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AU655345B2 - Lubricant for refrigerating machine employing refrigerant comprising tetrafluoroethane - Google Patents
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AU655345B2 - Lubricant for refrigerating machine employing refrigerant comprising tetrafluoroethane - Google Patents

Lubricant for refrigerating machine employing refrigerant comprising tetrafluoroethane Download PDF

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Publication number
AU655345B2
AU655345B2 AU32079/93A AU3207993A AU655345B2 AU 655345 B2 AU655345 B2 AU 655345B2 AU 32079/93 A AU32079/93 A AU 32079/93A AU 3207993 A AU3207993 A AU 3207993A AU 655345 B2 AU655345 B2 AU 655345B2
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AU
Australia
Prior art keywords
carbon atoms
lubricant
group
glycol compound
tetrafluoroethane
Prior art date
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AU32079/93A
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AU3207993A (en
Inventor
Tadashi Katafuchi
Akira Nakamura
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Idemitsu Kosan Co Ltd
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Idemitsu Kosan Co Ltd
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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
    • C10M169/041Mixtures of base-materials and additives the additives being macromolecular compounds only
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    • 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
    • C10M105/02Well-defined hydrocarbons
    • C10M105/06Well-defined hydrocarbons aromatic
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    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/02Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
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    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/20Lubricating compositions characterised by the base-material being a macromolecular compound containing oxygen
    • C10M107/30Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M107/32Condensation polymers of aldehydes or ketones; Polyesters; Polyethers
    • C10M107/34Polyoxyalkylenes
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    • C10M111/04Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a macromolecular organic compound
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    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
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    • C10M171/00Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
    • C10M171/008Lubricant compositions compatible with refrigerants
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    • C10M7/00Solid or semi-solid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single solid or semi-solid substances
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    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
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    • C10M2205/028Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
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  • General Chemical & Material Sciences (AREA)
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  • Lubricants (AREA)

Description

I 1 i i i i I
AUSTRALIA
Patents Act 655345 COMPLETE SPECIFICATION
(ORIGINAL)
Class Int. Class Application Number: Lodged: Complete Specification Lodged: Accepted: Published: 1; Ii 1 Priority Related Art: Name of Applicant: Idemitsu Kosan Co., Ltd.
Actual Inventor(s): Tadashi Katafuchi Akira Nakamura Address for Service: PHILLIPS ORMONDE FITZPATRICK Patent and Trade Mark Attorneys 367 Collins Street Melbourne 3000 AUSTRALIA I' 'Invention Title: LUBRICANT FOR REFRIGERATING MACHINE EMPLOYING REFRIGERANT ':*"COMPRISING TETRAFLUOROETHANE Our Ref 316992 SPOF Code: 93170/47107 4 The following statement is a full description of this invention, including the best method of performing it known to applicant(s): -1- 6006 ir-- LUBRICANT FOR REFRIGERATING MACHINE EMPLOYING REFRIGERANT COMPRISING TETRAFLUOROETHANE i 1 t t it:f I,,ir BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a lubricant for refrigerating machines employing a refrigerant comprising tetrafluoroethane. More particularly, it relates to a lubricant for refrigerating machines which is used along with a refrigerant comprising a substitute fluorohydrocarbon (hereinafter sometimes referred to as "flon compound") such as 1,1,1,2-tetrafluoroethane (R-134a). As such, the lubricant is excellent in the performance such as wear resistance, electrical insulating properties, hydrolytic stability, nonhygroscopicity and the like and further has excellent returnability of the o lubricant in a compression-type refrigerating cycle (the °o characteristics that the lubricant is inclined to return to a so a* 0 compressor after it is circulated in the refrigerating cycle).
2. Description of the Related Arts Conventionally, in a compression-type refrigerating cycle comprising a compressor, a condenser, an expansion valve and an o evaporator, a flon compound including a fluorinated hydrocarbon such as dichlorodifluoromethane (R-12) and chlorodifluoromethane (R-22) has been used as the refrigerant. Many kinds of lubricants compatible with them have also been produced industrially available for use.
