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US3202664A - Method and apparatus for dealkylating and hydrogenation of organic compounds - Google Patents

Method and apparatus for dealkylating and hydrogenation of organic compounds Download PDF

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US3202664A
US3202664A US195799A US19579962A US3202664A US 3202664 A US3202664 A US 3202664A US 195799 A US195799 A US 195799A US 19579962 A US19579962 A US 19579962A US 3202664 A US3202664 A US 3202664A
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hydrogen
compounds
dealkylating
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gaseous
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US195799A
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Brooks James Douglas
Harrisson Raymond John
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Commonwealth Scientific and Industrial Research Organization CSIRO
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Commonwealth Scientific and Industrial Research Organization CSIRO
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
    • C07C1/20—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C4/00—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms
    • C07C4/08—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms by splitting-off an aliphatic or cycloaliphatic part from the molecule
    • C07C4/12—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms by splitting-off an aliphatic or cycloaliphatic part from the molecule from hydrocarbons containing a six-membered aromatic ring, e.g. propyltoluene to vinyltoluene
    • C07C4/14—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms by splitting-off an aliphatic or cycloaliphatic part from the molecule from hydrocarbons containing a six-membered aromatic ring, e.g. propyltoluene to vinyltoluene splitting taking place at an aromatic-aliphatic bond
    • C07C4/16—Thermal processes
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
    • C10G2400/30—Aromatics
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S585/00—Chemistry of hydrocarbon compounds
    • Y10S585/919—Apparatus considerations
    • Y10S585/92—Apparatus considerations using apparatus of recited composition

