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)... 

The 2,6-bis(diphenylphosphino)pyridine/palladium catalytic system successfully catalyzes the Heck coupling reaction of less reactive aryl chlorides as well as aryl bromides with styrene to give the corresponding olefins in reasonable yields. TBAB (tetrabutylammoniumbromide) as an additive was found to be essential for these reactions. The results of Heck reaction exhibited a high selectivity (>99/1) favoring the trans product  

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.%... 

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.%... 

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... 

Liquid phase hydro-purification of crude terephthalic acid (CTA) was performed using supported Pd and Pd-Sn catalysts on functionalized multi-wall carbon nanotubes (FMWCNT). Pd/FMWCNT catalysts were prepared by wet impregnation with Pd loadings of 0.05 to 0.6 wt.%. Pd-Sn/FMWCNT catalysts were prepared by co-impregnation (CI) and successive impregnation (SI) using 0.3 wt.% Pd loading and Sn/Pd molar ratios of 0.1 and 0.35 for the CI method and 0.05 to 0.35 for the SI method. Pd loading of 0.3 wt.% for Pd/FMWCNT was sufficient to decrease the 4-carboxybenzaldehyde (4-CBA) content of CTA from 2100 ppm to 5.5 ppm without excessive hydrogenation of terephthalic acid (TA). The commercial catalyst... 

Aryl halides and especially inactive aryl chlorides were coupled to benzenoid aromatic rings in a Suzuki–Miyaura coupling reaction in the absence of organic solvents and toxic phosphine ligands. The reaction was catalysed by a recoverable magnetic nanocatalyst, Pd@Fe3O4, in aqueous media. This method is green, and the catalyst is easily removed from the reaction media using an external magnetic field and can be re-used at least 10 times without any considerable loss in its activity. The catalyst was characterized using scanning and transmission electron microscopies, thermogravimetric analysis, inductively coupled plasma spectroscopy, Fourier transform infrared spectroscopy, CHN analysis,...