JP5530929B2 - E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンの共沸および共沸混合物様組成物 - Google Patents
E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンの共沸および共沸混合物様組成物 Download PDFInfo
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Description
本出願は、2007年9月6日出願の米国仮特許出願第60/970393号明細書、2007年9月11日出願の米国仮特許出願第60/993254号明細書および米国仮特許出願第60/993240号明細書、2007年12月11日出願の米国仮特許出願第61/012846号明細書および米国特許出願第61/012848号明細書、2008年1月15日出願の米国仮特許出願第61/021132号明細書、米国仮特許出願第61/021139号明細書および米国仮特許出願第61/021145号明細書の優先権を主張するものである。
Claims (24)
- (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)ギ酸メチルと
を含む組成物であって、前記ギ酸メチルが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)ギ酸メチルと
を含む組成物であって、前記ギ酸メチルが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸混合物様組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)n−ペンタンと
を含む組成物であって、前記n−ペンタンが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)n−ペンタンと
を含む組成物であって、前記n−ペンタンが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸混合物様組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)2−メチルブタンと
を含む組成物であって、前記2−メチルブタンが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)2−メチルブタンと
を含む組成物であって、前記2−メチルブタンが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸混合物様組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)1,1,1,3,3−ペンタフルオロブタンと
を含む組成物であって、前記1,1,1,3,3−ペンタフルオロブタンが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)1,1,1,3,3−ペンタフルオロブタンと
を含む組成物であって、前記1,1,1,3,3−ペンタフルオロブタンが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸混合物様組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)トランス−1,2−ジクロロエチレンと
を含む組成物であって、前記トランス−1,2−ジクロロエチレンが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)トランス−1,2−ジクロロエチレンと
を含む組成物であって、前記トランス−1,2−ジクロロエチレンが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸混合物様組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)1,1,1,3,3−ペンタフルオロプロパンと
を含む組成物であって、前記1,1,1,3,3−ペンタフルオロプロパンが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸混合物様組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)ジメトキシメタンと
を含む組成物であって、前記ジメトキシメタンが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸混合物様組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)シクロペンタンと
を含む組成物であって、前記シクロペンタンが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)シクロペンタンと
を含む組成物であって、前記シクロペンタンが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸混合物様組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと
を含む組成物であって、前記Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸組み合わせを形成するのに有効な量で存在する組成物。 - (a)E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと;
(b)Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと
を含む組成物であって、前記Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンが前記E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと共沸混合物様組み合わせを形成するのに有効な量で存在する組成物。 - 共沸もしくは共沸混合物様組成物を発泡剤として使用する工程を含む熱可塑性または熱硬化性発泡体の製造方法であって、前記共沸もしくは共沸混合物様組成物が、E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと、ギ酸メチル、n−ペンタン、2−メチルブタン、1,1,1,3,3−ペンタフルオロブタン、トランス−1,2−ジクロロエチレン、1,1,1,3,3−ペンタフルオロプロパン、ジメトキシメタン、シクロペンタンおよびZ−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンからなる群から選択される成分とを含む方法。
- 共沸もしくは共沸混合物様組成物を凝縮させる工程と、その後冷却されるべき本体の近くで前記共沸もしくは共沸混合物様組成物を蒸発させる工程とを含む冷却を行うための方法であって、前記共沸もしくは共沸混合物様組成物が、E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと、ギ酸メチル、n−ペンタン、2−メチルブタン、1,1,1,3,3−ペンタフルオロブタン、トランス−1,2−ジクロロエチレン、1,1,1,3,3−ペンタフルオロプロパン、ジメトキシメタン、シクロペンタンおよびZ−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンからなる群から選択される成分とを含む方法。
- 共沸もしくは共沸混合物様組成物を溶媒として使用する工程を含む方法であって、前記共沸もしくは共沸混合物様組成物が、E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと、ギ酸メチル、n−ペンタン、2−メチルブタン、1,1,1,3,3−ペンタフルオロブタン、トランス−1,2−ジクロロエチレン、1,1,1,3,3−ペンタフルオロプロパン、ジメトキシメタン、シクロペンタンおよびZ−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンからなる群から選択される成分とを含む方法。
- 共沸もしくは共沸混合物様組成物を噴射剤として使用する工程を含むエアゾール製品の製造方法であって、前記共沸もしくは共沸混合物様組成物が、E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと、ギ酸メチル、n−ペンタン、2−メチルブタン、1,1,1,3,3−ペンタフルオロブタン、トランス−1,2−ジクロロエチレン、1,1,1,3,3−ペンタフルオロプロパン、ジメトキシメタン、シクロペンタンおよびZ−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンからなる群から選択される成分とを含む方法。
