US2403524A - Process for the preparation of highgrade antiknock motor fuels - Google Patents
Process for the preparation of highgrade antiknock motor fuels Download PDFInfo
- Publication number
- US2403524A US2403524A US382639A US38263941A US2403524A US 2403524 A US2403524 A US 2403524A US 382639 A US382639 A US 382639A US 38263941 A US38263941 A US 38263941A US 2403524 A US2403524 A US 2403524A
- Authority
- US
- United States
- Prior art keywords
- hydrocarbons
- treatment
- preparation
- motor fuels
- highgrade
- 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
- 238000000034 method Methods 0.000 title description 12
- 239000000446 fuel Substances 0.000 title description 10
- 238000002360 preparation method Methods 0.000 title description 3
- 150000001336 alkenes Chemical class 0.000 description 10
- 229930195733 hydrocarbon Natural products 0.000 description 10
- 150000002430 hydrocarbons Chemical class 0.000 description 10
- 150000001298 alcohols Chemical class 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 7
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 229910002091 carbon monoxide Inorganic materials 0.000 description 6
- 239000003502 gasoline Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 238000005984 hydrogenation reaction Methods 0.000 description 5
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 5
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 5
- 238000005336 cracking Methods 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000004523 catalytic cracking Methods 0.000 description 3
- 229910000286 fullers earth Inorganic materials 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000009835 boiling Methods 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- ONRNGLBTDCWMAM-UHFFFAOYSA-N BOP(O)(O)=O Chemical compound BOP(O)(O)=O ONRNGLBTDCWMAM-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-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
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/16—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxo-reaction combined with reduction
-
- 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
- Y10S585/93—Process including synthesis of nonhydrocarbon intermediate
- Y10S585/934—Chalcogen-containing
Definitions
- Unsaturated low molecular hydrocarbons such as are obtained for example in the catalytic cracking of high molecular hydrocarbons, can be converted by prior art methods into highly anti- However, in hydrogenating these polymerizates, which is absolutely necessary for producing motor fuels suitable for aircraft purposes, the anti-knock property of the gasolin is greatly decreased.
- the object of the present invention is to convert these hydrocarbons, especially those with from 3 to 5 carbon atoms, into a product which, even after hydrogenation, has excellent antiknock properties.
- the low molecular hydrocarbons are treated with carbon monoxide and hydrogen at high pressures of about 50-200 atmospheres, and temperatures of up to, and if necessary above, 300 C. (572 F.). Alcohol are thus formed, which are converted at normal pressure into alkenes having branched chains, by the usual process of heating with dehydrating means, such as alumina. Subsequently, a hydrogenation is conducted. If desired, the treatment with carbon monoxide and hydrogen may be repeatedly carried out with the alkenes obtained, until the hydrogenated final products have the boiling points required for application as aircraft gasoline.
- the starting material with borylphosphate, fullers earth or similar substances at a high temperature, for example at 200-300 C. (392-5'72 F.), partly in order to isomerize the unsaturated hydrocarbons, and partly to shift the double bond towards the middle of the molecule, which is very favourable for the addition of branched-chain methyl groups through the watergas treatment.
- the final hydrogenation can be preceded by another treatment with agencies such as borylphosphate, fullers earth, etc.
- a very favourable mode of execution of the above described process results if the products obtained after the dehydrating step are separated into three fractions, a low-molecular fraction, a high-molecular fraction within the gasoline boiling range, and a medium-molecular fraction.
- the low molecular hydrocarbons are then recycled and subjected to the treatment with isomerizing means'which precedes the watergas treatment, while the medium molecular hydrocarbons are recycled to the watergas treatment used for the preparation of alcohols, if desired after the treatment with borylphosphate, etc.
- the higher molecular fractions, if desired after further treatment with borylphosphate etc. are immediately subjected to hydrogenation. In this way, for example, it is possible to effect a thoroughly satisfactory conversion of the C3- to cs-hydrocarbons, obtained in large quantities by the catalytic cracking, into Valuable aircraft gasoline.
