Distribution characteristics of ammonia-oxidizing bacteria in the Typha latifolia constructed wetlands using fluorescent in situ hybridization(FISH)

A molecular biology method, fluorescent in situ hybridization（FISH）, in which the pre-treatment was improved in allusion to the media of the constructed wetlands（CW）, e.g. the soil and the grit, was used to investigate the vertical distribution characteristics of ammonia-oxidizing bacteria（AOB） quantity and the relation with oxidation-reduction potential（ORP） in the Typha latifolia constructed wetlands under three different Ioadings in summer from May to September. Results showed that the quantity of the AOB decreased in the Typha latifolia CW with the increase of vertical depth. However, the AOB quantity was 2-4 times the quantity of the control in the root area. Additionally, ORP in the rhizosphere was found to be higher than other areas, which showed that Typha latifolia CW was in an aerobic state in summer when using simulated non-point sewage at the rural area of Taihu Lake in China and small town combined sewage.     

稀土节能荧光灯生产过程中含汞废气处理的实践

用催化吸附 KMnO4溶液吸收化合净化法处理稀土荧光灯生产过程中含汞废气 ,经该工艺处理 ,排放的净化气低于GB162 97 1996《大气污染物综合排放标准》中汞污染物排放标准     

重金属阳离子荧光传感器合成及光谱性研究

通过亚胺缩合的反应制备出阳离子荧光传感器（Cation Fluorescent Sensors,CFSs）,并对其结构、光谱性能检测、荧光量子产率等进行了详细的研究.通过荧光化学传感器产生的荧光光谱一直是高效的分析方法,因此合成了新的基于席夫碱的荧光化学传感器,并研究了对各种金属离子的结合特性.在CH3CN溶液中测试了阳离子荧光传感器时不同阳离子的选择性响应,发现对Cu2＋有较好的选择性,可用于Cu2＋的检测.该类阳离子荧光传感器是基于2,2-联噻吩-5-乙醛的荧光发射基团和邻氨基苯甲醚为识别基团的一类阳离子荧光传感器.     

活性炭催化过氧化氢去除荧光增白剂

研究了活性炭(activated carbon,AC)吸附、改性活性炭(activated carbon modified,ACM)吸附、过氧化氢(H2O2)氧化、AC催化H2O2等方法对水体中荧光增白剂VBL的处理效果,并通过自由基俘获剂叔丁醇、催化过程气体分析等探讨了AC催化H2O2分解VBL的机制.结果表明,经硝酸铁[Fe(NO3)3]改性过的ACM对VBL的吸附去除率高于未改性的AC.活性炭催化H2O2对VBL的去除效果明显,但未改性AC催化去除率高于ACM.60 min时,AC催化氧化去除率即可达到95%以上,而ACM仅为58%.叔丁醇的加入降低了AC和ACM催化氧化对VBL的去除率,表明AC催化H2O2氧化能促进H2O2形成羟基自由基(·OH)和原子氧参与反应.AC催化H2O2分解及释放气体分析表明,AC能催化H2O2形成氧气并放热,且ACM明显快于AC.结合催化H2O2去除VBL效率的结果分析,ACM催化反应时活性中间物(自由基和原子氧等)产生速率快于AC,活性中间物自身消耗形成氧气,而不是用于分解VBL.催化反应中活性中间产物的形成速率与反应物供给速率的不匹配可能是导致ACM催化效果弱于AC的重要原因.     

基于代谢产物调控的活性污泥沉淀性能控制原理研究

通过对不同沉降性能活性污泥的胞外聚合物(EPS)进行荧光特性分析,探讨了荧光强度峰值、荧光区域积分等参数与污泥沉降性能的关系.研究表明,典型波长下荧光强度峰值与污泥沉降性能之间有很好关联性,据此,建立了微生物典型代谢产物与沉淀性能的调控曲线即活性污泥的安全操作线与微生物代谢状态曲线,确立了活性污泥沉淀性能调控区域即高代谢产物区可获得良好的固液分离效果.研究成果从微生物代谢的角度揭示了絮体结构的调控方法,具有重要的理论意义.     

