Huabin Dong
Chinese Academy of Sciences
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Publication
Featured researches published by Huabin Dong.
Journal of Geophysical Research | 2014
Shinji Kudo; Hiroshi Tanimoto; Satoshi Inomata; Shinji Saito; Xiaole Pan; Yugo Kanaya; Fumikazu Taketani; Zifa Wang; H. Chen; Huabin Dong; Meigen Zhang; Kazuyo Yamaji
Open crop residue burning is one of the major sources of air pollutants including the precursors of photooxidants like ozone and secondary organic aerosol. We made measurements of trace gases including nonmethane volatile organic compounds (NMVOCs) in a rural area in central East China in June 2010. During the campaign, we identified six biomass burning events in total through the simultaneous enhancement of carbon monoxide and acetonitrile. Four cases represented fresh plumes ( 3 h after emission), as determined by photochemical age. While we were not able to quantify formic acid, we identified an enhancement of major oxygenated volatile organic compounds (OVOCs) as well as low molecular alkanes and alkenes, and aromatic hydrocarbons in these plumes. The observed normalized excess mixing ratios (NEMRs) of OVOCs and alkenes showed dependence on air mass age, even in fresh smoke plumes, supporting the view that these species are rapidly produced and destructed, respectively, during plume evolution. Based on the NEMR data in the fresh plumes, we calculated the emission factors (EFs) of individual NMVOC. The comparison to previous reports suggests that the EFs of formaldehyde and acetic acid have been overestimated, while those of alkenes have been underestimated. Finally, we suggest that open burning of wheat residue in China releases about 0.34 Tg NMVOCs annually. If we applied the same EFs to all crops, the annual NMVOC emissions would be 2.33 Tg. The EFs of speciated NMVOCs can be used to improve the existing inventories.
Journal of Environmental Sciences-china | 2016
Yuhan Liu; Keding Lu; Huabin Dong; Xin Li; Peng Cheng; Qi Zou; Yusheng Wu; Xingang Liu; Yuanhang Zhang
In the last four decades, various techniques including spectroscopic, wet chemical and mass spectrometric methods, have been developed and applied for the detection of ambient nitrous acid (HONO). We developed a HONO detection system based on long path photometry which consists of three independent modules i.e., sampling module, fluid propulsion module and detection module. In the propulsion module, solenoid pumps are applied. With solenoid pumps the pulsed flow can be computer controlled both in terms of pump stroke volume and pulse frequency, which enables the attainment of a very stable flow rate. In the detection module, a customized Liquid Waveguide Capillary Cell (LWCC) is used. The customized LWCC pre-sets the optical fiber in-coupling with the liquid wave guide, providing the option of fast startup and easy maintenance of the absorption photometry. In summer 2014, our system was deployed in a comprehensive campaign at a rural site in the North China Plain. More than one month of high quality HONO data spanning from the limit of detection to 5ppb were collected. Intercomparison of our system with another established system from Forschungszentrum Juelich is presented and discussed. In conclusion, our instrument achieved a detection limit of 10pptV within 2min and a measurement uncertainty of 7%, which is well suited for investigation of the HONO budget from urban to rural conditions in China.
Science of The Total Environment | 2018
Zhaofeng Tan; Keding Lu; Meiqing Jiang; Rong Su; Huabin Dong; Limin Zeng; Shaodong Xie; Qinwen Tan; Yuanhang Zhang
We present the in-situ measurements in Chengdu, a major city in south west of China, in September 2016. The concentrations of ozone and its precursor were measured at four sites. Although the campaign was conducted in early autumn, up to 100 ppbv (parts per billion by volume) daily maximum ozone was often observed at all sites. The observed ozone concentrations showed good agreement at all sites, which implied that ozone pollution is a regional issue in Chengdu. To better understand the ozone formation in Chengdu, an observation based model is used in this study to calculate the ROx radical concentrations (ROx = OH + HO2 + RO2) and ozone production rate (P(O3)). The model predicts OH daily maximum is in the range of 4-8 × 106 molecules cm-3, and HO2 and RO2 are in the range of 3-6 × 108 molecules cm-3. The modelled radical concentrations show a distinct difference between ozone pollution and attainment period. The relative incremental reactivity (RIR) results demonstrate that anthropogenic VOCs reduction is the most efficient way to mitigate ozone pollution at all sites, of which alkenes dominate >50% of the ozone production. Empirical kinetic modelling approach shows that three out of four sites are under the VOC-limited regime, while Pengzhou is in a transition regime due to the local petrochemical industry. The ozone budget analysis showed that the local ozone production driven by the photochemical process is important to the accumulation of ozone concentrations.