However, there have been misgivings that these flon 1f- -f i, compounds widely used as the refrigerant are liable to cause depletion of the ozone layer and environmental pollution after they are released into the open air. In an effort to prevent environmental pollution, fluorohydronarbons (or chlorofluorohydrocarbons), for examp e 1,1,1,2-tetrafluoroethane (R-134a) and the like have been developed as a possible replacement in recent years. Until now there have been introduced into market many so-called substitute flon compounds with minimized danger of environmental pollution and capable of satisfying said required properties, for example 1,1,2,2tetrafluoroethane (R-134) and the like, as well as R-134a.
These new substitute flon refrigerants are different from conventional flon refrigerants in characteristics. Thus, glycol compounds, ester compounds and the like have been proposed as the lubricant for use in combination with them Patent No.
4,755,316. fafcsc ratentrAplicatiou Ld Op No.51@74 l991), and these patents are intended to dissolve substitute flon refrigerants and lubricants completely so as to provide good returnability of the lubricants.
In an attempt to circulate all over a refrigerating cycle a refrigerant and a lubricant in their completely dissolved state as envisaged by these patents, however, said lubricant must be selected from only a very limited number of compounds acceptable to the chemical properties of substitute flon refrigerants such as R-134a. Accordingly, the selected lubricant is forced to sacrifice certain aspects of the important performance required as the lubricant.
0000 00 0 0 0 o 0000 0 ao oo i 0 00 40 ttt
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A
r!"d 2 -I i i l-x-i~ In fact, polyalkylene glycol compounds and ester compounds thereof, both known as compatible with R-134a, have been found to have insufficient wear resistance, along with faulty electrical insulating properties. It has also been found that the polyalkylene glycol compounds are highly hygroscopic and the ester compounds thereof are hydrolytically unstable. Thus the demand for a solution in these problems has been raised in relevant industrial segments.
The present invention has been completed on the basis of a concept quite contrary to ordinary common knowledge as set forth above, in an effort to find a solution in the problems.
As the result, it has been found that all these aspects of the performance can be unified by using a substance excellent in wear resistance, insulation resistance and the like as the S lubricant, compounding therewith a fluidity improver to improve o the fluidity of the lubricant in the presence of a refrigerant 0o0 (R-134a and the like) and thus providing good returnability of 0 the lubricant in a compression-type refrigerating cycle. It has thus been made possible that a lubricant combined even with a new refrigerant has all the required performance including excellent wear resistance, electrical insulating properties, hydrolytic stability and the like and further ensuring i excellent returnability of the lubricant. The present invention has been accomplished based on this finding.
SUMMARY OF THE INVENTION Therefore, an object of the present invention is to provide a lubricant for refrigerating machines employing a refrigerant i.
3 :1 j comprising tetrafluoroethane, which is excellent in the performance such as wear resistance, electrical insulating properties, hydrolytic stability, nonhygroscopicity and the like and further has excellent returnability of the lubricant. The lubricant can be used along with a substitute flon refrigerant in a compression-type refrigerating cycle without a hitch.
Another object of the present invention is to provide a lubricant for refrigerating machines employing a refrigerant comprising tetrafluoroethane, which is especially effective when used in automobile or household air conditioners and refrigerators and the like, having high industrial usefulness.
machines employing a refrigerant comprising 1,1,1,2tetrafluoroethane or 1,1,2,2-tetrafluoroethane which c prises as an essential component a base oil comprising 40 to 95% by S weight of a synthetic oil formed of a poly-a- efin or a S mixture of a poly-a-olefin and an alkylb ene and 5 to by weight of a fluidity improver mprising at least one compound selected from the group nsisting of a polyoxyalkylene glycol compound, a polysilox e compound and a fluoride of polysiloxane compound.
The lubricant of e present invention can be suitably used in various refri eating machines and ordinarily in a compression-e refrigerating cycle comprising a compressor, a condens an expansion valve and an evaporator.
