Microfiber SMPU film affords quicker shape recovery than the bulk one

Comparing to the bulk SMPU (shape memory polyurethane) film, microfiber SMPU film afforded much quicker and sharper shape recovery when heated in water bath. The shape recovery of the microfiber film only took ~ 1/4 time of that needed for the bulk film from R_r (shape recovery ratio) = 10% to R_r = 90%. The final R_r and R_f (shape fix ratio) of the microfiber film was also enhanced. The microfiber film was fabricated by electrospinning with the fiber diameter of 200 nm to 1 μm. DSC and DMA results indicate that the formation of microfiber has very limited effect on the T_trans (switching temperature) of the SMPU. The quick shape recovery of the microfiber SMPU film is considered due to the higher surface area of microfiber film that is favorable for quicker heating/cooling of the sample and quicker diffusion of water. This study offers a possible way to improve the shape recovery speed without changing the chemical composition, which may meet special needs for sensors or actuators of biomedical devices and others.     

Effect of carbonization temperature on properties of aligned electrospun polyacrylonitrile carbon nanofibers

Aligned electrospun nanofibrous bundle was used as the raw material for pretreatment, preoxidation and carbonization processes to prepare carbon nanofibers in a procedure temperature-controlled sintering furnace. Effect of carbonization temperature on the morphology and structural performance of nanofibers was investigated in present study. Results showed that R_I (the relative intensity radio between Disordered peak and Graphite peak) of nanofibers carbonized at 1000 °C is 0.90, carbon content is up to 85.67%, conductivity is 105.44 S·cm^− 1, Young's modulus is 68.8 ± 0.42 GPa, and fiber strength is 306.0 ± 9.0 MPa, all of which endow the fibers with a superior comprehensive property.     

Xylan polysaccharides fabricated into nanofibrous substrate for myocardial infarction

Myocardial infarction, a main cause of heart failure, leads to loss of cardiac tissue impairment of left ventricular function. Repair of diseased myocardium with in vitro engineered cardiac muscle patch/injectable biopolymers with cells may become a viable option for myocardial infarction. We attempted to solve these problems by in vitro study by selecting a plant based polysaccharides beech wood Xylan for the normal functioning of infarcted myocardium. The present study fabricated Xylan based nanofibrous scaffolds cross-linked with glutaraldehyde (Glu) vapors for 24 h, 48 h and 1% Glu blended fibers for the culture of neonatal rat cardiac cells for myocardial infarction. These nanofibers were characterized by SEM, FT-IR, tensile testing and cell culture studies for the normal expression of cardiac proteins. The observed results showed that the Xylan/polyvinyl alcohol (PVA) 24 h Glu vapor cross-linked nanofibers (427 nm) having mechanical strength of 2.43 MPa and Young modulus of 3.74 MPa are suitable for the culture of cardiac cells. Cardiac cells proliferation increased only by 11% in Xylan/PVA 24 h Glu cross-linked nanofibers compared to control tissue culture plate (TCP). The normal cardiac cell morphology was observed in 24 h cross-linked Xylan/PVA nanofibers but 48 h cross-linked fibers cell morphology was changed to flattened and elongated on the fibrous surfaces. Confocal analysis for cardiac expression proteins actinin, connexin 43 was observed normally in 24 h Glu cross-linked nanofibers compared to all other nanofibrous scaffolds. The fabricated Xylan/PVA nanofibrous scaffold may have good potential for the normal functioning of infarcted myocardium.     

Fabrication and evaluation of polyamide 6 composites with electrospun polyimide nanofibers as skeletal framework

In this study, two types of polyimide (PI) nanofiber mats, including (1) the mats consisting of (almost) randomly overlaid PI nanofibers and (2) the mats consisting of highly aligned PI nanofibers, were prepared by the materials-processing technique of electrospinning. The nanofiber mats were subsequently used to develop composites with polyamide 6 (PA6) via the composites – fabrication method of polymer melt infiltration lamination (PMIL). Owing to superior mechanical properties (i.e., the tensile strength and modulus were 1.7 GPa and 37.0 GPa, respectively) and large specific surface area of electrospun PI nanofibers, the PI/PA6 composites with PI nanofiber mats as skeletal framework demonstrated excellent mechanical properties. In particular, the PI/PA6 composite containing 50 wt.% of aligned PI nanofibers had the tensile strength and modulus of 447 MPa and 3.0 GPa along the longitudinal direction, representing ～700% and ～500% improvements as compared to neat PA6.     

