US2660520A - Apparatus for catalytic conversion of hydrocarbons - Google Patents

Apparatus for catalytic conversion of hydrocarbons Download PDF

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US2660520A
US2660520A US289132A US28913252A US2660520A US 2660520 A US2660520 A US 2660520A US 289132 A US289132 A US 289132A US 28913252 A US28913252 A US 28913252A US 2660520 A US2660520 A US 2660520A
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phosphoric acid
liner
copper
vessel
hydrocarbons
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US289132A
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Sam R Bethea
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Standard Oil Development Co
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Standard Oil Development Co
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/0242Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid flow within the bed being predominantly vertical
    • B01J8/025Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid flow within the bed being predominantly vertical in a cylindrical shaped bed
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/02Apparatus characterised by being constructed of material selected for its chemically-resistant properties
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/008Details of the reactor or of the particulate material; Processes to increase or to retard the rate of reaction
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/00477Controlling the temperature by thermal insulation means
    • B01J2208/00495Controlling the temperature by thermal insulation means using insulating materials or refractories
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/02Apparatus characterised by their chemically-resistant properties
    • B01J2219/0204Apparatus characterised by their chemically-resistant properties comprising coatings on the surfaces in direct contact with the reactive components
    • B01J2219/0227Apparatus characterised by their chemically-resistant properties comprising coatings on the surfaces in direct contact with the reactive components of graphite
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/02Apparatus characterised by their chemically-resistant properties
    • B01J2219/0204Apparatus characterised by their chemically-resistant properties comprising coatings on the surfaces in direct contact with the reactive components
    • B01J2219/0236Metal based

