首页|离子色谱法测定饮用水中高氯酸盐方法研究

离子色谱法测定饮用水中高氯酸盐方法研究

扫码查看
建立了采用离子色谱仪检测饮用水样中微量高氯酸盐的分析方法.样品采集后经 0.22μm微孔滤膜过滤除杂后直接上机检测,进样量为 100 μL.使用Ion PacAS19 分析柱作为色谱柱,柱温 30℃,电导池温度为 35℃.以45.0 mmol/L氢氧化钾溶液作为淋洗液进行在线梯度淋洗,淋洗液流量为 1.0 mL/min.研究结果表明,高氯酸盐质量浓度在0~0.500 mg/L范围内线性关系良好,相关系数R2=0.999 9,加标回收率为 96.0%~98.5%,检出限(S/N=3)为0.005 mg/L,定量限(S/N=10)为0.015 mg/L,相对标准偏差RSD为0.46%.该方法保留时间较短,加标回收率较高,检出限较低,可满足我国的生活饮用水卫生标准中高氯酸盐限量质量浓度(0.07 mg/L)检出要求,适用于大批量生活饮用水中高氯酸的检测.
Study on the Determination of Perchlorate in Drinking Water by Ion Chromatography
An analytical for deterniination of trace amounts of perchlorate in drinking water was established by ion chromatography.After the sample was collected,it was filtered by 0.22 μm microporous filter membrane to remove insoluble matter and then introduced into ion chromatography with sample injection of 100 μL.Use Ion PacAS19 analytical column as the chromatographic column,with a column temperature of 30℃and a conductivity cell temperature of 35℃.Use 45.0 mmol/L potassium hydroxide solution as the eluent for online gradient elution,with a flow rate of 1.0 mL/min.The results indicated that perchlorate had good linearity within the range of 0~0.500 mg/L.The correlation ooefficient was 0.9999 and the adding standard recoveries were 96.0%~98.5%.The method detection limit(S/N=3)was 0.005 mg/L,determination limit(S/N=10)was 0.015 mg/L,and the relative standard deviations RSD was 0.46%.This method has a shorter retention time,higher recovery rate of the added standard,and lower detection limit,which can meet meet the detection requirements of the perchlorate limit mass concentration(0.07 mg/L)of drinking water quality standards in our country and suitable for the detection of perchlorate in a large number of drinking water samples.

drinking waterion chromatographyperchlorate

张燕娣、蒋才斌

展开 >

广西壮族自治区产品质量检验研究院,广西 南宁 530020

饮用水 离子色谱法 高氯酸盐

2024

山西化工
山西省煤化工发展促进中心 山西省化工学会

山西化工

影响因子:0.293
ISSN:1004-7050
年,卷(期):2024.44(11)