Durable Biopolymer Films From Lignin-Carbohydrate Complex Derived From a Pulp Mill Side Stream

Valorization of side streams offers novel types of raw materials to complement or replace synthetic and food-based alternatives in materials science, increasing profitability and decreasing the environmental impacts of biorefineries. Lignocellulose biomass contains lignin and carbohydrates that are covalently linked into lignin-carbohydrate complexes (LCCs). In biomass fractionation processes, these complexes are conventionally considered as waste, which hinders the biomass fractionation process, and they may solubilize into aqueous effluents. This study presents how LCCs, derived from pulp mill effluent, can be turned into valuable biopolymers for industrial polymer film applications. Free-standing composite films containing hydroxyethyl cellulose (HEC) and LCCs with varying molar mass, charge density and lignin/hemicellulose ratio were prepared to study the effect of LCC amount on mechanical properties and oxygen permeability. Increasing the LCC content increased the yield point and Young’s modulus of the films. Breaking strain measurements revealed a non-linear correlation with the LCC concentration for the samples with higher lignin than hemicellulose content. The addition of LCC enhanced oxygen barrier properties of HEC films significantly even at high relative humidity. The present research demonstrates how a currently underutilized fraction of the biorefinery side stream has the potential to be valorized as a biopolymer in industrial applications, for example as a barrier film for paper and board packaging.

Mechanically Robust Flexible Multilayer Aramid Nanofibers and MXene Film for High-Performance Electromagnetic Interference Shielding and Thermal Insulation

In order to overcome the various defects caused by the limitations of solid metal as a shielding material, the development of electromagnetic shielding materials with flexibility and excellent mechanical properties is of great significance for the next generation of intelligent electronic devices. Here, the aramid nanofiber/Ti3C2Tx MXene (ANF/MXene) composite films with multilayer structure were successfully prepared through a simple alternate vacuum-assisted filtration (AVAF) process. With the intervention of the ANF layer, the multilayer-structure film exhibits excellent mechanical properties. The ANF2/MXene1 composite film exhibits a tensile strength of 177.7 MPa and a breaking strain of 12.6%. In addition, the ANF5/MXene4 composite film with a thickness of only 30 μm exhibits an electromagnetic interference (EMI) shielding efficiency of 37.5 dB and a high EMI-specific shielding effectiveness value accounting for thickness (SSE/t) of 4718 dB·cm2 g−1. Moreover, the composite film was excellent in heat-insulation performance and in avoiding light-to-heat conversion. No burning sensation was produced on the surface of the film with a thickness of only 100 μm at a high temperature of 130 °C. Furthermore, the surface of the film was only mild when touched under simulated sunlight. Therefore, our multilayer-structure film has potential significance in practical applications such as next-generation smart electronic equipment, communications, and military applications.

Effect of Crosslinkers on Optical and Mechanical Behavior of Chiral Nematic Liquid Crystal Elastomers

Chiral nematic (N*) liquid crystal elastomers (LCEs) are suitable for fabricating stimuli-responsive materials. As crosslinkers considerably affect the N*LCE network, we investigated the effects of crosslinking units on the physical properties of N*LCEs. The N*LCEs were synthesized with different types of crosslinkers, and the relationship between the N*LC polymeric system and the crosslinking unit was investigated. The N*LCEs emit color by selective reflection, in which the color changes in response to mechanical deformation. The LC-type crosslinker decreases the helical twisting power of the N*LCE by increasing the total molar ratio of the mesogenic compound. The N*LCE exhibits mechano-responsive color changes by coupling the N*LC orientation and the polymer network, where the N*LCEs exhibit different degrees of pitch variation depending on the crosslinker. Moreover, the LC-type crosslinker increases the Young’s modulus of N*LCEs, and the long methylene chains increase the breaking strain. An analysis of experimental results verified the effect of the crosslinkers, providing a design rationale for N*LCE materials in mechano-optical sensor applications.

Effects of Electron Beam Irradiation on 3D-Printed Biopolymers for Bone Tissue Engineering

Implanting scaffolds designed for the regeneration or the replacement of bone tissue damaged by diseases and injuries requires specially designed biomaterials that promote cell adhesion. However, the biodegradation rate of these scaffolds based on a single material is uniform. Four-dimensional printing appears to be a promising method to control this aspect by changing the shape and/or the intrinsic properties of 3D-printed objects under the influence of external stimuli. Two main classes of biomaterials and biocomposites based on biopolyesters, namely poly(lactic acid) (PLA) and poly(caprolactone) (PCL), were used in this study. Each of them was mixed with the inorganic filler hydroxyapatite (HA), which is a component of natural bone. The biocomposites and biomaterials were prepared using the melt extrusion process and then shaped using a 3D printer. Three-dimensional specimens showed a decrease in elongation at break and breaking strain due to variations of crystallinity. The crystallinity of irradiated samples increased slightly with irradiation and a new crystalline phase was observed in the case of the PLA. Four-dimensional printing of biomaterials using electron radiation shows great promise for bone tissue engineering based on biocomposite scaffolds and other medical applications.

