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

Continuous industrial development increases energy consumption and, consequently, the consumption of fossil fuels. Coal mineral has been used in Brazil as a solid fuel for thermoelectric generators for several years. However, coal exploitation affects the environment intensely, mainly because Brazilian coal contains excess ash and pyrite (iron disulfide). According to the local coal industry syndicate, the average annual coal run per mine is 6 million ton/year; 3.5 million ton/year are rejected and disposed of in landfills. Besides pyrite, Brazilian coal contains Mn, Fe, Cu, Pb, Zn, Ge, Se, and Co. Additionally, the water used for coal beneficiation causes pyrite oxidation, forming an acid mine drainage (AMD). This drainage solubilizes the metals, transporting them into the environment, making treatment a requirement. This work deals with the use of sedimented residue from treated coal mine drainage sludge to obtain inorganic pigments that could be used in the ceramic industry. The residue was dried, ground and calcined ( approximately 1250 degrees C). The calcined pigment was then micronized (D(50) approximately 2mum). Chemical (XRF), thermal (DTA/TG), particle size (laser), and mineralogical (XRD) analyses were carried out on the residue. After calcination and micronization, mineralogical analyses (XRD) were used to determine the pigment structure at 1250 degrees C. Finally, the pigments were mixed with transparent glaze and fired in a laboratory roller kiln (1130 degrees C, 5min). The results were promising, showing that brown colors can be obtained with pigments made by residues.
 ...
PMID:Inorganic pigments made from the recycling of coal mine drainage treatment sludge. 1770 72

L-histidinium tetrafluorosuccinate (L-HFS), an organic nonlinear optical material has been synthesized and characterized by the elemental analysis, FT-IR, FT-NMR and X-ray diffraction studies. Solubility of L-HFS was found to be higher in water than ethanol. Single crystals with dimensions 10 mm x 6 mm x 3 mm were grown in an aqueous solution by the slow evaporation technique at 30 degrees C. The thermal stability of L-HFS has been analyzed by thermogravimetric and differential thermal analyses (TGA and DTA). The UV-vis spectral study reveals that the material has a wide optical transparency in the entire visible region with the lower cutoff wavelength at 235 nm. The phase matching condition was obtained by Kurtz powder second harmonic generation (SHG) efficiency test. The laser damage threshold of the grown crystal was measured using a Q-Switched Nd:YAG laser (1064 nm).
 ...
PMID:Crystal growth of phase matchable new organic nonlinear optical material for UV laser generation. 1776 2

A series of metal complexes were synthesized from equimolar amounts of Schiff bases: 1,4-bis[3-(2-hydroxy-1-naphthaldimine)propyl]piperazine (bappnaf) and 1,8-bis[3-(2-hydroxy-1-naphthaldimine)-p-menthane (damnaf) with metal chlorides. All of synthesized compounds were characterized by elemental analyses, spectral (UV-vis, IR, (1)H-(13)C NMR, LC-MS) and thermal (TGA-DTA) methods, magnetic and conductance measurements. Schiff base complexes supposed in tetragonal geometry have the general formula [M(bappnaf or damnaf)]Cl.nH(2)O, where M=Cr(III), Co(III) and n=2, 3. But also Fe(III) complexes have octahedral geometry by the coordination of two water molecules and the formula is [Fe(bappnaf or damnaf)(H(2)O)(2)]Cl. The changes in the selected vibration bands in FT-IR indicate that Schiff bases behave as (ONNO) tetradentate ligands and coordinate to metal ions from two phenolic oxygen atoms and two azomethine nitrogen atoms. Conductance measurements suggest 1:1 electrolytic nature of the metal complexes. The synthesized compounds except bappnaf ligand have the antimicrobial activity against the bacteria: Escherichia coli (ATCC 11230), Yersinia enterocolitica (ATCC 1501), Bacillus magaterium (RSKK 5117), Bacillus subtilis (RSKK 244), Bacillus cereus (RSKK 863) and the fungi: Candida albicans (ATCC 10239). These results have been considerably interest in piperazine derivatives due to their significant applications in antimicrobial studies.
 ...
PMID:Cr(III), Fe(III) and Co(III) complexes of tetradentate (ONNO) Schiff base ligands: synthesis, characterization, properties and biological activity. 1790 95

