GB825929A - Production of chlorocyanuric acids - Google Patents

Production of chlorocyanuric acids

Info

Publication number
GB825929A
GB825929A GB3369755A GB3369755A GB825929A GB 825929 A GB825929 A GB 825929A GB 3369755 A GB3369755 A GB 3369755A GB 3369755 A GB3369755 A GB 3369755A GB 825929 A GB825929 A GB 825929A
Authority
GB
United Kingdom
Prior art keywords
tri
reaction
solution
cyanurate
less
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
Application number
GB3369755A
Inventor
William Lewis Robinson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Monsanto Chemicals Ltd
Monsanto Chemical Co
Original Assignee
Monsanto Chemicals Ltd
Monsanto Chemical Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Monsanto Chemicals Ltd, Monsanto Chemical Co filed Critical Monsanto Chemicals Ltd
Priority to GB3369755A priority Critical patent/GB825929A/en
Publication of GB825929A publication Critical patent/GB825929A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12Heterocyclic 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
    • C07D251/26Heterocyclic 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
    • C07D251/30Only oxygen atoms
    • C07D251/36Only oxygen atoms having halogen atoms directly attached to ring nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12Heterocyclic 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
    • C07D251/26Heterocyclic 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
    • C07D251/28Only halogen atoms, e.g. cyanuric chloride

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Di- and/or tri-chlorocyanuric acid is produced by intimately admixing an aqueous solution of di-alkali metal cyanurate and/or tri-sodium cyanurate and at least the stoichiometric proportion of gaseous chlorine in an aqueous reaction medium at a temperature not exceeding 25 DEG C., the conditions of mixing being such that the pH is maintained below 4.5, preferably 3-4.5. The di- and/or tri-chlorocyanuric acid is isolated from the reaction mixture in commercial operation after a residence time in the reaction zone sufficiently limited to produce a yield of at least 75%, preferably 85% to prevent appreciable decomposition. In the production of tri-chlorocyanuric acid the pH of the reaction mixture is more preferably 3-4.3. It is preferred to employ a 5-20%, more preferably a 10-15%, stoichiometric excess of chlorine. Alkali metals specified are sodium and potassium. The reaction temperature is preferably 10-25 DEG C. (which temperature is preferably maintained by cooling the cyanurate solution to -5 DEG to 10 DEG C.), but temperatures as low as -9 DEG C. may be employed. A continuous process in which the reaction product is periodically or continuously removed from the reaction zone is preferably employed, and the volume of solution in the reaction zone is preferably maintained substantially constant. The solid chlorocyanuric acid produced may be removed from solution by filtration, decantation or centrifugation with less than 40%, preferably with less than 15% of water, and dried to a water content of less than 4%, preferably below 1.5%. Specification 634,801 is referred to.
GB3369755A 1955-11-24 1955-11-24 Production of chlorocyanuric acids Expired GB825929A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3369755A GB825929A (en) 1955-11-24 1955-11-24 Production of chlorocyanuric acids

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3369755A GB825929A (en) 1955-11-24 1955-11-24 Production of chlorocyanuric acids

Publications (1)

Publication Number Publication Date
GB825929A true GB825929A (en) 1959-12-23

Family

ID=10356283

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3369755A Expired GB825929A (en) 1955-11-24 1955-11-24 Production of chlorocyanuric acids

Country Status (1)

Country Link
GB (1) GB825929A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1110165B (en) * 1960-01-26 1961-07-06 Basf Ag Process for the preparation of dichloroisocyanuric acid and mixtures containing same
FR2402650A1 (en) * 1977-09-08 1979-04-06 Chlor Chem Ltd CONTINUOUS PROCESS FOR THE PRODUCTION OF DI- OR TRICHLOROCYANURIC ACID BY CHLORINATION OF SODIUM CYANURATE

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1110165B (en) * 1960-01-26 1961-07-06 Basf Ag Process for the preparation of dichloroisocyanuric acid and mixtures containing same
FR2402650A1 (en) * 1977-09-08 1979-04-06 Chlor Chem Ltd CONTINUOUS PROCESS FOR THE PRODUCTION OF DI- OR TRICHLOROCYANURIC ACID BY CHLORINATION OF SODIUM CYANURATE

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