US2952612A - Production of high octane motor fuel with an alkyl ether additive - Google Patents
Production of high octane motor fuel with an alkyl ether additive Download PDFInfo
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- US2952612A US2952612A US668303A US66830357A US2952612A US 2952612 A US2952612 A US 2952612A US 668303 A US668303 A US 668303A US 66830357 A US66830357 A US 66830357A US 2952612 A US2952612 A US 2952612A
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- 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
- C10G69/00—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process
-
- 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
- C10G69/00—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process
- C10G69/02—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process plural serial stages only
- C10G69/04—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process plural serial stages only including at least one step of catalytic cracking in the absence of hydrogen
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
- C10L1/023—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for spark ignition
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/185—Ethers; Acetals; Ketals; Aldehydes; Ketones
- C10L1/1852—Ethers; Acetals; Ketals; Orthoesters
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- 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
- C10G2400/02—Gasoline
Definitions
- This invention relates to the production of quality automotive motor fuel through catalytic cracking, hydrotreating, and blending.
- the backbone, so to speak, of gasoline for automotive use is catalytically cracked gasoline. It is the practice to charge the maximum amount of suitable oils boiling above gasoline to catalytic cracking to thereby maximize the yield of this material. Due to the excellent quality of catalytically cracked gasoline it is possible to blend with it minor amounts of lower quality materials such as straight run gasoline. In order to maximize the utilization of such low cost materials it is the practice in many instances to add to the blend other high octane materials such, for example, as alkylate, aromatic extracts and catalytically reformed gasoline. Of course, small amounts of butane are incorporated to obtain the desired vapor pressure of the final blend and the gasoline is usually leaded.
- saturated alkyl ethers and particularly those having a branched chain and boiling within the range of about 89 F. to about 180 F.
- Di-isopropyl ether was used to a limited extent during World War II in aviation gasoline. These ethers would be efiective in automotive motor fuel. They are, however, so costly that they have not been used in automotive fuel, or, for that matter, even in aviation gasoline, since the war.
- the transition point where reduction of the bromine number by hydrogenation passes from bad to good is at about 11% ether based on the catalytically cracked gasoline or about 10% in the blend. At this point a small reduction of the bromine number by a very light hydrogenation has no effect; a more drastic reduction in the bromine number is still harmful. At still higher ether concentrations the partial reduction of the bromine number by hydrogenation is advantageous and the advantage increases as the concentration of ether in the'blend is increased. This trend persists at least up to about 44% concentration of the ether beyond which tests were considered to be unwarranted due to the high cost of blends with such high concentrations of ether. At this point (44%) the saving in ether effected through the partial reduction of the bromine number is around 40%, is. the amount of ether required to produce a given volume of a blend having a given octane number is 40% less than would be required without the hydrogenation.
- the concentration has only one meaning.
- the present invention allows a desired octane level to be reached With reduced amounts of ether.
- concentrations above this break point there are therefore two ether concentrations to be considered, namely, (1) the concentration of ether required .to achieve a given octane level without partial reduction of the bromine number of the catalytically cracked gasoline and (2) the concentration of ether required to achieve the same octane level with partial reduction of the bromine number.
- concentration of ether required to achieve the same octane level with partial reduction of the bromine number.
- the figures in the first column of Table II labelled three times the percent ether in the blend. For example in the case of the blend containing 31% ether where a saving of about 28% is indicated at a bromine number reduction of 50%, the saving is still 23% if the bromine number reduction is increased to
- the eifects noted are obtained with cataltyically cracked gasoline produced by the catalytic cracking of any hydrocarbon oil boiling above gasoline with a solid silica-alumina type cracking catalyst. It is known that the silica-alumina cracking catalysts whether of high or low alumina content or of natural or synthetic origin give practically identical gasolines from various oils. Other cracking catalysts such as silica-magnesia and HIE treated alumina give difierent product distributions and the gasolines produced with them may not behave in the manner shown when blended with the ethers.
- the catalytically cracked gasoline is produced by the catalytic cracking of a higher boiling hydrocarbon oil at temperatures in the range of 900 to about 1100 F., pressures in the range of 5 to'about 75'p.s.i.g.
- the cracking may be etfected in a fluid bed reactor, moving bed reactor or a riser reactor such as described in U. S. application Serial Number 586,105, filed May 21, 1956.
- the products from the cracking reactor are preferably separated into a normally gaseous fraction including substantial amounts of olefins, a catalytically cracked gasoline boiling up to about 185-25.0 R, and a heavy naphtha.
