Method for compounding functional nanoparticles on surfaces of polymer filaments
A technology of functional nanoparticles and surface compounding, which is applied in the field of new fiber materials, can solve problems affecting product performance, large-scale application limitations, and difficulty in dispersing, and achieve excellent mechanical properties, compatibility, and good compatibility.
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[0036] Preparation of B blend solution
[0037] According to the following mass percentage:
[0038] Surface proteinized functional nanoparticles 1-16%
[0039] Thermoplastic Polyurethane 1-12%
[0040] Dimethylformamide 72-98%
[0041] Put the surface proteinized functional nanoparticles prepared by step A into dimethylformamide, and after ultrasonic dispersion for 1-3h, add thermoplastic polyurethane with a number average molecular weight of 20000-180000 and a melting point of 160-190°C, Under the condition that the temperature is 25-35°C, mechanical stirring is used to dissolve the thermoplastic polyurethane. After dissolving for 3-5 hours, a blended solution is obtained through static vacuum degassing. The viscosity of the blended solution is 500-2000mPa·s. The vacuum defoaming temperature is 25-35°C;
[0042] Formation and Thickness Control of Composite Blend Solution on the Surface of C Polymer Filaments
[0043] Warm up the blended solution prepared in step B to 35...
Embodiment 1
[0050] A Protein modification of the surface of functional nanoparticles
[0051] Adopt ultrasonic wave to be that the carbon nanotube 5g that average particle diameter is 20nm is dispersed in the keratin aqueous solution 100g that mass fraction is 0.5%, the number-average molecular weight of keratin is 1000, and dispersion temperature is 50 ℃, after dispersing 1h, will disperse solution The temperature was lowered to 1 ° C, and after standing still for 24 hours, centrifuged and dried to obtain surface proteinized carbon nanotubes, the centrifugal speed of the centrifuge was 5000 rpm, and the drying temperature was 80 ° C;
[0052] B put 1 g of surface proteinized carbon nanotubes prepared in step A into 98 g of dimethylformamide, and after ultrasonic dispersion for 1 h, add 1 g of thermoplastic polyurethane with a number average molecular weight of 20,000 and a melting point of 160° C. Under the condition of 25°C, the thermoplastic polyurethane was dissolved by mechanical sti...
Embodiment 2
[0057] A Protein modification of the surface of functional nanoparticles
[0058] Adopt ultrasonic wave to be that the graphene 6g that average particle diameter is 50nm is dispersed in the silk fibroin aqueous solution 100g that mass fraction is 0.8%, the number-average molecular weight of silk fibroin is 2000, and dispersion temperature is 55 DEG C, disperse 2h after the temperature of dispersion solution Be reduced to 2 DEG C, after standing still for 36h, obtain surface proteinized graphene through centrifuge centrifugation and drying, the centrifugal speed of centrifuge is 5000 rev / min, and drying temperature is 80 DEG C;
[0059] B puts the surface proteinized graphene 2g prepared by step A into 97g dimethylformamide, after adopting ultrasonic dispersion for 2h, adding number-average molecular weight is 300000, melting point is 170 DEG C of thermoplastic polyurethane 1g, at a temperature of Under the condition of 30°C, the thermoplastic polyurethane was dissolved by mech...
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