An in-Depth Analysis of the Swelling,Mechanical, Electrical,and Drug Release Properties of Agar–Gelatin Co-Hydrogels

Agar–gelatin-based co-hydrogels were prepared with different compositions of the agar and the gelatin fractions. The intermolecular hydrogen bonding was higher in the co-hydrogels as compared to the gelatin hydrogel. Swelling studies indicated diffusion-mediated swelling. The electrical stability of the co-hydrogels was higher as compared to the gelatin hydrogel. Though the firmness of the co-hydrogels was higher, Weichert model of viscoelasticity indicated that the inherent mechanical stability of the gelatin hydrogel was superior. The release of ciprofloxacin hydrochloride was predominately Fickian diffusion-mediated. In gist, the co-hydrogels can be tried as polymeric constructs for controlled drug delivery applications.     

Alginate‐gelatin blend with embedded voids for controlled release applications

Alginate gel is known for its potential use in the controlled release of drugs, and as a 3‐D structure for tissue harvesting. In this paper, the tuning of the performance of alginate gel by blending gelatin in the aqueous phase, and introducing bubbles in a regular alignment are discussed. Monodisperse bubbles in millimetre or submillimeter size were introduced into the aqueous suspension of the blend prior to gelation, using a novel fluidic arrangement. The CaCl₂ solution, added as the crosslinker diffused into the lamella, forming a rigid structure of calcium alginate. The effective blending of gelatin in alginate provided benefits of both the biopolymers in the final product. The benefits are the excellent absorption capacity of alginate and the mechanical strength of gelatin in the blend. The self‐aligned voids enabled further tuning of absorption capacity and/or rate of release. Also, the presence of voids enhanced the elastomeric quality of the composite structure. The uptake of Vitamin B₁₂ solution was measured gravimetrically, and the release in PBS buffer on a shaker was studied using UV‐vis spectrophotometer. For different loadings of void and gelatin, the absorption capacity, mechanical strength and the compression behavior were analysed. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44787.     

Formation polarity dependent improved resistive switching memory characteristics using nanoscale (1.3 nm) core-shell IrOx nano-dots

ABSTRACT: Improved resistive switching memory characteristics by controlling the formation polarity in an IrOx/Al2O3/IrOx-ND/Al2O3/WOx/W structure have been investigated. High density of 1 × 1013/cm2 and small size of 1.3 nm in diameter of the IrOx nano-dots (NDs) have been observed by high-resolution transmission electron microscopy. The IrOx-NDs, Al2O3, and WOx layers are confirmed by X-ray photo-electron spectroscopy. Capacitance-voltage hysteresis characteristics show higher charge-trapping density in the IrOx-ND memory as compared to the pure Al2O3 devices. This suggests that the IrOx-ND device has more defect sites than that of the pure Al2O3 devices. Stable resistive switching characteristics under positive formation polarity on the IrOx electrode are observed, and the conducting filament is controlled by oxygen ion migration toward the Al2O3/IrOx top electrode interface. The switching mechanism is explained schematically based on our resistive switching parameters. The resistive switching random access memory (ReRAM) devices under positive formation polarity have an applicable resistance ratio of > 10 after extrapolation of 10 years data retention at 85°C and a long read endurance of 105 cycles. A large memory size of > 60 Tbit/sq in. can be realized in future for ReRAM device application. This study is not only important for improving the resistive switching memory performance but also help design other nanoscale high-density nonvolatile memory in future.     

Isothermal crystallization kinetics of polypropylene in melt‐mixed composites of polypropylene and multi‐walled carbon nanotubes

The isothermal crystallization behaviour of the polypropylene (PP) phase in PP/multi‐walled carbon nanotubes (MWCNTs) composites has been investigated via differential scanning calorimetric analysis, which showed the influence of the varying dispersion level of MWCNTs in the respective PP matrix. PP/MWCNTs composites were prepared via melt‐blending technique, wherein two different grades of MWCNTs of varying average “agglomerate” size and varying entanglements (N‐MWCNTs and D‐MWCNTs) were utilized. Furthermore, the influence of melt‐viscosity of the PP phase was investigated on the crystallization kinetics of the PP/MWCNTs composites. Heterogeneous nucleation ability of MWCNTs has resulted in a decrease in half time of crystallization (t _1/2) from ～14 min for pure PP to ～6 min for PP/N‐MWCNTs and ～11 min for PP/D‐MWCNTs composites at 1 wt% of MWCNTs at 132 °C. Overall rate of crystallization (k) has significantly increased to 4.9 × 10^?2 min^?1 for PP/N‐MWCNTs composite as compared with 6.2 × 10^?3 min^?1 for PP/D‐MWCNTs composite at 0.5 wt% of MWCNTs at 132 °C. Moreover, the effect of a novel organic modifier, Li‐salt of 6‐amino hexanoic acid along with a compatibilizer (PP‐g‐MA) has also been investigated on the crystallization kinetics of the PP phase in PP/MWCNTs composites. POLYM. ENG. SCI., 57:1136–1146, 2017. © 2017 Society of Plastics Engineers     

Stripping and recycling of metal ions in aqueous nitric acid solutions: Experimental and molecular dynamics insights

Stripping of metal ions (i.e., Cs⁺ and Na⁺) in presence of ionophore such as dibenzo-18-crown-6, (DB18C6) from the ionic liquid phase to the aqueous nitric acid phase by molecular dynamics simulation is reported. The experimentally determined stripping percentages of Na⁺ (i.e., 43.4, 38.5, 34.4, and 31.9%) were found to be higher than the same for Cs⁺ (i.e., 32.6, 32.0, 31.3, and 30.2%). The nonbonded and the hydrogen bond energies between Na⁺ and water (i.e., −356.41 and −363.77 kcal/mol) were higher when compared with Cs⁺ (i.e., −212.43 and −221.04 kcal/mol). The spatial distribution functions further confirmed that the surfaces of Na⁺ were very closely distributed around the active sides of water whereas for Cs⁺, it was distributed very far from the water molecules. In the penultimate section, the effect of methanol to the aqueous phase was studied so as to enhance the extraction efficiency of the complex.     

Experimental evidence of concurrent compositional and structural instabilities leading to ω precipitation in titanium-molybdenum alloys

The ω phase is commonly observed in many commercial β or near-β titanium alloys on rapidly cooling from the single β phase field and also during subsequent isothermal annealing. However, the crystallographic formation mechanism for the ω particles is hitherto unclear/under discussion. The present study primarily focuses on ω precipitation within the β (body-centered cubic (bcc)) matrix of simple model binary titanium-molybdenum (Ti-Mo) alloys. It provides direct experimental evidence of the formation of ω-like embryos from competing compositional and structural instabilities arising in the bcc lattice of Ti-Mo alloys during rapid cooling from the high-temperature single β phase field. The displacive partial collapse of the {1 1 1} planes of the parent bcc structure within compositionally phase-separated regions containing several at.% less of Mo, forming ω-like embryos, has been conclusively shown by coupling aberration-corrected high-resolution scanning transmission electron microscopy with atom probe tomography observations. Growth and coarsening of these ω-like embryos take place during subsequent isothermal annealing, accompanied with both a completion of the collapse of the {1 1 1} β planes leading to a fully developed ω structure as well as rejection of Mo from these precipitates, resulting in near-equilibrium compositions.     

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.