KR19980075997A - Organic Ti-P catalyst, preparation method thereof and preparation method of polyester imide using same - Google Patents

Organic Ti-P catalyst, preparation method thereof and preparation method of polyester imide using same Download PDF

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KR19980075997A
KR19980075997A KR1019970012437A KR19970012437A KR19980075997A KR 19980075997 A KR19980075997 A KR 19980075997A KR 1019970012437 A KR1019970012437 A KR 1019970012437A KR 19970012437 A KR19970012437 A KR 19970012437A KR 19980075997 A KR19980075997 A KR 19980075997A
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catalyst
organic
polyesterimide
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preparation
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허완수
박이순
이태형
박민규
권찬동
이상원
조익수
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허완수
박이순
김장연
삼화페인트공업 주식회사
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/16Polyester-imides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1003Preparatory processes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1003Preparatory processes
    • C08G73/1007Preparatory processes from tetracarboxylic acids or derivatives and diamines
    • C08G73/1021Preparatory processes from tetracarboxylic acids or derivatives and diamines characterised by the catalyst used

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
  • Paints Or Removers (AREA)

Abstract

본 발명은 폴리에스테르이미드 합성용 촉매, TinP O11C14H45(여기서, n은 1 내지 3의 정수), 그의 제조방법 및 이를 이용한 폴리에스테르이미드의 제조방법에 관한 것이다.The present invention relates to a catalyst for synthesizing polyester imide, Ti n PO 11 C 14 H 45 (where n is an integer of 1 to 3), a method for preparing the same, and a method for preparing polyester imide using the same.

본 발명의 촉매 및 그의 제조방법은 신규한 것이며, 본 발명에 따른 촉매를 이용하여 제조된 폴리에스테르이미드는 고내열성 전기절연 도료 중 마그네트 와이어 코팅(magnet wire coating)의 기본 수지로서 투명도와 색상이 우수할 뿐만 아니라 내열성, 유연성 및 내마모성이 우수하다.The catalyst of the present invention and its manufacturing method are novel, and the polyester imide prepared using the catalyst according to the present invention is excellent in transparency and color as a basic resin of magnet wire coating in high heat-resistant electrical insulating paint. In addition to excellent heat resistance, flexibility and wear resistance.

Description

유기 Ti-P 계 촉매, 그의 제조방법 및 이를 이용한 폴리에스테르이미드의 제조방법Organic Ti-P catalyst, preparation method thereof and preparation method of polyester imide using same

본 발명은 유기 Ti-P 계 촉매, 그의 제조방법 및 이를 이용한 폴리에스테르이미드의 제조방법에 관한 것이다.The present invention relates to an organic Ti-P catalyst, a method for producing the same, and a method for producing a polyesterimide using the same.

본 발명에 따른 유기 Ti-P계 촉매는 반응온도를 낮추고 반응시간을 단축시킬뿐 아니라 분해, 색상 발현 등을 일으키는 부반응을 최소화함으로써 고내열 전기절연 도료, 특히 고전압용 마그네트 와이어 코팅(magnet wire coating)의 기본 수지로서 사용되는 내열성, 유연성 및 내마모성이 우수할 뿐만 아니라 투명도와 색상이 우수한 폴리에스테르이미드 수지를 제조하는데 유용하다.The organic Ti-P catalyst according to the present invention not only lowers the reaction temperature and shortens the reaction time, but also minimizes side reactions that cause decomposition, color development, and the like. It is useful for preparing polyesterimide resins having excellent heat resistance, flexibility and wear resistance as well as excellent transparency and color used as basic resins.

