DE1257331B - Waessrige Metallbearbeitungsfluessigkeit - Google Patents

Waessrige Metallbearbeitungsfluessigkeit

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Publication number
DE1257331B
DE1257331B DES91029A DES0091029A DE1257331B DE 1257331 B DE1257331 B DE 1257331B DE S91029 A DES91029 A DE S91029A DE S0091029 A DES0091029 A DE S0091029A DE 1257331 B DE1257331 B DE 1257331B
Authority
DE
Germany
Prior art keywords
anhydride
acid
weight
percent
succinic
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
DES91029A
Other languages
English (en)
Inventor
Robert Hall Davis
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.)
ExxonMobil Oil Corp
Original Assignee
Mobil Oil Corp
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 Mobil Oil Corp filed Critical Mobil Oil Corp
Publication of DE1257331B publication Critical patent/DE1257331B/de
Pending legal-status Critical Current

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    • C10M2219/09Heterocyclic compounds containing no sulfur, selenium or tellurium compounds in the ring
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/102Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon only in the ring
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • C10M2219/106Thiadiazoles
    • 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
    • C10M2227/00Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
    • C10M2227/09Complexes with metals
    • 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
    • C10N2010/02Groups 1 or 11
    • 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
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/12Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
    • 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
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/01Emulsions, colloids, or micelles

