High solid polyurethane-polyurea dispersoid
A dispersion, water-based polyurethane technology, used in polyurea/polyurethane coatings, devices for coating liquids on surfaces, coatings, etc., can solve the problems of falling solid content, rising viscosity, insufficient performance and stability, etc.
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preparation example Construction
[0061] The preparation of the polyurethane prepolymers can be carried out simultaneously with the partial or complete salt formation of the anionic and / or cationic dispersing groups, or subsequently, if this reaction has not already taken place in the starting molecule. To form anionic groups, bases such as tertiary amines are used. Examples include trialkylamines containing 1 to 12, preferably 1 to 6 carbon atoms in each alkyl group, such as trimethylamine, triethylamine, methyldiethylamine, tripropylamine, N-methylamine morpholine, methyldiisopropylamine, ethyldiisopropylamine and diisopropylethylamine. The alkyl groups may also contain hydroxyl groups, as in the dialkylmonoalkanolamines, alkyldialkanolamines and trialkanolamines. As neutralizing agents, inorganic bases such as ammonia or sodium and / or potassium hydroxide may optionally also be used. Preference is given to triethylamine, triethanolamine, dimethylethanolamine or diisopropylethylamine.
[0062] Based on the...
Embodiment 1
[0096] Example 1 : comparative example, PU dispersion (component I)
[0097] Impranil(R) DLN: an anionic hydrophilic unimodal PU dispersion based on polyester with a solids content of 40% and an average particle size of 100 nm to 300 nm, Bayer AG, Leverkusen, Germany.
Embodiment 2
[0099] 2210.0 g of a difunctional polyester polyol (number average molecular weight 1700 g / mol, OH number 66) prepared from adipic acid, neopentyl glycol and hexanediol was heated to 65°C. Subsequently, a mixture of 195.5 g of hexamethylene diisocyanate and 258.3 g of isophorone diisocyanate was added within 5 minutes at 65° C., and the mixture was stirred at 100° C. until a theoretical NCO content of 3.24% was reached. The finished prepolymer was dissolved in 4800 g of acetone at 50° C. and then a solution of 29.7 g of ethylenediamine, 95.7 g of disulfamic acid salt and 602 g of water was metered in within 5 minutes. This was followed by stirring for 15 minutes. After this, within 20 minutes, 1169 g of water were added for dispersion. The solvent was subsequently removed by vacuum distillation, resulting in a storage-stable bimodal PU dispersion with a solids content of 60%. The solid fraction of the dispersion consisted of 31% fine fraction and 69% coarse fraction. The ma...
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