Definitions

  • the present invention relates to the hydrogenation of relatively complex organic compounds and their mixtures in the vapour phase to achieve simpler compounds.
  • the invention has particular application to the treatment of by-products from gas or coke production, oil refining, or other sources and also has wide application involving, for example, desulphurisation of organic compounds and substances.
  • the invention is based upon the discovery that organic materials when passed in the vapour phase together with hydrogen through a reaction vessel which contains a heated electrical resistance element undergo pyrolysis and/or destructive hydrogenation yielding products of simpler constitution.
  • tars may be treated in accordance with the invention in a vapourised condition directly from their source of production, intermediate handling being avoided.
  • the invention it is also possible to dealkylate alkyl aromatic compounds and simultaneously to reduce the content of sulphur-containing impurities, these being converted, for example, to hydrogen sulphide and carbon disulphide. Furthermore the invention may be used to reduce the amount of sulphur-containing impurities in organic compounds which do not contain an alkyl group for example, commercial benzene with a relatively high content of sulphur-containing compounds may be refined in this way.
  • One method of application of the invention consists in passing vapourised organic materials together with hydrogen through a reaction vessel in contact with a heated electrical resistance element, maintained at temperatures between 1000 C.-1500 C., the issuing vapours being collected and separated into desired fractions.
  • the process may be carried out at atmospheric or elevated pressures.
  • One form of the apparatus in accordance with the invention comprises a reaction vessel consisting of a tube either formed from or lined with a suitable heat resistant material (chemically inert under the conditions of reaction) through which extends one or more electrically heated tungsten or other suitable metal wires or a cylinder of platinum or other.
  • metal gauze located along or parallel to the longitudinal axis of said reaction vessel, the feed end of the reaction vessel communicating with sources of vapourised organic material and hydrogen and the outlet communicating with separation and storage facilities.
  • Table I eed material Product composition Toluene 92% benzene.
  • the operational temperature and rate of flow are variable to suit the starting materials and desired end prod net or products. Optimum conditions in any given case may be determined by routine test procedures.
  • the apparatus may be of any desired magnitude and will be constructed to suit operative conditions and quantities of materials to be handled.
  • FIGURE 1 shows one form of dealkylation reactor and equipment for recovering the products of the reaction
  • FIGURE 2 shows a modified form of the reactor illustrated in FIGURE 1, and
  • FIGURE 3 is a flow diagram showing how the apparatus in FIGURES 1 and 2 may be employed for the :direct treatment of tars and organic vapours at their source of production.
  • the liquid material to be treated in accordance with the invention is contained in liquid feed tank 1 and passes through fiow meter 2 into flash vaporizer 3.
  • the vaporized material then passes together with hydrogen (from flow meter 4) into dealkylation reactor 5 which comprises an industrial Pyrex tube thermally insulated as shown at 6 and carrying four tungsten Wires 7 on supporting rod 8, the tungsten wires being heated by a controllable power supply.
  • dealkylation reactor 5 which comprises an industrial Pyrex tube thermally insulated as shown at 6 and carrying four tungsten Wires 7 on supporting rod 8, the tungsten wires being heated by a controllable power supply.
  • the product from the dealkylation reactor passes through water cooled condenser 9 and the liquid condensate collects in catch pot 10 whilst uncondensed products are passed through chilled condenser 11 from which further liquid condensate may be removed at 12.
  • the remaining vapours then pass through electrostatic precipitator 13 and finally through scrubbing tower 14 through which chilled wash oil is downwardly
  • FIGURE 2 illustrates a flash vaporizer 16 with liquid feed inlet 17 and hydrogen inlet 18.
  • the vaporous products from the flash vaporizer then pass through dealkylation reactor 19 and the products of the reaction leave the reactor and go to the recovery plant at 20.
  • the heating element in the reactor 19 comprises a platinum or other suitable gauze cylinder 21 held in place by bracket 22, the cylinder being heated electrically via wire conduits 23.
  • FIGURE 3 shows the treatment of tars from for example a fluidized bed carbonization unit.
  • the tars together with the fluidizing gas containing hydrogen and with extra hydrogen if necessary pass through the dealkylation reactor, and the liquid products are condensed.
  • the gases containing methane, ethylene and acetylene may be reformed by known methods to yield hydrogen and carbon dioxide. After removal of the latter by established procedures, the hydrogen is led back into the fluidized bed carbonization unit. In a continuous process excess hydrogen may be drawn oil from the system.
  • the dealkylation process may be similarly operated in conjunction with other processes which yield alkylated aromatic compounds, for example processes employing petroleum-based feed stocks.
  • Acid-free Lurgi tar gave a product (43% yield) containing benzene (15%) naphthalene (23%) and polycyclic hydrocarbons (57%).
  • Petroleum solvent A containing 99.5% aromatic hydrocarbons, boiling range -215 C. gave a product (55% yield) containing benzene (53%) and naphthalene (l3 Petroleum solvent B, 42% aromatic hydrocarbons, boiling range 210280 C. gave a product (56%) containing benzene (26%) and naphthalene (50%).
  • Apparatus for dealkylating and hydrogenating gaseous organic compounds comprising an insulated tubular reaction vessel, a plurality of bare metallic filaments extending longitudinally through said reaction vessel, means for injecting gaseous admixture into said vessel and means for withdrawing gaseous admixture from said vessel.
  • Apparatus for dealkylating and hydrogenating gas- UNITED STATES PATENTS eous organic compounds comprising an insulated tubular 1,419,124 6/22 f m 260*672 reaction vessel having an internal Wall coating of meta- 5 1,654,654 1/28 Klrwm 196 121 phosphoric acid, metallic heating means extending longi- 1,857,814 5/32 Krauch et 196 121 tudinally through said reaction vessel, said heating means 2,395,161 2/46 Ashmore et a1 260 672 capable of being electrically heated to temperatures of 1000 to 1500" 0., means for injecting gaseous admixture WALTER MODANCE Primary Exammer' into said vessel and means for Withdrawing gaseous ad- 10 ALPHONSO D. SULLIVAN, NICHQLAS S. RIZZO, mixture from said vessel. Examiners.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Description

