Self-plasticized fluoropolymer lithium ion conductor, its preparation method and application
A polymer, self-plasticizing technology, applied in the field of polymer material technology and lithium batteries, can solve the problems of dispersion and interaction between polyoxyethylene materials and lithium salts that are rarely considered
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Embodiment 1
[0050] In this embodiment, the fluorine-containing polymer lithium ion conductor is a fluorine-containing polyetheretherketone resin (Li type) with side chain grafted PEGMe2000, and its synthetic reaction route is as follows figure 1 As shown, the details are as follows:
[0051] Step 1: Synthesis of potassium salt of p-carboxybenzenesulfo-(5-iodo-3-oxa-octafluoropentyl)sulfonylimide (ICF 2 CF 2 OCF 2 CF 2 SO 2 NKSO 2 ArCOOH)
[0052] Add 50ml of deionized water, 0.01mol of p-carboxybenzenesulfonamide, 0.02mol of potassium hydroxide, and 0.01mol of potassium carbonate into a 250ml three-necked flask, and mix well; when the temperature returns to room temperature, add 0.0005mol of octadecadecrown ether, stir and dissolve , 50 ml of toluene solution in which 0.01 mol of 5-iodo-3-oxa-octafluoropentylsulfonyl fluoride monomer was dissolved was added dropwise, and reacted for 0.5 hmin under stirring at 1000 rpm.
[0053] The reaction product was separated from the water phas...
Embodiment 2
[0063] Step 1: Synthesis of (4-potassium carboxylate-3-oxa-hexafluorobutyl)-sulfo-(5-iodo-3-oxa-octafluoropentyl)sulfonylimide potassium salt (ICF 2 CF 2 OCF 2 CF 2 SO 2 NKSO 2 CF 2 CF 2 OCF 2 COOK)
[0064] Add 50ml acetonitrile in 250ml there-necked flask, 0.01mol4-carboxy-3-oxa-hexafluorobutylsulfonamide (N 2 SO 2 CF 2 CF 2 OCF 2 COOH), 0.04mol of anhydrous potassium carbonate were mixed uniformly and heated to 60°C, and 0.01mol of 5-iodo-3-oxa-octafluoropentylsulfonyl fluoride monomer (ICF 2 CF 2 OCF 2 CF 2 SO 2 F) Reaction for 6h.
[0065] After the mixture was filtered, the mother liquor was rotary evaporated to remove acetonitrile, and the obtained yellow-white solid was recrystallized with deionized water to obtain the product ICF 2 CF 2 OCF 2 CF 2 SO 2 NKSO 2 CF 2 CF 2 OCF 2 COOK.
[0066] Step 2: Synthesis of fluorine-containing sulfonimide grafted polysulfone with carboxyl groups
[0067] Dissolve 5g of polysulfone with a bromine content ...
Embodiment 3
[0075] Step 1: Synthesis of potassium salt of (4-carboxymethyl-3-oxa-hexafluorobutyl)-sulfo-(5-iodo-3-oxa-octafluoropentyl)sulfonylimide (ICF 2 CF 2 OCF 2 CF 2 SO 2 NKSO 2 CF 2 CF 2 OCF 2 COOCH 3 )
[0076] Add 50ml acetonitrile in 250ml there-necked flask, 0.01mol4-carboxy-3-oxa-hexafluorobutylsulfonamide (H 2 NSO 2 CF 2 CF 2 OCF 2 COOCH 3 ), 0.04mol of anhydrous potassium carbonate, mix uniformly and heat up to 60°C, add 0.01mol of 5-iodo-3-oxa-octafluoropentylsulfonyl fluoride monomer (ICF 2 CF 2 OCF 2 CF 2 SO 2 F) Reaction for 6h.
[0077] After the mixture was filtered, the mother liquor was rotary evaporated to remove acetonitrile, and the obtained yellow-white solid was recrystallized with deionized water to obtain the product ICF 2 CF 2 OCF 2 CF 2 SO 2 NKSO 2 CF 2 CF 2 OCF 2 COOCH 3 .
[0078] Step 2: Synthesis of fluorine-containing sulfonimide grafted polystyrene with carboxyl groups
[0079] Dissolve 5g of polystyrene with a bromine co...
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