Search results for "Alcohol"

showing 10 items of 1798 documents

Home-prepared anatase, rutile, and brookite TiO2 for selective photocatalytic oxidation of 4-methoxybenzyl alcohol in water: reactivity and ATR-FTIR …

2009

5th European Meeting on Solar Chemistry and Photocatalysis -- OCT 04-08, 2008 -- Palermo, ITALY

AnataseSettore ING-IND/24 - Principi Di Ingegneria ChimicaAldehydesCatalystsChemistryBrookiteInorganic chemistryAlcoholSelective photooxidation 4-methoxybenzylalcohol TiO2 ATR-FTIRP-anisaldehydeCatalysischemistry.chemical_compoundOrganic-chemistryGreen routeRutilevisual_artvisual_art.visual_art_mediumPhotocatalysisAqueous suspensionReactivity (chemistry)Partial oxidationSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysical and Theoretical Chemistry
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Photocatalytic oxidation of gaseous toluene on anatase TiO2 catalyst: Mechanistic aspects and FT-IR investigation

1999

Abstract Photo-oxidation of toluene has been carried out in gas–solid regime by using polycrystalline anatase TiO2 as the catalyst. The reacting gaseous mixture was toluene, air and water in various molar ratios. A pyrex fixed-bed continuous photoreactor irradiated by a medium pressure Hg lamp was used for performing the photoreactivity experiments. The main oxidation product was benzaldehyde but benzene, benzyl alcohol and traces of benzoic acid, phenol and unidentified compounds were also detected. The molar conversion to benzaldehyde with respect to the initial amount of toluene was ca. 20% in the best experimental conditions. Benzene was produced only as a transient product during the f…

AnataseTiO2 (anatase) photocatalystTiO2 (anatase) photocatalyst; Toluene Fourier-transform infrared spectroscopy; Toluene photo-oxidation; Catalysis; Process Chemistry and Technology; Environmental ChemistryToluene photo-oxidationProcess Chemistry and TechnologyInorganic chemistryPhotochemistryTolueneCatalysisCatalysisBenzaldehydeToluene Fourier-transform infrared spectroscopychemistry.chemical_compoundchemistryBenzyl alcoholPhotocatalysisEnvironmental ChemistryBenzeneGeneral Environmental ScienceBenzoic acid
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Determination of fatty alcohol ethoxylates and alkylether sulfates by anionic exchange separation, derivatization with a cyclic anhydride and liquid …

2011

A method for the separation, characterization and determination of fatty alcohol ethoxylates (FAE) and alkylether sulfates (AES) in industrial and environmental samples is described. Separation of the two surfactant classes was achieved in a 50:50 methanol-water medium by retaining AES on a strong anionic exchanger (SAX) whereas most FAE were eluted. After washing the SAX cartridges to remove cations, the residual hydrophobic FAE were eluted by increasing methanol to 80%. Finally, AES were eluted using 80:20 and 95:5 methanol-concentrated aqueous HCl mixtures. Methanol and water were removed from the FAE and AES fractions, and the residues were dissolved in 1,4-dioxane. In this medium, este…

AnionsEthylene OxideFatty alcoholBiochemistryAnalytical ChemistryDioxanesSurface-Active Agentschemistry.chemical_compoundAcetic acidSeawaterDerivatizationChromatography High Pressure LiquidPhthalic anhydrideAqueous solutionChromatographyEsterificationSulfatesElutionOrganic ChemistryExtraction (chemistry)General MedicineChromatography Ion ExchangechemistryMethanolFatty AlcoholsDibenzoxepinsJournal of Chromatography A
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Determination of non-ionic and anionic surfactants in industrial products by separation on a weak ion-exchanger, derivatization and liquid chromatogr…

