Ji Hoon Lee , Jinseok Kim , Jang-Soon Kwon , Ho Young Jo
{"title":"不同ph值富钾溶液中ca -膨润土水热蚀变对其理化、溶胀及Cs吸附性能的影响","authors":"Ji Hoon Lee , Jinseok Kim , Jang-Soon Kwon , Ho Young Jo","doi":"10.1016/j.apgeochem.2023.105791","DOIUrl":null,"url":null,"abstract":"<div><p><span>Understanding the stability of the bentonite buffer when exposed to cement leachates at temperatures exceeding 100°C is crucial for optimizing the design of deep geological repositories (DGRs) for high-level </span>radioactive wastes<span> (HLRWs) and minimizing the required site area. Experiments were conducted under hydrothermal conditions at 150°C for 30–150 days using deionized (DI) water (pH 6) and K-rich solutions (1 mol/L KCl, pH 6 and 1 mol/L KOH, pH 13) on Ca-bentonite. The 1 mol K concentration is comparable to 15 times the cation exchange capacity (CEC) of raw bentonite. Using various analytical techniques, the mineralogical, physicochemical, swelling, and Cs<span> adsorption characteristics of raw and reacted bentonite samples were determined. Almost no changes in the properties of bentonite reacted with DI water were found for a given reaction time. For bentonite reacted with a 1 mol/L KCl solution, the cation exchange of Ca by K was a primary alteration process, resulting in a slight decrease in swelling capacity. However, almost no mineralogical changes were observed and consequently, there was minimal change in the Cs adsorption capacity. In contrast, for the bentonite reacted with a 1 mol/L KOH solution, the dominant alteration process was the transformation of minerals in bentonite into zeolite minerals, which resulted in significant changes in physicochemical properties, in particular, a decrease in the swelling capacity. On the other hand, the Cs adsorption capacity increased up to 2 times compared with the raw bentonite.</span></span></p></div>","PeriodicalId":8064,"journal":{"name":"Applied Geochemistry","volume":"158 ","pages":"Article 105791"},"PeriodicalIF":3.1000,"publicationDate":"2023-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effect of hydrothermal alteration of Ca-bentonite in K-rich solutions with different pHs on the physicochemical, swelling, and Cs adsorption properties\",\"authors\":\"Ji Hoon Lee , Jinseok Kim , Jang-Soon Kwon , Ho Young Jo\",\"doi\":\"10.1016/j.apgeochem.2023.105791\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>Understanding the stability of the bentonite buffer when exposed to cement leachates at temperatures exceeding 100°C is crucial for optimizing the design of deep geological repositories (DGRs) for high-level </span>radioactive wastes<span> (HLRWs) and minimizing the required site area. Experiments were conducted under hydrothermal conditions at 150°C for 30–150 days using deionized (DI) water (pH 6) and K-rich solutions (1 mol/L KCl, pH 6 and 1 mol/L KOH, pH 13) on Ca-bentonite. The 1 mol K concentration is comparable to 15 times the cation exchange capacity (CEC) of raw bentonite. Using various analytical techniques, the mineralogical, physicochemical, swelling, and Cs<span> adsorption characteristics of raw and reacted bentonite samples were determined. Almost no changes in the properties of bentonite reacted with DI water were found for a given reaction time. For bentonite reacted with a 1 mol/L KCl solution, the cation exchange of Ca by K was a primary alteration process, resulting in a slight decrease in swelling capacity. However, almost no mineralogical changes were observed and consequently, there was minimal change in the Cs adsorption capacity. In contrast, for the bentonite reacted with a 1 mol/L KOH solution, the dominant alteration process was the transformation of minerals in bentonite into zeolite minerals, which resulted in significant changes in physicochemical properties, in particular, a decrease in the swelling capacity. On the other hand, the Cs adsorption capacity increased up to 2 times compared with the raw bentonite.</span></span></p></div>\",\"PeriodicalId\":8064,\"journal\":{\"name\":\"Applied Geochemistry\",\"volume\":\"158 \",\"pages\":\"Article 105791\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2023-09-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied Geochemistry\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0883292723002366\",\"RegionNum\":3,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"GEOCHEMISTRY & GEOPHYSICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Geochemistry","FirstCategoryId":"89","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0883292723002366","RegionNum":3,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GEOCHEMISTRY & GEOPHYSICS","Score":null,"Total":0}
Effect of hydrothermal alteration of Ca-bentonite in K-rich solutions with different pHs on the physicochemical, swelling, and Cs adsorption properties
Understanding the stability of the bentonite buffer when exposed to cement leachates at temperatures exceeding 100°C is crucial for optimizing the design of deep geological repositories (DGRs) for high-level radioactive wastes (HLRWs) and minimizing the required site area. Experiments were conducted under hydrothermal conditions at 150°C for 30–150 days using deionized (DI) water (pH 6) and K-rich solutions (1 mol/L KCl, pH 6 and 1 mol/L KOH, pH 13) on Ca-bentonite. The 1 mol K concentration is comparable to 15 times the cation exchange capacity (CEC) of raw bentonite. Using various analytical techniques, the mineralogical, physicochemical, swelling, and Cs adsorption characteristics of raw and reacted bentonite samples were determined. Almost no changes in the properties of bentonite reacted with DI water were found for a given reaction time. For bentonite reacted with a 1 mol/L KCl solution, the cation exchange of Ca by K was a primary alteration process, resulting in a slight decrease in swelling capacity. However, almost no mineralogical changes were observed and consequently, there was minimal change in the Cs adsorption capacity. In contrast, for the bentonite reacted with a 1 mol/L KOH solution, the dominant alteration process was the transformation of minerals in bentonite into zeolite minerals, which resulted in significant changes in physicochemical properties, in particular, a decrease in the swelling capacity. On the other hand, the Cs adsorption capacity increased up to 2 times compared with the raw bentonite.
期刊介绍:
Applied Geochemistry is an international journal devoted to publication of original research papers, rapid research communications and selected review papers in geochemistry and urban geochemistry which have some practical application to an aspect of human endeavour, such as the preservation of the environment, health, waste disposal and the search for resources. Papers on applications of inorganic, organic and isotope geochemistry and geochemical processes are therefore welcome provided they meet the main criterion. Spatial and temporal monitoring case studies are only of interest to our international readership if they present new ideas of broad application.
Topics covered include: (1) Environmental geochemistry (including natural and anthropogenic aspects, and protection and remediation strategies); (2) Hydrogeochemistry (surface and groundwater); (3) Medical (urban) geochemistry; (4) The search for energy resources (in particular unconventional oil and gas or emerging metal resources); (5) Energy exploitation (in particular geothermal energy and CCS); (6) Upgrading of energy and mineral resources where there is a direct geochemical application; and (7) Waste disposal, including nuclear waste disposal.