Current Issue : July-September Volume : 2025 Issue Number : 3 Articles : 5 Articles
With the widespread application of lead-free solder, solder represented by the SAC series has been widely used. However, with the miniaturization and multifunctionalization of electronic devices, the distance between solder joints is becoming increasingly smaller, and the problem of electrochemical migration caused by Ag in the SAC series is gradually emerging. Therefore, it becomes imperative to develop a solder that has a melting point, mechanical properties, and other properties similar to those of the SAC series but does not contain silver. In this study, 1–3% of Bi and 1–3% of In were added to the Sn-0.7Cu solder to investigate the effects of these elements on the melting characteristics, microstructure, mechanical properties, wettability, and electrical conductivity of the Sn-0.7Cu solder. Due to the addition of Bi and In elements, the melting point of the Sn-0.7Cu solder was lowered, the shear strength was improved, and the solderability was enhanced, but the electrical conductivity was reduced. This article obtained the mechanism of the influence of Bi and In elements on the properties of the Sn-0.7Cu solder through experiments and theoretical analysis, providing a certain degree of theoretical support for the development of silver-free solder....
The so far unattended version of the Hirao reaction involving the coupling of the less reactive chloroarenes with >P(O)H reagents, such as diarylphosphine oxides, diethyl phosphite, and ethyl phenyl-H-phosphinate, was investigated in detail using Pd(OAc)2 as the catalyst precursor, and applying some excess of the P-reagent to provide the ligand via its trivalent tautomeric (>P-OH) form. In the presence of triethylamine, no P–C coupling took place, meaning that there was a need for a stronger base, an alkali carbonate. The solvent had a significant effect on the efficiency of the Hirao reaction. The optimum conditions (10% of the Pd(OAc)2, 1.3 equiv. of the P-reagent, 1.1 equiv. of the alkali carbonate, 135–150 ◦C) explored herein were applied in the synthesis of diaryl-phenylphosphine oxides, aryl-diphenylphosphine oxides, diethyl arylphosphonates, and ethyl diphenylphosphinate. Theoretical calculations performed at the M06-2X/6-31G(d,p)[PCM(MeCN)] level also justified coupling with the chloroarenes under appropriate conditions, and were in accord with the experimental results revealing the unsuitability of triethylamine as a base and the need for an alkali carbonate. The new protocol elaborated herein is more practical and “greener” than the version with bromoarenes, and embraces a wide substrate scope....
The objective of this study was to examine the photodegradation of rimsulfuron in natural waters from the Niayes agricultural zone in Senegal. This was conducted in both the presence and absence of oxalic acid, which acts as a photosensitiser. The photodegradation values of rimsulfuron in distilled water and natural waters were found to be 15.52% and 6.3% to 7.19%, respectively. The results demonstrate that rimsulfuron is relatively stable in natural waters under solar radiation in the absence of photosensitiser. The photodegradation percentage in distilled water was 68.57%, while the range in natural water was from 16.98% to 40.32%. The results clearly show that oxalic acid significantly accelerates the photodegradation of the herbicide rimsulfuron. The photodegradation reaction half-life time varies considerably, from 144.41 to 693.15 minutes, with the highest value observed in surface water (runoff water), which generally contains a greater quantity of dissolved organic matter. We then examined the herbicidal activity of the compound in question. The results of this study indicate that the herbicidal activity of rimsulfuron may be attributed to either the initial product or a combination of the initial product and its photoproduct....
Environmental legislation has focused its attention on improving air quality. In this context, the presence of sulfur compounds in fuels, such as diesel and gasoline, is undesirable. When sulfur is combusted, compounds are emitted as SOx (SO2 and SO3) into the atmosphere, causing acid rain and respiratory diseases. For this reason, environmental norms have been established to reduce the sulfur content of fuels. Sulfur (mainly as alkylbenzothiophenes, dibenzothiophenes and alkyldibenzothiophenes) is removed in refineries through a process called hydrodesulfurization (HDS). HDS is performed at an industrial level with the use of NiMo, CoMo or NiW catalysts supported on alumina. Unsupported MoS2 (bulk) catalysts have recently attracted attention due to their high activity and selectivity in HDS. In this study, bulk NiMo catalyst precursors were synthesized using solvothermal methods with varying pH and solvothermal synthesis time. The precursors and catalysts were characterized using scanning electron microscopy with energy dispersive X-ray spectroscopy (EDS) microanalysis, X-ray diffraction (XRD), textural properties using liquid nitrogen physisorption at 77 K, Raman spectroscopy and high-resolution transmission electron microscopy (HTREM). The results indicate that the morphology of the NiMoO4 precursors synthesized in an ethanol/water mixture varies, forming “grains,” “flakes” or “rods,” depending on the dwell time and synthesis conditions. The catalytic activity results show that the bulk NiMo catalyst synthesized at 2 h presented higher selectivity and catalytic activity in the HDS of 4,6-DMDBT when compared to a supported reference catalyst (NiMo/γ-Al2O3)....
Ferromagnetic Fe3O4 nanoparticles were synthesized using water as the solvent through the sol-gel method, which was selected for its cost-effectiveness, simplicity, and eco-friendly nature. The synthesized nanoparticles were characterized using a variety of techniques, including Fourier Transform Infrared (FTIR) spectroscopy, X-ray powder diffraction (XRD), Scanning Electron Microscopy (SEM), Thermogravimetric Analysis (TGA), and Vibrating Sample Magnetometer (VSM). These characterizations confirmed the successful formation of Fe3O4 nanoparticles. The FTIR spectra identified characteristic peaks corresponding to the functional groups present, and XRD analysis, using Scherer’s equation, determined an average crystalline size of 1.2 nm for the Fe3O4 nanoparticles. TGA results demonstrated the thermal stability of the nanoparticles, SEM imaging revealed distinct honeycomb- like structures for the nanoparticles synthesized with water as the solvent, while the VSM analysis was used to determine the magnetic behavior of the nanoparticles....
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