Heat shrinkage-resistant sealing ring and preparation method thereof
A heat-shrinkable sealing and modification technology, applied in the field of sealing rings, can solve the problem that the heat-shrinkage resistance of the seal is difficult to meet the production requirements and so on.
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[0014] The present invention provides a kind of preparation method of heat-shrinkage sealing ring, and this preparation method comprises:
[0015] 1) Contact reaction of polyamide fiber, cyclodextrin, silane coupling agent and water, and then filter and dry the filter cake to obtain modified polyamide fiber;
[0016] 2) Perform solvothermal reaction of modified polyamide fiber, cobalt salt, alkali, urea and ethanol, then filter to take filter cake, and finally calcinate in the presence of protective gas to obtain composite polyamide fiber;
[0017] 3) Mix composite polyamide fibers, shell powder, attapulgite, barium sulfate whiskers, and rare earth oxides to prepare a modified composition;
[0018] 4) Mixing and molding styrene-butadiene rubber, EPDM rubber, fluororubber, talc powder, zinc borate, white carbon black, white oil, aluminum hydroxide, and the modified composition to obtain the heat-resistant Shrink the seal.
[0019] In step 1) of the present invention, the amou...
Embodiment 1
[0035] 1) The polyamide fiber, cyclodextrin, silane coupling agent (vinyl triethoxysilane) and water are subjected to a contact reaction in a weight ratio of 30:13:8:180 (the reaction temperature is 70°C, and the reaction time is 4h), then filter the filter cake and dry it (drying temperature is 110°C, drying time is 5h) to obtain modified polyamide fiber;
[0036] 2) Solvothermal reaction of the modified polyamide fiber, cobalt salt (cobalt nitrate hexahydrate), alkali (sodium hydroxide), urea and ethanol in a weight ratio of 50:12:40:18:200 (reaction temperature 130°C, the reaction time is 12h), then filter to take the filter cake, and finally calcine in the presence of protective gas (helium) (from 18°C at 4.8°C / min to 290°C and hold for 340min, then at 1.8°C / min cooling to 230°C and holding for 1.8h, and finally cooling to 20°C naturally) to make composite polyamide fibers;
[0037] 3) Mix composite polyamide fibers, shell powder, attapulgite, barium sulfate whiskers, ...
Embodiment 2
[0039] 1) Contact reaction of polyamide fiber, cyclodextrin, silane coupling agent (vinyltrimethoxysilane) and water in a weight ratio of 30:10:5:150 (reaction temperature is 65°C, reaction time is 3h ), and then filtered to take the filter cake and dry it (drying temperature is 100°C, drying time is 6h) to obtain modified polyamide fiber;
[0040] 2) Solvothermal reaction of the modified polyamide fiber, cobalt salt (cobalt chloride hexahydrate), alkali (potassium hydroxide), urea and ethanol in a weight ratio of 50:10:30:15:150 (reaction The temperature is 120°C, the reaction time is 16h), then the filter cake is taken by filtration, and finally calcined in the presence of protective gas (nitrogen) (from 15°C at 4.5°C / min to 280°C and kept for 30min, then at 1.5°C / min cooling to 220°C and holding for 1.5h, and finally cooling to 15°C naturally) to make composite polyamide fibers;
[0041] 3) Mix composite polyamide fibers, shell powder, attapulgite, barium sulfate whiskers...
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