Process for the production of potassium sulphate and magnesium sulphate from carnallite and sodium sulphate

Information

  • Patent Grant
  • 11306033
  • Patent Number
    11,306,033
  • Date Filed
    Friday, December 15, 2017
    6 years ago
  • Date Issued
    Tuesday, April 19, 2022
    2 years ago
Abstract
According to some embodiments there is provided a process for the recovery of SOP from Sulphate bearing mineral and Carnallite or Sylvenite, comprising: Dissolving Carnallite in water to obtain Sylvenite and high Magnesium Chloride brine; Adding Sodium Sulphate to said Carnallite to produce mixture of Kainte\Leonite, KCl and NaCl precipitant and brine containing Mg Cl2, KCl, NaCl; Separating the NaCl from the mixture; Obtaining a precipitant mixture of Leonite with KCl; Filtering said Leonite and washing with water to yield pure mixture of Leonite with KCl; Adding KCl to the Leonite with the KCl; and Decompose said Leonite with the KCl to SOP.
Description
FIELD OF THE INVENTION

The present invention relates to the field of fertilizers derived from any material of natural or synthetic origin that is applied to soils or to plant tissues to supply one or more plant nutrients essential to the growth of plants, specifically to production of potassium sulphate which is a key ingredient in the fertilizer industry.


BACKGROUND OF THE INVENTION

To grow properly, plants need nutrients (nitrogen, potassium, calcium, zinc, magnesium, iron, manganese, etc.) which normally can be found in the soil. Sometimes fertilizers are needed to achieve a desired plant growth as these can enhance the growth of plants.


This growth of plants is met in two ways, the traditional one being additives that provide nutrients. The second mode by which some fertilizers act is to enhance the effectiveness of the soil by modifying its water retention and aeration. Fertilizers typically provide, in varying proportions, three main macronutrients:


Nitrogen (N): leaf growth;


Phosphorus (P): Development of roots, flowers, seeds, fruit;


Potassium (K): Strong stem growth, movement of water in plants, promotion of flowering and fruiting;


three secondary macronutrients: calcium (Ca), magnesium (Mg), and sulphur (S);


micronutrients: copper (Cu), iron (Fe), manganese (Mn), molybdenum (Mo), zinc (Zn), boron (B), and of occasional significance there are silicon (Si), cobalt (Co), and vanadium (V) plus rare mineral catalysts.


The most reliable and effective way to make the availability of nutrients coincide with plant requirements is by controlling their release into the soil solution, using slow release or controlled release fertilizers.


Both slow release fertilizers (SRF) and controlled release fertilizers (CRF) supply nutrients gradually. Yet, slow release fertilizers and controlled release fertilizers differ in many ways: The technology they use, the release mechanism, longevity, release controlling factors and more.


Solid fertilizers include granules, prills, crystals and powders. A prilled fertilizer is a type of granular fertilizer that is nearly spherical made by solidifying free-falling droplets in air or a fluid medium. Most controlled-release fertilizers (CRFs) used in commercial nurseries are prilled fertilizers that have been coated with sulfur or a polymer. These products have been developed to allow a slow release of nutrients into the root zone throughout crop development.


Amongst the various fertilizers there is a dominant use of potassium sulfate. K2SO4 does not contain chloride, which can be harmful to some crops. Potassium sulfate is preferred for these crops, which include tobacco and some fruits and vegetables. Crops that are less sensitive may still require potassium sulfate for optimal growth if the soil accumulates chloride from irrigation water.


SUMMARY OF THE INVENTION

According to some demonstrative embodiments, there is provided a process for the production Potassium Sulphate (SOP) and Potassium Magnesium Sulphate as a product of reaction between Carnallite (KClMgCl2*6H2O) and Sodium Sulphate bearing minerals.


According to some embodiments, the process may include recovery of SOP from Sulphate bearing mineral and Carnallite and/or Sylvenite.


