JPH05156062A - Method for stabilizing halogenated hydrocarbon - Google Patents

Method for stabilizing halogenated hydrocarbon

Info

Publication number
JPH05156062A
JPH05156062A JP3320797A JP32079791A JPH05156062A JP H05156062 A JPH05156062 A JP H05156062A JP 3320797 A JP3320797 A JP 3320797A JP 32079791 A JP32079791 A JP 32079791A JP H05156062 A JPH05156062 A JP H05156062A
Authority
JP
Japan
Prior art keywords
halogenated hydrocarbon
blowing agent
premix
urethane foam
producing
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.)
Pending
Application number
JP3320797A
Other languages
Japanese (ja)
Inventor
Yasuo Hibino
泰雄 日比野
Hiroshi Hanamoto
博司 花本
Ryoichi Tamai
良一 玉井
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Central Glass Co Ltd
Original Assignee
Central Glass Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Central Glass Co Ltd filed Critical Central Glass Co Ltd
Priority to JP3320797A priority Critical patent/JPH05156062A/en
Publication of JPH05156062A publication Critical patent/JPH05156062A/en
Pending legal-status Critical Current

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  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

PURPOSE:To improve the storage stability of a premixed for producing a urethane foam, comprising a hydrochlorofluorocarbon as a blowing agent by adding a metallocene or a metal acetylacetone complex, etc., to a halogenated hydrocarbon. CONSTITUTION:An amine-based polyol such as N,N,N',N'-tetrakis(2- hydroxypropyl) ethylenediamine is blended with dimethylcyclohexylamine, water, a foam stabilizer and a halogenated hydrocarbon such as 1,1-dichloro-l- fluoroethane as a blowing agent to give a premix for producing a urethane foam, which is mixed with 0.1 pt.wt., based on the blowing agent, of one or more among metallocenes (e.g. ferrocene) and metal acetylacetone complexes [e.g. acetylacetanotomanganese (2)] as stabilizes for the blowing agent to improve the storage stability of the premix for producing urethane foam mixed with the hydrochlorofluorocarbon as the blowing agent.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明はフッ素およびその他のハ
ロゲンを含む炭素数2以上の低級脂肪族ハロゲン化炭化
水素の安定化に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to stabilization of lower aliphatic halogenated hydrocarbons having 2 or more carbon atoms containing fluorine and other halogens.

【0002】[0002]

【従来技術とその解決しようとする課題】一般にフッ素
および塩素を含むハロゲン化炭化水素は、水酸基を含む
アルコール類と水素交換反応を行ない、塩化水素等を発
生することが知られている。
2. Description of the Related Art It is generally known that halogenated hydrocarbons containing fluorine and chlorine undergo hydrogen exchange reaction with alcohols containing hydroxyl groups to generate hydrogen chloride and the like.

【0003】炭素数2以上のハロゲン化炭化水素を発泡
剤として硬質ウレタンフォーム発泡に用いる場合、プレ
ミックス組成としてポリオールとハロゲン化炭化水素と
が塩基触媒の存在下に接触するため上記の反応に加え、
ハロゲン化水素の脱離をともなったオレフィン生成反応
も併発することが予想される。
When a halogenated hydrocarbon having 2 or more carbon atoms is used as a foaming agent for foaming a rigid urethane foam, a polyol and a halogenated hydrocarbon are brought into contact with each other in the presence of a base catalyst as a premix composition, and therefore, in addition to the above reaction. ,
It is expected that an olefin production reaction accompanied by elimination of hydrogen halide will also occur.

【0004】従来、硬質ウレタンフォーム発泡に用いら
れてきたトリクロロフルオロメタン(CFC−11)
は、プレミックスの状態でポリオールのようなアルコー
ル性水酸基含有化合物と共存すると反応し、塩化水素、
アルデヒドその他分解生成物が生ずることから、ポリオ
ールの着色、粘度上昇、触媒劣化、容器腐食さらにはポ
リウレタンの性能低下をきたすことが懸念されてきた。
かかる問題点を回避するためCFC−11の分解を抑制
するために、種々の添加剤が発見され、実用化されてい
る。
Trichlorofluoromethane (CFC-11), which has been conventionally used for foaming rigid urethane foam
Reacts with an alcoholic hydroxyl group-containing compound such as a polyol in a premixed state, reacts with hydrogen chloride,
Since aldehydes and other decomposition products are generated, it has been feared that the polyol may be colored, the viscosity may be increased, the catalyst may be deteriorated, the container may be corroded, and the performance of the polyurethane may be deteriorated.
In order to avoid such problems, various additives have been discovered and put to practical use in order to suppress the decomposition of CFC-11.

