WorldWideScience

Sample records for calcium carbonate deposition

  1. Studies on structure and organization of calcium carbonate deposits in algae

    Digital Repository Service at National Institute of Oceanography (India)

    Kerkar, V.; Untawale, A.G.

    The structure and organization of calcium carbonate deposits is studied in species of Halimeda, Udotea, Neomeris (Chlorophyta) and Padina (Phaeophyta). It was found that in Halimeda aragonite deposition takes place outside the cell wall...

  2. Chitosan Derivatives/Calcium Carbonate Composite Capsules Prepared by the Layer-by-Layer Deposition Method

    Directory of Open Access Journals (Sweden)

    Takashi Sasaki

    2008-01-01

    Full Text Available Core/shell capsules composed of calcium carbonate whisker core (rod-like shape and chitosan/chitosansulfate shell were prepared by the layer-by-layer deposition technique. Two chitosan samples of different molecular weights (Mw=9.7×104 and 1.09×106g·mol-1 were used as original materials. Hollow capsules were also obtained by dissolution of the core in hydrochloric acid. Electron microscopy revealed that the surface of the shell is rather ragged associated with some agglomerates. The shell thickness l obeys a linear relation with respect to the number of deposited layers m as l=md+a(a>0. The values of d (thickness per layer were 4.0 and 1.0 nm for the higher and lower Mw chitosan materials, respectively, both of which are greater than the thickness of the monolayer. The results suggest that the feature of the deposition does not obey an ideal homogeneous monolayer-by-monolayer deposition mechanism. Shell crosslinked capsules were also prepared via photodimerization reaction of cinnamoyl groups after a deposition of cinnamoyl chitosan to the calcium carbonate whisker core. The degree of crosslink was not enough to stabilize the shell structure, and hollow capsule was not obtained.

  3. Calcium Carbonate

    Science.gov (United States)

    ... doctor if you have or have ever had kidney disease or stomach conditions.tell your doctor if you are pregnant, plan to become pregnant, or are breast-feeding. If you become pregnant while taking calcium carbonate, call your doctor.

  4. Deposition of calcium carbonate in karst caves: role of bacteria in Stiffe's cave.

    Directory of Open Access Journals (Sweden)

    Ercole Claudia

    2001-01-01

    Full Text Available Bacteria make a significant contribution to the accumulation of carbonate in several natural habitats where large amounts of carbonates are deposited. However, the role played by microbial communities in speleothem formation (stalactites, stalagmites etc. in caves is still unclear. In bacteria carbonate is formed by autotrophic pathways, which deplete CO2 from the environment, and by heterotrophic pathways, leading to active or passive precipitation. We isolated cultivable heterotrophic microbial strains, able to induce CaCO3 precipitation in vitro, from samples taken from speleothems in the galleries of Stiffe’s cave, L’Aquila, Italy. We found a large number of bacteria in the calcite formations (1 x 104 to 5 x 109 cells g-1. Microscopic examination, in laboratory conditions at different temperatures, showed that most of the isolates were able to form calcium carbonate microcrystals. The most crystalline precipitates were observed at 32°C. No precipitation was detected in un-inoculated controls media or in media that had been inoculated with autoclaved bacterial cells. X-ray diffraction (XRD analysis showed that most of the carbonate crystals produced were calcite. Bacillus strains were the most common calcifying isolates collected from Stiffe’s Cave. Analysis of carbonate-solubilization capability revealed that the non-calcifying bacteria were carbonate solubilizers.

  5. Deposition of calcium carbonate films by a polymer-induced liquid-precursor (PILP) process

    Science.gov (United States)

    Gower, Laurie B.; Odom, Damian J.

    2000-03-01

    A polypeptide additive has been used to transform the solution crystallization of calcium carbonate to a solidification process of a liquid-phase mineral precursor. In situ observations reveal that polyaspartate induces liquid-liquid phase separation of droplets of a mineral precursor. The droplets deposit on the substrate and coalesce to form a coating, which then solidifies into calcitic tablets and films. Transition bars form during the amorphous to crystalline transition, leading to sectorization of calcite tablets, and the defect textures and crystal morphologies are atypical of solution grown crystals. The formation of nonequilibrium crystal morphologies using an acidic polypeptide may have implications in the field of biomineralization, and the environmentally friendly aspects of this polymer-induced liquid-precursor (PILP) process may offer new techniques for aqueous-based processing of ceramic films, coatings, and particulates.

  6. Lab-Scale Study of the Calcium Carbonate Dissolution and Deposition by Marine Cyanobacterium Phormidium subcapitatum

    Science.gov (United States)

    Karakis, S. G.; Dragoeva, E. G.; Lavrenyuk, T. I.; Rogochiy, A.; Gerasimenko, L. M.; McKay, D. S.; Brown, I. I.

    2006-01-01

    Suggestions that calcification in marine organisms changes in response to global variations in seawater chemistry continue to be advanced (Wilkinson, 1979; Degens et al. 1985; Kazmierczak et al. 1986; R. Riding 1992). However, the effect of [Na+] on calcification in marine cyanobacteria has not been discussed in detail although [Na+] fluctuations reflect both temperature and sea-level fluctuations. The goal of these lab-scale studies therefore was to study the effect of environmental pH and [Na+] on CaCO3 deposition and dissolution by marine cyanobacterium Phormidium subcapitatum. Marine cyanobacterium P. subcapitatum has been cultivated in ASN-III medium. [Ca2+] fluctuations were monitored with Ca(2+) probe. Na(+) concentrations were determined by the initial solution chemistry. It was found that the balance between CaCO3 dissolution and precipitation induced by P. subcapitatum grown in neutral ASN III medium is very close to zero. No CaCO3 precipitation induced by cyanobacterial growth occurred. Growth of P. subcapitatum in alkaline ASN III medium, however, was accompanied by significant oscillations in free Ca(2+) concentration within a Na(+) concentration range of 50-400 mM. Calcium carbonate precipitation occurred during the log phase of P. subcapitatum growth while carbonate dissolution was typical for the stationary phase of P. subcapitatum growth. The highest CaCO3 deposition was observed in the range of Na(+) concentrations between 200-400 mM. Alkaline pH also induced the clamping of P. subcapitatum filaments, which appeared to have a strong affinity to envelop particles of chemically deposited CaCO3 followed by enlargement of those particles size. EDS analysis revealed the presence of Mg-rich carbonate (or magnesium calcite) in the solution containing 10-100 mM Na(+); calcite in the solution containing 200 mM Na(+); and aragonite in the solution containing with 400 mM Na(+). Typical present-day seawater contains xxmM Na(+). Early (Archean) seawater was

  7. Study of the effect of magnesium concentration on the deposit of allotropic forms of calcium carbonate and related carbon steel interface behavior

    Energy Technology Data Exchange (ETDEWEB)

    Ben Amor, Y., E-mail: yasser_ben@yahoo.f [Institut Superieur des Sciences et Technologies de l' Environnement de Borj-Cedria, B.P 1003, Hammam-Lif 2050 (Tunisia); Bousselmi, L. [Laboratoire Traitement et Recyclage des Eaux, B.P 273, Hammam-Lif, Technopole de Borj-Cedria, 8020 Soliman (Tunisia); Tribollet, B. [UPR 15 CNRS - Physique des liquides et Electrochimie, Universite Pierre et Marie Curie - Tour 22, 4 place Jussieu, 75252 Paris Cedex 05 (France); Triki, E. [Unite de recherche Corrosion et Protection des metalliques, Ecole Nationale d' Ingenieurs de Tunis, P.B. 37, 1002 Tunis, Belvedere (Tunisia)

    2010-06-30

    Different allotropic forms of calcium carbonate scales were electrochemically deposited on a carbon steel surface in artificial underground Tunisian water at -0.95 V{sub SCE} and various Mg{sup 2+} concentrations. Because of the importance of the diffusion process, the rotating disk electrode was used. The deposition kinetics were analyzed by chronoamperometry measurements and the calcareous layers were characterized by electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM). The physical model proposed by Gabrielli was used to analyze the EIS measurements. Independent of the deposited allotropic form of calcium carbonate, the measurements showed that the oxygen reduction occurs in the pores formed between the CaCO{sub 3} crystals and the metallic surface.

  8. Depositional environments inferred from variations of calcium carbonate, organic carbon, and sulfide sulfur: a core from southeastern Arabian Sea

    Digital Repository Service at National Institute of Oceanography (India)

    Paropkari, A; Iyer, S.D.; Chauhan, O; PrakashBabu, C.

    The variations in CaCO3 and organic carbon and their inter-relationship in a core from the southeastern Arabian Sea (water depth 2,212 m) have been used to demarcate the Holocene/Pleistocene boundary; an increased terrigenous deposition during Late...

  9. Carbon nanotubes play an important role in the spatial arrangement of calcium deposits in hydrogels for bone regeneration.

    Science.gov (United States)

    Cancian, Giulia; Tozzi, Gianluca; Hussain, Amirul Ashraf Bin; De Mori, Arianna; Roldo, Marta

    2016-08-01

    Age related bone diseases such as osteoporosis are considered among the main causes of reduced bone mechanical stability and bone fractures. In order to restore both biological and mechanical function of diseased/fractured bones, novel bioactive scaffolds that mimic the bone structure are constantly under development in tissue engineering applications. Among the possible candidates, chitosan-based thermosensitive hydrogel scaffolds represent ideal systems due to their biocompatibility, biodegradability, enhanced antibacterial properties, promotion of osteoblast formation and ease of injection, which makes them suitable for less invasive surgical procedures. As a main drawback, these chitosan systems present poor mechanical performance that could not support load-bearing applications. In order to produce more mechanically-competent biomaterials, the combined addition of hydroxyapatite and carbon nanotubes (CNTs) is proposed in this study. Specifically, the aim of this work is to develop thermosensitive chitosan hydrogels containing stabilised single-walled and multi-walled CNTs, where their effect on the mechanical/physiochemical properties, calcium deposition patterns and ability to provide a platform for the controlled release of protein drugs was investigated. It was found that the addition of CNTs had a significant effect on the sol-gel transition time and significantly increased the resistance to compression for the hydrogels. Moreover, in vitro calcification studies revealed that CNTs played a major role in the spatial arrangements of newly formed calcium deposits in the composite materials studied, suggesting that they may have a role in the way the repair of fragile and/or fractured bones occurs in vivo.

  10. CRACK2. Modelling calcium carbonate deposition from bicarbonate solutions in cracks in concrete

    DEFF Research Database (Denmark)

    Brodersen, Knud Erik

    2003-01-01

    The numerical CRACK2 model simulates precipitation of calcite from calcium bicarbonate solution (e.g. groundwater) passing through cracks in concrete or other cementitious materials. A summary of experimental work is followed by a detailed description ofthe model. Hydroxyl ions are transported...... by diffusion in pore systems in columns of cementitious materials. The hydroxyl is precipitating calcite from a flow of bicarbonate solution in a crack connecting the ends of a row of such columns. Thecementitious material is simulated as calcium hydroxide mixed with inert material but with sodium hydroxide...... dissolved in the pore solution. Diffusive migration of cesium as radioactive isotope is also considered. Electrical interaction of the migratingions is taken into account. Example calculations demonstrate effects of parameter variations on distribution of precipitated calcite in the crack...

  11. CRACK2 - Modelling calcium carbonate deposition from bicarbonate solution in cracks in concrete

    Energy Technology Data Exchange (ETDEWEB)

    Brodersen, K

    2003-03-01

    The numerical CRACK2 model simulates precipitation of calcite from calcium bicarbonate solution (e.g. groundwater) passing through cracks in concrete or other cementitious materials. A summary of experimental work is followed by a detailed description of the model. Hydroxyl ions are transported by diffusion in pore systems in columns of cementitious materials. The hydroxyl is precipitating calcite from a flow of bicarbonate solution in a crack connecting the ends of a row of such columns. The cementitious material is simulated as calcium hydroxide mixed with inert material but with sodium hydroxide dissolved in the pore solution. Diffusive migration of cesium as radioactive isotope is also considered. Electrical interaction of the migrating ions is taken into account. Example calculations demonstrate effects of parameter variations on distribution of precipitated calcite in the crack and on the composition of the outflowing solution, which can be compared directly with experimental results. Leaching behavior of sodium can be used to tune the model to experimental observations. The calcite is mostly precipitated on top of the original crack surface and may under certain circumstances fill the crack. The produced thin layers of low porosity calcite act as a diffusion barrier limiting contact between cement and solution. Pore closure mechanisms in such layers are discussed. Implications for safety assessment of radioactive waste disposal are shortly mentioned. The model is also relevant for conventional uses of concrete. (au)

  12. Inhibition of calcium carbonate deposition on stainless steel using olive leaf extract as a green inhibitor.

    Science.gov (United States)

    Aidoud, Roumaissa; Kahoul, Abdelkrim; Naamoune, Farid

    2017-01-01

    The antiscale properties of the aqueous extract of olive (Olea europaea L.) leaves as a natural scale inhibitor for stainless steel surface in Hammam raw water were investigated using chronoamperometry (CA) and electrochemical impedance spectroscopy techniques in conjunction with a microscopic examination. The X-ray diffraction analysis reveals that the scale deposited over the pipe walls consists of pure CaCO3 calcite. The CA, in accordance with electrochemical impedance spectra and scanning electron microscopy, shows that the inhibition efficiency increases with increasing extract concentration. This efficiency is considerably reduced as the temperature is increased.

  13. The cationic composition and pH in the moulting fluid of Porcellio scaber (Crustacea, Isopoda) during calcium carbonate deposit formation and resorption.

    Science.gov (United States)

    Ziegler, Andreas

    2008-01-01

    Before moulting, terrestrial isopods resorb calcium carbonate (CaCO(3)) from the posterior cuticle and store it in sternal deposits. These consist mainly of amorphous calcium carbonate (ACC) spherules that develop within the ecdysial space between the anterior sternal epithelium and the old cuticle. Ions that occur in the moulting fluid, including those required for mineral deposition, are transported from the hemolymph into the ecdysial space by the anterior sternal epithelial cells. The cationic composition of the moulting fluid probably affects mineral deposition and may provide information on the ion-transport activity of the sternal epithelial cells. This study presents the concentrations of inorganic cations within the moulting fluid of the anterior sternites during the late premoult and intramoult stages. The most abundant cation is Na(+) followed by Mg(2+), Ca(2+) and K(+). The concentrations of these ions do not change significantly between the stages whereas the mean pH changed from 8.2 to 6.9 units between mineral deposition in late premoult, and resorption in intramoult, respectively. Measurements of the transepithelial potential show that there is little driving force for passive movements of calcium across the anterior sternal epithelium. The results suggest a possible role of magnesium ions in ACC formation, and a contribution of pH changes to CaCO(3) precipitation and dissolution.

  14. Calcium carbonate overdose

    Science.gov (United States)

    Calcium carbonate is not very poisonous. Recovery is quite likely. But, long-term overuse is more serious than a single overdose, because it can cause kidney damage. Few people die from an antacid overdose. Keep all medicines in child-proof bottles and out ...

  15. Effect of Ultrasound on Calcium Carbonate Crystallization

    NARCIS (Netherlands)

    Wagterveld, R.M.

    2013-01-01

    Scaling comprises the formation of hard mineral deposits on process or membrane equipment and calcium carbonate is the most common scaling salt. Especially in reverse osmosis (RO) membrane systems, scale formation has always been a serious limitation, causing flux decline, membrane degradation, loss

  16. Real-time monitoring of calcium carbonate and cationic peptide deposition on carboxylate-SAM using a microfluidic SAW biosensor

    Directory of Open Access Journals (Sweden)

    Anna Pohl

    2014-10-01

    Full Text Available A microfluidic biosensor with surface acoustic wave technology was used in this study to monitor the interaction of calcium carbonate with standard carboxylate self-assembled monolayer sensor chips. Different fluids, with and without biomolecular components, were investigated. The pH-dependent surface interactions of two bio-inspired cationic peptides, AS8 and ES9, which are similar to an extracellular domain of the chitin synthase involved in mollusc shell formation, were also investigated in a biological buffer system. A range of experimental conditions are described that are suitable to study non-covalent molecular interactions in the presence of ionic substances, such as, mineral precursors below the solubility equilibrium. The peptide ES9, equal to the mollusc chitin synthase epitope, is less sensitive to changes in pH than its counterpart AS8 with a penta-lysine core, which lacks the flanking acidic residues. This study demonstrates the extraordinary potential of microfluidic surface acoustic wave biosensors to significantly expand our experimental capabilities for studying the principles underlying biomineralization in vitro.

  17. 21 CFR 184.1191 - Calcium carbonate.

    Science.gov (United States)

    2010-04-01

    ... HUMAN CONSUMPTION (CONTINUED) DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE Listing of... soda process”; (2) By precipitation of calcium carbonate from calcium hydroxide in the...

  18. 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)

  19. Calcium isotope constraints on the marine carbon cycle and CaCO3 deposition during the late Silurian (Ludfordian) positive δ13C excursion

    Science.gov (United States)

    Farkaš, Juraj; Frýda, Jiří; Holmden, Chris

    2016-10-01

    This study investigates calcium isotope variations (δ 44 / 40 Ca) in late Silurian marine carbonates deposited in the Prague Basin (Czech Republic), which records one of the largest positive carbon isotope excursion (CIE) of the entire Phanerozoic, the mid-Ludfordian CIE, which is associated with major climatic changes (abrupt cooling) and global sea-level fluctuations. Our results show that during the onset of the CIE, when δ13 C increases rapidly from ∼0‰ to ∼8.5‰, δ 44 / 40Ca remains constant at about 0.3 ± 0.1 ‰ (relative to NIST 915a), while 87Sr/86Sr in well-preserved carbonates are consistent with a typical Ludfordian seawater composition (ranging from ∼0.70865 to ∼0.70875). Such decoupling between δ13 C and δ 44 / 40Ca trends during the onset of the CIE is consistent with the expected order-of-magnitude difference in the residence times of Ca (∼106yr) and C (∼105yr) in the open ocean, suggesting that the mid-Ludfordian CIE was caused by processes where the biogeochemical pathways of C and Ca in seawater were mechanistically decoupled. These processes may include: (i) near shore methanogenesis and photosynthesis, (ii) changes in oceanic circulation and stratification, and/or (iii) increased production and burial of organic C in the global ocean. The latter, however, is unlikely due to the lack of geological evidence for enhanced organic C burial, and also because of unrealistic parameterization of the ocean C cycle needed to generate the observed CIE over the relatively short time interval. In contrast, higher up in the section where δ13 C shifts back to pre-excursion baseline values, there is a correlated shift to higher δ 44 / 40Ca values. Such coupling of the records of Ca and C isotope changes in this part of the study section is inconsistent with the abovementioned differences in oceanic Ca and C residence times, indicating that the record of δ 44 / 40Ca changes does not faithfully reflect the evolution of the oceanic Ca

  20. Variable efficacy of calcium carbonate tablets.

    Science.gov (United States)

    Kobrin, S M; Goldstein, S J; Shangraw, R F; Raja, R M

    1989-12-01

    Orally administered calcium carbonate tablets are commonly prescribed as a calcium supplement and for their phosphate-binding effects in renal failure patients. Two cases are reported in which a commercially available brand of calcium carbonate tablets appeared to be ineffective. Formal investigation of the bioavailability of this product revealed it to have impaired disintegration and dissolution and a lack of clinical efficacy. Recommendations that will enable physicians to avoid prescribing and pharmacists to avoid dispensing ineffective calcium carbonate tablets are proposed.

  1. Proliferation and differentiation of osteoblast-like MC3T3-E1 cells on biomimetically and electrolytically deposited calcium phosphate coatings

    NARCIS (Netherlands)

    Wang, Jiawei; Boer, de Jan; Groot, de Klaas

    2008-01-01

    Biomimetic and electrolytic deposition are versatile methods to prepare calcium phosphate coatings. In this article, we compared the effects of biomimetically deposited octacalcium phosphate and carbonate apatite coatings as well as electrolytically deposited carbonate apatite coating on the prolife

  2. Oral calcium carbonate affects calcium but not phosphorus balance in stage 3-4 chronic kidney disease.

    Science.gov (United States)

    Hill, Kathleen M; Martin, Berdine R; Wastney, Meryl E; McCabe, George P; Moe, Sharon M; Weaver, Connie M; Peacock, Munro

    2013-05-01

    Patients with chronic kidney disease (CKD) are given calcium carbonate to bind dietary phosphorus, reduce phosphorus retention, and prevent negative calcium balance; however, data are limited on calcium and phosphorus balance during CKD to support this. Here, we studied eight patients with stage 3 or 4 CKD (mean estimated glomerular filtration rate 36 ml/min) who received a controlled diet with or without a calcium carbonate supplement (1500 mg/day calcium) during two 3-week balance periods in a randomized placebo-controlled cross-over design. All feces and urine were collected during weeks 2 and 3 of each balance period and fasting blood, and urine was collected at baseline and at the end of each week. Calcium kinetics were determined using oral and intravenous (45)calcium. Patients were found to be in neutral calcium and phosphorus balance while on the placebo. Calcium carbonate supplementation produced positive calcium balance, did not affect phosphorus balance, and produced only a modest reduction in urine phosphorus excretion compared with placebo. Calcium kinetics demonstrated positive net bone balance but less than overall calcium balance, suggesting soft-tissue deposition. Fasting blood and urine biochemistries of calcium and phosphate homeostasis were unaffected by calcium carbonate. Thus, the positive calcium balance produced by calcium carbonate treatment within 3 weeks cautions against its use as a phosphate binder in patients with stage 3 or 4 CKD, if these findings can be extrapolated to long-term therapy.

  3. OSTEOPOROSIS IN CALCIUM PYROPHOSPHATE CRYSTAL DEPOSITION DISEASE

    Directory of Open Access Journals (Sweden)

    S A Vladimirov

    2013-01-01

    Full Text Available Objective: to study the incidence of osteoporosis (OP in patients with calcium pyrophosphate crystal deposition disease (CPCDD. Subjects and methods. Eighty patients with CPCDD were examined. Bone mineral density (BMD of the forearm, lumbar spine, and femoral neck was determined by dual-energy X-ray absorptiometry. Laboratory diagnosis involved determination of the blood levels of C-reactive protein, parathyroid hormone, calcium, magnesium, and phosphorus and the daily urinary excretion of calcium and phosphates. Results. The patients with OP were significantly older than those with normal BMD and osteopenia. Forearm bones were the most common isolated location of OP and osteopenia. Injuries in the history, traumatic fractures, and the intake of diuretics were somewhat more common in the patients diagnosed with OP. The incidence of hyperparathyroidism did not differ significantly in the groups.

  4. Elemental calcium intake associated with calcium acetate/calcium carbonate in the treatment of hyperphosphatemia

    OpenAIRE

    Wilson, Rosamund J; Copley, J Brian

    2017-01-01

    Background Calcium-based and non-calcium-based phosphate binders have similar efficacy in the treatment of hyperphosphatemia; however, calcium-based binders may be associated with hypercalcemia, vascular calcification, and adynamic bone disease. Scope A post hoc analysis was carried out of data from a 16-week, Phase IV study of patients with end-stage renal disease (ESRD) who switched to lanthanum carbonate monotherapy from baseline calcium acetate/calcium carbonate monotherapy. Of the intent...

  5. [Calcium suppletion for patients who use gastric acid inhibitors: calcium citrate or calcium carbonate?].

    NARCIS (Netherlands)

    Jonge, H.J. de; Gans, R.O.; Huls, G.A.

    2012-01-01

    Various calcium supplements are available for patients who have an indication for calcium suppletion. American guidelines and UpToDate recommend prescribing calcium citrate to patients who use antacids The rationale for this advice is that water-insoluble calcium carbonate needs acid for adequate ab

  6. Enzymatic pH control for biomimetic deposition of calcium phosphate coatings

    NARCIS (Netherlands)

    Nijhuis, A.W.G.; Nejadnik, M.R.; Nudelman, F.; Walboomers, X.F.; Riet, J. te; Habibovic, P.; Tahmasebi Birgani, Z.; Li, Y.; Bomans, P.H.; Jansen, J.A.; Sommerdijk, N.A.; Leeuwenburgh, S.C.G.

    2014-01-01

    The current study examines the enzymatic decomposition of urea into carbon dioxide and ammonia as a means to increase the pH during biomimetic deposition of calcium phosphate (CaP) onto implant surfaces. The kinetics of the enzymatically induced pH increase were studied by monitoring pH, calcium con

  7. Enzymatic pH Control for Biomimetic Deposition of Calcium Phosphate Coatings

    NARCIS (Netherlands)

    Nijhuis, A.W.; Reza Nejadnik, M.; Nudelman, F.; Walboomers, X.F.; Riet, te J.; Habibovic, P.; Tahmasebi Birgani, Z.; Yubao, L.; Bomans, P.H.H.; Jansen, J.A.; Sommerdijk, N.A.J.M.; Leeuwenburgh, S.C.G.

    2014-01-01

    The current study has focused on enzymatic decomposition of urea into carbon dioxide and ammonia as a means to increase the pH during biomimetic deposition of Calcium Phospate (CaP) onto implant surfaces. The kinetics of the enzymatically induced pH increase were studied by monitoring pH, calcium co

  8. Ultrasound influence upon calcium carbonate precipitation on bacterial cellulose membranes.

    Science.gov (United States)

    Stoica-Guzun, Anicuta; Stroescu, Marta; Jinga, Sorin; Jipa, Iuliana; Dobre, Tanase; Dobre, Loredana

    2012-07-01

    The effect of ultrasonic irradiation (40 kHz) on the calcium carbonate deposition on bacterial cellulose membranes was investigated using calcium chloride (CaCl(2)) and sodium carbonate (Na(2)CO(3)) as starting reactants. The composite materials containing bacterial cellulose-calcium carbonate were characterized by means of scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and color measurements. The polymorphs of calcium carbonate that were deposited on bacterial cellulose membranes in the presence or in the absence of ultrasonic irradiation were calcite and vaterite. The morphology of the obtained crystals was influenced by the concentration of starting solutions and by the presence of ultrasonic irradiation. In the presence of ultrasonic irradiation the obtained crystals were bigger and in a larger variety of shapes than in the absence of ultrasounds: from cubes of calcite to spherical and flower-like vaterite particles. Bacterial cellulose could be a good matrix for obtaining different types of calcium carbonate crystals.

  9. Calcium pyrophosphate deposition disease: clinical manifestations

    Directory of Open Access Journals (Sweden)

    M.A. Cimmino

    2012-01-01

    Full Text Available Calcium pyrophosphate deposition (CPPD disease is an arthropathy caused by calcium pyrophosphate dihydrate (CPP crystal deposits in articular tissues, most commonly fibrocartilage and hyaline cartilage. According to EULAR, four different clinical presentations can be observed: 1 asymptomatic CPPD; 2 osteoarthritis (OA with CPPD; 3 acute CPP crystal arthritis; 4 chronic CPP inflammatory crystal arthritis. Acute CPP crystal arthritis is characterized by sudden onset of pain, swelling and tenderness with overlying erythema, usually in a large joint, most often the knee, wrist, shoulder, and hip. Occasionally, ligaments, tendons, bursae, bone and the spine can be involved. CPPD of the atlanto-occipital joint (crowned dens syndrome can cause periodic acute cervico-occipital pain with fever, neck stiffness and laboratory inflammatory syndrome. Chronic inflammatory arthritis is characterized by joint swelling, morning stiffness, pain, and high ESR and CRP. The relationship between OA and CPPD is still unclear. The main problem is whether such crystals are directly involved in the pathogenesis of OA or if they are the result of joint degeneration. Diagnosis is based on evaluation of history and clinical features, conventional radiology, and synovial fluid examination. Non-polarized light microscopy should be used initially to screen for CPPD crystals based upon their characteristic morphology, and compensated polarized light microscopy, showing the crystals to be weakly positive birefringent, is recommended for definitive identification, although this last pattern only occurs in about 20% of samples. The main goals of CPPD therapy are control of the acute or chronic inflammatory reaction and prevention of further episodes.

  10. 碳酸钙在流动过冷沸腾条件下的结垢机理研究%Mechanism of Calcium Carbonate Scale Deposition under Subcooled Flow Boiling Conditions

    Institute of Scientific and Technical Information of China (English)

    邢晓凯; 马重芳; 陈永昌

    2005-01-01

    Fouling of heat transfer surfaces during subcooled flow boiling is a frequent engineering problem in process industries. It has been generally observed that the deposits in such industrial systems consist mainly of calcium carbonate (CaCO3), which has inverse solubility characteristics. This investigation focused on the mechanism to control deposition and the morphology of crystalline deposits. A series of experiments were carried out at different surface and bulk temperatures, fluid velocities and salt ion concentrations. It is shown that the deposition rate is controlled by different mechanism in the range of experimental parameters, depending on salt ion concentration. At higher ion concentration, the fouling rate increases linearly with surface temperature and the effect of flow velocity on deposition rate is quite strong, suggesting that mass diffusion controls the fouling process.On the contrary, at lower ion concentration, the fouling rate increases exponentially with surface temperature and is independent of the velocity, illustrating that surface reaction controls the fouling process. By analysis of the morphology of scale, two types of crystal (calcite and aragonite) are formed. The lower the temperature and ion concentration, the longer the induction period and the higher the percentage of calcite precipitated.

  11. The Blue-green Algae Calcification Test Preliminary Research on Land Facies Calcium Carbonate Deposit in Different Water Hydrodynamic Condition%不同水动力下陆相碳酸钙沉积的蓝藻钙化试验的初步研究

    Institute of Scientific and Technical Information of China (English)

    程星; 石方红; 李本刚; 张金梅; 潘响亮

    2012-01-01

    The surface calcification is a kind of deposit on the earth, which is an important deposit type of land calci- um carbonate. For a long time, the hydrodynamic formation cause of land calcium carbonate deposit is familiar to the researchers. The research of the biological cause of the formation is relatively fewer. In fact, the biological cause should be not ignored as well, especially algous deposit process. From imitating for field hydrodynamic force condi- tion, taking the blue-green algae for example, the research makes a biological deposit test under the different hydrody- namic force condition. From the test, we get optimum hydrodynamic condition of algae growth and their calcification rate, that is under the rate of 0 ~ 60 rpm, under the excessive strong , the growth of blue-green algae will be restrain- ed, and reduce the deposit rate of calcium carbonate. Under the condition of waterfall, hydrodynamic force is strong, in calcium carbonate depositing process, hydrodynamic formation cause of land calcium carbonate deposit is the lead cause; Under the weaker hydrodynamic condition, such as in fiver bed, biological calcification deposit will be the lead cause. Therefore, hydrodynamic-biological cause viewpoint has been proposed in the article. From the field algous samples, the calcium carbonate depositing test has been done under the different water hy- drodynamic conditions. The test results show that under the faster water condition, most calcium carbonate will deposit very quick, and fewer algae calcium carbonate will precipitate because of adverse living environment under the condi- tion. And under the slower water condition, because of being avail for algae' s living, more algae calcium carbonate will precipitate, and few calcium carbonate will deposit under the condition without algae. Also, under the motionless condition, contribution of calcium carbonate deposit have been compared in the article between the algous environment and without algous

  12. Morphological Investigation of Calcium Carbonate during Ammonification-Carbonization Process of Low Concentration Calcium Solution

    Directory of Open Access Journals (Sweden)

    Huaigang Cheng

    2014-01-01

    Full Text Available Ultrafine calcium carbonate is a widely used cheap additive. The research is conducted in low degree supersaturation solution in order to study the polymorphic phases’ change and its factors of the calcium carbonate precipitate in the ammonification-carbonization process of the solution with calcium. Fine particles of calcium carbonate are made in the solution containing 0.015 mol/L of Ca2+. Over 98% of the calcium carbonate precipitate without ammonification resembles the morphology of calcite, while the introduction of ammonia can benefit the formation of vaterite. It was inferred that the main cause should be serious partial oversaturation or steric effects. Ammonia also helps to form the twin spherical calcium carbonate. However, particles formed in the process of ammonification-carbonization in solution with low concentration degree of calcium are not even with a scale of the particle diameter from 5 to 12 μm. Inorganic salts, alcohol, or organic acid salts have significant controlling effect on the particle diameter of calcium carbonate and can help to decrease the particle diameter to about 3 μm. Anionic surfactants can prevent the conglobation of calcium carbonate particles and shrink its diameter to 500 nm–1 μm.

  13. Elemental calcium intake associated with calcium acetate/calcium carbonate in the treatment of hyperphosphatemia

    Science.gov (United States)

    Wilson, Rosamund J; Copley, J Brian

    2017-01-01

    Background Calcium-based and non-calcium-based phosphate binders have similar efficacy in the treatment of hyperphosphatemia; however, calcium-based binders may be associated with hypercalcemia, vascular calcification, and adynamic bone disease. Scope A post hoc analysis was carried out of data from a 16-week, Phase IV study of patients with end-stage renal disease (ESRD) who switched to lanthanum carbonate monotherapy from baseline calcium acetate/calcium carbonate monotherapy. Of the intent-to-treat population (N=2520), 752 patients with recorded dose data for calcium acetate (n=551)/calcium carbonate (n=201) at baseline and lanthanum carbonate at week 16 were studied. Elemental calcium intake, serum phosphate, corrected serum calcium, and serum intact parathyroid hormone levels were analyzed. Findings Of the 551 patients with calcium acetate dose data, 271 (49.2%) had an elemental calcium intake of at least 1.5 g/day at baseline, and 142 (25.8%) had an intake of at least 2.0 g/day. Mean (95% confidence interval [CI]) serum phosphate levels were 6.1 (5.89, 6.21) mg/dL at baseline and 6.2 (6.04, 6.38) mg/dL at 16 weeks; mean (95% CI) corrected serum calcium levels were 9.3 (9.16, 9.44) mg/dL and 9.2 (9.06, 9.34) mg/dL, respectively. Of the 201 patients with calcium carbonate dose data, 117 (58.2%) had an elemental calcium intake of at least 1.5 g/day, and 76 (37.8%) had an intake of at least 2.0 g/day. Mean (95% CI) serum phosphate levels were 5.8 (5.52, 6.06) mg/dL at baseline and 5.8 (5.53, 6.05) mg/dL at week 16; mean (95% CI) corrected serum calcium levels were 9.7 (9.15, 10.25) mg/dL and 9.2 (9.06, 9.34) mg/dL, respectively. Conclusion Calcium acetate/calcium carbonate phosphate binders, taken to control serum phosphate levels, may result in high levels of elemental calcium intake. This may lead to complications related to calcium balance. PMID:28182142

  14. Evaluation of quick disintegrating calcium carbonate tablets

    OpenAIRE

    Fausett, Hector; Gayser, Charles; Dash, Alekha K.

    2000-01-01

    The purpose of this investigation was to develop a rapidly disintegrating calcium carbonate (CC) tablet by direct compression and compare it with commercially available calcium tablets. CC tablets were formulated on a Carver press using 3 different forms of CC direct compressed granules (Cal-Carb 4450®, Cal-Carb 4457®, and Cal-Carb 4462®). The breaking strength was measured using a Stokes-Monsanto hardness tester. The disintegration and dissolution properties of the tablets were studied using...

  15. Divalent Mn in calcium hydroxyapatite by pulse laser deposition.

    Science.gov (United States)

    Mayer, I; Peto, G; Karacs, A; Molnár, G; Popov, I

    2010-10-01

    Pulse laser deposition (PLD) was used to deposit Mn containing calcium hydroxyapatite (HAMn). The PLD process ensures that the composition of the target and the deposited layer is the same. In some cases additional effort should be made to preserve some volatile components, namely OH. This was ensured by water steam supply. Calcium hydroxyapatite deposited by this method has the same properties as the target in respect to lattice parameters and valence state of Mn, which ensures the fixation between hard tissue and metal implants. This fact makes PLD grown HAMn layer covering implants to be improved for practical use.

  16. Diagnosis and clinical manifestations of calcium pyrophosphate and basic calcium phosphate crystal deposition diseases.

    Science.gov (United States)

    Ea, Hang-Korng; Lioté, Frédéric

    2014-05-01

    Basic calcium phosphate and pyrophosphate calcium crystals are the 2 main calcium-containing crystals that can deposit in all skeletal tissues. These calcium crystals give rise to numerous manifestations, including acute inflammatory attacks that can mimic alarming and threatening differential diagnoses, osteoarthritis-like lesions, destructive arthropathies, and calcific tendinitis. Awareness of uncommon localizations and manifestations such as intraspinal deposition (eg, crowned dens syndrome, tendinitis of longus colli muscle, massive cervical myelopathy compression) prevents inappropriate procedures and cares. Coupling plain radiography, ultrasonography, computed tomography, and synovial fluid analysis allow accurate diagnosis by directly or indirectly identifying the GRAAL of microcrystal-related symptoms.

  17. Absence of rebound effect with calcium carbonate.

    Science.gov (United States)

    Simoneau, G

    1996-01-01

    This was an open, randomised balance cross-over study in 12 healthy male volunteers. The antacid activity of calcium carbonate plus magnesium carbonate (Rennie and hydrotalcite (Talcid), given in the recommended dose of 2 tablets 4 times daily, were compared using 24 h intragastric measurement of pH. The volunteers received 2 tablets of calcium carbonate plus magnesium carbonate or hydrotalcite according to a randomised order 1 h after each meal and at bedtime. Results showed that both treatments have similar antacid efficacy and a similar duration of action of about one hour. There was no evidence of acid 'rebound' following either treatment during the second and third hours following the administration of antacid.

  18. The Thermal Decomposition of Calcium Carbonate

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The thermogravimetry(TG) and derivative thermogravimetry(DTG) curves of the thermal decomposition reaction of calcium carbonate have been measured at five different heating rates. The kinetic parameters and the reaction mechanism of the reaction were evaluated from analysis of the TG and DTG curves by using the Ozawa method, the combined integral and differential methods and the reduced equations derived by us.

  19. Fibroblast-like synoviocytes induce calcium mineral formation and deposition.

    Science.gov (United States)

    Sun, Yubo; Mauerhan, David R; Franklin, Atiya M; Zinchenko, Natalia; Norton, Harry James; Hanley, Edward N; Gruber, Helen E

    2014-01-01

    Calcium crystals are present in the synovial fluid of 65%-100% patients with osteoarthritis (OA) and 20%-39% patients with rheumatoid arthritis (RA). This study sought to investigate the role of fibroblast-like synoviocytes (FLSs) in calcium mineral formation. We found that numerous genes classified in the biomineral formation process, including bone gamma-carboxyglutamate (gla) protein/osteocalcin, runt-related transcription factor 2, ankylosis progressive homolog, and parathyroid hormone-like hormone, were differentially expressed in the OA and RA FLSs. Calcium deposits were detected in FLSs cultured in regular medium in the presence of ATP and FLSs cultured in chondrogenesis medium in the absence of ATP. More calcium minerals were deposited in the cultures of OA FLSs than in the cultures of RA FLSs. Examination of the micromass stained with nonaqueous alcoholic eosin indicated the presence of birefringent crystals. Phosphocitrate inhibited the OA FLSs-mediated calcium mineral deposition. These findings together suggest that OA FLSs are not passive bystanders but are active players in the pathological calcification process occurring in OA and that potential calcification stimuli for OA FLSs-mediated calcium deposition include ATP and certain unidentified differentiation-inducing factor(s). The OA FLSs-mediated pathological calcification process is a valid target for the development of disease-modifying drug for OA therapy.

  20. Fibroblast-Like Synoviocytes Induce Calcium Mineral Formation and Deposition

    Directory of Open Access Journals (Sweden)

    Yubo Sun

    2014-01-01

    Full Text Available Calcium crystals are present in the synovial fluid of 65%–100% patients with osteoarthritis (OA and 20%–39% patients with rheumatoid arthritis (RA. This study sought to investigate the role of fibroblast-like synoviocytes (FLSs in calcium mineral formation. We found that numerous genes classified in the biomineral formation process, including bone gamma-carboxyglutamate (gla protein/osteocalcin, runt-related transcription factor 2, ankylosis progressive homolog, and parathyroid hormone-like hormone, were differentially expressed in the OA and RA FLSs. Calcium deposits were detected in FLSs cultured in regular medium in the presence of ATP and FLSs cultured in chondrogenesis medium in the absence of ATP. More calcium minerals were deposited in the cultures of OA FLSs than in the cultures of RA FLSs. Examination of the micromass stained with nonaqueous alcoholic eosin indicated the presence of birefringent crystals. Phosphocitrate inhibited the OA FLSs-mediated calcium mineral deposition. These findings together suggest that OA FLSs are not passive bystanders but are active players in the pathological calcification process occurring in OA and that potential calcification stimuli for OA FLSs-mediated calcium deposition include ATP and certain unidentified differentiation-inducing factor(s. The OA FLSs-mediated pathological calcification process is a valid target for the development of disease-modifying drug for OA therapy.

  1. Preparation and Characterization of Calcium Carbonate Nanoparticles

    Science.gov (United States)

    Hassim, Aqilah; Rachmawati, Heni

    2010-10-01

    Taking calcium supplements can reduce the risk of developing osteoporosis, but they are not readily absorbed in the gastrointestinal tract. Nanotechnology is expected to resolve this problem. In this study, we prepared and characterized calcium carbonate nanoparticle to improve the solubility by using bottom-up method. The experiment was done by titrating calcium chloride with sodium carbonate with the addition of polyvinylpyrrolidone (PVP) as stabilizer, using ultra-turrax. Various concentrations of calcium chloride and sodium carbonate as well as various speed of stirring were used to prepare the calcium carbonate nanoparticles. Evaluations studied were including particle size, polydispersity index (PI) and zeta potential with particle analyzer, surface morphology with scanning electron microscope, and saturated solubility. In addition, to test the ability of PVP to prevent particles growth, short stability study was performed by storing nano CaCO3 suspension at room temperature for 2 weeks. Results show that using 8000 rpm speed of stirring, the particle size tends to be bigger with the range of 500-600 nm (PI between 0.2-0.4) whereas with stirring speed of 4000 rpm, the particle size tends to be smaller with 300-400 nm (PI between 0.2-0.4). Stirring speed of 6000 rpm produced particle size within the range of 400-500 nm (PI between 0.2-0.4). SEM photograph shows that particles are monodisperse confirming that particles were physically stable without any agglomeration within 2 weeks storage. Taken together, nano CaCO3 is successfully prepared by bottom-up method and PVP is a good stabilizer to prevent the particle growth.

  2. Role of magnesium on the biomimetic deposition of calcium phosphate

    Science.gov (United States)

    Sarma, Bimal K.; Sarma, Bikash

    2016-10-01

    Biomimetic depositions of calcium phosphate (CaP) are carried out using simulated body fluid (SBF), calcifying solution and newly developed magnesium containing calcifying solution. Calcium phosphate has a rich phase diagram and is well known for its excellent biocompatibility and bioactivity. The most common phase is hydroxyapatite (HAp), an integral component of human bone and tooth, widely used in orthopedic and dental applications. In addition, calcium phosphate nanoparticles show promise for the targeted drug delivery. The doping of calcium phosphate by magnesium, zinc, strontium etc. can change the protein uptake by CaP nanocrystals. This work describes the role of magnesium on the nucleation and growth of CaP on Ti and its oxide substrates. X-ray diffraction studies confirm formation of HAp nanocrystals which closely resemble the structure of bone apatite when grown using SBF and calcifying solution. It has been observed that magnesium plays crucial role in the nucleation and growth of calcium phosphate. A low magnesium level enhances the crystallinity of HAp while higher magnesium content leads to the formation of amorphous calcium phosphate (ACP) phase. Interestingly, the deposition of ACP phase is rapid when magnesium ion concentration in the solution is 40% of calcium plus magnesium ions concentration. Moreover, high magnesium content alters the morphology of CaP films.

  3. Evaluation of quick disintegrating calcium carbonate tablets.

    Science.gov (United States)

    Fausett, H; Gayser, C; Dash, A K

    2000-07-02

    The purpose of this investigation was to develop a rapidly disintegrating calcium carbonate (CC) tablet by direct compression and compare it with commercially available calcium tablets. CC tablets were formulated on a Carver press using 3 different forms of CC direct compressed granules (Cal-Carb 4450, Cal-Carb 4457, and Cal-Carb 4462). The breaking strength was measured using a Stokes-Monsanto hardness tester. The disintegration and dissolution properties of the tablets were studied using USP methodology. The calcium concentration was determined by an atomic absorption spectrophotometer. Scanning electron microscopy was used to evaluate the surface topography of the granules and tablets. Breaking strength of Cal-Carb 4450, Cal-Carb 4457, and Cal-Carb 4462 tablets was in the range of 7.2 to 7.7 kg, as compared with a hardness of 6.2 kg and 10 kg for the commercially available calcium tablets Citracal and Tums, respectively. The disintegration time for the tablets presented in the order earlier was 4.1, 2.1, 1.9, 2.9, and 9.7 minutes, respectively. The dissolution studies showed that all formulations released 100% of the elemental calcium in simulated gastric fluid in less than 20 minutes. In summary, this study clearly demonstrated that quick disintegrating CC tablets can be formulated without expensive effervescence technology.

  4. Multi-Functions of Carbonated Calcium Deficient Hydroxyapatite (CDHA)

    Science.gov (United States)

    Zhou, Huan

    Natural bone is a complex composite mainly constituted of inorganic minerals and organic collagen molecules. Calcium phosphate (CaP) based materials have been proposed as the predominant bone substitute for bone tissue engineering applications due to their chemical similarity to bone mineral. Amorphous carbonated calcium deficient hydroxyapatite (CDHA) is an important compound among CaP materials because of the amorphous crystallite structure. The presence of extra ions in its lattice structure not only influences cell attachment and proliferation of osteoblasts, but also helps in bone metabolism. Biomimetic coating approach is the most widely used approach to produce CDHA coatings to implant. It is a process using simulated body fluid (SBF) to deposit bone-like CDHA coating to various material surfaces. The CDHA formation mechanism, SBF compositions and reacting conditions of biomimetic coating have already been sufficiently studied and compared in the past 20 years. It is an attempt in this thesis to explore new applications of SBF in biomedical research, focusing on different biomaterial applications: 1) based on the low temperature reaction condition of SBF, bisphosphonate incorporated CDHA coatings were deposited onto Ti6Al4V surface for the treatment of osteoporosis; 2) amorphous calcium phosphate nanospheres with extra elements in the lattice structure were prepared by a novel microwave assisted approach, providing a new potential of CaP materials production; 3) CDHA particles formed in SBF can be used as great fillers with biopolymers for preparing biocomposites for biomedical applications; 4) based on the high activity of CDHA amorphous structure and the stabilization ability of ethanol, yttrium and europium doped calcium phosphates were prepared using CDHA as a sacrificing template. In the end, future work based on these observations in the thesis is addressed, including areas of drug delivery, biocomposite fabrication and preparation of functionalized

  5. Apatite Formation from Amorphous Calcium Phosphate and Mixed Amorphous Calcium Phosphate/Amorphous Calcium Carbonate.

    Science.gov (United States)

    Ibsen, Casper J S; Chernyshov, Dmitry; Birkedal, Henrik

    2016-08-22

    Crystallization from amorphous phases is an emerging pathway for making advanced materials. Biology has made use of amorphous precursor phases for eons and used them to produce structures with remarkable properties. Herein, we show how the design of the amorphous phase greatly influences the nanocrystals formed therefrom. We investigate the transformation of mixed amorphous calcium phosphate/amorphous calcium carbonate phases into bone-like nanocrystalline apatite using in situ synchrotron X-ray diffraction and IR spectroscopy. The speciation of phosphate was controlled by pH to favor HPO4 (2-) . In a carbonate free system, the reaction produces anisotropic apatite crystallites with large aspect ratios. The first formed crystallites are highly calcium deficient and hydrogen phosphate rich, consistent with thin octacalcium phosphate (OCP)-like needles. During growth, the crystallites become increasingly stoichiometric, which indicates that the crystallites grow through addition of near-stoichiometric apatite to the OCP-like initial crystals through a process that involves either crystallite fusion/aggregation or Ostwald ripening. The mixed amorphous phases were found to be more stable against phase transformations, hence, the crystallization was inhibited. The resulting crystallites were smaller and less anisotropic. This is rationalized by the idea that a local phosphate-depletion zone formed around the growing crystal until it was surrounded by amorphous calcium carbonate, which stopped the crystallization.

  6. Comparative absorption of calcium from carbonate tablets, lactogluconate/carbonate effervescent tablet, and chloride solution.

    Science.gov (United States)

    Ekman, M; Reizenstein, P; Teigen, S W; Rønneberg, R

    1991-01-01

    Intestinal absorption of calcium from three different labelled calcium preparations (all containing 500 mg elemental calcium) was determined using the whole body retention and urinary excretion of 47Ca in 14 normal subjects. Chewable calcium carbonate tablets showed a significantly (p less than 0.05) better mean minimum absorption of calcium (25.6% in exp. I, 22.8% in exp. II) than calcium given in the form of a lactogluconate/carbonate effervescent tablet, (17%), but similar to calcium in a chloride solution (24.7%). The minimum calcium absorption varied from 85 to 128 mg. All the preparations were taken with standardized low calcium test meals.

  7. Calcium and calcium isotope changes during carbon cycle perturbations at the end-Permian

    Science.gov (United States)

    Komar, Nemanja; Zeebe, Richard

    2016-04-01

    Negative carbon and calcium isotope excursions, as well as climate shifts, took place during the most severe mass extinction event in Earth's history, the end-Permian (˜252 Ma). Investigating the connection between carbon and calcium cycles during transient carbon cycle perturbation events, such as the end-Permian, may help resolve the intricacies between the coupled calcium-carbon cycles, as well as provide a tool for constraining the causes of mass extinction. Here, we identify the deficiencies of a simplified calcium model employed in several previous studies and we demonstrate the importance of a fully coupled carbon-cycle model when investigating the dynamics of carbon and calcium cycling. Simulations with a modified version of the LOSCAR model, which includes a fully coupled carbon-calcium cycle, indicate that increased weathering rates and ocean acidification (potentially caused by Siberian Trap volcanism) are not capable of producing trends observed in the record, as previously claimed. Our model results suggest that combined effects of carbon input via Siberian Trap volcanism (12,000 Pg C), the cessation of biological carbon export, and variable calcium isotope fractionation (due to a change in the seawater carbonate ion concentration) represents a more plausible scenario. This scenario successfully reconciles δ13C and δ44Ca trends observed in the sediment record, as well as the proposed warming of >6oC.

  8. [Formulation of calcium carbonate tablets with various binding substances].

    Science.gov (United States)

    Gazikalović, E; Obrenović, D; Nidzović, Z; Toskić-Radojicić, M

    1996-01-01

    The test results of calcium carbonate tablets, made of different binding substances (microcrystal cellulose, gelatin, 7pp sodium carboxymethylcellulose and starch) were presented. The content of calcium-carbonate in tablets as well as varying, solidity, prodigality and aptness to decay was determined. The best properties were observed in tablets made with starch.

  9. A Brief Review on Calcium Pyrophosphate Deposition Disease (Pseudogout

    Directory of Open Access Journals (Sweden)

    Manoj A. Suva

    2014-08-01

    Full Text Available Calcium pyrophosphate deposition disease (CPDD or pseudo gout is a metabolic arthropathy caused by the deposition of calcium pyrophosphate dihydrate in and around joints especially in articular cartilage and fibro cartilage. Pseudo gout is a joint disease that can cause attacks of arthritis. Like gout, the condition involves the formation of crystals in the joints. But in pseudo gout, the crystals are formed from a salt instead of uric acid. Almost any joint may be involved by CPDD, although the knees, wrists, and hips are most often affected. Exact mechanism for the development of CPDD is still not known, but increased adenosine triphosphate breakdown which leads to increased inorganic pyrophosphate in the joints results from aging, genetic factors, or both. CPDD is a common condition that occurs with aging in all races. About 50% of people above 85 years have chondrocalcinosis in the United States. Physical examination findings show an acutely inflamed joint with swelling, effusion, warmth, tenderness and pain on motion similar to acute gouty arthritis and occur in the knee but may be present in the wrists, shoulders, ankles, hands and feet. Laboratory tests include serum calcium, phosphorus and magnesium, alkaline phosphatase levels, iron levels, total iron binding capacity, transferrin saturation and ferritin, thyroid-stimulating hormone and free thyroxine levels. Imaging studies like radiography, magnetic resonance imaging (MRI and Ultrasonography is done. Management of CPPD includes surgery and pharmacotherapy with Nonsteroidal anti-inflammatory drugs (NSAIDs, anti-inflammatory agents like colchicine and corticosteroids such as prednisone and methylprednisolone.

  10. Atomic structure of intracellular amorphous calcium phosphate deposits.

    Science.gov (United States)

    Betts, F; Blumenthal, N C; Posner, A S; Becker, G L; Lehninger, A L

    1975-06-01

    The radial distribution function calculated from x-ray diffraction of mineralized cytoplasmic structures isolated from the hepatopancreas of the blue crab (Callinectes sapidus) is very similar to that previously found for synthetic amorphous calcium phosphate. Both types of mineral apparently have only short-range atomic order, represented as a neutral ion cluster of about 10 A in longest dimension, whose probable composition is expressed by the formula Ca9(PO4)6. The minor differences observed are attributed to the presence in the biological mineral of significant amounts of Mg-2+ and ATP. Synthetic amorphous calcium phosphate in contact with a solution containing an amount of ATP equivalent to that of the biological mineral failed to undergo conversion to the thermodynamically more stable hydroxyapatite. The amorphous calcium phosphate of the cytoplasmic mineral granules is similarly stable, and does not undergo conversion to hydroxyapatite, presumably owing to the presence of ATP and Mg-2+, known in inhibitors of the conversion process. The physiological implications of mineral deposits consisting of stabilized calcium phosphate ion clusters are discussed.

  11. The skeletal organic matrix from Mediterranean coral Balanophyllia europaea influences calcium carbonate precipitation.

    Directory of Open Access Journals (Sweden)

    Stefano Goffredo

    Full Text Available Scleractinian coral skeletons are made mainly of calcium carbonate in the form of aragonite. The mineral deposition occurs in a biological confined environment, but it is still a theme of discussion to what extent the calcification occurs under biological or environmental control. Hence, the shape, size and organization of skeletal crystals from the cellular level through the colony architecture, were attributed to factors as diverse as mineral supersaturation levels and organic mediation of crystal growth. The skeleton contains an intra-skeletal organic matrix (OM of which only the water soluble component was chemically and physically characterized. In this work that OM from the skeleton of the Balanophyllia europaea, a solitary scleractinian coral endemic to the Mediterranean Sea, is studied in vitro with the aim of understanding its role in the mineralization of calcium carbonate. Mineralization of calcium carbonate was conducted by overgrowth experiments on coral skeleton and in calcium chloride solutions containing different ratios of water soluble and/or insoluble OM and of magnesium ions. The precipitates were characterized by diffractometric, spectroscopic and microscopic techniques. The results showed that both soluble and insoluble OM components influence calcium carbonate precipitation and that the effect is enhanced by their co-presence. The role of magnesium ions is also affected by the presence of the OM components. Thus, in vitro, OM influences calcium carbonate crystal morphology, aggregation and polymorphism as a function of its composition and of the content of magnesium ions in the precipitation media. This research, although does not resolve the controversy between environmental or biological control on the deposition of calcium carbonate in corals, sheds a light on the role of OM, which appears mediated by the presence of magnesium ions.

  12. Coating of calcium phosphate on biometallic materials by electrophoretic deposition

    Institute of Scientific and Technical Information of China (English)

    ZHANG Er-lin; YANG Ke

    2005-01-01

    Although biometallic materials have been used as bone implant materials for a long time, they are still detected as foreign bodies by human immune system. Calcium phosphate coating, especially hydroxyapatite(HA)coating attracts special attention due to its good biocompatibility. Being one of the effective methods used to deposit HA coating onto the metallic implant, the electrophoretic deposition(EPD) was reviewed in detail, including the process of EPD, the advantages and disadvantages, the important processing factors and the microstructure and mechanical properties of the coating. Research results on the processing and the coating show potential application of EPD process to the biomedical materials surface modification. In addition, the nanoparticulate HA coating as a new trend in HA coating was also introduced.

  13. Increased calcium absorption from synthetic stable amorphous calcium carbonate: Double-blind randomized crossover clinical trial in post-menopausal women

    Science.gov (United States)

    Calcium supplementation is a widely recognized strategy for achieving adequate calcium intake. We designed this blinded, randomized, crossover interventional trial to compare the bioavailability of a new stable synthetic amorphous calcium carbonate (ACC) with that of crystalline calcium carbonate (C...

  14. SECONDARY HYPERPARATHYROIDISM AFTER BARIATRIC SURGERY: TREATMENT IS WITH CALCIUM CARBONATE OR CALCIUM CITRATE?

    Science.gov (United States)

    BARETTA, Giorgio Alfredo Pedroso; CAMBI, Maria Paula Carlini; RODRIGUES, Arieli Luz; MENDES, Silvana Aparecida

    2015-01-01

    Background : Bariatric surgery, especially Roux-en-Y gastric bypass, can cause serious nutritional complications arising from poor absorption of essential nutrients. Secondary hyperparathyroidism is one such complications that leads to increased parathyroid hormone levels due to a decrease in calcium and vitamin D, which may compromise bone health. Aim : To compare calcium carbonate and calcium citrate in the treatment of secondary hyperparathyroidism. Method : Patients were selected on the basis of their abnormal biochemical test and treatment was randomly done with citrate or calcium carbonate. Results : After 60 days of supplementation, biochemical tests were repeated, showing improvement in both groups. Conclusion : Supplementation with calcium (citrate or carbonate) and vitamin D is recommended after surgery for prevention of secondary hyperparathyroidism. PMID:26537273

  15. Urea hydrolysis and calcium carbonate reaction fronts

    Science.gov (United States)

    Fox, D. T.; Redden, G. D.; Henriksen, J.; Fujita, Y.; Guo, L.; Huang, H.

    2010-12-01

    The mobility of toxic or radioactive metal contaminants in subsurface environments can be reduced by the formation of mineral precipitates that form co-precipitates with the contaminants or that isolate them from the mobile fluid phase. An engineering challenge is to control the spatial distribution of precipitation reactions with respect to: 1) the location of a contaminant, and 2) where reactants are introduced into the subsurface. One strategy being explored for immobilizing contaminants, such as Sr-90, involves stimulating mineral precipitation by forming carbonate ions and hydroxide via the in situ, microbially mediated hydrolysis of urea. A series of column experiments have been conducted to explore how the construction or design of such an in situ reactant production strategy can affect the temporal and spatial distribution of calcium carbonate precipitation, and how the distribution is coupled to changes in permeability. The columns were constructed with silica gel as the porous media. An interval midway through the column contained an adsorbed urease enzyme in order to simulate a biologically active zone. A series of influent solutions were injected to characterize hydraulic properties of the column (e.g., bromide tracer), profiles of chemical conditions and reaction products as the enzyme catalyzes urea hydrolysis (e.g., pH, ammonia, urea), and changes that occur due to CaCO3 precipitation with the introduction of a calcium+urea solutions. In one experiment, hydraulic conductivity was reduced as precipitate accumulated in a layer within the column that had a higher fraction of fine grained silica gel. Subsequent reduction of permeability and flow (for a constant head condition) resulted in displacement of the hydrolysis and precipitation reaction profiles upstream. In another experiment, which lacked the physical heterogeneity (fine grained layer), the precipitation reaction did not result in loss of permeability or flow velocity and the reaction profile

  16. Behaviour of calcium carbonate in sea water

    Science.gov (United States)

    Cloud, P.E.

    1962-01-01

    Anomalies in the behaviour of calcium carbonate in natural solutions diminish when considered in context. Best values found by traditional oceanographie methods for the apparent solubility product constant K'CaCO3 in sea water at atmospheric pressure are consistent mineralogically-at 36 parts per thousand salinity and T-25??C, K'aragonlte is estimated as 1.12 ?? 10-6 and K'calcite as 0.61 ?? 10-6. At 30??C the corresponding values are 0.98 ?? 10-6 for aragonite and 0.53 ?? 10-6 for calcite. Because the K' computations do not compensate for ionic activity, however, they cannot give thermodynamically satisfactory results. It is of interest, therefore, that approximate methods and information now available permit the estimation from the same basic data of an activity product constant KCaCO3 close to that found in solutions to which Debye-Hu??ckel theory applies. Such methods indicate approximate Karagonite 7.8 ?? 10-9 for surface sea water at 29??C; Kcalcite would be proportionately lower. Field data and experimental results indicate that the mineralogy of precipitated CaCO3 depends primarily on degree of supersaturation, thus also on kinetic or biologic factors that facilitate or inhibit a high degree of supersaturation. The shallow, generally hypersaline bank waters west of Andros Island yield aragonitic sediments with O18 O16 ratios that imply precipitation mainly during the warmer months, when the combination of a high rate of evaporation, increasing salinity (and ionic strength), maximal temperatures and photosynthetic removal of CO2 result in high apparent supersaturation. The usual precipitate from solutions of low ionic strength is calcite, except where the aragonite level of supersaturation is reached as a result of diffusion phenomena (e.g. dripstones), gradual and marked evaporation, or biologic intervention. Published data also suggest the possibility of distinct chemical milieus for crystallographic variations in skeletal calcium carbonate. It appears

  17. Synthesis of calcium hydroxyapatite from calcium carbonate and different orthophosphate sources: A comparative study

    Energy Technology Data Exchange (ETDEWEB)

    Pham Minh, Doan, E-mail: doan.phamminh@mines-albi.fr [Universite de Toulouse, Mines Albi, CNRS, Centre RAPSODEE, Campus Jarlard, F-81013 Albi cedex 09 (France); Lyczko, Nathalie; Sebei, Haroun; Nzihou, Ange [Universite de Toulouse, Mines Albi, CNRS, Centre RAPSODEE, Campus Jarlard, F-81013 Albi cedex 09 (France); Sharrock, Patrick [Universite de Toulouse, SIMAD, IUT Paul Sabatier, Avenue Georges Pompidou, 81104 Castres (France)

    2012-08-01

    Highlights: Black-Right-Pointing-Pointer Calcium hydroxyapatite was synthesized from CaCO{sub 3} and four orthophosphates. Black-Right-Pointing-Pointer Only H{sub 3}PO{sub 4} led to the complete precipitation of orthophosphate species. Black-Right-Pointing-Pointer H{sub 3}PO{sub 4} was also the most efficient for calcium dissolution. Black-Right-Pointing-Pointer Reaction pathway was dissolution-precipitation accompanied by agglomeration step. - Abstract: The synthesis of calcium hydroxyapatite (Ca-HA) starting from calcium carbonate and different orthophosphate sources, including orthophosphoric acid, potassium, sodium and ammonium dihydrogen orthophosphates, was investigated under ambient conditions. The reaction started with calcium carbonate dissolution in an acid medium, followed by rapid precipitation of calcium cations with orthophosphate species to form calcium phosphate based particles which were in the size range of 0.4-1 {mu}m. These particles then agglomerated into much larger ones, up to 350 {mu}m in diameter (aggregates). These aggregates possessed an unstable porous structure which was responsible for the porosity of the final products. The highest specific surface area and pore volume were obtained with potassium dihydrogen orthophosphate. On the other hand, orthophosphoric acid led to the highest dissolution of calcium carbonate and the complete precipitation of orthophosphate species. Under ambient conditions, calcium phosphate based solid products of low crystallinity were formed. Different intermediates were identified and a reaction pathway proposed.

  18. Fortification of all-purpose wheat-flour tortillas with calcium lactate, calcium carbonate, or calcium citrate is acceptable.

    Science.gov (United States)

    Romanchik-Cerpovicz, Joelle E; McKemie, Rebecca J

    2007-03-01

    Fortification helps provide adequate nutrients for individuals not meeting daily needs. Foods may be fortified with calcium to assist individuals with lactose intolerance and others preferring not to consume traditional forms of dairy. This study examined the quality of all-purpose wheat-flour tortillas fortified with calcium lactate, calcium carbonate, or calcium citrate. These tortillas were compared to similarly prepared nonfortified flour tortillas (control) and commercial nonfortified flour tortillas. Calcium-fortified tortillas contained 114 mg elemental calcium per standard serving (48 g tortilla), an 8.6-fold increase compared to nonfortified tortillas. Moisture contents and rollabilities of all tortillas were similar. Consumers (N=87) evaluated each tortilla in duplicate using a hedonic scale and reported liking the appearance, texture, flavor, aftertaste, and overall acceptability of all tortillas. However, the appearance of control tortillas was preferred over commercial tortillas (P<0.01), whereas the aftertaste of commercial tortillas or those fortified with calcium carbonate was preferred over the control (P<0.05). Despite these differences, consumers were equally willing to purchase both fortified and nonfortified tortillas, suggesting that appearance and aftertaste may not influence willingness to purchase. Overall, this study shows that fortification of flour tortillas with various forms of calcium is a feasible alternative calcium source.

  19. Crystal growth and morphology of calcium oxalates and carbonates

    NARCIS (Netherlands)

    Heijnen, W.M.M.

    1986-01-01

    The main purpose of the research described in this thesis is to establish a relationship between the crystal structure and morphology of calcium oxalate and calcium carbonate crystals grown from aqueous solutions. Starting point is the PBC (Periodic Bond Chain) theory formulated by Hartman and Perdo

  20. Kinetics of the Carbonate Leaching for Calcium Metavanadate

    Directory of Open Access Journals (Sweden)

    Peiyang Shi

    2016-10-01

    Full Text Available The sodium salt roasting process was widely used for extracting vanadium due to its high yield rate of vanadium. However, the serious pollution was a problem. The calcium roasting process was environmentally friendly, but the yield rate of vanadium was relatively lower. Focusing on the calcium metavanadate produced in the calcium roasting process of vanadium minerals, the mechanism of the carbonate leaching for calcium metavanadate and its leaching kinetics of calcium metavanadate were studied. With the increase of the leaching agent content, the decrease of the particle size, the increase of the temperature and the increase of the reaction time, the leaching rate of vanadium increased, and the constant of reaction rate increased. In the carbonate leaching process, the calcium carbonate was globular and attached to the surface of calcium metavanadate. In the solution containing bicarbonate radical, lots of cracks formed in the dissolution process. However, the cracks were relatively fewer in the solution containing carbonate. In the present study, the carbonate leaching for calcium metavanadate was controlled by diffusion, the activation energy reached maximum and minimum in the sodium bicarbonate and the sodium carbonate solution, respectively. The activation energy value in the ammonium bicarbonate solution was between those two solutions. The kinetic equations of the carbonate leaching for calcium metavanadate were as follows: 1 − 2/3η − (1 − η2/3 = 4.39[Na2CO3]0.75/r0 × exp(−2527.06/Tt; 1 − 2/3η − (1 − η2/3 = 7.89[NaHCO3]0.53/r0 × exp(−2530.67/Tt; 1 − 2/3η − (1 − η2/3 = 6.78[NH4HCO3]0.69/r0 × exp(−2459.71/Tt.

  1. Calcium carbonate crystallisation at the microscopic level

    CERN Document Server

    Dobson, P S

    2001-01-01

    The primary concern of this thesis is the investigation of crystal nucleation and growth processes, and the effect of foreign substrates on the rate, extent and mechanism of crystallisation, with particular emphasis on the calcium carbonate system. A methodology, based on the in-line mixing of two stable solutions, which permits the continuous delivery of a solution with a constant, known supersaturation, has been developed and characterised. This has been used to induce CaCO sub 3 crystallisation in experimental systems involving the channel flow and wall jet techniques. The channel flow method has been adapted to facilitate the study of crystal growth at a single calcite crystal. Ca sup 2 sup + ion selective electrodes have been employed as a means of monitoring depletion of the supersaturated solution, downstream of the crystal substrate. The data obtained suggested a growth rate constant of 3x10 sup - sup 1 sup 2 mol cm sup - sup 2 s sup - sup 1 (and a reaction order of 1.52 on supersaturation). The ex-si...

  2. Nanoparticle tracers in calcium carbonate porous media

    KAUST Repository

    Li, Yan Vivian

    2014-07-15

    Tracers are perhaps the most direct way of diagnosing subsurface fluid flow pathways for ground water decontamination and for natural gas and oil production. Nanoparticle tracers could be particularly effective because they do not diffuse away from the fractures or channels where flow occurs and thus take much less time to travel between two points. In combination with a chemical tracer they can measure the degree of flow concentration. A prerequisite for tracer applications is that the particles are not retained in the porous media as the result of aggregation or sticking to mineral surfaces. By screening eight nanoparticles (3-100 nm in diameter) for retention when passed through calcium carbonate packed laboratory columns in artificial oil field brine solutions of variable ionic strength we show that the nanoparticles with the least retention are 3 nm in diameter, nearly uncharged, and decorated with highly hydrophilic polymeric ligands. The details of these column experiments and the tri-modal distribution of zeta potential of the calcite sand particles in the brine used in our tests suggests that parts of the calcite surface have positive zeta potential and the retention of negatively charged nanoparticles occurs at these sites. Only neutral nanoparticles are immune to at least some retention. © 2014 Springer Science+Business Media.

  3. Improving the compaction properties of roller compacted calcium carbonate.

    Science.gov (United States)

    Bacher, C; Olsen, P M; Bertelsen, P; Kristensen, J; Sonnergaard, J M

    2007-09-05

    The effects of roller compaction process parameters, morphological forms of calcium carbonate and particle size of sorbitol on flow, compaction and compression properties were investigated. The morphology of the calcium carbonate and the sorbitol particle size were more influential on the compaction properties than the settings of the roller compactor. The roller compaction process was demonstrated to be robust and stable in regard to flowability and compactibility. The flowability of the granules was improved adequately to facilitate compression in a production scale rotary tablet press. By adding sorbitol to the calcium carbonate, the compressibility - characterized by the Walker coefficient W(ID) - and the compactibility C(P) were improved considerably. A correlation between the consolidation characteristics was demonstrated. Compactibility data from the compaction simulator correlated with the tablet press for two of the calcium carbonates, the cubic form and the ground quality.

  4. Seeded Growth Route to Noble Calcium Carbonate Nanocrystal.

    Directory of Open Access Journals (Sweden)

    Aminul Islam

    Full Text Available A solution-phase route has been considered as the most promising route to synthesize noble nanostructures. A majority of their synthesis approaches of calcium carbonate (CaCO3 are based on either using fungi or the CO2 bubbling methods. Here, we approached the preparation of nano-precipitated calcium carbonate single crystal from salmacis sphaeroides in the presence of zwitterionic or cationic biosurfactants without external source of CO2. The calcium carbonate crystals were rhombohedron structure and regularly shaped with side dimension ranging from 33-41 nm. The high degree of morphological control of CaCO3 nanocrystals suggested that surfactants are capable of strongly interacting with the CaCO3 surface and control the nucleation and growth direction of calcium carbonate nanocrystals. Finally, the mechanism of formation of nanocrystals in light of proposed routes was also discussed.

  5. Calcium acetate versus calcium carbonate as phosphorus binders in patients on chronic haemodialysis: a controlled study.

    Science.gov (United States)

    Ring, T; Nielsen, C; Andersen, S P; Behrens, J K; Sodemann, B; Kornerup, H J

    1993-01-01

    The first reported double-blind cross-over comparison between the phosphorus binders calcium carbonate and calcium acetate was undertaken in 15 stable patients on chronic maintenance haemodialysis. Detailed registration of diet and analysis of the protein catabolic rate suggested an unchanged phosphorus intake during the study. It was found that predialytic serum phosphate concentration was significantly decreased by 0.11 mmol/l (0.34 mg/dl) (P = 0.021, 95% confidence limits 0.02-0.21 mmol/l; 0.06-0.65 mg/dl) during calcium acetate treatment. The calcium phosphate product was insignificantly decreased during treatment with calcium acetate whereas we could not exclude the possibility that calcium concentration had increased.