According to some embodiments, the process of the present invention may include the following steps:


Dissolving Carnallite in water to obtain Sylvenite and high Magnesium Chloride brine;


Adding Sodium Sulphate in various proportion to Carnallite, e.g., weight ratio Carnalite to Sodium Sulphate 14:3, to produce mixture of Kainte\Leonite, KCl and NaCl precipitant and brine containing MgCl2, KCl, NaCl, e.g., in equilibrium with the solid;


Separating the NaCl from the mixture, e.g., by flotation method or


Obtaining a precipitant mixture of Leonite with KCl,


Filtering the Leonite and washing with water to yield pure mixture of Leonite with KCl;


Adding proper quantity of KCl to the Leonite with the KCl, i.e., a sufficient quantity to convert Leonite to K2SO4, e.g., weight proportion of Leonite to Potash 3.5:5;


Decompose the Leonite with the KCl to SOP in Crystallizer.


Separating the crude SOP, e.g., using by filtration and/or centrifugation; and


Washing the SOP with water to appropriate grade, e.g., 93-96% K2SO4.


According to some embodiments, the final SOP may be dried and packaged according to methods known in the art.


According to some demonstrative embodiments the process may include selecting a specific ratio of Water\Carnallite, for example, a ratio of Carnallite to water 2.9:1.7 w/v, to lead to Carnallite decomposition and to MgCl2 brine saturated with KCl.


According to some embodiments, the water may decompose the Carnallite to brine containing MgCl2, KCl and NaCl. According to some embodiments, a minimum quantity of water may dissolve all the above mentioned salts.


According to some embodiments, the process may further include a reaction between a Sulphate anion from a Sulphate mineral coming in contact with the brine thereby producing Kainite, Leonite, and Shenite.


According to some embodiments, the process may further include a reaction between the Carnallite and the Sodium Sulphate to produce mixture of Kainite/Leonite KCl and NaCl.


According to some embodiments, the process may include further separation of the NaCl from the solids of the mixture, for example, by flotation.


According to some embodiments, the process may include addition of water to results in Leonite decomposing to SOP.







DETAILED DESCRIPTION OF THE INVENTION

According to some demonstrative embodiments, there is provided a process for the production Potassium Sulphate (SOP) and Potassium Magnesium Sulphate as a product of reaction between Carnallite (KClMgCl2*6H2O) and Sodium Sulphate bearing minerals.


According to some embodiments, the process may preferably be used in salt water lakes and/or brines.


According to some embodiments, the process may include recovery of SOP from Sulphate bearing mineral and Carnallite and/or Sylvenite.


According to some embodiments, the process of the present invention may include the following steps:


Dissolving Carnallite in water to obtain Sylvenite and high Magnesium Chloride brine;


Adding Sodium Sulphate in various proportion to Carnallite to produce mixture of Kainte\Leonite, KCl and NaCl precipitant and brine containing MgCl2, KCl, NaCl, e.g., in equilibrium with the solid;


Separating the NaCl from the mixture;


Obtaining a precipitant mixture of Leonite with KCl, e.g., by flotation method;


Filtering the Leonite and washing with water to yield pure mixture of Leonite with KCl;


Adding proper quantity of KCl to the Leonite with the KCl;


Decompose the Leonite with the KCl to SOP in Crystallizer.


Separating the crude SOP, e.g., using by filtration and/or centrifugation; and


Washing the SOP with water to appropriate grade.


According to some embodiments, the final SOP may be dried and packaged according to methods known in the art.


According to some demonstrative embodiments the process may include selecting a specific ratio of Water\Carnallite to lead to Carnallite decomposition and to MgCl2 brine saturated with KCl. According to some embodiments, the process may further include a reaction between a Sulphate anion from a Sulphate mineral coming in contact with the brine thereby producing Kainite, Leonite, and Shenite.


According to some embodiments, the process may further include a reaction between the Carnallite and the Sodium Sulphate to produce mixture of Kainite\Leonite KCl and NaCl.


