Contribution of evaporative emissions from gasoline vehicles toward total VOC emissions in Japan

2013 ◽  
Vol 449 ◽  
pp. 143-149 ◽  
Author(s):  
Hiroyuki Yamada
2015 ◽  
Vol 49 (21) ◽  
pp. 13067-13074 ◽  
Author(s):  
Ingrid J. George ◽  
Michael D. Hays ◽  
Jason S. Herrington ◽  
William Preston ◽  
Richard Snow ◽  
...  

2018 ◽  
Author(s):  
Congbo Song ◽  
Yan Liu ◽  
Shida Sun ◽  
Luna Sun ◽  
Yanjie Zhang ◽  
...  

Abstract. Vehicular emission is a key contributor to ambient volatile organic compounds (VOCs) and NOx in Chinese megacities. However, the information of real-world emission factors (EFs) for a typical urban fleet is still limited, hindering the development of a more reliable emission inventory in China. Based on a more-than-two-week (August 8–24, 2017) tunnel test in urban Tianjin in northern China, and on the use of a statistical regression model, the Positive Matrix Factorization (PMF) receptor model, and the Calculate Emissions from Road Transport (COPERT) IV model, characteristics of vehicular VOCs-NOx-CO emissions were analyzed systematically. The fleet-average EFs (pollutant: downslope, upslope, and overall in mg km−1 veh−1) were estimated respectively as follows: (NO: 61.92 ± 72.46, 158.58 ± 73.48, 97.52 ± 69.84), (NO2: 16.52 ± 11.49, 23.98 ± 20.14, 15.86 ± 9.38), (NOx: 79.45 ± 78.43, 181.22 ± 88.29, 116.56 ± 77.61), and (CO: 269.96 ± 342.38, 577.76 ± 382.22, 344.67 ± 250.01). The EFs of NO-NO2-NOx and CO from heavy-duty vehicles (or diesel vehicles) were differentiated from light-duty vehicles (or gasoline vehicles). The ratios (v / v) of NO2 to NOx in the primary vehicular exhaust were approximately 0.18 ± 0.09, 0.10 ± 0.22 and 0.10 ± 0.05 for downslope, upslope, and the entire tunnel, respectively. The fleet-average EF of the 99-target non-methane VOCs (NMVOCs) was 40.56 ± 12.18 mg km−1 veh−1, lower than the previous studies in China. The BTEX (benzene, toluene, ethylbenzene, p-xylene, m-xylene and o-xylene) levels decreased by approximately 79 % when emission standards increased from China I to China V. The source profiles of NMVOCs from the tailpipe and evaporative emissions were resolved by the PMF model. The evaporative emissions accounted for nearly one-half of the total vehicular VOC emissions, indicating that evaporative and tailpipe emissions contributed equally to VOC emissions. The relative contributions of evaporative NMVOC emissions to total vehicular NMVOC emissions are temperature-dependent with the average increasing ratio of 7.55 % °C−1. The primary emission ratio (ER, m / m) of VOCs / NOx was approximately 2.04, suggesting that vehicular NOx and VOCs can be co-emitted with a proper ER. According to the vehicular ERs of VOCs / NOx in Tianjin (2000–2016) and China (2010–2030), as even more stringent emission standards are implemented in the future, the O3 chemical regimes were likely to be VOCs-limited (i.e., 8 : 1 threshold) for cities or regions where VOCs and NOx emissions are dominated by vehicular exhaust. Our study enriched the database on the fleet-average emission factors of on-road vehicles for emission inventory, air quality modeling, and health effects studies, provided implications for following O3 control in China from the view of primary emission, and highlighted the importance of further control of evaporative emissions.


2015 ◽  
Vol 15 (6) ◽  
pp. 7977-8015 ◽  
Author(s):  
C. Huang ◽  
H. L. Wang ◽  
L. Li ◽  
Q. Wang ◽  
Q. Lu ◽  
...  

Abstract. VOC species from vehicle exhaust and gas evaporation were investigated by chassis dynamometer and on-road measurements of 9 gasoline vehicles, 7 diesel vehicles, 5 motorcycles, and 4 gas evaporation samples. The SOA mass yields of gasoline, diesel, motorcycle exhausts, and gas evaporation were calculated based on the mixing ratio of individual VOC species. The SOA mass yields of gasoline and motorcycle exhaust were similar to the results of the published smog chamber study with the exception of that of diesel exhaust was 20% lower than experimental data (Gordon et al., 2013, 2014a, b). This suggests the requirement for further research on SVOC or LVOC emissions. A vehicular emission inventory was compiled based on a local survey of vehicle mileage traveled and real-world measurements of vehicle emission factors. The inventory-based vehicular initial emission ratio of OA to CO was 15.6 μg m−3 ppmv−1. The OA production rate reached 22.3 and 42.7 μg m−3 ppmv−1 under high-NOx and low-NOx conditions, respectively. To determine the vehicular contribution to OA pollution, the inventory-based OA formation ratios for vehicles were calculated with a photochemical-age-based parameterization method and compared with the observation-based OA formation ratios in the urban atmosphere of Shanghai. The results indicated that VOC emissions from vehicle exhaust and gas evaporation only explained 15 and 22% of the total organic aerosols observed in summer and winter, respectively. SOA production only accounted for 25 and 18% of the total vehicular OA formation in summer and winter. VOC emissions from gasoline vehicles contribute 21–38% of vehicular OA formation after 6–24 h of photochemical aging. The results suggest that vehicle emissions are an important contributor to OA pollution in the urban atmosphere of Shanghai. However, a large number of OA mass in the atmosphere still cannot be explained in this study. SOA formation contributions from other sources (e.g. coal burning, biomass burning, cooking, dust, etc.) as well as IVOCs and SVOCs from the combustion sources need to be considered in future studies.


2018 ◽  
Vol 618 ◽  
pp. 1685-1691 ◽  
Author(s):  
Hiroo Hata ◽  
Hiroyuki Yamada ◽  
Kazuo Kokuryo ◽  
Megumi Okada ◽  
Chikage Funakubo ◽  
...  

2008 ◽  
Vol 3 (3) ◽  
pp. 14-20
Author(s):  
Sayavur I. Bakhtiyarov ◽  
◽  
Panakhov G.M ◽  
Eldar M. Abbasov ◽  
◽  
...  
Keyword(s):  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
M. Y. Song ◽  
H. Chun

AbstractVolatile organic compounds (VOCs) are secondary pollutant precursors having adverse impacts on the environment and human health. Although VOC emissions, their sources, and impacts have been investigated, the focus has been on large-scale industrial sources or indoor environments; studies on relatively small-scale enterprises (e.g., auto-repair workshops) are lacking. Here, we performed field VOC measurements for an auto-repair painting facility in Korea and analyzed the characteristics of VOCs emitted from the main painting workshop (top coat). The total VOC concentration was 5069–8058 ppb, and 24–35 species were detected. The VOCs were mainly identified as butyl acetate, toluene, ethylbenzene, and xylene compounds. VOC characteristics differed depending on the paint type. Butyl acetate had the highest concentration in both water- and oil-based paints; however, its concentration and proportion were higher in the former (3256 ppb, 65.5%) than in the latter (2449 ppb, 31.1%). Comparing VOC concentration before and after passing through adsorption systems, concentrations of most VOCs were lower at the outlets than the inlets of the adsorption systems, but were found to be high at the outlets in some workshops. These results provide a theoretical basis for developing effective VOC control systems and managing VOC emissions from auto-repair painting workshops.


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