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An Optimized Analytical Method for the Simultaneous Detection of Iodoform, Iodoacetic Acid, and Other Trihalomethanes and Haloacetic Acids in Drinking Water

An optimized method is presented using liquid-liquid extraction and derivatization for the extraction of iodoacetic acid (IAA) and other haloacetic acids (HAA(9)) and direct extraction of iodoform (IF) and other trihalomethanes (THM(4)) from drinking water, followed by detection by gas chromatograph...

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Detalles Bibliográficos
Autores principales: Liu, Xiaolin, Wei, Xiao, Zheng, Weiwei, Jiang, Songhui, Templeton, Michael R., He, Gengsheng, Qu, Weidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628783/
https://www.ncbi.nlm.nih.gov/pubmed/23613747
http://dx.doi.org/10.1371/journal.pone.0060858
Descripción
Sumario:An optimized method is presented using liquid-liquid extraction and derivatization for the extraction of iodoacetic acid (IAA) and other haloacetic acids (HAA(9)) and direct extraction of iodoform (IF) and other trihalomethanes (THM(4)) from drinking water, followed by detection by gas chromatography with electron capture detection (GC-ECD). A Doehlert experimental design was performed to determine the optimum conditions for the five most significant factors in the derivatization step: namely, the volume and concentration of acidic methanol (optimized values  = 15%, 1 mL), the volume and concentration of Na(2)SO(4) solution (129 g/L, 8.5 mL), and the volume of saturated NaHCO(3) solution (1 mL). Also, derivatization time and temperature were optimized by a two-variable Doehlert design, resulting in the following optimized parameters: an extraction time of 11 minutes for IF and THM(4) and 14 minutes for IAA and HAA(9); mass of anhydrous Na(2)SO(4) of 4 g for IF and THM(4) and 16 g for IAA and HAA(9); derivatization time of 160 min and temperature at 40°C. Under optimal conditions, the optimized procedure achieves excellent linearity (R(2) ranges 0.9990–0.9998), low detection limits (0.0008–0.2 µg/L), low quantification limits (0.008–0.4 µg/L), and good recovery (86.6%–106.3%). Intra- and inter-day precision were less than 8.9% and 8.8%, respectively. The method was validated by applying it to the analysis of raw, flocculated, settled, and finished waters collected from a water treatment plant in China.