US2289258A - Process for the manufacture of iron oxide - Google Patents

Process for the manufacture of iron oxide Download PDF

Info

Publication number
US2289258A
US2289258A US299761A US29976139A US2289258A US 2289258 A US2289258 A US 2289258A US 299761 A US299761 A US 299761A US 29976139 A US29976139 A US 29976139A US 2289258 A US2289258 A US 2289258A
Authority
US
United States
Prior art keywords
hydroxide
ferrous
ferric
electrolysis
iron oxide
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 - Lifetime
Application number
US299761A
Inventor
French Thomas Glenwright
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.)
PRIESTMAN COLLIERIES Ltd
Original Assignee
PRIESTMAN COLLIERIES 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 PRIESTMAN COLLIERIES Ltd filed Critical PRIESTMAN COLLIERIES Ltd
Application granted granted Critical
Publication of US2289258A publication Critical patent/US2289258A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09CTREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C1/00Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/22Compounds of iron
    • C09C1/24Oxides of iron
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G49/00Compounds of iron
    • C01G49/02Oxides; Hydroxides
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/60Optical properties, e.g. expressed in CIELAB-values
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/80Compositional purity
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S423/00Chemistry of inorganic compounds
    • Y10S423/01Waste acid containing iron
    • Y10S423/02Sulfuric acid

Definitions

  • This invention relates to processes for the manufacture of iron oxide of the kind comprising precipitating a ferrous hydroxide by the electrolysis with iron electrodes of a solution of ionizable alkaline metal salts such as sodium and/or potassium salt.
  • the object of the invention is to provide a process for the manufacture of iron oxide for use mainly as a black, brown or red pigment of According to one process an electrolyte of 'sodium chloride or sodium sulphate of density sp. gr. 1.10 is introduced into wood vats, into which are placed iron or mild steel anodes connected to a supply of D. C. current.
  • the electrolyte is maintained at a temperature of 80 to 90 C., and the current density is approximately .3 amp. per square inch.
  • the product after drying is a black hydroxide
  • the black hydroxide is calcined in q n y brought together Outside the electrolya suitable furnace with excess air, the degree of sis cell to precipitate the ferrous oxide which temperature affecting the resulting colour.
  • oxidised mother liquor example at 2Q0 C. a brown is obtained I have found that by Producing the iron oxide at 600 0.
  • a bright Turkey red is obtained, at electrolytically, a finer quality of pigment is ob- 00 a, deep Turkey red and at 10000 an tained than with chemical methods, and accorddian red pigment is produced.
  • the electrolytic me In drder to produce a maroon or ochre like eipiieiion 9 the 'PP hydroxlde 1S cqmbmed pigment in an alternative process the paste from the -o of the made the filter press is mixed with water to form a ciplta'Ped Whlle Stm m suspanslol ⁇ m the 6180' slurry.
  • an oxidizing agent, trolytic bath to produce a ferric-ferrous hypreferably a solution of sodium hypocmorite dmxide' m f t 4 which oxidizing agent is preferably made by In.add1t1n to the Q 0 plgmen 0 electrolysis of sodium chloride.
  • trolysis current is preferably reversed at inter- It 15 Important that the oxidizing ent be vals of about 30 minutes. Otherwise there is a introduced apart m t e ct o te. tendency for metallic iron coming down as black By calcining with excess of air as mentioned specks in connection with the first process a similar range of shades from light maroon or ochre to dark maroon may be obtained.
  • an electrolysis vat containing sodium chloride is connected in closed circuit with the mixing vat.
  • Sodium hypochlorite from the electrolysis vat is admitted to the mixing vat and at the same time the mixture in the mixing vat is subjected to boiling.
  • Sodium hypochlorite is continued to be admitted to the mixing vat until the required amount of oxidation has taken place as a result of the combined action of the 7 liquor in the mixing vat--which is sodium chloride,is pumped back to the electrolysis vat.
  • Ferric sulphate is now added to the paste in the mixing vat and boiling is continued until the ferric hydroxide ochre or ferrite pigment is obtained.
  • the pigment is then transferred to a second filter press, separated and washed anddried, and if desired calcined to temperatures depending on the depth of colour required.
  • iron oxide pigment from black to deep reds, maroons or ochres of a purity of 99.5% is obtained.
  • the process for producing maroon or ochre like pigments comprising precipitating ferrous hydroxide by the electrolysis with iron electrodes of a solution of an ionizable alkali metal salt, and oxidising the ferrous hydroxide precipitated while in suspension in the electrolysis bath to produce a ferric ferrous hydroxide, washing with water the ferric ferrous hydroxide, separating the said hydroxide, mixing the hydroxide. with water to form a slurry, adding an oxidising agent to said slurry, boiling the mixture until a ferric hydroxide of uniform light brown colour is obtained, then adding ferrous sulphate and continuing boiling until a ferric hydroxide ochre pigment known as ferrite is obtained.
  • the process for producing maroon or ochre like pigments comprising precipitating ferrous hydroxide by the electrolysis with iron electrodes of a solution of an ionizable alkali metal salt, and oxidising the ferrous hydroxide precipitated while in suspension in the electrolysis bath to produce a ferric ferrous hydroxide, washing with water the ferric ferrous hydroxide, separating the said hydroxide, mixing the hydroxide with water to form a slurry.'adding sodium hypochlorite to said slurry, boiling the mixture until a uniform light brown colour is obtained, then adding ferrous sulphate and continuing boiling until a ferric hydroxide ochre pigment known as ferrite is obtained.
  • the process for producing maroon or ochre like pigments comprising precipitating ferrous hydroxide by the electrolysis with iron electrodes of a solution of an ionizable alkali metal salt, and oxidising the ferrous hydroxide precipitated while in suspension in the electrolysis bath to produce a ferric ferrous hydroxide, washing with water the ferric ferrous hydroxide, separating the said hydroxide, mixing the hydroxide with water to form a slurry, adding to said slurry sodium hypochlorite which is obtained by the electrolysis of sodium chloride, the sodium hypochlorite giving up its oxygen during the first boiling and the resulting restored sodium chloride being used again in the electrolysis process for producing the sodium hypochlorite, the same sodium chloride thus being usable continually as an oxygen carrier for the oxidation step, boiling the mixture until a uniform light brown colour is obtained, then adding ferrous sulphate and continuing boiling until a ferric hydroxide ochre pigment known as ferrite is obtained.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Compounds Of Iron (AREA)

