Technical Field
[0001] The present invention relates to a working fluid composition for a refrigerating
machine, and more specifically relates to a working fluid composition for a refrigerating
machine that contains a mixed refrigerant which contains a hydrofluoroethane, difluoromethane
(also referred to as "HFC-32" or "R32") and tetrafluoropropene.
Background Art
[0002] CFC (chlorofluorocarbon) and HCFC (hydrochlorofluorocarbon), which have been conventionally
used as refrigerants for refrigeration equipment, have been subject to regulation
due to the problem of recent ozone depletion, and HFC (hydrofluorocarbon) has come
to be used as a refrigerant instead of them.
[0003] Among HFC refrigerants, HFC-134a, R407C, and R410A are normally used as refrigerants
for car air-conditioners, cold storage chambers, or room air-conditioners. Although
the ozone depletion potential (ODP) of these HFC refrigerant is zero, these come to
be subject to regulation, because the global warming potential (GWP) thereof is high.
While difluoromethane has been studied as one of alternate candidates of these refrigerants,
difluoromethane has the following problems: the global warming potential thereof is
not sufficiently low; the boiling point thereof is so low that thermodynamic characteristics
cannot be applied to a current refrigeration system directly; and difluoromethane
is not easily compatible with lubricating oils (refrigerating machine oils) used for
conventional HFC refrigerants, such as polyol esters and polyvinyl ethers. On the
other hand, unsaturated hydrofluorocarbons have been proposed to be used as a refrigerant
due to the following reasons; both of its ODP and GWP are very low; unsaturated hydrofluorocarbons
are non-flammable depending on structures; and in particular with respect to HFO-1234yf,
thermodynamic characteristics as measures of refrigerant performances are comparable
with or better than those of HFC-134a (Patent Literatures 1 to 3).
WO2011/163117A1 and
US2010/038582A1 also disclose working fluid compositions for refrigerating machines.
Citation List
Patent Literature
Summary of Invention
Technical Problem
[0005] In the case where a refrigerant and a refrigerating machine oil are applied to a
refrigeration system, it is demanded for the refrigerant that the refrigerant does
not have any adverse influences on the environment and that thermodynamics characteristics
are adapted to the refrigeration system. In addition, in a circumstance of coexistence
of the refrigerant and the refrigerating machine oil it is demanded that they are
soluble in each other (compatibility) and are excellent in thermal/chemical stability,
and that an oil film is maintained in order to suppress wear of a sliding member (lubricity).
[0006] With respect to a refrigeration system using unsaturated hydrofluorocarbons, it has
been considered that since refrigerating machine oils used in HFC, such as polyol
esters and polyvinyl ethers, exhibit compatibility with unsaturated hydrofluorocarbons,
these refrigerating machine oil can be applied. According to the studies by the present
inventors, however, the following problem has been revealed: unsaturated hydrofluorocarbons
have unstable double bonds in their molecules and thus are poor in thermal/chemical
stability.
[0007] In addition, one reason why the compatibility between the refrigerant and the refrigerating
machine oil (hereinafter, sometimes simply referred to as "compatibility".) is demanded
is because a refrigerating machine oil for lubricating a refrigerant compressor circulates
together with a refrigerant in the refrigerant circulation cycle of refrigeration
equipment. That is, in the refrigeration equipment, sufficient compatibility between
the refrigerant and the refrigerating machine oil is not achieved depending on the
selection of the refrigerating machine oil used to the refrigerant, and the refrigerating
machine oil discharged from the refrigerant compressor easily remains in the cycle.
As a result, there occur problems of wear due to lubrication failure by the reduction
in amount of the oil in the refrigerant compressor and of blockage of an expansion
mechanism such as a capillary. Therefore, it is important to select the refrigerating
machine oil adapted to the refrigerant. In a refrigeration system using difluoromethane,
however, a problem is that difluoromethane is not easily compatible with the refrigerating
machine oil, and there is also the problem of thermodynamics characteristics.
[0008] The present invention has been made in view of such problems, and an object thereof
is to provide a working fluid composition for a refrigerating machine that can achieve
compatibility and thermal/chemical stability in a refrigeration system using a refrigerant
which contains a hydrofluoroethane, difluoromethane and an unsaturated hydrofluorocarbon
without requiring for a significant modification of an existing system.
Solution to Problem
[0009] The present inventors have made intensive studies in order to achieve the above object,
and as a result, have found that by using a refrigerant containing a specific hydrofluoroethane,
difluoromethane and a specific unsaturated hydrofluorocarbon, and a refrigerating
machine oil of a specific ester or ether as a base oil, both of sufficiently high
compatibility and thermal/chemical stability can be achieved at high levels, leading
to the completion of the present invention.
[0010] That is, the present invention provides a working fluid composition for a refrigerating
machine in accordance with claim 1.
[0011] It is preferable that the refrigerant comprise 5 to 40 parts by mass of the hydrofluoroethane,
20 to 60 parts by mass of difluoromethane and 20 to 70 parts by mass of tetrafluoropropene
based on 100 parts by mass of the refrigerant.
[0012] It is preferable that a mass ratio of the refrigerant to the refrigerating machine
oil be 90 : 10 to 30 : 70.
[0013] It is preferable that the hydrofluoroethane be 1,1,1,2-tetrafluoroethane and that
a global warming potential of the refrigerant be 500 or less.
[0014] The base oil comprises a polyol ester having a carbon/oxygen molar ratio of 2.5 or
more and 5.8 or less, wherein the polyol ester includes polyol esters obtainable by
synthesis from fatty acids having 4 to 9 carbon atoms and polyhydric alcohols having
4 to 12 carbon atoms.
[0015] In the case where the base oil comprises a polyalkylene glycol having a carbon/oxygen
molar ratio of 2.5 or more and 5.8 or less, preferable examples of the polyalkylene
glycol compound include a compound having a homopolymerization chain of propylene
oxide or a copolymerization chain of propylene oxide and ethylene oxide, in which
at least one of both ends of the chain is blocked by an ether bond.
[0016] In the case where the base oil comprises a polyvinyl ether having a carbon/oxygen
molar ratio of 2.5 or more and 5.8 or less, preferable examples of the polyvinyl ether
include polyvinyl ethers having a structural unit represented by the following formula
(1).

[R
1, R
2 and R
3 may be the same or different and each represent a hydrogen atom or a hydrocarbon
group having 1 to 8 carbon atoms, R
4 represents a divalent hydrocarbon group having 1 to 10 carbon atoms or an ether bond
oxygen-containing divalent hydrocarbon group having 2 to 20 carbon atoms, R
5 represents a hydrocarbon group having 1 to 20 carbon atoms, m represents a number
such that an average value of m in the polyvinyl ether is 0 to 10, R
1 to R
5 may be the same or different in each occurrence of the structural units, and when
m represents 2 or more in one structural unit, a plurality of R
4O may be the same or different.]
