[go: up one dir, main page]

GB252327A - Oxidized products, processes of making same, and apparatus therefor - Google Patents

Oxidized products, processes of making same, and apparatus therefor

Info

Publication number
GB252327A
GB252327A GB5908/26A GB590826A GB252327A GB 252327 A GB252327 A GB 252327A GB 5908/26 A GB5908/26 A GB 5908/26A GB 590826 A GB590826 A GB 590826A GB 252327 A GB252327 A GB 252327A
Authority
GB
United Kingdom
Prior art keywords
oil
oils
air
treated
per cent
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
GB5908/26A
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.)
WILLIAM BOSE DOBBIN PENNIMAN
Original Assignee
WILLIAM BOSE DOBBIN PENNIMAN
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 WILLIAM BOSE DOBBIN PENNIMAN filed Critical WILLIAM BOSE DOBBIN PENNIMAN
Publication of GB252327A publication Critical patent/GB252327A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C27/00Processes involving the simultaneous production of more than one class of oxygen-containing compounds
    • C07C27/10Processes involving the simultaneous production of more than one class of oxygen-containing compounds by oxidation of hydrocarbons

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

252,327. Penniman, W. B. D. May 20, 1925, [Convention date]. Mineral and tar oils and waxes, purifying etc.; motor spirit; fats, extracting by solvents.-Crude petroleum and its distillates, shale oils and tars, waxes, sludges, petroleum residues, asphaltic oils, asphalt., malthas, cracked oils and residues from cracking-stills, wood tar oils and wood tar, peat and lignite distillates, coal tar oils and coal tars, and oils containing powdered coal. coke or peat, sulphur &c. in suspension, are oxidized to yield motor fuels, burning oils, aldehydes, fatty acids, alcohols, ketones, solvents, gums &c., by passing air or other oxygen-containing gas under pressure through a heated layer of the material of a depth sufficient substantially to deoxygenate the air &c.. the material being in the liquid state or suspended in a suitable liquid carrier. The oxidizing gas may be enriched with oxygen or diluted with steam. The process is preferably carried out at a temperature of 60-900‹ F., though the tem. perature range may extend from 300 to 1,000‹ F. Catalysts such as aluminium chloride, the oxides of manganese, lead, iron, chromium, vanadium, zinc, copper, or calcium may be added, and also neutralizing agents such as quick lime. limestone, or alkaline carbonates. The depth of the oil layer under treatment is preferably maintained substantially constant, as by intermittently or continuously feeding fresh oil to, and withdrawing treated oil from, the reactions chamber. Baffles may be provided in the reactions chamber to impede the passage of air therethrough, to assist the circulation of the oil, or to cause any separated solid, such as carbon, to be deposited in a desired part of the apparatus. The reaction chamber may be externally heated, or the oil &c. and air &c. may be preheated, and the temperature in the chamber be maintained solely by the heat of reaction. The oxidation and disintegration products of the oils &c. removed by the current of air &c. are condensed with or without pressure, and the deoxygenated air may be passed through silica gel or absorbent carbon to extract residual vapour. As shown in Fig. 1, the apparatus for carrying out the process may comprise a vertical still 1 adapted to be heated by a gas fired furnace, a condenser tube and coil 24, 25, and a receiver 26, the members 24 - - 26 being preferably con. structed of copper, chromium or nickel chrome steel, morel metal, or other acid-resisting material; or enamel lined condenser tubes may be employed. Oil is supplied to the still by a pump 5, pipe 6, coil 12, and pipe 8, and air by a pump 9, pipe 10. coil 7, and pipe 13 having at its lower end an upwardly directed nozzle, 14, or a series of radially extending perforated pipes. More than one air supply line may be provided, and a battery of stills may be employed, each being fitted at its upper part with a dephlegmator and heat interchanger. Residual material may be withdrawn by a pipe 10. In an example, a mid-continentle gas oil was treated at 500‹ F. under 300 1bs. pressure, air being supplied at 300 cubic feet per minute under a pump pressure of 350 1bs. The temperature during treatment rose to and was maintained at 725-750‹ F. The distillate obtained was run into a wooden tank, and separated. on standing, into an upper water-insoluble layer, an intermediate mixed layer, and a lower layer containing a water solution of organic substances. Any water soluble constituents in the upper layer were washed out with water. From the upper layer, acids, phenols, aldehydes &c. may be removed by agitation with a ten per cent solution of caustic soda or acids may first be removed by sodium carbonate, solution, and aldehydes and phenols then be separated by caustic soda; or aldehyde may first be removed by a concentrated solution of sodium bisulphate, which may be produced from the sulphur dioxide formed during the.process, when a sulphur-bearing oil is treated. The material remaining after the treatment with caustic soda may be washed with water, treated with a small amount of sulphuric acid, and' distilled, the distillates up to 400‹ F., which may contain up to three per cent of oxygen, being used as a gasoline substitute; or they may be mixed with ordinary gasoline, benzol, acetone &c. The residues from the distillation may be returned to the still for further treatment. From the sludge obtained by the treatment with sulphuric acid, alcohols may be recovered by diluting the sludge with water and then steam stilling it. The upper layer may be first purified by passage through fuller's earth, silica gel, or heated bauxite; or it may be redistilled with aluminium chloride; or it may, following the treatment with sodium carbonate or caustic soda, be distilled with five per cent of aniline or with phenol to separate aldehyde. The caustic soda solution from the distillate may be acidified and steam stilled to isolate the volatile fatty acids and phenloid bodies, which are then separated by sodium carbonate. The lower water soluble layer of the distillates, containing about three per cent of acids, mainly acetic acid. seven per cent of aldehydes, mainly acetaldehyde and propionaldehyde. three per cent of ketones, and five per cent of alcohols was subjected to distillations in twelve fractions between 20‹ and 95‹ C. The first two fractions were mainly acetaldehyde; the last nine were treated with caustic soda and redistilled. whereby a liquid of boiling point range 40-85‹ C. was obtained, which may be added to gasoline or kerosene to give. it antiknock properties, or for the extraction of fats. The residue from this distillation may be treated with sulphuric acid and steam stilled, the gummy residue being either used for making gums, or being combined with aniline, hydrozine or phenol. The oil &c. withdrawn from the still during the process may be treated to recover fatty acids, or may be returned to the still. Before treatment, the oil &c. may be chlorinated, nitrated, sulphated, &c. The Specification as open to inspection under Sect. 91 (3) (a) comprises also the carrying out of the process at atmospheric pressure. This subject-matter does not. appear in the Specification as accepted. Reference has been, directed by the Comptroller to Specifications 16182/05 and 131,303.
GB5908/26A 1925-05-20 1926-03-02 Oxidized products, processes of making same, and apparatus therefor Expired GB252327A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US252327XA 1925-05-20 1925-05-20

