WO2022011268A1 - Potassium humate zinc sulfate compound - Google Patents

Potassium humate zinc sulfate compound Download PDF

Info

Publication number
WO2022011268A1
WO2022011268A1 PCT/US2021/041100 US2021041100W WO2022011268A1 WO 2022011268 A1 WO2022011268 A1 WO 2022011268A1 US 2021041100 W US2021041100 W US 2021041100W WO 2022011268 A1 WO2022011268 A1 WO 2022011268A1
Authority
WO
WIPO (PCT)
Prior art keywords
zinc sulfate
potassium humate
sulfate compound
further example
making
Prior art date
Application number
PCT/US2021/041100
Other languages
French (fr)
Inventor
Kevin Merritt
Original Assignee
Kevin Merritt
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from US16/924,856 external-priority patent/US11691999B2/en
Application filed by Kevin Merritt filed Critical Kevin Merritt
Priority to CA3185134A priority Critical patent/CA3185134A1/en
Priority to MX2023000422A priority patent/MX2023000422A/en
Publication of WO2022011268A1 publication Critical patent/WO2022011268A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05DINORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C; FERTILISERS PRODUCING CARBON DIOXIDE
    • C05D1/00Fertilisers containing potassium

Definitions

  • a process such as is described in various embodiments herein relates to making a potassium hum ate zinc sulfate compound.
  • a potassium hum ate zinc sulfate compound may be used in a liquid, powder, or granule form and is useful as an organic aid to crop growth as well as useful for overcoming a plethora of soil problems.
  • humic substances include fulvic acid, humic acid, and/or huniin.
  • fulvic acid has the lowest molecular weight, and least resistance to decomposition by microorganisms; humin has the highest molecular weight and greatest resistance to decomposition, because it has a large number of negative charges per unit mass, humin also has a very high CEC.
  • the large molecules of humus bind to clay particles and greatly increase aggregate formation and stability therefore improving soil properties.
  • Humin is the alkali (and acid) insoluble portion of HS that many manufacturers dispose of, although it is known that there are individuals who may extract and use it.
  • a process for making a potassium humate zinc sulfate compound includes: obtaining a plurality of fully-soluble potassium humate powder particles; obtaining a zinc sulfate compound; and mixing the plurality of potassium humate particles with the zinc sulfate compound, thus forming a homogenized mixture; and thereby forming a potassium humate zinc sulfate compound configured to be applied to a soil surface.
  • the potassium humate zinc sulfate compound is a powder.
  • the potassium humate zinc sulfate compound is a granule and the process further includes: adding a binder to the homogenized mixture; and granulating the homogenized mixture into a granule, thus making a potassium humate zinc sulfate compound granule.
  • the binder is water. In some such instances, this granulating occurs at a temperature ranging between about 65 degrees Fahrenheit and about 190 degrees Fahrenheit .
  • obtaining the plurality of fully-soluble potassium humate powder particles further includes: obtaining a sample of a carbonaceous substance comprising humic acid and one or more other substances; contacting the sample with an amount of an alkaline mixture, thereby forming an extraction mixture, the extraction mixture consisting essentially of a sludge component; the sludge component comprising, predominantly, the sample, and an extraction component, the extraction component comprising, predominantly, the alkaline mixture; maintaining the sludge component in contact with the extraction component for a period of time sufficient for the extraction component to become relatively enriched in humic acid and the sludge component to become relatively depleted of humic acid; separating the sludge component from the extraction component; and spray drying the extraction component, thereby forming the plurality of potassium humate powder particles.
  • the zinc sulfate compound is a powder zinc sulfate.
  • the homogenized mixture includes about 5 pounds to about 500 pounds of the plurality of potassium humate powder particles to about 1,995 pounds to about 1,500 pounds of zinc sulfate.
  • the potassium humate zinc sulfate compound has a pH of 2 to about 12.
  • at least 95% of the plurality of potassium humate powder particles dissolve within five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius.
  • a process for making a potassium humate zinc sulfate compound includes: obtaining a plurality of potassium humate powder particles, where at least 95% of the plurality of potassium humate powder particles dissolve within five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius; obtaining a zinc sulfate compound; and mixing the plurality of potassium humate particles with the zinc sulfate, thereby forming a homogenized mixture; where the homogenized mixture includes about 5 pounds to about 500 pounds of the plurality of potassium humate powder particles to about 1,995 pounds to about 1,500 pounds of zinc sulfate compound; thereby forming a potassium humate zinc sulfate compound configured to be applied to a soil surface.
  • the potassium humate zinc sulfate compound is a powder.
  • the potassium humate zinc sulfate compound is a granule and the process further includes: adding a binder to the homogenized mixture; granulating the homogenized mixture into a granule, thereby making a potassium humate zinc sulfate compound granule.
  • the binder is water.
  • the granulating occurs at a temperature ranging between about 65 degrees Fahrenheit and about 190 degrees Fahrenheit.
  • the potassium humate zinc sulfate compound has a pH of 2 to about 12.
  • a potassium humate zinc sulfate compound includes: a powder potassium humate component, where at least 95% of the plurality of potassium humate powder particles dissolve within five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius; a zinc sulfate component; where the powder potassium humate component and the zinc sulfate component are homogenized at a ratio ranging between about 1:399 to and about 1:3; where the potassium humate zinc sulfate compound has a pH of 2 to about 12.
  • the potassium humate zinc sulfate compound is a powder configured to be applied to a soil surface.
  • FIGURE 1 is a flowchart illustrating an example sequence of operations for manufacturing a potassium humate zinc sulfate compound consistent with some embodiments described herein.
  • FIGURES 2A-B are photographic illustrations of potassium humate zinc sulfate granules consistent with some embodiments described herein.
  • FIGURE 2A illustrates potassium humate zinc sulfate granules about 0.8 mm to about 1.99 mm in diameter
  • FIGURE 2B illustrates potassium humate zinc sulfate granules about 2.0 to about 4.0 mm in diameter.
  • FIGURES 2A-2B include a United States penny for reference, which has a standard diameter of 19.05 mm.
  • DETAILED DESCRIPTION [0019] A process and composition such as is described in various embodiments herein now will be described more fully hereinafter. A process such as is described in various embodiments herein may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of a process such as is described in various embodiments herein to those skilled in the art. As used in this specification and the claims, the singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise.
  • a product is “enriched in humic acid” if the product possesses a higher concentration of humic acid than a raw material from which the product is made.
  • a component becomes “enriched in humic acid” as the concentration of humic acid in the component increases.
  • a component becomes “depleted of humic acid” as the concentration of humic acid in the component decreases.
  • a “carbonaceous substance comprising humic acid and one or more other substances” refers to a carbonaceous substance that contains humic acid and that also contains one or more other substances other than humic acid.
  • An example is Humalite.
  • An example is lignite.
  • An example is Leonardite.
  • humate refers to a fully- water soluble humic acid composition in the form of a salt.
  • potassium humate is a fully-water soluble potassium salt of humic acid
  • ammonium humate is a fully-water soluble ammonium salt of humic acid, and so on.
  • a method of making a potassium humate zinc sulfate compound 100 is illustrated a multi-step process. This process includes, at block 105, obtaining the raw materials for making the potassium humate powder, and then, at block 110, manufacturing the potassium humate powder.
  • the manufacturing includes blending of raw material and an alkaline mixture in a blend tank; screening of the blended mixture that was made in the blend tank; and drying of the liquid derived from screening of the blended mixture, thereby forming a fine potassium humate powder.
  • the zinc sulfate compound is made, which will be discussed in detailed herein.
  • the fine potassium humate powder is added to the zinc sulfate compound, forming a homogenized mixture, the homogenized mixture thereby forming the potassium humate zinc sulfate compound.
  • This compound may then be packaged into one of two forms: (1) packaged for use in a powder form (block 150); or (2) formed into granules (block 155) and packaged for use in granule form (block 160).
  • the manufacturing of the potassium humate powder includes, in an example, a blending of raw material with an alkaline mixture in a blend tank resulted in extraction of humic acid and other humic substances from the raw material.
  • Hot water and caustic potash solution and Humalite were added to a thermally insulated tank in that order and blended. The hot water was at 160-180 degrees Fahrenheit. The caustic potash solution was 45% membrane grade.
  • the mass ratio of hot water to caustic potash solution to humalite was 73.7:5.8:20.5.
  • water, caustic potash solution and Humalite were placed into a thermally insulated tank to form a 42,000 lb mixture, which was then blended.
  • the liquid phase was sampled, and a colorimetric assay for humic acid was performed on each sample, in which the amount of light absorbed was proportional to the concentration of humic acid.
  • a blended mixture prepared according to the paragraph immediately above consisted of liquid and sludge. This blended mixture was then pumped by a 3 HP motor to two 200 mesh screeners at a rate of ⁇ 40 gal/min ( ⁇ 350 lbs/min).
  • the screener allowed liquids and very small particles to be passed through, but not the insoluble sand, clay, and humin fraction, also known as sludge.
  • the amount of sludge varied, but typically the sludge was about 5-7% of the total weight of the blended mixture.
  • the screened humic acid enriched liquid which had a density of 8.35-9 lb/gallon, was collected in an insulation tank, which had a capacity of 12500 gal.
  • the humic acid enriched liquid was pumped from the insulation tank to a spray dryer firing tank from which it was transferred to a spray dryer.
