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Polymeric hydrogels have drawn considerable attention as a biomedical material for their unique mechanical and chemical properties, which are very similar to natural tissues. Among the conventional hydrogel materials, self-healing hydrogels (SHH) are showing their promise in biomedical applications in tissue engineering, wound healing, and drug delivery. Additionally, their responses can be controlled via external stimuli (e.g., pH, temperature, pressure, or radiation). Identifying a suitable combination of viscous and elastic materials, lipophilicity and biocompatibility are crucial challenges in the development of SHH. Furthermore, the trade-off relation between the healing performance and the mechanical toughness also limits their real-time applications. Additionally, short-term and long-term effects of many SHH in the in vivo model are yet to be reported. This review will discuss the mechanism of various SHH, their recent advancements, and their challenges in tissue engineering, wound healing, and drug delivery. [ABSTRACT FROM AUTHOR]

In this paper, we present an extensive experimental study on the dynamic mechanical properties of composites with polymer matrices, as well as a quantification of the parameters that influence these properties. Polymer-composite matrices make it possible to form any reinforcement arrangement of fibres, particles, and layers, which makes it possible to form composite materials with certain dominant mechanical properties according to the internal arrangement for the application. In this study, we focused on the dynamic properties (i.e., damping parameters, such as the loss factor (tan d), logarithmic decrement (λ), storage modulus (E′), and loss modulus (E″)) of composites with polymer matrices, including parameters such as the fibre material, fabric weaving, fibre orientation, temperature, frequency, particle size, volume of short fibres, and epoxy resin type. If other articles focus on one type of composite and 1–2 parameters, then the benefit of this article lies in our analysis of 8 mentioned parameters in the experimental analysis of 27 different types of composites with polymer matrices. The tested fibre materials were glass, aramid, and carbon; the tested woven fabrics were twill, plain, unidirectional, and satin; the temperature range was from −50 to +230 °C; the frequency was 1 Hz and 10 Hz; the particle size was 0.1–16 mm; the volume percentages of the short fibres were 3, 6, and 12 vol.% of the hybrid polymer composites and the type of polymer matrix. We used the free-damped-vibration method with vibration dynamic signal analysis and the forced-damped vibration of dynamic mechanical thermal analysis for testing. We ranked the parameters that influence the dynamic vibration properties according to the effects. Among sets of results provided in the paper, considering the storage modulus, loss modulus, and loss factor, the best results of the fibre composites were for aramid-fibre-reinforced polymers, regardless of the weave type, with an advantage for unidirectional fabric. The best results of the particle composites were for those with fine filler sizes that incorporated the short fibres. [ABSTRACT FROM AUTHOR]

Mechanical properties of the extracellular matrix have a profound effect on the behavior of anchorage-dependent cells. However, the mechanisms that define the effects of matrix stiffness on cell behavior remains unclear. Therefore, the development and fabrication of synthetic matrices with well-defined stiffness is invaluable for studying the interactions of cells with their biophysical microenvironment in vitro. We demonstrate a methoxypolyethylene glycol (mPEG)-modified chitosan hydrogel network where hydrogel stiffness can be easily modulated under physiological conditions by adjusting the degree of mPEG grafting onto chitosan (PEGylation). We show that the storage modulus of the hydrogel increases as PEGylation decreases and the gels exhibit instant self-recovery after deformation. Breast cancer cells cultured on the stiffest hydrogels adopt a more malignant phenotype with increased resistance to doxorubicin as compared with cells cultured on tissue culture polystyrene or Matrigel. This work demonstrates the utility of mPEG-modified chitosan hydrogel, with tunable mechanical properties, as an improved replacement of conventional culture system for in vitro characterization of breast cancer cell phenotype and evaluation of cancer therapies. [ABSTRACT FROM AUTHOR]

In this study, magnetorheological elastomer (MRE) was fabricated using an electromagnetic device with a new configuration mold at the orientation of 0°, 45° and 90°. This new curing concept enhanced the alignment of carbonyl iron particles (CIPs) within the silicone matrix in the presence of silicone oil (SO) during solidifying, by eliminating air gaps to prevent magnetic flux losses. Using a mold made of steel, which is a magnetic material, the mold functions as a guide for concentrated magnetic flux of 0.315 T to pass through the MRE sample. Scanning electron microscopy (SEM) was used to observe the surface morphology of the fabricated MRE samples particularly the alignment of the CIPs. The field-dependent dynamic properties of the MREs were measured using a rheometer. The analysis implied that the effectiveness of the MRE operating under shear deformation with this curing concept provided the highest magneto-induced modulus of 1.01 MPa when a 45° orientation mold is used, with relative magnetorheological (MR) effect value up to 918%, followed by 0° mold orientation with 0.79 MPa magneto-induced modulus and 646% relative MR effect. The high modulus properties offered by this MRE are believed to be potentially useful in industrial applications where a high range of stiffness is required particularly in the shear direction. [ABSTRACT FROM AUTHOR]

