农药厂搬迁厂址用于房地产开发的选址环境影响评价

传统有机磷、有机氯农药具有高毒性、持久性和环境激素效应,处于痕量和超痕量浓度水平都可能给人类生命健康和生态环境带来严重威胁和风险。由于农药及其副产物的历史残留、累积及跨界迁移和分布,农药厂搬迁厂址用于房地产开发场地环评具有很大困难。结合南方某市一大型农药厂搬迁厂址用于房地产开发项目的案例,探讨了该类场地评价中基础资料的搜集方法和环评中应遵循的理念和原则。     

岩溶地下河系统中有机氯的分布特征与来源分析

选取重庆老龙洞、青木关岩溶地下河为研究对象,采用气相色谱仪-微池电子捕获检测器(GC-μECD)分析两条地下河水体中21种有机氯农药(OCPs)的浓度.结果表明,南山地下河中六六六(HCHs)和艾氏剂类化合物(ALDs)是主要检出物,青木关地下河中HCHs和甲氧滴滴涕是主要检出物.南山、青木关地下河中均未检出o,p'-DDE、p,p'-DDE、o,p'-DDD,同时,青木关地下河还未检出o,p'-DDT、狄氏剂,其余OCPs在两条地下河中检出率高达100%.青木关地下河中OCPs浓度范围为145~278 ng·L-1之间,平均值为213 ng·L-1;南山老龙洞地下河中OCPs浓度介于17.7~40.8 ng·L-1之间,平均值为32.7ng·L-1.两条地下河中各OCPs组分表现为地下河出口大于入口.通过对OCPs污染来源分析,发现两地下河流域滴滴涕(DDTs)主要来自于历史上工业DDTs输入,氯丹主要来自于大气沉降.六六六(HCHs)主要来源是林丹的输入,南山地下河属于历史污染,青木关地下河上游的甘家槽有新的HCHs输入.与国内外其他各水体相比,南山地下河水体中HCHs、DDTs浓度处于低水平;青木关下河处于中等偏高水平.结合中外用水卫生标准,发现南山地下河和青木关地下河未超过饮水安全标准.青木关应禁止农田施用有机氯农药,保护地下河生态环境.     

大连市化肥农药流失入海量分析

对1996~2000年间,大连市化肥农药使用现状进行了统计分析,运用不同类型有机物理论化学耗氧量的数学计算模型,分别计算了大连市化肥农药流失和工业废水排放对海域的污染影响,结果认为大连市化肥农药流失对海域污染物COD的污染贡献率远远大于工业废水排放的COD贡献率。最终提出应采取加强化肥农药使用管理等有效手段防治近岸海域化肥农药流失污染。     

手性污染物与环境安全

本文就手性污染物在生命过程中对映体的差异作了简要评述,分析了手性污染物对映体的毒性差异及机理.同时指出了手性污染物今后研究的发展趋势.     

检测水中有机磷农药的酶传感器

采用丝网印刷技术制作厚膜型电极,通过交联法将乙酰胆碱酯酶固定在电极上,开发快速检测水中有机磷农药的酶传感器.采用循环伏安法对电极所做的检测结果表明电极彼此间的差异在10%以内,具有较好的一致性.通过在交联剂、酶和底物等方面优化传感器的工作参数,确定了戊二醛、酶和底物的浓度分别为0.2%、0.5 mg/mL和10 mmol/L时,传感器响应最好.在交联固定酶的情况下,根据酶活受到有机磷抑制的原理,采用时间-电流法对特丁硫磷和对硫磷进行了检测.结果表明:这2种有机磷的检测限都可以达到1 ng/mL,线性区间1～10 000ng/mL.在物理吸附固定酶的情况下,采用循环伏安法对特丁硫磷进行了检测.结果表明:采用循环伏安法检测的灵敏度比采用时间-电流法的灵敏度要高.     

