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4,402,919 Process for the regeneration of mineral acids used to solubilize phosphate ores

18 Claims, No Drawings

Primary Examiner-O. R. Vertiz

Assistant Examiner-Gregory A. Heller

Attorney. Agent, or Firm-William G. Addison

A process for solubilizing uranium and other values in

an ore containing the same together with aluminum and

phosphorus and effecting regeneration of a mineral acid

employed to solubilize the ore. The regeneration is

effected by heating the spent acid solution resulting

from solubilization of the ore in a reaction zone to a

temperature above 100° C. while maintaining at least

the autogenic pressure of the heated solution within the

reaction zone. The treatment causes aluminum phosphate

to precipitate from the solution while simultaneously

causing regeneration of at least a portion of the

mineral acid in the solution that was consumed to originally

solubilize the ore. The dissolved uranium and

other elements of value can be recovered from the solution,

either before or after acid regeneration, by any

known technique. The regenerated mineral acid then

can be used to solubilize fresh ore.

United States Patent [19]

Denham et ale

[54] PROCESS FOR THE REGENERATION OF

MINERAL ACIDS USED TO SOLUBILIZE

PHOSPHATE ORES

[75] Inventors: Dale Denham, Boulder; Roland

Schmidt, Wheat Ridge, both of Colo.

[73] Assignee: Kerr-McGee Corporation, Oklahoma

City, Okla.

[21] Appl. No.: 245,386

[22] Filed: Mar. 19, 1981

[51] Int. el.3 •••••••••••••••••••••• C01G 43/00; COIB 25/16;

COlE 17/72; BOlD 11/00

[52] U.S. Cl 423/8; 423/10;

423/18; 423/319; 423/320; 423/522; 423/132

[58] Field of Search 423/6, 8, 9, 10, 321 R,

423/320, 132,522,319, 18

[56] References Cited

U.S. PATENT DOCUMENTS

2,905,526 9/1959 McCullough 423/10

FOREIGN PATENT DOCUMENTS

10267 of 1884 United Kingdom 423/132

[57]

[11]

[45]

ABSTRACT

4,402,919

Sep. 6, 1983

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4,402,919

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SUMMARY OF THE INVENTION

DESCRIPTION OF THE PREFERRED

EMBODIMENT

A feed material comprising an ore containing aluminum,

phosphorus and other values including uranium is

treated to obtain a select fraction having a particle size

less than about 150 U.S. Standard mesh and preferably

less than 200 U.S. Standard mesh to provide a concentrate

fraction. The concentrate fraction contains valuable

quantities of uranium and other elements such as

aluminum and phosphorus. The remainder of the feed

material predominately comprises quartz and is discarded.

The treatment by which the concentrate fraction

is obtained can include crushing, scrubbing, grinding

or milling of the ore to provide a particulate capable

of being sized. The particulate is sized by screening or

any other suitable means. The particular apparatus employed

can comprise any commercially available equipment

capable of producing the concentrate fraction.

fraction of large particles size quartz sand and upgrades

the unlnium, aluminum and phosphorus content of the

remainder. Acid consumption still is substantially

higher than desirable. For example, 1600 to 2000

5 pounds of 93 to 98 percent sulfuric acid are required to

dissolve 2000 pounds of concentrate. It is known that

calcining the concentrate before dissolution will reduce

acid consumption. However, acid consumption remains

at about 600 pounds of93 to 98 percent sulfuric acid per

2000 pounds of original concentrate.

It is desirable to provide a process that will permit

regeneration of a portion of the acid that is consumed to

solubilize the ore in which the uranium is present.

The surprising discovery now has been made that

uranium can be dissolved from an ore comprising aluminum,

phosphorus, uranium and other values by a procedure

which reduces the quantity of acid consumed to

effect the dissolution by over one half the quantity presently

consumed in the best prior art process. The reduction

in acid consumption is effected by regeneration of

a substantial portion of the acid consumed to solubilize

the ore.

