GB941486A - Improvements in or relating to a process for the manufacture of hydrocyanic acid - Google Patents

Improvements in or relating to a process for the manufacture of hydrocyanic acid

Info

Publication number
GB941486A
GB941486A GB2518360A GB2518360A GB941486A GB 941486 A GB941486 A GB 941486A GB 2518360 A GB2518360 A GB 2518360A GB 2518360 A GB2518360 A GB 2518360A GB 941486 A GB941486 A GB 941486A
Authority
GB
United Kingdom
Prior art keywords
methane
mixture
oxygen
ammonia
hydrocarbon
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
GB2518360A
Inventor
John Benjamin Warren
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 GB2518360A priority Critical patent/GB941486A/en
Priority to DEJ20285A priority patent/DE1173444B/en
Publication of GB941486A publication Critical patent/GB941486A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01CAMMONIA; CYANOGEN; COMPOUNDS THEREOF
    • C01C3/00Cyanogen; Compounds thereof
    • C01C3/02Preparation, separation or purification of hydrogen cyanide
    • C01C3/0208Preparation in gaseous phase
    • C01C3/0212Preparation in gaseous phase from hydrocarbons and ammonia in the presence of oxygen, e.g. the Andrussow-process
    • C01C3/0216Preparation in gaseous phase from hydrocarbons and ammonia in the presence of oxygen, e.g. the Andrussow-process characterised by the catalyst used

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Inorganic Chemistry (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Hydrocyanic acid is prepared by the passage of a mixture comprising ammonia, a hydrocarbon such as methane, or a mixture of hydrocarbons, and oxygen in the vapour phase, at an elevated temperature, through one or more layers of a platinum or platinum alloy gauze catalyst, which has been activated by passing a mixture comprising ammonia, a hydrocarbon such as methane, or a mixture of hydrocarbons, and oxygen through the catalyst together with a volatile sulphidic material, in amount equivalent to 2 to 200 mg. s./m.3 at S.T.P., for at least one hour at an elevated temperature immediately before use. "A hydrocarbon such as methane or a mixture of hydrocarbons" refers to methane or mixtures of methane with a lesser proportion of its homologues, e.g. ethane, propane and butane. The preferred ratios of hydrocarbon to ammonia is 0.7 : 1 to 1.8 : 1, of oxygen to ammonia is 0.7 : 1 to 1.8 : 1 and the oxygen content is adjusted for maximum conversion of ammonia during the activation period, which is usually 1 to 2 hours. Either free oxygen or air may be used. Normal working temperatures are 700 DEG to 1250 DEG C. and the catalyst is not allowed to cool between activation and production of hydrocyanic acid. Suitable sulphidic material includes carbon disulphide, thiophene, hydrogen sulphide, methyl-, ethyl-, propyl- and butyl-mercaptans and dimethyl and diethyl sulphides. Examples are given using 90/10 platinum/rhodium alloy with a sulphur free mixture of 70% methane and 30% hydrogen and with a C : NH3 ratio of 1 : 1 using both air and oxygen with and without volatile sulphidic materials.
GB2518360A 1960-07-25 1960-07-25 Improvements in or relating to a process for the manufacture of hydrocyanic acid Expired GB941486A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB2518360A GB941486A (en) 1960-07-25 1960-07-25 Improvements in or relating to a process for the manufacture of hydrocyanic acid
DEJ20285A DE1173444B (en) 1960-07-25 1961-07-21 Process for the production of hydrogen cyanide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2518360A GB941486A (en) 1960-07-25 1960-07-25 Improvements in or relating to a process for the manufacture of hydrocyanic acid

Publications (1)

Publication Number Publication Date
GB941486A true GB941486A (en) 1963-11-13

Family

ID=10223586

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2518360A Expired GB941486A (en) 1960-07-25 1960-07-25 Improvements in or relating to a process for the manufacture of hydrocyanic acid

Country Status (2)

Country Link
DE (1) DE1173444B (en)
GB (1) GB941486A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2928910A1 (en) * 2008-03-20 2009-09-25 Arkema France IMPROVED PROCESS FOR THE PRODUCTION OF CYANHYDRIC ACID

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2928910A1 (en) * 2008-03-20 2009-09-25 Arkema France IMPROVED PROCESS FOR THE PRODUCTION OF CYANHYDRIC ACID
FR2928911A1 (en) * 2008-03-20 2009-09-25 Arkema France IMPROVED PROCESS FOR THE PRODUCTION OF CYANHYDRIC ACID
WO2009125101A1 (en) * 2008-03-20 2009-10-15 Arkema France Improved process for producing hydrocyanic acid
AU2009235293B2 (en) * 2008-03-20 2011-06-16 Arkema France Improved process for producing hydrocyanic acid

Also Published As

Publication number Publication date
DE1173444B (en) 1964-07-09

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