Preparation method of permeable reinforced raw silk processing agent
A treatment agent and enhanced technology, applied in fiber treatment, chemical instruments and methods, textiles and papermaking, etc., can solve the problems of small increase in breaking strength of raw silk, poor air permeability of fabrics, and difficult treatment of wastewater, and achieve application effects. Good, antistatic and flame retardant properties are improved, and the effect of improving air permeability
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[0020] 1. A method for preparing a water-permeable enhanced raw silk treatment agent, characterized in that:
[0021] Achieved by the following steps:
[0022] Step 1: Preparation of graphene oxide:
[0023] 6 parts by weight of graphite powder with a particle size less than 30 microns, 3 parts by weight of sodium nitrate and 60 parts by weight of concentrated sulfuric acid are stirred and mixed evenly in an ice bath environment and slowly add 16 parts by weight of potassium permanganate; then the mixture is transferred React in a water bath at 35°C for 30 minutes, gradually add 280 parts by weight of deionized water, then raise the temperature to 68°C and continue the reaction for 4 hours; then add 20 parts by weight of hydrogen peroxide solution with a mass fraction of 30% dropwise, and adjust the pH= 6. Ultrasonic treatment for 30 minutes, centrifugal filtration, and vacuum drying at 50°C to obtain graphene oxide;
[0024] Step 2: Amino-modified graphene oxide:
[0025] ...
Embodiment 1
[0030] Step 1: Preparation of graphene oxide:
[0031] 6 parts by weight of graphite powder with a particle size less than 30 microns, 3 parts by weight of sodium nitrate and 60 parts by weight of concentrated sulfuric acid are stirred and mixed evenly in an ice bath environment and slowly add 16 parts by weight of potassium permanganate; then the mixture is transferred React in a water bath at 35°C for 30 minutes, gradually add 280 parts by weight of deionized water, then raise the temperature to 68°C and continue the reaction for 4 hours; then add 20 parts by weight of hydrogen peroxide solution with a mass fraction of 30% dropwise, and adjust the pH= 6. Ultrasonic treatment for 30 minutes, centrifugal filtration, and vacuum drying at 50°C to obtain graphene oxide;
[0032] Step 2: Amino-modified graphene oxide:
[0033] 3 parts by weight of graphene oxide, 60 parts by weight of N,N-dimethylformamide, 5 parts by weight of ethylenediamine and 1 part by weight of dicyclohexyl...
Embodiment 2
[0037] Step 1: Preparation of graphene oxide:
[0038] 6 parts by weight of graphite powder with a particle size of less than 30 microns, 3 parts by weight of sodium nitrate and 60 parts by weight of concentrated sulfuric acid are stirred and mixed evenly in an ice bath environment and slowly add 16 parts by weight of potassium permanganate; then the mixture is transferred React in a water bath at 35°C for 30 minutes, gradually add 280 parts by weight of deionized water, then raise the temperature to 68°C and continue the reaction for 4 hours; then add 20 parts by weight of hydrogen peroxide solution with a mass fraction of 30% dropwise, and adjust the pH= 6. Ultrasonic treatment for 30 minutes, centrifugal filtration, and vacuum drying at 50°C to obtain graphene oxide;
[0039] Step 2: Amino-modified graphene oxide:
[0040] 3 parts by weight of graphene oxide, 60 parts by weight of N,N-dimethylformamide, 10 parts by weight of ethylenediamine and 2 parts by weight of dicyclo...
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