US588266A - Guillaume de chalmot - Google Patents
Guillaume de chalmot Download PDFInfo
- Publication number
- US588266A US588266A US588266DA US588266A US 588266 A US588266 A US 588266A US 588266D A US588266D A US 588266DA US 588266 A US588266 A US 588266A
- Authority
- US
- United States
- Prior art keywords
- phosphate
- furnace
- phosphoric acid
- molten
- sand
- 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
- 229910019142 PO4 Inorganic materials 0.000 description 42
- 235000021317 phosphate Nutrition 0.000 description 40
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 36
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 36
- 239000010452 phosphate Substances 0.000 description 36
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 26
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 18
- 239000004576 sand Substances 0.000 description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 8
- 239000002367 phosphate rock Substances 0.000 description 8
- 239000000377 silicon dioxide Substances 0.000 description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical compound [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 239000011435 rock Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- PGYDGBCATBINCB-UHFFFAOYSA-N 4-diethoxyphosphoryl-n,n-dimethylaniline Chemical compound CCOP(=O)(OCC)C1=CC=C(N(C)C)C=C1 PGYDGBCATBINCB-UHFFFAOYSA-N 0.000 description 1
- 239000006009 Calcium phosphide Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05B—PHOSPHATIC FERTILISERS
- C05B13/00—Fertilisers produced by pyrogenic processes from phosphatic materials
- C05B13/02—Fertilisers produced by pyrogenic processes from phosphatic materials from rock phosphates
Definitions
- Thisinvent-ion relates to an improved treat- .ment of phosphates, and especially natural phosphates or phosphate-rocks, the purpose of which is to render the phosphoric acid contained in them more soluble and available as plant-food.
- an electric furnace comprising a hollow hearth having a bottom of carbon or other conducting material connected with one electrode and a pencil or pencils of carbon arranged 5 above the hearth and connected with the opposite electrode or terminal of a suitable dynamo or (in case of alternatingcurrents) with the opposite terminals of a transformer.
- phosphate-rock broken into lumps of suit- 50 able size, is placed in the furnace, and an arc is started by which the phosphate is fused and accumulates in a pool on the hearth, more phosphate-rockbeing added until after a time the molten phosphate stands high enough in the furnace to run over the wall'of the hearth on one side.
- Fresh rock is fed into the furnace as fast as it becomes molten and consequently the molten phosphate continues torun over and flow out immediately.
- the red notion of the phosphoric acid is almost wholly prevented. Only that portion of the molten phosphate which is at the bottom of the pool becomes reduced, and this portion remains in the furnace.
- the molten phosphate which overflows from the furnace is caused to fall immediately onto sand, and more sand is sprinkled over it.
- the partial reaction which thus occurs increases the proportion of soluble phosphoric acid.
- the phosphate while very hot is then-dumped into Water, which causes it to crack in all di rections, so that it can easily be crushed. After cooling, the phosphate has only to be finely crushed or reduced to a fine powder to be immediately available as a fertilizer.
- Figure 1 is a vertical section
- Fig. 2 is a vertical transverse section cut on the line 2 2 in Fig. 1.
- a designate the carbon pencil or electrode'of the furnace which is built up usually of slabs of carbon carried bya suit-able head or holder and adjustable vertically, and b the hearth or crucible. or cavity of the furnace, which has a bottom layer of carbon superposed, preferably, upon a plate of iron connected by copper cables 0 to one terminal of the dynamo or transformer, while the holder for the carbon pencil is connected to the opposite terminal.
- the furnace- is constructed with a Wall d on one side somewhat lower than the other walls and arranged to slope outwardly to facilitate the overflowing of the molten phosphate.
- the phosphate which flows over this wall falls on to a slowly-revolv ing iron cylinder a, mounted beneath the furnace and rotated by any suitable means.
- a hopper or chute h from which sand is discharged upon the cylinder, falling sufiiciently to one side, as shown in Fig. :2, to strike the cylinder before the phosphate can fall upon it, in order to cover its surface with a layer of sand and prevent as far as possible direct contact of the hot phosphate with the iron of the cylinder.
- the cylinder is protected by the sand from the heat of the phosphate, and being hollow it is able to rapidly cool on all sides by radiation, or it may be cooled by a current of water, as by playing a hose upon it or running water into it.
- Beneath the cylinder is arranged a water-tank f, 1nto which as the cylinder slowly revolves the phosphate is caused to drop;
- the phosphate-rock falls in to the water it cracks in all directions, so that it can afterward easily be reduced to a fine power.
- the tank which is mounted on trunnions, is turned over, so as to dump out the phosphate, which falls on a sieve or grating g.
- the phosphate remains on the grating and the water flows off.
- the wall (1 of the furnace is made best of phosphate-rock and can at any time be easily replaced.
