WO2013126253A1 - Azeotropic compositions of 1,1,3,3-tetrachloro-1-fluoropropane and hydrogen fluoride - Google Patents

Azeotropic compositions of 1,1,3,3-tetrachloro-1-fluoropropane and hydrogen fluoride Download PDF

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Publication number
WO2013126253A1
WO2013126253A1 PCT/US2013/025854 US2013025854W WO2013126253A1 WO 2013126253 A1 WO2013126253 A1 WO 2013126253A1 US 2013025854 W US2013025854 W US 2013025854W WO 2013126253 A1 WO2013126253 A1 WO 2013126253A1
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WO
WIPO (PCT)
Prior art keywords
composition
weight percent
hcfc
azeotrope
fluoropropane
Prior art date
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Ceased
Application number
PCT/US2013/025854
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English (en)
French (fr)
Inventor
Daniel C. Merkel
Konstantin A. Pokrovski
Hang T. Pham
Hsueh Sung Tung
Ryan Hulse
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Honeywell International Inc
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Honeywell International Inc
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Publication date
Application filed by Honeywell International Inc filed Critical Honeywell International Inc
Priority to CN201380010342.5A priority Critical patent/CN104114663B/zh
Priority to ES13752004T priority patent/ES2763360T3/es
Priority to EP13752004.5A priority patent/EP2817380B1/en
Priority to JP2014558765A priority patent/JP6219316B2/ja
Priority to MX2014009995A priority patent/MX349583B/es
Priority to IN6717DEN2014 priority patent/IN2014DN06717A/en
Publication of WO2013126253A1 publication Critical patent/WO2013126253A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C19/00Acyclic saturated compounds containing halogen atoms
    • C07C19/08Acyclic saturated compounds containing halogen atoms containing fluorine
    • C07C19/10Acyclic saturated compounds containing halogen atoms containing fluorine and chlorine
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere
    • C09K3/30Materials not provided for elsewhere for aerosols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/50Solvents
    • C11D7/5036Azeotropic mixtures containing halogenated solvents
    • C11D7/504Azeotropic mixtures containing halogenated solvents all solvents being halogenated hydrocarbons
    • C11D7/5045Mixtures of (hydro)chlorofluorocarbons
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/02Materials undergoing a change of physical state when used
    • C09K5/04Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
    • C09K5/041Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems
    • C09K5/044Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds

Definitions

  • the present invention pertains to azeotropic or azeotrope-like compositions of 1,1,3,3-tetrachloro-l-fluoropropane (HCFC-241fa or 241fa) and hydrogen fluoride (HF).
  • HCFC-241fa or 241fa 1,1,3,3-tetrachloro-l-fluoropropane
  • HF hydrogen fluoride
  • Chlorofluorocarbon (CFC) based chemicals have been widely use in industry in a variety of different applications including as refrigerants, aerosol propellants, blowing agents and solvents, among others.
  • CFCs are suspected of depleting the Earth's ozone layer.
  • more environmentally friendly substitutes have been introduced as replacements for CFCs.
  • 1,1,1,3,3-pentafluoropropane (HFC-245fa) is recognized as having favorable physical properties for certain industrial applications, such as foam blowing agents and solvents, and therefore is consider to be a good substitute for the CFCs previously used for these applications.
  • HFC-245fa 1,1,1,3,3-pentafluoropropane
  • the use of certain hydro fluorocarbons, including HFC-245fa in industrial applications is now believed to contribute to the global warming. Accordingly, more environmentally friendly substitutes for hydrofluorocarbons are now being sought.
  • the compound l-chloro-3,3,3-trifluoropropene also known as HCFO-1233zd or simply 1233zd, is a candidate for replacing HFC-245fa in some applications, including uses as blowing agents and solvents.
  • 1233zd has a Z-isomer and an E- isomer. Due to differences in the physical properties between these two isomers, pure 1233zd (E), pure 1233zd (Z), or certain mixtures of the two isomers may be suitable for particular applications as refrigerants, propellants, blowing agents, solvents, or for other uses.
  • 1,1,3,3-Tetrachloro-l-fluoropropane (HCFC-241fa) is a reactant used in the production of both 245fa and 1233zd. See for example U.S. Patent Nos. 5,763,706 and 6,844,475. See also, U.S. Patent Publication No. 2011-0201853 which is directed to an integrated process and methods of producing 1233zd (E).
  • HCFC-241fa 1,1,3,3-tetrachloro-l- fluoropropane
  • HF hydrogen fluoride
  • the present invention is directed to azeotropic or azeotrope-like mixtures of 1,1,3,3-tetrachloro-l-fluoropropane (HCFC-241fa) and hydrogen fluoride.
  • HCFC-241fa 1,1,3,3-tetrachloro-l-fluoropropane
  • hydrogen fluoride hydrogen fluoride
  • the composition comprises effective amounts of 1,1,3,3-tetrachloro-l-fluoropropane (HCFC-241fa) and hydrogen fluoride.
  • the composition comprises from about 99 to about 1 weight percent HF.
  • the composition comprises from about 70 weight percent to about 99 weight percent HF.
  • the composition comprises from about 70 weight percent to about 99 weight percent HF.
  • the composition comprises from about 1 to about 99 weight percent HCFC-241fa.
  • the composition comprises from about 70 weight percent to about 1 weight percent HCFC-241fa.
  • the composition comprises from about 30 weight percent to about 1 weight percent HCFC-241fa.
  • the composition has a boiling point of about from 21°C to about 60°C at a pressure from about 16.5 psia to about 54.6 psia.
  • a heterogeneous azeotropic composition consisting essentially of 1,1,3, 3-tetrachloro-l-fluoropropane (HCFC-241fa) and hydrogen fluoride (HF).
  • the composition consists essentially of from about 90 to about 99 weight percent hydrogen fluoride and from about 10 to about 1 weight percent 1,1,3,3-tetrachloro-l-fluoropropane (HCFC-241fa), which composition has a boiling point of about 30°C to about 60°C at pressure of about 21.4 psia to pressure of about 53.9 psia.
  • Another aspect of the present invention is directed to a method of forming a heterogeneous azeotropic or azeotrope-like composition
  • a method of forming a heterogeneous azeotropic or azeotrope-like composition comprising the step of blending components which consist essentially of from about 1 to about 99 weight percent hydrogen fluoride and from about 99 to about 1 weight percent 1,1,3,3-tetrachloro-l- fluoropropane (HCFC-241fa), which composition has a boiling point of about from 21°C to about 60°C at pressure of about from 16.5 psia to about 54.6 psia.
  • the composition consists of hydrogen fluoride and 1,1,3,3-tetrachloro-l-fluoropropane (HCFC-241fa).
  • the composition comprises from about 99 to about 1 weight percent HF.
  • the composition comprises from about 70 weight percent to about 99 weight percent HF.
  • the composition comprises from about 70 weight percent to about 99 weight percent HF.
  • the composition comprises from about 1 to about 99 weight percent HCFC-241fa.
  • the composition comprises from about 70 weight percent to about 1 weight percent HCFC-241 fa ⁇ in certain embodiments of this method, the composition comprises from about 30 weight percent to about 1 weight percent HCFC-241fa.
  • the composition has a boiling point of about from 21°C to about 60°C at a pressure from about 16.5 psia to about 54.6 psia.
  • the composition consists of about 98 + 2 weight percent HF and about 2 + 2 weight percent HCFC-241fa, and has a boiling point of about 21°C at 16.5 psia.
  • Another aspect of the present invention is directed to a method of separating 241 fa from the azeotropic like mixture of 241 fa and HF comprising the step of extracting the HF from the mixture.
  • the extraction of HF is accomplished using water or other aqueous solution.
  • the extraction of HF is accomplished using sulfuric acid.
  • the extraction of HF is accomplished by distillation.
  • the distillation comprises extractive distillation.
  • the distillation comprises pressure swing distillation.
  • Figure 1 shows a plot of the vapor pressures of the mixtures formed in Example 1 as measured at 30°C and 60°C.
  • HCFC-241fa 1 ,1,3,3-tetrachloro-l-fluoropropane (HCFC-241fa) and HF were fed to a reactor, it was found that the HCFC-241fa forms an azeotropic or azeotrope-like mixture with HF. The unreacted HCFC-241fa/HF intermediate was found in the product stream.
  • thermodynamic state of a fluid is defined by its pressure, temperature, liquid composition and vapor composition.
  • the liquid composition and vapor phase are essentially equal at a given temperature and pressure. In practical terms this means that the components cannot be separated during a phase change.
  • an azeotrope is a liquid mixture that exhibits a maximum or minimum boiling point relative to the boiling points of surrounding mixture compositions.
  • An azeotrope or an azeotrope-like composition is an admixture of two or more different components which, when in liquid form under given pressure, will boil at a substantially constant temperature, which temperature may be higher or lower than the boiling temperatures of the components and which will provide a vapor composition essentially identical to the liquid composition undergoing boiling.
  • azeotropic compositions are defined to include azeotrope-like compositions, which means a composition that behaves like an azeotrope, i.e., has constant-boiling characteristics or a tendency not to fractionate upon boiling or evaporation.
  • azeotrope-like compositions which means a composition that behaves like an azeotrope, i.e., has constant-boiling characteristics or a tendency not to fractionate upon boiling or evaporation.
  • the composition of the vapor formed during boiling or evaporation is the same as or substantially the same as the original liquid composition.
  • the liquid composition if it changes at all, changes only to a minimal or negligible extent. This is in contrast with non-azeotrope-like compositions in which during boiling or evaporation, the liquid composition changes to a substantial degree.
  • the essential features of an azeotrope or an azeotrope-like composition are that at a given pressure, the boiling point of the liquid composition is fixed and that the composition of the vapor above the boiling composition is essentially that of the boiling liquid composition, i.e., essentially no fractionation of the components of the liquid composition takes place. Both the boiling point and the weight percentages of each component of the azeotropic composition may change when the azeotrope or azeotrope-like liquid composition is subjected to boiling at different pressures.
  • an azeotrope or an azeotrope-like composition may be defined in terms of the relationship that exists between its components or in terms of the compositional ranges of the components or in terms of exact weight percentages of each component of the composition characterized by a fixed boiling point at a specified pressure.
  • the present invention provides a composition which comprises effective amounts of hydrogen fluoride and HCFC-241fa to form an azeotropic or azeotrope-like composition.
  • effective amount is meant an amount of each component which, when combined with the other component, results in the formation of an azeotrope or azeotrope-like mixture.
  • inventive compositions preferably are binary azeotropes which consist essentially of combinations of only hydrogen fluoride with HCFC-241 fa ⁇ in the preferred embodiment, the inventive composition contains from about 99 to about 1 weight percent HF, preferably from about 70 weight percent to about 99 weight percent and most preferably from about 70 weight percent to about 99 weight percent.
  • the inventive composition contains from about 1 to about 99 weight percent HCFC-241fa preferably from about 70 weight percent to about 1 weight percent and most preferably from about 30 weight percent to about 1 weight percent.
  • the composition of the present invention has a boiling point of about from 21°C to about 60°C at a pressure from about 16.5 psia to about 54.6 psia.
  • An azeotropic or azeotrope- like composition having about 98 + 2 weight percent HF and about 2 + 2 weight percent HCFC-241fa has been found to boil at about 21°C and 16.5 psia.
  • Binary compositions containing solely 1,1,3,3-tetrachloro-l-fluoropropane (HCFC-241fa) and HF are blended to form a heterogeneous azeotrope mixtures at different compositions.
  • the vapor pressures of the mixtures are measured at about 29.9°C and 60°C and the following results are noticed.
  • Table 1 shows the vapor pressure measurement of HCFC-241fa and HF as a function of composition of weight percent HF at constant temperatures of about 29.9°C and 60°C.
  • Table 1 P-T-X of HCFC-241fa/HF System
  • the azeotropic composition of the HCFC-241fa/HF mixture is also verified by Vapor-Liquid -Liquid Equilibrium (VLLE) experiment. 57.5 g of 1,1,3,3-tetrachloro-l- fluoropropane (HCFC-241fa) are dissolved in 32.5 g of HF to form a heterogeneous mixture (visual observation) at 21°C. The vapor compositions of the mixture were sampled at room temperature of 21°C. The result shows that the azeotropic composition is about 98 ⁇ 2 wt% HF at 21°C.
  • VLLE Vapor-Liquid -Liquid Equilibrium