Description

Patented July 7, 1942 Thomas Glenwright French, Newcastle-on-Tyne, England, assignor to The Priestman Collieries Limited, Newcastle-on-Tyne, England, a British company No Drawing. Application October 16, 1939, Serial No. 299,761. In Great Britain September 30,
3 Claims. (01. 23-200) This invention relates to processes for the manufacture of iron oxide of the kind comprising precipitating a ferrous hydroxide by the electrolysis with iron electrodes of a solution of ionizable alkaline metal salts such as sodium and/or potassium salt.
The object of the invention is to provide a process for the manufacture of iron oxide for use mainly as a black, brown or red pigment of According to one process an electrolyte of 'sodium chloride or sodium sulphate of density sp. gr. 1.10 is introduced into wood vats, into which are placed iron or mild steel anodes connected to a supply of D. C. current.
The electrolyte is maintained at a temperature of 80 to 90 C., and the current density is approximately .3 amp. per square inch.
The electrolysis produces a bluish white premaximum purity, and which will be cheaper to cipitate of ferrous hydroxide of an extremely carry into effect than has been the case hitherto. tenuous nature. Owing to the exposure of the Heretofore proposals have been made for the electrolyte to the atmosphere, this precipitate in production of iron oxide for the manufacture of time would become oxidised to a black ferricpigments which have consisted in precipitating ferrous hydroxide. However to accelerate the a ferrous oxide by the chemical process of addprocess of oxidation, air is continuously blown ing hydrate of lime, carbonate of soda or the into the electrolyte. The continuous blowing of equivalent, to a solution of a ferrous salt such air into the electrolyte also results in a precipias ferrous sulphate, and oxidising the precipitate which settles easily and more readily'sepatated ferrous oxide by blowing air into the solurates from the electrolyte by filtration in a filter tion containing the precipitate to convert the press. The black hydroxide is washed with water ferrous to ferric oxide. In another proposal, the in a filter press, dried in a hot air oven at 100 ferrous oxide was precipitated electrolytically, C., and subsequently ground to the requisite fineremoved from the electrolytic bath, washed and ness in a suitable mill. dried, and then roasted to produce ferric oxide. The product after drying is a black hydroxide According to another electrolytic process, the of iron, stable at 100 C. solutions produced at the respective electrodes To produce th r 0 101115 of oxid from brown were each led away in separate streams and subt deep r d, the black hydroxide is calcined in q n y brought together Outside the electrolya suitable furnace with excess air, the degree of sis cell to precipitate the ferrous oxide which temperature affecting the resulting colour. For was Subsequently oxidised mother liquor. example at 2Q0 C. a brown is obtained I have found that by Producing the iron oxide at 600 0. a bright Turkey red is obtained, at electrolytically, a finer quality of pigment is ob- 00 a, deep Turkey red and at 10000 an tained than with chemical methods, and accorddian red pigment is produced. ing to the present invention the electrolytic me In drder to produce a maroon or ochre like eipiieiion 9 the 'PP hydroxlde 1S cqmbmed pigment, in an alternative process the paste from the -o of the made the filter press is mixed with water to form a ciplta'Ped Whlle Stm m suspanslol} m the 6180' slurry. To the slurry is added an oxidizing agent, trolytic bath to produce a ferric-ferrous hypreferably a solution of sodium hypocmorite dmxide' m f t 4 which oxidizing agent is preferably made by In.add1t1n to the Q 0 plgmen 0 electrolysis of sodium chloride. The whole mixobtamed by electrolytic precipitation of the iron ture is then boiled until a ferric hydroxide of oxide as above mentioned, the process according niform 1i ht brown c010 is btained F to the invention reduces the number of reagents :ulnh o epmus ate is then added and the boiling continued employed to a minimum, and, with the oonvenm f h d hr t k ience'of cheap electric power for the electrolytic 1 3 ,5 g e plgmen nown as precipitation, enables the complete process to be em 8 OW 1s orme carried out in one industrial-as distinct