Determination of the interfacial properties between modified soy protein resin and kenaf fiber

The kenaf fiber/soy protein resin interface was characterized. The soy protein isolate (SPI) was modified using a polycarboxylic acid, Phytagel^® (PH), to make an interpenetrating network-like (IPN-like structure) structure of the resin. The effects of different PH contents on the interfacial properties were characterized using single fiber composite (SFC) tests and optical microscopy. Kenaf fiber strength was characterized using tensile tests. Kenaf fibers were extracted from nonwoven mats. The length of each kenaf fiber was extended by gluing it to long polyethylene filaments on both sides. After drying the glue, dog-bone shaped SFC specimens were prepared using pure and modified SPI resins. The dried SFC specimens were taken out from the mold and hot-pressed (cured) at 120°C. The interfacial shear strength (IFSS) was calculated using the shear-lag analysis. Single fiber tensile tests at different gauge lengths were performed. The average stresses were computed by fitting the data to Weibull distribution. These values were used in the calculation of the IFSS. After the SFC tests, the specimens were observed under the optical microscope to characterize the fiber fracture modes and the region around the fiber fracture. The SFC tests showed that the IFSS is a function of the PH content which controls the resin shrinkage. It was also seen that the interfacial failure mode is also a function of the PH content. These finding were confirmed by the microbead tests in which E-glass fibers were used with the modified SPI resins.     

Effect of postgrafted alkyl chains on the wettability of hydrophilic poly(amidoamine)-grafted nano-sized silica

In order to control the surface wettability of hyperbranched hydrophilic poly(amidoamine) (PAMAM)-grafted nano-sized silica, hydrophilic alkyl chain (C _n H_2n+1) with different chain lengths (n = 4, 8, 15) were postgrafted onto PAMAM-grafted silica by the reaction of terminal amino groups of PAMAM grafted on the silica surface with alkyl acid chlorides (C _n H_2n+1-COCl). The postgrafting of C _n H_2n+1-COCl increased with increasing PAMAM grafting and alkyl chain length of C _n H_2n+1-COCl. However, the terminal amino groups of PAMAM-grafted silica used for the postgrafting of C _n H_2n+1-COCl decreased with increasing chain length. This may be due to the steric hindrance between terminal amino groups of PAMAM-grafted silica and C _n H_2n+1-COCl: the steric hindrance is considered to increase with increasing chain length of C _n H_2n+1-COCl. The surface wettability was estimated by contact angle measurement for water and methanol wettability. As a result, it was found that contact angle and methanol wettability increased with increasing alkyl chain length of postgrafted C _n H_2n+1-COCl. The hyperbranched PAMAM-grafted silica readily dispersed in water and methanol because of the hydrophilic nature of grafted PAMAM, but it lost dispersibility in water and methanol due to postgrafting of hydrophobic chains.     

Henequen/poly(butylene succinate) biocomposites: electron beam irradiation effects on henequen fiber and the interfacial properties of biocomposites

Henequen natural fiber-reinforced poly(butylene succinate) biocomposites were prepared through a resin microdroplet formation on a single fiber and also fabricated by a compression molding technique using chopped henequen fibers, surface-treated with electron beam irradiation (EBI) at various dosages. The effect of EBI treatment on the surface characteristics and dynamic mechanical properties of henequen fibers was investigated using SEM, XPS and DMA methods, respectively. Also, the interfacial behavior of biocomposites was explored through a single fiber microbonding test and fracture surface observations. The result indicates that the interfacial shear strength (IFSS) of biocomposites greatly depends on the EBI treatment level on the henequen fiber surface. This study also suggests that appropriate modification of natural fiber surfaces at an optimum EBI dosage significantly contributes to improving the interfacial properties of biocomposites.     