2013

Abstract A method for the determination of priority surfactants, including fatty alcohol ethoxylates (FAE), alkylether sulfates (AES) and linear alkylbenzene sulfonates (LAS) is described. The samples were diluted with 50% methanol at pH 4 prior to solid-phase extraction on a weak anionic exchanger (WAX). The AES and LAS surfactant classes were retained, whereas the non-ionic components, including most FAE oligomers were eluted. After washing the WAX cartridge to remove cations, the remaining hydrophobic FAE oligomers were eluted using hot 80% methanol at pH 4 (at ca. 50 °C). These two eluates were combined to constitute the non-ionic fraction. Then, AES and LAS were eluted using 80% MeOH w…

AnionsWaxPhthalic anhydrideChromatographyEsterificationLinear alkylbenzeneElutionOrganic ChemistryExtraction (chemistry)Fatty alcoholGeneral MedicineHydrogen-Ion ConcentrationChromatography Ion ExchangeBiochemistryAnalytical ChemistrySurface-Active Agentschemistry.chemical_compoundchemistryvisual_artvisual_art.visual_art_mediumMethanolDerivatizationChromatography High Pressure LiquidJournal of Chromatography A
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Synthesis and biological evaluation of abietic acid derivatives

2009

A series of C18-oxygenated derivatives of abietic acid were synthesized and evaluated for their cytotoxic, antimycotic, and antiviral activities. In general, the introduction of an aldehyde group at C18 did improve the resultant bioactivity, while the presence of an acid or alcohol led to less active compounds.

Antifungal AgentsCarboxylic acidMolecular ConformationAntineoplastic AgentsAlcoholHerpesvirus 1 HumanMicrobial Sensitivity TestsPrimary alcoholAntiviral AgentsChemical synthesisAldehydeStructure-Activity Relationshipchemistry.chemical_compoundChlorocebus aethiopsDrug DiscoveryAnimalsHumansStructure–activity relationshipOrganic chemistryAbietic acidVero CellsCandidaCell ProliferationPharmacologychemistry.chemical_classificationDose-Response Relationship DrugAspergillus fumigatusOrganic Chemistryfood and beveragesStereoisomerismGeneral Medicineequipment and suppliesAspergilluschemistryDrug DesignAbietaneslipids (amino acids peptides and proteins)DiterpeneHeLa CellsEuropean Journal of Medicinal Chemistry
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Alcohol consumption in secondary-school students: effects on plasma total antioxidant capacity

2008

Antioxidant capacityNutrition and DieteticsChemistryMedicine (miscellaneous)Food scienceAlcohol consumptionProceedings of the Nutrition Society
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Wine Consumption and Oral Cavity Cancer: Friend or Foe, Two Faces of Janus

2020

The health benefits of moderate wine consumption have been extensively studied during the last few decades. Some studies have demonstrated protective associations between moderate drinking and several diseases including oral cavity cancer (OCC). However, due to the various adverse effects related to ethanol content, the recommendation of moderate wine consumption has been controversial. The polyphenolic components of wine contribute to its beneficial effects with different biological pathways, including antioxidant, lipid regulating and anti-inflammatory effects. On the other hand, in the oral cavity, ethanol is oxidized to form acetaldehyde, a metabolite with genotoxic properties. This rev…

Antioxidantmedicine.medical_treatmentAnti-Inflammatory AgentsPharmaceutical ScienceReviewresveratrolResveratrolOral cavityAntioxidantsAnalytical Chemistrychemistry.chemical_compound0302 clinical medicineRisk FactorsDrug DiscoveryFood science0303 health sciencesfood and beveragesLipidsReactive Nitrogen SpeciesChemistry (miscellaneous)030220 oncology & carcinogenesisMolecular MedicineMouth NeoplasmscarcinogenesisAlcohol Drinkinglcsh:QD241-44103 medical and health scienceslcsh:Organic chemistrymedicineAnimalsHumanswinePhysical and Theoretical Chemistry030304 developmental biologyConsumption (economics)Winebusiness.industryOrganic Chemistryoral cavity cancerAcetaldehydePolyphenolsCancerDNAmedicine.diseasechemistryEthanol contentethanolReactive Oxygen SpeciesbusinessMutagensacetaldehydeMolecules
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Gas-liquid chromatographic analyses

