JPS5811035A - Stabilizing method for absorption type refrigerant composition - Google Patents
Stabilizing method for absorption type refrigerant compositionInfo
- Publication number
- JPS5811035A JPS5811035A JP10884281A JP10884281A JPS5811035A JP S5811035 A JPS5811035 A JP S5811035A JP 10884281 A JP10884281 A JP 10884281A JP 10884281 A JP10884281 A JP 10884281A JP S5811035 A JPS5811035 A JP S5811035A
- Authority
- JP
- Japan
- Prior art keywords
- absorption
- refrigerant composition
- tetraethylene glycol
- refrigerant
- epoxides
- 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.)
- Granted
Links
- 239000003507 refrigerant Substances 0.000 title claims abstract description 26
- 238000010521 absorption reaction Methods 0.000 title claims abstract description 25
- 238000000034 method Methods 0.000 title claims description 12
- 239000000203 mixture Substances 0.000 title claims description 11
- 230000000087 stabilizing effect Effects 0.000 title claims description 6
- ZUHZGEOKBKGPSW-UHFFFAOYSA-N tetraglyme Chemical compound COCCOCCOCCOCCOC ZUHZGEOKBKGPSW-UHFFFAOYSA-N 0.000 claims abstract description 24
- 150000002118 epoxides Chemical class 0.000 claims abstract description 13
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 3
- 150000002989 phenols Chemical class 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 abstract description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 8
- 229910052751 metal Inorganic materials 0.000 abstract description 5
- 239000002184 metal Substances 0.000 abstract description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract description 4
- 229910052802 copper Inorganic materials 0.000 abstract description 4
- 239000010949 copper Substances 0.000 abstract description 4
- 229910052742 iron Inorganic materials 0.000 abstract description 4
- 150000002739 metals Chemical class 0.000 abstract description 4
- 239000000463 material Substances 0.000 abstract description 3
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 abstract 1
- 229940029284 trichlorofluoromethane Drugs 0.000 abstract 1
- 239000002250 absorbent Substances 0.000 description 10
- 230000002745 absorbent Effects 0.000 description 10
- 230000006835 compression Effects 0.000 description 6
- 238000007906 compression Methods 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 6
- 238000012360 testing method Methods 0.000 description 5
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 4
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 239000006096 absorbing agent Substances 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 238000005057 refrigeration Methods 0.000 description 3
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 2
- JIGUICYYOYEXFS-UHFFFAOYSA-N 3-tert-butylbenzene-1,2-diol Chemical compound CC(C)(C)C1=CC=CC(O)=C1O JIGUICYYOYEXFS-UHFFFAOYSA-N 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 2
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 2
- 239000005770 Eugenol Substances 0.000 description 2
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 2
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 2
- 229960002217 eugenol Drugs 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
- BOSAWIQFTJIYIS-UHFFFAOYSA-N 1,1,1-trichloro-2,2,2-trifluoroethane Chemical compound FC(F)(F)C(Cl)(Cl)Cl BOSAWIQFTJIYIS-UHFFFAOYSA-N 0.000 description 1
- RFCAUADVODFSLZ-UHFFFAOYSA-N 1-Chloro-1,1,2,2,2-pentafluoroethane Chemical compound FC(F)(F)C(F)(F)Cl RFCAUADVODFSLZ-UHFFFAOYSA-N 0.000 description 1
- PQXKWPLDPFFDJP-UHFFFAOYSA-N 2,3-dimethyloxirane Chemical compound CC1OC1C PQXKWPLDPFFDJP-UHFFFAOYSA-N 0.000 description 1
- YSUQLAYJZDEMOT-UHFFFAOYSA-N 2-(butoxymethyl)oxirane Chemical compound CCCCOCC1CO1 YSUQLAYJZDEMOT-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- 239000004340 Chloropentafluoroethane Substances 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- 239000004341 Octafluorocyclobutane Substances 0.000 description 1
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
- 238000010793 Steam injection (oil industry) Methods 0.000 description 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
- 239000005844 Thymol Substances 0.000 description 1
- 230000009102 absorption Effects 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical group F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 235000019406 chloropentafluoroethane Nutrition 0.000 description 1
- AFYPFACVUDMOHA-UHFFFAOYSA-N chlorotrifluoromethane Chemical compound FC(F)(F)Cl AFYPFACVUDMOHA-UHFFFAOYSA-N 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- UMNKXPULIDJLSU-UHFFFAOYSA-N dichlorofluoromethane Chemical compound FC(Cl)Cl UMNKXPULIDJLSU-UHFFFAOYSA-N 0.000 description 1
- 229940099364 dichlorofluoromethane Drugs 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical compound FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 description 1
- 235000019407 octafluorocyclobutane Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 150000003902 salicylic acid esters Chemical class 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 1
Landscapes
- Sorption Type Refrigeration Machines (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、低級脂肪族塩素化弗素化炭化水素(以下フロ
ンという。)及びテトラエチレングリコールジメチルエ
ーテルからなる吸収冷媒組成物の安定化方法に関するも
のである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for stabilizing an absorption refrigerant composition comprising a lower aliphatic chlorinated fluorinated hydrocarbon (hereinafter referred to as fluorocarbon) and tetraethylene glycol dimethyl ether.
