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US4540831A Expired / Lapsed US ⏱️ 0.0 years remaining

Mixed-phase hydrocarbon conversion process employing total overhead condenser

Assignee: Honeywell UOP LLC
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Filing: 1984-05-17
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Granted: 1985-09-10
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Expires: 2004-05-17
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Abstract

Abstract A process is disclosed for performing an exothermic reaction such as the etherification of isobutylene with methanol. The feed is charged to a vertical reaction zone containing a solid catalyst. Heat released by the exothermic reaction partially vaporizes the reactants, with the vapors traveling upward to a condensing zone. All of the condensable vapors entering the condensing zone are condensed and returned downward to the catalyst bed. A single effluent stream made up of the product, excess reactants and any unreactive compounds present in the feed streams is removed from the bottom of the reaction zone. This total reflux reaction zone allows temperature control within a catalyst bed without the use of indirect heat exchangers located within the reaction zone.

Inventors

  • 👤 Bruce A. Briggs

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-01 05:29
CPC Classifications
B; B01; B01J; B01J8/00; B01J8/02; B01J8/04; B01J8/0446; B01J8/0449; B01J8/0453; B01J8/0496; C; C07; C07C; C07C41/00; C07C41/01; C07C41/05; C07C41/06; B01J2208/00; B01J2208/00008; B01J2208/00017; B01J2208/00106; B01J2208/00168; B01J2208/00194; Y; Y10; Y10S; Y10S203/00; Y10S203/06

