ABSTRACT
This study investigated the spatiotemporal variabilities in nitrogen dioxide (NO2), formaldehyde (HCHO), ozone (O3), and light-absorbing aerosols within the Greater Tokyo Area, Japan, which is the most populous metropolitan area in the world. The analysis is based on total tropospheric column, partial tropospheric column (within the boundary layer), and in situ observations retrieved from multiple platforms as well as additional information obtained from reanalysis and box model simulations. This study mainly covers the 2013–2020 period, focusing on 2020 when air quality was influenced by the coronavirus 2019 (COVID-19) pandemic. Although total and partial tropospheric NO2 columns were reduced by an average of about 10 % in 2020, reductions exceeding 40 % occurred in some areas during the pandemic state of emergency. Light-absorbing aerosol levels within the boundary layer were also reduced for most of 2020, while smaller fluctuations in HCHO and O3 were observed. The significantly enhanced degree of weekly cycling of NO2, HCHO, and light-absorbing aerosol found in urban areas during 2020 suggests that, in contrast to other countries, mobility in Japan also dropped on weekends. We conclude that, despite the lack of strict mobility restrictions in Japan, widespread adherence to recommendations designed to limit the COVID-19 spread resulted in unique air quality improvements.
ABSTRACT
The interaction of electromagnetic (EM) waves with the COVID-19 virus is studied to define the frequencies that cause maximum energy absorption by the virus and the power level needed to cause a lethal temperature rise. The full-wave EM simulator is used to model the virus and study the effects of its size and dielectric properties on the absorbed power across a wide range of frequencies. The results confirm potential resonance conditions, where specific frequencies produce maximum absorption and subsequent temperature rise that can destroy the virus. Furthermore, the study confirms that maximum power deposition in the virus occurs at specific wavelengths depending on its size. Also, the simulation is used to find the power required to destroy the virus and determine the total power required to destroy it in an oral activity, such as coughing, made by infected individuals. Furthermore, the study explained why irradiation by UV-C band is effective to decrease virus activity or even eradicate it.
ABSTRACT
Black carbon (BC) is recognized as the most important warming agent among atmospheric aerosol particles. The absorption efficiency of pure BC is rather well-known, nevertheless the mixing of BC with other aerosol particles can enhance the BC light absorption efficiency, thus directly affecting Earth's radiative balance. The effects on climate of the BC absorption enhancement due to the mixing with these aerosols are not yet well constrained because these effects depend on the availability of material for mixing with BC, thus creating regional variations.Here we present the mass absorption cross-section (MAC) and absorption enhancement of BC particles (Eabs), at different wavelengths (from 370 to 880 nm for online measurements and at 637 nm for offline measurements) measured at two sites in the western Mediterranean, namely Barcelona (BCN;urban background) and Montseny (MSY;regional background). The Eabs values ranged between 1.24 and 1.51 at the urban station, depending on the season and wavelength used as well as on the pure BC MAC used as a reference. The largest contribution to Eabs was due to the internal mixing of BC particles with other aerosol compounds, on average between a 91 % and a 100 % at 370 and 880 nm, respectively. Additionally, 14.5 % and 4.6 % of the total enhancement at the short ultraviolet (UV) wavelength (370 nm) was due to externally mixed brown carbon (BrC) particles during the cold and the warm period, respectively. On average, at the MSY station, a higher Eabs value was observed (1.83 at 637 nm) compared to BCN (1.37 at 637 nm), which was associated with the higher fraction of organic aerosols (OA) available for BC coating at the regional station, as denoted by the higher organic carbon to elemental carbon (OC:EC) ratio observed at MSY compared to BCN. At both BCN and MSY, Eabs showed an exponential increase with the amount of non-refractory (NR) material available for coating (RNR-PM). The Eabs at 637 nm at the MSY regional station reached values up to 3 during episodes with high RNR-PM, whereas in BCN, Eabs kept values lower than 2 due to the lower relative amount of coating materials measured at BCN compared to MSY. The main sources of OA influencing Eabs throughout the year were hydrocarbon OA (HOA) and cooking-related OA (COA), i.e. primary OA (POA) from traffic and cooking emissions, respectively, at both 370 and 880 nm. At the short UV wavelength (370 nm), a strong contribution to Eabs from biomass burning OA (BBOA) and less oxidized oxygenated OA (LO-OOA) sources was observed in the colder period. Moreover, we found an increase of Eabs with the ageing state of the particles, especially during the colder period. This increase of Eabs with particle ageing was associated with a larger relative amount of secondary OA (SOA) compared to POA. The availability of a long dataset at both stations from offline measurements enabled a decade-long trend analysis of Eabs at 637 nm, that showed statistically significant (s.s.) positive trends of Eabs during the warmer months at the MSY station. This s.s. positive trend in MSY mirrored the observed increase of the OC:EC ratio over time. Moreover, in BCN during the COVID-19 lockdown period in spring 2020 we observed a sharp increase of Eabs due to the observed sharp increase of the OC:EC ratio. Our results show similar values of Eabs to those found in the literature for similar background stations.