- the bottom of the furnace-hearth remains always covered with liquid phosphate which cannot run 0E. This is-of great practical advantage, because the phosphate" becomes reduced where it touches the carbon bottom, and calcium phosphide is formed, which is not a plant-food, but, on the contrary, is somewhat poisonous.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Vertical, Hearth, Or Arc Furnaces (AREA)
Description
(No Model.)
G. DE GHALMOT.- TREATMENT OF PHOSPHATES.
No. 588,266. v Pa .tented Aug.17,1897.
WITNESSES: INVENTOR: I
fi /Z M By his Attorneys,
W 6am g UNITED STATES GUILLA UME DE OHALMOT, OF LEAKSVl-LLE, NORTH CAROLINA, ASSIGNOR TO THE VVILLSON LABORATORY COMPANY, OF NEYV YORK, N. Y.
TREATMENT OF PHOISPHATES.
SPECIFICATION forming part of Letters Patent No. 588,266, dated August 17, 1897. Application filed December 20, 1895. Serial No. 572,733. specimens.)
1'0 all whom it nuu concern.-
Be it known that I, GUILL-AUME DE CHAL- MOT, a subject of the Queen of the Netherlands, (having declared my intention of be- 5 coming a citizen of the United States,) residiug in Leaksville, in the county of Rockingham and State of North Carolina, have invented'certain new and useful Improvements in the Trea ment 'of Phosphates, of which the following is a specification.
Thisinvent-ion relates to an improved treat- .ment of phosphates, and especially natural phosphates or phosphate-rocks, the purpose of which is to render the phosphoric acid contained in them more soluble and available as plant-food.
I have discovered that if natural phosphates are molten in an electric furnace the phosphoric acid contained in them becomes more soluble. I have also found that the phosphate should not remain in the furnace after it is fused, but should be removed as quickly as possible, as otherwise the amount of available phosphoric acid decreases by a part of the phosphoric acid becoming reduced or volatilized. I have also found that if the molten phosphate is run into and mixed with sand this treatment renders the phosphoric acid still more soluble.
I have practiced my invention with a red phosphate-rock containing twenty-three per cent. of phosphoric acid, but almost worthless for fertilizing purposes, since only 1.39 per cent. of the phosphoric acid is soluble in 3 5 Wagners citrate solution. After treatment according to my invention, even without mixing with sand, thewsulting phosphate contains 29.50 per cent. phosphoric acid, of which 9.5 per cent. is soluble in the citrate solution.
In practicing my invention I employ an electric furnace comprising a hollow hearth having a bottom of carbon or other conducting material connected with one electrode and a pencil or pencils of carbon arranged 5 above the hearth and connected with the opposite electrode or terminal of a suitable dynamo or (in case of alternatingcurrents) with the opposite terminals of a transformer. The
phosphate-rock, broken into lumps of suit- 50 able size, is placed in the furnace, and an arc is started by which the phosphate is fused and accumulates in a pool on the hearth, more phosphate-rockbeing added until after a time the molten phosphate stands high enough in the furnace to run over the wall'of the hearth on one side. Fresh rock is fed into the furnace as fast as it becomes molten and consequently the molten phosphate continues torun over and flow out immediately. By this means the red notion of the phosphoric acid is almost wholly prevented. Only that portion of the molten phosphate which is at the bottom of the pool becomes reduced, and this portion remains in the furnace. The molten phosphate which overflows from the furnace is caused to fall immediately onto sand, and more sand is sprinkled over it. The partial reaction which thus occurs increases the proportion of soluble phosphoric acid. The phosphate while very hot is then-dumped into Water, which causes it to crack in all di rections, so that it can easily be crushed. After cooling, the phosphate has only to be finely crushed or reduced to a fine powder to be immediately available as a fertilizer.
The accompanying drawings illustrate the construction of furnace and accessory apparatus suitable for practicing my invention.
Figure 1 is a vertical section, and Fig. 2 is a vertical transverse section cut on the line 2 2 in Fig. 1.
Let a designate the carbon pencil or electrode'of the furnace, which is built up usually of slabs of carbon carried bya suit-able head or holder and adjustable vertically, and b the hearth or crucible. or cavity of the furnace, which has a bottom layer of carbon superposed, preferably, upon a plate of iron connected by copper cables 0 to one terminal of the dynamo or transformer, while the holder for the carbon pencil is connected to the opposite terminal. The furnace-is constructed with a Wall d on one side somewhat lower than the other walls and arranged to slope outwardly to facilitate the overflowing of the molten phosphate. The phosphate which flows over this wall falls on to a slowly-revolv ing iron cylinder a, mounted beneath the furnace and rotated by any suitable means. Above this cylinder is arranged a hopper or chute h, from which sand is discharged upon the cylinder, falling sufiiciently to one side, as shown in Fig. :2, to strike the cylinder before the phosphate can fall upon it, in order to cover its surface with a layer of sand and prevent as far as possible direct contact of the hot phosphate with the iron of the cylinder. Some of the sand, however, falls upon the phosphate, so that the latter is thus brought thoroughly into contact with the sand both above and below. The cylinder is protected by the sand from the heat of the phosphate, and being hollow it is able to rapidly cool on all sides by radiation, or it may be cooled by a current of water, as by playing a hose upon it or running water into it. Beneath the cylinder is arranged a water-tank f, 1nto which as the cylinder slowly revolves the phosphate is caused to drop; As the phosphate-rock falls in to the water it cracks in all directions, so that it can afterward easily be reduced to a fine power. When most of the water in the tank has evaporated, the tank, which is mounted on trunnions, is turned over, so as to dump out the phosphate, which falls on a sieve or grating g. The phosphate remains on the grating and the water flows off.
