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大气中α-蒎烯和β-石竹烯臭氧分解产物的云激活潜力。

Cloud Activation Potentials for Atmospheric α-Pinene and β-Caryophyllene Ozonolysis Products.

作者信息

Gray Bé Ariana, Upshur Mary Alice, Liu Pengfei, Martin Scot T, Geiger Franz M, Thomson Regan J

机构信息

Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States.

John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts 02138, United States.

出版信息

ACS Cent Sci. 2017 Jul 26;3(7):715-725. doi: 10.1021/acscentsci.7b00112. Epub 2017 Jul 5.

Abstract

The formation of atmospheric cloud droplets due to secondary organic aerosol (SOA) particles is important for quantifying the Earth's radiative balance under future, possibly warmer, climates, yet is only poorly understood. While cloud activation may be parametrized using the surface tension depression that coincides with surfactant partitioning to the gas-droplet interface, the extent to which cloud activation is influenced by both the chemical structure and reactivity of the individual molecules comprising this surfactant pool is largely unknown. We report herein considerable differences in the surface tension depression of aqueous pendant droplets that contain synthetically prepared ozonolysis products derived from α-pinene and β-caryophyllene, the most abundant of the monoterpenes and sesquiterpenes, respectively, that are emitted over the planet's vast forest ecosystems. Oxidation products derived from β-caryophyllene were found to exhibit significantly higher surface activity than those prepared from α-pinene, with the critical supersaturation required for cloud droplet activation reduced by 50% for β-caryophyllene aldehyde at 1 mM. These considerable reductions in the critical supersaturation were found to coincide with free energies of adsorption that exceed ∼25 kJ/mol, or just one hydrogen bond equivalent, depending on the ammonium sulfate and oxidation product concentration in the solution. Additional experiments showed that aldehyde-containing oxidation products exist in equilibrium with hydrated forms in aqueous solution, which may modulate their bulk solubility and surface activity. Equilibration time scales on the order of 10 to 10 s calculated for micrometer-sized aerosol particles indicate instantaneous surface tension depression in the activation processes leading to cloud formation in the atmosphere. Our findings highlight the underlying importance of molecular structure and reactivity when considering cloud condensation activity in the presence of SOA particles.

摘要

二次有机气溶胶(SOA)颗粒导致大气云滴的形成对于量化未来可能更温暖气候下地球的辐射平衡非常重要,但目前对此了解甚少。虽然云激活可以通过与表面活性剂分配到气-液界面相吻合的表面张力降低来参数化,但构成该表面活性剂库的单个分子的化学结构和反应性对云激活的影响程度在很大程度上尚不清楚。我们在此报告了含有合成制备的α-蒎烯和β-石竹烯臭氧分解产物的悬垂水滴表面张力降低的显著差异,α-蒎烯和β-石竹烯分别是在地球广阔森林生态系统中排放的最丰富的单萜和倍半萜。发现源自β-石竹烯的氧化产物比源自α-蒎烯的氧化产物表现出显著更高的表面活性,对于1 mM的β-石竹烯醛,云滴激活所需的临界过饱和度降低了50%。发现这些临界过饱和度的显著降低与超过约25 kJ/mol的吸附自由能相吻合,或者仅相当于一个氢键,这取决于溶液中硫酸铵和氧化产物的浓度。额外的实验表明,含醛氧化产物在水溶液中与水合形式处于平衡状态,这可能会调节它们的整体溶解度和表面活性。对于微米级气溶胶颗粒计算得出的10到10秒量级的平衡时间尺度表明,在导致大气中云形成的激活过程中表面张力瞬间降低。我们的研究结果突出了在考虑存在SOA颗粒时云凝结活性时分子结构和反应性的潜在重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c620/5532715/5a5ce09fd8e6/oc-2017-00112q_0001.jpg

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