Effect of iron on microstructure and mechanical properties of primary AlSi7Mg0.3 alloy

Effect of Fe on microstructure and mechanical properties of the primary AlSi7Mg0.3 alloy and the potential of Mn addition to counteract any adverse effects was investigated in the present work. The primary AlSi7Mg0.3 is a better alloy than its counterpart with twice as much Fe. β platelets grow twice as big when the Fe concentration is doubled. This, in turn, increases shrinkage porosity and leads to a 3-fold decrease in the tensile elongation values. Adding an equal amount of Mn helps to modify the β platelets into more compact α particles and also reduces shrinkage porosity. While these structural changes are reflected by a modest improvement in the mechanical properties, Mn addition fails to offer a full recovery in the ductility of the AlSi7Mg0.3 alloy. Hence, limiting the Fe content of the primary AlSi7Mg0.3 alloy to 0.12 wt% is worthwhile and pays off with superior microstructural features and mechanical properties.     

Synthesis and electrochemical properties of binary MgTi and ternary MgTiX (X = Ni,Si) hydrogen storage alloys

Mg-based hydrogen storage alloys are promising candidates for many hydrogen storage applications because of the high gravimetric hydrogen storage capacity and favourable (de)hydrogenation kinetics. In the present study we have investigated the synthesis and electrochemical hydrogen storage properties of metastable binary Mg_yTi_1?y (y = 0.80–0.60) and ternary Mg_0.63Ti_0.27X_0.10 (X = Ni and Si) alloys. The preparation of crystalline, single-phase, materials has been accomplished by means of mechanical alloying under controlled atmospheric conditions. Electrodes made of ball-milled Mg_0.80Ti_0.20 powders show a reduced hydrogen storage capacity in comparison to thin films with the same composition. Interestingly, for a Ti content lower than 30 at.% the reversible storage capacity increases with increasing Ti content to reach a maximum at Mg_0.70Ti_0.30. The charge transfer coefficients (α) and the rate constants (K₁ and K₂) of the electrochemical (de)hydrogenation reaction have been obtained, using a theoretical model relating the equilibrium hydrogen pressure, electrochemically determined by Galvanostatic Intermittent Titration Technique (GITT), and the exchange current. The simulation results reveal improved values for Mg_0.65Ti_0.35 compared to those of Mg_0.80Ti_0.20. The addition of Ni even more positively affects the hydrogenation kinetics as is evident from the increase in exchange current and, consequently, the significant overpotential decrease.     

Characterization of the polymer of a dipyrrolyl monomer by pyrolysis mass spectrometry

In this work, characterization of a homopolymer of succinic acid bis(4‐pyrrol‐1‐ylphenyl) ester prepared by galvonastatic polymerization was carried out by direct pyrolysis mass spectrometry. Although decomposition of the monomer yielding mainly butadionic acid and pyrrole occurred under the galvonastatic polymerization conditions, growth of the polymer through the pyrrole moieties was also achieved, yielding a ladder‐type polymer film. The polypyrrole chains contained both quinoid and aromatic units as in the case of polypyrrole, yet the extent of network structure was significantly diminished. A three‐step mechanism is proposed for the thermal decomposition process. The first step involves the cleavage of C₄H₄NC₆H₄O end groups. In the second step, decomposition of phenyl ester units and polypyrrole chains having quinoid structure takes place. The final stage of thermal degradation was attributed to decomposition of polypyrrole chains having aromatic structure. Copyright © 2004 Society of Chemical Industry     

Improvement of mechanical,thermal and antimicrobial properties of organically modified montmorillonite loaded polycaprolactone for food packaging

The aim of this study is to evaluate the biodegradable packaging materials which will be an alternative to traditional synthetic packaging materials. For this purpose, packaging films containing polycaprolactone (PCL), montmorillonite (MMT), and organically modified montmorillonite (OMMT) were prepared by solution casting method, and the mechanical, physical, structural, antimicrobial, and antifungal properties of these films were examined. Cetyl trimethyl ammonium bromide (CTAB) was used for the modification of montmorillonite. The structural properties of the prepared films were characterized by attenuated total reflection-Fourier transform infrared, X-ray powder diffraction, thermogravimetric analysis, and scanning electron microscopy. The PCL/OMMT structure was found to be thermally more stable than the PCL/MMT structure. The addition of OMMT to PCL improved the thermal and mechanical properties of the films compared with the pure PCL and PCL/MMT films. In addition, adding MMT/OMMT to the PCL caused an increase in the hardness of the films. In the antimicrobial analysis, while no inhibition effect was observed in PCL/MMT films, PCL/OMMT films showed inhibition effect against Staphylococcus aureus. Antifungal tests performed with the prepared films showed that the film-wrapped bread did not deteriorate for 40 days. It is thought that PCL/MMT and PCL/OMMT films prepared in this study will provide an advantage in applications as packaging material.     

Effects of hetero-armed star-shaped PCL-PLA polymers with POSS core on thermal,mechanical, and morphological properties of PLA

In this study, AB type-heteroarm star-shaped poly(ε-caprolactone)-poly(lactic acid) (PCL-PLA) polymers with polyhedral oligomeric silsesquioxane (POSS) core ((PCL)₄-POSS-(PLA)₄, coded as SPLA) were synthesized successfully by using ring opening polymerization and click chemistry techniques together. The synthesized polymers were compounded with commercial PLA at different blending ratios (PLA/SPLA = 100/0, 95/5, 90/10, and 80/20% wt). The effects of heteroarm SPLA polymers having different arm lengths (n = 10, 20, 30, and 50) on morphological, mechanical, and thermal behaviors of PLA were investigated. It is determined that SPLA polymers with four PLA and four PCL arms on its structure enhanced mechanical properties of PLA. The tensile modulus decreased, and lowest modulus values were observed with blends prepared at 80/20 ratio. Elongation at break values increased in all blends, maximum increment was observed with 1,4-phenylene diisocyanate (PDI) containing SPLA20 blends prepared at 90/10 ratio. This result showed that SPLA20 had optimum chain length for chain extension reactions of between PLA chains. Besides, a trade compatibilizer PDI was utilized to enhance the intercompatibility of binary polymer blends.