JPWO2016171264A1 - 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 - Google Patents
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 Download PDFInfo
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- JPWO2016171264A1 JPWO2016171264A1 JP2017514218A JP2017514218A JPWO2016171264A1 JP WO2016171264 A1 JPWO2016171264 A1 JP WO2016171264A1 JP 2017514218 A JP2017514218 A JP 2017514218A JP 2017514218 A JP2017514218 A JP 2017514218A JP WO2016171264 A1 JPWO2016171264 A1 JP WO2016171264A1
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- Prior art keywords
- heat cycle
- cycle system
- working medium
- refrigerating machine
- composition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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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
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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
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Abstract
Description
[2]前記1−クロロ−2,3,3,3−テトラフルオロプロペンは、(Z)−1−クロロ−2,3,3,3−テトラフルオロプロペンおよび(E)−1−クロロ−2,3,3,3−テトラフルオロプロペンを、(Z)−1−クロロ−2,3,3,3−テトラフルオロプロペン:(E)−1−クロロ−2,3,3,3−テトラフルオロプロペンで示される質量比で、51:49〜100:0の割合で含む[1]に記載の熱サイクルシステム用組成物。
[3]前記冷凍機油が、エステル系冷凍機油、エーテル系冷凍機油、炭化水素系冷凍機油、ナフテン系冷凍機油からなる群より選ばれる少なくとも1種の油を含む[1]または[2]に記載の熱サイクルシステム用組成物。
[4]前記冷凍機油が、二塩基酸エステル、ポリオールエステル、コンプレックスエステル、ポリオール炭酸エステル、ポリビニルエーテル、ポリアルキレングリコール、アルキルベンゼンおよびナフテン基油からなる群より選ばれる少なくとも1種の化合物を含む[3]に記載の熱サイクルシステム用組成物。
[5]前記冷凍機油の40℃における動粘度が1mm2/s以上750mm2/s以下である[1]〜[4]のいずれかに記載の熱サイクルシステム用組成物。
[6]前記冷凍機油は、炭素原子と酸素原子とを、炭素原子/酸素原子で示されるモル比で、2.0以上7.5以下の割合で含む[1]〜[5]のいずれかに記載の熱サイクルシステム用組成物。
[7]前記熱サイクル用作動媒体がさらに飽和のヒドロフルオロカーボンを含む[1]〜[6]のいずれかに記載の熱サイクルシステム用組成物。
[8]前記熱サイクル用作動媒体がさらにヒドロフルオロオレフィンを含む[1]〜[7]のいずれかに記載の熱サイクルシステム用組成物。
[9]前記熱サイクル用作動媒体がさらに前記1−クロロ−2,3,3,3−テトラフルオロプロペン以外のヒドロクロロフルオロオレフィンを含む[1]〜[8]のいずれかに記載の熱サイクルシステム用組成物。
[10]前記熱サイクル用作動媒体は、前記1−クロロ−2,3,3,3−テトラフルオロプロペンを10質量%以上100質量%以下含む[1]〜[9]のいずれかに記載の熱サイクルシステム用組成物。
[11]前記熱サイクル用作動媒体は、前記1−クロロ−2,3,3,3−テトラフルオロプロペンを20質量%以上95質量%以下含む[10]に記載の熱サイクルシステム用組成物。
[12][1]〜[11]のいずれかに記載の熱サイクルシステム用組成物を用いた、熱サイクルシステム。
[13]前記熱サイクルシステムが、冷凍・冷蔵機器、空調機器、発電システム、熱輸送装置または二次冷却機である[12]に記載の熱サイクルシステム。
[14]前記熱サイクルシステムが、遠心式冷凍機である[12]に記載の熱サイクルシステム。
[15]前記熱サイクルシステムが、低圧型遠心式冷凍機である[12]に記載の熱サイクルシステム。
