The estimation of bioconcentration factors of aromatic hydrocarbons by high‐performance liquid chromatography

The determination of Bioconcentration Factors (BCF) via HPLC capacity factors (k') has been studied, including the effect of column type and mobile phase composition on the correlation between log BCF and log k’. Values of BCF correlate well with the phenylsilica column capacity factors. The phenylsilica column followed by C18 column give better correlations than either C8 or C2 column. The use of HPLC with phenylsilica as stationary phase and methanol‐water as mobile phase in the prediction of BCF can be at least as good or better than the use of n‐octanol/water partitioning system. There are no significant differences in the correlations between log k’ and log BCF with the changes of methanol concentration in the mobile phase, and it seems that a high proportion of methanol in the eluent is required to obtain good results.     

Mercury pollution in a mining area of Guizhou,China: Fluxes over contaminated surfaces and concentrations in air,biological and geological samples

A dynamic flux chamber has been used to estimate fluxes of mercury over different types of surfaces in an abandoned open‐cut mine of Tongren prefecture, Guizhou province, China during spring and summer of 1996. The highest fluxes were obtained over cinnabar slag and contaminated soils, whereas the emissions above cinnabar ore were substantially lower. These fluxes was scaled up to estimate the contribution of mercury emissions to air from mercury wastes, compared to anthropogenic activities in the province of Guizhou, China. Atmospheric mercury concentrations measured were enhanced in the mining area (<1.3 μg m^‐3) compared to regional background sites (1.8–5.1 ng m^‐3). The spreading of mercury was estimated by using biological and geological samples. Moss bags have been employed to estimate long‐time dry‐ and wet‐deposition to this area.     

Determination and QSPR analysis of log Kow and log Koc for fluorine containing benzene derivatives

Octanol‐water partition coefficients (Kow) and soil organic carbon sorption coefficients (Koc) were determined for 14 fluorinated benzene derivatives. Quantitative structure‐property relationships were developed using molecular connectivity indices and quantum chemical parameters to analyze the most significant factors influencing these physico‐chemical properties of the compounds. The substitution by F in benzene derivatives has greater influence on Koc than on Kow.     

利用甘油脱水酶基因构建产3-羟基丙醛工程菌及其表达比较

3-羟基丙醛(3-HPA)是一种重要的化工产品,可由甘油经甘油脱水酶作用后生成.为获得产3-HPA基因工程菌,在已构建含甘油脱水酶基因及其激活因子大亚基质粒pEtac-dhaB-gdrA的基础上,构建了包含小亚基gdrB激活因子的重组质粒pEtac-dhaB-gdrA-gdrB.利用大肠杆菌通用tac启动子将该质粒在不同Escherichia coli BL21、DH5a及JM109中进行表达.阳性转化子经IPTG诱导后,提取总RNA,以cDNA为模板进行RT-PCR发现,目标基因在不同宿主都能较好转录.SDS-PAGE、酶活测定和3-HPA浓度测定结果表明,目标蛋白表达存在差异;酶活分别为4.7(±0.44)、3.5(±0.95)、8.1(±0.66)U/mg;发酵液中3-HPA的含量分别为0.012(±0.0044)、0.014(±0.003)、0.375(±0.018)g L-1,重组E.coli JM109/pEtac-dhaB-gdrA-gdrB具有较好的甘油脱水酶基因表达和产3-HPA性能.该基因工程菌与克雷伯氏菌(Klebsiella pneumoniae)相比,发酵副产物明显较少,有利于后期提取,为生产3-HPA提供了一条新思路.     

The abatement of major pollutants in air and water by environmental catalysis

This review reports the research progress in the abatement of major pollutants in air and water by environmental catalysis. For air pollution control, the selective catalytic reduction of NO _x (SCR) by ammonia and hydrocarbons on metal oxide and zeolite catalysts are reviewed and discussed, as is the removal of Hg from flue gas by catalysis. The oxidation of Volatile organic compounds (VOCs) by photo- and thermal-catalysis for indoor air quality improvement is reviewed. For wastewater treatment, the catalytic elimination of inorganic and organic pollutants in wastewater is presented. In addition, the mechanism for the procedure of abatement of air and water pollutants by catalysis is discussed in this review. Finally, a research orientation on environment catalysis for the treatment of air pollutants and wastewater is proposed.     

