US2303819A - Stabilizing solution of tetra-alkyl lead compounds - Google Patents
Stabilizing solution of tetra-alkyl lead compounds Download PDFInfo
- Publication number
- US2303819A US2303819A US437087A US43708742A US2303819A US 2303819 A US2303819 A US 2303819A US 437087 A US437087 A US 437087A US 43708742 A US43708742 A US 43708742A US 2303819 A US2303819 A US 2303819A
- Authority
- US
- United States
- Prior art keywords
- gasoline
- tetra
- ethyl
- xylidine
- benzal
- 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
- 230000000087 stabilizing effect Effects 0.000 title description 9
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 27
- MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 20
- 239000012530 fluid Substances 0.000 description 15
- PCWRTXYUOHUXQG-UHFFFAOYSA-N n-(2,3-dimethylphenyl)-1-phenylmethanimine Chemical group CC1=CC=CC(N=CC=2C=CC=CC=2)=C1C PCWRTXYUOHUXQG-UHFFFAOYSA-N 0.000 description 15
- 230000015572 biosynthetic process Effects 0.000 description 8
- 239000000446 fuel Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- SUEYDGAIGNZTNZ-UHFFFAOYSA-N n-(3,5-dimethylphenyl)-1-phenylmethanimine Chemical group CC1=CC(C)=CC(N=CC=2C=CC=CC=2)=C1 SUEYDGAIGNZTNZ-UHFFFAOYSA-N 0.000 description 5
- 239000012141 concentrate Substances 0.000 description 4
- 150000002611 lead compounds Chemical class 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 230000006641 stabilisation Effects 0.000 description 3
- 238000011105 stabilization Methods 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000003389 potentiating effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
- CDULGHZNHURECF-UHFFFAOYSA-N 2,3-dimethylaniline 2,4-dimethylaniline 2,5-dimethylaniline 2,6-dimethylaniline 3,4-dimethylaniline 3,5-dimethylaniline Chemical group CC1=CC=C(N)C(C)=C1.CC1=CC=C(C)C(N)=C1.CC1=CC(C)=CC(N)=C1.CC1=CC=C(N)C=C1C.CC1=CC=CC(N)=C1C.CC1=CC=CC(C)=C1N CDULGHZNHURECF-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/24—Lead compounds
-
- 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
- C10L1/103—Liquid carbonaceous fuels containing additives stabilisation of anti-knock agents
Definitions
- This invention relates to stabilizing solutions of tetra-alkyl lead compounds; and it comprises a method of stabilizing said solutions particularly ethyl gasoline wherein the development of a hazy appearance is inhibited by adding to such solutions small quantities of benzal-xylidine; all as more fully hereinafter set forth and as claimed.
- ethyl gasoline It is customary in the production of so-called ethyl gasoline to add to a good grade of gaso-. line a small amount of a tetra-alkyl .lead compound, usually tetra-ethyl lead to reduce the tendency of the gasoline to cause knocking in high compression gasoline engines.
- the amount of tetra-alkyl lead compound added. to a gasoline depends upon the nature of the gasoline and the desired anti-knock rating.
- Tetra-ethyl lead is customarily added to the gasoline in the form of a concentrate called ethyl fluid which is a solution containing a mixture of tetra-ethyl lead, alkyl (ii-halide (e. g.
- alkyl di-halides ethyl di-bromide or'ethyl di-chloride or both
- a dye to impart a distinctive color to the gasoline.
- the function of the alkyl di-halides is to limit the formation of lead oxide from tetra-alkyl lead in the cylinders of the engine by forming volatile halides of lead which are carried out in the exhaust.
- the ethyl fluid is added to the gasofrom disadvantage.
- leaded gas0-- line tends to develop a hazy appearance upon standing, particularly in the presence of strong sunlight.
- ethyl gasoline may develop a perceptible haziness after an hour or two of exposure, and longer periods of exposure result in a very marked haziness and precipitation occurs. This phenomenon is also sometimes observed in the ethyl fluid itself.
- haze in gasoline is objectiona clear product; customers prefer a product which is crystal clear.
- a further and perhaps more important objection is that a reduction in the octane rating of gasoline is frequently associated with haze formation. Also damage is likely to occur in the fuel lines and carburetor.