Publications (1)

Publication Number Publication Date
GB252327A true GB252327A (en) 1927-09-02

Family

ID=21824819

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5908/26A Expired GB252327A (en) 1925-05-20 1926-03-02 Oxidized products, processes of making same, and apparatus therefor

Country Status (1)

Country Link
GB (1) GB252327A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5225159A (en) * 1991-12-13 1993-07-06 Henry Sawatzky Deodorization of sewage sludge-derived oils
CN112158884A (en) * 2020-09-25 2021-01-01 甘肃锦世化工有限责任公司 Method for improving color of chromium oxide green

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5225159A (en) * 1991-12-13 1993-07-06 Henry Sawatzky Deodorization of sewage sludge-derived oils
CN112158884A (en) * 2020-09-25 2021-01-01 甘肃锦世化工有限责任公司 Method for improving color of chromium oxide green

Similar Documents

Publication Publication Date Title
US2413945A (en) Treating petroleum distillates
US2201050A (en) Process for producing carbonaceous material
GB252327A (en) Oxidized products, processes of making same, and apparatus therefor
US1995324A (en) Oxidizing petroleum and the products thereof
US1847597A (en) Treatment of crude pyroligneous acid
US2007212A (en) Process for treating oils
US2112250A (en) Process of making oxidized products
US2044014A (en) Process of making oxidized products
US2163227A (en) Process for desulphurizing alkyl phenols
GB256922A (en) Oxidized products, processes of making same, and apparatus therefor
GB255020A (en) Oxidized products, processes of making same, and apparatus therefor
US2132968A (en) Motor fuel
US1517968A (en) Cracking and oxidizing petroleum oil to make gasoline and useful products of oxidation
US2203217A (en) Process for recovering alkyl phenols from petroleum oils
US1801213A (en) Process of refining mineral oils
US1936570A (en) Gas purification
US2176655A (en) Continuous method of cracking hydrocarbon oil
US2050772A (en) Process of refining mineral oil
US2200711A (en) Process for the refining of naphthenic acids
US1697266A (en) Process of cracking and oxidizing oils
US2040101A (en) Treatment of tar
US2070256A (en) Method for making a sulphur bearing oil
US1981614A (en) Method for deriving liquid hydrocarbons from solid carbonizable materials
US2200703A (en) Process for refining hydrocarbon oils
US1988083A (en) Process for refining hydrocarbon oil