High Performance Polymers

A symmetrical dicyclopentyl substituted cucurbit[6]uril (CyP₂Q[6]) was synthesized, and crystallized under the conditions of 3 mol/L hydrochloric acid solution and the induction of ZnCl₂. The crystal structure was characterized by X-ray single crystal diffractometer, ¹H NMR and MS, and the results show that the crystal belongs to the monoclinic crystal system with P2₁/n space group, a = 13.095 (2), b = 33.002 (6), c = 15.770 (3), α = 90°, β = 102.828(5)°, γ = 90°, Z = 4, and a macroporous honeycomb structure appears in the crystal.

The design of lightweight neutrons shields has been restricted for quite some time to the use of the epoxy thermosets as the main building blocks. Meanwhile, the recent developments in the field of polymers suggest otherwise. Indeed, benzoxazine resins have taken the lead over the traditional thermosets in many exigent applications. Therefore, in a vision to introduce newer matrices with better performances and to further expand the applications of the benzoxazine resins into the nuclear field, the neutron shielding efficiency along with the thermal and thermomechanical performances of the neat benzoxazine polymer and its subsequent B₄C-reinforced composites were investigated. The neutron shielding measurements were performed using an optimized experimental setup at NUR research reactor, Algiers. The neat benzoxazine polymer displayed almost similar thermal neutrons screening performances than the epoxy with a macroscopic cross-section (Σ) of a 0.724 cm⁻¹ equivalent to a mean free path (λ) of 0.957 cm. The effect of the particle amount was also studied to maximize the shielding ability of the developed materials. For instance, the benzoxazine composite containing 20 wt.% of B₄C displayed the outstanding screening ratio of about 96% for a sample thickness of 13 mm. Finally, the remarkable findings were put into context by providing multifaceted comparisons with the available shielding materials.

Free-standing flexible supercapacitive electrodes have practical application for wearable energy storage devices. In this paper, graphene paper (GP), a flexible electrode substrate, was prepared by one-step reduction of graphene oxide (GO) using HI solution. GP can be used independently as a flexible electrode with specific capacitance of 227 F/g. In order to make up for the shortage of GP specific capacitance storage, polyaniline (PANI) with high specific capacitance and good electrical conductivity was selected to composite with GP by electrochemical polymerization approach. This method to fabricate electrode material by direct electrochemical polymerization avoids the use of conductive binder and organic solvent. Owing to the specific capacitance contribution of PANI and GP, the PANI/GP composites exhibit higher specific capacitance when the polymerization time is 30 s and the polymerization voltage is 0.8 V. At 1 A/g current density, the specific capacitance of composite is up to 759 F/g, which is 3.34 times of neat GP.

The polymers with pH responsiveness and temperature sensitivity exhibit important applications in many fields. To endow the responsive polymers with self-healing is meaningful work, which contributes to increase their service life and reduce waste of resources significantly. In this research, a series of pH-responsive polyurethanes containing dynamic disulfide bonds and carboxylic acid functional groups were prepared by mixing polycaprolactone diol (PCL), hexamethylene diisocyanate (HDI), 2,2-dimethylolbutyric acid, and bis(2-hydroxyethyl) disulfide. The structure of the polymer was confirmed by some characterization methods such as infrared absorption spectroscopy, Raman scattering spectroscopy, X-ray diffraction, and differential scanning calorimetry. Many performances of the polymer such as the contact angle, thermal stability, mechanics, and self-healing properties can be adjusted by changing the functional units of polyurethanes. The dynamic disulfide bonds in the main chain were observed no harm to the pH response performance, instead which were beneficial to the promotion of heat resistance, tensile properties, and self-healing performance of polyurethane. The elongation at break and the tensile strength are increased by 85.3% and 54.9%, respectively. All the polyurethane exhibited considerable self-healing effects at 110°C, with the highest healing efficiency reaching 93.7%, as a result of the dissociation of hydrogen bonds and the exchange reaction of disulfide bonds.

