Wet granulation method for generating granules

Information

  • Patent Grant
  • 6454979
  • Patent Number
    6,454,979
  • Date Filed
    Friday, April 17, 1998
    26 years ago
  • Date Issued
    Tuesday, September 24, 2002
    22 years ago
Abstract
A method of wet granulation of fertilizer and other materials into granules. The method involves formation of the granule directly on the pan from the feedstock without intermediate steps or the use of seed materials. The result is a product having a completely uniform cross section. The feedstock is initially in the size distribution of −150 mesh with 90% or greater in the size range of 200 mesh. Moisture is maintained to facilitate a steady process without cycling.
Description




FIELD OF THE INVENTION




The present invention relates to a pan granulation method for pan granulating pellets or granules and more particularly, the present invention relates to a wet granulation method for granulating fertilizer and other materials into industrially useful pellets or granules.




BACKGROUND OF THE INVENTION




One of the greatest limitations existing in the granulation art is centered on the fact that known processes require a seeding agent in order to achieve the proper conditions for material accretion to result in a pellet or granule. By making use of a seed, the resulting granule is adversely affected in two key properties; roundness and cross sectional uniformity. Typically, seeding material is not round and as the precursor particle, the result is irregular initial feedstock accretion which, in turn, forms an out-of-round particle upon which further material accretes. A further detriment from this results in terms of nonuniform particle density.




Methodology is required for synthesizing a granule in the absence of seed material and which is round, tightly packed with a uniform homogeneous cross section and capable of eliminating hazards associated with fertilizer granule production.




One of the latest issued patents in the art to which the present invention relates is U.S. Pat. No. 5,460,765, issued to Derdall et al., Oct. 24, 1995. The reference teaches a process for pan granulating a particulate material. Based on the teachings of the Derdall et al. reference, a final particle size distribution that is achievable by practicing the invention is between about −5 mesh to about +10 mesh. In order to initiate the process, the Derdall et al. process is limited to the introduction of a seeding material typically between about −14 mesh and +28 mesh. This is required in order to control the granule growth and as indicated in the Derdall et al. disclosure, seed minimizes mutual agglomeration and results in high yields being obtained. The Derdall et al. reference further indicates that the proper sizing of the seed is fundamental to the operation of the process for granulation in order to have product yields exceed 90%. Reference is made in the disclosure that a seed core in the range of −14 mesh to +35 mesh is required in order to achieve a steady state and maintain uniform size distribution of between −8 mesh to +6 mesh.




The Derdall et al. process, although a meritorious procedure, did not recognize the limitations of employing a seeding agent or the need for controlling the dust generated during granulation which not only creates an unhealthy environment for workers, but more seriously, results in a potentially explosive environment. This is evident from the teachings of Derdall et al., particularly at column 3, beginning at line 24, wherein it is stated:




“It may be more difficult to keep the granulation steady or stable with fine seed, such as −35 mesh.”




The difficulty to which the Derdall et al. disclosure alludes is directed to cycling which is an inherent problem with pan granulation processes. If the size distribution of the seeding agent is not constant, then the process will not stabilize and effectively “cycles” as is known to those skilled in this art. The result of this is that larger formed granules on the pan effectively destroy the smaller particles. This, of course, defeats the purpose of the pan granulation to generate particles.




Furthermore, at line 36 in column 3, the disclosure indicates that:




“Fine seed sizes can be used, such as +35 mesh, but a point is reached where over-seeding or nucleation occurs easily and causes the final product yield to drop down.”




It is also indicated at column 3, beginning at line 45 that:




“Seed material in the range of 20 mesh is the best single point for each of control and uniformity of product size distribution . . . ”.




As is known, the larger the mesh numerical value the smaller the micron size of the particle. The following mesh sizes correspond to the stated micron sizes:




















Approximate







Mesh Size




Micron Size



























12




1680







16




1190







20




840







30




590







40




420







100




149







200




74















Based on the teachings of the Derdall et al. disclosure, mesh sizes greater than +35 caused potential nucleation problems and result in a final product yield to decrease. With the technology disclosed, infra, it has been found that by using a fine powder of between −35 mesh to +150 mesh, that the superior quality product can be formed in high yield and typically in the range of a greater than 90% yield. When the above passage regarding Derdall et al. is considered, it is clear that Derdall et al. effectively contradict what the technology set forth herein has found to be particularly successful.




