CA2762376A1 - Transition metal compound particles and methods of production - Google Patents

Abstract

A method of preparing insoluble transition metal compound particles is described, comprising: providing a transition metal salt at a concentration greater than 0.1 M wherein the transition metal component includes Mn, or Co; providing a source of a carbonate-, hydroxide-, phosphate-, oxyhydroxide- or oxide-based anionic compound at a concentration greater than 0.1 M wherein the anionic component is reactive with the transition metal component to form the particles; subjecting the transition metal salt and the anionic compound to sonication in a reaction chamber at an ultrasonic power density from about 0.1 to 50 W/mL to form particles.

Description

TRANSITION METAL COMPOUND PARTICLES
AND METHODS OF PRODUCTION
FIELD
[0001] The present disclosure relates generally to metal compound particles and methods of their production. More particularly, the present disclosure relates to transition metal compound particles and sonication-based methods of production.

.BACKGROUND

[0002] The control of particle size, morphology or both is important in some circumstances. Particles size can be affected after production of the particles using processes such as milling, but such processes may have a detrimental effect on the material properties. During precipitation or crystallization from solution, particle size, morphology or other properties may be controlled.

[0003] Crystallization or precipitation is achieved by mixing a solvent containing an active principal to be crystallized with an anti-solvent, so that after mixing the solution is supersaturated and crystallization occurs. Precipitation can also be achieved by the reaction of two or more reagents that form a product which has reduced solubility in the solvents being used. The resulting insoluble reaction product precipitates or crystallizes from the solution. In such a situation, the solvents being used in the reaction would be considered to be anti-solvents with respect to the reaction product. The term "anti-solvent"
means a fluid which promotes precipitation of the active principal from the solvent. The anti-solvent can be the same liquid as the solvent but at a different temperature, it may be a different liquid from the solvent, or (in the case of two reagents reacting to form a new product) it may be the solvent used in the reaction.

[0004] Ultrasonic irradiation (or sonication) has been used while precipitating or crystallizing particles. For example, Hussein OUBANI and others, in the Asia-Pacific Journal of Chemical Engineering 5 (2010) 599-608, describe the precipitation of NaCl microparticles from a NaCl - Ethanol - Water antisolvent system; L. BOELS and others, in the Journal of Crystal Growth 312 (2010) 961-966, describe the crystallization of a supersaturated calcite suspension under ultrasonic irradiation; and I.
NISHIDA, in Ultrasonics Sonochemistry 11 (2004) 423-428, describes the ultrasonic irradiation of a supersaturated solution of calcium carbonate.

[0005] Hielscher Ultrasonics produces ultrasonic devices and describes an ultrasonic precipitation process at <http://www.hielscher.com/ultrasonics/precipitation_01.htm>.

[0006] A poster presentation by B. POHL, N. OZYLIMAZ, G. BRENNER, and U.
PEUKER, entitled "Untersuchungen zur Optimierung von kontinuierlichen Ultraschalldurchflussreaktoren", publically available at least as early as December 20, 2010, describes how flow chamber size and geometry of ultrasonic reactors affect the formation of 13- and BaSO4.

[0007] A poster presentation by B. POHL, G. BRENNER, and U. PEUKER, entitled "Optimierung von Ultraschallfallungsreaktoren - kontrollierte Nanopartikelherstellung", publically available at least as early as December 20, 2010, teaches that ultrasonic precipitation reactors can be used to form agglomerations of Fe304 particles, where the agglomerates are between 20 nm and 300 nm (cavitation field reactor) or between 20 nm and 1 m (conical reactor).

[0008] A review article discussing the chemical effects of ultrasonic irradiation was authored by Kenneth SUSLICK in Science 247:4949 (1990) 1439-1445. Another review article, by G. RUECROFT and others in Organic Process Research &
Development, discusses the application of ultrasound to crystallization of organic molecules, and discusses equipment that could be used in industrial environments, such as parallel plate transducer systems.

[0009] Chunling LU and Jinglin ZHANG, in The Journal of the Chinese Ceramic Society 35:3 (2007) 377-380, describe subjecting a reaction of manganese sulfate (MnSO4) and ammonium bicarbonate (NH4HCO3) to ultrasonic irradiation, using an ultrasonic bath having an intensity of about 1 W/cm2, to form cubical manganese carbonate (MnCO3) particles from 400 to 500 rim.