According to some embodiments, the process may include further separation of the NaCl from the solids of the mixture, for example, by flotation.


According to some embodiments, the process may include addition of water to results in Leonite decomposing to SOP.


According to some embodiments, the decomposition of Leonite to SOP can also be carried out by adding only water, which will yield SOP and Magnesium Sulphate brine.


According to some demonstrative embodiments, Magnesium Sulphate salt can also produce from the above referenced brine.


EXAMPLES
Examples—1

2000 gr of Carnallite containing 5% NaCL and 5% adhering moisture mixed at 35° C. with 1200 gr of water. The suspension has been stirred for 1 hour. 142 gr of Na2SO4 has been added and stirring continue for 120 minutes at 35° C. The result suspension was separate and the solid 490 gr and the brine sent to analysis.


Solid composition in wt %:


NaCl—20.5


KCl—58.7


Kainite—20.8


Brine composition in mol/1000 mol H2O:


Na2Cl2—10.2


K2Cl2—9.8


MgSO4 7.7


MgCl2—50.2.


Example—2

2000 gr of Carnallite 5% NaCl 5% adhering moisture mixed at 35° C. with 1200 gr of water. The suspension has been stirred for 1 hour. 284 gr of Na2SO4 has been added and stirring continue for 120 minutes at 35° C. The result suspension was separate and the solid 608 gr and the brine sent to analysis.


Solid composition in wt %:


NaCl—33.6


KCl—43.3


Leonite—23.1


Brine composition in mol/1000 mol H2O:


Na2Cl2—10.9


K2Cl2—10.8,


MgSO4—13.1


MgCl2—46.5.


Example—3

2000 gr of Carnallite 5% NaCl 5% adhering moisture mixed at 35° C. with 1200 gr of water. The suspension has been stirred for 1 hour. 426 gr of Na2SO4 has been added and stirring continue for 120 minutes at 35° C. The result suspension was separate and the solid 811 gr and the brine sent to analysis.


Solid composition in wt %:


NaCl—42.7


KCl—25.3


Leonite—32.


Brine composition in mol/1000 mol H2O:


Na2Cl2—11.5


K2Cl2—11.4


MgSO4—19.3


MgCl2—40.3.


Example—4

2000 gr of Carnallite 5% NaCl 5% adhering moisture mixed at 35° C. with 1200 gr of water. The suspension has been stirred for 1 hour. 568 gr of Na2SO4 has been added and stirring continue for 120 minutes at 35° C. The result suspension was separate and the solid 811 gr and the brine sent to analysis.


Solid composition in wt %:


NaCl—42.8


KCl—10


Leonite—47.2.


Brine composition in mol/1000 mol H2O:


Na2Cl2—14.3


K2Cl2—12.4


MgSO4—18.4


MgCl2—36.3


Example—5

2778 gr of Carnallite was added to 8580 gr of brine with a composition of:


21.6 Na2Cl2


10.57 K2Cl2


14.91 MgSO4


23.16 MgCl2


the resulting suspension was mixed for 30 minutes.


1440 gr of Na2SO4 were gradually added in three steps.


The suspension was mixed for 30 minutes after each step.


The suspension was then mixed for additional 30 minutes and then pumped directly to Denver D-10 flotation cell and the NaCl was floated. The product composition contained 1367 gr of Leonite and 248 gr of NaCl.


Example—6

The same process of example 5 was applied with regard to mixing of 2778 gr of Carnallite with a brine having a composition of:


21.6 Na2Cl2


10.57 K2Cl2


14.91 MgSO4


23.16 MgCl2.


The final resulting product contained: 1351 gr of Leonite and 297.4 gr NaCl.


While this invention has been described in terms of some specific examples, many modifications and variations are possible. It is therefore understood that within the scope of the appended claims, the invention may be realized otherwise than as specifically described.

