污泥中重金属的去除及回收试验

论述了利用离子交换技术循环使用柠檬酸去除污泥中重金属,并置换回收重金属的适宜工艺条件.经柠檬酸处理后,污泥中90%以上的重金属被去除;柠檬酸处理液中的重金属用离子交换法回收,考察了树脂种类、流速、操作方式等因素对离子交换、再生效果的影响;在适宜工艺条件下,重金属的交换率均为100%,而洗脱率均接近90%;柠檬酸及离子交换树脂循环使用,重金属也得到回收,降低了处理成本.     

河口近岸水体中颗粒态重金属的潮周期变化

对长江口崇明东滩近岸水体中颗粒态重金属的潮周期变化特征及其影响机制进行了研究.结果表明,受粒度影响,底层水体中颗粒态Cu、Pb、Fe、Mn、Zn、Cr、Al的总量分别高出表层沉积物的184%、99%、56%、62%、147%、50%和45%,其中Cu、Pb、Fe、Mn、Zn、Al可还原态部分在底层水体悬浮颗粒物中的含量也明显高出表层沉积物的2～3倍,但与重金属总量相比,上述元素的可还原态部分所占比例与表层沉积物相差不大.在5次潮汐循环过程中,颗粒态重金属均在涨潮初期、高平潮前后及落潮末期出现较高含量.这种变化主要与水动力条件有关,当水体流速增大时,从底部沉积物再悬浮起来的颗粒态重金属对水体中的永久性悬浮颗粒起了很大的稀释效应.水体中的盐度、DO及pH等环境因子对潮周期内颗粒态重金属的变化影响不大.     

The influence of metal source uncertainty on cost-effective allocation of mine water pollution abatement in catchments

In mine water pollution abatement, it is commonly assumed that known mine waste sites are the major pollution sources, thus neglecting the possibility of significant contribution from other old and diffuse sources within a catchment. We investigate the influence of different types of pollution source uncertainty on cost-effective allocation of abatement measures for mine water pollution. A catchment-scale cost-minimization model is developed and applied to the catchment of the river Dalälven, Sweden, in order to exemplify important effects of such source uncertainty. Results indicate that, if the pollution distribution between point and diffuse sources is partly unknown, downstream abatement measures, such as constructed wetlands, at given compliance boundaries are often cost-effective. If downstream abatement measures are not practically feasible, the pollution source distribution between point and diffuse mine water sources is critical for cost-effective solutions to abatement measure allocation in catchments. In contrast, cost-effective solutions are relatively insensitive to uncertainty in total pollutant discharge from mine water sources.     

Field reconnaissance and estimation of petroleum hydrocarbon and heavy metal contents of soils affected by the Ebocha-8 oil spillage in Niger Delta, Nigeria

Field reconnaissance of the Ebocha-8 oil spill-affected site at Obiobi/Obrikom in the Niger Delta region of Nigeria was carried out to assess the extent of damage to the terrestrial ecosystem and delimit the epicenter of oil spillage. Following three successive reconnaissance surveys, the area to be sampled was delimited (200 x 200 m2), and soil samples were collected using the grid method from three replicate quadrats at two depths, surface (0-15 cm) and subsurface (15-30 cm). A geographically similar area located 50 m adjacent to the oil-polluted area was used as a reference (control) site. Total hydrocarbon content (THC) and heavy metal concentrations were later determined in the laboratory by extraction and spetrophotemetric techniques. Generally, the THC of soils at surface and subsurface depths of the oil-polluted plots was 2.06 x 10(4) +/- 4.97 x 10(3) mg/kg and 1.67 x 10(3) +/- 3.61 x 10(2) mg/kg soil, respectively, (no overlap in standard errors at 95% confidence limit) while concentrations of heavy metals(Pb, Cd, V, Cu and Ni) were enhanced, especially at the surface. The high levels of THC and heavy metals may predispose the site, which hitherto served as arable agricultural land, to impaired fertility and possible conflagration. When concentrations of heavy metals reach the levels obtained in this study, they may become toxic to plants or possibly bio-accumulate, thus leading to toxic reactions along the food chain. While the spilled-oil may have contributed to the enhanced levels of the metals in the affected soils, physico-chemical properties of the soils, mobility of metals, and the intense rainfall and flooding that preceded the period of study may have also contributed in part to their enhanced concentrations. The presence of high hydrocarbon content may cause oxygen deprivation, which may result in the death of soil fauna by asphyxiation. There is, therefore, an urgent need to clear the affected site of these excess hydrocarbon deposits so as to enhance the rehabilitation process of the affected mat layer of soils. Other appropriate mitigating measures, such as subsequent monitoring of hydrocarbon levels at suitable intervals after the clean up activities, are also recommended, with reference to the findings of this study, for effective management of the affected area.     

