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1.
模拟土壤淋洗废液中重金属的选择性去除与淋洗液的回收研究 总被引:1,自引:0,他引:1
土壤淋洗废液中污染物的选择性去除是实现淋洗液回收的关键.本文以硫化钠(Na2S)、乙基黄原酸钾(PEX)、二甲基二硫代氨基甲酸钠(DTC)作为重金属沉淀剂处理电子垃圾污染土壤模拟淋洗废液,在筛选出Na2S作为理想重金属沉淀剂的基础上,研究初始pH值、反应温度、沉淀剂浓度等因素对Na2S分离络合态重金属的影响,并通过软件模拟和产物表征等方式推测反应机理.结果表明:Na2S对柠檬酸络合态重金属的分离顺序依次为Cu、Pb、Cd,符合硫化物溶度积原则;反应温度、初始pH值对Na2S处理络合态重金属无显著影响,重金属去除率均保持在90%以上,柠檬酸的回收率约为95%;Visual MINTEQ模拟结果显示,S2-投加前液相中重金属主要以H2CA-、HCA2-和CA3-结合形式存在,S2-投加后液相中重金属则以HS-和S2-结合形式存在;扫描电镜及能谱(SEM-EDS)表明,S2-与金属阳离子按物质的量比1:1生成硫化物沉淀物,沉淀主要呈团聚、成簇和圆片状存在;X射线衍射(XRD)分析结果表明,沉淀产物中存在CuS、CdS、PbS和CuPbS2.本研究结果可为化学沉淀法处理重金属污染土壤淋洗废液提供技术参考. 相似文献
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介绍以铝矾土提取硫酸铝废渣和氧氯化锆副产废碱液为原料生产泡花碱 ,然后利用一次造粒法生产五水偏硅酸钠新工艺确定影响产品质量指标工艺因素。小试试验产品质量指标达到HG/T2 5 6 8- 94要求 ,工艺成本低 ,避免废碱液及废渣排放对环境的污染。 相似文献
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Water solubility enhancements of naphthalene( Naph), phenantherene(Phen) and pyrene(Py) in sodium castor oil sulfonate(SCOS) microemulsions were evaluated. The apparent solubilities of PAHs are linearly propertional to the concentrations of SCOS microemulsion, and the enhancement extent by SCOS solutions is greater than that by ordinary surfactants on the basis of weight solubilization ratio(WSR). ThelogKcm values of Naph, Phen, and Py are 3.13, 4.44 and 5.01 respectively, which are about the same as the logKow values. At 5000 mg/L of SCOS conccentration, the apparent solubilities are 8.80, 121, and 674 times as the intrinsic solubilities for Naph, Phen, and Py. The effects of inorganic ions and temperature on the solubilization of solutes are also investigated. The solubilization is improved with a moderate addition of Ca^2 , Na^ , NH4^ and the mixture of Na^ , K^ , Ca^2 , Mg^2 and NH4^ . WSR values are enhanced by 22.0% for Naph,23.4% for Phen, and 24.6% for Py with temperature increasing by 5~C. The results indicated that SCOS microemulsions improve the performance of the surfactant-enhanced remediation(SER) of soil, by increasing solubilities of organic pollutants and reducing the level of surfactant pollution and remediation expenses. 相似文献
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Tohru Kamo Kanji Takaoka Junichiro Otomo Hiroshi Takahashi 《Journal of Material Cycles and Waste Management》2006,8(2):109-115
Steam gasification of dehydrochlorinated poly(vinyl chloride) (PVC) or activated carbon was carried out in the presence of
various alkali compounds at 3.0 MPa and 560°C–660°C in a batch reactor or in a semi-batch reactor with a flow of nitrogen
and steam. Hydrogen and sodium carbonate were the main products, and methane and carbon dioxide were the minor products. Yields
of hydrogen were high in the presence of sodium hydroxide and potassium hydroxide. The acceleration effect of the alkali compounds
on the gasification reaction was as follows: KOH > NaOH > Ca(OH)2 > Na2CO3. The rate of gasification increased with increasing partial steam pressure and NaOH/C molar ratio. However, the rate became
saturated at a molar ratio of NaOH/C greater than 2.0. 相似文献
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马建华 《中国环境管理干部学院学报》2005,15(1):38-41
采用顶空气相色谱法测定食品中甜蜜素含量,探讨了气液相平衡条件及色谱条件的选择,实验结果表明甜蜜素的标准溶液在0.1-0.4μg/l范围内具有良好的线性关系,回收率为87.5%-101.8%,相对标准偏差为2.6%. 相似文献
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Simultaneous removal of Cu(II) and Cr(VI) by Mg–Al–Cl layered double hydroxide and mechanism insight
Mg–Al–Cl layered double hydroxide (Cl-LDH) was prepared to simultaneously remove Cu(II) and Cr(VI) from aqueous solution. The coexisting Cu(II) (20 mg/L) and Cr(VI) (40 mg/L) were completely removed within 30 min by Cl-LDH in a dosage of 2.0 g/L; the removal rate of Cu(II) was accelerated in the presence of Cr(VI). Moreover, compared with the adsorption of single Cu(II) or Cr(VI), the adsorption capacities of Cl-LDH for Cu(II) and Cr(VI) can be improved by 81.05% and 49.56%, respectively, in the case of coexisting Cu(II) (200 mg/L) and Cr(VI) (400 mg/L). The affecting factors (such as solution initial pH, adsorbent dosage, and contact time) have been systematically investigated. Besides, the changes of pH values and the concentrations of Mg2+ and Al3+ in relevant solutions were monitored. To get the underlying mechanism, the Cl-LDH samples before and after adsorption were thoroughly characterized by X-ray powder diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. On the basis of these analyses, a possible mechanism was proposed. The coadsorption process involves anion exchange of Cr(VI) with Cl− in Cl-LDH interlayer, isomorphic substitution of Mg2+ with Cu2+, formation of Cu2Cl(OH)3 precipitation, and the adsorption of Cr(VI) by Cu2Cl(OH)3. This work provides a new insight into simultaneous removal of heavy metal cations and anions from wastewater by Cl-LDH. 相似文献