Study of bactericidal efficiency of magnetron sputtered TiO2 films deposited at varying oxygen partial pressure

TiO₂ thin films have been deposited at different Ar:O₂ gas ratios (20:80,70:30,50:50,and 40:60 in sccm) by rf reactive magnetron sputtering at a constant power of 200 W. The formation of TiO₂ was confirmed by X-ray photoelectron spectroscopy (XPS). The oxygen percentage in the films was found to increase with an increase in oxygen partial pressure during deposition. The oxygen content in the film was estimated from XPS measurement. Band gap of the films was calculated from the UV-Visible transmittance spectra. Increase in oxygen content in the films showed substantial increase in optical band gap from 2.8 eV to 3.78 eV. The Ar:O₂ gas ratio was found to affect the particle size of the films determined by a transmission electron microscope (TEM). The particle size was found to be varying between 10 and 25 nm. The bactericidal efficiency of the deposited films was investigated using Escherichia coli (E. coli) cells under 1 h UV irradiation. The growth of E. coli cells was estimated through the Optical Density measurement by UV-Visible absorbance spectra. The qualitative analysis of the bactericidal efficiency of the deposited films after UV irradiation was observed through SEM. A correlation between the optical band gap, particle size and bactericidal efficiency of the TiO₂ films at different argon:oxygen gas ratio has been studied.     

Effect of specimen thickness on the creep response of a Ni-based single-crystal superalloy

Creep tests on Ni-based single-crystal superalloy sheet specimens typically show greater creep strain rates and/or reduced strain or time to creep rupture for thinner specimens than predicted by current theories, which predict a size-independent creep strain rate and creep rupture strain. This size-dependent creep response is termed the thickness debit effect. To investigate the mechanism of the thickness debit effect, isothermal, constant nominal stress creep tests were performed on uncoated PWA1484 Ni-based single-crystal superalloy sheet specimens of thicknesses 3.18 and 0.51 mm under two test conditions: 760 °C/758 MPa and 982 °C/248 MPa. The specimens contained initial microvoids formed during the solidification and homogenization processes. The dependence of the creep response on specimen thickness differed under the two test conditions: at 760 °C/758 MPa there was a reduction in the creep strain and the time to rupture with decreasing section thickness, whereas at 982 °C/248 MPa a decreased thickness resulted in an increased creep rate even at low strain levels and a decreased time to rupture but with no systematic dependence of the creep strain to rupture on specimen thickness. For the specimens tested at 760 °C/758 MPa microscopic analyses revealed that the thick specimens exhibited a mixed failure mode of void growth and cleavage-like fracture while the predominant failure mode for the thin specimens was cleavage-like fracture. The creep specimens tested at 982 °C/248 MPa in air showed the development of surface oxides and a near-surface precipitate-free zone. Finite-element analysis revealed that the presence of the alumina layer at the free surface imposes a constraint that locally increases the stress triaxiality and changes the value of the Lode parameter (a measure of the third stress invariant). The surface cracks formed in the oxide scale were arrested by further oxidation; for a thickness of 3.18 mm the failure mode was void nucleation, growth and coalescence, whereas for a thickness of 0.51 mm there was a mixed mode of ductile and cleavage-like fracture.     

Laser-Deposited In Situ TiC-Reinforced Nickel Matrix Composites: 3D Microstructure and Tribological Properties

A new class of Ni-Ti-C-based metal-matrix composites has been developed using the laser-engineered net shaping? process. These composites consist of an in situ formed and homogeneously distributed titanium carbide (TiC) phase reinforcing the nickel matrix. Additionally, by tailoring the Ti/C ratio in these composites, an additional graphitic phase can also be engineered into the microstructure. Serial-sectioning, followed by three-dimensional reconstruction of the microstructure in these composites, reveals homogeneously distributed primary and eutectic titanium carbide precipitates as well as a graphitic phase encompassing the primary carbides within the nickel matrix. The morphology and spatial distribution of these phases in three dimensions reveals that the eutectic carbides form a network linked by primary carbides or graphitic nodules at the nodes, which suggests interesting insights into the sequence of phase evolution. These three-phase Ni-TiC-C composites exhibit excellent tribological properties, in terms of an extremely low coefficient of friction while maintaining a relatively high hardness.     

