1999
DOI: 10.1007/s002160051270
|View full text |Cite
|
Sign up to set email alerts
|

Determination of organophosphorus pesticides in soil by headspace solid-phase microextraction

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
11
0
1

Year Published

2002
2002
2016
2016

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 61 publications
(12 citation statements)
references
References 0 publications
0
11
0
1
Order By: Relevance
“…Therefore, we considered HS-SPME as an alternative to DI-SPME. HS-SPME has been applied to the determination of semi-volatile organophosphorus pesticides in soil by Ng et al [32]. Considering the physico-chemical characteristics of analytes, as regards volatility, the headspace mode seems to be an attractive alternative to direct immersion.…”
Section: Spme Optimisationmentioning
confidence: 99%
“…Therefore, we considered HS-SPME as an alternative to DI-SPME. HS-SPME has been applied to the determination of semi-volatile organophosphorus pesticides in soil by Ng et al [32]. Considering the physico-chemical characteristics of analytes, as regards volatility, the headspace mode seems to be an attractive alternative to direct immersion.…”
Section: Spme Optimisationmentioning
confidence: 99%
“…It is the most common organophosphate insecticide applied in the United States [12]. Various methodologies such as LLE-GC, SPE-GC, cloud-point extraction-LC-UV and SPME-GC have been employed to analyze malathion [13][14][15][16][17][18].…”
Section: Introductionmentioning
confidence: 99%
“…SPME is now considered to be a fairly mature sample-preparation technique with wide applications for the determination of polar and non-polar pollutants in water samples ranging from environmental, biomedical to agricultural; the technique has been used to a host of scientific and industrial important samples by various researchers including the analysis of pesticides [4], PAHs [5], substituted benzene compounds [6] and trihalomethanes [7] in aqueous samples. It is a solventfree process that combines sampling, extraction, concentration and instrument introduction into a single step; it successfully overcomes the inherent shortcomings of conventional and complicated sample-preparation methods described previously [8][9][10]. However, it has a few drawbacks, such as limited lifetime and linear range, fragility of the fibers, lower extraction efficiency, sample carryover, relatively expensive fibers and fiber assembly holder [11].…”
Section: Introductionmentioning
confidence: 99%