고내열성 마그네트 와이어 코팅용 기본 수지로는 폴리에스테르계, 폴리 이미드계 혹은 폴리에스테르이미드계 수지가 사용되어 왔다. 미극특허 제 3,342,780호에서는 마그네트 와이어 코팅용 기본 수지로서 폴리에스테르계 수지를 합성하였고 디메틸테레프탈레이트와 에틸렌글리콜을 축중합함에 있어서 에틸렌글리콜의 일부를 3관능성 환식 화합물인 트리스(2-히드록시에틸) 이소시아누레이트로 치환함으로써 내열성을 향상시킬 수 있다고 기재하고 있다. 또, 미국 특허 제 3,426,098호에서는 마그네트 와이어, 코팅용 기본 수지로서 트리멜리트산 무수물, 메틸렌 디아닐린, 에틸렌글리콜 및 트리스(2-히드록시에틸) 이소시아누레이트를 N-메틸 피롤리디논 용매에 용해시키고 축중합하여 중합체 사슬 내에 이미드 구조를 도입한 폴리에스테르이미드를 합성함으로서 내열성이 향상된다고 하였다. 미국 특허 제 3,697,471호에서도 트리멜리트산 무수물, 메틸렌 디아닐린, 에틸렌 글리콜 및 트리스(2-히드록시에틸) 이소시아누레이트를 원료로 하여 축중합 반응을 통하여 폴리에스테르이미드 수지를 합성하였으며 N-메틸피롤리디논 용매 대신에 m-크레졸을 용매로 사용함으로서 폴리에스테르 이미드를 일회 반응으로 얻을 수 있다고 기재하고 있다.Polyester, polyimide or polyesterimide resins have been used as basic resins for high heat resistance magnet wire coating. In US Patent No. 3,342,780, a polyester resin was synthesized as a base resin for magnet wire coating, and in the polycondensation of dimethyl terephthalate and ethylene glycol, tris (2-hydroxyethyl), a trifunctional cyclic compound, was partially used. It is described that heat resistance can be improved by substituting with isocyanurate. U.S. Patent No. 3,426,098 also discloses dissolving trimellitic anhydride, methylene dianiline, ethylene glycol and tris (2-hydroxyethyl) isocyanurate in N-methyl pyrrolidinone solvent as a base wire for magnet wires and coatings. It was said that the heat resistance was improved by synthesizing the polyester imide which introduced the imide structure in the polymer chain by polycondensation. US Pat. No. 3,697,471 also synthesized a polyesterimide resin through condensation polymerization using trimellitic anhydride, methylene dianiline, ethylene glycol and tris (2-hydroxyethyl) isocyanurate as raw materials. It is described that polyester imide can be obtained in one reaction by using m-cresol as a solvent instead of a lolidinone solvent.

이와 같은 종래의 고내열성 마그네트 와이어 코팅용 기본 수지 합성법들은 중합반응을 촉진 시키는 촉매에 대해서 고려하지 않아 중합 온도가 220~230℃ 정도로 높고 반응시간도 14시간 이상으로 장시간을 필요로 한다. 축중합 반응은 가역반응이므로 반응온도가 높고 반응시간이 길면 정반응이 아닌 역반응 및 분해, 색상 발현 등 부반응이 증가되어 합성되는 폴리에스테르 혹은 폴리에스테르이미드 수지의 변색, 부반응물의 축적 등 문제가 일어나게 된다.Such conventional resins for high heat resistance magnet wire coating base resin synthesis method does not consider the catalyst for promoting the polymerization reaction, the polymerization temperature is as high as 220 ~ 230 ℃ and the reaction time requires a long time as 14 hours or more. Since the polycondensation reaction is a reversible reaction, if the reaction temperature is high and the reaction time is long, problems such as discoloration of the polyester or polyesterimide resin synthesized due to increased side reactions such as reverse reaction, decomposition, and color development rather than forward reaction may occur. .

폴리에스테르의 합성에 있어서 티타늄 알콕사이드는 촉매 작용을 한다고 알려져 있다(미국 특허 4,007,218). 그리고 티타늄 알콕사이드는 축중합 반응의 정반응 뿐만 아니라 역반응 및 분해 반응을 동시에 촉진 시키므로 생성되는 폴리에스테르의 색상을 갈색으로 변화시키는 단점이 있다.Titanium alkoxides are known to catalyze the synthesis of polyesters (US Pat. No. 4,007,218). And titanium alkoxide has the disadvantage of changing the color of the resulting polyester brown because it promotes the forward reaction and decomposition reaction as well as the forward reaction of the polycondensation reaction.

