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Application of structural analogs of dimercaptosuccinic acid-functionalized silica nanoparticles (DMSA-[silica]) to adsorption of mercury, cadmium, and lead

机译:二巯基琥珀酸官能化的二氧化硅纳米粒子(DMSA- [silica])的结构类似物在汞,镉和铅的吸附中的应用

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In order to gain additional insight into mercury selectivity with nano-sized DMSA-[silica], we investigated a series of ligands related to DMSA, these are: monomercaptosuccinic acid; MMSA, 2-mercapto-4-methyl-5-thiazoleacetic acid; MCT, ortho-thiosalicylic acid; o-TSA and para-thiosalicylic acid; p-TSA. The MMSA chelate is structurally similar to DMSA except that it has only one thiol group. The chelates o-TSA and p-TSA each have one thiol and one carboxylic acid group. MCT includes neutral S and N atoms in close proximity to the thiolate binding site. MCT, o-TSA and p-TSA resemble each other in having equal numbers of carboxylic acid and thiol groups and formation of amide bonds with the linker on silica is expected to eliminate the carboxylate binding sites, making thiolates the only binding sites for Hg(II), Cd(II), and Pb(II) metals ions in the nano-sized; MMSA-[silica], MCT-[silica], o-TSA-[silica], and p-TSA-[silica]. Each of the nano-sized MMSA-[silica], MCT-[silica], o-TSA-[silica], and p-TSA-[silica], show a higher preference for Hg(II) over Cd(II) and Pb(II) compared to the same free chelates in solution, respectively. In addition, there are differences in the level of metal ion chelation for each functionalized silica nanoparticle. These differences in the degree of metal chelation for each functionalized silica nanoparticles surface are explained by the difference in thiolate/carboxylate ratio upon attachment to the surface and on steric reasons based on the orientation of the thiol groups on the surface. When attached via amide bond formation, the thiolate site in o-TSA-[silica] will face towards the silica surface, while for p-TSA-[silica], the thiolate site is expected to be pointed outwards and away from the silica surface. In comparing MMSA-[silica] to DMSA-[silica], the thiolate/carboxylate ratio decreases from 2/1 in DMSA-[silica] to 1/1 in MMSA-[silica] (assuming attachment via one amide bond in each case). This effect of increasing the ratio of thiolate to carboxylate upon attachment to the surface is believed to play a role in the selectivity enhancement towards Hg(II) over Cd(II) and Pb(II).
机译:为了进一步了解纳米级DMSA- [SiO2]对汞的选择性,我们研究了与DMSA相关的一系列配体,它们是:单体巯基琥珀酸; MMSA,2-巯基-4-甲基-5-噻唑乙酸; MCT,原硫代水杨酸; o-TSA和对硫代水杨酸; p-TSA。 MMSA螯合物在结构上与DMSA类似,不同之处在于它仅具有一个巯基。螯合剂o-TSA和p-TSA各自具有一个硫醇和一个羧酸基团。 MCT包含紧邻硫醇盐结合位点的中性S和N原子。 MCT,o-TSA和p-TSA彼此相似,具有相同数量的羧酸和硫醇基团,并且与二氧化硅上的连接基形成酰胺键有望消除羧酸盐的结合位点,从而使硫醇盐成为汞的唯一结合位点( II),Cd(II)和Pb(II)纳米离子; MMSA- [二氧化硅],MCT- [二氧化硅],o-TSA- [二氧化硅]和p-TSA- [二氧化硅]。纳米级MMSA- [二氧化硅],MCT- [二氧化硅],o-TSA- [二氧化硅]和p-TSA- [二氧化硅]相对于Cd(II)和Cd(II)具有更高的Hg(II)偏爱性。 Pb(II)分别与溶液中的相同游离螯合物相比。另外,每种官能化的二氧化硅纳米颗粒的金属离子螯合水平存在差异。每个官能化的二氧化硅纳米粒子表面的金属螯合度的这些差异可通过附着在表面上的硫醇盐/羧酸盐比率的差异以及基于表面上硫醇基团的取向的空间原因来解释。当通过酰胺键形成连接时,o-TSA- [二氧化硅]中的硫醇盐位点将面对二氧化硅表面,而对于p-TSA- [二氧化硅],该硫醇盐位点应指向外部并远离二氧化硅表面。在将MMSA- [二氧化硅]与DMSA- [二氧化硅]进行比较时,硫醇盐/羧酸盐的比例从DMSA- [二氧化硅]中的2/1降低到MMSA- [二氧化硅]中的1/1(假设在每种情况下均通过一个酰胺键连接) )。据信,增加附着在表面上的硫醇盐与羧酸盐的比例的这种作用在对Cg(II)和Pb(II)的Hg(II)选择性增强中起作用。

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