US2941944A - Soluble oil composition - Google Patents
Soluble oil composition Download PDFInfo
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- US2941944A US2941944A US571601A US57160156A US2941944A US 2941944 A US2941944 A US 2941944A US 571601 A US571601 A US 571601A US 57160156 A US57160156 A US 57160156A US 2941944 A US2941944 A US 2941944A
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- Prior art keywords
- oil
- soluble
- oils
- water
- soluble oil
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M173/00—Lubricating compositions containing more than 10% water
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- D—TEXTILES; PAPER
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- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M7/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/18—Natural waxes, e.g. ceresin, ozocerite, bees wax, carnauba; Degras
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
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- C10M2207/027—Neutral salts thereof
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- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/14—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/141—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings monocarboxylic
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- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/16—Naphthenic acids
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- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
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- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- C10M2207/283—Esters of polyhydroxy compounds
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- C10M2207/28—Esters
- C10M2207/286—Esters of polymerised unsaturated acids
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/404—Fatty vegetable or animal oils obtained from genetically modified species
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
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- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/08—Halogenated waxes
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/042—Amines, 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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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
- C10M2219/024—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of esters, e.g. fats
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/041—Triaryl phosphates
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/12—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of organic compounds, e.g. with PxSy, PxSyHal or PxOy
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- C10M2229/02—Unspecified siloxanes; Silicones
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- C10M2229/04—Siloxanes with specific structure
- C10M2229/05—Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
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- C10N2010/00—Metal present as such or in compounds
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/22—Metal working with essential removal of material, e.g. cutting, grinding or drilling
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/46—Textile oils
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- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/01—Emulsions, colloids, or micelles
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- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/40—Reduced friction resistance, lubricant properties; Sizing compositions
Definitions
- This invention relates to so-called soluble oils which are readily emulsified with water.
- Particular soluble oils are-used as cutting oils or as textile oils.
- the invention is particularly concerned with the provision of improved soluble oils containing minor proportions of triethanolamine benzoate, which may be made up with water to form aqueous emulsions having good wetting power and anti-corrosion properties.
- a cutting fluid must also, however, act as a lubricant to facilitate the motion of metal chips along the tool face to prevent the development of such high friction that welding takes place.
- cutting fluids are commonly emulsions of emulsible oils, the oils acting as the lubricant, and water acting as the coolant.
- the oils used are preferably mineral lubricating oils, to which known emulsifying agents have been added. They should pref- 2,941,944 Patented June 21, 1960 Where transparent emulsions are desired, sodium rosinates may also be added.
- Fungicides suchas sodium ortho phenylphenate may also be incorporated to inhibit the growth of undesirable organisms.
- the amount of triethanolamine benzoate required is generally between 0.05 and 5.0% by weight of the soluble oil, amounts between 0.25'and 2.5% by weight being particularly preferred. It is most conveniently incorporated in the oil by forming it in situ.
- benzoic acid may be dissolved in the lubricating oil and the necessary amount of triethanolamine may be added to neutralise this acid together with any naphthenic, fatty or rosin acids that may be present.
- spindle oil a Ininerallubricating oil of viscosity erably have viscosities of between 70 and 200 S.U.S. at c 100 F. Those having viscosities between 100 and 125 S.S.U. at 100 F. are particularly preferred.
- the invention comprises an improved soluble oil comprising a lubricating oil having a viscosity between 70 and 200 Saybolt Universal seconds at 100 F., preferably between 100 and 125 S.U.S., an emulsifying agent such as an oil-soluble metal petroleum sulphonate, preferably oil-soluble sodium petroleum sulphonates especially those having molecular Weights between 350 and 450, and a minor proportion of triethanolamine benzoate.
- a lubricating oil having a viscosity between 70 and 200 Saybolt Universal seconds at 100 F., preferably between 100 and 125 S.U.S.
- an emulsifying agent such as an oil-soluble metal petroleum sulphonate, preferably oil-soluble sodium petroleum sulphonates especially those having molecular Weights between 350 and 450, and a minor proportion of triethanolamine benzoate.
- the lubricating oil used for preparing these improved soluble oils may be hydrocarbon oils or synthetic oils from any source, but mineral oils are preferred.
