JP6330027B2 - Hf及び2,3,3,3−テトラフルオロプロペンを含む組成物 - Google Patents
Hf及び2,3,3,3−テトラフルオロプロペンを含む組成物 Download PDFInfo
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- JP6330027B2 JP6330027B2 JP2016503696A JP2016503696A JP6330027B2 JP 6330027 B2 JP6330027 B2 JP 6330027B2 JP 2016503696 A JP2016503696 A JP 2016503696A JP 2016503696 A JP2016503696 A JP 2016503696A JP 6330027 B2 JP6330027 B2 JP 6330027B2
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- hfo
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- hydrogen fluoride
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B7/00—Halogens; Halogen acids
- C01B7/19—Fluorine; Hydrogen fluoride
- C01B7/191—Hydrogen fluoride
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C19/00—Acyclic saturated compounds containing halogen atoms
- C07C19/08—Acyclic saturated compounds containing halogen atoms containing fluorine
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C21/00—Acyclic unsaturated compounds containing halogen atoms
- C07C21/02—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds
- C07C21/18—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds containing fluorine
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
− HF:フッ化水素
− HCC−40:クロロメタン、又はCH3Cl
− HCFC−115:クロロペンタフルオロエタン、又はC2F5Cl
− HCFC−124:クロロテトラフルオロエタン、又はC2HF4Cl
− HFC−125:ペンタフルオロエタン、又はC2HF5
− HCFC−133a:1−クロロ−2,2,2−トリフルオロエタン、又はC2H2F3Cl
− HFC−134a:1,1,1,2−テトラフルオロエタン、又はC2H2F4
− HCFC−142b:1−クロロ−1,1−ジフルオロエタン、又はC2H3F2Cl
− HFC−143a:1,1,1−トリフルオロエタン、又はC2H3F3
− HFC−152a:1,1−ジフルオロエタン、又はC2H4F2
− HFO−1132:1,2−ジフルオロエチレン、又はC2H2F2
− HFO−1141:フルオロエチレン、又はC2H3F
− HFO−1234yf:2,3,3,3−テトラフルオロプロペン、又はCH2=CF−CF3
− HFC−245cb:1,1,1,2,2−ペンタフルオロプロパン、又はCF3−CF2−CH3
− HFO−1234zeE:E−1,3,3,3−テトラフルオロプロペン、又はE−CF3−CH=CHF
− HFO−1234zeZ:Z−1,3,3,3−テトラフルオロプロペン、又はZ−CF3−CH=CHF
− HFO−1243zf:3,3,3−トリフルオロプロペン、又はCF3−CH=CH2
− HCFO−1233xf:3,3,3−トリフルオロ−2−クロロプロペン、又はCF3−CCl=CH2
− HCFO−1233zdE:E−3,3,3−トリフルオロ−1−クロロプロペン、又はE−CF3−CH=CHCl
− HCFO−1233zdZ:Z−3,3,3−トリフルオロ−1−クロロプロペン、又はZ−CF3−CH=CHCl
− HFO−1225yeZ:Z−1,1,1,2,3−ペンタフルオロプロペン、又はZ−CHF=CF−CF3
− HFO−1225yeE:E−1,1,1,2,3−ペンタフルオロプロペン、又はE−CHF=CF−CF3
− HFO−1225zc:1,1,3,3,3−ペンタフルオロプロペン、又はCF2=CH−CF3
− HFO−1225yc:1,1,2,3,3−ペンタフルオロプロペン、又はCF2=CF−CF2
− HCFC−1214:ジクロロテトラフルオロプロペン、又はC3F4Cl2
− HCFO−1215:クロロペンタフルオロプロペン、又はC3F5Cl
− HFO−1216:ヘキサフルオロプロペン、又はC3F6
− HCFO−1223:ジクロロトリフルオロプロペン、又はC3HF3Cl2
