Institute of Chemical Physics, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, 100081, PR China.
Institute of Chemical Physics, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, 100081, PR China; College of Resource and Environment Sciences, Xinjiang University, Urumqi, 830046, PR China.
Chemosphere. 2020 Feb;240:124744. doi: 10.1016/j.chemosphere.2019.124744. Epub 2019 Sep 7.
The heterogeneous reactions of α-AlO particles with a mixture of ozone (∼50 ppm) and isoprene (∼50 ppm) were studied as a function of relative humidities (RHs). The reactions were monitored in real time through the microscopic Fourier transform infrared (micro-FTIR) spectrometer. The results show that the presence of ozone leads to the rapid conversion of isoprene to carboxylate (COO) ions on the surfaces of α-AlO particles in the initial stage. The water significantly suppresses the formation of the carboxylate ions. For the isoprene ozonolysis reaction on the α-AlO particles, the reactive uptake coefficient is strongly suppressed by over a factor of 8 when the RH increases from 8% to 89%. The negative correlation between RH with the secondary organic aerosol (SOA) produced by isoprene ozonolysis plays a key role in the actual atmospheric environment under high humidity. Our results may provide insight into the ozonolysis process of biogenic alkenes over mineral aerosol surfaces with the influence of RHs.
α-AlO 颗粒与臭氧(∼50ppm)和异戊二烯(∼50ppm)混合物的多相反应随相对湿度(RH)的变化而变化。通过微观傅里叶变换红外(micro-FTIR)光谱仪实时监测反应。结果表明,在初始阶段,臭氧的存在导致异戊二烯在α-AlO 颗粒表面迅速转化为羧酸盐(COO)离子。水显著抑制了羧酸盐离子的形成。对于α-AlO 颗粒上的异戊二烯臭氧分解反应,当 RH 从 8%增加到 89%时,反应性吸收系数被强烈抑制超过 8 倍。RH 与异戊二烯臭氧分解产生的二次有机气溶胶(SOA)之间的负相关在高湿度实际大气环境中起着关键作用。我们的结果可能为 RHs 影响下矿物气溶胶表面上生物烯的臭氧分解过程提供了一些见解。