Recovery of solid fuel from municipal solid waste by hydrothermal treatment using subcritical water

Hydrothermal treatments using subcritical water (HTSW) such as that at 234 °C and 3 MPa (LT condition) and 295 °C and 8 MPa (HT condition) were investigated to recover solid fuel from municipal solid waste (MSW). Printing paper, dog food (DF), wooden chopsticks, and mixed plastic film and sheets of polyethylene, polypropylene, and polystyrene were prepared as model MSW components, in which polyvinylchloride (PVC) powder and sodium chloride were used to simulate Cl sources.While more than 75% of carbon in paper, DF, and wood was recovered as char under both LT and HT conditions, plastics did not degrade under either LT or HT conditions. The heating value (HV) of obtained char was 13,886-27,544 kJ/kg and was comparable to that of brown coal and lignite. Higher formation of fixed carbon and greater oxygen dissociation during HTSW were thought to improve the HV of char.Cl atoms added as PVC powder and sodium chloride to raw material remained in char after HTSW. However, most Cl originating from PVC was found to converse into soluble Cl compounds during HTSW under the HT condition and could be removed by washing.From these results, the merit of HTSW as a method of recovering solid fuel from MSW is considered to produce char with minimal carbon loss without a drying process prior to HTSW. In addition, Cl originating from PVC decomposes into soluble Cl compound under the HT condition. The combination of HTSW under the HT condition and char washing might improve the quality of char as alternative fuel.     

贵阳地区雨水化学与Sr同位素地球化学

对贵阳地区22个雨水样品的化学组成和Sr同位素的研究表明,贵阳地区大部分雨水样品的pH值小于56(pH=453).雨水中Ca2 是最主要的阳离子,平均值为57μmol·l-1(12—164μmol·l-1),占阳离子组成的64%—87%;Mg2 是次要的阳离子,平均值为13μmol·l-1(5—47μmol·l-1),Ca2 和Mg2 之和占了阳离子组成的78%—96%;K 平均值为11μmol·l-1(2—44μmol·l-1);Na 最少,其平均值为4μmol·l-1(1—8μmol·l-1).SO2-4是最主要的阴离子,平均值为94μmol·l-1(34—279μmol·l-1),占阴离子组成的28%—94%;NO-3是次要的阴离子,平均值为48μmol·l-1(1—252μmol·l-1),SO2-4和NO-3是决定雨水酸度最主要的离子,SO2-4和NO-3之和占阴离子组成的77%—99%;Cl-最少,平均值为20μmol·l-1(1—128μmol·l-1).贵阳地区雨水中Sr的浓度为002—033μmol·l-1,87Sr/86Sr比值较小(0707934—0709080),非海盐来源的87Sr/86Sr比值为0707820—0709078.元素比值及Sr同位素组成辨识出贵阳地区雨水溶质主要来源于人为活动,岩石/土壤化学风化次之,海相输入很小或可以忽略不计.     

大流量高流速溶洞堵漏技术的研究

在岩溶地区的各种工程的施工中,大流量、高流速溶洞的堵漏处理是一大难题。文章介绍了溶洞精确探测技术、堵漏材料、施工工艺上的最新研究成果,并以贵州猫跳河四级窄巷口水电站水库渗漏、贵州三岔河引子渡水电站厂房基坑涌水的处理为实例,介绍了孔间CT精确探测、模袋灌浆等技术的成功应用经验。     

居住小区雨水资源的利用与治理措施

徐州是严重缺水城市,水资源的匮乏催生了节水措施的开展。结合徐州市某居住小区环境影响报告书中的节水措施,分析其利用雨水资源的可行性和相应的治理措施。     

北京西北郊降尘和降雨中稀土元素的浓度分布和来源的初步分析

应用ICP－MS测定了从1998年10月至1999年9月共12个月的北京西北郊降尘中稀土元素的浓度，同时测定了从1999年4月至6月间8次降雨中的稀土元素的浓度，对降尘和降雨中稀土元素的分布模式进行了初步分析，结果表明降尘和降雨中稀土元素的分布与我国土壤稀土元素的分布模式基本一致，说明降尘和降雨中的稀土元素主要来源于地表土壤。     

