Quick water-responsive shape memory hybrids with cellulose nanofibers

A type of quick water-responsive shape memory hybrids is fabricated by introducing cellulose nanofibrous mats as the filler in a polymeric matrix. Cellulose nanofibrous mats are obtained through hydrolyzing electrospun cellulose acetate (CA) nanofibers, then casted in thermoplastic polyurethane (TPU) solution to form the hybrids. The quick shape memory behavior of the formed hybrids is demonstrated using dynamic mechanical analysis (DMA) and stress–strain cyclic test. According to a predetermined protocol, the hybrids present desirable shape fixation and recovery, and the elastic modulus (E′) is shown to be responsive promptly and reversibly against drying and wetting cycle. Shape memory mechanism of the hybrids involves the reversible and competitive hydrogen bonds within cellulose before and after water immersion as well as the entropy elasticity of the TPU matrix. This study can pave a way to design novel smart materials by facile methods through incorporating natural nanomaterials as water sensitive fillers. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 767–775     

Bio‐based hyperbranched polyurethane/Fe3O4 nanocomposites as shape memory materials

The bio‐based shape memory polymers have generated immense interest as advanced smart materials. Mesua ferrea L. seed oil‐based hyperbranched polyurethane (HBPU)/Fe₃O₄ nanocomposites were prepared by the in‐situ polymerization technique. The transmission electron microscopy confirmed the homogeneous distribution of the Fe₃O₄ nanoparticles in polymer matrix, whereas Fourier transform infrared spectroscopic study revealed the presence of strong interfacial interactions between them. The incorporation of Fe₃O₄ (0 to 10 wt%) into the HBPU resulted in an increase in tensile strength (5.5–15 MPa) and scratch resistance (3–6 kg). The thermo‐gravimetric analysis indicated the improvement of thermal stability (240–270°C) of the nanocomposites. The nanocomposites exhibited full shape fixity, as well as almost full shape recovery under the microwave stimulus. The shape recovery speed increased with the increase of Fe₃O₄ nanoparticles content in the nanocomposites. Thus, the studied nanocomposites might be used as advanced shape memory materials in different potential fields. Copyright © 2013 John Wiley & Sons, Ltd.     

Shape‐memory effect in hyperbranched poly(ethyleneimine)‐modified epoxy thermosets

A series of shape‐memory epoxy thermosets were synthesized by crosslinking diglycidyl ether of bisphenol A with mixtures of commercially available hyperbranched poly(ethyleneimine) and polyetheramine. Thermal, mechanical and shape‐memory properties were studied and the effect on them of the content and structure of the hyperbranched polymer was discussed. Measurements showed that the glass transition temperature can be tailored from 60 °C to 117 °C depending on the hyperbranched polymer content, and all formulations showed an appropriate glassy/rubbery storage modulus ratio. Shape‐memory programming was carried out at TgE′ given the excellent mechanical properties of the materials, with maximum stress and failure strain up to 15 MPa and 60%, respectively. The resulting shape‐memory behavior was excellent, with maximum shape recovery and shape fixity of 98% as well as a fast shape‐recovery rate of 22%/min. The results show that hyperbranched poly(ethyleneimine) as a crosslinking agent can be used to enhance mechanical and shape‐memory properties with different effects depending on the crosslinking density. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015 , 53, 924–933     

Synthesis and shape memory behavior study of hyperbranched poly(urethane-tetrazole)

A novel hyperbranched poly(urethane-tetrazole)(HPUTZ) was synthesized via the A2+BB2' approach using hexadiisocyanate(HDI) and 3-(bis-(2-hydroxyethyl)) aminopropyltetrazole(HAPTZ).The molecular structure was characterized by FTIR and 1H NMR spectroscopy.The number average molecular weight was measured to be 1.05×104 g/mol with a polydispersity of 1.27 by GPC analysis.The HPUTZ was further cured by the semi-adduct(PEG-IPDI) from polyethylene glycol(PEG) reacting with isophorone diisocyanate(IPDI) to form th...     