In practice, the ore is contacted with a mineral acid to

solubilize at least a portion of the acid soluble constituents

including any uranium contained in the ore. The

ore can be physically concentrated or otherwise treated

30 such as by calcination prior to contacting the mineral

acid. The solubilization results in the formation ofa

spent acid solution containing dissolved uranium, aluminum,

phosphorus and other values together with any

undissolved solids. The spent acid solution then is

heated to a predetermined elevated temperature while

maintaining at least the autogenic pressure of the solution

to effect a precipitation of aluminum phosphate

from the solution. The precipitation results in the regeneration

of a substantial portion of the mineral acid consumed

to solubilize the ore. The uranium values then

can be recovered from the remaining solution by any

known techniques. The uranium depleted solution comprising

regenerated acid then is recycled to contact

fresh ore to solubilize additional uranium values.

Alternatively, the uranium can be recovered from the

spent acid solution prior to acid regeneration.

An additional benefit of the process is the production

of a high quality aluminum phosphate by-product.

BACKGROUND OF THE INVENTION

PROCESS FOR THE REGENERATION OF

MINERAL ACIDS USED TO SOLUBILIZE

PHOSPHATE ORES

1. Field of the Invention

This invention relates to a process for the regeneration

of mineral acids used to solubilize phosphate ores

which thereby permits recovery of uranium and other 10

valuable minerals from the ore.

2. Description of the Prior Art

It is well known in the phospheric acid technology

that phosphate ore can be treated with a mineral acid to

convert the phosphate into a soluble form, either as 15

phosphate fertilizers, phosphoric acid or phosphoric

acid compositions which can be processed into phosphate

chemicals. The solubilization process also is

known to dissolve impurities in the ore such as uranium

and vanadium which then can be separately recovered 20

from the resultant solution. One of the largest economic

expenses of the process is the cost of the mineral acid

that is consumed during the solubilization. The quantity

of mineral acid required to effect the solubilization is

directly related to the quantity of acid soluble materials 25

present in the ore. Most of the acid soluble materials are

dissolved in the process of solubilizing the phosphate

values. No simple method is known in the prior art to

regenerate the acid used to convert the phosphates into

a soluble form.

Large phosphate ore fields are known to exist in

Florida and in other areas of the United States. For

economic reasons, only the phosphate ores containing a

high ratio of phosphate to other acid soluble materials

are considered commercially recoverable. The high 35

quality commercially recoverable ores of the Florida

fields have been found to contain limited quantities of

uranium. The overburden on the high quality phosphate

ore comprises material referred to as "leached zone

material" which consists largely of sand containing 40

components of aluminum, phosphorus, iron and other

values together with clays. The leached zone material

has been formed by natural weathering or leaching of

the phosphate ore field. The low phosphate content of

this leached ore presently makes its utilization unattrac- 45

tive for the production of phosphates because of the

large quantity of mineral acid required to solubilize the

ore. However, this leached ore has been found to contain

uranium in concentrations significantly greater than

in the higher quality phosphate ore that is considered 50

commercially recoverable.

The major problem preventing the recovery of the

uranium in the Florida leached zone material and from

other phosphate ore fields is one of economics. A large

quantity of acid is required to effect dissolution of the 55

uranium present in these ores. The high acid requirement

is due to the fact that the aluminum, phosphorus

and other acid soluble values also must be dissolved to

solubilize the uranium. Further, no effective method of

physically concentrating the minerals to produce a sig- 60

nificantly higher quality concentrate for treatment has

been found.

Presently, the best known concentrating procedure

produces a concentrate of the uranium and other phosphate

minerals by scrubbing and sizing the raw ore to 65

obtain a select fraction which then is dissolved with a

mineral acid. This procedure rejects from about 60 to

about 75 percent of the ore, by weight, as a coarse

~ ~ • • "I _ -_ .. • ' .... •

. . . - . .' . ~ ..

