Azeotrope and Azeotrope-like Compositions Comprising Neopentane and Isomers of HFO-1336mzz

Information

  • Patent Application
  • 20230332031
  • Publication Number
    20230332031
  • Date Filed
    October 08, 2020
    3 years ago
  • Date Published
    October 19, 2023
    6 months ago
Abstract
The present application relates to azeotrope and azeotrope-like compositions comprising neopentane and a compound selected from E-1,1,1,4,4,4-hexafluoro-2-butene (HFO-1336mzz(E)) and Z-1,1,1,4,4,4-hexafluoro-2-butene (HFO-1336mzz(Z)). Methods of using the compositions of the invention in propellant applications, heat transfer applications, and refrigeration applications are also provided.
Description
TECHNICAL FIELD

The present application relates to azeotrope and azeotrope-like compositions comprising neopentane and a compound selected from E-1,1,1,4,4,4-hexafluoro-2-butene (HFO-1336mzz(E)) and Z-1,1,1,4,4,4-hexafluoro-2-butene (HFO-1336mzz(Z)). The compositions described herein may be useful in a variety of 61 applications including, but not limited to, heat transfer applications, and refrigeration applications.


BACKGROUND

Many industries have been working for the past few decades to find replacements for the ozone depleting chlorofluorocarbons (CFCs) and hydrochlorofluorocarbons (HCFCs). The CFCs and HCFCs have been employed in a wide range of applications, including their use, for example, as aerosol propellants, refrigerants and heat transfer media. In the search for replacements for these versatile compounds, many industries have turned to the use of hydrofluoroolefins (HFOs).


SUMMARY

The present application provides, inter alia, compositions comprising:

    • i) neopentane 2,2-dimethylpropane); and
    • ii) a compound selected from E-1,1,1,4,4,4-hexafluoro-2-butene HFO-1336mzz(E)) and Z-1,1,1,4,4,4-hexafluoro-2-butene HFO-1336mzz(Z)),
    • wherein the E-1,1,1,4,4,4-hexafluoro-2-butene or Z-1,1,1,4,4,4-hexafluoro-2-butene is present in the composition in an amount effective to form an azeotrope composition or an azeotrope-like composition with the neopentane.


The present application further provides methods of using the compositions provided herein as propellants and heat transfer agents (e.g., in refrigeration or heat transfer applications).


Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Methods and materials are described herein for use in the present invention; other, suitable methods and materials known in the art can also be used. The materials, methods, and examples are illustrative only and not intended to be limiting. All publications, patent applications, patents, sequences, database entries, and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will control.





DESCRIPTION OF DRAWINGS


FIG. 1 displays the vapor/liquid equilibrium curve for a mixture of E-HFO-1336mzz and neopentane at a temperature of 29.88° C., and shows the formation of an azeotrope of composition 0.552 mole fraction E-HFO-1336mzz and 0.448 mole fraction neopentane, which has a vapor pressure of 41.8 psia.



FIG. 2 displays the vapor/liquid equilibrium curve for a mixture of Z-HFO-1336mzz and neopentane at a temperature of 29.90° C., and shows the formation of an azeotrope of composition 0.220 mole fraction Z-HFO-1336mzz and 0.780 mole fraction neopentane, which has a vapor pressure of 31.8 psia.





DETAILED DESCRIPTION

The present application provides compositions comprising:

    • i) neopentane 2,2-dimethylpropane); and
    • ii) a compound selected from E-1,1,1,4,4,4-hexafluoro-2-butene HFO-1336mzz(E)) and Z-1,1,1,4,4,4-hexafluoro-2-butene HFO-1336mzz(Z)),
    • wherein the E-1,1,1,4,4,4-hexafluoro-2-butene or Z-1,1,1,4,4,4-hexafluoro-2-butene is present in the composition in an amount effective to form an azeotrope composition or an azeotrope-like composition with the neopentane.


Definitions and Abbreviations

As used herein, the terms “comprises,” “comprising,” “includes,” “including,” “has,” “having” or any other variation thereof, are intended to cover a non-exclusive inclusion. For example, a process, method, article, or apparatus that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. Further, unless expressly stated to the contrary, “or” refers to an inclusive or and not to an exclusive or. For example, a condition A or B is satisfied by any one of the following: A is true (or present) and B is false (or not present), A is false (or not present) and B is true (or present), and both A and B are true (or present).


As used herein, the term “consisting essentially of” is used to define a composition, method that includes materials, steps, features, components, or elements, in addition to those literally disclosed provided that these additional included materials, steps, features, components, or elements do not materially affect the basic and novel characteristic(s) of the claimed invention, especially the mode of action to achieve the desired result of any of the processes of the present invention. The term “consists essentially of” or “consisting essentially of” occupies a middle ground between “comprising” and “consisting of”.


For example, in some embodiments the composition provided herein consists essentially of:

    • i) neopentane;
    • ii) a compound selected from E-1,1,1,4,4,4-hexafluoro-2-butene (HFO-1336mzz(E)) and Z-1,1,1,4,4,4-hexafluoro-2-butene (HFO-1336mzz(Z)),
    • wherein the E-1,1,1,4,4,4-hexafluoro-2-butene or Z-1,1,1,4,4,4-hexafluoro-2-butene is present in the composition in an amount effective to form an azeotrope composition or an azeotrope-like composition with the neopentane; and
    • iii) one or more additional components as described herein (wherein the one or more additional components do not materially affect the basic and novel characteristic(s) of the composition).


Also, use of “a” or “an” are employed to describe elements and components described herein. This is done merely for convenience and to give a general sense of the scope of the invention. This description should be read to include one or at least one and the singular also includes the plural unless it is obvious that it is meant otherwise.


As used herein, the term “about” is meant to account for variations due to experimental error (e.g., plus or minus approximately 10% of the indicated value). All measurements reported herein are understood to be modified by the term “about”, whether or not the term is explicitly used, unless explicitly stated otherwise.


As used herein, the term “azeotropic composition” refers to a composition where at a given temperature at equilibrium, the boiling point pressure (of the liquid phase) is identical to the dew point pressure (of the vapor phase), i.e., X2=Y2. One way to characterize an azeotropic composition is that the vapor produced by partial evaporation or distillation of the liquid has the same composition as the liquid from which it was evaporated or distilled, that is, the admixture distills/refluxes without compositional change. Constant boiling compositions are characterized as azeotropic because they exhibit either a maximum or minimum boiling point, as compared with that of the non-azeotropic mixtures of the same components. Azeotropic compositions are also characterized by a minimum or a maximum in the vapor pressure of the mixture relative to the vapor pressure of the neat components at a constant temperature.


As used herein, the terms “azeotrope-like composition” and “near-azeotropic composition” refer to a composition wherein the difference between the bubble point pressure (“BP”) and dew point pressure (“DP”) of the composition at a particular temperature is less than or equal to 5 percent based upon the bubble point pressure, i.e., [(BP−DP)/BP]×100≤5. As used herein, the terms “3 percent azeotrope-like composition” and “3 percent near-azeotropic composition” shall be understood to mean a composition wherein the difference between the bubble point pressure (“BP”) and dew point pressure (“DP”) of the composition at a particular temperature is less than or equal to 3 percent based upon the bubble point pressure, i.e., [(BP−DP)/BP]×100≤3.


Binary azeotropic or azeotrope-like compositions of substantially constant-boiling mixtures can be characterized, depending upon the conditions chosen, in a number of ways. For example, it is well known by those skilled in the art, that, at different pressures the composition of a given azeotrope or azeotrope-like composition will vary at least to some degree, as will the boiling point temperature. Thus, an azeotropic or azeotrope-like composition of two compounds represents a unique type of relationship but with a variable composition that depends on temperature and/or pressure. Therefore, compositional ranges, rather than fixed compositions, are often used to define azeotropes and azeotrope-like compositions.


For purposes of this invention, “effective amount” refers to the amount of each component of a composition provided herein which, when combined, results in the formation of an azeotropic or azeotrope-like composition. This definition includes the amounts of each component, which amounts may vary depending on the pressure applied to the composition so long as the azeotropic or azeotrope-like compositions continue to exist at the different pressures, but with possible different boiling points. Therefore, effective amount includes the amounts, such as may be expressed in weight percentages, of each component of the compositions of the instant invention which form azeotropic or azeotrope-like compositions at temperatures or pressures other than as described herein.


As used herein, the term “mole fraction” refers to the ratio of the number of moles of one component in the binary composition to the sum of the numbers of moles of each of the two components in said composition (e.g., X2=m2/(m1+m2).


To determine the relative volatility of any two compounds, a method known as the PTx method can be used. In this procedure, the total absolute pressure in a cell of known volume is measured at a constant temperature for various compositions of the two compounds. Use of the PTx Method is described in detail in “Phase Equilibrium in Process Design”, Wiley-Interscience Publisher, 1970, written by Harold R. Null, on pages 124 to 126; hereby incorporated by reference. The resulting pressure v. liquid composition data are alternately referred to as Vapor Liquid Equilibria data (or “VLE data.”)


These measurements can be converted into equilibrium vapor and liquid compositions in the PTx cell by using an activity coefficient equation model, such as the Non-Random, Two-Liquid (NRTL) equation, to represent liquid phase nonidealities. Use of an activity coefficient equation, such as the NRTL equation is described in detail in “The Properties of Gases and Liquids,” 4th edition, published by McGraw Hill, written by Reid, Prausnitz and Poling, on pages 241 to 387, and in “Phase Equilibria in Chemical Engineering,” published by Butterworth Publishers, 1985, written by Stanley M. Walas, pages 165 to 244. The collection of VLE data, the determination of interaction parameters by regression and the use of an equation of state to predict non-ideal behavior of a system are taught in “Double Azeotropy in Binary Mixtures of NH3 and CHF2CF2,” C.-P. Chai Kao, M. E. Paulaitis, A. Yokozeki, Fluid Phase Equilibria, 127 (1997) 191-203. All of the aforementioned references are hereby incorporated by reference. Without wishing to be bound by any theory or explanation, it is believed that the NRTL equation, together with the PTx cell data, can sufficiently predict the relative volatilities of the compositions provided herein and can therefore predict the behavior of these mixtures in multi-stage separation equipment such as distillation columns.


When an amount, concentration, or other value or parameter is given as either a range, preferred range or a list of upper preferable values and/or lower preferable values, this is to be understood as specifically disclosing all ranges formed from any pair of any upper range limit or preferred value and any lower range limit or preferred value, regardless of whether ranges are separately disclosed. Where a range of numerical values is recited herein, unless otherwise stated, the range is intended to include the endpoints thereof, and all integers and fractions within the range.


Compositions

A composition, comprising:

    • i) neopentane; and
    • ii) a compound selected from E-1,1,1,4,4,4-hexafluoro-2-butene and Z-1,1,1,4,4,4-hexafluoro-2-butene.


In some embodiments, the composition provided herein is an azeotrope or azeotrope-like composition. In some embodiments, the composition provided herein is an azeotrope composition. In some embodiments, the composition provided herein is an azeotrope-like composition. In some embodiments, the E-1,1,1,4,4,4-hexafluoro-2-butene or Z-1,1,1,4,4,4-hexafluoro-2-butene is present in the composition in an amount effective to form an azeotrope composition or an azeotrope-like composition with the neopentane.


In some embodiments, the composition provided herein comprises neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene, wherein the E-1,1,1,4,4,4-hexafluoro-2-butene is present in the composition in an amount effective to form an azeotrope composition or an azeotrope-like composition with the neopentane. In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene is an azeotrope composition (i.e., an azeotropic composition). In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene is an azeotrope-like composition.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 40 to about 60 mol % neopentane, for example, about 40 to about 55, about 40 to about 50, about 40 to about 45, about 45 to about 60, about 45 to about 55, about 45 to about 50, about 50 to about 60, about 50 to about 55, or about 55 to about 60 mol % neopentane. In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 40 to about 50 mol % neopentane.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 60 to about 40 mol % E-1,1,1,4,4,4-hexafluoro-2-butene, for example, about 60 to about 45, about 60 to about 50, about 60 to about 55, about 55 to about 40, about 55 to about 45, about 55 to about 50, about 50 to about 40, about 50 to about 45, or about 45 to about 40 mol % E-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from 60 to about 50 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.


In some embodiments, the composition comprises from about 40 to about 60 mol % neopentane and about 60 to about 40 mol % E-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprises from about 40 to about 60 mol % neopentane and about 60 to about 40 mol % E-1,1,1,4,4,4-hexafluoro-2-butene, and has a boiling point of from about −40° C. to about 120° C. at a pressure of from about 2 psi to about 390 psi.