- This naphtha fraction is advantageously catalytically reformed and then combined with the blend of the hydrogenated catalytically cracked gasoline and the ether.
- the reforming may be affected by any of the known catalytic reforming processes.
- the naptha is Platformed by a platinum-alumina-halogencatalyst at a temperature of 900-960 F. and pressure of 150-450 p.s.i.g. in the presence of recycled hydrogen.
- the amount of reformed naphtha or other blending materials that may be incorporated to produce the finished gasoline of desired octane number may be increased; such components can in fact become the chief component in the gasoline.
- the advantage can be exploited in a difierent way.
- the naphtha may be used in the same amount but may be reformed to a lesser degree as by the use of less severe reforming conditions, thereby lowering the reforming cost and improving the yield of reformed product.
- the catalytically cracked gasoline is catalytically hydrogenated to reduce the bromine number at least to some degree and preferably to about the extents indicated.
- the bromine number is initially at least around 100.
- the hydrogenation may be effected with any of the various hydrogenation catalysts hitherto used for hydrogenation of petroleum products.
- Preferred catalysts are prepared by incorporating oxides or sulfides of one or more to the metals Ou, Co, Ni, Cr, Mo, W with an aluminous carrier material such asactivated alumina or microporous silica-alumina composites.
- the hydrogenation is efiectd at temperatures in the range of about 300 to 800 F., preferably about 500 to 700 F.
- the process may be carried out under pressures from slightly above atmospheric up to about 100 atmospheres.
- the rate of gasoline and hydrogen feed to the hydrogenation zone may be adjusted such that the desired degree of bromine number reduction is obtained.
- a bromine number reduction of from about 50 to about there is a substantial exothermic heat effect which makes control of the temperature difiicult.
- This difiiculty can be minimized by using two small reactors in series .with'intermediate cooling of the reactant stream, or by adding to the feed a sizable amount of a substantially inert hydrocarbon diluent material having a sufliciently different boiling range that it may be separated from the partially hydrogenated catalytically cracked gasoline product by a subsequent fractional distillation.
- the ether is advantageously made from the olefinic gaseous fraction mentioned above. This is advantageous in two respects. -In the first place this materially upgrades this gaseous product. In the second place the conversion of propylene and/or butylene to ethers reduces the amount of polymers which would otherwise be made fi'om them. This is advantageous since the polymers tend to degrade the quality of the gasoline in which they are blended.
- the conversion of the gaseous olefins to ethers may be efiected by reacting them with a suitable alcohol such as methanol, or isopropanol by known methods e.g., as described in U.S. Patent No. 2,480,940 to Leum.
- a very desirable arrangement which produces large Volumes of the ether is to hydrate the propylene to isopropyl alcohol (a known process) and then react this alcohol with the butylene-butane fraction or additional propylene whereby isopropyl tertiary butyl ether or di-isopropyl ether is formed.
- Still larger volumes of the ether may be produced but at increased cost, by reacting both the propylene and the isobutylene with methanol to produce methyl isopropyl and methyl tertiary butyl ethers.
- the etherification reaction normally does not consume all of the alcohol in the reaction mixture. Unreacted alcohol may be removed by water washing the ether product or in some cases by distillation.
- the ethers in question are normally liquid and are easily separated from the unreacted hydrocarbons (e.g., butane-butylene fractions) by a simple distillation.
- the flashed distillate and deasphalted oil were catalytically cracked together in a commercial fluidized catalyst cracking unit using a synthetic silica-alumina cracking catalyst.
- the product was fractionated in the plant in the normal manner to separate a propane-propylene fraction, a butanebutylene fraction, a catalytically cracked gasoline having the properties given above, and various heavier materials.
- the catalytically cracked gasoline was partially bydrogenated with a commercial Co-Mo/alumina catalyst at 536-608 F. and 200 p.s.i.g. at a hydrogen to oil mole ratio of 2.8 and a liquid hourly space velocity of 4 to reduce the bromine number by 63%,
- isopropyl tertiary butyl ether was found equally effective as the methyl tertiary butyl ether and methyl tertiary amyl ether and ethyl tertiary butyl ether were intermediate the isopropyl tertiary butyl and di-isopropyl ether.
- the F-l-S octane number is the CFR designation for the ASTM Research Octane Number D908-47T for the material containing 3 cc. of ethyl fluid per US, gallon.
- the bromine numbers were determined by the meth od described by A. Polgar et al. in Organic Analysis, vol. III, p. 237, Interscience Publishers, N.Y.
