US1084856A - Method of manufacturing phosphoric acid. - Google Patents
Method of manufacturing phosphoric acid. Download PDFInfo
- Publication number
- US1084856A US1084856A US79212113A US1913792121A US1084856A US 1084856 A US1084856 A US 1084856A US 79212113 A US79212113 A US 79212113A US 1913792121 A US1913792121 A US 1913792121A US 1084856 A US1084856 A US 1084856A
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- US
- United States
- Prior art keywords
- phosphoric acid
- furnace
- bath
- manufacturing phosphoric
- manufacturing
- 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
Links
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 title description 15
- 229910000147 aluminium phosphate Inorganic materials 0.000 title description 7
- 238000004519 manufacturing process Methods 0.000 title description 6
- 239000000463 material Substances 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000378 calcium silicate Substances 0.000 description 3
- 229910052918 calcium silicate Inorganic materials 0.000 description 3
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000002893 slag Substances 0.000 description 3
- 150000001721 carbon Chemical class 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 208000020673 hypertrichosis-acromegaloid facial appearance syndrome Diseases 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- 239000002367 phosphate rock Substances 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B25/00—Phosphorus; Compounds thereof
- C01B25/16—Oxyacids of phosphorus; Salts thereof
- C01B25/18—Phosphoric acid
- C01B25/20—Preparation from elemental phosphorus or phosphoric anhydride
Definitions
- This invention relates to an improvement in the method of manufacturing phosphoric acid by heating silicious material with phosphatic material and the object of the invention is to overcome the difficulty presented by the formation of a high resistance-glass slag in the furnace.
- this carbon should act as a reducing agent, but inasmuch as a certain amount of the phosphoric acid liberated from the calcium silicate may be reduced by the carbon, it is desirable tointroduce or mix air with the furnace gases as they are withdrawn to thereby reoxidize any reduced oxids.
- My invention may be practised in connection with any suitable or well known form of electric resistance furnace with either double or 'singlearcs, and for the sake of illustrationI have shown in v the accompanying drawing an electric resistance furnace having two electrodes, the current passing from one electrode to the fused bath and thence to the other electrode.
- the process could be equally well practised, however, with a furnace in which the crucible was one terminal and a single electrode the other.
- Figure 1 represents a longitudinal vertical section through a furnace in which the method may be car'- ried out.
- Fig. 2 is a cross section, and Fig. 3 1s a sectional plan View.
- A represents the furnace chamber built with suitable walls of tire brick or other refractory material in accordance with the usual practice.
- B and O represent the electrodes of carbon or graphite extending in an inclined direction through the end walls and adapted to produce arcs against the surface of the molten bath 10 which will be formed in the furnace soon after starting thereof, the molten material being in normal operation tapped out from time to time through tap holes 11 and 12 which are normally closed by plugs 13 and 14:.
- the mixture to be furnaced which may consist of natural phosphate rock and silica, is fed into the furnace at the sides of the electrodes through suitable hoppers D and E, the material forming piles 15 and 16 on the bottom of the furnace and at the sides of the electrodes, the material in the center being melted to form a molten bath by the action of the electric current.
- the path of the current is thus longitudinally from one end to the other of the bath, and as stated previously the high resistance of the calcium silicate slag will make it diflicult to maintain the continuity and uniformity of the current flow.
- this difficulty is overcome by introducing broken carbon from time to time through a suitable hopper F between the electrodes, this carbon forming a conducting path 17 of relatively higher current density on the surface of the molten bath and between the electrodes.
- the amount of carbon introduced will be regulated to correspondwith the current required and thus provides a drawn in through the feed openings. If desired, separate inlets may be provided for the air.
- the step in the process of manufacturing phosphoric acid by heating phosphatic material with silicious material in the electric furnace which comprises producing and maintaining a conducting path of increased current density in the furnace by adding to the bath a material having a higher conductivity than the bath.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Glass Compositions (AREA)
Description
M. M. HAPP.
METHOD OF MANUFACTURING PHOSPHORIC ACID.
APPLICATION FILED SEPT. 27, 1913.
1 ,O84,856, Patented Jan. 20, 1914.
UNITE STATES PATENT OFFICE.
MAXIMILIAN MATTI-IEUS HAFF, OF OTTAWA, ONTARIO, CANADA, ASSIGNOB TO THOMAS LEOPOLD WILLSON OF OTTAWA, ONTARIO, CANADA.
METHOD OF MANUFACTURING PHOSPHOR-IC ACID.
Specification of Letters Patent.
Patented Jan. 20, 1914.
Applicatiorifiled September 27, 1913. Serial No. 792,121.
