Chlorination in Combustion Systems

2000 ◽  
Author(s):  
Wing Tsang ◽  
Valeri Babushok

Abstract This paper is concerned with the formation of polychorinated organics in the gas phase in combustion systems. The results are derived from simulation studies with inputs from the fundamental kinetics of single step thermal gas phase reactions. Attention is focussed on the case where initial chlorine loading is low. It is shown that in a well mixed system high degrees of chlorination are difficult to attain due to the decrease in thermal stability with chlorination. A hypothesis for their formation as a consequence of chlorine formation during lean combustion followed by chlorination of organics as a result of the mixing and quenching of the products from rich combustion is tested. Under such conditions the competition between oxidation and chlorination of intermediates governs the final product distribution. The stability of propargyl radicals (C3H3) to oxidation makes chlorination of its products a preferred mode and results have been obtained where more highly chlorinated compounds are found in the products. Since this radical is a known precursor to benzene formation, this provides a direct route for the formation of polychlorinated benzenes. The scenario presented here extends regions for possible gas phase chlorination into the exhaust system of combustors.




2001 ◽  
Vol 124 (4) ◽  
pp. 573-589 ◽  
Author(s):  
K.J Hughes ◽  
A.S Tomlin ◽  
E Hampartsoumian ◽  
W Nimmo ◽  
I.G Zsély ◽  
...  


Author(s):  
Victor N. Kondratiev ◽  
Evgeniĭ E. Nikitin


Author(s):  
Jonathan R. Church ◽  
Veronica Vaida ◽  
Rex T. Skodje


2012 ◽  
Vol 1 (1) ◽  
pp. P46-P53 ◽  
Author(s):  
Ran Zuo ◽  
Haiqun Yu ◽  
Nan Xu ◽  
Xiaokun He


Holzforschung ◽  
2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Ajinkya More ◽  
Thomas Elder ◽  
Zhihua Jiang

Abstract This review discusses the main factors that govern the oxidation processes of lignins into aromatic aldehydes and acids using hydrogen peroxide. Aromatic aldehydes and acids are produced in the oxidative degradation of lignin whereas mono and dicarboxylic acids are the main products. The stability of hydrogen peroxide under the reaction conditions is an important factor that needs to be addressed for selectively improving the yield of aromatic aldehydes. Hydrogen peroxide in the presence of heavy metal ions readily decomposes, leading to minor degradation of lignin. This degradation results in quinones which are highly reactive towards peroxide. Under these reaction conditions, the pH of the reaction medium defines the reaction mechanism and the product distribution. Under acidic conditions, hydrogen peroxide reacts electrophilically with electron rich aromatic and olefinic structures at comparatively higher temperatures. In contrast, under alkaline conditions it reacts nucleophilically with electron deficient carbonyl and conjugated carbonyl structures in lignin. The reaction pattern in the oxidation of lignin usually involves cleavage of the aromatic ring, the aliphatic side chain or other linkages which will be discussed in this review.



1957 ◽  
Vol 79 (17) ◽  
pp. 4609-4616 ◽  
Author(s):  
Adon A. Gordus ◽  
John E. Willard




1993 ◽  
Vol 168 (2) ◽  
pp. 177-181 ◽  
Author(s):  
E Borsella ◽  
S Botti ◽  
R Alexandrescu ◽  
I Morjan ◽  
T Dikonimos-Makris ◽  
...  


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