• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    A lubricating oil based on a mineral or synthetic oil is stabilised against oxidative degradation by the addition of a mixture of at least one specific aromatic amine of the formula I or II and at least one sterically hindered amine. The lubricating oil can contain other antioxidants or other additives. It is preferably a motor oil.
    公开号:SU1736343A3
    申请号:SU4614702
    申请日:1989-07-17
    公开日:1992-05-23
    发明作者:Шумахер Рольф；Ивэнс Замуэл；Дубс Паул
    申请人:Циба-Гейги Аг (Фирма)；
    IPC主号:
    专利说明:

    This invention relates to lubricant compositions that are stabilized against oxidative degradation.
    It is well known and generally used to add lubricants based on mineral oils or synthetic oils to improve their performance properties. Of particular importance are additives against oxidative destruction of lubricants, so-called antioxidants. Oxidative destruction of lubricants, so-called antioxidants. The oxidative degradation of lubricants plays a large role primarily in the case of motor oils, since high temperatures dominate the combustion chamber of the engines and, along with oxygen, there are oxides of nitrogen (NOx), which act as oxidation catalysts.
    Amines and alkylated phenothiazines 1 are used as antioxidants for lubricants.
    It is also known to use aromatic amines in combination with other antioxidants, such as, for example, with triaryl phosphites, thiodipropionates or phenolic antioxidants 2.
    Also known is a base oil-based lubricant containing diarylamines substituted with alkyls 3 as antioxidant additives.
    Vi gj o
    TO
    00

    with
    However, the known additives do not provide sufficiently high antioxidant properties.
    The aim of the invention is to increase antioxidant stability.
    The goal is achieved by the fact that a lubricant containing base oil and an aromatic amine (B) contains the compound of the general formula as the latter ...
    L
    - -vr-- -
    - / IIRT
    kg
    rp, eRi-phenyl, C4-Sv-alkylphenyl, naphthyl;
    R2 is phenyl, С4 is Sv-alkylphenyl, or a compound of the general formula where Нз and R4 are independently of each other C4 is Ce-alkyl, and the composition additionally contains a sterically hindered amine (B) total forma% DK5
    Have
    Vifh mi,
    ° u
    where RS is hydrogen or together with Re denotes O,
    Rb-St-Sb-alkylamino, C1 C12-alkoxy,
    Ci - C4-alkoxy-C1 - C4-alkylamino or a residue of general formula flu
    A-Q-
    CH3 CH5
    whereA - CCA (CH2) psoo-, J
    n 2 - 8,
    or-MH (CH2) tMN-,
    t 5.6;
    R is hydrogen, Ci is C4-alkyl, and the content of mixture B and C is 0.25 to 0.75 wt.% Calculated on the base oil with a mass ratio of components B / C of 3 to 19: 1.
    Examples of the aromatic amine are the following compounds: diphenylamine, N-allyl diphenylamine, 4-isopropoxydiphenylamine, 1M-phenyl-1-naphtylamine, M-phenyl-2-naphthylamine, di-4-methoxyphenylamine, (1,3-dimethylbutyl) - phenyl amine, (1,1,3,3-tetramethylbutyl) -phenyl amine, tert-octylated N-phenyl-1-naphthylamine, technical mixtures, obtained by reciprocal
    five
    0
    0
    five
    about
    five
    0
    five
    modifying diphenylamine with diisobutylene (mono-, di- and trialkylated tert-butyl- and tert-octyldiphenylamines), phenothiazine, N-allylphenothiazine, 3,7-di-tert-octyl-phenothiazine, technical mixtures obtained by reacting phenothiamine azine with diisobutylene.
    It is particularly preferable to use 4,4-di-tert-octyldiphenylamine or 3,7-di-tert-octylphenothiazine as a component, a Blend, and a technical mixture obtained by reacting diphenylamine with diisobutylene, in particular a mixture that contains at most 5 wt. .% diphenylamine, 8-15 wt.% 4-tert-butyldiphenylamine, 24-32 wt.% 4-tert-octyldiphenylamine, 4,4-di-tert-butyldiphenylamine and 2,4,4-tri-tert-butyldiphenylamine, 23-34 wt.% 4-tert- € utilizes -to) 1Al1-diphenylamine, 2,2- and 3,3-di-tert-octyldiphenylamine and 2,4-di-tert-butyl-4, - tert-octyldiphenylamine, 21- 34 ma .% 4,4-di-tretchzhtildifenilamina and 2,4-di-tert-Oak til-4 -tert-butildifenilamina.
    The amount of additive (B) and (C) to the base oil (A) is selected depending on the type of base oil and on the desired degree of stabilization. In general, the sum of B and C is 0.25 - 0.75 wt.% Based on A. The ratio of B and Vmozhn vary widely, in general, B in quantitative terms - the predominant component. Preferably the ratio is B / B 3-5: 1.
    As a base oil, mineral or synthetic oil can be used, which is commonly used to prepare lubricants.
    The lubricant may additionally contain additives, such as, for example, other antioxidants, metal passivators, rust inhibitors, substances that improve the viscosity index, decrease the freezing point of the substance, dispersants, surfactants or anti-wear additives.
    Separate additives are dissolved in -L oil. To speed up the dissolving process, the oil is preheated or dissolved prior to the addition in the solvent.
    Example 1. Using a differential scanning calorimeter (DuPont Thermal Analyzer 1090), the induction time of oxidation of oil samples with air, which contains 400 ppm N02, is measured under isometric conditions. The measurement was carried out at 170 ° C under a pressure of 8 bar. Standard mineral oil (Aral 136) is used as the base oil, to which 1% by volume 1-decene is added to increase the sensitivity to oxygen. TO
    The following amine stabilizers are added to the oil.
