衡水市空气主要污染物体积质量的时间分布特征

利用衡水市环境监测站2005—2007年度大气例行检测的数据,对衡水市大气中主要污染物SO^2、NO^2、PM10体积质量值的逐日数据进行统计分析,得出了衡水市空气污染的现状和时间变化规律：（1）污染物体积质量值的月变化曲线呈槽型分布,非取暖期的空气状况明显好于取暖期,取暖期SO^2平均体积质量是非取暖期的2．45倍;（2）污染物体积质量值的日变化曲线基本为两高两低型,其中取暖期污染指数早晨出现极高值的时间比非取暖期明显偏晚;（3）污染物体积质量值的年变化表明了SO^2的体积质量在降低,而NO^2的体积质量却有了小幅增长。     

Role of Alternative Electron Acceptors (AEA) to control methane flux from waterlogged paddy fields: Case studies in the southern part of West Bengal, India

The rice fields, depleted of O₂, contain large amount of moisture and organic substrates to provide an ideal anaerobic environment for methanogenesis and are one of the principal anthropogenic sources of methane. In order to mitigate this emission Alternative Electron Acceptors (AEA) were altered in the soil. The experiments were carried out in four seasons at the site of Balarampur, near Baruipur, South 24 Parganas, West Bengal, namely September–December, 2005 (Cultivar: Sundari), February–May, 2006 (Cultivar: Sundari), September–December, 2006 and February–May, 2007 (Cultivar: Swarna-Pankaj). The seasonal average methane flux (Fe treated), for the cultivar type “Sundari” (season: September–December, 2005), is 4.41 t ha⁻¹, as compared to the value of 6.40 t ha⁻¹ for the untreated soil. Similarly for February–May, 2006, the seasonal average methane flux (Fe treated) is 5.52 t ha⁻¹, whereas the untreated flux is 5.69 t ha⁻¹. In the third and fourth seasons we had two treatments with Ammonium Thiosulphate and Ferric Hydroxide. The seasonal average methane flux (treatment: Ammonium Thiosulphate) is 4.35 t ha⁻¹ and 5.41 t ha⁻¹ respectively, whereas for the ferric hydroxide treated soil it is 4.35 t ha⁻¹ and 6.14 t ha⁻¹ respectively. The properties related to the nutrient quality of the harvested paddy seeds supplement these results.     

微生物降解石油烃污染物的研究进展

对石油烃污染物的生物处理技术进行了较全面的介绍,总结了国内外在该领域的研究成果.重点介绍了石油烃降解微生物种类、石油烃降解酶、环境影响因素以及微生物降解石油烃技术的应用等方面的研究进展.分析了现有研究中存在的不足,并对今后的研究趋势作了预测和展望.     

Historical change of mercury pollution in remote Yongle archipelago, South China Sea

We collected three ornithogenic coral sand sedimentary profiles from Jinyin Island, Jinqing Island and Guangjin Island of Yongle archipelago, South China Sea and reconstructed the deposition flux of anthropogenic Hg over the past 700 years in the study area. On the whole, the anthropogenic Hg flux is relatively low; it remained at a low level before the Industrial Revolution with a small peak at about 1450-1550 AD, which may record the enhanced metallurgy activity in Ming Dynasty of China. During the 20th century, the deposition flux of anthropogenic Hg increased rapidly, but two troughs occurred during the periods around 1940s and 1970s, corresponding to the economic depression caused by World War II, Civil War in China (1945-1949), and the Culture Revolution (1966-1976) in China. Since the 1970s the deposition flux of anthropogenic Hg has been persistently increasing, apparently the result of fast economic development in East and Southeast Asia countries around South China Sea.     

Formation of PCDD/Fs from oxidation of 2-monochlorophenol over an Fe2O3/silica surface

The role of iron in surface-mediated formation of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) from 2-chlorophenol (2-MCP) was investigated over the temperature range of 200-550 °C under oxidative conditions. In order to compare and contrast with previous work on copper and ferric oxide-mediated pyrolysis of 2-MCP, identical reaction conditions were maintained (50 ppm 2-MCP, model fly-ash particles containing 5% Fe₂O₃ on silica). Observed products included dibenzo-p-dioxin (DD), 1-monochlorodibenzo-p-dioxin (1-MCDD), dibenzofuran (DF), 4,6-dichlorodibenzofuran (4,6-DCDF), 2,4- and 2,6-dichlorophenol, 2,4,6-trichlorophenol, quinone, catechol, chloro-o-quinone, chlorocatechol and polychlorinated benzenes. Yields of DD and 1-MCDD were 2 and 5 times higher than under pyolysis conditions, respectively. Although 4,6-DCDF was the major PCDD/F product formed with a yield that was 2.5× greater than under pyrolysis, the yield of non-chlorinated DF, which was the dominant PCDD/F product under pyrolysis, decreased by a factor of 3. Furthermore, the ∼2× higher yield of PCDDs under oxidative conditions resulted in a PCDD to PCDF ratio of 0.75 compared to a relatively low ratio of 0.39 previously observed under pyrolytic conditions.     

