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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 1,171 records · Page 65
All sourcesNASA NTRSDOE OSTI
DOE OSTI2012

Isothermal desulfation of pre-sulfated Pt-BaO/γ-Al2O3 lean NOx trap catalysts with H2: the effect of H2 concentration and the roles of CO2 and H2O

The desulfation mechanisms of pre-sulfated Pt-BaO/{gamma}-Al{sub 2}O{sub 3} lean NOx trap catalysts were investigated under isothermal conditions (600 C) using H{sub 2} as the reductant. Sulfates were found to be reduced first with H{sub 2} to produce SO{sub 2}, followed by a reaction between SO{sub 2} and H{sub 2} to produce H{sub 2}S. Gas analysis during the rich pulse reveals that the sulfur removal efficiency is initially proportional to the H{sub 2} concentration. At constant H{sub 2} concentration the overall desulfation efficiency decreases in the order of H{sub 2}/CO{sub 2}/H{sub 2}O > H{sub 2}/CO{sub 2} > H{sub 2}/H{sub 2}O > H{sub 2}, as confirmed by XPS analysis of residual sulfur in the desulfated samples. H{sub 2}O limits the evolution of SO{sub 2} at an early stage of the rich pulse and enhances the production of H{sub 2}S in later stages of reduction. CO{sub 2} is involved in both the formation of COS and the production of H{sub 2}O (via the reverse water-gas shift reaction), therefore, resulting in an increased overall efficiency.

54 ENVIRONMENTAL SCIENCES↗
DOE OSTI2018

Molecular structure and sour gas surface chemistry of supported K 2 O/WO 3 /Al 2 O 3 catalysts

Molecular structures of the unprompted and K 2 O-promoted supported WO 3 /Al 2 O 3 catalysts were studied with in situ Raman and UV-vis spectroscopy. In situ Raman spectra revealed that supported 20% WO 3 /Al 2 O 3 corresponds to near monolayer coverage of isolated and oligomeric surface WOx species on Al 2 O 3 . Above monolayer surface WO x coverage (21% WO 3 /Al 2 O 3 ), crystalline WO 3 nanoparticles are also present. The addition of K 2 O to the supported WO 3 /Al 2 O 3 catalyst increased the concentration of isolated surface WO x species and did not form K 2 WO 4 nanoparticles. The reducibility of the tungsten oxide structures depends on their structures (2D or 3D) and the K 2 O promoter. Their interaction with acidic CO 2 and SO 2 gases was also investigated. Adsorption of CO 2 creates several surface carbonate species of varying acidity that were detected using a combination of in situ IR and mass spectroscopy. Adsorbed bicarbonate form on weakly basic surface sites on tungsten oxide monolayer WO 3 /Al 2 O 3 catalyst as well as in the presence of low 2.5% K 2 O loading. At high 5% K 2 O loading, the presence of the strong surface basic sites yields adsorbed carbonates. In conclusion, after SO 2 pretreatment, however, new strongly adsorbed sulfate appears on the surface that inhibit CO 2 adsorption.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Effect of alumina incorporation on the sulfur tolerance of the dual-catalyst aftertreatment system for reduction of nitrogen oxides under lean conditions

Presence of sulfur or sulfur additives in natural gas lead to the formation of sulfur dioxide in the exhaust stream of natural gas-fired lean-burn engines. The sulfur tolerance and hydrothermal stability of the dual-catalyst aftertreatment system comprising a reduction catalyst (palladium supported on sulfated zirconia- Pd/SZ) and an oxidation catalyst (cobalt oxide supported on ceria- CoO x /CeO 2 ) for NOx reduction under lean-burn conditions has been tested under simulated engine exhaust conditions. Alumina-incorporated Pd/SZ (Pd/SZ(Alumina)) reduction catalyst as part of the dual catalyst bed demonstrated superior sulfur tolerance in the presence of 5 ppm SO 2 in the feed. The ratio of the reduction to oxidation catalyst was also seen to affect the hydrothermal stability under wet conditions with SO 2 in the reaction medium. The effect of hydrocarbon and water concentration in the reaction mixture on the sulfur tolerance of the dual-catalyst bed was studied. Increasing the reaction temperature from 450°C to 500°C demonstrated very stable NO x conversion and improved CH 4 conversions when the dual-catalyst bed was kept on-stream for 40 h -1 . X-ray photoelectron spectroscopy on samples poisoned with SO 2 ex-situ revealed the deposition of surface sulfates on the Pd/SZ catalyst samples and a combination of sulfates and sulfites on the CoO x /CeO 2 on treatment with SO 2 . The presence of alumina in the Pd/SZ sample protects the support from SO 2 poisoning as the oxidation state of the zirconia support remained largely unchanged on poisoning while in the CoO x /CeO 2 sample, sulfur poisoning likely affects the cerium redox cycle (Ce 3+ -Ce 4+ ). 27 Al magic angle spinning nuclear magnetic resonance (MAS NMR) revealed redistribution of the octahedral and tetrahedral Al-O coordination on SO 2 poisoning. Due to association with deposited sulfates on the catalyst, shielding effect on the Al nuclei resulted in an increased octahedral Al-O coordination in the poisoned sample.

