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DE1228363B - Organopolysiloxane copolymers as lubricating grease - Google Patents

Organopolysiloxane copolymers as lubricating grease

Info

Publication number
DE1228363B
DE1228363B DEG37976A DEG0037976A DE1228363B DE 1228363 B DE1228363 B DE 1228363B DE G37976 A DEG37976 A DE G37976A DE G0037976 A DEG0037976 A DE G0037976A DE 1228363 B DE1228363 B DE 1228363B
Authority
DE
Germany
Prior art keywords
weight
copolymer
polysiloxane
units
radical
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.)
Pending
Application number
DEG37976A
Other languages
German (de)
Inventor
John Harold Wright
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.)
General Electric Co
Original Assignee
General Electric Co
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 General Electric Co filed Critical General Electric Co
Publication of DE1228363B publication Critical patent/DE1228363B/en
Pending legal-status Critical Current

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    • C08L83/00Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • C08L83/04Polysiloxanes
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    • C10M7/00Solid or semi-solid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single solid or semi-solid substances
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
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    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/12Groups 6 or 16
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/14Group 7
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/16Groups 8, 9, or 10
    • 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
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • 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
    • C10N2050/08Solids
    • 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
    • C10N2050/10Form in which the lubricant is applied to the material being lubricated semi-solid; greasy

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Lubricants (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

BUNDESREPUBLIK DEUTSCHLANDFEDERAL REPUBLIC OF GERMANY

/»Ilk,/ »Ilk,

DEUTSCHES mj9W> PATENTAMTGERMAN mj9W> PATENT OFFICE

AUSLEGESCHRIFTEDITORIAL

Int. Cl.:Int. Cl .:

Nummer:
Aktenzeichen:
Anmeldetag:
Auslegetag:
Number:
File number:
Registration date:
Display day:

ClOmClOm

Deutsche KL: 23 c -1/04 German KL: 23 c - 1/04

1228363
G37976IVc/23c
18.Juni 1963
10. November 1966
1228363
G37976IVc / 23c
June 18, 1963
November 10, 1966

Es ist bekannt, Organopolysiloxane als Schmier-: mittel zu verwenden. Ibxe Konsistenz kann man bekanntlich durch Zusatz^ von organischen und anorga7 rüschen Fettverdickern ändern. Weiterhin ist es be-: reits bekannt, ein Gemisch zweier verschiedener SiI-oxane unter Zusatz von Fettverdickern auf organischer oder anorganischer Basis als Schmiermittel einzusetzen. y .'. ■It is known to use organopolysiloxanes as lubricants. Ibxe consistency can be known to change by the addition of organic and ^ 7 Anorga ruffles grease thickeners. Furthermore, it is already known to use a mixture of two different SiI-oxanes with the addition of fat thickeners on an organic or inorganic basis as a lubricant. y . '. ■

, Schmierfette auf Organopolysiloxanbasis werden häufig auch zum Schmieren von metallischen Teilen verwendet. Zwar werden durch derartige Schmierfette die metallischen Teile selbst nicht angegriffen. Es. hat sich jedoch herausgestellt, daß metallische Teile durch derartige Schmierfette nicht gegen korrodierende Einflüsse in der gewünschten Weise geschützt werden. Dies list besonders bei aus Kupfer, Kupferlegierungen oder Stahl bestehenden Teilen der Fall. Zur Beseitigung !dieses Mangels wurden bisher den Schmierfetten korrosionshemmend wirkende Zusätze einverleibt. Diese Zusätze wirken sich je- ao doch ungünstig auf die Eigenschaften, insbesondere die Wärmebeständigkeit, der Organopolysiloxane aus., Organopolysiloxane-based greases are also often used to lubricate metallic parts used. It is true that the metallic parts themselves are not attacked by such lubricating greases. It. However, it has been found that metallic parts are not protected against corrosion by such lubricating greases Influences are protected in the desired way. This is especially true for those made of copper, Copper alloys or steel existing parts the case. In order to remedy this deficiency, up to now Corrosion-inhibiting additives incorporated into the lubricating grease. These additions each have an effect but unfavorable on the properties, in particular the heat resistance, of the organopolysiloxanes the end.

