Biogeochemistry of Actinides: Recent Progress and Perspective

IF 6.7 Q1 ENGINEERING, ENVIRONMENTAL ACS Environmental Au Pub Date : 2024-11-04 DOI:10.1021/acsenvironau.4c0003710.1021/acsenvironau.4c00037
Gauthier J.-P. Deblonde*, 
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Abstract

Actinides are elements that are often feared because of their radioactive nature and potentially devastating consequences to humans and the environment if not managed properly. As such, their chemical interactions with the biosphere and geochemical environment, i.e., their “biogeochemistry,” must be studied and understood in detail. In this Review, a summary of the past discoveries and recent advances in the field of actinide biogeochemistry is provided with a particular emphasis on actinides other than thorium and uranium (i.e., actinium, neptunium, plutonium, americium, curium, berkelium, and californium) as they originate from anthropogenic activities and can be mobile in the environment. The nuclear properties of actinide isotopes found in the environment and used in research are reviewed with historical context. Then, the coordination chemistry properties of actinide ions are contrasted with those of common metal ions naturally present in the environment. The typical chelators that can impact the biogeochemistry of actinides are then reviewed. Then, the role of metalloproteins in the biogeochemistry of actinides is put into perspective since recent advances in the field may have ramifications in radiochemistry and for the long-term management of nuclear waste. Metalloproteins are ubiquitous ligands in nature but, as discussed in this Review, they have largely been overlooked for actinide chemistry, especially when compared to traditional environmental chelators. Without discounting the importance of abundant and natural actinide ions (i.e., Th4+ and UO22+), the main focus of this review is on trivalent actinides because of their prevalence in the fields of nuclear fuel cycles, radioactive waste management, heavy element research, and, more recently, nuclear medicine. Additionally, trivalent actinides share chemical similarities with the rare earth elements, and recent breakthroughs in the field of lanthanide-binding chelators may spill into the field of actinide biogeochemistry, as discussed hereafter.

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锕系元素的生物地球化学:最新进展与展望
锕系元素因其放射性和如果管理不当可能对人类和环境造成的破坏性后果而常常令人恐惧。因此,必须详细研究和了解它们与生物圈和地球化学环境之间的化学相互作用,即它们的 "生物地球化学"。本综述概述了锕系元素生物地球化学领域过去的发现和最新进展,特别强调了钍和铀以外的锕系元素(即锕、镎、钚、镅、锔、锫和锎),因为它们源自人类活动,可以在环境中移动。本文结合历史背景回顾了环境中发现的和研究中使用的锕系同位素的核特性。然后,将锕系元素离子的配位化学特性与环境中天然存在的常见金属离子的配位化学特性进行对比。然后回顾了可能影响锕系元素生物地球化学的典型螯合剂。然后,介绍了金属蛋白在锕系元素生物地球化学中的作用,因为该领域的最新进展可能会对放射化学和核废料的长期管理产生影响。金属蛋白是自然界中无处不在的配体,但正如本综述中所讨论的那样,它们在锕系元素化学中却在很大程度上被忽视了,尤其是与传统的环境螯合剂相比。在不贬低丰富的天然锕系元素离子(即 Th4+ 和 UO22+)的重要性的前提下,本综述主要关注三价锕系元素,因为它们在核燃料循环、放射性废物管理、重元素研究以及最近的核医学等领域中非常普遍。此外,三价锕系元素与稀土元素在化学性质上有相似之处,最近在镧系元素结合螯合剂领域取得的突破可能会影响到锕系元素生物地球化学领域,下文将对此进行讨论。
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ACS Environmental Au
ACS Environmental Au 环境科学-
CiteScore
7.10
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0
期刊介绍: ACS Environmental Au is an open access journal which publishes experimental research and theoretical results in all aspects of environmental science and technology both pure and applied. Short letters comprehensive articles reviews and perspectives are welcome in the following areas:Alternative EnergyAnthropogenic Impacts on Atmosphere Soil or WaterBiogeochemical CyclingBiomass or Wastes as ResourcesContaminants in Aquatic and Terrestrial EnvironmentsEnvironmental Data ScienceEcotoxicology and Public HealthEnergy and ClimateEnvironmental Modeling Processes and Measurement Methods and TechnologiesEnvironmental Nanotechnology and BiotechnologyGreen ChemistryGreen Manufacturing and EngineeringRisk assessment Regulatory Frameworks and Life-Cycle AssessmentsTreatment and Resource Recovery and Waste Management
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Issue Publication Information Issue Editorial Masthead Biogeochemistry of Actinides: Recent Progress and Perspective Advancing Microbial Electrochemical H2O2 Synthesis by Tailoring the Surface Chemistry of Stereolithography-Derived 3D Pyrolytic Carbon Electrodes Evaluation of Natural Organic Additives as Eco-friendly Inhibitors for Calcium and Magnesium Scale Formation in Water Systems
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