Effect of interfacial debonding and matrix cracking on mechanical properties of multidirectional composites

In composites, debonding at the fiber–matrix interface and matrix cracking due to loading or residual stresses can effect the mechanical properties. Here three different architectures — 3-directional orthogonal, 3-directional 8-harness satin weave and 4-directional in-plane multidirectional composites — are investigated and their effective properties are determined for different volume fractions using unit cell modeling with appropriate periodic boundary conditions. A cohesive zone model (CZM) has been used to simulate the interfacial debonding, and an octahedral shear stress failure criterion is used for the matrix cracking. The debonding and matrix cracking have significant effect on the mechanical properties of the composite. As strain increases, debonding increases, which produces a significant reduction in all the moduli of the composite. In the presence of residual stresses, debonding and resulting deterioration in properties occurs at much lower strains. Debonding accompanied with matrix cracking leads to further deterioration in the properties. The interfacial strength has a significant effect on debonding initiation and mechanical properties in the absence of residual stresses, whereas, in the presence of residual stresses, there is no effect on mechanical properties. A comparison of predicted results with experimental results shows that, while the tensile moduli E ₁₁, E ₃₃and shear modulus G ₁₂ match well, the predicted shear modulus G ₁₃ is much lower.     

Effect of a Novel Polymeric Coupling Agent on the Water Uptake Property and Warp Stability of Poly(vinyl chloride)/Bamboo Flour Composite

Water uptake property and warp stability of poly(vinyl chloride) (PVC)/bamboo flour composite were investigated employing a novel polymeric coupling agent, poly(styrene-co-maleic anhydride)-block-poly(styrene-co-acrylonitrile) {P[(SMA)-b-(SAN)]}. P[(SMA)-b-(SAN)] was synthesized through controlled/'living' radical polymerization (CRP) technique in an one-pot reaction and incorporated into the composite to improve the interfacial adhesion between PVC and bamboo flour. The structure of P[(SMA)-b-(SAN)] was confirmed by ¹H-NMR, FT-IR and GPC. PVC/bamboo flour composite sheets were then prepared from a single screw extruder and two-roll mill in the presence of P[(SMA)-b-(SAN)] coupling agent. As the content of the coupling agent increased, improved interfacial bonding between PVC and bamboo flour filler was observed. Water uptake property and warp stability were also improved in the presence of the coupling agent. These results suggest that the block copolymer successfully acted as a coupling agent in PVC/bamboo flour composites.     

Effect of fiber content and surface treatment on the mechanical properties of natural fiber composites produced by rotomolding

In this study, natural fibers (agave, coir, and pine) were surface treated with maleated polyethylene (MAPE) with two main objectives: (1) to improve the mechanical properties of natural fiber composites produced by rotational molding and (2) to increase the fiber content in the composite. The rotomolded composites were produced at 0, 10, 20, 30, and 40% wt. of fiber contents (treated or untreated) and characterized in terms of morphology and mechanical properties (hardness, impact, tension, and flexion). The results showed that MAPE surface treatment was more successful for agave and coir than for pine fibers due to their respective chemical composition. In general, surface treatment led to better fiber distribution and a more uniform composite morphology allowing the possibility to use higher fiber contents in rotational molding. At low fiber contents (10 and 20% wt.), the mechanical properties were improved using treated fiber composites (TFC) compared to the neat polymer and untreated fiber composites (UFC). Although the mechanical properties of TFC decreased at high fiber contents (30 and 40% wt.), they were substantially higher (about 160, 400, and 100% for impact, tensile, and flexural properties, respectively) than for UFC.     

PVDF-Based Nanocomposite Solid Polymer Electrolytes; the Effect of Affinity Between PVDF and Filler on Ionic Conductivity

Nanocomposite solid polymer electrolytes (NSPEs) based on poly(vinylidene fluoride) (PVDF) were prepared by dispersing two kinds of organoclay (Cloisite^® 30B, Cloisite^® 15A) consisting of silicate layers in the polymer matrix. The effect of affinity between PVDF and organoclay as the filler on ionic conductivity was investigated in relation to its content, dispersed condition of organoclay, and structural changes of nanocomposites. The characterizations of PVDF-based nanocomposites with various organoclay contents were carried out by XRD, TEM, DSC, and DMA. In order to confirm the ion conduction properties of NSPEs with LiCF₃SO₃ at room temperature, ac impedance analyzer and FT-IR spectrometer were used. As a result, a higher ionic conductivity appeared in the case of NSPE with C15A than that with C30B and the maximum conductivity was 1.04 × 10^–3 S/cm for the NSPE containing 5 wt% of C15A and 40 wt% of LiCF₃SO₃.     

