Tetralin dehydrogenation

In contrast, a catalytic reaction pair of tetralin dehydrogenation/naphthalene hydrogenation (Equation 13.3) is another choice for stationary applications. Although the storage densities of tetralin are relatively low (3.0 wt%, 28.2 kg-H2/m3), rates of absorbing and desorbing hydrogen... 

To examine the catalyst deterioration under the present superheated liquid-film conditions, a long-term tetralin dehydrogenation over the carbon-supported platinum catalyst (Pt/C) was carried out under the superheated liquid-film conditions (heating temperature 240°C) at the amount ratio of 1.1 g/0.5 mL/min [13]. Figure 13.21 shows the time courses of reaction rate and conversion in the tetralin dehydrogenation. High conversion (around 50%) was maintained for longer than 5 h. 

Tetrachloroethane, purification of, 176 Tetradecanoic acid, 938, 940, 941 n-Tetradecyl bromide, 283 1 2 3 4-Tetrahydrocarbazole, 852 Tetrahydrofuran, 271 Tetrahydrofurfuryl chloride, 896, 901 Tetrahydropyran, 271 Tetralin, dehydrogenation of, 948, 949 purification of, 949 a-Tetralone, 728, 737 Tetramethyl base, 987 pp -Tetramethyldiaminodiphenyl-methane, 987... 

Dehydrogenation activity has been demonstrated for Rh, Co, and Ni forms of zeolites X and Y (123-125), Both cyclohexane and tetralin dehydrogenation to benzene and naphthalene, respectively, have been used as test reactions. For NiX zeolites, unreduced Ni2 + ions were considered (124) to be the active centers. The incorporation of Ca2+ ions into the zeolite... 

The most important process to produce 1-naphthalenol was developed by Union Carbide and subsequently sold to Rhc ne-Poulenc. It is the oxidation of tetralin, l,2,3,4-tetrahydronaphthalene/719-64-2] in the presence of a transition-metal catalyst, presumably to l-tetralol—1-tetralone by way of the 1-hydroperoxide, and dehydrogenation of the intermediate ie, l-tetralol to 1-tetralone and aromatization of 1-tetralone to 1-naphthalenol, using a noble-metal catalyst (58). 1-Naphthol production in the Western world is around 15 x 10 t/yr, with the United States as the largest producer (52). 

The catalytic system used in the Pacol process is either platinum or platinum/ rhenium-doped aluminum oxide which is partially poisoned with tin or sulfur and alkalinized with an alkali base. The latter modification of the catalyst system hinders the formation of large quantities of diolefins and aromatics. The activities of the UOP in the area of catalyst development led to the documentation of 29 patents between 1970 and 1987 (Table 6). Contact DeH-5, used between 1970 and 1982, already produced good results. The reaction product consisted of about 90% /z-monoolefins. On account of the not inconsiderable content of byproducts (4% diolefins and 3% aromatics) and the relatively short lifetime, the economics of the contact had to be improved. Each diolefin molecule binds in the alkylation two benzene molecules to form di-phenylalkanes or rearranges with the benzene to indane and tetralin derivatives the aromatics, formed during the dehydrogenation, also rearrange to form undesirable byproducts. 

For small scale dehydrogenations, the apparatus shown in Fig. VI, 35, 1 may be us. Place 2-5 g. of puri ed tetralin (1) and 0-25 g. of palladised charcoal in thec -c z apparatus and heat to boiling for 4 hours in a slow current of dry carbon dioxide. 

Tetralin has been shown to undergo thermal dehydrogenation to naphthalene and rearrangement to methyl indan in either the absence or presence of free radical acceptors [ 1, 2]. The presence of free radical acceptors usually accelerates the rearrangement reaction. Even with alkylated Tetralins>... 

Sym-octahydrophenanthrene (HgPh) would be expected to follow the same rearrangement-dehydrogenation reactions as Tetralin, except with more isomer and product possibilities. The reactions shown in Figure 1 illustrate the many structures expected from sym-HgPh in the presence of free radical acceptors. Unlike Tetralin, hydrophenanthrenes have multiple structures which each, in turn, form various isomers. The amounts of these isomers are dependent upon the type of hydrogen-transfer reactions and the environment of the system. 

Catalytic Dehydrogenation of Tetralin over Carbon-Supported Platinum Nanoparticles under Superheated Liquid-Film... 

In the adequate case (1.0 or 2.0 mL tetralin), the catalyst appeared to be wet differently from dry sand-bath or suspension states. As in the case of decalin dehydrogenation under the superheated liquid-film conditions, the catalyst temperature is higher than the boiling point, exhibiting a temperature gradient, and the substrate liquid is limited in amount to... 

Dehydrogenation Activities for Decalin and Tetralin under Superheated Liquid-Film Conditions... 

Dehydrogenation activities, compared for tetralin and decalin [5,12] under the same superheated liquid-film conditions over the same Pt/C catalyst, exhibited around 3.9-63 times preference of tetralin (Table 13.3), which can certainly be ascribed to advantageous adsorption due to the a-bonding capability of its aromatic part [17-19]. It was, thus, confirmed experimentally that tetralin is superior to decalin as the organic hydrogen carrier for stationary applications in terms of rapid hydrogen supply or power density, provided that the density of fuel storage is unimportant. 

Time courses of dehydrogenation activities with carbon-supported platinum catalyst under superheated liquid-film conditions in laboratory-scale continuous operation. Catalyst platinum nanoparticles supported on granular activated carbon (Pt/C, 5 wt-metal%), 1.1 g. Feed rate of tetralin 0.5 mL/min (superheated liquid-film conditions). Reaction conditions boiling and refluxing by heating at 240°C and cooling at 25°C. (Reproduced from Hodoshima, Sv Shono, A., Satoh, Kv and Saito, Yv Chem. Eng. Trans8,183-188, 2005. With permission.)... 

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