In the present application the size distribution of the nucleating material is between −35 mesh and +150 mesh which corresponds to micron size less than 590 μm and 105 μm, respectively. Nowhere in the prior apart is a powdered nucleating agent in this size distribution disclosed for the purpose of forming a uniform granule in the size distribution of −8 mesh to +4 mesh. Advantages have been ascribed to this process and one of the most attractive advantages is that the granule or pellet has an enormous break strength and a uniform cross section. It has been found by practicing the present invention, that break strengths in the range of 1 to 4 kgs or greater have been achieved.




In the Derdall et al. disclosure, at column 3, beginning at line 33 it is stated:




“Seed of large size forms granules of very poor strength.”




If one considers these teachings in light of the size of the nucleating agent provided herein, the admissions made in the Derdall et al. disclosure would clearly go against the appeal of using a seeding agent in the size range as clearly taught by Derdall et al. The; instruction in Derdall et al. indicates an ideal seeding agent size is 20 mesh (supra); the instant application uses a powder having a particle size between 75-750% smaller than Derdall et al. and yet achieve very desirable results.




In Statutory Invention Registration H1070, authored by Harrison et al., Jul. 7, 1992, a method for granulating potash materials is disclosed. The process involves the conversion of particulate potassium sulfate or potassium chloride by agglomeration using a conventional rotary drum granulator, pan granulator or other conventional granulating device.




In the disclosure of this document, there are no specific teachings regarding the elimination of a seeding agent, feedstock size or other important factors related to process control in order to generate superior quality granules having commercial viability. Further, the process clearly is an agglomeration process. It is known that agglomeration typically involves the aggregation of colloidal particles suspended in a liquid into clusters or flocs. These clusters or flocs have varying degrees of interstices and are loosely bound (


Hawley's Condensed Chemical Dictionary,


eleventh edition, 1987).




As a particularly advantageous feature of the present invention, the methodology herein facilitates sulfur granulation. With the effectiveness of air pollution regulations, it has now become necessary to augment the soil with sulfur due to deficiencies. As is generally known in agricultural science, sulfur fertilization increases crop yield and quality and further has an effect on nitrogen processing by plant matter. This processing is, in turn, related to protein synthesis, nitrogen fixation, photosynthesis and disease resistance.




Currently, sulfur pelletizing or granulation processes proceed according to dry synthesis methodology. This is extremely hazardous since sulfur, particularly sulfur dust, is explosive and difficult to handle. In view of these serious limitations, the field is in need of a viable and safe granulation process. The present technology set forth herein delineates a nonhazardous method for granulating sulfur, customizing particle size as well as additive addition to produce sulfur particles capable of slow release, pesticidal, herbicidal and bactericidal activity inter alia.




Wet granulation is inherently complicated, since irregular particle crystallography is inherently difficult to control. Wet powder is not uniform and this leads to non-uniform accretion, over nucleation and eventual breakdown of the process. For these reasons among others, the art has not realized an effective and viable process for wet granulation.




Boeglin et al. in U.S. Pat. No. 3,853,490, discloses a granulation method for granulating potassium sulfate. The method involves the use of large particle starting material −6 +65 mesh (50%), −200 mesh (10% to 30%) and the remainder comprising −65 +200 mesh. In the disclosure it is stated that the granulation is carried out in conventional granulating equipment, however, there is no discussion concerning process control difficulties associated with pan granulation of the product. It is known from Derdall et al. that significant difficulties are encountered in keeping the granulation steady even with seed material in the size range of +35 mesh. The most difficult problem is controlling “cycling” where the larger particles destroy the smaller particles. The Boeglin et al. reference would therefore appear to be directed solely to a drum granulation process where the complications inherent with pan granulation are not encountered.




In U.S. Pat. No. 3,711,254, issued to McGowan et al., there is discussed a process for granulating potash. The disclosure of the document only provides a cursory teaching of granulation and includes pan and drum granulation within the same process.