  6. Controlled Deposition and Alignment of Carbon Nanotubes

    Science.gov (United States)

    Smits, Jan M. (Inventor); Wincheski, Russell A. (Inventor); Patry, JoAnne L. (Inventor); Watkins, Anthony Neal (Inventor); Jordan, Jeffrey D. (Inventor)

    2012-01-01

    A carbon nanotube (CNT) attraction material is deposited on a substrate in the gap region between two electrodes on the substrate. An electric potential is applied to the two electrodes. The CNT attraction material is wetted with a solution defined by a carrier liquid having carbon nanotubes (CNTs) suspended therein. A portion of the CNTs align with the electric field and adhere to the CNT attraction material. The carrier liquid and any CNTs not adhered to the CNT attraction material are then removed.

  7. Cellular investigations on electrochemically deposited calcium phosphate composites.

    Science.gov (United States)

    Becker, Petra; Neumann, Hans-Georg; Nebe, Barbara; Lüthen, Frank; Rychly, Joachim

    2004-04-01

    Electrochemically deposited calcium phosphate (CaP) coatings are fast resorbable and existent only during the first period of osseointegration. In the present study, composite coatings with varying solubility (hydroxyapatite (HA), brushite with less HA and monetite (M) with less HA) were prepared and the influence of the degradation and the reprecipitation of CaP on osteoblastic cells were investigated. On the brushite composite coating a new precipitated, finely structured CaP phase was observed during immersion in cell culture medium with or without osteoblastic cells. The surface morphology of monetite and HA coatings were entirely unmodified under the same conditions. So it could be assumed that electrochemically deposited brushite with less HA acts as a precursor for new precipitated CaP. On this surface osteoblastic cells revealed a well-spread morphology with pronounced actin cytoskeleton and demonstrated good proliferation behaviour. Thus we suggest that brushite seems to be especially suitable for coating of implants as a matrix for nucleation and growth of new bone.

  8. The ANKH gene and familial calcium pyrophosphate dihydrate deposition disease.

    Science.gov (United States)

    Netter, Patrick; Bardin, Thomas; Bianchi, Arnaud; Richette, Pascal; Loeuille, Damien

    2004-09-01

    Familial calcium pyrophosphate dihydrate deposition (CPPD) disease is a chronic condition in which CPPD microcrystals deposit in the joint fluid, cartilage, and periarticular tissues. Two forms of familial CPPD disease have been identified: CCAL1 and CCAL2. The CCAL1 locus is located on the long arm of chromosome 8 and is associated with CPPD and severe osteoarthritis. The CCAL2 locus has been mapped to the short arm of chromosome 5 and identified in families from the Alsace region of France and the United Kingdom. The ANKH protein is involved in pyrophosphate metabolism and, more specifically, in pyrophosphate transport from the intracellular to the extracellular compartment. Numerous ANKH gene mutations cause familial CCAL2; they enhance ANKH protein activity, thereby elevating extracellular pyrophosphate levels and promoting the formation of pyrophosphate crystals, which produce the manifestations of the disease. Recent studies show that growth factors and cytokines can modify the expression of the normal ANKH protein. These results suggest a role for ANKH in sporadic CPPD disease and in CPPD associated with degenerative disease.

  9. The nacre protein perlucin nucleates growth of calcium carbonate crystals.

    Science.gov (United States)

    Blank, S; Arnoldi, M; Khoshnavaz, S; Treccani, L; Kuntz, M; Mann, K; Grathwohl, G; Fritz, M

    2003-12-01

    Atomic force microscopy (AFM) in aqueous solution was used to investigate native nacre of the marine snail Haliotis laevigata on the microscopic scale and the interaction of purified nacre proteins with calcium carbonate crystals on the nanoscopic scale. These investigations were controlled by scanning electron microscopy (SEM), light microscopy (LM) and biochemical methods. For investigations with AFM and SEM, nacre was cleaved parallel to the aragonite tablets in this biogenic polymer/mineral composite. Multilamellar organic sheets consisting of a core of chitin with layers of proteins attached on both sides lay between the aragonite layers consisting of confluent aragonite tablets. Cleavage appeared to occur between the aragonite tablet layer and the protein layer. AFM images revealed a honeycomb-like structure to the organic material with a diameter of the 'honeycombs' equalling that of the aragonite tablets. The walls of the structures consisted of filaments, which were suggested to be collagen. The flat regions of the honeycomb-like structures exhibited a hole with a diameter of more than 100 nm. When incubated in saturated calcium carbonate solution, aragonite needles with perfect vertical orientation grew on the proteinacous surface. After treatment with proteinase K, no growth of orientated aragonite needles was detected. Direct AFM measurements on dissolving and growing calcite crystals revealed a surface structure with straight steps the number of which decreased with crystal growth. When the purified nacre protein perlucin was added to the growth solution (a super-saturated calcium carbonate solution) new layers were nucleated and the number of steps increased. Anion exchange chromatography of the water-soluble proteins revealed a mixture of about 10 different proteins. When this mixture was dialysed against saturated calcium carbonate solution and sodium chloride, calcium carbonate crystals precipitated together with perlucin leaving the other proteins

  10. Atmospheric deposition of organic carbon via precipitation

    Science.gov (United States)

    Iavorivska, Lidiia; Boyer, Elizabeth W.; DeWalle, David R.

    2016-12-01

    Atmospheric deposition is the major pathway for removal of organic carbon (OC) from the atmosphere, affecting both atmospheric and landscape processes. Transfers of OC from the atmosphere to land occur as wet deposition (via precipitation) and as dry deposition (via surface settling of particles and gases). Despite current understanding of the significance of organic carbon inputs with precipitation to carbon budgets, transfers of organic matter between the atmosphere and land are not explicitly included in most carbon cycle models due to limited data, highlighting the need for further information. Studies regarding the abundance of OC in precipitation are relatively sparse, in part due to the fact that concentrations of organics in precipitation and their associated rates of atmospheric deposition are not routinely measured as a part of major deposition monitoring networks. Here, we provide a new data synthesis from 83 contemporary studies published in the peer reviewed literature where organic matter in precipitation was measured around the world. We compiled data regarding the concentrations of organic carbon in precipitation and associated rates of atmospheric deposition of organic carbon. We calculated summary statistics in a common set of units, providing insights into the magnitude and regional variability of OC in precipitation. A land to ocean gradient is evident in OC concentrations, with marine sites generally showing lower values than continental sites. Our synthesis highlights gaps in the data and challenges for data intercomparison. There is a need to concentrate sampling efforts in areas where anthropogenic OC emissions are on the rise (Asia, South America), as well as in remote sites suggesting background conditions, especially in Southern Hemisphere. It is also important to acquire more data for marine rainwater at various distances from the coast in order to assess a magnitude of carbon transfer between the land and the ocean. Our integration of

  11. Preparation and Characterization of a Calcium Carbonate Aerogel

    Directory of Open Access Journals (Sweden)

    Johann Plank

    2009-01-01

    Full Text Available We report on a facile method for the preparation of a calcium carbonate aerogel consisting of aggregated secondary vaterite particles with an approximate average diameter of 50 nm. It was synthesized via a sol-gel process by reacting calcium oxide with carbon dioxide in methanol and subsequent supercritical drying of the alcogel with carbon dioxide. The resulting monolith was opaque, brittle and had overall dimensions of 6×2×1 cm. It was characterized by X-ray powder diffraction, nitrogen adsorption method (BET, and scanning electron microscopy.

  12. Proliferation and differentiation of osteoblast-like MC3T3-E1 cells on biomimetically and electrolytically deposited calcium phosphate coatings.

    Science.gov (United States)

    Wang, Jiawei; de Boer, Jan; de Groot, Klaas

    2009-09-01

    Biomimetic and electrolytic deposition are versatile methods to prepare calcium phosphate coatings. In this article, we compared the effects of biomimetically deposited octacalcium phosphate and carbonate apatite coatings as well as electrolytically deposited carbonate apatite coating on the proliferation and differentiation of mouse osteoblast-like MC3T3-E1 cells. It was found that MC3T3-E1 cells cultured on the biomimetically deposited carbonate apatite coating demonstrated the greatest proliferation rate and the highest differentiation potential. Cells on the biomimetically deposited octacalcium phosphate coating had lower proliferation rate before day 7, but higher after that, than those on the electrolytically deposited carbonate apatite coating. There was no difference on the expression of early differentiation markers, that is, alkaline phosphatase activity and collagen content, between biomimetically deposited octacalcium phosphate and electrolytically deposited carbonate apatite coatings. However, higher expression of late differentiation markers, that is, osteocalcin and bone sialoprotein mRNA, was found on the biomimetically deposited octacalcium phosphate coating on day 14. These results suggest that the difference in in vitro osteoblast cell performance of calcium phosphate coatings might relate to their physicochemical properties. Biomimetic carbonate apatite coating is the most favorable surface for the proliferation and differentiation of MC3T3-E1 cells.

  13. Deposition of amorphous carbon-silver composites

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Zarco, O. [Instituto de Investigaciones en Materiales, Universidad Nacional Autonoma de Mexico, Circuito Exterior s/n, Ciudad Universitaria. 04510, Mexico D. F. Mexico (Mexico); Rodil, S.E., E-mail: ser42@iim.unam.m [Instituto de Investigaciones en Materiales, Universidad Nacional Autonoma de Mexico, Circuito Exterior s/n, Ciudad Universitaria. 04510, Mexico D. F. Mexico (Mexico); Camacho-Lopez, M.A. [Facultad de Quimica, Universidad Autonoma del Estado de Mexico, Tollocan s/n, esq. Paseo Colon, Toluca, Estado de Mexico, 50110 (Mexico)

    2009-12-31

    Composites of amorphous carbon films and silver were deposited by co-sputtering, where the target (10 cm diameter) was of pure graphite with small inclusion of pure silver (less than 1 cm{sup 2}). The films were deposited under different powers, from 40 to 250 W, and different target-substrate distances. The substrate was earthed and rotated in order to obtain a uniform distribution of the silver content. The addition of the Ag piece into the target increased the deposition rate of the carbon films, which could be related to the higher sputter yield of the silver, but there seems to be also a contribution from a larger emission of secondary electrons from the Ag that enhances the plasma and therefore the sputtering process becomes more efficient. Scanning electron micrographs acquired using backscattered electrons showed that the silver was segregated from the carbon matrix, forming nanoparticles or larger clusters as the power was increased. The X-ray diffraction pattern showed that the silver was crystalline and the carbon matrix remained amorphous, although for certain conditions a peak attributed to fullerene-like structures was obtained. Finally, we used Raman spectroscopy to understand the bonding characteristics of the carbon-silver composites, finding that there are variations in the D/G ratio, which can be correlated to the observed structure and X-ray diffraction results.

  14. Amorphous calcium carbonate controls avian eggshell mineralization: A new paradigm for understanding rapid eggshell calcification.

    Science.gov (United States)

    Rodríguez-Navarro, Alejandro B; Marie, Pauline; Nys, Yves; Hincke, Maxwell T; Gautron, Joel

    2015-06-01

    Avian eggshell mineralization is the fastest biogenic calcification process known in nature. How this is achieved while producing a highly crystalline material composed of large calcite columnar single crystals remains largely unknown. Here we report that eggshell mineral originates from the accumulation of flat disk-shaped amorphous calcium carbonate (ACC) particles on specific organic sites on the eggshell membrane, which are rich in proteins and sulfated proteoglycans. These structures known as mammillary cores promote the nucleation and stabilization of a amorphous calcium carbonate with calcitic short range order which predetermine the calcite composition of the mature eggshell. The amorphous nature of the precursor phase was confirmed by the diffuse scattering of X-rays and electrons. The nascent calcitic short-range order of this transient mineral phase was revealed by infrared spectroscopy and HRTEM. The ACC mineral deposited around the mammillary core sites progressively transforms directly into calcite crystals without the occurrence of any intermediate phase. Ionic speciation data suggest that the uterine fluid is equilibrated with amorphous calcium carbonate, throughout the duration of eggshell mineralization process, supporting that this mineral phase is constantly forming at the shell mineralization front. On the other hand, the transient amorphous calcium carbonate mineral deposits, as well as the calcite crystals into which they are converted, form by the ordered aggregation of nanoparticles that support the rapid mineralization of the eggshell. The results of this study alter our current understanding of avian eggshell calcification and provide new insights into the genesis and formation of calcium carbonate biominerals in vertebrates.

  15. Bioavailability of calcium supplements and the effect of Vitamin D: comparisons between milk, calcium carbonate, and calcium carbonate plus vitamin D.

    Science.gov (United States)

    Mortensen, L; Charles, P

    1996-03-01

    Our aim was to examine a regimen for calcium supplementation because various factors seem to be important for its bioavailability, and to examine the effect of adding vitamin D to the supplement. The participants were 20 healthy women aged 28-59 y (chi: 38 y). During the 3-d periods and 1 d before, the participants were consuming a calcium and energy-balanced diet as similar to their usual daily diet as possible. The study was designed as a randomized, placebo-controlled, partly blinded crossover study divided into four periods of 3 d each: 1) three tablets containing 1000 mg CaCO3/d, 2) three tablets containing 1000 mg CaCO3 plus 5 micrograms (200 IU) vitamin D/d, 3)1 L more milk than in the usual daily diet, and 4) three placebo tablets daily. Bioavailability of the different calcium-supplement regimens were evaluated by changes in 24-h urinary excretion of calcium, phosphate, and magnesium. A significant increase in urinary calcium excretion was found during all periods of supplementation compared with the placebo period (Pcalcium in the calcium carbonate period was not significantly higher that that in the milk period, but calcium carbonate plus vitamin D resulted in significantly higher calcium excretion compared with that in the milk period. We conclude that the examined calcium carbonate regimen is at least as good a calcium supplement as milk, and that addition of 600 IU vitamin D/d promptly resulted in an increase in urinary calcium excretion after an increase in calcium absorption, even in healthy women.

  16. Effect of substrate nature on the electrochemical deposition of calcium-deficient hydroxyapatites

    Science.gov (United States)

    Gualdrón-Reyes, A. F.; Domínguez-Vélez, V.; Morales-Morales, J. A.; Cabanzo, R.; Meléndez, A. M.

    2017-01-01

    Calcium phosphates were obtained by reducing nitrate ions to produce hydroxide ions on TiO2/stainless steel and TiO2/titanium electrodes. TiO2 coatings on metallic substrates were prepared by sol-gel dip-coating method. The morphology of deposits was observed by FESEM. Chemical nature of calcium phosphate deposits was identified by Raman micro-spectroscopy and FESEM/EDS microanalysis. Electrochemical behavior of nitrate and nitrite reduction on stainless steel and titanium electrodes was studied by linear sweep voltammetry. In addition, voltammetric study of the calcium phosphate electrodeposition on both electrodes was performed. From these measurements was selected the potential to form a calcium phosphate. A catalytic current associated to nitrate reduction reaction was obtained for stainless steel electrode, leading to significant deposition of calcium phosphate. Ca/P ratio for both substrates was less than 1.67. The formation of calcium deficient hydroxyapatite was confirmed by Raman spectroscopy.

  17. Release of Crude Oil from Silica and Calcium Carbonate Surfaces

    DEFF Research Database (Denmark)

    Liu, Xiaoyan; Yan, Wei; Stenby, Erling Halfdan;

    2016-01-01

    Adsorption and desorption of a North Sea crude oil to silica and calcium carbonate surfaces were studied by a quartz crystal microbalance, while the bare surfaces and adsorbed oil layers were characterized by atomic force microscopy and contact angle measurements. Water contact angles were measured...... on the bare surfaces, surfaces with an adsorbed oil layer, and surfaces after being exposed to aqueous salt solutions. This showed that the silica surface became more hydrophobic after oil adsorption, while the wettability of the calcium carbonate surface was not significantly changed by adsorption of an oil...... layer. A surface energy component analysis based on the acid base theory showed that oil adsorption on the surfaces depends upon apolar, acidic, and basic oil components of the crude oil and that the adsorbed oil components differ for adsorption to silica and calcium carbonate. Desorption of the crude...

  18. Hard Carbon Films Deposited under Various Atmospheres

    Science.gov (United States)

    Wei, M.-K.; Chen, S.-C.; Wu, T. C.; Lee, Sanboh

    1998-03-01

    Using a carbon target ablated with an XeCl-excimer laser under various gas atmospheres at different pressures, hard carbon was deposited on silicon, iron and tungsten carbide substrates. The hardness, friction coefficient, and wear rate of the film against steel are better than pure substrate material, respectively, so that it has potential to be used as a protective coating for micromechanical elements. The influences of gas pressure, gas atmosphere, and power density of laser irradiation on the thermal stability of film were analyzed by means of Raman-spectroscope, time-of-flight method, and optical emission spectrum. It was found that the film deposited under higher pressure has less diamond-like character. The film deposited under rest gas or argon atmosphere was very unstable and looked like a little graphite-like character. The film deposited at high vacuum (10-5 mbar rest gas) was the most stable and looked like the most diamond-like character. The film deposited at higher power density was more diamond-like than that at lower power density.

  19. THE CLINICAL MANIFESTATIONS OF CALCIUM PYROPHOSPHATE CRYSTAL DEPOSITION DISEASE

    Directory of Open Access Journals (Sweden)

    F. M. Kudaeva

    2014-01-01

    Full Text Available Objective: to provide the clinical characteristics of joint injury in patients with calcium pyrophosphate crystal (CPC deposition disease.Subjects and methods. The trial enrolled 68 patients (43 women, 25 men with a verified diagnosis of CPC deposition disease. Their mean age was 60.2±11.8 years and disease duration was 7.5±6.4 years. Examination revealed the presence of arthritis and arthralgias. Polarizing microscopy with an Olympus CX31-P compensator was used to detectcrystals in synovial fluid. X-ray study of the knee joints was performed in the anteroposterior and lateral projections and that of the hand joints was in the frontal projection, Ultrasonography (USG of the knee and wrist joints was done using a GE Voluson-I transducer.Results. A concurrence of arthritis and arthralgias was noted in 37 (54% patients; 24 (36% patients had arthralgias only; 7 (10% had arthritis only. Arthritis affecting the knee, wrist, ankle, and first metacarpophalangeal joints was observed in 53, 15, 12, and 6% of cases, respectively. There was acute arthritis in 18% of the patients and chronic arthritis in 39%; the rate of CPC osteoarthrosis was 43%. Joint USG diagnosed knee and wrist joint chondrocalcinosis in 94 and 56% of the patients, respectively. USG could reveal asymptomatic wrist joint chondrocalcinosis significantly more often (in 56 and 17% of the patients, respectively; p = 0.008. Besides, USG could visualize synovitis in the knee joints in 88% of the patients with isolated arthralgias in them and synovitis in the wrinkle joints in 52% of the patients without clinical signs of inflammation in them.Conclusion. Osteoarthrosis is the most common form of CPC deposition disease. Knee joints in this disease are most frequently involved. Joint USG is of more informative value in detecting chondrocalcinosis than X-ray study; USG can also identify synovitis in the intact joints.

  20. Effect of carbon fiber on calcium phosphate bone cement

    Institute of Scientific and Technical Information of China (English)

    戴红莲; 王欣宇; 黄健; 闫玉华; 李世普

    2004-01-01

    The calcium phosphate cement (α-TCP/TTCP) was reinforced with oxidation-treated carbon fibers. The effect of aspect ratio and content of carbon fiber on the compression strength and bending strength of the hardened body was discussed. The results show that the reinforcing effect is optimal as the aspect ratio is 375 and the additive amount is 0.3% (mass fraction). Under this condition, the compressive strength is increased by 55% (maximum 63.46 MPa), and the bending strength is nearly increased by 100% (maximum 11.95 MPa), respectively. However, if the additive quantity and aspect ratio are too high, the effect of the carbon fibers is limited because it can not be dispersed uniformly in the hardened body. The biological evaluation indicates that the calcium phosphate cement reinforced by carbon fibers has good biocompatibility.

  1. Correlation between calcium carbonate content and emission characteristics of incense.

    Science.gov (United States)

    Yang, Chi-Ru; Lin, Ta-Chang; Chang, Feng-Hsiang

    2006-12-01

    In Taiwan and China, calcium carbonate is commonly added as a filler during incense production to lower the cost. This study has found an unexpected benefit for this practice: it reduces particulate emission. Nine types of the popular incense on the local market were chosen for this study. The calcium content in raw material incense was analyzed by inductively coupled plasma atomic emission spectrometry, followed by X-ray diffraction (XRD) spectroscopy. The correlation between the calcium content and emission characteristics of incense was investigated. The calcium content varied from 1.8 to 60 mg/g (incense burned) among those nine different types of incense. Very little calcium (incense. Instead, most calcium was artificially added in the form of CaCO3 during manufacturing. The combustion characteristics, including burning rate, emission factors of particulate, ash, and solid-phase polycyclic aromatic hydrocarbons (S-PAHs), varied significantly among the nine types of incense. Incense containing 2% calcium would emit 30% less S-PAHs, compared with those with little (incense by approximately 50%.

  2. CALCIUM CARBONATE DISSOLUTION RATE IN LIMESTONE CONTACTORS

    Science.gov (United States)

    The rate of carbonate mineral dissolution from limestone was studied using a rotating disk apparatus and samples of limestone of varied composition. The purpose of this study was to determine the effect of limestone composition on the kinetics of carbonate mineral dissolution. Th...

  3. Rocky Mountain Carbonate Spring Deposit development

    Science.gov (United States)

    Rainey, Dustin Kyle

    Relict Holocene carbonate spring deposits containing diverse biotic and abiotic depositional textures are present at Fall Creek cold sulphur springs, Alberta, Fairmont Hot Springs, British Columbia, and Hot Creek cold springs, British Columbia. The relict deposits are formed mainly of low-magnesium crystalline calcite contained in laterally continuous strata. Paleo-flow regimes were characterized by extensive sheet flow that increased the surface area of spring water exposed to the atmosphere. Calcite precipitated inorganically from spring water that attained CaCO3 supersaturation through agitation-induced CO2 degassing that was facilitated by elevated flow rates and a large surface area as spring water flowed down-slope. Thus, the deposits contain only minor amounts of detrital, mechanically deposited, and biogenic carbonate. Evaporation was only a minor contributor to CaCO3 supersaturation, mainly in quiescent environments. Photosynthetic CO2 removal did not measurably contribute to CaCO3 supersaturation. Calcite crystals precipitated in biotic facies formed from low to moderately supersaturated spring water, whereas abiotic dendrite crystals formed rapidly from highly supersaturated spring water. Calcite passively nucleated on cyanobacteria, bryophytes and macrophytes, and was probably facilitated by cyanobacterial extracellular polymeric substances. Cyanobacterial filaments and stromatolites are integral parts of all three deposits, whereas bryophytes were restricted to the Fall Creek and Hot Creek deposits. Diagenetic microbial degradation of crystalline calcite was common to all three deposits, but recrystallization was limited to the Fall Creek deposit. The amount and location of calcite precipitation relative to the vents was controlled by the concentrations of Ca2+ and HCO3- in solution, and discharge volume fluctuations. Spring water with high [Ca2+] and [HCO 3-] precipitated large amounts of calcite proximal to the vents (e.g. Fairmont), whereas spring

  4. The effect of magnetic field on electrochemically deposited calcium phosphate/collagen coatings.

    Science.gov (United States)

    Zhao, Xueni; He, Jianpeng; Zhang, Jing; Wang, Xudong; Wang, Wanying

    2014-01-01

    Nanostructured calcium phosphate/collagen (CaP/COL) coatings were deposited on the carbon/carbon (C/C) composites through electrochemical deposition (ECD) under magnetic field. The effect of magnetic fields with different orientations on the morphology and composition was investigated. Both the morphology and composition of the coatings could be altered by superimposed magnetic field. Under zero magnetic field and magnetic field, three-dimensional network structure consisting of collagen fibers and CaP were formed on the C/C substrate. The applied magnetic field in the electric field helped to form nanostructured and plate-like CaP on collagen fibers. For the ECD under magnetic field, the Ca/P molar ratio of the coatings was lower than the one under B=0. This may be contributed to the decreased electrical resistance or the increased electrical conductivity of electrolyte solutions under magnetic field. The nanosized CaP/COL coatings exhibited the similar morphology to the human bone and could present excellent cell bioactivity and osteoblast functions.

  5. Formate oxidation driven calcium carbonate precipitation by Methylocystis parvus OBBP

    NARCIS (Netherlands)

    Ganendra, G; De Muynck, W; Ho, A.; Arvaniti, EC; Hosseinkhani, B; Ramos, JA; Rahier, H; Boon, N.

    2014-01-01

    Microbially Induced Carbonate Precipitation (MICP) applied in the construction industry poses several disadvantages such as ammonia release to the air and nitric acid production. An alternative MICP from calcium formate by Methylocystis parvus OBBP is presented in this study to overcome these disadv

  6. Protein mapping of calcium carbonate biominerals by immunogold

    NARCIS (Netherlands)

    Marin, Frédéric; Pokroy, Boaz; Luquet, Gilles; Layrolle, Pierre; Groot, de Klaas

    2007-01-01

    The construction of metazoan calcium carbonate skeletons is finely regulated by a proteinaceous extracellular matrix, which remains embedded within the exoskeleton. In spite of numerous biochemical studies, the precise localization of skeletal proteins has remained for a long time as an elusive goal

  7. Calcium carbonate microspheres as carriers for the anticancer drug camptothecin

    Energy Technology Data Exchange (ETDEWEB)

    Qiu, Neng [Division of Biomedical Engineering, School of Engineering, University of Glasgow, Glasgow, G12 8LT (United Kingdom); State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, West China Medical School, Sichuan University, Chengdu 610041 (China); Department of Bio-pharmaceutical Engineering, School of Chemical Engineering, Sichuan University, Chengdu ,610065 (China); Yin, Huabing, E-mail: huabing.yin@glasgow.ac.uk [Division of Biomedical Engineering, School of Engineering, University of Glasgow, Glasgow, G12 8LT (United Kingdom); Ji, Bozhi; Klauke, Norbert; Glidle, Andrew [Division of Biomedical Engineering, School of Engineering, University of Glasgow, Glasgow, G12 8LT (United Kingdom); Zhang, Yongkui; Song, Hang [Department of Bio-pharmaceutical Engineering, School of Chemical Engineering, Sichuan University, Chengdu ,610065 (China); Cai, Lulu; Ma, Liang; Wang, Guangcheng [State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, West China Medical School, Sichuan University, Chengdu 610041 (China); Chen, Lijuan, E-mail: lijuan17@hotmail.com [State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, West China Medical School, Sichuan University, Chengdu 610041 (China); Wang, Wenwen [State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, West China Medical School, Sichuan University, Chengdu 610041 (China)

    2012-12-01

    Biogenic calcium carbonate has come to the attention of many researchers as a promising drug delivery system due to its safety, pH sensitivity and the large volume of information already in existence on its medical use. In this study, we employed bovine serum albumin (BSA) as an additive to synthesize a series of porous calcium carbonate microspheres (CCMS). These spheres, identified as vaterite, are stable both in aqueous solutions and organic solvents. Camptothecin, an effective anticancer agent, was loaded into the CCMS by simple diffusion and adsorption. The camptothecin loaded CCMS showed sustained cell growth inhibitory activity and a pH dependent release of camptothecin. With a few hours, the release is negligible under physiological conditions (pH = 7.4) but almost complete at pH 4 to 6 (i.e. pHs found in lysosomes and solid tumor tissue respectively). These findings suggest that porous, biogenic calcium carbonate microspheres could be promising carriers for the safe and efficient delivery of anticancer drugs of low aqueous solubility. - Highlights: Black-Right-Pointing-Pointer BSA-doped calcium carbonate microspheres with porous structure were prepared. Black-Right-Pointing-Pointer Camptothecin was encapsulated in the spherical microparticles with encapsulation efficiency up to 11%. Black-Right-Pointing-Pointer The release of encapsulated camptothecin is pH dependent Black-Right-Pointing-Pointer In vitro studies showed an effective anticancer activity of the camptothecin- microspheres.

  8. Para-amino benzoic acid–mediated synthesis of vaterite phase of calcium carbonate

    Indian Academy of Sciences (India)

    T N Ramesh; S A Inchara; K Pallavi

    2015-05-01

    Calcium carbonate polymorphs were precipitated at room temperature and 80°C by varying the precipitation pH, carbonate source, effect of solvent in presence and absence of structure directing agent such as para-aminobenzoic acid. Calcite phase of calcium carbonate was obtained when sodium hydrogen carbonate and/or sodium carbonate (used as precipitating agents) were added to calcium chloride solution at different pHs in water and/or methanol as solvent in separate experiments. Vaterite phase of calcium carbonate (CaCO3) has been synthesized by mixing calcium chloride and sodium carbonate in presence of para-aminobenzoic acid when water–methanol binary mixture was used as solvent. Vaterite phase of calcium carbonate crystallizes in P63/mmc, while that of calcite phase in R-3mc, respectively. Calcite phase of calcium carbonate exhibits rhombohedral morphology, while vaterite phase has spherical morphology.

  9. 40 CFR 415.300 - Applicability; description of the calcium carbonate production subcategory.

    Science.gov (United States)

    2010-07-01

    ... resulting from the production of calcium carbonate by the milk of lime process and by the recovery process... calcium carbonate production subcategory. 415.300 Section 415.300 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Calcium Carbonate Production Subcategory § 415.300 Applicability; description of...

  10. Influence of surface treatment of carbon fibers on electrochemical crystallization of calcium phosphate

    Institute of Scientific and Technical Information of China (English)

    TAO Ke; HUANG Su-ping; ZHOU Ke-chao

    2005-01-01

    Electrodeposition technique was used to coat calcium phosphate on carbon fiber which can be used to reinforce hydroxyapatite. The differences between fibers treated with and without nitric acid in electrodeposition were evaluated. The X-ray diffractometry results show that CaHPO4·2H2O is obtained as the kind of calcium phosphate coating on carbon fiber. The scanning electron microscopy photographs and deposit kinetic curve indicate that the influences of the functional group attained by nitric acid treatment, the crystal morphology and crystallization of the coating layers on the fiber with and without treatment rate are obviously different. The functional group, especially the acidic group, can act as nucleation centers of electrochemical crystallization.

  11. Heat mass transfer model of fouling process of calcium carbonate on heat transfer surface

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    A new heat mass transfer model was developed to predict the fouling process of calcium carbonate on heat transfer surface. The model took into account not only the crystallization fouling but also the particle fouling which was formed on the heat transfer surface by the suspension particles of calcium carbonate in the su- persaturated solution. Based on experimental results of the fouling process, the deposition and removal rates of the mixing fouling were expressed. Furthermore, the coupling effect of temperature with the fouling process was considered in the physics model. As a result the fouling resistance varying with time was obtained to describe the fouling process and the prediction was compared with experimental data under same conditions. The results showed that the present model could give a good prediction of fouling process, and the deviation was less than 15% of the experimental data in most cases. The new model is credible to predict the fouling process.

  12. Calcium carbonate as a possible dosimeter for high irradiation doses

    Energy Technology Data Exchange (ETDEWEB)

    Negron M, A.; Ramos B, S.; Camargo R, C. [UNAM, Instituto de Ciencias Nucleares, Ciudad Universitaria, 04510 Mexico D. F. (Mexico); Uribe, R. M. [Kent State University, College of Technology, Kent OH (United States); Gomez V, V. [UNAM, Instituto de Quimica, Ciudad Universitaria, 04510 Mexico D. F. (Mexico); Kobayashi, K., E-mail: negron@nucleares.unam.mx [Yokohama National University (Japan)

    2014-08-15

    The aim of this work is to analyze the interactions of 5 MeV electron beam radiation and a 290 MeV/u Carbon beam with calcium carbonate (powder) at 298 K and at different irradiation doses, for the potential use of calcium carbonate as a high-dose dosimeter. The irradiation doses with the electron beam were from 0.015 to 9 MGy, and with Carbon beam from 1.5 kGy to 8 kGy. High-energy radiation induces the formation of free radicals in solid calcium carbonate that can be detected and measured by electron paramagnetic resonance (EPR). An increase of the EPR response for some of the free radicals produced in the sample was observed as a function of the irradiation dose. The response of one of the radicals decreased with the dose. These measurements are reproducible; the preparation of the sample is simple and inexpensive; and the signal is stable for several months. The response curves show that the dosimeter tends to saturate at 10 MGy. Based on these properties, we propose this chemical compound as a high-dose dosimeter, mainly for electron irradiation. (author)

  13. Fate of Organic Carbon Deposited in Reservoirs

    Science.gov (United States)

    Huntington, T. G.; Rhoton, F. E.; Bennett, S. J.; Hudnall, W. H.

    2002-05-01

    Sedimentation of soil organic carbon (SOC) eroded from uplands and deposited in reservoirs could be an important mechanism for carbon sequestration provided that it is conserved during transport and burial and that uplands are not experiencing net loss. There are uncertainties in both these assumptions and gaining a better understanding of these processes is a key objective of ongoing carbon-cycle investigations. The U.S. Geological Survey, the U. S. Department of Agriculture, and Louisiana State University Agricultural Center are collaborating on an investigation of soils and sediments in the Yalobusha River Basin in Mississippi. Sediment cores were collected from upland soils and from Grenada Lake, a flood control reservoir, in the basin. Suspended sediments have been collected from the Yalobusha River and one of its tributaries upstream of the lake. We are measuring carbon mineralization potential in conjunction with carbon and nitrogen concentrations, 13C, mineralogy, and texture on sediments and upland soils to determine whether eroding SOC is conserved or oxidized during transport and burial. Differences in mineralization potential and other chemical and physical properties are used to infer net changes in the original eroding SOC. Autochthonous production of SOC within reservoirs could replace labile SOC oxidized during transport and burial thereby masking losses due to oxidation. Autochthonous sources can be evaluated by chemical and physical characterization of the sediments. Stable carbon isotope (13C) geochemistry provides a tool for distinguishing the two primary sources of organic carbon incorporated in lake sediments because allochthonous SOC from the surrounding watershed is, in general, less depleted in stable 13C than autochthonous SOC produced in the lake by aquatic organisms such as macrophytes and phytoplankton. The integration of the 13C signature recorded in the organic fraction of the lake sediments with total organic carbon, C/N ratio

  14. Microanalyses of the hydroxyl—poly—calcium sodium phosphate coatings produced by ion beam assisted deposition

    Institute of Scientific and Technical Information of China (English)

    LIUZhong-Yang; WANGChang-Xing; 等

    2002-01-01

    Thin calcium phosphate catings on titanium alloy substrates were prepared by Ar+ ion beam assisted deposition(IBAD) from hydroxyl-poly-calcium sodium phosphate(HPPA) target.The coatings were analyzed by XRD,FTIR,XPS,These analyses revealed that the as-deposited films were amorphous or no apparent crystallinity.No distinct absorption band of the hydroxyl group was observed in FTIR spectra of the coatings but new absorption bands were presented for CO3-2,The calcium to phosphorous ratio of these catings in different IBAD conditions varied from 0.46 to 3.36.

  15. Intraosseous secondary calcium salt crystal deposition: an artefact of acid decalcification.

    Science.gov (United States)

    Keen, C E; Crocker, P R; Brady, K; Buk, S J; Levison, D A

    1995-08-01

    We previously observed, in decalcificated bone specimens, intraosseous crystal deposits with morphological and analytical similarity to calcium pyrophosphate dihydrate. We have now been able, by a combination of more detailed morphological studies of these and similar cases, and by infrared spectroscopy in three cases, to show that this is, in fact deposition of the secondary calcium salts brushite and monetite, occurring as an artefact during formic acid decalcification. Our earlier postulate of bone as an additional primary crystallization site for calcium pyrophosphate dihydrate is effectively disproved. This artefact deserves wider recognition.

  16. Preparation of Bioactive Calcium Phosphate Coating on Porous C/C Substrate by a Novel Deposition Technique

    Institute of Scientific and Technical Information of China (English)

    XIONG Xinbo; ZENG Xierong; LI Xiaohua; Xie Shenghui; ZOU Chunli

    2008-01-01

    A novel heat substrate technique,high frequency inductive heat deposition(IHD),was introduced to coat porous carbon materials,C/C and carbon felt to improve their bioactivity.The morphologies,composition and microstructure of the resulting coatings were examined by scanning electron microscopy(SEM),energy dispersive spectra(EDS),X-ray diffractometer(XRD)and Fourier transform infrared spectroscopy (FTIR).The results show that,the calcium phosphate consisted of non-stoichiometric,CO3-containing and plate-like octacalcium phosphate(Ca8-xH2(PO4)6,OCP)could uniformly cover the entire porous surfaces of carbon materials.Good adhesion of the coating to carbon material substrates was observed.

  17. DEPOSITION CARBON NANOSTRUCTURES BY SURFATRON GENERATED DISCHARGE

    Directory of Open Access Journals (Sweden)

    Marina Davydova

    2014-12-01

    Full Text Available Carbon nanostructures were deposited by surface wave discharge using various Ar/CH4/ CO2 gas mixture ratios. The morphology was controlled by adjusting of gas concentration and was investigated by scanning electron microscopy (SEM. Also, the influence of the low temperature plasma treatment and process time on the wettability of the diamond films has been studied. The results indicate that for hydrogen termination of diamond surface indicate that the temperature as low as 400°C and treatment time of 15 min is sufficient to attain the p-type surface conductivity of diamond.

  18. Preliminary Nanosims Analysis of Carbon Isotope of Carbonates in Calcium-Aluminum-Rich Inclusions

    OpenAIRE

    Guan, Y.; Paque, J. M.; Burnett, D.S.; Eiler, J. M.

    2009-01-01

    Carbonate minerals observed in primitive meteorites are products of either terrestrial weathering or aqueous alteration in the early solar system. Most of the carbonate minerals in carbonaceous chondrites occur primarily as isolated grains in matrix, as crosscutting veins, or as replacement minerals in chondrules [e.g., 1, 2]. A few calcium-aluminum-rich inclusions (CAIs) have been reported containing carbonate minerals as well [2, 3]. The C and O isotopes of carbonates in c...

  19. Rapid, high-temperature, field test method for evaluation of geothermal calcium carbonate scale inhibitors

    Energy Technology Data Exchange (ETDEWEB)

    Asperger, R.G.

    1986-09-01

    A new test method is described that allows the rapid field testing of calcium carbonate scale inhibitors at 500/sup 0/F (260/sup 0/C). The method evolved from use of a full-flow test loop on a well with a mass flow rate of about 1 x 10/sup 6/ lbm/hr (126 kg/s). It is a simple, effective way to evaluate the effectiveness of inhibitors under field conditions. Five commercial formulations were chosen for field evaluation on the basis of nonflowing, laboratory screening tests at 500/sup 0/F (260/sup 0/C). Four of these formulations from different suppliers controlled calcium carbonate scale deposition as measured by the test method. Two of these could dislodge recently deposited scale that had not age-hardened. Performance-profile diagrams, which were measured for these four effective inhibitors, show the concentration interrelationship between brine calcium and inhibitor concentrations at which the formulations will and will not stop scale formation in the test apparatus. With these diagrams, one formulation was chosen for testing on the full-flow brine line. The composition was tested for 6 weeks and showed a dramatic decrease in the scaling occurring at the flow-control valve. This scaling was about to force a shutdown of a major, long-term flow test being done for reservoir economic evaluations. The inhibitor stopped the scaling, and the test was performed without interruption.

  20. Deposition of the platinum crystals on the carbon nanotubes

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    A new technique and the affecting factors for depositing platinum on the carbon nanotubes were investigated. The results show that the deposited platinum crystals in the atmosphere of hydrogen or nitrogen have a small size and a homogeneous distribution on the surface of the carbon nanotubes. The pretreatment would decrease the platinum particles on the carbon nanotubes significantly.

  1. Mechano-activated surface modification of calcium carbonate in wet stirred mill and its properties

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Surface modification of calcium carbonate particles using sodium stearate(SDS) as a modification agent incorporated with the simultaneous wet ultra-fine grinding in the laboratory stirred mill was investigated. The physical properties and application properties of modified calcium carbonate were measured and evaluated. The action mechanism between SDS and calcium carbonate in the modification was studied by infrared spectrometry(IR) and X-ray photoelectron energy spectroscopy(XPS). The results indicate that the crushing mechanic force intensity can obviously influence the modification effect of calcium carbonate because of mechano-chemical effect. The hydrophilic surface of calcium carbonate is turned into hydrophobic after modification. The properties of polyethylene(PE) filled by modified calcium carbonate powder is markedly improved. And the adsorption of SDS could occur by chemical reaction with calcium carbonate surface.

  2. Carbon Dioxide Adsorption by Calcium Zirconate at Higher Temperature

    Directory of Open Access Journals (Sweden)

    K. B. Kale

    2012-12-01

    Full Text Available The CO2 adsorption by calcium zirconate was explored at pre- and post- combustion temperature condition. The several samples of the calcium zirconate were prepared by different methods such as sol-gel, solid-solid fusion, template and micro-emulsion. The samples of the calcium zirconate were characterized by measurement of surface area, alkalinity/acidity, and recording the XRD patterns and SEM images. The CO2 adsorptions by samples of the calcium zirconate were studied in the temperature range 100 to 850 oC and the CO2 adsorptions were observed in the ranges of 6.88 to 40.6 wt % at 600 0C and 8 to 16.82 wt% at in between the temperatures 200 to 300 oC. The effect of Ca/Zr mol ratio in the samples of the calcium zirconate on the CO2 adsorption and alkalinity were discussed. The adsorbed moisture by the samples of the calcium zirconate was found to be useful for the CO2 adsorption. The promoted the samples of the calcium zirconate by K+, Na+, Rb+, Cs+, Ag+ and La3+ showed the increased CO2 adsorption. The exposure time of CO2 on the samples of the calcium zirconate showed the increased CO2 adsorption. The samples of the calcium zirconate were found to be regenerable and reusable several times for the adsorption of CO2 for at the post- and pre-combustion temperature condition. Copyright © 2012 by BCREC Undip. All rights reservedReceived: 23rd June 2012, Revised: 28th August 2012, Accepted: 30th August 2012[How to Cite: K. B. Kale, R. Y. Raskar, V. H. Rane and A. G.  Gaikwad (2012. Carbon Dioxide Adsorption by Calcium Zirconate at Higher Temperature. Bulletin of Chemical Reaction Engineering & Catalysis, 7 (2: 124-136. doi:10.9767/bcrec.7.2.3686.124-136] [How to Link / DOI: http://dx.doi.org/10.9767/bcrec.7.2.3686.124-136 ] | View in 

  3. Multiwalled Carbon Nanotube Deposition on Model Environmental Surfaces

    Science.gov (United States)

    Deposition of multiwalled carbon nanotubes (MWNTs) on model environmental surfaces was investigated using a quartz crystal microbalance with dissipation monitoring (QCM-D). Deposition behaviors of MWNTs on positively and negatively charged surfaces were in good agreement with Der...

  4. Biomaterial-Derived Calcium Carbonate Nanoparticles for Enteric Drug Delivery

    OpenAIRE

    Diane Render; Temesgen Samuel; Howard King; Madan Vig; Shaik Jeelani; Ramapuram Jayachandra Babu; Vijaya Rangari

    2016-01-01

    Oral drug delivery systems provide the most convenient, noninvasive, readily acceptable alternatives to parenteral systems. In the current work, eggshell-derived calcium carbonate (CaCO3) nanoparticles were used to develop enteric drug delivery system in the form of tablets. CaCO3 nanoparticles were manufactured using top-down ball-milling method and characterized by X-ray diffractometry (XRD) and transmission electron microscopy (TEM) and loaded with 5-fluorouracil as a model drug. Tablets w...

  5. Compactibility of agglomerated mixtures of calcium carbonate and microcrystalline cellulose.

    Science.gov (United States)

    Garzón Serra, María de Lourdes; Villafuerte Robles, Leopoldo

    2003-06-04

    The tablet tensile strength (T) of agglomerated mixtures of microcrystalline cellulose-Avicel PH 102 (MC), calcium carbonate (CC) and polyvinylpyrrolidone (Povidone, PVP), lubricated with magnesium stearate (MS), and formed under a compaction pressure (P(c)) ranging up to 618MPa has been determined. The compactibility was defined through: ln(-ln(1-T/T(max)))=Slope x lnP(c)+Intercept. MC/CC mixtures added of an agglutinant, before and after lubrication, show an important positive effect on their tablet tensile strength compared to a lineal relationship. This positive effect becomes smaller with decreasing compaction pressures. By different mixing methods, the higher the mixing efficiency the higher the compactibility, following the order: spray-dried>wet massing>tumble mixing. The compactibility of MC/CC/PVP spray-dried mixtures with calcium carbonate content from 20 to 60% was equal to or greater than that of pure microcrystalline cellulose. After lubrication with 2% MS the compactibility decreased, only the mixture with the maximal tablet tensile strength attained the tensile strength of pure microcrystalline cellulose. The presence of the binder, the lubricant and higher compaction pressures allow the accommodation of higher calcium carbonate proportions in the mixtures, at the maximal tablet tensile strength of the series. The lubricant decreases in a greater extent the compactibility of mixtures with a continuous phase of MC/PVP than that of CC/PVP. This is attributed to the plastic behavior of the MC/PVP continuous phase compared to a calcium carbonate continuous phase able to disrupt the Povidone and the possible lubricant coatings allowing a stronger interparticle interaction.

  6. Effect of some organic solvent-water mixtures composition on precipitated calcium carbonate in carbonation process

    Science.gov (United States)

    Konopacka-Łyskawa, Donata; Kościelska, Barbara; Karczewski, Jakub

    2015-05-01

    Precipitated calcium carbonate particles were obtained during carbonation of calcium hydroxide slurry with carbon dioxide. Aqueous solutions of isopropyl alcohol, n-butanol and glycerol were used as solvents. Concentration of organic additives in the reactive mixture was from 0% to 20% (vol). Precipitation process were performed in a stirred tank reactor equipped with gas distributor. Multimodal courses of particles size distribution were determined for produced CaCO3 particles. Calcium carbonate as calcite was precipitated in all experiments. The mean Sauter diameter of CaCO3 particles decreased when the concentration of all used organic additives increased. The amount of small particle fraction in the product increased with the increasing concentration of organic solvents. Similar physical properties of used liquid phase resulted in the similar characteristics of obtained particles.

  7. Mechanical properties of polypropylene/calcium carbonate nanocomposites

    Directory of Open Access Journals (Sweden)

    Daniel Eiras

    2009-01-01

    Full Text Available The aim of this work was to study the influence of calcium carbonate nanoparticles in both tensile and impact mechanical properties of a polypropylene homopolymer. Four compositions of PP/CaCO3 nanocomposites were prepared in a co-rotational twin screw extruder machine with calcium carbonate content of 3, 5, 7 and 10 wt. (% The tests included SEM analyzes together with EDS analyzer and FTIR spectroscopy for calcium carbonate, tensile and impact tests for PP and the nanocomposites. The results showed an increase in PP elastic modulus and a little increase in yield stress. Brittle-to-ductile transition temperature was reduced and the impact resistance increased with the addition of nanoparticles. From the stress-strain curves we determined the occurrence of debonding process before yielding leading to stress softening. Debonding stress was determined from stress-strain curves corresponding to stress in 1% strain. We concluded that the tensile properties depend on the surface contact area of nanoparticles and on their dispersion. Finally we believe that the toughening was due to the formation of diffuse shear because of debonding process.

  8. Preparation of calcium carbonate particles coated with titanium dioxide

    Institute of Scientific and Technical Information of China (English)

    Hai Lin; Ying-bo Dong; Le-yong Jiang

    2009-01-01

    The preparation of a new mineral composite material, calcium carbonate particles coated with titanium dioxide, was stud-ied. The mechanism of the preparation process was proposed. The new mineral composite material was made by the mechanochemi-eal method under the optimum condition that the mass ratio of calcium carbonate particles to titanium dioxide was 6.5:3.5. The mass ratios of two different types of titanium dioxide (anatase to rutile) and grinding media to grinded materials were 8:2 and 4:1 respec-tively, and the modified density was 60%. Under this condition, the new material was capable of forming after 120-min modification.The hiding power and oil absorption of this new material were 29.12 g/m~2 and 23.30%, respectively. The results show that the modi-fication is based on surface hydroxylation. After coating with titanium dioxide, the hiding power of calcium carbonate can be im-proved greatly. The new mineral composite materials can be used as the substitute for titanium dioxide.

  9. lectrolytic deposition of lithium into calcium phosphate coatings

    NARCIS (Netherlands)

    Wang, Jiawei; Groot, de Klaas; Blitterswijk, van Clemens; Boer, de Jan

    2009-01-01

    Objectives: Lithium ions stimulate the Wnt signaling pathway and the authors previously demonstrated that lithium enhances the proliferation of tissue cultured human mesenchymal stem cells. The aim of this study was to prepare and characterize a calcium phosphate/lithium coating by means of electrol

  10. Coaxial carbon plasma gun deposition of amorphous carbon films

    Science.gov (United States)

    Sater, D. M.; Gulino, D. A.; Rutledge, S. K.

    1984-01-01

    A unique plasma gun employing coaxial carbon electrodes was used in an attempt to deposit thin films of amorphous diamond-like carbon. A number of different structural, compositional, and electrical characterization techniques were used to characterize these films. These included scanning electron microscopy, scanning transmission electron microscopy, X ray diffraction and absorption, spectrographic analysis, energy dispersive spectroscopy, and selected area electron diffraction. Optical absorption and electrical resistivity measurements were also performed. The films were determined to be primarily amorphous, with poor adhesion to fused silica substrates. Many inclusions of particulates were found to be present as well. Analysis of these particulates revealed the presence of trace impurities, such as Fe and Cu, which were also found in the graphite electrode material. The electrodes were the source of these impurities. No evidence of diamond-like crystallite structure was found in any of the film samples. Details of the apparatus, experimental procedure, and film characteristics are presented.

  11. Development of poly(aspartic acid-co-malic acid) composites for calcium carbonate and sulphate scale inhibition.

    Science.gov (United States)

    Mithil Kumar, N; Gupta, Sanjay Kumar; Jagadeesh, Dani; Kanny, K; Bux, F

    2015-01-01

    Polyaspartic acid (PSI) is suitable for the inhibition of inorganic scale deposition. To enhance its scale inhibition efficiency, PSI was modified by reacting aspartic acid with malic acid (MA) using thermal polycondensation polymerization. This reaction resulted in poly(aspartic acid-co-malic acid) (PSI-co-MA) dual polymer. The structural, chemical and thermal properties of the dual polymers were analysed by using scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, differential scanning calorimetry and gel permeation chromatography. The effectiveness of six different molar ratios of PSI-co-MA dual polymer for calcium carbonate and calcium sulphate scale inhibition at laboratory scale batch experiments was evaluated with synthetic brine solution at selected doses of polymer at 65-70°C by the static scale test method. The performance of PSI-co-MA dual polymer for the inhibition of calcium carbonate and calcium sulphate precipitation was compared with that of a PSI single polymer. The PSI-co-MA exhibited excellent ability to control inorganic minerals, with approximately 85.36% calcium carbonate inhibition and 100% calcium sulphate inhibition at a level of 10 mg/L PSI-co-MA, respectively. Therefore, it may be reasonably concluded that PSI-co-MA is a highly effective scale inhibitor for cooling water treatment applications.

  12. Randomized crossover study comparing the phosphate-binding efficacy of calcium ketoglutarate versus calcium carbonate in patients on chronic hemodialysis.

    Science.gov (United States)

    Bro, S; Rasmussen, R A; Handberg, J; Olgaard, K; Feldt-Rasmussen, B

    1998-02-01

    The objective of the study was to evaluate the phosphate-binding efficacy, side effects, and cost of therapy of calcium ketoglutarate granulate as compared with calcium carbonate tablets in patients on chronic hemodialysis. The study design used was a randomized, crossover open trial, and the main outcome measurements were plasma ionized calcium levels, plasma phosphate levels, plasma intact parathyroid hormone (PTH) levels, requirements for supplemental aluminum-aminoacetate therapy, patient tolerance, and cost of therapy. Nineteen patients on chronic hemodialysis were treated with a dialysate calcium concentration of 1.25 mmol/L and a fixed alfacalcidol dose for at least 2 months. All had previously tolerated therapy with calcium carbonate. Of the 19 patients included, 10 completed both treatment arms. After 12 weeks of therapy, the mean (+/-SEM) plasma ionized calcium level was significantly lower in the ketoglutarate arm compared with the calcium carbonate arm (4.8+/-0.1 mg/dL v 5.2+/-0.1 mg/dL; P = 0.004), whereas the mean plasma phosphate (4.5+/-0.3 mg/dL v 5.1+/-0.1 mg/dL) and PTH levels (266+/-125 pg/mL v 301+/-148 pg/mL) did not differ significantly between the two treatment arms. Supplemental aluminum-aminoacetate was not required during calcium ketoglutarate treatment, while two patients needed this supplement when treated with calcium carbonate. Five of 17 (29%) patients were withdrawn from calcium ketoglutarate therapy within 1 to 2 weeks due to intolerance (anorexia, vomiting, diarrhea, general uneasiness), whereas the remaining 12 patients did not experience any side effects at all. The five patients with calcium ketoglutarate intolerance all had pre-existing gastrointestinal symptoms; four of them had received treatment with cimetidine or omeprazol before inclusion into the study. Calculations based on median doses after 12 weeks showed that the cost of the therapy in Denmark was 10 times higher for calcium ketoglutarate compared with calcium

  13. Influence of deposited CNTs on the surface of carbon fiber by ultrasonically assisted electrophoretic deposition

    Science.gov (United States)

    Jiang, J. J.; Liu, F.; Deng, C.; Fang, L. C.; Li, D. J.

    2015-07-01

    The surface property of carbon fiber directly affects the interface performance between carbon fiber and matrix. To improve the surface property of carbon fiber, we proposed a simple method to prepare carbon nanotubes /carbon fiber hybrid fiber via ultrasonically assisted electrophoretic deposition (EPD). Surface morphologies and surface functional group of carbon fibers were examined by atomic force microscopy (AFM), scanning electron microscopy (SEM) and fourier transform infrared spectrometer (FTIR), respectively. The results show that the deposition of carbon nanotubes changed the surface morphologies of carbon fibers and introduced polar groups (C=O and C-O) to carbon fiber surface. Comparing the results with EPD-only, ultrasonically assisted EPD increased the uniformity of carbon nanotubes coatings whereas only sparse and not uniformly deposition formed without ultrasonic.

  14. Effect of Cationic and Anionic Surfactants on the Application of Calcium Carbonate Nanoparticles in Paper Coating

    CERN Document Server

    Barhoum, Ahmed; Abou-Zaied, Ragab Esmail; Rehan, Mohamed; Dufour, Thierry; Hill, Gavin; Dufresne, Alain

    2016-01-01

    Modification of calcium carbonate particles with surfactant significantly improves the properties of the calcium carbonate coating on paper. Unmodified and CTAB and oleate-modified calcium carbonate nanoparticles were prepared using the wet carbonation technique for paper coating. CTAB (cationic surfactant) and sodium oleate (anionic surfactant) were used to modify the size, morphology, and surface properties of the precipitated nanoparticles. The obtained particles were characterized by XRD, FT-IR spectroscopy, zeta potential measurements, TGA and TEM. Coating colors were formulated from the prepared unmodified and modified calcium carbonates and examined by creating a thin coating layer on reference paper. The effect of calcium carbonate particle size and surface modification on paper properties, such as coating thickness, coating weight, surface roughness, air permeability, brightness, whiteness, opacity, and hydrophobicity, were investigated and compared with GCC calcium carbonate-coated papers. The obtai...

  15. Renal histopathology and crystal deposits in patients with small bowel resection and calcium oxalate stone disease.

    Science.gov (United States)

    Evan, Andrew P; Lingeman, James E; Worcester, Elaine M; Bledsoe, Sharon B; Sommer, Andre J; Williams, James C; Krambeck, Amy E; Philips, Carrie L; Coe, Fredric L

    2010-08-01

    We present here the anatomy and histopathology of kidneys from 11 patients with renal stones following small bowel resection, including 10 with Crohn's disease and 1 resection in infancy for unknown cause. They presented predominantly with calcium oxalate stones. Risks of formation included hyperoxaluria (urine oxalate excretion greater than 45 mg per day) in half of the cases, and acidic urine of reduced volume. As was found with ileostomy and obesity bypass, inner medullary collecting ducts (IMCDs) contained crystal deposits associated with cell injury, interstitial inflammation, and papillary deformity. Cortical changes included modest glomerular sclerosis, tubular atrophy, and interstitial fibrosis. Randall's plaque (interstitial papillary apatite) was abundant, with calcium oxalate stone overgrowth similar to that seen in ileostomy, idiopathic calcium oxalate stone formers, and primary hyperparathyroidism. Abundant plaque was compatible with the low urine volume and pH. The IMCD deposits all contained apatite, with calcium oxalate present in three cases, similar to findings in patients with obesity bypass but not an ileostomy. The mechanisms for calcium oxalate stone formation in IMCDs include elevated urine and presumably tubule fluid calcium oxalate supersaturation, but a low calcium to oxalate ratio. However, the mechanisms for the presence of IMCD apatite remain unknown.

  16. Ultrastructural evidence for transepithelial calcium transport in the anterior sternal epithelium of the terrestrial isopod Porcellio scaber (Crustacea) during the formation and resorption of CaCO3 deposits

    Science.gov (United States)

    Ziegler

    1996-05-20

    Before the molt, terrestrial isopods store large amounts of calcium carbonate between the epithelium and the old cuticle of the first four anterior sternites. In order to test whether the anterior sternal epithelium has specific structural differentiations indicative of transepithelial ion transport, the anterior sternal epithelium and, as a control, the posterior sternal epithelium were studied using electron-microscopical techniques. During the formation of calcium carbonate deposits, the basolateral plasma membrane of the anterior sternal epithelium forms an elaborate interconnected network of interstitial dilations and channels. Numerous osmiophilic granules occur within this basolateral intercellular network during resorption of the calcium carbonate deposits. Electron energy-loss spectroscopy of the osmiophilic granules indicates that they contain calcium. During the resorption of the calcium carbonate deposits, the apical plasma membrane of the anterior sternal epithelium has many subcuticular folds. An interstitial network, osmiophilic granules, and apical, subcuticular folds do not occur in the posterior sternal epithelium. Taken together, these structural features are indicative of transepithelial ion transport and are probably necessary for the formation and resorption of the anterior sternal calcium carbonate deposits.

  17. Effect of calcium on adsorption capacity of powdered activated carbon.

    Science.gov (United States)

    Li, Gang; Shang, Junteng; Wang, Ying; Li, Yansheng; Gao, Hong

    2013-12-01

    We investigated the effect of calcium ion on the adsorption of humic acid (HA) (as a target pollutant) by powered activated carbon. The HA adsorption isotherms at different pH and kinetics of two different solutions including HA alone and HA doped Ca(2+), were performed. It was showed that the adsorption capacity of powdered activated carbon (PAC) for HA was markedly enhanced when Ca(2+) was doped into HA. Also, HA and Ca(2+) taken as nitrate were tested on the uptake of each other respectively and it was showed that the adsorbed amounts of both of them were significantly promoted when HA and calcium co-existed. Furthermore, the adsorbed amount of HA slightly decreased with the increasing of Ca(2+) concentration, whereas the amount of calcium increased with the increasing of HA concentration, but all above the amounts without addition. Finally, the change of pH before and after adsorption process is studied. In the two different solutions including HA alone and HA doped Ca(2+), pH had a small rise, but the extent of pH of later solution was bigger.

  18. New agent to treat elevated phosphate levels: magnesium carbonate/calcium carbonate tablets.

    Science.gov (United States)

    Meyer, Caitlin; Cameron, Karen; Battistella, Marisa

    2012-01-01

    In summary, Binaphos CM, a magnesium carbonate/calcium carbonate combination phosphate binder, is marketed for treating elevated phosphate levels in dialysis patients. Although studies using magnesium/calcium carbonate as a phosphate binder are short term with small numbers of patients, this phosphate binder has shown some promising results and may provide clinicians with an alternative for phosphate binding. Using a combination phosphate binder may reduce pill burden and encourage patient compliance. In addition to calcium and phosphate, it is imperative to diligently monitor magnesium levels in patients started on this medication, as magnesium levels may increase with longer duration of use. Additional randomized controlled trials are necessary to evaluate long-term efficacy and safety of this combination phosphate binder.

  19. Randomized crossover study comparing the phosphate-binding efficacy of calcium ketoglutarate versus calcium carbonate in patients on chronic hemodialysis

    DEFF Research Database (Denmark)

    Bro, S; Rasmussen, R A; Handberg, J

    1998-01-01

    The objective of the study was to evaluate the phosphate-binding efficacy, side effects, and cost of therapy of calcium ketoglutarate granulate as compared with calcium carbonate tablets in patients on chronic hemodialysis. The study design used was a randomized, crossover open trial, and the main...

  20. Effect of calcium carbonate on hardening, physicochemical properties, and in vitro degradation of injectable calcium phosphate cements.

    NARCIS (Netherlands)

    Sariibrahimoglu, K.; Leeuwenburgh, S.C.G.; Wolke, J.G.C.; Yubao, L.; Jansen, J.A.

    2012-01-01

    The main disadvantage of apatitic calcium phosphate cements (CPCs) is their slow degradation rate, which limits complete bone regeneration. Carbonate (CO(3)(2)(-)) is the common constituent of bone and it can be used to improve the degradability of the apatitic calcium phosphate ceramics. This study

  1. Conversion of calcium sulphide to calcium carbonate during the process of recovery of elemental sulphur from gypsum waste.

    Science.gov (United States)

    de Beer, M; Maree, J P; Liebenberg, L; Doucet, F J

    2014-11-01

    The production of elemental sulphur and calcium carbonate (CaCO3) from gypsum waste can be achieved by thermally reducing the waste into calcium sulphide (CaS), which is then subjected to a direct aqueous carbonation step for the generation of hydrogen sulphide (H2S) and CaCO3. H2S can subsequently be converted to elemental sulphur via the commercially available chemical catalytic Claus process. This study investigated the carbonation of CaS by examining both the solution chemistry of the process and the properties of the formed carbonated product. CaS was successfully converted into CaCO3; however, the reaction yielded low-grade carbonate products (i.e. 99 mass% as CaCO3) or precipitated calcium carbonate (PCC).

  2. A comparative study of calcium absorption following a single serving administration of calcium carbonate powder versus calcium citrate tablets in healthy premenopausal women

    Directory of Open Access Journals (Sweden)

    Haiyuan Wang

    2014-04-01

    Full Text Available Background: Calcium is an essential mineral often taken as a daily, long-term nutritional supplement. Data suggests that once-daily dosing is important with regard to long-term compliance of both drugs and nutritional supplements. Objective: This study was undertaken to compare the bioavailability of a single serving of two calcium supplements in healthy, premenopausal women. Design: A two-period, crossover bioavailability study of a single serving of calcium citrate tablets (two tablets=500 mg calcium versus a single serving of calcium carbonate powder (one packet of powder=1,000 mg calcium was performed in healthy women aged between 25 and 45. All subjects were on a calcium-restricted diet 7 days prior to testing and fasted for 12 h before being evaluated at 0, 1, 2, and 4 h after oral administration of the test agents. Blood measurements for total and ionized calcium and parathyroid hormone were performed and adverse events were monitored. Results: Twenty-three women were evaluable with a mean age of 33.2±8.71. Results showed that administration of a single serving of a calcium carbonate powder resulted in greater absorption in total and ionized calcium versus a single serving of calcium citrate tablets at 4 h (4.25±0.21 vs. 4.16±0.16, p=0.001. There were minimal side effects and no reported serious adverse events. Conclusions: This study shows that a single serving of a calcium carbonate powder is more bioavailable than a single serving of calcium citrate tablets. This may be beneficial for long-term compliance.

  3. Calcium carbonate-calcium phosphate mixed cement compositions for bone reconstruction.

    Science.gov (United States)

    Combes, C; Bareille, R; Rey, C

    2006-11-01

    The feasibility of making calcium carbonate-calcium phosphate (CaCO(3)-CaP) mixed cements, comprising at least 40% (w/w) CaCO(3) in the dry powder ingredients, has been demonstrated. Several original cement compositions were obtained by mixing metastable crystalline CaCO(3) phases with metastable amorphous or crystalline CaP powders in aqueous medium. The cements set within at most 1 h at 37 degrees C in atmosphere saturated with water. The hardened cement is microporous and exhibits weak compressive strength. The setting reaction appeared to be essentially related to the formation of a highly carbonated nanocrystalline apatite phase by reaction of the metastable CaP phase with part or almost all of the metastable CaCO(3) phase. The recrystallization of metastable CaP varieties led to a final cement consisting of a highly carbonated poorly crystalline apatite analogous to bone mineral associated with various amounts of vaterite and/or aragonite. The presence of controlled amounts of CaCO(3) with a higher solubility than that of the apatite formed in the well-developed CaP cements might be of interest to increase resorption rates in biomedical cement and favors its replacement by bone tissue. Cytotoxicity testing revealed excellent cytocompatibility of CaCO(3)-CaP mixed cement compositions.

  4. Crystal structures of calcium hemicarboaluminate and carbonated calcium hemicarboaluminate from synchrotron powder diffraction data.

    Science.gov (United States)

    Runčevski, Tomče; Dinnebier, Robert E; Magdysyuk, Oxana V; Pöllmann, Herbert

    2012-10-01

    One of the main phases formed at the beginning of the carbonation reaction of cementitious building materials is the calcium hemicarboaluminate (abbreviated as Hc). This AFm (shorthand for hydrated calcium aluminate phases structurally related to hydrocalumite) phase was synthesized, crystallized and then studied by synchrotron X-ray powder diffraction and micro-Raman spectroscopy. At room temperature and standard experimental conditions two major cementitious phases were detected, the Hc phase (as a major phase) and carbonated calcium hemicarboaluminate (abbreviated as cHc). By increasing the temperature the Hc form transforms into cHc. The crystal structures of these important AFm phases were successfully solved and refined in the R3c space group of the trigonal crystal system. Hc has the unit-cell parameters a = 5.7757 (1) and c = 48.812 (2) Å, and cHc the unit-cell parameters a = 5.7534 (1) and c = 46.389 (1) Å. The two crystal structures are composed of positively charged main layers, [Ca(4)Al(2)(OH)(12)](2+), and negatively charged interlayers, [OH(2n)(CO(3))(1 - n)·4H(2)O](2-). The structure of the main layers is typical of the AFm family. Conversely, the interlayer region has a characteristic structure built up from water molecules and statistically distributed anions. In the interlayer, the Hc carbonate and hydroxyl anions are distributed in a 0.25:0.5 ratio, whereas the ratio of the anions in the cHc interlayers is 0.4:0.2.

  5. Crystalline calcium carbonate and hydrogels as microenvironment for stem cells.

    Science.gov (United States)

    Astachov, Liliana; Nevo, Zvi; Aviv, Moran; Vago, Razi

    2011-01-01

    Stem cell development and fate decisions are dictated by the microenvironment in which the stem cell is embedded. Among the advanced goals of tissue engineering is the creation of a microenvironment that will support the maintenance and differentiation of the stem cell--based on embryonic and adult stem cells as potent, cellular sources--for a variety of clinical applications. This review discusses some of the approaches used to create regulatory and instructive microenvironments for the directed differentiation of mesenchymal stem cells (MSCs) using three-dimensional crystalline calcium carbonate biomaterials of marine origin combined with a hydrated gel based on hyaluronan.

  6. Effects of temperature during the irradiation of calcium carbonate

    Energy Technology Data Exchange (ETDEWEB)

    Negron M, A.; Camargo R, C.; Ramos B, S. [UNAM, Instituto de Ciencias Nucleares, Circuito Exterior, Ciudad Universitaria, 04510 Mexico D. F. (Mexico); Gomez V, V. [UNAM, Instituto de Quimica, Ciudad Universitaria, 04510 Mexico D. F. (Mexico); Uribe, R. M., E-mail: negron@nucleares.unam.mx [Kent State University, College of Technology, Kent 44240 Ohio (United States)

    2015-10-15

    The gamma irradiation of calcium carbonate at different doses (0 to 309 kGy) and temperature regimes (77 K to 298 K) was carried out to study the effects of irradiation temperature. The changes were followed by EPR spectroscopy. We observed the formation of a composite EPR spectrum even at low radiation doses and temperature. There is a strong effect on the evaluation of the radicals formed as a function of irradiation temperature, probably due to the diffusion in the frozen powder. Response curves show that this system tends to saturate at 10 MGy at 298 K. (Author)

  7. Preparation and properties of gluten/calcium carbonate composites

    Institute of Scientific and Technical Information of China (English)

    Min Zuo; Zheng Zheng Lai; Yi Hu Song; Qiang Zheng

    2008-01-01

    Environment friendly thermosetting composites were prepared by blending wheat gluten (WG) as matrix, calcium carbonate (CaCO3) as filler and glycerol as plasticizer followed by compression molding the mixture at 120 ℃ to crosslink the WG matrix. Morphology observation showed that the CaCO3 particles were finely dispersed in matrix. Incorporation of CaCO3 up to 10 wt% into the composites caused Young's modulus and tensile strength to increase markedly. On the other hand, the moisture absorption and elongation at break decreased slightly.

  8. [Use of domestically produced corn starch in the manufacture of calcium carbonate tablets].

    Science.gov (United States)

    Gazikalović, E; Obrenović, D; Nidzović, Z; Toskić-Radojicić, M

    1998-01-01

    The results of the testing of calcium carbonate tablets, compounded with starch as the binding and decay substance are presented. The content of calcium carbonate in the tablets, as well as the mass varying, solidity, prodigality and aptness to decay were determined. The best properties were observed in the tablets with 15% starch mucilage, added suddenly, in the whole amount, to the prepared mixture of calcium carbonate and lactose. This procedure is fast and simple, and compound tablets of calcium carbonate are of regulated quality.

  9. Regulation of Microstructure of Calcium Carbonate Crystals by Egg White Protein

    Institute of Scientific and Technical Information of China (English)

    ZHU Wen-kun; LUO Xue-gang; ZHANG Chi; DUAN Tao; ZHOU Jian

    2012-01-01

    Crystal growth of calcium carbonate in biological simulation was investigated via egg white protein with different volume fractions,during which calcium carbonate was synthesized by calcium chloride and sodium carbonate.The morphology,thermal properties and microstructure of the calcium carbonate micro-to-nanoscale crystals were characterized by scanning electron microscopy(SEM),transmission electron microscopy(TEM),Fourier transform infrared spectroscopy(FTIR),thermogravimetric analysis(TG)and X-ray diffraction(XRD)analysis.The results show that the volume fraction of egg white protein has great influence on the shape,size and morphology of calcium carbonate crystals.The calcium carbonate crystals were the mixtures of calcite-vaterite-like crystals including spherical and rough surface,which are different from that formed in pure water.With the increase of egg white protein concentration,the diameter of calcium carbonate crystals changed,the amount of formed spherical calcium carbonate particles decreased and that of vaterite increased.These results indicate that the coordination and electrostatic interaction between egg white protein and Ca2+ significantly affect the calcium carbonate crystalization.

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

    CERN Document Server

    Day, Sarah J; 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 calcium carbonate phase vaterite was formed alongside calcite, at elevated CO2 pressure, at room temperature and subsequently remained stable over a large range of temperature and pressure. We report the formation of the calcium carbonate mineral vaterite whilst attempting to simulate carbonate dust grain formation in astrophysical environments. This suggests that vaterite could be a mineral component of carbonate dust and also presents a possible method of formation for vaterite and its polymorphs on planetary surfaces.

