A strategy for aromatic hydrocarbon bioremediation under anaerobic conditions and the impacts of ethanol: a microcosm study

Increased use of ethanol-blended gasoline (gasohol) and its potential release into the subsurface have spurred interest in studying the biodegradation of and interactions between ethanol and gasoline components such as benzene, toluene, ethylbenzene and xylene isomers (BTEX) in groundwater plumes. The preferred substrate status and the high biological oxygen demand (BOD) posed by ethanol and its biodegradation products suggests that anaerobic electron acceptors (EAs) will be required to support in situ bioremediation of BTEX. To develop a strategy for aromatic hydrocarbon bioremediation and to understand the impacts of ethanol on BTEX biodegradation under strictly anaerobic conditions, a microcosm experiment was conducted using pristine aquifer sand and groundwater obtained from Canadian Forces Base Borden, Canada. The initial electron accepter pool included nitrate, sulfate and/or ferric iron. The microcosms typically contained 400 g of sediment, 600 approximately 800 ml of groundwater, and with differing EAs added, and were run under anaerobic conditions. Ethanol was added to some at concentrations of 500 and 5000 mg/L. Trends for biodegradation of aromatic hydrocarbons for the Borden aquifer material were first developed in the absence of ethanol, The results showed that indigenous microorganisms could degrade all aromatic hydrocarbons (BTEX and trimethylbenzene isomers-TMB) under nitrate- and ferric iron-combined conditions, but not under sulfate-reducing conditions. Toluene, ethylbenzene and m/p-xylene were biodegraded under denitrifying conditions. However, the persistence of benzene indicated that enhancing denitrification alone was insufficient. Both benzene and o-xylene biodegraded significantly under iron-reducing conditions, but only after denitrification had removed other aromatics. For the trimethylbenzene isomers, 1,3,5-TMB biodegradation was found under denitrifying and then iron-reducing conditions. Biodegradation of 1,2,3-TMB or 1,2,4-TMB was slower under iron-reducing conditions. This study suggests that addition of excess ferric iron combined with limited nitrate has promise for in situ bioremediation of BTEX and TMB in the Borden aquifer and possibly for other sites contaminated by hydrocarbons. This study is the first to report 1,2,3-TMB biodegradation under strictly anaerobic condition. With the addition of 500 mg/L ethanol but without EA addition, ethanol and its main intermediate, acetate, were quickly biodegraded within 41 d with methane as a major product. Ethanol initially present at 5000 mg/L without EA addition declined slowly with the persistence of unidentified volatile fatty acids, likely propionate and butyrate, but less methane. In contrast, all ethanol disappeared with repeated additions of either nitrate or ferric iron, but acetate and unidentified intermediates persisted under iron-enhanced conditions. With the addition of 500 mg/L ethanol and nitrate, only minor toluene biodegradation was observed under denitrifying conditions and only after ethanol and acetate were utilized. The higher ethanol concentration (5000 mg/L) essentially shut down BTEX biodegradation likely due to high EA demand provided by ethanol and its intermediates. The negative findings for anaerobic BTEX biodegradation in the presence of ethanol and/or its biodegradation products are in contrast to recent research reported by Da Silva et al. [Da Silva, M.L.B., Ruiz-Aguilar, G.M.L., Alvarez, P.J.J., 2005. Enhanced anaerobic biodegradation of BTEX-ethanol mixtures in aquifer columns amended with sulfate, chelated ferric iron or nitrate. Biodegradation. 16, 105-114]. Our results suggest that the apparent conservation of high residual labile carbon as biodegradation products such as acetate makes natural attenuation of aromatics less effective, and makes subsequent addition of EAs to promote in situ BTEX biodegradation problematic.     

含锌多核聚铝絮凝剂的制备及形态特征

以AlCl3·6H2O和ZnCl2为原料,采用一次加碱法制备了一种新型的改性增效聚合铝类多核无机高分子絮凝剂聚合氯化铝锌(PAZC).通过Al-Ferron逐时络合比色法研究了碱化度(B),Al/Zn摩尔比及陈化时间对铝离子形态的影响.采用混凝实验比较PAZC、PAC的混凝效果.结果表明:在相同B值条件下,PAZC的Ala和Alc少于PAC的Ala和Alc,Alb形态多于PAC中Alb形态,并且PAC中Alb形态最高只有60%,而PAZC中Alb最高达到83%.PAZC具有pH适用范围宽,投药量少以及良好的储存性能.     