中国汞污染的来源、成因及控制技术路径分析

汞是一种能长期存在于环境且具有全球迁移性的污染物.汞污染防治是一个复杂的系统工程,涉及多部门、多领域、多行业,国家需要在政策、管理和技术等方面采取综合的战略措施推进汞污染防治.本文基于汞污染的环境和社会影响,分析了中国汞污染的来源、成因并评估了中国汞管理体系,结合中国参加全球汞公约谈判的特定背景,识别出汞污染防控的优先行业,包括汞的无意排放优先控制行业:燃煤、有色金属冶炼、汞矿开采和含汞废物处理;汞的有意使用优先控制行业:电石法聚氯乙烯生产,医疗产品、荧光灯和电池生产.本文也进一步提出了汞污染控制技术路径,包括构建汞风险管理和识别平台、完善汞管理体系、加强环境技术研发、推进绿色转型、保护环境和公众健康等.     

东湖、汤逊湖和梁子湖沉积物磷形态及pH对磷释放的影响

文章采用淡水沉积物中磷形态标准测试程序(SMT)研究了东湖、汤逊湖和梁子湖沉积物中磷的形态分布,并比较了不同pH条件下沉积物磷释放特征的差异性。结果表明:东湖沉积物总磷质量分数最高,平均值1.232 mg.g-1,其次为汤逊湖(0.762mg.g-1),梁子湖沉积物总磷质量分数最低(0.572 mg.g-1);3个湖泊上覆水总磷质量浓度也表现出类似的变化规律,线性相关性分析显示上覆水中总磷质量浓度与沉积物总磷质量分数显著正相关。东湖和梁子湖沉积物总磷中无机磷和有机磷所占比例较接近,汤逊湖无机磷所占比例远低于有机磷。不同湖泊之间磷形态的分布并没有一定的规律性,湖泊的地理分布以及人为因素可能是造成磷形态差异的主要因素。当pH为2.0~7.0时,3个湖泊沉积物中溶解性活性磷(SRP)释放量均呈先增加后减小的趋势;当pH为7.0~12.0时,SRP释放量呈增加趋势。相关分析结果表明,SRP的释放与有机质的质量分数无显著相关性。方差分析结果显示3个湖泊沉积物在黏粒和粉粒组成上均没有显著差异(P>0.1),表明实验样品的粒径组成不是造成各个湖泊间磷释放差异的原因。不同pH条件下,SRP释放量与沉积物总磷质量分数显著正相关;酸性环境下,SRP释放量与酸式磷(HCl-P)的相关性优于碱式磷(NaOH-P),碱性环境下则刚好相反。     

离子液体分析方法研究进展

离子液体(ILs)由于挥发性小和化学稳定性高常称为绿色溶剂而得以广泛生产与应用.同时由于水溶性高和难降解可能给水生生物带来潜在危害,已逐渐引起广大环境化学工作者的关注.如何有效地分离分析ILs是研究其迁移、转化等环境行为及生物毒性的首要问题.为此,本文系统论述了反相液相色谱法、离子对-反相液相色谱法、极性-反相液相色谱法、离子色谱法、毛细管电泳及等速电泳等方法分析ILs的研究进展,分析了各个方法的优缺点和适用对象,展望了ILs分离分析发展的未来趋势.     

模拟日光照射下三种抗生素的光降解行为

选取四环素、土霉素、红霉素等3种国内普遍使用的抗生素,研究其在模拟日光(1.7 kW氙灯,300 nm≤λ≤400 nm)下的降解动力学行为.结果表明,3种抗生素在模拟日光下均能发生光降解,3 h的降解率分别达到66.87%、90.55%和92.80%.降解过程均符合准一级反应动力学方程,速率常数(k)分别为:0.0064、0.0138 min-1和0.0155 min-1;半衰期(t1/2)分别为:108.30、50.23、44.72 min.采用LC-MS分析推断3种抗生素主要降解产物,探讨了它们可能的光解途径.