Deformation,yield and fracture of elastomer‐modified polypropylene

In recent decades, great attention has been devoted to the toughening of isotactic poly(propylene) (PP) with elastomers such as ethylene–propylene rubber (EPR). The most important reasons for this interest are the moderate cost and favorable properties of PP. This article is focused on the role of EPR in the deformation and fracture mechanism of PP/EPR blends with different volume fractions of elastomer phase. Differential scanning calorimetry (DSC), tensile tests, and microscopy techniques were used in this study. The fracture mechanism of isotactic PP toughened by EPR (PP/EPR) has also been studied by three point bending (3‐PB) and four point bending (4‐PB) tests. Rubber particle cavitation appears to be the main mechanism of microvoid formation, although some matrix/particle debonding was observed. The investigation of the toughening mechanism shows that a wide damage zone spreads in front of the pre‐crack. Optical microscopy (OM) illustrates that, in pure PP, crazing is the only fracture mechanism, and no evidence of shear yielding is found, while in PP blends craze‐like features associated with shear yielding are observed, which have been identified as high shear localized dilatational bands. This type of deformation pattern supports a model previously proposed by Lazzeri 1 to explain the interparticle distance effect on the basis of the stabilization effect on dilatational band propagation exerted by stretched rubber particles. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 3767–3779, 2003     

Shock-Wave Attenuation and Energy-Dissipation Potential of Granular Materials

The propagation of uniaxial-stress planar shocks in granular materials is analyzed using a conventional shock-physics approach. Within this approach, both compression shocks and decompression waves are treated as (stress, specific volume, particle velocity, mass-based internal energy density, temperature, and mass-based entropy density) propagating discontinuities. In addition, the granular material is considered as being a continuum (i.e., no mesoscale features like grains, voids, and their agglomerates are considered). However, while the granular material is treated as a (smeared-out) continuum, it is recognized that it contains a solid constituent (parent matter), and that the structurodynamic properties (i.e., Equations of State (EOS) and Hugoniot relations) of the granular material are related to its parent matter. Three characteristic shock loading regimes of granular material are considered and, in each case, an analysis is carried out to elucidate shock attenuation and energy dissipation processes. In addition, an attempt is made to identify a metric (a combination of the material parameters) which quantifies the intrinsic ability of a granular material to attenuate a shock and dissipate the energy carried by the shock. Toward that end, the response of a typical granular material to a flat-topped compressive stress pulse is analyzed in each of the three shock loading regimes.     

Influence of PP‐g‐MA on morphology,mechanical properties and deformation mechanism of copolypropylene/clay nanocomposite

Copolypropylene/organoclay nanocomposites are prepared by melt intercalation method in this research. Two different routes for addition of compatibilizer are examined, i.e. addition in the twin‐screw extruder along with the polymer and the clay powder simultaneously and premixing the compatibilizer with the reinforcement in a batch mixer before addition to the polypropylene (PP) matrix. Morphology, tensile and impact properties and deformation mechanisms of the samples made via two procedures are studied and compared with those of the noncompatibilized system. To study the structure of nanocomposites, x‐ray diffraction and transmission electron microscopy techniques are utilized. The deformation mechanisms of different samples are examined via reflected and transmitted optical microscopy. The results reveal that introduction of compatibilizer and also the procedure in which the compatibilizer is added to the compound, affect structure and mechanical properties of nanocomposite. The elastic modulus of PP‐clay nanocomposite has increased 11.5% with incorporation of compatibilizer. Also, introduction of organoclay without compatibilizer facilitates crazing at the notch tip of PP in 3PB testing. Incorporation of compatibilizer, however, makes difficulties in initiation and growth of crazes at the notch tip. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

pH sensitivity and swelling behavior of partially hydrolyzed formaldehyde-crosslinked poly(acrylamide) superabsorbent hydrogels

Poly(acrylamide) superabsorbent hydrogel was synthesized through crosslinking method. Formaldehyde was used as a crosslinking agent. To achieve a hydrogel with high swelling capacity, the resulted hydrogels were saponified using NaOH solution at high temperature. During saponification, ammonia gas is produced from hydrolysis reaction of amide groups. The arising of ammonia produces porous structure in hydrogels, which is confirmed using scanning electron microscopy. The conversion of amide groups to carboxylate groups was identified by FTIR spectroscopy. The reaction variables in both crosslinking and hydrolysis reactions that affect the swelling of hydrogels were optimized. The swelling of the hydrogels in various salt solutions with various valencies and radii was studied. Also, the absorbency under load was measured. The hydrogels exhibited pH-sensitivity characteristics. A sharp swelling change was observed in lieu of pH variations in a wide range (1–13). The swelling variations were explained according to the swelling theory based on the hydrogel chemical structure. The pH-reversibility and on–off switching behavior makes the intelligent hydrogels as good candidates for considering as potential drug carries. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Characterization of minocycline loaded chitosan/polyethylene glycol/glycerol blend films as antibacterial wound dressings