4,402,919

3

The concentrate fraction then is admixed with a sufficient

quantity of a leach solution comprising a mineral

acid to effect solubilization of a substantial portion of

the concentrate fraction and at least a portion of the

uranium present in said concentrate fraction. The min- 5

eral acid can comprise, for example, sulfuric acid, phosphoric

acid and the like. In a typical reaction, alSO

mesh size fraction in aqueous slurry form, having a

solids content in the range of from about 30 percent to

about 60 percent, is reacted with the sulfuric acid at 10

temperatures in a range between about ambient temperature

to above the boiling temperature of the leach

solution and preferably from about 60° C. to about 90°

C. For temperatures above the boiling temperature of

the leach solution, the solubilization is effected under a 15

pressure at least equal to the autogenic pressure of the

heated solution.

Preferably, the solubilization is carried out for a period

of time ranging between 0.2 and about 15 hours and

more particularly, for a period of from about 30 minutes 20

to about 60 minutes, although the length of time may be

varied considerably depending upon other variables in

the reaction conditions. The interdependence of variables

makes for vast differences in the specific conditions

employed as to each variation. In general, it may 25

be stated the higher the percent acid acidulation used,

the shorter the time required. Thus, for example, if

about 70 percent acidulation is used, that is, about 106.5

pounds of 96 percent sulfuric acid per 100 pounds of

ore, only about 15 minutes is required to acomplish the 30

digestion, while at about 45 percent acidulation, about 6

hours digestion is necessary to give good recovery of

the desired constituents. Depending upon the analysis

of the particular ore processed, between about 30 percent

and 105 percent acidulation is desired. This corre- 35

sponds to the addition of between about 29 pounds and

about 150 pounds of sulfuric acid per hundred pounds of

ore processed. Preferably, about 70 percent acidulation

is used. The percent acidulation referred to in this description

is calculated on the basis of the reaction of 40

sulfuric acid with all of the aluminum, calcium and iron,

or other significant cationic constituents present in the

ore. In other words, 100 percent acidulation would be

the addition of that amount of sulfuric acid required to

completely react with these components. After the 45

solubilization, the aqueous solution of reaction products,

sometimes referred to as "spent acid solution," is

separated from the insolubles, such as quartz and clay.

The substantially solids-free aqueous solution of reaction

products is introduced into a reaction zone wherein 50

the solution is heated to a temperature above 100° C.

while maintaining the solution at a pressure level at least

equal to the autogenic pressure of the solution to effect

a precipitation of the leached phosphorus values as

crystalline aluminum phosphate. Preferably, the aque- 55

ous solution is heated to a temperature level in the range

offrom about 150° C. to about 200° C. and most preferably

a temperature in the range of from about 180° C. to

about 200° C. Temperatures above 200° C. can be employed

to effect the precipitation of the leached phos- 60

phorus values, however, the precipitation reaction is

essentially complete at about 200° C.

The present inventors have found that when the

leached phosphorus values are precipitated within the

aqueous solution, in the described manner, that a por- 65

tion of the mineral acid is regenerated. This is evidenced

by a significant drop in the pH level of the aqueous

solution of reaction products as the aluminum phos-

4

phate precipitate is formed. The aqueous slurry produced

at a result of the precipitation of the AIP04 also

contains other values, including uranium, that were

dissolved during solubilization of the ore. These additional

elements remain in the solution and generally do

not precipitate with the aluminum phosphate.

