Healable, Recyclable, and Programmable Shape Memory Organogels Based on Highly Malleable Catalyst-Free Carboxylate Linkages

被引:12
作者
Debnath, Suman [1 ]
Upadhyay, Chandan [1 ]
Ojha, Umaprasana [1 ]
机构
[1] Rajiv Gandhi Inst Petr Technol, Dept Chem, Jais 229304, India
关键词
covalent adaptable organogels; soft actuators; programmable shape memory ability; dynamic carboxylation; neighboring-group effects; NEIGHBORING GROUP PARTICIPATION; COVALENT POLYMER NETWORKS; MOLDABLE HYDROGELS; CREEP RESISTANCE; TRANSESTERIFICATION; HYDROLYSIS; SOLVENT; ESTERS; ACTUATION; BEHAVIOR;
D O I
10.1021/acsami.1c24946
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The development of healable and recyclable organogels possessing responsive abilities is mainly hindered by the unavailability of many dynamic covalent linkages that undergo exchange reaction below the boiling temperature of organic swelling medium. Furthermore, the exchange is desired to be effective under catalyst-free conditions to circumvent the issue of catalyst leaching during the swelling process. Especially, imparting swift reversibility to thermostable carboxylate linkages is challenging. In this approach, we have utilized the beta-keto anchimeric assistance as the tool to induce swift reversibility into the conventional carboxylate linkage under mild temperature (similar to 70-90 degrees C) and catalyst-free conditions. Using this beta-keto carboxylate linkage as an associative bond exchange mean, strong (tensile strength = 0.3 MPa) and stretchable (ultimate elongation approximate to 600%) covalent adaptable organogels (CAOs) with anisotropic swelling, remoldable, self-healing, and shape memory ability are derived from commercially available precursors. The shape memory ability of these samples shows dependency on the shape fixing time and can be programmed, targeting further applications. Soft actuators may be fabricated from the CAOs using temperature and solvent as the activating tools. This research demonstrates that the conventional carboxylate linkages can be made labile under mild conditions for further applications.
引用
收藏
页码:9618 / 9631
页数:14
相关论文
共 70 条
[1]   Chemically recyclable thermoplastics from reversible-deactivation polymerization of cyclic acetals [J].
Abel, Brooks A. ;
Snyder, Rachel L. ;
Coates, Geoffrey W. .
SCIENCE, 2021, 373 (6556) :783-+
[2]   Using Visible Light to Tune Boronic Acid-Ester Equilibria [J].
Accardo, Joseph, V ;
McClure, Emily R. ;
Mosquera, Martin A. ;
Kalow, Julia A. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2020, 142 (47) :19969-19979
[3]   Cold-set globular protein gels: Interactions, structure and rheology as a function of protein concentration [J].
Altlng, AC ;
Hamer, RJ ;
De Kruif, CG ;
Visschers, RW .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2003, 51 (10) :3150-3156
[4]   Recyclable Thermosets Based on Dynamic Amidation and Aza-Michael Addition Chemistry [J].
Baruah, Ranjana ;
Kumar, Anuj ;
Ujjwal, Rewati Raman ;
Kedia, Soumya ;
Ranjan, Amit ;
Ojha, Umaprasana .
MACROMOLECULES, 2016, 49 (20) :7814-7824
[5]   Metal-Catalyzed Transesterification for Healing and Assembling of Thermosets [J].
Capelot, Mathieu ;
Montarnal, Damien ;
Tournilhac, Francois ;
Leibler, Ludwik .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (18) :7664-7667
[6]   Dynamic Covalent Bonds in Polymeric Materials [J].
Chakma, Progyateg ;
Konkolewicz, Dominik .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2019, 58 (29) :9682-9695
[7]   THE NEIGHBORING GROUP PARTICIPATION BY THE CARBONYL GROUP IN THE HYDROLYSIS OF FLEXIBLE KETO-ESTERS AND ITS INHIBITION WHEN SUBSTRATES ARE PLACED INSIDE THE HELICAL CAVITIES OF AMYLOSE [J].
CHENG, XE ;
HUI, YZ ;
GU, JH ;
JIANG, XK .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1985, (02) :71-72
[8]   A new zinc hydroxide nitrate heterogeneous catalyst for the esterification of free fatty acids and the transesterification of vegetable oils [J].
Cordeiro, Claudiney Soares ;
Carbajal Arizaga, Gregorio Guadalupe ;
Ramos, Luiz Pereira ;
Wypych, Fernando .
CATALYSIS COMMUNICATIONS, 2008, 9 (11-12) :2140-2143
[9]   Malleable and Self-Healing Covalent Polymer Networks through Tunable Dynamic Boronic Ester Bonds [J].
Cromwell, Olivia R. ;
Chung, Jaeyoon ;
Guan, Zhibin .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (20) :6492-6495
[10]   Neighboring Group Participation and Internal Catalysis Effects on Exchangeable Covalent Bonds: Application to the Thriving Field of Vitrimer Chemistry [J].
Cuminet, Florian ;
Caillol, Sylvain ;
Dantras, Eric ;
Leclerc, Eric ;
Ladmiral, Vincent .
MACROMOLECULES, 2021, 54 (09) :3927-3961