反応式
[OH-].[Zr+4:2].[OH-].[OH-].[OH-].[Zr].[P:7](=[O:11])([OH:10])([OH:9])[OH:8].[P]>O>[P:7]([O-:11])([O-:10])([O-:9])=[O:8].[Zr+4:2].[P:7]([O-:11])([O-:10])([O-:9])=[O:8].[P:7]([O-:11])([O-:10])([O-:9])=[O:8].[P:7]([O-:11])([O-:10])([O-:9])=[O:8].[Zr+4:2].[Zr+4:2]参加物
6
反応条件
- 温度
- 80 °C
実験手順
Catalyst preparation. A zirconium phosphate based catalyst was prepared by a co-precipitation method. A solution of zirconium hydroxide (Zr(OH)4) as a zirconium precursor was dissolved in deionized water. To this solution, a stoichiometric amount of phosphoric acid as a phosphorus precursor was added. The resulting mixture was heated at 80° C. for 2 hours to remove water, and a paste was obtained. The resulting paste was then dried in an oven at 100° C. overnight (about 12-18 hours) to remove the bulk of any remaining water, and to provide a powder. The powder was then calcined at 350° C. for 2 hours to obtain powdered zirconium phosphate.
後処理
- customCatalyst preparation
- customA zirconium phosphate based catalyst was prepared by a co-precipitation method
- customto remove water
- customa paste was obtained
- customThe resulting paste was then dried in an oven at 100° C. overnight (about 12-18 hours)
- customto remove the bulk of any remaining water
- customto provide a powder
出典と根拠
- ORDレコード
- ord-5158bc0245e144c6ba10bfddbe185877
- 出典データセット
- uspto-grants-2014_06
- 特許番号
- US08741258B2
関連ノート
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