US1945960A - Production of hydrocarbons - Google Patents
Production of hydrocarbons Download PDFInfo
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- US1945960A US1945960A US516829A US51682931A US1945960A US 1945960 A US1945960 A US 1945960A US 516829 A US516829 A US 516829A US 51682931 A US51682931 A US 51682931A US 1945960 A US1945960 A US 1945960A
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- hydrocarbons
- methane
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- 229930195733 hydrocarbon Natural products 0.000 title description 29
- 150000002430 hydrocarbons Chemical class 0.000 title description 29
- 238000004519 manufacturing process Methods 0.000 title description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 27
- 239000007789 gas Substances 0.000 description 14
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 10
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 8
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical class [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 239000010949 copper Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 229910052710 silicon Inorganic materials 0.000 description 7
- 239000010703 silicon Substances 0.000 description 7
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- 229910052802 copper Inorganic materials 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
- 239000005977 Ethylene Substances 0.000 description 5
- 239000005864 Sulphur Substances 0.000 description 5
- 238000009835 boiling Methods 0.000 description 5
- 239000001273 butane Substances 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 5
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 5
- 239000001294 propane Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 4
- 239000000956 alloy Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- -1 ethylene, propylene Chemical group 0.000 description 4
- 239000012263 liquid product Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229910001385 heavy metal Inorganic materials 0.000 description 3
- 239000007769 metal material Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 230000000737 periodic effect Effects 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- 229910001316 Ag alloy Inorganic materials 0.000 description 2
- 229910001020 Au alloy Inorganic materials 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 230000001427 coherent effect Effects 0.000 description 2
- HPDFFVBPXCTEDN-UHFFFAOYSA-N copper manganese Chemical compound [Mn].[Cu] HPDFFVBPXCTEDN-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000011133 lead Substances 0.000 description 2
- 239000010687 lubricating oil Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 239000011863 silicon-based powder Substances 0.000 description 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 2
- HCUOEKSZWPGJIM-YBRHCDHNSA-N (e,2e)-2-hydroxyimino-6-methoxy-4-methyl-5-nitrohex-3-enamide Chemical compound COCC([N+]([O-])=O)\C(C)=C\C(=N/O)\C(N)=O HCUOEKSZWPGJIM-YBRHCDHNSA-N 0.000 description 1
- JQMFQLVAJGZSQS-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-N-(2-oxo-3H-1,3-benzoxazol-6-yl)acetamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)NC1=CC2=C(NC(O2)=O)C=C1 JQMFQLVAJGZSQS-UHFFFAOYSA-N 0.000 description 1
- 101100162200 Aspergillus parasiticus (strain ATCC 56775 / NRRL 5862 / SRRC 143 / SU-1) aflD gene Proteins 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 229910000906 Bronze Inorganic materials 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 235000010582 Pisum sativum Nutrition 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 239000010974 bronze Substances 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- VNNRSPGTAMTISX-UHFFFAOYSA-N chromium nickel Chemical compound [Cr].[Ni] VNNRSPGTAMTISX-UHFFFAOYSA-N 0.000 description 1
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000000266 injurious effect Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- VYMDGNCVAMGZFE-UHFFFAOYSA-N phenylbutazonum Chemical compound O=C1C(CCCC)C(=O)N(C=2C=CC=CC=2)N1C1=CC=CC=C1 VYMDGNCVAMGZFE-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 235000002020 sage Nutrition 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000002912 waste gas Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/02—Apparatus characterised by being constructed of material selected for its chemically-resistant properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/02—Apparatus characterised by their chemically-resistant properties
- B01J2219/025—Apparatus characterised by their chemically-resistant properties characterised by the construction materials of the reactor vessel proper
- B01J2219/0277—Metal based
- B01J2219/0286—Steel
-
- 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
- Y10S585/929—Special chemical considerations
- Y10S585/943—Synthesis from methane or inorganic carbon source, e.g. coal
Definitions
- This invention relates to improvements in the utacture and production of hydrocarbons from gaseous or vaporous hydrocarbons of the methane series.