【0005】たとえばαーメチルスチレン(特公昭39
ー23099)、pーイソプロペニルトルエン(特公昭
47ー625) 、ビニルトルエン(特開昭49ー718
8)、ビニルトルエンとニトロソベンゼン、pージオキ
サンまたはtーブチルピロカテコール等との組合せ(特
開昭53ー82708)、ビニルトルエンとアルキレン
オキシドとの組合せ(特開昭53ー82709)、イソ
オイゲノール、メトキシスチレンまたはエトキシスチレ
ン(特開昭53ー82710)、αーメチルスチレン誘
導体とフェノール類との組合せ(特公平1ー2572
6)、αーメチルスチレン誘導体、フェノール類とエポ
キシ化合物との組合せ(特公平1ー24771)等が安
定剤として提案されている。
For example, α-methylstyrene (Japanese Patent Publication Sho-39)
-23099), p-isopropenyltoluene (JP-B-47-625), vinyltoluene (JP-A-49-718).
8), a combination of vinyltoluene and nitrosobenzene, p-dioxane, t-butylpyrocatechol and the like (JP-A-53-82708), a combination of vinyltoluene and an alkylene oxide (JP-A-53-82709), isoeugenol, Combination of methoxystyrene or ethoxystyrene (JP-A-53-82710), α-methylstyrene derivative and phenols (Japanese Patent Publication No. 1-2572).
6), α-methylstyrene derivatives, combinations of phenols and epoxy compounds (Japanese Patent Publication No. 1-24771), etc. are proposed as stabilizers.

【0006】しかしながら、これらの安定剤はハロゲン
化炭化水素とアルコール性水酸基含有化合物との反応を
抑制することには有効であるものの、1,1−ジクロロ
ー1ーフルオロエタンのようなハロゲン化炭化水素にお
けるハロゲン化水素の脱離をともなうオレフィン生成反
応の抑制には充分な効果を示さないという問題点があっ
た。
However, although these stabilizers are effective in suppressing the reaction between the halogenated hydrocarbon and the compound containing an alcoholic hydroxyl group, halogens in the halogenated hydrocarbon such as 1,1-dichloro-1-fluoroethane are not effective. There is a problem that it does not show a sufficient effect in suppressing the olefin formation reaction accompanied by desorption of hydrogen fluoride.

【0007】[0007]

【課題を解決しようとする具体的な手段】本発明者ら
は、硬質ウレタンフォームのプレミックスの貯蔵安定性
を改善すること、特に、ハロゲン化炭化水素におけるハ
ロゲン化水素の脱離をともなうオレフィン生成反応の抑
制を図ることを目的に鋭意検討を加えた結果、かかる安
定化効果の知られていなかったメタロセンおよび金属ア
セチルアセトン錯体などの有機金属化合物が分解反応の
抑制に有効であるという事実を見出し、本発明に到った
ものである。
The present inventors have improved the storage stability of rigid urethane foam premixes and, in particular, olefin formation with elimination of hydrogen halide in halogenated hydrocarbons. As a result of diligent studies aimed at suppressing the reaction, the fact that organometallic compounds such as metallocene and metal acetylacetone complex, whose stabilizing effect was not known, is effective in suppressing the decomposition reaction, was found. The present invention has been reached.

【0008】すなわち、ハロゲン化炭化水素にメタロセ
ン類または金属アセチルアセトン錯体から選ばれる1種
以上を添加することを特徴とするハロゲン化炭化水素の
安定化方法である。
That is, the method for stabilizing a halogenated hydrocarbon is characterized by adding at least one selected from metallocenes and metal acetylacetone complexes to the halogenated hydrocarbon.

