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拉曼微光谱和振动和频产生光谱作为大小分辨的海洋喷雾气溶胶粒子体相和表面成分的探针。

Raman microspectroscopy and vibrational sum frequency generation spectroscopy as probes of the bulk and surface compositions of size-resolved sea spray aerosol particles.

机构信息

Department of Chemistry, University of Iowa, Iowa City, Iowa 52242, USA.

出版信息

Phys Chem Chem Phys. 2013 May 7;15(17):6206-14. doi: 10.1039/c3cp43899f.

Abstract

Sea spray aerosol (SSA) represents one of the largest aerosol components in our atmosphere. SSA plays a major role in influencing climate; however the overall impacts remain poorly understood due to the overall chemical complexity. SSA is comprised of a mixture of inorganic and organic components in varying proportions that change as a function of particle size and seawater composition. In this study, nascent SSA particles were produced using breaking waves, resulting in compositions and sizes representative of the open ocean. The composition of individual SSA particles ranging in size from ca. 0.15 to 10 μm is measured using Raman microspectroscopy, while the interfacial composition of collections of size-resolved particles is probed by sum frequency generation (SFG). Raman spectra of single particles have bands in the 980 to 1030 cm(-1) region associated with the symmetric stretch of the sulfate anion, the 2800 to 3000 cm(-1) region associated with carbon-hydrogen stretches, and from 3200-3700 cm(-1) associated with the oxygen-hydrogen stretches of water. The relative intensities of these features showed a strong dependence on particle size. In particular, submicrometer particles exhibited a larger amount of organic matter compared to supermicrometer particles. However, for external surfaces of homogeneous SSA particles (i.e. particles without a solid inclusion), and also the interfaces of mixed-phase particles, there was a strong SFG response in the aliphatic C-H stretching region for both sub- and supermicrometer particles. This finding suggests that organic material present in supermicrometer particles primarily resides at the interface. The presence of methylene contributions in the SFG spectra indicated disordered alkyl chains, in contrast to what one might expect for a surfactant layer on a sea salt particle. Changes in peak frequencies and relative intensities in the C-H stretching region are seen for some particles after the addition of bacteria, phytoplankton, and growth medium to the seawater. This study provides new insights into the bulk and surface composition of SSA particles and represents a step forward in our understanding of this globally abundant aerosol. It also provides insights into the development of model systems for SSA that may more accurately represent the organic layer at the surface.

摘要

海雾气溶胶(SSA)是大气中最大的气溶胶成分之一。SSA 在影响气候方面起着重要作用;然而,由于整体化学复杂性,其整体影响仍未被充分了解。SSA 由无机和有机成分的混合物组成,其比例随粒径和海水成分的变化而变化。在这项研究中,使用破碎波产生初生的 SSA 颗粒,从而产生具有代表性的开阔海洋的组成和大小的颗粒。使用拉曼微光谱测量尺寸在约 0.15 至 10 μm 范围内的单个 SSA 颗粒的组成,而通过和频产生(SFG)探测大小分辨颗粒的集合体的界面组成。单个颗粒的拉曼光谱在 980 至 1030 cm(-1) 区域有与硫酸根阴离子对称伸缩相关的谱带,在 2800 至 3000 cm(-1) 区域有与碳-氢键伸缩相关的谱带,在 3200-3700 cm(-1) 区域有与水的氧-氢键伸缩相关的谱带。这些特征的相对强度强烈依赖于颗粒尺寸。特别是,亚微米颗粒比超微米颗粒表现出更多的有机物。然而,对于均匀的 SSA 颗粒的外表面(即没有固体包含物的颗粒),以及混合相颗粒的界面,亚微米和超微米颗粒在脂肪族 C-H 伸缩区域都有很强的 SFG 响应。这一发现表明,超微米颗粒中存在的有机物质主要存在于界面处。SFG 光谱中的亚甲基贡献表明存在无序的烷基链,这与人们对海盐颗粒表面的表面活性剂层的预期形成鲜明对比。向海水中添加细菌、浮游植物和生长培养基后,一些颗粒的 C-H 伸缩区域的峰值频率和相对强度发生了变化。这项研究提供了对 SSA 颗粒体相和表面组成的新见解,代表了对这种全球丰富气溶胶的理解的一个进步。它还为 SSA 模型系统的发展提供了新的见解,这些模型系统可能更准确地代表表面的有机层。

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