Transport of cobalt(II) through a hollow fiber supported liquid membrane containing di-(2-ethylhexyl) phosphoric acid (D2EHPA) as the carrier

This work presents experimental, modeling and simulation studies for Co²⁺ ion extraction using hollow fiber supported liquid membrane (HFSLM) operated in a recycling mode. Extractant di-(2-ethylhexyl) phosphoric acid (D2EHPA) diluted with kerosene has been used as the membrane phase. The Co²⁺ ion concentration in the aqueous feed phase was varied in the range of 1–3 mM. Also, D2EHPA concentration was varied in the range of 10–30% (v/v). A mass transfer model has been developed considering the complexation and de-complexation reactions to be fast and at equilibrium. Equations for extractant mass balance and counter-ion (H⁺) transport have also been incorporated in the model. Extraction equilibrium constant (K_ex) for cobalt–D2EHPA system has been estimated from equilibration experiments and found to be 3.48 × 10⁻⁶. It was observed that the model results are in good agreement with the experimental data when diffusivity of metal-complex (D_m) through the membrane phase is 1.5 × 10⁻¹⁰ m²/s. Feed phase pH and strip phase acidity had negligible effect on the extraction profiles of Co²⁺ ions. An increase in D2EHPA concentration increased extraction rates of Co²⁺ ions. The membrane phase diffusion step was found to be the controlling resistance to mass transfer.     

A novel concept for improved thermal management of the planar SOFC

A new design for the solid oxide fuel cell (SOFC) planar stack is proposed to minimise the thermal gradients in the cell. This design involves including a secondary air channel with flow in the counter direction to the cathodic air channel. The effectiveness of the new design is tested by means of a tank in series reactor (TSR) model of the SOFC. It is found that the new design is capable of reducing the steady state temperature difference across the cell to less than 2 K over a range of voltages, while satisfying the requirements on fuel utilisation (FU) and cell average temperature. This is achieved by manipulating the primary air channel inlet flow rate and the secondary air channel inlet temperature. More modelling and experimental studies are required to further investigate the proposed design.     

Synthesis of alkyne‐terminated xanthate RAFT agents and their uses for the controlled radical polymerization of N‐vinylpyrrolidone and the synthesis of its block copolymer using click chemistry

Two new alkyne‐terminated xanthate reversible addition‐fragmentation chain‐transfer (RAFT) agents: (S)‐2‐(Propynyl propionate)‐(O‐ethyl xanthate) (X₃) and (S)‐2‐(Propynyl isobutyrate)‐(O‐ethyl xanthate) (X₄) were synthesized and characterized and used for the controlled radical polymerization of N‐vinylpyrrolidone (NVP). X₃ showed better chain transfer ability in the polymerization at 60°C. Molecular weight of the resulted polymer increased linearly with the increase in monomer loading. Kinetics study with X₃ showed the pseudo‐first order kinetics up to 67% monomer conversion. Molecular weight (M_n) of the resulting polymer increased linearly with the increase in the monomer conversion up to around 67%. With the increase in the monomer conversion, polydispersity of the corresponding poly(NVP)s initially decreased from 1.34 to 1.32 and then increased gradually to 1.58. Chain‐end analysis of the resulting polymer by ¹H‐NMR and FTIR showed clearly that polymerization started with radical forming out of xanthate RAFT agent. Living nature of the polymerization was also confirmed from the successful homo‐chain extension experiment and the hetero‐chain extension experiment involving synthesis of poly(NVP)‐b‐polystyrene amphiphilic diblock copolymer. Formed alkyne‐terminated poly(NVP) also allowed easy conjugation to azide‐terminated polystyrene by click chemistry to prepare well‐defined poly(NVP)‐b‐polystyrene block copolymers. Resulting polymers were characterized by GPC, ¹H‐NMR, FTIR, and thermal study. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Experiments on the induction welding of thermoplastics

In induction welding of thermoplastics, induction heating of a gasket, made of a ferromagnetic‐powder‐filled bonding material and placed at the interface of thermoplastic parts to be joined, is used to melt the interface; subsequent solidification of the melt results in a weld. Tensile tests on induction butt‐welds of polycarbonate (PC), poly(butylene terephthalate) (PBT), and polypropylene (PP) are used to characterize achievable weld strengths, and microscopy is used to correlate weld strength with the morphology of failure surfaces. In PC, PBT, and PP relative weld strengths as high as 48%, 43%, and 55% of the respective strengths of PC, PBT, and PP have been demonstrated. Relative weld strengths on the order of 20% have been demonstrated in PC‐to‐PBT welds.     