Wound care has been a challenging subject for medical teams and researchers. Bacterial infections are one of the most serious complications in injured skins that often affect healing process. Antibacterial wound dressings can be used to facilitate wound healing process. The purpose of this study is to fabricate chitosan (Chito)/polyethylene glycol (PEG) antibacterial wound dressing doped with minocycline, and to evaluate the influence of composition ratio on the blending properties of the films. To improve the mechanical properties of these films, we examined various amounts of glycerol as a plasticizer. Moreover, we investigated morphological and mechanical aspects, water uptake, degradation, water vapor transmission and wettability properties of the films prepared with various ratios of Chito/PEG/Gly. Assessment of mechanical properties revealed that film containing 80:20 ratio Chito/PEG with 40 PHR Gly content exhibits the highest ultimate tensile strength and elongation at break (9.74 MPa and 45.73% respectively). Furthermore, results demonstrated that upon increasing PEG and Gly contents, degradability and hydrophilicity of the films increased whereas water uptake decreased. Water vapor transmission rate of the films was close to the range of 530–1200 g/m²d, indicating that the as formed films are possible candidates for dressing low exudate wounds or burns. Minocycline loaded films exhibited a biphasic drug release profile and it was more effective on gram-positive bacteria than on gram-negative bacteria. The polymeric film with the highest amount of loaded drug (2%) exhibited insignificant cytotoxicity (88%) against normal fibroblast cell line.     

Corrosion and time dependent passivation of Al 5052 in the presence of H<Subscript>2</Subscript>O<Subscript>2</Subscript>

Corrosion and time–dependent oxide film growth on AA5052 Aluminum alloy in 0.25M Na₂SO₄ solution containing H₂O₂ was studied using electrochemical impedance spectroscopy, potentiodynamic polarization, chronoamperometric and open circuit potential monitoring. It was found that sequential addition of H₂O₂ provokes passivation of AA5052 which ultimately thickens the oxide film and brings slower corrosion rates for AA5052. H2O2 facilitates kinetics of oxide film growth on AA 5052 at 25° and 60 °C which is indicative of formation of a thick barrier film that leads to an increment in the charge transfer resistance. Pitting incubation time increases by introduction of H₂O₂ accompanied by lower pitting and smoother surface morphologies. At short exposure (up to 8 h) to H₂O₂–containing solution, the inductive response at low frequencies predominantly determined the corrosion mechanism of AA5052. On the other hand, at prolonged exposure times (more than 24 h) to 0.25M Na₂SO₄+1vol% H₂O₂ solution, thicker oxide layers resulted in the mixed inductive–Warburg elements in the spectra.     

Toughness Enhancement in Roll-Bonded Al6061-15 vol.% SiC Laminates via Controlled Interfacial Delamination

Researchers have examined different approaches to improve damage tolerance of discontinuously reinforced aluminum (DRA). In this study, three-layer DRA laminates containing two exterior layers of Al6061-15 vol.% SiCp and an interlayer of Al1050 were fabricated by hot roll bonding. Interfacial adhesion between the layers was controlled by means of rolling stain. The results of shear test revealed that, the bonding strength of laminates was influenced by number of rolling passes. Considering this effect, the role of interfacial bonding on the toughness of laminates was studied under three-point bending in the crack divider orientation. The quasi-static toughness of the laminates was greater than that of the monolithic DRA. Plastic deformation of the ductile interlayer and interfacial delamination were found as the major sources of energy absorption in this fracture process. It was shown that interfacial adhesion in these laminate does not alter the initiation energy in quasi-static test. Propagation energy under same loading condition, however, illustrated significant sensitivity to the interfacial bonding. The results of the current study reveal that improving the interfacial adhesion by means of rolling strain eliminates the ease of plastic deformation of the ductile interlayer and thus reduces the contribution of this mechanism in quasi-static toughness of the laminate.     

Nonisothermal suspension polymerization of vinyl chloride for enhanced productivity

In the present study, a mathematical model is developed to numerically predict nonisothermal batch suspension polymerization of vinyl chloride. Free volume theory was used to consider diffusion‐controlled reactions. Model predictions were validated against field data obtained in a pilot scale stirred tank reactor. Variable temperature trajectory was considered during the course of the reaction to improve productivity by reducing the polymerization time for a certain conversion. Variable temperature during the course of the polymerization was successfully implemented by considering the predefined K value. By using variable temperatures during the course of the reaction, the density of the short branches per 1,000 monomer units as a criterion for structure defect remained relatively unchanged. Maximum reduction in reaction time relative to the isothermal case with the same K value and final conversion was 44% for the best temperature trajectory. J. VINYL ADDIT. TECHNOL., 22:470–478, 2016. © 2015 Society of Plastics Engineers     

An efficient parallel algorithm for the longest path problem in meshes

The longest path problem is the problem of finding a simple path with the maximum number of vertices in a given graph, and so far it has been solved polynomially only for a few classes of graphs. This problem generalizes the well-known Hamiltonian path problem, hence it is NP-hard in general graphs. In this paper, first we give a sequential linear-time algorithm for the longest path problem in meshes. Then based on this algorithm, we present a constant-time parallel algorithm for the problem, which can be run on every parallel machine.