臭氧分解
臭氧
化学
激进的
温室气体
产量(工程)
制冷剂
全球变暖潜力
大气(单位)
光化学
臭氧消耗
环境化学
环境科学
大气科学
有机化学
热力学
物理
气体压缩机
生态学
生物
地质学
作者
Max R. McGillen,Zachary T. P. Fried,M. Anwar H. Khan,Keith T. Kuwata,Connor M. Martin,Simon O’Doherty,Francesco Pecere,Dudley E. Shallcross,Kieran Stanley,Kexin Zhang
标识
DOI:10.1073/pnas.2312714120
摘要
Hydrofluoroolefins are being adopted as sustainable alternatives to long-lived fluorine- and chlorine-containing gases and are finding current or potential mass-market applications as refrigerants, among a myriad of other uses. Their olefinic bond affords relatively rapid reaction with hydroxyl radicals present in the atmosphere, leading to short lifetimes and proportionally small global warming potentials. However, this type of functionality also allows reaction with ozone, and whilst these reactions are slow, we show that the products of these reactions can be extremely long-lived. Our chamber measurements show that several industrially important hydrofluoroolefins produce CHF 3 (fluoroform, HFC-23), a potent, long-lived greenhouse gas. When this process is accounted for in atmospheric chemical and transport modeling simulations, we find that the total radiative effect of certain compounds can be several times that of the direct radiative effect currently recommended by the World Meteorological Organization. Our supporting quantum chemical calculations indicate that a large range of exothermicity is exhibited in the initial stages of ozonolysis, which has a powerful influence on the CHF 3 yield. Furthermore, we identify certain molecular configurations that preclude the formation of long-lived greenhouse gases. This demonstrates the importance of product quantification and ozonolysis kinetics in determining the overall environmental impact of hydrofluoroolefin emissions.
科研通智能强力驱动
Strongly Powered by AbleSci AI