+, Cl-, Mg++ and SO4--. Depending on the proximity of CO2 to the ion, interaction energy can be significantly higher than the thermal energy of the aerosol. For example, an interaction energy of 0.6 eV is obtained with the sulfate (SO4--) ion when CO2 is the nearest neighbor [2]. In this research interaction between CO2 and ions which carry higher charges are investigated. The molecules selected for the study are triply charged phosphate (PO4---) ions and quadruply charged silicate (SiO4----) ions. Examples of salts which contain such molecules are potassium phosphate (K3PO4) and sodium orthosilicate (Na4SiO4). The research has been carried out with first principle quantum mechanical calculations using the Density Functional Theory method with B3LYP functional and Pople type basis sets augmented with polarization and diffuse functions. Atomic models consist of the selected ions surrounded by water and CO2 molecules. Similar to the results obtained with singly and doubly charged ions [1-2], phosphate and silicate ions attract CO2 molecules. Energy of interaction between the ion and CO2 is 1.6 eV for the phosphate ion and 3.3 eV for the silicate ion. Hence one can expect that the selected

  9. Gas hydrate in nature

    Science.gov (United States)

    Ruppel, Carolyn D.

    2018-01-17

    Gas hydrate is a naturally occurring, ice-like substance that forms when water and gas combine under high pressure and at moderate temperatures. Methane is the most common gas present in gas hydrate, although other gases may also be included in hydrate structures, particularly in areas close to conventional oil and gas reservoirs. Gas hydrate is widespread in ocean-bottom sediments at water depths greater than 300–500 meters (m; 984–1,640 feet [ft]) and is also present in areas with permanently frozen ground (permafrost). Several countries are evaluating gas hydrate as a possible energy resource in deepwater or permafrost settings. Gas hydrate is also under investigation to determine how environmental change may affect these deposits.

  10. Calcium - urine

    Science.gov (United States)

    Urinary Ca+2; Kidney stones - calcium in urine; Renal calculi - calcium in your urine; Parathyroid - calcium in urine ... Urine calcium level can help your provider: Decide on the best treatment for the most common type of kidney ...

  11. Determination of reactivity rates of silicate particle-size fractions

    Directory of Open Access Journals (Sweden)

    Angélica Cristina Fernandes Deus

    2014-04-01

    Full Text Available The efficiency of sources used for soil acidity correction depends on reactivity rate (RR and neutralization power (NP, indicated by effective calcium carbonate (ECC. Few studies establish relative efficiency of reactivity (RER for silicate particle-size fractions, therefore, the RER applied for lime are used. This study aimed to evaluate the reactivity of silicate materials affected by particle size throughout incubation periods in comparison to lime, and to calculate the RER for silicate particle-size fractions. Six correction sources were evaluated: three slags from distinct origins, dolomitic and calcitic lime separated into four particle-size fractions (2, 0.84, 0.30 and <0.30-mm sieves, and wollastonite, as an additional treatment. The treatments were applied to three soils with different texture classes. The dose of neutralizing material (calcium and magnesium oxides was applied at equal quantities, and the only variation was the particle-size material. After a 90-day incubation period, the RER was calculated for each particle-size fraction, as well as the RR and ECC of each source. The neutralization of soil acidity of the same particle-size fraction for different sources showed distinct solubility and a distinct reaction between silicates and lime. The RER for slag were higher than the limits established by Brazilian legislation, indicating that the method used for limes should not be used for the slags studied here.

  12. Gas hydrate nucleation

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-12-31

    The overall aim of the project was to gain more knowledge about the kinetics of gas hydrate formation especially the early growth phase. Knowledge of kinetics of gas hydrate formation is important and measurements of gas hydrate particle size and concentration can contribute to improve this knowledge. An experimental setup for carrying out experimental studies of the nucleation and growth of gas hydrates has been constructed and tested. Multi wavelength extinction (MWE) was the experimental technique selected for obtaining particle diameter and concentration. The principle behind MWE is described as well as turbidity spectrum analysis that in an initial stage of the project was considered as an alternative experimental technique. Details of the experimental setup and its operation are outlined. The measuring cell consists of a 1 litre horizontal tube sustaining pressures up to 200 bar. Laser light for particle size determination can be applied through sapphire windows. A description of the various auxiliary equipment and of another gas hydrate cell used in the study are given. A computer program for simulation and analysis of gas hydrate experiments is based on the gas hydrate kinetics model proposed by Skovborg and Rasmussen (1993). Initial measurements showed that knowledge of the refractive index of gas hydrates was important in order to use MWE. An experimental determination of the refractive index of methane and natural gas hydrate is described. The test experiments performed with MWE on collectives of gas hydrate particles and experiments with ethane, methane and natural gas hydrate are discussed. Gas hydrate particles initially seem to grow mainly in size and at latter stages in number. (EG) EFP-94; 41 refs.

  13. Silicate release from glass for pharmaceutical preparations.

    Science.gov (United States)

    Bohrer, Denise; Bortoluzzi, Fabiana; Nascimento, Paulo Cícero; Carvalho, Leandro Machado; Ramirez, Adrian Gustavo

    2008-05-01

    Glass is made of polymeric silica and other minor components, which are necessary for turning the silica into a material more easily moldable and resistant to temperature changes. Glass containers for pharmaceutical usage are classified according to their resistance to a chemical attack, a test carried out in the presence of water and heat. The test is designed to show the released alkalinity, a variable dependent on the amount of sodium oxide, one of the minor components added to the glass mass. In this work, the release of silica from glass by action of constituents from pharmaceutical formulations was investigated. The study included products used in large volumes and usually stored in glass containers. Solutions of amino acids, electrolytes, glucose, oligoelements and others such as heparin and sodium bicarbonate were individually stored in glass containers and heated at 121 degrees C for 30min, as in the water attack test. The test was also carried out only with water, where the pH varied from 2 to 12. The released silicate was measured either by photometry or atomic absorption spectrometry, depending on the nature of the sample. The results showed that silicate is released during the heating cycle even if the contact is with pure water only. The pH exerts a considerable influence on the release, being that the higher the pH, the higher the silica dissolved. An elevated pH, however, is not the only factor responsible for silica dissolution. While in the solutions of NaCl, KCl, Mg Cl2 and ZnSO4 and in most of the amino acids, the concentration of silicate was as high as in pure water (0.1-1.0mg Si/L). In the solutions of sodium acetate, bicarbonate and gluconate, its concentration was much higher, over 30mg Si/L. These results were confirmed by the analysis of commercial products, where in solutions of amino acids the level of silicate ranged from 0.14 to 0.19mg Si/L. On the other hand, calcium gluconate, sodium bicarbonate and potassium phosphate presented

  14. COMPARISON OF SOL-GEL SILICATE COATINGS ON Ti SUBSTRATE

    Directory of Open Access Journals (Sweden)

    DIANA HORKAVCOVÁ

    2012-12-01

    Full Text Available The objective of the submitted work was to prepare and to characterize two types of silicate coatings prepared by the sol-gel method using the dip-coating technique on a titanium substrate. Efforts have been made to use mechanical properties of bio-inert titanium and bioactive properties of a silicate layer enriched with an admixture of compounds identified below. The first group consisted of silicate coatings containing silver, brushite and monetite. The other group of silicate coatings contained calcium nitrate and triethyl phosphate. Mechanically and chemically treated titanium substrates were dipped into sols and dried and fired. Silicate coatings from the first group were also chemically treated in 10 mol.l-1 solution of sodium hydroxide. All coatings were measured to determine their adhesive and bioactive properties and furthermore the antibacterial properties were tested in the case of first group. Surfaces of the coated substrates were investigated after the firing and after the individual tests with optical and electron microscopy and X-ray microdiffraction. A tape test demonstrated excellent adhesive property of all coatings to the substrate, classified with degree 5. A static in vitro test demonstrated bioactivity of nearly all the coatings. The basic silicate coating from the first group and one type of coating from the second group were identified as inert. Antibacterial properties of silicate coatings containing silver showed to be different when tested against Escherichia coli bacteria. A complete inhibition of the growth of bacteria under our experimental conditions was observed for the coating containing silver and monetite and a partial inhibition of the growth of bacteria for coatings containing silver and silver in combination with brushite.

  15. Efeito da aplicação de silicato de cálcio no crescimento, no estado nutricional e na produção de matéria seca de mudas de maracujazeiro Effect of application of calcium silicate on growth, nutritional status and dry matter production of passion fruit seedlings

    Directory of Open Access Journals (Sweden)

    Renato de M. Prado

    2005-06-01

    Full Text Available Objetivou-se, com este trabalho, avaliar os efeitos da aplicação de um resíduo industrial (silicato de cálcio ao substrato de produção das mudas de maracujazeiro, como material corretivo, no desenvolvimento, na produção de matéria seca e no estado nutricional das plantas. O delineamento experimental foi em blocos ao acaso, com cinco tratamentos e quatro repetições. As doses de silicato de cálcio foram aplicadas objetivando-se elevar a percentagem de saturação com bases 25, 50, 75 e 100%, correspondendo a 0,45; 0,90; 1,35 e 1,80 g por vaso, respectivamente, além da testemunha sem aplicação. A unidade experimental foi constituída por vasos com 2 dm³ de substrato de um Latossolo Vermelho distrófico. Após 80 dias da semeadura avaliaram-se: a altura, o número de folhas, o diâmetro do caule e a matéria seca da parte aérea e das raízes e, também, os teores de macro e micronutrientes. O resíduo de silicato de cálcio mostrou-se como corretivo de acidez do solo e como fonte de Ca, embora ineficiente fonte de Mg. O maior crescimento das mudas de maracujazeiro esteve associado à saturação por bases do solo de 58%, à concentração de Ca do solo de 19 mmol c dm-3 e teores de Ca na parte aérea de 12,0 g kg-1.This work was carried out with the objective of evaluating the effect of the addition of industrial residue (calcium silicate to the substrate in the production of the passion fruit seedlings, studying the benefits in the development, the production of dry matter and the nutritional state of the plants. The experimental design adapted was a randomized block with 5 treatments and 4 repetitions. The doses of calcium silicate applied were equivalent to raise in half; one; one and half; and twice the dose to elevate percentage of base saturation = 50%, corresponding to the 0; 0.45; 0.90; 1.35 and 1.80 g per pot, respectively, besides a control without application. The experimental unit was constituted of pots with 2 dm³ of a

  16. Phase transitions in biogenic amorphous calcium carbonate

    Science.gov (United States)

    Gong, Yutao

    Geological calcium carbonate exists in both crystalline phases and amorphous phases. Compared with crystalline calcium carbonate, such as calcite, aragonite and vaterite, the amorphous calcium carbonate (ACC) is unstable. Unlike geological calcium carbonate crystals, crystalline sea urchin spicules (99.9 wt % calcium carbonate and 0.1 wt % proteins) do not present facets. To explain this property, crystal formation via amorphous precursors was proposed in theory. And previous research reported experimental evidence of ACC on the surface of forming sea urchin spicules. By using X-ray absorption near-edge structure (XANES) spectroscopy and photoelectron emission microscopy (PEEM), we studied cross-sections of fresh sea urchin spicules at different stages (36h, 48h and 72h after fertilization) and observed the transition sequence of three mineral phases: hydrated ACC → dehydrated ACC → biogenic calcite. In addition, we unexpectedly found hydrated ACC nanoparticles that are surrounded by biogenic calcite. This observation indicates the dehydration from hydrated ACC to dehydrated ACC is inhibited, resulting in stabilization of hydrated ACC nanoparticles. We thought that the dehydration was inhibited by protein matrix components occluded within the biomineral, and we designed an in vitro assay to test the hypothesis. By utilizing XANES-PEEM, we found that SM50, the most abundant occluded matrix protein in sea urchin spicules, has the function to stabilize hydrated ACC in vitro.

  17. Environmental silicate nano-biocomposites

    CERN Document Server

    Pollet, Eric

    2012-01-01

    Environmental Silicate Nano-Biocomposites focuses on nano-biocomposites, which are obtained by the association of silicates such as bioclays with biopolymers. By highlighting recent developments and findings, green and biodegradable nano-composites from both renewable and biodegradable polymers are explored. This includes coverage of potential markets such as packaging, agricultures, leisure and the fast food industry. The knowledge and experience of more than twenty international experts in diverse fields, from chemical and biochemical engineering to applications, is brought together in four different sections covering: Biodegradable polymers and Silicates, Clay/Polyesters Nano-biocomposites, Clay/Agropolymers Nano-biocomposites, and Applications and biodegradation of Nano-biocomposites. By exploring the relationships between the biopolymer structures, the processes, and the final properties Environmental Silicate Nano-Biocomposites explains how to design nano-materials to develop new, valuable, environmenta...

  18. Combustion of Methane Hydrate

    Science.gov (United States)

    Roshandell, Melika

    A significant methane storehouse is in the form of methane hydrates on the sea floor and in the arctic permafrost. Methane hydrates are ice-like structures composed of water cages housing a guest methane molecule. This caged methane represents a resource of energy and a potential source of strong greenhouse gas. Most research related to methane hydrates has been focused on their formation and dissociation because they can form solid plugs that complicate transport of oil and gas in pipelines. This dissertation explores the direct burning of these methane hydrates where heat from the combustion process dissociates the hydrate into water and methane, and the released methane fuels the methane/air diffusion flame heat source. In contrast to the pipeline applications, very little research has been done on the combustion and burning characteristics of methane hydrates. This is the first dissertation on this subject. In this study, energy release and combustion characteristics of methane hydrates were investigated both theoretically and experimentally. The experimental study involved collaboration with another research group, particularly in the creation of methane hydrate samples. The experiments were difficult because hydrates form at high pressure within a narrow temperature range. The process can be slow and the resulting hydrate can have somewhat variable properties (e.g., extent of clathration, shape, compactness). The experimental study examined broad characteristics of hydrate combustion, including flame appearance, burning time, conditions leading to flame extinguishment, the amount of hydrate water melted versus evaporated, and flame temperature. These properties were observed for samples of different physical size. Hydrate formation is a very slow process with pure water and methane. The addition of small amounts of surfactant increased substantially the hydrate formation rate. The effects of surfactant on burning characteristics were also studied. One finding

  19. Methane Hydrates: Chapter 8

    Science.gov (United States)

    Boswell, Ray; Yamamoto, Koji; Lee, Sung-Rock; Collett, Timothy S.; Kumar, Pushpendra; Dallimore, Scott

    2008-01-01

    Gas hydrate is a solid, naturally occurring substance consisting predominantly of methane gas and water. Recent scientific drilling programs in Japan, Canada, the United States, Korea and India have demonstrated that gas hydrate occurs broadly and in a variety of forms in shallow sediments of the outer continental shelves and in Arctic regions. Field, laboratory and numerical modelling studies conducted to date indicate that gas can be extracted from gas hydrates with existing production technologies, particularly for those deposits in which the gas hydrate exists as pore-filling grains at high saturation in sand-rich reservoirs. A series of regional resource assessments indicate that substantial volumes of gas hydrate likely exist in sand-rich deposits. Recent field programs in Japan, Canada and in the United States have demonstrated the technical viability of methane extraction from gas-hydrate-bearing sand reservoirs and have investigated a range of potential production scenarios. At present, basic reservoir depressurisation shows the greatest promise and can be conducted using primarily standard industry equipment and procedures. Depressurisation is expected to be the foundation of future production systems; additional processes, such as thermal stimulation, mechanical stimulation and chemical injection, will likely also be integrated as dictated by local geological and other conditions. An innovative carbon dioxide and methane swapping technology is also being studied as a method to produce gas from select gas hydrate deposits. In addition, substantial additional volumes of gas hydrate have been found in dense arrays of grain-displacing veins and nodules in fine-grained, clay-dominated sediments; however, to date, no field tests, and very limited numerical modelling, have been conducted with regard to the production potential of such accumulations. Work remains to further refine: (1) the marine resource volumes within potential accumulations that can be

  20. Calcium Carbonate

    Science.gov (United States)

    Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not ... for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve ...

  1. Calcium supplements

    Science.gov (United States)

    ... this page: //medlineplus.gov/ency/article/007477.htm Calcium supplements To use the sharing features on this page, please enable JavaScript. WHO SHOULD TAKE CALCIUM SUPPLEMENTS? Calcium is an important mineral for the ...

  2. Hydration testing of athletes.

    Science.gov (United States)

    Oppliger, Robert A; Bartok, Cynthia

    2002-01-01

    Dehydration not only reduces athletic performance, but also places athletes at risk of health problems and even death. For athletes, monitoring hydration has significant value in maximising performance during training and competition. It also offers medical personnel the opportunity to reduce health risks in situations where athletes engage in intentional weight loss. Simple non-invasive techniques, including weight monitoring and urine tests, can provide useful information. Bioimpedance methods tend to be easy to use and fairly inexpensive, but generally lack the precision and accuracy necessary for hydration monitoring. Blood tests appear to be the most accurate monitoring method, but are impractical because of cost and invasiveness. Although future research is needed to determine which hydration tests are the most accurate, we encourage sports teams to develop and implement hydration monitoring protocols based on the currently available methods. Medical personnel can use this information to maximise their team's athletic performance and minimise heat- and dehydration-related health risks to athletes.

  3. Hydrate morphology: Physical properties of sands with patchy hydrate saturation

    Science.gov (United States)

    Dai, S.; Santamarina, J.C.; Waite, William F.; Kneafsey, T.J.

    2012-01-01

    The physical properties of gas hydrate-bearing sediments depend on the volume fraction and spatial distribution of the hydrate phase. The host sediment grain size and the state of effective stress determine the hydrate morphology in sediments; this information can be used to significantly constrain estimates of the physical properties of hydrate-bearing sediments, including the coarse-grained sands subjected to high effective stress that are of interest as potential energy resources. Reported data and physical analyses suggest hydrate-bearing sands contain a heterogeneous, patchy hydrate distribution, whereby zones with 100% pore-space hydrate saturation are embedded in hydrate-free sand. Accounting for patchy rather than homogeneous hydrate distribution yields more tightly constrained estimates of physical properties in hydrate-bearing sands and captures observed physical-property dependencies on hydrate saturation. For example, numerical modeling results of sands with patchy saturation agree with experimental observation, showing a transition in stiffness starting near the series bound at low hydrate saturations but moving toward the parallel bound at high hydrate saturations. The hydrate-patch size itself impacts the physical properties of hydrate-bearing sediments; for example, at constant hydrate saturation, we find that conductivity (electrical, hydraulic and thermal) increases as the number of hydrate-saturated patches increases. This increase reflects the larger number of conductive flow paths that exist in specimens with many small hydrate-saturated patches in comparison to specimens in which a few large hydrate saturated patches can block flow over a significant cross-section of the specimen.

  4. Effects of calcium leaching on diffusion properties of hardened and altered cement pastes

    Science.gov (United States)

    Kurumisawa, Kiyofumi; Haga, Kazuko; Hayashi, Daisuke; Owada, Hitoshi

    2017-06-01

    It is very important to predict alterations in the concrete used for fabricating disposal containers for radioactive waste. Therefore, it is necessary to understand the alteration of cementitious materials caused by calcium leaching when they are in contact with ground water in the long term. To evaluate the long-term transport characteristics of cementitious materials, the microstructural behavior of these materials should be considered. However, many predictive models of transport characteristics focus on the pore structure, while only few such models consider both, the spatial distribution of calcium silicate hydrate (C-S-H), portlandite, and the pore spaces. This study focused on the spatial distribution of these cement phases. The auto-correlation function of each phase of cementitious materials was calculated from two-dimensional backscattered electron imaging, and the three-dimensional spatial image of the cementitious material was produced using these auto-correlation functions. An attempt was made to estimate the diffusion coefficient of chloride from the three-dimensional spatial image. The estimated diffusion coefficient of the altered sample from the three-dimensional spatial image was found to be comparable to the measured value. This demonstrated that it is possible to predict the diffusion coefficient of the altered cement paste by using the proposed model.

