JP2955598B1 - Azeotropic composition and azeotrope-like composition containing 2,2,1,1-tetrafluoroethyl 2 ', 2', 2'-trifluoroethyl ether - Google Patents

Azeotropic composition and azeotrope-like composition containing 2,2,1,1-tetrafluoroethyl 2 ', 2', 2'-trifluoroethyl ether

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Publication number
JP2955598B1
JP2955598B1 JP10188302A JP18830298A JP2955598B1 JP 2955598 B1 JP2955598 B1 JP 2955598B1 JP 10188302 A JP10188302 A JP 10188302A JP 18830298 A JP18830298 A JP 18830298A JP 2955598 B1 JP2955598 B1 JP 2955598B1
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Prior art keywords
composition
weight
azeotropic
hfe
polyol
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JP10188302A
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JP2000007603A (en
Inventor
良一 玉井
直門 高田
博志 山本
章 関屋
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National Institute of Advanced Industrial Science and Technology AIST
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Agency of Industrial Science and Technology
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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

【要約】 【課題】 地球環境への影響が最小限であり、かつ性能
の高いCFC、HCFCの代替物を提供する。 【解決手段】 CHF2CF2OCH2CF3(49から7
3重量%)とシクロペンタン(51から27重量%)か
らなる共沸組成物または共沸様組成物。
An object of the present invention is to provide a high performance alternative to CFC and HCFC that has minimal impact on the global environment. SOLUTION: CHF 2 CF 2 OCH 2 CF 3 (49 to 7)
Azeotropic or azeotrope-like composition consisting of 3% by weight) and cyclopentane (51 to 27% by weight).

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、共沸組成物及び共
沸様組成物に関するものである。
[0001] The present invention relates to an azeotropic composition and an azeotropic composition.

【0002】[0002]

