GB1011294A - Production of hydrogen-containing gases from liquid hydrocarbon - Google Patents
Production of hydrogen-containing gases from liquid hydrocarbonInfo
- Publication number
- GB1011294A GB1011294A GB22976/63A GB2297663A GB1011294A GB 1011294 A GB1011294 A GB 1011294A GB 22976/63 A GB22976/63 A GB 22976/63A GB 2297663 A GB2297663 A GB 2297663A GB 1011294 A GB1011294 A GB 1011294A
- Authority
- GB
- United Kingdom
- Prior art keywords
- steam
- hydrocarbon
- zone
- melt
- mixed
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
- C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
- C01B3/32—Production 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
- C01B3/34—Production 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
- C01B3/348—Production 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 by direct contact with heat accumulating liquids, e.g. molten metals, molten salts
-
- 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
- C10G2400/26—Fuel gas
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)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Hydrogen, Water And Hydrids (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A process for producing a hydrogen-containing gas from a normally liquid hydrocarbon, i.e. one having atmospheric pressure boiling points above 100 DEG F., comprises contacting the hydrocarbon and steam with an alkali metal compound in the molten state. The compound may comprise one or more of the alkali metal carbonates, hydroxides, nitrates, sulphides and oxides, or an alkali metal compound convertible under the reaction conditions to an equilibrium mixture of the carbonate and hydroxide, e.g. sulphates or chlorides. Alkaline earth metal carbonates, hydroxides and oxides may be added. The reaction temperature ranges from 800 DEG to 1800 DEG F., and pressures from 14 to 1000 p.s.i.a., preferably from 50 to 850 p.s.i.a. The hydrocarbon and steam may be bubbled up through a molten pool of the salt in the reaction zone, or they may be charged separately or in admixture to one or more points in the zone, and further, the salt may be sprayed or trickled into the zone. Where they are mixed, the hydrocarbon may be preheated, e.g. to 200 DEG to 800 DEG F., and mixed with preheated steam, or mixed unheated with superheated steam. Steam/carbon ratios (i.e. mols steam per atom of carbon) of 1 to 20 are mentioned. The melt may be circulated between the reaction zone and a heating zone, or the reaction zone may be suitably heated. In one embodiment, hydrocarbon and nitrogen was delivered through a central tube and steam through an outer annular tube, the combined streams being sprayed into the melt, a perforated cone deflector at the top of the reactor preventing salt being entrained in the gas produced. Two specific examples are described using the above apparatus and employing Mid-continent gas oil, and melts comprising respectively (by weight) 15% and 19% lithium carbonate, balance sodium carbonate. Many hydrocarbon starting materials are mentioned, and an ash-rich stream may be withdrawn from the melt.ALSO:A process for producing a hydrogen-containing gas from a normally liquid hydrocarbon, i.e. one having atmospheric pressure boiling points above 100 DEG F., comprises contacting the hydrocarbon and steam with an alkali metal compound in the molten state. The compound may comprise one or more of the alkali metal carbonates, hydroxides, nitrates, sulphides and oxides, or an alkali metal compound convertible under the reaction conditions to an equilibrium mixture of the carbonate and hydroxide, e.g. sulphates or chlorides. Alkaline earth metal carbonates, hydroxides and oxides may be added. The reaction temperature ranges from 800 DEG to 1800 DEG F., and pressures from 14 to 1000 p.s.i.a., preferably from 50 to 850 p.s.i.a. The hydrocarbon and steam may be bubbled up through a molten pool of the salt in the reaction zone, or they may be charged separately or in admixture to one or more points in the zone, and further, the salt may be sprayed or trickled into the zone. Where they are mixed, the hydrocarbon may be preheated, e.g. to 200 DEG to 800 DEG F., and mixed with preheated steam, or mixed unheated with superheated steam. Steam/carbon ratios (i.e. mols steam per atom of carbon) of 1 to 20 are mentioned. The melt may be circulated between the reaction zone and a heating zone, or the reaction zone may be suitably heated. In one embodiment, hydrocarbon and nitrogen was delivered through a central tube and steam through an outer annular tube, the combined streams being sprayed into the melt, a perforated cone deflector at the top of the reactor preventing salt being entrained in the gas produced. Two specific examples are described using the above apparatus and employing mid-continent gas oil, and melts comprising respectively (by weight) 15% and 19% lithium carbonate, balance sodium carbonate. Many hydrocarbon starting materials are mentioned, and an ashrich stream may be withdrawn from the melt.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201248A US3252774A (en) | 1962-06-11 | 1962-06-11 | Production of hydrogen-containing gases |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1011294A true GB1011294A (en) | 1965-11-24 |
