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Mesoporous graphenes (MPGs) with interpenetrating porous networks are successfully obtained by the pyrolysis of composite gel consisting of graphite oxide (GO) and the amphiphilic triblock copolymer (Pluronic P123) under Ar atmosphere, wherein P123 is used as a soft-template. The as-prepared composite gel is obtained following self-assembly and freeze-drying. The obtained MPGs have high BET specific surface area (531-746 m2 g-1 and ink-bottle like pores with three dimensional interconnected network. Furthermore, the specific surface area and porous parameters such as pore volume, pore size, and pore size distribution of MPGs can be rationally controlled by regulating the initial mass ratio of P123 to GO. With the increase of P123 ratio, the average mesopore size is decreased from ∼16.4 nm to ∼9.5 nm, which is similar to the diameter size of P123 micelles. Also, the adsorption capacities of MPG-20 for 52 indoor air standard components (100 μg mL-1, Supelco) are compared with two different materials, namely commercial porous polymers (2,6-diphenyleneoxide) and reduced graphene oxide (RGO). The result shows that MPG-20 has significantly better adsorption capacity than RGO but also similar or slightly better than commercial porous polymer. The mesoporous structure and surface chemistry of MPGs were the most important factors for the enhancement of the adsorption efficiency for volatile organic compounds.

The synthesis and characterization of polymer-stabilized silver nanoparticles (Ag NPs) for water-based silver inks are studied. In order to synthesize Ag NPs with spherical shape, the conventional polyol processes require an excess of poly(vinyl pyrrolidone) (PVP) (10 ~ 1000 times than AgNO3) and therefore result in low productivity per reactor volume. In this study, poly(acrylic acid) (PAA) with carboxylic acid group was used instead of PVP. Even at less molar ratio of PAA to AgNO3 (< 2), the spherical Ag NPs with average size of 30 nm were successfully synthesized at 100 gram-scale with high reaction yield of 90%. Furthermore, the Ag NPs were dispersed into alcohol-based solvent and then patterned into metallic lines through inkjet printing technology.

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We measured PM2.5 in 41 underground shopping districts (USDs) in the Seoul metropolitan area from June to November 2017, and associated 18 trace elements to determine the sources and assess the respiratory risks. The PM2.5 concentrations were 18.0 ± 8.0 μg/m3 inside USDs, which were lower than 25.2 ± 10.6 μg/m3 outside. We identified five sources such as indoor miscellanea, soil dust, vehicle exhaust/cooking, coal combustion, and road/subway dust, using factor analysis. Almost 67% of the total trace element concentration resulted from soil dust. Soil dust contribution increased with the number of stores because of fugitive dust emissions due to an increase in passers-by. Vehicle exhaust/cooking contribution was higher when the entrances of the USDs were closed, whereas coal combustion contribution was higher when the entrances of the USDs were open. Although miscellanea and coal combustion contributions were 3.4% and 0.7%, respectively, among five elements with cancer risk, Cr and Ni were included in miscellanea, and Pb, Cd, and As were included in coal combustion. The excess cancer risk (ECR) was the highest at 67 × 10−6 for Cr, and the ECR for Pb was lower than 10−6, a goal of the United States Environmental Protection Agency for hazardous air pollutants.

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