  • a spray dryer system comprised a burner, a dryer, two cyclone separators, a baghouse and a powder hopper.
  • Humic acid enriched liquid was processed at a rate of 14-16 gal/min. Hydraulic pressure-nozzle atomization was used in which liquid was passed through a filter and then through a hydraulic pressure pump. The pressure of the liquid was directly proportional to the force delivered by the hydraulic pressure pump and was generally 1500 psi but ranged from 1300-1700 psi depending on the moisture of the fine powder.
  • the humic acid enriched liquid was then forced through 8 nozzles to break the liquid into fine droplets. Filtered air was passed through a burner where it was heated to 600- 650 degrees Fahrenheit.
  • the temperature of the inlet air never exceeded 800 degrees Fahrenheit.
  • the hot air met the liquid droplets in a co-current manner for a time of about 2 seconds. This time was enough to remove more than 85% of the moisture from the dryer to form a humic acid enriched powder, which was collected in a common line.
  • the air emerging out of the dryer still had some particles and was generally at 190-205 degrees Fahrenheit and never exceeded 250 degrees Fahrenheit. Heavier particles were collected using two cyclone separators in series and the lighter particles were collected using a baghouse filter.
  • the hot gas also called flue gas, was then emitted from the bag house; the hot gas consisted mostly of air and steam at 150-180 degrees Fahrenheit. The temperature of the exhaust never exceeded 250 degrees Fahrenheit.
  • the potassium humate or humic acid enriched powder from the common line was then transferred to a powder hopper.
  • Moisture content of the powder was measured and kept between 11%-13%.
  • moisture content was increased in either of two ways, by reducing the temperature of the burner or by operating the hydraulic pressure pump at a higher capacity which in turn increased the flow rate of the liquid.
  • moisture content was decreased in either of two ways, by increasing the temperature of the burner or by operating the hydraulic pressure pump at a lower capacity which in turn decreased the flow rate of the liquid.
  • the loose bulk density of the potassium humate powder ranged from about 35 to about 42 pounds per cubic foot.
  • the feed particle size distribution of a typical powder sample was as follows: 1.5% of the particles by weight were less than 100 microns; 15% of the particles by weight were less than 200 microns; 35% of the particles by weight were less than 270 microns; 55% of the particles by weight were less than 400 microns.
  • This fine, fully soluble potassium humate powder may be combined with zinc sulfate to form the potassium humate zinc sulfate compound.
  • the zinc sulfate utilized herein may be, in some instances, formed by obtaining the necessary raw materials (block 115), including zinc oxide and sulfuric acid. At block 120, these raw materials may be mixed in a reactor tank also containing sodium carbonate and water in order to purify the raw materials.
  • the mixture goes through a leaching process.
  • the mixture is filtered and a brine results.
  • This brine may then go through a water treatment process.
  • a “cake”, a solidified or semi-solidified sediment, may results from the water treatment process, this “cake” may then be added to a counter current washing process.
  • the zinc-rich materials obtained may then be reacted with sulfuric acid.
  • the result of this chemical reaction is passed through a filter press, which retains all non-leachable solids, resulting in a zinc sulfate solution free of particles.
  • zinc sulfate solution now free of particles, goes through a further purification process, in which zinc dust is added to perform an ion exchange between the zinc, lead and cadmium contents in the solution.
  • the heavy metal-free solution is then filtered through a filter press to retain all the solid precipitates.
  • the resulting zinc sulfate solution may be dried, either by the spray drying into powders an/or granulated using a fluid bed dryer. During the drying process, regardless of whether a powder or granule is formed, the purified solution is in contact with combustion gases generated from natural gas burning, and as a result water is evaporated.
  • the resulting product is a salt of zinc sulfate monohydrate.
  • the process for manufacturing the zinc sulfate may occur at elevated temperatures, for example about 800 degrees Fahrenheit. Such elevated temperatures may denature the active components of the potassium humate, and accordingly the zinc sulfate and potassium humate powder may require mixing at a lower temperature (block 145). For example, this mixing and subsequent granulation (if occurring) may be about 65 degrees Fahrenheit to about 190 degrees Fahrenheit.
  • the potassium humate zinc sulfate compound may be manufactured using a batch or a continuous flow method depending on the manufacturing set up and/or product demand needs.
  • the potassium humate zinc sulfate compound powder may then be packaged (block 150) and applied to a soil.
  • the potassium humate zinc sulfate compound may be granulated (block 155), as will be discussed in detail herein, and used in the form of granules. In a non-limiting example, this granulation may be done via a rotary pelletizing cone. In such instances, water may be added as a binding agent.
  • binders may include, but are not limited to, lingo sulfanate, mineral oil, vegetable oil, or the like.
  • the powder rotates in the pelletizer and agglomerates into substantially round granules.
  • the resulting granules may then be packaged (block 160) and applied to a soil.
  • the resulting potassium humate zinc sulfate compound powder or granule compound has been found to aid plant growth in both agricultural and horticultural applications.
  • soil organic matter may hold zinc in a chelated form; chelation is the process of holding or binding of a metal (e.g. zinc) to a large organic molecule.
  • the potassium humate zinc sulfate compound may for example, in calcareous soils, may cause fixed calcium carbonates and free lime to release calcium in soil solution, while the potassium humate (soluble humic acid) may alter the rhizodeposition and plant roots. This may result in a metamorphosis of overall root architecture, provide more root hair, and translocate the exchangeable calcium to the plant roots and plant tissues.
  • the potassium humate also may simultaneously buffer, chelate, and complex macro-micronutrients, making them more readily available to roots and plants. Furthermore, due to its nanoparticle size the potassium humate (soluble humic acid) may create micropores for roots, water, and nutrients to reside, which may become oxygenated as a result of the dynamics of soil physics.
  • a process for making a potassium humate zinc sulfate compound comprising: obtaining a plurality of fully-soluble potassium humate powder particles; obtaining a zinc sulfate compound; and mixing the plurality of potassium humate particles with the zinc sulfate, thereby forming a homogenized mixture; thereby forming a potassium humate zinc sulfate compound configured to be applied to a soil surface.
  • the binder is water.
  • obtaining the plurality of fully-soluble potassium humate powder particles further includes: obtaining a sample of a carbonaceous substance comprising humic acid and one or more other substances; contacting the sample with an amount of an alkaline mixture, thereby forming an extraction mixture, the extraction mixture consisting essentially of a sludge component; the sludge component comprising, predominantly, the sample, and an extraction component, the extraction component comprising, predominantly, the alkaline mixture; maintaining the sludge component in contact with the extraction component for a period of time sufficient for the extraction component to become relatively enriched in humic acid and the sludge component to become relatively depleted of humic acid; separating the sludge component from the extraction component; and spray drying the extraction component, thereby forming the plurality of potassium humate powder particles.
  • a process according to further example 6, wherein the alkaline mixture comprises sodium hydroxide or potassium hydroxide. [0047] Further example 13. A process according to further example 6, wherein the alkaline mixture comprises caustic potash solution. [0048] Further example 14. A process according to further example 6, wherein the alkaline mixture comprises, by mass, between about 10 and about 15 parts water, and about 1 part caustic potash solution, wherein the caustic potash solution is 45% membrane grade. [0049] Further example 15. A process according to further example 6, wherein the alkaline mixture comprises, by mass, about 73.7 parts water and about 5.8 parts caustic potash solution, wherein the caustic potash solution is 45% membrane grade. [0050] Further example 16.
  • a process according to further example 6, wherein the mass ratio of the alkaline mixture to the sample is between about 75:25 and about 84:16. [0051] Further example 17. A process according to further example 6, wherein the mass ratio of the alkaline mixture to the sample is between about 78:22 and about 81:13. [0052] Further example 18. A process according to further example 6, wherein the mass ratio of the alkaline mixture to the sample is about 79.5:20.5. [0053] Further example 19. A process according to further example 6, wherein the sludge component is maintained in contact with the extraction component for between about 4 hours and about 12 hours. [0054] Further example 20.
  • Further example 21 A process according to further example 6, wherein the sludge component is maintained in contact with the extraction component for about 8 hours.
  • Further example 22 A process according to further example 6, wherein the sludge component is maintained in contact with the extraction component for a period of time sufficient for the extraction component to possess a humic acid content of at least about 6%.
  • Further example 23 A process according to further example 6, wherein the sludge component is maintained in contact with the extraction component for a period of time sufficient for the extraction component to possess a humic acid content of at least about 14%.
  • Further example 29 A process according to further example 6, wherein the drying is effected by spray drying, and wherein the spray drying is characterized by an inlet temperature and an outlet temperature, and wherein the inlet temperature passing through a burner heats to between about 400 degrees Fahrenheit and about 800 degrees Fahrenheit, and wherein the outlet temperature is between bout 150 degrees Fahrenheit and about 250 degrees Fahrenheit.
  • a process according to further example 6, wherein the plurality of powder particles is characterized by a moisture content, and wherein the moisture content is between about 10% and about 14%.
  • a process according to further example 6, wherein the plurality of powder particles is characterized by a moisture content, and wherein the moisture content is between about 11% and about 13%.
