US2173984A - Apparatus and process for catalytic reactions - Google Patents

Apparatus and process for catalytic reactions Download PDF

Info

Publication number
US2173984A
US2173984A US161715A US16171537A US2173984A US 2173984 A US2173984 A US 2173984A US 161715 A US161715 A US 161715A US 16171537 A US16171537 A US 16171537A US 2173984 A US2173984 A US 2173984A
Authority
US
United States
Prior art keywords
tubes
furnace
catalyst
tube
gas
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US161715A
Inventor
James H Shapleigh
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hercules Powder Co
Original Assignee
Hercules Powder Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to BE429915D priority Critical patent/BE429915A/xx
Priority to US21521D priority patent/USRE21521E/en
Application filed by Hercules Powder Co filed Critical Hercules Powder Co
Priority to US161715A priority patent/US2173984A/en
Priority to DEH3052D priority patent/DE887801C/en
Application granted granted Critical
Publication of US2173984A publication Critical patent/US2173984A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • 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
    • B01J8/06Chemical 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 in tube reactors; the solid particles being arranged in tubes
    • B01J8/062Chemical 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 in tube reactors; the solid particles being arranged in tubes being installed in a furnace
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/34Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
    • C01B3/38Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts
    • C01B3/384Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts the catalyst being continuously externally heated

