Updated global warming potentials of inhaled halogenated anesthetics, isoflurane and sevoflurane from new temperature dependent OH-kinetics.

IF 4.3 3区 环境科学与生态学 Q1 CHEMISTRY, ANALYTICAL
Sara Espinosa, Francisco Martínez, María Antiñolo, Ole J Nielsen, Elena Jiménez
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引用次数: 0

Abstract

Despite the use of scavenging systems in anesthesia machines, inhaled halogenated anesthetic gases (HAGs), such as isoflurane (CF3CHClOCHF2) and sevoflurane ((CF3)2CHOCH2F), are still emitted directly into the atmosphere. In 2014, their atmospheric concentrations were 0.097 ppt (isoflurane) and 0.13 pptv (sevoflurane). As halogenated species, their impact on global warming has to be known. Notably, the global warming potential at a time horizon of 100 years (GWP100 years) for sevoflurane differs between IPCC and WMO sources, creating regulatory uncertainty. For that reason, in this work GWP100 years for isoflurane and sevoflurane was reevaluated from the atmospheric chemical lifetimes, τOHHAG, derived from the kinetic study of the gas-phase reactions of hydroxyl (OH) radicals with the HAGs and the radiative efficiencies (REs) derived from the (IR) absorption cross sections in the atmospheric window (1500-500 cm-1). The temperature dependence of the OH-rate coefficients (k1(T) for isoflurane and k2(T) for sevoflurane) between 263 and 353 K was determined at 100 Torr by using the pulsed laser photolysis/laser-induced fluorescence technique. The obtained Arrhenius expressions are k1(T) = (1.1 ± 0.5) × 10-13 exp{-(1234 ± 144)/T} and k2(T) = (1.6 ± 0.7) × 10-12 exp{-(1065 ± 138)/T} cm3 molecule-1 s-1. At 272 K, a τOHHAG of 3.0 years for isoflurane and 1.2 years for sevoflurane were estimated relative to CH3CCl3 from k1 and k2. Moreover, the ultraviolet (UV) absorption cross sections were determined between 190 and 400 nm at 298 K, and the absorption was found to be negligible above 290 nm, indicating minimal photolysis by sunlight. In contrast, the IR absorption in the atmospheric window is significant and the IR absorption cross sections (4000-500 cm-1) were determined by Fourier Transform infrared spectroscopy. The lifetime-corrected radiative efficiencies (REs) were 0.44 and 0.30 W m-2 ppbv-1 for isoflurane and sevoflurane, respectively. From lifetime-corrected REs and τOHHAG, GWP100 years was estimated to be 508 for isoflurane (5% lower than IPCC/WMO values) and 125 for sevoflurane (36% lower than IPCC and 11% lower than WMO). These findings confirm isoflurane to be a high-GWP gas (above 150) according to the EU 2024 regulation, while sevoflurane does not meet the high-GWP threshold. A reassessment of the IPCC and WMO values is recommended.

从新的温度依赖oh动力学中更新吸入卤代麻醉药、异氟醚和七氟醚的全球变暖潜势。
尽管在麻醉机上使用了清除系统,吸入的卤化麻醉气体(hag),如异氟烷(CF3CHClOCHF2)和七氟烷((CF3)2CHOCH2F),仍然直接排放到大气中。2014年,它们的大气浓度分别为0.097 pptv(异氟烷)和0.13 pptv(七氟烷)。作为卤化物种,它们对全球变暖的影响必须为人所知。值得注意的是,七氟烷在100年时间范围内的全球变暖潜能值(GWP100年)在IPCC和WMO的资料中有所不同,造成了监管上的不确定性。因此,本文通过大气化学寿命τOHHAG和辐射效率REs对异氟烷和七氟烷的GWP100年进行了重新评估,该寿命τOHHAG来源于羟基(OH)自由基与hag气相反应的动力学研究,辐射效率(REs)来源于大气窗口(1500-500 cm-1)的红外吸收截面。利用脉冲激光光解/激光诱导荧光技术,测定了在100 Torr下,263 ~ 353 K之间oh -速率系数(异氟烷k1(T)和七氟烷k2(T))的温度依赖性。得到的Arrhenius表达式为k1(T) =(1.1±0.5)× 10-13 exp{-(1234±144)/T}, k2(T) =(1.6±0.7)× 10-12 exp{-(1065±138)/T} cm3分子-1 s-1。在272 K时,相对于CH3CCl3,从k1和k2估计异氟烷的τOHHAG为3.0年,七氟烷的τOHHAG为1.2年。此外,在298 K下,在190 ~ 400 nm之间测定了紫外吸收截面,在290 nm以上发现吸收可以忽略不计,表明太阳光的光解作用最小。相比之下,大气窗口的红外吸收显著,采用傅里叶变换红外光谱测定了红外吸收截面(4000-500 cm-1)。异氟烷和七氟烷的寿命校正辐射效率(REs)分别为0.44和0.30 W m-2 ppbv-1。根据寿命校正REs和τOHHAG,估计异氟烷的GWP100年为508年(比IPCC/WMO的值低5%),七氟烷的GWP100年为125年(比IPCC低36%,比WMO低11%)。这些研究结果证实,根据欧盟2024年的规定,异氟烷属于高gwp气体(高于150),而七氟烷不符合高gwp阈值。建议重新评估IPCC和WMO的值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Environmental Science: Processes & Impacts
Environmental Science: Processes & Impacts CHEMISTRY, ANALYTICAL-ENVIRONMENTAL SCIENCES
CiteScore
9.50
自引率
3.60%
发文量
202
审稿时长
1 months
期刊介绍: Environmental Science: Processes & Impacts publishes high quality papers in all areas of the environmental chemical sciences, including chemistry of the air, water, soil and sediment. We welcome studies on the environmental fate and effects of anthropogenic and naturally occurring contaminants, both chemical and microbiological, as well as related natural element cycling processes.
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