In some embodiments, the composition comprises from about 40 to about 50 mol % neopentane and about 60 to about 50 mol % E-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprises from about 40 to about 50 mol % neopentane and about 60 to about 50 mol % E-1,1,1,4,4,4-hexafluoro-2-butene, and has a boiling point of from about 0.9° C. to about 128° C. at a pressure of from about 1 atm to about 30 atm.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises 98.0 to about 99.9 mol % neopentane, for example, about 98.0 to about 99.8, about 98.0 to about 99.5, about 98.0 to about 99.3, about 98.0 to about 99.0, about 98.0 to about 98.8, about 98.0 to about 98.5, about 98.5 to about 99.9, about 98.5 to about 99.8, about 98.5 to about 99.5, about 98.5 to about 99.3, about 98.5 to about 99.0, about 98.5 to about 98.8, about 98.8 to about 99.9, about 98.8 to about 99.8, about 98.8 to about 99.5, about 98.8 to about 99.3, about 98.8 to about 99.0, about 99.0 to about 99.9, about 99.0 to about 99.8, about 99.0 to about 99.5, about 99.0 to about 99.3, about 99.3 to about 99.9, about 99.3 to about 99.8, about 99.3 to about 99.5, about 99.5 to about 99.9, about 99.5 to about 99.8, or about 99.8 to about 99.9 mol % neopentane. In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 98.2 to about 99.8 mol % neopentane.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises about 2.0 to about 0.1 mol % E-1,1,1,4,4,4-hexafluoro-2-butene, for example, about 2.0 to about 0.2, about 2.0 to about 0.5, about 2.0 to about 0.7, about 2.0 to about 1.0, about 2.0 to about 1.2, about 2.0 to about 1.5, about 1.5 to about 0.1, about 1.5 to about 0.2, about 1.5 to about 0.5, about 1.5 to about 0.7, about 1.5 to about 1.0, about 1.5 to about 1.2, about 1.2 to about 0.1, about 1.2 to about 0.2, about 1.2 to about 0.5, about 1.2 to about 0.7, about 1.2 to about 1.0, about 1.0 to about 0.1, about 1.0 to about 0.2, about 1.0 to about 0.5, about 1.0 to about 0.7, about 0.7 to about 0.1, about 0.7 to about 0.2, about 0.7 to about 0.5, about 0.5 to about 0.1, about 0.5 to about 0.2, or about 0.2 to about 0.1 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises about 1.6 to about 0.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 98.4 to about 99.8 mol % neopentane and about 1.6 to about 0.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 98.4 to about 99.8 mol % neopentane and about 1.6 to about 0.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene, and has a boiling point of from about 8.3° C. to about 9.3° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 35 to about 65 mol % neopentane, for example, about 35 to about 60, about 35 to about 55, about 35 to about 50, about 35 to about 45, about 35 to about 40, about 40 to about 65, about 40 to about 60, about 40 to about 55, about 40 to about 50, about 40 to about 45, about 45 to about 65, about 45 to about 60, about 45 to about 55, about 45 to about 50, about 50 to about 65, about 50 to about 60, about 50 to about 55, about 55 to about 65, about 55 to about 60, or about 60 to about 65 mol % neopentane. In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 38.4 to about 62.6 mol % neopentane.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 70 to about 35 mol % E-1,1,1,4,4,4-hexafluoro-2-butene, for example, about 70 to about 40, about 70 to about 45, about 70 to about 50, about 70 to about 55, about 70 to about 60, about 70 to about 65, about 65 to about 35, about 65 to about 40, about 65 to about 45, about 65 to about 50, about 65 to about 55, about 65 to about 60, about 60 to about 35, about 60 to about 40, about 60 to about 45, about 60 to about 50, about 60 to about 55, about 55 to about 35, about 55 to about 40, about 55 to about 45, about 55 to about 50, about 50 to about 35, about 50 to about 40, about 50 to about 45, about 45 to about 35, about 45 to about 40, or about 40 to about 35 mol % E-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 65.2 to about 37.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 38.4 to about 62.6 mol % neopentane and about 65.2 to about 37.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 38.4 to about 62.6 mol % neopentane and about 65.2 to about 37.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene, and has a boiling point of from about 0.9° C. to about 1.2° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises about 0.1 to about 3.0 mol % neopentane, for example, about 0.1 to about 2.8, about 0.1 to about 2.5, about 0.1 to about 2.0, about 0.1 to about 1.5, about 0.1 to about 1.0, about 0.1 to about 0.5, about 0.5 to about 3.0, about 0.5 to about 2.8, about 0.5 to about 2.5, about 0.5 to about 2.0, about 0.5 to about 1.5, about 0.5 to about 1.0, about 1.0 to about 3.0, about 1.0 to about 2.8, about 1.0 to about 2.5, about 1.0 to about 2.0, about 1.0 to about 1.5, about 1.5 to about 3.0, about 1.5 to about 2.8, about 1.5 to about 2.5, about 1.5 to about 2.0, about 2.0 to about 3.0, about 2.0 to about 2.8, about 2.0 to about 2.5, about 2.5 to about 3.0, about 2.5 to about 2.8, or about 2.8 to about 3.0 mol % neopentane. In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 0.2 to about 2.8 mol % neopentane.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises about 99.9 to about 97.0 mol % E-1,1,1,4,4,4-hexafluoro-2-butene, for example, about 99.9 to about 97.2, about 99.9 to about 97.5, about 99.9 to about 98.0, about 99.9 to about 98.5, about 99.9 to about 99.0, about 99.9 to about 99.8, about 99.8 to about 97.0, about 99.8 to about 97.2, about 99.8 to about 97.5, about 99.8 to about 98.0, about 99.8 to about 98.5, about 99.8 to about 99.0, about 99.0 to about 97.0, about 99.0 to about 97.2, about 99.0 to about 97.5, about 99.0 to about 98.0, about 99.0 to about 98.5, about 98.5 to about 97.0, about 98.5 to about 97.2, about 98.5 to about 97.5, about 98.5 to about 98.0, about 98.0 to about 97.0, about 98.0 to about 97.2, about 98.0 to about 97.5, about 97.5 to about 97.0, about 97.5 to about 97.2, or about 97.2 to about 97.0 mol % E-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises about 99.8 to about 97.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 0.2 to about 2.8 mol % neopentane and about 99.8 to about 97.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 0.2 to about 2.8 mol % neopentane and about 99.8 to about 97.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene, and has a boiling point of from about 6.3° C. to about 7.4° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises:

    • from about 99.8 to about 98.2 mol % neopentane and about 0.2 to about 1.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 71.6 to about 47.6 mol % neopentane and about 28.4 to about 52.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 1.2 to about 0.2 mol % neopentane and about 98.8 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 98.4 mol % neopentane and about 0.2 to about 1.6 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 66.6 to about 40.8 mol % neopentane and about 33.4 to about 59.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 1.8 to about 0.2 mol % neopentane and about 98.2 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 62.8 to about 35.2 mol % neopentane and about 37.2 to about 64.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 2.6 to about 0.2 mol % neopentane and about 97.4 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 59.8 to about 30.2 mol % neopentane and about 40.2 to about 69.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 3.4 to about 0.2 mol % neopentane and about 96.6 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 58.4 to about 28.2 mol % neopentane and about 41.6 to about 71.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 3.8 to about 0.2 mol % neopentane and about 96.2 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 57.2 to about 26.4 mol % neopentane and about 42.8 to about 73.6 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 4.4 to about 0.2 mol % neopentane and about 95.6 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 55.4 to about 23.6 mol % neopentane and about 44.6 to about 76.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 5.2 to about 99.1 mol % neopentane and about 94.8 to about 0.9 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 98.6 mol % neopentane and about 0.2 to about 1.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 53.8 to about 23.2 mol % neopentane and about 46.2 to about 76.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 5.4 to about 0.2 mol % neopentane and about 94.6 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 56 to about 24.4 mol % neopentane and about 44.0 to about 75.6 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 4.6 to about 0.2 mol % neopentane and about 95.4 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 57.2 to about 3.8 mol % neopentane and about 42.8 to about 96.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 2.6 to about 0.2 mol % neopentane and about 97.4 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene comprises:

    • from about 99.8 to about 98.2 mol % neopentane and about 0.2 to about 1.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 71.6 to about 47.6 mol % neopentane and about 28.4 to about 52.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 1.2 to about 0.2 mol % neopentane and about 98.8 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 98.4 mol % neopentane and about 0.2 to about 1.6 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 66.6 to about 40.8 mol % neopentane and about 33.4 to about 59.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 1.8 to about 0.2 mol % neopentane and about 98.2 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 62.8 to about 35.2 mol % neopentane and about 37.2 to about 64.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 2.6 to about 0.2 mol % neopentane and about 97.4 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 59.8 to about 30.2 mol % neopentane and about 40.2 to about 69.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 3.4 to about 0.2 mol % neopentane and about 96.6 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 58.4 to about 28.2 mol % neopentane and about 41.6 to about 71.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 3.8 to about 0.2 mol % neopentane and about 96.2 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 57.2 to about 26.4 mol % neopentane and about 42.8 to about 73.6 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 4.4 to about 0.2 mol % neopentane and about 95.6 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 55.4 to about 23.6 mol % neopentane and about 44.6 to about 76.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 5.2 to about 99.1 mol % neopentane and about 94.8 to about 0.9 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 98.6 mol % neopentane and about 0.2 to about 1.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 53.8 to about 23.2 mol % neopentane and about 46.2 to about 76.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 5.4 to about 0.2 mol % neopentane and about 94.6 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 56 to about 24.4 mol % neopentane and about 44.0 to about 75.6 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 4.6 to about 0.2 mol % neopentane and about 95.4 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 57.2 to about 3.8 mol % neopentane and about 42.8 to about 96.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 2.6 to about 0.2 mol % neopentane and about 97.4 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene;
    • wherein the composition has a boiling point of from about −40° C. to about 120° C. at a pressure of about 1 atm, for example, about −40° C. to about 100° C., about −40° C. to about 80° C., about −40° C. to about 60° C., about −40° C. to about 40° C., about −40° C. to about 20° C., about −40° C. to about 0° C., about −40° C. to about −20° C., about −20° C. to about 120° C., about −20° C. to about 100° C., about −20° C. to about 80° C., about −20° C. to about 60° C., about −20° C. to about 40° C., about −20° C. to about 20° C., about −20° C. to about 0° C., about 0° C. to about 120° C., about 0° C. to about 100° C., about 0° C. to about 80° C., about 0° C. to about 60° C., about 0° C. to about 40° C., about 0° C. to about 20° C., about 20° C. to about 120° C., about 20° C. to about 100° C., about 20° C. to about 80° C., about 20° C. to about 60° C., about 20° C. to about 40° C., about 40° C. to about 120° C., about 40° C. to about 100° C., about 40° C. to about 80° C., about 40° C. to about 60° C., about 60° C. to about 120° C., about 60° C. to about 100° C., about 60° C. to about 80° C., about 80° C. to about 120° C., about 80° C. to about 100° C., or about 100° C. to about 120° C.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about −40° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about −20° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 0° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 20° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 30° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 40° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 60° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 80° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 100° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 120° C. at a pressure of about 1 atm.


In some embodiments, the composition provided herein comprises neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene, wherein the Z-1,1,1,4,4,4-hexafluoro-2-butene is present in the composition in an amount effective to form an azeotrope composition or an azeotrope-like composition with the neopentane. In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene is an azeotrope composition (i.e., an azeotropic composition). In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene is an azeotrope-like composition.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 60 to about 95 mol % neopentane, for example, about 60 to about 90, about 60 to about 85, about 60 to about 80, about 60 to about 75, about 60 to about 70, about 65 to about 95, about 65 to about 90, about 65 to about 85, about 65 to about 80, about 65 to about 75, about 70 to about 95, about 70 to about 90, about 70 to about 85, about 70 to about 80, about 75 to about 95, about 75 to about 90, about 75 to about 85, about 80 to about 95, about 80 to about 90, or about 85 to about 95 mol % neopentane. In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 60 to about 93 mol % neopentane.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 40 to about 5 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene, for example, about 40 to about 10, about 40 to about 15, about 40 to about 20, about 40 to about 25, about 40 to about 30, about 40 to about 35, about 35 to about 5, about 35 to about 10, about 35 to about 15, about 35 to about 20, about 35 to about 25, about 35 to about 30, about 30 to about 5, about 30 to about 10, about 30 to about 15, about 30 to about 20, about 30 to about 25, about 25 to about 5, about 25 to about 10, about 25 to about 15, about 25 to about 20, about 20 to about 5, about 20 to about 10, about 20 to about 15, about 15 to about 5, about 15 to about 10, or about 10 to about 5 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 40 to about 7 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 60 to about 93 mol % neopentane and about 40 to about 7 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 60 to about 93 mol % neopentane and about 40 to about 7 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene, and has a boiling point of from about −40° C. to about 120° C. at a pressure of from about 1.5 psi to about 310 psi.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 50 to about 85 mol % neopentane, for example, about 50 to about 80, about 50 to about 75, about 50 to about 70, about 50 to about 65, about 50 to about 60, about 50 to about 55, about 55 to about 85, about 55 to about 80, about 55 to about 75, about 55 to about 70, about 55 to about 65, about 55 to about 60, about 60 to about 85, about 60 to about 80, about 60 to about 75, about 60 to about 70, about 60 to about 65, about 65 to about 85, about 65 to about 80, about 65 to about 75, about 65 to about 70, about 70 to about 85, about 70 to about 80, about 70 to about 75, about 75 to about 85, about 75 to about 80, or about 80 to about 85 mol % neopentane. In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 56 to about 83 mol % neopentane.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 50 to about 15 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene, for example, about 50 to about 20, about 50 to about 25, about 50 to about 30, about 50 to about 35, about 50 to about 40, about 50 to about 45, about 45 to about 15, about 45 to about 20, about 45 to about 25, about 45 to about 30, about 45 to about 35, about 45 to about 40, about 40 to about 15, about 40 to about 20, about 40 to about 25, about 40 to about 30, about 40 to about 35, about 35 to about 15, about 35 to about 20, about 35 to about 25, about 35 to about 30, about 30 to about 15, about 30 to about 20, about 30 to about 25, about 25 to about 15, about 25 to about 20, or about 20 to about 15 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 44 to about 17 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 56 to about 83 mol % neopentane and about 44 to about 17 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 56 to about 83 mol % neopentane and about 44 to about 17 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene, and has a boiling point of from about 5° C. to about 145° C. at a pressure of from about 1 atm to about 30 atm.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 99.9 to about 75.0 mol % neopentane, for example, about 99.9 to about 80.0, about 99.9 to about 85.0, about 99.9 to about 90.0, about 99.9 to about 95.0, about 99.9 to about 99.0, about 99.9 to about 99.6, about 99.6 to about 80.0, about 99.6 to about 85.0, about 99.6 to about 90.0, about 99.6 to about 95.0, about 99.6 to about 99.0, about 99.0 to about 80.0, about 99.0 to about 85.0, about 99.0 to about 90.0, about 99.0 to about 95, about 95.0 to about 80.0, about 95.0 to about 85.0, about 95.0 to about 90.0, about 90.0 to about 80.0, about 90.0 to about 85.0, or about 85.0 to about 80.0 mol % neopentane. In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 99.6 to about 79.2 mol % neopentane.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 0.1 to about 25.0 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene, for example, about 0.1 to about 20.0, about 0.1 to about 15.0, about 0.1 to about 10.0, about 0.1 to about 5.0, about 0.1 to about 1.0, about 0.1 to about 0.4, about 0.4 to about 25.0, about 0.4 to about 20.0, about 0.4 to about 15.0, about 0.4 to about 10.0, about 0.4 to about 5.0, about 0.4 to about 1.0, about 1.0 to about 25.0, about 1.0 to about 20.0, about 1.0 to about 15.0, about 1.0 to about 10.0, about 1.0 to about 5.0, about 5.0 to about 25.0, about 5.0 to about 20.0, about 5.0 to about 15.0, about 5.0 to about 10.0, about 10.0 to about 25.0, about 10.0 to about 20.0, about 10.0 to about 15.0, about 15.0 to about 25.0, about 15.0 to about 20.0, or about 20.0 to about 25.0 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 0.4 to about 20.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 99.6 to about 79.2 mol % neopentane and about 0.4 to about 20.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 99.6 to about 79.2 mol % neopentane and about 0.4 to about 20.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene, and has a boiling point of from about 7.8° C. to about 9.4° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 4.0 to about 1.0 mol % neopentane, for example, about 4.0 to about 1.5, about 4.0 to about 2.0, about 4.0 to about 2.5, about 4.0 to about 3.0, about 4.0 to about 3.5, about 3.5 to about 1.0, about 3.5 to about 1.5, about 3.5 to about 2.0, about 3.5 to about 2.5, about 3.5 to about 3.0, about 3.0 to about 1.0, about 3.0 to about 1.5, about 3.0 to about 2.0, about 3.0 to about 2.5, about 2.5 to about 1.0, about 2.5 to about 1.5, about 2.5 to about 2.0, about 2.0 to about 1.0, about 2.0 to about 1.5, or about 1.5 to about 1.0 mol % neopentane. In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 3.2 to about 1.6 mol % neopentane.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 96.0 to about 99.0 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene, for example, about 96.0 to about 98.5, about 96.0 to about 98.0, about 96.0 to about 97.5, about 96.0 to about 97.0, about 96.0 to about 96.5, about 96.5 to about 99.0, about 96.5 to about 98.5, about 96.5 to about 98.0, about 96.5 to about 97.5, about 96.5 to about 97.0, about 97.0 to about 99.0, about 97.0 to about 98.5, about 97.0 to about 98.0, about 97.0 to about 97.5, about 97.5 to about 99.0, about 97.5 to about 98.5, about 97.5 to about 98.0, about 98.0 to about 99.0, about 98.0 to about 98.5, or about 98.5 to about 99.0 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 96.8 to about 98.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 3.2 to about 1.6 mol % neopentane and about 96.8 to about 98.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene. In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises from about 3.2 to about 1.6 mol % neopentane and about 96.8 to about 98.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene, and has a boiling point of from about 32.6° C. to about 33.0° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises:

