scholarly journals Dramatic increase in reactive volatile organic compound (VOC) emissions from ships at berth after implementing the fuel switch policy in the Pearl River Delta Emission Control Area

2020 ◽  
Vol 20 (4) ◽  
pp. 1887-1900 ◽  
Author(s):  
Zhenfeng Wu ◽  
Yanli Zhang ◽  
Junjie He ◽  
Hongzhan Chen ◽  
Xueliang Huang ◽  
...  

Abstract. Limiting fuel sulfur content (FSC) is a widely adopted approach for reducing ship emissions of sulfur dioxide (SO2) and particulate matter (PM), particularly in emission control areas (ECAs), but its impact on the emissions of volatile organic compounds (VOCs) is still not well understood. In this study, emissions from ships at berth in Guangzhou, southern China, were characterized before and after the implementation of the fuel switch policy (IFSP) with an FSC limit of 0.5 % in the Pearl River Delta ECA (ECA-PRD). After IFSP, the emission factors (EFs) of SO2 and PM2.5 for the coastal vessels decreased by 78 % and 56 % on average, respectively; however, the EFs of the VOCs were 1807±1746 mg kg−1, approximately 15 times that of 118±56.1 mg kg−1 before IFSP. This dramatic increase in the emissions of the VOCs might have been largely due to the replacement of high-sulfur residual fuel oil with low-sulfur diesel or heavy oils, which are typically richer in short-chain hydrocarbons. Moreover, reactive alkenes surpassed alkanes to become the dominant group among the VOCs, and low-carbon-number VOCs, such as ethylene, propene and isobutane, became the dominant species after IFSP. As a result of the largely elevated EFs of the reactive alkenes and aromatics after IFSP, the emitted VOCs per kilogram of fuel burned had nearly 29 times greater ozone formation potential (OFP) and approximately 2 times greater secondary organic aerosol formation potential (SOAFP) than those before IFSP. Unlike the coastal vessels, the river vessels in the region used diesel fuels consistently and were not affected by the fuel switch policy, but the EFs of their VOCs were 90 % greater than those of the coastal vessels after IFSP, with approximately 120 % greater fuel-based OFP and 70 %–140 % greater SOAFP. The results from this study suggest that while the fuel switch policy could effectively reduce SO2 and PM emissions, and thus help control PM2.5 pollution, it will also lead to greater emissions of reactive VOCs, which may threaten ozone pollution control in harbor cities. This change for coastal or ocean-going vessels, in addition to the large amounts of reactive VOCs from the river vessels, raises regulatory concerns for ship emissions of reactive VOCs.

2019 ◽  
Author(s):  
Zhenfeng Wu ◽  
Yanli Zhang ◽  
Junjie He ◽  
Hongzhan Chen ◽  
Xueliang Huang ◽  
...  

Abstract. Limiting the fuel sulfur content (FSC) is a widely adopted approach to reduce ship emissions of sulfur dioxide (SO2) and particulate matters (PM) particularly in emission control areas (ECA), but its impact on the emission of volatile organic compounds (VOCs) is still not well understood. In this study, emissions from ships at berth in Guangzhou, south China, were characterized before and after implementing the fuel switch policy with a FSC limit of 0.5 % in the Pearl River Delta ECA in south China. After implementing the fuel switch policy, the emission factors (EFs) of SO2 and PM2.5 for coastal vessels dropped by 78 % and 56 % on average, respectively; the EFs of non-methane hydrocarbons (NMHCs), however, reached 1807 ± 1746 mg/kg, about 15 times that of 118 ± 56.1 mg/kg before implementing the new policy. This dramatic increase in the emission of NMHCs might be largely due to the replacement of high-sulfur residual fuel oil with low-sulfur diesel or heavy oils, which are typically more rich in short-chain hydrocarbons. Moreover, reactive alkenes overtook alkanes to become the dominant group among NMHCs and low carbon number NMHCs, such as ethylene, propene and isobutane, became the dominant species after the new policy. As a result of the largely elevated EFs of reactive alkenes and aromatics after the new policy, for per kilogram of fuel burned, emitted NMHCs had nearly 29 times larger ozone formation potentials (OFPs) and about 2 times higher secondary organic aerosol formation potentials (SOAFPs). Unlike coastal vessels, river vessels in the region used diesel fuels all along and were not affected by the fuel switch policy, but their EFs of NMHCs were even 90 % larger than that of coastal vessels after implementing the new policy, with about 120 % larger fuel-based OFPs and 70–140 % larger SOAFPs. The results from this study suggest that while the fuel switch policy could effectively reduce SO2 and PM emissions and thus help combat PM2.5 pollution, it would also lead to greater emissions of reactive VOCs, that may threatens ozone pollution control in the harbor cities. This change for coastal or ocean-going vessels, along with the large amounts of reactive VOCs from river vessels, raises regulatory concerns for ship emissions of reactive VOCs.


