电化学氢自养与硫自养集成去除饮用水中的硝酸盐

研究了一种电化学氢自养与硫自养集成去除饮用水中硝酸盐的方法，将2种自养反硝化集成，既可减少以硫作为电子供体产生的SO4^2-，也可以使硫自养反硝化产生的H^ 作为电化学产氢的前驱物。同时，在硫自养段可不添加调pH的CaCO3，避免了出水的硬度升高。试验结果表明，在反应器的水力停留时间（HRT）为1．9－5h，最小电流相应为3－16mA时，NO3^--N去除率达90％以上，出水中NO3^--N和SO4^2-浓度分别低于3．0mg/L和170mg/L,NO2^--N未检出，硫段和电氢段出水pH值均维持在中性附近。     

制定恶臭物质排放标准的原则和方法

本文叙述了制定恶臭物质排放标准的技术原则、计算方法和公式.同时以天津为例,介绍了对恶臭排放标准计算公式中的主要参数选取及确定系数的方法经验.     

多环芳烃对海洋贝类多生物水平毒性效应的研究进展

多环芳烃类化合物(PAHs)是海洋中常见的一类持久性有机污染物,对海洋生态安全及海洋生物健康造成严重威胁。海洋贝类作为海洋生态毒理学研究的模式生物,其滤食性、固着性等生理特点使其对PAHs具有较高的生物蓄积能力,可以在不同生物水平产生一系列的毒性效应。本文综述目前PAHs在海洋贝类多种生物水平所造成的生物毒性效应及其检测方法的研究进展,重点从个体生理特征、组织结构、细胞毒性和基因毒性4个层次展开讨论,为更有效地利用海洋贝类这一模型生物,深入开展PAHs对海洋生物的致毒效应与机制研究提供思路与检测方法参考。     

水处理氧化还原过程的电动化学特性

以流动电流为参数,研究了水处理条件下氧化还原过程的电动化学特性.考察了水中KMnO_4及其与Mn~(2+),Fe~(2+)之间氧化还原作用的流动电流(SC)规律,探讨了氧化还原的初始条件、水处理环境、原水水质、氧化剂与还原剂的投加方式等对流动电流的影响.结果表明,水中约0.5mg·l~(-1)的KMnO_4可产生SC的峰值,而且当它与Mn~(2+)和Fe~(2+)经不同条件进行氧化还原作用时,可通过SC值的变化表现出更为明显的电动化学特性.     

电解法制备高效聚合絮凝剂的研究进展

本文从现代絮凝剂及其絮凝作用原理出发，系统阐述了电解合成高效聚合氯化铝的基本原理、现有方法以及尚存的关键理论和技术问题，并预计它能克服现有化学制备方法的局限性，提高产品质量，有着重要的科学意义，实用价值和广阔的应用前景。     

Degradation of azo dye Acid Red 14 in aqueous solution by electrokinetic and electrooxidation process

A new wastewater treatment technology--electrokinetic-electrooxidation process (EK-EO process) is developed in this paper. The EK-EO process can take advantage of both electrooxidation on the anode surface and the electrokinetic process of anionic impurities under an electric field, which can enhance the TOC removal in electrolysis process. The degradation of an anionic azo dye Acid Red 14 (AR14) was experimentally investigated. It was found that under an electric field AR14 could be migrated into anode compartment and be efficiently mineralized. After 360 min electrolysis of 100 mgl(-1) AR14 solutions at 4.5 mAcm(-2), complete discoloration was observed in both cathode and anode compartment. About 60% TOC was electromigrated from cathode compartment to anode compartment, and more than 25 mgl(-1) TOC was abated in anode compartment. A possible degradation mechanism of AR14 by EK-EO process was proposed. Additionally, the effect of current density, recycling flux, and electrolyte concentration on the EK-EO degradation of AR14 was also investigated.     

物理化学法处理垃圾填埋场渗滤液的研究进展

本文介绍了渗滤液的特性 ,指出物理化学法是渗滤液处理过程中不可缺少的环节。总结了物理化学法处理渗滤液的进展状况 ,并提出了物理化学法处理渗滤液存在的问题及未来发展趋势     

不同管材水管与静态自来水水质间的相互影响

对比了铝塑复合管(PAP)、铜管、不锈钢管和镀锌铁管对静态自来水的总有机碳(TOC)、溶解氧(DO)、浊度、细菌总数和大肠菌群等水质指标的影响。实验结果表明,铜管对自来水水质指标影响最小,且具有良好的卫生性能。同时,通过场发射扫描电子显微镜(FESEM)的观察,对比分析了铜管和铝塑复合管在浸泡实验前后其内表面形态特征的变化,结果显示自来水中浸泡10个月以后,铜管内表面密集地分布着块状的孔雀石晶体,而铝塑复合管内表面已严重变形,产生很多褶皱。     

几种无机混凝剂对酸性红染料的脱色研究

比较了无机混凝剂氯化铁、氯化铝和硫酸铝对染色废水的脱色效果，实验结果表明：氯化剂的絮凝脱色效果最佳，其适宜ｐＨ在２．５￣４．５之间，当加入适量的膨润土，则能拓宽ｐＨ适用范围，稳定脱色效果。     

Degradation of microcystins in aqueous solution with in situ electrogenerated active chlorine

A new and efficient method for the degradation of microcystins (one family of blue algal toxins) was developed and studied. Microcystins (MCs) in water were directly and effectively removed by active chlorine transformed in situ from the naturally existing Cl- in water resource using electrochemical method. Titanium coated with RuO2 and TiO2 was used as the anode. Microcystin-RR (MCRR) and Microcystin-LR (MCLR) were chosen as the model compounds of MCs. The results suggested that 20.87 mgl(-1) MCs (12.58 mgl(-1) MCRR and 8.29 mgl(-1) MCLR) in aqueous solution with 1.85 mM Cl- could be synchronously decomposed within 15 min electrolysis under the condition of the current density 8.89 mAcm(-2), 20 degrees C and pH 7.00. The qualitative analysis showed that the heptapetide ring and the Adda group of both treated MCs were changed. The results also indicated that the removal rates of both MCs increased with the increasing of chloride concentration and applied current density, but decreased with the increasing of initial concentration of MCs and initial pH of electrolyte. In the absence of Cl-, only a small fraction of both MCs were decomposed by direct anodic oxidation, while their almost complete removals could be obtained in the case of indirect electrooxidation with in situ electrogenerated active chlorine from Cl- in water.