Kurtz, in U.S. Pat. No. 5,322,532, discloses a sodium bicarbonate blast media. The blast media comprises an agglomeration of sodium bicarbonate and sodium sesquicarbonate. The reference does not set forth any details with respect to any other formulation process apart from agglomeration and lacks instruction regarding any other material for augmentation.




Other patent documents of only marginal relevance include the following U.S. Pat. Nos.: 4,371,481; 4,131,668; 4,264,543; 5,108,481; 3,206,508; 3,206,528; 4,344,747; and, 5,124,104,




The prior art, when taken singly or collectively, is deficient any clear teachings regarding the preparation of fertilizer, blasting, deodorizer or water softener granules having the following commercial and industrial advantages:




a) uniform cross section;




b) tightly packed feedstock;




c) absence of a seed or crystal core;




d) increased break strength relative to the prior art;




e) material homogeneity throughout the granule; and




f) greater quantity of feedstock material per granule




There has been a long felt need for granules having these desirable properties and for methodology to effect synthesis of such products; the present invention addresses these needs in an elegant and efficacious manner.




SUMMARY OF THE INVENTION




One object of the present invention is to provide an improved method for generating a variety of industrially useful particles or granules, which particles are devoid the drawbacks of the prior art techniques.




A further object of one embodiment of the present invention is to provide a wet granulation method for granulating a feedstock into granules, comprising the steps of:




providing a feedstock having about 99.9% particle size of −150 mesh of 99.9% particle size of −150 mesh about 90% comprising a particle size of −200 mesh;




providing a binder material in an amount of about 6% to about 8% by weight;




contacting the feedstock with the binder on a pan granulator under moisture conditions where the moisture content on the pan is between about 1.5% to about 11% by weight; and




forming granules on the pan directly from the feedstock in the absence of seed or nucleating material.




In the present invention, the maintenance of moisture on the pan and in the product substantially prevents dust formation during product synthesis. This is augmented by the addition of oil e.g. mineral, vegetable, seed, synthetic, etc. to the final product. As a further feature, plant nutrients, growth regulators, minerals, time release compositions and suitable bacteria may be included in the granules. In terms of the nutrients, suitable examples include nitrogen, phosphorous and potassium; the growth regulators may be herbicides, pesticides, hormones; the minerals will vary depending on soil and environment conditions, but may include copper, boron and other metals; the time release materials may be selected to release the sulfur only at specific times during the growth cycle of the plant, crop, etc.; bacteria may be selected from a diverse variety depending on the specific requirements of the user. To this end, sulfur oxidizing bacteria may be selected, disease combating bacteria to reduce the vulnerability of the crop etc.




As another feature of the present invention,, the technology can be easily employed in the granulation of pellets/granules used in other fields outside of the agricultural sciences. One such field is the blasting art. In this field, it is well known that sodium bicarbonate is a useful blasting medium in view of the copious benefits associated therewith. The bicarbonate is useful, but the crystals are such that high efficiency in coating removal from a substrate is not entirely practical. The present technology facilitates granulation of the bicarbonate with further crystalline materials to augment the abrasiveness of the granule.




The important inventive concept of the present invention is the ability to generate particles/granules in the absence of a seeding agent. In this manner, the process can be loosely referred to as a pan nucleation process; the process proceeds generally as crystallization, i.e., a nucleation site accretes the surrounding material. With the present technology, the pan rotation and binder assist in the material accretion around the nucleation site to produce a tightly packed granule with high feedstock content.




Having thus described the invention, reference will now be made to the accompanying drawing illustrating preferred embodiments.











BRIEF DESCRIPTION OF THE DRAWINGS





FIG. 1

illustrates a schematic representation of the method according to one embodiment of the present invention;





FIG. 2

is a photograph of a sulfur granule in cross section formulated by practicing the prior art methodology;





FIG. 3

is a photograph of the sulfur granule of

FIG. 2

;





FIG. 4

is a photograph of sulfur granules in cross section formulated by practicing the methodology of one embodiment the present invention;





FIG. 5

is a photograph of the sulfur granules of

FIG. 4

;





FIG. 6

is a photograph of a potassium chloride granules formulated by practicing the methodology of the prior art;





FIG. 7

is a photograph of red potassium chloride granules in cross section formulated by practicing the prior art methodology;





FIG. 8

is a photograph of potassium chloride granules in cross section formulated by practicing the methodology of one embodiment of the present invention;





FIG. 9

is a photograph of a potassium chloride granule illustrated in

FIG. 8

; and





FIG. 10

is a photograph of potassium chloride granules containing sulfur and formulated by practicing the methodology of one embodiment of the present invention;




Similar numerals employed in the text denote similar elements.











DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS




Prior to the explanation of the method, the following table sets forth some general properties of the compounds and materials that may be granulated.












TABLE 1











GENERAL PROPERTIES



















MELTING




BOILING







COMPOUND




CRYSTALS




SOLUBILITY




POINT (C.)




POINT (C.)




HAZARDS



















Ammonium




colorless




soluble in water,




169.6




Decomposes




may






Nitrate-





alcohol and





at 210




explode if






NH4NO3





alkalies






confined











and











exposed to











high











temperature






Ammonium




brownish white




soluble in water




513





none






Sulfate-




to gray






(NH4)2SO4






Potassium




colorless or




soluble in water;




772




sublimes at




none






Chloride-KCl




white




slightly in





1500








alcohol






Potassium




transparent,




soluble in water




337




decomposes




fire/






Nitrate KNO3




colorless or




or glycerol;





at 400




explosion







white; powder




slightly soluble






risk upon







or crystalline




in alcohol






shock or











heating or











when in











contact with











organic











materials






Potassium




colorless or




soluble in water




1072





none






Sulfate K2SO4




white hard







crystals or







powder






Sulfur-S




alpha form




slightly soluble




alpha





combustible







rhombic,




in alcohol and




approx





in finely







octahedral




ether, soluble in




94.5





divided form







yellow crystals;




carbon disulfide;




Beta





a fire and







beta form




carbon




approx





explosion







monoclinic,




tetrachloride and




119





risk exists







prismatic pale




benzene







yellow crystals






Urea




white crystals




soluble in water




132.7




Decomposes




none






CO(NH2)2




or powder




alcohol and








benzene






Sodium




white powder




soluble in water




loses





none






Bicarbonate




or crystalline





carbon






NaHCO3




lumps





dioxide at









270














Referring now to

FIG. 1

, shown is an overall schematic representation of the process according to one embodiment.




In the embodiment shown, the circuit is representative of a ten ton per hour circuit. Reference numeral


10


denotes the introduction of feedstock which may be any suitable material, numerous examples of which have been indicated supra. The technology set forth herein permits the formation of most any granulated product including various sulfates, soda ash, sulfur, potash, kaolin, magnesia, potassium sodium and ammonium chloride inter alia.




The feed may be introduced at 9.8 tons per hour (9.8 thr−1) along with suitable binder material as set forth herein previously. The feedstock and binder maybe then introduced into a pulverizer


12


to pulverize the feedstock such that a product is produced having 99.9% −150 mesh and at least 90% −200 mesh. The pulverizer


12


may be a classifying pulverizer or air sweep pulverizer or any other suitable pulverizer known by those skilled in the art. Once pulverized, the stream, generally represented by numeral


14


, is introduced into a sealed collection hopper, globally denoted by numeral


16


, which includes a bag house


18


to collect dust. Collection hopper


16


includes suitable valve


20


for metering dust into a collection bin


22


. The bin


22


is mounted over two feeders


24


and


26


which divide the material being received from bin


22


into two streams, the first stream being fed by feeder


26


to a wet mixer (not shown) and then to a first large pan granulator


28


at a rate of 7.6 tons per hour (7.6 thr


−1


), as an example, while feeder


24


feeds a second stream into a paddle or pin mixer (not shown) and then to a second pan granulator


30


, being smaller than granulator


28


. The feed rate to the small pan may be 2.8 tons per hour (2.8 thr


−1


), as an example, to, be consistent with a ten ton per hour circuit. The mixers each contain a mixture of binder and feedstock with a moisture content in the range of 4% to about 8% by weight. The material fed from the mixers to the pans is thus wet and this avoids dust formation during processing. The amount of moisture in the binder is a variable factor and is dependent upon the nature of the binder (solid/moisture content). Clearly, high moisture content binders will not require as great an addition (on a percentage by weight basis) to the mixers as the lower moisture content binders.




