Sharif Digital Repository

Due to the high activity of Au nanoparticles (NPs) for various reactions, many researchers have tried to develop heterogeneous catalysts in order to prevent irreversible agglomeration of Au NPs. Herein, magnetic graphene oxide modified with polyaniline (PANI) was used as a support for Au NPs that brings together advantages including: uniform dispersal of the catalyst in water,alarge surface area related to the graphene oxide; easy electron transfer in chemical reactions and good attachment of Au NPs to the support associated with PANI; and finally facile recovery in the presence of a magnetic field. Catalytic reduction of different analytes (Congo red, methylene blue, rhodamine B and 4-nitro... 

In this study, a series of Ni nano-catalysts supported on Al2O3 and MgO were prepared through the co-precipitation technique. Effects of the Al/Mg ratio on physicochemical characteristics of Ni/Al2O3–MgO catalysts were examined. Moreover, catalytic performance was investigated in order to determine the optimum catalyst for H2 production in aqueous phase reforming (APR) of glycerol. It was revealed that, the APR activity of synthesized catalysts strongly depended on the aforementioned ratio. In addition, it was observed that, the catalytic activity of Ni/MgO and Ni/Al2O3 samples were both lower than that of the corresponding mixed oxide supports. Furthermore, it was shown that, amongst the... 

Background: Kinetic andmorphological aspects of slurry propylene polymerization using a MgCl2-supported Ziegler-Natta catalyst synthesized from a Mg(OEt)2 precursor are investigated in comparison with a ball-milled Ziegler-Natta catalyst. Results: The two types of catalyst show completely different polymerization profiles: mild activation and long-standing activity with good replication of the catalyst particles for the Mg(OEt)2-based catalyst, and rapid activation and deactivation with severe fragmentation of the catalyst particles for the ball-milled catalyst. The observed differences are discussed in relation to spatial distribution of TiCl4 on the outermost part and inside of the... 

A mild and practically-convenient one-pot procedure for the direct Mannich reaction has been developed using a condensation of amines, aldehydes and unmodified ketones under solvent free conditions in the presence of Znl 2 with good to excellent yields. The present methodology offers several advantages, such as excellent yields, simple procedures, short reaction times and milder conditions with very small amounts of catalyst. Furthermore, it is the first time that the catalytic activity of several catalysts under solvent free conditions has been studied. It was found that both the diastereoselectivity and the rate of reaction were improved with various Lewis acids and metal oxides. However,... 

A comprehensive study was carried out for the first time on the acidity of eleven different leaves. After functionalization of the leaves with –SO3H groups, the most acidic one was magnetized using nickel ferrite nanoparticles. This novel, inexpensive, green and biodegradable catalyst showed high activity in the synthesis of pyrazoline and 2-amino nicotinonitriles. Some compounds are new and have never been synthesized before and confirmed by FT-IR, 1H NMR and 13C NMR analysis. All of these compounds possess multiple biological activities. The heterogeneous magnetic catalyst (NiFe2O4-Alnus-SO3H) was characterized by various physicochemical techniques such as FT-IR spectroscopy, field... 

Methane steam reforming (MSR) is an assuring reaction using steam to produce H2 as clean energy over a nicκel-based catalyst. We synthesized mesoporous monometallic NiMgAl2O4 and bimetallic NiCoMgAl2O4 catalysts in a two-step combustion method using a mix of fuels and powder metallurgy. BET-BJH, XRD, TGA, TPR, FESEM, and EDX-mapping characterized surface area, porosity, morphology, crystalline structure, and metal-support interaction behavior. The products exhibited strong interaction of well-structured MgAl2O4 spinel with NiO, in both specimens. The MSR evaluation tests at 750 °C under atmospheric pressure, CH4:H2O feed ratio of 1:1.2 showed the bimetallic catalyst has the highest... 

In this article, the transesterification of waste cooking oil (WCO) to biodiesel fuel (BDF) has been studied using KOH loaded on millimetric γ-Al2O3 particles in a novel type of two-impinging-jets reactor (TIJR). The effects of various parameters such as KOH loading (wt %), catalyst loading, and methanol-to-oil molar ratio on the BDF yield were studied. The catalyst particles with a KOH loading of 25 wt % at appropriate reaction conditions (i.e., catalyst loading = 4 wt % and methanol-to-oil molar ratio = 15:1) and at 65 °C were used in the TIJR. The influences of various operating and design parameters such as jet Reynolds number value, feed flow rate, jet diameter, and the internozzle... 

An efficient method is reported for selective oxidation of various types of sulfides to sulfoxides and sulfones in good to high yields using 30% H 2O2 in the presence of catalytic amounts of molybdate-based catalyst in acetonitrile as solvent at room temperature. The catalyst can be easily recovered and reused for seven reaction cycles without considerable loss of activity  

Silica gel-confined ionic liquid (IL) is a class of heterogeneous catalysts with broad catalytic applications. Leaching of the IL from the surface of the support is the major drawback of these catalysts, which reduce the catalyst efficiency during the chemical reactions. To investigate the effect of the hydrogen bonding on the leaching phenomena, the interaction between the 1-ethyl-3-methylimidazolium-based IL with various anions (Cl-, Br-, HSO4 -, NO3 -, BF 4 -, and PF6 -) and the surface of the silica gel were studied using density functional theory. Hence, a hydroxylated cage-like cluster of silica gel, Si4O6(OH), was selected to mimic the surface. The values of ÎEinteraction show that... 

