Temperature and variable strain rate sensitivity in recycled HDPE

The recycling of post-consumer plastics and their utilization as raw materials to develop value-added products has become an important goal worldwide. The present work is concerned with the thermo-mechanical analysis of recycled high-density polyethylene (HDPE) under uniaxial tensile loading. The main focus is to propose a one-dimensional phenomenological model able to describe the influence of temperature and strain rate on the mechanical behavior. Tensile tests were performed over a wide range of temperatures (from 25°C to 100°C). Each experiment was performed under controlled strain rate varying from 7.25 × 10⁻⁵ s⁻¹ to 7.25 × 10⁻³ s⁻¹ in steps. It is shown that only one tensile test performed at three different temperatures is necessary to fully identify experimentally all material parameters that arise in the theory. Thus, with this experimental procedure, the number of tests used to evaluate the mechanical properties of recycled HDPE is significantly reduced. The experiments are compared with the model predictions and show good agreement.     

Tensile properties of semi-crystalline thermoplastic polymers: Effects of temperature and strain rates

This work deals with the study of temperature and time dependency of tensile properties of a PA 12-based polymer. The range of variation of parameters in experiments was linked to in-service conditions of components manufactured with this material (temperature interval from ?25 °C to 50 °C and average strain-rate magnitudes from 0.00028 s^?1 to 9.4 s^?1). For tests with different temperatures and low speed, an electro-mechanical machine, Zwick Z250, equipped with an incremental extensometer was used. To study the effect of strain rate at medium speeds, a servo-hydraulic system, Schenk PC63M, equipped with a strain-gauge extensometer was used, while at high speeds a servo-hydraulic machine, Instron VHS 160/20, equipped with a high-speed camera for strain evaluation by digital image correlation was employed. The changes of the rate of deformation with strain as well as elastic modulus variation with strain were studied. An increase in the elastic modulus and yield strength was observed with a drop in temperature and an increase in the strain-rate, temperature having a stronger influence on the variation of mechanical properties. The collected data was assembled in an elasto-plastic material model for finite-element simulations capable of rendering temperature- and strain-rate-dependency. The model was implemented in the commercial software Abaqus, yielding accurate results for all tests.     

Tensile mechanical properties of basalt fiber reinforced polymer composite under varying strain rates and temperatures

High-strength woven fabrics and polymers are ideal materials for use in structural and aerospace systems. It is very important to characterize their mechanical properties under extreme conditions such as varying temperatures, impact and ballistic loadings. In this present work, the effects of strain rate and temperature on the tensile properties of basalt fiber reinforced polymer (BFRP) were investigated. These composites were fabricated using vacuum assisted resin infusion (VARI). Dynamic tensile tests of BFRP coupons were conducted at strain rates ranging from 19 to 133 s⁻¹ using a servo-hydraulic high-rate testing system. Additionally, effect of temperature ranging from −25 to 100 °C was studied at the strain rate of 19 s⁻¹. The failure behaviors of BFRP were recorded by a Phantom v7.3 high speed camera and analyzed using digital image correlation (DIC). The results showed that tensile strength, toughness and maximum strain increased 45.5%, 17.3% and 12.9%, respectively, as strain rate increased from 19 to 133 s⁻¹. Moreover, tensile strength was independent of varying temperature up to 50 °C but decreased at 100 °C, which may be caused by the softening of epoxy matrix and weakening of interfaces between fibers and matrix when the glass transition temperature was exceeded.     

Elasto-viscoplastic behaviour of a polyvinylidene fluoride (PVDF) in tension

The present paper is concerned with the plasticity of a polyvinylidene fluoride (PVDF) in tension. Strain rate strongly influences the plastic behaviour, but the variation of the elastic properties is almost negligible within the range of strain rates considered in the study (from 1.6 × 10⁻⁴ s⁻¹ up to 1.6 × 10⁻¹ s⁻¹). In particular, the yield stress and the ultimate tensile strength are strongly rate-dependent. A one-dimensional elasto-viscoplastic phenomenological model is proposed and analysed. Despite the nonlinearity of the model equations, only one tensile test performed with variable strain rate is sufficient to identify all material parameters. Model predictions are compared with experiments showing good agreement.     