【0009】本発明において用いられるメタロセン類と
しては、Fe、Ti、V、Cr、Mn、Co、Ni、M
o、Ru、Rh、Lu、Ta、W、Os、Irなどとシ
クロペンタジエニルよりなる錯塩が挙げられるが、フェ
ロセン、ニッケロセン、 コバルトセン、 二塩化モリブド
セン、二塩化ジシクロペンタジエニルチタニウム、二塩
化ジシクロペンタジエニルジルコニウム等が好ましく、
また、本発明において用いられる金属アセチルアセトン
錯体類としては、Li、Na、K、Ag、Au、Tl、
Au、Ga、Co、Cu、Be、Mg、Zn、Cd、H
g、Pb、Mo、Ni、B、Ca、Sr、Ba、Pd、
Pt、In、Se、Ce、Ta、La、Ti、Mn、F
e、Cr、V、Si、Zrとアセチルアセトンの錯塩が
挙げられるが、マンガン(2)アセチルアセトネート、
コバルト(2)アセチルアセトネート等が好ましい。
The metallocenes used in the present invention include Fe, Ti, V, Cr, Mn, Co, Ni and M.
Examples thereof include complex salts of cyclopentadienyl with o, Ru, Rh, Lu, Ta, W, Os, Ir and the like. Ferrocene, nickelocene, cobaltocene, molybdocene dichloride, dicyclopentadienyltitanium dichloride, dichloride. Dicyclopentadienyl zirconium chloride or the like is preferable,
The metal acetylacetone complexes used in the present invention include Li, Na, K, Ag, Au, Tl,
Au, Ga, Co, Cu, Be, Mg, Zn, Cd, H
g, Pb, Mo, Ni, B, Ca, Sr, Ba, Pd,
Pt, In, Se, Ce, Ta, La, Ti, Mn, F
e, Cr, V, Si, Zr and a complex salt of acetylacetone may be mentioned, but manganese (2) acetylacetonate,
Cobalt (2) acetylacetonate and the like are preferable.

【0010】本発明のハロゲン化炭化水素は、炭素数2
〜4の隣接する炭素上に潜在的に脱離しうる少なくとも
1個以上の水素およびハロゲン原子(フッ素、塩素また
は臭素)を含む低級脂肪族ハロゲン化炭化水素である。
具体的には2,2ージクロロー1,1,1−トリフルオ
ロエタン、1,1−ジクロロー1ーフルオロエタン、1
−クロロ−1,1−ジフルオロエタン、1,1,1−ト
リクロロエタン、2−クロロ−1,1,1−トリフルオ
ロエタン、1,2−ジクロロ−1,1−ジフルオロエタ
ン等が挙げられる。
The halogenated hydrocarbon of the present invention has 2 carbon atoms.
~ 4 lower aliphatic halogenated hydrocarbons containing at least one or more hydrogen and halogen atoms (fluorine, chlorine or bromine) potentially removable on adjacent carbons.
Specifically, 2,2-dichloro-1,1,1-trifluoroethane, 1,1-dichloro-1-fluoroethane, 1
-Chloro-1,1-difluoroethane, 1,1,1-trichloroethane, 2-chloro-1,1,1-trifluoroethane, 1,2-dichloro-1,1-difluoroethane and the like can be mentioned.

【0011】本発明の方法で安定化されるアルコール性
水酸基含有化合物としてはメタノール、エタノール、イ
ソプロパノール、nーブタノール、sec−ブタノー
ル、エチレングリコール、プロピレングリコール等のア
ルコール類およびポリウレタン原料のポリオール類があ
る。
Examples of the alcoholic hydroxyl group-containing compound stabilized by the method of the present invention include alcohols such as methanol, ethanol, isopropanol, n-butanol, sec-butanol, ethylene glycol and propylene glycol, and polyols used as a raw material for polyurethane.

【0012】ポリオール類には、アミン系のものとして
N,N,N’,N’−テトラキス(2ーヒドロキシプロ
ピル)エチレンジアミン、N,N,N’−トリス(2ー
ヒドロキシプロピル)ーN’−(2−ヒドロキシエチ
ル)エチレンジアミン、N,N,N’,N’’,N’’
−ペンタキス(2ーヒドロキシプロピル)ジエチレント
リアミンなどが挙げられる他、エチレンオキシドまたは
プロピレンオキシドとエチレンジアミンとの反応による
ポリエーテルポリオール、またアジピン酸、フタル酸な
どとエチレングリコール、プロピレングリコールなどと
の反応によるポリエステルポリオール、さらにはポリ
(オキシプロピレン)シュークロース、ポリ(オキシプ
ロピレン)ソルビトールなどを挙げることができる。
The polyols include N, N, N ', N'-tetrakis (2-hydroxypropyl) ethylenediamine, N, N, N'-tris (2-hydroxypropyl) -N'-as amine type. (2-hydroxyethyl) ethylenediamine, N, N, N ′, N ″, N ″
-Pentakis (2-hydroxypropyl) diethylenetriamine and the like, polyether polyol by reaction of ethylene oxide or propylene oxide with ethylene diamine, polyester polyol by reaction of adipic acid, phthalic acid, etc. with ethylene glycol, propylene glycol, etc. Furthermore, poly (oxypropylene) sucrose, poly (oxypropylene) sorbitol, etc. can be mentioned.

