Search results for "Hydroquinone"

showing 10 items of 49 documents

Hybrid TiO2 @ phthalocyanine catalysts in photooxidation of 4-nitrophenol: Effect of the matrix and sensitizer type

2020

Abstract Microcrystalline and nanocrystalline anatase (TiO2) based hybrid photocatalysts including selected phthalocyanine sensitizers were explored in photooxidation of 4-nitrophenol (4-NP) in water. Composites obtained with the homemade pure nano-anatase displayed a very poor catalytic performance compared to the other ones prepared from the commercial Tioxide-Huntsman (micro) and Evonik P25 (nano) products. In particular, the microcrystalline anatase impregnated with sandwich phthalocyanines of Gd or Yb showed excellent results both in photooxidation of 4-NP and hydroquinone, and proved the only ones which completely removed these two compounds from the system during the same reaction cy…

AnataseGeneral Chemical EngineeringHydroquinoneGeneral Physics and Astronomy02 engineering and technology010402 general chemistry01 natural sciences4-nitrophenolCatalysisChemical kineticsReaction ratechemistry.chemical_compoundMetallophthalocyaninesLanthanideLanthanidesHybrid photocatalystHydroquinoneChemistry4-NitrophenolGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesMicrocrystallineChemical engineeringPhthalocyanineTitanium dioxideMetallophthalocyanine0210 nano-technologyHybrid photocatalystsJournal of Photochemistry and Photobiology A: Chemistry
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Nitic oxide promotes strong cytotoxicity of phenolic compounds against escherichia coli. The influence of antioxidant defenses

2003

[EN] The induction of mutagenic and cytotoxic effects by simple phenolics, including catechol (CAT), 3,4dihydroxyphenylacetic acid (DOPAC), hydroquinone (HQ), and 2,5-dihydroxyphenylacetic (homogentisic) acid (HGA), appears to occur through an oxidative mechanism based on the ability of these compounds to undergo autoxidation, leading to quinone formation with the production of reactive oxygen species. This is supported by the detection of such adverse effects in plate assays using Escherichia coli tester strains deficient in the OxyR function, but not in OxyR(+) strains. The OxyR protein is a redox-sensitive regulator of genes encoding antioxidant enzymes including catalase and alkyl hydro…

AntioxidantUltraviolet Raysmedicine.medical_treatmentCatecholsOxidative toxicityFree radicalsOxidative phosphorylationNitric OxideBiochemistryAntioxidantschemistry.chemical_compoundCaffeic AcidsQUIMICA ORGANICASuperoxidesPhysiology (medical)medicineEscherichia coliBIOQUIMICA Y BIOLOGIA MOLECULARHydrogen peroxidechemistry.chemical_classificationMelaninsReactive oxygen speciesbiologyHydroquinoneAutoxidationDose-Response Relationship DrugPhenolEscherichia coli ProteinsNitric oxideHydrogen PeroxideCatalaseFlow CytometryQuinoneHydroquinonesDNA-Binding ProteinsOxygenRepressor ProteinschemistryBiochemistryCatalaseMutationbiology.proteinQuinoneOxyROxidation-ReductionDNA DamageMutagensTranscription Factors
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Photocatalytic degradation of toluene in aqueous suspensions of polycrystalline TiO2 in the presence of the surfactant tetradecyldimethylamino-oxide

2000

The heterogeneous photocatalytic method has been used for carrying out the toluene oxidation in synthetic aqueous solutions containing also a zwitterionic surfactant, i.e. tetradecyldimethylamino-oxide (C 14 DMAO). A batch photoreactor with immersed lamp and two kinds of polycrystalline TiO 2 catalysts were used. The results indicate a substantial increase of the toluene degradation rate in the presence of the surfactant; the complete photo- oxidation of toluene was achieved in a few hours of irradiation at the used experimental conditions; at higher irradiation times also C 14 DMAO was completely degraded. The main intermediates of toluene degradation were p-cresol (4-methyiphenol) and ben…

Benzaldehydechemistry.chemical_compoundMuconic acidchemistryHydroquinoneBenzyl alcoholPhotocatalysisPhotochemistryTolueneToluene oxidationBenzoic acid
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Effects of marine 2-polyprenyl-1,4-hydroquinones on phospholipase A2 activity and some inflammatory responses.

