[0001] The present invention relates to refrigerator oil compositions, and specifically
to refrigerator oil compositions which have excellent lubricating property and high
hydrolytic stability and are suitable for use in compression refrigerators operated
using a fluoroalkane refrigerant.
[0002] Refrigerator oils composed of a base oil such as a mineral oil, alkyl benzene, polyglycol,
ester or a mixture thereof and optionally added with an extreme pressure additive
have heretofore been used widely in compression refrigerators which employ CFC-11,
CFC-12, CFC-115, HCFC-22 or the like as a chlorine-containing refrigerant.
[0003] Among these refrigerants, CFC types including CFC-11, CFC-12 and CFC-115 are subjected
to control as they are considered to lead to destruction of the ozone layer. There
is also a move toward controlling hydrogen-containing halogenated hydrocarbon refrigerants
such as HCFC-22 because they are considered to cause destruction of the ozone layer
and global warming.
[0004] Fluoroalkane refrigerants, particularly HFC-32, HFC-125, HFC-134a and HFC-152a are
similar in thermodynamic properties to CFC-12 and HCFC-22 so that they are under investigation
or are being used as substitutes for Cl-containing refrigerants.
[0005] A refrigerator lubricating oil is required to satisfy a variety of properties. Of
these, lubricating property is extremely important from the viewpoint of the reliability
of a refrigerator system.
[0006] As lubricating oils for refrigerators cooled using a Cl-containing refrigerant such
as CFC-12 or HCFC-22, there have been known lubricating oils containing, in addition
to a base oil such as a mineral oil, alkylbenzene or a mixture thereof, a phosphate
ester and/or a tertiary phosphite ester (Japanese Patent Laid-Open No. 91502/1979),
trioleyl phosphate (Japanese Patent Laid-Open No. 86506/1976), a tertiary phosphite
ester (Japanese Patent Laid-Open No. 139608/1979), tricresyl phosphate and/or triphenyl
phosphite (Japanese Laid-Open No. 27372/1980), a phosphate ester and a hydrogen phosphite
ester (Japanese Patent Laid-Open No. 92799/1980), an organomolybdenum compound and
an acid phosphate ester (Japanese Patent Laid-Open No. 75995/1984) or a thiophosphate
(Japanese Patent Laid-Open No.293286/1986).
[0007] Chlorine atoms which are contained in a large amount in the system and bonded to
refrigerant molecules act as an extreme pressure additive, as have already been reported
by Honma et al. in the Preprint D.9 (1989) of the 34-th National Meeting of Japan
Society of Lubrication Engineers, when such conventional lubricating oils are employed
in combination with a Cl-containing refrigerant such as CFC-11, CFC-12, CFC-115 or
HCFC-22. Their function as extreme pressure additives are not particularly important.
The addition of a phosphate ester, tertiary phosphite ester, acid phosphate ester
or hydrogen phosphite ester alone has heretofore been sufficient. However, two or
three extreme pressure additives have ordinarily been used in combination for convenience.
[0008] Fluoroalkane refrigerants containing no chlorine atom or atoms in their molecules,
such as HFC-32, HFC-125, HFC-134a and HFC-152a, however, have no effects as an extreme
pressure additive by themselves so that the addition of an extreme pressure additive
is indispensable for a lubricating oil employed in a compression refrigerators using
a fluoroalkane as a refrigerant.
[0009] It is, on the other hand, important for a refrigerator oil to have good miscibility
with a refrigerant. Refrigerator oils for a fluoroalkane refrigerant employ a base
oil having strong polarity such as an ester oil, carbonate ester oil or polyglycol
oil in view of their miscibility with the refrigerant. Particularly for a hermetic-type
compressor which requires a lubricating oil having high electrical insulating property,
a base oil having strong polarity, such as an ester oil or carbonate oil is employed.
In this case, however, strong polarity of the ester oil significantly deteriorates
physical and chemical adsorption of an extreme pressure additive on a sliding metal
surface, thereby lowering the effects of the extreme pressure additive so added.