Definitions

  • 'Ihis invention relates to improved apparatus and process for catalytic reactions involving the application of heat to gases and vapors, particularly adapted to the art of producing gas rich in 5' free hydrogen from hydrocarbon gas with steam or other compounds containing oxygen, which may react with the carbon of the hydrocarbons.
  • Another special method heretofore in use has 40 been the use of high proportions of excess air in the combustion gases, in order to reduce the temi perature of the gases to a suitable point.
  • the exit temperatures are all below the melting point of the alloy tube.
  • the thermal eihciency is then about 2li-35%, a very low value.
  • the temperature differential for heating the hot end of the tube and furnace wall is low, 500 F. maximum at 28% thermal elciency.
  • the construction and design of such old apparatus necessitates a substantial temperature difference (250 F.500 F.) between the furnace wall and the metal tube, making high operating temperature diiiicult to obtain. It is therefore evident that the old apparatus design, including provision for parallel flow, represents a common and specific state in the artV and one not meeting thedemand for cheap hydrogen.
  • I may use counter-ciment flow with the combustion gases containing a minimum of excess air, and by the use of high temperature combustion gases, without endangering the metal alloy catalyst tubes. Such I accomplish by the use of a heating furnace containing the catalyst tubes hereinafter more fully described.
  • My improved apparatus enables not only higher thermal efficiency to be obtained, but higher chemical eficiency. This is due to the fact that the tube wall temperature can be very close to the refractory wall temperature, and for any specified thermal efficiency for the furnace, as compared to a parallel flow operated furnace, the tube operating temperatures will be higher, which gives directly higher chemical efliciency.
  • I represents a furnace. constructed preferably of fire: brick, containing metal alloy catalyst tubes 2, placed vertically in planes parallel to the side walls of the furnace. Any number of such tubes may be used, arranged, for example, as is more fully described in connection with Figure 2.
  • the tubes are constructed of a nickel-chromium-iron alloy adapted to withstand high temperatures.
  • the tubes 2 project through the top and bottom of the furnace, passing through tiles 3.
  • the projecting ends of the tubes and the outer surface of the furnace may, if desired, be covered with insulating material (not shown to enhance clarity).
  • Tubes 2 are supported by means of any suitable support at the top of each tube, e.
  • the upper flange 5 of tube 2 rests upon a short collar 6, through which tube 2 may pass freely.
  • Collar 6 is supported by and fastened to steel beam l, supported in any suitable manner upon the furnace housing. Any of tubes 2 may be readily removed from the furnace by disconnecting it at the :flange and lifting it vertically from the furnace.
  • Tubes 2 are filled with a suitable catalytic material 8, supported by a perforated alloy plate 9. Suitable catalysts are hereinafter disclosed. Plate 9 is removable, and rests upon support I0, attached to the inner surface of the tube.
  • the tubes 2 may be removed and replaced, even when filled with catalyst, in the manner already described, and the catalyst may be placed in the tubes, or removed therefrom, both while the tubes are in the furnace or at other places remote from.
  • gases or vapors are supplied through convenient pipes, which may differ from those shown in the accompanying drawings as circumstances and process may require.
  • a mixture of hydrocarbon gas and steam is forced through line II, controlled by valve I2, into tubes 2.
  • Burners I5 are located in the side wall of furnace I at various levels. Suitable burners are those giving a short flame, such as inspirator type N571-A, made by the Surface Combustion Corporation. Gas is supplied to the burners through gas pipes I6, the pressure being indicated by gauge I'I. The combustion gases from the burners pass into the furnace substantially tangentlally to tubes 2. and pas: upward around the tubes with a circulatory motion, at the same time heating the inner furnace walls to a high temperature and radiating heat from said walls to tubes 2. The gases of combustion finally escape from the furnace in a flue Il, connecting with a stack (not shown). Suitable heat exchange equipment or waste heat boilers'may be used to recover heat remaining in said flue gas.
  • a mixture of steam and hydrocarbon gas is passed down through pipes 2 and through catalyst mass 8, where it is heated rapidly to a temperature of about 1600 to about 2000" F.
  • a temperature of about 1600 to about 2000" F At such temperatures there' is a marked decrease in the strength of alloys used for the catalyst tubes, and serious bending and distortion occur if said tubes are supported at the bottom. Suspension of the tubes at the top, leaving the bottom and connections thereto free to move with thermal expansion of the tube, prevents this distortion.
  • each chamber of which contains catalyst tubes having the herein defined relation of tube surface to vertical wail surface, preferably about 3 inches to about 8 inches in diameter, but not exceeding 12 inches in diameter, and preferably about 25 feet long, but not exceeding 50 feet4 in length.