Atmospheric Chemistry and Physics | 2018
Zhaofeng Tan; Franz Rohrer; Keding Lu; Xuefei Ma; Birger Bohn; Sebastian Broch; Huabin Dong; Hendrik Fuchs; Georgios I. Gkatzelis; Andreas Hofzumahaus; F. Holland; Xin Li; Ying Liu; Yuhan Liu; Anna Novelli; Min Shao; Haichao Wang; Yusheng Wu; Limin Zeng; Min Hu; Astrid Kiendler-Scharr; Andreas Wahner; Yuanhang Zhang
The first wintertime in situ measurements of hydroxyl (OH), hydroperoxy (HO2) and organic peroxy (RO2) radicals (ROx= OH+HO2+RO2) in combination with observations of total reactivity of OH radicals, kOH in Beijing are presented. The field campaign “Beijing winter finE particle STudy – Oxidation, Nucleation and light Extinctions” (BEST-ONE) was conducted at the suburban site Huairou near Beijing from January to March 2016. It aimed to understand oxidative capacity during wintertime and to elucidate the secondary pollutants’ formation mechanism in the North China Plain (NCP). OH radical concentrations at noontime ranged from 2.4× 106 cm−3 in severely polluted air (kOH ∼ 27s−1) to 3.6× 106 cm−3 in relatively clean air (kOH ∼ 5s−1). These values are nearly 2-fold larger than OH concentrations observed in previous winter campaigns in Birmingham, Tokyo, and New York City. During this campaign, the total primary production rate of ROx radicals was dominated by the photolysis of nitrous acid accounting for 46 % of the identified primary production pathways for ROx radicals. Other important radical sources were alkene ozonolysis (28 %) and photolysis of oxygenated organic compounds (24 %). A box model was used to simulate the OH, HO2 and RO2 concentrations based on the observations of their longlived precursors. The model was capable of reproducing the observed diurnal variation of the OH and peroxy radicals during clean days with a factor of 1.5. However, it largely underestimated HO2 and RO2 concentrations by factors up to 5 during pollution episodes. The HO2 and RO2 observed-tomodeled ratios increased with increasing NO concentrations, indicating a deficit in our understanding of the gas-phase chemistry in the high NOx regime. The OH concentrations observed in the presence of large OH reactivities indicate that atmospheric trace gas oxidation by photochemical processes can be highly effective even during wintertime, thereby facilitating the vigorous formation of secondary pollutants.
quantum electronics and laser science conference | 2009
Anna P. M. Michel; Peter Q. Liu; June K. Yeung; Paul Corrigan; Mary Lynn Baeck; Xiaole Pan; Huabin Dong; Zifa Wang; Timothy Day; James A. Smith; Fred Moshary; Claire F. Gmachl
A widely tunable, external cavity quantum cascade laser was used in the deployment of an open-path sensor for the measurement of water vapor, ozone, ammonia, and carbon dioxide in the urban atmosphere of Beijing, China.
Atmospheric Chemistry and Physics | 2013
Yele Sun; Z. F. Wang; Pingqing Fu; Ting Yang; Qi Jiang; Huabin Dong; J. Li; J. J. Jia
Atmospheric Environment | 2012
Yele Sun; Zifa Wang; Huabin Dong; Ting Yang; Jie Li; Xiaole Pan; Ping Chen; John T. Jayne
Atmospheric Chemistry and Physics | 2011
Xiaole Pan; Yugo Kanaya; Z. F. Wang; Y. Liu; P. Pochanart; Hajime Akimoto; Youwen Sun; Huabin Dong; J. Li; Hitoshi Irie; Masayuki Takigawa
Atmospheric Chemistry and Physics | 2012
Huabin Dong; L. M. Zeng; Min Hu; Yusheng Wu; Y. Zhang; J. Slanina; Mei Zheng; Z. F. Wang; R. Jansen
Atmospheric Chemistry and Physics | 2016
Zhaofeng Tan; Hendrik Fuchs; Keding Lu; Andreas Hofzumahaus; Birger Bohn; Sebastian Broch; Huabin Dong; Sebastian Gomm; Rolf Häseler; Ling-Yan He; F. Holland; Xin Li; Ying Liu; Sihua Lu; Franz Rohrer; Min Shao; Baolin Wang; Ming Wang; Yusheng Wu; Limin Zeng; Yinsong Zhang; Andreas Wahner; Yuanhang Zhang