Process for making urethane-isocyanurates
A technology of isocyanurate and polyisocyanurate, applied in the field of polyisocyanurate and polyurethane-isocyanurate polymers, can solve the problems of loss of resin characteristics, loss of quality, etc.
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[0043] The following examples are provided to illustrate exemplary embodiments and are not intended to limit the scope of the invention. All parts and percentages are by weight unless otherwise stated.
[0044] The following materials are mainly used in the mixture:
[0045]
[0046] Polyisocyanurates or polyurethane-isocyanurate polymers are prepared by the following general methods:
[0047] For stage (a), the polyol (shown in Tables 1 and 2 below) was charged into the mixing chamber of a high speed laboratory mixer (FlackTek SpeedMixer). The corresponding catalysts according to Tables 1 and 2 below were then added to the polyol and mixed thoroughly at 800 rpm for 5 seconds followed by 2000 rpm for 10 seconds. The corresponding polyisocyanates according to Tables 1 and 2 below were then added to the mixing chamber and mixed with the other components under the same mixing conditions. The resulting reaction mixture was emptied onto a circular steel mold with a diameter...
example 4 and example 5
[0058] For Examples 4 and 5, the polyol (Polyol E) was a trifunctional polyether polyol having predominantly primary hydroxyl end groups. For Examples 6 and 7, the polyol was a filled polyol. T of the post-cured samples in Examples 4 to 7 g is 160°C or higher, and its modulus at 121°C is higher than 7×10 8 Pa. After humidity aging, the T of each of Examples 4 to 7 g raised. This value is much higher than Comparative Examples A, B and C. The corrected 121°C G' also increased after humidity aging, as opposed to Comparative Examples A, B and C.
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