  • Suitable catalysts for the production of hydrogen by cracking hydrocarbon gases possess high activity and physical strength, and shrink very little at the operating temperatures employed.
  • Calcium and magnesium oxides and silica may be added to produce catalysts of greater strength at high temperatures.
  • Phosphoric acid with alumina and nickel oxide produce a very active catalyst, which shrinks very little at high tempera tures.
  • a particularly suitable catalyst is prepared from nickel oxides, magnesia and kaolin. The catalyst is usually prepared in the form of a paste, cut into small cubes, dried slowly, then heated slowly in the presence of steam to a temperature of about 500 F.
  • my catalyst in my furnace comprising diaspore impregnated with nickel nitrate so as to contain about 6% by weight of nickel, and heating to about 500 F. to decompose the nitrate, then reduced by passing therethrough hot reducing gases.
  • my catalyst mass comprises particles from about to about in diameter.
  • the gas may be cooled immediately after leaving the furnace, if a hydrogen-carbon monoxide mixture is desired for the production of synthetic alcohol, or, if a. gas containing almost entirely hydrogen is desired, it is preferable to pass the exist gas, with added steam over iron oxides or other suitable catalyst in the known manner, for conversion of carbon monoxide to carbon dioxide, then cool the gas, scrub out the carbon dioxide by known means, leaving a hydrogen oi about 95% purity.
  • My appl'atus may be Operated at any desired pressure above or below atmospheric, limited only by strength of materials at the operating temperature employed.
  • a process for preparing hydrogen which comprises passing reactants comprising gaseous hydrocarbons and steam downwardly through elongate ⁇ vertical tubes contained in a heating zone, simultaneously heating said reactants indirectly by introducing hot flaming gases into said heating zone at a plurality of vertically spaced points along and adjacent to said tubes and substantially tangentially to saidtubes, and withdrawing the resulting combustion gases at a. point adjacent the top oi' said zone, whereby said flaming gases follow an upwardly ascending rotary path around said tubes, Vwhich are thereby uniformly heated without substantial flame impingement thereon.
  • a process for preparing hydrogen which comprises passing reactants comprising gaseous hydrocarbons and steam downwardly through elongate vertical catalyst tubes contained in a heating zone, heating said ,reactants indirectly by introducing hot combustion gases into said heating zone at a plurality of vertically spaced points along and adjacent to said tubes and substantially tangentially to said tubes, withdrawing the treated reactants from adjacent the bottom of the said tubes and withdrawing the combustion gases at a point adjacent the top of said heating zone, whereby said hot combustion gases follow an upwardly ascending rotary path around said tubes, which are thereby uniformly heated without substantial flame impingement thereon.
  • a process for preparing hydrogen which comprises passing reactants comprising gaseous hydrocarbons and steam downwardly through a bank oi' substantially vertically disposed catalyst tubes contained in a heating zone, heating said 'flame impingement thereon.
  • a process for preparing hydrogen which comprises passing reactants comprising gaseous hydrocarbons and steam downwardly through a bank of substantially vertically disposed catalyst tubes contained in a refractorywalled heating zone, maintaining a ratio of from 1 to 10 square feet of refractory wall surface to each square foot of catalyst tube surface, heating said reactants indirectlyby introducing hot combustion gases into said heating zone substantially tangentially to said bank of tubes and at a plurality of vertically spaced points along and adjacent to said bank, withdrawing the treated reactants from adjacent the bottom of the tubes and withdrawing combustion gases at a point adjacent the top of said heating zone, whereby said hot combustion gases follow an upwardly ascending rotary lpath around said bank of tubes, which is thereby uniformly heated without substantial flame impingement thereon.
  • a process for preparing hydrogen which comprises passing reactants comprising gaseous hydrocarbons and steam downwardly through a bank of substantially vertically disposed catalyst tubes contained in a refractory-walled heating zone, maintaining a ratio of from 2 to 6 square feet of refractory wall surface to each square foot of catalyst tube surface, heating said reactants indirectly by introducing hot combustion gases into said heating zone substantially ta'ngentially to said bank of tubes and at a plurality of vertically spaced points along and adjacent ,to said bank, withdrawing the treated reactants from adjacent the bottom of the tubes and withdrawing combustion gases at a point adjacent the top of said heating zone, whereby said hot combustion gases follow an upwardly ascending rotary path around said bank of tubes, which is thereby uniformly heated without substantial flame impingement thereon.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Inorganic Chemistry (AREA)
  • Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
  • Physical Or Chemical Processes And Apparatus (AREA)

