Acid/hydrazide-appended covalent triazine frameworks for low-pressure CO2 capture: pre-designable or post-synthesis modification. Issue 40 (29th September 2017)
- Record Type:
- Journal Article
- Title:
- Acid/hydrazide-appended covalent triazine frameworks for low-pressure CO2 capture: pre-designable or post-synthesis modification. Issue 40 (29th September 2017)
- Main Title:
- Acid/hydrazide-appended covalent triazine frameworks for low-pressure CO2 capture: pre-designable or post-synthesis modification
- Authors:
- Fu, Yu
Wang, Zhiqiang
Fu, Xianbiao
Yan, Jun
Liu, Cheng
Pan, Chunyue
Yu, Guipeng - Abstract:
- Abstract : Pore surface engineering in nanoporous organic polymers (NOPs) targeted for their different applications remains a critical challenge. Abstract : Pore surface engineering in nanoporous organic polymers (NOPs) targeted for their different applications remains a critical challenge. Here we compare two classic modification strategies, i.e. pre-designable and post-synthesis modification, which allow controlled loading of functionalities onto the pore wall by anchoring ethyl ester, acetic acid or acetohydrazides for effective CO2 capture. The pre-designed acetic acid-appended or acetohydrazide-appended precursors permit the construction of covalent triazine frameworks (CTF-CSU36@pre and CTF-CSU37@pre) with walls to which an exciting content of functional units is anchored. Conversely, channel functionalization is made possible by facile hydrolysis or hydrazide reaction of a carbazole-bridged triazine framework with pendant ethyl ester (CTF-CSU20) to produce surfaces with desired acetic acid (CTF-CSU36@post) or acetohydrazide groups (CTF-CSU37@post). High-degree dense integration of functional groups on the channel walls proved the superiority of the post-synthesis modification relative to the pre-designable strategy. Porous monoliths with high capacity at very low pressures (5.7 wt% at 273 K/0.15 bar), excellent IAST ideal selectivity (CO2 /N2 = 145.9) and reusability were created, demonstrating their great potential for gas storage and separation. Significantly, suchAbstract : Pore surface engineering in nanoporous organic polymers (NOPs) targeted for their different applications remains a critical challenge. Abstract : Pore surface engineering in nanoporous organic polymers (NOPs) targeted for their different applications remains a critical challenge. Here we compare two classic modification strategies, i.e. pre-designable and post-synthesis modification, which allow controlled loading of functionalities onto the pore wall by anchoring ethyl ester, acetic acid or acetohydrazides for effective CO2 capture. The pre-designed acetic acid-appended or acetohydrazide-appended precursors permit the construction of covalent triazine frameworks (CTF-CSU36@pre and CTF-CSU37@pre) with walls to which an exciting content of functional units is anchored. Conversely, channel functionalization is made possible by facile hydrolysis or hydrazide reaction of a carbazole-bridged triazine framework with pendant ethyl ester (CTF-CSU20) to produce surfaces with desired acetic acid (CTF-CSU36@post) or acetohydrazide groups (CTF-CSU37@post). High-degree dense integration of functional groups on the channel walls proved the superiority of the post-synthesis modification relative to the pre-designable strategy. Porous monoliths with high capacity at very low pressures (5.7 wt% at 273 K/0.15 bar), excellent IAST ideal selectivity (CO2 /N2 = 145.9) and reusability were created, demonstrating their great potential for gas storage and separation. Significantly, such tailor-made pore-wall functional engineering could be a facile and powerful strategy for broad applications of NOPs. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 5:Issue 40(2017)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 5:Issue 40(2017)
- Issue Display:
- Volume 5, Issue 40 (2017)
- Year:
- 2017
- Volume:
- 5
- Issue:
- 40
- Issue Sort Value:
- 2017-0005-0040-0000
- Page Start:
- 21266
- Page End:
- 21274
- Publication Date:
- 2017-09-29
- Subjects:
- Materials -- Research -- Periodicals
Chemistry, Analytic -- Periodicals
Environmental sciences -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ta ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7ta05416e ↗
- Languages:
- English
- ISSNs:
- 2050-7488
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205100
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5117.xml