Advantageous Effects of Invention
[0017] The present invention can provide a working fluid composition for a refrigerating
machine that can achieve compatibility and thermal/chemical stability in a refrigeration
system using a refrigerant which contains a hydrofluoroethane, difluoromethane and
an unsaturated hydrofluorocarbon without requiring for a significant modification
of an existing system.
Description of Embodiments
[0018] Hereinafter, a preferable embodiment of the present invention is described in detail.
[0019] A working fluid composition for a refrigerating machine according to an embodiment
of the present invention comprises
a refrigerant comprising a hydrofluoroethane represented by the following formula
(A), difluoromethane and tetrafluoropropene, and
a refrigerating machine oil comprising at least one selected from a polyol ester,
a polyvinyl ether and a polyalkylene glycol compound as a base oil, wherein a carbon/oxygen
molar ratio of the base oil is 2.5 or more and 5.8 or less.
C2HnF6-n (A)
[n represents 1 or 2.]
[0020] In the working fluid composition for a refrigerating machine according to the present
embodiment, the proportions of the refrigerant and the refrigerating machine oil blended
are not particularly limited, but the mass ratio of the refrigerant to the refrigerating
machine oil is preferably 90 : 10 to 30 : 70 and more preferably 80 : 20 to 40 : 60.
[0021] Then, the components contained in the working fluid composition for a refrigerating
machine are described in detail.
[Refrigerant]
[0022] The refrigerant in the present embodiment contains the hydrofluoroethane represented
by the above formula (A), difluoromethane and tetrafluoropropene.
[0023] Herein, the hydrofluoroethane represented by the above formula (A) is non-flammable.
Thus, as the ratio thereof blended is higher, the flammability is lower but the global
warming potential is higher. While no test method for evaluating the boundary between
"non-flammable" and "low flammable" is established and is being studied internationally,
the non-flammability of the mixed refrigerant is increased as the proportion of a
non-flammable compound is increased.
[0024] Difluoromethane (R32), whose pressure is high, increases the efficiency of the refrigerating
machine when the ratio thereof blended is high. But the GWP is increased and also
the compatibility of the refrigerant with the refrigerating machine oil is deteriorated,
when the ratio thereof blended is high.
[0025] On the other hand, tetrafluoropropene, whose global warming potential is extremely
low, is thus environmentally-friendly when the ratio thereof blended is high. But
it is poor in stability, and thus the stability of the working fluid is deteriorated
when the ratio thereof blended is high.
[0026] Then, in the present embodiment, the hydrofluoroethane represented by the above formula
(A), difluoromethane and tetrafluoropropene are mixed, and the resulting mixed refrigerant
can be used as a suitable refrigerant, in which disadvantages of the each refrigerants
are compensated and advantages thereof are utilized.
[0027] As the hydrofluoroethane represented by the above formula (A), 1,1,1,2-tetrafluoroethane
(HFC-134a) or pentafluoroethane (HFC-125) is preferable in terms of thermodynamics
characteristics. Furthermore, when the global warming potentials thereof are compared,
that of HFC-125 is 3400 while that of HFC-134a is 1300, and thus HFC-134a having a
lower GWP is more preferable. The hydrofluoroethane represented by the formula (A)
may be used singly or in combination of two or more.
[0028] Tetrafluoropropenes include 2,3,3,3-tetrafluoropropene (HFO-1234yf), 1,3,3,3-tetrafluoropropene
(HFO-1234ze), and 1,2,3,3-tetrafluoropropene (HFO-1234ye). Among them, HFO-1234yf
and HFO-1234ze are preferable, and in particular HFO-1234yf is preferable in terms
of physical properties of the refrigerant. Tetrafluoropropenes may be used singly
or in combination of two or more thereof.
[0029] The content of each of the refrigerants in the above refrigerant based on 100 parts
by mass of the refrigerant is preferably as follows: the content of the hydrofluoroethane
represented by the above formula (A) is 5 to 40 parts by mass, the content of difluoromethane
is 20 to 60 parts by mass, and the content of tetrafluoropropene is 20 to 70 parts
by mass; and more preferably as follows; the content of the hydrofluoroethane represented
by the above formula (A) is 10 to 30 parts by mass, the content of difluoromethane
is 20 to 60 parts by mass, and the content of tetrafluoropropene is 20 to 70 parts
by mass. Herein, difluoromethane is a high-pressure gas, and therefore when the content
thereof is high, the efficiency of the refrigerating machine is increased. But when
the content thereof is high, the GWP is increased, and also the compatibility between
the refrigerant and the refrigerating machine oil is deteriorated. On the other hand,
tetrafluoropropene, whose GWP is low, contributes environmental-friendliness when
the content thereof is high. But it is poor in stability and thus the stability of
the working fluid is deteriorated when the content thereof is high.
[0030] The global warming potential of the refrigerant (mixed refrigerant) in the present
embodiment is preferably 500 or less and more preferably 300 or less. Herein, the
global warming potential can also be reduced by mixing only difluoromethane and tetrafluoropropene
without using the hydrofluoroethane, but in such a case, the content of tetrafluoropropene
whose pressure is low is high. As a result, the efficiency of the refrigerating machine
cannot be increased and the stability is also poor.
[0031] While the refrigerant in the present embodiment can further contain a component other
than the above three components, the sum of the hydrofluoroethane represented by the
above formula (A), difluoromethane and tetrafluoropropene is preferably 80% by mass
or more and more preferably 90% by mass or more based on the total amount of the refrigerant.
[0032] The component other than the above three components includes a hydrofluorocarbon
(HFC) refrigerant other than the hydrofluoroethane represented by the above formula
(A), and a fluorine-containing ether-based refrigerant such as perfluoroethers.
[0033] In addition, the refrigerant in the present embodiment can further contain unsaturated
hydrofluorocarbons other than tetrafluoropropenes. As such unsaturated hydrofluorocarbons,
fluoropropenes containing 3 or 5 fluorine atoms are preferable, and any one of 1,2,3,3,3-pentafluoropropene
(HFO-1225ye) and 3,3,3-trifluoropropene (HFO-1243zf) or a mixture of two or more of
thereof is preferable. From the viewpoint of physical properties of the refrigerant,
HFO-1225ye is preferable.
[Refrigerating machine oil]
[0034] The refrigerating machine oil in the present embodiment contains a polyol ester and
optionally at least one selected from a polyvinyl ether and a polyalkylene glycol
compound as a base oil, and the carbon/oxygen molar ratio of the base oil is 2.5 or
more and 5.8 or less. Carbon and oxygen in the base oil can be quantitatively analyzed
by a common elemental analysis method. While a carbon analysis includes a thermal
conductivity method after conversion into carbon dioxide by burning, and a gas chromatography
method, an oxygen analysis is commonly a carbon reduction method in which carbon monoxide
derived by carbon is quantitatively analyzed, and a Shutze-Unterzaucher method is
widely put into practical use.