24, 1965 J D. BROOKS ETAL 3,202,664
METHOD AND APPARATUS FOR DEALKYLATING AND HYDROGENATION OF ORGANIC COMPOUNDS Filed May 18, 1962 3 Sheets-Sheet 1 4, 1965 J. D. BROOKS ETAL 3,292,664
METHOD AND APPARATUS FOR DEALKYLATING AND HYDROGENATION OF ORGANIC COMPOUNDS Filed May 18, 1962 3 Sheets-Sheet 2 F|G.2 A
Aug. 24, 1965 J. D. BROOKS ETAL METHOD AND APPARATUS FOR DEALKYLATING AND HYDROGENATION OF ORGANIC COMPOUNDS 3 Sheets-Sheet 5 Filed y United States Patent METHOD AND APPARATUS FOR DEALKYLATHNG AND HYDROGENATION OF ORGANIC COM- POUNDS James Douglas Brooks, Wahroonga, New South -Wales, and Raymond John Harrisson, llllrummoyne, New South Wales, Australia, assignors to Commonwealth Scientiiic and industrial Research Organization, East Melhourne, Victoria, Australia, a corporation or Australia Filed May 18, 1962, Ser. No. 195,7?9 Claims priority, application Australia, llliay 23, 1M1,
4,980/61 7 Claims. (Cl. 260-290) The present invention relates to the hydrogenation of relatively complex organic compounds and their mixtures in the vapour phase to achieve simpler compounds. The invention has particular application to the treatment of by-products from gas or coke production, oil refining, or other sources and also has wide application involving, for example, desulphurisation of organic compounds and substances.
The invention is based upon the discovery that organic materials when passed in the vapour phase together with hydrogen through a reaction vessel which contains a heated electrical resistance element undergo pyrolysis and/or destructive hydrogenation yielding products of simpler constitution.
In the case of by-products from gas or coke production which are complex mixtures of highly alkylated aromatic hydrocarbons, phenols and bases together with paraffinic and olefinic hydrocarbons and from which few industrially useful products can be easily isolated; valuable products can be simply and economically achieved with negligible formation of carbon or pitch. For example, benzene, naphthalene, phenol and pyridine, all of which have valuable industrial uses, are obtained from the different highly alkylated aromatic compounds mentioned above.
Additionally valuable gaseous products such as methane, ethylene and acetylene are produced and may be recovered. An important advantage of the invention is that tars may be treated in accordance with the invention in a vapourised condition directly from their source of production, intermediate handling being avoided.
By means of the invention it is possible to dealkylate alkyl aromatic compounds to give a very high yield of the parent aromatic compound, e.g. toluene is converted to benzene. Again straight chain compounds Whether saturated or unsaturated may be converted to methane and other products.
By means of the invention it is also possible to dealkylate alkyl aromatic compounds and simultaneously to reduce the content of sulphur-containing impurities, these being converted, for example, to hydrogen sulphide and carbon disulphide. Furthermore the invention may be used to reduce the amount of sulphur-containing impurities in organic compounds which do not contain an alkyl group for example, commercial benzene with a relatively high content of sulphur-containing compounds may be refined in this way.
The eifectiveness of the process is believed to be connected with the production of atomic hydrogen simultaneously with pyrolysis of organic compounds, providing an environment promoting dealkylation and other desired reactions.
It has been observed that in laboratory scale apparatus precautions were desirable to eliminate loss of atomic hydrogen by recombination of the hydrogen atoms on or "ice near the wall area of the reaction vessel. This requirement is not essential with preferred apparatus sufficiently large to avoid migration of hydrogen atoms to the wall region.
One method of application of the invention consists in passing vapourised organic materials together with hydrogen through a reaction vessel in contact with a heated electrical resistance element, maintained at temperatures between 1000 C.-1500 C., the issuing vapours being collected and separated into desired fractions. The process may be carried out at atmospheric or elevated pressures.
One form of the apparatus in accordance with the invention comprises a reaction vessel consisting of a tube either formed from or lined with a suitable heat resistant material (chemically inert under the conditions of reaction) through which extends one or more electrically heated tungsten or other suitable metal wires or a cylinder of platinum or other. metal gauze located along or parallel to the longitudinal axis of said reaction vessel, the feed end of the reaction vessel communicating with sources of vapourised organic material and hydrogen and the outlet communicating with separation and storage facilities.
The following examples, utilizing laboratory scale apparatus consisting essentially of a glass tube of about 1" diameter and 8 ft. in length through which is extended a tungsten wire electrically heated to temperatures of the order of 1200 C., the said tube having an internal wall coating or metaphosphoric acid which serves to diminish loss of atomic hydrogen, show the application of the invention to simple organic compounds.
The materials passed through the reaction vessel were collected and identified as indicated in the following Table 1.
Table I eed material: Product composition Toluene 92% benzene.
j90% benzenep 'MetwXyhne 8% toluene. }87% benzene. Para'xylne "111% toluene. l-methyl naphthalene 98% naphthalene. Scrubber naphtha benzene.
(Containing negligible quantities of benzene and naphthalene) 10% naphthalene.
47% benzene. 10% toluene. 15% phenol. 6% cyclopentadiene. 7% water. 3% naphthalene.
[5% hydrogen cyanide.
10% benzene.
20% pyridine.
30% methyl pyridines. [2% naphthalene.
The operational temperature and rate of flow are variable to suit the starting materials and desired end prod net or products. Optimum conditions in any given case may be determined by routine test procedures.
As an indication of the aspects of control of the process, it is pointed out that in dealkylating para or metaxylene a flow rate of added hydrogen of 250 ml./minute using the previously described laboratory apparatus gave Ortho-cresol benzene yields of 88 and 89% by weight. Doubling the flow rate reduced the yield by half and quadrupling it reduced the yield by more than a further half.
In general temperature control is predictable, too low a temperature giving poor conversion and too high a temperature giving rise to unwanted products e.g. condensation products such as diphenyl or in extreme conditions pitch and carbonaceous deposits.
It will be appreciated that the apparatus may be of any desired magnitude and will be constructed to suit operative conditions and quantities of materials to be handled.
The invention and more particularly its application to industrial uses will be more readily understood from the following description taken in conjunction with the accompanying drawings in which:
