about
Biological activities of extracts from sumac (Rhus spp.): a review.Mechanistic aspects regarding the direct aqueous environmental photochemistry of phenol and its simple halogenated derivatives. A review.Perfluoroalkyl sulfonic and carboxylic acids: a critical review of physicochemical properties, levels and patterns in waters and wastewaters, and treatment methods.Evidence for increasingly variable Palmer Drought Severity Index in the United States since 1895.Dow and Kaw,eff vs. Kow and Kaw degrees: acid/base ionization effects on partitioning properties and screening commercial chemicals for long-range transport and bioaccumulation potential.Estimated congener specific gas-phase atmospheric behavior and fractionation of perfluoroalkyl compounds: rates of reaction with atmospheric oxidants, air-water partitioning, and wet/dry deposition lifetimes.Congener-specific numbering systems for the environmentally relevant C4 through C8 perfluorinated homologue groups of alkyl sulfonates, carboxylates, telomer alcohols, olefins, and acids, and their derivatives.Comment on "Important role of reaction field in photodegradation of deca-bromodiphenyl ether: Theoretical and experimental investigations of solvent effects" by Q. Xie, J. Chen, J. Shao, C. Chen, H. Zhao, C. Hao [Chemosphere 76(11) (2009) 1486-1490]Modeling the hydrolysis of perfluorinated compounds containing carboxylic and phosphoric acid ester functions and sulfonamide groups.Quantitative structure-activity relationship (QSAR) studies for predicting activation of the ryanodine receptor type 1 channel complex (RyR1) by polychlorinated biphenyl (PCB) congeners.A new class of perfluorinated acid contaminants: primary and secondary substituted perfluoroalkyl sulfonamides are acidic at environmentally and toxicologically relevant pH values.Congener-specific organic carbon-normalized soil and sediment-water partitioning coefficients for the C1 through C8 perfluoroalkyl carboxylic and sulfonic acids.Comment on "Photodegradation pathways of nonabrominated diphenyl ethers, 2-ethylhexyltetrabromobenzoate and di(2-ethylhexyl)tetrabromophthalate: identifying potential markers of photodegradation".Comment on "Comparative assessment of the global fate and transport pathways of long-chain perfluorocarboxylic acids (PFCAs) and perfluorocarboxylates (PFCs) emitted from direct sources".Comment on "Linear and branched perfluorooctane sulfonate isomers in technical product and environmental samples by in-port derivatization-gas chromatography-mass spectrometry".Comment on "Ab initio study of the structural, electronic, and thermodynamic properties of linear perfluorooctane sulfonate (PFOS) and its branched isomers" by F.J. Torres, V. Ochoa-Herrera, P. Blowers, R. Sierra-Alvarez [Chemosphere 76 (8) (2009) 1Thermodynamic properties of chloramine formation and related reactions during water treatment: a G4MP2, G4, and W1BD theoretical study.Evidence for tin inhibition of enhanced biological phosphorus removal at a municipal wastewater treatment plant.Comment on "degradation of organic molecules in advanced oxidation processes: relation between chemical structure and degradability [Chemosphere 91 (2013) 383-389]".Comment on "In situ air-water and particle-water partitioning of perfluorocarboxylic acids, perfluorosulfonic acids and perfluorooctyl sulfonamide at a wastewater treatment plant [Vierke et al. Chemosphere 2013 doi:10.1016/j.chemosphere.2013.02.067]Comment on Screening for PBT chemicals among the "existing" and "new" chemicals of the EU.Comment on "Partitioning of polar and non-polar neutral organic chemicals into human and cow milk [Geisler et al., Environ Int 2011; 37: 1253-1258]".Comment on "A computational study on enzymatically driven oxidative coupling of chlorophenols: an indirect dehalogenation reaction [Szatkowski and Dybala-Defratyka, Chemosphere 91 (2013) 258-264]".Comment on "potential carcinogenic hazards of non-regulated disinfection by-products: Haloquinones, halo-cyclopentene and cyclohexene derivatives, N-halamines, halonitriles, and heterocyclic amines (Bull et al., 2011. Toxicology 286, 1-19)".Comment on "Prediction of soil sorption coefficients using model molecular structures for organic matter and the quantum mechanical COSMO-SAC model".Occurrence and congener profiles of polybrominated diphenyl ethers (PBDEs) in environmental samples from coastal British Columbia, Canada.Exponential increases of the brominated flame retardants, polybrominated diphenyl ethers, in the Canadian Arctic from 1981 to 2000.Photochemical mass balance of 2,3,7,8-TeCDD in aqueous solution under UV light shows formation of chlorinated dihydroxybiphenyls, phenoxyphenols, and dechlorination products.Estimated bioconcentration factors (BCFs) for the C(4) through C(8) perfluorinated alkylsulfonic acid (PFSA) and alkylcarboxylic acid (PFCA) congeners.Comment on "photolysis of Enrofloxacin in aqueous systems under simulated sunlight irradiation: kinetics, mechanism and toxicity of photolysis products [Li et al., Chemosphere 85 (2011) 892-897]".Anaerobic microbial and photochemical degradation of 4,4'-dibromodiphenyl ether.Comment on Stilbene levels in grape cane of different cultivars in southern Chile: determination by HPLC-DAD-MS/MS method.Comment on "Identification of substances with potential for long-range transport as possible substances of very high concern [Zarfl et al., Environ Sci Pollut Res (2012) 19:3152-3161]".Comment on "QSPR modeling of bioconcentration factor of nonionic compounds using Gaussian processes and theoretical descriptors derived from electrostatic potentials on molecular surface [Peng et al. Chemosphere 83 (2011) 1045-1052]".Comment on "Targeting aquatic microcontaminants for monitoring: exposure categorization and application to the Swiss situation [Gotz et al., Environ Sci Pollut Res (2010) 17:341-354]".Comment on "Atmospheric degradation of perfluoro-2-methyl-3-pentanone: photolysis, hydrolysis, and hydration".Comment on "Development of a magnetic particle immunoassay for polybrominated diphenyl ethers and application to environmental and food matrices" by Weilin L. Shelver et al. [Chemosphere 73 (1S) (2008) S18-S23].Comment on "specific binding of hydroxylated polychlorinated biphenyl metabolites and other substances to bovine calf uterine estrogen receptor: structure-binding relationships [Kramer and Giesy, Sci Total Environ 1999;233:141-61]".Photochemical rearrangement of dibenzo[1,4]dioxins proceeds through reactive spirocyclohexadienone and biphenylquinone intermediates.Using exterior building surface films to assess human exposure and health risks from PCDD/Fs in New York City, USA, after the World Trade Center attacks.