[0035] In the case where the base oil is a mixed base oil including two or more components,
the carbon/oxygen molar ratio of each of the components included in the mixed base
oil is not particularly limited as long as the carbon/oxygen molar ratio of the mixed
base oil is 2.5 or more and 5.8 or less, but it is preferable that the carbon/oxygen
molar ratio of each of the polyol ester, the polyvinyl ether and the polyalkylene
glycol compound be 2.5 or more and 5.8 or less. These preferable examples are described
later.
[Polyol ester]
[0036] The polyol ester is an ester obtainable by synthesis from a polyhydric alcohol and
a carboxylic acid, and the carbon/oxygen molar ratio is 2.5 or more and 5.8 or less,
preferably 3.2 or more and 5.0 or less, and further preferably 4.0 or more and 5.0
or less. As the carboxylic acid, fatty acids (aliphatic monocarboxylic acids), in
particular saturated fatty acids are used, and the number of carbon atoms thereof
is 4 or more and 9 or less and preferably 5 or more and 9 or less. The polyol ester
may be a partial ester in which some of hydroxyl groups in the polyhydric alcohol
remains as hydroxyl groups without being esterified, may be a complete ester in which
all of hydroxyl groups are esterified, or may be a mixture of the partial ester and
the complete ester; but the hydroxyl value is preferably 10 mgKOH/g or less, further
preferably 5 mgKOH/g or less, and most preferably 3 mgKOH/g or less.
[Fatty acid]
[0037]
(a) In the case where the proportion of difluoromethane that is poor in compatibility
with the refrigerating machine oil is high among main components of the refrigerant,
i.e., the hydrofluoroethane represented by the above formula (A), difluoromethane
and tetrafluoropropene, for example, in the case where the proportion of difluoromethane
in the refrigerant is 40% by mass or more, the proportion of branched fatty acids
of fatty acids forming the polyol ester is preferably 50 to 100% by mol, particularly
preferably 70 to 100% by mol, and further preferably 90 to 100% by mol.
Specific examples of branched fatty acids having 4 to 9 carbon atoms include branched
butanoic acids, branched pentanoic acids, branched hexanoic acids, branched heptanoic
acids, branched octanoic acids, and branched nonanoic acids. More specifically, fatty
acids branched at α-position and/or β-position are preferable, isobutanoic acid, 2-methylbutanoic
acid, 2-methylpentanoic acid, 2-methylhexanoic acid, 2-ethylpentanoic acid, 2-methylheptanoic
acid, 2-ethylhexanoic acid, 3,5,5-trimethylhexanoic acid, and the like are preferable,
and among them, 2-ethylhexanoic acid and/or 3,5,5-trimethylhexanoic acid is most preferable.
Herein, fatty acids other than branched fatty acids having 4 to 9 carbon atoms may
be included.
(b) In the case where the total of the content of tetrafluoropropene among main components
of the refrigerant is higher than the total of the contents of the hydrofluoroethane
represented by the above formula (A) and difluoromethane, the proportion of straight
fatty acids of fatty acids is preferably 50 to 95% by mol, particularly preferably
60 to 90% by mol, and further preferably 70 to 85% by mol in view of high compatibility
with the refrigerating machine oil.
[0038] Specific examples of straight fatty acids having 4 to 9 carbon atoms include butanoic
acid, pentanoic acid, hexanoic acid, heptanoic acid, octanoic acid, and nonanoic acid.
Among them, pentanoic acid and/or heptanoic acid is preferable, and in particular
a mixed acid thereof is most preferable. The content of straight pentanoic acid is
preferably 30% by mol or more in particular in terms of compatibility, and on the
other hand, is preferably 50% by mol or less and particularly preferably 45% by mol
or less in particular in terms of hydrolytic stability. The content of heptanoic acid
is preferably 20% by mol or more, particularly preferably 25% by mol or more, and
further preferably 30% by mol or more, in terms of lubricity. On the other hand, the
content is 50% by mol or less and preferably 45% by mol or less in particular in terms
of hydrolytic stability. As branched fatty acids other than straight fatty acids,
branched fatty acids having 5 to 9 carbon atoms, in particular, 2-ethylhexanoic acid
and/or 3,5,5-trimethylhexanoic acid is preferable. The content of 3,5,5-trimethylhexanoic
acid is preferably 5% by mol or more and particularly preferably 10% by mol or more
in particular in terms of hydrolytic stability, and on the other hand, the content
is preferably 30% by mol or less and particularly preferably 25% by mol or less in
particular in terms of compatibility and lubricity.
[0039] As preferable fatty acids in the cases (b), specifically, a mixed acid of straight
pentanoic acid, straight heptanoic acid and 3,5,5-trimethylhexanoic acid is preferable,
and this mixed acid is more preferably one containing 30 to 50% by mol of straight
pentanoic acid, 20 to 50% by mol of straight heptanoic acid and 5 to 30% by mol of
3,5,5-trimethylhexanoic acid.
[Polyhydric alcohol]
[0040] As the polyhydric alcohol forming the polyol ester, polyhydric alcohols having 2
to 6 hydroxyl groups are preferably used. The number of carbon atoms of polyhydric
alcohols is preferably 4 to 12 and particularly preferably 5 to 10. Hindered alcohols
such as neopentyl glycol, trimethylolethane, trimethylolpropane, trimethylolbutane,
di-(trimethylolpropane), tri-(trimethylolpropane), pentaerythritol and di-(pentaerythritol)
are preferable. Since being particularly excellent in compatibility with the refrigerant
and in hydrolytic stability, pentaerythritol or a mixed ester of pentaerythritol and
di-(pentaerythritol) is most preferable.
[Polyvinyl ether]
[0041] The carbon/oxygen molar ratio of the polyvinyl ether is preferably 2.5 or more and
5.8 or less, more preferably 3.2 or more and 5.8 or less, and further preferably 4.0
or more and 5.0 or less. If the carbon/oxygen molar ratio is less than this range,
hygroscopicity is higher, and if the ratio is more than this range, compatibility
is deteriorated. In addition, the weight average molecular weight of the polyvinyl
ether is preferably 200 or more and 3000 or less and more preferably 500 or more and
1500 or less.
[0042] The polyvinyl ether preferably used in the present embodiment has a structural unit
represented by the following formula (1).

[R
1, R
2 and R
3 may be the same or different and each represent a hydrogen atom or a hydrocarbon
group having 1 to 8 carbon atoms, R
4 represents a divalent hydrocarbon group having 1 to 10 carbon atoms or an ether bond
oxygen-containing divalent hydrocarbon group having 2 to 20 carbon atoms, R
5 represents a hydrocarbon group having 1 to 20 carbon atoms, m represents a number
such that an average value of m in the polyvinyl ether is 0 to 10, R
1 to R
5 may be the same or different in each occurrence of the structural units, and when
m represents 2 or more in one structural unit, a plurality of R
4O may be the same or different.]
