Cross-linking Of Chains Research Articles

Regulation of Glass Transition Temperature in Thermo‐Responsive Epoxy Shape Memory Polymers: The Roles of Chemical Crosslinking Density and Chain Flexibility

ABSTRACTShape memory polymers (SMPs) are novel kinds of smart materials whose shape can be changed in external conditions such as heat stimulus. Due to their excellent structural versatility and high elastic strain, they have important applications in the field of biomaterials. Here, a series of amorphous shape memory polymer materials are prepared and their shape memory properties and glass transition temperature (Tg) are also investigated. A special kind of epoxy polymer, whose shape can be changed at around physiological temperature, is synthesized by regulating the crosslinking density and introducing flexible aliphatic epoxy chains. The shape memory function of this epoxy polymer is studied by deformation test. In addition, to explore their application in the field of biomedical materials, the biocompatibility of the materials are evaluated, including the effects on the erythrocyte hemolysis rate and cell activity. The experimental results show that this kind of epoxy polymer has good shape memory function and biocompatibility.

Fabrication and Enhanced Flexibility of Starch-Based Cross-Linked Films.

The development of sustainable materials has driven significant interest in starch as a renewable and biodegradable polymer. However, the inherent brittleness, hydrophilicity, and lack of thermoplasticity of native starch limit its application in material science. This study addresses the limitations of native starch by converting it to dialdehyde starch (DAS) and cross-linking with polyether diamines via imine bonds. The effects of Jeffamine molecular weights (D-2000, D-400, and D-230) and mole ratios on the mechanical, thermal, and structural properties of starch-based films were examined. The cross-linked DAS/Js films exhibited significant enhancements in flexibility and toughness. Specifically, DAS/J2000 at a 0.03 mol ratio achieved a tensile strength of 62.9 MPa. In comparison, DAS/J400 at a 0.5 mol ratio demonstrated 126.2% elongation at break, indicating the balance between cross-linking density and chain mobility. X-ray diffraction (XRD) analysis revealed reduced crystallinity and tighter molecular packing with increased cross-linking. Dynamic mechanical analysis (DMA) indicated a decrease in Tg with an increasing mole ratio, reflecting enhanced molecular mobility. The results underscore the potential of optimized cross-linking conditions to produce starch-based films with properties that contribute to developing sustainable biopolymer materials.

Tailoring the Optical and Color Properties of Gamma Irradiated Polycarbonate/Cerium Oxide Nanocomposite Films for Their Application in Optoelectronic Devices

Nanocomposites (NC) of amorphous polycarbonate (PC) and cerium oxide (CeO2) nanoparticles (NPs) were prepared. The synthesized CeO2 had a nanonature of average particle size 22 nm, as indicated from their high resolution transmission electron microscopy images (HTEM). Samples of the PC/CeO2 NC films were irradiated with several γ ray doses (10-80 kGy). The resultant outcome of the γ irradiation on the optical properties of the NC films was studied using ultraviolet spectroscopy (UV-vis). Upon raising the γ ray dose up to 80 kGy, the maximum dose used, the direct bandgap decreased from 4.92 to 3.91 eV. The Urbach energy showed an opposite trend; it increased from 0.46 to 0.92 eV. This could be attributed to the domination of chain crosslinks. Also, the optical dielectric loss (ε”) assisted in identifying the nature of the microelectronic transitions. It was found that the PC/CeO2 NC films had direct allowed transitions. Additionally, the γ induced changes in the optical conductivity were studied. Moreover, the optical color changes between the pristine and the irradiated films were evaluated. The pristine NC film was uncolored. It showed significant color changes when irradiated with γ radiation up to 80 kGy. The induced modifications in the optical properties suggest that the γ radiation is an effective means for modifying the properties that allows the use of PC/CeO2 NC in optoelectronic devices.