Definitions

  • the present invention is directed to a method and apparatus for converting hydrocarbons. More particularly, the invention is directed to the catalytic conversion of a convertible hydrocarbon feed including an olefin. The invention is specifically directed to polymerization of olefins.
  • the present invention may be described brieily as involving the catalytic conversion of a convertible hydrocarbon including an olefin such as polymerization of a mono-olefin having from 2 to 6 carbon atoms by contacting a vaporized feed hydrocarbon with a liquid phosphoric acid catalyst in a. reaction zone defined by a copper surface at a reaction temperature in the range from 280 to 690 F. and at a pressure from atmospheric to 7000 p. s. i. g., the feature of the present invention being maintaining a substantially static iilsn of phosphoric acid in contact with the metallic copper surface while forming a product and recovering the product.
  • a convertible hydrocarbon including an olefin such as polymerization of a mono-olefin having from 2 to 6 carbon atoms by contacting a vaporized feed hydrocarbon with a liquid phosphoric acid catalyst in a. reaction zone defined by a copper surface at a reaction temperature in the range from 280 to 690 F. and at a pressure
  • the substantially static film of liquid pho phoric acid may be maintained by providing a ferrous metal reactor which has its interior surface lined with a continuous metallic copper liner over which is provided a second liner of such as porous carbon brick.
  • the porous nature of the carbon brick allows phosphoric acid to filter therethrough onto the copper surface.
  • the phosphoric acid has substantially a slow flow rate through the carbon brick and causes a film oi phosphoric acid which is in a 1 substantially static condition to form on the copper liner.
  • the of phosphoric acid forms a protective film from. the dynamic flow of phosphoric acid past th carbon br ck in the interior of the reaction zone and protects the copper liner of same from the corrosive and erosive action or" the substantially high velocity flow of phosphoric acid.
  • a protective film of corrosion product may build up on the copper surface under the static film of phosphoric acid which serves to protect the copper liner from further corrosion, the substantially static film of phosphoric acid being maintained by the small amount of phosphoric acid filtering through the brick liner.
  • the temperatures employed in the practice of the present invention may range from 280 to about 600 F.
  • a preferred temperature range is from 300 to 500 F.
  • Pressures employed in the practice of the present invention may range from atmospheric up to about 7000 p. s. i. g., with a preferred range from about 309 to 500 p. s. i. g. Increasing the pressure results in increased contact times and increases the yields to a remarkable extent.
  • the olefin containing feed stock may be employed in either the liquid or the vapor phase and it may contact the liquid phosphoric acid concurrently in the reaction zone defined by the metallic copper surface in accordance with the present invention.
  • Another way of contacting the liquid phosphoric acid catalyst with the olefin-containing feed is by forming a pool or column of the liquid phosphoric acid catalyst and allowing the olefin feed to bubble upwardly therethrough through suitable jets. It is desirable in the practice of the present invention to provide contacting material, such as carbon Berl saddles, Raschig rings, other packing, and any of the conventional distribution means employed. Glass and other silica-containing materials are attacked readily by the strong phosphoric acids at reaction conditions and. are, therefore, undesirable as packing materials.
  • Substantially pure silica such as fused silica or pure silica sand is not substantially attacked and may be employed.
  • materials such as nickel-nolybdenum-iron alloys, tantalum, illiurn, and the like which are not attacked by phosphoric acid and which might suitable packing material, but these are generally too expensive to be employed in com ercial operations.
  • the olefin feed the oleiins in a vaporize condition may be introduced preferably under concurrent flow conditions.
  • the preheated vaporized olefinic feed and phosphoric acid are introduced into the top of the reactor whose interior surface is defined by a metallic copper liner and the liquid catalyst flows down over the packing and out of the bottom of the reactor through an outlet into a separator from which it is pumped back to the reactor inlet. Any hydrocarbon phase that may be condensed in the reactor near the reactor outlet also flows to the bottom of the reactor.
  • the combined streams flowing out of the bottom of the reactor are passed through a cooler and then the acid and hydrocarbon phases are discharged into a settler where the two phases are separated.
  • the hydrocarbon phase is then withdrawn from the separator and discharged into a suitable separating means, such as a distillation tower, to separate polymer and unreacted materials, which may be recycled, if desired, to the feed.
  • the olefins forming the feed of the present invention will include the olefins containing from two to about six carbon atoms in the molecule and may be exemplified by ethylene, propylene, the butylenes, pentylenes and hexylenes.
  • ethylene forms a portion of the feed stock it should be employed in admixture with another olefin having a greater number of carbon atoms since efforts to polymerize ethylene alone have been, largely unsuccessful in that low yields were obtained.
