Search results for "Reaction pathway"

showing 5 items of 5 documents

Comparative electrochemical treatments of two chlorinated aliphatic hydrocarbons. Time course of the main reaction by-products.

2011

The chlorinated aliphatic hydrocarbons conjugate toxicity with high chemical stability, bioaccumulation and long-range diffusivity. Chloroethanes are particularly ubiquitous in the industry and in household products, and their entry to the environment may entail potential risks for the living beings. At present, the US Environmental Protection Agency is carrying out the Endocrine Disruptor Screening Program (EDSP), where 1,2-dichloroethane (DCA) and 1,1,2,2-tetrachloroethane (TCA) are considered as priorities for their potential effects on the endocrine system. DCA is also found in the list of priority substances drawn up by the European Commission. To avoid the release of chloroethanes int…

Environmental EngineeringTime FactorsFormic acidHealth Toxicology and MutagenesisOxalic acidInorganic chemistryReaction pathway1122-Tetrachloroethanechemistry.chemical_element12-DichloroethaneAcetatesElectrochemistryOrganochlorinated pollutant1122-Tetrachloroethane.Chemistry Techniques AnalyticalDiffusionchemistry.chemical_compound12-DichloroethaneElectrochemical water treatment technologieOxidizing agentChlorineElectrochemistryHydrocarbons ChlorinatedEnvironmental ChemistryEthylene DichloridesWaste Management and DisposalElectrodesEthaneAqueous solutionDichloroacetic Acid1122-TetrachloroethaneEquipment DesignHydrogen PeroxidePollutionOxygenchemistryElectro-FentonChlorineJournal of hazardous materials
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Ruthenium‐assisted tellurium abstraction in bis(thiophen‐2‐yl) ditelluride

2023

The reaction of [RuCl2(CO)3]2 and Te2Tpn2 (Tpn = thiophen-2-yl, C4H3S) in the absence of light resulted in the formation of cct-[RuCl2(CO)2(TeTpn2)2] (1) [cis(Cl)-cis(CO)-trans(TeTpn2)] and TeTpn2 (2) together with the precipitation of tellurium. The complex 1 and the monotelluride 2 were characterized by NMR spectroscopy and single-crystal X-ray diffraction. The decomposition of Te2Tpn2 to TeTpn2 has been monitored by 125Te NMR spectroscopy and seemed to be faster than the ligand substitution in [RuCl2(CO)3]2 by TeTpn2. A catalytic cycle is proposed for the decomposition of Te2Tpn2 to TeTpn2 based on the PBE0-D3/def2-TZVP calculations. peerReviewed

Inorganic Chemistrycrystal structurestelluuriBis(thiophen-2-yl) ditellanedicarbonyldichloridobis[bis(thiophen-2-yl)tellane]rutheniumreaction pathwaykompleksiyhdisteetorganometalliyhdisteettellurium abstraction
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Partial photocatalytic oxidation of glycerol in TiO2 water suspensions

2010

2nd European Conference on Environmental Applications of Advanced Oxidation Processes -- SEP 09-11, 2009 -- Nicosia, CYPRUS

Settore ING-IND/24 - Principi Di Ingegneria ChimicaAnataseTitanium DioxideAqueous solutionFormic acidElectrospray ionizationGlycerol partial oxidation Selective photocatalytic oxidation Titanium dioxide Reaction pathwaysInorganic chemistryAqueous two-phase systemGeneral ChemistryCatalysischemistry.chemical_compoundchemistryGlyceraldehydeTitanium dioxideGlycerolSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSelective Photocatalytic OxidationGlycerol Partial OxidationReaction Pathways
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Selective oxidation of phenol and benzoic acid in water via home-prepared TiO2 photocatalysts: Distribution of hydroxylation products

2012

Abstract The hydroxylation of phenol (a substrate containing an electron donor group) and of benzoic acid (a substrate containing an electron withdrawing group) has been carried out by the photocatalytic method in aqueous suspensions containing commercial or home prepared TiO2 samples. The aim of the work was to study the distribution of hydroxylation products when different photocatalysts were used and to correlate the selectivity to some physico-chemical features of the powders. The samples were characterized by X-ray diffraction, thermogravimetry, determination of crystalline phase percentage, specific surface area and zero charge point. The photoreactivity results indicate that the prod…

Settore ING-IND/24 - Principi Di Ingegneria ChimicaProcess Chemistry and TechnologyInorganic chemistryElectron donorCatalysisCatalysisHydroxylationchemistry.chemical_compoundchemistrySelective hydroxylation Product distribution Benzoic acid Phenol Heterogeneous photocatalysis Reaction pathways Kinetics TiO2PhotocatalysisPhenolPartial oxidationSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSelectivityBenzoic acid
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Photocatalytic oxidation of nitrobenzene and phenylamine: Pathways and kinetics

2007

WOS: 000245150800018

Settore ING-IND/24 - Principi Di Ingegneria ChimicaReaction mechanismEnvironmental EngineeringAqueous solutionPartial oxidation nitrobenzene phenylamine heterogeneous photocatalysis reaction pathway kinetics TiOGeneral Chemical EngineeringNitrobenzeneKineticsInorganic chemistryPartial OxidationHeterogeneous PhotocatalysisMineralization (soil science)PhotochemistryReaction PathwayNitrobenzeneKineticschemistry.chemical_compoundAdsorptionchemistryPhotocatalysisTio2Partial oxidationPhenylamineBiotechnologyAIChE Journal
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