首页> 外文会议>International conference on environmental remediation and radioactive waste management;ICEM2010 >MACROPOROUS CATALYSTS FOR HYDROTHERMAL OXIDATION OF METALLORGANIC COMPLEXES AT LIQUID RADIOACTIVE WASTE TREATMENT
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MACROPOROUS CATALYSTS FOR HYDROTHERMAL OXIDATION OF METALLORGANIC COMPLEXES AT LIQUID RADIOACTIVE WASTE TREATMENT

机译:液态放射性废物处理过程中用于金属有机物水热氧化的宏观催化剂

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One of the main problems of liquid radioactive waste (LRW) management is concerned with treatment of decontamination waters containing organic ligands. The organic ligands like oxalic, citric and ethylenediaminetetraacetic acids form stable complexes with radionuclides which puts restrictions on application of many technologies of LRW management. One of the ways of destruction of metallorganic complexes consists in using the catalytic oxidation. However, the heterophase catalytic oxidation is rather problematic due to formation of metal oxides on the catalyst surface and calmatation of meso- and micropores. A possible solution of the above problem can be found in synthesis of macroporous catalysts for oxidation having a regular macroporous structure.The present paper describes the template synthesis of macroporous metalloxide catalysts performed with using siloxane-acrylate microemulsions as templates. The method for impregnation of precious metals (PM) particles into the template, which enables one to produce PM nanoparticles of a specific size and immobilize them in the porous structure of the synthesized metalloxide catalysts, is presented. A possible mechanism of the synthesis of macroporous catalysts is suggested and the comparison of the electronic and photon-correlation spectroscopy results obtained at different stages of catalysts synthesis was conducted.
机译:液体放射性废物(LRW)管理的主要问题之一是处理含有有机配体的去污水。草酸,柠檬酸和乙二胺四乙酸等有机配体与放射性核素形成稳定的络合物,这限制了LRW管理的许多技术的应用。破坏金属有机配合物的方法之一是使用催化氧化。然而,由于在催化剂表面上形成金属氧化物以及中孔和微孔的稳定化,异相催化氧化是相当成问题的。在具有规则大孔结构的用于氧化的大孔催化剂的合成中,可以找到上述问题的可能解决方案。 本文描述了以硅氧烷-丙烯酸酯微乳液为模板进行的大孔金属氧化物催化剂的模板合成。提出了将贵金属(PM)颗粒浸渍到模板中的方法,该方法使人们能够生产特定尺寸的PM纳米颗粒并将其固定在合成的金属氧化物催化剂的多孔结构中。提出了大孔催化剂合成的可能机理,并对催化剂合成不同阶段得到的电子和光子相关光谱结果进行了比较。

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