化工废水治理措施综述

给出了从源头减少化工废水排放的一些控制措施;对于排放的废水,根据化工废水中有机物、含盐量、有毒特征污染物浓度的高低,色度的高低,将废水分为五类:并对国内近几年与文中分类相似的化工废水的末端治理工程措施进行了介绍;同时也罗列了废水回用和废水中有用原料回收的措施.     

阳离子表面活性剂十六烷基三甲基溴化铵对酞酸酯类化合物增溶性研究

用阳离子表面活性剂十六烷基三甲基溴化铵对六种酞酸酯类化合物(五种脂肪链酞酸酯和一种苯基酞酸酯)进行了增溶性实验．结果表明,在表观浓度(Ｃｓ)小于临界胶速浓度(ＣＭＣ)时,十六烷基三甲基溴化铵对四种酞酸酯(ＤＭＰ和ＤＰｈＰ除外)有一定程度的增溶作用;当Ｃｓ大于ＣＭＣ时,对六种化合物的增溶性显著增强．其增溶性(Ｓｔ/Ｓｗ)随Ｃｓ增大而线性递增:当Ｃｓ＜ＣＭＣ时,Ｓｔ/Ｓｗ＝ａ＋Ｋｍｎ·Ｃｓ,ｒ＞０．９０,ｎ＝５;当Ｃｓ＞ＣＭＣ时,Ｓｔ/Ｓｗ＝ａ＋Ｋｍｃ·Ｃｓ,ｒ＞０．９９,ｎ＝５． 各化合物增溶系数随各自固有水溶性(Ｓｗ)减小而增大(苯基酞酸酯有所反常),ｌｇＫｍｎ和ｌｇＫｍｃ与各自ｌｇｌ/Ｓｗ具有良好的线性正相关性．本文进一步对增溶机理进行了分析解释．     

指数平滑法在西安地面变形预测中的应用

首先详细介绍了指数平滑法及二次曲线指数平滑法的预测过程, 然后用它对西安市地裂引起的地面变形进行了预测。结果表明预测效果良好。同时, 文中指出了应用指数平滑法的一些优点及应注意的一些问题。     

控轧控冷型Q550高强钢高温后的力学性能试验研究∗

通过升温、降温及冷却后的常温静力拉伸试验,对控轧控冷型(TMCP)Q550高强钢高温后的力学性能展开试验研究,得到了经历200～900℃之间9个不同的过火温度及自然冷却与浸水冷却两种冷却方式后,钢材的表观特征、应力-应变关系与基本力学性能参数,包括弹性模量、屈服强度、抗拉强度及断后伸长率。结果表明,过火温度及冷却方式对TMCP型Q550钢材弹性模量的影响较小;过火温度超过600℃时,钢材高温后的屈服强度和抗拉强度开始折减;过火温度达到700℃后,钢材的应力-应变曲线皆无屈服平台,不同冷却方式的结果开始呈现差异:随过火温度升高,自然冷却后钢材的强度减小而断后伸长率增大,浸水冷却则相反,且二者差异愈加明显。将试验结果与文献结果对比,发现当过火温度超过700℃时,TMCP型Q550高强钢高温后的力学性能与调质型(QT)Q550高强钢存在差异,在经历较高的过火温度后,TMCP钢在自然冷却下的强度折减比QT钢严重,浸水冷却下的强度增长程度低于QT钢。     

Photo-polymerization of triclosan in aqueous solution induced by ultraviolet radiation

The formation of 2,8-dichlorodibenzo-p-dioxin and other harmful degradation products in the photo-degradation process of triclosan is of increasing concern. Here we worked on the identification of polymerized products at high triclosan concentration and on the mechanism of photoreaction. Five dimmers and two trimers of triclosan were detected by liquid chromatography-mass spectrum analysis. 2,8-dichlorodibenzo-p-dioxin was also identified by comparing with an authentic standard. Relatively low pH and high concentration favored the polymerization of triclosan. Three main routes of photoreaction were postulated, namely dechlorination, ring closure and polymerization.     

