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In order to investigate the effect of sintering temperature on the characteristics of sludge ceramsite and find an optimal sintering temperature, dried sewage sludge, clay, and water glass were mixed at ratios of dried sewage sludge/clay=33% and water glass/clay=15%. Then these mixtures were heated to 850, 900, 950, 1000, 1100, and 1200 degrees C for production of sludge ceramsite. The sludge ceramsite were characterized by DTA-TGA, SEM-EDS, XRD, and XRF. The results indicate that the differences in thermal behaviours are caused by the compositional and structural variations; the ceramsite sintered at 1000 degrees C has more uniformly distributed finer pores (0.5 microm<pore size<10.0 microm), while the ceramsite sintered at other temperatures has less pores and rougher surfaces. The main crystalline phases of ceramsite are quartz and kyanite below 1000 degrees C; kyanite is the main crystalline phase at 1000 and 1100 degrees C, and most of the crystalline phases are mullite at 1200 degrees C. It is therefore concluded that sintering temperature has a significant effect on the characteristics of sludge ceramsite, and that 1000 degrees C is the optimal sintering temperature.
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PMID:Effect of sintering temperature on the characteristics of sludge ceramsite. 1756 41

A novel class of orange-red phosphors based on Eu(3+)-activated LaNbTiO(6) was successfully fabricated by a wet chemical method, called a modified combustion approach. XRD, TG-DTA, SEM, and EDS results show that the heat-treatment of the powders above 1000 degrees C is enough to obtain highly crystallized and phase-pure LaNbTiO(6) and Eu(3+)-doped samples, which is of prime importance in investigating the optical properties of the novel phosphors using LaNbTiO(6) as the host material. UV-vis diffuse reflectance spectroscopy reveals that the direct band gap of LaNbTiO(6) with large grains (above 200 nm) is calculated to be 3.27 eV, while the absorption edge of the small particles shows an obvious blue-shift. Two blue emission bands centered at 440 and 470 nm ascribed to the self-trapped exciton emission of the distorted NbO(6) and TiO(6) groups for the pure LaNbTiO(6) can be obtained. Photoluminescence spectra of the Eu(3+)-doped phosphor particles illuminated the simultaneous occurrence of several intense orange-red band emissions due to the characteristic transitions of (5)D(0,1) --> (7)F(J) (J = 0, 1, 2, 3, 4) of Eu(3+) under 395 nm excitation. The mechanism of these multiplets possibly arising from the odd-parity distortions of the Eu(3+) ion environment and the effect of crystallanity of the compounds on luminescence were discussed, respectively. The highly bright and color-uniform fluorescence images of the doped samples with short luminescence decay times (nanosecond magnitude) confirmed the potential applications of the phosphors in luminescence and display devices.
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PMID:Novel class of aeschynite structure LaNbTiO6-based orange-red phosphors via a modified combustion approach. 1793 5

Adsorption-based processes are widely used in the treatment of dilute metal-bearing wastewaters. The development of versatile, low-cost adsorbents is the subject of continuing interest. This paper examines the preparation, characterization and performance of a micro-scale composite adsorbent composed of silica gel (15.9 w/w%), calcium silicate hydrate gel (8.2 w/w%) and calcite (75.9 w/w%), produced by the accelerated carbonation of tricalcium silicate (C(3)S, Ca(3)SiO(5)). The Ca/Si ratio of calcium silicate hydrate gel (C-S-H) was determined at 0.12 (DTA/TG), 0.17 ((29)Si solid-state MAS/NMR) and 0.18 (SEM/EDS). The metals-retention capacity for selected Cu(II), Pb(II), Zn(II) and Cr(III) was determined by batch and column sorption experiments utilizing nitrate solutions. The effects of metal ion concentration, pH and contact time on binding ability was investigated by kinetic and equilibrium adsorption isotherm studies. The adsorption capacity for Pb(II), Cr(III), Zn(II) and Cu(II) was found to be 94.4 mg/g, 83.0 mg/g, 52.1 mg/g and 31.4 mg/g, respectively. It is concluded that the composite adsorbent has considerable potential for the treatment of industrial wastewater containing heavy metals.
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PMID:Characterization of carbonated tricalcium silicate and its sorption capacity for heavy metals: a micron-scale composite adsorbent of active silicate gel and calcite. 1795 Sep 99

