Malonic ester blocked HDI trimer with IPDA stabilization and formaldehyde stabilization
A polyisocyanate and formaldehyde technology, applied in the use of 1-amino-3, can solve the problems of insufficient prevention of turbidity and precipitation, and achieve the effects of less thermal yellowing, reduced thermal yellowing, and good coating performance.
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Embodiment 1
[0043] Embodiment 1 (according to the present invention)
[0044] The blocked polyisocyanate crosslinker described herein has an IPDA content of 2.32 wt% and a formaldehyde content of 2.46 wt%, on a solids basis.
[0045] Element
[0046] 196.0g based on having an NCO content of 21.4wt%, at
[0047] Viscosity at 23°C is about 3000mPas
[0048] The content of 1,6-diisocyanatohexane (HDI)
[0049] Isocyanurate Coating Polyisocyanate
[0050] 152.0g (0.95mol) diethyl malonate
[0051] 3.0g 30% solution of sodium methoxide in methanol
[0052] 8.5g 3,3,5-trimethyl-5-aminomethylcyclohexylamine
[0053] (IPDA)
[0054] 9.0g (0.30mol) paraformaldehyde
[0055] 0.9g 30% solution of sodium methoxide in methanol
[0056] 40.6g N-methylpyrrolidone (NMP)
[0057] 40.6g isobutanol (IB)
[0058] 40.6g butyl glycol (BG)
[0059] 4.8g dibutyl phosphate
[0060] 496.0g
[0061] ...
Embodiment 2
[0068] Embodiment 2 (comparative example)
[0069] The crosslinker was again prepared as in Example 1 with the following changes: 8.5 g of IPDA was omitted and 16.0 g of diethyl malonate was used instead. The crosslinker became cloudy after 7 days of storage at room temperature, but remained liquid.
Embodiment 3
[0070] Embodiment 3 (comparative example)
[0071] The crosslinker was again prepared as in Example 2 with the following changes: No formaldehyde was introduced. Compared to the crosslinker of Example 1, IPDA and formaldehyde are therefore absent.
[0072] After 3 days of storage at room temperature, the crosslinker cured to a glass-like, transparent composition.
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