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Publication numberUS3077488 A
Publication typeGrant
Publication dateFeb 12, 1963
Filing dateMar 12, 1959
Priority dateMar 12, 1959
Publication numberUS 3077488 A, US 3077488A, US-A-3077488, US3077488 A, US3077488A
InventorsRobert M Mercier, Yoland P P Mayor, Bieselaar Dirk
Original AssigneeRobert M Mercier, Yoland P P Mayor, Bieselaar Dirk
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Method of oxidizing ferrous salts into ferric salts in the presence of a gas containing free oxygen
US 3077488 A
Abstract  available in
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Description  (OCR text may contain errors)

e present invention relates to a method of oxidizing ferrous salts into ferric salts in the presence of air, products obtained thereby and applications thereof.

it is a well-known fact that ferric salts form oxidizing agents which are of considerable interest for the solving of numerous problems, both of inorganic and of organic chemistry. They allow for instance transforming mercaptans into bisulfides, o-nitrobenzaldoxime into o-nitrobenzoic aldehyde, indoxyl into indigo, phenylhydrazoaldoximes into azo derivatives, hydrogen sulfide into sulfur and the like.

When used for such applications, the ferric salts are reduced into ferrous salts and it is obvious that the use of ferric salts as oxidizing reagents would be of a considerable interest if it were possible to regenerate the ferrous salts thus obtained into ferric salts. It is known furthermore that ferrous salts are transformed in the presence of air into ferric salts through an oxidizing reaction which may be Written out for instance:

It is one object of the present invention to provide a method which relates to the obtention of ferric salts the reduction of which leads to the formation of ferrous salts which are readily regenerated, so as to return into the state of ferric salts.

Our improved method resides in the following features:

If we add to a solution of ferrous salts certain organic amino-acids such as those which are obtained through the controlled hydrolysis of albuminoid substances and if air is caused to pass through the solution, there is obtained a sparingly soluble ferric salt which separates out of the liquid phase as it is being formed, which prevents the oxidation reaction from being limited by chemical equilibrium. The ferric salt separates out as a highly subdivided deposit and there is obtained finally a suspension which may serve as an oxidizing agent to the same extent and in the same manner as a solution of a ferric chloride, sulfate or the like salt.

In particular, if it is desired to treat such a suspension with sulfuretted hydrogen, the iron redissolves and forms a ferrous compound, while the sulfur is precipitated. The amino-acid is redissolved together with the iron. It may be assumed Without this theory limiting by any means the scope of the present invention that the following reactions are obtained:

Oxidation: FeX +HOOC.R.NI-I AO Amino-acid =FeX OC.R.NH /2H O Insoluble complex salt (the atoms of iron and nitrogen in the complex salt being probably bound together through a covalence).

Reduction: FeX .OOC.R.NH +%H S=FeX +I-IOOC.R.NH +%S (X=Cl, V280 etc.)

When applying this method, it is possible to resort to various amino-acids, those obtained through partial hydrolysis of albuminoid substances such as albumin, globulin, gelatine, keratin, etc. The hydrolysis may be 3,977,488 Patented Feb. 12, 1953 performed through the action of an acid, an alkaline substance or an enzyme on the albuminoid material. It is to be understood, however, that the reference to aminoacids means conventional amino-acids and not, for instance, hydroxy-amino acids.

Inorcler that the oxidizing reaction of the ferrous salt may be obtained speedily, it is necessary to provide for an intimate contact between the solution offerrous salt and oxygen.

This may be obtained by introducing air through a porous plate or else by resorting to a column including a filling and in which the solution flows downwardly and the air upwardly, etc. Excellent results have been obtained particularly through the incorporation of air into a solution of a ferrous salt to obtain a finebubbled froth remaining stable for a time sufficient for the oxidation to be performed. It is possible, to this end, to introduce into the solution a reagent adapted to modify the surface pressure of the latter without reacting on the iron salts. But it is also possible to use an amino-acid constituted by a derivative having a large frothing power, for instance a substance obtained through alkaline hydrolysis of wool or comminuted horn material which allows resorting to the same reagent both for the insolubilization of the ferric ions and for the obtention of frothing properties in the solution.

EXAMPLE A mixture is prepared which contains 10% by weight of ferrous sulfate and 5% by volume of a solution obtained through alkaline hydrolysis or hydrolysis with calcium hydroxide of comminuted horn material after which the solution is neutralized with sulfuric acid and filtered. The mixture comprising a solution containing 20% of dry material is caused to froth to an extent such that 100 cu. cm. supply 3 liters of froth. Said froth is kept at 40 C. during ten minutes, after which it is urged into a mechanical froth breaker to be destroyed therein.

