Method for preparing liquid ethylene based polysilazane resin by UV initiated vinyl silazane rapid polymerization

A vinyl polysilazane and vinyl silazane technology, which is applied to the synthesis field of liquid vinyl polysilazane, can solve the problems of high reaction temperature, difficult reaction control, slow reaction rate and the like, and avoids thermal polymerization. Effect

Inactive Publication Date: 2009-01-28
NORTHWESTERN POLYTECHNICAL UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

One is the addition reaction of Si-H, N-H and vinyl double bonds on the molecular chain at high temperature (generally 280-300°C). Although the synthesis rate of this polymerization reaction is relatively fast (tens of Minutes), but due to the high reaction temperature, the reaction is difficult to control; the other is to use a platinum catalyst to perform thermal polymerization at 50-90°C. Although this type of reaction avoids the disadvantages of high thermal polymerization temperature and difficult control of the reaction, However, there are still defects such as slow reaction rate and long synthesis cycle, and the reaction time generally needs more than 8 hours

Method used

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  • Method for preparing liquid ethylene based polysilazane resin by UV initiated vinyl silazane rapid polymerization
  • Method for preparing liquid ethylene based polysilazane resin by UV initiated vinyl silazane rapid polymerization

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] Formula 1: 0.5 mol (70.5 g) of methylvinyldichlorosilane, 0.15 mol (17.3 g) of methylhydrogendichlorosilane, 500.0 g of organic solvent n-hexane, and 0.04 g of platinum diacetylacetonate.

[0023] Synthesis process: Add the raw materials methylvinyldichlorosilane, methylhydrogendichlorosilane and n-hexane according to the ratio into a 1000mL four-neck flask equipped with a thermometer and a stirrer, put it in an ice-water bath to cool to -5°C, and start The mixer mixes the ingredients well. Then feed ammonia gas at a flow rate of 15-20L / h, and react for 2.5 hours. After the ammonia gas flow was stopped, the ice bath was removed. After the reaction returned to room temperature, the product was filtered to remove the generated salt. The filtrate was heated (not exceeding 90°C) and n-hexane was removed under reduced pressure, and the solvent was collected for recycling. When no solvent comes out, stop heating and vacuuming, lower to room temperature, add platinum diacetyl...

Embodiment 2

[0027] Formula 2: 0.5 mol (70.5 g) of methylvinyldichlorosilane, 0.2 mol (23.0 g) of methylhydrogendichlorosilane, 600.0 g of n-hexane, and 0.04 g of platinum diacetylacetonate.

[0028] Synthesis process: Add the raw materials methylvinyldichlorosilane, methylhydrogendichlorosilane and n-hexane according to the ratio into a 1000mL four-necked flask equipped with a thermometer and a stirrer, put it in an ice-water bath to cool to 0°C, and start stirring Mix the ingredients evenly. Then feed ammonia gas at a flow rate of 15-20L / h, and react for 2.5 hours. After the ammonia gas flow was stopped, the ice bath was removed. After the reaction returned to room temperature, the product was filtered to remove the generated salt. The filtrate was heated (not exceeding 90°C) and n-hexane was removed under reduced pressure, and the solvent was collected for recycling. When no solvent comes out, stop heating and vacuuming, lower to room temperature, add platinum diacetylacetonate catalys...

Embodiment 3

[0033] Formula 3: 0.5 mol (70.5 g) of methylvinyldichlorosilane, 0.15 mol (17.3 g) of methylhydrogendichlorosilane, 600.0 g of cyclohexane, and 0.04 g of platinum diacetylacetonate.

[0034] Synthesis process: Add the raw materials methylvinyldichlorosilane, methylhydrogendichlorosilane and n-hexane according to the ratio into a 1000mL four-necked flask equipped with a thermometer and a stirrer, put it in an ice-water bath to cool to 2°C, and start stirring Mix the ingredients evenly. Then feed ammonia gas at a flow rate of 15-20L / h, and react for 2.5 hours. After the ammonia gas flow was stopped, the ice bath was removed. After the reaction returned to room temperature, the product was filtered to remove the generated salt. The filtrate was heated (not exceeding 90°C) and n-hexane was removed under reduced pressure, and the solvent was collected for recycling. When no solvent comes out, stop heating and vacuumize, lower to room temperature, add platinum diacetylacetonate cat...

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Abstract

The invention relates to a method for preparing liquid vinyl poly-silazane resin by fast polymerization of vinyl poly-silazane initiated by UV light, and the technique thereof is characterized by comprising the following steps: methyl vinyl dichlorsilane, methyl hydrogen dichlorsilane and an organic solvent are added into a flask, and then put the flask in a water-ice bath for evenly mixing; ammonia gas is introduced for reaction; after the introduction of the ammonia gas is stopped, the ice-water bath is removed and after the reaction is restored to room temperature, resultant is filtered; then filtrate is heated and decompressed for removing normal hexane, and when no solvent is generated, heating is stopped, vacuum-pumping is carried out and temperature is reduced to the room temperature; a diacetyl acetone platinum catalyst is added and then dissolved by stirring; an ultraviolet lamp is turned on for irradiation and finally a transparency liquid of colorless to light yellow is obtained. The vinyl poly-silazane resin prepared by the method of the invention has the advantages that: the yield thereof can achieve 44-50 percent of the input amount of chlorsilane, viscosity is within 300-2000mPa question mark s, and the analysis of gel permeation chromatography (GPC) shows that the M of the synthesized vinyl poly-silazane resin can be up to 4200, and the molecular weight dispersion coefficient thereof is within 1.6-4.0.

Description

technical field [0001] The invention relates to a method for preparing liquid vinyl polysilazane tree through rapid polymerization of vinyl silazane induced by ultraviolet light, which belongs to the synthesis method of liquid vinyl polysilazane. Background technique [0002] Silicon nitride and silicon carbide ceramic materials can be prepared by pyrolysis conversion method using polymer ceramic precursors containing silicon, nitrogen and (or) carbon elements. The preparation of ceramic materials by this method has the advantages of adjustable composition of silazane (carbon) alkane precursors, and can be shaped by general polymer processing methods. It has broad application prospects in the fields of aerospace thermal protection, ceramic fiber, and connection of ceramic structural parts. [0003] Currently used polysilazane resins containing active groups (such as vinyl, etc.) are mainly prepared by thermal polymerization, and there are two commonly used synthetic methods...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C08G77/62
Inventor 陈立新宋家乐
Owner NORTHWESTERN POLYTECHNICAL UNIV
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