As a carcinogenic pollutant, hexavalent chromium (Cr(VI)) in the ambient air has serious influences on public health. Due to its instability and difficulty in chemical analysis, few studies have been conducted on the regional concentration level of environmental Cr(VI), especially in China. The pollution levels of Cr(VI) in ambient PM_2.5 were determined in two sampling sites of Beijing and Qingdao from September to December 2020. The concentrations of Cr(VI) were determined using Ion Chromatography-inductively coupled plasma mass spectrometry(IC-ICP-MS), and the Cr concentrations were simultaneously analyzed by Inductively Coupled Plasma-atomic emission spectrometry(ICP-AES). The main results are as follows: (1) Based on the analysis of samples collected at the sampling sites of Beijing and Qingdao, the concentrations of Cr(VI) in PM_2.5 were (0.140 ± 0.065) ng/m³ and (0.091 ± 0.073) ng/m³, respectively; (2) During the sampling period, the mean ratio of Cr(VI) to Cr was (0.0623 ± 0.0969). The ratio of Cr(VI)/Cr in Beijing and Qingdao were 0.076 ± 0.104 and 0.041 ± 0.039, respectively. In conclusion, compared with other countries, the concentration of Cr(VI) at the sampling sites of Beijing and Qingdao showed lower values. The average concentration of Cr(VI) estimated by the ratio of this research in China is lower than that in South Korea and similar to those in Canada and Australia.

Pollutants emission, meteorological conditions, secondary formation, and pollutants transport are the main reasons for air pollution. A comprehensive air pollution analysis was conducted from the above four aspects in the autumn–winter seasons of 2017–2018 and 2018–2019 at Xingtai, China. In addition, the relationship between PM_2.5 and O₃ was also studied from the aspects of secondary formation and meteorological conditions to find the rules of cooperative management of PM_2.5 and O₃ combined pollution. Taking measures of concentrated and clean heating and controlling biomass burning could make the concentrations of EC, K⁺ and SO₄²⁻ decrease. The variation trends of PM_2.5 and O₃ concentration in the autumn–winter season of Xingtai were different, and with the increase in secondary formation effects, the concentration of O₃ decreased. Furthermore, the key meteorological conditions that affected O₃ and PM_2.5 formation were temperature and relative humidity, respectively. The relationships of NOR (nitrate oxidation rate) and SOR (sulfate oxidation rate) against temperature presented a “U” shape, suggesting that gas-phase oxidation and gas–solid-phase oxidation were all suppressed at a temperature of around 4 °C. The cities located in the east had more pollutant transporting effects during the pollution processes of Xingtai, and the main transport routes of O₃ and PM_2.5 were not all the same.

Non-methane hydrocarbons (NMHCs) from four sampling sites in Lanzhou, a petrochemical industrialized city in northwest China, was sampled by stainless steel canisters and measured by gas chromatography–mass selective detection/flame ionization detection (GC–MSD/FID) in May and June of 2017. Based on these results, the contributions of NMHCs to the ozone (O₃) and secondary organic aerosols (SOA), differences in tracer ratios, and source apportionment by principal component analysis (PCA) were analyzed. The results showed that the total NMHCs concentration in Lanzhou was 48.4 ± 48.3 ppbv (parts per billion by volume) during the observation and it was higher in May (78.6 ppbv) than in June (37.8 ppbv); the highest NMHCs concentration was observed in industrial areas. Alkanes were the dominant group at all sites in Lanzhou and account for more than 60% of the NMHCs, while isopentane, n-butane n-pentane, propane and ethane were the major compounds. Additionally, the NMHCs in Lanzhou have made great contributions to O₃ and SOA generation and the S1 site of the industrial area contributed the most to both of them. Propene, toluene, ethylbenzene and n-pentane were found to be more reactive with relatively high contributions to ozone formation. Aromatics and high carbon alkanes were major contributors to SOA formation potential (SOAp) (i.e., toluene, m,p-xylene, dodecane, undecane, n-tanane, benzene and ethylbenzene) in Lanzhou. Based on the specific volatile organic compounds (VOCs) ratio method and the PCA modem, the observation sites in Lanzhou were greatly affected by the surrounding industrial areas. The sources consisted of petrochemical industry, vehicle emissions, solvent usage and combustion sources, which contributed to 33.9%, 31.6%, 19.2% and 7.9% of the total monitored NMHCs, respectively. From different sites, though the influence of regional transport was not very significant on the whole, it also affected the NMHCs of nonindustrial areas based on the ratio of xylene to ethyl-benzene (X/E), especially the S4 site; vehicle emission was less important compared to sources from petrochemical industries in S1, as characterized by relatively higher toluene to benzene (T/B) ratios. However, vehicle emission has significant influence on NMHCs in S4. Overall, local emissions are the main source of NMHCs in Lanzhou and the petrochemical industry has a great influence on the distribution of NMHCs in the whole region.