    • from about 99.8 to about 85.2 mol % neopentane and about 0.2 to about 14.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 80.8 mol % neopentane and about 0.2 to about 19.2 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 76.2 mol % neopentane and about 0.2 to about 23.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 61.8 mol % neopentane and about 0.2 to about 38.2 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 0.4 to about 0.2 mol % neopentane and about 99.6 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 69.8 mol % neopentane and about 0.2 to about 30.2 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 67.6 mol % neopentane and about 0.2 to about 32.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 95.0 mol % neopentane and about 0.2 to about 5 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 86.4 to about 63.6 mol % neopentane and about 13.6 to about 36.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 0.4 to about 0.2 mol % neopentane and about 99.6 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 96.6 mol % neopentane and about 0.2 to about 3.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 80.6 to about 59.6 mol % neopentane and about 19.4 to about 40.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 97.6 mol % neopentane and about 0.2 to about 2.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 74.2 to about 56.0 mol % neopentane and about 25.8 to about 44.0 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 0.2 to about 0.8 mol % neopentane and about 99.2 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 98.2 mol % neopentane and about 0.2 to about 1.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 76.6 to about 50.0 mol % neopentane and about 23.4 to about 50.0 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 1.0 to about 0.2 mol % neopentane and about 99.0 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene comprises:

    • from about 99.8 to about 85.2 mol % neopentane and about 0.2 to about 14.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 80.8 mol % neopentane and about 0.2 to about 19.2 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 76.2 mol % neopentane and about 0.2 to about 23.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 61.8 mol % neopentane and about 0.2 to about 38.2 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 0.4 to about 0.2 mol % neopentane and about 99.6 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 69.8 mol % neopentane and about 0.2 to about 30.2 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 67.6 mol % neopentane and about 0.2 to about 32.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 95.0 mol % neopentane and about 0.2 to about 5 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 86.4 to about 63.6 mol % neopentane and about 13.6 to about 36.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 0.4 to about 0.2 mol % neopentane and about 99.6 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 96.6 mol % neopentane and about 0.2 to about 3.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 80.6 to about 59.6 mol % neopentane and about 19.4 to about 40.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 97.6 mol % neopentane and about 0.2 to about 2.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 74.2 to about 56.0 mol % neopentane and about 25.8 to about 44.0 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 0.2 to about 0.8 mol % neopentane and about 99.2 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 98.2 mol % neopentane and about 0.2 to about 1.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 76.6 to about 50.0 mol % neopentane and about 23.4 to about 50.0 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 1.0 to about 0.2 mol % neopentane and about 99.0 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene;
    • wherein the composition has a boiling point of from about −40° C. to about 120° C. at a pressure of about 1 atm, for example, wherein the composition has a boiling point of from about −40° C. to about 120° C. at a pressure of about 1 atm, for example, about −40° C. to about 100° C., about −40° C. to about 80° C., about −40° C. to about 60° C., about −40° C. to about 40° C., about −40° C. to about 20° C., about −40° C. to about 0° C., about −40° C. to about −20° C., about −20° C. to about 120° C., about −20° C. to about 100° C., about −20° C. to about 80° C., about −20° C. to about 60° C., about −20° C. to about 40° C., about −20° C. to about 20° C., about −20° C. to about 0° C., about 0° C. to about 120° C., about 0° C. to about 100° C., about 0° C. to about 80° C., about 0° C. to about 60° C., about 0° C. to about 40° C., about 0° C. to about 20° C., about 20° C. to about 120° C., about 20° C. to about 100° C., about 20° C. to about 80° C., about 20° C. to about 60° C., about 20° C. to about 40° C., about 40° C. to about 120° C., about 40° C. to about 100° C., about 40° C. to about 80° C., about 40° C. to about 60° C., about 60° C. to about 120° C., about 60° C. to about 100° C., about 60° C. to about 80° C., about 80° C. to about 120° C., about 80° C. to about 100° C., or about 100° C. to about 120° C.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about −40° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about −20° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 0° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 20° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 30° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 40° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 60° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 80° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 100° C. at a pressure of about 1 atm.


In some embodiments, the composition comprising neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene has a boiling point of about 120° C. at a pressure of about 1 atm.


In some embodiments, the compositions provided herein further comprise one or more additional components (i.e., additives). In some embodiments, the one or more additional components are each independently selected from the group consisting of a lubricant, a pour point modifier, an anti-foam agent, a viscosity improver, an emulsifier, a dispersant, an oxidation inhibitor, an extreme pressure agent, a corrosion inhibitor, a detergent, a catalyst, a surfactant, a flame retardant, a preservative, a colorant, an antioxidant, a reinforcing agent, a filler, an antistatic agent, a solubilizing agents, an IR attenuating agent, a nucleating agent, a cell controlling agent, an extrusion aid, a stabilizing agent, a thermally insulating agent, a plasticizer, a viscosity modifier, an impact modifier, a gas barrier resin, a polymer modifier, a rheology modifier, an antibacterial agent, a vapor pressure modifier, a UV absorber, a cross-linking agent, a permeability modifier, a bitterant, a propellant, an acid catcher, or any mixture thereof.


Methods of Use

The inventive compositions can be used in a wide range of applications, including, but not limited to, use as aerosol propellants, refrigerants, and heat transfer media.


Uses as a Heat Transfer Medium

The compositions provided herein can act as a working fluid used to carry heat from a heat source to a heat sink. Such heat transfer compositions may also be useful as a refrigerant in a cycle wherein the fluid undergoes a phase change; that is, from a liquid to a gas and back, or vice versa.


Exemplary heat transfer systems include, but are not limited to, air conditioners, freezers, refrigerators, heat pumps, water chillers, flooded evaporator chillers, direct expansion chillers, walk-in coolers, heat pumps, mobile refrigerators, mobile air conditioning units, and combinations thereof.


In some embodiments, the compositions provided herein may be useful in mobile heat transfer systems, including refrigeration, air conditioning, or heat pump systems or apparatus. In some embodiments, the compositions provided herein may be useful in stationary heat transfer systems, including refrigeration, air conditioning, or heat pump systems or apparatus.


As used herein, the term “mobile heat transfer system” refers to any refrigeration, air conditioner, or heating apparatus incorporated into a transportation unit for the road, rail, sea or air. In addition, mobile refrigeration or air conditioner units include those apparatus that are independent of any moving carrier and are known as “intermodal” systems. Such intermodal systems include “containers’ (combined sea/land transport) as well as “swap bodies” (combined road/rail transport).


As used herein, the term “stationary heat transfer system” refers to a system that is fixed in place during operation. A stationary heat transfer system may be located within or attached to a building, or may be a stand-alone device located out of doors, such as a soft drink vending machine. Such a stationary application may be a stationary air conditioning device or heat pump, including but not limited to, a chiller, a high temperature heat pumps, which may be a trans-critical heat pump (e.g., one that operates with a condenser temperature above 50° C., 70° C., 80° C., 100° C., 120° C., 140° C., 160° C., 180° C., or 200° C.), a residential, commercial or industrial air conditioning system, and may be window-mounted, ductless, ducted, packaged terminal, a chiller, and one that is exterior but connected to a building, such as a rooftop system. In stationary refrigeration applications, the compositions provided herein may be useful in high temperature, medium temperature and/or low temperature refrigeration equipment including commercial, industrial or residential refrigerators and freezers, ice machines, self-contained coolers and freezers, flooded evaporator chillers, direct expansion chillers, walk-in and reach-in coolers and freezers, and combination systems. In some embodiments, the compositions provided herein may be used in supermarket refrigerator systems.


In some embodiments, the compositions provided herein may be useful in methods for producing cooling, producing heating, and transferring heat.


In some embodiments, the present application provides a method for producing cooling, comprising evaporating a composition provided herein in the vicinity of a body to be cooled, and thereafter condensing said composition.


In some embodiments, the present application provides a method for producing heating, comprising condensing a composition provided herein in the vicinity of a body to be heated, and thereafter evaporating said compositions.


In some embodiments, the present application provides a method of using a composition provided herein as a heat transfer fluid composition. In some embodiments, the method comprises transporting said composition from a heat source to a heat sink.


Any of the compositions provided herein may be useful as a replacement for a currently used (“incumbent”) refrigerant, including, but not limited to, R-123 (or HFC-123, 2,2-dichloro-1,1,1-trifluoroethane), R-11 (or CFC-11, trichlorofluoromethane), R-12 (or CFC-12, dichlorodifluoromethane), R-22 (chlorodifluoromethane), R-245fa (or HFC-245fa, 1,1,1,3,3-pentafluoropropane), R-114 (or CFC-114, 1,2-dichloro-1,1,2,2-tetrafluoroethane), R-236fa (or HFC-236fa, 1,1,1,3,3,3-hexafluoropropane), R-236ea (or HFC-236ea, 1,1,1,2,3,3-hexafluoropropane), and R-124 (or HCFC-124, 2-chloro-1,1,1,2-tetrafluoroethane), among others.


As used herein, the term “incumbent refrigerant” refers to the refrigerant for which the heat transfer system was designed to operate, or the refrigerant that is resident in the heat transfer system.


In some embodiments, the present application provides a method for operating a heat transfer system or for transferring heat that is designed to operate with an incumbent refrigerant by charging an empty system with a composition provided herein, or by substantially replacing said incumbent refrigerant with a composition provided herein.


As used herein, the term “substantially replacing” refers to allowing the incumbent refrigerant to drain from the system, or pumping the incumbent refrigerant from the system, and then charging the system with a composition of the present invention (i.e., a composition provided herein). The system may be flushed with one or more quantities of the replacement refrigerant before being charged. It shall be understood that some small quantity of the incumbent refrigerant may be present in the system after the system has been charged with the composition provided herein.


In some embodiments, the present application provides a method for recharging a heat transfer system comprising an incumbent refrigerant and a lubricant, said method comprising substantially removing the incumbent refrigerant from the heat transfer system while retaining a substantial portion of the lubricant in said system and introducing a composition provided herein to the heat transfer system. In some embodiments, the lubricant in the system is partially replaced.


In some embodiments, the compositions provided herein may be used to top-off a refrigerant charge in a chiller. For example, if a chiller using HCFC-123 has diminished performance due to leakage of refrigerant, the compositions provided herein may be added to bring performance back up to specification.


In some embodiments, a heat exchange system comprising a composition of the invention is provided, wherein said system is selected from the group consisting of air conditioners, freezers, refrigerators, heat pumps, water chillers, flooded evaporator chillers, direct expansion chillers, walk-in coolers, heat pumps, mobile refrigerators, mobile air conditioning units, and systems having combinations thereof. In some embodiments, the composition provided herein may be useful in secondary loop systems wherein these compositions serve as the primary refrigerant thus providing cooling to a secondary heat transfer fluid that thereby cools a remote location.


Each of a vapor-compression refrigeration system, an air conditioning system, and a heat pump system includes as components an evaporator, a compressor, a condenser, and an expansion device. A vapor-compression cycle re-uses refrigerant in multiple steps producing a cooling effect in one step and a heating effect in a different step. The cycle can be described simply as follows. Liquid refrigerant enters an evaporator through an expansion device, and the liquid refrigerant boils in the evaporator, by withdrawing heat from the environment, at a low temperature to form a vapor and produce cooling. The low-pressure vapor enters a compressor where the vapor is compressed to raise its pressure and temperature. The higher-pressure (compressed) vapor refrigerant then enters the condenser in which the refrigerant condenses and discharges its heat to the environment. The refrigerant returns to the expansion device through which the liquid expands from the higher-pressure level in the condenser to the low-pressure level in the evaporator, thus repeating the cycle.


In some embodiments, the present application provides a heat transfer system comprising a composition provided herein. In some embodiments, the present application provides a refrigeration, air-conditioning, or heat pump apparatus comprising a composition provided herein. In some embodiments, the present application provides a stationary refrigeration or air-conditioning apparatus comprising a composition provided herein. In some embodiments, the present application provides a mobile refrigeration or air conditioning apparatus comprising a composition provided herein.


Propellants

In some embodiments, the present application provides a composition as described herein for use as a propellant (e.g., in a sprayable composition). In some embodiments, the present application provides a sprayable composition comprising a composition provided herein. In some embodiments, the active ingredient to be sprayed together with inert ingredients, solvents, and other materials may also be present in the sprayable composition. In some embodiments, the sprayable composition is an aerosol. Suitable active materials to be sprayed include, but are not limited to, cosmetic materials, such as deodorants, perfumes, hair sprays, cleaners, and polishing agents, as well as medicinal materials such as anti-asthma and anti-halitosis medications.


In some embodiments, the present application provides a process for producing aerosol products. In some embodiments, the process comprises the step of adding a composition provided herein to one or more active ingredients in an aerosol container, wherein said composition functions as a propellant.


