Volume 23 (2021): Issue 2 (June 2021)

Zero-dimensional two-stage SOFC stacks dynamic model was developed to investigate the effect of operating parameters on stacks performance. The model resolves spatially thermal and thermo-electrochemical behaviour for electrochemical reactions, Catalytic Partial Oxidation and Steam Reforming processes. Design variables and thermo-electrochemical properties were obtained from in-house-fabricated SOFCs carried out by project partners. The completed SOFCs based Combined Heat and Power, CHP, system model was validated by data¹⁸ and numerical results obtained at steady-state mode showing its high-fidelity. A parametric study with respect to key operating parameters including changes in fuel utilization, lambda number and current density values was conducted. The global CHP system dynamic response, in term of the current/voltage delivered by two-stage SOFC stacks, under a fixed fuel utilization, has been determined resulting in greater variations in the voltage of a single cell in the first stack in comparison to the corresponding values in the second stack.

To make clear the feasibility and influence factors of diesel fuel autothermal reforming to hydrogen, PdCeCr- FeCu/Al₂O₃ catalyst was prepared by equivalent-volume impregnation method. Experimental facility based on an adiabatic tubular reactor with preheating section was designed and set up, the behaviors of diesel reforming to hydrogen with straight-run diesel as a raw material according to the analysis of the components were studied. Diesel oil reforming over a catalyst for hydrogen production was analyzed using an adiabatic tubular reactor with a preheating section that was designed and built in-house. The operating conditions were optimized. Under the suitable operating conditions, viz., catalyst bed inlet temperature of 700 °C, diesel liquid space velocity of 0.24 h⁻¹, water-carbon ratio of 20, and oxygen-carbon ratio of 0.6, the hydrogen yield reached 28.3 (mol/mol).

Residual anionic polyacrylamide in polymer-flooding oil production wastewater results in the formation of a thermodynamically stable system. In this study, the effects of three different types of medicaments, namely, cationic, anionic and nonionic agents, in dynamic treatments, such as adding a position, dosage and combined processes of chemical addition, on the oil removal rate of sewage were examined. In the treatment with a single agent, the oil removal rate of the cationic agent CQY-1 and the nonionic agent CHF-2 was ≥ 97.8%. The charge characteristics of different ionic agents for the combined dosing treatment indicated that the oil removal rate was better than that of a single agent; the combined dosing ratio was 50 mg/L CHP-1 and 50 mg/L CHP-2. At 80 mg/L CQY-1, the oil removal rate of the dynamic process was ≥ 98.8%, and the dosage of CQY-1 was reduced from 200 mg/L to 50–150 mg/L, which corresponded to a decrease of 25.0%–75.0%. Therefore, the combined dosing process effectively reduced the single dosage.

Coumarin and its nitrogen analogue 1-aza coumarin are a class of lactones and lactams, respectively, which are indispensable heterocyclic units to both chemists and biochemists. 1-Aza coumarin derivatives, which ultimately metabolize as the corresponding 8-hydroxy coumarins in the biological system are therefore found to be very good anti-inflammatory, anti-cancer, and analgesic agents. A series of hybrid substituted coumarin and azacoumarin-3-carboxylic acid derivatives (8-methoxycoumarin-3-carboxylic acid (4a), 8-methoxyazacoumarin-3-carboxylic acid (4b), 5-bromo-8-methoxycoumarin-3-carboxylic acid (5a), 5-bromo-8-methoxyazacoumarin-3-carboxylic acid (5b), 2-acetoxy-5-bromo-8-methoxyquinoline-3-carboxylic acid (6), and 5,7-di(phenylazo)-8-methoxycoumarin-3-carboxylic acid (7) were synthesized and structurally proved using spectral and elemental analysis data. Substituted coumarin-3-carboxylic acid (4a and 5a) and Substituted azacoumarin-3-carboxylic acid (4b, 5b and 6) were tested for their in vitro cytotoxic activity against MCF-7 and HepG-2 cell lines.

