State Key Laboratory of Organic Geochemistry, Guangdong Key Laboratory of Environmental Protection and Resources Utilization, and Guangdong-Hong Kong-Macao Joint Laboratory for Environmental Pollution and Control, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China; CAS Center for Excellence in Deep Earth Science, Guangzhou 510640, China; University of Chinese Academy of Sciences, Beijing 100049, China.
State Key Laboratory of Organic Geochemistry, Guangdong Key Laboratory of Environmental Protection and Resources Utilization, and Guangdong-Hong Kong-Macao Joint Laboratory for Environmental Pollution and Control, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China; CAS Center for Excellence in Deep Earth Science, Guangzhou 510640, China.
J Environ Sci (China). 2023 Aug;130:65-74. doi: 10.1016/j.jes.2022.07.023. Epub 2022 Jul 23.
Heterogeneous reaction of NO with mineral dust aerosol may play important roles in troposphere chemistry, and has been investigated by a number of laboratory studies. However, the influence of mineralogy on this reaction has not been well understood, and its impact on aerosol hygroscopicity is not yet clear. This work investigated heterogeneous reactions of NO (∼10 ppmv) with K-feldspar, illite, kaolinite, montmorillonite and Arizona Test Dust (ATD) at room temperature as a function of relative humidity (<1% to 80%) and reaction time (up to 24 hr). Heterogeneous reactivity towards NO was low for illite, kaolinite, montmorillonite and ATD, and uptake coefficients of NO, γ(NO), were determined to be around or smaller than 1×10; K-feldspar exhibited higher reactivity towards NO, and CaCO is most reactive among the nine mineral dust samples considered in this and previous work. After heterogeneous reaction with NO for 24 hr, increase in hygroscopicity was nearly insignificant for illite, kaolinite and montmorillonite, and small but significant for K-feldspar; in addition, large increase in hygroscopicity was observed for ATD, although the increase in hygroscopicity was still smaller than CaCO.
NO 与矿物粉尘气溶胶的非均相反应可能在对流层化学中起重要作用,已通过许多实验室研究进行了研究。然而,矿物学对该反应的影响尚未得到很好的理解,其对气溶胶吸湿性的影响尚不清楚。本工作研究了室温下(10 ppmv)NO 与钾长石、伊利石、高岭石、蒙脱石和亚利桑那州试验粉尘(ATD)之间的非均相反应,相对湿度(<1%至 80%)和反应时间(长达 24 小时)。伊利石、高岭石、蒙脱石和 ATD 对 NO 的非均相反应活性较低,NO 的吸收系数γ(NO)约为或小于 1×10;钾长石对 NO 的反应活性较高,在本工作和以前的工作中考虑的九种矿物粉尘样品中 CaCO3 最具反应性。与 NO 进行 24 小时的非均相反应后,伊利石、高岭石和蒙脱石的吸湿性增加几乎可以忽略不计,而钾长石的吸湿性略有增加;此外,ATD 的吸湿性大幅增加,尽管吸湿性的增加仍小于 CaCO3。