熱サイクルシステム用組成物は、HCFO−1224ydを含む熱サイクル用作動媒体と、冷凍機油とを含む。
本発明の熱サイクルシステム用組成物は熱サイクル用作動媒体として、HCFO−1224ydを含有する。熱サイクル用作動媒体は、HCFO−1224ydに加えて、必要に応じて、後述する任意成分を含んでいてもよい。熱サイクル用作動媒体は、HCFO−1224ydを、好ましくは10質量%以上、より好ましくは10質量%以上100質量%以下、一層好ましくは20質量%以上100質量%以下、さらに好ましくは40質量%以上100質量%以下、最も好ましくは60質量%以上100質量%以下含む。熱サイクル用作動媒体は、混合物にする場合は、HCFO−1224ydを20質量%以上95質量%以下含むことが好ましい。
HCFO−1224ydは、上記したように、燃焼性を抑えるハロゲンと、大気中のOHラジカルによって分解されやすい炭素−炭素二重結合とをその分子中に有している。そのため、HCFO−1224ydは、燃焼性が抑えられ、オゾン層への影響が少なく、かつ地球温暖化への影響が少ない熱サイクル用作動媒体である。
熱サイクル用作動媒体は、本発明の効果を損なわない範囲で、HCFO−1224yd以外に、通常作動媒体として用いられる化合物を任意に含有してもよい。このような任意の化合物(任意成分)としては、例えば、HFC、HFO、HCFO−1224yd以外のHCFO、HCFO−1224ydとともに気化、液化するHFCとHFOとHCFO以外の他の成分等が挙げられる。任意成分としては、HFC、HFO、HCFO−1224yd以外のHCFOが好ましい。
熱サイクル用作動媒体が任意成分を含有する場合、HCFO−1224ydと任意成分が共沸組成である場合を除いて、熱サイクル用作動媒体は相当の温度勾配を有する。熱サイクル用作動媒体の温度勾配は、任意成分の種類およびHCFO−1224ydと任意成分との混合割合により異なる。
HFCは、熱サイクルシステムのサイクル性能(能力)を向上させる成分である。
HFOは、熱サイクルシステムのサイクル性能(能力)を向上させる成分である。
HCFO−1224yd以外の任意成分としてのHCFOについても、上記HFOと同様の観点から選択されることが好ましい。なお、HCFO−1224yd以外のHCFOのGWPは、HFCに比べて桁違いに低い。したがって、HCFO−1224ydと組み合わせるHCFO−1224yd以外のHCFOとしては、GWPを考慮するよりも、上記熱サイクル用作動媒体として、サイクル性能を向上させ、かつ温度勾配を適切な範囲にとどめることに特に留意して、適宜選択されることが好ましい。
熱サイクルシステム用組成物に用いる熱サイクル用作動媒体は、上記任意成分以外に、二酸化炭素、炭化水素、クロロフルオロオレフィン(CFO)等のその他の任意成分を含有してもよい。その他の任意成分としては、オゾン層への影響が少なく、かつ地球温暖化への影響が小さい成分が好ましい。
熱サイクルシステム用組成物には、上記熱サイクル用作動媒体に加え、HCFO−1224ydを含む熱サイクル用作動媒体の潤滑特性を改善可能な冷凍機油が含まれる。
エステル系冷凍機油の基油成分としては、化学的な安定性の面で、二塩基酸と一価アルコールとの二塩基酸エステル、ポリオールと脂肪酸とのポリオールエステル、ポリオールと多価塩基酸と一価アルコール(又は脂肪酸)とのコンプレックスエステル、ポリオール炭酸エステル等が挙げられる。
二塩基酸エステルとしては、シュウ酸、マロン酸、コハク酸、グルタル酸、アジピン酸、ピメリン酸、スベリン酸、アゼライン酸、セバシン酸、フタル酸、イソフタル酸、テレフタル酸等の二塩基酸、特に、炭素数5以上10以下の二塩基酸(グルタル酸、アジピン酸、ピメリン酸、スベリン酸、アゼライン酸、セバシン酸等)と、直鎖または分岐アルキル基を有する炭素数1以上15以下の一価アルコール(メタノール、エタノール、プロパノール、ブタノール、ペンタノール、ヘキサノール、ヘプタノール、オクタノール、ノナノール、デカノール、ウンデカノール、ドデカノール、トリデカノール、テトラデカノール、ペンタデカノール等)とのエステルが好ましい。この二塩基酸エステル系冷凍機油としては、具体的には、グルタル酸ジトリデシル、アジピン酸ジ(2−エチルヘキシル)、アジピン酸ジイソデシル、アジピン酸ジトリデシル、セバシン酸ジ(3−エチルヘキシル)等が挙げられる。
ポリオールエステルとは、多価アルコール(ポリオールともいう。)と脂肪酸(カルボン酸)とから合成されるエステルであり、ポリオールエステルを構成する炭素原子と酸素原子との比率(炭素原子/酸素原子)は、モル比で、2.0以上7.5以下、好ましくは3.2以上5.8以下である。
コンプレックスエステルとは、脂肪酸および二塩基酸と、一価アルコールおよびポリオールとのエステルである。脂肪酸、二塩基酸、一価アルコール、ポリオールとしては、上述と同様のものを用いることができる。
