A kind of low-viscosity bio-based epoxy resin based on vanillin and preparation method thereof
A technology based on epoxy resin and vanillin, which is applied in the field of low-viscosity bio-based epoxy resin and its preparation, can solve the problems of unstable performance, difficult application, poor resin processing performance, etc., achieve low-viscosity thermodynamic properties, improve cross-linking The effect of improving joint density and mechanical properties
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[0034] The present invention also provides a kind of preparation method of low-viscosity bio-based epoxy resin based on vanillin, comprising the following steps:
[0035] Step 1. Under nitrogen protection, add solvent, glycerin, itaconic acid and methanesulfonic acid into the reaction vessel, and then react at 140-160°C for 5-10 hours. The molar ratio of glycerol to itaconic acid is preferably 1:3-5, the quality of catalyzer methanesulfonic acid is 0.15wt%; The selected solvent is preferably toluene, and reaction route is as follows:
[0036]
[0037] Step 2: Add product 1, solvent and DMF to the reaction vessel and place it in an ice-water bath at 0°C for stirring. The stirring rate is preferably 300-400r / min, then drop in oxalyl chloride, slowly heat the reaction mixture and set it at 20- React at 70°C for 3-5 hours until the solid is completely dissolved, and then rotate the obtained solution preferably at 40-60°C to obtain product 2; the molar ratio of the product 1 to ...
Embodiment 1
[0046] Step 1. Add 0.3mol powdered itaconic acid, 0.1mol glycerin, 50ml toluene, and 5wt% catalyst methanesulfonic acid into a three-neck round bottom flask, one of which is equipped with a stirrer and the other for nitrogen flow, a third neck toluene reflux and azeotropic distillation apparatus, the internal temperature was set to 150 °C and the reaction was continued for 10 hours. From toluene, gradually extract the condensed release water (1.5mol); Anhydrous toluene is continuously refluxed in the reactor to obtain product 1; the nuclear magnetic spectrum is as figure 2 shown.
[0047] Step 2. Add the mixture of product 1 (0.1mol), THF (100ml) and DMF (catalyst, 0.05ml) to a round-bottomed flask, and add oxalyl chloride (0.3mol) drop by drop within 20min in an ice-water bath at 0°C . The reaction mixture was slowly heated and reacted at 50 °C for 4 hours until the solid was completely dissolved. The resulting solution was then rotatably steamed to obtain product 2;
[...
Embodiment 2
[0059] Step 1. Add 0.5mol powdered itaconic acid, 0.1mol glycerol, 50ml toluene, and 5wt% catalyst methanesulfonic acid into a three-neck round bottom flask, one of which is equipped with a stirrer and the other for nitrogen flow, a third neck toluene reflux and azeotropic distillation apparatus, set the internal temperature to 160 °C and continue the reaction for 5 hours. Condensed liberated water (1.5 mol) was gradually extracted from toluene; anhydrous toluene was continuously refluxed into the reactor to obtain product 1;
[0060] Step 2. Add the mixture of product 1 (0.1mol), THF (100ml) and DMF (catalyst, 0.05ml) to a round-bottomed flask, and add oxalyl chloride (0.4mol) drop by drop within 20min in an ice-water bath at 0°C . The reaction mixture was slowly heated and reacted at 25°C for 4 hours until the solid was completely dissolved. The resulting solution was then rotatably steamed to obtain product 2;
[0061] Step 3, add product 2 (0.1mol) into 100ml ethyl acet...
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