  11. Calcium pyrophosphate dihydrate deposition disease (CPPD/Pseudogout of the temporomandibular joint - FNA findings and microanalysis.

    Directory of Open Access Journals (Sweden)

    Naqvi Asghar

    2008-01-01

    Full Text Available We report a case of a Calcium pyrophosphate dihydrate deposition disease (CPPD presenting as a mass in the parotid and temporomandibular joint (TMJ that simulated a parotid tumor. A 35 year-old man presented with pain in the left ear area. A CT Scan of the area showed a large, calcified mass surrounding the left condylar head, and extending into the infratemporal fossa. FNA of the mass showed birefringent crystals, most of which were rhomboid with occasional ones being needle shaped, embedded in an amorphous pink substance. Scanning electron microscopy (SEM with energy dispersive x-ray spectroscopy (EDS of these crystals showed peaks corresponding to calcium and phosphorus. SEM/EDS is a rapid method of diagnosing calcium pyrophosphate dihydrate deposition disease (CPPD and an alternative to more commonly used method of special staining of cell block sections coupled with polarizing microscopy.

  12. Calcium Carbonate Production by Coccolithophorid Alge in Long Term Carbon Dioxide Sequestration

    Energy Technology Data Exchange (ETDEWEB)

    V. J. Fabry

    2006-09-30

    Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

  13. Calcium Carbonate Produced by Coccolithophorid Algae in Long Term, Carbon Dioxide Sequestration

    Energy Technology Data Exchange (ETDEWEB)

    V.J. Fabry

    2007-06-30

    Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO2 through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids - single-celled, marine algae that are the major global producers of calcium carbonate - to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

  14. CALCIUM CARBONATE PRODUCTION BY COCCOLITHOPHORID ALGAE IN LONG TERM, CARBON DIOXIDE SEQUESTRATION

    Energy Technology Data Exchange (ETDEWEB)

    V.J. Fabry

    2004-10-30

    Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds or bioreactors to abate CO{sub 2} emissions from power plants.

  15. CALCIUM CARBONATE PRODUCTION BY COCCOLITHOPHORID ALGAE IN LONG TERM CARBON DIOXIDE SEQUESTRATION

    Energy Technology Data Exchange (ETDEWEB)

    V. J. Fabry

    2003-10-30

    Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds or bioreactors to abate CO{sub 2} emissions from power plants.

  16. CALCIUM CARBONATE PRODUCTION BY COCCOLITHAPHORID ALGAE IN LONG TERM, CARBON DIOXIDE SEQUESTRATION

    Energy Technology Data Exchange (ETDEWEB)

    V. J.Fabry

    2004-01-30

    Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

  17. CALCIUM CARBONATE PRODUCTION BY COCCOLITHOPHORID ALGAE IN LONG TERM, CARBON DIOXIDE SEQUESTRATION

    Energy Technology Data Exchange (ETDEWEB)

    V.J. Fabry

    2004-04-26

    Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids single-celled, marine algae that are the major global producers of calcium carbonate to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

  18. Carbonate-containing apatite (CAP) synthesis under moderate conditions starting from calcium carbonate and orthophosphoric acid

    Energy Technology Data Exchange (ETDEWEB)

    Pham Minh, Doan, E-mail: doan.phamminh@mines-albi.fr [Université de Toulouse, Mines Albi, CNRS, Centre RAPSODEE, Campus Jarlard, F-81013 Albi cedex 09 (France); Tran, Ngoc Dung; Nzihou, Ange [Université de Toulouse, Mines Albi, CNRS, Centre RAPSODEE, Campus Jarlard, F-81013 Albi cedex 09 (France); Sharrock, Patrick [Université de Toulouse, SIMAD, IUT Paul Sabatier, Avenue Georges Pompidou, 81104 Castres (France)

    2013-07-01

    The synthesis of carbonate-containing apatite (CAP) from calcium carbonate and orthophosphoric acid under moderate conditions was investigated. In all cases, complete precipitation of orthophosphate species was observed. The reaction temperature influenced strongly the decomposition of calcium carbonate and therefore the composition of formed products. The reaction temperature of 80 °C was found to be effective for the complete decomposition of calcium carbonate particles after 48 h of reaction. Infra-red spectroscopy (IR), nuclear magnetic resonance (NMR), thermogravimetry/mass spectroscopy (TG–MS) coupling, and X-ray diffraction (XRD) characterizations allowed the identification of the composition of formed products. By increasing the reaction temperature from 20 °C to 80 °C, the content of A-type CAP increased and that of B-type CAP decreased, according to the favorable effect of temperature on the formation of A-type CAP. The total amount of carbonate content incorporated in CAP's structure, which was determined by TG–MS analysis, increased with the reaction temperature and reached up to 4.1% at 80 °C. At this temperature, the solid product was mainly composed of apatitic components and showed the typical flat-needle-like structure of CAP particles obtained in hydrothermal conditions. These results show an interesting one-step synthesis of CAP from calcium carbonate and orthophosphoric acid as low cost but high purity starting materials. Highlights: • The synthesis of carbonate-containing apatites from CaCO{sub 3} and H{sub 3}PO{sub 4} was studied. • The decomposition of CaCO{sub 3} particles was complete at 80 °C, 13.2 bar for 48 h. • The transformation of CaCO{sub 3} and H{sub 3}PO{sub 4} into apatitic products was also complete. • Pure carbonate-containing apatite was directly obtained without water-rising step.

  19. Study of calcium carbonate and sulfate co-precipitation

    KAUST Repository

    Zarga, Y.

    2013-06-01

    Co-precipitation of mineral based salts in scaling is still not well understood and/or thermodynamically well defined in the water industry. This study focuses on investigating calcium carbonate (CaCO3) and sulfate mixed precipitation in scaling which is commonly observed in industrial water treatment processes including seawater desalination either by thermal-based or membrane-based processes. Co-precipitation kinetics were studied carefully by monitoring several parameters simultaneously measured, including: pH, calcium and alkalinity concentrations as well as quartz microbalance responses. The CaCO3 germination in mixed precipitation was found to be different than that of simple precipitation. Indeed, the co-precipitation of CaCO3 germination time was not anymore related to supersaturation as in a simple homogenous precipitation, but was significantly reduced when the gypsum crystals appeared first. On the other hand, the calcium sulfate crystals appear to reduce the energetic barrier of CaCO3 nucleation and lead to its precipitation by activating heterogeneous germination. However, the presence of CaCO3 crystals does not seem to have any significant effect on gypsum precipitation. IR spectroscopy and the Scanning Electronic Microscopy (SEM) were used to identify the nature of scales structures. Gypsum was found to be the dominant precipitate while calcite and especially vaterite were found at lower proportions. These analyses showed also that gypsum crystals promote calcite crystallization to the detriment of other forms. © 2013 Elsevier Ltd.

  20. Analysis of barium hydroxide and calcium hydroxide slurry carbonation reactors

    Energy Technology Data Exchange (ETDEWEB)

    Patch, K.D.; Hart, R.P.; Schumacher, W.A.

    1980-05-01

    The removal of CO/sub 2/ from air was investigated by using a continuous-agitated-slurry carbonation reactor containing either barium hydroxide (Ba(OH)/sub 2/) or calcium hydroxide (Ca(OH)/sub 2/). Such a process would be applied to scrub /sup 14/CO/sub 2/ from stack gases at nuclear-fuel reprocessing plants. Decontamination factors were characterized for reactor conditions which could alter hydrodynamic behavior. An attempt was made to characterize reactor performance with models assuming both plug flow and various degrees of backmixing in the gas phase. The Ba(OH)/sub 2/ slurry enabled increased conversion, but apparently the process was controlled under some conditions by phenomena differing from those observed for carbonation by Ca(OH)/sub 2/. Overall reaction mechanisms are postulated.

  1. Evaluating the Contributions of Atmospheric Deposition of Carbon and Other Nutrients to Nitrification in Alpine Environments

    Science.gov (United States)

    Oldani, K. M.; Mladenov, N.; Williams, M. W.

    2013-12-01

    The Colorado Front Range of the Rocky Mountains contains undeveloped, barren soils, yet in this environment there is strong evidence for a microbial role in increased nitrogen (N) export. Barren soils in alpine environments are severely carbon-limited, which is the main energy source for microbial activity and sustenance of life. It has been shown that atmospheric deposition can contain high amounts of organic carbon (C). Atmospheric pollutants, dust events, and biological aerosols, such as bacteria, may be important contributors to the atmospheric organic C load. In this stage of the research we evaluated seasonal trends in the chemical composition and optical spectroscopic (fluorescence and UV-vis absorbance) signatures of snow, wet deposition, and dry deposition in an alpine environment at Niwot Ridge in the Rocky Mountains of Colorado to obtain a better understanding of the sources and chemical character of atmospheric deposition. Our results reveal a positive trend between dissolved organic carbon concentrations and calcium, nitrate and sulfate concentrations in wet and dry deposition, which may be derived from such sources as dust and urban air pollution. We also observed the presence of seasonally-variable fluorescent components that may be attributed to fluorescent pigments in bacteria. These results are relevant because atmospheric inputs of carbon and other nutrients may influence nitrification in barren, alpine soils and, ultimately, the export of nitrate to alpine watersheds.

  2. Pulsed laser deposition of carbon nanotube and polystyrene-carbon nanotube composite thin films

    Science.gov (United States)

    Stramel, A. A.; Gupta, M. C.; Lee, H. R.; Yu, J.; Edwards, W. C.

    2010-12-01

    In this work, we report on the fabrication of carbon nanotube thin films via pulsed laser deposition using a pulsed, diode pumped, Tm:Ho:LuLF laser with 2 μm wavelength. The thin films were deposited on silicon substrates using pure carbon nanotube targets and polystyrene-carbon nanotube composite targets. Raman spectra, scanning electron micrographs, and transmission electron micrographs show that carbon nanotubes are present in the deposited thin films, and that the pulsed laser deposition process causes minimal degradation to the quality of the nanotubes when using pure carbon nanotube targets.

  3. Scaling and Removal of Calcium Carbonate on Electroless Plating Surface

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The scaling process of calcium carbonate on a low-energy heat transfer surface-electroless plating surface was investigated in a simulated cooling water system. Owing to the very low surface energy, the electroless plating surface exhibited less scaling susceptibility. A longer induction period and a lower scaling rate were obtained on the low-energy surface compared to copper surface under identical conditions. The calcite particles obtained on the electroless plating surface during the induction period were larger in size than those on copper surface because fewer crystals formed and grew at the same time on the low-energy surface. With increasing surface temperature, the induction period reduced and the scaling rate increased for the low-energy surface. When initial surface temperature was fixed, an increase in fluid velocity would reduce the induction period and increase the scaling rate due to the diffusion effect. However, when the heat flux was fixed, an increase in fluid velocity would decrease the surface temperature, and lead to a longer induction period and a lower scaling rate. The removal experiments of calcium carbonate scale indicated that during post induction period, the detachment was not obvious, while during the induction period, apparent removal of crystal particles was obtained on the electroless plating surface owing to the weak adhesion force. The more frequently the transient high hydrodynamic force acted, the more the detached crystal particles were.

  4. DECOMPOSITION STUDY OF CALCIUM CARBONATE IN COCKLE SHELL

    Directory of Open Access Journals (Sweden)

    MUSTAKIMAH MOHAMED

    2012-02-01

    Full Text Available Calcium oxide (CaO is recognized as an efficient carbon dioxide (CO2 adsorbent and separation of CO2 from gas stream using CaO based adsorbent is widely applied in gas purification process especially at high temperature reaction. CaO is normally been produced via thermal decomposition of calcium carbonate (CaCO3 sources such as limestone which is obtained through mining and quarrying limestone hill. Yet, this study able to exploit the vast availability of waste resources in Malaysia which is cockle shell, as the potential biomass resources for CaCO3 and CaO. In addition, effect of particle size towards decomposition process is put under study using four particle sizes which are 0.125-0.25 mm, 0.25-0.5 mm, 1-2 mm, and 2-4 mm. Decomposition reactivity is conducted using Thermal Gravimetric Analyzer (TGA at heating rate of 20°C/minutes in inert (Nitrogen atmosphere. Chemical property analysis using x-ray fluorescence (XRF, shows cockle shell is made up of 97% Calcium (Ca element and CaO is produced after decomposition is conducted, as been analyzed by x-ray diffusivity (XRD analyzer. Besides, smallest particle size exhibits the highest decomposition rate and the process was observed to follow first order kinetics. Activation energy, E, of the process was found to vary from 179.38 to 232.67 kJ/mol. From Arrhenius plot, E increased when the particle size is larger. To conclude, cockle shell is a promising source for CaO and based on four different particles sizes used, sample at 0.125-0.25 mm offers the highest decomposition rate.

  5. Effects of nano calcium carbonate and nano calcium citrate on toxicity in ICR mice and on bone mineral density in an ovariectomized mice model

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Sherry; Chen, Jin Ching; Hsu, Chin Wei; Chang, Walter H, E-mail: whchang@cycu.edu.t [Center for Nano Bioengineering, Chung Yuan Christian University, Chung Li 32023, Taiwan (China); Department of Biomedical Engineering, Chung Yuan Christian University, Chung Li 32023, Taiwan (China)

    2009-09-16

    Taking calcium supplements can reduce the risk of developing osteoporosis, but they are not readily absorbed in the gastrointestinal tract. Nanotechnology is expected to resolve this problem. In the present study, we examined whether the bioavailability of calcium carbonate and calcium citrate can be improved by reducing the particle size. The morphology of nano calcium carbonate and nano calcium citrate was characterized by dynamic laser-light scattering (DLS), field-emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM). The measurements obtained from DLS, FE-SEM and TEM were comparable. Acute and sub-chronic toxicity tests were performed to establish the safety of these products after oral administration. The no-observed-adverse-effect levels of nano calcium carbonate and nano calcium citrate were 1.3 and 2.3 g kg{sup -1} body weight, respectively. The results of our in vivo studies indicate that administering nano calcium carbonate and nano calcium citrate can enhance the serum calcium concentration and maintain the whole-body bone mineral density in ovariectomized mice. These data suggest that nano calcium carbonate and nano calcium citrate are more bioavailable than micro calcium carbonate and micro calcium citrate, respectively.

  6. Effects of nano calcium carbonate and nano calcium citrate on toxicity in ICR mice and on bone mineral density in an ovariectomized mice model

    Science.gov (United States)

    Huang, Sherry; Chen, Jin Ching; Hsu, Chin Wei; Chang, Walter H.

    2009-09-01

    Taking calcium supplements can reduce the risk of developing osteoporosis, but they are not readily absorbed in the gastrointestinal tract. Nanotechnology is expected to resolve this problem. In the present study, we examined whether the bioavailability of calcium carbonate and calcium citrate can be improved by reducing the particle size. The morphology of nano calcium carbonate and nano calcium citrate was characterized by dynamic laser-light scattering (DLS), field-emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM). The measurements obtained from DLS, FE-SEM and TEM were comparable. Acute and sub-chronic toxicity tests were performed to establish the safety of these products after oral administration. The no-observed-adverse-effect levels of nano calcium carbonate and nano calcium citrate were 1.3 and 2.3 g kg-1 body weight, respectively. The results of our in vivo studies indicate that administering nano calcium carbonate and nano calcium citrate can enhance the serum calcium concentration and maintain the whole-body bone mineral density in ovariectomized mice. These data suggest that nano calcium carbonate and nano calcium citrate are more bioavailable than micro calcium carbonate and micro calcium citrate, respectively.

  7. Preparation of hardened body in calcium carbonate-aspartic acid-chitosan system by using amorphous calcium carbonate; Hishoshitsu tansan calcium wo genryo to suru tansan calcium-asuparaginsan-kitosankei kokatai no sakusei

    Energy Technology Data Exchange (ETDEWEB)

    Yasue, T.; Aigami, H.; Arai, Y. [Nihon University, Tokyo (Japan). Faculty of Science and Engineering

    1998-11-01

    Notice was given on chitosan to discuss fabrication of hardened body in calcium carbonate-aspartic acid-chitosan system. First, aspartic acid (Asp) was adsorbed into surface of amorphous calcium carbonate (ACC). Then, discussions were given on effects of water-solid mass ratio and chitosan amount on compressive strength of the hardened body in the calcium carbonate-chitosan system made by using a flow-in molding process. As a result, approximately the same compressive strength as that of calcium carbonate (calcite type) was obtained when anhydrous ACC as a product of ACC heated at 250 deg C is used as the raw material. Thus, the hardened body in calcium carbonate-aspartic acid-chitosan system was fabricated by using the Asp adsorbed anhydrous ACC as the starting material. The compressive strength decreased with increasing Asp adsorption amount. Therefore, a hardened body was fabricated by using compression molding at 10 MPa, rather than using the flow-in molding process. It was revealed from the results of infrared absorption spectroscopy that the compression molding strengthens the compounding of Asp chemically adsorbed on the ACC surface with chtosan, and improves the compression strength. 23 refs., 8 figs.

  8. Calcium carbonate nucleation in an alkaline lake surface water, Pyramid Lake, Nevada, USA

    Science.gov (United States)

    Reddy, Michael M.; Hoch, Anthony

    2012-01-01

    Calcium concentration and calcite supersaturation (Ω) needed for calcium carbonate nucleation and crystal growth in Pyramid Lake (PL) surface water were determined during August of 1997, 2000, and 2001. PL surface water has Ω values of 10-16. Notwithstanding high Ω, calcium carbonate growth did not occur on aragonite single crystals suspended PL surface water for several months. However, calcium solution addition to PL surface-water samples caused reproducible calcium carbonate mineral nucleation and crystal growth. Mean PL surface-water calcium concentration at nucleation was 2.33 mM (n = 10), a value about nine times higher than the ambient PL surface-water calcium concentration (0.26 mM); mean Ω at nucleation (109 with a standard deviation of 8) is about eight times the PL surface-water Ω. Calcium concentration and Ω regulated the calcium carbonate formation in PL nucleation experiments and surface water. Unfiltered samples nucleated at lower Ω than filtered samples. Calcium concentration and Ω at nucleation for experiments in the presence of added particles were within one standard deviation of the mean for all samples. Calcium carbonate formation rates followed a simple rate expression of the form, rate (mM/min) = A (Ω) + B. The best fit rate equation "Rate (Δ mM/Δ min) = -0.0026 Ω + 0.0175 (r = 0.904, n = 10)" was statistically significant at greater than the 0.01 confidence level and gives, after rearrangement, Ω at zero rate of 6.7. Nucleation in PL surface water and morphology of calcium carbonate particles formed in PL nucleation experiments and in PL surface-water samples suggest crystal growth inhibition by multiple substances present in PL surface water mediates PL calcium carbonate formation, but there is insufficient information to determine the chemical nature of all inhibitors.

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

    DEFF Research Database (Denmark)

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

    2016-01-01

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

  10. Calcium carbonate precipitation in the Cueva di Watapana on Bonaire, Netherlands Antilles

    NARCIS (Netherlands)

    Meer Mohr, van der C.G.

    1978-01-01

    Calcium carbonate precipitates as low Mg-calcite and aragonite in slightly brackish water in a cave in the Pleistocene Middle Terrace of southern Bonaire. The calcium carbonate precipitates at the atmosphere-water interface forming floating calcite scales (calcite ice). Aragonite crystals frequently

  11. Granule fraction inhomogeneity of calcium carbonate/sorbitol in roller compacted granules

    DEFF Research Database (Denmark)

    Bacher, Charlotte; Olsen, P.M.; Bertelsen, P.;

    2008-01-01

    The granule fraction inhomogeneity of roller compacted granules was examined on mixtures of three different morphologic forms of calcium carbonate and three particle sizes of sorbitol. The granule fraction inhomogeneity was determined by the distribution of the calcium carbonate in each of the 10...

  12. Formation of amorphous calcium carbonate in caves and its implications for speleothem research

    Science.gov (United States)

    Demény, Attila; Németh, Péter; Czuppon, György; Leél-Őssy, Szabolcs; Szabó, Máté; Judik, Katalin; Németh, Tibor; Stieber, József

    2016-12-01

    Speleothem deposits are among the most valuable continental formations in paleoclimate research, as they can be dated using absolute dating methods, and they also provide valuable climate proxies. However, alteration processes such as post-depositional mineralogical transformations can significantly influence the paleoclimatic application of their geochemical data. An innovative sampling and measurement protocol combined with scanning and transmission electron microscopy, X-ray diffraction and Fourier transform infrared spectroscopy is presented, demonstrating that carbonate precipitating from drip water in caves at ~10 °C contains amorphous calcium carbonate (ACC) that later transforms to nanocrystalline calcite. Stable oxygen isotope fractionations among calcite, ACC and water were also determined, proving that ACC is 18O-depleted (by >2.4 ± 0.8‰) relative to calcite. This, in turn, has serious consequences for speleothem-based fluid inclusion research as closed system transformation of ACC to calcite may induce a negative oxygen isotope shift in fluid inclusion water, resulting in deterioration of the original compositions. ACC formation increases the speleothems’ sensitivity to alteration as its interaction with external solutions may result in the partial loss of original proxy signals. Mineralogical analysis of freshly precipitating carbonate at the studied speleothem site is suggested in order to determine the potential influence of ACC formation.

  13. Link between the early calcium deposition in placenta and nanobaсterial-like infection

    Indian Academy of Sciences (India)

    R M Agababov; T N Abashina; N E Suzina; M B Vainshtein; P M Schwartsburd

    2007-09-01

    The placenta is a vitally important organ in the regulation of embryonic development. That is why extensive calcium deposition [also named as pathological placental calcification (PPC)] could have serious negative consequences for the adequate growth of embryos. The nature and mechanism of PPC development has not been defined as yet. In the present investigation, we have tested the hypothesis that the molecular basis of PPC development consists of nanobacteria-induced calcification in infected female placenta. Electron microscopy findings support this hypothesis. The initial stage of micro-calcification may originate from the external surface of individual nanobacteria-like particles found mainly in placental extracellular matrix, where initial calcium deposition occurs as a needle surface deposition or as an amorphous-like surface precipitate. Further calcific propagation in placenta takes place in the newly formed macro-cavities, which are characterized by low electron density, possibly reflecting its liquid content around calcium deposition. The micro-cavities contain free nanobacterial-like particles, which may relate to atypical Gram-negative bacteria but not to apoptotic bodies by morphological characters and DNA/RNA distribution. We hypothesize that the increased placental calcification might be caused, at least in part, by nanobacterial infection.

  14. High Energy Radial Deposition of Diamond-Like Carbon Coatings

    Directory of Open Access Journals (Sweden)

    Konrad Suschke

    2015-07-01

    Full Text Available Diamond-like carbon (DLC coatings were deposited with a new direct ion deposition system using a novel 360 degree ion source operating at acceleration voltage between 4 and 8 kV. Cross-sectional TEM images show that the coatings have a three layered structure which originates from changes in the deposition parameters taking into account ion source condition, ion current density, deposition angles, ion sputtering and ion source movement. Varying structural growth conditions can be achieved by tailoring the deposition parameters. The coatings show good promise for industrial use due to their high hardness, low friction and excellent adhesion to the surface of the samples.

  15. Heat mass transfer model of fouling process of calcium carbonate on heat transfer surface

    Institute of Scientific and Technical Information of China (English)

    QUAN ZhenHua; CHEN YongChang; MA ChongFang

    2008-01-01

    A new heat mass transfer model was developed to predict the fouling process of calcium carbonate on heat transfer surface.The model took into account not only the crystallization fouling but also the particle fouling which was formed on the heat transfer surface by the suspension particles of calcium carbonate in the su-persaturated solution.Based on experimental results of the fouling process,the deposition and removal rates of the mixing fouling were expressed.Furthermore,the coupling effect of temperature with the fouling process was considered in the physics model.As a result the fouling resistance varying with time was obtained to describe the fouling process and the prediction was compared with experimental data under same conditions.The results showed that the present model could give a good prediction of fouling process,and the deviation was less than 15% of the experimental data in most cases.The new model is credible to predict the fouling process.

  16. Influence of precursor solution parameters on chemical properties of calcium phosphate coatings prepared using Electrostatic Spray Deposition (ESD).

    NARCIS (Netherlands)

    Leeuwenburgh, S.C.G.; Wolke, J.G.C.; Schoonman, J.; Jansen, J.A.

    2004-01-01

    A novel coating technique, referred to as Electrostatic Spray Deposition (ESD), was used to deposit calcium phosphate (CaP) coatings with a variety of chemical properties. The relationship between the composition of the precursor solutions and the crystal and molecular structure of the deposited coa

  17. Magnesium and occluded water in calcium carbonate monohydrate

    Science.gov (United States)

    Dejehet, F.; Idrissi, S.; Debuys, R.

    1999-04-01

    Calcium carbonate monohydrate spherulites (˜102 μm diameter) with different magnesium contents were synthesized from artificial seawater. Stable spherulites are only obtained if [Mg]/[Ca] ≥ 1-1.3 in the mother solution. Spherulites are surrounded by a skin of ˜15 μm thickness, about 5 times richer in Mg2+ than the bulk and which play a protective role from the stability viewpoint. Etching and crushing experiments were performed which confirm i.a. that the isotropic CO3- and CO2- radicals are located in the occluded water surrounding the constituent crystallites of the spherulites. Des sphérules de carbonate de calcium monohydraté de ˜102 μm de diamètre avec des teneurs en magnésium différentes ont été synthétisées à partir d'eau de mer artificielle. Des sphérules stables ne sont obtenues que si [Mg]/[Ca] ≥ 1-1.3 dans la solution mère. Les sphérules sont entourées d'une peau de ˜15 μm d'épaisseur, à peu près 5 fois plus riche en Mg2+ que la masse et qui assure sa stabilité. Des expériences de décapage et de broyage ont confirmé e.a. que les radicaux isotropes CO3- et CO2- sont localisés dans l'eau occluse entourant les cristallites à l'intérieur des sphérules.

  18. Co-precipitation of dissolved organic matter by calcium carbonate in Pyramid Lake, Nevada

    Science.gov (United States)

    Leenheer, Jerry A.; Reddy, Michael M.

    2008-01-01

    Our previous research has demonstrated that dissolved organic matter (DOM) influences calcium carbonate mineral formation in surface and ground water. To better understand DOM mediation of carbonate precipitation and DOM co-precipitation and/or incorporation with carbonate minerals, we characterized the content and speciation of DOM in carbonate minerals and in the lake water of Pyramid Lake, Nevada, USA. A 400-gram block of precipitated calcium carbonate from the Pyramid Lake shore was dissolved in 8 liters of 10% acetic acid. Particulate matter not dissolved by acetic acid was removed by centrifugation. DOM from the carbonate rock was fractionated into nine portions using evaporation, dialysis, resin adsorption, and selective precipitations to remove acetic acid and inorganic constituents. The calcium carbonate rock contained 0.23% DOM by weight. This DOM was enriched in polycarboxylic proteinaceous acids and hydroxy-acids in comparison with the present lake water. DOM in lake water was composed of aliphatic, alicyclic polycarboxylic acids. These compound classes were found in previous studies to inhibit calcium carbonate precipitation. DOM fractions from the carbonate rock were 14C-age dated at about 3,100 to 3,500 years before present. The mechanism of DOM co-precipitation and/or physical incorporation in the calcium carbonate is believed to be due to formation of insoluble calcium complexes with polycarboxylic proteinaceous acids and hydroxy-acids that have moderately large stability constants at the alkaline pH of the lake. DOM co-precipitation with calcium carbonate and incorporation in precipitated carbonate minerals removes proteinaceous DOM, but nearly equivalent concentrations of neutral and acidic forms of organic nitrogen in DOM remain in solution. Calcium carbonate precipitation during lime softening pretreatment of drinking water may have practical applications for removal of proteinaceous disinfection by-product precursors.

  19. Microanalyses of the hydroxyl-poly-calcium sodium phosphate coatings produced by ion beam assisted deposition

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Thin calcium phosphate coatings on titanium alloy substrates wereprepared by Ar+ ion beam assisted deposition (IBAD) from hydroxyl-poly-calciumsodium phosphate (HPPA) target. The coatings were analyzed by XRD, FTIR, XPS.These analyses revealed that the as-deposited films were amorphous or no apparentcrystallinity. No distinct absorption band of the hydroxyl group was observed in FTIRspectra of the coatings but new absorption bands were presented for CO3-2. Thecalcium to phosphorous ratio of these coatings in different IBAD conditions variedfrom 0.46 to 3.36.

  20. Technological testing of calcium carbonate tablets for use in the treatment of renal osteodystrophy.

    Science.gov (United States)

    Dal Zotto, M; Ragazzi, E; Realdon, N; Dalla Fini, G

    1993-07-01

    Samples of calcium carbonate tablets produced by different manufacturers were subjected to various tests in order to evaluate tablet quality parameters, mostly indicative for calcium availability. Indications about tablet suitability for treatment of renal osteodystrophy in uremic patients were also tested. The disintegration test turned out to be the most useful in evaluating calcium carbonate availability from tablets. Samples from several manufacturers varied in their behaviour to disaggregation. The availability of calcium dissolved in gastric fluid and the extent of phosphorus binding appeared to depend on disintegration behaviour.

  1. Deposition and tribological behaviour of sputtered carbon hard coatings

    Energy Technology Data Exchange (ETDEWEB)

    Yang, S.; Camino, D.; Jones, A.H.S.; Teer, D.G. [Teer Coatings Ltd., Hartlebury (United Kingdom)

    2000-02-21

    The exceptional tribological properties of low deposition temperature sputtered carbon coatings (Graphit-iC coatings) have been recently reported. This paper describes the latest development of these coatings and particularly how, by an optimisation of the deposition parameters, it has been possible to obtain relative soft to very hard coatings with extremely low specific wear rates. The coatings have been deposited in a closed field unbalanced magnetron sputter ion plating (CFUBMSIP) installation. By applying the appropriate conditions of deposition, carbon coatings with hardness from 1500 to 4000 HV can be routinely deposited. Preliminary analytical results are presented in order to characterise such hard coatings: high-resolution transmission electron microscopy, scanning electron microscopy and X-ray diffraction analysis are some of the different techniques used for this work. Finally, a number of the applications are reported with tribological test results. (orig.)

  2. Plasma reactor for deposition of carbon nanowalls at atmospheric pressure

    Science.gov (United States)

    Dimitrov, Zh; Mitev, D.; Kiss'ovski, Zh

    2016-10-01

    In this study a novel plasma reactor for deposition of carbon nanowalls at atmospheric pressure is constructed and characterized. A low power microwave discharge is used as a plasma source and working gas of Ar/H2/CH4 gas mixture. The substrate is heated by plasma flame and its temperature is in the range 600-700 C. The chemical composition of the plasma and the gas mixture effect on the concentration of the various particles in the plasma is investigated by optical emission spectroscopy. The emission spectrum of the plasma jet in Ar/H2/CH4 mixture shows the presence of carbon (Swan band) and an intensive line of CH (388 nm), which are necessary species for deposition of carbon nanostructures. Additional voltage in the range from -20 V to -100 V is applied in order to ensure the vertical growth of graphene walls. Results of deposited carbon nanostructures on metal substrate are shown.

  3. Calcium carbonate production response to future ocean warming and acidification

    Directory of Open Access Journals (Sweden)

    A. J. Pinsonneault

    2012-06-01

    Full Text Available Anthropogenic carbon dioxide (CO2 emissions are acidifying the ocean, affecting calcification rates in pelagic organisms, and thereby modifying the oceanic carbon and alkalinity cycles. However, the responses of pelagic calcifying organisms to acidification vary widely between species, contributing uncertainty to predictions of atmospheric CO2 and the resulting climate change. At the same time, ocean warming caused by rising CO2 is expected to drive increased growth rates of all pelagic organisms, including calcifiers. It thus remains unclear whether anthropogenic CO2 emissions will ultimately increase or decrease pelagic calcification rates. Here, we assess the importance of this uncertainty by introducing a dependence of calcium carbonate (CaCO3 production on calcite saturation state (ΩCaCO3 in an intermediate complexity coupled carbon-climate model. In a series of model simulations, we examine the impact of several variants of this dependence on global ocean carbon cycling between 1800 and 3500 under two different CO2 emissions scenarios. Introducing a calcification-saturation state dependence has a significant effect on the vertical and surface horizontal alkalinity gradients, as well as on the removal of alkalinity from the ocean through CaCO3 burial. These changes result in an additional oceanic uptake of carbon when calcification depends on ΩCaCO3 (of up to 270 Pg C, compared to the case where calcification does not depend on acidification. In turn, this response causes a reduction of global surface air temperature of up to 0.4 °C in year 3500. Different versions of the model produced varying results, and narrowing this range of uncertainty will require better understanding of both temperature and acidification effects on pelagic calcifiers. Nevertheless, our results suggest that alkalinity observations can be used

  4. Calcium carbonate production response to future ocean warming and acidification

    Directory of Open Access Journals (Sweden)

    A. J. Pinsonneault

    2011-12-01

    Full Text Available Anthropogenic carbon dioxide (CO2 emissions are acidifying the ocean, affecting calcification rates in pelagic organisms and thereby modifying the oceanic alkalinity cycle. However, the responses of pelagic calcifying organisms to acidification vary widely between species, contributing uncertainty to predictions of atmospheric CO2 and the resulting climate change. Meanwhile, ocean warming caused by rising CO2 is expected to drive increased growth rates of all pelagic organisms, including calcifiers. It thus remains unclear whether anthropogenic CO2 will ultimately increase or decrease the globally-integrated pelagic calcification rate. Here, we assess the importance of this uncertainty by introducing a variable dependence of calcium carbonate (CaCO3 production on calcite saturation state (ΩCaCO3 in the University of Victoria Earth System Climate Model, an intermediate complexity coupled carbon-climate model. In a series of model simulations, we examine the impact of this parameterization on global ocean carbon cycling under two CO2 emissions scenarios, both integrated to the year 3500. The simulations show a significant sensitivity of the vertical and surface horizontal alkalinity gradients to the parameterization, as well as the removal of alkalinity from the ocean through CaCO3 burial. These sensitivities result in an additional oceanic uptake of carbon when calcification depends on ΩCaCO3 (of up to 13 % of total carbon emissions, compared to the case where calcification is insensitive to acidification. In turn, this response causes a reduction of global surface air temperature of up to 0.4 °C in year 3500, a 13 % reduction in the amplitude of warming. Narrowing these uncertainties will require better understanding of both temperature and acidification effects on pelagic calcifiers. Preliminary examination suggests that

  5. Inhibitory effect of Hydrex anti-scalant on calcium scale deposition from seawater under multiple-effect distillers' conditions

    Directory of Open Access Journals (Sweden)

    Aiman Eid Al-Rawajfeh

    2015-09-01

    Full Text Available In this work, the inhibitory effect of a commercial anti-scalant (Veolia Hydrex® 9209 on the calcium minerals of carbonate, sulfate and hydrocalumite (Ca/Al clay deposition from seawater has been investigated. Different concentration factors and anti-scalant doses were studied by analyzing the water hardness and turbidity. The inhibitory effect of the investigated anti-scalant was efficient even at lower concentrations. The percentage inhibition decreases with increasing the temperature and increases with increasing the dose/amount of the anti-scalant. The carbonate scale inhibition was >99% and 98–99% at 50 and 70 °C, respectively. The percentage inhibition of sulfate from hemihydrate was ranged from 80% to 87% for 2 and 8 ppm anti-scalant at 50 °C. The inhibition of Ca/Al hydrocalumite deposition increases from 70% to 90% upon increasing the dose from 3 to 5 ppm, respectively. A recommended useful dose of antiscalant for seawater is 5 ppm.

  6. Calcium Deposits in the Crayfish, Cherax quadricarinatus: Microstructure Versus Elemental Distribution.

    Science.gov (United States)

    Luquet, Gilles; Dauphin, Yannicke; Percot, Aline; Salomé, Murielle; Ziegler, Andreas; Fernández, Maria S; Arias, José L

    2016-02-01

    The crayfish Cherax quadricarinatus stores calcium ions, easily mobilizable after molting, for calcifying parts of the new exoskeleton. They are chiefly stored as amorphous calcium carbonate (ACC) during each premolt in a pair of gastroliths synthesized in the stomach wall. How calcium carbonate is stabilized in the amorphous state in such a biocomposite remains speculative. The knowledge of the microstructure at the nanometer level obtained by field emission scanning electron microscopy and atomic force microscopy combined with scanning electron microscopy energy-dispersive X-ray spectroscopy, micro-Raman and X-ray absorption near edge structure spectroscopy gave relevant information on the elaboration of such an ACC-stabilized biomineral. We observed nanogranules distributed along chitin-protein fibers and the aggregation of granules in thin layers. AFM confirmed the nanolevel structure, showing granules probably surrounded by an organic layer and also revealing a second level of aggregation as described for other crystalline biominerals. Raman analyses showed the presence of ACC, amorphous calcium phosphate, and calcite. Elemental analyses confirmed the presence of elements like Fe, Na, Mg, P, and S. P and S are heterogeneously distributed. P is present in both the mineral and organic phases of gastroliths. S seems present as sulfate (probably as sulfated sugars), sulfonate, sulfite, and sulfoxide groups and, in a lesser extent, as sulfur-containing amino acids.

  7. Iodine-to-calcium ratios in carbonates suggest a primary origin for the Precambrian Lomagundi and Shuram carbon isotope excursions

    Science.gov (United States)

    Hardisty, D. S.; Lu, Z.; Planavsky, N. J.; Osburn, M. R.; Bekker, A.; Lyons, T. W.

    2013-12-01

    Systematic increases in iodine-to-calcium ratios (I/Ca) in carbonates from both the Precambrian Lomagundi and Shuram carbonate carbon isotope (δ13Ccarb) excursion intervals suggest primary origins for these events. Iodate (IO3-), the oxidized iodine species, is the exclusive species incorporated into carbonates. The high redox sensitivity of IO3- to deoxygenation requires highly oxidizing fluids for IO3- production, making I/Ca in platform carbonates a simple indicator of the presence of oxidizing fluids in the surface ocean. Similarly, redox sensitivity makes the proxy host susceptible to diagenetic iodine loss during carbonate recrystallization in reducing pore fluids. Recent work has shown carbonates to experience near-complete iodine loss during dolomitization in the Permian, and work from our group evaluating modern and recent carbonates demonstrate the potential for diagenetic iodine loss during carbonate recrystallization. In some cases, however, such as meteoric aragonite-to-calcite transitions, oxidizing pore fluids have the potential to buffer IO3- concentrations, causing negligible alteration to primary I/Ca despite negative shifts in δ13Ccarb. These results highlight that diagenetic alterations to I/Ca and δ13Ccarb need not always be coupled, but importantly, no observed scenario promotes post-depositional addition of iodine to carbonates. This means that, independent of δ13Ccarb, systematic, stratigraphic increases in I/Ca ratios observed in the carbonate record are most easily interpreted as resulting from depositional controls such as surface ocean redox or shifts in the total marine iodine reservoir. From this, increasing I/Ca ratios coincident with rising and falling δ13Ccarb trends for the Paleoproterozic Lomagundi and Neoproterozoic Shuram events, respectively, support suggestions of a primary origin for the δ13Ccarb excursions. Significant increase in I/Ca in dolomites deposited during the Lomagundi excursion, rising from blank values in

  8. Calcium phosphate thin films synthesized by pulsed laser deposition: Physico-chemical characterization and in vitro cell response

    Energy Technology Data Exchange (ETDEWEB)

    Mihailescu, I.N. [National Institute for Lasers, Plasma and Radiation Physics, 77125 Bucharest-Magurele (Romania)]. E-mail: mihailes@ifin.nipne.ro; Torricelli, P. [Servizio di Chirurgia Sperimentale-Istituto di Ricerca Codivilla PuttiIOR, Bologna (Italy); Bigi, A. [Department of Chemistry ' G. Ciamician' , University of Bologna, 40126 Bologna (Italy); Mayer, I. [Department of Inorganic and Analytical Chemistry, Hebrew University of Jerusalem, 91904 Jerusalem (Israel); Iliescu, M. [Institute of Physics and Chemistry of Materials, 67037 Strasbourg (France); Werckmann, J. [Institute of Physics and Chemistry of Materials, 67037 Strasbourg (France); Socol, G. [National Institute for Lasers, Plasma and Radiation Physics, 77125 Bucharest-Magurele (Romania); Miroiu, F. [National Institute for Lasers, Plasma and Radiation Physics, 77125 Bucharest-Magurele (Romania); Cuisinier, F. [Institut National de la Sante et de la Recherche Medicale, 67085 Strasbourg (France); Elkaim, R. [Institut National de la Sante et de la Recherche Medicale, 67085 Strasbourg (France); Hildebrand, G. [IBA e.V., Department of Biomaterials, Rosenhof, D-37308 Heilbad Heiligenstadt (Germany)

    2005-07-30

    We review the progress made by us using pulsed laser deposition (PLD) of two bioactive calcium phosphates: octacalcium phosphate (OCP) and Mn doped carbonated hydroxyapatite (Mn-CHA). Coatings of these materials well suited for biomimetic medical prostheses and pivots were synthesized on titanium substrates with a pulsed KrF* UV laser source. The best deposition conditions for Mn-CHA thin films were 13 Pa O{sub 2}, 400 deg. C with post heat treatment of 6 h in air enriched with water vapours. The coatings are stoichiometric and crystalline. For OCP, deposition at 150 deg. C in 50 Pa water vapor atmosphere, post treated by 6 h annealing in hot flux of water vapours, resulted in stoichiometric, but poorly-crystallized films. Degradation tests show different behavior for the OCP and Mn-CHA coatings. In vitro cell growth shows excellent adherence and biocompatibility of osteoblasts and fibroblasts in both OCP and Mn-CHA coatings. Human osteoblasts display normal proliferation and viability, and good differentiation behaviour.

  9. Calcium carbonate corrosivity in an Alaskan inland sea

    Directory of Open Access Journals (Sweden)

    W. Evans

    2013-09-01

    Full Text Available Ocean acidification is the hydrogen ion increase caused by the oceanic uptake of anthropogenic CO2, and is a focal point in marine biogeochemistry, in part, because this chemical reaction reduces calcium carbonate (CaCO3 saturation states (Ω to levels that are corrosive (i.e. Ω ≤ 1 to shell-forming marine organisms. However, other processes can drive CaCO3 corrosivity; specifically, the addition of tidewater glacial melt. Carbonate system data collected in May and September from 2009 through 2012 in Prince William Sound (PWS, a semi-enclosed inland sea located on the south-central coast of Alaska that is ringed with fjords containing tidewater glaciers, reveal the unique impact of glacial melt on CaCO3 corrosivity. Initial limited sampling was expanded in September 2011 to span large portions of the western and central sound, and included two fjords proximal to tidewater glaciers: Icy Bay and Columbia Bay. The observed conditions in these fjords affected CaCO3 corrosivity in the upper water column (pCO2 well below atmospheric levels. CaCO3 corrosivity in glacial melt plumes is poorly reflected by pCO2 or pHT, indicating that either one of these carbonate parameters alone would fail to track Ω in PWS. The unique Ω and pCO2 conditions in the glacial melt plumes enhances atmospheric CO2 uptake, which, if not offset by mixing or primary productivity, would rapidly exacerbate CaCO3 corrosivity in a positive feedback. The cumulative effects of glacial melt and air-sea gas exchange are likely responsible for the seasonal widespread reduction of Ω in PWS; making PWS highly sensitive to increasing atmospheric CO2 and amplified CaCO3 corrosivity.

  10. Composition and source identification of deposits forming in landfill gas (LFG) engines and effect of activated carbon treatment on deposit composition.

    Science.gov (United States)

    Sevimoğlu, Orhan; Tansel, Berrin

    2013-10-15

    Compositions of deposits forming on engines parts operated with landfill gas (LFG) were analyzed. The deposit compositions were compared before and after the installation of activated carbon system for treatment of LFG. Deposits forming on the spark plugs had significantly higher levels of calcium, chromium, and nickel in comparison to those forming on the engine heads. The LFG contained about 9.5 ± 0.4 mg/m(3) total siloxanes, majority of which were octamethylcyclotetrasiloxane (D4) (5.0 ± 0.2 mg/m(3)), decamethylcyclopentasiloxane (D5) (2.9 ± 0.1 mg/m(3)) and hexamethyldisiloxane (L2) (1.6 ± 0.1 mg/m(3)). The samples collected from the engine heads before the activated carbon treatment of LFG had significantly high levels of silicon (149,400 ± 89,900 mg/kg) as well as calcium (70,840 ± 17,750 mg/kg), sulfur (42,500 ± 11,500 mg/kg), and zinc (22,300 ± 7200 mg/kg). After the activated carbon treatment, silicon levels decreased significantly; however, deposits had higher sulfur content (104,560 ± 68,100 mg/kg) indicating that the activated carbon released some sulfur during treatment. The analyses indicate that zinc and calcium originated from the additives in the lube oil while lead, aluminum, copper, nickel, iron, chromium were due to the engine wear.

  11. Mechanisms for the removal of calcium phosphate deposits in turbulent flow

    Energy Technology Data Exchange (ETDEWEB)

    Littlejohn, F.; Grant, C.S.; Saez, A.E.

    2000-04-01

    This work investigates the mechanisms for the removal of calcium phosphate deposits from stainless steel tubing in turbulent flows. Two types of deposits were analyzed: brushite (dicalcium phosphate dihydrate, DCPD) and a mixture of DCPD/hydroxyapatite (HAP). Cleaning studies were carried out at pHs ranging from 2.85 to 10. The data were analyzed by means of a mathematical model that incorporates the effects of interfacial dissolution and mass transfer. The results show that the HAP/DCPD cleaning rate is influenced both by the kinetics of the interfacial dissolution and by mass transfer. Within the same range of experimental conditions, the rate-limiting mechanism for DCPD removal was the abrasion of the solid by shear stresses. In this case, the interfacial dissolution process plays the role of decreasing the structural integrity of the deposit. These findings show that the removal mechanism of the HAP/DCPD mixture differs significantly from the behavior of individual components.

  12. Evidence for change in depositional environment in the Arabian Sea

    Digital Repository Service at National Institute of Oceanography (India)

    Rao, P.S.; Rao, Ch.M.

    cm interval were analyzed for calcium carbonate, organic carbon and reduced sulfur contents. Sedimentological analysis indicates that the core contains hemipelagic Globigerina ooze of Holocene age at the top, underlain by sediments depositEd...

  13. Effect of calcium carbonate combined with calcitonin on hypercalcemia in hemodialysis patients.

    Science.gov (United States)

    Wei, Yong; Kong, Xiang Lei; Li, Wen Bin; Wang, Zun Song

    2014-12-01

    This short-term study assessed the efficacy and safety of calcium carbonate combined with calcitonin in the treatment of hypercalcemia in hemodialysis patients. Patients (n=64) on hemodialysis for chronic kidney disease for more than 6 months were included based on total serum calcium more than 10.5 mg/dL. All patients were randomized (1:1) to receive calcium carbonate combined with calcitonin (Group I) or lanthanum carbonate (Group II) for 12 weeks. Blood levels of calcium, phosphorus and intact parathyroid hormone (iPTH) were measured every month, bone mass density (BMD) and coronary artery calcium scores (CACS) were measured at 3 months. During the study period, serum calcium decreased from 10.72 ± 0.39 to 10.09 ± 0.28 mg/dL (P carbonate combined with calcitonin and lanthanum carbonate were equally effective in the suppression of hypercalcemia in hemodialysis patients. There were no serious treatment-related adverse events in treatment with calcium carbonate combined with calcitonin.

  14. Crystallization kinetics of calcium carbonate at a stoichiometric ratio of components

    Science.gov (United States)

    Pochitalkina, I. A.; Kekin, P. A.; Morozov, A. N.; Petropavlovskii, I. A.; Kondakov, D. F.

    2016-12-01

    The formal kinetics of calcium carbonate crystallization in aqueous solutions is studied at a stoichiometric ratio of Ca2+ and CO3 2- ions. The kinetics of the process was monitored by convenient and reliable methods (complexometric analysis for calcium in an aqueous solution and energy dispersive and microscopic measurement of solid particle sizes). The effect the temperature and degree of supersaturation have on the periods of induction and mass crystallization and the equilibrium concentration of calcium ions in solution is estimated at continuously controlled pH and solution ionic strength. The kinetic parameters ( n, k, τ1/2, E a) of calcium carbonate crystallization are calculated. It is shown that calcium carbonate with a calcite structure formed at a stoichiometric ratio of reagents, and changes in the temperature (25-45°C) and the solution's degree of supersaturation (2-6) within the considered range had no effect on the characteristics of the solid phase.

  15. Increasing the Tensile Property of Unidirectional Carbon/Carbon Composites by Grafting Carbon Nanotubes onto Carbon Fibers by Electrophoretic Deposition

    Institute of Scientific and Technical Information of China (English)

    Qiang Song; Kezhi Li; Hejun Li; Qiangang Fu

    2013-01-01

    Although in-situ growing carbon nanotubes (CNTs) on carbon fibers could greatly increase the matrix-dominated mechanical properties of carbon/carbon composites (C/Cs),it always decreased the tensile strength of carbon fibers.In this work,CNTs were introduced into unidirectional carbon fiber (CF) preforms by electrophoretic deposition (EPD) and they were used to reinforce C/Cs.Effects of the content of CNTs introduced by EPD on tensile property of unidirectional C/Cs were investigated.Results demonstrated that EPD could be used as a simple and efficient method to fabricate carbon nanotube reinforced C/Cs (CNT-C/Cs) with excellent tensile strength,which pays a meaningful way to maximize the global performance of CNT-C/Cs.

  16. [Microbial geochemical calcium cycle].

    Science.gov (United States)

    Zavarzin, G A

    2002-01-01

    The participation of microorganisms in the geochemical calcium cycle is the most important factor maintaining neutral conditions on the Earth. This cycle has profound influence on the fate of inorganic carbon, and, thereby, on the removal of CO2 from the atmosphere. The major part of calcium deposits was formed in the Precambrian, when prokaryotic biosphere predominated. After that, calcium recycling based on biogenic deposition by skeletal organisms became the main process. Among prokaryotes, only a few representatives, e.g., cyanobacteria, exhibit a special calcium function. The geochemical calcium cycle is made possible by the universal features of bacteria involved in biologically mediated reactions and is determined by the activities of microbial communities. In the prokaryotic system, the calcium cycle begins with the leaching of igneous rock predominantly through the action of the community of organotrophic organisms. The release of carbon dioxide to the soil air by organotrophic aerobes leads to leaching with carbonic acid and soda salinization. Under anoxic conditions, of major importance is the organic acid production by primary anaerobes (fermentative microorganisms). Calcium carbonate is precipitated by secondary anaerobes (sulfate reducers) and to a smaller degree by methanogens. The role of the cyanobacterial community in carbonate deposition is exposed by stromatolites, which are the most common organo-sedimentary Precambrian structures. Deposition of carbonates in cyanobacterial mats as a consequence of photoassimilation of CO2 does not appear to be a significant process. It is argued that carbonates were deposited at the boundary between the "soda continent", which emerged as a result of subaerial leaching with carbonic acid, and the ocean containing Ca2+. Such ecotones provided favorable conditions for the development of the benthic cyanobacterial community, which was a precursor of stromatolites.

  17. Polymer surface modification and characterization of particulate calcium carbonate fillers

    Energy Technology Data Exchange (ETDEWEB)

    Shui Miao

    2003-12-30

    The efficacy of the surface treatment of particulate fillers depends on the chemical character of the components, on the method and conditions of the treatment, and on the amount of the treating agent. Here, the ultra-fine calcium carbonate is surface treated with 1, 2, 3 and 4 wt.% polyacrylic acid (PAA) synthesized by ourselves, which has strong ionic interaction and is an efficient surface modifier. The PAA coated filler is submitted to the measurement of the surface bonded amount, bonding efficacy, X-ray photoelectron spectroscopy (XPS) and inverse gas chromatography. Maximum efficacy is expected at the monolayer coverage of the surface, which is about 0.6 wt.% according to the calculation based on the way they are aligned and is basically in agreement with the 'substrate overlayer' model based on the mole ratio of C{sup 286} and C{sup 290} taking no account of the possible underestimation because of the inaccuracy or because of the CH{sub x} contamination present originally on the CaCO{sub 3}. The initial decrease of the mole ratio of C{sup 290}/O and C{sup 290}/Ca with the surface bonded PAA may indicate that the bonding interaction between the polymer and the filler surface is the leaving of one molecular carbon dioxide. The IGC measurement shows that there is a considerable surface tension falling in the case of the PAA modified filler compared with the reference. An abnormal high surface energy in the case of filler treated with 4% PAA is observed.

  18. Catalyst deposition for the preparation of carbon nanotubes

    DEFF Research Database (Denmark)

    2013-01-01

    Disclosed is a method of depositing islands of catalyst with a predetermined density, wherein in said method comprises the steps of: obtaining a diffusion barrier covered nano patterned surface comprising a plurality of plateaus, having a density of plateaus dependent on the predetermined density...... patterned surface is configured to ensure that no more than a single island of catalyst is formed on each plateau, so that a sub sequent growth of carbon nanotubes from the deposited islands result in that no more than a single carbon nanotube is grown from each plateau....

  19. Plasma Processes : Microwave plasma deposition of diamond like carbon coatings

    Indian Academy of Sciences (India)

    D S Patil; K Ramachandran; N Venkatramani; M Pandey; R D'Cunha

    2000-11-01

    The promising applications of the microwave plasmas have been appearing in the fields of chemical processes and semiconductor manufacturing. Applications include surface deposition of all types including diamond/diamond like carbon (DLC) coatings, etching of semiconductors, promotion of organic reactions, etching of polymers to improve bonding of the other materials etc. With a 2.45 GHz, 700 W, microwave induced plasma chemical vapor deposition (CVD) system set up in our laboratory we have deposited diamond like carbon coatings. The microwave plasma generation was effected using a wave guide single mode applicator. We have deposited DLC coatings on the substrates like stainless steel, Cu–Be, Cu and Si. The deposited coatings have been characterized by FTIR, Raman spectroscopy and ellipsometric techniques. The results show that we have achieved depositing ∼ 95% sp3 bonded carbon in the films. The films are uniform with golden yellow color. The films are found to be excellent insulators. The ellipsometric measurements of optical constant on silicon substrates indicate that the films are transparent above 900 nm.

  20. Diffusion-reaction compromise the polymorphs of precipitated calcium carbonate

    Institute of Scientific and Technical Information of China (English)

    Han Wang; Wenlai Huang; Yongsheng Han

    2013-01-01

    Diffusion is seldom considered by chemists and materialists in the preparation of materials while it plays an important role in the field of chemical engineering.If we look at crystallization at the atomic level,crystal growth in a solution starts from the diffusion of ions to the growing surface followed by the incorporation of ions into its lattice.Diffusion can be a rate determining step for the growth of crystals.In this paper,we take the crystallization of calcium carbonate as an example to illustrate the microscopic processes of diffusion and reaction and their compromising influence on the morphology of the crystals produced.The diffusion effect is studied in a specially designed three-cell reactor.Experiments show that a decrease of diffusion leads to retardation of supersaturation and the formation of a continuous concentration gradient in the reaction cell,thus promoting the formation of cubic calcite particles.The reaction rate is regulated by temperature.Increase of reaction rate favors the formation of needle-like aragonite particles.When diffusion and reaction play joint roles in the reaction system,their compromise dominates the formation of products,leading to a mixture of cubic and needle-like particles with a controllable ratio.Since diffusion and reaction are universal factors in the preparation of materials,the finding of this paper could be helpful in the controlled synthesis of other materials.

  1. Facile Synthesis of Calcium Carbonate Nanoparticles from Cockle Shells

    Directory of Open Access Journals (Sweden)

    Kh. Nurul Islam

    2012-01-01

    Full Text Available A simple and low-cost method for the synthesis of calcium carbonate nanoparticles from cockle shells was described. Polymorphically, the synthesized nanoparticles were aragonites which are biocompatible and thus frequently used in the repair of fractured bone and development of advanced drug delivery systems, tissue scaffolds and anticarcinogenic drugs. The rod-shaped and pure aragonite particles of 30±5 nm in diameter were reproducibly synthesized when micron-sized cockle shells powders were mechanically stirred for 90 min at room temperature in presence of a nontoxic and nonhazardous biomineralization catalyst, dodecyl dimethyl betaine (BS-12. The findings were verified using a combination of analytical techniques such as variable pressure scanning electron microscopy (VPSEM, transmission electron microscopy (TEM, Fourier transmission infrared spectroscopy (FT-IR, X-ray diffraction spectroscopy (XRD, and energy dispersive X-ray analyser (EDX. The reproducibility and low cost of the method suggested that it could be used in industry for the large scale synthesis of aragonite nanoparticles from cockle shells, a low cost and easily available natural resource.

  2. Biomaterial-Derived Calcium Carbonate Nanoparticles for Enteric Drug Delivery

    Directory of Open Access Journals (Sweden)

    Diane Render

    2016-01-01

    Full Text Available Oral drug delivery systems provide the most convenient, noninvasive, readily acceptable alternatives to parenteral systems. In the current work, eggshell-derived calcium carbonate (CaCO3 nanoparticles were used to develop enteric drug delivery system in the form of tablets. CaCO3 nanoparticles were manufactured using top-down ball-milling method and characterized by X-ray diffractometry (XRD and transmission electron microscopy (TEM and loaded with 5-fluorouracil as a model drug. Tablets with varying CaCO3 core and binder compositions were fabricated and coated with Eudragit S100 or Eudragit L100. Suitability for enteric delivery of the tablets was tested by oral administration to rabbits and radiography. Radiograph images showed that the tablet remained in the stomach of the rabbit for up to 3 hours. Further modifications of these biomaterial-derived nanoparticles and the coatings will enable manufacturing of stable formulations for slow or controlled release of pharmaceuticals for enteric delivery.

  3. Pacific Remote Islands MNM: Initial Survey Instructions for Calcium Carbonate Accretion

    Data.gov (United States)

    US Fish and Wildlife Service, Department of the Interior — The purpose of the survey is to quantify the rate of calcium carbonate accretion to the coral reef benthos and to examine spatial and temporal variability in...

  4. Weight Percentage of Calcium Carbonate for 17 Equatorial Pacific Cores from Brown University

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Weight percentages of calcium carbonate in this file were compiled by J. Farrell and W. L. Prell of Brown University for 17 equatorial Pacific Ocean sediment cores....

  5. Synthesis of Aligned Carbon Nanotubes by Thermal Chemical Vapor Deposition

    Institute of Scientific and Technical Information of China (English)

    LI Gang; ZHOU Ming; MA Weiwei; CAI Lan

    2009-01-01

    Single crystal silicon was found to be very beneficial to the growth of aligned carbon nanotubes by chemical vapor deposition with C2H2 as carbon source. A thin film of Ni served as catalyst was deposited on the Si substrate by the K575X Peltier Cooled High Resolution Sputter Coater before growth. The growth properties of carbon nanotubes were studied as a function of the Ni catalyst layer thickness. The diameter, growth rate and areal density of the carbon nanotubes were controlled by the initial thickness of the catalyst layer. Steric hindrance between nanotubes forces them to grow in well-aligned manner at an initial stage of growth. Transmission electron microscope analysis revealed that nanotubes grew by a tip growth mechanism.

  6. Hardness and stress of amorphous carbon film deposited by glow discharge and ion beam assisting deposition

    CERN Document Server

    Marques, F C

    2000-01-01

    The hardness and stress of amorphous carbon films prepared by glow discharge and by ion beam assisting deposition are investigated. Relatively hard and almost stress free amorphous carbon films were deposited by the glow discharge technique. On the other hand, by using the ion beam assisting deposition, hard films were also obtained with a stress of the same order of those found in tetrahedral amorphous carbon films. A structural analysis indicates that all films are composed of a sp sup 2 -rich network. These results contradict the currently accepted concept that both stress and hardness are only related to the concentration of sp sup 3 sites. Furthermore, the same results also indicate that the sp sup 2 sites may also contribute to the hardness of the films.

  7. Nucleation and electrolytic deposition of lead on model carbon electrodes

    Science.gov (United States)

    Cericola, D.; Spahr, M.

    2016-08-01

    There is a general consensus in the lead acid battery industry for the use of carbon additives as a functional component in the negative paste to boost the battery performance with regards to charge acceptance and cycle life especially for upcoming automotive and energy storage applications. Several mechanisms are discussed in the scientific literature and the affinity of the carbon surfaces to lead species seems to play a key role. With a set of experiments on model carbon electrodes we gave evidence to the fact that some carbon materials promote spontaneous nucleation of lead crystals. We propose a mechanism such that the carbon, as soon as in a lead containing environment, immobilizes some lead on its surface. Such immobilized lead acts as nucleation seed for the deposition of lead when a current is passed through the material. It is therefore possible to differentiate and select the carbon materials based on their ability to form nucleation seeds.

  8. Effects of aluminum hydroxide and calcium carbonate antacids on the bioavailability of ciprofloxacin.

    OpenAIRE

    Frost, R W; Lasseter, K C; Noe, A J; Shamblen, E C; Lettieri, J T

    1992-01-01

    This study was designed to determine the effects of an aluminum hydroxide antacid and a calcium carbonate antacid on the bioavailability of ciprofloxacin (Cipro). Cipro (750 mg) was administered orally to 12 healthy volunteers in a three-way randomized crossover design. The three treatments included Cipro alone, four 850-mg calcium carbonate tablets taken 5 min before Cipro, and three 600-mg aluminum hydroxide tablets taken 5 min before Cipro. The relative bioavailability of Cipro when given ...

  9. Atmospheric Plasma Deposition of Diamond-like Carbon Coatings

    Energy Technology Data Exchange (ETDEWEB)

    Ladwig, Angela

    2008-01-23

    There is great demand for thin functional coatings in the semiconductor, optics, electronics, medical, automotive and aerospace industries [1-13]. As fabricated components become smaller and more complex, the properties of the materials’ surface take on greater importance. Thin coatings play a key role in tailoring surfaces to give them the desired hardness, wear resistance, chemical inertness, and electrical characteristics. Diamond-like carbon (DLC) coatings possess an array of desirable properties, including outstanding abrasion and wear resistance, chemical inertness, hardness, a low coefficient of friction and exceptionally high dielectric strength [14-22]. Diamond-like carbon is considered to be an amorphous material, containing a mixture of sp2 and sp3 bonded carbon. Based on the percentage of sp3 carbon and the hydrogen content, four different types of DLC coatings have been identified: tetrahedral carbon (ta-C), hydrogenated amorphous carbon (a-C:H) hard, a-C:H soft, and hydrogenated tetrahedral carbon (ta-C:H) [20,24,25]. Possessing the highest hardness of 80 GPa, ta-C possesses an sp3 carbon content of 80 to 88u%, and no appreciable hydrogen content whereas a-C:H soft possesses a hardness of less than 10 GPa, contains an sp3 carbon content of 60% and a hydrogen content between 30 to 50%. Methods used to deposit DLC coatings include ion beam deposition, cathodic arc spray, pulsed laser ablation, argon ion sputtering, and plasma-enhanced chemical vapor deposition [73-83]. Researchers contend that several advantages exist when depositing DLC coatings in a low-pressure environment. For example, ion beam processes are widely utilized since the ion bombardment is thought to promote denser sp3-bonded carbon networks. Other processes, such as sputtering, are better suited for coating large parts [29,30,44]. However, the deposition of DLC in a vacuum system has several disadvantages, including high equipment cost and restrictions on the size and shape of

  10. Nacre-like calcium carbonate controlled by ionic liquid/graphene oxide composite template

    Energy Technology Data Exchange (ETDEWEB)

    Yao, Chengli [School of Chemistry and Chemical Engineering, Anhui University, Hefei, Anhui 230039 (China); School of Chemistry and Chemical Engineering, Hefei Normal University, Hefei, Anhui 230601 (China); Xie, Anjian, E-mail: anjx@163.com [School of Chemistry and Chemical Engineering, Anhui University, Hefei, Anhui 230039 (China); Shen, Yuhua [School of Chemistry and Chemical Engineering, Anhui University, Hefei, Anhui 230039 (China); Zhu, Jinmiao; Li, Hongying [School of Chemistry and Chemical Engineering, Hefei Normal University, Hefei, Anhui 230601 (China)

    2015-06-01

    Nacre-like calcium carbonate nanostructures have been mediated by an ionic liquid (IL)-graphene oxide (GO) composite template. The resultant crystals were characterized by scanning electron microscopy (SEM), Fourier transform infrared (FT-IR) spectroscopy, and X-ray powder diffractometry (XRD). The results showed that either 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIM]BF{sub 4}) or graphene oxide can act as a soft template for calcium carbonate formation with unusual morphologies. Based on the time-dependent morphology changes of calcium carbonate particles, it is concluded that nacre-like calcium carbonate nanostructures can be formed gradually utilizing [BMIM]BF{sub 4}/GO composite template. During the process of calcium carbonate formation, [BMIM]BF{sub 4} acted not only as solvents but also as morphology templates for the fabrication of calcium carbonate materials with nacre-like morphology. Based on the observations, the possible mechanisms were also discussed. - Highlights: • Nacre-like CaCO{sub 3}/GO were prepared by gas diffusion. • Ionic liquid/GO served as composite templates. • The interaction of Ca{sup 2+} ions and GO played a very important role in the formation of nacre-like CaCO{sub 3}.

  11. Biologically formed calcium carbonate, a durable plugging agent for enhanced oil recovery

    Energy Technology Data Exchange (ETDEWEB)

    Nemati, M. [University of Saskatchewan, Dept. of Chemical Engineering, Saskatoon, SK (Canada); Voordouw, G. [University of Calgary, Dept. of Biological Sciences, Calgary, AB (Canada)

    2004-02-01

    The use of bacterially precipitated inorganic compounds such as calcium carbonate and silica have been suggested as an effective method for selective plugging of reservoirs as a means to improve microscopic and volumetric sweep efficiencies within a given geological formation. In this paper controlled enzymatic and bacterial formation of calcium carbonate were studied using a purified urease enzyme and a bacterium isolated from a Canadian oil field. Results showed that the quantity of produced calcium carbonate in the presence of bacteria was dependent on urea concentration. The highest amount achieved was 15 g/L urea. Enzymatically, the maximum concentration of calcium carbonate was 2.6 times higher than that achieved in the presence of bacteria (57.6 g/L vs 21.5 g/L). The production of calcium carbonate appeared to be less sensitive to temperature in the presence of bacteria, whereas production rates were enhanced with the urease enzyme as the temperature was increased from 20 degrees C to 50 degrees C. Plugging studies in unconsolidated porous media and in a core-flooding system with Beria sandstone indicated that in situ formation of calcium carbonate could effectively decrease the permeability of the porous media. Nevertheless, it should be noted that plugging by biomass is not permanent, and permeabilities will increase as degradation of bacterial cells progresses. 5 refs., 4 tabs., 1 fig.

  12. Green Synthesis of Calcium Carbonate Uniform Microspheres Using Vegetables%Green Synthesis of Calcium Carbonate Uniform Microspheres Using Vegetables

    Institute of Scientific and Technical Information of China (English)

    Chen, Long; Bao, Zuben; Pan, Jian; Xu, Weibing; Zhang, Heping; Hu, Hongbo; Hu, Jichao; Zhou, Lili

    2012-01-01

    We report a novel strategy for the green synthesis of calcium carbonate (CaCO3) microspheres by using four vegetables: potato, cucumber, aubergine, and carrot. The products were characterized by scanning electron microscopy, X-ray powder diffractometry and/or Fourier transform infrared spectroscopy. The results show that the spherical calcite crystals are obtained in the presence of potato, cucumber and aubergine extracts, while uniform vaterite and calcite mixed microspheres are produced with the extracts of carrot. The possible formation mechanism of the CaCO3 microspheres by using vegetables is also discussed, suggesting that the biomolecules especially proteins may induce and control the nucleation and growth of CaCO3 crystals. CaCO3 is an important biomineral and inorganic material. Uniform particles have numerous important applications in many areas. Therefore, this study is very significant not only for expanding the scope of crystal engineering, but also for biomineralization research and green synthesis of functional inorganic materials.

  13. Strangelove Ocean and Deposition of Unusual Shallow-Water Carbonates After the End-Permian Mass Extinction

    Science.gov (United States)

    Rampino, Michael R.; Caldeira, Ken

    2003-01-01

    The severe mass extinction of marine and terrestrial organisms at the end of the Permian Period (approx. 251 Ma) was accompanied by a rapid negative excursion of approx. 3 to 4 per mil in the carbon-isotope ratio of the global surface oceans and atmosphere that persisted for some 500,000 into the Early Triassic. Simulations with an ocean-atmosphere/carbon-cycle model suggest that the isotope excursion can be explained by collapse of ocean primary productivity (a Strangelove Ocean) and changes in the delivery and cycling of carbon in the ocean and on land. Model results also suggest that perturbations of the global carbon cycle resulting from the extinctions led to short-term fluctuations in atmospheric pCO2 and ocean carbonate deposition, and to a long-term (>1 Ma) decrease in sedimentary burial of organic carbon in the Triassic. Deposition of calcium carbonate is a major sink of river-derived ocean alkalinity and for CO2 from the ocean/atmosphere system. The end of the Permian was marked by extinction of most calcium carbonate secreting organisms. Therefore, the reduction of carbonate accumulation made the oceans vulnerable to a build-up of alkalinity and related fluctuations in atmospheric CO2. Our model results suggest that an increase in ocean carbonate-ion concentration should cause increased carbonate accumulation rates in shallow-water settings. After the end-Permian extinctions, early Triassic shallow-water sediments show an abundance of abiogenic and microbial carbonates that removed CaCO3 from the ocean and may have prevented a full 'ocean-alkalinity crisis' from developing.

  14. Compactibility of mixtures of calcium carbonate and microcrystalline cellulose.

    Science.gov (United States)

    Garzón, M de Lourdes; Villafuerte, Leopoldo

    2002-01-01

    A patented coprocessed mixture of microcrystalline cellulose (MC) and calcium carbonate (CC) is claimed to perform, as a pharmaceutical excipient, equal or better than pure MC. To investigate it, the tensile strength (T) of tablets made of mixtures of MC type 102, CC, magnesium stearate (MS) and polyvinylpyrrolidone (PVP) and formed under a compaction pressure (P(c)) ranging up to 618 MPa has been determined. The compactibility of the mixtures was defined through regression parameters obtained with ln(-ln(1-T/T(max)))=slope x lnP(c) + intercept. MC/CC mixtures, P(c)=618 MPa, show a small decrease in tablet tensile strength with CC proportions up to about 20%, falling considerably thereafter. Lower compaction pressures, P(c)tablet tensile strength due to 2%-MS, P(c)=487 MPa, was recovered to 35% of its original value admixing about 25% CC. This maximal value of recovery showed a shift to lower proportions of CC, up to 10%, as compaction pressure decreased. This was attributed to lower CC-particles fragmentation or agglomerates spreading at lower compaction pressures. Mixtures with increased plasticity (MC/CC/PVP and MC/CC/PVP/MS) showed an increased compactibility, which was more evident at higher compaction pressures and higher CC proportions, presumably due to higher deformation and erosion of PVP particles. Inclusion of about 40% CC in a MC/PVP/MS mixture showed 60% recovery of the original MC tablet tensile strength. Lower MS proportions are expected to allow a higher recovery.