ポリオール炭酸エステルとは、炭酸とポリオールとのエステルである。ポリオールとしては、ジオール(上述と同様のもの)を単独重合または共重合したポリグリコール(ポリアルキレングリコール、そのエーテル化合物、それらの変性化合物等)、ポリオール(上述と同様のもの)、ポリオールにポリグリコールを付加したもの等が挙げられる。
エーテル系冷凍機油の基油成分としては、ポリビニルエーテル、ポリアルキレングリコール等が挙げられる。
ポリビニルエーテルとしては、ビニルエーテルモノマーを重合して得られたもの、ビニルエーテルモノマーとオレフィン性二重結合を有する炭化水素モノマーとを共重合して得られたもの、およびポリビニルエーテルと、アルキレングリコールもしくはポリアルキレングリコール、またはそれらのモノエーテルとの共重合体がある。
ビニルエーテルモノマーは、1種を単独で用いてもよく、2種以上を組み合わせて用いてもよい。オレフィン性二重結合を有する炭化水素モノマーとしては、エチレン、プロピレン、各種ブテン、各種ペンテン、各種ヘキセン、各種ヘプテン、各種オクテン、ジイソブチレン、トリイソブチレン、スチレン、α−メチルスチレン、各種アルキル置換スチレン等が挙げられる。オレフィン性二重結合を有する炭化水素モノマーは、1種を単独で用いてもよく、2種以上を組み合わせて用いてもよい。
本発明の熱サイクルシステム用組成物に冷凍機油の基油成分として用いられる上記一般式(1)で表される構成単位を有するポリビニルエーテルは、その末端を本開示例に示す方法及び公知の方法により、所望の構造に変換することができる。変換する基としては、飽和の炭化水素基、エーテル基、ヒドロキシ基、ケトン基、アミド基、ニトリル基などを挙げることができる。
本実施形態におけるポリビニルエーテルは、上記したモノマーをラジカル重合、カチオン重合、放射線重合などによって製造することができる。重合反応終了後、必要に応じて通常の分離・精製方法を施すことにより、目的とする一般式(1)で表される構造単位を有するポリビニルエーテルが得られる。
ポリアルキレングリコールとしては、炭素数2以上4以下のアルキレンオキシド(エチレンオキシド、プロピレンオキシド等)を、水や水酸化アルカリを開始剤として重合させる方法等により得られたものが挙げられる。また、ポリアルキレングリコールの水酸基をエーテル化したものであってもよい。ポリアルキレングリコール中のオキシアルキレン単位は、1分子中において同一であってもよく、2種以上のオキシアルキレン単位が含まれていてもよい。1分子中に少なくともオキシプロピレン単位が含まれることが好ましい。
炭化水素系冷凍機油の基油成分としては、アルキルベンゼンを用いることができる。
鉱油系冷凍機油としては、パラフィン系冷凍機油、ナフテン系冷凍機油のうち、熱サイクル用作動媒体と相溶性の高いナフテン系冷凍機油を用いることができる。
熱サイクルシステム用組成物は、その他、本発明の効果を阻害しない範囲で公知の任意成分を含有できる。このような任意成分としては、例えば、漏れ検出物質が挙げられ、この任意に含有する漏れ検出物質としては、紫外線蛍光染料、臭気ガスや臭いマスキング剤等が挙げられる。
本発明の熱サイクルシステムは、本発明の熱サイクルシステム用組成物を用いたシステムである。本発明の熱サイクルシステムは、凝縮器で得られる温熱を利用するヒートポンプシステムであってもよく、蒸発器で得られる冷熱を利用する冷凍サイクルシステムであってもよい。
(ii)圧縮機11から排出された熱サイクル用作動媒体の蒸気Bを凝縮器12にて流体Fによって冷却し、液化して低温高圧の熱サイクル用作動媒体Cとする。この際、流体Fは加熱されて流体F’となり、凝縮器12から排出される。以下、「BC過程」という。
(iii)凝縮器12から排出された熱サイクル用作動媒体Cを膨張弁13にて膨張させて低温低圧の熱サイクル用作動媒体Dとする。以下、「CD過程」という。
(iv)膨張弁13から排出された熱サイクル用作動媒体Dを蒸発器14にて負荷流体Eによって加熱して高温低圧の熱サイクル用作動媒体の蒸気Aとする。この際、負荷流体Eは冷却されて負荷流体E’となり、蒸発器14から排出される。以下、「DA過程」という。
COP=Q/圧縮仕事=(hA−hD)/(hB−hA) …(B)
冷凍機油2:ポリビニルエーテルを主成分とする冷凍機油(商品名:ダフニーハーメチックオイルFVC68D、出光興産株式会社製品;40℃における動粘度が68mm2/s)
冷凍機油3:ポリアルキレングリコールを主成分とする冷凍機油(商品名:ND−8、株式会社デンソー社製品;40℃における動粘度が41mm2/s)
冷凍機油4:アルキルベンゼンを主成分とする冷凍機油(商品名:アトモスN22、JX日鉱日石エネルギー株式会社製品;40℃における動粘度が21.5mm2/s)
冷凍機油5:ナフテン系高級冷凍機油(商品名:スニソ4GS、出光興産株式会社製品;40℃における動粘度が68mm2/s)
図1のような熱サイクルシステムに、各例で得られた熱サイクルシステム用組成物を入れ、熱サイクルシステムの連続運転を行った。熱サイクルシステム用組成物の循環状態を評価するために、熱サイクルシステムにおける蒸発器から圧縮機への流路の一部をガラス配管とした。このガラス配管から内部を観察して、熱サイクルシステム内の熱サイクルシステム用組成物の循環状態を評価した。熱サイクルシステム用組成物の循環状態は、目視にて以下の基準により評価した。