  5. Bilateral urinary calculi after treatment with a silicate-containing milk thickener.

    Science.gov (United States)

    Ulinski, Tim; Sabot, Jean-François; Bourlon, Isabelle; Cochat, Pierre

    2004-04-01

    Nephrocalcinosis and/or urinary calculi are rare in infants. Furosemide treatment during the neonatal period, vitamin D intoxication, hereditary diseases such as hyperoxaluria or distal tubular acidosis are among the most common aetiologies. We report the case of a 6-month-old boy with an extra-hepatic biliary duct atresia treated by the Kasai procedure and a gastro-oesophageal reflux treated with a silicate containing milk thickener (Gelopectose, 5.5% colloidal silicate) since the neonatal period. He did not present any other endogenous risk factor for urinary stone formation (normal urinary calcium/creatinine ratio; normal urinary magnesium excretion). The nephrolithiasis was discovered as the boy presented painful episodes of macroscopic haematuria. Ultrasound examination revealed bilateral nephrocalcinosis and multiple bilateral calculi without infection or urinary obstruction. Infrared spectroscopy revealed silicate as the major component suggesting silicate absorption to be responsible for the described symptoms. After replacement of the silicate-containing agent by a silicate-free milk thickener, the lesions were completely reversible as confirmed by repeated renal ultrasound examinations over a 2-month period. Silicate-containing milk thickeners can be responsible for urinary calculi and/or nephrocalcinosis.

  6. N-Acetylcysteine plus Saline Hydration versus Saline Hydration

    African Journals Online (AJOL)

    ) in patients undergoing coronary angiography pretreated with N-acetylcysteine NAC plus saline hydration or saline hydration alone and to determine the association between various risk factors and RCIN. Methods: Patients were ...

  7. Low-δD hydration rinds in Yellowstone perlites record rapid syneruptive hydration during glacial and interglacial conditions

    Science.gov (United States)

    Bindeman, Ilya N.; Lowenstern, Jacob B.

    2016-01-01

    Hydration of silicic volcanic glass forms perlite, a dusky, porous form of altered glass characterized by abundant “onion-skin” fractures. The timing and temperature of perlite formation are enigmatic and could plausibly occur during eruption, during post-eruptive cooling, or much later at ambient temperatures. To learn more about the origin of natural perlite, and to fingerprint the hydration waters, we investigated perlitic glass from several synglacial and interglacial rhyolitic lavas and tuffs from the Yellowstone volcanic system. Perlitic cores are surrounded by a series of conchoidal cracks that separate 30- to 100-µm-thick slivers, likely formed in response to hydration-induced stress. H2O and D/H profiles confirm that most D/H exchange happens together with rapid H2O addition but some smoother D/H variations may suggest separate minor exchange by deuterium atom interdiffusion following hydration. The hydrated rinds (2–3 wt% H2O) transition rapidly (within 30 µm, or by 1 wt% H2O per 10 µm) to unhydrated glass cores. This is consistent with quenched “hydration fronts” where H2O diffusion coefficients are strongly dependent on H2O concentrations. The chemical, δ18O, and δD systematics of bulk glass records last equilibrium between ~110 and 60 °C without chemical exchange but with some δ18O exchange. Similarly, the δ18O of water extracted from glass by rapid heating suggests that water was added to the glass during cooling at hydration at temperatures as low as 60 °C; prolonged exposure to high temperature of 175°–225° during water addition is less likely as the glass would lose alkalies and should alter to clays within days. A compilation of low-temperature hydration diffusion coefficients suggests ~2 orders of magnitude higher rates of diffusion at 60–110 °C temperatures, compared with values expected from extrapolation of high-temperature (>400 °C) experimental data. The thick hydration rinds in perlites, measuring

  8. Natural Weathering Rates of Silicate Minerals

    Science.gov (United States)

    White, A. F.

    2003-12-01

    Silicates constitute more than 90% of the rocks exposed at Earth's land surface (Garrels and Mackenzie, 1971). Most primary minerals comprising these rocks are thermodynamically unstable at surface pressure/temperature conditions and are therefore susceptible to chemical weathering. Such weathering has long been of interest in the natural sciences. Hartt (1853) correctly attributed chemical weathering to "the efficacy of water containing carbonic acid in promoting the decomposition of igneous rocks." Antecedent to the recent interest in the role of vegetation on chemical weathering, Belt (1874) observed that the most intense weathering of rocks in tropical Nicaragua was confined to forested regions. He attributed this effect to "the percolation through rocks of rain water charged with a little acid from decomposing vegetation." Chamberlin (1899) proposed that the enhanced rates of chemical weathering associated with major mountain building episodes in Earth's history resulted in a drawdown of atmospheric CO2 that led to periods of global cooling. Many of the major characteristics of chemical weathering had been described when Merrill (1906) published the groundbreaking volume Rocks, Rock Weathering, and Soils.The major advances since that time, particularly during the last several decades, have centered on understanding the fundamental chemical, hydrologic, and biologic processes that control weathering and in establishing quantitative weathering rates. This research has been driven by the importance of chemical weathering to a number environmentally and economically important issues. Undoubtedly, the most significant aspect of chemical weathering is the breakdown of rocks to form soils, a process that makes life possible on the surface of the Earth. The availability of many soil macronutrients such as magnesium, calcium, potassium, and PO4 is directly related to the rate at which primary minerals weather. Often such nutrient balances are upset by anthropogenic

  9. HYDRATE CORE DRILLING TESTS

    Energy Technology Data Exchange (ETDEWEB)

    John H. Cohen; Thomas E. Williams; Ali G. Kadaster; Bill V. Liddell

    2002-11-01

    The ''Methane Hydrate Production from Alaskan Permafrost'' project is a three-year endeavor being conducted by Maurer Technology Inc. (MTI), Noble, and Anadarko Petroleum, in partnership with the U.S. DOE National Energy Technology Laboratory (NETL). The project's goal is to build on previous and ongoing R&D in the area of onshore hydrate deposition. The project team plans to design and implement a program to safely and economically drill, core and produce gas from arctic hydrates. The current work scope includes drilling and coring one well on Anadarko leases in FY 2003 during the winter drilling season. A specially built on-site core analysis laboratory will be used to determine some of the physical characteristics of the hydrates and surrounding rock. Prior to going to the field, the project team designed and conducted a controlled series of coring tests for simulating coring of hydrate formations. A variety of equipment and procedures were tested and modified to develop a practical solution for this special application. This Topical Report summarizes these coring tests. A special facility was designed and installed at MTI's Drilling Research Center (DRC) in Houston and used to conduct coring tests. Equipment and procedures were tested by cutting cores from frozen mixtures of sand and water supported by casing and designed to simulate hydrate formations. Tests were conducted with chilled drilling fluids. Tests showed that frozen core can be washed out and reduced in size by the action of the drilling fluid. Washing of the core by the drilling fluid caused a reduction in core diameter, making core recovery very difficult (if not impossible). One successful solution was to drill the last 6 inches of core dry (without fluid circulation). These tests demonstrated that it will be difficult to capture core when drilling in permafrost or hydrates without implementing certain safeguards. Among the coring tests was a simulated hydrate

  10. Battery components employing a silicate binder

    Science.gov (United States)

    Delnick, Frank M [Albuquerque, NM; Reinhardt, Frederick W [Albuquerque, NM; Odinek, Judy G [Rio Rancho, NM

    2011-05-24

    A battery component structure employing inorganic-silicate binders. In some embodiments, casting or coating of components may be performed using aqueous slurries of silicates and electrode materials or separator materials.

  11. Submarine silicic volcanism: Processes and products

    Digital Repository Service at National Institute of Oceanography (India)

    Kalangutkar, N.G.; Iyer, S.D.

    The occurrence of submarine silicic volcanics is rare at the mid-oceanic ridges, abyssal depths, seamounts and fracture zones. Hydrothermal processes are active in submarine silicic environments and are associated with host ores of Cu, Au, Ag, Pb...

  12. Evaluation of Calcium Silicate Cement Bond Strength after Using ...

    African Journals Online (AJOL)

    2018-01-24

    Jan 24, 2018 ... Two‑way ANOVA analysis of variance and post hoc Tukey tests were used for analyses (P= 0.05). Results: The highest push‑out bond strength was observed in the Biodentine ..... Effect of blood contamination on the retention characteristics of two endodontic biomaterials in simulated furcation perforations.

  13. Processing and Properties of Chemically Derived Calcium Silicate Cements

    Science.gov (United States)

    1992-02-27

    alone due to the fineness of the powder and the stiffness of the dough which resulted after shear mixing, characterisitics consistent with the large...cements. The lamination of the polymer in the isostatically pressed cement samples could be the reason for high toughness results. Summary and

  14. Hydrothermal Transformation of the Calcium Aluminum Oxide Hydrates CaAl2O4 . 10H2O and Ca2Al2O. 8H2O to Ca3Al2(OH)12 Investigated by In Situ Synchrotron X-ray Powder Diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Jensen,T.; Christensen, A.; Hanson, J.

    2005-01-01

    The hydrothermal transformation of calcium aluminate hydrates were investigated by in situ synchrotron X-ray powder diffraction in the temperature range 25 to 170 C. This technique allowed the study of the detailed reaction mechanism and identification of intermediate phases. The material CaAl{sub 2}O{sub 4}{center_dot}10H{sub 2}O converted to Ca{sub 3}Al{sub 2}(OH){sub 12} and amorphous aluminum hydroxide. Ca{sub 2}Al{sub 2}O{sub 5}{center_dot}8H{sub 2}O transformed via the intermediate phase Ca{sub 4}Al{sub 2}O{sub 7}{center_dot}13H{sub 2}O to Ca{sub 3}Al{sub 2}(OH){sub 12} and gibbsite, Al(OH){sub 3}. The phase Ca{sub 4}Al{sub 2}O{sub 7}{center_dot}19H{sub 2}O reacted via the same intermediate phase to Ca{sub 3}Al{sub 2}(OH){sub 12} and mainly amorphous aluminum hydroxide. The powder pattern of the intermediate phase is reported.

  15. Application of Isomorphic Ca-Si Rocks for the Synthesis of α-C2S Hydrate

    Directory of Open Access Journals (Sweden)

    Raimundas ŠIAUČIŪNAS

    2014-09-01

    Full Text Available There are approximately 35 million t of carbonate opoka and 21 million t of chalk marl in Lithuania. These materials are suitable for the production of various hydraulic binders. In this work, the influence of burning temperature (700 °C – 950 °C and duration (0.5 h – 2 h on the calcination of isomorphic Ca-Si rocks was investigated. The goal was to prepare a mixture of opoka and chalk marl that would be reactive enough for the hydrothermal synthesis of various calcium silicate hydrates, as this would suggest another potential use of these stocks. It was determined that the largest amount of free CaO (59.09 % is obtained after burning opoka for 2 h at 750 °C and after burning chalk marl for 2 h at 800 °C (84.22 %. The remaining CaO is bound to the structure of poorly crystalline pseudowollastonite, which transforms to wollastonite when the temperature of the thermal treatment is increased. Because the calcination temperature of both materials is similar, they can be burned simultaneously; this would significantly simplify the preparation procedure of these mixtures. The optimal temperature for burning the opoka – chalk marl mixture with a molar ratio of CaO/SiO2 = 2 (62.8 % chalk marl and 37.2 % opoka was determined to be 825 °C for 2 h. In this case, the amount of free CaO is the largest and the crystals of formed wollastonite are poorly crystalline. This blend was treated hydrothermally at 200 °C for 24 h. The dominant product of the synthesis was α-C2S hydrate, which in literature was reported to be the main constituent in the production of new hydraulic binder. DOI: http://dx.doi.org/10.5755/j01.ms.20.3.4426

  16. Amended Silicated for Mercury Control

    Energy Technology Data Exchange (ETDEWEB)

    James Butz; Thomas Broderick; Craig Turchi

    2006-12-31

    Amended Silicates{trademark}, a powdered, noncarbon mercury-control sorbent, was tested at Duke Energy's Miami Fort Station, Unit 6 during the first quarter of 2006. Unit 6 is a 175-MW boiler with a cold-side electrostatic precipitator (ESP). The plant burns run-of-the-river eastern bituminous coal with typical ash contents ranging from 8-15% and sulfur contents from 1.6-2.6% on an as-received basis. The performance of the Amended Silicates sorbent was compared with that for powdered activated carbon (PAC). The trial began with a period of baseline monitoring during which no sorbent was injected. Sampling during this and subsequent periods indicated mercury capture by the native fly ash was less than 10%. After the baseline period, Amended Silicates sorbent was injected at several different ratios, followed by a 30-day trial at a fixed injection ratio of 5-6 lb/MMACF. After this period, PAC was injected to provide a comparison. Approximately 40% mercury control was achieved for both the Amended Silicates sorbent and PAC at injection ratios of 5-6 lbs/MMACF. Higher injection ratios did not achieve significantly increased removal. Similar removal efficiencies have been reported for PAC injection trials at other plants with cold-side ESPs, most notably for plants using medium to high sulfur coal. Sorbent injection did not detrimentally impact plant operations and testing confirmed that the use of Amended Silicates sorbent does not degrade fly ash quality (unlike PAC). The cost for mercury control using either PAC or Amended Silicates sorbent was estimated to be equivalent if fly ash sales are not a consideration. However, if the plant did sell fly ash, the effective cost for mercury control could more than double if those sales were no longer possible, due to lost by-product sales and additional cost for waste disposal. Accordingly, the use of Amended Silicates sorbent could reduce the overall cost of mercury control by 50% or more versus PAC for locations where

  17. STUDY OF THE KINETICS OF HYDRATION STRUCTURING AND THE PROPERTIES OF LIME-BELITIC BINDERS BASED OF MARL

    Directory of Open Access Journals (Sweden)

    Zhukov Aleksey Dmitrievich

    2016-04-01

    Full Text Available Lime-belite binder is obtained by low-temperature firing of natural marl, marling or sanding limestone and artificial lime-silica mixtures. The binder with calcium oxide also contains significant amounts of dicalcium silicate and some others materials, the composition and quantity of which depend on the chemical composition and firing temperature of the raw materials used. The authors investigated the kinetics of hydration structures and physicochemical properties of lime-based binders on the basis of belitic marl from Akburly and Porlytau. The formation of resistance is associated not only with the formation of the system of different types of structures - coagulation and crystallization, with the transition of the first to the second, but also with the different stages of formation of crystal structures. The possibility of using lime-belitic binders for the preparation of high-strength products of autoclave hardening is proved. The autoclaved binders used in the manufacture of sand-lime products are prepared with the use of mixtures consisting of 60...70 % lime-belite binder and 30...40 % ground quartz sand.

  18. Aluminum Sulfate 18 Hydrate

    Science.gov (United States)

    Young, Jay A.

    2004-01-01

    A chemical laboratory information profile (CLIP) of the chemical, aluminum sulfate 18 hydrate, is presented. The profile lists physical and harmful properties, exposure limits, reactivity risks, and symptoms of major exposure for the benefit of teachers and students using the chemical in the laboratory.

  19. Microbeam recoil detection for hydration of minerals studies

    Energy Technology Data Exchange (ETDEWEB)

    Sie, S.H.; Suter, G.F. [CSIRO, North Ryde, NSW (Australia). Exploration and Mining Div.; Chekhmir, A.; Green, T.H. [Macquarie Univ., North Ryde, NSW (Australia)

    1993-12-31

    The glancing angle geometry is chosen to enable application of the elastic recoil detection microanalysis on thick geological samples, for hydrogen content determination. Simultaneous PIXE measurements can be used to eliminate the problem of uncertainties in beam charge collection. The method is applied to determine the hydration characteristics of silicates, produced experimentally at high pressure and temperature simulating the lower crust and upper mantle conditions. Preliminary results show that the technique can be applied readily on a microscopic (<100 {mu}m) scale for determination of H at fraction of atomic percent level. 9 refs., 3 figs.

  20. Preparation and in vivo evaluation of a silicate-based composite bone cement.

    Science.gov (United States)

    Ma, Bing; Huan, Zhiguang; Xu, Chen; Ma, Nan; Zhu, Haibo; Zhong, Jipin; Chang, Jiang

    2017-08-01

    Silicate-based cements have been developed as a class of bioactive and biodegradable bone cements owing to their good in vitro bioactivity and ability to dissolve in a simulated body fluid. Until recently, however, the in vivo evidence of their ability to support bone regeneration is still scarce. In the present study, a pilot in vivo evaluation of a silicate-based composite bone cement (CSC) was carried out in a rabbit femur defect model. The cement was composed of tricalcium silicate, 45S5 bioglass and calcium sulfate, and the self-setting properties of the material were established. The in vivo bone integration and biodegradability of CSC were investigated and compared with those of bioactive glass particulates, and a calcium phosphate cement. The results showed that CSC underwent a relatively slower in vivo degradation as compared with bioactive glass and calcium phosphate cement. Histological observation demonstrated that bone contact area at the interface between the surrounding bone and CSC gradually increased with time proceeding. CSC kept its structural integrity during implantation in vivo because of its acceptable mechanical strength. These results provide evidence of effectiveness in vivo and suggest potential clinical applications of the silicate-based composite bone cements.

  1. Thermogravimetric study on the hydration of reactive magnesia and silica mixture at room temperature

    Energy Technology Data Exchange (ETDEWEB)

    Jin, Fei, E-mail: fj232@cam.ac.uk; Al-Tabbaa, Abir

    2013-08-20

    Highlights: • The characteristics of reactive MgO vary significantly in terms of their impurity content and reactivity depending on their sources and calcination conditions. • The synthesis of magnesium silicate hydrate (MSH) is affected by the characteristics of the precursors, i.e., MgO and silica. • The reaction process in the MgO–SiO{sub 2}–H{sub 2}O system can be followed by TGA, and is essential to develop MSH-based materials. - Abstract: The synthesis of magnesium silicate hydrate (MSH), which has wide applications in both construction and environmental fields, has been studied for decades. However, it is known that the characteristics of magnesia (MgO) vary significantly depending on their calcination conditions, which is expected to affect their performance in the MgO–SiO{sub 2}–H{sub 2}O system. This paper investigated the effect of different MgO and silica sources on the formation of magnesium silicate hydrate (MSH) at room temperature. The hydration process was studied by mixing commercial reactive MgO and silica powders with water and curing for 1, 7 and 28 days. The hydration products were analysed with the help of X-ray diffraction (XRD) and thermogravimatric analysis (TGA). The results showed the continuous consumption of MgO and the existence of MSH and brucite and other minor phases such as magnesite and calcite. It is found that the Mg and Si sources have significant effect on the hydration process of MgO–SiO{sub 2}–H{sub 2}O system. The reaction degree is controlled by the availability of dissolved Mg and Si in the solution. The former is determined by the reactivity of MgO and the latter is related to the reactivity of the silica as well as the pH of the system.