Effect of chemical etching on the Cu/Ni metallization of poly (ether ether ketone)/carbon fiber composites

Poly(ether ether ketone)/carbon fiber composites (PEEK/Cf) were chemical etched by Cr₂O₃/H₂SO₄ solution, electroless plated with copper and then electroplated with nickel. The effects of chemical etching time and temperature on the adhesive strength between PEEK/Cf and Cu/Ni layers were studied by thermal shock method. The electrical resistance of some samples was measured. X-ray photoelectron spectroscopy (XPS) was used to analyze the surface composition and functional groups. Scanning electron microscopy (SEM) was performed to observe the surface morphology of the composite, the chemical etched sample, the plated sample and the peeled metal layer. The results indicated that CO bond increased after chemical etching. With the increasing of etching temperature and time, more and more cracks and partially exposed carbon fibers appeared at the surface of PEEK/Cf composites, and the adhesive strength increased consequently. When the composites were etched at 60 °C for 25 min and at 70-80 °C for more than 15 min, the Cu/Ni metallization layer could withstand four thermal shock cycles without bubbling, and the electrical resistivity of the metal layer of these samples increased with the increasing of etching temperature and time.     

Effect of clay silylation on curing and mechanical and thermal properties of unsaturated polyester/montmorillonite nanocomposites

This work focuses on the chemical modification of montmorillonite (MMT) (Cloisite® Na) with compatible silanes, vinyltriethoxysilane (CVTES) and γ-methacryloxypropyltrimethoxysilane (CMPS) in order to prevent agglomeration and to improve montmorillonite interaction with an unsaturated polyester resin matrix seeking to achieve a multifunctional composite. Clays were dispersed in the resin by mechanical stirring and sonication and the nanocomposites were prepared by resin transfer into a mold. The mechanical, morphological, thermal and flammability properties of the obtained composites were compared with those prepared using commercial Cloisite® 30B (C30B) and Cloisite® 15A (C15A) clays. Advantages of using silane-modified clays (CVTES and CMPS) as compared with organic-modified clays (C30B and C15A) can be summarized as similar flexural strength and linear burning rate but higher storage modulus and improved adhesion to the polyester resin with consequent higher thermal deflection temperature and reinforcement effectiveness at higher temperatures. However, organic modified clays showed better dispersion (tendency to exfoliate) and consequently delayed thermal volatilization due to the clay barrier effect.     

Effect of [Zn]/[S] ratios on the properties of chemical bath deposited zinc sulfide thin films

ZnS thin films have been prepared by chemical bath deposition (CBD) technique onto glass substrates deposited at about 80 °C using aqueous solution of zinc sulfate hepta-hydrate, ammonium sulfate, thiourea, ammonia and hydrazine hydrate. Ammonia and hydrazine hydrate were used as complexing agents. The influence of the ratio of [Zn]/[S] on formation and properties of ZnS thin films has been investigated. The ratio of [Zn]/[S] was changed from 3:1 to 1:9 by varying volumes and/or concentrations of zinc sulfate hepta-hydrate and thiourea in the deposition solution. The structural and morphological characteristics of films have been investigated by X-ray diffraction (XRD), scanning electron microscope and UV-vis spectroscopic analysis. ZnS films were obtained with the [Zn]/[S] ratio ranged from1:1 to 1:6. In the cases of [Zn]/[S] ratio ≥ 3:1 or ≤1:9, no deposition was found. Transparent and polycrystalline ZnS film was obtained with pure-wurtzite structure at the [S]/[Zn] ratio of 1:6. The related formation mechanisms of CBD ZnS are discussed. The deposited ZnS films show good optical transmission (80-90%) in the visible region and the band gap is found to be in the range of 3.65-3.74 eV. The result is useful to further develop the CBD ZnS technology.     

