US2250545A - Lubricating composition - Google Patents
Lubricating composition Download PDFInfo
- Publication number
- US2250545A US2250545A US235778A US23577838A US2250545A US 2250545 A US2250545 A US 2250545A US 235778 A US235778 A US 235778A US 23577838 A US23577838 A US 23577838A US 2250545 A US2250545 A US 2250545A
- Authority
- US
- United States
- Prior art keywords
- xanthogen
- oil
- oils
- lubricating
- sulfur
- 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
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Classifications
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/12—Thio-acids; Thiocyanates; Derivatives thereof
- C10M135/14—Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/14—Synthetic waxes, e.g. polythene waxes
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/16—Paraffin waxes; Petrolatum, e.g. slack wax
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/17—Fisher Tropsch reaction products
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
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- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/022—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
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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
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
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- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
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- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/16—Naphthenic acids
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- C10M2207/10—Carboxylix acids; Neutral salts thereof
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- C10M2207/28—Esters
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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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- C10M2207/40—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
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/082—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type monocarboxylic
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- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/02—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
- C10M2211/022—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aliphatic
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- C10M2211/04—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
- C10M2211/042—Alcohols; Ethers; Aldehydes; Ketones
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- C10M2211/04—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
- C10M2211/044—Acids; Salts or esters thereof
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- C10M2211/06—Perfluorinated compounds
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- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
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- 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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- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/244—Metal working of specific metals
- C10N2040/247—Stainless steel
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Semi-solids; greasy
Definitions
- This invention deals with lubricating composl-1 tions. More specifically, it relates to the use in such compositions of small amounts of soluble organic xanthogen tetrasulfldes which are believed to possess a structure corresponding to the following formula:
- Rand R represent alkyl, cyclic, or-cycloalkyl organic groups.
- Potassium hydroxide is dissolved in absolute a1coho1'(fair excess over that required for reaction) and the required amount of carbon disulflde is added with cooling and mechanical agitation. Potassium xanthate precipitates out. The amount of xanthate is further increased by the addition of ether. excess alcohol being saturated with xanthate could be used again, avoiding the use of ether as a precipitant.) The solid product is recovered by filtration and dried.
- the potassium xanthate is suspended in benzene (other inert solvents such as light naphtha could be used), stirred and a benzene solution of sulfur monochloride added with cooling. After the sulfur chloride has been added, the reaction mixture is refluxed for 2 hours to complete the condensation, and then poured into water. The benzene layer is removed and dried. After stripping off the benzene, the xanthogen tetrasulflde remains as a residue.
- benzene other inert solvents such as light naphtha could be used
- 'I'hese compounds are also compatible with soap, fatty oils and other ingredients normally employed in soluble oils, cutting oils, greases, motor oils, compounded, and industrial lubricants, without causing precipitation. or settling out of sulfur or sulfur compounds.
- the xanthogen tetrasulfides e. g. ethyl xanthogen tetrasulflde
- 3% of this material will carry the full load (580 lbs.) on the S. A. E. machine at 1000 R. P. M., and in addition, it meets the requirements of the Packard Stability Test.
- This test involves the heating of the blend in an oven at 200 F. for 64 hrs. and running the thus-treated oil on the S. A. E. machine at 1000 R. P. M. and 83.6 lbs/sec. loading rate, the rubbing ratio being 14.6:1.
- the blend must carry a full load of 550 lbs. scale pull.
- Blends containing these xanthogen tetrasulxanthate salt prior to condensation Since these products pick up some of the mercaptan odor which is dimcult to remove, they are not as desirable as the corresponding alcohol derivatives.
- compositions which are the subject of this invention are in the field of cutting oils.
- a high E. P. eflect is desired without any detrimental odor or discoloration oi! the base stock, so as to give clean work pieces without need for further handling or processing.
- Soluble cut ting oils are prepared by the addition of emulsihere such as sodium naphthenate, mahogany 1 in which the tetrasuliide is an alkyl xanthogen tetrasulilde.
- a cutting oil comprising a mineral lubricating oil and about 2 to% oia soluble xanthogen tetrasulfide having the probable structure:
- R and R are alkyl, cyclic or cyclo-alkyl groups, and the oxygen atoms may be replaced by sulfur.
- the lubricating oil base stocks are generally crude or refined mineral oils of about 70 viscosity at 100 F. (Saybolt) to about 5000 viscosity at 100 F.