Magnetically-sensitive shape memory polyurethane composites crosslinked with multi-walled carbon nanotubes

Magnetically-sensitive polyurethane composites, which were crosslinked with multi-walled carbon nanotubes (MWCNTs) and were filled with Fe₃O₄ nanoparticles, were synthesized via in situ polymerization method. MWCNTs pretreated with nitric acid were used as crosslinking agents. Because of the crosslinking of MWCNTs with polyurethane prepolymer, the properties of the composites with a high content of Fe₃O₄ nanoparticles, especially the mechanical properties, were significantly improved. The composites showed excellent shape memory properties in both 45 °C hot water and an alternating magnetic field (f = 45 kHz, H = 29.7 kA m⁻¹). The shape recovery time was less than one minute and the shape recovery rate was over 95% in the alternating magnetic field.     

Martensitic transformation behaviors of rapidly solidified Ti–Ni–Mo powders

For the fabrication of bulk near-net-shape shape memory alloys and porous metallic biomaterials, consolidation of Ti–Ni–Mo alloy powders is more useful than that of elemental powders of Ti, Ni and Mo. Ti₅₀Ni_49.9Mo_0.1 shape memory alloy powders were prepared by gas atomization, and transformation temperatures and microstructures of those powders were investigated as a function of powder size. XRD analysis showed that the B2–R–B19 martensitic transformation occurred in powders smaller than 150 μm. According to DSC analysis of the as-atomized powders, the B2–R transformation temperature (T_R) of the 25–50 μm powders was 18.4 °C. The T_R decreased with increasing powder size, however, the difference in T_R between 25–50 μm powders and 100–150 μm powders is only 1 °C. Evaluation of powder microstructures was based on SEM examination of the surface and the polished and etched powder cross sections and the typical images of the rapidly solidified powders showed cellular morphology. Porous cylindrical foams of 10 mm diameter and 1.5 mm length were fabricated by spark plasma sintering (SPS) at 800 °C and 5 MPa. Finally these porous TiNi alloy samples are heat-treated for 1 h at 850 °C, and then quenched in ice water. The bulk samples have 23% porosity and 4.6 g/cm³ density and their T_R is 17.8 °C.     

Study of the thermal properties of shape memory polyurethane nanofibrous nonwoven

Thermal properties of polymer are very important to the understanding of morphology and shape memory effect of shape memory polymers (SMPs). In this article, the thermal properties of shape memory polyurethane nanofibrous nonwoven are investigated systematically from the morphology of nanofibers, crystalline structure, isothermal crystallization behavior, and thermal-dependent strain recovery. The results indicate that the thermal properties of shape memory polyurethane nanofibrous nonwoven are influenced greatly by the electro-spinning and the recrystalline condition. The crystal melting temperature (T _m) decreases as the crystallization temperature (T _c) decreases, while the relative degree of crystallinity (X _c) increases with the decrease of T _c within the temperature range of 20 to −30 °C. In particular, when the annealing temperature is higher than 150 °C, the T _m shifts to higher value and the X _c decreases significantly with the increase of T _c. Finally, temperature-dependent strain recovery curves show that the shape memory polyurethane nanofiber tends to have a lower recovery temperature as compared with the SMPU bulk film due to their ultrafine diameter.     

Preparation and properties of biomimetic porous nanofibrous poly(l-lactide) scaffold with chitosan nanofiber network by a dual thermally induced phase separation technique

A biomimetic nanofibrous poly(l-lactide) scaffold decorated by chitosan nanofiber network inside the macropores was fabricated using a dual thermally induced phase separation technique. The first phase separation was used to build a nanofibrous poly(l-lactide) scaffold with interconnected macropores, where chitosan nanofibers about 500 nm in diameter were incorporated via the second phase separation. The content of nanofibrous chitosan was determined to be 5.76 in weight percentage by elemental analysis. The composite scaffold showed the highest protein adsorption of 7225 ± 116 μg/cm³ and the most hydroxyapatite crystal deposition in the mineralization. Compared with non-nanofibrous poly(l-lactide) scaffold, nanofibrous poly(l-lactide) scaffold exhibited a much faster degradation, but it could be restrained by the introduced chitosan nanofibers. The bone mesenchymal stem cell culture results indicated that the cells would rather attach and stretch along the chitosan nanofibers in the composite scaffold that showed the highest viability and the best cytocompatibility may be attributed to the biomimetic nanofibrous network and good cell affinity of chitosan nanofibers.     

