US2266848A - Method of processing hydrocarbons to produce motor fuel - Google Patents
Method of processing hydrocarbons to produce motor fuel Download PDFInfo
- Publication number
- US2266848A US2266848A US193959A US19395938A US2266848A US 2266848 A US2266848 A US 2266848A US 193959 A US193959 A US 193959A US 19395938 A US19395938 A US 19395938A US 2266848 A US2266848 A US 2266848A
- Authority
- US
- United States
- Prior art keywords
- motor fuel
- hydrocarbons
- acetylene
- iso
- produce
- 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
Links
- 239000000446 fuel Substances 0.000 title description 16
- 238000000034 method Methods 0.000 title description 16
- 229930195733 hydrocarbon Natural products 0.000 title description 14
- 150000002430 hydrocarbons Chemical class 0.000 title description 14
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 13
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 11
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 11
- GXDHCNNESPLIKD-UHFFFAOYSA-N 2-methylhexane Natural products CCCCC(C)C GXDHCNNESPLIKD-UHFFFAOYSA-N 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 5
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 5
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- ZUBZATZOEPUUQF-UHFFFAOYSA-N isononane Chemical compound CCCCCCC(C)C ZUBZATZOEPUUQF-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229910044991 metal oxide Inorganic materials 0.000 description 3
- 150000004706 metal oxides Chemical class 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 230000000379 polymerizing effect Effects 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 229930195734 saturated hydrocarbon Natural products 0.000 description 3
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010960 commercial process Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- QAEHINNPWOBLRK-UHFFFAOYSA-N hexane 2-methylhexane Chemical compound CCCCCC.CCCCC(C)C QAEHINNPWOBLRK-UHFFFAOYSA-N 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- -1 methane Chemical class 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000000126 substance 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
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/54—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
- C07C2/56—Addition to acyclic hydrocarbons
- C07C2/58—Catalytic processes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- C07C2523/20—Vanadium, niobium or tantalum
- C07C2523/22—Vanadium
Definitions
- Another object of the invention is to produce pression internal combu ti in 'a motor fuel which may be blended with gaso- Processes of producing branched chain hydroline Stock derived from Crude Petroleum O by carbon motor f l such as isowctane by t distillation or cracking operations, either with catalytic polymerization of butylene and r or without the use of tetraethvl lead, to produce genation of th polymerized product is known in m a motor fuel which will coniorm to all aircraft the art, however commercial processes employfuel spec ficatio s -S' equ y the tradeing mixtures of olefinic gases derived from crack-
- Another object of e invention is t pr du ing butane or other petroleum oils, to product: a hydrocar on mot fu l hav an ta nu i t by known polymerization and ber of at least 100 by the synthetic production drogenating
- a motor fuel may be Another object of the invention is to add hyproduced of any desired number ranging fr m drocarbon radicals to straight chain hydrocar- 90 to 100 or somewhat higher by increasing the bfins iF0 form y c o s With branched chains. number or branch chains of the hydrocarbon 4o Various other jec s a d advanta es of the molecules constituting the fuel. Present i venti Will be pp O the The following representsvgrihically the redescription Of the preferred method Q1 exam..
- C H +H CaH1a iso-octane
- CaH1s+Hz CsH1a iso-octane nadium oxide (V2Oa) or silica.
- the contact mass may be any out the known substances which present large surface exposures. for the space employed, such as asbestos, diatomaceous earth,
- a polymerizing unit of any well known type such as those employing a phosphoric acid catalyst and are therein polymerized to form iso-octylene which is thereafter hydrogenated by known processes to produceiso-octane motor fuel with an octane ranging from 90.t0 100.
- Example 2 Isohexane, derived from any source, such as by the known method of polymerizing propylene to form dimers and thereafter hydrogenating the polymerized product to form the isohexane, is
- the motor fuel thus produced will have an octane 'numher of 90 to 100.
- methane may be processed with acetylene to produce propylene, the propylene polymerized and then hydrogenated to form isohexane, which may be again treated with acetylenein accordance with Example 2 to produce iso-octane with two side chain radicals or groups and an octane value of 98 to 100.
- Process of producing iso-paraffinic hydrocarbons boiling in the usual range of motor fuels which comprises reacting a parafiinic hydrocarbon containing at least three carbon atoms per molecule with acetylene in the presence of a metal oxide catalyst at a temperature of about 350 to 400 F. and hydrogenating the resulting product.