Es wurde nun gefunden, daß dieser Nachteil nicht eintritt, wenn ein Mischpolymerisat der Formel .It has now been found that this disadvantage does not occur when a copolymer of the formula.

OrganopolysiloxanmischpolymerisateOrganopolysiloxane copolymers

als Schmierfett: as grease :

Anmelder:, ;.Applicant : ,; .

General Electric Company,General Electric Company,

Schenectady, N,Y. (V. St. A.)Schenectady, N, Y. (V. St. A.)

Vertreter:Representative:

Dipl.-Ing. M. Licht, Dr. R. Schmidt,Dipl.-Ing. M. Licht, Dr. R. Schmidt,

Dipl.-Wirtsch.-Ing. A. HansmannDipl.-Wirtsch.-Ing. A. Hansmann

und Dipl.-Phys.S. Herrmann, Patentanwälte,and Dipl.-Phys.S. Herrmann, patent attorneys,

München 2, Theresienstr. 33Munich 2, Theresienstr. 33

Als Erfinder; benannt:As an inventor; named:

John Harold Wright, Waterford, N. Y. (V. St. A.)John Harold Wright, Waterford, N.Y. (V. St. A.)

Beanspruchte Priorität:Claimed priority:

V. St. v. Amerika vom 25. Juni 1962 (205 064) - -V. St. v. America June 25, 1962 (205 064) - -

(R')2(R")SiO —(R ') 2 (R ") SiO -

ΓΗ ■' 1ΓΗ ■ '1
1 ·■ ■1 · ■ ■
—■- ■ RR.
I
Si-O
I
I.
Si-O
I.
bb Si-O
I
Si-O
I.
I ■■■'.···
CH3
I ■■■ '. ···
CH3
I
R
I.
R.

in dex R ein einwertiger, gegebenenfalls halogenierter Kohlenwasserstoff rest oder Cyanalkylrest, R' ein Methyl- oder Phenylres^t, R" ein Methyl-, Phenyl- oder Wasserstoffrest i§t und b mindestens gleich 1, c mindestens gleich 1 und b + c mindestens gleich 10 ist, zusammen mit einem Verdickungsmittel und gegebenenfalls einem Polysiloxan der Formelin dex R a monovalent, optionally halogenated hydrocarbon radical or cyanoalkyl radical, R 'a methyl or phenyl radical, R "a methyl, phenyl or hydrogen radical and b at least equal to 1, c at least equal to 1 and b + c is at least equal to 10, together with a thickener and optionally a polysiloxane of the formula

ν·.·,ν ·. ·, ·...,■■· ..., ■■

' 1R4SiO4 -n
2
' 1 R 4 SiO 4 -n
2

in der R die obige Bedeutung hat und η einen Wert zwischen 2,004 und 2,4 besitzt, wobei der Anteil an Methylwasserstoffpolysiloxaneinheiten imMischpolymerisat 0,1 bis 2 Gewichtsprozent vom Gesamtgewicht an Mischpolymerisat und Polysiloxan beträgt, als Schmierfett verwendet wird.in which R has the above meaning and η has a value between 2.004 and 2.4, the proportion of methyl hydrogen polysiloxane units in the copolymer being 0.1 to 2 percent by weight of the total weight of the copolymer and polysiloxane, is used as the lubricating grease.

