不同地域人发中重金属污染特征与来源解析

以某高校新生发样为研究样本,将生源地分为东北、西北、西南、华北、华南、华中、华东7个地域,采用电感耦合等离子发射光谱法对发样中所含铬、铜、镍、铅、锌进行测定,通过非参数检验及偏相关性检验分析不同地区发样中重金属含量与性别、身体质量指数(BMI)的关系。结果显示,所采集发样中铬、铜、镍、铅、锌的含量变化范围依次为0.22~101.84、0.36~112.24、0.70~128.75、1.39~136.13、1.12~719.50μg/g;发样中重金属浓度的地区排序为东北>华东>华北>西北>华中>西南>华南。聚类分析和主成分分析结果显示,不同地区发样中重金属的来源有所差异:东北、西北、华北地区发样中重金属可能主要来源于燃煤、工业生产过程、机动车排放,方差贡献率分别为39.47%、25.78%、22.89%;华中、华东、西南、华南地区发样中重金属可能主要来源于工业生产过程、机动车排放、冶金化工过程,贡献率分别为47.76%、27.51%、18.24%。相关性检验显示,男性发样内铬、铜、镍、铅含量高于女性。其中,偏胖或偏瘦女性存在较高的铅暴露风险;40.2%的男性发锌含量低于正常值下限,24.4%的女性发锌含量低于正常值下限,且偏瘦女性发内缺锌现象显著;男、女发铜含量高于正常值上限的比例分别为91.8%、85.6%,存在不同程度的铜暴露风险。     

顶空固相微萃取-气相色谱法测定水中四乙基铅

建立了水中四乙基铅的测定方法——顶空固相微萃取-气相色谱法,探讨了影响水中四乙基铅萃取效率的温度、转速和萃取时间等因素。实验结果表明,在0.08～10μg/L范围内线性关系良好,方法检出限为0.02μg/L,实际水样加标回收率为96.2%～98.3%。     

高效液相色谱-氢化物发生-原子荧光光谱联用技术测定水中烷基汞

建立了高效液相色谱(HPLC)-氢化物发生(HG)-原子荧光光谱(AFS)联用技术分析地表水及废水中甲基汞和乙基汞的方法。样品经二氯甲烷萃取,再以半胱氨酸+乙酸铵溶液反萃取富集,并进入高效液相色谱分离,经形态分析预处理装置后,借助原子荧光光谱法检测。在优化分离条件下,甲基汞和乙基汞在1～50μg/L范围内呈现良好的线性关系,对于标准水样、地表水和废水实际水样,加标平均回收率均为80%～110%。平行进样7次1μg/L的汞混合标准溶液,甲基汞和乙基汞的色谱峰面积的相对标准偏差分别为5.2%和3.9%,检出限则分别为0.4 ng/L和0.7 ng/L。该检测方法前处理简单、回收率稳定、灵敏度和准确度高、检出限低、杂质干扰少、监测费用低,便于在普通实验室推广和应用。     

支撑排污许可制度的固定源监测技术体系完善研究

排污许可制度是固定源核心管理制度,对污染源监测技术提出"便捷、智能、精细"的发展要求,依规发证、依证管理2个阶段均需要污染源监测技术的有效支撑.针对当前污染源监测技术体系现状,应进一步完善自行监测技术指南体系,对发证行业指南实施情况跟踪评估,适时修订;为将工业园区纳入核发排污许可证范围扎牢基础,制定工业园区自行监测技术...     

铅蓄电池企业废气中铅及其化合物便携式XRF检测方法

在企业污染源现场实现污染物排放浓度水平的快速判定和超标风险筛查,对生态环境管理部门提高执法效率、企业提高环境管理水平意义重大。铅是一种对人体危害极大的有毒重金属,目前缺少含铅废气中铅及其化合物的便携式直读检测设备和检测方法。探索性地将X射线荧光光谱(XRF)法应用于铅蓄电池企业含铅废气中铅及其化合物的便携式快速、直读检测。研究结果表明,基于XRF的面密度法适用于铅蓄电池企业含铅废气处理设施后铅及其化合物的快速、直读检测,相对国标方法具有快速、直读、对样品无损、便于复测等特点,可用于铅及其化合物排放浓度水平的快速判定和超标风险筛查。     

