反応式
N.[CH2:2](O)[CH:3]([OH:5])[CH3:4].CC(C(O)[C:11]([CH2:14][O:15][C:16]([CH:18]([CH3:20])[CH3:19])=[O:17])(C)C)C.N[C:23]([O:25]CC)=[O:24]>C(C(C)=O)C>[CH3:20][C:18]([C:16]([O:15][CH2:14][CH2:11][O:25][C:23]([CH2:2][C:3]([CH3:4])=[O:5])=[O:24])=[O:17])=[CH2:19]参加物
6
実験手順
A 100 g. portion of each polymer was neutralized to pH=9.5 with ammonia, an additional 0.52 g. of ammonia was added (one equivalent based on acetoacetate) to ensure complete enamine formation. To all three samples was added a premix consisting of 0.32 g. nonionic surfactant (Triton X-405; Union Carbide), 4.4 g. propylene glycol, 4.4 g. coalescent (Texanol) and 1.1 g. a 10% aqueous solution of urethane rheology modifier (QR-708; Rohm and Haas). The formulated mixture was equilibrated for 24 hours and then coatings were applied on glass plates to give 3-4 mil thick coatings. Films were placed outdoors in complete sunlight for 12 days. Film swell ratios in methyl ethyl ketone were obtained.
後処理
- additionTo all three samples was added a premix
- customto give 3-4 mil thick coatings
- customfor 12 days
出典と根拠
- ORDレコード
- ord-4ea655d40f514791b9574d2037062719
- 出典データセット
- uspto-grants-1996_10
- 特許番号
- US05562953
関連ノート
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