Als Polysiloxane verwendet man vorzugsweise solche, in denen wenigstens 50% der siliciumgebundenen organischen Reste Methylreste sind. Ferner bevorzugt man flüssige Polysiloxane, die bei 250C eine Viskosität zwischen etwa 10 und 100 000 cSt aufweisen. Die gegebenenfalls verwendeten flüssigen Organopolysiloxane können gleiche oder verschiedene Siloxaneinheiten von unterschiedlicher Art und Zusammensetzung enthalten, beispielsweise Triorganosiloxan- oder Diorganosiloxaneinheiten allein oder in Verbindung mit Monoorganosiloxaneinheiten.The polysiloxanes used are preferably those in which at least 50% of the silicon-bonded organic radicals are methyl radicals. Liquid polysiloxanes which have a viscosity of between approximately 10 and 100,000 cSt at 25 ° C. are also preferred. The optionally used liquid organopolysiloxanes can contain identical or different siloxane units of different types and compositions, for example triorganosiloxane or diorganosiloxane units alone or in conjunction with monoorganosiloxane units.

Zur Erzielung der erforderlichen Konsistenz können dem Mischpolymerisat die üblichen Verdickungsmittel auf organischer oder anorganischer Basis zugesetzt werden. Beispiele für geeignete Verdickungsmittel sind u. a.die Metallsalze der Fettsäuren mit wenigstens 8 Kohlenstoffatomen.The usual thickeners can be added to the copolymer to achieve the required consistency be added on an organic or inorganic basis. Examples of suitable thickeners include the metal salts of fatty acids with at least 8 carbon atoms.

Obwohl die zugesetzte Menge an Verdickungsr mittel nicht entscheidend ist und in weiten Grenzen variiert werden kann, hat man herausgefunden, daß die Menge gewöhnlich zwischen etwa 2 und 35 Gewichtsprozent, vorzugsweise 2 bis 25 Gewichtsprozent, ausgehend vom Gewicht der Polysiloxane im Fett betragen sollte.Although the amount of thickener added is not decisive and within wide limits can be varied, it has been found that the amount is usually between about 2 and 35 percent by weight, preferably 2 to 25 percent by weight, based on the weight of the polysiloxanes in the Should be fat.

Um eine befriedigende Korrosionsfestigkeit zu erzielen, müssen — bezogen auf das Gewicht des Mischpolymerisats und des Polysiloxans — etwa 0,1 bis 2% Methylwasserstoffsiloxaneinheiten vorhanden sein. Bei weniger als 0,1% Methylwasserstoffpolysiloxaneinheiten wurde eine unzureichende Korrosionsverhütung bei der Berührung mit Kupfer, Kupfer- In order to achieve a satisfactory corrosion resistance, must - based on the weight of the Copolymer and the polysiloxane - about 0.1 to 2% methylhydrogensiloxane units are present be. With less than 0.1% methyl hydrogen polysiloxane units Inadequate corrosion prevention in contact with copper, copper

609 710/272609 710/272

legierungen und Stahl beobachtet. Beträgt der Anteil an Methylwasserstoffpolysiloxaneinheiten über 2 Gewichtsprozent, dann stellte man fest, daß dasMethylwasserstoffpolysiloxan selbst eine Korrosion der Kupfer-, Kupferlegierung- oder Stahlflächen, mit denen das Fett in Berührung gelangt, verursacht.alloys and steel observed. If the proportion of methyl hydrogen polysiloxane units is more than 2 percent by weight, then it was found that the methyl hydrogen polysiloxane itself corrode the Copper, copper alloy or steel surfaces that the grease comes into contact with.

Daher muß das Verhältnis von Methylwasserstoffsiloxaneinheiten in dem flüssigen Mischpolymerisat ursprünglich so gewählt werden, daß die Methylwasserstoffsiloxaneinheiten etwa 0,1 bis 2 Gewichtsprozent des Gesamtgewichts des flüssigen Mischpolymerisats oder, falls ein Polysiloxan vorhanden ist, vom Gesamtgewicht der beiden Komponenten ausmachen. Therefore, the ratio of methylhydrogensiloxane units in the liquid copolymer originally chosen so that the methylhydrogensiloxane units are about 0.1 to 2 percent by weight the total weight of the liquid copolymer or, if a polysiloxane is present, of the total weight of the two components.

