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DC Field | Value | Language |
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dc.contributor.author | Lal, A. | |
dc.contributor.author | Tan, G. | |
dc.contributor.author | Chai, M. | |
dc.date.accessioned | 2018-03-01T04:20:13Z | - |
dc.date.available | 2018-03-01T04:20:13Z | - |
dc.date.issued | 2008 | |
dc.identifier.uri | http://dspace.uniten.edu.my/jspui/handle/123456789/9509 | - |
dc.description.abstract | A new extraction and cleanup procedure with gas chromatography was developed for the sensitive determination of acephate, dimethoate, malathion, diazinon, quinalphos, chlorpyrifos, profenofos, α-endosulfan, β-endosulfan, chlorothalonil and carbaryl using 1-chloro-4-fluorobenzene as an internal standard in fruits and vegetables. Several extracting and eluting solvents for solid-phase extraction were investigated. The overall extracting solvent with a mixture of acetone:ethyl acetate:hexane (10:80:10, v/v/v) and a eluting solvent of 5% acetone in hexane used with the RPC18 cartridge gave the best recovery for all of the investigated pesticides, and minimized the interference from co-extractants. Under the optimal extraction and clean-up conditions, recoveries of 85 - 99% with RSD < 5.0% (n = 3) for most of the pesticides at the 0.02-0.5 mg/kg level were obtained. The limit of detection was between 0.005-0.01 mg/kg and the limit of quantification was 0.01 mg/kg. This analytical procedure was characterized with high accuracy and acceptable sensitivity to meet requirements for monitoring pesticides in crops. 2008 © The Japan Society for Analytical Chemistry. | |
dc.title | Multiresidue analysis of pesticides in fruits and vegetables using solid-phase extraction and gas chromatographic methods | |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
Appears in Collections: | COE Scholarly Publication |
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