  15. Characterization of calcium carbonate sorbent particle in furnace environment

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Kang Soo [Aerosol and Particle Technology Laboratory, Department of Mechanical Engineering, KAIST 291 Daehak-ro, Yuseong-gu, Daejeon, 305-701 (Korea, Republic of); Jung, Jae Hee [Environment Sensor System Research Center, KIST 39-1 Hawolgok-dong, Seongbuk-gu, Seoul, 136-791 (Korea, Republic of); Keel, Sang In; Yun, Jin Han; Min, Tai Jin [Environmental Systems Research Division, KIMM 104 Sinseongno, Yuseong-gu, Daejeon, 305-343 (Korea, Republic of); Kim, Sang Soo, E-mail: sskim@kaist.ac.kr [Aerosol and Particle Technology Laboratory, Department of Mechanical Engineering, KAIST 291 Daehak-ro, Yuseong-gu, Daejeon, 305-701 (Korea, Republic of)

    2012-07-01

    The oxy-fuel combustion system is a promising technology to control CO{sub 2} and NO{sub X} emissions. Furthermore, sulfation reaction mechanism under CO{sub 2}-rich atmospheric condition in a furnace may lead to in-furnace desulfurization. In the present study, we evaluated characteristics of calcium carbonate (CaCO{sub 3}) sorbent particles under different atmospheric conditions. To examine the physical/chemical characteristics of CaCO{sub 3}, which is used as a sorbent particle for in-furnace desulfurization in the oxy-fuel combustion system, they were injected into high temperature drop tube furnace (DTF). Experiments were conducted at varying temperatures, residence times, and atmospheric conditions in a reactor. To evaluate the aerosolizing characteristics of the CaCO{sub 3} sorbent particle, changes in the size distribution and total particle concentration between the DTF inlet and outlet were measured. Structural changes (e.g., porosity, grain size, and morphology) of the calcined sorbent particles were estimated by BET/BJH, XRD, and SEM analyses. It was shown that sorbent particles rapidly calcined and sintered in the air atmosphere, whereas calcination was delayed in the CO{sub 2} atmosphere due to the higher CO{sub 2} partial pressure. Instead, the sintering effect was dominant in the CO{sub 2} atmosphere early in the reaction. Based on the SEM images, it was shown that the reactions of sorbent particles could be explained as a grain-subgrain structure model in both the air and CO{sub 2} atmospheres.

  16. Soil Organic Carbon Stocks in Depositional Landscapes of Bavaria

    Science.gov (United States)

    Kriegs, Stefanie; Schwindt, Daniel; Völkel, Jörg; Kögel-Knabner, Ingrid

    2016-04-01

    Erosion leads to redistribution and accumulation of soil organic matter (SOM) within agricultural landscapes. These fluvic and colluvic deposits are characterized by a highly diverse vertical structure and can contain high amounts of soil organic carbon (SOC) over the whole soil profile. Depositional landscapes are therefore not only productive sites for agricultural use but also influence carbon dynamics which is of great interest with regard on the recent climate change debate. The aim of our study is to elucidate the spatial distribution of organic carbon stocks, as well as its depth function and the role of these landscapes as a reservoir for SOM. Therefore we compare two representative depositional landscapes in Bavaria composed of different parent materials (carbonate vs. granitic). We hypothesize that the soils associated with different depositional processes (fluvial vs. colluvial) differ in SOC contents and stocks, also because of different hydromorphic regimes in fluvic versus colluvic soil profiles. Sampling sites are located in the Alpine Foreland (quaternary moraines with carbonatic parent material) and the foothills of the Bavarian Forest (Granite with Loess) with the main soil types Fluvisols, Gleysols and Luvisols. At both sites we sampled twelve soil profiles up to 150 cm depth, six in the floodplain and six along a vertical slope transect. We took undisturbed soil samples from each horizon and analyzed them for bulk density, total Carbon (OC and IC) and total Nitrogen (N) concentrations. This approach allows to calculate total OC contents and OC stocks and to investigate vertical and horizontal distribution of OC stocks. It will also reveal differences in OC stocks due to the location of the soil profile in fluvic or colluvic deposition scenarios.

  17. Calcium-phosphate deposits on a hydrophilic acrylic intraocular lens after silicon oil tamponade

    Directory of Open Access Journals (Sweden)

    Rashid Alsaeidi

    2008-01-01

    Full Text Available We report a 52-year-old man who underwent uncomplicated cataract operation and posterior chamber lens implantation (hydrophilic acrylic lens in his left eye 5 years prior to presentation. Two years after surgery he developed pseudophakic retinal detachment which was successfully treated with pars plana vitrectomy and silicon oil tamponade. The silicon oil was removed one year after surgery. A year later he complained of increasing blurred vision in the left eye. Clinical examination revealed vesicular alterations located superficially on the intraocular lens (IOL, which could not be removed by perflourocarbon-perflourohexloctane lavage. As the patient complained about increasing visual impairment, the IOL was removed. The IOL was investigated by electronmicroscopy and biochemical analysis. During electron microscopy and following biochemical analysis the observed alterations were identified as calcium-phosphate particles located on the superficial aspect of the IOL. The occurrence of calcium-phosphate deposits on a posterior chamber IOL after silicon oil tamponade is a rare complication and has not been described so far. As these deposits interfere with visual acuity, removal of the lens has to be considered.

  18. Melatonin plus porcine bone on discrete calcium deposit implant surface stimulates osteointegration in dental implants.

    Science.gov (United States)

    Calvo-Guirado, José Luis; Gómez-Moreno, Gerardo; Barone, Antonio; Cutando, Antonio; Alcaraz-Baños, Miguel; Chiva, Fernando; López-Marí, Laura; Guardia, Javier

    2009-09-01

    The aim of this study was to evaluate the effect of the topical application of melatonin mixed with collagenized porcine bone to accelerate the osteointegration on the rough discrete calcium deposit (DCD) surface implants in Beagle dogs 3 months after their insertion. In preparation for subsequent insertion of dental implants, lower premolars and molars were extracted from 12 Beagle dogs. Each mandible received three parallel wall implants with discrete calcium deposit (DCD) surface of 4 mm in diameter and 10 mm in length. The implants were randomly assigned to the distal sites on each side of the mandible in three groups: group I implants alone, group II implants with melatonin and group III implants with melatonin and porcine bone. Prior to implanting, 5 mg lyophylized powdered melatonin was applied to one bone hole at each side of the mandible. None was applied at the control sites. Ten histological sections per implant were obtained for histomorphometric studies. After a 4-wk treatment period, melatonin significantly increased the perimeter of bone that was in direct contact with the treated implants (P implants. Topical application of melatonin on DCD surface may act as a biomimetic agent in the placement of endo-osseous dental implants and enhance the osteointegration. Melatonin combined with porcine bone on DCD implants reveals more bone to implant contact at 12 wk (84.5 +/- 1.5%) compared with melatonin treated (75.1 +/- 1.4%) and nonmelatonin treated surface implants (64 +/- 1.4%).

  19. Characterization of calcium phosphate deposited on valve metal by anodic oxidation with polarity inversion.

    Science.gov (United States)

    Okawa, Seigo; Homma, Kikuo; Kanatani, Mitsugu; Watanabe, Kouichi

    2009-07-01

    Electrochemical deposition of calcium phosphate (CAP) on valve metals such as Ta, Nb, and Zr, was performed by anodic oxidation with alternate polarity inversion at an applied 20 VDC. A saturated hydroxyapatite(HAP)-phosphoric acid solution (pH 3) was used as the electrolyte. FTIR, XRD, and XPS were employed to investigate the detailed characteristics of the deposition. HAP was precipitated on Ta; HAP including brushite and monetite on Nb; and HAP and monetite on Zr. The Ca/P atomic ratios were 1.3-1.5 by XPS, and HPO(4)(2- )bands were detected on Ta by FTIR. Therefore, the HAP precipitated on Ta was a Ca-deficient HAP. In addition, the XPS spectra of the specimens showed that phosphate ions were incorporated into the anodic oxide film. Deposits with nano-grain size were observed by AFM. The results confirmed that CAP with nano-grain size was deposited on valve metals by the anodic oxidation with polarity inversion.

  20. Performance of separation processes for precipitated calcium carbonate produced with an innovative method from steelmaking slag and carbon dioxide

    Directory of Open Access Journals (Sweden)

    Sebastian eTeir

    2016-02-01

    Full Text Available In this work, experiments were performed to determine the filterability of calcium carbonate produced with an alternative calcium carbonate production concept. The concept uses steelmaking slag as raw material and has potential to fix CO2 emissions and utilize steelmaking slag, simultaneously. As calcium carbonate is precipitated in a solution containing ammonium chloride, calcium chloride and ammonia, the product needs to be washed and hence filtered. In this work different separation processes, including washing, filtering and drying, were tested on two calcium carbonate slurries produced from steel converter slag and CO2 by a laboratory-scale pilot facility, with the aim of obtaining a solid product with a low chloride content using a minimum amount of washing water. The order of maximum filtration rates achievable of the calcium carbonate slurries was determined by experimental work. The tests included pressure filtration and vacuum filtration and the test series contained altogether 21 different filtration cycles with varying combinations of filtering, washing, and drying steps. The filtered cakes were analyzed by their residual moisture content, chloride content and conductivity, and the filtrates by their residual solids content, chloride content and conductivity. Pressure filtration gave a high capacity (400-460 kg/m2h and a low cake residual moisture content (12-14 wt-%. Vacuum filtration gave slightly higher filtration rates (500-610 kg/m2h at the lowest residual chloride contents of the cakes, but the cake residual moisture also stayed higher (25-26 wt-%. As the vacuum filtration tests used a filter cloth with higher permeability than that of the pressure filtration tests, a slightly higher filtration rate was expected. However, both filtration technologies seem suitable for filtering and washing calcium carbonate prepared with the studied method as a residual chloride content as low as 10 ppm of the filtered solids can be achieved

  1. Plasma deposited diamond-like carbon films for large neutralarrays

    Energy Technology Data Exchange (ETDEWEB)

    Brown, I.G.; Blakely, E.A.; Bjornstad, K.A.; Galvin, J.E.; Monteiro, O.R.; Sangyuenyongpipat, S.

    2004-07-15

    To understand how large systems of neurons communicate, we need to develop methods for growing patterned networks of large numbers of neurons. We have found that diamond-like carbon thin films formed by energetic deposition from a filtered vacuum arc carbon plasma can serve as ''neuron friendly'' substrates for the growth of large neural arrays. Lithographic masks can be used to form patterns of diamond-like carbon, and regions of selective neuronal attachment can form patterned neural arrays. In the work described here, we used glass microscope slides as substrates on which diamond-like carbon was deposited. PC-12 rat neurons were then cultured on the treated substrates and cell growth monitored. Neuron growth showed excellent contrast, with prolific growth on the treated surfaces and very low growth on the untreated surfaces. Here we describe the vacuum arc plasma deposition technique employed, and summarize results demonstrating that the approach can be used to form large patterns of neurons.

  2. Measured black carbon deposition on the Sierra Nevada snow pack and implication for snow pack retreat

    Directory of Open Access Journals (Sweden)

    O. L. Hadley

    2010-04-01

    Full Text Available Modeling studies show that the darkening of snow and ice by black carbon (BC deposition is a major factor for the rapid disappearance of arctic sea ice, mountain glaciers and snow packs. This study provides one of the first direct measurements for the efficient removal of black carbon from the atmosphere by snow and its subsequent deposition on the snow packs of California. The early melting of the snow packs in the Sierras is one of the contributing factors to the severe water problems in California. BC concentrations in falling snow were measured at two mountain locations and in rain at a coastal site. All three stations reveal large BC concentrations in precipitation, ranging from 1.7 ng/g to 12.9 ng/g. The BC concentrations in the air after the snow fall were negligible suggesting an extremely efficient removal of BC by snow. The data suggest that below cloud scavenging, rather than ice nuclei, was the dominant source of BC in the snow. A five-year comparison of BC, dust, and total fine aerosol mass concentrations at multiple sites reveals that the measurements made at the sampling sites were representative of large scale deposition in the Sierra Nevada. The relative concentration of iron and calcium in the mountain aerosol indicates that one-quarter to one-third of the BC may have been transported from Asia.

  3. Measured black carbon deposition on the Sierra Nevada snow pack and implication for snow pack retreat

    Directory of Open Access Journals (Sweden)

    O. L. Hadley

    2010-08-01

    Full Text Available Modeling studies show that the darkening of snow and ice by black carbon deposition is a major factor for the rapid disappearance of arctic sea ice, mountain glaciers and snow packs. This study provides one of the first direct measurements for the efficient removal of black carbon from the atmosphere by snow and its subsequent deposition to the snow packs of California. The early melting of the snow packs in the Sierras is one of the contributing factors to the severe water problems in California. BC concentrations in falling snow were measured at two mountain locations and in rain at a coastal site. All three stations reveal large BC concentrations in precipitation, ranging from 1.7 ng/g to 12.9 ng/g. The BC concentrations in the air after the snow fall were negligible suggesting an extremely efficient removal of BC by snow. The data suggest that below cloud scavenging, rather than ice nuclei, was the dominant source of BC in the snow. A five-year comparison of BC, dust, and total fine aerosol mass concentrations at multiple sites reveals that the measurements made at the sampling sites were representative of large scale deposition in the Sierra Nevada. The relative concentration of iron and calcium in the mountain aerosol indicates that one-quarter to one-third of the BC may have been transported from Asia.

  4. Measured Black Carbon Deposition on the Sierra Nevada Snow Pack and Implication for Snow Pack Retreat

    Energy Technology Data Exchange (ETDEWEB)

    Hadley, O.L.; Corrigan, C.E.; Kirchstetter, T.W.; Cliff, S.S.; Ramanathan, V.

    2010-01-12

    Modeling studies show that the darkening of snow and ice by black carbon deposition is a major factor for the rapid disappearance of arctic sea ice, mountain glaciers and snow packs. This study provides one of the first direct measurements for the efficient removal of black carbon from the atmosphere by snow and its subsequent deposition to the snow packs of California. The early melting of the snow packs in the Sierras is one of the contributing factors to the severe water problems in California. BC concentrations in falling snow were measured at two mountain locations and in rain at a coastal site. All three stations reveal large BC concentrations in precipitation, ranging from 1.7 ng/g to 12.9 ng/g. The BC concentrations in the air after the snow fall were negligible suggesting an extremely efficient removal of BC by snow. The data suggest that below cloud scavenging, rather than ice nuclei, was the dominant source of BC in the snow. A five-year comparison of BC, dust, and total fine aerosol mass concentrations at multiple sites reveals that the measurements made at the sampling sites were representative of large scale deposition in the Sierra Nevada. The relative concentration of iron and calcium in the mountain aerosol indicates that one-quarter to one-third of the BC may have been transported from Asia.

  5. Preferential soft-tissue preservation in the Hot Creek carbonate spring deposit, British Columbia, Canada

    Science.gov (United States)

    Rainey, Dustin K.; Jones, Brian

    2010-05-01

    The relict Holocene Hot Creek carbonate spring deposit in southeast British Columbia is characterized by excellent preservation of soft-tissue organisms (e.g. cyanobacteria), but poor preservation of organisms with hard-tissue (e.g. wood, diatoms). The deposit is formed mainly of calcified cyanobacteria, with fewer mineralized macrophytes (plants), bryophytes (mosses), wood, and diatoms. Cyanobacteria grew as solitary filaments ( Lyngbya) and as radiating hemispherical colonies ( Rivularia). Both were preserved by encrustation and encapsulation while alive, and as casts after filament death and decay. Sheath impregnation was rare to absent. Filament encrustation, whereby calcite crystals nucleated on, and grew away from the sheath exterior, produced moulds that replicated external filament morphology, but hastened filament decay. Filament encapsulation, whereby calcite nucleated in the vicinity of, and grew towards the encapsulated filament, promoted sheath preservation even after trichome decay. Subsequent calcite precipitation inside the hollow sheath generated sheath casts. The inability of mineralizing spring water to penetrate durable cell walls meant that bryophytes, macrophytes, and most wood was preserved by encrustation. Some wood resisted complete decay for several thousand years, and its lignified cell walls allowed rare permineralizations. Diatoms were not preserved in the relict deposit because the frustules were dissolved by the basic spring water. Amorphous calcium carbonate produced by photosynthetic CO 2 removal may have acted as nucleation sites for physicochemically precipitated calcite. Thus, metabolic activities of floral organisms probably initiated biotic mineralization, but continuous inorganic calcite precipitation on and in flora ensured that soft tissues were preserved.

  6. The influence of polyaspartate additive on the growth and morphology of calcium carbonate crystals

    Science.gov (United States)

    Gower, Laurie Anne

    The addition of low levels of polyaspartate to a supersaturated calcium carbonate (CaCOsb3) solution leads to unusual morphologies in the inorganic phase. Spherulitic vaterite aggregates with helical protrusions, and distorted calcite crystals that contain spiral pits, have been produced. The helical particles are coated with an inorganic membrane that appears to be responsible for the helical twist. The polymer also causes deposition of thin CaCOsb3 tablets and films on the glass substrate. Two distinct types of films are deposited; the first is a mosaic of calcite crystals, and the second is spherulitic vaterite. In situ observations of the crystallization reaction have determined that the thin-film morphology is a result of the phase separation of a hydrated CaCOsb3/polymer liquid-precursor, whereby accumulation of isotropic droplets creates a coating on the substrate, and subsequent dehydration and crystallization yields birefringent CaCOsb3 films. During the amorphous to crystalline transition, incremental growth steps lead to "transition bars" and sectored calcite tablets. This in vitro system was originally modeled after certain aspects of CaCOsb3 biomineralization, in which the soluble proteins extracted from biominerals tend to have high levels of aspartic acid residues. Based on the similarities between features exhibited by the products of this system and those in biominerals, an argument has been presented to suggest that this polymer-induced liquid-precursor (PILP) process is involved in the morphogenesis of CaCOsb3 biominerals. These features include the following: thin CaCOsb3 tablets that grow laterally; tablets that express unstable crystallographic faces; non-faceted single crystals with curved surfaces; spatially-delineated single crystals; sectored calcite tablets; hollow-shell spheres; calcium carbonate cements; and magnesium-bearing calcites. This work has demonstrated that a means of morphological control can be accomplished through non

  7. Electroless deposition of Cu on multiwalled carbon nanotubes

    Institute of Scientific and Technical Information of China (English)

    YUAN Dingsheng; LIU Yingliang

    2006-01-01

    Copper has been deposited on the surface of multiwalled carbon nanotubes (MWNTs) and inside MWNTs by electroless deposition. The as-prepared Cu-MWNT composite materials have been characterized by X-ray diffractometer(XRD), transmission electron microscopy (TEM), and electrochemical measurement. XRD analyses showed that Cu was a face-centered cubic (fcc) structure. The average size of Cu was calculated by Scherrer's formula from XRD data, and it was11 nm. TEM revealed that Cu grains on the surface of MWNTs were uniform with the sizes of about 30-60 nm. The electrochemical measurement indicated that Cu-MWNT composite materials possessed fine electron conductivity.

  8. Inhibition of Receptor Activator of NF-κB Ligand by Denosumab Attenuates Vascular Calcium Deposition in Mice

    Science.gov (United States)

    Helas, Susann; Goettsch, Claudia; Schoppet, Michael; Zeitz, Ute; Hempel, Ute; Morawietz, Henning; Kostenuik, Paul J.; Erben, Reinhold G.; Hofbauer, Lorenz C.

    2009-01-01

    Osteoporosis and vascular calcification frequently coincide. A potential mediator of bone metabolism and vascular homeostasis is the triad cytokine system, which consists of receptor activator of nuclear factor-κB (RANK) ligand (RANKL), its receptor RANK, and the decoy receptor osteoprotegerin. Unopposed RANKL activity in osteoprotegerin-deficient mice resulted in osteoporosis and vascular calcification. We therefore analyzed the effects of RANKL inhibition by denosumab, a human monoclonal antibody against RANKL, on vascular calcium deposition following glucocorticoid exposure. Prednisolone pellets were implanted into human RANKL knock-in (huRANKL-KI) mice, which unlike wild-type mice are responsive to denosumab. No histomorphological abnormalities or differences in aortic wall thickness were detected between wild-type and huRANKL-KI mice, regardless of treatment with prednisolone, denosumab, or both. However, concurrent treatment with denosumab reduced aortic calcium deposition of prednisolone-treated huRANKL-KI mice by up to 50%, based on calcium measurement. Of note, aortic calcium deposition in huRANKL-KI mice was correlated negatively with bone mineral density at the lumbar spine (P = 0.04) and positively with urinary excretion of deoxypyridinoline, a marker of bone resorption (P = 0.01). In summary, RANKL inhibition by denosumab reduced vascular calcium deposition in glucocorticoid-induced osteoporosis in mice, which is further evidence for the link between the bone and vascular systems. Therefore, the prevention of bone loss by denosumab might also be associated with reduced vascular calcification in certain conditions. PMID:19590040

  9. Inhibition of receptor activator of NF-kappaB ligand by denosumab attenuates vascular calcium deposition in mice.

    Science.gov (United States)

    Helas, Susann; Goettsch, Claudia; Schoppet, Michael; Zeitz, Ute; Hempel, Ute; Morawietz, Henning; Kostenuik, Paul J; Erben, Reinhold G; Hofbauer, Lorenz C

    2009-08-01

    Osteoporosis and vascular calcification frequently coincide. A potential mediator of bone metabolism and vascular homeostasis is the triad cytokine system, which consists of receptor activator of nuclear factor-kappaB (RANK) ligand (RANKL), its receptor RANK, and the decoy receptor osteoprotegerin. Unopposed RANKL activity in osteoprotegerin-deficient mice resulted in osteoporosis and vascular calcification. We therefore analyzed the effects of RANKL inhibition by denosumab, a human monoclonal antibody against RANKL, on vascular calcium deposition following glucocorticoid exposure. Prednisolone pellets were implanted into human RANKL knock-in (huRANKL-KI) mice, which unlike wild-type mice are responsive to denosumab. No histomorphological abnormalities or differences in aortic wall thickness were detected between wild-type and huRANKL-KI mice, regardless of treatment with prednisolone, denosumab, or both. However, concurrent treatment with denosumab reduced aortic calcium deposition of prednisolone-treated huRANKL-KI mice by up to 50%, based on calcium measurement. Of note, aortic calcium deposition in huRANKL-KI mice was correlated negatively with bone mineral density at the lumbar spine (P = 0.04) and positively with urinary excretion of deoxypyridinoline, a marker of bone resorption (P = 0.01). In summary, RANKL inhibition by denosumab reduced vascular calcium deposition in glucocorticoid-induced osteoporosis in mice, which is further evidence for the link between the bone and vascular systems. Therefore, the prevention of bone loss by denosumab might also be associated with reduced vascular calcification in certain conditions.

  10. Decoding depositional sequences in carbonate systems: Concepts vs experience

    Science.gov (United States)

    Pomar, Luis; Haq, Bilal U.

    2016-11-01

    Efficacy of sequence stratigraphic concepts in siliciclastic systems has been proven by successful applications in both academia and the industry over the past four decades. However, experience has demonstrated repeatedly that the relatively simple advective transportational approach of these models is less than successful when applied to the more complex carbonate systems and can lead to erroneous interpretations. Instead, an approach that includes the use of the changes in the biotic components of carbonate deposits to infer the sea-level trajectory and thereby placing it in the proper sequence framework is deemed to be more meaningful. This is exemplified with several well-studied examples that illustrate the variety of ways in which the biotic components can build carbonate platforms, and how these have changed through the ages prompted by biological evolution. This extended review discusses carbonate production, source to sink transportation influenced by sea-level changes, surface waves, as well as the less understood and under-appreciated internal waves, and the resulting variety of platforms that can be built by the interaction of these factors, as well as the changing patterns of biotic components with time. Their effect on the carbonate reservoir is considerable, understanding of which is the ultimate objective of carbonate research for applications in the industry. Key elements in the carbonate environments that differ from the siliciclastic systems are: 1) intrabasinal conditions (nutrients, salinity, temperature, water energy, transparency) are important controls on carbonate production and therefore also control in-situ accommodation and how it may be filled; 2) depositional accommodation can be both physical (controlled by hydrodynamics) and ecological (in the building-up above the base level mode); 3) because carbonates are products of biological activity, their production modes have been changing with time as their biotic components have evolved; 4

  11. Ubiquitylation functions in the calcium carbonate biomineralization in the extracellular matrix.

    Directory of Open Access Journals (Sweden)

    Dong Fang

    Full Text Available Mollusks shell formation is mediated by matrix proteins and many of these proteins have been identified and characterized. However, the mechanisms of protein control remain unknown. Here, we report the ubiquitylation of matrix proteins in the prismatic layer of the pearl oyster, Pinctada fucata. The presence of ubiquitylated proteins in the prismatic layer of the shell was detected with a combination of western blot and immunogold assays. The coupled ubiquitins were separated and identified by Edman degradation and liquid chromatography/mass spectrometry (LC/MS. Antibody injection in vivo resulted in large amounts of calcium carbonate randomly accumulating on the surface of the nacreous layer. These ubiquitylated proteins could bind to specific faces of calcite and aragonite, which are the two main mineral components of the shell. In the in vitro calcium carbonate crystallization assay, they could reduce the rate of calcium carbonate precipitation and induce the calcite formation. Furthermore, when the attached ubiquitins were removed, the functions of the EDTA-soluble matrix of the prismatic layer were changed. Their potency to inhibit precipitation of calcium carbonate was decreased and their influence on the morphology of calcium carbonate crystals was changed. Taken together, ubiquitylation is involved in shell formation. Although the ubiquitylation is supposed to be involved in every aspect of biophysical processes, our work connected the biomineralization-related proteins and the ubiquitylation mechanism in the extracellular matrix for the first time. This would promote our understanding of the shell biomineralization and the ubiquitylation processes.

  12. Effects of functional groups and soluble matrices in fish otolith on calcium carbonate mineralization

    Energy Technology Data Exchange (ETDEWEB)

    Ren Dongni; Li Zhuo; Gao Yonghua; Feng Qingling, E-mail: biomater@mail.tsinghua.edu.c [State Key Laboratory of New Ceramics and Fine Processing, Department of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China)

    2010-10-01

    Calcium carbonate mineralization is significantly influenced by organic matrices in vivo. The effect mainly relies on functional groups in proteins. In order to study the influence of functional groups on calcium carbonate mineralization, -OH, -NH{sub 2} and -COOH groups were grafted onto single crystal silicon chips, and such modified chips were used as substrates in in vitro mineralization experiments. An x-ray photoelectron spectroscopy (XPS) test was conducted to examine the grafting efficiency, and the three groups were successfully grafted. Calcium carbonate mineralization on a modified silicon substrate was examined by a scanning electron microscope (SEM) and x-ray diffraction (XRD), and the results showed that the effects of -OH, -NH{sub 2} and -COOH groups were quite different. Furthermore, a water-soluble protein matrix (WSM) and an acid-soluble protein matrix (ASM) extracted from fish otolith were adsorbed onto the -COOH-modified silicon substrate, and the effects of the protein matrices on calcium carbonate mineralization were studied. The results showed that both WSM and ASM of lapillus could mediate aragonite crystallization, but the size and morphology of the formed crystals were different. The WSM and ASM of asteriscus adsorbed on the silicon substrate had little effect on calcium carbonate mineralization; almost all the crystals were calcite, while both asteriscus WSM and ASM in solution could mediate vaterite crystals, and the morphologies of vaterite crystal aggregates were different.

  13. Adhesion property of epoxidized natural rubber (ENR-based adhesives containing calcium carbonate

    Directory of Open Access Journals (Sweden)

    2008-06-01

    Full Text Available The adhesion property (i.e. viscosity, loop tack and peel strength of epoxidized natural rubber (ENR 25 and ENR 50 grade-based pressure-sensitive adhesive was studied in the presence of calcium carbonate. The range of calcium carbonate loaded was from 10 to 50 parts per hundred parts of rubber (phr. Coumarone-indene resin was used as the tackifier and its concentration was fixed at 80 phr. Toluene was chosen as the solvent throughout the investigation. The substrates (PET film/paper were coated with the adhesive using a SHEEN hand coater at a coating thickness of 60 µm. Viscosity of the adhesive was measured by a HAAKE Rotary Viscometer whereas loop tack and peel strength were determined by a Llyod Adhesion Tester operating at 30 cm/min. Results show that viscosity of ENR-based adhesives increases gradually with increase in calcium carbonate loading due to the concentration effect of the filler. However, for loop tack and peel strength, it passes through a maximum at 30 phr calcium carbonate, an observation which is attributed to the optimum wettability of adhesive on the substrate at this adhesive composition. ENR 25-based adhesive consistently exhibits higher adhesion property than ENR 50 for all calcium carbonate loadings studied.

  14. Recovery of calcium carbonate from steelmaking slag and utilization for acid mine drainage pre-treatment.

    Science.gov (United States)

    Mulopo, J; Mashego, M; Zvimba, J N

    2012-01-01

    The conversion of steelmaking slag (a waste product of the steelmaking process) to calcium carbonate (CaCO(3)) was tested using hydrochloric acid, ammonium hydroxide and carbon dioxide via a pH-swing process. Batch reactors were used to assess the technical feasibility of calcium carbonate recovery and its use for pre-treatment of acid mine drainage (AMD) from coal mines. The effects of key process parameters, such as the amount of acid (HCl/calcium molar ratio), the pH and the CO(2) flow rate were considered. It was observed that calcium extraction from steelmaking slag significantly increased with an increase in the amount of hydrochloric acid. The CO(2) flow rate also had a positive effect on the carbonation reaction rate but did not affect the morphology of the calcium carbonate produced for values less than 2 L/min. The CaCO(3) recovered from the bench scale batch reactor demonstrated effective neutralization ability during AMD pre-treatment compared with the commercial laboratory grade CaCO(3).

  15. Calcium-decorated carbon nanostructures for the selective capture of carbon dioxide.

    Science.gov (United States)

    Koo, Jahyun; Bae, Hyeonhu; Kang, Lei; Huang, Bing; Lee, Hoonkyung

    2016-10-26

    The development of advanced materials for CO2 capture is of great importance for mitigating climate change. In this paper, we outline our discovery that calcium-decorated carbon nanostructures, i.e., zigzag graphene nanoribbons (ZGNRs), carbyne, and graphyne, have great potential for selective CO2 capture, as demonstrated via first-principles calculations. Our findings show that Ca-decorated ZGNRs can bind up to three CO2 molecules at each Ca atom site with an adsorption energy of ∼-0.8 eV per CO2, making them suitable for reversible CO2 capture. They adsorb CO2 molecules preferentially, compared with other gas molecules such as H2, N2, and CH4. Moreover, based on equilibrium thermodynamical simulations, we confirm that Ca-decorated ZGNRs can capture CO2 selectively from a gas mixture with a capacity of ∼4.5 mmol g(-1) under ambient conditions. Similar results have been found in other carbon nanomaterials, indicating the generality of carbon based nanostructures for selective CO2 capture under ambient conditions.

  16. Elucidating the Effect of Biomolecule Structure on Calcium Carbonate Crystal Formation

    Science.gov (United States)

    Kulbok, K. E.; Duckworth, O.

    2011-12-01

    Anthropogenic emissions of carbon dioxide have lead to a steady increase in atmospheric concentration. This greenhouse gas has been identified as a key driver of climate change and also has lead to increased acidification of marine and terrestrial waters. Calcium carbonate precipitation at the Earth's surface is an integral linkage in the global carbon cycle, especially in regards to regulating atmospheric carbon dioxide. As concern for the effect of increasing atmospheric CO2 levels grows, the need to understand calcium carbonate systems escalates concurrently. Calcium carbonate phases are the most abundant group of biominerals; therefore, elucidating the mechanism of biomineralization is critical to understanding CaCO3 precipitation and may aid in the development of novel carbon sequestration strategies. The ubiquity of microorganisms leads to an extensive number of biomolecules present in the Earth's systems, and thus an extensive range of possible effects on CaCO3 formation. Carboxylic acids are very common biomolecules and have a relatively simple structure, thus making them an ideal family of model compounds. This study examines the kinetics, thermodynamics, phase, and morphology of calcium carbonate crystals precipitated in the presence of carboxylate-containing biomolecules, including citric acid, succinic acid, and aspartic acid. The experiments utilize a unique (NH4)2CO3 gas-diffusion reactor, which allows in-situ measurements of chemical conditions during the precipitation and growth of crystals. Continuous monitoring of the in-situ conditions of pCO2, pH, [Ca2+], and optical absorbance provides data on the supersaturation at which nucleation occurs and the kinetics of mineral growth. The use of scanning electron microscopy and X-ray diffraction provides information on the morphology and mineralogy of precipitates. The combination of these data sets will provide an in-depth view of the ideal concentration of calcium ions required for solution saturation

  17. Molten carbonate fuel cell reduction of nickel deposits

    Energy Technology Data Exchange (ETDEWEB)

    Smith, James L. (Lemont, IL); Zwick, Stanley A. (Darien, IL)

    1987-01-01

    A molten carbonate fuel cell with anode and cathode electrodes and an eleolyte formed with two tile sections, one of the tile sections being adjacent the anode and limiting leakage of fuel gas into the electrolyte with the second tile section being adjacent the cathode and having pores sized to permit the presence of oxygen gas in the electrolyte thereby limiting the formation of metal deposits caused by the reduction of metal compositions migrating into the electrolyte from the cathode.

  18. Nitrogen Deposition Effects on Soil Carbon Dynamics in Temperate Forests

    DEFF Research Database (Denmark)

    Ginzburg Ozeri, Shimon

    Soils contain the largest fraction of terrestrial carbon (C). Understanding the factors regulating the decomposition and storage of soil organic matter (SOM) is essential for predictions of the C sink strength of the terrestrial environment in the light of global change. Elevated long-term nitrogen...... (N) deposition into forest ecosystems has been increasing globally and was hypothesized to raise soil organic C (SOC) stocks by increasing forest productivity and by reducing SOM decomposition. Yet, these effects of N deposition on forest SOC stocks are uncertain and largely based on observations...... edges were used to study the effects of varying N deposition load on SOC stocks and fluxes as well as on the temperature sensitivity of SOM respiration. In a third study, the effects of 20 years of continuous experimental N addition (35 kg N ha-1 year-1) on soil C budget were investigated. Our general...

  19. Production of carbon molecular sieves from palm shell through carbon deposition from methane

    Directory of Open Access Journals (Sweden)

    Mohammadi Maedeh

    2011-01-01

    Full Text Available The possibility of production of carbon molecular sieve (CMS from palm shell as a waste lignocellulosic biomass was investigated. CMS samples were prepared through heat treatment processes including carbonization, physiochemical activation and chemical vapor deposition (CVD from methane. Methane was pyrolyzed to deposit fine carbon on the pore mouth of palm shell-based activated carbon to yield CMS. All the deposition experiments were performed at 800 ºC, while the methane flow rate (100, 200, 300 mL min-1 CH4 diluted in 500 mL min-1 N2 and deposition time (30 to 60 min were the investigated parameters. The textural characteristics of the CMSs were assessed by N2 adsorption. The largest BET surface area (752 m2 g-1, micropore surface area (902.2 m2 g-1 and micropore volume (0.3466 cm3 g-1 was obtained at the CH4 flow rate of 200 mL min-1 and deposition time of 30 min. However, prolonging the deposition time to 45 min yielded in a micropouros CMS with a narrow pore size distribution.

  20. Preparation and mechanism of calcium phosphate coatings on chemical modified carbon fibers by biomineralization

    Institute of Scientific and Technical Information of China (English)

    HUANG Su-ping; ZHOU Ke-chao; LI Zhi-you

    2008-01-01

    In order to prepare HA coatings on the carbon fibers, chemical modification and biomineralization processes were applied. The phase components, morphologies, and possible growth mechanism of calcium phosphate were studied by infrared spectroscopy(IR), X-ray diffractometry(XRD) and scanning electron microscopy(SEM). The results show that calcium phosphate coating on carbon fibers can be obtained by biomineralization. But the phase components and morphologies of calcium phosphate coatings are different due to different modification methods. Plate-like CaHPO4-2H2O (DCPD) crystals grow from one site of the active centre by HNO3 treatment. While on the para-aminobenzoic acid treated fibers, the coating is composed of nano-structural HA crystal homogeneously. This is because the -COOH functional groups of para-aminobenzoic acid graft on fibers, with negative charge and arranged structure, accelerating the HA crystal nucleation and crystallization on the carbon fibers.

  1. Synthesis of novel amorphous calcium carbonate by sono atomization for reactive mixing.

    Science.gov (United States)

    Kojima, Yoshiyuki; Kanai, Makoto; Nishimiya, Nobuyuki

    2012-03-01

    Droplets of several micrometers in size can be formed in aqueous solution by atomization under ultrasonic irradiation at 2 MHz. This phenomenon, known as atomization, is capable of forming fine droplets for use as a reaction field. This synthetic method is called SARM (sono atomization for reactive mixing). This paper reports on the synthesis of a novel amorphous calcium carbonate formed by SARM. The amorphous calcium carbonate, obtained at a solution concentration of 0.8 mol/dm(3), had a specific surface area of 65 m(2)/g and a composition of CaCO(3)•0.5H(2)O as determined using thermogravimetric/differential thermal analysis (TG-DTA). Because the ACC had a lower hydrate composition than conventional amorphous calcium carbonate (ACC), the ACC synthesized in this paper was very stable at room temperature.

  2. Plasma-enhanced Deposition of Nano-Structured Carbon Films

    Institute of Scientific and Technical Information of China (English)

    Yang Qiaoqin (杨巧勤); Xiao Chijin (肖持进); A. Hirose

    2005-01-01

    By pre-treating substrate with different methods and patterning the catalyst, selective and patterned growth of diamond and graphitic nano-structured carbon films have been realized through DC Plasma-Enhanced Hot Filament Chemical Vapor Deposition (PE-HFCVD).Through two-step processing in an HFCVD reactor, novel nano-structured composite diamond films containing a nanocrystalline diamond layer on the top of a nanocone diamond layer have been synthesized. Well-aligned carbon nanotubes, diamond and graphitic carbon nanocones with controllable alignment orientations have been synthesized by using PE-HFCVD. The orientation of the nanostructures can be controlled by adjusting the working pressure. In a Microwave Plasma Enhanced Chemical Vapor Deposition (MW-PECVD) reactor, high-quality diamond films have been synthesized at low temperatures (310 ℃~550 ℃) without adding oxygen or halogen gas in a newly developed processing technique. In this process, carbon source originates from graphite etching, instead of hydrocarbon. The lowest growth temperature for the growth of nanocrystalline diamond films with a reasonable growth rate without addition of oxygen or halogen is 260 ℃.

  3. Factors Controlling Black Carbon Deposition in Snow in the Arctic

    Science.gov (United States)

    Qi, L.; Li, Q.; He, C.; Li, Y.

    2015-12-01

    This study evaluates the sensitivity of black carbon (BC) concentration in snow in the Arctic to BC emissions, dry deposition and wet scavenging efficiency using a 3D global chemical transport model GEOS-Chem driven by meteorological field GEOS-5. With all improvements, simulated median BC concentration in snow agrees with observation (19.2 ng g-1) within 10%, down from -40% in the default GEOS-Chem. When the previously missed gas flaring emissions (mainly located in Russia) are included, the total BC emission in the Arctic increases by 70%. The simulated BC in snow increases by 1-7 ng g-1, with the largest improvement in Russia. The discrepancy of median BC in snow in the whole Arctic reduces from -40% to -20%. In addition, recent measurements of BC dry deposition velocity suggest that the constant deposition velocity of 0.03 cm s-1 over snow and ice used in the GEOS-Chem is too low. So we apply resistance-in-series method to calculate the dry deposition velocity over snow and ice and the resulted dry deposition velocity ranges from 0.03 to 0.24 cm s-1. However, the simulated total BC deposition flux in the Arctic and BC in snow does not change, because the increased dry deposition flux has been compensated by decreased wet deposition flux. However, the fraction of dry deposition to total deposition increases from 16% to 25%. This may affect the mixing of BC and snow particles and further affect the radative forcing of BC deposited in snow. Finally, we reduced the scavenging efficiency of BC in mixed-phase clouds to account for the effect of Wegener-Bergeron-Findeisen (WBF) process based on recent observations. The simulated BC concentration in snow increases by 10-100%, with the largest increase in Greenland (100%), Tromsø (50%), Alaska (40%), and Canadian Arctic (30%). Annual BC loading in the Arctic increases from 0.25 to 0.43 mg m-2 and the lifetime of BC increases from 9.2 to 16.3 days. This indicates that BC simulation in the Arctic is really sensitive to

  4. Skeletal development in Acropora cervicornis: I. Patterns of calcium carbonate accretion in the axial corallite

    Science.gov (United States)

    Gladfeiter, E. H.

    1982-06-01

    Scanning electron microscopy and serial petrographic thin sections were used to investigate skeletal elongation and mineralization in the perforate coral, Acropora cervicornis. The axial corallite extends by the formation of randomly oriented fusiform crystals which are deposited on its distal edge. Aragonitic needle-like crystals grow in random directions from the surface of these fusiform crystals. Only those needle-like crystals growing toward the calicoblastic epithelium (i.e. crystals whose growth axis is perpendicular to the plane of the calicoblastic cell membrane) continue to elongate. Groups of these growing crystals join to form well-defined fasciculi which make up the primary skeletal elements comprising the septotheca. The resulting skeleton is highly porous with all surfaces covered by the continuous calicoblastic epithelium. This cell layer is separated by thin mesoglea from the flagellated gastrodermis which lines the highly ramified coelenteron. Porosity and permeability of the skeleton decrease with distance from the tip. Density correspondingly increases due to the addition of aragonite to the fasciculi whose boundaries become less distinct as channels fill with calcium carbonate.

  5. Synthesis of carbon molecular sieves by activation and coke deposition

    Energy Technology Data Exchange (ETDEWEB)

    Vyas, S.N.; Patwardhan, S.R.; Vijayalakshmi, S.; Gandadhar, B. (Indian Institute of Technology, Bombay (India). Dept. of Chemical Engineering)

    1993-04-01

    Carbon molecular sieves were synthesized from indigenous bituminous coal and coconut shell. After preliminary treatment, these materials were subjected to steam or carbon dioxide activation in the range 500-900[degree]C. In other experiments the raw materials were partly air-oxidized at [approximately] 200[degree]C, mixed with binder and extruded to cylindrical pellets, which were subjected to coke deposition by cracking of methane in the range 750-780[degree]C for 5-14 min. All the products were characterized by analysis of kinetic and equilibrium adsorption data. The molecular sieve performance was judged by the O[sub 2]/N[sub 2] uptake ratio. The best carbon molecular sieves, obtained by methane cracking at 780[degree]C at a flow of 100 ml min[sup -1] had an uptake ratio of 2.667. 11 refs., 7 figs., 5 tabs.

  6. Plasma Enhanced Chemical Vapour Deposition of Horizontally Aligned Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    Matthew T. Cole

    2013-05-01

    Full Text Available A plasma-enhanced chemical vapour deposition reactor has been developed to synthesis horizontally aligned carbon nanotubes. The width of the aligning sheath was modelled based on a collisionless, quasi-neutral, Child’s law ion sheath where these estimates were empirically validated by direct Langmuir probe measurements, thereby confirming the proposed reactors ability to extend the existing sheath fields by up to 7 mm. A 7 mbar growth atmosphere combined with a 25 W plasma permitted the concurrent growth and alignment of carbon nanotubes with electric fields of the order of 0.04 V μm−1 with linear packing densities of up to ~5 × 104 cm−1. These results open up the potential for multi-directional in situ alignment of carbon nanotubes providing one viable route to the fabrication of many novel optoelectronic devices.

  7. The influence of electron discharge and magnetic field on calcium carbonate (CaCO3) precipitation

    Science.gov (United States)

    Putro, Triswantoro; Endarko

    2016-04-01

    The influences of electron discharge and magnetic field on calcium carbonate (CaCO3) precipitation in water have been successfully investigated. The study used three pairs of magnetic field 0.1 T whilst the electron discharge was generated from television flyback transformer type BW00607 and stainless steel SUS 304 as an electrode. The water sample with an initial condition of 230 mg/L placed in the reactor with flow rate 375 mL/minutes, result showed that the electron discharge can be reduced contain of calcium carbonate the water sample around 17.39% within 2 hours. Meanwhile for the same long period of treatment and flow rate, around 56.69% from initial condition of 520 mg/L of calcium carbonate in the water sample can be achieved by three pairs of magnetic field 0.1 T. When the combination of three pairs of magnetic field 0.1 T and the electron discharge used for treatment, the result showed that the combination of electron discharge and magnetic field methods can be used to precipitate calcium carbonate in the water sample 300 mg/L around 76.66% for 2 hours of treatment. The study then investigated the influence of the polar position of the magnetic field on calcium carbonate precipitation. Two positions of magnetic field were tested namely the system with alternated polar magnetics and the system without inversion of the polar magnetics. The influence of the polar position showed that the percentage reduction in levels of calcium carbonate in the water sample (360 mg/L) is significant different. Result showed that the system without inversion of the polar magnetics is generally lower than the system with alternated polar magnetics, with reduction level at 30.55 and 57.69%, respectively.

  8. Calcium in diet

    Science.gov (United States)

    ... D is needed to help your body use calcium. Milk is fortified with vitamin D for this reason. ... of calcium dietary supplements include calcium citrate and calcium carbonate. Calcium citrate is the more expensive form of ...

  9. Characterization of Carbon Deposits Formed During Plasma Pyrolysis of Xinjiang Candle Coal

    Science.gov (United States)

    Zhu, Guilin; Meng, Yuedong; Shu, Xingsheng; Fang, Shidong

    2009-08-01

    Carbon deposits were formed on the reactor wall during plasma pyrolysis of the Xinjiang candle coal in our V-style plasma pyrolysis pilot-plant. The carbon deposits were studied using a scanning electronic microscope (SEM) and the X-ray diffraction (XRD) method. It was found that carbon deposits located at different parts in the reactor exhibited different microscopic patterns. The formation mechanism of the carbon deposits was deduced. The downward increase in the graphitization degree of the carbon deposits was found and interpreted.

  10. Characterization of carbon deposits formed during plasma pyrolysis of Xinjiang candle coal

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, G.L.; Meng, Y.D.; Shu, X.S.; Fang, S.D. [Chinese Academy of Sciences, Hefei (China). Inst. of Plasma Physics

    2009-08-15

    Carbon deposits were formed on the reactor wall during plasma pyrolysis of the Xinjiang candle coal in our V-style plasma pyrolysis pilot-plant. The carbon deposits were studied using a scanning electronic microscope (SEM) and the X-ray diffraction (XRD) method. It was found that carbon deposits located at different parts in the reactor exhibited different microscopic patterns. The formation mechanism of the carbon deposits was deduced. The down ward increase in the graphitization degree of the carbon deposits was found and interpreted

  11. Mechanisms controlling soil carbon sequestration under atmospheric nitrogen deposition

    Energy Technology Data Exchange (ETDEWEB)

    R.L. Sinsabaugh; D.R. Zak; D.L. Moorhead

    2008-02-19

    Increased atmospheric nitrogen (N) deposition can alter the processing and storage of organic carbon in soils. In 2000, we began studying the effects of simulated atmospheric N deposition on soil carbon dynamics in three types of northern temperate forest that occur across a wide geographic range in the Upper Great Lakes region. These ecosystems range from 100% oak in the overstory (black oak-white oak ecosystem; BOWO) to 0% overstory oak (sugar maple-basswood; SMBW) and include the sugar maple-red oak ecosystem (SMRO) that has intermediate oak abundance. The leaf litter biochemistry of these ecosystems range from highly lignified litter (BOWO) to litter of low lignin content (SMBW). We selected three replicate stands of each ecosystem type and established three plots in each stand. Each plot was randomly assigned one of three levels of N deposition (0, 30 & 80 kg N ha-1 y-1) imposed by adding NaNO3 in six equal increments applied over the growing season. Through experiments ranging from the molecular to the ecosystem scales, we produced a conceptual framework that describes the biogeochemistry of soil carbon storage in N-saturated ecosystems as the product of interactions between the composition of plant litter, the composition of the soil microbial community and the expression of extracellular enzyme activities. A key finding is that atmospheric N deposition can increase or decrease the soil C storage by modifying the expression of extracellular enzymes by soil microbial communities. The critical interactions within this conceptual framework have been incorporated into a new class of simulations called guild decomposition models.

  12. MINERALIZATION STUDY OF RENAL RATS FOLLOWING OVARYOHYSTERECTOMY AND ADMINISTRATION HIGH DOSE CALCIUM CARBONATE

    OpenAIRE

    Wiwik Misaco Yuniarti; Ira Sari Yudaniayanti; Nusdianto Triakoso

    2008-01-01

    The aim of this study was to determine the effect of high dose calcium carbonate in rat (Rattus norvegicus) following ovaryohysterectomy. A total of twenty female rats at 13 week-old were used in this study. Following ovaryohitectomy, the animals were randomized in four treatment groups. Group P0 were :fed with standard food only P1, P2 and P2 groups treated with standard food but supplemented calcium carbonate respectively at the dose of 75 mg per animal per day, 225 mg per animal per day , ...

  13. Porous tablets of crystalline calcium carbonate via sintering of amorphous nanoparticles

    OpenAIRE

    Gebauer, Denis; Liu, Xing-Min; Aziz, Baroz; Hedin, Niklas; Zhao, Zhe

    2013-01-01

    Porous tablets of crystalline calcium carbonate were formed upon sintering of a precursor powder of amorphous calcium carbonate (ACC) under compressive stress (20 MPa) at relatively low temperatures (120–400 °C), induced by pulsed direct currents. Infrared spectroscopy ascertained the amorphous nature of the precursor powders. At temperatures of 120–350 °C and rates of temperature increase of 20–100 °C min−1, the nanoparticles of ACC transformed into crystallites of mainly aragonite, which is...

  14. {sup 41}Ca as a tracer for calcium uptake and deposition in heart tissue during ischemia and reperfusion

    Energy Technology Data Exchange (ETDEWEB)

    Southon, J.R. [Lawrence Livermore National Lab., CA (United States); Bishop, M.S.; Kost, G.J. [California Univ., Davis, CA (United States). Dept. of Medical Pathology and Biomedical Engineering

    1993-09-17

    We have developed techniques and are commencing experiments using enriched {sup 41}Ca as a tracer in isolated rabbit heart preparations. The aims of the study are to measure calcium uptake and deposition in response to cardiac ischemia and reperfusion, and to investigate events and mechanism leading to irreversible myocyte injury.

  15. Chemical analysis and molecular models for calcium-oxygen-carbon interactions in black carbon found in fertile Amazonian anthrosoils.

    Science.gov (United States)

    Archanjo, Braulio S; Araujo, Joyce R; Silva, Alexander M; Capaz, Rodrigo B; Falcão, Newton P S; Jorio, Ado; Achete, Carlos A

    2014-07-01

    Carbon particles containing mineral matter promote soil fertility, helping it to overcome the rather unfavorable climate conditions of the humid tropics. Intriguing examples are the Amazonian Dark Earths, anthropogenic soils also known as "Terra Preta de Índio'' (TPI), in which chemical recalcitrance and stable carbon with millenary mean residence times have been observed. Recently, the presence of calcium and oxygen within TPI-carbon nanoparticles at the nano- and mesoscale ranges has been demonstrated. In this work, we combine density functional theory calculations, scanning transmission electron microscopy, energy dispersive X-ray spectroscopy, Fourier transformed infrared spectroscopy, and high resolution X-ray photoelectron spectroscopy of TPI-carbons to elucidate the chemical arrangements of calcium-oxygen-carbon groups at the molecular level in TPI. The molecular models are based on graphene oxide nanostructures in which calcium cations are strongly adsorbed at the oxide sites. The application of material science techniques to the field of soil science facilitates a new level of understanding, providing insights into the structure and functionality of recalcitrant carbon in soil and its implications for food production and climate change.

  16. Treatment of oil–water emulsions by adsorption onto activated carbon, bentonite and deposited carbon

    OpenAIRE

    Khaled Okiel; Mona El-Sayed; Mohamed Y. El-Kady

    2011-01-01

    Emulsified oil in waste water constitutes is a severe problem in the different treatment stages before disposed off in a manner that does not violate environmental criteria. One commonly used technique for remediation of petroleum contaminated water is adsorption. The main objective of this study is to examine the removal of oil from oil–water emulsions by adsorption on bentonite, powdered activated carbon (PAC) and deposited carbon (DC). The results gave evidence of the ability of the adsorb...

  17. Raman spectra of amorphous carbon films deposited by SWP

    Science.gov (United States)

    Xu, Junqi; Liu, Weiguo; Hang, Lingxia; Su, Junhong; Fan, Huiqing

    2010-10-01

    Amorphous carbon film is one of the most important anti-reflection protective films coated on infrared optical components. In this paper, hydrogen-free amorphous carbon films were deposited by new type surface-wave-sustained plasma (SWP) source with a graphite target at various experiment parameters. The laser Raman spectroscopy at wavelength of 514 nm was used to investigate the structure and bonding of these carbon films. The results showed consanguineous correlations between the intensity ratio ID/IG and the experiment parameters such as microwave power, target voltage and gas pressure applied to the SWP source. Raman spectra proved the structure of these carbon films prepared by SWP technique is typical diamond-like carbon (DLC). The analysis on G peak position and intensity ratio ID/IG indicated that Raman shifts moves to low wavenumber and ID/IG decreases with the increasing of microwave power from 150 W to 330 W. These results means the formation of sp3 bond prefers higher microwave power. DLC films prepared at target voltage of -200 V have higher sp3 content than that of -350 V, moreover, an increase of gas pressure during experiments yields higher sp3 content at the microwave power below 270 W, whereas the change of sp3 content is slight with the various conditions when microwave power exceeds 270 W.

  18. Calcium phosphate/porous silicon biocomposites prepared by cyclic deposition methods: spin coating vs electrochemical activation.

    Science.gov (United States)

    Hernandez-Montelongo, J; Gallach, D; Naveas, N; Torres-Costa, V; Climent-Font, A; García-Ruiz, J P; Manso-Silvan, M

    2014-01-01

    Porous silicon (PSi) provides an excellent platform for bioengineering applications due to its biocompatibility, biodegradability, and bioresorbability. However, to promote its application as bone engineering scaffold, deposition of calcium phosphate (CaP) ceramics in its hydroxyapatite (HAP) phase is in progress. In that sense, this work focuses on the synthesis of CaP/PSi composites by means of two different techniques for CaP deposition on PSi: Cyclic Spin Coating (CSC) and Cyclic Electrochemical Activation (CEA). Both techniques CSC and CEA consisted on alternate Ca and P deposition steps on PSi. Each technique produced specific morphologies and CaP phases using the same independent Ca and P stem-solutions at neutral pH and at room temperature. The brushite (BRU) phase was favored with the CSC technique and the hydroxyapatite (HAP) phase was better synthesized using the CEA technique. Analyses by elastic backscattering spectroscopy (EBS) on CaP/PSi structures synthesized by CEA supported that, by controlling the CEA parameters, an HAP coating with the required Ca/P atomic ratio of 1.67 can be promoted. Biocompatibility was evaluated by bone-derived progenitor cells, which grew onto CaP/PSi prepared by CSC technique with a long-shaped actin cytoskeleton. The density of adhered cells was higher on CaP/PSi prepared by CEA, where cells presented a normal morphological appearance and active mitosis. These results can be used for the design and optimization of CaP/PSi composites with enhanced biocompatibility for bone-tissue engineering.

  19. Calcium phosphate/porous silicon biocomposites prepared by cyclic deposition methods: Spin coating vs electrochemical activation

    Energy Technology Data Exchange (ETDEWEB)

    Hernandez-Montelongo, J., E-mail: jacobo.hernandez@uam.es [Departamento de Física Aplicada, Universidad Autónoma de Madrid, 28049 Madrid (Spain); Gallach, D.; Naveas, N.; Torres-Costa, V. [Departamento de Física Aplicada, Universidad Autónoma de Madrid, 28049 Madrid (Spain); Climent-Font, A. [Departamento de Física Aplicada, Universidad Autónoma de Madrid, 28049 Madrid (Spain); Centro de Microanálisis de Materiales (CMAM), Universidad Autónoma de Madrid, Madrid 28049 (Spain); García-Ruiz, J.P. [Departamento de Biología Molecular, Universidad Autónoma de Madrid, Cantoblanco, Madrid 28049 (Spain); Manso-Silvan, M. [Departamento de Física Aplicada, Universidad Autónoma de Madrid, 28049 Madrid (Spain)

    2014-01-01

    Porous silicon (PSi) provides an excellent platform for bioengineering applications due to its biocompatibility, biodegradability, and bioresorbability. However, to promote its application as bone engineering scaffold, deposition of calcium phosphate (CaP) ceramics in its hydroxyapatite (HAP) phase is in progress. In that sense, this work focuses on the synthesis of CaP/PSi composites by means of two different techniques for CaP deposition on PSi: Cyclic Spin Coating (CSC) and Cyclic Electrochemical Activation (CEA). Both techniques CSC and CEA consisted on alternate Ca and P deposition steps on PSi. Each technique produced specific morphologies and CaP phases using the same independent Ca and P stem-solutions at neutral pH and at room temperature. The brushite (BRU) phase was favored with the CSC technique and the hydroxyapatite (HAP) phase was better synthesized using the CEA technique. Analyses by elastic backscattering spectroscopy (EBS) on CaP/PSi structures synthesized by CEA supported that, by controlling the CEA parameters, an HAP coating with the required Ca/P atomic ratio of 1.67 can be promoted. Biocompatibility was evaluated by bone-derived progenitor cells, which grew onto CaP/PSi prepared by CSC technique with a long-shaped actin cytoskeleton. The density of adhered cells was higher on CaP/PSi prepared by CEA, where cells presented a normal morphological appearance and active mitosis. These results can be used for the design and optimization of CaP/PSi composites with enhanced biocompatibility for bone-tissue engineering. - Highlights: • Proposed cyclic methods produce specific morphologies and CaP phases in biocomposites. • The brushite phase is favored in the biocomposite produced by Cyclic Spin Coating. • The hydroxyapatite phase is favored in the biocomposite produced by Cyclic Electrochemical Activation. • The Ca/P atomic ratio of hydroxyapatite was validated by elastic backscattering spectroscopy. • Cells grown showed morphological and

  20. Fractionation behavior of chromium isotopes during coprecipitation with calcium carbonate

    DEFF Research Database (Denmark)

    Rodler, Alexandra; Sánchez-Pastor, Nuria; Fernández-Díaz, Lurdes;

    2015-01-01

    Interest in chromium (Cr) isotope incorporation into carbonates arises from the observation that Cr isotopic composition of carbonates could be used as a paleoclimate proxy to elucidate past fluctuations of oxygen contents in atmosphere and hydrosphere. The use of Cr isotopes to track paleoenviro......Interest in chromium (Cr) isotope incorporation into carbonates arises from the observation that Cr isotopic composition of carbonates could be used as a paleoclimate proxy to elucidate past fluctuations of oxygen contents in atmosphere and hydrosphere. The use of Cr isotopes to track...

  1. Effects of Sigma Anti-bonding Molecule Calcium Carbonate on bone turnover and calcium balance in ovariectomized rats.

    Science.gov (United States)

    Choi, So-Young; Park, Dongsun; Yang, Goeun; Lee, Sun Hee; Bae, Dae Kwon; Hwang, Seock-Yeon; Lee, Paul K; Kim, Yun-Bae; Kim, Ill-Hwa; Kang, Hyun-Gu

    2011-12-01

    This study was conducted to evaluate the effect of Sigma Anti-bonding Molecule Calcium Carbonate (SAC) as therapy for ovariectomy-induced osteoporosis in rats. Three weeks after surgery, fifteen ovariectomized Sprague-Dawley rats were divided randomly into 3 groups: sham-operated group (sham), ovariectomized group (OVX) and SAC-treatment group (OVX+SAC). The OVX+SAC group was given drinking water containing 0.0012% SAC for 12 weeks. Bone breaking force and mineralization as well as blood parameters related to the bone metabolism were analyzed. In OVX animals, blood concentration of 17β-estradiol decreased significantly, while osteocalcin and type I collagen C-terminal telopeptides (CTx) increased. Breaking force, bone mineral density (BMD), calcium and phosphorus in femurs, as well as uterine and vaginal weights, decreased significantly following OVX. However, SAC treatment (0.0012% in drinking water) not only remarkably restored the decreased 17β-estradiol and increased osteocalcin and CTx concentrations, but also recovered decreased femoral breaking force, BMD, calcium and phosphorus, although it did not reversed reproductive organ weights. It is suggested that SAC effectively improve bone density by preventing bone turnover mediated osteocalcin, CTx and minerals, and that it could be a potential candidate for therapy or prevention of postmenopausal osteoporosis.

  2. MINERALIZATION STUDY OF RENAL RATS FOLLOWING OVARYOHYSTERECTOMY AND ADMINISTRATION HIGH DOSE CALCIUM CARBONATE

    Directory of Open Access Journals (Sweden)

    Wiwik Misaco Yuniarti

    2008-06-01

    Full Text Available The aim of this study was to determine the effect of high dose calcium carbonate in rat (Rattus norvegicus following ovaryohysterectomy. A total of twenty female rats at 13 week-old were used in this study. Following ovaryohitectomy, the animals were randomized in four treatment groups. Group P0 were :fed with standard food only P1, P2 and P2 groups treated with standard food but supplemented calcium carbonate respectively at the dose of 75 mg per animal per day, 225 mg per animal per day , and 450 mg per animal per day. The calcium carbonate supplement were given daily in the morning for 42 days. The experimental animals were sacrificed at 21 week-old. Calcium and phosphor level in sinister kidneys were determined by spectrofotometric method. The data obtained from this study were analysed using one way analysis of variance. No significant difference was observed in calcium level among four treatment groups, with the lowest level were found in P3 group. However, the phosphor level of P1 was significantly lower than those of P2 and P3 groups. The highest phosphor level was observed in P3 group, indicating a phosphorous retension and the signs of renal failure.

  3. Synthesis of porous poly(acrylamide hydrogels using calcium carbonate and its application for slow release of potassium nitrate

    Directory of Open Access Journals (Sweden)

    2009-05-01

    Full Text Available Porous poly(acrylamide was synthesized using calcium carbonate microparticles and subsequent acid treatment to remove the calcium carbonate. Methylenebisacrylamide and ammonium persulfate/sodium metabisulfite were used as crosslinking agent and redox initiator, respectively. The porous structure of resulted hydrogels was confirmed using SEM micrographs. The effect of methylenebisacrylamide concentration and calcium carbonate amount on the swelling of the hydrogels was investigated. The results showed that the effect of methylenebisacrylamide and calcium carbonate variables on the swelling is reverse. The hydrogels were subsequently utilized for the loading of potassium nitrate. Potassium nitrate as active agent was loaded into hydrogels and subsequently the release of this active agent was investigated. In these series of investigation, the effect of content of loading, methylenebisacrylamide and calcium carbonate amount on the release of potassium nitrate from hydrogels was investigated.

  4. Properties of electrophoretically deposited single wall carbon nanotube films

    Energy Technology Data Exchange (ETDEWEB)

    Lim, Junyoung; Jalali, Maryam; Campbell, Stephen A., E-mail: campb001@umn.edu

    2015-08-31

    This paper describes techniques for rapidly producing a carbon nanotube thin film by electrophoretic deposition at room temperature and determines the film mass density and electrical/mechanical properties of such films. The mechanism of electrophoretic deposition of thin layers is explained with experimental data. Also, film thickness is measured as a function of time, electrical field and suspension concentration. We use Rutherford backscattering spectroscopy to determine the film mass density. Films created in this manner have a resistivity of 2.14 × 10{sup −3} Ω·cm, a mass density that varies with thickness from 0.12 to 0.54 g/cm{sup 3}, and a Young's modulus between 4.72 and 5.67 GPa. The latter was found to be independent of thickness from 77 to 134 nm. We also report on fabricating free-standing films by removing the metal seed layer under the CNT film, and selectively etching a sacrificial layer. This method could be extended to flexible photovoltaic devices or high frequency RF MEMS devices. - Highlights: • We explain the electrophoretic deposition process and mechanism of thin SWCNT film deposition. • Characterization of the SWCNT film properties including density, resistivity, transmittance, and Young's modulus. • The film density and resistivity are found to be a function of the film thickness. • Techniques developed to create free standing layers of SW-CNTs for flexible electronics and mechanical actuators.

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

    Science.gov (United States)

    Kramer, Henry

    1956-01-01

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

  6. The Deposition of Gold Nanoparticles Onto Activated Carbon

    Directory of Open Access Journals (Sweden)

    Jaworski W.

    2014-10-01

    Full Text Available This work reports the results of spectrophotometric, dynamic light scattering (DLS and microscopic (SEM studies of the gold nanoparticles (AuNPs deposition on activated carbon (AC surface modified with primary (ethanolamine and secondary (diethylenetriamine and triethylenetetramine amines. It was found that this method is efficient for deposition of AuNPs from aqueous solution. However, nanoparticles change their morphology depending on the kind of amine used in experiments. On the AC surface modified with ethanolamine, the uniform spherical AuNPs were formed. In case of diethylenetriamine and triethylenetetramine application, the agglomerates of AuNPs are present. The diameter of individual AuNPs did not exceed 15 nm and was bigger as compared with the diameter of particles present in precursor solution (ca. 10 nm.

  7. Constant-distance mode scanning potentiometry. 1. Visualization of calcium carbonate dissolution in aqueous solution.

    Science.gov (United States)

    Etienne, Mathieu; Schulte, Albert; Mann, Stefan; Jordan, Guntram; Dietzel, Irmgard D; Schuhmann, Wolfgang

    2004-07-01

    Constant-distance mode scanning potentiometry was established by integrating potentiometric microsensors as ion-selective scanning probes into a SECM setup that was equipped with a piezoelectric shear force-based tip-to-sample distance control. The combination of specially designed micrometer-sized potentiometric tips with an advanced system for tip positioning allowed simultaneous acquisition of both topographic and potentiometric information at solid/liquid interfaces with high spatial resolution. The performance of the approach was evaluated by applying Ca(2+)-selective constant-distance mode potentiometry to monitor the dissolution of calcium carbonate occurring either at the (104) surface of calcite crystals or in proximity to the more complex surface of cross sections of a calcium carbonate shell of Mya arenaria exposed to slightly acidic aqueous solutions. Micrometer-scale heterogeneities in the apparent calcium activity profiles have successfully been resolved for both samples.

  8. Sputtering deposition and characterization of ultrathin amorphous carbon films

    Science.gov (United States)

    Lu, Wei

    1999-11-01

    This dissertation focuses on experimental investigations of ultrathin, ultrasmooth amorphous carbon (a-C) films deposited on Si(100) substrates by radio frequency (RF) sputtering and characterization of the nanomechanical and nanotribological properties and thermal stability of the films. Ultrathin a-C films of thickness 5--100 nm and typical root-mean-square roughness of 0.15--1 nm were deposited on ultrasmooth Si(100) substrates using pure argon as the sputtering gas. A low-pressure RF argon discharge model was used to analyze the plasma parameters in the film growth environment. These plasma parameters correlate the deposition conditions with the film growth processes. Atomic force microscopy (AFM) and surface force microscopy (SFM) were used to characterize the nanomechanical and nanotribological properties of the a-C films. X-ray photoelectron spectroscopy (XPS) was used to investigate the compositions and microstructures of the films. Sputter-etching measurements of the a-C films by energetic argon ion bombardment were used to study the surface binding energy of carbon atoms in a-C films deposited under different conditions. The dependence of film properties on deposition conditions was studied, and relations between nanomechanical and nanotribological properties were discussed in terms of a modified deformation index. The deformation and nanotribology mechanisms of the a-C films were compared with those of other films, such as TiC and Cr films (both 100 nm thick), and bulk Si(100). Reactive RF sputtering of nitrogenated amorphous carbon (a-CNx) films was investigated by introducing nitrogen into the a-C films during film growth by using an argon-nitrogen gas mixture as the sputtering gas. The alloying effect of nitrogen on the film growth and properties, such as hardness and surface energy, was studied and interpreted in terms of the changes in the plasma environment induced due to differences in the composition of the sputtering gas mixture. The thermal

  9. Formation of carbon deposits from coal in an arc plasma

    Energy Technology Data Exchange (ETDEWEB)

    Wang, B.; Tian, Y.; Zhang, Y.; Zhu, S.; Lu, Y.; Zhang, Y.; Xie, K. [Taiyuan University of Technology, Taiyuan (China)

    2007-07-01

    The issue of deposited carbon (DC) on a reactor wall during the production of acetylene by the coal/arc plasma process is a potential obstacle for the industrialization process. The formation mechanism of DC is very difficult to reveal because the high complexity of coal and the volatile matter. Combining with quenching technique, the methane, liquid petroleum gas and benzene were employed as the model materials to roughly act as the light gas, chain and aromatic subcomponents of volatile matter, and then the reasonable formation mechanism of DC was subtly speculated accordingly.

  10. Kinetics and Mechanism of Decomposition of Nano-sized Calcium Carbonate under Non-isothermal Condition

    Institute of Scientific and Technical Information of China (English)

    刘润静; 陈建峰; 郭奋; 吉米; 沈志刚

    2003-01-01

    Experiments on thermal decomposition of nano-sized calcium carbonate were carried out in a thermo-gravimetric analyzer under non-isothermal condition of different heating rates (5 to 20K·min-1). The Coats and Redfern''s equation was used to determine the apparent activation energy and the pre-exponential factors. The mechanism of thermal decomposition was evaluated using the master plots, Coats and Redfern's equation and the kinetic compensation law. It was found that the thermal decomposition property of nano-sized calcium carbonate was different from that of bulk calcite. Nano-sized calcium carbonate began to decompose at 640℃, which was 180℃ lower than the reported value for calcite. The experimental results of kinetics were compatible with the mechanism of one-dimensional phase boundary movement. The apparent activation energy of nano-sized calcium carbonate was estimated to be 151 kJ·mo1-1 while the literature value for normal calcite was approximately 200 kJ ·mol-1. The order of magnitude of Dre-exvonential factors was estimated to be 109 s-1.

  11. Preparation and Characterization of Three-dimensional Chrysanthemun Flower-like Calcium Carbonate

    Institute of Scientific and Technical Information of China (English)

    CHEN Xianyong; TANG Qin; LIU Daijun; HU Weibing; DAN Youmeng

    2012-01-01

    Calcium carbonate with three-dimensional chrysanthemun flower-like structure was successfully prepared from calcium chloride and sodium carbonate ethanol/water mixed solution by a simple precipitation method,using trisodium citrate as crystal modifier.The experimental results show that the threedimensional structure of chrysanthemun flower-like calcium carbonate is built up with several symmetrical micrometer multi-layer petals arranged around the multi-layer pancake-liked center,and the micrometer center and petals are assemblied by a large number of nanometer spherical particles with size 10-20 nm.It is found that the amount of trisodium citrate,the ethanol volume content has an important influence on the formation of this morphology.A possible mechanism is proposed to explain the formation of three-dimensional chrysanthemun flower-like calcium carbonate according the results.Scanning electron microscopy (SEM),X-ray powder diffraction (XRD),flourier transform infrared spectroscopy (FT-IR),thermogravimety analysis (TG),transmission electron microscopy (TEM) equipped with energy-dispersive X-ray (EDX),and selected area electron diffraction (SAED) were used to characterize the crystals.

  12. Calcium carbonate crystallization controlled by functional groups: A mini-review

    Institute of Scientific and Technical Information of China (English)

    Hua DENG; Xing-Can SHEN; Xiu-Mei WANG; Chang DU

    2013-01-01

    Various functional groups have been suggested to play essential roles on biomineralization of calcium carbonate (CaCO3) in natural system. 2D and 3D models of regularly arranged functional groups have been established to investigate their effect on CaCO3 crystallization, This mini-review summarizes the recent progress and the future development is prospected.

