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Advances in Smart Polymers and Polymeric Nanocomposites

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Materials Chemistry".

Deadline for manuscript submissions: closed (15 August 2022) | Viewed by 30269

Special Issue Editors


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Guest Editor
Institute of Polymer Science and Technology (ICTP), CSIC, C/Juan de la Cierva, 3, 28006 Madrid, Spain
Interests: materials science; nanomaterials; polymer science; composites and nanocomposites; smart materials and stimuli-responsive polymers; shape memory and multi-responsive polymers; multifunctional polymers; biodegradable and biobased polymers; 3D printing; reuse and recycling
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Assistant Guest Editor
University of Alcalá, Madrid, Spain
Interests: biopolymers; catalysis; biocompatible materials; materials for electric engineering and electronics, smart materials, stimuli-responsive materials, shape memory and multifunctional polymers, piezoelectric biopolymers, piezoelectric harvesters, biodegradable, biobased and natural polymers, green nanocomposites, green chemestry, ecofriendly and soustainable polymer synthesis and processing methods
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

In recent years, many interesting studies on smart materials have been developed. Scientists are strongly inspired by nature to design smart materials that use biomimicry to emulate the behavior of living organisms and, by taking advantage of the ability of the material to interact with its surrounding, to provide an adaptive response to environmental changes. Among them, stimuli-responsive materials are attractive materials for a wide range of innovative applications in both technical industries (i.e., aeronautics, electronics, textile, and packaging) and the biomedical field (i.e., stents, scaffold, etc.), indicating their multidisciplinary character in materials science, chemistry, and engineering.

Smart polymers can be classified into the following three groups according to the stimuli they respond to: Physical—temperature, ultrasounds, light, electric or magnetic field or mechanical stress, etc.; Chemical—pH, ligands, and ionic strength, etc.; Biological—enzymes and biomolecules.

It is important to highlight that such responsiveness is not an intrinsic property of the material. It is obtained by properly designing the meso- or macroscopic arrangement of the constitutive elements or by the chemistry underlying the microstructure of the material. In particular, when the responsiveness at the molecular level is properly organized, the nanoscale response can be collectively detected at the macroscale, leading to a responsive material.

Different strategies have been used for the design of smart materials that can be triggered by several stimuli depending on the final applications. The responsiveness can be achieved by the introduction of either chemical or non-covalent bonds (i.e., photodimerization of coumarin, Diels–Alder reactions, supramolecular interactions, and dipolar interaction) or physical interactions, i.e., crystallites, glassy hard domains, hydrogen bonding, ionic clusters, chain entanglements, and interpenetrating networks. Additionally, smart polymers can be designed as “multimaterial” systems, such as multiblock copolymer and covalent polymer networks, as well as the preparation of blends from two or more polymers by a physical process. Despite their unique properties, the potential applications of smart polymers are often limited due to their low thermal conductivity, inertness to electrical stimulus, slow responsiveness to light and electromagnetic stimuli, and low recovery time during actuation. To overcome these difficulties, a new generation of smart polymeric nanocomposites can be designed. Generally, they are produced by the incorporation of one or more nanofillers, such as nanotubes, nanofibers, nanocrystals, etc., within the polymer matrix in order to increase their matrix properties, as well as to give them multifunctionality. However, it is important to point out that when a polymer presents a responsiveness to a trigger, it is not so trivial that its corresponding nanocomposites continue to show the same response at the same conditions. Therefore, many efforts are needed in this sense to obtain advanced smart polymeric nanocomposites.

This Special Issue in “Advances in Smart Polymers and Polymeric Nanocomposites” will bring together the more recent scientific achievements in the field of smart polymers and nanocomposites, focusing on the different strategies to design high-performance and multi-responsive materials.

Dr. Laura Peponi
Dr. Valentina Sessini
Guest Editor

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Keywords

  • smart materials
  • stimuli-responsive materials
  • shape memory properties
  • shape memory nanocomposites
  • multi-responsive polymers
  • multifunctional polymers
  • piezoelectric polymers and composites
  • self-healing polymers and composites

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Published Papers (4 papers)