DES ,PTION OF PREFERRED EMBODIMENTS -As- 3gee1 eG io=h .o
.B
.1 4 -4a- The present invention provides a lubricant for refrigerating machines employing a refrigerant including 1,1,1,2-tetrafluoroethane or 1,1,2,2tetrafluoroethane, said lubricant including a base oil including 60 to 90% by weight of a synthetic oil composed of a poly-a-olefin or a mixture of poly-a-olefin and an alkylbenzene and 10 to 40% by weight of a fluidity improver composed of a polyoxyalkylene glycol compound.
The lubricant of the present invention can be suitably used in various refrigerating machines and ordinarily in a compression-type cycle comprising a compressor, a condenser, an expansion valve and an evaporator.
DESCRIPTION OF PREFERRED EMBODIMENTS As set forth above, the lubricant of the present invention o 00 on 0 0 o oo a o o0000oo 0 00 4a 6 0 o 00 6 *O00~ a 0 ooo 0 0 o 00 a G a a a o o o o a o o 9 o r 0 a a o o o "o o *,io (p00 S 0000 i~-U 4 lj -sqL ri~l e, ~j a a*t t 3 0000 o 00 00 0 06 0 0 4 00 a o 0 O I IIl 00o a 0 0000 rI 1 4 4 1 1 00* I! s 'i i t l t comprises the components and as the essential components, and the synthetic oil constituting the component is a poly-a -olefin or a mixture of a poly-a -olefin and an alkylbenzene.
Various poly-a-olefins can be used and ordinarily are each a polymer of a -olefin having 8 to 14 carbon atoms and a kinematic viscosity of 10 to 350cSt at 40°C. Preferred among them is a polymer of 1-dodecene, a polymer of 1-decene or a polymer of 1-octene, each having a kinematic viscosity of 10 to 350cSt at 40°C. A lubricant containing a synthetic oil comprising such a poly-a-olefin has a lower viscosity at low temperatures in the presence of a tetrafluoroethane refrigerant, and thus returnability of the lubricant is all the more improved.
Various alkylbenzenes can be used as well and ordinarily are each an alkylbenzene having a kinematic viscosity of 5 to 500cSt, preferably 10 to 350cSt at 40°C. Meanwhile, either soft or hard alkylbenzene can be used provided that it meets this condition.
The aikylbenzene is not used singly but in the form of a mixture thereof with said poly-a-olefin as the synthetic oil as the component in the present invention. The mixing ratio of the poly-a -olefin to the alkylbenzene may be appropriately selected according to circumstances and is not particularly limited. Preferably the mixture has a poly-aolefin content of 5% or more by weight, more preferably 5 to by weight, most preferably, when using high viscosity poly-a-olefin having a kinematic viscosity of about 50cSt or more at 40 0 C, 5 to 50% by weight of the mixture. When such a mixture of the poly- 5
-I
cJ~ I. a -olefin and alkylbenzene is used as the synthetic oil as the component the mixing stability of the poly-a -olefin and the fluidity improver as the component is improved. This effect is especially remarkable with the use of a polyoxyalkylene glycol compound as the fluidity improver.
On the other hand, the fluidity improver acts to improve the fluidity of a hydrocarbonic compound at low temperatures (those of the evaporator) in the presence of a small amount of substitute flon refrigerant such as R-134a, so as to provide good returnability of the lubricant in the refrigerating cycle.