FIGURE 1 shows one form of dealkylation reactor and equipment for recovering the products of the reaction;
FIGURE 2 shows a modified form of the reactor illustrated in FIGURE 1, and
FIGURE 3 is a flow diagram showing how the apparatus in FIGURES 1 and 2 may be employed for the :direct treatment of tars and organic vapours at their source of production.
As shown in FIGURE 1 the liquid material to be treated in accordance with the invention is contained in liquid feed tank 1 and passes through fiow meter 2 into flash vaporizer 3. The vaporized material then passes together with hydrogen (from flow meter 4) into dealkylation reactor 5 which comprises an industrial Pyrex tube thermally insulated as shown at 6 and carrying four tungsten Wires 7 on supporting rod 8, the tungsten wires being heated by a controllable power supply. The product from the dealkylation reactor passes through water cooled condenser 9 and the liquid condensate collects in catch pot 10 whilst uncondensed products are passed through chilled condenser 11 from which further liquid condensate may be removed at 12. The remaining vapours then pass through electrostatic precipitator 13 and finally through scrubbing tower 14 through which chilled wash oil is downwardly passed. The gases are passed through gas meter 15 and then collected.
FIGURE 2 illustrates a flash vaporizer 16 with liquid feed inlet 17 and hydrogen inlet 18. The vaporous products from the flash vaporizer then pass through dealkylation reactor 19 and the products of the reaction leave the reactor and go to the recovery plant at 20. The heating element in the reactor 19 comprises a platinum or other suitable gauze cylinder 21 held in place by bracket 22, the cylinder being heated electrically via wire conduits 23.
FIGURE 3 shows the treatment of tars from for example a fluidized bed carbonization unit. The tars together with the fluidizing gas containing hydrogen and with extra hydrogen if necessary pass through the dealkylation reactor, and the liquid products are condensed. The gases containing methane, ethylene and acetylene may be reformed by known methods to yield hydrogen and carbon dioxide. After removal of the latter by established procedures, the hydrogen is led back into the fluidized bed carbonization unit. In a continuous process excess hydrogen may be drawn oil from the system. The dealkylation process may be similarly operated in conjunction with other processes which yield alkylated aromatic compounds, for example processes employing petroleum-based feed stocks.
Examples of the treatment of industrial feed stocks are as follows:
Vertical retort tar naphtha, boiling range 190-210 0.,
containing saturated hydrocarbons (18%), olefinic hydrocarbons (14%) and aromatic hydrocarbons (65%, in-
cluding naphthalene, 25%) gave a product (74% yield) containing benzene (31%) and naphthalene (66% Vertical retort tar middle oil, boiling range ZOO-290 C., containing saturated hydrocarbons (19%), olefinic hydrocarbons (20%) and aromatic hydrocarbons (61%) gave a product (40% yield) containing benzene (22%) and naphthalene (66%).
Acid-free low-temperature tar, of which boiled below 400 C. gave a product (32% yield) containing benzene (25%), naphthalene (12%) and polycyclic hydrocarbons (62%).
Acid-free Lurgi tar gave a product (43% yield) containing benzene (15%) naphthalene (23%) and polycyclic hydrocarbons (57%).
Petroleum solvent A, containing 99.5% aromatic hydrocarbons, boiling range -215 C. gave a product (55% yield) containing benzene (53%) and naphthalene (l3 Petroleum solvent B, 42% aromatic hydrocarbons, boiling range 210280 C. gave a product (56%) containing benzene (26%) and naphthalene (50%).
Petroleum solvent C containing 82% aromatic hydrocarbons (33% naphthalene) boiling range 80-240 C. gave a product (57% yield) containing benzene (17%) and naphthalene (63%).
In the foregoing description where reference is made to hydrogen it is to be understood that hydrogen containing gases including coal gas, town gas or water gas are effective for the purposes of the invention.
What We claim is:
1. Process for dealkylating and hydrogenating gaseous by-product compounds from gas and coke production, said by-products comprising alkyl aromatic hydrocarbons, alkyl phenols, and alkyl aromatic bases admixed with paraifinic and olefinic hydrocarbons, comprising (1) mixing said compounds in the gaseous state with molecular hydrogen,
(2) contacting the resultant gaseous admixture with metallic filament in a reaction zone while concomitantly maintaining said zone at a temperature sufficiently high to prevent condensation of organic vapors, said filament being heated to a temperature between 1000 and 1500 C., whereby atomic hydrogen is formed at said filament, and
(3) condensing the resultant dealkylated product.
2. Process for dealkylating and hydrogenating an admixture of alkyl cyclic compounds comprising (1) mixing said compounds in the gaseous state with molecular hydrogen,
(2) contacting the resultant gaseous admixture with metallic filament in a reaction zone, while concomitantly maintaining said zone at a temperature sufiiciently high to prevent condensation of organic vapors, said filament being heated to a temperature between 1000 and 1500 C., whereby atomic hydrogen is formed at said filament, and
(3) condensing the resultant dealkylated product.
3. Process for dealkylating an alkylated aromatic compound comprising (1) mixing said compounds in the gaseous state with molecular hydrogen,
(2) contacting the resultant gaseous admixture with metallic filament in a reaction zone while concomitantly maintaining said zone at a temperature sufficiently high to prevent condensation of organic vapors, said filament being heated to a temperature between 1000 and 1500 C., whereby atomic hydrogen is formed at said filament, and
(3) condensing the resultant dealkylated product.
4. Apparatus for dealkylating and hydrogenating gaseous organic compounds comprising an insulated tubular reaction vessel, a plurality of bare metallic filaments extending longitudinally through said reaction vessel, means for injecting gaseous admixture into said vessel and means for withdrawing gaseous admixture from said vessel.
5. Apparatus of claim 4 wherein said vessel is lined with material chemically inert at temperatures of reaction.
6. Apparatus of claim 4 wherein said vessel is com- 5 6 posed of material chemically inert at temperatures of References Cited by the Examiner reaction.
7. Apparatus for dealkylating and hydrogenating gas- UNITED STATES PATENTS eous organic compounds comprising an insulated tubular 1,419,124 6/22 f m 260*672 reaction vessel having an internal Wall coating of meta- 5 1,654,654 1/28 Klrwm 196 121 phosphoric acid, metallic heating means extending longi- 1,857,814 5/32 Krauch et 196 121 tudinally through said reaction vessel, said heating means 2,395,161 2/46 Ashmore et a1 260 672 capable of being electrically heated to temperatures of 1000 to 1500" 0., means for injecting gaseous admixture WALTER MODANCE Primary Exammer' into said vessel and means for Withdrawing gaseous ad- 10 ALPHONSO D. SULLIVAN, NICHQLAS S. RIZZO, mixture from said vessel. Examiners.