- compositions may be employed i conjunction with linear polymer V.
- linear polymer V. I. improvers, pour inhibitors, dyes, resins, voltolized'iats and/ or mineral oils or waxes, ester and other oiliness agents, phenolic or amino oxidation inhibitors, soaps, such as calcium stearate, lead oleate, lead naphthenate, aluminum naphthenate, and the like, dyes, halogenated compounds, such aschlorinated esters, chlorinated parailin waxes, etc., wetting agents, insecticides, germicides, fungicides, and the like.
- composition of matter comprising any oil selected from the group consisting oi mineral oils and fatty oils, and a small amount of organic xanthogen tetrasulfide.
- a lubricating composition comprising a lubricating oil base stock and at least about .01% of a soluble xanthogen sulfide having the general formula:
- n-x-ti-(s)l-ii-x a where R and R are like or unlike alkyl, cyclic hydrocarbon, or mixed cyclo-alkyl radicals,'and X is either oxygen or sulfur.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Patented July 29, 194i LUBRIYCATING COMPOSITION Louis A. Mikeska, Westiield, and Eugene liieber,
Linden, N. J., assignors to Standard Oil Development Company, a corporation of Delaware No Drawing. Application October 19,1938,
sci-a1 No. 235,771;
3 Claims. (Cl. 252-46) This invention deals with lubricating composl-1 tions. More specifically, it relates to the use in such compositions of small amounts of soluble organic xanthogen tetrasulfldes which are believed to possess a structure corresponding to the following formula:
where Rand R. represent alkyl, cyclic, or-cycloalkyl organic groups.
These compounds are condensation products which may be obtained in high yields according to the following reactions:
. Z3 ROH+CS:+KOH R-0-C +1110 Potassium xanthate Xsnthogen tetrasulflde An example in the preparation of such a material (ethyl xanthogen tetrasulfide) is as follows:
Potassium hydroxide is dissolved in absolute a1coho1'(fair excess over that required for reaction) and the required amount of carbon disulflde is added with cooling and mechanical agitation. Potassium xanthate precipitates out. The amount of xanthate is further increased by the addition of ether. excess alcohol being saturated with xanthate could be used again, avoiding the use of ether as a precipitant.) The solid product is recovered by filtration and dried.
The potassium xanthate is suspended in benzene (other inert solvents such as light naphtha could be used), stirred and a benzene solution of sulfur monochloride added with cooling. After the sulfur chloride has been added, the reaction mixture is refluxed for 2 hours to complete the condensation, and then poured into water. The benzene layer is removed and dried. After stripping off the benzene, the xanthogen tetrasulflde remains as a residue.
The overall yield averages around 86.7%.
These xanthogen tetrasulfldes possess such un- (In large production, the
and corrosion inhibiting properties. They likewise .exhibit exceptionally potentextreme pressure lubricating properties. Although they are sulfur compounds (ethyl xanthogen tetrasulfide contains about 63% S), they are light colored, oil soluble compounds, possessing a faint pleasant odor, and thus impart no objectionable characteristics to the mineral or other oil base stockin which they are blended.
'I'hese compounds are also compatible with soap, fatty oils and other ingredients normally employed in soluble oils, cutting oils, greases, motor oils, compounded, and industrial lubricants, without causing precipitation. or settling out of sulfur or sulfur compounds.
In the extreme pressure lubricating art the common practice is to add to the lubricating 'oil a sulfurized mineral or fatty 'oil. These com- .pounds are generally dark colored, odorous materials, poor in combined sulfur. Alkyl sulfides and polysulfides have been proposed for this purpose but their pungent and sickening odor markedly limits their uses in this direction. Xanthogen disulfldes, prepared by the oxidation of xanthic salts show relatively poor load carryirig properties, a 5% blend failing on the S. A. E
machine at 200 lbs. load. Although ethyl xanusual characteristics as to impart to lubricating and other oils, new and unexpected properties. For example, they possess excellent antioxidant thogen'trisulfide shows fair load carrying properties, it tends to settle out free sulfur on standing, and is therefore excluded from use to some extent because of its instability. An improved composition can be obtained by chilling the trisulflde or its solutions and filtering to remove the separated material.
