藏南干旱区湖泊及地热水体氢氧同位素研究

青藏高原水循环过程情况复杂,水体氢氧同位素包含了其重要信息.选取西藏南部干旱区淡水湖、咸水湖及地热水水体为研究对象,分析研究区内不同水体氢氧同位素组成、变化特征、影响因素及水循环过程.结果表明,3种水体均表现出了高海拔地区氢氧同位素组成偏负的特点,淡水湖打加芒错δ18O平均值为-17.0‰,δD平均值为-138.6‰,咸水湖朗错δ18O平均值为-6.4‰,δD平均值为-87.4‰,搭格架地热区热水δ18O平均值为-19.2‰,δD平均值为-158.2‰;受内陆干旱区强烈的蒸发作用影响,湖泊及地热水蒸发线斜率均小于8,氘过量d值均为负值;搭格架地热区热储温度较高,氢氧同位素关系存在氧漂移现象.     

典型再生水人工湿地净化系统水质时空变异研究——以北京市奥林匹克森林公园人工湿地为例

选取奥林匹克森林公园人工湿地作为典型再生水补水人工湿地净化系统进行水质数据检测,应用模糊综合评价法综合评估各净化单元的水体污染状况,采用综合判别分析和Spearman相关分析阐释影响各净化单元时空变异的水环境要素,并通过因子分析识别不同时间段污染源的种类和组成.结果表明,奥林匹克森林公园人工湿地净化系统水质状况较好,符合人体非直接接触的景观用水国家标准.人工湿地各净化单元时空区间污染程度不同:季节尺度上,秋季污染更为严重;空间尺度上,主湖区、混合氧化塘区污染最为严重.CODMn、NO-3-N、ORP、TN 4项指标即可完全表征水质的季节差异(91.8%),应适当加大监测力度;Chl-a、CODMn、DO、pH 4项指标用于表征空间差异(55.1%),较低的判别正确率暗示了各功能区间类似的污染状况.不同时空区间污染源种类和组成存在差异性:水体的内源杂质是各季度影响水质的主要因子,春季有机污染最为严重,夏季则转为氮、磷等营养物质污染,秋季水体则更易受富营养化的威胁;再生水区水体污染的主要影响因子为氮、磷等营养盐类,其余功能区水体主要影响因子仍为内源杂质.增强水体流通力,缩短水力停留时间,能够有效减弱富营养盐类和有机污染物的影响.     

焦化行业SO2排放现状及减排潜力分析

随着钢铁工业的高速发展,高温炼焦已成为中国煤炭资源利用的重要途径之一,与此同时焦化行业SO2排放污染问题越来越引起人们的关注.2007年,全国焦炭产量总计335.53 Mt,其中机械化焦炉产量达305.37 Mt,约占全国焦炭产量的91.01%,焦化行业SO2排放量达181.19 kt.在参考国家制定的焦化行业未来产业...     

基于景观格局演变的流域生态风险评价与管控——以贵州赤水河流域为例

以岩溶地区典型流域——赤水河流域为研究对象,以2000、2005、2008、2013年4期遥感数据为基础,结合Arc Map的空间分析功能,对流域景观格局演变过程进行分析,构建流域生态风险评价体系与管控措施。研究表明:2000~2013年赤水河流域无风险区、潜在风险区、轻度风险区分别由1.66、2.95、75.41 km~2上升至5.63、21.81、115.45 km~2,而中度、重度风险区却分别下降了35.6和40.27 km~2;历年生态风险演变格局为以城乡建设用地为中心,生态风险由轻度、中度、重度向潜在或无风险区过渡,轻度、中度、重度主要以点状扩散或增加,潜在及无风险区则连片分布于农田区和山地丘陵区;基于不同生态风险区的风险源管控对策,对建立流域生态风险预警机制、降低流域生态环境风险、维护流域生态服务功能具有十分重要的意义。     

利用中巴地球资源卫星数据反演武汉市湖泊营养状态指数

以武汉市主要湖泊为例，研究了利用中巴地球资源卫星（CBERS2）数据反演水体营养状态指数（TLI）。研究旨在评估利用中巴地球资源卫星数据来估算内陆水体富营养化程度的可能性。首先利用地面水质监测数据计算武汉市某些湖泊监测点的“真实的”营养状态指数（包括综合营养状态指数和修正的Carlson营养状态指数），同时，在事先经过辐射校正和几何校正的CBERS2图像上，以9×9像元为采样窗口，提取各个对应地点的灰度值均值（从波段1至波段4）；然后，采用多元逐步回归分析，以各波段灰度值均值为自变量，建立营养状态指数经验遥感反演模型；最后，利用模型对整个湖泊水体的营养化状态指数进行反演，并绘制了其空间分布图。 结果显示，营养状态指数的自然对数值与CBERS2图像各波段灰度值之间存在较好相关关系，回归系数平方值(R²)为0.51。利用反演模型反演得到的湖区水质分布与实际情况基本相符。由于CBERS2图像数据可以从我国许多数据分发中心免费获取，这为低成本的水质遥感监测提供了一条途径。     

Measurement of Volatile Organics at Part per Billion Concentrations Using a Cold Trap Inlet and High Speed Gas Chromatography

Direct inlet gas chromatography (GC) is becoming one of the most frequently used techniques for measurement of volatile organics in air. Although GC is an effective tool, its usefulness as a field method can be limited by retention times of several minutes or more, and by the limits of detection. In order to address these issues, a high speed GC system featuring a capillary cold trap inlet and variable speed electrometeramplifier was developed and tested.

