GB611439A - Improvements in or relating to the production of alkali metal perborate compositions - Google Patents
Improvements in or relating to the production of alkali metal perborate compositionsInfo
- Publication number
- GB611439A GB611439A GB12831/46A GB1283146A GB611439A GB 611439 A GB611439 A GB 611439A GB 12831/46 A GB12831/46 A GB 12831/46A GB 1283146 A GB1283146 A GB 1283146A GB 611439 A GB611439 A GB 611439A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkali metal
- mol
- boric acid
- peroxide
- solution
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B15/00—Peroxides; Peroxyhydrates; Peroxyacids or salts thereof; Superoxides; Ozonides
- C01B15/055—Peroxyhydrates; Peroxyacids or salts thereof
- C01B15/12—Peroxyhydrates; Peroxyacids or salts thereof containing boron
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
Alkali metal perborate compositions are prepared by mixing boric acid (i.e. boric oxide, ortho- or pyro-boric acid) or an alkali metal borate, e.g. borax, with hydrogen peroxide, an alkali metal peroxide or hydroxide and sufficient water to cause reaction between the boron compound and the peroxide and to form a substantially homogeneous solution, and rapidly dehydrating the solution until a homogeneous solid product is obtained. The dehydration, the temperature of which is not lower than 100 DEG C. and preferably is between 100 DEG and 150 DEG C., may be continued until the residual water content of the product is not more than 5 per cent in excess of that required to be equivalent to the H2O2 content as calculated from the active oxygen content. The proportion employed may be from 0.2 to 0.96 mol. and preferably from about 0.8 to 0.96 mol. of Na2O2 for each mol. of Na2B4O7. Other salts of boric acid, i.e. metaborates or tetraborates, may be used instead of borax. The stability in storage and in solution may be increased by addition of sodium pyrophosphate or of sodium silicate and magnesium sulphate.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US611439XA | 1945-04-28 | 1945-04-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB611439A true GB611439A (en) | 1948-10-29 |
Family
ID=22033895
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12831/46A Expired GB611439A (en) | 1945-04-28 | 1946-04-29 | Improvements in or relating to the production of alkali metal perborate compositions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB611439A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2947602A (en) * | 1955-08-29 | 1960-08-02 | Shell Oil Co | Production of sodium perborate in stable form |
-
1946
- 1946-04-29 GB GB12831/46A patent/GB611439A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2947602A (en) * | 1955-08-29 | 1960-08-02 | Shell Oil Co | Production of sodium perborate in stable form |
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