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The use of ultra filtration in trace metal speciation studies in sea water

机译:超滤技术在海水中痕量金属形态研究中的应用

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During this work, size fractionation technique "ultra filtration" is used in speciation studies of trace elements in the coastal sea water. Filtration is the most commonly used method to fractionate trace metal species, but often only "dissolved" and "particulate" fraction. The purpose of the present study is to determine colloidal and suspended particulate concentrations of Fe, Zn, Cu, Ni, and Mn in sea water. Suspended particulate matter were separated in three different size groups namely (>2.7 μm, <2.7->0.45 μm and < 0.45- >0.22 μm) by suction filtration using cellulose acetate and nitrate filter membranes. Thereafter to concentrate the solution with colloidal particle < 0.22 μm-1.1 nm (0.5 k Nominal Molecular Weight cut-off Limit {NMWL}), the solution obtained from filtration through < 0.22 μm, is sequentially passed through the ultra-filtration membranes having pore diameters of 14 nm (300 k NMWL), 3.1 nm (50 k NMWL), 2.2 nm (30 k NMWL), 1.6 nm (10 k NMWL) and 1.1 nm (0.5 k NMWL) by using Stirred Ultra-filtration Cells, operating in concentration mode. The concentration of Fe, Zn, Cu, Ni, and Mn were measured in suspended and dissolved fraction by ion chromatography, ICP-AES and Atomic Absorption Spectrometer. The salinity of the solution in various dissolved fractions of sequential filtration varies between 30.89-34.22 parts per thousand. The maximum concentrations of colloidal Zn, Cu, Ni and Mn in dissolved fraction were in < 2.2—> 1.6 nm fraction. In case of Fe, colloidal fractions < 2.2->1.6 nm and < 1.6-< 1.1 nm shows higher concentration. The concentration of Zn, Cu, Ni and Mn increase with decrease in size in suspended particulate matter, while the reverse is observed in case of Fe. This size separation data that specifies the partitioning of metals between dissolved and suspended solid phases is necessary for developing physically based models of metal transport in aquatic system.
机译:在这项工作中,尺寸分馏技术“超滤”被用于沿海海水中微量元素的形态研究。过滤是分离痕量金属种类最常用的方法,但通常仅是“溶解的”和“颗粒状”的馏分。本研究的目的是确定海水中Fe,Zn,Cu,Ni和Mn的胶体和悬浮颗粒浓度。通过使用醋酸纤维素和硝酸盐滤膜进行抽滤,将悬浮的颗粒物分为三个不同的尺寸组(> 2.7μm,<2.7-> 0.45μm和<0.45-> 0.22μm)。此后,为了浓缩胶体粒子<0.22μm-1.1nm(0.5 k标称分子量截断极限{NMWL})的溶液,将通过<0.22μm过滤获得的溶液依次通过具有孔的超滤膜使用搅拌式超滤池,操作的直径分别为14 nm(300 k NMWL),3.1 nm(50 k NMWL),2.2 nm(30 k NMWL),1.6 nm(10 k NMWL)和1.1 nm(0.5 k NMWL)在集中模式下。通过离子色谱,ICP-AES和原子吸收光谱仪测量悬浮和溶解部分中的Fe,Zn,Cu,Ni和Mn的浓度。依次过滤的各种溶解部分中溶液的盐度在千分之30.89-34.22之间变化。溶解级分中胶体Zn,Cu,Ni和Mn的最大浓度为<2.2-> 1.6 nm级分。对于Fe,胶体级分<2.2-> 1.6 nm和<1.6- <1.1 nm显示更高的浓度。 Zn,Cu,Ni和Mn的浓度随悬浮颗粒物尺寸的减小而增加,而Fe则相反。这种尺寸分离数据指定了溶解固相和悬浮固相之间金属的分配,这对于开发基于物理的水生系统金属迁移模型是必要的。

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