Simultaneous removal of nitrogen oxides and sulfur dioxide using ultrasonically atomized hydrogen peroxide

A new method was developed for denitrification and desulfurization using hydrogen peroxide with the aid of an ultrasonic nebulizer to obtain high removal efficiency of NOx and SO 2 . Comparing with the atomizing nozzles having the aperture size of 0.01~0.02 mm, the droplets generated using the ultra...

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Veröffentlicht in:Environmental science and pollution research international 2019-08, Vol.26 (22), p.22351-22361
Hauptverfasser: Wei, Jiaqi, Gu, Junjie, Guo, Junheng, Li, Wei, Wang, Chenglong, Zhang, Jinli
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container_issue 22
container_start_page 22351
container_title Environmental science and pollution research international
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creator Wei, Jiaqi
Gu, Junjie
Guo, Junheng
Li, Wei
Wang, Chenglong
Zhang, Jinli
description A new method was developed for denitrification and desulfurization using hydrogen peroxide with the aid of an ultrasonic nebulizer to obtain high removal efficiency of NOx and SO 2 . Comparing with the atomizing nozzles having the aperture size of 0.01~0.02 mm, the droplets generated using the ultrasonic nebulizer show the smallest d 50 value of 7.2 μm, with 72% possessing the size less than 10 μm. Based on the numerical simulation of the vaporization rate of droplets, it is indicated that the droplets with the size of 7.2 μm can be vaporized totally at very short residence time (0.11 s) under 130 °C. Effects of influence factors including the reaction temperature, the initial H 2 O 2 concentration, pH value, and the flue gas flow rate were studied on the removal efficiencies of NO and SO 2 . Using the in-series double-oxidation subsystems with H 2 O 2 concentration of 6 wt%, pH 5.0, and the reaction temperature of 130 °C, the removal efficiencies of SO 2 and NO are respectively 100% and 89.3% at the short residence time of 1.8 s, and the removal efficiency of NO can be increased to 100% as the residence time is longer than 3.7 s. It is confirmed that the ultrasonically atomized H 2 O 2 can indeed enhance the removal efficiencies of NO and SO 2 at the optimal temperature, owing to the fast vaporization rate of fine droplets as well as the formation of more active radicals to be captured by NO and SO 2 simultaneously. The results here provide a promising route to remove effectively the emissions of NO and SO 2 simultaneously. Graphical abstract
doi_str_mv 10.1007/s11356-019-05531-1
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Comparing with the atomizing nozzles having the aperture size of 0.01~0.02 mm, the droplets generated using the ultrasonic nebulizer show the smallest d 50 value of 7.2 μm, with 72% possessing the size less than 10 μm. Based on the numerical simulation of the vaporization rate of droplets, it is indicated that the droplets with the size of 7.2 μm can be vaporized totally at very short residence time (0.11 s) under 130 °C. Effects of influence factors including the reaction temperature, the initial H 2 O 2 concentration, pH value, and the flue gas flow rate were studied on the removal efficiencies of NO and SO 2 . Using the in-series double-oxidation subsystems with H 2 O 2 concentration of 6 wt%, pH 5.0, and the reaction temperature of 130 °C, the removal efficiencies of SO 2 and NO are respectively 100% and 89.3% at the short residence time of 1.8 s, and the removal efficiency of NO can be increased to 100% as the residence time is longer than 3.7 s. 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Comparing with the atomizing nozzles having the aperture size of 0.01~0.02 mm, the droplets generated using the ultrasonic nebulizer show the smallest d 50 value of 7.2 μm, with 72% possessing the size less than 10 μm. Based on the numerical simulation of the vaporization rate of droplets, it is indicated that the droplets with the size of 7.2 μm can be vaporized totally at very short residence time (0.11 s) under 130 °C. Effects of influence factors including the reaction temperature, the initial H 2 O 2 concentration, pH value, and the flue gas flow rate were studied on the removal efficiencies of NO and SO 2 . Using the in-series double-oxidation subsystems with H 2 O 2 concentration of 6 wt%, pH 5.0, and the reaction temperature of 130 °C, the removal efficiencies of SO 2 and NO are respectively 100% and 89.3% at the short residence time of 1.8 s, and the removal efficiency of NO can be increased to 100% as the residence time is longer than 3.7 s. It is confirmed that the ultrasonically atomized H 2 O 2 can indeed enhance the removal efficiencies of NO and SO 2 at the optimal temperature, owing to the fast vaporization rate of fine droplets as well as the formation of more active radicals to be captured by NO and SO 2 simultaneously. The results here provide a promising route to remove effectively the emissions of NO and SO 2 simultaneously. 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Comparing with the atomizing nozzles having the aperture size of 0.01~0.02 mm, the droplets generated using the ultrasonic nebulizer show the smallest d 50 value of 7.2 μm, with 72% possessing the size less than 10 μm. Based on the numerical simulation of the vaporization rate of droplets, it is indicated that the droplets with the size of 7.2 μm can be vaporized totally at very short residence time (0.11 s) under 130 °C. Effects of influence factors including the reaction temperature, the initial H 2 O 2 concentration, pH value, and the flue gas flow rate were studied on the removal efficiencies of NO and SO 2 . Using the in-series double-oxidation subsystems with H 2 O 2 concentration of 6 wt%, pH 5.0, and the reaction temperature of 130 °C, the removal efficiencies of SO 2 and NO are respectively 100% and 89.3% at the short residence time of 1.8 s, and the removal efficiency of NO can be increased to 100% as the residence time is longer than 3.7 s. It is confirmed that the ultrasonically atomized H 2 O 2 can indeed enhance the removal efficiencies of NO and SO 2 at the optimal temperature, owing to the fast vaporization rate of fine droplets as well as the formation of more active radicals to be captured by NO and SO 2 simultaneously. The results here provide a promising route to remove effectively the emissions of NO and SO 2 simultaneously. Graphical abstract</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>31154651</pmid><doi>10.1007/s11356-019-05531-1</doi><tpages>11</tpages></addata></record>
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source SpringerNature Journals
subjects Apertures
Aquatic Pollution
Atmospheric Protection/Air Quality Control/Air Pollution
Atomizing
Chemical engineering
Compressed air
Computer simulation
Denitrification
Droplets
Earth and Environmental Science
Ecotoxicology
Efficiency
Environment
Environmental Chemistry
Environmental Health
Environmental science
Flow rates
Flow velocity
Flue gas
Gas flow
Hydrogen peroxide
Mathematical models
Nitrogen
Nitrogen oxides
Nitrogen removal
Nozzles
Oxidation
Oxides
pH effects
Photochemicals
Research Article
Residence time distribution
Simulation
Subsystems
Sulfur
Sulfur dioxide
Temperature effects
Vaporization
Waste Water Technology
Water Management
Water Pollution Control
title Simultaneous removal of nitrogen oxides and sulfur dioxide using ultrasonically atomized hydrogen peroxide
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