Search results for "Chlorophenol"

showing 10 items of 64 documents

CCDC 921248: Experimental Crystal Structure Determination

2014

Related Article: Ashok Sasmal, Eugenio Garribba, Carlos J. Gómez-García, Cédric Desplanches, Samiran Mitra|2014|Dalton Trans.|43|15958|doi:10.1039/C4DT01699H

(2-(35-Di-t-butyl-2-oxophenylamino)-4-chlorophenolato radical dianion)-(2-(35-di-t-butyl-2-oxophenylamino)-4-chlorophenolato)-cobalt(iii)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 984617: Experimental Crystal Structure Determination

2014

Related Article: Ashok Sasmal, Eugenio Garribba, Carlos J. Gómez-García, Cédric Desplanches, Samiran Mitra|2014|Dalton Trans.|43|15958|doi:10.1039/C4DT01699H

(2-(35-Di-t-butyl-2-oxophenylamino)-4-chlorophenolato radical dianion)-(2-(35-di-t-butyl-2-oxophenylamino)-4-chlorophenolato)-cobalt(iii)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

Successful aerobic bioremediation of groundwater contaminated with higher chlorinated phenols by indigenous degrader bacteria

2018

The xenobiotic priority pollutant pentachlorophenol has been used as a timber preservative in a polychlorophenol bulk synthesis product containing also tetrachlorophenol and trichlorophenol. Highly soluble chlorophenol salts have leaked into groundwater, causing severe contamination of large aquifers. Natural attenuation of higher-chlorinated phenols (HCPs: pentachlorophenol + tetrachlorophenol) at historically polluted sites has been inefficient, but a 4-year full scale in situ biostimulation of a chlorophenol-contaminated aquifer by circulation and re-infiltration of aerated groundwater was remarkably successful: pentachlorophenol decreased from 400 μg L−1 to <1 μg L−1 and tetrachlorophen…

0301 basic medicine246-TRICHLOROPHENOL DEGRADATIONTrichlorophenolDIVERSITYIn situ bioremediation010501 environmental sciences01 natural sciencesbiologinen puhdistusbakteeritBiostimulationchemistry.chemical_compoundQuantitative PCRpentachlorophenol hydroxylaseGroundwaterWaste Management and DisposalPENTACHLOROPHENOLWater Science and Technology2. Zero hungerpcpB geneEcological ModelingIon PGM amplicon sequencingin situ bioremediationContaminationPollutionAerobiosis6. Clean waterBiodegradation EnvironmentalEnvironmental chemistryPentachlorophenol hydroxylaseChlorophenolsEnvironmental Engineeringta1172030106 microbiologySphingomonas sensu latoMICROBIAL-DEGRADATION03 medical and health sciencesBioremediationbioremediationSPHINGOBIUM-CHLOROPHENOLICUMkloorifenolitta219Microbial biodegradationgeneBOREAL GROUNDWATER1172 Environmental sciences0105 earth and related environmental sciencesCivil and Structural EngineeringChlorophenolpohjavesiBacteriaorganic chemicalsion PGM amplicon sequencingSPHINGOMONADSEVOLUTIONPentachlorophenolSOILSchemistryGenes Bacterial13. Climate actionquantitative PCREnvironmental scienceWater Pollutants ChemicalGroundwater
researchProduct

Formation of 2,4,6-trichlorophenol and 2,4,6-trichloroanisole during treatment and distribution of drinking water

1995

Biomethylation of 2,4,6-trichlorophenol to the potent off-flavour compound 2,4,6-trichloroanisole has previously been found to cause taste and odour problems in drinking water. In the present study, both compounds were detected in seemingly unpolluted surface waters. However, the highest concentrations of 2,4,6-trichloroanisole in tap water were caused by the formation of 2,4,6-trichlorophenol during chlorine disinfection of drinking water and subsequent methylation of this compound in the distribution system. Analysis of samples from several sites in the investigated distribution systems showed that there was a substantial spatial and temporal variation of the concentration of both 2,4,6-t…

246-TrichloroanisoleEnvironmental EngineeringOff-flavourchemistry.chemical_elementchemistry.chemical_compoundchemistryTap waterEnvironmental chemistry246-TrichlorophenolChlorineWater treatmentGas chromatographyPhenolsWater Science and TechnologyWater Science and Technology
researchProduct

Solvent dependence of the νs(OD) bandshape in 2,6-dichlorophenol

1994

Abstract The infrared bandshape of νs(OD) of 2,6-dichlorophenol is measured in a series of solvents of increasing polarity, and is quantitatively analysed. The bandshape is described in terms of band indices, moments, correlation functions and correlation times. A distinct solvent dependence of bandshape and relaxation parameters has been found. The changes of the νs(OD) bandshape with increasing solvent polarity are compared in detail with those obtained earlier for analogous solvents for νs(OH) of 2,6-dichlorophenol. The overall behaviour of the spectral and relaxation parameters is similar, but the changes are less distinct for the weaker OD ⋯ Cl bond.