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Research

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20 pages, 6764 KiB  
Article
Actuating Shape Memory Polymer for Thermoresponsive Soft Robotic Gripper and Programmable Materials
by Dennis Schönfeld, Dilip Chalissery, Franziska Wenz, Marius Specht, Chris Eberl and Thorsten Pretsch
Molecules 2021, 26(3), 522; https://doi.org/10.3390/molecules26030522 - 20 Jan 2021
Cited by 45 | Viewed by 7452
Abstract
For soft robotics and programmable metamaterials, novel approaches are required enabling the design of highly integrated thermoresponsive actuating systems. In the concept presented here, the necessary functional component was obtained by polymer syntheses. First, poly(1,10-decylene adipate) diol (PDA) with a number average molecular [...] Read more.
For soft robotics and programmable metamaterials, novel approaches are required enabling the design of highly integrated thermoresponsive actuating systems. In the concept presented here, the necessary functional component was obtained by polymer syntheses. First, poly(1,10-decylene adipate) diol (PDA) with a number average molecular weight Mn of 3290 g·mol−1 was synthesized from 1,10-decanediol and adipic acid. Afterward, the PDA was brought to reaction with 4,4′-diphenylmethane diisocyanate and 1,4-butanediol. The resulting polyester urethane (PEU) was processed to the filament, and samples were additively manufactured by fused-filament fabrication. After thermomechanical treatment, the PEU reliably actuated under stress-free conditions by expanding on cooling and shrinking on heating with a maximum thermoreversible strain of 16.1%. Actuation stabilized at 12.2%, as verified in a measurement comprising 100 heating-cooling cycles. By adding an actuator element to a gripper system, a hen’s egg could be picked up, safely transported and deposited. Finally, one actuator element each was built into two types of unit cells for programmable materials, thus enabling the design of temperature-dependent behavior. The approaches are expected to open up new opportunities, e.g., in the fields of soft robotics and shape morphing. Full article
(This article belongs to the Special Issue Advances in Smart Polymers and Polymeric Nanocomposites)
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16 pages, 5111 KiB  
Article
Reprogrammable Permanent Shape Memory Materials Based on Reversibly Crosslinked Epoxy/PCL Blends
by Iker Razquin, Alvaro Iregui, Lidia Orduna, Loli Martin, Alba González and Lourdes Irusta
Molecules 2020, 25(7), 1568; https://doi.org/10.3390/molecules25071568 - 29 Mar 2020
Cited by 8 | Viewed by 2924
Abstract
Epoxy/Polycaprolactone (PCL) blends cured with a conventional diamine (4,4′-diaminodiphenylmethane, DDM) and with different amounts of a disulfide containing diamine (4, 4´-dithioaniline, DSS) were prepared through melting. The curing process was studied by FTIR and differential scanning calorimetry (DSC) and the mechanical behavior of [...] Read more.
Epoxy/Polycaprolactone (PCL) blends cured with a conventional diamine (4,4′-diaminodiphenylmethane, DDM) and with different amounts of a disulfide containing diamine (4, 4´-dithioaniline, DSS) were prepared through melting. The curing process was studied by FTIR and differential scanning calorimetry (DSC) and the mechanical behavior of the networks was studied by DMA. The shape memory properties and the recyclability of the materials were also analyzed. All blends showed a very high curing degree and temperature activated shape memory effect, related to the glass transition of the epoxy resin. The PCL plasticized the mixture, allowing tailoring of the epoxy glass transition. In addition, in the blends cured with DSS, as a consequence of the disulfide exchange reaction, the permanent shape could be erased and a new shape could be reprogrammed. Using this strategy, reprogrammable permanent shape memory materials were obtained. Full article
(This article belongs to the Special Issue Advances in Smart Polymers and Polymeric Nanocomposites)
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Review

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27 pages, 11036 KiB  
Review
Shape-Memory Polymeric Artificial Muscles: Mechanisms, Applications and Challenges
by Yujie Chen, Chi Chen, Hafeez Ur Rehman, Xu Zheng, Hua Li, Hezhou Liu and Mikael S. Hedenqvist
Molecules 2020, 25(18), 4246; https://doi.org/10.3390/molecules25184246 - 16 Sep 2020
Cited by 56 | Viewed by 7979
Abstract
Shape-memory materials are smart materials that can remember an original shape and return to their unique state from a deformed secondary shape in the presence of an appropriate stimulus. This property allows these materials to be used as shape-memory artificial muscles, which form [...] Read more.
Shape-memory materials are smart materials that can remember an original shape and return to their unique state from a deformed secondary shape in the presence of an appropriate stimulus. This property allows these materials to be used as shape-memory artificial muscles, which form a subclass of artificial muscles. The shape-memory artificial muscles are fabricated from shape-memory polymers (SMPs) by twist insertion, shape fixation via Tm or Tg, or by liquid crystal elastomers (LCEs). The prepared SMP artificial muscles can be used in a wide range of applications, from biomimetic and soft robotics to actuators, because they can be operated without sophisticated linkage design and can achieve complex final shapes. Recently, significant achievements have been made in fabrication, modelling, and manipulation of SMP-based artificial muscles. This paper presents a review of the recent progress in shape-memory polymer-based artificial muscles. Here we focus on the mechanisms of SMPs, applications of SMPs as artificial muscles, and the challenges they face concerning actuation. While shape-memory behavior has been demonstrated in several stimulated environments, our focus is on thermal-, photo-, and electrical-actuated SMP artificial muscles. Full article
(This article belongs to the Special Issue Advances in Smart Polymers and Polymeric Nanocomposites)
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13 pages, 3224 KiB  
Review
A Review on Liquid Crystal Polymers in Free-Standing Reversible Shape Memory Materials
by Zhibin Wen, Keke Yang and Jean-Marie Raquez
Molecules 2020, 25(5), 1241; https://doi.org/10.3390/molecules25051241 - 10 Mar 2020
Cited by 42 | Viewed by 10548
Abstract
Liquid crystal polymers have attracted massive attention as stimuli-responsive shape memory materials due to their unique reversible large-scale and high-speed actuations. These materials can be utilized to fabricate artificial muscles, sensors, and actuators driven by thermal order–disorder phase transition or transcis [...] Read more.
Liquid crystal polymers have attracted massive attention as stimuli-responsive shape memory materials due to their unique reversible large-scale and high-speed actuations. These materials can be utilized to fabricate artificial muscles, sensors, and actuators driven by thermal order–disorder phase transition or transcis photoisomerization. This review collects most commonly used liquid crystal monomers and techniques to macroscopically order and align liquid crystal materials (monodomain), highlighting the unique materials on the thermal and photo responsive reversible shape memory effects. Challenges and potential future applications are also discussed. Full article
(This article belongs to the Special Issue Advances in Smart Polymers and Polymeric Nanocomposites)
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