Effect of γ-radiation on the structure and mechanical properties of polycaproamide fibres

Not only the tensile characteristics but also the character of the P(ε) and ε(T)curves change in γ-irradiation of PCA fibres. Irradiation in a forevacuum causes fewer changes in the structure and mechanical properties of PCA fibres than irradiation in air. In irradiation of PCA fibres in air, a shrinkage stage is detected, replaced by a stage of spontaneous lengthening as the absorbed dose increases. In the case of irradiation in a forevacuum (in the dose range studied), only the shrinkage stage is observed. The shrinkage stage is characterized by slight disordering of the structure of the polymer and an increase in the angle of disorientation of crystallites. Recrystallization processes activated by the radiation and to a great degree due to an increase in the molecular mobility because of fragmentation of transfer chains take place in the spontaneous lengthening stage. Translated from Khimicheskie Volokna, No. 2, pp. 47–50, March–April, 1998.     

Effect of γ-radiation on the electrical conductivity of polycaproamide fibres

The electrical conductivity of polycaproamide fibres decreases by more than 100 times in the γ-radiation dose range of 0≤D≤1.6 MGy. The change in the conductivity of irradiated PCA fibres is unambiguously correlated with a change in their structure, strength, and thermomechanical properties. Rupture of chemical bonds in the polymer chain is the basic process in γ-irradiation of PCA fibres in air. St. Petersburg State University of Technology and Design. Translated fromKhimicheskie Volokna, No. 3, pp. 40–41, May–June, 1999.     

The effect of γ-radiation on the mechanical properties of structural adhesive

The modular satellite concept iBOSS (intelligent Building Blocks for On-Orbit Satellite Servicing and Assembly) enables on-orbit servicing and reconfiguration of satellite systems and has the potential to be a game changer in the space industry. Such building blocks have to withstand all environmental loads in space, e.g.: radiation, vacuum and thermal cycling.The present paper investigates the mechanical properties of the two component epoxy adhesive 3M SW9323 under the environmental effect of radiation. This adhesive is part of the building block's primary structure. Furthermore, adhesive bonding is the sole joining technique used in the whole structure. It is therefore critical to know the influence of ionizing radiation on its load-carrying capacity. For this purpose bulk specimens were manufactured and exposed to γ-radiation, generated by a ⁶⁰Co source. Four different doses were achieved by varying the distance to the source and irradiation time. Afterwards the specimen were tested under tensile loading. Using the digital image correlation technique properties like elastic modulus, shear modulus, tensile strength and elongation at break were determined.The results show that the mechanical properties of the bulk specimen of 3M SW9323 are not influenced by γ-radiation up to a dose of 17.6 kGy. This is explained by the phenomena of crosslinking and chain scission which occur simultaneously and cancel each other out. In addition, Fourier-transform infrared spectroscopy (FTIR) was carried out to investigate if one mechanism is predominant. A slight shift in the spectra indicates the supremacy of chain scission.     

Studies on the effects of γ-radiation on the mechanical properties of Nylon 6–12 fibers

Summary Commercial nylon 6–12 fibers were subjected to various doses of -radiation. The mechanical and some thermal properties, as compared to those of non-irradiated fibers, show changes which are discussed in terms of the radiation-matter interactions.     

Effect of annealing temperature on structural and optoelectronic properties of γ-CuI thin films prepared by the thermal evaporation method

High quality transparent conducting CuI thin films were deposited at room temperature via thermal evaporation technique followed by post deposition annealing at different temperatures. The samples were characterised by X-ray diffraction (XRD), UV–Vis spectrophotometry, Scanning electron microscopy and I-V measurements. The structural, morphological and optical properties were studied as a function of the annealing temperature from room temperature (RT) to 200 °C. XRD results revealed that the films were polycrystalline with zinc blende structure of cubic phase. Increasing the annealing temperature increased the crystallite size from 33 to 49 nm whilst the dislocation density and lattice strain shifted to lower values. High transmittance of about 70–80% was exhibited by all films in the entire visible spectral range. The as deposited film possesed the lowest resistivity of 3.0×10⁻³ Ω cm.     

Compositional tailoring effect on crystal structure,mechanical and thermal properties of γ-AlON transparent ceramics

In view of the practical application of γ-AlON as a promising transparent structural ceramic, in-depth insight into its mechanical and thermal properties is essential. The solid-state MAS NMR technique was combined with XRD Rietveld refinement to confirm the crystal structure of Al_(8+x)/3O_4-xN_x (x = 0.299–0.575). These structural parameters were further applied to predict hardness and elastic properties based on theoretical exploration, which are in good agreement with the experimental values. A slight enhancement of mechanical properties with increasing nitrogen concentration is attributed to the stronger chemical bond in octahedra. The experimental thermal conductivity of γ-AlON transparent ceramics was improved slightly with the rise of x in the temperature range from 298 K to 1074 K. The intrinsic lattice thermal conductivity was determined by eliminating the extrinsic phonon scattering as well as the thermal radiation. The reason for the discrepancy between experimental and intrinsic thermal conductivity was revealed. The present methods provided powerful and accessible guidelines in optimizing the mechanical and thermal properties of oxynitride materials.     