Enhanced thermal conductivity of SiCp/PS composites by electrospinning–hot press technique

Silicon carbide particle/polystyrene (SiCp/PS) electrospun mats are firstly prepared by electrospinning technology, then to be fabricated the corresponding thermally conductive SiCp/PS composites by the method of “laminating-hot press”. The mass fraction of SiCp and laminating mode of SiCp/PS electrospun mats affecting on the thermal conductivities, dielectric and thermal properties of the composites are investigated. The addition of 32.8 vol% SiCp improves the thermally conductive coefficient λ of pure PS from 0.182 to 0.566 W/m K and thermal diffusivity of pure PS from 0.169 to 0.376 mm²/s, whereas the dielectric constant values still remain at relatively low levels. The thermal stabilities of the SiCp/PS composites are increased with the increasing addition of SiCp. For a given SiCp loading, the SiCp/PS composites from warp–weft arrangement of SiCp/PS electrospun mats possess relative higher thermally conductive coefficient λ and dielectric constant values than those of SiCp/PS composites from warp–warp arrangement of SiCp/PS electrospun mats.     

Gold nanoparticle/polymer nanofibrous composites by laser ablation and electrospinning

Poly(vinylpyrolidone) (PVP) nanofibers incorporating gold nanoparticles (Au-NPs) were produced in combination with laser ablation and electrospinning techniques. The Au-NPs were directly synthesized in PVP solution by laser ablation and then, the electrospinning of PVP/Au-NPs solution was carried out for obtaining nanofibrous composites. The presence of Au-NPs in the PVP nanofibers was confirmed by SEM, TEM and EDX analyses. The SEM imaging elucidated that the electrospun PVP/Au-NPs nanofibers were bead-free having average fiber diameter of 810 ± 480 nm. The TEM imaging indicated that the Au-NPs were in spherical shape having diameters in the range of 5 to 20 nm and the Au-NPs were more or less dispersed homogeneously in the PVP nanofiber matrix. The FTIR study suggested the presence of molecular interactions between PVP matrix and the Au-NPs in the nanofibrous composites. The UV–Vis measurement confirmed the enhancement of the optical properties of the PVP/Au-NPs nanofibers in the solid state due to the surface plasma resonance effect of Au-NPs.     

A facile assembly of polyimide/graphene core–shell structured nanocomposites with both high electrical and thermal conductivities

Polyimide/reduced graphene oxide (PI/r-GO) core–shell structured microspheres were fabricated by in-situ reduction of graphene oxide (GO), which was coated on the surface of PI microspheres via hydrogen bonding and π–π stacking interaction. The highly ordered 3D core–shell structure of PI/r-GO microspheres with graphene shell thickness of 3 nm was well characterized by scanning electron microscope (SEM), transmission electron microscopy (TEM) and Raman spectra. The glass transition temperature (T_g) of PI/r-GO microspheres was slightly increased because of the interaction of r-GO and PI matrix while the temperature at 5% weight loss (T_5%) of PI/r-GO microspheres was decreased due to the side effect of reductant hydrazine hydrate. The PI/r-GO nanocomposites exhibited highly electrical conductivity with percolation threshold of 0.15 vol% and ultimate conductivity of 1.4 × 10⁻² S/m. Besides, the thermal conductivity of PI/r-GO nanocomposites with 2% weight content of r-GO could reach up to 0.26 W/m K.     

Ni24.7Ti50.3Pd25.0 high temperature shape memory alloy with narrow thermal hysteresis and high thermal stability

High temperature shape memory alloys with operating temperatures above 100 °C are in demand for use as solid-state thermal actuators in aerospace, automobile and other engineering applications. The present study deals with transformation behaviour and thermal stability of Ni_24.7Ti_50.3Pd_25.0 (at.%) high temperature shape memory alloy, in cast and homogenized condition. The martensite finish temperature and transformation hysteresis of the alloy were determined to be 181.0 °C and ∼8.5 °C respectively. The alloy showed high stability upon stress-free thermal cycling, variation in transformation temperatures being ±1 °C. The narrow thermal hysteresis and high thermal stability of the alloy upon transformation cycling has been discussed and correlated with its microstructural features, activation energy and elastic strain energy of thermoelastic martensitic transformation. The alloy exhibited modulus of ∼82 GPa and hardness of ∼4.7 GPa in martensite phase.     

