AI Article Synopsis

  • Trichlorfon can catalyze the oxidation of benzidine to produce 4-amino-4'-nitro biphenyl when combined with sodium perborate, which was confirmed through LC-MS analysis.
  • High-performance liquid chromatography (HPLC) was utilized for the separation and quantification of the product, demonstrating a strong linear relationship with trichlorfon concentrations and achieving a low detection limit.
  • A new extraction method using sodium dodecyl sulfate (SDS) and solid-phase extraction was developed, improving recovery rates and aligning with the principles of Green Analytical Chemistry by reducing toxic solvent use.

Article Abstract

Trichlorfon has the capacity to catalyze the oxidation of benzidine (4,4'-diamino-biphenyl) to 4-amino-4'-nitro biphenyl in the presence of sodium perborate. The product of the catalyzed reaction was validated by LC-MS method. Reversed-phase high performance liquid chromatography with 365 nm UV detection was used for separation and quantification of 4-amino-4'-nitro biphenyl. It can be proven there is a linear relationship between the peak areas of 4-amino-4'-nitro biphenyl and trichlorfon in the concentration range of 0.02-0.5 mg L(-1) (r=0.9988). Limit of detection was 2.0 microg L(-1). A method for the indirect determination of trichlorfon using HPLC was developed based on catalytic effect of trichlorfon. Method validation was performed on samples spiked at three levels (0.5, 1.0, 1.5 mg kg(-1)), the recoveries ranged from 67.5 to 82.1%, with relative standard deviations between 4.5 and 7.3%. 0.01 mol L(-1) sodium dodecyl sulphate (SDS) solution was used to extract trichlorfon from samples and solid-phase extraction was used to isolate and concentrate trichlorfon in SDS solution. The recoveries of trichlorfon obtained with percolating the extraction through a SPE system were essentially in agreement with those obtained by liquid-liquid extraction. This new isolation technique decreases the use of toxic solvents and satisfies the requirements of Green Analytical Chemistry.

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Source
http://dx.doi.org/10.1016/j.aca.2006.10.045DOI Listing

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