WO2010058038A1 - Procédé de fabrication d’un engrais contenant du soufre élémentaire - Google Patents

Procédé de fabrication d’un engrais contenant du soufre élémentaire Download PDF

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Publication number
WO2010058038A1
WO2010058038A1 PCT/EP2010/052042 EP2010052042W WO2010058038A1 WO 2010058038 A1 WO2010058038 A1 WO 2010058038A1 EP 2010052042 W EP2010052042 W EP 2010052042W WO 2010058038 A1 WO2010058038 A1 WO 2010058038A1
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WO
WIPO (PCT)
Prior art keywords
sulphur
elemental sulphur
dispersion
fertilizer
elemental
Prior art date
Application number
PCT/EP2010/052042
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English (en)
Inventor
Rafael Alberto Garcia Martinez
Klaas J Hutter
Original Assignee
Shell Internationale Research Maatschappij B.V.
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
Application filed by Shell Internationale Research Maatschappij B.V. filed Critical Shell Internationale Research Maatschappij B.V.
Priority to US13/319,230 priority Critical patent/US8679219B2/en
Priority to EP10704154.3A priority patent/EP2429975B1/fr
Priority to MA34425A priority patent/MA33344B1/fr
Priority to NZ596251A priority patent/NZ596251A/en
Priority to MX2011011823A priority patent/MX2011011823A/es
Priority to BRPI1011638-9A priority patent/BRPI1011638B1/pt
Priority to CN2010800265110A priority patent/CN102459130A/zh
Priority to AU2010202235A priority patent/AU2010202235B2/en
Publication of WO2010058038A1 publication Critical patent/WO2010058038A1/fr
Priority to IL216111A priority patent/IL216111A0/en
Priority to TNP2011000556A priority patent/TN2011000556A1/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C05—FERTILISERS; MANUFACTURE THEREOF
    • C05D—INORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C; FERTILISERS PRODUCING CARBON DIOXIDE
    • C05D9/00—Other inorganic fertilisers
    • C—CHEMISTRY; METALLURGY
    • C05—FERTILISERS; MANUFACTURE THEREOF
    • C05B—PHOSPHATIC FERTILISERS
    • C05B1/00—Superphosphates, i.e. fertilisers produced by reacting rock or bone phosphates with sulfuric or phosphoric acid in such amounts and concentrations as to yield solid products directly
    • C—CHEMISTRY; METALLURGY
    • C05—FERTILISERS; MANUFACTURE THEREOF
    • C05G—MIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
    • C05G5/00—Fertilisers characterised by their form
    • C05G5/10—Solid or semi-solid fertilisers, e.g. powders
    • C05G5/12—Granules or flakes