[0010] In addition, an ester oil tends to have a large water-in-oil content because of its
high polarity and hygroscopicity. When a hydrolyzable phosphate-ester type extreme
pressure additive is added in a large amount to the ester oil, ferrous and/or ferric
phosphates are formed as a result of a reaction between phosphoric acid, formed by
the hydrolysis of the extreme pressure agent, and iron present in the refrigerator
system. The ferrous and/or ferric phosphates so formed may cause troubles on the refrigerator,
because they become sludge and may clog an expansion valve and/or capillary tubing.
[0011] As disclosed in Japanese Patent Laid-Open Nos. 91502/1979, 86506/1976, 139608/1979
and 92799/1980 and USP 4,755,316, use of a normal phosphate ester such as tricresyl
phosphate or a tertiary phosphite ester as an extreme pressure additive in combination
with a fluoroalkane refrigerant requires addition of a relatively large amount of
the extreme pressure additive to a base oil because, otherwise, no sufficient extreme
pressure effects can be obtained. This, however, leads to formation of sludge in a
large amount, tending to cause the trouble referred to above.
[0012] Further, as disclosed in Japanese Patent Laid-Open No. 102296/1990, dioleyl hydrogenphosphite,
a secondary phosphite ester, may be added to polyoxyalkylene glycol oil in some instances.
Polyoxyalkylene glycol oil having low electrical insulating property is, however,
not suited for hermetic-type compressors employed in refrigerators or the like. There
is hence a demand for the development of a refrigerator oil composition having good
electrical insulating property.
[0013] The present inventors have proceeded with an extensive investigation on lubricating
property and stability when a fluoroalkane is used as a refrigerant and an ester oil
or the like is used as a refrigerator oil. As a result, it has been found that an
abrasion-resistant and practically-usable refrigerator oil composition can be obtained
by using as an extreme pressure additive a secondary phosphite ester, leading to the
completion of the present invention.
[0014] An object of the present invention is to overcome the drawback of a refrigerator
oil composed of an ester oil, neo-acid ester oil or carbonate ester oil, namely, its
poor lubricating property and to provide a refrigerator oil composition which has
excellent abrasion resistance and high hydrolytic stability and is useful in a refrigerant-compression
type refrigerator employing a fluoroalkane as a refrigerant.
[0015] The present invention therefore provides a refrigerator oil composition containing
a base oil and suited for use in a compression-type refrigerator employing a fluoroalkane
as a refrigerant, said base oil comprising at least a synthetic ester oil, which comprises,
based on the total weight of the composition:
0.001-1.0 wt.% of a secondary phosphite ester represented by the following formula
(1):

wherein R¹ and R² may be the same or different and individually represent a C₁₋₂₀
hydrocarbon or oxygen-containing hydrocarbon group.
[0016] The base oil contained in the refrigerator oil composition according to the present
invention is a synthetic ester oil itself or contains a synthetic ester oil as a component.
Any synthetic ester oil is usable as long as it can be employed as a base oil in a
compressor of a refrigerator. Specific examples of the synthetic ester oil include
dibasic acid esters, polyol esters, complex esters and polyol carbonate esters.
[0017] Exemplary dibasic acid esters include esters of C₅₋₁₀ dibasic acids, such as glutaric
acid, adipic acid, pimelic acid, suberic acid, azelaic acid and sebacic acid, and
linear- or branched-alkyl-containing C₁₋₁₅ monohydric alcohols such as methanol, ethanol,
propanol, butanol, pentanol, hexanol, heptanol, octanol, nonanol, decanol, undecanol,
dodecanol, tridecanol, tetradecanol and pentadecanol. Specific examples include ditridecyl
glutarate, di-2-ethylhexyl adipate, diisodecyl adipate, ditridecyl adipate and di-3-ethylhexyl
sebacate.