Water washed manganese nodule leached residue (WMNLR) calcined at different temperatures was characterized by XRD, FTIR, TG-DTA, surface area, surface oxygen, and surface acid sites. Surface area, surface oxygen, surface hydroxyl group, and surface acid sites increase up to 400 degrees C and then decrease with further rise in calcination temperature up to 700 degrees C. The catalytic activity of the calcined samples was tested for single-step oxidation of benzene to phenol using hydrogen peroxide as the oxidant and acetic acid as the solvent at room temperature. The influence of various reaction parameters such as solvent, concentration of solvent, oxidant amount, time, temperature, and catalyst amount was studied to optimize the reaction conditions. WMNLR calcined at 400 degrees C showed the highest catalytic activity towards oxidation of benzene with 12.7% conversion and 98% selectivity.
 ...
PMID:Surface characterization and catalytic evaluation of manganese nodule leached residue toward oxidation of benzene to phenol. 1790 63

We have combined hydrogen-bonding complexation in solution and layer-by-layer assembly for the controlled loading of a water-insoluble small organic molecule, bis-triazine (DTA), an azobenzene derivative containing multiple hydrogen bond donors and acceptors, into layer-by-layer multilayer films of poly(acrylic acid) and diazo-resin. UV-visible spectroscopy indicates that DTA has been loaded into multilayer films, with the loading amount increasing linearly with the number of layers. The loading amount can be well tuned either by changing the concentration of DTA or the solvent composition at the complexation step. Fourier transform infrared spectroscopy has revealed that both the complexation and layer-by-layer assembly are driven by hydrogen bonding. After photo-cross-linking and immersion in dimethyl sulfoxide to release DTA, the film can serve as an absorbent for DTA. This study provides a new unconventional layer-by-layer assembly that combines hydrogen-bonding complexation in solution and hydrogen-bond-driven layer-by-layer assembly at the interface. This method provides a new route to load a variety of water-insoluble functional organic molecules into layer-by-layer films.
 ...
PMID:Combining hydrogen-bonding complexation in solution and hydrogen-bonding-directed layer-by-layer assembly for the controlled loading of a small organic molecule into multilayer films. 1791 99

The mechanism for the decomposition of hydrotalcite remains unsolved. Controlled rate thermal analysis enables this decomposition pathway to be explored. Hydrotalcites containing carbonate, vanadate and molybdate were prepared by coprecipitation. The resulting materials were characterised by XRD, simultaneous TG-DTG-DTA and controlled rate thermal analysis (CRTA) to determine the stability and thermal decomposition pathway of the synthesised hydrotalcites. For the carbonate intercalated hydrotalcite dehydration takes place in three steps two of which are quasi-isothermal and one non-isothermal. Dehydroxylation and decarbonation occur separately over the 235-330 and 330-370 degrees C temperature range. A second non-isothermal decarbonation step is observed in the 371-541 degrees C range. In comparison the mixed carbonate-vanadate and carbonate-molybdate hydrotalcites show two dehydration steps and the dehydroxylation and decarbonation occur simultaneously. The observation of three dehydration steps is used to support the model of water molecules in three structurally distinct environments in the hydrotalcite interlayer. CRTA technology provides a mechanism for the decomposition of hydrotalcites.
 ...
PMID:Mechanism for hydrotalcite decomposition: a controlled rate thermal analysis study. 1799 79

Al-catechin/beta-cyclodextrin and Al-quercetin/beta-cyclodextrin (beta-CD) inclusion compounds were synthesized and characterized by IR, UV-vis, 1H and 13C NMR and TG and DTA analyses. Because quercetin is sparingly soluble in water, the stability constants of the Al-quercetin/beta-CD and Al-catechin/beta-CD compounds were determined by phase solubility studies. The AL-type diagrams indicated the formation of 1:1 inclusion compounds and allowed calculation of the stability constants. The thermodynamic parameters were obtained from the dependence of the stability constants on temperature and results indicated that the formation of the inclusion compounds is an enthalpically driven process. The thermal decomposition of the solid Al-quercetin/beta-CD and Al-catechin/beta-CD inclusion compounds took place at different stages, compared with the respective precursors, proving that an inclusion complexation process really occurred.
 ...
PMID:Synthesis and spectral investigation of Al(III) catechin/beta-cyclodextrin and Al(III) quercetin/beta-cyclodextrin inclusion compounds. 1805 38