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Dispersion Chemistry (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Detergent Compositions (AREA)
PCT/US2013/025854 2012-02-23 2013-02-13 Azeotropic compositions of 1,1,3,3-tetrachloro-1-fluoropropane and hydrogen fluoride Ceased WO2013126253A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
CN201380010342.5A CN104114663B (zh) 2012-02-23 2013-02-13 1,1,3,3‑四氯‑1‑氟丙烷与氟化氢的共沸组合物
ES13752004T ES2763360T3 (es) 2012-02-23 2013-02-13 Composiciones azeótropas de 1,1,3,3-tetracloro-1-fluoropropano y fluoruro de hidrógeno
EP13752004.5A EP2817380B1 (en) 2012-02-23 2013-02-13 Azeotropic compositions of 1,1,3,3-tetrachloro-1-fluoropropane and hydrogen fluoride
JP2014558765A JP6219316B2 (ja) 2012-02-23 2013-02-13 1,1,3,3−テトラクロロ−1−フルオロプロパンとフッ化水素の共沸組成物
MX2014009995A MX349583B (es) 2012-02-23 2013-02-13 Composiciones azeotrópicas de 1, 1, 3, 3 - tetracloro - 1 - fluoropropano y fluoruro de hidrógeno.
IN6717DEN2014 IN2014DN06717A (enExample) 2012-02-23 2013-02-13

