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作 者:王成云[1] 沈雅蕾[1] 林君峰[1] 谢堂堂[1] 褚乃清[1]
出 处:《上海纺织科技》2013年第7期56-58,共3页Shanghai Textile Science & Technology
摘 要:建立了一个高效液相色谱方法,对邻氨基苯甲醚及其同分异构体进行分离,从而避免了其同分异构体对邻氨基苯甲醚含量测定的干扰,防止出现假阻性结果。该方法的加标回收率为73.65%-83.69%(皮革制品)和74.89%-84.85%(纺织品),精密度实验RSD均小于5%,d S/N=3的条件下,检出限分别为0.3mg/kg(邻氨基苯甲醚)、0.3mg/kg(间氨基苯甲醚)和0.5mg/kg(对氨基苯甲醚)。该方法简便快捷,定量准确,有效地解决了禁用偶氨染料测试中邻氨基苯甲醚的假阳性结果问题。An effective HPLC method was established to separate o-anisidine and its isomers such as m-anisidine and p-anisidine, in order to avoid false positive result in the analysis of o-anisidine which was susceptible to interference of its isomers. The spiked recoverics varied from 73.65% to 83.69% for leather products, from 74.89% to 84.85% for textiles. The relative standard deviation (RSD) of precision experiments was all less than 5%. At the condition of S/N =3, the detection limit was 0.3, 0.3 and 0.5mg/kg for o-anisidine, m-anisidine and p-anisidine, respectively. The proposed method was simple, rapid and accurate, and the problem of false positive result of o-anisidine in the determination of banned azo dyes was effectively solved.
分 类 号:TS197[轻工技术与工程—纺织化学与染整工程] O657.72[轻工技术与工程—纺织科学与工程]
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