冷凍機Kt−t、、犬別して圧縮式、吸収式、蒸気噴射
式、吸着式があυ、そのうち圧縮式と吸収式が工業的規
模で広く用いられている。圧縮式冷凍機では、冷媒が蒸
発、圧縮、凝縮、膨張という循環を経るととKより冷凍
を行ない、吸収式冷凍機では蒸発、吸収、再生、凝縮と
いう循環によシ冷凍を行なっている。冷媒としては、毒
性が少なく、不燃性で金属等に対して不活性であること
から、ジクロロジフルオロメタンやクロロジフルオロメ
タン等各種のフロンが使われている。吸収式冷凍機にお
いては、冷媒がフロンの場合その吸収剤としては、テト
ラエチレングリコールジメチルエーテル等の有機済剤が
一般に用いられている。Refrigerators are classified into compression type, absorption type, steam injection type, and adsorption type, among which compression type and absorption type are widely used on an industrial scale. In a compression type refrigerator, the refrigerant undergoes a cycle of evaporation, compression, condensation, and expansion and then undergoes refrigeration, while in an absorption type refrigerator, refrigeration is performed by a cycle of evaporation, absorption, regeneration, and condensation. Various types of fluorocarbons, such as dichlorodifluoromethane and chlorodifluoromethane, are used as refrigerants because they are less toxic, nonflammable, and inert to metals. In absorption refrigerators, when the refrigerant is chlorofluorocarbon, an organic absorbent such as tetraethylene glycol dimethyl ether is generally used as the absorbent.
本発明者等の最近の検討によれば、圧縮式冷凍機では考
えられなかったフロンの分解が、吸収剤としてテトラエ
チレングリコールジメチルエーテルを用いた吸収式冷凍
機においては起っていることがわかった。その後、さら
に検討した結果、圧縮式と吸収式では冷媒循環時の最高
温度がかなり相違すること、及び吸収式では吸収剤の影
響があること、従ってかがる条件下では、金属に対して
不活性のフロンも、冷凍装置材質として使われている鉄
、銅あるいはアルミニウム等の影響を受けて不安定にな
ることを見い出すことができた。本発明者等は、吸収冷
凍機内の吸収剤及び金2属の共存下さらには、高温時に
おけるフロン冷媒の安定化とはかるべく、種々検討を積
み重ねた結果、エポキサイド類の添加が効果があること
を見い出すことができた。According to recent studies by the present inventors, it has been found that decomposition of fluorocarbons, which was unthinkable in compression refrigerators, occurs in absorption refrigerators that use tetraethylene glycol dimethyl ether as an absorbent. . After further investigation, we found that the maximum temperature during refrigerant circulation is quite different between the compression type and the absorption type, and that the absorption type is affected by the absorbent. It was discovered that even active fluorocarbons become unstable due to the influence of iron, copper, aluminum, etc. used as materials for refrigeration equipment. The inventors of the present invention have conducted various studies to stabilize the fluorocarbon refrigerant under the coexistence of the absorbent and metal metals in the absorption refrigerator and at high temperatures, and have found that the addition of epoxides is effective. I was able to find out.