【従来の技術】従来、冷媒、発泡剤、溶剤、洗浄剤、伝
熱媒体、作動流体、反応溶媒、塗料用溶剤,抽出剤、水
切り剤、乾燥剤等として、クロロフルオロカーボン類
(CFC)、ヒドロフルオロカーボン類(HCFC)が
広く用いられていた。しかしこのCFC類、HCFC類
は、成層圏のオゾン層を破壊し、人類を含む地球上の生
態系に重大な悪影響を及ぼすことが指摘され、現在、そ
の製造が禁止もしくは制限されている。このような問題
に対応するために、大気中に放出された場合にもオゾン
層を破壊しないCFC類、HCFC類の代替化合物が求
められている。冷媒、発泡剤、溶剤、洗浄剤、伝熱媒
体、作動流体、反応溶媒、塗料用溶剤,抽出剤、水切り
剤、乾燥剤等の用途の代替化合物として、水系、ハイド
ロカーボン系(HC系)、ハイドロフルオロカーボン系
(HFC系)、ハイドロフルオロエーテル系(HFE
系)等が数多く提案されている。水系の場合、主に溶
剤、洗浄剤等の用途において多く提案されている。水系
はその多くが不燃性であり、地球温暖化、成層圏のオゾ
ン層破壊等の環境への影響が少ないが、その性能が十分
でない場合があり、また排水処理等の設備が必要になる
問題点が残されている。HC系の場合、主に冷媒、発泡
剤、溶剤、洗浄剤、伝熱媒体、作動流体、反応溶媒、塗
料用溶剤,抽出剤、水切り剤、乾燥剤等の広い分野の用
途で提案されている。HC系の利点として、地球温暖
化、成層圏のオゾン層破壊等の影響は少ないが、これら
の多くは可燃性であり、安全性が懸念されている。ま
た、発泡剤の分野ではシクロペンタン等が提案されてい
るが、その気体の熱伝導率が高いので、冷蔵庫等の断熱
用ポリウレタンフォームの発泡剤として使用した場合、
断熱性能が低くなる。このことは、消費電力の増加を導
き、間接的に地球温暖化に影響することになる。HFC
系の場合も冷媒、発泡剤、溶剤、洗浄剤、伝熱媒体、作
動流体、反応溶媒、塗料用溶剤,抽出剤、水切り剤、乾
燥剤等の広い分野の用途で提案されている。HFC系は
塩素原子、沃素原子、臭素原子等のオゾンを破壊する原
子を含まないので、オゾン層への影響はゼロに近い。し
かし、不燃性のHFCの多くは大気寿命が長く、地球温
暖化への影響が懸念されている。HFE系の場合も冷
媒、発泡剤、溶剤、洗浄剤、伝熱媒体、作動流体、反応
溶媒、塗料用溶剤,抽出剤、水切り剤、乾燥剤等の広い
分野の用途で提案されている。HFE系も塩素原子、沃
素原子、臭素原子等のオゾンを破壊する原子を含まない
ので、オゾン層への影響はゼロに近い。また、推算によ
ると水素を複数持つHFEは大気中のOHラジカルとの
反応性が比較的早く大気寿命が短いので、地球温暖化へ
の影響も少ない。しかし、HFEを単独で使用した場
合、必要とする性能が十分に発揮されない場合がある。
複数のHFEを混合した場合、ポリオールとの相溶性、
冷媒特性、洗浄性、表面張力、気体の熱伝導率等のCF
C、HCFC等代替物として要求される物性が改善され
るケースが多い。しかし、非共沸で混合した場合、以下
のような問題がある。例えば、洗浄用途の場合、洗浄中
に洗浄剤の蒸発が起こった時、洗浄液の組成が変化し、
安定した操業が困難になる。冷媒の場合も同様に冷媒の
リークによって組成が変化し、ヒートポンプ性能が低下
する。また、発泡用途の場合、その沸点差により、均一
な発泡が困難となる。特に、電気冷蔵庫等の断熱を目的
とした硬質ポリウレタンフォームの製造において、発泡
の均一性はその断熱性能に大きく影響を及ぼす。また、
シクロペンタンは沸点が高くより室温に近い沸点を持つ
発泡剤が望まれている。
2. Description of the Related Art Conventionally, chlorofluorocarbons (CFCs), hydrofluorocarbons (CFCs), hydrophobes, solvents, detergents, heat transfer media, working fluids, reaction solvents, paint solvents, extractants, drainers, and desiccants have been used. Fluorocarbons (HCFCs) have been widely used. However, it has been pointed out that these CFCs and HCFCs destroy the stratospheric ozone layer and have serious adverse effects on ecosystems on the earth, including humans, and their production is currently banned or restricted. In order to cope with such a problem, there is a demand for alternative compounds to CFCs and HCFCs that do not destroy the ozone layer even when released into the atmosphere. Water-based, hydrocarbon-based (HC), and alternative compounds for applications such as refrigerants, foaming agents, solvents, cleaning agents, heat transfer media, working fluids, reaction solvents, paint solvents, extractants, drainers, and desiccants Hydrofluorocarbon (HFC), Hydrofluoroether (HFE)
And many others have been proposed. In the case of aqueous systems, many proposals have been made mainly for uses such as solvents and cleaning agents. Many of the water systems are nonflammable and have little effect on the environment, such as global warming and stratospheric ozone depletion, but their performance may not be sufficient, and equipment such as wastewater treatment is required. Is left. In the case of the HC system, it has been proposed for use in a wide range of fields such as refrigerants, foaming agents, solvents, cleaning agents, heat transfer media, working fluids, reaction solvents, paint solvents, extractants, drainers, and desiccants. . As an advantage of the HC system, there are few effects such as global warming and destruction of the ozone layer in the stratosphere. In the field of foaming agents, cyclopentane and the like have been proposed, but since the gas has a high thermal conductivity, when used as a foaming agent for insulating polyurethane foam such as refrigerators,
Insulation performance decreases. This leads to increased power consumption and indirectly affects global warming. HFC
In the case of a system, it is proposed for use in a wide range of fields such as a refrigerant, a foaming agent, a solvent, a cleaning agent, a heat transfer medium, a working fluid, a reaction solvent, a coating solvent, an extractant, a drainer, and a desiccant. Since the HFC system does not contain chlorine, iodine, bromine and other atoms that destroy ozone, the effect on the ozone layer is almost zero. However, many nonflammable HFCs have a long atmospheric life, and there is a concern that they will affect global warming. Also in the case of the HFE system, it has been proposed for use in a wide range of fields such as a refrigerant, a foaming agent, a solvent, a cleaning agent, a heat transfer medium, a working fluid, a reaction solvent, a coating solvent, an extractant, a drainer, and a drying agent. Since the HFE system does not include atoms that destroy ozone, such as chlorine, iodine, and bromine, the effect on the ozone layer is almost zero. According to the estimation, HFE having a plurality of hydrogens has relatively little reactivity with OH radicals in the atmosphere and a short life span in the atmosphere, and thus has little effect on global warming. However, when HFE is used alone, the required performance may not be sufficiently exhibited.
When a plurality of HFEs are mixed, compatibility with the polyol,
CF such as refrigerant characteristics, detergency, surface tension, and thermal conductivity of gas
In many cases, physical properties required as substitutes such as C and HCFC are improved. However, when mixed non-azeotropically, there are the following problems. For example, in the case of cleaning applications, when evaporation of the cleaning agent occurs during cleaning, the composition of the cleaning liquid changes,
Stable operation becomes difficult. Similarly, in the case of the refrigerant, the composition changes due to the leakage of the refrigerant, and the heat pump performance decreases. Further, in the case of foaming applications, uniform foaming becomes difficult due to the difference in boiling points. Particularly, in the production of a rigid polyurethane foam for heat insulation of an electric refrigerator or the like, the uniformity of foaming has a great influence on the heat insulation performance. Also,
Cyclopentane is desired to have a blowing agent having a high boiling point and a boiling point closer to room temperature.

【0003】[0003]

【発明が解決しようとする課題】本発明は、地球環境へ
の影響が最小限であり、かつ性能の高いCFC、HCF
Cの代替物を提供することをその課題とする。
SUMMARY OF THE INVENTION The present invention provides a high performance CFC or HCF with minimal impact on the global environment.
The task is to provide an alternative to C.