- the development of haze in ethyl fluid itself is also objectionable, because when a hazy ethyl fluid is blended with gasoline to form ethyl gasoline, the haze is introduced into the fuel with all its attendant disadvantages.
- An object achieved by this invention is to provide solutions of tetra-alkyl lead compounds, such as ethyl fluid and ethyl gasoline which are stabilized against haze formation.
- Benzal-xylidine may be added with advantage to solutions generally of tetra-alkyl lead compounds and more particularly to all types of leaded gasoline.
- a manner of incorporating the henzal-xylidine in solutions of tetra-alkyl lead compound is not critical. It may be incorporated in the ethyl fluid at any stage during the preparation thereof, or it may be incorporated in the gasoline prior to the addition of ethyl fluid along with the ethyl fluid or subsequent to blending the ethyl fluid with the gasoline.
- xylidine incorporated in the ethyl fluid is generally somewhat greater than is required for stabilization of the concentrate so that by the addition of the usual small amount of ethyl fluid to the gasoline a suitable stabilizing amount of benzal-xylidine will be incorporated in the gasoline. Generally from 1 to per cent by weight,
- benzal-xylidine very satisfactorily stabilizes commercial tetra-ethyl lead concentrates, such as ethyl fluid and on adding the stabilized concentrate to gasoline to produce ethyl gasoline, a satisfactorily stabilized ethyl gasoline is obtained.
- benzal-xylidine is a more potent stabilizer against haze formation to its stabilizing properties has other prop erties which particularly recommend it for this use. It does not adversely affect the oxygen stability of the gasoline. Samples of cracked ethyl gasoline containing benzal-xylidine have been.
- benzal-xylidine can be readily prepared The following specific examples will serve to H- lustrate the excellent haze inhibiting properties of benzal-xylldine.
- Eazample.--Ethyl gasoline containing 0.1 per cent by weight of tetra-ethyl lead (added in the form of ethyl fuel comprising tetra-ethyl lead, ethylene dibromide and a dye) was treated with benzal-3,5-xylidine in the proportion of 20 pounds of the latter per thousand barrels of gasoline.' The resulting solution was exposed for-five hours to sunlight and the appearance of the gasoline was noted. At the endof the 5 hours exposure there was a small degree of haziness but a great improvement over the appearance of the v same gasoline containing no benzal-xylidine. This was considered a fair stabilization.
- the benzal-3,5-xylidine employed in the above example has the following formula and is a most efiective stabilizer for the present purposes.
- a most potent stabilizer it can be easily incorporated in the leaded gasoline; it being a liquid readily soluble in gasoline.
- a method of producing a. light-stable solution of a tetra-alkyl lead compound which comprises incorporating in said solution benzal-xylidine-in amount suflicient to inhibit the forma-.
- a method of producing a light-stable, antiknock motor fuel containing a tetra-alkyl lead compound which comprises incorporating in said motor fuel benzal-3,5-xylidine in an amount corresponding to 0.01 to 1.0 per cent by weight of the tetra-alkyl lead compound.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Patente ea. 1, 1942 STABHJZING SOLUTION OF TETRA-ALKYL LEAD COMPOUNDS Pennsylvania No Drawing.
Original application January 31,
,7 1940,,Serial No. 316,686. Divided and this application March 31, 1942, Serial No. 437,087
5 Claims.
This invention relates to stabilizing solutions of tetra-alkyl lead compounds; and it comprises a method of stabilizing said solutions particularly ethyl gasoline wherein the development of a hazy appearance is inhibited by adding to such solutions small quantities of benzal-xylidine; all as more fully hereinafter set forth and as claimed.
This application is a division of our copending application, Serial No. 316,686 as filed January 31, 1940.
