Sharif Digital Repository

In this study by Thermal Chemical Vapor Deposition (TCVD) method, the synthesis of carbon nanotubes (CNTs) and temperature affects on the grown CNTs on the NiSio2 catalyst and 304-type stainless steel was investigated. The purification of the grown CNTs on the 304-type stainless steel was also investigated in this study. The synthesis and purification of the samples were characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), termogravimetric analysis (TGA) and Raman spectroscopy. Our obtained result by SEM and TEM shows that densities of CNTs growth on the 304-type stainless steel are more than the CNTs growth on the NiSio2 catalyst and both of them have... 

This study was designed to compare one-step, two-step and spent medium bioleaching of spent catalyst by adapted Penecillum simplicissimum in batch cultures. Penecillum simplicissimum which was adapted to heavy metal ions Ni, Mo, Fe, and W grew in the presence of up to 5 %w/v of spent catalyst in the medium. The main lixiviant in bioleaching was gluconic acid which was produced mainly in present and absence of spent catalyst. A total of 3 %w/v spent catalyst generally gave maximum extraction yields in two-step bioleaching process, which the amounts of leached metals were 100 % of W, 100 % of Fe, 92.7 % of Mo, 66.43 % of Ni, and 25 % of Al. The red pigment produced by fungus could also... 

A heterogeneous magnetic copper catalyst was prepared via anchoring of copper sulfate onto multi-layered poly(2-dimethylaminoethyl acrylamide)-coated magnetic nanoparticles and was characterized using various techniques. The catalyst was found to be active, effective and selective for one-pot three-component reaction of alkyl halide, sodium azide and alkyne, known as copper-catalyzed click synthesis of 1,2,3-triazoles. As little as 0.3 mol% of catalyst was found to be effective under the optimum conditions. The catalyst could also be recycled and reused up to seven times without significant loss of activity. Thermal stability, high loading level of copper on catalyst, broad diversity of... 

Abstract: Polyoxometalate-functionalized magnetic nanoparticles (Fe3O4@SiO2–MnPOW) were successfully synthesized via covalent anchoring of Mn(II)-substituted phosphotungstate on ammonium-modified Fe3O4@SiO2 nanoparticles. The complete characterization of nanoparticles has been carried out by scanning electron microscope, energy-dispersive X-ray, X-ray diffraction, Fourier transform infrared and elemental analysis. The resulting nanocomposites were efficient catalysts for the selective oxidation of sulfides with different green oxidants in good to excellent yields and also high selectivity. Leaching and recycling tests showed that the nanocatalyst can be reused several times without... 

Palladium nanoparticles immobilized on a cross-linked imidazolium-containing polymer were evaluated as a catalyst for Suzuki carbon-carbon cross-coupling reactions using water as the solvent. The nanocatalysts show good catalytic activities for aryl iodides and aryl bromides and moderate activity with aryl chloride substrates. Coupling of sterically hindered substrates could also be achieved in reasonable yields. The heterogeneous catalyst is stable, can be stored without precautions to exclude air or moisture, and can be easily recycled and reused  

Molybdenum(VI)–oxodiperoxo complex containing an oxazine ligand, ([MoO(O2)2(phox)], phox: 2-(2′-hydroxyphenyl)-5,6-dihydro-1,3-oxazine) was conveniently synthesized and immobilized onto chloro-functionalized mesoporous silica SBA-15 by covalent bonding between the chloropropyl group on the internal surface of the pores and the nitrogen atom of oxazine ligand yielding [MoO(O2)2(phox)]/SBA-15. The resulting material was characterized by FT-IR, TGA, XRD, SEM, TEM, EDX, ICP-AES, BET and UV–vis spectroscopy. The heterogeneous catalyst [MoO(O2)2(phox)]/SBA-15 was employed in the epoxidation of alkenes, exhibiting high catalytic performance and selectivity for epoxide similar to that of homogeneous... 