EXAMPLES

The invention will be described in greater detail by way of specific examples. The following examples are offered for illustrative purposes, and are not intended to limit the invention in any manner. Those of skill in the art will readily recognize a variety of non-critical parameters which can be changed or modified to yield essentially the same results.


Example 1. Compositions of E-HFO-1336mzz and Neopentane

The binary system of E-HFO-1336mzz/neopentane was explored for potential azeotropic and near-azeotropic behavior. To determine the relative volatility of this binary system, the PTx method as described herein was used. The pressure in a PTx cell of known volume was measured at constant temperature of 29.88° C. for various binary compositions. The collected experimental data are displayed in Table 1 below, where X2=liquid mole fraction of E-HFO-1336mzz; Y2=vapor mole fraction of E-HFO-1336mzz; Pexp=experimentally measured pressure; and Pcalc=pressure as calculated by NRTL model.













TABLE 1





X2
Y2
psia, expt
psia, calc
(pcalc/pexp)-1



















0
0
28.95




0.00365
0.01299
29.27
29.2493
−7.07E−04 


0.00843
0.02925
29.67
29.6307
−1.32E−03 


0.01809
0.05972
30.41
30.3664
−1.43E−03 


0.06643
0.17653
33.42
33.4348
4.43E−04


0.14533
0.29412
36.81
36.8276
4.79E−04


0.24612
0.38547
39.39
39.3919
4.76E−05


0.34667
0.44894
40.83
40.8352
1.27E−04


0.44829
0.50201
41.62
41.6126
−1.78E−04 


0.56542
0.56068
41.87
41.8789
2.12E−04


0.65475
0.60949
41.63
41.6328
6.73E−05


0.75779
0.67766
40.75
40.7363
−3.36E−04 


0.85193
0.7619
39.11
39.0868
−5.94E−04 


0.9333
0.86793
36.67
36.6737
1.02E−04


0.97972
0.95357
34.66
34.6996
1.14E−03


0.99014
0.97659
34.14
34.1806
1.19E−03


0.99356
0.98453
33.96
34.0032
1.27E−03


1
1
33.66












FIG. 1 displays a plot of the pressure vs composition data over the compositional range of 0-1 liquid mole fraction of E-HFO-1336mzz. The top curve of FIG. 1 represents the bubble point (“BP”) locus, and the bottom curve of FIG. 1 represents the dew point (“DP”) locus. FIG. 1 demonstrates the formation of an azeotrope at 29.88° C., of composition 0.552 mole fraction E-1,1,1,4,4,4-hexafluoro-2-butene and 0.448 mole fraction neopentane, as evidenced by the maximum in the Px diagram at a pressure of 41.8 psia.


Based on these VLE data, interaction coefficients were extracted. The NRTL model was run over the temperature range of −40 to 120° C. in increments of 10° C., allowing pressure to vary such that the azeotropic condition (X2=Y2) was met. The resulting predictions of azeotropes in the E-HFO-1336mzz/neopentane system are displayed in Table 2.














TABLE 2








Azeotrope
E-HFO-1336mzz
Neopentane



Temp
Pressure
Vapor
Vapor



(° C.)
(psi)
Mole Fraction
Mole Fraction





















−40
2.0
0.40865
0.59135



−30
3.5
0.43624
0.56376



−20
5.9
0.46123
0.53877



−10
9.3
0.48380
0.51620



0
14.1
0.50411
0.49589



10
20.9
0.52229
0.47771



20
30.0
0.53845
0.46155



30
41.9
0.55266
0.44734



40
57.4
0.56495
0.43505



50
77.0
0.57528
0.42472



60
101.7
0.58353
0.41647



70
132.5
0.58945
0.41055



80
171.2
0.59246
0.40754



90
220.8
0.59081
0.40919



100
278.1
0.58257
0.41744



110
331.2
0.57921
0.42079



120
389.6
0.57392
0.42608










The NRTL model was used to predict azeotropes over a pressure range of 1-30 atm at 1 atm increments, the results of which are displayed in Table 3.














TABLE 3








Azeotrope
Vapor
Vapor



Pressure
Temperature
Mole Fraction
Mole Fraction



(atm)
(° C.)
E-HFO-1336mzz
Neopentane





















1
0.9
0.5059
0.4941



2
19.4
0.5376
0.4624



3
31.6
0.5547
0.4453



4
40.8
0.5659
0.4341



5
48.4
0.5737
0.4263



6
54.8
0.5795
0.4205



7
60.4
0.5838
0.4162



8
65.4
0.5871
0.4129



9
69.9
0.5894
0.4106



10
74.0
0.5911
0.4089



11
77.7
0.5921
0.4079



12
81.2
0.5926
0.4074



13
84.3
0.5925
0.4075



14
87.2
0.5920
0.4080



15
89.9
0.5908
0.4092



16
92.4
0.5890
0.4110



17
94.6
0.5856
0.4144



18
97.3
0.5834
0.4166



19
100.2
0.5825
0.4175



20
103.1
0.5817
0.4183



21
105.9
0.5808
0.4192



22
108.6
0.5798
0.4202



23
111.2
0.5787
0.4213



24
113.8
0.5775
0.4225



25
116.3
0.5762
0.4238



26
118.8
0.5747
0.4253



27
121.2
0.5731
0.4269



28
123.5
0.5714
0.4286



29
125.8
0.5699
0.4301



30
128.0
0.5684
0.4316










The model was run over a temperature range from −40 to 120° C. in 20° C. increments, and also at 29.88° C. for the purpose of comparison to experimentally measured results. At each temperature, the model was run over the full range from 0 to 1 of E-HFO-1336mzz liquid molar composition in increments of 0.002. Thus the model was run at a total of 5010 combinations of temperature and E-HFO-1336mzz liquid molar composition (10 temperatures×501 compositions=5010 combinations). Table 4 shows representative results in increments of 0.10 E-HFO-1336mzz liquid molar composition, or the boundaries of near-azeotropic behavior.
















