Search results for "reaction rate constant"

showing 10 items of 210 documents

EFFICIENT DEGRADATION OF CLOFIBRIC ACID BY HETEROGENEOUS PHOTOCATALYTIC OXIDATION PROCESS

2019

International audience; Emerging pollutants such as pharmaceutical active compounds were detected worldwide in different environmental compartments. Nowadays, multiple studies are focused on the investigation of their environmental fate, as well as to find new, efficient and sustainable removal technologies. Several studies demonstrated that heterogeneous photocatalysis is one of the most promising techniques used for water purification. Thus, the aim of our work was to evaluate the photodegradation efficiency of a refractory emergent compound, named clofibric acid, under UV light in aqueous solution. We report that photodegradation and mineralization efficiency are strongly dependent of th…

Environmental Engineering02 engineering and technology010501 environmental sciencesManagement Monitoring Policy and LawPhotochemistry01 natural sciencesCatalysispersistent micropollutantchemistry.chemical_compoundReaction rate constant[CHIM] Chemical Sciences[CHIM]Chemical Sciencesmineralizationnanosized catalystsPhotodegradation0105 earth and related environmental sciencesdegradationPollutantClofibric acidMineralization (soil science)021001 nanoscience & nanotechnologyPollution6. Clean waterLight intensitychemistry13. Climate actionkineticsPhotocatalysis0210 nano-technologyphotocatalysis
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Über die Stabilität Von Copolymeren aus 1,3,5-Trioxan mit verschiedenen Lactonen

1976

Der thermische Abbau von Copolymeren aus 1,3,5-Trioxan und den Lactonen β-Propiolacton (3-Propanolid), Pivalolacton (2,2-Dimethyl-3-propanolid) und e-Caprolacton (6-Hexanolid) wurde untersucht. Der langsame und vollstandige Abbau der Copolymeren wird zuruckgefuhrt auf 1 eine statistische acidolytische Kettenspaltung durch Carboxyl-Endgruppen, 2 die Abspaltung von Acrylsaure an den sauren Endgruppen, 3 die statistische Kettenspaltung durch Pyrolyse von Esterbindungen vor allem in Sequenzen aus mehreren β-Propiolactonbausteinen. Die Teilreaktionen (1) und (2) konnen durch Zusatz von Butandiol-Diglycidylather-(1,4-Bis(2,3-epoxypropoxy)butan) oder N-(2-Naphthyl)anilin oder von Epoxiden stark ve…

Ethylene oxideChain scissionPolymers and PlasticsChemistrychemistry.chemical_compoundReaction rate constantAnilineColloid and Surface ChemistryButanediolPolymer chemistryCopolymerMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryAcrylic acidColloid and Polymer Science
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Sol–gel material as a support of organometallic catalyst for ethylene polymerization

2008

Abstract The sol–gel procedure was applied to obtain powdery materials with different structures and morphology. It was possible to produce almost non-porous silica powder, with an extremely low surface area (ca. 4 m 2 /g) and very high uniformity of spherical particles as well as materials with various uniformity of particles and different porosity, most likely associated with increasing pore volume. Dependent on the properties of the carrier, the resulting supported vanadium catalysts (VOCl 3 /AlEt 2 Cl) showed significant differences concerning activity and stability. It was confirmed that improved hydrophobicity of the carrier’s surface may be useful and improve the activity of the syst…

Ethylene polymerizationPolymers and PlasticsOrganic ChemistrySupported catalystsGeneral Physics and AstronomyVanadiumchemistry.chemical_elementSilicaPolyethyleneSol–gelChlorideCatalysischemistry.chemical_compoundReaction rate constantchemistryPolymerizationChemical engineeringPolymer chemistryMaterials ChemistrymedicinePorosityPolymerization kineticmedicine.drugSol-gelEuropean Polymer Journal
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Determination of Kinetic and Thermochemical Parameters of a Substitution Reaction at a Square-Planar Palladium(II) Complex in Water/AOT/n-Heptane Mic…

