Isomerization metal-zeolite catalyzed

Metal-Zeolite Catalyzed Light Paraffin Isomerization... 

The presence of metal may catalyze demethylation and can occur to some extent in catalysts where the metal function is under-passivated, as by incomplete sulfiding. This would convert valuable xylenes to toluene. The demethylation reaction is usually a small contributor to xylene loss. Metal also catalyzes aromatics saturation reactions. While this is a major and necessary function to facilitate EB isomerization, any aromatics saturation is undesirable for the process in which xylene isomerization and EB dealkylation are combined. Naphthenes can also be ring-opened and cracked, leading to light gas by-products. The zeolitic portion of the catalyst participates in the naphthene cracking reactions. Cracked by-products can be more prevalent over smaller pore zeolite catalysts. 

Isomerization of olefins or paraffins is an acid-catalyzed reaction that can be carried out with any number of strong acids, including mineral acids, sulfated metal oxides, zeolites and precious metal-modified catalysts [10]. Often the catalyst contains both an acid function and a metal function. The two most prevalent catalysts are Pt/chlorided AI2O3 and Pt-loaded zeolites. The power of zeoHtes in this reaction type is due to their shape selectivity [11] and decreased sensitivity to water or other oxygenates versus AICI3. It is possible to control the selectivity of the reaction to the desired product by using a zeoHte with the proper characteristics [12]. These reactions are covered in more detail in Chapter 14. 

Different catalysts bring about different types of isomerization of hydrocarbons. Acids are the best known and most important catalysts bringing about isomerization through a carbocationic process. Brpnsted and Lewis acids, acidic solids, and superacids are used in different applications. Base-catalyzed isomerizations of hydrocarbons are less frequent, with mainly alkenes undergoing such transformations. Acetylenes and allenes are also interconverted in base-catalyzed reactions. Metals with dehydrogenating-hydrogenating activity usually supported on oxides are also used to bring about isomerizations. Zeolites with shape-selective characteristics... 

When the hydrogenation function is embedded in the crystal voids of an MFI topology, the formation of trans-isomers is strongly reduced. After partial reduction of soy bean oil with such catalyst from an iodine value of 140 to 80, virtually no trans-isomers are obtained (56). This is the result of pore mouth catalysis combined with zeolite shape selectivity. Due to the bent character of the cts-isomer chains in triglycerides, trans-configured chains preferentially enter the pore mouths for hydrogenation. In this environment, metal-catalyzed cis-trans isomerization is restricted for steric reasons as multiple readsorption is minimal. 

On the other hand, it was proposed that acid catalyzed reactions such as skeletal isomerization of paraffin [2], hydrocracking of hydrocarbons [3] or methanol conversion to hydrocarbon [4] over metal supported acid catalysts were promoted by spillover hydrogen (proton) on the acid catalysts. Hydrogen spillover phenomenon from noble metal to other component at room temperature has been reported in many cases [5]. Recently Masai et al. [6] and Steinberg et al. [7] showed that the physical mixtures of protonated zeolite and R/AI2O3 showed high hydrocracking activities of paraffins and skeletal isomerization to some extent. 

Methylpentanes prevailed among the isomers produced by this pathway. Even a slight increase of support acidity enhanced isomerization over Pt-zeolites, by rendering both metal and acid catalyzed pathways operative [13-15],... 

The conversion of n-hexane over various Pt-zeolite catalysts responded strongly to changes in hydrogen pressures [13-15]. Increasing the hydrogen/n-hexane ratio promoted metal catalyzed skeletal isomerization, mainly by the C5-cyclic pathway and shifted also the fragment composition towards vmues typical of metal-catalyzed hydrogenolysis. 

In order to reduce the reaction temperature of acid catalyzed alkane conversion reactions one can reduce the temperature by replacing carbonium formation by a route via the carbenium ion by protonation of alkenes generated by metal-catalyzed (group 8-10 metals, e.g. Ft, Pd) dehydrogenation of alkanes. The metals can be readily dispersed in the micropores of a zeolite. A lowering of the reaction temperature is especially useful for alkane isomerization. A low temperature favours the branched product and inhibits consecutive reactions. 

