Sharif Digital Repository

Palladium catalysts supported on functionalized multi-wall carbon nanotubes were synthesized for hydro-purification of crude terephthalic acid containing 2100ppm 4-carboxybenzaldehyde (4-CBA) as impurity. PdCl2 and Pd(OAc)2 were used as precursors. Palladium loadings were 0.05 to 0.6wt.% with catalysts reduced at 200 to 400°C. Catalysts prepared from both precursors with least 0.3wt.% palladium resulted in 99%+ removal of 4-CBA. The most desired selectivity was obtained for the catalyst with PdCl2 as precursor, reduction temperature of 300°C, and palladium loading of 0.3wt.%. This catalyst had slightly better performance than the commercial catalyst (0.5wt.% of palladium on activated carbon)... 

Methanol conversion was investigated on dealuminated mordenite (DM) as well as a series of promoted DM (i.e., metal/DM) catalysts prepared by impregnation. Prepared catalysts characterized by the powder XRD, BET, and NH3-TPD techniques. Chemical analysis was performed using induced coupled plasma (ICP) method. The conversion of methanol over different metal/mordenite catalysts was compared at 460C and WHSV of 1 h-1. Several metals including Fe, La, and Ca had been used to prepare metal/DM catalysts, which displayed high selectivity toward propylene production. Ultimately, La/DM catalyst was determined to be the best material amongst those investigated for methanol conversion based upon its... 

A series of V2O5 catalysts supported on multiwall carbon nanotube (MWCNT), single wall carbon nanotube (SWCNT), and graphene were synthesized by hydrothermal and reflux methods for oxidative dehydrogenation of propane (ODHP) to propylene. The catalysts were characterized by techniques including the BET surface area measurements, XRD, FTIR, H2-TPR, NH3-TPD, FESEM, and UV-vis diffuse reflectance spectroscopy. The performance of the catalysts and the supports were subsequently examined in a fixed bed reactor. The main products were propylene, ethylene and CO x. The vanadium catalyst supported on graphene with C/V molar ratio of 1:1 synthesized through the hydrothermal method had the best... 

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  

Cobalt supported on carbon nanotubes (CNTs)-covered alumina has been recently developed and successfully utilized as a catalyst in Fischer-Tropsch synthesis (FTS). Problems associated with shaping of Co/CNTs into extrudates or pellets as well as catalyst attrition rendered these materials unfavorable for industrial applications. In this investigation regular γ- and nano-structured (N-S) alumina as well as CNTs-covered regular γ- and N-S-alumina supports were impregnated by cobalt nitrate solution to make new cobalt-based catalysts which were also promoted by Ru. The catalysts were characterized and tested in a micro reactor to evaluate their applicability in FTS. γ-Al2O3 was prepared by... 

Cobalt-based catalysts were prepared on gamma alumina supports, and their behaviour for different Fischer-Tropsch synthesis (FTS) conditions was assessed. Although Co/γ-Al 2O 3 is a well-known FTS catalyst, its durability ought to be improved to make the industrial process economically feasible. The effect of lanthanum doping on the catalyst lifetime was examined utilising reactor tests and catalyst characterization techniques including TPR, ICP and N 2 porosimetry. Reactor test results revealed that an optimum amount of lanthanum improved catalyst activity and selectivity. Increasing amounts of lanthanum doping up to about 1.1wt% seemed to modify the chemical composition of the support... 

A series of Cr-substituted Fe-Ti compounds were prepared by the co-precipitation method and were systematically investigated as catalysts for the selective catalytic reduction (SCR) of NO by NH 3. A variety of analytical techniques revealed that the Cr substitution amount affects the N 2 selectivity, SCR activity, redox behavior of NH 3/NO x, adsorption ability, and structure of catalysts in terms of surface properties, porosity, mobility of lattice oxygen, oxidative ability of Cr species, ratio of Bronsted acid sites and Lewis acid sites, NO x adsorption capacity, and structural disorder and distortion. In a series of Fe aCr 1-aTiO x (a = 1, 0.75, 0.5, 0.2, 0) catalysts, Fe 0.5Cr 0.5TiO x... 

In the current study, the hybrid effect of a corona discharge and γ-alumina supported Ni catalysts in CO 2 reforming of methane is investigated. The study includes both purely catalytic operation in the temperature range of 923-1023 K, and hybrid catalytic-plasma operation of DC corona discharge reactor at room temperature and ambient pressure. The effect of feed flow rate, discharge power and Ni/γ-Al 2O 3 catalysts are studied. When CH 4/CO 2 ratio in the feed is 1/2, the syngas of low H 2/CO ratio at about 0.56 is obtained, which is a potential feedstock for synthesis of liquid hydrocarbons. Although Ni catalyst is only active above 573 K, presence of Ni catalysts in the cold corona plasma... 

In this work, a fundamental kinetic model based upon the Hougen-Watson non-porosity formalism was derived and used to simulate dehydrogenation and oxidation axial flow reactors. In addition, partial pressure profiles of components during styrene production process inside porous catalyst were obtained using Dusty-Gas model. The preservation equations are adopted to calculate temperature and flow profiles in the reactors filled with iron-potassium promoted catalyst pellets. The presented mathematical model for ethylbenzene dehydrogenation consists of nonlinear simultaneous differential equations with multiple dependent variables. Simulation results such as selectivity and operating temperature... 

Dehydrogenation of ethylbenzene (EB) to produce styrene (ST) monomer is commercially performed over potassium-promoted iron oxide catalysts. Catalyst deactivation due to coke deposition and loss of potassium is a major operation and economic drawback in this process. To better evaluate the performance change of these catalysts over their life-cycle, dehydrogenation of EB to ST over the fresh and used commercial catalysts was experimentally investigated at temperatures from 590 to 639°C under atmospheric pressure. The fresh and the used catalysts were obtained from a styrene plant. The used catalyst had been continuously operated for two years under severe plant conditions. The catalyst... 