すなわち本発明方法は、フロン及びテトラエチレングリ
コールジメチルエーテルからなる吸収冷媒組成物にエポ
キサイド類を添加することを特徴とする吸収冷媒組成物
の安定化方法に関するものである。さらに検討を積み重
ねた結果、エポキサイド類とフェノール類の組み合せが
上記目的を達成するためにさらに効果的であることを見
い出すことができた。That is, the method of the present invention relates to a method for stabilizing an absorption refrigerant composition, which is characterized by adding epoxides to an absorption refrigerant composition consisting of fluorocarbons and tetraethylene glycol dimethyl ether. As a result of further studies, it was discovered that a combination of epoxides and phenols is more effective in achieving the above objective.
すなわち本発明方法は、フロン及びテトラエチレングリ
コールジメチルエーテルからなる吸収冷媒組成物にエポ
キサイド類及びフェノール類を添加することを特徴とす
る吸収冷媒組成物の安定化方法をあわせて提供するもの
である。That is, the method of the present invention also provides a method for stabilizing an absorption refrigerant composition, which is characterized by adding epoxides and phenols to an absorption refrigerant composition consisting of fluorocarbons and tetraethylene glycol dimethyl ether.
安定化されるフロンとしては、冷媒として通常使用され
る低級脂肪族塩素化弗素化炭化水素で1.!l)、
)ジクロロフルオロメタン、ジクロロジフルオロメタン
、クロロトリフルオロメタン、クロロジフルオロメタン
、トリクロロトリフルオロエタン、オクタフルオロシク
ロブタン等するいは、クロロジフルオロメタンとクロロ
ペンタフルオロエタン等の各種共沸組成物があげられる
。クロロジフルオロメタン等が吸収冷媒として通常よく
使われている。かかるフロンを吸収する有機溶剤いわゆ
る吸収剤としては、吸収器ではフロンを多量に吸収し、
再生器ではフロンを多量に放出するような、吸収器と再
生器の作動条件差でフロンの溶解度が大きく変化するよ
うなもの、通常はテトラエチレングリコールジメチルエ
ーテルが好適に用いられる。The stabilized fluorocarbons include lower aliphatic chlorinated fluorinated hydrocarbons commonly used as refrigerants. ! l),
) dichlorofluoromethane, dichlorodifluoromethane, chlorotrifluoromethane, chlorodifluoromethane, trichlorotrifluoroethane, octafluorocyclobutane, and various azeotropic compositions such as chlorodifluoromethane and chloropentafluoroethane. Chlorodifluoromethane and the like are commonly used as absorption refrigerants. Organic solvents that absorb such fluorocarbons, so-called absorbers, absorb a large amount of fluorocarbons in absorbers.
For the regenerator, it is preferable to use a material that releases a large amount of fluorocarbons and whose solubility changes greatly depending on the operating conditions between the absorber and the regenerator, usually tetraethylene glycol dimethyl ether.
下記第1表には、温度170℃で吸収剤テトラエチレン
グリコールジメチルエーテルと鉄、銅及びアルミニウム
共存下の冷媒クロロジフルオロメタンの安定性を示した
。吸収剤が存在しない場合には、フロンの分解はほとん
ど起こらず、フロンが分解して発生するHOA +HF
の検出量はそれぞれ3 ppm以下、1 ppm以
下と微量である。ところが、吸収剤が存在するとフロン
の分解が激しくなることがわかる。本発明方法により、
エポキサイド類として1,2−ブチレンオキサイドを添
加することによ如、あるいはさらにフェノール類として
2.6−ジーt−ブチル−P−クレゾールを合わせて添
加することにより分解を抑えることができた。エポキサ
イド類としては7分子内に少なくとも1つの隣接エボレ
ンオキサイド、2.3−ブチレンオキサイド。Table 1 below shows the stability of the refrigerant chlorodifluoromethane in the presence of the absorbent tetraethylene glycol dimethyl ether and iron, copper, and aluminum at a temperature of 170°C. In the absence of an absorbent, almost no decomposition of fluorocarbons occurs, and HOA + HF is generated by the decomposition of fluorocarbons.
