Extraction of polymer stress–strain behavior in the presence of self‐heating by the use of a simple model for the elastic–plastic deformation

Polymer materials are well known to be sensitive to strain rate and temperature. Self‐heating and friction effects also play an important role in the mechanical response of these materials. Numerous constitutive laws and phenomenological models have been developed to take into account these dependencies. This article proposes a simplified phenomenological model based on a mapping technique for the strain rate and temperature dependence. The effects of friction and adiabatic heating are also analyzed in this work. Relatively good results are obtained compared to experimental results for polypropylene and polychlorotrifluoroethylene. A parametric investigation of the effects of the interfacial equivalent stress (between the specimen and the compressive bars) and the fraction of plastic work converted into heat was performed. This parametric study allowed for a good approximation of these two parameters for the two studied polymers. POLYM. ENG. SCI., 55:2474–2481, 2015. © 2015 Society of Plastics Engineers     

Reinforcement of graphene nanoplatelets on plasticized poly(lactic acid) nanocomposites: Mechanical,thermal, morphology,and antibacterial properties

Plasticized poly(lactic acid) (PLA)‐based nanocomposites filled with graphene nanoplatelets (xGnP) and containing poly(ethylene glycol) (PEG) and epoxidized palm oil (EPO) with ratio 2 : 1 (2P : 1E) as hybrid plasticizer were prepared by melt blending method. The key objective is to take advantage of plasticization to increase the material ductility while preserving valuable stiffness, strength, and toughness via addition of xGnP. The tensile modulus of PLA/2P : 1E/0.1 wt % xGnP was substantially improved (30%) with strength and elasticity maintained, as compared to plasticized PLA. TGA analysis revealed that the xGnP was capable of acting as barrier to reduce thermal diffusion across the plasticized PLA matrix, and thus enhanced thermal stability of the plasticized PLA. Incorporation of xGnP also enhanced antimicrobial activity of nanocomposites toward Escherichia coli, Salmonella typhimurium, Staphylococcus aureus, and Listeria monocytogenes. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41652.     

Performance of PAM/PEI gel system for water shut‐off in high temperature reservoirs: Laboratory study

A polymer gel is one of the common remediate methods to either reduce or totally block excessive water production in oilfields. Some systems demonstrated an excellent performance in treating the problem like polyacrylamide tert‐butyl acrylate (PAtBA)/polyethylenimine (PEI). In this study, polyacrylamide (PAM) was introduced as a cheap alternative to PAtBA that can tolerate high salinity reservoirs. The thermal stability of the PAM/PEI polymeric gel in saline water was examined at 150°C (302F). Samples prepared in sea water showed better stability compared with distilled and field water. Dynamic rheology and core‐flooding experiments were used to evaluate the PAM / PEI gel system at high temperatures. NaCl and NH₄Cl were evaluated as a possible retarders for delaying the gelation time in order to achieve a successful placement. NH₄Cl was found to be more effective retarder. Core‐flooding tests were conducted in sandstone and carbonate cores. The subject polymer gel was injected at rates typical of those in field applications. The injectivity of PAM/PEI was tested in Berea sandstone cores with initial permeability of ～45 mD. The post‐treatment of the system showed a permeability reduction of ～94% for a period of two weeks. The injectivity in low permeability carbonate cores required more retardation compared with the injectivity in sandstone cores. The gel reduced the permeability to brine in Indiana limestone core by 99.8% for more than 5 months. Rheology of cured gel samples indicated that the gel strength needs about one day of curing in the core for the strength to stabilize. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41869.     

Synthesis,Characterization and Immunological Evaluation of Self‐Adjuvanting Group A Streptococcal Vaccine Candidates Bearing Various Lipidic Adjuvanting Moieties

Four group A streptococcal glycolipopeptide vaccine candidates with different lipidic adjuvanting moieties were prepared and characterized. The immunogenicity of the compounds was evaluated by macrophage and dendritic cell uptake studies and by in vivo quantification of systemic IgG antibody by ELISA. Three of the candidates showed significant induction of the IgG response.     

Microwave-assisted synthesis of isosorbide-derived diols for the preparation of thermally stable thermoplastic polyurethane

In order to prepare thermally stable isosorbide-derived thermoplastic polyurethane, the synthesis of two new chiral exo–exo configured diols, prepared from isosorbide, and two types of diphenols (bisphenol A and thiodiphenol) was described. The synthesis conditions were optimized under conventional heating and microwave irradiations. To prove their suitability in polymerization, these monomers were successfully polymerized using 4,4′-diphenylmethane diisocyanate (MDI) and hexamethylene diisocyanate (HDI). Both monomers and polymers have been studied by NMR, FT-IR, TGA, DSC; intrinsic viscosity of polymers has also been determined. The results showed the effectiveness of the synthetic strategy proposed; moreover, a dramatic reduction of the reaction time and an important improvement of the monomers yield using microwave irradiation have been demonstrated. The monomers, as well as the polymers, showed excellent thermal stability both in air and nitrogen. It was also shown that the introduction of sulphur in the polyurethane backbone was effective in delaying the onset of degradation as well as the degradation rate.     

Synthesis,characterization and controlled release properties of zinc–aluminium-beta-naphthoxyacetate nanocomposite

An organic–inorganic nanohybrid nanocomposite was synthesized by co-precipitation method using beta-naphthoxyacetate (BNOA) as guest anion and zinc–aluminium layered double hydroxide (Zn–Al-LDH) as the inorganic host. A well-ordered nanohybrid nanocomposite was formed when the concentration of BNOA was 0.08 M and the molar ratio of Zn to Al, R = 2. Basal spacing of layered double hydroxide containing nitrate ions expanded from 8.9 to 19.5 Å in resulting of Zn–Al-BNOA nanocomposite was obtained indicates that beta-naphthoxyacetate was successfully intercalated into interlayer spaces of layered double hydroxide. It was also found out the BET surface area increased from 1.13 to 42.79 m² g^?1 for Zn–Al-LDH and Zn–Al-BNOA nanocomposite, respectively. The BJH average pore diameter of the synthesized nanocomposite is 199 Å which shows mesoporous-type of material. CHNS analysis shows the Zn–Al-BNOA nanocomposite material contains 36.2 % (w/w) of BNOA calculated based on the percentage of carbon in the sample. Release of BNOA from the lamella of Zn–Al-BNOA was controlled by the zeroth and first order kinetics at the beginning of the deintercalation process up to 200 min and controlled by pseudo-second order kinetics for the whole process. This study suggests that layered double hydroxide can be used as a carrier for organic acid herbicide controlled release formulation of BNOA.     

Effects of water vapor on the oxidation and the fracture strength of SiC layer in TRISO fuel particles

Steam oxidation of silicon carbide (SiC) layer in nuclear fuel particles were performed in flowing argon‐water vapor mixture with a total pressure of 1 bar at 1173‐1673 K. Both the phase composition and the microstructure of the oxide scale on the SiC layer varied with the oxidation temperature. Reaction rates of water vapor with the SiC layer were determined by measuring the oxide scale thickness. It was found that the oxidation of SiC layer follows the parabolic law. The activation energy was calculated to be 103±11 kJ/mol. It is proposed that the rate determine step of the oxidation is the diffusion of water vapor molecules in the oxide scale. The fracture strength of SiC shell after steam oxidation was evaluated using a crush test. The fracture strength decreased with the increase in the oxidation temperature due to the thinning of the SiC layer.