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Enhanced Reactive Uptake of Nonanal by Acidic Aerosols in the Presence of Particle-Phase Organics

机译:颗粒相有机物存在下酸性气溶胶对壬醛反应活性的增强

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An electrodynamic balance was used to examine the effect of the presence of particle-phase organics on the acid-catalyzed reactive uptake of nonanal (NL) vapor. Uptake experiments were conducted by using sulfuric acid (SA) particles, oleic acid/SA (hydrophobic), and levoglucosan/SA (hydrophilic) mixed particles with 6 ppm (approximately) gas-phase NL at about 3% relative humidity. SA reacted with the mixed organics prior to NL uptake to form organic products, denoted as OleA* and Levo*, and with NL to form hydrophobic NL* (particle-phase organics). Fresh SA particles had small mass increases (5%-13%) at the start of NL exposure (0-40 min) even though they are highly acidic. However, OleA*/SA mixed particles of about 30-70 wt% of OleA* took up NL swiftly during the first 40 min. For example, the mass increase of a 33 wt% OleA* particle jumped to 120%. As the organic product, NL*, accumulated, the uptake rate of SA particle increased and the mass increase surged to 150% at 100 min. Afterwards, the mass increase started to level off which yielded a sigmoid uptake curve. For OleA*/SA particles, the uptake rate gradually slowed down resulting in physical-absorption-like uptake kinetics. The physical uptake of NL by a pure OleA* surrogate was negligible (<1%) showing that the large uptake of OleA*/SA particles were attributed to the enhanced reactive uptake of NL in the presence of hydrophobic OleA*. Conversely, the hydrophilic Levo*/SA particles were incompatible with NL, and they showed insignificant enhanced uptake compared with the SA particles. Overall, the acidic uptake of NL is highly dependent on the chemical nature and weight percentages of particle-phase organics in mixed particles. Presence of hydrophobic organic materials in particles enhanced the reactive uptake of NL.
机译:使用电动平衡来检查颗粒相有机物的存在对酸催化的壬醛(NL)蒸气反应性吸收的影响。通过使用硫酸(SA)颗粒,油酸/ SA(疏水性)和左旋葡聚糖/ SA(亲水性)混合颗粒(相对湿度为约3%)(含6 ppm(约))的NL进行吸收实验。在NL吸收之前,SA与混合的有机物反应形成有机产物,表示为OleA *和Levo *,并与NL形成疏水性NL *(颗粒相有机物)。新鲜的SA颗粒在NL暴露开始(0-40分钟)时质量增加较小(5%-13%),即使它们是高酸性的。但是,在最初的40分钟内,约30-70 wt%的OleA *的OleA * / SA混合颗粒迅速吸收了NL。例如,33 wt%的OleA *颗粒的质量增加跃升至120%。随着有机产物NL *的积累,在100分钟时SA颗粒的吸收率增加,质量增加到150%。之后,质量增加开始趋于平稳,这产生了S形吸收曲线。对于OleA * / SA颗粒,吸收速率逐渐减慢,从而导致类似物理吸收的吸收动力学。纯OleA *替代物对NL的物理吸收微不足道(<1%),表明OleA * / SA颗粒的大量吸收归因于在疏水OleA *存在下NL的反应性吸收增加。相反,亲水的Levo * / SA颗粒与NL不相容,与SA颗粒相比,它们吸收的增加不明显。总体而言,NL的酸性吸收高度依赖于化学性质和混合颗粒中颗粒相有机物的重量百分比。颗粒中疏水有机材料的存在增强了NL的反应性吸收。

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  • 来源
    《Aerosol Science and Technology》 |2011年第7期|p.872-883|共12页
  • 作者

    Lap P. Chan Chak K. Chan;

  • 作者单位

    Department of Chemical and Biomolecular Engineering, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong Division of Environment, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 00:57:41

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