Die beanspruchten Schmierfette werden in üblicher Weise durch Mischen hergestellt.The claimed lubricating greases are produced in the usual way by mixing.

Weitere übliche Zusätze können z.B. zur Verbesserung der Schmierfähigkeit und der Beständigkeit der Fette beigegeben werden.Other common additives can be used, for example, to improve lubricity and durability be added to the fats.

Die nachstehenden Ausführungsbeispiele sollen die Durchführung der Erfindung eingehender erläutern. In jedem Fall wurde die Fettmasse durch Vermischen der flüssigen Polysiloxane mit dem Verdickungsmittel in einer Farbmühle bereitet. Die Mischung wurde so lange gemahlen, bis ein gleichförmiges Erzeugnis erhalten wurde. Die Korrosionsfestigkeit jeder Masse wurde durch Auftragen eines Überzuges aus der Masse auf einen, frisch gereinigten, geschmirgelten und polierten Kupferstreifen ermittelt, der nachfolgend in Wasser mit einer Temperatur von 700C getaucht wurde und so lange im Wasser verblieb, bis eine Korrosion zu beobachten war. Die Korrosion zeigte sich dadurch an, daß der Kupferstreifen, verglichen mit dem frischen Kupferstreifen, sich merklich, verfärbt hatte. Wurde ein Kupferstreifen ohne jeglichen Fettüberzug in Wasser getaucht, dann verfärbte er sieh nach 4 Stunden,The following exemplary embodiments are intended to explain the implementation of the invention in more detail. In each case the fat mass was prepared by mixing the liquid polysiloxanes with the thickener in a paint mill. The mixture was milled until a uniform product was obtained. The corrosion resistance of each composition was determined by applying a coating of the composition on a freshly cleaned, sanded and polished copper strip was immersed subsequently in water at a temperature of 70 0 C and as long as remaining in the water was observed to corrosion . The corrosion was indicated by the fact that the copper strip had noticeably discolored compared with the fresh copper strip. If a copper strip was immersed in water without any grease coating, then it discolored after 4 hours,

Beispiel- 1 : Example- 1 :

Ein flüssiges Methylwasserstoffsiloxan-Dimethylsiloxanmischpolymerisat mit durch Trimethylsilyleinheiten gestoppter Kette wurde durch Hydrolysieren und Kondensieren einer Mischung von Methylwasserstofidichlorsilan und Dimethyldichlorsilan und Trimethylchlorsilan in üblicher Weise hergestellt. Die Anteile der verschiedenen Chlorsilane waren so ge^ wählt, daß das entstandene flüssige Polysiloxan 0,5 Gewichtsprozent Methylwasserstoffsiloxan, ausgehend vom Gewicht der Flüssigkeit, enthielt und eine Viskosität von etwa 25'cSt bei 25° C besaß. Dadurch entstand ein Stoff mit einer durch Trimethylsilyl gestoppten Kette, der durchschnittlich ein Mischpolymerisat aus Methylwasserstoffsiloxan- und Dimethylsiloxaneinheiten war. Aus dieser Flüssigkeit bereitete man ein Silikonfett, indem man 10 Gewichtsteile eines feinzerteilten Siliciumdioxyd-Aerogels als Verdickungsmittel mit 100 Teilen der Flüssigkeit mischte. Wurde eine derartige Fettmasse der oben beschriebenen Prüfung auf Korrosionsfestigkeit unter worfen, dann zeigte es sich, daß der Kupferstreifen noch nach Ablauf von 100 Stunden einwandfrei war.A liquid methylhydrogensiloxane / dimethylsiloxane copolymer chain stopped by trimethylsilyl units was obtained by hydrolyzing and condensing a mixture of methylhydrogen dichlorosilane and dimethyldichlorosilane and trimethylchlorosilane prepared in a conventional manner. the The proportions of the various chlorosilanes were similar selects that the resulting liquid polysiloxane is 0.5 percent by weight methylhydrogensiloxane, starting by weight of the liquid, and had a viscosity of about 25'cSt at 25 ° C. Through this a substance was created with a trimethylsilyl stopped Chain, which on average is a copolymer of methylhydrogensiloxane and dimethylsiloxane units was. A silicone grease was prepared from this liquid by adding 10 parts by weight a finely divided silica airgel as a thickener with 100 parts of the liquid mixed. Such a fat mass was subjected to the corrosion resistance test described above then it was found that the copper strip was still flawless after 100 hours had elapsed.