Effect of lattice structure evolution on the thermal and mechanical properties of Cu–Al2O3/GNPs nanocomposites

In this study, high-energy ball milling accompanied by compaction and sintering were employed for manufacturing Cu-based hybrid nanocomposite reinforced by Al₂O₃ and GNPs. This hybrid nanocomposite is proposed to meet the specification of heat sink applications, where excellent mechanical and thermal performance is demanding. Different processing parameters were experimentally considered such as sintering temperature and weight percentage of GNPs, 0, 0.25, 0.50, 0.75, and 1 wt %. The weight percentage of Al₂O₃ was fixed at 10%. The results demonstrated that the mechanical and thermal performance of the fabricated nanocomposites were superior for nanocomposite containing 0.5% GNPs and sintered at 1000 °C. The hardness, the thermal conductivity and the coefficient of thermal expansion (CTE) were improved by 21%, 16.7%, and 55.2%, respectively, compared to composite without GNPs addition. The improved mechanical and thermal properties were attributed to the low stacking fault energy, small crystallite size, high dislocation density, and low lattice strain of the composite prepared at this composition. Moreover, the better dispersion of the nano-particles of GNPs and Al₂O₃ inside the matrix helped for the strength and thermal conductivity improvement while maintaining low CTE.     

Effect of chemical structure of aromatic dianhydrides on the thermal, mechanical and electrical properties of their terpolyimides with 4,4′-oxydianiline

Aromatic terpolyimides were synthesized by the reaction of 3,3′,4,4′-oxydiphthalicdianhydride(ODPA), 3,3′,4,4′-biphenyldianhydride(BPDA) and 3,3′,4,4′-benzophenonetetracaboxylicdianhydride(BTDA) with 4,4′-oxydianiline(ODA) via thermal imidization with the view to enhance their tensile properties without compromising thermal properties compared to their homo and copolyimides. Their films were characterized by FTIR, TGA, DSC and XRD. Their FTIR spectra established formation of polyimide by the characteristic vibrations at 1375cm⁻¹(C-N stretch) and 1113 cm⁻¹(imide ring deformation). TGA results showed imidization of residual polyamide acid close to 250 °C and decomposition of polyimides at about 540 °C. XRD results showed amorphous nature for all terpolyimides. Their tensile strength and tensile modulus were higher than either homo or copolyimides. Incorporation of BPDA, without bridging groups between the aromatic rings into the backbone of ODPA/BTDA-ODA is suggested as the cause for such an enhancement. Such terpolyimide can find application as adhesives in making flexible single/multilayer polyimide metal-clad laminates in flexible printed circuits and tape automated bonding applications. In addition, the terpolyimide, BPDA/BTDA/ODPA-ODA (mole ratio 0.5:0.25:0.25:1), showed low dielectric constant (3.52) as BPDA could offer slight rigidity by which the orientation of polar groupings could be reduced.     

Effect of zirconia content on mechanical and thermal properties of mullite–zirconia composite

Abstract

Mullite–zirconia composites were prepared by adding various zirconia contents in the mullite ranging from 0 to 30 wt-% and sintering at 1400–1600°C for 2 h. The phase composition examined by X-ray diffraction showed that mullite was the major phase combined with developed t-ZrO₂ and m-ZrO₂ phase as a function of zirconia content, especially at 1600°C, wherein m-ZrO₂ predominated. Density increased when the zirconia content and sintering temperature were increased ranging from 2·2 to 3·53 g cm^?3. The morphology of mullite grain showed elongated grains, whereas dispersed zirconia showed equiaxed and intergranular grains. Flexural strength was continuously improved by adding zirconia during the sintering temperature ranging from 1400 to 1500°C, whereas flexural strength was initially improved up to 5 wt-% of zirconia addition and deteriorated with more than 5 wt-% of zirconia content during sintering between 1550 and 1600°C. The maximum strength, 190 MPa, was obtained when sintering mullite with 30 wt-% of zirconia content at 1500°C. The degradation of strength at high sintering temperature may be a result from more occurrence of m-ZrO₂ phase. Thermal expansion of sintered specimens indicated linear change and hysteresis loop change. The hysteresis loop obtained with increased zirconia content resulted in the t–m phase transformation. Martensitic start temperature M_s was determined to be 530°C for 15 wt-% zirconia sintered at 1500°C, implying that the t–m phase transformation occurred.     