The residual stress of metal liners wrapped by composite materials has a significant influence on the service performance of rotating parts, such as flywheel rotors and motor jackets. However, the deformation of the liners, the flow of resins, and the temperature variation during the winding process make it difficult to predict and control this residual stress. In this paper, the process-induced strains were monitored online by a strain gauge with the help of a wireless strain meter. The evolution of this strain during the manufacturing process was fully discussed. A rapid curing resin system was used and its curing properties were tested by differential scanning calorimetry. The mechanical properties of the resin matrix and its composite were characterized. The effect of the curing cycle on the evolution of the residual strain was discussed in detail through comparative experiments. The experimental results show that the use of infrared radiation has a significant advantage regarding residual stress accumulation. This advantage is greater when carbon fiber is used than when glass fiber is used. The prestress in composites of glass fiber and carbon fiber increases by 5.9% and 41.7%, respectively, after cooling.

In this article, pure epoxy resin and silica–epoxy nanocomposite models were established to investigate the effects of hyperbranched polyester on microstructure and thermomechanical properties of epoxy resin through molecular dynamics simulation. Results revealed that the composite of silica can improve the thermomechanical properties of nanocomposites, including the glass transition temperature, thermal conductivity, and elastic modulus. Moreover, the thermomechanical properties were further enhanced through chemical modification on the silica surface, where the effectiveness was the best through grafting hyperbranched polyester on the silica surface. Compared with pure epoxy resin, the glass transition temperature of silica–epoxy composite modified by silica grafted with hyperbranched polyester increased by 38 K. The thermal conductivity increased with the increase of temperature and thermal conductivity at room temperature increased to 0.4171 W/(m·K)⁻¹ with an increase ratio of 94.3%. Young’s modulus, volume modulus, and shear modulus all fluctuated as temperature rise with a down overall trend. They increased by 44.68%, 29.52%, and 36.65%, respectively, when compared with pure epoxy resin. At the same time, the thermomechanical properties were closely related to the microstructure such as fractional free volume (FFV), mean square displacement (MSD), and binding energy. Silica surface modification by grafting hyperbranched polyester reduced the FFV value and MSD value most and strengthened the combination of silica and epoxy resin matrix the best, resulting in the best thermomechanical properties.

This article presents the mechanical, physical, and tribological properties of the boron carbide (B₄C) reinforced epoxy matrix composites (BEMCs). The BEMC samples were prepared with various B₄C concentration of 0%, 1%, 2%, 3%, and 5%. B₄C particles were treated with a silane coupling agent to ensure efficient adhesion with epoxy. The influence of a range of parameters (particle loading, sliding speed, sliding distance, and normal load) on the wear and friction behavior of BEMCs were evaluated by conducting wear tests under dry sliding conditions on a pin-on-disc wear test set-up. The addition of B₄C to the epoxy polymer improved the wear resistance of the composites. Maximum wear resistance and coefficient of friction were observed for the composite with the highest percentage of B₄C (5%). The specific wear rate was reduced on increasing load and sliding distance and increased with the sliding velocity. Mechanical properties including compression strength, flexural strength, and impact energy, along with physical properties such as density and hardness, were also evaluated. B₄C particles improved the hardness, density, flexural and compression strength, and impact resistance of the composites. Scanning electron microscope (SEM) analysis of the worn-out surfaces and flexural fractured surfaces was carried out to predict the possible wear and fracture mechanisms. Micro-ploughing, abrasion, and adhesion were the wear mechanisms in BEMCs. Under the flexural loads, particulate de-bonding, pull-out, and brittle fracture of the matrix were the governing failure mechanisms.

Poly(vinylidene fluoride) (PVDF)-based composites attract tremendous attention as dielectric materials. However, their development has been limited due to the raised problem in the in-homogeneous polymer composites. In this work, a novel PVDF-based film incorporated with polyamide-1, containing the highest density of dipole among all polyamides, was prepared to improve the crystallization behaviors and dielectric properties. The results showed that the optimal concentration of polyamide-1 in PVDF was 6 wt.%. The crystallization rate of PVDF was improved in the presence of polyamide-1. Interestingly, the polyamide-1 was conductive to the formation of β form crystal of PVDF, which exhibited great electric performance. The dielectric constant of PVDF increased sharply and loss tangent still kept at a low level of 0.03@100 Hz when the concentration of polyamide-1 was 6 wt.%. This work may provide a new direction to design dielectric materials for PVDF blends.