Experimental investigation and constitutive modeling of the deformation behavior of Poly-Ether-Ether-Ketone at elevated temperatures

The present study investigates the deformation behavior of Poly-Ether-Ether-Ketone (PEEK) at elevated temperatures and low strain rates through a combination of experiments and simulations. Uniaxial tension tests at elevated temperatures (293–543 K) and strain rates (8.3 × 10⁻³ to 3.3 × 10⁻¹ s⁻¹) were performed, and the temperature- and rate-dependencies of the deformation behavior and mechanism of PEEK were discussed in detail. The Erichsen test was performed at temperatures varying from 473 to 533 K and a fixed speed of 1 mm/s. Based on an investigation of numerous constitutive models, a phenomenological model called DSGZ was employed in ABAQUS/Explicit to characterize the deformation behavior of PEEK at elevated temperatures, and the deviation between experimental and simulation data was less than 10% at large deformations. Moreover, the simulation results accurately predicted the necking and cold drawing phenomena in the tension test as well as the deformation in the Erichsen test.     

Effects of humidity on Young's modulus in poly(methyl methacrylate)

Tensile tests on poly (methyl methacrylate) (PMMA) were conducted to clarify the effects of humidity and strain rate on tensile properties, particularly Young's modulus. Prior to the tensile tests, specimens were kept under various humidity conditions at 293 K, which were the same as the test conditions, for a few months to adjust the sorbed water content in the specimens. The tensile tests were performed under each humidity condition at three different strain rates (approximately 1.4 × 10^?3, 1.4 × 10^?4, and 1.4 × 10^?5 s^?1). Stress‐strain curves changed with humidity and strain rate. Young's moduli were also measured at small applied stresses (below 6.7 MPa) under various humidity conditions at 293 K. Young's modulus decreases linearly with increasing humidity and a decreasing logarithm of strain rate. These results suggest that Young's modulus of PMMA can be expressed as a function of two independent parameters that are humidity and strain rate. A constitutive equation for Young's modulus of PMMA was proposed. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 460–465, 2002; DOI 10.1002/polb.10107     

Different Photosynthetic Responses of Pyropia yezoensis to Ultraviolet Radiation Under Changing Temperature and Photosynthetic Active Radiation Regimes

Macroalgae play a crucial role in coastal marine ecosystems, but they are also subject to multiple challenges due to tidal and seasonal alterations. In this work, we investigated the photosynthetic response of Pyropia yezoensis to ultraviolet radiation (PAR: 400–700 nm; PAB: 280–700 nm) under changing temperatures (5, 10 and 15°C) and light intensities (200, 500 and 800 μmol photons m^?2 s^?1). Under low light intensity (200 μmol photons m^?2 s^?1), P. yezoensis showed the lowest sensitivity to ultraviolet radiation, regardless of temperature. However, higher temperatures inhibited the repair rates (r) and damage rates (k) of photosystem II (PSII) in P. yezoensis. However, under higher light intensities (500 and 800 μmol photons m^?2 s^?1), P. yezoensis showed higher sensitivity to UV radiation. Both r and the ratio of repair rate to damage rate (r:k) were significantly inhibited in P. yezoensis by PAB, regardless of temperature. In addition, higher temperatures significantly decreased the relative UV‐inhibition rates, while an increased carbon fixation rate was found. Our study suggested that higher light intensities enhanced the sensitivity to UV radiation, while higher temperatures could relieve the stress caused by high light intensity and UV radiation.     