TABLE 4






Liquid Mole
Vapor Mole








Fraction
Fraction
Liquid Mole
Vapor Mole
Bubble Point
Dew Point
[(BP-


Temp
E-HFO-
E-HFO-
Fraction
Fraction
Pressure
Pressure
DP)/BP]*


(° C.)
1336mzz
1336mzz
Neopentane
Neopentane
(psia)
(psia)
100%






















−40
0.000
0.0000
1.0000
1.0000
1.6172
1.6172
0.00%


−40
0.002
0.0071
0.9980
0.9929
1.6255
1.6196
0.37%


−40
0.018
0.0573
0.9820
0.9427
1.6864
1.6386
2.84%


−40
0.020
0.0629
0.9800
0.9371
1.6933
1.6409
3.09%


−40
0.038
0.1077
0.9620
0.8923
1.7499
1.6627
4.98%


−40
0.040
0.1121
0.9600
0.8879
1.7555
1.6651
5.15%


−40
0.230
0.3230
0.7700
0.6770
2.0094
1.9074
5.08%


−40
0.232
0.3242
0.7680
0.6758
2.0104
1.9099
5.00%


−40
0.282
0.3517
0.7180
0.6483
2.0309
1.9688
3.05%


−40
0.284
0.3527
0.7160
0.6473
2.0315
1.9710
2.98%


−40
0.300
0.3606
0.7000
0.6394
2.0361
1.9878
2.37%


−40
0.400
0.4050
0.6000
0.5950
2.0494
2.0490
0.02%


−40
0.500
0.4463
0.5000
0.5537
2.0410
2.0020
1.91%


−40
0.502
0.4472
0.4980
0.5528
2.0406
2.0001
1.99%


−40
0.524
0.4564
0.4760
0.5436
2.0359
1.9766
2.91%


−40
0.526
0.4573
0.4740
0.5427
2.0354
1.9743
3.00%


−40
0.528
0.4581
0.4720
0.5419
2.0349
1.9720
3.09%


−40
0.566
0.4747
0.4340
0.5253
2.0239
1.9241
4.93%


−40
0.568
0.4756
0.4320
0.5244
2.0232
1.9214
5.03%


−40
0.976
0.9109
0.0240
0.0891
1.4505
1.3774
5.04%


−40
0.978
0.9174
0.0220
0.0826
1.4429
1.3753
4.69%


−40
0.986
0.9450
0.0140
0.0550
1.4114
1.3667
3.17%


−40
0.988
0.9523
0.0120
0.0477
1.4033
1.3646
2.76%


−40
0.998
0.9916
0.0020
0.0084
1.3608
1.3541
0.50%


−40
1.000
1.0000
0.0000
0.0000
1.3520
1.3520
0.00%


−20
0.000
0.0000
1.0000
1.0000
4.4342
4.4342
0.00%


−20
0.002
0.0073
0.9980
0.9927
4.4582
4.4408
0.39%


−20
0.016
0.0533
0.9840
0.9467
4.6144
4.4873
2.76%


−20
0.018
0.0592
0.9820
0.9408
4.6352
4.4940
3.05%


−20
0.032
0.0973
0.9680
0.9027
4.7707
4.5412
4.81%


−20
0.034
0.1023
0.9660
0.8977
4.7888
4.5481
5.03%


−20
0.282
0.3758
0.7180
0.6242
5.7518
5.4616
5.05%


−20
0.284
0.3769
0.7160
0.6231
5.7544
5.4688
4.96%


−20
0.300
0.3856
0.7000
0.6144
5.7738
5.5252
4.31%


−20
0.332
0.4020
0.6680
0.5980
5.8056
5.6308
3.01%


−20
0.334
0.4030
0.6660
0.5970
5.8073
5.6370
2.93%


−20
0.400
0.4340
0.6000
0.5660
5.8469
5.8021
0.77%


−20
0.500
0.4784
0.5000
0.5216
5.8538
5.8357
0.31%


−20
0.592
0.5209
0.4080
0.4791
5.8059
5.6328
2.98%


−20
0.594
0.5219
0.4060
0.4781
5.8043
5.6267
3.06%


−20
0.600
0.5248
0.4000
0.4752
5.7991
5.6082
3.29%


−20
0.642
0.5464
0.3580
0.4536
5.7551
5.4677
4.99%


−20
0.644
0.5475
0.3560
0.4525
5.7527
5.4607
5.08%


−20
0.964
0.8941
0.0360
0.1059
4.5456
4.3150
5.07%


−20
0.966
0.8991
0.0340
0.1009
4.5285
4.3087
4.85%


−20
0.982
0.9425
0.0180
0.0575
4.3841
4.2584
2.87%


−20
0.998
0.9931
0.0020
0.0069
4.2241
4.2091
0.36%


−20
1.000
1.0000
0.0000
0.0000
4.2030
4.2030
0.00%


0
0.000
0.0000
1.0000
1.0000
10.3222
10.3222
0.00%


0
0.002
0.0073
0.9980
0.9927
10.3796
10.3379
0.40%


0
0.016
0.0539
0.9840
0.9461
10.7565
10.4483
2.86%


0
0.018
0.0600
0.9820
0.9400
10.8070
10.4642
3.17%


0
0.030
0.0937
0.9700
0.9063
11.0938
10.5606
4.81%


0
0.032
0.0989
0.9680
0.9011
11.1391
10.5768
5.05%


0
0.322
0.4155
0.6780
0.5845
13.8866
13.1876
5.03%


0
0.324
0.4166
0.6760
0.5834
13.8927
13.2051
4.95%


0
0.370
0.4405
0.6300
0.5595
14.0094
13.5832
3.04%


0
0.372
0.4415
0.6280
0.5585
14.0136
13.5983
2.96%


0
0.400
0.4552
0.6000
0.5448
14.0645
13.7933
1.93%


0
0.500
0.5022
0.5000
0.4978
14.1454
14.1449
0.00%


0
0.600
0.5508
0.4000
0.4492
14.0751
13.8675
1.47%


0
0.648
0.5764
0.3520
0.4236
13.9817
13.5701
2.94%


0
0.650
0.5775
0.3500
0.4225
13.9768
13.5562
3.01%


0
0.700
0.6073
0.3000
0.3927
13.8276
13.1823
4.67%


0
0.710
0.6137
0.2900
0.3863
13.7907
13.1028
4.99%


0
0.712
0.6150
0.2880
0.3850
13.7830
13.0868
5.05%


0
0.948
0.8743
0.0520
0.1257
11.7385
11.1494
5.02%


0
0.950
0.8782
0.0500
0.1218
11.7061
11.1339
4.89%


0
0.972
0.9259
0.0280
0.0741
11.3228
10.9651
3.16%


0
0.974
0.9306
0.0260
0.0694
11.2854
10.9499
2.97%


0
0.998
0.9941
0.0020
0.0059
10.7988
10.7698
0.27%


0
1.000
1.0000
0.0000
0.0000
10.7549
10.7549
0.00%


20
0.000
0.0000
1.0000
1.0000
21.1399
21.1399
0.00%


20
0.002
0.0073
0.9980
0.9927
21.2595
21.1727
0.41%


20
0.016
0.0537
0.9840
0.9463
22.0503
21.4048
2.93%


20
0.018
0.0598
0.9820
0.9402
22.1570
21.4382
3.24%


20
0.030
0.0938
0.9700
0.9062
22.7665
21.6408
4.94%


20
0.032
0.0990
0.9680
0.9010
22.8632
21.6748
5.20%


20
0.352
0.4450
0.6480
0.5550
29.3816
27.8860
5.09%


20
0.354
0.4461
0.6460
0.5539
29.3947
27.9239
5.00%


20
0.400
0.4701
0.6000
0.5299
29.6494
28.7384
3.07%


20
0.402
0.4711
0.5980
0.5289
29.6586
28.7708
2.99%


20
0.500
0.5195
0.5000
0.4805
29.9403
29.8645
0.25%


20
0.600
0.5700
0.4000
0.4300
29.9002
29.7282
0.58%


20
0.698
0.6265
0.3020
0.3735
29.4990
28.6171
2.99%


20
0.700
0.6278
0.3000
0.3722
29.4863
28.5883
3.05%


20
0.776
0.6821
0.2240
0.3179
28.8389
27.3994
4.99%


20
0.778
0.6838
0.2220
0.3162
28.8169
27.3663
5.03%


20
0.922
0.8431
0.0780
0.1569
26.2733
24.9483
5.04%


20
0.924
0.8462
0.0760
0.1538
26.2206
24.9152
4.98%


20
0.964
0.9172
0.0360
0.0828
25.0275
24.2620
3.06%


20
0.966
0.9213
0.0340
0.0787
24.9602
24.2297
2.93%


20
0.998
0.9948
0.0020
0.0052
23.7709
23.7203
0.21%


20
1.000
1.0000
0.0000
0.0000
23.6889
23.6889
0.00%


29.88
0.000
0.0000
1.0000
1.0000
28.9758
28.9758
0.00%


29.88
0.002
0.0072
0.9980
0.9928
29.1409
29.0215
0.41%


29.88
0.016
0.0534
0.9840
0.9466
30.2362
29.3445
2.95%


29.88
0.018
0.0595
0.9820
0.9405
30.3844
29.3912
3.27%


29.88
0.030
0.0934
0.9700
0.9066
31.2334
29.6733
5.00%


29.88
0.032
0.0986
0.9680
0.9014
31.3685
29.7208
5.25%


29.88
0.366
0.4575
0.6340
0.5425
40.9262
38.8602
5.05%


29.88
0.368
0.4586
0.6320
0.5414
40.9445
38.9135
4.96%


29.88
0.370
0.4597
0.6300
0.5403
40.9626
38.9666
4.87%


29.88
0.372
0.4608
0.6280
0.5392
40.9805
39.0194
4.79%


29.88
0.374
0.4618
0.6260
0.5382
40.9981
39.0720
4.70%


29.88
0.376
0.4629
0.6240
0.5371
41.0155
39.1243
4.61%


29.88
0.378
0.4640
0.6220
0.5360
41.0327
39.1763
4.52%


29.88
0.380
0.4650
0.6200
0.5350
41.0497
39.2280
4.44%


29.88
0.382
0.4661
0.6180
0.5339
41.0664
39.2794
4.35%


29.88
0.384
0.4672
0.6160
0.5328
41.0829
39.3305
4.27%


29.88
0.386
0.4682
0.6140
0.5318
41.0992
39.3814
4.18%


29.88
0.388
0.4693
0.6120
0.5307
41.1152
39.4319
4.09%


29.88
0.390
0.4703
0.6100
0.5297
41.1311
39.4820
4.01%


29.88
0.392
0.4714
0.6080
0.5286
41.1467
39.5319
3.92%


29.88
0.394
0.4724
0.6060
0.5276
41.1621
39.5814
3.84%


29.88
0.396
0.4735
0.6040
0.5265
41.1773
39.6305
3.76%


29.88
0.398
0.4745
0.6020
0.5255
41.1922
39.6793
3.67%


29.88
0.400
0.4756
0.6000
0.5244
41.2070
39.7278
3.59%


29.88
0.414
0.4828
0.5860
0.5172
41.3043
40.0558
3.02%


29.88
0.416
0.4838
0.5840
0.5162
41.3173
40.1010
2.94%


29.88
0.500
0.5260
0.5000
0.4740
41.6894
41.4985
0.46%


29.88
0.600
0.5774
0.4000
0.4226
41.6991
41.5591
0.34%


29.88
0.700
0.6359
0.3000
0.3641
41.1831
40.1523
2.50%


29.88
0.718
0.6478
0.2820
0.3522
41.0224
39.8037
2.97%


29.88
0.720
0.6491
0.2800
0.3509
41.0031
39.7638
3.02%


29.88
0.800
0.7104
0.2000
0.2896
39.9532
38.0322
4.81%


29.88
0.812
0.7211
0.1880
0.2789
39.7420
37.7579
4.99%


29.88
0.814
0.7229
0.1860
0.2771
39.7053
37.7120
5.02%


29.88
0.902
0.8206
0.0980
0.1794
37.5605
35.6725
5.03%


29.88
0.904
0.8233
0.0960
0.1767
37.4977
35.6263
4.99%


29.88
0.960
0.9133
0.0400
0.0867
35.4128
34.3478
3.01%


29.88
0.962
0.9171
0.0380
0.0829
35.3253
34.3028
2.89%


29.88
0.998
0.9951
0.0020
0.0049
33.5673
33.5026
0.19%


29.88
1.000
1.0000
0.0000
0.0000
33.4587
33.4587
0.00%


40
0.000
0.0000
1.0000
1.0000
39.1175
39.1175
0.00%


40
0.002
0.0071
0.9980
0.9929
39.3421
39.1803
0.41%


40
0.016
0.0529
0.9840
0.9471
40.8366
39.6247
2.97%


40
0.018
0.0590
0.9820
0.9410
41.0395
39.6889
3.29%


40
0.028
0.0873
0.9720
0.9127
42.0165
40.0121
4.77%


40
0.030
0.0927
0.9700
0.9073
42.2047
40.0772
5.04%


40
0.378
0.4681
0.6220
0.5319
56.1782
53.3429
5.05%


40
0.380
0.4692
0.6200
0.5308
56.2040
53.4172
4.96%


40
0.400
0.4800
0.6000
0.5200
56.4444
54.1395
4.08%


40
0.426
0.4936
0.5740
0.5064
56.7116
55.0067
3.01%


40
0.428
0.4947
0.5720
0.5053
56.7301
55.0694
2.93%


40
0.500
0.5315
0.5000
0.4685
57.2133
56.8210
0.69%


40
0.600
0.5837
0.4000
0.4163
57.3115
57.2081
0.18%


40
0.700
0.6429
0.3000
0.3571
56.6735
55.4940
2.08%


40
0.736
0.6674
0.2640
0.3326
56.2229
54.5604
2.96%


40
0.738
0.6688
0.2620
0.3312
56.1938
54.5054
3.00%


40
0.740
0.6702
0.2600
0.3298
56.1644
54.4501
3.05%


40
0.800
0.7176
0.2000
0.2824
55.0530
52.6872
4.30%


40
0.900
0.8239
0.1000
0.1761
51.9480
49.5417
4.63%


40
0.954
0.9060
0.0460
0.0940
49.3528
47.8448
3.06%


40
0.956
0.9095
0.0440
0.0905
49.2407
47.7826
2.96%


40
0.998
0.9953
0.0020
0.0047
46.5752
46.4927
0.18%


40
1.000
1.0000
0.0000
0.0000
46.4321
46.4321
0.00%


60
0.000
0.0000
1.0000
1.0000
66.7508
66.7508
0.00%


60
0.002
0.0069
0.9980
0.9931
67.1411
66.8632
0.41%


60
0.016
0.0516
0.9840
0.9484
69.7544
67.6585
3.00%


60
0.018
0.0575
0.9820
0.9425
70.1115
67.7734
3.33%


60
0.028
0.0854
0.9720
0.9146
71.8390
68.3526
4.85%


60
0.030
0.0907
0.9700
0.9093
72.1732
68.4694
5.13%


60
0.398
0.4842
0.6020
0.5158
99.4245
94.3842
5.07%


60
0.400
0.4853
0.6000
0.5147
99.4736
94.5224
4.98%


60
0.444
0.5092
0.5560
0.4908
100.4082
97.3428
3.05%


60
0.446
0.5102
0.5540
0.4898
100.4443
97.4591
2.97%


60
0.500
0.5388
0.5000
0.4612
101.2191
100.0780
1.13%


60
0.600
0.5927
0.4000
0.4073
101.6574
101.6166
0.04%


60
0.700
0.6531
0.3000
0.3469
100.6874
99.1097
1.57%


60
0.764
0.6989
0.2360
0.3011
99.1535
96.1892
2.99%


60
0.766
0.7004
0.2340
0.2996
99.0919
96.0881
3.03%


60
0.800
0.7284
0.2000
0.2716
97.9001
94.3058
3.67%


60
0.946
0.8988
0.0540
0.1012
88.7653
86.0797
3.03%


60
0.948
0.9020
0.0520
0.0980
88.5816
85.9667
2.95%


60
0.998
0.9956
0.0020
0.0044
83.3043
83.1736
0.16%


60
1.000
1.0000
0.0000
0.0000
83.0634
83.0634
0.00%


80
0.000
0.0000
1.0000
1.0000
106.7445
106.7445
0.00%


80
0.002
0.0067
0.9980
0.9933
107.3858
106.9363
0.42%


80
0.014
0.0441
0.9860
0.9559
111.1113
108.0998
2.71%


80
0.016
0.0499
0.9840
0.9501
111.7122
108.2958
3.06%


80
0.028
0.0828
0.9720
0.9172
115.2035
109.4849
4.96%


80
0.030
0.0880
0.9700
0.9120
115.7668
109.6852
5.25%


80
0.416
0.4950
0.5840
0.5050
167.0991
158.5962
5.09%


80
0.418
0.4962
0.5820
0.5038
167.1918
158.8495
4.99%


80
0.460
0.5194
0.5400
0.4806
168.8860
163.7680
3.03%


80
0.462
0.5205
0.5380
0.4795
168.9549
163.9796
2.94%


80
0.500
0.5412
0.5000
0.4588
170.0653
167.5014
1.51%


80
0.600
0.5968
0.4000
0.4032
171.1919
171.1762
0.01%


80
0.700
0.6587
0.3000
0.3413
169.5099
167.0483
1.45%


80
0.768
0.7084
0.2320
0.2916
166.4468
161.4755
2.99%


80
0.770
0.7100
0.2300
0.2900
166.3295
161.2920
3.03%


80
0.800
0.7350
0.2000
0.2650
164.3623
158.4508
3.60%


80
0.900
0.8391
0.1000
0.1609
154.5696
148.3564
4.02%


80
0.944
0.9001
0.0560
0.0999
148.3449
143.8749
3.01%


80
0.946
0.9032
0.0540
0.0968
148.0292
143.6728
2.94%


80
0.998
0.9959
0.0020
0.0041
138.7018
138.4930
0.15%


80
1.000
1.0000
0.0000
0.0000
138.2971
138.2971
0.00%


100
0.000
0.0000
1.0000
1.0000
162.0606
162.0606
0.00%


100
0.002
0.0063
0.9980
0.9937
163.0789
162.3803
0.43%


100
0.014
0.0421
0.9860
0.9579
169.0432
164.3232
2.79%


100
0.016
0.0477
0.9840
0.9523
170.0136
164.6512
3.15%


100
0.026
0.0743
0.9740
0.9257
174.7674
166.3096
4.84%


100
0.028
0.0793
0.9720
0.9207
175.6990
166.6450
5.15%


100
0.400
0.4784
0.6000
0.5216
270.4013
256.5804
5.11%


100
0.402
0.4796
0.5980
0.5204
270.5470
257.2455
4.92%


100
0.438
0.5005
0.5620
0.4995
272.9099
264.6125
3.04%


100
0.440
0.5016
0.5600
0.4984
273.0274
264.9359
2.96%


100
0.500
0.5355
0.5000
0.4645
275.9366
272.8608
1.11%


100
0.600
0.5928
0.4000
0.4072
278.2866
278.3577
−0.03%


100
0.700
0.6566
0.3000
0.3434
277.3187
274.7297
0.93%


100
0.756
0.6978
0.2440
0.3022
274.8945
266.7121
2.98%


100
0.758
0.6994
0.2420
0.3006
274.7739
266.2803
3.09%


100
0.794
0.7295
0.2060
0.2705
271.9438
258.5450
4.93%


100
0.796
0.7312
0.2040
0.2688
271.7221
258.1176
5.01%


100
0.888
0.8269
0.1120
0.1731
251.5621
238.9478
5.01%


100
0.890
0.8293
0.1100
0.1707
251.0532
238.5452
4.98%


100
0.952
0.9148
0.0480
0.0852
233.6140
226.4451
3.07%


100
0.954
0.9180
0.0460
0.0820
232.9938
226.0677
2.97%


100
0.998
0.9960
0.0020
0.0040
218.3357
217.9789
0.16%


100
1.000
1.0000
0.0000
0.0000
217.6210
217.6210
0.00%


120
0.000
0.0000
1.0000
1.0000
236.1168
236.1168
0.00%


120
0.002
0.0060
0.9980
0.9940
237.7196
236.6528
0.45%


120
0.004
0.0118
0.9960
0.9882
239.3178
237.1915
0.89%


120
0.006
0.0175
0.9940
0.9825
240.9116
237.7328
1.32%


120
0.008
0.0232
0.9920
0.9768
242.5012
238.2769
1.74%


120
0.010
0.0288
0.9900
0.9712
244.0867
238.8236
2.16%


120
0.012
0.0342
0.9880
0.9658
245.6682
239.3732
2.56%


120
0.014
0.0396
0.9860
0.9604
247.2460
239.9254
2.96%


120
0.016
0.0449
0.9840
0.9551
248.8201
240.4805
3.35%


120
0.024
0.0651
0.9760
0.9349
255.0835
242.7293
4.84%


120
0.026
0.0700
0.9740
0.9300
256.6420
243.2988
5.20%


120
0.370
0.4533
0.6300
0.5467
374.6714
355.8479
5.02%


120
0.372
0.4545
0.6280
0.5455
374.9127
356.3524
4.95%


120
0.426
0.4874
0.5740
0.5126
380.6432
369.0815
3.04%


120
0.428
0.4886
0.5720
0.5114
380.8278
369.5134
2.97%


120
0.500
0.5307
0.5000
0.4693
386.2785
382.5140
0.97%


120
0.600
0.5896
0.4000
0.4104
390.1957
390.4366
−0.06%


120
0.700
0.6549
0.3000
0.3451
389.6846
386.8445
0.73%


120
0.800
0.7341
0.2000
0.2659
383.6353
375.4644
2.13%


120
0.900
0.8404
0.1000
0.1596
369.4663
359.4971
2.70%


120
0.962
0.9304
0.0380
0.0696
353.7368
343.1236
3.00%


120
0.964
0.9337
0.0360
0.0663
353.0395
342.2334
3.06%


120
0.966
0.9371
0.0340
0.0629
352.3105
341.3537
3.11%


120
0.972
0.9475
0.0280
0.0525
349.7199
338.7722
3.13%


120
0.974
0.9511
0.0260
0.0489
348.1987
337.9295
2.95%


120
0.998
0.9960
0.0020
0.0040
329.1331
328.3877
0.23%


120
1.000
1.0000
0.0000
0.0000
327.6335
327.6335
0.00%









Near-azeotropes formed between E-HFO-1336mzz and neopentane at 1 atm are shown in Table 5. Table 5 shows representative data in increments of 0.10 E-HFO-1336mzz liquid molar composition, or the boundaries of near-azeotropic behavior.

















