Efficient removal of bisphenol pollutants on imine-based covalent organic frameworks: adsorption behavior and mechanism. Issue 30 (20th May 2021)
- Record Type:
- Journal Article
- Title:
- Efficient removal of bisphenol pollutants on imine-based covalent organic frameworks: adsorption behavior and mechanism. Issue 30 (20th May 2021)
- Main Title:
- Efficient removal of bisphenol pollutants on imine-based covalent organic frameworks: adsorption behavior and mechanism
- Authors:
- Fu, Daijun
Zhang, Qianxin
Chen, Ping
Zheng, Xiaoshan
Hao, Jun
Mo, Peiying
Liu, Haijin
Liu, Guoguang
Lv, Wenying - Abstract:
- Abstract : Two imine-based covalent organic frameworks with different pore sizes were synthesized, and can be used as adsorbents for the removal of bisphenol pollutants, showing high affinity toward bisphenol S and bisphenol A. Abstract : The extensive use of bisphenol analogues in industry has aggravated the contamination of the water environment, and how to effectively remove them has become a research hotspot. This study presents two imine-based covalent organic frameworks with different pore sizes (COFs) [TAPB (1, 3, 5-tris(4-aminophenyl)benzene)-Dva (2, 5-divinylterephthaldehyde)-PDA (terephthalaldehyde) (COF-1), and TAPB (1, 3, 5-tris(4-aminophenyl)benzene)-Dva (2, 5-divinylterephthaldehyde)-BPDA (biphenyl dialdehyde) (COF-2)], which have achieved the efficient adsorption of bisphenol S (BPS) and bisphenol A (BPA). The maximum adsorption capacity of COF-2 for BPS and BPA obtained from Langmuir isotherms were calculated as 200.00 mg g −1 and 149.25 mg g −1 . Both hydrogen bonding and π–π interactions might have been responsible for the adsorption of BPS and BPA on the COFs, where the high adsorption capacity of COFs was due to their unique pore dimensions and structures. Different types of pharmaceutical adsorption studies indicated that COF-2 exhibited a higher adsorption performance for different types of pharmaceuticals than COF-1, and the adsorption capacity was ranked as follows: bisphenol pharmaceuticals > anti-inflammatory pharmaceuticals > sulfa pharmaceuticals.Abstract : Two imine-based covalent organic frameworks with different pore sizes were synthesized, and can be used as adsorbents for the removal of bisphenol pollutants, showing high affinity toward bisphenol S and bisphenol A. Abstract : The extensive use of bisphenol analogues in industry has aggravated the contamination of the water environment, and how to effectively remove them has become a research hotspot. This study presents two imine-based covalent organic frameworks with different pore sizes (COFs) [TAPB (1, 3, 5-tris(4-aminophenyl)benzene)-Dva (2, 5-divinylterephthaldehyde)-PDA (terephthalaldehyde) (COF-1), and TAPB (1, 3, 5-tris(4-aminophenyl)benzene)-Dva (2, 5-divinylterephthaldehyde)-BPDA (biphenyl dialdehyde) (COF-2)], which have achieved the efficient adsorption of bisphenol S (BPS) and bisphenol A (BPA). The maximum adsorption capacity of COF-2 for BPS and BPA obtained from Langmuir isotherms were calculated as 200.00 mg g −1 and 149.25 mg g −1 . Both hydrogen bonding and π–π interactions might have been responsible for the adsorption of BPS and BPA on the COFs, where the high adsorption capacity of COFs was due to their unique pore dimensions and structures. Different types of pharmaceutical adsorption studies indicated that COF-2 exhibited a higher adsorption performance for different types of pharmaceuticals than COF-1, and the adsorption capacity was ranked as follows: bisphenol pharmaceuticals > anti-inflammatory pharmaceuticals > sulfa pharmaceuticals. These results confirmed that COFs with larger pore sizes were more conducive to the adsorption of pollutants with smaller molecular dimensions. Moreover, COF-1 and COF-2 possessed excellent pH stability and recyclability, which suggested strong potential applications for these novel adsorbents in the remediation of organic pollutants in natural waterways and aqueous ecosystems. … (more)
- Is Part Of:
- RSC advances. Volume 11:Issue 30(2021)
- Journal:
- RSC advances
- Issue:
- Volume 11:Issue 30(2021)
- Issue Display:
- Volume 11, Issue 30 (2021)
- Year:
- 2021
- Volume:
- 11
- Issue:
- 30
- Issue Sort Value:
- 2021-0011-0030-0000
- Page Start:
- 18308
- Page End:
- 18320
- Publication Date:
- 2021-05-20
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1ra02342j ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 16888.xml