Modification of chain extension and crosslinking structures of recycled polyester textile for 3D printing filament

AbstractThe increase in amount of polyester textile waste is contributing to the severity of environmental pollution because polyester cannot be easily recycled. To reduce the limits of its recyclability, a value‐added recycling approach should be explored. This work introduces an approach for recycling polyester textiles into 3D printable filaments. To increase recyclability of polyester textiles, the polyester materials are modified by ADR4468 additive. After the polyester is 3D printed, the sample with 1.0 wt% of ADR4468 shows the highest tensile and compressive strength properties compared with 1.5 and 2.0 wt%, owing to its fewer voids between the printed lines, a fish scale‐like morphology that spreads out, and a higher degree of crystallization. Moreover, the mechanism of modification suggests that ADR4468 extends and crosslinks the polyester chains by ring‐opening reactions of epoxy groups of ADR4468 and forms sea‐island structures. The sea‐island structures of bonded polyester branched cores with tangled polyester shell interface areas and unbonded polyester chain areas performed suitable rheological behaviors to recycle polyester textiles for 3D printable filaments production. The filaments can be used to replace commercially available filaments, offer a sustainable option for consumers, and impact both the polyester textile‐related recycling and 3D printing industries.Highlights An approach is proposed to recycle polyester textiles for 3D printing filament The approach uses a mechanical method to recycle polyester textiles Recycled polyesters were modified by ADR4468 to form core‐shell structures Core‐shell structures were separated by short polyesters(sea‐island structure) The structures met rheological behaviors for 3D printing filament

Sequential Irradiation Does Not Improve Fatigue Crack Propagation Resistance of Human Cortical Bone at 15 kGy

Sequential irradiation has been advocated for mitigating the reduction in fatigue properties of tendon compared to a single dose. However, to our knowledge, its capability of mitigating fatigue losses in bone is unknown. Recently, we reported that sequential irradiation did not mitigate losses in high-cycle S-N fatigue life of cortical bone at 15 kGy; however, it is unclear if sequential irradiation provides a benefit to fatigue crack propagation resistance. Our previous study also showed that radiation-induced collagen chain fragmentation and crosslinking increased from 0 to 15 kGy, suggesting that both likely contribute to the reduction in high-cycle S-N fatigue life within this dose range. Our objectives were: 1) to evaluate the fatigue crack propagation resistance of cortical bone and the effect of radiation on fracture plane damage zone thickness (DZT) at the crack tip in the dose range of 0 to 15 kGy, and 2) to evaluate whether sequential irradiation at 15 kGy mitigates the loss of fatigue crack propagation resistance of cortical bone compared to a single irradiation dose. Compact tension specimens from four male donor femoral pairs (ages 21-61 years old) were divided into 5 treatment groups (0 kGy, 5 kGy, 10 kGy, 15 kGy, and a 15 kGy sequential irradiation dose of 5 kGy sequentially irradiated with 10 kGy) and subjected to fatigue crack propagation testing (n=3-4 specimens per group) where fatigue crack growth rate da/dN and cyclic stress intensity factor ΔK were determined. Following testing, specimens were bulk stained in basic fuchsin, embedded in poly(methylmethacrylate), sectioned, and mounted on acrylic slides to evaluate fracture plane DZT at known crack lengths. Sections were then imaged with a fluorescence microscope, and fracture plane DZT was measured using ImageJ (n=3-4 specimens per group) and analyzed as a function of ΔK. We observed a decrease in fatigue crack propagation resistance at 15 kGy compared to doses of 10 kGy or lower (p≤0.013). Fracture plane DZT decreased overall with increasing radiation dose from 0 to 15 kGy. Sequential irradiation offered no improvement in fatigue crack propagation resistance (p=0.98). Radiation-induced collagen chain fragmentation and crosslinking in this dose range likely contribute to a decrease in energy dissipation capability with increasing radiation dose. Other alternative radiation sterilization methods besides sequential irradiation may be warranted to mitigate radiation-induced tissue damage and extend the functional lifetime of structural cortical bone allografts.

