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)

After nano-particles (ZnO) had been encapsulated by a kind of water-soluble cellulose Hydoxyl-Propyl-Methyl Cellulose (HPMC), then methyl methacrylate was grafted onto the surface of them. Thus the surface of nano-ZnO had been successfully modified. FTIR, DTA and TEM were utilized to confirm the results. FTIR shows that HPMC was adsorbed onto the surface of ZnO, and PMMA was also grafted onto its surface, DTA says that the heat stability of HPMC, HPMC-g-PMMA and ZnO/HPMC-g-PMMA increased greatly, TEM photo demonstrates that polymer adhered onto the surface of nano-ZnO which was encapsulated by a layer of film-like polymer.
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PMID:[Chemical modification on the surface of nano-particles of ZnO and its characterization]. 1576 10

Polyvinylpyrrolidone (PVP)-modified CdS nanorods were prepared by a hydrothermal reaction of CdCl2 2.5H2O and (NH4)2S with 10 wt% ethylenediamine aqueous solution as solvent and 1.0 wt% PVP as additives. The obtained products were characterized by means of XRD, TEM, IR, DTA-TG, UV-Vis and PL spectroscopies. The surface-modified CdS nanorods showed narrow size distribution and enhanced luminescence property compared with that of the unmodified ones. The UV-Vis spectra exhibited a structure peak. These results were attributed to the surface passivation of the CdS nanorods by the PVP molecules.
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PMID:[Preparation and spectral properties of PVP-modified CdS nanorods]. 1620 86

Fine composite powders of yttria (3 mol%) stabilized zirconia (Z, 10 wt%) and hydroxyapatite (HA), denoted as HAZ, were prepared by the co-precipitation method. The resulting powders were characterized by XRF, TEM, EDS, XRD, FTIR, TG-DTA, and BET surface area techniques. AES and FTIR were employed to determine the surface properties of the HAZ suspensions in the presence of NH4PAA as a dispersant, which confirmed that the surfaces of both HA and Z were affected by the adsorbed polymers. The mechanism of NH4PAA adsorption on the particles was discussed. Zeta potential measurements showed that the addition of NH4PAA resulted in a dramatic increase in the absolute value of zeta potential. NH4PAA considerably enhanced the stability of the HAZ suspension via electrosteric barrier mechanisms. TEM micrographs confirmed that particles were well dispersed in the suspension. The adsorption density of the dispersant was found to decrease with an increase in pH value.
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PMID:Fabrication and surface characterization of NH4PAA-stabilized HAZ suspensions. 1625 23

A simple and effective method for synthesizing silica hollow spheres is presented. The synthesis utilizes vesicles from oppositely charged surfactants sodium dodecyl sulfate (SDS) and tetrapropylammonium bromide (TPAB) aqueous solution as template for the silica growth. Tetraethyl orthosilicate (TEOS) is added to the vesicular template as a precursor for the silica formation. Ultrasound was employed to accelerate the formation of vesicles template. The morphology of the silica spheres is uniform and well-defined (diameter: 200 nm-5 microm, wall thickness: 50 nm). The product was also characterized by FTIR, TG-DTA, N2 adsorption. TEM images reveal that the spheres have structure stability after calcinations at 550 degrees C.
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PMID:Synthesis of silica hollow spheres assisted by ultrasound. 1629 99

This paper describes the fabrication of barium strontium titanate (Ba0.6Sr0.4TiO3 or BST) nanofibers by electrospinning method using a solution that contained poly(vinylpyrrolidone) and a sol-gel solution of BST. The as-spun and calcined BST/PVP composite nanofibers were characterized by TG-DTA, X-ray diffraction, FT-IR, SEM and TEM, respectively. After calcination of the as-spun BST/PVP composite nanofibers at above 700 degrees C in air for 2 h, BST nanofibers of 188+/-25 nm in diameter having well-developed cubic-perovskite structure were successfully obtained. The crystal structure and morphology of the nanofibers were influenced by the calcination temperature. Calcination at below 700 degrees C resulted in amorphous phase whereas BST with second phase such as barium titanate were formed at above 700 degrees C. Diameters of the nanofibers decreased from 208+/-35 to 161+/-18 nm with increasing calcination temperature between 600 and 800 degrees C.
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PMID:Nanofibers of barium strontium titanate (BST) by sol-gel processing and electrospinning. 1633 72

Long persistent phosphoresceoce CaAl2O4:Eu2+, Nd3+ nanoparticles were synthesized through sol-gel method. The structures and properties of the samples were analyzed by DTA, TGA, XRD, TEM and spectrometer. Results indicated that the CaAl2O4 crystalline phase was formed at 800 degrees C. The particles are spherical in shape and about 20-40 nm in size. The peaks of the excitation, emission and thermoluminescence spectra shift compared with the CaAl2O4: Eu2+,Nd3+ coarse crystals. The luminescence decay includes a initial rapid part and a following slow part. The decay time lasts for about 5 h.
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PMID:[Preparation and characterization of CaAl2O4:Eu2+, Nd3+ nanoparticles]. 1639 82

