JP6324368B2 - Stabilized iodine carbon composition - Google Patents

Description

  This application is a US national phase application of PCT application PCT / US05 / 46982, filed December 21, 2005, claiming the benefit of priority of US provisional application 60 / 638,003, filed December 21, 2004. Each of which is a continuation-in-part of US application 11 / 795,779 filed on March 10, 1980, the entirety of which is incorporated herein by reference. This application also claims US application 12 / 467,061, filed May 15, 2009, which claims the benefit of priority of US provisional application 61 / 053,663, filed May 15, 2008 (see all of these). As a partial continuation application). This application is also a continuation-in-part of US application 13 / 022,902, filed February 8, 2011, which is a continuation of US application 11 / 937,267, filed November 8, 2007.

  Halogenated hydrocarbons find wide use in various industrial applications such as refrigerants, aerosol propellants, blowing agents, heat transfer media, and gaseous dielectrics. Many of these applications have previously used compositions containing major amounts of chlorofluorocarbon (CFC) and hydrochlorofluorocarbon (HCFC). However, environmental concerns of concern have become associated with the use of some of these halogenated hydrocarbons, for example, both CFCs and HCFCs tend to exhibit relatively high global warming potential . Thus, it has become desirable in many applications to use compositions that are suitable for the intended use, but at the same time have a lower global warming potential than CFCs and other undesirable halogenated compounds.

  Applicants have advantageously used some compositions containing iodinated compounds, particularly those containing trifluoroiodomethane, in cooling (and other) applications, many of which have a high global warming potential. It has been recognized that the various chlorinated compounds it has can reduce the potential for environmental damage caused by it. However, Applicants have found that iodinated compounds such as trifluoroiodomethane tend to be relatively unstable, often under some normal cooling conditions, often CFC, HCFC, and hydrofluorocarbons ( It was further recognized that the stability was much lower than HFC).

  In order to be useful as a refrigerant and as a replacement for other CFC, HCFC, and HFC fluids, suitable compositions containing iodinated compounds must be stable. Applicants have recognized that one possible method for producing a suitable stable iodine composition is to use stabilizing compounds therein.

  Various stabilizers are known for use with HCFC and CFC compositions. HFCs may or may not use stabilizers included in their compositions, as is known in the art, due to their very good stability. For example, US Pat. No. 5,380,449 discloses a composition comprising dichlorotrifluoroethane and a stabilizing amount of at least one phenol and at least one aromatic or fluorinated alkyl epoxide. However, since iodo compounds tend to be much less stable than CFCs and HCFCs, it is possible to stabilize iodo compounds to the extent that the same or similar compounds are sufficient to be used as CFC / HCFC substitutes. It cannot be predicted from the stabilizer teachings for CFCs and HCFCs (eg the '449 disclosure). That is, as will be appreciated by those skilled in the art, C—Cl and C—F bonds tend to be at least about 1.5-2 times stronger than C—I bonds. Therefore, it is essentially to expect that compounds that stabilize HCFCs or CFCs are suitable to make iodo compounds useful in refrigerant applications that need to add about twice the amount of stability. Is inevitably not valid.

  Thus, Applicants produce compositions comprising iodo compounds such as trifluoroiodomethane that are sufficiently stable for various applications such as as a replacement for CFC, HCFC, and HFC refrigerants. Recognized the need.

  In cooling applications, it has been proposed to use some iodocarbon compounds as an alternative to some CFCs and HCFCs used so far. For example, JP 09-059612 (Application No. 07-220964) discloses a refrigerant composition containing trifluoroiodomethane and one or more phenolic compounds. This patent document shows that the phenolic composition acts to stabilize trifluoroiodomethane against degradation.

US Pat. No. 5,380,449 Japan Open 09-059612

  Compositions that include phenolic compounds as stabilizers for trifluoroiodomethane may have some success, but in some applications either do not use phenolic compounds or use such compounds. It may be desirable to use a lower concentration. For example, phenols are generally acidic due to the dissociation of hydroxyl groups and are relatively reactive. These features may be undesirable in some applications and / or in some situations.

The present invention is surprisingly stable and various compositions comprising iodocarbon compounds such as trifluoroiodomethane (CF ₃ I) that can be used advantageously in various applications such as refrigerants in various cooling systems. I will provide a. In particular, Applicants have Unexpectedly, generally iodocarbon compounds, and _C 1 -C ₅ iodocarbons, and even more preferably _C 1 -C ₂ iodocarbon, especially (preferably _{C 1} iodocarbons Trifluoroiodomethane mixed with one or more stabilizer compounds selected from a set of specific compounds, such as cooling systems, especially for commercial, industrial and personal use. A very well stabilized iodocarbon-containing composition, preferably a trifluoroiodomethane-containing composition, suitable as a heat transfer fluid for use in air conditioning systems (including automotive air conditioning systems), etc. I found. Furthermore, the composition is not only sufficiently stable for various applications, but also tends to exhibit a unique combination of non-flammability and a combination of low ozone depleting and global warming properties. These are particularly useful candidate substances as replacements for CFC, HCFC, and HFC refrigerants.

  As used herein, the term “iodocarbon” includes at least one carbon-iodine bond and iodofluorocarbon (having at least one carbon-iodine bond and at least one carbon-fluorine bond, but not a carbon-carbon bond). Compounds having no other bonds), as well as hydroiodofluorocarbons (having at least one carbon-iodine bond, at least one carbon-fluorine bond, at least one carbon-hydrogen bond, but other than carbon-carbon bonds) It is intended to cover compounds that do not have a bond.

Accordingly, the present invention provides, in one aspect, at least one iodocarbon compound, preferably a C ₁ -C ₅ iodocarbons, the composition even more preferably containing C ₁ iodocarbon, and at least one stabilizing compound About. In some cases, the composition can include any one or more stabilizers based on free radical scavenging functions, but in many preferred embodiments, the stabilizer is one or more diene-based. , Some phenolic compounds, some epoxides, some phosphites, and some phosphates, preferably in at least a major proportion.

In some preferred embodiments, the diene-based compound is one or more isoprene-based compounds. As used herein, the term “diene-based compound” refers to both substituted and unsubstituted C ₃ -C ₅ compounds having two or more double bonds in the molecular structure, and such C ₃ -C ₅ compounds. Refers to a compound that can be formed by one or more reactions involving, provided that at least one double bond is present in such reaction product compound. In a preferred embodiment, the diene-based compounds of the invention include C ₃ -C ₂₀ compounds of substituted and unsubstituted having two or more double bonds in the molecular structure. As used herein, the term “isoprene-based compound” refers to an isopropene, a compound having an isoprene group, and a compound that can be formed by one or more reactions involving isoprene. For example, as defined herein, diene-based compounds include myrcene and farsenol, each of which has three carbon-carbon double bonds. Thus, the term “diene-based” is not limited to compounds having only two double bonds, but includes compounds having fewer or more than two carbon-carbon double bonds. In the case of a diene-based compound formed by a combination of multiple C ₃ -C ₅ dienes, the combined molecules may be the same or different.

  Applicants have found that under some conditions of use, iodocarbon compounds are present in the presence of lubricants, particularly in the presence of lubricant compounds, and even more particularly under the temperature conditions experienced by refrigerants in vapor compression cycle operation. Below, it has been recognized that they tend to be generally less stable than compounds having C—Cl and C—F bonds instead of C—I bonds. Thus, Applicants have identified iodine, such as trifluoroiodomethane, that is sufficiently stable for a variety of applications, such as heat transfer applications, such as refrigerants, and even more preferably substitutes for CFC and HCFC refrigerants. It has been recognized that it would be desirable to provide a composition comprising a carbon compound. Such compositions offer the potential to reduce the environmental damage that would be caused when using CFC and HCFC based compositions instead of the compositions of the present invention. However, Applicants have found that iodinated compounds generally tend to be relatively unstable and, under some usage conditions, such as those present in normal cooling systems, are often more than CFCs and HCFCs. Also recognized that the stability is very low. For example, after performing standard recommended ASHRAE and SAE tests on various refrigerants, the inventors have found that compounds containing iodofluorocarbons produce brown / black iodine, which is in the test conditions. It is thought that it was formed from the decomposition of iodofluorocarbons.

The inventors have unexpectedly discovered that at least one stable iodocarbon compound, preferably a C ₁ -C ₂ iodocarbon, more preferably a C ₁ iodocarbon, and even more preferably trifluoroiodomethane. Compound, preferably a compound having a free radical scavenging function, even more preferably (1) a diene-based compound, preferably a diene-based compound having at least 2 carbon-carbon double bonds and at least 4 carbon atoms (2) epoxy compounds, for example, preferably the following formulas (E1) and (E2):

(Where
R ¹ is an aliphatic group having at least 3 carbon atoms, preferably at least 4 carbon atoms, and more preferably in some embodiments, R ¹ is a non-cyclic group having 4 to 6 carbon atoms. A saturated aliphatic group, and in some highly preferred embodiments, R ¹ is a 4-carbon unsaturated aliphatic group;
R ² is an aliphatic group having 4 or 5 carbon atoms, or a polycyclic aromatic group, preferably a naphthyl group, and combinations thereof)
An epoxy compound selected from substituted or unsubstituted compounds according to:
(3) The following formula P1:

Wherein each R is independently a phenyl group or a carboxylate group having at least 6 but less than 15 carbon atoms.
Phosphite according to
(4) non-hindered or weakly hindered phenols (the term is defined below); and any combination of two or more thereof;
It was found that it can be mixed with at least one compound selected from the group consisting of:

  As used herein, the term weakly hindered phenol means that there are aliphatic substituents at the 2 and 6 positions on the phenol ring and the total number of carbon atoms in the substituents at these positions is greater than 4 but less than 8. Means a substituted phenol. In a preferred embodiment, the total number of substituent carbon atoms at the 2 and 6 positions is 5 or 6, even more preferably 5. As used herein, the term non-hindered phenol refers to a phenol having a total number of carbon atoms totaling 2 or less in any combination of substituents present on either the 2 or 6 position on the phenol ring. Means.

  In some highly preferred embodiments, the stabilizing compound used in accordance with various aspects of the present invention is (1) a diene-based compound, preferably at least 2 carbon-carbon double bonds and at least 4 carbons. Diene-based compounds having atoms; (2) epoxy compounds, for example, preferably the following formulas (E1) and (E2):

(Where
R ¹ is an aliphatic group having at least 3 carbon atoms, preferably at least 4 carbon atoms, and more preferably in some embodiments, R ¹ is a non-cyclic group having 4 to 6 carbon atoms. A saturated aliphatic group, and in some highly preferred embodiments, R ¹ is a 4-carbon unsaturated aliphatic group;
R ² is an aliphatic group having 4 or 5 carbon atoms, or a polycyclic aromatic group, preferably a naphthyl group, and combinations thereof)
An epoxy compound selected from substituted or unsubstituted compounds according to:
(3) The following formula P1:

Wherein each R is independently a phenyl group or a carboxylate group having at least 6 but less than 15 carbon atoms.
A phosphite according to: and any combination of two or more thereof;
Comprising at least one compound selected from the group consisting of, preferably in a major proportion, more preferably in some embodiments substantially consisting thereof.

Furthermore, the compositions are not only sufficiently stable for various applications, but also tend to exhibit a unique combination of nonflammability and low ozone depleting properties, which makes them heat transfer. It is particularly useful as a fluid, especially as an alternative to currently used refrigerants, such as CFC and HCFC refrigerant substitutes. Furthermore, the Applicants have found that many advantages according to the present invention include, in addition to iodocarbons, preferably stabilizers, especially HFCs, preferably C ₁ -C ₄ HFCs, and halogenated olefins, preferably C _2. found that can be achieved for -C ₅ halogenated olefins one or more other compounds compositions also comprising such.

  Applicants have further recognized that preferred compositions of the present invention are stable and suitable for use in many systems, devices, and methods. For example, one form of the present invention is a system, apparatus comprising a composition of the present invention that is included as a heating or cooling fluid (based on latent and / or sensible heat transfer), particularly in cooling applications such as automotive air conditioning applications. And a method. Other systems, devices, and methods are also within the scope of the invention, as described more fully below.

  In yet another aspect, the present invention preferably comprises a stabilizer preferably comprising one or more preferred stabilizing compounds as referred to herein, including in many preferred embodiments diene-based compounds according to the present invention. Provides methods, systems, and apparatus for stabilizing compositions comprising at least one iodocarbon compound.

DESCRIPTION OF PREFERRED EMBODIMENTS Composition-Overview:
Preferred compositions are at least one iodocarbon, preferably a C ₁ iodofluorocarbon (such as trifluoroiodomethane (CF ₃ I)), and preferably at least one stabilizer, preferably a diene-based compound. One or more preferred stabilizing compounds referred to herein, such as in an amount effective to stabilize the iodocarbon against degradation under the conditions of use.

Some preferred compositions of the present invention, the iodocarbon, and at least one saturated HFC and / or at least one haloalkene, preferably 1 or more HFC of C ₁ -C _4, and / or one or more Of C ₂ -C ₅ haloalkenes.