Effect of arc spraying power on the microstructure and mechanical properties of Zn-Al coating deposited onto carbon fiber reinforced epoxy composites

This paper investigates the effect of arc spraying power on the microstructure and mechanical properties of Zn-Al coatings deposited on carbon fiber reinforced epoxy composites (CFRE composites). The bond strength between the Zn-Al coatings and the substrates was tested on a RGD-5 tensile testing machine. The microstructures and phase composition of the as-sprayed coatings were examined by scanning electron microscopy (SEM) and X-ray diffraction (XRD), respectively. The results showed that both the melting extent of Zn-Al particles and the bond strength of the coatings were evidently improved by increasing the spraying power. Moreover, the content of crystalline Zn-Al coatings was slightly changed. Observation of fracture surfaces showed that the Zn-Al coatings could bond well with the carbon fiber bundles using 40 kW spraying power.     

Deformation-induced martensite and nanotwins by cryogenic laser shock peening of AISI 304 stainless steel and the effects on mechanical properties

Laser shock peening (LSP) of stainless steel 304 was carried out at room and cryogenic temperature (liquid nitrogen temperature). It was found that the deformation-induced martensite was generated by LSP only when the laser-generated plasma pressure is sufficiently high. Compared to room temperature laser shock peening (RT-LSP), cryogenic laser shock peening (CLSP) generates a higher volume fraction of martensite at the same laser intensity. This is due to the increase in the density of potential embryos (deformation bands) for martensite nucleation by deformation at cryogenic temperature. In addition, CLSP generates a high density of deformation twins and stacking faults. After CLSP, an innovative microstructure, characterised by networks of deformation twins, stacking faults and composite structure (martensite and austenite phases), contributes to material strength and microstructure stability improvement. The combined effect of higher surface hardness and a more stabilised microstructure results in greater fatigue performance improvement of the CLSP samples compared to that of the RT-LSP samples.     

Effect of Nafion dispersion solvent on the interfacial properties between the membrane and the electrode of a polymer electrolyte membrane-based fuel cell

A new Nafion binder solution was prepared using a different organic solvent, dimethylacetamide (DMAc), and applied to a polymer electrolyte membrane-based fuel cell. Wide angle X-ray diffraction (WAXD), electrochemical impedance spectroscopy (EIS), and polarization of the fuel cell were carried out to determine the crystallinity of the Nafion binder film, the cell resistance, and the fuel cell performance. This new Nafion binder film, which was created using a homemade Nafion solution containing DMAc, dissolved slower than a recast Nafion film that was made using a commercial Nafion solution in methanol (2 M). It was found that the slow dissolution of the homemade Nafion binder film was due to a more highly developed crystalline morphology, which can lead to good structural integrity in the catalyst layer for long-term operation of the fuel cell. The micellar structure of Nafion in the commercial Nafion binder solution is broken by new organic solvent, which leads to higher physical chain entanglement between the Nafion membrane and the Nafion binder during preparation of the membrane/electrode assembly (MEA), thereby improving the interfacial stability between the membrane and the electrode and providing long-term stability of the fuel cell.     

Thermodynamic approach to enhance the dispersion of graphene in epoxy matrix and its effect on mechanical and thermal properties of epoxy nanocomposites

Graphene-reinforced polymer nanocomposites are under intense investigation in recent years. In this work, graphene nanosheets have been prepared using chemical reduction method of graphene oxide. Graphene-reinforced epoxy nanocomposites show an enhancement in mechanical and thermal properties at 0.05 wt.% of graphene in epoxy matrix. Modification of graphene with polyvinylpyrrolidone (PVP) shows the significant enhancement in mechanical and thermal properties of epoxy nanocomposites. PVP-modified graphene nanosheets reduces the gap of enthalpic and entropic penalties and facilitates improved dispersion of graphene in epoxy matrix. In addition, enhanced dispersion of PVP-modified graphene in epoxy matrix results in better load transfer across graphene–epoxy interface. Glass transition temperature (T_g) of PVP-modified graphene epoxy nanocomposites increases as compared to pure epoxy because there exist an interaction between epoxy and PVP. Fractography study reveals the localized ductile fracture.     

