从醇/酮装置酸性废水中回收甲酸

采用共沸—分馏组合法从环己醇和环己酮生产装置产生的酸性废水中回收甲酸,确定了适宜挟带剂的种类及加入量。采用共沸—分馏组合法可获得甲酸质量分数达80%以上的甲酸水溶液,甲酸回收率达70%以上。回收甲酸后,酸性废水的COD由1.0×105~1.6×105m g/L降至500m g/L以下,COD去除率达到99%以上。     

Sorbents for CO2 capture from high carbon fly ashes

Fly ashes with high-unburned-carbon content, referred to as fly ash carbons, are an increasing problem for the utility industry, since they cannot be marketed as a cement extender and, therefore, have to be disposed. Previous work has explored the potential development of amine-enriched fly ash carbons for CO(2) capture. However, their performance was lower than that of commercially available sorbents, probably because the samples investigated were not activated prior to impregnation and, therefore, had a very low surface area. Accordingly, the work described here focuses on the development of activated fly ash derived sorbents for CO(2) capture. The samples were steam activated at 850 degrees C, resulting in a significant increase of the surface area (1075m(2)/g). The activated samples were impregnated with different amine compounds, and the resultant samples were tested for CO(2) capture at different temperatures. The CO(2) adsorption of the parent and activated samples is typical of a physical adsorption process. The impregnation process results in a decrease of the surface areas, indicating a blocking of the porosity. The highest adsorption capacity at 30 and 70 degrees C for the amine impregnated activated carbons was probably due to a combination of physical adsorption inherent from the parent sample and chemical adsorption of the loaded amine groups. The CO(2) adsorption capacities for the activated amine impregnated samples are higher than those previously published for fly ash carbons without activation (68.6 vs. 45mg CO(2)/g sorbent).     

微波-改性活性炭-Fenton试剂氧化法降解水中2,4-二氯酚

以经Fe2（SO4）3溶液浸渍改性的活性炭作催化剂、Fenton试剂作氧化剂,采用微波-改性活性炭-Fenton试剂氧化法降解水中的2,4-二氯酚。考察了改性活性炭加入量、H2O2与Fe^2＋摩尔比、Fenton试剂加入量、微波功率和2,4-二氯酚溶液初始pH对2,4-二氯酚降解效果的影响。在改性活性炭加入量1．0g／L、n（H2O2）：n（Fe^2＋）=16．7（H2O2加入量6．0mmol／L、Fe^2＋加入量0．36mmol／L）、Fenton试剂加入量为6．36mmol／L、微波功率600W、微波辐射时间10min、2,4-二氯酚溶液初始pH为6．0的条件下,2,4-二氯酚降解率和TOC去除率分别可达98．7％和84．0％。     

Paired assistance policy and recovery from the 2008 Wenchuan earthquake: a network perspective

The role of the paired assistance policy (PAP) in facilitating recovery after the Wenchuan earthquake in China on 12 May 2008 is best analysed from a network perspective. This paper makes five assumptions to explore the relationship, and then draws on three additional cases to examine them. The key findings support all five assumptions. First, the interactions of authority compliance initiated the PAP, and second, the interactions of resource input significantly contributed to rapid reconstruction following the earthquake. Third, the interactions of knowledge transfer supported social system recovery, and fourth, the interactions of benefit reciprocity laid the foundation for sustainable recovery. Fifth, by contrast, the interactions of performance comparison caused suboptimal overfunding of particular public infrastructure projects and reduced local self‐reliance to some extent. Finally, suggestions are made to improve the policy implications of extending the use of the PAP in other administrative contexts. The PAP could become an even more important policy device in the future.     

Control strategies for disinfection byproducts by ion exchange resin,nanofiltration and their sequential combination

● Effects of AER adsorption and NF on DBP precursors, DBPs, and TOX were examined. ● A treatment approach of resin adsorption followed by nanofiltration was developed. ● Both DOC and Br⁻ could be effectively removed by the sequential approach. ● DBPs, TOX, and cytotoxicity were significantly reduced by the sequential approach. Disinfection byproducts (DBPs) are emerging pollutants in drinking water with high health risks. Precursor reduction before disinfection is an effective strategy to control the formation of DBPs. In this study, three types of anion exchange resins (AERs) and two types of nanofiltration (NF) membranes were tested for their control effects on DBP precursors, DBPs, and total organic halogen (TOX). The results showed that, for AER adsorption, the removal efficiencies of DBP precursors, DBPs, and TOX increased with the increase of resin dose, and the strong basic macroporous anion exchange resin (M500MB) had the highest removal efficiencies. For NF, the highest removal efficiencies were achieved at an operating pressure of 4 bar, and the membrane (NF90) with a smaller molecular weight cut-off, had a better control efficiency. However, AER adsorption was inefficient in removing dissolved organic carbon (DOC); NF was inefficient in removing Br⁻ resulting in insufficient control of Br-DBPs. Accordingly, a sequential approach of AER (M500MB) adsorption followed by NF (NF90) was developed to enhance the control efficiency of DBPs. Compared with single AER adsorption and single NF, the sequential approach further increased the removal efficiencies of DOC by 19.4%–101.9%, coupled with the high Br⁻ removal efficiency of 92%, and thus improved the reduction of cyclic DBPs and TOX by 3.5%–4.9%, and 2.4%–8.4%, respectively; the sequential approach also reduced the cytotoxicity of the water sample by 66.4%.     