  2. Low-δD hydration rinds in Yellowstone perlites record rapid syneruptive hydration during glacial and interglacial conditions

    Science.gov (United States)

    Bindeman, Ilya N.; Lowenstern, Jacob B.

    2016-11-01

    Hydration of silicic volcanic glass forms perlite, a dusky, porous form of altered glass characterized by abundant "onion-skin" fractures. The timing and temperature of perlite formation are enigmatic and could plausibly occur during eruption, during post-eruptive cooling, or much later at ambient temperatures. To learn more about the origin of natural perlite, and to fingerprint the hydration waters, we investigated perlitic glass from several synglacial and interglacial rhyolitic lavas and tuffs from the Yellowstone volcanic system. Perlitic cores are surrounded by a series of conchoidal cracks that separate 30- to 100-µm-thick slivers, likely formed in response to hydration-induced stress. H2O and D/H profiles confirm that most D/H exchange happens together with rapid H2O addition but some smoother D/H variations may suggest separate minor exchange by deuterium atom interdiffusion following hydration. The hydrated rinds (2-3 wt% H2O) transition rapidly (within 30 µm, or by 1 wt% H2O per 10 µm) to unhydrated glass cores. This is consistent with quenched "hydration fronts" where H2O diffusion coefficients are strongly dependent on H2O concentrations. The chemical, δ18O, and δD systematics of bulk glass records last equilibrium between 110 and 60 °C without chemical exchange but with some δ18O exchange. Similarly, the δ18O of water extracted from glass by rapid heating suggests that water was added to the glass during cooling at 400 °C) experimental data. The thick hydration rinds in perlites, measuring hundreds of microns, preserve the original D/H values of hydrating water as a recorder of paleoclimate conditions. Measured δD values in perlitic lavas are -150 to -191 or 20-40 ‰ lower than glass hydrated by modern Yellowstone waters. This suggests that Yellowstone perlites record the low-δD signature of glacial ice. Cooling calculations, combined with the observed high water diffusion coefficients noted for 60-150 °C, suggest that if sufficient hot

  3. In vitro bioactivity of a tricalcium silicate cement

    Energy Technology Data Exchange (ETDEWEB)

    Morejon-Alonso, L.; Bareiro, O.; Santos, L.A. dos, E-mail: loreley.morejon@ufrgs.b [Universidade Federal do Rio Grande do Sul (UFRG), Porto Alegre, RS (Brazil). Escola de Engenharia. Dep. de Materiais; Carrodeguas R, Garcia [Consejo Superior de Investigaciones Cientificas (CSIC), Madrid (Spain). Inst. de Ceramica y Vidrio. Dept. de Ceramica

    2009-07-01

    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 Ca{sub 3}SiO{sub 5}, obtained by sol-gel process, and a Na{sub 2}HPO{sub 4} 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 Ca{sub 3}SiO{sub 5} would be an effective additive to improve the bioactivity and long term strength of conventional CPC. (author)

  4. Overview: Nucleation of clathrate hydrates

    Science.gov (United States)

    Warrier, Pramod; Khan, M. Naveed; Srivastava, Vishal; Maupin, C. Mark; Koh, Carolyn A.

    2016-12-01

    Molecular level knowledge of nucleation and growth of clathrate hydrates is of importance for advancing fundamental understanding on the nature of water and hydrophobic hydrate formers, and their interactions that result in the formation of ice-like solids at temperatures higher than the ice-point. The stochastic nature and the inability to probe the small length and time scales associated with the nucleation process make it very difficult to experimentally determine the molecular level changes that lead to the nucleation event. Conversely, for this reason, there have been increasing efforts to obtain this information using molecular simulations. Accurate knowledge of how and when hydrate structures nucleate will be tremendously beneficial for the development of sustainable hydrate management strategies in oil and gas flowlines, as well as for their application in energy storage and recovery, gas separation, carbon sequestration, seawater desalination, and refrigeration. This article reviews various aspects of hydrate nucleation. First, properties of supercooled water and ice nucleation are reviewed briefly due to their apparent similarity to hydrates. Hydrate nucleation is then reviewed starting from macroscopic observations as obtained from experiments in laboratories and operations in industries, followed by various hydrate nucleation hypotheses and hydrate nucleation driving force calculations based on the classical nucleation theory. Finally, molecular simulations on hydrate nucleation are discussed in detail followed by potential future research directions.

  5. Methane Clathrate Hydrate Prospecting

    Science.gov (United States)

    Duxbury, N.; Romanovsky, V.

    2003-01-01

    A method of prospecting for methane has been devised. The impetus for this method lies in the abundance of CH4 and the growing shortages of other fuels. The method is intended especially to enable identification of subpermafrost locations where significant amounts of methane are trapped in the form of methane gas hydrate (CH4(raised dot)6H2O). It has been estimated by the U.S. Geological Survey that the total CH4 resource in CH4(raised dot) 6H2O exceeds the energy content of all other fossil fuels (oil, coal, and natural gas from non-hydrate sources). Also, CH4(raised dot)6H2O is among the cleanest-burning fuels, and CH4 is the most efficient fuel because the carbon in CH4 is in its most reduced state. The method involves looking for a proxy for methane gas hydrate, by means of the combination of a thermal-analysis submethod and a field submethod that does not involve drilling. The absence of drilling makes this method easier and less expensive, in comparison with prior methods of prospecting for oil and natural gas. The proposed method would include thermoprospecting in combination with one more of the other non-drilling measurement techniques, which could include magneto-telluric sounding and/or a subsurface-electrical-resistivity technique. The method would exploit the fact that the electrical conductivity in the underlying thawed region is greater than that in the overlying permafrost.

  6. Rapid gas hydrate formation process

    Science.gov (United States)

    Brown, Thomas D.; Taylor, Charles E.; Unione, Alfred J.

    2013-01-15

    The disclosure provides a method and apparatus for forming gas hydrates from a two-phase mixture of water and a hydrate forming gas. The two-phase mixture is created in a mixing zone which may be wholly included within the body of a spray nozzle. The two-phase mixture is subsequently sprayed into a reaction zone, where the reaction zone is under pressure and temperature conditions suitable for formation of the gas hydrate. The reaction zone pressure is less than the mixing zone pressure so that expansion of the hydrate-forming gas in the mixture provides a degree of cooling by the Joule-Thompson effect and provides more intimate mixing between the water and the hydrate-forming gas. The result of the process is the formation of gas hydrates continuously and with a greatly reduced induction time. An apparatus for conduct of the method is further provided.

  7. Electrophoretic deposition of magnesium silicates on titanium implants: Ion migration and silicide interfaces

    Energy Technology Data Exchange (ETDEWEB)

    Afshar-Mohajer, M. [Center for Advanced Manufacturing and Material Processing, Department of Mechanical Engineering, Faculty of Engineering, University of Malaya, Kuala Lumpur 50603 (Malaysia); Yaghoubi, A., E-mail: yaghoubi@siswa.um.edu.my [Center for High Impact Research, University of Malaya, Kuala Lumpur 50603 (Malaysia); Ramesh, S., E-mail: ramesh79@um.edu.my [Center for Advanced Manufacturing and Material Processing, Department of Mechanical Engineering, Faculty of Engineering, University of Malaya, Kuala Lumpur 50603 (Malaysia); Bushroa, A.R.; Chin, K.M.C.; Tin, C.C. [Center for Advanced Manufacturing and Material Processing, Department of Mechanical Engineering, Faculty of Engineering, University of Malaya, Kuala Lumpur 50603 (Malaysia); Chiu, W.S. [Low Dimensional Materials Research Center, Department of Physics, University of Malaya, Kuala Lumpur 50603 (Malaysia)

    2014-07-01

    Magnesium silicates (Mg{sub x}SiO{sub y}) and in particular forsterite (Mg{sub 2}SiO{sub 4}) owing to their low thermal expansion mismatch with metals are promising materials for bioactive coating of implants. Here, we report the electrophoretic deposition (EPD) of forsterite onto titanium substrates using different precursors. Unlike bulk samples which achieve full stoichiometry only beyond 1400 °C, non-stoichiometric magnesium silicate rapidly decomposes into magnesium oxide nanowires during sintering. Elemental mapping and X-ray diffraction suggest that oxygen diffusion followed by ion exchange near the substrate leads to formation of an interfacial Ti{sub 5}Si{sub 3} layer. Pre-annealed forsterite powder on the other hand shows a comparatively lower diffusion rate. Overall, magnesium silicate coatings do not exhibit thermally induced microcracks upon sintering as opposed to calcium phosphate bioceramics which are currently in use.

  8. Tailoring polymer properties with layered silicates

    Science.gov (United States)

    Xu, Liang

    Polymer layered silicate nanocomposites have found widespread applications in areas such as plastics, oil and gas production, biomedical, automotive and information storage, but their successful commercialization critically depends on consistent control over issues such as complete dispersion of layered silicate into the host polymer and optimal interaction between the layered silicates and the polymers. Polypropylene is a commercially important polymer but usually forms intercalated structures with organically modified layered silicate upon mixing, even it is pre-treated with compatibilizing agent such as maleic anhydride. In this work, layered silicate is well dispersed in ammonium modified polypropylene but does not provide sufficient reinforcement to the host polymer due to poor interactions. On the other hand, interactions between maleic anhydride modified polypropylene and layered silicate are fine tuned by using a small amount of maleic anhydride and mechanical strength of the resultant nanocomposites are significantly enhanced. In particular, the melt rheological properties of layered silicate nanocomposites with maleic anhydride functionalized polypropylene are contrasted to those based on ammonium-terminated polypropylene. While the maleic anhydride treated polypropylene based nanocomposites exhibit solid-like linear dynamic behavior, consistent with the formation of a long-lived percolated nanoparticle network, the single-end ammonium functionalized polypropylene based nanocomposites demonstrated liquid-like behavior at comparable montmorillonite concentrations. The differences in the linear viscoelasticity are attributed to the presence of bridging interaction in maleic anhydride functionalized nanocomposites, which facilitates formation of a long-lived silicate network mediated by physisorbed polymer chains. Further, the transient shear stress of the maleic anhydride functionalized nanocomposites in start-up of steady shear is a function of the shear

  9. Nanoscale zinc silicate from phytoliths

    Science.gov (United States)

    Qadri, S. B.; Gorzkowski, E. P.; Rath, B. B.; Feng, C. R.; Amarasinghe, R.; Freitas, J. A.; Culbertson, J. C.; Wollmershauser, J. A.

    2017-10-01

    We report a faster, less expensive method of producing zinc silicate nanoparticles. Such particles are used in high volume to make phosphors and anti-corrosion coatings. The approach makes use of phytoliths (plant rocks), which are microscopic, amorphous, and largely silicate particles embedded in plants, that lend themselves to being easily broken down into nanoparticles. Nanoparticles of Zn2SiO4 were produced in a two stage process. In the refinement stage, plant residue, mixed with an appropriate amount of ZnO, was heated in an argon atmosphere to a temperature exceeding 1400 °C for four to six hours and then heated in air at 650 °C to remove excess carbon. TEM shows 50-100 nm nanoparticles. Raman scattering indicates that only the -Zn2SiO4 crystalline phase was present. X-ray analysis indicated pure rhombohedral R 3 bar phase results from using rice/wheat husks. Both samples luminesced predominantly at 523 nm when illuminated with X-rays or UV laser light.

  10. Ductile flow of methane hydrate

    Science.gov (United States)

    Durham, W.B.; Stern, L.A.; Kirby, S.H.

    2003-01-01

    Compressional creep tests (i.e., constant applied stress) conducted on pure, polycrystalline methane hydrate over the temperature range 260-287 K and confining pressures of 50-100 MPa show this material to be extraordinarily strong compared to other icy compounds. The contrast with hexagonal water ice, sometimes used as a proxy for gas hydrate properties, is impressive: over the thermal range where both are solid, methane hydrate is as much as 40 times stronger than ice at a given strain rate. The specific mechanical response of naturally occurring methane hydrate in sediments to environmental changes is expected to be dependent on the distribution of the hydrate phase within the formation - whether arranged structurally between and (or) cementing sediments grains versus passively in pore space within a sediment framework. If hydrate is in the former mode, the very high strength of methane hydrate implies a significantly greater strain-energy release upon decomposition and subsequent failure of hydrate-cemented formations than previously expected.

  11. Gas Hydrate Petroleum System Analysis

    Science.gov (United States)

    Collett, T. S.

    2012-12-01

    In a gas hydrate petroleum system, the individual factors that contribute to the formation of gas hydrate accumulations, such as (1) gas hydrate pressure-temperature stability conditions, (2) gas source, (3) gas migration, and (4) the growth of the gas hydrate in suitable host sediment can identified and quantified. The study of know and inferred gas hydrate accumulations reveal the occurrence of concentrated gas hydrate is mostly controlled by the presence of fractures and/or coarser grained sediments. Field studies have concluded that hydrate grows preferentially in coarse-grained sediments because lower capillary pressures in these sediments permit the migration of gas and nucleation of hydrate. Due to the relatively distal nature of the deep marine geologic settings, the overall abundance of sand within the shallow geologic section is usually low. However, drilling projects in the offshore of Japan, Korea, and in the Gulf of Mexico has revealed the occurrence of significant hydrate-bearing sand reservoirs. The 1999/2000 Japan Nankai Trough drilling confirmed occurrence of hydrate-bearing sand-rich intervals (interpreted as turbidite fan deposits). Gas hydrate was determined to fill the pore spaces in these deposits, reaching saturations up to 80% in some layers. A multi-well drilling program titled "METI Toaki-oki to Kumano-nada" also identified sand-rich reservoirs with pore-filling hydrate. The recovered hydrate-bearing sand layers were described as very-fine- to fine-grained turbidite sand layers measuring from several centimeters up to a meter thick. However, the gross thickness of the hydrate-bearing sand layers were up to 50 m. In 2010, the Republic of Korea conducted the Second Ulleung Basin Gas Hydrate (UBGH2) Drilling Expedition. Seismic data clearly showed the development of a thick, potential basin wide, sedimentary sections characterized by mostly debris flows. The downhole LWD logs and core data from Site UBGH2-5 reveal that each debris flows is

  12. Diurnally-Varying Lunar Hydration

    Science.gov (United States)

    Hendrix, A. R.; Hurley, D.; Retherford, K. D.; Mandt, K.; Greathouse, T. K.; Farrell, W. M.; Vilas, F.

    2016-12-01

    Dayside, non-polar lunar hydration signatures have been observed by a handful of instruments and present insights into the lunar water cycle. In this study, we utilize the unique measurements from the current Lunar Reconnaissance Orbiter (LRO) mission to study the phenomenon of diurnally-varying dayside lunar hydration. The Lyman Alpha Mapping Project (LAMP) onboard LRO senses a strong far-ultraviolet water absorption edge indicating hydration in small abundances in the permanently shadowed regions as well as on the lunar dayside. We report on diurnal variability in hydration in different terrain types. We investigate the importance of different sources of hydration, including solar wind bombardment and meteoroid bombardment, by observing trends during magnetotail and meteor stream crossings.

  13. Effet de différents sels de calcium in vitro et in vivo sur le ...

    African Journals Online (AJOL)

    Objectives: the in vitro and in vivo efficacy of silicate, hydroxide, oxide, sulfate and calcium hypochlorite were tested on the development of fungi responsible for storage rot in melon fruit. Methodology and results : Calcium salts were tested in vitro at 200, 400, 600, 800 and 1000 ppm and in vivo at 600 ppm against Alternaria ...

  14. Silicates materials of high vacuum technology

    CERN Document Server

    Espe, Werner

    2013-01-01

    Materials of High Vacuum Technology, Volume 2: Silicates covers silicate insulators of special importance to vacuum technology. The book discusses the manufacture, composition, and physical and chemical properties of technical glasses, quartz glass, quartzware, vycor glass, ceramic materials, mica, and asbestos.

  15. Flow assurance intervention, hydrates remediation

    Energy Technology Data Exchange (ETDEWEB)

    Mancini, Christopher S. [Oceaneering International Inc., Houston, TX (United States)

    2012-07-01

    This paper addresses the issues of removing hydrates in sub sea flow lines and associated equipment with an Remotely Operated Vehicle (ROV) of opportunity and a multi-service-vessel (MSV). The paper is split into three topics: the equipment used with the ROV, assessing the interface points and handling fluids produced from drawing down the pressure. Each section is explained thoroughly and backed up with real world experience. The equipment section details information from actual jobs performed and why the particular components were utilized. The system is generally contained in an ROV mounted skid. Pumps are utilized to draw down the pressure inside the hydrated section of equipment, removing one of the three necessary components for hydrates formation. Once the section is pumped down, several options exist for handling the fluids pumped out of the system: pumping to surface, re-injection into the well, or injection into an operating flow line. This method of hydrates remediation is both economical and timely. Hydrate blockages form in low temperatures and high pressures. Reducing the pressure or increasing the temperature so the conditions lie to the right of the hydrate dissociation curve will slowly decompose the blockage. Depressurization and the use of MEG or methanol will give favorable conditions to remove the hydrate plug. Oceaneering has the capabilities to remove hydrates using the FRS in conjunction with an installation vessel to dispose of the gas and fluid removed from the flow line. Hydrate remediation techniques should be implemented into the initial design to reduce costs later. The cost of stopped production combined with the day rate for equipment needed for hydrate removal outweighs the costs if no technique is utilized. (author)

  16. Shifting Focus: From Hydration for Performance to Hydration for Health.

    Science.gov (United States)

    Perrier, Erica T

    2017-01-01

    Over the past 10 years, literature on hydration biomarkers has evolved considerably - from (de)hydration assessment towards a more global definition of biomarkers of hydration in daily life. This shift in thinking about hydration markers was largely driven by investigating the differences that existed between otherwise healthy individuals whose habitual, ad-libitum drinking habits differ, and by identifying physiological changes in low-volume drinkers who subsequently increase their water intake. Aside from obvious differences in urinary volume and concentration, a growing body of evidence is emerging that links differences in fluid intake with small, but biologically significant, differences in vasopressin (copeptin), glomerular filtration rate, and markers of metabolic dysfunction or disease. Taken together, these pieces of the puzzle begin to form a picture of how much water intake should be considered adequate for health, and represent a shifting focus from hydration for performance, toward hydration for health outcomes. This narrative review outlines the key areas of research in which the global hydration process - including water intake, urinary hydration markers, and vasopressin - has been associated with health outcomes, focusing on kidney and metabolic endpoints. It will also provide a commentary on how various hydration biomarkers may be used in hydration for health assessment. Finally, if adequate water intake can play a role in maintaining health, how might we tell if we are drinking enough? Urine output is easily measured, and can take into account differences in daily physical activity, climate, dietary solute load, and other factors that influence daily water needs. Today, targets have been proposed for urine osmolality, specific gravity, and color that may be used by researchers, clinicians, and individuals as simple indicators of optimal hydration. However, there remain a large number of incomplete or unanswered research questions regarding the

  17. Mesoporous Silicate Materials in Sensing

    Directory of Open Access Journals (Sweden)

    Paul T. Charles

    2008-08-01

    Full Text Available Mesoporous silicas, especially those exhibiting ordered pore systems and uniform pore diameters, have shown great potential for sensing applications in recent years. Morphological control grants them versatility in the method of deployment whether as bulk powders, monoliths, thin films, or embedded in coatings. High surface areas and pore sizes greater than 2 nm make them effective as adsorbent coatings for humidity sensors. The pore networks also provide the potential for immobilization of enzymes within the materials. Functionalization of materials by silane grafting or through cocondensation of silicate precursors can be used to provide mesoporous materials with a variety of fluorescent probes as well as surface properties that aid in selective detection of specific analytes. This review will illustrate how mesoporous silicas have been applied to sensing changes in relative humidity, changes in pH, metal cations, toxic industrial compounds, volatile organic compounds, small molecules and ions, nitroenergetic compounds, and biologically relevant molecules.