Influence of defects on fatigue strength and failure mechanisms in the VHCF-region for quenched and tempered steel and nodular cast iron

Investigations are presented in this paper on quenched and tempered steel 42CrMoS4 from two batches, with two different tensile strengths (R_m = 1100 MPa, 1350 MPa) but with similar microstructure, and a nodular cast iron EN-GJS-900-2 (R_m = 930 MPa). Fatigue tests with smooth (K_t = 1) and notched (K_t = 1.75) specimens were performed at R = −1 and R = 0 up to the number of cycles N = 2·10⁹ in order to determine the fatigue strength behaviour and failure mechanisms, especially in the VHCF-region. Failure in smooth specimens often initiated at material defects such as oxides in the quenched and tempered steel and shrinkage holes in the nodular cast iron. Firstly, a fatigue strength analysis was performed that did not consider these defects. A possibility of analysis of experimental data including VHCF-results has been discussed. Next, a linear elastic fracture mechanics analysis was performed in order to describe the defect behaviour, assuming that the defects act like cracks. The results showed that there are lower limit or threshold values of the stress intensity factor range ΔK for crack propagation in both materials. Analysis of defects and defect distribution in run-out specimens confirmed this conclusion. From the comparison of the results with an S–N curve from the design code FKM-Guideline Analytical strength assessment of components, recommendations for design and assessment of components have been derived.     

Enhanced thermal conductivity and dielectric properties of Al/β-SiCw/PVDF composites

Polymeric composites with high thermal conductivity, high dielectric permittivity but low dissipation factor have wide important applications in electronic and electrical industry. In this study, three phases composites consisting of poly(vinylidene fluoride) (PVDF), Al nanoparticles and β-silicon carbide whiskers (β-SiC_w) were prepared. The thermal conductivity, morphological and dielectric properties of the composites were investigated. The results indicate that the addition of 12 vol% β-SiC_w not only improves the thermal conductivity of Al/PVDF from 1.57 to 2.1 W/m K, but also remarkably increases the dielectric constant from 46 to 330 at 100 Hz, whereas the dielectric loss of the composites still remain at relatively low levels similar to that of Al/PVDF at a wider frequency range from 10⁻¹ Hz to 10⁷ Hz. With further increasing the β-SiC_w loading to 20 vol%, the thermal conductivity and dielectric constant of the composites continue to increase, whereas both the dielectric loss and conductivity also rise rapidly.     

Research on the microstructure,fatigue and corrosion behavior of permanent mold and die cast aluminum alloy

Permanent mold (PM) and high pressure die cast (HPDC) AlMg5Si2Mn are employed to investigate the microstructure, fatigue strength and corrosion resistance. Results indicated that the mechanical properties (R_m, R_0.2 and δ) of HPDC specimens (314 MPa, 189 MPa and 7.3%) are significantly better than those of PM specimens (160 MPa, 111 MPa and 2.5%) due to the finer grain size and less cast defects. Fatigue cracks of PM samples dominantly initiated from shrinkage pores and obscure fatigue striations are observed in crack growth region. Corrosion and pitting potentials of PM and HPDC AlMg5Si2Mn alloy are around −1250 mV, −760 mV and −1220 mV, −690 mV respectively. Numerous pits are observed around the grain boundaries because the corrosion potential of Mg₂Si is more anodic than that of α-Al matrix. In addition, the superior corrosion resistance of HPDC samples can be attributed to the fine grain size and the high boundary density which improved the formation of oxide layer on the surface and prevented further corrosion.     

Multi-step microwave reduction of graphite oxide and its use in the formation of electrically conductive graphene/epoxy composites

The multi-step MW reduction technique was developed in this study to obtain reduced graphene oxides; EG, RGO-1, and RGO-2 with MW irradiation time of 1, 2, and 3 min, respectively. Results of TGA, IR, and elemental analysis demonstrated that the degree of reduction of GO increased with increasing the MW irradiation time. Overall, 3 min of MW irradiation of GO in 3 steps was sufficient to obtain highly reduced GO (C/O ratio 10.38 by elemental analysis). The electrical percolation threshold of composites was observed as 1 wt% and 0.3 wt% for RGO-1 and RGO-2, respectively. Even at 0.5 wt% loading of RGO-2 in epoxy, the T_g value of the composite increased by 10 °C, indicating a strong interfacial interaction between graphene and epoxy resin.     