이렇게 제조된 수지에 코팅에 필요한 첨가제 들을 넣고 마그네트 와이어 코팅을 하면 부반응물의 축적으로인한 핀 홀(pin hole)의 발생, 코팅된 마그네트와이어의 색상 조절의 난이, 내열성의 저하, 유연성의 저하 등 문제를 초래하게 된다.When the magnet wire is coated with the additives necessary for the coating in the resin thus prepared, pin holes are generated due to the accumulation of side reactants, difficulty of color control of the coated magnet wire, deterioration of heat resistance and deterioration of flexibility, etc. It causes problems.

본 발명자들은 위와 같은 문제점을 해결하고자 연구를 거듭한 결과, 특정 유기 Ti-P계 촉매를 사용함으로써 반응온도를 낮추고 반응시간을 단축함으로써 내열성, 유연성 및 내마모성이 우수한 폴리에스테르이미드를 제조할 수 있다는 사실을 발견하고, 본 발명을 완성하기에 이르렀다.The present inventors have conducted a study to solve the above problems, the fact that by using a specific organic Ti-P-based catalyst can lower the reaction temperature and shorten the reaction time to produce a polyesterimide excellent in heat resistance, flexibility and wear resistance It has been found that the present invention has been completed.

종래, 고내열성의 마그네트와 와이어 코팅용 기본 수지로서 폴리에스테르 혹은 폴리에스테르이미드를 합성하는 방법들은 축중합 반응 촉매에 대한 고려를 하드 기본 수지 합성에 있어서 보다 낮은 온도에서 반응을 진행시키고 반응시간을 단축하는 것이 중요하다.Conventionally, methods for synthesizing polyester or polyesterimide as a base material for high heat-resistant magnets and wire coatings advance the reaction at a lower temperature and shorten the reaction time in the synthesis of a hard base resin considering the polymerization catalyst. It is important to do.

따라서, 본 발명의 목적은 폴리에스테르 혹은 폴리에스테르이미드 기본수지 합성에 있어서 보다 낮은 온도에서 반응을 진행시키고 반응시간을 단축시키기 위한 유기 Ti-P계 촉매를 제공하는 데 있다.Accordingly, an object of the present invention is to provide an organic Ti-P catalyst for progressing the reaction at a lower temperature and shortening the reaction time in the synthesis of polyester or polyesterimide base resin.

본 발명에 따른 유기 Ti-P계 촉매는 TinP O11C14H45(여기서, n은 1 내지 3의 정수)으로 나타내진다.The organic Ti-P based catalyst according to the present invention is represented by Ti n PO 11 C 14 H 45 , where n is an integer of 1 to 3.

본 발명의 또 다른 목적은 티타늄 클로라이드(titinium(IV) chloride)를 유기 포스페이트 인산 또는 인산에스테르를 CCI4또는 n-헥센의 촉매 중에서 20~30℃에서 30분간 교반한 후, 다시 30분 동안 에탄올과 반응시킨 다음 에틸렌글리콜을 가함으로써 일반식 TinP O11C14H45(여기서, n은 1 내지 3의 정수)으로 나타내지는 유기 Ti-P계 촉매를 제조하는 방법을 제공한다는데 있다. 유기포스페이트의 바람직한 예로는 트리메틸, 트리에틸 또는 트리페닐 포스페이트가 있다.Still another object of the present invention is to agitate titanium chloride (titinium (IV) chloride) with organic phosphate phosphoric acid or phosphate ester in a catalyst of CCI 4 or n-hexene at 20-30 ° C. for 30 minutes, and then again with ethanol for 30 minutes. It is to provide a method for producing an organic Ti-P-based catalyst represented by the general formula Ti n PO 11 C 14 H 45 (where n is an integer of 1 to 3) by the addition of ethylene glycol. Preferred examples of organophosphates are trimethyl, triethyl or triphenyl phosphate.