If the haloalkenes such exists, haloalkene preferably, C ₂ -C ₄ haloalkene, even more preferably at least two, preferably a C ₂ -C ₄ haloalkene with at least three fluorine substituents. Of such haloalkenes, highly preferred for use in connection with heat transfer applications such as automotive air conditioning, in particular, are tetrafluoropropenes, especially 2,3,3,3-tetrafluoropropene (HFO- 1234yf). In some such preferred embodiments, the composition comprises from about 5 wt% to about 50 wt% iodocarbon, more preferably from about 20 wt% to about 40 wt%, based on the combined weight of iodocarbon and haloalkene. iodocarbons, and even more preferably about 25% to about 35% of iodocarbon, and from about 50% to about 95% by weight of HFC, especially the _C 1 -C ₄ HFC, and / or halogenated olefins, preferably C ₂ -C ₅ halogenated olefin, even more preferably C ₂ -C ₄ haloalkene, more preferably about 60 wt% to about 80 wt% HFC, preferably C ₁ -C ₄ HFC, and / or halogenated olefins, preferably _C 2 -C ₅ halogenated olefins, even more preferably _C 2 -C ₄ haloalkene, and even more preferably 65% to about 75% of HFC, preferably _C 1 -C ₄ of HFC, and / or halogenated olefins, preferably _C 2 -C ₅ halogenated olefin, even more preferably a haloalkene.

Some preferred compositions of the invention comprise iodocarbon, and at least one _C 1 -C ₄ of HFC, preferably the _C 1 -C ₃ of HFC, and even more preferably _C 1 -C ₂ of HFC . In some such preferred embodiments, the composition comprises from about 50% to about 95% iodocarbon, more preferably from about 65% to about 85% iodocarbon, based on the combined weight of iodocarbon and HFC. And about 5% to about 50% HFC, and even more preferably about 15% to about 35% HFC.

  In preferred embodiments, the composition has a global warming potential (GWP) of about 1000 or less, more preferably about 500 or less, even more preferably about 150 or less, and in some cases about 100 or less. In some embodiments, the composition has a GWP of about 75 or less. As used herein, “GWP” is defined in “The Scientific Assessment of Ozone Depletion, 2002, a report of the World Meteorological Association's Global Ozone Research and Monitoring Project” (incorporated herein by reference). It is measured over a 100 year target period relative to that of carbon dioxide.

  Preferably, the composition also has an ozone depletion potential (ODP) of about 0.05 or less, more preferably about 0.02 or less, and even more preferably about zero. As used herein, “ODP” is defined in “The Scientific Assessment of Ozone Depletion, 2002, A report of the World Meteorological Association's Global Ozone Research and Monitoring Project” (incorporated herein by reference). That's right.

A. Iodocarbon:
In view of the teachings contained herein, it is contemplated that the iodocarbon compounds according to the present invention may include one or more of a wide range of such compounds. For example, in some preferred embodiments, iodocarbon _compound, C 1 -C ₆ iodocarbons are intended to even more preferably _C 1 -C ₃ iodofluorocarbon. The iodocarbon may contain carbon, hydrogen, fluorine, and iodine.

In some preferred compositions of the present invention, iodocarbon, C ₁ -C ₃ iodocarbons, more preferably C ₁ iodocarbons, and even more preferably from C ₁ iodofluorocarbon. In some highly preferred embodiments, the at least one iodocarbon compound comprises trifluoroiodomethane (CF ₃ I), preferably in a major proportion based on the total iodocarbon compound. Thus, in some highly preferred embodiments, the composition comprises at least one C ₁ compound that includes only carbon-fluorine bonds and carbon-iodine bonds, at least two carbon-fluorine bonds, and at least Even more preferred are C ₁ compounds containing one carbon-iodine bond.

  Trifluoroiodomethane is readily available from various commercial sources such as Matheson TriGas, Inc. Furthermore, trifluoroiodomethane produced by any of various conventional methods can be used. An example of one such conventional method for producing trifluoroiodomethane is JACS 72,3806 (1950), “The Degradation of Silver Trifluoroacetate to Trifluoroiodomethane”, Albert L. Henne and William G. Finnegan (herein incorporated by reference). Inclusive).

  In general, the iodocarbon compound can be present in the composition in a wide range of amounts depending on a number of factors such as, for example, the particular intended use conditions of the compound. In some preferred embodiments, the one or more iodocarbon compounds are present in the composition in an amount of from about 5% to less than about 100%, more preferably from about 20% to less than about 100%, by weight. To do. In some preferred embodiments, particularly those in which the composition comprises one or more HFCs, the one or more iodocarbon compounds are from about 5% to about 35%, more preferably from about 45%, by weight. It is present in the composition in an amount of about 95%, even more preferably 65% to about 95%. In some preferred embodiments, particularly where the composition comprises one or more halogenated alkenes, the one or more iodocarbon compounds are about 15% to about 50%, more preferably about 20%, by weight. Present in the composition in an amount of from about 40%, even more preferably from about 25% to about 35%.

  With respect to the relative weight of the one or more iodocarbon compounds and the stabilizer, in some embodiments, the iodocarbon is based on the total weight of the iodocarbon and stabilizer, preferably a diene-based compound, in the composition. As from about 90% to about 99.999%, more preferably from about 95% to about 99.99%, even more preferably from about 96% to about 99.7% by weight.

B. One or more stabilizers:
In some preferred embodiments, the stabilizer compound is about 0.001 wt% to about 15 based on the total weight of the composition, preferably a composition comprising iodocarbon, more preferably a refrigerant composition comprising iodocarbon. Compositions in an amount of about wt%, more preferably about 0.01 wt% to about 10 wt%, even more preferably about 0.3 wt% to about 5 wt%, even more preferably about 1 to about 2 wt%. Present in. In some cases, the stabilizer compound is about 0.001 wt% to about 15 wt%, more preferably about 0.01 wt% to about 10 wt%, based on the total weight of lubricant and stabilizer, Even more preferably, it is present in the composition in an amount of from about 0.3% to about 5%, even more preferably from about 1 to about 2% by weight. In some preferred embodiments, the stabilizer compound is present in an amount of about 0.5% to about 2% by weight, based on the total weight of the composition, preferably the compound comprising iodocarbon.

1. One or more diene-based compounds:
Any one or more available diene-based compounds can be adapted for use in accordance with the present invention, and one of ordinary skill in the art will be able to do without undue experimentation in light of the teachings contained herein. It will be appreciated that the number and type of such compound (s) appropriate for any particular application can be selected. The type and nature of the one or more diene-based compounds used is, at least to some extent, the one or more specific iodocarbon compounds used in the composition, the expected use conditions of the composition, and related There is a possibility that it will be decided by the factor to do.

In general, the amount of diene-based stabilizer used in the composition of the present invention will depend on factors such as the type of iodocarbon in the composition and the expected use conditions of the composition, among other factors. It can be widely changed. In general, it is preferred to use an effective amount of diene-based stabilizer for the iodocarbon used. As used herein, the term “effective amount” refers to a composition containing a related iodocarbon compound such as trifluoroiodomethane, as compared to the same composition without a diene-based compound. Refers to the amount of one or more diene-based compounds that provides a stabilized composition in which the iodocarbon decomposes more slowly and / or to a lesser extent under the same or similar conditions. In the particular example of trifluoroiodomethane, one important degradation product is trifluoromethane, which is formed by replacing iodine in the CF ₃ I molecule with hydrogen. Similarly, iodine may be replaced with hydrogen in other iodocarbons, thereby forming compounds that may have relatively high GWP values, eg, values greater than 150. These decomposition products have the effect of increasing the GWP of the refrigerant blend using iodocarbon. Therefore, the goal of giving a low global warming potential cannot be achieved. Preferably, the effective amount of stabilizer reduces the amount of iodocarbon decomposition so that the GWP of the refrigerant composition is less than 1000, and even more preferably less than 150. Even without considering the GWP value, it is not desirable that the components of the refrigerant composition be decomposed. Accordingly, the level of decomposition products described above may be less than 2.0% by weight of the total refrigerant composition, more preferably less than about 1.0% by weight, and even more preferably less than about 0.5% by weight. preferable. In some preferred embodiments, this amount of one or more diene-based compounds is in accordance with standard testing of SAE-J1662 (published June 1993) and / or ASHRAE-97-1983R (published 1997). A stabilized composition that, when tested, decomposes more slowly and / or to a lesser extent when compared to the same composition that does not contain a diene-based compound, at least one iodocarbon compound therein. Is enough to give. For example, in some preferred embodiments, the amount of decomposition product, i.e., the product formed by replacing iodine in the iodocarbon with hydrogen, is maintained after holding the composition at about 300 <0> F for about 2 weeks. Less than about 0.9% by weight, even more preferably less than about 0.7% by weight.

The diene-based compounds of the present invention may be cyclic or acyclic compounds, and in many embodiments acyclic compounds are generally preferred. Acyclic diene-based compounds of the for use in the present invention are _preferably, C 5 _{-C 30} diene-based compound, more preferably _C 5 _{-C 20} diene-based compound, even more preferably _C 5 -C _{A 15} diene based compound. With respect to the cyclic diene-based compound, the compound may be an aromatic or non-aromatic compound, with non-aromatic diene-based cyclic compounds being preferred in some embodiments.

  In preferred embodiments, the diene-based compounds are allyl ethers, propadiene, butadiene, terpenes (such as myrcene, farnesene, and limonene), and isopropene-based (such as terpene derivatives (such as farnesol and geraniol)). As well as any combination of two or more thereof. As used herein, each of the compounds defined in the immediately preceding list is intended to encompass both substituted and unsubstituted forms of the defined compound. In some preferred embodiments, the diene-based compound comprises a major proportion of propadiene, and even more preferably consists essentially of it.

In some other preferred embodiments, the diene-based compound comprises a major proportion of terpenes, terpene derivatives, or combinations thereof, and even more preferably is practically composed thereof. As used herein, the term “terpene” means a compound containing at least 10 carbon atoms and containing at least one, preferably at least two isoprene groups. In many preferred embodiments, the terpene compound of the present invention is a reaction of at least two isoprene C ₅ units (CH ₂ ═C (CH ₃ ) —CH═CH ₂ ), each unit being substituted or unsubstituted. Thus, many of the terpene compounds of the present invention preferably have at least 10 carbon atoms and contain at least one isoprene group. The term “isoprene group” as used herein refers to any portion of a molecule that contains a group that can be formed from substituted or unsubstituted isoprene. In some preferred embodiments, unsubstituted terpenes are preferred.

In many preferred embodiments, the terpene compounds of the present invention comprise at least one head-to-tail condensation product of a modified or unmodified isoprene molecule. Any one or more terpene compounds can be adapted for use in accordance with the present invention, and those skilled in the art will be able to use any particular application without undue experimentation in light of the teachings contained herein. It is contemplated that the number and type of one or more terpene compounds may be selected for. Preferred terpenes of the present invention are cyclic or acyclic, saturated or unsaturated, substituted or unsubstituted hydrocarbons having the molecular formula (C ₅ H ₈ ) _n , where n is preferably 2 to 2 About 6, even more preferably 2-4. Terpenes according to the invention having the formula: C ₁₀ H ₁₆ (including substituted forms) are sometimes referred to herein as monoterpenes, whereas terpenes having the formula: C ₁₅ H ₂₄ (including substituted forms) Are sometimes referred to herein as sesquiterpenes. Terpenes of the present invention having the formula: C ₂₀ H ₃₂ (including substituted forms) are sometimes referred to herein as diterpenes, while terpenes having the formula: C ₃₀ H ₂₄ (including substituted forms). Is sometimes called a triterpene, and many others. Terpenes containing 30 or more carbons are usually formed by condensing two terpene precursors in a regular pattern. Although it is contemplated that all such terpenes can be adapted for use in accordance with the present invention, it is generally preferred to use monoterpenes.

  In some preferred embodiments, the one or more terpene compounds of the composition comprise one or more acyclic terpene compounds, preferably in a major proportion, and still more preferably consist substantially of it. The Among acyclic terpenes, it is believed that such compounds may be within the class of compounds identified as head-to-tail isoprenoids, or classes of compounds that are not so bound. Preferred acyclic terpenes for use in accordance with some aspects of the present invention include myrcene (2-methyl-6-methyleneocta-1,7-diene), allo-cymene, β-oscymene.

  In some embodiments, the terpene compound of the present invention may comprise a cyclic terpene compound. Among cyclic terpenes, monocyclic, bicyclic, tricyclic, or tetracyclic compounds with various degrees of unsaturation are intended for use in accordance with the present invention.

Examples of terpene compounds that can be adapted for use in connection with the various forms of the present invention include terbene, myrcene, limonene, retinal, pinene, menthol, geraniol, farnesol, phytol, vitamin A ₁ , terpinene, δ-3 carene , Terpinolene, ferrandlene, fenchen and the like, and blends thereof (including all these isomers).

  In some preferred embodiments, the terpene compound of the composition comprises one or more sesquiterpenes, preferably farnesol and / or farnesene. The term “farnesol” is a compound of 3,7,11-trimethyl-2,6,10-dodecatrien-1-ol, including all its stereoisomers. Farnesol is a sesquiterpene alcohol found as a colorless liquid and is a natural organic compound that is insoluble in water but miscible with oil. This is the chemical structure:

Have The term “farnesene” refers to α-farnesene (ie, 3,7,11-trimethyldoscadedodec-1,3,6,19-tetraene) and β-farnesene (ie, 7,11-dimethyl-3-methylene). -1,6,10-dodecatriene) (including all these stereoisomers).

