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JP2855688B2 - Method of preserving double metal cyanide complex catalyst - Google Patents
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JP2855688B2 - Method of preserving double metal cyanide complex catalyst - Google Patents

Method of preserving double metal cyanide complex catalyst

Info

Publication number
JP2855688B2
JP2855688B2 JP1224642A JP22464289A JP2855688B2 JP 2855688 B2 JP2855688 B2 JP 2855688B2 JP 1224642 A JP1224642 A JP 1224642A JP 22464289 A JP22464289 A JP 22464289A JP 2855688 B2 JP2855688 B2 JP 2855688B2
Authority
JP
Japan
Prior art keywords
complex catalyst
cyanide complex
metal cyanide
double metal
organic ligand
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.)
Expired - Fee Related
Application number
JP1224642A
Other languages
Japanese (ja)
Other versions
JPH0389944A (en
Inventor
和彦 山田
富雄 鑓田
弘光 武安
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.)
AGC Inc
Original Assignee
Asahi 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 Asahi Glass Co Ltd filed Critical Asahi Glass Co Ltd
Priority to JP1224642A priority Critical patent/JP2855688B2/en
Publication of JPH0389944A publication Critical patent/JPH0389944A/en
Application granted granted Critical
Publication of JP2855688B2 publication Critical patent/JP2855688B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/52Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Landscapes

  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Polyethers (AREA)

Description

【発明の詳細な説明】 [産業上野利用分野] 本発明は複合金属シアン化物錯体触媒の保存方法に関
するものである。
The present invention relates to a method for preserving a double metal cyanide complex catalyst.

[従来の技術] 従来、アルキレンオキサイドなどのモノエポキシドを
開環反応させる触媒として複合金属シアン化物錯体が知
られている(US 3278457,US 3278458,US 3278459)。こ
のとき用いられる複合金属シアン化物錯体触媒の製造方
法はUS 3427256,US 3941849,US 4472560,US 4477589明
細書などにより提案されている。
[Prior Art] Conventionally, double metal cyanide complexes have been known as catalysts for ring-opening reactions of monoepoxides such as alkylene oxides (US 3278457, US 3278458, US 3278459). The production method of the double metal cyanide complex catalyst used at this time is proposed in US Pat. No. 3,427,256, US Pat. No. 3,418,491, US Pat. No. 4,472,560, US Pat.

[発明の解決しようとする問題点] 上記複合金属シアン化物錯体触媒においては、長期間
にわたる保存安定性が悪く、触媒の反応誘導期間が伸
び、反応速度も低下するという欠点を有している。
[Problems to be Solved by the Invention] The above-mentioned double metal cyanide complex catalyst has a drawback that storage stability over a long period of time is poor, the reaction induction period of the catalyst is extended, and the reaction rate is reduced.

[問題点を解決するための手段] 本発明は前述の問題点を解決すべくなされたものであ
りハロゲン化金属塩水溶液とアルカリ金属シアノメタレ
ート水溶液と有機配位子による複合金属シアン化物錯体
触媒の保存方法において、合成した複合金属シアン化物
錯体触媒を、合成に用いた有機配位子、またはそれ以外
の有機配位子中において重量比0.01〜1000で、好ましく
は重量比0.1以上で保存する保存方法と、この複合金属
シアン化物錯体触媒を用いて開環反応させるモノエポキ
シド中で重量比0.01〜1000で、好ましくは0.1以上で保
存する保存方法とを提供するものである。有機配位子と
してエーテル、エステル、アルコール、アルデヒド、ケ
トン、アミド、ニトリル、スルフィドの中より選ぶ1種
類、或は2種類以上を用いる。
Means for Solving the Problems The present invention has been made to solve the above problems, and is a composite metal cyanide complex catalyst comprising an aqueous solution of a metal halide, an aqueous solution of an alkali metal cyanometalate, and an organic ligand. In the storage method, the synthesized double metal cyanide complex catalyst is stored at a weight ratio of 0.01 to 1000 in the organic ligand used for the synthesis or other organic ligands, preferably at a weight ratio of 0.1 or more. It is intended to provide a storage method and a storage method in which a monoepoxide subjected to a ring opening reaction using the double metal cyanide complex catalyst is stored at a weight ratio of 0.01 to 1000, preferably 0.1 or more. As the organic ligand, one or more selected from ether, ester, alcohol, aldehyde, ketone, amide, nitrile, and sulfide is used.

本発明において複合金属シアン化物錯体触媒のモノエ
ポキシドを開環重合させる機構は必ずしも明確になって
いないが、複合金属シアン化物の有機配位子の配位状態
が触媒活性に大きな影響を与えているものと考えられ
る。そのため、有機配位子中で接触させながらの保存が
反応誘導時間及び反応速度に対し良い結果を導くに至っ
たものと考えられる。更に本発明においてはその反応時
間が複合金属シアン化物錯体触媒合成直後の値よりも短
くなっており、また反応速度も向上していることが認め
られた。
In the present invention, the mechanism of ring-opening polymerization of the monoepoxide of the double metal cyanide complex catalyst is not always clear, but the coordination state of the organic ligand of the double metal cyanide has a great influence on the catalytic activity. It is considered something. Therefore, it is considered that the preservation while being brought into contact with the organic ligand led to a good result with respect to the reaction induction time and the reaction rate. Furthermore, in the present invention, it was confirmed that the reaction time was shorter than the value immediately after the synthesis of the double metal cyanide complex catalyst, and that the reaction rate was also improved.

