GB394689A - Improvements in or relating to the manufacture of aliphatic anhydrides - Google Patents

Improvements in or relating to the manufacture of aliphatic anhydrides

Info

Publication number
GB394689A
GB394689A GB3603031A GB3603031A GB394689A GB 394689 A GB394689 A GB 394689A GB 3603031 A GB3603031 A GB 3603031A GB 3603031 A GB3603031 A GB 3603031A GB 394689 A GB394689 A GB 394689A
Authority
GB
United Kingdom
Prior art keywords
barium
catalysts
nickel
potassium
preheated
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
GB3603031A
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.)
Henry Dreyfuss Associates LLC
Original Assignee
Henry Dreyfuss Associates LLC
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 Henry Dreyfuss Associates LLC filed Critical Henry Dreyfuss Associates LLC
Priority to GB3603031A priority Critical patent/GB394689A/en
Publication of GB394689A publication Critical patent/GB394689A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/54Preparation of carboxylic acid anhydrides
    • C07C51/56Preparation of carboxylic acid anhydrides from organic acids, their salts, their esters or their halides, e.g. by carboxylation

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Catalysts (AREA)

Abstract

Aliphatic anhydrides such as the anhydrides of acetic, propionic, and alkoxy-fatty acids are produced by thermal decomposition of the corresponding acids in presence of catalysts comprising a phosphoric acid combined with a plurality of metals at least one of which is at least as electronegative as barium. The metal may be present as basic or acid radicals. A large number of double ortho, meta and pyrophosphates are mentioned, including alkalialkaline earth phosphates, alkali and alkaline earth-aluminium phosphates, purpureo and luteo potassium vanadium phosphates, potassium-antimony, barium-aluminium, calcium and copper phosphotungstates, barium, nickel and cobalt phospho-molybdates and magnesium-nickel, zinc-nickel and zinc-cobalt phosphates. By heating some of these compounds, especially mono- or di-metaphosphates, complex polymetaphosphates may be made. The treatment of the acid vapour may be effected by passing it through liquid or molten baths consisting of or containing the catalysts, and salts or other substances of low melting-point may be used to dissolve or suspend the catalysts. Suitable substances of this kind are mixtures of sodium and potassium chlorides or of calcium and magnesium or barium chlorides, or metals, such as lead, or tellurium, or alloys thereof. Or the acid vapour may be passed through tubes containing the catalysts, which may be supported upon carriers or filling materials, or in admixture with other catalysts for the reaction. Or the liquid acids containing the catalysts may be sprayed into a hot reaction zone. The acids may be preheated to or near the reaction temperature. The anhydride may be separated from the reaction vapour by the processes of Specifications 256,663, 279,916, 289,972, 298,667, 303,772 or 310,863, [all in Class 2 (iii), Dyes &c.]. In examples: (1) acetic acid vapour is preheated to 500 DEG C. and passed through molten sodium and potassium chlorides containing potassium barium tetrametaphosphate at 700 DEG C.; (2) propionic acid vapour preheated to 530 DEG C., is passed over a catalyst prepared by impregnating pumice with a solution of sodium tungstate and disodium phosphate neutralized with acetic acid, and then treating the mass with a solution of barium chloride, and if desired washing to remove sodium chloride; (3) nickel phosphomolybdate, prepared by treating nickel phosphate with molybdic oxide is first heated at 200 DEG C. and is suspended in glacial acetic acid which is preheated under 10 atmospheres pressure at 200 DEG C. and sprayed into a copper-lined reaction chamber at 700 DEG C.ALSO:Aliphatic anhydrides, such as the anhydrides of acetic, propionic, and alkoxy-fatty acids are produced by thermal decomposition of the corresponding acids in presence of catalysts comprising a phosphoric acid combined with a plurality of metals at least one of which is at least as electronegative as barium. The metal may be present as basic or acid radicals. A large number of double ortho, meta and pyrophosphates are mentioned, including alkali-alkaline earth phosphates, alkali and alkaline earth-aluminium phosphates, purpureo and luteo potassium vanadium phosphates, potassium-antimony, barium-aluminium, calcium and copper phosphotungstates, barium, nickel and cobalt phospho-molyddates and magnesium nickel, zinc-nickel and zinc-cobalt phosphates. By heating some of these compounds, especially mono- or di-metaphosphates, complex polymetaphosphates may be made. The treatment of the acid vapour may be effected by passing it through liquid or molten baths consisting of or containing the catalysts, and salts or other substances of low melting point may be used to dissolve or suspend the catalyst. Suitable substances of this kind are mixtures of sodium and potassium chlorides or of calcium and magnesium or barium chlorides, or metals such as lead, or tellurium, or alloys thereof. Or the acid vapour may be passed through tubes containing the catalysts, which may be supported upon carriers or filling materials, or in admixture with other catalysts for the reaction. Or the liquid acids containing the catalysts may be sprayed into a hot reaction zone. The acids may be preheated to or near the reaction temperature. The anhydride may be separated from the reaction vapour by the processes of Specifications 256,663, 279,916, 289,972, 298,667, 303,772, or 310,863, [all in Class 2 (iii), Dyes &c.]. In examples (1) Acetic acid vapour is preheated to 500 DEG C. and passed through molten sodium and potassium chlorides containing potassium barium tetrametaphosphate at 700 DEG C.; (2) propionic acid vapour, preheated to 550 DEG C. is passed over a catalyst prepared by impregnating pumice with a solution of sodium tungstate and disodium phosphate neutralized with acetic acid, and then treating the mass with a solution of barium chloride, and if desired washing to remove sodium chloride; (3) nickel phosphomolybdate, prepared by treating nickel phosphate with molybdic oxide is first heated at 200 DEG C. and is suspended in glacial acetic acid which is preheated under 10 atmospheres pressure at 200 DEG C. and sprayed into a copper-lined reaction chamber at 700 DEG C.
GB3603031A 1931-12-31 1931-12-31 Improvements in or relating to the manufacture of aliphatic anhydrides Expired GB394689A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3603031A GB394689A (en) 1931-12-31 1931-12-31 Improvements in or relating to the manufacture of aliphatic anhydrides

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3603031A GB394689A (en) 1931-12-31 1931-12-31 Improvements in or relating to the manufacture of aliphatic anhydrides

Publications (1)

Publication Number Publication Date
GB394689A true GB394689A (en) 1933-06-30

Family

ID=10384179

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3603031A Expired GB394689A (en) 1931-12-31 1931-12-31 Improvements in or relating to the manufacture of aliphatic anhydrides

Country Status (1)

Country Link
GB (1) GB394689A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2745833A (en) * 1950-05-29 1956-05-15 Phillips Petroleum Co Production of substituted pyridiens

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2745833A (en) * 1950-05-29 1956-05-15 Phillips Petroleum Co Production of substituted pyridiens

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