A new magnetic heterogeneous catalyst was synthesized by immobilization of nickel ions onto a cross-linked polymeric nanocomposite composed of cyanuric chloride, ethylenediamine and functionalized magnetic nanoparticles. The resulting nitrogen rich support was capable of adsorbing large amounts of nickel ions (1.20 mmol g−1). The synthesized catalyst was characterized using AAS, TEM, FT-IR, EDX, TGA, SEM, BET and XRD techniques. The performance of the prepared catalyst was investigated in the C-N coupling of arylamines with aryl boronic acids. The reaction was carried out under a mild condition and good to moderate to good yields of products was obtained using only 5.0 mol% of the catalyst.... 

Kinetic and morphological aspects of slurry propylene polymerization using a MgCl2-supported Ziegler-Natta catalyst synthesized from a Mg(OEt)2 precursor in the presence and absence of two different external donors are investigated. The kinetic profiles show similar trend in presence and absence of donors. The Mg(OEt)2-based catalyst show a mild activation and a long-standing activity with good replication of the catalyst particles. The results show that synthesized Mg(OEt)2-based Ziegler-Natta catalyst presents a highly stable polymerization activity and good replication due to the uniform Ti distribution all over the catalyst particles. © 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim  

An efficient synthesis of tetrahydrobenzofurans is carried out in one pot through the reaction of 1,3-diketone and phenacyl bromides compound using a heterogeneous basic nano particles copper oxide catalyst. The protocol offers advantages in terms of higher yields, short reaction times, and mild reaction conditions, with reusability of the catalyst. © 2009 Elsevier B.V. All rights reserved  

A two-stage thermocatalytic upgrading process using a novel catalyst was investigated to produce light olefins and liquid fuels from fuel oil. The upgraded oil from the first thermal stage demonstrated lower viscosity and higher crackability compared to the virgin feedstock. In the next step, the vapor-phase catalytic cracking of the upgraded fraction was implemented over a novel nanoporous composite catalyst, characterized by the XRD, FTIR, NH3- TPD, and N2 physisorption techniques. In total, more than 55 wt% of light olefins, particularly propylene (25.5 wt%) together with 25.4 wt% and 32.5 wt% of gasoline and diesel fuel were obtained in this process. © 2019, © 2019 Taylor & Francis... 

An improved and efficient method for the synthesis of 1- & 5-substituted 1Htetrazole derivatives was described in the presence of nano-ordered MCM-41-SO3H as an effective heterogeneous catalyst. This metal-free protocol, [2 + 3] cycloaddition of sodium azide to various nitriles or ethyl N-phenyl formimidate intermediate under mild reaction conditions, provides a wide range of 1H-tetrazoles in good to excellent yields. The catalyst was reused five times without significant loss of catalytic activity. © 2019 Sharif University of Technology. All rights reserved  

An improved and efficient method for the synthesis of 1- & 5-substituted 1Htetrazole derivatives was described in the presence of nano-ordered MCM-41-SO3H as an effective heterogeneous catalyst. This metal-free protocol, [2 + 3] cycloaddition of sodium azide to various nitriles or ethyl N-phenyl formimidate intermediate under mild reaction conditions, provides a wide range of 1H-tetrazoles in good to excellent yields. The catalyst was reused five times without significant loss of catalytic activity. © 2019 Sharif University of Technology. All rights reserved  

In this research, a series of NiO–MgO–SiO2 catalyst samples with various nickel contents (5, 10, 15 and 20 wt %) were prepared by a co-precipitation method followed by a hydrothermal treatment and employed in propane steam reforming. The analyses revealed that the enhancement of the nickel content up to 15 wt % improved the propane conversion to 98.6% at 550 °C. Nonetheless, further increase in the nickel loading reduced the catalyst activity due to the formation of larger and more poorly dispersed active sites. Besides, 15 wt % nickel loading led to the high resistance against coke deposition with no detectable carbon on the catalyst surface. In addition, it was revealed that, the decrease... 

