Method for preparing non-ionic hyperbranched linear polymer emulsifier
A technology of hyperbranched polymers and linear polymers, applied in chemical instruments and methods, chemical/physical processes, transportation and packaging, etc., can solve problems such as insufficient penetration, poor fluidity, high viscosity, etc., to achieve The effect of stability
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example 1
[0013] First, 1 mol of diethanolamine was dissolved in a certain amount of methanol, 2 mol of methyl acrylate was added dropwise, stirred at 35° C. for 4 hours, and vacuum filtered at 0.08 MPa for 1 hour to obtain monomers for preparing hyperbranched polymers.
[0014] Stir and mix trimethylolpropane and p-toluenesulfonic acid at 115°C, then add the monomer dropwise to trimethylolpropane at a molar ratio of 6:1 between the above monomer and trimethylolpropane, at 100°C The mixture was stirred and reacted for 1 hour, then transferred to a rotary evaporator at 120° C. and 0.01 MPa pressure for 3 hours to obtain a hydroxyl-terminated hyperbranched polymer, wherein the mass fraction of p-toluenesulfonic acid was 2% of the total mass;
[0015] The hydroxyl-terminated hyperbranched polymer and oleic acid were mixed in a molar ratio of 3:1, and rotated at 100°C for 3 hours at a pressure of 0.01MPa. A nonionic hyperbranched-linear polymer emulsifier is obtained.
example 2
[0017] Dissolve 1 mol of diethanolamine in a certain amount of methanol, dropwise add 3 mol of methyl acrylate, stir and react at 15°C for 6 hours, and vacuumize for 1 hour under a pressure of 0.5 MPa to obtain monomers for preparing hyperbranched polymers,
[0018] Stir and mix trimethylolpropane and p-toluenesulfonic acid at 115°C, then add the monomer dropwise to trimethylolpropane at a ratio of 4:1 molar ratio of the above monomers to trimethylolpropane, at 110°C The mixture was stirred and reacted for 1.5 hours, then transferred to a rotary evaporator at 130°C and 0.1MPa pressure for 1.5 hours to obtain a hydroxyl-terminated hyperbranched polymer, wherein the mass fraction of p-toluenesulfonic acid was 0.5% of the total mass;
[0019] The hyperbranched polymer and stearic acid were rotated at 140°C and 0.05MPa for 5 hours at a ratio of 2:1 to obtain a nonionic hyperbranched-linear polymer emulsifier.
example 3
[0021] Dissolve diethanolamine in a certain amount of methanol, add methyl acrylate dropwise to the methanol solution of diethanolamine according to the ratio of methyl acrylate to diethanolamine molar ratio of 2:1, stir at 35°C for 4 hours, and the pressure is 0.1MPa Vacuum under the pressure of 1 hour to obtain the monomer for preparing hyperbranched polymer.
[0022] Stir and mix trimethylolpropane and dry hydrochloric acid at 115°C, then add monomers dropwise to trimethylolpropane at a ratio of 3:1 molar ratio of the above monomers to trimethylolpropane, at 130°C Stirring and reacting for 1.5 hours, transferred to a rotary evaporator at 150°C and 0.5MPa pressure for 3 hours to obtain a hydroxyl-terminated hyperbranched polymer, wherein the mass fraction of p-toluenesulfonic acid was 4% of the total mass;
[0023] Add palmitoyl chloride into the flask according to the molar ratio of hydroxyl-terminated hyperbranched polymer to palmitoyl chloride at a ratio of 5:1, and rotat...
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