气相色谱法测定土壤中37种有机磷农药残留

采用气相色谱法测定土壤中37种有机磷农药,当取样量为10 g时,37种有机磷农药方法检出限为0. 002～0. 015 mg/kg,测定下限为0. 008～0. 060 mg/kg。低含量加标样品中有机磷农药的加标回收率为72. 8%～104%,相对标准偏差为4. 2%～13. 8%;中含量加标样品中有机磷农药的加标回收率为71. 5%～101%,相对标准偏差为4. 3%～13. 5%;高含量加标样品中有机磷农药的加标回收率为74. 6%～109%,相对标准偏差为6. 8%～14. 6%。该方法灵敏度高、分离效果好、重现性好,能够满足土壤中37种有机磷农药残留检测的要求。     

大体积进样-气相色谱法测定水中多种痕量有机磷农药

建立了大体积进样气相色谱-火焰光度法检测水中多种痕量有机磷农药的方法.重点研究了程序升温汽化(PTV)进样条件的选择,通过对分流排空量、吹扫时间、PIV起始温度等PTV参数的选择,优化了测试条件,提高了检测灵敏度.水中9种有机磷农药的线性良好,10ml水样中三乙基偶磷硫酯的检出限为0.01μg/L,硫磷嗪、致螟磷、甲拌磷、乐果、乙拌磷、甲基对硫磷、对硫磷和氨磺磷的检出限可达0.001μg/L.水中添加多种有机磷农药准确度精密度试验,平均回收率为85.8%～108%,相对标准差在3.3%～11.4%之间.与常规方法相比,该方法前处理简单快速、分析成本低.灵敏度、准确度和精密度均符合地表水检测质量的要求,适用于水环境中多种农药残留的快速检测.     

溶剂效应对有机氯农药测定的影响研究

采用气相色谱-质谱法(GC-MS)研究了不同溶剂对有机氯农药测定的影响。结果表明,有机氯农药在不同溶剂中的GC-MS响应值是有差异的,但保留时间不变,且随着有机氯农药质量浓度的增加,这种溶剂效应对大部分有机氯农药的作用减弱。经分析溶剂的极性对有机氯农药测定有显著的影响。     

Bioconcentration and half-life of quinalphos pesticide in rice-fish integration system in the Mekong Delta,Vietnam

In order to determine the distribution and enable the elimination of quinalphos, a popular active pesticide compound used in the Mekong Delta, an experiment was set up in a rice-fish integration system in Can Tho City, Vietnam. Fish was stocked into the field when the rice was two-months old. Quinalphos was applied twice in doses of 42.5 g per 1000 m². Water, fish and sediment samples were collected at time intervals and analyzed by a Gas Chromatography Electron Capture Detector system. The results show that quinalphos residues in fish muscles were much higher than those of the water and the bioconcentration factor (logBCF) was above 2 for the fish. The half-life of first and second quinalphos applications were 12.2 and 11.1 days for sediment, 2.5 and 1.1 days for silver barb, 1.9 and 1.3 days for common carp, and 1.1 and 1.0 days for water, respectively.     

Arsenic residue in residential area after cleanup of pesticide illegal dumping sources in Thanh Hoa province,Central Vietnam

In Vietnam, Nicotex's site is perhaps the most infamous case of illegal disposal of toxic pesticides near residential areas. In 2013, affected villagers discovered illegal burials of around 1,000 tons of expired pesticides in the Nicotex factory. Organic pesticides were detected in illegal burial areas (IBAs) around 60 times greater than acceptable levels, but no attention was paid to contamination of metals, metalloids, and other classes of organic contaminants, which could be co-contaminants in pesticide formulation. This study assessed the contaminants remaining in the IBAs and surrounding residential areas two years after the source removal conducted in 2014. Additionally, a preliminary health risk assessment from residual contaminants was performed. Nine classes of chemicals including parental pesticides, inorganic and organic degradation byproducts, and metals and metalloids, comprising 123 chemicals were quantified in soil, sediment, and water samples from Nicotex and surrounding residential areas. Although concentrations of organic pesticides were below acceptable levels, arsenic contamination in the soil in a Nicotex IBA named NCT5 and Nap village (NV) exceeded the acceptable level. The enrichment factor and log-probability plot indicate that arsenic enrichment at NV is not from natural sources but is associated with arsenic contamination in NCT5. Arsenic may be a co-contaminant in pesticide manufacturing or an arsenical pesticide, such as monosodium methanearsonate. Arsenic found in NV was toxic arsenate for which the preliminary risk assessment yielded an unacceptable excess carcinogenic risk (1 × 10^?4). While all attention was paid to investigate and treat contamination of organic pesticides, it turns out that arsenic is the major existing threat which poses an unacceptable cancer risk in good agreement with the high cancer rate claimed by villagers near Nicotex. This justifies the need for further investigation of the extent of the arsenic contamination and restoration of the contaminated land.