US2852356A - Aviation fuel - Google Patents
Aviation fuel Download PDFInfo
- Publication number
- US2852356A US2852356A US435929A US43592954A US2852356A US 2852356 A US2852356 A US 2852356A US 435929 A US435929 A US 435929A US 43592954 A US43592954 A US 43592954A US 2852356 A US2852356 A US 2852356A
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- Prior art keywords
- distillate
- gum
- gasoline
- aviation fuel
- catalytic
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Classifications
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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
- C10L1/04—Liquid carbonaceous fuels essentially based on blends of hydrocarbons
- C10L1/06—Liquid carbonaceous fuels essentially based on blends of hydrocarbons for spark ignition
Definitions
- Tetra-ethyl lead is conventionally, added to improve the octane number. There are no set proportions inwhich each of these ingredients are used and in any given instance the proportion of the ingredients is so adjusted so that the resultant blend will meet the various specifications for aviation gasoline at the lowest possible cost.
- the alkylate is the ingredient primarily responsible for the high octane number of the blend but is relatively expensive. Any of the different alkylates can be used and the chemical composition of several useful alkylates is given on pages 472 to 474 of 'Sachanen, Conversion of Fetroleum, Reinhold Publishing Corporation (1948).
- the basic gasolines which may be either straight-run, natural, or catalytically cracked gasolines, are desirable constituents of aviation gasoline because of their low cost but, in the case of catalytically cracked gasoline, it has been found that the gasoline requires a special treatment before it can be used in any significant quantity in an aviation fuel. This is because catalytically cracked gasoline is a notorious gum former and, when used in a significant quantity, produces a blend which does not meet gum specifications.
- the treatments devised to improve the gum forming tendency of catalytically cracked gasoline are quite cumbersome and fairly costly. They include, for example, sulfuric acid treatment, mild hydrogenation of the catalytic gasoline, and the recracking of the catalytic gasoline in a catalytic reactor. Because of the disadvantages inherent in any and all of these procedures it is apparent that the art would welcome a simpler method of treating catalytically cracked gasoline in order to render it suitable for inclusion in an aviation fuel in a significant quantity.
- One of the basic gasolines which has received prior consideration as a component of aviation fuel is a catalytically cracked distillate boiling in the range of approximately 100 to 430 F. which is obtained from the catalytic cracking of crude petroleum.
- This distillate can be produced at relatively low cost and is available in large quantities. It is believed that the use of the distillate as a component in aviation gasoline was first considered during the second World War when the heavy demand for aviation fuel necessitated the inclusion of large amounts of catalytic distillate and at one time during the war, it is reported that the total amount of aviation gasoline comprised as much as one-third catalytic distillate.
- the composition of the present invention comprises an aviation gasoline containing a significant quantity up to about 15% by volume of the total fuel of a heart-cut of a c'atalytically cracked distillate, said heart-cut having a boiling range of about 150 to 338 F.
- the invention provides a simplified solution to an existing problem since a simple fractional distillation of the catalytic distillate has inherent advantages both in processing cost and ease of operation over the previously used treatments used to reduce the gum forming tendencies of the catalytic distillate.
- the catalytically cracked distillate referred to is one of the products of the catalytic cracking process. It is a well known material made by a well known process.
- a typical catalytic distillate has the following properties:
- the aviation fuel of the present invention preferably comprises from about 68% to about 73% of an alkylate, from about 4 to about 9% of isopentane, from about 7 to about 12% of a straight-run gasoline, and from about 5 to about 15 of the aforementioned heart-cut.
- Example 1 There was blended together 82 barrels of a light alkylate having a boiling range of 95 to 325 P. which had been prepared by the alkylation of isobutane with butyl ene, using a sulfuric acid catalyst, 5 barrels of isopentane, and
- the two examples taken in comparison show that the untreated catalytic distillate cannot be incorporated in aviation fuel in any quantity without resulting in a blend that fails to meet gum specifications.
- the heartcut can be used in a significant quantity and when the octane rating of the blend permits, up to about 15% by volume of the heart-cut can 'be utilized based on the weight of gasoline.
- the success of the invention can be explained in retrospect by the postulation that the diolefins of the catalytic distillate are predominantly in the lighter-and heavier ends. Since the diolefins are known to be gum formers, their removal by fractionation renders the resulting heart-cut relatively free from gum-forming components. Hence, the heart-cut can be used in relatively large amounts in aviation fuel.