- Unsaturated hydrocarbons such as ethylene, propylene and the like, may be readily converted into valuable liquid hydrocarbons, such as benzone and benzine, without any injurious deposition of carbon by employing as catalysts heavy metals of group 1 of the periodic system, namely gold, silver or copper or alloys of gold, silver or copper, as for example brass, (bronze, manganesecopper or alloys of gold or silver with copper, or-a coherent heat-resistant metal such as iron, copper or alloys such as V2A steel or the like which has been coated with tin, zinc, lead, aluminium or chromium, especially in such a form that the said catalysts exhibit more or less coherent surfaces.
- heavy metals of group 1 of the periodic system namely gold, silver or copper or alloys of gold, silver or copper, as for example brass, (bronze, manganesecopper or alloys of gold or silver with copper, or-a coherent heat-resistant metal such as iron, copper or alloys such as V2A steel or the like which has been coated with
- the said metallic coatings are preferably is embedded in metal powder.
- the said metallic materials can also be employed in .a very advantageous mannerfor the thermal conversion of gaseous or vaporous hydrocarbons of the methane series and more particularly the homologues of methane into other hydrocarbons, especially into oleflnes, such as ethylene, propylene, butylene and the like, or into liquid hydrocarbons, especially liquid aromatic hydrocarbons.
- the said metallic materials are advantageously employed as a constructional material for the apparatus.
- the said con version is carried out in the presence of the above mentioned metallic substances with particular advantage when employing free elementary silicon as a catalyst. Commercial silicon may also be employed. 'So much silicon'should always be present in the catalyst that even if some of it enter into combination, free elementary silicon is always present.
- Metals such as iron or copper may be present in the silicon and it may be employed on non-metallic carriers.
- the catalyst is employed in a molded form it is advantageous to prepare it from silicon powder by incorporating therewith non-metallic binding agents such as clay, or other aluminium silicates, or alumina if desired with an addition of metals.
- non-metallic binding agents such as clay, or other aluminium silicates, or alumina if desired with an addition of metals.
- the temperatures required example is converted at lower temperatures than methane.
- a gas containing large amounts of hydrocarbons requires lower temperatures than a gas containing only small amounts thereof.
- reaction products may be very considerably influenced by the temperature and the duration of the treatment.
- a relatively high temperature for example of .more than 700 C. and a short period of heating
- the gaseous initial hydrocarbons are converted into liquid hydrocarbons under nor- 1 mal conditions of temperature and pressure.
- These products consist mainly of aromatic and gasoline-like products and they boil mainly below 200 C. They are admirably suited for employment as non-knocking motor fuels or as 1141- 9 temperatures of between 500 and 700 C. and a 700 C. for a length of centimetres.
- Example 1 l0 litres of a gas having the compositlon 6.16
- Example 3 C. for 60 centimetres o; its length.
- the hydrocarbons employed are converted, so that (calculated with Example 4 8 litres of a gas mixture containing sulphur compounds and consisting 01' about '76 per cent by volume of the methane homologues, ethane,
- propane and butane, 10 per cent of methane, 4 per cent of hydrogen, 8 to 9 per-cent of nitrogen and about 1 to 2 percent of hydrogen sulphide-"ls passed hourly. through a tube having an internal diameter of 20 millimetres and heated over a length of 60 centimetres to a temperature of about 800 C.
- liquid products About 67.2 homologues are converted into liquid products,,30 per cent by weight into methane and 2.5 to 2.8- per cent by weight into gaseous oleflnes. About '10 per cent by weight oi! the liquid hydrocarbons obtained boil at a temperature up to 200 C.
- These 12 consist to the extent 0t 60 to '70 percent of arcmatic hydrocarbons or low boiling point, such as benzene, toluene and xylene, to the extent 01 2 to v 5 per cent of styrene and the remainder of allphatic hydrocarbons o1 low boiling point.
