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41.
以离子液体1-丁基磺酸-3-甲基咪唑三氟甲烷磺酸盐([BSO_3HMIm]OTf)为浸出剂,初步研究了WPCBs浸铜过程中锌和铅浸出率的影响因素。实验结果表明:铜、锌的浸出率随着WPCBs粒径的减小、H_2O_2溶液加入量的增大而增大,铜的浸出率随浸出温度的升高先增大后减小,锌的浸出率受浸出温度影响不大;铅的浸出率受5种因素影响不大,且总体处于较低水平。在WPCBs粒径为0.100~0.250 mm、离子液体加入量为60.0%(φ)、H_2O_2溶液加入量为7.5%(φ)、固液比为1∶15、浸出温度为50℃的条件下,铜、锌、铅的浸出率分别为99.84%,93.25%,22.46%。  相似文献   
42.
Thioarsenate formation upon dissolution of orpiment and arsenopyrite   总被引:5,自引:0,他引:5  
Thioarsenates were previously determined as dominant species in geothermal and mineral waters with excess sulfide. Here, we used batch leaching experiments to determine their formation upon weathering or industrial leaching of the arsenic-sulfide minerals orpiment (As2S3) and arsenopyrite (FeAsS) under different pH and oxygen conditions. Under acidic conditions, as expected based on their known kinetic instability at low pH, no thioarsenates formed in either of the two mineral systems. Under neutral to alkaline conditions, orpiment dissolution yielded mono-, di- and trithioarsenate which accounted for up to 43-55% of total arsenic. Thioarsenate formation upon arsenopyrite dissolution was low at neutral (4%) but significant at alkaline pH, especially under suboxic to sulfidic conditions (20-43%, mainly as monothioarsenate). In contrast to orpiment, we postulate that recombination of arsenite and sulfide in solution is of minor importance for monothioarsenate formation during alkaline arsenopyrite dissolution. We propose instead that hydroxyl physisorption lead to formation of As-OH-S surface complexes by transposition of hydroxyl anions to arsenic or iron sites. Concurrently formed ironhydroxides could provide re-sorption sites for the freshly released monothioarsenate. However, sorption experiments with goethite showed slower sorption kinetics of monothioarsenate compared to arsenite, but comparable with arsenate. The discovery that thioarsenates are released by natural weathering and industrial leaching processes and that, once they are released, have a higher mobility than the commonly-investigated species arsenite and arsenate requires future studies to consider them when assessing arsenic release in sulfidic natural or mining-impacted environments.  相似文献   
43.
It had been reported that iron and manganese oxides in steel slag enhanced the production of humic acid (HA) from low-molecular-weight compounds, such as phenolic acids, amino acids, and saccharides. In the present study, this function of steel slag was applied to the composting of raw organic wastes (ROWs). The degree of humification of HAs is an important factor in evaluating compost quality. Thus, HAs were extracted from the prepared composts and the humification parameters were determined, in terms of elemental compositions, acidic functional group contents, molecular weights, spectroscopic parameters from UV–vis absorption and 13C NMR spectra. The timing for adding steel slag affected the degree of humification of HAs in the composts. The weight average molecular weight of a HA when slag was added initially (29 kDa) was significantly higher than when slag was added after elevating the temperature of the compost pile (17–18 kDa). These results show that ROWs are decomposed to low-molecular-weight compounds after the pile temperature is elevated and the presence of slag enhances the polycondensation of these compounds to produce HAs with a higher degree of humification. Because the slag used in the present study contained several-tens ng g?1 to several μg g?1 of toxic elements (B, Cu, Cr, and Zn), leaching tests for these elements from the prepared composts were carried out. Levels for leaching boron from composts prepared by adding slag (0.2–0.4 mg L?1) were obviously higher than the corresponding levels without slag (0.05 mg L?1).  相似文献   
44.
有机酸土柱淋洗法修复重金属污染土壤   总被引:10,自引:1,他引:9  
通过室内模拟实验,采用土柱淋洗方法,研究草酸、柠檬酸、乙酸和酒石酸溶液对某电镀厂附近土壤中重金属的去除效果。探讨了淋洗剂浓度、淋洗次数和淋洗时间等对淋洗效果的影响,研究草酸淋洗前后土壤中重金属形态的变化。结果表明,淋洗过程中铬的去除效果明显滞后于铜、锌和镍3种重金属离子。1 mol/L的草酸在土水比为1∶1,淋洗5h,淋洗4次的条件下可以达到最佳淋洗效果,Cu、Zn、Ni和Cr的去除率分别是99.6%、66.98%、88.7%和18.23%。  相似文献   
45.
