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首页> 外文期刊>Atmospheric environment >Direct observation of polymerization in the oleic acid-ozone heterogeneous reaction system by photoelectron resonance capture ionization aerosol mass spectrometry
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Direct observation of polymerization in the oleic acid-ozone heterogeneous reaction system by photoelectron resonance capture ionization aerosol mass spectrometry

机译:通过光电子共振捕获电离气溶胶质谱法直接观察油酸-臭氧非均相反应体系中的聚合反应

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High molecular weight products of the ozonolysis reaction of particle-phase 9-octadecenoic acid (oleic acid) have been studied by photoelectron resonance capture ionization (PERCI) mass spectrometry (MS). Oleic acid particles (d_g = 202 nm, σ_g = 1.97) were reacted with ozone (1.8 x 10~(-4) atm) in a flow reactor at reaction times of 8 and 23 s. Particles were sampled on-line with a differentially pumped particle inlet and chemically analyzed by PERCI-MS. PERCI is a soft ionization method that permits the direct measurement of relatively high molecular weight compounds, facilitating molecular identification. In addition to cyclic oxygenates, such as secondary ozonides and geminal diperoxides that were reported previously, we demonstrate the formation of polymers at the particle surface. Polymer formation is proposed to proceed via addition of a Criegee intermediate to oleic acid forming an α-acyloxyalkyl hydroperoxide, and subsequent additions of Criegee intermediates to this initial addition product and later generations. Ultimately, polyanhydrides are formed through dehydration of these α-acyloxyalkyl hydroperoxide intermediates. The highest molecular weight, unfragmented polyanhydride has been measured at 963 U, resulting from the successive addition of four Criegee intermediates to a parent oleic acid molecule. The low volatility of these products, coupled with their high polarity, may alter particle phase hygroscopicity that can enhance the cloud condensation properties of these particles. Further, the polymer products formed at the particles' surface may significantly alter diffusion of reactive gases, thereby affecting the reactive uptake of atmospheric trace gases and impacting the oxidizing capacity of the atmosphere.
机译:已通过光电子共振捕获电离(PERCI)质谱(MS)研究了颗粒相9-十八碳烯酸(油酸)的臭氧分解反应的高分子量产物。油酸颗粒(d_g = 202 nm,σ_g= 1.97)在流动反应器中与臭氧(1.8 x 10〜(-4)atm)反应时间为8和23 s。使用差分泵送的颗粒入口在线采样颗粒,并通过PERCI-MS进行化学分析。 PERCI是一种软电离方法,可以直接测量相对较高分子量的化合物,从而有助于分子鉴定。除了先前报道的环状含氧化合物(如仲氧化氮和双氧化二锗)外,我们还证明了聚合物在颗粒表面的形成。提出通过向油酸中加入Criegee中间体以形成α-酰氧基烷基氢过氧化物来进行聚合物形成,然后将Criegee中间体随后加入该初始加成产物和后代中。最终,通过这些α-酰氧基烷基氢过氧化物中间体的脱水形成聚酸酐。最高分子量的无碎片聚酸酐的测量值为963 U,这是由于将四个Criegee中间体连续添加到母体油酸分子中而产生的。这些产品的低挥发性及其高极性可能会改变颗粒相的吸湿性,从而增强这些颗粒的云凝结特性。此外,在颗粒表面形成的聚合物产物可显着改变反应性气体的扩散,从而影响大气中痕量气体的反应性吸收并影响大气的氧化能力。

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