A new direct thermal desorption-GC/MS method: Organic speciation of ambient particulate matter collected in Golden, BC

Particulate matter having an aerodynamic diameter less than 2.5 μm (PM2.5) is thought to be implicated in a number of medical conditions, including cancer, rheumatoid arthritis, heart attack, and aging. However, very little chemical speciation data is available for the organic fraction of ambient aerosols. A new direct thermal desorption-gas chromatography/mass spectrometry (TD-GC/MS) method was developed for the analysis of the organic fraction of PM2.5. Samples were collected in Golden, British Columbia, over a 15-month period. n-Alkanes constituted 33–98% by mass of the organic compounds identified. PAHs accounted for 1–65% and biomarkers (hopanes and steranes) 1–8% of the organic mass. Annual mean concentrations were: n-alkanes (0.07–1.55 ng m⁻³), 16 PAHs (0.02–1.83 ng m⁻³), and biomarkers (0.02–0.18 ng m⁻³). Daily levels of these organics were 4.89–74.38 ng m⁻³, 0.27–100.24 ng m⁻³, 0.14–4.39 ng m⁻³, respectively. Ratios of organic carbon to elemental carbon (OC/EC) and trends over time were similar to those observed for PM2.5. There was no clear seasonal variation in the distribution of petroleum biomarkers, but elevated levels of other organic species were observed during the winter. Strong correlations between PAHs and EC, and between petroleum biomarkers and EC, suggest a common emission source – most likely motor vehicles and space heating.     

Non-conventional gas phase remediation of volatile halogenated compounds by dehydrated bacteria

Traditional biological removal processes are limited by the low solubility of halogenated compounds in aqueous media. A new technology appears very suitable for the remediation of these volatile organic compounds (VOCs). Solid/gas bio-catalysis applied in VOC remediation can transform halogenated compounds directly in the gas phase using dehydrated cells as a bio-catalyst.     

HPA／ZnFe2O4-TiO2光催化剂的制备及对马拉硫磷的可见光降解

以纳米TiO2载体,利用浸渍法制备了HPA／ZnFe2O4-TiO2光催化剂。对制备的催化剂进行了XRD、BET、TEM和UV-vis DRS表征。结果表明,催化剂样品均为锐钛矿相且ZnFe2O4很好地分散在载体表面,HPA／ZnFe2O4-TiO2光催化荆的平均粒径为10nm且在380-670nm均有强的光响应;反应最佳的HPA浓度为O.08molfL,最佳的ZnFe2O4负载量为1％。考察了HPA溶液初始浓度、ZnFe2O4负载量、溶液初始pH值、H2O2用量、催化剂用量对催化剂活性的影响。在溶液初始pH=13,H2O2=6mmol／L,催化剂用量为2g/L的最优条件下,光照反应进行100min后,马拉硫磷的降解率可达87％;重复4次后马拉硫磷的降解率仍可以达到67％。     

玄武湖挺水植物区与敞水区浮游甲壳动物昼夜水平迁移初探

浮游甲壳动物昼夜垂直迁移(DVM)是深水湖泊中的一种常见的现象,在浅水湖泊中,没有明显的下层滞水层为浮游甲壳动物提供避护所,浮游甲壳动物的垂直迁移活动不明显。但浅水湖泊挺水植物的存在为浮游甲壳动物提供了区别于敞水带的生境,结合理化、浮游植物和鱼的因素,对浅水湖泊玄武湖挺水植物区与敞水区浮游甲壳动物的昼夜水平迁移进行了研究。结果得出：浅水湖泊玄武湖中理化环境（如温度、溶解氧和pH)在荷花区、敞水区、荷花区与敞水区的交界区差异不大,对浮游甲壳动物的昼夜水平迁移不起主导作用。荷花区的浮游植物在质量和数量上低于敞水区,浮游甲壳动物在夜间捕食压力小的情况下会向敞水区移动。敞水区、交界区浮游甲壳动物在白天被捕食的风险要大于荷花区,因而白天时间浮游甲壳动物会迁移到荷花区聚集.     