03 NATURAL GAS↗
DOE OSTI2019

Solvent-free and one-pot synthesis of ultramicroporous carbons with ultrahigh nitrogen contents for sulfur dioxide capture

SO 2 from industrial tail gas is of great significance to control the environmental issues potentially induced by SO 2 emission. In the present work, porous carbons with rich ultramicropores and ultrahigh N contents (11.5–17.3 wt%) were synthesized by directly pyrolyzing the mixtures of glucose and urea at 700 °C, without the use of any solvents. Additionally, the synthesized porous carbons were characterized for porosity, morphology and elemental compositions, and also systematically investigated for SO 2 capture performance. Furthermore, it is found that the adsorption of SO 2 on synthesized porous carbons shows chemical behavior, owing to the strong acid-based interaction between SO 2 and pyridinic N. As consequence, the SO 2 capacities of synthesized porous carbons are very high, especially at low pressures (4.16 mmol/g at 296.2 K and 10 kPa). The synthesized porous carbons also display impressive adsorption selectivities for SO 2 /CO 2 /N 2 mixed gas, and good reversibility for SO 2 adsorption. Thus, it is believed that the synthesized porous carbons are promising candidates for selective and reversible SO 2 capture.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2026

Liquified SO 2 induced solid/cathode electrolyte interphase for lithium ion batteries

Formation of robust solid/cathode electrolyte interphases (S/CEI) is vital for long-term stability and high-performance operation of lithium-ion batteries (LIBs), particularly under high voltage regimes. However, engineering electrochemically stable S/CEIs that effectively suppress interfacial side reactions remains a key challenge. Herein, we introduce a liquefied sulfur dioxide (SO 2 )– ionic liquid complex as a fluorine-free multifunctional electrolyte additive for the first time that significantly improves the formation of sulfate/sulfite-rich S/CEI layers at both graphite and NMC811 interfaces. The unique SO 2 -N coordination with a 1,2,4-triazolide-based ionic liquid enables homogeneous SO 2 dissolution, resulting in controlled SO 2 decomposition during the initial electrochemical cycle. This decomposition yields sulfur-rich interphase species that stabilize the electrolyte-electrode interface, reduce impedance growth, and lessen electrolyte decomposition. Electrochemical tests show significantly improved cycle life, reduced polarization, and increased Coulombic efficiency for both anodes and cathodes. XPS confirms the presence of SO 2 -derived surface species that contribute to interfacial stability. In conclusion, this approach highlights a new direction for interphase engineering using liquefied gas additives and opens pathways for sulfur-based S/CEI chemistry in advanced battery systems.

Graphite↗
DOE OSTI2023

Electrochemical leaching of critical materials from lithium-ion batteries: A comparative life cycle assessment

The manufacturing of lithium-ion batteries (LIB) requires critical materials such as cobalt (Co) and lithium (Li) that are essential for clean-energy products including electric vehicles. Because of their rapidly increasing demand and limited supply, the recycle and reuse of these materials from end-of-life LIB have garnered a lot of interest. Electrochemical leaching has emerged as a sustainable method to extract critical materials out of LIBs, so life cycle assessment was conducted to compare the environmental impacts with traditional peroxide-based leaching and another emerging technology – SO 2 -based leaching. The results showed that electrochemical leaching reduces the global warming potential (GWP) by 80%-87% compared to peroxide-based leaching due to a lower acid consumption, avoidance of hydrogen peroxide, and regeneration of reducing agent iron (II) sulfate and compares well with SO 2 -based leaching in most impact categories. Furthermore, the analysis suggested renewable energy can further reduce the environment footprint of electrochemical leaching.