  • Further example 34 A process according to further example 6, wherein the plurality of powder particles is characterized by a loose bulk density, and wherein the loose bulk density is between about 28 and about 49 pounds per cubic foot.
  • Further example 35 A process according to further example 6, wherein the plurality of powder particles is characterized by a loose bulk density, and wherein the loose bulk density is between about 31.5 and about 45.5 pounds per cubic foot.
  • Further example 36 Further example 36.
  • Further example 37. A process according to further example 6, wherein the plurality of powder particles is characterized by a particle size distribution, and wherein, in the particle size distribution, about 1.5% of the particles by weight are less than about 100 microns, about 15% of the particles by weight are less than about 200 microns, about 35% of the particles by weight are less than 270 microns, and about 55% of the particles by weight are less than about 400 microns.
  • Further example 39. A process according to further example 1, wherein at least about 90% of the plurality of potassium humate particles are dissolved in five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius.
  • Further example 40. A process according to further example 1, wherein at least about 95% of the plurality of potassium humate particles are dissolved in five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius.
  • Further example 42. A process according to further example 1, wherein 100% of the plurality of potassium humate particles are dissolved in five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius.
  • Further example 43. A process according to further example 1, wherein at least about 75% of the plurality of potassium humate particles are dissolved in one minute when submerged in one liter of water at a temperature of 25 degrees Celsius.
  • Further example 45 A process according to further example 1, wherein at least about 95% of the plurality of potassium humate particles are dissolved in one minute when submerged in one liter of water at a temperature of 25 degrees Celsius.
  • Further example 46 A process according to further example 1, wherein at least about 99% of the plurality of potassium humate particles are dissolved in one minute when submerged in one liter of water at a temperature of 25 degrees Celsius.
  • obtaining zinc sulfate includes obtaining a commercially available zinc sulfate composition.
  • a process according to further example 1, wherein obtaining zinc sulfate further includes: obtaining raw materials, including zinc oxide and sulfuric acid; mixing the zinc oxide and the sulfuric acid with water and sodium carbonate, thereby forming a zinc sulfate solution; leaching the zinc sulfate solution, thereby forming a leached zinc sulfate solution; purifying the leached zinc sulfate solution, thereby forming a purified zinc sulfate solution; and filtering the purified zinc sulfate solution through a filter press, retaining all solid precipitates and thereby forming a final zinc sulfate solution.
  • a process according to further example 49 wherein mixing the zinc oxide and the sulfuric acid with water and sodium carbonate occurs at about 60 degrees Celsius to about 65 degrees Celsius.
  • Further example 51 A process according to further example 49, wherein the zinc oxide, sulfuric acid, water, and sodium carbonate are mixed for approximately 8 hours.
  • leaching the zinc sulfate solution additionally includes filtering the zinc sulfate solution, resulting in a brine; subjecting the brine through a water treatment process, resulting in a “cake”, or solidified or semi-solidified sediment.
  • a process according to further example 49, wherein purifying the leached zinc sulfate solution includes adding zinc dust to the leached zin sulfate to perform an ion exchange between the zinc, lead and cadmium contents in the solution.
  • purifying the leached zinc sulfate solution occurs at a temperature of about 70 degrees Celsius to about 80 degrees Celsius.
  • Further example 56 A process according to further example 49, further includes drying the final zinc sulfate solution for about 15 minutes at about 550 degrees Celsius in order to form zinc sulfate powder.
  • Further example 57 Further example 57.
  • Further example 59. A process according to further example 57, wherein the flat surface is a steel belt.
  • Further example 60 A process according to further example 59, wherein the solidifying further includes cooling the mixture on the flat surface.
  • the cooling is effectuated by spraying a cooled liquid solution (e.g., 40 to 50 degrees Fahrenheit), for example water, on the underside of the steel belt, resulting in the cooling of the belt and subsequently the homogenized mixture deposited thereon.
  • a cooled liquid solution e.g. 40 to 50 degrees Fahrenheit
  • the cooling is effectuated by moving the belt into, or through, a chiller. In some instances, such a chiller may be set to about 40 to 50 degrees Fahrenheit, although this is not to be understood as limiting.
  • Further example 63 A process according to further example 60, wherein the cooling may be any other active means of cooling known in the art, such as other forms of refrigeration or freezing.
  • Further example 64 A process according to further example 60, wherein the cooling may be a passive means of cooling; for example the cooling may be simply allowing the mixture to cool to room temperature without any further intervention.
  • Further example 65 A process according to further example 57, wherein the process further includes passing the resulting granules through a sized screen to produce a desired granule size.
  • Further example 66 A process according to further example 57, wherein the potassium humate zinc sulfate compound granule is between about 0.5 mm and about 5.0 mm.
  • Further example 67 A process according to further example 57, wherein the potassium humate zinc sulfate compound granule is between about 0.8 mm and about 4.0 mm.
  • Further example 68 A process according to further example 57, wherein the potassium humate zinc sulfate compound granule is between about 0.8 mm and about 1.99 mm.
  • Further example 69 A process according to further example 1, wherein the potassium humate zinc sulfate compound granule is between about 2.0 mm and about 4.0 mm.
  • Further example 70 A process according to further example 1, wherein the potassium humate zinc sulfate compound granule has a pH of at least 2.
  • Further example 71 A process according to further example 1, wherein the potassium humate zinc sulfate compound granule has a pH of 2 to about 12.
  • Further example 72 A process according to further example 1, wherein the potassium humate zinc sulfate compound granule has a pH of about 7.
  • Further example 73 A process according to further example 1, wherein the process further includes applying the potassium humate zinc sulfate compound to a desired site, such as an agriculture setting.
  • a potassium humate zinc sulfate compound the compound made by a process comprising: obtaining a plurality of fully-soluble potassium humate powder particles; obtaining a zinc sulfate compound; and mixing the plurality of potassium humate particles with the zinc sulfate, thereby forming a homogenized mixture; thereby forming a potassium humate zinc sulfate compound configured to be applied to a soil surface.
  • a potassium humate zinc sulfate compound comprising: a powder potassium humate component, wherein at least 95% of the plurality of potassium humate powder particles dissolve within five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius; a zinc sulfate component; wherein the powder potassium humate component and the zinc sulfate are homogenized at a ratio ranging between about 1:399 to and about 1:3; wherein the potassium humate zinc sulfate compound has a pH of 2 to about 12.
  • Further example 76. A potassium humate zinc sulfate compound according to further example 75, wherein the potassium humate zinc sulfate compound is a powder.
  • Further example 78. A potassium humate zinc sulfate compound according to further example 77, wherein the potassium humate zinc sulfate compound granule is between about 0.5 mm and about 5.0 mm.
  • Further example 79. A potassium humate zinc sulfate compound according to further example 77, wherein the potassium humate zinc sulfate compound granule is between about 0.8 mm and about 4.0 mm.
  • a potassium humate zinc sulfate compound according to further example 77 wherein the potassium humate zinc sulfate compound granule is between about 0.8 mm and about 1.99 mm.
  • Further example 81 A potassium humate zinc sulfate compound according to further example 77, wherein the potassium humate zinc sulfate compound granule is between about 2.0 mm and about 4.0 mm.
  • Further example 82 A potassium humate zinc sulfate compound according to further example 75, wherein the potassium humate zinc sulfate compound is configured to be applied to a desired location.
  • Further example 83 Further example 83.
  • Further example 84. A potassium humate zinc sulfate compound according to further example 82, wherein the potassium humate zinc sulfate compound granules between about 2.0 mm and about 4.0 mm may be applied to agricultural soils.
  • Further example 85. A potassium humate zinc sulfate compound according to further example 82, wherein the potassium humate zinc sulfate compound granules between about 0.8 mm and about 1.99 mm may be applied to turf soils.
  • the granules may generally vary in shape and size, and in some instances varying sizes and shapes may be utilized for different purposes.
  • smaller composite granules e.g. about 0.8 to about 1.99 mm in diameter
  • turf applications e.g. on golf courses, lawn maintenance, etc.
  • larger granules e.g. about 2.0 to about 4.0 mm in diameter
  • such as those illustrated in Figure 2B may be utilized in agricultural applications.
  • FIG. 87 A plurality of potassium humate zinc sulfate granules according to further example 86 were subjected to crush strength testing. The composite granules were separated by size, with potassium humate zinc sulfate granules ranging from about 0.8 to 1.99 mm in diameter being tested together and potassium humate zinc sulfate granules ranging from about 2.0 to about 4 mm in diameter being tested together. Crush strength testing was conducted for granules ranging from about 0.8 to 1.99 mm in diameter and for granules ranging from about 2.0 to about 4.0 mm in diameter, respectively.
  • SGN Size Guide Number
  • the crush strength measurements of the granules ranging from about 0.8 to 1.99 mm in diameter range from about 6.5 psi to about 8.0 psi.
  • the crush strength measurements of the granules ranging from about 2.0 to 4.0 mm in diameter range from about 3.5 psi to about 5.0 psi.
  • these examples are for illustrative purposes only and are non-limiting, in some instances the crush strength of a granule consistent with the description herein may range anywhere from 0.1 psi to 10 psi.