Definitions

  • the present invention provides a process for the preparation of an elemental sulphur-containing fertilizer.
  • Canola is an important cash crop in Alberta, Canada, and has high sulphur requirements at any growth stage. A shortage of sulphur can cause serious reductions in crop yield and quality.
  • Manufacturing processes for sulphur-containing fertilizers of the phosphate type often involve the use or incorporation of sulphates.
  • a disadvantage of sulphates is that they are very mobile in the soil and easily leach out of the root zone, effectively making the sulphate nutrient unavailable to the plants. Elemental sulphur is not leached out of the soil as readily as sulphates. Instead, micron-sized elemental sulphur particles (e.g. with size from 1 to 200 ⁇ m) are oxidized to sulphate sulphur, which is the form utilised by the plants, by soil bacteria during the cropping season.
  • Elemental sulphur can therefore be considered a slow (timed) release form of plant nutrient sulphur that is less prone to leaching out of the crops root zone. It is, therefore, advantageous to have a large proportion of the sulphur in fertilizers present as elemental sulphur.
  • elemental sulphur offers some additional benefits in agriculture, including acting as a fungicide against certain micro organisms, acting as a pesticide against certain soil and plant pests, assisting the decomposition of plant residues and improving phosphorus and nitrogen nutrient utilisation and reducing the pH of alkaline and calcareous soils.
  • NZ 213682 discloses a method for providing sulphur for use in a sulphur-containing fertilizer wherein liquid sulphur is added to phosphoric acid, wherein the phosphoric acid is in a high energy state of shear in a high energy vortex. This provides a dispersion of sulphur in phosphoric acid, which can be used in the formation of sulphur-containing triple superphosphate fertilizer.
  • US 4,372,872 discloses a process wherein a suspension of sulphur is produced by agitating an aqueous medium with a high shear mixer, and introducing sulphur (in particulate or molten form ⁇ into the agitated medium.
  • the sulphur suspensions can be applied to the soil.
  • the present inventors have found that, with such methods of preparing sulphur for incorporation into fertilizer products, it is difficult to avoid providing relatively large sulphur particles and these larger particles lead to operational difficulties during fertilizer manufacture such as build-up of particles in the apparatus and possible plugging of the process equipment and process lines. Also, said relatively large sulphur particles are more difficult to incorporate into and bond to the other fertilizer material.
  • WO 2008/089568 discloses a method for wet grinding sulphur feedstock wherein hydrocyclones are used to separate elemental sulphur particles having selected size distributions. The product can be further processed to produce a sulphur-based fertilizer.
  • a ball mill is used as a primary grinding stage and a Vertimill as a second grinding unit.
  • a disadvantage of this wet grinding process is its process complexity (a number of pieces of process equipment is needed) and that the process is energy intensive. No mention of a dispersion mill is made.
  • step (a) mixing ammonia, phosphoric acid and water in a reactor unit to obtain an ammonium phosphate mixture; (b) introducing the mixture obtained in step (a) into a granulator unit to obtain granules, wherein a liquid phase comprising elemental sulphur is brought into contact with ammonia, phosphoric acid and water in the reaction unit in step (a) or is introduced in the granulator in step (b) . No mention is made of milling the elemental sulphur.
  • US 5 522 553 discloses a dispersion mill and more particularly a method and apparatus for producing liquid - A -
  • the present inventors have sought to provide an alternative method for manufacturing elemental sulphur- containing fertilizer.
  • the present inventors have sought to provide a simpler and less energy intensive process for manufacturing elemental sulphur-containing fertilizer.
  • the present inventors have sought to provide a process for manufacturing elemental sulphur- containing fertilizer, wherein the particle size of the elemental sulphur particles can be easily controlled.
  • the present invention provides a process for preparing an elemental sulphur-containing fertilizer, comprising steps of:
  • An important advantage of the process according to the present invention is that it enables to select and closely control (or manage) the size and size distribution of the sulphur particles in the fertilizer product, which is advantageous as the efficacy of the sulphur-enhanced fertilizer is affected by the sulphur particle size and particle size distribution.
  • the actual size and size distribution of the sulphur particles in the fertilizer product can be selected for example dependent on the agricultural environments (e.g. soil and climatic conditions) for which the fertilizer is intended.
  • step (a) of the process of the invention elemental sulphur in a liquid (preferably an aqueous liquid) is wet milled in a dispersion mill, wherein a rotor turns within a slotted stator, thereby providing a dispersion of milled elemental sulphur in the liquid.
  • the liquid and elemental sulphur are drawn by the rotation of the rotor into the rotor/stator assembly, and are accelerated and expelled radially through the openings in the slotted stator. With each pass through the rotor/stator assembly, the elemental sulphur is subjected to a combination of mechanical and hydraulic shear such that the particles of elemental sulphur are reduced in size.
  • the rotor turns at very high speeds, preferably such that the tip speed is from 1500 to 3500 metres per minute, more preferably from 2000 to 3000 metres per minute. Higher tip speeds result in a higher energy input in the dispersion mill and result in a smaller average sulphur particle size. The speed should be sufficiently high to achieve the required particle size.
  • a preferred dispersion mill has a slotted rotor inside a slotted stator. When the rotor and stator slots come into alignment, the liquid and elemental sulphur are ejected from the rotor slots into the stator slots.
  • Suitable dispersion mills are described in US 5 522 553 and are available from Kady International, USA.
  • the elemental sulphur used in the fertilizer composition and process of the present invention can be obtained from any suitable source. In one embodiment of the present invention, the elemental sulphur is obtained from an industrial process, such as the removal of unwanted sulphur components from natural gas.
