Toxicological characterization of the landfill leachate prior/after chemical and electrochemical treatment: A study on human and plant cells

In this research, toxicological safety of two newly developed methods for the treatment of landfill leachate from the Piškornica (Croatia) sanitary landfill was investigated. Chemical treatment procedure combined chemical precipitation with CaO followed by coagulation with ferric chloride and final adsorption by clinoptilolite. Electrochemical treatment approach included pretreatment with ozone followed by electrooxidation/electrocoagulation and final polishing by microwave irradiation. Cell viability of untreated/treated landfill leachate was examined using fluorescence microscopy. Cytotoxic effect of the original leachate was obtained for both exposure periods (4 and 24 h) while treated samples showed no cytotoxic effect even after prolonged exposure time. The potential DNA damage of the untreated/treated landfill leachate was evaluated by the comet assay and cytokinesis-block micronucleus (CBMN) assay using either human or plant cells. The original leachate exhibited significantly higher comet assay parameters compared to negative control after 24 h exposure. On the contrary, there was no significant difference between negative control and chemically/electrochemically treated leachate for any of the parameters tested. There was also no significant increase in either CBMN assay parameter compared to the negative control following the exposure of the lymphocytes to the chemically or electrochemically treated landfill leachate for both exposure periods while the original sample showed significantly higher number of micronuclei, nucleoplasmic bridges and nuclear buds for both exposure times. Results suggest that both methods are suitable for the treatment of such complex waste effluent due to high removal efficiency of all measured parameters and toxicological safety of the treated effluent.     

多孔镁铝复合氧化物对水溶液中Cr（VI）的吸附性能

摘要以镁盐、铝盐、纯碱和烧碱为原料制备了一种多孔镁铝复合氧化物（P—Mg3.1AlO4.6）,其比表面积、平均孔径和总孔容分别为206．3m2／g、8．961nm和0．4208cm3／g。研究了这种多孑L材料对水溶液中cr（VI）的吸附性能,在25～45qC时,静态吸附量为82．32～141．7mg／g;当初始浓度100mg／L、流速5mL／min、床层高度10cm和pH=6时,半穿透时间、半穿透吸附量和饱和吸附量分别为406rain、49．28ing／g和51．30Ing／g;拟合参数及误差分析表明,cr（Ⅵ）在P—M敬。AIO4.6上的静态吸附过程符合Freundlich等温方程式和伪二级动力学方程,Yoon·Nelson模型能很好地预测cr（Ⅵ）在P—Mg3.1A104.6上的动态穿透曲线。     

饮用水源突发性苯胺污染应急处理技术研究

分别从水样浓度、pH、反应时间、药剂投加量以及两者联用时的投加顺序等方面研究了粉末活性炭、高锰酸钾以及两者联合使用时对苯胺的去除效果.结果表明,当污染发生时,高锰酸钾和粉末活性炭联用处理技术是可行的;先投加粉末活性炭再加高锰酸钾处理比先投加高锰酸钾再投加活性炭的去除效果好;当水样pH在中性条件下,粉末活性炭和高锰酸钾联用处理技术的去除效果好;应急处理的反应时间是30 min.     

废LCD面板有机材料水热资源化产乙酸

LCD面板主要由附着偏光片及液晶等有机材料的玻璃面板构成。有机材料的去除及资源化利用是废LCD面板处理的第一步。在水热条件下对废LCD面板进行了降解产酸研究。研究考察了反应温度、反应时间、氧化剂用量、水用量及pH值等对水热产乙酸产率及选择性的影响。通过正交实验确定了水热产乙酸的最佳操作条件：反应温度325℃,反应时间5min,氧化剂（30％H2O2）0．6mL,用水量2mL,近中性环境（pH6-6．5去离子水）。此条件下,乙酸产率及选择性分别为68．83％及70．56％。结果表明,以废LCD面板有机材料为原料,采用水热技术进行产乙酸反应,可实现其资源化再利用。     

重庆市大气污染对锌材料腐蚀的经济损失分析

简要介绍了材料大气腐蚀经济损失的估算方法,并以2002年为基准年,选择了重庆市主城中心的6个功能区作为代表性区域,运用腐蚀破坏剂量响应函数和使用寿命计算公式对锌材料的腐蚀经济损失进行了定量估算.结果表明,由大气污染腐蚀破坏锌材料造成的年直接经济损失约为4061.7万元,约为同期GDP的0.1%.其中,干沉降对经济损失总量的贡献率在71%～99%之间,均值为92%.     

碳酸锶生产中"三废"综合利用研究

介绍了碳还原法生产碳酸锶过程中"三废"的主要成分;提出了用克劳斯燃烧法和吸收氧化法生产硫磺,用直接合成法和4级联合吸收法生产硫脲综合利用废气的途径;提出了2种治理废水方案,不仅达到脱硫、脱氮、降解有机物目的,而且还可得到硫磺、碳酸氢氨副产品;探讨了锶渣在砖、水泥的生产及公路工程建设中应用的可行性.     

SO2在碳钢初期大气腐蚀中的作用

通过自建的模拟大气腐蚀系统,借助金相显微镜、扫描电镜(SEM/EDX)、X-射线衍射(XRD)和x-射线光电子能谱(XPS),研究了SO2对碳钢初期大气腐蚀行为的影响,并进一步用原子力显微镜从更微观的角度观察了在SO2环境中初期阶段腐蚀形貌变化.研究结果表明:在SO2污染大气环境中,随SO2浓度的升高碳钢腐蚀加快.在体积分数为5×10(-6)SO2的大气环境中,碳钢和耐候钢表面腐蚀主要以条状物生长,随着SO2浓度的升高,腐蚀产物的形貌发生改变,在体积分数为5×10(-5)SO2的大气环境中,条状锈和胞状锈同时生长.在锈层中S元素以FeSO4·4H2O的形式存在,腐蚀产物中还有γ-FeOOH.SO2在初期阶段加速了碳钢的腐蚀,降低了碳钢的耐蚀性.     

柔性散粒材料静力及动力学性能实验研究

战场环境下单兵防常规炸弹爆炸抗震减震技术装备及器材,由于受经费投入、战场环境等因素影响,一直没有成功研制并得到装备.通过室内砂箱振动台震动模拟试验,测试了不同柔性散粒材料在震动条件下的加速度值,对其减震性能作了一些初步的探讨.通过研究,可以看到柔性散粒材料在隔震方面具有其他材料所不具有的优越性能,可以作为制造隔震器材的首选.     

Impacts on industry of Europe's emerging chemicals policy REACh

For Europe, a new regime in chemicals regulation is about to start. After the proposal of the European Commission concerning the Registration, Evaluation and Authorization of Chemicals (REACh) passed its readings in the European Parliament and some differences with the European Council of Ministers were resolved, the regulation will come into force in June 2007. This paper is focused on the question how serious the cost burdens for industry induced by REACh will be, and whether the New European Member States (NMS) which joined the European Union in May 2004 will be able to cope with the regulation. This evaluation has been done by assessing the legislative, administrative and economic framework in New Member States and by analysing real business cases in companies. The empirical showcase business impact studies are at the same time of interest for companies of EU-15 states, other European countries who may implement the regulation, and even for exporters of raw materials and chemicals outside Europe, who will also have to comply with REACh if they market in the European Community. The results give no indications that REACh adoption will bring significant drawbacks to companies in the NMS. The emerging regulation will bring challenges for individual companies, especially for small and medium-sized ones, but for the European chemical industry as a whole, there is no question that it will be able to cope with REACh burdens without losing its global competitiveness.