While the precise mechanism of the chemical reaction

involved in regeneration of the mineral acid presently

in unknown, the inventors presently believe that

the major portion of the aluminum and phosphorus

contained in the aqueous solution of reaction products,

resulting from solubilization of the ore, is in the form of

AIH2P04+2. It is believed that the mineral acid is regenerated

according to the following equation:

AIHZP04+Z+mineral acid

anion~AIP04ppl+ mineral acid

More particularly, when sulfuric acid is employed to

solubilize the ore, the acid is believed to be regenerated

according to the following equation:

An analysis of the precipitate employing x-ray diffraction

indicates that the precipitate comprises berlinite, an

anhydrous aluminum phosphate. Further, chemical

analysis of the precipitate indicates that it contains no

detectable quantity of uranium and no significant quantity

of any of the other solubilized mineral values present

in the aqueous solution of reaction products, the

precipitate being found to have a purity in excess of 99

percent aluminum phosphate. Thus, the process of this

invention also produces a high quality by-product that

has a significantly higher P20S content than, for example,

apatite, which is considered a high quality source of

phosphorus.

The precipitated aluminum phosphate can be separated

from the aqueous slurry of the same by filtration,

centrifugation gravity settling or the like. The particular

apparatus employed to effect the separation can

comprise any of that which commercially is available.

In one particular embodiment in which the mineral

acid comprises sulfuric acid, if an attempt is made to

precipitate the aluminum and phosphorus from the

aqueous solution of reaction products at a temperature

below about 100° C., a precipitate will form. However,

the precipitate is alunogen (Ab(S04h.18H20) and no

mineral acid is regenerated. When sulfuric acid comprises

the mineral acid, it also has been observed that

any calcium sulfate which may tend to precipitate from

the aqueous solution of reaction products after formation

of such solution should be permitted to form. The

precipitated calcium sulfate then should be separated

from the aqueous solution before introduction of the

now substantially solids-free aqueous solution into the

reaction zone to precipitate the aluminum phosphate.

Otherwise, a mixed calcium aluminum sulfate is found

to precipitate instead of aluminum phosphate and no

sulfuric acid is regenerated.

The presence of calcium in the aqueous solution

when mineral acids other than aulfuric acid are employed

to effect the solubilization of the ore has no

apparent effect upon the precipitation of the aluminum

and phosphorus values as aluminum phosphate. The

filtrate remaining after separation of the aluminum

phosphate, which contains dissolved uranium and other

4,402,919

EXAMPLE II

5

elements, can be treated by any known method to recover

the uranium and any other desired elements.

The uranium can be separated from the filtrate by, for

example, solvent extraction techniques whereby the

uranium values are transferred from the aqueous filtrate 5

to an organic solvent extractant. The extracted uranium

then is separated from the organic solvent by, for example,

contact with an alkaline stripping agent. Various

processes for solvent extraction of tranium and other

values from aqueous acidic solutions are disclosed in, 10

for example, U.S. Pat. Nos. 3,700,415, 3,711,591 and

3,836,476, the disclosures of which are incorporated

herein by reference. It is to be understood that the

method for separating the uranium or any other values

from the aqueous solution is not to be limited to solvent 15

extraction processes but that any method known by

individuals skilled in the art may be employed.

The practice of the process of the present invention

results in the regeneration of over 50 percent of the acid

employed to solubilize the ore. Often, the present pro- 20

cess effects regeneration of over two thirds of the mineral

acid originally employed to solubilize the ore. Such

regeneration capability permits applicants to recover

uranium present in low phosphate content ores in an

economical manner while also providing a high purity 25

by-product of aluminum phosphate which can be used

as a feed stock for production of aluminum and phosphorus

chemicals.

To further illustrate the process of the present invention,

and not by way of limitation, the following exam- 30

pIes are provided.