Hot tensile fracture characteristics and constitutive modelling of polyether-ether-ketone (PEEK)

The effects of strain rate and deformation temperature on the deformation behaviors of polyether-ether-ketone (PEEK) were studied by uniaxial tensile tests with the temperature range of 23–150 °C and strain rate of 0.01–1 s⁻¹. The effects of deformation temperature and strain rate on the hot tensile deformation behavior and fracture characteristics were investigated by scanning electron microscope (SEM) and discussed in detail. SEM experimental results suggest that fracture morphology is not strain rate sensitive but temperature sensitive. Based on the tensile results, the Johnson-Cook and modified Johnson-Cook constitutive models were established for PEEK. Furthermore, a comparative study has been made on the accuracy and effectiveness of the developed models to predict the flow stress. The results show that the original Johnson-Cook model reflects the deformation behavior more accurately throughout the entire test temperature and strain rate range under uniaxial tensile conditions.     

Rapid solidification of cobalt melt by molecular dynamics simulation

Molecular dynamics simulation was applied to investigating the evolvement rule of cobalt melt microstructure during solidification at different cooling rates. The cooling rate for the formation of amorphous phase is determined by analyzing the radial distribution function, the H–A bond-type index and the mean square displacement. The simulation results showed that the nucleation undercooling increases with the initial temperature, and in the undercooling versus temperature curve, there are two inflection points. Besides, when the initial temperature reaches 2450 K, the undercooling will be stabilized at 1061 K. As the cooling rate is less than 1.0?×?10^11.0 K s^?1, the FCC and HCP crystal structures will be obtained. Amorphous structure will be obtained if the cooling rate is more than 1.0?×?10^13.0 K s^?1. If the cooling rate of the Co melt is between 1.0?×?10^11.0 and 1.0?×?10^13.0 K s^?1, the crystal and amorphous structures will be coexistent, which indicates that the critical cooling rate of crystal–amorphous transition is 1.0?×?10^11.0 K s^?1.

     

Influence of strain rate on the compressive yield stress of CMDB propellant at low,intermediate and high strain rates

The mechanical properties of composite modified double base (CMDB) propellant significantly depend on the strain rate. In particular, the yield stress increases dramatically at higher strain rates. To study this behaviour, low, intermediate and high strain rate compression testing (1.7 × 10⁻⁴ to 4 × 10³ s⁻¹) of CMDB propellant at room temperature was conducted by using a universal testing machine, a hydraulic testing machine and a split Hopkinson pressure bar (SHPB) system, respectively. The yield stress was observed to increase bilinearly with the logarithm of strain rate, with a sharp increase in slope at a strain rate of 5 × 10¹ s⁻¹, which was supported by dynamic mechanical analysis (DMA) testing. The Ree-Eyring model, involving two rate-activated processes, was employed to predict the yield behaviour of CMDB propellant over a wide range of strain rates. The predictions are in excellent agreement with the experimental data.     

Cationic polymerization of styrenes by activated covalent species. Direct 1H-NMR observation of complexes of 1-phenylethyl acetates with lewis acids

Complexes of boron trichloride, boron tribromide, and ethylaluminumdichloride with various acetates were directly observed by ¹H-NMR. Complexes of secondary and tertiary acetates which model macromolecular active species in polymerization of styrene and isobutene are stable at ?75°C, but decompose at temperatures above ?30°C to yield corresponding chlorides or bromides. The stability of complexes depends on the Lewis acid, the alkyl group in the ester, and the structure of acetate. Rates of the bimolecular exchange of complexes with excess acetate were calculated from dynamic NMR to be k_ex = 2 × 10¹ L mol^?1 s^?1 (?65°C) and k_ex = 5 × 10⁴ L mol^?1 s^?1 (?75°C) for 1-phenylethyl acetate with BCl₃ and EtAlCl₂, respectively.     

Kinetics and mechanism of oxidation of glycine,alanine, and threonine by fluoride coordinated bismuth(V) in aqueous HClO4–HF medium

The kinetics of oxidation of amino acids viz. glycine, alanine, and threonine with bismuth(V) in HClO₄–HF medium have been studied. The kinetics of the oxidation of all these amino acids exhibit similar rate laws. The second-order rate constants were calculated to be 2.04 × 10^?2 dm³ mol^?1 and 2.72 × 10^?2 dm³ mol^?1 s^?1 for glycine and alanine, respectively, at 35°C and 5.9 × 10^?2 dm³ mol^?1 s^?1 for threonine at 25°C. All the possible reactive species of both bismuth(V) and amino acids have been discussed and a most probable kinetic model in each reaction has been envisaged. © 1994 John Wiley & Sons, Inc.     

