US2063575A - Dispersing of phenolphthalein in mineral lubricating oils - Google Patents

Dispersing of phenolphthalein in mineral lubricating oils Download PDF

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US2063575A
US2063575A US718529A US71852934A US2063575A US 2063575 A US2063575 A US 2063575A US 718529 A US718529 A US 718529A US 71852934 A US71852934 A US 71852934A US 2063575 A US2063575 A US 2063575A
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phenolphthalein
oil
dispersing
alcohol
mineral
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Adams Elmer Wade
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Standard Oil Co
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M171/00Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
    • C10M171/007Coloured or dyes-containing lubricant compositions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/025Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with condensed rings
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/142Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings polycarboxylic
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/284Esters of aromatic monocarboxylic acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/285Esters of aromatic polycarboxylic acids
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/04Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
    • C10M2211/044Acids; Salts or esters thereof
    • CCHEMISTRY; METALLURGY
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2215/042Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/066Arylene diamines
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/14Containing carbon-to-nitrogen double bounds, e.g. guanidines, hydrazones, semicarbazones
    • CCHEMISTRY; METALLURGY
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/221Six-membered rings containing nitrogen and carbon only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/225Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • CCHEMISTRY; METALLURGY
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/225Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • C10M2215/226Morpholines
    • CCHEMISTRY; METALLURGY
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/30Heterocyclic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/21Hydrocarbon

Definitions

  • My invention relates to the dispersion of preferentially alcohol soluble materials in mineral oils.' More particularly it relates to the dispersion of preferentially alcohol soluble materials- 10 particularly lubricating oils, by the use of alcohols having molecular weights greater than that of the propanols. My invention also relates to the products resulting from mynew method of dispersion.
  • an alcohol preferably a mono-hydroxy alcohol, having a molecular weight greater than that of the propanols, for instance: the butanols, the pentanols, the hexanols, the heptanols or mixtures of any of 55 these with each other and/or with up to about 50% of methanol and/or ethanol.
  • the amount of phenolphthalein and the amount of alcohol can be varied within wide limits, thus, for instance, from 0.05 ounce to one pound or even more of phenolphthalein and from five ounces to gallons or even more of alcohol having a molecular weight greater than that of the propanols, preferably normal butanol, can be used per 10,000 gallons of oil.
  • This method can be used in dispersing phenolphthalein in other mineral -oils,-for instance: gasoline, kerosene, furnace oil, fuel oil, etc.
  • Other preferentially water or alcohol soluble indicators or dye -intermediates can thus be distributed, for instance: phenylenediamine, methyl orange (the sodium salt of helianthine), bromophenol blue (tetrabromophenolsulfonphthalein),
  • the same method can be utilized forintro ducing preferentially water or alcohol soluble dyestuffs in mineral oils, for instance: spirit dyes, such as alizarine (dihydroxy anthroquanone (1,2), eosine '(tetrabromofiuoresceinl and its alkaline salts, fluorescein (resorcinphthalein) auramin, malachite green (tetramethyldi-.paminotriphenyl carbohydride' hydrochloride) cyanine, etc. Still other preferentially water or alcohol soluble materials such as antioxidants, antiknock improvers, etc. can thus be introduced.
  • spirit dyes such as alizarine (dihydroxy anthroquanone (1,2), eosine '(tetrabromofiuoresceinl and its alkaline salts, fluorescein (resorcinphthalein) auramin, malachite green (tetramethyldi-.paminotripheny
  • the amount ofpreferentially alcohol soluble material tobe added will, of course, vary greatly with the potency of the particular material chosen, the result to be accomplished, etc. In genera] the amount will range from, say, 0.01 ounce to five pounds, or preferably .05 ounce to one pound, per 10,000 gallons of mineral oil.
  • the amount of higher alcohol necessary to disperse this material in accordance with my invention will also vary greatly but, in general, may range from one ounce to 25 gallons, or preferably from five ounces to one gallon per.10,000 gallons of mineral oil.
  • a method of dispersing phenolphthalein in mineral lubricating oil comprising dissolving ap proximately 0.25 ounce of phenolphthalein in approximately one pint of normal butanol, introducing the solution thus formed into approx mately 10,000 gallons of mineral lubricating oil and distributing the said solution throughout the said oil by blowing with air.
  • Fluid oils comprising the following materials in approximately the following proportions: mineral oil, 10,000 gallons; preferentially alcohol soluble material selected from the group consisting of the dyestuffs, the dye intermediates, the indicators, the antioxidants and the antiknock improvers, from 0.01 ounce to five pounds; a monohydroxy alcohol having a molecular weight greator than that of propanol, from one ounce to 25 gallons.
  • Fluid oils comprising the following materials in approximately the following proportions: mineral lubricating oil, 10,000 gallons; phenolphthalein, 0.25 ounce; normal butanol, one pint.
  • a fluid oil composition comprising a solution of mineral lubricating oil, phenolphthalein and normal butyl alcohol.
  • a fluid oil composition comprising a solution of mineral lubricating oil, phenolphthalein and a normally liquid aliphatic alcohol having a molecular weight greater than that of the propanols.