Description

Sept. 26, 1939. '.1. H. SHAPLEIGH APPARATUS AND PROCESS FOR CATALYTIC REACTIONS Filed Augfo, 1957 2 Sheets-Sheet 1 :l f l 0 ///////0/////////// "JAMES H SHAPLEIGH FlG.l
.lNvENToR BY GMM ATTORNEY Sept 26, 1939 J. H. sHAFuJ-:IGI-a 2,173,984
APPARATUS AND PROCESS FOR CATALYTIOREACTIONS Filed Aug. 30, 1937 2l Sheets-Sheet 2 FIG.2
JAM ES HSHAPLEIGH INVENTOR ATTORNEY Patented Sept. 26, 1939 OFFICE .APPARATUS AND PROCESS FOR CATALYTIC REACTIONS James H.
Claims.
'Ihis invention relates to improved apparatus and process for catalytic reactions involving the application of heat to gases and vapors, particularly adapted to the art of producing gas rich in 5' free hydrogen from hydrocarbon gas with steam or other compounds containing oxygen, which may react with the carbon of the hydrocarbons.
In reacting hydrocarbon gases with steam to produce hydrogen, it is desirable to use high temperatures, e. g., up to 2000 F. Although special metal tubes, filled with catalyst, are known to the art. the economical use of such tubes and catalyst has not yet been disclosed. To prevent tubes heated to temperatures of l600-2000 F. from failing, special methods have heretofore been used, due to the fact that combustion temperature in the heating furnace may be of the order of 3500 F., a temperature higher than the melting point of the alloy steel tubes used.
One of the special methods of heating heretofore known is to Aapply parallel flow, whereby combustion gases of the highest temperature contact the coolest portion of the reaction tube. Such a method sends'gases from the furnace at its base at a very high temperature, since the lower end of the tubes may be as high as 2000 F., and with an endothermic reaction it is obviously necessary to have the supply of heat such that a vtemperature gradient can be maintained. An
additional protective measure sometimes used by the prior art, even with the use of parallel ow, has been the spacing of the reaction tubes at substantial distances one from the other so as to provide considerable room for the combustion gases within the furnace. An example of such spacing is to have the distance from tube center to tube center equal to approximately nine tube diameters.
Another special method heretofore in use has 40 been the use of high proportions of excess air in the combustion gases, in order to reduce the temi perature of the gases to a suitable point.
All of the above special methods are uneconomical in use, in that they tend to low thermal 5f etlciency and require, for economy, recovery of excess or Waste heat or the use of waste heat boilers or the like.
In all of the above cases, where parallel flow exists between process gas within the tube and hot combustion gas without, the objective has been to obtain safe mechanical and physical conditions. For example, a combustion gas of a temperature of about 3500 F., passing parallel to a. tube with maximum end temperature of about Il 2000 F., mustleave the apparatus -at a tempera- Shapleigh, Wilmington, to Hercules Powder Company, a corporation oi' Delaware Appiition August 30,1937, serial No. 161,715
Del., assigner Wilmington, Del.,
REISSUED JUL? o 1940 ture higher than 2ooo F., say 2250 Under this condition,
F. to 2500 F.
the exit temperatures are all below the melting point of the alloy tube. The thermal eihciency is then about 2li-35%, a very low value. In addition. the temperature differential for heating the hot end of the tube and furnace wall is low, 500 F. maximum at 28% thermal elciency. The construction and design of such old apparatus necessitates a substantial temperature difference (250 F.500 F.) between the furnace wall and the metal tube, making high operating temperature diiiicult to obtain. It is therefore evident that the old apparatus design, including provision for parallel flow, represents a common and specific state in the artV and one not meeting thedemand for cheap hydrogen.
I have found that I may use counter-ciment flow with the combustion gases containing a minimum of excess air, and by the use of high temperature combustion gases, without endangering the metal alloy catalyst tubes. Such I accomplish by the use of a heating furnace containing the catalyst tubes hereinafter more fully described.
When starting with the same gas at 3500 F. I obtain an exit gas of approximately 1300* F., or an eiilciency of about 63%, in marked contrast to the 28-35% obtained by parallel ow. My use of from 1 to 10 square 'feet of parallel refractory Wall surface radiating to each square foot of metal tube surface Within the furnace, say 2 to 6, I find enables me to utilize small diierences between metal tube and refractory wall temperature at the hottest point of the tube. This temperature difference may be 50 F. or less, depending upon the relationship used. This is'in contrast to 250 to 500 F. by the disclosed art. Further, I nd I can use a high differential (1000 to 1500 F.) between combustion gas and refractory wall at the process gas exit end of the apparatus, without any detrimental effect on the metal tube, even though its melting point is substantially below the combustion gas temperature.
Also, in my furnace I use counteriiow heating, with a defined relationship between combusion gas and metal tube surface, e. g., when using a natural gas containing approximately methane and 20% ethane, I prefer to use, per lineal foot of furnace height, about 10 to about cubic .feet of gas per hour per square foot of metal tube wall contained within that unit foot of vertical height, with spatial velocity of cracking gas about 600 cubic feet per hour per cubic foot of catalyst. I contemplate the use of suitable 55 burners, hereinafter more fully exemplified, at a number of different levels for a multiple tube furnace, and I also contemplate passing burner gases initially substantially tangentially to the tubes, the gases thus producing a circulatory motion as they pass counter-current to the tubes.
