Reaction of NO and N2O gases with graphite in TGA

被引:0
作者
Young-Cheol Bak
机构
[1] Gyeongsang National University,Department of Chemical Engineering/Research Institute of Industrial Technology
来源
Korean Journal of Chemical Engineering | 1998年 / 15卷
关键词
Nitric Oxide; Nitrous Oxide; Graphite; TGA; Isothermal Reaction;
D O I
暂无
中图分类号
学科分类号
摘要
Thermal analyses were conducted in a thermogravimetric analyzer by isothermal techniques in order to characterize the carbon-nitrogen oxide reaction. The carbon samples employed in the present study were SP-1 graphite and Micro 450 graphite. Carbon-NO and carbon-N2O reactions were carried out in a temperature range of 550–900 °C and 5–20 kPa of the partial pressure of reactant. In the NO reaction, reaction orders with respect to NO concentration and activation energy were 0.46-0.92 and 85–102 kJ/mol, respectively. The rate on the monolayer edge was higher than the rate on the multilayer edges. In the N2O reaction, reaction orders with respect to N2O concentration and activation energy were 0.55–1.35 and 167–190 kJ/mol, respectively.
引用
收藏
页码:336 / 340
页数:4
相关论文
共 63 条
[1]  
Aama I.(1997)A Review of the Kinetics of the Nitric Oxide-Carbon Reaction Fuel 76 475-475
[2]  
Suuberg M.(1991)Partitioning of Nitrogenous Species in the Fuel-Rich Stage of Reburning Energy & Fuels 5 231-231
[3]  
Burch T. E.(1983)Kinetics of the NO-Carbon Reaction at Fluidized-Bed Combustor Conditions Combustion and Flame 52 37-37
[4]  
Tillman F. R.(1993)Titration for Basal Plane versus Edge Plane Surface on Graphite Carbons by Adsorption Langmuir 9 3259-3259
[5]  
Chen W.(1996)Effect of Heterogeneous Mechanisms during Reburning of NO AIChE 42 1968-1968
[6]  
Lester T. W.(1993)Intrinsic Rates of NO Ind. Eng. Chem. Res. 32 1359-1359
[7]  
Conway R. B.(1991)-Carbon Reactions Carbon 29 179-179
[8]  
Sterling A. M.(1996)Gasification of Cellulosic Chars in Oxygen and in NO Energy & Fuel 10 203-203
[9]  
Chan L. K.(1985)Mechanisms of N Fuel 64 1306-1306
[10]  
Sarofim A. F.(1997)O Formation from Char Combustion Korean J. Chem. Eng. 14 491-491