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作 者:王莎莎 李霈 冉金凤 董南[1] WANG Sha-sha;LI Pei;RANJin-feng;DONG Nan(School of Chemistry and Chemical Engineering,Guizhou University,Guiyang550025,China)
机构地区:[1]贵州大学化学与化工学院,贵州贵阳550025
出 处:《广州化学》2021年第4期57-64,共8页Guangzhou Chemistry
基 金:国家自然科学基金项目(21665005)资助。
摘 要:以单羟基七元瓜环(Q[7]-OH)和端羟基聚二甲基硅氧烷(OH-PDMS)为固定相,利用溶胶-凝胶方法制备了PDMS/Q[7]-OH的固相微萃取纤维(SPME fiber)。建立了PDMS/Q[7]-OH SPME纤维-气相色谱(GC)/氢火焰离子化检测器(FID)对环境水样中5种苯酚类化合物同时检测的分析方法。实验结果表明5种酚类化合物的线性范围在0.5~5000μg/L之间,相关系数均大于0.9940。方法的检出限(LOD)在0.1~3.1μg/L范围内,富集倍数为6~104倍。三个加标浓度的平均相对回收率(n=3)在70.1%~113.7%范围内,日内及日间精密度的RSD在3.2%~9.9%之间(n=5,c=500μg/L)。方法灵敏、简便,可满足环境水样中苯酚类化合物同时测定的要求。Solid phase microextraction fiber(SPME fiber)based on PDMS/Q[7]-OH was prepared by sol-gel method using hydroxyl-terminated polydimethylsiloxane(OH-PDMS)and monohydroxy-cucurbit[7]uril(Q[7]-OH)as stationary.A PDMS/Q[7]-OH SPME fiber-gas chromatography with flame ionization detector(GC/FID)method was developed for the simultaneous determination of five phenols in environmental water samples.The results indicated that the linear range was 0.5~5000μg/L with correlation coefficient(R)>0.9940.The limits of detection of the proposed method were in the range of 0.1~3.1μg/L and an enrichment factor were between 6 and 104 fold.The mean relative recoveries(n=3)at three spiked levels ranged from 70.1%to 113.7%,with intra-precision and inter-precision both in the range of 3.2%~9.9%.The proposed method was simple and sensitive,and was suitable for the simultaneous analysis of phenols in environmental water.
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