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- Engineering & Computer Science (AREA)
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- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
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- Liquid Carbonaceous Fuels (AREA)
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Description
Sept. 13, 1960 CAI'. CRACKER FEED R. P. TRAINE v PRODUCTION OF HIGH OCTANE MOTOR FUEL WITH 1 AN ALKYL EITHER ADDITIVE Filed June 27; 1957 CATALYTIC CRACKING SILICA- ALUMINA' -'IY'YPE CATALYST l+ FRACTIONATIION NORMALLY GASEOUS FRACTION I END POINT I |80-250F\ TO ETHYER HYI'DROGENATION-TO I PRODUCTION SPECIFIED 7 BR. NO. REDUCTION I 'LAT LEAST 12%v ETHERI MOTOR GASOLINE 1 REFORM I I I I I I I INVENTOR:
RICHARD P. TRAINER S ATTORNEY United States Patent PRODUCTION OF HIGH OCTANE MOTOR FUEL WITH AN ALKYL ETHER ADDITIVE Richard P. Trainer, Pleasant Hill, Calif., assignor to Shell Oil Company, New York, N.Y., a corporation of Delaware Filed June 27, 1957, Ser. No. 668,303
9 Claims. (Cl. 20867) This invention relates to the production of quality automotive motor fuel through catalytic cracking, hydrotreating, and blending.
The backbone, so to speak, of gasoline for automotive use is catalytically cracked gasoline. It is the practice to charge the maximum amount of suitable oils boiling above gasoline to catalytic cracking to thereby maximize the yield of this material. Due to the excellent quality of catalytically cracked gasoline it is possible to blend with it minor amounts of lower quality materials such as straight run gasoline. In order to maximize the utilization of such low cost materials it is the practice in many instances to add to the blend other high octane materials such, for example, as alkylate, aromatic extracts and catalytically reformed gasoline. Of course, small amounts of butane are incorporated to obtain the desired vapor pressure of the final blend and the gasoline is usually leaded.
Among such high octane materials which have been suggested for use in gasolines are the saturated alkyl ethers, and particularly those having a branched chain and boiling within the range of about 89 F. to about 180 F. Di-isopropyl ether was used to a limited extent during World War II in aviation gasoline. These ethers would be efiective in automotive motor fuel. They are, however, so costly that they have not been used in automotive fuel, or, for that matter, even in aviation gasoline, since the war.
It has now been found that the effectiveness of these ethers may be materially improved in combination with catalytically cracked gasoline in automotive fuel, provided the catalytically cracked gasoline is first partially hydrogenated to reduce its bromine number and certain minimum concentrations of ether are used. This finding is considered quite unexpected since blends of the ethers with hydrogenated catalytically cracked gasoline normally have considerably lower octane numbers than the corresponding blends with the non-hydrogenated catalytically cracked gasoline. Another way of putting it is to say that the more the catalytically cracked gasoline is hydrogenated to reduce its bromine number the more of the costly ether is normally required to achieve a given octane number.
This is best illustrated by the data in Table I which show the amounts of methyl tertiary butyl ether that must be added to a 100.9 F-l3 octane number catalytically cracked gasoline unhydrogenated and hydrogenated (to reduce the bromine number to various extents) to produce blends having octane numbers of 100.0, 100.5, 101.0 and 101.5, respectively. The percentages of ether are the concentrations by volume in the blend.
Table I F1-3 Octane Number Bromine No. Reduction, 100.5 101 101.5 percent (by hydrogenation) Percent Ether Required in Blend It is clearly evident that the more the bromine number is reduced by hydrogenation the greater is the concentration of other required to achieve a given octane number. A similar effect is found if the methyl tertiary butyl ether is substituted by other low boiling ether such as methyl isopropyl ether, di-isopropyl ether, ethyl isopropyl ether and isopropyl tertiary butyl ether. It is also found with some of the higher boiling cyclic ethers wherein etheroxygen is in a ring with carbon atoms, such as 4,4-dimethyl-1,3-dioxane.
It is found, however, that at high concentrations of these ethers in the blend with the catalytically cracked gasoline a point is reached where partial reduction of the bromine number of the catalytically cracked gasoline by hydrogenation does not show this advantage but is distinctly advantageous. In this region of high ether concentration partial (25-95%) reduction of the bromine number allows the production of super blends to which larger amounts of other lower octane materials may be added while still producing premium quality automotive fuel.