My improved apparatus enables not only higher thermal efficiency to be obtained, but higher chemical eficiency. This is due to the fact that the tube wall temperature can be very close to the refractory wall temperature, and for any specified thermal efficiency for the furnace, as compared to a parallel flow operated furnace, the tube operating temperatures will be higher, which gives directly higher chemical efliciency.
My invention will be more fully understood by reference to the accompanying drawings, which illustrate one form of apparatus suitable for my invention. The drawings are, Figure 1, an elevation, and Figure 2, a plan of apparatus constructed according to the present invention.
Referring now particularly to Figure 1 of the accompanying drawings, I represents a furnace. constructed preferably of fire: brick, containing metal alloy catalyst tubes 2, placed vertically in planes parallel to the side walls of the furnace. Any number of such tubes may be used, arranged, for example, as is more fully described in connection with Figure 2. The tubes are constructed of a nickel-chromium-iron alloy adapted to withstand high temperatures. The tubes 2 project through the top and bottom of the furnace, passing through tiles 3. The projecting ends of the tubes and the outer surface of the furnace may, if desired, be covered with insulating material (not shown to enhance clarity). Tubes 2 are supported by means of any suitable support at the top of each tube, e. g., the upper flange 5 of tube 2 rests upon a short collar 6, through which tube 2 may pass freely. Collar 6 is supported by and fastened to steel beam l, supported in any suitable manner upon the furnace housing. Any of tubes 2 may be readily removed from the furnace by disconnecting it at the :flange and lifting it vertically from the furnace.
Tubes 2 are filled with a suitable catalytic material 8, supported by a perforated alloy plate 9. Suitable catalysts are hereinafter disclosed. Plate 9 is removable, and rests upon support I0, attached to the inner surface of the tube. The tubes 2 may be removed and replaced, even when filled with catalyst, in the manner already described, and the catalyst may be placed in the tubes, or removed therefrom, both while the tubes are in the furnace or at other places remote from.
the furnace.
The gases or vapors are supplied through convenient pipes, which may differ from those shown in the accompanying drawings as circumstances and process may require. In the present example, a mixture of hydrocarbon gas and steam is forced through line II, controlled by valve I2, into tubes 2.
The gases leaving the bottom of tubes 2 pass through separate lines I3 into headers I4, suitably supported (not shown) and free to move with expansion and contraction of tubes 2.
Burners I5, not all shown in detail, are located in the side wall of furnace I at various levels. Suitable burners are those giving a short flame, such as inspirator type N571-A, made by the Surface Combustion Corporation. Gas is supplied to the burners through gas pipes I6, the pressure being indicated by gauge I'I. The combustion gases from the burners pass into the furnace substantially tangentlally to tubes 2. and pas: upward around the tubes with a circulatory motion, at the same time heating the inner furnace walls to a high temperature and radiating heat from said walls to tubes 2. The gases of combustion finally escape from the furnace in a flue Il, connecting with a stack (not shown). Suitable heat exchange equipment or waste heat boilers'may be used to recover heat remaining in said flue gas.
In the present process, a mixture of steam and hydrocarbon gas is passed down through pipes 2 and through catalyst mass 8, where it is heated rapidly to a temperature of about 1600 to about 2000" F. At such temperatures there' is a marked decrease in the strength of alloys used for the catalyst tubes, and serious bending and distortion occur if said tubes are supported at the bottom. Suspension of the tubes at the top, leaving the bottom and connections thereto free to move with thermal expansion of the tube, prevents this distortion.
In the preferred embodiment of my invention, I employ a furnace, each chamber of which contains catalyst tubes having the herein defined relation of tube surface to vertical wail surface, preferably about 3 inches to about 8 inches in diameter, but not exceeding 12 inches in diameter, and preferably about 25 feet long, but not exceeding 50 feet4 in length. It will be observed that, in my improved furnace, the hydrocarbon gases flow counter to the combustion gases, and very high temperature combustion gases flow against a very hot tube, and, by means of burners placed at various'levels the temperature of the various zones is controlled as desired, at high velocity of combustion gases owing counter-current to the hydrocarbon gas.
Suitable catalysts for the production of hydrogen by cracking hydrocarbon gases possess high activity and physical strength, and shrink very little at the operating temperatures employed. Oxides or metals of the iron group, admixed with aluminum oxide, form desirable catalysts. Calcium and magnesium oxides and silica may be added to produce catalysts of greater strength at high temperatures. Phosphoric acid with alumina and nickel oxide produce a very active catalyst, which shrinks very little at high tempera tures. A particularly suitable catalyst is prepared from nickel oxides, magnesia and kaolin. The catalyst is usually prepared in the form of a paste, cut into small cubes, dried slowly, then heated slowly in the presence of steam to a temperature of about 500 F. higher than the operating temperature at which it is to be used, then held at this temperature for about 24-48 hours. Such roasting treatment causes most of the shrinkage to take place before use of thecatalyst. Dried catalyst may also be charged into the tubes, and the final roasting step then performed with the tubes in place in the furnace, additional catalyst being added to make up for shrinkage. The catalyst should not be roasted at so high a temperature as to cause serious decrease in catalytic activity.