The detected amounts of these are very small, less than 3 ppm and less than 1 ppm, respectively. However, it can be seen that the presence of an absorbent intensifies the decomposition of fluorocarbons. By the method of the present invention,
Decomposition could be suppressed by adding 1,2-butylene oxide as an epoxide, or by further adding 2,6-di-t-butyl-P-cresol as a phenol. Epoxides include at least one adjacent evolene oxide and 2,3-butylene oxide in seven molecules.
エピクロルヒドリン、スチレンオキサイド、ブチルグリ
シジルエーテル&フェニルグリシジルエーテル、グリシ
ドール等が好ましい。特に好ましいエポキサイド類とし
ては、1.2−ブチレンオキサイドである。かかるエポ
キサイド類の添加量は、広範囲にわたって変更可能であ
るが、通常は冷媒フロンに対して0.01〜五〇重量%
程度が採用され、好ましくは005〜10重量%である
。フェノール類としては、フェノール、クレゾール、ブ
チルフェノール、チモール、2゜6−ジーt−ブチル−
p−クレゾール、オイゲノール、インオイゲノール、θ
−メトキシフェノール、p−メトキシフェノール、カテ
コール。Epichlorohydrin, styrene oxide, butyl glycidyl ether & phenyl glycidyl ether, glycidol, etc. are preferred. A particularly preferred epoxide is 1,2-butylene oxide. The amount of such epoxides added can vary over a wide range, but is usually 0.01 to 50% by weight based on the refrigerant Freon.
The amount is preferably between 0.005 and 10% by weight. Phenols include phenol, cresol, butylphenol, thymol, 2゜6-di-t-butyl-
p-cresol, eugenol, ineugenol, θ
-Methoxyphenol, p-methoxyphenol, catechol.
t−ブチルカテコール、サリチル酸エステル類、ビスフ
ェノールAあるいはその他のフェノール誘導体があるが
、好ましくはθ−メトキシフェノール、オイゲノール、
t−ブチルカテコール、2.6−ジーt−ブチル−p−
クレゾール等である。添加量は、広範囲にわたって変更
可能であるが、通常は冷媒フロンに対してn、005〜
!1.0重量%程度が採用され、好ましくはn、o1〜
1.0重t%が採用される。かかる安定剤は。Examples include t-butylcatechol, salicylic acid esters, bisphenol A or other phenol derivatives, preferably θ-methoxyphenol, eugenol,
t-butylcatechol, 2,6-di-t-butyl-p-
Cresol etc. Although the amount added can vary over a wide range, it is usually n, 005 to 005 for the refrigerant Freon.
! About 1.0% by weight is adopted, preferably n, o1~
1.0 weight t% is adopted. Such stabilizers.
本発明の目的を阻害しないかぎ、!71エポキサイド類
として2種以上、フェノール類として2種以上使用する
ことができる。The key is not to impede the purpose of the invention! Two or more types of 71 epoxides and two or more types of phenols can be used.
次に、本発明の実施例について更に具体的に説明するが
、かかる説明によって本発明が何ら限定されるものでな
いことは勿論である。Next, embodiments of the present invention will be described in more detail, but it goes without saying that the present invention is not limited by such explanations.
〈冷媒の安定性試験〉
1−1 試験装置
・試験容器 8US 516製耐圧容器内容積100
−1耐圧度100
b/car” G
・恒温槽 熱風強制循環式、精度170℃±1℃
1−2 試験条件
・温 度 170℃
・期 間 7日
・冷 媒 フロン22(クロロジフルオロメタン)
・吸収剤 テトラエチレングリコールジメチルエー
テル
・冷媒:吸収剤添加量 50r:50F・共存金属
鉄、銅、アルミニウム(25X 50 X rL
5 tax )
・安定剤 1.2−ブチレンオキサイド又は、1.2
−ブチレンオキサイド/2゜
6−ジーt−ブチル−p−フレ
ゾール
上記試験装置及び条件において、アルフッノン吸光4度
法によシHFを、A g、 N 01 比濁法によj
) HOjを測定し、フロン22の分解程度を推定した
。下記第1表にかかる試験結果茫示す。<Refrigerant stability test> 1-1 Test equipment/test container 8US 516 pressure container internal volume 100
-1 Pressure resistance 100 b/car” G ・Thermostatic chamber Hot air forced circulation type, accuracy 170℃±1℃ 1-2 Test conditions/Temperature 170℃ ・Duration 7 days ・Refrigerant Freon 22 (chlorodifluoromethane) ・Absorbent Tetraethylene glycol dimethyl ether Refrigerant: Absorbent addition amount 50r:50F Coexisting metals Iron, copper, aluminum (25X 50X rL
5 tax) ・Stabilizer 1.2-butylene oxide or 1.2
-Butylene oxide/2゜6-di-t-butyl-p-fresol Under the above test equipment and conditions, HF was measured by the Alfluorone absorption 4 degree method, A g, N 01 was measured by the nephelometric method.
