Synthesis method of self-repairing elastomer material based on eucommia rubber
A technology of elastomer materials and synthesis methods, applied in the field of synthesis of self-healing elastomer materials, can solve problems such as difficult to be repaired in time, macro cracks, material failure, etc., and achieve low-cost raw materials, easy-to-obtain raw materials, and mature process routes Effect
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Embodiment 1
[0023] Add 10 g of eucommia gum to 120 ml of petroleum ether, raise the temperature to 42°C until completely dissolved, continue to add 100 ml of deionized water and stir to obtain a stable emulsion of eucommia gum. To this was added 6 ml of formic acid and H 2 o 2 20 ml, and epoxidation reaction at 42°C for 5h. After the epoxidation reaction, the emulsion system was adjusted to pH=5 with 10% aqueous sodium hydroxide solution, and 5 ml of methyltriethoxysilane, 10.0 ml of formic acid, and 5 ml of absolute ethanol were added to continue the reaction for 3 h. The product was precipitated by absolute ethanol, washed, and dried in vacuo to constant weight.
Embodiment 2
[0025] Add 20 g of eucommia gum to 260 ml of cyclohexane, raise the temperature to 60°C until completely dissolved, continue to add 150 ml of deionized water and stir to obtain a stable emulsion of eucommia gum. To this was added 6 ml of formic acid and H 2 o 2 30ml, epoxidation reaction 2 h. After the epoxidation reaction, the pH of the system was adjusted to 9 with ammonia water. A solution made of 6 ml dichlorodimethylsilane, 12 ml absolute ethanol, 12 ml deionized water and 0.3 ml hydrochloric acid was added dropwise at a constant speed, and the reaction was continued for 2 h after the addition was completed. The product was precipitated by absolute ethanol, washed, and dried in vacuo to constant weight.
Embodiment 3
[0027] Dissolve 20 g of Eucommia gum in 260 ml of cyclohexane, raise the temperature to 50°C until completely dissolved, continue to add 150 ml of deionized water and stir to obtain a stable emulsion of Eucommia gum. To this was added 10 ml of formic acid and H 2 o 230 ml, and epoxidized at 50°C for 3 h. After the epoxidation reaction, the pH of the system was adjusted to 4 with 10% aqueous sodium hydroxide solution. 8 ml of 3-aminopropyltrihydroxysilane, 26 ml of formic acid, 10 ml of absolute ethanol, and 10 ml of deionized water were successively added thereto, and the reaction was continued for 2 h. The product was precipitated by absolute ethanol, washed, and dried in vacuo to constant weight.
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