饮用水中九种卤乙酰胺的高效液相色谱-三重四极杆质谱测定方法
Determination of nine haloacetamides in drinking water using high performance liquid chromatography-triple quadropole mass spectrometry
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摘要: 本文应用固相萃取前处理方法和高效液相色谱-三重四极杆电喷雾质谱(HPLC-ESI/tqMS),优化并建立了9种氯代和溴代乙酰胺的同时测定方法.结果显示,在流动相甲醇/水(5/95,V/V)、流速0.3 mL·min-1、正离子模式条件下,9种卤乙酰胺的线性范围是5-200 μg·L-1或10-500 μg·L-1(R2>0.99),9种卤乙酰胺检出限为0.5-9.2 μg·L-1.经过比较HLB是最优的固相萃取柱.在0.02、0.2、0.5 μg·L-1的3个加标水平下,9种卤乙酰胺的回收率分别为61%-84%、60%-93%和70%-104%,相对标准偏差为1.7%-4.4%、1.1%-4.1%和0.8%-4.1%.
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关键词:
- 高效液相色谱-三重四极杆质谱 /
- 卤乙酰胺 /
- 消毒副产物 /
- 前处理 /
- 饮用水
Abstract: In this study, a new method for the simultaneous determination of nine chlorinated and brominated haloacetamides in drinking water was developed using solid phase extraction (SPE) and high performance liquid chromatography-triple quadropole mass spectrometry (HPLC-tqMS) with positive electron spray ionization. The optimized HPLC mobile phase was composed of methanol and water (5/95, V/V) with a flow rate of 0.3 mL·min-1. The linear ranges of the HPLC-tqMS method were 5-200 μg·L-1 or 10-500 μg·L-1 (R2>0.99) for the nine haloacetamides. The detection limits of the nine haloacetamides were 0.5-9.2 μg·L-1. HLB column was found to be the optimal SPE column. With the spiked concentrations of 0.02, 0.2 and 0.5 μg·L-1, the recovery rates of the nine haloacetamides were 61%-84%, 60%-93% and 70%-104%, respectively (relative standard deviations were 1.7%-4.4%, 1.1%-4.1% and 0.8%-4.1%, respectively). -
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