EXAMPLE I

A representative sample of an aqueous solution of

reaction products resulting from sulfuric acid leaching 35

of a minus 150 mesh fraction of Florida leached zone

material is introduced into a reaction zone comprising a

Parr autoclave having an acid resistant liner. The solution

is formed by contacting 1600 lbs. of 96 percent

H2S04 with one ton of uncalcined leached zone mate- 40

rial. The aqueous solution is analyzed and is found to

contain 55.3 gil Ah03, 30 gil P20S, 0.11 gil U30g and

have a pH of about 0.5. The aqueous solution is heated

in the reaction zone to a temperature of about 200· C.

while maintaining the autogenic pressure of the aqueous 45

solution. The solution· is maintained at the elevated

temperature for about 5 minutes to effect precipitation

of crystalline aluminum phosphate in the solution to

form a slurry. The slurry is withdrawn from the reaction

zone and filtered to separate the precipitate from 50

the aqueous solution. The precipitate is assayed and is

found to comprise in excess of 99 percent aluminum

phosphate and less than 0.001 percent U30g. The pH

level of the filtrate is measured and is found to be about

0.2. The filtrate is analyzed and is found to contain 23 55

gil Ah03 and 3.7 gil P20S.

The formation of the aluminum phosphate precipitate

is found to regenerate an amount of mineral acid equivalent

to in excess of 800 lbs. of 96 percent sulfuric acid

per ton of original leached zone material. This repre- 60

sents in excess of about 50 percent of the acid necessary

to solubilize a similar quantity of the leached zone material.

65

A representative sample of an aqueous solution of

reaction products resulting from sulfuric acid leaching

of a minus 150 mesh fraction of calcined leached zone

6

material is introduced into a reaction zone comprising a

modified Parr autoclave. The solution is formed by

contacting 600 lbs. of 96 percent H2S04 with one ton of

leached zone material that is calcined prior to contact

with the acid. The aqueous solution is analyzed and is

found to contain 100 gil Ah03, 120 gil P20S, 0.3 gil

U30g and have a pH of about 1.3. The aqueous solution

is heated in tlIe reaction zone to a temperature of about

200· C. while maintaining the autogenic pressure of the

aqueous solution. The solution is maintained at the elevated

temperature for about 5 minutes to effect precipitation

of crystalline aluminum phosphate in the solution

to form a slurry. The slurry is withdrawn from the

reaction zone and filtered to separate the precipitate

from the aqueous solution. The precipitate is assayed

and is found to comprise in excess of 99 percent aluminum

phosphate and less than 0.001 percent U30g. The

pH level of the filtrate is measured and is found to be

about 0.5. The filtrate is analyzed and is found to contain

39.5 gil Ah03 and 36.4 gil P20S.

The formation ofthe aluminum phosphate precipitate

is found to regenerate an amount of mineral acid equivalent

to in excess of 420 lbs. of 96 percent sulfuric acid

per ton of original leached zone material. This represents

in excess of about 70 percent of the acid necessary

to solubilize a similar quantity of the leached zone material.

While the present invention has been described with

respect to what at present are the preferred embodiments

thereof, it will be understood, of course, that

certain changes, substitutions, modifications and the like

can be made therein without departing from its true

scope as defined in the appended claims.

What is claimed is:

1. A process for the regeneration of mineral acid used

to solubilize phosphate ore comprising:

contacting an ore comprising aluminum, phosphorus

and other values including uranium with a leach

solution comprising a mineral acid selected from

the group consisting of phosphoric acid and sulfuric

acid to solubilize at least a portion thereof and

form a solution of spent mineral acid and solubilized

values in association with any non-solubilized

values, said solubilized values including aluminum,

phosphorus and uranium;

introducing said solution of spent mineral acid and

solubilized values into a reaction zone; and

heating said solution to said reaction zone to a temperature

in excess of 100· C. while maintaining the

pressure level at least equal to the autogenic pressure

of said solution to cause a substantially uranium-

free precipitate of crystalline aluminum phosphate

to form and to regenerate at least a portion of

said spent mineral acid to form regenerated leach

solution containing solubilized uranium values.

2. The process of claim 1 defined further to include

the steps of:

contacting said regenerated leach solution with an

organic extractant to extract at least a portion of

any solubilized uranium values present therein; and

recovering said extracted uranium values from said

organic extractant.