Recovery stress and work output in hyperbranched poly(ethyleneimine)‐modified shape‐memory epoxy polymers

In this study a series of hyperbranched modified shape‐memory polymers were subjected to constrained shape recoveries in order to determine their potential use as thermomechanical actuators. Materials were synthesized from a diglycidyl ether of bisphenol A as base epoxy and a polyetheramine and a commercial hyperbranched poly(ethyleneimine) as crosslinker agents. Hyperbranched polymers within the structure of the shape‐memory epoxy polymers led to a more heterogeneous network that can substantially modify mechanical properties. Thermomechanical and mechanical properties were analyzed and discussed in terms of the content of hyperbranched polymer. Shape‐memory effect was analyzed under fully and partially constrained conditions. When shape recovery was carried out with fixed strain a recovery stress was obtained whereas when it was carried out with a constraining stress the material performs mechanical work. Tensile tests at Tg^E′ showed excellent values of stress and strain at break (up to 15 MPa and almost 60%, respectively). Constrained recovery performances revealed rapid recovery stress generation and unusually high recovery stresses (up to 7 MPa) and extremely high work densities (up to 750 kJ/m³). The network structure of shape‐memory polymers was found to be a key factor for actuator‐like applications. Results confirm that hyperbranched modified‐epoxy shape memory polymers are good candidates for actuator‐like shape‐memory applications. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 1002–1013     

Organic‐montmorillonite modified shape memory epoxy composite

A series of organic‐montmorillonite (OMMT) modified shape memory epoxy (SMEP) composites were prepared for the purpose of application on space deployable structures. Tensile test, dynamic mechanical analysis (DMA), X‐ray diffraction (XRD), scanning electron microscope (SEM), and fold‐deploy shape memory test methods were used to characterize the mechanical, structure, and shape memory properties of these materials. The results showed addition of OMMT could improve the composites' toughness, tensile strength, transition temperature, and shape recovery speed, while shape recovery ratio was unaffected. Composite with 3wt%. OMMT had the optimum combination property. It could fully recover its original shape in about 2 min at 185°C under the maximum bending angle of 180°. Its elongation at break and tensile strength were increased by 835 and 17.4%, respectively, compared to that of neat SMEP. The transition temperature also slightly increased. Copyright © 2010 John Wiley & Sons, Ltd.     

Thermal,mechanical and electroactive shape memory properties of polyurethane (PU)/poly (lactic acid) (PLA)/CNT nanocomposites

Polymer blend nanocomposites based on thermoplastic polyurethane (PU) elastomer, polylactide (PLA) and surface modified carbon nanotubes were prepared via simple melt mixing process and investigated for its mechanical, dynamic mechanical and electroactive shape memory properties. Chemical and structural characterization of the polymer blend nanocomposites were investigated by Fourier Transform infrared (FT-IR) and wide angle X-ray diffraction (WAXD). Loading of the surface modified carbon nanotube in the PU/PLA polymer blends resulted in the significant improvement on the mechanical properties such as tensile strength, when compared to the pure and pristine CNT loaded polymer blends. Dynamic mechanical analysis showed that the glass transition temperature (T_g) of the PU/PLA blend slightly increases on loading of pristine CNT and this effect is more pronounced on loading surface modified CNTs. Thermal and electrical properties of the polymer blend composites increases significantly on loading pristine or surface modified CNTs. Finally, shape memory studies of the PU/PLA/modified CNT composites exhibit a remarkable recoverability of its shape at lower applied dc voltages, when compared to pure or pristine CNT loaded system.     

Effect of methoxy position on dynamic mechanical and shape memory properties of methoxyphenol-based polybenzoxazines

Abstract

Two series of benzoxazines were synthesized from o-, m-, and p-methoxyphenols, two polyetheramines with different molecular weights, and formaldehyde. The glass transition temperatures (T _gs) of m-methoxyphenol-based polybenzoxazines are respectively higher than those of o- and p-methoxyphenol-based counterparts. The polybenzoxazines exhibit thermally induced one-way dual-shape memory behavior based on T _g, and the o- and p-methoxyphenol-based polybenzoxazines exhibit higher shape memory performance than m-methoxyphenol-based counterparts under motion constraints.     

Mechanical and shape‐memory properties of poly(mannitol sebacate)/cellulose nanocrystal nanocomposites

