A kind of anti-thermal shock conductive polyimide fiber and preparation method thereof
A technology of polyimide fiber and thermal shock resistance, which is applied in fiber types, fiber processing, textiles and papermaking, etc., and can solve problems such as limiting the application of high-performance fibers and poor thermal shock resistance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0046] The present invention provides a method for preparing thermal shock-resistant conductive polyimide fibers described in the above technical solution, comprising the following steps:
[0047] Alkaline treatment and cleaning of the polyimide fibers to obtain polyimide fibers containing carboxylate on the surface;
[0048] The polyimide fiber containing carboxylate on the surface is reacted in a solution of pyridine derivative or quinoline derivative, and washed to obtain polyimide fiber containing pyridine derivative or quinoline derivative on the surface;
[0049] placing the polyimide fibers containing pyridine derivatives or quinoline derivatives on the surface in a soluble metal salt solution to complex metal ions to obtain polyimide fibers containing metal ions on the surface;
[0050] The polyimide fiber containing metal ions on the surface is reduced and cleaned to obtain the polyimide fiber with a composite metal transition layer on the surface;
[0051] The polyi...
Embodiment 1
[0070] Pyridine derivatives of formula 102: Dissolve 2-aminopyridine (47.0g, 0.5mol) and triethylamine (104.2mL, 0.75mol) in dichloromethane (300.0mL), and control the reaction temperature at 0°C to 20°C 2-Chloroacetyl chloride (62.1 g, 0.55 mol) was added dropwise at ℃, and reacted at room temperature for 3 h after the drop was completed. Add water (100.0 mL) and continue stirring for 1 h, separate the water phase, wash the organic phase with saturated aqueous sodium bicarbonate (100.0 mL), dry the organic phase with anhydrous sodium sulfate, filter off the desiccant, distill off dichloromethane, and dry in vacuo A reddish solid was obtained (76.8 g, yield: 90%). 1 H NMR (400MHz, CDCl 3 ):δ4.20(s,2H),7.10–7.09(m,1H),7.77–7.72(m,1H),8.20(d,1H,J=4.4Hz),8.32–8.31(m,2H), 8.93(s,1H).
Embodiment 2
[0072] Pyridine derivatives with the structure of formula 103: using 3-aminopyridine as the reaction raw material, the preparation process is the same as that of formula 102, the product is a white solid, the yield: 80.2 g, the yield: 94%. 1 H NMR (400MHz,D 2 O): δ9.16(d, J=3Hz, 1H), 8.42(d, 1H, J=6Hz), 8.40(d, 1H, J=9Hz), 7.90(dd, 1H, J=9Hz, 6Hz) ,4.25(s,2H).
PUM
| Property | Measurement | Unit |
|---|---|---|
| electrical conductivity | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 