In this study, the effects of the lacquer applied to the printing materials which were printed by electrophotographic printing method on printing quality were investigated. In practice, printing materials with the same weight and different optical properties were used and the study was carried out in three stages. The optical and physical properties of the printing materials used in the first part were determined, in the second part, the printing of these materials by electrophotographic printing method and printability tests were performed. In the third chapter, matte and glossy lacquers were applied to these printed materials and printability tests were repeated. As a result of the study, it was observed that the application of gloss and matte lacquer caused a decrease in the printing density values and also the application of matte lacquer caused a decrease in the gloss values.

Untreated coking effluent presents a great challenge for sustainable development of the steel industry and environment preservation. In this study, an internal micro-electrolysis method using Fe/C materials was employed for pretreatment of real coking wastewater with high mass concentration. The Fe/C materials were prepared by Fe powder and graphite powder; and the characteristics of surface morphology, structure, composition of the synthesized materials were examined by Scanning electron microscopy (SEM), X-ray diffraction (XRD) and Energy Dispersive X-ray Spectroscopy (EDS). The effects of factors namely dosage of Fe/C material, treatment time, initial pH and temperature were investigated via chemical oxygen demand (COD) and phenol removal efficiencies. Optimal treatment efficiency was attained at pH of 4, Fe/C dosage of 40 g/L, treatment time of 360 minutes and temperature of 25°C. After the internal electrolysis process, the values of COD, BOD5, and phenol of the wastewater were 6500, 4850 and 0.1 mg/L, respectively.

The main interest now is the development of metallic or inorganic-organic compounds to prepare nanoparticle materials. The use of new compounds could be beneficial and open a new method for preparing nanomaterials to control the size, shape, and size of the nanocrystals. In this article, the thermal decomposition of [M₂(o-tol)₂(H₂O)₈] Cl₄ (where o-tol is ortho-tolidine compound, M = Ni²⁺, Co²⁺, Cu²⁺) new precursor complex was discussed in solid-state conditions. The thermal decomposition route showed that the synthesized three complexes were easily decomposed into NiO, Co₃O₄ and CuO nanoparticles. This decomposition was performed at low temperatures (~600°C) in atmospheric air without using any expensive and toxic solvent or complicated equipment. The obtained product was identified by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), transmission electron microscopy (TEM) and energy-dispersive X-ray spectroscopy (EDX). FT-IR, XRD and EDX analyses revealed that the NiO nanoparticles exhibit a face-centered-cubic lattice structure with a crystallite size of 9–12 nm. The formation of a highly pure spinel-type Co₃O₄ phase with cubic structure showed that the Co₃O₄ nanoparticles have a sphere-like morphology with an average size of 8–10 nm. The XRD patterns of the CuO confirmed that the monoclinic phase with the average diameter of the spherical nanoparticles was approximately 9–15 nm.

Co(II), Ni(II) and Cu(II) decxycholate complexes are interesting due to their biologically active and deliberate interest in the research due to their coordination properties. The microanalytical ‘elemental analysis’, molar conductivity, (infrared and Raman) spectroscopy, thermal analyses (TGA/DSC), UV-vis spectra, and ESR for copper(II) decxycholate complex investigations were performed in the structural assignments of Co(II), Ni(II) and Cu(II) decxycholate complexes. Reaction of the sodium deoxycholate ligand (C₂₄H₃₉O₄Na) with three transition metal ions form the complexes of formulae, [M(C₂₄H₃₉O₄)₂(H₂O)₂]. xH₂O where M = Co(II), Ni(II) and Cu(II) where x = 2 for Cu(II) and x = 4 in case of M = Co(II) or Ni(II) metal ions. The FTIR spectra of the complexes show that decxycholate molecule is present as bidentate ligand. Molecular docking utilizing to additionally examine the interaction of COVID-19 (6LU7) with different complexes of deoxycholic acid with Co(II), Ni(II) and Cu(II). Furthermore, in the case of Co(II) deoxycholate complex, the probe is surrounded by amino residues Met235, Pro241, Glu240, Pro108, Gln110, Phe294, and Ile152. The probe molecule of Ni(II) deoxycholate complex is sited close to amino acids Tyr126, Tyr239, Leu287, Leu272, and Lys137. For, Cu(II) deoxycholate complex, the residues of amino acids comprise of Pro132, Pro108, Gln110, Gly109, Ile200, Asn203, Val202, His246, Pro293 and Tyr154. The binding energy was determined from the docking reads for Co(II)–6LU7, Ni(II)–6LU7 and Cu(II)–6LU7 deoxycholate compounds were found to be −446.99, −500.52, −398.13 kcal mol⁻¹ individually.