  Examples of terpene derivatives according to the invention include oxygen-containing derivatives of terpenes such as alcohols, aldehydes or ketones containing hydroxyl or carbonyl groups, as well as hydrogenated derivatives. Oxygen-containing derivatives of terpenes are sometimes referred to herein as terpenoids. In some embodiments, the diene-based compound of the present invention comprises a terpenoid carnosic acid. Carnosic acid is a phenolic diterpene corresponding to empirical formula C2028O4. It is naturally produced in plants of the Libiatae family. For example, carnosic acid is a constituent of Salvia officinalis species (sage) and Rosmarinus officinalis species (rosemary) and is found primarily in leaves. Carnosic acid is also found in thyme and marjolan (Linde (Helb. Chim. Acta, 1234 (1962)) for Salvia officinalis) and Wenkert et al. (J. Org. Chem., 30, 2931 (for Rosmarinus officinalis). 1965))), and also in various other sage species (for Salvia canariensis, Savona and Bruno, J. Nat. Prod., 46, 594, 1983, for Salvia willeana, de la Torre et al., Phytochemistry, 29, 668, 1990). It is also present in Salvia triloba and Salvia sclarea. Other possible terpenoids are shown below.

  According to some preferred embodiments, the composition comprises at least one diene-based compound (eg, isoprene, propadiene, and myrcene), and epoxides such as aromatic epoxides and fluorinated alkyl epoxides, DL- Hindered phenols such as α-tocopherol and 2-tert-butyl-4,6-dimethylphenol, diphenyl phosphate (eg Doverphos 213), and phosphines such as triphenyl phosphite alone and in mixtures such as Doverphos 9EII. It includes a combination of phytes, esters of phosphorous acid such as Doverphos 613, as well as one further stabilizing compound selected from the mixture of materials mentioned above.

  Any suitable relative amount of at least one diene-based compound and additional optional one or more stabilizer compounds can be used. For example, in some preferred embodiments, the weight ratio of one or more diene-based compounds to one or more other stabilizer compounds ranges from about 1:99 to about 100: 0. In more preferred embodiments, the weight ratio of the diene-based compound or compounds to optional stabilizer is from about 10: 1 to about 1: 1, more preferably from about 2: 1 to about 1: 1. Even more preferably, it is about 1: 1.

2. Phenols:
Any of a variety of phenolic compounds is contemplated as suitable for use as a stabilizer in the present composition. Although we do not wish to be bound by any theory of operation, we believe that the phenols tend to act as radical scavengers in the composition, thereby increasing the stability of such compositions. It is done. As used herein, the term “phenolic compound” generally refers to any substituted or unsubstituted phenol. Examples of suitable phenolic compounds include 4,4′-methylenebis (2,6-di-tert-butylphenol); 4,4′-bis (2,6-di-tert-butylphenol); 2,2- or 4,4-biphenyldiols such as 4,4′-bis (2-methyl-6-tert-butylphenol; derivatives of 2,2- or 4,4-biphenyldiols; 2,2′-methylenebis (4- Ethyl-6-tert-butylphenol); 2,2′-methylenebis (4-methyl-6-tert-butylphenol); 4,4-butylidenebis (3-methyl-6-tert-butylphenol): 4,4-isopropylidene Bis (2,6-di-tert-butylphenol); 2,2′-methylenebis (4-methyl-6-nonylphenol); Tylidenebis (4,6-dimethylphenol); 2,2'-methylenebis (4-methyl-6-cyclohexylphenol); 2,6-di-tert-butyl-4-methylphenol (BHT); 2,6-di -Tert-butyl-4-ethylphenol; 2,4-dimethyl-6-tert-butylphenol; 2,6-di-tert-α-dimethylamino-p-cresol; 2,6-di-tert-butyl-4 (N, N′-dimethylaminomethylphenol): 4,4′-thiobis (2-methyl-6-tert-butylphenol); 4,4′-thiobis (3-methyl-6-tert-butylphenol); 2′-thiobis (4-methyl-6-tert-butylphenol); bis (3-methyl-4-hydroxy-5-tert-butylbenzyl) And bis (3-5-di-tert-butyl-4-hydroxybenzyl) sulfide, etc. Other suitable phenols include tocopherol, hydroquinone; Some preferred phenols include tocopherol, BHT, hydroquinone, etc. Some particularly preferred phenols include tocopherol, etc. Most phenols are Irganox compounds from Ciba. A single phenolic compound and / or a mixture of two or more phenols can be used in the composition.

3. Epoxides:
It is also contemplated that any of a variety of epoxides are suitable for use in the compositions of the present invention. Of the epoxides, aromatic epoxides and fluorinated alkyl epoxides are preferred additional stabilizers in some embodiments. While the applicants do not wish to be bound by any theory of operation, the epoxides of the present invention act as acid scavengers in CF ₃ I compositions, thereby increasing the stability of such compositions. It is thought to have a tendency. Examples of suitable aromatic epoxides include the following formula I:

Wherein R is hydrogen, alkyl, fluoroalkyl, aryl, fluoroaryl, or

Is;
Ar is a substituted or unsubstituted phenylene or naphthylene group)
Are defined by Some preferred aromatic epoxides of Formula I include butylphenyl glycidyl ether; pentylphenyl glycidyl ether; hexylphenyl glycidyl ether; heptylphenyl glycidyl ether; octylphenyl glycidyl ether; nonylphenyl glycidyl ether; 1,4-diglycidylphenyl diether and derivatives thereof; 1,4-diglycidylnaphthyl diether and derivatives thereof; and 2,2 ′ [[[5-heptadecafluorooctyl] -1,3- Phenylene] bis [[2,2,2-trifluoromethyl] ethylidene] oxymethylene] bisoxirane and the like. Other preferred aromatic epoxides include naphthyl glycidyl ether, 4-methoxyphenyl glycidyl ether, and naphthyl glycidyl ether derivatives. Some more preferred aromatic epoxides include butylphenyl glycidyl ether and the like. A single aromatic epoxide and / or a mixture of two or more aromatic epoxides can be used in the composition.

  Any of a variety of alkyl and / or alkenyl epoxides are suitable for use in the present composition. Examples of suitable alkyl and alkenyl epoxides include those of formula II:

(Wherein R _alk is a substituted or unsubstituted alkyl or alkenyl group)
Can be mentioned. Preferably, R _alk is a substituted or unsubstituted alkyl or alkenyl group having about 1 to about 10 carbon atoms, more preferably about 1 to about 6 carbon atoms. Some preferred alkyl epoxides of Formula II include n-butyl glycidyl ether, isobutyl glycidyl ether, hexanediol diglycidyl ether, and the like, as well as fluorinated and perfluorinated alkyl epoxides. More preferred alkyl epoxides include hexanediol glycidyl ether and 1,2-epoxyhexane. Some preferred alkenyl epoxides of Formula II include allyl glycidyl ether, fluorinated and perfluorinated alkenyl epoxides, and the like. More preferred alkenyl epoxides include allyl glycidyl ether.

D. Other ingredients:
The composition can optionally include other ingredients depending on the particular intended use and the particular iodocarbon and stabilizing compound used.

1. Co-refrigerants, co-foaming agents, etc .:
According to some embodiments, as described more fully below, the composition of the present invention includes, depending on the intended use of the composition, in addition to the iodocarbon and stabilizer, if present. One or more components may be further included. For example, the composition can be generally adapted for use with the following applications, and these and other applications: heat transfer (including cooling, chiller applications, closed Rankine cycle operation (CRC)); organic Rankine cycle operation (ORC); foam and / or foam forming operation (premix and / or blowing agent and / or foam (such as polyurethane, polyisocyanurate, and phenolic resin) thermosetting foam (polystyrene and polyolefin) Such as thermoplastic foam, integral skin foam, including one-component or two-component pressurized floss foam) or as part thereof); solvent (including solvent washing and extraction); aerosol; oligomer And / or production of polymers (eg as monomers for polymerization reactions) A propellant; a fire extinguishing aid; a surfactant; a flushing application; a metered dose inhaler (MDI); a lubricant, a flame suppressant; a therapeutic composition; an insecticide composition; a herbicide composition; a solvent application (cleaning, extraction, And various other co-components can be used with the composition.

While it is contemplated that many co-components can be advantageously used in the present compositions, in some embodiments, the composition comprises the following components as co-components;
CO ₂ ;
Hydrocarbons (substituted and unsubstituted, especially hydrocarbons _C 2 _{~C 6);}
Alcohol (alcohol especially _C 2 -C ₆ substituted and unsubstituted)
Ketones (ketone in particular _C 2 -C ₅ substituted and unsubstituted);
Aldehyde (substituted and unsubstituted particular aldehyde _C 2 _{~C 5);}
Ether / diether (ether, especially _C 2 -C ₅ substituted and unsubstituted);
Fluoroether (especially fluoro ether _C 2 -C ₅ substituted and unsubstituted);
Fluoroalkenes (especially _C 2 -C ₆ fluoro alkene substituted and unsubstituted);
CFC (especially C ₂ -C ₅ CFC);
HFC (particularly HFC of _C 2 _{~C 5);}
HCC (particularly HCC of _C 2 _{~C 5);}
HCFC (particularly HCFC of _C 2 _{~C 5);}
Haloalkene, for example, preferably fluoro alkene (substituted and unsubstituted especially fluoro alkenes _C 2 _{~C 6);}
HFO (especially C ₂ -C ₅ HFO);
HClFO (especially HClFO of _C 2 _{~C 5);}
HBrFO (especially HBrFO of _C 2 _{~C 5);}
Carbonate / dicarbonate;
Carboxylic acids and derivatives thereof (eg carboxylic esters such as methyl formate); and water:
It is preferable to have one or more of the following.

  As used herein, the term “HFO” refers to a compound composed of carbon, fluorine, and hydrogen atoms, free of other atoms and having at least one carbon-carbon double bond.

  As used herein, the term “HClFO” refers to a compound composed of carbon, chlorine, fluorine and hydrogen atoms, free of other atoms and having at least one carbon-carbon double bond.

  As used herein, the term “HBrFO” refers to a compound composed of carbon, bromine, fluorine, and hydrogen atoms, free of other atoms and having at least one carbon-carbon double bond.

The use of symbols C ₁ -C _5, etc. as used throughout the specification and claims refers to compounds having at least one carbon atom and up to about 5 carbon atoms.
Although it is contemplated that a wide range of HFCs can be used in the present compositions and methods, in some preferred embodiments, the following components (including all isomers of each):
Difluoromethane (HFC-32);
Pentafluoroethane (HFC-125);
1,1,2,2-tetrafluoroethane (HFC-134);
1,1,1,2-tetrafluoroethane (HFC-134a):
Trifluoroethane (HFC-143a);
Difluoroethane (HFC-152a);
1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea):
1,1,1,3,3,3-hexafluoropropane (HFC-236fa)
1,1,1,3,3-pentafluoropropane (HFC-245fa); and 1,1,1,3,3-pentafluorobutane (HFC-365mfc);
It is preferable to use one or more of these in the composition.

  Although it is contemplated that a wide range of HCFCs can be used in the present compositions and methods, in some preferred embodiments, dichlorotrifluoroethanes (eg, 2,2-dichloro-1,1,1-trifluoroethane) (HCFC-123)); and chlorotetrafluoroethane (HCFC-124); (including all isomers of each) are preferably used separately or in any combination.

  Although it is contemplated that a wide range of HCCs can be used in the present compositions and methods, in some preferred embodiments, dichloroethanes (eg, 1,2-dichloroethane such as trans-1,2-dichloroethane); Preferably, ethyl; and 2-chloropropane; are used separately or in any combination.

  Although it is contemplated that a wide range of CFCs can be used in the present compositions and methods, in preferred embodiments, trichlorotrifluoroethanes (eg, 1,1,2-trichlorotrifluoroethane (CFC-113)) are used, It is particularly preferred to use it as a monomer for producing oligomers and / or polymers.

While it is contemplated that a wide range of fluoroalkenes can be used in the present compositions and methods, in many embodiments, the composition comprises one or more C ₃ or C ₄ fluoroalkenes, preferably I:
XCF _z R _3-z (I)
Wherein X is a C ₂ or C ₃ unsaturated, substituted or unsubstituted alkyl group, each R is independently Cl, F, Br, I, or H, and z is 1 ~ 3)
It is particularly preferred to include a compound having Among the compounds of formula I, the following compounds:
Fluoroethenes;
Fluoropropenes;
Fluorobutenes;
Chlorofluoroethenes;
Chlorofluoropropenes; and chlorofluorobutenes;
Is highly preferred.

Among the fluoroethenes, C ₂ H ₃ F (monofluoroethylene or vinyl fluoride or VF); C ₂ H ₂ F ₂ (eg 1,1-difluoroethylene (vinylidene fluoride or VDF)); C ₂ HF ₃ (trifluoroethylene or THFE); and C ₂ F ₄ (tetrafluoroethylene or TFE); are preferred for use in some embodiments of the present invention.