26-DichlorophenolInfraredPolarity (physics)Organic ChemistryRelaxation (NMR)Analytical chemistryInfrared spectroscopyAnalytical ChemistryInorganic ChemistrySolventchemistry.chemical_compoundchemistrySolvent polarityOrganic chemistrySolvent effectsSpectroscopyJournal of Molecular Structure
researchProduct

Kinetics of Cometabolic Biodegradation of 4-Chlorophenol and Phenol by Stenotrophomonas Maltophilia KB2

2018

The cometabolic biodegradation of 4-Chlorophenol (4-CP) by the Stenotrophomonas maltophilia KB2 strain in the presence of phenol (P) was studied. In order to determine the kinetics of biodegradation of both substrates, present alone and in cometabolic systems, a series of tests was carried out in a batch reactor changing, in a wide range, the initial concentration of both substrates. The growth of the tested strain on phenol alone was described by Haldane kinetic model (mm = 0:9 1/h, Ksg = 48:97 gg/m3, KIg = 256:12 gg/m3, Yxg = 0:5715). The rate of 4-CP transformation by resting cells of KB2 strain was also described by Haldane equation and the estimated parameters of the model were: kc = 0…

4-Chlorophenolkineticsphenolcometabolism
researchProduct

Kinetics of cometabolic biodegradation of 4-chlorophenol and phenol by Stenotrophomonas maltophilia KB2

2018

The cometabolic biodegradation of 4-Chlorophenol (4-CP) by the Stenotrophomonas maltophilia KB2 strain in the presence of phenol (P) was studied. In order to determine the kinetics of biodegradation of both substrates, present alone and in cometabolic systems, a series of tests was carried out in a batch reactor changing, in a wide range, the initial concentration of both substrates. The growth of the tested strain on phenol alone was described by Haldane kinetic model (mm=0:9 1/h,Ksg=48:97 gg/m3,KIg=256:12 gg/m3, Yxg=0:5715). The rate of 4-CP transformation by resting cells of KB2 strain was also described by Haldane equation and the estimated parameters of the model were:kc=0:229 gcc =gxh…

4-ChlorophenolkineticsphenolcometabolismChemical and Process Engineering
researchProduct

Assessing the effectiveness of Byssochlamys nivea and Scopulariopsis brumptii in pentachlorophenol removal and biological control of two Phytophthora…

2016

Bioremediation and biological-control by fungi have made tremendous strides in numerous biotechnology applications. The aim of this study was to test Byssochlamys nivea and Scopulariopsis brumptii in sensitivity and degradation to pentachlorophenol (PCP) and in biological-control of Phytophthora cinnamomi and Phytophthora cambivora. B. nivea and S. brumptii were tested in PCP sensitivity and degradation in microbiological media while the experiments of biological-control were carried out in microbiological media and soil. The fungal strains showed low PCP sensitivity at 12.5 and 25 mg PCP L(-1) although the hyphal size, fungal mat, patulin, and spore production decreased with increasing PCP…

Behavior and SystematicPhytophthora0106 biological sciencesPentachlorophenolEvolutionByssochlamysMicrobial Sensitivity TestsPlant Science010501 environmental sciencesPhytophthora cinnamomiFagaceae01 natural sciencesMicrobiologyPatulinchemistry.chemical_compoundOomycetePhytophthora cambivoraGeneticPlant pathogenGeneticsPest Control BiologicalEcology Evolution Behavior and SystematicsPlant Diseases0105 earth and related environmental sciencesByssochlamysEcologybiologyfungiTemperatureFungifood and beveragesbiology.organism_classificationSurvival AnalysisEcology Evolution Behavior and SystematicSporePentachlorophenolPatulinInfectious DiseaseschemistryScopulariopsisScopulariopsisMicrobial InteractionsEnvironmental PollutantsPhytophthoraBioremediationElectrolyte Leakage Assay010606 plant biology & botany
researchProduct

Gas—liquid chromatographic analyses

1984

Abstract The gas chromatography (GC) of n -alkyl acetates (CH 3 COOR), chloroacetates (CH 2 ClCOOR), dichloroacetates (CHCl 2 COOR) and trichloroacetates (CCl 3 COOR), where the alcohol chain length (R) varied between 1 and 8, and certain of their monochlorinated derivatives, 176 compounds altogether, has been studied on SE-30 and OV-351 glass capillary columns under the same operating conditions. The isomeric monochlorinated esters are eluted in direct order from the 1- chloro to the ω-chloro isomer, the separation of the isomers being complete on OV- 351. On SE-30, however, the peaks of the 6- and 7-chlorooctyl esters are partly overlapped. The separation of the mixtures of odd- and e…

Capillary actionAnalytical chemistryAlcoholFormyl groupAldehydeBiochemistryAnalytical Chemistrychemistry.chemical_compoundCapillary columnStraight chainpolycyclic compoundsStructural isomerOrganic chemistryMethyleneBenzoic acidchemistry.chemical_classificationPrimary (chemistry)General MedicineCapillary gas chromatographyBoiling pointChromatographic separationSalicylaldehydeNitrobenzoatesPolarlipids (amino acids peptides and proteins)Aliphatic compoundResolution (mass spectrometry)Polarity (physics)Carboxylic acidchemistry.chemical_elementBranching (polymer chemistry)Isothermal processTurn (biochemistry)ChlorinePhenolsQuartzAlkylTetradecaneChlorophenolDegree of unsaturationChromatographyGeminalElutionOrganic ChemistryChloroacetatesComplete resolutionReverse orderChain lengthchemistryChlorobenzeneFunctional groupNitroKovats retention indexNon polarGas chromatographyVicinalGas liquid chromatographicJournal of Chromatography A
researchProduct

Acute and short-term toxicity of 2,3,4,6-tetrachlorophenol in rats

1981

ChemistryHealth Toxicology and MutagenesisPhysiologyGrowthGeneral MedicineToxicologyPollutionRatsEatingLiverAnimalsShort term toxicityEcotoxicologyTissue DistributionChemical and Drug Induced Liver InjuryChlorophenolsBulletin of Environmental Contamination and Toxicology
researchProduct