Elucidation of Mechanical, Physical, Chemical and Thermal Properties of Microbial Composite Films by Integrating Sodium Alginate with Bacillus subtilis sp.

Materials are the foundation in human development for improving human standards of life. This research aimed to develop microbial composite films by integrating sodium alginate with Bacillus subtilis. Sodium alginate film was fabricated as control. The microbial composite films were fabricated by integrating 0.1, 0.2, 0.3, 0.4, 0.5 and 0.6 g of Bacillus subtilis into the sodium alginate. Evaluations were performed on the mechanical, physical, chemical and thermal properties of the films. It was found that films reinforced with Bacillus subtilis significantly improved all the mentioned properties. Results show that 0.5 g microbial composite films had the highest tensile strength, breaking strain and toughness, which were 0.858 MPa, 87.406% and 0.045 MJ/m3, respectively. The thickness of the film was 1.057 mm. White light opacity, black light opacity and brightness values were 13.65%, 40.55% and 8.19%, respectively. It also had the highest conductivity, which was 37 mV, while its water absorption ability was 300.93%. Furthermore, it had a higher melting point of 218.94 °C and higher decomposition temperature of 252.69 °C. SEM also showed that it had filled cross-sectional structure and smoother surface compared to the sodium alginate film. Additionally, FTIR showed that 0.5 g microbial composite films possessed more functional groups at 800 and 662 cm-1 wavenumbers that referred to C–C, C–OH, C–H ring and side group vibrations and C-OH out-of-plane bending, respectively, which contributed to the stronger bonds in the microbial composite film. Initial conclusions depict the potential of Bacillus subtilis to be used as reinforcing material in the development of microbial composite films, which also have the prospect to be used in electronic applications. This is due to the conductivity of the films increasing as Bacillus subtilis cell mass increases.

Transparent, Conductive Hydrogels with High Mechanical Strength and Toughness

Transparent, conductive hydrogels with good mechanical strength and toughness are in great demand of the fields of biomedical and future wearable smart electronics. We reported a carboxymethyl chitosan (CMCS)–calcium chloride (CaCl2)/polyacrylamide (PAAm)/poly(N-methylol acrylamide (PNMA) transparent, tough and conductive hydrogel containing a bi-physical crosslinking network through in situ free radical polymerization. It showed excellent light transmittance (>90%), excellent toughness (10.72 MJ/m3), good tensile strength (at break, 2.65 MPa), breaking strain (707%), and high elastic modulus (0.30 MPa). The strain sensing performance is found with high sensitivity (maximum gauge factor 9.18, 0.5% detection limit), wide strain response range, fast response and recovery time, nearly zero hysteresis and good repeatability. This study extends the transparent, tough, conductive hydrogels to provide body-surface wearable devices that can accurately and repeatedly monitor the movement of body joints, including the movements of wrists, elbows and knee joints. This study provided a broad development potential for tough, transparent and conductive hydrogels as body-surface intelligent health monitoring systems and implantable soft electronics.

Siloxane Matrix Molecular Weight Influences the Properties of Nanocomposites Based on Metal Complexes and Dielectric Elastomer

Siloxane-based elastomers are some of the most sought-after materials for the construction of actuators and equipment for energy harvesting devices. This article focuses on changes of the mechanical (breaking stress, breaking strain, Young’s modulus) and dielectric properties for elastomers prepared with silicones, induced by the variation of molecular weight of the matrix, with three different silicone polymers having 60,000 g/mol, 150,000 g/mol, and 450,000 g/mol (from GPC measurements). Multiple siloxane elastomers were crosslinked with methyltriacetoxysilane using the sol-gel route. The dielectric permittivity values of the elastomers were also enhanced with two different complex structures containing siloxane bond and 3d transition metals as filler materials for polydimethylsiloxane polymers with various molecular weights. The dielectric spectroscopy tests demonstrated a small decrease (5%) for the values of the dielectric permittivity in relation to increased molecular weight of the siloxane polymer, both for samples prepared with pure polymer and for samples with metal complexes. The samples of nanocomposites showed a >50% increase of dielectric permittivity values relative to samples prepared of pure siloxane elastomer. The thermal tests demonstrated that the nanocomposites retained thermal stability similar with samples prepared of pure siloxane elastomer. The behavior under controlled conditions of humidity showed a trend of increased water vapor sorption with increasing molecular weight but an overall hydrophobic stable character of nanocomposites.

