Recent Progress in Advanced Catalytic Strategies for C─F Bond Cleavage in Waste Refrigerants: A Review

IF 19 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Advanced Functional Materials Pub Date : 2025-01-28 DOI:10.1002/adfm.202420883
Yuting Wang, Zhuang Yang, Hao Xiu, Fan Fan, Pan An, Yongpeng Cui, Yajun Wang, Wenqing Yao
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Abstract

The degradation of fluorinated refrigerants, known for their highly stable carbon-fluorine (C─F) bonds, poses significant environmental and technical challenges. This review addresses these challenges by analyzing two core degradation mechanisms: molecular polarization (MP) and free radical attack (FRA), and exploring their applications in thermal catalytic and photocatalytic processes. MP redistributes electron density to weaken C─F bonds, facilitating adsorption and bond cleavage, while radical attack involves reactive species that directly break chemical bonds. However, both mechanisms have limitations: MP alone may lack the kinetic drive for dissociation, and radical-based methods often suffer from low selectivity, short radical lifetimes, and the formation of toxic intermediates. The section on thermal catalytic degradation discusses how elevated temperatures enhance bond cleavage through MP, addressing adsorption challenges and accelerating dissociation. The part on photocatalytic degradation focuses on the role of light-activated processes in generating reactive radicals and facilitating bond breaking, with an emphasis on visible and ultraviolet light-driven reactions. The review concludes by exploring the potential of hybrid catalytic systems that combine thermal and photocatalytic processes, providing insights into the complementary use of these mechanisms for the degradation of persistent fluorinated compounds.

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废制冷剂中C─F键裂解的先进催化策略研究进展
含氟制冷剂以其高度稳定的碳氟(C─F)键而闻名,其降解构成了重大的环境和技术挑战。本文通过分析分子极化(MP)和自由基攻击(FRA)两种核心降解机制,探讨其在热催化和光催化过程中的应用。MP重新分配电子密度以削弱C─F键,促进吸附和键裂解,而自由基攻击涉及直接破坏化学键的活性物质。然而,这两种机制都有局限性:单独的MP可能缺乏解离的动力学驱动,并且基于自由基的方法通常存在选择性低、自由基寿命短和形成有毒中间体的问题。热催化降解部分讨论了高温如何通过MP增强键裂解,解决吸附挑战并加速解离。光催化降解部分侧重于光激活过程在产生活性自由基和促进键断裂中的作用,重点是可见光和紫外光驱动的反应。本综述最后探讨了结合热催化和光催化过程的混合催化系统的潜力,为这些机制在降解持久性氟化化合物方面的互补利用提供了见解。
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来源期刊
Advanced Functional Materials
Advanced Functional Materials 工程技术-材料科学:综合
CiteScore
29.50
自引率
4.20%
发文量
2086
审稿时长
2.1 months
期刊介绍: Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week. Advanced Functional Materials is known for its rapid and fair peer review, quality content, and high impact, making it the first choice of the international materials science community.
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