Effect of γ-ray irradiation grafting on the surface property and the bulk structure of M40J fiber

In this study, we aim to improve the surface property and bulk tensile property of M40J graphite fiber by γ-ray co-irradiation treatment of the fiber in epichlorohydrin/acetone mixed solution. The effect of the irradiation treatment was analyzed by X-ray photoelectron spectroscopy, atomic force microscopy, dynamic contact angle test, tensile test, short-beam shear test, scanning electron microscopy, and X-ray diffraction, respectively. The results indicated that the reactive activity, roughness, and interfacial adhesion property of the fiber were improved, and without destroying the bulk structure after the surface irradiation grafting treatment. Mechanical testing results indicated that the tensile strength was decreased slightly; however the tensile module was improved. The γ-ray co-irradiation grafting was an effective method for modifying the physicochemical properties of M40J graphite fiber and improving the interfacial adhesion of its composites.     

Effect of α- and γ-tocopherols on thermal polymerization of purified high-oleic sunflower triacylglycerols

The antipolymerization effects of α- and γ-tocopherols were compared in model systems composed of purified high-oleic sunflower triacylglycerols at 180°C. γ-Tocopherol was much more effective as an antipolymerization inhibitor than α-tocopherol, partly due to lower oxidizability/disappearance. Purified triacylglycerols of sunflower, rapeseed, and high-oleic sunflower oils were less stable than their nonpurified forms containing tocopherols. Results confirmed that tocopherols per se can act as antipolymerization agents in high-oleic oils at frying temperatures. No synergism was observed when α- and γ-tocopherols were present together although larger amounts of residuals were left for both tocols. Results suggested that high-oleic/high-γ-tocopherol oils (such as high-oleic canola and high-oleic soybean oils) may provide better frying oils than high-oleic/high-α-tocopherol oils (such as high-oleic sunflower oil).     

Effect of acid treatment on the composition and structure of a natural aluminosilicate and on its catalytic properties in α-pinene isomerization

The article deals with the effect of the conditions of modification of a natural aluminosilicate catalyst with a 10% HCl solution on the chemical and phase compositions, porous and crystal structures, and acidity of the material and on its catalytic properties in α-pinene isomerization. Treatment of the aluminosilicate with 10% HCl (25–250 mL per gram of solid) causes cation exchange, increases the concentration of protonic sites on the aluminosilicate surface, and removes impurity calcite and dolomite. The specific surface area of the aluminosilicate increases from 52 to 68–82 m²/g. Treatment of the aluminosilicate with 175.0 or 250.0 mL/g of HCl removes a considerable amount framework Al³⁺, Fe^2+/3+, and Mg²⁺ cations, leading to a partial disruption of its structure and to a decrease in its acidity, specific surface area, and, as a consequence, catalytic activity relative to the same parameters of the samples treated with 50 or 100 mL/g of HCl. The highest catalytic activity is displayed by the aluminosilicate treated with 50 mL/g of HCl. The camphene and dipentene selectivity of the reaction (at 85% α-pinene conversion) with the original catalyst is 55 and 30%, respectively; modifying the aluminosilicate with HCl raises the camphene selectivity and reduces the dipentene selectivity by 5–6%. The catalyst considered here is more active than the commercial titanium catalyst.     

Effect of segment structure on the thermal stability of CPVC in the Gas–Solid PVC chlorination process

The chlorination of the polyvinyl chloride resin with different ratios of  CH₂ , CHCl₂, and CCl₂ was carried out through a gas–solid process by varying the temperature, reaction time, and chlorine concentration. The rheological properties and thermal stability of the resin were characterized. ¹³C NMR was used to characterize the segment structure of the resin. In addition, conjugated diene structure was determined by UV–Visible to study its chlorination process. The results show that  CCl₂ units in the structure promote the dehydrochlorination of CPVC, forming a conjugated diene structure and reducing the rheological properties and thermal stability. In contrast, the formation of  CHCl in the chlorination process increased the thermal stability of the resin. Moreover, a structure-effect relationship between the structure and performance has been established, and a stepwise process of chlorination was obtained by analyzing the changes of the structure segment content at different stages.     

Effect of the maleic anhydride content on the structural,thermal, rheological and film properties of the n-butyl methacrylate–maleic anhydride copolymers

Various copolymers of n-butyl methacrylate (nBMA)-maleic anhydride (MA) were synthesized by free radical solution polymerization using xylene as a solvent, with monomer ratio of (nBMA/MA) 80/20, 65/35 and 50/50 wt%. The nBMA/MA copolymers were analyzed by Fourier transform infrared spectroscopy (FTIR), proton nuclear magnetic resonance (¹H NMR), gel permeation chromatography (GPC) differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), rheology, acid value, microhardness and friction resistance. The formation of the nBMA/MA copolymers was proven by FTIR and ¹H NMR. The conversion percentage, glass transition temperature (T_g), thermal stability, hardness and the friction resistance of the nBMA/MA copolymers increased with the MA contents in the copolymers. All copolymers presented a thinning-shear rheological behavior due to the presence of entanglements. All films of the copolymers showed a good chemical resistance to HCl and NaCl solutions, but in the presence of NaOH solutions the films exhibited a blister.     