- the process of making high-grade antiknock motor fuels which comprises treating the unsaturated hydrocarbons, derived from the cracking of high molecular hydrocarbons and having from about 3 to 5 carbon atoms in the molecule, to a selective polymerization of the unsaturated iso-hydrocarbons present, treating the resulting products with carbon monoxide and hydrogen at temperatures of at least about 300 C. under conditions producing the conversion of the alkenes present into alcohols, subjecting these alcohols to a dehydrating step under conditions producing the formation of alkenes and hydrogenating the resulting alkenes, thereby producing an aircraft fuel having a remarkably high octane number.
- the process of making high-grade anti- -kno'ck fue1s which comprises treating the unsaturated hydrocarbons, having from 3 to 5 carbon atoms derived from the cracking of high molecular hydrocarbons, to isomerize them and to shift the double bonds towards the centers of the molecules "by contacting them with a catalyst :selected from a class-consisting of borylphosphate 4 and fullers earth at a temperature ranging from about 200 C. to 300 C. and then heating the resulting product with carbon monoxide and hydrogen under high pressures and at temperatures of at least about 300 C.
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
.knock gasoline polymerizates.
Patented July 9, 1946 PROCESS FOR THE PREPARATION OF HIGH- GRADE ANTIKNOCK MOTOR FUELS August Hagemann,
Duisburg-Meiderich, Germany; vested in the Alien Property Custodian No Drawing. Application March 10, 1941, Serial No. 382,639. In Germany February 8, 1940 6 Claims. 1
Unsaturated low molecular hydrocarbons, such as are obtained for example in the catalytic cracking of high molecular hydrocarbons, can be converted by prior art methods into highly anti- However, in hydrogenating these polymerizates, which is absolutely necessary for producing motor fuels suitable for aircraft purposes, the anti-knock property of the gasolin is greatly decreased.
The object of the present invention is to convert these hydrocarbons, especially those with from 3 to 5 carbon atoms, into a product which, even after hydrogenation, has excellent antiknock properties. To obtain this result, the low molecular hydrocarbons are treated with carbon monoxide and hydrogen at high pressures of about 50-200 atmospheres, and temperatures of up to, and if necessary above, 300 C. (572 F.). Alcohol are thus formed, which are converted at normal pressure into alkenes having branched chains, by the usual process of heating with dehydrating means, such as alumina. Subsequently, a hydrogenation is conducted. If desired, the treatment with carbon monoxide and hydrogen may be repeatedly carried out with the alkenes obtained, until the hydrogenated final products have the boiling points required for application as aircraft gasoline.
Before the watergas treatment it is advisable to introduce a selective polymerization step, whereby only the iso-hydrocarbons are polymerized. Then, by the addition of a methyl group through the watergas treatment, the polymerizates obtained yield compounds which, as regards their anti-knock property, even surpass isooctane.
Furthermore, before the watergas treatment, it is advisable to treat the starting material with borylphosphate, fullers earth or similar substances at a high temperature, for example at 200-300 C. (392-5'72 F.), partly in order to isomerize the unsaturated hydrocarbons, and partly to shift the double bond towards the middle of the molecule, which is very favourable for the addition of branched-chain methyl groups through the watergas treatment. In the same Way, the final hydrogenation can be preceded by another treatment with agencies such as borylphosphate, fullers earth, etc.
A very favourable mode of execution of the above described process results if the products obtained after the dehydrating step are separated into three fractions, a low-molecular fraction, a high-molecular fraction within the gasoline boiling range, and a medium-molecular fraction. The low molecular hydrocarbons are then recycled and subjected to the treatment with isomerizing means'which precedes the watergas treatment, while the medium molecular hydrocarbons are recycled to the watergas treatment used for the preparation of alcohols, if desired after the treatment with borylphosphate, etc. On the other hand, the higher molecular fractions, if desired after further treatment with borylphosphate etc., are immediately subjected to hydrogenation. In this way, for example, it is possible to effect a thoroughly satisfactory conversion of the C3- to cs-hydrocarbons, obtained in large quantities by the catalytic cracking, into Valuable aircraft gasoline.
If desired, one can add to the aircraft gasoline the saturated Cs-hydrocarbons, which during the Watergas treatment pass off with the saturated Csand C i-hydrocarbons that escape as gases, while the latter may be used as fuel gas.