The solubility of Pd(NO3)2 in water is moderate whereas it is completely soluble in diluted HNO3 solution. Pd/MIL-101(Cr) and Pd/MIL-101-NH2(Cr) were synthesized by aqueous solution of Pd(NO3)2 and Pd(NO3)2 solution in dilute HNO3 and used for CO oxidation reaction. The catalysts synthesized with Pd(NO3)2 solution in dilute HNO3 showed lower activity. The aqueous solution of Pd(NO3)2 was used for synthesis of mono-metal Ni, Pd and bimetallic PdNi nanoparticles with various molar ratios supported on MOF. Pd70Ni30/MIL-101(Cr) catalyst showed higher activity than monometallic counterparts and Pd + Ni physical mixture due to the strong synergistic effect of PdNi nanoparticles, high distribution... 

The solubility of Pd(NO3)2 in water is moderate whereas it is completely soluble in diluted HNO3 solution. Pd/MIL-101(Cr) and Pd/MIL-101-NH2(Cr) were synthesized by aqueous solution of Pd(NO3)2 and Pd(NO3)2 solution in dilute HNO3 and used for CO oxidation reaction. The catalysts synthesized with Pd(NO3)2 solution in dilute HNO3 showed lower activity. The aqueous solution of Pd(NO3)2 was used for synthesis of mono-metal Ni, Pd and bimetallic PdNi nanoparticles with various molar ratios supported on MOF. Pd70Ni30/MIL-101(Cr) catalyst showed higher activity than monometallic counterparts and Pd + Ni physical mixture due to the strong synergistic effect of PdNi nanoparticles, high distribution... 

In this contribution, NiO-MgO-SiO2 catalyst was prepared and calcined at different temperatures of 500, 600, 700 and 800 °C. The resulting samples were characterized by BET-BJH, XRD, TPX, CO-chemisorption, EDS and SEM analyses. These were employed toward syngas production via propane dry reforming. The increment in the calcination temperature from 500 to 800 °C decreased the basicity of the catalysts. In addition, the active surface area and Ni dispersion were gradually declined by increasing the calcination temperature from 600 to 700 °C due to active metal sintering during the activation process. The calcined sample at 600 °C displayed the highest propane and CO2 conversions of 93% and 78%... 

The great promise of electrochemical water splitting for green and sustainable hydrogen fuel production has motivated researchers to strive for more efficient and low-cost catalysts based on non-precious metals. In this study, MoS2 nanoflowers decorated with CuCo2O4 were successfully synthesized, and their catalytic activities toward the electrochemical hydrogen evolution reaction (HER) in an alkaline medium were investigated. The composition, structure, and morphology of the as-synthesized catalysts were explored by various techniques such as FT-IR, XRD, BET, SEM, and TEM. To maximize the catalytic activity, the composition of the nanocomposites was systematically varied. Catalytic results... 

The present study aims to convert waste cooking oil (WCO) into biodiesel via phosphomolybdic acid (H3PMo12O40, PMA) supported on Clinoptilolite as a novel green acid catalyst through an electrolysis procedure. The prepared catalysts were characterized by XRD, FTIR, FESEM, EDS, Elemental map, and TEM analyses. The effect of four independent variables on biodiesel yield including methanol to oil molar ratio (6:1–14:1), catalyst weight (2–5 wt%), time (3–5 h), and voltage (15–35 V) was optimized and evaluated by the response surface methodology (RSM) employing central composite design (CCD). The maximum value of biodiesel yield was 96% under the optimal conditions, including the methanol to oil... 

In the present study, the ACF-TiO2 catalyst was synthesised and used as a catalyst for the destruction of toxic cyanide in both synthetic and real industrial wastewaters. The ACF-TiO2 catalyst was found to be micro-porous with the BET surface area of 163 m2/g. The effect of different operational parameters such as catalyst concentration, cyanide concentration, operation time, and ozone concentration were target parameters in the present study. The findings show that 500 mg/L of catalyst is the optimum value for the photocatalytical process to completely oxidise 25 mg/L of cyanide within 10 min. While it was found that 300 mg/L of catalyst in the presence of 200 mg/h ozone is enough to remove...