- the soluble oil composition may also contain other materials commonly used in soluble oils.
- the soluble oil contains an emulsion stabiliser such as an alkali metal or alkaline earth metal naphthenate, preferably sodium naphthenate, or diethylene glycol or a lower aliphatic alcohol such as methyl, ethyl, isopropyl or butyl alcohol.
- an emulsion stabiliser such as an alkali metal or alkaline earth metal naphthenate, preferably sodium naphthenate, or diethylene glycol or a lower aliphatic alcohol such as methyl, ethyl, isopropyl or butyl alcohol.
- Anti-foaming agents such as silicone oils or vegetable waxes, particularly candelilla wax, may be incorporated.
- an oiliness or extreme pressure agent For certain applications where heavy duty conditions are encountered, it may be desirable to include an oiliness or extreme pressure agent.
- Typical agents which may be used are isopropyl oleate, tricresyl phosphate, chlorinated wax and fatty oils or sulphurised or phosphorised fatty oils.
- oil-soluble sodium petroleum sulphonates of molecular weight approximately 420 (in the form of a 70% solution of the :sulphonates in a mineral oil of viscosity 100 S.S.U. at 100 F.).
- the method of preparing the soluble oil was to blend together a major proportion of the spindle oil with the sulphonates and naphthenic acids, with heating to about to 9 C., to dissolve the sulphonates.
- the caustic soda in aqueous solution was then added to react with the naphthenic acids, after which the benzoic acid in solution of the rest of the spindle oil was introduced.
- the temperature was then allowed to drop down to about 40 C., before the addition of the 1% water and 0.9% isopropyl alcohol.
- oil-soluble sodium petroleum sulphonates (70% concentration in mineral oil, as in previous composition).
- the first figure given represents the area attacked as pared according to the present invention. H follows:
- p 0 represents less than /6.
- Example 1. a 1 represents /s-to /3.
- a soluble oil was prepared having the following 2 represents /3 to f l 3 represents greater than /3 82.5% spindle oil (as used in the previous compositions).
- spindle oil (as used in the previous compositions).
- t will be s a e compositions p p accord- 13.0% oil-soluble sodium petroleum sulphonates (70% mg to the present invention give hardly perceptible corconcentration in mineral oil, as in previous compo- IOSiOIl Over a fy area flffhe P sitions).
- the present invention accordingly comprises an mi- 2.5 naphthenic acids. proved soluble oil composition containing a mineral lubri- 0.4% caustic soda. eating oil having a viscosity between 70 and 200 S.S.U.
- the soluble oil composition may also contain a minor 0.3 triethanolamine. proportion of sodium benzoate as described and claimed 0.2% caustic soda. in British Patent No. 689,740issued July 14, 1950.
- the present invention also comprises soluble oil emul- 1.0% water, 0 sions formed from 3 to 80 parts by volume of water per 1.0% isopropyl alcohol (99%).
- a soluble oil composition consisting essentially of a sub ected to the COI'I'OSlOIl test standardised by the Institute base stock consisting of about 825% of a miner a1 lubri of Pejtroleum under h number eating oil having a viscosity of about 100 S.S.U. at 100 fi test i castflmn plates of dlmenswns.
- perature was controlled at 650 and the relative about 0.2% caustic soda, about 0.5% benzoic acid and humidity was controlled at 52%.
- the steel millings on each plate were flooded with 2 mgrn. of prepared emulsions of the appropriate soluble oil compositions, and the plates were left in the test chamber for 24 hours. At the end of this period the steel millings were removed about 1% each of water and isopropyl alcohol.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
- Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
Description
SOLUBLE OIL COMPOSITION William Denis Ervine, Tolworth, England, assignor t Esso Research and Engineering Company, a corporation of Delaware No Drawing. Filed Mar. 15, 1956, Ser. No. 571,601
Claims priority, application Great Britain Mar. 29, 1955 1 Claim. (Cl. 252-333.)
This invention relates to so-called soluble oils which are readily emulsified with water. Particular soluble oils are-used as cutting oils or as textile oils.
