GB280712A - Improvements in the regeneration of catalysts - Google Patents

Improvements in the regeneration of catalysts

Info

Publication number
GB280712A
GB280712A GB2996026A GB2996026A GB280712A GB 280712 A GB280712 A GB 280712A GB 2996026 A GB2996026 A GB 2996026A GB 2996026 A GB2996026 A GB 2996026A GB 280712 A GB280712 A GB 280712A
Authority
GB
United Kingdom
Prior art keywords
air
treated
mass
oxidation
contact mass
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
GB2996026A
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.)
Selden Co
Original Assignee
Selden 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 Selden Co filed Critical Selden Co
Priority to GB2996026A priority Critical patent/GB280712A/en
Publication of GB280712A publication Critical patent/GB280712A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J38/00Regeneration or reactivation of catalysts, in general

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

Abstract

280,712. Fairweather, H. G. C., (Selden Co.). Nov. 26, 1926. Formaldehyde ; benzaldehyde ; acetic acid; maleic acid ; benzoic acid ; phthalic anhydride; naphthalic anhydride ; benzoquinone; a-naphthaquinone ; anthraquinone phenanthraquinone ; acenaphthaquinone. - Catalysts which have deteriorated through use in the catalytic oxidation of organic compounds are regenerated by treatment with one or more of the following reagents, viz., a halogen, a non-metallic halogen compound, a non-metallic acid or its anhydride, ozone, or hydrogen peroxide, the regenerating agent being such that it is volatile below about 550‹ C., and does not decompose and leave a residue which, when treated with oxygen at an elevated temperature, is not volatile; the regenerating agents may be used in admixture with steam. Generally, the catalyst is treated simultaneously or subsequently with oxygen-containing gases at an elevated temperature, but this treatment may be omitted when the regenerating agent is such that it decomposes with the production of oxygen. The catalyst may be treated in situ and the treatment may be performed at any desired pressure. In one example, a contact mass comprising silver vanadate, potassium sulphate, and kieselguhr is used at 340-420‹ C. in the production of phthalic anhydride from a mixture of naphthalene and air, and is regenerated by mixing sulphur dioxide with the naphthalene-air mixture. Alternatively the spent contact mass may be treated first with air and then with a mixture of sulphur dioxide and air, with or without steam at 350-500‹ C., or it may be treated in turn with air and sulphur trioxide at a temperature below 200‹ C. and then with air alone at 350-500‹ C. A further alternative consists in substituting for the sulphur dioxide, wholly or in part, nitric acid vapours or gases containing nitrogen oxides, which may be used at any temperature up to 500‹ C. and with or without air or steam. In another example, a contact mass comprising iron vanadate, iron molybdates, and pumice, after use in the oxidation of acenaphthene 'to naphthalic anhydride, is treated first with chlorine at ordinary temperature and then with air, with or without steam, at 200-500‹ C. Alternatively, the regeneration may be effected with a mixture of chlorine and air, or ethylene chloride and air, at 300-500‹ C., or the reagents of the preceding example may be employed. In a further example, a contact mass comprising nickel molybdate, calcium chloride, and pumice, after use in the production of formaldehyde from methyl alcohol, is treated first with a current of air containing nitrosyl chloride and then with air alone. The treatment mav be effected at ordinary temperature or, if the contact mass is contaminated with carbon, at 300-500‹ C. Alternatively, the mass may be regenerated by treating it first with phosgene at 200‹ C. and then with air at 400- 500‹ C. This treatment with phosgene and air is used, according to another example, in the regeneration of a contact mass, prepared by treating granules of ferrosilicon with an aqueous solution of ammonium vanadate, evaporating the mixture, and heating it to 400-450‹ C., the mass having become spent in the oxidation of naphthalene to phthalic anhydride. A further example describes the regeneration of a contact mass comprising iron vanadate, cobalt molybdate, potassium sulphate, and pumice after use in the oxidation of anthracene to anthraquinone. The mass is heated in air or oxygen at 300-450‹ C. and is then cooled and treated at ordinary temperature with an aqueous solution of hydrogen peroxide, whereafter the water is evaporated. In another example, a contact mass comprising silver vanadate and aluminium, after use in the oxidation of benzene to maleic acid or of methyl alcohol to formaldehyde, is treated with ozonized air at a temperature gradually @ising to 300‹ C. In the final example, a contact mass for use in the oxidation of naphthalene to phthalic anhydride is prepared by the interaction of a sodiumsilicate solution containing cellite and solutions of potassium vanadate and potassium aluminate, the zeolitic product being treated with sulphuric acid and than calcined in air at 300-400‹ C. The mass is regenerated after use by treatment with a mixture of sulphur dioxide and/or chlorine and air at 200-500‹ C. The regeneration of other polysilicate catalysts and of catalysts comprising the oxides or other compounds of the elements of the fifth, sixth, and seventh groups of the periodic system is referred to, and, as further instances of reactions in which the ' catalysts may have become spent, reference is made 'to the oxidation of naphthalene to a-naphthaquinone or maleic acid, of toluene or phenol to maleic acid, of benzene or phenol to benzoquinone, of toluene and its substitution products and derivatives to the corresponding aldehydes and acids, of acenaphthene to acenaphthaquinone. of phenanthrene to phenanthraquinone, and of ethyl alcohol to acetic acid. Mention is made also, as additional regenerating agents, of hydrogen halides, ammonium halides, sulphur chloride, sulphuryl chloride, thionyl chloride, chlorinated aromatic hydrocarbons, acyl halides, and ethylene bromide.
GB2996026A 1926-11-26 1926-11-26 Improvements in the regeneration of catalysts Expired GB280712A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2996026A GB280712A (en) 1926-11-26 1926-11-26 Improvements in the regeneration of catalysts

