The platform will undergo maintenance on Sep 14 at about 7:45 AM EST and will be unavailable for approximately 2 hours.
2020
DOI: 10.1016/j.ijggc.2020.103005
|View full text |Cite
|
Sign up to set email alerts
|

CO2 capture adsorbents functionalized by amine – bearing polymers: A review

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

4
168
0
1

Year Published

2020
2020
2022
2022

Publication Types

Select...
6
1
1
1

Relationship

1
8

Authors

Journals

citations
Cited by 221 publications
(173 citation statements)
references
References 301 publications
4
168
0
1
Order By: Relevance
“…Thus, a range of nucleophilic reagents, including neutral N -heterocyclic carbenes [ 25 , 26 ], are known to react with CO 2 even under mild conditions, and some chemistry at transition metal centers is provided by the possibility of CO 2 insertion into the bond between a metal atom and a suitable anionic ligand, e.g., alkyl, allyl, alkoxide and hydride [ 27 , 28 , 29 , 30 , 31 , 32 ]. In this context, amines are key reactants towards carbon dioxide, and indeed carbon dioxide/amine systems have been intensively investigated in the field of capture/storage [ 33 , 34 , 35 ] and exploited for the incorporation of the CO 2 moiety within organic structures [ 36 , 37 , 38 , 39 ]. Furthermore, CO 2 is also prone to insertion reactions into a variety of metal-amide bonds, generating a carbamato ligand; however, metal complexes containing carbamato ligands are easily available through diverse synthetic routes not requiring the use of pressurized CO 2 .…”
Section: Introductionmentioning
confidence: 99%
“…Thus, a range of nucleophilic reagents, including neutral N -heterocyclic carbenes [ 25 , 26 ], are known to react with CO 2 even under mild conditions, and some chemistry at transition metal centers is provided by the possibility of CO 2 insertion into the bond between a metal atom and a suitable anionic ligand, e.g., alkyl, allyl, alkoxide and hydride [ 27 , 28 , 29 , 30 , 31 , 32 ]. In this context, amines are key reactants towards carbon dioxide, and indeed carbon dioxide/amine systems have been intensively investigated in the field of capture/storage [ 33 , 34 , 35 ] and exploited for the incorporation of the CO 2 moiety within organic structures [ 36 , 37 , 38 , 39 ]. Furthermore, CO 2 is also prone to insertion reactions into a variety of metal-amide bonds, generating a carbamato ligand; however, metal complexes containing carbamato ligands are easily available through diverse synthetic routes not requiring the use of pressurized CO 2 .…”
Section: Introductionmentioning
confidence: 99%
“…The amount of amine grafted onto a support depends on the density of the appropriate silanol groups. Hence, on the way to optimize amine-grafted materials for CO 2 capture, the main efforts are focused on increasing the number of amine functional groups per unit of support area, enhancing CO 2 -phylicity of the amines, and, finally, increasing the CO 2 capacity [19].…”
Section: Materials For Chemical Co 2 Adsorptionmentioning
confidence: 99%
“…For more detailed information concerning solid adsorbents functionalized by amines, we would recommend Ref. [19] and the closely related references therein.…”
Section: Materials For Chemical Co 2 Adsorptionmentioning
confidence: 99%
“…Within the area of carbon dioxide capture, liquid amines have seen the most use at scale in pilot plants designed to reversibly capture CO2 and yielding a purified stream of CO2 for subsequent sequestration [18], [21]- [23]. However, amines and especially their regeneration incur a relatively high energy cost, and there exist concerns regarding their toxicity [24], motivating research over the past two decades to develop alternative materials.…”
Section: Introduction and Objectives -Co2 Capture By Metal Oxidesmentioning
confidence: 99%