上海市废旧荧光灯管回收体系建设的对策研究

废旧荧光灯管因含汞列入《国家危险废物名录》,若采取不当方式回收处置对环境存在污染隐患,由于多种原因大部分废旧荧光灯管未得到无害化处置,已经引起社会各界的关注和政府部门的重视。结合上海市的废旧荧光灯管产生及回收处置现状,针对法规、政策、机制方面存在的问题,通过研究提出源头控制、多渠道回收、建立豁免管理制度以及基金补贴机制等措施,为从根本上解决废旧灯管的回收难问题和探索社会源危险废物的管理提供了对策建议。     

废荧光灯的环境污染对策探讨

废荧光灯管中的有害物质如果处置不当,会对人体健康和环境造成危害。目前国内大部分废荧光灯管未得到无害化处置,主要在指定的法规、有效的政策以及完善的运营机制方面存在很多弊端,应引起社会各界的关注和政府部门的重视。本文结合国内外废荧光灯管回收处置现状,针对存在的问题,提出源头控制、分类收集、多渠道回收、建立资金及资金补贴机制以及技术手段措施,为从根本上解决废旧灯管回收难的问题,并探索社会源危险废物的管理提供对策建议。     

生活垃圾强制分类形势下的多源废荧光灯管回收管理机制建议

废荧光灯管的来源广泛,包括工业来源和社会来源,社会来源又包括居民来源,企业事业单位、公共场所等机构来源,具有多来源的特性。废荧光灯管中含有汞,若不经过妥善处理,会造成环境污染,对人的身体健康造成危害。随着国内生活垃圾分类的开展,废荧光灯管作为生活垃圾中有害垃圾的典型类别被强制分类,但仍存在很多问题。本文梳理了我国废荧光灯管的产生情况、LED灯替代情况,并对美国、欧盟、日本和我国国内典型城市的废荧光管理情况进行了总结。针对我国废荧光灯管的回收现状,从责任主体、责任划分、收集渠道、资金机制等角度提出了相关的管理建议,为推动我国废荧光灯管的管理提供借鉴。     

实时荧光定量PCR对A2/O短程硝化系统内氨氧化菌的定量分析

通过控制好氧区低DO浓度以及缩短好氧实际水力停留时间(actual hydraulic retention time,AHRT),在处理低C/N比实际生活污水的A2/O工艺中,成功启动并维持了短程硝化反硝化;系统亚硝酸盐积累率稳定维持在90%左右,氨氮去除率在95%以上。通过提取富集氨氧化菌(ammonia oxidizing bacteria,AOB)的基因组DNA,经两次常规PCR扩增和琼脂糖凝胶电泳,以纯化回收的DNA扩增片段作为实时荧光定量PCR检测AOB数量的DNA标准品,建立了检测AOB数量的实时荧光定量PCR标准曲线。利用实时荧光定量PCR技术比较了A2/O系统在不同运行条件及亚硝酸盐积累率情况下AOB菌群数量。结果表明,随着系统亚硝酸盐积累率的上升,系统内AOB菌群数量也大幅上升。全程硝化和短程硝化时,系统内的AOB菌群数量分别为5.28×109cells/g MLVSS和3.95×1010cells/g MLVSS。此外,亚硝酸盐积累率的下降相对于AOB菌群数量的下降有一定的滞后性。     

A method for the determination of rhodamine b and brilliant sulfaflavine on cotton string collectors and in a spray tank solution mixture

Abstract

A fluorescent method for the determination of rhodamine B (RhB) and brilliant sulfaflavine (BSF) dual tracers on cotton string collectors and in spray tank solutions was developed for the evaluation of the effects of adjuvants on the atmospheric drift of agricultural sprays. Both tracers on collectors were extracted with deionized water simultaneously and measured directly with a Fluorescent Specrometer by switching the maximum excitation and emission wavelengths. The linear ranges of the RhB and BSF standard curves were 0–50 and 0–10 ppb respectively. Recoveries of tracers on cotton strings ranged from 92.9% ± 1.1% to 95.1% ± 1.0% for RhB and 91.9% ± 2.8% to 103% ± 0.6% for BSF when spiked levels ranged from 0.25 to 2.5 μg per collector. The detection limit of the instrument was approximately 0.1 ppb for both tracers. The detection limits of the analytical method were approximately 0.1 ppb for RhB and 0.3 ppb for BSF when the background levels of cotton strings were subtracted. The presence of one tracer in the solution did not significantly interfere with the detection of the other tracer in the same solution. The presence of adjuvants added to the spray tank solutions did not interfere with the detection of both tracers when the adjuvants were applied at the manufacturer's maximum recommendation rates.