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2996026A GB280712A (en) 1926-11-26 1926-11-26 Improvements in the regeneration of catalysts

Publications (1)

Publication Number Publication Date
GB280712A true GB280712A (en) 1927-11-24

Family

ID=10299994

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2996026A Expired GB280712A (en) 1926-11-26 1926-11-26 Improvements in the regeneration of catalysts

Country Status (1)

Country Link
GB (1) GB280712A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2758097A (en) * 1952-11-04 1956-08-07 Socony Mobil Oil Co Inc Reactivation of metal-poisoned catalysts
US2764557A (en) * 1952-11-04 1956-09-25 Socony Mobil Oil Co Inc Reactivation of metal-poisoned catalysts
US3086994A (en) * 1957-08-01 1963-04-23 Consortium Elektrochem Ind Process for the production of aldehydes and ketones
US3121673A (en) * 1957-07-10 1964-02-18 Hoechst Ag Process of regenerating a liquid catalyst
US3247128A (en) * 1961-09-11 1966-04-19 British Petroleum Co Regeneration of catalysts
US4882039A (en) * 1986-12-04 1989-11-21 Mobil Oil Corporation Catalytic cracking of hydrocarbons with oxygen promoted alkali metal zeolite cracking catalyst

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2758097A (en) * 1952-11-04 1956-08-07 Socony Mobil Oil Co Inc Reactivation of metal-poisoned catalysts
US2764557A (en) * 1952-11-04 1956-09-25 Socony Mobil Oil Co Inc Reactivation of metal-poisoned catalysts
US3121673A (en) * 1957-07-10 1964-02-18 Hoechst Ag Process of regenerating a liquid catalyst
US3086994A (en) * 1957-08-01 1963-04-23 Consortium Elektrochem Ind Process for the production of aldehydes and ketones
US3247128A (en) * 1961-09-11 1966-04-19 British Petroleum Co Regeneration of catalysts
US4882039A (en) * 1986-12-04 1989-11-21 Mobil Oil Corporation Catalytic cracking of hydrocarbons with oxygen promoted alkali metal zeolite cracking catalyst

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