Decomposition of Potassium Hydrogen Carbonate: Thermochemistry, Kinetics, and Textural Changes in Solids

被引:25
|
作者
Hartman, Miloslav [1 ,2 ]
Svoboda, Karel [1 ,3 ]
Cech, Bohumir [2 ]
Pohorely, Michael [1 ,4 ]
Syc, Michal [1 ]
机构
[1] AS CR, Inst Chem Proc Fundamentals, Rozvojova 135, Prague 16502 6, Czech Republic
[2] Tech Univ Ostrava, ENET Ctr, 17,Listopadu 15, Ostrava 70833, Czech Republic
[3] Univ Jan Evangelista Purkyne, Fac Environm, Kralova Vysina 7, Usti Nad Labem 40096, Czech Republic
[4] Univ Chem & Technol Prague, Dept Power Engn, Tech 5, Prague 16628 6, Czech Republic
关键词
THERMAL-DECOMPOSITION; SODIUM-CARBONATE; SULFUR-DIOXIDE; FLUIDIZED-BED; DISSOCIATION PRESSURES; ALKALI BICARBONATES; SURFACE-AREA; GAS; GASIFICATION; PARAMETERS;
D O I
10.1021/acs.iecr.8b06151
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
To determine unbiased rates of the decomposition of KHCO3, slowly increasing- and constant-temperature TGA methods were employed with small, finely ground samples. Such reaction provides a novel, porous, and highly reactive sorbent for noxious and/or malodorous gases. The bicarbonate commences decomposing at 364 K, and the maximum rate of reaction, attained at 421.9 K, amounts to 5.73 x 10(-4) 1/s. Taking advantage of the Schlomilch function, an Arrhenius-type relationship is developed by an integral method: the activation energy is as large as 141.3 kJ/mol and the order of reaction amounts to 1.145. While the pore volume made by calcination (0.2309 cm(3)/g) is not affected by temperature at 403-503 K, the mean pore diameter and the grain size augment with increasing temperature. The diagram presented makes it possible to conveniently predict the conditions to attain near-complete conversion of the bicarbonate and minimize undesirable sintering of the nascent carbonate.
引用
收藏
页码:2868 / 2881
页数:14
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