We obtain thus a suspension of the ferric salt and analysis shows that of the ferrous ions are transformed into ferric ions.

The suspension of a ferric compound thus obtained may serve for executing various organic or inorganic oxidations. If care is taken to select a stable amino-acid such as that obtained through hydrolysis of comminuted horn material, it may be regenerated indefinitely.

It is possible, in particular, to resort to such a suspen* sion for the oxidation of sulfuretted hydrogen into sulfur and it should be remarked that it is not necessary in such a case to oxidize concentrated sulfuretted hydrogen.

It is also possible to treat through an excess amount of a suspension of a ferric salt industrial gases contain ing sulfuretted hydrogen and, in such a case, the gas is completely stripped of its sulfur and We obtain a suspension of sulfur in a solution of a ferrous salt and of an amino-acid. Said sulfur may be recovered through any known method such as filtration, centrifugation, extraction through a solvent, melting under pressure and the like, said means being applied separately or in combination. The ferric reagent is then regenerated through oxidation by air.

While we have disclosed several embodiments of the present invention, it is to be understood that these embodiments are given by example only and not in a limiting sense, the scope of the present invention being determined by the objects and the claims.

What we claim is:

1. A method of oxidizing inorganic ferrous salts into ferric salts comprising the steps of adding to a solution of said ferrous salts an amino-acid containing a carboxylic group and an amino group connected with the same carbon atom,

subjecting said solution to a gas containing free oxygen, References Cited in the file of this patent resulting in soluble ferrous salts and in insoluble ferric salts, thereby obtaining an aqueous suspension UNITED STATES PATENTS of insoluble ferric salts, to function as an oxidizing 1 13 stall et 1 15 19 2 reagent 5 2,462,124 N b t 1 F b. 2 49 2. The method, as set forth in claim 1, which includes 2 772 146 i g g e a 3 as the step of subjecting said solution to a gas contain- 2819950 Patton 1958 ing free oxygen, the steps of u forming a froth consisting of finebubbles, the liquid g et a1 i phase of which consists of said aqueous solution of 10 P ermann ferrous salts and said amino acid, OTHER REFERENCES the gaseous phase of which consists of said oxygen containing gas, and King et al.: The Fundamentals of College Chemistrv,

breaking said froth upon terminating the oxidation. 2nd edition Pages 222, 223 and

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US1888186 *Nov 5, 1931Nov 15, 1932Firm Of Chemical Works FormerlComplex glucosaminic acid salts of the metals of the iron group
US2462124 *Jan 19, 1946Feb 22, 1949Interchem CorpManufacture of amino acids
US2772146 *Sep 29, 1952Nov 27, 1956Heinz PippigProcess for the recovery of elementary sulfur from gases containing hydrogen sulfide
US2819950 *Mar 27, 1952Jan 14, 1958Texas Gulf Sulphur CoConversion of hydrogen sulfide to sulfur with quinones
US2831885 *Aug 13, 1954Apr 22, 1958Geigy Chem CorpHydroxyethyl polycarboxymethyl polyamines
US2890233 *Oct 13, 1952Jun 9, 1959Josef Opfermann Adolf ChristiaIron-containing organic compounds
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3607069 *Dec 9, 1969Sep 21, 1971Allied ChemProcess for recovering sulfur and metal values from sulfur-bearing minerals
US3622273 *Feb 6, 1970Nov 23, 1971Nalco Chemical CoMethod for the removal of hydrogen sulfide from gaseous streams
US3650889 *Aug 3, 1970Mar 21, 1972Combustion EngPollution controlled polysulfide recovery process
US3676356 *Mar 22, 1971Jul 11, 1972Nalco Chemical CoComposition for the removal of hydrogen sulfide from gaseous streams
US4243648 *Jun 20, 1979Jan 6, 1981Union Oil Company Of CaliforniaMethod for removing hydrogen sulfide from gas streams
US4374104 *Sep 30, 1980Feb 15, 1983Air Resources, Inc.Composition and method for removing hydrogen sulfide from gas stream
US4649032 *Jan 11, 1985Mar 10, 1987Mobil Oil CorporationProcess for the selective removal of hydrogen sulfide from gaseous streams
US4859436 *Jul 16, 1987Aug 22, 1989Shell Oil CompanyH2 S removal process and composition
US4871520 *Jul 16, 1987Oct 3, 1989Shell Oil CompanyProcess and composition for H2 S removal
US5149460 *Sep 18, 1991Sep 22, 1992Shell Oil CompanyComposition for H2 S removal
Classifications
U.S. Classification556/139, 423/226, 556/148, 423/576.6, 423/DIG.140
International ClassificationC01G49/00
Cooperative ClassificationC01G49/00, Y10S423/14
European ClassificationC01G49/00