US2145239A - Soluble oil - Google Patents

Soluble oil Download PDF

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Publication number
US2145239A
US2145239A US47143A US4714335A US2145239A US 2145239 A US2145239 A US 2145239A US 47143 A US47143 A US 47143A US 4714335 A US4714335 A US 4714335A US 2145239 A US2145239 A US 2145239A
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US
United States
Prior art keywords
oil
naphthenate
triethanolamine
soap
soluble
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
Application number
US47143A
Inventor
Marcellus T Flaxman
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Union Oil Company of California
Original Assignee
Union Oil Company of California
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Union Oil Company of California filed Critical Union Oil Company of California
Priority to US47143A priority Critical patent/US2145239A/en
Application granted granted Critical
Publication of US2145239A publication Critical patent/US2145239A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • 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
    • C10M173/00Lubricating compositions containing more than 10% water
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K23/00Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
    • C09K23/017Mixtures of 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
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
    • 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
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/022Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
    • 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
    • C10M2207/16Naphthenic acids
    • 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/22Metal working with essential removal of material, e.g. cutting, grinding or drilling
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/46Textile oils
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/01Emulsions, colloids, or micelles
    • 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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S516/00Colloid systems and wetting agents; subcombinations thereof; processes of
    • Y10S516/01Wetting, emulsifying, dispersing, or stabilizing agents
    • Y10S516/06Protein or carboxylic compound containing

Definitions

  • This invention relates to the so-called soluble oils or emulsifiable oils which have various uses such as for textile lubricants, cutting oils for machine purposes, spray oils and the like, and ap- 5 plies particularly to those for making stable-type emulsions.
  • the soluble oil is prepared from mineral oil and potassium or sodium naphthenate where the mixture is nearly anhydrous, that is, contains preferably not over about 2% of water.
  • triethanolamine naphthenate, oleate or other soap soluble in "the oil may be used to replace an equally small proportion of the sodium or potassium naphthenate.
  • a very small percentage of the triethanolamine soap reduces the pour point of the substantially anhydrous soap solution to a desirable degree.
  • the invention may be stated as residing in a substantially dehydrated solution of a potassium or sodium naphthenate in mineral oil and also as residing in such a nearly anhydrous solution containing a small quantity of defined triethanolamine soap to increase the fluidity to a workable consistency where a substantial quantity 40 of sodium or potassium naphthenate is present forming an otherwise too viscous mass.
  • potassium naphthenate ,or sodium naphthenate of comparatively low water content may be combined with mineral oil in a quantity ranging from 5% or 10% up to 25% or 30% or thereabouts to yield a substantially anhydrous solution which may thereafter be emulsified in water.
  • An average amount of potassium naphthenate for most purposes is about 15%, but when larger amounts are employed the solution of the soap in the oil is ordinarily too viscous for practical uses unless larger amounts of triethanolamine soap are added, but in that event both excess materials are without substantial advantage and merely I have serve to increase cost.
  • approximately A9 of triethanolamine naphthenate or other describ'ed soap is added.
  • the viscosity of the solution is reduced from a semi-gelatinous mass. to a fluid body which 5 pours readily.
  • a product would contain about of mineral oil, 14.5% of potassium naphthenate, and 0.5% of the triethanolamine naphthenate or other soap.
  • the triethanolamine naphthenate may be varied 10 from about 0.1% to 1.5% of the total.
  • the minimum limit is that which will satisfactorily increase fluidity of the solution.
  • the maximum limit of the triethanolamine soap is that which does not aifect the stability of the emulsion sub- 15 sequently produced with the soluble oil and water,
  • the maximum limit is in the order of a. few percent of the soluble oil.
  • naphthenic acids are obtained from a mineral oil having a Saybolt Universal viscosity of 200 seconds at F., and these acids are saponified with potassium hydroxide to produce the potassium naphthenate.
  • the acids employed are usually recovered in a large 'quantity of mineral oil, for example in about equal amounts.
  • the caustic solution is added and the temperature raised to effect saponification, for example, to 30 212 F. If necessary to reduce the water content to the minimum necessary to yield the required minimum water content of the final product, a high temperature may be used, e. g. 300 F.
  • This potassium naphthenate then has added thereto 35 the necessary additional quantities of oil, such as a mineral oil having a viscosity of seconds at 100 F., or other kindred mineral oil. Since such a solution pours'with difficulty at normal temperatures, an addition of 0.5% of triethanol- 4o amine naphthenate is made with agitation to effect thorough distribution and this reduces the viscosity so. that the resultant soluble oil then pours readily at normal temperatures.
  • oil such as a mineral oil having a viscosity of seconds at 100 F., or other kindred mineral oil. Since such a solution pours'with difficulty at normal temperatures, an addition of 0.5% of triethanol- 4o amine naphthenate is made with agitation to effect thorough distribution and this reduces the viscosity so. that the resultant soluble oil then pours readily at normal temperatures.
  • the mixture before ad- 45 dition of further oil, and the triethanolamine naphthenate it may be dehydrated as by heating after the addition of either or both of these.
  • the preferred water content is about 1%, but 2% is not objectionable, and in some cases the mixture 50 may be considered as substantially anhydrous for the present purpose if the water does not exceed about 5%.
  • triethanolamine naphthenate other triethanolamine soaps may be employed with satisfactory results, these including triethanolamine oleate, stearate, and similar soaps from fatty acids of similar molecular weight and generally similar character, which soaps are soluble in the oil.
  • triethanolamine oleate stearate
  • similar soaps from fatty acids of similar molecular weight and generally similar character, which soaps are soluble in the oil.
  • alcohols and the like may also be added to impart other desirable properties such as rapid dispersability,

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Detergent Compositions (AREA)