Mechanical characterization and structural analysis of elastodontic appliances under intraoral and artificial aging conditions

BackgroundThis study focused on the aging mechanism and degradation of mechanical and structural features of elastodontic appliances (EA) under artificial and intraoral aging to achieve oral myofunctional therapy with particular removable silicone elastomer devices.Materials and methodsEAs artificially aged in saliva with different pH values were investigated through cyclic compression testing along with characterization techniques (Scanning electron microscopy, X-ray diffraction, and Fourier transform infrared spectroscopy), and characterization analysis was also performed on clinically retrieved EAs.ResultsArtificial aging was found to have minimal effect on the structural properties of EAs, and intraorally aged samples showed perceptible micro-morphology. The Mullins index and peak stress decreased (P<0.01), while the compression set increased with prolonged aging time. Samples in alkaline saliva showed the largest Mullins effect (P<0.05).ConclusionsThe aging mechanism of the elastomer was found to be the crosslinking of main chains and scission of side chains. The presence of OH- enhanced the rupture degree of side bonds. The decline in viscoelastic properties was shown to be more severe with longer service durations.Clinical relevanceResearch on how the salivary environment and pH affect the aging characteristics of EAs is vital for guiding clinical applications and future modifications to extend their clinical lifetime.

Time-dependent constitutive behaviors of a dynamically crosslinked glycerogel governed by bond kinetics and chain diffusion

Soft materials featuring dynamic networks represent a burgeoning frontier in materials science, offering multifaceted applications spanning soft robotics, biomaterials, and flexible electronics. Unraveling the time-dependent constitutive behavior of these materials, rooted in dynamic networks, stands as a pivotal pursuit for engineering advancements. Herein, we fabricate a tough and extreme-temperature-tolerant glycerogel with a polymer network crosslinked by metal-coordination crosslinkers and conduct a thorough analysis of its intricate mechanical responses across monotonic loading, relaxation, creep, and cyclic tests. We then develop a physically grounded constitutive model integrating the dynamics of crosslinker association/dissociation and polymer chain diffusion, furnishing a holistic framework to elucidate their interplay. We employ a statistical description, using density functions of chains in terms of end-to-end vectors, to characterize network reconfiguration. The evolution of chain density under external load, mediated by crosslinker kinetics and chain diffusion in a viscous medium, leads to intriguing variations in elastic energy and stress responses. Through meticulous experimental validation and numerical simulations, we demonstrate the efficacy of the model in forecasting the mechanical behavior of dynamic polymer networks under diverse loading scenarios, encompassing strain rate effects, stress relaxation, Mullins effect, and self-recovery phenomena. Our findings provide valuable insights into the design and optimization of dynamic network-based materials for diverse applications in biomedical and engineering fields.

Silica-Based Composite Sorbents for Heavy Metal Ions Removal from Aqueous Solutions.

Weak polyelectrolyte chains are versatile polymeric materials due to the large number of functional groups that can be used in different environmental applications. Herein, one weak polycation (polyethyleneimine, PEI) and two polyanions (poly(acrylic acid), PAA, and poly(sodium methacrylate), PMAA) were directly deposited through precipitation of an inter-polyelectrolyte coacervate onto the silica surface (IS), followed by glutaraldehyde (GA) crosslinking and extraction of polyanions chains. Four core-shell composites based on silica were synthesized and tested for adsorption of lead (Pb2+) and nickel (Ni2+) as model pollutants in batch sorption experiments on the laboratory scale. The sorbed/desorbed amounts depended on the crosslinking degree of the composite shell, as well as on the type of anionic polyelectrolyte. After multiple loading/release cycles of the heavy metal ions, the maximum sorption capacities were situated between 5-10 mg Pb2+/g composite and 1-6 mg Ni2+/g composite. The strong crosslinked composites (r = 1.0) exhibited higher amounts of heavy metal ions (Me2+) sorbed than the less crosslinked ones, with less PEI on the surface but with more flexible chains being more efficient than more PEI with less flexible chains. Core-shell composites based on silica and weak polyelectrolytes could act as sorbent materials, which may be used in water or wastewater treatment.