Medium pore aluminophosphate based molecular sieves with the -11, -31 and -41 crystal structures are active and selective catalysts for 1-hexene isomerization, hexane dehydrocyclization and Cg aromatic reactions. With olefin feeds, they promote isomerization with little loss to competing hydride transfer and cracking reactions. With Cg aromatics, they effectively catalyze xylene isomerization and ethylbenzene disproportionation at very low xylene loss. As acid components in bifunctional catalysts, they are selective for paraffin and cycloparaffin isomerization with low cracking activity. In these reactions the medium pore aluminophosphate based sieves are generally less active but significantly more selective than the medium pore zeolites. Similarity with medium pore zeolites is displayed by an outstanding resistance to coke induced deactivation and by a variety of shape selective actions in catalysis. The excellent selectivities observed with medium pore aluminophosphate based sieves is attributed to a unique combination of mild acidity and shape selectivity. Selectivity is also enhanced by the presence of transition metal framework constituents such as cobalt and manganese which may exert a chemical influence on reaction intermediates. 

Typical reaction in this category is the conversion of limonene to P-cymene over Pd-H-borosilicalite where isomerization is followed by dehydrogenation. Also many reactions mentioned here, particularly catalyzed by transition metal ion or bimeallic, are bifunctional zeolitic reactions. 

The catalytic activity of alkali metal oxide clusters encapsulated in the zeolitic cages of faujasite has been tested in different reactions catalyzed by basic sites, e. g. olefin isomerization [75,77], isopropanol decomposition [67,68], and Knoe-venagel condensation [73,74,78]. 

Baba et al. prepared low-valent lanthanide species introduced into zeolite by impregnation from Y and Eu metals dissolved in liquid ammonia followed by evacuation at 773 K[46]. The resulting compounds catalyzed 1-butene isomerization by anionic mechanisms. TPD results with the catalysts suggest that metal imides such as EuNH act as basic sites. 

In this paper, pyridine adsorption was utilized to investigate the hydrogen spillover phenomenon from metal to acidic centers of zeolite by observing hydrogenation of chemisorbed pyridine on B or L acid sites of USY zeolite using hybrid catalyst composed of USY zeolite and Pt/SiOo. To give insight into spill-over process in the hybrid catalyst system, isomerization of n-pentane, which is one of the typical add catalyzed reaction, was also studied. 

Platinum (metal)- and acid (oxide)-catalyzed processes were developed to convert petroleum to high-octane fuels. Hydrodesulfurization catalysis removed sulfur from the crude to prevent catalyst deactivation. The discovery of microporous crystalline alumina silicates (zeolites) provided more selective and active catalysts for many reactions, including cracking, hydrocracking, alkylation, isomerization, and oligomerization. Catalysts that polymerize ethylene, propylene, and other molecules were discovered. A new generation of bimetallic catalysts that were dispersed on high-surface-area (100-400 m /g) oxides was synthesized. 

Heterogeneous metal oxides also catalyze the isomerization of alkyl-benzenes, for example, under the action of H-ZSM-5 zeolite at 723 K 1,2,4-tri-methylbenzene is transformed into 1,2,3- and 1,3,5-trymethylbenzenes [16]. 

Carbanions as intermediates have been suggested in the base-catalyzed isomerization of imsaturated nitriles. As long as zeolites with anion-exchange properties are not available, basic centers must be introduced by exchange of the nonframework ions by alkali metal ions or of silicon by germanium, by precipitation... 

The bifunctionality of metal-doped zeolite catalysts is explained here for the important example of isomerization and hydrogenation. The metal content facilitates the hydrogenation and dehydrogenation steps, while the acid-catalyzed isomerization step takes place under the restricted conditions of the zeolite cavities (Scheme 7-1). 

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