【0004】[0004]

【課題を解決するための手段】本発明者らは、前記の課
題を解決すべく鋭意研究を重ねた結果、本発明を完成す
るに至った。本発明によれば、すなわち、HFE類のコ
ードを、 HFE−347pc−f:CHF2CF2OCH2CF3 と定義したとき、HFE−347pc−f(49から7
3重量%)とシクロペンタン(51から27重量%)か
らなる共沸組成物または共沸様組成物、好ましくはHF
E−347pc−f(55から68重量%)とシクロペ
ンタン(45から32重量%)からなる共沸組成物また
は共沸様組成物、およびHFE−347pc−f(38
から64重量%)とn−ペンタン(62から36重量
%)からなる共沸組成物または共沸様組成物、好ましく
はHFE−347pc−f(45から58重量%)とn
−ペンタン(55から42重量%)からなる共沸組成物
または共沸様組成物が提供される。
Means for Solving the Problems The present inventors have made intensive studies to solve the above-mentioned problems, and as a result, have completed the present invention. According to the present invention, that is, when the code of the HFEs is defined as HFE-347pc-f: CHF 2 CF 2 OCH 2 CF 3 , HFE-347pc-f (49 to 7)
Azeotropic or azeotrope-like composition consisting of cyclopentane (51 to 27% by weight), preferably HF
An azeotropic or azeotrope-like composition consisting of E-347pc-f (55 to 68% by weight) and cyclopentane (45 to 32% by weight), and HFE-347pc-f (38
Azeotropic or azeotrope-like composition consisting of n-pentane (62 to 36% by weight) and n-pentane (62 to 36% by weight), preferably HFE-347pc-f (45 to 58% by weight) and n
An azeotropic or azeotrope-like composition comprising pentane (55 to 42% by weight) is provided.

【0005】[0005]

【発明の実施の形態】以下、本発明による共沸及び共沸
組成物様組成物を詳細に説明する。なお、共沸組成物と
は、一定圧力下で液相と気相の組成間に差がなく、あた
かも一つの物質のように挙動する組成物であり、蒸発、
凝縮を繰り返した後の組成物の組成に変化を生じないも
のである。一方、共沸様組成物とは、その気相組成と液
相組成が近似しており、発泡剤等に応用した場合、実用
上その組成が同一と見なせるものである。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The azeotropic and azeotropic composition-like compositions according to the present invention will be described in detail below. Note that an azeotropic composition is a composition that has no difference between the composition of a liquid phase and a composition of a gaseous phase under a constant pressure and behaves as if it were a single substance.
It does not change the composition of the composition after repeated condensation. On the other hand, the azeotropic composition has a gas phase composition and a liquid phase composition similar to each other, and when applied to a foaming agent or the like, the composition can be regarded as practically the same.

【0006】HFE−347pc−fが49から73重
量%及びシクロペンタンが51から27重量%からなる
組成物、好ましくはHFE−347pc−fが55から
68重量%及びシクロペンタンが45から32重量%か
らなる組成物は、これらの組成物の液相と気相の組成が
近似しており、実用上同一と見なせる共沸様組成物であ
る。より好ましくはHFE−347pc−fが63.1
から65.1重量%及びシクロペンタンが36.9から
34.9重量%、さらに好ましくはHFE−347pc
−fが64.07重量%及びシクロペンタンが35.9
3重量%である組成物は共沸組成物である。この共沸組
成物は最低共沸点であり、共沸温度は大気圧(760m
mHg)で38.12℃である。
A composition comprising 49 to 73% by weight of HFE-347pc-f and 51 to 27% by weight of cyclopentane, preferably 55 to 68% by weight of HFE-347pc-f and 45 to 32% by weight of cyclopentane. Are azeotropic compositions in which the compositions of the liquid phase and the gas phase of these compositions are similar and can be regarded as practically the same. More preferably, HFE-347pc-f is 63.1.
To 65.1% by weight and cyclopentane from 36.9 to 34.9% by weight, more preferably HFE-347pc
-F 64.07% by weight and cyclopentane 35.9
Compositions that are 3% by weight are azeotropic compositions. This azeotropic composition has the lowest azeotropic point and the azeotropic temperature is atmospheric pressure (760 m
38.12 ° C. in mHg).