[0010] Ting-Feng YI and Xin-Guo HU, in the Journal of Power Sources 167 (2007) 185-191, disclose preparing sub-micro spinel LiNi055-XMn155+,O4 (x <
0.1) cathode materials with homogeneous particle size using an ultrasonic-assisted co-precipitation of LiNO3, Mn(N03)2, and Ni(N03)2.6H20. The precipitation was sonicated at 80 C
for 5 h in an ultrasonic cleaner at 50W and 28 kHz.
[00111 Peizhi SHEN and others, in the Journal of Solid State Electrochemistry (2005) 10:929-933, describe preparing a LiCr,,Mn2_,,04 (x=0, 0.02, 0.05, 0.08, 0.10) compound with spinel crystal structure using an ultrasonic co-precipitation method.
Lithium acetate, manganese acetate, chromic nitrate and citric acid were dissolved in water and treated in an ultrasonic bath.
[00121 U.S. Patent App. No. 2010/0018853 describes the control of crystal and precipitate particle size of pharmaceutical drugs or other medicaments using ultrasonic irradiation.
[00131 Ultrasonic irradiation is also used in other processes for preparing particles.
Tingfeng YI, Xinguo HU and Kun GAO, in the Journal of Power Sources 162 (2006) 643, prepare Al-doped LiAlo.o5Mn1.9504 powders using an ultrasonic assisted sot-gel method, using adipic acid as a chelating agent. A sol-gel process is a wet-chemical technique used primarily for the fabrication of materials (typically a metal oxide) starting from a chemical solution (or sot) that acts as the precursor for an integrated network (or gel) of either discrete particles or network polymers. Stoichiometric amounts of reactants Li(CH3000)=2H2O, AI(NO3)3.9H2O and Mn(CH3000)2.6H2O were used to prepare the LiAlo.05Mn1.9504 powders.
[0014] S.H. PARK and others, in the Journal of Applied Electrochemistry (2003) 33: 1169-1173, describe the preparation of Li[Nili2Mnli2]O2 using an ultrasonic spray pyrolysis method. In spray pyrolysis, the dissolved reagents are atomized using an ultrasonic nebulizer and the resulting aerosol stream is introduced into a heated reactor.
They teach that stoichiometric amounts of Ni and Mn nitrate salts (cationic ratio of Ni:Mn - 1:1) were dissolved in water and that the dissolved solution was added to a continuously agitated aqueous citric acid solution, which was used as a polymeric agent for the reaction.
The starting solution was atomized using an ultrasonic nebulizer with a resonant frequency of 1.7 MHz and the aerosol stream was introduced into a reactor heated at 500 C.
100151 In a similar process, S.H. PARK and others, in Electrochimica Acta 49 (2004) 557-563, teach the preparation of Li[Ni1i3Coli3Mnti3102 materials using a spray pyrolysis method, where citric acid is again used as a polymeric agent for the reaction.

[00161 Spherical particles can be used in the preparation of battery materials, as discussed by SUN and others in Process of Precipitation for Spherical Manganese Carbonate and Their Products Produced Thereby (WO 2006/109940), as well as in the pharmaceutical industry. Weijun TONG and Changyou GAO, in Colloids and Surfaces A:
Physiochem Eng. Aspects 295 (2007) 233-238, describe the preparation of hollow spherical manganese carbonate capsules by the reaction of manganese sulfate and ammonium bicarbonate solutions to form manganese carbonate particles and then acid dissolution of the particle cores. Similarly, Alexei ANTIPOV and others, in Colloids and Surfaces A: Physiochem Eng. Aspects 224 (2003) 175-183, describe the formation of hollow capsules made using cadmium carbonate particles, manganese carbonate particles and calcium carbonate particles as core templates for adsorption of oppositely charged polyelectrolytes and subsequent core removal.
[00171 Although ultrasonic irradiation has been used during precipitation of metal compound particles, as described above, it is desirable to provide an ultrasonic irradiation-based method that allows for the production of particles with desired morphologies, desired size distribution and/or desired particle sizes.

SUMMARY
[0018] It is an object of the present disclosure to obviate or mitigate at least one disadvantage of previously described methods, systems and/or particles.
[0019] There is described herein a method of preparing insoluble transition metal compound particles in a reaction chamber, said particles represented by the formula (TM)(S'), the method comprising: providing a transition metal salt solution, the transition metal salt having the formula (TM)(S) and comprising transition metal component (TM) is one or more transition metal independently selected from the group consisting of Mn, Ni, Co, Mg, Zn, Ca, Sr, Cu, Zr, P, Fe, Al, Ga, In, Cr, Ge and Sri; providing source of an anionic compound, the anionic compound being a carbonate-, hydroxide-, phosphate-, oxyhydroxide- or oxide-based compound, said anionic compound comprising an anionic component represented by S', wherein said anionic component is reactive with the transition metal component TM to form the insoluble transition metal compound particles;
adding the transition metal salt solution and the anionic compound to a reaction chamber;