The transition point where reduction of the bromine number by hydrogenation passes from bad to good is at about 11% ether based on the catalytically cracked gasoline or about 10% in the blend. At this point a small reduction of the bromine number by a very light hydrogenation has no effect; a more drastic reduction in the bromine number is still harmful. At still higher ether concentrations the partial reduction of the bromine number by hydrogenation is advantageous and the advantage increases as the concentration of ether in the'blend is increased. This trend persists at least up to about 44% concentration of the ether beyond which tests were considered to be unwarranted due to the high cost of blends with such high concentrations of ether. At this point (44%) the saving in ether effected through the partial reduction of the bromine number is around 40%, is. the amount of ether required to produce a given volume of a blend having a given octane number is 40% less than would be required without the hydrogenation.
For concentrations of the ether up to the above-mentioned break point the concentration has only one meaning. As already pointed out, however, the present invention allows a desired octane level to be reached With reduced amounts of ether. At concentrations above this break point there are therefore two ether concentrations to be considered, namely, (1) the concentration of ether required .to achieve a given octane level without partial reduction of the bromine number of the catalytically cracked gasoline and (2) the concentration of ether required to achieve the same octane level with partial reduction of the bromine number. For all concentrations beyond the break point it will be understood that the latter concentration is meant. This is the concentration that will be meaningful in the practice of the invention since it is directed to the concentrations that will be used rather than to the concentrations that would otherwise have to be used. For example, in the above-mentioned case of 44% concentration of ether with a saving in ether of about 40%, this mearis-thatiabout 78% of the ether, based on the partially hydrogenated catalytically cracked gasoline, is added to produce a blend containing about 44% ether by volume, whereas about 285% would otherwise have to be added to produce a blend containing about 74% by volume of ether.
The beneficial effect of partial bromine number reduction at high ether concentrations is shown in the following Table II.
. Table 11 Percent Ether by Volume Required for Approxi- Equivalent F-1-3 mate Re- .llydrogenati n-hromme N0. Octan Numbers duction in Reduction Ether Requireruent, Without With I percent Hydro- -Hydrgenation genation The above data are for blends of methyl tertiary butyl ether in the same catalytically cracked gasoline mentioned above in connection with Table I. The partial reduction of the bromine number was effected by partially hydrogenating the catalytically cracked gasoline with a commercial alumina-supported cobalt, molybdenum catalyst at temperatures in the range of 536 to 698 F. and pressures of 200 and 400 p.s.i.g. using 2900 s.c.f-. hydrogen per barrel of gasoline. The catalytically cracked gasoline was obtained from a commercial operation using a synthetic silica-alumina cracking catalyst and before partial hydrogenation had the following prop erties:
Gravity, API 79.1 I.B.P., ASTM, F- 102 F.B.P., ASTM, F 187 Percent S 0.014 Br No a r r 141 F-'-1-3 Octane No 100.9
The figures in the first column of Table II labelled three times the percent ether in the blend. For example in the case of the blend containing 31% ether where a saving of about 28% is indicated at a bromine number reduction of 50%, the saving is still 23% if the bromine number reduction is increased to The eifects noted are obtained with cataltyically cracked gasoline produced by the catalytic cracking of any hydrocarbon oil boiling above gasoline with a solid silica-alumina type cracking catalyst. It is known that the silica-alumina cracking catalysts whether of high or low alumina content or of natural or synthetic origin give practically identical gasolines from various oils. Other cracking catalysts such as silica-magnesia and HIE treated alumina give difierent product distributions and the gasolines produced with them may not behave in the manner shown when blended with the ethers.
The catalytically cracked gasoline is produced by the catalytic cracking of a higher boiling hydrocarbon oil at temperatures in the range of 900 to about 1100 F., pressures in the range of 5 to'about 75'p.s.i.g. The cracking may be etfected in a fluid bed reactor, moving bed reactor or a riser reactor such as described in U. S. application Serial Number 586,105, filed May 21, 1956. The products from the cracking reactor are preferably separated into a normally gaseous fraction including substantial amounts of olefins, a catalytically cracked gasoline boiling up to about 185-25.0 R, and a heavy naphtha. This naphtha fraction is advantageously catalytically reformed and then combined with the blend of the hydrogenated catalytically cracked gasoline and the ether. The reforming may be affected by any of the known catalytic reforming processes. In a typical case the naptha is Platformed by a platinum-alumina-halogencatalyst at a temperature of 900-960 F. and pressure of 150-450 p.s.i.g. in the presence of recycled hydrogen.