Effects of Crystallinity and Branched Chain on Thermal Degradation of Polyethylene: A SCC-DFTB Molecular Dynamics Study.

As a widely used plastic, the aging and degradation of polyethylene (PE) are inevitable problems, whether the goal is to prolong the life of PE products or address the issue of white pollution. Molecular simulation is a vital scientific tool in elucidating the mechanisms and processes of chemical reactions. To obtain the distribution and evolution process of PE's thermal oxidation products, this work employs the self-consistent charge-density functional tight binding (SCC-DFTB) method to perform molecular simulations of the thermal oxidation of PE with different crystallinity and branched structures. We discovered that crystallinity does not affect the thermal oxidation mechanism of PE, but higher crystallinity makes PE more susceptible to cross-linking and carbon chain growth, reducing the degree of PE carbon chain breakage. The branched structure of PE results in differences in free volumes between the carbon chains, with larger pores leading to a concentrated distribution of O2 and chemical defects subsequently formed. The breakdown of PE is slowed down when chemical defects are localized in low-density regions of the carbon chain. The specifics and mechanism of PE's thermal oxidation are clearly revealed in this paper, which is essential for understanding the process in depth and for the development of anti-aging PE products.

Intrastrand Photo-Crosslinking of 5-Fluoro-2'-O-methyl-4-thiouridine-Modified Oligonucleotides and Its Implication for Fluorescence-Based Detection of DNA Sequences.

DNA photo-crosslinking reactions occur widely in biological systems and are often used as valuable tools in molecular biology. In this article, we demonstrate the application of an oligonucleotide 5-fluoro-2'-O-methyl-4-thiouridine (FSU)-containing probe for the fluorescent detection of specific DNA sequences. The design of the probe was predicated on studies of agents that could adversely affect its efficiency. The most important of these is the intrastrand photo-crosslinking of single-stranded oligodeoxynucleotides bearing FSU. Our research findings indicate that FSU after photoexcitation can react with nonadjacent bases; specifically, it can react with distant thymine and cytosine residues in the chain, forming fluorescent and nonfluorescent intrastrand crosslinks, respectively. In addition, partial photooxidation of the FSU residue to 5-fluorouridine was also observed. The results of the study are significant in terms of the use of FSU-labeled oligonucleotide probes in the fluorescence-based detection of specific DNA sequences because the creation of a fluorescent intrastrand crosslink could produce a false signal. To overcome this problem, replacing thymidine with deoxyuridine in the FSU-labeled oligonucleotide probe is proposed and tested.

A Discrete Four-Stranded β-Sheet through Catenation of M2L2 Metal-Peptide Rings.

Methods for precisely constructing a β-sheet assembly with number-defined strands in solution remains quite limited due to its intense aggregation property. Here, we report the precise construction of a four-stranded anti-parallel β-sheet by utilizing a non-covalent approach. This was achieved by folding and assembly of Ag+ and a pentapeptide (1) with the Ala-D3pa-Gly-3pa-Val (3pa: β-(3-pyridyl)-alanine) sequence, which was designed to form an interlocking Ag2(1)2 ring through metal cross-linking of the side chains. NMR analyses and X-ray crystallographic studies characterized the structure of the discrete β-sheet assembly as well as the remarkable structural selectivity in terms of strands' number, orientation and the sheet type.

Plasmon-Enhanced Multiphoton Polymer Crosslinking for Selective Modification of Plasmonic Hotspots.

A novel approach to selectively modify narrow subareas of metallic nanostructures adjacent to plasmonic hotspots, where strong electromagnetic field amplification occurs upon localized surface plasmon (LSP) excitation, is reported. In contrast to surface plasmon-triggered polymerization, it relies on plasmonically enhanced multiphoton crosslinking (MPC) of polymer chains carrying photoactive moieties. When they are contacted with metallic nanostructures and irradiated with a femtosecond near-infrared beam resonantly coupled with LSPs, the enhanced field intensity locally exceeds the threshold and initiates MPC only at plasmonic hotspots. This concept is demonstrated by using gold nanoparticle arrays coated with two specifically designed polymers. Local MPC of a poly(N,N-dimethylacrylamide)-based copolymer with an anthraquinone crosslinker is shown via atomic force microscopy. Additionally, MPC is tested with a thermoresponsive poly(N-isopropylacrylamide)-based terpolymer. The reversible thermally induced collapse and swelling of the MPC-formed hydrogel at specific nanoparticle locations are confirmed by polarization-resolved localized surface plasmon resonance (LSPR) spectroscopy. These hybrid metallic/hydrogel materials can be further postmodified, offering attractive characteristics for future spectroscopic/bioanalytical applications.

