不同酶强化污泥为燃料微生物燃料电池特性对比分析

采用单室无膜悬浮阴极微生物燃料电池(MFC),对比分析了蛋白酶和淀粉酶强化剩余污泥为燃料的MFC(ESMFC)产电特性、酶特性和污泥减量化效果。研究表明,投加蛋白酶的ESMFC最大功率密度比对照组增加106.2%,投加淀粉酶时ESMFC最大功率密度比对照组增加48%。蛋白酶作用主要体现在投加后的前12小时,而淀粉酶作用时间则较长,为投加后的前144小时,但在运行前期,由于高温作用,导致系统内的酶活性较强,投加的淀粉酶作用则不明显。投加蛋白酶的系统内TCOD、TSS和VSS去除率分别为82%、65%和85%,而投加淀粉酶的系统内TCOD、TSS和VSS去除率分别达到86%、67%和88%。此研究对于ESMFC中外加酶的选择具有一定意义。     

禾草灵对水稻生长和典型土壤酶活性的影响

禾草灵是一种广泛使用的除草剂，在土壤中大量残留，对非靶标生物产生危害。为探究除草剂对环境生物的毒性作用，本研究模拟水稻自然生长的环境，评估禾草灵对水稻及土壤微生物的影响。研究结果表明，低浓度禾草灵(200 μg L^-1)处理4 d对土壤微生物量没有显著影响(P>0.05)；8 d时，水稻生长没有明显变化，但土壤微生物量较对照组显著升高(P<0.05)。高浓度禾草灵(1 000 μg L^-1)处理4天后，土壤脲酶、酸性磷酸酶和过氧化氢酶的活性显著下降(P<0.05)，下降幅度分别为8.9%，16.6%和10.2%；处理8 d后，水稻幼苗鲜重显著降低(P>0.05)，叶绿素a和叶绿素b含量分别下降了13.5%和13.3%。本研究证实高浓度的禾草灵残留会对植物和土壤微生物产生不良的影响。     

基于主成分分析法的武汉城市圈区域协调发展研究

在"两型社会"背景下,如何实现武汉城市圈的快速发展及圈内的协调发展是促进武汉城市圈建设与发展的重要内容,也是构建中国中部区域板块新经济增长极的必然选择。采用统计数据、利用主成分分析法对武汉城市圈区域经济发展进行评价,利用数学模型对武汉城市圈区域发展的不平衡性与区域差异性进行分析,在此基础上提出发展地方特色经济,加强区域经济间的联系,实现产业一体化与经济一体化,建立统一的监督机构,实现武汉城市圈的协调发展。     

莱特生物强化技术处理高浓度有机废水的中试

采用莱特生物强化技术(LTBR—Littoral BioReactor),对兰州石化公司化工园区高浓度有机废水进行了中试试验,进行了正常运行的常规标定、水量冲击标定、浓度冲击标定。结果表明:采用LTBR生物处理工艺,使用特效微生物和营养基质,可以在高COD、高含盐等不利条件下正常进行有机物降解,达到了必须将废水中的COD降至2000mg/L以下的试验要求,为处理高浓度有机化工废水的工程应用开辟了新思路。     

Removal of arsenic from wastewater using iron compound: Comparing two different types of adsorbents in the context of LCA

A study was carried out in order to compare the environmental performance of two different types of adsorbents in removing arsenic (As) from wastewater. A FeCl₃-based adsorbent and a poly-Fe-based adsorbent were first synthesized and their abilities in adsorbing As from wastewater were investigated in terms of the adsorption density and the rate of adsorption. Here, it should be noted that the main material being used in the synthesis of the poly-Fe-based adsorbent was a waste product, known as polyferric sulfate or poly-Fe in short, which exits the manufacturing process of titanium dioxide.Both adsorbents were then compared in the context of life-cycle assessment (LCA). In other words, the experimental results (i.e. the value of the adsorption density and the rate of adsorption) were input into the LCA model in order to assess the environmental performance of each adsorbent in removing arsenic. An estimate for the environmental burden of each option was finally calculated as the sum of the depletion of abiotic resources (ADP), the global warming potential (GWP), the acidification potential (AP), the photo-oxidant formation potential (POCP), the eutrophication potential (EP), and the human toxicity potential (HTP). The main finding of this study was that the adsorption of arsenic by using the poly-Fe-based adsorbent is more attractive treatment option in the environmental protection point of view than the adsorption by using the FeCl₃-based adsorbent, which generates a relatively larger environmental burden.     