− HCFO−1224:クロロテトラフルオロプロペン、又はC3HF4Cl
− HCFO−1232:ジクロロジフルオロプロペン、又はC3H2F2Cl2
− HCFO−1233xc:1,1,3−トリフルオロ−2−クロロプロペン、又はCH2F−CCl=CF2
− HCFO−1233xe:1,3,3−トリフルオロ−2−クロロプロペン、又はCHF2−CCl=CHF
− HCFO−1233yb:1,2,3−トリフルオロ−1−クロロプロペン、又はCH2F−CF=CFCl
− HCFO−1233yc:1,1,2−トリフルオロ−3−クロロプロペン、又はCH2Cl−CF=CF2
− HCFO−1233yd:2,3,3−トリフルオロ−1−クロロプロペン、又はCHF2−CF=CHCl
− HCFO−1233ye:1,2,3−トリフルオロ−3−クロロプロペン、又はCHClF−CF=CHF
− HCFO−1233yf:2,3,3−トリフルオロ−3−クロロプロペン、又はCClF2−CF=CH2
− HCFO−1233zb:1,3,3−トリフルオロ−1−クロロプロペン、又はCHF2−CH=CFCl
− HCFO−1233zc:1,1,3−トリフルオロ−3−クロロプロペン、又はCHClF−CH=CF2
− HCFO−1233ze:1,3,3−トリフルオロ−3−クロロプロペン、又はCClF2−CH=CHF
− HFO−1234yc:1,1,2,3−テトラフルオロプロペン、又はCF2=CF−CH2F
− HFO−1234ye:1,2,3,3−テトラフルオロプロペン、又はCHF=CF−CHF2
− HFO−1234zc:1,1,3,3−テトラフルオロプロペン、又はCF2=CH−CHF2
− HCFO−1242:クロロジフルオロプロペン、又はC3H3F2Cl
− HFO−1243yc:1,1,2−トリフルオロプロペン、又はCH3−CF=CF2
− HFO−1243ye:1,2,3−トリフルオロプロペン、又はCH2F−CF=CHF
− HFO−1243yf:2,3,3−トリフルオロプロペン、又はCHF2−CF=CH2
− HFO−1243zc:1,1,3−トリフルオロプロペン、又はCH2F−CH=CF2
− HFO−1243ze:1,3,3−トリフルオロプロペン、又はCHF2−CH=CHF
− HCFO−1251:クロロフルオロプロペン、又はC3H4FCl
− HFO−1252:ジフルオロプロペン、又はC3H4F2
− HFO−216:ヘキサフルオロプロペン、又はC3F6Cl2
− HCFO−217:クロロヘプタフルオロプロパン、又はC3F7Cl
− HFC−218:オクタフルオロプロパン、又はC3F8
− HCFC−225:ジクロロペンタフルオロプロパン、又はC3HF5Cl2
− HCFC−226:クロロヘキサフルオロプロパン、又はC3HF6Cl
− HFC−227:ヘプタフルオロプロパン、又はC3HF7
− HCFC−234:ジクロロテトラフルオロプロパン、又はC3H2F4Cl2
− HCFC−235:クロロペンタフルオロプロパン、又はC3H2F5Cl
− HFC−236:ヘキサフルオロプロパン、又はC3H2F6
− HCFC−243:ジクロロトリフルオロプロパン、又はC3H3F3Cl2
− HCFC−244:クロロテトラフルオロプロパン、又はC3H3F4Cl
− HCFC−244bb:2−クロロ−1,1,1,2−テトラフルオロプロパン、又はCF3−CFCl−CH3
− HFC−245fa:1,1,1,3,3−ペンタフルオロプロパン、又はCF3−CH2−CHF2
− HFC−245ea:1,1,2,3,3−ペンタフルオロプロパン、又はCHF2−CHF−CHF2
− HFC−245eb:1,1,1,2,3−ペンタフルオロプロパン、又はCF3−CHF−CH2F
− HFC−245ca:1,1,2,2,3−ペンタフルオロプロパン、又はCHF2−CF2−CH2F
− HCFC−253:クロロトリフルオロプロパン、又はC3H4F3Cl
− HFC−254:テトラフルオロプロパン、又はC3H4F4
− HCFC−262:クロロジフルオロプロパン、又はC3H5F2Cl
− HFC−263:トリフルオロプロパン、又はC3H5F3
− トリフルオロプロピン:CF3−C≡CH
ロペン、2−クロロ−3−フルオロプロペン、3−クロロ−2−フルオロプロペン、3−クロロ−1−フルオロプロペン、3−クロロ−3−フルオロプロペン、ジフルオロプロペン、1,2−ジフルオロプロペン、2,3−ジフルオロプロペン、1,1−ジフルオロプロペン、1,3−ジフルオロプロペン、3,3−ジフルオロプロペン、1,1,1,2,2−ペンタフルオロプロパン、E−1,3,3,3−テトラフルオロプロペン、Z−1,3,3,3−テトラフルオロプロペン、3,3,3−トリフルオロプロペン、3,3,3−トリフルオロ−2−クロロプロペン、E−3,3,3−トリフルオロ−1−クロロプロペン、Z−3,3,3−トリフルオロ−1−クロロプロペン及びトリフルオロプロピンから選択され得る。
Claims (13)
- フッ化水素と、2,3,3,3−テトラフルオロプロペンと、3,3,3−トリフルオロ−2−クロロプロペンと、任意選択的にE−3,3,3−トリフルオロ−1−クロロプロペンとを含む、共沸又は共沸様組成物。