  • the elemental sulphur used may be high purity (> 99.9% S) chemical sulphur as obtained from the Claus process.
  • the process of the present invention can use elemental sulphur of significantly lower purity than this.
  • elemental sulphur containing materials are sulphur filter cake as obtained from sulphur melting and filtration operations and sulphur obtained from a various chemical and biological H 2 S gas removal processes.
  • sulphur sources may contain anywhere in the range of from 30 to 99.9 wt.%, preferably from 50 to 99.5 wt.%, more preferably from 60 to 99.0 wt.%, sulphur.
  • Sulphur may be added to the dispersion mill as molten sulphur or as solid sulphur, but is preferably added as solid sulphur because this avoids having to keep the sulphur at a high temperature (sulphur is molten above 120 0 C) .
  • the sulphur is preferably added as pellets, e.g. rotoformed pellets of average size from 3 to 4 mm.
  • the liquid in step (a) may be chosen from a broad variety of liquids but is preferably an aqueous liquid.
  • the aqueous liquid may be an acidic aqueous solution such as an aqueous solution of phosphoric acid or sulphuric acid, and is most preferably selected from an aqueous solution of phosphoric acid, an aqueous solution of ammonium phosphate, an aqueous solution of ammonium sulphate and a combination thereof.
  • the phosphoric acid preferably has a strength corresponding to from 1 to 60% of P 2 O 5 in water, more preferably from 5 to 50%.
  • the aqueous liquid contains as little water as possible to avoid the introduction of excess process water; any excess water that is introduced into the fertilizer production process is to be eliminated at a later stage and thereby leads to a more complex and more energy intensive process.
  • the weight percentage of elemental sulphur based upon the combined weight of the sulphur and the aqueous liquid in step (a) is preferably from 10 to 70 wt.%, more preferably from 5 to 50 wt.%, even more preferably from 10 to 40 wt.%.
  • one or more surfactants are added during step (a) or step (b) .
  • the surfactant (s) may be added to the liquid before the elemental sulphur is wet milled, or may be added to the dispersion of milled elemental sulphur before or during the combination with further components.
  • the surfactants may help to further reduce the production of sulphur dust during fertilizer manufacture, may aid the granulation of the fertilizer in step (c) and may reduce the viscosity of the elemental sulphur dispersion produced in step (a) and/or elemental sulphur mixture produced in step (b) .
  • the surfactants could include cationic surfactants such as the ethylene oxide or propylene oxide adduct of an aliphatic amine, or could include anionic surfactants such as a lignosulphonate.
  • the one or more surfactants are added in such an amount that the granulated elemental sulphur-containing fertilizer as produced in step (c) comprises from 0.001 to 5.0 wt . % surfactant, preferably from 0.10 wt.% to 1.5 wt.%, based on the total weight of the granulated fertilizer.
  • step (a) the liquid is added to the dispersion mill first, the mill is started and then the sulphur is added over a relatively short period of time.
  • the addition rate for the sulphur is preferably as fast as possible without overloading the mill.
  • the energy input during the milling can be expressed as power per volume or mass of sulphur processed, e.g. kWh/m 3 sulphur processed or kWh/ton sulphur processed.
  • the energy input affects the size of the milled sulphur particles in the resulting dispersion, so is chosen according to the required particle size. Higher energy input provides smaller particle sizes. For a particular mill, higher energy input can be achieved by reducing the amount of sulphur that is milled.
  • the energy input is from 10 (preferably above 20) to 1000 kWh/ton sulphur processed, more preferably from 50 to 100 kWh/ton sulphur processed, even more preferably from 65 to 85 kWh/ton sulphur processed.
  • step (a) Part of this higher energy will be transferred to the dispersion being formed in step (a) as thermal energy thereby increasing the temperature thereof.
  • Such temperature increase can be controlled using a suitable heat exchanger (possibly incorporated in the dispersion mill) .
  • Preferred temperatures for wet milling of elemental sulphur are between 0 and 120 0 C, more preferably between 15 and 80 0 C. In some embodiments, this temperature increase avoids any additional heating steps thereby saving energy and equipment costs.
  • An advantage of the process of the invention is that by controlling the parameters in step (a) , specifically the size of slots in the stator and optionally the rotor, the tip speed of the rotor and the energy input, and/or the physical-chemical properties of the liquid ⁇ composition, temperature, viscosity) , it is possible to control the particle size and particle size distribution of the resulting dispersion. It is important to be able to control the sulphur particle size because the particle size affects the effectiveness (rate of release) of the sulphur fertilizer. The rate of oxidation of the sulphur particles to sulphate is affected by the particle size, see e.g. Boswell et al, Fertilizer Research 35, 127-149, 1993.
  • the present invention enables the skilled person to produce elemental sulphur-containing fertilizer with sulphur particle size tailored for a specific agricultural environment .
  • the present invention provides sulphur particles with a shape that has a higher surface area to volume ratio than the substantially spherical particles produced in other processes such as (wet) prilling processes.
  • Particles with a high surface area to volume ratio are preferred because oxidation of sulphur will be faster with a higher surface area (see Watkinson et al, Fertilizer Research 35, 115-126, 1993) .
  • sulphur particles with a high surface area to volume ratio may also have better wettability such that they are more readily incorporated into sulphur fertilizer with better adhesion and less generation of sulphur dust during the granulation step
  • the elemental sulphur-containing fertilizer is a sulphur - triple super phosphate fertilizer
  • the liquid is an aqueous solution of phosphoric acid
  • step (b) the dispersion of milled elemental sulphur in phosphoric acid solution is mixed and reacted with phosphate rock, thereby providing a mixture of sulphur and soluble calcium phosphate.
  • the phosphoric acid preferably has a strength of from 5 to 60 wt.% P 2 O 5 , more preferably from 10 to 50 wt.% P 2 O 5 and the resulting dispersion of milled sulphur in phosphoric acid preferably comprises from 1 to 60 wt.% sulphur and from 5 to 55 wt.% P 2 O 5 based upon the weight of the dispersion, more preferably from 20 to 40 wt.% sulphur and from 10 to _ i i _
