A 50-year record of dichloro-diphenyl-trichloroethanes and hexachloro-cyclohexanes in lake sediments and penguin droppings on King George Island, Maritime Antarctic

Since the ban on the use of organochlorine pesticides （OCPs） such as dichloro-diphenyl-trichloroethane （DDT） and hexachlorocyclohexane（HCH） in agriculture, their levels have generally dropped. In a number of cases, however, the levels of these OCPs were found to be unchanging or even increasing after the ban. With the aim to unveil the possible causes of these exceptions, we collected two lake cores from King George Island, West Antarctica, and determined their accumulation flux profiles and temporal trends of these OCPs. In the lake core sediments with glacier meltwater input, the accumulation flux of DDT shows an abnormal peak around 1980s in addition to the expected one in 1960s. In the lake core sediments without glacier meltwater input, the accumulation flux of DDT shows a gradual decline trend after the peak in 1960s. This striking difference in the DDT flux profiles between the two lake cores is most likely caused by the regional climate warming and the resulted discharge of the DDT stored in the Antarctic ice cap into the lakes in the Antarctic glacier frontier. Furthermore, to investigate the change of OCPs loadings in the Antarctic coastal ecosystem, we reconstructed the HCH and DDT concentration profiles in penguin droppings and observed a gradual increase for the former and a continuous decrease for the latter during the past 50 years. The increase of HCH seems to be due to the regional warming from the early 1970s and the resulted HCH discharge to the coastal ecosystem by glaciers＇ meltwater and the illegal use of HCH in the Southern Hemisphere in the recent decade. The different temporal trends of HCH and DDT accumulation rate in the lake core with glacier meltwater input and the aged penguin droppings can be explained by their different water-soluble property.     

气相色谱法测定黄河底泥中多氯联苯及有机氯农药

对黄河底泥样品中多氯联苯及有机氯农药，经索氏提取法处理后，用气相色谱法进行了测定，结果表明：（1）本方法的最低检出限为0.05-0.5ug/kg，达到了微量分析的要求。（2）采集的黄河底泥样品中，多氯联苯及有机氯农药污染较轻。（3）加标回收实验中，多氯联苯的回收率为68．8％－107％,有机氯农药的回收率为40．8％－81．1％。     

环境激素类有机氯农药的用途和危害

介绍了世界自然基金会<环境中被报告具有生殖和内分泌干扰作用的化学物质清单>中16种环境激素类有机氯农药的污染状况、基本概况、用途、危害以及针对有机氯农药污染的治理措施.     

珠江水系两条重要河流水体中悬浮颗粒物的有机污染物含量

为确定珠江三角洲水体悬浮颗粒物中多环芳烃和有机氯农药的含量和来源,对珠江上游的两条重要支流西江、北江水体中的悬浮颗粒物分期进行了两次采样分析,测定了水体中悬浮颗粒物的含量,分析了其中多环芳烃、有机氯农药的含量。其中,北江水体中悬浮颗粒物中的PAHs的总量分别为928.8、1259.7ng·g-1干质量,西江水体中悬浮颗粒物的PAHs总量分别为660.1、1130.7ng·g-1干质量,其来源主要为石化燃料的燃烧与排放。北江水体悬浮颗粒物中的有机氯农药总量为41.9、135.3ng·g-1干质量,西江为78.54、108.7ng·g-1干质量,由沿岸农田排放入水体。并发现,西江北江沿岸的农田,仍旧在使用DDT、硫丹等农药。     

天氧附着膜膨胀床反应器预处理有机氯农药废水的研究

针对有机氯农药废水可生化性差的特点，研究了采用厌氧膨胀床颗粒活性炭反应器对其预处理以提高可生化性的效果。未经处理的有机氯农药废水及经混凝、Fenton氧化处理后的有机氯农药废水分别进入厌氧反应器，在进水pH为6．8～7．2，水力停留时间为48h，有机物容积负荷为1．41～3．19kgCOD／m^2．d时，3种废水的出水B／C值分别为0．35、0．41和0．42；出水COD分别为1280、1050和659mg／L；出水色度分别为50倍（灰白）、20倍（灰白）和20倍（灰白）。从运行稳定、经济的角度，选择混凝一厌氧组合作为该农药废水的预处理工艺。研究提出采用单位表面面积生物膜底物降解速率LW作为厌氧膨胀床反应器的设计指标，并根据试验数据得出厌氧膨胀床颗粒活性炭反应器的动力学模型，为工程设计及运行管理提供依据。     

