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Various solid phase extraction (SPE) cartridges were investigated for speciation of arsenite [As(III)], arsenate [As(v)], monomethylarsonic acid (MMA) and dimethylarsinic acid (DMA). Cartridges containing different types of sorbent materials were tested for arsenic retention and elution characteristics. Alumina cartridges were found to completely retain all the four target arsenic species, and are suitable for removal and preconcentration purposes. For speciation analysis, different arsenic species were separated on the basis of their selective retention on and elution from specific cartridges. DMA was retained on a resin-based strong cation exchange cartridge and eluted with 1.0 M HCl. MMA and As(v) were both retained on a silica-based strong anion exchange cartridge and sequentially eluted with 60 mM acetic acid (for MMA) and 1.0 M HCl [for As(v)]. As(III) was not retained on either cartridge and remained in solution. Arsenic species in solution and those eluted from the cartridges were subsequently quantified by using flow injection with hydride generation atomic fluorescence spectrometry (FI-HGAFS) and hydride generation atomic absorption spectrometry (FI-HGAAS). A detection limit of 0.05 microg L(-1) arsenic in water sample was achieved using HGAFS. An application of the method was demonstrated at a drinking water treatment facility. As(III) and As(v) species were determined in water at various stages of treatment. The method is suitable for routine determination of trace levels of arsenic in drinking water to comply with more stringent environmental regulations. 相似文献
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电化学氧化法处理垃圾渗滤液纳滤浓缩液 总被引:2,自引:0,他引:2
实验利用电化学氧化法处理垃圾渗滤液纳滤浓缩液,以提高废水的可生化性。研究考察了水力停留时间、进水流量、循环流量、电流强度和原水氯离子浓度对有机物去除的影响。研究结果表明,电化学氧化法的最佳运行条件如下:水力停留时间为 3 h,进水流量为1 m3/h,循环流量为15 m3/h,电流强度为420 A。在上述条件下,原水COD浓度从3 100 mg/L降到1 311.3 mg/L,去除率达到57.7%,BOD/COD值由0.03提升至0.31。氯离子对电解有促进作用,但原水氯离子浓度超过5 000 mg/L,不需要外加工业盐。 相似文献
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采用热重分析的方法对吸收剂的再生反应进行研究,说明了燃煤飞灰负载钾基CO2吸收剂的制备方法,探讨了在不同升温速率下燃煤飞灰负载钾基CO2吸收剂和纯KHCO3的再生反应特性。结果表明: 燃煤飞灰负载吸收剂的峰值失重速率为0.13~0.73 mg?min-1,在升温速率为20 ℃?min-1时,反应温度区间最小,为94.34 ℃;采用多种分析方法对吸收剂的受热分解反应进行动力学分析,纯KHCO3的反应活化能为85.7~92.0 kJ·mol-1;燃煤飞灰负载钾基CO2吸收剂的反应活化能为66.2~69.4 kJ·mol-1,随着转化率上升,2种样品的活化能均先减小后增大。燃煤飞灰负载钾基吸收剂再生反应的活化能小于纯KHCO3的活化能,说明将KHCO3负载于燃煤飞灰上有利于再生反应的进行。 相似文献
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<正>Mercury is a global pollutant due to its widespread use,emission,and long-range transport(Blum,2013;Pacyna et al.,2010).It is considered a priority pollutant due to its neurological toxicity,persistence,and bioaccumulation(Pacyna et al.,2010;Sharma et al.,2015).Mercury pollution can occur when products that contain mercury are improperly disposed of and mercury is released into the air,water,and soil(Zhang and Wong,2007).An estimated 22%of the annual world usage of mercury is in electrical equipment such as batteries,thermometers,and discharge lamps,and electronic devices such as monitors and 相似文献
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Soils from two typical tidal salt marshes with varied salinity in the Yellow River Delta wetland were analysed to determine possible effects of salinity on soil carbon sequestration through changes in soil microbiology. The mean soil respiration (SR) of the salt water–fresh water mixing zone (MZ) was 2.89 times higher than that of the coastal zone (CZ) (4.73 and 1.63?μmol?m?2?s?1, respectively, p?.05), and soil dehydrogenase activity was the main microbial factor influencing SR. In addition to the higher soil microbial biomass, the MZ had more β-Proteobacteria than the CZ, as well as some specific bacteria with strong heterotrophic metabolic activity such as Pseudomonas sp. and Limnobacter sp. that might have led to its higher dehydrogenase activity and respiratory rates. Additionally, the CZ possessed more Halobacteria and Thaumarchaeota with the ability to fix CO2 than the MZ. Significantly lower soil salinity in MZ (4.25?g?kg?1) was suitable for β-Proteobacteria, but detrimental for Halobacteria compared with CZ (7.09?g?kg?1, p?.01), which might lead to the lower microbial decomposition capacity of soils in CZ. As a result, the CZ has a higher soil organic carbon content than the MZ. 相似文献