The present study reports a green synthesis method for preparing pure (free of fly ash) and ordered MCM-41 materials from coal fly ash at room temperature (25 degrees C) during 24 h of reaction. It was shown that the impurities in the coal fly ash were not detrimental to the formation of MCM-41 at the tested conditions. The influence of initial synthesis pH on material properties of calcined MCM-41 samples was investigated by various techniques such as XRF, XPS, XRD, FTIR, DR-UV-vis, solid state NMR, N2 physisorption, TG-DTA, SEM and TEM. The experimental results showed that the amount of trace elements such as Al, Na, Ti and Fe incorporated into the sample increased with synthesis pH value. More aluminum species were incorporated with tetrahedral coordination in the framework under a high pH value. The particle size of the sample decreased with the synthesis pH value. Samples synthesized at high pH values had a larger pore size and were more hydrothermally stable than those at low pH values. From thermal analysis, it was observed that the synthesized MCM-41 samples showed a high thermal stability. These properties made the synthesized MCM-41 suitable for further processing into more useful materials in a wide range of applications.
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PMID:Synthesis of MCM-41 from coal fly ash by a green approach: influence of synthesis pH. 1664 13

Biphasic beta-rhenanite (beta-NaCaPO(4))-hydroxyapatite (Ca(10)(PO(4))(6)(OH)(2)) biomaterials were prepared by using a one-pot, solution-based synthesis procedure at the physiological pH of 7.4, followed by low-temperature (300-600 degrees C) calcination in air for 6 h. Calcination was for the sole purpose of crystallization. An aqueous solution of Ca(NO(3))(2). 4H(2)O was rapidly added to a solution of Na(2)HPO(4) and NaHCO(3), followed by immediate removal of gel-like, poorly-crystallized precursor precipitates from the mother liquors of pH 7.4. Freeze-dried precursors were found to be nanosize with an average particle size of 45 nm and a surface area of 128 m(2)/g. Upon calcination in air, precursor powders crystallized into biphasic (60% HA-40% rhenanite) biomaterials, while retaining their submicron particle sizes and high surface areas. beta-rhenanite is a high solubility sodium calcium phosphate phase. Samples were characterized by XRD, FTIR, SEM, TEM, ICP-AES, TG, DTA, DSC, and surface area measurements.
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PMID:A new rhenanite (beta-NaCaPO(4)) and hydroxyapatite biphasic biomaterial for skeletal repair. 1676 21

In this paper, surface physiochemical properties of three typical aluminas, gamma-Al(OH)3, gamma-Al2O3, and alpha-Al2O3, were investigated by means of XRD, SEM, TEM, BET surface area, TG/DTA, and potentiometric titration techniques. Based on the titration data, surface protonation and deprotonation constants were determined using the constant capacitance model (CCM). The emphasis of this research was laid on the comparison of the crystal structure, surface hydration/dehydration and acid-base properties of these three typical alumina minerals. The calculation results revealed that the surface acidity of the aluminas is in the order of alpha-Al2O3>gamma-Al(OH)3>gamma-Al2O3 after being hydrated for 1 h. The correlation between the hydration/dehydration mechanisms of alumina and its acid/base properties is discussed.
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PMID:Surface acid-base properties and hydration/dehydration mechanisms of aluminum (hydr)oxides. 1727 18

Anatase-type TiO2 single nanocrystals with boatlike, comblike, sheetlike, leaflike, quadrate, rhombic, and wirelike particle morphologies were prepared by hydrothermal treatment of a layered titanate nanosheet colloidal solution. The formation reactions and surface properties of the TiO2 nanocrystals were investigated using XRD, TEM, TG-DTA analyses, and measurements of BET specific surface area, photocatalytic activity, and ruthenium dye (N719) adsorption. The crystal morphology can be controlled by reaction temperature, pH value of reaction solution, and exfoliating agent. The titanate nanosheets were transformed to the TiO2 nanocrystals by two types of reactions. One is an in situ topotactic structural transformation reaction, and the other is a dissolution-deposition reaction on the surface. The anatase nanocrystals formed by the in situ topotactic structural transformation reaction retain the sheetlike particle morphology of the precursor, and they preferentially expose the (010) plane of anatase structure. The crystal surface of anatase nanocrystals prepared in this study showed higher photocatalytic activity and higher ruthenium dye adsorption capacity than did the Ishihara ST-01 sample, a standard anatase nanocrystal sample. The results indicated the (010) plane of the anatase structure has high photocatalytic activity and high ruthenium dye adsorption ability.
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PMID:Single nanocrystals of anatase-type TiO2 prepared from layered titanate nanosheets: formation mechanism and characterization of surface properties. 1793 63


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