Beispiel 2Example 2

Nach dem Verfahren vom Beispiel 1 wurden Mischpolymerisate ausDimethylsiloxan- undMethylwasserstoffsiloxaneinheiten mit einer durch Trimethylsilyleinheiten gestoppten Kette bereitet, die eine Viskosität von annähernd 25 cSt bei 25° C besaßen und 1,0, 5,0, 10,0 und 20,0 Gewichtsprozent Methylwasserstoffpolysüoxan enthielten. Aus diesen Flüssigkeiten wurden Fette hergestellt, indem man einen Teil jeder Flüssigkeit einem Dimethylpolysiloxan mit durch Trimethylsüyleinheiten gestoppter Kette und einer Viskosität von 300 cSt in der Weise zusetzte, daß ein Gehalt von 0,5 Gewichtsprozent Methylwasserstoffsiloxan, ausgehend vom Gewicht der Flüssigkeiten, erhalten wurde. Jede Fettmasse enthielt IQ Gewichtsprozent, ausgehend vom Gewicht der Flüssigkeiten, eines feinzerteilten Siliciumdioxyd-Aerogels als Verdickungsmittel. Jedes dieser Fette wurde der oben beschriebenen Prüfung auf Korrosionsfestigkeit auf einer Kupferunterlage unterworfen, und jede Probe war nach Ablauf von 100 Stunden noch einwandfrei.Copolymers of dimethylsiloxane and methylhydrogensiloxane units were produced by the method of Example 1 with a chain stopped by trimethylsilyl units which had a viscosity of approximately 25 cSt at 25 ° C and contained 1.0, 5.0, 10.0 and 20.0 weight percent methyl hydrogen polysiloxane. From these Liquids, fats were made by adding a portion of each liquid to a dimethylpolysiloxane with chain stopped by trimethylsulyl units and a viscosity of 300 cSt in the manner added that a content of 0.5 percent by weight methylhydrogensiloxane, based on weight of liquids. Each fat mass contained IQ percent by weight based on weight of liquids, a finely divided silica airgel as a thickener. Each of these Fats were subjected to the above-described test for corrosion resistance on a copper base, and each sample was still flawless after 100 hours.

Claims (1)