氯代芳香化合物的微生物降解研究

生物技术对消除有毒化学品已显示出广阔的应用前景，深入研究有毒化学品微生物降解的生物化学和遗传学，可按照预期目的构建具有更大降解能力的遗传工程菌株，以促使污染物的无害化资源化。本文对纯菌株降解氯代芳香化合物的降解途径、降解性质粒和遗传工程菌株的构建等诸方面进行了综述。     

天津市郊农田土壤中有机氯农药残留的局地分异

在天津3处典型污灌与非污灌农田各采集了10个表土样品，测定了其中α-HCH，β-HCH，γ-HCH，δ－HCH、p,p'-DDE,p,p'-DDD,p,p'-DDT和p'-DDT等8种有机氯农药含量，籍以研究该地区有机氯农药在地块中的局部分异。结果表明，所研究地块中两类化合物含量均表现出显著的非均一特征。其中污灌土地中的（DDT）以及污灌农田中的HCH含量都具有与灌溉方向密切相关的空间分布特征。这样的规律性空间变异导致他们的空间波动幅度高于其他地块。鉴于上述趋势性和非趋势性空间分异，在开展相关时人有必要在目标地块中采集重复样或混合样。     

苯甲（乙）腈类化合物理化参数的统计和筛选

本文对20个芳香腈化合物的理化参数作了统计分析,得到了乙腈基中—CH_2—基因的电子效应常数为0.2,建立了水解速率常数k与取代基电子效应常数σ的回归方程,pk=5.89,9—2.144σ(R=-0.957,n=20),根据各化合物的因子得分和实验设计方法为生物试验挑选出了5个有代表性的化合物。     

Photocatalytic remediation of γ-HCH contaminated soil induced by α-Fe2O3 and TiO2

Heterogeneous photocatalytic degradation of γ-HCH on soil surfaces was carded out to evaluate the photocatalytic effectiveness of α-Fe2O3 and TiO2 toward degrading γ-HCH on soil surfaces. After being spiked with γ-HCH, soil samples were loaded with α-Fe2O3 or TiO2 and exposed to UV-light irradiation. Different catalyst loads, 0%, 2%, 5%, 7%, and 10% (wt.)α-Fe2O3 ; 0%, 0.5%, 1%, 2:(Wt.)TiO2, were tested for up to 7 d irradiation. The effects of soil thickness, acidity, and humic substances were also investigated. The obtained results indicated that the γ-HCH photodegradation follows the pseudo-first-order kinetics. The addition of α-Fe2O3 or TiO2 accelerates the photodegradation of γ-HCH, while the photodegradation rate decreases when the content of α-Fe2O3 exceeds 7% (wt.).The degradation rate increases with the soil pH value. Humic substances inhibit the photocatalytic degradation of γ-HCH., and trichlorobenzene are detected as photodegradation intermediates, which are gradually degraded with the photodegradation evolution.     

混床填色谱柱在有机氯农药残留分析中的应用

在植物粮食、土壤有机氯农药残留监测，使用涂有ＯＶ－１７和ＱＦ－１固定液的白色载体ＣｈｒｏｍｏｓｏｒｂＷ，该种色谱柱对六六六的四种异构体分离比较好，但对ＤＤＴ的四种异构体分离不理想，采用红色载体ＣｈｒｏｍｏｓｏｒｂＰ和白色载体ＣｈｏｍｏｓｏｒｂＷ湿床填充的色谱柱，分离有机氯农药８种组份仅需１５分钟，提高了有机氯农药的分离分析效果。