染料厂污染土壤中六氯苯的水淹法厌氧降解

以乙酸为碳源,采用正交实验的方法,探讨了水淹法厌氧降解某染料厂污染土壤中六氯苯的效果,研究考察了初始pH、反应温度和固液比3个环境因素对六氯苯降解率的影响,确定了六氯苯最佳的厌氧降解条件。结果表明,初始pH对土壤中六氯苯的降解率影响最大。在初始pH为5,反应温度为45℃,固液比为1∶1的最佳反应条件下,六氯苯的降解率最高达到52.56%。     

一株耐铬不动杆菌对十二烷基硫酸钠的降解特性

研究醋酸钙不动杆菌H1的降解广谱性时,发现其能在高浓度十二烷基硫酸钠(SDS)环境中生长。经过对菌株H1降解特性研究,结果表明,该菌利用SDS的最适温度为30℃,最适pH为7.0,最适接种量为2%,并适应低渗透压环境。当SDS浓度低于400 mg/L时,菌株H1对SDS的降解率在85%以上,且在SDS浓度为400 mg/L时,达到最大降解率94%。当K2Cr2O7为500 mg/L时,菌株H1对SDS的降解率仍达到50%左右。添加酵母浸出物可促进SDS的降解。     

一株假单胞菌降解石油污染物的降解动力学与降解机制

从某石油污染场地土壤中分离出一株石油降解菌B-1(Pseudomonas),研究了该菌株降解石油污染物的动力学,通过气相色谱(GC)/质谱(MS)分析了石油组分降解前后的变化规律,并对其降解机制进行了初探。结果表明:(1)苯、二甲苯、萘的降解动力学拟合方程大部分与一级降解动力学方程拟合效果良好,苯、二甲苯、萘的降解半衰期分别为0.47~1.67、1.54~3.60、4.41~7.00d;(2)可以通过全扫描图谱及检索出的代谢产物明确微生物降解苯、二甲苯、萘的降解途径。     

突变灰盖鬼伞过氧化物酶降解刚果红的响应面法优化分析

酶法降解偶氮染料刚果红是一个复杂的过程,受温度、pH、酶量、刚果红浓度和双氧水浓度显著影响。为研究各因素及因素间交互作用对刚果红降解影响,提高刚果红的降解率,分别使用单因素法和响应面分析法对刚果红降解条件进行了优化。单因素实验结果显示灰盖鬼伞过氧化物酶降解刚果红的最适条件为：pH5．0、32℃、酶量4．98u、双氧水0．1mmol／L、刚果红20mg／L,此时刚果红最高降解率为34．84％。然后选双氧水浓度、刚果红浓度和灰盖鬼伞过氧化物酶量作为3个因素,通过中心组合设计实验,用响应面法对刚果红降解进行优化分析,最后得到一个拟合度良好的二次多项方程模型（R2=0．9900）。方差分析结果显示,刚果红浓度和酶量是影响最显著的因素,双氧水与酶以及染料与酶之间的交互作用极显著。响应面分析优化后的反应体系为：双氧水浓度0．15mmol／L,刚果红浓度为27．21mg／L,酶为2．07U,在此条件下,刚果红降解率达58．13％。     

铈离子光催化降解茜素绿的性能和机理

主要研究了简单铈离子（Ce3＋）在紫外光（uv）的作用下对蒽醌染料茜素绿（AG）的光催化降解效果和反应机理。结果表明,UV／Ce3＋体系能够有效降解AG,初始反应速率随AG浓度的倒数值和Ce3＋浓度的增加而线性增加,随初始溶液pH的增加先降低后增加,在酸性条件下有很高的TOC去除率。荧光探针实验表明,反应过程中可以产生·OH自由基。UV／Ce3＋体系对其他类型染料和对硝基苯酚都有较好的降解效果。     

降解SO_2功能菌的16S rRAN基因测序及降解特性

用低浓度SO2诱导驯化方法获得高效脱硫菌群,并用分离培养与16S rRNA基因测序技术相结合的方法鉴定菌群种属,分析驯化过程中种群结构的动态变化,同时研究分离纯菌种的脱硫性能。结果表明,从诱导驯化7 d和14 d菌液中分别分离出23株菌和22株菌,16S rRNA序列分析发现这些菌归属于13个种,其中有6个种（Rhodococcus erythropolis、Pseudomonas putida、Microbacterium oxydans、Sphingomonas koreensis、Acinetobacter junii、Acinetobacter johnsonii）对SO2-3有较强的降解能力,并在持续驯化过程中稳定的生长传代,降解产物以硫酸根为主,还有极少量的单质硫。与含混合菌的驯化菌液降解SO2-3的能力相比,单一脱硫菌的脱硫性能较弱。脱硫功能菌株及其基本特性的研究为微生物处理SO2烟气提供了丰富的菌源信息和理论基础。     

