A survey on the temporal and spatial distribution of perchlorate in the Potomac River

Samples of river water and treated drinking water were obtained from eight sites along the Potomac River between western Maryland and Washington DC. Samples were collected each month from October 2007 to September 2008 and analyzed for perchlorate by ion chromatography/mass spectrometry. Data on anions were also collected for seven of the twelve months. Data were analyzed to identify spatial and temporal patterns for the occurrence of perchlorate in the Potomac. Over the year of sampling, the largest monthly increase occurred from June to July, with levels then decreasing from July to September. Samples from the period between December and May had lower perchlorate concentrations, relative to the remainder of the study year. Spatially, higher levels of perchlorate were found at sites located in west-central Maryland, the eastern panhandle of West Virginia, and central northern Virginia, with levels decreasing slightly as the Potomac approaches Washington DC. Within the sampling boundaries, river (untreated) water perchlorate concentrations ranged from 0.03 μg L(-1) to 7.63 μg L(-1), averaged 0.67 ± 0.97 μg L(-1) over the year-long period and had a median value of 0.37 μg L(-1). There was no evidence that any of the existing drinking water treatment technologies at the sampling sites were effective in removing perchlorate. There were no correlations found between the presence of perchlorate and any of the anions or water quality parameters examined in the source water with the exception of a weak positive correlation with water temperature. Results from the summer (June-August) and fall (September-November) months sampled in this study were generally higher than from the winter and spring months (December-May). All but one of the locations had annual average perchlorate levels below 1 μg L(-1); however, 7 of the 8 sites sampled had river water perchlorate detections over 1 μg L(-1) and 5 of the 8 sites had treated water detections over this level.     

Distribution features of biological hazardous pollutants in residential environments in Korea

This research has been conducted continuously since 2009 as part of a cohort of studies examining relationships between asthma and genetic factors, dietary habits, and environmental factors. Based on data from environmental research on house dust mites and endotoxins, which are widely known as pollutants in bedding that cause asthma in pregnant women and children, this work was conducted to obtain basic data that can be used in future cohort studies that analyze links between distribution of biological hazards and physical features of residential environments. The detection rates of house dust mite allergens, Der p1 and Der f1, were 52.7 and 86.5 %, respectively, indicating that Der f1 is a dominant species in domestic indoor environments. According to comparisons between concentrations of house dust mites and endotoxins in bedding of pregnant women and children, Der p1 and endotoxins showed significantly lower concentrations in bedding of pregnant women compared with those in bedding of children, whereas Der f1 showed no significant difference in concentration according to bedding.     

KOH活化花生壳生物质炭对亚甲基蓝吸附性能研究

以花生壳生物质炭(P-BC)为原料,KOH为活化剂,采用化学活化法制得活化生物质炭(K-BC),通过考察对亚甲基蓝的吸附性能,研究了花生壳生物质炭的最佳活化条件,并利用N2吸附-脱附实验、SEM等对最佳活化条件下的生物质炭进行表征.结果表明,K-BC活化的最佳条件为碱炭比为1.5:1,活化温度为800℃,活化时间为90 min,此时K-BC的比表面积达到597.93 m2/g,总孔容达到0.76 cm3/g.并考察了亚甲基蓝初始浓度、pH等对K-BC吸附亚甲基蓝的影响,随着初始浓度的增加,吸附平衡时间显著延长,亚甲基蓝去除率显著降低;当pH=6时,K-BC对亚甲基蓝的吸附量最大;K-BC对亚甲基蓝的吸附动力学曲线符合伪二阶动力学模型,吸附平衡时K-BC对亚甲基蓝的吸附能力为80~149.95 mg/g.     

Natural and anthropogenic influences on heavy metals in airborne particles over the Korean Peninsula

Six monitoring stations were selected to characterize the variations in airborne concentrations of heavy metals in South Korea between 1999 and 2012. Three stations represented higher concentrations, and three represented lower concentrations. The heavy metals monitored at these stations include cadmium, chromium, copper, iron (Fe), lead, manganese (Mn), and nickel. During the study period, concentrations of heavy metals at many stations, including those around the Seoul metropolitan area, showed a decreasing trend. However, concentrations of Mn and Fe that are primarily of crustal origin increased at four of the six stations. Some stations were significantly affected by emissions from the local industrial complex (IC), and heavy metal concentrations at those stations were relatively high even in summer. Many heavy metal concentrations were higher in spring than in winter, but wintertime concentrations of Cr and Pb were higher at the stations representing lower concentrations due to the dominant influence of combustion emissions. At stations less affected by emissions from the IC, concentrations of Fe and Mn that are predominantly crustal in origin were higher in spring, when Asian dust (AD) events are most frequent. Although Mn concentrations were also high at stations within the steelmaking IC during AD periods, they were much higher during non-AD periods due to local emissions. Variations in heavy metal concentrations, which are heavily influenced by emissions from the IC, warrant individual analysis because their emission characteristics differ from those of typical cases.     