To all whom it may concern:
Be it known that I, MAXIMILIAN MAT- TIIEUs HAFF, a subject of the King of Great Britain, residing at 188 Metcalfe street, city of Ottawa, county of Carleton, Province of Ontario, Dominion of Canada, have invented certain new and useful Improvements in Methods of Manufacturing Phosphoric Acid, of which the following is a specification.
This inventionrelates to an improvement in the method of manufacturing phosphoric acid by heating silicious material with phosphatic material and the object of the invention is to overcome the difficulty presented by the formation of a high resistance-glass slag in the furnace.
To expel phosphoric acid by electrically heating a mixture of phosphatic material such as calcium phosphate with silicious material such as silica,,it is necessary that a higher temperature than that of mere fusion be produced, and it is extremely difficult to pass suflicient current through the bath to produce this temperature, owing to the high resistance of t e calcium silicate slag. I have found that if a path of increased current density be formed in the furnace, as by introducing broken carbon to the surface of the bath, between the electrodes, this difficulty is overcome. It is not intended that this carbon should act as a reducing agent, but inasmuch as a certain amount of the phosphoric acid liberated from the calcium silicate may be reduced by the carbon, it is desirable tointroduce or mix air with the furnace gases as they are withdrawn to thereby reoxidize any reduced oxids.
My invention may be practised in connection with any suitable or well known form of electric resistance furnace with either double or 'singlearcs, and for the sake of illustrationI have shown in v the accompanying drawing an electric resistance furnace having two electrodes, the current passing from one electrode to the fused bath and thence to the other electrode. The process could be equally well practised, however, with a furnace in which the crucible was one terminal and a single electrode the other.
Referring to the drawing, Figure 1 represents a longitudinal vertical section through a furnace in which the method may be car'- ried out. Fig. 2 is a cross section, and Fig. 3 1s a sectional plan View.
Referring to the drawing, A represents the furnace chamber built with suitable walls of tire brick or other refractory material in accordance with the usual practice.
B and O represent the electrodes of carbon or graphite extending in an inclined direction through the end walls and adapted to produce arcs against the surface of the molten bath 10 which will be formed in the furnace soon after starting thereof, the molten material being in normal operation tapped out from time to time through tap holes 11 and 12 which are normally closed by plugs 13 and 14:.
The mixture to be furnaced, which may consist of natural phosphate rock and silica, is fed into the furnace at the sides of the electrodes through suitable hoppers D and E, the material forming piles 15 and 16 on the bottom of the furnace and at the sides of the electrodes, the material in the center being melted to form a molten bath by the action of the electric current. The path of the current is thus longitudinally from one end to the other of the bath, and as stated previously the high resistance of the calcium silicate slag will make it diflicult to maintain the continuity and uniformity of the current flow. In accordance with the present invention this difficulty is overcome by introducing broken carbon from time to time through a suitable hopper F between the electrodes, this carbon forming a conducting path 17 of relatively higher current density on the surface of the molten bath and between the electrodes. The amount of carbon introduced will be regulated to correspondwith the current required and thus provides a drawn in through the feed openings. If desired, separate inlets may be provided for the air.
What I claim as my invention is:
1. The steps in the process of manufacturing phosphoric acid by heating ph0sphatic material with silici-ous material in the electric furnace which comprises fusing the charge placing broken carbon on the bath to form a conducting path of increased current density and mixing air with the furnace gases to reoxidize any reduced phosphorous oxids.
2. The step in the process of manufacturing phosphoric acid by heating phosphatic material with silicious material in the electric furnace, which comprises producing and maintaining a conducting path of increased current density in the furnace by adding to the bath a material having a higher conductivity than the bath.
In witness whereof I have hereunto set my hand in the presence of two witnesses.
MAXIMILIAN MATTHEUS HAFF.
Witnesses RUssEL S. SWART, PEARL M. GARRAW.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79212113A US1084856A (en) | 1913-09-27 | 1913-09-27 | Method of manufacturing phosphoric acid. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79212113A US1084856A (en) | 1913-09-27 | 1913-09-27 | Method of manufacturing phosphoric acid. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1084856A true US1084856A (en) | 1914-01-20 |
Family
ID=3153083
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US79212113A Expired - Lifetime US1084856A (en) | 1913-09-27 | 1913-09-27 | Method of manufacturing phosphoric acid. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1084856A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2531612A (en) * | 1944-02-10 | 1950-11-28 | Saint Gobain | Method for melting glass by electricity |
-
1913
- 1913-09-27 US US79212113A patent/US1084856A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2531612A (en) * | 1944-02-10 | 1950-11-28 | Saint Gobain | Method for melting glass by electricity |
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