본 발명의 또 다른 목적은 트리멜리트산 무수물과 메틸렌 디아닐린을 m-크레졸 용매중에서 반응시켜 디애시디이미드(diacid diimide)를 합성한 다음 에틸렌글리콜 및 트리스(2-히드록시에틸)이소시아누레이트와 함께 일반식 TinP O11C14H45(여기서, n은 1 내지 3의 정수)으로 나타내지는 유기 Ti-P계 촉매를 첨가하여 축중합시킴으로써 폴리에스테르이미드를 제조하는 방법을 제공하는데 있다.It is still another object of the present invention to synthesize diacid diimide by reacting trimellitic anhydride and methylene dianiline in a m-cresol solvent, followed by ethylene glycol and tris (2-hydroxyethyl) isocyanurate. To provide a method for producing a polyesterimide by addition and polycondensation of an organic Ti-P-based catalyst represented by the general formula Ti n PO 11 C 14 H 45 (where n is an integer of 1 to 3).

본 발명의 유기 Ti-P계 촉매는 티타늄 클로라이드를 트리에틸 포스페이트 및 에탄올과 반응시켜 열안정제의 기능이 있는 포스페이트 기를 리간드로 도입함으로서 내열성이 우수한 촉매가 된다는 점에서 다른 티타늄 계 촉매와 구분이 된다. 실제 트리에틸 포스페이트는 폴리에스테르 혹은 폴리에스테르이미드의 합성에 열안정제로 사용 되며 이를 첨가하여 합성한 폴리에스테르 혹은 폴리에스테르이미드는 분해 또는 역반응이 억제되어 백색도가 우수하다고 알려져 있다. 본 발명에 있어서는 이러한 열안정제의 기능이 있는 트리에틸 포스페이트를 에탄올과 함께 티타늄 클로라이드와 반응시켜 새로운 유기 Ti-P 계 화합물을 만듦으로서 촉매 작용과 열안정제의 작용을 동시에 할 수 있는 촉매를 합성한 것이 특징이다.The organic Ti-P catalyst of the present invention is distinguished from other titanium catalysts in that titanium chloride is reacted with triethyl phosphate and ethanol to introduce a phosphate group having a function of a thermal stabilizer as a ligand, thereby making the catalyst excellent in heat resistance. In fact, triethyl phosphate is used as a thermal stabilizer in the synthesis of polyester or polyesterimide, and polyester or polyesterimide synthesized by adding it is known to have excellent whiteness due to inhibition of decomposition or reverse reaction. In the present invention, a triethyl phosphate having a function of the thermal stabilizer is reacted with titanium chloride together with ethanol to form a new organic Ti-P compound, thereby synthesizing a catalyst capable of simultaneously acting as a catalyst and a thermal stabilizer. It is characteristic.

이하, 실시에에서는 본 발명을 더욱 자세히 설명하지만, 본 발명의 범위가 실시예 만으로 한정되는 것은 아니다.Hereinafter, although an Example demonstrates this invention still in detail, the scope of the present invention is not limited only to an Example.

[실시예 1]Example 1

(유기 Ti-P계 촉매의 합성)Synthesis of Organic Ti-P Catalyst

상온에서 질소로 치환된 티타늄 클로라이드 0.05 mole을 공기와 접촉하지 않는 조건하에서 100ml 질소로 치환된 3구 플라스크에 넣고 0.017 mole의 트리에틸 포스페이트를 30분에 걸쳐 서서히 교반하면서 적가하고 이때 발생하는 가스를 제거 하였다. 반응이 끝나고 반응열이 상온으로 될 때까지 냉각한 후 0.15 mole의 에탄올을 다시 30분에 걸쳐 교반하면서 적가 하여 반응시킨 후, 24g의 에틸렌 글리콜을 가하여 티타늄 대 인의 원소가 3:1인 유기 Ti-P계 촉매를 제조 하였다.0.05 mole of titanium chloride substituted with nitrogen at room temperature was added to a 100 ml nitrogen-substituted three-necked flask under no contact with air, and 0.017 mole of triethyl phosphate was slowly added dropwise over 30 minutes to remove the gas. It was. After the reaction was completed and the reaction heat was cooled to room temperature, 0.15 mole of ethanol was added dropwise with stirring over 30 minutes, followed by the addition of 24 g of ethylene glycol. The catalyst was prepared.