The wall (1 of the furnace is made best of phosphate-rock and can at any time be easily replaced. The bottom of the furnace-hearth remains always covered with liquid phosphate which cannot run 0E. This is-of great practical advantage, because the phosphate" becomes reduced where it touches the carbon bottom, and calcium phosphide is formed, which is not a plant-food, but, on the contrary, is somewhat poisonous. By making the bottom of the furnace of molten phosphate the reduction of the phosphate that runs over is greatly diminished.
I have employed by preference an alternating electric current whereby electrolytic action is avoided, but my invention may nevertheless be practiced with a continuous curren The action of my process in increasing the solubility of the phosphoric acid may be due partly to the formation of silico-phosphate of lime according to the equation ca,r,o,+sio,+2oaoo,=5oao,P,o,,sio,+2co,.
In these reactions Fe or Al may replace (3a. In this equation both SiO and (laCO are supposed to prexist in the phosphate, winch is generally the case. The rock which i have used contained 3.22 per cent. of SiO,; or it is possible that a part of the iron oxid and alumina is disunited from the phosphoric acid by the high heat; or it is possibio and even likely that other reactions are lnvolved the nature of which is as yet not known. The fact that phosphate containing only as little silica as 3.22 per cent. can be made soluble by my process points in this direction.
I do not claim in this application the electric fusing of a mixture of phosphate-rock and sand or silica, as I have made another mvention involving that process, which is made the subject of a separate application for patent, filed December 21, 1895, Serial No. 572,842.
I am aware that phosphates have been heated with carbon in an electric furnace to drive off and reduce the phosphoric acid to produce phosphorus, but this is a difierent process from my invention. I employ no reducing agent and aim not to drive oif the phosphoric acid and not to reduce it, nor do I employ any iluxing materials which would promote the liberation of phosphoric 'acid,but, on the contrary, avoid their use. In fact the opposite expedient of adding lime, which would prevent loss of phosphoric acid, would be within the practical application of my invention. I resort, therefore, to the simple fusion of the phosphate at a high temperature without the addition of either a reducing agent or a flux, and by this process produce -before specified, namely:
1. The treatment of natural phosphate-rock containingsilica,alumina,oriron oxid by simpie fusionin anelectric furnace, whereby the proportion of soluble phosphoric acid is increased, and immediately removing the molten phosphate from the furnace, whereby its reduction is prevented.
2. The treatment of natural pl'iosphate-rock containing silica, alumina, or iron oxid, by fusion in an electric furnace, whereby the proportion of soluble phosphoric acid is increased, removing the molten phosphate from the furnace, and bringing it into contact with silica,whereby the phosphoric acid is rendered still more soluble.
3. The treatment of natural phosphate-rock containing silica, alumina, or iron oxid, by simple fusion in an electric furnace, without the addition of a red ueing agent, and causing the molten phosphate to overflow at the top, whereby the reduction of the phosphate which is thus discharged is prevented, the reduced phosphate which is confined to the bottom of the molten mass being retained in the 1' urnacc.
4. The treatment of phosphate by fusing it in an electric furnace, and causing the molten phosphate to overflow from the top of the f urnacc, dropping it onto silica, and sprinkling silica over it.
5. The treatment of phosphate by fusing it in an electric furnace, removing the molten phosphate from the furnace and bringing it into contact with silica, and then while still hot dropping it into waterl In witness whereof I have hereunto signed my name in the presence of two subscribing witnesses.
G. DE OIIALMOT.
\Vitnesses:
J. M. HOPPER,
P. JARRETT.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US588266A true US588266A (en) | 1897-08-17 |
Family
ID=2656932
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US588266D Expired - Lifetime US588266A (en) | Guillaume de chalmot |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US588266A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE750708C (en) * | 1935-09-24 | 1945-01-25 | Union Fabrik Chemischer Produc | Process for the production of a melt phosphate containing free colloidal silica |
-
0
- US US588266D patent/US588266A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE750708C (en) * | 1935-09-24 | 1945-01-25 | Union Fabrik Chemischer Produc | Process for the production of a melt phosphate containing free colloidal silica |
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