Plastic bottom coating agent with inorganic film, plastic with inorganic film and decorative film formed by in-mold molding or insert molding
A technology of inorganic thin film and primer, applied in the direction of coating, synthetic resin layered products, polyurea/polyurethane coating, etc., can solve the problems of whitening parts, damage to the aesthetics of plastic technical performance of inorganic thin film, interference fringes, etc. , to achieve the effect of good adhesion
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manufacture example 1
[0048] Add 36 parts (about 0.36 moles) of methyl methacrylate and 111.6 parts (about 0.36 moles) of butyl methacrylate (about 0.78 mol) (about 82.1 mol% in the total of (a1) component and (a2) component) and 32.4 parts (about 0.25 mol) of 2-hydroxyethyl methacrylate (about 0.25 mol) (in (a1) component and (a2) component 17.9 mol% in the total) and 270 parts of methyl ethyl ketone, and the reaction system was set at 80°C. Next, 0.9 parts of azobisisobutyronitrile was added, and the mixture was kept at around 80° C. for 5 hours. Next, 1.8 parts of azobisisobutyronitrile was added, and the reaction system was further kept at around the same temperature for 3 hours. Thereafter, the solution of the target copolymer (A-1) (hereinafter referred to as (A-1) component) was obtained by cooling the reaction system to room temperature. Table 1 shows the raw material type, hydroxyl group concentration, carboxyl group concentration, glass transition temperature and weight average molecula...
manufacture example 2~25, comparative manufacture example 1~3
[0050] The kind and usage amount (mol %) of the monomers used were replaced as shown in Table 1, except that, it was carried out in the same manner as in Production Example 1, and copolymers (A-2) to (A-25 ) and comparative copolymers (□) and (□). Table 1 shows their hydroxyl concentration, carboxyl concentration, glass transition temperature, and weight average molecular weight. In addition, since the solution of copolymer (H) was cloudy white, the subsequent evaluation was not performed.
[0051] 【Table 1】
[0052]
[0053] 【Table 2】
[0054]
[0055] In Tables 1 and 2, the meanings of the symbols are as follows.
[0056] MMA: methyl methacrylate
[0057] BMA: n-butyl methacrylate
[0058] nBA: n-butyl acrylate
[0059] St: Styrene
[0060] 2HEMA: 2-Hydroxyethyl methacrylate
[0061] 2HEA: 2-Hydroxyethyl Acrylate
[0062] 4HBA: 4-Hydroxybutyl Acrylate
[0063] CHDMMA: 4-(hydroxymethyl)cyclohexylmethyl 2-hydroxypropionate
[0064] HEAA: N-(2-Hydroxyethyl)acryla...
manufacture example 26
[0074] In the same reaction vessel as that of Production Example 1, add the isocyanuric polymer of toluene diisocyanate (product name "Coronate2030", the concentration of isocyanate group is 3.8×10 -3 mol / g) 445.5 parts, 5.0 parts of 1,6-hexanediol, and 55.6 parts of methyl ethyl ketone were subjected to urethanization reaction at 60° C. for 3 hours. Thereafter, it was cooled to room temperature to obtain a modified toluene diisocyanate isocyanuric polymer (hereinafter referred to as "modified TDI-1". The isocyanate group concentration was 1.5×10 -3 mol / g).
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