Since the effect of a given amount of ether in the blend with the catalytically cracked gasoline is considerably improved by the partial reduction in the bromine number, the amount of reformed naphtha or other blending materials that may be incorporated to produce the finished gasoline of desired octane number may be increased; such components can in fact become the chief component in the gasoline. On the other hand, the advantage can be exploited in a difierent way. Thus, in view of the greater effectiveness of the amount of ether used the naphtha may be used in the same amount but may be reformed to a lesser degree as by the use of less severe reforming conditions, thereby lowering the reforming cost and improving the yield of reformed product.
The catalytically cracked gasoline is catalytically hydrogenated to reduce the bromine number at least to some degree and preferably to about the extents indicated. The bromine number is initially at least around 100. The hydrogenation may be effected with any of the various hydrogenation catalysts hitherto used for hydrogenation of petroleum products. Preferred catalysts are prepared by incorporating oxides or sulfides of one or more to the metals Ou, Co, Ni, Cr, Mo, W with an aluminous carrier material such asactivated alumina or microporous silica-alumina composites. The hydrogenation is efiectd at temperatures in the range of about 300 to 800 F., preferably about 500 to 700 F. The process may be carried out under pressures from slightly above atmospheric up to about 100 atmospheres. Under any given set of these conditions the rate of gasoline and hydrogen feed to the hydrogenation zone may be adjusted such that the desired degree of bromine number reduction is obtained. When effecting the hydrogenation under conditions to obtain a bromine number reduction of from about 50 to about there is a substantial exothermic heat effect which makes control of the temperature difiicult. This difiiculty can be minimized by using two small reactors in series .with'intermediate cooling of the reactant stream, or by adding to the feed a sizable amount of a substantially inert hydrocarbon diluent material having a sufliciently different boiling range that it may be separated from the partially hydrogenated catalytically cracked gasoline product by a subsequent fractional distillation.
The ether is advantageously made from the olefinic gaseous fraction mentioned above. This is advantageous in two respects. -In the first place this materially upgrades this gaseous product. In the second place the conversion of propylene and/or butylene to ethers reduces the amount of polymers which would otherwise be made fi'om them. This is advantageous since the polymers tend to degrade the quality of the gasoline in which they are blended.
The conversion of the gaseous olefins to ethers may be efiected by reacting them with a suitable alcohol such as methanol, or isopropanol by known methods e.g., as described in U.S. Patent No. 2,480,940 to Leum. A very desirable arrangement which produces large Volumes of the ether is to hydrate the propylene to isopropyl alcohol (a known process) and then react this alcohol with the butylene-butane fraction or additional propylene whereby isopropyl tertiary butyl ether or di-isopropyl ether is formed. Still larger volumes of the ether may be produced but at increased cost, by reacting both the propylene and the isobutylene with methanol to produce methyl isopropyl and methyl tertiary butyl ethers.
The etherification reaction normally does not consume all of the alcohol in the reaction mixture. Unreacted alcohol may be removed by water washing the ether product or in some cases by distillation. The ethers in question are normally liquid and are easily separated from the unreacted hydrocarbons (e.g., butane-butylene fractions) by a simple distillation.
Example A reduced petroleum wa vacuum flashed to produce a flashed distillate and the residue was then propane deasphalted to produce a deasphalted oil. The flashed distillate and deasphalted oil were catalytically cracked together in a commercial fluidized catalyst cracking unit using a synthetic silica-alumina cracking catalyst. The product was fractionated in the plant in the normal manner to separate a propane-propylene fraction, a butanebutylene fraction, a catalytically cracked gasoline having the properties given above, and various heavier materials.
Separate propanepropylene and butane-butylene fractions from a different source were reacted with methanol and isopropanol to produce methyl isopropyl ether, methyl tertiary butyl ether, diisopropyl ether, and isopropyl tertiary butyl ether.
The catalytically cracked gasoline was partially bydrogenated with a commercial Co-Mo/alumina catalyst at 536-608 F. and 200 p.s.i.g. at a hydrogen to oil mole ratio of 2.8 and a liquid hourly space velocity of 4 to reduce the bromine number by 63%,
To the thus partially hydrogenated catalytically cracked gasoline there was added 44% by volume of methyl tertiary butyl ether giving a blend containing about 31% of the ether. To this blend there was then added 104% by volume of a reformed naphtha having an F1-3 octane number of 96.8 which it will be noted is considerably below that of the catalytically cracked gasoline (100.9). The resulting blend had an F13 octane number of 100.4. When di-isopropyl ether was substituted the octane number of the blend was 100.0. isopropyl tertiary butyl ether was found equally effective as the methyl tertiary butyl ether and methyl tertiary amyl ether and ethyl tertiary butyl ether were intermediate the isopropyl tertiary butyl and di-isopropyl ether.