薄膜扩散梯度技术在重金属生物有效态监测中的应用

重金属生物有效性是评估重金属元素迁移性、生物可利用性和生态影响的关键参数。薄膜扩散梯度技术(DGT)是一种原位被动采样技术,因其具有原位富集性、形态选择性,可提供被监测物质在监测时间段内的平均浓度等优点,可作为生物对重金属摄取的模拟替代物对环境介质中重金属的生物可利用度进行预测,已被广泛应用于环境介质中重金属生物有效性的测定。研究主要介绍了DGT技术的原理、组成和特点,评述了其近年来在水体、土壤、沉积物中重金属生物有效态应用方面的新进展,提出了DGT技术未来要提高抗生物污染能力及寻找可与DGT技术联用的相关技术的观点。     

长三角典型区土壤重金属有效态的协同区域化分析、空间相关分析与空间主成分分析

以昆山市为典型区,采集了126个表层土壤样品,通过多元统计学、地统计学与GIS技术相结合,采用基于协同区域化理论的因子克立格法探讨了长三角多个土壤重金属有效态的区域分异,并在剖析不同空间尺度有效态重金属的空间结构特征基础上,应用空间相关分析和空间主成分分析来揭示引起这种分布格局的成因和污染来源,结果表明,昆山土壤有效态重金属服从正态或对数正态分布,变异系数较大,有效态Cd污染最重.重金属有效态在空间上可划分为块金尺度、小空间尺度（15 km左右）和大空间尺度（40 km左右）,它可用3个尺度的实验（交叉）变异函数的协同区域化模型线性拟合.空间相关分析中,Cd和Zn在3个尺度中的相关性均极显著,且元素在小尺度和大尺度的相关性比块金尺度更强,大尺度的负相关特征较其它尺度明显.空间主成分分析表明,不同尺度的空间污染来源不同.重金属有效态第一、二主成分的空间分布格局结果表明重金属有效态含量与工业活动、污水灌溉和土壤性质密切相关.     

风浪扰动对太湖水体重金属形态的影响

对不同风浪条件下水体中的悬浮颗粒物,采用ICP-AES测定其中Co,Cr,Cu,Ni,Pb,Zn,Al,Fe和Mn不同形态的含量.研究表明,水体中Al,Fe,Co,Cr,Pb和Ni可提取态含量随风浪扰动程度的增强其含量均有不同程度的增大. Mn,Zn和Cu在7m·s-1风浪下含量最高,11m·s-1风浪次之,2m·s-1风浪最小.7m·s-1风浪与2m·s-1风浪相比,水体中Mn, Co, Cr, Zn, Cu和Ni的B1, B2, B3态含量增加3-20倍.11m·s-1风浪与7m·s-1风浪相比,Co, Cr和Ni的B1态含量分别增加31.1%-76.8%,Mn, Zn和Cu分别减少22.1%-38.6%; Cr,Zn和Ni的B2态含量增加12.1%-50.2%, Mn减少65.6%, Co和Cu的含量相当; Co和Ni的B3态含量增加15.4%-10.3%,Cr,Mn,Zn和Cu略微减少.水体中的金属主要以Fe-Mn氧化物结合态存在,且金属的三态比例随风浪的变化不明显. Mn的生物有效性最高,Zn,Cu和Ni次之,毒性较大的Pb和Cr的生物有效性较低.Al, Fe和Pb的Fe-Mn氧化物结合态比例非常高,约有74.56%-100%. Co,Cr和Ni的有机结合态比例较高,且Co和 Ni的三态比例比较均一,Cu的B3态较低.     