- the liquid products of higher boiling point consist almost exclusively of unsaturated hydrocarbons which are very well suited for. the production 01 lubricating oils of high viscosity.
- the low boiling reaction products are good'motor i'uelsr What we claim is:.
- a process for the production of oleflnes which comprises passing a gas comprising butane, propane and ethane through an internally tinned manganese-copper tube, which is heated to about 700 C.
- a process for the conversion of an impure hydrocarbon of the methane series containing sulphur into more valuable hydrocarbons which comprises treating said hydrocarbon of the meth- 4 ane series at a temperature between 360 and 900 C. and in. the presence of a heatresistant heavy metal of group l of the periodic'system and 01' free elementary silicon.
- a process for the conversion or an impure hydrocarbon of the methane series containing sulphur into more valuable hydrocarbons which comprises treating said hydrocarbon of the methane series at a temperature between 360 and 900 C. and in the presence or an alloy of a heat-* per cent by weight'of the methane ill resistant heavy metal 01' group 1 of the periodic 900 C. and in the presence of a heat resistant system and of free elementary silicon.
- a process for the conversion of an impure hydrocarbon of the methane series containing sulphur into more valuable hydrocarbons which comprises treating said hydrocarbon of the methane series at a temperature between 360 and CERTIFICATE i CORRECTION.
- Patent No. l, 945, 960 Patent No. l, 945, 960.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Patented Feb. 6, 1934 OFFICE 1,945,960 raonuo'non or nrnnocaanons Fritz Winkier and Hans liaeuber, Ludwigshafenon-the-lthine, Germany No Drawing. Application February is, 1931', Serial No. 516,829, and in Germany February 4 Claims.
This invention relates to improvements in the utacture and production of hydrocarbons from gaseous or vaporous hydrocarbons of the methane series.
Unsaturated hydrocarbons, such as ethylene, propylene and the like, may be readily converted into valuable liquid hydrocarbons, such as benzone and benzine, without any injurious deposition of carbon by employing as catalysts heavy metals of group 1 of the periodic system, namely gold, silver or copper or alloys of gold, silver or copper, as for example brass, (bronze, manganesecopper or alloys of gold or silver with copper, or-a coherent heat-resistant metal such as iron, copper or alloys such as V2A steel or the like which has been coated with tin, zinc, lead, aluminium or chromium, especially in such a form that the said catalysts exhibit more or less coherent surfaces.
The said metallic coatings are preferably is embedded in metal powder.
In this manner between the surfaces of the coating metal and of the metal to be coated an alloy of the two metals is usually formed.
We have now found that the said metallic materials can also be employed in .a very advantageous mannerfor the thermal conversion of gaseous or vaporous hydrocarbons of the methane series and more particularly the homologues of methane into other hydrocarbons, especially into oleflnes, such as ethylene, propylene, butylene and the like, or into liquid hydrocarbons, especially liquid aromatic hydrocarbons. The said metallic materials are advantageously employed as a constructional material for the apparatus. The said con version is carried out in the presence of the above mentioned metallic substances with particular advantage when employing free elementary silicon as a catalyst. Commercial silicon may also be employed. 'So much silicon'should always be present in the catalyst that even if some of it enter into combination, free elementary silicon is always present. Metals such as iron or copper may be present in the silicon and it may be employed on non-metallic carriers.
If the catalyst is employed in a molded form it is advantageous to prepare it from silicon powder by incorporating therewith non-metallic binding agents such as clay, or other aluminium silicates, or alumina if desired with an addition of metals. The temperatures required example, is converted at lower temperatures than methane. A gas containing large amounts of hydrocarbons requires lower temperatures than a gas containing only small amounts thereof.
When working under elevated pressures lower temperatures are necessary than at ordinary pressure. Temperatures ranging between 360 and 900 C.'have proved satisfactory. I
Although generally speaking very high temperatures are necessary for this conversion at which hitherto the danger of deposition of carbon was considerable in many cases, only a .very slight deposition of carbon or none at all takes place on the said materials even when working for long periods of time. Moreover, the said materials promote the conversion catalytically to a very great extent.
