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Direct Air Capture of CO(2) Using Amine/Alumina Sorbents at Cold Temperature

[Image: see text] Rising CO(2) emissions are responsible for increasing global temperatures causing climate change. Significant efforts are underway to develop amine-based sorbents to directly capture CO(2) from air (called direct air capture (DAC)) to combat the effects of climate change. However,...

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Detalles Bibliográficos
Autores principales: Priyadarshini, Pranjali, Rim, Guanhe, Rosu, Cornelia, Song, MinGyu, Jones, Christopher W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515709/
https://www.ncbi.nlm.nih.gov/pubmed/37743951
http://dx.doi.org/10.1021/acsenvironau.3c00010
Descripción
Sumario:[Image: see text] Rising CO(2) emissions are responsible for increasing global temperatures causing climate change. Significant efforts are underway to develop amine-based sorbents to directly capture CO(2) from air (called direct air capture (DAC)) to combat the effects of climate change. However, the sorbents’ performances have usually been evaluated at ambient temperatures (25 °C) or higher, most often under dry conditions. A significant portion of the natural environment where DAC plants can be deployed experiences temperatures below 25 °C, and ambient air always contains some humidity. In this study, we assess the CO(2) adsorption behavior of amine (poly(ethyleneimine) (PEI) and tetraethylenepentamine (TEPA)) impregnated into porous alumina at ambient (25 °C) and cold temperatures (−20 °C) under dry and humid conditions. CO(2) adsorption capacities at 25 °C and 400 ppm CO(2) are highest for 40 wt% TEPA-incorporated γ-Al(2)O(3) samples (1.8 mmol CO(2)/g sorbent), while 40 wt % PEI-impregnated γ-Al(2)O(3) samples exhibit moderate uptakes (0.9 mmol g(–1)). CO(2) capacities for both PEI- and TEPA-incorporated γ-Al(2)O(3) samples decrease with decreasing amine content and temperatures. The 40 and 20 wt % TEPA sorbents show the best performance at −20 °C under dry conditions (1.6 and 1.1 mmol g(–1), respectively). Both the TEPA samples also exhibit stable and high working capacities (0.9 and 1.2 mmol g(–1)) across 10 cycles of adsorption–desorption (adsorption at −20 °C and desorption conducted at 60 °C). Introducing moisture (70% RH at −20 and 25 °C) improves the CO(2) capacity of the amine-impregnated sorbents at both temperatures. The 40 wt% PEI, 40 wt % TEPA, and 20 wt% TEPA samples show good CO(2) uptakes at both temperatures. The results presented here indicate that γ-Al(2)O(3) impregnated with PEI and TEPA are potential materials for DAC at ambient and cold conditions, with further opportunities to optimize these materials for the scalable deployment of DAC plants at different environmental conditions.