  • the olefin feed stock of the present invention may be used in the pure state or in admixture with other olefins or other hydrocarbons.
  • propylene is a preferred feed stock and it is usually obtained in the petroleum refinery in admixture with ethylene, propane, and possibly some butylenes and butadiene.
  • ethylene propane
  • butylenes and butadiene butylenes and butadiene.
  • a pure hydrocarbon will be the preferred feed stock, it is within the spirit and scope of my invention to use mixtures of the various olefins or mixtures of olefins with other hydrocarbons such as aromatics.
  • the liquid phosphoric acid is an aqueous acid which may vary in concentration from 50% to 115% HzPOi.
  • the acid concentrations most useful in the polymerization of olefins such as propylene, for example, are in the range from "15% to 115% of HsPOi.
  • numeral ll designates the wall of a ferrous metal pressure vessel it, such as a steel vessel.
  • the vessel i is provided with at least an inlet thereto and an outlet.
  • the vessel is has an inlet 12 for introduction of phosphoric acid into the reaction vessel and a second inlet i3 for introduction of olefinic feed.
  • the wall it is suitably provided with a copper liner i lwhich is arranged adjacent the wall ii of reaction vessel it. This copper liner may be provided as a continuous copper liner to protect the interior surface of the vessel l0.
  • a liner of carbon brick i5 which covers the copper liner It; thus as phosphoric acid is introduced into the vessel 60 through inlet 12 it contacts the carbon brick liner 95 which is of a porous nature and flows over packing material It in contact with the hydrocarbon feed.
  • the phosphoric acid slow- 1 filters through the carbon brick and comes into contact with the copper liner l4 and forms thereon a substantially static film of phosphoric acid which reacts with the copper to form corrosion products.
  • the substantially static film of phosphoric acid on the copper liner H the corrosion products are not swept off and the copper liner is protected from further corrosion by the phosphoric acid flowing through the reaction vessel II.
  • reaction products including phosphoric acid are withdrawn from the vessel [0 through outlet I! and may be discharged into cooling and separation zones for separation of the phosphoric acid and the hydrocarbons to allow recycling of the phosphoric acid and unreacted feed and recovery of the desired product.
  • the flow rate of the substantially static film of phosphoric acid on the copper liner I4 is essentially zero whereas the velocity of flow in the reactor vessel H) where the olefinic feed is contacted with the phosphoric acid may be as high as 1000 feet per minute.
  • the vessel 10 is substantially unattached by the corrosive nature of the phosphoric acid, the steel or ferrous metal vessel being protected by the copper liner I4 and the copper liner being protected by the static film of phosphoric acid maintained thereon by virtue of the porous carbon brick liner [5 arranged in juxtaposition with the copper liner.
  • the corrosive rate of 98% H3PO4 to copper at a temperature of 360 F. increases from 0.015 to 0.05 inch per year when the rate of phosphoric acid flow over a copper surface is increased from substantially 0 to 4 feet per minute.
  • phosphoric acid is substantially noncorrosive to copper but under dynamic flow conditions it is very corrosive to a copper surface.
  • the present invention is adapted broadly to conversion operations, such as alkylation and polymerization in which an olefinic feed is employed.
  • the invention may be used in polymerizing mono-olefins to olefins having higher molecular weights than the olefinic feed.
  • the present invention may also be employed in the alkylation of aromatics with olefins.
  • an excess of an alkylatable aromatic hydrocarbon such as benzene, toluene, xylene, or the like
  • an olefin in the presence of liquid phosphoric acid under suitable conditions of temperature and pressure as mentioned before with respect to polymerization, to form an alkylated aromatic hydrocarbon
  • the olefins employed as alkylating agents will include the olefins enumerated before, as well as olefins of higher molecular weight, such for instance, as those having nine to twelve carbon atoms.
  • the invention may be employed in other catalytic operations where phosphoric acid catalysts of the type illustrated are used.
  • Illustrative of such operations including the contacting of liquid phosphoric acid with hydrocarbons or their derivatives at an elevated temperature, are the alkylation of phenols, and the like, with olefins.
  • Apparatus for converting hydrocarbons by contact with a liquid phosphoric acid catalyst which comprises a ferrous metal vessel having at least an inlet and an outlet, a continuous copper liner in said vessel arranged adjacent and directly contacting an interior surface of said vessel, and a carbon liner arranged adjacent and directly contacting the copper liner to cover said copper liner, said carbon liner being of a substantially porous material to allow flow of phosphoric acid therethrough.
  • a ferrous metal vessel having at least an inlet and an outlet, a continuous metallic copper liner arranged in said vessel in juxtaposition with and directly contacting an interior surface thereof, a carbon brick liner arranged in said vessel in juxtaposition with and directly contacting said copper liner to cover same and to form a lining of carbon brick in said vessel and a body of substantially inert packing material arranged in said vessel adapted to provide a contacting surface for hydrocarbons and phosphoric acid.

