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作 者:者为[1] 范多青[1] 王庆华[1] 李响丽[1] 王文元[1] 史小波[1]
机构地区:[1]红云红河烟草集团有限责任公司技术中心,云南昆明650202
出 处:《分析测试学报》2012年第6期734-737,共4页Journal of Instrumental Analysis
基 金:国家烟草专卖局标准项目资助
摘 要:建立了一种离子色谱电导检测法测定水基胶黏剂中氨残留的方法。样品经10 mmol/L盐酸水溶液振荡、离心、过滤提取后,采用阳离子交换色谱柱分离和电导检测。在优化实验条件下,样品中的氨在0.05~2.0 mg/L范围内呈良好的线性关系(r2=0.999 8),加标回收率在93%~102%之间,相对标准偏差不高于4.3%,检出限(S/N=3)为0.007 mg/L,定量下限(S/N=10)为0.024 mg/L。结果表明该方法能够达到定量检测的目的。将该方法用于实际样品检测,结果可靠。通过对氨的稳定性实验发现,处理好的样品宜在12 h内测定。An ion chromatographic (IC) method was developed for the quantitative analysis of ammonia in water-borne adhesives. After extracted with 10 mmol/L hydrochloric acid and purified by oscil- lation eentrifugation and filtration, the ammonia was separated by ion chromatography and detected with electrical conductivity detector. The results showed that the ammonia had a good linearity (r2 = 0. 999 8 ) in the range of 0. 05 - 2.0 mg/L. The detection limit( S/N = 3 ) was 0. 007 mg/L and the quantitation limit ( S/N = 10 ) was 0. 024 mg/L. The average recoveries were between 93% and 102% with relative standard deviations not more than 4.3% . The analysis of real samples verified the reliability of this method. The stability test of ammonia results suggested that the processed samples should be measured in 12 h.
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