Patentanspruch:Claim: Verwendung eines Mischpolymerisats der FormelUse of a copolymer of the formula (R')2(R")SiO-(R ') 2 (R ") SiO- HH —.-. [R 1
I
[R 1
I.
Si-OSi-O Ί
Si-O
1
Ί
Si-O
1
CH3 CH 3 I
R
I.
R.
SifR')2(R")SifR ') 2 (R ") in der R ein einwertiger, gegebenenfalls.halogenierter Kohlenwasserstoffrest oder Cyanalkylrest, R' ein Methyl-.oder Phenylrest, R" ein Methyl-, Phenyl- oder Wasserstöffrest ist und b mindestens gleich 1, c mindestens gleich 1 und b + c mindestens gleich 10 sind, zusammen mit einem Verdickungsmittel und gegebenenfalls einem Polysiloxan der Formelin which R is a monovalent, optionally halogenated hydrocarbon radical or cyanoalkyl radical, R 'is a methyl or phenyl radical, R "is a methyl, phenyl or hydrogen radical and b is at least 1, c is at least 1 and b + c is at least 10 are, together with a thickener and optionally a polysiloxane of the formula R4SiO4-,,R 4 SiO 4 - ,, in der R die obige Bedeutung hat und η einen Wert zwischen 2,004 und 2,4 besitzt, wobei der Anteil an Methylwasserstoffpolysiloxaneinheiten im Mischpolymerisat 0,1 bis 2 Gewichtsprozent vom Gesamtgewicht an Mischpolymerisat und Polysiloxan beträgt, als Schmierfett.in which R has the above meaning and η has a value between 2.004 and 2.4, the proportion of methyl hydrogen polysiloxane units in the copolymer being 0.1 to 2 percent by weight of the total weight of the copolymer and polysiloxane, as a lubricating grease. In Betracht gezogene Druckschriften:
Deutsche Patentschrift Nr. 1170 099.
Considered publications:
German patent specification No. 1170 099.
609 710/272 11.66 © Bundesdruckerei Berlin609 710/272 11.66 © Bundesdruckerei Berlin
DEG37976A 1962-06-25 1963-06-18 Organopolysiloxane copolymers as lubricating grease Pending DE1228363B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US205064A US3145175A (en) 1962-06-25 1962-06-25 Grease composition

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DE1228363B true DE1228363B (en) 1966-11-10

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US (1) US3145175A (en)
DE (1) DE1228363B (en)
GB (1) GB1044536A (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3269949A (en) * 1963-08-30 1966-08-30 Standard Oil Co Grease composition
US3450736A (en) * 1963-09-12 1969-06-17 Mobil Oil Corp Modified siloxane polymers and compositions containing same
NL132928C (en) * 1966-04-14
GB1178906A (en) * 1966-09-15 1970-01-21 Wacker Chemie Gmbh Pastes Based on Organopolysiloxane Oils and Fillers
US4075115A (en) * 1972-09-18 1978-02-21 General Electric Company Silicone fluid useful as a brake fluid
US4005023A (en) * 1973-06-11 1977-01-25 General Electric Company Silicone fluid useful as a brake fluid
US4019997A (en) * 1974-02-04 1977-04-26 General Electric Company Silicone fluid useful as a brae fluid
JPS6020997A (en) * 1983-07-13 1985-02-02 Toshiba Silicone Co Ltd Torque grease
CA1290137C (en) * 1984-06-11 1991-10-08 John L. Burba, Iii Intercalations of crystalline lithium aluminates
JP3541390B2 (en) * 1991-02-22 2004-07-07 東レ・ダウコーニング・シリコーン株式会社 Grease-like silicone composition and method for producing the same
US5162460A (en) * 1991-10-17 1992-11-10 Dow Corning Corporation Moisture-curable silicone corrosion resistant coatings
AU7116798A (en) * 1997-04-16 1998-11-24 University Of Connecticut, The Silicon greases and methods for their production
JP6739951B2 (en) * 2016-03-11 2020-08-12 株式会社デンソー Grease composition, mechanical member and starter overrunning clutch

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Publication number Priority date Publication date Assignee Title
DE1170099B (en) 1960-05-16 1964-05-14 Gen Electric Organopolysiloxane-based lubricating grease

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Publication number Priority date Publication date Assignee Title
US2491843A (en) * 1946-03-21 1949-12-20 Gen Electric Liquid linear methylpolysiloxanes
US2828261A (en) * 1954-02-08 1958-03-25 Standard Oil Co Inorganic gel-thickened lubricant having good temperature susceptibility and dynamicwater stability characteristics
US2945809A (en) * 1954-08-05 1960-07-19 Standard Oil Co Thickened lubricant and process for preparing the same
US2890170A (en) * 1956-09-06 1959-06-09 Dow Corning Organosiloxane greases

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1170099B (en) 1960-05-16 1964-05-14 Gen Electric Organopolysiloxane-based lubricating grease

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US3145175A (en) 1964-08-18
GB1044536A (en) 1966-10-05

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