Among the fluoropropenes, C ₃ H ₃ F ₃ (including all isomers such as 3,3,3-trifluoropropene (HFO-1243zf)); C ₃ H ₂ F ₄ (eg 1,3 , 3,3-tetrafluoropropene (HFO-1234ze) and 2,3,3,3-tetrafluoropropene (HFO-1234yf) cis and trans isomers); and C ₃ HF ₅ (eg, isomers of HFO-1225) Are preferred for use in some embodiments of the present invention.

  The term “HFO-1234” is used herein to refer to all tetrafluoropropenes. Tetrafluoropropenes include HFO-1234yf and all stereo or geometric isomers thereof. The terms “HFO-1234yf” and “HFO-1234ze” are used herein to refer to 1,1,1,2-tetrafluoropropene and 1,1,1,3-tetra, respectively, regardless of their stereoisomerism. Fluoropropene is used to refer generically.

The compound of HFO-1234 is a known substance and is shown in the Chemical Abstracts database. The preparation of fluoropropenes such as CF ₃ CH═CH ₂ by catalytic vapor phase fluorination of various saturated and unsaturated halogen-containing C ₃ compounds is described in US Pat. Nos. 2,889,379; 4,798,818; 4,465,786, each of which is incorporated herein by reference. In EP-974,571 (also incorporated herein by reference), 1,1,1,3,3-pentafluoropropane (HFC-245fa) is added to chromium at elevated temperature in the vapor phase. The 1,1,1,3-tetrafluoropropene can be contacted with a base catalyst or with an alcohol solution of KOH, NaOH, Ca (OH) ₂ or Mg (OH) _{2 in} the liquid phase. Manufacturing is disclosed.

Among the fluorobutenes, C ₄ H ₄ F ₄ (including all isomers thereof); C ₄ H ₃ F ₅ (eg, all isomers of HFO-1345); and C ₄ H ₂ F ₆ (eg, All isomers of HFO-1336) are preferred for use in some embodiments of the present invention.

Of the chlorofluoroethenes, C ₂ F ₃ Cl (CTFE) is preferred for use in some embodiments of the present invention.
Among the chlorofluoropropenes, for example, C ₃ H ₂ F ₄ Cl (for example, 2-chloro-3,3,3-trifluoro-1-propene (including HCFO-1233xf), and 1-chloro-3, Mono- or dichlorinated compounds such as 3,3-trifluoro-1-propene (including all isomers of HCFO-1233zd) are preferred for use in some embodiments of the present invention.

  In some preferred embodiments of the invention, the composition has the following formula II:

Wherein each R is independently Cl, F, Br, I, or H;
R ′ is (CR ₂ ) _n Y;
Y is CRF ₂ ; and n is 0 or 1)
At least one fluoroalkene.

In a highly preferred embodiment, Y is CF ₃ , n is 0 and at least one of the remaining R is F.
Applicants have generally found that the compounds of formulas I and II defined above, when included in the composition, all of the uses defined above (particularly the refrigerant compositions, blowing agent compositions of the present invention). It is generally effective in compatibilizers, aerosols, propellants, fragrances, flavor formulations, solvent compositions, etc.) and is considered useful. However, Applicants have surprisingly and unexpectedly found that some compounds having a structure according to the formula described above are highly desirable at low levels of toxicity compared to other such compounds. It was found to show. As will be readily appreciated, this discovery is very advantageous and beneficial not only for the formulation of refrigerant compositions, but also for the formulation of all compositions containing relatively toxic compounds that satisfy the above described formula. There is a possibility. More specifically, Applicants have found that relatively low levels of toxicity are preferably that Y is CF ₃ , at least one R on the unsaturated terminal carbon is H, and at least one of the remaining R is F. Considered to be associated with certain compounds of formula II. Applicants also consider that all structural isomers, geometric isomers, and stereoisomers of such compounds are effective and beneficially of low toxicity.

  In highly preferred embodiments, particularly those comprising the above low toxicity compounds, n is 0. In some highly preferred embodiments, the compositions of the present invention comprise one or more tetrafluoropropenes. The term “HFO-1234” is used herein to refer to all tetrafluoropropenes. Of the tetrafluoropropenes, HFO-1234yf is highly preferred for use with heat transfer compositions, methods, and systems.

  In other embodiments, it may be preferred to use either or both of cis- and trans-1,3,3,3-tetrafluoropropene (HFO-1234ze). The term HFO-1234ze is used herein to refer generically to 1,3,3,3-tetrafluoropropene, regardless of whether it is in the cis or trans form. The terms “cis-HFO-1234ze” and “trans-HFO-1234ze” are used herein to indicate the cis and trans forms of 1,3,3,3-tetrafluoropropene, respectively. Accordingly, the term “HFO-1234ze” includes within its scope cis-HFO-1234ze, trans-HFO-1234ze, and all combinations and mixtures thereof.

  Although the properties of cis-HFO-1234ze and trans-HFO-1234ze differ in at least some respects, each of these compounds can be used alone or with respect to each of the applications, methods, and systems described herein. It is contemplated that it can be adapted for use with other compounds including the stereoisomers. For example, trans-HFO-1234ze may be suitable for use in some cooling systems because of its relatively low boiling point (−19 ° C.), however, a cis having a boiling point of + 9 ° C. -HFO-1234ze is also believed to have utility in some cooling systems of the present invention. Thus, the terms “HFO-1234ze” and 1,3,3,3-tetrafluoropropene should be understood to refer to both stereoisomers, and the use of such terms, unless otherwise indicated. Each of the cis and trans forms is intended to be applied and / or intended to be useful for the indicated purpose.

The compound of HFO-1234 is a known material and is shown in the Chemical Abstracts database. Preparation of fluoropropenes such as CF ₃ CH═CH ₂ by catalytic vapor phase fluorination of various saturated and unsaturated halogen containing C ₃ compounds is described in US Pat. Nos. 2,889,379; 4,798,818; , 465, 786; each of which is incorporated herein by reference. In EP-974,571 (also incorporated herein by reference), 1,1,1,3,3-pentafluoropropane (HFC-245fa) is chromium-based at elevated temperature in the vapor phase. Of 1,1,1,3-tetrafluoropropene by contacting with an alcohol catalyst of KOH, NaOH, Ca (OH) ₂ or Mg (OH) _{2 in} the liquid phase Is disclosed. In addition, the process for preparing the compounds according to the invention is described, by way of non-limiting example, in pending US patent application 10 / 694,272 “Process for the preparation of fluoropropenes” and US provisional application 60/733355 (2005). Filed on Nov. 3), each of which is incorporated herein by reference.

  The present compositions, particularly those comprising HFO-1234 and HFO-1234yf, are believed to have several properties that are advantageous for a number of important reasons. For example, Applicants have found that, based at least in part on a mathematical model, the fluoroolefins of the present invention have no substantial adverse impact on environmental chemistry, and some other halogenated species and Compared to the ozone layer destruction, it is considered to be a negligible substance. Thus, preferred compositions of the present invention have the advantage of not substantially contributing to ozone layer destruction. Preferred compositions also do not substantially contribute to global warming compared to many of the currently used hydrofluoroalkanes.

  The amount of the compound of formula I, particularly HFO-1234, contained in the composition can vary widely depending on the particular application, and compositions comprising more than about 1% by weight and less than 100% of the compound of the present invention Is within a wide range. In a preferred embodiment, the composition comprises HFO-1234, preferably HFO-1234yf, in an amount of about 5% to about 99%, even more preferably about 5% to about 95%.

  By way of example (but not necessarily for purposes of limitation), some preferred embodiments of the present compositions include the present compounds in addition to (and in addition to stabilizer compounds, if present) the present iodocarbon compounds. Inventive fluoroalkene compounds and / or HFCs are broad compositional ranges, intermediate compositional ranges and more specific compositional ranges shown in the table below (all amounts are understood to be preceded by “about”) (Where the percentages are based on the total weight of the three components shown in Table 1 below).

Some preferred embodiments of the present composition include CF ₃ I and one type in addition to the stabilizer that is preferably present in the heat transfer fluid according to the present invention and any oil or lubricant that is also preferably present. The above fluoroalkene compounds can be included. In some preferred forms, the fluoroalkene consists essentially of tetrafluoropropene, more preferably HFO-1234yf. A broad composition range, an intermediate composition range, and a more specific composition range (all amounts are understood to be preceded by “about”) are shown in the table below, where the percentages are shown in Table 2 below. It is based on the sum of the components that are generated.

Some highly preferred embodiments of the present invention include from about 65 to about 75% by weight HFO-1234yf and from about 25 to about 35% by weight CF ₃ I, even more preferably from about 70% by weight HFO-1234yf and about Including heat transfer fluids, particularly for use in automotive air conditioning systems, including 30 wt% CF ₃ I (such percentages are based on the combined weight of HFO and CF ₃ I).

Some highly preferred embodiments of the composition include, in addition to any stabilizer present in accordance with the invention, CF ₃ I, some fluoroalkene compounds of the invention (preferably HFO-1234ze), and And / or several HFCs (preferably HFC-152a) with a broad composition range, an intermediate composition range, and a more specific composition range as shown in the table below (all amounts are preceded by “about”) Understood) (where percentages are based on the sum of the three components shown in Table 3).

Some preferred embodiments of the composition include CF ₃ I, some fluoroalkene compounds of the invention, and / or some HFCs (preferably HFC-32) in addition to the stabilizers of the invention. , Broad composition ranges shown in the table below, intermediate composition ranges, and more specific composition ranges (all amounts are understood to be prefixed with “about”) (where percentages are shown in Table 4) Based on the sum of the two components).

2. lubricant:
According to some forms of the invention, the composition comprises a lubricant or oil in addition to one or more iodocarbon compounds. Any of a variety of conventional lubricants can be used in the compositions of the present invention. Such compositions are particularly well suited for use as refrigerants in heating or cooling cycle devices, as described more fully below. The composition then includes at least one lubricant having hydrogen atoms and carbon atoms, wherein 17% or less of the total number of hydrogen atoms bonded to the carbon atoms is a tertiary hydrogen atom. Preferably, the lubricant is less than 1% of the total number of hydrogen atoms bonded to carbon atoms is tertiary hydrogen atoms, more preferably has no tertiary hydrogen atoms, ie in this case, About 0% of the total number of hydrogen atoms bonded to carbon atoms is tertiary hydrogen atoms.

  It also preferably has a relatively low proportion of oxygen in the molecule and preferably no oxygen in the molecule. It is also generally preferred to use a polar solvent with a slight natural concentration, especially a lubricant or oil having only water. An important requirement for the lubricant is that enough lubricant must be returned to the system compressor in order for the compressor to be lubricated. Thus, lubricant stability is determined in part by refrigerant / lubricant characteristics and in part by system characteristics. Examples of suitable lubricants include mineral oils, alkylbenzenes, such as synthetic lubricants, specifically polyalkylene glycol (PAG) lubricants, preferably consisting essentially of two or more oxypropylene groups, about 37 PAGs having a viscosity of about 10 to about 200 centistokes at ℃ (sold under the trade name ND-8 by Idemitsu Kosan), and PAGs sold under the trade name RL-897 by DOW, polyvinyl ethers (PVE). Preferred lubricants include naphthenic mineral oils, paraffinic mineral oils, ester oils, polyalkylene glycols, polyvinyl ethers, alkylbenzenes, poly α-olefins, polyesters, polyol esters, or combinations thereof. Mineral oils including paraffinic or naphthenic oils are commercially available. Commercially available mineral oils include Witco LP250® from Witco, Zerol 300® from Shrieve Chemical, Sunisco 3GS from Witco, and Calumet R015 from Calumet. Commercially available alkyl benzene lubricants include Zerol 150®. Commercially available esters include neopentyl glycol dipelargonate available as Emery 2917® and Hatcol 2370®. Other useful esters include phosphate esters, dibasic acid esters, and fluoroesters. In some cases, hydrocarbon-based oils are sufficiently soluble with refrigerants containing iodocarbon, and the combination of iodocarbon and hydrocarbon oil is more stable than other types of lubricants. there is a possibility. Such a combination may therefore be advantageous. Polyalkylene glycols are highly preferred in some embodiments because they are currently used in certain applications such as mobile air conditioning. Mixtures of different lubricants can be used.

  One aspect of the present invention includes selecting a lubricant comprising a major proportion by weight of alkylbenzene-based compound, mineral oil compound, and combinations thereof, and even more preferably at least about 75% by weight. With respect to alkylbenzenes, Applicants have found that such compounds have a relatively high level of miscibility in preferred refrigerant compositions, and the relatively high levels that such molecules exhibit in the heat transfer compositions and heat transfer systems of the present invention. It has been found that it is preferred among a number of lubricant compounds available so far for stability. Other molecules preferred for use in connection with the present invention are referred to in the present invention as ethylene oxide / propylene oxide (EO / PO) molecules for convenience (but not for purposes of limitation). Such a molecule has the structure shown below in a preferred embodiment.