- 共沸もしくは共沸混合物様組成物を熱媒として使用する工程を含む方法であって、前記共沸もしくは共沸混合物様組成物が、E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと、ギ酸メチル、n−ペンタン、2−メチルブタン、1,1,1,3,3−ペンタフルオロブタン、トランス−1,2−ジクロロエチレン、1,1,1,3,3−ペンタフルオロプロパン、ジメトキシメタン、シクロペンタンおよびZ−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンからなる群から選択される成分とを含む方法。
- 共沸もしくは共沸混合物様組成物を消火剤または鎮火剤として使用する工程を含む消火または鎮火方法であって、前記共沸もしくは共沸混合物様組成物が、E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと、ギ酸メチル、n−ペンタン、2−メチルブタン、1,1,1,3,3−ペンタフルオロブタン、トランス−1,2−ジクロロエチレン、1,1,1,3,3−ペンタフルオロプロパン、ジメトキシメタン、シクロペンタンおよびZ−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンからなる群から選択される成分とを含む方法。
- 共沸もしくは共沸混合物様組成物を誘電体として使用する工程を含む方法であって、前記共沸もしくは共沸混合物様組成物が、E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと、ギ酸メチル、n−ペンタン、2−メチルブタン、1,1,1,3,3−ペンタフルオロブタン、トランス−1,2−ジクロロエチレン、1,1,1,3,3−ペンタフルオロプロパン、ジメトキシメタン、シクロペンタンおよびZ−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンからなる群から選択される成分とを含む方法。
- 2つ以上の化合物の混合物からの化合物の分離のために共沸もしくは共沸混合物様組成物を使用する工程を含む方法であって、前記共沸もしくは共沸混合物様組成物が、E−1,1,1,4,4,5,5,5−オクタフルオロ−2−ペンテンと、ギ酸メチル、n−ペンタン、2−メチルブタン、1,1,1,3,3−ペンタフルオロブタン、トランス−1,2−ジクロロエチレン、1,1,1,3,3−ペンタフルオロプロパン、ジメトキシメタン、シクロペンタンおよびZ−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンからなる群から選択される成分とを含む方法。
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US97039307P | 2007-09-06 | 2007-09-06 | |
US60/970,393 | 2007-09-06 | ||
PCT/US2008/075345 WO2009032983A1 (en) | 2007-09-06 | 2008-09-05 | Azeotropic and azeotrope-like compositions of e-1,1,1,4,4,5,5,5-octafluoro-2-pentene |
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US (1) | US8632703B2 (ja) |
EP (1) | EP2188348B1 (ja) |
JP (1) | JP5530929B2 (ja) |
KR (1) | KR101527244B1 (ja) |
CN (1) | CN101815773B (ja) |
AR (1) | AR068235A1 (ja) |
AU (1) | AU2008296223B2 (ja) |
BR (1) | BRPI0815462A2 (ja) |
CA (2) | CA2921867A1 (ja) |
ES (1) | ES2560454T3 (ja) |
MX (1) | MX2010002471A (ja) |
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-
2008
- 2008-09-05 KR KR1020107007393A patent/KR101527244B1/ko not_active IP Right Cessation
- 2008-09-05 BR BRPI0815462-7A2A patent/BRPI0815462A2/pt not_active IP Right Cessation
- 2008-09-05 ES ES08829661.1T patent/ES2560454T3/es active Active
- 2008-09-05 US US12/676,665 patent/US8632703B2/en not_active Expired - Fee Related
- 2008-09-05 AU AU2008296223A patent/AU2008296223B2/en not_active Ceased
- 2008-09-05 JP JP2010524167A patent/JP5530929B2/ja not_active Expired - Fee Related
- 2008-09-05 MX MX2010002471A patent/MX2010002471A/es active IP Right Grant
- 2008-09-05 CN CN200880105429.XA patent/CN101815773B/zh not_active Expired - Fee Related
- 2008-09-05 CA CA2921867A patent/CA2921867A1/en not_active Abandoned
- 2008-09-05 CA CA2695229A patent/CA2695229C/en not_active Expired - Fee Related
- 2008-09-05 EP EP08829661.1A patent/EP2188348B1/en not_active Not-in-force
- 2008-09-05 WO PCT/US2008/075345 patent/WO2009032983A1/en active Application Filing
- 2008-09-08 AR ARP080103895A patent/AR068235A1/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
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US20100243943A1 (en) | 2010-09-30 |
EP2188348B1 (en) | 2015-11-04 |
EP2188348A1 (en) | 2010-05-26 |
JP2010538151A (ja) | 2010-12-09 |
AU2008296223B2 (en) | 2013-07-04 |
US8632703B2 (en) | 2014-01-21 |
CA2695229C (en) | 2016-05-10 |
MX2010002471A (es) | 2010-03-26 |
BRPI0815462A2 (pt) | 2015-02-18 |
CN101815773A (zh) | 2010-08-25 |
CN101815773B (zh) | 2014-05-07 |
AR068235A1 (es) | 2009-11-11 |
CA2695229A1 (en) | 2009-03-12 |
KR20100065358A (ko) | 2010-06-16 |
WO2009032983A1 (en) | 2009-03-12 |
KR101527244B1 (ko) | 2015-06-08 |
CA2921867A1 (en) | 2009-03-12 |
ES2560454T3 (es) | 2016-02-19 |
AU2008296223A1 (en) | 2009-03-12 |
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