- フッ化水素、2,3,3,3−テトラフルオロプロペン、3,3,3−トリフルオロ−2−クロロプロペン、並びに、1,1,1,2,2−ペンタフルオロプロパン、E−1,3,3,3−テトラフルオロプロペン、Z−1,3,3,3−テトラフルオロプロペン、3,3,3−トリフルオロプロペン、E−3,3,3−トリフルオロ−1−クロロプロペン、1,1,1,3,3−ペンタフルオロプロパン、2−クロロ−1,1,1,2−テトラフルオロプロパン、トリフルオロプロピン、Z−1,1,1,2,3−ペンタフルオロプロペン及び1,1,1,3,3−ペンタフルオロプロペンから選択される一又は複数の有機化合物を含むことを特徴とする、請求項1に記載の組成物。
- フッ化水素、2,3,3,3−テトラフルオロプロペン、3,3,3−トリフルオロ−2−クロロプロペン、並びに、1,1,1,2,2−ペンタフルオロプロパン、E−1,3,3,3−テトラフルオロプロペン、Z−1,3,3,3−テトラフルオロプロペン、3,3,3−トリフルオロプロペン、E−3,3,3−トリフルオロ−1−クロロプロペン、1,1,1,3,3−ペンタフルオロプロパン、2−クロロ−1,1,1,2−テトラフルオロプロパン、トリフルオロプロピン、Z−1,1,1,2,3−ペンタフルオロプロペン及び1,1,1,3,3−ペンタフルオロプロペンから選択される一又は複数の有機化合物を含むことを特徴とする、請求項1又は2に記載の組成物。
- フッ化水素、2,3,3,3−テトラフルオロプロペン、3,3,3−トリフルオロ−2−クロロプロペン、並びに、1,1,1,2,2−ペンタフルオロプロパン、E−1,3,3,3−テトラフルオロプロペン、Z−1,3,3,3−テトラフルオロプロペン、3,3,3−トリフルオロプロペン及びE−3,3,3−トリフルオロ−1−クロロプロペンから選択される一又は複数の有機化合物を含むことを特徴とする、請求項1から3の何れか一項に記載の組成物。
- 不均一共沸又は不均一共沸様であることを特徴とする、請求項1から4の何れか一項に記載の組成物。
- フッ化水素と、2,3,3,3−テトラフルオロプロペンと、3,3,3−トリフルオロ−2−クロロプロペンと、1,1,1,2,2−ペンタフルオロプロパンと、任意選択的に、E−1,3,3,3−テトラフルオロプロペン、Z−1,3,3,3−テトラフルオロプロペン、3,3,3−トリフルオロプロペン、E−3,3,3−トリフルオロ−1−クロロプロペン、1,1,1,3,3−ペンタフルオロプロパン、2−クロロ−1,1,1,2−テトラフルオロプロパン、トリフルオロプロピン、Z−1,1,1,2,3−ペンタフルオロプロペン及び1,1,1,3,3−ペンタフルオロプロペンから選択される少なくとも一の化合物とを含むことを特徴とする、請求項1から5の何れか一項に記載の組成物。
- フッ化水素と、2,3,3,3−テトラフルオロプロペンと、3,3,3−トリフルオロ−2−クロロプロペンと、E−1,3,3,3−テトラフルオロプロペンと、任意選択的に、Z−1,3,3,3−テトラフルオロプロペン、3,3,3−トリフルオロプロペン、E−3,3,3−トリフルオロ−1−クロロプロペン、1,1,1,3,3−ペンタフルオロプロパン、2−クロロ−1,1,1,2−テトラフルオロプロパン、トリフルオロプロピン、Z−1,1,1,2,3−ペンタフルオロプロペン及び1,1,1,3,3−ペンタフルオロプロペンから選択される少なくとも一の化合物とを含むことを特徴とする、請求項1から6の何れか一項に記載の組成物。
- フッ化水素と、2,3,3,3−テトラフルオロプロペンと、3,3,3−トリフルオロ−2−クロロプロペンと、Z−1,3,3,3−テトラフルオロプロペンと、任意選択的に、3,3,3−トリフルオロプロペン、1,1,1,3,3−ペンタフルオロプロパン及びE−3,3,3−トリフルオロ−1−クロロプロペンから選択される少なくとも一の化合物とを含むことを特徴とする、請求項1から7の何れか一項に記載の組成物。
- フッ化水素と、2,3,3,3−テトラフルオロプロペンと、3,3,3−トリフルオロ−2−クロロプロペンと、3,3,3−トリフルオロプロペンと、任意選択的に、E−3,3,3−トリフルオロ−1−クロロプロペンとを含むことを特徴とする、請求項1から8の何れか一項に記載の組成物。
- フッ化水素、2,3,3,3−テトラフルオロプロペン、3,3,3−トリフルオロ−2−クロロプロペン及びE−3,3,3−トリフルオロ−1−クロロプロペンを含むことを特徴とする、請求項1から9の何れか一項に記載の組成物。
- 1から85重量%のフッ化水素及び合計99から15重量%の有機化合物を含む、請求項1から10の何れか一項に記載の組成物。
- 5から80重量%のフッ化水素及び合計95から20重量%の有機化合物を含む、請求項1から11の何れか一項に記載の組成物。
- 前記組成物の沸点が、0.1から44barの絶対圧で−20℃から80℃、優先的には0.7から18barの絶対圧、有利には0.9から12.5barの絶対圧で、優先的には0℃から40℃である、請求項1から12の何れか一項に記載の組成物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1352482 | 2013-03-20 | ||
FR1352482A FR3003565B1 (fr) | 2013-03-20 | 2013-03-20 | Composition comprenant hf et 2,3,3,3-tetrafluoropropene |