3. The process of claim 1 defined further to include

the steps of:

contacting said solution of spent mineral acid and

solubilized values, prior to heating said solution,

with an organic extractant it} I'lxtract at least l\

4,402,919

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9. The process of claim 8 wherein the temperature to

which the solution is heated in the reaction zone is in the

range of from about 150° C. to about 200° C.

10. The process of claim 8 wherein the temperature to

which the solution is heated in the reaction zone is in the

range of from about 180° C. to about 200° C.

11. The process of claim 8 wherein at least 50 percent

of the mineral acid employed to solubilize the ore is

regenerated.

12. The process of claim 8 wherein at least 70 percent

of the mineral acid employed to solubilize the ore is

regenerated.

13. The process of claim 8 defined further to include

the steps of:

contacting said aqueous solution of reaction products,

prior to heating in said reaction zone, with an organic

extractant to extract at least a portion of any

solubilized uranium values present in said aqueous

solution; and

recovering said uranium values from said organic

extractant.

14. The process of claim 8 defined further to include

the steps of:

contacting said regenerated aqueous leach solution

with an organic extractant to extract at least a

portion of any solubilized uranium values present

therein; and

recovering said extracted uranium values from said

organic extractant.

15. The process of claim 2 defined further to include

the step of:

contacting fresh ore with the uranium-depleted regenerated

leach solution to solubilize at least a

portion of said fresh ore.

16. The process of claim 3 defined further to include

the step of:

contacting fresh ore with the regenerated leach solution

to solubilize at least a portion ofSaid fresh ore.

17. The process of claim 13 defined further to include

the step of:

contacting fresh ore with the regenerated leach solution

to solubilize at least a portion of said fresh ore.

18. The process of claim 14 defined further to include

the step of:

contacting fresh ore with the uranium-depleted regenerated

leach solution to solubilize at least a

portion of said fresh ore.

* * :(I: * *

10

7

portion of any solubilized uranium values present

in said solution; and

recovering said uranium values from said organic

extractant.

4. The process of claim 1 wherein the ore comprises 5

leached zone material.

5. The process of claim 1 wherein the temperature to

which the solution is heated in the reaction zone is in the

range of from about 100° C. to about 200° C.

6. The process of claim 1 wherein the temperature to

which the solution is heated in the reaction zone is in the

range of from about 150° C. to about 200° C.

7. The process of claim 1 wherein the temperature to

which the solution is heated in the reaction zone is in the 15

range of from about 180° C. to about 200° C.

8. A process for the regeneration of mineral acid used

to solubilize phosphate ore comprising: .

separating an ore comprising aluminum, phosphorus,

uranium and other elements into at least two frac- 20

tions, at least one of said fractions having an average

ore particle of a size capable of passing through

a U.S. Standard 150 mesh screen;

contacting said fraction capable of passage through a 25

U.S. Standard 150 mesh screen with an aqueous

leach solution comprising a mineral acid selected

from the group consisting of phosphoric acid and

sulfuric acid to solubilize at least a portion thereof

and form an aqueous solution of reaction products 30

comprising spent mineral acid and solubilized values,

said solubilized values including aluminum,

phosphorus and uranium;

separating said aqueous solution of reaction products

from any unsolubilized ore to provide a substan- 35

tially solids-free solution of reaction products;

introducing said substantially solids-free solution of

reaction products into a reaction zone; and

heating said solution in said reaction zone to a tem- 40

perature in the range of from about 100° C. to

about200° C. while maintaining the pressure level

at least equal to the autogenic pressure of said solution

to cause a precipitate of substantially uraniumfree

crystalline aluminum phosphate to fonn and to 45

cause at least a portion of said spent mineral acid to

.regenerate and fonn regenerated aqueous leach

solution containing solubilized uranium values.

50

55

60

65

denHor��i't� x8o further heat the water vapor and to

 

further heat the recycle gas; and

(f) introducing the water vapor and the reformed

recycle gas into the reactor.

* * * * *

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45

50

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60

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