I prefer to use a catalyst in my furnace comprising diaspore impregnated with nickel nitrate so as to contain about 6% by weight of nickel, and heating to about 500 F. to decompose the nitrate, then reduced by passing therethrough hot reducing gases. Preferably, my catalyst mass comprises particles from about to about in diameter.
The exist gas from the cracking of methane and steam consists almost entirely of hydrogen,
carbon oxides, and excess steam, usually containing a high percentage of carbon monoxide. The gas may be cooled immediately after leaving the furnace, if a hydrogen-carbon monoxide mixture is desired for the production of synthetic alcohol, or, if a. gas containing almost entirely hydrogen is desired, it is preferable to pass the exist gas, with added steam over iron oxides or other suitable catalyst in the known manner, for conversion of carbon monoxide to carbon dioxide, then cool the gas, scrub out the carbon dioxide by known means, leaving a hydrogen oi about 95% purity.
My appl'atus may be Operated at any desired pressure above or below atmospheric, limited only by strength of materials at the operating temperature employed. n Y
What I claim is:
1. A process for preparing hydrogen which comprises passing reactants comprising gaseous hydrocarbons and steam downwardly through elongate `vertical tubes contained in a heating zone, simultaneously heating said reactants indirectly by introducing hot flaming gases into said heating zone at a plurality of vertically spaced points along and adjacent to said tubes and substantially tangentially to saidtubes, and withdrawing the resulting combustion gases at a. point adjacent the top oi' said zone, whereby said flaming gases follow an upwardly ascending rotary path around said tubes, Vwhich are thereby uniformly heated without substantial flame impingement thereon.
2. A process for preparing hydrogen which comprises passing reactants comprising gaseous hydrocarbons and steam downwardly through elongate vertical catalyst tubes contained in a heating zone, heating said ,reactants indirectly by introducing hot combustion gases into said heating zone at a plurality of vertically spaced points along and adjacent to said tubes and substantially tangentially to said tubes, withdrawing the treated reactants from adjacent the bottom of the said tubes and withdrawing the combustion gases at a point adjacent the top of said heating zone, whereby said hot combustion gases follow an upwardly ascending rotary path around said tubes, which are thereby uniformly heated without substantial flame impingement thereon.
3. A process for preparing hydrogen which comprises passing reactants comprising gaseous hydrocarbons and steam downwardly through a bank oi' substantially vertically disposed catalyst tubes contained in a heating zone, heating said 'flame impingement thereon.
4. A process for preparing hydrogen which comprises passing reactants comprising gaseous hydrocarbons and steam downwardly through a bank of substantially vertically disposed catalyst tubes contained in a refractorywalled heating zone, maintaining a ratio of from 1 to 10 square feet of refractory wall surface to each square foot of catalyst tube surface, heating said reactants indirectlyby introducing hot combustion gases into said heating zone substantially tangentially to said bank of tubes and at a plurality of vertically spaced points along and adjacent to said bank, withdrawing the treated reactants from adjacent the bottom of the tubes and withdrawing combustion gases at a point adjacent the top of said heating zone, whereby said hot combustion gases follow an upwardly ascending rotary lpath around said bank of tubes, which is thereby uniformly heated without substantial flame impingement thereon.
5. A process for preparing hydrogen which comprises passing reactants comprising gaseous hydrocarbons and steam downwardly through a bank of substantially vertically disposed catalyst tubes contained in a refractory-walled heating zone, maintaining a ratio of from 2 to 6 square feet of refractory wall surface to each square foot of catalyst tube surface, heating said reactants indirectly by introducing hot combustion gases into said heating zone substantially ta'ngentially to said bank of tubes and at a plurality of vertically spaced points along and adjacent ,to said bank, withdrawing the treated reactants from adjacent the bottom of the tubes and withdrawing combustion gases at a point adjacent the top of said heating zone, whereby said hot combustion gases follow an upwardly ascending rotary path around said bank of tubes, which is thereby uniformly heated without substantial flame impingement thereon.
JAMES H. SHAPLEIGH.
US161715A 1937-08-30 1937-08-30 Apparatus and process for catalytic reactions Expired - Lifetime US2173984A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
BE429915D BE429915A (en) 1937-08-30
US21521D USRE21521E (en) 1937-08-30 Process for catalytic reaction
US161715A US2173984A (en) 1937-08-30 1937-08-30 Apparatus and process for catalytic reactions
DEH3052D DE887801C (en) 1937-08-30 1938-08-18 Contact furnace for the production of hydrogen-rich gases from gaseous hydrocarbons and water vapor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US161715A US2173984A (en) 1937-08-30 1937-08-30 Apparatus and process for catalytic reactions

