Palladium nanoparticles as reusable catalyst for the synthesis of N-aryl sulfonamides under mild reaction conditions

An efficient palladium nanoparticles-catalyzed N-arylation of sulfonamides and sulfonyl azides is described. This procedure serves as an active protocol for intermolecular C–N bond formation using Pd(OAc)₂ in PEG-400 under air. Aryl bromides and triflates react at 35°C, while aryl chlorides require heating to 50°C and give the desired products only in low yields. This reaction proceeds smoothly in acceptable yields using low catalyst loading.     

Effect of preparation and operation conditions on the catalytic performance of cobalt-based catalysts for light olefins production

Cobalt-based catalysts were prepared by precipitation method. This research investigated the effects of different supports cobalt loading, promoters, loading of promoters and calcination conditions on the catalytic performance of cobalt catalysts for Fisher-Tropsch synthesis (FTS). It was found that the catalyst containing 40 wt.% Co/TiO₂ promoted with 6 wt.% Zn was an optimal catalyst for the conversion of synthesis gas to hydrocarbons especially light olefins. The activity and selectivity of optimal catalyst were studied in different operational conditions. The results showed that the best operational conditions were the H₂/CO = 2/1 molar feed ratio at 240 °C and GHSV = 1100 h⁻¹ under atmospheric pressure. Characterization of catalysts were carried out by using X-ray diffraction (XRD), thermal gravimetric analysis (TGA), hydrogen temperature program reduction (H₂-TPR), N₂ physisorption measurements such as Brunauer-Emmett-Teller (BET) and Barrett-Joyner-Halenda (BJH) methods.     

Effect of different modified nanoclays on the kinetics of preparation and properties of polymer-based nanocomposites

Polymer-clay nanocomposites have been prepared by free radical and RAFT polymerizations. To investigate the effects of nanoclay content and its modification system on the kinetics of polymerization, two different commercial grades of clay including Na-MMT and Cloisite 30B have been used and a method has been developed for further modification of Na-MMT with two commercial modifiers containing either a long organic chain or a vinyl group. Also, kinetics of free radical and RAFT polymerizations of both styrene and methyl methacrylate in the presence of these nanoclays was studied. Morphology of the nanocomposites has been studied by XRD and the results have been assessed with TEM observations. Exfoliated structure was obtained for the nanocomposites with 1?wt.% of vinyl-containing clays. Thermogravimetric behavior of the nanocomposites has been studied by TGA. Incorporation of clays has resulted in an evident increase in thermal stability of both polymers.     

The control of abnormal grain growth in low-voltage SnO2 varistors by microseed addition

In this research, the addition effects of three different quantities of micron-sized seeds (microseeds) to a SnO₂ varistor prepared from nanomaterials on the microstructure and electrical properties were studied. Moreover, surge-withstanding capability of low-voltage SnO₂ varistors was investigated. The X-ray diffraction pattern disclosed a single phase SnO₂ for microseed grains. The morphological features of samples were characterized using scanning electron microscopy. The abnormal distribution of grain size with elongated grains of SnO₂ in fine grains matrix was observed in sintered samples without microseeds. The low content of microseed addition (0.3 wt%) had not controlled abnormal grain growth, however, it increased mean grain size to 37 µm. Although the high content of microseeds (7.5 wt%) stopped abnormal grain growth, it had a negative effect on relative density and mean grain size. The normal grain size distribution with maximum mean grain size (45 µm) was obtained in samples containing 1.5 wt% microseeds. These samples showed the lowest breakdown field (240 V/cm) and the highest surge-withstanding capability (1.5 kA/cm²). Furthermore, the standard deviation of the electrical parameters of these samples was improved due to normal grain-size distribution.     