Ozone reduction at Nafion modified Au electrode and the measurement of ozone concentration in highly resistive solutions

The mass transport and charge transfer kinetics of ozone reduction at Nafion coated Au electrodes were studied in 0.5 mol/L H2SO4 and highly resistive solutions such as distilled water and tap water. The diffusion coefficient and partition coefficient of ozone in Nafion coating are 1.78×10-6 cm2·s-1 and 2.75 at 25℃ (based on dry state thickness), respectively. The heterogeneous rate constants and Tafel slopes for ozone reduction at bare Au are 4.1×10-6 cm·s-1, 1.0×10-6 cm·s-1 and 181 mV, 207 mV in 0.5 mol/L H2SO4 and distilled water respectively and the corresponding values for Nafion coated Au are 5.5×10-6 cm·s-1, 1.1×10-6 cm·s-1 and 182 mV, 168 mV respectively. The Au microelectrode with 3 μm Nafion coating shows good linearity over the range 0-10 mmol/L ozone in distilled water with sensitivity 61 μA·ppm-1 ·cm-2, detection limit 10 ppb and 95% response time below 5 s at 25℃. The temperature coefficient in range of 11-30℃ is 1.3%.     

Electrochemical reduction of ytterbium in perchloric media

The electrochemical behavior of Yb³⁺ in perchloric media was studied by cyclic voltammetry and current reversal chronopotentiometry at several temperatures. The results show that the reversible electrochemical reduction of Yb³⁺ is followed by homogeneous reactions. The experimentally determined diffusion coefficients of ytterbic ion are 0.41×10^?5, 0.48×10^?5 and 0.53×10^?5 cm² s^?1 at 4.2, 9.2 and 14.7°C, respectively, in 0.5 M NaClO₄ solutions. From these data a value of 16 kJ mol^?1 (3830 cal mol^?1) was obtained for the activation energy for diffusion of ytterbic ion. From the activation energy the diffusion coefficient of ytterbic ion at 25.0°C was estimated. The value of 0.67×10^?5 cm² s^?1 was obtained. In all the experiments the initial pH was maintained at 4.1.     

Reply to comment on the possible role of the reaction H+H2O→H2+OH in the radiolysis of water at high temperatures

In reply to “Comment on the possible role of reaction H+H₂O→H₂+OH in the radiolysis of water at high temperatures” (Bartels, 2009 Comment on the possible role of the reaction H+H₂O→H₂+OH in the radiolysis of water at high temperatures. Radiat. Phys. Chem. 78, 191–194) we present an alternative thermodynamic estimation of the reaction rate constant k. Based on the non-symmetric standard state convention we have calculated that the Gibbs energy of reaction Δ_rG=57.26 kJ mol^?1 and the reaction rate constant k=7.23×10^?5 M^?1 s^?1 at ambient temperature. Re-analysis of the thermodynamic estimation (Bartels, 2009 Comment on the possible role of the reaction H+H₂O→H₂+OH in the radiolysis of water at high temperatures. Radiat. Phys. Chem. 78, 191–194) showed that the upper limit for the rate constant at 573 K is k=1.75×10⁴ M^?1 s^?1 compared to the value predicted by the diffusion-kinetic modelling (3.18±1.25)×10⁴ M^?1 s^?1 (Swiatla-Wojcik, D., Buxton, G.V., 2005. On the possible role of the reaction H+H₂O→H₂+OH in the radiolysis of water at high temperatures. Radiat. Phys. Chem. 74(3–4), 210–219). The presented thermodynamic evaluation of k(573) is based on the assumption that k can be calculated from Δ_rG and the rate constant of the reverse reaction which, as discussed, are both uncertain at high temperatures.     

