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US1592474A - Process for the thermal decomposition of gaseous hydrocarbons, natural gas, or the like by heat - Google Patents

Process for the thermal decomposition of gaseous hydrocarbons, natural gas, or the like by heat Download PDF

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US1592474A
US1592474A US694808A US69480824A US1592474A US 1592474 A US1592474 A US 1592474A US 694808 A US694808 A US 694808A US 69480824 A US69480824 A US 69480824A US 1592474 A US1592474 A US 1592474A
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decomposition
chamber
walls
natural gas
heat
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US694808A
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Szarvasy Imre
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09CTREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C1/00Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/44Carbon
    • C09C1/48Carbon black
    • C09C1/54Acetylene black; thermal black ; Preparation thereof
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S48/00Gas: heating and illuminating
    • Y10S48/05Diffusion membrane for gas reaction or separation

Definitions

  • PROCESS 103 THE THERMAL DECOMPOSITION OF GASEOUS HYDROOARBONS, NATURAL GAS, OR THE LIKE BY HEAT.
  • This invention relates to a rocess of decomposing gaseous hydrocar ons, such as natural gas or the like, by heat.
  • the retort is glazed, the cost of production is increased, and o portunity for the reduction of silicic acid is atforded.
  • the retort is constructed of a material of a 'orcelainlike character sintering only at a igh temperature waste takes lace when firing the retorts or chambers w ich are generally of considerable length, 5-6 metres in consequence of their great shrinkage and deformation, and thus an increase in the cost of production is unavoidable.
  • such retorts had to be provided with wa ls of comparatively considerable thickness and thus an inferior heat transference had to be taken into account.
  • retorts with as-tight walls were very sensitive in practice owing to the fluctuations in temperature caused by draughts of air or jets of flame.
  • the invention enables the aforesaid disadvantage to be obviated and to this end consists essentially in effecting one part of the heating of the decomposition chambers in a known manner by means of the products of decomposition led from the decomposition chambers through conduits-and if desired heating chamber, whilst efl'ecting the other part by means of the decomposition gases, passed directly from the decomposition .chamber through the walls thereof.
  • the walls 6 have been made of material which is as ti ht as possible, and the process has beenconducted in such a way as to allow no gas to pass from one chamber into the other.
  • the latter is effectively protected against fluctuations of temperature.
  • the uniformity of the heating is moreover ensured by the fact that the deposition of carbon takes place more slowly at the moderately heated parts of the chamber walls so that the free cross section of the openings, and the corres onding amount of gas passing theret rou h remains larger at those parts, so that t e chamber is there heated to a higher degree than at the originally hotter parts.
  • the temperature of the walls is automatically equalized by the decomposition of the aseous hydrocarbons, natural gas or the 11 e and subsequent deposition of carbon.
  • the walls of the chamber or retort can be constructed of porous material or of porous carbon.
  • the process is in this case carried out substantially in accordance with the example above-described. Inasmuch, however, as the distribution and the number of pores is more uniform and greater than those of the artificial openings, the heating of the retort by the difiusing gases will also be more uniform.
  • Such retorts with porous walls are not only essentially cheaper than those of gas-tight material with artificial openings, but are also considerably more durable in practice.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Description

