An overview on trace CO2 removal by advanced physisorbent materials.

Abstract:

:This review paper focuses on various gas processing technologies and materials that efficiently capture trace levels of carbon dioxide (CO2). Fundamental separation mechanisms such as absorption, adsorption, and distillation technology are presented. Liquid amine-based carbon capture (C-capture) technologies have been in existence for over half a century, however, liquid amine capture relies upon chemical reactions and is energy-intensive. Liquid amines are thus not economically viable for broad deployment and offer little room for innovation. Innovative C-capture technologies must improve both the environmental footprint and cost-effectiveness. As a promising alternative, physisorbents have many advantages including considerably lower regeneration energy. Generally, existing classes of physisorbent materials, such as metal-organic frameworks (MOFs) and zeolites are selective toward C-capture. However, their selectivity is currently not high enough to remove trace levels (e.g., ~1%) of CO2 from various natural gas process streams. This review summarizes the current advancements in physisorbent materials for CO2 capture. Here, key performance parameters needed to select the most suitable candidate are highlighted. Furthermore, this review discusses the scope for the development of better performing CO2 selective physisorbents from both environmental and economic perspectives. In addition, hybrid ultra microporous materials (HUMs), characterized mainly by ultra-micro pores (<0.7 nm), are discussed in reference to C-capture. Various characteristics of HUMs result in high selectivity and applicability in difficult separations such as the gas sweetening and C-capture from complex humid mixed gas streams.

journal_name

J Environ Manage

authors

Khraisheh M,Mukherjee S,Kumar A,Al Momani F,Walker G,Zaworotko MJ

doi

10.1016/j.jenvman.2019.109874

subject

Has Abstract

pub_date

2020-02-01 00:00:00

pages

109874

eissn

0301-4797

issn

1095-8630

pii

S0301-4797(19)31592-0

journal_volume

255

pub_type

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