The invention is particularly concerned with the provision of improved soluble oils containing minor proportions of triethanolamine benzoate, which may be made up with water to form aqueous emulsions having good wetting power and anti-corrosion properties.
The principal function of a cutting fluid is the removal of heat from the metal being cut and the tool which is cutting it. This is necessary to avoid drawing the temper of the tool and distorting the workpiece. A cutting fluid must also, however, act as a lubricant to facilitate the motion of metal chips along the tool face to prevent the development of such high friction that welding takes place.
To fulfill these two functions, cutting fluids are commonly emulsions of emulsible oils, the oils acting as the lubricant, and water acting as the coolant. The oils used are preferably mineral lubricating oils, to which known emulsifying agents have been added. They should pref- 2,941,944 Patented June 21, 1960 Where transparent emulsions are desired, sodium rosinates may also be added.
Fungicides ,suchas sodium ortho phenylphenate may also be incorporated to inhibit the growth of undesirable organisms.
The amount of triethanolamine benzoate required is generally between 0.05 and 5.0% by weight of the soluble oil, amounts between 0.25'and 2.5% by weight being particularly preferred. It is most conveniently incorporated in the oil by forming it in situ. For example, benzoic acid may be dissolved in the lubricating oil and the necessary amount of triethanolamine may be added to neutralise this acid together with any naphthenic, fatty or rosin acids that may be present. V
Tests were conducted on a soluble 'oil composition containing sodium benzoate as the inhibitor as described and claimed in the specification of our earlier Patent No. 689,740, a soluble oil containing triethanolamine, and soluble oils containing triethanolamine benzoate according to the present invention, alone or with sodium benzoate. Each composition was prepared from samples SOLUBLE OIL CONTAINING SODIUM BENZOATE AS THE INHIBITOR A soluble oil composition was prepared, having the following formulation:
82.5% spindle oil (a Ininerallubricating oil of viscosity erably have viscosities of between 70 and 200 S.U.S. at c 100 F. Those having viscosities between 100 and 125 S.S.U. at 100 F. are particularly preferred.
Such fluids containing from about 3 to 80 parts of water per part of oil, are apt to be corrosive to the metal surfaces they encounter, but it has now been discovered that the incorporation of minor proportions of triethanolamine benzoate greatly reduces the tendency to cause corrosion.
, In its preferred embodiment, therefore, the invention comprises an improved soluble oil comprising a lubricating oil having a viscosity between 70 and 200 Saybolt Universal seconds at 100 F., preferably between 100 and 125 S.U.S., an emulsifying agent such as an oil-soluble metal petroleum sulphonate, preferably oil-soluble sodium petroleum sulphonates especially those having molecular Weights between 350 and 450, and a minor proportion of triethanolamine benzoate.
The lubricating oil used for preparing these improved soluble oils may be hydrocarbon oils or synthetic oils from any source, but mineral oils are preferred.
In addition to these essential ingredients, the soluble oil composition may also contain other materials commonly used in soluble oils.
For example, it is to be preferred that the soluble oil contains an emulsion stabiliser such as an alkali metal or alkaline earth metal naphthenate, preferably sodium naphthenate, or diethylene glycol or a lower aliphatic alcohol such as methyl, ethyl, isopropyl or butyl alcohol.
Anti-foaming agents such as silicone oils or vegetable waxes, particularly candelilla wax, may be incorporated.
For certain applications where heavy duty conditions are encountered, it may be desirable to include an oiliness or extreme pressure agent. Typical agents which may be used are isopropyl oleate, tricresyl phosphate, chlorinated wax and fatty oils or sulphurised or phosphorised fatty oils.
100 S.S.U. at 100 F.).
13.0% oil-soluble sodium petroleum sulphonates of molecular weight approximately 420 (in the form of a 70% solution of the :sulphonates in a mineral oil of viscosity 100 S.S.U. at 100 F.).
2.5% naphthenic acids.
0.4% caustic soda.
1.6% water.
To which is added: 0.3% benzoic acid. 0.1% caustic soda. 1.0% water. 0.9% isopropyl alcohol (99%).