Silver (Ag) particle is a promising photocatalyst material with relatively high catalytic activity and good absorption in the visible light region. A dendritic structure of Ag has been studied in the purpose to enhance photocatalytic activity due to a large surface area and active site number of the metallic Ag particles. In this work, the Ag dendritic structure was synthesized from a surfactant-free electrolyte using the square wave voltammetry technique. The time-dependent growth of the Ag dendrites and their photocatalytic activity on methylene blue (MB) photodegradation are reported. Morphological analysis exhibits the fractal dendritic structure of Ag was found to continuously grow by increasing the deposition time. The Ag dendrites showed a low charge transfer resistance (366.21 Ω) and high specific capacitance (2.09 F/g). A high rate of MB degradation (45.57%) under ultraviolet irradiation indicated that the Ag dendrites produced using this technique are effective for the photocatalytic degradation of MB dye.

The objective of this paper is to present the investigations of the heat transfer process carried out by means of the multi-ribbon mixer. It is shown that the heat transfer process for the synergic effect of the mixing process and the flowing liquid through the mixer has significantly higher values of the heat transfer coefficients than the mixer with motionless impellers. The empirical correlations between the heat transfer coefficient and the operational parameters obtained in this work can provide guidance for the design and operation of an apparatus equipped with the multi-ribbon impeller. These empirical correlations can be used to predict the heat transfer coefficient for the multi-ribbon mixer.

The presented work describes the autoxidation of alpha-pinene for the first time using a catalyst based on activated carbon from biomass with introduced Fe. The raw material for the preparation of the carbon material was waste orange peel, which was activated with a KOH solution. The following instrumental methods characterized the obtained catalyst (Fe/O_AC):N₂ adsorption at 77 K, XRD, UV, SEM, TEM, X-ray microanalysis, and catalytic studies. It was shown that the Fe/O_AC catalyst was very active in the autoxidation of alpha-pinene. The main reaction products were: alpha-pinene oxide, verbenone, verbenol, and campholenic aldehyde.

The carbonaceous precursor was obtained via pyrolysis of commercial aramid polymer (Kevlar). Additionally the precursor was activated at 1000°C in CO₂ atmosphere for different times. Obtained materials were characterised by BET; XPS; SEM and optical microscopy. The sorption capacities were determined by temperature swing adsorption performed in TGA apparatus for CO₂ and C₂H₄ gases. The obtained materials exhibit high difference in sorption of these gases i.e. 1.5 and 2.8 mmol/g @30°C respectively and high SSA ~1600 m²/g what can be applied in separation applications. The highest uptakes were 1.8 and 3.1 mmol/g @30°C respectively. It was found that the presence of oxygen and nitrogen functional groups enhances C₂H₄/CO₂ uptake ratio.

The main raw material of paper and cardboard used in packaging is cellulose. Cardboard packages made of cardboard, which can be produced in much different quality and weight, are obtained in numerous shapes and appearances^{1, 2}. Paper and cardboard packaging are among the most economical packaging types. Using less raw materials, more durable but thin, light, economical cardboard is produced^{2, 3}.

In this study, under equal printing conditions, test prints were made on cardboard substrates (for cardboard packaging) with mineral oil based, vegetable oil (soy oil) based and UV cured inks used for the printing of the same images. After these prints, the properties of mineral oil, vegetable oil and UV ink; the effect on the print results was measured from different ways (Chroma*, Print density, unprinted surface Gloss 75°, Print Gloss 60°). At the same time, the visual differences between the print results were determined by the optical imaging (SEM) method and were examined by the elemental analysis method.