Grapheme-containing viscose fiber and preparation method thereof
A viscose fiber and graphene technology, applied in the field of graphene viscose fiber and its preparation process, can solve the problems of short service life, wrinkling, high shrinkage rate of viscose fiber, etc., and achieve the effect of improving the breaking strength
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[0016] A specific preparation method is disclosed, the disclosure of which is incorporated herein by reference.
[0017] In a specific embodiment, specifically, the preparation method of this graphene comprises the steps:
[0018] 1), hydrolyzing corncobs in acid to obtain lignocellulose;
[0019] 2) Treat the lignocellulose with a treating agent at 70°C to 180°C, preferably 90°C to 150°C, and most preferably 100°C to 120°C to obtain porous cellulose. Sulfate, or alkali-sulfite, wherein the acid is preferably sulfuric acid, the base is preferably calcium hydroxide, sodium hydroxide, ammonium hydroxide or magnesium hydroxide, and the sulfite is preferably calcium sulfite, magnesium sulfite, sodium sulfite or ammonium sulfite;
[0020] 3) using ferric chloride, ferrous chloride, ferric nitrate, ferrous nitrate, ferric sulfate, ferrous sulfate, potassium ferricyanide, potassium ferrocyanide, potassium ferrite trioxalate, cobalt chloride, Catalysts of cobalt nitrate, cobalt sul...
Embodiment 1
[0030] Embodiment 1——graphene preparation
[0031] At 90°C, hydrolyze corncobs in sulfuric acid for 10 minutes to obtain lignocellulose, the mass of sulfuric acid is 3% of the mass of corncobs; at 70-180°C, mix with 2:1 sulfuric acid and magnesium sulfite The treating agent treats the lignocellulose to obtain porous cellulose, and the mass of sulfuric acid is 4% of the mass of the lignocellulose. The porous cellulose is bleached with hydrogen peroxide, the mass of the hydrogen peroxide is 5% of the mass of the porous cellulose, the bleaching temperature of the hydrogen peroxide bleaching is 100° C., and the bleaching time is 5 hours.
[0032] Stir the porous cellulose and manganese chloride obtained above at 20°C for 2 hours for catalytic treatment, the mass ratio of manganese chloride and porous cellulose is 0.01:1; drying to obtain a first intermediate product with a water content lower than 10 wt%.
[0033] Put the first intermediate product in the carbonization furnace, ...
Embodiment 2
[0036] Embodiment 2——viscose fiber preparation
[0037] The yellowed cellulose was dissolved in dilute sodium hydroxide solution, and the graphene obtained in Example 1 was added in advance to the dilute sodium hydroxide solution. After ripening, a viscose solution with a solid content of 8% was prepared, stirred with a high-speed mixer for half an hour, and the graphene consumption was 0.6% of the cellulose mass. Filtration, defoaming, and then spinning, desulfurization, washing, and drying to obtain graphene viscose fibers. Wherein, the composition of coagulation bath: sulfuric acid 105g / l, sodium sulfate 200g / l, zinc sulfate 12g / l. The dry breaking strength of the obtained graphene viscose fiber is 8.5cN / dtex, and the wet breaking strength is 2.3cN / dtex.
[0038] The present invention uses the applicant's self-made graphene for the preparation of viscose fiber, which obviously improves the breaking strength of the existing common viscose fiber, and both the dry breaking s...
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