Search results for "Photochemical"

showing 10 items of 108 documents

DNA binding, nuclease activity, DNA photocleavage and cytotoxic properties of Cu(II) complexes of N-substituted sulfonamides.

2013

Abstract Ternary copper(II) complexes [Cu(NST)2(phen)] (1) and [Cu(NST)2(NH3)2]·H2O (2) [HNST = N-(4,5-dimethylthiazol-2-yl)naphthalene-1-sulfonamide] were prepared and characterized by physico-chemical techniques. Both 1 and 2 were structurally characterized by X-ray crystallography. The crystal structures show the presence of a distorted square planar CuN4 geometry in which the deprotonated sulfonamide, acting as monodentate ligand, binds to the metal ion through the thiazole N atom. Both complexes present intermolecular π–π stacking interactions between phenanthroline rings (compound 1) and between naphthalene rings (compound 2). The interaction of the complexes with CT DNA was studied b…

DenticityStereochemistryCell SurvivalUltraviolet RaysPhenanthrolineRadicalStackingAscorbic AcidNaphthalenesBiochemistryFluorescence spectroscopyInorganic Chemistrychemistry.chemical_compoundInhibitory Concentration 50Coordination ComplexesCell Line TumorAnimalsHumansDNA CleavageThiazoleNucleaseSulfonamidesBinding SitesbiologyCytotoxinsHydroxyl RadicalDNAHydrogen PeroxidePhotochemical ProcessesKineticschemistrybiology.proteinCattleDNACopperPhenanthrolinesJournal of inorganic biochemistry
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Flow‐Injection Chemiluminescent Determination of Thiamine in Pharmaceutical Samples by On‐line Photodegradation

2004

Abstract A simple, sensitive, and precise method for the determination of thiamine hydrochloride in a flow‐injection system is described. The method is based on the UV irradiation of thiamine in acid medium. Then, the photo‐fragments are oxidized by permanganate in acid medium, and the resultant chemiluminescent intensity is measured. The optimum conditions for the photoreaction and for the chemiluminescence emission were investigated. The method allows the determination of thiamine, over the range 0.05(LOD)–84 mg · l−1, with a throughput of 30 h−1, and a RSD (n, 20) at 20 and 0.5 mg · l−1 of the thiamine level of 2.5 and 1.3%, respectively. The method was applied to pharmaceutical preparat…

Detection limitChromatographyBiochemistry (medical)Clinical BiochemistryThiamine HydrochloridePermanganatefood and beveragesPhotochemistryBiochemistryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundchemistrylawElectrochemistryPhotochemical degradationThiamineIrradiationPhotodegradationhuman activitiesSpectroscopyChemiluminescenceAnalytical Letters
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Keggin heteropolyacid H3PW12O40 supported on different oxides for catalytic and catalytic photo-assisted propene hydration

2013

Catalytic and catalytic photo-assisted hydration of propene to form 2-propanol in gas–solid regime at atmospheric pressure and 85 1C were carried out by using a heteropolyacid (POM) supported on different oxides. Binary materials were prepared by impregnation of H3PW12O40 on different commercial and home prepared supports (TiO2, SiO2, WO3, ZrO2, ZnO, Al2O3). Some of the composites were active both for catalytic and catalytic photo-assisted reactions. The Keggin type POM was completely and partially degraded, when supported on ZnO and Al2O3, respectively, and these binary solids always resulted as inactive for both catalytic and catalytic photo-assisted reactions. The supported Keggin POM sp…

DiffractionDiffuse reflectance infrared fourier transformAtmospheric pressureSurface PropertiesScanning electron microscopeWaterGeneral Physics and AstronomyOxidesAlkenesPhotochemical ProcessesPhotochemistryCatalysisTungstenCatalysisPropenechemistry.chemical_compoundchemistryPressureSettore CHIM/07 - Fondamenti Chimici Delle Tecnologiesense organsIrradiationKeggin heteropolyacid catalytic propene hydration photo-assisted propene hydrationParticle SizePhysical and Theoretical ChemistryFourier transform infrared spectroscopyPhysical Chemistry Chemical Physics
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Screening of physical–chemical methods for removal of organic material, nitrogen and toxicity from low strength landfill leachates