国家生态文明建设试点示范区指标合理性探讨

环保部于2013年5月23日颁布的《国家生态文明建设试点示范区指标（试行）》（以下简称《指标（试行）》）已实施有9个月。到目前为止,全国已有6批生态文明建设试点地区参照《指标》要求确定生态文明建设目标,编制生态文明规划。然而,实际工作中发现指标体系中部分指标的合理性有待商榷。本文通过对问题指标进行分类探讨,将指标存在的问题分为四大类：指标定义亟待完善、指标标准设定偏高、指标数据获取性差和参考标准有待更新。根据不同类型指标问题的特点,分别对指标进行分析并提出合理的改进和解决方案,为环保部对《指标（试行）》的进一步完善和改进提供了理论依据和思路,对我国生态文明建设工作持续健康发展起到了促进作用。     

多氯联苯对我国土壤微生物的生态毒理效应

作为持久性有机污染物(POPs),多氯联苯(PCBs)一旦进入土壤将长期存留并对土栖生物产生潜在危害。土壤微生物是土壤生态系统重要组成部分,研究外源PCBs对土壤微生物的生态毒理效应,筛选出指示PCBs污染的敏感指标并获取可靠的生态毒理数据十分重要。研究以江西红壤和天津潮土为供试土壤,在室内25℃连续培养28 d的条件下进行了生态毒理实验,选择了微生物量碳、呼吸强度、代谢熵、硝化作用、脱氢酶活性、脲酶活性和微生物群落功能多样性为微生物指标。结果显示:1)在28 d培养时间内,多氯联苯(PCBs)的毒性作用随培养时间的延长而增强,且在红壤中的毒性作用强于在潮土中,表明PCBs对土壤微生物的毒性作用存在时间效应并受土壤性质的影响。2)各微生物指标的敏感性不同,微生物量碳、脲酶活性和微生物功能多样性对PCBs污染反应不够敏感,而土壤呼吸强度、代谢熵、硝化作用和脱氢酶活性对PCBs污染反应敏感。3)14 d时,红壤中PCBs对脱氢酶活性、呼吸强度和代谢熵的EC10值分别为1.20、3.18和1.09 mg·kg-1,而在潮土中分别为6.31、4.73和50 mg·kg-1;28 d时,红壤中PCBs对硝化作用、脱氢酶活性、呼吸强度和代谢熵的EC10值分别为2.32、0.77、0.51和0.71mg·kg-1,而在潮土中分别为5.91、1.65、3.00和50 mg·kg-1。综合考虑经济和实际需要等因素,建议将呼吸强度、硝化作用和脱氢酶活性作为PCBs污染土壤生态毒理评价中的首选敏感指标,并建议培养时间设置为28 d。     

Indicating landfill stabilization state by using leachate property from Laogang Refuse Landfill

Variation and evolution process of leachate can be applied as a reference for landfill stabilization phase. In this work, leachates with different ages were collected from Laogang Refuse Landfill, and characterized with 14 key parameters. Simultaneously, principal component analysis （PCA） was applied to develop a synthetic parameter-F based on these 14 parameters, and a logarithm equation was simulated for the landfill stabilization process finally. It was predicted that leachates would meet Class I and Class II in standard for pollution control on the landfill site of municipal solid waste （GB 16889-1997） after 32 years and 22 years disposal under the natural attenuation in the humid and warm southern areas of China, respectively. The predication of landfill state would be more accurate and useful according to the synthetic parameter F of leachate from a working landfill.     

Influence of extracellular polymeric substances from activated sludge on the aggregation kinetics of silver and silver sulfide nanoparticles

• The NPs aggregation in the electrolyte solution is consistent with the DLVO theory. • In NaNO₃ and low Ca(NO₃)₂, EPS alleviates the NPs aggregation by steric repulsion. • In high Ca(NO₃)₂, EPS accelerates the NPs aggregation by exopolysaccharide bridging. • Ag₂S NPs have stronger stability compared with Cit-Ag NPs in aqueous systems. Extracellular polymeric substances (EPS) in activated sludge from wastewater treatment plants (WWTPs) could affect interactions between nanoparticles and alter their migration behavior. The influence mechanisms of silver nanoparticles (Ag NPs) and silver sulfide nanoparticles (Ag₂S NPs) aggregated by active EPS sludge were studied in monovalent or divalent cation solutions. The aggregation behaviors of the NPs without EPS followed the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory. The counterions aggravated the aggregation of both NPs, and the divalent cation had a strong neutralizing effect due to the decrease in electrostatic repulsive force. Through extended DLVO (EDLVO) model analysis, in NaNO₃ and low-concentration Ca(NO₃)₂ (<10 mmol/L) solutions, EPS could alleviate the aggregation behaviors of Cit-Ag NPs and Ag₂S NPs due to the enhancement of steric repulsive forces. At high concentrations of Ca(NO₃)₂ (10‒100 mmol/L), exopolysaccharide macromolecules could promote the aggregation of Cit-Ag NPs and Ag₂S NPs by interparticle bridging. As the final transformation form of Ag NPs in water environments, Ag₂S NPs had better stability, possibly due to their small van der Waals forces and their strong steric repulsive forces. It is essential to elucidate the surface mechanisms between EPS and NPs to understand the different fates of metal-based and metal-sulfide NPs in WWTP systems.