1995

Abstract The substitution reaction [Pd(bipy)(en)] 2+ + en → [Pd(en) 2 ] 2+ + bipy (where bipy = 2,2′-bipyridine and en = ethylenediamine) has been studied in water and water/AOT/ n -heptane microemulsions at various values of the molar ratio R ( R = [water]/[AOT]) by flow microcalorimetry. From calorimetric data, molar enthalpies of reaction and rate constants were obtained. These quantities indicate that, by increasing R , the reaction becomes less exothermic and its rate constant decreases, trending to the value observed in water. These features can be reasonably rationalized in terms of the peculiar solvation state of reactants inside the AOT reversed micelles and/or the peculiar physico…

Exothermic reactionIsothermal microcalorimetryHeptaneChemistryEnthalpySolvationEthylenediamineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryReaction rate constantOrganic chemistryPhysical chemistryMicroemulsionJournal of Colloid and Interface Science
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Bidirectional membrane transport: Simulations of transport inhibition in uptake studies explain data obtained with flavonoids

2006

The purpose of the simulations was to obtain an estimate of concentration-dependent uptake curves when two counteracting transporters are present. On the basis of this experimental data obtained with a pair of ovarian carcinoma cell lines, one of which was not expressing the exsorptive transporter P-glycoprotein and one of which was an MDR1-transfected, P-glycoprotein expressing variant, the kinetics of cellular uptake of the radiolabel (3)H-talinolol were calculated and the inhibitory constants at P-gp were determined for different flavonoids. With respect to the inhibition of P-gp function, among others, naringenin and isoquercitrin were identified as inhibitors, yet estimation of the inh…

Flavonoidschemistry.chemical_classificationNaringeninDose-Response Relationship DrugbiologyFacilitated diffusionFlavonoidKineticsPharmaceutical ScienceBiological TransportTransporterModels TheoreticalMembrane transportPropanolamineschemistry.chemical_compoundReaction rate constantBiochemistrychemistrybiology.proteinAnimalsHumansComputer SimulationATP Binding Cassette Transporter Subfamily B Member 1P-glycoproteinEuropean Journal of Pharmaceutical Sciences
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Disproportionierung und Kombination als Abbruchsmechanismen bei der radikalischen Polymerisation von Styrol, 2. Analyse der temperaturabhängigkeiten

1975

Styrol wurde in Substanz mit 14C-markiertem 2,2′-Azoisobutyronitril im Temperatur-bereich von 30 bis 80°C polymerisiert. Aus der Polymerisationsgeschwindigkeit und der Anzahl der radioaktiven Endgruppen im Polymeren wurden die Effektivitat des Starters f und die Verhaltnisse der Geschwindigkeitskonstanten fur Wachstum, Abbruch und Start k/ka und ka, PR/(kwkst) berechnet. Die Bestimmung der Molekulargewichtsverteilungen mit Hilfe der Gelpermeationschromatographie ermoglichte es, die Ubertragungskonstante CM und das Verhaltnis ka, disp/ka, comb zu berechnen. Die Temperaturabhangigkeiten der Geschwindigkeitskonstanten erwiesen sich als physikalisch sinnvoll. Styrene was bulk polymerised by ini…

Gel permeation chromatographychemistry.chemical_compoundReaction rate constantchemistryPolymerizationTransfer constantPolymer chemistryAtmospheric temperature rangeStyreneDie Makromolekulare Chemie
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Compatibility of surfactants with activated-persulfate for the selective oxidation of PAH in groundwater remediation

2017

Abstract Surfactants foam technology can improve the in situ remediation of hydrophobic organic contaminants by enhancing their solubility and the delivery of remediation chemicals. However, the presence of surfactants may impair the effectiveness of the selective oxidation of those contaminants. To tackle the issue, kinetics and selectivity of phenanthrene (PHE) oxidation in aqueous suspensions and its affecting factors including surfactant concentration (CS) and nature, temperature and persulfate (PS) concentration were studied. Significant differences in selectivity were observed between surfactants, reflecting Coulomb interactions with the anionic oxidizers. Lauryl Betaine (LB) stood ou…

