Results 171 to 180 of about 8,389 (210)
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Kinetics of aqueous base and acid hydrolysis of aldicarb, aldicarb sulfoxide and aldicarb sulfone

Journal of Environmental Science and Health, Part B, 1983
The kinetics of degradation of aqueous solutions of aldicarb, aldicarb sulfoxide and aldicarb sul fone by base hydrolysis were investigated. Pseudo first order rate constants of 37 micrograms/l solutions were determined at different hydroxide concentrations by acid-base titration.
A T, Lemley, W Z, Zhong
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Determination of aldicarb, aldicarb oxime, and aldicarb nitrile in water by gas chromatography/mass spectrometry

Analytical Chemistry, 1984
Limites de detection: 0,3-1,2 et 0,15 ng, respectivement pour l'aldicarb et ses deux produits de degradation oxime et ...
Michael L. Trehy   +2 more
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Separation of aldicarb, aldicarb sulfoxide, and aldicarb sulfone on unmodified silica with reverse-phase eluents

Chromatographia, 1987
Aldicarb, aldicarb sulfoxide, and aldicarb sulfone were chromatographed on an octyl-silica bonded-phase column and on an unmodified silica column using acetonitrile/water mobile phases. The elution order of the analytes from the silica column was different from that using the octyl-silica bonded phase and allowed confirmation of residues of aldicarb ...
C. J. Miles, H. A. Moye
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Toxicology of Aldicarb

1988
Aldicarb (2-methyl-2[methylthio]propionaldehyde 0-[methyl carbamoyl]-oxime; TEMIK®, Rhone-Poilenc’s registered trademark) effectively controls a wide variety of insects, mites, and nematodes and is used worldwide on more than 40 economically important crops.
R L, Baron, T L, Merriam
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Hydrolysis of aldicarb, aldicarb sulfoxide, and aldicarb sulfone at parts per billion levels in aqueous media

Journal of Agricultural and Food Chemistry, 1984
On etudie les taux de degradation de l'aldicarbe, de son sulfoxyde et de sa sulfone en solution aqueuse dans le contexte d'une etude systematique sur les methodes de detoxication des carbamates dans l'eau ...
Ann T. Lemley, Wei Z. Zhong
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Degradation of aldicarb, aldicarb sulfoxide, and aldicarb sulfone in chlorinated water

Environmental Science & Technology, 1991
The three insecticidal species of Temik, aldicarb (I), aldicarb sulfoxide (II), and aldicarb sulfone (III), degrade rapidly in chlorinated water. I is sulfoxidized to II, while II forms III, (chloromethyl)sulfonyl species, and N-chloro-II. III forms N-chloro-III, which decomposes to III acid and dichloromethylamine.
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Determination of aldicarb, aldicarb sulfoxide, aldicarb sulfone and carbofuran residues in water using high-performance liquid chromatography

Journal of Chromatography A, 1982
Abstract A method was developed for the residue analysis of aldicarb, its toxic metabolites (aldicarb sulfoxide and aldicarb sulfone), carbofuran and its metabolites (3-hydroxy- and 3-ketocarbofuran) in water. The procedure involved extracting with methylene chloride, initial separation and clean-up with a Sep-PakTM silica cartridge, followed by high-
W.P. Cochrane, M. Lanouette, S. Trudeau
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Aldicarb Contamination of Groundwater

1988
Aldicarb, [2-methyl-2-(methylthio)propionaldehyde O-(methylcarbamoy1)-oxime], the active ingredient in TEMIK® insecticide/nematicide, was discovered in 1962 (Weiden et al. 1965) and is currently registered in over 60 countries for a large number of crops.
H A, Moye, C J, Miles
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Development and evaluation of a magnetic particle based enzyme immunoassay for aldicarb, aldicarb sulfone and aldicarb sulfoxide

Chemosphere, 1992
Abstract A magnetic particle based solid-phase enzyme linked immunosorbent assay (ELISA) for the determination of parts per billion levels of aldicarb and its sulfoxide and sulfone metabolites in water was developed. Sensitivity is estimated at 250 ppt based on a 90% B/Bo with results available in less than one hour. Photometric analysis of the final
Jeanne A. Itak   +2 more
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Transformation of aldicarb sulfoxide and aldicarb sulfone in four water‐saturated sandy subsoils

Pesticide Science, 1995
AbstractThe transformation of aldicarb sulfoxide and aldicarb sulfone was studied in incubations with water‐saturated subsoils under simulated field conditions at 10°C. The subsoils were collected at four locations from beneath the water table at a depth of 2.5 to 3.5 m.
Smelt, J.H.   +2 more
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