[0043] At least one of R
1, R
2 and R
3 in the above formula (1) is preferably a hydrogen atom, and all thereof are particularly
preferably a hydrogen atom. m in the formula (1) is preferably 0 or more and 10 or
less, particularly preferably 0 or more and 5 or less, and further preferably 0. R
5 in the formula (1) represents a hydrocarbon group having 1 to 20 carbon atoms. This
hydrocarbon group includes an alkyl group, a cycloalkyl group, a phenyl group, an
aryl group, an arylalkyl group, and an alkyl group, and in particular an alkyl group
having 1 to 5 carbon atoms is preferable.
[0044] The polyvinyl ether in the present embodiment may be a homopolymer constituted by
one type of the structural unit represented by the formula (1) or a copolymer constituted
by 2 or more type of the structural units, but the copolymer brings about the effect
of further enhancing lubricity, insulation property, hygroscopicity, and the like
while satisfying compatibility. In this case, the types of monomers serving as raw
materials, the type of an initiator, and the rate of a copolymer can be selected to
thereby adapt the performances of an oil agent to the intended levels. Accordingly,
the following effect is exerted: an oil agent can be obtained at will according to
requirements such as lubricity and compatibility that vary depending on the type of
a compressor in a refrigeration system or an air-conditioning system, the material
of a lubrication portion, refrigeration ability, the type of a refrigerant, and the
like. The copolymer may be any of a block copolymer and a random copolymer.
[0045] In the case where the polyvinyl ether in the present embodiment is a copolymer, it
is preferable that the copolymer include a structural unit (1-1) represented by the
above formula (1) wherein R
5 represents an alkyl group having 1 to 3 carbon atoms, and a structural unit (1-2)
represented by the above formula (1) wherein R
5 represents an alkyl group having 3 to 20 carbon atoms, preferably 3 to 10 carbon
atoms, further preferably 3 to 8 carbon atoms. R
5 in the structural unit (1-1) is particularly preferably an ethyl group, and R
5 in the structural unit (1-2) is particularly preferably an isobutyl group. Furthermore,
in the case where the polyvinyl ether in the present embodiment is the copolymer including
the structural units (1-1) and (1-2), the molar ratio of the structural unit (1-1)
to the structural unit (1-2) is preferably 5 : 95 to 95 : 5, more preferably 20 :
80 to 90 : 10, and further preferably 70 : 30 to 90 : 10. In the case where the molar
ratio departs from the above range, there is a tendency toward insufficient compatibility
with the refrigerant and higher hygroscopicity.
[0046] The polyvinyl ether in the present embodiment may be one constituted by only the
structural unit represented by the above formula (1), but may be a copolymer further
including a structural unit represented by the following formula (2). In this case,
the copolymer may be any of a block copolymer and a random copolymer.

[R
6 to R
9 may be the same as or different from one another and each represent a hydrogen atom
or a hydrocarbon group having 1 to 20 carbon atoms.]
[End structure of polyvinyl ether]
[0047] The polyvinyl ether in the present embodiment can be produced by polymerization of
each corresponding vinyl ether-based monomer, and copolymerization of a corresponding
hydrocarbon monomer having an olefinic double bond with a corresponding vinyl ether-based
monomer. As the vinyl ether-based monomer corresponding to the structural unit represented
by the formula (1), a monomer represented by the following formula (3) is suitable.

[R
1, R
2, R
3, R
4, R
5 and m represent the same meaning as in R
1, R
2, R
3, R
4, R
5 and m in the formula (1), respectively.]
[0048] As the polyvinyl ether in the present embodiment, ethers having the following end
structures are suitable.
- (A) Those having a structure in which one end is represented by formula (4) or (5)
and other end is represented by formula (6) or (7).

[R11, R21 and R31 may be the same as or different from one another and each represent a hydrogen atom
or a hydrocarbon group having 1 to 8 carbon atoms, R41 represents a divalent hydrocarbon group having 1 to 10 carbon atoms or an ether bond
oxygen-containing divalent hydrocarbon group having 2 to 20 carbon atoms, R51 represents a hydrocarbon group having 1 to 20 carbon atoms, m represents a number
such that an average value of m in the polyvinyl ether is 0 to 10, and when m represents
2 or more, a plurality of R41O may be the same or different.]


[R61, R71, R81 and R91 may be the same as or different from one another and each represent a hydrogen atom
or a hydrocarbon group having 1 to 20 carbon atoms.]

[R12, R22 and R32 may be the same as or different from one another and each represent a hydrogen atom
or a hydrocarbon group having 1 to 8 carbon atoms, R42 represents a divalent hydrocarbon group having 1 to 10 carbon atoms or an ether bond
oxygen-containing divalent hydrocarbon group having 2 to 20 carbon atoms, R52 represents a hydrocarbon group having 1 to 20 carbon atoms, m represents a number
such that an average value of m in the polyvinyl ether is 0 to 10, and when m represents
2 or more, a plurality of R42O may be the same or different.]

[R62, R72, R82 and R92 may be the same as or different from one another and each represent a hydrogen atom
or a hydrocarbon group having 1 to 20 carbon atoms.]
- (B) Those having a structure in which one end is represented by the above formula
(4) or (5) and other end is represented by the following formula (8).

[R13, R23 and R33 may be the same as or different from one another and each represent a hydrogen atom
or a hydrocarbon group having 1 to 8 carbon atoms.]
[0049] Among such polyvinyl ether-based compounds, in particular the following is suitable
as a main component of the refrigerating machine oil of the present invention.
- (1) Those having a structure in which one end is represented by the formula (5) or
(6) and other end is represented by the formula (7) or (8), wherein in the formula
(1), R1, R2 and R3 are each a hydrogen atom, m represents a number of 0 to 4, R4 represents a divalent hydrocarbon group having 2 to 4 carbon atoms, and R5 represents a hydrocarbon group having 1 to 20 carbon atoms.
- (2) Those having only the structural unit represented by the formula (1), having a
structure in which one end is represented by the formula (5) and other end is represented
by the formula (7), wherein in the formula (1), R1, R2 and R3 are each a hydrogen atom, m represents a number of 0 to 4, R4 represents a divalent hydrocarbon group having 2 to 4 carbon atoms, and R5 represents a hydrocarbon group having 1 to 20 carbon atoms.
- (3) Those having a structure in which one end is represented by the formula (5) or
(6) and other end is represented by the formula (7) or (8), wherein in the formula
(1), R1, R2 and R3 are each a hydrogen atom, m represents a number of 0 to 4, R4 represents a divalent hydrocarbon group having 2 to 4 carbon atoms, and R5 represents a hydrocarbon group having 1 to 20 carbon atoms.
