Abstract:source. Ko et al. construct a temperature-responsive SMP film by integrating polylactic acid (PLA) and thermoplastic polyurethane (TPU). [15] Ni et al. simply adjust the layers of graphene oxide coating on SMP to design thermal-responsive devices. [16] However, the single responsive ability cannot meet the requirement of increasingly complex and changeable application environment. [17][18][19] On the other hand, the solid planar or strip geometries of traditional SMPs limit the expansion of new horizons. [20][… Show more
“…Once a cross-linked network is formed, its permanent shape cannot be changed. However, for vitrimer containing dynamic ester bonds, thermally induced dynamic transesterification imparts configurable memory properties to the material, offering possibilities for reshaping the curing material. , As shown in Figure c, when compressed from its original diameter of 34 to 15 mm, it was observed that the EPC foam could be perfectly restored to its initial state of 34 mm after heating at 120 °C and removal of external force, indicating its exceptional shape memory properties. , Additionally, in Figure d, a rectangular-shaped foam could be temporarily reshaped into an “n” shape by heating it to 120 °C (above T g ). After cooling to room temperature, the foam maintained its temporary “n” shape.…”
Section: Resultsmentioning
confidence: 97%
“…53,54 As shown in Figure 5c, when compressed from its original diameter of 34 to 15 mm, it was observed that the EPC foam could be perfectly restored to its initial state of 34 mm after heating at 120 °C and removal of external force, indicating its exceptional shape memory properties. 55,56 Additionally, in Figure 5d, a rectangular-shaped foam could be temporarily reshaped into an "n" shape by heating it to 120 °C (above T g ). After cooling to room temperature, the foam maintained its temporary "n" shape.…”
Section: Mechanical and Thermal Properties Of Epc-xmentioning
Thermosetting foams have limited capabilities for recycling, reprocessing, or reshaping. Moreover, most of the foaming agents currently employed in these foams are derived from organic compounds sourced from petrochemicals, thereby posing a significant environmental threat due to heightened pollution. To solve these problems, a fully biobased degradable vitrimer foam (EPC-X) was fabricated using an environmentally friendly all-in-one foaming strategy by cross-linking epoxidized malepimaric anhydride (EMPA), 1,5diaminopentane (PDA), and 1,5-diaminopentane carbamate (PDAC) as a latent curing-blowing agent. To our delight, the vitrimer foams exhibit excellent mechanical properties (2.86 ± 0.11 MPa compressive strength) owing to their unique rigid rosin backbone and cross-linking networks. The presence of dynamic β-hydroxy ester bonds and the selfcatalytic behavior of tertiary amine groups facilitate network rearrangement without requiring additional catalysts, thereby resulting in the development of EPC-X with rapid self-healing and shape memory properties. The self-healing foam could support a weight of 500 g (approximately 562 times its own mass). Moreover, these high-performance vitrimer foams can also be easily degraded in an ethanolamine (EA) or NaOH solution under mild conditions. Such a design strategy offers an alternative approach for developing superior degradable and thermal stimuli-responsive thermosetting foams.
“…Once a cross-linked network is formed, its permanent shape cannot be changed. However, for vitrimer containing dynamic ester bonds, thermally induced dynamic transesterification imparts configurable memory properties to the material, offering possibilities for reshaping the curing material. , As shown in Figure c, when compressed from its original diameter of 34 to 15 mm, it was observed that the EPC foam could be perfectly restored to its initial state of 34 mm after heating at 120 °C and removal of external force, indicating its exceptional shape memory properties. , Additionally, in Figure d, a rectangular-shaped foam could be temporarily reshaped into an “n” shape by heating it to 120 °C (above T g ). After cooling to room temperature, the foam maintained its temporary “n” shape.…”
Section: Resultsmentioning
confidence: 97%
“…53,54 As shown in Figure 5c, when compressed from its original diameter of 34 to 15 mm, it was observed that the EPC foam could be perfectly restored to its initial state of 34 mm after heating at 120 °C and removal of external force, indicating its exceptional shape memory properties. 55,56 Additionally, in Figure 5d, a rectangular-shaped foam could be temporarily reshaped into an "n" shape by heating it to 120 °C (above T g ). After cooling to room temperature, the foam maintained its temporary "n" shape.…”
Section: Mechanical and Thermal Properties Of Epc-xmentioning
Thermosetting foams have limited capabilities for recycling, reprocessing, or reshaping. Moreover, most of the foaming agents currently employed in these foams are derived from organic compounds sourced from petrochemicals, thereby posing a significant environmental threat due to heightened pollution. To solve these problems, a fully biobased degradable vitrimer foam (EPC-X) was fabricated using an environmentally friendly all-in-one foaming strategy by cross-linking epoxidized malepimaric anhydride (EMPA), 1,5diaminopentane (PDA), and 1,5-diaminopentane carbamate (PDAC) as a latent curing-blowing agent. To our delight, the vitrimer foams exhibit excellent mechanical properties (2.86 ± 0.11 MPa compressive strength) owing to their unique rigid rosin backbone and cross-linking networks. The presence of dynamic β-hydroxy ester bonds and the selfcatalytic behavior of tertiary amine groups facilitate network rearrangement without requiring additional catalysts, thereby resulting in the development of EPC-X with rapid self-healing and shape memory properties. The self-healing foam could support a weight of 500 g (approximately 562 times its own mass). Moreover, these high-performance vitrimer foams can also be easily degraded in an ethanolamine (EA) or NaOH solution under mild conditions. Such a design strategy offers an alternative approach for developing superior degradable and thermal stimuli-responsive thermosetting foams.
