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US1422699A - Process of producing phosphoric acid - Google Patents

Process of producing phosphoric acid Download PDF

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Publication number
US1422699A
US1422699A US481082A US48108221A US1422699A US 1422699 A US1422699 A US 1422699A US 481082 A US481082 A US 481082A US 48108221 A US48108221 A US 48108221A US 1422699 A US1422699 A US 1422699A
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Prior art keywords
phosphoric acid
phosphorus
expelled
forming
oxides
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US481082A
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Ernest W Guernsey
Yee Jew Yam
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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
    • C01B25/18Phosphoric acid
    • C01B25/20Preparation from elemental phosphorus or phosphoric anhydride

Definitions

  • PROCESS OF PRODUCING PHOSPHORIG ACID PROCESS OF PRODUCING PHOSPHORIG ACID.
  • the subject ofthis invention is a process of producing phosphoric acid.
  • he main object of the invention is the provision of a process for liberating phosphoric acid from natural and artificial phosphates of the metals by means of silica and carbon at temperatures below fusion and in a more simple and economical manner than has heretofore been possible.
  • Our invention may be carried out in any apparatus in which solidmaterial may be convenientl handled and efliciently heated to l300 under conditions sufiiciently non-oxidizing to prevent the burning of the carbon in the charge before it can perform its function of reducing calcium phosphate.
  • silica, SiO are-in the molecular ratio of- 1:1 and carbon is present in at least 50% excess-of that required by the equation
  • the actual proportions of phosphate rock, sand and coal will vary according to the composition of these materials as will be understood by thoseskilled in the art.
  • This claim and desire to secure by mixed charge is preferably formed into briquettes according to known methods, and is then fed into an internally fired kiln in which the fuel and air are so proportioned that a reducing or at least not-strongly oxidizing atmosphere is maintained. The heat is so regulated that the charge is brought only to incipient clinkering orslightly under. Under these conditions practically all of the phosphorus is evolved 111 the elementary state.
  • the duration of the heating necessary to secure complete expulsion of the P 0 depends on the fineness and intimacy of mixing of the materials on the physical structure of the phosphate rock, on the exact composition of the charge, etc. For an ordinary Florida or Tennessee phosphate rock the time of heating need not exceed one hour at the most if the materials are ground to a fineness under 100 mesh.
  • the ases from the kiln, containing the expelle phosphorus may be burned under boilers or other heat conserving devices.
  • the oxides of phosphorus contained in the gases from the burners may be collected in any suitable manner as for instance by a Cottrell precipitator or they may be absorbed in any well known and usual manner.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Silicates, Zeolites, And Molecular Sieves (AREA)

