• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
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    • 专利摘要:
    1462027 Mixed esters SNAMPROGETTI SpA 21 April 1975 [8 May 1974] 16480/75 Heading C2C [Also in Division C5] Mixed esters prepared by reacting (a) a mixture of (i) at least one polyol containing 3 hydroxy groups, (ii) at least one polylol containing 4 hydroxy groups and optionally (iii) at least one polyol containing more than 4 hydroxy groups in a molar ratio of (i) to (ii) and (iii) in the range 0À5 1 to 10 : 1 and wherein ratio of (iii) to (ii) is in the range 0 : 1 to 1À2 : 1 with (b) a mixture of (i) at least one saturated linear monocarboxylic acid (7-8 C) and (ii) at least one saturated linear monocarboxylic acid (12-18 C) wherein the molar ratio of acid(s) (i) to acid(s) (ii) is in the range 1À5 : 1 to 6 : 1 are used as lubricants alone or admixed with mineral oil. The reaction may be in the presence of a solvent at 70‹ to 260‹ C. with or without conventional catalysts. Examples describe the reaction of dodecanoic and heptanoic acids with 1,1,1-tri-(hydroxymethyl) propane and pentaerythritol; dodecanoic, heptanoic and hexadecanoic acids with THMP, pentaerythritol and dipentaerythritol; heptanoic, dodecanoic and hexadecanoic acids with THMP, pentaerythritol and dipentaerythritol; hexadecanoic, dodecanoio, octanoic and heptanoic acids and THMP, pentaerythritol and dipentaerythritol; and heptanoic, octanoic and dodecanoic acids with THMP, pentaerythritol and dipentaerythritol.
    公开号:SU743579A3
    申请号:SU752129353
    申请日:1975-05-07
    公开日:1980-06-25
    发明作者:Манчини Джузеппе；Импарато Луиджи；Скиллани Дарио
    申请人:Снапрогетти С.П.А. (Фирма)；
    IPC主号:
    专利说明:

    I
    This invention relates to a process for the preparation of a new lubricating oil based on a mixture of esters of the general formula
    CH OCOTl SIz-CH-C-O120COR
    sngoson
    scoax xyoskg-s-schoon and
    CHjOCOR
    sigosok
    RCOOCHj-C-CH20Cll2- (s-CH20COft
    CHgOCOKCHjOCOK
    where R- - (СН), n - 5-6 and 10-16.
    It is known to use esters as lubricating oils, which are obtained by the reaction of pentaerythritol (PeE) or dipentaerythritol (DpeE) or trimethylolpropane (TMP) with monocarboxylic acids.
    TMP with nonanoic and isodecanoic acids 1 gives ether with viscosity at 98.9 ° С equal to 6.25 eats, viscosity index (IV) 106, with pentanoic acid
    2-ethylhexanoic, tetradecanoic acids get a product with a viscosity at 98.9 ° С equal to 5.83 eats, and. at. 131, pour point -.
    Similarly, PeE with isooctane and nonanoic acids gives a viscosity at 98 equal to 6.81 eats, iv. 115; Pour point - 4.0С,
    to a mixture with heptanoic and nonanoic acids gives a viscosity at 98.9 ° C equal to 5.23 eats, iv 125, a pour point of -20 ° C, a mixture of octane, nonanoic and decanoic acid gives a viscosity at 98.9 ° C equal to 6.42 eats, iv. 143; pour point + 4 ° С.
    Derivatives of DPEE are also not input a
    20 in the specified viscosity range also due to the use of acids having a short chain, for example, hexabutanate has a viscosity at 98, above 8 eats.
    The purpose of the invention is a method for obtaining a new lubricating oil with a minimum pour point and the highest possible viscosity index.
    This is achieved by the proposed
    30 method of producing lubricating oil
    based on a mixture of esters of the formula
    CHgOCOR
    cKj-cng-e-CHzqcoB
    CWgOCOK
    RCOOCHj-C-CH OCOH and
    knock
    SNGOSON with Zosk 1: coaxi-1: -cH20CH2-c-CH20cOR
    CH20SOT1 snowboard
    where R- - (CH2) pSN. , p - 5-6 and 10-16,
    interaction between a mixture of trimethylolpropane, pentaerythritol, and dipentaerythritol, in which the molar ratio of trimethylolpropane: the sum of pentaerythritol and dipentaerythritol is 0.5: 10, and the ratio of dipentaerythritol: pentaerythritol is 0: 1.2, with a mixture of carboxylic acids and an acid – iz, i have an iztool. acids with 7-8 carbon atoms to acids with 12-18 carbon atoms is 1.5: 6 at a temperature of 210-240 ° C.