Family
ID=22745095
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB22976/63A Expired GB1011294A (en) | 1962-06-11 | 1963-06-10 | Production of hydrogen-containing gases from liquid hydrocarbon |
Country Status (3)
Country | Link |
---|---|
US (1) | US3252774A (en) |
DE (1) | DE1470714B1 (en) |
GB (1) | GB1011294A (en) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3453146A (en) * | 1966-01-03 | 1969-07-01 | Texas Instruments Inc | Method and apparatus for reforming carbonaceous fuels and operating fuel cell |
US3838993A (en) * | 1971-03-18 | 1974-10-01 | Exxon Research Engineering Co | Two stage process for the conversion of heavy hydrocarbons to a methane rich gas stream |
US3770399A (en) * | 1971-10-22 | 1973-11-06 | Sun Research Development | Coal gasification process |
US3838994A (en) * | 1972-02-14 | 1974-10-01 | Exxon Research Engineering Co | Conversion of heavy hydrocarbons to a methane rich gas product |
US3929431A (en) * | 1972-09-08 | 1975-12-30 | Exxon Research Engineering Co | Catalytic reforming process |
JPS5948078B2 (en) * | 1978-02-13 | 1984-11-24 | 三井化学株式会社 | Heavy oil pyrolysis method |
JPS55102684A (en) * | 1979-01-06 | 1980-08-06 | Mitsui Eng & Shipbuild Co Ltd | Thermal cracking of hydrocarbon and its device |
US4366045A (en) * | 1980-01-22 | 1982-12-28 | Rollan Swanson | Process for conversion of coal to gaseous hydrocarbons |
DE3114766A1 (en) * | 1980-04-15 | 1982-06-16 | Rollan Dr. 89316 Eureka Nev. Swanson | METHOD FOR CONVERTING COAL OR Peat TO GASEOUS HYDROCARBONS OR VOLATILE DISTILLATES OR MIXTURES THEREOF |
US4606812A (en) * | 1980-04-15 | 1986-08-19 | Chemroll Enterprises, Inc. | Hydrotreating of carbonaceous materials |
FR2509634B1 (en) * | 1981-07-20 | 1986-10-10 | Cirta Ct Int Rech Tech Appliqu | PROCESS FOR THE DESTRUCTION OF ORGANIC MATERIALS CONTAINING SULFUR AND / OR HALOGENS AND APPLICATIONS THEREOF |
US4421631A (en) * | 1981-10-02 | 1983-12-20 | Rockwell International Corporation | Hydrocarbon treatment process |
US4468316A (en) * | 1983-03-03 | 1984-08-28 | Chemroll Enterprises, Inc. | Hydrogenation of asphaltenes and the like |
US5537940A (en) * | 1993-06-08 | 1996-07-23 | Molten Metal Technology, Inc. | Method for treating organic waste |
US6994839B2 (en) * | 2001-08-15 | 2006-02-07 | Ovonic Battery Company, Inc. | Carbonate recycling in a hydrogen producing reaction |
US7588676B2 (en) * | 2004-01-23 | 2009-09-15 | Ovonic Battery Company, Inc. | Base-facilitated production of hydrogen from carbonaceous matter |
US7862707B2 (en) * | 2007-02-18 | 2011-01-04 | David Rendina | Liquid fuel feedstock production process |
US8309049B2 (en) * | 2009-10-19 | 2012-11-13 | Battelle Energy Alliance, Llc | Molten metal reactor and method of forming hydrogen, carbon monoxide and carbon dioxide using the molten alkaline metal reactor |
US8685281B2 (en) * | 2011-07-21 | 2014-04-01 | Battelle Energy Alliance Llc | System and process for the production of syngas and fuel gasses |
US9216401B2 (en) * | 2011-07-21 | 2015-12-22 | Battelle Energy Alliance Llc | Bell column downtube, reactors utilizing same and related methods |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US701186A (en) * | 1901-07-25 | 1902-05-27 | William J Faulkner | Apparatus for generating gas. |
GB191007718A (en) * | 1909-07-07 | 1911-03-30 | Otto Dieffenbach | Improvements in the Production of Hydrogen. |
GB322959A (en) * | 1929-02-20 | 1929-12-19 | Theodor Lichtenberger | A process for the extraction of gases from and for the gasification of fuels |
GB334241A (en) * | 1929-05-30 | 1930-09-01 | Bataafsche Petroleum | Improvements in or relating to the cracking of hydrocarbons |
US2015085A (en) * | 1930-05-14 | 1935-09-24 | Oberle Alfred | Method of thermolizing carbonizable materials |
US2031987A (en) * | 1934-09-13 | 1936-02-25 | Standard Oil Co | Conversion of hydrocarbons |
GB465548A (en) * | 1936-07-06 | 1937-05-10 | Theodor Lichtenberger | An improved process for obtaining water gas |
US2628890A (en) * | 1946-06-20 | 1953-02-17 | Hercules Powder Co Ltd | Process for the decomposition of hydrocarbons |
US2794709A (en) * | 1952-12-20 | 1957-06-04 | Houdry Process Corp | Preparation of carbon black and hydrogen |
GB769021A (en) * | 1954-06-18 | 1957-02-27 | North Thames Gas Board | Improvements in or relating to the production of combustible gases from petroleum oil |
-
1962
- 1962-06-11 US US201248A patent/US3252774A/en not_active Expired - Lifetime
-
1963
- 1963-06-10 GB GB22976/63A patent/GB1011294A/en not_active Expired
- 1963-06-11 DE DE19631470714D patent/DE1470714B1/en active Pending
Also Published As
Publication number | Publication date |
---|---|
US3252774A (en) | 1966-05-24 |
DE1470714B1 (en) | 1970-07-09 |
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