Chitosan a natural based polymer is non-toxic, biocompatible and biodegradable. Chemical modification of chitosan to generate new bifunctional materials and finally would bring new properties depending on the nature of the group introduced. In our present study, we prepared phosphorylated chitosan (P-chitosan) by using H(3)PO(4)/P(2)O(5)/Et(3)PO(4)/hexanol method. From our present method, we got high yield and high degree of substitution (DS). The prepared P-chitosan (DS-1.18) was characterized by FT IR, (13)C NMR, (31)P NMR, elemental, XRD, TGA, DTA and SEM studies. After the phosphorylation, the solubility of the polymer was improved. The P-chitosan showed less thermal stability and crystallinity than the chitosan. It was due to the phosphorylation.
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PMID:Synthesis of phosphorylated chitosan by novel method and its characterization. 1827 50

The aim of this work was to gain a better understanding about the synthesis of tetracalcium phosphate (TTCP, Ca(4)(PO(4))(2)O) through a solid-state reaction from mechanochemically activated CaCO(3)-(NH(4))(2)HPO(4) mixtures. The evolution of the reaction was followed by DTA, XRD, FTIR and SEM techniques. An enhanced reactivity of the mixtures was detected as the mechanochemical treatment times increased. This effect was related to both the loss of crystallinity of the reactants and the production of defects on their surfaces. 6 h of mechanochemical processing at 1190 rpm, followed by 3 h of thermal treatment at 1500 degrees C, were enough to obtain pure TTCP. The crystallinity and purity of the obtained TTCP were checked by XRD and FTIR. The morphologic characteristics were analyzed by SEM and BET analysis. The behavior of synthesized TTCP powder in combination with commercial dicalcium phosphate anhydrous (DCPA, CaHPO(4)), as the solid phase of bone cements, was tested. Both the combination of different particle sizes of TTCP and DCPA and the effect of different kinds of accelerator agents (disodium hydrogen phosphate, tartaric acid, citric acid and oxalic acid) on setting time and degree of conversion to hydroxyapatite (HA, Ca(10)(PO(4))(6)(OH)(2)) were evaluated. The combination of TTCP (0.32 m(2)/g) with DCPA (1.52 m(2)/g), in a 1/1 molar ratio, showed the shortest setting times and high conversions to HA when an oxalic acid solution (5% volume fraction) was used as the liquid phase of the formulation. Results obtained from this work demonstrated that synthesized TTCP shows promising behavior as a component of bone cements, exhibiting not only a smaller particle size than that usually reported but also a low degree of crystallinity, all of which increases the reactivity of the obtained TTCP. This study provided a very efficient method for synthesizing pure TTCP through a modified solid-state reaction from mechanochemically activated reactants, employing very short times of thermal treatment in comparison with the conventional processes.
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PMID:Synthesis of tetracalcium phosphate from mechanochemically activated reactants and assessment as a component of bone cements. 1830 3

Metal complexes of o-vanillidene-2-aminobenzothiazole have been prepared and characterized by elemental and spectral (vibrational, electronic, 1H NMR and EPR) data as well as magnetic susceptibility measurements and thermo gravimetric analysis (TG/DTA). The low molar conductance values reveal the non-electrolytic nature of these complexes. The elemental analysis suggests that the stoichiometry to be 1:2 (metal:ligand). Magnetic susceptibility data coupled with electronic spectra suggest that two ligands coordinate to each metal atom by phenolic oxygen and imino nitrogen to form high spin octahedral complex with Co(II), Mn(II) and Ni(II). The fifth and sixth position of metal ion is satisfied with water molecules. The thermal behaviour (TG/DTA) of the synthesised complexes shows that the complexes loss water molecules in the first step followed by decomposition of the ligand. Spin Hamiltonian parameters predict a distorted tetrahedral geometry for the copper complex. XRD and SEM analysis provide the crystalline nature and the morphology of the metal complexes. The in vitro biological activity of the metal chelates is tested against the Gram positive bacteria (Bacillus amyloliquifacians) and gram negative bacteria (Pseudomonas species), fungus (Aspergillus niger) and yeast (Sacchromyces cereviaceae). Most of the metal chelates exhibited higher biological activities.
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PMID:Spectral, XRD, SEM and biological activities of transition metal complexes of polydentate ligands containing thiazole moiety. 1831 76

