λDNA体外重包装技术检测环境致突变物新方法及机理的研究

首次报道使用λＤＮＡ体外重包装技术检测化学物和环境污染致封变性取得了成功，辅以辅切和电泳技术，还可初步确定λＤＮＡ损伤的机遇。     

SBR法处理中药材有机废水工艺研究

应用ＳＢＲ法对中药材有机废水进行了研究。考察了ＣＯＤＣＲ、ＢＯＤ５、ＳＳ、ＮＨ３－Ｈ的处理效果，以及ＰＨ、水温、污泥负荷等条件对去除率的影响。运行结果表明，ＰＨＯ ６．０－９．０、ｔ为１５－３０℃、污沁荷０．３ｋｇＢＯＤ５／ｋｇＭＬＳＳ．ｄ，运行程序：进水０．５ｈ（限制曝气）、曝气１０ｈ、脱氮１．５ｈ，沉降０．５ｈ，排水０．５ｈ、闲置１１ｈ，周期时间２４ｈ时ＣＯＤＣＲ去除率８８％、ＢＯＤ５９４％、     

邻苯二甲酸酯类雌激素活性联合作用模型分析

环境雌激素对生命健康影响受到广泛关注,现行污染物环境标准制订和风险评价只针对单一化合物而非混合物效应,不足以保护生命安全与人类健康。为探讨环境雌激素的混合物效应,选择对雌激素敏感的人乳腺癌MCF-7细胞增殖实验,检测雌二醇(E2)、邻苯二甲酸酯类化合物(DBP和DEHP)的单一及其联合雌激素活性;基于单一化合物的浓度-反应曲线,运用浓度相加(CA)和独立作用(IA)模型对混合物的毒性进行预测,并将模型预测结果与混合物实验数据进行比较分析。结果表明,E2、DBP、DEHP对MCF-7细胞的单一作用数据可通过Weibull方程拟合,由拟合方程得到的半数效应浓度(EC50)及95%置信区间分别为3.450×10-6(2.373×10-6~1.675×10-5)、5.138(1.489~1.082×10)、1.186(4.478×10-1~2.24)μmol·L-1;3种化合物的混合物数据亦可通过Weibull、Logistic和Exp Gro1方程进行有效拟合,混合物效应与化合物单独作用产生的效应具有显著性差异;3种化合物表现非相似联合作用,利用独立作用(IA)模型预测混合物效应较为可靠,外源性环境雌激素与内源性雌激素联合作用产生的混合效应显著。环境雌激素混合物毒性可以通过相加作用模型预测,为环境复合污染的风险评价和管理提供基础数据。     

Competition for electrons between reductive dechlorination and denitrification

It is common that 2,4,6-trichlorophenol (TCP) coexists with nitrate or nitrite in industrial wastewaters. In this work, simultaneous reductive dechlorination of TCP and denitrification of nitrate or nitrite competed for electron donor, which led to their mutual inhibition. All inhibitions could be relieved to a certain degree by augmenting an organic electron donor, but the impact of the added electron donor was strongest for TCP. For simultaneous reduction of TCP together with nitrate, TCP’s removal rate value increased 75% and 150%, respectively, when added glucose was increased from 0.4 mmol?L^–1 to 0.5 mmol?L^–1 and to 0.76 mmol?L^–1. For comparison, the removal rate for nitrate increased by only 25% and 114% for the same added glucose. The relationship between their initial biodegradation rates versus their initial concentrations could be represented well with the Monod model, which quantified their half-maximum-rate concentration (K _S value), and K _S values for TCP, nitrate, and nitrite were larger with simultaneous reduction than independent reduction. The increases in K _S are further evidence that competition for the electron donor led to mutual inhibition. For bioremediation of wastewater containing TCP and oxidized nitrogen, both reduction reactions should proceed more rapidly if the oxidized nitrogen is nitrite instead of nitrate and if readily biodegradable electron acceptor is augmented.