Claims Analysis

Total Claims: 12
Claim 1
Independent Claim 274 words
An exothermic etherification process for the continuous reaction of an olefinic hydrocarbon having less than six carbon atoms per molecule with an alcohol which comprises the steps of: (a) passing said olefinic hydrocarbon and said alcohol into a reaction zone maintained at reaction-promoting conditions and containing a solid etherification catalyst which promotes said exothermic etherification between said olefinic hydrocarbon and said alcohol to form a corresponding ether compound which is less volatile than said alcohol and said olefinic hydrocarbon, and with a vapor phase being forward within the reaction zone at least in part by the vaporization of said alcohol, olefinic hydrocarbon or both, said alcohol and olefinic hydrocarbon vaporized as a result of heat released in said exothermic reaction; (b) condensing substantially all of the condensible vapor in said vapor phase in an upper portion of said reaction zone by indirect heat exchange with a fluid of lower temperature than said vapor phase to form a condensate liquid phase containing substantially all of said condensibles present in the vapor phase including both reactants comprising said olefinic hydrocarbon and said alcohol in liquid phase; (c) passing downwardly through the reaction zone from a point elevated with respect to the etherification catalyst all of said condensate liquid phase including both said reactant within said reaction zone; (d) removing said formed ether compounds as a liquid phase effluent stream from a bottom portion of said reaction zone in accompaniment with substantially all of said alcohol and olefinic hydrocarbon added to said reaction zone in step (a) and not consumed in said etherification reaction zone; and (e) recovering said ether compound from said liquid phase effluent stream.
Claim 2
Dependent Claim 274 words
An exothermic etherification process for the continuous reaction of an olefinic hydrocarbon having less than six carbon atoms per molecule with an alcohol which comprises the steps of: (a) passing said olefinic hydrocarbon and said alcohol into a reaction zone maintained at reaction-promoting conditions and containing a solid etherification catalyst which promotes said exothermic etherification between said olefinic hydrocarbon and said alcohol to form a corresponding ether compound which is less volatile than said alcohol and said olefinic hydrocarbon, and with a vapor phase being forward within the reaction zone at least in part by the vaporization of said alcohol, olefinic hydrocarbon or both, said alcohol and olefinic hydrocarbon vaporized as a result of heat released in said exothermic reaction; (b) condensing substantially all of the condensible vapor in said vapor phase in an upper portion of said reaction zone by indirect heat exchange with a fluid of lower temperature than said vapor phase to form a condensate liquid phase containing substantially all of said condensibles present in the vapor phase including both reactants comprising said olefinic hydrocarbon and said alcohol in liquid phase; (c) passing downwardly through the reaction zone from a point elevated with respect to the etherification catalyst all of said condensate liquid phase including both said reactant within said reaction zone; (d) removing said formed ether compounds as a liquid phase effluent stream from a bottom portion of said reaction zone in accompaniment with substantially all of said alcohol and olefinic hydrocarbon added to said reaction zone in step (a) and not consumed in said etherification reaction zone; and (e) recovering said ether compound from said liquid phase effluent stream.
Claim 3
Dependent Claim 14 words
The process of claim 1 further characterized in that the olefinic hydrocarbon is isobutylene.
Claim 4
Dependent Claim 16 words
The process of claim 2 further characterized in that the etherification catalyst comprises an acidic resin.
Claim 5
Dependent Claim 46 words
The process of claim 2 further characterized in that isobutylene is charged to the reaction zone in admixture with at least one other C 4 hydrocarbon, and in that said other C 4 hydrocarbon is removed from the reaction zone as part of the effluent stream.
Claim 6
Dependent Claim 235 words
An exothermic etherification process for the continuous reaction of olefinic hydrocarbons having four carbon atoms per molecule with an alcohol, which comprises the steps of: (a) passing said olefinic hydrocarbon and said alcohol into a reaction zone maintained at reaction-promoting conditions and containing a bed of solid etherification catalyst which promotes said exothermic etherification between said olefinic hydrocarbon and said alcohol to form a corresponding ether compound which is less volatile than said alcohol and said olefinic hydrocarbon, and with a vapor being formed within said reaction zone at least in part by the vaporization of said olefinic hydrocarbon and said alcohol by heat released in said exothermic reaction; (b) passing said vapor phase containing both alcohol and olefinic compound into a condensing zone located above the bed of said etherification catalyst to form a condensate stream by condensing essentially all of said condensible compounds, including said alcohol and olefinic hydrocarbon, present in said vapor phase stream; (c) passing all of said condensate including both of said reactants, downward into said bed of solid etherification catalyst from a position elevated with respect to said bed of etherification catalyst; (d) withdrawing a liquid phase effluent stream which comprises said ether compound in accompaniment with all of said alcohol and olefinic hydrocarbon not consumed within said reaction zone from a bottom portion of said reaction zone; and (e) recovering said ether product from said bottoms effluent stream.
Claim 7
Dependent Claim 235 words
An exothermic etherification process for the continuous reaction of olefinic hydrocarbons having four carbon atoms per molecule with an alcohol, which comprises the steps of: (a) passing said olefinic hydrocarbon and said alcohol into a reaction zone maintained at reaction-promoting conditions and containing a bed of solid etherification catalyst which promotes said exothermic etherification between said olefinic hydrocarbon and said alcohol to form a corresponding ether compound which is less volatile than said alcohol and said olefinic hydrocarbon, and with a vapor being formed within said reaction zone at least in part by the vaporization of said olefinic hydrocarbon and said alcohol by heat released in said exothermic reaction; (b) passing said vapor phase containing both alcohol and olefinic compound into a condensing zone located above the bed of said etherification catalyst to form a condensate stream by condensing essentially all of said condensible compounds, including said alcohol and olefinic hydrocarbon, present in said vapor phase stream; (c) passing all of said condensate including both of said reactants, downward into said bed of solid etherification catalyst from a position elevated with respect to said bed of etherification catalyst; (d) withdrawing a liquid phase effluent stream which comprises said ether compound in accompaniment with all of said alcohol and olefinic hydrocarbon not consumed within said reaction zone from a bottom portion of said reaction zone; and (e) recovering said ether product from said bottoms effluent stream.
Claim 8
Dependent Claim 16 words
The process of claim 5 further characterized in that the C 4 olefinic hydrocarbon is isobutylene.
Claim 9
Dependent Claim 68 words
The process of claim 6 further characterized in that isobutylene is charged to the reaction zone in admixture with at least one other C 4 hydrocarbon, which is not significantly consumed in said reaction, and in that substantially all of the C 4 hydrocarbons other than isobutylene which enter the reaction zone are withdrawn from the reaction zone as a portion of the effluent stream in step (d).
Claim 10
Dependent Claim 13 words
The process of claim 5 further characterized in that the alcohol is methanol.
Claim 11
Dependent Claim 26 words
The process of claim 5 further characterized in that the condensing zone is not located in the same process vessel as the bed of solid catalyst.
Claim 12
Dependent Claim 18 words
The process of claim 5 further characterized in that the solid etherification catalyst comprises an acidic ion-exchange resin.

References Cited (Backward Citations)

US2373501A Cited
US3989762A Cited
US3824289A Cited
US4281206A Cited
US4087471A Cited
US4232177A Cited
US4475005A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-09-09 1989-03-11 1989-09-10 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-09-09 1993-03-11 1993-09-10 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-09-09 1997-03-11 1997-09-10 $7700.00 Window Closed / Lapsed

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