Published Date
28 September 2016, Vol.101:415–449, doi:10.1016/j.polymer.2016.08.068
Author
Alexander V. Goponenko
Yuris A. Dzenis ,
28 September 2016, Vol.101:415–449, doi:10.1016/j.polymer.2016.08.068
Author
Department of Mechanical and Materials Engineering, Nebraska Center for Materials and Nanoscience, University of Nebraska-Lincoln, Lincoln, NE 68588-0526, USA
Received 23 March 2016. Revised 18 August 2016. Accepted 21 August 2016. Available online 24 August 2016.
Highlights
- Stimuli responsive gels are versatile, rapidly developing class of materials.
- •Mechanical aspects of gels are important but have not been sufficiently studied.
- •Low response rate and poor mechanical robustness remain critical issues for applications.
- •New ways to enhance gel response speed and robustness need to be developed.
- •Nanofilamentary materials that combine speed of nanogels with macroscopic size represent one possible solution.
Abstract
Due to their unique characteristics such as multifold change of volume in response to minute change in the environment, resemblance of soft biological tissues, ability to operate in wet environments, and chemical tailorability, stimuli-responsive gels represent a versatile and very promising class of materials for sensors, muscle-type actuators, biomedical applications, and autonomous intelligent structures. Success of these materials in practical applications largely depends on their ability to fulfill application-specific mechanical requirements. This article provides an overview of recent application-driven development of covalent polymer gels with special emphasis on the relevant mechanical factors and properties. A short account of mechanisms of gel swelling and mechanical characteristics of importance to stimuli-responsive gels is presented. The review highlights major barriers for wider application of these materials and discusses latest advances and potential future directions toward overcoming these barriers, including interpenetrating networks, homogeneous networks, nanocomposites, and nanofilamentary gels.
Graphical abstract
For further details log on website :
http://www.sciencedirect.com/science/article/pii/S0143749615002377
Keywords
- Hydrogels
- Stimuli-responsive gels
- Mechanical properties
- Swelling
- Sensors
- Actuators
Abbreviations
- 4VP
- 4-vinylpyridine
- AAc
- acrylic acid
- AAm
- acrylamide
- AFP
- α-fetoprotein (tumor-specific marker glycoprotein)
- AMERAH
- arm-wrestling match between an EAP actuated robotic arm and a human
- AMP
- adenosine 5′-monophosphate
- AMPS
- 2-acrylamido-2′-methylpropanesulfonic acid
- APTAC
- (3-acrylamidopropyl)trimethylammonium chloride
- ATP
- adenosine triphosphate
- BZ
- Belousov–Zhabotinsky (reaction)
- CMP
- cytidine 5′-monophosphate
- ConA
- concanavalin A
- DETA
- diethylene triamide
- DMAEM
- 2-dimethylamino ethyl methacrylate
- DMAPAAm
- N-(3-dimethylamino propyl) acrylamide
- EAP
- electroactive polymer
- GMP
- guanosine 5′-monophosphate
- GOx
- glucose oxidase
- HEMA
- 2-hydroxyethyl methacrylate
- iOA
- iso-octyl acrylate
- LCST
- low critical solution temperature
- MAAc
- methacrylic acid
- NEAAm
- N-ethylacrylamide
- NIPAM
- N-isopropylacrylamide
- P4VP
- poly(4-vinylpyridine)
- PAAc
- poly(acrylic acid)
- PAAm
- poly(acrylamide)
- PAMPS
- poly(2-Acrylamido-2-methylpropanesulfonic acid)
- PAN
- poly(acrylonitrile)
- PCCA
- polymerized colloidal crystalline arrays
- PDGI
- poly(dodecyl glyceryl itaconate)
- PEDOT
- poly(3,4-ethylenedioxythiophene)
- PEG
- poly(ethylene glycol)
- PMAAc
- poly(methacrylic acid)
- PMMA
- poly(methyl methacrylate)
- PNIPAM
- poly(N-isopropylacrylamide)
- PSS
- poly(styrenesulfonate)
- PVA
- poly(vinyl alcohol)
- QCM
- quartz crystal microbalance
- Ru(bpy)3
- ruthenium tris(2,2′-bipyridine)
- SRG
- stimuli-responsive gel
- TE
- tissue engineering
- TFMPA
- trifluoromethyl propenoic acid
- UCST
- upper critical solution temperature
- UMP
- uridine 5′-monophosphate
- VI
- vinyl imidazole
- α-CD
- α-cyclodextrin
Vitae
Alexander Goponenko received his M.S. in Materials Science from Lomonosov Moscow State University (1997) and Ph.D. in Macromolecular Chemistry from Karpov Institute of Physical Chemistry (2000). After working as a postdoc at University of Pittsburgh (2001–2004) and at University of Nebraska Medical Center (2005–2006), he has been employed as a Research Assistant Professor in the Department of Mechanical and Materials Engineering at University of Nebraska–Lincoln. His research interests include polymer gels and nanostructured materials.
Yuris Dzenis is a McBroom Professor of Engineering at UNL. He has earned his PhD in Aerospace and Mechanical Engineering from the University of Texas-Arlington, PhD in Physics and Mechanics of Polymers from Latvian Academy of Sciences, and MS in Physics (Electrodynamics of Continua) from Latvian University. His research interests are in design, manufacturing, modeling, and characterization of advanced nanomaterials and composites. He has introduced and developed several nanomanufacturing and hybrid manufacturing technologies to produce advanced nanomaterials. He has pioneered development of cost-effective delamination resistant structural composites with nanoreinforced interfaces. Most recent advances include the discovery and explanation of simultaneously high strength and toughness of ultrafine continuous polymer nanofibers.
- ∗ Corresponding author.
For further details log on website :
http://www.sciencedirect.com/science/article/pii/S0143749615002377
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