2002

Physical-chemical methods have been suggested for the treatment of low strength municipal landfill leachates. Therefore, applicability of nanofiltration and air stripping were screened in laboratory-scale for the removal of organic matter, ammonia, and toxicity from low strength leachates (NH4-N 74-220 mg/l, chemical oxygen demand (COD) 190-920 mg O2/l, EC50 = 2-17% for Raphidocelis subcapitata). Ozonation was studied as well, but with the emphasis on enhancing biodegradability of leachates. Nanofiltration (25 degrees C) removed 52-66% of COD and 27-50% of ammonia, the latter indicating that ammonia may in part have been present as ammonium salt complexes. Biological pretreatment enhanced t…

Environmental EngineeringChemical PhenomenaNitrogenHealth Toxicology and MutagenesisDaphnia magnaWater Purificationchemistry.chemical_compoundAmmoniaOxidants PhotochemicalOzoneRaphidocelis subcapitataAmmoniaToxicity TestsAnimalsSoil PollutantsEnvironmental ChemistryWater PollutantsAmmoniumAir strippingLeachateOrganic ChemicalsbiologyChemistry PhysicalChemical oxygen demandPublic Health Environmental and Occupational HealthGeneral MedicineGeneral Chemistrybiology.organism_classificationPollutionAcute toxicityRefuse DisposalOxygenDaphniachemistryEnvironmental chemistryFiltrationChemosphere
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Photoinductive efficiency of soil extracted humic and fulvic acids

2002

Humic and fulvic acids extracted from soils of different genesis were investigated for their ability to photoinduce the transformation of fenuron (2 x 10(-4) mol(-1)) at 365 nm. The ratio of the initial rate of fenuron consumption over the rate of light absorption by humic substances was found to be higher for fulvic acids (range 2.0 x 10(-3) to 9.0 x 10(-5)) than for humic acids (range 1.7 x 10(-4) to - 3.6 x 10(-5)). Within the FAs population, this ratio decreased as the specific absorption coefficient at 365 nm increased. It seems therefore that most of 365-nm absorbing components have no photoinductive activity and even reduce that of photoinductive chromophores.

Environmental EngineeringLightPhotochemistryHealth Toxicology and MutagenesisPopulationChemistry Techniques AnalyticalSoilEnvironmental ChemistryHumic acidBenzopyransOrganic mattereducationUltraviolet radiationHumic SubstancesInitial ratechemistry.chemical_classificationeducation.field_of_studyRadiationChromatographyPhenylurea CompoundsPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryPollutionSoil contaminationBiodegradation EnvironmentalchemistryEnvironmental chemistrySoil waterPhotochemical degradationChemosphere
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Features and application of coupled cold plasma and photocatalysis processes for decontamination of water

2020

Dielectric barrier discharge plasma and photocatalysis have been proposed as tools for decontamination of process water, especially in food industry. The present investigation aims to redefine and identify the features of coupling the two technologies in terms of degradation efficiency of a model compound. Results show that, when the process is carried out in plasma activated water in the presence of irradiated TiO2, the efficiency of the integrated process is lower than the sum of the two processes acting separately. It is proposed that afterglow species, e.g. hydrogen peroxide and/or peroxynitrites could be activated by UVA light irradiation producing hydroxyl radicals in the liquid phase…

Environmental EngineeringMaterials sciencePlasma GasesUltraviolet RaysHealth Toxicology and MutagenesisRadical0208 environmental biotechnology2UVA light02 engineering and technologyDielectric barrier discharge010501 environmental sciencesDielectric barrier discharge plasma01 natural sciencesCatalysisWater Purificationchemistry.chemical_compoundphotocatalysiTiOWater decontaminationEnvironmental ChemistryIrradiationFood-Processing IndustryHydrogen peroxide0105 earth and related environmental sciencesTitaniumHydroxyl RadicalPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryHuman decontaminationPlasmaEquipment DesignHydrogen PeroxidePhotochemical ProcessesPollution020801 environmental engineeringMethylene BluechemistryChemical engineeringProcess intensificationPhotocatalysisDegradation (geology)Water Pollutants Chemical
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A survey of photocatalytic materials for environmental remediation

2012

Abstract Heterogeneous photocatalysis is an advanced oxidation process which has been the subject of a huge amount of studies related to air cleaning and water purification. All these processes have been carried out mainly by using TiO 2 -based materials as the photocatalysts and ca. 75% of the articles published in the last 3 years is related to them. This review illustrates the efforts in the search of alternative photocatalysts that are not based on TiO 2 , with some exceptions concerning particularly innovative modifications as nanoassembled TiO 2 or TiO 2 composites with active carbon, graphite and fullerene. Papers reporting preparation, characterization and testing of binary, ternary…