  18. The temperature hydration kinetics

    Directory of Open Access Journals (Sweden)

    Mircea Oroian

    2017-07-01

    Full Text Available The aim of this study is to evaluate the hydration kinetics of lentil seeds (Lens culinaris in water at different temperatures (25, 32.5, 40, 55, 70 and 80 °C for assessing the adequacy of models for describing the absorption phenomena during soaking. The diffusion coefficient values were calculated using Fick’s model for spherical and hemispherical geometries and the values were in the range of 10−6 m2/s. The experimental data were fitted to Peleg, Sigmoidal, Weibull and Exponential models. The models adequacy was determined using regression coefficients (R2, root mean square error (RMSE and reduced chi-square (χ2. The Peleg model is the suitable one for predicting the experimental data. Temperature had a positive and significant effect on the water absorption capacities and absorption was an endothermic process.

  19. Influence of pozzolana on C4AF hydratio n and the effects of chloride and sulfate io ns on the hydrates formed

    Directory of Open Access Journals (Sweden)

    RIMVYDAS KAMINSKAS

    2011-09-01

    Full Text Available This study investigated the influence of natural pozzolana additive on the hydration of C4AF (aluminoferrite and the effects of chloride and sulfate ions on the hydrates formed. In the samples, 25% (by weight of the C4AF was replaced with pozzolana. The mixture was then hardened for 28 days in water, soaked in a saturated NaCl solution for 3 months, and then soaked in a 5% Na2SO4 solution for 3 months at 20°C. It is estimated that under normal conditions, pozzolana additive accelerates the formation of CO32-–AFm (monocarboaluminate and gibbsite, however, impede the formation of cubic aluminum hydrates. Also, part of the amorphous SiO2 penetrates into the structure of hydrates of C4AF and initiates the formation of hydrated alumino-silicate (gismondine. Monocarboaluminate affected by NaCl becomes unstable and takes part in reactions producing Ca2Al(OH6Cl·2H2O (hydrocalumite-M. After samples were transferred from a saturated NaCl solution to a 5% Na2SO4 solution, hydrocalumite-M was the source of aluminates for the formation of ettringite. In samples with pozzolana additive, the hydrated alumino-silicate and gibbsite compounds that were formed remained stable in an environment containing chloride and sulfate ions and retarded the corrosion reaction of C4AF hydrates.

  20. Calcium Electroporation

    DEFF Research Database (Denmark)

    Frandsen, Stine Krog; Gibot, Laure; Madi, Moinecha

    2015-01-01

    BACKGROUND: Calcium electroporation describes the use of high voltage electric pulses to introduce supraphysiological calcium concentrations into cells. This promising method is currently in clinical trial as an anti-cancer treatment. One very important issue is the relation between tumor cell kill...... efficacy-and normal cell sensitivity. METHODS: Using a 3D spheroid cell culture model we have tested the effect of calcium electroporation and electrochemotherapy using bleomycin on three different human cancer cell lines: a colorectal adenocarcinoma (HT29), a bladder transitional cell carcinoma (SW780......), and a breast adenocarcinoma (MDA-MB231), as well as on primary normal human dermal fibroblasts (HDF-n). RESULTS: The results showed a clear reduction in spheroid size in all three cancer cell spheroids three days after treatment with respectively calcium electroporation (p

  1. Hydrate Phase Assemblages in Blends of Ye'elimite and Gypsum with Alite and Belite

    DEFF Research Database (Denmark)

    Pedersen, Malene Thostrup; Skibsted, Jørgen

    Calcium sulpho-aluminate (CSA) cements all contain ye’elimite, either as the main phase or in intermediate amounts, while they differ in their content of accessory phases. Belite is the main phase in most CSA cements, however, alite - CSA cements have been produced. The hydrate phases formed during...

  2. Hydrate Phase Assemblages in Blends of Ye’elimite and Gypsum with Alite and Belite

    DEFF Research Database (Denmark)

    Pedersen, Malene Thostrup; Skibsted, Jørgen

    2016-01-01

    Calcium sulpho-aluminate (CSA) cements all contain ye’elimite, either as the main phase or in intermediate amounts, while they differ in their content of accessory phases. Belite is the main phase in most CSA cements, however, alite - CSA cements have been produced. The hydrate phases formed during...

  3. Historical methane hydrate project review

    Science.gov (United States)

    Collett, Timothy; Bahk, Jang-Jun; Frye, Matt; Goldberg, Dave; Husebo, Jarle; Koh, Carolyn; Malone, Mitch; Shipp, Craig; Torres, Marta

    2013-01-01

    In 1995, U.S. Geological Survey made the first systematic assessment of the volume of natural gas stored in the hydrate accumulations of the United States. That study, along with numerous other studies, has shown that the amount of gas stored as methane hydrates in the world greatly exceeds the volume of known conventional gas resources. However, gas hydrates represent both a scientific and technical challenge and much remains to be learned about their characteristics and occurrence in nature. Methane hydrate research in recent years has mostly focused on: (1) documenting the geologic parameters that control the occurrence and stability of gas hydrates in nature, (2) assessing the volume of natural gas stored within various gas hydrate accumulations, (3) analyzing the production response and characteristics of methane hydrates, (4) identifying and predicting natural and induced environmental and climate impacts of natural gas hydrates, and (5) analyzing the effects of methane hydrate on drilling safety.Methane hydrates are naturally occurring crystalline substances composed of water and gas, in which a solid water-­‐lattice holds gas molecules in a cage-­‐like structure. The gas and water becomes a solid under specific temperature and pressure conditions within the Earth, called the hydrate stability zone. Other factors that control the presence of methane hydrate in nature include the source of the gas included within the hydrates, the physical and chemical controls on the migration of gas with a sedimentary basin containing methane hydrates, the availability of the water also included in the hydrate structure, and the presence of a suitable host sediment or “reservoir”. The geologic controls on the occurrence of gas hydrates have become collectively known as the “methane hydrate petroleum system”, which has become the focus of numerous hydrate research programs.Recognizing the importance of methane hydrate research and the need for a coordinated

  4. Silicic magmas from the Emeishan large igneous province, Southwest China: Petrogenesis and their link with the end-Guadalupian biological crisis

    Science.gov (United States)

    Xu, Yi-Gang; Chung, Sun-Lin; Shao, Hui; He, Bin

    2010-09-01

    The Emeishan large igneous province in SW China comprises a bimodal mafic-silicic suite with the silicic rocks occurring at the uppermost part of the thick lava sequence. The silicic rocks have an age of 257-263 Ma, and are thus roughly coeval with the Guadalupian-Loping (G-L) boundary event. Most silicic rocks (trachyte and rhyolite) from the Emeishan province have rather uniform ɛNd values (+ 1 to + 2.9) that are comparable with the uncontaminated high-Ti basalts. This fact and the remarkably narrow ranges of incompatible element ratios (e.g., Zr/Nb) of the basalt-silicic suite indicate a genetic relationship between basalt and silicic members. The significant difference between the Emeishan rocks and the experimental melts of hydrated basaltic crust, suggests the fractional crystallization of basaltic magma, rather than crustal melting, as the major petrogenetic process for the formation of silicic rocks. Indeed, their major and trace element trends can be modeled by fractionation of the observed mineral phases (feldspar, clinopyroxene, Fe-Ti oxide and apatite). In contrast to the virtually closed system differentiation processes associated with trachytes, the rhyolites may have experienced interaction with upper crustal material during ascent. The geochemical characteristics and recent assessment of timing of the Emeishan volcanism suggest the Emeishan rhyolites as the potential source of the widespread clay bed at the G-L boundary in south China. This enhanced the causal link between the Emeishan eruption and the end-Guadalupian biological crisis.

  5. Non-aqueous formation of the calcium carbonate polymorph vaterite: astrophysical implications

    OpenAIRE

    Day, Sarah J.; Thompson, Stephen P.; Parker, Julia E.; Evans, Aneurin

    2013-01-01

    We study the formation of calcium carbonate, through the solid-gas interaction of amorphous Ca-silicate with gaseous CO2, at elevated pressures, and link this to the possible presence of calcium carbonate in a number of circumstellar and planetary environments. We use in-situ synchrotron X-Ray powder diffraction to obtain detailed structural data pertaining to the formation of the crystalline calcium carbonate phase vaterite and its evolution with temperature. We found that the metastable cal...

  6. Alkali Silicate Vehicle Forms Durable, Fireproof Paint

    Science.gov (United States)

    Schutt, John B.; Seindenberg, Benjamin

    1964-01-01

    The problem: To develop a paint for use on satellites or space vehicles that exhibits high resistance to cracking, peeling, or flaking when subjected to a wide range of temperatures. Organic coatings will partially meet the required specifications but have the inherent disadvantage of combustibility. Alkali-silicate binders, used in some industrial coatings and adhesives, show evidence of forming a fireproof paint, but the problem of high surface-tension, a characteristic of alkali silicates, has not been resolved. The solution: Use of a suitable non-ionic wetting agent combined with a paint incorporating alkali silicate as the binder.

  7. Model Dust Envelopes Around Silicate Carbon Stars

    Directory of Open Access Journals (Sweden)

    Kyung-Won Suh

    2006-03-01

    Full Text Available We have modeled dust envelopes around silicate carbon stars using optical properties for a mixture of amorphous carbon and silicate dust grains paying close attention to the infrared observations of the stars. The 4 stars show various properties in chemistry and location of the dust shell. We expect that the objects that fit a simple detached silicate dust shell model could be in the transition phase of the stellar chemistry. For binary system objects, we find that a mixed dust chemistry model would be necessary.

  8. Characterization and nutrient release from silicate rocks and influence on chemical changes in soil

    Directory of Open Access Journals (Sweden)

    Douglas Ramos Guelfi Silva

    2012-06-01

    Full Text Available The expansion of Brazilian agriculture has led to a heavy dependence on imported fertilizers to ensure the supply of the growing food demand. This fact has contributed to a growing interest in alternative nutrient sources, such as ground silicate rocks. It is necessary, however, to know the potential of nutrient release and changes these materials can cause in soils. The purpose of this study was to characterize six silicate rocks and evaluate their effects on the chemical properties of treated soil, assessed by chemical extractants after greenhouse incubation. The experimental design consisted of completely randomized plots, in a 3 x 6 factorial scheme, with four replications. The factors were potassium levels (0-control: without silicate rock application; 200; 400; 600 kg ha-1 of K2O, supplied as six silicate rock types (breccia, biotite schist, ultramafic rock, phlogopite schist and two types of mining waste. The chemical, physical and mineralogical properties of the alternative rock fertilizers were characterized. Treatments were applied to a dystrophic Red-Yellow Oxisol (Ferralsol, which was incubated for 100 days, at 70 % (w/w moisture in 3.7 kg/pots. The soil was evaluated for pH; calcium and magnesium were extracted with KCl 1 mol L-1; potassium, phosphorus and sodium by Mehlich 1; nickel, copper and zinc with DTPA; and the saturation of the cation exchange capacity was calculated for aluminum, calcium, magnesium, potassium, and sodium, and overall base saturation. The alternative fertilizers affected soil chemical properties. Ultramafic rock and Chapada mining byproduct (CMB were the silicate rocks that most influenced soil pH, while the mining byproduct (MB led to high K levels. Zinc availability was highest in the treatments with mining byproduct and Cu in soil fertilized with Chapada and mining byproduct.

  9. Proton affinities of hydrated molecules

    Science.gov (United States)

    Valadbeigi, Younes

    2016-09-01

    Proton affinities (PA) of non-hydrated, M, and hydrated forms, M(H2O)1,2,3, of 20 organic molecules including alcohols, ethers, aldehydes, ketones and amines were calculated by the B3LYP/6-311++G(d,p) method. For homogeneous families, linear correlations were observed between PAs of the M(H2O)1,2,3 and the PAs of the non-hydrated molecules. Also, the absolute values of the hydration enthalpies of the protonated molecules decreased linearly with the PAs. The correlation functions predicted that for an amine with PA amine with PA > 1100 kJ/mol the PA(M(H2O)) is smaller than the PA.

  10. Analysis of Hydration-Mechanical-Durability Properties of Metakaolin Blended Concrete

    Directory of Open Access Journals (Sweden)

    Xiao-Yong Wang

    2017-10-01

    Full Text Available Metakaolin (MK is a highly active pozzolanic material and MK is increasingly used in producing high performance concrete. This study presents an integrated hydration-mechanical-durability model for evaluating various properties of metakaolin blended concrete. First, a blended hydration model is proposed for simulating the hydration of composite binders containing MK that considers the dilution effect and pozzolanic reaction due to metakaolin addition. The interactions between the metakaolin reaction and cement hydration were taken into account by means of the contents of calcium hydroxide and capillary water in hydrating the composite binder. The reaction degrees of cement and metakaolin were calculated using the hydration model. Second, the gel-space ratio of the MK blended concrete was determined based on the reaction degrees of the composite binders and proportions of concrete mix. Moreover, concrete compressive strength was calculated using the gel-space ratio. Third, the volumetric phase fractions were calculated based on the reaction degrees of the binders. Chloride penetrability of metakaolin blended concrete was analyzed through the capillary porosity of concrete. The proposed integrated hydration-mechanical-durability model is valuable for the material design of metakaolin blended concrete.

  11. Hydration in soccer: a review

    OpenAIRE

    Monteiro Cristiano Ralo; Guerra Isabela; Barros Turíbio Leite de

    2003-01-01

    Hydration should be considered before, during and after the exercise. This review intends to approach the main points of hydration process in soccer. The replacement of fluids during exercise is proportional to some factors, such as: exercise intensity; climatic conditions; the athlete's acclimatization; the athlete's physical conditioning; physiologic individual characteristics and the player's biomechanics. Performance is improved when players ingest not only water but also carbohydrate. Th...

  12. Mechanism of gypsum hydration

    Directory of Open Access Journals (Sweden)

    Pacheco, G.

    1991-06-01

    Full Text Available There is an hypothesis that the mechanism o f gypsum hydration and dehydration is performed through two simultaneous phenomena. In this study we try to clear up this phenomenon using chlorides as accelerators or a mixture of ethanol-methanol as retarders to carry out the gypsum setting. Natural Mexican gypsum samples and a hemihydrate prepared in the laboratory are used. The following analytical techniques are used: MO, DRX, DTA, TG and DTG. In agreement with the obtained results, it can be concluded: that colloid formation depends on the action of accelerators or retarders and the crystals are a consequence of the quantity of hemihydrate formed.

    En el mecanismo de hidratación y deshidratación del yeso existe la hipótesis de que éste se efectúa por dos fenómenos simultáneos. Este estudio intenta esclarecer estos fenómenos, empleando: cloruros como aceleradores o mezcla etanol-metanol como retardadores para efectuar el fraguado del yeso. Se emplean muestras de yeso de origen natural mexicano y hemihydrate preparado en laboratorio; se utilizan técnicas analíticas: MO, DRX, DTA, TG y DTG. De acuerdo a los resultados obtenidos se puede deducir: que la formación del coloide depende de la acción de los agentes aceleradores o retardadores y que los cristales son consecuencia de la cantidad de hemihidrato formado.

  13. Siliceous microfossil extraction from altered Monterey rocks

    Energy Technology Data Exchange (ETDEWEB)

    Nelson, C.O.; Casey, R.E.

    1986-04-01

    Samples of altered Monterey rocks of differing lithologies were processed by various methods to develop new techniques for extracting siliceous microfossils. The preliminary use of thin sections made from the same rocks reduced the number of probable samples (samples worth further processing) by about one-third. Most of the siliceous microfossils contained in altered Monterey rocks appear to be highly recrystallized and are extremely fragile; however, some contained silicified and silica-infilled radiolarians and planktonic and benthonic foraminifera, which are very tough. In general the most useful techniques were gently hydrochloric acid, hydrogen peroxide, formic acid, monosodium glutamate, and regular siliceous microfossil extraction techniques. Unsuccessful techniques and a new siliceous microfossil flotation technique are also documented.

  14. Carbon Monoxide Silicate Reduction System Project

    Data.gov (United States)

    National Aeronautics and Space Administration — The Carbon Monoxide Silicate Reduction System (COSRS) is a novel technology for producing large quantities of oxygen on the Moon. Oxygen yields of 15 kilograms per...

  15. Carbon Monoxide Silicate Reduction System Project

    Data.gov (United States)

    National Aeronautics and Space Administration — The Carbon Monoxide Silicate Reduction System (COSRS) is an innovative method that for the first time uses the strong reductant carbon monoxide to both reduce iron...

  16. Peralkaline silicic volcanic rocks in northwestern nevada.

    Science.gov (United States)

    Noble, D C; Chipman, D W; Giles, D L

    1968-06-21

    Late Tertiary silicic ashflow tuffs and lavas peralkaline in chemical character (atomic Na + K greater than Al), mainly comendites, occur over wide areas in northwestern Nevada and appear to be widespread in southeastern Oregon. Such peralkaline rocks-which are not uncommon in the western United States-and other chemically unusual silicic rocks are found near the margins rather than toward the center of the Great Basin.

  17. Thermodynamics and Kinetics of Silicate Vaporization

    Science.gov (United States)

    Jacobson, Nathan S.; Costa, Gustavo C. C.

    2015-01-01

    Silicates are a common class of materials that are often exposed to high temperatures. The behavior of these materials needs to be understood for applications as high temperature coatings in material science as well as the constituents of lava for geological considerations. The vaporization behavior of these materials is an important aspect of their high temperature behavior and it also provides fundamental thermodynamic data. The application of Knudsen effusion mass spectrometry (KEMS) to silicates is discussed. There are several special considerations for silicates. The first is selection of an appropriate cell material, which is either nearly inert or has well-understood interactions with the silicate. The second consideration is proper measurement of the low vapor pressures. This can be circumvented by using a reducing agent to boost the vapor pressure without changing the solid composition or by working at very high temperatures. The third consideration deals with kinetic barriers to vaporization. The measurement of these barriers, as encompassed in a vaporization coefficient, is discussed. Current measured data of rare earth silicates for high temperature coating applications are discussed. In addition, data on magnesium-iron-silicates (olivine) are presented and discussed.

  18. Get Enough Calcium

    Science.gov (United States)

    ... Calcium Print This Topic En español Get Enough Calcium Browse Sections The Basics Overview Foods and Vitamins ... women, don't get enough calcium. How much calcium do I need every day? Women: If you ...

  19. Calcium carbonate overdose

    Science.gov (United States)

    Tums overdose; Calcium overdose ... Calcium carbonate can be dangerous in large amounts. ... Some products that contain calcium carbonate are certain: ... and mineral supplements Other products may also contain calcium ...

  20. Clinker mineral hydration at reduced relative humidities

    DEFF Research Database (Denmark)

    Jensen, Ole Mejlhede; Hansen, Per Freiesleben; Lachowski, Eric E.