[0018] As polyol esters, esters of diols or polyols containing 3-20 OH groups and C₆₋₂₀
fatty acids can be used preferably. Preferred diols are C₂₋₁₂ diols. Specific examples
of C₂₋₁₂ diols include ethylene glycol, 1,3-propanediol, propylene glycol, 1,4-butanediol,
1,2-butanediol, 2-methyl-1,3-propanediol, 1,5-pentanediol, neopentyl glycol, 1,6-hexanediol,
2-ethyl-2-methyl-1,3-propanediol, 1,7-heptanediol, 2-methyl-2-propyl-1,3-propanediol,
2,2-diethyl-1,3-propanediol, 1,8-octanediol, 1,9-nonanediol, 1,10-decanediol, 1,11-undecanediol
and 1,12-dodecanediol. As polyols, on the other hand, C₃₋₆₀ polyols are preferred.
Specific examples include polyhydric alcohols such as trimethylolethane, trimethylolpropane,
trimethylolbutane, di(trimethylolpropane), tri-(trimethylolpropane), pentaerythritol,
di-(pentaerythritol), tri-(pentaerythritol), glycerin, polyglycerins (dimer to eicosamer
of glycerin), 1,3,5-pentanetriol, sorbitol, sorbitane, sorbitol-glycerin condensates,
adonitol, arabitol, xylitol and mannitol; saccharides such as xylose, arabinose, ribose,
rhamnose, glucose, fructose, galactose, mannose, sorbose, cellobiose, maltose, isomaltose,
trehalose, sucrose, raffinose, gentianose and melezitose; partially-etherified products
thereof; and methyl glycoside (glycoside).
[0019] Illustrative fatty acids include linear or branched fatty acids such as hexanoic
acid, heptanoic acid, octanoic acid, nonanoic acid, decanoic acid, undecanoic acid,
dodecanoic acid, tridecanoic acid, tetradecanoic acid, pentadecanoic acid, hexadecanoic
acid, heptadecanoic acid, octadecanoic acid, nonadecanoic acid, eicosanoic acid and
oleic acid; and so-called neo-acids having a quaternary α-carbon atom. These polyol
esters may contain one or more free hydroxyl groups. Particularly preferred examples
of polyol esters include esters of hindered alcohols such as neopentyl glycol, trimethylolethane,
trimethylolpropane, trimethylolbutane, di-(trimethylolpropane), tri-(trimethylolpropane),
pentaerythritol, di-(pentaerythritol) or tri-(pentaerythritol). Specific examples
include trimethylolpropane caprylate, trimethylolpropane pelargonate, pentaerythritol
2-ethylhexanoate and pentaerythritol pelargonate.
[0020] The term "complex ester" as used herein means a mixture of esters of a monohydric
alcohol and polyol with a fatty acid and a dibasic acid. No particular limitation
is imposed on their mixing ratio. As the fatty acid, dibasic acid, monohydric alcohol
and polyol, those exemplified above with respect to the dibasic acid ester and polyol
ester can be used.
[0021] The polyol carbonate ester is an ester of a carbonic acid and a polyol. As illustrative
polyols, those exemplified above with respect to the polyol ester, polyglycols obtained
by homo- or co-polymerization of diols as well as those obtained by adding a polyglycol
to the polyols exemplified above can be used.
[0022] The synthetic ester oils described above can be used either singly or in combination.
The kinematic viscosity of the synthetic ester oil in the present invention is 2-150
cSt, preferably 4-100 cSt, at 100°C.