Publications (1)

Publication Number Publication Date
US2173984A true US2173984A (en) 1939-09-26

Family

ID=22582393

Family Applications (2)

Application Number Title Priority Date Filing Date
US21521D Expired USRE21521E (en) 1937-08-30 Process for catalytic reaction
US161715A Expired - Lifetime US2173984A (en) 1937-08-30 1937-08-30 Apparatus and process for catalytic reactions

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US21521D Expired USRE21521E (en) 1937-08-30 Process for catalytic reaction

Country Status (3)

Country Link
US (2) US2173984A (en)
BE (1) BE429915A (en)
DE (1) DE887801C (en)

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2571953A (en) * 1947-09-19 1951-10-16 Hercules Powder Co Ltd Manufacture of hydrogen
US2638407A (en) * 1949-12-31 1953-05-12 Standard Oil Dev Co Apparatus for close temperature control of catalyzed gas reactions
US2645566A (en) * 1949-12-12 1953-07-14 Gas Machinery Co High-temperature reactor
US2660519A (en) * 1948-04-23 1953-11-24 Chemical Construction Corp Fluid heater
US2667410A (en) * 1950-01-04 1954-01-26 Phillips Petroleum Co Apparatus for reforming hydrocarbons
US2730434A (en) * 1950-05-01 1956-01-10 Oxy Catalyst Inc Catalytic contacting unit
US2743171A (en) * 1950-08-23 1956-04-24 United Gas Improvement Co Method for making gas rich in hydrogen
US2788266A (en) * 1951-10-13 1957-04-09 Stirnemann Ernst Catalytic reactor furnace
US2852358A (en) * 1954-06-10 1958-09-16 Commercial Solvents Corp Process for reforming hydrocarbons
US2860959A (en) * 1954-06-14 1958-11-18 Inst Gas Technology Pressure hydrogasification of natural gas liquids and petroleum distillates
US2867516A (en) * 1954-08-18 1959-01-06 Du Pont Process for burning gaseous fuels
US2982797A (en) * 1957-09-25 1961-05-02 Phillips Petroleum Co Catalyst regeneration and apparatus
US3055745A (en) * 1952-11-07 1962-09-25 Vulcan Cincinnati Inc Catalytic reactor
US3062197A (en) * 1959-07-23 1962-11-06 Selas Corp Of America Tube heater
US3069348A (en) * 1959-07-22 1962-12-18 Socony Mobil Oil Co Inc Multi-stage, multi-zone static bed reforming process and apparatus therefor
US3190812A (en) * 1960-01-22 1965-06-22 Ruetgerswerke Ag Device for the continuous production of hard pitch
US3198727A (en) * 1960-05-25 1965-08-03 Socony Mobil Oil Co Inc Quasi-isothermal hydrocarbon conversion and reactor therefor
US3285847A (en) * 1963-05-06 1966-11-15 Phillips Petroleum Co Fast thermal cracking of heavy carbonaceous materials
US4101376A (en) * 1974-03-18 1978-07-18 Metallgesellschaft Aktiengesellschaft Tubular heater for cracking hydrocarbons
US4454839A (en) * 1982-08-02 1984-06-19 Exxon Research & Engineering Co. Furnace
WO2015028123A1 (en) * 2013-08-26 2015-03-05 Thyssenkrupp Industrial Solutions Ag Collector conduit for common removal of process gases from a reformer which is supplied by a plurality of reformer tubes
WO2015075124A1 (en) * 2013-11-21 2015-05-28 Basf Se Method and device for carrying out endothermic reactions with formation of a fluidized layer in reaction tubes

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2456554A (en) * 1945-10-12 1948-12-14 United Carr Fastener Corp Connector for cords or cables
US2628890A (en) * 1946-06-20 1953-02-17 Hercules Powder Co Ltd Process for the decomposition of hydrocarbons
US2707147A (en) * 1948-02-07 1955-04-26 Hercules Powder Co Ltd Production of domestic gas
US2680061A (en) * 1951-02-07 1954-06-01 Columbian Carbon Carbon black
GB792827A (en) * 1954-02-19 1958-04-02 Hercules Powder Co Ltd Improvements in or relating to process for catalytic treatment of hydrocarbons
US2914386A (en) * 1954-12-20 1959-11-24 Hercules Powder Co Ltd Tubular furnace
FR2045712B1 (en) * 1969-06-25 1973-11-16 Onia Gegi
DE10023410A1 (en) * 2000-05-12 2001-11-15 Linde Gas Ag Production of carbon monoxide- and hydrogen-containing treatment gas comprises forming treatment gas for catalytically converting hydrocarbon gas in catalyst retort to which heat can be fed and varied over its length
DE10023409A1 (en) * 2000-05-12 2001-11-15 Linde Gas Ag Gas generator used for producing carbon monoxide- and hydrogen-containing treatment gas for heat treating metallic material comprises catalyst retort and device for heating partial regions of retort
DE10333854A1 (en) * 2003-07-24 2005-02-17 Uhde Gmbh Tubular cracking furnace used for reforming hydrocarbons e.g. to produce synthesis gas, comprises vertical cracker tubes, downward pointing burners and wedge shaped horizontal ceramic tunnels for removing flue gas
DE102007019830B3 (en) * 2007-04-25 2008-07-31 Uhde Gmbh Reactor for catalytic primary reformation of hydrocarbons with water vapor under increased pressure, has device for top firring of reformation process furnace, and supply mechanism, which has main inlet channel and secondary inlet channel