) HOj was measured and the degree of decomposition of Freon 22 was estimated. The test results are shown in Table 1 below.
第 1 表Table 1
Claims (1)
ングリコールジメチルエーテルからなる吸収冷媒組成物
にエポキサイド類を添加することを特徴とする吸収冷媒
組成物の安定化方法。 2)低級脂肪族塩素化弗素化炭化水素及びテトラエチレ
ンクリコールジメチルエーテルカラなる吸収冷媒組成物
にエポキサイド類及びフェノール類?添加することを特
徴とする吸収冷媒組成物の安定化方法。[Scope of Claims] 1) A method for stabilizing an absorption refrigerant composition, which comprises adding epoxides to an absorption refrigerant composition comprising a lower aliphatic chlorinated fluorinated hydrocarbon and tetraethylene glycol dimethyl ether. 2) Epoxides and phenols in an absorption refrigerant composition consisting of lower aliphatic chlorinated fluorinated hydrocarbons and tetraethylene glycol dimethyl ether color? 1. A method for stabilizing an absorption refrigerant composition, the method comprising:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10884281A JPS5811035A (en) | 1981-07-14 | 1981-07-14 | Stabilizing method for absorption type refrigerant composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10884281A JPS5811035A (en) | 1981-07-14 | 1981-07-14 | Stabilizing method for absorption type refrigerant composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5811035A true JPS5811035A (en) | 1983-01-21 |
JPS636260B2 JPS636260B2 (en) | 1988-02-09 |
Family
ID=14494951
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10884281A Granted JPS5811035A (en) | 1981-07-14 | 1981-07-14 | Stabilizing method for absorption type refrigerant composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5811035A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4612133A (en) * | 1984-07-06 | 1986-09-16 | Atochem | Stable mixtures of chlorofluorocarbons and solvents and their use as heat transfer fluids |
WO1992017559A1 (en) * | 1991-04-05 | 1992-10-15 | Allied-Signal Inc. | Stabilized dichlorotrifluoroethane refrigeration compositions |
WO1992017563A1 (en) * | 1991-04-08 | 1992-10-15 | Allied-Signal Inc. | Stabilized polyoxyalkylene glycols |
WO1992017560A1 (en) * | 1991-04-05 | 1992-10-15 | Allied-Signal Inc. | Stabilized chlorine-containing refrigeration compositions |
-
1981
- 1981-07-14 JP JP10884281A patent/JPS5811035A/en active Granted
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4612133A (en) * | 1984-07-06 | 1986-09-16 | Atochem | Stable mixtures of chlorofluorocarbons and solvents and their use as heat transfer fluids |
WO1992017559A1 (en) * | 1991-04-05 | 1992-10-15 | Allied-Signal Inc. | Stabilized dichlorotrifluoroethane refrigeration compositions |
WO1992017560A1 (en) * | 1991-04-05 | 1992-10-15 | Allied-Signal Inc. | Stabilized chlorine-containing refrigeration compositions |
US5454966A (en) * | 1991-04-05 | 1995-10-03 | Alliedsignal Inc. | Stabilized chlorine-containing refrigeration compositions |
WO1992017563A1 (en) * | 1991-04-08 | 1992-10-15 | Allied-Signal Inc. | Stabilized polyoxyalkylene glycols |
Also Published As
Publication number | Publication date |
---|---|
JPS636260B2 (en) | 1988-02-09 |
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