کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
150181 456446 2012 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Characterization and kinetics of carbon dioxide absorption into aqueous tetramethylammonium glycinate solution
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
Characterization and kinetics of carbon dioxide absorption into aqueous tetramethylammonium glycinate solution
چکیده انگلیسی

An advanced aqueous amine solvent of tetramethylammonium glycinate ([N1 1 1 1][Gly]) was characterized for carbon dioxide (CO2) absorption purposes. Density, viscosity and pH of the [N1 1 1 1][Gly] solution, with concentrations ranging from 5% to 30%, were determined at temperatures from 298 to 323 K. Solubility and diffusivity of CO2 in [N1 1 1 1][Gly] solution at the same temperatures and concentrations was estimated. Absorption of CO2 into [N1 1 1 1][Gly] aqueous solution was investigated using a double stirred-cell absorber with a planar gas–liquid interface. The effects of the [N1 1 1 1][Gly] concentration, temperature and CO2 concentration of absorption CO2 into aqueous [N1 1 1 1][Gly] were studied. The kinetics study showed that absorption CO2 into aqueous [N1 1 1 1][Gly] was the fast pseudo-first order reaction regime. Based on the reaction regime, the enhancement factor E, the overall reaction kinetic constant kov and the second-order rate constant k2 were obtained using the two-film model. The results showed that E was linear with CB01/2, and the activation energy of 15% aqueous [N1 1 1 1][Gly] absorbing CO2 was 15.431 kJ mol−1.


► Low concentration of [N1 1 1 1][Gly] aqueous solution was favorable for CO2 absorption.
► [N1 1 1 1][Gly] aqueous solution was characterized for CO2 absorption purpose.
► [N1 1 1 1][Gly] aqueous solution absorbing CO2 was the fast pseudo-first order reaction.
► Enhancement factor was linear with square root of [N1 1 1 1][Gly] initial concentration.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemical Engineering Journal - Volumes 181–182, 1 February 2012, Pages 85–92
نویسندگان
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