I ZARVASY PROCESS FOR THE THERMAL DE MPOS ON OF GASEOUS HYDROCARBONS,
NATURAL GAS, LIKE BY HEAT Filed .7 23, 1924 Patented July 13, 1926.
PATENT OFFICE.
SZARVASY, F BUDAPEST, HUNGARY.
PROCESS 103 THE THERMAL DECOMPOSITION OF GASEOUS HYDROOARBONS, NATURAL GAS, OR THE LIKE BY HEAT.
Application fled February 28, 1924, Serial No. 694,808, and in Hungary November 15, 1983.
This invention relates to a rocess of decomposing gaseous hydrocar ons, such as natural gas or the like, by heat.
When efiectin the decomposition of gaseous hydrocar ons, natural gas of the like in ractice by heat, in order for exampleto obtain soot (carbon black), electrodecarbon, and the like the aim has always been to make thewalls separating the heat- 10 ing chamber from the decomposition chamthrough regeneratorsinto the ber, for example the retort walls or chamber walls, as tight as possible, in order on the one hand to prevent the inflow of air or heating gases into the decomposition chamber, and on the other hand to prevent the decomposed gas from entering the heating cham- The use of retorts or chambers with gastight walls is however attended with many disadvantages. If the retort is glazed, the cost of production is increased, and o portunity for the reduction of silicic acid is atforded. If, on the other hand, the retort is constructed of a material of a 'orcelainlike character sintering only at a igh temperature waste takes lace when firing the retorts or chambers w ich are generally of considerable length, 5-6 metres in consequence of their great shrinkage and deformation, and thus an increase in the cost of production is unavoidable. Moreover owing to such srinka e, such retorts had to be provided with wa ls of comparatively considerable thickness and thus an inferior heat transference had to be taken into account. Finally retorts with as-tight walls were very sensitive in practice owing to the fluctuations in temperature caused by draughts of air or jets of flame.
The invention enables the aforesaid disadvantage to be obviated and to this end consists essentially in effecting one part of the heating of the decomposition chambers in a known manner by means of the products of decomposition led from the decomposition chambers through conduits-and if desired heating chamber, whilst efl'ecting the other part by means of the decomposition gases, passed directly from the decomposition .chamber through the walls thereof.
In order to understand more clearly the inchamber 1 is heated. The
V of the gaseous hydrocarbons,
vention reference is made to the accompanying drawing which shows a diagrammatic:
Whilst the decomposition ases are conducted into the heating chain or 5 through the conduit 4, and are there burnt in admixture with air, whereby the wall 6 separating the heating chamber 5 from the decomposition gases are finally conducted away through the flue 7.
Hitherto the walls 6 have been made of material which is as ti ht as possible, and the process has beenconducted in such a way as to allow no gas to pass from one chamber into the other.
It is however possible to provide the walls of the decomposition chambers with openings and to supply the gaseous h drocarbons,- natural gas or the like to the ecomposition chamber at a higher pressure than that of the heating chamber so that initially part natural gas or the like flows directly through the perforations of the walls into the heating chamber 1 where it burns in immediate proximity of the walls, thus heating the decomposition chamber to the desired temperature.
In consequence of'thermal decomposition the openings are gradually blocked by the carbon, so that after some time practically no more undecomposed gaseous hydrocarbons, natural gas or the like can escape through the openings of the walls into the heating chamber. However hydrogen still difl'uses into the heating chamber through the openings blocked by porous carbon and burns in immediate proximity of the walls of the decomposition chamber in the same way as before, whilst the excess of decomposition gases flows in a manner known per se from the decomposition chamber through conduits, into the heating chamber, to which naturally a corresponding amount of combustion air must be supplied.
Inasmuch as part ofthe decomposition gases burns in immediate proximity of the walls of the decomposition chamber their heating power is utilized to advantage. Moreover since this part of the decomposition gases forms a glowing gaseous shell surroundin the entire decomposition vessel,
the latter is effectively protected against fluctuations of temperature. The uniformity of the heating is moreover ensured by the fact that the deposition of carbon takes place more slowly at the moderately heated parts of the chamber walls so that the free cross section of the openings, and the corres onding amount of gas passing theret rou h remains larger at those parts, so that t e chamber is there heated to a higher degree than at the originally hotter parts. Thus the temperature of the walls is automatically equalized by the decomposition of the aseous hydrocarbons, natural gas or the 11 e and subsequent deposition of carbon.
Instead of providing the walls of the chamber or retort with artificial openings, they can be constructed of porous material or of porous carbon. The process is in this case carried out substantially in accordance with the example above-described. Inasmuch, however, as the distribution and the number of pores is more uniform and greater than those of the artificial openings, the heating of the retort by the difiusing gases will also be more uniform. Such retorts with porous walls are not only essentially cheaper than those of gas-tight material with artificial openings, but are also considerably more durable in practice.
Whilst I have hereinbefore described only the preferred wa of carrying out the present process it s ould bewell understood that many changes and modifications may be made therein without departing from the spirit and scope of the invention as defined by the appended claims.
Having now particularly described and ascertained the nature of my said invention and in what manner the same is to be performed, I declare that what I claim is:
1. In the manufacture of useful products by decomposition of gaseous hydrocarbons of the character described, by heat in decomposition chambers the walls of which separate said decomposition chambers from the heating chamber and are heated by the combustion of the decomposition gases conducted from said decomposition chamber to said heating chamber, the process which comprises passing at least one part of the decomposition gases directly through the walls of the decomposing chamber and burning said gases in said heating chamber.
2. In the manufacture of useful products by decomposition of gaseous hydrocarbons of the character described, by heat in decomposition chambers the walls of which separate said decomposition chambers from the heating chamber and are heated by the combustion of the decomposition-gases conducted from said decomposition chamber to said heating chamber, the process which comprises passing from the decomposition chamer one part of the decomposition gases admixed with solid decomposition products, passing the other part of the decomposition gases free of solid admixtures, directly through the walls of the decomposing chamber, and burning said gases in immediate proximity to said walls.
3. In the manufacture of useful products by thermal decomposition of gaseous hydrocarbons of the character described, the process which comprises passing the seous hydrocarbons into a decomposing c amber maintained at a decomposing temperature and provided with pervious walls, and heating said chamber at least in part by means ofcombustible gases passing from said chamber through said walls and burning in immediate proximity thereto.
In testimony whereof I aflix my signature.
IMRE szAizvAsY.
US694808A 1923-11-15 1924-02-23 Process for the thermal decomposition of gaseous hydrocarbons, natural gas, or the like by heat Expired - Lifetime US1592474A (en)