  • step (b) the relative amounts of the phosphate rock and the dispersion of elemental sulphur in phosphoric acid are preferably set such that the R ratio (the ratio of P 2 Os from the phosphate rock to P 2 O 5 from phosphoric acid) is from 2.0 to 2.8 (this will vary with the quality of the phosphate rock and phosphoric acid) .
  • step (b) the dispersion of milled elemental sulphur is combined with phosphate rock using methods known to the skilled person.
  • non-granular triple super phosphate which is used as an intermediate for production of compound fertilizer by granulation processes
  • the dispersion of milled elemental sulphur can be combined with phosphate rock in a suitable mixer such as a cone mixer.
  • finely ground phosphate rock ⁇ e.g. 80% passing 200 mesh
  • the dispersion of milled elemental sulphur at 90 to 105 0 C ⁇ possibly with the addition of steam to attain these temperatures
  • the elemental sulphur-containing fertilizer is a sulphur - monoammonium phosphate, sulphur diammonium phosphate or sulphur - nitrogen/phosphorus/potassium fertilizer
  • step (b) the dispersion of milled elemental sulphur in liquid is mixed and reacted with ammonia, thereby providing a mixture of sulphur and ammonium phosphate.
  • step ⁇ a) preferably an aqueous solution of phosphoric acid is used as the liquid and preferably has a strength of from 5 to 60 wt.% P 2 O 5 , more preferably from 10 to 50 wt.
  • % P 2 O 5 and the resulting dispersion of milled sulphur in phosphoric acid preferably comprises from 1 to 60 wt.% sulphur and from 5 to 55 wt.% P 2 O 5 based upon the weight of the dispersion, more preferably from 20 to 50 wt.% (preferably below 40 wt.%) sulphur and from 10 to 50 wt.% P 2 O 5 .
  • the amount of ammonia is determined by the required product.
  • the molar ratio of ammonia and phosphoric acid is typically kept between values of from 0.5 to 1.0.
  • the molar ratio of ammonia and phosphoric acid is typically kept between values of from 1.2 to 2.0.
  • sulphur - nitrogen/phosphorus/potassium fertilizer the molar ratio of ammonia and phosphoric acid is typically kept between values of from 0.7 to 1.7.
  • the dispersion of elemental sulphur and the ammonia are preferably mixed in step (b) in a pre-neutraliser or a pipe cross reactor.
  • the ammonia is preferably supplied as anhydrous ammonia.
  • the reaction of the phosphoric acid and the ammonia is exothermic and typically results in vigorous mixing in a pre-neutraliser or pipe cross reactor such that no further agitation is required.
  • Residence time in a pipe cross reactor is preferably just a few seconds, e.g. 1-5 seconds. Residence time in a pre- neutraliser is likely to be longer, e.g. from 30 to 60 minutes.
  • sulphur - nitrogen/phosphorus/potassium fertilizer it is necessary to incorporate potassium into the fertilizer. This can be achieved in step (b) by mixing the dispersion of milled elemental sulphur in phosphoric acid with ammonia and with a potassium salt. Alternatively, this can be achieved in step (c) by adding a potassium salt to the granulator unit. Also, this can be achieved in step (a) or before by adding a potassium salt (or solution thereof) before or during the wet milling.
  • step (c) of the process of the invention the mixture of elemental sulphur and further components is granulated in a granulator unit to provide granulated elemental sulphur fertilizer.
  • granulator unit is used to describe a device for forming granules of fertilizer product. Commonly used granulators are described in Perry' s Chemical Engineers' Handbook, chapter 20 (1997) . Preferred granulators are drum granulators, paddle mixers (pug mills) or pan granulators. Preferably, the mixture is pumped and distributed on a rolling bed of material in a drum granulator. Optionally, water and steam can be fed to the granulator to control the temperature of the granulation process as needed.
  • recycled fertilizer particles may be added to the granulator unit.
  • Recycled fertilizer particles add granulation and nucleating agents. They are obtained from the final fertilizer product. Suitably they have small particle sizes (so- called off-spec fines) .
  • Other ingredients may be added during the manufacturing process to tailor the fertilizer products to their intended end-use. Examples include plant micro- nutrients such as boron, potassium, sodium, zinc, manganese, iron, copper, molybdenum, cobalt, calcium, magnesium and combinations thereof. These nutrients may be supplied in elemental form or in the form of salts, for examples as sulphates, nitrates or halides.
  • the amount of plant micronutrients depends on the type of fertilizer needed and is typically in the range of between 0.1 to 5%, based on the total weight of the granules.
  • the granulated elemental sulphur fertilizer obtained in step (c) is preferably dried in a drying unit.
  • the fertilizer is air-dried in the drying unit, thereby avoiding the need for additional drying equipment.
  • drying units wherein heat transfer for drying is accomplished by direct contact between the wet solid and hot gases are used, thereby enabling a faster drying step.
  • the drying unit is a rotary dryer.
  • the granulated elemental sulphur fertilizer granules are sorted on their size in a sorting unit to achieve a more uniform size distribution.
  • a preferred size range for the fertilizer granules is from 1.5 to 5.0 mm, more preferably from 2 to 4 mm, expressed as the average diameter of the granules. The use of granules which fall within this range is more likely to enable a more even distribution of the fertilizer ingredients in the soil after applying the granules to the soil.
  • the particle size and particle size distribution of the milled elemental sulphur in the dispersion provided in step (a) is controlled.
  • the particle size and particle size distribution are controlled by controlling one or more of: the size of slots in the stator, the size of slots in the rotor, the tip speed of the rotor, the energy input, and the physical-chemical properties (composition, temperature, viscosity) of the liquid.
  • a dispersion mill manufactured by Kady International (model OC-30, stainless steel, cooling jacketed, 20-60 gallons of working capacity, equipped with a 30 HP Drive and a variable frequency controller) was used to mill elemental sulphur.
  • the dispersion mill was filled with 200-300 kg of 40-50% P 2 O 5 commercial fertilizer grade phosphoric acid.
  • the unit was started at minimum speed, and the required amount of solid sulphur pastilles (formed yellow bright chemical sulphur) was fed to the unit at a constant and fast pace, to make the targeted slurry concentration (10 to 60 wt.%, depending on the experiment) .