TABLE 5







Liquid Mole
Vapor Mole









Fraction
Fraction
Liquid Mole
Liquid Mole
Bubble Point
Dew Point
[(BP-


Pressure
Temp
E-HFO-
E-HFO-
Fraction
Fraction
Pressure
Pressure
DP)/BP]*


(atm)
(° C.)
1336mzz
1336mzz
Neopentane
Neopentane
(psia)
(psia)
100%























1.00
9.461
0
0
1
1
14.69595
14.69595
0.00%


1.00
9.305
0.002
0.01
1.00
0.993
14.696
14.636
0.41%


1.00
8.308
0.016
0.05
0.98
0.946
14.696
14.270
2.90%


1.00
8.177
0.018
0.06
0.98
0.940
14.696
14.225
3.21%


1.00
7.449
0.03
0.0938898
0.97
0.9061102
14.69595
13.98093
4.87%


1.00
7.336
0.032
0.0991343
0.968
0.9008656
14.69595
13.94488
5.11%


1.00
1.409
0.324
0.4177095
0.676
0.5822905
14.69595
13.95334
5.05%


1.00
1.195
0.37
0.4414781
0.63
0.5585219
14.69595
14.23698
3.12%


1.00
1.187
0.372
0.4424725
0.628
0.5575275
14.69595
14.24871
3.04%


1.00
1.180
0.374
0.4434643
0.626
0.5565357
14.69595
14.26035
2.96%


1.00
1.094
0.4
0.4561451
0.6
0.5438549
14.69595
14.40299
1.99%


1.00
0.946
0.5
0.5031367
0.5
0.4968633
14.69595
14.695
0.01%


1.00
1.065
0.6
0.5519321
0.4
0.4480679
14.69595
14.48902
1.41%


1.00
1.244
0.652
0.5800897
0.348
0.4199103
14.69595
14.2598
2.97%


1.00
1.252
0.654
0.5812312
0.346
0.4187688
14.69595
14.25034
3.03%


1.00
1.589
0.714
0.6181589
0.286
0.3818411
14.69595
13.96853
4.95%


1.00
1.603
0.716
0.6194943
0.284
0.3805057
14.69595
13.95961
5.01%


1.00
5.262
0.942
0.8666191
0.058
0.1333809
14.69595
13.95456
5.04%


1.00
5.325
0.944
0.8703764
0.056
0.1296236
14.69595
13.97141
4.93%


1.00
6.231
0.97
0.9241145
0.03
0.0758854
14.69595
14.24138
3.09%


1.00
6.308
0.972
0.9286651
0.028
0.0713348
14.69595
14.26647
2.92%


1.00
7.418184
0.998
0.9943818
0.002
0.00561824
14.69595
14.65994
0.25%


1.00
7.512796
1
1
0
0
14.69595
14.69595
0.00%









The detailed data in Tables 4-5 are broadly summarized in Table 6 below. From the results in Table 5, azeotrope-like compositions with differences of 3% or less between bubble point pressures and dew point pressures exist from:

    • (1) 0.002 to 0.016 mole fraction E-1336mzz and from 0.984 to 0.998 mole percent neopentane at 1 atmosphere pressure boiling at from 8.31 to 9.31° C.;
    • (2) 0.374 to 0.652 mole fraction E-1336mzz and from 0.384 to 0.626 mole percent neopentane at 1 atmosphere pressure boiling at from 0.95 to 1.24° C.; and
    • (3) 0.972 to 0.998 mole fraction E-1336mzz and from 0.002 to 0.028 mole percent neopentane at 1 atmosphere pressure boiling at from 6.31 to 7.42° C.


Ranges of 3% azeotrope-like compositions (based on [(BP−VP)/BP]×100≤3) are listed in Table 6.













TABLE 6









E-HFO-1336mzz Vapor




Temp
Mole Percentage Range



Components
(° C.)
(Remainder Neopentane)




















E-HFO-1336mzz/
−40
0.002 to 0.018 and



Neopentane

0.284 to 0.524 and





0.988 to 0.998



E-HFO-1336mzz/
−20
0.002 to 0.016 and



Neopentane

0.334 to 0.592 and





0.982 to 0.998



E-HFO-1336mzz/
0
0.002 to 0.016 and



Neopentane

0.372 to 0.648 and





0.974 to 0.998



E-HFO-1336mzz/
20
0.002 to 0.016 and



Neopentane

0.402 to 0.698 and





0.966 to 0.998



E-HFO-1336mzz/
29.88
0.002 to 0.016 and



Neopentane

0.416 to 0.718 and





0.962 to 0.998



E-HFO-1336mzz/
40
0.002 to 0.016 and



Neopentane

0.428 to 0.736 and





0.956 to 0.998



E-HFO-1336mzz/
60
0.002 to 0.016 and



Neopentane

0.446 to 0.764 and





0.948 to 0.009



E-HFO-1336mzz/
80
0.002 to 0.014 and



Neopentane

0.462 to 0.768 and





0.946 to 0.998



E-HFO-1336mzz/
100
0.002 to 0.014 and



Neopentane

0.440 to 0.756 and





0.954 to 0.998



E-HFO-1336mzz/
120
0.002 to 0.014 and



Neopentane

0.428 to 0.962 and





0.974 to 0.998










Example 2. Compositions of Z-HFO-1336mzz and Neopentane

The binary system of Z-HFO-1336mzz/neopentane was explored for potential azeotropic and near-azeotropic behavior. To determine the relative volatility of this binary system, the PTx method described herein was used. The pressure in a PTx cell of known volume was measured at constant temperature of 29.90° C. for various binary compositions. The collected experimental data are displayed in Table 7 below, where X2=liquid mole fraction of neopentane; Y2=vapor mole fraction of neopentane; Pexp=experimentally measured pressure; and Pcalc=pressure as calculated by NRTL model.













TABLE 7





X2
Y2
psia, expt
psia, calc
(pcalc/pexp)-1



















0
0
12.98




0.00565
0.04447
13.53
13.5319
1.38E−04


0.00915
0.06959
13.88
13.8641
−1.14E−03 


0.0182
0.12772
14.67
14.6968
1.83E−03


0.06537
0.32642
18.45
18.4289
−1.15E−03 


0.14432
0.48593
22.92
22.9065
−5.87E−04 


0.24575
0.58368
26.49
26.5246
1.31E−03


0.34458
0.63707
28.61
28.6679
2.02E−03


0.45163
0.67591
30.22
30.1073
−3.73E−03 


0.55029
0.70455
30.96
30.9557
−1.38E−04 


0.65079
0.73293
31.51
31.5177
2.45E−04


0.75045
0.76664
31.79
31.806 
5.04E−04


0.8517
0.81802
31.66
31.6557
−1.37E−04 


0.93498
0.8925
30.77
30.7664
−1.17E−04 


0.98191
0.96298
29.6
29.6229
7.74E−04


0.99116
0.98103
29.26
29.3112
1.75E−03


0.99555
0.99022
29.1
29.1511
1.76E−03


1
1
28.98











The vapor pressure vs. neopentane liquid mole fraction data shown in Table 7 are plotted in FIG. 2, with the experimental data points shown as solid points. The solid line represents bubble point predictions using the NRTL equation. The dashed line represents predicted dew points. FIG. 2 demonstrates the formation of an azeotrope at 29.90° C. of the composition containing 0.220 mole fraction Z-1,1,1,4,4,4-hexafluoro-2-butene and 0.780 mole fraction neopentane, as evidenced by the maximum in the Px diagram at a pressure of 31.8 psia.


Based on these VLE data, interaction coefficients were extracted. The NRTL model was run over the temperature range of −40 to 120° C. in increments of 10° C. allowing pressure to vary such that the azeotropic condition (X2=Y2) was met. The resulting predicted azeotropes in the Z-HFO-1336mzz/neopentane system, and the experimentally determined data at 29.90° C., are displayed in Table 8.














TABLE 8








Azeotrope
Vapor
Vapor



Temp
Pressure
Mole Fraction
Mole Fraction



(° C.)
(psi)
Z-HFO-1336mzz
Neopentane





















−40
1.6
0.07883
0.92117



−30
2.8
0.09995
0.90005



−20
4.6
0.12089
0.87911



−10
7.2
0.14154
0.85846



0
10.9
0.16187
0.83813



10
16.0
0.18187
0.81813



20
22.9
0.20154
0.79846



30
31.9
0.22092
0.77908



40
43.5
0.24008
0.75992



50
58.3
0.25908
0.74092



60
76.8
0.27803
0.72197



70
99.9
0.29709
0.70291



80
128.6
0.31656
0.68344



90
164.6
0.33709
0.66291



100
211.4
0.36145
0.63855



110
260.8
0.38626
0.61374



120
308.7
0.40156
0.59844










The model was used to predict azeotropes over a pressure range of 1-30 atm at 1 atm increments, the results of which are displayed in Table 9.














TABLE 9








Azeotrope
Vapor
Vapor



Pressure
Temperature
Mole Fraction
Mole Fraction



(atm)
(° C.)
Z-HFO-1336mzz
Neopentane





















1
7.7
0.17728
0.82272



2
27.5
0.21605
0.78395



3
40.4
0.24089
0.75911



4
50.3
0.25963
0.74037



5
58.3
0.27489
0.72511



6
65.2
0.28788
0.71212



7
71.1
0.29927
0.70073



8
76.4
0.30948
0.69052



9
81.1
0.31879
0.68121



10
85.4
0.32741
0.67259



11
89.3
0.33551
0.66449



12
92.8
0.34325
0.65675



13
96.0
0.35079
0.64921



14
98.9
0.35839
0.64161



15
101.6
0.36666
0.63334



16
104.3
0.37595
0.62405



17
107.6
0.38215
0.61785



18
110.8
0.38757
0.61243



19
114.0
0.39255
0.60745



20
117.0
0.39718
0.60282



21
120.0
0.40153
0.59847



22
122.9
0.40563
0.59437



23
125.7
0.40952
0.59048



24
128.4
0.41322
0.58678



25
131.0
0.41674
0.58326



26
133.6
0.42010
0.57990



27
136.1
0.42332
0.57668



28
138.5
0.42640
0.57360



29
140.9
0.42935
0.57065



30
143.2
0.43191
0.56809










The model was run over a temperature range from −40 to 120° C. in 20 deg. increments, and also at 29.90° C. for the purpose of comparison to experimentally measured results. At each temperature, the model was run over the full range from 0 to 1 of Z-HFO-1336mzz liquid molar composition in increments of 0.002. Thus the model was run at a total of 5010 combinations of temperature and Z-HFO-1336mzz liquid molar composition (10 temperatures×501 compositions=5010). Table 10 shows representative results in increments of 0.10 Z-HFO-1336mzz liquid molar composition, or the boundaries of near-azeotropic behavior.
















