{"title":"MX-80在结晶岩Ca-Na-Cl型基准水中对Np(IV)的吸附","authors":"S. Nagasaki","doi":"10.7733/JNFCWT.2021.19.1.1","DOIUrl":null,"url":null,"abstract":"This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/ by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited The pH dependence of sorption distribution coefficient (Kd) of Np(IV) on MX-80 in Ca-Na-Cl type solution with the ionic strength of 0.3 M, which was similar to one of the reference groundwaters in crystalline rock, was experimentally investigated under the reducing conditions. The overall trend of Kd on MX-80 was independent of pH at 5 ≤ pH ≤ 10 but increased as pH increased at pH ≤ 5. The 2-site protolysis non-electrostatic surface complexation and cation exchange model was applied to the experimentally measured pH dependence of Kd and the optimized surface complexation constants of Np(IV) sorption on MX-80 were estimated. The values of surface complexation constants in this work agreed relatively well with those in the Na-Ca-Cl solution previously evaluated, suggesting that compared to Na+, the competition of Ca2+ with Np(IV) for surface complexation on MX-80 was not much strong in Ca-Na-Cl solution. The sorption model well predicted the pH dependence of Kd values but slightly overestimated the sorption at the low pH region.","PeriodicalId":17456,"journal":{"name":"Journal of the Nuclear Fuel Cycle and Waste Technology","volume":"98 1","pages":"1-7"},"PeriodicalIF":0.0000,"publicationDate":"2021-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sorption of Np(IV) on MX-80 in Ca-Na-Cl Type Reference Water of Crystalline Rock\",\"authors\":\"S. Nagasaki\",\"doi\":\"10.7733/JNFCWT.2021.19.1.1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/ by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited The pH dependence of sorption distribution coefficient (Kd) of Np(IV) on MX-80 in Ca-Na-Cl type solution with the ionic strength of 0.3 M, which was similar to one of the reference groundwaters in crystalline rock, was experimentally investigated under the reducing conditions. The overall trend of Kd on MX-80 was independent of pH at 5 ≤ pH ≤ 10 but increased as pH increased at pH ≤ 5. The 2-site protolysis non-electrostatic surface complexation and cation exchange model was applied to the experimentally measured pH dependence of Kd and the optimized surface complexation constants of Np(IV) sorption on MX-80 were estimated. The values of surface complexation constants in this work agreed relatively well with those in the Na-Ca-Cl solution previously evaluated, suggesting that compared to Na+, the competition of Ca2+ with Np(IV) for surface complexation on MX-80 was not much strong in Ca-Na-Cl solution. The sorption model well predicted the pH dependence of Kd values but slightly overestimated the sorption at the low pH region.\",\"PeriodicalId\":17456,\"journal\":{\"name\":\"Journal of the Nuclear Fuel Cycle and Waste Technology\",\"volume\":\"98 1\",\"pages\":\"1-7\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-03-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the Nuclear Fuel Cycle and Waste Technology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.7733/JNFCWT.2021.19.1.1\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Nuclear Fuel Cycle and Waste Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7733/JNFCWT.2021.19.1.1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
这是一篇基于知识共享归属非商业许可(http://creativecommons.org/licenses/ by-nc/3.0)的开放获取文章,该许可允许在任何媒介上不受限制地进行非商业使用、分发和复制,前提是正确引用原始作品。在离子强度为0.3 M的Ca-Na-Cl型溶液中,Np(IV)对MX-80的吸附分布系数(Kd)的pH依赖性。与结晶岩中的一种参考地下水相似,在还原条件下进行了实验研究。在5≤pH≤10时,MX-80上Kd的总体变化趋势与pH无关,但在pH≤5时,Kd随pH的增大而增大。将2位元解非静电表面络合和阳离子交换模型应用于实验测量Kd对pH的依赖,并估计了MX-80吸附Np(IV)的最佳表面络合常数。本文计算的表面络合常数值与前人评价的Na- ca - cl溶液中的表面络合常数值吻合较好,表明与Na+相比,Ca-Na-Cl溶液中Ca2+与Np(IV)对MX-80表面络合的竞争并不强。该吸附模型较好地预测了Kd值对pH的依赖关系,但对低pH区吸附的估计略高。
Sorption of Np(IV) on MX-80 in Ca-Na-Cl Type Reference Water of Crystalline Rock
This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/ by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited The pH dependence of sorption distribution coefficient (Kd) of Np(IV) on MX-80 in Ca-Na-Cl type solution with the ionic strength of 0.3 M, which was similar to one of the reference groundwaters in crystalline rock, was experimentally investigated under the reducing conditions. The overall trend of Kd on MX-80 was independent of pH at 5 ≤ pH ≤ 10 but increased as pH increased at pH ≤ 5. The 2-site protolysis non-electrostatic surface complexation and cation exchange model was applied to the experimentally measured pH dependence of Kd and the optimized surface complexation constants of Np(IV) sorption on MX-80 were estimated. The values of surface complexation constants in this work agreed relatively well with those in the Na-Ca-Cl solution previously evaluated, suggesting that compared to Na+, the competition of Ca2+ with Np(IV) for surface complexation on MX-80 was not much strong in Ca-Na-Cl solution. The sorption model well predicted the pH dependence of Kd values but slightly overestimated the sorption at the low pH region.