- Process of producing branched chain high antiknock paraffinic motor fuel hydrocarbons which comprises reacting a paraflinic hydrocarbon containing more than two, but less than eight carbon atoms per molecule with acetylene, in the presence of a metal oxide catalyst, at a temperature of about 350 to 400 F., and hydrogenating the resulting product.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
I Patented Dec.23, 1941 2,266,848
UNITED STATES PATENT OFFICE METHOD OF PROCESSING HYDROCARBONS TO PRODUCE MOTOR FUEL Marvin L. Chappell, Berkeley, Calif., assignor of gmlai-fhalf to James W. Weir, Los Angeles, a
No Drawing. Application March 4, 1938,
Serial No. 193,959 Claims. (Cl. 260-676) This invention relates to an improved method In processing hydrocarbons such as isoheptane of P sing hydrocarbons such as methane, the following represents the reaction which takes a e. p op u D hexane, place to produce isononane which may be reguother saturated aliphatic hydrocarbons, to prolated sothat the resultant motor fuel may have duce m r f el with hi h an i-d tona ine har- 5 an octane number greater than 100 in case the aeteristics, a d O W ch m y be ed isoheptane reacted upon by the acetylene gas blended with the various grades of gasoline stock contain 2 or more branched chains. zgeigzgrove the ant1-detonat1ng characteristics CFIHXE+C2H2=C9H18 isononylene Briefly stated, my invention comprises con- C9H18+H2=C9H2 isononane vertirig saturated hydrocarbons into olefines by Isoheptane having two branched chains may be reacting on saturated hydrocarbons with acety produced by reacting on propane with acetylene lene gas, polymerizing the olefines formed and and hydrogenating the resultant product as folhydrogenating the polymerized product to prolows: v duce motor fuel consisting principally of hydrol5 carbons with branched chain molecular struc- C3H8+C2Hi c5H1? lsopentylene a CsH1n+H2-CsH1z lsopentane tures, and/or reacting .on branched chain hy- C5H12+CzH2-C7H14 isoheptylene drocarbons, such as isobutane, isopentane, 1so- C7H14+H2 C7H16 isoheptane hexane, isoheptane, or other isomeric saturated hydrocarbons, with acetylene to produce olefinic An oblect Of t e lnveh'tlon 15 to Produce motor h dr b t an increased number of fuel from saturated straight chain hydrocarbons,
branched chains, and th h d ti the suitable for use in. high compression internal olefinic hydrocarbons to produce saturated hycombustion e s hout the use Of ant drocarbons with nincreased number of knock compounds, such as tetraethyl lead. branched chains it bl as fuel for high Conn Another object of the invention is to produce pression internal combu ti in 'a motor fuel which may be blended with gaso- Processes of producing branched chain hydroline Stock derived from Crude Petroleum O by carbon motor f l such as isowctane by t distillation or cracking operations, either with catalytic polymerization of butylene and r or without the use of tetraethvl lead, to produce genation of th polymerized product is known in m a motor fuel which will coniorm to all aircraft the art, however commercial processes employfuel spec ficatio s -S' equ y the tradeing mixtures of olefinic gases derived from crack- Another object of e invention is t pr du ing butane or other petroleum oils, to product: a hydrocar on mot fu l hav an ta nu i t by known polymerization and ber of at least 100 by the synthetic production drogenating th usually produces motor of hydrocarbons having more than two branched fuel ranging from 90 to 95 octane number, while Chains in the ecular construction. by my improved 'method a motor fuel may be Another object of the invention is to add hyproduced of any desired number ranging fr m drocarbon radicals to straight chain hydrocar- 90 to 100 or somewhat higher by increasing the bfins iF0 form y c o s With branched chains. number or branch chains of the hydrocarbon 4o Various other jec s a d advanta es of the molecules constituting the fuel. Present i venti Will be pp O the The following representsvgrihically the redescription Of the preferred method Q1 exam.. actions which take place in pr essing methane ples of the P o ss mbo y g the p e t and ethane with acetylene for the production ventionof iso-octane. Example 1 For methane-- One volume of ethane derived from any avail- Ch4+c2H2=C3H6 propylene able source is mixed with two volumes of a 2 C3HG p01ymerized=C H isohexylene mixture 0f acetylene and nitrogen gas. This c =c6H14 isohexane r mixture maintained at atmospheric or 1ess than c +c iso-octylene atmospheric pressure is heated to 350-400 F. by C H +H =CaH1a iso-octane any suitable heating means, such as a pipe coil For ethaneheater, and passed therefrom in a continuous CzHs+ChHz=C4H8 butylene I stream flow through a contact mass coated with 2 C4Ha polymerized=CsH1e iso-octylene a catalytic agent such as titanium oxide, va-
CaH1s+Hz=CsH1a iso-octane nadium oxide (V2Oa) or silica. The contact mass may be any out the known substances which present large surface exposures. for the space employed, such as asbestos, diatomaceous earth,
' special constructed porcelain balls or cones, fused magnesium sulphate, slag sand, silica quartz or brick work, and the ilke.