1983

Abstract The gas chromatography of mixtures of n -alkyl acetates (CH 3 COOR, R = C 1 —C 8 ) and methyl esters of aliphatic n -carboxylic acids (R′COOCH 3 , R′ = C 1 —C 8 ) and certain of their monochlorinated derivatives has been studied on Carbowax 20M and SE-30 glass capillary columns under the same operating conditions. The separation of the isomeric monochlorinated esters was complete on Carbowax 20M, whereas on SE-30 the peaks of 6- and 7-chlorooctyl acetates and methyl (ω − 1)- and (ω − 2)-chlorooctanoates and -nonanoates partly overlapped. The complete separation of the mixtures could not be achieved, however, on Carbowax 20M, in spite of the use of various operating conditions. The …

Aqueous normal-phase chromatographyValeric acidCapillary actionChlorine atomLiquid phasechemistry.chemical_elementAlcoholBiochemistryIsothermal processAnalytical ChemistryHomologous serieschemistry.chemical_compoundChain (algebraic topology)Capillary columnChlorineOrganic chemistryMethyleneChlorine substituentQuartzAlkylchemistry.chemical_classificationPrimary (chemistry)ChromatographyElutionChemistrySubstitution (logic)Organic ChemistryButanoic AcidsReversed-phase chromatographyGeneral MedicineCapillary gas chromatographyChromatographic separationAcyl chainembryonic structuresHalogenNitrocardiovascular systemPolarKovats retention indexGas chromatographyChromatography columnRetention timeGas liquid chromatographicJournal of Chromatography A
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Synthesis of Water-Soluble Copolymers Carrying Long-Chain (C12 to C30 ) Aliphatic Moieties

2011

Water-soluble copolymers from mono-1-alkyl itaconates and N-vinyl-2-pyrrolidone are synthesized and characterized. Themono-1-alkyl itaconates are prepared from itaconic anhydride and the related alcohol: 1-dodecanol, 1-octadecanol, 1-docosanol, and 1-triacontanol. The mono-1-triacontyl itaconate is synthesized fromplant growth regulator policosanols extracted from Agave fourcrouydes, where 1-triacontanol is the major product. The reactivity ratios, calculated according to the Mao-Huglin method for copolymerizations conducted to medium-high conversions, indicate a tendency toward alternation for all copolymerization reactions. Water solubility of copolymers is provided as a function of copol…

Aqueous solutionCopolymer compositionPolymers and PlasticsChemistryOrganic ChemistryRadical polymerizationAlcoholCondensed Matter PhysicsChain lengthchemistry.chemical_compoundWater solublePolymer chemistryMaterials ChemistryCopolymerOrganic chemistryPhysical and Theoretical ChemistryLong chainMacromolecular Chemistry and Physics
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Influence of Phase Modifiers on the Degradation of Tri-n-octylamine/dodecane Extracting Mixture by an Acidic Solution of Vanadium (V)

2012

The kinetics of degradation of a mixture of tri-n-octylamine (extractant) and various alcoholic phase modifiers in n-dodecane in contact with acidic aqueous sulfate solutions containing vanadium (V) has been investigated. The nature of the modifier influences the kinetics of degradation and an improvement of the resistance against the chemical degradation is obtained when secondary alcohol (2-nonanol) or tertiary alcohols such as 9-octyl-9-heptadecanol are used as phase modifiers instead of 1-tridecanol. For instance, the kinetic constant of degradation is divided by one half when 9-octyl-9-heptadecanol is used as phase modifier instead of 1-tridecanol. On the contrary, the alcohols contain…

Aqueous solutionDodecaneGeneral Chemical EngineeringKineticsInorganic chemistryVanadiumchemistry.chemical_elementAlcoholGeneral ChemistrySolventchemistry.chemical_compoundchemistryPhase (matter)Chemical decompositionSolvent Extraction and Ion Exchange
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