Combined continuum damage‐embedded discontinuity model for explicit dynamic fracture analyses of quasi‐brittle materials

In this paper, a novel constitutive model combining continuum damage with embedded discontinuity is developed for explicit dynamic analyses of quasi‐brittle failure phenomena. The model is capable of describing the rate‐dependent behavior in dynamics and the three phases in failure of quasi‐brittle materials. The first phase is always linear elastic, followed by the second phase corresponding to fracture‐process zone creation, represented with rate‐dependent continuum damage with isotropic hardening formulated by utilizing consistency approach. The third and final phase, involving nonlinear softening, is formulated by using an embedded displacement discontinuity model with constant displacement jumps both in normal and tangential directions. The proposed model is capable of describing the rate‐dependent ductile to brittle transition typical of cohesive materials (e.g., rocks and ice). The model is implemented in the finite element setting by using the CST elements. The displacement jump vector is solved for implicitly at the local (finite element) level along with a viscoplastic return mapping algorithm, whereas the global equations of motion are solved with explicit time‐stepping scheme. The model performance is illustrated by several numerical simulations, including both material point and structural tests. The final validation example concerns the dynamic Brazilian disc test on rock material under plane stress assumption. Copyright © 2014 John Wiley & Sons, Ltd.     

Natural Palm Olein Polyol as a Replacement for Polyether Polyols in Viscoelastic Polyurethane Foam

The impact of replacing three polyether polyols with different levels of a single palm olein‐based natural oil polyol (NOP) was systematically correlated with the changes in foaming reactivity, cell structure, physico‐mechanical properties, and morphology of viscoelastic (VE) foams. The data show that replacing the polyether polyols with the NOP slightly increased the rate of the foaming reactivity. Increasing the NOP content resulted in increased cell size and cells remained fully open. Increased NOP content contributed to higher load bearing properties of VE foam, which can be attributed to higher functionality of NOP compared to polyether polyols. Addition of the NOP slightly increased the resilience of the foams, however, the hysteresis which is the measure of energy absorption remained mostly unaffected. Age properties, characterized by dry and humid compression sets, were mostly unaffected by the replacement of the polyether polyol with the NOP. The addition of NOP did not impact the morphology of the VE foam polymer matrix, which appears to retain a low degree of hard and soft segment domain separation. Overall, the results demonstrate a feasibility that the NOP can be used to partially replace the polyether polyols in VE polyurethane foams without significant impact on the functional performance.     

Numerical investigation for the suitable choice of bubble diameter correlation for EMMS/bubbling drag model

Mesoscale bubbles exist inherently in bubbling fluidized beds and hence should be considered in the constitutive modeling of the drag force. The energy minimization multiscale bubbling (EMMS/bubbling) drag model takes the effects of mesoscale structures (i.e., bubbles) into the modeling of drag coefficient and thus improves the coarse-grid simulation of bubbling and turbulent fluidized beds. However, its dependence on the bubble diameter correlation has not been thoroughly investigated. The hydrodynamic disparity between homogeneous and heterogeneous fluidization is accounted for by the heterogeneity index,H_d, which can be affected by choice of bubble diameter correlation. How this choice of bubble diameter correlation influences the model prediction calls for further fundamental research. This article incorporated seven different bubble diameter correlations into EMMS/bubbling drag model and studied their effects onH_d. The performance of these correlations has been compared with the correlation used previously by EMMS/bubbling drag model. We found that some of the correlations predicted lower H_d by order of a magnitude than the correlation used by the original EMMS/bubbling drag. Based on such analysis, we proposed a modification in the EMMS drag model for bubbling and turbulent fluidized beds. A computational fluid dynamics (CFD) simulation using two-fluid model with the modified EMMS/bubbling drag model was performed for two bubbling and one turbulent fluidized beds. Voidage distribution, time averaged solid concentration and axial solid concentration profiles were studied and compared with the previous version of the EMMS/bubbling drag model and experimental data. We found that the right choice of bubble diameter correlations can significantly improve the results for CFD simulations.     

Silicon Seed Priming Combined with Foliar Spray of Sulfur Regulates Photosynthetic and Antioxidant Systems to Confer Drought Tolerance in Maize (Zea mays L.)

Silicon - The present study evaluated the effect of silicon (Si) seed priming and sulfur (S) foliar spray on drought tolerance of two contrasting maize hybrids viz. drought tolerant Hi-Corn 11 and...     

Rational design on photoelectrodes and devices to boost photoelectrochemical performance of solar-driven water splitting: a mini review

As an eco-friendly, efficient, and low-cost technique, photoelectrochemical water splitting has attracted growing interest in the production of clean and sustainable hydrogen by the conversion of abundant solar energy. In the photoelectrochemical system, the photoelectrode plays a vital role in absorbing the energy of sunlight to trigger the water splitting process and the overall efficiency depends largely on the integration and design of photoelectrochemical devices. In recent years, the optimization of photoelectrodes and photoelectrochemical devices to achieve highly efficient hydrogen production has been extensively investigated. In this paper, a concise review of recent advances in the modification of nanostructured photoelectrodes and the design of photoelectrochemical devices is presented. Meanwhile, the general principles of structural and morphological factors in altering the photoelectrochemical performance of photoelectrodes are discussed. Furthermore, the performance indicators and first principles to describe the behaviors of charge carriers are analyzed, which will be of profound guiding significance to increasing the overall efficiency of the photoelectrochemical water splitting system. Finally, current challenges and prospects for an in-depth understanding of reaction mechanisms using advanced characterization technologies and potential strategies for developing novel photoelectrodes and advanced photoelectrochemical water splitting devices are demonstrated.     