How Do Active Chain Density and Cross-Link Length Influence the Mullins Softening in Filled and Unfilled Natural Rubbers?

How Do Active Chain Density and Cross-Link Length Influence the Mullins Softening in Filled and Unfilled Natural Rubbers?

Preparation of high transparency, thermal stability, flame retardant polymethyl methacrylate nanocomposite via gamma-radiation polymerization

Achieving flame retardancy and thermal stability in poly(methyl methacrylate) (PMMA) while maintaining its inherent high transparency presents a significant challenge. In this work, we successfully fabricated an exceptional composite (P-SiO2-PMMA) with high transparency, flame retardancy, and thermal stability using 60Co γ-ray irradiation-induced copolymerization of methyl methacrylate (MMA), 2-hydroxyethyl 2-methyl-2-propenoate phosphate (HEMAP), and nano-silica (SiO2). The impact of the HEMAP on the crystal, optical, thermal stability, and combustion behavior properties of P-SiO2-PMMA has been investigated. P-SiO2/PMMA forms a three-dimensional network cross-linked molecular chain structure, enhancing the thermal decomposition temperature (Tdi), maximum thermal decomposition temperature (Tmax), glass transition temperature (Tg), and reducing the coefficient of thermal expansion (CTE). HEMAP and SiO2 significantly enhance the flame retardancy of the material. The limiting oxygen index (LOI) value of transparent flame-retardant 20-P-SiO2/PMMA composite material increased from 17.5% for PMMA to 23.2%, with a 47.3% decrease in peak heat release rate (PHRR). The flame retardant mechanism was also investigated. This study offers a novel approach for the industrial application of high transparency, thermal stability, and halogen-free flame-retardant PMMA composite.

Adsorption of silver ions onto chitosan hydrogel: Structural studies

Chitosan indicate a significant potential in the field of water treatment due to polymer high porosity, large specific surface area and its ability to bind strongly heavy metal ions form aqueous solutions. Therefore, chitosan based hydrogels have been fabricated by physical crosslinking of the polymer chains via sol–gel method using sodium β-glycerophosphate (β-GP) for silver ions (Ag) removal from water solutions. The aim of this study was to provide experimental studies under batch conditions to perform adsorption isotherm and evaluate the effect of silver adsorption onto chitosan hydrogel morphological and structural changes using SEM, XRD, FTIR and EDX analyses. Obtained results provides the data on the structural changes in the chitosan hydrogels under Ag adsorption process. The FTIR spectra confirmed that the C-NH2 and OH groups contribute to the formation of chitosan - silver ion complexes. The presence of adsorbed Ag in the samples < 0.8 gAgL−1 were evidenced by the characteristic peak at 2θ = 46.35°. Regarding to EDX analysis the adsorption efficiency toward Ag ions, rises with an increase in Ag initial concentration, resulting in L-type isotherm. The percentage removal of silver ions efficiency obtained 34 % for the highest Ag initial concentration (10 gAg L−1). SEM micrographs after Ag adsorption performed morphology as homogeneous porous network and reveals Ag present in the structure resulting from effective Ag adsorption. This study verified structural changes resulted from silver ions adsorption and confirmed the potential for thermosensitive chitosan hydrogels to applied as an adsorbent for water treatment applications.

