城市污水净化的环境效益与环境影响分析

对佛山城市污水净化系统的环境响应和效益预测原则，城市污水净系统正式运转将对佛山水道化纤厂至人民桥段及佛山涌水质有明显改善，其社会效益十分显著，但净化系统的建设交将带来以恶臭、卫生防疫和噪声等方面为主的不利环境影响。因此在城市环境建设中应尽量减少城市污水净化的负面影响，充分发挥其环境效应和社会效益，为城市环境综合整治创造良好的条件。     

三种激光雷达监测污染物分布和输送对比

利用3种不同型号激光雷达在广州番禺大气成分观测站开展外场同步对比观测实验.通过全球地基气溶胶监测网（AERONET）气溶胶光学厚度（AOD）产品验证了3种激光雷达原始信号反演消光系数的可靠性.同时对比探讨了激光雷达低层反演能见度产品与能见度仪的相关性;对比美国国家环境预报中心全球同化系统模式（NCEP-GDAS）模拟结果讨论了激光雷达对混合层高度反演的有效性.最后利用个例分析揭示不同天气型下污染物可能的外源输送和本地积累.量化分析结果表明：3部激光雷达反演的能见度与能见度仪的相关系数均达到0.7以上,混合层高度均与NCEP-GDAS模式计算的混合层高度具有一定的可比性.与模拟结果相比,白天混合层高度在霾天气时相对较低,更能有效的揭示霾天气,亦可反映夜间间歇性湍流特性.应用分析表明：3部激光雷达均能较为一致的监测污染物的输送和本地的累积.外来输送主要以弱冷空气输送型为例,分析个例（2014年11月21~22日、24~25日）表明：后一过程（24~25日）由于夜间混合层高度（MLH）低,导致上层的粒子无法下传,污染物聚集在0.8km,且快速过境了,而前一过程（21~22日）整层输送,导致了近地层相对高的PM_2.5浓度;本地累积主要以冷高出海型为例（2014年11月25日20：00~27日20：00）,逆温与低的地表通风系数共同造成了前一时段（25日20：00~26日20：00）的消光明显高于后一时段（26日20：00~27日20：00）.     

大气气溶胶物质来源研究进展

大气气溶胶物质来源研究是大气污染研究极为重要的内容,它对污染物质的追踪评价具有较大的意义。本文较为系统地讨论了大气气溶胶物质来源研究的现状。从气溶胶的特征上分别论述气溶胶物质来源的矿物学（ 颗粒） 、无机化学和有机化学研究的进展。     

序言

正中国科学院资深院士、中国科学院广州地球化学研究所研究员、著名有机地球化学与沉积学家傅家谟先生离开我们已近一年,我们深沉缅怀他对地球科学、环境科学技术的卓越贡献。傅家谟院士1933年5月生于上海,原籍湖南沅江。1991年当选为中国科学院学部委员(院士)。1956年毕业于北京地质学院地质矿产系。1961年获中国科学院地质研究所硕士学位。曾任中国科学院地球化学研究所副所长、有机地球化学国家重点实验室主任、广东省环境资源利用与保护重点实验室主任,上海大学     

Occurrence of polychlorinated biphenyls (PCBs) together with sediment properties in the surface sediments of the Bering Sea, Chukchi Sea and Canada Basin

The spatial distribution and potential source of polychlorinated biphenyls (PCBs) in surface sediments from Bering Sea, Chukchi Sea, and Canada Basin and the relationship between PCBs and sedimentary properties including grain size, water content, loss on ignition, total organic carbon, and black carbon were explored. ΣPCBs (the sum of the detected PCB congeners) concentrations fluctuated in the study area, ranging from 22-150, 60-640 and 24-600 pg g(-1) dry weight for the Bering Sea, Chukchi Sea, and Canada Basin. A similar homologue pattern was observed at different locations, with tri-chlorinated PCBs being the dominant homologue, implying that the PCBs came mainly from the atmospheric transportation and deposition and ocean current transportation. No apparent co-relationships between PCB concentrations and sediment properties were obtained, indicating that the distribution of PCBs was not only controlled by their source, but also by the multi-factors such as atmospheric transport and depositing, mixing, partitioning and sorption in the water column and sediments.     

污泥回流比对厌氧/好氧工艺除磷效果影响的研究

以长距离输送的合流制污水为进水,考察不同污泥回流比下厌氧/好氧(A/O)工艺对COD、N、P的去除效果,深入研究污泥回流比对生物除P代谢过程的影响.结果表明,污泥回流比对COD及NH+4-N的去除没有明显影响,但对TN、TP、PO3-4-P的去除影响较大.随着污泥回流比的增大,聚磷菌(PAO)的厌氧释P量逐渐减小,P的去除率逐渐降低.减小污泥回流比,可延长A/O工艺厌氧池实际HRT,增加PAO在厌氧池可有效利用的碳源,使PAO在厌氧池充分释P,从而提高除P效率.     