Abstract

A process for making a potassium humate zinc sulfate compound, the process including: obtaining a plurality of fully-soluble potassium humate powder particles; obtaining a zinc sulfate compound; and mixing the plurality of potassium humate particles with the zinc sulfate compound, thereby forming a homogenized mixture, thereby forming a potassium humate zinc sulfate compound configured to be applied to a soil surface.

Description

POTASSIUM HUMATE ZINC SULFATE COMPOUND
FIELD OF THE INVENTION
[0001] A process such as is described in various embodiments herein relates to making a potassium hum ate zinc sulfate compound. Such a compound may be used in a liquid, powder, or granule form and is useful as an organic aid to crop growth as well as useful for overcoming a plethora of soil problems.
BACKGROUND OF THE INVENTION
[0002] It is known that humic substances (HS) include fulvic acid, humic acid, and/or huniin. Of these, fulvic acid has the lowest molecular weight, and least resistance to decomposition by microorganisms; humin has the highest molecular weight and greatest resistance to decomposition, because it has a large number of negative charges per unit mass, humin also has a very high CEC. The large molecules of humus bind to clay particles and greatly increase aggregate formation and stability therefore improving soil properties. Humin is the alkali (and acid) insoluble portion of HS that many manufacturers dispose of, although it is known that there are individuals who may extract and use it.
[0003] Since it takes longer for dry lignite to be broken down, and thus be functional in the soil, it is necessary to convert the lignite into forms that provide a more timely overall benefit (e.g. transformation into a water-soluble form). Such a conversion “unrolls” the tight molecular ball of lignite and creates water-soluble humic acids, either as a liquid or in the form of sodium, potassium, or ammonium salts (known as humates). Such a water-soluble form is desirable, as in their soluble form, humic acids can readily chelate nutrients, preserve nitrates from leaching, enhance root development, and improve overall crop vigor and yields. [0004] It is also known that there are numerous nutrients beneficial for soil growth that may not be present in large enough quantities or in a usable form in the soil. For example, a zinc deficiency may present in the form of stunted plants with small, yellowed, and/or deformed leaves. Zinc may often be present in soil organic matter in a chelated form. Chelation is the process of holding or binding of a metal (e.g. zinc) to a large organic molecule. Due to being chelated to soil particles these nutrients (e.g. zinc) are not able to readily move through the soil, and as such they may not available to plants. [0005] With respect to sulfur in the soil, about 70% to about 90% of sulfur present in soil is conventionally in the form of organic matter. This sulfur, contained with the organic matter, must be converted to sulfate by soil bacteria in order to be usable by plants. Conventionally, this conversion is very inefficient, making only small amounts of sulfate available to plants. [0006] There exists a need in the art for a fusion compound combining the functional carbons of potassium humate with zinc sulfate in order to meet the complex needs of plants. SUMMARY OF EMBODIMENTS [0007] The present embodiments provide one or more of the features recited in the appended claims and/or the following features which alone or in combination, may comprise patentable subject matter. [0008] In a first aspect, a process for making a potassium humate zinc sulfate compound includes: obtaining a plurality of fully-soluble potassium humate powder particles; obtaining a zinc sulfate compound; and mixing the plurality of potassium humate particles with the zinc sulfate compound, thus forming a homogenized mixture; and thereby forming a potassium humate zinc sulfate compound configured to be applied to a soil surface. [0009] In some embodiments, the potassium humate zinc sulfate compound is a powder. In other embodiments, the potassium humate zinc sulfate compound is a granule and the process further includes: adding a binder to the homogenized mixture; and granulating the homogenized mixture into a granule, thus making a potassium humate zinc sulfate compound granule. In some such instances, the binder is water. In some such instances, this granulating occurs at a temperature ranging between about 65 degrees Fahrenheit and about 190 degrees Fahrenheit . [0010] In some embodiments, obtaining the plurality of fully-soluble potassium humate powder particles further includes: obtaining a sample of a carbonaceous substance comprising humic acid and one or more other substances; contacting the sample with an amount of an alkaline mixture, thereby forming an extraction mixture, the extraction mixture consisting essentially of a sludge component; the sludge component comprising, predominantly, the sample, and an extraction component, the extraction component comprising, predominantly, the alkaline mixture; maintaining the sludge component in contact with the extraction component for a period of time sufficient for the extraction component to become relatively enriched in humic acid and the sludge component to become relatively depleted of humic acid; separating the sludge component from the extraction component; and spray drying the extraction component, thereby forming the plurality of potassium humate powder particles. [0011] In some embodiments, the zinc sulfate compound is a powder zinc sulfate. [0012] In some embodiments, the homogenized mixture includes about 5 pounds to about 500 pounds of the plurality of potassium humate powder particles to about 1,995 pounds to about 1,500 pounds of zinc sulfate. In other embodiments, the potassium humate zinc sulfate compound has a pH of 2 to about 12. In still other embodiments, at least 95% of the plurality of potassium humate powder particles dissolve within five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius. [0013] In another aspect, a process for making a potassium humate zinc sulfate compound includes: obtaining a plurality of potassium humate powder particles, where at least 95% of the plurality of potassium humate powder particles dissolve within five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius; obtaining a zinc sulfate compound; and mixing the plurality of potassium humate particles with the zinc sulfate, thereby forming a homogenized mixture; where the homogenized mixture includes about 5 pounds to about 500 pounds of the plurality of potassium humate powder particles to about 1,995 pounds to about 1,500 pounds of zinc sulfate compound; thereby forming a potassium humate zinc sulfate compound configured to be applied to a soil surface. [0014] In some embodiments, the potassium humate zinc sulfate compound is a powder. In other embodiments, the potassium humate zinc sulfate compound is a granule and the process further includes: adding a binder to the homogenized mixture; granulating the homogenized mixture into a granule, thereby making a potassium humate zinc sulfate compound granule. In some such embodiments, the binder is water. In other such instances, the granulating occurs at a temperature ranging between about 65 degrees Fahrenheit and about 190 degrees Fahrenheit. In some instances, the potassium humate zinc sulfate compound has a pH of 2 to about 12. [0015] In still yet another aspect, a potassium humate zinc sulfate compound includes: a powder potassium humate component, where at least 95% of the plurality of potassium humate powder particles dissolve within five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius; a zinc sulfate component; where the powder potassium humate component and the zinc sulfate component are homogenized at a ratio ranging between about 1:399 to and about 1:3; where the potassium humate zinc sulfate compound has a pH of 2 to about 12. [0016] In some embodiments, the potassium humate zinc sulfate compound is a powder configured to be applied to a soil surface. In other instances, the potassium humate zinc sulfate compound is a granule. BRIEF DESCRIPTION OF THE FIGRUES [0017] FIGURE 1 is a flowchart illustrating an example sequence of operations for manufacturing a potassium humate zinc sulfate compound consistent with some embodiments described herein. [0018] FIGURES 2A-B are photographic illustrations of potassium humate zinc sulfate granules consistent with some embodiments described herein. FIGURE 2A illustrates potassium humate zinc sulfate granules about 0.8 mm to about 1.99 mm in diameter; FIGURE 2B illustrates potassium humate zinc sulfate granules about 2.0 to about 4.0 mm in diameter. Each of FIGURES 2A-2B include a United States penny for reference, which has a standard diameter of 19.05 mm. DETAILED DESCRIPTION [0019] A process and composition such as is described in various embodiments herein now will be described more fully hereinafter. A process such as is described in various embodiments herein may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of a process such as is described in various embodiments herein to those skilled in the art. As used in this specification and the claims, the singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise. When used in this specification and the claims as an adverb rather than a preposition, “about” means “approximately” and comprises the stated value and every value within 10% of that value; in other words, “about 100%” includes 90% and 110% and every value in between. [0020] When used in this specification and the claims, a product is “enriched in humic acid” if the product possesses a higher concentration of humic acid than a raw material from which the product is made. A component becomes “enriched in humic acid” as the concentration of humic acid in the component increases. A component becomes “depleted of humic acid” as the concentration of humic acid in the component decreases. [0021] When used in this specification and the claims, a “carbonaceous substance comprising humic acid and one or more other substances” refers to a carbonaceous substance that contains humic acid and that also contains one or more other substances other than humic acid. An example is Humalite. An example is lignite. An example is Leonardite. [0022] When used in this specification and the claims, “humate” refers to a fully- water soluble humic acid composition in the form of a salt. For example “potassium humate” is a fully-water soluble potassium salt of humic acid, “ammonium humate” is a fully-water soluble ammonium salt of humic acid, and so on. [0023] Aspects of a process such as is described in various embodiments herein are further illustrated by the following examples, which are set forth to illustrate certain aspects of a process such as is described in various embodiments herein and are not to be construed as limiting thereof. [0024] Referring now to Figure 1, in an example, a method of making a potassium humate zinc sulfate compound 100 is illustrated a multi-step process. This process includes, at block 105, obtaining the raw materials for making the potassium humate powder, and then, at block 110, manufacturing the potassium humate powder. The manufacturing, at block 110, includes blending of raw material and an alkaline mixture in a blend