Polyamine monomer of polyimide containing triazole structure and polymer and preparation method of polyamine monomer as well as application
A polyimide and polyamine technology, which is applied in the field of hyperbranched polyimide preparation technology and information storage materials, can solve problems such as difficult processing, poor solubility, and difficult modification
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Embodiment 1
[0064] Taking triamine monomer as an example, the preparation steps of polyamine monomer are described. The specific synthesis route and steps are as follows:
[0065]
[0066] The first step reaction: under nitrogen protection, add 120mmol (26.4g) 4-bromobenzoyl chloride to a 250mL three-necked flask, then add 120mL N-methylpyrrolidone (NMP), and place the entire reaction system in an ice-water bath , cooled to 0°C. Under the condition of mechanical stirring, add 80 mmol (3.8 mL) hydrazine hydrate into the three-necked flask with a constant pressure dropping funnel in about 30 minutes. Continue the reaction at 0°C for 60 minutes, then remove the ice-water bath, stir at room temperature at about 20-25°C, and continue the reaction for 12 hours. After the reaction is completed, the material is discharged in 1000-2000 mL of distilled water, filtered, and the filter cake is washed 3-5 times with distilled water, and then washed 2-3 times with ethyl acetate. Put the filter cak...
Embodiment 2
[0072] Taking triamine monomer and hexafluorodianhydride as examples, the synthesis of acid anhydride-terminated hyperbranched polyimide is illustrated. The specific synthesis route and steps are as follows:
[0073]
[0074] (1) Weigh 0.342g of triamine monomer and place it in a constant pressure dropping funnel, dissolve it with 8.0ml N,N-dimethylacetamide (DMAc) at room temperature; weigh 0.888g of 6FDA and add it to three Neck flask, dissolved with 10ml DMAc;
[0075] (2) Under nitrogen atmosphere and mechanical stirring conditions, the triamine monomer completely dissolved in the constant pressure funnel was slowly added into the three-necked flask dissolved in the anhydride solution within two hours, stirred at room temperature for 24 hours, and overspending Polyamic acid;
[0076] (3) Add 3ml of acetic anhydride and 1ml of pyridine to the system, keep the oil bath at a constant temperature of 80°C, and perform chemical imidization for 12 hours to obtain a hyperbranche...
Embodiment 3
[0080] In this embodiment, taking the hyperbranched polyimide obtained in Example 2 as an example, the preparation process of the storage device with the ITO / hyperbranched polyimide active layer / Al structure is described, as follows:
[0081] First, wash the ITO glass bottle with detergent water, deionized water, ultrapure water, acetone, and isopropanol under ultrasonic conditions for 25 minutes, and put the cleaned ITO glass piece in a vacuum oven at 80°C Dry for 5 hours. Weigh 20 mg of hyperbranched polyimide and dissolve it in 1 mL of anhydrous N,N-dimethylacetamide, and stir evenly. After filtering the solution with a 0.22 μm organic filter head, drop 3 to 4 drops of the solution on a clean and dry ITO glass sheet, and use a spin coater to rotate at a low speed of 200r / min for 20s to make the solution on the ITO glass. Distribute evenly on the board, then increase the rotation speed to 1000r / min, rotate for 30s, transfer to a preheated 40°C vacuum oven, dry at 40°C for 6...
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