The kinematic viscosity of the fluidity improver is not particularly limited but is ordinarily 2 to 100cSt, preferably 3 to 50cSt at A typical example thereof is a polyoxyalkylene glycol compound. Various polyoxyalkylene glycol compounds can be used and an appropriate one may be selected from them according to the intended use. Preferred among them is a polyoxyalkylene glycol compound represented by the general formula o a a o o o 0 (1 a a *o a a I a 1 1 44445 4 0 ,,4 a ti
A
0 R 2 3i I wherein R' is a hydrogen atom, an alkyl group having 1 to carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an alkynyl group having 2 to 10 carbon atoms, an aryl group having 6 to 10 carbon atoms, an aralkyl group having 7 to 10 carbon atoms, an acyl group having 2 to 10 carbon atoms or an aliphatic hydrocarbon group having 2 to 6 bonding links; R 2 is 6
~I
.II~
an alkylene group having 2 to 6 carbon atoms; R 3 is a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an alkynyl group having 2 to carbon atoms, an aryl group having 6 to 10 carbon atoms, an aralkyl group having 7 to 10 carbon atoms or an acyl group having 2 to 10 carbon atoms; n is an integer of 1 to 6; and m is a figure satisfying that the average value of mxn is 2 to The alkyl group having 1 to 10 carbon atoms may be straight chain, branched chain or cyclic. Specific examples of the alkyl group include a methyl group, an ethyl group, a n-propyl group, an isopropyl group, various butyl groups, various pentyl groups, various hexyl groups, various heptyl groups, various octyl groups, various nonyl groups, various decyl groups, a cyclopentyl group, a cyclohexyl group, a phenyl group, a tolyl group, a xylyl group, a benzyl group, a phenethyl group and the like.
An alkyl group having more than 10 carbon atoms leads to the degradation of the effect on improving the fluidity of the lubricant. The alkyl group has preferably 1 to 6 carbon atoms.
An alkyl moiety of said acyl group may be straight chain, 'I branched chain or cyclic. Specific examples of the alkyl moiety of the acyl group include a methyl group, an ethyl group, a npropyl group, an isopropyl group, various butyl groups, various pentyl groups, various hexyl groups, various heptyl groups, various octyl groups, various nonyl groups, a cyclopentyl group, a cyclohexyl group and the like. An acyl group having 7 r- p~more than 10 carbon atoms leads to the degradation of the effect on improving the fluidity of the lubricant. The acyl group has preferably 2 to 6 carbon atoms.
Said R' and R 3 may be same or different one another.
Further .Tore, a plurality of R3s in a molecule may be same or different when n is 2 or more.
When R' is an aliphatic hydrocarbon group having 1 to carbon atoms and 2 to 6 bonding links, the aliphatic hydrocarbon group may be either chain or cyclic. Examples of the aliphatic hydrocarbon group having 2 bonding links include an ethylene group, a propylene group, a butylene group, a pentylene group, a hexylene group, a heptylene group, an octylene group, a nonylene group, a decylene group, a cyclopentylene group, a cyclohexylene group, a vinyl group, an allyl group, a butenyl group, an ethynyl group, a propynyl group, and the like. Examples of the aliphatic hydrocarbon group having 3 to 6 bonding links include a residue after a hydroxyl group is removed from a polyhydric alcohol such as trimethylolpropane, glycerin, pentaerythritol, d ipentaerythritol, sorbitol, 1,2,3-trihydroxycyclohexane and 1,3,5-trihydroxycyclohexane.
An aliphatic hydrocarbon group having more than 10 carbon atoms leads to the degradation of the effect on improving the fluidity of the lubricant. The aliphatic hydrocarbon has preferably 2 to 6 carbon atoms.
R
2 of said general formula is an alkylene group having 2 to 6 carbon atoms and examples of the oxyalkylene group as a o 0 i -eo eidi 0 0000C 0" 0 0o e a 4
I
a.:1 i
I~
t0
I
8 L~ -i ~I repeating unit include an oxyethylene group, an oxypropylene group, an oxybutylene group, an oxypentylene group and an oxyhexylene group. A molecule thereof may comprise either same oxyalkylene groups or two or more different kinds of oxyalkylene groups. Preferably a molecule thereof comprises the alkylene groups each having at least 3 carbon atoms, more preferably 50% or more by mole of the alkylene groups each having at least 4 carbon atoms per oxyalkylene unit.
n of said general formula is an integer of 1 to 6 and depends on the number of bonding links of For example, when R' is a hydrogen atom, an alkyl group, an alkenyl group, an alkynyl group, an aryl group or an acyl group, n is 1. When R' is an aliphatic hydrocarbon group having 2, 3, 4, 5 or 6 bonding links, n is 2, 3, 4, 5 or 6, respectively. Further, m °o is a figure satisfying that the average value of mxn is 2 to and when the average value of nxn .is out of said range, the P object of the present invention is not achieved to a full .o 04 extent.