Polybrominated diphenyl ethers in plastic products,indoor dust,sediment and fish from informal e-waste recycling sites in Vietnam: a comprehensive assessment of contamination,accumulation pattern,emissions, and human exposure

Residue concentrations of polybrominated diphenyl ethers (PBDEs) in different kinds of samples including consumer products, indoor dust, sediment and fish collected from two e-waste recycling sites, and some industrial, urban and suburban areas in Vietnam were determined to provide a comprehensive assessment of the contamination levels, accumulation pattern, emission potential and human exposure through dust ingestion and fish consumption. There was a large variation of PBDE levels in plastic parts of obsolete electronic equipment (from 1730 to 97,300 ng/g), which is a common result observed in consumer plastic products reported elsewhere. PBDE levels in indoor dust samples collected from e-waste recycling sites ranged from 250 to 8740 ng/g, which were markedly higher than those in industrial areas and household offices. Emission rate of PBDEs from plastic parts of disposed electronic equipment to dust was estimated to be in a range from 3.4 × 10^?7 to 1.2 × 10^?5 (year^?1) for total PBDEs and from 2.9 × 10^?7 to 7.2 × 10^?6 (year^?1) for BDE-209. Some fish species collected from ponds in e-waste recycling villages contained elevated levels of PBDEs, especially BDE-209, which were markedly higher than those in fish previously reported. Overall, levels and patterns of PBDE accumulation in different kinds of samples suggest significant emission from e-waste sites and that these areas are potential sources of PBDE contamination. Intakes of PBDEs via fish consumption were generally higher than those estimated through dust ingestion. Intake of BDE-99 and BDE-209 through dust ingestion contributes a large proportion due to higher concentrations in dust and fish. Body weight normalized daily intake through dust ingestion estimated for the e-waste recycling sites (0.10–3.46 ng/day/kg body wt.) were in a high range as compared to those reported in other countries. Our results highlight the potential releases of PBDEs from informal recycling activities and the high degree of human exposure and suggest the need for continuous investigations on environmental pollution and toxic impacts of e-waste-related hazardous chemicals.     

CO2 mineral sequestration in oil-shale wastes from Estonian power production

In the Republic of Estonia, local low-grade carbonaceous fossil fuel--Estonian oil-shale--is used as a primary energy source. Combustion of oil-shale is characterized by a high specific carbon emission factor (CEF). In Estonia, the power sector is the largest CO(2) emitter and is also a source of huge amounts of waste ash. Oil-shale has been burned by pulverized firing (PF) since 1959 and in circulating fluidized-bed combustors (CFBCs) since 2004-2005. Depending on the combustion technology, the ash contains a total of up to 30% free Ca-Mg oxides. In consequence, some amount of emitted CO(2) is bound by alkaline transportation water and by the ash during hydraulic transportation and open-air deposition. The goal of this study was to investigate the possibility of improving the extent of CO(2) capture using additional chemical and technological means, in particular the treatment of aqueous ash suspensions with model flue gases containing 10-15% CO(2). The results indicated that both types of ash (PF and CFBC) could be used as sorbents for CO(2) mineral sequestration. The amount of CO(2) captured averaged 60-65% of the carbonaceous CO(2) and 10-11% of the total CO(2) emissions.     

中国水资源利用效率评估及区域差异研究

水资源危机、水环境恶化已成为我国所面临的严峻挑战,对我国的水资源利用效率进行科学合理的评价,并且讨论造成区域差异的影响因素显得尤为迫切。在全要素生产框架下,将环境要素纳入到效率分析中,利用数据包络分析模型,采用省级层面统计数据,以资本、劳动力和水资源使用量为投入,以国内生产总值与废水排放量为产出,计算我国2000~2011年区域水资源利用效率。研究发现,在时间序列上,我国各省份之间的用水效率差距逐年增大;在空间上,我国的水资源利用效率存在明显的东、中、西部区域差异。进一步研究发现,产业结构、经济发展水平、水资源禀赋、水的基础设施投入对区域水资源利用效率均有显著影响,而水价并没有对水资源利用效率产生显著影响。     

铁炭微电解-Fe2+/K2S2O8降解甲基橙

针对偶氮类有机物废水具有色度大,难降解的特点,以对二甲基氨基偶氮苯磺酸钠(甲基橙)为模拟研究对象,对水体系中铁炭微电解-Fe2+/K2S2O8降解甲基橙的方法进行了研究。通过正交实验确定出该方法各因素的影响程度,进一步通过单因素影响实验确定该方法的最佳条件是:铁炭微电解填料、FeSO4和K2S2O8投加量分别为300 g/L、1.3mmol/L和0.7 mmol/L,初始pH值为7.0。在最佳条件下,甲基橙COD和色度去除率分别能达到64.7%和68.2%。