A kind of aromatic highly flame-retardant polyester polyol and its preparation method and application
A technology of polyester polyol and aromatic dibasic acid, which is applied in the field of aromatic high flame-retardant polyester polyol and its preparation, can solve the problem of inability to meet the requirements of high flame-retardant performance of building insulation materials and the reduction of physical and mechanical processing performance , migration of flame retardant properties and other issues, to achieve the effects of superior flame retardant performance, good activity and flame retardancy, and high flame retardant performance
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[0026]Preparation method of the present invention mainly comprises the following steps:
[0027] The first step: synthesis of hydroxyl-terminated polyester under the condition of excess alcohol. Add monomer raw materials, catalysts, antioxidants, etc. into the reactor, gradually raise the temperature to 220-240°C, and react for 8-10 hours. In the early stage of the reaction, it is carried out under normal pressure and under the protection of nitrogen. When it reaches the set acid value, hydroxyl value and viscosity range, under reduced pressure, 190-230 ° C, react for 1.5-2 hours, and the reaction can be carried out when the required index is reached. complete. ,
[0028] A novel highly flame-retardant aromatic polyester polyol of the present invention is obtained by esterification of naphthalene-containing aromatic dibasic acids, dibasic acids and small molecule alcohols or acids under the action of catalysts and antioxidants. The average functional group degree is 2, the ...
Embodiment 1
[0041] The preparation of polyester polyol: take by weighing 2,6-naphthalene dicarboxylic acid, terephthalic acid, adipic acid, glycerol, diethylene glycol and catalyst tetraisopropyl titanate according to the proportioning ratio of embodiment 1 in the table , Antioxidants 1010 and 626 were added to the reaction kettle, and nitrogen was introduced for protection, then the temperature was raised, stirred, and gradually raised to 150°C, and after 2 hours of normal pressure reaction, the temperature was programmed to rise to 190°C, and water distillation began When it reaches 240°C, keep it warm for 5 hours. When the water output reaches 80% of the water output, stop feeding nitrogen, cool down to 180°C, start vacuuming in sections, and gradually increase the vacuum degree until the pressure reaches 0.01MPa. Heating while evacuating to raise the temperature to 230° C., and reacting under the above conditions for 1.5 to 2 hours. After testing, the acid value of the product was red...
Embodiment 2
[0043] Take by weighing 2,6-naphthalene dicarboxylic acid, terephthalic acid, adipic acid, glycerol, diethylene glycol and catalyst tetraisopropyl titanate, antioxidant 1010 and 626 Add it into the reaction kettle, and pass it into nitrogen for protection, then start to heat up, stir, and gradually heat up to 150°C. After 2 hours of normal pressure reaction, the temperature is programmed to 180°C, and water begins to distill out. When it reaches 240°C , keep warm for 5 hours, when the water output reaches 75% of the water output, stop feeding nitrogen, cool down to 190°C, start vacuuming in sections, gradually increase the vacuum degree until the pressure reaches 0.01MPa, and heat the temperature while vacuuming. Rise to 240°C, and react under the above conditions for 1.5 to 2 hours. After testing, the acid value of the product was reduced to less than 1mgKOH / g, the reaction was stopped, the temperature was lowered and the material was discharged, and a new type of flame-retar...
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