Influence of Poly(Ethylene Glycol) Dimethacrylates’ Chain Length on Electrical Conductivity and Other Selected Physicochemical Properties of Thermally Sensitive N-isopropylacrylamide Derivatives

Thermosensitive polymers P1–P6 of N-isopropylacrylamide (PNIPA) and poly(ethylene glycol) dimethacrylates (PEGDMAs), av. Mn 550–20,000, were synthesized via surfactant-free precipitation polymerization (SFPP) using ammonium persulfate (APS) at 70 °C. The polymerization course was monitored by the conductivity. The hydrodynamic diameters (HDs) and the polydispersity indexes (PDIs) of the aqueous dispersion of P1–P6 in the 18–45 °C range, assessed via dynamic light scattering (DLS), were at 18° as follows (nm): 73.95 ± 19.51 (PDI 0.57 ± 0.08), 74.62 ± 0.76 (PDI 0.56 ± 0,01), 69.45 ± 1.47 (PDI 0.57 ± 0.03), 196.2 ± 2.50 (PDI 0.53 ± 0.04), 194.30 ± 3.36 (PDI 0.56 ± 0.04), 81.99 ± 0.53 (PDI 0.56 ± 0.01), 76.87 ± 0.30 (PDI 0.54 ± 0.01), respectively. The electrophoretic mobilities estimated the zeta potential (ZP) in the 18–45 °C range, and at 18 °C they were as follows (mV): −2.57 ± 0.10, −4.32 ± 0.67, −5.34 ± 0.95, −-3.02 ± 0.76, −4.71 ± 2.69, −2.30 ± 0.36, −2.86 ± 0.42 for polymer dispersion P1–P6. The polymers were characterized by attenuated total reflectance–Fourier transform infrared spectroscopy (ATR-FTIR), H nuclear magnetic resonance (1H NMR), thermogravimetric analysis (TG/DTA), Differential Scanning Calorimetry (DSC), and powder X-ray diffraction analysis (PXRD). The length of the cross-linker chain influences the physicochemical properties of the obtained polymers.

Effect of Phase Structure on the Viscoelasticity and Mechanical Properties of Isotactic Polypropylene Multicomponents Polymerized with Non-Conjugated α,ω-Diene.

Increasing of rubber content in isotactic polypropylene/ethylene-propylene rubber (iPP/EPR) alloys can extend the applications of this kind of polyolefin. The EPR content and phase structure of isotactic polypropylene multicomponents have great effect on the viscoelasticity and mechanical properties. iPP/EPR in-reactor alloys with a high EPR content were obtained through the in situ crosslinking of EPR chains with α,ω-diene. The morphological observation results indicate that the crosslinked iPP/EPR in-reactor alloys have a good spherical shape with clean and rough external surfaces. The high EPR content is finely dispersed in the crosslinked iPP/EPR alloys in areas ranging in size from tens of nanometers to several micrometers, which implies that a sufficient crosslinking degree of EPR chains can effectively prevent their aggregation and restrict macro-phase separation. The rheological results show a clear plateau in the terminal region, which reveals an entangled polymer chain network in the crosslinked iPP/EPR alloys. The well-dispersed EPR and the bi-continuous phase structure have a great effect on the mechanical properties of the isotactic polypropylene multicomponent which were assessed.

Molecular Chain Rearrangement-Induced In Situ Formation of Nanofibers for Improving the Strength and Toughness of Hydrogels.

Although poly(vinyl alcohol) (PVA) hydrogel has high elasticity and is suitable for cartilage tissue engineering, it is difficult to have both high strength and toughness. In this study, a simple and universal strategy is proposed to prepare strong and tough PVA hydrogels by in situ forming nanofibers on the original network structure induced by a molecular chain rearrangement. Quenching-tempering alteratively in ethanol and water several times is carried out to strengthen PVA hydrogels (PVA-Etn hydrogels) due to the advantages of noncovalent bonds in adjustability and reversibility. The results show that, after three quenching-tempering cycles, PVA-Et3 hydrogel with water content up to 79 wt % shows comprehensive improved mechanical properties. The compression modulus, tensile modulus, fracture strength, tensile strain, and tear energy of the PVA-Et3 hydrogel are 270, 250, 260, 130, and 180% of the initial PVA hydrogel, respectively. The improved mechanical properties of the PVA-Et3 hydrogel are attributed to the strong cross-linked PVA chains and hydrogen bond-reinforced nanofibers. This study not only provides a simple and efficient solution for the preparation of strong and tough polymer scaffolds in tissue engineering but also provides new insights for understanding the mechanism of improving the mechanical properties of polymer hydrogels by adjusting the molecular structure.