Effect of Fe and Co doping on electrical and thermal properties of La0.5Ce0.5Mn1−x(Fe,Co)xO3 manganites

The effect of Fe and Co doping on structural, electrical and thermal properties of half doped La_0.5Ce_0.5Mn_1−x(Fe, Co)_xO₃ is investigated. The structure of these crystallizes in to orthorhombically distorted perovskite structure. The electrical resistivity of La_0.5Ce_0.5MnO₃ exhibits metal-semiconductor transition (T_MS at ∼225 K). However, La_0.5Ce_0.5Mn_1−xTM_xO₃ (TM = Fe, Co; 0.0 ≤ x ≤ 0.1) manganites show semiconducting behavior. The thermopower measurements infer hole as charge carriers and electron–magnon as well spin wave fluctuation mechanism are effective at low temperature domain and SPC model fits the observed data at high temperature. The magnetic susceptibility measurement confirms a transition from paramagnetic to ferromagnetic phase. The observed peaks in the specific heat measurements, shifts to lower temperatures and becomes progressively broader with doping of transition metals on Mn-site. The thermal conductivity is measured in the temperature range of 10–350 K with a magnitude in between 10 and 80 mW/cm K.     

Crystal growth,structure, infrared spectroscopy,and luminescent properties of rare-earth gallium borates RGa3(BO3)4, R = Nd,Sm–Er,Y

Crystals of the rare-earth gallium borates RGa₃(BO₃)₄, where R = Nd, Sm–Er, or Y, were grown by the flux method. The crystal structures of RGa₃(BO₃)₄ (R = Eu, Ho) were studied on the basis of single-crystal X-ray diffraction measurements. The hexagonal unit-cell parameters are a = 9.4657(1) Å, c = 7.4667(1) Å and a = 9.4394(2) Å, c = 7.4322(1) Å for EuGa₃(BO₃)₄ and HoGa₃(BO₃)₄, respectively, space group R32. Structure model was determined by “charge flipping” method and refined to R = 1.93% [EuGa₃(BO₃)₄] and R = 1.89% [HoGa₃(BO₃)₄] in anisotropic approximation. All grown gallium borates were investigated by infrared (IR) spectroscopy technique in a middle and far IR region. IR spectra of rare-earth gallium borates correspond to a pure rhombohedral (R32) polytype structure. Small inclusions of a monoclinic phase were detected only in Eu and Nd compounds. Luminescence of Eu and Ho gallium borates was studied at room temperature. The measured decay times for the most intensive emission lines of EuGa₃(BO₃)₄ (∼614 nm) and HoGa₃(BO₃)₄ (434 nm) are 940 μs and 140 μs, respectively. The scheme of crystal-field energy levels of Eu³⁺ in EuGa₃(BO₃)₄ was built on the basis of the temperature-dependent optical transmission measurements combined with the luminescence data. The measured UV absorption edge for RGa₃(BO₃)₄ is at about 300 nm.     

Deposition and characterization of ultra-high barrier coatings for flexible electronic applications

A barrier structure consisting of SiO_x and SiN_x films was deposited on the polymer substrate at 80 °C via plasma-enhanced chemical vapor deposition (PECVD). However, the low radius of curvature (R_c) of the barrier-coated substrate may cause the inconvenience of the following fabrication processes. By depositing a 150 nm-SiN_x film, the R_c of the barrier-coated polycarbonate (PC) substrate can increase from 80 to 115 mm without inducing any cracks in the barrier structure. Furthermore, the thermal stress of the barrier structure can be adjusted via extending the PECVD process duration in the chamber and replacing PC by the polyethersulone (PES) substrate. The R_c can increase to ∼356 mm by depositing the 150 nm-SiN_x film on the other side of the PES substrate. Finally, the calcium test result of the barrier films/PES/SiN_x sample was calculated to be around 3.05 × 10⁻⁶ g/m²/day, representing that the barrier structure did not fail after modification.     

Effect of polymer modifier chain length on thermal conductive property of polyamide 6/graphene nanocomposites

The influence of polymer modifier chain length on the thermal conductivity of polyamide 6/graphene (GA) nanocomposites, including through-plane (λ_z) and in-plane (λ_x) directions were investigated. Here, three chain lengths of double amino-terminated polyethylene glycol (NH₂–PEG–NH₂) were used to covalently functionalize graphene with graphene content of 5.0 wt%. Results showed that λ_z was enhanced with the chain length of NH₂–PEG–NH₂ increased, but λ_x reached a maximum value at a certain chain length of NH₂–PEG–NH₂. The maximum λ_z and λ_x of GA are 0.406 W m⁻¹ K⁻¹ and 9.710 W m⁻¹ K⁻¹, respectively. This study serves as a foundation for further research on the thermal conductive property of graphene nanocomposites using different chain lengths of polymer modifier to improve the λ_z and λ_x of the thermal conductive materials.