  • the speed was increased to the planned value, and the chronometer was started to keep track of batch residence times. Data was registered during the residence time (e.g. current consumption, time, temperature, visual observations, etc) . Also samples could be taken during the milling.
  • a temperature limit had been set for a particular experiment, cooling water to jacket was started at that temperature (usually 50-80 0 C; in the shown examples, when temperatures were not indicated, the temperature was set at 55-6O 0 C) .
  • a viscosity modifier was used (calcium lignosulphonate, an anionic surfactant available from Borregaard-Lignotech (Rothschild, WI, USA), in a proportion between 0.025 wt.% and 5.0 wt.% based on the weight of the slurry being formed.
  • Energy consumption in kWh/ton sulphur processed was 70.9 (30/52/18), 68.2 (40/56/20), 63.8 (50/53/25) and 52.2 (60/48/28).
  • Molten elemental sulphur was prepared in two flat- bottomed, steam-jacketed tanks (melters) having a working volume of 30 to 40 1; the melters were equipped with variable-speed agitators with two downward-thrust impellers on the shaft.
  • the required amount of elemental sulphur (ES) pastilles was fed to the melters manually.
  • the same dispersion mill as used above Karl OC-30 was filled with a predetermined amount (see again Table IB) of phosphoric acid and/or water, which directly correlated to the amount of molten ES needed to achieve the desired ES percentage in the batch.
  • the rotor of the dispersion mill was turned on and once the speed of the rotor had reached approximately half of the maximum, the addition of molten ES was started.
  • the average molten ES addition time was under 2 minutes for 30% molten ES.
  • Ground phosphate rock, a dispersion of elemental sulphur in phosphoric acid, defoamer and water were fed to an agitated premixing tank.
  • Fertilizers were prepared from a range of dispersions (prepared as outlined above) having sulphur content from 10 to 30 wt.%, based upon the weight of the dispersion.
  • the ground phosphate rock was metered using an AccuRate feeder, and a vibratory trough feeder conveyed the phosphate rock to a premixing tank.
  • a peristaltic pump was used to feed the defoamer.
  • the dispersion of elemental sulphur in phosphoric acid was pumped from a day tank to the premixing tank and was measured using a magnetic flow meter. The premixing tank overflowed by gravity directly into the reactor.
  • the reactor was equipped with a variable-speed agitator fitted with three axial-flow downward thrust turbines. A constant level was maintained in the reactor; the calculated working volume was 231 liters. To achieve the target slurry temperature in the reactor (about
  • live steam was fed into the reactor through a pipe positioned at the same level as the bottom turbine on the agitator shaft.
  • the residence time in the reactor was approximately 100 minutes.
  • An exhaust fan was used to remove the reactor gases through a spray-type scrubber to clean gases before exhausting them into the atmosphere.
  • Water was used as the scrubbing medium.
  • Part of the scrubber liquor was directed to the reactor to control the density of the slurry.
  • the scrubber liquor for process control was metered and fed by gravity into the top of the reactor. The flow rate was manually checked.
  • the slurry from the reactor overflowed by gravity into a deep insulated cone and was transferred to a drum granulator by a positive-displacement, lobe-type, variable-speed pump.
  • a long drilled stainless steel pipe with six 6 mm holes was used to distribute the slurry onto a rolling bed of recycle material in the drum granulator .
  • a 15 cm retaining dam was located 61 cm from the discharge end of the granulator.
  • Gases drawn from the granulator area were treated with a venturi-type scrubber.
  • the scrubbing system used water as the scrubbing media.
  • Moist granular material from the granulator was discharged by gravity into a rotary dryer.
  • the dryer was operated with co-current airflow and heated using a propane-fired combustion chamber located directly in line with the material inlet of the dryer.
  • the operating temperature of the dryer was controlled indirectly by measuring the temperature of the air at the dryer discharge and adjusting the burner accordingly. During this activity, the dryer was operated at a rotational speed of 7 rpm.
  • a cyclone-type dust collector was located in the process air duct between the dryer discharge and the exhaust fan.
  • An open-wheel centrifugal fan discharged the exhaust air into the atmosphere.
  • a centrifugal-type bucket elevator transferred the material from the dryer discharge to an inclined double- deck, mechanically vibrated screen system.
  • the screen housing was fitted with a Ty-Rod oversize screen (4.00 mm opening) and a Ty-Rod undersize screen (2.36 mm opening) to produce a product material between 2.36 mm and 4.00 mm.
  • Oversize material from the screen system was routed to a chain mill.
  • the crushed material discharging from the chain mill was returned to the screen system.
  • Undersize material from the screen system was returned to the granulator together with a controlled fraction of the product size material to maintain optimum granulation.
  • the product-size fraction from the screen system was fed to a rotary cooler that was operated with co-current airflow.
  • the plant was equipped with a fugitive dust collection system.
  • An open-wheel centrifugal fan discharged the exhaust air into the atmosphere.
  • Product-size material was collected in portable hoppers and later stored in 1-mt supersacks.
  • Table 2 shows the ratio of the amount of elemental sulphur in the dust to the amount of elemental sulphur in the fertilizer product, for both dust streams. Ratios are shown for the process of preparing elemental-sulphur containing triple superphosphate fertilizer according to the invention, and also for a comparative process wherein commercial powdered sulphur was used instead of the dispersion of elemental sulphur in phosphoric acid prepared using a dispersion mill. A range of ratios are given to show the results for a number of product runs: Table 2
  • the ratios prefferably be as low as possible because dust containing high concentrations of elemental sulphur are potentially explosive.
  • the process of the present invention enables the skilled person to incorporate higher levels of sulphur in the fertilizer product without compromising safety.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Fertilizers (AREA)