Claims (1)

1. PROCESS FOR DEALKYLATING AND HYDROGENATING GASEOUS BY-PRODUCT COMPOUNDS FROM GAS AND COKE PRODUCTION, SAID BY-PRODUCTS COMPRISING ALKYL AROMATIC HYDROCARBONS, ALKYL PHENOLS, AND ALKYL AROMATIC BASES ADMIXED WITH PARAFFINIC AND OLEFINIC HYDROCARBONS, COMPRISING (1) MIXING SAID COMPOUNDS IN THE GASEOUS STATE WITH MOLECULAR HYDROGEN, (2) CONTACTING THE RESULTANT GASEOUS ADMIXTURE WITH METALLIC FILAMENT IN A REACTION ZONE WHILE CONCOMITANTLY MAINTAINING SAID ZONE AT A TEMPERATURE SUFFICIENTLY HIGH TO PREVENT CONDENSATION OF ORGANIC VAPORS, SAID FILAMENT BEING HEATED TO A TEMPERATURE BETWEEN 1000 AND 1500*C., WHEREBY ATOMIC HYDROGEN IS FORMED AT SAID FILAMENT, AND (3) CONDENSING THE RESULTANT DEALKYLATED PRODUCT.
US195799A 1961-05-23 1962-05-18 Method and apparatus for dealkylating and hydrogenation of organic compounds Expired - Lifetime US3202664A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3442793A (en) * 1966-12-30 1969-05-06 Universal Oil Prod Co Method for hydrocarbon conversion
US4205017A (en) * 1978-06-19 1980-05-27 Phillips Petroleum Company Hydrodehydroxylation process using a rhenium-fluorided alumina catalyst
US20230144856A1 (en) * 2020-03-13 2023-05-11 University Of Maryland, College Park High-temperature shock heating for thermochemical reactions