The stability of monocalcium aluminate decahydrate, with the nominal composition CaAl(2)O(4).10H(2)O (CAH(10)), has a decisive role for the strength development and durability of cementitious materials based on high alumina cements. This has prompted an investigation of the thermal transformation of crystalline monocalcium aluminate decahydrate in air to an amorphous phase by in-situ synchrotron X-ray powder diffraction in the temperature range from 25 to 500 degrees C, by DTA/TGA, and (2)H, (27)Al MAS NMR spectroscopy. The decomposition includes the loss of hydrogen-bonded water molecules in the temperature range up to 175 degrees C, coupled with a reduction of the unit cell volume from 1928 A(3) at 25 degrees C, to 1674 A(3) at 185 degrees C. Furthermore, X-ray diffraction shows that CaAl(2)O(4).10H(2)O starts to transform to an amorphous phase at approximately 65 degrees C. This phase is fully developed at approximately 175 degrees C and it converts to crystalline CaAl(2)O(4) when heated to 1300 degrees C. The thermal decomposition in the temperature range from approximately 65 to approximately 175 degrees C involves both formation of an amorphous phase including AlO(4) tetrahedra and structural changes in the remaining crystalline phase.
 ...
PMID:Thermal decomposition of monocalcium aluminate decahydrate (CaAl2O4.10H2O) investigated by in-situ synchrotron X-ray powder diffraction, thermal analysis and 27Al, 2H MAS NMR spectroscopy. 1818 61

Ampicilline and nitrofurantoin, in both anhydrous and hydrate forms, were characterized by powder X-ray diffractometry (PXRD), thermogravimetric and differential thermal analyses (TG/DTA) and diffuse reflectance FT-IR spectroscopy (DRIFTS). Of all the analytical tools applied, only DRIFTS was able to indicate the formation of hydrogen bonds between the molecules of the anhydrous drug substance and crystalline water uptaken from atmospheric moisture as evidenced by the significant absorption at 3500-3700cm(-1) corresponding to crystal water. These results suggested that DRIFTS could provide information on hydration without a standard sample and accurately evaluate the physical stability focusing on the qualification of slight hydration in the early stages of pharmaceutical development. In addition, DRIFTS was applied to the besylate salt of pharmaceutical compound A to identify any possible hydration. This salt had the stable form BSA-I, metastable form BSA-II and hydrate form BSA-III. DRIFTS was able to show the hydration of BSA-II even when stored in a capped bottle, eventually leading to the transformation into BSA-III, which was not detected by PXRD. These findings verify the usefulness of DRIFTS for the solid-state characterization of pharmaceutical substances, especially the monitoring of gradual hydration.
 ...
PMID:Evaluation of hydrate formation of a pharmaceutical solid by using diffuse reflectance infrared Fourier-transform spectroscopy. 1819 25

In this work, Fe-doped mixed crystal TiO2 powder as sonocatalyst was prepared by the sol-gel method and heat treatment, and a novel method combined with ultrasonic irradiation was propounded to degrade the organic polluted water. First, the Fe-doped mixed crystal TiO2 powder was characterized by TG-DTA, XRD, and TEM techniques. Ultrasound was used as the irradiation source and the azo fuchsine was chose as the model compound. Then a series of degradation experiments was carried out in the presence of Fe-doped mixed crystal TiO2 powder. Also, the degradation process and some influencing factors, such as irradiation time, doping Fe3+ ion content, added amount of catalyst, and initial concentration of azo fuchsine solution, on the degradation were investigated by UV-vis spectra, ion chromatography, and HPLC. Through the degradation of azo fuchsine, it was found that the combination of ultrasonic irradiation and Fe-doped mixed crystal TiO2 powder can completely degrade the azo fuchsine in aqueous solution. Because of the good degradation efficiency, this method may be an advisable choice for the treatments of non- or low-transparent wastewaters in the future.
 ...
PMID:Preparation of Fe-doped mixed crystal TiO2 catalyst and investigation of its sonocatalytic activity during degradation of azo fuchsine under ultrasonic irradiation. 1820 58


<< Previous 1 2 3 4 5 6 7 8 9 10