1995

Three 2-polyprenyl-1,4-hydroquinone derivatives (2-heptaprenyl-1,4-hydroquinone: IS1, 2-octaprenyl-1,4-hydroquinone: IS2 and 2-[24-hydroxy]-octaprenyl-1,4-hydroquinone: IS3) isolated from the Mediterranean sponge Ircinia spinosula, were evaluated for effects on phospholipase A2 activity of different origin (Naja naja venom, human recombinant synovial fluid and bee venom), as well as on human neutrophil function and mouse ear oedema induced by 12-O-tetradecanoylphorbol 13-acetate (TPA). IS1 interacted minimally with these responses. In contrast, IS2 and IS3 inhibited human recombinant synovial phospholipase A2 in a concentration-dependent manner, with minor effects on the rest of the enzymes…

Blood PlateletsLeukocyte migrationLeukotriene B4Cell SurvivalNeutrophilsPharmacologyBiologyIn Vitro TechniquesLeukotriene B4Phospholipases Achemistry.chemical_compoundMicePhospholipase A2SuperoxidesMicrosomesSynovial fluidAnimalsEdemaHumansPharmacologyPhospholipase AL-Lactate DehydrogenasePancreatic ElastaseAnti-Inflammatory Agents Non-SteroidalDegranulationBiological activityHydroquinonesPoriferaThromboxane B2Thromboxane B2Phospholipases A2Biochemistrychemistrybiology.proteinTetradecanoylphorbol AcetateEuropean journal of pharmacology
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Isoprenylhydroquinone glucoside: a new non-antioxidant inhibitor of peroxynitrite-mediated tyrosine nitration

2004

Abstract Three hydroquinone glucosides and four caffeoylquinic esters were examined for their effect on tyrosine nitration, as well as on the oxidation of dihydrorhodamine (DHR) 123 and cytochrome c 2+ induced by peroxynitrite. All these phenolics, which had previously been characterized as the active principles of the plant Phagnalon rupestre , were fairly active in preventing the oxidation of DHR 123, though inefficient in the cytochrome c test. While their antioxidant potency is associated with the presence of a caffeoyl moiety, not so an obvious chemical character was correlated to a greater activity against nitration of tyrosine. Here, the highest potency corresponded to 2-isoprenylhyd…

Cancer ResearchAntioxidantCytochromePhysiologymedicine.medical_treatmentClinical BiochemistryAsteraceaeBiochemistrychemistry.chemical_compoundGlucosidesGlucosidePeroxynitrous AcidNitrationmedicineTyrosineNitratesMolecular StructurebiologyHydroquinoneRhodaminesCytochrome cCytochromes cHydroquinoneschemistryBiochemistrybiology.proteinTyrosineOxidation-ReductionPeroxynitriteNitric Oxide
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Determination of hydroquinone and metal in photographic developer by reversed-phase ion-pair chromatography with amperometric detection

1988

Abstract Sodium 1-heptanesulphonate is used as an ion-pair reagent for the chromatographic separation of the two developing agents on a phenylsilica micro-column, with amperometric detection at an applied potential of + 0.75 V (vs. Ag/AgCl). No pretreatment of the developer is necessary. Linear calibration graphs were obtained in the range 10 −5 -1.5 × 10 −4 M.

