Polyamide film with electrochromism performance, and preparation method and application thereof
A polyamide film, electrochromic technology, applied in the direction of color-changing fluorescent materials, chemical instruments and methods, chemical recycling, etc., can solve the problems of poor thermal stability, low solubility of polyamide, difficult to process into film, etc. , good reversibility, good high temperature performance effect
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specific Embodiment approach 1
[0056] Specific implementation mode one: the present implementation mode is a polyamide film with electrochromic properties. The structural formula is:
[0057] Wherein, the R is The value of n is 1≤n≤100, and n is an integer.
[0058] The advantage of this implementation mode:
[0059] 1. The polyamide film with electrochromic properties prepared in this embodiment is dissolved in dimethyl sulfoxide, and can be coated on conductive glass; the polyamide film with electrochromic properties prepared in this embodiment is used as The working electrode, the saturated calomel electrode is the reference electrode, the platinum wire is the counter electrode, and the electrolyte is an electrochromic device composed of lithium perchlorate acetonitrile solution;
[0060] 2. The polyamide film with electrochromic properties prepared in this embodiment loses 5% of its weight at a temperature of 340°C to 410°C, 10% at a temperature of 350°C to 450°C, and 32% at a temperature of 700°...
specific Embodiment approach 2
[0064] Specific embodiment two: this embodiment is a kind of preparation method of the polyamide film with electrochromic performance is prepared according to the following steps:
[0065] 1. Synthesis of N,N'-bis(α-naphthyl)-N,N'-bis(4-isocyanatophenyl)biphenyl monomer:
[0066] 1. Dissolve N,N-bis(1-naphthyl)-4,4-biphenyldiamine in dimethyl sulfoxide under nitrogen atmosphere, then add p-fluoronitrobenzene and sodium hydride, and then React at ℃ for 24h-30h to obtain a reaction solution; add the reaction solution to cold water, then perform suction filtration, discard the filtrate, and obtain a yellow precipitate; use acetonitrile to wash the yellow precipitate for 2 to 4 times, and then in the temperature Dry at 30°C to 40°C for 8 to 15 hours to obtain reaction product A; the reaction product of N,N-bis(1-naphthyl)-4,4-biphenylenediamine and p-fluoronitrobenzene described in step ① The amount ratio of substances is 1:2;
[0067] The volume ratio of the amount of N,N-bis(1...
specific Embodiment approach 3
[0086] Specific embodiment three: the difference between this embodiment and specific embodiment two is: the organic solvent described in step two is one of triphenyl phosphite, pyridine and N-methylpyrrolidone or a mixture of several of them . Others are the same as in the second embodiment.
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