Polyesters based on polyols and sebacic acid, known as poly(polyol sebacate)s (PPS), are attracting considerable attention, as their properties are potentially useful in the context of soft‐tissue engineering applications. To overcome the drawback that PPSs generally display rather low strength and stiffness, we have pursued the preparation of nanocomposites based poly(mannitol sebacate) (PMS), a prominent example of this materials family, with cellulose nanocrystals (CNCs). Nanocomposites were achieved in a two‐step process. A soluble, low‐molecular‐weight PMS pre‐polymer was formed via the polycondensation reaction between sebacic acid and D‐mannitol. Nanocomposites with different CNC content were prepared by solution‐casting and curing under vacuum using two different profiles designed to prepare materials with low and high degree of crosslinking. The as‐prepared nanocomposites have higher stiffness and toughness than the neat PMS matrix while maintaining a high elongation at break. A highly crosslinked nanocomposite with a CNC content of 5 wt % displays a sixfold increase in Young's modulus and a fivefold improvement in toughness. Nanocomposites also exhibit a shape memory effect with a switch temperature in the range of 15 to 45 °C; in particular the materials with a thermal transition in the upper part of this range are potentially useful for biomedical applications. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 3123–3133     

Fabrication of well‐defined shape memory graft polymers derived from biomass: An insight into the effect of side chain architecture on shape memory properties

Fully sustainable shape memory polymers (SMPs) derived from ethyl cellulose (EC, derived from cellulose), tetrahydrofurfuryl methacrylate (THFMA, derived from furfural), and lauryl methacrylate (LMA, derived from fatty acids) were prepared via “grafting from” atom transfer radical polymer (ATRP). The “grafting from” ATRP strategy allows to fabricate SMPs with EC as a backbone, and LMA and THFMA copolymer as a side chain. By utilizing the one‐pot and sequential monomer addition approach, two types of SMPs with random/semi‐block side chain architectures were obtained, respectively. Random/semi‐block side chain architecture of SMPs was confirmed by DSC, DMA, SAXS, and TEM. The presence of microphase separation in the SMPs with semi‐block side chain architecture provided two distinct thermal transitions, which was needed for triple‐shape memory behavior. Shape memory study showed that SMPs with semi‐block side chain architecture exhibited excellent triple‐shape memory property, and also had higher shape recovery speed and shape recovery ratio than those with random side chain architecture. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56, 1711–1720     

Synthesis and memory characteristics of highly organo‐soluble hyperbranched polyimides with various electron acceptors

A series of hyperbranched polyimides (HBPIs) were synthesized by reacting a triamine monomer N ,N ′,N ″‐tris(4‐methoxyphenyl)‐N ,N ′,N ″‐tris(4‐phenylamino)?1,3,5‐benzenetriamine with various dianhydrides such as oxydiphthalic dianhydride (ODPA), 3,3′,4,4′‐diphenylsulfonetetracarboxylic dianhydride (DSDA), 3,3′,4,4′‐benzophenonetetracarboxylic dianhydride (BTDA), and pyromellitic dianhydride (PMDA). The hyperbranched polyimide (6FHBPI) using 4,4′‐(hexafluoroisopropylidene)diphthalic anhydride (6FDA) as dianhydride monomer was also added into the discussion. All the hyperbranched polyimides exhibited excellent organo‐solubility and high thermal stability. Memory devices with a sandwiched structure of indium tin oxide (ITO)/HBPI/Al were constructed by using these HBPIs as the active layers. All these HBPIs based memory devices exhibited favorable memory performances, with switching voltages between ?1.3 V and ?2.5 V, ON/OFF current ratios up to 10⁷ and retention times long to 10⁴ s. Tunable memory characteristics from electrical insulator to volatile memory, and then to nonvolatile memory were obtained by adjusting the electron acceptors of these HBPIs. Molecular simulation results suggested that the electron affinity and the dipole moment of these HBPIs were responsible for the conversion of the memory characteristics. With the electron affinity and dipole moment of these HBPIs increasing, the memory characteristics turned from volatile to nonvolatile. The present study suggested that tunable memory performance could be achieved through adjusting the acceptor moieties of the hyperbranched polyimides. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55 , 2281–2288     

Actuation design for high‐performance shape memory polyurethanes

A series of shape memory polyurethanes were synthesized from poly(tetramethylene glycol), 4,4‐methylene diphenyl diisocyanate, and 1,3‐butanediol. The prepolymers with different molecular weights (M_c) were capped with 2‐hydroxyl ethylacrylate or 3‐aminopropyltriethoxysilane (APTES) and crosslinked by UV curing or a sol–gel reaction. Variations of the crosslinker functionality (f), subchain density (N), and hard segment content (HSC) produced systematic variations of the glass transition temperature (6–45 °C), accompanied by changes in the mechanical, dynamic mechanical and shape memory properties. More than 95% of shape fixity and 98% of shape recovery up to the fourth cycles were obtained with APTES crosslinked 3000M_c with 30% of HSC. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2013 , 51, 1473–1479     