tank; screening of the blended mixture that was made in the blend tank; and drying of the liquid derived from screening of the blended mixture, thereby forming a fine potassium humate powder. At blocks 115-140, the zinc sulfate compound is made, which will be discussed in detailed herein. At block 145, the fine potassium humate powder is added to the zinc sulfate compound, forming a homogenized mixture, the homogenized mixture thereby forming the potassium humate zinc sulfate compound. This compound may then be packaged into one of two forms: (1) packaged for use in a powder form (block 150); or (2) formed into granules (block 155) and packaged for use in granule form (block 160). [0025] More specifically the manufacturing of the potassium humate powder includes, in an example, a blending of raw material with an alkaline mixture in a blend tank resulted in extraction of humic acid and other humic substances from the raw material. Hot water and caustic potash solution and Humalite were added to a thermally insulated tank in that order and blended. The hot water was at 160-180 degrees Fahrenheit. The caustic potash solution was 45% membrane grade. The mass ratio of hot water to caustic potash solution to humalite was 73.7:5.8:20.5. [0026] In an example, water, caustic potash solution and Humalite were placed into a thermally insulated tank to form a 42,000 lb mixture, which was then blended. The liquid phase was sampled, and a colorimetric assay for humic acid was performed on each sample, in which the amount of light absorbed was proportional to the concentration of humic acid. [0027] In an example, a blended mixture prepared according to the paragraph immediately above consisted of liquid and sludge. This blended mixture was then pumped by a 3 HP motor to two 200 mesh screeners at a rate of ~40 gal/min (~350 lbs/min). It took ~120 minutes to screen 42000 lbs. The screener allowed liquids and very small particles to be passed through, but not the insoluble sand, clay, and humin fraction, also known as sludge. The amount of sludge varied, but typically the sludge was about 5-7% of the total weight of the blended mixture. [0028] In an example, the screened humic acid enriched liquid, which had a density of 8.35-9 lb/gallon, was collected in an insulation tank, which had a capacity of 12500 gal. The humic acid enriched liquid was pumped from the insulation tank to a spray dryer firing tank from which it was transferred to a spray dryer. [0029] In an example, a spray dryer system comprised a burner, a dryer, two cyclone separators, a baghouse and a powder hopper. Humic acid enriched liquid was processed at a rate of 14-16 gal/min. Hydraulic pressure-nozzle atomization was used in which liquid was passed through a filter and then through a hydraulic pressure pump. The pressure of the liquid was directly proportional to the force delivered by the hydraulic pressure pump and was generally 1500 psi but ranged from 1300-1700 psi depending on the moisture of the fine powder. The humic acid enriched liquid was then forced through 8 nozzles to break the liquid into fine droplets. Filtered air was passed through a burner where it was heated to 600- 650 degrees Fahrenheit. The temperature of the inlet air never exceeded 800 degrees Fahrenheit. The hot air met the liquid droplets in a co-current manner for a time of about 2 seconds. This time was enough to remove more than 85% of the moisture from the dryer to form a humic acid enriched powder, which was collected in a common line. The air emerging out of the dryer still had some particles and was generally at 190-205 degrees Fahrenheit and never exceeded 250 degrees Fahrenheit. Heavier particles were collected using two cyclone separators in series and the lighter particles were collected using a baghouse filter. The hot gas, also called flue gas, was then emitted from the bag house; the hot gas consisted mostly of air and steam at 150-180 degrees Fahrenheit. The temperature of the exhaust never exceeded 250 degrees Fahrenheit. The potassium humate or humic acid enriched powder from the common line was then transferred to a powder hopper. Moisture content of the powder was measured and kept between 11%-13%. When the moisture was below 11%, moisture content was increased in either of two ways, by reducing the temperature of the burner or by operating the hydraulic pressure pump at a higher capacity which in turn increased the flow rate of the liquid. When the moisture was above 13%, moisture content was decreased in either of two ways, by increasing the temperature of the burner or by operating the hydraulic pressure pump at a lower capacity which in turn decreased the flow rate of the liquid. The loose bulk density of the potassium humate powder ranged from about 35 to about 42 pounds per cubic foot. The feed particle size distribution of a typical powder sample was as follows: 1.5% of the particles by weight were less than 100 microns; 15% of the particles by weight were less than 200 microns; 35% of the particles by weight were less than 270 microns; 55% of the particles by weight were less than 400 microns. This fine, fully soluble potassium humate powder may be combined with zinc sulfate to form the potassium humate zinc sulfate compound. [0030] The zinc sulfate utilized herein may be, in some instances, formed by obtaining the necessary raw materials (block 115), including zinc oxide and sulfuric acid. At block 120, these raw materials may be mixed in a reactor tank also containing sodium carbonate and water in order to purify the raw materials. At block 125, the mixture goes through a leaching process. During the leaching process, the mixture is filtered and a brine results. This brine may then go through a water treatment process. A “cake”, a solidified or semi-solidified sediment, may results from the water treatment process, this “cake” may then be added to a counter current washing process. Following the counter-washing the zinc-rich materials obtained may then be reacted with sulfuric acid. The result of this chemical reaction is passed through a filter press, which retains all non-leachable solids, resulting in a zinc sulfate solution free of particles. At block 130, zinc sulfate solution, now free of particles, goes through a further purification process, in which zinc dust is added to perform an ion exchange between the zinc, lead and cadmium contents in the solution. At block 135, the heavy metal-free solution is then filtered through a filter press to retain all the solid precipitates. Finally, at block 140, the resulting zinc sulfate solution may be dried, either by the spray drying into powders an/or granulated using a fluid bed dryer. During the drying process, regardless of whether a powder or granule is formed, the purified solution is in contact with combustion gases generated from natural gas burning, and as a result water is evaporated. The resulting product is a salt of zinc sulfate monohydrate. [0031] The process for manufacturing the zinc sulfate (blocks 115-140) may occur at elevated temperatures, for example about 800 degrees Fahrenheit. Such elevated temperatures may denature the active components of the potassium humate, and accordingly the zinc sulfate and potassium humate powder may require mixing at a lower temperature (block 145). For example, this mixing and subsequent granulation (if occurring) may be about 65 degrees Fahrenheit to about 190 degrees Fahrenheit. In an example, the potassium humate zinc sulfate compound may be manufactured using a batch or a continuous flow method depending on the manufacturing set up and/or product demand needs. In some instances, they are continuously mixed, for example by stirring or blending, until the zinc sulfate and potassium humate form one substantially homogenous mixture. In some instances, the potassium humate zinc sulfate compound powder may then be packaged (block 150) and applied to a soil. [0032] In still other embodiments, the potassium humate zinc sulfate compound may be granulated (block 155), as will be discussed in detail herein, and used in the form of granules. In a non-limiting example, this granulation may be done via a rotary pelletizing cone. In such instances, water may be added as a binding agent. Other binders may include, but are not limited to, lingo sulfanate, mineral oil, vegetable oil, or the like. The powder rotates in the pelletizer and agglomerates into substantially round granules. The resulting granules may then be packaged (block 160) and applied to a soil. [0033] The resulting potassium humate zinc sulfate compound powder or granule compound has been found to aid plant growth in both agricultural and horticultural applications. Traditionally, soil organic matter may hold zinc in a chelated form; chelation is the process of holding or binding of a metal (e.g. zinc) to a large organic molecule. Due to the zinc being chelated to soil particles, it does not readily move through the soil, and thus is not available to plants. Additionally, about 70% to about 90% of sulfur present in soil is also conventionally in the form of organic matter, which must be converted to sulfate by soil bacteria in order to be usable by plants. Typically, various soil bacteria convert the zinc sulfate into the usable forms of zinc and sulfate; however, this process may be slow as the zinc sulfate may take a while to break down. The potassium humate zinc sulfate compound, may for example, in calcareous soils, may cause fixed calcium carbonates and free lime to release calcium in soil solution, while the potassium humate (soluble humic acid) may alter the rhizodeposition and plant roots. This may result in a metamorphosis of overall root architecture, provide more root hair, and translocate the exchangeable calcium to the plant roots and plant tissues. The potassium humate also may simultaneously buffer, chelate, and complex macro-micronutrients, making them more readily available to roots and plants. Furthermore, due to its nanoparticle size the potassium humate (soluble humic acid) may create micropores for roots, water, and nutrients to reside, which may become oxygenated as a result of the dynamics of soil physics. The combination of the potassium humate (soluble humic acid) and zinc sulfate may enhance the effect of conversion of zinc sulfate to a usable form of zinc. [0034] Aspects of a process such as is described in various embodiments herein are further illustrated by the following further examples, which are set forth to illustrate certain aspects of a process such as is described in various embodiments herein and are not to be construed as limiting thereof. [0035] Further example 1. A process for making a potassium humate zinc sulfate compound, the process comprising: obtaining a plurality of fully-soluble potassium humate powder particles; obtaining a zinc sulfate compound; and mixing the plurality of potassium humate particles with the zinc sulfate, thereby forming a homogenized mixture; thereby forming a potassium humate zinc sulfate compound configured to be applied to a soil surface. [0036] Further example 2. A process according to further example 1, wherein the potassium humate zinc sulfate compound is a powder. [0037] Further example 3. A process according to further example 1, wherein the potassium humate zinc sulfate compound is a granule, and the process further includes: adding a binder to the