- (4) Those that are each of the (1) to (3), having a structural unit in which R5 in the formula (1) represents a hydrocarbon group having 1 to 3 carbon atoms, and
a structural unit in which such R5 represents a hydrocarbon group having 3 to 20 carbon atoms.
[Production of polyvinyl ether]
[0050] The polyvinyl ether in the present embodiment can be produced by subjecting the above
monomer to radical polymerization, cation polymerization, radiation polymerization,
or the like. After completion of the polymerization reaction, a usual separation/purification
method is if necessary conducted, and thus the intended polyvinyl ether-based compound
having the structural unit represented by the formula (1) is obtained.
[0051] As described above, it is required for the polyvinyl ether in the present embodiment
that the carbon/oxygen molar ratio is in the predetermined range, and the carbon/oxygen
molar ratio of a raw material monomer can be regulated to thereby produce a polymer
whose molar ratio is in the above range. That is, when the rate of a monomer whose
carbon/oxygen molar ratio is high is high, a polymer whose carbon/oxygen molar ratio
is high is obtained, and when the rate of a monomer whose carbon/oxygen molar ratio
is low is high, a polymer whose carbon/oxygen molar ratio is low is obtained. Herein,
in the case where a vinyl ether-based monomer and a hydrocarbon monomer having an
olefinic double bond are copolymerized, a polymer whose carbon/oxygen molar ratio
is higher than the carbon/oxygen molar ratio of the vinyl ether-based monomer is obtained,
but the proportion thereof can be regulated by the rate and the number of carbon atoms
of the hydrocarbon monomer having an olefinic double bond to be used.
[0052] In addition, in a production step of the polyvinyl ether represented by the above
formula (1), a side reaction may be caused and thus an unsaturated group such as an
aryl group may be formed in the molecule. If the unsaturated group is formed in the
polyvinyl ether molecule, the following phenomenon easily occurs: the thermal stability
of the polyvinyl ether itself is deteriorated, a polymerized produce is generated
to generate sludge, or antioxidative property (oxidation preventing property) is deteriorated
to generate peroxide. In particular, if peroxide is generated, it is decomposed to
generate a compound having a carbonyl group, and the compound having a carbonyl group
further generates sludge to easily cause blockage of a capillary. Therefore, as the
polyvinyl ether according to the present embodiment, those in which the degree of
unsaturation due to an unsaturated group and the like is low is preferable, and specifically,
the degree of unsaturation is preferably 0.04 meq/g or less, more preferably 0.03
meq/g or less, and most preferably 0.02 meq/g or less. In addition, the peroxide value
is preferably 10.0 meq/kg or less, more preferably 5.0 meq/kg or less, and most preferably
1.0 meq/kg. Furthermore, the carbonyl value is preferably 100 ppm by weight or less,
more preferably 50 ppm by weight or less, and most preferably 20 ppm by weight or
less.
[0053] Herein, the degree of unsaturation, the peroxide value and the carbonyl value in
the present invention are each the value measured by the Standard Methods for the
Analysis of Fats, Oils and Related Materials, established by the Japan Oil Chemists'
Society. That is, the degree of unsaturation in the present invention is the value
(meq/g) obtained by reacting a Wijs solution (ICl-acetic acid solution) with a sample,
leaving the resultant to stand in a dark area, thereafter reducing the excess ICI
to iodine, titrating the iodine content with sodium thiosulfate to calculate the iodine
value, and converting the iodine value to the vinyl equivalent; the peroxide value
in the present invention is the value (meq/kg) obtained by adding potassium iodide
to a sample, titrating the free iodine generated with sodium thiosulfate, and converting
the free iodine to the number of milliequivalents with respect to 1 kg of the sample;
and the carbonyl value in the present invention is the value (ppm by weight) obtained
by allowing 2,4-dinitrophenylhydrazine to act on a sample to yield a colorable quinoid
ion, measuring the absorbance of the sample at 480 nm, and converting the absorbance
to the carbonyl content based on a predetermined calibration curve with cinnamaldehyde
as the standard substance. The hydroxyl value is not particularly limited, but it
is desirable that the hydroxyl value be 10 mgKOH/g, preferably 5 mgKOH/g and further
preferably 3 mgKOH/g.
[Polyalkylene glycol compound]
[0054] The carbon/oxygen molar ratio of the polyalkylene glycol (PAG) compound in the present
embodiment is preferably 2.5 or more and 5.8 or less, preferably 2.5 or more and 4.0
or less, and further preferably 2.7 or more and 3.5 or less. If the molar ratio is
less than this range, hygroscopicity is high and electrical insulation property is
deteriorated, and if the molar ratio is more than this range, compatibility is deteriorated.
The weight average molecular weight of the polyalkylene glycol compound is preferably
200 or more and 3000 or less, and more preferably 500 or more and 1500 or less.
[Structural unit of polyalkylene glycol]
[0055] Polyalkylene glycols include those of various chemical structures, but a basic compound
thereof is polyethylene glycol, polypropylene glycol, polybutylene glycol, or the
like. The unit structure thereof is oxyethylene, oxypropylene, or oxybutylene, and
polyalkylene glycols can be obtained by subjecting each monomer, ethylene oxide, propylene
oxide, or butylene oxide, as a raw material, to ring-opening polymerization.
[Synthesis and end structure of polyalkylene glycol compound]
[0056] When a polyalkylene glycol compound is synthesized, an alcohol is often used as an
initiator, and a polymerized product (polymer) commonly has an ether bond with the
initiator at one end and a hydroxyl group (-OH) at the other end. A polyalkylene glycol
compound blocked at both end which is formed by blocking the hydroxyl group at the
other end by etherifying or esterifying, however, is lower in hygroscopicity than
the polyalkylene glycol compound in which a hydroxyl group remains. Herein, since
esters are hydrolyzed depending on conditions, a polyalkylene glycol compound whose
both ends each is an ether bond is preferable.
[0057] Examples of the polyalkylene glycol include a compound represented by the following
formula (9).
R
101-[(OR
102)
f-OR
103]
g (9)
[R
101 represents a hydrogen atom, an alkyl group having 1 to 10 carbon atoms, an acyl group
having 2 to 10 carbon atoms or a residue of a compound having 2 to 8 hydroxyl groups,
R
102 represents an alkylene group having 2 to 4 carbon atoms, R
103 represents a hydrogen atom, an alkyl group having 1 to 10 carbon atoms or an acyl
group having 2 to 10 carbon atoms, f represents an integer of 1 to 80, and g represents
an integer of 1 to 8.]
[0058] In the above formula (9), the alkyl group represented by each of R
101 and R
103 may be any of straight, branched and cyclic alkyl groups. The number of carbon atoms
of the alkyl group is preferably 1 to 10 and more preferably 1 to 6. If the number
of carbon atoms of the alkyl group is more than 10, compatibility with a working medium
tends to be deteriorated.