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
United States Patent AVIATION FUEL Fred Lee Lichtenfels, Toledo, Ohio, assignor to The Standard Oil Company, Cleveland, Ohio, a corporation of Ohio No Drawing. Application June 10, 1954 Serial No. 435,929
3 Claims. (Cl. 44-80) Tetra-ethyl lead is conventionally, added to improve the octane number. There are no set proportions inwhich each of these ingredients are used and in any given instance the proportion of the ingredients is so adjusted so that the resultant blend will meet the various specifications for aviation gasoline at the lowest possible cost.
The alkylate is the ingredient primarily responsible for the high octane number of the blend but is relatively expensive. Any of the different alkylates can be used and the chemical composition of several useful alkylates is given on pages 472 to 474 of 'Sachanen, Conversion of Fetroleum, Reinhold Publishing Corporation (1948).
The basic gasolines, which may be either straight-run, natural, or catalytically cracked gasolines, are desirable constituents of aviation gasoline because of their low cost but, in the case of catalytically cracked gasoline, it has been found that the gasoline requires a special treatment before it can be used in any significant quantity in an aviation fuel. This is because catalytically cracked gasoline is a notorious gum former and, when used in a significant quantity, produces a blend which does not meet gum specifications. The treatments devised to improve the gum forming tendency of catalytically cracked gasoline are quite cumbersome and fairly costly. They include, for example, sulfuric acid treatment, mild hydrogenation of the catalytic gasoline, and the recracking of the catalytic gasoline in a catalytic reactor. Because of the disadvantages inherent in any and all of these procedures it is apparent that the art would welcome a simpler method of treating catalytically cracked gasoline in order to render it suitable for inclusion in an aviation fuel in a significant quantity.
One of the basic gasolines which has received prior consideration as a component of aviation fuel is a catalytically cracked distillate boiling in the range of approximately 100 to 430 F. which is obtained from the catalytic cracking of crude petroleum. This distillate can be produced at relatively low cost and is available in large quantities. It is believed that the use of the distillate as a component in aviation gasoline was first considered during the second World War when the heavy demand for aviation fuel necessitated the inclusion of large amounts of catalytic distillate and at one time during the war, it is reported that the total amount of aviation gasoline comprised as much as one-third catalytic distillate.
In the first attempts to employ the catalytic distillate as an ingredient of aviation gasoline it was found as heretofore indicated that the distillate possessed such high gum forming tendencies that it could not be used without a further treatment because aviation gasoline specificationsimpose much more restrictive stability requirements than do motor gasoline specifications. It was further found that not even the most effective oxidation and gum inhibitors were capable of limiting the gum formation in the average catalytically cracked distillate to a suflicient extent to permit the use of the distillate in aviation fuel in any significant quantity. Therefore, it was necessary to subject the distillate to one of the aforementioned treatments. The subjecting of the distillate to any one of the treatments was sufficient to improve the stability sufficiently to permit the inclusion of up to as much as 33% by volume of the catalytic distillate in aviation fuel.
In accordance with the present invention, I have found surprisingly that if the untreated catalytic distillate is subjected to a fractionation to remove the lighter and heavier ends, the resulting heart-cut (approximate boiling point range, 150 to 338 F.) has suificient stability that it can be incorporated in aviation fuel in a relatively large quantity while still producing an aviation fuel which meets gum specifications. Accordingly, the composition of the present invention comprises an aviation gasoline containing a significant quantity up to about 15% by volume of the total fuel of a heart-cut of a c'atalytically cracked distillate, said heart-cut having a boiling range of about 150 to 338 F.
It can readily be seen that the invention provides a simplified solution to an existing problem since a simple fractional distillation of the catalytic distillate has inherent advantages both in processing cost and ease of operation over the previously used treatments used to reduce the gum forming tendencies of the catalytic distillate.
The catalytically cracked distillate referred to is one of the products of the catalytic cracking process. It is a well known material made by a well known process. A typical catalytic distillate has the following properties:
ASTM distillation, boiling range:
IBP
EP F 420-435 Octane No. F-l clear 88-92 Bromine No 35-60 ASTM gum (mgm./100 ml.) 3-5 Gravity AP I) 54-60 A typical hydrocarbon analysis of the catalytic distillate is as follows:
Fraction: Volume percent Aromatics u 15-30 Olefins 20-35 Saturates 35-55 The heart-cut of the catalytic distillate which is used as an ingredient of aviation fuel in accordance with the present invention is derived from the catalytic distillate by simple fractionation to isolate a material boiling in the approximate range of to 338 F.