It is customary in the production of so-called ethyl gasoline to add to a good grade of gaso-. line a small amount of a tetra-alkyl .lead compound, usually tetra-ethyl lead to reduce the tendency of the gasoline to cause knocking in high compression gasoline engines. The amount of tetra-alkyl lead compound added. to a gasoline depends upon the nature of the gasoline and the desired anti-knock rating. Tetra-ethyl lead is customarily added to the gasoline in the form of a concentrate called ethyl fluid which is a solution containing a mixture of tetra-ethyl lead, alkyl (ii-halide (e. g. ethyl di-bromide or'ethyl di-chloride or both) and a small amount of a dye to impart a distinctive color to the gasoline. The function of the alkyl di-halides is to limit the formation of lead oxide from tetra-alkyl lead in the cylinders of the engine by forming volatile halides of lead which are carried out in the exhaust. The ethyl fluid is added to the gasofrom disadvantage. For one thing, leaded gas0-- line tends to develop a hazy appearance upon standing, particularly in the presence of strong sunlight.- For example, in direct sunlight in the summer time, ethyl gasoline may develop a perceptible haziness after an hour or two of exposure, and longer periods of exposure result in a very marked haziness and precipitation occurs. This phenomenon is also sometimes observed in the ethyl fluid itself.
The formation of haze in gasoline is objectiona clear product; customers prefer a product which is crystal clear. A further and perhaps more important objection is that a reduction in the octane rating of gasoline is frequently associated with haze formation. Also damage is likely to occur in the fuel lines and carburetor. The development of haze in ethyl fluid itself is also objectionable, because when a hazy ethyl fluid is blended with gasoline to form ethyl gasoline, the haze is introduced into the fuel with all its attendant disadvantages.
An object achieved by this invention is to provide solutions of tetra-alkyl lead compounds, such as ethyl fluid and ethyl gasoline which are stabilized against haze formation.
We have found that haze formation in solutions of tetra-alkyl lead compounds, such as ethyl fluid and ethyl gasoline, can be very materially reduced by incorporating in such solutions small quantities, proportions on the amount of tetraalkyl lead compound in solution, of benzal-xylidine having the formula wherein R1 is a xylyl group and R2 is a phenyl group.
Benzal-xylidine may be added with advantage to solutions generally of tetra-alkyl lead compounds and more particularly to all types of leaded gasoline. A manner of incorporating the henzal-xylidine in solutions of tetra-alkyl lead compound is not critical. It may be incorporated in the ethyl fluid at any stage during the preparation thereof, or it may be incorporated in the gasoline prior to the addition of ethyl fluid along with the ethyl fluid or subsequent to blending the ethyl fluid with the gasoline.
Even very small amounts of benzal-xylidine are sufiicient to exert a substantial stabilizing effect against light in fluids containing tetra-alkyl lead compounds. In general with higher percentages of tetra-alkyl lead compounds, higher amounts of benzal-xylidine are required. Within the range of about 0.01 to aboutl per cent by weight of tetra-ethyl lead in gasoline, a substantial stabilizing effect is exerted by from about 3 to about 120 pounds of benzal-xylidine per thousand barrels of gasoline. Within the range from about 0.02 to about 0.40 per cent by weight of tetra-ethyl lead in solution, which represents a commercial range, it is advantageous to employ from about 10 to about 40 pounds of benzal-xylidine per thousand barrels of gasoline. Such u because the gasoline is not as marketable a 55 amounts will exert a marked stabilizing effect against light and will produce a commercial ethyl gasoline which is satisfactorily stable to light under the usual conditions of exposure.
. xylidine incorporated in the ethyl fluid is generally somewhat greater than is required for stabilization of the concentrate so that by the addition of the usual small amount of ethyl fluid to the gasoline a suitable stabilizing amount of benzal-xylidine will be incorporated in the gasoline. Generally from 1 to per cent by weight,
from compounds available on the market at a relatively low cost, and its mode of preparation is simple and inexpensive.
based on tetra-ethyl lead, of benzal-xylidine very satisfactorily stabilizes commercial tetra-ethyl lead concentrates, such as ethyl fluid and on adding the stabilized concentrate to gasoline to produce ethyl gasoline, a satisfactorily stabilized ethyl gasoline is obtained.