【0007】また、HFE−347pc−fが38から
64重量%及びn−ペンタンが62から36重量%から
なる組成物好ましくはHFE−347pc−fが45か
ら58重量%及びn−ペンタンが55から42重量%か
らなる組成物は、これらの組成物の液相と気相の組成が
近似しており、実用上同一と見なせる共沸様組成物であ
る。より好ましくはHFE−347pc−fが49.5
から51.5重量%及びn−ペンタンが50.5から4
8.5重量%、さらに好ましくはHFE−347pc−
fが50.47重量%及びn−ペンタンが49.53重
量%である組成物は共沸組成物である。この共沸組成物
は最低共沸点であり、共沸温度は大気圧(760mmH
g)で30.87℃である。
A composition comprising 38 to 64% by weight of HFE-347pc-f and 62 to 36% by weight of n-pentane, preferably 45 to 58% by weight of HFE-347pc-f and 55 to 55% by weight of n-pentane. The compositions composed of 42% by weight are compositions in which the compositions of the liquid phase and the gas phase of these compositions are close to each other, and are azeotropic compositions which can be regarded as practically the same. More preferably, HFE-347pc-f is 49.5.
To 51.5% by weight and n-pentane is 50.5 to 4
8.5% by weight, more preferably HFE-347pc-
Compositions where f is 50.47% by weight and n-pentane is 49.53% by weight are azeotropic compositions. This azeotropic composition has a minimum azeotropic point and an azeotropic temperature at atmospheric pressure (760 mmH
g) is 30.87 ° C.

【0008】本発明で使用するHFEは公知の方法で容
易に合成可能である。合成例としては以下の方法が挙げ
られる。 HFE−347pc−f: CF2=CF2 + CF3CH2OH + KOH →
CHF2CF2OCH2CF3
[0008] The HFE used in the present invention can be easily synthesized by a known method. Examples of the synthesis include the following methods. HFE-347pc-f: CF 2 = CF 2 + CF 3 CH2OH + KOH →
CHF 2 CF 2 OCH 2 CF 3

【0009】本発明による組成物は、過酷な条件での使
用に際しては更に各種の安定剤を添加してもよい。この
ような安定剤の具体例を以下に例示する。1,2−ブチ
レンオキサイド、スチレンオキサイド、プロピレンオキ
サイド、2,6−ジ−t−ブチル−p−クレゾール、p
−t−ブチルフェノール、p−クレゾール、p−メトキ
シフェノール、t−ブチルカテコール、イソオイゲノー
ル、オイゲノール、チモール、ブチルヒドロキシアニソ
ール、プロパルギルアルコール、α−メチルスチレン、
アクリル酸エチル、アクリル酸メチル、アリルグリシジ
ルエーテル、イソプレン、グリシジルメタクリレート、
ジエチルグリコールモノメタクリレート、ビニルトルエ
ン、メタクリル酸メチル、1−ニトロプロパン、2−ニ
トロプロパン、ニトロエタン、ニトロベンゼン、ニトロ
メタン、2,5−ジ−t−アミルハイドロキノン、2,
5−ジ−t−ブチルハイドロキノン等。このほか、これ
らの化合物の同族体、誘導体も効果が期待できる。これ
らの安定剤は、単独で使用してもよくあるいは2種以上
組み合わせて使用してもよい。安定剤の使用量は、安定
剤の種類等により異なるが、その使用量は、通常本発明
組成物に対して0.005〜10重量%程度であり、
0.01〜5重量%程度とすることがより好ましい。
The composition according to the present invention may further contain various stabilizers when used under severe conditions. Specific examples of such a stabilizer are illustrated below. 1,2-butylene oxide, styrene oxide, propylene oxide, 2,6-di-t-butyl-p-cresol, p
-T-butylphenol, p-cresol, p-methoxyphenol, t-butylcatechol, isoeugenol, eugenol, thymol, butylhydroxyanisole, propargyl alcohol, α-methylstyrene,
Ethyl acrylate, methyl acrylate, allyl glycidyl ether, isoprene, glycidyl methacrylate,
Diethyl glycol monomethacrylate, vinyl toluene, methyl methacrylate, 1-nitropropane, 2-nitropropane, nitroethane, nitrobenzene, nitromethane, 2,5-di-t-amylhydroquinone, 2,
5-di-t-butylhydroquinone and the like. In addition, homologues and derivatives of these compounds can also be expected to have an effect. These stabilizers may be used alone or in combination of two or more. The amount of the stabilizer used varies depending on the type of the stabilizer and the like, but the amount used is usually about 0.005 to 10% by weight based on the composition of the present invention.
More preferably, it is about 0.01 to 5% by weight.