homogenized mixture; granulating the homogenized mixture into a granule, thereby making a potassium humate zinc sulfate compound granule. [0038] Further example 4. A process according to further example 3, wherein the binder is water. [0039] Further example 5. A process according to further example 3, wherein about 1 to about 25 gallons of binder are added per ton of homogenized powder. [0040] Further example 6. A process according to further example 1, wherein obtaining the plurality of fully-soluble potassium humate powder particles further includes: obtaining a sample of a carbonaceous substance comprising humic acid and one or more other substances; contacting the sample with an amount of an alkaline mixture, thereby forming an extraction mixture, the extraction mixture consisting essentially of a sludge component; the sludge component comprising, predominantly, the sample, and an extraction component, the extraction component comprising, predominantly, the alkaline mixture; maintaining the sludge component in contact with the extraction component for a period of time sufficient for the extraction component to become relatively enriched in humic acid and the sludge component to become relatively depleted of humic acid; separating the sludge component from the extraction component; and spray drying the extraction component, thereby forming the plurality of potassium humate powder particles. [0041] Further example 7. A process according to further example 6, wherein the carbonaceous substance comprises a coal and/or a claystone and/or a mudstone and/or a shale. [0042] Further example 8. A process according to further example 6, wherein the carbonaceous substance comprises a lignite and/or a Leonardite and/or a Humalite. [0043] Further example 9. A process according to further example 6, wherein the carbonaceous substance comprises a Humalite. [0044] Further example 10. A process according to further example 6, wherein the alkaline mixture comprises water. [0045] Further example 11. A process according to further example 6, wherein the alkaline mixture comprises a base. [0046] Further example 12. A process according to further example 6, wherein the alkaline mixture comprises sodium hydroxide or potassium hydroxide. [0047] Further example 13. A process according to further example 6, wherein the alkaline mixture comprises caustic potash solution. [0048] Further example 14. A process according to further example 6, wherein the alkaline mixture comprises, by mass, between about 10 and about 15 parts water, and about 1 part caustic potash solution, wherein the caustic potash solution is 45% membrane grade. [0049] Further example 15. A process according to further example 6, wherein the alkaline mixture comprises, by mass, about 73.7 parts water and about 5.8 parts caustic potash solution, wherein the caustic potash solution is 45% membrane grade. [0050] Further example 16. A process according to further example 6, wherein the mass ratio of the alkaline mixture to the sample is between about 75:25 and about 84:16. [0051] Further example 17. A process according to further example 6, wherein the mass ratio of the alkaline mixture to the sample is between about 78:22 and about 81:13. [0052] Further example 18. A process according to further example 6, wherein the mass ratio of the alkaline mixture to the sample is about 79.5:20.5. [0053] Further example 19. A process according to further example 6, wherein the sludge component is maintained in contact with the extraction component for between about 4 hours and about 12 hours. [0054] Further example 20. A process according to further example 6, wherein the sludge component is maintained in contact with the extraction component for between about 6 hours and about 10 hours. [0055] Further example 21. A process according to further example 6, wherein the sludge component is maintained in contact with the extraction component for about 8 hours. [0056] Further example 22. A process according to further example 6, wherein the sludge component is maintained in contact with the extraction component for a period of time sufficient for the extraction component to possess a humic acid content of at least about 6%. [0057] Further example 23. A process according to further example 6, wherein the sludge component is maintained in contact with the extraction component for a period of time sufficient for the extraction component to possess a humic acid content of at least about 14%. [0058] Further example 24. A process according to further example 6, wherein the sludge component is maintained in contact with the extraction component for a period of time sufficient for the extraction component to possess a humic acid content of at least about 17%. [0059] Further example 25. A process according to further example 6, wherein the sludge component is maintained in contact with the extraction component for a period of time sufficient for the extraction component to possess a humic acid content of at least about 18%. [0060] Further example 26. A process according to further example 6, wherein the separating is effected by filtration. [0061] Further example 27. A process according to further example 6, wherein the separating is effected by sedimentation. [0062] Further example 28. A process according to further example 6, wherein the drying is effected by spray drying. [0063] Further example 29. A process according to further example 6, wherein the drying is effected by spray drying, and wherein the spray drying is characterized by an inlet temperature and an outlet temperature, and wherein the inlet temperature passing through a burner heats to between about 400 degrees Fahrenheit and about 800 degrees Fahrenheit, and wherein the outlet temperature is between bout 150 degrees Fahrenheit and about 250 degrees Fahrenheit. [0064] Further example 30. A process according to further example 6, wherein the drying is effected by spray drying, and wherein the spray drying is characterized by an inlet temperature and an outlet temperature, and wherein the inlet temperature is between about 600 degrees Fahrenheit and about 650 degrees Fahrenheit, and wherein the outlet temperature is between about 150 degrees Fahrenheit and about 180 degrees Fahrenheit. [0065] Further example 31. A process according to further example 6, wherein the plurality of powder particles is characterized by a moisture content, and wherein the moisture content is between about 9% and about 15%. [0066] Further example 32. A process according to further example 6, wherein the plurality of powder particles is characterized by a moisture content, and wherein the moisture content is between about 10% and about 14%. [0067] Further example 33. A process according to further example 6, wherein the plurality of powder particles is characterized by a moisture content, and wherein the moisture content is between about 11% and about 13%. [0068] Further example 34. A process according to further example 6, wherein the plurality of powder particles is characterized by a loose bulk density, and wherein the loose bulk density is between about 28 and about 49 pounds per cubic foot. [0069] Further example 35. A process according to further example 6, wherein the plurality of powder particles is characterized by a loose bulk density, and wherein the loose bulk density is between about 31.5 and about 45.5 pounds per cubic foot. [0070] Further example 36. A process according to further example 6, wherein the plurality of powder particles is characterized by a loose bulk density, and wherein the loose bulk density is between about 35 and about 42 pounds per cubic foot. [0071] Further example 37. A process according to further example 6, wherein the plurality of powder particles is characterized by a particle size distribution, and wherein, in the particle size distribution, about 1.5% of the particles by weight are less than about 100 microns, about 15% of the particles by weight are less than about 200 microns, about 35% of the particles by weight are less than 270 microns, and about 55% of the particles by weight are less than about 400 microns. [0072] Further example 38. A process according to further example 1, wherein at least about 75% of the plurality of potassium humate particles are dissolved in five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius. [0073] Further example 39. A process according to further example 1, wherein at least about 90% of the plurality of potassium humate particles are dissolved in five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius. [0074] Further example 40. A process according to further example 1, wherein at least about 95% of the plurality of potassium humate particles are dissolved in five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius. [0075] Further example 41. A process according to further example 1, wherein at least about 99% of the plurality of potassium humate particles are dissolved in five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius. [0076] Further example 42. A process according to further example 1, wherein 100% of the plurality of potassium humate particles are dissolved in five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius. [0077] Further example 43. A process according to further example 1, wherein at least about 75% of the plurality of potassium humate particles are dissolved in one minute when submerged in one liter of water at a temperature of 25 degrees Celsius. [0078] Further example 44. A process according to further example 1, wherein at least about 90% of the plurality of potassium humate particles are dissolved in one minute when submerged in one liter of water at a temperature of 25 degrees Celsius. [0079] Further example 45. A process according to further example 1, wherein at least about 95% of the plurality of potassium humate particles are dissolved in one minute when submerged in one liter of water at a temperature of 25 degrees Celsius. [0080] Further example 46. A process according to further example 1, wherein at least about 99% of the plurality of potassium humate particles are dissolved in one minute when submerged in one liter of water at a temperature of 25 degrees Celsius. [0081] Further example 47. A process according to further example 1, wherein 100% of the plurality of potassium humate particles are dissolved in one minute when submerged in one liter of water at a temperature of 25 degrees Celsius. [0082] Further example 48. A process according to further example 1, wherein obtaining zinc sulfate includes obtaining a commercially available zinc sulfate composition. [0083] Further example 49. A process according to further example 1, wherein obtaining zinc sulfate further includes: obtaining raw materials, including zinc oxide and sulfuric acid; mixing the zinc oxide and the sulfuric acid with water and sodium carbonate, thereby forming a zinc sulfate solution; leaching the zinc sulfate solution, thereby forming a leached zinc sulfate solution; purifying the leached zinc sulfate solution, thereby forming a purified zinc sulfate solution; and filtering the purified zinc sulfate solution through a filter press, retaining all solid precipitates and thereby forming a final zinc sulfate solution. [0084] Further example 50. A process according to further example 49, wherein mixing the zinc oxide and the sulfuric acid with water and sodium