In many cases it is sufllcient to construct the walls of the reactionchamber of the said materials. Y
As examples of the hydrocarbons which may be converted in accordance with the present invention may be mentioned methane itself or the homologues thereof, such as ethane, propane and butane. Gas mixtures containing these may also be mentioned such as natural gas, waste gases of the destructive hydrogenation of carbonaceous materials such as tars, mineral oils and the like employed.
It is by no means necessary to purify the 1111- .90
' tial materials from sulphur compounds contained therein, as was necessary when working in the f apparatus hitherto employed, but when treating materials containing sulphur, it is necessary to employ as the metal substratum to which the metallic coating is applied a metal or alloy which is not attacked by sulphur, such as V2A steel or other chromium nickel steels.
The nature of the reaction products may be very considerably influenced by the temperature and the duration of the treatment. Thus by employing a relatively high temperature, for example of .more than 700 C. and a short period of heating, the gaseous initial hydrocarbons are converted into liquid hydrocarbons under nor- 1 mal conditions of temperature and pressure. These products consist mainly of aromatic and gasoline-like products and they boil mainly below 200 C. They are admirably suited for employment as non-knocking motor fuels or as 1141- 9 temperatures of between 500 and 700 C. and a 700 C. for a length of centimetres.
short period of heating are employed highly unsaturated liquid hydrocarbons are produced from vaporized hydrocarbons. These said liquid products are particularly well suited for employment as initial materials in the production-of lubricating oils. d I
The following examples will turther. illustrate the nature of this invention, but the invention is not restricted to these examples. The percentmixture at about 1200 C. By a single passage of the gases 90 per cent by weight of the methane 'homologues contained inthe initial gases are ages are by volume. unless otherwise stated.
Example 1 l0 litres of a gas having the compositlon 6.16
per cent by volume of butylene, 37.84 per cent.
by volume of butane, 4.5 per cent by volume of propylene, 39.5 per cent by volume of propane, 0.84 per cent by volume of ethylene and 11.16 per cent by volume of ethane are passed per hour at ordinary pressure through a copper tube 18 millimetres in internal diameter and 60 centimetres in length heated to 800 C. 18 litres of a gas containing 4.0 per cent by volume of hutylenes and propylenes and 31.0'per cent oi. ethylene are obtained perhour. Furthermore, 130 cubic centimetres of liquid hydrocarbons, which consist mainly of benzene, are obtained per cubic metre oi the gas mixture employed. After working for several days the copper tube is still entirely free from carbon. At higher temperatures the yield of) liquid hydrocarbons, especially of benzene, is still higher, and naphthalene and anthracene are also formed.
",Erample 2 4.8 lltres oia gas mixture containing 32.5 per cent of butane, 34 per cent of propane, 9.5 per cent of ethane, 8.4 per cent of higher olefines,
. 0.8 per cent of ethylene and 14.8 per cent of nitrogen are passed per hour through an internally tinned manganese copper tube 18 millimetres ininternal diameter which is heated to After passing thesaid mixture through once a mixture of hydrocarbons, containing 60 per cent by volumeoi oleflnes which in turn contain 67 per cent of ethylene, is obtained. Deposits of car- I bon cannot be detected'atter working for several days.
Example 3 C. for 60 centimetres o; its length. By one pas-' sage 94 per cent by-weight oi the hydrocarbons employed are converted, so that (calculated with Example 4 8 litres of a gas mixture containing sulphur compounds and consisting 01' about '76 per cent by volume of the methane homologues, ethane,
propane and butane, 10 per cent of methane, 4 per cent of hydrogen, 8 to 9 per-cent of nitrogen and about 1 to 2 percent of hydrogen sulphide-"ls passed hourly. through a tube having an internal diameter of 20 millimetres and heated over a length of 60 centimetres to a temperature of about 800 C. The said tube is made of V2A steel and is provided internally with a homogeneous coating of'lead. It is filled with uniform spherold lumps of about the size of peas prepared from silicon powder by molding with a binding agent such as clay and heating the converted. Reckoned on the total initial gases. 25 per cent by weight are converted into ethylene and 30 per centby weight into liquid prod ucts boiling above 40 C. "and consisting of -a1i= phatic and aromatic hydrocarbons: Carbon is 05.