ChromatographyHydroquinoneChemistrySodiumIon chromatographychemistry.chemical_elementReversed-phase chromatographyBiochemistryAmperometryPhotographic developerAnalytical ChemistryMetalchemistry.chemical_compoundvisual_artReagentvisual_art.visual_art_mediumEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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A tandem-flow assembly for the chemiluminometric determination of hydroquinone

2003

A direct chemiluminescent procedure for determination of hydroquinone based on the emergent flow methodology known as multicommutation or tandem-flow is presented for first time. The manifold was based on a set of three channels and three solenoid valves; and, the determination was performed at 60degreesC and at flow-rate of 7.5 ml min(-1). The complete cycle lasted 35 s, which resulted in a sample flow trough of 103 h(-1). The chemical process was the hydroquinone oxidation with the system sulphuric acid-potassium permanganate; and the light emission was clearly enhanced by the presence of quinine sulphate and benzalkonium chloride reaching a detection limit of 30 Rg l(-1). The dynamic int…

Detection limitChemiluminescenceChromatographyHydroquinoneHydroquinonePermanganateAnalytical chemistrySulfuric acidAnalytical Chemistrylaw.inventionchemistry.chemical_compoundBenzalkonium chloridePotassium permanganatechemistryEnvironmental sampleslawTandem-flowQUIMICA ANALITICAmedicinePharmaceuticalsLight emissionChemiluminescencemedicine.drugTalanta
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Temperature dependence of the isotropic hyperfine coupling constants in 1,4-hydroquinone and 1,4-dihydroxynaphthalene cation radicals

1998

Electron paramagnetic resonance spectroscopyHyperfine couplingchemistry.chemical_compoundHydroquinoneChemistryComputational chemistryRadicalIsotropyPhysical chemistryGeneral Materials ScienceGeneral ChemistryMagnetic Resonance in Chemistry
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Studies on pathways of ring opening of benzene in a Fenton system

1995

Ring-opened products of benzene metabolism have been postulated to play a role in hematotoxicity and leukemogenesis. The reaction of benzene in the Fenton system was reexamined to determine the presence of compounds which might serve as intermediates in the formation of trans, trans-muconaldehyde (MUC), a microsomal hematotoxic metabolite of benzene. Benzene dihydrodiol (DHD) was found in this system based on coelution with authentic standard, ultraviolet (UV) absorption characteristics, and molecular weight. Incubation of DHD in the Fenton system resulted in the formation of phenol (PH), catechol (CAT), and products which reacted with thiobarbituric acid to form chromogens absorbing at 495…

Free RadicalsStereochemistryMetaboliteStereoisomerismIn Vitro TechniquesBiochemistryAldehydechemistry.chemical_compoundPhysiology (medical)AnimalsHumansPhenolBenzeneChromatography High Pressure LiquidCarcinogenchemistry.chemical_classificationAldehydesCatecholMolecular StructureHydroquinoneBenzeneStereoisomerismchemistrySpectrophotometryCarcinogensMicrosomes LiverFree Radical Biology and Medicine
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Electrochemical performance of activated screen printed carbon electrodes for hydrogen peroxide and phenol derivatives sensing

2019

Screen-printed carbon electrodes (SPCEs) are widely used for the electroanalysis of a plethora of organic and inorganic compounds. These devices offer unique properties to address electroanalytical chemistry challenges and can successfully compete in numerous aspects with conventional carbon-based electrodes. However, heterogeneous kinetics on SPCEs surfaces is comparatively sluggish, which is why the electrochemical activation of inks is sometimes required to improve electron transfer rates and to enhance sensing performance. In this work, SPCEs were subjected to different electrochemical activation methods and the response to H2O2 electroanalysis was used as a testing probe. Changes in to…

General Chemical EngineeringElectrochemical activationchemistry.chemical_element02 engineering and technology010402 general chemistryElectrochemistry01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundElectrochemistryQuímica FísicaScreen-printed carbon electrodesSensorHydroquinoneSulfuric acidChronoamperometryHydrogen peroxide021001 nanoscience & nanotechnologyPhenolic compounds0104 chemical sciencesDielectric spectroscopychemistryChemical engineeringElectrodeSurface modificationCyclic voltammetry0210 nano-technologyCarbonJournal of Electroanalytical Chemistry
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