金属铁离子对农田土壤氮转化影响分析

以长春伊通河河谷阶地上部的农田土为研究对象,选用铁离子作为氮转化的一种影响因素,定性研究了不同浓度的铁离子对硝态氮、亚硝态氮、铵态氮三氮的变化影响。并且在建立方程组之后计算平衡常数,证明了铁的氧化作用,与实验所得相符合：铁促进铵态氮的吸附、促进硝化反应的进行。从实验和理论的角度说明了铁在三氮转化中起的作用,为进一步研究锰铁离子对氮转化的定量影响和氮素污染地下水的预测和定量评价提供科学依据。     

煤中易挥发有毒痕量元素及其在燃烧过程中的行为

本文综述了煤中易挥发有毒痕量元素汞、砷、硒在煤中的赋存形式 ,在燃烧过程中的蒸发和化学反应等行为 ,指出了在目前研究燃煤过程中有毒痕量元素所存在的问题和需要努力加强的研究方向     

光氧化吸附矿井水中微量有机物试验研究

针对目前煤矿矿井水资源化过程中存在有机污染物的问题，考察了采用紫外光氧化分解的机理及影响因素。结果表明：紫外光对矿井水中有机物（主要是乳化油）有一定的氧化分解能力，能有效地促使有机物大分子破裂，有利于活性炭的吸附处理。在合理的工艺条件下，可使水中有机物去除率达到95%以上。     

粉煤灰/工业污泥烧结陶粒的制备与应用

以粉煤灰和工业污水处理站的剩余污泥为主要原材料，采用烧结法研制复合陶粒。分析了不同配方和不同烧结温度对陶粒性能的影响，以陶粒吸水率．容重为评价指标确定最佳配比和最佳烧结温度。提出用陶粒铺设景观水底，治理城市水体．并对其进行了可行性分析。粉煤灰／污泥陶粒的容重为0．79～0．9g／cm^3，吸水率为68．95％-80．01％。陶粒对水中氨氮和总磷吸附容量分别为0．03～0．05mg／g和0．01-0.02mg／g。     

Assessing soil and groundwater contamination in a metropolitan redevelopment project

The purpose of this study was to assess contaminated soil and groundwater for the urban redevelopment of a rapid transit railway and a new mega-shopping area. Contaminated soil and groundwater may interfere with the progress of this project, and residents and shoppers may be exposed to human health risks. The study area has been remediated after application of first remediation technologies. Of the entire area, several sites were still contaminated by waste materials and petroleum. For zinc (Zn) contamination, high Zn concentrations were detected because waste materials were disposed in the entire area. For petroleum contamination, high total petroleum hydrocarbon (TPH) and hydrocarbon degrading microbe concentrations were observed at the depth of 7 m because the underground petroleum storage tank had previously been located at this site. Correlation results suggest that TPH (soil) concentration is still related with TPH (groundwater) concentration. The relationship is taken into account in the Spearman coefficient (α).     

Effect of temperature on single and competitive adsorptions of Cu(II) and Zn(II) onto natural clays

This study conducted a combined adsorption-sequential extractionanalysis (CASA), by which five phases (i.e., exchangeable, carbonate, Mn-Oxide, organic, and Fe-Oxide phases) of adsorbed heavy metals were analyzed, to investigate temperature effects on single and competitive adsorptions of Zn(II) and Cu(II) ontonatural clays. In the case of single adsorption of Zn, the exchangeable phase adsorption decreased from 65 to 40%, but thecarbonate phase adsorption increased from 30 to 40%, with an increase in temperature from 15 to 55 °C. However, in itscompetitive adsorption with Cu, Zn was mostly present in the exchangeable phase (over 90%), and with an increase in temperature, the exchangeable phase adsorption decreased only 10%. In the case of Cu, over 50% among the total amount of adsorption was present in the carbonate phase in both cases ofsingle and competitive adsorptions. The carbonate phaseadsorption of Cu increased from 56 to 61% and from 60 to 66% in single and competitive adsorptions, respectively, with atemperature increase. These results show that in the case of Zn,the major mechanism of retention in natural clay soils might beexchangeable phase adsorption, especially in the case of competitive adsorption with Cu. However, in the case of Cu, the major mechanism might be carbonate phase adsorption, which is known to be a more immobile phase than exchangeable phase adsorption. It seems that the adsorption of Zn and Cu onto natural clays is an endothermic reaction, which represents thatthe adsorption equilibrium constants and capacities increase with a temperature increase, with the exception of exchangeablephase adsorption.