P50
Q36957612-EBC93F30-015F-45E1-B806-EF731DDA4A8BQ37302366-0B19209E-8007-46A2-B699-DC066F24EAB9Q37619332-147C50FC-F6BC-4443-AD7E-8CFED0EFAC65Q39387482-646B656E-BDC2-4815-9174-E9E029BFE546Q39846192-5E1297CA-B26F-4272-A43A-02125562C752Q39938786-F1745322-B19F-4EA3-BB74-FE44695DEEBCQ40049424-C0B9C202-BDD1-4F4C-AF26-8749C5ECA36AQ43004383-FB26BF9D-9926-49DB-B19F-EF42F8EBA0C8Q43100266-975C0AFF-720E-441F-A1B6-C84261B62464Q43100278-499517E8-9B9A-4C13-876C-BB8E4C29958DQ43150315-32D536DB-1352-4345-95D5-ECA1CFE6838CQ43150318-C4D234F8-1131-4D47-A4C2-B0419117F62EQ43239671-FA495BD2-3A7C-4AA8-8377-5C92D5E45408Q43266550-059606A2-9948-4C6D-BC5F-B4EBF3E70989Q43290872-53B4C1E7-55F3-4A4A-A465-E7CED59F9513Q43295476-5399DC46-E668-46B5-BFC4-9FA80209D6A8Q43315116-C3784CD4-CE8F-46C2-A49D-AE745A0AA264Q43319885-06E91554-C7E4-419B-AD49-E4FA1CED7B3BQ43359381-5AA0123B-B66A-436C-94C9-06EFD4B65DEBQ43360287-839A1DE1-44AC-4001-959A-1DC4B067FD4AQ43599854-C41ECC41-D67C-410D-A0D0-F8F875D565AFQ43779718-8535F1E3-AE28-4FD5-AF91-90891C318F7EQ43820563-BD79F596-4B4B-42DE-9FFF-50DF43417779Q43872058-A4F955D8-134D-4FB6-9F69-C9FB1D01E9A1Q43888749-8728FD8D-3B71-4307-BEF6-78364589C02EQ43985973-E384BA87-93E6-429D-950F-21644A960533Q44003671-65E25DB9-14F4-4C7E-B7C8-2D5FFE6C5D63Q44003692-091A0616-6EC1-4DBD-BF63-E19A08AB29F5Q44037675-E857D71B-29A5-455C-869F-FAE8024B0D5BQ44301376-0210B80C-2969-4CF9-A314-E34FFA5CFA10Q44399193-5A9E498B-24AB-46C8-AA45-7FC612CC3F21Q44523265-CE21F030-7AE9-4C83-9A87-36F4A7FA6BAEQ44606594-BEE6F307-8A73-4A9A-8F4D-94AF6710A837Q45150079-51FA1783-498F-4E43-99CD-C30DDE2A3971Q45733217-6922C4FF-BA66-48AE-87C2-A38BF523672CQ45779807-D419883B-564B-4908-9873-707120F66050Q46376040-D291C540-ECDE-4013-9F16-FA5711D01020Q46775825-026145BE-8044-4468-AA6E-AE1F205AA64EQ46776496-F7E94E38-3643-41D4-9B47-D55F39453D8EQ46824974-A383E389-229D-46E6-A795-B78E0A20E59B
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Sierra Rayne
@ast
Sierra Rayne
@en
Sierra Rayne
@es
Sierra Rayne
@nl
Sierra Rayne
@sl
type
label
Sierra Rayne
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Sierra Rayne
@en
Sierra Rayne
@es
Sierra Rayne
@nl
Sierra Rayne
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prefLabel
Sierra Rayne
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Sierra Rayne
@en
Sierra Rayne
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Sierra Rayne
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Sierra Rayne
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P1053
N-5973-2015
P106
P1153
6603400010
P31
P3829
P496
0000-0001-9094-0909