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Description

BUNDESREPUBLIK DEUTSCHLAND
Int. Cl.:.
ClOm
DEUTSCHES
PATENTAMT
PATENTSCHRIFT
Deutsche Kl.: 23 c-1/04
Nummer:
Aktenzeichen:
Anmeldetag:
1257 331.
S91029IVc/23c
12. Mai 1964
28. Dezember 1967
4. Juli 1968
Auslegetag:
Ausgabetag:
Patentschrift stimmt mit der Auslegeschrift überein
Wäßrige Metallbearbeitungsflüssigkeiten sind bereits bekannt.
Zu den Anforderungen an solche Metallbearbeitungsfiüssigkeiten gehören korrosionshemmende Eigenschaften für eisenhaltige und kupferhaltige Legierungen sowie Beständigkeit unter den Arbeitsbedingungen. Weiterhin dürfen sich nach der Metallbearbeitung keine Rückstände auf dem Werkzeug und dem Werkstück ergeben. Weitere Anforderungen sind: Vermeidung einer übermäßigen Schaumbildung, ίο Beständigkeit gegen Ranzigwerden und Verwendbarkeit in Lösungen mit hartem Wasser, so daß keine Ausfällung von Bestandteilen eintritt. Die bisher bekannten Mittel haben jedoch nicht alle vorstehend aufgeführten Anforderungen in zufriedenstellender Weise erfüllt. ,
Es wurde nun gefunden, daß diese Eigenschaften durch eine Metallbearbeitungsflüssigkeit erzielt werden, welche eine Kombination von drei je einzeln als Schmierölzusätze bekannten Komponenten, nämlich 5 bis 40 Gewichtsprozent eines Alkanolamine, 0,1 bis 9 Gewichtsprozent einer Carbonsäure mit 6 bis 12 Kohlenstoffatomen und 0,1 bis 9 Gewichtsprozent einer Alkenylbernsteinsäure bzw. deren Anhydrid, wobei der Alkenylrest gerad- oder verzweigtkettig oder durch Wasserstoff, Schwefel oder Halogen substituiert sein kann, enthält.
Als Alkanolamine.werden solche, wie Mono-, Dioder Triäthanolamin oder Isopropandlamine und Methyldiäthanolamin oder auch Gemische derselben verwendet.
Als Säuren werden solche mit mittlerem Molekulargewicht, nämlich .mit 6 bis 12 Kohlenstoffatomen je Molekül verwendet. Es können gesättigte oder ungesättigte Säuren oder Mischungen sein. Bevorzugt sind Säuren mittleren Molekulargewichts, wie önanthsäure, Caprylsäure, Caprinsäure, Pelargonsäure, Capronsäure, Undecylensäure, Undecylsäure und Laurinsäure.
Als Alkenylbernsteinsäureanhydrid bzw. Säure werden solche der Formeln
R — CH- c;
CH,-C;
Anhydrid
',O
:O
>0
>o
R-- CH- c:
OH
CH? C
Säure
worin R ein geradkettiger oder verzweigtkettiger Alkenylrest sein kann ■'■ uch durch Schwefel oder Wäßrige Metallbearbeitungsflüssigkeit
Patentiert für: ,«
Mobil Oil Corporation, *
New York, N. Y. (V. St. A.)
Vertreter:
Dr. E. Wiegand
und Dipl.-Ing. W. Niemann, Patentanwälte,
München 15, Nußbaumstr. 10
Als Erfinder benannt:
Robert Hall Davis, Pitman, N. J. (V. St. A.)
Beanspruchte Priorität:
V. St. v. Amerika vom 17. Mai 1963 (281 351) — \
Halogen substituiert sein kann, verwendet. Der Alkenylrest enthält mindestens zwei Kohlenstoffatome. Beispiele sind: Äthenylbernsteinsäureanhydrid, Äthenylbernsteinsäure, Äthylbernsteinsäureanhydrid, Propenylbernsteinsäureanhydrid, sulfuriertes Propenylbernsteinsäureanhydrid, Butenylbernsteinsäure, 2 - Methylbutenylbernsteinsäureanhydrid, 1,2-Dichlorpentylbernsteinsäureanhydrid, Hexenylbernsteinsäureanhydrid, Hexylbernsteinsäure, sulfuriertes 3 - Methylpentenylbernsteinsäureanhydrid, 2,3-Dimethylbutenylbernsteinsäureanhydrid, 3,3-Dimethylbutenylbernsteinsäure, 1,2-Dibrom-2-äthylbutylbernsteirisäure, Heptenylbernsteinsäureanhydrid, 1,2-Dijodoctylbernsteinsäure, Octenylbernsteinsäureanhydrid, Diisobutenylbernsteinsäureanhydrid, 2-Methylheptenylbernsteinsäureanhydrid, 4-Äthylhexenylbernsteinsäure, 2-Isopropylpentenylbernsteinsäureanhydrid, Nonenylbernsteinsäureanhydrid, 2 - Propylhexenylbernsteinsäureanhydrid, Decenylbernsteinsäure, Decenylbernsteinsäureanhydrid,
5-Methyl-2-isopropylhexenylbernsteinsäureanhydrid, 1,2 - Dibrom - 2 - äthyloctenylbernsteinsäureanhydrid, Decylbernsteinsäureanhydrid, Undecenylbernsteinsäureanhydrid, 1,2 - Dichlorundecylbernsteinsäüre, S-Äthyl-i-tert.-butylpentenylbernsteinsäureanhydrid, Tctrapropenyl bernsteinsäureanhydrid, Tetrapropenylbernsteinsäure, Triisobutenylbernsteinsäureanhydrid, 2-Propyl-nonenylbernsteinsäureanhydrid, 3-Butyloctcnylbernstcinsäureanhydrid, Tridecenylbern-