A:冷凍機油の循環が確認できた。
B:冷凍機油の循環は見られるが循環量が不十分。
C:冷凍機油の循環が確認できない。
安定性試験は、循環状態が良好な例1〜265の熱サイクルシステム用組成物に対して、JIS K 2211に記された「冷媒と冷凍機油の化学的安定性試験方法(オートクレーブ)」に準拠して実施した。
b)銅:タフピッチ銅(JIS H3100に定められたもの、合金番号C1100、記号C1100P)の試験片、30mm×25mm×厚さ2mm
c)アルミニウム:純アルミニウム(JIS H4000に定められたもの、合金番号1050、記号A1050P)の試験片、30mm×25mm×厚さ2mm
安定性試験後の熱サイクル用作動媒体の酸分量測定は、JIS K1560(1,1,1,2−テトラフルオロエタン(HFC−134a))に準拠して実施した。
酸分量測定後、熱サイクル用作動媒体を抜き出した耐圧容器に残った冷凍機油を取り出し、ASTM−D156に準拠して冷凍機油の色相を評価した。ここで、L値は数値が大きいほど着色度合いが大きいため、数値が低いほど好ましい。ここではL3.5以下が好ましく、L3.0以下がより好ましく、L2.5以下がさらに好ましい。
触媒の外観変化は、上記安定性試験後の触媒の金属片の外観を目視で確認し、以下の基準により評価した。
B:光沢なしまたは黒く変色
Claims (15)
- 1−クロロ−2,3,3,3−テトラフルオロプロペンを含む熱サイクル用作動媒体と冷凍機油とを含む熱サイクルシステム用組成物。
- 前記1−クロロ−2,3,3,3−テトラフルオロプロペンが、(Z)−1−クロロ−2,3,3,3−テトラフルオロプロペンおよび(E)−1−クロロ−2,3,3,3−テトラフルオロプロペンを、(Z)−1−クロロ−2,3,3,3−テトラフルオロプロペン:(E)−1−クロロ−2,3,3,3−テトラフルオロプロペンで示される質量比で、51:49〜100:0の割合で含む請求項1に記載の熱サイクルシステム用組成物。
- 前記冷凍機油が、エステル系冷凍機油、エーテル系冷凍機油、炭化水素系冷凍機油、ナフテン系冷凍機油からなる群より選ばれる少なくとも1種の油を含む請求項1または2に記載の熱サイクルシステム用組成物。
- 前記冷凍機油が、二塩基酸エステル、ポリオールエステル、コンプレックスエステル、ポリオール炭酸エステル、ポリビニルエーテル、ポリアルキレングリコール、アルキルベンゼンおよびナフテン基油からなる群より選ばれる少なくとも1種の化合物を含む請求項3に記載の熱サイクルシステム用組成物。
- 前記冷凍機油の40℃における動粘度が1mm2/s以上750mm2/s以下である請求項1〜4のいずれか1項に記載の熱サイクルシステム用組成物。
- 前記冷凍機油は、炭素原子と酸素原子とを、炭素原子/酸素原子で示されるモル比で、2.0以上7.5以下の割合で含む請求項1〜5のいずれか1項に記載の熱サイクルシステム用組成物。
- 前記熱サイクル用作動媒体がさらに飽和のヒドロフルオロカーボンを含む請求項1〜6のいずれか1項に記載の熱サイクルシステム用組成物。
- 前記熱サイクル用作動媒体がさらにヒドロフルオロオレフィンを含む請求項1〜7のいずれか1項に記載の熱サイクルシステム用組成物。
- 前記熱サイクル用作動媒体がさらに前記1−クロロ−2,3,3,3−テトラフルオロプロペン以外のヒドロクロロフルオロオレフィンを含む請求項1〜8のいずれか1項に記載の熱サイクルシステム用組成物。
- 前記熱サイクル用作動媒体は、前記1−クロロ−2,3,3,3−テトラフルオロプロペンを10質量%以上100質量%以下含む請求項1〜9のいずれか1項に記載の熱サイクルシステム用組成物。
- 前記熱サイクル用作動媒体は、前記1−クロロ−2,3,3,3−テトラフルオロプロペンを20質量%以上95質量%以下含む請求項10に記載の熱サイクルシステム用組成物。
- 請求項1〜11のいずれか1項に記載の熱サイクルシステム用組成物を用いた、熱サイクルシステム。
- 前記熱サイクルシステムが、冷凍・冷蔵機器、空調機器、発電システム、熱輸送装置または二次冷却機である請求項12に記載の熱サイクルシステム。
- 前記熱サイクルシステムが、遠心式冷凍機である請求項12に記載の熱サイクルシステム。
- 前記熱サイクルシステムが、低圧型遠心式冷凍機である請求項12に記載の熱サイクルシステム。
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WO2017145895A1 (ja) * | 2016-02-24 | 2017-08-31 | Jxエネルギー株式会社 | 冷凍機油 |
US11505760B2 (en) | 2016-02-24 | 2022-11-22 | Eneos Corporation | Refrigerator oil |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012157763A1 (ja) * | 2011-05-19 | 2012-11-22 | 旭硝子株式会社 | 作動媒体および熱サイクルシステム |