Study of Mechanical Properties of 3D Printed Material for Non-Pneumatic Tire Spoke

The spokes of airless tire or non-pneumatic tire (NPT) are normally made with thermoplastic polyurethane (TPU), which is highly elastic material, to replace inflation pressure in conventional pneumatic tire. However there are limitation in designing of complex spoke geometries due to difficulty in manufacturing process, which normally involve molding process. Recently, the 3D printing technique has been improved and can be used to create highly complex geometries with wide range of materials. However the mechanical properties of printed spoke structure using 3D printing technique are still required to design and development of NPT. This research aim to study the mechanical properties of TPU while varying in printing conditions. The specimens were prepared from actual NPT spoke using waterjet cutting technique and 3D printing technique according to the testing standard ASTM D412 and D638, respectively. The tensile tests were performed on the specimens with corresponding crosshead speed. The testing speed of 3D printed specimen were also varied to 100 and 200 mm/min to study the effects of strain rate on mechanical properties. The stress-strain relationships were obtained from tensile testing and the important mechanical properties were then evaluated. The mechanical properties of specimens prepared from actual NPT spokes and 3D printed specimens were then compared. The ultimate stress of specimens prepared from actual NPT spokes in radial direction and 3D printed specimens with 100% infill were found to be 32.92 and 25.47 MPa, respectively, while the breaking strain were found to be 12.98 and 10.87, respectively. Thus, the information obtained from this research can be used to ensure the possibility in creating NPT spoke using 3D printing technique based on elastic material such as TPU.

Influence of re-entrant hexagonal structure and helical auxetic yarn on the tensile and auxetic behavior of parametric fabrics

This paper focuses on systematically analyzing the influence of macro fabric structure and yarn architecture on the mechanical and auxetic performance of parametric auxetic fabrics. Re-entrant hexagonal (REH) and helical auxetic yarn (HAY) were adopted as a macro fabric structure and weft yarn to produce three kinds of auxetic fabrics: REH fabric with HAY as weft yarn (REH-HAY); REH fabric with elastic yarn as weft yarn (REH-1, REH-2, REH-3); and plain fabric with HAY as weft yarn (NREH-HAY). By controlling the existence of the HAY and REH structure, the influence of the REH structure and HAY on the mechanical and auxetic properties was thoroughly analyzed. It is demonstrated that both the REH macrostructure and HAY micro configuration can contribute to the performance of the auxetic fabric. Specifically, in the presence of the REH structure and HAY, the auxeticity was found to a 77% increase compared with NREH-HAY and the breaking strain and load rises by about 37.50% and 90.42%, respectively. Notably, the variation of the polyurethane (PU) weft yarn per unit length influenced the tensile and auxetic performance to a lesser extent, while by changing PU to HAY, a significant increase of negative Poisson’s ratio value from –1.155 to –1.492 was noticed without greatly jeopardizing the stretchability. Furthermore, the cyclic tensile results demonstrate the stability and elasticity of the fabric. The comparative analysis can give guidance to optimize fabric design and inspire the innovative design of the auxetic textiles, all of which will pave the way for a quantitative and optimizing design for auxetic textiles.

Silica Nanoparticles Reinforced Ionogel as Nonvolatile and Stretchable Conductors

Ionogels combine the advantages of being conductive, stretchable, transparent and nonvolatile, which makes them suitable to be applied as conductors for flexible electronic devices. In this paper, a series of ionogels based on 1-ethyl-3-methylimidazolium ethyl-sulfate ([C2mim][EtSO4]) and polyacrylic networks were prepared. Silica nanoparticles (SNPs) were dispersed into the ionogel matrix to enhance its mechanical properties. The thermal, mechanical and electrical properties of the ionogels with various contents of crosslinking agents and SNPs were studied. The results show that a small amount of SNP doping just increases the breaking strain/stress and the nonvolatility of ionogels, as well as maintaining adequate conductivity and a high degree of transparency. Furthermore, the experimental results demonstrate that SNP-reinforced ionogels can be applied as conductors for dielectric elastomer actuators and stretchable wires, as well as for signal transmission.