JP7383015B2 - HFO-1234yf及びプロピレンの共沸組成物 - Google Patents
HFO-1234yf及びプロピレンの共沸組成物 Download PDFInfo
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- JP7383015B2 JP7383015B2 JP2021518443A JP2021518443A JP7383015B2 JP 7383015 B2 JP7383015 B2 JP 7383015B2 JP 2021518443 A JP2021518443 A JP 2021518443A JP 2021518443 A JP2021518443 A JP 2021518443A JP 7383015 B2 JP7383015 B2 JP 7383015B2
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- hfo
- propylene
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- refrigerant
- acid
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- C09K5/00—Heat-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
- C09K5/02—Materials undergoing a change of physical state when used
- C09K5/04—Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
- C09K5/041—Materials 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
- C09K5/044—Materials 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
- C09K5/045—Materials 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 containing only fluorine as halogen
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25B—REFRIGERATION MACHINES, PLANTS OR SYSTEMS; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS
- F25B45/00—Arrangements for charging or discharging refrigerant
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- C09K2205/24—Only one single fluoro component present
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Description
本出願は、2018年10月4日に出願された米国特許仮出願第62/741261号の利益を主張するものであり、その全容が参照により本明細書に組み込まれる。
本発明は、HFO-1234yf及びプロピレン(R-290)の共沸及び近共沸組成物を対象とする。
本明細書で使用するとき、伝熱組成物という用語は、熱源からヒートシンクまで熱を運ぶために使用される組成物を意味する。
地球温暖化係数(GWP)は、1キログラムの二酸化炭素の排出と比較して、1キログラムの特定の温室効果ガスの大気排出に起因する相対的な地球温暖化への関与を推定するための指数である。GWPは、様々な対象期間について計算することができ、所与のガスの大気寿命の影響を示す。100年間の対象期間のGWPは、一般に、業界で参照される値であり、本明細書で使用されるものとする。流体混合物又は冷媒混合物については、各成分に関する個々のGWPに基づいて加重平均を計算することができる。国連気候変動政府間パネル(Intergovernmental Panel on Climate Control、IPCC)は、公式評価報告書(assessment report、AR)において、冷媒GWPのためのベッティング値を提供している。第4次評価報告書はAR4として表され、第5次評価報告書はA5として表される。規制主体(Regulating bodes)は、現在、正式な法制化の目的でAR4を使用している。
本発明の冷媒又は伝熱組成物は、潤滑剤と混合され、本発明の「完全な作動流体組成物」として使用することができる。本発明の伝熱流体又は作動流体、及び潤滑剤を含有する本発明の冷媒組成物は、安定剤、漏れ検出物質、他の有益な添加剤などの公知の添加剤を含有してもよい。得られる化合物の可燃性レベルに潤滑剤が影響を与えることも可能である。
HFC系冷媒は、二重結合の存在により、熱不安定性になりがちであり、極端な使用、取り扱い又は保管状況下で分解する場合がある。したがって、HFC系冷媒に安定剤を添加することが有利であり得る。安定剤としては、特に、ニトロメタン、アスコルビン酸、テレフタル酸、トルトリアゾール又はベンゾトリアゾールなどのアゾール、トコフェロール、ヒドロキノン、t-ブチルヒドロキノン、2,6-ジ-tert-ブチル-4-メチルフェノールなどのフェノール化合物、n-ブチルグリシジルエーテル、ヘキサンジオールジグリシジルエーテル、アリルグリシジルエーテル、ブチルフェニルグリシジルエーテルなどのエポキシド(場合により、フッ素化若しくはペルフッ素化アルキルエポキシド又はアルケニル若しくは芳香族エポキシド)、テルペン、例えばd-リモネン又はα及びβ-ピネンなど、ホスファイト、リン酸塩、ホスホン酸塩、チオール及びラクトンが挙げられる。