In this paper, the effects of two methods of iridium impregnation into HZSM-5 on catalyst stability, selectivity for propylene and byproducts in the conversion of methanol to propylene (MTP) were investigated in a continuous flow isotherm fixed-bed reactor. XRD, BET surface area, NH 3-TPD and ICP-AES analytical techniques were applied to define the physical and chemical characteristics of zeolites. The reaction was conducted at 480°C and 1 bar with WHSV = 1 h -1, and with an equal weight percent of methanol and water in the feed. The results revealed that iridium impregnation into HZSM-5 powder led to enhanced propylene selectivity (8%) and catalyst stability while iridium impregnation into... 

In this research, a palladium nanocatalyst was synthesised over a multi-walled carbon nanotube (MWCNT) support and then applied for selective hydrogenation of acetylene in an ethylene-richflow stream. This material displayed a very promising selectivity toward ethylene production with increasing temperature, and also suppressed oligomer formation during acetylene hydrogenation. New operating conditions for selective hydrogenation of acetylene in an ethylene-richflow were introduced. This nanocatalyst gave a considerably higher yield, as high as 93%, than that previously obtained for ethylene production. It was postulated that the governing mechanism for acetylene hydrogenation over 0.5 wt.%... 

Palladium nanocatalysts supported on reduced graphene oxide (rGO), multi walled carbon nanotubes (MWCNT), and rGO/CNT composite were synthesized by a wet impregnation method using PdCl2 as a precursor. Palladium loading was 0.3 wt %, and the catalysts were reduced at 300°C. The catalysts were characterized by inductively coupled plasma, Brunauer-Emmett-Teller (BET) analysis, Fourier transform infrared spectroscopy, X-ray powder diffraction, transmission electron microscopy, temperatue-programmed reduction, temperatue-programmed desorption, and Raman spectroscopy. The performance of the catalysts was investigated for hydro-purification of crude terephthalic acid (CTA) containing... 

A molybdenum complex, [MoO2Cl2(DMSO)2], was immobilized on amino propyl and Schiff base modified magnetic Fe3O4@SiO2 nanoparticles by covalent linkage. The resulting nanoparticles were used as efficient and recyclable catalysts for the selective oxidation of sulfides to sulfoxides using urea hydrogen peroxide as the oxidant. The complete characterization of catalysts was carried out by means of thermogravimetric analysis (TGA), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM), X-ray photoelectron spectroscopy (XPS), elemental analysis, FT-IR and Raman microprobe... 

Palladium catalysts supported on functionalized multi-wall carbon nanotubes were synthesized for hydro-purification of crude terephthalic acid containing 2100ppm 4-carboxybenzaldehyde (4-CBA) as impurity. PdCl2 and Pd(OAc)2 were used as precursors. Palladium loadings were 0.05 to 0.6wt.% with catalysts reduced at 200 to 400°C. Catalysts prepared from both precursors with least 0.3wt.% palladium resulted in 99%+ removal of 4-CBA. The most desired selectivity was obtained for the catalyst with PdCl2 as precursor, reduction temperature of 300°C, and palladium loading of 0.3wt.%. This catalyst had slightly better performance than the commercial catalyst (0.5wt.%... 

Two nanocatalysts of palladium over multi-walled carbon nanotubes (MWCNT) were synthesized and their catalytic properties evaluated in selective hydrogenation of acetylene. Different procedures were applied to synthesize catalysts which resulted in two distinct average particle sizes of palladium (Pd) over the MWCNT. The resulting catalysts displayed dissimilar NH3-TPD behaviors as well as different selectivity performances at lower temperatures. While enhancement of the hydrogen transfer mechanism occurred upon the temperature increase, similar behaviors for the aforementioned materials were obtained. Furthermore, it was revealed that the catalytic performance at higher temperatures did not... 

In this study, the influence of CO2 and CH4 on the performance and selectivity of Co-Ru/Al2O3 catalyst is investigated by injection of these gases (0-20 vol.% of feed) to the feed stream. The effect of temperature and feed flow rate are also inspected. The results show that low amounts of CO2 in the feed stream do not change the catalyst activity, but increasing the amount of CO2 (more than 10 vol.%), causes the CO conversion to decrease and the selectivity of heavy components to increase. Methane acts as an inert gas and does not affect the catalyst performance. Increasing feed flow rate has a negative effect on both CO conversion and heavy component selectivity. By raising the temperature,... 

The reaction of Fe(acac)3 and 2-(2′-hydroxyphenyl)oxazoline (Hphox) as a bidentate O,N donor ligand afforded a six-coordinated iron(III) complex [Fe(phox)2(acac)] with distorted octahedral configuration. The complex was isolated as an air-stable crystalline solid and characterized by elemental analysis, FTIR, solution electrical conductivity, and by single-crystal X-ray structure analysis. The structure, electronic properties, and vibrational normal modes of the complex were investigated by DFT. The use of this complex as a catalyst for the oxidation of sulfides to their corresponding sulfoxides using urea hydrogen peroxide as the primary oxidant was investigated. The catalyst shows very... 

The use of 1,3-bis(N-heterocyclic)carbene ligands with different alkyl wingtip groups (alkyl = methyl, isopropyl and tert-butyl) is an effective method for the palladium-catalysed direct S-arylation of methylphenyl sulfoxide and C-C coupling of various of aryl halides with alkenes. The reactions proceed in moderate to good yields. Interestingly, it is shown experimentally that, by using bulkier bidentate N-heterocyclic carbene ligands, more selective catalytic systems towards cis products in Heck coupling reactions can be achieved  

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...