and subjecting the reaction chamber to sonication at an intensity of from about 0.1 W/mL
to about 50 W/mL to form the insoluble transition metal compound particles.
[0020] The intensity maybe from about 1 W/mL to about 10 W/mL. In some examples, the intensity may be about 3 W/mL.
[0021] The transition metal salt solution may include MnSO4, Mn(CH3COO)2, MnC12, or Mn(N03)2.
[0022] The source of the anionic compound may be a solution comprising Na2CO3, N114HCO3, (NH4)2CO3, NH4OH, NaHCO3, NaOH, KHCO3, K2C03, KOH, H3PO4, NaH2PO4, Na2HPO4, (NH4)3PO4, (NH4)2HP04, (NH4)H2PO4, (NH4)2NaPO4, (NH4)Na2PO4, KH2PO4, K2HPO4, (NH4)2KPO4, (`1114)K2PO4 or KMnO4. In some examples, the source of the anionic compound maybe a solution comprising Na2CO3 and/or NH4HCO3.
[0023] The ratio of the anionic compound to the transition metal salt in the reaction chamber may be from about 1:1.5 to about 1.5:1. In some examples, the ratio of the anionic compound to the transition metal salt in the reaction chamber may be about 1:1.

[0024] The sonication may be provided by a probe tip, by vibrating diaphragms, or by any number of ultrasonic transducers attached to reaction chamber walls.
[0025] The reaction chamber may include a flow-through or continuous chamber.
[0026] The insoluble transition metal compound particles may be spherical, quasi-spherical or irregular in shape.
[0027] The insoluble transition metal compound particles produced may have a particle size distribution of at least 90% of particles within 1 gm and 50 gm;
at least 90%
within 1 m and 30 m; at least 90% within 3 m and 20 gm; or at least 90%
within 3 m and 10 m.
[0028] The insoluble transition metal compound particles produced may include MnCO3 and have a tap density from about 1.5 g/mL to about 3.0 g/mL.
[0029] The insoluble transition metal compound particles produced may have a tap density from about 1.7 g/mL to about 2.3 g/mL.
[0030] The method may be performed where the transition metal salt solution comprises MnSO4, the source of the anionic compound is a solution comprising Na2CO3 and/or NH4HCO3, the ratio of MnSO4 to Na2CO3 and/or NH4HCO3 is from about 1:1.5 to about 1.5:1, and the particles include MnCO3 have a tap density of from about 1.7 g/mL to about 2.3 g/mL.
[0031] The volume of the reaction chamber may be 300 mL or greater. The transition metal salt solution and the anionic compound may be added to a reaction chamber via reagent entry ports positioned more than about 10 cm apart from each other.
[0032] The residence time in the reaction chamber may be from about 1 second to about 60 minutes, for example from about 5 seconds to about 30 minutes, or for example from about 10 seconds to about 5 minutes.
[0033] The method may also include adding a chelating agent to the reaction chamber. The chelating agent may be ammonium sulfate, ammonium hydroxide, ammonium chloride, ammonium acetate, ammonium nitrate, urea, or any mixture thereof.
[0034] Other aspects and features of the present disclosure will become apparent to those ordinarily skilled in the art upon review of the following description of specific embodiments in conjunction with the accompanying figures.

BRIEF DESCRIPTION OF THE DRAWINGS
[0035] Embodiments of the present disclosure will now be described, by way of example only, with reference to the attached Figures.
[0036] Figure 1 is a scanning electron microscope micrograph of manganese carbonate particles produced in a tank reactor.
[0037] Figure 2 is a scanning electron microscope micrograph of manganese carbonate particles produced in a tank reactor.
[0038] Figure 3 is a scanning electron microscope micrograph of the manganese carbonate particles shown in Figure 2, shown at a higher magnification.
[0039] Figure 4 is a scanning electron microscope micrograph of manganese carbonate particles produced in a continuous process reactor, without sonication.
[0040] Figure 5 is a scanning electron microscope micrograph of manganese carbonate particles produced in a continuous reactor, with sonciation, according to an aspect the present application.
[00411 Figure 6 is an illustration of a continuous process reactor according to one embodiment of the present application.

[0042] Figure 7 is a scanning electron microscope micrograph of manganese carbonate particles produced in a continuous process reactor, according to an aspect of the present application.
[0043] Figure 8 is a scanning electron microscope micrograph of manganese carbonate particles produced in a continuous process reactor, according to an aspect of the present application.
[0044] Figure 9 is a scanning electron microscope micrograph of manganese carbonate particles produced in a continuous process reactor, according to an aspect of the present application.

