Hydroxyl Radical Reactivity with Nitrobenzene in Subcritical and Supercritical Water

2002 ◽  
Vol 124 (22) ◽  
pp. 6304-6311 ◽  
Author(s):  
Junbo Feng ◽  
Sudhir N. V. K. Aki ◽  
John E. Chateauneuf ◽  
Joan F. Brennecke
Science ◽  
1977 ◽  
Vol 197 (4311) ◽  
pp. 1365-1367 ◽  
Author(s):  
R. A. GORSE ◽  
R. R. LII ◽  
B. B. SAUNDERS

2020 ◽  
Vol 740 ◽  
pp. 139897
Author(s):  
Jiaru Li ◽  
Yosuke Sakamoto ◽  
Nanase Kohno ◽  
Tomihide Fujii ◽  
Kohei Matsuoka ◽  
...  

2010 ◽  
Vol 132 (9) ◽  
pp. 2907-2913 ◽  
Author(s):  
Susan Mitroka ◽  
Stephanie Zimmeck ◽  
Diego Troya ◽  
James M. Tanko

Author(s):  
Donald T. Sawyer ◽  
R. J. P. Williams

Oxygen radicals are defined as those molecules that contain an oxygen atom with an unpaired, nonbonding electron (e.g., HO·). Although triplet dioxygen (·O2·) and superoxide ion (O2 - ·) come under this definition, their nonradical chemistry dominates their reactivity, which is discussed in Chapters 6 (·O2·) and 7 (O2-·). The hydroxyl radical (HO·) is the most reactive member of the family of oxygen radicals [HO·, RO·, ·O·, HOO·, ROO·, and RC(O)O·], and is the focus of most oxygen radical research. In the gas phase the dramatic example of oxygen radical reactivity with hydrocarbon substrates is combustion, which is initiated by HO· (or RO· or MO·) and propagated by ·O2· and ·O·.


2014 ◽  
Vol 14 (6) ◽  
pp. 2923-2937 ◽  
Author(s):  
R. F. Hansen ◽  
S. M. Griffith ◽  
S. Dusanter ◽  
P. S. Rickly ◽  
P. S. Stevens ◽  
...  

Abstract. Total hydroxyl radical (OH) reactivity was measured at the PROPHET (Program for Research on Oxidants: PHotochemistry, Emissions, and Transport) forested field site in northern Michigan during the 2009 Community Atmosphere–Biosphere INteraction EXperiment (CABINEX). OH reactivity measurements were made with a turbulent-flow reactor instrument at three heights from the forest floor above (21 and 31 m) and below (6 m) the canopy at three different time periods during the CABINEX campaign. In addition to total OH reactivity measurements, collocated measurements of volatile organic compounds (VOCs), inorganic species, and ambient temperature were made at the different heights. These ancillary measurements were used to calculate the total OH reactivity, which was then compared to the measured values. Discrepancies between the measured and calculated OH reactivity, on the order of 1–24 s−1, were observed during the daytime above the canopy at the 21 and 31 m heights, as previously reported for this site. The measured OH reactivity below the canopy during the daytime was generally lower than that observed above the canopy. Closer analysis of the measurements of OH reactivity and trace gases suggests that the missing OH reactivity could come from oxidation products of VOCs. These results suggest that additional unmeasured trace gases, likely oxidation products, are needed to fully account for the OH reactivity measured during CABINEX.


2003 ◽  
Vol 107 (50) ◽  
pp. 11043-11048 ◽  
Author(s):  
Junbo Feng ◽  
Sudhir N. V. K. Aki ◽  
John E. Chateauneuf ◽  
Joan F. Brennecke

2013 ◽  
Vol 40 (3) ◽  
pp. 973-990 ◽  
Author(s):  
Jiaming Zhang ◽  
Chunyuan Ma ◽  
Youmin Sun ◽  
Xiaohua Ren

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