Cargando…

Direct Air Capture of CO(2) Using a Liquid Amine–Solid Carbamic Acid Phase-Separation System Using Diamines Bearing an Aminocyclohexyl Group

[Image: see text] The phase separation between a liquid amine and the solid carbamic acid exhibited >99% CO(2) removal efficiency under a 400 ppm CO(2) flow system using diamines bearing an aminocyclohexyl group. Among them, isophorone diamine [IPDA; 3-(aminomethyl)-3,5,5-trimethylcyclohexylamine...

Descripción completa

Detalles Bibliográficos
Autores principales: Kikkawa, Soichi, Amamoto, Kazushi, Fujiki, Yu, Hirayama, Jun, Kato, Gen, Miura, Hiroki, Shishido, Tetsuya, Yamazoe, Seiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10125313/
https://www.ncbi.nlm.nih.gov/pubmed/37101968
http://dx.doi.org/10.1021/acsenvironau.1c00065
_version_ 1785030001164288000
author Kikkawa, Soichi
Amamoto, Kazushi
Fujiki, Yu
Hirayama, Jun
Kato, Gen
Miura, Hiroki
Shishido, Tetsuya
Yamazoe, Seiji
author_facet Kikkawa, Soichi
Amamoto, Kazushi
Fujiki, Yu
Hirayama, Jun
Kato, Gen
Miura, Hiroki
Shishido, Tetsuya
Yamazoe, Seiji
author_sort Kikkawa, Soichi
collection PubMed
description [Image: see text] The phase separation between a liquid amine and the solid carbamic acid exhibited >99% CO(2) removal efficiency under a 400 ppm CO(2) flow system using diamines bearing an aminocyclohexyl group. Among them, isophorone diamine [IPDA; 3-(aminomethyl)-3,5,5-trimethylcyclohexylamine] exhibited the highest CO(2) removal efficiency. IPDA reacted with CO(2) in a CO(2)/IPDA molar ratio of ≥1 even in H(2)O as a solvent. The captured CO(2) was completely desorbed at 333 K because the dissolved carbamate ion releases CO(2) at low temperatures. The reusability of IPDA under CO(2) adsorption-and-desorption cycles without degradation, the >99% efficiency kept for 100 h under direct air capture conditions, and the high CO(2) capture rate (201 mmol/h for 1 mol of amine) suggest that the phase separation system using IPDA is robust and durable for practical use.
format Online
Article
Text
id pubmed-10125313
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-101253132023-04-25 Direct Air Capture of CO(2) Using a Liquid Amine–Solid Carbamic Acid Phase-Separation System Using Diamines Bearing an Aminocyclohexyl Group Kikkawa, Soichi Amamoto, Kazushi Fujiki, Yu Hirayama, Jun Kato, Gen Miura, Hiroki Shishido, Tetsuya Yamazoe, Seiji ACS Environ Au [Image: see text] The phase separation between a liquid amine and the solid carbamic acid exhibited >99% CO(2) removal efficiency under a 400 ppm CO(2) flow system using diamines bearing an aminocyclohexyl group. Among them, isophorone diamine [IPDA; 3-(aminomethyl)-3,5,5-trimethylcyclohexylamine] exhibited the highest CO(2) removal efficiency. IPDA reacted with CO(2) in a CO(2)/IPDA molar ratio of ≥1 even in H(2)O as a solvent. The captured CO(2) was completely desorbed at 333 K because the dissolved carbamate ion releases CO(2) at low temperatures. The reusability of IPDA under CO(2) adsorption-and-desorption cycles without degradation, the >99% efficiency kept for 100 h under direct air capture conditions, and the high CO(2) capture rate (201 mmol/h for 1 mol of amine) suggest that the phase separation system using IPDA is robust and durable for practical use. American Chemical Society 2022-05-10 /pmc/articles/PMC10125313/ /pubmed/37101968 http://dx.doi.org/10.1021/acsenvironau.1c00065 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Kikkawa, Soichi
Amamoto, Kazushi
Fujiki, Yu
Hirayama, Jun
Kato, Gen
Miura, Hiroki
Shishido, Tetsuya
Yamazoe, Seiji
Direct Air Capture of CO(2) Using a Liquid Amine–Solid Carbamic Acid Phase-Separation System Using Diamines Bearing an Aminocyclohexyl Group
title Direct Air Capture of CO(2) Using a Liquid Amine–Solid Carbamic Acid Phase-Separation System Using Diamines Bearing an Aminocyclohexyl Group
title_full Direct Air Capture of CO(2) Using a Liquid Amine–Solid Carbamic Acid Phase-Separation System Using Diamines Bearing an Aminocyclohexyl Group
title_fullStr Direct Air Capture of CO(2) Using a Liquid Amine–Solid Carbamic Acid Phase-Separation System Using Diamines Bearing an Aminocyclohexyl Group
title_full_unstemmed Direct Air Capture of CO(2) Using a Liquid Amine–Solid Carbamic Acid Phase-Separation System Using Diamines Bearing an Aminocyclohexyl Group
title_short Direct Air Capture of CO(2) Using a Liquid Amine–Solid Carbamic Acid Phase-Separation System Using Diamines Bearing an Aminocyclohexyl Group
title_sort direct air capture of co(2) using a liquid amine–solid carbamic acid phase-separation system using diamines bearing an aminocyclohexyl group
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10125313/
https://www.ncbi.nlm.nih.gov/pubmed/37101968
http://dx.doi.org/10.1021/acsenvironau.1c00065
work_keys_str_mv AT kikkawasoichi directaircaptureofco2usingaliquidaminesolidcarbamicacidphaseseparationsystemusingdiaminesbearinganaminocyclohexylgroup
AT amamotokazushi directaircaptureofco2usingaliquidaminesolidcarbamicacidphaseseparationsystemusingdiaminesbearinganaminocyclohexylgroup
AT fujikiyu directaircaptureofco2usingaliquidaminesolidcarbamicacidphaseseparationsystemusingdiaminesbearinganaminocyclohexylgroup
AT hirayamajun directaircaptureofco2usingaliquidaminesolidcarbamicacidphaseseparationsystemusingdiaminesbearinganaminocyclohexylgroup
AT katogen directaircaptureofco2usingaliquidaminesolidcarbamicacidphaseseparationsystemusingdiaminesbearinganaminocyclohexylgroup
AT miurahiroki directaircaptureofco2usingaliquidaminesolidcarbamicacidphaseseparationsystemusingdiaminesbearinganaminocyclohexylgroup
AT shishidotetsuya directaircaptureofco2usingaliquidaminesolidcarbamicacidphaseseparationsystemusingdiaminesbearinganaminocyclohexylgroup
AT yamazoeseiji directaircaptureofco2usingaliquidaminesolidcarbamicacidphaseseparationsystemusingdiaminesbearinganaminocyclohexylgroup