US2148758A - Prevention of gum development and the like in motor fuel - Google Patents

Prevention of gum development and the like in motor fuel Download PDF

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Publication number
US2148758A
US2148758A US23851A US2385135A US2148758A US 2148758 A US2148758 A US 2148758A US 23851 A US23851 A US 23851A US 2385135 A US2385135 A US 2385135A US 2148758 A US2148758 A US 2148758A
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United States
Prior art keywords
motor fuel
prevention
benzene
methyl
gum development
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Expired - Lifetime
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US23851A
Inventor
Herman P Lankelma
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Standard Oil Co
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Standard Oil Co
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Priority to US23851A priority Critical patent/US2148758A/en
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Publication of US2148758A publication Critical patent/US2148758A/en
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/182Organic compounds containing oxygen containing hydroxy groups; Salts thereof
    • C10L1/183Organic compounds containing oxygen containing hydroxy groups; Salts thereof at least one hydroxy group bound to an aromatic carbon atom

Definitions

  • the invention comprises the features hereinafter fully described, and particularly pointed out in the claims, the following description setting forth in detail certain illustrative embodiments of the invention, these being indicative, however. of but a few of the various ways in which the principle of the invention may be employed.
  • non-benzenold linking such as bensyl 1,2 dihydroxy benzene, dibenzyl 1,2 dihydroxy benzene, diphenylmethyl 1,2 dihydroxy benzene, triphenyl-methyl' 1,2 dihydroxybenzene,
  • the amount of the inhibitor agent may range from 0.0005 to 0.01 per cent. It may be dissolved directlyin themotor fuel, or wheredesired maybeiirst dissoivedinasolvent, such as alcohol, acetone, etc., and thus be incorporated.
  • Triphenyl methyl 1,2,3 trihydroxy benzene is incorporated in a cracked gasoline in similar amount.
  • a process of stabilizing cracked motor fuel against gum development and the like which comprises incorporating with the motor fuel a 15 small amount of a polyhydroxy benzene compound containing carbon, oxygen and hydrogen only and having the general formula CGHB-nOHmR,
  • the-OHm being hydroxyls in 1,2 or 1,2,3 positions and R being a cyclic hydrocarbon group from: 20
  • CHI polyhydroxy benzene compound containing carbon, oxygen and hydrogen only and having the general formula CaHs-nOI-ImR, the CHI: being hydroxyls in 1,2 or 1,2,3 positions and R'being a cyclic hydrocarbon group from: benzyl, dibenzyl, diphenyl-methyl, triphenyl-methyl.
  • a cracked motor fuel stabilized against gum development by addition of a small amount of benzyl 1,2 dihydroxy benzene.
  • a cracked motor fuel stabilized against gum development by addition of a small amount of triphenyl-methyl trihydron benzene in which two hydroxyls are in 1,2 position.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Liquid Carbonaceous Fuels (AREA)

Description

Patented Feb. 28, 1939 UNITED STATES PREVENTION OF GUM DEVELOPMENT AND THE LIKE IN MOTOR FUEL Herman I. Lankelma,0leveland, Ohio, assignor to The Standard Oil Company (Ohio), Cleveland, Ohio, a corporation of Ohio No Drawing. Application my 28, 1935, Serial No. 23,851
BOlaims.
The prevention of gum-formation in cracked motor fuel presents many peculiarities. Relatively few agents have been foimd having suf flcient inhibitory activity tube of passable utility. and of these some have defects along one line and others have defects in other respects. The matter is made further difficult by complications introduced by the prevalent more or less prolonged exposure of the gasoline to. sunlight in glass-reservoir curb pumps and the increasing usage in gasoline of various chemicals for reducing detonation, and for fancy artificial coloring. I have now found that certain aromatic organic compounds including alkyl structure afford very excellent results even in cases where the normal behavior of the motor fuel is disturbed by presence of other chemicals which effect gum sensitivity. To the accomplishment of the foregoing, and related ends, the invention, then, comprises the features hereinafter fully described, and particularly pointed out in the claims, the following description setting forth in detail certain illustrative embodiments of the invention, these being indicative, however. of but a few of the various ways in which the principle of the invention may be employed.
Inthemotqrfueltobetreatedthereisim corporated a small. amount of a polyhydroxy compound including a benzene ring having it carbon ring joined directly thereto by non-benzenold linking, such as bensyl 1,2 dihydroxy benzene, dibenzyl 1,2 dihydroxy benzene, diphenylmethyl 1,2 dihydroxy benzene, triphenyl-methyl' 1,2 dihydroxybenzene, triphenyl-methyl trihydroxy benzene in which'two hydroxyls are in 1,2 position, and analogues having hydrocarbon radicles on the benzene ring (ethyl, propyl, butyl, and such groups), tolyl-methyl 1,2 dihydroxy 4o benzene.
In general, the amount of the inhibitor agent may range from 0.0005 to 0.01 per cent. It may be dissolved directlyin themotor fuel, or wheredesired maybeiirst dissoivedinasolvent, such as alcohol, acetone, etc., and thus be incorporated.
As an example: with a cracked gasoline there is incorporated bensyl 1,2 dihydroxy benaene at the rate of 0.1 g. per gallon.
,As another example: 'I'riphenyl methyl 1,2 dihydroxy' benzene is admixed with a cracked gasoline at the rate of 0.1 g. per gallon.
As another example: Triphenyl methyl 1,2,3 trihydroxy benzene is incorporated in a cracked gasoline in similar amount. p 5
Other modes of applying the principle of the invention may be employed, change being made as regards the details described, provided however, the features stated in any of the following claims, or the equivalent of such, be employed. 10
I therefore particularly point out and distinctly claim as my invention:
1. A process of stabilizing cracked motor fuel against gum development and the like, which comprises incorporating with the motor fuel a 15 small amount of a polyhydroxy benzene compound containing carbon, oxygen and hydrogen only and having the general formula CGHB-nOHmR,
,the-OHm being hydroxyls in 1,2 or 1,2,3 positions and R being a cyclic hydrocarbon group from: 20
benzyl, dibenzyl, diphenyl-methyl, triphenyl 'methyl.
- polyhydroxy benzene compound containing carbon, oxygen and hydrogen only and having the general formula CaHs-nOI-ImR, the CHI: being hydroxyls in 1,2 or 1,2,3 positions and R'being a cyclic hydrocarbon group from: benzyl, dibenzyl, diphenyl-methyl, triphenyl-methyl.
5. A cracked motor fuel stabilized against gum development by addition of a small amount of benzyl 1,2 dihydroxy benzene.
6. A cracked motor fuel stabilized against gum development by addition of a small amount of triphenyl-methyl trihydron benzene in which two hydroxyls are in 1,2 position.
mmmnmnmms.
US23851A 1935-05-28 1935-05-28 Prevention of gum development and the like in motor fuel Expired - Lifetime US2148758A (en)

Priority Applications (1)

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US23851A US2148758A (en) 1935-05-28 1935-05-28 Prevention of gum development and the like in motor fuel

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US23851A US2148758A (en) 1935-05-28 1935-05-28 Prevention of gum development and the like in motor fuel

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2971013A (en) * 1957-03-13 1961-02-07 Diamond Alkali Co Polychlorobenzhydryl cresol

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2971013A (en) * 1957-03-13 1961-02-07 Diamond Alkali Co Polychlorobenzhydryl cresol

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