from The Plgment separated y means Of a filter chemicaloperation, and so gives an improved g g: Ki ali wlth water and the Paste dned n 1 nt by means of a cheap and co Ven e If desired air may lie blown through in addi- In order t obtain maximmn purity the l tion the step of adding the oxidizing agent. trolysis current is preferably reversed at inter- It 15 Important that the oxidizing ent be vals of about 30 minutes. Otherwise there is a introduced apart m t e ct o te. tendency for metallic iron coming down as black By calcining with excess of air as mentioned specks in connection with the first process a similar range of shades from light maroon or ochre to dark maroon may be obtained.
According to one example of the above alternative process, an electrolysis vat containing sodium chloride is connected in closed circuit with the mixing vat. Sodium hypochlorite from the electrolysis vat is admitted to the mixing vat and at the same time the mixture in the mixing vat is subjected to boiling. Sodium hypochlorite is continued to be admitted to the mixing vat until the required amount of oxidation has taken place as a result of the combined action of the 7 liquor in the mixing vat--which is sodium chloride,is pumped back to the electrolysis vat.
Ferric sulphate is now added to the paste in the mixing vat and boiling is continued until the ferric hydroxide ochre or ferrite pigment is obtained.
The pigment is then transferred to a second filter press, separated and washed anddried, and if desired calcined to temperatures depending on the depth of colour required.
By the process according to the invention iron oxide pigment from black to deep reds, maroons or ochres of a purity of 99.5% is obtained.
I claim:
1. The process for producing maroon or ochre like pigments, comprising precipitating ferrous hydroxide by the electrolysis with iron electrodes of a solution of an ionizable alkali metal salt, and oxidising the ferrous hydroxide precipitated while in suspension in the electrolysis bath to produce a ferric ferrous hydroxide, washing with water the ferric ferrous hydroxide, separating the said hydroxide, mixing the hydroxide. with water to form a slurry, adding an oxidising agent to said slurry, boiling the mixture until a ferric hydroxide of uniform light brown colour is obtained, then adding ferrous sulphate and continuing boiling until a ferric hydroxide ochre pigment known as ferrite is obtained.
2. The process for producing maroon or ochre like pigments, comprising precipitating ferrous hydroxide by the electrolysis with iron electrodes of a solution of an ionizable alkali metal salt, and oxidising the ferrous hydroxide precipitated while in suspension in the electrolysis bath to produce a ferric ferrous hydroxide, washing with water the ferric ferrous hydroxide, separating the said hydroxide, mixing the hydroxide with water to form a slurry.'adding sodium hypochlorite to said slurry, boiling the mixture until a uniform light brown colour is obtained, then adding ferrous sulphate and continuing boiling until a ferric hydroxide ochre pigment known as ferrite is obtained.
3. The process for producing maroon or ochre like pigments, comprising precipitating ferrous hydroxide by the electrolysis with iron electrodes of a solution of an ionizable alkali metal salt, and oxidising the ferrous hydroxide precipitated while in suspension in the electrolysis bath to produce a ferric ferrous hydroxide, washing with water the ferric ferrous hydroxide, separating the said hydroxide, mixing the hydroxide with water to form a slurry, adding to said slurry sodium hypochlorite which is obtained by the electrolysis of sodium chloride, the sodium hypochlorite giving up its oxygen during the first boiling and the resulting restored sodium chloride being used again in the electrolysis process for producing the sodium hypochlorite, the same sodium chloride thus being usable continually as an oxygen carrier for the oxidation step, boiling the mixture until a uniform light brown colour is obtained, then adding ferrous sulphate and continuing boiling until a ferric hydroxide ochre pigment known as ferrite is obtained.
THOMAS GLENWRIGHT FRENCH.
US299761A 1938-09-30 1939-10-16 Process for the manufacture of iron oxide Expired - Lifetime US2289258A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2289258X 1938-09-30