Abstract

Cette invention concerne un procédé de fabrication d’un engrais contenant du soufre élémentaire. Ce procédé fait intervenir un broyeur à dispersion dans lequel un rotor tourne dans un stator à fentes pour humidifier du soufre élémentaire dans un liquide (de préférence un liquide aqueux) et obtenir ainsi une dispersion de soufre élémentaire moulu dans le liquide. Cette dispersion est combinée à d’autres composants pour donner un mélange de soufre et d’autres composants, lequel mélange est granulé dans une unité de granulation pour donner un engrais contenant du soufre élémentaire granulé.
PCT/EP2010/052042 2009-05-07 2010-02-18 Procédé de fabrication d’un engrais contenant du soufre élémentaire WO2010058038A1 (fr)

Priority Applications (10)

Application Number Priority Date Filing Date Title
US13/319,230 US8679219B2 (en) 2009-05-07 2010-02-18 Process for preparing an elemental sulphur-containing fertilizer
EP10704154.3A EP2429975B1 (fr) 2009-05-07 2010-02-18 Procédé pour la préparation d'un fertilisant contenant du soufre élémentaire
MA34425A MA33344B1 (fr) 2009-05-07 2010-02-18 Procédé de fabrication d'un engrais contenant du soufre élémentaire
NZ596251A NZ596251A (en) 2009-05-07 2010-02-18 Process for preparing an elemental sulphur-containing fertilizer
MX2011011823A MX2011011823A (es) 2009-05-07 2010-02-18 Proceso para preparar un fertilizante que contiene azufre elemental.
BRPI1011638-9A BRPI1011638B1 (pt) 2009-05-07 2010-02-18 Processo para preparar um fertilizante contendo enxofre elementar
CN2010800265110A CN102459130A (zh) 2009-05-07 2010-02-18 制备含元素硫的肥料的方法
AU2010202235A AU2010202235B2 (en) 2009-05-07 2010-02-18 Process for preparing an elemental sulphur-containing fertilizer
IL216111A IL216111A0 (en) 2009-05-07 2011-11-03 Process for preparing an elemental sulphur-containing fertilizer
TNP2011000556A TN2011000556A1 (en) 2009-05-07 2011-11-03 Process for preparing an elemental sulphur-containing fertilizer

