Boric Acid → Boric Acid
反応式
[O-2].[Ca+2:2].[B:3]([OH:6])([OH:5])[OH:4].[OH:7][Mn:8]=[O:9].[OH:10][Mn:11]=[O:12].[Mn:13]>O>[O-2:4].[Ca+2:2].[B:3]([OH:6])([OH:5])[OH:4].[O-2:7].[Ca+2:2].[B:3]([OH:6])([OH:5])[OH:4].[OH:12][Mn:11]=[O:10].[OH:9][Mn:8]=[O:7].[Mn:13]参加物
反応条件
- 温度
- 600 °C
実験手順
In a similar test evaluation following the procedure described in the example above, calcium oxide based and calcium oxide-boric acid based pigments were prepared and evaluated for inhibitor efficiency. CaO.H3BO3.2Mn3O4 may also be written CaO.1/2B2O3.2Mn3O4 since boric acid is expected to lose a mole of water during the sintering operation. 68.6 Grams of manganomanganic oxide with a mean particle size of 2 microns were mixed with 8.4 grams of calcium oxide with a 2 micron particle size using a high intensity mixer. It was heated in a crucible at 600° C. for 1 hr. and then milled as in Example 1. Similarly a ratio of 1 mol of calcium oxide, 1 mol of boric acid, and 2 mols of manganomanganic oxide were prepared and sintered at 600° C. for 1 hr. 12.4 Grams of micronized boric acid (2 microns), 5.6 grams of calcium oxide and 45.7 grams of Mn3O4 were used during the sintering.
後処理
- customand then milled as in Example 1
出典と根拠
- ORDレコード
- ord-9f41dc23f6824902850b57519c3c4745
- 出典データセット
- uspto-grants-1984_09
- 特許番号
- US04469521
反応ノート
読み込み中…