In general, we have found that benzal-xylidine is a more potent stabilizer against haze formation to its stabilizing properties has other prop erties which particularly recommend it for this use. It does not adversely affect the oxygen stability of the gasoline. Samples of cracked ethyl gasoline containing benzal-xylidine have been.
aged and tested for oxygen stability and by the copper dish method for gum formation. The presence of the benzal-xylidine did not promote either oxygen instability or gum formation. It is non-corrosive to common'packaging materials such as steel, zinc, copper and tin and is compatible with the dyes commonly used in ethyl gasoline to give it a distinctive appearance. It is sufliciently soluble in gasoline to accomplish the intended stabilization. Furthermore it is insoluble in water, which is a distinct advantage because contact with water will not result in I leaching the stabilizer out of the gasoline. Con
tinued storage of gasoline containing benzalxylidine does not affect its stabilizing properties.
. Also benzal-xylidine can be readily prepared The following specific examples will serve to H- lustrate the excellent haze inhibiting properties of benzal-xylldine.
Eazample.--Ethyl gasoline containing 0.1 per cent by weight of tetra-ethyl lead (added in the form of ethyl fuel comprising tetra-ethyl lead, ethylene dibromide and a dye) was treated with benzal-3,5-xylidine in the proportion of 20 pounds of the latter per thousand barrels of gasoline.' The resulting solution was exposed for-five hours to sunlight and the appearance of the gasoline was noted. At the endof the 5 hours exposure there was a small degree of haziness but a great improvement over the appearance of the v same gasoline containing no benzal-xylidine. This was considered a fair stabilization.
The benzal-3,5-xylidine employed in the above example has the following formula and is a most efiective stabilizer for the present purposes. In addition to being a most potent stabilizer it can be easily incorporated in the leaded gasoline; it being a liquid readily soluble in gasoline.
While our invention has been described herein with reference to certain specific embodiments at pecific examples thereof, we do not intend that our invention shall be limited'to such embodiments and examples except as hereinafter defined in the appended claims.
What we claim is:
1. A method of producing a. light-stable solution of a tetra-alkyl lead compound which comprises incorporating in said solution benzal-xylidine-in amount suflicient to inhibit the forma-.
tion of haze in said solution.
2. The method of claim 1 whenein the tetraalkyl lead compound is tetra-ethyl lead.
3. The method of claim 1 wherein the benzalzylidine compound i benzal-3,5-xylidine.
4. A method of producing a light-stable, antiknock motor fuel containing a tetra-alkyl lead compound which comprises incorporating in said motor fuel benzal-3,5-xylidine in an amount corresponding to 0.01 to 1.0 per cent by weight of the tetra-alkyl lead compound.
. 5. As an improved anti-knock motor fuel stable to light, a gasoline containing 0.02 to 0.4 per cent by weight of tetra-ethyl. lead and about 10 to 40 pounds of benzal-3,5-xylidine per 1,000 barrels of gasoline.
TROY LEE CAN'I'RELL. CARLTON LOUIS SUPLEE.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US437087A US2303819A (en) | 1940-01-31 | 1942-03-31 | Stabilizing solution of tetra-alkyl lead compounds |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US31668640A | 1940-01-31 | 1940-01-31 | |
US437087A US2303819A (en) | 1940-01-31 | 1942-03-31 | Stabilizing solution of tetra-alkyl lead compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
US2303819A true US2303819A (en) | 1942-12-01 |
Family
ID=26980545
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US437087A Expired - Lifetime US2303819A (en) | 1940-01-31 | 1942-03-31 | Stabilizing solution of tetra-alkyl lead compounds |
Country Status (1)
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2560489A (en) * | 1947-06-03 | 1951-07-10 | Gulf Oil Corp | Stabilized leaded gasolines |
US2885422A (en) * | 1956-01-27 | 1959-05-05 | Du Pont | Stabilization of organic isocyanates |
US3173871A (en) * | 1961-06-08 | 1965-03-16 | Castrol Ltd | Lubricating oils containing benzalcyclohexylamine and bis-phenols |
-
1942
- 1942-03-31 US US437087A patent/US2303819A/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2560489A (en) * | 1947-06-03 | 1951-07-10 | Gulf Oil Corp | Stabilized leaded gasolines |
US2885422A (en) * | 1956-01-27 | 1959-05-05 | Du Pont | Stabilization of organic isocyanates |
US3173871A (en) * | 1961-06-08 | 1965-03-16 | Castrol Ltd | Lubricating oils containing benzalcyclohexylamine and bis-phenols |
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