  13. Soil tillage, water erosion, and calcium, magnesium and organic carbon losses

    Directory of Open Access Journals (Sweden)

    Bertol Ildegardis

    2005-01-01

    Full Text Available Soil tillage influences water erosion, and consequently, losses of calcium, magnesium and organic carbon in surface runoff. Nutrients and organic carbon are transported by surface runoff in particulate form, adsorbed to soil colloids or soluble in water, depending on the soil tillage system. This study was carried out on an Inceptisol, representative of the Santa Catarina highlands, southern Brazil, between November 1999 and October 2001, under natural rainfall. The soil tillage treatments (no replications were: no-tillage (NT, minimum soil tillage with chiseling + disking (MT, and conventional soil tillage with plowing + two diskings (CT. The crop cycles sequence was soybean (Glycine max, oats (Avena sativa, beans (Phaseolus vulgaris and vetch (Vicia sativa. Conventional soil tillage treatment with plowing + two disking in the absence of crops (BS was also studied. Calcium and magnesium concentrations were determined in both water and sediments of the surface runoff, while organic carbon was measured only in sediments. Calcium and magnesium concentrations were greater in sediments than in surface runoff, while total losses of these elements were greater in surface runoff than in sediments. The greatest calcium and magnesium concentrations in surface runoff were obtained under CT, while in sediments the greatest concentration occurred under MT. Organic carbon concentration in sediments did not differ under the different soil tillage systems, and the greatest total loss was under CT system.

  14. Calcium carbonate production of the mare incognitum, the upper windward reef slope, at enewetak atoll.

    Science.gov (United States)

    Smith, S V; Harrison, J T

    1977-08-05

    Corals and algal pavement produce calcium carbonate more slowly on the windward reef slope of Enewetak Atoll than on the reef flat despite the high standing crop of reef-building organisms on the slope. The capacity of reefs to remain at or near sea level is therefore not determined primarily by growth on the seaward slope.

  15. Amorphous and crystalline calcium carbonate distribution in the tergite cuticle of moulting Porcellio scaber (Isopoda, Crustacea).

    Science.gov (United States)

    Neues, Frank; Hild, Sabine; Epple, Matthias; Marti, Othmar; Ziegler, Andreas

    2011-07-01

    The main mineral components of the isopod cuticle consists of crystalline magnesium calcite and amorphous calcium carbonate. During moulting isopods moult first the posterior and then the anterior half of the body. In terrestrial species calcium carbonate is subject to resorption, storage and recycling in order to retain significant fractions of the mineral during the moulting cycle. We used synchrotron X-ray powder diffraction, elemental analysis and Raman spectroscopy to quantify the ACC/calcite ratio, the mineral phase distribution and the composition within the anterior and posterior tergite cuticle during eight different stages of the moulting cycle of Porcellio scaber. The results show that most of the amorphous calcium carbonate (ACC) is resorbed from the cuticle, whereas calcite remains in the old cuticle and is shed during moulting. During premoult resorption of ACC from the posterior cuticle is accompanied by an increase within the anterior tergites, and mineralization of the new posterior cuticle by resorption of mineral from the anterior cuticle. This suggests that one reason for using ACC in cuticle mineralization is to facilitate resorption and recycling of cuticular calcium carbonate. Furthermore we show that ACC precedes the formation of calcite in distal layers of the tergite cuticle.

  16. Citrate effects on amorphous calcium carbonate (ACC) structure, stability, and crystallization

    DEFF Research Database (Denmark)

    Tobler, Dominique Jeanette; Rodriguez Blanco, Juan Diego; Dideriksen, Knud;

    2015-01-01

    Understanding the role of citrate in the crystallization kinetics of amorphous calcium carbonate (ACC) is essential to explain the formation mechanisms, stabilities, surface properties, and morphologies of CaCO3 biominerals. It also contributes to deeper insight into fluid-mineral inte...

  17. Introduction of enzymatically degradable poly(trimethylene carbonate) microspheres into an injectable calcium phosphate cement

    NARCIS (Netherlands)

    Habraken, Wouter J. E. M.; Zhang, Zheng; Wolke, Joop G. C.; Grijpma, Dirk W.; Mikos, Antonios G.; Feijen, Jan; Jansen, John A.

    2008-01-01

    Poly(trimethylene carbonate) (PTMC) is an enzymatically degradable polyester with rubber-like properties. Introduction of this polymer into an injectable calcium phosphate bone cement can therefore be used to introduce macroporosity into the cement for tissue engineering purposes as well as to impro

  18. Introduction of enzymatically degradable poly(trimethylene carbonate) microspheres into an injectable calcium phosphate cement.

    NARCIS (Netherlands)

    Habraken, W.J.E.M.; Zhang, Z.; Wolke, J.G.C.; Grijpma, D.W.; Mikos, A.G.; Feijen, J.; Jansen, J.A.

    2008-01-01

    Poly(trimethylene carbonate) (PTMC) is an enzymatically degradable polyester with rubber-like properties. Introduction of this polymer into an injectable calcium phosphate bone cement can therefore be used to introduce macroporosity into the cement for tissue engineering purposes as well as to impro

  19. Scientific Opinion on the safety assessment of the active substances, sodium erythorbate, sodium carbonate, sodium bicarbonate, iron sulphate, activated carbon, cellulose, calcium hydroxide, calcium chloride and water, for use as active system in food contact materials

    OpenAIRE

    2014-01-01

    This scientific opinion of EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids deals with the safety assessment of the active substances sodium erythorbate, sodium carbonate, sodium bicarbonate, iron sulfate, activated carbon, cellulose, calcium hydroxide, calcium chloride and water, used in mixture which is packed into sachets for absorbing oxygen/carbon dioxide emitting from/into the headspace surrounding packed food. All substances of this formulation have been e...

  20. Calcium oxalate crystal deposition in kidneys of hypercalciuric mice with disrupted type IIa sodium-phosphate cotransporter

    OpenAIRE

    Khan, Saeed R.; Glenton, Patricia A.

    2008-01-01

    The most common theories about the pathogenesis of idiopathic kidney stones consider precipitation of calcium phosphate (CaP) within the kidneys critical for the development of the disease. We decided to test the hypothesis that a CaP substrate can promote the deposition of calcium oxalate (CaOx) in the kidneys. Experimental hyperoxaluria was induced by feeding glyoxylate to male mice with knockout (KO) of NaPi IIa (Npt2a), a sodium-phosphate cotransporter. Npt2a KO mice are hypercalciuric an...

  1. Electronic state of polyaniline deposited on carbon nanotube or ordered mesoporous carbon templates

    Energy Technology Data Exchange (ETDEWEB)

    Bulusheva, L.G.; Fedorovskaya, E.O.; Okotrub, A.V.; Maximovskiy, E.A. [Nikolaev Institute of Inorganic Chemistry, SB RAS, 3 Acad. Lavrentiev ave., 630090 Novosibirsk (Russian Federation); Vyalikh, D.V. [Institute of Solid State Physics, Dresden University of Technology, 01062 Dresden (Germany); Chen, Xiaohong; Song, Huaihe [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029 (China)

    2011-11-15

    Polyaniline (PANI) has been deposited on a carbon template by chemical oxidation of aniline chloride in acidic aqueous medium using sodium persulfate as oxidant. Two kinds of templates were used: array of aligned multiwall carbon nanotubes (CNTs) grown on silicon substrate and ordered mesoporous carbon (OMC) material. Electronic structure of composites was examined using near-edge X-ray absorption spectroscopy and X-ray photoelectron spectroscopy. Analysis of the spectra showed that PANI developed on the CNT surface is mainly protonated while it contains a marked amount of imine (=N-) nitrogen when deposited into the porous of OMC. Testing of electrochemical cell indicated enhancement of performance of composite electrodes as compared with unsupported PANI. XPS N 1s spectra of composites of PANI with OMC material (PANI/OMC) and aligned multiwall CNTs (PANI/CNT). (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  2. Responses of Carbon Dynamics to Nitrogen Deposition in Typical Freshwater Wetland of Sanjiang Plain

    Directory of Open Access Journals (Sweden)

    Yang Wang

    2014-01-01

    Full Text Available The effects of nitrogen deposition (N-deposition on the carbon dynamics in typical Calamagrostis angustifolia wetland of Sanjiang Plain were studied by a pot-culture experiment during two continuous plant growing seasons. Elevated atmospheric N-deposition caused significant increases in the aboveground net primary production and root biomass; moreover, a preferential partition of carbon to root was also observed. Different soil carbon fractions gained due to elevated N-deposition and their response intensities followed the sequence of labile carbon > dissolved organic carbon > microbial biomass carbon, and the interaction between N-deposition and flooded condition facilitated the release of different carbon fractions. Positive correlations were found between CO2 and CH4 fluxes and liable carbon contents with N-deposition, and flooded condition also tended to facilitate CH4 fluxes and to inhibit the CO2 fluxes with N-deposition. The increases in soil carbon fractions occurring in the nitrogen treatments were significantly correlated with increases in root, aboveground parts, total biomass, and their carbon uptake. Our results suggested that N-deposition could enhance the contents of active carbon fractions in soil system and carbon accumulation in plant of the freshwater wetlands.

  3. Calcium carbonate mineralization: involvement of extracellular polymeric materials isolated from calcifying bacteria.

    Science.gov (United States)

    Ercole, Claudia; Bozzelli, Paola; Altieri, Fabio; Cacchio, Paola; Del Gallo, Maddalena

    2012-08-01

    This study highlights the role of specific outer bacterial structures, such as the glycocalix, in calcium carbonate crystallization in vitro. We describe the formation of calcite crystals by extracellular polymeric materials, such as exopolysaccharides (EPS) and capsular polysaccharides (CPS) isolated from Bacillus firmus and Nocardia calcarea. Organic matrices were isolated from calcifying bacteria grown on synthetic medium--in the presence or absence of calcium ions--and their effect on calcite precipitation was assessed. Scanning electron microscopy observations and energy dispersive X-ray spectrometry analysis showed that CPS and EPS fractions were involved in calcium carbonate precipitation, not only serving as nucleation sites but also through a direct role in crystal formation. The utilization of different synthetic media, with and without addition of calcium ions, influenced the biofilm production and protein profile of extracellular polymeric materials. Proteins of CPS fractions with a molecular mass between 25 and 70 kDa were overexpressed when calcium ions were present in the medium. This higher level of protein synthesis could be related to the active process of bioprecipitation.

  4. Effects of Sevelamer Hydrochloride and Calcium Carbonate on Renal Osteodystrophy in Hemodialysis Patients

    Science.gov (United States)

    Ferreira, Aníbal; Frazão, João Miguel; Monier-Faugere, Marie-Claude; Gil, Célia; Galvao, José; Oliveira, Carlos; Baldaia, Jorge; Rodrigues, Ilidio; Santos, Carla; Ribeiro, Silvia; Hoenger, Regula Mueller; Duggal, Ajay; Malluche, Hartmut H.

    2008-01-01

    Disturbances in mineral metabolism play a central role in the development of renal bone disease. In a 54-wk, randomized, open-label study, 119 hemodialysis patients were enrolled to compare the effects of sevelamer hydrochloride and calcium carbonate on bone. Biopsy-proven adynamic bone disease was the most frequent bone abnormality at baseline (59%). Serum phosphorus, calcium, and intact parathyroid hormone were well controlled in both groups, although calcium was consistently lower and intact parathyroid hormone higher among patients who were randomly assigned to sevelamer. Compared with baseline values, there were no changes in mineralization lag time or measures of bone turnover (e.g., activation frequency) after 1 yr in either group. Osteoid thickness significantly increased in both groups, but there was no significant difference between them. Bone formation rate per bone surface, however, significantly increased from baseline only in the sevelamer group (P = 0.019). In addition, of those with abnormal microarchitecture at baseline (i.e., trabecular separation), seven of 10 in the sevelamer group normalized after 1 yr compared with zero of three in the calcium group. In summary, sevelamer resulted in no statistically significant changes in bone turnover or mineralization compared with calcium carbonate, but bone formation increased and trabecular architecture improved with sevelamer. Further studies are required to assess whether these changes affect clinical outcomes, such as rates of fracture. PMID:18199805

  5. Evaluation of polymer efficiency on the inhibition of calcium carbonate scale in synthetic brines; Avaliacao da acao de polimeros sobre a inibicao de incrustacoes de carbonato de calcio em salmouras sinteticas

    Energy Technology Data Exchange (ETDEWEB)

    Freitas, Juliana M.; Rodrigues, Jessica S.; Loureiro, Tatiana S.; Lucas, Elizabete F.; Spinelli, Luciana S. [Universidade Federal do Rio de Janeiro, Instituto de Macromoleculas, Laboratorio de Macromoleculas e Coloides na Industria de Petroleo, RJ (Brazil)], e-mail: julianamatos@ima.ufrj.br

    2011-07-01

    The inorganic scale results in serious problems for oil production. This scale results from the incompatibility between the chemical compositions of formation water and injection, and the changes of thermodynamic system. These deposits consist mainly of calcium carbonate and barium sulfate. In order to prevent the formation of these deposits, the petroleum industry has made use of chemicals that act as scale inhibitors. The aim of this study was to test the ability of two types of polymeric inhibitors prevent the formation of calcium carbonate from brines of different compositions with high concentrations of calcium. The inhibitors were tested at varying concentrations and at fixed conditions of temperature, pH, pressure and time. The estimated effectiveness of each inhibitor was measured by complexometric titration. The inhibitor carboxylic acid-based (poly (maleic acid)) was more efficient at relatively low concentrations, which is important both economically and environmentally. (author)

  6. Ti-doped hydrogenated diamond like carbon coating deposited by hybrid physical vapor deposition and plasma enhanced chemical vapor deposition

    Science.gov (United States)

    Lee, Na Rae; Sle Jun, Yee; Moon, Kyoung Il; Sunyong Lee, Caroline

    2017-03-01

    Diamond-like carbon films containing titanium and hydrogen (Ti-doped DLC:H) were synthesized using a hybrid technique based on physical vapor deposition (PVD) and plasma enhanced chemical vapor deposition (PECVD). The film was deposited under a mixture of argon (Ar) and acetylene gas (C2H2). The amount of Ti in the Ti-doped DLC:H film was controlled by varying the DC power of the Ti sputtering target ranging from 0 to 240 W. The composition, microstructure, mechanical and chemical properties of Ti-doped DLC:H films with varying Ti concentrations, were investigated using Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), nano indentation, a ball-on-disk tribometer, a four-point probe system and dynamic anodic testing. As a result, the optimum composition of Ti in Ti-doped DLC:H film using our hybrid method was found to be a Ti content of 18 at. %, having superior electrical conductivity and high corrosion resistance, suitable for bipolar plates. Its hardness value was measured to be 25.6 GPa with a low friction factor.

  7. Tamarind (Tamarindus indica) fruit shell carbon: A calcium-rich promising adsorbent for fluoride removal from groundwater.

    Science.gov (United States)

    Sivasankar, V; Rajkumar, S; Murugesh, S; Darchen, A

    2012-07-30

    Tamarindus indica fruit shells (TIFSs) are naturally calcium rich compounds. They were impregnated with ammonium carbonate and then carbonized, leading to ammonium carbonate activated ACA-TIFS carbon. The resulting materials and carbon arising from virgin fruit shells V-TIFS were characterized and assayed as adsorbent for the removal of fluoride anions from groundwater. The fluoride scavenging ability of TIFS carbons was due to naturally dispersed calcium compounds. X-ray diffraction (XRD) showed that TIFS carbon contained a mixture of calcium oxalate and calcium carbonate. Batch studies on the fluoride removal efficiency of TIFS carbons with respect to contact time, pH, initial fluoride concentration, and co-ion interference were conducted. Applicability of various kinetic models (viz., pseudo-first-order, pseudo-second-order, intra-particle diffusion and Elovich) and sorption isotherms were tested for batch techniques. The fluoride removal capacity of TIFS carbons was found to be 91% and 83% at a pH of 7.05 for V-TIFS and ACA-TIFS carbons, respectively. The practical applicability of TIFS carbons using groundwater samples was approved. The fluoride removal was greater in groundwater without hydrogen carbonate ions than those containing these ions. The characterizations of fluoride unloaded and loaded TIFS carbons were done by SEM and XRD studies.

  8. New Method of Depositing the Nanostructured Amorphous Carbon for Carbon Based Solar Cell Applications

    Directory of Open Access Journals (Sweden)

    A. N. Fadzilah

    2013-01-01

    Full Text Available Nanostructured amorphous carbon (a-C solar cells were successfully deposited via a self-designed aerosol-assisted chemical vapor deposition (AACVD. The fabricated solar cell with the configuration of Au/p-C/n-Si/Au achieved efficiency ( of % for device deposited at 500°C, % for 450°C, and % for 400°C. Photoresponse characteristic was highlighted under illumination (AM 1.5 illuminations: 100 mW/cm2, 25°C, where conductivity increased when the sample was being hit by light. Transmittance spectrum exhibits a large transmittance value (85% and absorption coefficient value of  cm−1 at the visible range from 390 to 790 nm. The nanostructured a-C thin film deposited at higher temperature possesses lower transmittance due to higher absorption as a result of the higher content of sp2-bonded carbon atoms. From Tauc’s plot, optical band gap ( was determined, and decreased as deposition temperature increased (1.2 eV, 1.0 eV, 0.7 eV. On the other hand, FESEM images exhibited a nanostructured sized a-C with the particle size less than 100 nm. To the best of our knowledge, the presence of nanostructured particle of a-C by a self-prepared AACVD has not frequently been reported.

  9. Methods of Boron-carbon Deposited Film Removal

    Science.gov (United States)

    Airapetov, A.; Terentiev, V.; Voituk, A.; Zakharov, A.

    Boron carbide was proposed as a material for in-situ renewable protecting coating for tungsten tiles of the ITER divertor. It is necessary to develop a method of gasification of boron-carbon film which deposits during B4C sputtering. In this paper the results of the first stage investigation of gasification methods of boron-carbon films are presented. Two gasification methods of films are investigated: interaction with the ozone-oxygen mixture and irradiation in plasma with the working gas composed of oxygen, ethanol, and, in some cases, helium. The gasification rate in the ozone-oxygen mixture at 250 °C for B/C films with different B/C ratio and carbon fiber composite (CFC), was measured. For B/C films the gasification rate decreased with increasing B/C ratio (from 45 nm/h at B/C=0.7 to 4 nm/h at B/C=2.1; for CFC - 15 μm/h). Films gasification rates were measured under ion irradiation from ethanol-oxygen-helium plasma at different temperatures, with different ion energies and different gas mixtures. The maximum obtained removal rate was near 230 nm/h in case of ethanol-oxygen plasma and at 150°C of the sample temperature.

  10. Microbially-Mediated Precipitation of Calcium Carbonate Nanoparticles.

    Science.gov (United States)

    Kang, Ser Ku; Roh, Yul

    2016-02-01

    The objective of this study was to investigate the biomineralization of carbonate minerals using microorganisms (Wu Do-1) enriched from rhodoliths. A 16S rRNA sequence analysis showed that Wu Do-1 mainly contained Proteus mirabilis. The pH decreased from 6.5 to 5.3 over the first 4 days of incubation due to microbial oxidation of organic acids, after which it increased to 7.8 over the remaining incubation period. XRD analysis showed that the precipitates were Mg-rich cal- cite (MgxCa(1-x)CO3), whereas no precipitates were formed without the addition of Wu Do-1 in D-1 medium. SEM-EDS analyses showed that the Mg-rich calcite had a rhombohedron shape and consisted of Ca, Si and Mg with an extracelluar polymeric substance (EPS). In addition, TEM-EDS analyses revealed they were hexagon in shape, 500-700 nm in size, and composed of Ca, Mg, C, and O. These results indicated that Wu Do-1 induced precipitation of Mg-rich calcite on the cell walls and EPS via the accumulation of Ca and/or Mg ions. Therefore, microbial precipitation of carbonate nanoparticles may play an important role in metal and carbon biogeochemistry, as well as in carbon sequestration in natural environments.

  11. Ocean acidification accelerates net calcium carbonate loss in a coral rubble community

    Science.gov (United States)

    Stubler, Amber D.; Peterson, Bradley J.

    2016-09-01

    Coral rubble communities are an important yet often overlooked component of a healthy reef ecosystem. The organisms inhabiting reef rubble are primarily bioeroders that contribute to the breakdown and dissolution of carbonate material. While the effects of ocean acidification on calcifying communities have been well studied, there are few studies investigating the response of bioeroding communities to future changes in pH and calcium carbonate saturation state. Using a flow-through pH-stat system, coral rubble pieces with a naturally occurring suite of organisms, along with bleached control rubble pieces, were subjected to three different levels of acidification over an 8-week period. Rates of net carbonate loss in bleached control rubble doubled in the acidification treatments (0.02 vs. 0.04% CaCO3 d-1 in ambient vs. moderate and high acidification), and living rubble communities experienced significantly increased rates of net carbonate loss from ambient to high acidification conditions (0.06 vs. 0.10% CaCO3 d-1, respectively). Although more experimentation is necessary to understand the long-term response and succession of coral rubble communities under projected conditions, these results suggest that rates of carbonate loss will increase in coral rubble as pH and calcium carbonate saturation states are reduced. This study demonstrates a need to thoroughly investigate the contribution of coral rubble to the overall carbonate budget, reef resilience, recovery, and function under future conditions.

  12. Ossifying tendinitis of the rotator cuff after arthroscopic excision of calcium deposits: report of two cases and literature review.

    Science.gov (United States)

    Merolla, Giovanni; Dave, Arpit C; Paladini, Paolo; Campi, Fabrizio; Porcellini, Giuseppe

    2015-03-01

    Ossifying tendinitis (OT) is a type of heterotopic ossification, characterized by deposition of hydroxyapatite crystals in a histologic pattern of mature lamellar bone. It is usually associated with surgical intervention or trauma and is more commonly seen in Achilles or distal biceps tendons, and also in the gluteus maximus tendon. To our knowledge, there is no description of OT as a complication of calcifying tendinitis of the rotator cuff. In this report, we describe two cases in which the patients developed an OT of the supraspinatus after arthroscopic removal of calcium deposits. The related literature is reviewed.

  13. A review: Different methods producing different particles size and distribution in synthesis of calcium carbonate nano particles

    Science.gov (United States)

    Sulimai, N. H.; Rusop, M.; Alrokayan, Salman A. H.; Khan, Haseeb A.

    2016-07-01

    Carbonates exist as 73 percent of world crust carbon. Abundance and bioavailability of Calcium Carbonates offer reliable resources, costs saving and environmental friendly potentials in its applications. Studies proven nano-sized Calcium Cabonate (nCC) employs a more significant characteristics compared to larger sizes. Properties of nCC is affected by the dispersion of the particles in which agglomeration occurs. It is important to gain more understanding of the conditions contributing or stunting the agglomeration to gain more control of the particles morphology and dynamic. A few recent studies with different methods to prepare calcium carbonate nanoparticles were listed in Table 1 .Particle size and dispersity of calcium carbonate are affected by different conditions of its preparation. Other factors such as mechanical aggression, concentration of solution, temperature of precipitation, pH of reaction are all contributing factors towards particle sizes and distribution.

  14. An unusual isotopic fractionation of boron in synthetic calcium carbonate precipitated from seawater and saline water

    Institute of Scientific and Technical Information of China (English)

    XIAO Yingkai; LI Shizhen; WEI Haizhen; SUN Aide; ZHOU Weijian; LIU Weiguo

    2006-01-01

    Inorganic calcium carbonate precipitation from natural seawater and saline water at various pH values was carried out experimentally. The results show the clear positive relationships between boron concentration and δ11B of inorganic calcium carbonate with the pH of natural seawater and saline water. However, the variations of boron isotopic fractionation between inorganic calcite and seawater/saline water with pH are inconsistent with the hypothesis that B(OH)4- is the dominant species incorporated into the biogenic calcite structure. The isotopic fractionation factors α Between synthetic calcium carbonate precipitate and parent solutions increase systematically as pH increases, from 0.9884 at pH 7.60 to 1.0072 at pH 8.60 for seawater and from 0.9826 at pH 7.60 to 1.0178 at pH 8.75 for saline water. An unusual boron isotopic fractionation factor of larger than 1 in synthetic calcium carbonate precipitated from seawater/saline water at higher pH is observed, which implies that a substantial amount of the isotopically heavier B(OH)3 species must be incorporated preferentially into synthetic inorganic carbonate. The results propose that the incorporation of B(OH)3 is attributed to the formation of Mg(OH)2 at higher pH of calcifying microenvironment during the synthetic calcium carbonate precipitation. The preliminary experiment of Mg(OH)2 precipitated from artificial seawater shows that heavier 11B is enriched in Mg(OH)2 precipitation, which suggests that isotopically heavier B(OH)3 species incorporated preferentially into Mg(OH)2 precipitation.This result cannot be applied to explain the boron isotopic fractionation of marine bio-carbonate because of the possibility that the unusual environment in this study appears in formation of marine bio-carbonate is infinitesimal. We, however, must pay more attention to this phenomenon observed in this study, which accidentally appears in especially natural environment.

  15. Geophysical monitoring and reactive transport modeling of ureolytically-driven calcium carbonate precipitation.

    Science.gov (United States)

    Wu, Yuxin; Ajo-Franklin, Jonathan B; Spycher, Nicolas; Hubbard, Susan S; Zhang, Guoxiang; Williams, Kenneth H; Taylor, Joanna; Fujita, Yoshiko; Smith, Robert

    2011-09-23

    Ureolytically-driven calcium carbonate precipitation is the basis for a promising in-situ remediation method for sequestration of divalent radionuclide and trace metal ions. It has also been proposed for use in geotechnical engineering for soil strengthening applications. Monitoring the occurrence, spatial distribution, and temporal evolution of calcium carbonate precipitation in the subsurface is critical for evaluating the performance of this technology and for developing the predictive models needed for engineering application. In this study, we conducted laboratory column experiments using natural sediment and groundwater to evaluate the utility of geophysical (complex resistivity and seismic) sensing methods, dynamic synchrotron x-ray computed tomography (micro-CT), and reactive transport modeling for tracking ureolytically-driven calcium carbonate precipitation processes under site relevant conditions. Reactive transport modeling with TOUGHREACT successfully simulated the changes of the major chemical components during urea hydrolysis. Even at the relatively low level of urea hydrolysis observed in the experiments, the simulations predicted an enhanced calcium carbonate precipitation rate that was 3-4 times greater than the baseline level. Reactive transport modeling results, geophysical monitoring data and micro-CT imaging correlated well with reaction processes validated by geochemical data. In particular, increases in ionic strength of the pore fluid during urea hydrolysis predicted by geochemical modeling were successfully captured by electrical conductivity measurements and confirmed by geochemical data. The low level of urea hydrolysis and calcium carbonate precipitation suggested by the model and geochemical data was corroborated by minor changes in seismic P-wave velocity measurements and micro-CT imaging; the latter provided direct evidence of sparsely distributed calcium carbonate precipitation. Ion exchange processes promoted through NH4

  16. Geophysical monitoring and reactive transport modeling of ureolytically-driven calcium carbonate precipitation

    Directory of Open Access Journals (Sweden)

    Taylor Joanna

    2011-09-01

    Full Text Available Abstract Ureolytically-driven calcium carbonate precipitation is the basis for a promising in-situ remediation method for sequestration of divalent radionuclide and trace metal ions. It has also been proposed for use in geotechnical engineering for soil strengthening applications. Monitoring the occurrence, spatial distribution, and temporal evolution of calcium carbonate precipitation in the subsurface is critical for evaluating the performance of this technology and for developing the predictive models needed for engineering application. In this study, we conducted laboratory column experiments using natural sediment and groundwater to evaluate the utility of geophysical (complex resistivity and seismic sensing methods, dynamic synchrotron x-ray computed tomography (micro-CT, and reactive transport modeling for tracking ureolytically-driven calcium carbonate precipitation processes under site relevant conditions. Reactive transport modeling with TOUGHREACT successfully simulated the changes of the major chemical components during urea hydrolysis. Even at the relatively low level of urea hydrolysis observed in the experiments, the simulations predicted an enhanced calcium carbonate precipitation rate that was 3-4 times greater than the baseline level. Reactive transport modeling results, geophysical monitoring data and micro-CT imaging correlated well with reaction processes validated by geochemical data. In particular, increases in ionic strength of the pore fluid during urea hydrolysis predicted by geochemical modeling were successfully captured by electrical conductivity measurements and confirmed by geochemical data. The low level of urea hydrolysis and calcium carbonate precipitation suggested by the model and geochemical data was corroborated by minor changes in seismic P-wave velocity measurements and micro-CT imaging; the latter provided direct evidence of sparsely distributed calcium carbonate precipitation. Ion exchange processes

  17. Geophysical monitoring and reactive transport modeling of ureolytically-driven calcium carbonate precipitation

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Y.; Ajo-Franklin, J.B.; Spycher, N.; Hubbard, S.S.; Zhang, G.; Williams, K.H.; Taylor, J.; Fujita, Y.; Smith, R.

    2011-07-15

    Ureolytically-driven calcium carbonate precipitation is the basis for a promising in-situ remediation method for sequestration of divalent radionuclide and trace metal ions. It has also been proposed for use in geotechnical engineering for soil strengthening applications. Monitoring the occurrence, spatial distribution, and temporal evolution of calcium carbonate precipitation in the subsurface is critical for evaluating the performance of this technology and for developing the predictive models needed for engineering application. In this study, we conducted laboratory column experiments using natural sediment and groundwater to evaluate the utility of geophysical (complex resistivity and seismic) sensing methods, dynamic synchrotron x-ray computed tomography (micro-CT), and reactive transport modeling for tracking ureolytically-driven calcium carbonate precipitation processes under site relevant conditions. Reactive transport modeling with TOUGHREACT successfully simulated the changes of the major chemical components during urea hydrolysis. Even at the relatively low level of urea hydrolysis observed in the experiments, the simulations predicted an enhanced calcium carbonate precipitation rate that was 3-4 times greater than the baseline level. Reactive transport modeling results, geophysical monitoring data and micro-CT imaging correlated well with reaction processes validated by geochemical data. In particular, increases in ionic strength of the pore fluid during urea hydrolysis predicted by geochemical modeling were successfully captured by electrical conductivity measurements and confirmed by geochemical data. The low level of urea hydrolysis and calcium carbonate precipitation suggested by the model and geochemical data was corroborated by minor changes in seismic P-wave velocity measurements and micro-CT imaging; the latter provided direct evidence of sparsely distributed calcium carbonate precipitation. Ion exchange processes promoted through NH{sub 4}{sup

  18. Amorphous calcium carbonate precipitation by cellular biomineralization in mantle cell cultures of Pinctada fucata.

    Directory of Open Access Journals (Sweden)

    Liang Xiang

    Full Text Available The growth of molluscan shell crystals is generally thought to be initiated from the extrapallial fluid by matrix proteins, however, the cellular mechanisms of shell formation pathway remain unknown. Here, we first report amorphous calcium carbonate (ACC precipitation by cellular biomineralization in primary mantle cell cultures of Pinctada fucata. Through real-time PCR and western blot analyses, we demonstrate that mantle cells retain the ability to synthesize and secrete ACCBP, Pif80 and nacrein in vitro. In addition, the cells also maintained high levels of alkaline phosphatase and carbonic anhydrase activity, enzymes responsible for shell formation. On the basis of polarized light microscopy and scanning electron microscopy, we observed intracellular crystals production by mantle cells in vitro. Fourier transform infrared spectroscopy and X-ray diffraction analyses revealed the crystals to be ACC, and de novo biomineralization was confirmed by following the incorporation of Sr into calcium carbonate. Our results demonstrate the ability of mantle cells to perform fundamental biomineralization processes via amorphous calcium carbonate, and these cells may be directly involved in pearl oyster shell formation.

  19. Calcium carbonate scaling in seawater desalination by ammonia-carbon dioxide forward osmosis: Mechanism and implications

    KAUST Repository

    Li, Zhenyu

    2015-02-07

    Forward osmosis (FO) is an osmotically driven membrane process, where the membrane separates a draw solution (DS) with high salinity from a feed solution (FS) with low salinity. There can be a counter direction flow of salt (i.e., salt leakage) that may interact with the water flux through the FO membrane. For the first time reported, this study describes a new calcium carbonate scaling phenomenon in the seawater FO desalination process using ammonium bicarbonate as the DS. The scaling on the membrane surface at the feed side is caused by the interaction between an anion reversely diffused from the DS and a cation present in the FS, causing a significant decline of the water flux. The composition of the scaling layer is dominated by the solubility (represented as solubility product constant, Ksp) of salt formed by the paired anion and cation. Membrane surface morphology plays a crucial role in the reversibility of the scaling. If the scaling occurs on the active layer of the FO membrane, hydraulic cleaning (increasing crossflow velocity) efficiency to restore the water flux is up to 82%. When scaling occurs on the support layer of the FO membrane, the hydraulic cleaning efficiency is strongly reduced, with only 36% of the water flux recovered. The present study reveals the risk of scaling induced by the interaction of feed solute and draw solute, which is different from the scaling caused by the supersaturation in reverse osmosis and other FO studies reported. The scaling investigated in this study can occur with a very low solute concentration at an early stage of the FO process. This finding provides an important implication for selection of draw solution and development of new membranes in the FO process.

  20. Fractional Absorption of Active Absorbable Algal Calcium (AAACa and Calcium Carbonate Measured by a Dual Stable-Isotope Method

    Directory of Open Access Journals (Sweden)

    Steven A. Abrams

    2010-07-01

    Full Text Available With the use of stable isotopes, this study aimed to compare the bioavailability of active absorbable algal calcium (AAACa, obtained from oyster shell powder heated to a high temperature, with an additional heated seaweed component (Heated Algal Ingredient, HAI, with that of calcium carbonate. In 10 postmenopausal women volunteers aged 59 to 77 years (mean ± S.D., 67 ± 5.3, the fractional calcium absorption of AAACa and CaCO3 was measured by a dual stable isotope method. 44Ca-enriched CaCO3 and AAACa were administered in all subjects one month apart. After a fixed-menu breakfast and pre-test urine collection (Urine 0, 42Ca-enriched CaCl2 was intravenously injected, followed by oral administration of 44Ca-enriched CaCO3 without carrier 15 minutes later, and complete urine collection for the next 24 hours (Urine 24. The fractional calcium absorption was calculated as the ratio of Augmentation of 44Ca from Urine 0 to Urine 24/ augmentation of 42Ca from Urine 0 to Urine 24. Differences and changes of 44Ca and 42Ca were corrected by comparing each with 43Ca. Fractional absorption of AAACa (mean ± S.D., 23.1 ± 6.4, was distinctly and significantly higher than that of CaCO3 (14.7 ± 6.4; p = 0.0060 by paired t-test. The mean fractional absorption was approximately 1.57-times higher for AAACa than for CaCO3. The serum 25(OH vitamin D level was low (mean ± S.D., 14.2 ± 4.95 ng/ml, as is common in this age group in Japan. Among the parameters of the bone and mineral metabolism measured, none displayed a significant correlation with the fractional absorption of CaCO3 and AAACa. Higher fractional absorption of AAACa compared with CaCO3 supports previous reports on the more beneficial effect of AAACa than CaCO3 for osteoporosis.

  1. Tamarind (Tamarindus indica) fruit shell carbon: A calcium-rich promising adsorbent for fluoride removal from groundwater

    Energy Technology Data Exchange (ETDEWEB)

    Sivasankar, V., E-mail: vsivasankar@tce.edu [Department of Chemistry, Thiagarajar College of Engineering (Autonomous), Madurai 625015, Tamil Nadu (India); Rajkumar, S. [Department of Chemistry, Thiagarajar College of Engineering (Autonomous), Madurai 625015, Tamil Nadu (India); Murugesh, S. [Department of Chemistry, SACS M.A.V.M.M. Engineering College, Madurai 625301, Tamil Nadu (India); Darchen, A. [UMR CNRS No. 6226 Sciences Chimiques de Rennes, ENSCR, Avenue du General Leclerc, CS 50837, 35708 Rennes, Cedex 7 (France)

    2012-07-30

    Highlights: Black-Right-Pointing-Pointer The carbonization of Tamarind fruit shell improved its defluoridation efficiency. Black-Right-Pointing-Pointer Calcium carbonate particles were involved in the defluoridation process. Black-Right-Pointing-Pointer Adsorbent dose, pH, and fluoride concentration showed significant effects. Black-Right-Pointing-Pointer Maximum adsorption of fluoride was achieved at pH 7-8. Black-Right-Pointing-Pointer Prepared carbons were efficient in treating three natural waters. - Abstract: Tamarindus indica fruit shells (TIFSs) are naturally calcium rich compounds. They were impregnated with ammonium carbonate and then carbonized, leading to ammonium carbonate activated ACA-TIFS carbon. The resulting materials and carbon arising from virgin fruit shells V-TIFS were characterized and assayed as adsorbent for the removal of fluoride anions from groundwater. The fluoride scavenging ability of TIFS carbons was due to naturally dispersed calcium compounds. X-ray diffraction (XRD) showed that TIFS carbon contained a mixture of calcium oxalate and calcium carbonate. Batch studies on the fluoride removal efficiency of TIFS carbons with respect to contact time, pH, initial fluoride concentration, and co-ion interference were conducted. Applicability of various kinetic models (viz., pseudo-first-order, pseudo-second-order, intra-particle diffusion and Elovich) and sorption isotherms were tested for batch techniques. The fluoride removal capacity of TIFS carbons was found to be 91% and 83% at a pH of 7.05 for V-TIFS and ACA-TIFS carbons, respectively. The practical applicability of TIFS carbons using groundwater samples was approved. The fluoride removal was greater in groundwater without hydrogen carbonate ions than those containing these ions. The characterizations of fluoride unloaded and loaded TIFS carbons were done by SEM and XRD studies.

  2. High conductivity transparent carbon nanotube films deposited from superacid

    Energy Technology Data Exchange (ETDEWEB)

    Hecht, David S; Lee, Roland; Hu Liangbing [Unidym Incorporated, 1244 Reamwood Drive, Sunnyvale, CA 94089 (United States); Heintz, Amy M; Moore, Bryon; Cucksey, Chad; Risser, Steven, E-mail: dhecht@gmail.com [Battelle, 505 King Avenue, Columbus, OH 43201 (United States)

    2011-02-18

    Carbon nanotubes (CNTs) were deposited from a chlorosulfonic superacid solution onto PET substrates by a filtration/transfer method. The sheet resistance and transmission (at 550 nm) of the films were 60 {Omega}/sq and 90.9% respectively, which corresponds to a DC conductivity of 12 825 S cm{sup -1} and a DC/optical conductivity ratio of 64.1. This is the highest DC conductivity reported for CNT thin films to date, and attributed to both the high quality of the CNT material and the exfoliation/doping by the superacid. This work demonstrates that CNT transparent films have not reached the conductivity limit; continued improvements will enable these films to be used as the transparent electrode for applications in solid state lighting, LCD displays, touch panels, and photovoltaics.

  3. High conductivity transparent carbon nanotube films deposited from superacid.

    Science.gov (United States)

    Hecht, David S; Heintz, Amy M; Lee, Roland; Hu, Liangbing; Moore, Bryon; Cucksey, Chad; Risser, Steven

    2011-02-18

    Carbon nanotubes (CNTs) were deposited from a chlorosulfonic superacid solution onto PET substrates by a filtration/transfer method. The sheet resistance and transmission (at 550 nm) of the films were 60 Ω/sq and 90.9% respectively, which corresponds to a DC conductivity of 12,825 S cm(-1) and a DC/optical conductivity ratio of 64.1. This is the highest DC conductivity reported for CNT thin films to date, and attributed to both the high quality of the CNT material and the exfoliation/doping by the superacid. This work demonstrates that CNT transparent films have not reached the conductivity limit; continued improvements will enable these films to be used as the transparent electrode for applications in solid state lighting, LCD displays, touch panels, and photovoltaics.

  4. Synthesis of Calcium(II) Amidinate Precursors for Atomic Layer Deposition through a Redox Reaction between Calcium and Amidines.

    Science.gov (United States)

    Kim, Sang Bok; Yang, Chuanxi; Powers, Tamara; Davis, Luke M; Lou, Xiabing; Gordon, Roy G

    2016-08-22

    We have prepared two new Ca(II) amidinates, which comprise a new class of ALD precursors. The syntheses proceed by a direct reaction between Ca metal and the amidine ligands in the presence of ammonia. Bis(N,N'-diisopropylformamidinato)calcium(II) (1) and bis(N,N'-diisopropylacetamidinato)calcium(II) (2) adopt dimeric structures in solution and in the solid state. X-ray crystallography revealed asymmetry in one of the bridging ligands to afford the structure [(η(2) -L)Ca(μ-η(2) :η(2) -L)(μ-η(2) :η(1) -L)Ca(η(2) -L)]. These amidinate complexes showed unprecedentedly high volatility as compared to the widely employed and commercially available Ca(II) precursor, [Ca3 (tmhd)6 ]. In CaS ALD with 1 and H2 S, the ALD window was approximately two times wider and lower in temperature by about 150 °C than previously reported with [Ca3 (tmhd)6 ] and H2 S. Complexes 1 and 2, with their excellent volatility and thermal stability (up to at least 350 °C), are the first homoleptic Ca(II) amidinates suitable for use as ALD precursors.

  5. Calcium Carbonate Crystal Growth in Porous Media, in the presence of Water Miscible and Non-Miscible Organic Fluids

    Science.gov (United States)

    Jaho, Sofia; Sygouni, Varvara; Paraskeva, Christakis A.

    2015-04-01

    The deposition of sparingly soluble salts (scaling) within porous media is a major problem encountered in many industrial and environmental applications. In the oil industry scaling causes severe operational malfunctions and, therefore, increasing the total operating and maintenance cost [1]. The most common types of sparingly soluble salts located in oil fields include carbonate and sulfate salts of calcium, strondium and barium[1,2]. Multiple phase flow and tubing surface properties are some of the factors affecting scale formation [3]. The main purpose of the present work was the investigation of the precipitation mechanisms of calcium carbonate (CaCO3) through in situ mixing of two soluble salt solutions in a flow granular medium, in the presence of water miscible organic fluid (ethylene glycol) or non-miscible organic fluid (n-dodecane). All series of experiments were carried out in a two dimensional porous medium made of Plexiglas. For all solutions used in the experiments, the contact angles with the surface of the porous medium and the interfacial tensions were measured. During the experiments, the calcium carbonate crystal growth was continuously monitored and recorded through an optical microscope equipped with a digital programmed video camera. The snap-shots were taken within specific time intervals and their detailed procession gave information concerning the crystal growth rate and kinetics. The pH of the effluent was measured and fluids samples were collected for calcium analysis using Atomic Absorption Spectroscopy (AAS). In all experiments effluent calcium concentration decreased as a function of time, suggesting that CaCO3 precipitation took place inside the porous medium. Crystals of the precipitated salt were identified using Infrared Spectroscopy (IR) and the morphology of the crystals was examined using Scanning Electron Microscopy (SEM). The induction time for precipitation of CaCO3 crystals in the presence of n-dodecane was significantly

  6. Pronounced carbonate deposition in the Early Triassic Dienerian substage: Who was the carbonate producer?

    Science.gov (United States)

    Horacek, Micha; Brandner, Rainer

    2014-05-01

    At the Late Permian Mass Extinction (LPME) most marine carbonate producers were heavily affected or even terminated. After the event in several sections a "boundary clay" was deposited and in the Griesbachian microbialites have been reported from many marine sections, however, without causing substantial thicknesses. The Dienerian in many Tethyan sections, though, is characterized by a huge increase in sedimentation rate due to the deposition of limestone mud with only minor amounts of siliciclastic input. This is in contrast to the still missing "usual" (skeletal) carbonate producers that have not yet re-appeared after the extinction, and also in contrast to a steeply and constantly rising marine Sr-isotope curve. To us this pattern indicates short timed intense post-extinction acidification in some areas causing a strong decrease of carbonate precipitation and thus resulting in the sedimentation of the boundary clay. Post-extinction low sedimentation rate supported the extensive growth of microbialites, thrombolites and stromatolites on seafloors in the photic zone, resulting in the photosynthetic uptake of bicarbonate ions which induced carbonate biomineralisation within the microbial mats probably during still prevailing acidic ocean condition. In the Dienerian the ocean water pH must have returned to non-acidic conditions again due to biotic and probably mainly microbial activity, resulting in a thriving and carbonate precipitating planctic microbial community producing huge amounts of microcrystalline carbonate mud. As some sections already in the Griesbachian feature substantial accumulations of carbonate mud layers, there acidification might have lasted only for a shorter period. Burial of the mainly microbial biomass probably also resulted in the positive 13C isotope curve trend from the Griesbachian to the Dienerian-Smithian boundary. Our interpretation identifies the (marine) microbial community as one of the important and THE biotic factor influencing

  7. Submesothelial deposition of carbon nanoparticles after toner exposition: Case report

    Directory of Open Access Journals (Sweden)

    Philippou Stathis

    2010-12-01

    Full Text Available Abstract Inhalation of carbon nanoparticles (CNP from toner dust has been shown to have impact on the respiratory health of persons exposed. Office printers are known emitters of CNP. We report about a female open office worker who developed weight loss and diarrhoea. Laparoscopy done for suspected endometriosis surprisingly revealed black spots within the peritoneum. Submesothelial aggregates of CNP with a diameter of 31-67 nm were found by scanning and transmission electron microscopy in these tissue specimens. Colon biopsies showed inflammatory bowel disease with typically signs of Crohn disease, but no dust deposits. Transport of CNP via lymphatic and blood vessels after inhalation in the lungs has to be assumed. In this case respiratory symptoms were not reported, therefore no lung function tests were done. We have shown that workers with toner dust exposure from laser printers can develop submesothelial deposition of CNP in the peritoneum. Impact of toner dust exposure on the respiratory health of office workers, as suspected in other studies, has to be evaluated further.

  8. Anthropogenic nitrogen deposition enhances carbon sequestration in boreal soils.

    Science.gov (United States)

    Maaroufi, Nadia I; Nordin, Annika; Hasselquist, Niles J; Bach, Lisbet H; Palmqvist, Kristin; Gundale, Michael J

    2015-08-01

    It is proposed that carbon (C) sequestration in response to reactive nitrogen (Nr ) deposition in boreal forests accounts for a large portion of the terrestrial sink for anthropogenic CO2 emissions. While studies have helped clarify the magnitude by which Nr deposition enhances C sequestration by forest vegetation, there remains a paucity of long-term experimental studies evaluating how soil C pools respond. We conducted a long-term experiment, maintained since 1996, consisting of three N addition levels (0, 12.5, and 50 kg N ha(-1) yr(-1) ) in the boreal zone of northern Sweden to understand how atmospheric Nr deposition affects soil C accumulation, soil microbial communities, and soil respiration. We hypothesized that soil C sequestration will increase, and soil microbial biomass and soil respiration will decrease, with disproportionately large changes expected compared to low levels of N addition. Our data showed that the low N addition treatment caused a non-significant increase in the organic horizon C pool of ~15% and a significant increase of ~30% in response to the high N treatment relative to the control. The relationship between C sequestration and N addition in the organic horizon was linear, with a slope of 10 kg C kg(-1) N. We also found a concomitant decrease in total microbial and fungal biomasses and a ~11% reduction in soil respiration in response to the high N treatment. Our data complement previous data from the same study system describing aboveground C sequestration, indicating a total ecosystem sequestration rate of 26 kg C kg(-1) N. These estimates are far lower than suggested by some previous modeling studies, and thus will help improve and validate current modeling efforts aimed at separating the effect of multiple global change factors on the C balance of the boreal region.

  9. Filtered pulsed cathodic arc deposition of fullerene-like carbon and carbon nitride films

    Science.gov (United States)

    Tucker, Mark D.; Czigány, Zsolt; Broitman, Esteban; Näslund, Lars-Åke; Hultman, Lars; Rosen, Johanna

    2014-04-01

    Carbon and carbon nitride films (CNx, 0 ≤ x ≤ 0.26) were deposited by filtered pulsed cathodic arc and were investigated using transmission electron microscopy and X-ray photoelectron spectroscopy. A "fullerene-like" (FL) structure of ordered graphitic planes, similar to that of magnetron sputtered FL-CNx films, was observed in films deposited at 175 °C and above, with N2 pressures of 0 and 0.5 mTorr. Higher substrate temperatures and significant nitrogen incorporation are required to produce similar FL structure by sputtering, which may, at least in part, be explained by the high ion charge states and ion energies characteristic of arc deposition. A gradual transition from majority sp3-hybridized films to sp2 films was observed with increasing substrate temperature. High elastic recovery, an attractive characteristic mechanical property of FL-CNx films, is evident in arc-deposited films both with and without nitrogen content, and both with and without FL structure.

  10. Filtered pulsed cathodic arc deposition of fullerene-like carbon and carbon nitride films

    Energy Technology Data Exchange (ETDEWEB)

    Tucker, Mark D., E-mail: martu@ifm.liu.se; Broitman, Esteban; Näslund, Lars-Åke; Hultman, Lars; Rosen, Johanna [Thin Film Physics Division, Department of Physics, Chemistry and Biology (IFM), Linköping University, SE-58183 Linköping (Sweden); Czigány, Zsolt [Institute for Technical Physics and Materials Science, RCNS, Hungarian Academy of Sciences, P.O. Box 49, H-1525 Budapest (Hungary)

    2014-04-14

    Carbon and carbon nitride films (CN{sub x}, 0 ≤ x ≤ 0.26) were deposited by filtered pulsed cathodic arc and were investigated using transmission electron microscopy and X-ray photoelectron spectroscopy. A “fullerene-like” (FL) structure of ordered graphitic planes, similar to that of magnetron sputtered FL-CN{sub x} films, was observed in films deposited at 175 °C and above, with N{sub 2} pressures of 0 and 0.5 mTorr. Higher substrate temperatures and significant nitrogen incorporation are required to produce similar FL structure by sputtering, which may, at least in part, be explained by the high ion charge states and ion energies characteristic of arc deposition. A gradual transition from majority sp{sup 3}-hybridized films to sp{sup 2} films was observed with increasing substrate temperature. High elastic recovery, an attractive characteristic mechanical property of FL-CN{sub x} films, is evident in arc-deposited films both with and without nitrogen content, and both with and without FL structure.

  11. Initial deposition of calcium phosphate ceramic on polyethylene and polydimethylsiloxane by rf magnetron sputtering deposition: the interface chemistry.

    NARCIS (Netherlands)

    Feddes, B.; Wolke, J.G.C.; Vredenberg, A.M.; Jansen, J.A.

    2004-01-01

    Calcium phosphate (CaP) coatings are well known for their bioactive nature. CaP coated polymeric materials can be used as implant material. For this, a strong adhesion between the coating and substrate is necessary. Because the chemical structure of the interface plays an important role in the coati

  12. Lithium and calcium carbides with polymeric carbon structures.

    Science.gov (United States)

    Benson, Daryn; Li, Yanling; Luo, Wei; Ahuja, Rajeev; Svensson, Gunnar; Häussermann, Ulrich

    2013-06-01

    We studied the binary carbide systems Li2C2 and CaC2 at high pressure using an evolutionary and ab initio random structure search methodology for crystal structure prediction. At ambient pressure Li2C2 and CaC2 represent salt-like acetylides consisting of C2(2-) dumbbell anions. The systems develop into semimetals (P3m1-Li2C2) and metals (Cmcm-Li2C2, Cmcm-CaC2, and Immm-CaC2) with polymeric anions (chains, layers, strands) at moderate pressures (below 20 GPa). Cmcm-CaC2 is energetically closely competing with the ground state structure. Polyanionic forms of carbon stabilized by electrostatic interactions with surrounding cations add a new feature to carbon chemistry. Semimetallic P3m1-Li2C2 displays an electronic structure close to that of graphene. The π* band, however, is hybridized with Li-sp states and changed into a bonding valence band. Metallic forms are predicted to be superconductors. Calculated critical temperatures may exceed 10 K for equilibrium volume structures.

  13. The effect of glycine on the growth of calcium carbonate in alkaline silica gel

    Science.gov (United States)

    Gan, Xiong; He, Kunhuan; Qian, Baosong; Deng, Qin; Lu, Laixian; Wang, Yun

    2017-01-01

    Calcium carbonate was crystallized in alkaline silica gel with the presence of glycine. The crystallization proceeded with a counterdiffusion method by the reaction of calcium chloride and sodium carbonate. Optical microscopy observation showed a significant effect of glycine on the morphology control of calcite crystals. When the initial concentration of glycine was high enough (10 mg/mL, 20 mg/mL), spherical vaterite particles formed in alkaline silica gel concomitantly together with dumbbell shaped calcite particles. The in situ study by micro-Raman spectroscopy demonstrated that both vaterite and the concomitant calcite were stable phases during their growth processes since the initial appearance. A possible mechanism has been discussed to emphasize the effect of glycine on the nucleation of vaterite and the morphological control of calcite.

  14. Comparative study of calcium alginate, activated carbon, and their composite beads on methylene blue adsorption.

    Science.gov (United States)

    Hassan, A F; Abdel-Mohsen, A M; Fouda, Moustafa M G

    2014-02-15

    Three adsorbents, calcium alginate beads (AB), sodium hydroxide activated carbon based coconut shells (C), and calcium alginate/activated carbon composite beads (ACB) were prepared. Their textural properties were characterized by N2-adsorption at -196°C and scanning electron microscopy. The porosity, surface area and total pore volume of C>ACB>AB, but AB adsorbent was more acidic function groups more than the other adsorbents. Adsorption experiments were conducted to examine the effects of adsorbent dosage, pH, time, temperature and initial concentration of methylene blue. Methylene blue adsorption on C, AB and ACB was observed at pH>6 to avoid the competition of H(+). The amount of dye adsorbed increases as the adsorbent dosage increase. Adsorption of dye follows pseudo-second order mechanism. Thermodynamic studies show spontaneous and endothermic nature of the overall adsorption process.

  15. Dehydration and crystallization of amorphous calcium carbonate in solution and in air.

    Science.gov (United States)

    Ihli, Johannes; Wong, Wai Ching; Noel, Elizabeth H; Kim, Yi-Yeoun; Kulak, Alexander N; Christenson, Hugo K; Duer, Melinda J; Meldrum, Fiona C

    2014-01-01

    The mechanisms by which amorphous intermediates transform into crystalline materials are poorly understood. Currently, attracting enormous interest is the crystallization of amorphous calcium carbonate, a key intermediary in synthetic, biological and environmental systems. Here we attempt to unify many contrasting and apparently contradictory studies by investigating this process in detail. We show that amorphous calcium carbonate can dehydrate before crystallizing, both in solution and in air, while thermal analyses and solid-state nuclear magnetic resonance measurements reveal that its water is present in distinct environments. Loss of the final water fraction--comprising less than 15% of the total--then triggers crystallization. The high activation energy of this step suggests that it occurs by partial dissolution/recrystallization, mediated by surface water, and the majority of the particle then crystallizes by a solid-state transformation. Such mechanisms are likely to be widespread in solid-state reactions and their characterization will facilitate greater control over these processes.

  16. Effects of calcium gluconate on the utilization of magnesium and the nephrocalcinosis in rats fed excess dietary phosphorus and calcium.

    Science.gov (United States)

    Chonan, O; Takahashi, R; Kado, S; Nagata, Y; Kimura, H; Uchida, K; Watanuki, M

    1996-08-01

    The effects of calcium gluconate on the utilization of magnesium and nephrocalcinosis in male Wistar rats made magnesium-deficient by adding excess dietary phosphorus (1.195 g of phosphorus/100 g of diet) and calcium (1.04 g of calcium/100 g of diet) were compared with the effects of calcium carbonate. The effects of dietary magnesium concentration on the magnesium status and nephrocalcinosis were also examined. Adding excess dietary phosphorus and calcium decreased the apparent magnesium absorption ratios and the concentrations of magnesium in the serum and femur and increased the deposition of calcium in the kidney, and the low magnesium condition (0.024 g of magnesium/100 g of diet) aggravated the deposition of calcium and the low magnesium status. The apparent magnesium absorption ratios and femur magnesium concentration in the rats fed a calcium gluconate diet (an equimolar mixture of calcium gluconate and calcium carbonate was used as a source of calcium) were significantly higher than in the rats fed a calcium carbonate diet (only calcium carbonate was used as a source of calcium), irrespective of dietary magnesium concentration. Dietary calcium gluconate lessened the accumulation of calcium in the kidney and increased the serum magnesium concentration compared with dietary calcium carbonate, when the rats were fed the normal magnesium diet (0.049 g of magnesium/100 g of diet) but not the low magnesium diet. We speculate that the increased utilization of magnesium by feeding the calcium gluconate diet to a limited extent prevented the low magnesium status and the severity of nephrocalcinosis caused by adding excess dietary phosphorus and calcium.

  17. Calcium Carbonate versus Sevelamer Hydrochloride as Phosphate Binders after Long-Term Disease Progression in 5/6 Nephrectomized Rats

    Directory of Open Access Journals (Sweden)

    Suvi Törmänen

    2014-01-01

    Full Text Available Our aim was to compare the effects of calcium carbonate and sevelamer-HCl treatments on calcium-phosphate metabolism and renal function in 5/6 nephrectomized (NX rats so that long-term disease progression preceded the treatment. After 15-week progression, calcium carbonate (3.0%, sevelamer-HCl (3.0%, or control diets (0.3% calcium were given for 9 weeks. Subtotal nephrectomy reduced creatinine clearance (−40%, plasma calcidiol (−25%, and calcitriol (−70% and increased phosphate (+37%, parathyroid hormone (PTH (11-fold, and fibroblast growth factor-23 (FGF-23 (4-fold. In NX rats, calcium carbonate diet increased plasma (+20% and urinary calcium (6-fold, reduced plasma phosphate (−50% and calcidiol (−30%, decreased creatinine clearance (−35% and FGF 23 (−85%, and suppressed PTH without influencing blood pH. In NX rats, sevelamer-HCl increased urinary calcium (4-fold and decreased creatinine clearance (−45%, PTH (−75%, blood pH (by 0.20 units, plasma calcidiol (−40%, and calcitriol (−65%. Plasma phosphate and FGF-23 were unchanged. In conclusion, when initiated after long-term progression of experimental renal insufficiency, calcium carbonate diet reduced plasma phosphate and FGF-23 while sevelamer-HCl did not. The former induced hypercalcemia, the latter induced acidosis, while both treatments reduced vitamin D metabolites and deteriorated renal function. Thus, delayed initiation influences the effects of these phosphate binders in remnant kidney rats.

  18. Dual ion beam deposition of carbon films with diamondlike properties

    Science.gov (United States)

    Mirtich, M. J.; Swec, D. M.; Angus, J. C.

    1984-01-01

    A single and dual ion beam system was used to generate amorphous carbon films with diamond like properties. A methane/argon mixture at a molar ratio of 0.28 was ionized in the low pressure discharge chamber of a 30-cm-diameter ion source. A second ion source, 8 cm in diameter was used to direct a beam of 600 eV Argon ions on the substrates (fused silica or silicon) while the deposition from the 30-cm ion source was taking place. Nuclear reaction and combustion analysis indicate H/C ratios for the films to be 1.00. This high value of H/C, it is felt, allowed the films to have good transmittance. The films were impervious to reagents which dissolve graphitic and polymeric carbon structures. Although the measured density of the films was approximately 1.8 gm/cu cm, a value lower than diamond, the films exhibited other properties that were relatively close to diamond. These films were compared with diamondlike films generated by sputtering a graphite target.

  19. Capillarity creates single-crystal calcite nanowires from amorphous calcium carbonate.

    Science.gov (United States)

    Kim, Yi-Yeoun; Hetherington, Nicola B J; Noel, Elizabeth H; Kröger, Roland; Charnock, John M; Christenson, Hugo K; Meldrum, Fiona C

    2011-12-23

    Single-crystal calcite nanowires are formed by crystallization of morphologically equivalent amorphous calcium carbonate (ACC) particles within the pores of track etch membranes. The polyaspartic acid stabilized ACC is drawn into the membrane pores by capillary action, and the single-crystal nature of the nanowires is attributed to the limited contact of the intramembrane ACC particle with the bulk solution. The reaction environment then supports transformation to a single-crystal product.

  20. Metal scavenging by calcium carbonate at the Eyjafjallajökull volcano

    DEFF Research Database (Denmark)

    Olsson, J.; Stipp, S. L S; Makovicky, E.

    2014-01-01

    in the Icelandic river, Hvanná, in the vicinity of the volcano. The river water emerged from under the lava flow and was heavily charged with cations and dissolved CO2. The concentration of the major dissolved constituents was: dissolved inorganic carbon (DIC), 33.08mM; calcium, 6.17mM; magnesium, 4.27mM; sodium...

  1. Obtainment of calcium carbonate from mussels shell; Obtencao de carbonato de calcio a partir de conchas de mariscos

    Energy Technology Data Exchange (ETDEWEB)

    Hamester, M.R.R.; Becker, D., E-mail: michele.rosa@sociesc.org.b [Sociedade Educacional de Santa Catarina (SOCIESC), Joinville, SC (Brazil). Mestrado Profissional em Engenharia Mecanica

    2010-07-01

    The mussels and oyster shell are discarded at environment, and this accumulation is causing negative consequences to ecosystem. Calcium carbonate is main constituent of the shell chemical composition. Aiming to reduce environmental aggression and generate income to shellfish producer, there was the possibility of using these shells as an alternative to commercial calcium carbonate. For this physics, chemicals and thermal properties were evaluated, using X-ray fluorescence, thermogravimetric analysis, size distribution, abrasiveness and scanning electronic microscopy. The results indicate that mussels shells have an initial degradation temperature higher than commercial calcium carbonate e same lost weight behavior and 95% of shell chemical composition is calcium carbonate. The sample size distribution was influenced by grinding condition and time as well as its abrasiveness. (author)

  2. REINFORCEMENT OF POLYDIMETHYLSILOXANE NETWORKS BY NANO-CALCIUM CARBONATE

    Institute of Scientific and Technical Information of China (English)

    Ya Peng; Rong-ni Du; Qiang Fu; Yue-lin Wang

    2005-01-01

    Although a number of investigations have been devoted to the analysis of silica or carbon black filled elastomer networks, little work has been done on the reinforcement of CaCO3 filled elastomer network. In this work, the reinforcement of polydimethylsiloxane (PDMS) network by using CaCO3 nano-particles was investigated. We have found a simultaneous increase of tensile strength, modulus and elongation with the increase in nano-CaCO3 content, which suggests that nanoCaCO3 panicles can indeed be used as a reinforcing agent, just like silica or carbon black. Interestingly, the tensile strength,modulus and elongation were seen to leave off for the first time when the content of nano-CaCO3 paticles reaches to 80%.PDMS also showed an enhanced elastic modulus and storage modulus with the increase in nano-CaCO3 content, particularly for samples with high nano-CaCO3 content. SEM was used to investigate the dispersion of the filler in PDMS matrix. A better dispersion was found for samples with high nano-CaCO3 content. A great increase of viscosity was found for samples with higher filler content, which is considered to be the reason for the good dispersion thus the reinforcement, because high viscosity will be helpful for breaking the agglomerates of fillers into small size particles under effect of shear. Our work provides a new way for the reinforcement of elastomer by using an adequate amount of nano-CaCO3 particles instead of a small quantity of silica, which is not only economically cheap but also very effective.

  3. Synthesis and Characterisation of Calcium Carbonate Aragonite Nanocrystals from Cockle Shell Powder (Anadara granosa

    Directory of Open Access Journals (Sweden)

    Abdullahi Shafiu Kamba

    2013-01-01

    Full Text Available The synthesis of pure calcium carbonate nanocrystals using a high pressure homogeniser (HPH via a microemulsion system produced uniform nanosized particles, which were characterised using transmission electron microscopy (TEM, field-emission scanning electron microscopy (FESEM, X-ray diffraction (XRD, Fourier transform infrared spectroscopy (FTIR, and thermogravimetric analysis (TGA. The identified particles were aragonite polymorphs with a rod shape and were approximately 50 nm in size. The aragonite polymorph of calcium carbonate was prepared from biogenic materials, cockle shells, and exhibited unique characteristics (i.e., a higher density than that of calcite, which makes it biocompatible and potentially suitable for applications in the medical, pharmaceutical, cosmetic, and paint industries. The methods adopted and the nonionic surfactant used in the synthesis of calcium carbonate nanocrystalline aragonite polymorphs were environmentally friendly and can be scaled up for industrial production. The sources are naturally available materials that are by-products of the seafood industry, which offers an opportunity for exploitation in numerous industrial applications.

  4. Characterization of calcium carbonate obtained from oyster and mussel shells and incorporation in polypropylene

    Directory of Open Access Journals (Sweden)

    Michele Regina Rosa Hamester

    2012-04-01

    Full Text Available There is a high content of calcium carbonate in mussel and oyster shells, which can be used in the formulation of medicine, in construction or as filler in polymer materials. This work has as its main objective to obtain calcium carbonate from mussel and oyster shells and used as filler in polypropylene compared their properties with polypropylene and commercial calcium carbonate composites. The shellfish was milling and heated at 500 ºC for 2 hours. The powder obtained from shellfish were characterized by scanning electron microscopy (SEM, X-ray fluorescence, particle size distribution and abrasiveness and compared with commercial CaCO3 and mixed with polypropylene. The thermal and mechanical properties of polypropylene with CaCO3 obtained from oyster and mussel shells and with commercial CaCO3 were analysed. The results showed that CaCO3­ can be obtained from oyster and mussel shell and is technically possible to replace the commercial CaCO3 for that obtained from the shells of shellfish in polypropylene composites.

  5. Compaction of functionalized calcium carbonate, a porous and crystalline microparticulate material with a lamellar surface.

    Science.gov (United States)

    Stirnimann, Tanja; Atria, Susanna; Schoelkopf, Joachim; Gane, Patrick A C; Alles, Rainer; Huwyler, Jörg; Puchkov, Maxim

    2014-05-15

    In the present study, we aimed to characterize the compressibility and compactibility of the novel pharmaceutical excipient, functionalized calcium carbonate (FCC). We studied three FCC modifications and compared the values for compressibility and compactibility with mannitol, microcrystalline cellulose (MCC), and ground calcium carbonate (CC 330) as well as mixtures of paracetamol and MCC or FCC at drug loads of 0%, 25%, 50%, 75%, and 100% (w/w). We used Heckel analysis, modified Heckel analysis, and Leuenberger analysis to characterize the compaction and compression behavior of the mixtures. Compaction analysis of FCC showed this material to markedly differ from ground calcium carbonate, exhibiting properties, i.e. plastic deformability, similar to those of MCC. This effect was attributed to the highly lamellar structure of FCC particles whose thickness is of the order of a single crystal unit cell. According to Leuenberger parameters, we concluded that FCC-based tablet formulations had mechanical properties equal or superior to those formulated with MCC. FCC tablets with high tensile strength were obtained already at low compressive pressures. Owing to these favorable properties (i.e. marked tensile strength and porosity), FCC promises to be suitable for the preparation of solid dosage forms.

  6. Bacillus megaterium mediated mineralization of calcium carbonate as biogenic surface treatment of green building materials.

    Science.gov (United States)

    Dhami, Navdeep Kaur; Reddy, M Sudhakara; Mukherjee, Abhijit

    2013-12-01

    Microbially induced calcium carbonate precipitation is a biomineralization process that has various applications in remediation and restoration of range of building materials. In the present study, calcifying bacteria, Bacillus megaterium SS3 isolated from calcareous soil was applied as biosealant to enhance the durability of low energy, green building materials (soil-cement blocks). This bacterial isolate produced high amounts of urease, carbonic anhydrase, extra polymeric substances and biofilm. The calcium carbonate polymorphs produced by B. megaterium SS3 were analyzed by scanning electron microscopy, confocal laser scanning microscopy, X-ray diffraction and Fourier transmission infra red spectroscopy. These results suggested that calcite is the most predominant carbonate formed by this bacteria followed by vaterite. Application of B. megaterium SS3 as biogenic surface treatment led to 40 % decrease in water absorption, 31 % decrease in porosity and 18 % increase in compressive strength of low energy building materials. From the present investigation, it is clear that surface treatment of building materials by B. megaterium SS3 is very effective and eco friendly way of biodeposition of coherent carbonates that enhances the durability of building materials.

  7. Growth rate and calcium carbonate accumulation of Halimeda macrolobaDecaisne (Chlorophyta: Halimedaceae in Thai waters

    Directory of Open Access Journals (Sweden)

    Jaruwan Mayakun

    2014-08-01

    Full Text Available Halimeda macroloba Decaisne can utilize the CO2 used for carbon fixation in photosynthesis and use bicarbonate as the main carbon source for calcification. Although Halimeda has been recognized as a carbon sink species, the calcium accumulation of Halimeda species in Thai waters remain poorly understood. In this study, the highest density of H. macroloba was 26 thalli/m2 and Halimeda quickly produced 1-2 new segments/thallus/day or 20.1 mg dry weight/thallus/day. Its calcium carbonate accumulation rate was 16.6 mg CaCO3 /thallus/day, or 82.46 % per thallus. In Thailand, however, only three scientific papers of growth rate and CaCO3 accumulation rate of H. macroloba have been found and collected. Of these records, the mean density was 26-104 thalli/m2 . The growth rate of H. macroloba was around 1-2 mg dry weight/day and the CaCO3 accumulation rate varied around 41-91%. Thus, Halimeda has a great potential to decrease the carbon dioxide concentration in the ocean.

  8. Contrasting histopathology and crystal deposits in kidneys of idiopathic stone formers who produce hydroxy apatite, brushite, or calcium oxalate stones.

    Science.gov (United States)

    Evan, Andrew P; Lingeman, James E; Worcester, Elaine M; Sommer, Andre J; Phillips, Carrie L; Williams, James C; Coe, Fredric L

    2014-04-01

    Our previous work has shown that stone formers who form calcium phosphate (CaP) stones that contain any brushite (BRSF) have a distinctive renal histopathology and surgical anatomy when compared with idiopathic calcium oxalate stone formers (ICSF). Here we report on another group of idiopathic CaP stone formers, those forming stone containing primarily hydroxyapatite, in order to clarify in what ways their pathology differs from BRSF and ICSF. Eleven hydroxyapatite stone formers (HASF) (2 males, 9 females) were studied using intra-operative digital photography and biopsy of papillary and cortical regions to measure tissue changes associated with stone formation. Our main finding is that HASF and BRSF differ significantly from each other and that both differ greatly from ICSF. Both BRSF and ICSF patients have significant levels of Randall's plaque compared with HASF. Intra-tubular deposit number is greater in HASF than BRSF and nonexistent in ICSF while deposit size is smaller in HASF than BRSF. Cortical pathology is distinctly greater in BRSF than HASF. Four attached stones were observed in HASF, three in 25 BRSF and 5-10 per ICSF patient. HASF and BRSF differ clinically in that both have higher average urine pH, supersaturation of CaP, and calcium excretion than ICSF. Our work suggests that HASF and BRSF are two distinct and separate diseases and both differ greatly from ICSF.

