Direct synthesis of Zn(II) and Cu(II) coordination polymers based on 4,4′-bipyridine and 1,10-phenanthroline and evaluating their effects as catalyst on ammonium perchlorate thermal decomposition

Journal of Thermal Analysis and Calorimetry - Two coordination polymers (CPs) material, [Zn(μ-Cl)2(μ-bpy)]∞ (bpy?=?4,4′-bipyridine) and [Cu(bpy)(phen)(ClO4)2]n...     

Turbulent heat transfer in tubular heat exchangers with twisted tape

Journal of Thermal Analysis and Calorimetry - Enhancing heat transfer in heat exchangers has gained attention of researchers for many years because of reduction in costs of generating heat...     

Electrochemical Behavior and Determination of Hyoscine‐N‐Butylbromide from Pharmaceutical Preparations

The electrooxidation of hyoscine N‐butylbromide (HBB) was investigated by rotating disk electrode voltammetry, cyclic voltammetry and controlled potential coulometry in 0.1 M HNO₃ and in 0.1 M tetrabutylammonium perchlorate (TBAP) solutions of acetonitrile at a platinum (Pt) electrode. Based on the results obtained, it is suggested that a bromide ion of HBB was oxidized in one reversible step in aqueous solutions and in two reversible steps in acetonitrile. A differential pulse voltammetric (DPV) method at a Pt electrode was developed for the determination of HBB in the concentration range of 1.0 × 10^?6‐1.0 × 10^?3 M. The procedure was applied to the determination of HBB in its formulations as well as its recovery from blood serum and urine samples.     

Potassium peroxydisulfate as an efficient oxidizing agent for conversion of ethyl 3,4-dihydropyrimidin-2(1H)-one-5-carboxylates to their corresponding ethyl pyrimidin-2(1H)-one-5-carboxylates

Various ethyl 3,4-dihydropyrimidin-2(1H)-one-5-carboxylates were oxidized to their corresponding ethyl pyrimidin-2(1H)- one-5-carboxylates by potassium peroxydisulfate in refluxing aqueous acetonitrile. The products were obtained in good to excellent yields. The effect of the nature of 4-substituent and also the nature of solvent play an important role on the rate of oxidation.     

p‐TSA Catalyzed Synthesis of 2,4,5‐Triarylimidazoles from Ammonium Heptamolybdate Tetrahydrate in TBAI

A one‐pot synthesis of 2,4,5‐trisubstituted imidazoles from 1,2‐diketone or α‐hydroxy ketone, aldehyde and ammonium heptamolybdate tetrahydrate in an inexpensive and readily available ionic liquid, tetrabutylammonium iodide (TBAI) in molten state using catalytic amounts of p‐TSA has been described.     

Highly efficient polymer‐stabilized palladium heterogeneous catalyst: Synthesis,characterization and application for Suzuki–Miyaura and Mizoroki–Heck coupling reactions

A suitable approach to stabilize palladium nanoparticles (Pd NPs), with an average diameter of 3–4 nm, on magnetic polymer is described. A new magnetic polymer containing 4′‐(4‐hydroxyphenyl)‐2,2′:6′,2″‐terpyridine (HPTPy) ligand was prepared by the polymerization of itaconic acid (ITC) as a monomer and trimethylolpropane triacrylate (TMPTA) as a cross‐linker and fully characterized. Pd NPs embedded on the magnetic polymer were successfully applied in Suzuki–Miyaura and Mizoroki–Heck coupling reactions under low palladium loading conditions, and provided the corresponding products with excellent yields (up to 98%) and high catalytic activities (TOF up to 257 hr^?1). Also, the catalyst can be easily separated and reused for at least consecutive five times with a small drop in catalytic activity.     

Turbulent heat transfer and fluid flow of alumina nanofluid inside three-lobed twisted tube

Turbulent flow characteristics and heat transfer applications of a twisted heat exchanger with 3-lobed cross section along with Y-tape insert are numerically studied. The working fluids for the simulations are pure water and water–Al₂O₃ nanofluid using two-phase mixture model. The study is carried out for various nanofluid volume fractions of 0.01, 0.02 and 0.03 with Reynolds number in the range of 5000–20,000. The effect of nanoparticles in heat transfer augmentation for smooth and lobed tubes is discussed based on presenting the highest thermal performance, which is a relation between heat transfer rate and pressure loss. Results show that implementing the twisted tube with Y-tape insert enhances the heat transfer more than the twisted tube. Relative Nusselt numbers for twisted tubes decrease with Reynolds number in comparison with the plain tube. Turbulent intensity, swirl number and tangential velocity of twisted tube with insert are higher than empty twisted tube indicating that inserting the Y-tape intensifies the turbulence and disturbs the fluid flow further. On the other hand, although the twisted tube increases the pressure drop more than plain tube, the case with Y-tape drastically increases the friction factor. So, the thermal performance of twisted tube with insert is lower than empty twisted tube. Adding nanoparticles to the base fluid has different influence on the investigated cases. It augments the relative Nusselt number inside plain tube and empty twisted tube with slight increment in friction factor. Increasing the nanoparticles concentration enhances the heat transfer rates for these cases while it does not increase the relative Nusselt number inside twisted tube with Y-tape insert at high Reynolds number and nanoparticle concentration. Moreover, it can be found that twisted tube with or without Y-tape insert is more efficient at low Reynolds number in comparison with the plain tube.

     

A new strategy to design a graphene oxide supported palladium complex as a new heterogeneous nanocatalyst and application in carbon–carbon and carbon‐heteroatom cross‐coupling reactions

The palladium nanoparticles were successfully stabilized with an average diameter of 6–7 nm through the coordination of palladium and terpyridine‐based ligands grafted on graphene oxide surface. The graphene oxide supported palladium nanoparticles were thoroughly characterized and applied as an efficient heterogeneous catalyst in carbon–carbon (Suzuki‐Miyaura, Mizoroki‐Heck coupling reactions) and carbon–heteroatom (C‐N and C‐O) bond‐forming reactions. The catalyst was simply recycled from the reaction mixture and was reused consecutive four times with small drop in catalytic activity.