Iron oxide thin films were prepared by spin-coating a gel solution of iron(III) nitrate dissolved in 2-methoxyethanol and acetylacetone on glass and quartz substrates. The film thickness was adjusted by changing the spinning rate of the spin coater. Annealing was carried out between 300 degrees C to 600 degrees C to investigate the phases present in the films. Viscosity of the main solution was found as 0.0035 Pa.s by viscosity measurement. TGA/DTA analyses showed that heat treatment should be done between 330 degrees C and 440 degrees C in order to produce maghemite thin films. SEM studies showed that single layer thickness of the films were between 65 and 80 nm. The structural characteristics were evaluated by changing the experimental parameters which are annealing temperature, annealing time and thickness of the films. From the X-ray diffraction analysis, maghemite formation was observed with decreasing annealing temperature, annealing time and film thickness. TEM results verified the presence of the maghemite phase by electron diffraction and selected area electron diffraction (SAED) methods. According to UV-Vis results transmittance of the films decreases with increasing annealing temperature.
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PMID:Characterization of iron oxide thin films prepared by sol-gel processing. 1846 25

A self-assembled right handed helical ribbon of bone mineral, hydroxyapatite (HAp) was crystallized in sodium meta silicate gel matrix at 27 degrees C and the physiological pH (7.4). At temperatures 37 and 47 degrees C, helical structures were followed by many Liesegang rings. The samples were characterized by FT-IR, XRD, SEM, ICP-OES and TG-DTA techniques. The helical ribbon consisted of platy Ca-deficient apatite crystals of size 2.8 microm. Liesegang ring had a continuous network of fibers with interconnected pores. The samples exhibited bioactivity when soaked in SBF.
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PMID:Self-assembled right handed helical ribbons of the bone mineral hydroxyapatite. 1856 88

Adsorption of aflatoxin B(1) (AFB1) by natural montmorillonite (MONT) and montmorillonite modified with copper ions (Cu-MONT) was investigated. Both MONTs were characterized using the X-ray powder diffraction (XRPD) analysis, thermal analysis (DTA/TGA) and scanning electron miscroscopy/electron dispersive spectroscopy (SEM/EDS). The results of XRPD and SEM/EDS analyses of Cu-MONT suggested partial ion exchange of native inorganic cations in MONT with copper occurred. Investigation of AFB1 adsorption by MONT and Cu-MONT, at pH 3, 7 or 9, showed that adsorption of this toxin by both MONTs was high (over 93%). Since AFB1 is nonionizable, no differences in AFB1 adsorption by both MONTs, at different pHs, were observed, as expected. Futhermore, it was determined that adsorption of AFB1 by both MONTs followed a non-linear (Langmuir) type of isotherm, at pH 3. The calculated maximum adsorbed amounts of AFB1 by MONT (40.982mg/g) and Cu-MONT (66.225mg/g), derived from Langmuir plots of isotherms, indicate that Cu-MONT was much effective in adsorbing AFB1. Since, the main cation in an exchangeable position in MONT is calcium, and in Cu-MONT both calcium and copper, the fact that ion exchange of inorganic cations in MONT with copper increases adsorption of AFB1 suggests that additional interactions between AFB1 and copper ions in Cu-MONT caused greater adsorption.
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PMID:Aflatoxin B(1) adsorption by natural and copper modified montmorillonite. 1858 10

TiO2 pillared montmorillonite composite photocatalyst was synthesized by acid-catalyzed sol method and characterized by IR, UV-Vis, TG/DTA, XRD, SEM etc. Spectral analyses have demonstrated that TiO2 pillared montmorillonite(Ti-MMT) has wider interlayer distance than Na substituted montmorillonite (Na-MMT) and higher optical absorption efficiency than nanoscale anatase TiO2. The photocatalytic degradation reaction of acidic fuchsine by sunlight was employed to evaluate the catalytic activity of the composite catalyst. It was found that, besides easy reclaimation, the photocatalytic activity of the catalyst was much higher than that of the pure nanosized anatase TiO2. When the addition amount of Ti-MMT is 0.2 g x (100 mL)(-1) and pH of acidic fuchsine solution is 3, the dye could be degraded thoroughly in 40 min and the degradation reaction obeys Langmuir- Hinshelwood equation.
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PMID:[Preparation of TiO2 pillared montmorillonite photocatalyst and its photocatalytic activity to degradation reaction of acidic fuchsine by sunlight]. 1872 Aug 15


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