Hyperbranched ester compound and nylon fiber-added composite material and preparation method thereof
A technology of ester compounds and composite materials, which is applied in the field of hyperbranched ester compounds and nylon fiber-reinforced composite materials and their preparation, and can solve the problem of high roughness
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[0034] Among the present invention, the preparation method of described hyperbranched ester compound comprises the following steps:
[0035] (1) carry out ring-opening polymerization reaction with the hydroxy epoxy group phenol compound of structure shown in formula (I) in the presence of initiator, obtain polyhydroxyl hyperbranched precursor;
[0036] (2) Polycondensing polyhydroxy hyperbranched precursors and special hindered carboxylic acids having a structure shown in formula (II) under the catalytic action of an esterification catalyst to obtain hyperbranched ester compounds;
[0037]
[0038] In formula (I), m is an integer of 1-10, such as 1, 2, 3, 4, 5, 6, 7, 8, 9, 10. m is preferably an integer of 1-5, most preferably 1. When m is 1, the hydroxy epoxy phenolic compound is 4-(2-hydroxyl-4-(oxirane-2-alkyl) butyl) phenol, and its structural formula is as shown in formula (III) ;
[0039]
[0040] In formula (II), n is an integer of 0-10, such as 0, 1, 2, 3, 4, ...
preparation example 1
[0067] Preparation Example 1 This preparation example is used to illustrate the preparation of hyperbranched ester compounds
[0068] (1) Take 100 g of 4-(2-hydroxy-4-(oxirane-2-alkyl) butyl) phenol that has been dehydrated and deoxygenated in a Schlenk bottle, add 5 g potassium tert-butoxide, 5 g tert-butoxide Butanol and 50g tetrahydrofuran were reacted for 10h at a temperature of 50°C and a pressure of 0.25MPa under a nitrogen atmosphere to obtain a polyhydroxy hyperbranched precursor;
[0069] (2) Add 100g of polyhydroxy hyperbranched precursor and 600g of 5-hydroxy-3,4-diphenylpentanoic acid into a Schlenk bottle respectively, add 6g of concentrated sulfuric acid, and react at a temperature of 180°C and a pressure of 0.1MPa for 2h, Obtain hyperbranched ester compound, denoted as CZ-1.
preparation example 2
[0070] Preparation Example 2 This preparation example is used to illustrate the preparation of hyperbranched ester compounds
[0071] (1) Take 100 g of 4-(2-hydroxy-4-(oxirane-2-alkyl) butyl) phenol that has been dehydrated and deoxygenated in a Schlenk bottle, add 5 g potassium tert-butoxide, 5 g tert-butoxide Butanol and 50g tetrahydrofuran were reacted for 30h at a temperature of 60°C and a pressure of 0.25MPa under a nitrogen atmosphere to obtain a polyhydroxyl hyperbranched precursor;
[0072] (2) Add 100g of polyhydroxy hyperbranched precursor and 500g of 5-hydroxy-3,4-diphenylpentanoic acid into a Schlenk bottle, add 6g of concentrated sulfuric acid, and react at a temperature of 100°C and a pressure of 0.25MPa for 0.5h , to obtain hyperbranched ester compounds, denoted as CZ-2.
[0073] Preparation Example 3 This preparation example is used to illustrate the preparation of hyperbranched ester compounds
[0074](1) Take 100 g of 4-(2-hydroxy-4-(oxirane-2-alkyl) butyl)...
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