Publications (1)

Publication Number Publication Date
US2289258A true US2289258A (en) 1942-07-07

Family

ID=10903123

Family Applications (1)

Application Number Title Priority Date Filing Date
US299761A Expired - Lifetime US2289258A (en) 1938-09-30 1939-10-16 Process for the manufacture of iron oxide

Country Status (1)

Country Link
US (1) US2289258A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2429209A (en) * 1944-03-28 1947-10-21 Sherwin Williams Co Manufacture of iron hydrate
US2656282A (en) * 1951-01-26 1953-10-20 Wheatland Tube Co Method for the production of iron oxide from ferrous solutions
US3073763A (en) * 1958-04-17 1963-01-15 Magneto Chemie N V Electrolytic production of mixed metal oxides
US3141835A (en) * 1960-02-05 1964-07-21 Electro Chimie Metal Method and apparatus for determining oxygen in a molten halogenated bath
US3256162A (en) * 1962-03-02 1966-06-14 Paul S Roller Method for the electrolytic production of metal hydroxides

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2429209A (en) * 1944-03-28 1947-10-21 Sherwin Williams Co Manufacture of iron hydrate
US2656282A (en) * 1951-01-26 1953-10-20 Wheatland Tube Co Method for the production of iron oxide from ferrous solutions
US3073763A (en) * 1958-04-17 1963-01-15 Magneto Chemie N V Electrolytic production of mixed metal oxides
US3141835A (en) * 1960-02-05 1964-07-21 Electro Chimie Metal Method and apparatus for determining oxygen in a molten halogenated bath
US3256162A (en) * 1962-03-02 1966-06-14 Paul S Roller Method for the electrolytic production of metal hydroxides

Similar Documents

Publication Publication Date Title
US2289258A (en) Process for the manufacture of iron oxide
US3619137A (en) Production of iron oxide pigments
CN103896325A (en) Calcined zinc oxide production technology
US2620261A (en) Method of making iron oxide pigment
CN111039495A (en) Comprehensive recovery method of waste rare earth polishing powder and steel pickling waste liquid
US1412174A (en) Art of making electrolytic iron
US3869359A (en) Method of making intimately admixed metal oxides
US1840326A (en) Production of yellow iron oxide pigments
US2226573A (en) Process of making cadmium red pigment
US1333849A (en) Solution of titanium and iron salts and the process of preparing same
US2716595A (en) Manufacture of red hydrous ferric oxide
US1596363A (en) Manufacture of oxide pigments
US1337402A (en) Manufacture of pure ferric oxid
US2288503A (en) Electrolytic basic metal chromate pigment manufacture
US1392926A (en) Pigment and method of producing the same
Bruckner The Electrolytic Production of Turkey Red Iron Oxide Pigment
US2090476A (en) Pigment and methods of preparing the same
US1496605A (en) Process for producing ferric pigments
US2416551A (en) Production of chromium compounds
US292753A (en) Johaknt kael kesslee
US2173895A (en) Process for producing sulphide pigments
US2633407A (en) Process for producing red unhydrated iron oxide
US2237311A (en) Preparation of cadmium pigments
US1412027A (en) Titanium-oxide pigment and method of producing the same
US2023928A (en) Chrome yellow color