carbonate occurs at about 60 degrees Celsius to about 65 degrees Celsius. [0085] Further example 51. A process according to further example 49, wherein the zinc oxide, sulfuric acid, water, and sodium carbonate are mixed for approximately 8 hours. [0086] Further example 52. A process according to further example 49, wherein leaching the zinc sulfate solution additionally includes filtering the zinc sulfate solution, resulting in a brine; subjecting the brine through a water treatment process, resulting in a “cake”, or solidified or semi-solidified sediment. This “cake”, or solidified or semi-solidified sediment, is subjected0 to a counter current washing process, after which the zinc-rich materials are reacted with sulfuric acid, the result of this is passed through a filter press, which retains all non-leachable solids, resulting in a zinc sulfate solution free of particles. [0087] Further example 53. A process according to further example 49, wherein leaching the zinc sulfate solution occurs at a temperature of about 80 degrees Celsius to about 90 degrees Celsius. [0088] Further example 54. A process according to further example 49, wherein purifying the leached zinc sulfate solution includes adding zinc dust to the leached zin sulfate to perform an ion exchange between the zinc, lead and cadmium contents in the solution. [0089] Further example 55. A process according to further example 49, wherein purifying the leached zinc sulfate solution occurs at a temperature of about 70 degrees Celsius to about 80 degrees Celsius. [0090] Further example 56. A process according to further example 49, further includes drying the final zinc sulfate solution for about 15 minutes at about 550 degrees Celsius in order to form zinc sulfate powder. [0091] Further example 57. A process according to further example 1, wherein the potassium humate zinc sulfate compound is a granule, and the process further includes solidifying by an apparatus comprising at least a rotary pelletizing cone and flat surface (e.g. conveyor belt). [0092] Further example 58. A process according to further example 57, wherein the granulating occurs at a temperature ranging between about 65 degrees Fahrenheit and about 190 degrees Fahrenheit. This low temperate is important to preserve the benefits of the potassium humate powder. Granulating at too high of a temperature for a lengthy period of time may result in denaturing the active components of the potassium humate. [0093] Further example 59. A process according to further example 57, wherein the flat surface is a steel belt. [0094] Further example 60. A process according to further example 59, wherein the solidifying further includes cooling the mixture on the flat surface. [0095] Further example 61. A process according to further example 60, wherein the cooling is effectuated by spraying a cooled liquid solution (e.g., 40 to 50 degrees Fahrenheit), for example water, on the underside of the steel belt, resulting in the cooling of the belt and subsequently the homogenized mixture deposited thereon. [0096] Further example 62. A process according to further example 60, wherein the cooling is effectuated by moving the belt into, or through, a chiller. In some instances, such a chiller may be set to about 40 to 50 degrees Fahrenheit, although this is not to be understood as limiting. [0097] Further example 63. A process according to further example 60, wherein the cooling may be any other active means of cooling known in the art, such as other forms of refrigeration or freezing. [0098] Further example 64. A process according to further example 60, wherein the cooling may be a passive means of cooling; for example the cooling may be simply allowing the mixture to cool to room temperature without any further intervention. [0099] Further example 65. A process according to further example 57, wherein the process further includes passing the resulting granules through a sized screen to produce a desired granule size. [0100] Further example 66. A process according to further example 57, wherein the potassium humate zinc sulfate compound granule is between about 0.5 mm and about 5.0 mm. [0101] Further example 67. A process according to further example 57, wherein the potassium humate zinc sulfate compound granule is between about 0.8 mm and about 4.0 mm. [0102] Further example 68. A process according to further example 57, wherein the potassium humate zinc sulfate compound granule is between about 0.8 mm and about 1.99 mm. [0103] Further example 69. A process according to further example 1, wherein the potassium humate zinc sulfate compound granule is between about 2.0 mm and about 4.0 mm. [0104] Further example 70. A process according to further example 1, wherein the potassium humate zinc sulfate compound granule has a pH of at least 2. [0105] Further example 71. A process according to further example 1, wherein the potassium humate zinc sulfate compound granule has a pH of 2 to about 12. [0106] Further example 72. A process according to further example 1, wherein the potassium humate zinc sulfate compound granule has a pH of about 7. [0107] Further example 73. A process according to further example 1, wherein the process further includes applying the potassium humate zinc sulfate compound to a desired site, such as an agriculture setting. [0108] Aspects of a potassium humate zinc sulfate compound such as is described in various embodiments herein are further illustrated by the following further examples, which are set forth to illustrate certain aspects of the potassium humate zinc sulfate compound described in various embodiments herein and are not to be construed as limiting thereof. [0109] Further example 74. A potassium humate zinc sulfate compound, the compound made by a process comprising: obtaining a plurality of fully-soluble potassium humate powder particles; obtaining a zinc sulfate compound; and mixing the plurality of potassium humate particles with the zinc sulfate, thereby forming a homogenized mixture; thereby forming a potassium humate zinc sulfate compound configured to be applied to a soil surface. [0110] Further example 75. A potassium humate zinc sulfate compound comprising: a powder potassium humate component, wherein at least 95% of the plurality of potassium humate powder particles dissolve within five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius; a zinc sulfate component; wherein the powder potassium humate component and the zinc sulfate are homogenized at a ratio ranging between about 1:399 to and about 1:3; wherein the potassium humate zinc sulfate compound has a pH of 2 to about 12. [0111] Further example 76. A potassium humate zinc sulfate compound according to further example 75, wherein the potassium humate zinc sulfate compound is a powder. [0112] Further example 77. A potassium humate zinc sulfate compound according to further example 75, wherein potassium humate zinc sulfate compound is a granule. [0113] Further example 78. A potassium humate zinc sulfate compound according to further example 77, wherein the potassium humate zinc sulfate compound granule is between about 0.5 mm and about 5.0 mm. [0114] Further example 79. A potassium humate zinc sulfate compound according to further example 77, wherein the potassium humate zinc sulfate compound granule is between about 0.8 mm and about 4.0 mm. [0115] Further example 80. A potassium humate zinc sulfate compound according to further example 77, wherein the potassium humate zinc sulfate compound granule is between about 0.8 mm and about 1.99 mm. [0116] Further example 81. A potassium humate zinc sulfate compound according to further example 77, wherein the potassium humate zinc sulfate compound granule is between about 2.0 mm and about 4.0 mm. [0117] Further example 82. A potassium humate zinc sulfate compound according to further example 75, wherein the potassium humate zinc sulfate compound is configured to be applied to a desired location. [0118] Further example 83. A potassium humate zinc sulfate compound according to further example 82, wherein the desired location is an agricultural soil. [0119] Further example 84. A potassium humate zinc sulfate compound according to further example 82, wherein the potassium humate zinc sulfate compound granules between about 2.0 mm and about 4.0 mm may be applied to agricultural soils. [0120] Further example 85. A potassium humate zinc sulfate compound according to further example 82, wherein the potassium humate zinc sulfate compound granules between about 0.8 mm and about 1.99 mm may be applied to turf soils. [0121] Further example 86. A plurality of potassium humate zinc sulfate granules according to further example 77, are illustrated in Figures 2A-B. As evident by Figures 2A-B the granules may generally vary in shape and size, and in some instances varying sizes and shapes may be utilized for different purposes. For example, in some instances smaller composite granules (e.g. about 0.8 to about 1.99 mm in diameter), such as those illustrated in Figures 2A, may be utilized in turf applications (e.g. on golf courses, lawn maintenance, etc.). In other instances, larger granules (e.g. about 2.0 to about 4.0 mm in diameter), such as those illustrated in Figure 2B, may be utilized in agricultural applications. However, it is to be understood that these examples are for illustrative purposes only and are non-limiting. [0122] Further example 87. A plurality of potassium humate zinc sulfate granules according to further example 86 were subjected to crush strength testing. The composite granules were separated by size, with potassium humate zinc sulfate granules ranging from about 0.8 to 1.99 mm in diameter being tested together and potassium humate zinc sulfate granules ranging from about 2.0 to about 4 mm in diameter being tested together. Crush strength testing was conducted for granules ranging from about 0.8 to 1.99 mm in diameter and for granules ranging from about 2.0 to about 4.0 mm in diameter, respectively. SGN, or Size Guide Number is a standard measurement of the diameter, as expressed in millimeters x 100, of granules based on the median within the batch. As illustrated in Table 1, the crush strength measurements of the granules ranging from about 0.8 to 1.99 mm in diameter range from about 6.5 psi to about 8.0 psi. The crush strength measurements of the granules ranging from about 2.0 to 4.0 mm in diameter range from about 3.5 psi to about 5.0 psi. However, it is to be understood that these examples are for illustrative purposes only and are non-limiting, in some instances the crush strength of a granule consistent with the description herein may range anywhere from 0.1 psi to 10 psi. Table 1.
Figure imgf000021_0001
[0123] Many modifications and other embodiments of a process such as is described in various embodiments herein will come to mind to one skilled in the art to which this disclosed process pertains having the benefit of the teachings presented in the foregoing description. Therefore, it is to be understood that a process such as is described in various embodiments herein is not to be limited to the specific embodiments disclosed and that modifications and other embodiments are intended to be included within the scope of the appended claims. Although specific terms are employed herein, they are used in a generic and descriptive sense only and not for purposes of limitation.