[0059] In addition, the alkyl group portion of the acyl group represented by each of R
101 and R
103 may be any of straight, branched and cyclic alkyl group portions. The number of carbon
atoms of the acyl group is preferably 2 to 10 and more preferably 2 to 6. If the number
of carbon atoms of the acyl group is more than 10, compatibility with a working medium
may be deteriorated to cause phase separation.
[0060] In the case where both of the groups represented by R
101 and R
103 are alkyl groups or acyl groups, the groups represented by R
101 and R
103 may be the same or different. Furthermore, when g represents 2 or more, a plurality
of R
101 and R
103 in the same molecule may be the same or different.
[0061] In the case where the group represented by R
101 is a residue of a compound having 2 to 8 hydroxyl groups, this compound may be a
chain group or may be a cyclic group.
[0062] In the polyalkylene glycol represented by the above formula (9), at least one of
R
101 and R
103 is preferably an alkyl group (more preferably an alkyl group having 1 to 4 carbon
atoms) and particularly preferably a methyl group in terms of compatibility with a
working medium.
[0063] Furthermore, both of R
101 and R
103 are preferably an alkyl group (more preferably alkyl groups having 1 to 4 carbon
atoms) and particularly preferably a methyl group in terms of thermal/chemical stability.
[0064] Preferably, any one of R
101 and R
103 is an alkyl group (more preferably an alkyl group having 1 to 4 carbon atoms) and
other thereof is a hydrogen atom, and particularly preferably, one is a methyl group
and other is a hydrogen atom, in terms of easiness of production and cost. In addition,
both of R
101 and R
103 are preferably a hydrogen atom in terms of lubricity and solubility of sludge.
[0065] R
102 in the above formula (9) represents an alkylene group having 2 to 4 carbon atoms,
and specific examples of such an alkylene group include an ethylene group, a propylene
group, and a butylene group. In addition, an oxyalkylene group as a repeating unit
represented by OR
102 includes an oxyethylene group, an oxypropylene group, and an oxybutylene group. Oxyalkylene
groups in the same molecule may be the same, and 2 or more oxyalkylene groups may
be included.
[0066] With respect to the polyalkylene glycol represented by the above formula (9), a copolymer
including an oxyethylene group (EO) and an oxypropylene group (PO) is preferable from
the viewpoints of compatibility with a working medium and viscosity-temperature characteristics,
and in this case, the proportion (EO/(PO+EO)) of the oxyethylene group in the sum
of the oxyethylene group and the oxypropylene group is preferably in a range from
0.1 to 0.8 and more preferably in a range from 0.3 to 0.6 in terms of baking load
and viscosity-temperature characteristics.
[0067] In addition, the value of EO/(PO+EO) is preferably in a range from 0 to 0.5, more
preferably in a range from 0 to 0.2, and most preferably 0 (namely, propylene oxide
homopolymer), in terms of hygroscopicity and thermal and oxidation stability.
[0068] In the above formula (9), f represents the number of repetitions of the oxyalkylene
group OR
102 (degree of polymerization), and represents an integer of 1 to 80. In addition, g
represents an integer of 1 to 8. For example, in the case where R
101 represents an alkyl group or an acyl group, g represents 1. In the case where R
101 represents a residue of a compound having 2 to 8 hydroxyl groups, g represents the
number of hydroxyl groups in the compound.
[0069] In addition, the product (f × g) of f and g is not particularly limited, but it is
preferable that the average value of f × g be 6 to 80 in order to satisfy the above-described
requirements and performances as the lubricating oil for a refrigerating machine in
a well-balanced manner.
[0070] The number average molecular weight of the polyalkylene glycol represented by the
formula (9) is preferably 500 to 3000, further preferably 600 to 2000 and more preferably
600 to 1500, and it is preferable that f represent a number so that the number average
molecular weight of the polyalkylene glycol satisfies the above conditions. In the
case where the number average molecular weight of the polyalkylene glycol is too low,
lubricity under coexistence with the refrigerant is insufficient. On the other hand,
in the case where the number average molecular weight is too high, a composition range
in which compatibility with the refrigerant is exhibited under low temperature conditions
is narrow, and lubrication failure in a refrigerant compressor and inhibition of heat
exchange in an evaporator easily occur.
[0071] The hydroxyl value of the polyalkylene glycol is not particularly limited, but it
is desirable that the hydroxyl value be 100 mgKOH/g or less, preferably 50 mgKOH/g
or less, further preferably 30 mgKOH/g or less, and most preferably 10 mgKOH/g or
less.
[0072] The polyalkylene glycol according to the present embodiment can be synthesized using
a conventionally known method ("
Alkylene Oxide Polymers", Shibata, M. et al., Kaibundo, issued on November 20, 1990). For example, the polyalkylene glycol represented by the above formula (9) is obtained
by performing addition polymerization of one or more predetermined alkylene oxides
to an alcohol (R
101OH; R
101 represents the same meaning as in R
101 in the above formula (9)), and subjecting the hydroxyl group at the end to etherification
or esterification. Herein, in the case where two or more different alkylene oxides
are used in the production step, the resulting polyalkylene glycol may be any of a
random copolymer and a block copolymer, but it is preferably a block copolymer because
of tending to be more excellent in oxidation stability and lubricity, and preferably
a random copolymer because of tending to be more excellent in low-temperature fluidity.
[0073] The kinematic viscosity at 100°C of the polyalkylene glycol according to the present
embodiment is preferably 5 to 20 mm
2/s, preferably 6 to 18 mm
2/s, more preferably 7 to 16 mm
2/s, further preferably 8 to 15 mm
2/s, and most preferably 10 to 15 mm
2/s. If the kinematic viscosity at 100°C is less than the above lower limit, lubricity
under coexistence with the refrigerant is insufficient, and on the other hand, if
the kinematic viscosity at 100°C is more than the above upper limit, a composition
range in which compatibility with the refrigerant is exhibited is narrow, and lubrication
failure in a refrigerant compressor and inhibition of heat exchange in an evaporator
easily occur. In addition, the kinematic viscosity at 40°C of the polyalkylene glycol
is preferably 10 to 200 mm
2/s and more preferably 20 to 150 mm
2/s. If the kinematic viscosity at 40°C is less than 10 mm
2/s, lubricity and sealability of a compressor tend to be deteriorated, and if the
kinematic viscosity at 40°C is more than 200 mm
2/s, a composition range in which compatibility with the refrigerant is exhibited under
low temperature conditions tends to be narrow, and lubrication failure in a refrigerant
compressor and inhibition of heat exchange in an evaporator tend to easily occur.
[0074] In addition, the pour point of the polyalkylene glycol represented by the above formula
(9) is preferably -10°C or lower and more preferably -20 to -50°C. If a polyalkylene
glycol having a pour point of -10°C or higher is used, the refrigerating machine oil
tends to be solidified at a low temperature in the refrigerant circulation system.
