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以重金属污染土壤为研究对象,比较了铁屑、蒙脱石、碳酸钙和羟基磷灰石4种稳定剂对土壤中Pb,Zn,Cd,Cu 4种重金属的稳定效果。实验结果表明,4种稳定剂稳定效率的大小顺序为:羟基磷灰石碳酸钙蒙脱石铁屑。当稳定剂质量分数为10%时,羟基磷灰石、碳酸钙、蒙脱石和铁屑对Pb,Zn,Cd,Cu 4种重金属的平均稳定效率分别为99.63%,98.53%,97.15%,86.95%。未加稳定剂时,土壤中的Pb以残渣态为主,Zn以残渣态和可交换态为主,Cd以残渣态为主,Cu以残渣态和可交换态为主;加入稳定剂后,土壤中4种金属可交换态的所占比例(简称占比)均显著降低,还原态的占比明显增大,残渣态的占比略有增大,氧化态的占比基本保持不变。 相似文献
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以重金属污染土壤为研究对象,比较了铁屑、蒙脱石、碳酸钙和羟基磷灰石4种稳定剂对土壤中Pb,Zn,Cd,Cu 4种重金属的稳定效果。实验结果表明,4种稳定剂稳定效率的大小顺序为:羟基磷灰石﹥碳酸钙﹥蒙脱石﹥铁屑。当稳定剂质量分数为10%时,羟基磷灰石、碳酸钙、蒙脱石和铁屑对Pb,Zn,Cd,Cu 4种重金属的平均稳定效率分别为99.63%,98.53%,97.15%,86.95 %。未加稳定剂时,土壤中的Pb以残渣态为主,Zn以残渣态和可交换态为主,Cd以残渣态为主,Cu以残渣态和可交换态为主;加入稳定剂后,土壤中4种金属可交换态的所占比例(简称占比)均显著降低,还原态的占比明显增大,残渣态的占比略有增大,氧化态的占比基本保持不变。 相似文献
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喀斯特山区燃煤电厂土壤重金属污染评价 总被引:3,自引:0,他引:3
选取地处贵州省喀斯特山区的金沙电厂为研究对象,对电厂周围的表层土壤、蔬菜(莲花白)试样的重金属含量进行了测定,采用模糊数学法对土壤重金属污染进行了评价,采用富集系数法分析了莲花白对重金属的富集能力。实验结果表明:电厂周围表层土壤中Hg,As,Cd,Pb,Cu的平均含量分别达0.70,26.40,0.61,44.83,35.51 mg/kg,其中,Hg和Cd的平均含量分别为GB 15618—1995《土壤环境质量标准》中二级标准的1.40和2.03倍;电厂周围土壤受到较为严重的Hg,As,Cd污染,各个方向的重金属污染程度大小顺序为西北西东南西南东北东,总体趋势为西向大于东向;莲花白对土壤中Cd的富集作用较强,对其他重金属的富集作用较弱。 相似文献
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吴燕芳 《再生资源与循环经济》2013,6(5)
目前,我国重金属污染呈现出长期积累和近期集中爆发、历史遗留问题和新出现问题相交织的特点,重金属污染在环境中存在多、形态多,整治重金属污染是一项长期、复杂、艰巨的任务.重金属污染物极难降解,尤其是存在于水和土壤中的重金属兼具富集性,是不可逆转的.重点阐述了重金属污染土壤的修复技术研究进展及发展前景. 相似文献
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采用柠檬酸溶液对模拟电子垃圾污染土壤(简称污染土壤)中Cu,Pb,Cd 3种重金属进行淋洗实验,考察了柠檬酸溶液的浓度、柠檬酸溶液的pH、淋洗时间等对污染土壤中Cu,Pb,Cd的淋洗效果,探讨了柠檬酸溶液淋洗前后污染土壤中Cu,Pb,Cd 3种重金属各形态含量的变化。研究结果表明,在柠檬酸溶液的浓度0.100 mol/L、柠檬酸溶液的pH 5、淋洗时间1 440 min的适宜条件下,对污染土壤中Cu,Pb,Cd的去除率分别达到89.37%,72.11%,86.39%。柠檬酸溶液对3种重金属的去除主要是通过洗出酸可提取态(R1)和酸可还原态(R2)来实现的,每种重金属的R1和R2之和均占到其淋出总量的95%以上,而酸可氧化态(R3)和残渣态(R4)的含量淋洗前后基本无变化。 相似文献
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模糊综合评判法在区域土壤环境重金属污染评价中的应用 总被引:25,自引:1,他引:25
应用模糊数学中的模糊综合评判法,对华东某一区域土壤环境中的重金属污染程度进行了评价,运用多因子共同作用机理,对土壤环境质量的分级问题进行了探讨。 相似文献
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分别采用硫酸硝酸法、水平振荡法和醋酸缓冲溶液法制取气化炉渣的浸出液,考察了不同提取方式对浸出液中重金属质量浓度的影响。采用改进BCR连续提取法对气化炉渣中的重金属Cr,Zn,Cu,Pb,Ni,As,Cd的化学形态进行了分析。实验结果表明:煤气化工艺中的气化炉渣属第Ⅰ类一般工业固体废物;在3种提取方式中,醋酸缓冲溶液法的重金属浸出种类最多,且浸出量最大;Cd和Cr对环境具有较高的潜在危害性,Cu次之,Zn,Pb,Ni,As主要以残渣态形式存在,对环境的直接危害性较低。 相似文献
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土壤-植物系统重金属形态分析和生物有效性研究进展 总被引:62,自引:0,他引:62
介绍了土壤-植物系统中重金属连续提取的形态分析方法研究进展,同时归纳了影响重金属生物有效性的主要因素,如土壤性质、复合污染及根际环境等,并指出了需要解决的问题与今后的发展方向。 相似文献
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The SO4–S and NO3–N concentrations and pH in bulk precipitation, throughfall, stemflow and soil water for the 1994–2004 period were studied
in pine forests in Latvia (Rucava and Taurene Integrated Monitoring stations). The SO4–S and NO3–N concentrations decreased over the study period, simultaneously with a decrease of acidity in precipitation. The changes
were more evident in the western part of Latvia, probably due to declining long-range air pollution from West Europe. The
trend of decreasing sulphate concentrations and increasing pH in precipitation were not followed by respective changes in
soil water. In the upper soil horizon sulphate ion concentrations and acidity increased in soil water. Over the observation
period, nitrate concentrations also showed an increasing trend in soil water at Rucava and Taurene, but these changes were