[실시예 2]Example 2

(폴리에스테르이미드 수지의 합성 1)(Synthesis 1 of polyester imide resin)

상온에서 기계식 교반기, 분리 칼럼, 응축기 및 온도 조절기가 장치된 1L의 수지 합성용 반응기에 트리멜리트산 무수물 115.7g, 메틸렌 디아닐린 59.7g, 에틸렌글리콜 36.9g, 트리스(2-히드록시에틸)이소시아누레이트 70.5g, m-크레졸 424.2g을 투입하였다. 다음 앞에서 합성한 유기 Ti-P계 촉매를 반응물 고형분 대비 0, 200, 400 및 800 ppm이 되도록 각각 투입하고 반응기 안을 질소로 치환하였다. 반응기를 둘러싼 히팅 멘틀에 열을 가하며 반응물이 녹게 되면 교반을 시작하고 반응물의 온도를 150℃까지 30분에 걸쳐 올렸다. 이후 교반기의 속도를 250 rpm으로 고정하고 반응물의 온도를 30분마다 10℃씩 올려 210℃까지 승온 시키며 부반응물인 물을 제거하였다. 부반응물인 물은 반응물의 온도가 160℃일 때부터 응축기를 통해 유출 되기 시작했으며 짙은 황토색이던 반응물은 연한 노란색의 슬러리 상태를 거쳐 210℃에서는 점성이 있는 투명한 용액으로 변하였다. 반응물이 210℃에서 투명한 담황색의 점성이 있는 액체상으로 얻어지기 까지의 중합 반응 시간을 보면 표 1에 보듯이 유기 Ti-P계 촉매를 첨가 하지 않을 경우 3시간 50분이 걸리나 촉매의 투입량이 증가할 수록 반응시간이 현저히 단축 됨을 볼 수 있다. 또 표 1에서 유기 Ti-P계 촉매를 사용하여 제조된 폴리에스테르이미드 기본 수지는 투명한 담황색으로 얻어 졌으나 촉매를 첨가하지 않은 경우는 불투명한 짙은 갈색으로 얻어졌다.115.7 g of trimellitic anhydride, 59.7 g of methylene dianiline, 36.9 g of ethylene glycol, and tris (2-hydroxyethyl) isocyanate in a 1L resin synthesis reactor equipped with a mechanical stirrer, a separation column, a condenser and a temperature controller at room temperature 70.5 g of anurate and 424.2 g of m-cresol were added thereto. Next, the organic Ti-P catalyst synthesized above was added to 0, 200, 400, and 800 ppm relative to the solids of the reactants, and the reactor was replaced with nitrogen. Heat was applied to the heating mantle surrounding the reactor and when the reactant melted, stirring was started and the temperature of the reactant was raised to 150 ° C. over 30 minutes. Thereafter, the speed of the stirrer was fixed at 250 rpm, and the temperature of the reactant was raised to 10 ° C. by 30 ° C. every 30 minutes to remove water as a side reaction. Water, which is a side reactant, began to flow through the condenser when the temperature of the reactant was 160 ° C. The reactant, which was dark yellow, changed to a viscous transparent solution at 210 ° C through a pale yellow slurry. The polymerization time from the reaction to the clear, pale yellow viscous liquid phase at 210 ° C. shows 3 hours and 50 minutes without the addition of the organic Ti-P catalyst, as shown in Table 1. It can be seen that the reaction time is significantly shortened. Also, in Table 1, the polyesterimide base resin prepared using the organic Ti-P catalyst was obtained in a clear pale yellow color, but when the catalyst was not added, an opaque dark brown color was obtained.

