Water-based inorganic three-proofing coating and preparation method thereof
An inorganic, water-based technology, applied in anti-corrosion coatings, fire-resistant coatings, anti-fouling/underwater coatings, etc., can solve problems such as fire hazards and air pollution, and achieve the effects of poor water resistance, accelerated curing, and good low-temperature stability
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preparation example 1-3
[0044] Octamethylcyclotetrasiloxane in Preparation Example 1-3 was selected from the octamethylcyclotetrasiloxane of model D3 sold by Shandong Xinjie Environmental Protection Technology Co., Ltd., and the phenalkamine curing agent in Preparation Example 1-3 was selected from Shandong Deyuan Epoxy Technology Co., Ltd. DFT-31, γ-glycidyl ether oxypropyl trimethoxysilane was selected from the γ-glycidyl ether oxypropyl silane model AC-66 sold by Fangzhou (Fogang) Chemical Materials Co., Ltd. trimethoxysilane.
preparation example 1
[0045] Preparation Example 1: (1) According to the raw material ratio in Table 1, 10kg octamethylcyclotetrasiloxane and 5kg γ-glycidyl ether oxypropyltrimethoxysilane were mixed uniformly;
[0046] (2) 8kg of emulsifier, 15kg of deionized water, 3kg of sodium hydroxide and 1kg of phenalkamine curing agent are heated to 65°C at a rotational speed of 400r / min, the product of step (1) is added within 1.5h, and the reaction is kept for 9h , sharply cooled to 30°C, neutralized with acetic acid, filtered, and discharged to obtain an anionic silicone emulsion. The emulsifier includes polyoxyethylene octylphenol ether, sodium lignosulfonate and Dodecylbenzenesulfonic acid.
[0047] The raw material ratio of the anionic silicone emulsion in the preparation example 1-3 of table 1
[0048]
preparation example 2
[0049] Preparation Example 2: (1) According to the raw material ratio in Table 1, 15kg octamethylcyclotetrasiloxane and 8kg γ-glycidyl ether oxypropyltrimethoxysilane were mixed uniformly;
[0050] (2) 9kg of emulsifier, 25kg of deionized water, 4kg of sodium hydroxide and 2kg of phenalkamine curing agent were heated to 68°C at a rotating speed of 500r / min, and the product of step (1) was added within 1.3h, and the reaction was incubated for 9h. , sharply cooled to 35°C, neutralized with acetic acid, filtered and discharged to obtain an anionic silicone emulsion. The emulsifier includes polyoxyethylene octylphenol ether, sodium lignosulfonate and Dodecylbenzenesulfonic acid.
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