Description

Patented Dec. 8, 1936 UNITED STATES DISPERSING OF PHENOLPHTHALEIN IN IVIINERAL LUBRIQATING OILS Elmer Wade Adams, Hammond, Ind., assignor to Standard Oil Company, Chicago, 111., a corporation of Indiana No Drawing. Application March 31, 1934,
Serial No. 718,529
. 8 Claims. My invention relates to the dispersion of preferentially alcohol soluble materials in mineral oils.' More particularly it relates to the dispersion of preferentially alcohol soluble materials- 10 particularly lubricating oils, by the use of alcohols having molecular weights greater than that of the propanols. My invention also relates to the products resulting from mynew method of dispersion.
It has been proposed to provide a means for the identification of mineral oils by incorporating therein asmall portion of an indicator or other relatively colorless material which will form a detectable color on treatment with a'suit- 20 able chemical reagent. Thus, for instance, it
has been proposed to provide a means for identifying lubricating oils by incorporating therein a trace of phenolphthalein (dihydroxyphthalophenone) which will form a brilliant red colora- 25 tion when the oil is-shaken with an aqueous alkaline solution. The idea is simple but it' has not been satisfactorily accomplished in the past due to the difliculty of incorporating the phenolphthalein in the oil. Phenolphthalein, being 80 preferentially soluble in water and the alcohols rather than in mineral oils, cannot readily be incorporated directly in the oil. Neither can it be incorporated satisfactorily in solution in such a material as ethanol. Thus, for example, when 0.25 ounce of phenolphthalein is dissolved in one pint of ethanol, the solution is added to 10,000
gallons of lubricating oil, and the phenolphthalein is distributed in the oil by the normal air blowing method, it .is found that the phenolphthalein concentration in the oil diminishes gradually, due to preciptation, thereby destroying its quantitative value in detecting adulteration. Furthermore, when the solution of phenol- 45 phthalein in oil is filtered, for instance through ordinary filter paper, the phenolphthalein is completely removed. V
I have overcome these difficulties by first dissolving the phenolphthalein in an alcohol, preferably a mono-hydroxy alcohol, having a molecular weight greater than that of the propanols, for instance: the butanols, the pentanols, the hexanols, the heptanols or mixtures of any of 55 these with each other and/or with up to about 50% of methanol and/or ethanol. I prefer, however, to use normal butanol.
Thus, for instance, when 0.25 ounce of phenolphthalein is dissolved in one pint of normal butanol and the solution thus formed is added to 10,000 gallons of lubricating oil it can be distributed uniformly throughout the oil by agitating by the normal air blowing method without precipitation of the phenolphthalein. Furthermore, when the oil solution thus formed by the use of normal butanol is filtered, for instance through ordinary filter paper, the phenolphthalein is not removed as was the case when it was added in ethanol solution. I am not aware just what the reason is for the peculiar action of this relatively minute amount of higher alcohol, but I believe it may be attributed, to the formation of a loose chemical compound or alcoholate between the phenolphthalein and the higher alcohol.
The amount of phenolphthalein and the amount of alcohol can be varied within wide limits, thus, for instance, from 0.05 ounce to one pound or even more of phenolphthalein and from five ounces to gallons or even more of alcohol having a molecular weight greater than that of the propanols, preferably normal butanol, can be used per 10,000 gallons of oil. The
upper limits of both the phenolphthalein and the .7 I
alcohol are determined by economic factors.
This method can be used in dispersing phenolphthalein in other mineral -oils,--for instance: gasoline, kerosene, furnace oil, fuel oil, etc. Other preferentially water or alcohol soluble indicators or dye -intermediates can thus be distributed, for instance: phenylenediamine, methyl orange (the sodium salt of helianthine), bromophenol blue (tetrabromophenolsulfonphthalein),
etc.
The same method can be utilized forintro ducing preferentially water or alcohol soluble dyestuffs in mineral oils, for instance: spirit dyes, such as alizarine (dihydroxy anthroquanone (1,2), eosine '(tetrabromofiuoresceinl and its alkaline salts, fluorescein (resorcinphthalein) auramin, malachite green (tetramethyldi-.paminotriphenyl carbohydride' hydrochloride) cyanine, etc. Still other preferentially water or alcohol soluble materials such as antioxidants, antiknock improvers, etc. can thus be introduced.
