Polyisocyanate composition having allophanate group and high-solid coating material
A polyisocyanate and allophanate technology, applied in polyurea/polyurethane coatings, coatings, thin material processing, etc., can solve problems such as difficult industrial production
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Embodiment 1
[0174] Embodiment 1 (synthesis example of polyisocyanate composition)
[0175] Polyisocyanate P-1 and polyisocyanate P-2 were mixed at a weight ratio of 30 / 70 to obtain polyisocyanate a-1 of Example 1. NCO% of polyisocyanate a-1 = 18.7% and viscosity = 571 mPa·s. Data such as molecular weight etc. are shown in Table 1.
Embodiment 2-5
[0176] Embodiment 2-5 (synthesis example of polyisocyanate composition)
[0177] Polyisocyanates P-1 to P-5 were mixed to obtain polyisocyanates a-2 to a-6, respectively. The mixing ratio (weight ratio) in each of the obtained polyisocyanates is shown in Table 2. The physical properties of polyisocyanates a-2 to a-6 are shown in Table 1.
Embodiment 7
[0178] Embodiment 7 (synthesis example of polyisocyanate composition)
[0179] 1244 grams of HDI, 16.5 grams of isobutanol, and 38.9 grams of triethylene glycol were charged to the same apparatus as in Monoallophanate Product Synthesis 1. The carbamate forming reaction was carried out at 90° C. for 1 hour with stirring. The temperature was raised to 130° C., and then 0.43 g, 20% solids, of zirconyl 2-ethylhexanoate in mineral spirits was added as an allophanate forming catalyst. After 30 minutes, when the refractive index of the reaction liquid increased by 0.0055, 0.17 grams (2.2 times more than the number of moles of the allophanate-forming catalyst) of 50% solid content of isobutanol solution of pyrophosphoric acid were added thereto to Stop the reaction.
[0180] According to NMR measurements of the reaction liquid, the final molar ratio of allophanate groups to isocyanurate groups was 97:3.
[0181] Then, unreacted HDI was removed under conditions similar to Synthesis ...
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Abstract
Description
Claims
Application Information
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