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1419124A (en) * 1922-06-06 Treatment of xylene and other- similar hydrocarbons
US1654654A (en) * 1925-10-09 1928-01-03 Roscoe C Kirwin Apparatus for treating hydrocarbon liquids
US1857814A (en) * 1926-07-28 1932-05-10 Standard L G Company Supplying heat in high pressure reactions
US2395161A (en) * 1942-04-08 1946-02-19 Ashmore Stanley Arthur Production of xylene and toluene and other light coal tar oils

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1419124A (en) * 1922-06-06 Treatment of xylene and other- similar hydrocarbons
US1654654A (en) * 1925-10-09 1928-01-03 Roscoe C Kirwin Apparatus for treating hydrocarbon liquids
US1857814A (en) * 1926-07-28 1932-05-10 Standard L G Company Supplying heat in high pressure reactions
US2395161A (en) * 1942-04-08 1946-02-19 Ashmore Stanley Arthur Production of xylene and toluene and other light coal tar oils

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3442793A (en) * 1966-12-30 1969-05-06 Universal Oil Prod Co Method for hydrocarbon conversion
US4205017A (en) * 1978-06-19 1980-05-27 Phillips Petroleum Company Hydrodehydroxylation process using a rhenium-fluorided alumina catalyst
US20230144856A1 (en) * 2020-03-13 2023-05-11 University Of Maryland, College Park High-temperature shock heating for thermochemical reactions

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