Study on the Chemical Inhibition Mechanism of DBHA on Free Radical Reaction during Spontaneous Combustion of Coal

2020 ◽  
Vol 34 (5) ◽  
pp. 6355-6366
Author(s):  
Jie Wang ◽  
Yulong Zhang ◽  
Junfeng Wang ◽  
Chunshan Zhou ◽  
Yuguo Wu ◽  
...  
2017 ◽  
Vol 50 (2) ◽  
pp. 112-121 ◽  
Author(s):  
Dayanne L. H. Maia ◽  
Elenilson G. Alves Filho ◽  
Antonino F. Barros Junior ◽  
Fabiano A. N. Fernandes

Fuel ◽  
2022 ◽  
Vol 310 ◽  
pp. 122240
Author(s):  
Zhian Huang ◽  
Sainan Quan ◽  
Xiangming Hu ◽  
Yinghua Zhang ◽  
Yukun Gao ◽  
...  

1993 ◽  
Vol 34 (52) ◽  
pp. 8509-8512 ◽  
Author(s):  
Takashi Ohshima ◽  
Mikiko Sodeoka ◽  
Masakatsu Shibasaki

2019 ◽  
Author(s):  
Brian Pinkard ◽  
John Kramlich ◽  
Igor V. Novosselov

<div> <p></p><p>Supercritical water gasification is a promising waste-to-energy technology with the ability to convert aqueous and/or heterogeneous organic feedstocks to high-value gaseous products. Reaction behavior of complex molecules in supercritical water can be inferred through knowledge of the reaction pathways of model compounds in supercritical water. In this study methanol, ethanol, and isopropyl alcohol are gasified in a continuous supercritical water reactor at temperatures between 500 and 560 °C, and for residence times between 3 and 8 s. <i>In situ</i> Raman spectroscopy is used to rapidly identify and quantify reaction products. The results suggest the dominance of chain-branching, free radical reaction mechanisms that are responsible for decomposing primary alcohols in the supercritical water environment. The presence of a catalytic surface is proposed to be highly significant for initiating radical reactions. Global reaction pathways are proposed, and mechanisms for free radical reaction initiation, propagation, and termination are discussed in light of these and previously published experimental results.</p><br><p></p></div>


2019 ◽  
Author(s):  
Brian Pinkard ◽  
John Kramlich ◽  
Igor V. Novosselov

<div> <p></p><p>Supercritical water gasification is a promising waste-to-energy technology with the ability to convert aqueous and/or heterogeneous organic feedstocks to high-value gaseous products. Reaction behavior of complex molecules in supercritical water can be inferred through knowledge of the reaction pathways of model compounds in supercritical water. In this study methanol, ethanol, and isopropyl alcohol are gasified in a continuous supercritical water reactor at temperatures between 500 and 560 °C, and for residence times between 3 and 8 s. <i>In situ</i> Raman spectroscopy is used to rapidly identify and quantify reaction products. The results suggest the dominance of chain-branching, free radical reaction mechanisms that are responsible for decomposing primary alcohols in the supercritical water environment. The presence of a catalytic surface is proposed to be highly significant for initiating radical reactions. Global reaction pathways are proposed, and mechanisms for free radical reaction initiation, propagation, and termination are discussed in light of these and previously published experimental results.</p><br><p></p></div>


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