notdeposited in the tube. I
' Example 5 2 cubic metres oi'a gas consisting of 11.5 per cent by weight of 'olefines. 6.5 per cent by weight 100.
of-methane, 81.8 per cent by weight of methane homologues and about 0.2 per cent by weight of hydrogen sulphide are passed under a pressure of 50 atmospheres'through'a tube 5 metres'long-L "same direction as the direction of flow-of the gases.
About 67.2 homologues are converted into liquid products,,30 per cent by weight into methane and 2.5 to 2.8- per cent by weight into gaseous oleflnes. About '10 per cent by weight oi! the liquid hydrocarbons obtained boil at a temperature up to 200 C. These 12 consist to the extent 0t 60 to '70 percent of arcmatic hydrocarbons or low boiling point, such as benzene, toluene and xylene, to the extent 01 2 to v 5 per cent of styrene and the remainder of allphatic hydrocarbons o1 low boiling point. The liquid products of higher boiling point consist almost exclusively of unsaturated hydrocarbons which are very well suited for. the production 01 lubricating oils of high viscosity. The low boiling reaction products are good'motor i'uelsr What we claim is:.
1. A process for the production of oleflnes, which comprises passing a gas comprising butane, propane and ethane through an internally tinned manganese-copper tube, which is heated to about 700 C. I
2. A process for the conversion of an impure hydrocarbon of the methane series containing sulphur into more valuable hydrocarbons, which comprises treating said hydrocarbon of the meth- 4 ane series at a temperature between 360 and 900 C. and in. the presence of a heatresistant heavy metal of group l of the periodic'system and 01' free elementary silicon.
3. A process for the conversion or an impure hydrocarbon of the methane series containing sulphur into more valuable hydrocarbons, which comprises treating said hydrocarbon of the methane series at a temperature between 360 and 900 C. and in the presence or an alloy of a heat-* per cent by weight'of the methane ill resistant heavy metal 01' group 1 of the periodic 900 C. and in the presence of a heat resistant system and of free elementary silicon.
4. A process for the conversion of an impure hydrocarbon of the methane series containing sulphur into more valuable hydrocarbons, which comprises treating said hydrocarbon of the methane series at a temperature between 360 and CERTIFICATE i CORRECTION.
Patent No. l, 945, 960.
February 6, 1934.
FRITZ WINKLER, AL.
It is hereby certified that the above numbered patent was erroneously issued to the inventors said "Winkler-andHaeuber" whereas. said Letters Patent should have been issued to I. G. Farbenindustrie Aktiengesellschaft, Frankfort-on-the-Main, Germany, as assignee ofthe entire interest in said invention, as shown by the records of assignments in this office; and that the said Letters Patent should be read with this correction therein that the same may conform to the record of the case in the Patent Office.
Signed and sealed this 3rd day of April, A. D. 1934.
