Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:4.1.2.42 (DTA)
 1,693 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Crystallization kinetics studies for six experimental glass formulations in the system Na2O-CaO-SiO2-P2O5 synthesized by wet chemistry were conducted by means of differential thermal analysis. These glasses had CaO/P2O5 and SiO2/ (CaO + Na2O) ratios ranging from 8.74-3.38 and 0.92-3.03, respectively. Samples of each glass (n = 30 were heated from 23 to 1250 degrees C under N2 atmosphere at heating rates ranging from 10 to 50 degrees C/min. Glass-ceramics were obtained after heat treating the initial glasses at temperatures determined from their DTA exotherms. The activation energy of crystallization for each glass composition was calculated from an expression-relating log-heating rate and the reciprocal of the exothermic peak temperature. The compositions of the six glasses were significantly different (p = 0.05). The activation energy of crystallization (Q) values ranged from 196 to 782 kJ/mole. A correlation was obtained between Q and CaO/P2O5 and between Q and the Young's modulus (P < 0.001). Two of the six glasses exhibited bulk crystallization. X-ray diffraction studies showed that four of the six glasses exhibited different proportions of crystalline phases following heat treatment. These phases were wollastonite (CaSiO3), Na2CaSi3O9, combeite [Na4Ca3SI6O16(OH)2], and some unidentifiable phases. Two of the six bioceramic materials had a mixture of unknown crystalline phases.
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PMID:Crystallization of experimental bioactive glass compositions. 886 80

Glass-ceramic powders with the oxide batch formulation 50wt%SiO2, 20wt%P2O5 and 30wt%CaO were prepared by the sol-gel process using tetraethoxysilane, calcium nitrate and phosphoric acid as raw materials. The obtained gels and powders were characterized by TG-DTA thermal analysis, FTIR analyses and XRD measurements. The results indicated that (1) heating to more than 600 degrees C brought about elimination of -OC2H5 side chains from gels, and formation of a SiO2-based glass network, (2) crystallization such as Ca3(PO4)2 notably occurred in the SiO2-based glass matrix when heated to more than 900 degrees C, (3) -OH groups existed on SiO2-based glass-ceramic surfaces in the temperature region less than 900 degrees C, and (4) the melting point of this composition was more than 1400 degrees C. This study suggests that sol-gel-derived SiO2-based glass-ceramic powder containing P and Ca might be useful as bioactive implant materials.
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PMID:Characterization of 50wt%SiO2-20wt%P2O5-30wt%CaO glass-ceramic powders prepared by the sol-gel process. 955 50

The aim of this work was to investigate machinable glass-ceramics used as oral restoration material in K2O-MgO-Al2O3-SiO2-F glass system. By using of DTA, XRD and SEM investigation, the crystalline structure and characteristics were tested. The chemical composition of WCMM machinable glass-ceramics was defined by the following general formula: (K,Na)Mg3-3x Al2x (AlSi3) O10F2(0.5 < or = x < 0.7). The experimental results show that WCMM is an excellent oral restoration materials in the fabrication of crowns, inlayers and veneers.
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PMID:[The preliminary study on WCMM machinable glass-ceramics]. 1147 98

High silicon content SAPO(4)-5 (up to 0.511 atoms per unit cell) has been synthesised, using sodium 3-bromopropanesulfonate, sodium 1-butanesulfonate, sodium naphthalene-1-sulfonate or sodium n-decyl sulfate as surfactants; the SiO2 in the reaction gels ranged up to 3.0 (molar ratio), silicon incorporation was confirmed by XRD, XRF, TG-DTA, FT-IR and SEM techniques.
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PMID:Synthesis of high silicon content SAPO(4)-5 using anionic surfactants in a hexanol/aqueous two phase media. 1212 Mar 53

