Preparation method of modified carbon fiber reinforced nylon particle
A fiber-reinforced and modified carbon technology, applied in the field of polymer material science, can solve the problems of low fiber dispersion and damage, and achieve the effects of simple preparation process, uniform distribution, and excellent mechanical properties
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Embodiment 1
[0027] Step 1: Dissolve 10g of hyperbranched polyphenylene ether in 500ml of acetone, immerse 20g of carbon fiber T300 in the above solution, mix ultrasonically at 40°C for 5 hours, and remove the acetone by rotary evaporation to obtain modified carbon fiber;
[0028] Step 2, add 50 parts of nylon 66, 35 parts of modified carbon fiber obtained in step 1 and 15 parts of hyperbranched polyphenylene ether into the mixing equipment, raise the temperature to above 200°C to a molten state, and stir at high speed for 1.5 hours at this temperature; then mix 2 parts γ-glycidyl etheroxypropyltrimethoxysilane, 1 part of inorganic silicon flame retardant, 0.5 part of N,N'-bis-(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propane Acyl)hexamethylenediamine and 0.5 parts of polyethylene wax were added and then continued to stir and mix at high speed for 1h;
[0029] Step 3: Add the obtained mixed material into the twin-screw extruder, control the temperature in the conveying channel within 160°C to ...
Embodiment 2
[0031] Step 1. Dissolve 10g of hyperbranched polyglycidyl ether in 500ml of methanol, immerse 20g of carbon fiber T400 in the above solution, mix ultrasonically at 50°C for 5 hours, and remove methanol by rotary evaporation to obtain modified carbon fiber;
[0032] Step 2, add 60 parts of PA66 / 6, 30 parts of modified carbon fiber prepared in step 1 and 10 parts of hyperbranched polyglycidyl ether into the mixing equipment, raise the temperature to above 200°C to a molten state, and stir at a high speed for 2 hours at this temperature; then put 2 parts of γ-(methacryloyloxy)propyltrimethoxysilane, 1 part of inorganic silicon flame retardant, 2 parts of [β-(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid] After adding pentaerythritol ester and 1 part of zinc stearate, continue to stir and mix at high speed for 1 hour;
[0033] Step 3: Add the obtained mixed material into the twin-screw extruder, control the temperature in the conveying channel within 160°C to 200°C, and extrude...
Embodiment 3
[0035] Step 1: Dissolve 10g of hyperbranched polyphenylene ether in 500ml of acetone, immerse 20g of carbon fiber T600 in the above solution, mix ultrasonically at 40°C for 5 hours, and remove the acetone by rotary evaporation to obtain modified carbon fiber;
[0036] Step 2, add 50 parts of PA610, 35 parts of modified carbon fiber prepared in step 1 and 20 parts of hyperbranched polyphenylene ether into the mixing equipment, raise the temperature to above 200°C to a molten state, stir at high speed for 2 hours at this temperature; then add γ-ammonia 0.5 part of propyltriethoxysilane, 1 part of inorganic silicon flame retardant, 0.5 part of N,N'-bis-(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionyl)hexyl After adding diamine and 1 part of magnesium stearate, continue to stir and mix at high speed for 1 hour;
[0037] Step 3: Add the obtained mixed material into the twin-screw extruder, control the temperature in the conveying channel within 160°C to 200°C, and extrude the materi...
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