Naylor C, Davison W, Motelica-Heino M, Van Den Berg G A, Van Der Heijdt L M
IENS, ES, Lancaster University, Lancaster LA1 4YQ, UK.
Sci Total Environ. 2004 Jul 26;328(1-3):275-86. doi: 10.1016/j.scitotenv.2004.02.008.
The technique of DGT (Diffusive Gradients in Thin Films) was further developed to allow simultaneous measurement of sulfide and trace metals at the same location in sediment. The new combined DGT probe consisted of a layer of gel impregnated with AgI, overlain by (1) a layer of gel containing Chelex, (2) a layer of gel and (3) a filter membrane. Diffusion of sulfide was controlled by layers (1) to (3), while diffusion of metals was controlled by layers (2) and (3). The Chelex gel trapped metals that were measured after elution with acid. The AgI gel trapped sulfide through the formation of Ag2S. This was then measured densitometrically as the colour changed from pale yellow to grey. Experiments demonstrated that concentrations of metal or sulfide measured by the combined device were no different to the concentrations measured by more conventional devices. The presence of Chelex in the gel did not impede the diffusion of sulfide. Deployment of a combined probe in marine sediment revealed simultaneous remobilisation of metals and sulfide at the same location. Solubility calculations indicated that some precipitation of amorphous FeS was probably occurring at the maxima in sulfide concentrations. There was general undersaturation with respect to NiS, but ZnS was supersaturated at all locations. There appeared to be localised active zones of organic matter decomposition, where reduction of manganese oxides, iron oxides and sulfate occurred simultaneously. Mass balance calculations indicated that Ni could not be supplied by release from decomposing organic matter. Manganese oxides were the most likely source, but supply from reductive dissolution of iron oxides could not be entirely discounted. Supply from either Fe or Mn oxides could account for the Zn maxima. Application of the newly developed combined probe provides new information that helps understanding of the complex nature of trace metal and sulfur chemistry in sediments.
薄膜扩散梯度(DGT)技术得到了进一步发展,以实现对沉积物中同一位置的硫化物和痕量金属的同步测量。新型组合式DGT探针由一层浸渍有碘化银的凝胶组成,上面覆盖着:(1)一层含有螯合树脂的凝胶;(2)一层凝胶;(3)一层滤膜。硫化物的扩散由(1)至(3)层控制,而金属的扩散由(2)和(3)层控制。螯合树脂凝胶捕获金属,在用酸洗脱后进行测量。碘化银凝胶通过形成硫化银捕获硫化物。然后随着颜色从浅黄色变为灰色,通过密度测定法对其进行测量。实验表明,组合装置测量的金属或硫化物浓度与更传统装置测量的浓度没有差异。凝胶中螯合树脂的存在并不妨碍硫化物的扩散。在海洋沉积物中部署组合探针揭示了在同一位置金属和硫化物的同步再活化。溶解度计算表明,在硫化物浓度最大值处可能发生了一些非晶态硫化铁的沉淀。相对于硫化镍普遍不饱和,但硫化锌在所有位置都过饱和。似乎存在局部的有机物分解活跃区,在那里同时发生了氧化锰、氧化铁和硫酸盐的还原。质量平衡计算表明,镍不可能由分解的有机物释放提供。氧化锰是最可能的来源,但氧化铁还原溶解的供应也不能完全排除。铁或锰氧化物的供应都可以解释锌的最大值。新开发的组合探针的应用提供了有助于理解沉积物中痕量金属和硫化学复杂性质的新信息。