The siliceous skeletons of six hexactinellids and demosponges were compared using a series of physical and chemical tests. The sponges were two hermit-crab sponges (Class Demospongiae, family Suberitidae), one from Scotland, Suberites domuncula, and the other, Pseudospongosorites suberitoides, from the Gulf of Mexico, and four hexactinellids, Hyalonema sp., Euplectella aspergillum, Rhabdocalyptus dawsoni, and Aphrocallistes vastus. The operating hypothesis was that differences in the amorphous hydrated silica skeletons in Demosponges and Hexactinellids might prove taxonomically useful. Physical properties studied included SEM, glass density, glass transition temperature (Tg), TG/DTA to determine water content, and FTIR spectra. Chemical determinations were made using energy dispersive X-ray fluorescence (EDXRF). Spicular skeletal material is deposited in concentric layers around the axial canal. With the exception of differences at several bands in the IR spectra, the siliceous skeletons in demosponges and hexactinellids are largely indistinguishable. Density was similar in all sponges (range 2.03-2.13 g/cc) and similar to the density of opal (SiO2 x 1.5H2O) (mean = 2.09 g/cc). IR spectra were similar, with prominent absorption bands at 460-470, 800, and 1,090-1,100 cm(-1) (due to different vibrational modes of Si-O-Si linkages) and at 1,650 and 3,450-3,560 cm(-1) (due to water). The skeletons of all six showed similar spectra to that of silica gel both before and after heating to 1,200 degrees C. Water comprised 10-14% of the skeleton by weight, slightly higher in the demosponges. Average spicule chemical composition was 85.2% SiO2, 12.3% water, and 2.5% other elements (mainly S, Al, K, Ca, and Na). The percent amounts of Si did not differ significantly between the demosponges and the hexactinellids.
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PMID:Physical and chemical analysis of the siliceous skeletons in six sponges of two groups (demospongiae and hexactinellida). 1453 7

A simple external gelation process, taking full advantage of the gelation features of titanium and silica, was developed to prepare TiO2-SiO2 mixed gel spheres suitable for strontium adsorption. The source solutions used for the process were prepared from different mixtures of 1M TiCl4 and 1M Na2SiO3 solutions and converted into droplets in a gelation column. The suitable spheres for strontium adsorption were obtained using a hexone (methyl isobutyl ketone) solution as the drop formation medium and ammonia as the gelling agent. The mixed oxide gels were identified and characterized by DTA/TGA, FTIR and XRD analysis. The parameters affecting the strontium adsorption, such as weight ratio of TiO2, pH, temperature, shaking time and selectivity towards competing ions were investigated. Sorption data have been interpreted in terms of Freundlich, Langmuir and Dubinin-Radushkevich equations. Thermodynamic parameters for the sorption system have been determined at four different temperatures. The value of DeltaH degrees =39.553 kJ/mol and DeltaG degrees =-16.687 kJ/mol at 296 K prove that the sorption of strontium on mixed oxide gel is an endothermic and a spontaneous process.
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PMID:Preparation of TiO2-SiO2 mixed gel spheres for strontium adsorption. 1581 74

Sludge incinerated ash has been fired at different temperatures. This material was fired at 1050 degrees C for 3 h and until a peak of 1010 degrees C. After thermal treatment the ash was screened at 200 mesh.The ash was characterized by X-ray fluorescence and trace elements like Cr, Pb, Zn, Cu, and some oxides like quartz(SiO2), Al2O3, P2O5, Fe2O3 were found. Scanning electron microscopy(SEM) has shown one change of particle between 2 microm at 90 microm and apparent porosity, thermal analysis has shown loss of mass and residual decomposition in the TG, DTG and DTA curves.
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PMID:An experimental study of sewage sludge incineration. 1706 31