    1999-01-01

    Vapour phase hydration of purl cement clinker minerals at reduced relative humidities is described. This is relevant to modern high performance concrete that may self-desiccate during hydration and is also relevant to the quality of the cement during storage. Both the oretical considerations...... and experimental data are presented showing that C(3)A can hydrate at lower humidities than either C3S or C2S. It is suggested that the initiation of hydration during exposure to water vapour is nucleation controlled. When C(3)A hydrates at low humidity, the characteristic hydration product is C(3)AH(6...

  1. Hydration of swelling clays: multi-scale sequence of hydration and determination of macroscopic energies from microscopic properties; Hydratation des argiles gonflantes: sequence d'hydratation multi-echelle determination des energies macroscopiques a partir des proprietes microscopiques

    Energy Technology Data Exchange (ETDEWEB)

    Salles, F

    2006-10-15

    Smectites have interesting properties which make them potential candidates for engineered barriers in deep geological nuclear waste repository: low permeability, swelling and cations retention. The subject of this thesis consists in the determination of the relationship between hydration properties, swelling properties and cations mobility in relation with confinement properties of clayey materials. The aim is to understand and to predict the behaviour of water in smectites, following two research orientations: the mechanistic aspects and the energetic aspects of the hydration of smectites. We worked on the Na-Ca montmorillonite contained in the MX80 bentonite, with the exchanged homo ionic structure (saturated with alkaline cations and calcium cations). The approach crosses the various scales (microscopic, mesoscopic and macroscopic) and implied the study of the various components of the system (layer-cation-water), by using original experimental methods (thermo-poro-metry and electric conductivity for various relative humidities (RH) and electrostatic calculations. Initially, the dry state is defined by SCTA (scanning calorimetry thermal analysis). Then a classical characterization of the smectite porosity for the dry state is carried out using mercury intrusion and nitrogen adsorption. We evidenced the existence of a meso-porosity which radius varies from 2 to 10 nm depending on the compensating cation. The thermo-poro-metry and conductivity experiments performed at various hydration states made it possible to follow the increase in the pore sizes and the cations mobility as a function of the hydration state. We highlight in particular the existence of an osmotic mesoscopic swelling for low RH (approximately 50-60%RH for Li and Na). By combining the results of thermo-poro-metry, X-ray diffraction and electric conductivity, we are able to propose a complete hydration sequence for each cation, showing the crucial role of the compensating cation in the hydration of

  2. Bis(4,4'-bipyridinium) dodeca-tungsto-silicate 4,4'-bipyridine hexa-hydrate.

    Science.gov (United States)

    Ma, Feng-Xia; Zhao, Quan

    2008-09-06

    The title compound, (C(10)H(10)N(2))(2)[SiW(12)O(40)]·C(10)H(8)N(2)·6H(2)O or (4,4'-bipyH(2))(2)[SiW(12)O(40)].(4,4'-bipy)·6H(2)O (4,4'-bipy is 4,4'-bipyridine), was prepared under hydro-thermal conditions. The asymmetric unit contains a discrete Keggin-type [SiW(12)O(40)](4-) anion (located on a twofold axis), one 4,4'-bipy (located on a twofold axis), two (4,4'-bipyH(2))(2+) cations and six uncoordinated water mol-ecules. The polyoxoanion is constructed from a central SiO(4) tetra-hedron which shares its O atoms with four trinuclear W(3)O(13) groups, each of which is made up of three edge-sharing WO(6) octa-hedra. The water mol-ecules and [SiW(12)O(40)](4-) anions are linked through hydrogen bonds.

  3. Mechanical instability of monocrystalline and polycrystalline methane hydrates

    NARCIS (Netherlands)

    Wu, J.; Ning, F.; Trinh, T.T.; Kjelstrup, S.; Vlugt, T.J.H.; He, J.; Skallerud, B.H.; Zhang, Z.

    2015-01-01

    Despite observations of massive methane release and geohazards associated with gas hydrate instability in nature, as well as ductile flow accompanying hydrate dissociation in artificial polycrystalline methane hydrates in the laboratory, the destabilising mechanisms of gas hydrates under deformation

  4. Hydrated interfacial ions and electrons.

    Science.gov (United States)

    Abel, Bernd

    2013-01-01

    Charged particles such as hydrated ions and transient hydrated electrons, the simplest anionic reducing agents in water, and the special hydronium and hydroxide ions at water interfaces play an important role in many fields of science, such as atmospheric chemistry, radiation chemistry, and biology, as well as biochemistry. This article focuses on these species near hydrophobic interfaces of water, such as the air or vacuum interface of water or water protein/membrane interfaces. Ions at interfaces as well as solvated electrons have been reviewed frequently during the past decade. Although all species have been known for some time with seemingly familiar features, recently the picture in all cases became increasingly diffuse rather than clearer. The current account gives a critical state-of-the art overview of what is known and what remains to be understood and investigated about hydrated interfacial ions and electrons.

  5. Three-dimensional culture of dental pulp stem cells in direct contact to tricalcium silicate cements.

    Science.gov (United States)

    Widbiller, M; Lindner, S R; Buchalla, W; Eidt, A; Hiller, K-A; Schmalz, G; Galler, K M

    2016-03-01

    Calcium silicate cements are biocompatible dental materials applicable in contact with vital tissue. The novel tricalcium silicate cement Biodentine™ offers properties superior to commonly used mineral trioxide aggregate (MTA). Objective of this study was to evaluate its cytocompatibility and ability to induce differentiation and mineralization in three-dimensional cultures of dental pulp stem cells after direct contact with the material. Test materials included a new tricalcium silicate (Biodentine™, Septodont, Saint-Maur-des-Fossés, France), MTA (ProRoot® MTA, DENSPLY Tulsa Dental Specialities, Johnson City, TN, USA), glass ionomer (Ketac™ Molar Aplicap™, 3M ESPE, Seefeld, Germany), human dentin disks and polystyrene. Magnetic activated cell sorting for to the surface antigen STRO-1 was performed to gain a fraction enriched with mesenchymal stem cells. Samples were allowed to set and dental pulp stem cells in collagen carriers were placed on top. Scanning electron microscopy of tricalcium silicate cement surfaces with and without cells was conducted. Cell viability was measured for 14 days by MTT assay. Alkaline phosphatase activity was evaluated (days 3, 7, and 14) and expression of mineralization-associated genes (COL1A1, ALP, DSPP, and RUNX2) was quantified by real-time quantitative PCR. Nonparametric statistical analysis for cell viability and alkaline phosphatase data was performed to compare different materials as well as time points (Mann-Whitney U test, α = 0.05). Cell viability was highest on tricalcium silicate cement, followed by MTA. Viability on glass ionomer cement and dentin disks was significantly lower. Alkaline phosphatase activity was lower in cells on new tricalcium silicate cement compared to MTA, whereas expression patterns of marker genes were alike. Increased cell viability and similar levels of mineralization-associated gene expression in three-dimensional cell cultures on the novel tricalcium silicate cement and mineral

  6. Dissociation of methane hydrate granules

    Science.gov (United States)

    Misyura, S. Y.; Donskoy, I. G.; Morozov, V. S.

    2017-09-01

    The methane hydrate dissociation at negative temperatures and under external pressure of 1 bar is studied experimentally. It is shown that the dissociation rate of the gas hydrate depends on the granule diameter and heat transfer. The dissociation curve has an extremum. The dissociation rate initially increases due to the temperature increase and reaches the maximum value and then sharply falls due to the curvature of the granules. When describing dissociation kinetics of the spherical granules, it is important to take into account the granule size and their composition.

  7. Experimental Study of Methane Hydrates in Coal

    Directory of Open Access Journals (Sweden)

    Smirnov Vyacheslav

    2017-01-01

    Full Text Available The possibility of gas hydrate formation in porous space of coal has been studied. The experiments conducted have proven the possibility of methane gas hydrate formation in moist coal. It has been demonstrated that the decomposition points of methane gas hydrates in coal are near to the phase equilibrium curve for bulk methane hydrate. Only part of water absorbed by coal can be involved in the methane gas hydrate formation. With the increase in gas pressure increases the amount of gas hydrate formed in natural coal. For formation of hydrates at a positive temperature, the pressure in the system has to be at least 2 MPa. At the same time the speed of formation and decomposition of gas hydrates in coal is big enough.

  8. Calcium paradox and calcium entry blockers

    NARCIS (Netherlands)

    Ruigrok, T.J.C.; Slade, A.M.; Nayler, W.G.; Meijler, F.L.

    1984-01-01

    Reperfusion of isolated hearts with calcium-containing solution after a short period of calcium-free perfusion results in irreversible cell damage (calcium paradox). This phenomenon is characterized by an excessive influx of calcium into the cells, the rapid onset of myocardial contracture,

  9. Hydration characteristics of Biodentine and Theracal used as pulp capping materials.

    Science.gov (United States)

    Camilleri, Josette

    2014-07-01

    Investigation of the hydration and characterization of Theracal and Biodentine used for pulp capping. The setting mechanism and characterization of set Biodentine and Theracal after immersion in Hank's balanced salt solution (HBSS) for 28 days was investigated by scanning electron microscopy (SEM) of polished specimens and X-ray diffraction (XRD) analysis. The bioactivity and surface microstructure of cements immersed in HBSS or water was also assessed by similar techniques together with leaching in solution investigated by ion chromatography (IC). Biodentine hydration resulted in the formation of calcium hydroxide which was present in the material matrix and also on the material surface. Theracal was composed of large cement particles which showed some evidence of reaction rims on hydration. The material matrix included a barium zirconate phase as radiopacifier and also a glass phase composed of strontium, silicon and aluminum. This phase could not be detected in XRD analysis. Formation of a calcium phosphate phase was demonstrated on Theracal immersed in HBSS. Both materials leached calcium ions in solution. The presence of a resin matrix modifies the setting mechanism and calcium ion leaching of Theracal. The clinical implications of these findings need to be investigated. Copyright © 2014 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

  10. Methods to determine hydration states of minerals and cement hydrates

    Energy Technology Data Exchange (ETDEWEB)

    Baquerizo, Luis G., E-mail: luis.baquerizoibarra@holcim.com [Innovation, Holcim Technology Ltd., CH-5113 Holderbank (Switzerland); Matschei, Thomas [Innovation, Holcim Technology Ltd., CH-5113 Holderbank (Switzerland); Scrivener, Karen L. [Laboratory of Construction Materials, Ecole Polytechnique Fédérale de Lausanne, CH-1015 Lausanne (Switzerland); Saeidpour, Mahsa; Thorell, Alva; Wadsö, Lars [Building Materials, Lund University, Box 124, 221 000 Lund (Sweden)

    2014-11-15

    This paper describes a novel approach to the quantitative investigation of the impact of varying relative humidity (RH) and temperature on the structure and thermodynamic properties of salts and crystalline cement hydrates in different hydration states (i.e. varying molar water contents). The multi-method approach developed here is capable of deriving physico-chemical boundary conditions and the thermodynamic properties of hydrated phases, many of which are currently missing from or insufficiently reported in the literature. As an example the approach was applied to monosulfoaluminate, a phase typically found in hydrated cement pastes. New data on the dehydration and rehydration of monosulfoaluminate are presented. Some of the methods used were validated with the system Na{sub 2}SO{sub 4}–H{sub 2}O and new data related to the absorption of water by anhydrous sodium sulfate are presented. The methodology and data reported here should permit better modeling of the volume stability of cementitious systems exposed to various different climatic conditions.

  11. Polyethylene Glycol Drilling Fluid for Drilling in Marine Gas Hydrates-Bearing Sediments: An Experimental Study

    Directory of Open Access Journals (Sweden)

    Lixin Kuang

    2011-01-01

    Full Text Available Shale inhibition, low-temperature performance, the ability to prevent calcium and magnesium-ion pollution, and hydrate inhibition of polyethylene glycol drilling fluid were each tested with conventional drilling-fluid test equipment and an experimental gas-hydrate integrated simulation system developed by our laboratory. The results of these tests show that drilling fluid with a formulation of artificial seawater, 3% bentonite, 0.3% Na2CO3, 10% polyethylene glycol, 20% NaCl, 4% SMP-2, 1% LV-PAC, 0.5% NaOH and 1% PVP K-90 performs well in shale swelling and gas hydrate inhibition. It also shows satisfactory rheological properties and lubrication at temperature ranges from −8 °C to 15 °C. The PVP K-90, a kinetic hydrate inhibitor, can effectively inhibit gas hydrate aggregations at a dose of 1 wt%. This finding demonstrates that a drilling fluid with a high addition of NaCl and a low addition of PVP K-90 is suitable for drilling in natural marine gas-hydrate-bearing sediments.

  12. Early hydration cement Effect of admixtures superplasticizers

    Directory of Open Access Journals (Sweden)

    Puertas, F.

    2001-06-01

    Full Text Available Early hydration of portland cement with superplasticizer admixtures of different nature has been studied. These admixtures were: one based on melamine synthetic, other based on vinyl copolymer and other based on polyacrylate copolymers. The dosage of the formers were constant (1% weigth of cement and for the third, the influence of admixture dosage was also evaluated, giving dosage values among 1-0.3%. The pastes obtained were studied by conduction calorimetry, XRD and FTIR. Also the apparent fluidity was determined by "Minislump" test. The main results obtained were: a superplasticizers admixtures used, regardless of their nature and for the polycarboxilate one the dosage, retard the silicate hydration (specially, alite phase, b The ettringite formation is affected by the nature of the admixture. cA relationship between the dosage of admixture based on polycarboxilates and the time at the acceleration has been established. A lineal relation (y = 11.03 + 16.05x was obtained. From these results is possible to know, in function of dosage admixture, the time when the masive hydration products and the setting times are produced. Also the total heat releases in these reactions is independent of the nature and dosage of admixture, saying that in all cases the reactions are the same.

    En el presente trabajo se ha estudiado la hidratación inicial de un cemento portland aditivado con superplastificantes de diferente naturaleza. Dichos aditivos fueron: uno basado en melaminas sintéticas, otro en copolímeros vinilicos y otro en policarboxilatos. La dosificación de los dos primeros se fijó constante en 1% en peso con relación al cemento, mientras que para el tercero se evaluó, también, la influencia de la dosificación, tomando proporciones desde el 1% hasta el 0,3%. Las pastas obtenidas se estudiaron por: calorimetría de conducción, DRX y FTIR. También se determinó la fluidez de la pasta a través del ensayo del "Minislump ". Los

  13. In vitro degradation and surface bioactivity of iron-matrix composites containing silicate-based bioceramic

    Directory of Open Access Journals (Sweden)

    Sanguo Wang

    2017-03-01

    Full Text Available Iron-matrix composites with calcium silicate (CS bioceramic as the reinforcing phase were fabricated through powder metallurgy processes. The microstructures, mechanical properties, apatite deposition and biodegradation behavior of the Fe-CS composites, as well as cell attachment and proliferation on their surfaces, were characterized. In the range of CS weight percentages selected in this study, the composites possessed compact structures and showed differently decreased bending strengths as compared with pure iron. Immersion tests in simulated body fluid (SBF revealed substantially enhanced deposition of CaP on the surfaces of the composites as well as enhanced degradation rates as compared with pure iron. In addition, the composite containing 20% CS showed a superior ability to stimulate hBMSCs proliferation when compared to pure iron. Our results suggest that incorporating calcium silicate particles into iron could be an effective approach to developing iron-based biodegradable bone implants with improved biomedical performance.

  14. 77 FR 40032 - Methane Hydrate Advisory Committee

    Science.gov (United States)

    2012-07-06

    ... Methane Hydrate Advisory Committee AGENCY: Office of Fossil Energy, Department of Energy. ACTION: Notice of open meeting. SUMMARY: This notice announces a meeting of the Methane Hydrate Advisory Committee.... SUPPLEMENTARY INFORMATION: Purpose of the Committee: The purpose of the Methane Hydrate Advisory Committee is to...

  15. 78 FR 37536 - Methane Hydrate Advisory Committee

    Science.gov (United States)

    2013-06-21

    ... meeting. SUMMARY: This notice announces a meeting of the Methane Hydrate Advisory Committee. The Federal... of the Methane Hydrate Advisory Committee is to provide advice on potential applications of methane... Department of Energy's Methane Hydrate Research and Development Program. Tentative Agenda: The agenda will...

  16. Silicate mineral dissolution during heap bioleaching.

    Science.gov (United States)

    Dopson, Mark; Halinen, Anna-Kaisa; Rahunen, Nelli; Boström, Dan; Sundkvist, Jan-Eric; Riekkola-Vanhanen, Marja; Kaksonen, Anna H; Puhakka, Jaakko A

    2008-03-01

    Silicate minerals are present in association with metal sulfides in ores and their dissolution occurs when the sulfide minerals are bioleached in heaps for metal recovery. It has previously been suggested that silicate mineral dissolution can affect mineral bioleaching by acid consumption, release of trace elements, and increasing the viscosity of the leach solution. In this study, the effect of silicates present in three separate samples in conjunction with chalcopyrite and a complex multi-metal sulfide ore on heap bioleaching was evaluated in column bioreactors. Fe(2+) oxidation was inhibited in columns containing chalcopyrite samples A and C that leached 1.79 and 1.11 mM fluoride, respectively but not in sample B that contained 0.14 mM fluoride. Microbial Fe(2+) oxidation inhibition experiments containing elevated fluoride concentrations and measurements of fluoride release from the chalcopyrite ores supported that inhibition of Fe(2+) oxidation during column leaching of two of the chalcopyrite ores was due to fluoride toxicity. Column bioleaching of the complex sulfide ore was carried out at various temperatures (7-50 degrees C) and pH values (1.5-3.0). Column leaching at pH 1.5 and 2.0 resulted in increased acid consumption rates and silicate dissolution such that it became difficult to filter the leach solutions and for the leach liquor to percolate through the column. However, column temperature (at pH 2.5) only had a minor effect on the acid consumption and silicate dissolution rates. This study demonstrates the potential negative impact of silicate mineral dissolution on heap bioleaching by microbial inhibition and liquid flow. Copyright 2007 Wiley Periodicals, Inc.

  17. FORMAS DE APLICAÇÃO DE SILICATO DE CÁLCIO E MAGNÉSIO NA CULTURA DO SORGO EM NEOSSOLO QUARTZARÊNICO DE CERRADO FORMS OF APPLICATION OF CALCIUM AND MAGNESIUM SILICATE IN SORGHUM CROP IN A SAVANNAH QUARTZIPSAMMENT SOIL

    Directory of Open Access Journals (Sweden)

    Marco Aurélio Carbone Carneiro

    2008-11-01

    savannah soils are highly weathered and poor in nutrients, demanding chemical correction to  become productive. For this purpose, limestone is usually applied, but silicate sources are also used because, besides correcting soil reaction, it supplies silicon to plants. This research had as objective to evaluate the effect of  silicon levels and forms in soil and sorghum plants. Two forms of silicate application were evaluated: in the planting furrow and in the whole area. For the applications in the planting furrow, the levels of 100 kg ha-1, 200 kg ha-1, and 300 kg ha-1 of silicate were used, while for the applications in the whole area 1000 kg ha-1, 2000 kg ha-1, and 3000 kg ha-1 were used. Both application forms increased sorghum grain yield and Si concentration in soil and plants, differing, statistically, from control, but with no differences among them. The Si levels also promoted yield and Si concentration in soil and plants. The silicate addition promoted pH increase in the soil, confirming its acidity neutralization effect.

