A simplified mathematical study of thermochemical preparation of particle oxide under counterflow configuration for use in biomedical applications

This study mathematically presents a counterflow non-premixed thermochemical technique for preparing a particle oxide used for cancer diagnosis and treatment. For this purpose, preheating, reaction, melting, and oxidation processes were simulated considering an asymptotic concept. Mass and energy conservation equations in dimensional and non-dimensional forms were solved using MATLAB^®. To preserve the continuity in the system and calculate the locations of melting and flame fronts, promising jump conditions were derived. In this research, variations in flame temperature, flame front location and mass fractions of the particle, particle oxide and oxidizer, with position, Lewis number and initial temperature of the particles were investigated. The simulation results were compared with those obtained from an earlier experimental study under the same conditions. Regarding the comparison, an appropriate compatibility was observed between the results. Based on the simulation results, flame temperature was found to be about 1310 K. Positions of flame and melting fronts were found to be ??1.8 mm and ??1.78 mm, respectively.

     

Analysis of unsteady mixed convection of Cu–water nanofluid in an oscillatory,lid-driven enclosure using lattice Boltzmann method

Journal of Thermal Analysis and Calorimetry - The unsteady physics of laminar mixed convection in a lid-driven enclosure filled with Cu–water nanofluid is numerically investigated. The top...     

Application of nitrogen-rich porous organic polymer for the solid-phase synthesis of 2-amino-4H-benzo[b]pyran scaffolds using ball milling process

Molecular Diversity - This paper presents the efficient synthesis of 2-amino-4H-benzo[b]pyrans using mesoporous poly-melamine-formaldehyde as a polymeric heterogeneous catalyst. According to the...     

New protocols for the synthesis of 5-amino-7-(4-phenyl)-4,7-dihydro-[1,2,4]triazolo[1,5-a]pyrimidine-6-carboxylate esters using an efficient additive

This work introduces a new additive named 4,4’-trimethylenedipiperidine for the practical and ecofriendly preparation of ethyl 5-amino-7-(4-phenyl)-4,7-dihydro-[1,2,4]triazolo[1,5-a]pyrimidine-6-carboxylate derivatives. This chemical is commercially available and easy to handle. It also possesses a low melting point and a broad liquid range temperature, high thermal stability, and good solubility in water. Based on green chemistry principles, the reaction was performed in a) a mixture of green solvents i.e. water and ethanol (1:1 v/v) at reflux temperature, and b) the additive was liquefied at 65 °C and the reaction was conducted in the liquid state of the additive. High yields of the desired triazolo-pyrimidines were obtained under both aforementioned conditions. Our results demonstrated that this additive, containing 2 Lewis base sites and able to act as an acceptor-donor hydrogen bonding group, is a novel and efficient alternative to piperidine, owing to its unique properties such as its reduced toxicity, nonflammable nature, nonvolatile state, broad liquid range temperature, high thermal stability, and ability to be safely handled. Furthermore, this additive could be completely recovered and exhibited high recyclability without any change in its chemical structure and no significant reduction in its activity. The current methodology has several advantages: (a) it avoids the use of hazardous materials, as well as toxic, volatile, and flammable solvents, (b) it does not entail tedious processes, harsh conditions, and the multistep preparation of catalysts, (c) it uses a metal-free and noncorrosive catalyst, and (d) reduces the generation of hazardous waste and simple work-up processes. The most important result of this study is that 4,4’-trimethylenedipiperidine can be a promising alternative for toxic, volatile, and flammable base reagents in organic synthesis owing to its unique properties.     

A novel magnetic nanocatalyst Fe3O4@PEG–Ni for the green synthesis of 2,3-dihydroquinazolin-4(1H)-ones

Ni-PEG (polyethylene glycol) complex supported on magnetic nanoparticle was created by grafting. The catalytic activity of Fe₃O₄@PEG–Ni was explored through one-pot green synthesis of 2,3-dihydroquinazolin-4(1H)-ones and used as an efficient and recoverable nanocatalyst. FT-IR, XRD, EDS, BET, TGA, VSM and SEM techniques were employed to specify the nanocatalyst. This heterogeneous nanocatalyst demonstrated acceptable recyclability and could be reused several times with no considerable loss of its catalytic activity.     

Effects of nanofluid and radiative heat transfer on the double-diffusive forced convection in microreactors

Journal of Thermal Analysis and Calorimetry - Understanding transport phenomena in microreactors remains challenging owing to the peculiar transfer features of microstructure devices and their...     

Synthesis of Bis‐spiro Cyclopropanes Based on Meldrum’s Acid by Milling

Reaction of 2,2‐dimethyl‐1,3‐dioxane‐4,6‐dione (Meldrum’s acid) with various solid aldehydes in the presence of cyanogen bromide and solid sodium ethoxide (EtONa) leads to the selective and efficient formation of bis‐spiro cyclopropanes based on Meldrum’s acid at the range of 0 °C to room temperature. The products were obtained in good to excellent yields. Structure elucidation is carried out by ¹H NMR, ¹³C NMR, FT‐IR spectroscopy, mass analyses and X‐ray crystallography techniques. A possible mechanism for the formation of products is also discussed under solvent‐free condition.     

Computational analysis of heat transfer augmentation and thermodynamic irreversibility of hybrid nanofluids in a tube fitted with classical and elliptical‑cut twisted tape inserts

Journal of Thermal Analysis and Calorimetry - This work investigates heat transfer and entropy generation of a turbulent flow of an Al2O3–Cu/water hybrid nanofluid in a plain tube (PT) with...