    Aromatic Amines:
    A-1 is a technical mixture obtained by reacting diphenylamine with diisobutylene, containing 3% by weight of diphenylamine, 14% by weight of 4-tert-butyldiphenylamine, 30% by weight of 4-tert-octyldiphenylamine, 4.4 -di-tert-butyldiphenylamine and 2,4,4-tri-tert-butyldiphenylamine, 29 wt.% 4-tert-butyl-4-tert-octyldiphenylamine, 2,2- and 3,3 -di-tert-octyldiphenylamine and 2,4-di-tert-butyl-4-tert-octyldiphenylamine, 18 wt.% 4,4-di-tert-octyldiphenylamine, 6 May.% 2,4-di-tert-octyl-4-tert-butyl dife - Nylamine;
     - 3,7-di- (tert-octyl) -phenothiazine.
    Spatially hindered amines:
    H-1-di- (2,2,6,6-tetramethylpiperidin-4-yl) -sebacinate;
    H-2 - 2,2,6,6-tetramethyl-4-piperidone;
    H-3 - di- (2,2,6,6-tetramethylpiperidin-4-yl) succinate;
    H-4 - di- (1,2,2,6,6-pentamethylpiperidin-4-yl) sebacinate;
    H-5, 2,3,6-trimethyl-2,6-diethyl-4-piperidone;
    H-6 - 2,2,6,6-tetramethyl-4-butylaminopiperidine.
    Table 1 shows the induction time: the higher the induction time, the higher the antioxidant effect of the stabilizing additive.
    EXAMPLE 2. Oxidation of hydrocarbons produces oxygen-containing groups, such as hydroxyl, carboxyl or ester groups. Using IR spectroscopy, the number of such groups can be well measured and from this measurement the activity of antioxidants can be determined. For this purpose, samples of standard mineral oil (Aral R 136), which is admixed to increase the sensitivity to oxygen by 1 vol.% 1-dexter, are heated under isothermal conditions in an atmosphere of air, which is admixed with 400 ppm N02 under a pressure of 8 bar for 12 hours. Then the IR absorption is measured at 1730 and 1630. The lower these values, the higher the activity of the stabilizers of Tables 2a and 26 show the results at different temperatures.
    KO- -SNgSNgShndak
    TOST method (turbine Oxidation Stabilitg test) according to ASTMD-943. For this purpose, 300 ml of mineral oil (Mobile TOC K 305) is mixed with 60 ml of water and heated in oxygen for 1000 h at 95 ° C in the presence of iron and copper wire. The formation of acids is measured by determining the neutralization number TAN (mg KOH / g oil), as well as the amount of precipitate formed.
    Amine A-1 is used as a stabilizer individually and in a mixture with hindered amine H-7 (2,2,6,6-tetramethyl-4-dodecyloxypiperidine), and
    the concentration of stabilizers is always 0.25% in terms of oil (see tab. 3),
    EXAMPLE 4 Analogously to Example 1, the oxidation induction time was measured at 170 ° C. The following hindered amines are used: H-8 -N, N -bis- (2,2,6,6-tetramethylpiperidin-4-yl) -hexamethylene diamine;
    H-9 is N, -bis (2,2,6,6-tetramethylpiperidin-4-yl) -pentamethylenediamine;
    H-10 - 4- (3-methoxypropylamino) - 2,2,6,6-tetramethylpiperidine (see tab.4).
    EXAMPLE 5 Analogously to Example 1, the oxidation induction time at 170 ° C is measured. It is used as an aromatic amine (A-3) (p-octylphenyl) -1-naphthylamine (see table 5).
    EXAMPLE 6 The oxidation rate can also be measured by measuring the increase in viscosity when treated with oxygen.
    elevated temperature.
    To this end, a stream of oxygen (1 l / h) is passed through the oil for 70 hours at 150 ° C. The oil is pre-sensitized with a catalytic amount
    copper naphthenate. The viscosity of the oil is measured before and after using an Uberlode viscometer (see table 6).
    45
    权利要求:
    Claims (1)
    [1]
    Invention Formula
    A lubricant composition containing a base oil and an aromatic amine, characterized in that, in order to increase antioxidant stability, the composition as an aromatic amine (B) contains a compound of the general formula
     OOSSNgSKg- / 5-OK
    EXAMPLE 3: The oxidation behavior of lubricants stabilized according to the invention is also tested according to
    RR,
    YA |
    where RI is phenyl, C4-Sv-alkylphenyl, naphthyl;
    R2 is phenyl, SL - CA-alkylphenyl, or a compound of the general formula
    where Nz and R4 - independently from each other CA - Sz-alkyl,
    and the composition further comprises a sterically hindered amine (B) of the general formula
    H
    h
    where RS is hydrogen or together with Re denotes O; R - Ci - Cs-alkylamino, Ci - C12-alkoxy, C 1 -C 4 -alkoxy-C 1 -C 4 -alkylamino or a residue of the general formula
    SA
    Kjhtt
    CH3
    where (CH2) psoo-, - 8,
    OR-MH (CH2) tMN-,
    t 5.6;
    R is hydrogen. Ci is C4 alkyl, and the content of the mixture of B and C is 0.25 to 0.75 May. % calculated on the base oil with a mass ratio of B / B equal to 3 - 19: 1,
    L
    Table 1
    Table 2
    Compound of formula
    173634310
    Continuation of table 2
    Table 3
    Table 4
    Table 5
    Table b
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    法律状态:
    2010-09-20| REG| Reference to a code of a succession state|Ref country code: RU Ref legal event code: MM4A Effective date: 20070718 |
    优先权:
    申请号 | 申请日 | 专利标题
    CH273788|1988-07-18|
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