The amount ofpreferentially alcohol soluble material tobe added will, of course, vary greatly with the potency of the particular material chosen, the result to be accomplished, etc. In genera] the amount will range from, say, 0.01 ounce to five pounds, or preferably .05 ounce to one pound, per 10,000 gallons of mineral oil. The amount of higher alcohol necessary to disperse this material in accordance with my invention will also vary greatly but, in general, may range from one ounce to 25 gallons, or preferably from five ounces to one gallon per.10,000 gallons of mineral oil.
While I have described my invention in connection with certain specific embodiments and in connection with certain theories of operation it is to be understood that these are by way of illustration rather than by way of limitation and I do not intend to be limited thereby except to the scope of the appended claims.
I claim: I
1. A method of dispersing phenolphthalein in mineral lubricating oil, comprising dissolving ap proximately 0.25 ounce of phenolphthalein in approximately one pint of normal butanol, introducing the solution thus formed into approx mately 10,000 gallons of mineral lubricating oil and distributing the said solution throughout the said oil by blowing with air.
2. Fluid oils, comprising the following materials in approximately the following proportions: mineral oil, 10,000 gallons; preferentially alcohol soluble material selected from the group consisting of the dyestuffs, the dye intermediates, the indicators, the antioxidants and the antiknock improvers, from 0.01 ounce to five pounds; a monohydroxy alcohol having a molecular weight greator than that of propanol, from one ounce to 25 gallons.
3. Fluid oils, comprising the following materials in approximately the following proportions: mineral lubricating oil, 10,000 gallons; phenolphthalein, 0.25 ounce; normal butanol, one pint.
4. The method of dispersing phenolphthalein in mineral lubricating oils comprising dissolving said phenolphthalein in normal butyl alcohol and introducing the solution thus formed into the mineral oil.
5. A fluid oil composition comprising a solution of mineral lubricating oil, phenolphthalein and normal butyl alcohol.
6. The method of dispersing phenolphthalein in a mineral lubricating oil comprising dissolving said phenolphthalein in a normally liquid aliphatic alcohol having a molecular weight greater than that of the propanols and introducing the solution thus formed into the mineral oil.
7. The method of dispersing phenolphthalein in mineral lubricating oils comprising dissolving sail phenolphthalein in a normally liquid aliphatic alcohol having a molecular weight greater than that of the propanols, introducing the solution thus formed into the mineral oil, and agitating the admixture by blowing with air.
- 8. A fluid oil composition comprising a solution of mineral lubricating oil, phenolphthalein and a normally liquid aliphatic alcohol having a molecular weight greater than that of the propanols.
ELMER WADE ADAMS.
CERTIFICATE OF CORRECTION.
atent No. 2,065,575. December 8, 1936.
ELMER WADE ADAMS.
It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction as follows: Page 2, strike out all of claim 2 and for the claim numbers "3" "4" 5" "6", "'7" and "8" read 2, 3, 4, 5, 6, and 7 respectively; and that the said Letters Patent should be read with these corrections therein that the same may conform to the record of the case in the Patent Office.
Signed and sealed this 16th day of February, A. D. 1937.
Henry Van Arsdale Seal) Acting Commissioner of Patents.
US718529A 1934-03-31 1934-03-31 Dispersing of phenolphthalein in mineral lubricating oils Expired - Lifetime US2063575A (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2451022A (en) * 1944-02-28 1948-10-12 Frederick C Dohrmann Color changing antiseptic composition
FR2501044A1 (en) * 1981-03-04 1982-09-10 Machugh John 3,3-BIS- (β-HYDROXYPHENYL) -PHTALID MEDICINAL PRODUCT AND PROCESS FOR PREPARING THE SAME
EP0311790A1 (en) * 1987-09-18 1989-04-19 BASF Aktiengesellschaft Marked mineral oil product, and process to mark mineral oil products
WO1996000272A1 (en) * 1994-06-27 1996-01-04 Basf Aktiengesellschaft Use of leucotriarylmethanes for marking hydrocarbons
WO1996022345A1 (en) * 1995-01-20 1996-07-25 United Color Manufacturing, Inc. Fluorescent petroleum markers
WO1996032462A1 (en) * 1995-04-13 1996-10-17 United Color Manufacturing, Inc. Colorless petroleum markers
WO1996032461A1 (en) * 1995-04-13 1996-10-17 United Color Manufacturing, Inc. Developer system for base reactable petroleum fuel markers
US6482651B1 (en) 1999-06-30 2002-11-19 United Color Manufacturing, Inc. Aromatic esters for marking or tagging petroleum products