Hydrogel‐coated polyurethane/urea shape memory polymer foams

Shape memory polymers (SMPs) are a class of responsive polymers that have attracted attention in designing biomedical devices because of their potential to improve minimally invasive surgeries. Use of porous SMPs in vascular grafts has been proposed because porosity aids in transfer of fluids through the graft and growth of vascular tissue. However, porosity also allows blood to leak through grafts so preclotting the materials is necessary. Here hydrogels have been synthesized from acrylic acid and N‐hydroxyethyl acrylamide and coated around a porous SMP produced from lactose functionalized polyurea‐urethanes. The biocompatibility of the polymers used to prepare the cross‐linked shape memory material is demonstrated using an in vitro cell assay. As expected, the hydrogel coating enhanced fluid uptake abilities without hindering the shape memory properties. These results indicate that hydrogels can be used in porous SMP materials without inhibiting the shape recovery of the material. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 1389–1395     

Structure–property relationships of fatty acid swollen,crosslinked natural rubber shape memory polymers

This article investigates shape memory polymers (SMPs) fabricated by swelling sulfur crosslinked natural rubber with four different molten fatty acids: lauric, myristic, palmitic, and stearic acid. As inexpensive additives, they allow commodity natural rubber to be directly converted to SMPs. The shape memory properties are investigated as a function of wt% fatty acid, the choice of fatty acid, and the applied load during shape memory programming. It is found that increasing the wt% acid improves the shape fixity up to ca. 97% at ≥50 wt% fatty acid, at which point the recovery starts to decline with increasing wt% acid due to network failure during shape programming. The shape fixity is found to depend on the yield stress and modulus of the fatty acid network, which both increase with increasing wt% acid. The choice of fatty acid also varies the trigger temperature for shape memory, which scales with the melting point of the fatty acid. Serendipitously, it is found that alignment of the fatty acid crystals during programming produces stiffer networks whose modulus increase with applied load, which counterbalances the higher elastic energy stored in the rubber network to produce lower sensitivity of the shape fixity to the applied load. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018 , 56, 673–687     

Effect of comonomer on thermal/mechanical and shape memory property of L‐lactide‐based shape‐memory copolymers

In this study, three kinds of L ‐lactide‐based copolymers, poly(lactide‐co‐glycolide) (PLGA), poly(lactide‐co‐p‐dioxanone) (PLDON) and poly(lactide‐co‐caprolactone) (PLC), were synthesized by the copolymerization of L ‐lactide (L) with glycolide (G), or p‐dioxanone (DON) or ε‐caprolactone (CL), respectively. The copolymers were easily soluble in common organic solvents. The compositions of the copolymers were determined by ¹H‐NMR. Thermal/mechanical and shape‐memory properties of the copolymers with different comonomers were compared. Moreover, the effect of the chain flexibility of the comonomers on thermal/mechanical and shape‐memory properties of the copolymers were investigated. The copolymers with appropriate lactyl content showed good shape‐memory properties where both the shape fixity rate (R_f)and the shape recovery rate (R_r) could exceed 95%. It was found that the comonomers with different flexible molecular chain have different effects on their thermal/mechanical and shape‐memory properties. Among them, PLGA has the highest mechanical strength and recovery rate while PLC copolymer has high recovery rate when the lactyl content exceeded 85% and the lowest transition temperature (T_trans). Copyright © 2007 John Wiley & Sons, Ltd.     

Shape memory polymers with interconnected nanopores and high mechanical strength

The fabrication of shape memory polymers with both interconnected nanopores and high mechanical strength is challenging. In this work, porous shape memory polymers (PSMPs) were prepared based on the combination of crystallization and phase separation in a ternary blend of poly(l ‐lactic acid)/polyvinyl acetate/poly(ethylene oxide) (i.e., PLLA/PVAc/PEO). The phase separation between the PLLA and PVAc/PEO resulted in bicontinuous structures in microscale including a PLLA‐rich phase and a mixed PVAc/PEO phase. On one hand, the continuous PLLA‐rich phase contributed to the high mechanical strength and shape memory performance, in which tiny crystals and amorphous matrix of PLLA act as the shape fixed phase and reversible phase, respectively. On the other hand, the crystallization of PEO in the miscible PVAc/PEO blend produced submicrometer bicontinuous structures. The interconnected nanopores have been obtained by selective etching of the PEO. Our strategy opens a new avenue for fabricating PSMPs with both interpenetrated channels and high strength. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018 , 56, 125–130     

