Structure–property relationships in ternary polymer blends with core–shell inclusions: revisiting the critical role of the viscosity ratio

Structure–property relationship in typical polypropylene/polycarbonate/poly[styrene-b-(ethylene-co-butylene)-b-styrene] (PP/PC/SEBS) ternary blends containing maleated SEBS (SEBS-g-MAH) was investigated. Three grades of PC with different melt viscosities were used, and changes in blend morphology from PC/SEBS core–shell particles partially surrounded by SEBS-g-MAH to inverse SEBS/PC core–shell particles in PP matrix were observed upon varying the viscosity ratio of PC to SEBS. It was found that the viscosity ratio completely controls the size of the core–shell droplets and governs the type, population, and shape of the dispersed domains, as evidenced by rheological, mechanical, and thermomechanical behavioral assessments. Dynamic mechanical analysis of samples with common (PC–SEBS) and inverse (SEBS–PC) core–shell particles revealed that they show completely different behaviors: blends containing PC–SEBS presented a higher storage and loss modulus, while blends containing SEBS–PC exhibited a lower β-transition temperature. Moreover, ternary blends with PC cores showed the highest Young’s modulus values and the lowest impact strength, due to the different fracture modes of the blends containing PC–SEBS and SEPS–PC core–shell droplets, which present debonding and shell-fracture mechanisms, respectively. Morphological observations of blends with high-molecular-weight PC demonstrated the presence of detached droplets and rods of PC in the PP matrix, along with composite core–shell and rod-like particles. Micrographs of the fracture surfaces confirmed the proposed mechanisms, given the presence of stretched (debonded) PC (SEBS) cores encapsulated by SEBS (PC), which require more (less) energy to achieve fracture. The correlation between the mechanical and morphological properties proves that decreasing core diameter and shell thickness has positive effects on the impact strength but decreases the Young’s modulus.     

Evolution of quantum correlations in the open quantum systems consisting of two coupled oscillators

The open quantum systems consisting of coupled and uncoupled asymmetric oscillators are considered with an initial quantum-dot trapped-ion coherent state. The quantum correlations between spatial modes of this trapped ion are examined to find their dependence on the temperature, asymmetric parameter, dissipation coefficient and the magnetic field. It is observed that the discord of the initial state is an increasing function of the asymmetric parameter and the magnetic field. Moreover, in the case of two uncoupled modes, entanglement and discord are decreasing functions of temperature and the dissipation coefficient. However, as the temperature and dissipation coefficient increase, the discord fades out faster. In the case of two coupled modes, as the temperature and dissipation coefficient increase, the sudden death of the entanglement and fade out of the discord happen sooner; moreover, as the magnetic field increases, the entanglement sudden death and the discord fade out time occur sooner. Also, with the increase in the asymmetric parameter, the entanglement sudden death is postponed. In addition, in the asymmetric system, appreciable discord can be created in the temperature range 0–10 K, while appreciable entanglement can be created in the temperature range 0–5 mK. Finally, it is observed that non-monotonic evolution of quantum correlations is due to coupling of modes.     

Peering through the lens of high-reliability theory: A competencies driven security culture model of high-reliability organisations

To improve organisational safety and enhance security efficiency, organisations seek to establish a culture of security that provides a foundation for how employees should approach security. There are several frameworks and models that provide a set of requirements for forming security cultures; however, for many organisations, the requirements of the frameworks are difficult to meet, if not impossible. In this research, we take a different perspective and focus on the core underlying competencies that high-reliability organisations (HROs) have shown to be effective in achieving levels of risk tolerance consistent with the goals of a security culture. In doing so we draw on high-reliability theory to develop a Security Culture Model that explains how a firm's supportive and practical competencies form its organisational security culture. To refine and test the model, we conducted a developmental mixed-method study using interviews and survey data with professional managers involved in the information security (InfoSec) programs within their respective HROs. Our findings emphasise the importance of an organisation's supportive and practical competencies for developing a culture of security. Our results suggest that organisations' security cultures are a product of their InfoSec practices and that organisational mindfulness, top management involvement and organisational structure are key to the development of those practices.     

