Determination of Haloacetic Acids in Water by LC/MS
Zhanpin Wu, Robert B. Cody, Jeol Usa
Abstract
Zhanpin Wu, Robert B. Cody, Jeol Usa
Abstract
Introduction oacetic acids (HAAs) are disinfection byproducts (DBPs) of the chlorination of drinking water. Dichloroacetic acid and trichloroacetic acid are animal carcinogens. We present an ion-pair HPLC and negative electrospray ionization mass spectrometry (ESI-MS) method with a “function-switching” feature for analysis of all 9 haloacetic acids, monochloroacetic acid (MCAA), dichloroacetic acid (DCAA), monobromoacetic acid (MBAA), bromochloroacetic acid (BCAA), dibromoacetic acid (DBAA), bromodichloroacetic acid (BDCAA), trichloroacetic acid (TCAA), chlorodibromoacetic acid (CDBAA), and tribromoacetic acid (TBAA). JEOL MassCenter™ software can switch different MS settings by the time course. This “function-switching” feature enables each HAA to be analyzed under its optimized MS conditions so that the highest sensitivity can be achieved. Using triethylamine (TEA) as an ion-pairing reagent, a good HPLC separation of all 9 HAAs has been achieved. The optimized MS conditions for each HAA were evaluated.
OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Introduction oacetic acids (HAAs) are disinfection byproducts (DBPs) of the chlorination of drinking water. Dichloroacetic acid and trichloroacetic acid are animal carcinogens. We present an ion-pair HPLC and negative electrospray ionization mass spectrometry (ESI-MS) method with a “function-switching” feature for analysis of all 9 haloacetic acids, monochloroacetic acid (MCAA), dichloroacetic acid (DCAA), monobromoacetic acid (MBAA), bromochloroacetic acid (BCAA), dibromoacetic acid (DBAA), bromodichloroacetic acid (BDCAA), trichloroacetic acid (TCAA), chlorodibromoacetic acid (CDBAA), and tribromoacetic acid (TBAA). JEOL MassCenter™ software can switch different MS settings by the time course. This “function-switching” feature enables each HAA to be analyzed under its optimized MS conditions so that the highest sensitivity can be achieved. Using triethylamine (TEA) as an ion-pairing reagent, a good HPLC separation of all 9 HAAs has been achieved. The optimized MS conditions for each HAA were evaluated.
Key concepts: Dichloroacetic acid, Haloacetic acids, Chemistry, Trichloroacetic acid, Chromatography, Electrospray ionization, Reagent, Mass spectrometry