TABLE 10






Liquid Mole
Vapor Mole







Total
Fraction
Fraction
Liquid Mole
Vapor Mole
Bubble Point
Dew Point
[(BP-


Temp
Z-HFO-
Z-HFO-
Fraction
Fraction
Pressure
Pressure
DP)/BP]*


(° C.)
1336mzz
1336mzz
Neopentane
Neopentane
(psia)
(psia)
100%






















−40
0.000
0.0000
1.0000
1.0000
1.6172
1.6172
0.00%


−40
0.002
0.0031
0.9980
0.9969
1.6190
1.6184
0.04%


−40
0.100
0.0909
0.9000
0.9091
1.6437
1.6413
0.15%


−40
0.148
0.1110
0.8520
0.8890
1.6360
1.5870
2.99%


−40
0.150
0.1117
0.8500
0.8883
1.6356
1.5824
3.25%


−40
0.160
0.1150
0.8400
0.8850
1.6334
1.5550
4.80%


−40
0.162
0.1156
0.8380
0.8844
1.6329
1.5487
5.15%


−40
0.998
0.9546
0.0020
0.0454
0.3663
0.3510
4.18%


−40
1.000
1.0000
0.0000
0.0000
0.3503
0.3503
0.00%


−20
0.000
0.0000
1.0000
1.0000
4.4342
4.4342
0.00%


−20
0.002
0.0035
0.9980
0.9965
4.4412
4.4382
0.07%


−20
0.100
0.1085
0.9000
0.8915
4.5869
4.5823
0.10%


−20
0.192
0.1510
0.8080
0.8490
4.5692
4.4375
2.88%


−20
0.194
0.1516
0.8060
0.8484
4.5682
4.4267
3.10%


−20
0.208
0.1560
0.7920
0.8440
4.5608
4.3389
4.86%


−20
0.210
0.1566
0.7900
0.8434
4.5597
4.3248
5.15%


−20
0.996
0.9387
0.0040
0.0613
1.3342
1.2616
5.44%


−20
0.998
0.9682
0.0020
0.0318
1.2958
1.2592
2.82%


−20
1.000
1.0000
0.0000
0.0000
1.2568
1.2568
0.00%


0
0.000
0.0000
1.0000
1.0000
10.3222
10.3222
0.00%


0
0.002
0.0039
0.9980
0.9961
10.3431
10.3328
0.10%


0
0.100
0.1241
0.9000
0.8759
10.8575
10.7847
0.67%


0
0.200
0.1786
0.8000
0.8214
10.8959
10.8317
0.59%


0
0.238
0.1921
0.7620
0.8079
10.8625
10.5375
2.99%


0
0.240
0.1928
0.7600
0.8072
10.8603
10.5148
3.18%


0
0.256
0.1977
0.7440
0.8023
10.8415
10.3091
4.91%


0
0.258
0.1983
0.7420
0.8017
10.8390
10.2807
5.15%


0
0.994
0.9329
0.0060
0.0671
3.8553
3.6348
5.72%


0
0.996
0.9541
0.0040
0.0459
3.7760
3.6280
3.92%


0
0.998
0.9764
0.0020
0.0236
3.6957
3.6212
2.02%


0
1.000
1.0000
0.0000
0.0000
3.6144
3.6144
0.00%


20
0.000
0.0000
1.0000
1.0000
21.1399
21.1399
0.00%


20
0.002
0.0043
0.9980
0.9957
21.1914
21.1640
0.13%


20
0.100
0.1376
0.9000
0.8624
22.6006
22.2674
1.47%


20
0.200
0.2008
0.8000
0.7992
22.8812
22.8811
0.00%


20
0.282
0.2326
0.7180
0.7674
22.7823
22.1007
2.99%


20
0.284
0.2333
0.7160
0.7667
22.7778
22.0583
3.16%


20
0.302
0.2390
0.6980
0.7610
22.7337
21.6320
4.85%


20
0.304
0.2396
0.6960
0.7604
22.7284
21.5803
5.05%


20
0.992
0.9312
0.0080
0.0688
9.3530
8.8251
5.64%


20
0.994
0.9473
0.0060
0.0527
9.2073
8.8088
4.33%


20
0.996
0.9641
0.0040
0.0359
9.0599
8.7925
2.95%


20
0.998
0.9816
0.0020
0.0184
8.9109
8.7762
1.51%


20
1.000
1.0000
0.0000
0.0000
8.7600
8.7600
0.00%


29.90
0.000
0.0000
1.0000
1.0000
28.9936
28.9936
0.00%


29.90
0.002
0.0044
0.9980
0.9956
29.0702
29.0283
0.14%


29.90
0.100
0.1436
0.9000
0.8564
31.2508
30.6506
1.92%


29.90
0.200
0.2109
0.8000
0.7891
31.7848
31.7473
0.12%


29.90
0.300
0.2514
0.7000
0.7486
31.6654
30.7977
2.74%


29.90
0.302
0.2521
0.6980
0.7479
31.6593
30.7436
2.89%


29.90
0.304
0.2527
0.6960
0.7473
31.6530
30.6882
3.05%


29.90
0.326
0.2599
0.6740
0.7401
31.5767
29.9999
4.99%


29.90
0.328
0.2605
0.6720
0.7395
31.5691
29.9311
5.19%


29.90
0.990
0.9240
0.0100
0.0760
13.8642
13.0165
6.11%


29.90
0.992
0.9380
0.0080
0.0620
13.6749
12.9924
4.99%


29.90
0.994
0.9526
0.0060
0.0474
13.4836
12.9683
3.82%


29.90
0.996
0.9678
0.0040
0.0322
13.2902
12.9444
2.60%


29.90
0.998
0.9836
0.0020
0.0164
13.0946
12.9205
1.33%


29.90
1.000
1.0000
0.0000
0.0000
12.8968
12.8968
0.00%


40
0.000
0.0000
1.0000
1.0000
39.1175
39.1175
0.00%


40
0.002
0.0046
0.9980
0.9954
39.2292
39.1666
0.16%


40
0.100
0.1494
0.9000
0.8506
42.5267
41.5039
2.41%


40
0.200
0.2206
0.8000
0.7794
43.4682
43.2932
0.40%


40
0.300
0.2640
0.7000
0.7360
43.4226
42.8014
1.43%


40
0.324
0.2724
0.6760
0.7276
43.3303
42.0535
2.95%


40
0.326
0.2731
0.6740
0.7269
43.3215
41.9801
3.10%


40
0.348
0.2804
0.6520
0.7196
43.2138
41.0773
4.94%


40
0.350
0.2811
0.6500
0.7189
43.2030
40.9877
5.13%


40
0.990
0.9312
0.0100
0.0688
19.8257
18.7456
5.45%


40
0.992
0.9440
0.0080
0.0560
19.5804
18.7109
4.44%


40
0.994
0.9572
0.0060
0.0428
19.3326
18.6763
3.40%


40
0.996
0.9710
0.0040
0.0290
19.0822
18.6418
2.31%


40
0.998
0.9852
0.0020
0.0148
18.8290
18.6075
1.18%


40
1.000
1.0000
0.0000
0.0000
18.5732
18.5732
0.00%


60
0.000
0.0000
1.0000
1.0000
66.7508
66.7508
0.00%


60
0.002
0.0048
0.9980
0.9952
66.9722
66.8431
0.19%


60
0.050
0.0964
0.9500
0.9036
71.2049
69.0695
3.00%


60
0.052
0.0994
0.9480
0.9006
71.3424
69.1623
3.06%


60
0.100
0.1599
0.9000
0.8401
73.9384
71.3675
3.48%


60
0.134
0.1919
0.8660
0.8081
75.1282
72.8669
3.01%


60
0.136
0.1936
0.8640
0.8064
75.1851
72.9523
2.97%


60
0.200
0.2385
0.8000
0.7615
76.4161
75.3962
1.33%


60
0.300
0.2873
0.7000
0.7127
76.8076
76.6796
0.17%


60
0.364
0.3117
0.6360
0.6883
76.4600
74.2548
2.88%


60
0.366
0.3125
0.6340
0.6875
76.4433
74.1332
3.02%


60
0.390
0.3209
0.6100
0.6791
76.2178
72.5078
4.87%


60
0.392
0.3216
0.6080
0.6784
76.1969
72.3602
5.04%


60
0.988
0.9319
0.0120
0.0681
37.8216
35.8393
5.24%


60
0.990
0.9424
0.0100
0.0576
37.4342
35.7723
4.44%


60
0.992
0.9532
0.0080
0.0468
37.0431
35.7055
3.61%


60
0.994
0.9644
0.0060
0.0356
36.6482
35.6390
2.75%


60
0.998
0.9878
0.0020
0.0122
35.8472
35.5067
0.95%


60
1.000
1.0000
0.0000
0.0000
35.4409
35.4409
0.00%


80
0.000
0.0000
1.0000
1.0000
106.7445
106.7445
0.00%


80
0.002
0.0050
0.9980
0.9950
107.1575
106.9093
0.23%


80
0.034
0.0737
0.9660
0.9263
112.9502
109.5782
2.99%


80
0.036
0.0773
0.9640
0.9227
113.2653
109.7468
3.11%


80
0.100
0.1694
0.9000
0.8306
121.0224
115.2064
4.81%


80
0.192
0.2498
0.8080
0.7502
126.6249
122.7885
3.03%


80
0.194
0.2511
0.8060
0.7489
126.6973
122.9397
2.97%


80
0.200
0.2551
0.8000
0.7449
126.9045
123.3872
2.77%


80
0.300
0.3092
0.7000
0.6908
128.6011
128.4880
0.09%


80
0.404
0.3519
0.5960
0.6481
127.9126
124.1362
2.95%


80
0.406
0.3526
0.5940
0.6474
127.8807
123.9332
3.09%


80
0.430
0.3617
0.5700
0.6383
127.4454
121.2404
4.87%


80
0.432
0.3624
0.5680
0.6376
127.4049
120.9974
5.03%


80
0.986
0.9330
0.0140
0.0670
66.4262
63.0507
5.08%


80
0.988
0.9418
0.0120
0.0582
65.8393
62.9298
4.42%


80
0.992
0.9602
0.0080
0.0398
64.6508
62.6893
3.03%


80
0.994
0.9698
0.0060
0.0302
64.0491
62.5698
2.31%


80
0.998
0.9896
0.0020
0.0104
62.8306
62.3319
0.79%


80
1.000
1.0000
0.0000
0.0000
62.2136
62.2136
0.00%


100
0.000
0.0000
1.0000
1.0000
162.0606
162.0606
0.00%


100
0.002
0.0052
0.9980
0.9948
162.8079
162.3479
0.28%


100
0.024
0.0565
0.9760
0.9435
170.4614
165.5563
2.88%


100
0.026
0.0607
0.9740
0.9393
171.1079
165.8523
3.07%


100
0.050
0.1062
0.9500
0.8938
178.2764
169.4602
4.95%


100
0.052
0.1096
0.9480
0.8904
178.8269
169.7653
5.07%


100
0.100
0.1787
0.9000
0.8213
190.1334
177.2807
6.76%


100
0.200
0.2722
0.8000
0.7278
204.4969
193.6178
5.32%


100
0.208
0.2779
0.7920
0.7221
205.2348
194.9091
5.03%


100
0.210
0.2793
0.7900
0.7207
205.4114
195.2300
4.96%


100
0.256
0.3084
0.7440
0.6916
208.6711
202.2679
3.07%


100
0.258
0.3096
0.7420
0.6904
208.7805
202.5525
2.98%


100
0.300
0.3324
0.7000
0.6676
210.5275
207.8247
1.28%


100
0.400
0.3780
0.6000
0.6220
211.0931
209.6264
0.69%


100
0.440
0.3945
0.5600
0.6055
210.1069
203.9804
2.92%


100
0.442
0.3953
0.5580
0.6047
210.0407
203.6103
3.06%


100
0.984
0.9342
0.0160
0.0658
109.3571
103.8668
5.02%


100
0.986
0.9417
0.0140
0.0583
108.4855
103.6575
4.45%


100
0.990
0.9574
0.0100
0.0426
106.7243
103.2415
3.26%


100
0.992
0.9656
0.0080
0.0344
105.8347
103.0346
2.65%


100
0.998
0.9911
0.0020
0.0089
103.1293
102.4189
0.69%


100
1.000
1.0000
0.0000
0.0000
102.2152
102.2152
0.00%


120
0.000
0.0000
1.0000
1.0000
236.1168
236.1168
0.00%


120
0.002
0.0054
0.9980
0.9946
237.4794
236.6231
0.36%


120
0.018
0.0451
0.9820
0.9549
248.1231
240.7570
2.97%


120
0.020
0.0497
0.9800
0.9503
249.4243
241.2844
3.26%


120
0.032
0.0760
0.9680
0.9240
257.1173
244.4997
4.91%


120
0.034
0.0801
0.9660
0.9199
258.3829
245.0444
5.16%


120
0.100
0.1903
0.9000
0.8097
290.9384
264.6514
9.04%


120
0.160
0.2557
0.8400
0.7443
300.5716
285.3887
5.05%


120
0.162
0.2575
0.8380
0.7425
300.8051
285.8125
4.98%


120
0.200
0.2891
0.8000
0.7109
304.4655
292.5199
3.92%


120
0.232
0.3118
0.7680
0.6882
306.5936
297.3575
3.01%


120
0.234
0.3131
0.7660
0.6869
306.7023
297.6413
2.95%


120
0.300
0.3523
0.7000
0.6477
308.9822
305.5498
1.11%


120
0.400
0.4009
0.6000
0.5991
308.7450
308.7833
−0.01%


120
0.500
0.4448
0.5000
0.5552
305.0445
295.9952
2.97%


120
0.502
0.4457
0.4980
0.5543
304.9360
295.5923
3.06%


120
0.538
0.4618
0.4620
0.5382
302.7328
287.6782
4.97%


120
0.540
0.4627
0.4600
0.5373
302.5961
287.2072
5.09%


120
0.982
0.9354
0.0180
0.0646
171.3352
162.5178
5.15%


120
0.984
0.9420
0.0160
0.0580
170.0262
162.1598
4.63%


120
0.988
0.9556
0.0120
0.0444
167.3917
161.4485
3.55%


120
0.990
0.9627
0.0100
0.0373
166.0660
161.0952
2.99%


120
0.998
0.9922
0.0020
0.0078
160.7064
159.6975
0.63%


120
1.000
1.0000
0.0000
0.0000
159.3520
159.3520
0.00%









Near-azeotropes formed between Z-HFO-1336mzz and neopentane at 1 atm are shown in Table 11. Table 11 shows representative data in increments of 0.10 Z-HFO-1336mzz liquid molar composition, or the boundaries of near-azeotropic behavior.

















TABLE 11







Liquid Mole
Vapor Mole









Fraction
Fraction
Liquid Mole
Vapor Mole
Bubble Point
Dew Point
[(BP-


Pressure
Temp
Z-HFO-
Z-HFO-
Fraction
Fraction
Pressure
Pressure
DP)/BP]*


(atm)
(° C.)
1336mzz
1336mzz
Neopentane
Neopentane
(psia)
(psia)
100%























1.00
9.5
0.0000
0.0000
1.0000
1.0000
14.6960
14.6960
0.00%


1.00
9.4
0.0020
0.0041
0.9980
0.9959
14.6960
14.6793
0.11%


1.00
7.8
0.2540
0.2075
0.7460
0.7925
14.6960
14.2731
2.88%


1.00
7.8
0.2560
0.2082
0.7440
0.7918
14.6960
14.2473
3.05%


1.00
7.9
0.2740
0.2139
0.7260
0.7861
14.6960
13.9822
4.86%


1.00
7.9
0.2760
0.2145
0.7240
0.7855
14.6960
13.9495
5.08%


1.00
31.5
0.9900
0.9252
0.0100
0.0748
14.6960
13.8141
6.00%


1.00
31.9
0.9920
0.9393
0.0080
0.0607
14.6960
13.9794
4.88%


1.00
32.2
0.9940
0.9538
0.0060
0.0462
14.6960
14.1500
3.72%


1.00
32.6
0.9960
0.9687
0.0040
0.0313
14.6960
14.3261
2.52%


1.00
33.0
0.9980
0.9841
0.0020
0.0159
14.6960
14.5080
1.28%


1.00
33.4
1.0000
1.0000
0.0000
0.0000
14.6960
14.6960
0.00%









The data in Table 10-11 are broadly summarized in Table 12 which shows azeotrope-like compositions, based on the equation [(BP−VP)/BP]×100≤3.













TABLE 12









Liquid Mole Percentage




Temp
Range Z-HFO-1336mzz



Components
(° C.)
(Remainder Neopentane)




















Z-HFO-1336mzz/
−40
0.002 to 0.148



Neopentane



Z-HFO-1336mzz/
−20
0.002 to 0.192



Neopentane



Z-HFO-1336mzz/
0
0.002 to 0.238



Neopentane



Z-HFO-1336mzz/
20
0.002 to 0.382 and



Neopentane

0.996 to 0.998



Z-HFO-1336mzz/
29.90
0.002 to 0.302 and



Neopentane

0.996 to 0.998



Z-HFO-1336mzz/
40
0.002 to 0.324 and



Neopentane

0.996 to 0.998



Z-HFO-1336mzz/
60
0.002 to 0.050 and



Neopentane

0.136 to 0.364 and





0.994 to 0.998



Z-HFO-1336mzz/
80
0.002 to 0.034 and



Neopentane

0.194 to 0.404 and





0.994 to 0.998



Z-HFO-1336mzz/
100
0.002 to 0.024 and



Neopentane

0.258 to 0.440 and





0.992 to 0.998



Z-HFO-1336mzz/
120
0.002 to 0.018 and



Neopentane

0.234 to 0.050 and





0.990 to 0.998










Other Embodiments

1. In some embodiments, the present application provides a composition, comprising:

    • i) neopentane; and
    • ii) a compound selected from E-1,1,1,4,4,4-hexafluoro-2-butene and Z-1,1,1,4,4,4-hexafluoro-2-butene,
    • wherein the E-1,1,1,4,4,4-hexafluoro-2-butene or Z-1,1,1,4,4,4-hexafluoro-2-butene is present in the composition in an amount effective to form an azeotrope composition or an azeotrope-like composition with the neopentane.


2. The composition of embodiment 1, wherein the composition comprises neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene, wherein the E-1,1,1,4,4,4-hexafluoro-2-butene is present in the composition in an amount effective to form an azeotrope composition or an azeotrope-like composition with the neopentane.


3. The composition of embodiment 1 or 2, wherein the composition comprises from about 40 to about 60 mol % neopentane and about 60 to about 40 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.


