Hydroxyl Radical Concentration in Ambient Air at a Semirural Site Estimated from C13O Oxidation

Author(s):  
J. Hjorth ◽  
G. Ottobrini ◽  
F. Cappellani ◽  
G. Restelli ◽  
H. Stangl ◽  
...  
1985 ◽  
pp. 725-729 ◽  
Author(s):  
J. Hjorth ◽  
G. Ottobrini ◽  
F. Cappellani ◽  
G. Restelli ◽  
H. Stangl ◽  
...  

Talanta ◽  
2020 ◽  
Vol 218 ◽  
pp. 121148 ◽  
Author(s):  
Ronald S. Lankone ◽  
Alyssa R. Deline ◽  
Michael Barclay ◽  
D. Howard Fairbrother

1980 ◽  
Vol 14 (1) ◽  
pp. 93-97 ◽  
Author(s):  
Hajime. Akimoto ◽  
Fumio. Sakamaki ◽  
Gen. Inoue ◽  
Michio. Okuda

Science ◽  
1975 ◽  
Vol 189 (4205) ◽  
pp. 797-800 ◽  
Author(s):  
C. C. Wang ◽  
L. I. Davis ◽  
C. H. Wu ◽  
S. Japar ◽  
H. Niki ◽  
...  
Keyword(s):  

2020 ◽  
Author(s):  
Fengyang Wang ◽  
Renzhi Hu ◽  
Pinhua Xie ◽  
Yihui Wang ◽  
Shengrong Lou ◽  
...  

<p>Hydroxyl (OH) play an essential role in atmospheric chemistry. OH radical is an indicator of atmospheric oxidation and self-purification, which determines the removal of most trace gases in the atmosphere, such as CO, SO<sub>2</sub>, NO<sub>2</sub>, CH<sub>4</sub> and other volatile organic compounds (VOCs). A ground-based system for measurement of tropospheric OH radical by Laser Induced Fluorescence technique (AIOFM-LIF) was developed and integrated into a mobile observation platform for field observation. Ambient air expands through a 0.4 mm nozzle to low pressure. OH radical is irradiated by the 308 nm laser pulse at a repetition rate of 8.5 kHz, accompanying the release fluorescence of the A<sup>2</sup>Σ<sup>+</sup>(v’=0)—X<sup>2</sup>Π<sub>i</sub>(v’’=0) transition at 308 nm with the resultant fluorescence being detected by gated photon counting. The detection sensitivity of AIOFM-LIF system was calibrated by a portable standard OH radical source based on water photolysis-ozone actinometry. Following laboratory and field calibrations to characterise the instrument sensitivity, OH radical detection limits were (1.84±0.26) × 10<sup>5</sup> cm<sup>-3</sup> and (3.69±0.52) × 10<sup>5</sup> cm<sup>-3</sup> at night and noon, respectively. During “A comprehensive STudy of the Ozone foRmation Mechanism in Shenzhen” (STORM) campaign, AIOFM-LIF system was deployed in Shenzhen, China, and OH radical concentration was obtained validly except for the rainy days. Mean diurnal variation of HOx radical concentration was obtained, and the peak was 6.6×10<sup>6</sup> cm<sup>-3</sup> which appeared around 12:00 at noon. A general good agreement of OH radical concentration with j(O<sup>1</sup>D) was observed with a high correlation (R<sup>2</sup> =0.77), which illustrates that photolysis of ozone is an important source of OH radical during this campaign. A box model was applied to simulate the concentrations of OH at this field site, the primary production of OH radical was generally dominated by photolysis of O<sub>3</sub>, HONO, HCHO, while the other production was contributed by calculated species (OVOCs).</p>


2020 ◽  
Vol 31 (1) ◽  
Author(s):  
Thuan Dao Nguyen

Recently, nonthermal atmospheric pressure plasma has been developed as a novel tool in removal of water pollutants. Rhodamine B dye, widely used in textiles and biology, is toxic to both humans and animals, hence removing residual Rhodamine B in solution is necessary. In this work, we have setup a cold plasma jet system and used it to effectively remove Rhodamine B in the solution. We have shown that the main oxidation substance responsible to remove Rhodamine B is the hydroxyl radical (•OH). By studying the effect of the hydrogen peroxide (H2O2) concentration in the initial and later was produced in the solution, the plasma power, and the Ar gas flow speed on the dye remove rate, we have identified 2 main reaction pathways to generate hydroxyl radical (•OH). Both of these reaction pathways involve high-energy electrons interacting with water and O2 in the solution and in the ambient air. Our work provides important information to understand the mechanism of dye removal by cold plasma treatment.


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