Vapor-liquid equilibrium of ethanol/ethyl acetate mixture in ultrasonic intensified environment

A vapor-liquid equilibrium (VLE) study was conducted on ethanol/ethylacetate mixture as a preliminary step towards developing an ultrasonic-assisted distillation process for separating azeotropic mixtures. The influence of ultrasonic intensity and frequency on the vapor-liquid equilibrium (VLE) of the mixture was examined using a combination of four ultrasonic intensities in range of 100–400W/cm² and three frequencies ranging from 25–68 kHz. The sonication was found to have significant impacts on the VLE of the system as it alters both the relative volatility and azeotrope point, with preference to lower frequency operation. A maximum relative volatility of 2.32 was obtained at an intensity of 300 W/cm2 and a frequency of 25 kHz coupled with complete elimination of ethanol-ethyl acetate azeotrope. Results from this work were also congruent with some experimental and theoretical works presented in the literature. These findings set a good beginning towards the development of an ultrasonic assisted distillation that is currently in progress.     

Conversion of waste polystyrene through catalytic degradation into valuable products

Waste expanded polystyrene (EPS) represents a source of valuable chemical products like styrene and other aromatics. The catalytic degradation was carried out in a batch reactor with a mixture of polystyrene (PS) and catalyst at 450 °C for 30 min in case of Mg and at 400 °C for 2 h both for MgO and MgCO₃ catalysts. At optimum degradation conditions, EPS was degraded into 82.20±3.80 wt%, 91.60±0.20 wt% and 81.80±0.53 wt% liquid with Mg, MgO and MgCO₃ catalysts, respectively. The liquid products obtained were separated into different fractions by fractional distillation. The liquid fractions obtained with three catalysts were compared, and characterized using GC-MS. Maximum conversion of EPS into styrene monomer (66.6 wt%) was achieved with Mg catalyst, and an increase in selectivity of compounds was also observed. The major fraction at 145 °C showed the properties of styrene monomer. The results showed that among the catalysts used, Mg was found to be the most effective catalyst for selective conversion into styrene monomer as value added product.     

Experimental Comparison of the Effects of Nanometric and Micrometric Particulates on the Tensile Properties and Fracture Behavior of Al Composites at Room and Elevated Temperatures

This article studies the influence of nanometric (n-SiC_p) and micrometric-scale SiC particulates (μ-SiC_p) on the tensile properties of the Al 7075 alloy. The unreinforced Al and its composites were synthesized using the powder metallurgy (P/M) route and were tested uniaxially in tension at both room and elevated temperatures. Aging behavior was studied to observe any effect of the reinforcement on the aging kinetics and hardness of the composites. X-ray diffraction was performed to determine the crystal structures of the raw materials and any reaction phase formed in the composites. The n-SiC_p were not dispersed uniformly in the Al matrix and clustered mainly at the grain boundaries. The stiffness of the composites increased and the ductility decreased with an increase in the volume fraction of the n-SiC_p. The n-SiC_p proved to be a better reinforcement than the traditional μ-SiC_p in terms of imparting higher ductility to the composite. Fractography and microscopy using optical, scanning electron, and transmission electron microscopes were performed for failure and microstructural analysis of all the materials. At room temperature, the fracture altered from ductile in the unreinforced Al to brittle in the composites. At an elevated temperature, the fracture mechanism transformed from brittle to ductile rupture in the composites.     

Copolymerization of carbon monoxide with exo‐methylenecycloalkane and dienes: synthesis of functionalized aliphatic polyketones

Synthesis of functional aliphatic polyketones was achieved by co‐ and terpolymerization of the strained exo‐methylenecycloalkane, methylenecyclopropane (MCP), and also the dienes 1,5‐hexadiene, 1,7‐octadiene and 1,6‐heptadien‐4‐ol, with carbon monoxide and propene, using the dicationic palladium(II) phosphine complex [Pd(dppp) (NCCH₃)₂](BF₄)₂ (I) (dppp is 1,3‐bis(diphenyl‐phosphino)propane) as the catalyst precursor. The resulting MCP/CO copolymer contains both ring‐opened and cyclic microstructures. Ring‐opening copolymerization yields exo‐methylene functionalized polyketone. In contrast to hexadiene/carbon monoxide copolymer (Hx/CO), no ring structures were observed in the alternating octadiene/carbon monoxide (Oc/CO) and heptadien‐4‐ol/carbon monoxide (Hp‐ol/CO) copolymers. The remaining double bonds were left intact to yield polymers with olefinic functionalities in the side chains. © 2001 Society of Chemical Industry