Description

Nov. 24, 1953 S. R. BETHEA APPARATUS FOR CATALYTIC CONVERSION OF HYDROCARBONS Original Filed May 28, 1951 Olefin Feed- Packing\ Carbon Brick m v/Awr Copper Liner\ I 1mm -1/ -Phosphoric Acid INVENTOR.
Sam R. Befhea,
iatenteol Nov. 24, 1953 Sam R. Bethea, Baytown, Tex, assignor, by mesne assignments,
Delaware to Standard Oil Development Company, Elizabeth, N.
5., a corporation of Original application May 28, 1951, Serial No.
1952, Serial No. 289,132
(Cl. 23-2S8) .2 Claims.
The present invention is directed to a method and apparatus for converting hydrocarbons. More particularly, the invention is directed to the catalytic conversion of a convertible hydrocarbon feed including an olefin. The invention is specifically directed to polymerization of olefins.
This application is a division of Serial No. 228,594 entitled Catalytic Conversion Method Apparatus Thereior filed May 28, 1951, in the name of Sam P... Bethea.
The present invention may be described brieily as involving the catalytic conversion of a convertible hydrocarbon including an olefin such as polymerization of a mono-olefin having from 2 to 6 carbon atoms by contacting a vaporized feed hydrocarbon with a liquid phosphoric acid catalyst in a. reaction zone defined by a copper surface at a reaction temperature in the range from 280 to 690 F. and at a pressure from atmospheric to 7000 p. s. i. g., the feature of the present invention being maintaining a substantially static iilsn of phosphoric acid in contact with the metallic copper surface while forming a product and recovering the product.
The substantially static film of liquid pho phoric acid may be maintained by providing a ferrous metal reactor which has its interior surface lined with a continuous metallic copper liner over which is provided a second liner of such as porous carbon brick. The porous nature of the carbon brick allows phosphoric acid to filter therethrough onto the copper surface. The phosphoric acid has substantially a slow flow rate through the carbon brick and causes a film oi phosphoric acid which is in a 1 substantially static condition to form on the copper liner. The of phosphoric acid forms a protective film from. the dynamic flow of phosphoric acid past th carbon br ck in the interior of the reaction zone and protects the copper liner of same from the corrosive and erosive action or" the substantially high velocity flow of phosphoric acid. It is believed that a protective film of corrosion product may build up on the copper surface under the static film of phosphoric acid which serves to protect the copper liner from further corrosion, the substantially static film of phosphoric acid being maintained by the small amount of phosphoric acid filtering through the brick liner.
The temperatures employed in the practice of the present invention may range from 280 to about 600 F. A preferred temperature range is from 300 to 500 F.
Divided and this application May 21,
Pressures employed in the practice of the present invention may range from atmospheric up to about 7000 p. s. i. g., with a preferred range from about 309 to 500 p. s. i. g. Increasing the pressure results in increased contact times and increases the yields to a remarkable extent.
In practicing the present invention the olefin containing feed stock may be employed in either the liquid or the vapor phase and it may contact the liquid phosphoric acid concurrently in the reaction zone defined by the metallic copper surface in accordance with the present invention. Another way of contacting the liquid phosphoric acid catalyst with the olefin-containing feed is by forming a pool or column of the liquid phosphoric acid catalyst and allowing the olefin feed to bubble upwardly therethrough through suitable jets. It is desirable in the practice of the present invention to provide contacting material, such as carbon Berl saddles, Raschig rings, other packing, and any of the conventional distribution means employed. Glass and other silica-containing materials are attacked readily by the strong phosphoric acids at reaction conditions and. are, therefore, undesirable as packing materials. Substantially pure silica, such as fused silica or pure silica sand is not substantially attacked and may be employed. There are other materials, such as nickel-nolybdenum-iron alloys, tantalum, illiurn, and the like which are not attacked by phosphoric acid and which might suitable packing material, but these are generally too expensive to be employed in com ercial operations.
In an operation Where packing materials are employed for contacting the phosphoric aci" with. the olefin feed the oleiins in a vaporize condition may be introduced preferably under concurrent flow conditions. The preheated vaporized olefinic feed and phosphoric acid are introduced into the top of the reactor whose interior surface is defined by a metallic copper liner and the liquid catalyst flows down over the packing and out of the bottom of the reactor through an outlet into a separator from which it is pumped back to the reactor inlet. Any hydrocarbon phase that may be condensed in the reactor near the reactor outlet also flows to the bottom of the reactor. The combined streams flowing out of the bottom of the reactor are passed through a cooler and then the acid and hydrocarbon phases are discharged into a settler where the two phases are separated. The hydrocarbon phase is then withdrawn from the separator and discharged into a suitable separating means, such as a distillation tower, to separate polymer and unreacted materials, which may be recycled, if desired, to the feed.
The olefins forming the feed of the present invention will include the olefins containing from two to about six carbon atoms in the molecule and may be exemplified by ethylene, propylene, the butylenes, pentylenes and hexylenes. When ethylene forms a portion of the feed stock it should be employed in admixture with another olefin having a greater number of carbon atoms since efforts to polymerize ethylene alone have been, largely unsuccessful in that low yields were obtained. It is contemplated that the olefin feed stock of the present invention may be used in the pure state or in admixture with other olefins or other hydrocarbons. For example, propylene is a preferred feed stock and it is usually obtained in the petroleum refinery in admixture with ethylene, propane, and possibly some butylenes and butadiene. Thus, while a pure hydrocarbon will be the preferred feed stock, it is within the spirit and scope of my invention to use mixtures of the various olefins or mixtures of olefins with other hydrocarbons such as aromatics.
In the practice of my invention, the liquid phosphoric acid is an aqueous acid which may vary in concentration from 50% to 115% HzPOi. The acid concentrations most useful in the polymerization of olefins such as propylene, for example, are in the range from "15% to 115% of HsPOi.
In the practice of my invention, it is also desirable to exclude free oxygen from the materials whiciv come in contact with the copper reactor lining. This is, in general, satisfactorily achieved by excluding oxygen from the hydrocarbon feed by well-known means, such as by blanketing the feed hydrocarbon storage tanks with an inert or by adding an oxidation inhibitor of t e phenolic or quinoid type, such as para-tort. butyl catechol or hydroquinone to the hydrocarbon in small but effective amounts of no more than 1 per cent or by treating the free oxygcn-containing hydrocarbon solution with an oxygen-consuming reagent such as an alkaline solution of pyrogallol or of cuprous oxide. Oxygen may also be removed from the hydrocarbon by a stripping or distillation operation.