The process described permits a practically complete conversion of the C3- to cs-hydrocarbons, especially obtained in large quantities by the catalytic cracking, into an aircraft gasoline with a remarkably high octane number. In this connection it should be observed that this conversion can be effected by comparatively simple means.
What I claim is:
1. The process of making high-grade antiknock motor fuels which comprises treating the unsaturated hydrocarbons, derived from the cracking of high molecular hydrocarbons and having from about 3 to 5 carbon atoms in the molecule, to a selective polymerization of the unsaturated iso-hydrocarbons present, treating the resulting products with carbon monoxide and hydrogen at temperatures of at least about 300 C. under conditions producing the conversion of the alkenes present into alcohols, subjecting these alcohols to a dehydrating step under conditions producing the formation of alkenes and hydrogenating the resulting alkenes, thereby producing an aircraft fuel having a remarkably high octane number.
2. The process of claim 1 wherein the products obtained after the dehydrating step are separated into a high molecular fraction, a low molecular fraction and a medium fraction, the high molecular fraction being subjected directly to the hydrogenating step, the low molecular fraction being recycled to the selective polymerization step, and the medium fraction being recycled to the treatment with carbon monoxide and hydrogen.
3. The process of claim 1 wherein the reaction products are subjected to an isomerizing step after the dehydrating step and before hydrogenation.
4. The process of making high-grade antiknock motor fuels which comprises subjecting the unsaturated hydrocarbons, derived from the cracking of high molecular hydrocarbons and having from about 3 to 5 carbon atoms in the molecule, to the action of a catalyst selected from a class consisting of boryl phosphate and full'ers earth at a temperature ranging from about 200 to 300 0., treating the resulting products with carbon monoiride and hydrogen at a temperature of at least about 300 C. under conditions producing the conversion of the alkenes present into alcohols, subjecting these alcohols .to a dehydrating step, isomerizing the resulting product and then hydrogenating, thereby producing an aircraft fuel having a remarkably high octane num- "her.
'5. The process of making high-grade anti- -kno'ck fue1s which comprises treating the unsaturated hydrocarbons, having from 3 to 5 carbon atoms derived from the cracking of high molecular hydrocarbons, to isomerize them and to shift the double bonds towards the centers of the molecules "by contacting them with a catalyst :selected from a class-consisting of borylphosphate 4 and fullers earth at a temperature ranging from about 200 C. to 300 C. and then heating the resulting product with carbon monoxide and hydrogen under high pressures and at temperatures of at least about 300 C. under conditions producing the conversion of the alkenespresent into alcohols, subjecting these alcohols to;a dehydrat ing step under conditions producing the formation of alkenes and hydrogenating the resulting alkenes, thereby producing an aircraft fuel having a, remarkably high octane number.
'6.'The process of making high-grade antiknock fuels which comprises heating the unsaturated hydrocarbons, haVing from 3 to 5 carbon atoms derived "from the cracking of high molecular hydrocarbons to a selective polymerization of the unsaturated iso-hydrocarbons and then treating the resulting product with carbon monoxide andhyclrogen under high pressures and at temperatures of at leastabout 300 C. under conditions producing the conversion of the alk'enes present into alcohols, subjecting these alcohols to a dehydrating step under conditions producing the formation of alkenes and 'hydrogenating the resulting alkenes, thereby producing an aircraft fuel'having a remarkably high octane number.