not statistically significant. 相似文献
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改性淀粉的合成及其对重金属离子的捕集效果 总被引:3,自引:0,他引:3
以玉米淀粉为原料,经过交联、间接醚化、胺化以及cs:亲核加成反应,得到二硫代氨基甲酸基(DTC)改性淀粉(DTCS),并对其合成条件进行优化;考察了交联度、醚化温度、氯含量及胺化剂对DTCS捕集重金属离子效果的影响。优化后的DTCS合成条件:交联淀粉(CS)沉降积为30—34mL,醚化温度为80℃,氯质量分数为7.82%,胺化剂为二乙烯四胺。实验结果表明,DTCS对Cu^2+,Pb^2+,Zn^2+,Cd^2+,Ni^2+均有较好的去除效果,其对Cu^2+,Pb^2+,Zn^2+,Cd^2+,Ni^2+的饱和吸附量分别为0.85,0.83,0.65,0.74,0.47mmol/g。 相似文献
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采用离子交换膜电解技术处理铜冶炼过程产生的含氯及重金属的废酸。考察了废酸处理工艺、电解温度、电解时间、电流密度和催化剂的添加等条件对处理效果的影响。实验结果表明:采用先沉淀重金属后脱氯的废酸处理工艺,氯离子和铜离子的去除效果均较好;当以钛盐为催化剂时,在电解温度为40 ℃、电解时间为2.0 h、电流密度为825 A/m2的最佳工艺条件下,处理后废酸中的氯离子质量浓度为0.22 g/L,氯离子去除率为98.59%,铜离子质量浓度为0.45 g/L,铜离子去除率为95.08%,其他重金属大部分也得到有效去除。净化后的废酸可回用至铜冶炼的生产过程中。 相似文献
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The within-site correlations between soil respiration rates,lead (Pb), mercury (Hg) and cadmium (Cd) concentrations andorganic matter quality variables were investigated at four sites in southern Sweden. The aim was to study whether the within-site variation in heavy metal concentrations could beused to monitor biological effects of regional deposition of heavy metals. Two sites in the south-west, one in the mid-southof the country, and one in south-east were investigated. At the south-eastern, least contaminated, site there were no correlations between soil respiration rate, and either organicmatter quality variables or heavy metal concentrations. At the remaining sites, negative correlations were found between Pb andsoil respiration rate. However, at two of these three sites there was a covariation with cellulose that could account for these correlations. The within-site variation of pH and total nitrogen (N) was low, and did not show any correlative general trends with either respiration rate or heavy metals. Meta analysis showed that negative correlations between Pb or Hg, on the one hand, and cellulose or hemicellulose on the other weregenerally found in within-site investigations. However, this does not necessarily explain the correlation between Pb and soil respiration, as was shown for the southernmost site. A PLS model of soil respiration rates at this site, using allmeasured variables, including heavy metals, explained more variation than a model developed using only mor layer thickness,pH, carbohydrate, ash and nitrogen concentrations, as independent variables. Thus there is a risk of toxic effects from Pb even at the levels found in south-western Sweden today(>120 g Pb * g dw-1). However, since the correlationsbetween heavy metals and cellulose were not significantly different at the different sites, random sampling variation could not be ruled out as an explanation of the different results for the different sites. The causes of the correlationbetween organic matter quality and heavy metals have not yet been clarified. Analysis of mor samples incubated in thelaboratory for 2 yr with 1200 g Pb * g dw-1 or 5 gHg * g dw-1 did not show any differences in carbohydrate composition, compared to control samples. This shows that within-site studies of correlations between respiration rate and heavy metals have to be combined with studies of metal additions to soils and analysis of organic matter quality beforeany valid conclusions can be made. 相似文献