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Effects of pH on Interfacial Ozonolysis of alpha-Terpineol

机译:pH对α-萜烯醇界面臭氧溶解的影响

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摘要

Acidity changes the physical properties of atmospheric aerosol particles and the mechanisms of reactions that occur therein and on the surface. Here, we used surface-sensitive pneumatic ionization mass spectrometry to investigate the effects of pH on the heterogeneous reactions of aqueous alpha-terpineol (C10H17OH), a representative monoterpene alcohol, with gaseous ozone. Rapid (<= 10 mu s) ozonolysis of alpha-terpineol produced Criegee intermediates (CIs, zwitterionic/diradical carbonyl oxides) on the surface of water microjets. We studied the effects of microjet bulk pH (1-11) on the formation of functionalized carboxylate and alpha-hydroxy-hydroperoxide chloride adduct (HH-Cl-) products generated by isomerization and hydration of alpha-terpineol CIs, respectively. Compared with the signal at pH approximate to 6, the mass spectral signal of HH-Cl- was less intense under both basic and more acidic conditions, whereas the intensity of the functionalized carboxylate signal increased with increasing pH up to 4 and then remained constant. The decrease of HH-Cl- signals at bulk pH values of >6 is attributable to the accumulation of OH- at the air-water interface that suppresses the relative abundance of hydrophilic HH and Cl-. The present study suggests that alpha-terpineol in ambient aqueous organic aerosols will be converted into much lower volatile and potentially toxic organic hydroperoxides during the heterogeneous ozonolysis.
机译:酸度变化大气气溶胶颗粒的物理性质和出现在其中并在表面上反应的机理。在这里,我们使用的表面敏感气动喷雾电离质谱研究pH对水性α-萜品醇(C10H17OH),具有代表性的单萜醇,用气态臭氧的非均相反应的影响。 α-松油醇的快速(<= 10亩S)臭氧分解产生克里奇中间体(顺式,两性离子/二基羰基氧)水的微射流的表面上。我们对官能化羧酸盐和α-羟基 - 氢过氧化物加合物氯化物分别由异构化和α-松油醇证明书水合,生成(HH-氯离子)产物的形成研究微射流主体pH(1-11)的效果。用pH接近6的信号进行比较,HH-氯离子的质谱信号是碱性和更酸性条件下较不强烈,而官能化羧酸的信号的强度随着pH增加多达4增加,然后保持恒定。 HH-氯离子信号中的> 6散装的pH值的减少是由于OH-的在空气 - 水界面抑制亲水HH和Cl-的相对丰度的积累。本研究表明,α-萜品醇中的环境水有机气溶胶将异构臭氧分解过程中被转化成低得多的易失性和潜在毒性的有机氢过氧化物。

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