Solvent-free quick-drying ultra-high solid content methyl methacrylate coating resin and its synthesis method
A technology of methyl methacrylate and isooctyl methacrylate, which is applied in the field of solvent-free fast-drying ultra-high solid content methyl methacrylate coating resin and its synthesis, can solve the problem of no obvious increase in polymer solid content, Problems such as large energy loss and increased cost can achieve the effects of high appearance flatness, extended storage period, and improved prepolymerization rate
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Embodiment 1
[0069] The medicine and dosage used in the present embodiment are as follows:
[0070] 45 parts of methyl methacrylate;
[0071] 15 parts of isooctyl methacrylate;
[0072] 7 parts of lauryl methacrylate;
[0073] 2 parts of N,N diethyl-p-toluidine;
[0074] 4 parts of benzoyl peroxide;
[0075] 0.00015 parts of hydroquinone;
[0076] Azobisisobutyronitrile 0.9 parts.
[0077] The specific polymerization process is as follows:
[0078] 1.45 parts of methyl methacrylate, 4 parts of dodecyl methacrylate, plus 0.6 parts of azobisisobutyronitrile, pre-polymerized at 40°C, reacted for 30 minutes, and the viscosity of the system after the reaction was 0.0093Pa .s. This step realizes the pre-polymerization of methyl methacrylate and dodecyl methacrylate.
[0079] 2.15 parts of isooctyl methacrylate, 3 parts of dodecyl methacrylate, plus 0.3 parts of azobisisobutyronitrile, pre-polymerized at a temperature of 35 ° C, reacted for 30 minutes, and the viscosity of the system afte...
Embodiment 2
[0086] The medicine and dosage used in the present embodiment are as follows:
[0087] 45 parts of methyl methacrylate;
[0088] 15 parts of isooctyl methacrylate;
[0089] 7 parts of lauryl methacrylate;
[0090] 2 parts of N,N diethyl-p-toluidine;
[0091] 4 parts of benzoyl peroxide;
[0092] Azobisisobutyronitrile 0.9 parts.
[0093] The specific polymerization process is as follows:
[0094] 1.45 parts of methyl methacrylate, 4 parts of dodecyl methacrylate, plus 0.6 parts of azobisisobutyronitrile, pre-polymerized at 40°C, reacted for 30 minutes, and the viscosity of the system after the reaction was 0.0095Pa .s. This step realizes the pre-polymerization of methyl methacrylate and dodecyl methacrylate.
[0095] 2.15 parts of isooctyl methacrylate, 3 parts of dodecyl methacrylate, plus 0.3 parts of azobisisobutyronitrile, pre-polymerized at a temperature of 35 ° C, reacted for 30 minutes, and the viscosity of the system after the reaction was 0.0082 Pa.s. Realize...
Embodiment 3
[0102] The medicine and dosage used in the present embodiment are as follows:
[0103] 45 parts of methyl methacrylate;
[0104] 15 parts of isooctyl methacrylate;
[0105] 7 parts of lauryl methacrylate;
[0106] 2 parts of N,N diethyl-p-toluidine;
[0107] 4 parts of benzoyl peroxide;
[0108] 0.00015 parts of hydroquinone;
[0109] Azobisisobutyronitrile 0.9 parts.
[0110] The specific polymerization process is as follows:
[0111] 1.45 parts of methyl methacrylate, 4 parts of dodecyl methacrylate, plus 0.6 parts of azobisisobutyronitrile, pre-polymerized at 40°C, reacted for 30 minutes, and the viscosity of the system after the reaction was 0.0096Pa .s. This step realizes the pre-polymerization of methyl methacrylate and dodecyl methacrylate.
[0112] 2.15 parts of isooctyl methacrylate, 3 parts of dodecyl methacrylate, plus 0.3 parts of azobisisobutyronitrile, pre-polymerized at a temperature of 35 ° C, reacted for 30 minutes, and the viscosity of the system afte...
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