GB989812A - Production of chlorocyanuric acids - Google Patents
Production of chlorocyanuric acidsInfo
- Publication number
- GB989812A GB989812A GB6858/62A GB685862A GB989812A GB 989812 A GB989812 A GB 989812A GB 6858/62 A GB6858/62 A GB 6858/62A GB 685862 A GB685862 A GB 685862A GB 989812 A GB989812 A GB 989812A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chlorine
- acid
- slurry
- alkaline earth
- cyanurate
- 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
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
A process for.producing a chlorocyanuric acid which comprises introducing chlorine into an aqueous alkaline dispersion of an alkaline earth metal salt of cyanuric acid at a temperature in the range from above the freezing point (-5 DEG C.) of the dispersion, and continuing the addition of chlorine until the pH of the dispersion is reduced to a value below 4. Preferably the temperature is at most 50 DEG C. The alkaline earth cyanurate may be prepared as a 10-30% slurry by mixing a 10-35% aqueous slurry of the alkaline earth carbonate, oxide or hydroxide with a 5-25% slurry of cyanuric acid in stoichiometric proportion, which mixture then has a pH of 12.0-12.6 and to which liquid or gaseous chlorine is added with agitation and external cooling to replace the metal atoms of the cyanurate. The mixture is maintained at 10-35 DEG C. and the chloro cyanuric acid separated, e.g. by centrifuging. The process may be continuous, the chlorine and the slurry of cyanurate being introduced into the reaction zone at 0-50 DEG C. at rates to adjust the pH to below 4 and a portion of the mixture is continuously removed from which the chloro cyanuric acid is separated. Trichlorocyanuric acid is prepared from the trialkaline earth metal dicyanurate using 100-200% of the stoichiometric quantity of chlorine and reducing the pH below 3.5. The dichlorocyanuric acid is prepared from the mono alkaline earth metal monocyanurate using 100-120% of the stoichiometric quantity of chlorine and reducing the pH below 2.5.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US9091261A | 1961-02-23 | 1961-02-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB989812A true GB989812A (en) | 1965-04-22 |
Family
ID=22224926
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB6858/62A Expired GB989812A (en) | 1961-02-23 | 1962-02-22 | Production of chlorocyanuric acids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB989812A (en) |
-
1962
- 1962-02-22 GB GB6858/62A patent/GB989812A/en not_active Expired
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2969360A (en) | Continuous chlorination of cyan uric | |
GB1220963A (en) | Process for the production of phosphoric acid at a high concentration and gypsum by-product of improved quality | |
US2768167A (en) | Cyanuric acid preparation | |
GB989812A (en) | Production of chlorocyanuric acids | |
US2730542A (en) | Process for preparing ethanol-2-aminophosphoric acid | |
US2653971A (en) | Manufacture of anthranilic acid | |
GB519340A (en) | Improved explosive and process of making the same | |
US3404949A (en) | Process for the production of ammonium sulfamate | |
GB825929A (en) | Production of chlorocyanuric acids | |
GB1108926A (en) | Method for producing 5-ª‰-methylmercaptoethylhydantoin | |
US2359319A (en) | Process for the production of ammonium sulphate and elemental sulphur | |
US3270017A (en) | Method for producing stable salts of dichloroisocyanuric acid | |
US3410900A (en) | Production of phenylhydrazine | |
US2938032A (en) | pasotted jx | |
GB1388936A (en) | Chloroisocyanuric acids | |
US1366301A (en) | Process for transforming free or combined ammonia into ammonium sulfate | |
US2259563A (en) | Method of making guanyl urea sulphamate | |
SU138231A1 (en) | Method for producing barium bromate | |
GB923147A (en) | A process for the production of sodium dichloroisocyanurate | |
GB1202426A (en) | Sodium-potassium cyanurates and potassium chloro-cyanurates | |
SU109043A2 (en) | Calcium fluoride production method | |
GB1218209A (en) | A process for the production of aminoguanidine bicarbonate | |
US3074948A (en) | Heterocyclic nitrogen compounds containing sulfonyl fluoride groups and method of producing same | |
GB1066024A (en) | Production of beryllium hydroxide | |
US1910692A (en) | Process for preparing beta-amino-anthraquinones |