Octanol–air partition coefficients of polybrominated biphenyls

The octanol–air partition coefficients (K_OA) for PBB15, PBB26, PBB31, PBB49, PBB103 and PBB153 were determined as a function of temperature using a gas chromatographic retention time technique with 1,1,1-trichloro-2,2-bis (4-chlorophenyl) ethane (p,p′-DDT) as a reference substance. The internal energies of phase change from octanol to air (Δ_OAU) were calculated for the six compounds and were in the range from 74 to 116 kJ mol⁻¹. Simple regression equations of log K_OA versus relative retention times (RRTs) on gas chromatography (GC), and log K_OA versus molecular connectivity indexes (MCI) were obtained, for which the correlation coefficients (r²) were greater than 0.985 at 283.15 K and 298.15 K. Thus the K_OA values of the remaining PBBs can be predicted by using their RRTs and MCI according to these relationships.     

固相萃取气相色谱法测定地表水中有机磷农药

建立了固相萃取(SPE)气相色谱火焰光度(GC-FPD)检测方法,并且检测了地表水中8种有机磷农药,检测限在0.09～0.26μg/L之间,相对标准偏差为3.1%～9.7%(n=8),加标回收率达到61.3%～103.2%,与传统的气相色谱法相比,该方法具有比较高的重现性和选择性,在地表水有机磷农药的测定中具有很好的应用前景.     

Monitoring the formation of trihalomethanes in the effluents from a shrimp hatchery

Formation of trihalomethanes (THM) was monitored at the Laboratório de Camarões Marinhos (LCM) from the Universidade Federal de Santa Catarina. THM could be present because chlorinated effluents from disinfection are discharged from the different hatchery rooms. THM quantification was done through an analytical methodology using Purge&;Trap coupled with a gas chromatograph equipped with an electron capture detector. Relative standard deviation (RSD), limit of detection (LOD) and limit of quantification (LOQ) for the methodology corresponded to the ranges of 8–17%; 0.01–0.03 μg L^?1 and 0.03–0.08 μg L^?1, respectively. Linear working range was of 0.1–8.0 μg L^?1 for all compounds. Enrichment and recovery method was applied to evaluate possible matrix effects and the results varied from 71.2% to 107.9%. LCM was monitored between August and December, 2004. This study showed that THM did not increase with the increase in postlarvae production and also that the aquatic life and the surrounding environment were not affected.     

土壤中有机氯农药的多残留分析技术

本文建立了超声波提取 ,硅胶SPE柱净化 ,GC μECD检测土壤中α HCH ,β HCH ,γ HCH ,δ HCH ,HCB ,o p′ DDE ,aES,p p′ DDE ,Diel,Endrin ,p p′ DDD ,o p′ DDT ,p p′ DDT含量的方法 .对提取剂、洗脱剂和前处理步骤优化的结果表明 :体积比为 1∶2的丙酮 /石油醚是较好的提取剂和洗脱剂 ,方法加标回收率在 70 %— 1 1 0 %之间 ,检测限为0 0 5— 1ng·g- 1 .     

大气中苯乙烯的气相色谱法测定

采用活性炭管吸附大气中基苯乙烯，以二硫化碳洗脱，以溴水加成后，用气相色谱电子捕获器测定苯乙烯的二溴加成物。本方法适合于检测多种污染物共存的大气中痕量苯乙烯。其线性范围为０．０１５－０．７４ｎｇ，最低检出浓度为０．００１ｍｇ／ｍ＾３；重现性实验的变异系数为２．３％：当活性炭管吸附苯乙烯在２．９μｇ时，回收率为９０％，吸附苯乙烯０．２９μｇ时，回收率为７２％。     

顶空-气相色谱法测定水质中的丙酮和丁酮

本文建立顶空-气相色谱法测定水和废水中的丙酮和丁酮的方法,水样测定结果的相对偏差小于5.0%,加标回收率在91%～103%之间,最低检出浓度0.006 mg.L-1。该方法简便,灵敏度更高,重现性好,线性范围宽,精密度和准确度满意,尤其是避免了消耗大量有机试剂,避免二次污染。旨在为实验分析人员提供技术参考依据。     

Biodegradation of α and β Endosulfan in Soil as Influenced by Application of Different Organic Materials

Abstract

A laboratory pot experiment was conducted to study the effect of amending soil with four different sources of organic matter on the degradation rate of α and β endosulfan isomers. Poultry by-product meal, poultry manure, dairy manure, and municipal solid waste compost were cured, dried, ground (<1 mm) and thoroughly mixed with a calcareous soil at a rate of 2% and placed in plastic pots. Endosulfan was added at the rate of 20 mg kg⁻¹. The moisture level was kept near field capacity and the pots were kept at room temperature. Soil sub-samples, 100 g each, were collected from every pot at days 1, 8, 15, 22, 29, 43, and 57 for the measurement of endosulfan isomers. Endosulfan residues were extracted from the soil samples with acetone. The supernatant was filtered through anhydrous sodium sulphate, 5 mL aliquot was diluted to 25 mL with hexane, mixed well, and then two sub-samples from the filtrates were analyzed for α and β endosulfan isomers by gas chromatography. The results indicated that the half-life (T _½) of α-endosulfan in the poultry by-product meal treatment was 15 days compared to about 22 days in the other treatments. The T _½ of β-endosulfan was 22 days in the poultry by-product meal treatment and followed a bi-phasic pattern, 57 days in the municipal solid waste compost treatment and the extrapolated T _½ was about 115 days for the other three treatments.     

气相色谱法测定苯酚生产废水中芳香族化合物

建立了用气相色谱法同时测定苯酚生产废水中异丙苯、α-甲基苯乙烯、α-甲基苯甲醇、2-苯基-2-丙醇、苯酚、苯乙酮、2-苯基丙醛等7种芳香族有毒有机污染物的定量分析方法。采用二氯甲烷对水样进行萃取后进行分析测定,气相色谱条件:DB-WAX型色谱柱,FID检测器,程序升温,进样量1μL。方法的检出限、精密度、回收率实验表明,该方法对苯酚生产废水中各污染物组分具有较好的分离效果,对7种物质的检测限均低于0.05 mg/L,5次测定的相对标准偏差小于5%,实际水样的加标回收率大于97%。     

水中丙烯酰胺气相色谱测定方法研究

研究建立了大口径毛细管柱气相色谱法测定水中丙烯酰胺的方法。优化了水中丙烯酰胺的衍生化条件,用乙酸乙酯和正己烷混合溶剂萃取衍生产物,萃取后直接进行色谱分离分析,水中丙烯酰胺的最低检测浓度为0.05μg/L,回收率在94.5%～113%之间;进行6次平行精密度试验,相对标准偏差低于11.5%。研究建立的气相色谱法简便、快速、准确、重现性好,定量、定性准确可靠,适合水中丙烯酰胺的分析测定。     

固相微萃取-气相色谱法测定水源地水中SVOC

采用固相微萃取-毛细管柱电子捕获气相色谱法测定水源地水中18种半挥发性有机物,优化了萃取纤维、时间、温度、pH值、转子转速、离子强度等萃取条件。方法线性良好,18种化合物的检出限为0.000 2μg/L~0.1μg/L,实际水样加标回收率为84.3%~109%。