Integrated Computational Materials Engineering (ICME) Approach to Design of Novel Microstructures for Ti-Alloys

In this overview, we present integrated CAPHAD and phase-field modeling with critical experiments to explore a newly discovered, nonconventional, solid–solid phase transformation pathway based on the so-called pseudo-spinodal mechanism. We show that this new transformation pathway offers a new design strategy for Ti alloys with extremely fine and uniform α + β microstructures that could potentially have highly attractive balances of mechanical properties. To broaden the processing window for such a mechanism to operate, we also explore a different nonconventional transformation pathway that involves precursory phase separation. In addition, the variant selection process during the β → α transformation leading to macrozones is investigated and the results could shed light on how to control processing conditions to avoid or reduce microtexture at both the individual β grain level and the overall polycrystalline sample level.     

Modeling of heat transfer in rotational molding

Rotational molding is a process for manufacturing hollow or open‐sided plastic products using a rotating mold subjected to heating and then cooling. The process is attractive for the production of stress‐free objects at a competitive cost. In this article, a modified model for heat transfer in rotational molding is proposed, which assumes that the heat transfer at the mold‐powder interface is because of convection, whereas the powder particles are heated up by conduction. Heat transfer through the mold–air contact is also included. A source‐based formulation is used for modeling the layer‐by‐layer nonisothermal deposition of plastic. The reduced heat transfer due to warpage is calculated by using a modified heat transfer coefficient. Good overall agreement is found between the cycle times as predicted by the model and the experimental data. The model is then used for calculating the cycle time for particulate composites, based on their effective properties. A reduction in the cycle time is observed in the case of reinforced composites. This is attributed to the increase in thermal conductivity of the particulate composites and the reduced mass fraction of the polymer. Numerical calculations of the cycle time for the glass‐bead reinforced composites are found to be in good agreement with the experimental results. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers     

Short jute fiber‐reinforced polypropylene composites: Dynamic mechanical study

Short jute fiber‐reinforced polypropylene (PP) composites were prepared using a high‐speed thermokinetic mixer. A compatibilizer was used to improve the molecular interaction between jute and PP. Both the percent weight fraction of the jute fiber and compatibilizer were varied to study the dynamic mechanical thermal (DMT) properties. Dynamic parameters such as storage flexural modulus (E′), loss flexural modulus (E″), storage shear modulus (G′), loss shear modulus (G″), and loss factor or damping efficiency (tan δ) were determined in a resonant frequency mode. The transition peak nature, amplitude, and temperature of E′, E″, G′, G″, and tan δ of different compositions were shown to indicate possible improvements of molecular interaction in the presence of a compatibilizer. The modulus retention term, a plot of the reduced modulus with the weight fraction of the jute fiber, also indicate its improvement. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 531–539, 1999     

Photograft copolymerization of methyl methacrylate on silk fiber using titanium(III) chloride–potassium persulphate redox initiator in a limited aqueous system. I

Graft copolymerization of methyl methacrylate (MMA) onto mulberry silk fibers has been investigated in a limited aqueous system employing titanium(III) chloride–K₂S₂O₈ as the redox initiator under a photoactive condition with visible light. Polymerization in the presence of light at 32 ± 1°C has been found to be more pronounced than in the dark under identical conditions. The percentage of grafting, the percentage of total conversion, and the percentage of grafting efficiency have been studied by varying the reaction time, concentration of monomer, initiator concentration, solvent composition, and pH of the medium. A high percentage of grafting (∼ 93%), high grafting efficiency (∼ 97%), and the percentage of total conversion (∼ 25%) have been obtained with little homopolymer formation. Characterization of the grafted fibers has been investigated by Fourier transform infrared spectroscopy and scanning electron microscopy. Finally, the reaction mechanism has been discussed by considering hydrogen bonding. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 73: 2187–2193, 1999     