Simultaneous uptake of Ni2+, NH4+, and PO4(3-) by amorphous CaO-Al2O3-SiO2 (C-A-S) compounds was investigated using batch and column methods. Fifteen different C-A-S samples with systematically varied chemical compositions were prepared by coprecipitation from ethanol-water solutions containing Ca(NO3)2.4H2O, Al(NO3)3.9H2O, and Si(OC2H5)4, using NH4OH as the precipitating agent. The resulting precipitates were dried and heated at various temperatures to produce the C-A-S samples, which were then characterized by XRD, FTIR, solid state MAS NMR, DTA-TG, and N2 adsorption. All the C-A-S samples prepared at 600-900 degrees C were amorphous, apart from the CaO-rich samples. Simultaneous uptake of Ni2+, NH4+, and PO4(3-) was determined by a batch method using a solution with an initial concentration of 2 mM. In these experiments, the uptake abilities of the C-A-S samples for Ni2+ and PO4(3-) were high, but were relatively low for NH4+. The uptake abilities for Ni2+ and PO4(3-) increased but that for NH4+ decreased as the silica content in the C-A-S decreased, suggesting that similar uptake mechanisms (ion substitution and/or precipitation) are operating for Ni2+ and PO4(3-), but the uptake mechanism for NH4+ is different (physical adsorption). The column experiments indicate that the order of uptake ability of C-A-S for the three ions is NH4+ << PO4(3-) < Ni2+. Although the silica content of the C-A-S does not have the expected influence on the uptake of these three ions, for NH4+ it plays an important role in the formation of the amorphous phase and also in the suppression of Ca2+ and/or Al3+ release from the C-A-S during the uptake experiments. The optimum uptake properties of the C-A-S can thus be controlled by adjusting the chemical compositions and heating conditions under which the samples are prepared.
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PMID:Simultaneous uptake of Ni2+, NH4+ and PO4(3-) by amorphous CaO-Al2O3-SiO2 compounds. 1706 11

A new glass electrolyte formed by constant amounts of titanium oxide (TiO2) and various amount of phosphotungstic acid (PWA) doped P2O5-SiO2 is prepared using the sol-gel process. The structural formation is confirmed by Fourier infrared spectroscopy (FTIR) and from thermogravimetric and differential thermal analysis (TG/DTA) measurements, the glasses display good thermal stability. Further characterisation is undertaken by N2 adsorption/desorption measurements, proton conductivity and hydrogen permeability analyses and a H2/O2 fuel cell test is also performed. The glass materials with large pores and specific surface area are suitable for use as the electrolyte in H2/O2 fuel cells. The effect of TiO2 processing with constant amount of PWA in phosphosilicate glasses, is investigated and discussed. The hydrogen permeability is 1.57x10(-11) mol cm(-1) s(-1) Pa(-1) at 110 degrees C for 0.8 mm thick glass; a power density of 46.3 mW cm(-2) at 125 mA cm(-2) and a current density of 175 mA cm(-2) is obtained (T=28 degrees C, relative humidity).
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PMID:Development of new glass composite membranes and their properties for low temperature H2/O2 fuel cells. 1787 56

Tb3+ and Na2 WO4 co-doped SiO2 materials were prepared by sol-gel method and the structure of materials were measured by DTA-TG, IR and XRD techniques. The results indicate that the materials were in amorphous phase andthe Si-O-Si bond was still observed in samples annealed at 800 degrees C. The influence of Na2 WO4 on luminescence properties of terbium glasses was investigated by three-dimension fluorescence spectra, excitation and emission spectra. It is approve that when sample excited by 230 nm showed the characteristic emission peaks of terbium corresponding to 5D4-(7) Fj (j = 4, 5, 6) and 5 D3 -(7)Fj (j = 4, 5, 6) transitions. Doping Na2 WO4 has less influence with the emission position of SiO2 materials with terbium, but has a great effect with the emission intensity. It is find that the blue transition of 5D4-7F6 was activated and the green transition of 5D4-7F5 was quenched and the materials radiate green blue fluorescence light under ultraviolet light. The mechanism of sample was analyzed by the energy levels of Tb3+ and Na2 WO4 co-doped glasses.
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PMID:[Preparation and luminescence properties of Tb3+ ion and Na2WO4 co-doped SiO2 materials]. 1847 99


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