Pan


30


is equipped with a small receptacle


32


for retaining −35 mesh dry raw feedstock (not shown). The receptacle


32


is equipped with a variable rate metering apparatus (not shown). The feeder removes the material form the receptacle


32


and introduces the dry raw feedstock into pan


30


. As is known in the art, the pan granulators


28


and


30


include upper and lower scrapers


34


,


36


and


38


,


40


, respectively. Regarding the feedstock from receptacle


32


, the same is introduced to the pan


30


behind top scraper


38


. In this example, the production rate for the pan


30


would be set for 3 tons per hour (3 thr


−1


) with a size distribution of approximately 80% product between −8 mesh to +20 mesh. It has been found that this is achievable by combining the raw feedstock to the dust at a ratio of 1:20 to 1:100 parts. The use of an atomizing hot binder solution at any position from the 12 o'clock through to the 5 o'clock position has been found to be particularly useful. When the correct free moisture is attained, generally between 1.5% to about 11%, the first pan stabilizes at a steady state condition. In this manner, granules are formed directly on pan


30


in the absence of a seeding agent.




As indicated above, the product formed from pan


30


is typically between 50 to 80% −8 mesh. The product is discharged and dried with dryer


39


. Dryer


39


be selected from, for example, Carrier dryers, tray dryers or roto louver type dryers. The product being formed in large pan


28


is additionally transported to dryer


39


via a suitable conveyer, globally denoted by numeral


41


.




Product exiting dryer


38


via stream


42


is then screened by a suitable screening arrangement


44


at 4 mesh, 8 mesh and 20 mesh. The +4 and −20 mesh portions are sent to pulverizer


12


for recycling into the system, the recycling stream being indicated by numeral


46


. The −4 to +8 mesh portion is the final product and leaves screen


44


, as indicated by numeral


48


, as a final finished product. The −8 to +20 mesh portion is sent via stream


50


to a hopper equipped with a weigh belt feeder, broadly denoted by numeral


52


. The material is advanced from the weigh belt feeder


52


into pan


28


whereupon the product is further processed by the introduction of binder and additional dust to produce a desired granule product. This is an optional step dependent upon whether further feedstock accretion is desired.




Any residual dust which may be present in dryer


39


may be passed via line


54


for exiting dryer


39


to hopper


56


and the collected material in hopper


56


either passed onto the bag house


18


via line


58


or passed into the feedstock via line


60


. The fines or dust entering bag house


18


may additionally be passed off onto ancillary operations, for example, wet scrubbing, as broadly denoted by numeral


60


in FIG.


1


. Other examples will be readily apparent to those skilled in the art.




The ratio of −8 to +20 mesh product needed to run pan


28


at a steady state has been found to be, for the system described herein, between 1:10 to 2:5, an optimum of 1:5. Pan


28


stabilizes quickly and produces yields of greater than 95% on +8 to −4 mesh. The process yield from the overall circuit as set forth herein exceeds 90%. As discussed briefly herein previously, 10% of the weight, which is in the −20 and +4 mesh size distribution, as well as dryer dusts, can be recycled to enhance the efficiency and productivity of the method to produce maximum yields at very low cost.




With further reference to the pans


28


and


30


, as is known, the pans may be adjusted for angle and rotational speed such that the +8 to −4 mesh granules are only produced. In addition, it has been found advantageous to not only change the horizontal disposition of the pans, but also to laterally tilt the pans to enhance the efficiency of the granulating process. The specific angle of tilt and horizontal angle will be dependent upon the rotational speed and the size of the granule desired to be produced. As a variation, the tilt and/or angular velocity of the pan(s) may be adjusted to produce granules in the size distribution of −10 mesh to about 100 mesh.




It will be appreciated that the method for operation as discussed can be a single operation or may be incorporated into a unit operation within a series of other operations. This will depend upon the specific needs of the user.




