大气温度对β-石竹烯臭氧分解动力学的依赖性由稳定的预反应配合物控制。

IF 2.8 2区 化学 Q3 CHEMISTRY, PHYSICAL
Hengjia Ou, Kunpeng Chen
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引用次数: 0

摘要

挥发性有机化合物(VOCs)的大气寿命是由氧化动力学决定的,氧化动力学对温度的变化有潜在的敏感性。然而,由于实验数据有限,计算精度不高,温度对大挥发性有机化合物(如倍半萜)氧化动力学的影响仍未得到充分探讨。在这项研究中,我们通过明确地加入稳定的预反应配合物(SPCs),准确地模拟了大气中具有代表性的倍半萜β-石竹烯臭氧分解动力学的温度依赖性(243-313 K)。我们的研究结果表明,在内环C = C双键上形成的SPCs主要驱动温度依赖的臭氧分解动力学,因为它们形成初级臭氧化物(POZs)的能量势垒较低。这些内环SPCs也表现出正向反应和反向解离之间的平衡。相比之下,外环SPCs虽然热力学更稳定,但反应性较差,容易解离成β-石蜡烯和臭氧(O3)。这种机制上的差异可能解释了为什么在内环C = C双键上的O3环加成支配了β-石竹烯的臭氧分解动力学,尽管内环SPCs的相对丰度低于外环SPCs。计算动力学表明,指前因子为2.0 × 10-15 cm3分子-1 s-1,负活化能为-4.4 kJ mol-1。计算得到的温度依赖系数为529.8 K-1,与实验值(559±97 K-1)基本一致。结合spc的计算进一步支持了不同温度下伪一阶大气寿命的准确预测。总体而言,本研究表明,将SPCs纳入计算模型可以为模拟气候变化极端温度下VOC氧化动力学和大气寿命提供有效框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Atmospheric Temperature Dependence of β-Caryophyllene Ozonolysis Kinetics Is Governed by Stabilized Prereactive Complexes.

Atmospheric lifetime of volatile organic compounds (VOCs) is determined by oxidation kinetics, which is potentially sensitive to the change of temperature. However, the influence of temperature on the oxidation kinetics of large VOCs, such as sesquiterpenes, remains inadequately explored due to limited experimental data and insufficient accuracy of computations. In this study, we accurately simulate the temperature dependence (243-313 K) of ozonolysis kinetics of β-caryophyllene, a representative sesquiterpene in the atmosphere, by explicitly incorporating stabilized prereactive complexes (SPCs). Our results reveal that SPCs formed at the endocyclic C═C double bond primarily drive the temperature-dependent ozonolysis kinetics owing to their low energy barriers for forming primary ozonides (POZs). These endocyclic SPCs also exhibit a balance between the forward reaction and backward dissociation. In contrast, exocyclic SPCs, while more thermodynamically stable, are less reactive and tend to dissociate back into β-caryophyllene and ozone (O3). This mechanistic difference may explain why O3 cycloaddition at the endocyclic C═C double bond dominates the ozonolysis kinetics of β-caryophyllene, despite the lower relative abundance of endocyclic SPCs compared to the exocyclic SPCs. The computed kinetics exhibits a pre-exponential factor of 2.0 × 10-15 cm3 molecule-1 s-1 and a negative activation energy of -4.4 kJ mol-1. Our computed temperature dependence factor is 529.8 K-1, which agrees with the experimental value (559 ± 97 K-1) in previous measurements. The SPC-incorporated computation further supports the accurate prediction of the pseudo-first-order atmospheric lifetime at different temperatures. Overall, this study demonstrates that incorporating SPCs into computational models can provide an effective framework for simulating VOC oxidation kinetics and thus atmospheric lifetimes at the extreme temperatures in climate change.

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来源期刊
The Journal of Physical Chemistry A
The Journal of Physical Chemistry A 化学-物理:原子、分子和化学物理
CiteScore
5.20
自引率
10.30%
发文量
922
审稿时长
1.3 months
期刊介绍: The Journal of Physical Chemistry A is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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