Combination of microporous membrane liquid-liquid extraction and capillary electrophoresis for the analysis of aromatic amines in water samples [An article from: Analytica Chimica Acta]
Book Details
Author(s)Q. Zhou, G. Jiang, J. Liu, Y. Cai
PublisherElsevier
ISBN / ASINB000RR01L4
ISBN-13978B000RR01L1
AvailabilityAvailable for download now
MarketplaceUnited States 🇺🇸
Description
This digital document is a journal article from Analytica Chimica Acta, published by Elsevier in 2004. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
A method has been established for the simultaneous analysis of eight aromatic amines in water samples by the combination of capillary zone electrophoresis and microporous membrane liquid-liquid extraction (MMLLE). Eight aromatic amines including N,N-dimethylaniline, m-methylaniline, 3,4-dimethylaniline, 2-naphthylamine, 1-naphthylamine, 4-aminobiphenyl, 2-chloroaniline and 2,4-chloroaniline were well separated under optimal separation conditions. The influence factors relevant to the MMLLE process were investigated and the final optimized parameters were used for analysis. The correlation coefficients were excellent with R^2 values larger than 0.99 and the detection limits (S/N=3) were in the range of 0.16-7.5ngml^-^1. The precision and recoveries were within the ranges of 1.7-13.5 and 78.8-112.6%, respectively.
Description:
A method has been established for the simultaneous analysis of eight aromatic amines in water samples by the combination of capillary zone electrophoresis and microporous membrane liquid-liquid extraction (MMLLE). Eight aromatic amines including N,N-dimethylaniline, m-methylaniline, 3,4-dimethylaniline, 2-naphthylamine, 1-naphthylamine, 4-aminobiphenyl, 2-chloroaniline and 2,4-chloroaniline were well separated under optimal separation conditions. The influence factors relevant to the MMLLE process were investigated and the final optimized parameters were used for analysis. The correlation coefficients were excellent with R^2 values larger than 0.99 and the detection limits (S/N=3) were in the range of 0.16-7.5ngml^-^1. The precision and recoveries were within the ranges of 1.7-13.5 and 78.8-112.6%, respectively.