Effect of the shell on the transport properties of poly(glycerol) and Poly(ethylene imine) nanoparticles

Dendritic core–shell architectures containing poly (glycerol) and poly (ethylene imine) cores and poly(lactide) shell (PG-PLA and PEI-PLA respectively) were synthesized. Analogous of these core–shell architectures containing the same cores but poly (L-lactide) shell (PG-PLLA and PEI-PLLA, respectively) were also synthesized. In this work PG and PEI were used as macroinitiator for ring opening polymerization of the lactid and L-lactide monomers. Different molar ratios of monomer to end functional groups of PG ([LA]/[OH]) and PEI ([LA]/[NHn] (n = 1 or 2)) were used to prepare the core–shell architectures with different shell thickness. These core–shell architectures were able to encapsulate and transport the small guest molecules. Their transport capacity (TC) depended on the type and thickness of the shells. TC of core–shell architectures containing PLLA shell was higher than that for their analogs containing PLA shell. The diameter of core–shell architectures was between 20–80 nm. The rate of release of guest molecules from chloroform solution of nanocarriers to water phase was investigated and it depended on the type of the core, shell and solvent.     

Effects of the ultrasonic flexural vibration on the interaction between the abrasive particles; pad and sapphire substrate during chemical mechanical polishing (CMP)

In this paper, the technique of ultrasonic flexural vibration assisted chemical mechanical polishing (UFV-CMP) was used for sapphire substrate CMP. The functions of the polishing pad, the silica abrasive particles, and the chemical additives of the slurry such as pH value regulator and dispersant during the sapphire's UFV-CMP were investigated. The results showed that the actions of the ultrasonic and silica abrasive particles were the main factors in the sapphire material removal rate (MMR) and the chemical additives were helpful to decrease the roughness of sapphire. Then the effects of the flexural vibration on the interaction between the silica abrasive particles, pad and sapphire substrate from the kinematics and dynamics were investigated to explain why the MRR of UFV-CMP was bigger than that of the traditional CMP. It indicated that such functions improved the sapphire's MRR: the increasing of the contact silica particles’ motion path lengths on the sapphire's surface, the enhancement of the contact force between the contact silica particles and the sapphire's surface, and the impaction of the suspending silica particles to the sapphire's surface.     

Effect of vapors of the simplest alcohols on the structure and properties of YBa2Cu3Oy compounds

With low-temperature treatments (200–300°C), the effect of alcohol vapors on the structural and electrophysical properties of YBa₂Cu₃O_y (123) having different oxygen content has been studied. It has been established that CuO and YBa₂Cu₃O_y are catalysts for the dehydration of alcohols to form water and aldehydes. Similar to the action of water vapors, the treatment in vapors of the simplest alcohols leads to hydration of 123 and its transformation into the pseudo-124 phase. In this case, planar stacking faults are formed to be centres of pinning and can improve the critical characteristics of high-temperature superconductors (HTSС) in magnetic fields. The influence of the alcohol vapors is more ‘mild’ as compared to the treatment in water vapors. At t?=?300°C, the alcohols are reducing agents of copper, followed by the decomposition of 123 into simple compounds.     