FT-Raman analysis of the effects of γ-radiation on nylon 6–12 filaments

Summary FT-Raman spectroscopy of commercial amorphous and crystalline nylon 6–12 filaments subjected to various -radiation doses are presented. The results show that a difference exists in the interaction of -radiation with these polyamides, depending on the crystallinity which can be evaluated by measuring the CH-stretching/CH-bending Raman band intensity ratio as a function of applied -dose.     

Effect of annealing on the structure and magnetic properties of mechanically milled TiO2–Fe2O3 mixture

A mixture of Fe₂O₃ and TiO₂ oxides has been mechanically milled to form TiFe₂O₄ spinel phase. X-ray diffraction (XRD) pattern of the as-milled mixture shows the presence of both Fe₂O₃ and TiO₂ phases. The diffraction peaks become broader and their relative intensity drastically decreases due to the particle size reduction and accumulation of strains. The milled powder was then subjected to annealing at different temperatures (600, 750, 900, 1200 °C). Annealing at 600 °C and 750 °C does not show any significant change in the phase formation. Nonetheless, XRD patterns show a narrowing and an increase in the intensity of Fe₂O₃ peaks with respect to TiO₂, which was reflected by an evolution in particle nano-structure following SEM analysis. An increase in the intensity ratio of the major peaks belonging to Fe₂O₃ relative to the as-milled mixture, which was associated with a reduction of the amount of TiO₂, suggested a possible insertion of Ti into the Fe₂O₃ crystal lattice. However, in VSM measurements, annealing at 600 °C and 750 °C does not change the ferromagnetic phase but the effect of annealing was a notable reduction in the values of both Ms and Mr (saturation magnetization and remanence magnetization respectively) Ultimately, as the powder was heated to 900 °C a new phase seemed to have emerged, this phase was confirmed by SEM, XRD, and magnetic measurements (VSM) where it change phase from ferromagnetic to paramagnetic phase.     

Effects of the Ar flow rate on the composition,structure, and properties of near-stoichiometric SiC fibres that were annealed at 1600°C

SiC fibres are widely used in the aerospace and nuclear fields due to their unique high-temperature resistance. Maintaining excellent high-temperature resistance is necessary for the application of fibres. This study involved processing nearly stoichiometric SiC fibres in Ar at 1600 °C for 1 h. The effects of the Ar flow rate on the composition, structure, and properties of fibres after high-temperature treatment were investigated by elemental analysis, SEM, EDS, TEM, XRD, and Raman spectroscopy. The results showed that the nearly stoichiometric SiC fibres did not undergo noticeable pyrolysis or active oxidation at a low Ar flow rate (<0.2 L/min) with a weight loss rate of less than 1% and that the tensile strength retention rate was as high as 86%. As the Ar flow rate was gradually increased above 0.2 L/min, an active oxidation reaction occurred, and the reaction products of SiO and CO were deposited on the fibre surfaces to form large SiC grains. The fibres gradually evolved into a skin-care structure, and the mechanical properties degraded rapidly. A high-temperature inert gas environment with a low flow rate is very important for preserving the mechanical properties of near-stoichiometric SiC fibres at high temperatures.     

Effect of lattice structure evolution and stacking fault energy on the properties of Cu–ZrO2/GNP nanocomposites

A hybrid nanocomposite comprising nanosized ZrO₂ and graphene nanoplatelet (GNP)-reinforced Cu matrix was synthesised via powder metallurgy. The influence of sintering temperature and GNP content on the electrical and mechanical behaviour of the Cu–ZrO₂/GNP nanocomposite was investigated. The ZrO₂ concentration was fixed at 10% for all the composites. Upon increasing the GNP concentration up to 0.5%, a significant improvement was observed in the compressive strength, microhardness, and electrical conductivity of the composite. Furthermore, the properties were significantly improved by increasing the sintering temperature from 900 to 1000 °C. The compressive strength, hardness, and electrical conductivity of Cu–10%ZrO₂/0.5%GNP were higher than those of the Cu–ZrO₂ nanocomposite by 60, 21, and 23.8%, respectively. This improvement in the mechanical properties is because of the decrease in the crystallite size and dislocation spacing, which increases the dislocation density, thereby increasing the impedance towards dislocation movement. The lower stacking fault energy of the hybrid nanocomposites enables easier electron transfer within and between the Cu grains, resulting in an improved electrical conductivity. The enhancement in strength and electrical conductivity were aided by the GNPs and ZrO₂ nanoparticles that were dispersed widely in the Cu matrix.