[표 1]TABLE 1

유기 Ti-P계 촉매량에 따른 중합 반응 시간 및 폴리에스테르이미드의 물성Polymerization Reaction Time and Physical Properties of Polyesterimide According to Organic Ti-P Catalysts

주) *PE1=폴리에스테르이미드Note) * PE1 = polyester imide

[실시예 3]Example 3

(폴리에스테르이미드 수지의 합성 2)(Synthesis 2 of polyester imide resin)

상온에서 1L의 반응기에 트리멜리트산 무수물 115.7g, 메틸렌 디아닐린 59.7g, m-크레졸 424.2g을 투입하고 반응기 안을 질소로 치환하였다. 반응기를 가열하여 반응물이 녹으면 교반을 시작하고 30분에 걸쳐 반응물의 온도를 150℃로 상온시키고 150℃에서 1시간 동안 교반하였다. 이후 부반응물인 물을 제거하면서 반응물의 온도를 30분에 걸쳐 10℃씩 올려 180℃에서 폴리에스테르이미드수지의 중간체인 디애시드 디이미드를 노란색의 슬러리 상태로 얻었다. 에틸렌 글리콜 36.9g, 트리스(2-히드록시에틸) 이소시아누레이트 70.5g 그리고 유기 Ti-P계 촉매를 반응물 고형분 대비 0, 200, 400 및 600 ppm으로 변화 시키면서 투입하고 반응물을 190℃로 승온 시킨 후 30분마다 10℃씩 210℃까지 승온시켰다. 210℃에서 계속 반응을 시키면서 반응물이 투명한 담황색의 용액으로 변화하는 시간을 측정한 결과를 표 2에 나타내었다. 표 2에서 유기 Ti-P계 촉매를 도입함으로서 마그네트 와이어 코팅에 쓰이는 기분 수지인 폴리에스테르이미드의 중합반응 시간이 단축될 뿐 아니라 합성된 폴리에스테르이미드 수지는 투명도가 우수하고 밝은 색상인 담황색으로 얻짐을 알 수 있었다.115.7 g of trimellitic anhydride, 59.7 g of methylene dianiline, and 424.2 g of m-cresol were introduced into a 1 L reactor at room temperature, and the reactor was replaced with nitrogen. When the reactor was heated to melt the reaction, stirring was started, and the temperature of the reaction was heated to 150 ° C. over 30 minutes and stirred at 150 ° C. for 1 hour. Thereafter, the temperature of the reactants was increased by 10 ° C. over 30 minutes while removing the water, which was a side reaction product, to obtain a diacid diimide, an intermediate of polyesterimide resin, in a yellow slurry at 180 ° C. 36.9 g of ethylene glycol, 70.5 g of tris (2-hydroxyethyl) isocyanurate, and an organic Ti-P catalyst were added at 0, 200, 400 and 600 ppm relative to the solids of the reactant, and the reaction was heated to 190 ° C. Every 30 minutes thereafter, the temperature was raised to 210 ° C by 10 ° C. Table 2 shows the results of measuring the time at which the reactants change into a clear pale yellow solution while the reaction is continued at 210 ° C. The introduction of the organic Ti-P catalyst in Table 2 not only shortens the polymerization time of the polyesterimide, which is a mood resin used for magnet wire coating, but also shows that the synthesized polyesterimide resin is obtained in pale yellow, which has excellent transparency and light color. Could know.

[표 2]TABLE 2

Ti-P계 촉매량에 따른 중합반응 시간 및 합성된 폴리에스테르이미드의 물성Polymerization Time and Physical Properties of Synthesized Polyesterimide

