Diacetyl cellulose-carbon nano-tube derivatives, preparation method and use thereof
A technology of cellulose diacetate and carbon nanotubes, which is applied in the field of nanomaterials and natural polymers, can solve the problems of natural polymer derivatives - cellulose acetate covalently modified carbon nanotubes research reports, etc., and it is easy to achieve the preparation conditions Satisfaction, rich source of raw materials, and stable chemical structure
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Embodiment 1
[0040] A cellulose diacetate-carbon nanotube derivative with a mass content ratio of cellulose diacetate and carbon nanotubes of about 3.2:1. Reagent reaction, the carboxylic acid group on the surface of the carbon nanotube is converted into a highly reactive acid halide group, and then reacted with a binary functional organic compound to extend the active functional group from the surface of the carbon nanotube, and then react with the trichloro s-triazine reaction to obtain active carbon nanotubes containing chlorotriazine rings that can react with hydroxyl groups on the surface, and finally prepare them through nucleophilic substitution reaction with cellulose diacetate. The specific preparation method is as follows:
[0041] The carbon nanotubes were first pretreated according to the following steps: 15 stainless steel balls with a diameter of 6-8mm and 25g of unpurified carbon nanotubes were placed in two identical 200ml nylon tanks, and then 10ml of non-purified carbon n...
Embodiment 2
[0047] A cellulose diacetate-carbon nanotube derivative with a mass content ratio of cellulose diacetate and carbon nanotubes of about 1.9:1, its specific preparation method is as follows:
[0048] The carbon nanotubes are firstly pretreated, and the pretreatment method is the same as that of the above-mentioned embodiment 1.
[0049] Then take 15 g of pretreated carbon nanotubes and add them to 800 ml of acetone dissolved with 70 g of phosphorus tribromide, stir at 30 ° C for 8 h, and after ultrasonic reaction at 65 ° C for 60 h, centrifuge at a speed of 5000 rpm for 30 min, wash with acetone After cleaning, vacuum-dry at 35° C. for 36 hours to obtain carbon nanotubes with acid halide functional groups on the surface.
[0050] Take 8g of the above-mentioned carbon nanotubes with acid halide functional groups on the surface, add them to 400ml of N-methylpyrrolidone containing 35g of 1,3-propylenediamine and 15ml of triethylamine, stir at 45°C for 6h, After ultrasonic reaction...
Embodiment 3
[0054] A cellulose diacetate-carbon nanotube derivative with a mass content ratio of cellulose diacetate and carbon nanotubes of about 0.6:1, the specific preparation method of which is as follows:
[0055] The carbon nanotubes are firstly pretreated, and the pretreatment method is the same as that of the above-mentioned embodiment 1.
[0056] Then take 1g of the pretreated carbon nanotubes and add it to 50ml of benzene and 50ml of dimethyl dissolved in 1g of thionyl chloride, stir at 30°C for 1h, and after ultrasonic reaction at 30°C for 48h, centrifuge at 3000rpm for 10min , washed with carbon tetrachloride, and vacuum-dried at 30° C. for 24 hours to obtain carbon nanotubes with acid halide functional groups on the surface.
[0057] Take 0.1 g of the above-mentioned carbon nanotubes with acid halide functional groups on the surface, add them to 50 ml of tetrahydrofuran and 50 ml of dimethyl sulfoxide containing 5 g of diethylene glycol and 1 ml of 3-picoline, stir at 30 ° C fo...
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