The aviation fuel of the present invention preferably comprises from about 68% to about 73% of an alkylate, from about 4 to about 9% of isopentane, from about 7 to about 12% of a straight-run gasoline, and from about 5 to about 15 of the aforementioned heart-cut.
In order to illustrate the invention, the following examples are presented. In the examples, the performance rating data were obtained according to ASTM tests D6l4-49T and D909-49T.
Example 1 There was blended together 82 barrels of a light alkylate having a boiling range of 95 to 325 P. which had been prepared by the alkylation of isobutane with butyl ene, using a sulfuric acid catalyst, 5 barrels of isopentane, and
13 barrels of a straight-run gasoline having a boiling range of 120 to 290 F. The blend was found to have a performance rating of 106/130 by knock test methods. In order to dilute the blend to a 100/ 130 rating, there was added 17 barrels of a heart-cut of a catalytic distillate having a boiling range of about 100 to 435 F., the heart-cut having a boiling range of about 150 to 338 F.
In the ASTM gum test, the blend left a residue of only 2 mgm. per hundred ml. which is sufficient to pass the gum specifications for aviation fuel.
Example 1.4
When 17 barrels of the untreated catalytic distillate was substituted for the 17 barrels of heart-cut used in Example 1, the resultant blend had a very poor gum rating and in the ASTM gurn test left a residue of about 15 mgm. per hundred ml. which exceeds gum specifications for aviation gasoline.
The two examples taken in comparison show that the untreated catalytic distillate cannot be incorporated in aviation fuel in any quantity without resulting in a blend that fails to meet gum specifications. However, the heartcut can be used in a significant quantity and when the octane rating of the blend permits, up to about 15% by volume of the heart-cut can 'be utilized based on the weight of gasoline.
In theory, the success of the invention can be explained in retrospect by the postulation that the diolefins of the catalytic distillate are predominantly in the lighter-and heavier ends. Since the diolefins are known to be gum formers, their removal by fractionation renders the resulting heart-cut relatively free from gum-forming components. Hence, the heart-cut can be used in relatively large amounts in aviation fuel.
I claim:
1. An aviation fuel containing a significant amount up to about 15% by volume of the total fuel of a heart-cutboiling in the range of 150 F. to 380 F., fractionated from a catalytically cracked distillate having the following inspection:
IBP F 90-100 over PL. 120-135 50% over PL. 235-250 90% over F 390-405 EP F 420-435 Octane No. F-1 clear 88-92 Bromine N0 35-60 ASTM gum (mgm./100 ml.) 3-5 Gravity API) 54-60 Aromatics percent -30 Olefins do -35 Saturates do -55 IBP F -100 10% over F 120-135 50% over F 235-250 90% F 390-405 EP PL. 420-435 Octane No. F-l clear 88-92 Bromine No 35-60 ASTM gum (mgm./l00 ml.) 3-5 Gravity API) 54-60 Aromatics percent 15-30 Olefins do 20-35 Saturates do 35-55 3. An aviation fuel containing 82 parts of a light alkylate boiling in the range of F. to 350 F. obtained by the alkylation of isobutane with butylenes, 5 parts of isopentane, 13 parts of straight-run gasoline boiling in the range of F. to 290 F. and 17 parts of a heart-cut boiling in the range of F. to 380 F., fractionated from a catalytically cracked distillate having the following inspection:
IBP 90-100 10% over R. 120-135 50% over F 235-250 90% over F 390-405 EP F 420-435 Octane No. F-l clear 88-92 Bromine No 35-60 ASTM gum (mgm./l00 n11.) 3-5 Gravity API) 54-60 Aromatics "percent" 15-30 Olefins do 20-35 Saturates do 35-55 References Cited in the file of this patent UNITED STATES PATENTS 2,406,394- Newton Aug. 27, 1946 2,466,334- Skelton Apr. 5, 1949 2,470,445 Purdy May 17, 1949 2,629,685 Lifson et al. Feb. 24, 1953 OTHER REFERENCES Sachanen: Chemical Constituents of Petroleum, pages 261, 262, 264 and 265. Published by Reinhold Publishing Corp., New York, N. Y., 1945.