采油废水厌氧处理系统的微生物群落特征

为了深入认识石油烃的厌氧降解过程,利用分子生物学技术分析了大庆油田采油废水处理系统厌氧池和进水中的微生物群落特征。基于DGGE和克隆文库的分析结果均表明,厌氧生物膜中存在的古菌源自于采油废水。厌氧生物膜和采油废水中的古菌主要是产甲烷菌,包括嗜甲基的Methanomethylovorans thermophila和利用氢和甲酸的Methanolinea tarda。值得注意的是,氢营养型的M.tarda在厌氧生物膜中得到了富集。进水和厌氧生物膜中的细菌群落结构明显不同。进水中的主要细菌类群为Epsilonproteobacteria,而生物膜中的主要类群为Nitrospira和Deltaproteobacteria。在厌氧生物膜中发现许多与产甲烷古菌(尤其是氢营养型产甲烷菌)协同降解石油烃类物质的细菌相关克隆:其中一个克隆与Syntrophus具有较高的同源性,该类菌是产甲烷菌介导的厌氧烃降解微生物区系中的关键细菌;许多Deltaproteobacteria克隆属于group TA类群,该类群细菌主要参与芳香族化合物产甲烷菌介导的厌氧降解过程。这些结果表明,在大庆油田采油废水厌氧处理系统中已经建立起由产甲烷菌所介导的厌氧石油烃降解的微生物区系。     

不同处理技术对河流污染物降解系数影响的比较

以苏州官渎花园内河为研究背景,利用模拟河道分别考察了曝气复氧、人工水力循环、渗滤净化技术3种处理技术对受污河水中COD降解系数k COD、NH3-N降解系数k NH3-N变化规律的影响。实验表明,在无外源污染且河水滞留的天然情况下河道拥有一定自我净化的能力,并且3种处理技术对COD、NH3-N的降解系数都有一定提高,分别使k COD增加了34.3%、47.8%和57.8%,k NH3-N增加了8.35%、15.4%和52.8%,结果显示,渗滤净化技术对污染物降解系数的提高影响最大。     

The selective role of nitrite in the PAO/GAO competition

Proliferation of Glycogen Accumulating Organisms (GAOs) accounts as one of the major bottlenecks in biological phosphorus removal systems. GAO outcompeting polyphosphate accumulating organisms (PAOs) results in lower P-removal. Thus, finding optimal conditions that favour PAO in front of GAO is a current focus of research. This work shows how nitrite can provide a novel strategy for PAO enrichment. A propionate-fed GAO-enriched biomass (70% Defluviicoccus I, 18% Defluviicoccus II and 10% PAO) was subjected more than 50 d under anaerobic-anoxic conditions with nitrite as electron acceptor. These operational conditions led to a PAO-enriched sludge (85%) where GAO were washed out of the system (<10%), demonstrating the validity of the new approach for PAO enrichment. In addition, the presented suppression of Defluviicocus GAO with nitrite represents an add-on benefit to the nitrite-based systems since the proliferation of non-desirable GAO can be easily ruled out and added to the other benefits (i.e. lower aeration and COD requirements).     

Degradation of atrazine using solar driven fenton-like advanced oxidation processes

Atrazine (2-chloro-4-ethylamino-6-isopropylamino-s-triazine) was degraded using cobalt-peroximonosulfate (Co/PMS) advanced oxidation process (AOP). Three Co concentrations (0.00, 0.25 and 0.50 mM) and five peroximonosulfate (PMS) concentrations (0, 5, 8, 16 and 32 mM) were tested. Maximum degradation reached was 88% using dark Co/PMS in 126 minutes when 0.25 mM of cobalt and 32 mM of PMS were used. Complete atrazine degradation was achieved when the samples were irradiated by the sun under the same experimental conditions described. Tests for identification of intermediate products allowed identification and quantification of deethylatrazine in both dark and radiated conditions. Kinetic data for both processes was calculated fitting a pseudo-first order reaction rate approach to the experimental data. Having kinetic parameters enabled comparison between both conditions. It was found that the kinetic approach describes data behavior appropriately (R² ≥ 0.95). Pseudo-kinetic constants determined for both Co/PMS processes, show k value of 10^?4 for Co/PMS and a k value of 10^?3 for Co/PMS/ultraviolet (UV). This means, that, with the same Co/PMS concentrations, UV light increases the reaction rate by around one order of magnitude than performing the reaction under dark conditions.