The F-l-S octane number is the CFR designation for the ASTM Research Octane Number D908-47T for the material containing 3 cc. of ethyl fluid per US, gallon. The bromine numbers were determined by the meth od described by A. Polgar et al. in Organic Analysis, vol. III, p. 237, Interscience Publishers, N.Y.
I claim as my invention:
1. In the production of high octane automotive motor gasoline the improvement which comprises catalytically cracking a hydrocarbon oil boiling above gasoline with a silica-alumina type cracking catalyst, separating from the products of said cracking a fraction of normally gaseous hydrocarbons containing olefins, an unsaturated catalytically cracked gasoline having an end point between about 180 and 250 F., and a catalytically cracked naphtha, catalytically hydrogenating said catalytically cracked gasoline until its bromine number is reduced between about 25 and and combining with the partially hydrogenated catalytically cracked gasoline at least over 12% by volume thereof of a saturated alkyl ether boiling in the range of about 89 F. to F.
2. Process according to claim 1 further characterized in that the said catalytically cracked naphtha is catalytically reformed to an F-1-3 octane number less than that of the catalytically cracked gasoline ether mixture and is then combined with said mixture.
3. Process according to claim 1 in which the ether is methyl tertiary butyl ether.
4. Process according to claim 1 in which the ether is methyl isopropyl ether.
5. Process according to claim 1 in which the ether is di-isopropyl ether.
6. Process according to claim 1 in which the ether is isopropyl tertiary butyl ether.
7. Process according to claim 1 in which the ether is methyl tertiary amyl ether.
8. In the production of high octane automotive motor gasoline the improvement which comprises catalytically cracking a hydrocarbon oil boiling above gasoline with a silica-alumina type cracking catalyst, separating from the products of said cracking a fraction of normally gaseous hydrocarbons containing olefins, an unsaturated catalytically cracked gasoline having an end point between about 180 and 250 F., and a catalytically cracked naphtha, catalytically hydrogenating said catalytically cracked gasoline until its bromine number is reduced between about 25 and 95%, and combining with the partially hydrogenated catalytically cracked gasoline at least over 12% by volume thereof of a saturated alkyl ether boiling in the range of about 89 F. to 180 F., the extent of bromine number reduction being correlated with the percent by volume of ether in the blend approximately as follows:
Percent bromine Percent ether in blend: No. reduction as' follows:
cataly-tlcally cracked 'gasolme about 7 %v. ether required to be partial hydrogenadded to the unation to bromine hydrogenated catnumber reduction, alytically cracked percent gasoline 8 References Cited in the file of this patent UNITED .STATES PATENTS M'arschner, July 14, 1942 Thomas "Aug. 11, 1942 Evans et a1. -Oct 22, 1946 .Hill Feb. 17, 1948 Haenselet a1. Apr. 3, 1956 FOREIGN PATENTS Great Britain Apr. 14, 1936 Great Britain June 13, 1939 OTHER REFERENCES 15 Progress in Petroleum Technology, page 368, published whereby the amount of ether actually required is reduced. by American Chemical Society, August 7, 1951. 2
Claims (1)
1. IN THE PRODUCTION OF HIGH OCTANE AUTOMOTIVE MOTOR GASOLINE THE IMPROVEMENT WHICH COMPRISES CATALYTICALLY CRACKING A HYDROCARBON OIL BOILING ABOVE GASOLINE WITH A SILICA-ALUMINA TYPE CRACKING CATALYST, SEPARATING FROM THE PRODUCTS OF SAID CRACKING A FRACTION OF NORMALLY GASEOUS HYDROCARBON CONTAINING OLEFINS, AN UNSATURATED CATALYTICALLY CRACKED GASOLINE HAVING AN END POINT BETWEEN ABOUT 180 AND 250*F., AND A CATALYTICALLY CRACKED NAPHTHA, CATALYTICALLY HYDROGENATING SAID CATALYTICALLY CRACKED GASOLINE UNTIL ITS BROMINE NUMBER IS