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP09159679.1 2009-05-07
EP09159679 2009-05-07

Publications (1)

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WO2010058038A1 true WO2010058038A1 (fr) 2010-05-27

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US (1) US8679219B2 (fr)
EP (1) EP2429975B1 (fr)
CN (2) CN105060942B (fr)
AU (1) AU2010202235B2 (fr)
BR (1) BRPI1011638B1 (fr)
IL (1) IL216111A0 (fr)
MA (1) MA33344B1 (fr)
MX (1) MX2011011823A (fr)
NZ (1) NZ596251A (fr)
TN (1) TN2011000556A1 (fr)
WO (1) WO2010058038A1 (fr)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013083798A1 (fr) * 2011-12-08 2013-06-13 Shell Internationale Research Maatschappij B.V. Composition d'asphalte
WO2014009326A1 (fr) * 2012-07-09 2014-01-16 Shell Internationale Research Maatschappij B.V. Procédé pour la préparation d'une émulsion de particules de soufre élémentaire
RU2577888C1 (ru) * 2014-12-26 2016-03-20 Федеральное государственное бюджетное образовательное учреждение высшего образования "Тверской государственный университет" Способ утилизации на аммофос отработанной фосфорной кислоты после антикоррозионной обработки черных металлов
WO2017037262A1 (fr) * 2015-09-04 2017-03-09 Shell Internationale Research Maatschappij B.V. Engrais à base d'urée-nitrate d'ammonium
US10221106B2 (en) 2014-07-28 2019-03-05 Shell Oil Company Process for preparing a urea-sulphur fertiliser
US10464855B2 (en) 2014-01-09 2019-11-05 Shell Oil Company Process for preparing a urea-sulphur fertilizer
DE102018005069A1 (de) 2018-06-26 2020-01-02 Skw Stickstoffwerke Piesteritz Gmbh Verfahren zur Herstellung von harnstoffbasierten Düngemitteln mit elementaren Schwefel und Produkte davon
RU2769505C1 (ru) * 2018-05-10 2022-04-01 Арун Виттхал САВАНТ Новая питающая и обогащающая композиция для сельскохозяйственных культур

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9278858B2 (en) 2009-03-09 2016-03-08 Sulvaris Inc. Micronized sulphur powder and method of production of same
CA2821909A1 (fr) * 2012-07-27 2014-01-27 Carbon Basis Company Ltd. Produits de biocharbon et procede de fabrication de ceux-ci
US8801827B2 (en) * 2012-10-22 2014-08-12 Tiger-Sul Products (Canada) Co. Fertilizer composition containing sulfur and boron
TR201607901T1 (tr) * 2014-01-31 2017-05-22 Reliance Industries Ltd Gübre ürünleri.
CN107001165B (zh) * 2014-12-19 2021-05-11 国际壳牌研究有限公司 用于制备含硫土壤改进剂的方法
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CN108138028A (zh) 2015-10-08 2018-06-08 碳基有限公司 生物炭产品及其制造方法
EP3309137A1 (fr) * 2016-10-13 2018-04-18 YARA International ASA Composition améliorée à base d'urée comprenant du soufre élémentaire et son procédé de fabrication
US10519072B2 (en) 2017-02-23 2019-12-31 Produquímica Indústria E Comércio S.A. Multi-nutrient granular fertilizer compositions and methods of using the same
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US11180424B1 (en) 2018-12-07 2021-11-23 Fertile Peat Products, Llc Phosphate fertilizer with finely ground elemental sulfur, swelling agent and rock phosphate
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RU2744183C1 (ru) * 2020-05-26 2021-03-03 Общество с ограниченной ответственностью инновационное предприятие "Сульфидные технологии" Способ получения серосодержащего удобрения из отходов производства полисульфида кальция и полученное указанным способом удобрение
CN111606739A (zh) * 2020-06-17 2020-09-01 云南磷化集团海口磷业有限公司 一种含硫富过磷酸钙生产装置和制备方法

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE183147C (fr) *
US3177062A (en) * 1963-06-17 1965-04-06 Tennessee Valley Authority Process of making a granulated, homogeneous phosphate rock sulfur fertilizer
US4372872A (en) 1981-02-17 1983-02-08 Union Oil Company Of California Sulfur suspensions
NZ213682A (en) 1985-10-02 1988-11-29 New Zealand Fertilizer Manufac Dispersing sulphur in a liquid for use as a fertiliser
US5522553A (en) 1994-09-29 1996-06-04 Kady International Method and apparatus for producing liquid suspensions of finely divided matter
WO2004043878A1 (fr) 2002-11-14 2004-05-27 Shell Internationale Research Maatschappij B.V. Procede de fabrication de fertilisants a base de phosphate d'ammonium renfermant du soufre
WO2008089568A1 (fr) 2007-01-25 2008-07-31 Sulphur Solutions Procédé de broyage destiné à microniser le soufre

