Suppr超能文献

具有限制亚铁离子的赤铁矿的面依赖性 U(VI)去除。

Facet-dependent U(VI) removal of hematite with confined ferrous ions.

机构信息

College of Environmental Science and Engineering, North China Electric Power University, Beijing, 102206, People's Republic of China.

Key Laboratory of Comprehensive and Highly Efficient Utilization of Salt Lake Resources, Qinghai Province Key Laboratory of Resources and Chemistry of Salt Lakes, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining, Qinghai, 810008, People's Republic of China.

出版信息

Environ Sci Pollut Res Int. 2023 Oct;30(50):109077-109086. doi: 10.1007/s11356-023-30044-3. Epub 2023 Sep 28.

Abstract

The presence of ferrous minerals has been demonstrated to have a significant impact on the destiny, migration, and availability of uranyl (U(VI)) in natural surroundings. The iron oxide/Fe(II) system is a multifaceted iron reduction system anchored to surfaces, encompassing various forms of iron and ferrous ions. Several studies have investigated the effectiveness of adsorbed ferrous iron on iron-based minerals to facilitate the reduction of heavy metal ions and radioactive nuclides. A range of techniques for characterization, including X-ray photoelectron spectroscopy (XPS) and Mössbauer spectroscopy, were employed to explore the process of U(VI) adsorption and deposition, focusing on the limited region containing ferrous iron on the exposed crystalline surface of hematite. In this specific investigation, two kinds of hematite nanocrystals primarily exposing {001} and {012} crystal facets, referred to as HNPs and HNCs, were synthesized. Their ability to remove U(VI) was examined. Ferrous ions (Fe(II)) adsorbed onto the surface of hematite nanocrystals significantly enhanced the efficiency of U(VI) remediation. Furthermore, the HNCs/Fe(II) system showed better U(VI) reduction ability than the HNPs/Fe(II) system. Remarkably, HNCs produced and consumed more electrons and hydroxyl radicals, indicating a more intense response. This finding serves to highlight the significance of their role in interfacial effects and in predicting the spatial distribution of U(VI) in aqueous systems.

摘要

亚铁矿物的存在被证明对铀酰(U(VI))在自然环境中的归宿、迁移和可用性具有重大影响。氧化铁/Fe(II)体系是一种多相铁还原体系,以表面为锚点,包含各种形式的铁和亚铁离子。已有多项研究探讨了吸附亚铁铁在铁基矿物上促进重金属离子和放射性核素还原的有效性。一系列的表征技术,包括 X 射线光电子能谱(XPS)和穆斯堡尔光谱,被用于研究 U(VI)的吸附和沉积过程,重点关注暴露的赤铁矿晶面上有限区域内的亚铁铁。在这项具体研究中,合成了两种主要暴露{001}和{012}晶面的赤铁矿纳米晶体,分别称为 HNPs 和 HNCs,并考察了它们去除 U(VI)的能力。吸附在赤铁矿纳米晶体表面的亚铁离子(Fe(II))显著提高了 U(VI)修复的效率。此外,HNCs/Fe(II)体系比 HNPs/Fe(II)体系具有更好的 U(VI)还原能力。值得注意的是,HNCs 产生和消耗了更多的电子和羟基自由基,表明反应更剧烈。这一发现突出了它们在界面效应中的作用以及在预测水相体系中 U(VI)空间分布方面的重要性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验