有机气溶结构的大小依赖性
Daniel P Veghte1, Muhammad Bilal Altaf, Miriam Arak Freedman
1Department of Chemistry, The Pennsylvania State University , 104 Chemistry Building, University Park, Pennsylvania 16802, United States.
Journal of the American Chemical Society
|October 16, 2013
概括
气溶颗粒相位分离,对于大气化学和气候至关重要,取决于颗粒大小. 较小的粒子 (<170-270 nm) 保持不分离,而较大的粒子呈现相位分离.
科学领域:
- 大气化学 大气化学
- 气候科学 气候科学
- 材料科学 材料科学 材料科学
背景情况:
- 不同质的大气化学和气候影响受到气溶颗粒的组成和结构的影响.
- 了解气溶颗粒中的化合物的内部排列是预测它们对环境的影响的关键.
研究的目的:
- 为了研究模型有机气溶颗粒的相分离行为.
- 为了确定颗粒大小对混合硫酸和有机酸气溶的内部结构的影响.
主要方法:
- 使用冷传输电子显微镜 (cryo-TEM) 可视化气溶颗粒的内部结构.
- 检查的模型是有机气溶,由硫酸与酸或皮梅酸混合而成.
主要成果:
- 在酸混合物中小于170nm的粒子和在pimelic酸混合物中小于270nm的粒子中没有观察到相分离.
- 较大的气溶颗粒 (酸≥170nm,酸≥270nm) 呈现出分相,部分包裹的结构.
结论:
- 气溶颗粒相位分离非常依赖于颗粒大小.
- 尺寸依赖的相位分离对气溶气候相互作用和大气化学模型有重大影响.
相关概念视频
Molecular Structure and Acidity
15.0K
An acid can be deprotonated to form a conjugate base or an anion. If the produced anion is more stable, then the acid is stronger. On the contrary, if the anion is unstable, then the acid is weaker. Hence, to determine the acidity of the compound, the stability of its conjugate base is studied using various factors.
The size effect explains the change in atomic size on acidity. When comparing the acids formed from elements that belong to the same column in the periodic table, their atomic sizes...
The size effect explains the change in atomic size on acidity. When comparing the acids formed from elements that belong to the same column in the periodic table, their atomic sizes...
15.0K
UV–Vis Spectroscopy: Woodward–Fieser Rules
30.7K
UV–Visible absorption spectra of conjugated dienes arise from the lowest energy π → π* transitions. The light-absorbing part of the molecule is called the chromophore, and the substituents directly attached to the chromophore are called auxochromes. A strong correlation exists between the absorption maxima, λmax, and the structure of a conjugated π system. The Woodward–Fieser rules predict the value of λmax for a...
30.7K
Resonance and Hybrid Structures
20.1K
According to the theory of resonance, if two or more Lewis structures with the same arrangement of atoms can be written for a molecule, ion, or radical, the actual distribution of electrons is an average of that shown by the various Lewis structures.
Resonance Structures and Resonance Hybrids
The Lewis structure of a nitrite anion (NO2−) may actually be drawn in two different ways, distinguished by the locations of the N–O and N=O bonds.
Resonance Structures and Resonance Hybrids
The Lewis structure of a nitrite anion (NO2−) may actually be drawn in two different ways, distinguished by the locations of the N–O and N=O bonds.
20.1K
Polymers: Molecular Weight Distribution
4.0K
For any given polymer, the weight average molecular weight (Mw) is higher than, if not equal to, the number average molecular weight (Mn). The only situation in which the weight average molecular weight and the number average molecular weight are equal is when a polymer consists only of chains with equal molecular weight. However, this never happens in a synthetic polymer, since it is difficult to control the polymerization process up to a molecular level with accuracy to a hundred percent.
4.0K
Precipitate Formation and Particle Size Control
5.8K
In precipitation gravimetry, the precipitating agent should react specifically or selectively with the analyte. While a specific reagent reacts with the analyte alone, a selective reagent can react with a limited number of chemical species.
The obtained precipitate should be either a pure substance of known composition or easily converted to one by a simple process, such as ignition or drying. In addition, the precipitate should be insoluble and easily filterable. In general, filterability...
The obtained precipitate should be either a pure substance of known composition or easily converted to one by a simple process, such as ignition or drying. In addition, the precipitate should be insoluble and easily filterable. In general, filterability...
5.8K
Aromatic Hydrocarbon Anions: Structural Overview
3.5K
Neutral hydrocarbons like cyclopentadiene with an odd number of carbon atoms and one intervening CH2 group in the ring are not aromatic. Cyclopentadiene with 4 π electrons does not satisfy the 4n + 2 π electron rule. Additionally, the intervening CH2 group is sp3 hybridized and lacks a vacant p orbital, thereby interrupting the overlap of p orbitals in a continuous manner and preventing the delocalization of π electrons throughout the ring.
Due to the absence of continuous...
Due to the absence of continuous...
3.5K