贵州省赫章县土法炼锌过程中汞的释放量初步研究

对赫章县铅锌矿石、冶炼矿渣、煤、煤渣中汞含量进行了测定．结果表明,矿石中汞含量与锌含量存在显的正相关关系．基于上述测定结果并运用质量平衡法则,计算出不同类型矿石原料在冶炼过程中向大气的释汞因子：硫化矿为每生产It的Zn向大气释放155g的Hg;氧化矿为每生产It的Zn向大气释放79g的Hg．结合上述释放因子,对赫章土法炼锌过程中汞释放量进行了估算。     

北京市雨水资源综合利用与污染防治——迎绿色奥运,建生态北京

介绍了国内外雨水收集利用的情况,并针对北京水资源短缺和雨水资源大量浪费的现状,分析了北京市雨水资源收集和综合利用的前景,提出削减污染以及雨水综合利用的相关措施。北京天然雨水较清洁,然而经过在各种下垫面的冲刷后径流水质变差,初期径流污染物的含量相当大,甚至超过地表水环境质量标准的Ⅴ级。建议将初期降雨径流和后期雨水分开对待,将初期径流处理后再利用。     

雨水中S（Ⅳ）的离子色谱分析及其保护方法的研究

本文研究了用离子色谱法分析雨水中Ｓ（Ⅳ）的色谱条件和含Ｓ（Ⅳ）样品的保存方法，采用ＨＰＩＣ＿ＡＳＡ分离柱、用２ｍｍｏｌ．ｌ＾－１Ｎａ２ＣＯ３／３ｍｍｏｌ．ｌ＾０１ＮａＯＨ溶液作淋洗液、０．０１２５ｍｏｌ．ｌ＾－１Ｈ２ＳＯ４为再生液、电导检测的方法，具有无干扰和灵敏度高等优点，而且在Ｓ（Ⅵ）的浓度秋－２８μｇ．ｍｌ＾－１范围内，其浓度与响应值之间呈现出良好的线性关系，其线性相关系数在０．９９９５以上     

中国化工园区雨排系统环境风险防控研究

雨排系统是化工园区重要的基础设施,如果没有建立有效的环境风险防控体系,污染物有可能通过园区雨排系统排入外环境,造成重大环境影响.目前,中国已出台的有关化工园区雨排系统环境风险防控的政策法规缺少强制性和统一性,监管标准缺失导致环保部门缺乏行之有效的监管手段,园区规划阶段协同机制的不健全也增加了后期监管的难度.鉴于目前中国化工园区雨排系统环境风险防控方面存在的问题,建议国家和地方加快监管标准出台,强化相关政策的落实,优化园区雨排系统,实施分类、分级管控,同时加强企业的监管.     

Repeated batch and continuous degradation of chlorpyrifos by Pseudomonas putida

The present study was undertaken with the objective of studying repeated batch and continuous degradation of chlorpyrifos (O,O-diethyl O-3,5,6-trichloropyridin-2-yl phosphorothioate) using Ca-alginate immobilized cells of Pseudomonas putida isolated from an agricultural soil, and to study the genes and enzymes involved in degradation. The study was carried out to reduce the toxicity of chlorpyrifos by degrading it to less toxic metabolites. Long-term stability of pesticide degradation was studied during repeated batch degradation of chlorpyrifos, which was carried out over a period of 50 days. Immobilized cells were able to show 65% degradation of chlorpyrifos at the end of the 50th cycle with a cell leakage of 112 × 10³ cfu mL^?1. During continuous treatment, 100% degradation was observed at 100 mL h^?1 flow rate with 2% chlorpyrifos, and with 10% concentration of chlorpyrifos 98% and 80% degradation was recorded at 20 mL h^?1 and 100 mL h^?1 flow rate respectively. The products of degradation detected by liquid chromatography–mass spectrometry analysis were 3,5,6-trichloro-2-pyridinol and chlorpyrifos oxon. Plasmid curing experiments with ethidium bromide indicated that genes responsible for the degradation of chlorpyrifos are present on the chromosome and not on the plasmid. The results of Polymerase chain reaction indicate that a ~890-bp product expected for mpd gene was present in Ps. putida. Enzymatic degradation studies indicated that the enzymes involved in the degradation of chlorpyrifos are membrane-bound. The study indicates that immobilized cells of Ps. putida have the potential to be used in bioremediation of water contaminated with chlorpyrifos.