The method of preparing the soluble oil was to blend together a major proportion of the spindle oil with the sulphonates and naphthenic acids, with heating to about to 9 C., to dissolve the sulphonates. The caustic soda in aqueous solution was then added to react with the naphthenic acids, after which the benzoic acid in solution of the rest of the spindle oil was introduced. The temperature was then allowed to drop down to about 40 C., before the addition of the 1% water and 0.9% isopropyl alcohol.
SOLUBLE OIL CONTAINING TRIETHANOLAMINR AS THE INHIBITOR A soluble oil was prepared having the following formulation: v
82.5% spindle oil (as used in the previous composition).
13.0% oil-soluble sodium petroleum sulphonates (70% concentration in mineral oil, as in previous composition).
2.5% naphthenic acids.
0.4% caustic soda.
1.6% water.
To which is added:
1.0% triethanolamine. 0.9% isopropyl alcohol (99%).
The method of preparation was similar, except that triethanolamine was used instead of benzoic acid.
Two further soluble oil compositions were then pre- 4 rated according to the area attacked and the intensity of the corrosion in that area.
The first figure given represents the area attacked as pared according to the present invention. H follows:
p 0 represents less than /6. Example 1., a 1 represents /s-to /3. A soluble oil was prepared having the following 2 represents /3 to f l 3 represents greater than /3 82.5% spindle oil (as used in the previous compositions).
13.0% oil-soluble sodium petroleum sulphon'ate's (70% concentration in mineral oil, as in previous compo- The second figure indicates the intensity in which:
0 represents hardly perceptible corrosion. 1 represents slight corrosion. sltions). (i 2 represents heavy corrosion.
ggfig i g I a Each of the four soluble oil compositions whose prepawater ration has been described above was separately tested in the form of their emulsions made from hard water To which is added: (London water), with soft water (Birmingham water), 03 triethanolamine. r and with distilled water, and the results were as follows:
0.3% benzoic acid. H 10% a as as. 1.0% isopropyl alcohol (99%).
Soluble olleontaining Sodium Benzoate. 0.0 1. 1 2.2 Example H golngle 0% cpritaining 'Eriethanolamlne. [1).3 0.0 f A lu l l w p p r having the following s fiiaifiu M23312 1i::::::::::::::: 0:8 3:8 0:0 orm a:
82.5% spindle oil (as used in the previous compositions). t will be s a e compositions p p accord- 13.0% oil-soluble sodium petroleum sulphonates (70% mg to the present invention give hardly perceptible corconcentration in mineral oil, as in previous compo- IOSiOIl Over a fy area flffhe P sitions). The present invention accordingly comprises an mi- 2.5 naphthenic acids. proved soluble oil composition containing a mineral lubri- 0.4% caustic soda. eating oil having a viscosity between 70 and 200 S.S.U.
1.6% water. at 100 R, an emulsifying agent and a minor proportion of triethanolamine benzoate.
To Whlch added: 3 The soluble oil composition may also contain a minor 0.3 triethanolamine. proportion of sodium benzoate as described and claimed 0.2% caustic soda. in British Patent No. 689,740issued July 14, 1950.
0.5% benzoic acid. The present invention also comprises soluble oil emul- 1.0% water, 0 sions formed from 3 to 80 parts by volume of water per 1.0% isopropyl alcohol (99%).
part by volume of the soluble oil composition. h h What we claim is:
of t 6 four cpmposmons mepuoned above.was A soluble oil composition consisting essentially of a sub ected to the COI'I'OSlOIl test standardised by the Institute base stock consisting of about 825% of a miner a1 lubri of Pejtroleum under h number eating oil having a viscosity of about 100 S.S.U. at 100 fi test i castflmn plates of dlmenswns. 4 x 4 X F., about 13% of a 70% oil solution of an oil soluble i a pollshfgg with 0 emery P and were sodium petroleum sulfonate having a molecular weight ceane first wlt acetone and than wlth i f i of approximately 420, about 2.5% of naphthenic acids, on each plate was plaqed grams of Steel mlnmgs and about 0.4% caustic soda and about 1.6% water, and in the plates were placed a test chamber where the addition to said base stock, about 0.3% triethanolamine.
perature was controlled at 650 and the relative about 0.2% caustic soda, about 0.5% benzoic acid and humidity was controlled at 52%. The steel millings on each plate were flooded with 2 mgrn. of prepared emulsions of the appropriate soluble oil compositions, and the plates were left in the test chamber for 24 hours. At the end of this period the steel millings were removed about 1% each of water and isopropyl alcohol.
