Hydroalkylation of aromatic hydrocarbons

Chemistry of hydrocarbon compounds – Adding hydrogen to unsaturated bond of hydrocarbon – i.e.,... – Hydrocarbon is aromatic

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C585S270000, C585S268000, C585S427000, C585S467000

Reexamination Certificate

active

06506953

ABSTRACT:

FIELD OF INVENTION
This invention relates to a process for the hydroalkylation of aromatic compounds and particularly to a process for the hydroalkylation of benzene to produce cyclohexylbenzene.
BACKGROUND TO THE INVENTION
Cyclohexylbenzene can be used to produce phenol, which is one of the most important industrial chemicals in the world. As of December 1995, more than 88% of world phenol capacity was based on cumene peroxidation with acetone coproduction. One of the primary economic difficulties of the cumene peroxidation route is that it requires the existence of an available market for the co-produced acetone. Currently, the growth of market demand for phenol exceeds that for acetone, and hence there exists an acetone oversupply problem. It is expected that this unbalanced growth will continue for some time.
Hydroperoxidation of cyclohexylbenzene (analogous to cumene peroxidation) could offer an alternative route for phenol production without the problem of acetone co-production. This alternative route co-produces cyclohexanone, which is a much more valuable and desirable by-product than acetone. Thus cyclohexanone is useful for the manufacture of caprolactam and nylon.
Dehydrogenation of cyclohexylbenzene also offers a low cost alternative to produce diphenyl from benzene. Diphenyl is used mainly for heat-transfer applications. Currently the main source of diphenyl is as a by-product (1 g diphenyl/100 g benzene) in benzene production by toluene dealkylation. The crude diphenyl is refined to 93-97% purity by distillation. High purity diphenyl can also be produced by direct thermal dehydrocondensation of benzene at 700-800° C. in gas or electrically heated tubular reactors. This process is energy intensive and produces by-products of terphenyl, higher polyphenyls and tars.
It is known that cyclohexylbenzene can be produced from benzene by the process of hydroalkylation or reductive alkylation. In this process, benzene is heated with hydrogen in the presence of a catalyst such that the benzene undergoes partial hydrogenation to produce cyclohexene which then alkylates the benzene starting material. Thus U.S. Pat. Nos. 4,094,918 and 4,177,165 disclose hydroalkylation of aromatic hydrocarbons over catalysts which comprise nickel- and rare earth-treated zeolites and a palladium promoter. Similarly, U.S. Pat. Nos. 4,122,125 and 4,206,082 disclose the use of ruthenium and nickel compounds supported on rare earth-treated zeolites as aromatic hydroalkylation catalysts. The zeolites employed in these prior art processes are zeolites X and Y. More recently, U.S. Pat. No. 5,053,571 has proposed the use of ruthenium and nickel supported on zeolite beta as an aromatic hydroalkylation catalyst.
It has now been found that the recently discovered zeolite designated MCM-68, when combined with a hydrogenation metal, has activity for the hydroalkylation of aromatic hydrocarbons to produce cycloalkyl-substituted aromatic compounds, such as cyclohexylbenzene.
SUMMARY OF THE INVENTION
According to one aspect of the invention there is provided a process for the hydroalkylation of an aromatic hydrocarbon comprising the step of contacting the aromatic hydrocarbon with hydrogen in the presence of a catalyst comprising a first metal having hydrogenation activity and a porous crystalline material, MCM-68, which contains at least one channel system, in which each channel is defined by a 12-membered ring of tetrahedrally coordinated atoms, and at least two further, independent channel systems, in each of which each channel is defined by a 10-membered ring of tetrahedrally coordinated atoms, wherein the number of unique 10-membered ring channels is twice the number of 12-membered ring channels.
Preferably, the aromatic hydrocarbon is benzene.
Preferably, the first metal is selected from palladium, ruthenium, nickel and cobalt.
Preferably, the catalyst also contains a second metal, different from the first metal, and selected from zinc, tin, nickel and cobalt.


REFERENCES:
patent: 3354078 (1967-11-01), Miale et al.
patent: 4094918 (1978-06-01), Murtha et al.
patent: 4118434 (1978-10-01), Murtha et al.
patent: 4122125 (1978-10-01), Murtha et al.
patent: 4177165 (1979-12-01), Murtha et al.
patent: 4206082 (1980-06-01), Murtha et al.
patent: 4219687 (1980-08-01), Dolhyj et al.
patent: 4219689 (1980-08-01), Murtha
patent: 5053571 (1991-10-01), Makkee
patent: 6049018 (2000-04-01), Calabro et al.
patent: 0 006 401 (1978-06-01), None
patent: 0 002 824 (1978-12-01), None
patent: 1184022 (1969-02-01), None
patent: 00/43316 (2000-07-01), None
Journal of Catalysts 4, pp. 527-529 (1965), Superactive Crystalline Aluminosilicate Hydrocarbon Catalysts, P.B. Weisz and J.N. Maile.
Journal of Catalysts 6, pp. 278-287 (1966), Catalysts by Crystalline Aluminosilicates IV. Attainable Catalytic Cracking Rate Constants, and Superactivity, J.N. Miale, N.Y. Chen and P.B. Weisz.
Journal of Catalysts 61, pp. 390-396 (1980), Chemical and Physical Properties of the ZSM-5 Substitutional Series, D.H. Olsen, W.O. Haag and R.M. Lago.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Hydroalkylation of aromatic hydrocarbons does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Hydroalkylation of aromatic hydrocarbons, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Hydroalkylation of aromatic hydrocarbons will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-3054608

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.