GB2063909A - High flashpoint hydraulic fluid - Google Patents

High flashpoint hydraulic fluid Download PDF

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Publication number
GB2063909A
GB2063909A GB8033182A GB8033182A GB2063909A GB 2063909 A GB2063909 A GB 2063909A GB 8033182 A GB8033182 A GB 8033182A GB 8033182 A GB8033182 A GB 8033182A GB 2063909 A GB2063909 A GB 2063909A
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Prior art keywords
hydraulic fluid
ester
fluid according
percent
mixture
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GB8033182A
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GB2063909B (en
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ExxonMobil Oil Corp
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Mobil Oil Corp
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    • 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
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
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    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
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    • C10M127/00Lubricating compositions characterised by the additive being a non- macromolecular hydrocarbon
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    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
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    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/08Hydraulic fluids, e.g. brake-fluids

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Lubricants (AREA)
  • Anti-Oxidant Or Stabilizer Compositions (AREA)

Abstract

A hydraulic fluid comprises a blend of 50-97% of an oleic acid ester of a polyol, 3-50% of a mixture of polyols and branched unsaturated C12-20 fatty acids, 0.01-2% of a phenolic antioxidant, 0.01-2% of a diphenyl amine antioxidant, and 1-1000 ppm each of (i) a mixture of a fatty acid partial ester, aliphatic hydrocarbon and silica and (II) a mixture of metal soaps in a hydrocarbon oil, as defoamants.

