Oxalate Formation Enhanced by Fe-Containing Particles and Environmental Implications

• Published in: Environmental science & technology Vol. 53; no. 3; pp. 1269 - 1277
• Main Authors: Zhang, Guohua, Lin, Qinhao, Peng, Long, Yang, Yuxiang, Jiang, Feng, Liu, Fengxian, Song, Wei, Chen, Duohong, Cai, Zhang, Bi, Xinhui, Miller, Mark, Tang, Mingjin, Huang, Weilin, Wang, Xinming, Peng, Ping’an, Sheng, Guoying
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 05-02-2019
• Subjects: Acetic acid; Chemical composition; Computer simulation; Diurnal; Iron; Mass spectrometry; Mass spectroscopy; Moisture content; Organic chemistry; Organic compounds; Oxalic acid; Oxidation; Particle mass; Particulates; Pyruvaldehyde; Reactive oxygen species; Relative humidity; Water content
• ISSN: 0013-936X; 1520-5851
• DOI: 10.1021/acs.est.8b05280

We used a single particle mass spectrometry to online detect chemical compositions of individual particles over four seasons in Guangzhou. Number fractions (Nfs) of all the measured particles that contained oxalate were 1.9%, 5.2%, 25.1%, and 15.5%, whereas the Nfs of Fe-containing particles that were internally mixed with oxalate were 8.7%, 23.1%, 45.2%, and 31.2% from spring to winter, respectively. The results provided the first direct field measurements for the enhanced formation of oxalate associated with Fe-containing particles. Other oxidized organic compounds including formate, acetate, methylglyoxal, glyoxylate, purivate, malonate, and succinate were also detected in the Fe-containing particles. It is likely that reactive oxidant species (ROS) via Fenton reactions enhanced the formation of these organic compounds and their oxidation product oxalate. Gas-particle partitioning of oxalic acid followed by coordination with Fe might also partly contribute to the enhanced oxalate. Aerosol water content likely played an important role in the enhanced oxalate formation when the relative humidity is >60%. Interactions with Fe drove the diurnal variation of oxalate in the Fe-containing particles. The study could provide a reference for model simulation to improve understanding on the formation and fate of oxalate, and the evolution and climate impacts of particulate Fe.