The invention will be further illustrated by reference to the drawing in which the sole figure a sectional view of a reaction vessel illustrating the how of reactants and catalyst as well as the liners therefor.
Reierri. now to the drawing, numeral ll designates the wall of a ferrous metal pressure vessel it, such as a steel vessel. The vessel i is provided with at least an inlet thereto and an outlet. The vessel is has an inlet 12 for introduction of phosphoric acid into the reaction vessel and a second inlet i3 for introduction of olefinic feed. The wall it is suitably provided with a copper liner i lwhich is arranged adjacent the wall ii of reaction vessel it. This copper liner may be provided as a continuous copper liner to protect the interior surface of the vessel l0. Superimposed on the copper liner I4 is a liner of carbon brick i5 which covers the copper liner It; thus as phosphoric acid is introduced into the vessel 60 through inlet 12 it contacts the carbon brick liner 95 which is of a porous nature and flows over packing material It in contact with the hydrocarbon feed. The phosphoric acid slow- 1: filters through the carbon brick and comes into contact with the copper liner l4 and forms thereon a substantially static film of phosphoric acid which reacts with the copper to form corrosion products. By virtue of the substantially static film of phosphoric acid on the copper liner H, the corrosion products are not swept off and the copper liner is protected from further corrosion by the phosphoric acid flowing through the reaction vessel II. The reaction products including phosphoric acid are withdrawn from the vessel [0 through outlet I! and may be discharged into cooling and separation zones for separation of the phosphoric acid and the hydrocarbons to allow recycling of the phosphoric acid and unreacted feed and recovery of the desired product.
The flow rate of the substantially static film of phosphoric acid on the copper liner I4 is essentially zero whereas the velocity of flow in the reactor vessel H) where the olefinic feed is contacted with the phosphoric acid may be as high as 1000 feet per minute.
Thus, in accordance with the present invention, it is possible to provide a method and apparatus therefor for converting hydrocarbons whereby the vessel 10 is substantially unattached by the corrosive nature of the phosphoric acid, the steel or ferrous metal vessel being protected by the copper liner I4 and the copper liner being protected by the static film of phosphoric acid maintained thereon by virtue of the porous carbon brick liner [5 arranged in juxtaposition with the copper liner.
To illustrate the beneficial effects of the present invention, it has been found that the corrosive rate of 98% H3PO4 to copper at a temperature of 360 F. increases from 0.015 to 0.05 inch per year when the rate of phosphoric acid flow over a copper surface is increased from substantially 0 to 4 feet per minute. In other words, under static conditions phosphoric acid is substantially noncorrosive to copper but under dynamic flow conditions it is very corrosive to a copper surface. By providing a reaction vessel with a copper liner wherein a static film of phosphoric acid is maintained on the liner, it is possible to conduct con version operations such as polymerization and alkyiation without destruction of the vessel.
The present invention is adapted broadly to conversion operations, such as alkylation and polymerization in which an olefinic feed is employed. For example the invention may be used in polymerizing mono-olefins to olefins having higher molecular weights than the olefinic feed.
The present invention may also be employed in the alkylation of aromatics with olefins. In such reactions, an excess of an alkylatable aromatic hydrocarbon, such as benzene, toluene, xylene, or the like, is contacted with an olefin in the presence of liquid phosphoric acid under suitable conditions of temperature and pressure as mentioned before with respect to polymerization, to form an alkylated aromatic hydrocarbon The olefins employed as alkylating agents will include the olefins enumerated before, as well as olefins of higher molecular weight, such for instance, as those having nine to twelve carbon atoms.
The invention may be employed in other catalytic operations where phosphoric acid catalysts of the type illustrated are used. Illustrative of such operations including the contacting of liquid phosphoric acid with hydrocarbons or their derivatives at an elevated temperature, are the alkylation of phenols, and the like, with olefins.
While the invention has been described and illustrated by reference to a reaction zone defined by a metallic copper surface in which the film of phosphoric acid is maintained thereon by providing a liner of porous carbon brick superimposed on the copper liner, it is understood that the invention may be practiced with other apparatus wherein a static film of phosphoric acid is maintained on the copper liner. For example, it may be desirable to provide a copper lined reactor having a baflle of material which is un susceptible to attack by phosphoric acid to protect the copper liner from dynamic flow of phosphoric acid. The copper liner may then be flooded with phosphoric acid to provide a film thereon and the excess phosphoric acid drained from the surface of the copper. It may be necessary when such operations are conducted to renew the film of phosphoric acid periodically.
The nature and objects of the present invention having been completely described and illustrated, what I Wish to claim as new and useful and to secure by Letters Patent is:
1. Apparatus for converting hydrocarbons by contact with a liquid phosphoric acid catalyst, which comprises a ferrous metal vessel having at least an inlet and an outlet, a continuous copper liner in said vessel arranged adjacent and directly contacting an interior surface of said vessel, and a carbon liner arranged adjacent and directly contacting the copper liner to cover said copper liner, said carbon liner being of a substantially porous material to allow flow of phosphoric acid therethrough.
2. Apparatus for converting hydrocarbons by contact with a liquid phosphoric acid catalyst,
which comprises a ferrous metal vessel having at least an inlet and an outlet, a continuous metallic copper liner arranged in said vessel in juxtaposition with and directly contacting an interior surface thereof, a carbon brick liner arranged in said vessel in juxtaposition with and directly contacting said copper liner to cover same and to form a lining of carbon brick in said vessel and a body of substantially inert packing material arranged in said vessel adapted to provide a contacting surface for hydrocarbons and phosphoric acid.
SAM R. BE'IHEA.
References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 2,354,163 Weizmann et al. July 18, 1944 2,374,511 Upham Apr. 24, 1945 2,415,797 LOW Feb. 11, 1947 OTHER REFERENCES Chem. Ind., pages 683-688, May 1944.