[0023] In the composition according to the present invention, the above synthetic ester
oils, i.e., the oxygen-containing compounds can be used singly. Alternatively, a mineral
oil, a synthetic oil or the like, which is employed in refrigerator oils for chlorine-containing
refrigerants such as CFC-12 and HCFC-22, can also be used in combination. As mineral
oils, paraffin mineral oils, naphthene mineral oils and the like can be used. They
are obtained by subjecting a lubricating oil fraction, which has been obtained by
atmospheric distillation and vacuum distillation of a crude oil, to a suitable combination
of refining treatment steps such as solvent deasphalting, solvent extraction, hydrogenolysis,
solvent dewaxing, catalytic dewaxing, hydrorefining, sulfuric acid treatment and clay
treatment. As synthetic oils, known poly-α-olefins such as polybutene, 1-octene oligomer
and 1-decene oligomer; alkylbenzenes, alkylnaphthalenes, polyglycols and mixtures
of at least two of them are usable. In this case, it is desirable that the synthetic
ester oil is contained in an amount of at least 50 wt.%, preferably at least 70 wt.%,
based on the total amount of the base oil. The preferred dynamic viscosity of the
base oil ranges from 2.0 cSt to 100 cSt at 100°C.
[0024] The composition according to the present invention comprises the base oil described
above and, based on the total amount of the composition, 0.001-1.0 wt.%, preferably
0.005-0.5 wt.% of a secondary phosphite ester represented by the following formula
(1):

wherein R¹ and R² may be the same or different and individually represent a C₁₋₂₀
hydrocarbon or oxygen-containing hydrocarbon group.
[0025] If the content of the secondary phosphite ester is smaller than the above range,
the resultant lubricating oil will be less effective for the improvement of abrasion
resistance. Even if the content exceeds the above range, on the other hand, the resultant
lubricating oil will not show improving effects in proportion to the increase in the
content. Furthermore, the secondary phosphite ester reacts with water existing in
a dissolved form in the synthetic ester oil, thereby forming phosphoric acid. It is
then converted to ferrous and/or ferric phosphates, thereby forming sludge. The sludge
in turn causes clogging of capillary tubing or the like of the refrigerator. Contents
outside the above range, therefore, are not preferred.
[0026] R¹ and R² in the formula (1) may be the same or different and individually represent
a C₁₋₂₀, preferably C₃₋₁₈ hydrocarbon or oxygen-containing hydrocarbon group. Preferred
examples of the hydrocarbon group include alkyl, phenyl, cresyl and xylyl. The term
"oxygen-containing hydrocarbon group" as used herein means a hydrocarbon group in
which at least one of the carbon atoms has been substituted by a corresponding number
of oxygen atom(s). Preferred is the group represented by the formula -(AO)
n-R³ wherein A represents a C₂₋₄ alkylene group, R³ represents a C₁₋₁₈ hydrocarbon
group (preferably, an alkyl group) and n represents an integer of 1-20. Specific examples
of the C₁₋₂₀ alkyl group include methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl,
sec-butyl, tert-butyl, n-pentyl, iso-pentyl, neo-pentyl, n-hexyl, iso-hexyl, n-heptyl,
iso-heptyl, n-octyl, iso-octyl, n-nonyl, isononyl, n-decyl, iso-decyl, n-undecyl,
iso-undecyl, n-dodecyl, iso-dodecyl, n-tridecyl, iso-tridecyl, n-tetradecyl, iso-tetradecyl,
n-pentadecyl, iso-pentadecyl, n-hexadecyl, iso-hexadecyl, n-heptadecyl, isoheptadecyl,
n-octadecyl, iso-octadecyl, n-nonadecyl, iso-nonadecyl, n-eicosyl and iso-eicosyl
groups.
[0027] To improve the overall performance of the refrigerator oil composition of the present
invention, the composition can be added with one or more of ordinarily-used additives,
for example, scavengers for acid substances and/or active substances such as free
radicals, e.g., phenyl glycidyl ether, butylphenylglycidyl ether, nonylphenyl glycidyl
ether, polyalkyleneglycol glycidyl ether and epoxy compounds such as epoxylated vegetable
oils; phenol-type and amine-type antioxidants; oiliness improvers such as higher
alcohols and higher fatty acids; metal deactivators such as benzotriazole. These additives
can be added in proportions generally employed.