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101302122A (zh) * 2008-06-13 2008-11-12 云南云天化国际化工股份有限公司 一种含硫磷酸二铵肥料及其生产方法

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE183147C (fr) *
US3177062A (en) * 1963-06-17 1965-04-06 Tennessee Valley Authority Process of making a granulated, homogeneous phosphate rock sulfur fertilizer
US4372872A (en) 1981-02-17 1983-02-08 Union Oil Company Of California Sulfur suspensions
NZ213682A (en) 1985-10-02 1988-11-29 New Zealand Fertilizer Manufac Dispersing sulphur in a liquid for use as a fertiliser
US5522553A (en) 1994-09-29 1996-06-04 Kady International Method and apparatus for producing liquid suspensions of finely divided matter
WO2004043878A1 (fr) 2002-11-14 2004-05-27 Shell Internationale Research Maatschappij B.V. Procede de fabrication de fertilisants a base de phosphate d'ammonium renfermant du soufre
EP1560801B1 (fr) * 2002-11-14 2007-05-16 Shell Internationale Researchmaatschappij B.V. Procede de fabrication de fertilisants a base de phosphate d'ammonium renfermant du soufre
WO2008089568A1 (fr) 2007-01-25 2008-07-31 Sulphur Solutions Procédé de broyage destiné à microniser le soufre

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
"Perry's Chemical Engineers' Handbook", 1997
BOSWELL C C ET AL: "The effects of different manufacturing techniques on the availability of sulfate to pasture from mixtures of elemental sulfur with either triple superphosphate or partially acidulated reactive phosphate rock", FERTILIZER RESEARCH, KLUWER ACADEMIC PUBLISHERS, DORDRECHT, NL, vol. 44, no. 3, 1 January 1996 (1996-01-01), pages 255 - 263, XP008108025, ISSN: 0167-1731 *
BOSWELL ET AL., FERTILIZER RESEARCH, vol. 35, 1993, pages 127 - 149
WATKINSON ET AL., FERTILIZER RESEARCH, vol. 35, 1993, pages 115 - 126
YALCIN ET AL., POWDER TECHNOLOGY, vol. 146, 2004, pages 193 - 199

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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EA028496B1 (ru) * 2012-07-09 2017-11-30 Шелл Интернэшнл Рисерч Маатсхаппий Б.В. Способ получения эмульсии из частиц элементарной серы
WO2014009326A1 (fr) * 2012-07-09 2014-01-16 Shell Internationale Research Maatschappij B.V. Procédé pour la préparation d'une émulsion de particules de soufre élémentaire
CN104583157A (zh) * 2012-07-09 2015-04-29 国际壳牌研究有限公司 制备单质硫粒子的乳液的方法
US9598322B2 (en) 2012-07-09 2017-03-21 Shell Oil Company Process for preparing an emulsion of elemental sulphur particles
AU2016210632B2 (en) * 2012-07-09 2017-10-19 Shell Internationale Research Maatschappij B.V. Process for preparing an emulsion of elemental sulphur particles
US10464855B2 (en) 2014-01-09 2019-11-05 Shell Oil Company Process for preparing a urea-sulphur fertilizer
US10221106B2 (en) 2014-07-28 2019-03-05 Shell Oil Company Process for preparing a urea-sulphur fertiliser
RU2577888C1 (ru) * 2014-12-26 2016-03-20 Федеральное государственное бюджетное образовательное учреждение высшего образования "Тверской государственный университет" Способ утилизации на аммофос отработанной фосфорной кислоты после антикоррозионной обработки черных металлов
CN107922281A (zh) * 2015-09-04 2018-04-17 国际壳牌研究有限公司 尿素硝酸铵肥料
WO2017037262A1 (fr) * 2015-09-04 2017-03-09 Shell Internationale Research Maatschappij B.V. Engrais à base d'urée-nitrate d'ammonium
RU2769505C1 (ru) * 2018-05-10 2022-04-01 Арун Виттхал САВАНТ Новая питающая и обогащающая композиция для сельскохозяйственных культур
DE102018005069A1 (de) 2018-06-26 2020-01-02 Skw Stickstoffwerke Piesteritz Gmbh Verfahren zur Herstellung von harnstoffbasierten Düngemitteln mit elementaren Schwefel und Produkte davon

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US8679219B2 (en) 2014-03-25
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