36 MATERIALS SCIENCE↗
DOE OSTI2012

Compact, DC-electrical biased sulfur dioxide sensing elements for use at high temperatures

Fabrication and operation of sensing elements for the detection of sulfur dioxide (SO_2) at high temperature (800 900 ^oC) is reported. The sensing elements consisted of three (two oxide and one Pt) electrodes on yttria-stabilized zirconia substrates. To operate the elements, a DC current (typically about 0.1 mA) is driven between two of the electrodes and the voltage between one of these electrodes and the third electrode is used as the sensing signal. These sensing elements respond very strongly to SO_2, for example 2 ppm_V of SO_2 in a background of 7 vol% O_2, balance N_2 was found to produce a >10% change in the sensing signal, which could be easily detected. Sensing elements fabricated to be nominally identical were shown to yield qualitatively identical sensing behavior, and temperature, oxygen content, and flow were all found to strongly impact sensing performance. The impact of interferents, such as NO_x and CO, was evaluated and found to be relatively small in comparison to the SO_2 response. The sensing response, over a 1 month period, was very stable, with the ratio of the average change in sensing signal over one day to the average sensing signal magnitude being about 0.1%.

36 MATERIALS SCIENCE↗
DOE OSTI2023

Evaluation of Uncertainties in the Anthropogenic SO 2 Emissions in the USA from the OMI Point Source Catalog

Satellite remote sensing is a promising method of monitoring emissions that may be missing in inventories, but the accuracy of these estimates is often not clear. We demonstrate here a comprehensive evaluation of errors in anthropogenic sulfur dioxide (SO 2 ) emission estimates from NASA’s OMI point source catalog for the contiguous US by comparing emissions from the catalog with high-quality emission inventory data over different dimensions including size of individual sources, aggregate vs individual source errors, and potential bias in individual source estimates over time. For sources that are included in the catalog, we find that errors in aggregate (sum of error for all included sources) are relatively low. Errors for individual sources in any given year can be substantial, however, with over- or underestimates in terms of total error ranging from –80 to 110 kt (roughly 10–90th percentile). In this study, we find that these errors are not necessarily random over time and that there can be consistently positive or negative biases for individual sources. We did not find any overall statistical relationship between the degree of isolation of a source and bias, either at a 40 or 70 km scales. For a sub-set of sources where inventory emissions over a radius of 70 km around an OMI detection are larger than twice the emissions within 40 km, the OMI value is consistently overestimated. We find, as expected, that emission sources not included in the catalog are the largest aggregate source of difference between the satellite estimates and inventories, especially in more recent years where source emission magnitudes have been decreasing and note that trends in satellite detections do not necessarily track trends in total emissions. We find that the OMI-based SO 2 emissions are accurate in aggregate, when summed over a number of sources, but must be interpreted more cautiously at the individual source level. Similar analyses would be valuable for other satellite emission estimates; however, in many cases, the appropriate high-quality reference data may need to be generated.

54 ENVIRONMENTAL SCIENCES↗
DOE OSTI2016

The rotation-vibration structure of the SO 2 C 1 B 2 state explained by a new internal coordinate force field

A new quartic force field for the SO 2 C ~ 1 B 2 state has been derived, based on high resolution data from S 16 O 2 and S 18 O 2 . Included are eight b 2 symmetry vibrational levels of S 16 O 2 reported in the first paper of this series [G. B. Park, et al., J. Chem. Phys. 144, 144311 (2016)]. Many of the experimental observables not included in the fit, such as the Franck-Condon intensities and the Coriolis-perturbed effective C rotational constants of highly anharmonic C ~ state vibrational levels, are well reproduced using our force field. Because the two stretching modes of the C ~ state are strongly coupled via Fermi-133 interaction, the vibrational structure of the C state is analyzed in a Fermi-system basis set, constructed explicitly in this work via partial diagonalization of the vibrational Hamiltonian. The physical significance of the Fermi-system basis is discussed in terms of semiclassical dynamics, based on study of Fermi-resonance systems by Kellman and coworkers [M. E. Kellman and L. Xiao, J. Chem. Phys. 93, 5821 (1990)]. By diagonalizing the vibrational Hamiltonian in the Fermi-system basis, the vibrational characters of all vibrational levels can be determined unambiguously. It is shown that the bending mode cannot be treated separately from the coupled stretching modes, particularly at vibrational energies of more than 2000 cm –1 . Based on our force field, the structure of the Coriolis interactions in the C ~ state of SO 2 is also discussed. As a result, we identify the origin of the alternating patterns in the effective C rotational constants of levels in the vibrational progressions of the symmetry-breaking mode, ν β (which correlates with the antisymmetric stretching mode in our assignment scheme).

