High-performance PBO paper-based material and preparation method thereof
A high-performance, paper-based technology, applied in the pulp beating method, synthetic cellulose/non-cellulose material pulp/paper, papermaking, etc., can solve the problems of stress transfer between interfaces, modulus difference, reduction of PBO dielectric properties, Problems such as heat resistance and ablation resistance, to improve stress transfer, improve poor compatibility, and improve interface interaction
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Embodiment 1
[0035] Preparation of PBO pulp: PBO chopped fibers with a length of 6 mm and a fineness of 2.48 detex were beaten by a Wally beater for 90 min to obtain PBO pulp, and the concentration of the chopped fibers was 1wt%;
[0036] Wet papermaking and sheet forming: Disperse the prepared PBO pulp and chopped fibers in a hydroxyethyl cellulose solution, the chopped fiber content is 40%, the hydroxyethyl cellulose concentration is 0.3 wt%, and the mixture is stirred. After mixing, place it on a rotary screen former to form, and dry at 110 °C after dehydration;
[0037] Preparation of PBO precursor: a certain amount of 2,2-bis(3-amino-4-hydroxyphenyl)hexafluoropropane was dissolved in N,N-dimethylacetamide, cooled to 0 °C, and 4.4 times the molar amount was added. Trimethylchlorosilane and pyridine were heated to room temperature for 30min, then cooled to 0°C, and an equimolar amount of 2,2'-bis(4-formylchlorophenyl)hexafluoropropane was added, and the final solution was 20wt%, The re...
Embodiment 2
[0042] Preparation of PBO pulp: PBO chopped fibers with a length of 1 mm and a fineness of 1 detex are beaten by a Wally beater for 20 minutes to obtain PBO pulp, and the concentration of the chopped fibers is 2wt%;
[0043] Wet papermaking and sheet forming: Disperse the prepared PBO pulp and chopped fibers in a hydroxyethyl cellulose solution, the chopped fiber content is 10%, the hydroxyethyl cellulose concentration is 0.5 wt%, and the mixture is stirred. After mixing, place it on a rotary screen former to form, and dry at 110 °C after dehydration;
[0044]Preparation of PBO precursor: Dissolve a certain amount of 2,2-bis(3-amino-4-hydroxyphenyl)hexafluoropropane in N,N-dimethylacetamide, cool to 0°C, and add 4 times the molar amount Trimethylchlorosilane and pyridine were heated to room temperature for 30min, then cooled to 0°C, and an equimolar amount of 2,2'-bis(4-formylchlorophenyl)hexafluoropropane was added, and the final solution was 5wt%, -20°C for 24h. After wash...
Embodiment 3
[0049] Preparation of PBO pulp: PBO chopped fibers with a length of 10 mm and a fineness of 3 detex are beaten by a Wally beater for 300 minutes to obtain PBO pulp, and the concentration of the chopped fibers is 0.01wt%;
[0050] Wet papermaking and sheet forming: Disperse the prepared PBO pulp and chopped fibers in a hydroxyethyl cellulose solution, the chopped fiber content is 60%, the hydroxyethyl cellulose concentration is 0.01 wt%, and the mixture is stirred. After mixing, place it on a rotary screen former to shape, and dry at 110 °C after dehydration;
[0051] Preparation of PBO precursor: a certain amount of 2,2-bis(3-amino-4-hydroxyphenyl)hexafluoropropane was dissolved in N,N-dimethylacetamide, cooled to 0 °C, and 4.8 times the molar amount was added. The obtained trimethylchlorosilane and pyridine were heated to room temperature for 30 min, then cooled to 0 °C, and an equimolar amount of terephthaloyl chloride was added, the final solution was 30 wt%, and the reacti...
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