    The reaction between acids and polyols occurs in a single phase and is carried out predominantly in the presence and at a temperature of from 70 to, more preferably from 150 to 250 s.
    Water is removed by purging with nitrogen or another inert gas or by conducting the reaction under moderate vacuum.
    The post-reaction treatment is sustained by washing with an aqueous solution of alkali (and then water) if a non-volatile catalyst is used and then in a priming gas with an inert gas or using reduced pressure to remove traces of water and by-products having a lower boiling point.
    If the catalyst is not used, alkaline washing can be avoided and the product can be directly purged and, if possible, residual acids can be removed by one of the methods used and known for this, for example, by treatment with a solid adsorber separated by filtration, etc.
    Example 1. Product A.
    In a glass flask equipped with a stirrer, a nitrogen inlet pipe with a thermometer and a water separator with the appropriate cooler, nitrogen is passed through the interaction with 1.147 mol (229.4 g) of dodecanoic acid, mol (254.26 g) of heptanoic acid, 0.9 (120, 76 g) trimethylolpropane (TiP) and 0.1 mol (13.61 g) of pentaerythritol ().
    The temperature is gradually increased so that after 2.5 hours it reaches 210 ° C and the next 4 hours it is maintained at 215-220 C and finally raised to 230-240 0 and maintained for 12 hours. The separator collects most of the reaction water. An excess of the initial mixture of acids, corresponding to 10% of the initially loaded amount, is added, then the reaction is continued for another 4 hours at 230 ° C.
    Then purge with nitrogen at 230 ° C. After 3 hours, the acidity was 0.3 mg KOH / g and the viscosity 5 eats at. Purging is continued for another hour until the acidity of 0.05 mg KOH / H is reached. Yield 94%.
    Example 2. Product B.
    Under the conditions of Example 1, 0.34 mol (45.6 g) TIP, 0.075 mol (10.2 g) PeE, 0.005 mol (21.6 g) DPeE, 1.464 mol (190.6 g) heptanoic acid are reacted, 0.22 L (44.1 g) of dodecanoic acid and 0.146 mol (37.44 g) of hexadecanoic acid.
    To complete the reaction, 6-8 g of the initial mixture of acids is added.
    After purging with nitrogen and subsequent filtration, the acidity is 2 mg KOH / H. Then, after treatment with alumina, the acidity is 0.65 Mg KOH / G and the viscosity of the final product 6.21 eats at 99 ° C.
    Example 3. Product C.
    Under the conditions of Example 1, 0.15 mol (20.13 g) TIffl, 0.2 mol (27.23 g) PeE, 0.075 mol (19.05 g) DPeE, 0.051 mol (13.08 g) hexadecane are reacted acid), 0.204 mol (98.07 g) dodecanoic acid and 0.765 mol of heptanoic acid. After purging with nitrogen, the acidity is 0.1 mg KOH / g and the viscosity at 6.61 units.
    Example 4. Product D.
    Analogously to example 1, take 0.13 mol (33.02 g) of DPeE, 0.20 mol (27.23 g) of PeE, 0.17 mol (22.81 g) of TYPE, 1.105 mol of (143.86 g) of heptanoic acid , 0.65 mol (93.74 g) octanoic acid and 0.334 mol (66.9 g) dodecanoic acid.
    After purging with nitrogen and final filtration, the acidity is 0.04 mg KOH / g. Viscosity at equal to 6.65 eats.
    Example 5. Product E.
    Analogously to example 1, take 0.32 mol (42.9 g) TIP, 0.10 mol (13.6 g) PeE, 0.0.8 mol (20.3 g) DPE, 0.368 mol (73.7 g) dodecanoic acid , 0.920 mol (119.8 g) of heptanoic acid and 0.552 mol (79.6 g) of octanoic acid.
    The finished product has a viscosity at 5.85 set and an acidity of 0.84 mg KOH / g.
    Table 1 shows the characteristics of the products.
    Table 2 shows the rheological properties of the products.