A DEA approach for comparing solution efficiency in U-line balancing problem using goal programming

Line balancing problem plays an important role in the decision making process to increase efficiency and productivity. Recently, U-shaped layout in many production lines has replaced the traditional straight line layout using just-in-time concept. Here, we propose a model, using multi-objective decision making approach to the U-shaped line balancing problem, to offer enhanced decision maker flexibility, by allowing for conflicting goals. The assembly line operation efficiency is the most significant aim in our study, and this efficiency relates to management of resources and the solution of line balancing problem. First, the U-shaped line balancing problem is solved considering the model's goals. Then, the index function of assembly line balancing is determined and the efficiencies of the optimal solution outputs are evaluated using data envelopment analysis (DEA). Finally, the discrimination weakness and distribution of illogical weight in simple DEA models are resolved using a mixed method.     

Compatibilization mechanisms of nanoclays with different surface modifiers in UCST blends: Opposing effects on phase miscibility

The effects of organically modified and pristine nanoclays on the kinetics of thermodynamic equilibrium state attainment for semicrystalline binary blends of polyethylene (PE)/ethylene-vinyl acetate copolymer (EVA) have been investigated. Due to the non-equilibrium compatibilization mechanism, intercalated organoclay results in a slower rate of phase miscibility change at lower annealing temperatures, thereby worsening the PE/EVA compatibility state. In contrast to poorly dispersed pristine nanoclay, the homogeneous state is obtained at higher or equal rates by adding organoclay at higher annealing temperatures because of the dominant role of nanofiller equilibrium compatibilization mechanism. Phase diagrams of these UCST blends determined by a dynamic method shifts to higher temperatures by the incorporation of nanofillers and the unexpected reduction in miscibility window area is much more noticeable for nanocomposites having highly restricted molecular movements. This can verify that dynamic methods lose their efficiency for measuring the equilibrium phase diagram of polymer blends containing nanoparticles.     

Tailoring interfacial adhesion and mechanical performance of biocomposites based on poly(lactic acid)/rice straw by using maleic anhydride through reactive extrusion process

In this study, all-green biocomposites based on poly(lactic acid) (PLA)/rice straw (RS) as an agricultural waste were prepared, and the physical, structural, and mechanical properties of these biocomposites were enhanced by alkali-pulping of RS and chemical grafting of PLA onto the lignocellulosic fiber. The reactive compatibilizers of maleic anhydride grafted PLA (PLA-g-MA) were obtained through a reactive extrusion process at different processing conditions. The probable chemical reactions between the functional groups of PLA-g-MA with hydroxyl groups of RS pulp as well as the end groups of PLA chains can effectively improve the interfacial adhesion between the filler and matrix. However, the findings confirm the great importance of PLA-g-MA chemical structure in controlling the biocomposite performance. By choosing proper processing conditions for preparing PLA-g-MA and incorporating this compatibilizer into the PLA/treated RS biocomposite, Young modulus, tensile strength, impact strength, and tensile toughness of the PLA/RS biocomposite increased by 101%, 156%, 96%, and 327%, respectively.     

Modeling of glycolysis of flexible polyurethane foam wastes by artificial neural network methodology

The glycolysis process as a useful approach to recycling flexible polyurethane foam wastes is modeled in this work. To obtain high quality recycled polyol, the effects of influential processing and material parameters, i.e. process time, process temperature, catalyst‐to‐solvent (Cat/Sol) and solvent‐to‐foam (Sol/Foam) ratios, on the efficiency of the glycolysis reaction were investigated individually and simultaneously. For the continuous prediction of process behavior and interactive effects of parameters, an artificial neural network (ANN) model as an efficient statistical‐mathematical method has been developed. The results of modeling for the criteria that determine the glycolysis process efficiency including the hydroxyl value of the recycled polyol and isocyanate functional group conversion prove that the adopted ANN model successfully anticipates the recycling process responses over the whole range of experimental conditions. The Cat/Sol ratio showed the strongest influence on the quality of the recycled polyol among the studied parameters, where the minimum hydroxyl value was obtained at a medium amount of the assigned ratio. For the consumed polyurethane foam, a higher value of this ratio led to an increase in the hydroxyl value and isocyanate conversion. © 2015 Society of Chemical Industry