Other than set forth above, examples of the polyoxyalkylene glycol compound for use in the present invention include a j polyoxyalkylene glycol compound containing at least one lR 4 constitutional unit represented by the general formula (II):
I
R
5
-C-R
6
S(II)
R8 -C C-o-
R
7
R
9 9- 1.
i.
i wherein R 4 is a monovalent hydrocarbon group having 1 to carbon atoms and R 5 to R 9 are each a hydrogen atom or a monovalent hydrocarbon group having 1 to 10 carbon atoms.
Various polyoxyalkylene glycol compounds other than enumerated above can be used in the present invention as well, including those having a glycidyl group, those having a carbonyl bond in the molecule, those resulting from the substitution by a fluorine atom and the like.
Of above-mentioned polyoxyalkylene glycol compounds, a polyoxypropylene glycol compound, a polyoxybutylene glycol compound, a polyoxypentylene glycol compound and a polyoxyhexylene glycol compound are preferably used in the present invention because of their improvement in the mixing stability. Most suitable is a fluidity improver containing or more of at least one compound selected from the group consisting of the polyoxybutylene glycol compound, the polyoxypentylene glycol compound and the polyoxyhexylene glycol compound. It is also preferable that a polyoxyalkylene glycol compound should contain the oxybutylene, oxypentylene and oxyhexylene units to foot up to 50 or more among oxyalkylene units forming the compound.
6: o- -e 1f-PHiVi _in t f F Au i'nv nti -=Lag L It is also effective to use a mixture of 2 or more different fluidity improvers.
The synthetic oil and the fluidity improver are 0$ o
O
04 0 V 0 0 00 0 *1 -1 0 r1i.LLIi- UKIVILUNU ANU I/l I'lA'TllLK Patcnt and Trade Mark Alloncys 367 Collins Sircl Melbourne, Australia Pl183/91 i i mixed at a ratio by weight of 40 to 95%, desirably 50 to particularly desirably 60 to 90% of to 5 to 60%, desirably to 50%, particularly desirably 10 to 40%, respectively of When less than 5% by weight of the fluidity improver is used, the fluidity of the lubricant is undesirably not improved and therefore the sufficient returnability of the lubricant is not achieved as well. On the other hand, when more than 60% by weight of the fluidity improver is used, wear resistance and the like are undesirably degraded. This is accompanied by the degradation of the fundamental performance required for refrigerating machine lubricant, including the reduction of insulation resistance, worsening of hydrolytic stability, the increase in hygroscopicity and the like.
,u The lubricant of the present invention comprises as the essential component the base oil comprising the synthetic oil o^ and the fluidity improver as set forth above and as the Sneed arises various additives can be incorporated therein.
Examples of the additive include an anti-wear additive such as '1 phosphoric acid ester and phosphorous acid ester, an antioxidant, a chlorine scavenger, a metal deactivator, a defoaming agent, a detergent-dispersant, a viscosity index improver, a rust preventive, a corrosion inhibitor and the like.
As set forth above, the lubricant for refrigerating machines employing the refrigerant comprising tetrafluoroethane as claimed herein is excellent in the performance such as wear 7
A
1 1 l.-i resistance, electrical insulating properties, hydrolytic stability, nonhygroscopicity and the like and further has excellent returnability of the lubricant. The lubricant of the present invention can be used along with a substitute flon refrigerant in a compression-type refrigerating cycle without a hitch.
The lubricant of the present invention is especially effective when used in automobile or household air conditioners, refrigerators and the like, having high industrial usefulness.
Next, the present invention will be described in greater detail below, with reference to non-limitative examples and comparative examples.