The gas cooled inlet was used to collect and focus organic vapors from injection volumes of up to 1 ml. Resistance heating of the metal cold trap produced a narrow injection band that allowed simple separations to be completed in 5 to 20 seconds. Use of a variable speed electrometer-amplifier allowed the response time and noise suppression characteristics to be adjusted to the needs of the specific analysis.

Simple mixtures of organics including aromatics, alkanes and chlorinated hydrocarbons were separated in 20 seconds or less. The limits of detection for 13 test compounds ranged from less than 1 part per billion by volume (ppbv) to about 50 ppbv. Data presented here indicate that high speed GC using a cold trap inlet may be a feasible approach for near real-time measurement of volatile organics in ambient air.     

Estimation and characterization of unintentionally produced persistent organic pollutant emission from converter steelmaking processes

Unintentionally produced persistent organic pollutants (UP-POPs) including polychlorinated dibenzo-p-dioxins, and dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs), and polychlorinated naphthalenes (PCNs) were characterized and quantified in stack gas and fly ash from the second ventilation systems in five typical converters in five different steelmaking plants. The 2378-substituted PCDD/Fs (2378-PCDD/Fs) and dioxin-like PCB (dl-PCBs) toxic equivalents (TEQs) were 1.84–10.3 pg WHO-TEQ Nm^?3 in the stack gas and 5.59–87.6 pg WHO-TEQ g^?1 in the fly ash, and the PCN TEQs were 0.06–0.56 pg TEQ Nm^?3 in the stack gas and 0.03–0.08 pg TEQ g^?1 in the fly ash. The concentrations of UP-POPs in the present study were generally lower than those in other metallurgical processes, such as electric arc furnaces, iron ore sintering, and secondary metallurgical processes. Adding scrap metal might increase UP-POP emissions, indicating that raw material composition was a key influence on emissions. HxCDF, HpCDF, OCDF, HpCDD, and OCDD were the dominant PCDD/Fs in the stack gas and fly ash. TeCB and PeCB were dominant in the stack gas, but HxCB provided more to the total PCB concentrations in the fly ash. The lower chlorinated PCNs were dominant in all of the samples. The 2378-PCDD/F, dl-PCB, and PCN emission factors in stack gases from the steelmaking converter processes (per ton of steel produced) were 1.88–2.89, 0.14–0.76_, and 229–759 μg t^?1, respectively.     

Aging and compressibility of municipal solid wastes

The expansion of a municipal solid waste (MSW) landfill requires the ability to predict settlement behavior of the existing landfill. The practice of using a single compressibility value when performing a settlement analysis may lead to inaccurate predictions. This paper gives consideration to changes in the mechanical compressibility of MSW as a function of the fill age of MSW as well as the embedding depth of MSW. Borehole samples representative of various fill ages were obtained from five boreholes drilled to the bottom of the Qizhishan landfill in Suzhou, China. Thirty-one borehole samples were used to perform confined compression tests. Waste composition and volume-mass properties (i.e., unit weight, void ratio, and water content) were measured on all the samples. The test results showed that the compressible components of the MSW (i.e., organics, plastics, paper, wood and textiles) decreased with an increase in the fill age. The in situ void ratio of the MSW was shown to decrease with depth into the landfill. The compression index, Cc, was observed to decrease from 1.0 to 0.3 with depth into the landfill. Settlement analyses were performed on the existing landfill, demonstrating that the variation of MSW compressibility with fill age or depth should be taken into account in the settlement prediction.     

Dechlorination of PCBs in the simulative transformer oil by microwave-hydrothermal reaction with zero-valent iron involved

The conventional hydrothermal reaction with iron powder, NaOH and H₂O as reactants was reported to occur at temperature above 423 K, and iron oxides (Fe₃O₄ and NaFeO₂) and hydrogen were produced. In this study, microwave heating was adopted to take the place of conventional heating to induce the hydrothermal reaction. Under microwave irradiation, NaOH and H₂O absorbed microwave energy by space charge polarization and dipolar polarization and instantly converted it into thermal energy, which initiated the hydrothermal reaction that involved with zero-valent iron. X-ray diffraction (XRD) analysis found Fe₃O₄/NaFeO₂ and confirmed the occurrence of microwave-induced hydrothermal reaction. The developed microwave-hydrothermal reaction was employed for the dechlorination of PCBs. Hexadecane containing 100 mg L⁻¹ of Aroclor1254 was used as simulative transformer oil, and the dechlorination of PCBs was evaluated by GC/ECD, GC/MS and ion chromatography. For PCBs in 10 mL simulative transformer oil, almost complete dechlorination was achieved by 750 W microwave irradiation for 10 min, with 0.3 g iron powder, 0.3 g NaOH and 0.6 mL H₂O added. The effects of important factors including microwave power and the amounts of reactants added, on the dechlorination degree were investigated, moreover, the dechlorination mechanism was suggested. Microwave irradiation combined with the common and cheap materials, iron powder, NaOH and H₂O, might provide a fast and cost-effective method for the treatment of PCBs-containing wastes.