[0028] Specific examples of the refrigerant usable in combination with the refrigerator
oil composition of the present invention include fluoroalkane refrigerants such as
difluoromethane (HFC-32), trifluoromethane (HFC-23), pentafluoroethane (HFC-125),
1,1,2,2-tetrafluoroethane (HFC-134), 1,1,1,2-tetrafluoroethane (HFC-134a) and 1,1-difluoroethane
(HFC-152a).
[0029] The refrigerator oil compositions according to the invention can be widely used in
apparatuses employing a hermetic refrigerant-compression type refrigerator, such as
refrigerators, freezing chambers, automatic vending machines, display cases, room
air conditioners and dehumidifiers and also in refrigerators of other types.
[0030] When a refrigerator oil composition according to the present invention is used in
such a refrigerant-compression type refrigerator as exemplified above, it is ordinarily
used in the form of a fluid composition containing the above refrigerant mixed therein.
No particular limitation is imposed on their mixing ratio, however, it is desirable
to use, in a mixed state, 1-500 parts by weight, preferably 2-400 parts by weight
of the refrigerator oil composition per 100 parts by weight of the refrigerant.
[0031] A refrigerator oil composition according to the present invention has excellent abrasion
resistance and tends to form less sludge so that it can be used as a preferred refrigerator
oil for a fluoroalkane refrigerant containing as a base oil a synthetic ester oil.
[0032] The present invention will next be described in detail by the following examples
and comparative examples. It should however be borne in mind that this invention is
by no means limited to or by the examples. Examples 1-9.
[0033] In order to evaluate the performance of refrigerator oil compositions of the present
invention, their lubricating property was evaluated using a high-pressure atmosphere
friction tester which was reported under B-S7 at the Tribology Conference held by
Japan Society of Lubrication Engineers in the spring of 1991 in Tokyo. Hydrolytic
stability was also evaluated at the same time. The results are shown in Table 1.
[0034] For comparison, evaluation results of comparative products with which one or more
extreme pressure additives had been blended in a conventional manner are also presented
in Table 1.
[0035] Incidentally, the base oils employed in the Examples and Comparative Examples and
their properties are shown in Table 2.
[Wear Test]
[0036] A sample refrigerator oil composition (420 g) and 150 g of 1,1,1,2-tetrafluoroethane
(HFC-134a) were weighed in a high-pressure metal vessel. In a state dipped in the
resulting mixture which had been heated to 80°C, a disc-shaped stationary test piece
(made of SCM3 cast iron) was placed on a loading arbor installed on an inner bottom
of the vessel. Three vanes (made of S-55C cast iron) of 1 mm wide were brought into
contact with the test piece, whereby a wear test was conducted for 6 hours at 500
rpm under a load of 250 kgf. After the completion of the test, a wear loss of the
disc-shaped test piece was determined in terms of weight.
[Hydrolysis Test]
[0037] A sample refrigerator oil composition (100 g) was weighed in a 200-mℓ glass test
tube. Three iron sheets having a surface area of about 10 cm² were placed in the test
tube as a deterioration accelerating catalyst. The test tube was placed in a stainless-steel
autoclave and dissolved oxygen in the refrigerator oil composition was purged out
in a vacuum. Purified water (0.1 g) was then added to the refrigerator oil composition.
After the autoclave was hermetically sealed, the resulting mixture was heated at 150°C
for 2 weeks. The sample oil thus treated was filtered through a membrane filter having
a pore size of 0.4 µm. The filtrate was washed with hexane. The weight of a precipitate
so collected was recorded as the weight (mg) of sludge formed per 100 g of the sample
refrigerator oil composition.
[0038] As can be seen from Examples 1-9 in Table 1, even though the amount of the secondary
phosphite ester added to the polyol tetraester, that is, a base oil, was small, the
resulting refrigerator oil composition according to this invention showed excellent
wear resistance in the refrigerant, namely, 1,1,1,2-tetrafluoroethane or difluoromethane
compared with the composition in Comparative Example 2 which contained tricresyl phosphate,
a conventional extreme pressure additive. Further, the former composition produced
by far less sludge than the latter and thus, was superior in hydrolytic stability.