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL103620D NL103620C (en) | 1957-06-27 | ||
US668303A US2952612A (en) | 1957-06-27 | 1957-06-27 | Production of high octane motor fuel with an alkyl ether additive |
GB20396/58A GB829072A (en) | 1957-06-27 | 1958-06-25 | Production of high octane motor gasoline |
DEN15267A DE1103493B (en) | 1957-06-27 | 1958-06-25 | Process for making high octane gasoline |
FR1207533D FR1207533A (en) | 1957-06-27 | 1958-06-25 | High octane fuel manufacturing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US668303A US2952612A (en) | 1957-06-27 | 1957-06-27 | Production of high octane motor fuel with an alkyl ether additive |
Publications (1)
Publication Number | Publication Date |
---|---|
US2952612A true US2952612A (en) | 1960-09-13 |
Family
ID=24681802
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US668303A Expired - Lifetime US2952612A (en) | 1957-06-27 | 1957-06-27 | Production of high octane motor fuel with an alkyl ether additive |
Country Status (5)
Country | Link |
---|---|
US (1) | US2952612A (en) |
DE (1) | DE1103493B (en) |
FR (1) | FR1207533A (en) |
GB (1) | GB829072A (en) |
NL (1) | NL103620C (en) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3482952A (en) * | 1968-04-29 | 1969-12-09 | Chevron Res | Process for production of gasoline |
US3836342A (en) * | 1972-06-23 | 1974-09-17 | Sun Research Development | Gasoline containing a methyl phenol and an ether |
US3849082A (en) * | 1970-06-26 | 1974-11-19 | Chevron Res | Hydrocarbon conversion process |
DE2444528A1 (en) * | 1973-09-18 | 1975-03-20 | Magyar Asvanyolaj Es Foeldgaz | FUEL FOR ENGINES WITH SPARK IGNITION AND ADDITIVES FOR THESE |
US3912463A (en) * | 1970-06-26 | 1975-10-14 | Chevron Res | Hydrocarbon conversion process |
US3976437A (en) * | 1972-06-23 | 1976-08-24 | Sun Ventures, Inc. | Composition comprising a methyl phenol and an ether for gasoline fuels |
FR2411881A1 (en) * | 1977-12-16 | 1979-07-13 | Gulf Canada Ltd | PREPARATION OF A HYDROCARBON GASOLINE CONTAINING TERTIARY AMYL AMYL ETHER |
US4244704A (en) * | 1980-01-04 | 1981-01-13 | Texaco Inc. | Gasoline composition |
US4252541A (en) * | 1975-11-28 | 1981-02-24 | Texaco Inc. | Method for preparation of ethers |
FR2477570A1 (en) * | 1980-03-10 | 1981-09-11 | Inst Francais Du Petrole | HYDROGENATION AND ETHERIFICATION OF AN UNCURRENT C5 CUTTING OF HYDROCARBONS IN ORDER TO IMPROVE OCTANE INDEX AND REDUCE THE MONO-OLEFINS CONTENT |
DE3116734A1 (en) * | 1981-04-28 | 1982-11-18 | Veba Oel AG, 4660 Gelsenkirchen-Buer | CARBURETOR FUEL |
US4519809A (en) * | 1984-04-23 | 1985-05-28 | Exxon Research & Engineering Co. | Method for reducing water sensitivity of ether containing gasoline compositions |
WO1993016150A1 (en) * | 1992-02-07 | 1993-08-19 | Nrg-Technologies, L.P. | Composition and method for producing a multiple boiling point ether gasoline component |
US5256167A (en) * | 1991-05-21 | 1993-10-26 | Nippon Oil Co., Ltd. | Gasoline |
US5401280A (en) * | 1992-10-14 | 1995-03-28 | Nippon Oil Co., Ltd. | Lead-free, high-octane gasoline |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB445503A (en) * | 1935-06-04 | 1936-04-14 | Standard Oil Dev Co | Improvements relating to motor fuels |
GB507246A (en) * | 1937-02-06 | 1939-06-13 | Standard Oil Dev Co | An improved manufacture of motor fuels |
US2289716A (en) * | 1939-10-19 | 1942-07-14 | Standard Oil Co | Catalytic motor fuel production |
US2292677A (en) * | 1939-05-17 | 1942-08-11 | Universal Oil Prod Co | Catalytic conversion of hydrocarbons |
US2409746A (en) * | 1940-07-31 | 1946-10-22 | Shell Dev | Motor fuels |
US2436170A (en) * | 1946-01-29 | 1948-02-17 | Standard Oil Dev Co | Finishing of aviation naphthas |