4. The composition of any one of embodiments 1 to 3, which has a boiling point of from about −40° C. to about 120° C. at a pressure of from about 2 psi to about 390 psi.


5. The composition of any one of embodiments 1 to 4, which is an azeotrope composition.


6. The composition of embodiment 1 or 2, wherein the composition comprises from about 40 to about 50 mol % neopentane and about 60 to about 50 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.


7. The composition of any one of embodiments 1, 2, and 6, which has a boiling point of from about 0.9° C. to about 128° C. at a pressure of from about 1 atm to about 30 atm.


8. The composition of any one of embodiments 1 to 7, which is an azeotrope composition.


9. The composition embodiment 1 or 2, wherein the composition comprises from about 98.4 to about 99.8 mol % neopentane and about 1.6 to about 0.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.


10. The composition of any one of embodiments 1, 2, and 9, which has a boiling point of from about 8.3° C. to about 9.3° C. at a pressure of about 1 atm.


11. The composition of embodiment 1 or 2, wherein the composition comprises from about 38.4 to about 62.6 mol % neopentane and about 65.2 to about 37.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.


12. The composition any one of embodiments 1, 2, and 11, which has a boiling point of from about 0.9° C. to about 1.2° C. at a pressure of about 1 atm.


13. The composition of embodiment 1 or 2, wherein the composition comprises from about 0.2 to about 2.8 mol % neopentane and about 99.8 to about 97.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.


14. The composition of any one of embodiments 1, 2, and 13, which has a boiling point of from about 6.3° C. to about 7.4° C. at a pressure of about 1 atm.


15. The composition of embodiment 1 or 2, wherein the composition comprises:

    • from about 99.8 to about 98.2 mol % neopentane and about 0.2 to about 1.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 71.6 to about 47.6 mol % neopentane and about 28.4 to about 52.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 1.2 to about 0.2 mol % neopentane and about 98.8 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 98.4 mol % neopentane and about 0.2 to about 1.6 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 66.6 to about 40.8 mol % neopentane and about 33.4 to about 59.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 1.8 to about 0.2 mol % neopentane and about 98.2 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 62.8 to about 35.2 mol % neopentane and about 37.2 to about 64.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 2.6 to about 0.2 mol % neopentane and about 97.4 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 59.8 to about 30.2 mol % neopentane and about 40.2 to about 69.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 3.4 to about 0.2 mol % neopentane and about 96.6 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 58.4 to about 28.2 mol % neopentane and about 41.6 to about 71.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 3.8 to about 0.2 mol % neopentane and about 96.2 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 57.2 to about 26.4 mol % neopentane and about 42.8 to about 73.6 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 4.4 to about 0.2 mol % neopentane and about 95.6 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 55.4 to about 23.6 mol % neopentane and about 44.6 to about 76.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 5.2 to about 99.1 mol % neopentane and about 94.8 to about 0.9 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 98.6 mol % neopentane and about 0.2 to about 1.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 53.8 to about 23.2 mol % neopentane and about 46.2 to about 76.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 5.4 to about 0.2 mol % neopentane and about 94.6 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 56 to about 24.4 mol % neopentane and about 44.0 to about 75.6 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 4.6 to about 0.2 mol % neopentane and about 95.4 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 57.2 to about 3.8 mol % neopentane and about 42.8 to about 96.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 2.6 to about 0.2 mol % neopentane and about 97.4 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.


16. The composition any one of embodiments 1, 2, and 15, which has a boiling point of from about −20° C. to about 120° C. at a pressure of about 1 atm.


17. The composition of any one of embodiments 1, 2, and 9 to 16, which is an azeotrope-like composition.


18. The composition of embodiment 1, wherein the composition comprises neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene, wherein the Z-1,1,1,4,4,4-hexafluoro-2-butene is present in the composition in an amount effective to form an azeotrope composition or an azeotrope-like composition with the neopentane.


19. The composition of embodiment 1 or 18, wherein the composition comprises from about 60 to about 93 mol % neopentane and about 40 to about 7 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene.


20. The composition of any one of embodiments 1, 18, and 19, which has a boiling point of from about −40° C. to about 120° C. at a pressure of from about 1.5 psi to about 310 psi.


21. The composition of embodiment 1 or 18, wherein the composition comprises from about 56 to about 83 mol % neopentane and about 44 to about 17 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene.


22. The composition of any one of embodiments 1, 18, and 21, which has a boiling point of from about 5° C. to about 145° C. at a pressure of from about 1 atm to about 30 atm.


23. The composition of any one of embodiments 1 and 18 to 21, which is an azeotrope composition.


24. The composition of embodiment 1 or 18, wherein the composition comprises from about 99.6 to about 79.2 mol % neopentane and about 0.4 to about 20.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene.


25. The composition of any one of embodiments 1, 18, and 24, which has a boiling point of from about 7.8° C. to about 9.4° C. at a pressure of about 1 atm.


26. The composition of embodiment 1 or 18, wherein the composition comprises from about 3.2 to about 1.6 mol % neopentane and about 96.8 to about 98.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene.


27. The composition of any one of embodiments 1, 18, and 26, which has a boiling point of from about 32.6° C. to about 33.0° C. at a pressure of about 1 atm.


28. The composition of embodiment 1 or 18, wherein the composition comprises:

    • from about 99.8 to about 85.2 mol % neopentane and about 0.2 to about 14.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 80.8 mol % neopentane and about 0.2 to about 19.2 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 76.2 mol % neopentane and about 0.2 to about 23.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 61.8 mol % neopentane and about 0.2 to about 38.2 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 0.4 to about 0.2 mol % neopentane and about 99.6 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 69.8 mol % neopentane and about 0.2 to about 30.2 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 67.6 mol % neopentane and about 0.2 to about 32.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 95.0 mol % neopentane and about 0.2 to about 5 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 86.4 to about 63.6 mol % neopentane and about 13.6 to about 36.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 0.4 to about 0.2 mol % neopentane and about 99.6 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 96.6 mol % neopentane and about 0.2 to about 3.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 80.6 to about 59.6 mol % neopentane and about 19.4 to about 40.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 97.6 mol % neopentane and about 0.2 to about 2.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 74.2 to about 56.0 mol % neopentane and about 25.8 to about 44.0 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 0.2 to about 0.8 mol % neopentane and about 99.2 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 99.8 to about 98.2 mol % neopentane and about 0.2 to about 1.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 76.6 to about 50.0 mol % neopentane and about 23.4 to about 50.0 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; or
    • from about 1.0 to about 0.2 mol % neopentane and about 99.0 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene.


29. The composition of any one of embodiments 1, 18, and 28, which has a boiling point of from about −20° C. to about 120° C. at a pressure of about 1 atm.


30. The composition of any one of embodiments 1, 18, and 24 to 29, which is an azeotrope-like composition.


It is to be understood that while the invention has been described in conjunction with the detailed description thereof, the foregoing description is intended to illustrate and not limit the scope of the invention, which is defined by the scope of the appended claims. Other aspects, advantages, and modifications are within the scope of the following claims. It should be appreciated by those persons having ordinary skill in the art(s) to which the present invention relates that any of the features described herein in respect of any particular aspect and/or embodiment of the present invention can be combined with one or more of any of the other features of any other aspects and/or embodiments of the present invention described herein, with modifications as appropriate to ensure compatibility of the combinations. Such combinations are considered to be part of the present invention contemplated by this disclosure.

Claims
  • 1. A composition, comprising: i) neopentane; andii) a compound selected from E-1,1,1,4,4,4-hexafluoro-2-butene and Z-1,1,1,4,4,4-hexafluoro-2-butene,wherein the E-1,1,1,4,4,4-hexafluoro-2-butene or Z-1,1,1,4,4,4-hexafluoro-2-butene is present in the composition in an amount effective to form an azeotrope composition or an azeotrope-like composition with the neopentane.
  • 2. The composition of claim 1, wherein the composition comprises neopentane and E-1,1,1,4,4,4-hexafluoro-2-butene, wherein the E-1,1,1,4,4,4-hexafluoro-2-butene is present in the composition in an amount effective to form an azeotrope composition or an azeotrope-like composition with the neopentane.
  • 3. The composition of claim 2, wherein the composition comprises an azeotrope of from about 40 to about 60 mol % neopentane and about 60 to about 40 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.
  • 4. The composition of claim 3, which has a boiling point of from about −40° C. to about 120° C. at a pressure of from about 2 psi to about 390 psi.
  • 5. (canceled)
  • 6. (canceled)
  • 7. (canceled)
  • 8. (canceled)
  • 9. The composition of claim 2, wherein the composition comprises an azeotrope-like composition of from about 98.4 to about 99.8 mol % neopentane and about 1.6 to about 0.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.
  • 10. The composition of claim 9, which has a boiling point of from about 8.3° C. to about 9.3° C. at a pressure of about 1 atm.
  • 11. (canceled)
  • 12. The composition of claim 2, wherein the composition comprises an azeotrope-like composition of from about 38.4 to about 62.6 mol % neopentane and about 65.2 to about 37.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.
  • 13. (canceled)
  • 14. (canceled)
  • 15. (canceled)
  • 16. (canceled)
  • 17. (canceled)
  • 18. The composition of claim 2, wherein the composition comprises an azeotrope-like composition of: from about 99.8 to about 98.2 mol % neopentane and about 0.2 to about 1.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 71.6 to about 47.6 mol % neopentane and about 28.4 to about 52.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 1.2 to about 0.2 mol % neopentane and about 98.8 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 99.8 to about 98.4 mol % neopentane and about 0.2 to about 1.6 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 66.6 to about 40.8 mol % neopentane and about 33.4 to about 59.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 1.8 to about 0.2 mol % neopentane and about 98.2 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 62.8 to about 35.2 mol % neopentane and about 37.2 to about 64.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 2.6 to about 0.2 mol % neopentane and about 97.4 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 59.8 to about 30.2 mol % neopentane and about 40.2 to about 69.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 3.4 to about 0.2 mol % neopentane and about 96.6 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 58.4 to about 28.2 mol % neopentane and about 41.6 to about 71.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 3.8 to about 0.2 mol % neopentane and about 96.2 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 57.2 to about 26.4 mol % neopentane and about 42.8 to about 73.6 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 4.4 to about 0.2 mol % neopentane and about 95.6 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 55.4 to about 23.6 mol % neopentane and about 44.6 to about 76.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 5.2 to about 99.1 mol % neopentane and about 94.8 to about 0.9 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 99.8 to about 98.6 mol % neopentane and about 0.2 to about 1.4 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 53.8 to about 23.2 mol % neopentane and about 46.2 to about 76.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 5.4 to about 0.2 mol % neopentane and about 94.6 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 56 to about 24.4 mol % neopentane and about 44.0 to about 75.6 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 4.6 to about 0.2 mol % neopentane and about 95.4 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 57.2 to about 3.8 mol % neopentane and about 42.8 to about 96.2 mol % E-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 2.6 to about 0.2 mol % neopentane and about 97.4 to about 99.8 mol % E-1,1,1,4,4,4-hexafluoro-2-butene.
  • 19. The composition of claim 18, which has a boiling point of from about −20° C. to about 120° C. at a pressure of about 1 atm.
  • 20. (canceled)
  • 21. The composition of claim 1, wherein the composition comprises neopentane and Z-1,1,1,4,4,4-hexafluoro-2-butene, wherein the Z-1,1,1,4,4,4-hexafluoro-2-butene is present in the composition in an amount effective to form an azeotrope composition or an azeotrope-like composition with the neopentane.
  • 22. The composition of claim 21, wherein the composition comprises an azeotrope of from about 60 to about 93 mol % neopentane and about 40 to about 7 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene.
  • 23. The composition of claim 22, which has a boiling point of from about −40° C. to about 120° C. at a pressure of from about 1.5 psi to about 310 psi.
  • 24. (canceled)
  • 25. (canceled)
  • 26. (canceled)
  • 27. (canceled)
  • 28. The composition of claim 21, wherein the composition comprises an azeotrope-like composition of from about 99.6 to about 79.2 mol % neopentane and about 0.4 to about 20.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene.
  • 29. The composition of claim 28, which has a boiling point of from about 7.8° C. to about 9.4° C. at a pressure of about 1 atm.
  • 30. (canceled)
  • 31. The composition of claim 21, wherein the composition comprises an azeotrope-like composition of from about 3.2 to about 1.6 mol % neopentane and about 96.8 to about 98.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene.
  • 32. The composition of claim 31, which has a boiling point of from about 32.6° C. to about 33.0° C. at a pressure of about 1 atm.
  • 33. (canceled)
  • 34. The composition of claim 21, wherein the composition comprises an azeotrope of: from about 99.8 to about 85.2 mol % neopentane and about 0.2 to about 14.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 99.8 to about 80.8 mol % neopentane and about 0.2 to about 19.2 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 99.8 to about 76.2 mol % neopentane and about 0.2 to about 23.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 99.8 to about 61.8 mol % neopentane and about 0.2 to about 38.2 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 0.4 to about 0.2 mol % neopentane and about 99.6 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 99.8 to about 69.8 mol % neopentane and about 0.2 to about 30.2 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 99.8 to about 67.6 mol % neopentane and about 0.2 to about 32.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 99.8 to about 95.0 mol % neopentane and about 0.2 to about 5 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 86.4 to about 63.6 mol % neopentane and about 13.6 to about 36.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 0.4 to about 0.2 mol % neopentane and about 99.6 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 99.8 to about 96.6 mol % neopentane and about 0.2 to about 3.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 80.6 to about 59.6 mol % neopentane and about 19.4 to about 40.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 99.8 to about 97.6 mol % neopentane and about 0.2 to about 2.4 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 74.2 to about 56.0 mol % neopentane and about 25.8 to about 44.0 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 0.2 to about 0.8 mol % neopentane and about 99.2 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 99.8 to about 98.2 mol % neopentane and about 0.2 to about 1.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 76.6 to about 50.0 mol % neopentane and about 23.4 to about 50.0 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene; orfrom about 1.0 to about 0.2 mol % neopentane and about 99.0 to about 99.8 mol % Z-1,1,1,4,4,4-hexafluoro-2-butene.
  • 35. The composition of claim 34, which has a boiling point of from about −20° C. to about 120° C. at a pressure of about 1 atm.
  • 36. (canceled)
PCT Information
Filing Document Filing Date Country Kind
PCT/US2020/054689 10/8/2020 WO
Provisional Applications (1)
Number Date Country
62913319 Oct 2019 US