Search results for " Oxidation"

showing 10 items of 675 documents

Carbon nitride as photocatalyst in organic selective transformations

2020

Abstract Graphitic carbon nitride (g-C3N4) is a metal-free conjugated polymer which has become a new research hotspot in photocatalysis. It can be used for solar energy exploitation like in solar energy organic synthesis, one of the most new and appealing green applications of heterogeneous photocatalysis. This chapter resumes the state-of-the-art and progresses in the application of heterogeneous visible light photocatalysis in organic selective transformations by using C3N4 as photocatalyst.

chemistry.chemical_classificationMaterials sciencebusiness.industryGraphitic carbon nitrideNanotechnologyPolymerConjugated systemSolar energychemistry.chemical_compoundchemistryC-C formation Carbon nitride Coupling reactions Organic synthesis Organic transformations Partial oxidationPhotocatalysisOrganic synthesisSettore CHIM/07 - Fondamenti Chimici Delle TecnologiebusinessCarbon nitrideVisible spectrum
researchProduct

Reciprocal Enzymatic Interference of Carnitine Palmitoyltransferase I and Glycerol-3-Phosphate Acyltransferase in Purified Liver Mitochondria

2006

(i) Highly purified mitochondrial fractions were practically devoid of microsomal contamination and of acyl-CoA ligase activity. (ii) In mitochondria, glycerol-3-phosphate acyltransferase (GPAT) activity was supported by two enzymes, the first being very active at low palmitoyl-CoA / albumin ratios and sensitive to external agents (external form), the second being detected only at higher palmitoyl-CoA / albumin ratios and insensitive to external agents (internal form). (iii) Carnitine palmitoyltransferase I (CPT I) activity was shown to inhibit external GPAT activity only. (iv) Glycerol-3-phosphate exerted an inhibitory effect on CPT I, even when GPAT was inactive. Reciprocal interaction of…

chemistry.chemical_classificationMetabolic pathwayEnzymeBiochemistryChemistryAcyltransferaseMicrosomeCarnitine palmitoyltransferase ILigase activityMitochondrionBeta oxidation
researchProduct

Chemical and physico‐chemical changes during the dry‐cured processing of deer loin

2019

The changes on chemical composition, physico‐chemical parameters, free fatty acids and free amino acids content of dry‐cured deer loin were investigated at day 0, 30 and 60 of dry‐cured process. On the whole, except for pH values (≈5.6) and composition (fat: 4.6–5.2%; protein: ≈73%; ash: ≈17.5%) that did not show differences between the processing days, the other physico‐chemical parameters were affected by curing process. Colour parameters and moisture (from 69 to 38.4%) decreased while the hardness increase from 12.35 to 342 N and lipid oxidation (from 0.2 to 0.52 mg MDA/kg) increased as dry‐cured stage progresses. In similar way, free fatty acid (2250 mg per 100 g of fat at 0 day and 594…

chemistry.chemical_classificationMoisture0402 animal and dairy scienceFatty acid04 agricultural and veterinary sciencesLoin040401 food science040201 dairy & animal scienceIndustrial and Manufacturing Engineering0404 agricultural biotechnologyLipid oxidationchemistryLipolysisComposition (visual arts)Food scienceChemical compositionDry curedFood ScienceInternational Journal of Food Science & Technology
researchProduct

Photoelectrocatalytic selective oxidation of 4-methoxybenzyl alcohol in water by TiO2 supported on titanium anodes

2013

The photoelectrocatalytic partial oxidation of 4-methoxybenzyl alcohol in aqueous solution irradiated by near-UV light was carried out in a three-electrode batch reactor. TiO2 films were either deposited by dip-coating of a TiO2 sol onto a Ti foil and subsequent calcination or generated on Ti plates by thermal oxidation in air at 400-700 degrees C. The effects of the anode preparation method and bias potential values on conversion and selectivity to the corresponding aldehyde were investigated. The photoelectrocatalytic results were compared with the photocatalytic and electrocatalytic ones. The results indicated that no reaction occurred during the electrocatalytic experiments, whereas the…

chemistry.chemical_classificationPhotoelectrocatalysis Titanium TiO2/Ti 4-Methoxybenzaldehyde Aromatic alcohols Green synthesisProcess Chemistry and TechnologyInorganic chemistryAlcoholAldehydeCatalysislaw.inventionchemistry.chemical_compoundchemistrylawBenzyl alcoholSaturated calomel electrodePhotocatalysisCalcinationReactivity (chemistry)Partial oxidationGeneral Environmental Science
researchProduct

Modification of Polymers in Supercritical Carbon Dioxide

2003

The interaction of scFluids and polymers are governed by the intermolecular forces between solvent-solvent, solvent-polymer segment, and polymer segment-segment pairs. Because of its symmetry, within reasonable pressure values, CO2 does not have a dipole moment, but it does have a quadrupole moment significant over a much shorter distance than dipolar interactions. The quadrupole moment and the Lewis acidity of CO2 imparts to the carbon dioxide the peculiarity to be a solvent for selected classes of polymers like perfluorinated polyacrylates, polysiloxanes and polyether-polycarbonate diblock copolymers [1–3].

chemistry.chemical_classificationPhysics::Biological PhysicsQuantitative Biology::BiomoleculesSupercritical water oxidationSupercritical carbon dioxideMaterials scienceIntermolecular forcePolymerCondensed Matter::Soft Condensed MatterSolventDipolechemistryChemical physicsMoment (physics)QuadrupolePhysics::Chemical Physics
researchProduct

ChemInform Abstract: Oppenauer Oxidation of Secondary Alcohols with 1,1,1-Trifluoroacetone as Hydride Acceptor.

