反応式
[O-2].[Zn+2:2].[C:3]1([P:9](=[O:12])([OH:11])[OH:10])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>O>[O-2:10].[Zn+2:2].[C:3]1([P:9](=[O:10])([O-:12])[O-:11])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[Zn+2:2]参加物
実験手順
An aqueous slurry of zinc oxide was prepared by charging a 300 mL reaction flask equipped with a stirrer with 10.0 g (123 mmol) of zinc oxide (JIS grade 2, available from HakusuiTech Ltd.) and 90.0 g of water. An aqueous solution of 19.4 g (123 mmol) of phenylphosphonic acid (Nissan Chemical Industries, Ltd.) dissolved in 110.0 g of water was gradually added dropwise at room temperature (about 25° C.) to this slurry with stirring, thereby effecting a reaction for five hours. The slurry was then filtered and the wet cake was thoroughly rinsed with water. The wet cake was subsequently dried at 120° C. for at least 12 hours, yielding a white powder of zinc phenylphosphonate. FIG. 2 shows a micrograph taken with a field-emission scanning electron microscope (SEM: JSM-7400F, manufactured by JEOL Ltd.) of the white powder of zinc phenylphosphonate thus obtained.
後処理
- customa 300 mL reaction flask
- additionwas gradually added dropwise at room temperature (about 25° C.) to this slurry
- customa reaction for five hours
- filtrationThe slurry was then filtered
- washthe wet cake was thoroughly rinsed with water
- customThe wet cake was subsequently dried at 120° C. for at least 12 hours
出典と根拠
- ORDレコード
- ord-417d0d8778664dcdb38fa7a0babaec53
- 出典データセット
- uspto-grants-2015_05
- 特許番号
- US09035100B2
関連ノート
読み込み中…