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2571953A (en) * 1947-09-19 1951-10-16 Hercules Powder Co Ltd Manufacture of hydrogen
US2660519A (en) * 1948-04-23 1953-11-24 Chemical Construction Corp Fluid heater
US2645566A (en) * 1949-12-12 1953-07-14 Gas Machinery Co High-temperature reactor
US2638407A (en) * 1949-12-31 1953-05-12 Standard Oil Dev Co Apparatus for close temperature control of catalyzed gas reactions
US2667410A (en) * 1950-01-04 1954-01-26 Phillips Petroleum Co Apparatus for reforming hydrocarbons
US2730434A (en) * 1950-05-01 1956-01-10 Oxy Catalyst Inc Catalytic contacting unit
US2743171A (en) * 1950-08-23 1956-04-24 United Gas Improvement Co Method for making gas rich in hydrogen
US2788266A (en) * 1951-10-13 1957-04-09 Stirnemann Ernst Catalytic reactor furnace
US3055745A (en) * 1952-11-07 1962-09-25 Vulcan Cincinnati Inc Catalytic reactor
US2852358A (en) * 1954-06-10 1958-09-16 Commercial Solvents Corp Process for reforming hydrocarbons
US2860959A (en) * 1954-06-14 1958-11-18 Inst Gas Technology Pressure hydrogasification of natural gas liquids and petroleum distillates
US2867516A (en) * 1954-08-18 1959-01-06 Du Pont Process for burning gaseous fuels
US2982797A (en) * 1957-09-25 1961-05-02 Phillips Petroleum Co Catalyst regeneration and apparatus
US3069348A (en) * 1959-07-22 1962-12-18 Socony Mobil Oil Co Inc Multi-stage, multi-zone static bed reforming process and apparatus therefor
US3062197A (en) * 1959-07-23 1962-11-06 Selas Corp Of America Tube heater
US3190812A (en) * 1960-01-22 1965-06-22 Ruetgerswerke Ag Device for the continuous production of hard pitch
US3198727A (en) * 1960-05-25 1965-08-03 Socony Mobil Oil Co Inc Quasi-isothermal hydrocarbon conversion and reactor therefor
US3285847A (en) * 1963-05-06 1966-11-15 Phillips Petroleum Co Fast thermal cracking of heavy carbonaceous materials
US4101376A (en) * 1974-03-18 1978-07-18 Metallgesellschaft Aktiengesellschaft Tubular heater for cracking hydrocarbons
US4454839A (en) * 1982-08-02 1984-06-19 Exxon Research & Engineering Co. Furnace
WO2015028123A1 (en) * 2013-08-26 2015-03-05 Thyssenkrupp Industrial Solutions Ag Collector conduit for common removal of process gases from a reformer which is supplied by a plurality of reformer tubes
CN105492378A (en) * 2013-08-26 2016-04-13 蒂森克虏伯工业解决方案股份公司 Collector conduit for common removal of process gases from a reformer which is supplied by a plurality of reformer tubes
CN105492378B (en) * 2013-08-26 2018-10-16 蒂森克虏伯工业解决方案股份公司 Collector vessel for removing the process gas from the reformer supplied by multiple reformer tubes jointly
WO2015075124A1 (en) * 2013-11-21 2015-05-28 Basf Se Method and device for carrying out endothermic reactions with formation of a fluidized layer in reaction tubes

Also Published As

Publication number Publication date
BE429915A (en)
DE887801C (en) 1953-08-27
USRE21521E (en) 1940-07-30

Similar Documents

Publication Publication Date Title
US2173984A (en) Apparatus and process for catalytic reactions
US2028326A (en) Apparatus for the production of hydrogen
US3607125A (en) Reformer tube construction
US3094391A (en) Hydrocarbon conversion
JP3075757B2 (en) Endothermic reactor
US2579843A (en) Method foe the manufacture of
US1909378A (en) Synthetic production of ammonia from a gaseous mixture of nitrogen and hydrogen in their combining proportions
US20230348277A1 (en) Reverse water gas shift catalytic reactor systems
US2467993A (en) Manufacture of formaldehyde and apparatus therefor
US3795485A (en) Synthesis gas generation apparatus
US2235401A (en) Gas generator for heat treating atmospheres
US3810975A (en) Start-up procedure for catalytic steam reforming of hydrocarbons
US3672847A (en) Reformer furnace
US2255126A (en) Method of controlling temperature of exothermic catalytic reactions
US2355753A (en) Catalytic apparatus
US3469946A (en) Apparatus for high-temperature conversions
US3202486A (en) Reaction vessel with refractory lining
GB1510697A (en) Supports for heat exchange tubes in furnaces
US2469329A (en) Apparatus for conducting reactions in the presence of a solid material
US2186590A (en) Process of heat treating gases
US2318688A (en) Regenerative furnace for manufacture of acetylene by pyrolysis
US2381306A (en) Gas generator unit
US1547167A (en) Process for the production of sulphuric acid
US1998401A (en) Catalyst roasting plant
JPS649358B2 (en)