Claims
  • 1. A process for the recovery of SOP from sulphate bearing mineral carnallite, comprising: dissolving said carnallite in water to obtain sylvenite and high magnesium chloride brine;adding sodium sulphate to said dissolved carnallite to produce mixture of kainite\leonite, KCl and NaCl precipitant and brine containing MgCl2, KCl, NaCl;separating the NaCl from the mixture;obtaining a precipitant mixture of leonite with KCl;filtering said leonite and washing with water to yield pure mixture of leonite with KCl;adding KCl to the leonite with the KCl; anddecomposing said leonite with the KCl to SOP.
  • 2. The process of claim 1, wherein said SOP is separated from said mixture using a method selected from the group including filtration and centrifugation.
  • 3. The process of claim 2, wherein said SOP is further washed with water to yield an appropriate grade.
  • 4. The process of claim 3, wherein said SOP is further dried and packaged.
  • 5. The process of claim 1, wherein said sodium sulphate is added in a proportion to said dissolved carnallite to yield said mixture of kainite\leonite.
  • 6. The process of claim 1, wherein said precipitant mixture of leonite with KCl is obtained by a floatation method.
  • 7. The process of claim 1, wherein said leonite with the KCl is decomposed to SOP in a crystallizer.
PCT Information
Filing Document Filing Date Country Kind
PCT/IL2017/051354 12/15/2017 WO 00
Publishing Document Publishing Date Country Kind
WO2018/109773 6/21/2018 WO A
US Referenced Citations (53)
Number Name Date Kind
2136996 Wiedbrauck Nov 1938 A
2138827 Bailey Dec 1938 A
2997171 Samsel Aug 1961 A
3043652 Schytil Jul 1962 A
3332470 Chirico Jul 1967 A
3332827 Griffith Jul 1967 A
3532621 Hough Oct 1970 A
3548046 Savage Dec 1970 A
3711254 McGowan Jan 1973 A
3876387 Coulson Apr 1975 A
3877920 Carlberg Apr 1975 A
4068718 Cooke, Jr. Jan 1978 A
4129642 Neitzel Dec 1978 A
4283423 Watkins Aug 1981 A
4427068 Fitzgibbon Jan 1984 A
4963231 Ryham Oct 1990 A
5112379 Young May 1992 A
5174804 Rehberg Dec 1992 A
5651888 Shimizu Jul 1997 A
6284278 Waldman Sep 2001 B1
6287496 Lownds Sep 2001 B1
6454979 Phinney Sep 2002 B1
9592514 Kaps Mar 2017 B2
20020109736 Chailleux Aug 2002 A1
20020121117 Hartmann Sep 2002 A1
20040139992 Murkute Jul 2004 A1
20050072724 Nakayama Apr 2005 A1
20050276905 Xing Dec 2005 A1
20060003893 Taylor Jan 2006 A1
20060144789 Cath Jul 2006 A1
20060148646 Taylor Jul 2006 A1
20080223098 Taulbee Sep 2008 A1
20090261040 Pruet Oct 2009 A1
20090272692 Kurth Nov 2009 A1
20100213129 Jones Aug 2010 A1
20100224476 Cath Sep 2010 A1
20110017666 Cath Jan 2011 A1
20110064853 Maeki Mar 2011 A1
20110123420 Phinney May 2011 A1
20110257788 Wiemers Oct 2011 A1
20110315632 Freije, III Dec 2011 A1
20130001162 Yangali-Quintanilla Jan 2013 A1
20130264260 Heinzl Oct 2013 A1
20140001122 Schultz Jan 2014 A1
20140175011 Benton Jun 2014 A1
20140223979 Wiseman Aug 2014 A1
20140245803 Forsythe Sep 2014 A1
20140260467 Peacock Sep 2014 A1
20150014232 McGinnis Jan 2015 A1
