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作 者:朱晓兰[1] 洪深求[2] 李盼盼[1] 高芸[1] 刘渊根[2]
机构地区:[1]中国科学技术大学烟草与健康研究中心,安徽合肥230052 [2]安徽省烟草公司,安徽合肥230022
出 处:《分析测试学报》2012年第3期351-354,358,共5页Journal of Instrumental Analysis
基 金:中央高校基本科研业务费专项资金(WK2061020001);安徽省烟草公司项目资助(20100551004)
摘 要:建立了超声溶剂提取和分散液液微萃取(DLLME)相结合的提取、净化前处理技术,采用气相色谱-质谱法分析了烟用添加剂中的黄樟素、侧柏酮、龙蒿脑、胡薄荷酮、甲基丁香酚、香豆素、6-甲基香豆素和7-甲氧基香豆素8种烷基苯类香味有害物。对分散液液微萃取溶剂及其体积、分散剂及其体积、萃取时间等条件进行了优化。在最佳实验条件下,8种有害物的线性范围为0.4~928μg/L(r2≥0.998 9),检出限为0.04~0.24μg/L,定量下限为0.13~0.80μg/L,富集倍数为140~208倍,方法的加标回收率为90%~100%,相对标准偏差为2.4%~6.7%。与行业推荐的测定方法相比,该方法具有灵敏度高、富集效果好、回收率高等优点。A new ultrasonic-assisted extraction followed by dispersive liquid -liquid micro-extraction (DLLME) and GC - MS analysis method was developed for the simultaneous determination of eight alkenylbenzenes and other flavor-related compounds including safrole, coumarin, 6-methylcoumarin, 7-metheoxycomnarin, estragole, methyleugenol, pulegone and thujone in tobacco additives. The different parameters affecting the whole process such as the type and volume of extraction and dis- perser solvents, the salt addition and the extraction time were studied. Under the optimum condi- tions, the enrichment factors(EF) ranged from 140 to 208. The linear relationships of eight alkenyl- benzenes and other flavor-related compounds were obtained in the range of 0.4 -928 μg/L, with cor- relation coefficients ( r^2 ) over O. 998 9. The limits of detection (LOD) and the limits of quantitation (LOQ) were in the ranges of 0.04 -0.24 μg/L and 0. 13 -0. 80 μg/L, respectively. The average recoveries were in the range of 90% - 100% with relative standard deviatigns (RSDs) of 2.4% - 6.7% . The method was successfully applied in the analysis of real tobacco flavor additive samples. Compared with the industry recommended standard method, lower concentrations of detection were a- chieved due to the high enrichment power of DLLME. Therefore, this method shows tremendous po- tential in trace analysis of alkenylbeuzenes and other flavor-related compounds in real samples.
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