  Applicants have identified such EO / PO molecules (in the present invention, the presence of a methyl group or other relatively short chain length alkyl group on each end of the molecule, resulting in a “double cap EO / It has been found that "also called" PO molecules ") can provide the ability to adjust the values of n and m \ to suit each particular application. Thus, the lubricant molecules can be selected to achieve a very advantageous combination of miscibility and stability. The advantages afforded by double-capped molecules are substantially better in many respects than similar molecules that are capped only at one end, as shown in the examples below. US Pat. No. 4,975,212 (incorporated herein by reference) discloses a technique for capping this type of molecule. Although generally not preferred, the preferred lubricants of the present invention can be combined with one or more conventional lubricants.

  Suitable polyol ester lubricants suitable for air conditioning or cooling applications are usually pure or mixed with polyalcohol or polyol compounds such as pentaerythritol, dipentaerythritol, neopentyl glycol, or trimethylpropanol. Prepared by condensation with a linear or branched aliphatic carboxylic acid, such as a linear or branched monocarboxylic acid having from about 4 to about 10 carbon atoms. Polyol ester base stock polyols are available from Hatco Corporation. For example, Hatcol 3307 is a pure polyol ester base stock based on neopentyl glycol. Hatcol 3329 and Hatcol 3504 are pure polyol ester cooled base stocks based on pentaerythritol mixed fatty acid esters. Hatcol 3316 is a polyol ester of dipentaerythritol and short chain fatty acids. Other examples of such polyol ester lubricant formulations include polyol ester cooling lubricants from the Cognis ProEco® line, polyol esters from ICI's EMKARATE RL line, and subsidiaries of CPI Engineering Services, Inc. such as Solest. Polyol ester lubricants provided by Lubrizol. Preferred compositions according to the present invention comprise a lubricant in an amount of from about 20% to about 50%, preferably from about 20% to about 30% by weight of the composition.

3. Other ingredients:
Any of a variety of other additives can be used in the compositions of the present invention. Examples of suitable additives include metal passivators such as nitromethane, extreme pressure (EP) additives that improve the lubricity and load bearing properties of the lubricant. Examples of EP additives are described in US Pat. No. 4,755,316 (Table D), which is included herein. Examples of EP additives are organic phosphates such as Lubrizol® 8478 manufactured by Lubrizol Corporation. Corrosion inhibitors are also effective and are disclosed in 4,755,316 (Table D).

II. Heat transfer composition:
While it is contemplated that the compositions of the present invention can include a wide range of amounts of each of the compounds referred to herein, the heat transfer composition, particularly the refrigerant composition of the present invention, can be a plurality of iodocarbon compound, even more preferably iodo fluorocarbon compounds of C ₁ -C _3, it is generally preferred to include an amount of at least about 25% by weight of the composition. In some preferred embodiments where the composition comprises HFC, particularly HFC-152a, the composition comprises at least about 40% by weight, and even more preferably at least about 50% by weight HFC-152a.

  Preferred refrigerants or heat transfer compositions according to the present invention, particularly those used in vapor compression systems, contain a lubricant, generally in an amount of about 30 to about 50% by weight of the composition. An important requirement for the lubricant is that enough lubricant must be returned to the system compressor to lubricate the compressor. Thus, the suitability of a lubricant is determined in part by refrigerant / lubricant characteristics and in part by system characteristics. Examples of suitable lubricants include mineral oil, alkylbenzenes, polyol esters (including polyalkylene glycols), polyvinyl ethers (PVE), and the like. Mineral oils including paraffinic or naphthenic oils are commercially available. Commercially available mineral oils include Witco LP250® from Witco, Zerol 300® from Shrieve Chemical, Sunisco 3GS from Witco, and Calumet R015 from Calumet. Commercially available alkyl benzene lubricants include Zerol 150®. Commercially available esters include neopentyl glycol dipelargonate available as Emery 2917® and Hatcol 2370®. Other useful esters include phosphate esters, dibasic acid esters, and fluoroesters. In some cases, hydrocarbon-based oils are sufficiently soluble with refrigerants containing iodocarbon, and the combination of iodocarbon and hydrocarbon oil may be more stable than other types of lubricants. is there. Thus, such a combination may be advantageous. Preferred lubricants include polyalkylene glycols and esters. Polyalkylene glycols are highly preferred in some embodiments because they are currently used in certain applications such as mobile air conditioning. Of course, different mixtures of different types of lubricants can be used.

  The preferred form of the composition may also contain a compatibilizer such as propane for the purpose of promoting the compatibility and / or solubility of the lubricant. Such compatibilization such as propane, butanes, and pentanes is preferably present in an amount of about 0.5 to about 5% by weight of the composition. Also, as disclosed by US Pat. No. 6,516,837 (the disclosure of which is incorporated herein by reference), a combination of surfactant and solubilizer is used to enhance oil solubility. It can also be added to the composition.

  Many existing cooling systems are currently suitable for use with existing refrigerants, and some compositions of the present invention may be used in many such systems with or without modification of the system. It is thought that it can be adapted. In many applications, the compositions of the present invention can provide an alternative advantage in refrigerant-based systems that currently have relatively high capacity. Further, in embodiments where it is desirable to replace a higher capacity refrigerant with a lower capacity refrigerant composition of the present invention, eg, for cost reasons, such an embodiment of the composition provides a potential advantage. Thus, in some embodiments, the composition of the present invention includes a substantial proportion of trans-HFO-1234yf as an alternative to existing refrigerants, particularly HFC-134a, and in some embodiments a major It is preferred to use a composition containing a proportion of trans-HFO-1234yf. In some applications, the refrigerants of the present invention potentially enable the beneficial use of larger positive displacement compressors, resulting in better energy efficiency than other refrigerants such as HFC-134a. It is done. Thus, the refrigerant compositions of the present invention, particularly those comprising trans-HFP-1234ze, offer the potential to gain an energy-based competitive advantage for refrigerant replacement applications.

The compositions of the present invention, particularly those comprising HFO-1234 (especially HFO-1234yf), are also advantageous (in the original system or in R-12 and R-500) in chillers commonly used for commercial air conditioning systems. Or any one of the alternatives to the refrigerant. In some such embodiments, from about 0.5 to about 60%, more preferably from about 20 to about 50% by weight of a flammability inhibitor, preferably CF ₃ I according to the present invention, in the HFO-1234 composition. It is preferable to contain iodocarbon such as

Thus, the methods, systems, and compositions are used in connection with automotive air conditioning systems and equipment, commercial cooling systems and equipment, chillers , residential refrigerators and freezers, general air conditioning systems, heat pumps, ORC, CRC, and the like. Can be adapted.

III. Foaming agent, foam, and foamable composition:
The blowing agent can also comprise or consist of one or more of the present compositions. As noted above, the compositions of the present invention can include a wide range of amounts of one or more iodocarbon compounds and one or more diene-based compounds of the present invention. However, with respect to preferred compositions for use as blowing agents according to the present invention, the one or more iodocarbon compounds are present in an amount of at least about 1%, even more preferably at least about 50% by weight of the composition. Is generally preferred.

In some preferred embodiments, the blowing agent composition of the present invention comprises the following ingredients in addition to HFO-1234 (preferably HFO-1234ze):
Difluoromethane (HFC-32);
Pentafluoroethane (HFC-125);
1,1,2,2-tetrafluoroethane (HFC-134);
1,1,1,2-tetrafluoroethane (HFC-134a);
Difluoroethane (HFC-152a);
1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea);
1,1,1,3,3,3-hexafluoropropane (HFC-236fa);
1,1,1,3,3-pentafluoropropane (HFC-245fa);
1,1,1,3,3-pentafluorobutane (HFC-365mfc);
water;
CO ₂ ;
Methyl formate and its derivatives;
Alcohols (C ₁ -C ₄ ) and derivatives thereof;
Ketones and derivatives thereof;
Aldehydes and derivatives thereof;
Ethers / diethers and derivatives thereof;
Carbonates and derivatives thereof;
Dicarbonates and derivatives thereof; and carboxylic acids and derivatives thereof:
One or more of these as co-blowing agents, fillers, vapor pressure regulators, or for any other purpose.

  It is contemplated that the blowing agent composition of the present invention can include cis-HFO-1234ze, trans-HFO-1234ze, or combinations thereof. In some preferred embodiments, the blowing agent composition of the present invention comprises a combination of cis-HFO-1234ze and trans-HFO-1234ze from about 1:99 to about 30:70, even more preferably about 1:99. In a cis: trans weight ratio of about 5:95.

  In other embodiments, the present invention provides a foamable composition, preferably polyurethane, polyisocyanurate, phenolic foam, extruded thermoplastic foam composition, integral skin foam, made using the composition of the present invention, And a one-component or two-component pressurized floss foam. In such foam embodiments, one or more of the present compositions are preferably reacted with and / or foamed under conditions suitable to form a foam or cellular structure as is well known in the art. In the foamable composition containing the component which becomes, it is included as a foaming agent or its part. The present invention also relates to a foam, preferably a closed cell foam, made from a polymer foam formulation that includes a blowing agent comprising the composition of the present invention. In yet another aspect, the present invention relates to a foamable composition comprising thermoplastic foam such as polystyrene (PS), polyethylene (PE), polypropylene (PP), and polyethylene terephthalate (PET) foam, preferably low density foam. Offer things.

  In some preferred embodiments, dispersants, foam stabilizers, surfactants, and other additives may be included in the blowing agent composition of the present invention. A surfactant is optionally, however, preferably added to act as a foam stabilizer. Some exemplary materials are disclosed in US Pat. Nos. 2,834,748; 2,917,480; and 2,846,458; each of which is incorporated herein by reference. Such as the ones sold under the names DC-193, B-8404, and L-5340, which are generally polysiloxane polyoxyalkylene block copolymers. Other optional additives for the blowing agent mixture include tri (2-chloroethyl) phosphate, tri (2-chloropropyl) phosphate, tri (2,3-dibromopropyl) phosphate, tri (1,3- Flame retardants such as dichloropropyl) phosphate, diammonium phosphate, various halogenated aromatic compounds, antimony oxide, aluminum trihydrate, polyvinyl chloride and the like.

IV. Propellant composition:
In another form, the present invention provides a propellant composition comprising or consisting essentially of the composition of the present invention, such propellant composition is preferably a sprayable composition. The propellant composition of the present invention preferably comprises a propellant which comprises, consists essentially of or consists of the substance to be sprayed and the composition according to the invention. Inert ingredients, solvents, and other materials can also be present in the sprayable mixture. Preferably, the sprayable composition is an aerosol. Suitable substances to be sprayed include, without limitation, cosmetic substances such as deodorants, perfumes, hair sprays, facial creams, and polishes, as well as anti-asthma and halitosis drugs, and preferably inhaled. Or any other medicament or drug substance, such as any other medicament intended. The medicament or other therapeutic agent is preferably present in the composition in a therapeutic amount, and the remaining substantial proportion of the composition is comprised of a compound of formula I of the present invention, preferably HFO-1234, and even more preferably HFO-1234ze. including.

  Aerosol products for industrial, consumer, or medical applications typically contain one or more propellants along with one or more active ingredients, inert ingredients, or solvents. The propellant provides a force for discharging the product in an aerosolized form. Some aerosol products inject using compressed gases such as carbon dioxide, nitrogen, nitrous oxide, and even air, but most commercial aerosols use liquefied gas propellants. The most commonly used liquefied gas propellants are hydrocarbons such as butane, isobutane, and propane. Dimethyl ether and HFC-152a (1,1-difluoroethane) are also used alone or in blends with hydrocarbon propellants. Unfortunately, all of these liquefied gas propellants are highly flammable, and when they are introduced into an aerosol formulation, often flammable aerosol products are obtained.

  Applicants have come to recognize the continuing need for non-flammable liquefied gas propellants using them to formulate aerosol products. The present invention relates to several industrial aerosol products including, for example, spray detergents, lubricants, and the like, and pharmaceutical aerosols for use in, for example, pharmaceutical aerosols for delivering drugs to the lungs or mucous membranes. Compositions, in particular and preferably HFO-1234, even more preferably compositions comprising HFO-1234ze and / or HFO-1234yf are provided. Examples of this include metered dose inhalers (MDIs) for the treatment of asthma and other chronic obstructive pulmonary diseases and for delivering drugs into the accessible mucosa or nasal cavity. Thus, the present invention includes the application of a composition of the present invention comprising a drug or other therapeutic ingredient to an organism in need of treatment, an organism disease (such as a human being or animal), a disease, and the like. Includes methods for treating health related problems. In some preferred embodiments, the step of applying the composition provides an MDI comprising the composition of the invention (eg, introducing the composition into the MDI) and then releasing the composition from the MDI. Including that.

  The composition of the present invention, particularly a composition comprising or comprising a major proportion of HFO-1234 (preferably HFO-1234ze and / or HFO-1234yf), is a non-flammable liquefied gas that does not substantially contribute to global warming. Propellants and aerosols can be provided. The composition includes various industrial aerosols or other sprayable compositions such as contact cleaners, dusters, lubricant sprays, etc., as well as consumer aerosols such as personal care products, household products, and automotive products. Can be used to blend. HFO-1234ze is particularly preferred for use as an important component of propellant compositions in pharmaceutical aerosols such as metered dose inhalers. The pharmaceutical aerosols and / or propellants and / or sprayable compositions of the present invention in many applications are in addition to compounds of formula (I) or (II) (preferably HFO-1234ze), beta agonists, Includes corticosteroids, or other drugs, and optionally other ingredients such as surfactants, solvents, other propellants, flavors, and other excipients. The compositions of the present invention, unlike many compositions used so far in these applications, have good environmental properties and are not likely to contribute to global warming. The composition thus provides, in some preferred embodiments, a substantially non-flammable liquefied gas propellant having a very low global warming potential.