20150101987 Yeh Apr 2015 A1
20160060182 Cook Mar 2016 A1
20170305805 Farnworth Oct 2017 A1
20180179117 Socolovsky Jun 2018 A1
Foreign Referenced Citations (93)
Number Date Country
102012031210 Jan 2015 BR
1076435 Sep 1993 CN
1083800 Mar 1994 CN
1091990 Sep 1994 CN
1093695 Oct 1994 CN
1236765 Dec 1999 CN
1297371 May 2001 CN
1314308 Sep 2001 CN
1387497 Dec 2002 CN
1407957 Apr 2003 CN
1485124 Mar 2004 CN
1548371 Nov 2004 CN
1690023 Nov 2005 CN
1715258 Jan 2006 CN
1793064 Jun 2006 CN
1997721 Jul 2007 CN
101608168 Dec 2009 CN
101772377 Jul 2010 CN
101792334 Aug 2010 CN
101844949 Sep 2010 CN
101993270 Mar 2011 CN
101993317 Mar 2011 CN
102001899 Apr 2011 CN
102304003 Jan 2012 CN
102304003 Jan 2012 CN
102464500 May 2012 CN
102464508 May 2012 CN
103011958 Apr 2013 CN
103688788 Apr 2014 CN
103930387 Jul 2014 CN
104016379 Sep 2014 CN
104211545 Dec 2014 CN
104341228 Feb 2015 CN
104609967 May 2015 CN
104609967 May 2015 CN
105130645 Dec 2015 CN
105263614 Jan 2016 CN
106082279 Nov 2016 CN
106495811 Mar 2017 CN
106536033 Mar 2017 CN
106536035 Mar 2017 CN
106699485 May 2017 CN
107418586 Dec 2017 CN
107922286 Apr 2018 CN
108367996 Aug 2018 CN
7200058 Feb 2015 CO
2408410 Aug 1974 DE
102007049182 May 2009 DE
102009041456 Mar 2011 DE
102013004597 Sep 2014 DE
0835161 Apr 1998 EP
0918045 May 1999 EP
2840074 Feb 2015 EP
2583412 Dec 1986 FR
935007 Aug 1963 GB
1378938 Dec 1974 GB
2514233 Nov 2014 GB
2522490 Jul 2015 GB
2522490 Jul 2015 GB
2522490 Dec 2015 GB
2577865 Apr 2020 GB
2577865 Apr 2020 GB
H0255397 Feb 1990 JP
2003112017 Apr 2003 JP
2004182549 Jul 2004 JP
3816870 Aug 2006 JP
101335445 Dec 2013 KR
695018 Jun 1982 SU
990756 Jan 1983 SU
990756 Jan 1983 SU
1574542 Jun 1990 SU
9629287 Sep 1996 WO
9629287 Sep 1996 WO
9730782 Aug 1997 WO
0121556 Mar 2001 WO
2006096825 Sep 2006 WO
2007071175 Jun 2007 WO
2009086587 Jul 2009 WO
2011053794 May 2011 WO
2012109723 Aug 2012 WO
2012115496 Aug 2012 WO
2013055219 Apr 2013 WO
2013055219 Apr 2013 WO
2014026048 Feb 2014 WO
2014181149 Nov 2014 WO
2015185907 Dec 2015 WO
2015185909 Dec 2015 WO
2016051130 Apr 2016 WO
2016178211 Nov 2016 WO
2018073815 Apr 2018 WO
2018109773 Jun 2018 WO
2018146684 Aug 2018 WO
2018154338 Aug 2018 WO
Non-Patent Literature Citations (61)
Entry
Bichara et al, FR 2583412, English Translation (Year: 1986).
Gao et al, CN 106082279, English Translation (Year: 2016).
Office Action data dated May 19, 2020 for U.S. Appl. No. 16/343,900 (pp. 1-6).
Office Action dated Apr. 7, 2020, for U.S. Appl. No. 16/343,900 (pp. 1-7).
Office Action dated Feb. 11, 2020, for U.S. Appl. No. 15/570,753 (pp. 1-9).
Office Action dated May 22, 2020 for U.S. Appl. No. 15/570,753 (pp. 1-11).
Bryan D. Coday et al., “The sweet spot of forward osmosis: Treatment of produced water, drilling wastewater, and other complex and difficult liquid streams” Desalination 333 (2014) 23-35.
Canadian Office Action dated Jul. 12, 2018 for corresponding CA Patent App. No. 2,890,360, 5 pages.
Extended European Search Report for Application No. 16789406.2 dated Dec. 14, 2018, 8 pages.
