固相净化气相色谱法测定水产品中多种有机磷农药残留

建立了水产品中8种有机磷农药残留同时测定的方法,选择乙腈提取,ENVI-C18串联PSA固相萃取柱净化,经丙酮/正己烷混合溶液（体积比1∶1）洗脱,洗脱液氮吹浓缩后采用气相色谱外标法定量。8种有机磷农药在0.050 mg/L～1.00 mg/L范围内线性良好,检出限在1.8 μg/kg～2.5 μg/kg之间,3个添加水平加标样品平行测定的相对标准偏差为1.1%～5.7%,回收率为69.8%～116%。     

中空纤维膜萃取-气相色谱法测定水中有机氯农药

提出了中空纤维膜萃取-气相色谱法测定水中有机氯农药的方法。首先研究了8种有机氯农药的线性范围,然后测定了中空纤维膜萃取对水中有机氯农药的回收率,最后用中空纤维膜萃取-气相色谱法对实际水样进行检测。结果表明,8种有机氯农药在0.5~10μg/L范围内具有良好的线性关系,中空纤维膜萃取法对水中8种有机氯农药的富集倍数为389~464,回收率为77%~92%,可以满足分析要求。     

固相萃取-气相色谱法测定水环境中邻苯二甲酸酯

采用固相萃取法对水样进行提取富集,气相色谱法测定水中6种邻苯二甲酸酯类有机污染物,并对方法进行了探索、优化和验证。对水体pH在固相萃取过程中对邻苯二甲酸酯萃取回收率的影响进行了研究,解决了邻苯二甲酸2-乙基己基酯和邻苯二甲酸二正辛酯回收率不高的问题。在空白水加标实验中,邻苯二甲酸酯的回收率能达到93.2%~116.3%。除此之外,还对工业废水和地表水进行了加标回收实验,获得了较高的回收率及测定精度。     

分散液液微萃取与超高效液相色谱-串联质谱联用测定土壤和沉积物中三丁基锡

建立了分散液液微萃取与超高效液相色谱-串联质谱联用技术测定土壤和沉积物中三丁基锡的方法。考察了影响分散液液微萃取的因素(包括有机萃取溶剂、萃取剂体积、分散剂、分散剂体积、萃取时间和盐效应)。在最佳实验条件下,方法在0.5~50μg/kg范围内线性关系良好,相关性系数为0.999 0,方法检出限(3倍信噪比)为0.1μg/kg,加标回收率为83.1%~104%,相对标准偏差小于8.5%(n=6),适用于土壤和沉积物中三丁基锡的检测。     

固相萃取-液相色谱-串联质谱法测定水中5种雌激素

建立了固相萃取-液相色谱-串联质谱组合联用技术同时测定地表水、饮用水和污水处理厂出厂水中的5种雌激素(17β-雌二醇、雌三醇、雌酮、17α-炔雌醇、己烯雌酚)的方法。水样经过全自动固相萃取仪富集,以OASIS HLB柱为萃取柱,甲醇为洗脱剂,用液相色谱-串联四极杆质谱联用仪分析定量。分别在0.5~8、5~80μg/L范围内线性良好,相关系数为0.995~0.998。17β-雌二醇、雌三醇、17α-炔雌醇的检出限均为5μg/L,雌酮与己烯雌酚的检出限为0.5μg/L。5种雌激素的纯水加标回收率为63.6%~120.2%,地表水加标回收率为59.8%~91.5%,自来水加标回收率为55.3%~92.1%,精密度为3.7%~10.7%,该方法简单、可靠,可用于水中雌激素类污染物的同时测定。     

液液萃取-气相色谱法测定饮用水中硝基苯类化合物

采用液液萃取－气相色谱法测定饮用水中10种硝基苯类化合物,通过萃取条件优化试验,选择正己烷为萃取剂,使目标物在0μg／L～38.5μg／L之间线性良好,检出限为0.002μg／L ～0．005μg／L。实际饮用水样的加标回收率为80.8％～104％,RSD＜3％。用该方法测定桂林市4个水厂饮用水,结果硝基苯、间－二硝基苯、2,4－二硝基氯苯未检出,其余7种硝基苯类化合物虽有检出,但检出值均低于标准规定的限值。     

GC-MS检测济南市东部空气中气相与颗粒物上有机污染物

用GDX-101吸附剂和玻璃纤维滤膜(GF)同时采集气相和颗粒物上有机污染物,样品经提取分离后用GC-MS进行定性分析.结果表明,颗粒物上有机污染物的种类和含量都高于气相,工业区空气中有机污染较生活区严重,仍以燃煤、燃油污染为主.     

新型侧链聚硅氧烷液晶高分子用作毛细柱气相色谱固定液的研究

以合成的新型胆甾酯类侧链聚硅氧烷液晶高分子作固定液 ,涂渍在弹性石英毛细管柱上 ,具有较高的柱效和选择性 ,热稳定性好 ,适于分离多种异构体混合物。     

Dense Nonaqueous Phase Liquid Tracer Tests: Experimental Results

Two dense nonaqueous phase liquid (DNAPL) tracer tests werecarried out in a shallow aquifer north of Fort Worth, TX. i-Propanolwas used as the nonpartitioning tracer; n-hexanol and n-octanol werethe partitioning tracers. Field data, mathematical modeling, theresults of column tests, and field tracer tests with NaCl were usedin designing the DNAPL tracer tests. The results indicated the presenceof DNAPL at both sites tested; semi-quantitative estimates of theamounts of DNAPL present were obtained by mathematical modeling.Interpretation was complicated by heterogeneity of the aquifer andmass transport effects.     

Enrichment and fractionation of heavy metals in bed sediments of River Narmada, India

A metal fractionation study on bed sediments of River Narmada in Central India has been carried out to examine the enrichment and partitioning of different metal species between five geochemical phases (exchangeable fraction, carbonate fraction, Fe/Mn oxide fraction, organic fraction and residual fraction). The river receives toxic substances through a large number of tributaries and drains flowing in the catchment of the river. The toxic substances of particular interest are heavy metals derived from urban runoff as well as municipal sewage and industrial effluents. Heavy metals entering the river get adsorbed onto the suspended sediments, which in due course of time settle down in the bottom of the river. In this study fractionation of metal ions has been carried out with the objective to determine the eco-toxic potential of metal ions. Although, in most cases (except iron) the average trace/heavy metal concentrations in sediments were higher than the standard shale values, the risk assessment code as applied to the present study reveals that only about 1–3% of manganese, <1% of copper, 16–19% of nickel, 4–20% of chromium, 1–4% of lead, 8–13% of cadmium and 1–3% of zinc exist in exchangeable fraction and therefore falls under low to medium risk category. According to the Geo-accumulation Index (GAI), cadmium shows high accumulation in the river sediments, rest of other metals are under unpolluted to moderately polluted class.