2008

1,1,1-Trifluoroacetone (2a) reacts as a hydride-acceptor in the Oppenauer oxidation of secondary alcohols (1) in the presence of diethylethoxyaluminum. The oxidant allows for selective oxidation of secondary alcohols in the presence of primary alcohols.

chemistry.chemical_classificationPrimary (chemistry)HydrideChemistryOppenauer oxidationGeneral MedicineBridged compoundsMedicinal chemistryAcceptorChemInform
researchProduct

Zur C-17-Oxidation von Clavinalkaloiden mit primärer alkoholischer Hydroxylgruppe

1975

Die Oppenauer-Oxidation von 1 mit Cyclohexanon fuhrt zu dem Aldolkondensationsprodukt 4 und der Carbonsaure 3. Analog konnte Lysergsaure (8) in geringer Menge aus 6 gewonnen und im Reaktionsgemisch von 7 nachgewiesen werden. Damit wurden erstmals Clavinalkaloide mit primarer alkoholischer Hydroxylgruppe chemisch zu den entsprechenden Carbonsauren oxidiert. C-17-Oxidation of Clavine Alkaloids with a Primary Alcoholic Hydroxyl Group. 1 is converted by Oppenauer oxidation with cyclohexanone to the aldol condensation product 4 and to the carboxylic acid 3. Lysergic acid (8) was obtained in a small yield by the analogous reaction of 6 and was found in the reaction mixture of 7. Thus clavine alka…

chemistry.chemical_classificationPrimary (chemistry)StereochemistryCarboxylic acidClavine AlkaloidsPharmaceutical ScienceCyclohexanoneOppenauer oxidationLysergic acidchemistry.chemical_compoundchemistryYield (chemistry)Drug DiscoveryAldol condensationArchiv der Pharmazie
researchProduct

Photocatalytic oxidation of aromatic alcohols to aldehydes in aqueous suspension of home-prepared titanium dioxide

2008

Abstract Oxygenated aqueous suspensions of home-prepared (HP) and commercial TiO2 catalysts were used in a batch photoreactor for carrying out the oxidation of benzyl alcohol (BA) and 4-methoxybenzyl alcohol (MBA) under different operative conditions. HP catalysts were synthesized from TiCl4 and underwent a hydrolysis treatment of different times under mild conditions. The textural characterization of catalysts was carried out with XRD, SEM observations, BET surface area and porosity measurements. For both alcohols the main oxidation products were the corresponding aromatic aldehydes and CO2. The HP catalysts exhibited selectivity values towards the aldehyde production up to 28% (BA convers…

chemistry.chemical_classificationProcess Chemistry and TechnologyButanolAlcoholAldehydeCatalysisCatalysischemistry.chemical_compoundchemistryBenzyl alcoholAlcohol oxidationOrganic chemistryMethanolPartial oxidationApplied Catalysis A: General
researchProduct

Influence of preparation conditions of nano-crystalline ceria catalysts on the total oxidation of naphthalene, a model polycyclic aromatic hydrocarbon

2007

Abstract Nano-crystalline ceria catalysts prepared by homogeneous precipitation with urea were tested for the total oxidation of naphthalene, a model polycyclic aromatic hydrocarbon (PAH). Systematic variation of preparation conditions, including calcination temperature, calcination time and aging time, resulted in differences in surface area, reducibility, morphology and crystallite size of the CeO 2 catalyst and hence differences in catalytic performance. A combination of high surface area, small crystallite size and high oxygen defect concentration was found to favor the efficiency of the ceria catalysts for the total oxidation of naphthalene. Optimum preparation conditions for this stud…

chemistry.chemical_classificationProcess Chemistry and TechnologyInorganic chemistryPolycyclic aromatic hydrocarbonHeterogeneous catalysisCatalysisCatalysislaw.inventionchemistry.chemical_compoundHydrocarbonCatalytic oxidationchemistrylawCalcinationCrystalliteGeneral Environmental ScienceNaphthaleneApplied Catalysis B: Environmental
researchProduct

SiO2-supported vanadium magnesium mixed oxides as selective catalysts for the oxydehydrogenation of short chain alkanes

2001

Abstract Unsupported and SiO 2 -supported VMgO mixed oxides catalysts have been prepared, characterized and tested in the oxidation of propane, n -butane and propylene. Mg-vanadates are observed by XRD, IR and Raman spectroscopy in both pure and supported VMgO catalysts, although the effective Mg/V ratio, in the VMgO phases formed, depends on the silica content. Since SiO 2 reacts partially with MgO during the calcination step, forming Mg 2 SiO 4 , the effective Mg/V ratio depends on the silica content. In this sense, pyro -Mg 2 V 2 O 7 is mainly formed on supported catalysts with Mg/V atomic ratios lower than 4, while ortho -Mg 3 V 2 O 8 is observed on supported catalysts with Mg/V atomic …

chemistry.chemical_classificationProcess Chemistry and TechnologyInorganic chemistryVanadiumchemistry.chemical_elementButaneCatalysisCatalysisPropenechemistry.chemical_compoundHydrocarbonchemistryPropaneAtomic ratioPartial oxidationApplied Catalysis A: General
researchProduct