It will also be readily appreciated that any number of pans can be incorporated into the system to progressively grow or accrete a granule. To this end, the process is interruptible and therefore can be custom designed to produce granules having a variety of layers of material to produce a host of valuable granules. It will be clear to those skilled in the art that the process is effective for producing a number of different forms of fertilizer and has particular utility with respect to the formation of high grade fertilizer for use on golf courses, time release formulae etc.




In terms of the binder, suitable examples include lignosol, sugars, saturated salts and proteins, water, calcium sulfate, sodium sulfate, potassium chloride, dry gluttens, wheat grains, barley grains, rice grains and calcium phosphate among others. The choice of the binder will depend on the desired characteristics of the granule and accordingly, the aforementioned examples are only exemplary. In the instance where the material to be granulated is dangerous or has the characteristic of having explosive dust, the binder composition may comprise a high moisture content, generally 30% to 60% moisture or greater with the balance comprising solids. It is also contemplated that mixtures of binder material may be employed.




With respect to the feedstock and binder, where the binder contains a higher moisture content, the use of an atomizer for dispensing moisture on to pans


28


and/or


30


may not be necessary. In a further variation, binder and feedstock material may be added to the pan(s) simultaneously. These process variations will be dependent upon the nature of the material to be pelletized or granulated.




Referring now to the photographs,

FIG. 2

illustrates granulated sulfur pellets with an ammonium sulfate core created by the prior art technique as taught by Derdall et al. The pellets clearly include a sizeable core occupying a large amount of the volume of the particle. It is also evident that the cross section of the particles is nonuniform and in some cases hollow in localized areas. In addition, the particles are not spherical, but rather substantially aspherical. These factors all depreciate the quality and industrial value of the particles.





FIG. 3

shows whole granulated sulfur pellets synthesized in accordance with the Derdall et al. methodology. As is evident from the figure, the exterior of the granules is loose to provide a grainy surface texture. This lack of consolidation of the material results in the generation of dust which, as indicated supra, creates significant handling problems and in particular, increases the likelihood of a potential explosion.




In contrast to the above,

FIGS. 4 and 5

demonstrate the high quality particles generated by the present methodology. Of particular significance is the fact that the particles/granules are completely devoid of any core or seed, but rather are entirely uniform, continuous and solid throughout.

FIG. 5

illustrates the granules in toto. It is readily apparent that the granules have a different surface appearance than those formulated by the prior art; this is further evinced by the lack of dust or grains surrounding the particles. The particles are significantly more consolidated, harder, tightly packed and include a greater amount of feedstock (at least 95% by weight) than the prior art granules. Accordingly, the, advantages enumerated herein previously are realized.




In respect of

FIGS. 6 and 7

, shown are potassium chloride granules made by the technique set forth by Derdall et al. The Figures illustrate two different forms of the compound and confirm the presence of the seed indicated as a critical factor to the generation of the particles.




With reference to

FIGS. 8 and 10

, shown are potassium chloride particles formulated by practicing the methodology of one embodiment of the invention. As illustrated, the particles are substantially spherical, devoid any core and lack the surface graininess of the particles of FIG.


6


. The particles illustrated include a sulfur compound.





FIG. 9

illustrates a sodium bicarbonate granule granulated by practicing the technology set forth herein. Noteworthy is the spherical appearance and consolidation of the particle.




The inventive technology established herein affords a commercially viable and industrially significant development in the granulation art affording pellet content customization among other features.




Although embodiments of the invention have been described above, it is not limited thereto and it will be apparent to those skilled in the art that numerous modifications form part of the present invention insofar as they do not depart from the spirit, nature and scope of the claimed and described invention.