[実施例] 実施例1 有機配位子としてジエチレングリコールジメチルエー
テルを用いた複合金属シアン化物錯体触媒1gに対し、ジ
エチレングリコールジメチルエーテル1gを加え、一定期
間保存した。
[Example] Example 1 1 g of diethylene glycol dimethyl ether was added to 1 g of a double metal cyanide complex catalyst using diethylene glycol dimethyl ether as an organic ligand, and stored for a certain period.

実施例2 有機配位子としてジエチレングリコールジメチルエー
テルを用いた複合金属シアン化物錯体触媒1gに対し、プ
ロピレンオキサイド1gを加え、一定期間保存した。
Example 2 1 g of propylene oxide was added to 1 g of a double metal cyanide complex catalyst using diethylene glycol dimethyl ether as an organic ligand, and the mixture was stored for a certain period.

実施例3 有機配位子としてジエチレングリコールジメチルエー
テルを用いた複合金属シアン化物錯体触媒1gに対し、エ
チレングリコールジメチルエーテル1gを加え、一定期間
保存した。
Example 3 1 g of ethylene glycol dimethyl ether was added to 1 g of a double metal cyanide complex catalyst using diethylene glycol dimethyl ether as an organic ligand, and stored for a certain period.

比較例1 有機配位子としてジエチレングリコールジメチルエー
テルを用いた複合金属シアン化物錯体触媒を一定期間保
存した。
Comparative Example 1 A double metal cyanide complex catalyst using diethylene glycol dimethyl ether as an organic ligand was stored for a certain period of time.

上記触媒を18日間保存の後、分子量1000のトリオール
に対して、この触媒を用いてプロピレンオキサイドの開
環重合の反応を行いその誘導時間及び反応速度を測定し
保存前の値との比をとり下表に示した。
After storage of the above catalyst for 18 days, a ring-opening polymerization reaction of propylene oxide was performed on triol having a molecular weight of 1,000 using this catalyst, the induction time and reaction rate were measured, and the ratio to the value before storage was determined. It is shown in the table below.

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】ハロゲン化金属塩水溶液とアルカリ金属シ
アノメタレート水溶液と有機配位子による複合金属シア
ン化物錯体触媒の保存方法において、合成した複合金属
シアン化物錯体触媒を、合成に用いた有機配位子、また
はそれ以外の有機配位子中で保存する保存方法。
1. A method for preserving a double metal cyanide complex catalyst comprising a metal halide aqueous solution, an alkali metal cyanometalate aqueous solution and an organic ligand, wherein the synthesized double metal cyanide complex catalyst is prepared by using an organic metal salt used for the synthesis. Preservation method to store in ligand or other organic ligand.
【請求項2】ハロゲン化金属塩水溶液とアルカリ金属シ
アノメタレート水溶液と有機配位子による複合金属シア
ン化物錯体触媒の保存方法において、この複合金属シア
ン化物錯体触媒を用いて開環反応させるモノエポキシド
中で保存する保存方法。
2. A method for preserving a double metal cyanide complex catalyst using a metal halide aqueous solution, an alkali metal cyanometalate aqueous solution and an organic ligand, wherein a monoepoxide is subjected to a ring opening reaction using the double metal cyanide complex catalyst. How to save in.
【請求項3】有機配位子としてエーテル、エステル、ア
ルコール、アルデヒド、ケトン、アミド、ニトリル、ス
ルフィドの中より選ぶ1種類、或は2種類以上を用いる
特許請求の範囲第1項または第2項記載の保存方法。
3. The method according to claim 1, wherein one or more selected from ethers, esters, alcohols, aldehydes, ketones, amides, nitriles and sulfides are used as the organic ligand. How to save the description.
JP1224642A 1989-09-01 1989-09-01 Method of preserving double metal cyanide complex catalyst Expired - Fee Related JP2855688B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1224642A JP2855688B2 (en) 1989-09-01 1989-09-01 Method of preserving double metal cyanide complex catalyst

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1224642A JP2855688B2 (en) 1989-09-01 1989-09-01 Method of preserving double metal cyanide complex catalyst

Publications (2)

Publication Number Publication Date
JPH0389944A JPH0389944A (en) 1991-04-15
JP2855688B2 true JP2855688B2 (en) 1999-02-10

Family

ID=16816918

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1224642A Expired - Fee Related JP2855688B2 (en) 1989-09-01 1989-09-01 Method of preserving double metal cyanide complex catalyst

Country Status (1)

Country Link
JP (1) JP2855688B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2619138B2 (en) * 1990-11-27 1997-06-11 旭硝子株式会社 Preservation method of double metal cyanide complex

Also Published As

Publication number Publication date
JPH0389944A (en) 1991-04-15

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