Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Vapor-phase Beckmann rearrangement

As already discussed in Chapter 1, the commercialization, by Sumitomo [GO-64], of a vapor phase Beckmann rearrangement of cyclohexanone oxime to caprolactam over a high-silica MFI (ZSM-5 type) zeolite (Fig. 2.21) is another benchmark in zeolite catalysis. The process, which currently operates on a 90000 tpa scale, replaces a conventional one employing stoichiometric quantities of sulfuric acid and producing ca. 2 kg of ammonium sulfate per kg of caprolactam. [Pg.67]

Most of the catalytic activity of zeolites has been concerned with their ability to act as shape selective solid acids. The vapor phase Beckmann rearrangement of cyclohexanone oxime over HY zeolite at 300°C gave caprolactam in 80% selectivity at 82% conversion (Eqn. 10.22). 5... [Pg.204]

Although many solid-acid catalysts have been reported for the vapor-phase Beckmann rearrangement [2], their performance has been less than satisfactory from an industrial standpoint and the heterogeneously catalyzed Beckmann rearrangement has not yet been commercialized. In this chapter heterogeneous catalysis of the Beckmann rearrangement, its mechanism, and acid properties and reaction conditions suitable for the reaction will be reviewed. [Pg.185]

Table 1. Product distribution in vapor-phase Beckmann rearrangement reactions ... [Pg.190]

Figure 5. Change in cyclohexanone oxime conversion and lactam selectivity with time on stream in the vapor phase Beckmann rearrangement over 12-MR zeolites. Diluent (a) methanol, (b) 1-hexanol. (X) H-BEA, (A) H-LTL, (V) H-OFF-ERI, ( ) H-USY (Si02/Al203 = 62), (O) H-MOR, (O) H-MTW 623 K, oxime/diluent/N, molar ratio of 1/9/5.9 and W/F of 80 g cat h mol oxime [41]. Figure 5. Change in cyclohexanone oxime conversion and lactam selectivity with time on stream in the vapor phase Beckmann rearrangement over 12-MR zeolites. Diluent (a) methanol, (b) 1-hexanol. (X) H-BEA, (A) H-LTL, (V) H-OFF-ERI, ( ) H-USY (Si02/Al203 = 62), (O) H-MOR, (O) H-MTW 623 K, oxime/diluent/N, molar ratio of 1/9/5.9 and W/F of 80 g cat h mol oxime [41].
The control of selectivity in the vapor phase Beckmann rearrangement seems to be difficult this can be ascribed to the drastic experimental conditions required. Liquid-phase reactions over heterogeneous catalysts have been investigated. The Beckmann rearrangement of cyclohexanone oxime in the liquid phase was performed under reflux conditions in a variety of solvents [44]. When chlorobenzene was used solvent conversion and selectivity increased with temperature up to 405 K. From plots of conversion against time it was concluded that catalyst deactivation under liquid-phase conditions is small, in contrast with the rapid deactivation observed when the reaction was conducted in the vapor phase. [Pg.200]

AlP04-Ti02 catalysts. V. Vapor-phase Beckmann rearrangement of cyclohexanone oxime... [Pg.615]

Vapor-phase Beckmann rearrangement of cyclohexanone oxime over AIPO4 (AP) and AlP04-Ti02 (APTi, 25-75 wt%) catalysts was investigated. Apparent rate constants and activation parameters were calculated in terms of the kinetic model of Bassett and Habgood for first order reaction processes. In all cases the selectivity to e-caprolactam increased with reaction temperature and,... [Pg.615]

P-16 - Effect of oxygen concentration on catalyst deactivation rate in vapor phase Beckmann rearrangement over acid catalysts... [Pg.368]

Shouro, D., Moriya, Y, Nakajima, T., and Mishima, S. 2000. Mesoporous silica ESM-16 catalysts modified with various oxides for the vapor-phase Beckmann rearrangement of cyclohexanone oxime. App/. Catal. A.- Gen. 198 275-282. [Pg.991]

FIGURE 9.23. Sumitomo process combined ammoximation and vapor phase Beckmann rearrangement for caprolactam synthesis. [Pg.269]

Mesoporous silica FSM-16 catalysts modified with various oxides were used in the vapor-phase Beckmann rearrangement of The selective formation of the lactam 6 was improved by using FSM-16 supported by AI2O3, ZnO and CdO. [Pg.277]

A novel super-microporous layered material, silica-pillared niobic acid, was prepared by a guest-exchange route. This pillard material was found to be an acid catalyst for the vapor-phase Beckmann rearrangement of 5 to 6 in 1-hexanol, which exhibited a 100% conversion of the oxime with a selectivity of lactam above 85% at 340 °C. ... [Pg.277]

The influence of different post-synthesis modifications on the catalytic performances of p-silicates in the vapor-phase Beckmann rearrangement of 5 to 6 was examined by Fomi et al. ... [Pg.277]

Ichihashi, H. and Kitamura, M. (2002). Some Aspects of the Vapor Phase Beckmann Rearrangement for the Production of e-Caprolactam over High Silica MFI Zeolites, Catal. Today, 73, pp. 23-28. [Pg.378]

H. Ichihashi, M. Ishida, A. Shiga, M. Kitamura, T. Suzuki, K. Suenobu, K. Sugitaet al.. The catalysis of vapor-phase Beckmann rearrangement forthe production of e-caprolactam. Catal. Surv. Asia. 7, 261-270 (2003)... [Pg.379]


See other pages where Vapor-phase Beckmann rearrangement is mentioned: [Pg.193]    [Pg.12]    [Pg.234]    [Pg.368]    [Pg.276]    [Pg.277]    [Pg.277]    [Pg.278]   


SEARCH



Beckmann rearrangement vapor-phase cyclohexanone oxime

Beckmann rearrangment

Beckmann vapor phase

© 2024 chempedia.info