The structure of the fire fighting foam surfactant Forafac®1157 and its biological and photolytic transformation products

For several decades, perfluorooctane sulfonate (PFOS) has widely been used as a fluorinated surfactant in aqueous film forming foams used as hydrocarbon fuel fire extinguishers. Due to concerns regarding its environmental persistence and toxicological effects, PFOS has recently been replaced by novel fluorinated surfactants such as Forafac®1157, developed by the DuPont company. The major component of Forafac®1157 is a 6:2 fluorotelomer sulfonamide alkylbetaine (6:2 FTAB), and a link between the trade name and the exact chemical structure is presented here to the scientific community for the first time. In the present work, the structure of the 6:2 FTAB was elucidated by ¹H, ¹³C and ¹⁹F nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry. Moreover, its major metabolites from blue mussel (Mytilus edulis) and turbot (Scophthalmus maximus) and its photolytic transformation products were identified. Contrary to what has earlier been observed for PFOS, the 6:2 FTAB was extensively metabolized by blue mussel and turbot exposed to Forafac®1157. The major metabolite was a deacetylated betaine species, from which mono- and di-demethylated metabolites also were formed. Another abundant metabolite was the 6:2 fluorotelomer sulfonamide. In another experiment, Forafac®1157 was subjected to UV-light induced photolysis. The experimental conditions aimed to simulate Arctic conditions and the deacetylated species was again the primary transformation product of 6:2 FTAB. A 6:2 fluorotelomer sulfonamide was also formed along with a non-identified transformation product. The environmental presence of most of the metabolites and transformation products was qualitatively demonstrated by analysis of soil samples taken in close proximity to an airport fire training facility.     

垃圾填埋场甲烷氧化菌及甲烷通量的研究

采用静态箱法、滚管计数法和气相色谱法,对6个不同封场时间填埋区的甲烷通量、覆土层甲烷氧化菌数量和甲烷氧化速率的变化趋势进行了测定,并分析了它们与封场时间、植被覆盖率等因素之间的相关性。结果发现6个填埋区甲烷通量的变化范围在-0.34～5.31 mg/(m2.h)之间;覆土层甲烷氧化菌的数量范围为3.10×107～20.77×107 cfu/g干土,甲烷氧化速率在1.65×10-8～4.34×10-8mol/(h.g)之间。覆土层甲烷氧化菌的数量与甲烷氧化速率呈正相关,但前者并不是后者的决定性因素;甲烷通量高时可刺激甲烷氧化菌数量及氧化速率的提高,且三者均与封场时间呈显著负相关,与植被覆盖率呈负相关;当含水率大于15%时,随着覆土层含水率的增加,甲烷氧化速率呈下降趋势;覆土pH、有机质和铵态氮与甲烷氧化速率等无明显相关性。提高覆土层的甲烷氧化速率可有效减少垃圾填埋场的甲烷排放。     

改进型波形潜流人工湿地处理猪场废水

提出了一种改进型波形潜流人工湿地(improved wavy subsurface flow constructed wetland,IW-SFCW)并研究了该湿地系统在5个水力停留时间(hydraulic retention time,HRT)(2、3、4、6和8 d)下对猪场废水的处理效果。结果表明,该湿地系统对猪场废水中各污染物有较好的去除效果。在水力停留时间为4 d,进水COD、TN、NH4+-N和TP浓度分别为511、120、110和10 mg/L左右时,该湿地系统对COD、TN、NH4+-N和TP的去除率分别为86.0%、54.4%、70.1%和91.6%。此外,该湿地系统对废水中COD、TP的去除效率随水力停留时间的延长逐渐提高,在HRT=8 d时去除效果最好,去除率分别达到92.7%和96.8%;但对TN、NH4+-N的去除率却随水力停留时间的延长出现先上升后下降的趋势,在HRT=4 d时去除率最高,分别为54.4%和70.1%。     

纳滤膜深度处理棉针织品印染废水

采用芳香聚酰胺膜(NF-1#)、复合膜(NF-2#)和聚酰胺复合膜(NF-3#)深度处理棉针织品印染废水,考察了膜分离性能及膜污染情况的影响因素。实验结果表明,在操作压力为0.5MPa、废水温度为25~35℃、废水pH为7的条件下,NF-1#膜处理效果最佳,COD去除率最高,为76.0%~85.0%;脱盐率也最高,达90.0%。膜过滤后浓水送污水厂处理,产水回用于车间生产。操作压力增高、废水温度升高和废水pH增大均导致滤饼层阻力(Rc)和膜过滤过程中的总阻力(Rt)增加,Rc是Rt的主要组成部分,同时也是导致膜透过通量下降的主要因素。     

实验室率定法测算长江南通段污染物降解系数

污染物降解系数是确定水环境容量的关键参数之一,本文采用实验室率定法,采集长江南通段的水样,分别于6℃、10℃、16℃、20℃室温下,在实验室内进行周期为20天的室内水质分析,根据室内水质分析结果,测算出不同温度下长江南通段"十二五"减排的约束性指标化学需氧量、氨氮的降解系数,并定性分析了长江水体中污染物本底浓度、可生化性、pH值等环境因子对污染物降解系数可能发生的影响。