Description

Patented Jan. 31, 1939 .r. y. a
so UBLEoni.
' Marcellus T.'Flaxinan, wilmington,Calif assign- U or to Union Oil Company of'California,
Angeles, Calif., a corporation of-California No Drawing. Application oetobe'r' 28, 1935'," Serial No. 47,143
3 Claims.
This invention relates to the so-called soluble oils or emulsifiable oils which have various uses such as for textile lubricants, cutting oils for machine purposes, spray oils and the like, and ap- 5 plies particularly to those for making stable-type emulsions.
Heretofore, in the preparation of various emulsifiable and soluble oils it has been a common practice to employ a soap as the emulsifying agent for the various mineral oil fractions, and in turn to introduce a mutual solvent which acts as a bonding agent to hold thesoap and the oil together.
I have found that for many purposes the use of a mutual solvent or bonding agent can be eliminated if the soluble oil is prepared from mineral oil and potassium or sodium naphthenate where the mixture is nearly anhydrous, that is, contains preferably not over about 2% of water.
However, such a solution of soap and oil is semigelatinous at ordinary temperatures and therefore is too viscous for most purposes. found further that in order to reduce the viscosity as desired or to control the viscosity readily, a
small proportion of triethanolamine naphthenate, oleate or other soap soluble in "the oil, may be used to replace an equally small proportion of the sodium or potassium naphthenate. In other words, a very small percentage of the triethanolamine soap reduces the pour point of the substantially anhydrous soap solution to a desirable degree.
The invention, therefore, may be stated as residing in a substantially dehydrated solution of a potassium or sodium naphthenate in mineral oil and also as residing in such a nearly anhydrous solution containing a small quantity of defined triethanolamine soap to increase the fluidity to a workable consistency where a substantial quantity 40 of sodium or potassium naphthenate is present forming an otherwise too viscous mass.
In practice I find that potassium naphthenate ,or sodium naphthenate of comparatively low water content may be combined with mineral oil in a quantity ranging from 5% or 10% up to 25% or 30% or thereabouts to yield a substantially anhydrous solution which may thereafter be emulsified in water. An average amount of potassium naphthenate for most purposes is about 15%, but when larger amounts are employed the solution of the soap in the oil is ordinarily too viscous for practical uses unless larger amounts of triethanolamine soap are added, but in that event both excess materials are without substantial advantage and merely I have serve to increase cost. According to this invention, approximately A9 of triethanolamine naphthenate or other describ'ed soap is added. As
a result, the viscosity of the solution is reduced from a semi-gelatinous mass. to a fluid body which 5 pours readily. Thus, such a product would contain about of mineral oil, 14.5% of potassium naphthenate, and 0.5% of the triethanolamine naphthenate or other soap. In general, the triethanolamine naphthenate may be varied 10 from about 0.1% to 1.5% of the total. The minimum limit is that which will satisfactorily increase fluidity of the solution. The maximum limit of the triethanolamine soap is that which does not aifect the stability of the emulsion sub- 15 sequently produced with the soluble oil and water,
or that which is economically feasible. In genera], the maximum limit is in the order of a. few percent of the soluble oil.
As an example of one method of operation ac- 20 cording to this invention, naphthenic acids are obtained from a mineral oil having a Saybolt Universal viscosity of 200 seconds at F., and these acids are saponified with potassium hydroxide to produce the potassium naphthenate. 25 The acids employed are usually recovered in a large 'quantity of mineral oil, for example in about equal amounts. To this material the caustic solution is added and the temperature raised to effect saponification, for example, to 30 212 F. If necessary to reduce the water content to the minimum necessary to yield the required minimum water content of the final product, a high temperature may be used, e. g. 300 F. This potassium naphthenate then has added thereto 35 the necessary additional quantities of oil, such as a mineral oil having a viscosity of seconds at 100 F., or other kindred mineral oil. Since such a solution pours'with difficulty at normal temperatures, an addition of 0.5% of triethanol- 4o amine naphthenate is made with agitation to effect thorough distribution and this reduces the viscosity so. that the resultant soluble oil then pours readily at normal temperatures.
Instead of dehydrating the mixture before ad- 45 dition of further oil, and the triethanolamine naphthenate, it may be dehydrated as by heating after the addition of either or both of these. The preferred water content is about 1%, but 2% is not objectionable, and in some cases the mixture 50 may be considered as substantially anhydrous for the present purpose if the water does not exceed about 5%.
By addition of a few percent of such soluble oil to water accompaniedwith agitation, a quite stable emulsion is produced suitable for various uses to which this type of oil is adapted, such as in the textile and metal working industries.
Instead of triethanolamine naphthenate, other triethanolamine soaps may be employed with satisfactory results, these including triethanolamine oleate, stearate, and similar soaps from fatty acids of similar molecular weight and generally similar character, which soaps are soluble in the oil. In addition to these materials, alcohols and the like may also be added to impart other desirable properties such as rapid dispersability,
these including such alcohols as ethyl alcohol,
ethylene glycol and similar alcoholic products.
It is to be understood that the above disclosures are merely illustrative of the generic the triethanolamine soap is a naphthenate.
MARCELLUS T. FLAXMAN.
US47143A 1935-10-28 1935-10-28 Soluble oil Expired - Lifetime US2145239A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2978408A (en) * 1956-01-09 1961-04-04 Procter & Gamble Scorch resistant textile softening finish composition
US3071544A (en) * 1959-08-14 1963-01-01 Sun Oil Co Emulsifiable mixtures of mineral oil and esters

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2978408A (en) * 1956-01-09 1961-04-04 Procter & Gamble Scorch resistant textile softening finish composition
US3071544A (en) * 1959-08-14 1963-01-01 Sun Oil Co Emulsifiable mixtures of mineral oil and esters

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