PCT/FR2014/050357 WO2014147310A1 (fr) | 2013-03-20 | 2014-02-21 | Composition comprenant hf et 2,3,3,3-tetrafluoropropene |
Related Child Applications (1)
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JP2018082042A Division JP2018150313A (ja) | 2013-03-20 | 2018-04-23 | Hf及び2,3,3,3−テトラフルオロプロペンを含む組成物 |
Publications (2)
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JP2016514721A JP2016514721A (ja) | 2016-05-23 |
JP6330027B2 true JP6330027B2 (ja) | 2018-05-23 |
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JP2016503696A Active JP6330027B2 (ja) | 2013-03-20 | 2014-02-21 | Hf及び2,3,3,3−テトラフルオロプロペンを含む組成物 |
JP2018082042A Ceased JP2018150313A (ja) | 2013-03-20 | 2018-04-23 | Hf及び2,3,3,3−テトラフルオロプロペンを含む組成物 |
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JP2018082042A Ceased JP2018150313A (ja) | 2013-03-20 | 2018-04-23 | Hf及び2,3,3,3−テトラフルオロプロペンを含む組成物 |
Country Status (7)
Country | Link |
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US (1) | US10252913B2 (ja) |
EP (1) | EP2976317B1 (ja) |
JP (2) | JP6330027B2 (ja) |
CN (2) | CN112374963A (ja) |
ES (1) | ES2872933T3 (ja) |
FR (1) | FR3003565B1 (ja) |
WO (1) | WO2014147310A1 (ja) |
Families Citing this family (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2936806B1 (fr) | 2008-10-08 | 2012-08-31 | Arkema France | Fluide refrigerant |
FR2937328B1 (fr) | 2008-10-16 | 2010-11-12 | Arkema France | Procede de transfert de chaleur |
US20170080773A1 (en) | 2008-11-03 | 2017-03-23 | Arkema France | Vehicle Heating and/or Air Conditioning Method |
FR2950065B1 (fr) | 2009-09-11 | 2012-02-03 | Arkema France | Fluide refrigerant binaire |
FR2950071B1 (fr) | 2009-09-11 | 2012-02-03 | Arkema France | Compositions ternaires pour refrigeration basse capacite |
FR2950069B1 (fr) | 2009-09-11 | 2011-11-25 | Arkema France | Utilisation de compositions ternaires |
FR2950068B1 (fr) | 2009-09-11 | 2012-05-18 | Arkema France | Procede de transfert de chaleur |
FR2950066B1 (fr) | 2009-09-11 | 2011-10-28 | Arkema France | Refrigeration basse et moyenne temperature |
US10035938B2 (en) | 2009-09-11 | 2018-07-31 | Arkema France | Heat transfer fluid replacing R-134a |
FR2962442B1 (fr) | 2010-07-09 | 2016-02-26 | Arkema France | Composition stable de 2,3,3,3-tetrafluoropropene |
FR2964975B1 (fr) | 2010-09-20 | 2012-08-24 | Arkema France | Composition a base de 2,3,3,3-tetrafluoropropene |
