GB887874A - Purification process for isocyanates - Google Patents

Purification process for isocyanates

Info

Publication number
GB887874A
GB887874A GB20172/59A GB2017259A GB887874A GB 887874 A GB887874 A GB 887874A GB 20172/59 A GB20172/59 A GB 20172/59A GB 2017259 A GB2017259 A GB 2017259A GB 887874 A GB887874 A GB 887874A
Authority
GB
United Kingdom
Prior art keywords
petroleum
isocyanate
isocyanates
employed
solvent
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
GB20172/59A
Inventor
Tadeusz Antoni Kantyka
Clifford Toyne
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB20172/59A priority Critical patent/GB887874A/en
Publication of GB887874A publication Critical patent/GB887874A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C265/00Derivatives of isocyanic acid
    • C07C265/14Derivatives of isocyanic acid containing at least two isocyanate groups bound to the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C263/00Preparation of derivatives of isocyanic acid
    • C07C263/10Preparation of derivatives of isocyanic acid by reaction of amines with carbonyl halides, e.g. with phosgene
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C263/00Preparation of derivatives of isocyanic acid
    • C07C263/18Separation; Purification; Stabilisation; Use of additives
    • C07C263/20Separation; Purification

Landscapes

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

Abstract

A process for eliminating impurities from crude organic isocyanates obtained by phosgenating primary amines in the presence of inert solvents comprises mixing the crude organic isocyanate and the inert solvent in which it is dissolved with a petroleum fraction as defined below, mechanically removing impurities thereby precipitated, and distilling the mixture to recover the organic isocyanate, inert solvent and petroleum fraction. The petroleum fraction employed is any liquid hydrocarbon fraction obtained during the distillation or cracking of crude petroleum which contains a substantial proportion of paraffinic hydrocarbons and has a boiling range the upper limit of which is below the boiling point of the isocyanate and which is sufficiently different from that of the inert solvent to facilitate separation by fractional distillation, e.g. petroleum ether or kerosene. The process may be employed for purifying mono-, di- and tri-isocyanates, especially aromatic isocyanates, e.g. tolylene- and diphenylmethane diisocyanate. The solvent in the phosgenation reaction may be any solvent capable of dissolving the amine employed as starting material and the isocyanate produced, e.g. chlorinated aromatic hydrocarbons such as o-dichlorobenzene. The phosgenation reaction mixture may be concentrated before addition of the petroleum fraction. The impurities may be removed by filtration or centrifuging. In examples an o-dichlorobenzene solution of tolylene diisocyanate, obtained by phosgenating tolylene diamine is mixed with petroleum spirit boiling at 115 DEG C.-125 DEG C., the residue is filtered off and the desired isocyanate recovered from the filtrate by fractionation.
GB20172/59A 1959-06-12 1959-06-12 Purification process for isocyanates Expired GB887874A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB20172/59A GB887874A (en) 1959-06-12 1959-06-12 Purification process for isocyanates

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB20172/59A GB887874A (en) 1959-06-12 1959-06-12 Purification process for isocyanates

Publications (1)

Publication Number Publication Date
GB887874A true GB887874A (en) 1962-01-24

Family

ID=10141577

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20172/59A Expired GB887874A (en) 1959-06-12 1959-06-12 Purification process for isocyanates

Country Status (1)

Country Link
GB (1) GB887874A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3211631A (en) * 1965-10-12 Noilvttitsig gnv noijovhlxh
EP0133538A2 (en) * 1983-08-11 1985-02-27 Bayer Ag Process for the purification of polyisocyanates

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3211631A (en) * 1965-10-12 Noilvttitsig gnv noijovhlxh
EP0133538A2 (en) * 1983-08-11 1985-02-27 Bayer Ag Process for the purification of polyisocyanates
EP0133538A3 (en) * 1983-08-11 1987-12-16 Bayer Ag Process for the purification of polyisocyanates, and the polyisocyanates so purified

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