Comparison of vibration and hot‐tool thermoplastic weld morphologies

Because of very different heating rates in hot‐tool and vibration welding, and the higher weld pressures used in vibration welding inducing more squeeze flow, the weld zones in these two processes see very different flows and cooling rates, resulting in different morphologies. The weld morphologies of bisphenol‐A polycarbonate (PC) and poly(butylene terephthalate) (PBT) for these two processes are discussed in relation to these differences. The thickness of the heat‐affected zone (HAZ) in hot‐tool welds increases with the melt time; this zone is thicker than in vibration welds. The HAZ thickness in hot‐tool welds increases from the center toward the edges. The HAZ thickness is more uniform in vibration welds. Hot‐tool welds of PC have large numbers of bubbles around the central plane; the bubble size increases from the center to the edges. PC vibration welds do not have bubbles except near the edges. Both hot‐tool and vibration welds of PBT do not have bubbles. The morphology of the HAZ in PBT is very different in hot‐tool and vibration welds. In hot‐tool welds, the resolidified material consists of a sandwich structure in which two thin layers with very small crystallites surround a thicker central layer in which the spherulites are almost as large as in the original molded material. In vibration welds, the HAZ has large crystallinity gradients across the weld zone as well as squeeze‐flow induced distortion of the small spherulites.     

Effects of Substrate Orientation and Metal Film Thickness on the Intrinsic Strength, Intrinsic Fracture Energy, and Total Fracture Energy of Tantalum–Sapphire Interfaces

Parameters that characterize interface fracture are defined, and procedures to measure them are discussed. The interface strength σ_o is measured by using a novel laser spallation experiment, which uses a laser-induced stress wave to separate the interface. The intrinsic ( G _o) and total ( G _c) fracture energies are measured using a double cantilever beam experiment performed at ambient and cryogenic temperatures, respectively. These experiments are used to obtain relationships between G _c and G _o, and between σ_o and G _o, for interfaces between sputter-deposited polycrystalline Ta coatings and sapphire substrates. The intrinsic toughness and strength were modified by changing the orientation of the sapphire surface (basal and prismatic), while G _c was varied by changing the test temperature (ambient and cryogenic) and the thickness (1–3 μm) of the ductile Ta layer. Besides providing values that have interest in their own right, the work presented here provides a general framework for designing interfaces in bonded structures and serves as a basis to develop atomistic and continuum interface fracture models.     

Dry Sliding Tribological Behavior of Brake Oil Conditioned Ceramic Matrix Composites Reinforced With Carbon Fabric

Silicon - Ceramic composites are extremely sensitive to the surrounding environment. Their tribological performance may degrade drastically if they are polluted by some external agent. The present...     

1-[2-(1-Cyclobutylpiperidin-4-yloxy)-6,7-dihydro-4H-thiazolo[5,4-c]pyridin-5-yl]propan-1-one: a Histamine H3 Receptor Inverse Agonist with Efficacy in Animal Models of Cognition

A series of chemical optimizations, which was guided by in vitro affinity at histamine H₃ receptor (H₃R), modulation of lipophilicity, ADME properties and preclinical efficacy resulted in the identification of 1-[2-(1-cyclobutylpiperidin-4-yloxy)-6,7-dihydro-4H-thiazolo[5,4-c]pyridin-5-yl]propan-1-one ( 45 e ) as a potent and selective (K_i=4.0 nM) H₃R inverse agonist. Dipsogenia induced by (R)-α-methylhistamine was dose dependently antagonized by 45 e , confirming its functional antagonism at H₃R. It is devoid of hERG and phospholipidosis issues. Compound 45 e has adequate oral exposures and favorable half-life in both rats and dogs. It has demonstrated high receptor occupancy (ED₈₀=0.22 mg/kg) and robust efficacy in object recognition task and, dose dependently increased acetylcholine levels in brain. The sub-therapeutic doses of 45 e in combination with donepezil significantly increased acetylcholine levels. The potent affinity, selectivity, in vivo efficacy and drug like properties together with safety, warrant for further development of this molecule for potential treatment of cognitive disorders associated with Alzheimer's disease.     

A Review on Wear and Friction Performance of Carbon–Carbon Composites at High Temperature

Carbon–carbon (C/C) composite is one of the best ceramic matrix composite due to its high mechanical properties and applications at control environments in various sectors. Carbon–carbon composite is made of woven carbon fibers; carbonaceous polymers and hydrocarbons are used as matrix precursors. These composites generally have densities <2.0 g/cm³ even after densification. C/C composites have good frictional properties and thermal conductivity at high temperature. Also C/C composite can be used as brake pads in high‐speed vehicles. In spite of various applications, C/C composites are very much prone to oxidation at high temperature. Therefore, C/C composites must be protected from oxidation for the use at high temperature.