Estimation and Uncertainty Analysis of Secondary Organic Carbon Using 1 Year of Hourly Organic and Elemental Carbon Data

2019 ◽  
Vol 124 (5) ◽  
pp. 2774-2795 ◽  
Author(s):  
Cheng Wu ◽  
Dui Wu ◽  
Jian Zhen Yu
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Yan Cheng ◽  
Judith C. Chow ◽  
John G. Watson ◽  
Jiamao Zhou ◽  
Suixin Liu ◽  
...  

AbstractCarbonaceous aerosols were characterized in 19 Chinese cities during winter and summer of 2013. Measurements of organic carbon (OC) and elemental carbon (EC) levels were compared with those from 14 corresponding cities sampled in 2003 to evaluate effects of emission changes over a decade. Average winter and summer OC and EC decreased by 32% and 17%, respectively, from 2003 to 2013, corresponding to nationwide emission control policies implemented since 2006. The extent of carbon reduction varied by season and by location. Larger reductions were found for secondary organic carbon (SOC, 49%) than primary organic carbon (POC, 25%). PM2.5 mass and total carbon concentrations were three to four times higher during winter than summer especially in the northern cities that use coal combustion for heating.


2014 ◽  
Vol 468-469 ◽  
pp. 1103-1111 ◽  
Author(s):  
Yuan Cheng ◽  
Ke-bin He ◽  
Feng-kui Duan ◽  
Zhen-yu Du ◽  
Mei Zheng ◽  
...  

2014 ◽  
Vol 7 (1) ◽  
pp. 131-169 ◽  
Author(s):  
U. Dusek ◽  
M. Monaco ◽  
M. Prokopiou ◽  
F. Gongriep ◽  
R. Hitzenberger ◽  
...  

Abstract. We thoroughly characterized a system for thermal separation of organic carbon (OC) and elemental carbon (EC) for subsequent radiocarbon analysis. Different organic compounds as well as ambient aerosol filter samples were introduced into an oven system and combusted to CO2 in pure O2. The main objective was to test which combustion times and temperatures are best suited to separate OC and EC. The final separation step for OC was combustion at 360 °C for 15 min. Combustion at this temperature proved enough to remove several organic test substances from the filter (including high molecular weight humic acid) but did not remove substantial amounts of EC. For isolation of EC, OC first needs to be completely removed from the filter. This was achieved by water extraction of the filter, followed by combustion of the water insoluble OC at 360 °C and combustion at an intermediate temperature step of 2 min at 450 °C. This last step removed the most refractory OC together with some EC. Finally, the remaining EC was combusted to CO2 at 650 °C. The recovery of black carbon after the intermediate 450 °C step was approximately 80%. Several tests provided strong evidence that OC was removed efficiently during the intermediate temperature step: (i) brown carbon, indicative of refractory OC, was removed; (ii) the fraction modern of EC did not decrease significantly if the temperature of the intermediate step was further increased. Based on tests with various organic compounds, we estimated that charred organic carbon could contribute 4–8% to an elemental carbon sample that was isolated according to our method.


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