Indian Examination Report dated Jun. 28, 2018 for IN Application No. 829DELNP2015, 6 pages.
International Search Report and Written Opinion dated Dec. 19, 2013 for corresponding International Patent Application No. PCT/US2013/049166. 7 pages.
Office Action dated Jul. 3, 2018 for U.S. Appl. No. 15/559,424 (pp. 1-9).
Omeman, Z. et al., “Geopolymer cement in concrete: novel sustainable”, CEMENTO-HORMIGON , 78(906), 4-19 STNDatabase accession No. 2008:130694 XP002777656.
R. L. Earle., “Chapter 8: Evaporation. Multiple Effect Evaporation”, Unit Operations in Food Processing, (19831231), URL: http://www.nzifst.org.nz/unitoperations/evaporation2.htm, XP055282974, 18 pages.
RU Office Action dated Jul. 31, 2019 for RU Application No. 2017141009 (4 pages).
RU Office Action dated May 15, 2017 for RU Application No. 2015103308 (9 pages).
RU Search Report dated May 5, 2017 for RU Application No. 2015103308 (2 pages).
Russian Search Report for Application No. RU2017141009, dated Jul. 10, 2019, 2 pages.
Unit Operations in Food Processing—R. L Earle, 1983, NZIFST, http://www.nzifst.org.nz/unitoperations/evaporation2.htm. 7 pages.
Written Opinion of the International Search Authority for parent PCT application PCT/IL2016/050436, 6 pages.
Written Opinion of the International Search Authority for parent PCT application PCT/IL2017/050358 dated Jun. 25, 2017, 6 pages.
Written Opinion of the International Search Authority for parent PCT application PCT/IL2014/050278, dated Sep. 14, 2015. 6 pages.
Database WPI, Week 198346 Thomson Scientific, London, GB; AN 1983-819450, XP002801001, & SU 990 756 A (Kaluga Khlorvinil) Jan. 23, 1983 (Jan. 23, 1983) (1 page).
Extended European Search Report for App. No. EP18751114.2, dated Nov. 20, 2020, 8 pages.
Notice of Allowance dated Sep. 16, 2020 for U.S. Appl. No. 16/481,183 (pp. 1-9).
Office Action dated Aug. 25, 2020 for U.S. Appl. No. 16/343,900 (pp. 1-5).
Office Action dated Aug. 4, 2020 for U.S. Appl. No. 15/570,753 (pp. 1-13).
Office Action dated Sep. 25, 2020 for U.S. Appl. No. 16/343,900 (pp. 1-4).
Corrected Notice of Allowability dated Dec. 21, 2020 for U.S. Appl. No. 16/481,183 (pp. 1-2).
Office Action dated Jan. 12, 2021 for U.S. Appl. No. 16/343,900 (pp. 1-4).
Chile Office Action (with English translation) for App. No. CL02247-2019, dated Jan. 7, 2021, 16 pages.
Notice of Allowance dated Jan. 26, 2021 for U.S. Appl. No. 16/343,900 (pp. 1-5).
Brazilian Office Action (with English translation) for App. No. BR112019008082-1, dated Jul. 12, 2021, 8 pages.
Colombian Office Action for App. No. NC2019/0009684, dated Jun. 24, 2021, 6 pages.
Study on the phase change of gypsum in fertilizer salt and the granulation mechanism of compound fertilizer, Huanghua, Master's degree thesis of Shanxi Normal University Aug. 31, 2014, pp. 37-41.
ARIPO Search Report for App. No. AP/P/2019/011816, dated May 25, 2021, 4 pages.
Brazilian Office Action for App. No. BR112018007847-6, dated Apr. 22, 2021, 4 pages.