809 583,88
steinsäureanhydrid, Tetradecenylbernsteinsäureanhydrid, Hexadecenylbernsteinsäureanhydrid, sulfurierte Octadecenylbernsteinsäure, Octadecylbernsteinsäureanhydrid, 1 ^-Dibrom^-methylpentadecenylbernsteinsäureanhydrid, 8 - Pröpylpentadecylbemsteinsäureanhydrid, Eicosenylbernsteinsäureanhydrid, 1,2 - Dichlor - 2 - methylnonadecenylbernsteinsäureanhydrid, 2 - Octyldodecenylbernsteinsäure, 1,2-Dijodtetracosenylbernsteinsäureanhydrid, Hexacosenylbernsteinsäure, Hexacosenylbernsteinsäureanhydrid und Hentriacontenylbernsteinsäureanhydrid.
Die Verfahren zur Herstellung der Alkenylbernsteinsäureanhydride sind bekannt. Ein geeignetes Verfahren bedient sich der Reaktion eines Olefins mit Maleinsäureanhydrid.
Alkenylbernsteinsäuren bzw. deren Anhydride mit 8 bis 12 Kohlenstoffatomen je Molekül werden bevorzugt. Weiter können andere übliche Zusätze beigegeben werden, z. B. Alkalinitrite oder Natriumsalze von Mercaptobenzothiazol, Phenole, wie Natriumsalze von Orthophenylphenol, chlorierten Phenolen, oder Borsäure und Boroxyde oder Alkalihydroxyd oder Chelatbildungsmittel, wie das Natriumsalz von D'iäthylentriaminpentaessigsäure 'oder Salze von Äthylendiamintetraessigsäure oder Nitrilotriessigsäure.
Die Mengenverhältnisse der Kombination sind: Alkanolamin 5 bis 40 Gewichtsprozent, vorzugsweise 20 bis 35 Gewichtsprozent, die Säure 0,1 bis 9 Gewichtsprozent, vorzugsweise 1 bis 4 Gewichtsprozent, die Alkenylbernsteinsäure bzw. deren Anhydrid' 0,1 bis 9 Gewichtsprozent, vorzugsweise 0,1 bis 4 Gewichtsprozent. .
' Die Metallbearbeitungsflüssigkeit wird wie üblich durch einfaches Mischen der Komponenten mit 10 bis 20 Teilen Wasser hergestellt. Anschließend kann weiteres Wasser zugegeben werden.
Die verbesserten Eigenschaften der beanspruchten Kombination bei Vergleich mit den Einzelkomponenten sind aus den nachfolgenden Beispielen ersichtlich.
Korrosionstest
Schmiedeeisenstückchen wurden in einen 50-ml-Becher eingebracht, zusammen mit dem zu untersuchenden Medium. Dann wurde alle überschüssige Flüssigkeit abgegossen, und der Becher wurde in einer Atmosphäre mit einer relativen Feuchtigkeit von etwa 90% bei einer Temperatur von etwa 21 bis 24° C abgestellt. Nach einem Lagerzeitraum von 48 Stunden wurde die Probe dann auf das Auftreten von Rost geprüft.
Wirksamkeit bei maschinellen
Bearbeitungsvorgängen
Die Wirksamkeit bei maschinellen Bearbeitungsvorgängen wurde in Verbindung mit einer Reihe von Löchern, die in einen Prüfstab aus heiß gewalztem Stahl gebohrt waren und in die ein Gewinde einzuschneiden war, festgestellt. Vor der Prüfung wurden Proben unter Verwendung von 1 Gewichtsteil des Additivkonzentrats auf 5 Gewichtsteile destilliertes Wasser verdünnt. Die Flüssigkeit wurde dem Gewindebohrloch mit einer Polyäthylenquetschflasche zugeführt. Vier unbekannte Proben waren von zwei Standardproben umschlossen und wurden mit diesen verglichen. Die Gewindebohrwirksamkeit wurde berechnet, indem die bei den unbekannten Proben ermittelte Drehkraft durch die mittlere Drehkraft bei den Standardproben geteilt und mit 100 multipliziert wurde.
Triäthanolamin
Gewichtsprozent
Caprylsäure
Gewichtsprozent
Tabelle I Destilliertes Wasser
Gewichtsprozent
Schmiedeeisentest*)
Beispiel 24
24
24
6
3
Nonenylbernsteinsäure-
anhydrid
Gewichtsprozent
70
70
70
Rost
Rost
kein Rost
1
2
3
OJ On I
*) Bei diesem Test werden Schmiedeeisenteilchen während 48 Stunden in eine Lösung von 1 Teil Rostinhibitor und 40 Teilen Wasser eingebracht.
Aus dem Beispiel 3 ist eine deutliche synergistische Wirkung der beanspruchten Kombination ersichtlich.
Tabelle!! ,
Beispiel Triäthanolamin
Gewichtsprozent
Caprylsäure
Gewichtsprozent
Nonenylbernstein-
säureanhydrid
Gewichtsprozent
Destilliertes Wasser
Gewichtsprozent
Gewindebohrwirksamkeit,
1 bis 5 Verdünnung der
Grundzusammensetzung
mit destilliertem Wasser*)
4
5
6
30
20
20
10
3
7 O ο O 75,7
81,7
94,7
*) In bezug auf ein Vergleichsschneidmedium, wie es in der USA.-Patentschrift 3 071 545 beschrieben ist; die Ergebnisse stellen das Mittel aus zwei Prüfungen dar.