UNITED STATES PATENT OFFICE CERTEFEQATE 6i 'QURREQHQN Patent No, 2,852,356 September 16, 1958 Fred Lee Lichtenfels It is hereby certified that error appears in the-printed specification of the above numbered patent requiring correction and that the said Letters Patent should read as corrected below,
Column 4, line 12, after "90%" insert over (SEAL) Attest:
KARL H, AXLINE ROBERT C. WATSON Commissioner of Patents Attesting Officer
Claims (1)
1. AN AVIATION FUEL CONTAINING A SIGNIFICANT AMOUNT UP TO ABOUT 15% BY VOLUME OF THE TOTAL FUEL OF A HEART-CUT BOILING IN THE RANGE OF 150*F. TO 380*F., FRACTIONATE FROM A CATALYTICALLY CRACKED DISTILLATE HAVING THE FOLLOWING INSPECTION:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US435929A US2852356A (en) | 1954-06-10 | 1954-06-10 | Aviation fuel |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US435929A US2852356A (en) | 1954-06-10 | 1954-06-10 | Aviation fuel |
Publications (1)
Publication Number | Publication Date |
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US2852356A true US2852356A (en) | 1958-09-16 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US435929A Expired - Lifetime US2852356A (en) | 1954-06-10 | 1954-06-10 | Aviation fuel |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3034878A (en) * | 1957-12-26 | 1962-05-15 | Exxon Research Engineering Co | High octane motor fuels |
US3038792A (en) * | 1959-03-20 | 1962-06-12 | Ethyl Corp | Gasoline fuel |
US3148959A (en) * | 1960-03-31 | 1964-09-15 | California Research Corp | Gasoline composition containing tetravinyl lead and aromatic hydrocarbons |
US3195992A (en) * | 1959-03-27 | 1965-07-20 | California Research Corp | Gasoline composition containing lead compounds |
US3316071A (en) * | 1958-09-26 | 1967-04-25 | Chevron Res | Gasoline composition |
US3901664A (en) * | 1971-06-25 | 1975-08-26 | Chevron Res | Motor fuel |
US3988122A (en) * | 1971-06-25 | 1976-10-26 | Chevron Research Company | Motor fuel composition |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2406394A (en) * | 1943-01-08 | 1946-08-27 | Houdry Process Corp | Production of aviation gasoline |
US2466334A (en) * | 1944-08-10 | 1949-04-05 | Texas Co | Method of producing synthetic fuel |
US2470445A (en) * | 1947-10-29 | 1949-05-17 | Standard Oil Dev Co | Production of high octane number aviation gasoline |
US2629685A (en) * | 1949-10-29 | 1953-02-24 | Standard Oil Dev Co | Aviation fuel and method of preparing same |
-
1954
- 1954-06-10 US US435929A patent/US2852356A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2406394A (en) * | 1943-01-08 | 1946-08-27 | Houdry Process Corp | Production of aviation gasoline |
US2466334A (en) * | 1944-08-10 | 1949-04-05 | Texas Co | Method of producing synthetic fuel |
US2470445A (en) * | 1947-10-29 | 1949-05-17 | Standard Oil Dev Co | Production of high octane number aviation gasoline |
US2629685A (en) * | 1949-10-29 | 1953-02-24 | Standard Oil Dev Co | Aviation fuel and method of preparing same |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3034878A (en) * | 1957-12-26 | 1962-05-15 | Exxon Research Engineering Co | High octane motor fuels |
US3316071A (en) * | 1958-09-26 | 1967-04-25 | Chevron Res | Gasoline composition |
US3038792A (en) * | 1959-03-20 | 1962-06-12 | Ethyl Corp | Gasoline fuel |
US3195992A (en) * | 1959-03-27 | 1965-07-20 | California Research Corp | Gasoline composition containing lead compounds |
US3148959A (en) * | 1960-03-31 | 1964-09-15 | California Research Corp | Gasoline composition containing tetravinyl lead and aromatic hydrocarbons |
US3901664A (en) * | 1971-06-25 | 1975-08-26 | Chevron Res | Motor fuel |
US3988122A (en) * | 1971-06-25 | 1976-10-26 | Chevron Research Company | Motor fuel composition |
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