It has previously been shown that optimum particle size distributions with a maximum packing fraction can be achieved from a straight line plot of the accumulated sum of particle volume fractions versus the square root of particle size. This study addresses practical limits for two dominant fundamental approaches to designing particle size distributions to address the effect on a specific physical property such as viscosity. The two fundamental approaches to obtain such a straight line would include: the first design approach would be generated utilizing the same initial particle size, Dmin, but by using different ultimate particle sizes, Dmax. The second design approach would be generated where each distribution starts with the same initial particle size, Dmin, and ends with the same ultimate particle size, Dmax. The first design approach is particularly useful to identify the possible slopes available based on the smallest and largest particle sizes available. The second design approach can be utilized to identify the preferred ratio between particles, Z, and the number of different particle sizes, n, to be utilized in the final particle blend. The extensive empirical experimental evaluations of particle size distributions generated by McGeary were then utilized to confirm the limits. [ABSTRACT FROM AUTHOR]

Nano-indentation, a depth sensing technique, is a useful and exciting tool to investigate the surface mechanical properties of a wide range of materials, particularly polymers. Knowledge of the influence of experimental conditions employed during nano-indentation on the resultant nano-mechanical response is very important for the successful design of engineering components with appropriate surface properties. In this work, nano-indentation experiments were carried out by selecting various values of frequency, amplitude, contact depth, strain rate, holding time, and peak load. The results showed a significant effect of amplitude, frequency, and strain rate on the hardness and modulus of the considered polymer, ultrahigh molecular weight polyethylene (UHMWPE). Load-displacement curves showed a shift towards the lower indentation depths along with an increase in peak load by increasing the indentation amplitude or strain rate. The results also revealed the strong dependence of hardness and modulus on the holding time. The experimental data of creep depth as a function of holding time was successfully fitted with a logarithmic creep model (R2 ≥ 0.98). In order to remove the creeping effect and the nose problem, recommended holding times were proposed for the investigated polymer as a function of different applied loads. [ABSTRACT FROM AUTHOR]

Modified soybean oil (MSO) is synthesized from soybean oil (SO) and sulfur, aiming to reduce the double bond quantity of SO and avoid harmful effects on the crosslink density and mechanical properties of rubber. MSO modified with different weight percentages of sulfur is then used to plasticize tire tread rubber (TR). It is found that the crosslink density and modulus of MSO- plasticized rubber are significantly improved compared with that of SO-plasticized TR. MSO modified with 6 wt % sulfur (MSO-6%) exhibits the best plasticization effect on TR, thus, the plasticization effect of MSO-6% on TR was further studied by adjusting its additive content. Thereafter, the Mooney viscosity, Payne effect, mechanical property of different amount of MSO-6% plasticized TR are studied to investigate their plasticization effect. At the same additive content of plasticizer, the plasticization effect of MSO-6% and a commonly used aromatic hydrocarbon plasticizer (AO) is compared to determine the potential application of MSO on tire tread rubber. It is found MSO shows similar plasticization effect on TR compared with AO. More important, the aging resistance property and wear resistance property of MSO-6% plasticized rubber are better than those of AO-plasticized rubber. Therefore, MSO-6% is a promising bio-based plasticizer for tire tread rubber. [ABSTRACT FROM AUTHOR]

This paper aims to explore the mechanisms of the complex thermo-mechanical behavior of polymer glass across a wide range of temperature variations. To this end, the free vibration frequency spectrum of simply supported poly(methyl methacrylate) (PMMA) beams was thoroughly investigated with the aid of the impulse excitation technique. It was found that the amplitude ratio of the multiple peaks in the frequency spectrum is a strongly dependent on temperature, and that the peaks correspond to the multiple vibrational modes of the molecular network of PMMA. At a low temperature, the vibration is dominated by the overall microstructure of PMMA. With increasing the temperature, however, the contribution of the sub-microstructures is retarded by β relaxation. Above 80 °C, the vibration is fully dominated by the microstructure after relaxation. The relaxation time at the transition temperature is of the same order of the vibration period, confirming the contribution of β relaxation. These findings provide a precise method for establishing reliable physical-based constitutive models of polymer glass. [ABSTRACT FROM AUTHOR]