Organic–inorganic polyurethanes with double decker silsesquioxanes in the main chains: Morphologies,surface hydrophobicity,and shape memory properties

In this contribution, we reported an investigation of the morphologies, surface hydrophobicity, and shape memory properties of the organic–inorganic polyurethanes with double decker silsesquioxane (DDSQ) in the main chains. It was found that the organic–inorganic polyurethanes were microphase‐separated and that the POSS cages in the main chains were self‐organized into the spherical microdomains with the size of 10–50 nm in diameter. The introduction of POSS cages into the main chains resulted in the enhancement of glass transition temperatures (T_g's). In the meantime, the surface dewettability of the materials was significantly enhanced. X‐ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM) indicates the improvement of the surface hydrophobicity resulted from the enrichment of POSS at the surfaces of the polyurethanes. The mechanical analyses, such as dynamic mechanical analysis (DMA) and creep‐recovery analysis (CRA), indicate that the POSS microdomains dispersed in the polyurethanes behaved as the physical crosslinking sites and promoted the formation of the crosslinked networks. Owing to the introduction of DDSQ into the main chains, the organic–inorganic polyurethanes significantly displayed shape memory properties, in marked contrast to the unmodified and linear polyurethane. The shape memory behavior has been addressed on the formation of the strong physically crosslinked networks in the organic–inorganic polyurethanes. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018 , 56, 893–906     

Improved mechanical properties of epoxy‐based composites with hyperbranched polymer grafting glass‐fiber

A glass‐fiber, grafted by hyperbranched polymer with hydroxyl group (GF‐HBPH), reinforced epoxy‐based composite was evaluated for mechanical properties and compared with the neat epoxy and silanized glass‐fiber, GF‐APS. The epoxy/GF‐HBPH composites were studied by attenuated total internal reflectance infrared spectroscopy, ¹H nuclear magnetic resonance spectroscopy, thermal gravimetric analysis, mechanical properties analysis, and field emission‐scanning electron microscopy. The results showed that the incorporation of GF‐HBPH could simultaneously enhance the mechanical properties of the epoxy composites. Field emission‐scanning electron microscopy images of the fracture surfaces of the test specimens were used to support the results and conclusions. Copyright © 2016 John Wiley & Sons, Ltd.     

Shape memory properties of dynamically vulcanized poly(lactic acid)/nitrile butadiene rubber (PLA/NBR) thermoplastic vulcanizates: The effect of ACN content in NBR

Morphology structure and interfacial interaction are crucial factors for shape memory thermoplastic vulcanizates. In this study, shape memory thermoplastic vulcanizates based on poly(lactic acid) (PLA) and nitrile butadiene rubber (NBR) were prepared through dynamic vulcanization. The influence of acrylonitrile (ACN) content on the morphology, compatibility, shape memory property, and mechanical property was investigated. A co‐continuous structure was observed. The interfacial compatibilization between PLA and NBR phases occurred, resulting in a significantly improved interface adhesion and interfacial interaction, which was confirmed by Fourier transform infrared spectroscopy. With such a novel structure, the PLA/NBR TPVs owned an excellent shape memory property and further improved with increasing ACN content of NBR, which could be explained that the cross‐linked continuous NBR phase provided a stronger recovery driving force. In the meantime, tensile strength and elongation at break of TPVs increased with increase in ACN content. It is concluded that the preparation of dynamically vulcanized thermoplastic vulcanizate with co‐continuous structure and strong interfacial adhesion is beneficial to obtain outstanding shape memory effect.     

Connecting free volume with shape memory properties in noncytotoxic gamma‐irradiated polycyclooctene

The free volume holes of a shape memory polymer have been analyzed considering that the empty space between molecules is necessary for the molecular motion, and the shape memory response is based on polymer segments acting as molecular switches through variable flexibility with temperature or other stimuli. Therefore, thermomechanical analysis (TMA) and positron annihilation lifetime spectroscopy (PALS) have been applied to analyze shape recovery and free volume hole sizes in gamma‐irradiated polycyclooctene (PCO) samples, as a noncytotoxic alternative to more conventional PCO crosslinked via peroxide for future applications in medicine. Thus, a first approach relating structure, free volume holes and shape memory properties in gamma‐irradiated PCO is presented. The results suggest that free volume holes caused by gamma irradiation in PCO samples facilitate the recovery process by improving movement of polymer chains and open possibilities for the design and control of the macroscopic response. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015 , 53, 1080–1088