Description

SPECIFICATION High flashpoint hydraulic fluid This invention relates to hydraulic fluids that are less flammable than fluids based on mineral oils.
The fluids of the present invention are formulated without the use of base fluids which contain phosphorous and chlorine and have, moreover, improved oxidation stability, improved foaming resistance and a low neutralization factor.
Known hydraulic fluids based on esters of polyols with oleic acid or similar materials possess certain disadvantages even though they may be satisfactory in other respects. In particular, the oxidation stability may be unsatisfactory and they may possess high neutralization factors (over 4.0 mg KOH/g). They may also tend to resinify in the presence of air and light.
According to the present invention we provide a hydraulic fluid based on a blend of two basic oil components, a system of two antioxidants having a synergistic effect and a system of two foam inhibitors.
The individual components of the fluid are: (a) an oleic acid ester of a polyol, preferably pentaerythritol-tetraoleate or trimethylolpropanetrioleate, constituting preferably 50 to 97 percent of the blend; (b) a mixture of esters of polyols with branched, predominantly unsaturated C12-C20 fatty acids (neopentyl glycol or trimethylol propane being preferably employed as the polyol component), preferably constituting 3 to 50 percent of the blend; (c) 0.01 to 2.00 percent, preferably 0.20 to 1.00 percent of a phenol derivative having at least one sterically hindered phenol group, i.e. a phenolic hydroxy group immediately adjacent a substituent requiring much space, such as tertiary butyl, (preferably pentaerythrityl-tetrakis [ 3(3,5-di-tertia ry butyl4-hydroxyphenyl)propionate ] , as a phenolic antioxidant;; (d) 0.01 to 2.00 percent, preferably 0.20 to 1.00 percent of a diphenyl amine derivative (preferably a p,p'-dialkyl-diphenyl amine) as an amine antioxidant; (e) 1 to 1000 ppm, preferably 5 to 100 ppm of a mixture of a fatty acid partial ester, an aliphatic hydrocarbon, and finely dispersed silica as a foam inhibitor; and (f) 1 to 1000 ppm, preferably 5 to 100 ppm of a mixture of metal soaps in a hydrocarbon oil as foam inhibitor.
The main component of the product is a polyol-oleic acid ester according to (a). Inclusion of a certain amount of (b) in the formula surprisingly leads to a considerable improvement of the oxidation stability, as is shown in Table I below by comparing Lab. No. 2 and No. 5, without (in spite of the lower viscosity of (b)) affecting the flash point and thus, without noticeably impairing the low inflammability.
In addition, this leads to a more favorable air separating capacity (improvement of 1 to 2 min. at 500C, compared with formulae merely containing (a) as the base oil). Too great proportions of (b) lead to lower flash temperatures and higher inflammability.
Pentaerythrityl-tetrakis [3(3,5-di-tertiarybutyl-4-hydroxyphenyl) propionate] has proved particularly effective as compared with other phenolic antioxidants, as is shown in Table I by comparing Lab. Nos. 1 and 2.
The oxidation stability is further improved with lasting effect by adding (d), as is apparent from Table I by comparing Lab. Nos. 2 and 3 as well as Lab. Nos. 4 and 5.
The synergistic effect of the combination of (c) and (d) is particularly apparent from Table II, as shown by Lab. Nos. 7 and 9 compared with 8.
Although silicone defoamers generally effect sufficient foam inhibition, they also tend to cause a drastic deterioration in the air separating properties. For example, 0.01 percent of a 1 percent solution of dimethyl siloxane polymer in kerosene increases the separation time from 5 to 1 1 min. at 500 C.
Defoamers on the basis of polymeric acrylic acid esters are ineffective in the present ester fluids.
The use of either (e) or (f) by themselves as foam inhibitors results in moderate foam inhibition only, but the combination of (e) and (f) is surprising, and even in very small quantities (10 ppm each) foam formation is effectively inhibited, as can clearly be seen from Table III, while the air separating capacity is not materially impaired.
The hydraulic fluid developed according to the invention has a relatively low neutralization factor (typically about 0.6 mg K0H/g). This contributes to the improved hydrolytic stability of the fluid. In addition, the hydraulic fluid has very favorable toxicological properties and is less aggressive towards seal materials, paint coatings and synthetics than hydraulic fluids based on phosphorus or chlorine compounds.
The hydraulic fluids according to the invention may in addition contain also other agents, such as rust and corrosion inhibitors and metal deactivators.
TABLE I OXIDATION TEST
Pentaaerythrityl tetrakis [3(3,5- 4,4'-Methy- Neutralization di-tert.butylI-4- lene-bis(2,6- p,p'Diocryl Kin. viscosity Factor, Lab. Ester Ester hydroxyphenyl) di-tert. diphenil- Rust Metal (40 C) rise mg.
No. (a) (b) propionate] butylphenol) amine inhibitor Deactivator Rise % KOH/g wt. % 1 98.75 - - 0.50 0.50 0.20 0.05 195 2.0 2 98.75 - 0.50 - 0.50 0.20 0.05 114 1.0 3 99.25 - 0.50 - - 0.20 0.05 506 2.6 4 89.25 10.00 0.50 - - 0.20 0.05 377 2.4 5 88.75 10.00 0.50 - 0.50 0.20 0.05 28 0.4 Test Method: bubble air through sample for 24 hours at 130 C, 10 liters air/hour; oil sample contains steel, copper, aluminum and lead as catalysts.
TABLE Il DIFFERENTIAL THERMAL ANALYSIS 1800C (isotherm), 0.3 1 02/min.
size of sample: 10 mg
pentaerythrityl tetrakis [3(3,5 ester ester di-tert. butyl-4 Lab. accord. accord. hydroxyphenyl) p,p'-dialkyl- I induction No. to (a) to (b) propionate i diphenylamine I period wt. % min.
6 90.00 10.00 - - < 1 7 89.00 1.00 - - 7 8 89.00 10.00 0.50 0.50 14 9 89.00 10.00 - 1.00 1 < 2 Induction period = measured time up to oxidative collapse (strongly exothermic reaction) of fluid.
TABLE Ill FOAM BEHAVIOUR
Foam Test ASTM D Fluid- 892, Sequence I ml Base Fluid (a) 420/130 " + 100 ppm foam 100/5 inhibitor (e) " + 100 ppm foam 190/0 (free after inhibitor (f) 130 s.) 10 10 ppm foam 120/0 (free after inhibitor (e) 90 s.) + 10 ppm foam inhibitor (f)

Claims (7)

1. A hydraulic fluid comprising: (a) 50 to 97 percent of an oleic acid ester of a polyol; (b) 3 to 50 percent of a mixture of esters of polyols and branched, predominantly unsaturated C12-C20 fatty acids; (c) 0.01 to 2.00 percent of a phenolic antioxidant, having at least one sterically hindered phenol group; (d) 0.01 to 2.00 percent of a diphenyl amine antioxidant; (e) 1 to 1000 ppm of a mixture of a fatty acid partial ester, an aliphatic hydrocarbon, and finely dispersed silica; and (f) 1 to 1000 ppm of a mixture of metal soaps in a hydrocarbon oil.
2. A hydraulic fluid according to claim 1 in which the ester (a) is pentaerythritol tetraoleate or trimethylolpropane trioleate.
3. A hydraulic fluid according to claim 1 or 2 in which the ester (b) is an ester of a neopentyl glycol.
4. A hydraulic fluid according to claim 3 in which the neopentyl glycol is trimethylol propane.
5. A hydraulic fluid according to any of claims 1 to 4 in which the antioxidant (c) is pentaerythrityl tetrakis [ 3(3,5-di-tertiarybutyl-4-hydrnxyphenyl)prnpionate ] .
6. A hydraulic fluid according to any of claims 1 to 5 in which the diphenylamine antioxidant is a p,p'-dialky diphenylamine.
7. A hydraulic fluid according to claim 6 in which the diphenylamine antioxidant is p,p'-dioctyl diphenylamine.
GB8033182A 1979-11-29 1980-10-15 High flashpoint hydraulic fluid Expired GB2063909B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE2948020A DE2948020C2 (en) 1979-11-29 1979-11-29 Flame retardant hydraulic fluid