Groundwater remediation02 engineering and technology010501 environmental sciences01 natural sciencesMicellechemistry.chemical_compoundReaction rate constantChemical Engineering (miscellaneous)[CHIM]Chemical SciencesSolubilityWaste Management and DisposalComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciences[SDE.IE]Environmental Sciences/Environmental EngineeringProcess Chemistry and TechnologyPhenanthrene021001 nanoscience & nanotechnologyPersulfatePollution6. Clean waterPhthalic acidchemistry13. Climate actionCritical micelle concentration0210 nano-technologyNuclear chemistry
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Oxidation of melatonin by oxoferryl hemoglobin: A mechanistic study

2002

Reaction of melatonin with the hypervalent iron centre of oxoferryl hemoglobin, produced in aqueous solution from methemoglobin and H2O2, has been investigated at 37 degrees C and pH 7.4, by absorption spectroscopy. The reaction results in reduction of the oxoferryl moiety with formation of a heme-ferric containing hemoprotein. Stopped-flow spectrophotometric measurements provide evidence that the reduction of oxoferryl-Hb by melatonin is first-order in oxoferryl-Hb and first-order in melatonin. The bimolecular reaction constant at pH 7.4 and 37 degrees C is 112 +/- 1.0 M(-1) s(-1). Two major oxidation products from melatonin have been found by gas chromatography-mass spectroscopy: the cycl…

HemeproteinMagnetic Resonance SpectroscopyTime FactorsKynuraminePhotochemistryBiochemistryMethemoglobinGas Chromatography-Mass SpectrometryMelatoninHemoglobinsReaction rate constantmedicineAnimalsMethemoglobinMelatoninIndole testCyclic compoundChemistryOxidesGeneral MedicineHydrogen PeroxideKineticsYield (chemistry)CattleSpectrophotometry UltravioletHemoglobinChlorineOxidation-Reductionmedicine.drug
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Partition Behavior of Anilines in Bulk‐Phase and High‐Performance Liquid Chromatographic Systems: Influence on Correlation with Biological Constants

1992

Abstract The partition behavior of a mixed series of ring‐substituted anilines in reversed‐phase high‐performance liquid chromatographic systems is substantially different from that observed in a classical bulk‐phase partition system with n ‐heptane as the aprotic reference solvent. On the basis of the equivalence of each ring substituent in the p ‐straight‐chain methylene groups (ν value) as a function of the fraction of organic solvent (acetonitrile or methanol) in the mobile phase, the biased partition behavior for imperfect homologues and heterologues is verified relative to that of perfect homologues. This behavior was tentatively attributed, mainly, to differences in the hydrogen bond…

HeptaneAcetonitrilesAniline CompoundsChromatographyChemistryMethanolSubstituentAnalytical chemistryPharmaceutical ScienceIntestinal absorptionSolventPartition coefficientchemistry.chemical_compoundReaction rate constantPartition (number theory)AcetonitrileChromatography High Pressure LiquidJournal of Pharmaceutical Sciences
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Ionic liquids as solvents for the Knoevenagel condensation: understanding the role of solvent–solute interactions

2015

The Knoevenagel condensation in ionic liquids has been demonstrated as a strongly solvent-dependent process. The objective of this study was to establish a simple and descriptive trend of solvent–solute interactions that favour the Knoevenagel condensation in ionic liquid media. The reaction between 4-(dimethylamino)benzaldehyde and ethyl cyanoacetate in several imidazolium- and pyrrolidinium-based ionic liquids and one ionic liquid mixture was studied. The rate constants were rationalised by studying the change in the 1H NMR chemical shift of representative starting materials in the ionic liquids and the measurement and consideration of the Kamlet–Taft descriptors for each solvent. The hyd…

Hydrogen bondChemistryGeneral ChemistryCatalysisSolventBenzaldehydechemistry.chemical_compoundReaction rate constantEthyl cyanoacetateIonic liquidMaterials ChemistryProton NMROrganic chemistryKnoevenagel condensationNew Journal of Chemistry
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