Chinese Office Action (with English translation) for App. No. CN2017800029016, dated Mar. 16, 2021, 28 pages.
Chinese Office Action (with English translation) for App. No. CN201780065167.8, dated May 28, 2021, 15 pages.
Corrected Notice of Allowability dated Feb. 19, 2021 for U.S. Appl. No. 16/343,900 (pp. 1-2).
English version of Chinese Office Action for App. No. CN2018800081429, dated May 24, 2021, 4 pages.
Indonesian Patent Office Action for App. No. PID201906345, dated Apr. 1, 2021, 4 pages.
Mu Changrong, et al., “Production and Application Technology of Compound Fertilizer”, Chengdu University of Science and Technology Press, Dec. 1994, 1st edition, p. 131, 4 pages.
Wu Yuguang et al., “Guide to the Use of Chemical Fertilizers”, China Agriculture Press, Sep. 2000, 1st edition, p. 112, 4 pages.
Xu Jinga, et al., “Series of Books on New Production Technology for Compound Fertilizer and Functional Fertilizer and Application Technology Thereof, Production Process Technology,” Chemical Industry Press, first edition, Sep. 2000, p. 84, 5 pages.
“Compendium of Polysulphate scientific research”, Potash House, P.O. Box 75, Beer-Sheva 8410001, Israel, www.polysulphate.com (Dec. 31, 2016) 88 pages.
Chinese Office Action (with English translation) in App. No. CN201780084381.8, dated Jul. 16, 2021, 11 pages.
Colombian Search Report for App. No. NC2019/0015080, dated Jun. 24, 2021, 7 pages.
Extended European Search Report for App. No. EP18817032.8, dated Feb. 25, 2021, 7 pages.
Indian Office Action for App. No. IN201927054628, dated Jun. 11, 2021, 6 pages.
Indonesian Office Action (with English translation) for App. No. P00202000013, dated Jul. 23, 2021, 7 pages.
Powder handling & processing, Compaction in Fertilizer Production, “Compaction-Granulation of Fertilizer. An Economical Process for a la carte Formulations”, vol. 11 (3), Jul./Sep. 1999 (Sep. 30, 1999) 4 pages.
Albadarin, Ahmad B. et al., “Granulated polyhalite fertilizer caking propensity”, Powder Technology, vol. 308, (Dec. 8, 2016), pp. 193-199, URL: https://doi.org/10.1016/j.powtec.2016.12.004, XP029890407.
Chinese Office Action (with English translation) for App. No. CN201880047533.1, dated Aug. 24, 2021, 10 pages.
English version of Chinese Office Action for App. No. CN2017800029016, dated Nov. 16, 2021, 12 pages.
ARIPO Search Report for App. No. AP/P/2019/011816, dated Nov. 14, 2021, 1 page.
Chinese Office Action (with English translation) for App. No. CN201780065167.8, dated Jan. 6, 2022, 8 pages.
Chinese Office Action (with English translation) for App. No. CN201880089257.5, dated Dec. 24, 2021, 16 pages.
Chinese Office Action (with English translation) for App. No. CN201980021914.7, dated Jan. 6, 2022, 10 pages.
European Patent Office Communication pursuant to Article 94(3) EPC for App. No. EP17801109.4, dated Dec. 1, 2021, 2 pages.
Examination Report for App. No. GB1909749.2, dated Jan. 10, 2022, 2 pages.
Related Publications (1)
Number Date Country
20190359535 A1 Nov 2019 US
Provisional Applications (1)
Number Date Country
62435760 Dec 2016 US