Isocyanate composition containing a masked and an unmasked isocyanate and their use for coating
A technology of isocyanate and free isocyanate, which is applied in the field of isocyanate composition and can solve problems such as toxicity
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Embodiment 1
[0067] Synthesis example of powder with free NCO IPDT. Example 1-Powder polyisocyanate composition (triazole blocked HDT / IPDT (70 / 30 weight / Weight)
[0068] 290g of hexamethylene diisocyanate trimer (Tolonate HDT) (NCO content: 0.521 equivalent / 100g), 107.5g of 1,2,4-triazole and 3.98g of triethylamine (relative to all compounds, 1% ( Mass) / 2.6 mol% relative to the free NCO functional groups of HDT) were added sequentially to the stirred, jacketed reactor. The reaction medium is heated to 95°C. The reaction is exothermic and the temperature of the reaction medium rises to 125°C. The temperature slowly dropped back to 95°C. After 1 hour and 30 minutes, infrared analysis of the sample showed that all isocyanate functional groups were blocked by triazole. Then, 170.5 g of isophorone diisocyanate trimer (IPDT) (NCO content: 0.45 equivalent / 100 g) was added at 110°C. After mixing for 15 minutes, the product was decanted and then ground to obtain 568 g of a white powder with a stora...
Embodiment 2
[0070] Example 2-Synthesis of powder polyisocyanate composition (triazole / p-hydroxybenzyl Acid (80 / 20mol / mol) blocked HDT / IPDT (70 / 30 weight / weight)). (TOL 6598)
[0071] 201.84g Tolonate HDT, 58.11g 1,2,4-triazole and 33.41g p-hydroxybenzoic acid were sequentially added to a stirred 500ml jacketed reactor. The reaction mixture was heated to 90°C. After reacting for 1 hour, 2.93 g of triethylamine was added. After 1 hour and 30 minutes, infrared analysis of the sample showed that all isocyanate functional groups were blocked by triazole. 125.73 g of isophorone diisocyanate trimer was added at 110°C. After 1 hour of mixing, the product was decanted and then ground to obtain 420 g of a white powder with storage stability and a Tg of 45°C (that is, 20°C higher than the product without IPDT).
[0072] The composition therefore includes HDT polyisocyanates having isocyanate functional groups masked by a mixture of blocking agents, one of which includes carboxylic acid functional gr...
Embodiment 3
[0075] Example 3 (comparative)-HDT masked by triazole
[0076] Add the following components to a 250ml reactor in turn-107.5g hexamethylene diisocyanate isocyanurate trimer known to the public under the trade name HDT. Its isocyanate (NCO) functional group content is 0.526mol NCO Functional group / 100g product, -39.3g 1,2,4-triazole (purity equal to 99.5%).
[0077] The reaction mixture was then heated to 130°C and stirred. After 1 hour of reaction, infrared analysis of the reaction mass sample showed that the reaction to mask the isocyanate functional group was terminated. Observed at 2272cm -1 The band representing the isocyanate functional group disappeared.
[0078] The product was then poured on the plate and then allowed to cool. The product is then milled at a temperature of -10°C.
[0079] At room temperature, the ground product behaves similarly to the immediately used binder (sticky as bitumen) and cannot be obtained as a powder for disposal under ordinary industrial con...
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