Characterization of depth-related microbial communities in lake sediment by denaturing gradient gel electrophoresis of amplified 16S rRNA fragments

The characterization of microbial communities of different depth sediment samples was examined by a culture-independent method and compared with physicochemical parameters, those are organic matter （OM）, total nitrogen （TN）, total phosphorus （TP）, pH and redox potential （Eh）. Total genomic DNA was extracted from samples derived from different depths. After they were amplified with the GC-341 f/907r primer sets of partial bacterial 16S rRNA genes, the products were separated by denaturing gradient gel electrophoresis （DGGE）. The profile of DGGE fingerprints of different depth sediment samples revealed that the community structure remained relatively stable along the entire 45 cm sediment core, however, principal-component analysis of DGGE patterns revealed that at greater sediment depths, successional shifts in community structure were evident. The principle coordinates analysis suggested that the bacterial communities along the sediment core could be separated into two groups, which were located 0-20 cm and 21-45 cm, respectively. The sequencing dominant bands demonstrated that the major phylogenetic groups identified by DGGE belonged to Bacillus, Bacterium, Brevibacillus, Exiguobacterium, γ-Proteobacterium, Acinetobacter sp. and some uncultured or unidentified bacteria. The results indicated the existence of highly diverse bacterial community in the lake sediment core.     

Enhanced adsorption of hexavalent chromium by a biochar derived from ramie biomass (<Emphasis Type="Italic">Boehmeria nivea</Emphasis> (L.) Gaud.) modified with β-cyclodextrin/poly(L-glutamic acid)

This paper explored biochar modification to enhance biochar’s ability to adsorb hexavalent chromium from aqueous solution. The ramie stem biomass was pyrolyzed and then treated by β-cyclodextrin/poly(L-glutamic acid) which contained plentiful functional groups. The pristine and modified biochar were characterized by FTIR, X-ray photoelectron spectroscopy, specific surface area, and zeta potential measurement. Results indicated that the β-cyclodextrin/poly(L-glutamic acid) was successfully bound to the biochar surface. Batch experiments were conducted to investigate the kinetics, isotherm, thermodynamics, and adsorption/desorption of Cr(VI). Adsorption capacities of CGA-biochar were significantly higher than that of the untreated biochar, and its maximum adsorption capacity could reach up to 197.21 mg/g at pH 2.0. Results also illustrated that sorption performance depended on initial solution pH; in addition, acidic condition was beneficial to the Cr(VI) uptake. Furthermore, the Cr(VI) uptake was significantly affected by the ion strength and cation species. This study demonstrated that CGA-biochar could be a potential adsorbent for Cr(VI) pollution control.     

珠穆朗玛峰地区近200年冰芯草酸根记录及其环境意义

 1997年5月中美联合珠峰地区绒布冰川考察期间，在远东绒布冰川海拔6500m北支冰流粒雪盆内钻取到一支41m长冰芯.该冰芯定年至1814年．远东绒布冰芯中近200年来草酸根浓度变化与Ca²⁺和NH₄浓度变化一致性较差，表明草酸根的来源有别于大气尘埃和生物来源．草酸根浓度与冰芯中气温指标δ¹⁸O的变化具有一致性,说明气温是影响大气中草酸根浓度变化的因素之一，但非主导因素.远东绒布冰芯记录的20世纪以来草酸根浓度的迅速升高反映了人类工业活动对大气环境的污染．20世纪50～80年代，大气中受人类工业活动污染的草酸根浓度约为19世纪自然本底值的3倍，其中60年代人类活动排放的草酸盐类对大气的污染最为严重.     

高温油品泄漏图象特性的实验研究

通过对不同性质的高温油品发生泄漏时图象特性的分析,工出泄漏油品蒸汽浓度与图象灰度之间的关系。在此基础上通过图象处理技术来判别出现的物质是否为泄漏油品,从而实现高温油品泄漏火灾的早期报警。