【0013】アミン系のポリオールは非アミン系に比べ
一般に反応性が高いことが知られているが、本発明の安
定剤はアミン系にも有効であり、添加量は発泡剤に対し
0.001〜5重量%、好ましくは0.01〜1重量%
が望ましい。5重量%以上用いることは経済的およびポ
リウレタンの物性面において特に好結果を得ることはな
く、必要ではない。
It is known that amine-based polyols are generally higher in reactivity than non-amine-based polyols, but the stabilizer of the present invention is effective for amine-based polyols, and the addition amount is 0.001 with respect to the foaming agent. ~ 5% by weight, preferably 0.01 to 1% by weight
Is desirable. It is not necessary to use 5% by weight or more because economically and in terms of physical properties of polyurethane, particularly good results cannot be obtained.

【0014】安定剤の添加方法は、予め発泡剤またはア
ルコール性水酸基含有化合物に添加することができ、ま
たプレミックスの中に添加しておくこともできる。発泡
剤に不溶の安定剤は微量のメタノール、アセトン等に溶
解することにより添加することができる。
The stabilizer may be added in advance to the foaming agent or the alcoholic hydroxyl group-containing compound, or may be added to the premix. The stabilizer insoluble in the foaming agent can be added by dissolving it in a very small amount of methanol, acetone or the like.

【0015】ハロゲン化炭化水素は、溶剤において溶解
性を向上させるために、また噴射剤において薬剤、香料
等の溶解性を高める目的でアルコール性水酸基を含有す
る化合物と混合されることが多く、本発明の安定化方法
は好適に使用できる。しかしながら、本発明の効果はウ
レタンフォーム製造において最も有効であり、本安定剤
の添加により、プレミックスは長期間安定に貯蔵するこ
とができ、またポリウレタンフォームは物性を損うこと
なく発泡形成することができる。
Halogenated hydrocarbons are often mixed with a compound containing an alcoholic hydroxyl group for the purpose of improving the solubility in a solvent and for improving the solubility of a drug, a fragrance, etc. in a propellant. The stabilization method of the invention can be preferably used. However, the effect of the present invention is most effective in the production of urethane foam, and by adding the stabilizer, the premix can be stably stored for a long period of time, and the polyurethane foam can be foamed without impairing the physical properties. You can

【0016】以下、本発明を実施例により詳細に説明す
るが、本発明はこれらの実施例に限定されるものではな
い。
Hereinafter, the present invention will be described in detail with reference to examples, but the present invention is not limited to these examples.

【0017】[0017]

【実施例】実施例1〜5 N,N,N’,N’−テトラキス(2ーヒドロキシプロ
ピル)エチレンジアミン20重量部、ジメチルシクロヘ
キシルアミン0.4重量部、水0.3重量部、整泡剤
(東レダウコーニングシリコン社製SHー193)0.
3重量部、発泡剤(1,1−ジクロロー1ーフルオロエ
タン)8重量部を混合したプレミックスに、安定剤を発
泡剤に対し0.1重量部添加し、100ml耐圧ガラス
管に密封し、90℃、3日間放置した。1,1−ジクロ
ロー1ーフルオロエタンに不溶の安定剤は予め5重量%
メタノール溶液とし、プレミックスに添加した。期間終
了後、60℃における耐圧ガラス管中の気相部および液
相部の有機物組成をガスクロマトグラフィーにより分析
した。但し液相部の有機物は浴温60℃において蒸留し
た留分を分析した。試験終了後のプレミックスのpHは
イソプロパノール/水混合溶液(10/6容積比) にプ
レミックスに対し1/6量(重量比)を加え混合攪拌し
測定した。また色度はJISK−6901に準じ、ガー
ドナー色度にて表示した。結果を表1および表2に示
す。主な分解生成物は1ークロロー1ーフルオロエタン
(HCFC−151a)、1−クロロー1ーフルオロエ
チレン(HCFC−1131a)および1,1−ジクロ
ロエチレン(HCFC−1130a)であるが、1,1
−ジクロロエチレンの生成はほとんど認められなかっ
た。
Examples 1 to 5 N, N, N ', N'-tetrakis (2-hydroxypropyl) ethylenediamine 20 parts by weight, dimethylcyclohexylamine 0.4 parts by weight, water 0.3 parts by weight, foam stabilizer (Toray Dow Corning Silicon Co. SH-193)
To a premix prepared by mixing 3 parts by weight and 8 parts by weight of a foaming agent (1,1-dichloro-1-fluoroethane), 0.1 part by weight of a stabilizer was added to the foaming agent, and the mixture was sealed in a 100 ml pressure-resistant glass tube and heated at 90 ° C. It was left for 3 days. The stabilizer insoluble in 1,1-dichloro-1-fluoroethane is 5% by weight in advance.
It was made into a methanol solution and added to the premix. After the end of the period, the organic composition of the gas phase part and the liquid phase part in the pressure resistant glass tube at 60 ° C. was analyzed by gas chromatography. However, for the organic matter in the liquid phase part, a fraction distilled at a bath temperature of 60 ° C. was analyzed. The pH of the premix after the test was measured by adding 1/6 amount (weight ratio) of the premix to the isopropanol / water mixed solution (10/6 volume ratio), mixing and stirring. The chromaticity is displayed in Gardner chromaticity according to JISK-6901. The results are shown in Tables 1 and 2. The main decomposition products are 1-chloro-1-fluoroethane (HCFC-151a), 1-chloro-1-fluoroethylene (HCFC-1131a) and 1,1-dichloroethylene (HCFC-1130a),
Almost no formation of dichloroethylene was observed.

