Waterborne polyurethane printing ink connecting material and preparation method thereof
A technology of ink binder and water-based polyurethane, which can be used in ink, applications, household appliances, etc. It can solve the problems of poor emulsion stability, complicated process, and high cross-linking density, and achieve low surface tension, simple reaction process, and adhesion performance. enhanced effect
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Embodiment 1
[0031] (1) Synthesis of polyurethane prepolymer: Add 60 g of dehydrated polyε-caprolactone diol and 29.8 g of isophorone diisocyanate 80 After keeping the temperature at ℃ for 2 hours, cool down to 75℃ and add 3.98g of dimethylol propionic acid (DMPA) dissolved in 2g of N-methylpyrrolidone, mix and stir for 1.5h, and then slowly dropwise add DMPA mixed with 4g of acetone at 70℃. 4.68g of 1,4-butanediol, dripped in about 15 minutes, kept the temperature for 1.5 hours, and finally lowered the temperature to 50°C and added a small amount of acetone to reduce the viscosity. After 5 minutes, added 3g of triethylamine to neutralize and react for 15 minutes to prepare NCO-terminated polyurethane Polymer.
[0032] (2) Emulsification, post-chain extension and crosslinking of water-based polyurethane prepolymer: cool down the polyurethane prepolymer synthesized in step (1) to about 40°C, pour 120g of deionized water and increase the stirring speed to 6500r / min After the prepolymer was ...
Embodiment 2
[0035](1) Synthesis of polyurethane prepolymer: Add 60 g of dehydrated polyε-caprolactone diol and 36.8 g of isophorone diisocyanate 80 After 2 hours of heat preservation at ℃, cool down to 75℃ and add 2.8g of dimethylol propionic acid (DMPA) dissolved in 1.5g of N-methylpyrrolidone, mix and stir for 1.5h, then slowly add dropwise at 70℃ and mix with 4g of acetone 5.32g of 1,4-butanediol, dripped in about 15min, kept the temperature for 1.5h, and finally cooled to 30-50℃ and added a small amount of acetone to reduce the viscosity. based polyurethane prepolymers.
[0036] (2) Emulsification, post-chain extension and crosslinking of water-based polyurethane prepolymer: cool down the polyurethane prepolymer synthesized in step (1) to about 40°C, pour 140g of deionized water and increase the stirring speed to 6500r / min After the prepolymer was emulsified by phase inversion dispersion for 5 minutes, 2.3g of ethylenediamine was added to extend the chain, and after stirring for 5 mi...
Embodiment 3
[0039] (1) Synthesis of polyurethane prepolymer: Add 60 g of dehydrated polyε-caprolactone diol and 36.8 g of isophorone diisocyanate 80 After keeping the temperature at ℃ for 2 hours, cool down to 75℃ and add 3.8g of dimethylolpropionic acid (DMPA) dissolved in 2g of N-methylpyrrolidone, mix and stir for 1.5h, and then slowly dropwise add DMPA mixed with 4g of acetone at 70℃. 4.62g of 1,4-butanediol, dripped in about 15 minutes, kept the temperature for 1.5 hours, and finally lowered the temperature to about 50°C and added a small amount of acetone to reduce the viscosity. After 5 minutes, added 2.86g of triethylamine to neutralize and react for 15 minutes to obtain NCO-terminated Polyurethane prepolymers.
[0040] (2) Emulsification, post-chain extension and crosslinking of water-based polyurethane prepolymer: cool down the polyurethane prepolymer synthesized in step (1) to about 40°C, pour 140g of deionized water and increase the stirring speed to 6500r / min After the prepo...
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