WO2012157765A1 (ja) * | 2011-05-19 | 2012-11-22 | 旭硝子株式会社 | 作動媒体および熱サイクルシステム |
WO2012157764A1 (ja) * | 2011-05-19 | 2012-11-22 | 旭硝子株式会社 | 作動媒体および熱サイクルシステム |
WO2014080868A1 (ja) * | 2012-11-20 | 2014-05-30 | 旭硝子株式会社 | ランキンサイクル用作動媒体およびランキンサイクルシステム |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009151669A1 (en) * | 2008-03-07 | 2009-12-17 | Arkema Inc. | Halogenated alkene heat transfer compositions with improved oil return |
WO2010085545A1 (en) * | 2009-01-26 | 2010-07-29 | Chemtura Corporation | Production of polyol ester lubricants for refrigeration systems |
CA2788053A1 (en) * | 2010-01-25 | 2011-07-28 | Arkema Inc. | Heat transfer composition of oxygenated lubricant with hydrofluoroolefin and hydrochlorofluoroolefin refrigerants |
WO2013059550A2 (en) * | 2011-10-20 | 2013-04-25 | E. I. Du Pont De Nemours And Company | Azeotrope-like compositions of e-1-chloro-2,3,3,3-tetrafluoropropene and uses thereof |
JP6019759B2 (ja) * | 2012-05-30 | 2016-11-02 | セントラル硝子株式会社 | フルオロアルケンを含有する熱伝達媒体 |
US9766919B2 (en) * | 2015-03-05 | 2017-09-19 | Vmware, Inc. | Methods and apparatus to select virtualization environments during deployment |
-
2016
- 2016-04-22 EP EP16783285.6A patent/EP3287503A4/en not_active Withdrawn
- 2016-04-22 CN CN201680023584.1A patent/CN107532071A/zh active Pending
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-
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- 2017-10-24 US US15/791,649 patent/US20180066170A1/en not_active Abandoned
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012157763A1 (ja) * | 2011-05-19 | 2012-11-22 | 旭硝子株式会社 | 作動媒体および熱サイクルシステム |
WO2012157765A1 (ja) * | 2011-05-19 | 2012-11-22 | 旭硝子株式会社 | 作動媒体および熱サイクルシステム |
WO2012157764A1 (ja) * | 2011-05-19 | 2012-11-22 | 旭硝子株式会社 | 作動媒体および熱サイクルシステム |
WO2014080868A1 (ja) * | 2012-11-20 | 2014-05-30 | 旭硝子株式会社 | ランキンサイクル用作動媒体およびランキンサイクルシステム |
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EP3287503A1 (en) | 2018-02-28 |
US20180066170A1 (en) | 2018-03-08 |
WO2016171264A1 (ja) | 2016-10-27 |
JP6693513B2 (ja) | 2020-05-13 |
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