However, the xanthogen tetrasulfides (e. g. ethyl xanthogen tetrasulflde) such as'those embodied in the present invention, give excellent results as extreme pressure blending agents. When used alone in mineral lubricating oil, 3% of this material will carry the full load (580 lbs.) on the S. A. E. machine at 1000 R. P. M., and in addition, it meets the requirements of the Packard Stability Test. This test involves the heating of the blend in an oven at 200 F. for 64 hrs. and running the thus-treated oil on the S. A. E. machine at 1000 R. P. M. and 83.6 lbs/sec. loading rate, the rubbing ratio being 14.6:1. The blend must carry a full load of 550 lbs. scale pull.
Blends containing these xanthogen tetrasulxanthate salt prior to condensation. Since these products pick up some of the mercaptan odor which is dimcult to remove, they are not as desirable as the corresponding alcohol derivatives.
One exceptionally wide use for the compositions which are the subject of this invention, is in the field of cutting oils. Here a high E. P. eflect is desired without any detrimental odor or discoloration oi! the base stock, so as to give clean work pieces without need for further handling or processing. For this purpose, it is desired to employ about 2 to 10% of the tetrasulfide condensation products previously described. Soluble cut ting oils are prepared by the addition of emulsihere such as sodium naphthenate, mahogany 1 in which the tetrasuliide is an alkyl xanthogen tetrasulilde.
3. A lubricating composition according to claim 1 in which the tetrasulflde is ethyl xanthyl tetrasulilde.
4. A lubricating composition according to claim i in which the mineral oil is an oil oi. high viscosity index. j
5. A cutting oil comprising a mineral lubricating oil and about 2 to% oia soluble xanthogen tetrasulfide having the probable structure:
where R and R are alkyl, cyclic or cyclo-alkyl groups, and the oxygen atoms may be replaced by sulfur.
soaps, rosin soaps, glycerol, alcohol and similar ingredients. 1 The lubricating oil base stocks are generally crude or refined mineral oils of about 70 viscosity at 100 F. (Saybolt) to about 5000 viscosity at 100 F.
In many cases, where antioxidant and anticorrosion effects are more desired, about 0.01 to 2% of the xanthate tetrasulildes is sumcient. For the preparation or E. P. greases and gear oils, higher viscosity base stocks may be employed, and there is often an advantage to employ stocks of high viscosity index, e. g. above 50. v
The present compositions may be employed i conjunction with linear polymer V. I. improvers, pour inhibitors, dyes, resins, voltolized'iats and/ or mineral oils or waxes, ester and other oiliness agents, phenolic or amino oxidation inhibitors, soaps, such as calcium stearate, lead oleate, lead naphthenate, aluminum naphthenate, and the like, dyes, halogenated compounds, such aschlorinated esters, chlorinated parailin waxes, etc., wetting agents, insecticides, germicides, fungicides, and the like.
The invention is not limited to any theory or structure or action, but islimited only by the 6. A composition of matter comprising any oil selected from the group consisting oi mineral oils and fatty oils, and a small amount of organic xanthogen tetrasulfide.
7. A lubricating composition comprising a lubricating oil base stock and at least about .01% of a soluble xanthogen sulfide having the general formula:
n-x-ti-(s)l-ii-x a where R and R are like or unlike alkyl, cyclic hydrocarbon, or mixed cyclo-alkyl radicals,'and X is either oxygen or sulfur.
8. The method of preparing improved lubrieating compositions which comprises reacting a compound having the general formula R--XH where R is an alkyl, cyclic hydrocarbon,-or mixed cyclo-alkyl radical and X is either oxygen or sulfur, with carbon disuliide and with a metal hydroxide to form a xanthate having the general formula:
I where M represents the nietal, then reacting 2 claims in which it is the intention to cover the s DISCLAIMER- mols or such xanthate in whichthe R constitu- -2,250,545ritual A. Mantra, Westfield, and' Eugene Lieber, Linden, N. .1. Lunaros'rma Courosrrrou. 'Patent dated July' 29, 1941. Disclaimer. filed 4 April 14, 1942, by the assignee, StandardOtl Development Company. Hereby enters this disclaimer to claims 1, 2, 3, 6, and 7.
[Oficial Gazette June 2, 1942.]
