Enhancing the removal of Sb (III) from water:a Fe3O4@HCO composite adsorbent caged in sodium alginate microbeads

To remove antimony (Sb) ions from water, a novel composite adsorbent was fabricated from ferriferous oxide and waste sludge from a chemical polishing process (Fe3O4@HCO) and encapsulated in sodium alginate (SAB). The SAB adsorbent performed well with 80%–96% removal of Sb (III) ions within a concentration range of 5–60 mg/L. The adsorption mechanism of Sb (III) was revealed to be the synergy of chemisorption (ion exchange) and physisorption (diffusion reaction). The adsorption isotherms and kinetics conformed to the Langmuir isotherm and the pesudo-second-order kinetic model. Both initial pH and temperature influenced the adsorption performance with no collapse of microbeads within solution pH range 3–7. Most importantly for practical applications, these microspheres can be separated and recovered from aqueous solution by a magnetic separation technology to facilitate large-scale treatment of antimony-containing wastewater

Study on the migration rules of Sb in antimony ore soil based on HYDRUS-1D

https://egrove.olemiss.edu/aicpa_comm/1198/thumbnail.jp

Ambient volatile organic compounds in a suburban site between Beijing and Tianjin : Concentration levels, source apportionment and health risk assessment

Volatile organic compounds (VOCs) have vital implications for secondary pollutants, atmospheric oxidation and human health. Ambient VOCs were investigated using an online system, gas chromatography-mass spectrometry/flame ionization detector (GC-MS/FID), at a suburban site in Xianghe in the North China Plain from 6 November 2017 to 29 January 2018. Positive matrix factorization (PMF) receptor model was applied to identify the major VOC contributing sources. Four-step health risk assessment method was used to estimate risks of all risk-posing VOC species. A total of 101 VOCs were quantified, and the mean concentration of total VOCs was 61.04 +/- 65.18 ppbv. The VOCs were dominated by alkanes (38.76%), followed by alkenes, aromatics, halocarbons, OVOCs, acetylene and acetonitrile. The results of PMF revealed that vehicle exhaust, industrial emissions, liquefied petroleum gas & natural gas, solvent utilization and secondary and long-lived species contributed 31.0%, 26.4%, 18.6%, 13.6% and 10.4%, respectively, to the total VOCs. Pollutant-specific and source-specific non-carcinogenic and carcinogenic risk estimates were conducted, which showed that acrolein and vehicle exhaust had evident noncarcinogenic risks of 4.9 and 0.9, respectively. The carcinogenic risks of specific species (1,3-butadiene, acetaldehyde, benzene, chloroformand 1,2-dichloroethane) and identified sources were above the United States Environmental Protection Agency (USEPA) acceptable level (1.0 x 10(-6)) but below the tolerable risk level (1.0 x 10(-4)). Vehicle exhaust was the largest contributor (56.2%) to noncarcinogenic risk, but solvent utilization (32.6%) to carcinogenic risk. Moreover, with the evolution of pollution levels, almost all VOC species, contributions of alkenes, aromatics, solvent utilization and vehicle exhaust, and pollutant-specific and source-specific risks increased continuously and noticeably. Collectively, our findings unraveled the importance of alkenes, aromatics, solvent utilization and vehicle exhaust in the evolution of pollution levels. Future studies should consider targeting these VOC groups and sources when focusing on effective reduction strategies and assessing public health risks. (c) 2019 Elsevier B.V. All rights reserved.Peer reviewe

Impact of primary and secondary air supply intensity in stove on emissions of size-segregated particulate matter and carbonaceous aerosols from apple tree wood burning

In order to assess emission factors (EF) more accurately from household biomass burning, a series of laboratory controlled apple tree wood burning tests were conducted to measure the EFs of size-segregated particulate matter (PM) and carbonaceous aerosols. The controlled burning experiments were conducted with designed primary air (PA) and secondary air (SA) supply intensity. An optimum value of 7 m(3).h(-1) was found for SA, resulting the highest modified combustion efficiency (92.4 +/- 2.5%) as well as the lowest EFs of PM2.5 (0.13 +/- 0.01 g.MJ(-1)), OC (0.04 +/- 0.03 g.MJ(-1)) and EC (0.03 +/- 0.01 g.MJ(-1)). SA values of 7 and 10 m(3).h(-1) resulted the lowest EFs for all the different PM sizes. In a test with PA of 6 m(3.)h(-1) and SA of 7 m(3).h(-1), very low EFs were observed for 0C1 (8.2%), 0C2 (11.2%) and especially OP (Pyrolyzed OC) (0%, not detected), indicating nearly complete combustion under this air supply condition. Besides SA, higher PA was proved to have positive effects on PM and carbonaceous fraction emission reduction. For example, with a fixed SA of 1.5 m(3).h(-1), EFs of PM2.5 decreased from 0.64 to 0.27 g.MJ(-1) when PA increased from 6 to 15 m(3).h(-1) (P < 0.05). Similar reductions were also observed in EFs of OC, EC and size segregated PM

Exploring the inorganic and organic nitrate aerosol formation regimes at a suburban site on the North China Plain

Nitrate-driven aerosol pollution frequently occurs during winter over the North China Plain (NCP). Extensive studies have focused on inorganic nitrate formation, but few have focused on organic nitrates in China, preduding a thorough understanding of the nitrogen cycle and nitrate aerosol formation. Here, the inorganic (NO3,inorg) and organic nitrate (NO3,org) formation regimes under aerosol liquid water (ALW) and aerosol acidity (pH) influences were investigated during winter over the NCP based on data derived from an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS). The campaign-averaged concentration of the total nitrate was 53 mu g m(3), with a 13% contribution from NO3,org, which exhibited a significantly decreased contribution with increasing haze episode evolution. The diurnal cycles of NO3,inorg and NO3,org were similar, with high concentrations during the nighttime at a high ALW level, revealing the important role of aqueous-phase processes. However, the correlations between the aerosol pH and NO3,inorg (R-2 = 0.13, P <0.01) and NO3,org (R-2 = 0.63, P <0.01) during polluted periods indicated a contrasting effect of aerosol pH on inorganic and organic nitrate formation. Our results provide a useful reference for smog chamber studies and promote a better understanding of organic nitrate formation via a nthropogenic emissions. (C) 2021 Elsevier B.V. All rights reserved.Peer reviewe