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US13/403,011 US8519200B1 (en) 2012-02-23 2012-02-23 Azeotropic compositions of 1,1,3,3-tetrachloro-1-fluoropropane and hydrogen fluoride
US13/403,011 2012-02-23

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WO2013126253A1 true WO2013126253A1 (en) 2013-08-29

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US (1) US8519200B1 (enExample)
EP (1) EP2817380B1 (enExample)
JP (1) JP6219316B2 (enExample)
CN (1) CN104114663B (enExample)
ES (1) ES2763360T3 (enExample)
IN (1) IN2014DN06717A (enExample)
MX (1) MX349583B (enExample)
WO (1) WO2013126253A1 (enExample)

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Publication number Priority date Publication date Assignee Title
JP2018135320A (ja) * 2017-01-06 2018-08-30 ハネウェル・インターナショナル・インコーポレーテッドHoneywell International Inc. (e)−1−クロロ−3,3,3−トリフルオロプロペン、hf、及び重質有機化合物、並びに反応器パージを分離するためのシステム及び方法
JP2019531376A (ja) * 2016-08-31 2019-10-31 ハネウェル・インターナショナル・インコーポレーテッドHoneywell International Inc. 1,3,3−トリクロロ−3−フルオロ−1−エン(HCFO−1231zd)及びフッ化水素(HF)の共沸又は共沸様組成物

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US9764998B2 (en) * 2015-05-12 2017-09-19 Honeywell International Inc. Process for making HCFO-1233zd
US10029964B2 (en) 2016-08-30 2018-07-24 Honeywell International Inc. Azeotropic or azeotrope-like compositions of 3,3,3-trifluoropropyne and water
US9950973B2 (en) 2016-08-31 2018-04-24 Honeywell International Inc. Azeotropic or azeotrope-like compositions of 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd) and hydrogen fluoride (HF)

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Publication number Priority date Publication date Assignee Title
JP2019531376A (ja) * 2016-08-31 2019-10-31 ハネウェル・インターナショナル・インコーポレーテッドHoneywell International Inc. 1,3,3−トリクロロ−3−フルオロ−1−エン(HCFO−1231zd)及びフッ化水素(HF)の共沸又は共沸様組成物
JP2018135320A (ja) * 2017-01-06 2018-08-30 ハネウェル・インターナショナル・インコーポレーテッドHoneywell International Inc. (e)−1−クロロ−3,3,3−トリフルオロプロペン、hf、及び重質有機化合物、並びに反応器パージを分離するためのシステム及び方法

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EP2817380A1 (en) 2014-12-31
EP2817380A4 (en) 2015-10-07
MX349583B (es) 2017-08-04
IN2014DN06717A (enExample) 2015-05-22
ES2763360T3 (es) 2020-05-28
US20130221273A1 (en) 2013-08-29
US8519200B1 (en) 2013-08-27
CN104114663A (zh) 2014-10-22
CN104114663B (zh) 2017-04-26
EP2817380B1 (en) 2019-11-27
JP6219316B2 (ja) 2017-10-25
JP2015511243A (ja) 2015-04-16
MX2014009995A (es) 2014-09-12

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