    Table 1
    权利要求:
    Claims (1)
    [1]
    Claim
    A method of obtaining a lubricating oil based on a mixture of esters of the General formula ch 2 ocor
    I
    CHj — sn 2 - C — CH 2 OS OR ch 2 ocor CH 2 OCOR45
    RCOOCH3 — C — CH 2 OC0R and ch 2 ocor ch 2 ocor ch 2 ocor50
    RCOOCH Z -c — ck 2 res 2 - c - CB 2 OC0NO 2 axes ch 2 ocor where R— - (CHg) n CHy η - 5-6 th 10-16, characterized in that the mixture is trimethylolpropane, pentaerythritol and dipentaerythritol in which the molar ratio of trimethylolpropane: the sum of pentaerythritol and dipentaerythritol is 0.5: 10, and the ratio of dipentaerythritol: pentaerythritol is 0: 1.2, is reacted with a mixture of carboxylic acids in which the molar ratio of acids with 7-8 carbon atoms to acids with 12-18 carbohydrate atoms is equal to 1.5: 6 at a temperature of 210-240 ° C in the last stage of the reaction.
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    同族专利:
    公开号 | 公开日
    DD119204A5|1976-04-12|
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    NL181105B|1987-01-16|
    ZA752955B|1976-03-31|
    DE2520459C3|1989-05-18|
    CS187321B2|1979-01-31|
    DK147978C|1985-08-26|
    DD124389A5|1977-02-16|
    DE2520459B2|1979-06-21|
    NO143529C|1981-03-04|
    AU8010075A|1976-10-21|
    FR2270230B1|1977-12-09|
    BE828807A|1975-09-01|
    YU104775A|1981-04-30|
    JPS5726554B2|1982-06-04|
    LU72396A1|1975-08-26|
    IT1010487B|1977-01-10|
    PL102226B1|1979-03-31|
    SE426389B|1983-01-17|
    NO751627L|1975-11-11|
    HU170743B|1977-08-28|
    DK147978B|1985-01-21|
    CA1060040A|1979-08-07|
    RO70591A|1980-08-15|
    NO143529B|1980-11-24|
    NL7505342A|1975-11-11|
    SE7505291L|1975-11-09|
    YU36191B|1982-02-25|
    DK203475A|1975-11-09|
    JPS50153172A|1975-12-09|
    GB1462027A|1977-01-19|
    CH617419A5|1980-05-30|
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    US4025447A|1977-05-24|
    引用文献:
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    US3309318A|1965-04-30|1967-03-14|Emery Industries Inc|Blends of ester lubricants|
    US3673226A|1968-04-10|1972-06-27|Ethyl Corp|Synthetic lubricants|
    GB1301003A|1969-07-10|1972-12-29|Ethyl Corp|Lubricant materials|
    US3670013A|1969-10-16|1972-06-13|Hercules Inc|Synthesis of partial esters of certain poly and aliphatic monocarboxylic acids|US4144183A|1973-01-22|1979-03-13|Henkel Kommanditgesellschaft Auf Aktien|Mixed branched and straight chain ester oils|
    IT1050335B|1975-12-11|1981-03-10|Snam Progetti|ORGANIC ESTERS TO BE USED IN LUBRICANT COMPOSITIONS|
    US4290337A|1977-01-03|1981-09-22|Nittetsu Bolten Kabushiki Kaisha|Fastener set|
    US4477383A|1982-05-05|1984-10-16|National Distillers And Chemical Corporation|Di- and tripentaerythritol esters of isostearic acid|
    JPH0119689Y2|1982-10-22|1989-06-07|
    JPS5965101U|1982-10-25|1984-05-01|
    JPS5965103U|1982-10-26|1984-05-01|
    JPH0730345B2|1986-09-08|1995-04-05|出光興産株式会社|Lubricating oil composition|
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    US20040075079A1|1998-10-13|2004-04-22|Unichema Chemie Bv|Hydraulic fluids|
    CN1084786C†|1996-04-16|2002-05-15|尤尼剑马化学股份有限公司|Fluides hydrauliques|
    US20110118432A1|2008-07-18|2011-05-19|Huntsman Petrochemical Llc|Natural oil based autocatalytic polyols|
    ES2751551T3|2015-06-12|2020-04-01|Novamont Spa|Low pour point trimethylolpropane esters|
    JPWO2019087351A1|2017-11-02|2020-09-24|花王株式会社|Lubricating oil base oil and a lubricating oil composition containing the lubricating oil base oil|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    IT22398/74A|IT1010487B|1974-05-08|1974-05-08|ESTERS AS COMPONENTS OF LUBRIFI CANTI|
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