【0010】本発明組成物を溶剤、洗浄剤、反応溶媒、
塗料用溶剤,抽出剤、水切り剤、乾燥剤等の用途に使用
する場合、溶解力、洗浄力等をより一層改善するために
必要に応じて各種有機溶媒、界面活性剤等の添加剤を加
えることができる。有機溶媒としては公知のメタノー
ル、エタノール、2−プロパノール、塩化メチレン、
1,2−ジクロロエチレン等が挙げられ、その添加量は
通常1から20%、好ましくは2から10%が適切であ
る。界面活性剤としては、ソルビタンモノオレエ−ト,
ソルビタントリオレエ−ト等のソルビタン脂肪酸エステ
ル類、ポリオキシエチレンのソルビットテトラオレエ−
ト等のポリオキシエチレンソルビット脂肪酸エステル
類、ポリオキシエチレンモノラウレ−ト等のポリエチレ
ングリコ−ル脂肪酸エステル類、ポリオキシエチレンラ
ウリルエ−テル等のポリオキシエチレンアルキルエ−テ
ル類、ポリオキシエチレンノニルフェニルエ−テル等の
ポリオキシエチレンアルキルフェニルエ−テル類、ポリ
オキシエチレンオレイン酸アミド等のポリオキシエチレ
ンアルキルアミン脂肪酸アミド類等のノニオン系界面活
性剤が挙げられ、これらは単独で使用しても、あるいは
2種以上組み合わせて使用してもよい。相乗的に洗浄力
及び界面作用を改善する目的で、これらのノニオン系界
面活性剤に更にカチオン系界面活性剤又はアニオン系界
面活性剤を併用してもよい。界面活性剤の使用量は、そ
の種類等により異なるが、通常本発明組成物の0.1〜
20重量%程度であり、0.3〜5重量%程度とするこ
とがより好ましい。
[0010] The composition of the present invention comprises a solvent, a detergent, a reaction solvent,
When used for applications such as paint solvents, extractants, drainers, and desiccants, various organic solvents and additives such as surfactants are added as necessary to further improve the dissolving power and detergency. be able to. Known organic solvents include methanol, ethanol, 2-propanol, methylene chloride,
1,2-dichloroethylene and the like can be mentioned, and its addition amount is usually 1 to 20%, preferably 2 to 10%. Surfactants include sorbitan monooleate,
Sorbitan fatty acid esters such as sorbitan trioleate and sorbitan tetraoleate of polyoxyethylene
Polyoxyethylene sorbite fatty acid esters such as polyoxyethylene monolaurate, polyethylene glycol fatty acid esters such as polyoxyethylene monolaurate, polyoxyethylene alkyl ethers such as polyoxyethylene lauryl ether, polyoxyethylene Nonionic surfactants such as polyoxyethylene alkylphenyl ethers such as nonylphenyl ether, and polyoxyethylene alkylamine fatty acid amides such as polyoxyethylene oleic acid amide, and the like. Or a combination of two or more. For the purpose of synergistically improving the detergency and the interfacial action, a cationic surfactant or an anionic surfactant may be used in combination with these nonionic surfactants. The amount of the surfactant used varies depending on the type and the like, but is usually 0.1 to 10% of the composition of the present invention.
It is about 20% by weight, and more preferably about 0.3 to 5% by weight.

【0011】これらの組成物は特にフラックス洗浄剤,
洗浄溶剤,脱脂洗浄剤,水切り乾燥剤として好適であ
り、従来のフロン113や1,1,1−トリクロロエタ
ンの代替物として極めて有用なものである。その具体的
な用途としては、フラックス、グリ−ス、油、ワック
ス、インキ等の除去剤、電子部品(プリント基板、液晶
表示器、磁気記録部品、半導体材料等)、電機部品、精
密機械部品、樹脂加工部品、光学レンズ、衣料品等の洗
浄剤や水切り乾燥剤等を挙げることができる。その洗浄
方法としては、浸漬、スプレー、沸騰洗浄、超音波洗
浄、蒸気洗浄等若しくはこれらの組合せ等の従来から用
いられている方法が採用できる。
These compositions are, in particular, flux detergents,
It is suitable as a cleaning solvent, a degreasing cleaning agent, and a desiccant drying agent, and is extremely useful as a substitute for conventional Freon 113 and 1,1,1-trichloroethane. Specific applications include flux, grease, oil, wax, and ink removers, electronic components (printed circuit boards, liquid crystal displays, magnetic recording components, semiconductor materials, etc.), electrical components, precision machinery components, Examples include detergents for resin-processed parts, optical lenses, clothing, and the like, and drainers and desiccants. As the cleaning method, a conventionally used method such as immersion, spraying, boiling cleaning, ultrasonic cleaning, steam cleaning, or a combination thereof can be adopted.

【0012】本発明で得られた組成物はポリウレタンフ
ォームの発泡剤や断熱ガスとしても使用可能である。発
泡剤とポリオールとの相溶性はそれらの種類により、ケ
ースバイケースであるが、一般に、HFE単独の場合、
ポリオールとの相溶性が低い。しかし、複数のHFEを
混合することによって、相溶性が改善されることが多
い。本発明で得られた組成物は異種のHFEを混合して
いるので、HFE単独に比べて、ポリオールとの相溶性
が優れているが、本発明者らが既にこれ以前の出願で示
したようにポリオールとの相溶性を増すためにフッ素系
の界面活性剤を使用することも可能である。また、界面
活性剤の使用を好まない場合は発泡直前に本組成物をポ
リオール混合し、硬質ウレタンフォームを製造すること
も出来る。
The composition obtained in the present invention can also be used as a foaming agent for polyurethane foam or a heat insulating gas. The compatibility between the foaming agent and the polyol is case-by-case depending on their type, but generally, in the case of HFE alone,
Poor compatibility with polyol. However, compatibility is often improved by mixing multiple HFEs. Since the composition obtained in the present invention is a mixture of different types of HFE, it has better compatibility with the polyol than HFE alone, but as the present inventors have already shown in previous applications. It is also possible to use a fluorine-based surfactant to increase the compatibility with the polyol. If the use of a surfactant is not preferred, the composition may be mixed with a polyol immediately before foaming to produce a rigid urethane foam.