An XPS Study with Depth Profiling for the Surface Oxide Layer Formed on Aluminides Produced on Superalloy 690 Substrates

Superalloy 690 substrates containing mainly Cr and Ni aluminides on the uppermost surface, formed by atmospheric plasma spraying and heat treatment, were oxidized at 1273 K in air for 2 h. Quantitative X-ray photoelectron spectroscopy (XPS) analyses indicated that the outermost surface layer formed on aluminides is composed of ~ 21.0 at.% Al⁺³ (as Al₂O₃), 17.0 at.% Al⁰ (elemental aluminium), 1.4 at.% Cr⁺³ (as Cr₂O₃) and 60.5 at.% O (in Al₂O₃ and Cr₂O₃ and also includes oxygen contaminant). Surface sputtering for 5 min exhibited splitting of Cr2p_3/2 peak into a doublet comprising Cr⁺³ (0.9 at.%) and Cr⁰ (0.4 at.%) with the presence of 1.15 at.% Ni⁰ in the surface layer that mainly contained ~ 37.3 at.% Al⁺³, 7.3 at.% Al⁰ and 52.9 at.% O. Surface sputtering for 15 min indicated surface composition similar to surface sputtered for 5 min but with a marked reduction in ratio of Al⁺³/Al⁰ (32.2 at.% Al⁺³/11.90 at.% Al⁰) in the surface layer.     

Room temperature living cationic polymerization of styrene with HX-styrenic monomer adduct/FeCl3 systems in the presence of tetrabutylammonium halide and tetraalkylphosphonium bromide salts

Living cationic polymerization of styrene was achieved with a series of initiating systems consisting of a HX-styrenic monomer adduct (X = Br, Cl) and ferric chloride (FeCl₃) in conjunction with added salts such as tetrabutylammonium halides (nBu₄N⁺Y⁻; Y⁻ = Br⁻, Cl⁻, I⁻) or tetraalkylphosphonium bromides [nR′₄PBr; R′ = CH₃CH₂-, CH₃(CH₂)₂CH₂-, CH₃(CH₂)₆CH₂-] or tetraphenylphosphonium bromide [(C₆H₅)₄PBr] in dichloromethane (CH₂Cl₂) and in toluene. Comparison of the molecular weight distributions (MWDs) of the polystyrenes prepared at different temperatures (e.g., −25 °C, 0 °C and 25 °C) showed that the polymerization is better controlled at ambient temperature (25 °C). The polymerization was almost instantaneous (completed within 1 min) and quantitative (yield ∼100%) in CH₂Cl₂. In CH₂Cl₂, polystyrenes with moderately narrow (M_w/M_n ∼ 1.33-1.40) and broad (M_w/M_n ∼ 1.5-2.4) MWDs were obtained respectively with and without nBu₄N⁺Y⁻. However, in toluene, the MWDs of the polystyrenes obtained respectively with and without nBu₄N⁺Y⁻/nR′₄P⁺Br⁻ were moderately narrow (M_w/M_n = 1.33-1.5) and extremely narrow (M_w/M_n = 1.05-1.17). Livingness of this polymerization in CH₂Cl₂ was confirmed via monomer-addition experiment as well as from the study of molecular weights of obtained polystyrenes prepared simply by varying monomer to initiator ratio. A possible mechanistic pathway for this polymerization was suggested based on the results of the ¹H NMR spectroscopic analysis of the model reactions as well as the end group analysis of the obtained polymer.     

Investing in recovering water for the environment in Australia's Murray-Darling Basin

Irrigated agriculture makes an important contribution to the economy of Australia's Murray-Darling Basin. Competing water demand, recurring drought and climate change have ushered in an era of water policy reform. To recover water for the environment, surface water extraction is capped and investment in irrigation infrastructure is prioritized. This article applies a computable general equilibrium model to evaluate the economic impacts of investment in irrigation in a case study of the Murrumbidgee subcatchment. Results indicate an increase in regional output, income and employment, while at the national level there is a small negative impact resulting from the transfer of resources to the basin and the crowding out of private investment.