光子相关光谱（PCS）在无机高分子絮凝剂形态表征中的应用

本文运用现代先进的微粒检测手段光子相关光谱对常见的两类无机高分子絮凝剂的形态进行了表征。实验结果表明：在所测聚合氯化铁溶液中，体系呈较为单一的集中分布，由平移扩散系数计算得到平均有效直径在５－１１ｎｍ左右。在所测聚合氯化铝溶液中，主要为双峰分布，熟化后样品约为２－５ｎｍ的小颗粒与数十ｎｍ以上分布较宽的聚集体，另外，本文对光子相关光谱在形态表征中的优缺点及其它应用的可能性也作了一定的论述。     

聚合氯化铝与传统混凝剂的凝聚—絮凝行为差异

本文综合阐述无机高分子絮凝剂与传统混凝剂在化学特征和凝聚－絮凝行为机理上的差异。ＰＡＣ的主要成分聚十三铝在预制条件下能大量生成。它们对水解反应有一定的稳定性，直接吸附有颗粒物表面，发挥强烈的电中和及粘结架桥作用，其流动电流，ζ电位，絮凝指数及凝聚－絮凝区域图等，均与传统混凝剂有很大不同，其计算模式应根据表面络合及表面沉淀原理建立。     

城郊森林区对城区环境生态影响

城郊森林区正成为城市生态绿地系统的重要组成部分，本文选定常熟市及近郊的虞山国家森林公园作为实验区，根据主要环境影响因子的测试结果，分析探讨城郊森林区对城市区域的生态影响及作用机制，表明森林群落是优于其它下垫面类型的多层，多效，可持续利用的城区环境生物净化器。     

内蒙古草原生态环境治理的国际合作思路

内蒙古草原面积巨大,占全国草原总面积的1/3,其草原生态环境不仅与国家生态安全紧密相连,而且对周边国家的气候、环境也会产生重大影响。本文从国际法视角出发,根据国际合作原则,依据《京都议定书》清洁能源机制,提出了内蒙古草原生态治理的国际合作思路。一要依托联合国及联合国环境规划署,开展更为广泛的环保合作项目;二要依托国际社会各种环境保护组织和环境合作机构,在《联合国气候框架公约》和《京都议定书》等国际法框架内,全面开展环境外交,寻求国际社会的多方合作;三要依托内蒙古绿色食品贸易,与环境大国展开国际合作;四要依托内蒙古绿色能源基地的建设,寻求国际合作,希望本文能对政府部门制定草原生态治理规划时有所启迪和帮助。     

The effect of chlorine position of chlorinated phenols on their dechlorination kinetics by Fenton's reagent

Chlorine position of chlorophenol isomers has a significant effect on the dechlorination kinetics of monochlorophenols, dichlorophenols, and trichlorophenols during Fenton oxidation. The effects have been evaluated by the rate constants of the dechlorination kinetic model developed in this study. It is found that the dechlorination rate of 3-CP is faster than that of 4-CP, which is faster than that of 2-CP. Since OH and Cl groups on the aromatic ring are ortho and para directors, the directory effect of OH and Cl groups enhances the dechlorination kinetics of 2-CP due to acceleration of the hydroxylation of 2-CP. Therefore, the dechlorination kinetics increases accordingly. For trichlorophenols (TCP), steric hindrance plays an important role during their dechlorination process. Specifically, the closer the chlorine atoms locate with each other on the aromatic ring, the more difficult the dechlorination processes will be. The dechlorination kinetics of dichlorophenols seems to be affected by both directory effect of OH and Cl groups and the effect of steric hindrance of chlorine atoms. The directory effect of OH and Cl groups on trichlorophenols decreases since the chlorine atom occupied the positions which are the most favorable for hydroxyl radical attack.