Transport hydroxylation reactor

Organic compounds -- part of the class 532-570 series – Organic compounds – Oxygen containing

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568800, C07C 3760

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active

058921320

ABSTRACT:
A continuous process for converting benzene or a derivative thereof to phenol or a derivative thereof comprises continuously activating .alpha.-sites on a zeolite catalyst by contacting the catalyst with a free oxidant activator, thereby producing an activated zeolite hydroxylation catalyst, and separately and continuously contacting benzene or a derivative thereof with the activated zeolite catalyst, thereby producing phenol or a derivative thereof. The benzene or derivative thereof can be separately contacted with the activated zeolite catalyst by (a) contacting in a reaction vessel that is physically separate and distinct from the vessel in which the catalyst is contacted with the free oxidant activator, (b) contacting in a zone of a vessel that is separate from the zone in that same vessel in which the catalyst is contacted with the free oxidant activator, or (c) contacting with the catalyst in a reaction vessel in a first time pulse, with the benzene or derivative thereof being contacted with the activated zeolite catalyst in a second time pulse in the same reaction vessel which does not overlap substantially with the first time pulse.

REFERENCES:
patent: 4258222 (1981-03-01), Mohring et al.
patent: 4982013 (1991-01-01), Gubelmann et al.
patent: 5001280 (1991-03-01), Gubelmann et al.
patent: 5019657 (1991-05-01), Gubelmann et al.
patent: 5055623 (1991-10-01), Gubelmann et al.
patent: 5110995 (1992-05-01), Kharitonov et al.
patent: 5171553 (1992-12-01), Li et al.
patent: 5502259 (1996-03-01), Zakoshansky et al.
Dvorak et al. (1970) Determination Of The Specific Copper Surface Area By Chromatographic Technique; Journal of Catalysis 18, 108-114, Academic Press, Inc.
Evans et al. (1983) On The Determination Of Copper Surface Area By Reaction With Nitrous Oxide; Applied Catalysis 7, 75-83, Elsevier Science Publishers B.V.
Iwamoto et al. (1983) Catalytic Oxidation By Oxide Radical Ions. 1. One-Step Hydroxylation Of Benzene To Phenol Over Group 5 And 6 Oxides Supported On Silica Gel; The Journal of Physical Chemistry 87, No. 6, The American Chemical Society.
Ono et al. (1988) Functionalization Of Benzene By Its Reaction With Nitrogen Oxides Over Solid-Acid Catalysts, Heterogeneous Catalysis and Fine Chemicals pp. 75-82, Elsevier Science Publishers B.V., Amsterdam.
Suzuki et al. (1988) Hydroxylation Of Benzene With Dinitrogen Monoxide Over H-ZSM-5 Zeolite, Chemistry Letters pp. 953-956, The Chemical Society of Japan.
Panov et al. (1990) The Role Of Iron In N.sub.2 O Decomposition On ZSM-5 Zeolite And Reactivity Of The Surface Oxygen Formed, Journal of Molecular Catalysis 61, 85-97, Elsevier Sequoia.
Sobolev et al. (1991) Anomalously Low Bond Energy Of Surface Oxygen On FeZSM-5 Zeolite, Mendeleev Communications, No. 1, pp. 29-30.
Zholobenko (1993) Preparation Of Phenol Over Dehydroxylated HZSM-5 Zeolites, Mendeleev Communications, pp. 23-24.
Hafele et al. (1996) Hydroxylation of Benzene on ZSM5 Type Catalysts, DGMK-Conference, Catalysis On Solid Acids And Bases pp. 243-251.
Vereshchagin et al, Conversion Of Ethane On Zeolite Catalysts In The Presence Of Oxygen And Nitrogen(I) Ox De, Izv. Akad. Nauk SSSR, (1988), 1718-1722 The enclosed is an English abstract translated from a Russian article.
Li et al. (1992) Catalytic Decomposition Of Nitrous Oxide On Metal Exchanged Zeolites; Applied Catalysis B: Environmental 1, L21-29; Elsevier Science Publishers B.V., Amsterdam.
Sobolev et al. (1993) Catalytic Properties Of ZSM-5 Zeolites In N.sub.2 O Decomposition: The Role Of Iron; Journal of Catalysis 139, 435-443; Academic Press, Inc.
Sobolev et al. (1993) Stoichiometric Reaction Of Benzene With .alpha.-Form Of Oxygen On Fezsm-5 Zeolites. Mechanism Of Aromatics Hydroxylation By N.sub.2 O; Journal of Molecular Catalysis 84, 117-124; Elsevier Science Publishers B.V., Amsterdam.
Panov et al. (1992) Oxidation Of Benzene To Phenol By Nitrous Oxide Over Fe-ZSM-5 Zeolites; Applied Catalysis A: General 82, 31-36, Elsevier Science Publishers B.V., Amsterdam.
Kharitonov et al. (1993) Ferrisilcate Analogs Of ZSM-5 Zeolite As Catalysts For One Step Oxidation Of Benzene To Phenol; Applied Catalysis A: General 98, 33-43, Elsevier Science Publshers B.V., Amsterdam.
Burch et al. (1993) Factors Affecting The Deactivation Of Various Zeolites Used As Catalysts For The Direct Partial Oxidation Of Benzene To Phenol; Applied Catalysis A: General 106, 167-183, Elsevier Science Publishers B.V., Amsterdam.
Burch et al. (1993) Investigation Of Zeolite Catalysts For The Direct Parial Oxidation Of Benzene To Phenol; Applied Catalysis A: General 103, 135-162, Elsevier Science Publishers B.V., Amsterdam.
Burch et al. (1993) Direct Partial Oxidation Of Benzene To Phenol on Zeolite Catalysts; Applied Catlysis A: General 86, 139-146, Elsevier Science Publishers B.V., Amsterdam.
Panov et al. (1993) Oxidative Hydroxylation Using Dinitrogen Monoxide; A Possible Route For Organic Synthesis Over Zeolites, Applied Catalysis A: General, 98, 1-20, Elsevier Science Publishers B.V., Amsterdam.
Derwent abstract; JP 5 009 142.
Derwent abstract, JP 4 334 333.
Derwent abstract, JP 4 021 645.
Derwent abstract, JP 6 009 464.
Derwent abstract, JP 6 040 976.
Derwent abstract, EP 406 050.

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