【0013】本発明の組成物を用いて硬質ウレタンフォ
ームの製造には、本組成物とポリオール、ポリイソシア
ネート、触媒、水、界面活性剤、整泡剤を混合、反応さ
せる。ポリイソシアネートには、芳香族、環状脂肪族、
鎖状脂肪族系のものが包含され、従来一般に使用されて
いる2官能のものが用いられる。このようなものとして
は、例えば、トリレンジイソシアネート、ジフェニルメ
タンジイソシアネート、ポリメチレンポリフェニルポリ
イソシアネート、トリジンジイソシアネート、ナフタリ
ンジイソシアネート、ヘキサメチレンジイソシアネー
ト、イソホロンジイソシアネート、キシリレンジイソシ
アネート、水添キシリレンジイソシアネート、ジシクロ
ヘキシルメタンジイソシアネート等が挙げられる。これ
らのものは単独又は混合物の形で用いられる。
In the production of a rigid urethane foam using the composition of the present invention, the composition, a polyol, a polyisocyanate, a catalyst, water, a surfactant and a foam stabilizer are mixed and reacted. Polyisocyanates include aromatic, cycloaliphatic,
A chain aliphatic type is included, and a bifunctional type generally used conventionally is used. As such, for example, tolylene diisocyanate, diphenylmethane diisocyanate, polymethylene polyphenyl polyisocyanate, tolidine diisocyanate, naphthalene diisocyanate, hexamethylene diisocyanate, isophorone diisocyanate, xylylene diisocyanate, hydrogenated xylylene diisocyanate, dicyclohexyl methane diisocyanate, etc. Is mentioned. These are used alone or in the form of a mixture.

【0014】ポリオールには、ポリエーテル系ポリオー
ル、ポリエステル系ポリオール、多価アルコール、水酸
基含有ジエチレン系ポリマー等が包含されるが、ポリエ
ーテル系ポリオールの使用が好ましい。また、ポリエー
テル系ポリオールを主成分とし、ポリエステル系ポリオ
ール等の他のポリオールを含むポリオールの使用も可能
である。ポリエーテル系ポリオールとしては、ポリプロ
ピレングリコール、ポリテトラメチレングリコール及び
それら変性体の他、糖、多価アルコール、アルカノール
アミン等の活性水素を含む化合物をイニシエータにし
て、これに、プロピレンオキシド、エチレンオキシド、
エピクロルヒドリン、ブチレンオキシド等の環状エーテ
ルを付加したものが好ましく使用される。ポリエステル
系ポリオールには、縮合系ポリエステルポリオール、ラ
クトン系ポリエステルポリオール、ポリカーボネートポ
リオール等が包含される。ポリオールとしては、通常、
その水酸基価が100〜1000のものが使用される。
The polyol includes a polyether-based polyol, a polyester-based polyol, a polyhydric alcohol, a hydroxyl group-containing diethylene-based polymer, and the like, and the use of a polyether-based polyol is preferred. It is also possible to use a polyol containing a polyether-based polyol as a main component and other polyols such as a polyester-based polyol. Examples of the polyether polyol include, in addition to polypropylene glycol, polytetramethylene glycol and modified products thereof, sugars, polyhydric alcohols, compounds containing active hydrogen such as alkanolamines as initiators, and propylene oxide, ethylene oxide,
Those to which cyclic ethers such as epichlorohydrin and butylene oxide are added are preferably used. The polyester-based polyol includes a condensation-based polyester polyol, a lactone-based polyester polyol, a polycarbonate polyol, and the like. As a polyol, usually
Those having a hydroxyl value of 100 to 1,000 are used.

【0015】触媒には、有機金属系触媒と有機アミン系
触媒が包含される。有機金属系触媒としては、有機スズ
化合物が好ましく使用され、スタナスオクトエート、ス
タナスラウレート、ジブチル錫ジラウレート、ジブチル
錫ジマレエート、ジブチル錫ジアセテート、ジオクチル
錫ジアセテート等が挙げられる。有機アミン系触媒とし
ては、第3級アミン、例えば、トリエチレンジアミン、
N−エチルモルホリン、トリエチルアミン、N,N,
N’,N’−テトラメチルヘキサメチレンジアミン、ビ
ス(2−ジメチルアミノエチル)エーテル、N,N’,
N’−トリエチルエタノールアミン等が挙げられる。
The catalyst includes an organometallic catalyst and an organic amine catalyst. As the organometallic catalyst, an organotin compound is preferably used, and examples thereof include stannasoctoate, stannaslaurate, dibutyltin dilaurate, dibutyltin dimaleate, dibutyltin diacetate, and dioctyltin diacetate. Examples of the organic amine catalyst include tertiary amines such as triethylenediamine,
N-ethylmorpholine, triethylamine, N, N,
N ′, N′-tetramethylhexamethylenediamine, bis (2-dimethylaminoethyl) ether, N, N ′,
N'-triethylethanolamine and the like.

