Changes of air pollutants and simulation of a heavy pollution process during COVID-19 in Shenyang.

During COVID-19, Shenyang implemented strict household isolation measures, resulting in a sharp reduction in anthropogenic emission sources, providing an opportunity to explore the impact of human activities on air pollution. The period from January to April of 2020 was divided into normal period, blockade period and resumption period. Combined with meteorological and pollutant data, mathematical statistics and spatial analysis methods were used to compare with the same period of 2015-2019. The results showed that PM2.5, PM10, NO2 and O3 increased by 32.6%, 13.2%, 4.65% and 22.7% in the normal period, among which the western area changed significantly. During the blockade period, the concentration of pollutants decreased by 35.79%, 35.87%, 32.45% and -4.84%, of which the central area changed significantly. During the resumption period, the concentration of pollutants increased by 21.8%, 8.7%, 5.7% and -6.3%, and the area with the largest change was located in the western. During the blockade period, a heavy pollution occurred with PM2.5 as the main pollutant. The WRF-Chem model and the HYSPLIT model were used to reproduce the pollution occurrence process. The result showed that winds circulated as zonal winds during the pollution process at high altitudes. These winds were controlled by straight westerly and weak northwesterly airflows in front of the high pressure, and the ground was located behind the warm low pressure. Weather conditions were relatively stable. Thus, high temperatures (average > 10 ℃), high humidity (40%-60%) and slow wind (2 m/s) conditions prevailed for a long time in the Shenyang area. The unfavorable meteorological conditions lead to the occurrence of pollution. The backward trajectory showed that the potential source areas were concentrated in the urban agglomeration around Shenyang, and sporadic contributions came from North Korea.

Fabrication of S-scheme CdS-g-C3N4-graphene aerogel heterojunction for enhanced visible light driven photocatalysis.

Constructing S-scheme heterojunction photocatalysts reveals a greatly improved separation efficiency of photogenerated carriers and enhanced harvesting ability of solar energy in photocatalytic field. Herein, a ternary CdS-g-C3N4-GA heterojunction has been fabricated by a facile ultrasound strategy, which behaved as a S-scheme heterojunction with an intimate interface formed, and GA played as an electronic transportation platform to promote the separation of photo-induced charge carriers, which was certified through photoelectrochemical techniques. Density functional theory calculations revealed that the different component in ternary CdS-g-C3N4-GA heterojunction demonstrated an obvious difference of work function, resulting in the charge transfer from CdS to g-C3N4 through GA with S-scheme principle. In the optimized conditions, the S-scheme CdS-g-C3N4-GA heterojunction not only displayed greatly enhanced photocatalytic performances for degradation of dye and antibiotic wastewater, but also improved photocatalytic H2 production activity. In addition, the photocatalytic mechanism and driving force of charge transfer and separation in S-scheme CdS-g-C3N4-GA heterojunction were studied. This study offers a feasible strategy to construct a ternary S-scheme heterojunction for environmental and energy photocatalysis.