论我国国际河流可持续开发利用的问题与法律对策

中国是世界上国际河流最多的国家之一,在国际河流的开发利用方面采取了一定的措施并取得了一定的成绩,但是在国际河流的可持续开发利用中仍存在不少问题,需要完善相关的国际与国内法律制度并采取其他有效的措施予以解决。从中国国际河流的概况出发,阐述对其进行可持续的开发利用在促进中国经济发展、加强民族团结以及保障国防安全等方面的重大意义,进而分析中国国际河流在可持续开发利用中存在的问题,包括立法缺失、保障措施缺位、管理机构缺乏等,最后从完善可持续开发利用的前提要素、确立可持续开发利用的基本原则、完善可持续开发利用的立法以及积极参与可持续开发利用的国际合作等方面提出解决上述问题的对策思考,以促进和保障我国国际河流可持续开发利用的实现.     

生态岛建设过程中环境类指标构建研究——以崇明岛为例

提出了将压力 状态 响应（PSR）模型与系统分析法理论集成起来构建生态岛建设过程中环境类指标的方法和步骤。指标构建过程分为4个步骤：（1）首先利用已有生态区域（岛）相关环境类指标确定备选指标集;（2）利用PSR模型对指标逻辑关系进行分析筛选;（3）以2010年为近期目标年,利用系统分析法确定指标核心要素,得到二次筛选指标;（4）以2030年为远期目标年,以综合性和动态性为依据确定最终指标。以上海市崇明岛为例,确定水、气、土为核心考核要素,构建了基于崇明生态岛建设过程的近期及远期目标的环境类考核指标体系。指标评价结果表明,崇明生态岛建设过程中环境类综合指数为72,其中环境压力指数、环境质量指数、环境保护指数分别为85、80和51,与崇明岛实际较为吻合。部分研究结果已在崇明岛生态建设过程中得到实际应用。     

Biosorption of nickel(II) from aqueous solution by Aspergillus niger: Response surface methodology and isotherm study

In the present study, the effects of biosorbent Aspergillus niger dosage, initial solution pH and initial Ni(II) concentration on the uptake of Ni(II) by NaOH pretreated biomass of A. niger from aqueous solution were investigated. Batch experiments were carried out in order to model and optimize the biosorption process. The influence of three parameters on the uptake of Ni(II) was described using a response surface methodology (RSM) as well as Langmuir and Freundlich isotherm models. Optimum Ni(II) uptake of 4.82 mg Ni(II) g⁻¹ biomass (70.30%) was achieved at pH 6.25, biomass dosage of 2.98 g L⁻¹ and initial Ni(II) concentration of 30.00 mg L⁻¹ Ni(II). Langmuir and Freundlich were able to describe the biosorption isotherm fairly well. However, prediction of Ni(II) biosorption using Langmuir and Freundlich isotherms was relatively poor in comparison with RSM approaches. The biosorption mechanism was also investigated by using Fourier transfer infrared (FT-IR) analysis of untreated, NaOH pretreated, and Ni(II) loaded A. niger biomass.     

Gas/particle partitioning of atmospheric PCDD/Fs in a satellite town in Eastern China

