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HERO ID
7543603
Reference Type
Journal Article
Title
Sterically Hindered Amines for CO2 Removal from Gases
Author(s)
Sartorl, G; Savage, DW
Year
1983
Is Peer Reviewed?
0
Journal
Industrial and Engineering Chemistry Fundamentals
ISSN:
0196-4313
Publisher
AMER CHEMICAL SOC
Location
WASHINGTON
Volume
22
Issue
2
Page Numbers
239-249
Language
English
DOI
10.1021/i100010a016
Web of Science Id
WOS:A1983QM07300016
Abstract
Steric hindrance and basicity are shown to control CO2-amine reactions. In aqueous amino alcohols, steric hindrance is the dominant factor giving high thermodynamic capacity and fast absorption rates at high CO2 loadings. Introducing steric hindrance by a bulky substituent adjacent to the amino group lowers the stability of the carbamate formed by CO2-amine reaction. Reduced carbamate stability allows thermodynamic CO2 loadings to exceed those attainable with conventional, stable-carbamate amines. Lowering carbamate stability also leads to high free-amine concentration in solution; therefore fast amine-CO2 reaction rates are obtained despite some reduction of the rate constant owing to steric interference. Hindered amines show capacity and absorption rate advantages over conventional amines for CO2 removal from gases by absorption in aqueous amine solutions and amine-promoted hot potassium carbonate. Cyclic capacity broadening of 20-40% and absorption rate increases up to 100% or more are possible with certain hindered amines. © 1983, American Chemical Society. All rights reserved.
Keywords
CHEMICAL REACTIONS; THERMODYNAMICS; AMINES; CARBAMATE; STERIC HINDRANCE; CARBON DIOXIDE
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