A Robust Salty Water Adhesive by Counterion Exchange Induced Coacervate. Issue 7 (23rd January 2019)
- Record Type:
- Journal Article
- Title:
- A Robust Salty Water Adhesive by Counterion Exchange Induced Coacervate. Issue 7 (23rd January 2019)
- Main Title:
- A Robust Salty Water Adhesive by Counterion Exchange Induced Coacervate
- Authors:
- Zhu, Xiangwei
Wei, Congying
Zhang, Fang
Tang, Qingquan
Zhao, Qiang - Abstract:
- Abstract: Counterion exchange of charged macromolecules has comprehensive implications in biological and synthetic systems such as protein function, biosignaling, ion conducting, and separation, but the correlation between the dynamic ion exchange, polyelectrolyte phase separation, and functionality remains elusive. Here, counterion exchange is exploited as a means to facilitate liquid–liquid phase separation and coacervates featuring higher stability and versatility compared with conventional complex coacervate. Self‐coacervation of a cationic polyelectrolyte (polyamidoamine‐epichlorohydrin, PAE‐Cl) occurs in broader conditions when its original counter anion (Cl − ) is exchanged by bis(trifluoromethane‐sulphonyl)imide anion (TFSI − ), as a result of TFSI − counter anions association instead of polyelectrolyte complexation. This coacervate is catechol‐free, easy to prepare, and highlights robust wet adhesion strength on diverse submerged surfaces in salty water (pH = 3–11), as demonstrated by its versatile capability of in situ underwater gluing and repairing without any pre‐immersive drying. Abstract : A new polyelectrolyte coacervation phenomenon is observed, whose driven forces are the interactions between large‐sized counterions instead of polyelectrolyte complexation. The coacervate features high compatibility toward environmental pH and salt concentration. Thus, it highlights robust underwater adhesion in basic and salty conditions, in stark contrast to conventionalAbstract: Counterion exchange of charged macromolecules has comprehensive implications in biological and synthetic systems such as protein function, biosignaling, ion conducting, and separation, but the correlation between the dynamic ion exchange, polyelectrolyte phase separation, and functionality remains elusive. Here, counterion exchange is exploited as a means to facilitate liquid–liquid phase separation and coacervates featuring higher stability and versatility compared with conventional complex coacervate. Self‐coacervation of a cationic polyelectrolyte (polyamidoamine‐epichlorohydrin, PAE‐Cl) occurs in broader conditions when its original counter anion (Cl − ) is exchanged by bis(trifluoromethane‐sulphonyl)imide anion (TFSI − ), as a result of TFSI − counter anions association instead of polyelectrolyte complexation. This coacervate is catechol‐free, easy to prepare, and highlights robust wet adhesion strength on diverse submerged surfaces in salty water (pH = 3–11), as demonstrated by its versatile capability of in situ underwater gluing and repairing without any pre‐immersive drying. Abstract : A new polyelectrolyte coacervation phenomenon is observed, whose driven forces are the interactions between large‐sized counterions instead of polyelectrolyte complexation. The coacervate features high compatibility toward environmental pH and salt concentration. Thus, it highlights robust underwater adhesion in basic and salty conditions, in stark contrast to conventional complex coacervates that have been reported to fail under similar situations. … (more)
- Is Part Of:
- Macromolecular rapid communications. Volume 40:Issue 7(2019)
- Journal:
- Macromolecular rapid communications
- Issue:
- Volume 40:Issue 7(2019)
- Issue Display:
- Volume 40, Issue 7 (2019)
- Year:
- 2019
- Volume:
- 40
- Issue:
- 7
- Issue Sort Value:
- 2019-0040-0007-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2019-01-23
- Subjects:
- coacervates -- counterion exchange -- self‐assembly -- underwater adhesives
Macromolecules -- Periodicals
Polymers -- Periodicals
Chemistry -- Periodicals
547.705 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/marc.201800758 ↗
- Languages:
- English
- ISSNs:
- 1022-1336
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5330.400000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 9746.xml