[0075] In addition, in the production step of the polyalkylene glycol of the above formula
(9), alkylene oxides such as propylene oxide may cause a side reaction and thus an
unsaturated group such as an aryl group may be formed in the molecule. If an unsaturated
group is formed in the polyalkylene glycol molecule, the following phenomenon easily
occurs: the thermal stability of the polyalkylene glycol itself is deteriorated, a
polymerized produce is generated to generate sludge, or antioxidative property (oxidation
prevention property) is deteriorated to generate peroxide. In particular, if peroxide
is generated, it is decomposed to generate a compound having a carbonyl group, and
the compound having a carbonyl group further generates sludge to easily cause blockage
of a capillary.
[0076] Accordingly, as the polyalkylene glycol according to the present embodiment, one
in which the degree of unsaturation due to an unsaturated group and the like is low
is preferable, and specifically, the degree of unsaturation is preferably 0.04 meq/g
or less, more preferably 0.03 meq/g or less, and most preferably 0.02 meq/g or less.
In addition, the peroxide value is preferably 10.0 meq/kg or less, more preferably
5.0 meq/kg or less, and most preferably 1.0 meq/kg. Furthermore, the carbonyl value
is preferably 100 ppm by weight or less, more preferably 50 ppm by weight or less,
and most preferably 20 ppm by weight or less.
[0077] In the present embodiment, in order to obtain a polyalkylene glycol in which the
degree of unsaturation, the peroxide value and the carbonyl value are low, it is preferable
that the reaction temperature at which propylene oxide is reacted be 120°C or lower
(more preferably 110°C or lower). In addition, if an alkali catalyst is used during
the production, an inorganic adsorbent such as activated carbon, activated white earth,
bentonite, dolomite, or aluminosilicate can be used for removing the catalyst, to
thereby reduce the degree of unsaturation. In addition, it is possible to prevent
the increase in peroxide value or carbonyl value also by avoiding the polyalkylene
glycol being in contact with oxygen as much as possible during its production or use,
or by adding an antioxidant.
[0078] While it is required for the polyalkylene glycol compound in the present embodiment
that the carbon/oxygen molar ratio is in a predetermined range, a polymer whose molar
ratio is in the above range can be produced by selecting and regulating the types
and the mixing ratio of the raw material monomers.
[0079] The content of the polyol ester, the polyvinyl ether or the polyalkylene glycol compound
in the refrigerating machine oil is preferably 80% by mass or more and particularly
preferably 90% by mass or more in total based on the total amount of the refrigerating
machine oil in order that the refrigerating machine oil is excellent in characteristics
demanded, such as lubricity, compatibility, thermal/chemical stability, and electrical
insulation property. As the base oil, a mineral oil, a hydrocarbon-based oil such
as an olefin polymer, a naphthalene compound and alkylbenzenes, and an oxygen-containing
synthetic oil such as carbonates, ketones, polyphenyl ethers, silicones, polysiloxanes
and perfluoroethers can be used in combination but the polyol ester, the polyvinyl
ether and the polyalkylene glycol compound described later,. As the oxygen-containing
synthetic oil, among them, carbonates or ketones are preferably used.
[0080] The kinematic viscosity of the refrigerating machine oil is not particularly limited,
but the kinematic viscosity at 40°C can be preferably set to 3 to 1000 mm
2/s, more preferably 4 to 500 mm
2/s, and most preferably 5 to 400 mm
2/s. In addition, the kinematic viscosity at 100°C can be preferably set to 1 to 100
mm
2/s and more preferably 2 to 50 mm
2/s.
[0081] The volume resistivity of the refrigerating machine oil is not particularly limited,
but it can be preferably set to 1.0 × 10
9 Ω·m or more, more preferably 1.0 × 10
10 Ω·m or more, and most preferably 1.0 × 10
11 Ω·m or more. In particular, in the case where the refrigerating machine oil is used
for a closed type refrigerating machine, a high electrical insulation property tends
to be required. In the present invention, the volume resistivity means the value at
25°C measured according to JIS C 2101 "Electrical Insulation Oil Test Method".
[0082] The moisture content in the refrigerating machine oil is not particularly limited,
but it can be preferably set to 200 ppm or less, more preferably 100 ppm or less,
and most preferably 50 ppm or less based on the total amount of the refrigerating
machine oil. In particular, in the case where the refrigerating machine oil is used
for a closed type refrigerating machine, the moisture content is demanded to be low
from the viewpoint of the influence on thermal/chemical stability and the electrical
insulation property of the refrigerating machine oil.
[0083] The acid value of the refrigerating machine oil is not particularly limited, but
it can be preferably set to 0.1 mgKOH/g or less and more preferably 0.05 mgKOH/g or
less in order to prevent corrosion of a metal used for a refrigerating machine or
a pipe, and to prevent decomposition of the ester contained in the refrigerating machine
oil according to the present embodiment. In the present invention, the acid value
means the acid value measured according to JIS K2501 "Petroleum Products And Lubricating
Oils-Neutralization Value Test Method".
[0084] The ash content of the refrigerating machine oil is not particularly limited, but
it can be preferably set to 100 ppm or less and more preferably 50 ppm or less in
order to increase the thermal/chemical stability of the refrigerating machine oil
according to the present embodiment and to suppress the occurrence of sludge or the
like. In the present invention, the ash content means the value of the ash content
measured according to JIS K2272 "Crude Oil/Petroleum Product Ash Content and Sulfated
Ash Content Test Method".
[0085] The working fluid composition for a refrigerating machine according to the present
embodiment can also be used in the form of being blended with various additives, if
necessary. While the content of the additives is shown based on the total amount of
a refrigerating machine oil composition, the content of these components in the fluid
composition for a refrigerating machine is preferably 5% by mass or less and particularly
preferably 2% by mass or less based on the total amount of a refrigerating machine
oil composition.
[0086] In order to further improve the wear resistance and the load resistance of the working
fluid composition for a refrigerating machine according to the present embodiment,
it is possible to blend at least one phosphorus compound selected from the group consisting
of phosphates, acidic phosphates, thiophosphates, amine salts of acidic phosphates,
chlorinated phosphates, and phosphites. These phosphorus compounds are esters of phosphoric
acid or phosphorous acid and an alkanol or a polyether type alcohol, or derivatives
thereof.
[0087] In addition, the working fluid composition for a refrigerating machine according
to the present embodiment can contain at least one epoxy compound selected from a
phenylglycidylether type epoxy compound, an alkylglycidylether type epoxy compound,
a glycidylester type epoxy compound, an allyloxysilane compound, an alkyloxysilane
compound, an alicyclic epoxy compound, an epoxidated fatty acid monoester and an epoxidated
vegetable oil in order to further improve the thermal/chemical stability thereof.
[0088] In addition, the working fluid composition for a refrigerating machine according
to the present embodiment can if necessary contain conventionally known additives
for a refrigerating machine oil in order to further enhance the performances thereof.
