土壤有机质组分中多环芳烃分配特征和生态风险

土壤有机质是影响多环芳烃（PAHs）环境行为的一个重要因素,不同有机质组分结合的PAHs生物有效性和环境风险有所不同.本文对6个野外污染土壤中15种优控PAHs的含量和组成及其在土壤轻组（LF）和重组（HF）中的分配特征进行了研究,并采用苯并[a]芘（BaP）毒性当量浓度（TEQ_BaP）评价了全土、LF和HF中PAHs的生态风险.结果表明,6个土样中15种PAHs总量范围为8.31×10²~2.97×10⁴μg/kg,4环PAHs百分含量最高,范围为35.7%~59.6%.6个土样LF中PAHs总量范围为2.38×10⁴~1.17×10⁵μg/kg,HF中PAHs总量范围为3.75×10²~2.12×10⁴μg/kg.虽然土壤中LF质量百分比只有1.0%~9.8%,但其结合的PAHs量却占土壤中PAHs总量的5.9%~60.6%.LF中15种PAHs总TEQ_BaP值范围为2.99×10²~1.68×10⁴μg/kg,分别是全土和HF的2.7~33.2倍和3.6~69.5倍.在PAHs污染土壤修复和生态风险评估中,应重视LF中PAHs.对LF中PAHs量占土壤中PAHs总量百分比较高的土壤,可以通过分离LF的方法来修复污染土壤.     

石油烃在非均质包气带中的吸附作用及迁移规律

为深入分析强非均质性污染场地中石油烃的运移规律,探究石油烃类污染物在场地中的吸附、迁移及其影响因素,选取潮白河上游为典型研究区,受冲洪积扇条件控制,区域内包气带非均质性强,地下水埋深较大.采集污染场地包气带介质样品,分别装填原状土（0~20 mm）、细颗粒（< 2 mm）和粗颗粒（>4 mm）3种介质迁移柱,通过土柱淋滤试验表征石油烃在典型介质中的迁移特性;通过静态吸附试验和微生物降解试验识别石油烃迁移过程的关键影响因素,揭示多要素作用条件下的石油烃迁移规律.结果表明:原状土、细颗粒和粗颗粒这3种介质迁移柱出水中石油烃浓度均呈先下降、后波动上升、最终趋于稳定的趋势.3种介质对石油烃的吸附过程均呈现快吸附和慢吸附两个阶段,快吸附阶段发生在试验0~15 h内,完成了吸附的70%~80%;慢吸附阶段持续时间较长,吸附总量缓慢增加.固液比、温度和pH等要素对3种介质石油烃吸附性能的影响相对较小.微生物降解是慢吸附阶段石油烃浓度呈波动上升的主要原因,且在整个石油烃垂向迁移过程中,吸附作用对石油烃去除的贡献率为80%,微生物降解的贡献率为20%.研究显示,相对于微生物作用而言,强非均匀介质在石油烃类污染场地的污染物吸附和迁移过程中起关键控制作用.      

海洋中石油烃敏化光氧化反应研究进展

本文总结了激发三重态光敏剂及激发单重态氧分子引发的表层海水中石油烃光氧化反应的研究概况，介绍激发三重态光敏化剂引发的典型化合物的光氧化产物、反应机理，原油光氧化产物和表层海水中溶解石油烃成分及其氧化产物的分析等方面的研究成果。比较两类光氧化反应研究的优缺点，提出今后研究的方向。     

The Fate in the Marine Environment of a Minor Diesel Fuel Spill from an Antarctic Research Station

Monitoring was undertaken of the fate in the marine environment of an accidental spill of diesel fuel (1000 litres) from Faraday Research Station, Galindez Island, Antarctica in March 1992. On the day after the incident concentrations in seawater reached a maximum of 540 µg 1-1 for n-alkanes and 222 µg 1-1 for polycyclic aromatic hydrocarbons (PAH). However, concentrations returned to local background levels within one week. The fuel had an immediate toxic effect on intertidal limpets in the local station area, and 100 animals were found dead the day after the spill. Surviving animals had elevated concentrations of both n-alkanes and PAH for over a month after the spill, reaching a maximum of 9960 µg kg-1 for n-alkanes and 90 µg kg-1 for PAH 30 days after the spill occurred. This was the result of accumulation from a residue of the diesel being flushed by rainwater into the littoral zone. Seven months after the spill concentrations of both n-alkanes and PAH in limpets living close to the station were still an order of magnitude greater than those found in animals at an uncontaminated control site. This is because limpets living in the littoral zone were continually exposed to chronic but low-level hydrocarbon contamination from station activities. The diesel spill itself had a very minor, localised and short-term impact on the Antarctic marine environment.     