74 ATOMIC AND MOLECULAR PHYSICS↗
DOE OSTI2016

The effect of environment on thermal barrier coating lifetime

While the water vapor content of the combustion gas in natural gas-fired land-based turbines is ~10%, it can be 20–85% with coal-derived (syngas or H 2 ) fuels or innovative turbine concepts for more efficient carbon capture. Additional concepts envisage working fluids with high CO 2 contents to facilitate carbon capture and sequestration. To investigate the effects of changes in the gas composition on thermal barrier coating (TBC) lifetime, furnace cycling tests (1-h and 100-h cycles) were performed in air with 10, 50, and 90 vol. % water vapor and CO 2 -10% H 2 O and compared to prior results in dry air or O 2 . Two types of TBCs were investigated: (1) diffusion bond coatings (Pt-diffusion or Pt-modified aluminide) with commercial electron-beam physical vapor-deposited yttria-stabilized zirconia (YSZ) top coatings on second-generation superalloy N5 and N515 substrates and (2) high-velocity oxygen fuel (HVOF) sprayed MCrAlYHfSi bond coatings with air plasma-sprayed YSZ top coatings on superalloys X4, 1483, or 247 substrates. For both types of coatings exposed in 1-h cycles, the addition of water vapor resulted in a decrease in coating lifetime, except for Pt-diffusion coatings which were unaffected by the environment. In 100-h cycles, environment was less critical, perhaps because coating failure was chemical (i.e., due to interdiffusion) rather than mechanical. As a result, in both 1-h and 100-h cycles, CO 2 did not appear to have any negative effect on coating lifetime.

36 MATERIALS SCIENCE↗
DOE OSTI2016

On the Path to SunShot. The Environmental and Public Health Benefits of Achieving High Solar Penetrations in the United States

Compared with fossil fuel generators, photovoltaics (PV) and concentrating solar power (CSP) produce far lower lifecycle levels of greenhouse gas (GHG) emissions and harmful pollutants including fine particular matter (PM2.5), sulfur dioxide (SO 2 ), and nitrogen oxides (NO x ). In this report, we monetize the emission reductions from achieving the U.S. Department of Energy's SunShot deployment goals: 14% of U.S. electricity demand met by solar in 2030 and 27% in 2050. We estimate that achieving these goals could reduce cumulative power-sector GHG emissions by 10% between 2015 and 2050, resulting in savings of $238-$252 billion. This is equivalent to 2.0-2.2 cents per kilowatt-hour of solar installed (cents/kWh-solar). Similarly, realizing these levels of solar deployment could reduce cumulative power-sector emissions of PM2.5 by 8%, SO 2 by 9%, and NOx by 11% between 2015 and 2050. This could produce $167 billion in savings from lower future health and environmental damages, or 1.4 cents/kWh-solar--while also preventing 25,000-59,000 premature deaths. To put this in perspective, this estimated combined benefit of 3.5 cents/kWh-solar due to SunShot-level solar deployment is approximately equal to the additional levelized cost of electricity reduction needed to make unsubsidized utility-scale solar competitive with conventional generators today. In addition, the analysis shows that achieving the SunShot goals could save 4% of total power-sector water withdrawals and 9% of total power-sector water consumption over the 2015-2050 period--a particularly important consideration for arid states where substantial solar will be deployed. These results have potential implications for policy innovation and the economic competitiveness of solar and other generation technologies.

14 SOLAR ENERGY↗
DOE OSTI2019

Oil‐Free, High-Temperature Heat Transfer Fluid Circulator

A high temperature Heat Transfer Fluid circulator compressor with wide turn down ratio aerodynamic performance was designed, fabricated and tested for application with high pressure super Critical CO2 fluid capable of temperatures and pressures to >750°C and 25 MPa respectively. The modular system decoupled the drive motor system from an independent compressor shaft to provide thermal isolation between the high temperature compressor shaft and the lower temperature capable motor elements. While the thermal management approach appears to be viable there are potential losses in the secondary cooling flows that need to be taken into account and fine-tuned during operation in order to achieve desired overall system efficiencies. The system was also shown to be viable and dynamically stable throughout the entire operating speed range, thereby validating the overall system configuration and structural design approach used. Finally, while it was not possible to achieve specific PTC-10 test points, the compressor performance tests provide sufficient data to indicate that the compressor has the ability to achieve the required performance in practice. The two key factors affecting compressor design and cost are the maximum expected temperature and pressure. The maximum allowable temperatures for current state-of-the-art (SOA) motor driven compressor technology is limited to of approximately 150-200°C, but inlet temperatures >750 °C may be encountered. While the optimal efficiency of compression is in the transcritical region, some concepts require inlet pressures to 225 bar.

