U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Moving bed hydrocarbon conversion process

Patent 5157181 Issued on October 20, 1992. Estimated Expiration Date: Icon_subject December 3, 2010. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

2659758

3838039

Production of light olefins
Patent #: 4499327
Issued on: 02/12/1985
Inventor: Kaiser

Regeneration method with reduced catalyst heat exposure
Patent #: 4859643
Issued on: 08/22/1989
Inventor: Sechrist ,   et al.

Chemical conversion process
Patent #: 4873390
Issued on: 10/10/1989
Inventor: Lewis, et al.

Conversion of alkanes to gasoline
Patent #: 4879424
Issued on: 11/07/1989
Inventor: Harandi

Multistage process for converting oxygenates to liquid hydrocarbons and ethene Patent #: 4929780
Issued on: 05/29/1990
Inventor: Wright, et al.

Inventors

Assignee

Application

No. 621692 filed on 12/03/1990

US Classes:

585/329, Including polymerization of olefin585/640Using metal oxide catalyst

Examiners

Primary: Garvin, Patrick P.
Assistant: Irzinski, E. D.

Attorney, Agent or Firm

Foreign Patent References

  • 0071437 EP. 02/24/1983
  • 0230792 DE. 12/24/1985

International Class

C07C 001/00

Abstract

Moving bed hydrocarbon conversion processes are disclosed wherein a carbonaceous material is deposited on a solid catalyst used in the conversion process to form a coked catalyst which is regenerated in a regeneration zone in order to remove the carbonaceous deposit material from the catalyst and provide a regenerated catalyst having an increased number of active catalyst sites relative to the coked catalyst. The regenerated catalyst is then added to the reaction zone at a rate effective to enhance the conversion to desired products without enhancing the conversion to undesired by-products. When a radial flow reaction zone is employed a relatively constant amount of active catalyst sites can be maintained through the reaction zone by increasing the thickness of annulus through which the catalyst flows in the lower section of the reaction zone wherein the catalyst is more severely coked and has fewer active catalyst sites. The conversion of aliphatic hetero compounds, such as methanol to produce olefins in the C2 -C4 carbon range is specifically exemplified.

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