【0018】[0018]

【表1】 [Table 1]

【0019】[0019]

【表2】 比較例1、2 実施例1〜5のプレミックスに安定剤を添加しない(比
較例1)、または安定剤としてαーメチルスチレン0.
1重量部(発泡剤に対し)添加(比較例2)し、実施例
1〜5と同様にして行なった結果を表1および表2に示
す。
[Table 2] Comparative Examples 1 and 2 No stabilizer was added to the premixes of Examples 1 to 5 (Comparative Example 1), or α-methylstyrene of 0.1.
Table 1 and Table 2 show the results obtained by adding 1 part by weight (based on the foaming agent) (Comparative Example 2) and performing the same procedure as in Examples 1 to 5.

【0020】[0020]

【発明の効果】本発明の方法によれば、表1および表2
より明らかな様に、ハロゲン化炭化水素とアルコール性
水酸基含有化合物が接触する条件においてもハロゲン化
水素の脱離したオレフィンの生成は顕著に抑制され、特
に硬質ウレタンフォーム製造におけるハロゲン化炭化水
素よりなる発泡剤を安定化することができる。
According to the method of the present invention, Table 1 and Table 2
As is clearer, even under the condition that a halogenated hydrocarbon and an alcoholic hydroxyl group-containing compound come into contact with each other, the production of an olefin from which a hydrogen halide is eliminated is remarkably suppressed. The foaming agent can be stabilized.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 ハロゲン化炭化水素にメタロセン類また
は金属アセチルアセトン錯体から選ばれる1種以上を添
加することを特徴とするハロゲン化炭化水素の安定化方
法。
1. A method for stabilizing a halogenated hydrocarbon, which comprises adding at least one selected from metallocenes and metal acetylacetone complexes to the halogenated hydrocarbon.
【請求項2】 ハロゲン化炭化水素が炭素数2ないし4
で、かつ隣接する炭素上に潜在的に脱離しうる少なくと
も1個以上の水素およびハロゲン原子をそれぞれ有する
化合物である請求項1記載の安定化方法。
2. The halogenated hydrocarbon has 2 to 4 carbon atoms.
The stabilization method according to claim 1, which is a compound having at least one or more hydrogen and halogen atoms which can potentially be eliminated on adjacent carbon atoms.
【請求項3】 ウレタンフォーム製造において、請求項
1記載の安定化方法を適用することを特徴とするプレミ
ックスの貯蔵安定化方法。
3. A method for stabilizing storage of a premix, which comprises applying the stabilization method according to claim 1 in the production of urethane foam.
JP3320797A 1991-12-04 1991-12-04 Method for stabilizing halogenated hydrocarbon Pending JPH05156062A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3320797A JPH05156062A (en) 1991-12-04 1991-12-04 Method for stabilizing halogenated hydrocarbon

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3320797A JPH05156062A (en) 1991-12-04 1991-12-04 Method for stabilizing halogenated hydrocarbon

Publications (1)

Publication Number Publication Date
JPH05156062A true JPH05156062A (en) 1993-06-22

Family

ID=18125355

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3320797A Pending JPH05156062A (en) 1991-12-04 1991-12-04 Method for stabilizing halogenated hydrocarbon

Country Status (1)

Country Link
JP (1) JPH05156062A (en)

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