无机陶瓷膜处理冷轧厂乳化液废水工艺

通过对冷轧厂乳化液(含油)废水处理方法的对比,说明处理该废水采用无机陶瓷膜处理装置完全可行;介绍了无机陶瓷膜处理冷轧厂乳化液(含油)废水的工艺过程及处理系统组成。     

MBR技术的发展及应用

介绍了目前MBR的主要类型、膜污染情况、膜清洗方式以及MBR在不同领域的应用情况和工程实例,对MBR技术未来的发展趋势进行了预测。     

膜电解法在线再生酸性蚀刻液及回收铜新技术

采用极化曲线法研究了酸性蚀刻液阴、阳极电化学行为,并构建了离子膜电解反应体系,考察了在线再生酸性蚀刻液及回收铜的效果。结果表明,阳极氧化过程发生浓差极化,存在极限电流密度,Cu＋含量越高,极限电流密度越大;阴极还原分4步反应进行,存在极限电流密度;强化溶液传质可有效提高阴、阳极极限电流密度,有利于避免电解过程中析出氯气和氢气;在线实验表明,通过监控阳极液ORP,可避免析出氯气;分步降低电流电解有利于避免析出氢气,形成致密的金属铜块;在电流为9～24A范围内分4步电解23．5h可再生酸性蚀刻液23．5L,同时电沉积回收510g铜,纯度高达99．98％。阴极电流效率达到95．2％,吨铜电耗3251kWh。电解过程中无氯气和氢气析出,无废液排放,表明膜电解法在线再生酸性蚀刻液具有良好的应用前景。     

混凝剂品种对混凝-超滤联合工艺膜污染的影响

本实验以工业化学合成聚合硫酸铁混凝剂和自制生物聚合硫酸铁为例,考察了铁系混凝剂品种对地表水浊度、TOC和UV254的去除效果,混凝剂品种对混凝-超滤联合工艺处理地表水过程中超滤膜污染的影响。混凝实验结果表明,在10 mg/L(以Fe3+计)最佳投加量下,两类混凝剂对浊度、TOC和UV254的去除率基本相同。超滤膜污染实验结果表明,生物聚合铁预处理水样通量衰减速度略大于化学聚合铁预处理水样;膜污染阻力分析结果显示,随着循环次数的增加,工业化学合成聚合铁预处理水样造成的不可逆污染阻力逐渐增加,而生物聚合铁预处理水样造成的不可逆污染阻力却略有下降;膜污染机理分析表明,2组过滤过程的膜污染类型基本相似,由最初的膜孔堵塞过渡到最终的滤饼层污染。SEM分析表明,生物聚合铁预处理水样的膜污染较为严重。     

无机陶瓷膜处理油田采出水

针对陶瓷膜在油田采出水处理过程中操作参数的选择及污染机理进行了研究。通过现场实验,分析了不同的操作参数对膜通量的影响,陶瓷膜对含油量及悬浮物的去除效果,膜阻力组成及膜污染清洗方法。实验结果表明,在确定出水水质达到低渗透油田注水水质A1级标准条件下,陶瓷膜过滤最佳操作条件为:跨膜压差0.16 MPa、温度50℃、膜面流速5.0 m/s。同时发现,NaOH和HNO3联合清洗有助于恢复膜通量。     

乳状液膜法处理煤制兰炭废水

以磷酸三丁酯(TBP)为载体、煤油为膜溶剂、NaOH水溶液为内水相,采用乳状液膜法处理兰炭废水。实验结果表明:当TBP体积分数为4%、表面活性剂质量分数为4%、内水相NaOH质量分数为12%、油内比(乳状液的油相与内水相的体积比)为3∶2、乳水比为1∶5、萃取时间为15min时,废水中的酚类(以苯酚计)去除率达到85%以上,COD去除率达83%以上。     

Mobile passive samplers: concept for a novel mode of exposure

Integrative passive sampling with devices such as semipermeable membrane devices generally relies on rigs for month-long static exposures in water. We evaluate here whether mobile exposures of passive samplers can provide reliable estimates of dissolved contaminant concentrations. Mobile exposures were obtained by towing samplers fastened to the end of a benthic trawl net. Significant and reproducible absorption of polycyclic aromatic hydrocarbons during 5 h-long deployments was made possible by high sampling rates resulting from high water turbulences during towing at 1.2-1.5 knots. Sampling rates (72-215 L d⁻¹) estimated from the dissipation of performance reference compounds were supported by in situ calibration with samplers exposed for a 30 days in the vicinity of the test site. Higher fluoranthene and pyrene absorption in samplers exposed to the trawling-induced sediment plume could be attributed to desorption from re-suspended sediments. This mode of exposure has the potential to be used in monitoring programmes.     

电镀综合废水对DF膜的污染

江苏某电镀厂的电镀综合废水在采用DF膜进行预处理时,膜易受到污染。针对这一问题,采用DF膜生产厂家提供的小试装置,研究探索了膜污染的原因及其具体特征。实验结果表明,在处理电镀综合废水时,DF膜的污染速率较快,而酸洗对DF膜的恢复性较好,研究还证实电镀综合废水中的无氰沉锌水洗液是造成DF膜污染的主要原因。     

Determination of organochlorine and organophosphate pesticide residues in fruits,vegetables and sediments

Abstract

A method is described for the determination of organochlorine and organophosphate pesticide residues in fruits, vegetables and sediments. The concentrated solvent extract was sealed in a polymeric membrane tube, dialysed in cyclohexane and the solvent replaced with hexane. The organophosphates were analysed on a specific thermionic detector without further clean‐up. For the organochlorine pesticides the extract was eluted through 3 g of alumina and analysed on GC/ECD. The clean‐up for sediment extract was carried out on a10 g alumina column with 100 mL hexane containing 5% acetone and the eluate was concentrated to 5 mL.

The detection limit for organophosphates on a 40 g sample and a final volume of 10 mL was on the average 0.01 mg/kg. The detection limit for organochlorine pesticides, with the final volume of 25 mL, was 0.005 mg/kg for all pesticides except for p,p'‐DDT and endosulfan sulphate, which was 0.01 mg/kg.

The detection limit for oganochlorine pesticides in sediment, with the final volume of 2 mL, was less than 1 μg/kg and for organophosphate pesticides less than 10 μg/kg when the final volume was made to 0.5 mL. At the detection limits the method produced a very high coefficient of variation for both organochlorine and organophosphate pesticides.     

膜生物反应器废水处理新工艺

概述了国内外膜生物反应器的研究与应用状况；介绍了其构形与特点；分析了膜污染的成因，影响因素及防制措施；指出了今后的研究方向。