and other gases are conducted to a polymerizing unit of any well known type such as those employing a phosphoric acid catalyst and are therein polymerized to form iso-octylene which is thereafter hydrogenated by known processes to produceiso-octane motor fuel with an octane ranging from 90.t0 100.
Example 2 Isohexane, derived from any source, such as by the known method of polymerizing propylene to form dimers and thereafter hydrogenating the polymerized product to form the isohexane, is
processed with acetylene in accordance with the method described in Example 1, using the same proportional mixture at the same temperature,-
and thereafter hydrogenated by known methods to form iso-octane with two side chains. The motor fuel thus produced will have an octane 'numher of 90 to 100.
By this invention and by the method described in Example 1 methane may be processed with acetylene to produce propylene, the propylene polymerized and then hydrogenated to form isohexane, which may be again treated with acetylenein accordance with Example 2 to produce iso-octane with two side chain radicals or groups and an octane value of 98 to 100.
While the process herein described is well adapted for carrying out the objects of the present invention various forms and modifications may be made, such for example as the use of various forms of reaction chambers employing various forms of heat exchangers to extract the exothermic heat of the acetylization reaction, and the invention includes all such modifications and changes as appear in the scope of the appended claims.
Iclaim:
1. In a process of producing a branched chain high anti-knock paraffinic motor fuel hydrocarbon, the step which comprises reacting acetylene with an isohexane.
2. Process of producing iso-paraffinic hydrocarbons boiling in the usual range of motor fuels, which comprises reacting a parafiinic hydrocarbon containing at least three carbon atoms per molecule with acetylene in the presence of a metal oxide catalyst at a temperature of about 350 to 400 F. and hydrogenating the resulting product.
3. Process of producing branched chain high antiknock paraffinic motor fuel hydrocarbons, which comprises reacting a paraflinic hydrocarbon containing more than two, but less than eight carbon atoms per molecule with acetylene, in the presence of a metal oxide catalyst, at a temperature of about 350 to 400 F., and hydrogenating the resulting product.
4. Process of increasing the number of branched chains in iso-paraflinic hydrocarbons,
and thereby increasing their antiknock value,
which comprises reacting iso-paraifins containing less than eight carbon atoms per molecule, with acetylene, in the presence of a metal oxide ca'tproduct.
MARVIN L. CHAPPELL.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US193959A US2266848A (en) | 1938-03-04 | 1938-03-04 | Method of processing hydrocarbons to produce motor fuel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US193959A US2266848A (en) | 1938-03-04 | 1938-03-04 | Method of processing hydrocarbons to produce motor fuel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2266848A true US2266848A (en) | 1941-12-23 |
Family
ID=22715740
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US193959A Expired - Lifetime US2266848A (en) | 1938-03-04 | 1938-03-04 | Method of processing hydrocarbons to produce motor fuel |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2266848A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3125498A (en) * | 1964-03-17 | Method of upgrading light | ||
| US3211635A (en) * | 1961-04-14 | 1965-10-12 | Phillips Petroleum Co | Production of olefins from paraffins and acetylenes |
| 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 |
-
1938
- 1938-03-04 US US193959A patent/US2266848A/en not_active Expired - Lifetime
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3125498A (en) * | 1964-03-17 | Method of upgrading light | ||
| US3211635A (en) * | 1961-04-14 | 1965-10-12 | Phillips Petroleum Co | Production of olefins from paraffins and acetylenes |
| 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 |
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