Examples 1 to 6 and Comparative Examples 1 to 3 The synthetic oils and the fluidity improvers were each mixed as shown in Table 1 to prepare the lubricants for use in following tests. The results thereof are given in Table 2.
a 4 -1 2- Table 1 Mixing Composition Synthetic Oil Fluidity Improver Compound Wt% Compound Wt% Example 1 Poly'- a -olefin*1 30 Poly glycol compound A *4 Alkylbenzene* 2 Example 2 Poly- a -olefin* 1 10 Poly glycol compound A *4 Alkylbenzene* 2 Example 3 Poly- a -olefin*l 80 Poly glycol compound B* 5 EsterA 1 Example 4~ Poly- a -olefin*l 50 Poly gly'col compound B* 5 Alkylbenzene 3 30 Ester A 6 Example 5 Poly- a -olefin*l 20 Poly glycol compound A*II Alkylbenzene 2 Example 6 Poly- a -olefin*l 20 Poly glycol compound A* 4 16 Alkylbenzene* 2 60 Poly glycol compound B* 4I Comparative Alkylbenzene 2 80 Ester B*7I Example 1 Comparative Poly- a -olefin*l 30 Ester Example 2 Comparative Poly- a -olefin*l 10 Ester B *7 Example 3 Alkylbenzene* 3 00 0 00 0 0 00 00 0 If 13 Table 2 Performance Fluidity at low temperatures Wear resistance (relative value) Example 1 20 0 Example 2 25 0 Example 3 16 0 Example 4 30 0 Example 5 18 0 Example 6 20 0 Comparative 100 0 Example 1 Comparative 20 x Example 2 Comparative 20 x Example 3 o 0Oc0 00 0 osr 0 0 oa a o o a«aor o o a or o i t0 4 -14- -iL I .0 Table 2 (continued) caoa o 9 o alo oa D ooao o~oo o o a~o~ oc oo oo oo ao a Performance Insulation resistivity Hydrolysis Hygroscopicity Q cm) Example 1 4.8 x 1014 0 0 Example 2 4.5 x 10'" O O Example 3 2.2 x 10'" O O Example 4 3.5 x 10'" O O Example 5 1.5 x 1014 0 0 Example 6 4.7 x 101'" 0 Comparative 3.0 x 101" 0 0 Example 1 Comparative 1.5 x 1013 x A Example 2 Comparative 1.2 x 1013 x A Example 3 All the lubricants used were mixed with 0.5% by weight of an antiwear additive (phosphoric acid ester). The notes in the tables will be supplemented below: A polymer of 1-decene (a kinematic viscosity of 32cSt at Soft alkylbenzene (a kinematic viscosity of 38cSt at Hard alkylbenzene (a kinematic viscosity of 32cSt at Polyoxybutylene glycol dimethylether (a kinematic viscosity of 32cSt at Polyoxypropylene glycol dimethylether (a kinematic viscosity of 28cSt at 40 C).
An ester of C 7 fatty acid and pentaerythritol (a kinematic viscosity of 30cSt at An'ester of C 7 fatty acid and trimethylolpropane (a kinematic viscosity of 14cSt at I'i D 01 D I OQ00 IO I
UOIOO
a D
~OUO
O
~)00
O
O ~U 0I D t O 1 5
I
t 0 oo o o o o or a sc, ail ~ao c ooro
D
oaoo os o o o or or .a or ri or I rite 1 Iiti Iir f crrr c c The lubricants were evaluated by determining each aspect of the performance thereof in accordance with the following test method: Evaluation of the performance Fluidity of the lubricants at low temperatures A lubricant mixed with 10% of R-134a was collected into a pressure glass tube having a diameter of 8mm, then a steel ball of 3/16in. in diameter was introduced therein and the pressure glass tube was sealed.
After the pressure glass tube was retained at the steel ball was caused to fall to determine the time (second) required until the steel ball reached a point 10cm to 5cm above the bottom of the tube. The result thereof is given in terms of relative value.
Wear resistance The wear test was conducted under the following conditions by using a Falex friction testing machine.
R-13 4 a was blown at a rate of 5 liter/hour, and a test piece was subjected to wear for 60 minutes under a load of 3001bs and at 1,000rpm. Meanwhile, the test pieces such as block and pin were made of a standard material in accordance with ASTM D-3233.
Standard of evaluation (wear amount) 0: less than A: 6.0mg or more to 15mg or less x more than Electrical insulating properties
II
1 6x i The electrical insulating properties was evaluated mutatis mutandis according to JIS C-2101 to determine the volume resistivity (room temperature).
