US2016201001A1PendingUtilityA1
Additive for oil-based lubricants having improved extreme pressure properties
Est. expiryAug 21, 2033(~7.1 yrs left)· nominal 20-yr term from priority
Inventors:Helmut Fackler
C10N 2040/08C10M 2207/021C10N 2040/135C10N 2030/40C10M 2215/223C10N 2040/20C10N 2040/50C10N 2040/06C10N 2040/02C10N 2030/62C10N 2040/16C10N 2040/243C10N 2030/70C10N 2050/10C10N 2040/30C10M 2215/04C10M 2209/105C10N 2040/25C10N 2040/04C10M 2219/106C10N 2030/12C10M 2207/022C10N 2030/06C10M 2203/024C10N 2040/22C10M 2207/40C10M 141/08C10M 2207/023C10N 2040/24C10M 2223/042C10M 2209/107C10M 2215/28C10M 2207/289C10M 133/06C10M 135/36C10M 127/02
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Claims
Abstract
The present invention relates to a novel additive for oil-based lubricants having improved extreme-pressure properties, to a method for producing said novel additive, to oil-based lubricants containing said novel additive and to uses of said novel additive.
Claims
exact text as granted — not AI-modified1 . A process for producing a lubricant additive, wherein
a)
i) a dimeric thiadiazole compound, especially a bis(2-alkyl-1,3,4-thiadiazolyl) 5,5′-disulfide derivative of the formula (I)
and/or a dimeric 2,5-dimercapto-1,3,4-thiadiazolethiol derivative of the formula (II)
where n in the formulae (I) and (II) is 1 or 2 and
R1 and R2 are each independently hydrogen, linear or branched alkyl groups having 1 to 12 carbon atoms, especially thioalkyl groups having 1 to 12 carbon atoms, aromatic radicals or heteroaromatic radicals,
ii) is dissolved in a polyamine or polyamine derivative of the formula (III)
R1-(CH2-CH2-NH) n -CH2-CH2-R2 (III)
where n in formula (III) is an integer from 1 to 15, especially an integer from 3 to 8, and
R1 and R2 are each independently hydrogen, —NH2, linear or branched alkyl groups having 1 to 12 carbon atoms or a modified or unmodified succinimide group, and
iii) a compound of the formula (IV)
in which n is an integer from 1 to 8, especially an integer from 3 to 8, preferably 6, is added to the solution obtained,
or
b)
i) a dimeric thiadiazole compound, especially a bis(2-alkyl-1,3,4-thiadiazolyl) 5,5′-disulfide derivative of the formula (I)
and/or a dimeric 2,5-dimercapto-1,3,4-thiadiazolethiol derivative of the formula (II)
where n in the formulae (I) and (II) is 1 or 2 and
R1 and R2 are each independently hydrogen, linear or branched alkyl groups having 1 to 12 carbon atoms, especially thioalkyl groups (—SR) having 1 to 12 carbon atoms, aromatic radicals or heteroaromatic radicals,
ii) is dissolved in a polyol, especially a polyether polyol having a high propylene oxide content and/or a triglyceride having a hydroxy fatty acid component, and
iii) a hydrophobic phenol derivative and/or unsaturated fatty alcohol is added to the solution obtained.
2 . The process as claimed in claim 1 , wherein
in alternative a), the dimeric thiadiazole compound used is 5,5′-dithiobis(1,3,5-thiadiazole-2-thiol), and/or in alternative a), the polyamine or polyamine derivative of the formula (III) used is the mono-succinimide derivative of the formula (V) or the bissuccinimide derivative of the formula (VI), and/or in alternative a), the compound of the formula (IV) used is farnesene, lycopene or squalene.
3 . The process as claimed in claim 1 , wherein
in alternative b), the dimeric thiadiazole compound used is 5,5′-dithiobis(1,3,5-thiadiazole-2-thiol), and/or in alternative b), the polyol used is a hydrophobic polyether polyol of the formula (VII), and/or in alternative b), the triglyceride having a hydroxy fatty acid component used is castor oil or ricinoleic acid, and/or in alternative b), the hydrophobic phenol derivative used is cardol, cardanol or anacardic acid, and/or in alternative b), the unsaturated fatty alcohol used is hexadecenol or octadecenol.
4 . The process as claimed in claim 1 , wherein
the compounds of the formulae (I) and (II) in alternative a) are used with a proportion by weight of 4% to 13%, preferably 8% to 10%, and the compounds of the formula (III) in alternative a) are used with a proportion by weight of 30% to 95%, preferably 40% to 60%, and the compounds of the formula (IV) in alternative a) are used with a proportion by weight of 10% to 60%, preferably 30% to 50%, or the compounds of the formulae (I) or (II) in alternative b) are used with a proportion by weight of 3% to 6%, preferably 4% to 5%, and the polyols and/or triglycerides with a hydroxy fatty acid component in alternative b) are used with a proportion by weight of 40% to 96%, preferably 50% to 80%, and the hydrophobic phenol derivatives and/or unsaturated fatty alcohols in alternative b) are used with a proportion by weight of 40% to 96%, preferably 50% to 80%.
5 . The lubricant additive obtainable according to claim 1 .
6 . A lubricant additive comprising
I. a dimeric thiadiazole compound, especially a bis(2-alkyl-1,3,4-thiadiazolyl) 5,5′-disulfide derivative of the formula (I)
and/or a dimeric 2,5-dimercapto-1,3,4-thiadiazolethiol derivative of the formula (II)
where n in the formulae (I) and (II) is 1 or 2 and
R1 and R2 are each independently hydrogen, linear or branched alkyl groups having 1 to 12 carbon atoms, especially thioalkyl groups having 1 to 12 carbon atoms, aromatic radicals or heteroaromatic radicals,
II. a polyamine or polyamine derivative of the formula (III)
R1-(CH2-CH2-NH) n -CH2-CH2-R2 (III)
where n in formula (III) is an integer from 1 to 15, especially an integer from 3 to 8, and
R1 and R2 are each independently hydrogen, —NH2, linear or branched alkyl groups having 1 to 12 carbon atoms or a modified or unmodified succinimide group, and
III. a compound of the formula (IV)
in which n is an integer from 1 to 8, especially an integer from 3 to 8, preferably 6.
7 . A lubricant additive comprising
I. a dimeric thiadiazole compound, especially a bis(2-alkyl-1,3,4-thiadiazolyl) 5,5′-disulfide derivative of the formula (I)
and/or a dimeric 2,5-dimercapto-1,3,4-thiadiazolethiol derivative of the formula (II)
where n in the formulae (I) and (II) is 1 or 2 and
R1 and R2 are each independently hydrogen, linear or branched alkyl groups having 1 to 12 carbon atoms, especially thioalkyl groups having 1 to 12 carbon atoms, aromatic radicals or heteroaromatic radicals,
II. a polyol, especially a polyether polyol having a high propylene oxide content, i.e. having a low ethyl oxide/propylene oxide ratio, and/or a triglyceride having a hydroxy fatty acid component, and
III. a hydrophobic phenol derivative and/or unsaturated fatty alcohol.
8 . The lubricant, especially lubricant oil, comprising a lubricant additive as claimed in claim 5 , preferably in a concentration of 0.2% by weight to 10% by weight.
9 . The use of a lubricant additive wherein in claim 5 in lubricants and especially lubricant oils, more preferably in mineral oil-free forming lubricants.Join the waitlist — get patent alerts
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