A kind of curing agent for steel bar anticorrosion powder coating
A powder coating and curing agent technology, applied in anti-corrosion coatings, powder coatings, coatings, etc., can solve the problems of low coating flexibility and insufficient reactivity, and achieve the effect of increasing reactivity, flexibility and adhesion
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Embodiment 1
[0011] Preparation of conventional phenolic curing agents
[0012] Using oil heating bulk polymerization method, 100g of epoxy resin E-44 (purchased from Yueyang Petrochemical), 26g of bisphenol A (purchased from Qilu Petrochemical) and 6g of phenolic curing agent CT-3 (purchased from Qilu Petrochemical) Add to the reaction kettle, stir at 180°C for 1-2h, then cool down the whole system to 140°C, then add 26g of bisphenol A and 6g of phenolic curing agent CT-3, and stir at the reaction temperature of 140°C for 1-2h, Prepare conventional phenolic curing agents.
Embodiment 2
[0014] Prepare curing agent of the present invention
[0015] Add the conventional phenolic curing agent prepared in Example 1 and 13.1 g of monovalent polyetheramine M-1000 (purchased from Dalian Liansheng Trading Co., Ltd.) into the reactor, and stir at a reaction temperature of 140° C. for 0.5-1 h. The resulting material is released from the reactor while it is hot, cooled and pulverized to obtain the curing agent of the present invention.
Embodiment 3
[0017] Prepare curing agent of the present invention
[0018] Using oil heating bulk polymerization method, 100g of epoxy resin E-44 (purchased from Yueyang Petrochemical), 30g of bisphenol A (purchased from Qilu Petrochemical) and 8g of phenolic curing agent CT-3 (purchased from Qilu Petrochemical) Add to the reaction kettle, stir at 170°C for 1-2h, then cool down the whole system to 140°C, then add 30g of bisphenol A and 6g of phenolic curing agent CT-3, and stir at the reaction temperature of 140°C for 1-2h, Finally, 8.7g of binary polyetheramine ED-2003 (purchased from Dalian Liansheng Trading Co., Ltd.) was added to the reactor, stirred at a reaction temperature of 140°C for 0.5-1h, and the resulting material was released from the reactor while it was hot, cooled and crushed , to prepare the curing agent of the present invention.
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