Effect of ultrasonic irradiation on the properties and performance of biodiesel produced from date seed oil used in the diesel engine

In the present study, the effect of ultrasound irradiation on the transesterification parameters, biodiesel properties, and its combustion profiles in the diesel engine was investigated. Moreover, date seed oil (DSO) was firstly utilized in the ultrasound-assisted transesterification reaction. DSO was extracted from Zahidi type date (Phoenix dactylifera) and was esterified to reduce its Free Fatty Acid (FFA) content. Biodiesel yield was optimized in both heating methods, so that the yield of 96.4% (containing 93.5% ester) at 60 °C, with 6 M ratio of methanol/oil, 1 wt% of catalyst (NaOH) and at 90 min of reaction time was reported. The ultrasound irradiation did not influence the reaction conditions except reaction time, reduced to 5 min (96.9% yield and 91.9% ester). The ultrasonic irradiation also influenced on the physicochemical properties of DSO biodiesel and improved its combustion in the diesel engine. The analysis results related to the engine and gas emission confirmed that the ultrasound-assisted produced biodiesel has lower density and viscosity, and higher oxygen content facilitating injection of fuel in the engine chamber and its combustion, respectively. Although, B40 (biodiesel blend consisting of 40% biodiesel and 60% net diesel fuel) as a blend of both fuels presented higher CO₂ and lower CO and HC in the emissions, the DSO biodiesel produced by ultrasound irradiation presented better specifications (caused about 2-fold improvement in emissions than that of conventional method). The findings of the study confirmed the positive effect of the ultrasound irradiation on the properties of the produced biodiesel along with its combustion properties in the diesel engine, consequently reducing air pollution problems.     

Effect of disaccharide,gamma radiation and temperature on the physico-mechanical properties of jute fabrics reinforced unsaturated polyester resin-based composite

The jute fabrics reinforced unsaturated polyester resin (jute/UPR)-based composites were prepared successfully by the hand-lay-up technique. The percentage of jute fabrics was kept constant at 40% fiber (by weight). The disaccharide percentage was also kept constant at 2% (by weight), but at this percentage the mechanical properties were lower than the untreated composites. Gamma radiation dose was varied at 0, 2.5, 5 and 7.5?kGy for jute/UPR-based composites. At 5.0?kGy gamma dose highest TS, TM and Eb were obtained. The jute/UPR-based composites were treated under 30°C, 50°C and ?18°C for the measurement of mechanical properties. At low temperature (?18°C), the highest mechanical properties were observed. The water uptake properties were measured for disaccharide-treated and disaccharide-untreated composites up to 10 days, but no water was absorbed by the composites. The soil degradation test was carried out under 12 inch soil containing at least 25% water, but no significant decrease was observed for untreated and sucrose-treated composites. For the functional group analysis, FT-IR was carried out. For the fiber matrix adhesion analysis, the scanning electron microscopic image was taken.     

Effect of heat treatment on the optical and electrical transport properties of Ge15Sb10Se75 and Ge25Sb10Se65 thin films

The effect of heat treatment on the optical and electrical properties of Ge₁₅Sb₁₀Se₇₅ and Ge₂₅Sb₁₀Se₆₅ thin films in the range of annealing temperature 373-723 K has been investigated. Analysis of the optical absorption data indicates that Tauc's relation for the allowed non-direct transition successfully describes the optical processes in these films. The optical band gap (E_g^opt.) as well as the activation energy for the electrical conduction (ΔE) increase with the increase of annealing temperature (T_a) up to the glass transition temperature (T_g). Then a remarkable decrease in both the E_g^opt. and ΔE values occurred with a further increase of the annealing temperature (T_a>T_g). The obtained results were explained in terms of the Mott and Davis model for amorphous materials and amorphous to crystalline structure transformations. Furthermore, the deduced value of E_g^opt. for the Ge₂₅Sb₁₀Se₆₅ thin film is higher than that observed for the Ge₁₅Sb₁₀Se₇₅ thin film. This behavior was discussed on the basis of the chemical ordered network model (CONM) and the average value for the overall mean bond energy 〈E〉 of the amorphous system Ge_xSb₁₀Se_90−x with x=15 and 25 at%. The annealing process at T_a>T_g results in the formation of some crystalline phases GeSe, GeSe₂ and Sb₂Se₃ as revealed in XRD patterns, which confirms our discussion of the obtained results.