Claims (1)

  1. Patentanspruch:
    Wäßrige Metallbearbeitungsflüssigkeit, enthaltend drei je einzeln als Schmierölzusätze bekannte Komponenten und gegebenenfalls andere übliche Zusätze, dadurch gekennzeichnet, daß sie 5 bis 40 Gewichtsprozent eines Alkanolamine, 0,1 bis 9 Gewichtsprozent einer Carbonsäure mit 6 bis 12 Kohlenstoffatomen und 0,1 bis 9 Gewichtsprozent einer Alkenylbernsteinsäure · bzw. deren Anhydrid, wobei der Alkenylrest gerad- oder verzweigtkettig oder durch Wasserstoff, Schwefel oder Halogen substituiert sein kann, enthält.
    709 710/534 12.67 © Bundesdruckerei Berlin
DES91029A 1963-05-17 1964-05-12 Waessrige Metallbearbeitungsfluessigkeit Pending DE1257331B (de)

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US (1) US3256187A (de)
AT (1) AT249839B (de)
CH (1) CH482825A (de)
DE (2) DE1257331B (de)
FR (2) FR1392444A (de)
GB (2) GB1028458A (de)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3897351A (en) * 1973-10-04 1975-07-29 Mobil Oil Corp Lubricant compositions
US4519925A (en) * 1976-04-28 1985-05-28 The Lubrizol Corporation Sulfur-containing compounds and lubricants containing them
US4129510A (en) * 1976-04-28 1978-12-12 The Lubrizol Corporation Sulfur-containing compounds and lubricants and fuels containing them
FR2364266A1 (fr) * 1976-09-13 1978-04-07 Mobil Oil Compositions lubrifiantes perfectionnees contenant des sels d'esters partiels d'acides alkyl- ou alcenylsucciniques
US4239636A (en) * 1978-10-23 1980-12-16 Exxon Research & Engineering Co. Thio-bis-(alkyl lactone acid esters) and thio-bis-(hydrocarbyl diacid esters) are useful additives for lubricating compositions
US4146488A (en) * 1978-01-24 1979-03-27 Union Carbide Corporation Metal lubricants
US4289636A (en) * 1979-10-01 1981-09-15 Mobil Oil Corporation Aqueous lubricant compositions
US4425248A (en) 1981-12-18 1984-01-10 Mobil Oil Corporation Water soluble lubricant compositions
US4725373A (en) * 1986-02-24 1988-02-16 The Dow Chemical Company Novel compositions prepared from alkyl substituted nitrogen-containing aromatic heterocyclic compounds and dicarboxylic acid monoanhydrides
US4670168A (en) * 1986-05-01 1987-06-02 Aluminum Company Of America Aqueous metal removal fluid
US4900358A (en) * 1988-03-30 1990-02-13 King Industries, Inc. Water soluble corrosion inhibiting compositions and protective coatings prepared therefrom
DE10046265A1 (de) * 2000-09-19 2002-03-28 Bayer Ag Wirkstoffkombination zum Schutz von tierischen Häuten
DE102007033430A1 (de) * 2007-07-18 2009-01-22 Evonik Goldschmidt Gmbh Siliconfreies Schneidöl und seine Verwendung

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2638449A (en) * 1949-12-30 1953-05-12 Socony Vacuum Oil Co Inc Reaction products of fatty acids, dialkanolamines, and alkenyl succinic acid anhydrides
NL86209C (de) * 1952-03-08
US2825693A (en) * 1955-02-03 1958-03-04 Shell Dev Metal working lubricant
DE1033825B (de) * 1957-01-31 1958-07-10 Hamker & Rieth Verfahren zur Herstellung von transparentwasserloeslichen Metallbearbeitungs- und Kuehlkonzentraten
BE596639A (de) * 1960-02-08

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FR1392444A (fr) 1965-03-12
GB1028458A (en) 1966-05-04
AT249839B (de) 1966-10-10
CH482825A (de) 1969-12-15
GB1021004A (en) 1966-02-23
FR1393172A (fr) 1965-03-19
DE1284018B (de) 1968-11-28

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