Search results for "Oxide"

showing 10 items of 6424 documents

Influence of the preparation method on the thiophene HDS activity of silica supported CoMo catalysts

2002

Abstract The effect of the preparation method of CoMo/SiO2 catalysts with and without sodium ions, on the hydrodesulfurization (HDS) of thiophene was investigated by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and N2 physisorption (BET). The samples were prepared by total sol–gel route, by classic wetness impregnation and by co-impregnation, in the presence of nitrilotriacetic acid (NTA), of commercial and sol–gel prepared silica. The influence of sodium ions added to the sol mixture and to the silica before the impregnation with Co and Mo salt solution, was also considered. The presence of sodium favoured the phase transition of amorphous silica to cristobalite with con…

chemistry.chemical_compoundTransition metalchemistryPhysisorptionProcess Chemistry and TechnologyInorganic chemistryThiopheneOxideHeterogeneous catalysisCristobaliteHydrodesulfurizationCatalysisCatalysisApplied Catalysis A: General
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Role of Nitric Oxide for Modulation of Cancer Therapy Resistance

2010

Reactive nitrogen species (RNS) act as central second messengers in a balanced cellular network. While the complexity of nitric oxide (NO) signaling is far from being understood, and many controversial data can be found in the literature, there is evidence for NO as a major player of modulation of resistance to anticancer drugs and radiotherapy. Hypoxia in cancer tissues causes therapy resistance, and the hypoxia-inducing factor-1 (HIF-1) plays a predominant role in hypoxia-induced resistance. NO and NO-donating compounds sensitize tumor cells by inhibiting HIF-1 mediated transcription in hypoxic cells. Among a plethora of other genes, HIF-1-induced the transcription of the multidrug resist…

chemistry.chemical_compoundTumor suppressor geneChemistryDNA repairAngiogenesisDNA damageCancer researchNF-κBTranscription factorReactive nitrogen speciesNitric oxide
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The redox chemistry of gold with high-valence doped calcium oxide.

2012

chemistry.chemical_compoundValence (chemistry)ta114ChemistryInorganic chemistryDopingGeneral ChemistryGeneral MedicineCalcium oxideRedoxta116CatalysisAngewandte Chemie (International ed. in English)
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The initial stages of the heterogeneous degradation of alkali cellulose by oxygen in relation to the morphology of native cotton cellulose

2007

Treatment of cotton cellulose with sodium hydroxide solutions of varying concentration over extended periods in the absence of oxygen markedly decreases the intrinsic viscosity of both the cellulose in cuoxam and its cellulose trinitrate derivative (CTN) in acetone. Light-scattering measurements show that the molecular weight does not change while the radius of gyration decreases and the second virial coefficient increases. The narrow molecular weight distribution of the native cotton is still maintained. Mild oxidation first causes the intrinsic viscosity to increase. At more prolonged oxidation times the viscosity decreases. These results are interpreted by an intramolecular cross-linking…

chemistry.chemical_compoundViscosityChemical engineeringchemistryVirial coefficientSodium hydroxideIntrinsic viscosityPolymer chemistryGeneral EngineeringRadius of gyrationMolar mass distributionCelluloseAlkali metalJournal of Polymer Science: Polymer Symposia
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Recycling and fluxes of carbon gases in a stratified boreal lake following experimental carbon addition

2014

Partly anoxic stratified humic lakes are important sources of methane (CH4) and carbon dioxide (CO2) to the atmosphere. We followed the fate of CH4 and CO2 in a small boreal stratified lake, Alinen Mustajärvi, during 2007–2009. In 2008 and 2009 the lake received additions of dissolved organic carbon (DOC) with stable carbon isotope ratio (δ13C) around 16‰ higher than that of local allochthonous DOC. Carbon transformations in the water column were studied by measurements of δ13C of CH4 and of the dissolved inorganic carbon (DIC). Furthermore, CH4 and CO2 production, consumption and emissions were estimated. Methane oxidation was estimated by a diffusion gradient method. The amount, lo…

chemistry.chemical_compoundWater columnchemistryEcologyEpilimnionEnvironmental chemistryCarbon dioxideDissolved organic carbonAnaerobic oxidation of methanechemistry.chemical_elementCarbonAnoxic watersMethane
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A Theoretical and Experimental Study of Electrochemical pH Control at Gold Interdigitated Microband Arrays

2021

In electroanalysis, solution pH is a critical parameter that often needs to be adjusted and controlled for the detection of particular analytes. This is most commonly performed by the addition of chemicals, such as strong acids or bases. Electrochemical in-situ pH control offers the possibility for the local adjustment of pH at the point of detection, without additional reagents. FEA simulations have been performed to guide experimental design for both electroanalysis and in-situ control of solution pH. No previous model exists that describes the generation of protons at an interdigitated electrode array in buffered solution with one comb acting as a protonator, and the other as the sensor.…

chemistry.chemical_compoundWork (thermodynamics)Materials sciencechemistrypH indicatorReagentMethyl redElectrodeOxideAnalytical chemistryCyclic voltammetryElectrochemistry
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Epoxide Hydrolase Isoenzymes and their Individual Contribution to the Control of Toxic Metabolites

1991

Epoxides are highly strained three membered cyclic ethers which are formed in vivo by the microsomal cytochrome P450 dependent monooxygenases as intermediates of several important biosynthetic pathways (leukotriene A4, squalene 2, 3-oxide) and as metabolites of numerous xenobiotic compounds containing olefinic or aromatic double bonds. Further transformation of these epoxides may occur by either, rearrangement to phenols, aliphatic aldehydes, or ketones; by cytochrome P450 dependent reduction to the parent compound; or by spontaneous or enzymatic conjugation to gluta-thione. Epoxides may also bind covalently to cellular nucleophiles, such as proteins and nucleic acids thus eliciting carcino…

chemistry.chemical_compoundbiologychemistryBiochemistryLeukotriene A4Microsomal epoxide hydrolaseNucleic acidbiology.proteinCytochrome P450MonooxygenaseEpoxide hydrolaseXenobioticCarcinogen
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ChemInform Abstract: Palladium-Catalyzed Alkoxy- and Aminocarbonylation of α-Halomethyl Oxime Ethers: Synthesis of 1,3-Alkoxyimino Esters and 1,3-Alk…

2015

The three component reactions of α-bromomethyl oxime ethers, carbon monoxide, and alcohols or aromatic amines give imino esters and amides, respectively.

chemistry.chemical_compoundchemistryAlkoxy groupOrganic chemistrychemistry.chemical_elementheterocyclic compoundsGeneral MedicineOximeCarbonylationCatalysisCarbon monoxidePalladiumChemInform
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Reaktivitäut und reaktionswege von methylsubstituierten bisindolylcarbenium-ionen

1987

Methyl substituted bisindolylcarbenium ions 1 react with some O- and C-nucleophiles regioselectively. The cations 1b, 1c yield with hydroxide ions the tetraindolyldimethyl ether 4 and with methoxide ions the bisin-dolylmethoxymethanes 5. Compounds 1a, 1b, 1c react with several methylindoles to isomeric bis- and trisin-dolylmethanes. An electrophilic reactivity order of cations 1 can be derived supporting on the experimental results.

chemistry.chemical_compoundchemistryBicyclic moleculeYield (chemistry)Organic ChemistryElectrophileHydroxideReactivity (chemistry)EtherMethoxideCarbocationPhotochemistryMedicinal chemistryJournal of Heterocyclic Chemistry
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Synthesis of Linear and Cyclic Carbonates

2010

chemistry.chemical_compoundchemistryCarbon dioxideOrganic chemistry
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