Effects of acute γ-irradiation on the aquatic microbial microcosm in comparison with chemicals

Effects of acute γ-irradiation were investigated in the aquatic microcosm consisting of green algae (Chlorella sp. and Scenedesmus sp.) and a blue–green alga (Tolypothrix sp.) as producers; an oligochaete (Aeolosoma hemprichi), rotifers (Lecane sp. and Philodina sp.) and a ciliate protozoan (Cyclidium glaucoma) as consumers; and more than four species of bacteria as decomposers. At 100 Gy, populations were not affected in any taxa. At 500–5000 Gy, one or three taxa died out and populations of two or three taxa decreased over time, while that of Tolypothrix sp. increased. This Tolypothrix sp. increase was likely an indirect effect due to interspecies interactions. The principal response curve analysis revealed that the main trend of the effects was a dose-dependent population decrease. For a better understanding of radiation risks in aquatic microbial communities, effect doses of γ-rays compared with copper, herbicides and detergents were evaluated using the radiochemoecological conceptual model and the effect index for microcosm.     

膜生物反应器中溶解性微生物产物特性的研究进展

溶解性微生物产物是制约生物处理出水达标和回用的主要污染物，处理工艺和操作条件的不同可能造成其特性差异。阐述了溶解性微生物产物的定义和产生机制，对膜生物反应器中溶解性微生物产物的组成、分子质量分布、亲水／疏水性、螯合性和毒性进行了概述，分析了影响其产生、特性和去除的因素。由于膜的截留作用使溶解性微生物产物在膜生物反应器中积累，容易引起膜污染。可以通过优化操作条件，减少溶解性微生物产物的产生，提高出水水质，有效地抑制膜污染。     

DGGE、T-RFLP 、LH-PCR对两种活性污泥的微生物种群多样性分析的比较

采用基于PCR扩增的分子生态技术DGGE、T-RFLP和LH-PCR，对2种典型污水处理系统中的活性污泥（生活污泥、焦化污泥）进行微生物种群多样性分析；并以此比较3种技术的优劣，提出不同应用条件下研究方法的选择依据。根据实验结果：DGGE得到的条带较多，但误差来源也最多；T-RFLP技术较为灵敏，但需要选择适当的内切酶，严格控制酶切条件，并且文库比对误差较大；而LH-PCR操作简单，结果稳定性较高。虽然目前尚无法判断3种方法的准确性，但LH-PCR在活性污泥的微生物种群多样性分析中已显示出潜在优势。     

微量金属元素及其配合物对厨余垃圾甲烷发酵的影响

生物可利用的微量金属元素不仅能够保证污染物以最大的速率转化，而且还可以使某些特殊的转化得以发生，并提高微生物对有毒污染物质的耐受能力。在研究厨余垃圾总固体浓度(total solid, TS)、接种量和C/N比对厨余垃圾厌氧发酵影响的基础上，重点探讨微量金属元素钴及其配合物丝氨酸对厨余垃圾厌氧发酵甲烷产量及关键酶含量的影响。结果表明，当TS为0.5%、接种污泥量为100 mL/L和C/N比为20∶1时，厨余垃圾厌氧发酵的甲烷产率较高，为367 mL/g COD；添加2 μmol/L的微量金属元素钴-配合物丝氨酸时，甲烷产率则提高到432 mL/g COD，相应地，辅酶M的含量由空白实验的41.21 μmol/g VSS提高到54.64 μmol/g VSS，辅酶F₄₂₀的含量由0.31 μmol/g VSS提高到0.48 μmol/g VSS。     

Leaching,mobility and persistence of tebufenozide in columns packed with forest litter and soil

Abstract

Leaching, downward mobility and persistence of tebufenozide was investigated under laboratory conditions in columns packed with forest litter and soil, after fortification with the analytical grade material (purity > 99.6%) and with two commercial formulations, RH‐5992 2F (aqueous flowable) and RH‐5992 ES (emulsion suspension). Two types of litter and soil were used: one type with relatively high amounts of sand and the other with high amounts of clay.

The concentrations eluted in the leachates were lower when the analytical material (dissolved in acetone) was used for fortification, than when the two formulations (diluted with water) were used. The amount leached was higher for RH‐5992 2F than for RH‐5992 ES. The type of substrate, i.e., sandy or clay type, had only marginal influence on the amounts eluted in the leachates. Downward movement of tebufenozide from the top 2‐cm layer to the untreated middle and bottom layers (3‐cm segments) was consistently lower when the analytical material was used for fortification, than when the two formulations were used. Downward movement was higher for RH‐5992 2F than for RH‐5992 ES. Persistence of tebufenozide in substrates, maintained under submerged conditions for 70 days after leaching, indicated an initial 2‐week lag period prior to the onset of degradation. Formulation‐related differences were observed in the half‐life (DT₅₀) values. When the analytical material was used for fortification, the DT₅₀ ranged from ca 54 to 59 d. However, when the formulations were used for fortification, the DT₅₀ showed a higher range, i.e., from ca 62 to 67 d for RH‐5992 2F and ca 70 to 80 d for RH‐5992 ES. Formulation ingredients appear to have caused enhanced adsorption of tebufenozide onto the substrates, thus delaying degradation.