Environmental EngineeringMaterials scienceUltraviolet RaysEnvironmental remediationHealth Toxicology and MutagenesisPortable water purificationNanotechnologyCatalysisEnvironmental ChemistryGraphiteWaste Management and DisposalEnvironmental Restoration and RemediationTitaniumNanotubes CarbonAdvanced oxidation processOxidesMineralization (soil science)Photochemical ProcessesPollutionNanostructuresCharacterization (materials science)Environmental chemistryHeterogeneous photocatalysis photocatalysts not based on TiO2PhotocatalysisEnvironmental PollutantsWater treatmentSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie
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Continuous monitoring of photocatalytic treatment by flow injection. Degradation of dicamba in aqueous TiO2 dispersions

2001

The possible use of flow injection (FI) to monitor the photocatalytic mineralization of dicamba (3,6-dichloro-2-methoxybenzoic acid) present at the trace level in aqueous solutions containing TiO2 suspensions has been evaluated. Experiments were performed in a stirred photochemical reactor equipped with a simple FI manifold, integrating an online filtration unit able to perform the monitoring of the UV absorbance of the irradiated solution every 4 min. The light source used was a medium pressure mercury lamp (125 W). During the initial steps of the reaction the formation of UV absorbing intermediates, which completely disappear in less than 80 min, was evidenced. Additional HPLC, DOC and ch…

Environmental EngineeringPhotochemistryUltraviolet RaysHealth Toxicology and MutagenesisChlorideMineralization (biology)Catalysislaw.inventionOxidants PhotochemicallawmedicineEnvironmental ChemistryIrradiationFiltrationTitaniumAqueous solutionChromatographyHerbicidesChemistryWater PollutionDicambaPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryPollutionPhotocatalysisDegradation (geology)Water treatmentWater Pollutants Chemicalmedicine.drug
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Novel leaf-level measurements of chlorophyll fluorescence for photosynthetic efficiency

2015

Solar induced chlorophyll fluorescence (SIF) from vegetation can now be obtained from satellites as well as ground-based field studies, at select wavelengths associated with atmospheric features. At the leaf level, full spectrum (650–800 nm) chlorophyll emissions (ChlF) can be measured using specialized instrumentation to support interpretation of these SIF observations. We found that ChlF spectra differ for leaf bottoms versus upper leaf surfaces, potentially affecting within-canopy radiative scattering. Our ChlF measurements for leaves of eight tree species (n≥125) obtained during fall 2013 senescence at the Duke Forest in North Carolina, USA and the 2014 growing season (n=72) at the USDA…

Fluorescence Geophysical measurements Indexes Reflectivity Remote sensing Vegetation Vegetation mappingGrowing seasonVegetationPhotosynthetic efficiencyPhotochemical Reflectance Indexchemistry.chemical_compoundHorticultureGEO/10 - GEOFISICA DELLA TERRA SOLIDAchemistryChlorophyllRadiative transferEnvironmental scienceTree speciesChlorophyll fluorescenceRemote sensing
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Iodide-Photocatalyzed Reduction of Carbon Dioxide to Formic Acid with Thiols and Hydrogen Sulfide.

2016

The photolysis of iodide anions promotes the reaction of carbon dioxide with hydrogen sulfide or thiols to quantitatively yield formic acid and sulfur or disulfides. The reaction proceeds in acetonitrile and aqueous solutions, at atmospheric pressure and room temperature by irradiation using a low-pressure mercury lamp. This transition-metal-free photocatalytic process for CO2 capture coupled with H2 S removal may have been relevant as a prebiotic carbon dioxide fixation.

FormatesFormic acidGeneral Chemical EngineeringHydrogen sulfideInorganic chemistryIodidechemistry.chemical_element010402 general chemistryIodine01 natural sciencesCatalysisCatalysisReaccions químiqueschemistry.chemical_compoundEnvironmental ChemistryGeneral Materials ScienceHydrogen SulfideSulfhydryl Compoundschemistry.chemical_classification010405 organic chemistryCarbon fixationCarbon DioxideIodidesPhotochemical ProcessesSulfur0104 chemical sciencesGeneral EnergychemistryCarbon dioxideQuímica orgànicaOxidation-ReductionChemSusChem
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