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2451022A (en) * 1944-02-28 1948-10-12 Frederick C Dohrmann Color changing antiseptic composition
FR2501044A1 (en) * 1981-03-04 1982-09-10 Machugh John 3,3-BIS- (β-HYDROXYPHENYL) -PHTALID MEDICINAL PRODUCT AND PROCESS FOR PREPARING THE SAME
EP0073758A1 (en) * 1981-03-04 1983-03-16 John Edward Mchugh Treatment of inflammatory viral infections, acne, dermatitis and arthritis conditions.
EP0073758A4 (en) * 1981-03-04 1983-07-04 John Edward Mchugh Treatment of inflammatory viral infections, acne, dermatitis and arthritis conditions.
EP0311790A1 (en) * 1987-09-18 1989-04-19 BASF Aktiengesellschaft Marked mineral oil product, and process to mark mineral oil products
WO1996000272A1 (en) * 1994-06-27 1996-01-04 Basf Aktiengesellschaft Use of leucotriarylmethanes for marking hydrocarbons
WO1996022345A1 (en) * 1995-01-20 1996-07-25 United Color Manufacturing, Inc. Fluorescent petroleum markers
CN1086729C (en) * 1995-01-20 2002-06-26 联合颜料制造公司 Fluorescent petroleum markers
WO1996032462A1 (en) * 1995-04-13 1996-10-17 United Color Manufacturing, Inc. Colorless petroleum markers
WO1996032461A1 (en) * 1995-04-13 1996-10-17 United Color Manufacturing, Inc. Developer system for base reactable petroleum fuel markers
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