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GB2063909A true GB2063909A (en) 1981-06-10
GB2063909B GB2063909B (en) 1984-02-29

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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0359071A1 (en) * 1988-09-13 1990-03-21 BP Chemicals Limited Fire-resistant hydraulic fluid and process of manufacture
EP0612831A1 (en) * 1992-12-07 1994-08-31 Idemitsu Kosan Company Limited Flame retardant hydraulic oil
US5460741A (en) * 1993-04-09 1995-10-24 Idemitsu Kosan Co., Ltd. Lubricating oil composition
US5607907A (en) * 1993-10-15 1997-03-04 Oronite Japan Limited Multipurpose functional fluid for agricultural machinery or construction machinery
EP0612832B1 (en) * 1992-12-07 1998-07-22 Idemitsu Kosan Company Limited Flame retardant hydraulic oil
US5985806A (en) * 1999-01-19 1999-11-16 Lambent Technologies Inc Telomerized complex ester triglycerides
WO2002083607A2 (en) * 2001-03-29 2002-10-24 Cognis Deutschland Gmbh & Co. Kg Oxidation-stable hydraulic oil
WO2002092732A2 (en) * 2001-05-15 2002-11-21 Matsushita Electric Industrial Co., Ltd. Lubricant composition and analysis method for same
US6750182B1 (en) 1998-10-09 2004-06-15 Exxonmobil Research And Engineering Company Polar oil based industrial oils with enhanced sludge performance

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1249803A (en) * 1969-05-02 1971-10-13 Castrol Ltd Improvements in or relating to hydraulic fluids
GB1354326A (en) * 1970-06-16 1974-06-05 Ici Australia Ltd Hydraulic fluids
CA935146A (en) * 1971-01-18 1973-10-09 A. Csejka David Hydraulic fluids containing esters of alkoxyacetic acid as base stock
DE2302918C2 (en) * 1973-01-22 1982-04-08 Henkel KGaA, 4000 Düsseldorf New ester oils and their use in lubricants and hydraulic fluids
US3956154A (en) * 1974-02-11 1976-05-11 Stauffer Chemical Company Hydraulic fluid system
GB1460665A (en) * 1974-02-11 1977-01-06 Ciba Geigy Ag Transmission device

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0359071A1 (en) * 1988-09-13 1990-03-21 BP Chemicals Limited Fire-resistant hydraulic fluid and process of manufacture
EP0612831A1 (en) * 1992-12-07 1994-08-31 Idemitsu Kosan Company Limited Flame retardant hydraulic oil
EP0612832B1 (en) * 1992-12-07 1998-07-22 Idemitsu Kosan Company Limited Flame retardant hydraulic oil
US6361711B1 (en) * 1992-12-07 2002-03-26 Idemitsu Kosan Co., Ltd. Flame retardant hydraulic oil containing a synthetic ester formed by reaction of a polyol and a mixture of carboxylic acids including oleic acid and isostearic acid
US5460741A (en) * 1993-04-09 1995-10-24 Idemitsu Kosan Co., Ltd. Lubricating oil composition
US5607907A (en) * 1993-10-15 1997-03-04 Oronite Japan Limited Multipurpose functional fluid for agricultural machinery or construction machinery
US6750182B1 (en) 1998-10-09 2004-06-15 Exxonmobil Research And Engineering Company Polar oil based industrial oils with enhanced sludge performance
US5985806A (en) * 1999-01-19 1999-11-16 Lambent Technologies Inc Telomerized complex ester triglycerides
WO2002083607A2 (en) * 2001-03-29 2002-10-24 Cognis Deutschland Gmbh & Co. Kg Oxidation-stable hydraulic oil
WO2002083607A3 (en) * 2001-03-29 2003-01-09 Cognis Deutschland Gmbh Oxidation-stable hydraulic oil
WO2002092732A2 (en) * 2001-05-15 2002-11-21 Matsushita Electric Industrial Co., Ltd. Lubricant composition and analysis method for same
WO2002092732A3 (en) * 2001-05-15 2003-08-28 Matsushita Electric Ind Co Ltd Lubricant composition and analysis method for same

Also Published As

Publication number Publication date
IT8026035A0 (en) 1980-11-17
IT1134313B (en) 1986-08-13
DE2948020C2 (en) 1984-05-03
GB2063909B (en) 1984-02-29
DE2948020A1 (en) 1981-06-04

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