Sharif Digital Repository

Gas-to-Liquid (GTL) is a multi-staged process in which natural gas is converted to liquid fuels. The stages of GTL process are discussed. A GTL plant with 10,000 bpd capacity and have similar specifications with the SASOL process was simulated using the Aspen-Plus software and the simulation results were compared with the SASOL process data. This is an abstract of a paper presented at the 18th International Congress of Chemical and Process Engineering (Prague, Czech Republic 8/24-28/2008)  

New dioxomolybdenum(VI) complex was prepared by reacting 1-(2,4-dihydroxybenzylidene)-N-methyl-N-phenylthiosemicarbazone (H2L) as ligand and [MoO2(acac)2] in acetonitrile solution. The doubly deprotonated ligand is coordinated to molybdenum through sulfur atom, hydrazinic nitrogen atom and phenolic oxygen atom. The resulting complex with the formula [MoO2L(CH3CN)] which contains an acetonitrile molecule in sixth site of coordination, was characterized by elemental analyses, 1H NMR, IR and electronic spectroscopic studies and single crystal X-ray diffraction analysis. This complex was tested as a catalyst for the homogeneous epoxidation of olefins using tert-butyl hydrogen peroxide (TBHP) as... 

A new cis-dioxo molybdenum(VI) complex was obtained by reaction of 2,4-dihydroxybenzylidene(5-N,N-methylphenylamino-1,3,4-thiadiazol-2-yl)hydrazone as ligand and [MoO2(acac)2] in methanol and was characterized by elemental analyses, 1H NMR, IR, and electronic spectroscopic studies. The complex was also analyzed by single-crystal X-ray diffraction. The structure determination revealed a distorted octahedral coordination geometry around molybdenum in which the tridentate NNO donor (L2-) is bonded to [MoO2]2+ through phenolic oxygen, hydrazinic nitrogen, and thiadiazole nitrogen. The sixth coordination site is occupied by a weakly bonded methanol. The complex was tested as a catalyst for... 

A new efficient catalytic system was investigated for the epoxidation of various olefins by cis-dioxo-bis[2-(2′-hydroxyphenyl)-oxazolinato]molybdenum(VI), cis-[MoO2(phox)2], and TBHP as oxidizing agent. Using this system as catalyst for the oxidation of aliphatic substrates at 80 °C gives the epoxide as the sole product with yields up to 100% and turnover frequency up to 5000 h-1. The efficiency of the catalyst is strongly influenced by the nature of solvent, reaction time and temperature, and a significant increase in the epoxide yields is observed in higher temperatures and longer reaction times. © 2009 Elsevier B.V  

The importance of the gas-to-liquid process is increasing due to growing demand for a high quality, less expensive, and cleaner fuel. Faujasite zeolites, e.g,. zeolites type X and Y, are well-known catalysts in the petrochemical industry. Faujasitic supports (mainly X zeolites) were prepared via hydrothermal synthesis with different Si/Al ratios from pure chemical materials and fly ash as a source of silicon. A high quantity of cobalt oxides was deposited on supports by varying samples Si/Al ratios during the zeolite preparation procedure. Using fly ash in synthesizing the zeolitic support resulted in a A-X zeolite material with a very high cation exchange capability and final cobalt... 

Several primary and secondary amines were added to α,β- unsaturated esters, nitriles, amides, and ketones to give the corresponding saturated amines mediated by solid lithium perchlorate under solvent-free and environmentally friendly conditions at room temperature. © 2003 Elsevier Ltd. All rights reserved  

An oxido-peroxido tungsten(VI) complex [WO(O2)L(CH 30H)] using salicylidene benzoyl hydrazine as a tridentate ONO donor Schiff base (H2L) has been synthesized and characterized by elemental analysis, IR, 1H NMR, molar conductance data, and single-crystal X-ray analysis. The complex was used as a catalyst for epoxidation of olefins and oxidation of sulfides. The results show that epoxides and sulfoxides were produced in high yield, turnover number, and selectivity  

A new manganese(III) complex [(N-O)2Mn(OAc)] was synthesized using 2-(2'-hydroxyphenyl)-5,6-dihydro-1,3-oxazine (N-O) as a bidentate O, N donor. The complex has been characterized by elemental analysis, IR, UV-vis spectroscopy, and X-ray structure analysis. Oxidation of sulfides and epoxidation of olefins, respectively, to their corresponding sulfoxides and epoxides were conducted by this catalyst using urea hydrogen peroxide as oxidant at room temperature under air. The catalyst is efficient in oxidation reactions giving high yields and selectivities  