V. Flavoring and flavoring:
The compositions of the present invention also provide advantages when used as part of flavor and fragrance formulations, particularly as carriers for them. The suitability of this composition for this purpose is demonstrated by a test procedure in which 0.39 g of jasmon is placed in a thick glass tube. 1.73 g of R-1234ze was added to the glass tube. The tube was then frozen and sealed. When the tube was thawed, the mixture was found to have one liquid phase. This solution contains 20% by weight jasmon and 80% by weight R-1234ze, thus its preferred use as part of a carrier or delivery system for flavor formulations in aerosols and other formulations. Was established. In addition, its potential as an extractant for fragrances from plants and the like is also probable. In some embodiments, it may be preferred to use the composition in extraction applications using the supercritical fluid. This and other applications involving using the present compositions in supercritical or near supercritical state are described below.

VI. Stabilizer composition:
The present invention, in one form, as any additive in any one of the above compositions, or more generally any composition comprising or exposed to one or more iodocarbon compounds. A stabilizer composition for use as an additive for is provided. Accordingly, in such a composition, there is no need for the presence of one or more iodocarbon compounds, but the presence of the diene-based compound described above. In a preferred embodiment, the stabilizer composition of the present invention is selected from the group of one or more diene-based compounds, as well as the further stabilizers described above, preferably one or more phenolic compounds, one type Or a combination of at least one additional stabilizer selected from the group consisting of a plurality of epoxy compounds, phosphites, phosphates, and combinations thereof.

VI. Methods and systems:
The compositions of the present invention are useful with a number of methods and systems, such as heat transfer fluids in methods and systems for transferring heat, such as refrigerants used in cooling, air conditioning, and heat pump systems. The composition is also advantageous for use in systems and methods for producing aerosols that preferably comprise or consist of an aerosol propellant in such systems and methods. Methods for forming foam and methods for extinguishing and extinguishing are also included in some forms of the invention. The present invention also provides, in some forms, a method for removing residues from articles using the composition as a solvent composition in such methods and systems.

A. Heat transfer method:
Preferred heat transfer methods generally involve providing a composition of the invention and transferring heat to or from the composition by changing the phase of the composition and / or by sensible heat transfer. For example, the method preferably provides cooling by absorbing heat from a fluid or article by evaporating the refrigerant composition in the vicinity of the object or fluid to be cooled to produce a vapor containing the composition. Preferably, the method includes the further step of compressing the refrigerant vapor, usually by a compressor or similar device, to produce a relatively high pressure vapor of the composition. In general, the process of compressing the steam adds heat to the steam, which causes an increase in the temperature of the relatively high pressure steam. Preferably, the method includes removing at least a portion of the heat applied by the evaporation and compression steps from the relatively hot and high pressure steam. The heat removal step preferably includes condensing the high pressure and high pressure vapor while the vapor is in a relatively high pressure condition to produce a relatively high pressure liquid comprising the composition of the present invention. The relatively high pressure liquid is then preferably subjected to an apparent enthalpy depressurization to produce a relatively low temperature and low pressure liquid. In such an embodiment, this reduced temperature refrigerant liquid is evaporated by heat transferred from the next object or fluid to be cooled.

  In another method aspect of the present invention, the composition of the present invention can be used in a method of generating heating that includes condensing a refrigerant containing the composition in the vicinity of the liquid or object to be heated. As described above, such a method is often a cycle opposite to the above cooling cycle.

B. Foam foaming method:
One aspect of the invention relates to a method of forming foam, preferably polyurethane and polyisocyanurate foam. This method generally provides a blowing agent composition of the invention, adds the blowing agent composition (directly or indirectly) to the foamable composition, and forms a foam or cellular structure, as is well known in the art. Reacting the foamable composition under conditions effective for this. Such techniques such as those described in "Polyurethanes Chemistry and Technology", Volumes I and II, Saunders and Frisch, 1962, John Wiley and Sons, New York, NY, which is hereby incorporated by reference. Any method known in can be used or adapted to be used in accordance with the foam aspect of the present invention. In general, such preferred methods include isocyanates, polyols or mixtures of polyols, blowing agents comprising one or more of the present compositions or mixtures of blowing agents, and catalysts, surfactants, and in some cases difficult. Including the formation of polyurethane or polyisocyanurate foams by blending other materials such as flame retardants, colorants, or other additives.

  It is advantageous in many applications to provide the ingredients for the polyurethane or polyisocyanurate foam in a pre-blended formulation. Most commonly, the foam formulation is pre-blended into two components. The isocyanate and optionally some surfactants and blowing agents constitute the first component, commonly referred to as the “A” component. The polyol or polyol mixture, surfactant, catalyst, blowing agent, flame retardant, and other isocyanate-reactive components constitute a second component, commonly referred to as the “B” component. Thus, the components on the A and B sides are mixed by hand for small preparations and preferably form blocks, slabs, laminates, in-situ injection panels, and other articles, spray application foam, floss, etc. Polyurethane or polyisocyanurate foams are easily produced by mixing by mechanical mixing techniques. In some cases, other ingredients such as flame retardants, colorants, blowing agents, and even other polyols can be added to the mixing head or reaction site as a third stream. Also, in some cases, each of these components can be added in part to the B component and in part as a third stream to the mixing head or reaction site. Most preferably, however, they are all introduced into the one B component described above.

  A thermoplastic foam can also be produced using the composition of the present invention. For example, conventional polystyrene and polyethylene blends can be mixed with the composition in a conventional manner to produce a rigid foam.

C. Cleaning method:
The present invention also provides a method of removing contaminants from a product, member, part, substrate, or any other article or part thereof by applying the composition of the invention to the article. For convenience purposes, the term “article” is used herein to refer to all such products, components, parts, substrates, etc., or even any surface or portion thereof. Is intended to be. Furthermore, the term “contaminant” is intended to refer to any undesirable material or substance present on an article, even if the substance is intentionally placed on the article. . For example, in the manufacture of semiconductor devices, it is common to deposit a photoresist material on a substrate to form a mask for an etching process, and then remove the photoresist material from the substrate. As used herein, the term “contaminant” is intended to cover and encompass such photoresist materials.

A preferred method of the invention involves applying the composition to an article. Although it is contemplated that the composition of the present invention can be successfully used in many different cleaning methods, it is believed that the composition is particularly advantageous for use with supercritical cleaning methods. Supercritical cleaning is disclosed in US Pat. No. 6,589,355, assigned to the assignee of the present invention and incorporated herein by reference. For supercritical cleaning applications, in some embodiments, in addition to HFO-1234 (preferably HFO-1234ze), as well as CO ₂ and other additional components known for use with supercritical cleaning applications. Preferably, one or more additional ingredients are included in the cleaning composition. Also, in some embodiments, the cleaning composition may be and may be desirable for certain vapor degreasing and solvent cleaning methods, including some applications, particularly complex parts, to remove dirt. For those that are difficult to do, steam degreasing and solvent cleaning methods are particularly preferred. A preferred vapor degreasing and solvent washing process consists of exposing the article to solvent vapor, which is preferably boiling at room temperature. Condensing the vapor over the object has the advantage of providing a relatively clean distilled solvent to wash away oils or other contaminants. Thus, such a process has the further advantage that relatively little residue remains by finally evaporating the solvent composition from the object as compared to simply washing the object in a liquid solvent. Have sex.

  For applications where the article contains contaminants that are difficult to remove, the present invention substantially increases the temperature of the solvent composition of the present invention above ambient temperature or the cleaning action of the solvent in such applications. It is preferred to include raising to any other temperature effective to do so. Such a process is also generally preferred for operation of large assembly lines where cleaning of articles, particularly metal parts and assemblies, must be done efficiently and quickly.

  In a preferred embodiment, the cleaning method of the present invention comprises immersing the article to be cleaned in a liquid solvent at an elevated temperature, even more preferably at about the boiling point of the solvent. In such operations, this step preferably removes a substantial amount, and even more preferably, the majority of the target contaminant from the article. Following this step, the article is preferably immersed in a solvent below the temperature of the liquid solvent in the previous immersion step, preferably at about ambient or room temperature, preferably freshly distilled solvent. The preferred method also then contacts the article with the relatively hot vapor of the solvent composition, preferably by exposing the article to a solvent vapor rinse from the hot / boiling solvent associated with the first mentioned soaking step. A step of causing the This preferably condenses the solvent vapor on the article. In some preferred embodiments, the distilled solvent can be sprayed onto the article prior to the final rinse.

  It is contemplated that numerous types and types of steam degreasing equipment can be adapted for use with the present method. An example of such an apparatus and its operation is disclosed by Sherliker et al. US Pat. No. 3,085,918, which is hereby incorporated by reference. The apparatus disclosed in Sherlinker et al. Includes a water separator, and other ancillary equipment, for the boiling liquid for containing the solvent composition, for the cleaning liquid for containing the distilled solvent.

  The cleaning method also includes immersing the contaminated article in a fluid composition of the invention under ambient or room temperature conditions, or with a rag or similar object soaked in a solvent under such conditions. A room temperature wash can be included.

Some preferred cleaning methods include flushing the substrate with the composition according to the invention.
D. Flammability reduction method:
According to some other preferred embodiments, the present invention provides a method of reducing the flammability of a fluid comprising adding a compound or composition of the present invention to the fluid. Flammability for any wide range of flammable fluids can be reduced by the present invention. For example, ethylene oxide, flammable hydrofluorocarbons and hydrocarbons such as HFC-152a, 1,1,1-trifluoroethane (HFC-143a), difluoromethane (HFC-32), propane, hexane, octane, etc. Flammability associated with fluids can be reduced by the present invention. For example, in some compositions according to the present invention, CF ₃ I and HFC-152a may be greater than 0 and up to about 38.5% CF ₃ I, more preferably, based on the combined weight of these two components. Can be included in amounts of greater than 0 to about 35% CF ₃ I, and from about 61.5 to less than about 100, and even more preferably from about 65 to less than about 100 HFC-152a. For the purposes of the present invention, a flammable fluid is any fluid that exhibits a flammable range in air as measured by any standard conventional test method such as ASTM-E-681. Good.

  In accordance with the present invention, any suitable amount of the compound or composition can be added to reduce the flammability of the fluid. As will be appreciated by those skilled in the art, the amount added will depend, at least in part, on the degree of flammability of the subject fluid and the degree to which it is desired to reduce its flammability. In some preferred embodiments, the amount of compound or composition added to the flammable fluid is effective to render the resulting fluid substantially non-flammable.

E. Flame suppression method:
The present invention further provides a method of suppressing a flame comprising contacting the flame with a fluid comprising a compound or composition of the present invention. Any suitable method can be used to contact the flame with the present composition. For example, the composition of the present invention can be sprayed, poured, etc. on the flame, or at least a portion of the flame can be immersed in the composition. In view of the teachings herein, one of ordinary skill in the art will readily be able to apply a variety of conventional flame suppression devices and methods for use in the present invention.

F. Sterilization method:
Many articles, instruments, and materials, particularly for use in the medical field, must be sterilized before use for health and safety reasons such as the health and safety of patients and hospital staff. The present invention provides a sterilization method comprising contacting an article, instrument, or material to be sterilized with a compound or composition of the present invention. Such a method may be either a high temperature or low temperature sterilization method. In some embodiments, high temperature sterilization involves the sterilization of the compound, instrument, or material to be sterilized at a temperature of about 250 ° F. to about 270 ° F., preferably in a substantially sealed chamber, or Exposure to a hot fluid containing the composition. This process can usually be completed in less than about 2 hours. However, some articles, such as plastic articles and electrical components, cannot withstand such high temperatures and require low temperature sterilization.

  Pasteurization of the present invention involves using a compound or composition of the present invention at a temperature of about 100 to about 200 ° F. The compounds of the present invention can be mixed with other conventional chemical sterilants such as ethylene oxide (EO), formaldehyde, hydrogen peroxide, chlorine dioxide, and ozone to form the sterilant compositions of the present invention. it can.

  The pasteurization of the present invention is preferably an at least two-step process performed in a substantially sealed, preferably airtight chamber. In the first step (sterilization step), an article that has been cleaned and encapsulated in a gas-permeable bag is placed in the chamber. The air is then evacuated from the chamber by pulling a vacuum and possibly replacing the air with water vapor. In some embodiments, it is preferred to inject water vapor into the chamber to achieve a relative humidity, preferably in the range of about 30% to about 70%. Such humidity can maximize the sterilization effect of the sterilant introduced into the chamber after the desired relative humidity is achieved. After sufficient time for the sterilant to pass through the encapsulation and reach the gap in the article, the sterilant and water vapor are evacuated from the chamber.

