US502424A - Heinrich precht - Google Patents

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US502424A
US502424A US502424DA US502424A US 502424 A US502424 A US 502424A US 502424D A US502424D A US 502424DA US 502424 A US502424 A US 502424A
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potassium
phosphate
soluble
meta
precht
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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B25/00Phosphorus; Compounds thereof
    • C01B25/16Oxyacids of phosphorus; Salts thereof
    • C01B25/26Phosphates
    • C01B25/38Condensed phosphates
    • C01B25/44Metaphosphates
    • C01B25/445Metaphosphates of alkali metals

Definitions

  • My invention relates to the production of phosphate of potassium and of aluminum.
  • the meta phosphate of potassium heretofore produced is insoluble in water or substantially so, and my invention has for its obj ectaprocess whereby phosphates of potassium and of aluminum readily, in fact, completely soluble in water may be readily obtained by conversion of the insoluble into soluble salts, in which all of the contained phosphoric acid is in a form readily soluble in water;
  • This I attain as hereinafter more specifically described by subjecting the potassium meta phosphate to a melting process, and if this process is carried out in such manner that the meta phosphate is rapidly cooled, that is to say in such a manner as to prevent crystallization, an amorphous potassium salt of the concentrated metaphosphate that is readily soluble is obtained.
  • the potassium meta-phosphate may be obtained in any well-known manner, as for instance by heatingpotassium mono-phosphate (KH,PO,), or by melting, preferably by means of steam, potassium carbonate or potassium chlorid together with metaphosphoric acid in such proportions that the compound will contain one atom of I for each atom of K.
  • the melting of the insoluble potassium metaphosphate can be effected with the best advantage in a reverberatory furnace in which the phosphate is heated to such a degree as to render it fluid so that it may be allowed to flow out of a tap-hole. If the melting is effected in a reverberatory furnace provided with an inclined sole or hearth the operation can be made a continuous one by feeding the phosphate into the furnace at the highest and coolest point of the hearth, which should incline toward the source of heat, and allowing the molten material to flow from a tap-hole at the lowest and hottest point of such hearth, and if necessary the material may be raked down the incline so that the salt will be gradually reduced to a fluid state.
  • the melting of the phosphate is advantageously eifected by subjecting it to the action of an oxidizing flame as a reducing flame might result in a reduction of the phosphoric acid, which would be detrimental.
  • potassium metaphosphate that is completely soluble in water is readily obtained, as above described.
  • a basic body such as potash or soda, the quantity of which will correspond to the desired combination or composition, is added to the potassium metaphosphate either before or during the melting of the same.
  • the soluble potassium phosphates obtained as above described can be employed in the production of soluble phosphate of alumina or of orthophosphate of potassium soluble in.
  • the phosphate of alumina is mixed with the soluble potassium metaphosphate or potassium pyrophosphate or both, obtained as hereinbefore set forth, in any desired proportion within the limit of forty per cent. of phosphate of alumina, the solublepotassium meta or pyro phosphate forming with the phosphate of alumina combinations that are soluble in water and whose solutions do not decompose.
  • the phosphate of alumina is added to the potassium meta or pyrophosphate or to a mixture of them, either during the process of melting or to the potassium phosphates in the phosphoric acid solution employed as a starting material, in 1 that a'solution of phosphoric acid contaminated with or rendered impure by alu minais employed in the production of the insoluble phosphates. Should the phosphate of alumina contain a small proportion of iron the latter is also converted into a soluble form.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Compositions Of Oxide Ceramics (AREA)