References Cited in the file of this patent UNITED STATES PATENTS from the plates, and the plates were washed first with 2, Wachiel et 1953 acetone, then with benzene, and were finally gently rubbed 2,668,146 Cafcas et a1. Feb. 2, 1954 with filter paper soaked in benzene. The surfaceof the 2,695,272 King ct a1. Nov. 23, 1954 cast-iron plates were inspected for corrosion, and e ,739,870 Senkus Mar. 27. 1956
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB345960X | 1955-03-29 | ||
GB100256X | 1956-02-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2941944A true US2941944A (en) | 1960-06-21 |
Family
ID=26247181
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US571601A Expired - Lifetime US2941944A (en) | 1955-03-29 | 1956-03-15 | Soluble oil composition |
Country Status (4)
Country | Link |
---|---|
US (1) | US2941944A (en) |
CH (1) | CH345960A (en) |
FR (1) | FR1144852A (en) |
GB (1) | GB788322A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3234252A (en) * | 1962-10-02 | 1966-02-08 | Union Carbide Corp | Siloxane-polyoxyalkylene copolymers |
US3425954A (en) * | 1966-01-24 | 1969-02-04 | Cromwell Paper Co | Four component multipurpose corrosion inhibitor |
US3457173A (en) * | 1962-10-02 | 1969-07-22 | Union Carbide Corp | Aqueous lubricants containing siloxane-polyoxyalkylene compositions |
US3897349A (en) * | 1973-05-29 | 1975-07-29 | Exxon Research Engineering Co | Anti-rust additive composition |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4099915A (en) * | 1977-07-13 | 1978-07-11 | Texaco Inc. | Method for retarding the evaporation of water |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2629649A (en) * | 1949-10-31 | 1953-02-24 | Shell Dev | Vapor-phase corrosion inhibitor |
US2668146A (en) * | 1949-07-23 | 1954-02-02 | Standard Oil Co | Metal-working compositions |
US2695272A (en) * | 1952-05-21 | 1954-11-23 | Standard Oil Dev Co | Soluble metalworking oil |
US2739870A (en) * | 1950-09-15 | 1956-03-27 | Daubert Chemical Co | Composition and sheet material for inhibition of corrosion of metals |
-
1955
- 1955-03-29 GB GB9121/55A patent/GB788322A/en not_active Expired
-
1956
- 1956-03-14 CH CH345960D patent/CH345960A/en unknown
- 1956-03-15 US US571601A patent/US2941944A/en not_active Expired - Lifetime
- 1956-03-27 FR FR1144852D patent/FR1144852A/en not_active Expired
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2668146A (en) * | 1949-07-23 | 1954-02-02 | Standard Oil Co | Metal-working compositions |
US2629649A (en) * | 1949-10-31 | 1953-02-24 | Shell Dev | Vapor-phase corrosion inhibitor |
US2739870A (en) * | 1950-09-15 | 1956-03-27 | Daubert Chemical Co | Composition and sheet material for inhibition of corrosion of metals |
US2695272A (en) * | 1952-05-21 | 1954-11-23 | Standard Oil Dev Co | Soluble metalworking oil |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3234252A (en) * | 1962-10-02 | 1966-02-08 | Union Carbide Corp | Siloxane-polyoxyalkylene copolymers |
US3457173A (en) * | 1962-10-02 | 1969-07-22 | Union Carbide Corp | Aqueous lubricants containing siloxane-polyoxyalkylene compositions |
US3425954A (en) * | 1966-01-24 | 1969-02-04 | Cromwell Paper Co | Four component multipurpose corrosion inhibitor |
US3897349A (en) * | 1973-05-29 | 1975-07-29 | Exxon Research Engineering Co | Anti-rust additive composition |
Also Published As
Publication number | Publication date |
---|---|
CH345960A (en) | 1960-04-30 |
FR1144852A (en) | 1957-10-18 |
GB788322A (en) | 1957-12-23 |
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