Gas/particle partitioning of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in ambient air was investigated in a satellite town in Eastern China from April 2007 to January 2008 comprehending large temperature variations (from 3 to 34 °C, daily average). Molecular weight, molecular structure and ambient temperatures are the three major factors that govern the gas/particle partitioning of atmospheric PCDD/Fs throughout the year. Generally, good agreements were obtained (except for winter) between measured particulate fractions and theoretical estimates of both the Junge–Pankow adsorption model and Harner Bidleman absorption model using different sets of subcooled liquid vapor pressure and octanol–air partition coefficient (K_oa), respectively. Models utilizing estimates, derived from gas chromatographic retention indices (GC-RIs), are more accurate than that of entropy-based. Moreover, during winter, the K_oa-based model using the GC-RIs approach performs better on lower chlorinated PCDD/Fs than that of -based. Furthermore, possible sources of mismatch between measured and predicted values in winter (3–7 °C) were discussed. Gas adsorption artifact was demonstrated to be of minor importance for the phenomena observed. On the other hand, large deviations of slopes (m_r) and intercepts (b_r) in logK_p vs. plots from theoretical values are observed in the literature data and these are found to be linearly correlated with ambient temperatures (P<0.001) in this study. This indicates that the non-equilibrium partitioning of PCDD/Fs in winter may be significantly influenced by the colder temperatures that may have slowed down the exchange between gaseous and particulate fractions.     

Degradation of pentachlorobiphenyl by a sequential treatment using Pd coated iron and an aerobic bacterium (H1)

The reductive dechlorination and biodegradation of 2,2^′4,5,5^′-pentachlorobiphenyl (PCB#101) was investigated in a laboratory-scale. Palladium coated iron (Pd/Fe) was used as a catalytic reductant for the chemical degradation of 2,2^′4,5,5^′-pentachlorobiphenyl, and an aerobic bacteria was used for biodegradation following the chemical reaction in this study. Dechlorination was affected by several factors such as Pd loading, initial soil pH and the amount of Pd/Fe used. The results showed that higher Pd loading, higher dosage of Pd/Fe and slightly acid condition were beneficial to the catalytic dechlorination of 2,2^′,4,5,5^′-pentachlorobiphenyl. In laboratory batch experiments, 2,2^′4,5,5^′-pentachlorobiphenyl was reduced in the presence of Pd/Fe bimetal, which was not further degraded by aerobic bacteria. 2,2^′,4-trichlorobiphenyl (PCB#17), a reduction product from 2,2^′4,5,5^′-pentachlorobiphenyl, was readily biodegraded in the presence of a aerobic bacterial strain. It is suggested that an integrated Pd/Fe catalytic reduction-aerobic biodegradation process may be a feasible option for treating PCB-contaminated soil.     

Polychlorinated dibenzo-p-dioxins, dibenzofurans and polychlorinated biphenyls levels in human breast milk from different regions of Turkey

Human breast milk offers the optimal nutrition for all infants and have been widely used in biomonitoring programs to assess human exposure to lipophylic environmental contaminants such as polychlorinated dibenzo-p-dioxins (PCDD), polychlorinated dibenzofurans (PCDF) and polychlorinated biphenyls (PCB). There are no previous reports from Turkey on chemically determined levels of PCDDs, PCDFs, and PCBs in human breast milk expressed as World Health Organization (WHO) toxic equivalents (TEQ). To get an overview of the levels of these contaminants in Turkish human milk, samples from 51 Turkish women living in the Ankara, İstanbul, Antalya, Kahramanmaraş, and Afyon provinces were analyzed by high resolution gas chromatography/high resolution mass spectrometry (HRGC/HRMS) throughout 2007. The mean concentrations of WHO_PCDD/F-TEQ and WHO_PCB-TEQ of all samples from the five regions were 7.5 and 3.1 pg g⁻¹ on a lipid basis, respectively. PCDD/F concentrations ranged between 0.78 and 29.3 pg WHO-TEQ g⁻¹ fat (1.7 and 36.2 pg WHO-TEQ g⁻¹ fat, respectively, including PCB). Of the five studied locations, the lowest levels of ∑TEQs (PCDD/F + PCB) were found in the Afyon (6.8 pg WHO-TEQ g⁻¹ fat) and the highest in the Antalya (15.6 pg WHO-TEQ g⁻¹ fat) province. The results have been discussed in terms of regions and PCDD/F and PCBs for which analyses had been made. The mean levels of PCDD/Fs and PCBs in Turkish human milk are comparable to that found in other countries.