Experimental Study and Mathematical Modeling of NO Removal Using the UV/H2O2 Advanced Oxidation Process

An experimental study on NO removal via UV/H₂O₂ process was conducted in a semi‐continuous bubble‐column reactor and the effect of some operation parameters including NO initial concentration and gas flow rates on removal efficiency was investigated. Applying UV light increased the efficiency significantly. The steady‐state removal efficiency was found to be higher at the lower gas flow rates. The bubble size as an important factor in mass transfer calculations and modeling procedure was determined at different gas flow rates using bubble photographs and image processing technique. In the ranges of flow rates studied here, the gas flow rate had no significant effect on the bubble diameter. A mathematical model was developed to describe the NO removal process. The model predictions were compared with existing experimental data, confirming a good agreement of the data.     

An ab initio study on properties of cationic chalcogen bonds in XF2Y+⋯NCZ (X═H,CN, F; Y═S,Se; Z═H,Cl, Br) complexes

The geometries, interaction energies, and bonding properties of cationic chalcogen bonds are studied in binary complexes XF₂Y⁺?NCZ (X═H, CN, F; Y═S, Se; Z═H, Cl, Br). The nature of these interactions is studied by a vast number of methods, including molecular electrostatic potential (MEP), Noncovalent Interaction Index (NCI), quantum theory of atoms in molecules (QTAIM), and natural bond orbital (NBO) analyses. The interaction energies of these complexes vary between ?20.94?kcal/mol in HF₂S⁺?NCH and ?33.72?kcal/mol in F₃Se⁺?NCBr. According to the QTAIM analysis, all these cationic chalcogen bonds are classified as a closed-shell interaction with a partial covalent character. Moreover, cooperative effects between cationic chalcogen bond and hydrogen or halogen bond interactions are studied in ternary XF₂Y⁺?NCZ?NH₃ complexes. These cooperative effects are analyzed in terms of the parameters derived from the QTAIM and NBO analyses, and electron density difference plots.     

Novel conductive magnetic nanocomposite based on poly (indole-co-thiophene) as a hemoglobin diagnostic biosensor: Synthesis,characterization and physical properties

The novel conductive nanocomposite has been successfully prepared by emulsion polymerization. First, magnetite nanoparticles were synthesized via coprecipitation reaction. Then, poly (indole-co-thiophene)@Fe₃O₄ nanocomposite was prepared via emulsion copolymerization of indole and thiophene monomers using sodium dodecyl sulfate as an emulsifier and ammonium persulfate as an oxidant in the presence of Fe₃O₄ nanoparticles. Characterization of the synthesized copolymer, Poly (In-co-T), and its magnetic nanocomposite were studied by Fourier transform infrared spectra, X-ray diffraction, scanning electron microscopy, thermal gravimetric analysis, differential scanning calorimetric, UV-vis spectrophotometer, and vibrating sample magnetometer. Also, the electrical conductivity of copolymer and nanocomposite were determined by four-probe instrument. Results showed a synergic effect in thermal stability by good interaction between polymer chain and magnetic nanoparticles. The conductivity of the nanocomposite was higher than bare copolymer, and increase of nanoparticles content caused an increment in the conductivity of the nanocomposites. The applicable properties of proposed conductive nanocomposite as a base at electrochemical biosensing have been investigated.     

Au/PANA/PVAc and Au/P(ANA-co-CNTA)/PVAc electrospun nanofibers as tyrosinase immobilization supports

Au/poly anthranilic acid/poly vinyl acetate and Au/poly(anthranilic acid-co-3-carboxy-N-(2-thenylidene)aniline)/poly vinyl acetate nanofibers through electrospinning and their modification with covalent tyrosinase (Ty) immobilization was performed. It was realized by surface activation using N-(3-dimetylaminopropyl)-N-ethylcarbodimide hydrochloride/N-hydroxysuccinimide chemistry. Electrochemical impedance spectroscopy (EIS), FTIR–ATR, Raman spectroscopy, and bicinchoninic acid assay analyses demonstrated that Ty was stably and covalently bonded onto the nanofibers. Increase in surface roughness [atomic force microscopy (AFM)] and the presence of Cu atoms in the nanofiber composition after enzyme immobilization confirmed the Ty immobilization. The charge transfer resistances of the nanofibers decreased due to changes in the nanofiber surfaces after attachment of enzyme.