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1.
Preliminary studies on potential remediation of acid mine drainage‐impacted soils by amendment with drinking‐water treatment residuals 下载免费PDF全文
Mining operations result in a wide range of environmental impacts: acid mine drainage (AMD) and acid sulfate soils being among the most common. Due to their acidic pH and high soluble metal concentrations, both AMD and acid sulfate soils can severely damage the local ecosystems. Proper post‐mining management practices are necessary to control AMD‐related environmental issues. Current AMD‐impacted soil treatment technologies are rather expensive and typically not environmentally sustainable. We conducted a 60‐day bench‐scale study to evaluate the potential of a cost‐effective and environment‐friendly technology in treating AMD‐impacted soils. The metal binding and acid‐neutralizing capacity of an industrial by‐product, drinking water treatment residuals (WTRs) were used for AMD remediation. Two types of locally generated WTRs, an aluminum‐based WTR (Al‐WTR) and a lime‐based WTR (Ca‐WTR) were used. Highly acidic AMD‐impacted soil containing very high concentrations of metals and metalloids, such as iron, nickel, and arsenic, was collected from the Tab‐Simco coal mine in Carbondale, Illinois. Soil amendment using a 1:1 Al‐ and Ca‐WTR mix, applied at 5 and 10 percent rates significantly lowered the soluble and exchangeable fractions of metals in the AMD‐impacted soil, thus lowering potential metal toxicity. Soil pH increased from an extremely acidic 2.69 to a near‐neutral 6.86 standard units over the 60‐day study period. Results from this preliminary study suggest the possibility of a successful scale‐up of this innovative, cost‐effective, and environmentally sustainable technology for remediating AMD‐impacted acid sulfate soils. 相似文献
2.
The word “textile” means to weave and was taken from the Latin word “texere.” Nowadays, textiles not only fulfill humankind's basic necessity for clothing, they also allow individuals to make fashion statements. As one of the oldest industries, the textile industry occupies a unique place in India. It is responsible for 14% of the total industrial manufacture in India. However, the textile industry is also considered to be one of the biggest threats to the environment. Pretreatment, dyeing, printing, and finishing operations are among the various stages of the industrial textile manufacturing process. These fabrication operations not only utilize huge quantities of power and water, they also generate considerable amounts of waste. The textile industry utilizes a number of dyes, chemicals, and other materials to impart the required qualities to the fabrics. These operations produce a significant amount of effluents. The quality of effluents is such that they cannot be put to other uses, and they can create environmental problems if they are disposed of without appropriate treatment. This review discusses different textile processing stages, pollution problems associated with these stages, and their eco‐friendly alternatives. Textile wet processing is described in detail, as it is the key process in the industry and it also generates the greatest amount of pollutants in textile processing. The environmental impact of textile effluents is discussed, as textile effluents not only impose negative effects on the quality of water and soil, they also imperil plant and animal health. In this paper, various methods for treating textile effluents are described. Discussion of physical, chemical, biological, and advanced treatment technologies of effluent treatment are included in this paper. 相似文献
3.
Chlorinated ethenes such as trichloroethene (TCE), cis‐1,2‐dichloroethene (cis‐1,2‐DCE), and vinyl chloride along with per‐ and polyfluoroalkyl substances (PFAS) have been identified as chemicals of concern in groundwater; with many of the compounds being confirmed as being carcinogens or suspected carcinogens. While there are a variety of demonstrated in‐situ technologies for the treatment of chlorinated ethenes, there are limited technologies available to treat PFAS in groundwater. At a former industrial site shallow groundwater was impacted with TCE, cis‐1,2‐DCE, and vinyl chloride at concentrations up to 985, 258, and 54 µg/L, respectively. The groundwater also contained maximum concentrations of the following PFAS: 12,800 ng/L of perfluoropentanoic acid, 3,240 ng/L of perfluorohexanoic acid, 795 ng/L of perfluorobutanoic acid, 950 ng/L of perfluorooctanoic acid, and 2,140 ng/L of perfluorooctanesulfonic acid. Using a combination of adsorption, biotic, and abiotic degradation in situ remedial approaches, the chemicals of concern were targeted for removal from the groundwater with adsorption being utilized for PFAS whereas adsorption, chemical reduction, and anaerobic biodegradation were used for the chlorinated ethenes. Sampling of the groundwater over a 24‐month period indicated that the detected PFAS were treated to either their detection, or below the analytical detection limit over the monitoring period. Postinjection results for TCE, cis‐1,2‐DCE, and vinyl chloride indicated that the concentrations of the three compounds decreased by an order of magnitude within 4 months of injection, with TCE decreasing to below the analytical detection limit over the 24‐month monitoring period. Cis‐1,2‐DCE, and vinyl chloride concentrations decreased by over 99% within 8 months of injections, remaining at or below these concentrations during the 24‐month monitoring period. Analyses of Dehalococcoides, ethene, and acetylene over time suggest that microbiological and reductive dechlorination were occurring in conjunction with adsorption to attenuate the chlorinated ethenes and PFAS within the aquifer. Analysis of soil cores collected pre‐ and post‐injection, indicated that the distribution of the colloidal activated carbon was influenced by small scale heterogeneities within the aquifer. However, all aquifer samples collected within the targeted injection zone contained total organic carbon at concentrations at least one order of magnitude greater than the preinjection total organic carbon concentrations. 相似文献
4.
