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Uptake of nitrous acid and nitrogen oxides by nylon surfaces: Implications for nitric acid measurement
Institution:1. Departamento de Agricultura y Alimentación, Universidad de La Rioja, Av. Madre de Dios 51, 26006 Logroño, Spain;2. Departamento de Ingeniería y Ciencias Agrarias, ESTI Agraria, Universidad de León, Av. Portugal 41, 24071 León, Spain;1. Department of Environmental Engineering, School of Resource and Environmental Science, Wuhan University, Hubei, Wuhan, 430079, China;2. State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China;3. Department of Atmospheric Science, School of Environmental Science and Engineering, Sun Yat-Sen University, Guangzhou 510275, China;4. Institute of Tropical and Marine Meteorology, China Meteorological Administration, Guangzhou 510080, China
Abstract:The interference in HNO3 determination due to HNO2 and NOx retention on nylon filters has been evaluated in laboratory and field conditions. Nitrous acid is retained on nylon filters with efficiencies varying from 25% at 12ℓ min−1 to 80% at 2ℓ min−1, yielding NO2 ion. In ambient sampling performed during photochemical smog episodes, NO2 is oxidized to NO3 with conversion factors up to 100%, resulting in a positive bias in HNO3 determination.NO2 reacts heterogeneously with H2O on nylon surfaces according to the reaction 2NO2 + H2O → HNO2 + HNO3 with a removal constant of about 1 × 10−4 ms−1 at a H2O concentration of 20,000 ppm. The resulting nitrite and nitrate are independent of the sampling flow rate, while NO2 concentration, sampling time and exposed nylon surface area play a directly proportional role. Accordingly, the relative interference of NO2 with respect to HNO3 determination is almost negligible for nylon filters, usually run at relatively high flow rates, while it may be significant for nylon denuders, which are characterized by larger exposed surfaces and lower operating flow rates.
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