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On the determination of nitrous oxide emission factor during biomass burning

ＯｎｔｈｅｄｅｔｅｒｍｉｎａｔｉｏｎｏｆｎｉｔｒｏｕｓｏｘｉｄｅｅｍｉｓｓｉｏｎｆａｃｔｏｒｄｕｒｉｎｇｂｉｏｍａｓｓｂｕｒｎｉｎｇＣａｏＭｅｉｑｉｕ；ＺｈｕａｎｇＹａｈｕｉ（ＲｅｓｅａｒｃｈＣｅｎｔｅｒｆｏｒＥｃｏ－ＥｎｖｉｒｏｎｍｅｎｔａｌＳｃｉ...     

氢氧化镁-壳聚糖复合絮凝剂对印染废水的脱色研究

使印染废水脱色是废水处理的重要问题,利用无枳／有机复合絮凝剂可取得优良的脱色效果。采用氢氧化镁一壳聚糖复合絮凝剂对印染废水进行脱色处理,研究了pH值、壳聚糖投加量、复合絮凝剂加入量等对脱色效果的影响。结果表明氢氧化镁一壳聚糖复合絮凝剂比单独使用氢氧化镁絮凝剂脱色效果好。壳聚糖是一种天然高分子化合物,是甲壳素的脱乙基产物。来源丰富,且具有无毒副作用、易降解等优点。利用壳聚糖作为复配剂制备的复合絮凝减少了镁盐的使用量,有效降低了废水处理成本,避免引起二次污染。     

论述造纸行业控制可吸附有机卤化物的必要性

造纸业漂白过程会带来可吸附有机卤化合物的污染,这是一类含有包括二恶英在内的多种有毒有机物。随着全球贸易进程,控制造纸业可吸附有机卤化合物的排放已经刻不容缓。控制造纸行业可吸附有机卤化物应从工艺技术、排放标准执行、监测等方面着手。     

一个基于专家知识的生态系统服务价值化方法

Costanza等提出的生态服务价值化评估方法在中国直接运用存在一些缺陷:低估或者忽略了某些生态系统服务价值。因此,笔者在其生态系统服务价值评估体系的基础上分别在2002年和2006年对中国700位具有生态学背景的专业人员进行问卷调查,得出了新的生态系统服务评估单价体系。通过对比发现,调查获得的基于专家知识的生态系统服务单价体系与基于物质量估算的生态系统服务价值之间具有较好的可比性。该基于专家知识的生态系统服务评估体系可以用于已知土地利用面积的生态系统服务价值估算,能在较短时间内获得较为精确的结果。     

从粉煤灰中提取多种微细氧化物的研究

将粉煤灰与Na2CO3按一定的比例混合后焙烧,采用酸碱联合法提取粉煤灰中氧化硅、氧化铝和氧化铁,分析了工艺条件对粉煤灰中氧化物提取率的影响。实验结果表明,从粉煤灰中提取氧化物的最佳条件是:碳酸钠与粉煤灰的比例0.6∶1.0,焙烧温度850℃、盐酸浓度4 mol/L,氢氧化钠浓度2.6 mol/L,浸取时间约6 h。在此条件下得出微细氧化硅、氧化铝、氧化铁的晶体,其平均粒度分别为氧化硅1.107μm,氧化铝1.334μm,氧化铁0.783μm。     

Catalytic destruction of pentachlorobenzene in simulated flue gas by a V2O5-WO3/TiO2 catalyst

Pentachlorobenzene (PeCB) in simulated flue gas was destructed by a commercial V₂O₅-WO₃/TiO₂ catalyst in this study. The effects of reaction temperature, oxygen concentration, space velocity and some co-existing pollutants on PeCB conversion were investigated. Furthermore, a possible mechanism for the oxidation of PeCB over the vanadium oxide on the catalysts was proposed. Results show that the increase of gas hourly space velocity (GHSV) and the decrease of operating temperature both resulted in the decrease of PeCB removal over the catalyst, while the effect of the oxygen content in the range of 5-20% (v/v) on PeCB conversion was negligible. PeCB decomposition could be obviously affected by the denitration reactions under the conditions because of the positive effect of NO but negative effect of NH₃. The introduction of SO₂ caused the catalyst poisoning, probably due to the sulfur-containing species formed and deposited on the catalyst surface. The PeCB molecules were first adsorbed on the catalyst surface, and then oxidized into the non-aromatic acyclic intermediates, low chlorinated aromatics and maleic anhydride.