Application of semipermeable membrane device for assessing toxicity in drinking water

Semipermeable membrane devices (SPMDs) mimic passive diffusive transport of bioavailable hydrophobic organic compounds through biological membranes and their partitioning between lipids and environmental levels. Our study was developed on a surface water treatment plant based in Turin, Northern Italy. The investigated plant treats Po River surface water and it supplies about 20% of the drinking water required by Turin city (about one million inhabitants). Surface water (input) and drinking water (output) were monitored with SPMDs from October 2001 to January 2004, over a period of 30 days. The contaminant residues, monthly extracted from SPMDs by dialysis in organic solvent, were tested with the Microtox^TM acute toxic test and with the Ames mutagenicity test. Same extracts were also analyzed with gaschromatography—mass spectrometry technique in order to characterise the organic pollutants sampled, especially Polycyclic Aromatic Hydrocarbons (PAHs).

Although the PAHs mean concentration is about one hundred times lower in the output samples, the mean toxic units are similar in drinking and surface water.

Our data indicate that the SPMD is a suitable tool to assess the possible toxicity in drinking water.     

饮用水中卤代产物及前驱物的形成与控制

简述了目前国内对饮用水中卤代烃类化合物的研究现状，根据对饮用水中卤代产物的形成及浓度受水源水中前驱物、饮用水消毒处理方法等因素的影响，阐述了控制饮用水消毒过程中卤代烃的形成途径。     

低碳烃选择性催化还原NOx的研究进展

对报道较多的以低碳烃作为还原荆，选择性催化还原NO的研究进展进行了综述，重点介绍了离子交换分子筛类催化剂、金属与金属氧化物的研究状况，分析了存在问题及今后的研究重点，简要介绍了固体超强酸类催化荆。     

石油烃类降解菌在不同矿化度下的生长规律及去油效果研究

研究了不同盐浓度含油废水中石油烃类降解菌的生长情况以及对原油的去除效果。实验结果表明:在盐浓度低于15%的石油烃废水中,降解菌生长旺盛,且数量大;在盐浓度为15%～25%的石油烃废水中有较多菌量,但数量已明显减少;在盐浓度为30%以上的石油烃废水中几乎无细菌生长。培养时间为13h时,去油率可达到55%;随着培养时间的延长,原油去除率趋于平缓。高盐度石油烃废水中生存的微生物在处理含油废水方面具有很大的应用潜力。     

内酯型槐糖脂修复石油污染土壤的影响因素

采用内酯型槐糖脂(SL50)修复石油污染土壤。通过单因子实验与正交实验,考察了槐糖脂溶液质量浓度、振荡时间、反应体系初始pH、NaCl加入量以及固液比(土壤质量与表面活性剂溶液体积之比)对污染土壤石油烃洗脱率的影响。单因子模型回归分析结果表明,参数变量均符合二次拟合模型,槐糖脂溶液质量浓度、反应体系初始pH以及NaCl加入量的二次模型拟合效果较好。正交实验结果表明,槐糖脂溶液质量浓度和反应体系初始pH是该实验的敏感性因子,最优洗脱条件为槐糖脂溶液质量浓度40 mg/L、反应体系初始pH 9、NaCl加入量6%(w)。     

油气包裹体在成藏年代学研究中的应用实例分析

本文介绍了烃类流体包裹体在油气成藏期次、成藏年代和成藏史研究方面的应用 ,讨论了该方法在成藏年代学研究中存在的一些问题。指出在运用流体包裹体均一温度进行成藏年代分析时 ,一般应采用共生盐水包裹体的均一温度。认为流体包裹体均一温度确定成藏年代的准确性 ,一方面取决于储层埋藏史和热史模型的可靠性 ,另一方面后期构造热事件也是可能的影响因素。后期热事件可能使包裹体最初形成时的均一温度发生再平衡 ,造成所测的均一温度高于成藏时实际的古地温 ,由此确定的成藏年代将比实际的成藏年代偏晚。