污水厂污泥一体化竖式强化渗滤浓缩自然干化与消化研究

针对目前国内污泥处理处置存在的问题,为实现污泥浓缩消化一体化,开发了污泥一体化强化渗滤浓缩自然干化与消化新工艺反应器,并进行了城市水厂污泥处理试验.结果表明,在有机负荷为0.8 kg VSS/(m3·d)、平均水力停留时间为8.3 d、污泥停留时间为120 d的条件下,污泥有机物去除率可达到44.4%,排泥含水率达到79.1%,污泥消化与浓缩过程起到了相互促进的作用.渗滤液须抽回至污水处理厂处理.     

基于BP神经网络的垃圾焚烧过程故障诊断

应用BP神经网络方法,建立了垃圾焚烧过程故障诊断的模型.该方法采用梯度下降法训练网络权值,利用最优停止法对网络进行了优化,避免了过拟合现象.提高了BP神经网络的训练速度和泛化能力.并以实际焚烧过程工况数据进行性能检验,检验结果表明了该BP网络具有较高的诊断精度.     

QUAL2K模型在西苕溪干流梅溪段水质模拟中的应用

QUAL2K是一维稳态水质模型,由美国环保局开发并在QUAL2E模型的基础上发展起来的.采用QUAL2K模型对西苕溪干流梅溪段的水质进行了模拟和预测.针对西苕溪的具体情况,选用COD、氨氮和总磷作为模拟预测指标,用模型率定法并参考相关文献确定了COD降解系数Kc、氨氮降解系数Kn和总磷平衡系数Kp等水质参数,并对模拟结果进行了验证,结果表明预测值和实测值的相关性较好.     

应用陶粒过滤-陶瓷膜组合对止咳糖浆制药废水深度处理的试验研究

止咳精浆制药废水经生物接触氧化一体化废水处理装置处理后,其出水中COD、BOD和氨氮等主要污染物质均不能达标排放.在实验室中采用陶粒过滤-陶瓷膜组合对经一体化处理装置处理后的制药废水进行深度处理,在陶粒柱反应器选用粒径为1～2 mm的陶粒滤料,陶瓷膜反应器选用孔径为2～3/μm陶瓷膜的条件下对水样进行测试.废水经陶粒过滤-陶瓷膜组合处理后,其BOD、COD、SS和氨氮指标均可稳定达标排放.     

溶胶凝胶法制备磷钨酸掺杂TiO2薄膜及其光催化性能

以钛酸四丁酯为前驱物,采用溶胶凝胶法制备了磷钨酸掺杂的二氧化钛薄膜.通过XRD、FT-TR对该薄膜进行了表征,研究了薄膜在对氯苯酚光降解中的催化活性.结果表明,当磷钨酸与二氧化钛摩尔比为0.01:1、薄膜烧结温度600℃、对氯苯酚溶液浓度30 mg/L(pH＝5)、光催化8 h的条件下,对氯苯酚的降解率超过90%,且薄膜可以重复使用.磷钨酸对二氧化钛的光催化活性具有明显的促进作用.     

劳动力外出务工对承灾体恢复力的影响——以河北省邢台县旱灾调查为例

农村劳动力资源是构成农户承灾体恢复力的重要因素.一般认为农村劳动力外出务工,可以提高农户家庭的经济水平,进而提升农户的旱灾恢复力.通过对河北省邢台县的实地调查研究发现,劳动力外出务工与农户承灾体恢复力间存在着微妙的关系.研究表明,户主外出务工模式不仅在农业生产的灾后恢复上,而且在农户家庭经济的恢复上均有积极的意义.对于子女外出务工家庭而言,子女不愿意再从事农业生产,并且子女的务工收入对家庭的贡献十分有限,即子女外出务工对家庭旱灾恢复力影响较小.     

四川汶川8．0级地震典型遗址遗迹综合评估

简要介绍了四川汶川8.0级地震现场考察的有关情况,然后重点对地震典型遗址、遗迹的综合评估原则进行了详细研究,并在此基础上设计出综合评估量表.最后,对北川、映秀等典型地震遗址、遗迹进行了综合评估,并提出了保护建议.     

关于陕西省城市防洪问题的思考

在系统总结陕西省城市改革发展的现状以及防洪减灾存在问题的基础上,指出了洪涝灾害造成的损失,重点说明城市防洪在经济建设中的重要性;针对省情提出了新时期城市防洪建设的思路、防洪策略和奋斗目标.山洪灾害是威胁中小城市安全的主要问题,要建立多元化的投资机制,鼓励和促进城市防洪建设健康发展.