    KEY-WORDS: Silicon; silicate; sorghum.

  18. In Vitro Screening of the Apatite-Forming Ability, Biointeractivity and Physical Properties of a Tricalcium Silicate Material for Endodontics and Restorative Dentistry

    Directory of Open Access Journals (Sweden)

    Maria Giovanna Gandolfi

    2013-12-01

    Full Text Available Aim: Calcium silicate-based materials are hydraulic self-setting materials with physico-chemical properties suitable for endodontic surgery and good biological/clinical outcomes. The study aim was to evaluate the bio-properties (biointeractivity and apatite-forming ability and selected physical properties (porosity, water sorption, solubility, and setting time of Biodentine, a tricalcium silicate material for endodontics and restorative dentistry, compared to that of ProRoot MTA (Mineral Trioxide Aggregate as gold standard material. Methods: Biodentine and ProRoot MTA pastes were prepared and analyzed for calcium release and alkalinizing activity (3 h–28 days, setting time, water sorption, porosity, solubility, surface microstructure and composition, and apatite-forming ability in simulated body fluid. Results: Biodentine showed higher calcium release, alkalinizing activity, and solubility but higher open and apparent porosity, water sorption, and a markedly shorter setting time. Calcium phosphate (CaP deposits were noted on material surfaces after short ageing times. A CaP coating composed of spherulites was detected after 28 days. The thickness, continuity, and Ca/P ratio of the coating differed markedly between the materials. Biodentine showed a coating composed by denser but smaller spherulites, while ProRoot MTA showed large but less dense aggregates of spherulitic deposits. Conclusions: Biodentine showed a pronounced ability to release calcium and extended alkalinizing activity interlinked with its noticeable porosity, water sorption, and solubility: open porosities provide a broad wet biointeractive surface for the release of the calcium and hydroxyl ions involved in the formation of a CaP mineral. Biodentine is a biointeractive tricalcium silicate material with interesting chemical-physical properties and represents a fast-setting alternative to the conventional calcium silicate MTA-like cements.

  19. Hydrated-electron population dynamics

    NARCIS (Netherlands)

    Pshenichnikov, MS; Baltuska, A; Wiersma, DA; Pshenichnikov, Maxim S.; Baltuška, Andrius

    2004-01-01

    A detailed frequency-resolved pump-probe study of hydrated electron dynamics, performed with 5-fs pulses, is presented. We show that the experimental data can be successfully described with a model in which the excited state lifetime is similar to50 fs in regular water and similar to70 A in heavy

  20. Energetics of sodium-calcium exchanged zeolite A.

    Science.gov (United States)

    Sun, H; Wu, D; Guo, X; Shen, B; Navrotsky, A

    2015-05-07

    A series of calcium-exchanged zeolite A samples with different degrees of exchange were prepared. They were characterized by powder X-ray diffraction (XRD) and differential scanning calorimetry (DSC). High temperature oxide melt drop solution calorimetry measured the formation enthalpies of hydrated zeolites CaNa-A from constituent oxides. The water content is a linear function of the degree of exchange, ranging from 20.54% for Na-A to 23.77% for 97.9% CaNa-A. The enthalpies of formation (from oxides) at 25 °C are -74.50 ± 1.21 kJ mol(-1) TO2 for hydrated zeolite Na-A and -30.79 ± 1.64 kJ mol(-1) TO2 for hydrated zeolite 97.9% CaNa-A. Dehydration enthalpies obtained from differential scanning calorimetry are 32.0 kJ mol(-1) H2O for hydrated zeolite Na-A and 20.5 kJ mol(-1) H2O for hydrated zeolite 97.9% CaNa-A. Enthalpies of formation of Ca-exchanged zeolites A are less exothermic than for zeolite Na-A. A linear relationship between the formation enthalpy and the extent of calcium substitution was observed. The energetic effect of Ca-exchange on zeolite A is discussed with an emphasis on the complex interactions between the zeolite framework, cations, and water.

  1. 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.

  2. Mineralogy and Oxygen Isotope Compositions of Two C-Rich Hydrated Interplanetary Dust Particles

    Science.gov (United States)

    Snead, C. J.; McKeegan, K. D.; Messenger, S.; Nakamura-Messenger, K.

    2012-01-01

    Oxygen isotopic compositions of chondrites reflect mixing between a O-16-rich reservoir and a O-17,O-18-rich reservoir produced via mass-independent fractionation. The composition of the O-16-rich reservoir is reasonably well constrained, but material representing the O-17,O-18-rich end-member is rare. Self-shielding models predict that cometary water, presumed to represent this reservoir, should be enriched in O-17 and O-18 18O by > 200%. Hydrated interplanetary dust particles (IDPs) rich in carbonaceous matter may be derived from comets; such particles likely contain the products of reaction between O-16-poor water and anhydrous silicates that formed in the inner solar system. Here we present mineralogy and oxygen isotope compositions of two C-rich hydrated IDPs, L2083E47 and L2071E35.

  3. Modeling of Cation Binding in Hydrated 2:1 Clay Minerals - Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Smith, David E.

    2000-09-14

    Hydrated 2:1 clay minerals are high surface area, layered silicates that play a unique role in determining the fate of radionuclides in the environment. This project consisted of developing and implementing computer simulation methods for molecular characterization of the swelling and ion exchange properties of Hydrated 2:1 clay minerals, and the subsequent analysis and theoretical modeling with a view toward improving contaminant transport modeling as well as soil remediation and radionuclide containment strategies. Project results included the (a) development of simulation methods to treat clays under environmentally relevant conditions of variable water vapor pressure; (b) calculation of clay swelling thermodynamics as a function of interlayer ion size and charge (calculated quantities include immersion energies, free energies, and entropies of swelling); and (c) calculation of ion exchange free energies, including contributions from changing interlayer water contents and layer spacing.

  4. Thermal properties of methane gas hydrates

    Science.gov (United States)

    Waite, William F.

    2007-01-01

    Gas hydrates are crystalline solids in which molecules of a “guest” species occupy and stabilize cages formed by water molecules. Similar to ice in appearance (fig. 1), gas hydrates are stable at high pressures and temperatures above freezing (0°C). Methane is the most common naturally occurring hydrate guest species. Methane hydrates, also called simply “gas hydrates,” are extremely concentrated stores of methane and are found in shallow permafrost and continental margin sediments worldwide. Brought to sea-level conditions, methane hydrate breaks down and releases up to 160 times its own volume in methane gas. The methane stored in gas hydrates is of interest and concern to policy makers as a potential alternative energy resource and as a potent greenhouse gas that could be released from sediments to the atmosphere and ocean during global warming. In continental margin settings, methane release from gas hydrates also is a potential geohazard and could cause submarine landslides that endanger offshore infrastructure. Gas hydrate stability is sensitive to temperature changes. To understand methane release from gas hydrate, the U.S. Geological Survey (USGS) conducted a laboratory investigation of pure methane hydrate thermal properties at conditions relevant to accumulations of naturally occurring methane hydrate. Prior to this work, thermal properties for gas hydrates generally were measured on analog systems such as ice and non-methane hydrates or at temperatures below freezing; these conditions limit direct comparisons to methane hydrates in marine and permafrost sediment. Three thermal properties, defined succinctly by Briaud and Chaouch (1997), are estimated from the experiments described here: - Thermal conductivity, λ: if λ is high, heat travels easily through the material. - Thermal diffusivity, κ: if κ is high, it takes little time for the temperature to rise in the material. - Specific heat, cp: if cp is high, it takes a great deal of heat to

  5. Effect of curing conditions and ionic additives on properties of fly ash ...

    Indian Academy of Sciences (India)

    Administrator

    phous calcium silicate hydrate (C–S–H) as shown by Ma and Brown (1997) below. SiO2 + 1⋅7Ca(OH)2 + ... crystallized hydrated calcium silicates may form under hydrothermal conditions and form strong networks ... observed that water absorption and desorption mainly followed 1st order kinetics in case of water cured fly ...

  6. Coronary Calcium Scan

    Science.gov (United States)

    ... Back To Health Topics / Coronary Calcium Scan Coronary Calcium Scan Also known as Calcium Scan Test A coronary calcium scan is a CT scan of your heart that detects and measures the amount of calcium in the walls of your coronary arteries. Overview ...

  7. Spectroscopic investigation of cement hydrate phases and their chloride binding properties

    Science.gov (United States)

    Yu, Ping

    This thesis investigates the chloride binding properties of the hydrate phases present in Portland cement paste and the relationships between chloride binding capacity and the structure of these phases, using primarily NMR spectroscopy, infrared spectroscopy, XRD, thermal analysis, and chemical analysis. It provides important basic data and new insights into the effects of the structure of the individual hydrate phases on their chloride binding properties, and the atomic level structural states and dynamic behavior of the bound chloride in the cement hydrate crystals and at the solid/solution interface. The chloride binding capacity depends on the structure and surface properties of the individual hydrates. Portlandite and AFm surfaces have high affinity for chloride due to their positive zeta-potentials. For C-S-H samples, the chloride binding capacity increases with increasing C/S ratio due to increased numbers of surface Ca-OH sites and decreased polymerization of silicate chains. Aluminum substitution in C-S-H is unfavorable for chloride binding due to reduced layer charge and increased chain polymerization. For all hydrate phases the mechanism of chloride binding is not simply electrostatic attraction. Formation of metal-chloride clusters in the solution and sorption in the Stem layer may contribute substantially. The bound chlorides near the cement hydrate surfaces are in water solvated environments similar to those in the bulk solution and are in rapid exchange (>2kHz) with free chloride in the bulk solution. The chloride concentration near the surfaces is much higher than in the equilibrium bulk solution, and the reorientational frequency of the water molecules solvating the bound chloride is slower than those in the bulk solution. Chloride has a well-defined structural site in Friedel's salt. In solid solutions between Friedel's salt and hydroxyl-AFm, chloride occurs predominantly in Cl-rich domains except at high OH-contents.

  8. Terahertz Time Domain Spectroscopy for Structure-II Gas Hydrates

    DEFF Research Database (Denmark)

    Takeya, Kei; Zhang, Caihong; Kawayama, Iwao

    2009-01-01

    For the nondestructive inspection of gas hydrates, terahertz (THz) time-domain spectroscopy (TDS) was applied to tetrahydrofuran (THF) hydrate and propane hydrate. The absorption of propane hydrate monotonically increases with frequency, similar to the case of ice, while THF hydrate has a charact......For the nondestructive inspection of gas hydrates, terahertz (THz) time-domain spectroscopy (TDS) was applied to tetrahydrofuran (THF) hydrate and propane hydrate. The absorption of propane hydrate monotonically increases with frequency, similar to the case of ice, while THF hydrate has...

  9. A Silicate Inclusion in Puente del Zacate, a IIIA Iron Meteorite

    Science.gov (United States)

    Olsen, Edward J.; Davis, Andrew M.; Clayton, Robert N.; Mayeda, Toshiko K.; Moore, Carleton B.; Steele, Ian M.

    1996-09-01

    The IIIA and IIIB iron meteorites are considered to have formed in the cores of asteroids. A silicate inclusion within the IIIA meteorite Puente del Zacate consisting of olivine (Fa_4), low-calcium pyroxene (Fs_6Wo_1), chromium diopside (Fs_3Wo47), plagioclase (An14Or_4), graphite, troilite, chromite, daubreelite, and iron metal resembles inclusions in IAB iron meteorites. The oxygen isotopic composition of the Puente del Zacate inclusion is like chromite and phosphate inclusions in other IIIA and IIIB irons. The Puente del Zacate inclusion may have been derived from the lower mantle of the IIIAB parent asteroid.

  10. Observed gas hydrate morphologies in marine sediment

    Energy Technology Data Exchange (ETDEWEB)

    Holland, M.; Schultheiss, P.; Roberts, J.; Druce, M. [Geotek Ltd., Daventry, Northamptonshire (United Kingdom)

    2008-07-01

    The morphology of gas hydrate in marine sediments determines the basic physical properties of the sediment-hydrate matrix and provides information regarding the formation of gas hydrate deposits, and the nature of the disruption that will occur on dissociation. Small-scale morphology is useful in estimating the concentrations of gas hydrate from geophysical data. It is also important for predicting their response to climate change or commercial production. Many remote techniques for gas hydrate detection and quantification depend on hydrate morphology. In this study, morphology of gas hydrate was examined in HYACINTH pressure cores from recent seagoing expeditions. Visual and infrared observations from non-pressurized cores were also used. The expeditions and pressure core analysis were described in detail. This paper described the difference between two types of gas hydrate morphologies, notably pore-filling and grain-displacing. Last, the paper addressed the impact of hydrate morphology. It was concluded that a detailed morphology of gas hydrate is an essential component for a full understanding of the past, present, and future of any gas hydrate environment. 14 refs., 4 figs.

  11. Seismic reflections associated with submarine gas hydrates

    Energy Technology Data Exchange (ETDEWEB)

    Andreassen, K.

    1995-12-31

    Gas hydrates are often suggested as a future energy resource. This doctoral thesis improves the understanding of the concentration and distribution of natural submarine gas hydrates. The presence of these hydrates are commonly inferred from strong bottom simulating reflection (BSR). To investigate the nature of BSR, this work uses seismic studies of hydrate-related BSRs at two different locations, one where gas hydrates are accepted to exist and interpreted to be very extensive (in the Beaufort Sea), the other with good velocity data and downhole logs available (offshore Oregon). To ascertain the presence of free gas under the BSR, prestack offset data must supplement near-vertical incidence seismic data. A tentative model for physical properties of sediments partially saturated with gas hydrate and free gas is presented. This model, together with drilling information and seismic data containing the BSR beneath the Oregon margin and the Beaufort Sea, made it possible to better understand when to apply the amplitude-versus-offset (AVO) method to constrain BSR gas hydrate and gas models. Distribution of natural gas hydrates offshore Norway and Svalbard is discussed and interpreted as reflections from the base of gas hydrate-bearing sediments, overlying sediments containing free gas. Gas hydrates inferred to exist at the Norwegian-Svalbard continental margin correlate well with Cenozoic depocenters, and the associated gas is assumed to be mainly biogenic. Parts of that margin have a high potential for natural gas hydrates of both biogenic and thermogenic origin. 235 refs., 86 figs., 4 tabs.

  12. Portland cement hydration and early setting of cement stone intended for efficient paving materials

    Science.gov (United States)

    Grishina, A.

    2017-10-01

    Due to the growth of load on automotive roads, modern transportation engineering is in need of efficient paving materials. Runways and most advanced highways require Portland cement concretes. This makes important the studies directed to improvement of binders for such concretes. In the present work some peculiarities of the process of Portland cement hydration and early setting of cement stone with barium hydrosilicate sol were examined. It was found that the admixture of said sol leads to a shift in the induction period to later times without significant change in its duration. The admixture of a modifier with nanoscale barium hydrosilicates increases the degree of hydration of the cement clinker minerals and changes the phase composition of the hydration products; in particular, the content of portlandite and tricalcium silicate decreases, while the amount of ettringite increases. Changes in the hydration processes of Portland cement and early setting of cement stone that are caused by the nanoscale barium hydrosilicates, allow to forecast positive technological effects both at the stage of manufacturing and at the stage of operation. In particular, the formwork age can be reduced, turnover of molds can be increased, formation of secondary ettringite and corrosion of the first type can be eliminated.

  13. Handbook of gas hydrate properties and occurrence

    Energy Technology Data Exchange (ETDEWEB)

    Kuustraa, V.A.; Hammershaimb, E.C.

    1983-12-01

    This handbook provides data on the resource potential of naturally occurring hydrates, the properties that are needed to evaluate their recovery, and their production potential. The first two chapters give data on the naturally occurring hydrate potential by reviewing published resource estimates and the known and inferred occurrences. The third and fourth chapters review the physical and thermodynamic properties of hydrates, respectively. The thermodynamic properties of hydrates that are discussed include dissociation energies and a simplified method to calculate them; phase diagrams for simple and multi-component gases; the thermal conductivity; and the kinetics of hydrate dissociation. The final chapter evaluates the net energy balance of recovering hydrates and shows that a substantial positive energy balance can theoretically be achieved. The Appendices of the Handbook summarize physical and thermodynamic properties of gases, liquids and solids that can be used in designing and evaluating recovery processes of hydrates. 158 references, 67 figures, 47 tables.

  14. Stability constants for silicate adsorbed to ferrihydrite

    DEFF Research Database (Denmark)

    Hansen, Hans Christian Bruun; Wetche, T.P.; Raulund-Rasmussen, Karsten

    1994-01-01

    Intrinsic surface acidity constants (K(a1)intr, K(a2)intr) and surface complexation constant for adsorption of orthosilicate onto synthetic ferrihydrite (K(Si) for the complex = FeOSi(OH)3) have been determined from acid/base titrations in 0.001-0.1 m NaClO4 electrolytes and silicate adsorption e...

  15. Combustion synthesis and photoluminescence study of silicate ...

    Indian Academy of Sciences (India)

    Silicate based bioceramics are promising candidates as biomaterials for tissue engineering. The combustion synthesis method provides control on the morphology and particle size of the synthesized material. This paper discusses the combustion synthesis of akermanite (Ca2MgSi2O7 and Sr2MgSi2O7), which has been ...

  16. Well log characterization of natural gas hydrates

    Science.gov (United States)

    Collett, Timothy S.; Lee, Myung W.

    2011-01-01

    In the last 25 years we have seen significant advancements in the use of downhole well logging tools to acquire detailed information on the occurrence of gas hydrate in nature: From an early start of using wireline electrical resistivity and acoustic logs to identify gas hydrate occurrences in wells drilled in Arctic permafrost environments to today where wireline and advanced logging-while-drilling tools are routinely used to examine the petrophysical nature of gas hydrate reservoirs and the distribution and concentration of gas hydrates within various complex reservoir systems. The most established and well known use of downhole log data in gas hydrate research is the use of electrical resistivity and acoustic velocity data (both compressional- and shear-wave data) to make estimates of gas hydrate content (i.e., reservoir saturations) in various sediment types and geologic settings. New downhole logging tools designed to make directionally oriented acoustic and propagation resistivity log measurements have provided the data needed to analyze the acoustic and electrical anisotropic properties of both highly inter-bedded and fracture dominated gas hydrate reservoirs. Advancements in nuclear-magnetic-resonance (NMR) logging and wireline formation testing have also allowed for the characterization of gas hydrate at the pore scale. Integrated NMR and formation testing studies from northern Canada and Alaska have yielded valuable insight into how gas hydrates are physically distributed in sediments and the occurrence and nature of pore fluids (i.e., free-water along with clay and capillary bound water) in gas-hydrate-bearing reservoirs. Information on the distribution of gas hydrate at the pore scale has provided invaluable insight on the mechanisms controlling the formation and occurrence of gas hydrate in nature along with data on gas hydrate reservoir properties (i.e., permeabilities) needed to accurately predict gas production rates for various gas hydrate

  17. Suppressive effects of a polymer sodium silicate solution on ...

    African Journals Online (AJOL)

    The silicon contents in the roots of the miniature rose treated with polymer sodium silicate were significantly greater than that in plants treated with monomer sodium silicate. In conclusion, the suppressive effects of sodium silicate in the polymer form were confirmed against powdery mildew and root rot diseases of the ...