US2740751A (en) * | 1952-02-23 | 1956-04-03 | Universal Oil Prod Co | Reforming of both straight run and cracked gasolines to provide high octane fuels |
-
0
- NL NL103620D patent/NL103620C/xx active
-
1957
- 1957-06-27 US US668303A patent/US2952612A/en not_active Expired - Lifetime
-
1958
- 1958-06-25 GB GB20396/58A patent/GB829072A/en not_active Expired
- 1958-06-25 DE DEN15267A patent/DE1103493B/en active Pending
- 1958-06-25 FR FR1207533D patent/FR1207533A/en not_active Expired
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB445503A (en) * | 1935-06-04 | 1936-04-14 | Standard Oil Dev Co | Improvements relating to motor fuels |
GB507246A (en) * | 1937-02-06 | 1939-06-13 | Standard Oil Dev Co | An improved manufacture of motor fuels |
US2292677A (en) * | 1939-05-17 | 1942-08-11 | Universal Oil Prod Co | Catalytic conversion of hydrocarbons |
US2289716A (en) * | 1939-10-19 | 1942-07-14 | Standard Oil Co | Catalytic motor fuel production |
US2409746A (en) * | 1940-07-31 | 1946-10-22 | Shell Dev | Motor fuels |
US2436170A (en) * | 1946-01-29 | 1948-02-17 | Standard Oil Dev Co | Finishing of aviation naphthas |
US2740751A (en) * | 1952-02-23 | 1956-04-03 | Universal Oil Prod Co | Reforming of both straight run and cracked gasolines to provide high octane fuels |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3482952A (en) * | 1968-04-29 | 1969-12-09 | Chevron Res | Process for production of gasoline |
US3849082A (en) * | 1970-06-26 | 1974-11-19 | Chevron Res | Hydrocarbon conversion process |
US3912463A (en) * | 1970-06-26 | 1975-10-14 | Chevron Res | Hydrocarbon conversion process |
US3836342A (en) * | 1972-06-23 | 1974-09-17 | Sun Research Development | Gasoline containing a methyl phenol and an ether |
US3976437A (en) * | 1972-06-23 | 1976-08-24 | Sun Ventures, Inc. | Composition comprising a methyl phenol and an ether for gasoline fuels |
DE2444528A1 (en) * | 1973-09-18 | 1975-03-20 | Magyar Asvanyolaj Es Foeldgaz | FUEL FOR ENGINES WITH SPARK IGNITION AND ADDITIVES FOR THESE |
US4252541A (en) * | 1975-11-28 | 1981-02-24 | Texaco Inc. | Method for preparation of ethers |
FR2411881A1 (en) * | 1977-12-16 | 1979-07-13 | Gulf Canada Ltd | PREPARATION OF A HYDROCARBON GASOLINE CONTAINING TERTIARY AMYL AMYL ETHER |
US4244704A (en) * | 1980-01-04 | 1981-01-13 | Texaco Inc. | Gasoline composition |
FR2477570A1 (en) * | 1980-03-10 | 1981-09-11 | Inst Francais Du Petrole | HYDROGENATION AND ETHERIFICATION OF AN UNCURRENT C5 CUTTING OF HYDROCARBONS IN ORDER TO IMPROVE OCTANE INDEX AND REDUCE THE MONO-OLEFINS CONTENT |
EP0035935B1 (en) * | 1980-03-10 | 1983-12-28 | Institut Français du Pétrole | Hydrogenation and etherification of an unsaturated c5 hydrocarbon fraction in order to improve the octane index and reduce the content of mono-olefins |
DE3116734A1 (en) * | 1981-04-28 | 1982-11-18 | Veba Oel AG, 4660 Gelsenkirchen-Buer | CARBURETOR FUEL |
US4468233A (en) * | 1981-04-28 | 1984-08-28 | Veba Oel Ag | Motor fuel containing tert-butyl ethers |
US4519809A (en) * | 1984-04-23 | 1985-05-28 | Exxon Research & Engineering Co. | Method for reducing water sensitivity of ether containing gasoline compositions |
US5256167A (en) * | 1991-05-21 | 1993-10-26 | Nippon Oil Co., Ltd. | Gasoline |
WO1993016150A1 (en) * | 1992-02-07 | 1993-08-19 | Nrg-Technologies, L.P. | Composition and method for producing a multiple boiling point ether gasoline component |
US6017371A (en) * | 1992-02-07 | 2000-01-25 | Nrg Technologies, Inc. | Composition and method for producing a multiple boiling point ether gasoline component |
US5401280A (en) * | 1992-10-14 | 1995-03-28 | Nippon Oil Co., Ltd. | Lead-free, high-octane gasoline |
Also Published As
Publication number | Publication date |
---|---|
NL103620C (en) | |
DE1103493B (en) | 1961-03-30 |
FR1207533A (en) | 1960-02-17 |
GB829072A (en) | 1960-02-24 |
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