  9. Comparison of in vitro and in vivo tests for determination of availability of calcium from calcium carbonate tablets.

    Science.gov (United States)

    Whiting, S J; Pluhator, M M

    1992-10-01

    In vitro tests of calcium (Ca) availability and the oral Ca load test were conducted on eight brands of calcium carbonate (CaCO3) tablets (products A-H) each providing 500 mg Ca. Data were collected over three experiments with nine to 11 healthy premenopausal women testing two to four products. Subjects followed a low Ca diet (less than 10 mmol/day). On test mornings, fasting subjects collected baseline urine for 2 hours (-2 to 0 hours), then ingested the tablet with water. Urine was collected from 0 to 2 hours and 2 to 4 hours; for products E-H, urine was collected for an additional 2 hours (4 to 6 hours). Blood was sampled at hours 0, 4 and 6 during testing of products E and F. Three in vitro tests were run: the United States Pharmacopeia (USP) dissolution test, USP disintegration test, and a disintegration test using vinegar. Ca excretion rose significantly at hours 2 to 4 (p less than 0.05) compared to baseline for seven products. Ca excretion either fell or remained constant between hours 4 and 6. Serum Ca rose and serum parathyroid hormone fell at hour 4, compared to fasting values, suggesting that 4 hours represents peak response time. In vivo availability, measured as the incremental increase in Ca excretion (mmol/mmol creatinine) in hours 2 to 4 compared to baseline, did not correlate significantly with results of the USP dissolution test but did with results of either the USP disintegration test or the vinegar test.(ABSTRACT TRUNCATED AT 250 WORDS)

  10. Heterogeneous uptake and reactivity of formic acid on calcium carbonate particles: a Knudsen cell reactor, FTIR and SEM study.

    Science.gov (United States)

    Al-Hosney, Hashim A; Carlos-Cuellar, Sofia; Baltrusaitis, Jonas; Grassian, Vicki H

    2005-10-21

    The heterogeneous uptake and reactivity of formic acid (HCOOH), a common gas-phase organic acid found in the environment, on calcium carbonate (CaCO(3)) particles have been investigated using a Knudsen cell reactor, Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM). FTIR measurements show that the adsorption of formic acid on the surface of calcium carbonate results in the formation of calcium formate. Besides calcium formate, carbonic acid is also a reaction product under dry conditions (dry conditions and at low pressures, the initial uptake coefficient of formic acid on CaCO(3) particles is measured to be 3 +/- 1 x 10(-3) and decreases as the surface saturates with adsorbed products. The maximum surface coverage of formic acid under dry conditions is determined to be (3 +/- 1)x 10(14) molecules cm(-2). Under humidified conditions (RH >10%), adsorbed water on the surface of the carbonate particles participates in the surface reactivity of these particles, which results in the enhanced uptake kinetics and extent of reaction of this organic acid on CaCO(3) as well as opens up several new reaction pathways. These reaction pathways include: (i) the water-assisted dissociation of carbonic acid to CO(2) and H(2)O and (ii) the formation of calcium formate islands and crystallites, as evident by SEM images. The results presented here show that adsorbed water plays a potentially important role in the surface chemistry of gas-phase organic acids on calcium carbonate particles.

  11. Scientific Opinion on the safety assessment of the active substances, sodium erythorbate, sodium carbonate, sodium bicarbonate, iron sulphate, activated carbon, cellulose, calcium hydroxide, calcium chloride and water, for use as active system in food contact materials

    Directory of Open Access Journals (Sweden)

    EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF

    2014-02-01

    Full Text Available This scientific opinion of EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids deals with the safety assessment of the active substances sodium erythorbate, sodium carbonate, sodium bicarbonate, iron sulfate, activated carbon, cellulose, calcium hydroxide, calcium chloride and water, used in mixture which is packed into sachets for absorbing oxygen/carbon dioxide emitting from/into the headspace surrounding packed food. All substances of this formulation have been evaluated and approved for use as additives in plastic food contact materials or as food additives. No migration of calcium, iron and sodium ions was detected. No volatile organic compounds other than carbon dioxide were detected at the limit of detection of 0.5 μg/l. The CEF Panel concluded that the use of the substances sodium erythorbate, sodium carbonate, sodium bicarbonate, iron sulfate, activated carbon, cellulose, calcium hydroxide, calcium chloride and water does not raise a safety concern when used in oxygen absorber/carbon dioxide emitter systems, in sachets that prevent the physical release of their contents into the food. The sachets are to be placed in the headspace of the packaging and as such may come into occasional contact with the food, e.g. during handling. The sachet should not come into direct contact with liquid foods or foods that have and external aqueous liquid phase on the surface (liquid or exudates.

  12. Purifications of calcium carbonate and molybdenum oxide powders for neutrinoless double beta decay experiment, AMoRE

    Energy Technology Data Exchange (ETDEWEB)

    Park, HyangKyu [Center for Underground Physics, Institute for Basic Science, 70, Yuseong-daero 1689-gil, Yuseong-gu, Daejeon, Korea, 305-811 (Korea, Republic of)

    2015-08-17

    The AMoRE (Advanced Mo based Rare process Experiment) collaboration is going to use calcium molybdate crystals to search for neutrinoless double beta decay of {sup 100}Mo isotope. In order to make the crystal, we use calcium carbonate and molybdenum oxide powders as raw materials. Therefore it is highly necessary to reduce potential sources for radioactive backgrounds such as U and Th in the powders. In this talk, we will present our studies for purification of calcium carbonate and molybdenum oxide powders.

  13. Isotopic composition of carbon and oxygen of carbonates of oil and gas-bearing deposits of Western Siberia

    Energy Technology Data Exchange (ETDEWEB)

    Golyshev, S.I.; Cherepnin, A.V.; Rozhnev, A.N.

    1981-01-01

    There is measured the isotopic composition of carbon and oxygen in 129 samples of carbonates and carbonate cements of oil and gas-bearing Paleozoic and Mezozoic deposits of Western Siberia. The isotopic composition of samples of marine deposits varies from -1.2 to +6.1% for carbon and from 19.8 to 29.1% for oxygen and has a mean isotopic composition of 1.9 to 24.8%. Catagenetic processes lead to lightening of the isotopic composition of secondary carbonate on the average by 5% for carbon and 9% for oxygen. The most intense lightening of isotopic composition is observed in samples disposed near oil and gas deposits.

  14. Carbon molecular sieves from bituminous coal by controlled coke deposition

    Energy Technology Data Exchange (ETDEWEB)

    Vyas, S.N.; Patwardhan, S.R.; Gangadhar, B. (Indian Institute of Technology, Bombay (India). Dept. of Chemical Engineering)

    1992-01-01

    Carbon molecular sieves (CMS) and zeolites are widely used as microporous sieving solids for gas and liquid separations. However, due to hydrophobicity, better thermal stability, and neutrality in both acidic and alkaline media, CMSs have definite advantages over zeolites. In the present work, an effort has been made to develop suitable process conditions for synthesizing CMSs from the locally available bituminous coal. The coal was crushed, milled, and agglomerated with sulfate pulp waste liquor (SPWL) or coal-tar pitch (CTP) as the binders, and then carbonized in nitrogen atmosphere at 800{degree}C for about 60 minutes. In order to narrow down the pore mouth sizes, acetylene and benzene were each cracked separately at 800{degree}C to facilitate the deposition of coke on the char. Acetylene and benzene were cracked for 3 to 10 minutes, and 10 to 30 minutes, respectively. Acetylene cracked samples did not show good separation, probably because of over-coking in deeper locations. In contrast benzene cracked samples were found to be highly suitable for CO{sub 2}-CH{sub 4} separation. The best result (i.e. uptake ratio of 39.9) was obtained for feed benzene entrainment in N{sub 2} of 1.27 x 10{sup -4} g/ml, cracking time of 30 minutes, and this ratio was more than 10 times that of non-coked sample. CMS samples produced using SPWL as binder showed poor O{sub 2}/N{sub 2} uptake ratios throughout (1 to 1.5), whereas samples with CTP as binder showed far more encouraging results, the best uptake ratio being 5.5 for benzene-nitrogen feed stream containing 3.508 x 10{sup -4} g/ml benzene and 5 minutes cracking time. This ratio is about 5.5 times more than that of uncoked sample. 4 tabs., 10 figs., 17 refs.

  15. A unique laboratory test rig reduces the need for offshore tests to combat calcium naphthenate deposition in oilfield process equipment.

    Energy Technology Data Exchange (ETDEWEB)

    Mediaas, Heidi; Grande, Knut; Hustad, Britt-Marie; Hoevik, Kim Reidar; Kummernes, Hege; Nergaard, Bjoern; Vindstad, Jens Emil

    2006-03-15

    Producing and refining high-TAN crude oils introduces a number of challenges, among which calcium naphthenate deposition in process facilities is the most serious production issue. Until recently, the only option for studying chemicals and process parameters in order to prevent naphthenate deposition has been field tests. Statoil has now developed a small scale pilot plant where these experiments can be performed in the laboratory at Statoil's Research and Technology Center in Trondheim, Norway. The results from the pilot plant are in full agreement with the extensive naphthenate experience obtained from almost 9 years operation of the Heidrun oilfield. The design and operational procedures for this test facility are based on the recent discovery by Statoil and ConocoPhillips of the ARN acid. The ARN acid is a prerequisite for calcium naphthenate deposition. The new continuous flow pilot plant, the Naphthenate Rig, is used to develop new environmental friendly naphthenate inhibitors and to optimize process operating conditions. Since it operates on real crudes the need for field tests in qualifying new naphthenate inhibitors is reduced. To the best of our knowledge, the rig is the first of its kind in the world. (Author)

  16. Effects of Carbon Fiber Gas Pressure, Temperature and Deposition Distance on Thermo Fluids Phenomena in Vacuum Deposition Machine

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    A numerical analysis method (DSMC, Direct Simulation Monte Carlo)[l] was developed to simulate the molecular motion of rarefied gases. In the present paper, numerical approaches by the DSMC method have been carfled out. By the computation model of CC-40F carbon coater, the cylindrical deposition machine has axial symmetry; the flows inside the vacuum chamber were analyzed. The substrates were put on the bottom and the fiber near the ceiling in the computational domain. In the computational model, air and carbon molecules are working ones. The effects of the air gas pressure variation in the chamber, the effects of the deposition distance variation and the surface temperature variation of the carbon fiber on thermo fluids phenomena are discussed and visualized. Changing the number density of carbon and air, the temperature of the carbon and the velocity of the carbon in the chamber are discussed. With changing the surface temperature of the carbon fiber, qualitative assay of experiment and simulation result is in similar trend very well. The DSMC method is a forceful tool for the study of rarefied gas flow in vacuum deposition machine.

  17. Climate warming shifts carbon allocation from stemwood to roots in calcium-depleted spruce forests

    Science.gov (United States)

    Lapenis, Andrei Gennady; Lawrence, Gregory B.; Heim, Alexander; Zheng, Chengyang; Shortle, Walter

    2013-01-01

    Increased greening of northern forests, measured by the Normalized Difference Vegetation Index (NDVI), has been presented as evidence that a warmer climate has increased both net primary productivity (NPP) and the carbon sink in boreal forests. However, higher production and greener canopies may accompany changes in carbon allocation that favor foliage or fine roots over less decomposable woody biomass. Furthermore, tree core data throughout mid- and northern latitudes have revealed a divergence problem (DP), a weakening in tree ring responses to warming over the past half century that is receiving increasing attention, but remains poorly understood. Often, the same sites exhibit trend inconsistency phenomenon (TIP), namely positive, or no trends in growing season NDVI where negative trends in tree ring indexes are observed. Here we studied growth of two Norway spruce (Picea abies) stands in western Russia that exhibited both the DP and TIP but were subject to soil acidification and calcium depletion of differing timing and severity. Our results link the decline in radial growth starting in 1980 to a shift in carbon allocation from wood to roots driven by a combination of two factors: (a) soil acidification that depleted calcium and impaired root function and (b) earlier onset of the growing season that further taxed the root system. The latter change in phenology appears to act as a trigger at both sites to push trees into nutrient limitation as the demand for Ca increased with the longer growing season, thereby causing the shift in carbon allocation.

  18. Climate warming shifts carbon allocation from stemwood to roots in calcium-depleted spruce forests

    Science.gov (United States)

    Lapenis, Andrei; Lawrence, Gregory; Buyantuev, Alexander

    2015-04-01

    Increased greening of northern forests, measured by the Normalized Difference Vegetation Index (NDVI), has been presented as evidence that a warmer climate has increased both net primary productivity (NPP) and the carbon sink in boreal forests. However, higher production and greener canopies may accompany changes in carbon allocation that favor foliage or fine roots over less decomposable woody biomass. Furthermore, tree core data throughout mid- and northern latitudes have revealed a divergence problem (DP), a weakening in tree ring responses to warming over the past half century that is receiving increasing attention, but remains poorly understood. Often, the same sites exhibit trend inconsistency phenomenon (TIP), namely positive, or no trends in growing season NDVI where negative trends in tree ring indexes are observed. Here we studied growth of two Norway spruce (Picea abies) stands in western Russia that exhibited both the DP and TIP but were subject to soil acidification and calcium depletion of differing timing and severity. Our results link the decline in radial growth starting in 1980 to a shift in carbon allocation from wood to roots driven by a combination of two factors: (a) soil acidification that depleted calcium and impaired root function and (b) earlier onset of the growing season that further taxed the root system. The latter change in phenology appears to act as a trigger at both sites to push trees into nutrient limitation as the demand for Ca increased with the longer growing season, thereby causing the shift in carbon allocation.

  19. Effect of Temperature on Precipitation Rate of Calcium Carbonate Produced through Microbial Metabolic Process of Bio Materials

    Directory of Open Access Journals (Sweden)

    Prima Yane Putri

    2016-09-01

    Full Text Available Concrete is the most widely used construction material in civil engineering. But plain concrete is a brittle material and has little resistance to cracking. The cracking in concrete promotes deterioration such as the corrosion of reinforcing rebar, therefore, repair in filling the crack is often carried out. Recently, repair methods using bio-based materials associated with microbial metabolic processes leading to precipitation of calcium carbonate have been intensively studied. In this study, influencing factors on the precipitation rate depending on the constituents of bio-based material comprising yeast, glucose and calcium acetate mixed in tris buffer solution was examined for improving the rate of initial reactions. In addition, effect of temperature change on the amount of calcium carbonate precipitation was also investigated. The precipitates were identified by X-ray diffraction. It was shown that the increase of temperature lead to a change on calcium carbonate precipitation and caused the pH decrease under 7.0.

  20. 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.

  1. A Chemical Template for Synthesis of Molecular Sheets of Calcium Carbonate

    Science.gov (United States)

    Rianasari, Ina; Benyettou, Farah; Sharma, Sudhir Kumar; Blanton, Thomas; Kirmizialtin, Serdal; Jagannathan, Ramesh

    2016-05-01

    Inspired by the discovery of graphene and its unique properties, we focused our research to develop a scheme to create nacre like lamellar structures of molecular sheets of CaCO3 interleaved with an organic material, namely carbon. We developed a facile, chemical template technique, using a formulation of poly(acrylic) acid (PAA) and calcium acetate to create lamellar stacks of single crystal sheets of CaCO3, with a nominal thickness of 17 Å, the same as a unit-cell dimension for calcite (c-axis = 17.062 Å), interleaved with amorphous carbon with a nominal thickness of 8 Å. The strong binding affinity between carboxylate anions and calcium cations in the formulation was used as a molecular template to guide CaCO3 crystallization. Computational modeling of the FTIR spectra showed good agreement with experimental data and confirmed that calcium ions are bridged between polymer chains, resulting in a net-like polymer structure. The process readily lends itself to explore the feasibility of creating molecular sheets of other important inorganic materials and potentially find applications in many fields such as super capacitors and “low k di-electric” systems.

  2. Detection of lead ions in picomolar concentration range using underpotential deposition on silver nanoparticles-deposited glassy carbon electrodes.

    Science.gov (United States)

    Sivasubramanian, R; Sangaranarayanan, M V

    2011-09-30

    The efficacy of silver-deposited glassy carbon electrode for the determination of lead ions at the sub-nanomolar concentration ranges is investigated. The silver nanoparticles are electrodeposited on glassy carbon electrode using chronoamperometry and the electrode surface is characterized using SEM. Lead ions are detected in the region of underpotential deposition. The analysis is performed in square wave mode in the stripping voltammetry without the removal of oxygen. The detection limit of 10 pM has been obtained with a constant potential of -0.7 V during the electrodeposition step for a period of 50s. The interference of surfactants in the detection of lead ions is also studied.

  3. Preparation of Dispersed Platinum Nanoparticles on a Carbon Nanostructured Surface Using Supercritical Fluid Chemical Deposition

    Directory of Open Access Journals (Sweden)

    Mineo Hiramatsu

    2010-03-01

    Full Text Available We have developed a method of forming platinum (Pt nanoparticles using a metal organic chemical fluid deposition (MOCFD process employing a supercritical fluid (SCF, and have demonstrated the synthesis of dispersed Pt nanoparticles on the surfaces of carbon nanowalls (CNWs, two-dimensional carbon nanostructures, and carbon nanotubes (CNTs. By using SCF-MOCFD with supercritical carbon dioxide as a solvent of metal-organic compounds, highly dispersed Pt nanoparticles of 2 nm diameter were deposited on the entire surface of CNWs and CNTs. The SCF-MOCFD process proved to be effective for the synthesis of Pt nanoparticles on the entire surface of intricate carbon nanostructures with narrow interspaces.

  4. The role of oxygen in the deposition of copper–calcium thin film as diffusion barrier for copper metallization

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Zhinong, E-mail: znyu@bit.edu.cn [School of Optoelectronics and Beijing Engineering Research Center of Mixed Reality and Advanced Display, Beijing Institute of Technology, Beijing 100081 (China); Ren, Ruihuang [School of Optoelectronics and Beijing Engineering Research Center of Mixed Reality and Advanced Display, Beijing Institute of Technology, Beijing 100081 (China); Xue, Jianshe; Yao, Qi; Li, Zhengliang; Hui, Guanbao [Beijing BOE Optoelectronics Technology Co., Ltd, Beijing 100176 (China); Xue, Wei [School of Optoelectronics and Beijing Engineering Research Center of Mixed Reality and Advanced Display, Beijing Institute of Technology, Beijing 100081 (China)

    2015-02-15

    Highlights: • The CuCa film as the diffusion barrier of Cu film improves the adhesion of Cu film. • The introduction of oxygen into the deposition of CuCa film is necessary to improve the adhesion of Cu film. • The CuCa alloy barrier layer deposited at oxygen atmosphere has perfect anti-diffusion between Cu film and substrate. - Abstract: The properties of copper (Cu) metallization based on copper–calcium (CuCa) diffusion barrier as a function of oxygen flux in the CuCa film deposition were investigated in view of adhesion, diffusion and electronic properties. The CuCa film as the diffusion barrier of Cu film improves the adhesion of Cu film, however, and increases the resistance of Cu film. The introduction of oxygen into the deposition of CuCa film induces the improvement of adhesion and crystallinity of Cu film, but produces a slight increase of resistance. The increased resistance results from the partial oxidation of Cu film. The annealing process in vacuum further improves the adhesion, crystallinity and conductivity of Cu film. X-ray diffraction (XRD) and Auger electron spectroscopy (AES) show that the CuCa alloy barrier layer deposited at oxygen atmosphere has perfect anti-diffusion between Cu film and substrate due to the formation of Ca oxide in the interface of CuCa/substrate.

  5. Site-specific carbon deposition for hierarchically ordered core/shell-structured graphitic carbon with remarkable electrochemical performance.

    Science.gov (United States)

    Lv, Yingying; Wu, Zhangxiong; Qian, Xufang; Fang, Yin; Feng, Dan; Xia, Yongyao; Tu, Bo; Zhao, Dongyuan

    2013-10-01

    A fascinating core-shell-structured graphitic carbon material composed of ordered microporous core and uniform mesoporous shell is fabricated for the first time through a site-specific chemical vapor deposition process by using a nanozeolite@mesostructured silica composite molecular sieve as the template. The mesostructure-directing agent cetyltrimethylammonium bromide in the shell of the template can be either burned off or carbonized so that it is successfully utilized as a pore switch to turn the shell of the template "on" or "off" to allow selective carbon deposition. The preferred carbon deposition process can be performed only in the inner microporous zeolite cores or just within the outer mesoporous shells, resulting in a zeolite-like ordered microporous carbon or a hollow mesoporous carbon. Full carbon deposition in the template leads to the new core-shell-structured microporous@mesoporous carbon with a nanographene-constructed framework for fast electron transport, a microporous nanocore with large surface area for high-capacity storage of lithium ions, a mesoporous shell with highly opened mesopores as a transport layer for lithium ions and electron channels to access inner cores. The ordered micropores are protected by the mesoporous shell, avoiding pore blockage as the formation of solid electrolyte interphase layers. Such a unique core-shell-structured microporous@mesoporous carbon material represents a newly established lithium ion storage model, demonstrating high reversible energy storage, excellent rate capability, and long cyclic stability.

  6. Isolation and characterization of biogenic calcium carbonate/phosphate from oral bacteria and their adhesion studies on YSZ-coated titanium substrate for dental implant application

    Indian Academy of Sciences (India)

    GOBI SARAVANAN KALIARAJ; KAMALAN KIRUBAHARAN; G PRADHABAN; P KUPPUSAMI; VINITA VISHWAKARMA

    2016-04-01

    Biogenic calcium carbonate/phosphate were isolated and characterized from oral bacteria (CPOB). The crystalline nature and morphology of calcium carbonate/phosphate were characterized by X-ray diffraction (XRD)and field emission scanning electron microscopy (FESEM), respectively. XRD analysis revealed the cubic phase of YSZ coating as well as biogenic calcium carbonate (rhombohedral) and calcium phosphate oxide (hexagonal) wasobserved from CPOB. FESEM confirmed the extracellular synthesis of calcium compounds. Bacterial adhesion result reveals that YSZ coating drastically reduce bacterial invasion than titanium substrate.

  7. Electrophoretic deposition of iron catalyst on C-fiber textiles for the growth of carbon nanofibers.

    Science.gov (United States)

    Lee, Sang-Won; Lee, Chang-Seop

    2014-11-01

    In this study, carbon nanofibers synthesis has been conducted by chemical vapor deposition on C-fiber textiles coated with an iron catalyst via electrophoretic deposition. C-fiber textiles were oxidized with nitric acid before the iron catalyst was plated by electrophoretic deposition. Due to oxidation, the hydroxyl group was created on the C-fiber textiles and was used as an active site for iron catalyst deposition. It was verified that the iron catalyst was deposited on the C-fiber textiles, while current, voltage, and deposition time varied and the concentration of electrolyte was kept constant in electrophoretic deposition. After being deposited, the iron particles were dried in oven for 24 hours and reduced by hydrogen gas in a furnace. Ethylene gas was introduced for the growth of carbon nanofibers and the growth temperature was then varied to find the optimal growth temperature of the carbon nanofibers. Thus, the characteristics of carbon nanofibers were analyzed by Scanning Electron Microscopy (SEM), Energy Dispersive Spectroscopy (EDS), N2-sorption (BET), X-Ray Diffraction (XRD), and X-ray Photoelectron Spectroscopy (XPS). It is verified that the iron particles were most evenly deposited at 0.1 A for 3 minutes. Carbon nanofibers grew to 150-200 nm most evenly at 600 degrees C via temperature variations in CVD.

  8. Effect of molecular weight on the electrophoretic deposition of carbon black nanoparticles in moderately viscous systems.

    Science.gov (United States)

    Modi, Satyam; Panwar, Artee; Mead, Joey L; Barry, Carol M F

    2013-08-06

    Electrophoretic deposition from viscous media has the potential to produce in-mold assembly of nanoparticles onto three-dimensional parts in high-rate, polymer melt-based processes like injection molding. The effects of the media's molecular weight on deposition behavior were investigated using a model system of carbon black and polystyrene in tetrahydrofuran. Increases in molecular weight reduced the electrophoretic deposition of the carbon black particles due to increases in suspension viscosity and preferential adsorption of the longer polystyrene chains on the carbon black particles. At low deposition times (≤5 s), only carbon black deposited onto the electrodes, but the deposition decreased with increasing molecular weight and the resultant increases in suspension viscosity. For longer deposition times, polystyrene codeposited with the carbon black, with the amount of polystyrene increasing with molecular weight and decreasing with greater charge on the polystyrene molecules. This deposition behavior suggests that use of lower molecular polymers and control of electrical properties will permit electrophoretic deposition of nanoparticles from polymer melts for high-rate, one-step fabrication of nano-optical devices, biochemical sensors, and nanoelectronics.

  9. Nitrogen deposition: how important is it for global terrestrial carbon uptake?

    Directory of Open Access Journals (Sweden)

    G. Bala

    2013-07-01

    Full Text Available Global carbon budget studies indicate that the terrestrial ecosystems have remained a~large sink for carbon despite widespread deforestation activities. CO2-fertilization, N deposition and re-growth of mid-latitude forests are believed to be key drivers for land carbon uptake. In this study, we assess the importance of N deposition by performing idealized near-equilibrium simulations using the Community Land Model 4.0 (CLM4. In our equilibrium simulations, only 12–17% of the deposited Nitrogen is assimilated into the ecosystem and the corresponding carbon uptake can be inferred from a C : N ratio of 20:1. We calculate the sensitivity of the terrestrial biosphere for CO2-fertilization, climate warming and N deposition as changes in total ecosystem carbon for unit changes in global mean atmospheric CO2 concentration, global mean temperature and Tera grams of Nitrogen deposition per year, respectively. Based on these sensitivities, it is estimated that about 242 PgC could have been taken up by land due to the CO2 fertilization effect and an additional 175 PgC taken up as a result of the increased N deposition since the pre-industrial period. Because of climate warming, terrestrial ecosystem could have lost about 152 PgC during the same period. Therefore, since preindustrial times terrestrial carbon losses due to warming may have been approximately compensated by effects of increased N deposition, whereas the effect of CO2-fertilization is approximately indicative of the current increase in terrestrial carbon stock. Our simulations also suggest that the sensitivity of carbon storage to increased N deposition decreases beyond current levels, indicating climate warming effects on carbon storage may overwhelm N deposition effects in the future.

  10. Nitrogen deposition: how important is it for global terrestrial carbon uptake?

    Science.gov (United States)

    Bala, G.; Devaraju, N.; Chaturvedi, R. K.; Caldeira, K.; Nemani, R.

    2013-11-01

    Global carbon budget studies indicate that the terrestrial ecosystems have remained a large sink for carbon despite widespread deforestation activities. CO2 fertilization, N deposition and re-growth of mid-latitude forests are believed to be key drivers for land carbon uptake. In this study, we assess the importance of N deposition by performing idealized near-equilibrium simulations using the Community Land Model 4.0 (CLM4). In our equilibrium simulations, only 12-17% of the deposited nitrogen is assimilated into the ecosystem and the corresponding carbon uptake can be inferred from a C : N ratio of 20 : 1. We calculate the sensitivity of the terrestrial biosphere for CO2 fertilization, climate warming and N deposition as changes in total ecosystem carbon for unit changes in global mean atmospheric CO2 concentration, global mean temperature and Tera grams of nitrogen deposition per year, respectively. Based on these sensitivities, it is estimated that about 242 PgC could have been taken up by land due to the CO2 fertilization effect and an additional 175 PgC taken up as a result of the increased N deposition since the pre-industrial period. Because of climate warming, the terrestrial ecosystem could have lost about 152 PgC during the same period. Therefore, since pre-industrial times terrestrial carbon losses due to warming may have been more or less compensated by effects of increased N deposition, whereas the effect of CO2 fertilization is approximately indicative of the current increase in terrestrial carbon stock. Our simulations also suggest that the sensitivity of carbon storage to increased N deposition decreases beyond current levels, indicating that climate warming effects on carbon storage may overwhelm N deposition effects in the future.

  11. Calcium and chemical looping technology for power generation and carbon dioxide (CO2) capture solid oxygen- and CO2-carriers

    CERN Document Server

    Fennell, Paul

    2015-01-01

    Calcium and Chemical Looping Technology for Power Generation and Carbon Dioxide (CO2) Capture reviews the fundamental principles, systems, oxygen carriers, and carbon dioxide carriers relevant to chemical looping and combustion. Chapters review the market development, economics, and deployment of these systems, also providing detailed information on the variety of materials and processes that will help to shape the future of CO2 capture ready power plants. Reviews the fundamental principles, systems, oxygen carriers, and carbon dioxide carriers relevant to calcium and chemical loopingProvi

  12. Patterned deposition of multi-walled carbon nanotubes on self-assembled monolayers

    Institute of Scientific and Technical Information of China (English)

    PENG Yitian; HU Yuanzhong; WANG Hui

    2006-01-01

    Patterned chemical template consisting of both amine- and methyl-terminated self-assembled monolayers has been fabricated. The deposition of carbon nanotubes is carried out by immerging the patterned substrate into dimethylformamide (DMF) solution with suspended carbon nanotubes (CNTs). SEM images show a successful patterned deposition that carbon nanotubes selectively deposit in the area with amino-terminated SAMs due to the strong attract force between the monolayer and the suspended CNTs. This experiment provides an opportunity for manipulating individual CNTs, and represents a significant step in development of CNTs-based nanodevices.

  13. Characterization of a biodegradable coralline hydroxyapatite/calcium carbonate composite and its clinical implementation.

    Science.gov (United States)

    Fu, Kun; Xu, Qingguo; Czernuszka, Jan; Triffitt, James T; Xia, Zhidao

    2013-12-01

    A partially converted, biodegradable coralline hydroxyapatite/calcium carbonate (CHACC) composite comprising a coral calcium carbonate scaffold enveloped by a thin layer of hydroxyapatite was used in the present study. The CHACC was characterized using powder x-ray diffraction, scanning electron microscopy and energy dispersive x-ray spectroscopy. The ability of the CHACC to promote conductive osteogenesis was assessed in vitro using human mesenchymal stem cells (hMSCs) and in vivo using an immunodeficient mouse model. The clinical performance of CHACC as a bone substitute to fill voids caused by excision of bone tumours was also observed in 16 patients. The CHACC was found to consist of two overlapping layers both morphologically and chemically. Hydroxyapatite formed a thin layer of nanocrystals on the surface and a thick rough crystal layer of around 30 µm in thickness enveloping the rock-like core calcium carbonate exoskeletal architecture. hMSCs cultured on CHACC in osteogenic medium demonstrated significant osteogenic differentiation. After subcutaneous implantation of CHACC incorporating osteogenically differentiated hMSCs and an anti-resorptive agent, risedronate, into an immunodeficient mouse model, bone formation was observed on the surface of the implants. Clinical application of CHACC alone in 16 patients for bone augmentation after tumour removal showed that after implantation, visible callus formation was observed at one month and clinical bone healing achieved at four months. The majority of the implanted CHACC was degraded in 18-24 months. In conclusion, CHACC appears to be an excellent biodegradable bone graft material. It biointegrates with the host, is osteoconductive, biodegradable and can be an attractive alternative to autogenous grafts.

  14. Effect of Different Catalyst Deposition Technique on Aligned Multiwalled Carbon Nanotubes Grown by Thermal Chemical Vapor Deposition

    Directory of Open Access Journals (Sweden)

    Mohamed Shuaib Mohamed Saheed

    2014-01-01

    Full Text Available The paper reported the investigation of the substrate preparation technique involving deposition of iron catalyst by electron beam evaporation and ferrocene vaporization in order to produce vertically aligned multiwalled carbon nanotubes array needed for fabrication of tailored devices. Prior to the growth at 700°C in ethylene, silicon dioxide coated silicon substrate was prepared by depositing alumina followed by iron using two different methods as described earlier. Characterization analysis revealed that aligned multiwalled carbon nanotubes array of 107.9 µm thickness grown by thermal chemical vapor deposition technique can only be achieved for the sample with iron deposited using ferrocene vaporization. The thick layer of partially oxidized iron film can prevent the deactivation of catalyst and thus is able to sustain the growth. It also increases the rate of permeation of the hydrocarbon gas into the catalyst particles and prevents agglomeration at the growth temperature. Combination of alumina-iron layer provides an efficient growth of high density multiwalled carbon nanotubes array with the steady growth rate of 3.6 µm per minute for the first 12 minutes and dropped by half after 40 minutes. Thicker and uniform iron catalyst film obtained from ferrocene vaporization is attributed to the multidirectional deposition of particles in the gaseous form.

  15. Carbon, oxygen and boron isotopic studies of Huangbaishuwan witherite deposit at Ziyang and Wenyuhe witherite deposit at Zhushan

    Institute of Scientific and Technical Information of China (English)

    Lü; Zhicheng(吕志成); LIU; Congqiang(刘丛强); LIU; Jiajun(刘家军); ZHAO; Zhiqi(赵志琦)

    2003-01-01

    Being stratiform or stratoid, the Huangbaishuwan witherite deposit at Ziyang and the Wenyuhe witherite-barite deposit at Zhushan occur in the lower Lower Cambrian siliceous rocks and the orebodies are remarkably controlled by lithological character and petrography. Boron, carbon and oxygen isotopic studies of witherite, barytocalcite and calcite have shown that the carbon, involved in the formation of these minerals, was derived mainly from hydrocarbons and biogenetic gases resulting from degradation, polycondensation and dehydroxylation of bio-organic matter in sediments at the early stage of diagenesis; the boron was a mixture of boron in pore water and that released in the process of degradation of organic matter, with a minor amount of boron from cycling brines in the deep interior of the basin. Boron, carbon and oxygen isotopic studies unanimously demonstrated that witherite was precipitated in this sort of organic carbon-rich pore water medium during the early stage of diagenesis. Extensive occurrence of biodetritus and clastic texture in witherite ores strongly evidenced that Ba2+ was concentrated and settled down in the form of bio-barite on the seafloor as a result of biological processes, thereafter forming the initially enriched orebodies of barium deposits. Biological processes in seawater and early diagenesis in sediments are the major ore-forming mechanisms of witherite deposits in the region studied.

  16. Atomic Layer Deposition on Carbon Nanotubes and their Assemblies

    Science.gov (United States)

    Stano, Kelly Lynn

    Global issues related to energy and the environment have motivated development of advanced material solutions outside of traditional metals ceramics, and polymers. Taking inspiration from composites, where the combination of two or more materials often yields superior properties, the field of organic-inorganic hybrids has recently emerged. Carbon nanotube (CNT)-inorganic hybrids have drawn widespread and increasing interest in recent years due to their multifunctionality and potential impact across several technologically important application areas. Before the impacts of CNT-inorganic hybrids can be realized however, processing techniques must be developed for their scalable production. Optimization in chemical vapor deposition (CVD) methods for synthesis of CNTs and vertically aligned CNT arrays has created production routes both high throughput and economically feasible. Additionally, control of CVD parameters has allowed for growth of CNT arrays that are able to be drawn into aligned sheets and further processed to form a variety of aligned 1, 2, and 3-dimensional bulk assemblies including ribbons, yarns, and foams. To date, there have only been a few studies on utilizing these bulk assemblies for the production of CNT-inorganic hybrids. Wet chemical methods traditionally used for fabricating CNT-inorganic hybrids are largely incompatible with CNT assemblies, since wetting and drying the delicate structures with solvents can destroy their structure. It is therefore necessary to investigate alternative processing strategies in order to advance the field of CNT-inorganic hybrids. In this dissertation, atomic layer deposition (ALD) is evaluated as a synthetic route for the production of large-scale CNT-metal oxide hybrids as well as pure metal oxide architectures utilizing CNT arrays, ribbons, and ultralow density foams as deposition templates. Nucleation and growth behavior of alumina was evaluated as a function of CNT surface chemistry. While highly graphitic

  17. Sucrose/bovine serum albumin mediated biomimetic crystallization of calcium carbonate

    Indian Academy of Sciences (India)

    Cheng-Li Yao; Wang-Hua Xu; Ai-Min Ding; Jin-Mao Zhu

    2009-01-01

    To understand the role of the sucrose/bovine serum albumin system in the biomineralization process, we have tested the influence of different concentration of the sucrose/bovine serum albumin (BSA) on calcium carbonate (CaCO3) precipitation. The CaCO3 crystals were characterized by scanning electron microscope (SEM), Fourier transform infrared spectrograph (FT-IR) and powder X-ray diffractometry (XRD). The possible formation mechanism of CaCO3 in the sucrose/bovine serum albumin system was discussed.

  18. Radiation does response of calcium carbonate crystal in marine shells samples

    Directory of Open Access Journals (Sweden)

    Changkian, S.

    2002-01-01

    Full Text Available A study of the evolution of element, crystal structure and thermoluminescence signal versus gamma irradiation dose were carried out for calcite shells samples. The composition of element was studied by X-ray fluorescence spectrometer. As identified by X-ray diffraction and SEM/EDS analysis, two polymorphs of calcium-carbonate were extracted: calcite and aragonite. The evolution of TL signal versus gamma irradiation dose using the TL reader (Harshaw 2000 was initially dependent on crystal structure and fading effect of the thermoluminescence signal .

  19. A comparative study of calcium absorption following a single serving administration of calcium carbonate powder versus calcium citrate tablets in healthy premenopausal women

    OpenAIRE

    Wang, Haiyuan; Bua, Peter; Capodice, Jillian

    2014-01-01

    Background: Calcium is an essential mineral often taken as a daily, long-term nutritional supplement. Data suggests that once-daily dosing is important with regard to long-term compliance of both drugs and nutritional supplements.Objective: This study was undertaken to compare the bioavailability of a single serving of two calcium supplements in healthy, premenopausal women.Design: A two-period, crossover bioavailability study of a single serving of calcium citrate tablets (two tablets=500 mg...

  20. A comparative study of calcium absorption following a single serving administration of calcium carbonate powder versus calcium citrate tablets in healthy premenopausal women

    OpenAIRE

    Haiyuan Wang; Peter Bua; Jillian Capodice

    2014-01-01

    Background: Calcium is an essential mineral often taken as a daily, long-term nutritional supplement. Data suggests that once-daily dosing is important with regard to long-term compliance of both drugs and nutritional supplements. Objective: This study was undertaken to compare the bioavailability of a single serving of two calcium supplements in healthy, premenopausal women. Design: A two-period, crossover bioavailability study of a single serving of calcium citrate tablets (two tablets=500 ...

  1. A comparative study of calcium absorption following a single serving administration of calcium carbonate powder versus calcium citrate tablets in healthy premenopausal women

    OpenAIRE

    Wang, Haiyuan; Bua, Peter; Capodice, Jillian

    2014-01-01

    Background Calcium is an essential mineral often taken as a daily, long-term nutritional supplement. Data suggests that once-daily dosing is important with regard to long-term compliance of both drugs and nutritional supplements. Objective This study was undertaken to compare the bioavailability of a single serving of two calcium supplements in healthy, premenopausal women. Design A two-period, crossover bioavailability study of a single serving of calcium citrate tablets (two tablets=500 mg ...

  2. Carbon deposition in an SOFC fueled by tar-laden biomass gas: a thermodynamic analysis

    Science.gov (United States)

    Singh, Devinder; Hernández-Pacheco, Eduardo; Hutton, Phillip N.; Patel, Nikhil; Mann, Michael D.

    This work presents a thermodynamic analysis of the carbon deposition in a solid oxide fuel cell (SOFC) fueled by a biomass gasifier. Integrated biomass-SOFC units offer considerable benefits in terms of efficiency and fewer emissions. SOFC-based power plants can achieve a system efficiency of 70-80% (including heat utilization) as compared to 30-37% for conventional systems. The fuel from the biomass gasifier can contain considerable amounts of tars depending on the type of gasifier used. These tars can lead to the deposition of carbon at the anode side of SOFCs and affect the performance of the fuel cells. This paper thermodynamically studies the risk of carbon deposition due to the tars present in the feed stream and the effect various parameters like current density, steam, and temperature have on carbon deposition. Since tar is a complex mixture of aromatics, it is represented by a mixture of toluene, naphthalene, phenol, and pyrene. A total of 32 species are considered for the thermodynamic analysis, which is done by the Gibbs energy minimization technique. The carbon deposition is shown to decrease with an increase in current density and becomes zero after a critical current density. Steam in the feed stream also decreases the amount of carbon deposition. With the increase in temperature the amount of carbon first decreases and then increases.

  3. Surface treatment effect on Si (111) substrate for carbon deposition using DC unbalanced magnetron sputtering

    Energy Technology Data Exchange (ETDEWEB)

    Aji, A. S., E-mail: aji.ravazes70@gmail.com; Sahdan, M. F.; Hendra, I. B.; Dinari, P.; Darma, Y. [Quantum Semiconductor and Devices Lab., Physics of Material Electronics Research Division, Department of Physics, Institut Teknologi Bandung (Indonesia)

    2015-04-16

    In this work, we studied the effect of HF treatment in silicon (111) substrate surface for depositing thin layer carbon. We performed the deposition of carbon by using DC Unbalanced Magnetron Sputtering with carbon pallet (5% Fe) as target. From SEM characterization results it can be concluded that the carbon layer on HF treated substrate is more uniform than on substrate without treated. Carbon deposition rate is higher as confirmed by AFM results if the silicon substrate is treated by HF solution. EDAX characterization results tell that silicon (111) substrate with HF treatment have more carbon fraction than substrate without treatment. These results confirmed that HF treatment on silicon Si (111) substrates could enhance the carbon deposition by using DC sputtering. Afterward, the carbon atomic arrangement on silicon (111) surface is studied by performing thermal annealing process to 900 °C. From Raman spectroscopy results, thin film carbon is not changing until 600 °C thermal budged. But, when temperature increase to 900 °C, thin film carbon is starting to diffuse to silicon (111) substrates.

  4. Aligned carbon nanotube, graphene and graphite oxide thin films via substrate-directed rapid interfacial deposition.

    Science.gov (United States)

    D'Arcy, Julio M; Tran, Henry D; Stieg, Adam Z; Gimzewski, James K; Kaner, Richard B

    2012-05-21

    A procedure for depositing thin films of carbon nanostructures is described that overcomes the limitations typically associated with solution based methods. Transparent and conductively continuous carbon coatings can be grown on virtually any type of substrate within seconds. Interfacial surface tension gradients result in directional fluid flow and film spreading at the water/oil interface. Transparent films of carbon nanostructures are produced including aligned ropes of single-walled carbon nanotubes and assemblies of single sheets of chemically converted graphene and graphite oxide. Process scale-up, layer-by-layer deposition, and a simple method for coating non-activated hydrophobic surfaces are demonstrated.

  5. Ultrathin diamond-like carbon films deposited by filtered carbon vacuum arcs

    Energy Technology Data Exchange (ETDEWEB)

    Anders, Andre; Fong, Walton; Kulkarni, Ashok; Ryan, Francis W.; Bhatia, C. Singh

    2001-07-13

    Ultrathin (< 5 nm) hard carbon films are of great interest to the magnetic storage industry as the areal density approaches 100 Gbit/in{sup 2}. These films are used as overcoats to protect the magnetic layers on disk media and the active elements of the read-write slider. Tetrahedral amorphous carbon films can be produced by filtered cathodic arc deposition, but the films will only be accepted by the storage industry only if the ''macroparticle'' issue has been solved. Better plasma filters have been developed over recent years. Emphasis is put on the promising twist filter system - a compact, open structure that operates with pulsed arcs and high magnetic field. Based on corrosion tests it is shown that the macroparticle reduction by the twist filter is satisfactory for this demanding application, while plasma throughput is very high. Ultrathin hard carbon films have been synthesized using S-filter and twist filter systems. Film properties such as hardness, elastic modulus, wear, and corrosion resistance have been tested.

  6. Deposition of calcium phosphate coatings using condensed phosphates (P2O7(4-) and P3O10(5-)) as phosphate source through induction heating.

    Science.gov (United States)

    Zhou, Huan; Hou, Saisai; Zhang, Mingjie; Yang, Mengmeng; Deng, Linhong; Xiong, Xinbo; Ni, Xinye

    2016-12-01

    In present work condensed phosphates (P2O7(4-) and P3O10(5-)) were used as phosphate source in induction heating to deposit calcium phosphate coatings. The phase, morphology, and composition of different phosphate-related coatings were characterized and compared using XRD, FTIR, and SEM analyses. Results showed that P2O7(4-)formed calcium pyrophosphate hydrate coatings with interconnected cuboid-like particles. The as-deposited calcium tripolyphosphate hydrate coating with P3O10(5-) was mainly composed of flower-like particles assembled by plate-like crystals. The bioactivity and cytocompatibility of the coatings were also studied. Moreover, the feasibility of using hybrid phosphate sources for preparing and depositing coatings onto magnesium alloy was investigated.

  7. Experimental modelling of Calcium carbonate precipitation in the presence of phototrophic anaerobic bacteria Rhodovulum sp.

    Science.gov (United States)

    Bundeleva, Irina; Shirokova, Liudmila; Benezeth, Pascale; Pokrovsky, Oleg; Kompantseva, Elena

    2010-05-01

    -potential of the cells. To characterise the link between the rate of bacterial growth (biomass production) and the rate of CaCO3 precipitation, batch kinetic experiments were performed. These experiments were carried out in closed (anaerobic) bottles with initial concentration of calcium from 1 to 20 mM and from 5 to 20 mM bicarbonate. The biomass of cells, pH, [Ca2+] and [Alk] were measured as a function of time. Blank experiments (without cell or autoclaved cells) were always carried out. We found that the optimal conditions for both CaCO3 precipitation and biomass increase for the culture Rhodovulum sp. A-20s, is calcium concentration of 3 mM, whatever the concentration of bicarbonate (5, 10, 15 mM). Note also that for calcium concentration higher than 3 mM, the biomass production decreases. In the case of strictly anaerobic Rhodovulum sp. S-1765 bacteria, the optimal conditions for calcium carbonate precipitation is observed for the bicarbonate concentration of 10 mM, whatever the calcium concentration (3, 5, 10 mM). Overall, the present study allows quantitative modeling of bacterially-induced CaCO3 precipitation. It helps to distinguish between the effect of cell surface functional groups, surface electrical charge, soluble organic matter and metabolic change of solution pH on the rate and nature of precipitating calcium carbonate solid phase.

  8. A laboratory study of the heterogeneous reaction of nitric acid on calcium carbonate particles

    Science.gov (United States)

    Goodman, A. L.; Underwood, G. M.; Grassian, V. H.

    2000-12-01

    It has been postulated that the reaction of nitric acid with calcium carbonate, namely, CaCO3(s) + 2HNO3(g) → Ca(NO3)2(s) + CO2(g) + H2O(g), plays an important role in the atmosphere. In this study, transmission FTIR spectroscopy, diffuse reflectance UV-visible spectroscopy, transmission electron microscopy and a Knudsen cell reactor coupled to a quadrupole mass spectrometer have been used to investigate the heterogeneous reactivity of HNO3 on CaCO3 at 295 K as a function of relative humidity. Transmission FTIR spectroscopy was used to probe both gas-phase and adsorbed products and showed that the reaction of HNO3 and CaCO3 is limited to the surface of the CaCO3 particle in the absence of adsorbed water. However, in the presence of water vapor, the reaction is greatly enhanced and is not limited to the surface of the particle producing both solid calcium nitrate and gaseous carbon dioxide. The enhanced reactivity of the particles is attributed to the presence of a layer of adsorbed water on the particle surface. The amount of adsorbed water on the particle surface is strongly dependent on the extent of the reaction. This can be understood in terms of the increased hydrophilicity of calcium nitrate as compared to calcium carbonate. Data from experiments using a mass-calibrated Knudsen cell reactor showed the stoichiometry for the reaction determined from gas-phase species deviated from that expected from the balanced equation. Water adsorption on the particle surface and gases dissolved into the water layer appear to be the cause of this discrepancy. The measured uptake coefficient accounting for the BET area of the sample is determined to be 2.5±0.1×10-4 for HNO3 on CaCO3 under dry conditions and is found to increase in the presence of water vapor. Atmospheric implications of the results presented here are discussed.

  9. Biocalcite, a multifunctional inorganic polymer: Building block for calcareous sponge spicules and bioseed for the synthesis of calcium phosphate-based bone

    Directory of Open Access Journals (Sweden)

    Xiaohong Wang

    2014-05-01

    Full Text Available Calcium carbonate is the material that builds up the spicules of the calcareous sponges. Recent results revealed that the calcium carbonate/biocalcite-based spicular skeleton of these animals is formed through an enzymatic mechanism, such as the skeleton of the siliceous sponges, evolutionarily the oldest animals that consist of biosilica. The enzyme that mediates the calcium carbonate deposition has been identified as a carbonic anhydrase (CA and has been cloned from the calcareous sponge species Sycon raphanus. Calcium carbonate deposits are also found in vertebrate bones besides the main constituent, calcium phosphate/hydroxyapatite (HA. Evidence has been presented that during the initial phase of HA synthesis poorly crystalline carbonated apatite is deposited. Recent data summarized here indicate that during early bone formation calcium carbonate deposits enzymatically formed by CA, act as potential bioseeds for the precipitation of calcium phosphate mineral onto bone-forming osteoblasts. Two different calcium carbonate phases have been found during CA-driven enzymatic calcium carbonate deposition in in vitro assays: calcite crystals and round-shaped vaterite deposits. The CA provides a new target of potential anabolic agents for treatment of bone diseases; a first CA activator stimulating the CA-driven calcium carbonate deposition has been identified. In addition, the CA-driven calcium carbonate crystal formation can be frozen at the vaterite state in the presence of silintaphin-2, an aspartic acid/glutamic acid-rich sponge-specific protein. The discovery that calcium carbonate crystals act as bioseeds in human bone formation may allow the development of novel biomimetic scaffolds for bone tissue engineering. Na-alginate hydrogels, enriched with biosilica, have recently been demonstrated as a suitable matrix to embed bone forming cells for rapid prototyping bioprinting/3D cell printing applications.

  10. Nanostructured silicon carbon thin films grown by plasma enhanced chemical vapour deposition technique

    Energy Technology Data Exchange (ETDEWEB)

    Coscia, U. [Dipartimento di Fisica, Università di Napoli “Federico II” Complesso Universitario MSA, via Cinthia, 80126 Napoli (Italy); CNISM Unita' di Napoli, Complesso Universitario MSA, via Cinthia, 80126 Napoli (Italy); Ambrosone, G., E-mail: ambrosone@na.infn.it [Dipartimento di Fisica, Università di Napoli “Federico II” Complesso Universitario MSA, via Cinthia, 80126 Napoli (Italy); SPIN-CNR, Complesso Universitario MSA, via Cinthia, 80126 Napoli (Italy); Basa, D.K. [Department of Physics, Utkal University, Bhubaneswar 751004 (India); Rigato, V. [INFN Laboratori Nazionali Legnaro, 35020 Legnaro (Padova) (Italy); Ferrero, S.; Virga, A. [Dipartimento di Scienza Applicata e Tecnologia, Politecnico di Torino, C.so Duca degli Abruzzi 24, 10129 Torino (Italy)

    2013-09-30

    Nanostructured silicon carbon thin films, composed of Si nanocrystallites embedded in hydrogenated amorphous silicon carbon matrix, have been prepared by varying rf power in ultra high vacuum plasma enhanced chemical vapour deposition system using silane and methane gas mixtures diluted in hydrogen. In this paper we have studied the compositional, structural and electrical properties of these films as a function of rf power. It is shown that with increasing rf power the atomic densities of carbon and hydrogen increase while the atomic density of silicon decreases, resulting in a reduction in the mass density. Further, it is demonstrated that carbon is incorporated into amorphous matrix and it is mainly bonded to silicon. The study has also revealed that the crystalline volume fraction decreases with increase in rf power and that the films deposited with low rf power have a size distribution of large and small crystallites while the films deposited with relatively high power have only small crystallites. Finally, the enhanced transport properties of the nanostructured silicon carbon films, as compared to amorphous counterpart, have been attributed to the presence of Si nanocrystallites. - Highlights: • The mass density of silicon carbon films decreases from 2.3 to 2 g/cm{sup 3}. • Carbon is incorporated in the amorphous phase and it is mainly bonded to silicon. • Nanostructured silicon carbon films are deposited at rf power > 40 W. • Si nanocrystallites in amorphous silicon carbon enhance the electrical properties.

  11. Transformation of amorphous calcium carbonate to rod-like single crystal calcite via "copying" collagen template.

    Science.gov (United States)

    Xue, Zhonghui; Hu, Binbin; Dai, Shuxi; Du, Zuliang

    2015-10-01

    Collagen Langmuir films were prepared by spreading the solution of collagen over deionized water, CaCl2 solution and Ca(HCO3)2 solution. Resultant collagen Langmuir monolayers were then compressed to a lateral pressure of 10 mN/m and held there for different duration, allowing the crystallization of CaCO3. The effect of crystallization time on the phase composition and microstructure of CaCO3 was investigated. It was found that amorphous calcium carbonate (ACC) was obtained at a crystallization time of 6 h. The amorphous CaCO3 was transformed to rod-like single crystal calcite crystals at an extended crystallization time of 12 h and 24 h, via "copying" the symmetry and dimensionalities of collagen fibers. Resultant calcite crystallites were well oriented along the longitudinal axis of collagen fibers. The ordered surface structure of collagen fibers and electrostatic interactions played key roles in tuning the oriented nucleation and growth of the calcite crystallites. The mineralized collagen possessing both desired mechanical properties of collagen fiber and good biocompatibility of calcium carbonate may be assembled into an ideal biomaterial for bone implants.

  12. Application of Box-Behnken design to prepare gentamicin-loaded calcium carbonate nanoparticles.

    Science.gov (United States)

    Maleki Dizaj, Solmaz; Lotfipour, Farzaneh; Barzegar-Jalali, Mohammad; Zarrintan, Mohammad-Hossein; Adibkia, Khosro

    2016-09-01

    The aim of this research was to prepare and optimize calcium carbonate (CaCO3) nanoparticles as carriers for gentamicin sulfate. A chemical precipitation method was used to prepare the gentamicin sulfate-loaded CaCO3 nanoparticles. A 3-factor, 3-level Box-Behnken design was used for the optimization procedure, with the molar ratio of CaCl2: Na2CO3 (X1), the concentration of drug (X2), and the speed of homogenization (X3) as the independent variables. The particle size and entrapment efficiency were considered as response variables. Mathematical equations and response surface plots were used, along with the counter plots, to relate the dependent and independent variables. The results indicated that the speed of homogenization was the main variable contributing to particle size and entrapment efficiency. The combined effect of all three independent variables was also evaluated. Using the response optimization design, the optimized Xl-X3 levels were predicted. An optimized formulation was then prepared according to these levels, resulting in a particle size of 80.23 nm and an entrapment efficiency of 30.80%. It was concluded that the chemical precipitation technique, together with the Box-Behnken experimental design methodology, could be successfully used to optimize the formulation of drug-incorporated calcium carbonate nanoparticles.

  13. Study on the thermal decomposition kinetics of nano-sized calcium carbonate

    Institute of Scientific and Technical Information of China (English)

    李代禧; 史鸿运; 邓洁; 徐元植

    2003-01-01

    This study of the thermal decomposition kinetics of various average diameter nano-particles of calcium carbonate by means of TG-DTA(thermogravimetry and differential thermal analysis) showed that the thermal decomposition kinetic mechanisms of the same crystal type of calcium carbonate samples do not vary with decreasing of their average diameters; their pseudo-active energy Ea; and that the top-temperature of decomposition Tp decreases gently in the scope of micron-sized diameter, but decreases sharply when the average diameter decreases from micron region to nanometer region. The extraordinary properties of nano-particles were explored by comparing the varying regularity of the mechanisms and kinetic parameters of the solid-phase reactions as well as their structural characterization with the variation of average diameters of particles. These show that the aggregation, surface effect as well as internal aberrance and stress of the nano-particles are the main reason causing both Ea and Tp to decline sharply with the decrease of the average diameter of nano-particles.

  14. Hall Measurements on Carbon Nanotube Paper Modified With Electroless Deposited Platinum

    Directory of Open Access Journals (Sweden)

    Iwuoha Emmanuel

    2009-01-01

    Full Text Available Abstract Carbon nanotube paper, sometimes referred to as bucky paper, is a random arrangement of carbon nanotubes meshed into a single robust structure, which can be manipulated with relative ease. Multi-walled carbon nanotubes were used to make the nanotube paper, and were subsequently modified with platinum using an electroless deposition method based on substrate enhanced electroless deposition. This involves the use of a sacrificial metal substrate that undergoes electro-dissolution while the platinum metal deposits out of solution onto the nanotube paper via a galvanic displacement reaction. The samples were characterized using SEM/EDS, and Hall-effect measurements. The SEM/EDS analysis clearly revealed deposits of platinum (Pt distributed over the nanotube paper surface, and the qualitative elemental analysis revealed co-deposition of other elements from the metal substrates used. When stainless steel was used as sacrificial metal a large degree of Pt contamination with various other metals was observed. Whereas when pure sacrificial metals were used bimetallic Pt clusters resulted. The co-deposition of a bimetallic system upon carbon nanotubes was a function of the metal type and the time of exposure. Hall-effect measurements revealed some interesting fluctuations in sheet carrier density and the dominant carrier switched from N- to P-type when Pt was deposited onto the nanotube paper. Perspectives on the use of the nanotube paper as a replacement to traditional carbon cloth in water electrolysis systems are also discussed.

  15. Hall measurements on carbon nanotube paper modified with electroless deposited platinum.

    Science.gov (United States)

    Petrik, Leslie; Ndungu, Patrick; Iwuoha, Emmanuel

    2009-09-18

    Carbon nanotube paper, sometimes referred to as bucky paper, is a random arrangement of carbon nanotubes meshed into a single robust structure, which can be manipulated with relative ease. Multi-walled carbon nanotubes were used to make the nanotube paper, and were subsequently modified with platinum using an electroless deposition method based on substrate enhanced electroless deposition. This involves the use of a sacrificial metal substrate that undergoes electro-dissolution while the platinum metal deposits out of solution onto the nanotube paper via a galvanic displacement reaction. The samples were characterized using SEM/EDS, and Hall-effect measurements. The SEM/EDS analysis clearly revealed deposits of platinum (Pt) distributed over the nanotube paper surface, and the qualitative elemental analysis revealed co-deposition of other elements from the metal substrates used. When stainless steel was used as sacrificial metal a large degree of Pt contamination with various other metals was observed. Whereas when pure sacrificial metals were used bimetallic Pt clusters resulted. The co-deposition of a bimetallic system upon carbon nanotubes was a function of the metal type and the time of exposure. Hall-effect measurements revealed some interesting fluctuations in sheet carrier density and the dominant carrier switched from N- to P-type when Pt was deposited onto the nanotube paper. Perspectives on the use of the nanotube paper as a replacement to traditional carbon cloth in water electrolysis systems are also discussed.

  16. The evolution of metazoan α-carbonic anhydrases and their roles in calcium carbonate biomineralization

    OpenAIRE

    Le Roy, Nathalie; Jackson, Daniel J.; Marie, Benjamin; Ramos-Silva, Paula; Marin, Frédéric

    2014-01-01

    The carbonic anhydrase (CA; EC 4.2.1.1) superfamily is a class of ubiquitous metallo-enzymes that catalyse the reversible hydration of carbon dioxide. The ?-CA family, present in all metazoan clades, is a key enzyme involved in a wide range of physiological functions including pH regulation, respiration, photosynthesis, and biocalcification. This paper reviews the evolution of the ?-CA family, with an emphasis on metazoan ?-CA members involved in biocalcification. Phylogenetic analyses reveal...

  17. Assessing potential diagenetic alteration of primary iodine-to-calcium ratios in carbonate rocks

    Science.gov (United States)

    Hardisty, D. S.; Lu, Z.; Swart, P. K.; Planavsky, N.; Gill, B. C.; Loyd, S. J.; Lyons, T. W.

    2015-12-01

    We have evaluated iodine-to-calcium (I/Ca) ratios from a series of carbonate samples with well-constrained histories of diagenetic alteration to assess the likelihood of overprints on primary water column-derived signals. Because only the oxidized iodine species, iodate, is incorporated during carbonate precipitation, I/Ca ratios have strong potential as proxies for both marine redox and carbon cycling. This utility lies with the combination of iodate's redox sensitivity as well as the close association between iodine and marine organic matter. However, despite the possibility of large pore water iodine enrichments relative to overlying seawater, carbonate alteration under reducing diagenetic conditions, and iodate-to-iodide reduction, no study has assessed the prospect of diagenetic alteration of primary I/Ca ratios. Here, we evaluated aragonite-to-calcite transformations and dolomitization within the Key Largo Limestone of South Florida and the Clino and Unda drill cores of the Bahamas Bank. Also, early burial diagenesis was studied through analysis of I/Ca ratios in short cores from a variety of shallow settings within the Exuma Bay, Bahamas. Further, we evaluated authigenic carbonates through analysis of iodine in concretions constrained to have formed during varying stages of evolving pore fluid chemistry. In all cases, I/Ca ratios show the potential for diagenetic iodine loss relative to water-column derived values, consistent with observations of quantitative reduction of dissolved iodate to iodide in pore waters before or synchronous with carbonate alteration. In no case, however, did we observe an increase in I/Ca during diagenetic transformation. Our results suggest both that primary I/Ca values and trends can be preserved but that maximum I/Ca ratios should be considered a minimum estimate of seawater iodate. We recommend that ancient carbonates with distinct I/Ca trends not indicative of diagenetic iodine loss reflect preservation of or very early

  18. Effect of nickel introduced by electroplating on pyrocarbon deposition of carbon-fiber preforms

    Institute of Scientific and Technical Information of China (English)

    Ren Yancai; Shi Xiaohong; Li Hejun; Li Kezhi; Zhang Xin

    2014-01-01

    In order to improve the deposition rate and microstructure of pyrocarbon, nickel was introduced by electroplating on carbon fibers and used as a catalyst during the deposition of pyro-carbon at 1000 ?C using methane as a precursor gas. The distribution of nickel catalyst and the microstructure of pyrocarbon were characterized by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), and Raman micro-spectrometry. Results show that nano-sized nickel particles could be well distributed on carbon fibers and the pyrocarbon deposited catalytically had a smaller d002 value and a higher graphitization degree compared with that without catalyst. In addition, the deposition rate of pyrocarbon in each hour was measured. The deposition rate of pyrocarbon in the first hour was more than 10 times when carbon cloth substrates were doped with nickel catalysts as compared to the pure carbon cloths. The pyrocarbon gained by rapid deposition may include two parts, which are generation directly on the nickel catalyst and formation with the carbon nanofibers as crystal nucleus.

  19. Restoration of parathyroid function after change of phosphate binder from calcium carbonate to lanthanum carbonate in hemodialysis patients with suppressed serum parathyroid hormone.

    Science.gov (United States)

    Inaba, Masaaki; Okuno, Senji; Nagayama, Harumi; Yamada, Shinsuke; Ishimura, Eiji; Imanishi, Yasuo; Shoji, Shigeichi

    2015-03-01

    Control of phosphate is the most critical in the treatment of chronic kidney disease with mineral and bone disorder (CKD-MBD). Because calcium-containing phosphate binder to CKD patients is known to induce adynamic bone disease with ectopic calcification by increasing calcium load, we examined the effect of lanthanum carbonate (LaC), a non-calcium containing phosphate binder, to restore bone turnover in 27 hemodialysis patients with suppressed parathyroid function (serum intact parathyroid hormone [iPTH] ≦ 150 pg/mL). At the initiation of LaC administration, the dose of calcium-containing phosphate binder calcium carbonate (CaC) was withdrawn or reduced based on serum phosphate. After initiation of LaC administration, serum calcium and phosphate decreased significantly by 4 weeks, whereas whole PTH and iPTH increased. A significant and positive correlation between decreases of serum calcium, but not phosphate, with increases of whole PTH and iPTH, suggested that the decline in serum calcium with reduction of calcium load by LaC might increase parathyroid function. Serum bone resorption markers, such as serum tartrate-resistant acid phosphatase 5b, and N-telopeptide of type I collagen increased significantly by 4 weeks after LaC administration, which was followed by increases of serum bone formation markers including serum bone alkaline phosphatase, intact procollagen N-propeptide, and osteocalcin. Therefore, it was suggested that LaC attenuated CaC-induced suppression of parathyroid function and bone turnover by decreasing calcium load. In conclusion, replacement of CaC with LaC, either partially or totally, could increase parathyroid function and resultant bone turnover in hemodialysis patients with serum iPTH ≦ 150 pg/mL.

  20. Deposition and characterization of hydrogenated diamond-like carbon thin films on rubber seals

    NARCIS (Netherlands)

    Pei, Y.T.; Bui, X.L.; Hosson, J.Th.M. De

    2010-01-01

    Thin films of hydrogenated diamond-like carbon (DLC) have been deposited on hydrogenated nitrile butadiene rubber (HNBR) for reduction of friction and enhancement of wear resistance of dynamic rubber seals. The wax removal and pre-deposition plasma treatment of HNBR substrates are proven to be cruci

  1. Soil aggregation and the stabilization of organic carbon as affected by erosion and deposition

    NARCIS (Netherlands)

    Wang, X.; Cammeraat, E.L.H.; Cerli, C.; Kalbitz, K.

    2014-01-01

    The importance of soil aggregation in determining the dynamics of soil organic carbon (SOC) during erosion, transportation and deposition is poorly understood. Particularly, we do not know how aggregation contributes to the often-observed accumulation of SOC at depositional sites. Our objective was

  2. Tuning calcium carbonate growth through physical confinement and templating with amyloid-like polypeptide aggregates

    Science.gov (United States)

    Colaco, Martin Francis

    The creation of useful composite materials requires precise control of the interface between the components in order to tune the overall shape and material properties. Despite the current research into nanotechnology, our ability to create materials with nanoscale precision is nascent. However, nature has a paradigm for the creation of finely structured composites under mild conditions called biomineralization. Through control of protein template assembly, solution conditions, and physical confinement, organisms are able to create useful optical and structural materials, such as bones, teeth, and mollusk shells. The objective of this thesis is to elucidate the importance of these various controls in synthetic systems to further our ability to create nanostructured materials. We begin by examining the formation of self-assembled monolayers (SAMs) of organosilanes on silica oxides. The formation of functionalized surfaces can help control the mineralization of amorphous or crystalline calcium carbonate. Long-chained organosilanes organize on surfaces to form dense, solid-like films, with the terminal groups determining the hydrophobicity and stereochemistry of the film. Our work has shown that uniform hydrophobic and hydrophilic films can be formed by using cleaned silica over glass or mica and through a vapor phase reaction over a liquid one. Additionally, we showed that mixed SAMs with phase-separated domains could be created through the selection of organosilanes and reaction conditions. We have built on these functionalized surfaces through the use of microfabrication and a gas permeable polymer to create three-dimensionally confined microcrystallizers. Other researchers have shown that one-dimensional confinement with a multi-functional surface (patterned with a small nucleating ordered region in a disordered SAM) can stabilize the creation of an amorphous calcium carbonate film before a single, large, micropatterned crystal is grown. Our work has determined

  3. The preparation and performance of calcium carbide-derived carbon/polyaniline composite electrode material for supercapacitors

    Science.gov (United States)

    Zheng, Liping; Wang, Ying; Wang, Xianyou; Li, Na; An, Hongfang; Chen, Huajie; Guo, Jia

    Calcium carbide (CaC 2)-derived carbon (CCDC)/polyaniline (PANI) composite materials are prepared by in situ chemical oxidation polymerization of an aniline solution containing well-dispersed CCDC. The structure and morphology of CCDC/PANI composite are characterized by Fourier infrared spectroscopy (FTIR), scanning electron microscope (SEM), transmission electron microscopy (TEM) and N 2 sorption isotherms. It has been found that PANI was uniformly deposited on the surface and the inner pores of CCDC. The supercapacitive behaviors of the CCDC/PANI composite materials are investigated with cyclic voltammetry (CV), galvanostatic charge/discharge and cycle life measurements. The results show that the CCDC/PANI composite electrodes have higher specific capacitances than the as grown CCDC electrodes and higher stability than the conducting polymers. The capacitance of CCDC/PANI composite electrode is as high as 713.4 F g -1 measured by cyclic voltammetry at 1 mV s -1. Besides, the capacitance retention of coin supercapacitor remained 80.1% after 1000 cycles.

  4. The preparation and performance of calcium carbide-derived carbon/polyaniline composite electrode material for supercapacitors

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Liping; Wang, Xianyou; Li, Na; An, Hongfang; Chen, Huajie [School of Chemistry, Key Laboratory of Environmentally Friendly Chemistry and Applications of Minister of Education, Xiangtan University, Hunan 411105 (China); Wang, Ying; Guo, Jia [School of Chemical Engineering and Pharmacy, Wuhan Institute of Technology, Hubei 430073 (China)

    2010-03-15

    Calcium carbide (CaC{sub 2})-derived carbon (CCDC)/polyaniline (PANI) composite materials are prepared by in situ chemical oxidation polymerization of an aniline solution containing well-dispersed CCDC. The structure and morphology of CCDC/PANI composite are characterized by Fourier infrared spectroscopy (FTIR), scanning electron microscope (SEM), transmission electron microscopy (TEM) and N{sub 2} sorption isotherms. It has been found that PANI was uniformly deposited on the surface and the inner pores of CCDC. The supercapacitive behaviors of the CCDC/PANI composite materials are investigated with cyclic voltammetry (CV), galvanostatic charge/discharge and cycle life measurements. The results show that the CCDC/PANI composite electrodes have higher specific capacitances than the as grown CCDC electrodes and higher stability than the conducting polymers. The capacitance of CCDC/PANI composite electrode is as high as 713.4 F g{sup -1} measured by cyclic voltammetry at 1 mV s{sup -1}. Besides, the capacitance retention of coin supercapacitor remained 80.1% after 1000 cycles. (author)

  5. Development and characterization of a novel bioresorbable and bioactive biomaterial based on polyvinyl acetate, calcium carbonate and coralline hydroxyapatite

    Directory of Open Access Journals (Sweden)

    Javier Aragón

    2011-03-01

    Full Text Available Coralina® HAP-200 (coralline hydroxyapatite obtained by hydrothermal treatment of marine corals and POVIAC® (polymeric matrix based on PVAc, commercial trade marks were mixed with a natural product from the Cuban sea costs, i.e. calcium carbonate from Porites Porites coral, to obtain a novel bioactive composite with potential use as bone restoration material. The samples were characterized by physical-chemical (FTIR, XRD, SEM, EDS and mechanical studies. It was shown that there is no chemical interaction between the inorganic filler and the polymer matrix, each conserving the original properties of the raw materials. The studied formulation had a compressive strength similar to that reported for trabecular bone. Scanning electron microscopy examination revealed that the addition of CaCO3 induces a change on the morphologic structure of the composite obtained after 30 days of SBF immersion. These composites generate novel biomaterials capable of promoting the deposition of a new phase, a Ca-P layer due to the bioactivity of a Ca2+ precursors.

  6. Acrylic acid-allylpolyethoxy carboxylate copolymer dispersant for calcium carbonate and iron(III) hydroxide scales in cooling water systems

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Guangqing; Huang, Jingyi; Zhou, Yuming; Yao, Qingzhao; Ling, Lei; Zhang, Peixin; Fu, Change [Southeast Univ., Nanjing (China). School of Chemistry and Chemical Engineering; Wu, Wendao; Sun, Wei; Hu, Zhengjun [Jianghai Chemical Co., Ltd., Changzhou (China)

    2012-05-15

    A novel environmentally friendly type of calcium carbonate and iron(III) scale inhibitor (ALn) was synthesized. The anti-scale property of the Acrylic acid-allylpolyethoxy carboxylate copolymer (AA-APELn or ALn) towards CaCO{sub 3} and iron(III) in the artificial cooling water was studied through static scale inhibition tests. The observation shows that both calcium carbonate and iron(III) inhibition increase with increasing the degree of polymerization of ALn from 5 to 15, and the dosage of ALn plays an important role on calcium carbonate and iron(III)-inhibition. The effect on formation of CaCO{sub 3} was investigated with a combination of scanning electronic microscopy (SEM), Transmission electron microscopy (TEM), X-ray powder diffraction (XRD) analysis and Fourier transform infrared spectrometer, respectively. The results showed that the ALn copolymer not only influences calcium carbonate crystal morphology and crystal size but also the crystallinity. The crystallization of CaCO{sub 3} in the absence of inhibitor was rhombohedral calcite crystal, whereas a mixture of calcite with vaterite crystals was found in the presence of the ALn copolymer. Inhibition mechanism is proposed that the interactions between calcium or iron ions and polyethylene glycol (PEG) are the fundamental impetus to restrain the formation of the scale in cooling water systems. (orig.)