  18. The role of water in silicate oligomerization reaction

    NARCIS (Netherlands)

    Trinh, T.T.; Jansen, A.P.J.; Santen, R.A.; Meijer, E.J.

    2009-01-01

    The silicate oligomerization reaction is key to sol-gel chemistry and zeolite synthesis. Numerous experimental and theoretical studies have been devoted to investigating the physical chemistry of silicate oligomers in the prenucleation stage of siliceous zeolite formation. Most of the previous

  19. Suppressive effects of a polymer sodium silicate solution on ...

    African Journals Online (AJOL)

    Mohsen

    2015-10-21

    Oct 21, 2015 ... Sodium silicate was dissolved in water in either a monomer form or polymer form; the effects of both forms of sodium silicate aqueous solution on rose powdery mildew and root rot diseases of miniature rose were examined. Both forms of sodium silicate aqueous solution were applied to the roots of the.

  20. Improvement of gas hydrate preservation by increasing compression pressure to simple hydrates of methane, ethane, and propane

    Science.gov (United States)

    Kida, Masato; Jin, Yusuke; Watanabe, Mizuho; Murayama, Tetsuro; Nagao, Jiro

    2017-09-01

    In this report, we describe the dissociation behavior of gas hydrate grains pressed at 1 and 6 MPa. Certain simple gas hydrates in powder form show anomalous preservation phenomenon under their thermodynamic unstable condition. Investigation of simple hydrates of methane, ethane, and propane reveals that high pressure applied to the gas hydrate particles enhances their preservation effects. Application of high pressure increases the dissociation temperature of methane hydrate and has a restrictive effect against the dissociation of ethane and propane hydrate grains. These improvements of gas hydrate preservation by increasing pressure to the initial gas hydrate particles imply that appropriate pressure applied to gas hydrate particles enhances gas hydrate preservation effects.

  1. Search for memory effects in methane hydrate: structure of water before hydrate formation and after hydrate decomposition.

    Science.gov (United States)

    Buchanan, Piers; Soper, Alan K; Thompson, Helen; Westacott, Robin E; Creek, Jefferson L; Hobson, Greg; Koh, Carolyn A

    2005-10-22

    Neutron diffraction with HD isotope substitution has been used to study the formation and decomposition of the methane clathrate hydrate. Using this atomistic technique coupled with simultaneous gas consumption measurements, we have successfully tracked the formation of the sI methane hydrate from a water/gas mixture and then the subsequent decomposition of the hydrate from initiation to completion. These studies demonstrate that the application of neutron diffraction with simultaneous gas consumption measurements provides a powerful method for studying the clathrate hydrate crystal growth and decomposition. We have also used neutron diffraction to examine the water structure before the hydrate growth and after the hydrate decomposition. From the neutron-scattering curves and the empirical potential structure refinement analysis of the data, we find that there is no significant difference between the structure of water before the hydrate formation and the structure of water after the hydrate decomposition. Nor is there any significant change to the methane hydration shell. These results are discussed in the context of widely held views on the existence of memory effects after the hydrate decomposition.

  2. Calcium source (image)

    Science.gov (United States)

    Getting enough calcium to keep bones from thinning throughout a person's life may be made more difficult if that person has ... as a tendency toward kidney stones, for avoiding calcium-rich food sources. Calcium deficiency also effects the ...

  3. Calcium and bones (image)

    Science.gov (United States)

    Calcium is one of the most important minerals for the growth, maintenance, and reproduction of the human ... body, are continually being re-formed and incorporate calcium into their structure. Calcium is essential for the ...

  4. Calcium Pyrophosphate Deposition (CPPD)

    Science.gov (United States)

    ... Patient / Caregiver Diseases & Conditions Calcium Pyrophosphate Deposition (CPPD) Calcium Pyrophosphate Deposition (CPPD) Fast Facts The risk of ... young people, too. Proper diagnosis depends on detecting calcium pyrophosphate crystals in the fluid of an affected ...

  5. Calcium blood test

    Science.gov (United States)

    ... page: //medlineplus.gov/ency/article/003477.htm Calcium blood test To use the sharing features on this page, please enable JavaScript. The calcium blood test measures the level of calcium in the blood. ...

  6. Dipolar response of hydrated proteins

    OpenAIRE

    Matyushov, Dmitry V.

    2011-01-01

    The paper presents an analytical theory and numerical simulations of the dipolar response of hydrated proteins. The effective dielectric constant of the solvated protein, representing the average dipole moment induced at the protein by a uniform external field, shows a remarkable variation among the proteins studied by numerical simulations. It changes from 0.5 for ubiquitin to 640 for cytochrome c. The former value implies a negative dipolar susceptibility of ubiquitin, that is a dia-electri...

  7. IMPORTANCE OF HYDRATION IN SPORTS

    Directory of Open Access Journals (Sweden)

    Goran Vasić

    2008-08-01

    Full Text Available Importance of hydration is detrmined by importance of functions of water in the human organism: i.e. regulation of body temperature, transport, excretion of waste materials through urine, digestion of food which is facilititated by saliva and gastric juices, maintenance of flexibility of organs and tissues About 60 % body mass of an adult person (males: 61 %, females: 54 % is made up of water. Water content of a newly born baby reaches 77 %, and it is up to 50 % in adults. It is very important for sportsmen to provide adequate hydration during and after the time of bodily activities. A symptom of water shortage is thirst. However, thirst is a late response of an organism and it occurs when dehydration has already taken place. Minimum in take of fluids in humans should range between one-and-half to two liters. It has been known for a long time that there is no success in sport without proper hydration in a sportsman.

  8. Gas hydrates: Technology status report

    Energy Technology Data Exchange (ETDEWEB)

    1987-01-01

    In 1983, the US Department of Energy (DOE) assumed the responsibility for expanding the knowledge base and for developing methods to recover gas from hydrates. These are ice-like mixtures of gas and water where gas molecules are trapped within a framework of water molecules. This research is part of the Unconventional Gas Recovery (UGR) program, a multidisciplinary effort that focuses on developing the technology to produce natural gas from resources that have been classified as unconventional because of their unique geologies and production mechanisms. Current work on gas hydrates emphasizes geological studies; characterization of the resource; and generic research, including modeling of reservoir conditions, production concepts, and predictive strategies for stimulated wells. Complementing this work is research on in situ detection of hydrates and field tests to verify extraction methods. Thus, current research will provide a comprehensive technology base from which estimates of reserve potential can be made, and from which industry can develop recovery strategies. 7 refs., 3 figs., 6 tabs.

  9. Variation of crystal structure of hydroxyapatite in calcium phosphate cement by the substitution of strontium ions.

    Science.gov (United States)

    Wang, Xiupeng; Ye, Jiandong

    2008-03-01

    New routes were used to introduce strontium into calcium phosphate cement in the present article. The study showed that by mixing 50 wt% amorphous calcium phosphate + amorphous strontium phosphate and 50 wt% dicalcium phosphate dihydrate, hydroxyapatite and Sr-hydroxyapatite precipitated separately in the hydrated cement; whereas, by mixing 50 wt% Sr- amorphous calcium phosphate and 50 wt% dicalcium phosphate dihydrate, strontium can be doped into hydroxyapatite lattice and increase the lattice dimensions and lattice volume. The strontium substituted calcium phosphate cement has potential for use in orthopedic surgeries.

  10. Silicate grout curtains behaviour for the protection of coastal aquifers

    Energy Technology Data Exchange (ETDEWEB)

    Elektorowicz, M.; Chifrina, R.; Hesnawi, R. [Concordia Univ., Montreal, Quebec (Canada)

    1997-12-31

    Tests were performed to evaluate the behaviour of silicate grout with different reagents (ethylacetate - formamide SA and calcium chloride SC) in pure silica sand and natural soils from coastal areas containing organic matter, clayey soil and silica sand. The grouted specimens were tested with simulated fresh and salt water. The setting process during chemical grouting in the soil and sand was studied. The grouting of soil and sand with SA caused a transfer to the environment of some compounds: sodium formate, sodium acetate, ammonia and part of the initial ethylacetate and formamide. This process had a tendency to decrease for approximately 4 months. The stability of specimens was low. The grouting of soil and sand with SC caused no significant contamination of the environment. The increase of pH of environmental water was even less than with SA grouting. Also, the stability of specimens is higher in comparison with SA grouting. Salt water protected the specimens grouted with SA and SC from destruction and prevented contamination.

  11. Effects of mineral trioxide aggregate mixed with hydration accelerators on osteoblastic differentiation.

    Science.gov (United States)

    Lee, Bin-Na; Kim, Hye-Joung; Chang, Hoon-Sang; Hwang, In-Nam; Oh, Won-Mann; Kim, Jung-Woo; Koh, Jeong-Tae; Min, Kyung-San; Choi, Choong-Ho; Hwang, Yun-Chan

    2014-12-01

    Despite good physical and biological properties, mineral trioxide aggregate (MTA) has a long setting time. A hydration accelerator could decrease the setting time of MTA. This study assessed the biocompatibility of MTA mixed with hydration accelerators (calcium chloride and low-dose citric acid) and investigated the effect of these materials on osteoblast differentiation. Cell viability was evaluated by the EZ-Cytox assay kit (Daeil Lab Service, Seoul, Korea). The gene expressions of osteocalcin and bone sialoprotein were detected by reverse-transcription polymerase chain reaction and real-time polymerase chain reaction. The mineralization behavior was evaluated with alizarin red staining. There was no statistically significant difference in cell viability between experimental groups. The messenger RNA level of osteogenic genes significantly increased in MTA mixed with hydration accelerators compared with the control and MTA mixed with water. MTA mixed with the hydration accelerators resulted in similar mineralization compared with MTA mixed with water. Hydration accelerators increase the osteogenic effect and show a similar effect on the mineralization of MTA, which may have clinical applications. Copyright © 2014 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

  12. Human Dental Pulp Cells Responses to Apatite Precipitation from Dicalcium Silicates

    Directory of Open Access Journals (Sweden)

    Wei-Yun Lai

    2015-07-01

    Full Text Available Unraveling the mechanisms behind the processes of cell attachment and the enhanced proliferation that occurs as a response to the presence of calcium silicate-based materials needs to be better understood so as to expand the applications of silicate-based materials. Ions in the environment may influence apatite precipitation and affect silicate ion release from silicate-based materials. Thus, the involvement of apatite precipitate in the regulation of cell behavior of human dental pulp cells (hDPCs is also investigated in the present study, along with an investigation of the specific role of cell morphology and osteocalcin protein expression cultured on calcium silicate (CS with different Dulbecco’s modified Eagle’s medium (DMEM. The microstructure and component of CS cement immersion in DMEM and P-free DMEM are analyzed. In addition, when hDPCs are cultured on CS with two DMEMs, we evaluate fibronectin (FN and collagen type I (COL secretion during the cell attachment stage. The facilitation of cell adhesion on CS has been confirmed and observed both by scanning with an electron microscope and using immunofluorescence imaging. The results indicate that CS is completely covered by an apatite layer with tiny spherical shapes on the surface in the DMEM, but not in the P-free DMEM. Compared to the P-free DMEM, the lower Ca ion in the DMEM may be attributed to the formation of the apatite on the surfaces of specimens as a result of consumption of the Ca ion from the DMEM. Similarly, the lower Si ion in the CS-soaked DMEM is attributed to the shielding effect of the apatite layer. The P-free DMEM group releases more Si ion increased COL and FN secretion, which promotes cell attachment more effectively than DMEM. This study provides new and important clues regarding the major effects of Si-induced cell behavior as well as the precipitated apatite-inhibited hDPC behavior on these materials.

  13. Development of Alaskan gas hydrate resources

    Energy Technology Data Exchange (ETDEWEB)

    Kamath, V.A.; Sharma, G.D.; Patil, S.L.

    1991-06-01

    The research undertaken in this project pertains to study of various techniques for production of natural gas from Alaskan gas hydrates such as, depressurization, injection of hot water, steam, brine, methanol and ethylene glycol solutions through experimental investigation of decomposition characteristics of hydrate cores. An experimental study has been conducted to measure the effective gas permeability changes as hydrates form in the sandpack and the results have been used to determine the reduction in the effective gas permeability of the sandpack as a function of hydrate saturation. A user friendly, interactive, menu-driven, numerical difference simulator has been developed to model the dissociation of natural gas hydrates in porous media with variable thermal properties. A numerical, finite element simulator has been developed to model the dissociation of hydrates during hot water injection process.

  14. Anaerobic oxidation of methane above gas hydrates at Hydrate Ridge, NE Pacific Ocean

    DEFF Research Database (Denmark)

    Treude, T.; Boetius, A.; Knittel, K.

    2003-01-01

    At Hydrate Ridge (HR), Cascadia convergent margin, surface sediments contain massive gas hydrates formed from methane that ascends together with fluids along faults from deeper reservoirs. Anaerobic oxidation of methane (AOM), mediated by a microbial consortium of archaea and sulfate...

  15. Thermal conductivity of hydrate-bearing sediments

    Science.gov (United States)

    Cortes, Douglas D.; Martin, Ana I.; Yun, Tae Sup; Francisca, Franco M.; Santamarina, J. Carlos; Ruppel, Carolyn D.

    2009-01-01

    A thorough understanding of the thermal conductivity of hydrate-bearing sediments is necessary for evaluating phase transformation processes that would accompany energy production from gas hydrate deposits and for estimating regional heat flow based on the observed depth to the base of the gas hydrate stability zone. The coexistence of multiple phases (gas hydrate, liquid and gas pore fill, and solid sediment grains) and their complex spatial arrangement hinder the a priori prediction of the thermal conductivity of hydrate-bearing sediments. Previous studies have been unable to capture the full parameter space covered by variations in grain size, specific surface, degree of saturation, nature of pore filling material, and effective stress for hydrate-bearing samples. Here we report on systematic measurements of the thermal conductivity of air dry, water- and tetrohydrofuran (THF)-saturated, and THF hydrate–saturated sand and clay samples at vertical effective stress of 0.05 to 1 MPa (corresponding to depths as great as 100 m below seafloor). Results reveal that the bulk thermal conductivity of the samples in every case reflects a complex interplay among particle size, effective stress, porosity, and fluid-versus-hydrate filled pore spaces. The thermal conductivity of THF hydrate–bearing soils increases upon hydrate formation although the thermal conductivities of THF solution and THF hydrate are almost the same. Several mechanisms can contribute to this effect including cryogenic suction during hydrate crystal growth and the ensuing porosity reduction in the surrounding sediment, increased mean effective stress due to hydrate formation under zero lateral strain conditions, and decreased interface thermal impedance as grain-liquid interfaces are transformed into grain-hydrate interfaces.

  16. Clinker mineral hydration at reduced relative humidities

    DEFF Research Database (Denmark)

    Jensen, Ole Mejlhede

    1998-01-01

    This report deals with gas phase hydration of pure cement clinker minerals at reduced relative humidities. This is an important subject in relation to modern high performance concrete which may self-desiccate during hydration. In addition the subject has relevance to storage stability where...... prehydration may occur. In the report both theoretical considerations and experimental data are presented. It is suggested that the initiation of hydration during water vapour exposure is nucleation controlled....

  17. New french uranium mineral species; Nouvelles especes uraniferes francaises

    Energy Technology Data Exchange (ETDEWEB)

    Branche, G.; Chervet, J.; Guillemin, C. [Commissariat a l' Energie Atomique, Lab. du Fort de Chatillon, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1952-07-01

    In this work, the authors study the french new uranium minerals: parsonsite and renardite, hydrated phosphates of lead and uranium; kasolite: silicate hydrated of uranium and lead uranopilite: sulphate of uranium hydrated; bayleyite: carbonate of uranium and of hydrated magnesium; {beta} uranolite: silicate of uranium and of calcium hydrated. For all these minerals, the authors give the crystallographic, optic characters, and the quantitative chemical analyses. On the other hand, the following species, very rare in the french lodgings, didn't permit to do quantitative analyses. These are: the lanthinite: hydrated uranate oxide; the {alpha} uranotile: silicate of uranium and of calcium hydrated; the bassetite: uranium phosphate and of hydrated iron; the hosphuranylite: hydrated uranium phosphate; the becquerelite: hydrated uranium oxide; the curite: oxide of uranium and lead hydrated. Finally, the authors present at the end of this survey a primary mineral: the brannerite, complex of uranium titanate. (author) [French] Dans ce travail, les auteurs etudient les nouveaux mineraux uraniferes francais: parsonsite et renardite, phosphates hydrates de plomb et d'uranium; kasolite: silicate hydrate d'uranium et de plomb uranopilite: sulfate d'uranium hydrate; bayleyite: carbonate d'uranium et de magnesium hydrate; {beta} uranolite: silicate d'uranium et de calcium hydrate. Pour tous ces mineraux, les auteurs donnent les caracteres cristallographiques, optiques, et les analyses chimiques quantitatives. Par contre, les especes suivantes, tres rares dans les gites francais, n'ont pas permis d'effectuer d'analyses quantitatives. Ce sont: l'ianthinite: oxyde uraneux hydrate; l'{alpha} uranotile: silicate d'uranium et de calcium hydrate; le bassetite: phosphate d'uranium et de fer hydrate; la hosphuranylite: phosphate duranium hydrate; la becquerelite: oxyde d'uranium hydrate; la curite: oxyde d

  18. Desalination utilizing clathrate hydrates (LDRD final report).

    Energy Technology Data Exchange (ETDEWEB)

    Simmons, Blake Alexander; Bradshaw, Robert W.; Dedrick, Daniel E.; Cygan, Randall Timothy (Sandia National Laboratories, Albuquerque, NM); Greathouse, Jeffery A. (Sandia National Laboratories, Albuquerque, NM); Majzoub, Eric H. (University of Missouri, Columbia, MO)

    2008-01-01

    Advances are reported in several aspects of clathrate hydrate desalination fundamentals necessary to develop an economical means to produce municipal quantities of potable water from seawater or brackish feedstock. These aspects include the following, (1) advances in defining the most promising systems design based on new types of hydrate guest molecules, (2) selection of optimal multi-phase reactors and separation arrangements, and, (3) applicability of an inert heat exchange fluid to moderate hydrate growth, control the morphology of the solid hydrate material formed, and facilitate separation of hydrate solids from concentrated brine. The rate of R141b hydrate formation was determined and found to depend only on the degree of supercooling. The rate of R141b hydrate formation in the presence of a heat exchange fluid depended on the degree of supercooling according to the same rate equation as pure R141b with secondary dependence on salinity. Experiments demonstrated that a perfluorocarbon heat exchange fluid assisted separation of R141b hydrates from brine. Preliminary experiments using the guest species, difluoromethane, showed that hydrate formation rates were substantial at temperatures up to at least 12 C and demonstrated partial separation of water from brine. We present a detailed molecular picture of the structure and dynamics of R141b guest molecules within water cages, obtained from ab initio calculations, molecular dynamics simulations, and Raman spectroscopy. Density functional theory calculations were used to provide an energetic and molecular orbital description of R141b stability in both large and small cages in a structure II hydrate. Additionally, the hydrate of an isomer, 1,2-dichloro-1-fluoroethane, does not form at ambient conditions because of extensive overlap of electron density between guest and host. Classical molecular dynamics simulations and laboratory trials support the results for the isomer hydrate. Molecular dynamics simulations

  19. Physical Properties of Gas Hydrates: A Review

    Directory of Open Access Journals (Sweden)

    Jorge F. Gabitto

    2010-01-01

    Full Text Available Methane gas hydrates in sediments have been studied by several investigators as a possible future energy resource. Recent hydrate reserves have been estimated at approximately 1016 m3 of methane gas worldwide at standard temperature and pressure conditions. In situ dissociation of natural gas hydrate is necessary in order to commercially exploit the resource from the natural-gas-hydrate-bearing sediment. The presence of gas hydrates in sediments dramatically alters some of the normal physical properties of the sediment. These changes can be detected by field measurements and by down-hole logs. An understanding of the physical properties of hydrate-bearing sediments is necessary for interpretation of geophysical data collected in field settings, borehole, and slope stability analyses; reservoir simulation; and production models. This work reviews information available in literature related to the physical properties of sediments containing gas hydrates. A brief review of the physical properties of bulk gas hydrates is included. Detection methods, morphology, and relevant physical properties of gas-hydrate-bearing sediments are also discussed.