Description

UNITE STATES PATE T OFFICE HEINRICH PRECHT, or NEU-sTAssFUR GERMANY,
PROCESS OF OBTAINING META OR PYRO PHOSPHORlC -ACID COMBINATIONS.
SPECIFICATION forming part of Letters Patent No. 502,424, dated August 1, 1893. Application filed June 16, 1892. Serial No. 436,945. (No specimens) To all whom it may concern:
Be it known that I, I-IEINRIOHPREOHT, a subject of the King of Prussia, residing at Ne u- Stassfurt, Prussia, Germany, have invented certain new and useful Improvements in and Relating to the Production of Phosphate of Potassium and of Alumina; and I do hereby declare the following to be a full, clear, and exact description of the invention, such as will enable others skilled in the art to which it appertains to make and use the same.
My invention relates to the production of phosphate of potassium and of aluminum.
It is well known that the meta phosphate of potassium heretofore produced is insoluble in water or substantially so, and my invention has for its obj ectaprocess whereby phosphates of potassium and of aluminum readily, in fact, completely soluble in water may be readily obtained by conversion of the insoluble into soluble salts, in which all of the contained phosphoric acid is in a form readily soluble in water; This I attain as hereinafter more specifically described by subjecting the potassium meta phosphate to a melting process, and if this process is carried out in such manner that the meta phosphate is rapidly cooled, that is to say in such a manner as to prevent crystallization, an amorphous potassium salt of the concentrated metaphosphate that is readily soluble is obtained. The potassium meta-phosphate may be obtained in any well-known manner, as for instance by heatingpotassium mono-phosphate (KH,PO,), or by melting, preferably by means of steam, potassium carbonate or potassium chlorid together with metaphosphoric acid in such proportions that the compound will contain one atom of I for each atom of K.
In carrying out my invention I proceed as follows: The insoluble potassium metaphosphate is melted and then allowed to flow into a shallow fiat iron vessel orinto shallow channels for the purpose of rapidly congealing the same so that it will not crystallize but remain in an amorphous condition. A potassium salt of the concentrated metaphosphate is thus formed which by slow cooling would revert into a crystalline and insoluble compound.
The melting of the insoluble potassium metaphosphate can be effected with the best advantage in a reverberatory furnace in which the phosphate is heated to such a degree as to render it fluid so that it may be allowed to flow out of a tap-hole. If the melting is effected in a reverberatory furnace provided with an inclined sole or hearth the operation can be made a continuous one by feeding the phosphate into the furnace at the highest and coolest point of the hearth, which should incline toward the source of heat, and allowing the molten material to flow from a tap-hole at the lowest and hottest point of such hearth, and if necessary the material may be raked down the incline so that the salt will be gradually reduced to a fluid state. The melting of the phosphate is advantageously eifected by subjecting it to the action of an oxidizing flame as a reducing flame might result in a reduction of the phosphoric acid, which would be detrimental.
Practical experience has demonstrated that a potassium phosphate completely soluble in water is obtained when the molten mass contains one molecule of phosphoric acid (P 0 to one molecule of potassium oxid (K 0) or one hundred parts by Weight of anhydrous phosphoric acid, (P 0 or phosphoric acid free from water, to at least 66.2 parts by weight of potassium oxid (K 0). In practice it will, however, be found of advantage to 0perate with a larger proportion of potassium oxid (K 0) so that phosphoric acid in the form of pyrophosphate will in part be present in the molten salt. If the proportion of potassium oxid (K 0) relatively to the phos* phoric acid is such that one partof potassium pyrophosphate to four parts of potassium metaphosphate must be formed in the molten mass, potassium metaphosphate that is completely soluble in water is readily obtained, as above described. In order that these proportions may be obtained a basic body, such as potash or soda, the quantity of which will correspond to the desired combination or composition, is added to the potassium metaphosphate either before or during the melting of the same.
The soluble potassium phosphates obtained as above described can be employed in the production of soluble phosphate of alumina or of orthophosphate of potassium soluble in.
water as follows: In the production of phosphate of alumina soluble in water, the phosphate of alumina is mixed with the soluble potassium metaphosphate or potassium pyrophosphate or both, obtained as hereinbefore set forth, in any desired proportion within the limit of forty per cent. of phosphate of alumina, the solublepotassium meta or pyro phosphate forming with the phosphate of alumina combinations that are soluble in water and whose solutions do not decompose. The phosphate of alumina, as such and in its insoluble form, is added to the potassium meta or pyrophosphate or to a mixture of them, either during the process of melting or to the potassium phosphates in the phosphoric acid solution employed as a starting material, in 1 that a'solution of phosphoric acid contaminated with or rendered impure by alu minais employed in the production of the insoluble phosphates. Should the phosphate of alumina contain a small proportion of iron the latter is also converted into a soluble form.
In the production of potassium orthophos- 3 version take place, said conversion being completed in about two hours at a temperature of about 120 centigrade, the reaction being vsomewhat accelerated by addition of phos* phoric acid to the solution.
ble for use as fertilizers in that they contain potassium oxid and phosphoric acid and are therefore well adapted as substitutes for that :class of fertilizers which 'contain chemical combinations of potassium together with phosphatic constituents, and have the advantage over the latter fertilizers in that said products do not contain undesirable chlorids.
Having thus described my invention, what I claim as new therein, and desire to secure by Letters Patent, is
1. The herein-described processof obtain- 'ing meta or pyro-phosphoric acidcombina 'tions from phosphate salts of the metals of "thealkalies, which consists "inmelting the in soluble salt or salts and rapidly coolingthe same to prevent crystallization for the pur- {pose set forth. A
2; The herein described process'of' obtaining meta or pyro-phosphoric'acidcombinations, from phosphate salts of the metals of 5 the alkalies, which eonsistsin melting the insoluble salt together with a salt of the metals of the alkalies, and rapidly cooling the same to prevent crystallization for the purposeset forth.
HEINRICH PRECHT.
Witnesses:
EGGELING, E. KOHLE.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3230040A (en) * 1962-01-02 1966-01-18 Monsanto Co Trimetaphosphate processes
US3230039A (en) * 1962-01-02 1966-01-18 Monsanto Co Process for manufacturing sodium trimetaphosphate products

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3230040A (en) * 1962-01-02 1966-01-18 Monsanto Co Trimetaphosphate processes
US3230039A (en) * 1962-01-02 1966-01-18 Monsanto Co Process for manufacturing sodium trimetaphosphate products

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