(Seal) F. M. Hopkins Acting Commissioner of Patents.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1945960X | 1930-02-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1945960A true US1945960A (en) | 1934-02-06 |
Family
ID=7750733
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US516829A Expired - Lifetime US1945960A (en) | 1930-02-20 | 1931-02-18 | Production of hydrocarbons |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1945960A (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1064496B (en) * | 1956-03-07 | 1959-09-03 | Bayer Ag | Process for the dehydrogenation of hydrocarbons |
| US3223743A (en) * | 1961-12-29 | 1965-12-14 | Monsanto Chemicals | Dehydrogenation of ethylbenzene |
| US3244760A (en) * | 1962-11-19 | 1966-04-05 | Dow Chemical Co | Method for cracking aliphatic hydrocarbons |
| US3247276A (en) * | 1962-07-09 | 1966-04-19 | Texaco Inc | Catalytic treatment of hydrocarbons |
| US4507517A (en) * | 1983-10-31 | 1985-03-26 | Chevron Research Company | Conversions of low molecular weight hydrocarbons to higher molecular weight hydrocarbons using a boron compound containing catalyst |
| US4567311A (en) * | 1983-10-31 | 1986-01-28 | Chevron Research Company | Conversions of low molecular weight hydrocarbons to higher molecular weight hydrocarbons using a silicon compound-containing catalyst |
| US4599474A (en) * | 1983-10-31 | 1986-07-08 | Chevron Research Company | Conversions of low molecular weight hydrocarbons to higher molecular weight hydrocarbons using a metal-containing catalyst |
| US4822944A (en) * | 1986-07-11 | 1989-04-18 | The Standard Oil Company | Energy efficient process for upgrading light hydrocarbons and novel oxidative coupling catalysts |
| US4929789A (en) * | 1988-01-15 | 1990-05-29 | The Standard Oil Company | Process for pyrolyzing or thermal cracking a gaseous or vaporized hydrocarbon feedstock using a novel gas-solids contacting device and an oxidation catalyst |
| US5012028A (en) * | 1986-07-11 | 1991-04-30 | The Standard Oil Company | Process for upgrading light hydrocarbons using oxidative coupling and pyrolysis |
| US5066629A (en) * | 1989-06-30 | 1991-11-19 | The Broken Hill Proprietary Company Limited | Oxidative coupling catalyst for methane |
-
1931
- 1931-02-18 US US516829A patent/US1945960A/en not_active Expired - Lifetime
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1064496B (en) * | 1956-03-07 | 1959-09-03 | Bayer Ag | Process for the dehydrogenation of hydrocarbons |
| US3223743A (en) * | 1961-12-29 | 1965-12-14 | Monsanto Chemicals | Dehydrogenation of ethylbenzene |
| US3247276A (en) * | 1962-07-09 | 1966-04-19 | Texaco Inc | Catalytic treatment of hydrocarbons |
| US3244760A (en) * | 1962-11-19 | 1966-04-05 | Dow Chemical Co | Method for cracking aliphatic hydrocarbons |
| US4507517A (en) * | 1983-10-31 | 1985-03-26 | Chevron Research Company | Conversions of low molecular weight hydrocarbons to higher molecular weight hydrocarbons using a boron compound containing catalyst |
| US4567311A (en) * | 1983-10-31 | 1986-01-28 | Chevron Research Company | Conversions of low molecular weight hydrocarbons to higher molecular weight hydrocarbons using a silicon compound-containing catalyst |
| US4599474A (en) * | 1983-10-31 | 1986-07-08 | Chevron Research Company | Conversions of low molecular weight hydrocarbons to higher molecular weight hydrocarbons using a metal-containing catalyst |
| US4822944A (en) * | 1986-07-11 | 1989-04-18 | The Standard Oil Company | Energy efficient process for upgrading light hydrocarbons and novel oxidative coupling catalysts |
| US5012028A (en) * | 1986-07-11 | 1991-04-30 | The Standard Oil Company | Process for upgrading light hydrocarbons using oxidative coupling and pyrolysis |
| US4929789A (en) * | 1988-01-15 | 1990-05-29 | The Standard Oil Company | Process for pyrolyzing or thermal cracking a gaseous or vaporized hydrocarbon feedstock using a novel gas-solids contacting device and an oxidation catalyst |
| US5066629A (en) * | 1989-06-30 | 1991-11-19 | The Broken Hill Proprietary Company Limited | Oxidative coupling catalyst for methane |
| US5132481A (en) * | 1989-06-30 | 1992-07-21 | The Broken Hill Proprietary Company Limited | Process of methane oxidative coupling with hydrogen activation of catalyst |
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