ABSTRACT
The COVID-19 epidemic-led lockdown (LD) from March 25 to May 31, 2020, had a different level of impact on air quality in the ecologically sensitive region of northeast India, even though the restriction on main anthropogenic activities was expected to reduce particulate matter concentration. The daily average black carbon concentration measured at 880 nm (BC880) was 1.5–15.6 μg m−3 (mean: 5.75±4.24 μg m−3) during the measurement period. It was 9.29±4.11 μg m−3 during pre-LD (February 12–March 21), 4.70±0.95 μg m−3 during LD1 (March 25–April 14), 3.41±0.56 μg m−3 during LD2 (April 15–May 3), 3.69±1.50 μg m−3 during LD3 (May 4–17), 2.94±0.93 μg m−3 during LD4 (May 18–31), and 6.56±5.35 μg m−3 during the Post-LD (June 6–July 3) of 2020. It decreased up to 68% during the lockdowns. The source apportionment based on an improved method showed a significant improvement in the contribution of BC880 sources. The radiation effect determined by Angstrom Absorption Exponent showed that brown carbon accounted for 25% of the aerosol light absorption at 370 nm during the lockdown period. Relative humidity correlates substantially with BC880, while rainfall, temperature, and solar radiation were negatively correlated. The bivariate analysis showed the dominance of local emissions in the BC880 concentrations.Research highlightsBlack carbon concentration decreased up to 68% during the different phases of lockdown.BC associated with fossil fuel was 51–78%, and biomass burning was 22–49%.The fraction of fossil fuel and biomass burning in whole BC fallen to 0.73 and 0.65 during the lockdowns.Air quality improved by about 47–58% on the 4th and 7th day of lockdown.Brown carbon and meteorological parameters significantly impacted aerosol light absorption in this region.
ABSTRACT
Direct solar vapor generation (SVG) provides a sustainable and eco‐friendly solution to the current global water scarcity challenges. However, existing SVG systems operating under natural sunlight suffer from low water yield and high energy requirement of vaporization. New materials with reduced latent heat of water vaporization are in urgent demand to boost SVG process. Herein, we propose a novel strategy to additively fabricate anisotropic hybrid 3D structure from photocurable thermoresponsive p(NIPAm‐co‐PEGDA) hydrogel on the top of PEGDA foam for SVG. The in‐situ post‐printing synthesis of iron oxide nanoparticles within the p(NIPAm‐co‐PEGDA) hydrogel on the top surface, thus introducing anisotropy, is achieved by adding metallic salt precursor into the printing solution. The as‐fabricated hydrogel composite structure exhibits superior light absorption properties and rapid capillary‐driven water transport through a 3D‐printed microchannel network within the hydrogel. As a result, our SVG device achieves an extraordinary water evaporation rate of 5.12 kg m−2 h−1 under one sun (1 kW/m2). The intrinsic water activation states, in addition to wettability modulation with temperature increase within p(NIPAm‐co‐PEGDA) hydrogel, plays a critical role in reducing the equivalent vaporization enthalpy and shifting the vaporization to relatively lower temperatures. The proposed hybrid SVG device is feasible, portable, and highly efficient, promising great potential for grand water‐energy nexus challenges.