위 실시예에 의해서 알 수 있는 바와 같이, 본 발명의 효과로는 첫째, 기존의 폴리에스테르이미드 수지 합성에서 사용되어진 촉매보다 반응성이 큰 유기 Ti-P계 촉매를 사용하므로 반응시간 단축과 반응온도 저하의 효과가 있고, 둘째, 유기 Ti-P계 촉매에 열안정제로 작용하는 포스페이트 기가 존재하므로 폴리에스테르이미드 수지 합성시 부반응을 억제할 수 있으며, 셋째, 합성된 폴리에스테르이미드 수지 내에 유기 Ti-P계 촉매가 잔류하므로 폴리에스테르이미드 기본 수지를 다른 첨가제와 혼합하여 마그네트 와이어를 코팅할 때에도 450℃정도의 고열에 견디게 하는 열안정제로서의 역할을 할 수 있고, 넷째, 티타늄 금속이 폴리에스테르이미드 수지에 포함되어 있어 내마모성이 좋아진다.As can be seen by the above embodiment, first, the effect of the present invention is to use the organic Ti-P-based catalyst that is more reactive than the catalyst used in the synthesis of conventional polyesterimide resin, shortening the reaction time and lowering the reaction temperature Second, since there is a phosphate group acting as a thermal stabilizer in the organic Ti-P-based catalyst, side reactions can be suppressed during the synthesis of polyesterimide resin, and third, the organic Ti-P-based resin in the synthesized polyesterimide resin Since the catalyst remains, the polyesterimide base resin can be mixed with other additives to serve as a heat stabilizer that can withstand high heat of about 450 ° C. even when coating the magnet wire. Fourth, titanium metal is included in the polyesterimide resin. There is good wear resistance.

Claims (4)

하기 식으로 나타내지는 폴리에스테르이미드 합성용 유기 Ti-P계 촉매:Organic Ti-P catalyst for polyesterimide synthesis represented by the following formula: TinP O11C14H45 Ti n PO 11 C 14 H 45 상기 식에서, n은 1 내지 3의 정수이다.Wherein n is an integer of 1 to 3. 티타늄 클로라이드(titinium(IV) chloride)를 트리에틸 유기 포스페이트 인산 또는 인산에스테르를 CCI4또는 n-헥센의 촉매 중에서 20 내지 30℃에서 30분간 교반한 후, 다시 30분 동안 에탄올과 반응시킨 다음 에틸렌글리콜을 가함으로써 하기 식으로 나타내지는 폴리에스테르이미드 합성용 유기 Ti-P계 촉매를 제조하는 방법:Titanium chloride (tinium (IV) chloride) was stirred with triethyl organic phosphate phosphoric acid or phosphate ester in CCI 4 or n-hexene catalyst for 30 minutes at 20-30 ° C, and then reacted with ethanol for 30 minutes and then ethylene glycol Process for producing an organic Ti-P catalyst for polyesterimide synthesis represented by the following formula: TinP O11C14H45 Ti n PO 11 C 14 H 45 상기 식에서, n은 1 내지 3의 정수이다.Wherein n is an integer of 1 to 3. 트리멜리트산 무수물과 메틸렌 디아닐린을 m-크레졸 용매중에서 반응시켜 디애시디이미드를 합성한 다음 에틸렌글리콜 및 트리스(2-히드록시에틸) 이소시아누레이트와 함께 하기 식으로 나타내지는 유기 Ti-P계 촉매를 첨가하여 축중합시킴으로써 폴리에스테르이미드를 제조하는 방법:The trimellitic anhydride and methylene dianiline were reacted in m-cresol solvent to synthesize diacidimide, followed by organic Ti-P system represented by the following formula together with ethylene glycol and tris (2-hydroxyethyl) isocyanurate. Process for producing a polyesterimide by adding a catalyst to polycondensation: TinP O11C14H45 Ti n PO 11 C 14 H 45 상기 식에서, n은 1 내지 3의 정수이다.Wherein n is an integer of 1 to 3. 제 3항에 있어서, 유기 Ti-P계 촉매의 함량이 반응물의 고형분 기준으로 200~800 ppm 인 방법.The process according to claim 3, wherein the content of the organic Ti-P catalyst is 200 to 800 ppm based on the solids of the reactants.
KR1019970012437A 1997-03-31 1997-03-31 Organic ti-p catalyst method of its preparation and process for perparing polyester imide using it KR100205699B1 (en)

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Publication number Priority date Publication date Assignee Title
CN114656636A (en) * 2022-04-27 2022-06-24 中瀚新材料科技有限公司 Polyester imide and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114656636A (en) * 2022-04-27 2022-06-24 中瀚新材料科技有限公司 Polyester imide and preparation method thereof
CN114656636B (en) * 2022-04-27 2024-03-26 苏州瀚海新材料有限公司 Polyester imide and preparation method thereof

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