• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

细菌还原铀的工程与动力学研究及其在铀污染环境修复中的应用。

Engineering and kinetic aspects of bacterial uranium reduction for the remediation of uranium contaminated environments.

机构信息

Tampere University, Faculty of Engineering and Natural Sciences, P.O. Box 541, FI- 33104, Tampere University, Finland; CSIRO Land and Water, 147 Underwood Avenue, Floreat, Western Australia, 6014, Australia.

CSIRO Land and Water, 147 Underwood Avenue, Floreat, Western Australia, 6014, Australia.

出版信息

J Hazard Mater. 2019 Jun 5;371:198-212. doi: 10.1016/j.jhazmat.2019.02.074. Epub 2019 Feb 21.

DOI:10.1016/j.jhazmat.2019.02.074
PMID:30851673
Abstract

Biological reduction of soluble uranium from U(VI) to insoluble U(IV) coupled to the oxidation of an electron donor (hydrogen or organic compounds) is a potentially cost-efficient way to reduce the U concentrations in contaminated waters to below regulatory limits. A variety of microorganisms originating from both U contaminated and non-contaminated environments have demonstrated U(VI) reduction capacity under anaerobic conditions. Bioreduction of U(VI) is considered especially promising for in situ remediation, where the activity of indigenous microorganisms is stimulated by supplying a suitable electron donor to the subsurface to contain U contamination to a specific location in a sparingly soluble form. Less studied microbial biofilm-based bioreactors and bioelectrochemical systems have also shown potential for efficient U(VI) reduction to remove U from contaminated water streams. This review compares the advantages and challenges of U(VI)-reducing in situ remediation processes, bioreactors and bioelectrochemical systems. In addition, the current knowledge of U(VI) bioreduction mechanisms and factors affecting U(VI) reduction kinetics (e.g. pH, temperature, and the chemical composition of the contaminated water) are discussed, as both of these aspects are important in designing efficient remediation processes.

摘要

从 U(VI)到不溶性 U(IV)的可溶性铀的生物还原与电子供体(氢或有机化合物)的氧化相结合,是一种将受污染水中的 U 浓度降低到监管限值以下的潜在经济有效的方法。来自受 U 污染和未受污染环境的各种微生物已证明在厌氧条件下具有 U(VI)还原能力。U(VI)的生物还原被认为特别适合原位修复,其中通过向地下供应合适的电子供体来刺激土著微生物的活性,将 U 污染以一种难溶的形式限制在特定位置。基于微生物生物膜的生物反应器和生物电化学系统的研究较少,但也显示出了从受污染水流中有效去除 U 的潜力。本文综述了 U(VI)还原原位修复过程、生物反应器和生物电化学系统的优缺点。此外,还讨论了影响 U(VI)还原动力学的 U(VI)生物还原机制和因素(例如 pH 值、温度和受污染水的化学成分),因为这两个方面在设计高效修复过程中都很重要。

相似文献

1
Engineering and kinetic aspects of bacterial uranium reduction for the remediation of uranium contaminated environments.细菌还原铀的工程与动力学研究及其在铀污染环境修复中的应用。
J Hazard Mater. 2019 Jun 5;371:198-212. doi: 10.1016/j.jhazmat.2019.02.074. Epub 2019 Feb 21.
2
Bioreduction of uranium in a contaminated soil column.污染土壤柱中铀的生物还原作用。
Environ Sci Technol. 2005 Jul 1;39(13):4841-7. doi: 10.1021/es050011y.
3
Optimization of a bioremediation system of soluble uranium based on the biostimulation of an indigenous bacterial community.基于对本地细菌群落进行生物刺激的可溶性铀生物修复系统的优化
Environ Sci Pollut Res Int. 2015 Jun;22(11):8442-50. doi: 10.1007/s11356-014-3980-7. Epub 2014 Dec 30.
4
Remediation and recovery of uranium from contaminated subsurface environments with electrodes.利用电极从受污染的地下环境中修复和回收铀。
Environ Sci Technol. 2005 Nov 15;39(22):8943-7. doi: 10.1021/es050457e.
5
Enhanced indigenous consortia for the remediation of uranium-contaminated groundwater by bioaugmentation: Reducing and phosphate-solubilizing consortia.通过生物强化修复铀污染地下水的强化本土菌群:还原菌群和溶磷菌群。
Sci Total Environ. 2024 Feb 20;912:168954. doi: 10.1016/j.scitotenv.2023.168954. Epub 2023 Nov 30.
6
Multiple influences of nitrate on uranium solubility during bioremediation of uranium-contaminated subsurface sediments.在铀污染的地下沉积物生物修复过程中硝酸盐对铀溶解度的多重影响
Environ Microbiol. 2002 Sep;4(9):510-6. doi: 10.1046/j.1462-2920.2002.00317.x.
7
Influences of organic carbon supply rate on uranium bioreduction in initially oxidizing, contaminated sediment.有机碳供应速率对初始氧化的污染沉积物中铀生物还原的影响。
Environ Sci Technol. 2008 Dec 1;42(23):8901-7. doi: 10.1021/es8019947.
8
Can microbially-generated hydrogen sulfide account for the rates of U(VI) reduction by a sulfate-reducing bacterium?微生物产生的硫化氢能否解释硫酸盐还原菌还原 U(VI)的速率?
Biodegradation. 2010 Feb;21(1):81-95. doi: 10.1007/s10532-009-9283-x. Epub 2009 Jul 14.
9
In situ bioreduction of uranium (VI) to submicromolar levels and reoxidation by dissolved oxygen.铀(VI)在原位生物还原至亚微摩尔水平并被溶解氧再氧化。
Environ Sci Technol. 2007 Aug 15;41(16):5716-23. doi: 10.1021/es062657b.
10
Bioreduction of U(VI) and stability of immobilized uranium under suboxic conditions.缺氧条件下U(VI)的生物还原及固定化铀的稳定性
J Environ Radioact. 2016 Apr;154:60-7. doi: 10.1016/j.jenvrad.2016.01.020. Epub 2016 Feb 6.

引用本文的文献

1
Uranium contamination mediating soil and ore microbial community assembly at four mining sites, South China.铀污染对中国南方四个矿区土壤和矿石微生物群落组装的影响
Front Microbiol. 2025 Feb 19;16:1553072. doi: 10.3389/fmicb.2025.1553072. eCollection 2025.
2
sp. strain MRS-1: A potential candidate for uranyl biosorption from uranyl polluted sites.菌株MRS-1:从铀污染场地生物吸附铀酰的潜在候选菌株。
Saudi J Biol Sci. 2023 Dec;30(12):103873. doi: 10.1016/j.sjbs.2023.103873. Epub 2023 Nov 11.
3
U mobilization and associated U isotope fractionation by sulfur-oxidizing bacteria.
硫氧化细菌介导的铀迁移及相关铀同位素分馏
Front Microbiol. 2023 Jul 18;14:1190962. doi: 10.3389/fmicb.2023.1190962. eCollection 2023.
4
Optimization of Environmental Conditions for Microbial Stabilization of Uranium Tailings, and the Microbial Community Response.铀尾矿微生物稳定化环境条件的优化及微生物群落响应
Front Microbiol. 2021 Dec 13;12:770206. doi: 10.3389/fmicb.2021.770206. eCollection 2021.
5
Application Progress of in Biological Treatment of Radioactive Uranium-Containing Wastewater.[此处原文不完整,缺少具体内容]在放射性含铀废水生物处理中的应用进展
Indian J Microbiol. 2021 Dec;61(4):417-426. doi: 10.1007/s12088-021-00969-9. Epub 2021 Aug 12.