US EPA

7445911 

Journal Article 

Effects of Transition Metal Oxide Catalysts on MEA Solvent Regeneration for the Post-Combustion Carbon Capture Process 

Bhatti, UH; Shah, AK; Kim, J; You, JK; Choi, S; Lim, D; Nam, S; Park, YHo; Baek, IlH 

2017 

ACS Sustainable Chemistry & Engineering
ISSN: 2168-0485 

American Chemical Society 

5 

7 

5862-5868 

English 

10.1021/acssuschemeng.7b00604 

WOS:000405139100030 

Large heat duty for amine regeneration in absorption-based CO2 capture is one of the major drawbacks of this process. Along with a highly endothermic carbamate breakdown reaction in the stripper, the difficulty of proton transfer from protonated amines to water in the amine regeneration process is also considered a basic reason for high heat duty. Transition metal oxide catalysts can play a vital role in decreasing the required thermal energy for amine regeneration in the stripper by providing Bronsted acids and Lewis acids that would help break down the carbamate by direct attack. MEA saturated with CO2 at 35 °C, with initial loading of 0.56 mole CO2/mole amine, was used in this study. The performance of five different transition metal oxide catalysts, V2O5, MoO3, WO3, TiO2, and Cr2O3, was studied separately to investigate the effects of these catalysts on amine regeneration in the temperature range of 35-86 °C. It has been observed that MoO3 performance is much better as it regenerated almost double of the MEA solvent than noncatalytic amine regeneration systems, whereas other catalysts also showed considerable differences in amine regeneration in this temperature range. The amine regeneration performance trend was MoO3 > V2O5 > Cr2O3 > TiO2 > WO3 > blank test. The application of this work would mean that metal oxide catalysts could be used in strippers for a faster CO2 desorption rate at lower temperature, which would cause a significant reduction of the heat duty. © 2017 American Chemical Society. 

Catalytic amine regeneration; MEA; Post-combustion CO2 capture; Transition metal oxides; Bronsted and Lewis acid sites