【0016】本発明においては、前記したように、発泡
剤としての含フッ素エーテルの使用との関連で、界面活
性剤としてパーフルオロアルキル基を有する含フッ素界
面活性剤を用いる。本発明においては、発泡剤として使
用する組成物中の含フッ素エーテル化合物の表面張力が
低いので、含フッ素系界面活性剤を用いることによりポ
リオールに対する発泡剤の相溶性をコントロールするこ
とができる。含フッ素系界面活性剤の使用量は、発泡剤
100重量部当り、0.001〜10重量部、好ましく
は0.01〜5重量部の割合である。含フッ素系界面活
性剤としては、例えば、下記のものが挙げられる。 (1)RfSO2NR−(C24O)nH (2)RfSO2NR−CH2COOK (3)RfSO3M 前記式中、Rfはパーフルオロアルキル基を示し、Rは
アルキル基を示し、MはNH4、K又はNaを示し、n
は10〜2の数を示す。
In the present invention, as described above, a fluorine-containing surfactant having a perfluoroalkyl group is used as a surfactant in connection with the use of a fluorine-containing ether as a foaming agent. In the present invention, since the surface tension of the fluorinated ether compound in the composition used as the blowing agent is low, the compatibility of the blowing agent with the polyol can be controlled by using a fluorinated surfactant. The amount of the fluorinated surfactant is 0.001 to 10 parts by weight, preferably 0.01 to 5 parts by weight, per 100 parts by weight of the foaming agent. Examples of the fluorinated surfactant include the following. (1) RfSO 2 NR- (C 2 H 4 O) nH (2) RfSO 2 NR-CH 2 COOK (3) RfSO in 3 M wherein formula, Rf represents a perfluoroalkyl group, R represents an alkyl group , M represents NH 4 , K or Na, n
Indicates a number of 10 to 2.

【0017】本発明の発泡剤の使用割合は、ポリオール
100重量部当り、5〜50重量部、好ましくは15〜
30重量部であり、このような量の発泡剤の使用によ
り、20kg/m3以上、特に、30〜80kg/m3
密度を有する硬質ポリウレタンフォームを得ることがで
きる。原料混合物の反応温度は、15〜90℃、好まし
くは20〜60℃、より好ましくは20〜35℃であ
る。硬質ポリウレタンフォームの製造方法には、従来公
知の各種の方法が包含され、本発明における硬質ポリウ
レタンフォームは、ワンショット法やプレポリマー法で
製造することができる。また、そのフォームを得る際の
発泡方式としては、現場発泡、スラブ発泡、注入発泡
(充填法、モールド法)、ラミネート発泡、スプレー発
泡等の各種の発泡方式を採用することができる。
The proportion of the foaming agent of the present invention is 5 to 50 parts by weight, preferably 15 to 50 parts by weight, per 100 parts by weight of the polyol.
A 30 parts by weight, the use of such amount of blowing agent, 20 kg / m 3 or more, in particular, can be obtained a rigid polyurethane foam having a density of 30~80kg / m 3. The reaction temperature of the raw material mixture is 15 to 90C, preferably 20 to 60C, more preferably 20 to 35C. The method for producing the rigid polyurethane foam includes various conventionally known methods, and the rigid polyurethane foam in the present invention can be produced by a one-shot method or a prepolymer method. Further, as a foaming method for obtaining the foam, various foaming methods such as in-situ foaming, slab foaming, injection foaming (filling method, molding method), laminate foaming, and spray foaming can be adopted.

【0018】本組成物は前記発泡剤の用途の他、冷媒、
伝熱媒体、作動流体等にも使用可能である。
The present composition may be used in addition to the above-mentioned foaming agent, as well as a refrigerant,
It can also be used as a heat transfer medium, working fluid, and the like.

【0019】[0019]

【実施例】次に、本発明を実施例により更に詳細に説明
する。
Next, the present invention will be described in more detail with reference to examples.