土壤污染修复产业是环保产业新一轮发展的重点,其市场规模在未来可能是千亿级或万亿级。我国土壤污染修复产业发展面临要素支撑能力不强、配套基础条件薄弱和环境监管基础能力不足三大难题。需要从强化土壤污染修复人才的引进、储备和培养,以科技创新能力提升支撑土壤污染修复产业的发展,拓展投融资渠道、夯实土壤污染修复产业发展的资金保障三方面入手加强土壤污染修复产业的要素支撑能力建设;培育和壮大土壤污染修复产业集群,推进污染土壤污染修复环境管理与工程示范;完善土壤污染修复产业配套基础条件;加强环境监管能力建设,完善土壤环境管理体系,提升项目管理水平。 相似文献
5.
CaO2具有很好的稳定性,可在水和土壤中逐步分解生成H2O2成为氧化反应的氧化剂,已作为H2O2的替代物用于环保领域的研究中。介绍了CaO2的作用机理,综述了CaO2用于处理含卤代物、染料、抗生素、苯系物等废水的研究进展,以及CaO2用于治理含石油烃、多环芳烃、苯系物和农药的污染土壤的研究进展。提出未来的研究方向:充分利用CaO2水解生成O2和H2O2的特性,探索化学与生物联合修复技术;探究CaO2与其他氧化剂联用技术,从而增加CaO2修复技术的适用性和经济性。 相似文献
6.
Fenton法和类Fenton法降解土壤中的二苯砷酸 总被引:1,自引:0,他引:1
本文对Fenton法与类Fenton法降解土壤中的二苯砷酸(diphenylarsinic acid,DPAA)进行了研究.考察了H2O2投加量和催化剂种类(Fe2+/Fe3+)对红壤及黑土中DPAA降解效果的影响,并采用高效液相色谱-质谱联用法(HPLC-MS/MS)对降解中间产物进行了初步鉴定.结果显示,针对红壤与黑土分别采用类Fenton法与Fenton法,在H2O2投加浓度为1 mol·L-1,含铁催化剂浓度为0.25 mol·L-1,土水比为1∶3,反应时间为1h的条件下,红壤及黑土中DPAA的降解率均可达到65%以上.HPLC-MS/MS的分析结果表明,DPAA可脱苯环形成降解产物苯砷酸(phenylarsinic acid,PAA),而PAA进一步氧化生成无机砷,这可能是Fenton/类Fenton法降解DPAA的途径之一. 相似文献
7.
通过投加抗坏血酸(C6H8O6)或铁系还原剂(FeCl2,(NH4)2Fe(SO4)2,FeS)对重庆某化工厂的Cr污染土壤进行修复。除FeS外,其余3种还原剂对土壤中Cr(Ⅵ)的还原率均达80%以上,稳定效率均超73%,且投加量为理论值3倍和4倍时的效果相差不大。C6H8O6相比于铁系还原剂表现出更好的长期稳定性,4~30 d的Cr(Ⅵ)浸出质量浓度均低于《生活垃圾填埋场污染控制标准》(GB 16889—2008)中Cr(Ⅵ)的浸出限值(1.5 mg/L)。投加3倍理论值C6H8O6的土壤在30 d时的Cr(Ⅵ)浸出质量浓度仅为0.83 mg/L,稳定效率高达98.3%。除FeS外,其余3种还原剂均显著增加了土壤中Cr的残渣态占比。FeCl2和(NH4)2Fe(SO4)2会导致土壤pH降低。4种还原剂均未对土壤晶体结构产生明显影响。 相似文献
8.
9.
在田间试验条件下,考察不同钝化材料对农田Cd轻度污染水稻修复效果及稻麦轮作后第二年水稻修复后效。结果表明,在轻度Cd污染农田中,各钝化材料处理均能不同程度降低土壤有效态Cd含量和水稻籽粒中Cd含量。其中,在钝化材料施用当季和稻麦轮作后第二季水稻中修复效果最好的处理为中量纳米材料处理和石灰配施中量纳米材料处理,这两种处理对土壤有效态Cd含量降低率分别为50.94%和47.15%,对水稻籽粒中Cd含量降低率分别为73.74%和69.41%。 相似文献
10.
磷基材料对土壤Pb有良好的稳定化效果.利用Meta分析法筛选汇总了1997~2022年磷基材料稳定土壤Pb的90篇文献,从土壤性质、稳定化工艺条件和磷基材料类型这3个方面量化分析了磷基材料对土壤Pb的稳定化率、赋存形态转化和对土壤pH的影响.结果表明,从土壤性质来看,土壤碱性越强(pH≥7.5)、土壤ω(Pb)越低(≤500 mg ·kg-1)和土壤ω(有机质)越高(>0.5%)时,越有利于磷基材料对土壤Pb的稳定化,稳定化率分别为75.21%、34.97%和93.12%.从稳定化工艺条件来看,磷基材料添加量较高(≥10%)、含水率较高(>50%)、养护时间较长(≥30d)和养护温度较高(≥40℃)时,更有利于土壤Pb的稳定化,稳定化率可分别达到80.65%、84.98%、79.39%和41.44%.从磷基材料类型来看,可溶性磷基材料对土壤Pb有很高稳定化率(96.24%);其使土壤可交换态Pb和碳酸盐结合态Pb向残渣态Pb转化的转化率达到95.93%;可溶性磷基材料多呈酸性,对土壤pH的降低率为7.27%,难溶性磷基材料多呈碱性,对土壤pH的增加率为3.63%.综上,在土壤pH≥7.5、土壤ω(Pb)≤500 mg ·kg-1、土壤ω(有机质)>0.5%、可溶性磷基材料添加量≥10%、含水率>50%、养护时间≥30 d和养护温度≥40℃时,磷基材料对土壤Pb的稳定化效果较好.可见在实际Pb污染土壤修复过程中,为提高Pb稳定化率,需综合考虑土壤性质、稳定化工艺条件和磷基材料类型等因素的影响. 相似文献