Regulation of surface oxygen functional groups in starch-derived hard carbon via pre-oxidation: A strategy for enhanced sodium storage performance

During the process of sodium storage in hard carbon anodes, the significance of surface oxygen functional groups cannot be overlooked. In this work, we utilize starch as raw material to synthesize hard carbon by the process of pre-oxidation and two-step carbonization. XPS analysis reveals that pre-oxidation bolsters the presence of CO bonds, thereby providing more active sites. TEM analysis reveals that hard carbon with pseudo-graphite and graphite-like structure is obtained at relatively high carbonization temperature (1400 °C), and the formation of closed pores results in lower specific surface area. The introduction of appropriate oxygen-containing groups in pre-oxidation process can facilitate the cross-linking of starch chains, promoting the increase of defect sites and the sodium storage performance of hard carbon. A series of samples are prepared at various pre-oxidation temperature. Among them, P200-HC obtained after pre-oxidation at 200 °C and carbonization at 1400 °C exhibits the highest reversible specific capacity of 342.7 mAh g−1 at current density of 0.1 C with an initial Coulombic efficiency of 71.1 %, and capacity retention of 87.3 % at current density of 1 C. The work presents a viable approach for the synthesis of hard carbon derived from starch, thereby expanding the design tactic of sodium-ion batteries with improved performance.

Competence of Carbonaceous Fibers/Nanofillers (Graphene, Carbon Nanotube) Reinforced Shape Memory Composites/Nanocomposites Towards Aerospace—Existent Status and Expansions

Abstract Shape memory or stimuli responsive polymers have established a unique grouping of smart materials. The technical merit of these polymers has been evaluated in aerospace sector, since last few decades. Particularly, the stimuli responsive polymers render inherent competences to recuperate the structural damages in exterior/interior space architectures. In this context, both the thermoplastics as well as thermosetting polymers depicted essential stimuli responsive behaviour. As interpreted in this state-of the-art review, the carbonaceous reinforcement like carbon fibers and nano-reinforcements including nanocarbons (graphene, carbon nanotube) have been employed in the shape recovering matrices. The performance of ensuing shape retrieving aerospace materials was seemed to be reliant on the polymer chain crosslinking effects, filler/nanofiller dispersal/alignment, microstructural specs, interfacial contour and interactions, and processing techniques used. Consequently, the shape actuations of polymer/carbon fiber composites were found to be instigated and upgraded through the inclusion of nanocarbon nano-additives. The ensuing high-tech shape memory composites/nanocomposites have anomalous significance for various aero-structural units (fuselage, wings, antennas, engines, etc.) due to prevention of possible thermal/shock/impact damages. Future implications of carbonaceous shape memory composites/nanocomposites in aerospace demands minimizing the structure-property-performance challenges and large scale fabrication for industrial scale utilizations. In this way, deployment of carbonaceous nanofiller/filler based composites revealed enormous worth due to low density, anti-fatigue/wear, anti-corrosion, non-flammability, self-healing, and extended durability and long life operations. However, there are certain challenges associated with the use of nanocarbons and ensuing nanocomposites in this field markedly the adoption of appropriate carbon fiber coating technique, aggregation aptitude of nanocarbons, additional processing steps/cost, nanoparticle initiated invisible defects/voids, difficulty in machinability operations due to presence of nanoparticles, and corrosion risk of composite structures in contact with metal surfaces. By overcoming these hinderances, nanoparticles modified carbon fiber based composites can be promising towards a new look of upcoming modernized aerospace industry.