Claims
  • 1. A wet granulation method for granulating a feedstock into granules, comprising the steps of:providing a first feedstock having about 99.9% particle size of −150 mesh, of said 99.9% particle size of −150 mesh about 90% comprising a particle size of −200 mesh; providing a binder material having a moisture content; contacting said first feedstock with said binder; forming a pre-moistened mixture of said binder, said first feedstock and said moisture, said mixture having a moisture content of between 4% and 8% by weight; introducing said pre-moistened mixture onto a pan granulator containing second feedstock differently sized from said first feedstock in a size distribution of between −35 mesh and +150 mesh; maintaining moisture conditions on said pan where the moisture content on said pan is between 1.5% and 11% by weight; and forming first granules on said pan directly from contact of said pre-moistened mixture and said second feedstock in the absence of seed material.
  • 2. The method as set forth in claim 1, wherein said moisture content is between about 1.5% and about 10.5%.
  • 3. The method as set forth in claim 2, wherein said first moisture content is about 8%.
  • 4. The method as set forth in claim 1, wherein said first granules are in the size range of −10 mesh to 100 mesh.
  • 5. The method as set forth in claim 4, said method producing at least a 90% yield.
  • 6. The method as set forth in claim 1, wherein said feedstock is selected from the group comprising of sodium bicarbonate, potassium sulfate, potassium chloride, potassium nitrate, ammonium sulfate and sulfur.
  • 7. The method as set forth in claim 1, wherein said binder comprises about 60% moisture and about 40% solids.
  • 8. The method as set forth in claim 7, wherein between about 7% to about 9% by weight of said binder is added to said pan.
  • 9. The method as set fourth in claim 1, further including the step of adding an oil to formed first granules for dust control prior to further processing.
  • 10. The method as set forth in claim 9, wherein said oil comprises an oil selected from the group consisting of canola oil, vegetable oil, mineral oil.
  • 11. The method as set forth in claim 1, wherein said binder is dry, said pre-moistened mixture deriving moisture content from the addition of water.
  • 12. The method as set forth in claim 1, further including the step of treating said first granule in a second pan to form second granules from said first granules wherein said feedstock for said second pan includes between about 20% to about 35% product in the size range of −10 mesh to about 100 mesh.
  • 13. The method as set forth in claim 12, wherein said second granules from said second pan comprise granules in a size range from between −4 mesh and −8 mesh.
  • 14. A wet granulation method for granulating a feedstock into granules, comprising the steps of:providing a first feedstock having about 99.9% particle size of −150 mesh of said 99.9% particle size of −150 mesh about 90% comprising a particle size of −200 mesh; providing a binder material having a moisture content; contacting said first feedstock with said binder; forming a pre-moistened mixture of said binder, said first feedstock and said moisture, said mixture having a moisture content of between 4% and 8% by weight; introducing said pre-moistened mixture onto a pan granulator containing said first feedstock; maintaining pan moisture conditions where the moisture content on said pan is between 15% to about 11% by weight; forming first granules on said pan directly from contact of said pre-moistened mixture and said first feedstock in the absence of seed material; passing formed first granules onto a second pan granulator in the absence of said seed or nucleating material; and forming second granules in a different size distribution relative to said first granules.
