Heterogeneous aqueous reaction plays important roles in the enhanced formation of secondary aerosols during haze. However, its occurrence in haze episodes remains poorly understood. In this study, the trends in heterogeneous aqueous reaction in continuous haze episodes were investigated by an in-depth case analysis. The highly time-resolved measurements of water-soluble inorganic ions of PM were conducted in a suburban of Shanghai, China, and continuous haze episodes, which occurred from Feb. 18 to Feb. 28, were selected as studied cases. Results showed that fine particle pollution in Baoshan was serious. High concentrations of secondary inorganic aerosol ions and the higher sulfur oxidation ratio (SOR) and nitrogen oxidation ratio (NOR) on haze days indicated enhanced conversions from SO and NO to their corresponding particulate phases. The high-nitrate haze episode and the high-sulfate haze episode were identified. Further simulations revealed that the PM particles had strong acidity during the high-nitrate and high-sulfate haze episodes whether they were calculated by E-AIM 4 or by ISORROPIA II. It was found that particulate liquid water was more sensitive to nitrate than sulfate, and played significant roles in the heterogeneous aqueous reactions of NO and secondary nitrate formation during haze episodes, especially in the high-sulfate haze episode. Further analysis indicated that the high-nitrate haze episode favoured the occurrence of heterogeneous aqueous phase oxidation of SO, and the more water was in the particles, the more SO was converted to sulfate aerosols. This work provides an important field measurement-based evidence for understanding the important contributions of the heterogeneous aqueous reactions to secondary aerosol pollution and the tendencies of heterogeneous aqueous reactions in the formation of secondary sulfate and nitrate aerosols in suburban Shanghai.
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http://dx.doi.org/10.1016/j.scitotenv.2018.04.086 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
School of Chemistry and Chemical Engineering, State Key Laboratory of Metal Matrix Composites, Frontiers Science Center for Transformative Molecules, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China.
Hydrogel-based sensors typically demonstrate conspicuous swelling behavior in aqueous environments, which can severely compromise the mechanical integrity and distort sensing signals, thereby considerably constraining their widespread applicability. Drawing inspiration from the multilevel heterogeneous structures in biological tissues, an antiswelling hydrogel sensor endowed with high strength, rapid self-recovery, and low swelling ratio was fabricated through a water-induced phase separation and coordination cross-linking strategy. A dense heterogeneous architecture was developed by the integration of "rigid" quadridentate carboxyl-Zr coordination bonds and "soft" hydrophobic unit-rich regions featuring π-π stacking and cation-π interactions into the hydrogels.
View Article and Find Full Text PDFInnovation (Camb)
January 2025
International Joint Laboratory of Catalytic Chemistry, College of Sciences, Shanghai University, Shanghai 200444, China.
Heterogeneous catalysis at the metal surface generally involves the transport of molecules through the interfacial water layer to access the surface, which is a rate-determining step at the nanoscale. In this study, taking the oxygen reduction reaction on a metal electrode in aqueous solution as an example, using accurate molecular dynamic simulations, we propose a novel long-range regulation strategy in which midinfrared stimulation (MIRS) with a frequency of approximately 1,000 cm is applied to nonthermally induce the structural transition of interfacial water from an ordered to disordered state, facilitating the access of oxygen molecules to metal surfaces at room temperature and increasing the oxygen reduction activity 50-fold. Impressively, the theoretical prediction is confirmed by the experimental observation of a significant discharge voltage increase in zinc-air batteries under MIRS.
View Article and Find Full Text PDFSci Rep
January 2025
Department of Chemistry, Faculty of Science, Arak University, Arak, 38481-77584, Iran.
In this study, a novel hybrid nanostructure consisting of acid-decorated chitosan and magnetic AlFeO nanoparticles was fabricated. The acid-decorated chitosan provided a stable and biocompatible matrix for the magnetic AlFeO nanoparticles. Various techniques including Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction patterns (XRD), thermogravimetric analysis (TGA), vibrating sample magnetometry (VSM), specific surface area (BET), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS) were used to characterize and confirm the successful synthesis of the hybrid nanostructure.
View Article and Find Full Text PDFJ Phys Chem B
January 2025
Department of Chemistry, Birla Institute of Technology and Science, Pilani, Pilani Campus, Rajasthan 333031, India.
The behavior of water in concentrated ionic solutions, including supersaturated conditions, is crucial for numerous material and energy conversion processes and fundamental research. All electrolytes whether they "structure-make" or "structure-break" the water structure lead to slower water motion. This study investigates the structure and dynamics of aqueous NaCl solutions across a wide range of concentrations.
View Article and Find Full Text PDFJ Environ Manage
January 2025
School of Environmental Science and Engineering, Changzhou University, Changzhou, 213164, PR China.
Compared with zero-valent iron, iron sulfide has more diverse reactive species and higher reductivity, but it is still prone to be gradually deactivated due to various passivation factors. In this study, a novel reductive material (BMMW@OA) was prepared by ball milling of mackinawite (MW) as raw material and oxalic acid (OA) as modifier, so as to simultaneously improve its reductivity and stability by continuous releasing reductive species and maintaining freshness of the material surface. The BMMW@OA (w/w of MW/OA = 4/1) effectively removed Cr(Ⅵ) from water with wide pH adaptability.
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