14 SOLAR ENERGY↗
DOE OSTI2020

High-Temperature Heat Transfer Fluid Circulator for Concentrating Solar Power Systems

A high temperature Heat Transfer Fluid circulator compressor with wide turn down ratio aerodynamic performance was designed, fabricated and tested for application with high pressure super Critical CO2 fluid capable of temperatures and pressures to >750°C and 25 MPa respectively. The modular system decoupled the drive motor system from an independent compressor shaft to provide thermal isolation between the high temperature compressor shaft and the lower temperature capable motor elements. While the thermal management approach appears to be viable there are potential losses in the secondary cooling flows that need to be taken into account and fine-tuned during operation in order to achieve desired overall system efficiencies. The system was also shown to be viable and dynamically stable throughout the entire operating speed range, thereby validating the overall system configuration and structural design approach used. Finally, while it was not possible to achieve specific PTC-10 test points, the compressor performance tests provide sufficient data to indicate that the compressor has the ability to achieve the required performance in practice. The two key factors affecting compressor design and cost are the maximum expected temperature and pressure. The maximum allowable temperatures for current state-of-the-art (SOA) motor driven compressor technology is limited to of approximately 150-200°C, but inlet temperatures >750 °C may be encountered. While the optimal efficiency of compression is in the transcritical region, some concepts require inlet pressures to 225 bar.

14 SOLAR ENERGY↗
DOE OSTI2026

Biochemical Conversion of Herbaceous Biomass to Renewable Diesel: Biorefinery Marginal Air Quality Impacts and Comparison to Feedstock Production

This study assesses the air quality impacts of an advanced biorefinery that produces renewable diesel blendstock (RDB) from lignocellulosic biomass via aerobic respiration (Davis et al. 2022) by estimating fine particulate matter (PM2.5) impacts from biorefinery emissions. It continues a prior analysis that used a geospatial assessment to identify source regions for biomass feedstocks and studied the impact of feedstock production emissions on air quality (Thind et al. 2022). Thind et al. (2022) identified RDB biorefineries that can use corn stover feedstocks of 2,000; 5,200; and 9,100 dry metric tons per day (DMT/day), based in Iowa, and suggested 7 unique counties can serve as hosts for a biorefinery that draws biomass feedstock from neighboring counties. Given 13 unique county-biorefinery size combinations and two waste lignin end uses at the biorefinery (lignin as a fuel for electricity generation and lignin for pellet production), the air-quality-related sustainability aspects of each of these 26 scenarios are assessed by estimating the annual average impacts of biorefinery emissions on the dispersion and formation of secondary PM2.5 in the atmosphere using a novel reduced-complexity air quality model called the Intervention Model for Air Pollution (InMAP). The 26 biorefinery design combinations help capture how a biorefinery's emissions of air pollutants and their resulting impact on local and regional air quality are influenced by the magnitude of production scale, lignin utilization strategy, and location of a proposed biorefinery. Methods developed in Thind et al. (2022) are applied to estimate the constraints on primary PM2.5 and secondary PM2.5 precursor emissions based on compliance with U.S. Environmental Protection Agency's (EPA's) annual primary National Ambient Air Quality Standard (NAAQS) of PM2.5 (i.e.12.0 micrograms per cubic meter (microgram/m3)) at downwind receptors of a biorefinery. Incremental PM2.5 concentrations caused by the emission of biorefining corn stover into RDB are assessed and compared to those of corn stover production. To illuminate which upstream supply chain stage of renewable diesel production contributes most to air quality impacts, marginal PM2.5 concentrations are compared between both stages at multiple downwind air quality monitor locations. In addition, through a hotspot analysis, we identify the primary contributing factors of emissions within the feedstock production and biorefinery stage operations. In doing so, we provide insights for improving the air pollutant emission-related sustainability of advanced lignocellulosic biofuel production.