US Referenced Citations (108)
Number Name Date Kind
2741545 Nielsson Apr 1956 A
3206297 O'Connor Sep 1965 A
3206528 Coombs et al. Sep 1965 A
3295950 Blouin et al. Jan 1967 A
3342578 Harshman et al. Sep 1967 A
3348938 Sherrington et al. Oct 1967 A
3360355 Horsley et al. Dec 1967 A
3408169 Thompson et al. Oct 1968 A
3423171 Hoppe et al. Jan 1969 A
3429657 George et al. Feb 1969 A
3436175 Atwood et al. Apr 1969 A
3449106 Paden et al. Jun 1969 A
3502458 Schenk Mar 1970 A
3527592 McPherson et al. Sep 1970 A
3528767 Garrett Sep 1970 A
3533776 Coates et al. Oct 1970 A
3536475 Trub Oct 1970 A
3539326 Otsuka et al. Nov 1970 A
3544296 Karcher Dec 1970 A
3567419 Dean et al. Mar 1971 A
3578399 Boeglin May 1971 A
3617237 Nagasawa et al. Nov 1971 A
3617243 Neitzel Nov 1971 A
3635691 Earl Jan 1972 A
3645714 Heming et al. Feb 1972 A
3656891 Chemtob Apr 1972 A
3687639 Barlow et al. Aug 1972 A
3711254 McGowan et al. Jan 1973 A
T909003 Hicks et al. Apr 1973 I4
3728438 Nasyrov Apr 1973 A
3785796 Mann, Jr. Jan 1974 A
3808051 Schoenholz et al. Apr 1974 A
3843772 Boeglin Oct 1974 A
3853490 Boeglin et al. Dec 1974 A
3892552 Gay, Jr. Jul 1975 A
3923489 Richardosn Dec 1975 A
3928015 Siegel et al. Dec 1975 A
3940257 Sherwin et al. Feb 1976 A
3967930 Sadan Jul 1976 A
3983211 Nasyrov et al. Sep 1976 A
3984521 Nasyrov et al. Oct 1976 A
3998935 Adams et al. Dec 1976 A
4034120 Wortham et al. Jul 1977 A
4045543 Sardisco Aug 1977 A
4116848 Schoenholz et al. Sep 1978 A
4129642 Neitzel Dec 1978 A
4131668 Sasaki et al. Dec 1978 A
4142885 Heumann et al. Mar 1979 A
4174382 Menche Nov 1979 A
4175943 Jordaan et al. Nov 1979 A
4183738 Carmon Jan 1980 A
4215100 Sokolov et al. Jul 1980 A
4264543 Valenta Apr 1981 A
4268492 Sardisco et al. May 1981 A
4303619 Kobayashi et al. Dec 1981 A
4323386 Heggebo et al. Apr 1982 A
4330319 Bexton et al. May 1982 A
4334906 Young Jun 1982 A
4342737 Iwashita et al. Aug 1982 A
4344747 Henry Aug 1982 A
4353852 Tse Oct 1982 A
4371481 Pollock Feb 1983 A
4371512 Sardisco et al. Feb 1983 A
4385920 Dancy et al. May 1983 A
4420468 Yamashita et al. Dec 1983 A
4436710 Miyazaki et al. Mar 1984 A
4451439 Maurel et al. May 1984 A
4528039 Rubin et al. Jul 1985 A
4533536 Bichara et al. Aug 1985 A
4554004 Bierman et al. Nov 1985 A
4554151 Worthington et al. Nov 1985 A
4562058 Dancy et al. Dec 1985 A
4588573 Worthington et al. May 1986 A
4589904 Harrison et al. May 1986 A
4610715 Monaldi et al. Sep 1986 A
4668242 Vitellaro et al. May 1987 A
4707347 Vajna et al. Nov 1987 A
4743287 Robinson May 1988 A
4842790 Nunnelly Jun 1989 A
4943308 Vanmarcke et al. Jul 1990 A
5019564 Lowe et al. May 1991 A
5043007 Davis Aug 1991 A
5108481 Shutt Apr 1992 A
5112379 Young May 1992 A
5124104 Holley Jun 1992 A
H1070 Harrison et al. Jul 1992 H
5152821 Walter Oct 1992 A
5177008 Kampen Jan 1993 A
5177009 Kampen Jan 1993 A
5264017 Van de Walle Nov 1993 A
5298050 McLaughlin et al. Mar 1994 A
5322532 Kurtz Jun 1994 A
5330552 Rizzo Jul 1994 A
5352265 Weston et al. Oct 1994 A
5366534 Fischbein et al. Nov 1994 A
5378259 Bassetti et al. Jan 1995 A
5383951 Cross et al. Jan 1995 A
5433766 Ming et al. Jul 1995 A
5460765 Derdall et al. Oct 1995 A
5529764 Lampert et al. Jun 1996 A
5549876 Zisner et al. Aug 1996 A
5552126 Efraim et al. Sep 1996 A
5571303 Bexton Nov 1996 A
5599373 Zanuccoli Feb 1997 A
5624649 Gal Apr 1997 A
5725630 Roberts et al. Mar 1998 A
5849060 Diping et al. Dec 1998 A
6013216 Watanabe et al. Jan 2000 A
Foreign Referenced Citations (6)
Number Date Country
2214145 Mar 1996 CA
2151569 Dec 1996 CA
0 289 074 Nov 1988 EP
0 748 651 Dec 1996 EP
1383110 Feb 1975 GB
WO 9739826 Oct 1997 WO
Non-Patent Literature Citations (1)
Entry
“Advanced Fertilizer and Industrial Mineral Technology”, Solterra Minerals, Inc.