可燃性は、発火する及び/又は炎を伝播する、組成物の能力を意味するために使用される用語である。冷媒及び他の伝熱組成物又は作動流体について、燃焼下限濃度(lower flammability limit、「LFL」)とは、ASTM(American Society of Testing and Materials、米国材料検査協会)E681に定められている試験条件下で、組成物の均質混合物及び空気を通して炎を伝播することができる空気中における伝熱組成物の最低濃度である。燃焼上限濃度(upper flammability limit、「UFL」)とは、同じ試験条件下で、組成物の均質混合物及び空気を通して炎を伝播することができる、空気中における伝熱組成物の最高濃度である。
加熱モード:プロピレン
熱力学モデリングプログラム、熱サイクル3.0を使用して、HFO-1234yfと比較して、HFO-1234yf/プロピレンに対しブレンドの予想される性能をモデル化した。加熱モードで使用したモデル条件は以下のとおりであり、熱交換器#2は10℃刻みで変化させた。
冷却モード:プロピレン
熱力学モデリングプログラム、熱サイクル3.0を使用して、HFO-1234yf/プロピレンと比較して、HFO-1234yfに対してブレンドの予想される性能をモデル化した。冷却モードで使用したモデル条件は以下のとおりであり、熱交換器#2は10℃刻みで変化させた。
Claims (10)
- HEV、MHEV、PHEV、又はEVのヒートポンプシステムにおける冷媒組成物の使用であって、前記冷媒組成物は、
2,3,3,3-テトラフルオロプロペン(HFO-1234yf)及びプロピレン(R-1270)を含み、
前記組成物は、-30℃から40℃の温度範囲にわたって近共沸性であり、および、前記組成物は、-30℃から10℃までの温度で1.1ケルビン(K)未満の温度勾配を有する、使用。 - 前記組成物が-30℃~40℃の温度範囲にわたって共沸混合物様である、請求項1に記載の使用。
- 前記2,3,3,3-テトラフルオロプロペン(HFO-1234yf)濃度が、プロピレンNAL1の2,3,3,3-テトラフルオロプロペン(HFO-1234yf)濃度以上であり、
前記2,3,3,3-テトラフルオロプロペン(HFO-1234yf)濃度が、プロピレンNAH1の2,3,3,3-テトラフルオロプロペン(HFO-1234yf)濃度以下である、請求項1に記載の使用。 - 前記2,3,3,3-テトラフルオロプロペン(HFO-1234yf)濃度が、プロピレンALL1の2,3,3,3-テトラフルオロプロペン(HFO-1234yf)濃度以上であり、
前記2,3,3,3-テトラフルオロプロペン(HFO-1234yf)濃度が、プロピレンALH1の2,3,3,3-テトラフルオロプロペン(HFO-1234yf)濃度以下である、請求項1に記載の使用。 - 前記プロピレン(R-1270)が、前記全冷媒組成物に基づいて最大24重量%の量で存在する、請求項1に記載の使用。
- 前記プロピレン(R-1270)が、前記全冷媒組成物に基づいて1~10重量%の量で存在する、請求項5に記載の使用。
- 前記冷媒組成物の熱容量が、2,3,3,3-テトラフルオロプロペン(HFO-1234yf)単独の熱容量よりも2.9%~27.5%大きい、請求項1に記載の使用。
- 前記冷媒組成物の熱容量が、2,3,3,3-テトラフルオロプロペン(HFO-1234yf)単独の熱容量よりも2%~22%大きい、請求項1に記載の使用。
- 請求項1に記載の組成物の熱容量と、2,3,3,3-テトラフルオロプロペン(HFO-1234yf)の熱容量との比が、同じ温度及び圧力において1.05~1.50である、請求項1に記載の使用。
- 車両電気システムと組み合わせたHEV、MHEV、PHEV、EVのヒートポンプシステムにおける請求項1に記載の使用。
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Publication number | Priority date | Publication date | Assignee | Title |
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JP2012509392A (ja) | 2008-11-19 | 2012-04-19 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 2,3,3,3−テトラフルオロプロペンおよび炭化水素を含む組成物ならびにその使用 |
JP2012509380A (ja) | 2008-11-20 | 2012-04-19 | アルケマ フランス | 2,3,3,3−テトラフルオロプロペンを含む組成物、車両の加熱および/または空調方法 |
JP2015108504A (ja) | 2008-11-20 | 2015-06-11 | アルケマ フランス | 車両の暖房および/または空調方法 |
JP2016056374A (ja) | 2013-07-12 | 2016-04-21 | 旭硝子株式会社 | 熱サイクル用作動媒体、熱サイクルシステム用組成物および熱サイクルシステム |
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Publication number | Priority date | Publication date | Assignee | Title |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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JP2012509380A (ja) | 2008-11-20 | 2012-04-19 | アルケマ フランス | 2,3,3,3−テトラフルオロプロペンを含む組成物、車両の加熱および/または空調方法 |
JP2015108504A (ja) | 2008-11-20 | 2015-06-11 | アルケマ フランス | 車両の暖房および/または空調方法 |
JP2016056374A (ja) | 2013-07-12 | 2016-04-21 | 旭硝子株式会社 | 熱サイクル用作動媒体、熱サイクルシステム用組成物および熱サイクルシステム |
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