JP2011525209A - Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンの共沸および共沸混合物様組成物 - Google Patents
Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンの共沸および共沸混合物様組成物 Download PDFInfo
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Abstract
Description
本出願は、2008年6月20日出願の米国仮特許出願第61/074178号明細書、米国仮特許出願第61/074179号明細書および米国仮特許出願第61/074181号明細書の優先権を主張するものである。
Claims (13)
- (a)Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと、
(b)ジエチルエーテルと、から本質的になる組成物であって、前記ジエチルエーテルが前記Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブ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)Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと、及び
(b)ジエチルエーテルと、から本質的になる組成物であって、前記ジエチルエーテルが前記Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブ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)Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと、
(b)2−クロロプロパンと、から本質的になる組成物であって、前記2−クロロプロパンが前記Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブ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)Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと、
(b)2−クロロプロパンと、から本質的になる組成物であって、前記2−クロロプロパンが前記Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブ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)Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと、
(b)パーフルオロ(2−メチル−3−ペンタノン)と、から本質的になる組成物であって、前記パーフルオロ(2−メチル−3−ペンタノン)が前記Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブ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)Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと、
(b)パーフルオロ(2−メチル−3−ペンタノン)と、から本質的になる組成物であって、前記パーフルオロ(2−メチル−3−ペンタノン)が前記Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブ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、Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと、ジエチルエーテル、2−クロロプロパン、およびパーフルオロ(2−メチル−3−ペンタノン)からなる群から選択される成分とから本質的になる方法。
- 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、Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと、ジエチルエーテル、2−クロロプロパン、およびパーフルオロ(2−メチル−3−ペンタノン)からなる群から選択される成分とから本質的になる方法。
- 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、Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと、ジエチルエーテル、2−クロロプロパン、およびパーフルオロ(2−メチル−3−ペンタノン)からなる群から選択される成分とから本質的になる方法。
- 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、Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと、ジエチルエーテル、2−クロロプロパン、およびパーフルオロ(2−メチル−3−ペンタノン)からなる群から選択される成分とから本質的になる方法。
- 共沸もしくは共沸混合物様組成物を伝熱媒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、Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと、ジエチルエーテル、2−クロロプロパン、およびパーフルオロ(2−メチル−3−ペンタノン)からなる群から選択される成分とから本質的になる方法。
- 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、Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと、ジエチルエーテル、2−クロロプロパン、およびパーフルオロ(2−メチル−3−ペンタノン)からなる群から選択される成分とから本質的になる方法。
- 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、Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンと、ジエチルエーテル、2−クロロプロパン、およびパーフルオロ(2−メチル−3−ペンタノン)からなる群から選択される成分とから本質的になる方法。
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US7417908P | 2008-06-20 | 2008-06-20 | |
US7418108P | 2008-06-20 | 2008-06-20 | |
US7417808P | 2008-06-20 | 2008-06-20 | |
US61/074,179 | 2008-06-20 | ||
US61/074,178 | 2008-06-20 | ||
US61/074,181 | 2008-06-20 | ||
PCT/US2009/047912 WO2009155490A1 (en) | 2008-06-20 | 2009-06-19 | Azeotropic and azeotrope-like compositions of z-1,1,1,4,4,4-hexafluoro-2-butene |
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JP2014158872A Division JP5957493B2 (ja) | 2008-06-20 | 2014-08-04 | Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンの共沸および共沸混合物様組成物 |