长江口潮滩沉积物中活性重金属的空间分异及控制机制

利用盐酸羟氨-25%醋酸溶液,提取了长江口潮滩沉积物中活性重金属含量。研究发现,长江口潮滩沉积物中活性重金属占总量的百分含量依次为Cu 26%,Pb 36%,Fe 7%,Mn 49%,Zn 32%,Cr 14%和Al 16%,沉积物基本未受到Cr污染,其余重金属污染程度处于中等偏下水平。除Zn、Cr外,其余活性重金属在夏季沉积物中的含量明显低于春季,其主要原因是夏季风暴潮将大量细颗粒泥沙及其富集的重金属带离潮滩进入了河口水体中。受点源污染排放及沉积物粒度影响,活性重金属在长江口南岸的浒浦、顾路和浦东机场出现峰值含量,且高潮滩含量明显高于中、低潮滩。在垂向上,重金属一般在沉积物表层或亚表层形成富集。在口门附近的滨岸潮滩沉积物中,Cu、Pb的空间分异主要受早期成岩作用的控制,在污染较为严重、水动力作用相对较弱的潮滩沉积物中,Cu、Pb的空间分异主要受沉积物中有机质含量变化的控制.     

The Response of Hydrophytes to Environmental Pollution with Heavy Metals

The effects of Cu²⁺, Cd²⁺, and Ni²⁺ at low and high concentrations (0.025 and 0.25 mg/ml) on the accumulation capacity, the state of the pigment complex, and photosynthesis rate have been studied in model experiments with three floating hydrophytes (Hydrocharis morsus-ranae L., Lemna gibba L., and Potamogeton natans L.) and four submerged hydrophytes (Elodea canadensis Michx., Lemna trisulka L., Ceratophyllum demersum L., and Potamogeton lucens L.). Copper and cadmium are especially toxic at the concentrations studied. The effect of Cu²⁺ was the strongest in hydatophytes, and the effect of Cd²⁺, in pleustophytes. It is hypothesized that the differences between hydrophytes with respect to accumulation of metals and decrease in photosynthesis rate may cause predominant elimination of submerged species. Therefore, changes in the species structure of hydrophyte communities may be expected in waters polluted with metals.     

Statistical comparison and correlation of zinc and lead in estuarine sediments along the western coast of Mauritius

Cr, Zn and Pb were quantified using atomic absorption spectrometry (AAS) from urban and rural estuarine sediments collected along the western coast of Mauritius during the period July 2002-January 2003. The mean concentration of Cr (225.4 mg kg(-1)), Zn (107.0 mg kg(-1)) and Pb (27.0 mg kg(-1)) in sediments along the six estuaries can be considered below those from contaminated estuarine sediments. Zn and Pb were significantly higher in urban sediments downstream St. Louis River compared to a rural estuary at Tamarin at 5% significance level. Zn was also significantly lower in Tamarin compared to Petite Riviere Noire estuary. Cr was however not significantly different in sediments from the six estuaries and could be considered of basaltic origin and were correlated to neither lead nor zinc. The concentration of Zn and Pb were greatest in the more urbanised upper and lower reaches of the St. Louis estuary during the period of study and were also significantly positively correlated in the estuarine sediments indicating that the cycling of Pb and Zn were linked indicating a common source for Pb and Zn. The potential sources of Pb and Zn in the urban estuarine sediments were considered to arise from road runoff causing significant quantities to be trapped. At present, compared to contaminant levels found in the UK and elsewhere, Mauritius still looks relatively uncontaminated but there is growing concern about heavy metal contamination in urban estuaries. There is therefore a need for long-term studies in estuarine management to involve integrated strategies in which water-sediment interactions in estuaries need to be considered and international standards for sediment quality developed. Such studies undertaken in the future would further the understanding of the biogeochemical processes of estuarine systems in Mauritius which could then be used in environmental development schemes and effective coastal zone management.