UV adhesive and its application
A viscose and multi-functionality technology, applied in the direction of adhesives, polyurea/polyurethane adhesives, adhesive types, etc., can solve the problems of inability to adjust the initial adhesion, inconvenient, and not environmentally friendly
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Examples
Embodiment 1
[0044]Synthesis of cured resin: React 1.2mol hydroxyethyl methacrylate, 0.7mol IPDI and 0.3mol polyethylene adipate (molecular weight: 5000) at 60-80°C for 1-3 hours to obtain cured resin A 1 .
[0045] A component: curing resin A 1 10 g, 40 g of trimethylolpropane triacrylate, 20 g of aliphatic urethane acrylate oligomer-Sartomer CN8011 (functionality 6), 6 g of α-hydroxy ketone.
[0046] Component B: 50 g Bayer HDI aliphatic isocyanate 7790 (NCO content 17%).
[0047] Production method: Put the cured resin and active monomer raw materials into the mixing tank in turn and stir for half an hour, filter to obtain component A, and then put them into different containers with component B to obtain the final product.
Embodiment 2
[0049] Synthesis of cured resin: React 0.3mol hydroxyethyl acrylate, 0.5mol IPDI and 0.8mol polyethylene glycol (molecular weight 200) at 60-80°C for 1-3 hours to obtain cured resin A 2 .
[0050] A component: curing resin A 2 40 g, 20 g of pentaerythritol tetraacrylate, 30 g of aliphatic urethane acrylate oligomer-Sartomer CN8011 (functionality: 6), 5 g of α-hydroxyketone, and 5 g of acylphosphine oxide.
[0051] Component B: 99 grams of BASF HB175 (NCO content 16.5%), 0.5 grams of defoamer Tego Airex910, 0.5 grams of leveling agent BYK333.
[0052] Production method: Curing resin A 2 Put it into the mixing tank with active monomer raw materials and stir for half an hour, filter to obtain component A, and then put it into different containers with component B to obtain the final product.
Embodiment 3
[0054] Synthesis of cured resin: react 1.2mol hydroxyethyl acrylate, 1.0mol IPDI and 1.0mol pentanediol at 60-80°C for 1-3 hours to obtain cured resin A 3 .
[0055] A component: curing resin A 3 20g, dipentaerythritol hexaacrylate 30g, aliphatic urethane acrylate oligomer-Sartomer CN8011 (functionality 6) 10g, 2,4,6-(trimethylbenzoyl) diphenylphosphine oxide 1g .
[0056] Component B: 60 g of Bayer HDI aliphatic isocyanate 7790 (NCO content 17%).
[0057] Production method: Curing resin A 3 Put them into the mixing tank with the active monomer raw materials in sequence for half an hour at medium speed, filter to obtain component A, and then put them into different containers with component B to obtain the final product.
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Abstract
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