Method of preparing block polyurethane microcapsule composite finishing agent
A technology of polyurethane microcapsules and finishing agents, which can be used in fiber treatment, textiles and papermaking, and can solve the problems of single-function finishing agents
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[0009] The invention provides a method for preparing a block polyurethane microcapsule composite finishing agent, comprising the following steps:
[0010] a) Prepare a block polyurethane prepolymer composed of a soft segment phase and a hard segment phase, and adjust the hard segment content under the condition that the composition and content of the soft segment are fixed, so that the reversible phase is composed of a rich soft segment phase and a short hard segment Phase composition, the stationary phase is composed of a hard segment phase, based on solid content, the mass percentage of the hard segment phase is 20%-50%, and the mass percentage of the soft segment phase is 80%-50%;
[0011] b) Then, the prepared block polyurethane prepolymer and the phase change material are added in a certain ratio to the aqueous solution containing the emulsifier under the condition of rapid stirring, and after emulsification until the particle size of the microcapsule meets the requirement...
Embodiment 1
[0026] The soft segment phase components of the dibutyltin laurate comprising 0.02g, polyethylene glycol (molecular mass 3000, dried), 10g of toluene diisocyanate and 3g of 1,4-butanediol in dry nitrogen protection, 70-80°C reaction temperature, and stirring reaction for 3-4 hours to obtain a polyurethane prepolymer with a soft segment phase structure; then add 14g of 4,4'-diphenylmethane diisocyanate, 2g of 1,4- Butanediol, 3g of carboxyl-containing dimethylolpropionic acid and 1g of crosslinking agent triethanolamine hard segment phase components, at 50 ~ 60 ℃ reaction temperature, stirring continued reaction for about 2 ~ 3 hours, to obtain soft Segment phase and hard segment phase polyurethane prepolymer with block structure.
[0027] Get 55g of block polyurethane prepolymer and 40g of C 12 -C 32 Linear alkanes are added to the aqueous solution containing styrene-maleic anhydride copolymer and T-80 complex emulsifier under heating and rapid stirring to form an oil-in-wat...
Embodiment 2
[0030]Add 0.01g of dibutyltin laurate, 37.99g of polycaprolactone diol (molecular mass 3000), 9g of 2,4-toluene diisocyanate, and 3g of 1,4-butanediol into 500mL of the reversible phase components with a stirrer, In the reaction kettle with a thermometer and a reflux condenser, react at a temperature of 70-80° C. for 3-4 hours. Then lower the temperature to 45-55°C, add 4g of stationary phase components 1,4-butanediol, 3g of trimethylolpropane, 35g of 4,4'-diphenylmethane diisocyanate and 8g of dihydroxybutyric acid, and control the temperature After reacting at 50-60°C for 3-4 hours, a block polyurethane prepolymer composed of a reversible phase and a stationary phase is prepared.
[0031] Get block polyurethane prepolymer 18g and C 12 -C 32 Add 80 g of linear alkanes to the aqueous solution containing styrene-maleic anhydride copolymer and T-60 complex emulsifier under heating and rapid stirring, continue stirring, add 1 g of dimethylol butyric acid and trimethylol Propan...
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