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Abstract: The kinetics of the heterogeneous reaction between gaseous HCHO and TiO2/SiO2 mineral coatings were investigated using a coated-wall flow tube to mimic HCHO loss on mineral aerosol and TiO2 coated depolluting urban surfaces. The measured uptake kinetics were strongly enhanced when the flow tube was irradiated with 340–420 nm UV light with an irradiance of 1.45 mW cm−2. The associated BET uptake coefficients ranged from (3.00 ± 0.45) × 10−9 to (2.26 ± 0.34) × 10−6 and were strongly dependent on HCHO initial concentration, relative humidity, temperature, and TiO2 content in the mineral coating, which ranged from 3.5 to 32.5 ppbv, 6–70%, 278–303 K, and 1–100 %wt, respectively. The measured kinetics were well described using a Langmuir–Hinshelwood type formalism. The estimated uptake coefficients were used to discuss the importance of heterogeneous HCHO surface loss, in terms of deposition lifetimes, as compared to major homogeneous gas-phase losses such as OH reaction and photolysis. It is found that deposition may compete with gas-phase removal of HCHO in a dense urban environment if more than 10% of the urban surface is covered with TiO2 treated material. [ABSTRACT FROM AUTHOR]

Abstract: Simultaneous measurements of aerosol absorption and scattering coefficients for the PM2.5 aerosols particles were done at Delhi during April 2008–March 2009 to estimate the aerosol single scattering albedo (SSA) and the Angstrom absorption exponents at the surface. The annual average SSA at 0.55 μm was found to be 0.70 ± 0.07 with only slight variations during the four seasons, summer (0.63 ± 0.06), monsoon (0.69 ± 0.07), winter (0.74 ± 0.03) and spring (0.72 ± 0.04). However, large variations in average absorption and scattering coefficients were seen during these four seasons. The average absorption coefficients during summer, monsoon, winter and spring were found to be 62.47 ± 21.27, 50.95 ± 43.61, 189.65 ± 85.94 and 90.65 ± 33.06 Mm−1 respectively. The corresponding scattering coefficients were 110.46 ± 36.15, 95.34 ± 49.46, 565.59 ± 274.59 and 236.56 ± 96.25 Mm−1. The Angstrom absorption exponent (ασ(abs)) remained close to unity throughout the year averaging at 1.02 ± 0.08, 1.02 ± 0.10, 1.04 ± 0.11, and 1.03 ± 0.05 during summer, monsoon, winter and spring seasons respectively, strongly indicating that the absorption at Delhi aerosol is mainly due to the abundance of black carbon of fossil fuel origin. [ABSTRACT FROM AUTHOR]

Abstract: Ultrafine particles (UFPs) released from laser printers are electrostatically charged during the working processes of the devices, and the electrostatic force can obviously influence the dynamics of the particles. Due to the measurement difficulty and scarcity of relevant research, this issue was not reported. This study tried to address this issue through experimental measurement of the surface charge of UFPs and numerical investigation on the influence of electrostatic force on the dynamics of UFPs. A test chamber was set up to collect the UFPs, and the Scanning Electron Microscope was used to observe the morphologies of the UFPs. Based on the particle diameter and surface zeta potential, the surface charge of UFPs was calculated. The measurement results gave that particle emitted from laser printers are negatively charged and the average surface charge of particle emissions for four laser printers is in a range of about −4.16 × 10−17 to −6.07 × 10−17 C (∼−260 to −379 e). This paper also discussed the influence of electrostatic force on the dynamics of UFPs. According to the numerical investigation, it was found that, in the absence of electric field, the electrostatic force has to be considered when the surface charge is larger than 1 × 10−16 C and when the UFP is very close to the wall with a distance of less than 0.01 m. These findings will guide constructively in predicting the dispersion and deposition of particles emitted from laser printers. [Copyright &y& Elsevier]

Abstract: Organic films, collected from indoor and outdoor window surfaces in Guangzhou and Hong Kong of South China, were analyzed to quantify their organic carbon (OC), elemental carbon (EC), and polybrominated diphenyl ethers (PBDEs) content. The highest concentrations of OC, EC, and BDE-209 were found in Guangzhou with values of 10 000 μg m−2, 2200 μg m−2, and 4000 ng m−2, respectively, and the highest concentration of Σ7PBDE (sum of BDE-28, -47, -99, -100, -153, -154 and -183) was found in Hong Kong with a value of 25 ng m−2. In most cases, the concentrations of PBDEs were higher in the exterior films than those in the interior films with BDE-209 as the predominant congener in both cities, suggesting that PBDEs mainly come from ambient environment, and deca-BDE accounts for major PBDE consumption. The growth rates of organic film on window surfaces were fast at the beginning, and reached a consistent level afterwards. The evolution rates ranged from 2.6 to 11 nm day−1 for “bulk film”, while from 0.06 to 0.92 nm day−1 for “pure film”. The concentrations of PBDEs on the window surfaces did not increase with the growth time, suggesting that the window surface may provide a good place for photo-degradation of PBDEs. [Copyright &y& Elsevier]