  7. Deuterium Retention in the Co-Deposition Carbon Layers Deposited by Radio-Frequency Magnetron Sputtering in D2 Atmosphere

    Science.gov (United States)

    Zhang, Wei-Yuan; Shi, Li-Qun; Zhang, Bin; Hu, Jian-Sheng

    2014-05-01

    Carbon is deposited on C and Si substrates by rf magnetron plasma sputtering in a D2 atmosphere. The deposited layers are examined with ion beam analysis and thermal desorption spectroscopy (TDS). The growth rates of the layers deposited on Si decrease with increasing substrate temperature, while increase significantly with the increase of D2 pressure. Meanwhile, the deuterium concentrations in the layers deposited on the Si substrates decrease from 30% to 2% and from 31% to 1% on the C substrates, respectively, when the substrate temperature varies from 350K to 900 K. Similarly, the D concentration in the layer on the Si substrates increases from 3.4% to 47%, and from 8% to 35% on the C substrates when the D2 pressure increases from 0.3Pa to 8.0Pa. D desorption characterized by TDS is mainly in the forms of D2, HD, HDO, CD4, and C2D4, and a similar release peak occurs at 645 K. The release peak of D2 molecules at 960K can be attributed to the escaped gas from the thin co-deposited deuterium-rich carbon layer in the form of C-D bonding.

  8. Interlaminar improvement of carbon fiber/epoxy composites via depositing mixture of carbon nanotubes and sizing agent

    Energy Technology Data Exchange (ETDEWEB)

    Fang, Cuiqin [Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology, Beijing 100029 (China); Wang, Julin, E-mail: julinwang@126.com [Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology, Beijing 100029 (China); Zhang, Tao [Beijing Institute of Ancient Architecture, Beijing 100050 (China)

    2014-12-01

    Graphical abstract: - Highlights: • COOH-CNTs can react with sizing agent, and the optimum reaction ratio was 1:20. • Carbon fibers were dipped into the mixture bath of CNTs and sizing agent. • SEM results indicate that fibers surfaces were coated with CNTs and sizing agent. • ILSS was increased by 67.01% for the composites after the mixture coating process. • Single fibers tensile strength was maintained after the deposited process. - Abstract: The effects of deposition to carbon fibers surfaces with mixture of functionalized multi-walled carbon fibers (MWCNTs) and sizing agent were investigated. Relationships between CNTs and sizing agent were studied with Fourier transform infrared spectrometer (FTIR), X-ray photoelectron spectroscopy (XPS) and Ubbelohde viscometer. The results revealed that CNTs could react with sizing agent at 120 °C, and optimal reaction occurs when mass ratio was about 1:20. Then, carbon fibers were immersed in mixed aqueous suspension of CNTs and sizing agent with the above ratio dispersed by ultrasonication. According to scanning electron microscope (SEM) observations, fibers surfaces were coated with CNTs and sizing agent. The static contact angle tests indicated wetting performance between fibers and epoxy resin were improved after deposited procedures. Interlaminar shear strength was increased by 67.01% for fibers/epoxy resin composites after mixture deposited process. Moreover, the tensile strength of single fibers after depositing showed a slightly increase compared with that of fibers without depositing layer.

  9. Electrochemical impedance spectroscopy on nanostructured carbon electrodes grown by supersonic cluster beam deposition

    Energy Technology Data Exchange (ETDEWEB)

    Bettini, Luca Giacomo; Bardizza, Giorgio; Podesta, Alessandro; Milani, Paolo; Piseri, Paolo, E-mail: piseri@mi.infn.it [Universita degli Studi di Milano, Dipartimento di Fisica and CIMaINa (Italy)

    2013-02-15

    Nanostructured porous films of carbon with density of about 0.5 g/cm{sup 3} and 200 nm thickness were deposited at room temperature by supersonic cluster beam deposition (SCBD) from carbon clusters formed in the gas phase. Carbon film surface topography, determined by atomic force microscopy, reveals a surface roughness of 16 nm and a granular morphology arising from the low kinetic energy ballistic deposition regime. The material is characterized by a highly disordered carbon structure with predominant sp2 hybridization as evidenced by Raman spectroscopy. The interface properties of nanostructured carbon electrodes were investigated by cyclic voltammetry and electrochemical impedance spectroscopy employing KOH 1 M solution as aqueous electrolyte. An increase of the double layer capacitance is observed when the electrodes are heat treated in air or when a nanostructured nickel layer deposited by SCBD on top of a sputter deposited film of the same metal is employed as a current collector instead of a plain metallic film. This enhancement is consistent with an improved charge injection in the active material and is ascribed to the modification of the electrical contact at the interface between the carbon and the metal current collector. Specific capacitance values up to 120 F/g have been measured for the electrodes with nanostructured metal/carbon interface.

  10. The role of oxygen in the deposition of copper-calcium thin film as diffusion barrier for copper metallization

    Science.gov (United States)

    Yu, Zhinong; Ren, Ruihuang; Xue, Jianshe; Yao, Qi; Li, Zhengliang; Hui, Guanbao; Xue, Wei

    2015-02-01

    The properties of copper (Cu) metallization based on copper-calcium (CuCa) diffusion barrier as a function of oxygen flux in the CuCa film deposition were investigated in view of adhesion, diffusion and electronic properties. The CuCa film as the diffusion barrier of Cu film improves the adhesion of Cu film, however, and increases the resistance of Cu film. The introduction of oxygen into the deposition of CuCa film induces the improvement of adhesion and crystallinity of Cu film, but produces a slight increase of resistance. The increased resistance results from the partial oxidation of Cu film. The annealing process in vacuum further improves the adhesion, crystallinity and conductivity of Cu film. X-ray diffraction (XRD) and Auger electron spectroscopy (AES) show that the CuCa alloy barrier layer deposited at oxygen atmosphere has perfect anti-diffusion between Cu film and substrate due to the formation of Ca oxide in the interface of CuCa/substrate.

  11. Evidence for the involvement of carbonic anhydrase and urease in calcium carbonate formation in the gravity-sensing organ of Aplysia californica

    Science.gov (United States)

    Pedrozo, H. A.; Schwartz, Z.; Dean, D. D.; Harrison, J. L.; Campbell, J. W.; Wiederhold, M. L.; Boyan, B. D.

    1997-01-01

    To better understand the mechanisms that could modulate the formation of otoconia, calcium carbonate granules in the inner ear of vertebrate species, we examined statoconia formation in the gravity-sensing organ, the statocyst, of the gastropod mollusk Aplysia californica using an in vitro organ culture model. We determined the type of calcium carbonate present in the statoconia and investigated the role of carbonic anhydrase (CA) and urease in regulating statocyst pH as well as the role of protein synthesis and urease in statoconia production and homeostasis in vitro. The type of mineral present in statoconia was found to be aragonitic calcium carbonate. When the CA inhibitor, acetazolamide (AZ), was added to cultures of statocysts, the pH initially (30 min) increased and then decreased. The urease inhibitor, acetohydroxamic acid (AHA), decreased statocyst pH. Simultaneous addition of AZ and AHA caused a decrease in pH. Inhibition of urease activity also reduced total statoconia number, but had no effect on statoconia volume. Inhibition of protein synthesis reduced statoconia production and increased statoconia volume. In a previous study, inhibition of CA was shown to decrease statoconia production. Taken together, these data show that urease and CA play a role in regulating statocyst pH and the formation and maintenance of statoconia. CA produces carbonate ion for calcium carbonate formation and urease neutralizes the acid formed due to CA action, by production of ammonia.

  12. Removal of oxyanions from synthetic wastewater via carbonation process of calcium hydroxide: applied and fundamental aspects.

    Science.gov (United States)

    Montes-Hernandez, G; Concha-Lozano, N; Renard, F; Quirico, E

    2009-07-30

    Removal of oxyanions (selenite, selenate, arsenate, phosphate and nitrate) during calcite formation was experimentally studied using aqueous carbonation of calcium hydroxide under moderate pressure (P(CO2) congruent with 20 bar) and temperature (30 degrees C). The effects of Ca(OH)(2) dose (10 and 20 g), Ca(OH)(2) source (commercial pure material or alkaline paper mill waste) and oxyanion initial concentration (from 0 to 70 mg atom/L) were investigated for this anisobaric gas-liquid-solid system. The Ca(OH)(2) carbonation reaction allowed successfully the removal of selenite (>90%), arsenate (>78%) and phosphate (congruent with 100%) from synthetic solutions. Conversely, nitrate and selenate had not any physicochemical affinity/effect during calcite formation. The rate of CO(2) transfer during calcite formation in presence of oxyanions was equal or slower than for an oxyanion-free system, allowing to define a retarding kinetic factor RF that can vary between 0 (no retarding effect) to 1 (total inhibition). For selenite and phosphate RF was quite high, close to 0.3. A small retarding effect was detected for arsenate (RF approximately 0.05) and no retarding effect was detected for selenate and nitrate (RF approximately 0). In general, RF depends on the oxyanion initial concentration, oxyanion nature and Ca(OH)(2) dose. The presence of oxyanions could also influence the crystal morphology and aggregation/agglomeration process. For example, a c-axis elongation of calcite crystals was clearly observed at the equilibrium, for calcite formation in presence of selenite and phosphate. The oxyanions removal process proposed herein was inspired on the common physicochemical treatment of wastewater using calcium hydroxide (Ca(OH)(2)). The particularity, for this novel method is the simultaneous calcium hydroxide carbonation with compressed carbon dioxide in order to stabilise the solid matter. This economical and ecological method could allow the removal of various oxyanions

  13. Mineralization of Calcium Carbonate on Multifunctional Peptide Assembly Acting as Mineral Source Supplier and Template.

    Science.gov (United States)

    Murai, Kazuki; Kinoshita, Takatoshi; Nagata, Kenji; Higuchi, Masahiro

    2016-09-13

    Crystal phase and morphology of biominerals may be precisely regulated by controlled nucleation and selective crystal growth through biomineralization on organic templates such as a protein. We herein propose new control factors of selective crystal growth by the biomineralization process. In this study, a designed β-sheet Ac-VHVEVS-CONH2 peptide was used as a multifunctional template that acted as mineral source supplier and having crystal phase control ability of calcium carbonate (CaCO3) during a self-supplied mineralization. The peptides formed three-dimensional nanofiber networks composed of assembled bilayer β-sheets. The assembly hydrolyzed urea molecules to one carbonate anion and two ammonium cations owing to a charge relay effect between His and Ser residues under mild conditions. CaCO3 was selectively mineralized on the peptide assembly using the generated carbonate anions on the template. Morphology of the obtained CaCO3 was fiber-like structure, similar to that of the peptide template. The mineralized CaCO3 on the peptide template had aragonite phase. This implies that CaCO3 nuclei, generated using the carbonate anions produced by the hydrolysis of urea on the surface of the peptide assembly, preferentially grew into aragonite phase, the growth axis of which aligned parallel to the direction of the β-sheet fiber axis.

  14. Influence of pulse ratio on codeposition of copper species with calcium phosphate coatings on titanium by means of electrochemically assisted deposition.

    Science.gov (United States)

    Wolf-Brandstetter, Cornelia; Oswald, Steffen; Bierbaum, Susanne; Wiesmann, Hans-Peter; Scharnweber, Dieter

    2014-01-01

    Aim of this study was to combine the well-known biocompatibility and ostoeconductivity of thin calcium phosphate coatings on titanium with proangiogenic signals from codeposited copper species. Copper species could be integrated in mineral layers based on hydroxyapatite by means of electrochemically assisted deposition from electrolytes containing calcium, phosphate, and copper ions. Different combinations of duration and intensity of galvanostatic pulses result in different amounts of deposited calcium phosphate and of copper species even for the same applied total charge. Absolute amounts of copper varied between 2.1 and 6.9 μg/cm², and the copper was distributed homogeneously as shown by EDX mapping. The presence of copper did not change the crystalline phase of deposited calcium phosphate (hydroxyapatite) but provoked a significant decrease in deposited amounts by factor 3 to 4. The copper was deposited mainly as Cu(I) species with a minor fraction of basic copper phosphates. Reduction of copper occurred not only at the surface of titanium but also within the hydroxyapatite coating due to the reaction with hydrogen produced by the electrolysis of water during the cathodic polarization of the substrate.

  15. Nitrogen and Carbon Dynamics Across Trophic Levels Along an Atmospheric Nitrogen Deposition Gradient

    Science.gov (United States)

    Wissinger, B. D.; Bell, M. D.; Newingham, B. A.

    2011-12-01

    Atmospheric nitrogen deposition has altered soil biogeochemical processes and plant communities across the United States. Prior investigations have demonstrated these alterations; however, little is known about the effects of elevated nitrogen on higher trophic levels. Building upon previous research that revealed an atmospheric nitrogen deposition gradient from the San Bernardino Mountains through Joshua Tree National Park in California, we investigated atmospheric nitrogen and its effects on soils, plants, and harvester ants. We measured nitrogen and carbon concentrations, along with carbon and nitrogen stable isotopes, across trophic levels at eighteen urban and unpopulated sites along the deposition gradient. Carbon and nitrogen attributes were determined in atmospheric nitric acid, soil, Larrea tridentata and Ambrosia dumosa leaves, seeds from selected plant species, and ants. We predicted carbon and nitrogen ratios and isotopes to change in areas with higher nitrogen deposition and vary along the deposition gradient. Nitrogen (p=0.02) and carbon (p=0.05) concentrations, as well as C:N ratios (p=<0.001), significantly differed in Messor pergandei individuals among sites; however, no correlation was found between these carbon and nitrogen attributes and the nitrogen deposition gradient (%N r2=0.02, %C r2=0.007, C:N r2=0.02). The δ15N and δ13C values of the ants, leaf tissues, and seeds measured across the gradient follow similar patterns with r2 values all below 0.20. Our results suggest the current and previous rates of nitrogen deposition in this area are not enough to modify nitrogen and carbon concentrations and isotope values. Compensatory nitrogen cycling processes in the soil may reduce the effects of increased nitrogen on plants and thus higher trophic levels. Nitrogen and carbon dynamics across trophic levels might change after longer ecosystem exposure to elevated nitrogen; however, other abiotic and biotic factors are likely driving current

  16. X-ray characteristics of wrists in calcium pyrophosphate crystal deposition disease. Is pseudogout a major cause of scapholunate advanced collapse?

    Science.gov (United States)

    Taniguchi, Y; Yoshida, M; Tamaki, T

    1997-10-01

    Deposition of calcium pyrophosphate dihydrate (CPPD) crystals has been considered to be a cause of scapholunate advanced collapse (SLAC) wrist. The aim of this study was to look at X-ray changes in wrist joints affected by CPPD crystal deposition disease and to determine whether crystal deposition is a cause of SLAC wrist. A total of 150 wrists of 78 patients with CPPD crystal deposition disease were examined. In our population of Japanese patients with CPPD crystal deposition disease, the incidence of SLAC wrist was very low, and no case of Stage III SLAC wrist was found. We therefore conclude that SLAC wrist is not a radiographic characteristic of CPPD crystal deposition disease and that pyrophosphate crystal deposition cannot be a major cause of SLAC wrist.

  17. Treatment of oil–water emulsions by adsorption onto activated carbon, bentonite and deposited carbon

    Directory of Open Access Journals (Sweden)

    Khaled Okiel

    2011-06-01

    Full Text Available Emulsified oil in waste water constitutes is a severe problem in the different treatment stages before disposed off in a manner that does not violate environmental criteria. One commonly used technique for remediation of petroleum contaminated water is adsorption. The main objective of this study is to examine the removal of oil from oil–water emulsions by adsorption on bentonite, powdered activated carbon (PAC and deposited carbon (DC. The results gave evidence of the ability of the adsorbents to adsorb oil and that the adsorptive property of the three adsorbents (bentonite, PAC, and DC has been influenced by different factors. The effects of contact time, the weight of adsorbents and the concentration of adsorbate on the oil adsorption have been studied. Oil removal percentages increase with increasing contact time and the weight of adsorbents, and decrease with increasing the concentration of adsorbate. Equilibrium studies show that the Freunlich isotherm was the best fit isotherm for oil removal by bentonite, PAC, and DC. The data show higher adsorptive capacities by DC and bentonite compared to the PAC.

  18. Evaluation of chemical and structural properties of germanium-carbon coatings deposited by plasma enhanced chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    Jamali, Hossein, E-mail: h.jamali@mut-es.ac.ir; Mozafarinia, Reza; Eshaghi, Akbar

    2015-10-15

    Germanium-carbon coatings were deposited on silicon and glass substrates by plasma enhanced chemical vapor deposition (PECVD) using three different flow ratios of GeH{sub 4} and CH{sub 4} precursors. Elemental analysis, structural evaluation and microscopic investigation of coatings were performed using laser-induced breakdown spectroscopy (LIBS), Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), Raman spectroscopy, field emission scanning electron microscopy (FESEM) and atomic force microscopy (AFM), respectively. Based on the results, the coatings exhibited a homogeneous and dense structure free of pores with a very good adhesion to substrate. The structural evaluation revealed that the germanium-carbon coatings were a kind of a Ge-rich composite material containing the amorphous and crystalline germanium and amorphous carbon with the mixture of Ge–Ge, Ge–C, C–C, Ge–H and C–H bonds. The result suggested that the amorphisation of the coatings could be increased with raising CH{sub 4}:GeH{sub 4} flow rate ratio and subsequently increasing C amount incorporated into the coating. - Highlights: • Germanium-carbon coatings were prepared by PECVD technique. • The germanium-carbon coatings were a kind of composite material. • The amorphisation of the coatings were increased with raising CH{sub 4}:GeH{sub 4} flow ratio.

  19. Exposure Assessment and Inflammatory Response Among Workers Producing Calcium Carbonate Nanomaterials

    Science.gov (United States)

    Cui, Ling

    Problem: Nanotechnology is one of the most rapidly growing fields of science and engineering, and its applications have expanded to numerous research and industrial sectors, from consumer products to medicine to energy. Nano-materials and nanotechnology promise substantial benefits. However, there are many uncertainties and concerns regarding human health and the environment. Numerous toxicological studies on animals and cells in vitro have demonstrated that nanomaterials could cause various adverse health effects, including inflammation, oxidative stress, fibrosis and mutagenesis in the lungs, and cardiovascular and nervous system impairment. Objectives: The overall objective of this study was to characterize particulate exposures in a calcium carbonate nanoparticle manufacturing facility, investigate possible respiratory and cardiovascular effects, and explore the plausibility of an inflammatory mechanism. The associations between exposure level and various health outcomes were investigated. Methodology: Each job was characterized by mass, number and surface area concentration. Job classification was performed based on ranking of the exposure level and statistical models. Lung function tests, exhaled NO and blood pressure (BP) were measured before and after the workshift in the year of 2011. Inflammatory cytokines from induced sputum were measured cross-sectionally in the year of 2011. Data of lung function tests and blood pressure were collected cross-sectionally in the year of 2012. The associations between each exposure metric and health measures in 2012 were investigated. Only mass concentration was linked to both 2011 and 2012 health outcomes. Results: The sampling and analytic methodology used in the study presents the potential to characterize nanoparticle exposure for a variety of operational processes. We found the highest mass exposure occurred at bagging job whereas the highest number and surface area concentration was found at modification

  20. A New Genetic Type of Gold Deposits-Meso-Epithermal Carbonate-Type Gold Deposits as Exemplified by the Baguamiao Suprlarge Gold Deposit

    Institute of Scientific and Technical Information of China (English)

    1995-01-01

    Gold deposits of the meso-epithermal carbonate type were first proposed based on the study of the Baguamiao gold deposit.This new type of gold deposits has many unique characteristics as follows:(1)Obviously strata-bound.The gold deposits are hosted in Middle Devonian turbidite formations;(2)Structrually controlled.Struc-ture is an important factor leading to metallogenesis of this type of gold deposits.The shape and distribution of orebodies are controlled by byittle-ductile shear zones;(3)Multi-stage wall-rock alteration.According to the characteristics of mineral assemblage,gold mineralization can be classified into three stages in association with various wall-rock al-terations.Wall-rock alterations closely genetically related to the gold mineralization are ankerization ,silicification,pyrrhotization and pyritization ;(4)Mineral compositions of the orebodies are mainly pyrrhotite,pyrite,marcasitolite,chalcopyrite,quartz,ankerite,and sericite.Gold mineralization is associated closely in space and time with iron sulfides;(5)Rare elements and REE in ores are low in contents relative to those of the crust.Au content varies from 1.91g/t to 11.15g/t ,averaging 5.5g/t;(6)Studies of sulfur,hydrogen,oxygen and carbon isotopes in main gangue minerals (quartz and ankerite)indicate that fluids and ore-forming materials came from deep-seated sources;(7)Three types of inclusions are recognized in terms of their composition and the vapor amounts of inclusions.The homogenization temperatures of inclusions range from 210℃to 310℃,averaging 230℃,showing that this type of gold deposits belongs to the meso-epithermal type;(8)Metallogenic age of this type of gold deposits is similar to that of the collision between the Yangtze Plate and the North China Plate,indicating that gold deposits of this type are genetically related to continental-margin plate activity.

  1. Synthesis and characterization of well-aligned carbon nitrogen nanotubes by microwave plasma chemical vapor deposition

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Well-aligned carbon nitrogen nanotube films have been synthesized successfully on mesoporous silica substrates by microwave plasma chemical vapor deposition (MWPCVD) method. Studies on their morphology, structure, and composition by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive X-ray spectroscopy (EDX), respectively, indicate that these nanotubes consist of linearly polymerized carbon nitrogen nanobells, and the nitrogen atoms have been doped into carbon netweork to form a new structure C1-xNx (x=0.16±0.01). X-ray photoelectron spectroscopy (XPS) results of the samples further demonstrate that carbon bonds covalently with nitrogen in all the carbon nitrogen nanotube films.

  2. Carbon nanostructures and networks produced by chemical vapor deposition

    NARCIS (Netherlands)

    Kowlgi, N.K.K.; Koper, G.J.M.; Van Raalten, R.A.D.

    2012-01-01

    The invention pertains to a method for manufacturing crystalline carbon nanostructures and/or a network of crystalline carbon nanostructures, comprising: (i) providing a bicontinuous micro-emulsion containing metal nanoparticles having an average particle size between 1and 100nm; (ii) bringing said

  3. Chemical vapor deposition fabrication and characterization of silica-coated carbon fiber ultramicroelectrodes.

    Science.gov (United States)

    Zhao, G; Giolando, D M; Kirchhoff, J R

    1995-08-01

    Carbon fiber disk ultramicroelectrodes (UMEs) with well-defined geometries were prepared by chemical vapor deposition techniques. Transparent silica films with thicknesses from 1 to 600 microns were deposited on the cylindrical length of 5 and 10 microns carbon fibers from a SiCl4, H2, and O2 ternary precursor system at 850-1150 degrees C or sequential deposition from Si(OEt)4 as a single source precursor at 700 degrees C followed by the SiCl4, H2, and O2 precursor system. Film thickness, film adhesion to the fiber substrate, and the overall dimensions of the silica-coated carbon fiber were studied and found to be a function of the precursor system, precursor concentrations, fiber diameter, deposition time, and fiber temperature. The silica films were found to be free of microcracks and characterized by a quality seal between the carbon fiber and the coating. As a result, the silica-coated disk UME exhibits an excellent electrochemical response without the need to use an epoxy sealant at the electrode tip. Furthermore, the deposition of hard and inert ceramic materials imparts durability to fragile carbon fibers and facilitates the handling of UMEs in microenvironments. Finally, the advantage of concentric deposition about the fibers to produce a disk UME in the center of an insulating plane was used to examine the effect of the thickness of the insulating coating on the limiting current response.

  4. Effect of nickel introduced by electroplating on pyrocarbon deposition of carbon-fiber preforms

    Directory of Open Access Journals (Sweden)

    Ren Yancai

    2014-08-01

    Full Text Available In order to improve the deposition rate and microstructure of pyrocarbon, nickel was introduced by electroplating on carbon fibers and used as a catalyst during the deposition of pyrocarbon at 1000 °C using methane as a precursor gas. The distribution of nickel catalyst and the microstructure of pyrocarbon were characterized by scanning electron microscopy (SEM, energy dispersive spectroscopy (EDS, X-ray diffraction (XRD, and Raman micro-spectrometry. Results show that nano-sized nickel particles could be well distributed on carbon fibers and the pyrocarbon deposited catalytically had a smaller d002 value and a higher graphitization degree compared with that without catalyst. In addition, the deposition rate of pyrocarbon in each hour was measured. The deposition rate of pyrocarbon in the first hour was more than 10 times when carbon cloth substrates were doped with nickel catalysts as compared to the pure carbon cloths. The pyrocarbon gained by rapid deposition may include two parts, which are generation directly on the nickel catalyst and formation with the carbon nanofibers as crystal nucleus.

  5. Amorphous carbon film deposition on inner surface of tubes using atmospheric pressure pulsed filamentary plasma source

    CERN Document Server

    Pothiraja, Ramasamy; Awakowicz, Peter

    2011-01-01

    Uniform amorphous carbon film is deposited on the inner surface of quartz tube having the inner diameter of 6 mm and the outer diameter of 8 mm. A pulsed filamentary plasma source is used for the deposition. Long plasma filaments (~ 140 mm) as a positive discharge are generated inside the tube in argon with methane admixture. FTIR-ATR, XRD, SEM, LSM and XPS analyses give the conclusion that deposited film is amorphous composed of non-hydrogenated sp2 carbon and hydrogenated sp3 carbon. Plasma is characterized using optical emission spectroscopy, voltage-current measurement, microphotography and numerical simulation. On the basis of observed plasma parameters, the kinetics of the film deposition process is discussed.

  6. Fabrication of Pt deposited on carbon nanotubes and performance of its polymer electrolyte membrane fuel cells

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A new method of depositing nano-sized Pt particles on the surface of the carbon nano-tubes was introduced, and the performance of Pt/carbon nanotube compound on polymer electrolyte membrane fuel cells was measured. The experimental results show that the fine platinum particles (about 3 nm) were well dispersed on carbon nanotubes, which demonstrates the excellent catalytic properties of the Pt/CNTs compound in polymer electrolyte membrane fuel cells.

  7. Influence of carbon nanotubes coatings onto carbon fiber by oxidative treatments combined with electrophoretic deposition on interfacial properties of carbon fiber composite

    Science.gov (United States)

    Deng, Chao; Jiang, Jianjun; Liu, Fa; Fang, Liangchao; Wang, Junbiao; Li, Dejia; Wu, Jianjun

    2015-12-01

    To improve the interfacial performance of carbon fiber (CF) and epoxy resin, carbon nanotubes (CNTs) coatings were utilized to achieve this purpose through coating onto CF by the treatment with hydrogen peroxide and concentrated nitric acid combined with electrophoretic deposition (EPD) process. The influence of electrophoretically deposited CNTs coatings on the surface properties of CFs were investigated by Fourier transform infrared spectrometer, atomic force microscopy, scanning electron microscopy and dynamic contact angle analysis. The results indicated that the deposition of carbon nanotubes introduced some polar groups to carbon fiber surfaces, enhanced surface roughness and changed surface morphologies of carbon fibers. Surface wettability of carbon fibers may be significantly improved by increasing surface free energy of the fibers due to the deposition of CNTs. The thickness and density of the coatings increases with the introduction of pretreatment of the CF during the EPD process. Short beam shear test was performed to examine the effect of carbon fiber functionalization on mechanical properties of the carbon fiber/epoxy resin composites. The interfacial adhesion of CNTs/CF reinforced epoxy composites showed obvious enhancement of interlaminar shear strength by 60.2% and scanning electron microscope photographs showed that the failure mode of composites was changed after the carbon fibers were coated with CNTs.

  8. Dust deposition in an oligotrophic marine environment: impact on the carbon budget

    Directory of Open Access Journals (Sweden)

    C. Guieu

    2014-01-01

    Full Text Available By bringing new nutrients and particles to the surface ocean, atmospheric deposition impacts biogeochemical cycles. The extent to which those changes are modifying the carbon balance in oligotrophic environments such as the Mediterranean Sea that receives important Saharan dust fluxes is unknown. DUNE project provides the first attempt to evaluate the changes induced in the carbon budget of an oligotrophic system after simulated Saharan dust wet and dry deposition events. Here we report the results for the 3 distinct artificial dust seeding experiments in large mesocosms that were conducted in the oligotrophic waters of the Mediterranean Sea in summer 2008 and 2010. Simultaneous measurements of the metabolic rates (C fixation, C respiration in the water column have shown that the dust deposition did not change drastically the metabolic balance as the tested waters remained net heterotroph (i.e. net primary production to bacteria respiration ratio < 1 and in some cases the net heterotrophy was even enhanced by the dust deposition. Considering the different terms of the carbon budget, we estimate that it was balanced with a dissolved organic carbon (DOC consumption of at least 10% of the initial stock. This corresponds to a fraction of the DOC stock of the surface mixed layer that consequently will not be exported during the winter mixing. Although heterotrophic bacteria were found to be the key players in the response to dust deposition, net primary production increased about twice in case of simulated wet deposition (that includes anthropogenic nitrogen and a small fraction of particulate organic carbon was still exported. Our estimated carbon budgets are an important step forward in the way we understand dust deposition and associated impacts on the oceanic cycles. They are providing knowledge about the key processes (i.e. bacteria respiration, aggregation that need to be considered for an integration of atmospheric deposition in marine

  9. The preparation of 248CmF 3 deposits on self-supported carbon foils

    Science.gov (United States)

    Aaron, W. S.; Petek, M.; Zevenbergen, L. A.

    1987-06-01

    Another target preparative technique was recently added to the Isotope Research Materials Laboratory's (IRML) capabilities for custom target fabrication. In support of super-heavy-ion physics experiments, methods and equipment were developed for the preparation of 248CmF 3 deposits on carbon foils. The starting material was obtained as either a chloride or nitrate solution, converted to the flouride, and evaporated on carbon foil substrates. Deposits ranging from 40 to 570 μg/cm 2 were prepared as a 12-mm-diam spot on 45- to 60-μg/cm 2 self-supported carbon foils. The deposits were then overcoated with approximately 10 μg/cm 2 of carbon to minimize contamination problems during target handling. The high cost of 248Cm ($100/μg) and its limited availability were the key constraints in the development of preparative technology beyond the inherent radioactivity of 248Cm.

  10. Rapid Carbonate Depositional Changes Following the Permian-Triassic Mass Extinction:Sedimentary Evidence from South China

    Institute of Scientific and Technical Information of China (English)

    Li Tian; Jinnan Tong; David Bottjer; Daoliang Chu; Lei Liang; Huyue Song; Haijun Song

    2015-01-01

    Various environmental changes were associated with the Permian-Triassic mass extinc-tion at 252.2 Ma. Diverse unusual sediments and depositional phenomena have been uncovered as re-sponses to environmental and biotic changes. Lithological and detailed conodont biostratigraphic cor-relations within six Permian-Triassic boundary sections in South China indicate rapid fluctuations in carbonate deposition. Four distinct depositional phases can be recognized:(1) normal carbonate depo-sition on the platform and slope during the latest Permian;(2) reduced carbonate deposition at the on-set of the main extinction horizon; (3) expanded areas of carbonate deposition during the Hindeodus changxingsensis Zone to the H. parvus Zone;and (4) persistent mud-enriched carbonate deposition in the aftermath of the Permian-Triassic transition. Although availability of skeletal carbonate was sig-nificantly reduced during the mass extinction, the increase in carbonate deposition did not behave the same way. The rapid carbonate depositional changes, presented in this study, suggest that diverse envi-ronmental changes played key roles in the carbonate deposition of the Permian-Triassic mass extinction and onset of its aftermath. An overview of hypotheses to explain these changes implies enhanced terres-trial input, abnormal ocean circulation and various geobiological processes contributed to carbonate saturation fluctuations, as the sedimentary response to large volcanic eruptions.

  11. Oxidation Protection Systems for Carbon-Carbon Composites Formed by Chemical Vapor Deposition and Plasma Assisted Chemical Vapor Deposition Techniques

    Science.gov (United States)

    1992-04-22

    transducer, ie. a more positive scaleI I 34 thickness of fairly continuous conversion layer carbon 10 , •O.0000 resina 0 0 Fiber O0c00.a 0 Bundlea • 06...thermal and oxidative environments. It should meet four main requirements: adequate adhesion between substrate and coating; maximum resistance to...resistance and good coating adhesion . (2) CVD Coatings I Currently, the most successful protective coating for carbon-carbon composite is CVD SiC. Coatings

  12. Effects of Calcium Carbonate on Pain Symptoms in Third Trimester of Pregnancy and Nursing Period: a randomized clinical trial

    Directory of Open Access Journals (Sweden)

    Soosan Alimohammadzadeh Taher

    2008-06-01

    Full Text Available Objective: The study evaluated the efficacy of oral calcium carbonate supplement on leg pain in pregnancy and nursing period.Materials and methods: A total number of 176 women at third trimester of pregnancy or nursing period till to one year after delivery with complaint of leg pain, low back pain (LBP, and posterior pelvic pain (PPP were evaluated for distinct primary causes and were excluded, then 58 patients randomized into calcium group (n=27 treated with 500 mg calcium carbonate orally per day just for one week, and control group (n=31 received no drug. Incidence of days with leg, low back, and posterior pelvic pain per week were evaluated and compared between the two groups at 3 different weeks before, during, and after discontinuation of drug. Statistical significance was defined as P<0.05.  Results: Mean number of days with leg pain per week during calcium carbonate intake was significantly different between the study and control groups (P<0.05. Mean number of days with LBP and PPP was not significantly different between two groups.Conclusion: The use of oral calcium supplement was associated with lower episodes of leg pain but failed to reduce the incidence of LBP and PPP in pregnancy and nursery period.

  13. Deposition rate and morphology of carbon nanotubes at different positions in a CVD reactor

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Carbon nanotubes (CNTs) were synthesized through the catalytic decomposition of a ferroeene-xylene mixture in a horizontal chemical vapor deposition reactor.The deposition rate of CNTs along the axial direction was measured.The morphology of CNTs was observed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM).The results showed that the deposition rate of CNTs along the axial direction first increased and later decreased,the position achieving the maximum deposition rate was influenced by the operating conditions.The morphologies of CNTs also changed along the axial direction.

  14. Effects of nitrogen deposition on carbon cycle in terrestrial ecosystems of China

    DEFF Research Database (Denmark)

    Chen, Hao; Li, Dejun; Gurmesa, Geshere Abdisa

    2015-01-01

    Nitrogen (N) deposition in China has increased greatly, but the general impact of elevated N deposition on carbon (C) dynamics in Chinese terrestrial ecosystems is not well documented. In this study we used a meta-analysis method to compile 88 studies on the effects of N deposition C cycling...... and rate of N addition. Overall, our findings suggest that 1) decreased below-ground plant C pool may limit long-term soil C sequestration; and 2) it is better to treat N-rich and N-limited ecosystems differently in modeling effects of N deposition on ecosystem C cycle....

  15. CONFORMATION AND MICROSTRUCTURE OF CARBON NANOFIBERS DEPOSITED ON FOAM Ni

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Bundles of pure carbon nanofibers were prepared by catalytic decomposition of acetylene on foam Ni. The morphological and structural characteristics of the carbon nanostructures, in the as-prepared state, were analyzed by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and high resolution transmission electron microscopy (HTEM). A special conformation of carbon nanofibers composed of segmented structures was found among the products by both SEM and TEM observations. Further HTEM ex amination indicated that the segments were stacked with well ordered graphite platelets arranged perpendicular to the axis of the filaments.

  16. Dissolution and storage stability of nanostructured calcium carbonates and phosphates for nutrition

    Science.gov (United States)

    Posavec, Lidija; Knijnenburg, Jesper T. N.; Hilty, Florentine M.; Krumeich, Frank; Pratsinis, Sotiris E.; Zimmermann, Michael B.

    2016-10-01

    Rapid calcium (Ca) dissolution from nanostructured Ca phosphate and carbonate (CaCO3) powders may allow them to be absorbed in much higher fraction in humans. Nanosized Ca phosphate and CaCO3 made by flame-assisted spray pyrolysis were characterized by nitrogen adsorption, X-ray diffraction (XRD), Raman spectroscopy, and transmission electron microscopy. As-prepared nanopowders contained both CaCO3 and CaO, but storing them under ambient conditions over 130 days resulted in a complete transformation into CaCO3, with an increase in both crystal and particle sizes. The small particle size could be stabilized against such aging by cation (Mg, Zn, Sr) and anion (P) doping, with P and Mg being most effective. Calcium phosphate nanopowders made at Ca:P ≤ 1.5 were XRD amorphous and contained γ-Ca2P2O7 with increasing hydroxyapatite content at higher Ca:P. Aging of powders with Ca:P = 1.0 and 1.5 for over 500 days gradually increased particle size (but less than for CaCO3) without a change in phase composition or crystallinity. In 0.01 M H3PO4 calcium phosphate nanopowders dissolved ≈4 times more Ca than micronsized compounds and about twice more Ca than CaCO3 nanopowders, confirming that nanosizing and/or amorphous structuring sharply increases Ca powder dissolution. Because higher Ca solubility in vitro generally leads to greater absorption in vivo, these novel FASP-made Ca nanostructured compounds may prove useful for nutrition applications, including supplementation and/or food fortification.

  17. A mixed flow reactor method to synthesize amorphous calcium carbonate under controlled chemical conditions.

    Science.gov (United States)

    Blue, Christina R; Rimstidt, J Donald; Dove, Patricia M

    2013-01-01

    This study describes a new procedure to synthesize amorphous calcium carbonate (ACC) from well-characterized solutions that maintain a constant supersaturation. The method uses a mixed flow reactor to prepare ACC in significant quantities with consistent compositions. The experimental design utilizes a high-precision solution pump that enables the reactant solution to continuously flow through the reactor under constant mixing and allows the precipitation of ACC to reach steady state. As a proof of concept, we produced ACC with controlled Mg contents by regulating the Mg/Ca ratio of the input solution and the carbonate concentration and pH. Our findings show that the Mg/Ca ratio of the reactant solution is the primary control for the Mg content in ACC, as shown in previous studies, but ACC composition is further regulated by the carbonate concentration and pH of the reactant solution. The method offers promise for quantitative studies of ACC composition and properties and for investigating the role of this phase as a reactive precursor to biogenic minerals.

  18. Electrolytic deposition of calcium phosphate/chitosan coating on titanium alloy: Growth kinetics and influence of current density, acetic acid, and chitosan

    NARCIS (Netherlands)

    Wang, Jiawei; Apeldoorn, van Aart; Groot, de Klaas

    2006-01-01

    Electrolytically deposited calcium phosphate/chitosan coating demonstrated good bone marrow stromal cell attachment. The aim of this study was to understand the coating's growth kinetics as well as the effects of current density, acetic acid, and chitosan on the coating's formation. The scanning ele

  19. Influence of acid-soluble proteins from bivalve Siliqua radiata ligaments on calcium carbonate crystal growth

    Science.gov (United States)

    Huang, Zeng-Qiong; Zhang, Gang-Sheng

    2016-08-01

    In vitro biomimetic synthesis of calcium carbonate (CaCO3) in the presence of shell proteins is a heavily researched topic in biomineralization. However, little is known regarding the function of bivalve ligament proteins in the growth of CaCO3 crystals. In this study, using fibrous protein K58 from Siliqua radiata ligaments or coverslips as substrates, we report the results of our study of CaCO3 precipitation in the presence or absence of acid-soluble proteins (ASP) from inner ligament layers. ASP can disturb the controlling function of K58 or a coverslip on the crystalline phase, resulting in the formation of aragonite, calcite, and vaterite. In addition, we identified the following four primary components from ASP by mass spectroscopy: alkaline phosphatase (ALP), ABC transporter, keratin type II cytoskeletal 1 (KRT 1), and phosphate ABC transporter, phosphate-binding protein (PstS). Further analysis revealed that the first three proteins and especially ALP, which is important in bone mineralisation, could affect the polymorphism and morphology of CaCO3 crystals by trapping calcium ions in their domains. Our results indicate that ALP may play an important role in the formation of aragonite in S. radiata ligaments. This paper may facilitate our understanding of the biomineralization process.

  20. Introduction of enzymatically degradable poly(trimethylene carbonate) microspheres into an injectable calcium phosphate cement.

    Science.gov (United States)

    Habraken, Wouter J E M; Zhang, Zheng; Wolke, Joop G C; Grijpma, Dirk W; Mikos, Antonios G; Feijen, Jan; Jansen, John A

    2008-06-01

    Poly(trimethylene carbonate) (PTMC) is an enzymatically degradable polyester with rubber-like properties. Introduction of this polymer into an injectable calcium phosphate bone cement can therefore be used to introduce macroporosity into the cement for tissue engineering purposes as well as to improve mechanical properties. Aim of this study was to investigate calcium phosphate cements with incorporated PTMC microspheres (PTMC CPCs) on their physical/mechanical properties and in vitro degradation characteristics. Therefore, composites were tested on setting time and mechanical strength as well as subjected to phosphate buffered saline (PBS) and enzyme containing medium. PTMC CPCs (12.5 and 25 wt%) with molecular weights of 52.7 kg mol(-1) and 176.2 kg mol(-1) were prepared, which showed initial setting times similar to that of original CPC. Though compression strength decreased upon incorporation of PTMC microspheres, elastic properties were improved as strain-at-yield increased with increasing content of microspheres. Sustained degradation of the microspheres inside PTMC CPC occurred when incubated in the enzymatic environment, but not in PBS, which resulted in an interconnected macroporosity for the 25 wt% composites.

  1. Calcium carbonate formation on mica supported extracellular polymeric substance produced by Rhodococcus opacus

    Science.gov (United States)

    Szcześ, Aleksandra; Czemierska, Magdalena; Jarosz-Wilkołazka, Anna

    2016-10-01

    Extracellular polymeric substance (EPS) extracted from Rhodococcus opacus bacterial strain was used as a matrix for calcium carbonate precipitation using the vapour diffusion method. The total exopolymer and water-soluble exopolymer fraction of different concentrations were spread on the mica surface by the spin-coating method. The obtained layers were characterized using the atomic force microscopy measurement and XPS analysis. The effects of polymer concentration, initial pH of calcium chloride solution and precipitation time on the obtained crystals properties were investigated. Raman spectroscopy and scanning electron microscopy were used to characterize the precipitated minerals. It was found that the type of precipitated CaCO3 polymorph and the crystal size depend on the kind of EPS fraction. The obtained results indicates that the water soluble fraction favours vaterite dissolution and calcite growth, whereas the total EPS stabilizes vaterite and this effect is stronger at basic pH. It seems to be due to different contents of the functional group of EPS fractions.

  2. Structure and phase composition of deposited tantalum-carbon films

    Science.gov (United States)

    Tuleushev, Yu. Zh.; Volodin, V. N.; Zhakanbaev, E. A.; Alimzhan, B.

    2016-08-01

    Ion plasma sputtering and the subsequent codeposition of ultrafine tantalum and carbon particles were used to prepare coatings with 4.6-71.5 at % C. Structural studies of the coatings showed the existence of carbon solid solutions in β Ta at carbon contents to 4.6 at %, carbon solid solutions in α Ta at carbon contents of 4.6-10.3 at %, and direct synthesis of TaC at carbon contents of 44.7-71.5 at %. During heat treatments to 700°C, the substantial concentration widening of regions of the existence of Ta2C and TaC was found. The lattice parameters of hexagonal Ta2C and fcc TaC carbides were determined for composition ranges of the existence of phases during heating to 700°C. Upon heating above 600°C, the progressive transition of quasiamorphous Ta2C carbide into the crystalline Ta2C carbide was found to take place. The possibility of applying the direct synthesis of TaC carbide in engineering was noted.

  3. INFLUENCE OF SURFACE-MODIFICATION FOR CALCIUM CARBONATE ON THE INTERACTION BETWEEN THE FILLERS AND POLYDIMETHYLSILOXANE

    Institute of Scientific and Technical Information of China (English)

    Xiao-ming Xu; Xiao-le Tao; Qiang Zheng

    2008-01-01

    The surface of calcium carbonate (CaCO3) particles was modified with stearic acid (SA) and the chemicalstructures of the product were characterized by FT-IR analysis. The interaction between polydimethylsiloxane (PDMS) andCaCO3 fillers with different surface character was investigated by means of dynamic rheologicai and bound rubber tests foruncured compounds and mechanical properties measurements for the corresponding vulcanites. The results of dynamic testsindicate that with the increase of SA mass fraction, the span of the linear viscoelastic region broadens and the height of themodulus plateau decreases. The reasons for these are ascribed to that the SA decreases the surface energy of filler particlesand weakens their tendency to agglomerate. Moreover, the results of mechanical measurements reveal that the vulcanizedcompound filled with modified filler has a relative high tensile strength induced by a reinforced interaction between fillerand polymer matrix, which is confirmed by the bound rubber tests and transmission electron microscopy (TEM) observations.

  4. Preparation of poly (methyl methacrylate)/nanometer calcium carbonate composite by in-situ emulsion polymerization

    Institute of Scientific and Technical Information of China (English)

    史建明; 包永忠; 黄志明; 翁志学

    2004-01-01

    Methyl methacrylate (MMA) emulsion polymerization in the presence of nanometer calcium carbonate (nano-CaCO3) surface modified with (-methacryloxypropyltrimethoxysilane (MPTMS) was carried out to prepare poly (methyl methacrylate) (PMMA)/nano-CaCO3 composite. The reaction between nano-CaCO3 and MPTMS, and the grafting of PMMA onto nano-CaCO3 were confirmed by infrared spectrum. The grafting ratio and grafting efficiency of PMMA on nano-CaCO3 modified with MPTMS were much higher than that on nano-CaCO3 modified with stearic acid. The grafting ratio of PMMA increased as the weight ratio between MMA and nano-CaCO3 increased, while the grafting efficiency of PMMA decreased. Transmission electron micrograph showed that nano-CaCO3 covered with PMMA was formed by in-situ emulsion polymerization.

  5. Effect of precipitated calcium carbonate--Cellulose nanofibrils composite filler on paper properties.

    Science.gov (United States)

    He, Ming; Cho, Byoung-Uk; Won, Jong Myoung

    2016-01-20

    A new concept of composite filler was developed by using cellulose nanofibrils (CNF), precipitated calcium carbonate (PCC) and cationic starch (C-starch). In this study, cellulose nanofibrils were utilized in two different ways: a PCC-CNF composite filler and a papermaking additive in sheet forming. The aim was to elucidate their effects on flocculation, filler retention and the strength and optical properties of handsheets. The highest filler retention was obtained by using the PCC-CNF composite filler in paper sheets. The paper filled with the composite fillers had much higher bursting and tensile strengths than conventional PCC loading. It was also found that the paper prepared with PCC-CNF composite fillers became denser with increasing the filler content of paper.

  6. Physico-chemical analysis of flexible polyurethane foams containing commercial calcium carbonate

    Directory of Open Access Journals (Sweden)

    Sabrina Sá e Sant'Anna

    2008-12-01

    Full Text Available Calcium carbonate (CaCO3 is a filler often utilized by the Brazilian mattress factories in the production of polyurethane foams. The filler allows the substitution of part of the polymeric agents, conferring dimensional stability and hardness to the foams. However, in agreement with experimental data, it is observed that the excess of commercial CaCO3 utilized in industry causes the increase of hysteresis, possibly causing permanent deformations and damaging the quality of the final product. In the present work, the physico-chemical analyses of the flexible polyurethane foams with different contents of CaCO3 were performed. The foams are submitted to the morphological, mechanical and positron analyses to verify the alterations provoked by the progressive introduction of this filler.

  7. A New Method for Descaling Wool Fibres by Nano Abrasive Calcium Carbonate Particles in Ultrasonic Bath

    Directory of Open Access Journals (Sweden)

    Ali rezaghasemi

    2016-08-01

    Full Text Available Up to now, the most conventional methods for descaling of wool fibre are based on chemical degradation and resin covering of scales or a combination of them. These methods are producing wastewater and can cover physical properties of the fibres beside scales orderly. In this study, a new and clean method is developed on the basis of abrasion effect of calcium carbonate Nano particles (CCNP in an ultrasonic bath. Woolen Samples (fibre and yarn were sonicated with different levels of CCNP. Tensile properties of the yarns, directional friction effect of the fibres and scanning electron microscope images of the fibres were studied. Test results showed that sonicated Nano treatment of woolyarn reduced its tenacity, extension and work of rupture and increased its coefficient of friction. Scanning electron microscope images of fibres and measurement of fibres directional displacement confirmed descaling of Nano abrasive treated wool samples in comparison to the raw wool.

  8. Nanoplasmonic smooth silica versus porous calcium carbonate bead biosensors for detection of biomarkers

    Energy Technology Data Exchange (ETDEWEB)

    Yashchenok, A.M.; Borisova, D.; Pinchasik, B.; Moehwald, H. [Department of Interfaces, Max Planck Institute of Colloids and Interfaces, 14424 Potsdam (Germany); Parakhonskiy, B.V. [BIOtech center, University of Trento, 38123 Mattarello (Italy); Shubnikov Institute of Crystallography, Russian Academy of Science, Moscow (Russian Federation); Masic, A. [Department of Biomaterials, Max Planck Institute of Colloids and Interfaces, 14424 Potsdam (Germany); Skirtach, A.G. [Department of Interfaces, Max Planck Institute of Colloids and Interfaces, 14424 Potsdam (Germany); Department of Molecular Biotechnology, Ghent University, 9000 Ghent, and Nano-Bio (NB)-Photonics, Ghent University, 9000 Ghent (Belgium)

    2012-11-15

    Nanoplasmonic biosensors based on gold nanoparticle functionalized smooth silica and porous calcium carbonate particles are presented. It is identified in this comparative study the role of porosity for adsorbing gold nanoparticles and subsequent detection of biomarkers. That is further applied in this study for detection of biomarkers. Detection of glucose - a biomarker of diabetes is studied together with that of bovine serum albumin - a very relevant bio-molecule. Raman scattering is used for label-free detection of molecules in the sub-{mu}M-mM range detection capabilities, which covers the range corresponding to healthy and diseased persons. Implications of current study for detection and identification of biomarkers are discussed. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  9. Heterogeneous reactions of gaseous methanesulfonic acid with calcium carbonate and kaolinite particles

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Heterogeneous reactions of gaseous methanesulfonic acid (MSA) with calcium carbonate (CaCO3) and kaolinite particles at room temperature were investigated using diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and ion chromatography (IC).Methanesulfonate (MS-) was identified as the product in the condensed phase,in accordance with the product of the reaction of gaseous MSA with NaCl and sea salt particles.When the concentration of gaseous MSA was 1.34 × 10-13 molecules cm-3,the uptake coefficient was (1.21 ± 0.06) × 10-8 (1) for the reaction of gaseous MSA with CaCO3 and (4.10 ± 0.65) × 10 10 (1) for the reaction with kaolinite.Both uptake coefficients were significantly smaller than those of the reactions of gaseous MSA with NaCl and sea salt particles.

  10. Influence of active sites organisation on calcium carbonate formation at model biomolecular interfaces

    Science.gov (United States)

    Hacke, S.; Möbius, D.; Lieu, V.-T.

    2005-06-01

    In an approach to understand the influence of structural parameters of interfaces on calcification in biomineralisation, the distribution and conformation of head groups as active sites in an inert matrix were varied using two-component phospholipid model monolayers. Dimyristoylphosphatidic acid (DMPA) and dipalmitoylphosphatidylcholin (DPPC), respectively, were the active components, and methyl octadecanoate (MOD) was used as inactive matrix. Surface pressure-area isotherms provide evidence for a different distribution of the active components in the matrix. Formation of solid calcium carbonate with two-component monolayers on subphases containing aqueous CaCO 3 was observed in situ by Brewster angle microscopy, where CaCO 3 domains appear bright. Striking differences in kinetics and extent of CaCO 3 formation are observed between monolayers containing dimyristoylphosphatidic acid and those containing dipalmitoylphosphatidylcholin. The presence of κ-carrageenan in the subphase as a further active component resulted in partial inhibition of CaCO 3 formation.

  11. Synthesis of calcium carbonate using extract components of croaker gill as morphology and polymorph adjust control agent.

    Science.gov (United States)

    Chen, Hao; Qing, Chengsong; Zheng, Jiaoling; Liu, Yuxi; Wu, Gang

    2016-06-01

    Biomimetic synthesis of calcium carbonate with various polymorphs, sizes and morphologies by using organic substrates has become an interesting topic for the last years. Calcium carbonate has been synthesized by the reaction of Na2CO3 and CaCl2 in the presence of extract components of croaker gill. The products were characterized by powder X-ray diffraction (PXRD) and Fourier transform infrared (FT-IR) spectrum, and particle morphologies were observed by scanning electron microscope (SEM). The results show that at lower concentration yellow croaker gill extract has no effect on calcium carbonate crystal polymorph. Calcite was obtained only. But the morphologies of calcite particle change with the increase of the concentration. The corners of the particle change from angular to curved. However, with the further increase of the concentration of yellow croaker gill extract, the calcium carbonate obtained is a mixture of calcite and vaterite. The vaterite component in the mixture rises with increasing concentration of extract solution, indicating that the proteins from the yellow croaker gill during growth play a crucial role in stabilizing and directing the crystal growth.

  12. Effect of pH and phosphate on calcium carbonate polymorphs precipitated at near-freezing temperature

    NARCIS (Netherlands)

    Hu, Yu-Bin; Wolthers, Mariëtte; Wolf-Gladrow, Dieter A.; Nehrke, Gernot

    2015-01-01

    The effects of pH and phosphate on the precipitation of calcium carbonate polymorphs from aqueous solution were investigated. Experiments were carried out at near-freezing temperature and two different pH conditions (pH 13.4 and 9.0). At each pH condition, solutions having different concentrations o

  13. Influence of calcium carbonate on extraction yield and quality of extra virgin oil from olive (Olea europaea L. cv. Coratina).

    Science.gov (United States)

    Squeo, G; Silletti, R; Summo, C; Paradiso, V M; Pasqualone, A; Caponio, F

    2016-10-15

    The aim of the research was to evaluate the effect of calcium carbonate (1%, 2%, and 4% of addition) at two different particle sizes (2.7μm and 5.7μm), added at the beginning of the malaxation phase, on both the extraction yield and the quality of oil obtained from Coratina olives at different ripening index. The results showed that calcium carbonate significantly increased the extraction yield of olive oil, more than affecting chemical indices. In particular, for less ripened olives, 1-2% of larger particle size calcium carbonate addiction determined a significant increase of the extraction effectiveness, ranging from 4.0 to 4.9%, while more ripened olives required higher amounts of coadjuvant (2-4% when using the larger particle size and 4% when using the smaller one), with a significant increase of the extraction yield up to 5%. Moreover, an increase of pungent perception was observed in some cases when adding calcium carbonate to more ripened olives.

  14. A strategy of precipitated calcium carbonate (CaCO{sub 3}) fillers for enhancing the mechanical properties of polypropylene polymers

    Energy Technology Data Exchange (ETDEWEB)

    Thenepalli, Thriveni; Ahn, Ji Whan [Korea Institute of Geoscience and Mineral Resources (KIGAM), Daejeon (Korea, Republic of); Ahn, Young Jun; Han, Choon [Kwangwoon University, Seoul (Korea, Republic of); Ramakrishna, Chilakala [Hanil Cement, Danyang (Korea, Republic of)

    2015-06-15

    A wide variety of fillers are currently used in more than twenty types of polymer resins, although four of them alone (polypropylene, polyamides, thermoplastic polyesters, and polyvinyl chloride) account for 90% of the market of mineral fillers in plastics. Polypropylene (PP) and PVC dominate the market for calcium carbonate. PP is a versatile reinforcement material that can meet engineering and structural specifications and is widely used for automotive components, home appliances, and industrial applications. Talc, mica, clay, kaolin, wollastonite, calcium carbonates, feldspar, aluminum hydroxide, glass fibers, and natural fibers are commonly used in fillers. Among these, calcium carbonate (both natural and synthetic) is the mos abundant and affords the possibility of improved surface finishing, control over the manufacture of products, and increased electric resistance and impact resistance. Meeting the global challenge to reduce the weight of vehicles by using plastics is a significant issue. The current the global plastic and automobile industry cannot survive without fillers, additives, and reinforcements. Polypropylene is a major component of the modern plastic industry, and currently is used in dashboards, wheel covers, and some engine parts in automobiles. This article reports that the use of calcium carbonate fillers with polypropylene is the best choice to enhance the mechanical properties of plastic parts used in automobiles.

  15. Calcium Carbonate Precipitation by Bacillus and Sporosarcina Strains Isolated from Concrete and Analysis of the Bacterial Community of Concrete.

    Science.gov (United States)

    Kim, Hyun Jung; Eom, Hyo Jung; Park, Chulwoo; Jung, Jaejoon; Shin, Bora; Kim, Wook; Chung, Namhyun; Choi, In-Geol; Park, Woojun

    2016-03-01

    Microbially induced calcium carbonate precipitation (CCP) is a long-standing but re-emerging environmental engineering process for production of self-healing concrete, bioremediation, and long-term storage of CO2. CCP-capable bacteria, two Bacillus strains (JH3 and JH7) and one Sporosarcina strain (HYO08), were isolated from two samples of concrete and characterized phylogenetically. Calcium carbonate crystals precipitated by the three strains were morphologically distinct according to field emission scanning electron microscopy. Energy dispersive X-ray spectrometry mapping confirmed biomineralization via extracellular calcium carbonate production. The three strains differed in their physiological characteristics: growth at alkali pH and high NaCl concentrations, and urease activity. Sporosarcina sp. HYO08 and Bacillus sp. JH7 were more alkali- and halotolerant, respectively. Analysis of the community from the same concrete samples using barcoded pyrosequencing revealed that the relative abundance of Bacillus and Sporosarcina species was low, which indicated low culturability of other dominant bacteria. This study suggests that calcium carbonate crystals with different properties can be produced by various CCP-capable strains, and other novel isolates await discovery.

  16. Atmospheric deposition as a source of carbon and nutrients to barren, alpine soils of the Colorado Rocky Mountains

    Directory of Open Access Journals (Sweden)

    N. Mladenov

    2012-03-01

    Full Text Available Many alpine areas are experiencing intense deglaciation, biogeochemical changes driven by temperature rise, and changes in atmospheric deposition. There is mounting evidence that the water quality of alpine streams may be related to these changes, including rising atmospheric deposition of carbon (C and nutrients. Given that barren alpine soils can be severely C limited, we evaluated the magnitude and chemical quality of atmospheric deposition of C and nutrients to an alpine site, the Green Lake 4 catchment in the Colorado Rocky Mountains. Using a long term dataset (2002–2010 of weekly atmospheric wet deposition and snowpack chemistry, we found that volume weighted mean dissolved organic carbon (DOC concentrations were approximately 1.0 mg L−1and weekly concentrations reached peaks as high at 6–10 mg L−1 every summer. Total dissolved nitrogen concentration also peaked in the summer, whereas total dissolved phosphorus and calcium concentrations were highest in the spring. Relationships among DOC concentration, dissolved organic matter (DOM fluorescence properties, and nitrate and sulfate concentrations suggest that pollutants from nearby urban and agricultural sources and organic aerosols derived from sub-alpine vegetation may influence high summer DOC wet deposition concentrations. Interestingly, high DOC concentrations were also recorded during "dust-in-snow" events in the spring. Detailed chemical and spectroscopic analyses conducted for samples collected in 2010 revealed that the DOM in many late spring and summer samples was less aromatic and polydisperse and of lower molecular weight than that of winter and fall samples and, therefore, likely to be more bioavailable to microbes in barren alpine soils. Bioavailability experiments with different types of atmospheric C sources are needed to better evaluate the substrate quality of atmospheric C inputs. Our C budget estimates for the Green Lake 4 catchment suggest

  17. The Influence of Electrolytic Concentration on the Electrochemical Deposition of Calcium Phosphate Coating on a Direct Laser Metal Forming Surface

    Directory of Open Access Journals (Sweden)

    Qianyue Sun

    2017-01-01

    Full Text Available A calcium phosphate (CaP coating on titanium surface enhances its biocompatibility, thus facilitating osteoconduction and osteoinduction with the inorganic phase of the human bone. Electrochemical deposition has been suggested as an effective means of fabricating CaP coatings on porous surface. The purpose of this study was to develop CaP coatings on a direct laser metal forming implant using electrochemical deposition and to investigate the effect of electrolytic concentration on the coating’s morphology and structure by X-ray diffraction, scanning electron microscopy, water contact angle analysis, and Fourier transform infrared spectroscopy. In group 10−2, coatings were rich in dicalcium phosphate, characterized to be thick, layered, and disordered plates. In contrast, in groups 10−3 and 10−4, the relatively thin and well-ordered coatings predominantly consisted of granular hydroxyapatite. Further, the hydrophilicity and cell affinity were improved as electrolytic concentration increased. In particular, the cells cultured in group 10−3 appeared to have spindle morphology with thick pseudopodia on CaP coatings; these spindles and pseudopodia strongly adhered to the rough and porous surface. By analyzing and evaluating the surface properties, we provided further knowledge on the electrolytic concentration effect, which will be critical for improving CaP coated Ti implants in the future.

  18. The Influence of Electrolytic Concentration on the Electrochemical Deposition of Calcium Phosphate Coating on a Direct Laser Metal Forming Surface

    Science.gov (United States)

    Yang, Yuhui; Luo, Wenjing

    2017-01-01

    A calcium phosphate (CaP) coating on titanium surface enhances its biocompatibility, thus facilitating osteoconduction and osteoinduction with the inorganic phase of the human bone. Electrochemical deposition has been suggested as an effective means of fabricating CaP coatings on porous surface. The purpose of this study was to develop CaP coatings on a direct laser metal forming implant using electrochemical deposition and to investigate the effect of electrolytic concentration on the coating's morphology and structure by X-ray diffraction, scanning electron microscopy, water contact angle analysis, and Fourier transform infrared spectroscopy. In group 10−2, coatings were rich in dicalcium phosphate, characterized to be thick, layered, and disordered plates. In contrast, in groups 10−3 and 10−4, the relatively thin and well-ordered coatings predominantly consisted of granular hydroxyapatite. Further, the hydrophilicity and cell affinity were improved as electrolytic concentration increased. In particular, the cells cultured in group 10−3 appeared to have spindle morphology with thick pseudopodia on CaP coatings; these spindles and pseudopodia strongly adhered to the rough and porous surface. By analyzing and evaluating the surface properties, we provided further knowledge on the electrolytic concentration effect, which will be critical for improving CaP coated Ti implants in the future. PMID:28250771

  19. Constraining the cause of the end-Guadalupian extinction with coupled records of carbon and calcium isotopes

    Science.gov (United States)

    Jost, Adam B.; Mundil, Roland; He, Bin; Brown, Shaun T.; Altiner, Demir; Sun, Yadong; DePaolo, Donald J.; Payne, Jonathan L.

    2014-06-01

    A negative δC13 excursion in carbonate sediments near the Guadalupian/Lopingian (Middle/Late Permian) boundary has been interpreted to have resulted from a large carbon cycle disturbance during the end-Guadalupian extinction event (ca. 260 Ma). However, the carbon isotope data alone are insufficient to uniquely determine the type and magnitude of perturbation to the global carbon cycle. Calcium isotopes can be used to further constrain the cause of a carbon isotope excursion because the carbon and calcium cycles are coupled via CaCO3 burial. In this study, we present coupled carbon and calcium isotope records from three Guadalupian-Lopingian (G/L) sections in China (Penglaitan and Chaotian) and Turkey (Köserelik Tepe). The δC13 and δCa44/40 records differ among our studied sections and do not co-vary in the same manner. No section shows δC13 and δCa44/40 changes consistent with massive, rapid volcanic CO2 emissions or methane clathrate destabilization. Additionally, many sections with large (>3‰) changes in δC13 exhibit δO18 evidence for diagenetic alteration. Only one section exhibits a large excursion in the δCa44/40 of limestone but the absence of a similar excursion in the δCa44/40 of conodont apatite suggests that the limestone excursion reflects a mineralogical control rather than a perturbation to the global calcium cycle. Hence, we interpret the large isotopic changes observed in some sections to have resulted from local burial conditions or diagenetic effects, rather than from a large carbon and calcium cycle disturbance. Perturbations to the global carbon and calcium cycles across the G/L transition were much less intense than the disturbances that occurred across the subsequent Permian-Triassic boundary. This finding is consistent with the much smaller magnitude of the end-Guadalupian extinction relative to the end-Permian.

  20. GFP facilitates native purification of recombinant perlucin derivatives and delays the precipitation of calcium carbonate.

    Directory of Open Access Journals (Sweden)

    Eva Weber

    Full Text Available Insolubility is one of the possible functions of proteins involved in biomineralization, which often limits their native purification. This becomes a major problem especially when recombinant expression systems are required to obtain larger amounts. For example, the mollusc shell provides a rich source of unconventional proteins, which can interfere in manifold ways with different mineral phases and interfaces. Therefore, the relevance of such proteins for biotechnological processes is still in its infancy. Here we report a simple and reproducible purification procedure for a GFP-tagged lectin involved in biomineralization, originally isolated from mother-of-pearl in abalone shells. An optimization of E. coli host cell culture conditions was the key to obtain reasonable yields and high degrees of purity by using simple one-step affinity chromatography. We identified a dual functional role for the GFP domain when it became part of a mineralizing system in vitro. First, the GFP domain improved the solubility of an otherwise insoluble protein, in this case recombinant perlucin derivatives. Second, GFP inhibited calcium carbonate precipitation in a concentration dependent manner. This was demonstrated here using a simple bulk assay over a time period of 400 seconds. At concentrations of 2 µg/ml and higher, the inhibitory effect was observed predominantly for HCO(3 (- as the first ionic interaction partner, but not necessarily for Ca(2+. The interference of GFP-tagged perlucin derivatives with the precipitation of calcium carbonate generated different types of GFP-fluorescent composite calcite crystals. GFP-tagging offers therefore a genetically tunable tool to gently modify mechanical and optical properties of synthetic biocomposite minerals.

  1. Atmospheric deposition of organic and black carbon to the global oceans

    Science.gov (United States)

    Jurado, Elena; Dachs, Jordi; Duarte, Carlos M.; Simó, Rafel

    Atmospheric deposition of total organic carbon (OC) and black carbon (BC) is lacking or not fully accounted in most current models of the global carbon cycling, specially those fluxes related to gas phase OC. Here, we develop and apply a methodology to estimate wet and dry deposition of total OC to the oceans, based on monthly satellite measurements of aerosol size distributions, wind speed, etc., and estimates of deposition for aerosols and organic compounds. The parameterization of dry deposition velocities account for the dependence of turbulent transport with aerosol diameter, wind speed and the formation of marine aerosol, etc. Gravitational settling is estimated as a function of wet particle diameter, thus including hygroscopic growth due to ambient humidity. Global dry deposition of aerosol OC is estimated to be 11 Tg C y -1 and wet deposition of particle and gaseous OC are estimated as 47 and 187 Tg C y -1, respectively. Due to their pulsing variability, wet deposition fluxes can be important locally and as a temporal source of OC to surface waters. Dry and wet deposition of black carbon to the global ocean are estimated to be 2 and 10 Tg C yr -1, respectively, with higher fluxes in the northern hemisphere and for inter-tropical regions. Finally, considerations on the potential magnitude of the hitherto neglected gross air-sea diffusive exchange fluxes of OC are discussed. Even though the magnitude and direction of these cannot be constrained here, evidence of its important role is given. This study, thus, shows that there is an important spatial and temporal variability in atmosphere-ocean exchanges of OC and BC at different scales, and calls for the need for further research on the important role that these exchanges play in the global carbon cycle.

  2. A probabilistic assessment of calcium carbonate export and dissolution in the modern ocean

    Science.gov (United States)

    Battaglia, Gianna; Steinacher, Marco; Joos, Fortunat

    2016-05-01

    The marine cycle of calcium carbonate (CaCO3) is an important element of the carbon cycle and co-governs the distribution of carbon and alkalinity within the ocean. However, CaCO3 export fluxes and mechanisms governing CaCO3 dissolution are highly uncertain. We present an observationally constrained, probabilistic assessment of the global and regional CaCO3 budgets. Parameters governing pelagic CaCO3 export fluxes and dissolution rates are sampled using a Monte Carlo scheme to construct a 1000-member ensemble with the Bern3D ocean model. Ensemble results are constrained by comparing simulated and observation-based fields of excess dissolved calcium carbonate (TA*). The minerals calcite and aragonite are modelled explicitly and ocean-sediment fluxes are considered. For local dissolution rates, either a strong or a weak dependency on CaCO3 saturation is assumed. In addition, there is the option to have saturation-independent dissolution above the saturation horizon. The median (and 68 % confidence interval) of the constrained model ensemble for global biogenic CaCO3 export is 0.90 (0.72-1.05) Gt C yr-1, that is within the lower half of previously published estimates (0.4-1.8 Gt C yr-1). The spatial pattern of CaCO3 export is broadly consistent with earlier assessments. Export is large in the Southern Ocean, the tropical Indo-Pacific, the northern Pacific and relatively small in the Atlantic. The constrained results are robust across a range of diapycnal mixing coefficients and, thus, ocean circulation strengths. Modelled ocean circulation and transport timescales for the different set-ups were further evaluated with CFC11 and radiocarbon observations. Parameters and mechanisms governing dissolution are hardly constrained by either the TA* data or the current compilation of CaCO3 flux measurements such that model realisations with and without saturation-dependent dissolution achieve skill. We suggest applying saturation-independent dissolution rates in Earth system

  3. Preparation of carbon nanotubes with different morphology by microwave plasma enhanced chemical vapour deposition

    Energy Technology Data Exchange (ETDEWEB)

    Duraia, El-Shazly M. [Suez Canal University, Faculty of Science, Physics Department, Ismailia (Egypt); Al-Farabi Kazakh National University, 71 Al-Farabi av., 050038 Almaty (Kazakhstan); Institute of Physics and Technology, Ibragimov Street 11, 050032 Almaty (Kazakhstan); Mansurov, Zulkhair [Al-Farabi Kazakh National University, 71 Al-Farabi av., 050038 Almaty (Kazakhstan); Tokmoldin, S.Zh. [Institute of Physics and Technology, Ibragimov Street 11, 050032 Almaty (Kazakhstan)

    2010-04-15

    In this work we present a part of our results about the preparation of carbon nanotube with different morphologies by using microwave plasma enhanced chemical vapour deposition MPECVD. Well aligned, curly, carbon nanosheets, coiled carbon sheets and carbon microcoils have been prepared. We have investigated the effect of the different growth condition parameters such as the growth temperature, pressure and the hydrogen to methane flow rate ratio on the morphology of the carbon nanotubes. The results showed that there is a great dependence of the morphology of carbon nanotubes on these parameters. The yield of the carbon microcoils was high when the growth temperature was 700 C. There is a linear relation between the growth rate and the methane to hydrogen ratio. The effect of the gas pressure on the CNTs was also studied. Our samples were investigated by scanning electron microscope and Raman spectroscopy (copyright 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  4. Carbon nanofiber growth in plasma-enhanced chemical vapor deposition

    Science.gov (United States)

    Denysenko, I.; Ostrikov, K.; Cvelbar, U.; Mozetic, M.; Azarenkov, N. A.