This study identifies the natural background, anthropogenic background and distribution of contamination caused by heavy metal pollutants in soil in Chunghua County of central Taiwan by using a finite mixture distribution model (FMDM). The probabilities of contaminated area distribution are mapped using single-variable indicator kriging and multiple-variable indicator kriging (MVIK) with the FMDM cut-off values and regulation thresholds for heavy metals. FMDM results indicate that Cr, Cu, Ni and Zn can be individually fitted by a mixture model representing the background and contamination distributions of the four metals in soil. The FMDM cut-off values for contamination caused by the metals are close to the regulation thresholds, except for the cut-off value of Zn. The receiver operating characteristic (ROC) curve validates that indicator kriging and MVIK with FMDM cut-off values can reliably delineate heavy metals contamination, particularly for areas lacking background information and high heavy metal concentrations in soil.  相似文献   
46.
生物质铬渣共热解工艺是新型的铬渣处理工艺,该工艺能有效地将铬渣中的Cr(Ⅵ)还原为Cr(Ⅲ).而由于共热解产物总铬含量较高,因此考察了铬渣与秸秆共热解过程中铬稳定性.通过考察共热解产物成分及形态分析、pH影响实验、淋洗实验及长期稳定性实验,对共热解铬渣的铬环境安全性进行评估.结果表明:(1)共热解温度对铬渣形态有较大影响,可交换态及碳酸盐结合态铬含量随共热解温度升高而逐渐降低,800℃时候可交换态铬降至<0.1%(质量分数,下同),碳酸盐结合态铬为1.2%;共热解后最稳定的残渣态铬含量随共热解温度升高而逐渐升高.(2)当pH>7时,两种共热解产物总铬溶出量极低,基本都小于6mg/kg;当pH≤7时,总铬的溶出量显著增加,最高超过500 mg/kg.但由于解毒铬渣的酸中和能力极强,因此铬释放风险较低.(3)共热解产物的总铬累积溶出量极低,根据拟合结果计算出其100年填埋时间的总铬溶出量不超过1.3 mg/kg.长期稳定性实验表明,自然堆置过程中共热解产物的Cr(Ⅵ)含量逐渐降低.  相似文献   
47.
废弃印刷线路板碘化法浸金研究   总被引:1,自引:0,他引:1  
针对碘化法从废弃印刷线路板中提取金的工艺设计,分别考察了碘的质量分数、n(I2)/n(I-)比值、固液比、双氧水的质量分数、pH值、浸出时间和浸出温度对金浸出率的影响。结合正交设计优化实验方法,提出了从废弃印刷线路板中碘化法浸取金的最佳工艺条件:碘的质量分数为1.1%,n(I2)∶n(I-)=1∶10,双氧水的质量分数为1.5%,浸出时间4 h,固液比为1∶10,浸出温度为常温(25℃),溶液pH值为中性,此时金浸出率可达97.5%。  相似文献   
48.
通过模拟煅烧试验制取水泥熟料,参照JGJ 55-2000(《普通混凝土配比设计规程》)制取混凝土样品,参考SR003.1和NEN 7375浸出试验,分别研究液固比对粒状及块状混凝土样品中重金属(Cr、Ni和As)释放的影响。结果表明,在不同液固比条件下粒状混凝土中的重金属浸出浓度为Cr>Ni>As,Cr、As浸出浓度基本保持不变,分别为2 500 μg/L左右和5~6 μg/L,Ni在液固比(L∶S)<6时,浸出浓度随着液固比的增加而降低,在L∶S>6时,浸出浓度较稳定,为35.7~41.5 μg/L;浸出量均随着液固比的增加而增大。液固比(L∶S)<10时,块状混凝土中重金属累积释放量及扩散系数均随液固比的增加而增大,当L∶S>10时两者基本保持不变。  相似文献   
49.
电解锰渣中锰的浸出条件及特征   总被引:2,自引:1,他引:1  
采用水洗-酸解法回收电解锰渣中锰,探讨了清水量、酸量以及温度在不同阶段对锰浸(洗)出条件的影响,分析了回收锰的主要因素及浸出特征。实验结果表明,50 g电解锰渣经m渣∶m水=1∶10的清水水洗后,采用10%的硫酸在70℃的水浴温度下酸解2 h,Mn2+浸出量为1.673 g,回收率达到97.3%,而温度和酸度对锰离子的浸出影响明显,酸度调控可有效分离酸浸锰液中金属成分,为减少电解锰渣环境污染的同时,实现电解锰渣资源化利用。  相似文献   
50.
The integrated modelling system INITIATOR was applied to a landscape in the northern part of the Netherlands to assess current nitrogen fluxes to air and water and the impact of various agricultural measures on these fluxes, using spatially explicit input data on animal numbers, land use, agricultural management, meteorology and soil. Average model results on NH3 deposition and N concentrations in surface water appear to be comparable to observations, but the deviation can be large at local scale, despite the use of high resolution data. Evaluated measures include: air scrubbers reducing NH3 emissions from poultry and pig housing systems, low protein feeding, reduced fertilizer amounts and low-emission stables for cattle. Low protein feeding and restrictive fertilizer application had the largest effect on both N inputs and N losses, resulting in N deposition reductions on Natura 2000 sites of 10% and 12%, respectively.  相似文献   
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