09 BIOMASS FUELS↗
DOE OSTI2023

Updating and Evaluating Anthropogenic Emissions for NOAA’s Global Ensemble Forecast Systems for Aerosols (GEFS-Aerosols): Application of an SO 2 Bias-Scaling Method

We updated the anthropogenic emissions inventory in NOAA’s operational Global Ensemble Forecast for Aerosols (GEFS-Aerosols) to improve the model’s prediction of aerosol optical depth (AOD). We used a methodology to quickly update the pivotal global anthropogenic sulfur dioxide (SO 2 ) emissions using a speciated AOD bias-scaling method. The AOD bias-scaling method is based on the latest model predictions compared to NASA’s Modern-Era Retrospective analysis for Research and Applications, version 2 (MERRA2). The model bias was subsequently applied to the CEDS 2019 SO 2 emissions for adjustment. The monthly mean GEFS-Aerosols AOD predictions were evaluated against a suite of satellite observations (e.g., MISR, VIIRS, and MODIS), ground-based AERONET observations, and the International Cooperative for Aerosol Prediction (ICAP) ensemble results. The results show that transitioning from CEDS 2014 to CEDS 2019 emissions data led to a significant improvement in the operational GEFS-Aerosols model performance, and applying the bias-scaled SO 2 emissions could further improve global AOD distributions. The biases of the simulated AODs against the observed AODs varied with observation type and seasons by a factor of 3~13 and 2~10, respectively. The global AOD distributions showed that the differences in the simulations against ICAP, MISR, VIIRS, and MODIS were the largest in March–May (MAM) and the smallest in December–February (DJF). When evaluating against the ground-truth AERONET data, the bias-scaling methods improved the global seasonal correlation (r), Index of Agreement (IOA), and mean biases, except for the MAM season, when the negative regional biases were exacerbated compared to the positive regional biases. The effect of bias-scaling had the most beneficial impact on model performance in the regions dominated by anthropogenic emissions, such as East Asia. However, it showed less improvement in other areas impacted by the greater relative transport of natural emissions sources, such as India. The accuracies of the reference observation or assimilation data for the adjusted inputs and the model physics for outputs, and the selection of regions with less seasonal emissions of natural aerosols determine the success of the bias-scaling methods. A companion study on emission scaling of anthropogenic absorbing aerosols needs further improved aerosol prediction.

54 ENVIRONMENTAL SCIENCES↗
DOE OSTI2024

Long-Term Dynamics of Atmospheric Sulfur Dioxide in Urban and Rural Regions of China: Urbanization and Policy Impacts

High levels of sulfur dioxide (SO 2 ) due to human activities pose a serious air pollution issue in China, especially in urban agglomerations. However, limited research has investigated the impact of anthropogenic emissions on higher SO 2 concentrations in urban regions compared to rural areas in China. Here, we analyzed the trends in SO 2 concentrations from 1980 to 2021 in China using the Modern-Era Retrospective Analysis for Research and Applications, version 2 (MERRA-2) dataset. SO 2 column concentrations from the Copernicus Atmosphere Monitoring Service (CAMS) and the Ozone Monitoring Instrument (OMI) during the years 2007–2021 were also examined for validation and comparison purposes. Eight representative areas, including four urban regions (Pearl River Delta [PRD], Beijing-Tianjin-Hebei [BTH], Yangtze River Delta [YRD], and Sichuan Basin [SCB]) and four rural regions (Northeast Region [NER], Mongolian Region [MR], West Region [WR], and Tibetan Plateau Region [TR]) were selected for the analysis. Overall, a significant but fluctuating increase in SO 2 concentrations over China was observed during 1980–2021. During 1980–1997 and 2000–2010, there was an increase in SO 2 concentration, while during 1997–2000 and 2010–2021, a decreasing trend was observed. The average increase in SO 2 concentration was approximately 16 times higher in urban regions than in the rural background. We also found that SO 2 dynamics were highly associated with expansion of urban areas, population density, and gross domestic product. Nonetheless, since 2007, SO 2 concentrations have exhibited a downward trend, which is mainly attributed to the air pollution policies implemented by the Chinese government. Our findings highlight the need for further studies on the impact of SO 2 on regional climate change in China.

54 ENVIRONMENTAL SCIENCES↗
DOE OSTI2021

aosso2.b1

Harmonized (some QC added) aosso2 datastream

54 ENVIRONMENTAL SCIENCES↗