  In a preferred second step (aeration step) of the process, the article is aerated to remove sterilant residues. Removing such residues is particularly important in the case of toxic sterilants, but is optional when using substantially non-toxic compounds of the invention. Exemplary aeration processes include air scrubbing, continuous aeration, and combinations of the two. Air scrubbing is a batch process that typically involves evacuating the chamber for a relatively short period of time, eg, 12 minutes, and then introducing air into the chamber above atmospheric pressure. This cycle is repeated any number of times until the desired removal of sterilant is achieved. Continuous ventilation usually involves introducing air through the inlet on one side of the chamber and then extracting it through the outlet on the other side of the chamber by applying a slight vacuum at the outlet. Often these two approaches are combined. For example, a typical approach involves performing an air wash followed by an aeration cycle.

G. Stabilization method:
The present invention further provides a method for stabilizing a composition comprising an iodocarbon such as trifluoroiodomethane. Preferred method steps include providing at least one iodocarbon compound and stabilizing the at least one iodocarbon compound by exposing the compound to one or more diene-based compounds of the present invention. . In many embodiments, the step of providing iodocarbon provides a composition, such as the specific types of compositions described above, preferably by mixing an effective amount of the stabilizer composition of the present invention with the iodocarbon composition. Adding such a diene-based compound of the invention to such a composition.

H. Supercritical method:
In general, it is believed that many of the uses and methods described herein can be carried out with the present compositions in a supercritical or near supercritical state. For example, in particular, alkaloids (usually derived from plant sources) such as substances such as caffeine, codeine, and papaverine, organometallic materials such as metallocenes that are generally useful as catalysts, and perfumes such as jasmon The composition can be utilized in the solvent and solvent extraction applications described herein for use with flavors.

  The present compositions can be used in connection with a process comprising depositing a catalyst, in particular an organometallic catalyst, on a solid support, preferably in their supercritical or near supercritical state. In one preferred embodiment, these methods preferably include the step of producing finely divided catalyst particles by precipitating such catalyst particles from the composition in a supercritical or near supercritical state. In some preferred embodiments, the catalyst produced according to the present process is expected to exhibit excellent activity.

  It is also contemplated that the pulverized form of the drug can be used in some of the MDI methods and devices described herein, and in such circumstances, the present invention preferably is preferably supercritical or It is intended to provide a method comprising the step of introducing finely divided drug particles, such as albuterol, into the fluid by dissolving such particles in the near supercritical state of the composition. If the material is relatively low when the fluid is in a supercritical or near supercritical state, it may be preferable to use an additive solvent such as an alcohol.

Also, the present supercritical or near supercritical composition can be used to clean circuit boards and other electronic materials and articles.
Some materials may have very limited solubility in the present composition, especially when in the supercritical or near supercritical state. For such situations, the composition can be used as an antisolvent to precipitate such low solubility solutes from solutions in other supercritical or near supercritical solvents such as carbon dioxide. For example, supercritical carbon dioxide is often used in thermoplastic foam extrusion processes, and the composition can be used to precipitate some materials contained therein.

  It is also contemplated that in some embodiments it may be desirable to utilize the present supercritical or near supercritical composition as a blowing agent.

The following examples further illustrate the present application, but these are illustrative and are not intended to be limiting in any way.
Example I:
Example I-1:
This example shows a stabilized composition of the present invention comprising CF ₃ I, PAG oil, and isoprene.

  A mixture (1.6 g) of trifluoroiodomethane (25 wt%) and HFO-1234yf (75 wt%) was added to 3 g of the composition containing 99 wt% PAG oil and 1 wt% isoprene. The resulting mixture was placed in a glass tube with aluminum, steel and copper pieces and then the tube was sealed. The sealed glass tube was placed in a 300 ° F. oven for 2 weeks. After this time, the tube was removed and observed.

  Observations showed that the mixture was one phase, indicating that the refrigerant remained miscible and soluble in the PAG oil during this time. Furthermore, the liquid in the tube was a clear light yellow. The appearance of the steel piece was not changed.

  The glass tube was opened and the gas was extracted. The gas was tested by gas chromatography for the presence of trifluoromethane (HFC-23), a decomposition product of oil that reacted with trifluoroiodide. The confirmed HFC-23 level was about 0.23 ± 0.07 wt%.

Example I-2:
This example shows a stabilized composition of the present invention comprising CF ₃ I, PAG oil, and myrcene.
A mixture of trifluoroiodomethane (25 wt%) and HFO-1234yf (75 wt%) (1.6 g) was added to 3 g of the composition containing 99 wt% PAG oil and 1 wt% myrcene. The resulting mixture was placed in a glass tube with aluminum, steel and copper pieces and then the tube was sealed. The sealed glass tube was placed in a 300 ° F. oven for 2 weeks. After such time, the tube was removed and observed.

  Observations showed that the mixture was one phase, indicating that the refrigerant remained miscible and soluble in the PAG oil during this time. Furthermore, the liquid in the tube was a clear light yellow. The appearance of the steel piece was not changed.

  The glass tube was opened and the gas was extracted. The gas was tested by gas chromatography for the presence of trifluoromethane (HFC-23), a decomposition product of oil that reacted with trifluoroiodide. The confirmed level of HFC-23 was 0.27% by weight. When the experiment was repeated, the result was 0.28 wt% HFC-23.

Example I-3:
This example shows a stabilized composition of the present invention comprising CF ₃ I, PAG oil, and farnesol.

  A mixture of trifluoroiodomethane (25 wt%) and HFO-1234yf (75 wt%) (1.6 g) was added to 3 g of the composition containing 99 wt% PAG and 1 wt% farnesol. The resulting mixture was placed in a glass tube with aluminum, steel and copper pieces and then the tube was sealed. The sealed glass tube was placed in a 300 ° F. oven for 2 weeks. After such time, the tube was removed and observed.

  Observations showed that the mixture was one phase, indicating that the refrigerant remained miscible and soluble in the PAG oil during this time. Furthermore, the liquid in the tube was a clear light yellow. The appearance of the steel piece was not changed.

  The glass tube was opened and the gas was extracted. The gas was tested by gas chromatography for the presence of trifluoromethane (HFC-23), a decomposition product of oil that reacted with trifluoroiodide. The level of HFC-23 identified was 0.16% by weight.

Example I-4:
This example shows a stabilized composition of the present invention comprising CF ₃ I, PAG oil, and geraniol.

  A mixture of trifluoroiodomethane (25 wt%) and HFO-1234yf (75 wt%) (1.6 g) was added to 3 g of the composition containing 99 wt% PAG oil and 1 wt% geraniol. The resulting mixture was placed in a glass tube with aluminum, steel and copper pieces and then the tube was sealed. The sealed glass tube was placed in a 300 ° F. oven for 2 weeks. After such time, the tube was removed and observed.

  Observations showed that the mixture was one phase, indicating that the refrigerant remained miscible and soluble in the PAG oil during this time. Furthermore, the liquid in the tube was a clear light yellow. The appearance of the steel piece was not changed.

  The glass tube was opened and the gas was extracted. The gas was tested by gas chromatography for the presence of trifluoromethane (HFC-23), a decomposition product of oil that reacted with trifluoroiodide. The confirmed HFC-23 level was 0.14% by weight.

Example I-5:
This example illustrates a stabilized composition of the present invention comprising CF ₃ I, a polyalkylene glycol lubricant, and myrcene with triphenyl phosphite (DP-213, available from Dover Chemical) as an additive in oil. Indicates.

  A mixture (1.6 g) of trifluoroiodomethane (about 9 wt%) and HFO-1234yf (about 91 wt%) is commercially available as 99 wt% polyalkylene glycol lubricant (Motorcraft PAG Refrigerant Compressor Oil) ) And 3 g of the composition containing 1 wt% additive as described in the paragraph above. The resulting mixture was placed in a glass tube with aluminum, steel and copper pieces and then the tube was sealed. The sealed glass tube was placed in a 300 ° F. oven for 2 weeks. After such time, the tube was removed and observed.

  Observations showed that the mixture was one phase, indicating that the iodocarbon compound remained miscible and soluble in the PAG oil during this time. Furthermore, the liquid in the tube was a clear light yellow. The appearance of the steel piece was not changed.

  The glass tube was opened and the gas was extracted. The gas was tested by gas chromatography for the presence of HFC-23, an oil breakdown product that reacted with trifluoroiodide. The confirmed HFC-23 level was about 0.2% by weight.

Example I-6:
This example shows a stabilized composition of the present invention comprising a stabilizer composed of CF ₃ I and a polyalkylene glycol lubricant, and myrcene.

  Trifluoroiodomethane (1.6 g) was added to 3 g of polyalkylene glycol lubricant containing myrcene (myrcene is present in an amount of 1% by weight, based on the total weight of the lubricant). The resulting mixture was placed in a glass tube with aluminum, steel and copper pieces and then the tube was sealed. The sealed glass tube was placed in a 300 ° F. oven for 2 weeks. After such time, the tube was removed and observed.

  Observations showed that the mixture was a single phase, indicating that the refrigerant was miscible and soluble in PAG oil. Furthermore, the liquid in the tube was a clear light yellow. The appearance of the steel piece was not changed.

  The glass tube was opened and the gas was extracted. The gas was tested by gas chromatography for the presence of trifluoromethane (HFC-23), a decomposition product of oil that reacted with trifluoroiodide. The level of HFC-23 identified was 0.23% by weight.

Example I-7:
This example shows that the level of CF ₃ I degradation in mineral oil is dramatically reduced by the combination of the additives myrcene and Doverphos DP213.

  A mixture (1.6 g) of trifluoroiodomethane (25 wt%) and HFO-1234yf (75 wt%) was added to 3 g of mineral oil. The mineral oil contained 0.5% by weight myrcene and 0.5% by weight Doverphos DP-213. The resulting mixture was placed in a glass tube with aluminum, steel and copper pieces and then the tube was sealed. The sealed glass tube was placed in a 300 ° F. oven for 2 weeks. After such time, the tube was removed.

  The glass tube was opened and the gas was extracted. The gas was tested by gas chromatography for the presence of trifluoromethane (HFC-23), a decomposition product of oil that reacted with trifluoroiodide. The level of HFC-23 identified was 0.08% by weight. When the experiment was repeated, the result was 0.08 wt% HFC-23.

Comparative Example I-1:
A mixture (1.6 g) of trifluoroiodomethane (about 9 wt%) and HFO-1234yf (about 91 wt%) is commercially available as 99 wt% polyalkylene glycol lubricant (Motorcraft PAG Refrigerant Compressor Oil) ) Was added to 3 g of the composition. No stabilizer additive was used. The resulting mixture was placed in a glass tube with aluminum, steel and copper pieces and then the tube was sealed. The sealed glass tube was placed in a 300 ° F. oven for 2 weeks. After such time, the tube was removed and observed.

  Observations showed that the mixture was one phase, which indicated that the refrigerant composition remained miscible and soluble in mineral oil during this time. After exposure, the metal pieces changed color and the lubricant color was dark brown.

  The glass tube was opened and the gas was extracted. The gas was tested by gas chromatography for the presence of HFC-23, an oil breakdown product that reacted with trifluoroiodide. The confirmed level of HFC-23 was about 1.0% by weight.

Comparative Example I-2:
A mixture (1.6 g) of trifluoroiodomethane (25 wt%) and HFO-1234yf (75 wt%) was added to 3 g of mineral oil. The resulting mixture was placed in a glass tube with aluminum, steel and copper pieces and then the tube was sealed. The sealed glass tube was placed in a 300 ° F. oven for 2 weeks.

  After 2 weeks of exposure, the glass tube was opened and the gas was evacuated. The gas was tested by gas chromatography for the presence of trifluoromethane (HFC-23), a decomposition product of oil that reacted with trifluoroiodide. The confirmed level of HFC-23 was 0.76% by weight. When the experiment was repeated, the result was 1.51 wt% HFC-23.

Example II:
This example shows a stabilized composition of the present invention comprising a 30/70 blend of CF ₃ I / HFO-1234yf, PAG oil (RL-897), and a stabilizing compound. 4 g of RL-897 and 1.62 g of CF ₃ I / HFO-1234yf blend were placed in a sealed glass tube with a metal assembly formed of aluminum, steel, and copper. The sealed tube was placed in an oven at 300 ° C. for 2 weeks. The tube was removed from the oven, cooled, opened and the gas was withdrawn.

In these conditions, degradation products of CF ₃ I is R-23 in the gas phase. Therefore, the gas was analyzed for the amount of R23 therein. In addition, a standard test without additives was also tested.

Since interest is the degradation of CF ₃ I, 1% additives in the oil were tested for their effect on the level of degradation products. The results are shown in Table I below.

Phosphate stabilizers, 2,4-dimethyl -6-tert-butylphenol, allyl glycidyl ether, tocopherol, and results for hexane glycidyl _{ether, CF 3 I / HFO-1234yf} CF 3 I R23 into the 30/70 blend of It shows that the decomposition of is reduced. The results for the stabilizers myrcene, geraniol, farnesol, limonene, diphenyl phosphate, 1,2-epoxyhexene, dilauryl hydrogen showed that the degradation of CF ₃ I to R23 was greatly reduced.