Hydrolytic stability 100g of a lubricant, 10g of R-134a, 5ml of water and copper and iron catalysts were placed in a pressure container having a capacity of 300cc. Then, the pressure container was sealed and retained at 100'C for 5 days and thereafter the rate of a rise in the total acid number was determined.
Standard of evaluation 0: less than O.01mgKOH/g A: O.01mgKOH/g or more to 0.1mgKOH/g or less x more than 0.1mgKOH/g Hygroscopicity of a test sample was placed in a 50cc glass container having a diameter of 30mm The glass container was introduced into a thermostat-humidistat and allowed to stand for 5 days at a temperature of 25"C and under a humidity of 85% and thereafter the water content of the test sample was determined.
Standard of evaluation O: less than 0.03% A: 0.03% or more to 0.1% or less x more than 0.1% 1 7

Claims (14)

1. A lubricant for refrigerating machines employing a refrigerant including 1,1,1,2-tetrafluoroethane or 1,1,2,2- tetrafluoroethane said lubricant including a base oil including 60 to 90% by weight of a synthetic oil composed of a poly-a-olefin or a mixture of poly-a-olefin and an alkylbenzene and 10 to 40% by weight of a fluidity improver composed of a polyoxyalkylene glycol compound.
2. The lubricant according to Claim 1, wherein said poly-a-olefin is a polymer of an a-olefin having 8 to 14 carbon atoms and a kinematic viscosity of 10 to 350cSt at 40 0 C.
3. The lubricant according to Claim 2, wherein said polymer of an a-olefin is a polymer of 1-dodecene, 1-decene or 1-octene, each having a kinematic viscosity of 10 to 350cSt at 40 0 C. 0 0 0 0 0 a J-
4. The lubricant according to any one of the preceding claims, wherein said alkylbenzene is selected from a soft alkylbenzene and a hard alkylbenzene, each having a kinematic viscosity of 10 to 350cSt at 40 0 C.
5. The lubricant according to any one of the preceding claims, wherein said mixture of the poly-a-olefin and the alkylbenzene has a poly-a-olefin content of 5 to 90% by weight of the mixture.
6. The lubricant according to any one of the preceding claims, wherein said fluidity improver as the component (B) has a kinematic viscosity of 3 to 50cSt at 40 0 C.
7. The lubricant according to any one of the preceding claims, wherein said polyoxyalkylene glycol compound is represented by the general formula RI-f-OR2-- OR3 (I) m n wherein R is a hydrogen atom, an alkyl group having 1 to carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an alkynyl group having 2 to 10 carbon atoms, an aryl group having 6 to 10 carbon atoms, an aralkyl group having 7 to carbon atoms, an acyl group having 2 to 10 carbon atoms or an o 2 aliphatic hydrocarbon group having 2 to 6 bonding links; R 3 is an alkylene group having 2 to 6 carbon atoms; R is a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an alkynyl group having 2 to 10 carbon atoms, an aryl group having 6 to carbon atoms, an aralkyl group having 7 to 10 carbon atoms or an acyl group having 2 to 10 carbon atoms; n is an integer of 1 to 6; and m is a figure satisfying that the average value of m x n is 2 to
8. The lubricant according to claim 7, wherein said polyoxyalkylene glycol compound contains 50% or more by mole of alkylene groups each having at least 4 carbon atoms per oxyalkylene unit for each molecule.
9. The lubricant according to any one of claims 1 to 6, wherein said polyoxyalkylene glycol compound contains at least one constitutional unit represented by the general formula (II): 39 -19- 9 V., I. t. R4 S(II) I I C C-O- R RI R 7 R 9 os o, o 6 i6 0 I I 'Il 0L 0«« 06 wherein R 4 is a monovalent hydrocarbon group having 1 to carbon atoms; and R 5 to R 9 are each a hydrogen atom or a monovalent hydrocarbon group having 1 to 10 carbon atoms.