Claims (1)

1. APPARATUS FOR CONVERGING HYDROCARBONS BY CONTACT WITH A LIQUID PHOSPHORIC ACID CATALYST, WHICH COMPRISES A FERROUS METAL VESSEL HAVING AT LEAST AN INLET AND AN OUTLET, A CONTINUOUS COPPER LINER IN SAID VESSEL ARRANGED ADJACENT AND DIRECTLY CONTACTING AN INTERIOR SURFACE OF SAID VESSEL, AND A CARBON LINER ARRANGED ADJACENT AND DIRECTLY CONTACTING THE COPPER LINER TO COVER SAID COPPER LINER, SAID CARBON LINER BEING OF A SUBSTANTIALLY POROUS MATERIAL TO ALLOW FLOW OF PHOSPHORIC ACID THERETHROUGH.
US289132A 1951-05-28 1952-05-21 Apparatus for catalytic conversion of hydrocarbons Expired - Lifetime US2660520A (en)

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US289132A US2660520A (en) 1951-05-28 1952-05-21 Apparatus for catalytic conversion of hydrocarbons

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US228594A US2702827A (en) 1951-05-28 1951-05-28 Reduction of phosphoric acid corrosion in. a polymerization process
US289132A US2660520A (en) 1951-05-28 1952-05-21 Apparatus for catalytic conversion of hydrocarbons

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3017255A (en) * 1959-07-02 1962-01-16 Norris William Arthur Oxidizer
US3155742A (en) * 1961-09-11 1964-11-03 Shell Oil Co Alkylation process
US3235344A (en) * 1963-02-18 1966-02-15 Chevron Res Hydrocarbon conversion catalytic reactor

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2354163A (en) * 1941-08-06 1944-07-18 Weizmann Charles Lining for hydrocarbon treating apparatus
US2374511A (en) * 1943-04-09 1945-04-24 Phillips Petroleum Co Process for effecting catalytic reactions
US2415797A (en) * 1942-10-02 1947-02-11 Westvaco Chlorine Products Cor Preparation of pure phosphoric acid

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2354163A (en) * 1941-08-06 1944-07-18 Weizmann Charles Lining for hydrocarbon treating apparatus
US2415797A (en) * 1942-10-02 1947-02-11 Westvaco Chlorine Products Cor Preparation of pure phosphoric acid
US2374511A (en) * 1943-04-09 1945-04-24 Phillips Petroleum Co Process for effecting catalytic reactions

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3017255A (en) * 1959-07-02 1962-01-16 Norris William Arthur Oxidizer
US3155742A (en) * 1961-09-11 1964-11-03 Shell Oil Co Alkylation process
US3235344A (en) * 1963-02-18 1966-02-15 Chevron Res Hydrocarbon conversion catalytic reactor

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