“…Specific 4D printed structures can respond to multiple stimuli based on the composition of the smart structure, which can be a smart composite or a smart material with different fillers. [ 171 ] We will only focus on physical and chemical stimulation, as little information is available regarding the 4D printing of biologically responsive materials.…”
Abstract4D (bio‐)printing endows 3D printed (bio‐)materials with multiple functionalities and dynamic properties. 4D printed materials have been recently used in biomedical engineering for the design and fabrication of biomedical devices, such as stents, occluders, micro‐needles, smart 3D‐cell engineered micro‐environments, drug delivery systems, wound closures, and implantable medical devices. However, the success of 4D printing relies on the rational design of 4D printed objects, the selection of smart materials, and the availability of appropriate types of external (multi‐)stimuli. Here, we first highlight the different types of smart materials, external stimuli, and design strategies used in 4D (bio‐)printing. Then, we present a critical review of the biomedical applications of 4D printing and discuss the future directions of biomedical research in this exciting area, including In vivo tissue regeneration studies, the implementation of multiple materials with reversible shape memory behaviors, the creation of fast shape‐transformation responses, the ability to operate at the microscale, untethered activation and control, and the application of (machine learning‐based) modeling approaches to predict the structure‐property and design‐shape transformation relationships of 4D (bio)printed constructs.This article is protected by copyright. All rights reserved
“…Compared with thermo‐active SMPs, electro‐active shape memory polymer composites (SMPCs) have the characteristics of easy control, remote drive and fast response, which made them more suitable for biomedical and micro‐level applications 15–17 . The electro‐active SMPCs is a composite material containing with conductive fillers such as graphene oxide, 18 carbon nanotubes (CNT), 19,20 carbon black, 21,22 carbon fiber, 23,24 and silver nanowires 25,26 . Among them, CNT have excellent thermal and electrical conductivity.…”
Section: Introductionmentioning
confidence: 99%
“…[15][16][17] The electro-active SMPCs is a composite material containing with conductive fillers such as graphene oxide, 18 carbon nanotubes (CNT), 19,20 carbon black, 21,22 carbon fiber, 23,24 and silver nanowires. 25,26 Among them, CNT have excellent thermal and electrical conductivity. Particularly, singlewalled carbon nanotubes (SWCNT) have the advantages of small diameter distribution range, few defects and high uniformity, which contribute to the excellent physical properties and chemical versatility of the materials.…”
Trans‐1,4‐polyisoprene/single wall carbon nanotubes nanocomposites (TPI/SWCNT) nanocomposites with thermo‐ and electro‐active shape memory performance were prepared via solution blending and vulcanization. Herein, the mechanical, thermo‐mechanical, electric conductivity properties, thermo‐ and electro‐active shape memory properties of pure TPI and TPI/SWCNT nanocomposites were investigated. It was demonstrated that the addition of SWCNT into the TPI matrix can improve its crystallinity, crystallization temperature and storage modulus characteristics, and form a two‐crystal melting peak. Compared with the pure TPI, the TPI/SWCNT nanocomposites need more time to recover to their initial shape under thermo stimulus, and the recovery ratio of TPI/SWCNT nanocomposites with 2.5 wt% SWCNT was about 92%. Moreover, pure TPI and TPI/SWCNT nanocomposites with SWCNT content of up to 2.0 wt% under 30 V could not recover under electro stimulus, but the TPI/SWCNT nanocomposites with 2.5 wt% SWCNT displayed electro‐active shape recovery property with a recovery ratio of 87.5%, because a certain amount of SWCNT can provide joule heat to melt the crystals completely and unfreeze cross‐linking network of TPI.
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