A kind of modified bismaleimide resin, with good processability, heat resistance, and impact strength was developed, using 4,4^′-dipropargyloxydiphenyl ether (DPEDPE), N-(4-propargyloxyphenyl)maleimide (4-PPM), and 3-ethynylphenyl maleimide (3-EPM) as modifiers. The DPEDPE, 4-PPM, and 3-EPM were synthesized and characterized by Fourier transform infrared spectroscopy (FTIR) and ¹H-nuclear magnetic resonance (¹H NMR), and used to modify the N,N^′-(4,4^′-diphenylmethane)bismaleimide (BDM)/2,2^′-diallyl bisphenol A (DABPA) resin system (BD) to obtain the different blend resin systems of DPEDPE-modified BD (BDD), 4-PPM-modified BD (BDP), and 3-EPM-modified BD (BDE). The curing temperature of BD resin increases with increase of the alkynyl-terminated modifier content. The processability of BD resin was improved with addition of the propargyloxy-terminated compounds. The temperature of 5% weight loss, residual yield at 800°C and glass transition temperature of the cured BD resin increase with increase of the alkynyl-terminated modifier content and can reach 443°C, 46.7% and higher than 380°C. The tensile strength of the cured BD resin decreases with increase of alkynyl-terminated modifier content. The impact strength of the cured BD resin increases with increase of the propargyloxy-terminated compound content and can increase by 65%. The tensile strength, elastic modulus, and impact strength of the cured BD resin blended with DPEDPE can be 73.7 MPa, 4.1 GPa, and 19.6 kJ m⁻², respectively. Moreover, the cured BD resin blended with DPEDPE has good water absorption resistance.

Drawing self-cleaning technology into polymer membranes offers an extensive solution to overcome the membrane fouling obstacle. Herein, the GO-ZnO-Ag nano-hybrid particles with photocatalytic activity prepared via the microwave hydrothermal method were immobilized in poly(m-phenylene isophthalamide) (PMIA) membranes. Not only was the thorny issue in catalyst recovery avoided, but also the satisfactory photocatalytic self-cleaning performance of the polymer membrane was awarded. GO and noble metal silver nanoparticles (AgNPs) acted as a conductive electron transfer carrier and an electron host, respectively, which hindered the recombination rate of excited electrons and holes on ZnO under UV light. The UV-driven PMIA membrane photodegradation rates of MB and Cr(VI) were up to 97.2% and 94.3%, respectively, at 150 min on photodegradation kinetics. Also, MB was completely degraded at 180 min. For MB and Cr(VI) mix solutions, their degradation efficiencies were 78.1% and 71%, respectively. The BSA rejection rate of the modified polymer membrane was 93.8%, and the water flux was 408.8 (L·m⁻²·h⁻¹). Permeability was maintained at a high level after repeated use. Therefore, the newly designed PMIA/GO-ZnO-Ag series membranes could expand the application of polymers in wastewater disposal industry.

Polymer adhesives are widely used in daily applications and in industry owing to their flexibility and overall non-toxicity, particularly in interfacial adhesion. The spreading of polymer adhesives on adherend is one of the essential considerations for the interfacial adhesion of polymer adhesives, which is strongly related to their wetting behaviors. While relationships between polymer microstructure and adhesion have been investigated in previous studies, it remains challenging to unveil the effect of polymer microstructure on wettability. To address this issue, here we utilize coarse-grained molecular dynamics (CGMD) simulations to systematically elucidate how the wettability of a polymer adhesive droplet on a surface depends on bending stiffness. The wetting dynamics and the contact angle are studied to show the evolution of morphology of droplets during the wetting process. The results indicate the wettability is weakened by the increase of bending stiffness of polymer chain. Detailed thermodynamic property analysis is further conducted, revealing that the adhesion between the polymer droplet and substrate deteriorates due to the decline of wettability. Interestingly, we observe such deterioration becomes more significant by both increasing the temperature and decreasing the bending stiffness. Our study sheds light on the dependence of chain bending stiffness and temperature on the wetting behavior of polymer adhesive droplets, and offers insights, which, upon experimental validation can then be used for the design of adhesives or hydrogels.