Studies on some radical transfer reactions by entrapping the radicals as polymer endgroups. III. Reaction of ȮH radical with halide ions

The reactions of OH radical with Cl^?, Br^?, I^?, and F^? ions have been studied by entrapping the product radicals as polymer endgroup which have been detected and estimated by the sensitive dye partition technique. The rate constants of the reactions with Br^?, Cl^?, and F^? ions have been determined to be 1.51 × 10⁹, 1.32 × 10⁹, and 0.92 × 10⁹ L mol^?1 s^?1, respectively at 25°C and pH 1.00. Oxidation of I^? ions liberates I, which inhibits the polymerization and the reaction could not be followed by polymer endgroup analysis. The observed order of reactivity Br^? > Cl^? > F^? is in accordance with the electron affinities of the halide ions. The acidity of the reaction medium has a strong influence on the rate of reaction. With Br^? ions, the rate constant of the reaction falls from 1.51 × 10⁹ to 0.75 × 10⁹ L mol^?1 s^?1 at 25°C as the pH is raised from 1.0 to 2.8. The method is simple and accurate and can be applied to study very reactive radicals.     

Tensile properties of ultradrawn polyethylene

High-density polyethylene filaments prepared by a solid-state deformation in an Instron capillary rheometer show unusually high crystal orientation, chain extension, axial modulus, and ultimate tensile strength. The Young's modulus and ultimate tensile strength have been determined from stress–strain curves. Gripping of this high modulus polyethylene has been a problem heretofore, but the measurement of ultimate tensile strength has now been made feasible by a special gripping procedure. Tensile moduli show an increase with sample preparation temperature and pressure. Values as high as 6.7 × 10¹¹ dyne/cm² are obtained from samples extruded at 134°C and 2400 atm and tested at a strain rate of 3.3 × 10^?4 sec^?1. The effect of strain rate and frequency on modulus has also been evaluated by a combination of stress–strain data and dynamic tension plus sonic measurements over nine decades of time.     

Organocobalt chelates as initiators of emulsion polymerization of styrene

The kinetics of decomposition of organocobalt chelates in the pH range of 2.2–7.0 has been studied. It has been shown that the rate constant of decomposition of the octyl chelate complex at 20°C changes from ～3 × 10^?3 to ～6 × 10^?6 s^?1 in the above pH range. The rate constants of decomposition of complexes with ethyl, octyl, and cetyl ligands, as estimated at 20°C and pH 8.3, are 1.69 × 10^?4, 1.39 × 10^?4, and 2.42 × 10^?5 s^?1, respectively. As evidenced by emission spectrometry measurements, ～100% of organocobalt chelates with ethyl and isopropyl ligands occur in the aqueous phase, while organocobalt chelates with octyl and cetyl ligands are partitioned between monomer and aqueous phases. The rates of initiation of the emulsion polymerization of styrene have been measured by the inhibited polymerization procedure. It has been demonstrated that among three tested compounds (diphenyl picryl hydrazyl, hydroquinone, and benzoquinone), benzoquinone has been found to be a suitable inhibitor for the polymerization under study. The rates of initiation of styrene polymerization at 30°C for organocobalts with ethyl, octyl, and cyclohexyl ligands are 1.0 × 10^?7, 1.04 × 10^?7, and 3.7 × 10^?6 mol/(l s), respectively. The rate constant of decomposition of the organocobalt complex with the octyl ligand at 30°C is 2.28 × 10^?5 s^?1, and the efficiency of initiation with this complex is 0.95.     

Proton NMR studies of lanthanum nickel hydride: Structure and diffusion

The proton magnetic resonance spectrum of lanthanum nickel hydride LaNi_5.3H₆ was measured over the temperature range 118°K < T < 300°K. The second moment of the absorption at 118°K is M₂ = 13.4 ± 0.3 G². Several possible arrangements of the hydrogen atoms are discussed. Narrowing of the line above 140°K is analyzed in terms of proton diffusion and gives an activation enthalpy E = 21 ± 1 kJ mol^?1, NMR correlation time pre-exponential 0.2 ps < τ_c⁰ < 1.6 ps and a self diffusion coefficient at 300°K of 2 × 10^?12 m² s^?1 < D < 2 × 10^?11 m² s^?1.