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2436282A (en) * 1943-03-26 1948-02-17 Continental Oil Co Surface combustion cracking furnace
US2516974A (en) * 1946-12-04 1950-08-01 Texace Dev Corp Method and apparatus for gasifying carbonaceous material
US2614066A (en) * 1949-05-10 1952-10-14 Gulf Oil Corp Hydrodesulfurization of petroleum hydrocarbons
US2649360A (en) * 1949-01-24 1953-08-18 Jefferson Lake Sulphur Co Carbon black furnaces
US2772149A (en) * 1951-12-13 1956-11-27 Hydrocarbon Research Inc Generation of synthesis gas and apparatus therefor
US2885269A (en) * 1957-07-05 1959-05-05 Commercial Solvents Corp Continuously heated carbon black furnace
US3290406A (en) * 1962-05-15 1966-12-06 Engelhard Ind Inc Process for dehydrogenation

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2436282A (en) * 1943-03-26 1948-02-17 Continental Oil Co Surface combustion cracking furnace
US2516974A (en) * 1946-12-04 1950-08-01 Texace Dev Corp Method and apparatus for gasifying carbonaceous material
US2649360A (en) * 1949-01-24 1953-08-18 Jefferson Lake Sulphur Co Carbon black furnaces
US2614066A (en) * 1949-05-10 1952-10-14 Gulf Oil Corp Hydrodesulfurization of petroleum hydrocarbons
US2772149A (en) * 1951-12-13 1956-11-27 Hydrocarbon Research Inc Generation of synthesis gas and apparatus therefor
US2885269A (en) * 1957-07-05 1959-05-05 Commercial Solvents Corp Continuously heated carbon black furnace
US3290406A (en) * 1962-05-15 1966-12-06 Engelhard Ind Inc Process for dehydrogenation

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