  20. 78 FR 26337 - Methane Hydrate Advisory Committee

    Science.gov (United States)

    2013-05-06

    ... Management's Lower 48 Assessment; Results of Consortium for Ocean Leadership Workshop; Update on International Activity; FY 2013 Methane Hydrate Program Activities and Plans; Draft Interagency Roadmap; Methane...

  1. Separation of water through gas hydrate formation

    DEFF Research Database (Denmark)

    Boch Andersen, Torben; Thomsen, Kaj

    2009-01-01

    Gas hydrate is normally recognized as a troublemaker in the oil and gas industry. However, gas hydrate has some interesting possibilities when used in connection with separation of water. Nordic Sugar has investigated the possibility of using gas hydrates for concentration of sugar juice. The goal...... of the project was to formulate an alternative separation concept, which can replace the traditional water evaporation process in the sugar production. Work with the separation concept showed that gas hydrates can be used for water separation. The process is not suitable for sugar production because of large...

  2. Observations related to tetrahydrofuran and methane hydrates for laboratory studies of hydrate-bearing sediments

    Science.gov (United States)

    Lee, J.Y.; Yun, T.S.; Santamarina, J.C.; Ruppel, C.

    2007-01-01

    The interaction among water molecules, guest gas molecules, salts, and mineral particles determines the nucleation and growth behavior of gas hydrates in natural sediments. Hydrate of tetrahydrofuran (THF) has long been used for laboratory studies of gas hydrate-bearing sediments to provide close control on hydrate concentrations and to overcome the long formation history of methane hydrate from aqueous phase methane in sediments. Yet differences in the polarizability of THF (polar molecule) compared to methane (nonpolar molecule) raise questions about the suitability of THF as a proxy for methane in the study of hydrate-bearing sediments. From existing data and simple macroscale experiments, we show that despite its polar nature, THF's large molecular size results in low permittivity, prevents it from dissolving precipitated salts, and hinders the solvation of ions on dry mineral surfaces. In addition, the interfacial tension between water and THF hydrate is similar to that between water and methane hydrate. The processes that researchers choose for forming hydrate in sediments in laboratory settings (e.g., from gas, liquid, or ice) and the pore-scale distribution of the hydrate that is produced by each of these processes likely have a more pronounced effect on the measured macroscale properties of hydrate-bearing sediments than do differences between THF and methane hydrates themselves.

  3. Waters of Hydration of Cupric Hydrates: A Comparison between Heating and Absorbance Methods

    Science.gov (United States)

    Barlag, Rebecca; Nyasulu, Frazier

    2011-01-01

    The empirical formulas of four cupric hydrates are determined by measuring the absorbance in aqueous solution. The Beer-Lambert Law is verified by constructing a calibration curve of absorbance versus known Cu[superscript 2+](aq) concentration. A solution of the unknown hydrate is prepared by using 0.2-0.3 g of hydrate, and water is added such…

  4. Experimental Evaluation of Sodium Silicate-Based Nanosilica against Chloride Effects in Offshore Concrete

    Directory of Open Access Journals (Sweden)

    Kyoung-Min Kim

    2014-01-01

    Full Text Available This study investigates the effect of a new pore filling material, named sodium silicate-based nanosilica (SS, on resisting the diffusion of the chloride ions. The proposed SS is chosen, mainly due to its smaller particle size, compared to the conventional ethyl silicate-based nanosilica. Each particle of SS is chemically treated to have the negative (− charge on its surface. Four types of mixes with different amounts of partial replacement with fly ash and slag are prepared. Effect of water to binder ratios (0.35, 0.40, and 0.45 is also examined. Test results showed that the inclusion of SS was significantly beneficial for protecting the concrete from chloride attack. At a given strength, the SS inclusion in concrete was up to three times more effective than the control concrete without SS. It is believed that these excellent results are attributed to the small particle size and the chemical surface treatment of SS. In this study, experiments of compressive strength, hydration heat, accelerated neutralization, and sulfate erosion tests were also conducted to find the general effect of SS inclusion on the fundamental properties and durability of concrete.

  5. Assessing the mineralogy and hydration of rocky cores of satellites: insights from experiments and thermodynamics

    Science.gov (United States)

    Reynard, B.; Neri, A.; Sotin, C.

    2016-12-01

    Icy satellites and similar objects likely form from a mixture of hydrated rocky material, such as the CI chondrites, and various amounts of ices. Mass-balance estimates show that hydrous silicates such as serpentine, and brucite, the simple Mg-Fe hydroxide, dominate fully hydrated mineralogy. The inferred iron content of these minerals is, however, very dependent on assumptions of iron redox state, and whether it forms sulfides or segregates into a metal core. From the determination of the moment of inertia inferred from gravity measurements at Jupiter and Saturn by the Galileo and Cassini spacecraft, Ganymede and Europa would have a differentiated iron-rich core whereas Titan and Enceladus would not. Whatever the case, iron content is generally significantly higher than that of the terrestrial ultrabasic rocks used as analogs in modeling of hydrated satellite cores. Thus, we investigated the phase relations of iron-rich ultrabasic systems based on chondritic composition by combining thermodynamic modeling and preliminary high-pressure experiments. Our starting composition model is that of CI carbonaceous chondrites. Stable mineral assemblages are calculated with the PerpleX package (Connolly, 1990), assuming excess water, and various amounts of iron in the silicate phase through varying the amount of iron sulfide (troilite) or iron oxide (magnetite). Results show stable hydrated minerals are serpentine, chlorite, brucite, Na-phlogopite and in extreme cases, talc in the 1.5-5 GPa range relevant to bodies larger than about 1000 km in radius. Dehydration temperatures are extremely sensitive to the iron content, hence on the chosen amount of iron bearing phase (troilite or magnetite), and to a lower extent on average CI composition. An experimental approach was developed to simulate hydrous alteration of CI-like material. A mixture of synthetic silicates, troilite, and organic compounds, to which excess water is added, is used. Mineralogy and composition is checked

  6. Hydration in soccer: a review

    Directory of Open Access Journals (Sweden)

    Monteiro Cristiano Ralo

    2003-01-01

    Full Text Available Hydration should be considered before, during and after the exercise. This review intends to approach the main points of hydration process in soccer. The replacement of fluids during exercise is proportional to some factors, such as: exercise intensity; climatic conditions; the athlete's acclimatization; the athlete's physical conditioning; physiologic individual characteristics and the player's biomechanics. Performance is improved when players ingest not only water but also carbohydrate. The rates that carbohydrate and water are absorbed by the organism are limited by the rates of gastric emptying and intestinal absorption. The composition of drinks offered to the players should be influenced by the relative importance of the need of supplying carbohydrates or water; it should be remembered that the depletion of carbohydrate can result in fatigue and decrease of performance, but it is not usually a life-threatening condition. The addition of carbohydrate in these drinks increases the concentrations of blood glucose, increases the use of external fuel through the increase of the glucose oxidation in the muscles and it spares muscle glycogen. So, the ingestion of carbohydrate before and during the exercise can delay the emergence of fatigue and increase the players' performance. Several tactics can be used to avoid dehydration, like hyperhydration before exercise and player's acclimatization. The ideal situation to restore the player's fluid losses is between the sessions of exercises. Since soccer is a sport with quite peculiar characteristics related to hydration, the players should be concerned and educated about the importance of fluid ingestion before, during and after the exercise.

  7. IMPORTANCE OF HYDRATION IN SPORTS

    OpenAIRE

    Goran Vasić; Dragoslav Jakonić

    2008-01-01

    Importance of hydration is detrmined by importance of functions of water in the human organism: i.e. regulation of body temperature, transport, excretion of waste materials through urine, digestion of food which is facilititated by saliva and gastric juices, maintenance of flexibility of organs and tissues About 60 % body mass of an adult person (males: 61 %, females: 54 %) is made up of water. Water content of a newly born baby reaches 77 %, and it is up to 50 % in adults. It is very importa...

  8. Hydration recommendations for sport 2008.

    Science.gov (United States)

    Montain, Scott J

    2008-01-01

    Fluid replacement remains an important strategy for preserving exercise performance as dehydration in excess of 2% of body weight consistently impairs aerobic exercise performance. Too much of a good thing, however, can have negative health consequences as persistent drinking in excess of sweating rate can induce symptomatic exercise associated hyponatremia. This short review highlights new position stands and/or policy statements regarding fluid replacement for sport, evidence that laboratory findings translate to team sport performance, and current hydration practices of athletes. It is culminated with practical strategies for drinking appropriately during physical activity.

  9. Influence of composition on setting kinetics of new injectable and/or fast setting tricalcium silicate cements.

    Science.gov (United States)

    Setbon, H M; Devaux, J; Iserentant, A; Leloup, G; Leprince, J G

    2014-12-01

    New commercial tricalcium silicate based cements were elaborated to improve handling properties and setting time. The goals of the present work were: (i) to determine the composition of the new injectable and/or fast setting calcium silicate based cements, and (ii) to investigate the impact of the differences in composition on their setting kinetics. The materials considered were Angelus MTA™, Biodentine™, MM-MTA™, MTA-Caps™, and ProRoot MTA™ as control. Elemental composition of materials was studied by Inductively Coupled Plasma-Atomic Emission Spectroscopy and X-ray Energy Dispersive analysis, whereas phases in presence were analyzed by Micro-Raman spectroscopy and X-ray Diffraction analysis and cement surface by Scanning Electron Microscope. Setting kinetics was evaluated using rheometry. Elemental analysis revealed, for all cements, the presence of three major components: calcium, silicon and oxygen. Chlorine was detected in MM-MTA, MTA-Caps and Biodentine. Different radio-opacifiers were identified: bismuth oxide in ProRoot MTA, Angelus MTA and MM-MTA, zirconium oxide in Biodentine and calcium tungstate (CaWO4) in MTA-Caps. All cements were composed of di- and tri-calcium silicate, except Biodentine for which only the latter was detected. Major differences in setting kinetics were observed: a modulus of 8×10(8)Pa is reached after 12min for Biodentine, 150min for MM-MTA, 230min for Angelus MTA and 320min for ProRoot MTA. The maximum modulus reached by MTA-Caps was 7×10(8)Pa after 150min. Even if these cements possess some common compounds, major differences in their composition were observed between them, which directly influence their setting kinetics. Copyright © 2014 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

  10. Níveis de silicato de cálcio e magnésio na produção das gramídeas Marandu e Tanzânia cultivadas em um Neossolo Quartzarênico Level of calcium and magnesium silicate in the yield of Marandu grass and Tanzania grass cultivated in one Quartzsandy Neosoil

    Directory of Open Access Journals (Sweden)

    Caio Augustus Fortes

    2008-02-01

    Full Text Available O estudo foi conduzido em casa-de-vegetação do Departamento de Ciência do Solo da Universidade Federal de Lavras, Lavras-MG, com o objetivo de avaliar o efeito da correção da acidez do solo, por meio da aplicação de níveis de silicato de Ca e Mg, na produção das gramíneas Brachiaria brizantha cv. Marandu e Panicum maximum cv. Tanzânia-1 cultivadas em solo Neossolo Quartzarênico ortic. O delineamento experimental utilizado foi blocos ao acaso, em esquema fatorial 2 x 5 com quatro repetições, sendo duas forrageiras e cinco níveis de saturação por bases (V% original, 40, 60, 80 e 100%. Cada unidade experimental correspondeu a um vaso sem furos, com capacidade para 4,0 dm³ de solo, totalizando 40 vasos. Foram avaliadas as produções de MS por corte (PMS e total (PTMS, a altura e o número de perfilhos. Não houve variação entre as gramíneas em altura de perfilhos. O Tanzânia foi superior ao Marandu em PMS e número de perfilhos. Houve aumento linear na PMS, PTMS e altura de perfilhos. Conclui-se que ambas as gramíneas responderam de forma positiva à elevação dos níveis de V%, em PMS, até 54,8%. O Tanzânia produziu mais MS em relação ao Marandu.This study was conducted in a greenhouse of the Soil Science Department at Universidade Federal de Lavras, Lavras-MG, with the purpose of evaluating the effect of the soil correction acidity, by the application of Ca and Mg silicate levels, in the production of grasses Brachiaria brizantha cv. Marandu and Panicum maximum cv. Tanzânia-1 cultivated in Quartzsandy Neosoil ortic. The experimental design was a randomized complete block, in 2 x 5 factorial scheme with four replicates, being two forages and five levels of base saturation (BS%; (original BS, 40, 60, 80 and 100%. Each experimental unit corresponded to a pot with a capacity of 4.0 dm³ of soil, totalizing 40 pots. The dry matter yield (DMY for cut and total (TDMY, height and number of tillers were evaluated. There were

  11. Effects of Nanosilica on Early Age Stages of Cement Hydration

    OpenAIRE

    Forood Torabian Isfahani; Elena Redaelli; Weiwen Li; Yaru Sun

    2017-01-01

    Effects of nanosilica on cement hydration have been broadly investigated in the literature and early age cement hydration, as a whole, has been mainly considered, disregarding the substages of the hydration. The hydration of cement is characterized by different substages and nanosilica effect on the hydration could be a result of diverse, even contradictory, behavior of nanosilica in individual stages of the hydration. In this study, effects of nanosilica on different substages of cement hydr...

  12. In-situ early-age hydration study of sulfobelite cements by synchrotron powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Álvarez-Pinazo, G.; Cuesta, A.; García-Maté, M.; Santacruz, I.; Losilla, E.R. [Departamento de Química Inorgánica, Universidad de Málaga, Campus Teatinos S/N., 29071 Málaga (Spain); Sanfélix, S.G. [Unidad Técnica de Investigación de Materiales, AIDICO, Avda. Benjamín Franklin, 17 Paterna, Valencia (Spain); Fauth, F. [CELLS-Alba synchrotron, Carretera BP 1413, Km. 3.3, E-08290 Cerdanyola, Barcelona (Spain); Aranda, M.A.G. [Departamento de Química Inorgánica, Universidad de Málaga, Campus Teatinos S/N., 29071 Málaga (Spain); CELLS-Alba synchrotron, Carretera BP 1413, Km. 3.3, E-08290 Cerdanyola, Barcelona (Spain); De la Torre, A.G., E-mail: mgd@uma.es [Departamento de Química Inorgánica, Universidad de Málaga, Campus Teatinos S/N., 29071 Málaga (Spain)

    2014-02-15

    Eco-friendly belite calcium sulfoaluminate (BCSA) cement hydration behavior is not yet well understood. Here, we report an in-situ synchrotron X-ray powder diffraction study for the first hours of hydration of BCSA cements. Rietveld quantitative phase analysis has been used to establish the degree of reaction (α). The hydration of a mixture of ye'elimite and gypsum revealed that ettringite formation (α ∼ 70% at 50 h) is limited by ye'elimite dissolution. Two laboratory-prepared BCSA cements were also studied: non-active-BCSA and active-BCSA cements, with β- and α′{sub H}-belite as main phases, respectively. Ye'elimite, in the non-active-BCSA system, dissolves at higher pace (α ∼ 25% at 1 h) than in the active-BCSA one (α ∼ 10% at 1 h), with differences in the crystallization of ettringite (α ∼ 30% and α ∼ 5%, respectively). This behavior has strongly affected subsequent belite and ferrite reactivities, yielding stratlingite and other layered phases in non-active-BCSA. The dissolution and crystallization processes are reported and discussed in detail. -- Highlights: •Belite calcium sulfoaluminate cements early hydration mechanism has been determined. •Belite hydration strongly depends on availability of aluminum hydroxide. •Orthorhombic ye’elimite dissolved at a higher pace than cubic one. •Ye’elimite larger reaction degree yields stratlingite formation by belite reaction. •Rietveld method quantified gypsum, anhydrite and bassanite dissolution rates.

  13. Nutrition and hydration concerns of the female football player.

    Science.gov (United States)

    Maughan, Ronald J; Shirreffs, Susan M

    2007-08-01

    There is little information on the nutritional habits of female football players at any level of the game. There is also a shortage of information on the nutrition and hydration strategies that players should adopt. In general, differences in nutritional needs between males and females are smaller than differences between individuals, so that principles developed for male players also apply to women. There is a need to address energy balance and body composition: prolonged energy deficits cannot be sustained without harm to health and performance. Published reports show mean carbohydrate intakes for female players of about 5 g/kg/day, and this seems to be too low to sustain consistent intensive training. The timing of protein intake may be as important as the amounts consumed, provided that the total intake is adequate. Dehydration adversely affects skill and stamina in women as it does in men, so an individualised hydration strategy should be developed. The prevalence of iron deficiency in women generally is high, but it seems to be alarmingly high in female players. All players should adopt dietary habits that ensure adequate iron intake. Football training seems to increase bone mass in the weight-bearing limbs, with positive implications for bone health in later life, but some players may be at risk from inadequate calcium dietary intake.

  14. Experimental observations on the competing effect of tetrahydrofuran and an electrolyte and the strength of hydrate inhibition among metal halides in mixed CO{sub 2} hydrate equilibria

    Energy Technology Data Exchange (ETDEWEB)

    Sabil, Khalik M., E-mail: khalik_msabil@petronas.com.m [Delft University of Technology, Laboratory of Process Equipment, Mechanical, Maritime and Materials Engineering, Leeghwaterstraat 44, 2628 CA Delft (Netherlands); Universiti Teknologi PETRONAS, Chemical Engineering Programme, Bandar Seri Iskandar, 31750 Tronoh, Perak (Malaysia); Roman, Vicente R.; Witkamp, Geert-Jan [Delft University of Technology, Laboratory of Process Equipment, Mechanical, Maritime and Materials Engineering, Leeghwaterstraat 44, 2628 CA Delft (Netherlands); Peters, Cor J., E-mail: C.J.Peters@tudelft.n [Delft University of Technology, Laboratory of Process Equipment, Mechanical, Maritime and Materials Engineering, Leeghwaterstraat 44, 2628 CA Delft (Netherlands); Petroleum Institute, Chemical Engineering Program, Bu Hasa Building, Room 2207A, P.O. Box 2533, Abu Dhabi (United Arab Emirates)

    2010-03-15

    In the present work, experimental data on the equilibrium conditions of mixed CO{sub 2} and THF hydrates in aqueous electrolyte solutions are reported. Seven different electrolytes (metal halides) were used in this work namely sodium chloride (NaCl), calcium chloride (CaCl{sub 2}), magnesium chloride (MgCl{sub 2}), potassium bromide (KBr), sodium fluoride (NaF), potassium chlorid