AUGUST HAGEMANN.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2403524X | 1940-02-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2403524A true US2403524A (en) | 1946-07-09 |
Family
ID=7995801
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US382639A Expired - Lifetime US2403524A (en) | 1940-02-08 | 1941-03-10 | Process for the preparation of highgrade antiknock motor fuels |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2403524A (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2540587A (en) * | 1946-02-07 | 1951-02-06 | Standard Oil Dev Co | Process for producing hydrocarbons |
| US2549111A (en) * | 1948-05-28 | 1951-04-17 | Texas Co | Combination synthesis of hydrocarbons and organic carbonyl compounds |
| US2554202A (en) * | 1947-10-21 | 1951-05-22 | Ici Ltd | Isomerization of olefins with boron ortho phosphate catalyst |
| US2564130A (en) * | 1948-07-24 | 1951-08-14 | Du Pont | One-step butyl alcohol process |
| US2609397A (en) * | 1948-07-24 | 1952-09-02 | Du Pont | Primary alcohol composition |
| US2623074A (en) * | 1948-08-19 | 1952-12-23 | Standard Oil Dev Co | Production of alcohols and gasoline by the oxo process |
| US2628981A (en) * | 1947-11-29 | 1953-02-17 | Standard Oil Co | Preparation of improved motor fuel |
| US2683177A (en) * | 1949-10-29 | 1954-07-06 | Standard Oil Co | Single stage process for preparing alcohols from co, h2 and olefins |
| US2731503A (en) * | 1951-05-10 | 1956-01-17 | Exxon Research Engineering Co | Alcohol synthesis process |
-
1941
- 1941-03-10 US US382639A patent/US2403524A/en not_active Expired - Lifetime
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2540587A (en) * | 1946-02-07 | 1951-02-06 | Standard Oil Dev Co | Process for producing hydrocarbons |
| US2554202A (en) * | 1947-10-21 | 1951-05-22 | Ici Ltd | Isomerization of olefins with boron ortho phosphate catalyst |
| US2628981A (en) * | 1947-11-29 | 1953-02-17 | Standard Oil Co | Preparation of improved motor fuel |
| US2549111A (en) * | 1948-05-28 | 1951-04-17 | Texas Co | Combination synthesis of hydrocarbons and organic carbonyl compounds |
| US2564130A (en) * | 1948-07-24 | 1951-08-14 | Du Pont | One-step butyl alcohol process |
| US2609397A (en) * | 1948-07-24 | 1952-09-02 | Du Pont | Primary alcohol composition |
| US2623074A (en) * | 1948-08-19 | 1952-12-23 | Standard Oil Dev Co | Production of alcohols and gasoline by the oxo process |
| US2683177A (en) * | 1949-10-29 | 1954-07-06 | Standard Oil Co | Single stage process for preparing alcohols from co, h2 and olefins |
| US2731503A (en) * | 1951-05-10 | 1956-01-17 | Exxon Research Engineering Co | Alcohol synthesis process |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR102589091B1 (en) | Method of manufacturing fuel additives | |
| JPS6158510B2 (en) | ||
| GB1383229A (en) | Production of gaseous olefins from petroleum residue feedstocks | |
| EP3790854B1 (en) | Method of producing a fuel additive | |
| US2403524A (en) | Process for the preparation of highgrade antiknock motor fuels | |
| GB935718A (en) | Catalytic hydrogenative refining of hydrocarbon oils | |
| GB1429331A (en) | Process for the production of synthesis gas and clean fuels | |
| US2367527A (en) | Motor fuel | |
| US2500755A (en) | Polymerization of cycle oil from high-temperature steam cracking process | |
| US2574449A (en) | Process of catalytic desulfurization of naphthenic petroleum hydrocarbons followed by catalytic cracking | |
| US2326166A (en) | Process for the production of nonknocking motor fuels | |
| US2386468A (en) | Process for isomerizing normal butenes to isobutene | |
| US2331930A (en) | Splitting of hydrocarbons | |
| US2935465A (en) | Catalytic conversion of hydrocarbons | |
| US2344789A (en) | Destructive hydrogenation of hydrocarbon oils | |
| US2321841A (en) | Refining hydrocarbons | |
| DE2262607A1 (en) | Pyrolysis of petroleum fractions - under pressure in presence of steam and methane to olefins and aromatics | |
| US2589273A (en) | Process for deoxygenating and isomerizing a fischer-tropsch stock | |
| US1863670A (en) | Production of viscous oils and hydrocarbon products of low boiling point | |
| US2556275A (en) | Process of treating a hydrocarbon synthesis naphtha product | |
| EP3935139B1 (en) | Method of producing a fuel additive | |
| GB1073255A (en) | Process and apparatus for the production of ethylene by pyrolysis of petroleum hydrocarbons | |
| US3340178A (en) | Process for catalytically cracking pyrolysis condensates | |
| SU364656A1 (en) | METHOD OF OBTAINING ETHYLENE | |
| US2116723A (en) | Process for manufacturing hydrocarbon oils |