Claims

WHAT IS CLAIMED: 1. A process for making a potassium humate zinc sulfate compound, the process comprising: obtaining a plurality of fully-soluble potassium humate powder particles; obtaining a zinc sulfate compound; and mixing the plurality of potassium humate particles with the zinc sulfate compound, thereby forming a homogenized mixture; thereby forming a potassium humate zinc sulfate compound configured to be applied to a soil surface. 2. The process for making a potassium humate zinc sulfate compound of claim 1, wherein the potassium humate zinc sulfate compound is a powder. 3. The process for making a potassium humate zinc sulfate compound of claim 1, wherein the process further includes: adding a binder to the homogenized mixture; and granulating the homogenized mixture into a granule, thereby making a potassium humate zinc sulfate compound granule. 4. The process for making a potassium humate zinc sulfate compound of claim 3, wherein the binder is water. 5. The process for making a potassium humate zinc sulfate compound of claim 3, wherein the granulating occurs at a temperature ranging between about 65 degrees Fahrenheit and about 190 degrees Fahrenheit. 6. The process for making a potassium humate zinc sulfate compound of claim 1, wherein obtaining the plurality of fully-soluble potassium humate powder particles further includes: obtaining a sample of a carbonaceous substance comprising humic acid and one or more other substances; contacting the sample with an amount of an alkaline mixture, thereby forming an extraction mixture, the extraction mixture consisting essentially of a sludge component; the sludge component comprising, predominantly, the sample, and an extraction component, the extraction component comprising, predominantly, the alkaline mixture; maintaining the sludge component in contact with the extraction component for a period of time sufficient for the extraction component to become relatively enriched in humic acid and the sludge component to become relatively depleted of humic acid; separating the sludge component from the extraction component; and spray drying the extraction component, thereby forming the plurality of potassium humate powder particles. 7. The process for making a potassium humate zinc sulfate compound of claim 1, wherein the zinc sulfate compound is a powder zinc sulfate. 8. The process for making a potassium humate zinc sulfate compound of claim 1, wherein the homogenized mixture includes about 5 pounds to about 500 pounds of the plurality of potassium humate powder particles to about 1,995 pounds to about 1,500 pounds of zinc sulfate. 9. The process for making a potassium humate zinc sulfate compound of claim 1, wherein the potassium humate zinc sulfate compound has a pH of 7.5 to about 12. 10. The process for making a potassium humate zinc sulfate compound of claim 1, wherein at least 95% of the plurality of potassium humate powder particles dissolve within five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius. 11. A process for making a potassium humate zinc sulfate compound, the process comprising: obtaining a plurality of potassium humate powder particles; wherein at least 95% of the plurality of potassium humate powder particles dissolve within five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius; obtaining a zinc sulfate compound; and mixing the plurality of potassium humate particles with the zinc sulfate, thereby forming a homogenized mixture; wherein the homogenized mixture includes about 5 pounds to about 500 pounds of the plurality of potassium humate powder particles to about 1,995 pounds to about 1,500 pounds of zinc sulfate compound; thereby forming a potassium humate zinc sulfate compound configured to be applied to a soil surface. 12. The process for making a potassium humate zinc sulfate compound of claim 11, wherein the potassium humate zinc sulfate compound is a powder. 13. The process for making a potassium humate zinc sulfate compound of claim 11, wherein the process further includes: adding a binder to the homogenized mixture; granulating the homogenized mixture into a granule, thereby making a potassium humate zinc sulfate compound granule. 14. The process for making a potassium humate zinc sulfate compound of claim 13, wherein the binder is water. 15. The process for making a potassium humate zinc sulfate compound of claim 13, wherein the granulating occurs at a temperature ranging between about 65 degrees Fahrenheit and about 190 degrees Fahrenheit. 16. The process for making a potassium humate zinc sulfate compound of claim 11, wherein the potassium humate zinc sulfate compound has a pH of 2 to about 12. 17. A potassium humate zinc sulfate compound, the compound comprising: a powder potassium humate component, wherein at least 95% of the plurality of potassium humate powder particles dissolve within five minutes when submerged in one liter of water at a temperature of 25 degrees Celsius; a zinc sulfate component; wherein the powder potassium humate component and the zinc sulfate component are homogenized at a ratio ranging between about 1:399 to and about 1:3; wherein the potassium humate zinc sulfate compound has a pH of 2 to about 12. 18. The potassium humate zinc sulfate compound of claim 17, wherein the compound is a powder configured to be applied to a soil surface. 19. The potassium humate zinc sulfate compound of claim 17, wherein the potassium humate zinc sulfate compound is a granule.
PCT/US2021/041100 2020-07-09 2021-07-09 Potassium humate zinc sulfate compound WO2022011268A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CA3185134A CA3185134A1 (en) 2020-07-09 2021-07-09 Potassium humate zinc sulfate compound
MX2023000422A MX2023000422A (en) 2020-07-09 2021-07-09 Potassium humate zinc sulfate compound.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US16/924,856 2020-07-09
US16/924,856 US11691999B2 (en) 2014-06-18 2020-07-09 Homogenous humate powder compositions exhibiting high solubility

Publications (1)

Publication Number Publication Date
WO2022011268A1 true WO2022011268A1 (en) 2022-01-13

Family

ID=79552122

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2021/041100 WO2022011268A1 (en) 2020-07-09 2021-07-09 Potassium humate zinc sulfate compound

Country Status (3)

Country Link
CA (1) CA3185134A1 (en)
MX (1) MX2023000422A (en)
WO (1) WO2022011268A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11597688B1 (en) 2014-06-18 2023-03-07 Humic Growth Solutions, Llc Process for making a fully water-soluble granule comprising humic acid and a microbial community composition
US11691999B2 (en) 2014-06-18 2023-07-04 Humic Growth Solutions. Llc Homogenous humate powder compositions exhibiting high solubility

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102718605A (en) * 2012-07-19 2012-10-10 湖南省烟草公司郴州市公司 Method for producing amino acid tobacco-specific foliar fertilizer by using abandoned fur
CN107746331A (en) * 2017-11-10 2018-03-02 安徽辉隆集团五禾生态肥业有限公司 A kind of trace element water-soluble fertilizer for strengthening wettability and preparation method thereof
CN109485501A (en) * 2018-12-05 2019-03-19 李秀芹 Increase production disease-resistant water-soluble fertilizer and preparation method thereof for the swollen fruit colouring of fruits and vegetables
CN110734334A (en) * 2019-11-27 2020-01-31 衡阳县蒸湛农业发展有限公司 Tillering fertilizer special for kinds of rice

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102718605A (en) * 2012-07-19 2012-10-10 湖南省烟草公司郴州市公司 Method for producing amino acid tobacco-specific foliar fertilizer by using abandoned fur
CN107746331A (en) * 2017-11-10 2018-03-02 安徽辉隆集团五禾生态肥业有限公司 A kind of trace element water-soluble fertilizer for strengthening wettability and preparation method thereof
CN109485501A (en) * 2018-12-05 2019-03-19 李秀芹 Increase production disease-resistant water-soluble fertilizer and preparation method thereof for the swollen fruit colouring of fruits and vegetables
CN110734334A (en) * 2019-11-27 2020-01-31 衡阳县蒸湛农业发展有限公司 Tillering fertilizer special for kinds of rice

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
ANONYMOUS: "Potassium humate - Wikipedia", 3 May 2019 (2019-05-03), pages 1 - 1, XP055846132, Retrieved from the Internet <URL:https://en.wikipedia.org/wiki/Potassium_humate> [retrieved on 20210930] *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11597688B1 (en) 2014-06-18 2023-03-07 Humic Growth Solutions, Llc Process for making a fully water-soluble granule comprising humic acid and a microbial community composition
US11691999B2 (en) 2014-06-18 2023-07-04 Humic Growth Solutions. Llc Homogenous humate powder compositions exhibiting high solubility

Also Published As

Publication number Publication date
CA3185134A1 (en) 2022-01-13
MX2023000422A (en) 2023-05-12

Similar Documents

Publication Publication Date Title
US11136505B2 (en) Potassium Humate sulfur compound granule
US9919977B2 (en) Synthetic gypsum fertilizer product and method of making
CA2570565C (en) Method for extracting fulvic acid molecules
WO2022011268A1 (en) Potassium humate zinc sulfate compound
EP3638641A1 (en) Compacted polyhalite and potash mixture and a process for the production thereof
US10723667B1 (en) Fully water-soluble granule enriched in humic acid
US11136275B2 (en) Process for making a composite granule with rock phosphate, sulfur, and humic acid
US20220162133A1 (en) Polyhalite and potash granules
JP2020537623A (en) The process of producing humus from biomass such as wood, bark, grain straw, leaves, herbaceous plants, wood fungi, sewage sludge and other organic wastes.
US20230357299A1 (en) Potassium Humate Zinc Sulfate Compound
US9914670B1 (en) Process for making a fully water-soluble humic acid granule
EA018664B1 (en) Sulphur-containing fertilizers and process for the preparation thereof
EP3666746A1 (en) Pedosphere enhancing granules, method of making and using same
BR112021009934A2 (en) compacted polyhalite and a process for producing it
WO2021033178A1 (en) Granules of polyhalite, potash and ammonium sulphate and a compaction process for the production thereof
CA3077954A1 (en) Process for making a composite granule with rock phosphate, sulfur, and humic acid
US11390570B1 (en) Humic acid-supplemented fertilizers, macronutrients, and micronutrients
CA3070820A1 (en) Potassium humate sulfur compound granule
CN114804955A (en) Soluble slow-release type soil improvement and conditioning multielement fertilizer and preparation process thereof
EP2167428A2 (en) Method of preparation of granulated industrial nitrogen-calcium fertilizer
RU2184103C1 (en) Method to obtain complex organomineral fertilizer
SU1479446A1 (en) Method of producing non-dusting potassium fertilizer
CZ2022378A3 (en) The method of producing a fertilizer from energy gypsum, a fertilizer and its use
WO2023067591A1 (en) A granule of kieserite and a process for the production thereof
EA043194B1 (en) POWDER-LIKE WATER-SOLUBLE HUMINO-CONTAINING PRODUCT FROM PEAT, METHOD FOR ITS PRODUCTION AND FERTILIZER ON ITS BASIS

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 21746903

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 3185134

Country of ref document: CA

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 21746903

Country of ref document: EP

Kind code of ref document: A1