【0020】実施例1 循環式気液平衡測定装置(容量35cc)で、試料とし
てHFE−347pc−fとシクロペンタンとの混合物
を用いて気液平衡組成及び沸点を測定した。HFE−3
47pc−fとシクロペンタンとの一定組成の混合試料
を試料容器部に入れ加熱した。そして気相凝縮液の滴下
速度が適正になるように加熱を調整して、安定した沸騰
を40分間以上保った。圧力及び沸点が安定しているこ
とを確かめた後、圧力、沸点を測定した。そして液相及
び気相凝縮液をサンプリングし、ガスクロマトグラフィ
−でサンプリング液の組成分析を行った。この結果を表
1に示す。前記実験結果から、HFE−347pc−f
が64.07重量%及びシクロペンタンが35.93重
量%からなる組成物は共沸組成物であり、その沸点は大
気圧(760mmHg)で38.12℃である。ここで
HFE−347pc−fが49から72重量%及びシク
ロペンタンが51から27重量%の範囲にある本発明の
組成物は気相と液相の組成が10%以内であり、HFE
−347pc−fが55から68重量%及びシクロペン
タンが45から32重量%の範囲にある本発明の組成物
は気相と液相の組成が5%以内であり、実用上同一組成
と見なせる共沸様組成物である。
Example 1 A gas-liquid equilibrium composition and a boiling point were measured using a mixture of HFE-347pc-f and cyclopentane as a sample with a circulation-type gas-liquid equilibrium measuring apparatus (capacity: 35 cc). HFE-3
A mixed sample having a constant composition of 47 pc-f and cyclopentane was placed in a sample container and heated. The heating was adjusted so that the dropping rate of the vapor-phase condensate became appropriate, and stable boiling was maintained for 40 minutes or more. After confirming that the pressure and the boiling point were stable, the pressure and the boiling point were measured. The liquid phase and the gas phase condensate were sampled, and the composition of the sampled solution was analyzed by gas chromatography. Table 1 shows the results. From the above experimental results, HFE-347pc-f
Is 64.07% by weight and 35.93% by weight of cyclopentane is an azeotropic composition having a boiling point of 38.12 ° C. at atmospheric pressure (760 mmHg). Here, the composition of the present invention having HFE-347pc-f in the range of 49 to 72% by weight and cyclopentane in the range of 51 to 27% by weight has a composition of the gas phase and the liquid phase within 10%, and the HFE
The composition of the present invention having -347 pc-f in the range of 55 to 68% by weight and cyclopentane in the range of 45 to 32% by weight has a composition of the gaseous phase and the liquid phase of 5% or less. It is a boiling-like composition.

【0021】実施例2 シクロペンタンの代わりに、n−ペンタンを用いた以外
は実施例1と同様にして、実験を行った。その結果を表
2に示す。
Example 2 An experiment was conducted in the same manner as in Example 1 except that n-pentane was used instead of cyclopentane. Table 2 shows the results.

【0022】[0022]

【表1】 [Table 1]

【0023】[0023]

【表2】 [Table 2]

【0024】[0024]

【発明の効果】本発明の組成物は、地球環境への影響を
小さく、かつ性能の高いCFC、HCFCの代替物とし
て有利に使用される。
Industrial Applicability The composition of the present invention is advantageously used as a substitute for CFC and HCFC which has little effect on the global environment and has high performance.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 高田 直門 東京都文京区本郷2−40−17本郷若井ビ ル6階 財団法人地球環境産業技術研究 機構 新規冷媒等プロジェクト室内 (72)発明者 山本 博志 東京都文京区本郷2−40−17本郷若井ビ ル6階 財団法人地球環境産業技術研究 機構 新規冷媒等プロジェクト室内 (72)発明者 関屋 章 茨城県つくば市東1丁目1番 工業技術 院物質工学工業技術研究所内 審査官 藤森 知郎 (58)調査した分野(Int.Cl.6,DB名) C07C 43/12 CA(STN) CAOLD(STN) REGISTRY(STN)──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor, Namon Takada 6th floor, Hongo Wakai Building, Hongo 2-40-17, Hongo, Bunkyo-ku, Tokyo Project for New Refrigerants, etc. (72) Hiroshi Yamamoto, Inventor 6-floor Hongo Wakai Building, Hongo 2-40-17, Bunkyo-ku, Tokyo New Research Project Room for New Refrigerants, etc. (72) Inventor Akira Sekiya 1-1-1, Higashi, Tsukuba, Ibaraki Pref. Toshiro Fujimori, Examiner in the Technical Research Institute (58) Field surveyed (Int. Cl. 6 , DB name) C07C 43/12 CA (STN) CAOLD (STN) REGISTRY (STN)

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 ヒドロフルオロエーテルのコードをHF
E−347pc−f:CHF2CF2OCH2CF3と定義
したとき、HFE−347pc−fとシクロペンタンか
らなる共沸組成物または共沸様組成物。
1. The hydrofluoroether code is HF
E-347pc-f: An azeotropic composition or an azeotrope-like composition composed of HFE-347pc-f and cyclopentane when defined as CHF 2 CF 2 OCH 2 CF 3 .
【請求項2】 ヒドロフルオロエーテルのコードをHF
E−347pc−f:CHF2CF2OCH2CF3と定義
したとき、HFE−347pc−fとn−ペンタンから
なる共沸組成物または共沸様組成物。
2. The hydrofluoroether code is HF
E-347pc-f: An azeotropic composition or an azeotropic composition composed of HFE-347pc-f and n-pentane when defined as CHF 2 CF 2 OCH 2 CF 3 .
JP10188302A 1998-06-18 1998-06-18 Azeotropic composition and azeotrope-like composition containing 2,2,1,1-tetrafluoroethyl 2 ', 2', 2'-trifluoroethyl ether Expired - Lifetime JP2955598B1 (en)

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EP1808481B1 (en) * 2004-10-05 2008-10-08 Asahi Glass Company, Limited Azeotrope-like solvent composition and mixed solvent composition
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