2016 ◽  
Author(s):  
Christopher Chan Miller ◽  
Daniel J. Jacob ◽  
Gonzalo González Abad ◽  
Kelly Chance

Abstract. The Pearl River Delta (PRD) is a densely populated hub of industrial activity located in southern China. OMI satellite observations reveal a large hotspot of glyoxal (CHOCHO) over the PRD that is almost twice as large as any other in Asia. Formaldehyde (HCHO) and NO2 observed by OMI are also high in the PRD but no more than in other urban/industrial areas of China. The CHOCHO hotspot in the PRD can be explained by industrial paint and solvent emissions of aromatic volatile organic compounds (VOCs), with toluene being a dominant contributor. By contrast, HCHO in the PRD originates mostly from VOCs emitted by combustion (principally vehicles). By applying a plume transport model to wind-segregated OMI data, we show that the CHOCHO and HCHO enhancements over the PRD observed by OMI are consistent with current VOC emission inventories. Prior work using CHOCHO retrievals from the SCIAMACHY satellite instrument suggested that aromatic VOC emissions in the PRD were too low by a factor of 10-20; we attribute this result in part to bias in the SCIAMACHY data and in part to underestimated CHOCHO yields from oxidation of aromatics. Our work points to the importance of better understanding CHOCHO yields from the oxidation of aromatics in order to interpret CHOCHO observations from space.


2015 ◽  
Vol 15 (22) ◽  
pp. 33583-33629 ◽  
Author(s):  
N. Li ◽  
T.-M. Fu ◽  
J. J. Cao ◽  
J. Y. Zheng ◽  
Q. Y. He ◽  
...  

Abstract. We simulated elemental carbon (EC) and organic carbon (OC) aerosols over the Pearl River Delta (PRD) area of China and compared the results to seasonal surface measurements, with the aim of quantifying carbonaceous aerosol sources from a "top-down" perspective. Our regional model was driven by current-best estimates of PRD EC (39.5 Gg C yr−1) and OC (32.8 Gg C yr−1) emissions and included updated secondary organic aerosol formation pathways. The simulated annual mean EC and OC concentrations were 4.0 and 7.7 μg C m−3, respectively, lower than the observed annual mean EC and OC concentrations (4.5 and 13.1 μg C m−3, respectively). We used multiple regression to match the simulated EC against seasonal mean observations. The resulting top-down estimate for EC emission in the PRD area was 52.9 ± 8.0 Gg C yr−1. We estimated the OC emission in the PRD area to be 60.2 ± 10.3 Gg C yr−1, based on the top-down EC emission estimate and the primary OC / EC ratios derived from bottom-up statistics. Using these top-down emission estimates, the simulated average annual mean EC and OC concentrations were improved to 4.4 and 9.5 μg C m−3, respectively, closer to the observations. Secondary sources accounted for 42 % of annual mean surface OC in our top-down simulations, with biogenic VOCs being the most important precursors.


2016 ◽  
Vol 16 (7) ◽  
pp. 4631-4639 ◽  
Author(s):  
Christopher Chan Miller ◽  
Daniel J. Jacob ◽  
Gonzalo González Abad ◽  
Kelly Chance

Abstract. The Pearl River delta (PRD) is a densely populated hub of industrial activity located in southern China. OMI (Ozone Monitoring Instrument) satellite observations reveal a large hotspot of glyoxal (CHOCHO) over the PRD that is almost twice as large as any other in Asia. Formaldehyde (HCHO) and NO2 observed by OMI are also high in the PRD but no more than in other urban/industrial areas of China. The CHOCHO hotspot over the PRD can be explained by industrial paint and solvent emissions of aromatic volatile organic compounds (VOCs), with toluene being a dominant contributor. By contrast, HCHO in the PRD originates mostly from VOCs emitted by combustion (principally vehicles). By applying a plume transport model to wind-segregated OMI data, we show that the CHOCHO and HCHO enhancements over the PRD observed by OMI are consistent with current VOC emission inventories. Prior work using CHOCHO retrievals from the SCIAMACHY satellite instrument suggested that emission inventories for aromatic VOCs in the PRD were too low by a factor of 10–20; we attribute this result in part to bias in the SCIAMACHY data and in part to underestimated CHOCHO yields from oxidation of aromatics. Our work points to the importance of better understanding CHOCHO yields from the oxidation of aromatics in order to interpret space-based CHOCHO observations in polluted environments.


Atmosphere ◽  
2021 ◽  
Vol 13 (1) ◽  
pp. 9
Author(s):  
Weiqiang Yang ◽  
Qingqing Yu ◽  
Chenglei Pei ◽  
Chenghao Liao ◽  
Jianjun Liu ◽  
...  

Volatile organic compounds (VOCs) are important precursors of photochemical ozone and secondary organic aerosol (SOA). Here, hourly variations of ambient VOCs were monitored with an online system at an urban site (Panyu, PY) in the Pearl River Delta region during August–September of 2020 in order to identify reactive VOC species and major sources of VOCs, OH loss rate (LOH), SOA formation potential (SOAFP), and corresponding emission source regions. The average concentration of VOCs at PY was 31.80 ± 20.82 ppbv during the campaign. The C2–C5 alkanes, aromatics, and ≥C6 alkanes contributed for the majority of VOC, alkenes and aromatics showed the highest contribution to LOH and SOAFP. Further, m/p-xylene, propene, and toluene were found to be the top three most reactive anthropogenic VOC species, with respective contributions of 11.6%, 6.1%, and 5.8% to total LOH. Toluene, m/p-xylene, and o-xylene constituted a large fraction of calculated SOAFP. Seven major sources were identified by using positive matrix factorization model. Vehicle exhaust made the most significant contribution to VOCs, followed by liquefied petroleum gas and combustion sources. However, industrial-related sources (including industrial solvent use and industrial process emission) had the largest contribution to LOH and SOAFP. By combining source contribution with wind direction and wind speed, the regions of different sources were further identified. Based on high-resolution observation data during ozone pollution, this study clearly exhibits key reactive VOC species and the major emission regions of different VOC sources, and thus benefits the accurate emission control of VOCs in the near future.


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