    2008-10-01

    A theoretical model to describe the plasma-assisted growth of carbon nanofibers (CNFs) is proposed. Using the model, the plasma-related effects on the nanofiber growth parameters, such as the growth rate due to surface and bulk diffusion, the effective carbon flux to the catalyst surface, the characteristic residence time and diffusion length of carbon atoms on the catalyst surface, and the surface coverages, have been studied. The dependence of these parameters on the catalyst surface temperature and ion and etching gas fluxes to the catalyst surface is quantified. The optimum conditions under which a low-temperature plasma environment can benefit the CNF growth are formulated. These results are in good agreement with the available experimental data on CNF growth and can be used for optimizing synthesis of related nanoassemblies in low-temperature plasma-assisted nanofabrication.

  5. Change perspective to increase diagnostic accuracy of ultrasonography in calcium pyrophosphate dihydrate deposition disease! A new approach: the axial scan of the meniscus

    Directory of Open Access Journals (Sweden)

    G. Filippou

    2015-03-01

    Full Text Available Ultrasonography (US is a relevant tool in the study of calcium pyrophosphate dihydrate (CPP deposition disease. However, differential diagnosis of hyperechoic deposits within the fibrocartilage can be difficult; moreover, US study is limited by the need of an adequate acoustic window. We describe a US scanning technique that offers a new viewpoint in the study of knee meniscal structure: a longitudinal scan performed according to the long axis of meniscus. This technique proves to be particularly useful for the identification of CPP deposition, but could also improve the US diagnostic utility and accuracy in other meniscal pathologies.

  6. The prevalence of chondrocalcinosis of the symphysis pubis on CT scan and correlation with calcium pyrophosphate dihydrate crystal deposition disease.

    Science.gov (United States)

    Patel, Trusha; Ryan, Lawrence; Dubois, Melissa; Carrera, Guillermo; Baynes, Keith; Mannem, Rajeev; Mulkerin, Jennifer; Visotcky, Alexis

    2016-03-01

    Calcium pyrophosphate dihydrate (CPP) crystal deposition in the articular cartilage can often be seen radiographically as chondrocalcinosis (CC). CPP crystals preferentially deposit in fibrocartilages such as the knee menisci and symphysis pubis (SP). We sought to determine the prevalence of CC in the SP on computed tomography (CT) of the abdomen and pelvis. This retrospective study involved readings on 1070 consecutive CTs of the abdomen and pelvis performed over 3 months in patients over 65 years of age. Medical records of 226 patients found to have CC were reviewed to determine age, gender, documentation of CPPD on problem lists or in medical histories, and whether radiology readings of the CTs mentioned CC. SP CC was identified in 21.1 % (226/1070) of consecutive CT scans with the mean age of CT+ patients being 78.6. Of the 226 patients with SP CC, the observation of CC was documented in only 5.3 % (12/226) of the radiology reports. Of the 12 instances in which the radiology reports mentioned CC, this observation was never (0/12) transmitted to the medical history or problem list. The prevalence of SP CC in patients older than 65 was 21.1 %. Since the majority of CTs of the abdomen and pelvis are not ordered for evaluation of musculoskeletal conditions, this is likely a true prevalence without selection bias. When CC of the SP was present on images, radiologists routinely overlooked or chose not to report CC. Even in the rare instances when it was reported, that information was not added to the medical history or problem list. There are several clinical situations (e.g., acute monoarthritis or atypical osteoarthritis) in which recognizing that a patient has CPP deposition would be useful. Taking the time to review images may yield clinically important findings that are not mentioned anywhere on the patient chart.

  7. Interlaminar improvement of carbon fiber/epoxy composites via depositing mixture of carbon nanotubes and sizing agent

    Science.gov (United States)

    Fang, Cuiqin; Wang, Julin; Zhang, Tao

    2014-12-01

    The effects of deposition to carbon fibers surfaces with mixture of functionalized multi-walled carbon fibers (MWCNTs) and sizing agent were investigated. Relationships between CNTs and sizing agent were studied with Fourier transform infrared spectrometer (FTIR), X-ray photoelectron spectroscopy (XPS) and Ubbelohde viscometer. The results revealed that CNTs could react with sizing agent at 120 °C, and optimal reaction occurs when mass ratio was about 1:20. Then, carbon fibers were immersed in mixed aqueous suspension of CNTs and sizing agent with the above ratio dispersed by ultrasonication. According to scanning electron microscope (SEM) observations, fibers surfaces were coated with CNTs and sizing agent. The static contact angle tests indicated wetting performance between fibers and epoxy resin were improved after deposited procedures. Interlaminar shear strength was increased by 67.01% for fibers/epoxy resin composites after mixture deposited process. Moreover, the tensile strength of single fibers after depositing showed a slightly increase compared with that of fibers without depositing layer.

  8. A Model-Based Analysis of Nitrogen Deposition: Effects on Forest Carbon Sequestration

    Science.gov (United States)

    Dezi, S.; Medlyn, B. E.; Tonon, G.; Magnani, F.

    2009-04-01

    Over the last 150 years nitrogen deposition has increased, especially in the northern hemisphere, mainly due to the use of fossil fuels, deforestation and agricultural practices. Although the impact of this increase on the terrestrial carbon cycle is still uncertain, it is likely that this large perturbation of the global nitrogen cycle will have important effects on carbon cycling, particularly via impacts on forest carbon storage. In the present work we investigated qualitatively the overall response of forest carbon sequestration to nitrogen deposition, and the relative importance of different mechanisms that bring about this response. For this purpose we used the G'DAY forest carbon-nitrogen cycling model (Comins and McMurtrie 1993), introducing some new assumptions which focus on the effect of nitrogen deposition. Specifically the new assumptions are: (i) foliar litterfall and specific leaf area (SLA) are functions of leaf nitrogen concentration; (ii) belowground C allocation is a function of net primary production (NPP); (iii) forest canopies can directly take up nitrogen; (iv) management of forests occurs; (v) leaching occurs only for nitrate nitrogen. We investigated the effect of each assumption on net ecosystem production (NEP), with a step increase in nitrogen deposition from a steady state of 0.4 gN m-2 yr-1 to 2 gN m-2 yr-1, and then running the old and new model versions for different nitrogen deposition levels. Our analysis showed that nitrogen deposition can have a large effect on forest carbon storage at ecosystem level. In particular the effect of the assumptions (ii), (iii) and (iv) seem to be of greater importance, giving rise to a markedly higher level of forest carbon sequestration than in their absence. On the contrary assumptions (i) and (v) seem not to have any particular effect on the NEP simulated. Finally, running the models for different levels of nitrogen deposition showed that estimating forest carbon exchange without taking into

  9. Electrophoretic Deposition of Carbon Nanotubes on 3-Amino-Propyl-Triethoxysilane (APTES Surface Functionalized Silicon Substrates

    Directory of Open Access Journals (Sweden)

    Theda Daniels-Race

    2013-05-01

    Full Text Available Fabrication of uniform thin coatings of multi-walled carbon nanotubes (MWCNTs by electrophoretic deposition (EPD on semiconductor (silicon substrates with 3-aminopropyl-triethoxysilane (APTES surface functionalization has been studied extensively in this report. The gradual deposition and eventual film formation of the carbon nanotubes (CNTs is greatly assisted by the Coulombic force of attraction existing between the positively charged –NH2 surface groups of APTES and the acid treated, negatively charged nanotubes migrating towards the deposition surfaces. The remarkable deposition characteristics of the CNT coatings by EPD in comparison to the dip coating method and the influence of isopropyl (IPA-based CNT suspension in the fabricated film quality has also been revealed in this study. The effect of varying APTES concentration (5%–100% on the Raman spectroscopy and thickness of the deposited CNT film has been discussed in details, as well. The deposition approach has eliminated the need of metal deposition in the electrophoretic deposition approach and, therefore, establishes a cost-effective, fast and entirely room temperature-based fabrication strategy of CNT thin films for a wide range of next generation electronic applications.

  10. Influence of bias on properties of carbon films deposited by MCECR plasma sputtering method

    Institute of Scientific and Technical Information of China (English)

    CAI Chang-long; DIAO Dong-feng; S.Miyake; T.Matsumoto

    2004-01-01

    The mirror-confinement-type electron cyclotron resonance(MCECR) plasma source has high plasma density and high electron temperature. It is quite useful in many plasma processing, and has been used for etching and thin-film deposition. The carbon films with 40 nm thickness were deposited by MCECR plasma sputtering method on Si, and the influence of substrate bias on the properties of carbon films was studied. The bonding structure of the film was analyzed by the X-ray photoelectron spectroscopy(XPS), the tribological properties were measured by the pin-on-disk(POD) tribometer, the nanohardness of the films was measured by the nanoindenter, and the deposition speed and the refractive index were measured by the ellipse meter. The better substrate bias was obtained, and the better properties of carbon films were obtained.

  11. Nanocomposite tantalum-carbon-based films deposited by femtosecond pulsed laser ablation

    Energy Technology Data Exchange (ETDEWEB)

    Benchikh, N. [Laboratoire Traitement du Signal et Instrumentation, UMR 5516, Universite J. Monnet, 10 rue Barrouin, 42000 Saint-Etienne (France); Garrelie, F. [Laboratoire Traitement du Signal et Instrumentation, UMR 5516, Universite J. Monnet, 10 rue Barrouin, 42000 Saint-Etienne (France); Wolski, K. [Ecole Nationale Superieure des Mines de Saint-Etienne, Centre SMS - URA CNRS 5146, 158 cours Fauriel, 42023 Saint-Etienne, Cedex 02 (France); Donnet, C. [Laboratoire Traitement du Signal et Instrumentation, UMR 5516, Universite J. Monnet, 10 rue Barrouin, 42000 Saint-Etienne (France)]. E-mail: Christophe.Donnet@univ-st-etienne.fr; Fillit, R.Y. [Ecole Nationale Superieure des Mines de Saint-Etienne, Centre SMS - URA CNRS 5146, 158 cours Fauriel, 42023 Saint-Etienne, Cedex 02 (France); Rogemond, F. [Laboratoire Traitement du Signal et Instrumentation, UMR 5516, Universite J. Monnet, 10 rue Barrouin, 42000 Saint-Etienne (France); Subtil, J.L. [Laboratoire Traitement du Signal et Instrumentation, UMR 5516, Universite J. Monnet, 10 rue Barrouin, 42000 Saint-Etienne (France); Rouzaud, J.N. [Laboratoire de Geologie de l' Ecole Normale Superieure de Paris 24, rue Lhomond 75231-Paris Cedex 5 (France); Laval, J.Y. [Laboratoire de Physique du Solide, UPR5 CNRS-ESPCI, 10 rue Vauquelin 75231-Paris Cedex 05 (France)

    2006-01-03

    Nanostructured coatings of metal (tantalum) containing diamond-like carbon (a-C:Ta) have been prepared by femtosecond pulsed laser deposition (PLD). The films, containing 15 at.% tantalum, have been deposited by ablating sequentially graphite and metallic tantalum in vacuum conditions with an amplified Ti:sapphire laser. The coatings have been investigated by X-ray photoelectron spectroscopy, grazing angle X-ray diffraction, energy filtered transmission electron microscopy, scanning and high resolution transmission electron microscopies. Evidence of metallic {alpha}-Ta and {beta}-Ta particles (diameter in the 100 nm range) and smaller quasi-amorphous tantalum clusters embedded in the carbonaceous matrix have been shown. A thin tantalum carbide interface between the carbon matrix and the top surface of the tantalum nodules has also been identified. The ability of femtosecond pulsed laser deposition to synthetize nanocomposite carbon-based films and to control their nanostructure is discussed.

  12. Depositing nanometer-sized particles of metals onto carbon allotropes

    Science.gov (United States)

    Watson, Kent A. (Inventor); Fallbach, Michael J. (Inventor); Ghose, Sayata (Inventor); Smith, Joseph G. (Inventor); Delozier, Donavon M. (Inventor); Connell, John W. (Inventor)

    2010-01-01

    A process for depositing nanometer-sized metal particles onto a substrate in the absence of aqueous solvents, organic solvents, and reducing agents, and without any required pre-treatment of the substrate, includes preparing an admixture of a metal compound and a substrate by dry mixing a chosen amount of the metal compound with a chosen amount of the substrate; and supplying energy to the admixture in an amount sufficient to deposit zero valance metal particles onto the substrate. This process gives rise to a number of deposited metallic particle sizes which may be controlled. The compositions prepared by this process are used to produce polymer composites by combining them with readily available commodity and engineering plastics. The polymer composites are used as coatings, or they are used to fabricate articles, such as free-standing films, fibers, fabrics, foams, molded and laminated articles, tubes, adhesives, and fiber reinforced articles. These articles are well-suited for many applications requiring thermal conductivity, electrical conductivity, antibacterial activity, catalytic activity, and combinations thereof.

  13. Nanostructured Diamond-Like Carbon Films Grown by Off-Axis Pulsed Laser Deposition

    Directory of Open Access Journals (Sweden)

    Seong Shan Yap

    2015-01-01

    Full Text Available Nanostructured diamond-like carbon (DLC films instead of the ultrasmooth film were obtained by pulsed laser ablation of pyrolytic graphite. Deposition was performed at room temperature in vacuum with substrates placed at off-axis position. The configuration utilized high density plasma plume arriving at low effective angle for the formation of nanostructured DLC. Nanostructures with maximum size of 50 nm were deposited as compared to the ultrasmooth DLC films obtained in a conventional deposition. The Raman spectra of the films confirmed that the films were diamond-like/amorphous in nature. Although grown at an angle, ion energy of >35 eV was obtained at the off-axis position. This was proposed to be responsible for subplantation growth of sp3 hybridized carbon. The condensation of energetic clusters and oblique angle deposition correspondingly gave rise to the formation of nanostructured DLC in this study.

  14. Atmospheric nitrogen deposition promotes carbon loss from peat bogs

    NARCIS (Netherlands)

    Bragazza, L.; Freeman, C.; Jones, T.; Rydin, H.; Limpens, J.; Fenner, N.; Ellis, T.; Gerdol, R.; Hajek, M.; Hajek, T.; Iacumin, P.; Kutnar, L.; Tahvanainen, T.; Toberman, H.

    2006-01-01

    Peat bogs have historically represented exceptional carbon (C) sinks because of their extremely low decomposition rates and consequent accumulation of plant remnants as peat. Among the factors favoring that peat accumulation, a major role is played by the chemical quality of plant litter itself, whi

  15. Pyrolytic deposition of nanostructured titanium carbide coatings on the surface of multiwalled carbon nanotubes

    Science.gov (United States)

    Kremlev, K. V.; Ob"edkov, A. M.; Ketkov, S. Yu.; Kaverin, B. S.; Semenov, N. M.; Gusev, S. A.; Tatarskii, D. A.; Yunin, P. A.

    2016-05-01

    Nanostructured titanium carbide coatings have been deposited on the surface of multiwalled carbon nanotubes (MWCNTs) by the MOCVD method with bis(cyclopentadienyl)titanium dichloride precursor. The obtained TiC/MWCNT hybrid materials were characterized by X-ray diffraction, scanning electron microscopy, and high-resolution transmission electron microscopy. It is established that a TiC coating deposits onto the MWCNT surface with the formation of a core-shell (MWSNT-TiC) type structure.

  16. Functionalization and Area-Selective Deposition of Magnetic Carbon-Coated Iron Nanoparticles from Solution

    Directory of Open Access Journals (Sweden)

    Erika Widenkvist

    2011-01-01

    Full Text Available A route to area-selective deposition of carbon-coated iron nanoparticles, involving chemical modification of the surface of the particles, is described. Partial oxidative etching of the coating introduces carboxylic groups, which then are esterified. The functionalized particles can be selectively deposited on the Si areas of Si/SiO2 substrates by a simple dipping procedure. Nanoparticles and nanoassemblies have been analyzed using SEM, TEM, and XPS.

  17. The Study of Thermal Decomposition of Natural Calcium Carbonate by the Temperature-programmed Mass Spectrometry Technique

    OpenAIRE

    S.N. Danilchenko; V.D. Chіvanov; A.G. Ryabishev; S.V. Novіkov; A.A. Stepanenko; V.N. Kuznetsov; E.V. Mironets; A.V. Marіychuk; A.A. Yanovska; O.G. Bordunova; A.N. Bugay

    2016-01-01

    The experiments have shown that the heating range for quantitative evolution of carbon dioxide gas (CO2) from natural calcium carbonates (e.g., chalk, corals, shells of the Anadara clams (Anadara inaequivalvis), shell of bird eggs) is from 500 to 850 C with a total heating time of 30-50 minutes. The only exception is the sample of a mortar from a masonry of Saint Sophia Cathedral (the architectural monument of XI century), in which the lowest border of the heating range for carbon dioxide ev...

  18. Pore-size-dependent calcium carbonate precipitation controlled by surface chemistry.

    Science.gov (United States)

    Stack, Andrew G; Fernandez-Martinez, Alejandro; Allard, Lawrence F; Bañuelos, José L; Rother, Gernot; Anovitz, Lawrence M; Cole, David R; Waychunas, Glenn A

    2014-06-03

    Induced mineral precipitation is potentially important for the remediation of contaminants, such as during mineral trapping during carbon or toxic metal sequestration. The prediction of precipitation reactions is complicated by the porous nature of rocks and soils and their interaction with the precipitate, introducing transport and confinement effects. Here X-ray scattering measurements, modeling, and electron microscopies were used to measure the kinetics of calcium carbonate precipitation in a porous amorphous silica (CPG) that contained two discrete distributions of pore sizes: nanopores and macropores. To examine the role of the favorability of interaction between the substrate and precipitate, some of the CPG was functionalized with a self-assembled monolayer (SAM) similar to those known to enhance nucleation densities on planar substrates. Precipitation was found to occur exclusively in macropores in the native CPG, while simultaneous precipitation in nanopores and macropores was observed in the functionalized CPG. The rate of precipitation in the nanopores estimated from the model of the X-ray scattering matched that measured on calcite single crystals. These results suggest that the pore-size distribution in which a precipitation reaction preferentially occurs depends on the favorability of interaction between substrate and precipitate, something not considered in most studies of precipitation in porous media.

  19. Influences of iron and calcium carbonate on wastewater treatment performances of algae based reactors.

    Science.gov (United States)

    Zhao, Zhimiao; Song, Xinshan; Wang, Wei; Xiao, Yanping; Gong, Zhijie; Wang, Yuhui; Zhao, Yufeng; Chen, Yu; Mei, Mengyuan

    2016-09-01

    The influences of iron and calcium carbonate (CaCO3) addition in wastewater treatments reactors performance were investigated. Adding different concentrations of Fe(3+) (5, 10, 30 and 50mmol/m(3)), iron and CaCO3 powder led to changes in algal characteristics and physico-chemical and microbiological properties. According to the investigation results, nutrient removal efficiency in algae based reactors was obviously increased by the addition of 10mmol/m(3) Fe(3+), iron (5mmol/m(3)) and CaCO3 powder (0.2gm(-3)) and the removal efficiencies of BOD5, TN, and TP in Stage 2 were respectively increased by 28%, 8.9%, and 22%. The improvements in physico-chemical performances were verified by microbial community tests (bacteria quantity, activity and community measured in most probable number, extracellular enzymes activity, and Biolog Eco Plates). Microbial variations indicated the coexistence of Fe ions and carbonate-bicarbonate, which triggered the synergistic effect of physico-chemical action and microbial factors in algae based reactors.

  20. Mechanochemically Activated, Calcium Oxide-Based, Magnesium Oxide-Stabilized Carbon Dioxide Sorbents.

    Science.gov (United States)

    Kurlov, Alexey; Broda, Marcin; Hosseini, Davood; Mitchell, Sharon J; Pérez-Ramírez, Javier; Müller, Christoph R

    2016-09-01

    Carbon dioxide capture and storage (CCS) is a promising approach to reduce anthropogenic CO2 emissions and mitigate climate change. However, the costs associated with the capture of CO2 using the currently available technology, that is, amine scrubbing, are considered prohibitive. In this context, the so-called calcium looping process, which relies on the reversible carbonation of CaO, is an attractive alternative. The main disadvantage of naturally occurring CaO-based CO2 sorbents, such as limestone, is their rapid deactivation caused by thermal sintering. Here, we report a scalable route based on wet mechanochemical activation to prepare MgO-stabilized, CaO-based CO2 sorbents. We optimized the synthesis conditions through a fundamental understanding of the underlying stabilization mechanism, and the quantity of MgO required to stabilize CaO could be reduced to as little as 15 wt %. This allowed the preparation of CO2 sorbents that exceed the CO2 uptake of the reference limestone by 200 %.

  1. Atomistic simulations of calcium uranyl(VI) carbonate adsorption on calcite and stepped-calcite surfaces.

    Science.gov (United States)

    Doudou, Slimane; Vaughan, David J; Livens, Francis R; Burton, Neil A

    2012-07-17

    Adsorption of actinyl ions onto mineral surfaces is one of the main mechanisms that control the migration of these ions in environmental systems. Here, we present computational classical molecular dynamics (MD) simulations to investigate the behavior of U(VI) in contact with different calcite surfaces. The calcium-uranyl-carbonate [Ca(2)UO(2)(CO(3))(3)] species is shown to display both inner- and outer-sphere adsorption to the flat {101̅4} and the stepped {314̅8} and {31̅2̅16} planes of calcite. Free energy calculations, using the umbrella sampling method, are employed to simulate adsorption paths of the same uranyl species on the different calcite surfaces under aqueous condition. Outer-sphere adsorption is found to dominate over inner-sphere adsorption because of the high free energy barrier of removing a uranyl-carbonate interaction and replacing it with a new uranyl-surface interaction. An important binding mode is proposed involving a single vicinal water monolayer between the surface and the sorbed complex. From the free energy profiles of the different calcite surfaces, the uranyl complex was also found to adsorb preferentially on the acute-stepped {314̅8} face of calcite, in agreement with experiment.

  2. Synthesis of nanostructured carbon by chlorination of calcium carbide at moderate temperatures and its performance evaluation

    Energy Technology Data Exchange (ETDEWEB)

    Dai Chunling [School of Chemistry, Xiangtan University, Hunan 411105 (China); Wang, Xianyou [School of Chemistry, Xiangtan University, Hunan 411105 (China)], E-mail: wxianyou@yahoo.com; Wang Ying [School of Chemical Engineering and Pharmacy, Wuhan Institute of Technology, Hubei 430073 (China); Li Na; Wei Jianliang [School of Chemistry, Xiangtan University, Hunan 411105 (China)

    2008-12-01

    A new type of one-step preparation technique for the calcium carbide-derived carbon (CaC{sub 2}-CDC) was developed. In this study, CaC{sub 2}-CDC was synthesized from CaC{sub 2} in a freshly prepared chlorine environment in the temperature range of 100-600 deg. C. The structure and morphology of as-prepared CaC{sub 2}-CDC were studied by X-ray diffraction, transmission electron microscopy and nitrogen sorption experiment. Analysis of X-ray diffraction and transmission electron microscopy showed that CaC{sub 2}-CDC is an amorphous nanoporous material, and the structure depended on the synthesis temperature. The resultant carbon demonstrated narrow pore size distribution (PSD) and specific surface area (SSA) close to 800 m{sup 2} g{sup -1} (for nitrogen sorption) at a synthesized temperature of 100 deg. C. Increasing the reaction temperature above 400 deg. C resulted in a lower SSA of CaC{sub 2}-CDC due to the beginning of graphitization tendency. The nanoporous structure and narrow PSD of CaC{sub 2}-CDC indicated potential application as electrode materials in supercapacitor. The CaC{sub 2}-CDC exhibited a specific capacitance of 127.7 F g{sup -1} measured from the three-electrode cyclic voltammetry experiment at 10 mV s{sup -1}.

  3. Carbonate replacement of lacustrine gypsum deposits in two Neogene continental basins, eastern Spain

    Science.gov (United States)

    Anadón, P.; Rosell, L.; Talbot, M. R.

    1992-07-01

    Bedded nonmarine gypsum deposits in the Miocene Teruel and Cabriel basins, eastern Spain, are partly replaced by carbonate. The Libros gypsum (Teruel Graben) is associated with fossiliferous carbonate wackestones and finely laminated, organic matter-rich mudstones which accumulated under anoxic conditions in a meromictic, permanent lake. The gypsum is locally pseudomorphed by aragonite or, less commonly, replaced by calcite. Low δ 13C values indicate that sulphate replacement resulted from bacterial sulphate reduction processes that were favoured by anacrobic conditions and abundant labile organic matter in the sediments. Petrographic evidence and oxygen isotopic composition suggest that gypsum replacement by aragonite occurred soon after deposition. A subsequent return to oxidising conditions caused some aragonite to be replaced by diagenetic gypsum. Native sulphur is associated with some of these secondary gypsum occurrences. The Los Ruices sulphate deposits (Cabriel Basin) contain beds of clastic and selenitic gypsum which are associated with limestones and red beds indicating accumulation in a shallow lake. Calcite is the principal replacement mineral. Bacterial sulphate reduction was insignificant in this basin because of a scarcity of organic matter. Stable isotope composition of diagenetic carbonate indicates that gypsum replacement occurred at shallow burial depths due to contact with dilute groundwaters of meteoric origin. Depositional environment evidently has a major influence upon the diagenetic history of primary sulphate deposits. The quantity of preserved organic matter degradable by sulphate-reducing bacteria is of particular importance and, along with groundwater composition, is the main factor controlling the mechanism of gypsum replacement by carbonate.

  4. Adsorption efficiencies of calcium (II ion and iron (II ion on activated carbon obtained from pericarp of rubber fruit

    Directory of Open Access Journals (Sweden)

    Orawan Sirichote

    2008-03-01

    Full Text Available Determination of adsorption efficiencies of activated carbon from pericarp of rubber fruit for calcium (II ion and iron (II ion has been performed by flowing the solutions of these ions through a column of activated carbon. The weights of activated carbon in 500 mL buret column (diameter 3.2 cm for flowing calcium (II ion and iron (II ion solutions were 15 g and 10 g, respectively. The initial concentration of calcium ion was prepared to be about eight times more diluted than the true concentration found in the groundwater from the lower part of southern Thailand. Calcium (II ion concentrations were analysed by EDTA titration and its initial concentration was found to be 23.55 ppm. With a flow rate of 26 mL/min, the adsorption efficiency was 11.4 % with passed through volume 4.75 L. Iron (II ion concentrations were analysed by spectrophotometric method; its initial concentration was found to be 1.5565 ppm. At a flow rate of 22 mL/min, the adsorption efficiency was 0.42 % with passed through volume of 34.0 L.

  5. Ironstone deposits hosted in Eocene carbonates from Bahariya (Egypt)-New perspective on cherty ironstone occurrences

    Science.gov (United States)

    Afify, A. M.; Sanz-Montero, M. E.; Calvo, J. P.

    2015-11-01

    This paper gives new insight into the genesis of cherty ironstone deposits. The research was centered on well-exposed, unique cherty ironstone mineralization associated with Eocene carbonates from the northern part of the Bahariya Depression (Egypt). The economically important ironstones occur in the Naqb Formation (Early Eocene), which is mainly formed of shallow marine carbonate deposits. Periods of lowstand sea-level caused extensive early dissolution (karstification) of the depositional carbonates and dolomitization associated with mixing zones of fresh and marine pore-water. In faulted areas, the Eocene carbonate deposits were transformed into cherty ironstone with preservation of the precursor carbonate sedimentary features, i.e. skeletal and non-skeletal grain types, thickness, bedding, lateral and vertical sequential arrangement, and karst profiles. The ore deposits are composed of iron oxyhydroxides, mainly hematite and goethite, chert in the form of micro- to macro-quartz and chalcedony, various manganese minerals, barite, and a number of subordinate sulfate and clay minerals. Detailed petrographic analysis shows that quartz and iron oxides were coetaneous and selectively replaced carbonates, the coarse dolomite crystals having been preferentially transformed into quartz whereas the micro-crystalline carbonates were replaced by the iron oxyhydroxides. A number of petrographic, sedimentological and structural features including the presence of hydrothermal-mediated minerals (e.g., jacobsite), the geochemistry of the ore minerals as well as the structure-controlled location of the mineralization suggest a hydrothermal source for the ore-bearing fluids circulating through major faults and reflect their proximity to centers of magmatism. The proposed formation model can contribute to better understanding of the genetic mechanisms of formation of banded iron formations (BIFs) that were abundant during the Precambrian.

  6. Growth of the calcium carbonate polymorph vaterite in mixtures of water and ethylene glycol at conditions of gas processing

    Science.gov (United States)

    Flaten, Ellen Marie; Seiersten, Marion; Andreassen, Jens-Petter

    2010-03-01

    Long subsea tie-ins for transportation of moist gas and condensate require corrosion and hydrate control. The combination of alkalinity for corrosion mitigation and monoethylene glycol (MEG) for hydrate inhibition strongly affects the tolerance for produced formation water. The elevated alkalinity downstream of the injection point increases the risk of carbonate formation. Calcium carbonate is the most common precipitate at such conditions. Our previous findings (Flaten et al., 2009) [1] show that MEG governs calcium carbonate precipitation and promotes formation of the metastable polymorph vaterite. This paper describes crystal growth of vaterite in mixed MEG water solvent with 0-70 wt% MEG at temperatures of 40 and 70 °C in solutions with high calcium to carbonate ratios representative of the production conditions. Results of some experiments in solutions with stoichiometric amounts of the reactants are included for comparison. The growth rate of vaterite can be described by second-order kinetics in most of the investigated supersaturation range. The growth order is lower at high MEG contents and high calcium concentrations when the carbonate activity is reduced in order to maintain comparable supersaturation values. It is then probable that the low carbonate activity makes the reaction diffusion limited. MEG reduces the growth rate constant of vaterite when the reaction is second order. Increasing the MEG concentration from 0 to 50 wt%, decreases the growth rate constant kr from 1.9 to 0.7 nm/s at 40 °C and from 2.6 to 1.2 nm/s at 70 °C. The growth reduction can be explained by a change of either de-hydration or diffusion rate along the surface when the ions are incorporated into the crystal lattice. Further investigations into which of the two mechanisms that is rate determining is outside the scope of this work.

  7. Preparation and characterization of boron nitride coatings on carbon fibers from borazine by chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    Li Junsheng, E-mail: charlesljs@163.com [State Key Laboratory of Advanced Ceramic Fibers and Composites, College of Aerospace and Materials Engineering, National University of Defense Technology, Changsha, 410073 (China); Zhang Changrui; Li Bin [State Key Laboratory of Advanced Ceramic Fibers and Composites, College of Aerospace and Materials Engineering, National University of Defense Technology, Changsha, 410073 (China)

    2011-06-15

    Boron nitride (BN) coatings were deposited on carbon fibers by chemical vapor deposition (CVD) using borazine as single source precursor. The deposited coatings were characterized by scanning electron microscopy (SEM), Auger electron spectroscopy (AES), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy. The effect of temperatures on growth kinetics, morphology, composition and structure of the coatings was investigated. In the low temperature range of 900 deg. C-1000 deg. C, the growth rate increased with increasing temperature complying with Arrhenius law, and an apparent active energy of 72 kJ/mol was calculated. The coating surface was smooth and compact, and the coatings uniformly deposited on individual fibers of carbon fiber bundles. The growth was controlled by surface reaction. At 1000 deg. C, the deposition rate reached a maximum (2.5 {mu}m/h). At the same time, the limiting step of the growth translated to be mass-transportation. Above 1100 deg. C, the growth rate decreased drastically due to the occurrence of gas-phase nucleation. Moreover, the coating surface became loose and rough. Composition and structure examinations revealed that stoichiometric BN coatings with turbostratic structure were obtained below 1000 deg. C, while hexagonal BN coatings were deposited above 1100 deg. C. A penetration of carbon element from the fibers to the coatings was observed.

  8. The formation of web-like connection among electrospun chitosan/PVA fiber network by the reinforcement of ellipsoidal calcium carbonate.

    Science.gov (United States)

    Sambudi, Nonni Soraya; Kim, Minjeong G; Park, Seung Bin

    2016-03-01

    The electrospun fibers consist of backbone fibers and nano-branch network are synthesized by loading of ellipsoidal calcium carbonate in the mixture of chitosan/poly(vinyl alcohol) (PVA) followed by electrospinning. The synthesized ellipsoidal calcium carbonate is in submicron size (730.7±152.4 nm for long axis and 212.6±51.3 nm for short axis). The electrospun backbone fibers experience an increasing in diameter by loading of calcium carbonate from 71.5±23.4 nm to 281.9±51.2 nm. The diameters of branch fibers in the web-network range from 15 nm to 65 nm with most distributions of fibers are in 30-35 nm. Calcium carbonate acts as reinforcing agent to improve the mechanical properties of fibers. The optimum value of Young's modulus is found at the incorporation of 3 wt.% of calcium carbonate in chitosan/PVA fibers, which is enhanced from 15.7±3 MPa to 432.4±94.3 MPa. On the other hand, the ultimate stress of fibers experiences a decrease. This result shows that the fiber network undergoes changes from flexible to more stiff by the inclusion of calcium carbonate. The thermal analysis results show that the crystallinity of polymer is changed by the existence of calcium carbonate in the fiber network. The immersion of fibers in simulated body fluid (SBF) results in the formation of apatite on the surface of fibers.

  9. Bamboo and herringbone shaped carbon nanotubes and carbon nanofibres synthesized in direct current-plasma enhanced chemical vapour deposition.

    Science.gov (United States)

    Zhang, Lu; Chen, Li; Wells, Torquil; El-Gomati, Mohamed

    2009-07-01

    Carbon nanotubes with different structures were catalytically synthesized on Ni coated SiO2/Si substrate in a Direct Current Plasma Enhanced Chemical Vapour Deposition system, in which C2H2 acted as the carbon source and NH3 as the etchant gas. A Scanning Electron Microscope study showed that carbon nanotubes were all vertically aligned with respect to the substrate, with diameters ranging from 10 nm to 200 nm. Different sizes of Ni catalyst particles were observed on the tips of carbon nanotubes. Transmission Electron Microscopy was used to study the morphology of the grown tubes and the results obtained show that the diameters and structures of these carbon nanotubes were closely correlated to the sizes and structures of the Ni nanoparticles. Two main structures namely bamboo shaped carbon nanotubes and herringbone shaped carbon nanofibres were found on the same sample. It is suggested that by controlling the pre-growth condition, desired structure of carbon nanotubes or carbon nanofibres could be produced for practical applications.

  10. Composition and Microstructure of Magnetron Sputtering Deposited Ti-containing Amorphous Carbon Films

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Ti-containing carbon films were deposited by using magnetron sputtering deposition. The composition and microstructure of the carbon films were characterized in detail by combining the techniques of Rutherford backscattering spectrometry (RBS), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and transmission electron microscopy (TEM). It is found that carbon films contain Ti 18 at pct; after Ti incorporation, the films consist of titanium carbide; C1s peak appears at 283.4 eV and it could be divided into 283.29 and 284.55 eV, representing sp2 and sp3, respectively, and sp2 is superior to sp3. This Ti-containing film with dominating sp2 bonds is nanocomposites with nanocrystalline TiC clusters embedded in an amorphous carbon matrix, which could be proved by XRD and TEM.

  11. Deposition of carbon nitride films for space application

    Institute of Scientific and Technical Information of China (English)

    Feng Yu-Dong; Xu Chao; Wang Yi; Zhang Fu-Jia

    2006-01-01

    Carbon nitride thin films were prepared by electron-beam evaporation assisted with nitrogen ion bombardment and TiN/CNx composite films were by unbalanced dc magnetron sputtering, respectively. It was found that the sputtered films were better than the evaporated films in hardness and adhesion. The experiments of atomic oxygen action, cold welding, friction and wearing were emphasized, and the results proved that the sputtered TiN/CNx composite films were suitable for space application.

  12. Influence of dc bias on amorphous carbon deposited by pulse laser ablation

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Amorphous carbon films were deposited on single-crystalline silicon and K9 glass by pulse laser ablation using different negative substrate bias. Scanning electron microscope (SEM) was used to observe morphology of the surface. Thickness and refractive index of the film deposited on K9 glass were measured by ellipsometry. Micro-hardness of films was measured relatively to single crystal silicon. All films deposited on silicon were analyzed by Raman spectra. All spectra were deconvoluted to three peaks. Line-width ratios varied similarly with bias voltage when the laser energy was kept invariant.

  13. Microwave plasma-enhanced chemical vapour deposition growth of carbon nanostructures

    Directory of Open Access Journals (Sweden)

    Shivan R. Singh

    2010-05-01

    Full Text Available The effect of various input parameters on the production of carbon nanostructures using a simple microwave plasma-enhanced chemical vapour deposition technique has been investigated. The technique utilises a conventional microwave oven as the microwave energy source. The developed apparatus is inexpensive and easy to install and is suitable for use as a carbon nanostructure source for potential laboratory-based research of the bulk properties of carbon nanostructures. A result of this investigation is the reproducibility of specific nanostructures with the variation of input parameters, such as carbon-containing precursor and support gas flow rate. It was shown that the yield and quality of the carbon products is directly controlled by input parameters. Transmission electron microscopy and scanning electron microscopy were used to analyse the carbon products; these were found to be amorphous, nanotubes and onion-like nanostructures.

  14. Theoretical Descriptions of Carbon Nanotubes Synthesis in a Chemical Vapor Deposition Reactor: A Review

    OpenAIRE

    Lubej, M.; Plazl, I.

    2012-01-01

    The mechanisms by which carbon nanotubes nucleate and grow are still poorly understood. Understanding and mathematically describing the process is crucial for its optimization. This paper reviews different models which have been proposed to explain carbon nanotube growth in the chemical vapor deposition process. The review is divided into two sections, the first section describes some nucleation, growth and termination simulations based on molecular dynamics, and the second section describes ...

  15. Purification of Single-walled Carbon Nanotubes Grown by a Chemical Vapour Deposition (CVD) Method

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A procedure for purification of single-walled carbon nanotubes(SWNTs) grown by the chemical vapour deposition (CVD) of carbon monooxide has been developed. Based on the result from TGA/DTA of as-prepared sample, the oxidation temperature was determined. The process included sonication, oxidation and acid washing steps. The purity and yield after purification were determined and estimated by TEM. Moreover, for the first time, a loop structure for CVD SWNTs has been observed.

  16. Impact of sodium polyacrylate on the amorphous calcium carbonate formation from supersaturated solution.

    Science.gov (United States)

    Liu, J; Pancera, S; Boyko, V; Gummel, J; Nayuk, R; Huber, K

    2012-02-21

    A detailed in situ scattering study has been carried out on the formation of amorphous calcium carbonate (ACC) particles modulated by the presence of small amounts of sodium polyacrylate chains. The work is aiming at an insight into the modulation of ACC formation by means of two polyacrylate samples differing in their molecular weight by a factor of 50. The ACC formation process was initiated by an in situ generation of CO(3)(2-) ions via hydrolysis of 10 mM dimethylcarbonate in the presence of 10 mM CaCl(2). Analysis of the formation process by means of time-resolved small-angle X-ray and light scattering in the absence of any additives provided evidence for a monomer addition mechanism for the growth of ACC particles. ACC formation under these conditions sets in after a lag-period of some 350 s. In the presence of sodium polyacrylate chains, calcium polyacrylate aggregates are formed during the lag-period, succeeded by a modulated ACC growth in a second step. The presence of anionic polyacrylate chains changed the shape of the growing particles toward loose and less homogeneous entities. In the case of low amounts (1.5-7.5 mg/L) of the long chain additive with 97 kDa, the size of the aggregates is comparable to the size of the successively formed hybrid particles. No variation of the lag-period has been observed in this case. Use of the short chain additive with 2 kDa enabled increase of the additive concentration up to 100 mg/L and resulted in a significant increase of the lag-period. This fact, together with the finding that the resulting hybrid particles remained stable in the latter case, identified short chain sodium polyacrylates as more efficient modulators than long chain polyacrylates.

  17. Carbon film deposition from high velocity rarefied flow

    Energy Technology Data Exchange (ETDEWEB)

    Rebrov, A.K., E-mail: rebrov@itp.nsc.ru; Emelyanov, A.A.; Yudin, I.B.

    2015-01-30

    The presented study is based on the idea of the activation of a gas-precursor high velocity flow by hot wire. The wire forms the channel for flow before expansion to substrate. The construction allows change of the specific flow rate, velocity, composition and temperature of a gas mixture by studying the film synthesis in conditions from free molecular to continuum flow at velocities from hundreds to thousands of m/s. At a high pressure, the film has typical and unusual hexagonal incorporations for diamond tetragonal particles. Raman spectrum with the pronounced diamond peak is typical for diamond-like film. X-ray diffraction points in the presence of lonsdaleite. Conditions of deposition were simulated by Monte Carlo method. Collisions with hot surfaces and chemical transformations were taken into consideration as well.

  18. Photoinduced crystallization of calcium carbonate from a homogeneous precursor solution in the presence of partially hydrolyzed poly(vinyl alcohol)

    Science.gov (United States)

    Nishio, Takashi; Naka, Kensuke

    2015-04-01

    Photoinduced crystallization of calcium carbonate (CaCO3) was demonstrated by the photodecarboxylation of ketoprofen (KP, 2-(3-benzoylphenyl)propionic acid) under alkaline conditions (pH 10). In this method, a homogeneous solution comprising KP, calcium chloride, ammonia, and partially hydrolyzed poly(vinyl alcohol) (PVAPS, degree of saponification: 86.5-89.0 mol %) was used as the precursor solution and was exposed to ultraviolet (UV) irradiation for different time periods. Thermogravimetric analysis of the obtained xerogels showed that increasing the UV irradiation time increased the amount of CaCO3 formed and the complete conversion of calcium ions to calcite was achieved after 50 min of UV irradiation. Furthermore, solid phase analyses suggested that nanometer-to-micron-sized calcite crystals were formed and dispersed in the obtained PVAPS matrix.

  19. Synthesis of carbon nanotubes using the cobalt nanocatalyst by thermal chemical vapor deposition technique

    Energy Technology Data Exchange (ETDEWEB)

    Madani, S.S. [Department of Chemistry, Science and Research Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of); Zare, K. [Department of Chemistry, Science and Research Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of); Department of Chemistry, Shahid Beheshti University, Tehran (Iran, Islamic Republic of); Ghoranneviss, M. [Plasma Physics Research Center, Science and Research Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of); Salar Elahi, A., E-mail: Salari_phy@yahoo.com [Plasma Physics Research Center, Science and Research Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of)

    2015-11-05

    The three main synthesis methods of Carbon nanotubes (CNTs) are the arc discharge, the laser ablation and the chemical vapour deposition (CVD) with a special regard to the latter one. CNTs were produced on a silicon wafer by Thermal Chemical Vapor Deposition (TCVD) using acetylene as a carbon source, cobalt as a catalyst and ammonia as a reactive gas. The DC-sputtering system was used to prepare cobalt thin films on Si substrates. A series of experiments was carried out to investigate the effects of reaction temperature and deposition time on the synthesis of the nanotubes. The deposition time was selected as 15 and 25 min for all growth temperatures. Energy Dispersive X-ray (EDX) measurements were used to investigate the elemental composition of the Co nanocatalyst deposited on Si substrates. Atomic Force Microscopy (AFM) was used to characterize the surface topography of the Co nanocatalyst deposited on Si substrates. The as-grown CNTs were characterized under Field Emission Scanning Electron Microscopy (FESEM) to study the morphological properties of CNTs. Also, the grown CNTs have been investigated by High Resolution Transmission Electron Microscopy (HRTEM) and Raman spectroscopy. The results demonstrated that increasing the temperature leads to increasing the diameter of CNTs. The ideal reaction temperature was 850 °C and the deposition time was 15 min. - Graphical abstract: FESEM images of CNTs grown on the cobalt catalyst at growth temperatures of (a) 850 °C, (b) 900 °C, (c) 950 °C and (d) 1000 °C during the deposition time of 15 min. - Highlights: • Carbon nanotubes (CNTs) were produced on a silicon wafer by TCVD technique. • EDX and AFM were used to investigate the elemental composition and surface topography. • FESEM was used to study the morphological properties of CNTs. • The grown CNTs have been investigated by HRTEM and Raman spectroscopy.

  20. Dominant formation of the microsized carbon coils by a short time SF6 flow incorporation during the initial deposition stage.

    Science.gov (United States)

    Jeon, Young-Chul; Yi, Soung Soo; Kim, Sung-Hoon

    2013-08-01

    By SF6 gas incorporation for relatively short time during the initial deposition stage, carbon coils could be formed on nickel catalyst layer-deposited silicon oxide substrate using C2H2 and H2 as source gases under thermal chemical vapor deposition system. The characteristics (formation density and morphology) of as-grown carbon coils were investigated as a function of SF6 flow injection time. 5-min SF6 flow injection time is appropriate to produce the dominant microsized geometry for carbon coils without the appearance of the nanosized carbon coils. The geometry for the microsized carbon coils follows a typical double-helix structure and the shape of the rings constituting the coils is a flat-type. Fluorine's intrinsic etching characteristics for the nanosized carbon coils during the initial deposition stage seems to be the cause for the dominant formation of the microsized carbon coils in the case of 5-min SF6 flow injection time.

  1. Tilting of carbon encapsulated metallic nanocolumns in carbon-nickel nanocomposite films by ion beam assisted deposition

    Energy Technology Data Exchange (ETDEWEB)

    Krause, Matthias [Helmholtz-Zentrum Dresden-Rossendorf, PF-510119, 01314 Dresden (Germany); Technische Universitaet Dresden, D-01062 Dresden (Germany); Muecklich, Arndt; Zschornak, Matthias; Wintz, Sebastian; Gemming, Sibylle; Abrasonis, Gintautas [Helmholtz-Zentrum Dresden-Rossendorf, PF-510119, 01314 Dresden (Germany); Oates, Thomas W. H. [Leibniz-Institut fuer Analytische Wissenschaft, ISAS e.V., Albert-Einstein-Str. 9, 12489 Berlin (Germany); Luis Endrino, Jose [Surfaces and Coatings Department, Instituto de Ciencia de Materiales de Madrid, c/Sor Juana Ines de la Cruz 3, Cantoblanco, 28049 Madrid (Spain); Baehtz, Carsten; Shalimov, Artem [Helmholtz-Zentrum Dresden-Rossendorf, PF-510119, 01314 Dresden (Germany); Rossendorf Beamline, European Synchrotron Radiation Facility, F-38043 Grenoble (France)

    2012-07-30

    The influence of assisting low-energy ({approx}50-100 eV) ion irradiation effects on the morphology of C:Ni ({approx}15 at. %) nanocomposite films during ion beam assisted deposition (IBAD) is investigated. It is shown that IBAD promotes the columnar growth of carbon encapsulated metallic nanoparticles. The momentum transfer from assisting ions results in tilting of the columns in relation to the growing film surface. Complex secondary structures are obtained, in which a significant part of the columns grows under local epitaxy via the junction of sequentially deposited thin film fractions. The influence of such anisotropic film morphology on the optical properties is highlighted.

  2. Monodispersed calcium carbonate nanoparticles modulate local pH and inhibit tumor growth in vivo

    Science.gov (United States)

    Som, Avik; Raliya, Ramesh; Tian, Limei; Akers, Walter; Ippolito, Joseph E.; Singamaneni, Srikanth; Biswas, Pratim; Achilefu, Samuel

    2016-06-01

    The acidic extracellular environment of tumors potentiates their aggressiveness and metastasis, but few methods exist to selectively modulate the extracellular pH (pHe) environment of tumors. Transient flushing of biological systems with alkaline fluids or proton pump inhibitors is impractical and nonselective. Here we report a nanoparticles-based strategy to intentionally modulate the pHe in tumors. Biochemical simulations indicate that the dissolution of calcium carbonate nanoparticles (nano-CaCO3) in vivo increases pH asymptotically to 7.4. We developed two independent facile methods to synthesize monodisperse non-doped vaterite nano-CaCO3 with distinct size range between 20 and 300 nm. Using murine models of cancer, we demonstrate that the selective accumulation of nano-CaCO3 in tumors increases tumor pH over time. The associated induction of tumor growth stasis is putatively interpreted as a pHe increase. This study establishes an approach to prepare nano-CaCO3 over a wide particle size range, a formulation that stabilizes the nanomaterials in aqueous solutions, and a pH-sensitive nano-platform capable of modulating the acidic environment of cancer for potential therapeutic benefits.The acidic extracellular environment of tumors potentiates their aggressiveness and metastasis, but few methods exist to selectively modulate the extracellular pH (pHe) environment of tumors. Transient flushing of biological systems with alkaline fluids or proton pump inhibitors is impractical and nonselective. Here we report a nanoparticles-based strategy to intentionally modulate the pHe in tumors. Biochemical simulations indicate that the dissolution of calcium carbonate nanoparticles (nano-CaCO3) in vivo increases pH asymptotically to 7.4. We developed two independent facile methods to synthesize monodisperse non-doped vaterite nano-CaCO3 with distinct size range between 20 and 300 nm. Using murine models of cancer, we demonstrate that the selective accumulation of nano-CaCO3

  3. Synthesis of carbon nanotube array using corona discharge plasma-enhanced chemical vapor deposition

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    A corona discharge plasma-enhanced chemical vapor deposition with the features of atmospheric pressure and low temperature has been developed to synthesize the carbon nanotube array. The array was synthesized from methane and hydrogen mixture in anodic aluminum oxide template channels in that cobalt was electrodeposited at the bottom. The characterization results by the scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy and Raman spectroscopy indicate that the array consists of carbon nanotubes with the diameter of about 40 nm and the length of more than 4 -m, and the carbon nanotubes are mainly restrained within the channels of templates.

  4. Growth of straight carbon nanotubes by simple thermal chemical vapor deposition

    Institute of Scientific and Technical Information of China (English)

    ZOU Xiao-ping; H. ABE; T. SHIMIZU; A. ANDO; H. TOKUMOTO; ZHU Shen-ming; ZHOU Hao-shen

    2006-01-01

    Straight carbon nanotubes (CNTs) were achieved by simple thermal chemical vapor deposition(STCVD) catalyzed by Mo-Fe alloy catalyst on silica supporting substrate at 700 ℃. High-resolution transmission electron microscopy images show that the straight CNTs are well graphitized with no attached amorphous carbon. Mo-Fe alloy catalyst particles play a very crucial role in the growth of straight CNTs. The straight carbon nanotubes contain much less defects than the curved nanotubes and might have potential applications for nanoelectrical devices in the future. The simple synthesis of straight CNTs may have benefit for large-scale productions.

  5. Nanoscale Soldering of Positioned Carbon Nanotubes using Highly Conductive Electron Beam Induced Gold Deposition

    DEFF Research Database (Denmark)

    Madsen, Dorte Nørgaard; Mølhave, Kristian; Mateiu, Ramona Valentina

    2003-01-01

    We have developed an in-situ method for controlled positioning of carbon nanotubes followed by highly conductive contacting of the nanotubes, using electron beam assisted deposition of gold. The positioning and soldering process takes place inside an Environmental Scanning Electron Microscope (E...

  6. Microstructure and tribological performance of diamond-like carbon films deposited on hydrogenated rubber

    NARCIS (Netherlands)

    Pal, J.P. van der; Martinez Martinez, Diego; Pei, Y.T.; Rudolf, P.; Hosson, J.Th.M. De

    2012-01-01

    In this paper, the microstructure and tribological performance of diamond-like carbon (DLC) films prepared by plasma chemical vapor deposition on hydrogenated nitrile butadiene rubbers (HNBR) are studied. Different negative variations of temperature during film growth were selected by proper changes

  7. Industrial Scale Synthesis of Carbon Nanotubes Via Fluidized Bed Chemical Vapor Deposition: A Senior Design Project

    Science.gov (United States)

    Smith, York R.; Fuchs, Alan; Meyyappan, M.

    2010-01-01

    Senior year chemical engineering students designed a process to produce 10 000 tonnes per annum of single wall carbon nanotubes (SWNT) and also conducted bench-top experiments to synthesize SWNTs via fluidized bed chemical vapor deposition techniques. This was an excellent pedagogical experience because it related to the type of real world design…

  8. Energetic deposition of carbon in a cathodic vacuum arc with a biased mesh

    Science.gov (United States)

    Moafi, A.; Lau, D. W. M.; Sadek, A. Z.; Partridge, J. G.; McKenzie, D. R.; McCulloch, D. G.

    2011-04-01

    Carbon films were deposited in a filtered cathodic vacuum arc with a bias potential applied to a conducting mesh mounted in the plasma stream between the source and the substrate. We determined the stress and microstructural properties of the resulting carbon films and compared the results with those obtained using direct substrate bias with no mesh. Since the relationship between deposition energy and the stress, sp2 fraction and density of carbon are well known, measuring these film properties enabled us to investigate the effect of the mesh on the energy and composition of the depositing flux. When a mesh was used, the film stress showed a monotonic decrease for negative mesh bias voltages greater than 400V, even though the floating potential of the substrate did not vary. We explain this result by the neutralization of some ions when they are near to or passing through the negatively biased mesh. The microstructure of the films showed a change from amorphous to glassy carbonlike with increasing bias. Potential applications for this method include the deposition of carbon films with controlled stress on low conductivity substrates to form rectifying or ohmic contacts.

  9. Electroless Ni-B deposition from an emulsified supercritical carbon dioxide bath

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Hung-Yu; Chung, Sung-Ting; Chuang, Yan-Chi [Department of Materials Science and Engineering, National Chung Kung University, Tainan 70101, Taiwan (China); Tsai, Wen-Ta, E-mail: wttsai@mail.ncku.edu.t [Department of Materials Science and Engineering, National Chung Kung University, Tainan 70101, Taiwan (China)

    2010-10-01

    The electroless deposition of boron-containing Ni (EN-B) film from a supercritical carbon dioxide (sc-CO{sub 2}) bath was introduced. The deposition rate in sc-CO{sub 2} bath was one order of magnitude lower than that at ambient pressure without the presence of sc-CO{sub 2}. A more uniform chemical composition of the EN-B film could be obtained if it was deposited in the sc-CO{sub 2} bath. X-ray diffraction analyses revealed that the as-deposited film was amorphous in nature, despite of the deposition condition. Deposition defects such as cracks and voids could be avoided if the deposition was conducted in the sc-CO{sub 2} bath. Crystallization and boride precipitation were found after heat treatment at 400 {sup o}C for 1 h. The EN-B film deposited from the sc-CO{sub 2} bath had a higher hardness as compared with that of the normal EN-B coating. A substantial increase in hardness was obtained due to boride precipitation.

  10. Chemical and physical controls on the transformation of amorphous calcium carbonate into crystalline CaCO3 polymorphs

    Science.gov (United States)

    Blue, C. R.; Giuffre, A.; Mergelsberg, S.; Han, N.; De Yoreo, J. J.; Dove, P. M.

    2017-01-01

    Calcite and other crystalline polymorphs of CaCO3 can form by pathways involving amorphous calcium carbonate (ACC). Apparent inconsistencies in the literature indicate the relationships between ACC composition, local conditions, and the subsequent crystalline polymorphs are not yet established. This experimental study quantifies the control of solution composition on the transformation of ACC into crystalline polymorphs in the presence of magnesium. Using a mixed flow reactor to control solution chemistry, ACC was synthesized with variable Mg contents by tuning input pH, Mg/Ca, and total carbonate concentration. ACC products were allowed to transform within the output suspension under stirred or quiescent conditions while characterizing the evolving solutions and solids. As the ACC transforms into a crystalline phase, the solutions record a polymorph-specific evolution of pH and Mg/Ca. The data provide a quantitative framework for predicting the initial polymorph that forms from ACC based upon the solution aMg2+/aCa2+ and aCO32-/aCa2+ and stirring versus quiescent conditions. This model reconciles discrepancies among previous studies that report on the nature of the polymorphs produced from ACC and supports the previous claim that monohydrocalcite may be an important, but overlooked, transient phase on the way to forming some aragonite and calcite deposits. By this construct, organic additives and extreme pH are not required to tune the composition and nature of the polymorph that forms. Our measurements show that the Mg content of ACC is recorded in the resulting calcite with a ≈1:1 dependence. By correlating composition of these calcite products with the Mgtot/Catot of the initial solutions, we find a ≈3:1 dependence that is approximately linear and general to whether calcite is formed via an ACC pathway or by the classical step-propagation process. Comparisons to calcite grown in synthetic seawater show a ≈1:1 dependence. The relationships suggest that the

  11. Calcium carbonate saturation in the surface water of the Arctic Ocean: undersaturation in freshwater influenced shelves

    Directory of Open Access Journals (Sweden)

    A. Fransson

    2009-11-01

    Full Text Available In the summer of 2005, we sampled surface water and measured pH and total alkalinity (AT underway aboard IB Oden along the Northwest Passage from Cape Farewell (South Greenland to the Chukchi Sea. We investigated the variability of carbonate system parameters, focusing particularly on carbonate concentration [CO32−] and calcium carbonate saturation states, as related to freshwater addition, biological processes and physical upwelling. Measurements on AT, pH at 15°C, salinity (S and sea surface temperature (SST, were used to calculate total dissolved inorganic carbon (CT, [CO32−] and the saturation of aragonite (ΩAr and calcite (ΩCa in the surface water. The same parameters were measured in the water column of the Bering Strait. Some surface waters in the Canadian Arctic Archipelago (CAA and on the Mackenzie shelf (MS were found to be undersaturated with respect to aragonite (ΩAr<1. In these areas, surface water was low in AT and CT (<1500 μmol kg−1 relative to seawater and showed low [CO32−]. The low saturation states were probably due to the likely the effect of dilution due to freshwater addition by sea ice melt (CAA and river runoff (MS. High AT and CT and low pH, corresponded with the lowest [CO32−], ΩAr and ΩCa, observed near Cape Bathurst and along the South Chukchi Peninsula. This was linked to the physical upwelling of subsurface water with elevated CO2. The highest surface ΩAr and ΩCa of 3.0 and 4.5, respectively, were found on the Chukchi Sea shelf and in the cold water north of Wrangel Island, which is heavily influenced by high CO2 drawdown and lower CT from intense biological production. In the western Bering Strait, the cold and saline Anadyr Current carries water that is enriched in AT and

  12. Calcium carbonate saturation in the surface water of the Arctic Ocean: undersaturation in freshwater influenced shelves

    Directory of Open Access Journals (Sweden)

    M. Chierici

    2009-05-01

    Full Text Available In the summer of 2005, we sampled surface water and measured pH and total alkalinity (AT underway aboard IB Oden along the Northwest Passage from Cape Farwell (South Greenland to the Chukchi Sea. We investigated variability of carbonate system parameters, focusing particularly on carbonate concentration [CO32−] and calcium carbonate saturation states, as related to freshwater addition, biological processes and physical upwelling. Measurements on AT, pH at 15°C, salinity (S and sea surface temperature (SST, were used to calculate total dissolved inorganic carbon (DIC, [CO32−] and saturation of aragonite (ΩAr and calcite (ΩCa in the surface water. The same parameters were measured in the water column of the Bering Strait. Some surface waters in the Canadian Arctic Archipelago (CAA and on the Mackenzie shelf (MS were found to be undersaturated with respect to aragonite (ΩAr<1. In these areas, surface water was low in AT and DIC (<1500 μmol kg−1 relative to seawater and showed low [CO32−]. The low saturation states were probably due to the effect of dilution due from freshwater addition by sea ice melt (CAA and river runoff (MS. High AT and DIC and low pH, corresponded with the lowest [CO32−], ΩAr and ΩCa, observed near Cape Bathurst and along the South Chukchi Peninsula. This was linked to physical upwelling of subsurface water with elevated CO2. Highest surface ΩAr and ΩCa of 3.0 and 4.5, respectively, were found on the Chukchi Sea shelf and in the cold water north of Wrangel Island, which is heavily influenced by high CO2 drawdown and lower DIC from intense biological production. In the western Bering Strait, the cold and saline Anadyr Current carries water that is enriched in AT and DIC from enhanced organic matter remineralization, resulting in

  13. Gastric mucosal status susceptible to lanthanum deposition in patients treated with dialysis and lanthanum carbonate.

    Science.gov (United States)

    Ban, Shinichi; Suzuki, Syunji; Kubota, Kenji; Ohshima, Susumu; Satoh, Hideaki; Imada, Hiroki; Ueda, Yoshihiko

    2017-02-01

    Lanthanum carbonate is a popular chemical which is administered for patients with end-stage kidney disease to reduce the absorption of phosphate, and lanthanum deposition in the gastroduodenal mucosa has recently been reported. The aim of this study was to assess whether any histologic changes of the gastric mucosa are related to the deposition of lanthanum. Twenty-four patients who revealed the histology of lanthanum deposition on gastroduodenal biopsy between 2011 and 2014 were included in the study, and their clinical records and gastroduodenal biopsies obtained from 2011 to 2015 were reviewed, adding the review of gastroduodenal biopsies before 2011 if possible. Analysis of the deposited materials by scanning electron microscopy-energy dispersive x-ray spectroscopy was performed for a representative gastric biopsy. All patients were diagnosed as having renal insufficiency due to chronic kidney disease and treated with dialysis for more than 5 years, with confirmation of lanthanum carbonate use for 22 patients. Of 121 gastric biopsies and 10 duodenal ones between 2011 and 2015, 86 gastric biopsies (71.1%) and 3 duodenal biopsies (30%), respectively, revealed histology consistent with lanthanum deposition, which was confirmed by scanning electron microscopy-energy dispersive x-ray spectroscopy analysis for a representative case. The deposition tended to occur in the gastric mucosa with regenerative change, intestinal metaplasia, or foveolar hyperplasia (Pcarbonate is administered for patients with chronic kidney disease treated with dialysis.

  14. Interposition fixing structure of TiO2 film deposited on activated carbon fibers

    Institute of Scientific and Technical Information of China (English)

    FU Ping-feng; LUAN Yong; DAI Xue-gang

    2006-01-01

    The immobilized photocatalyst, TiO2 film supported on activated carbon fibers (TiO2/ACFs) prepared with molecular adsorption-deposition (MAD), exhibits high stability in cyclic photodegradation runs. The interposition fixing structure between TiO2 film and carbon fiber was investigated by means of SEM-EDX, XRD, XPS and FTIR, and a model was proposed to explain this structure. With SEM examination of carbon fiber surface after removing the deposited TiO2 film, a residual TiO2 super-thin film was found to exist still. By determining surface groups on ACFs, titanium sulfate (Ti2(SO4)3) in burnt remainders of the TiO2/ACFs was thought to be formed with an interfacial reaction between TiO2 film and carbon fibers. These provide some evidence of firm attachment of TiO2 film to carbon fiber surface. In the consideration of characteristics of the MAD, the deposition mechanism of TiO2 film on ACFs was proposed, and the interposition fixing structure was inferred to intercrossedly form between TiO2 film and ACFs' surface. This structure leaded to firm attachment and high stability of the TiO2 film.

  15. Synthesis and characterization of well-aligned carbon nitrogen nanotubes by microwave plasma chemical vapor deposition

    Institute of Scientific and Technical Information of China (English)

    马旭村; 徐贵昌; 王恩哥

    2000-01-01

    Well-aligned carbon nitrogen nanotube films have been synthesized successfully on meso-porous silica substrates by microwave plasma chemical vapor deposition (MWPCVD) method. Studies on their morphology, structure, and composition by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive X-ray spectroscopy (EDX), respectively, indicate that these nanotubes consist of linearly polymerized carbon nitrogen nanobells, and the nitrogen atoms have been doped into carbon netweork to form a new structure C1-xNx( x = 0.16±0.01). X-ray photoelectron spectroscopy (XPS) results of the samples further demonstrate that carbon bonds cova-lently with nitrogen in all the carbon nitrogen nanotube films.

  16. Self-organized formation of metal-carbon nanostructures by hyperthermal ion deposition

    Energy Technology Data Exchange (ETDEWEB)

    Hannstein, I.K.

    2006-04-26

    The quasi-simultaneous deposition of mass-selected hyperthermal carbon and metal ions results in a variety of interesting film morphologies, depending on the metal used and the deposition conditions. The observed features are of the order of a few nanometres and are therefore interesting for future potential applications in the various fields of nanotechnology. The present study focuses on the structural analysis of amorphous carbon films containing either copper, silver, gold, or iron using amongst others Rutherford Backscattering Spectroscopy, High Resolution Transmission Electron Microscopy, and Energy Dispersive X-Ray Spectroscopy. The film morphologies found are as follows: copper-containing films consist of copper nanoclusters with sizes ranging from about 3 to 9 nm uniformly distributed throughout the amorphous carbon matrix. The cluster size hereby rises with the copper content of the films. The silver containing films decompose into a pure amorphous carbon film with silver agglomerates at the surface. Both, the gold- and the iron-containing films show a multilayer structure of metal-rich layers with higher cluster density separated by metal-depleted amorphous carbon layers. The layer distances are of the order of up to 15 nm in the case of gold-carbon films and 7 nm in the case of iron-carbon films. The formation of theses different structures cannot be treated in the context of conventional self-organization mechanisms basing upon thermal diffusion and equilibrium thermodynamics. Instead, an ion-induced atomic transport, sputtering effects, and the stability of small metal clusters were taken into account in order to model the structure formation processes. A similar multilayer morphology was recently also reported in the literature for metal-carbon films grown by magnetron sputtering techniques. In order to investigate, whether the mechanisms are the same as in the case of the ion beam deposited films described above, first experiments were conducted

  17. Biologically formed calcium carbonate : a durable plugging agent for enhanced oil recovery

    Energy Technology Data Exchange (ETDEWEB)

    Nemati, M.; Voordouw, G. [Calgary Univ., AB (Canada)

    2002-06-01

    Waterflooding is a common enhanced oil recovery method in which water is injected into an oil reservoir. The flow is diverted into high permeability zones from which oil has already been recovered during primary production. The increased permeability variation decreases volumetric sweep efficiency of injected water. Cross flow complicates this problem by allowing flow between contrasting layers. This results in a ratio of produced water to oil that is much too high. The use of calcium carbonate (CaCO{sub 3}) and silica may be an effective method for selective plugging of reservoirs. The controlled biological formation of CaCO{sub 3} depends on the decomposition of urea to carbonate and ammonium ions by the catalytic action of urease enzyme. This study shows that biological formation of CaCO{sub 3} could be induced successfully using a bacterium with urease producing activity or urease enzyme. It is shown that the yield of enzymatically produced CaCO{sub 3} is substantially higher than when bacterially produced because the tolerable level of urea for bacteria is lower than the concentration of urea that participates in the enzymatic reaction. Plugging studies in unconsolidated porous media have shown that in situ formation of CaCO{sub 3} may decrease the permeability of porous media. The extent of plugging depends on the enzyme and reactant concentration. The extent of enzymatically produced CaCO{sub 3} increases with higher enzyme concentrations as well as with higher temperature. In situ formation of CaCO{sub 3} could result in a major decrease in permeability. 4 refs., 1 tab., 1 fig.

  18. Carbon deposition in CH4/CO2 operated SOFC: Simulation and experimentation studies

    Science.gov (United States)

    Girona, K.; Laurencin, J.; Fouletier, J.; Lefebvre-Joud, F.

    2012-07-01

    Due to their high operating temperatures, SOFCs can be directly fed with biogas, mainly composed of CH4 and CO2. In this work, experiments was performed with a classical Ni-YSZ cermet//YSZ//LSM cell fed either with a synthetic simulated biogas (CH4/CO2 ratio equal to 1 with 6% humidity), or with humidified H2. In both cases, the performances are found to be very similar, which confirms the ability of SOFCs to operate with internal reforming of biogas. Nevertheless, carbon formation in these operating conditions needs to be considered because of durability concerns. Thermodynamic calculations and modelling are carried out to evaluate the risk of carbon deposition depending on operating parameters. In the ternary diagram Csbnd Hsbnd O, the limits for carbon deposition are plotted, allowing the determination of “safe” operating conditions in terms of CH4 inlet flow rate and cell voltage. First experiments confirm these modelling results.

  19. Genesis of amorphous calcium carbonate containing alveolar plates in the ciliate Coleps hirtus (Ciliophora, Prostomatea).

    Science.gov (United States)

    Lemloh, Marie-Louise; Marin, Frédéric; Herbst, Frédéric; Plasseraud, Laurent; Schweikert, Michael; Baier, Johannes; Bill, Joachim; Brümmer, Franz

    2013-02-01

    In the protist world, the ciliate Coleps hirtus (phylum Ciliophora, class Prostomatea) synthesizes a peculiar biomineralized test made of alveolar plates, structures located within alveolar vesicles at the cell cortex. Alveolar plates are arranged by overlapping like an armor and they are thought to protect and/or stiffen the cell. Although their morphology is species-specific and of complex architecture, so far almost nothing is known about their genesis, their structure and their elemental and mineral composition. We investigated the genesis of new alveolar plates after cell division and examined cells and isolated alveolar plates by electron microscopy, energy-dispersive X-ray spectroscopy, FTIR and X-ray diffraction. Our investigations revealed an organic mesh-like structure that guides the formation of new alveolar plates like a template and the role of vesicles transporting inorganic material. We further demonstrated that the inorganic part of the alveolar plates is composed out of amorphous calcium carbonate. For stabilization of the amorphous phase, the alveolar vesicles, the organic fraction and the element phosphorus may play a role.

  20. Distinct Short-Range Order Is Inherent to Small Amorphous Calcium Carbonate Clusters (<2 nm)

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Shengtong [Physical Chemistry, University of Konstanz, Universitätsstrasse 10 78457 Konstanz Germany; School of Chemical Engineering, State Key Laboratory of Chemical Engineering, Shanghai Key Laboratory of Multiphase Materials Chemical Engineering, East China University of Science and Technology, 130 Meilong Road Shanghai 200237 P.R. China; Chevrier, Daniel M. [Department of Chemistry and Institute for Research in Materials, Dalhousie University, Halifax Nova Scotia B3H 4R2 Canada; Zhang, Peng [Department of Chemistry and Institute for Research in Materials, Dalhousie University, Halifax Nova Scotia B3H 4R2 Canada; Gebauer, Denis [Physical Chemistry, University of Konstanz, Universitätsstrasse 10 78457 Konstanz Germany; Cölfen, Helmut [Physical Chemistry, University of Konstanz, Universitätsstrasse 10 78457 Konstanz Germany

    2016-09-09

    Amorphous intermediate phases are vital precursors in the crystallization of many biogenic minerals. While inherent short-range orders have been found in amorphous calcium carbonates (ACCs) relating to different crystalline forms, it has never been clarified experimentally whether such orders already exist in very small clusters less than 2 nm in size. Here, we studied the stability and structure of 10,12-pentacosadiynoic acid (PCDA) protected ACC clusters with a core size of ca. 1.4 nm consisting of only seven CaCO3 units. Ligand concentration and structure are shown to be key factors in stabilizing the ACC clusters. More importantly, even in such small CaCO3 entities, a proto-calcite short-range order can be identified but with a relatively high degree of disorder that arises from the very small size of the CaCO3 core. Our findings support the notion of a structural link between prenucleation clusters, amorphous intermediates, and final crystalline polymorphs, which appears central to the understanding of polymorph selection.

  1. The kinetics and mechanisms of amorphous calcium carbonate (ACC) crystallization to calcite, via vaterite.

    Science.gov (United States)

    Rodriguez-Blanco, Juan Diego; Shaw, Samuel; Benning, Liane G

    2011-01-01

    The kinetics and mechanisms of nanoparticulate amorphous calcium carbonate (ACC) crystallization to calcite, via vaterite, were studied at a range of environmentally relevant temperatures (7.5-25 °C) using synchrotron-based in situ time-resolved Energy Dispersive X-ray Diffraction (ED-XRD) in conjunction with high-resolution electron microscopy, ex situ X-ray diffraction and infrared spectroscopy. The crystallization process occurs in two stages; firstly, the particles of ACC rapidly dehydrate and crystallize to form individual particles of vaterite; secondly, the vaterite transforms to calcite via a dissolution and reprecipitation mechanism with the reaction rate controlled by the surface area of calcite. The second stage of the reaction is approximately 10 times slo