JP2015174003A Division JP6051281B2 (ja) | 2008-06-20 | 2015-09-03 | Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンの共沸および共沸混合物様組成物 |
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JP2011525209A true JP2011525209A (ja) | 2011-09-15 |
JP5806111B2 JP5806111B2 (ja) | 2015-11-10 |
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JP2011514830A Expired - Fee Related JP5806111B2 (ja) | 2008-06-20 | 2009-06-19 | Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンの共沸および共沸混合物様組成物 |
JP2014158872A Expired - Fee Related JP5957493B2 (ja) | 2008-06-20 | 2014-08-04 | Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンの共沸および共沸混合物様組成物 |
JP2015174003A Active JP6051281B2 (ja) | 2008-06-20 | 2015-09-03 | Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンの共沸および共沸混合物様組成物 |
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JP2014158872A Expired - Fee Related JP5957493B2 (ja) | 2008-06-20 | 2014-08-04 | Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンの共沸および共沸混合物様組成物 |
JP2015174003A Active JP6051281B2 (ja) | 2008-06-20 | 2015-09-03 | Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンの共沸および共沸混合物様組成物 |
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EP (1) | EP2285930B1 (ja) |
JP (3) | JP5806111B2 (ja) |
KR (2) | KR101618900B1 (ja) |
CN (1) | CN102066521B (ja) |
AU (1) | AU2009259965B2 (ja) |
BR (1) | BRPI0909619A2 (ja) |
CA (2) | CA2725404A1 (ja) |
CO (1) | CO6280546A2 (ja) |
ES (1) | ES2568429T3 (ja) |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013514444A (ja) * | 2009-12-16 | 2013-04-25 | ハネウェル・インターナショナル・インコーポレーテッド | シス−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンの共沸混合物様の組成物 |
JP2015507039A (ja) * | 2011-12-22 | 2015-03-05 | ハネウェル・インターナショナル・インコーポレーテッド | cis−1−クロロ−3,3,3−トリフルオロプロペンを包含する共沸混合物様組成物 |
JP5805345B1 (ja) * | 2015-06-04 | 2015-11-04 | 積水化学工業株式会社 | フェノール樹脂発泡体 |
JP2017534704A (ja) * | 2014-09-16 | 2017-11-24 | ザ ケマーズ カンパニー エフシー リミテッド ライアビリティ カンパニー | Z−1,1,1,4,4,4−ヘキサフルオロ−2−ブテンとメチルパーフルオロプロピルエーテルとを含む共沸性又は共沸混合物様組成物 |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
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MX2011012954A (es) | 2009-06-02 | 2011-12-16 | Du Pont | Composiciones azeotropicas y similares a azeotropos de z-1,1,1,4,4,4-hexafluoro-2-buteno. |
US20110144216A1 (en) * | 2009-12-16 | 2011-06-16 | Honeywell International Inc. | Compositions and uses of cis-1,1,1,4,4,4-hexafluoro-2-butene |
AU2013204160B2 (en) * | 2009-12-16 | 2015-07-02 | Honeywell International Inc. | Azeotrope-like compositions of cis-1,1,1,4,4,4-hexafluoro-2-butene |
AU2015234339B2 (en) * | 2009-12-16 | 2017-03-16 | Honeywell International Inc. | Azeotrope-like compositions of cis-1,1,1,4,4,4-hexafluoro-2-butene |
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Also Published As
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JP2014224267A (ja) | 2014-12-04 |
EP2285930A1 (en) | 2011-02-23 |
ES2568429T3 (es) | 2016-04-29 |
CA2944302C (en) | 2017-11-21 |
JP6051281B2 (ja) | 2016-12-27 |
JP2015227467A (ja) | 2015-12-17 |
MX2010014094A (es) | 2011-01-21 |
AU2009259965A1 (en) | 2009-12-23 |
CN102066521B (zh) | 2013-11-13 |
PL2285930T3 (pl) | 2016-07-29 |
KR20110038044A (ko) | 2011-04-13 |
JP5957493B2 (ja) | 2016-07-27 |
WO2009155490A1 (en) | 2009-12-23 |
EP2285930B1 (en) | 2016-01-27 |
CN102066521A (zh) | 2011-05-18 |
KR101618900B1 (ko) | 2016-05-09 |
KR20160040314A (ko) | 2016-04-12 |
CO6280546A2 (es) | 2011-05-20 |
BRPI0909619A2 (pt) | 2015-09-22 |
CA2944302A1 (en) | 2009-12-23 |
AU2009259965B2 (en) | 2015-08-27 |
CA2725404A1 (en) | 2009-12-23 |
JP5806111B2 (ja) | 2015-11-10 |
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