Example III:
This example shows a stabilized composition of the present invention comprising a 30/70 blend of CF ₃ I / HFC-32, PAG oil (ND-8), and a stabilizing compound. 2 g of ND-8 and 2 g of CF ₃ I / HFC-32 blend were placed in a sealed glass tube together with a metal assembly formed of aluminum, steel, and copper. The sealed tube was placed in an oven at 300 ° C. for 1 week. The tube was removed from the oven, cooled, opened and the gas was withdrawn.

Under these conditions, CF ₃ I decomposition products are gas phase R-23 and iodide ions in oil. The oil was therefore analyzed for the amount of iodide in it. The gas was analyzed for the amount of R23 in it.

30/70 In addition to the blends _were tested for 10/90 blend of CF 3 I / HFC-32. A baseline test was performed for each blend with no additive. Since interest is the degradation of CF ₃ I, 1% additives in the oil were tested for their effect on the level of degradation products. The results are shown in Tables II and III below.

  The baseline for the 30/70 blend gave 0.73% R23 and 195 ppm iodide concentration. For the three comparative additives, the amount of R23 produced was higher, indicating that some additives may be harmful. The corresponding iodide concentration was greater or not significantly reduced.

Farnesol stabilizers, myrcene, butadiene, and a naphthyl glycidyl ether _results indicate that the degradation of the R23 of CF ₃ I in 30/70 blend of CF 3 I / HFC-32 is substantially reduced. Similarly, the iodide concentration was much lower than when no additive was used or when one of the comparative samples was used.

（式中、
Ｒ^１は、少なくとも３個の炭素原子を有する脂肪族基であり；
Ｒ^２は、４又は５個の炭素原子を有する脂肪族基、又は多環式芳香族基である）
にしたがう化合物から選択されるエポキシ化合物；
（３）下式Ｐ１：

（式中、それぞれのＲは、独立して、フェニル基、又は少なくとも６個であるが１５個未満の炭素原子を有するカルボキシレート基である）
にしたがうホスファイト；
（４）非ヒンダード又は弱ヒンダードフェノール類；及び
（５）これらの任意の２以上の組み合わせ；
からなる群から選択され、少なくとも１種類のヨードカーボンを劣化に対して安定化させるのに有効な量で存在する少なくとも１種類の安定化化合物；
を含む熱伝達組成物。
［２］
Ｒ^１が４〜６個の炭素原子を有する不飽和脂肪族基であり、Ｒ^２がナフチル基であり、少なくとも１種類のヨードカーボンがＣＦ_３Ｉを含む、［１］に記載の熱伝達組成物。
［３］
安定化化合物が、（１）少なくとも２つの炭素−炭素二重結合及び少なくとも４個の炭素原子を有するジエンベースの化合物；（２）式（Ｅ１）及び（Ｅ２）：

（式中、
Ｒ^１は、少なくとも３個の炭素原子を有する脂肪族基であり；
Ｒ^２は、４又は５個の炭素原子を有する脂肪族基、又は多環式芳香族基である）
にしたがう化合物から選択されるエポキシ化合物；
（３）下式Ｐ１：

（式中、それぞれのＲは、独立して、フェニル基、又は少なくとも６個であるが１５個未満の炭素原子を有するカルボキシレート基である）
にしたがうホスファイト；
及び（１）〜（３）の任意の２以上の組み合わせ；
からなる群から選択される、［１］に記載の組成物。
［４］
安定化化合物が、ミルセン、ゲラニオール、ファルネソール、リモネン、ジフェニルホスファイト、１，２−エポキシヘキセン、ジラウリルハイドロジェンホスファイト、２，４−ジメチル−６−ｔｅｒｔ−ブチルフェノール、トコフェロール、及びこれらの２以上の組み合わせからなる群から選択される、［１］に記載の組成物。
［５］
（ａ）少なくとも１種類のヨードカーボン；
（ｂ）該ヨードカーボン以外の少なくとも１種類の冷媒化合物；
（ｃ）ポリアルキレングリコール（ＰＡＧ）を含む少なくとも１種類の潤滑剤；
（ｄ）ジエンベースの化合物、エポキシド類、ホスフェート類、ホスファイト類、及びこれらの組み合わせからなる群から選択される少なくとも１種類の安定化化合物；
を含む熱伝達組成物。
［６］
少なくとも１種類の安定化化合物が、熱伝達組成物に関する使用条件下において少なくとも１種類のヨードカーボンを劣化に対して安定化させるのに有効な量で組成物中に存在する、［５］に記載の組成物。
［７］
ジエンベースの化合物がブタジエンを含む、［５］に記載の組成物。
［８］
ジエンベースの化合物が、ミルセン、ゲラニオール、ファルネソール、リモネン、及びこれらの組み合わせからなる群から選択される少なくとも１種類のテルペンベースの化合物を含む、［７］に記載の組成物。
［９］
安定化化合物が、１，２−エポキシヘキサン、ナフチルグリシジルエーテル、及びこれらの組み合わせからなる群から選択されるエポキシド類を含む、［５］に記載の組成物。
［１０］
（ａ）ポリアルキレングリコール（ＰＡＧ）を含む少なくとも１種類の潤滑剤；
（ｂ）（１）少なくとも２つの炭素−炭素二重結合及び少なくとも４個の炭素原子を有するジエンベースの化合物；（２）式（Ｅ１）及び（Ｅ２）：

（式中、
Ｒ^１は、少なくとも３個の炭素原子を有する脂肪族基であり；
Ｒ^２は、４又は５個の炭素原子を有する脂肪族基、又は多環式芳香族基である）
にしたがう化合物から選択されるエポキシ化合物；
（３）下式Ｐ１：

（式中、それぞれのＲは、独立して、フェニル基、又は少なくとも６個であるが１５個未満の炭素原子を有するカルボキシレート基である）
にしたがうホスファイト；
（４）非ヒンダード又は弱ヒンダードフェノール類；及び
（５）これらの任意の２以上の組み合わせ；
からなる群から選択される少なくとも１種類の安定化化合物；
を含む、熱伝達システムにおいて用いるための潤滑油組成物。 Results for farnesol used in the 10/90 blend of CF ₃ I / HFC-32 shows that both the concentration of R23 and iodide is reduced.
The present invention includes the following aspects.
[1]
(A) at least one iodocarbon;
(B) at least one refrigerant compound other than the iodocarbon; and (c) (1) a diene-based compound having at least two carbon-carbon double bonds and at least four carbon atoms; E1) and (E2):

(Where
R ¹ is an aliphatic group having at least 3 carbon atoms;
R ² is an aliphatic group having 4 or 5 carbon atoms, or a polycyclic aromatic group)
An epoxy compound selected from compounds according to:
(3) The following formula P1:

Wherein each R is independently a phenyl group or a carboxylate group having at least 6 but less than 15 carbon atoms.
Phosphite according to
(4) non-hindered or weakly hindered phenols; and (5) any two or more combinations thereof;
At least one stabilizing compound present in an amount effective to stabilize at least one iodocarbon against degradation, selected from the group consisting of:
A heat transfer composition comprising:
[2]
The heat transfer composition according to [1], wherein R ¹ is an unsaturated aliphatic group having 4 to 6 carbon atoms, R ² is a naphthyl group, and at least one kind of iodocarbon contains CF ₃ I. object.
[3]
The stabilizing compound is (1) a diene-based compound having at least 2 carbon-carbon double bonds and at least 4 carbon atoms; (2) Formulas (E1) and (E2):

(Where
R ¹ is an aliphatic group having at least 3 carbon atoms;
R ² is an aliphatic group having 4 or 5 carbon atoms, or a polycyclic aromatic group)
An epoxy compound selected from compounds according to:
(3) The following formula P1:

Wherein each R is independently a phenyl group or a carboxylate group having at least 6 but less than 15 carbon atoms.
Phosphite according to
And any two or more combinations of (1) to (3);
The composition according to [1], which is selected from the group consisting of:
[4]
The stabilizing compound is myrcene, geraniol, farnesol, limonene, diphenyl phosphite, 1,2-epoxyhexene, dilauryl hydrogen phosphite, 2,4-dimethyl-6-tert-butylphenol, tocopherol, and two or more thereof The composition according to [1], which is selected from the group consisting of:
[5]
(A) at least one iodocarbon;
(B) at least one refrigerant compound other than the iodocarbon;
(C) at least one lubricant comprising polyalkylene glycol (PAG);
(D) at least one stabilizing compound selected from the group consisting of diene-based compounds, epoxides, phosphates, phosphites, and combinations thereof;
A heat transfer composition comprising:
[6]
[5] The at least one stabilizing compound is present in the composition in an amount effective to stabilize at least one iodocarbon against degradation under the conditions of use for the heat transfer composition. Composition.
[7]
The composition according to [5], wherein the diene-based compound comprises butadiene.
[8]
The composition of [7], wherein the diene-based compound comprises at least one terpene-based compound selected from the group consisting of myrcene, geraniol, farnesol, limonene, and combinations thereof.
[9]
The composition of [5], wherein the stabilizing compound comprises epoxides selected from the group consisting of 1,2-epoxyhexane, naphthyl glycidyl ether, and combinations thereof.
[10]
(A) at least one lubricant comprising polyalkylene glycol (PAG);
(B) (1) diene-based compounds having at least two carbon-carbon double bonds and at least four carbon atoms; (2) Formulas (E1) and (E2):

(Where
R ¹ is an aliphatic group having at least 3 carbon atoms;
R ² is an aliphatic group having 4 or 5 carbon atoms, or a polycyclic aromatic group)
An epoxy compound selected from compounds according to:
(3) The following formula P1:

Wherein each R is independently a phenyl group or a carboxylate group having at least 6 but less than 15 carbon atoms.
Phosphite according to
(4) non-hindered or weakly hindered phenols; and (5) any two or more combinations thereof;
At least one stabilizing compound selected from the group consisting of:
A lubricating oil composition for use in a heat transfer system.

Claims (15)

(A) 5 to 50 wt% of _CF 3 I;
(B) 50-95% by weight of hydrofluorocarbon (HFC);
(C) a stabilizing compound comprising both a sesquiterpene compound and a phosphate or phosphite compound, wherein the sesquiterpene compound is selected from farnesol or farnesene, and the phosphate or phosphite compound is diphenyl phosphate, diphenyl phosphite, triphenyl A stabilizing compound selected from phosphate and triphenyl phosphite and present in an amount of 0.001 to 15% by weight; and (d) at least one lubricant;
A heat transfer composition comprising: The composition of claim 1 containing 20 to 40 wt% of CF ₃ I. The composition of claim 1 containing 25 to 35 wt% of CF ₃ I.   4. A composition according to any one of claims 1 to 3 comprising 60 to 80 wt% HFC.   4. A composition according to any one of claims 1 to 3 comprising 65 to 75 wt% HFC.   HFC is difluoromethane (HFC-32); pentafluoroethane (HFC-125); 1,1,2,2-tetrafluoroethane (HFC-134); 1,1,1,2-tetrafluoroethane (HFC) -134a): trifluoroethane (HFC-143a); difluoroethane (HFC-152a); 1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea); 1,1,1,3 , 3,3-hexafluoropropane (HFC-236fa); 1,1,1,3,3-pentafluoropropane (HFC-245fa); and 1,1,1,3,3-pentafluorobutane (HFC-) The composition according to claim 1, which is one or more compounds selected from 365 mfc).   The composition of claim 6, wherein the one or more compounds is at least difluoromethane (HFC-32). The composition according to claim 1, wherein the stabilizing compound is farnesene and diphenyl phosphite . Farnesene is α-farnesene (ie, 3,7,11-trimethyldoscadedodec-1,3,6,19-tetraene) or β-farnesene (ie, 7,11-dimethyl-3-methylene-1,6). , 10- dodecatriene) (a including all such stereoisomers) the composition according to claim 1. Lubricant comprises a polyalkylene glycol (PAG), A composition according to any one of claims 1-9. (A) 5 to 50 wt% of _CF 3 I;
(B) 50-95% by weight of at least one hydrofluorocarbon (HFC) comprising at least difluoromethane (HFC-32);
(C) a stabilizing compound comprising both a sesquiterpene compound and a phosphate or phosphite compound, wherein the sesquiterpene compound is selected from farnesol or farnesene, and the phosphate or phosphite compound is diphenyl phosphate, diphenyl phosphite, triphenyl A stabilizing compound selected from phosphate and triphenyl phosphite and present in an amount of 0.001 to 15% by weight ; and (d) at least one lubricant comprising polyalkylene glycol (PAG);
The heat transfer composition comprising a. (A) 5 to 50 wt% of _CF 3 I;
(B) 50-95% by weight of at least one hydrofluorocarbon (HFC) comprising at least difluoromethane (HFC-32);
(C) a first stabilizing compound comprising farnesene and a second stabilizing compound comprising diphenyl phosphite; and (d) at least one lubricant comprising polyalkylene glycol (PAG);
Wherein the stabilizing compound is present in an amount of 0.5-2% by weight. The composition has a global warming potential of less than 1000 (GWP), A composition according to any one of claims 1 to 12. 14. A composition according to any of claims 1 to 13 , wherein the composition has a global warming potential (GWP) of less than 150. The heat transfer composition according to any one of claims 1 to 14 , in an automotive air conditioning system and device, a commercial cooling system and device, a chiller, a residential refrigerator and freezer, a general air conditioning system, a heat pump, ORC or CRC. Use of.