An acid treatment of the cordierite monolith followed by coating of the CNT onto it by means of catalytic decomposition of methane was performed. The resulting material utilized as the support for the CoMo catalyst. The characterization outcomes showed that the CNTs were distributed uniformly on the surface of the monolith leading to a high BET surface area and relatively good adhered mesoporous layer of CNTs. Moreover, the catalytic activity of the resulting catalysts determined in an HDS reaction of naphtha. It was concluded that the activity of the CoMo catalyst over the CNT coated monolithic support (FACNT) was higher than that of the CoMo deposited onto the acid-treated monolith and... 

A novel silica-functionalized ammonium tungstate interphase catalyst has been reported as a non-nitric acid route for adipic acid production from one-pot oxidative cleavage of 30% hydrogen peroxide and catalytic amounts of p-toluenesulfonic acid (PTSA). The catalyst has been simply prepared by commercially available starting material. The structure of the catalyst has been investigated using FT-IR spectroscopy, atomic absorption, TEM, SEM and XRD analysis. The catalyst has shown good to high activity even up to 10 runs of reaction. Simple preparation of the catalyst, avoids using harmful phase transfer catalyst (PTC) and/or chlorinated additives are among the other benefits of this work  

Propane dehydrogenation was carried over a commercial Pt-Sn/γ-Al 2O3 catalyst at atmospheric pressure and reaction temperatures of 580, 600, and 620°C and WHSV of 11 h-1 in an experimental tubular quartz reactor. Propane conversions were measured for catalyst time on stream of up to nine days. The amounts of coke deposited on the catalyst were measured after one, three, six, and nine days on stream using a thermogravimetric differential thermal analyzer (TG-DTA) for each reaction temperature. The coke formation kinetics was successfully described by a coke formation model based on a monolayer-multilayer mechanism. In addition, catalyst deactivation was presented by a time-dependant... 

Supported iron oxide nanoparticles are found to be efficient and recoverable catalyst in the selective oxidation of thiols to their corresponding disulfides using hydrogen peroxide as green oxidant at room temperature. The protocol features an easy work-up, simplicity and the utilizing mild reaction conditions, as well as high selectivity toward disulfides, are highly advantageous compared to alternative reported methodologies. The supported iron oxide nanoparticles could be easily recovered and reused several times without any loss of activity. ICP-MS results prove that there is no metal leaching observed, and demonstrating the stability of the catalyst under the reaction conditions  

We have evaluated the catalytic activity of a molybdenum(VI) oxo-peroxo complex through the oxidation and reduction of sulfur-based compounds. Arylalkyl, diaryl and dialkyl sulfides are selectively oxidized to corresponding sulfoxides, with tert-butyl hydroperoxide (TBHP), in the presence of MoO(O 2)(phox) 2 complex as catalyst. This molybdenum complex was also found to be an efficient catalyst for the deoxygenation of sulfoxides to sulfides with PPh 3 in excellent yields and chemoselectivity  

This study was designed to compare one-step, two-step and spent medium bioleaching of spent catalyst by adapted Aspergillus niger in batch cultures. Aspergillus niger, which was adapted to heavy metal ions, Ni, Mo, Fe, and W, was grown in medium containing up to 5% (w/v) of spent catalyst. The main lixiviant in bioleaching was gluconic acid, which was produced at all pulp densities in the one-step bioleaching process. Gluconic acid was also produced in the two-step bioleaching process when the spent catalyst was present at pulp densities greater than 1% (w/v). In the spent medium leaching, however, the primary agent was citric acid. The pulp density of the spent catalyst was varied, and this... 

Silver (0) nanoparticles supported on silica-coated ferrite were synthesized to be used as an efficient and recyclable heterogeneous catalyst for oxidant-free dehydrogenation of alcohols to the corresponding carbonyl compounds. The catalyst can be easily recovered and reused for 8 reaction cycles without considerable loss of activity. The facile recovery of the catalyst is carried out by applying an external magnetic device. The catalyst was fully characterized by the techniques of TEM, SEM, XRD, EDS, ICP-AES, and VSM. This journal is  

A metal-organic framework [Co3(BDC)3(DMF)2(H2O)2] was synthesized and structurally characterized. X-ray single crystal analysis revealed that the framework contains a 2D polymeric chain through coordination of 1,4-benzenedicarboxylic acid linker ligand to cobalt centers. The polymer crystallize in monoclinic P21/n space group with a=13.989(3) Å, b=9.6728(17) Å, c=16.707(3) Å, and Z=2. The polymer features a framework based on the perfect octahedral Co-O6 secondary building units. The catalytic activities of [Co3(BDC)3(DMF)2(H2O)2]n for olefins oxidation was conducted. The heterogeneous catalyst could be facilely separated from the reaction mixture, and reused three times without significant... 

A novel magnetic heterogeneous copper catalyst was synthesized by immobilization of copper ions onto triazole functionalized Fe3O4. The catalyst was fully characterized by FT-IR, TGA, CHN, SEM, TEM, EDX and atomic adsorption spectroscopy. The resulting catalyst was used in the synthesis of 1,2,3-triazoles via a one-pot three component reaction of alkynes, alkyl halides, sodium azides under green conditions. The catalyst was reused ten times and no significant loss of activity was observed  

In this study nickel ferrite magnetic nanoparticles were applied as an efficient and reusable catalyst in the four-component synthesis of substituted pyrroles under neat conditions. The reaction was conducted using various amounts of catalyst at different temperatures and finally, application of 5 mol% of catalyst at 100 °C was determined as the optimum reaction condition. Results showed that nickel ferrite nanoparticles could catalyze the reaction at relatively short times (3-4 h) with high to excellent yields (70-96%). The catalyst could be recovered easily using an external magnetic field and reused nine times without any significant activity lost