Polyester polyol as well as preparation method and application
A polyester polyol and polyol technology, applied in the field of polyurethane materials, can solve the problems of long synthesis steps, product flexibility, low temperature resistance and mechanical properties, and increase the difficulty of synthesis process control, so as to improve hardness and synthesis Simple method, convenient and efficient synthetic route
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2020-01-24
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Abstract
Description
technical field
[0001] The invention relates to a polyester polyol, in particular to a polyester polyol, a preparation method and application, and belongs to the technical field of polyurethane materials. Background technique
[0002] Urethane acrylate is an important class of photocurable cross-linked polyurethane resin. It is based on polyurethane, and the end of the molecular chain introduces double bonds through acrylation. bond crosslinking reaction. Its molecular structure mainly includes a urethane segment, a polyol main chain, and an acrylate hydroxyalkyl ester segment, and the curing characteristics are determined by the acrylate located in the segment. Urethane acrylates combine the advantages of both acrylic and polyurethane resins.
[0003] The polymerizable double bonds of urethane acrylate oligomers are generally located at the end of the molecular chain. In order to increase the double bond content of photocurable urethane acrylate, improve the curing rate a...
Examples
Embodiment 1-12
[0052] A kind of preparation method of polyester polyol, the raw material that adopts and proportioning reference table 1;
[0053] The overall preparation process is: in a 5L stainless steel reaction kettle equipped with heating jacket, stirring, nitrogen stripping, rectification tower, vacuum gauge, and alcohol recovery tank, according to Table 1, components A, B, C and polymerization inhibition agent. Heat up to 145°C to melt and start the reaction. As the reaction progresses, the by-product water is continuously separated from the system, and the reaction stage lasts for 1 hour. Subsequently, the temperature was further raised to 250° C. for 3 hours. After 1 hour of heat preservation at 250°C, the reaction water gradually slowed down. At this time, tetra-n-butyl titanate was added, and the vacuum degree was increased to 0.09MPa within 1 hour to continue the reaction. The reaction stops when the value reaches the set value. Cool down to 150°C, discharge and pack. The ob...