The lubricant according to Claim 7, wherein said polyoxyalkylene glycol compound is a polyoxypropylene glycol compound, a polyoxybutylene glycol compound, a polyoxypentylene glycol compound or a polyoxyhexylene glycol compound.
11. The lubricant according to Claim 1, wherein said fluidity improver of component comprises 5 0%Aor more of at least one compound selected from the group consisting of a polyoxybutylene glycol compound, a polyoxypentylene glycol compound and a polyoxyhexylene glycol compound. 2 0 i_ 1 i, '-l -21-
12. The lubricant according to claim 1, wherein said polyoxyalkylene glycol compound contains oxybutylene units, oxypentylene units and oxyhexlyene units to foot up to 50 or more among oxyalkylene units forming the compound.
13. The lubricant according to claim 1 substantially as hereinbefore described with reference to any one of Examples 1 to 6.
14. A method for effecting lubrication in refrigerating machines employing a refrigerant comprising 1,1,1,2-tetrafluoroethane or 1,1,2,2-tetrafluoroethane and a lubricant as defined by any one of claims 1 to 13. A refrigerating system which comprises a compressor, a refrigerant comprising 1,1,1,2-tetrafluoroethane or 1,1,2,2-tetrafluoroethane, and a lubricant as defined by any one of claims 1 to 13. o o SDATED: 30 September, 1994 S PHILLIPS ORMONDE FITZPATRICK 0 Attorneys for: S° IDEMITSU KOSAN CO., LTD krh/32079a.doc 0 0 0 0 11 Aah I ABSTRACT There has been disclosed herein a lubricant for refrigerating machines employing as a refrigerant 1,1,1,2- tetrafluoroethane or 1,1,2,2-tetrafluoroethane, which comprises as an essential.component a base oil comprising 40 to 95% by weight of a synthetic oil formed of a poly-a -olefin or a mixture of a poly-a -olefin and an alkylbenzene and 5 to by weight of a fluidity improver formed of a polyoxyalkylene glycol compound, etc. The lubricant is used along with a refrigerant comprising a substitute flon compound such as 1,1,1,2-tetrafluoroethane (R-134a), and is excellent in the performance such as wear resistance, electrical insulating o properties, hydrolytic stability, nonhygroscopicity, etc. and 0o° 0 also in returnability of the lubricant. Thus, the lubricant is os especially effective when used in automobile or household air conditioners, refrigerators, etc. having high industrial usefulness. 0 0 0 0 0
AU32079/93A 1992-02-18 1993-01-28 Lubricant for refrigerating machine employing refrigerant comprising tetrafluoroethane Ceased AU655345B2 (en)

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US6251300B1 (en) 1994-08-03 2001-06-26 Nippon Mitsubishi Oil Corporation Refrigerator oil compositions and fluid compositions for refrigerator
ES2131240T3 (en) * 1994-08-03 1999-07-16 Nippon Oil Co Ltd COOLING OIL COMPOSITION AND FLUID COMPOSITION FOR REFRIGERATING MACHINES.
US5648018A (en) * 1995-01-12 1997-07-15 Albemarle Corporation Ester/polyolefin refrigeration lubricant
JP4079469B2 (en) * 1996-06-25 2008-04-23 出光興産株式会社 Refrigerator oil composition
KR100496780B1 (en) * 1996-06-25 2005-09-09 이데미쓰 고산 가부시키가이샤 Refrigerator oil composition
TW385332B (en) * 1997-02-27 2000-03-21 Idemitsu Kosan Co Refrigerating oil composition
BR9810749A (en) * 1997-06-17 2000-09-19 Nippon Mitsubishi Oil Corp Composition of refrigeration machine oil and a composition of a fluid for use in a refrigeration machine
US6299792B1 (en) * 1998-01-16 2001-10-09 E. I. Du Pont De Nemours And Company Halogenated hydrocarbon refrigerant compositions containing polymeric oil-return agents
JP4809607B2 (en) * 2005-01-11 2011-11-09 Jx日鉱日石エネルギー株式会社 Assembly oil and method of assembling components of refrigeration and air conditioning equipment
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