Humectant and dispersant, production and use thereof
A technology of reaction and addition compounds, which is applied in the field of preparation of these addition compounds, can solve the problems of inability to use, poor compatibility of dispersants, and inability to fully ensure the sufficient stabilization of granular solids to be dispersed, and achieve the effect of broad usefulness
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[0171] For substances that do not have molecular homogeneity, the stated molecular weights—hereafter as already described above—denote the mean value of the values. In the presence of titratable hydroxyl or amino groups, molecular weight or number-average molecular weight M n . For compounds for which end group determination cannot be applied, the number average molecular weight is determined by gel permeation chromatography based on polystyrene standards.
[0172] Parts are parts by weight and percentages are percent by weight unless otherwise indicated.
[0173] According to EN ISO 9369, the free NCO content of the polyisocyanate used and the course of the NCO addition reaction were determined by reaction with butylamine and subsequent titration of excess amine. These methods are also described in "The Chemistry of Cyanates and their ThioDerivatives" by Saul Patai, Part 1, Chapter 5, 1977.
[0174] Hydroxy-functional caprolactone polyesters are prepared as described, for ...
Embodiment 1
[0176] Embodiment 1 (non-invention, comparative example)
[0177] 28.1 parts of polyisocyanate P1 were homogenized with 38.5 parts of BCPE1100 and 22.7 parts of PMA (methoxypropyl acetate). The mixture was heated to 80° C. under an inert gas, and 0.003 parts of DBTL (dibutyltin dilaurate) were added. The mixture was stirred at this temperature for about 1 hour until 65% of the NCO groups used had reacted. Then 2 parts of DMAPA were added and stirring was continued at 80 °C until all NCO groups were consumed by reaction. The product was of medium viscosity with a solids content of 60% and an amine value of 12 mg KOH / g. After several days at 20°C, the product showed a strong formation of crystals.
[0178] The product is insoluble in aromatic-free petroleum solvents.
Embodiment 2
[0180]Similar to Example 1, 38.5 parts of BPO1100 was used instead of BCPE1100. The solids content was 60% and the amine number was 12 mg KOH / g. On storage, the product remained homogeneous and liquid. No crystals are formed even during long-term storage below 0°C.
[0181] A clear 10% solution can be prepared in aromatic-free white spirit.
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