Examples of such additives includes a phenol-based antioxidant such as di-tert-butyl-p-cresol
and bisphenol A, an amine-based antioxidant such as phenyl-α-naphthylamine and N,N-di(2-naphthyl)-p-phenylenediamine,
a wear inhibitor such as zinc dithiophosphate, an extreme pressure agent such as chlorinated
paraffins and a sulfur compound, an oiliness agent such as fatty acids, a defoaming
agent such as silicones, a metal deactivator such as benzotriazole, a viscosity index
improver, a pour point depressant, and a detergent dispersant. These additives may
be used singly or in combination of two or more.
[0089] The working fluid composition for a refrigerating machine according to the present
embodiment is preferably used for a room air-conditioner and a cold storage chamber
having a closed type reciprocating or rotating compressor, or an open-type or closed
type car air-conditioner. In addition, the working fluid composition for a refrigerating
machine and the refrigerating machine oil according to the present embodiment are
preferably used for a cooling apparatus or the like of a dehumidifier, a water heater,
a refrigerator, a refrigeration and cooling warehouse, a vending machine, a showcase,
a chemical plant, or the like. Furthermore, the working fluid composition for a refrigerating
machine and the refrigerating machine oil according to the present embodiment are
also preferably used for one having a centrifugal compressor.
Examples
[0090] Hereinafter, the present invention is more specifically described based on Examples
and Comparative Examples, but the present invention is not limited to the following
Examples at all.
[Refrigerating machine oil]
[0091] First, 0.1% by mass of di-ter.-butyl-p-cresol (DBPC) as an antioxidant was added
to each of base oils 1 to 5 shown below to prepare each of refrigerating machine oils
1 to 5. Various properties of refrigerating machine oils 1 to 5 are shown in Table
1.
[Base oil]
[0092]
Base oil 1: ester of mixed fatty acid of 2-ethylhexanoic acid and 3,5,5-trimethylhexanoic
acid (mixing ratio (molar ratio): 50/50) with pentaerythritol. Carbon/oxygen molar
ratio: 4.8
Base oil 2: ester of mixed fatty acid of n-pentanoic acid, n-heptanoic acid and 3,5,5-trimethylhexanoic
acid (mixing ratio (molar ratio): 40/40/20) with pentaerythritol. Carbon/oxygen molar
ratio: 3.3
Base oil 3: ester of oleic acid and trimethylolpropane. Carbon/oxygen molar ratio:
9.8
Base oil 4: copolymer of ethyl vinyl ether and isobutyl vinyl ether (ethyl vinyl ether/isobutyl
vinyl ether = 7/1 (molar ratio)). Weight average molecular weight: 910; carbon/oxygen
molar ratio: 4.3
Base oil 5: compound in which both ends of polypropylene glycol were methyl-etherified.
Weight average molecular weight: 1100; carbon/oxygen molar ratio: 2.9
Base oil 6: compound being copolymer of polyoxyethylene glycol and polyoxypropylene
glycol, wherein one end was methyl-etherified. Weight average molecular weight: 1700;
carbon/oxygen molar ratio: 2.7

[Examples 1 to 4 and Comparative Examples 1 to 12]
[0093] In each of Examples 1 to 4 and Comparative Examples 1 to 12, with respect to each
working fluid composition for a refrigerating machine in which each of refrigerating
machine oils 1 to 6 was combined with each refrigerant shown in Tables 2 to 4, evaluation
tests shown below were performed. As described later, the mass ratio of the refrigerant
to the refrigerating machine oil in the working fluid composition for a refrigerating
machine was changed with respect to each test.
[0094] As the refrigerant, the followings were used. Mixed refrigerant A was set in favor
of refrigerant characteristics for the increase in efficiency, and the GWP thereof
was 500 or less, specifically 487. Mixed refrigerant B was set for a further reduction
in GWP, and the GWP thereof was 300 or less, specifically 288. Herein, HFC-134a, whose
GWP was as high as 1300, was currently used widely as a refrigerant, and therefore
used for comparison.
[Refrigerant]
[0095]
Mixed refrigerant A: HFC-134a/HFC-32/HFO-1234yf = 15/43/42 (mass ratio, GWP: 487)
Mixed refrigerant B: HFC-134a/HFC-32/HFO-1234yf = 10/23/67 (mass ratio, GWP: 288)
HFC-32: difluoromethane (GWP: 675)
HFO-1234yf: 2,3,3,3-tetrafluoropropene (GWP: 4)
HFC-134a: 1,1,1,2-tetrafluoroethane (GWP: 1300)
[0096] Then, with respect to each of the working fluid compositions for a refrigerating
machine in Examples 1 to 8 and Comparative Examples 1 to 12, evaluation tests shown
below were performed. The results are shown in Tables 2 to 4.
[Evaluation of compatibility]
[0097] According to JIS-K-2211, "Test Method of Compatibility of Refrigerating machine Oil
with Refrigerant", 2 g of each refrigerating machine oil was blended with 18 g of
each of the above refrigerants including the mixed refrigerants, and whether the refrigerant
and the refrigerating machine oil were dissolved in each other at 0°C or not was observed.
The results obtained are shown in Tables 2 to 4. In Tables, "Compatible" means that
the refrigerant and the refrigerating machine oil were dissolved in each other and
"Separated" means that the refrigerant and the refrigerating machine oil were separated
to two layers.
[Evaluation of thermal/chemical stability]
[0098] According to JIS-K-2211, 1 g of a refrigerating machine oil (initial ASTM color L:
0.5) in which the moisture content was adjusted to 100 ppm or less, 1 g of each of
various refrigerants described above, and a catalyst (wire of each of iron, copper
and aluminum) were enclosed into a glass tube, and then the resultant was placed in
a protective tube made of iron, and heated to 175°C and kept therein for one week.
After the test, the ASTM color of the refrigerating machine oil and the change in
color of the catalyst color were evaluated. The ASTM color was evaluated according
to ASTM D156. In addition, the change in color of the catalyst was evaluated by visually
observing the appearance for rating as no change, no gloss, or blackened. In the case
of no gloss or blackened, the mixed liquid of the refrigerating machine oil and the
refrigerant, namely, a working fluid can be said to be deteriorated. The results obtained
are shown in Tables 2 to 4.

Industrial Applicability
[0099] The present invention provides a working fluid composition for use in a refrigerating
machine which contains a refrigerant having a low GWP and containing a specific hydrofluoroethane,
difluoromethane and tetrafluoropropene, and the composition can be safely used as
a working fluid in a high-cooling efficiency refrigeration system having a compressor,
a condenser, a throttle device, an evaporator, and the like among which the refrigerant
is circulated, in particular, in a refrigerating machine having a compressor such
as a rotary-type, swing-type, or scrolling-type compressor, and can be suitably used
in the fields of a room air-conditioner, an all-in-one air conditioner, a coolerator,
a car air-conditioner, an industrial refrigerating machine, and the like, in which
lower flammability is demanded.