FR2974812B1 (fr) | 2011-05-04 | 2014-08-08 | Arkema France | Compositions de transfert de chaleur presentant une miscibilite amelioree avec l'huile de lubrification |
FR2986236B1 (fr) | 2012-01-26 | 2014-01-10 | Arkema France | Compositions de transfert de chaleur presentant une miscibilite amelioree avec l'huile de lubrification |
FR3000093B1 (fr) | 2012-12-26 | 2015-07-17 | Arkema France | Composition azeotropique ou quasi-azeotropique de chloromethane |
FR3000096B1 (fr) | 2012-12-26 | 2015-02-20 | Arkema France | Composition comprenant du 2,3,3,3-tetrafluoropropene |
FR3000095B1 (fr) | 2012-12-26 | 2015-02-20 | Arkema France | Composition comprenant du 2,3,3,3-tetrafluoropropene et du 1,2-difluoroethylene |
FR3003565B1 (fr) * | 2013-03-20 | 2018-06-29 | Arkema France | Composition comprenant hf et 2,3,3,3-tetrafluoropropene |
FR3003567B1 (fr) | 2013-03-20 | 2015-03-06 | Arkema France | Composition comprenant hf et 3,3,3-trifluoropropene |
FR3003566B1 (fr) | 2013-03-20 | 2018-07-06 | Arkema France | Composition comprenant hf et e-3,3,3-trifluoro-1-chloropropene |
FR3003568B1 (fr) | 2013-03-20 | 2018-06-29 | Arkema France | Composition comprenant hf et 3,3,3-trifluoro-2-chloropropene |
FR3003569B1 (fr) | 2013-03-20 | 2015-12-25 | Arkema France | Composition comprenant hf et 1,3,3,3-tetrafluoropropene |
FR3008419B1 (fr) | 2013-07-11 | 2015-07-17 | Arkema France | Compositions a base de 2,3,3,3-tetrafluoropropene presentant une miscibilite amelioree |
FR3015478B1 (fr) | 2013-12-19 | 2015-12-25 | Arkema France | Compositions azeotropiques a base de fluorure d'hydrogene et de z-3,3,3-trifluoro-1-chloropropene |
FR3033791B1 (fr) | 2015-03-18 | 2017-04-14 | Arkema France | Stabilisation du 1-chloro-3,3,3-trifluoropropene |
CN107635955A (zh) | 2015-05-21 | 2018-01-26 | 科慕埃弗西有限公司 | 通过SbF5进行的1233xf至244bb的氢氟化 |
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US10252913B2 (en) | 2019-04-09 |
FR3003565A1 (fr) | 2014-09-26 |
EP2976317A1 (fr) | 2016-01-27 |
JP2018150313A (ja) | 2018-09-27 |
EP2976317B1 (fr) | 2021-03-24 |
CN112374963A (zh) | 2021-02-19 |
JP2016514721A (ja) | 2016-05-23 |
CN105143156A (zh) | 2015-12-09 |
ES2872933T3 (es) | 2021-11-03 |
FR3003565B1 (fr) | 2018-06-29 |
US20160009555A1 (en) | 2016-01-14 |
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