废旧塑料污染的防治途径

本文简要介绍了废旧塑料的几种处理和再利用方法，以及控制其污染和采用这些方法应采取的对策意见。     

我国废水处理设备的现状及发展趋势

本文在调查的基础上，阐述了我国水处理设备的现状及技术发展趋势．并提出在符合国情的条件下，为取得更大的环境及经济效益，应优先发展高效、低耗、技术先进的产品．     

有机染料废水处理研究进展

对有机染料废水的物化处理法（混萃取、吸附、电解、膜分离、蒸馏浓缩及焚烧法）和生化法的特点及进展，特别对湿式氧化、光氧化，Ｆｅｎｔｏｎ试剂氧化，臭氧氧化法的研究进展作了重点阐述。     

用凹凸棒石处理高浓含油废水的研究

研究了凹凸棒石吸附剂(包括其回收再生品)对废水中各种状态油的去除,结果表明,1％凹凸棒石原土与1mg/LPAM组合,可使含油约500mg/L的废水获得90%以上的除油率;若组合使用2.00%凹凸棒石和800mg/L硫酸铝,则易使含油126000mg/L的废乳化液破乳除油,除油率均达98％左右,COD_(Cr)去除率89％:如采用多级连续处理,则可有效地净化水质;油的去除效果是凹凸棒石投加量或初始油浓度的幂函数,且在剩余油量与投加量之间符合Freundlich吸附等温式:整个吸附过程具有不同特征的几个阶段,并随着时间的推延,逐渐呈现一级反应动力学的特征。     

废旧轮胎热解资源化研究

废旧轮胎热解资源化是近年来世界各国关注的热点。热解温度控制在４００～８００℃便能得到燃料油、炭黑、钢丝和燃料气。热解工艺简单，操作方便，投产１８个月能收回全部投资，经济效益可观，同时减轻废旧轮胎对环境的压力。废旧轮胎必将成为一种既有能源价值，更有资源价值的新兴资源，补充世界各国对资源的需求。     

美国自来水行业消毒现状和展望

为了了解美国自来水行业消毒现状,在查阅了相关外文文献的基础上,对相关资料进行总结和分析.结果表明:氯气虽然仍是最广泛使用的消毒方式,但出于人们对健康安全的关注和许多饮用水法规的实施,使用氯气的水厂数量在不断减少.     

微波消解预处理测定水和废水中总磷

提出一种用微波消解技术作为测定水和废水中总磷的预处理方法，这种消解方法只需10min即可，比用常规的高温高压消解法节省三分之一时间。用这身份种消解法对标样、地表水、海水、生活污水和工业废水样品进行了对比测定，所得结果经统计检验，两方法之间无显著性差异。对微波消解法的精密度和准确度进行了验证。     

Waste activated sludge hydrolysis and acidification: A comparison between sodium hydroxide and steel slag addition

Alkaline treatment with steel slag and NaOH addition were investigated under different pH conditions for the fermentation of waste activated sludge. Better performance was achieved in steel slag addition scenarios for both sludge hydrolysis and acidification. More solubilization of organic matters and much production of higher VFA (volatile fatty acid) in a shorter time can be achieved at pH 10 when adjusted by steel slag. Higher enzyme activities were also observed in steel slag addition scenarios under the same pH conditions. Phosphorus concentration in the supernatant increased with fermentation time and pH in NaOH addition scenarios, while in contrast most phosphorus was released and captured by steel slag simultaneously in steel slag addition scenarios. These results suggest that steel slag can be used as a substitute for NaOH in sludge alkaline treatment.     

Rapid adsorption of toxic Pb(Ⅱ) ions from aqueous solution using multiwall carbon nanotubes synthesized by microwave chemical vapor deposition technique

Multiwall carbon nanotubes(MWCNTs) were synthesized using a tubular microwave chemical vapor deposition technique, using acetylene and hydrogen as the precursor gases and ferrocene as catalyst. The novel MWCNT samples were tested for their performance in terms of Pb(Ⅱ)binding. The synthesized MWCNT samples were characterized using Fourier Transform Infrared(FT-IR), Brunauer, Emmett and Teller(BET), Field Emission Scanning Electron Microscopy(FESEM) analysis, and the adsorption of Pb(Ⅱ) was studied as a function of p H,initial Pb(Ⅱ) concentration, MWCNT dosage, agitation speed, and adsorption time, and process parameters were optimized. The adsorption data followed both Freundlich and Langmuir isotherms. On the basis of the Langmuir model, Qmaxwas calculated to be 104.2 mg/g for the microwave-synthesized MWCNTs. In order to investigate the dynamic behavior of MWCNTs as an adsorbent, the kinetic data were modeled using pseudo first-order and pseudo second-order equations. Different thermodynamic parameters, viz., ΔH0, ΔS0and ΔG0were evaluated and it was found that the adsorption was feasible, spontaneous and endothermic in nature. The statistical analysis revealed that the optimum conditions for the highest removal(99.9%) of Pb(Ⅱ) are at p H 5, MWCNT dosage 0.1 g, agitation speed 160 r/min and time of 22.5 min with the initial concentration of 10 mg/L. Our results proved that microwave-synthesized MWCNTs can be used as an effective Pb(Ⅱ) adsorbent due to their high adsorption capacity as well as the short adsorption time needed to achieve equilibrium.     

Nontargeted identification of peptides and disinfection byproducts in water

A broad range of organic compounds are known to exist in drinking water sources and serve as precursors of disinfection byproducts(DBPs).Epidemiological findings of an association of increased risk of bladder cancer with the consumption of chlorinated water has resulted in health concerns about DBPs.Peptides are thought to be an important category of DBP precursors in water.However,little is known about the actual presence of peptides and their DBPs in drinking water because of their high sample complexity and low concentrations.To address this challenge and identify peptides and non-chlorinated/chlorinated peptide DBPs from large sets of organic compounds in water,we developed a novel high throughput analysis strategy,which integrated multiple solid phase extraction(SPE),high performance liquid chromatography(HPLC)separation,and non-target identification using precursor ion exclusion(PIE)high resolution mass spectrometry(MS).After MS analysis,structures of candidate compounds,particularly peptides,were obtained by searching against the Human Metabolome Database(HMDB).Using this strategy,we successfully detected 625 peptides(out of 17,205 putative compounds)and 617 peptides(out of 13,297)respectively in source and finished water samples.The source and finished water samples had 501 peptides and amino acids in common.The remaining 116 peptides and amino acids were unique to the finished water.From a subset of 30 putative compounds for which standards were available,25 were confirmed using HPLC-MS analysis.By analyzing the peptides identified in source and finished water,we successfully confirmed three disinfection reaction pathways that convert peptides into toxic DBPs.