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The physical treatment of internal mixing and aging of black carbon (BC) aerosols that allow for enhanced solar absorption of the BC is an important parameterization in climate models. Many climate ...

Carbon nitride (g-C3N4) has attracted great attention for its wide applications in hydrogen evolution and photocatalytic degradation. In this study, phosphorus doped porous ultrathin carbon nitride nanosheets (PCN-S) were prepared successfully via the element doping and thermal exfoliation method. The prepared PCN-S was characterized by XRD, SEM, TEM, N2-adsorption-desorption measurement, FT-IR, XPS, UV–vis diffuse reflectance spectra, photoluminescence (PL), photocurrent response (I-t) and EIS. The results show that PCN-S owns regular crystal structure of g-C3N4, large specific surface areas and nanosheet structure with lots of in-plane pores on its surface, excellent chemical stability, and broad light response to the whole visible light region, which was attributed to the doping of phosphorus element. Under visible light irradiation, the photocatalytic reduction of Cr(VI) over different samples indicated that the P doping and porous nanosheet structure play an important role for the enhanced performance of PCN-S. The reason was that P element doping can broaden the visible light response region, and large specific surface areas from the porous nanosheet structure can provide quantities of active sites for the photocatalytic reaction. Then the detailed study on the PCN-S for simultaneous photocatalytic reduction of Cr(VI) and oxidation of 2,4-diclorophenol (2,4-DCP) was conducted. The experiments results show that low pH value and enough dissolved oxygen were found to promote Cr(VI) reduction and 2,4-DCP oxidation. The detailed photocatalytic mechanism was proposed. The strategies used in this study could provide new insight into the design of g-C3N4 based materials with high photocatalytic activity, and present potential for the treatment of Cr(VI)/2,4-DCP or other mixed pollutants in wastewater.

Black carbon (BC) is an important pollutant for both air quality and earth's radiation balance because of its strong absorption enhancement. The enhanced light absorption of BC caused by other pollutants is one of the most important sources of uncertainty in global radiative forcing. The light absorption of BC is highly dependent on the emission source and very few studies have been carried out for the source apportionment of BC absorption enhancement. Thus, with this objective, continuous measurements of particulate matter (PM2.5) were performed at three different sites: a traffic site in Nanjing, an urban site in Jinan, and a rural site in Yucheng; the BC absorption enhancement and its source contributions were determined. The mass absorption cross-section (MAC) of BC aerosols was reduced after the removal of the coating material. The maximum MAC enhancement (EMAC) was found to be 2.25 ± 0.5 at the rural site, followed by 2.07 ± 0.7 at the urban site and 1.7 ± 0.6 at the traffic site, suggesting an approximately double enhancement in BC absorption due to different coating materials. The source apportionment of absorption enhancement of BC analysis using the positive matrix factorization model suggests five major emission sources. Among them, secondary sources were the main source of EMAC at all the three sites with a percentage contribution of 43.4% (rural site), 34.6% (traffic site), and 31% (urban site). However, other emission sources, such as biomass burning (21.1% at rural site) and vehicular emissions (33.8% at traffic site) also had a significant contribution to EMAC, suggesting that there could be large variations in BC absorption enhancement due to differences in emission sources together with aerosol aging processes.