Description

UNHT stares ERNEST W. GUERNSEY J'EW YAM YEE, OF WASHINGTON, DISTRICT OF COLUMBIA.
Parana oral ca.
PROCESS OF PRODUCING PHOSPHORIG ACID.
No Drawing. Application filed June 28,
To all whom it may concern:
Be it known that we, ERNEST VVfGoER SEY and JEW YAM YEE, citizens of the United States, and residents of Washington, District of Columbia, have invented an Improvement in Processes of Producing Phosphoric Acid, of which the following is a specification.
The subject ofthis invention is a process of producing phosphoric acid.
he main object of the invention is the provision of a process for liberating phosphoric acid from natural and artificial phosphates of the metals by means of silica and carbon at temperatures below fusion and in a more simple and economical manner than has heretofore been possible.
In order that our invention maybe more clearly understood, and that it may be more easily differentiated from the prior art the following facts are submitted.
It is Well known that phosphorus can be practically completely expelled by intense heating of a properly proportioned mixture of 'phosphatic material, sand and car-' bonaceous material. The reaction which takes place may be summarized by the equation:
It has enerally been believed that a practical lifieration of P 0 by this reaction could be obtained only at the temperature at which a fluid melt is obtained. This temperature can be easily attained only in electric furnaces. As is. well known, the use of electric current for melting purposes is very expensive. In fact, we have made a calculation on the cost of phosphoric acid produced in this way and have found that with electric power at $.005 per K. W. H.'the cost of electricity for heating is more than 50% of the total cost of the phosphoric acid produced. A further disadvantage and expense connected with the use of an electric furnace is the lining replacement charges due to high temperatures employed. Moreover, a relatively large amount of high grade labor is required to operate an electric furnace. Finally, an, expensive and complicated auxiliary electrical installation is required.
We have made a large number of experiments and have confirmed the general belief that a practical liberation of P 0 can Specification of Letters Patent.
. ments.
Patented July 11, 111922.
1921. Serial No. 481,082.
' not be obtained from a viscous melt containing Ca (PO SiO and C. If it isdesired to practically expel P,O from a' molten bath a quite fluid melt must be obtained.
We have discovered however, that, contrary to the current belief, phosphorus may be practically completely expelled froman intimate mixture in proper proportions of phosphate rock,- sand and carbon at temperatures considerably below those which have heretofore been employed, provided the temperature is maintained just under the point of fusion of the charge. This temperature depends on the exact composition of the charge but is in the neighborhood of 1300" C., a temperature which can be attained in relatively inexpensive and simply and cheaply operated fuel fired furnaces.
Our invention may be carried out in any apparatus in which solidmaterial may be convenientl handled and efliciently heated to l300 under conditions sufiiciently non-oxidizing to prevent the burning of the carbon in the charge before it can perform its function of reducing calcium phosphate. An internally fired rotary kiln heated with a non-oxidizing flame meets these require- We do not, however, wish to be limited to the employment of a rotary kiln in carrying out our processes. When we use an internally fired rotary kiln, we prefer tobriquette the charge in order to prevent the dusting of the powder charge and in order to furnish an additional safeguard arately and are then intimately mixed in such proportions that combined CaO, and
silica, SiO are-in the molecular ratio of- 1:1 and carbon is present in at least 50% excess-of that required by the equation The actual proportions of phosphate rock, sand and coal will vary according to the composition of these materials as will be understood by thoseskilled in the art. This claim and desire to secure by mixed charge is preferably formed into briquettes according to known methods, and is then fed into an internally fired kiln in which the fuel and air are so proportioned that a reducing or at least not-strongly oxidizing atmosphere is maintained. The heat is so regulated that the charge is brought only to incipient clinkering orslightly under. Under these conditions practically all of the phosphorus is evolved 111 the elementary state. The duration of the heating necessary to secure complete expulsion of the P 0 depends on the fineness and intimacy of mixing of the materials on the physical structure of the phosphate rock, on the exact composition of the charge, etc. For an ordinary Florida or Tennessee phosphate rock the time of heating need not exceed one hour at the most if the materials are ground to a fineness under 100 mesh. The ases from the kiln, containing the expelle phosphorus may be burned under boilers or other heat conserving devices.
The oxides of phosphorus contained in the gases from the burners may be collected in any suitable manner as for instance by a Cottrell precipitator or they may be absorbed in any well known and usual manner.
It is obvious that those skilled in the art may vary the details without departing from the spirit of the invention and therefore, we do not wish .to be limited by the above disclosure except as required by the claims. 4
Having described our invention what we Letters Patent, is:
1. The process of making phosphoric acid, comprising forming an intimate mixture of phosphate rock,- siliceous material and carbonaceous material in such proportions that --the molecular ratio of combined CaO to silica will be 1:1 heating the mixture at a,
temperature notto exceed incipient clinkering until practically all the phosphorus has been expelled forming oxides of the expelled phosphorus and recovering such oxides.
2. The process of making phosphoric .acid,
comprising forming an intimate mixture of phosphate rock, siliceousmaterial and carbonaceous material insuch proportions that the molecular ratio of combined CaO to silica will be '1:1 and the carbon present will be at least in excess of that required by the equation I heating the mixtureat a temperature not to exceed that of incipient clinkering until practically all the phosphorus has been expelled, forming oxides of the expelled phosphorus and recovering such oxides.
3. The process of making phosphoric acid, comprising forming an intimate mixture of phosphate rock, silicious material and carbonaceous material in such proportions that the carbon present will be at least 50% in excess of that required by the equation heating the mixture at a temperature not to exceed that of incipient clinkering until practically all the phosphorus has been expelled, forming oxides of the expelled phosphorus and recovering such oxides.
4. The process of making phosphoric acid, comprising forming an intimate mixture of phosphaterock, silicious material and carbonaceous material in such proportions that the molecular ratio of the combined CaO to the silica will be 1 :1, forming the material so mixed into briquettes, heating the briquettes at a temperature not to exceed incipient clinkering until all the phosphorus has been expelled, forming oxides of the expelled phosphorus and recovering such oxides.
5. The process of making phosphoric acid, comprising forming an intimate mixture of phosphate rock, silicious material and carbonaceous material in such proportions that ,the molecular ratio of silica to combined to exceed that of incipient clinkering until practically all the phosphorus has beenexpelled, forming oxides of the expelled phosphorus and recovering suchoxides.
6. The process of-making phosphoric acid,
.comprising forming an intimate mixture of phosphate rock, silicious material and carbonaceous material in such proportions that the carbon present will be at least 50% in excess of that required by the equation Ga (P0 -|-3SiO',,|-5C'= 3CaSiO +2P+5CO, forming the materials so mixed into briquettes, heating the briquettes at a temperature not to exceed that of incipient clinkering until practically all the phosphorus has been expelled, forming oxides of the expelled phosphorus and recovering such oxides. 1
I ERNEST w. GUERNSEY.
JEW YAM YEE.
US481082A 1921-06-28 1921-06-28 Process of producing phosphoric acid Expired - Lifetime US1422699A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3052523A (en) * 1960-02-01 1962-09-04 Kellogg M W Co Phosphorus production
US3056659A (en) * 1960-02-26 1962-10-02 Kellogg M W Co Phosphorus production
DE1150958B (en) * 1961-02-11 1963-07-04 Giulini Ges Mit Beschraenkter Process for the production of gases containing phosphorus pentoxide
US3923961A (en) * 1970-10-05 1975-12-02 Int Minerals & Chem Corp Production of phosphorus

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3052523A (en) * 1960-02-01 1962-09-04 Kellogg M W Co Phosphorus production
US3056659A (en) * 1960-02-26 1962-10-02 Kellogg M W Co Phosphorus production
DE1150958B (en) * 1961-02-11 1963-07-04 Giulini Ges Mit Beschraenkter Process for the production of gases containing phosphorus pentoxide
US3923961A (en) * 1970-10-05 1975-12-02 Int Minerals & Chem Corp Production of phosphorus

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