A new oxido-peroxido molybdenum(VI) complex [MoO(O 2)L(CH 3OH)] was synthesized, using salicylidene benzoyl hydrazine as tridentate ONO donor Schiff base ligand (H 2L). The complex has been characterized by elemental analysis, IR, 1H NMR, molar conductance data, and finally by X-ray structure analysis. This complex functions as facile olefin epoxidation catalyst with hydrogen peroxide (H 2O 2) as terminal oxidant and sodium hydrogen carbonate (NaHCO 3) as a co-catalyst at room temperature. Catalytic potentiality of complex is also exhibited in oxidation of sulfides. The catalyst show very much efficient reactivity in the oxidation reactions giving high yield, turnover number (TON) and... 

The phenomenon of friction reduction was investigated by using a polymeric injection of a residual stream of turbulent flow known as the tomes phenomenon for a smooth flow without a roughness effect in 1975 by Virk. In the following years, by investigating the development of studies to reduce the friction in the turbulent stream by individuals such as torgeir, the effect of molecular weight, concentration and polymer thermodynamic conditions on friction reduction were investigated, and it was shown that by increasing the polystyrene concentration in the Toluene for turbulent flow, Reduced friction increases. Also, Fernandes and Mowal studied the effect of the polymer on friction reduction in... 

The synthesis of a Mo(VI) Schiff base complex, cis-[MoO2{(4,6-bis(tert-butyl)-2-{(benzyl)iminomethyl}phenolate)2}], cis-[MoO2(L)2] where L = 4,6-bis(tert-butyl)-2-{(benzyl)iminomethyl}phenol, derived from benzylamine and 3,5-di-tert-butylsalycilaldehyde is reported. Full characterization of this complex was accomplished with elemental analyses, spectroscopic studies (NMR, IR and electronic) and X-ray structure analysis. This complex was tested as a catalyst for the homogeneous oxidation of olefins. The Mo(VI) complex is catalytically active for the epoxidation of aliphatic substrates at 80 °C, yielding the epoxide as the sole product in yields up to 100% and turnover numbers up to 5000.... 

A simple, efficient, and general synthetic strategy has been developed for the synthesis of Michael adducts in the presence of solid lithium perchlorate under solvent-free conditions. Nucleophilic addition of thiols and indoles gave the corresponding Michael adducts in high yields. © 2005 Taylor & Francis  

The reaction of substituted dithiocarbamates with electrophilic alkenes in the presence of LiClO4 was investigated in an attempt to prepare numerous ethyl dithiocarbamates bearing β-electron-withdrawing-group substituents. The reaction conditions are mild, neutral, with extremely simple work-up procedures, and offer high yield. © 2005 Taylor & Francis Group Ltd  

A mixture of cobalt and manganese salts of p-aminobenzoic acid supported on silica gel catalyses the epoxidation of terminal olefins to the corresponding 1,2-epoxy compounds in the presence of oxygen  

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 novel binuclear Mn(II) complex based on a para-nitro substituted amidic ligand (N-(4-nitrophenyl)picolinamide) has been synthesized and characterized by X-ray crystallography. This complex shows a high degree of conversion and epoxide selectivity in Mukaiyama aerobic epoxidation reactions of cyclic olefins in mild conditions  

BACKGROUND: The clay treatment widely utilized to reduce unsaturated components in aromatic stream has a detrimental effect on catalyst lifetime. Due to the short lifetime of commercial clay, a huge number of studies have been carried out to address this problem over the last decade. This study aims to optimize the temperature for longer serviceability of clay by removal of unsaturated aliphatic components from aromatic streams through the adsorption and catalytic properties of clay. A novel process arrangement is introduced by scheduling the reuse of deactivated clay that is discarded after deactivation. RESULTS: Results showed that the suitable range of temperature for olefin removal 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 mathematical model for a fixed bed radial flow catalytic reactor was developed for dehydrogenation of heavy paraffins over Pt-Sn/Al2O3 catalyst. The model included appropriate kinetic rate expressions for the main dehydrogenation reaction as well as side reactions and catalyst deactivation. The reactor model consisted of a set of partial and ordinary as well as algebraic equations that were solved numerically to determine the concentration of various species along the radius of the bed as a function of time. The Nelder-Mead optimization method was used to obtain the optimum kinetic parameters. The validity of the model was demonstrated by comparing the predicted paraffin conversion and...