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL51053D NL51053C (en) | 1938-10-19 | ||
US235778A US2250545A (en) | 1938-10-19 | 1938-10-19 | Lubricating composition |
GB13059/39A GB522189A (en) | 1938-10-19 | 1939-05-02 | Improved lubricating compositions |
FR855166D FR855166A (en) | 1938-10-19 | 1939-05-23 | Lubricant |
DEST59124D DE710095C (en) | 1938-10-19 | 1939-09-27 | Mineral lubricating oils |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US235778A US2250545A (en) | 1938-10-19 | 1938-10-19 | Lubricating composition |
Publications (1)
Publication Number | Publication Date |
---|---|
US2250545A true US2250545A (en) | 1941-07-29 |
Family
ID=22886869
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US235778A Expired - Lifetime US2250545A (en) | 1938-10-19 | 1938-10-19 | Lubricating composition |
Country Status (5)
Country | Link |
---|---|
US (1) | US2250545A (en) |
DE (1) | DE710095C (en) |
FR (1) | FR855166A (en) |
GB (1) | GB522189A (en) |
NL (1) | NL51053C (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2431010A (en) * | 1941-07-19 | 1947-11-18 | Standard Oil Dev Co | Soluble cutting oil |
US2498863A (en) * | 1945-08-30 | 1950-02-28 | Socony Vacuum Oil Co Inc | Lubricating oil composition |
US2574457A (en) * | 1947-08-05 | 1951-11-13 | Phillips Petroleum Co | Manufacture of alkyl sulfenyl trithiocarbonates |
US2615804A (en) * | 1947-05-08 | 1952-10-28 | Goodrich Co B F | Herbicidal composition |
US2615802A (en) * | 1948-10-23 | 1952-10-28 | Monsanto Chemicals | Herbicidal composition and method |
US2743209A (en) * | 1952-12-24 | 1956-04-24 | Robert H Jones | Xanthyl and trithiocarbonyl, sulfides, sulfoxides, and sulfones as pesticides |
US2743210A (en) * | 1952-12-24 | 1956-04-24 | Stauffer Chemical Co | Xanthogen and dtthiocarbonyl tetrasulfides as pesticides |
US2813890A (en) * | 1954-10-15 | 1957-11-19 | Exxon Research Engineering Co | Manufacture of alkyl xanthogen sulfides |
US2925386A (en) * | 1952-08-25 | 1960-02-16 | Huels Chemische Werke Ag | Mineral oil base lubricant |
US3864374A (en) * | 1973-11-19 | 1975-02-04 | Canadian Ind | Manufacture of alkali metal xanthates |
-
0
- NL NL51053D patent/NL51053C/xx active
-
1938
- 1938-10-19 US US235778A patent/US2250545A/en not_active Expired - Lifetime
-
1939
- 1939-05-02 GB GB13059/39A patent/GB522189A/en not_active Expired
- 1939-05-23 FR FR855166D patent/FR855166A/en not_active Expired
- 1939-09-27 DE DEST59124D patent/DE710095C/en not_active Expired
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2431010A (en) * | 1941-07-19 | 1947-11-18 | Standard Oil Dev Co | Soluble cutting oil |
US2498863A (en) * | 1945-08-30 | 1950-02-28 | Socony Vacuum Oil Co Inc | Lubricating oil composition |
US2615804A (en) * | 1947-05-08 | 1952-10-28 | Goodrich Co B F | Herbicidal composition |
US2574457A (en) * | 1947-08-05 | 1951-11-13 | Phillips Petroleum Co | Manufacture of alkyl sulfenyl trithiocarbonates |
US2615802A (en) * | 1948-10-23 | 1952-10-28 | Monsanto Chemicals | Herbicidal composition and method |
US2925386A (en) * | 1952-08-25 | 1960-02-16 | Huels Chemische Werke Ag | Mineral oil base lubricant |
US2743209A (en) * | 1952-12-24 | 1956-04-24 | Robert H Jones | Xanthyl and trithiocarbonyl, sulfides, sulfoxides, and sulfones as pesticides |
US2743210A (en) * | 1952-12-24 | 1956-04-24 | Stauffer Chemical Co | Xanthogen and dtthiocarbonyl tetrasulfides as pesticides |
US2813890A (en) * | 1954-10-15 | 1957-11-19 | Exxon Research Engineering Co | Manufacture of alkyl xanthogen sulfides |
US3864374A (en) * | 1973-11-19 | 1975-02-04 | Canadian Ind | Manufacture of alkali metal xanthates |
Also Published As
Publication number | Publication date |
---|---|
GB522189A (en) | 1940-06-11 |
NL51053C (en) | |
FR855166A (en) | 1940-05-04 |
DE710095C (en) | 1941-09-03 |
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