[0045] Figure 10 is a scanning electron microscope micrograph of the manganese carbonate particles shown in Figure 9, shown at a higher magnification.
[0046] Figure 11 is a scanning electron microscope micrograph of manganese carbonate particles produced in a continuous process reactor, according to an aspect of the present application.
[0047] Figure 12 is a scanning electron microscope micrograph of the manganese carbonate particles shown in Figure 11, shown at a higher magnification.
[0048] Figure 13 is a scanning electron microscope micrograph of manganese carbonate particles produced in a continuous process reactor, according to an aspect of the present application.
[0049] Figure 14 is a scanning electron microscope micrograph of manganese carbonate particles produced in a continuous process reactor, according to an aspect of the present application.
[0050] Figure 15 is a scanning electron microscope micrograph of manganese carbonate particles produced in a continuous process reactor, according to an aspect of the present application.
[0051] Figure 16 is a scanning electron microscope micrograph of nickel manganese cobalt (NMC) carbonate particles produced in a continuous process reactor, according to an aspect of the present application.
[0052] Figure 17 is a scanning electron microscope micrograph of NMC carbonate particles produced in a continuous process reactor, according to an aspect of the present application.

[00531 Figure 18 is a schematic representation of the precipitation that may occur when a reagent is present in excess.
[00541 Figure 19 is a schematic representation of the reaction when neither reactant is present in excess.
[00551 Figure 20 provides scanning electron microscope micrographs of particles produced with and without excess reagent.
[00561 Figure 21 illustrates exemplary particles obtained with a SEM
micrograph showing both a lower magnification (left) and a higher magnification (right).
[00571 Figure 22 is a scanning electron micrograph of manganese carbonate particles produced in a continuous reactor with no ultrasonic irradiation.
[00581 Figure 23 is a scanning electron micrograph of manganese carbonate particles produced in a continuous reactor, according to an aspect of the present application.
[00591 Figure 24 is a scanning electron micrograph of manganese carbonate particles produced in a continuous reactor, according to an aspect of the present application.
[0060] Figure 25 is a scanning electron micrograph of manganese carbonate particles produced in a continuous reactor, according to an aspect of the present application.
[00611 Figure 26 is a scanning electron micrograph of manganese carbonate particles produced in a continuous reactor, according to an aspect of the present application.
[00621 Figure 27 is a scanning electron micrograph of manganese carbonate particles produced in a continuous reactor, according to an aspect of the present application.
[00631 Figure 28 is a scanning electron micrograph of manganese carbonate particles produced in a continuous reactor, according to an aspect of the present application.
[00641 Figure 29 is a scanning electron micrograph of manganese carbonate particles produced in a continuous reactor, according to an aspect of the present application.

[00651 Figure 30 is a scanning electron micrograph of manganese carbonate particles produced in a continuous reactor, according to an aspect of the present application.

[00661 Figure 31 illustrates the particle size distribution plots for the samples illustrated in Figures 17 and 22-31 where panel A illustrates the particle size distribution of the sample shown in Figure 22, panel B illustrates the particle size distribution of the sample shown in Figure 23, panel C illustrates the particle size distribution of the sample shown in Figure 7, panel D illustrates the particle size distribution of the sample shown in Figure 24, panel E illustrates the particle size distribution of the sample shown in Figure 25, panel F illustrates the particle size distribution of the sample shown in Figure 17, panel G illustrates the particle size distribution of the sample shown in Figure 26, panel H
illustrates the particle size distribution of the sample shown in Figure 27, panel I illustrates the particle size distribution of the sample shown in Figure 28 , panel J
illustrates the particle size distribution of the sample shown in Figure 29, and panel K
illustrates the particle size distribution of the sample shown in Figure 30.

DETAILED DESCRIPTION
[0067] Generally, the present disclosure provides a method and system for producing particles having desired morphologies, desired size distribution and/or desired particle sizes. A particle's morphology refers to the shape of the particle.
For example, a precipitated or crystallized particle could be spherical, or quasi-spherical, cubic, or rod-like. Quasi-spherical particles refer to particles where not all particles are similarly shaped, but that the shape of most particles constitutes a shape that approaches a spherical shape without being perfectly spherical.
100681 It can be desirable to form spherical or quasi-spherical particles since powders that are composed of spherical or quasi-spherical particles can act more fluid-like and can exhibit less agglomeration under heating in comparison to irregularly shaped particles. Further, spherical or quasi-spherical particles can pack together to reduce void volume and increase tap density. Battery materials composed of spherical or quasi-spherical particles can perform better and can have a longer cycle life than batteries made using materials composed of irregular particles. Irregularly shaped particles have surfaces that are under stress due to sharp edges and folds, whereas spherical or quasi-spherical particles lack such sharp edges and folds, leading to reduced particle degradation. Particles can also be coated with other materials. Coatings made with spherical or quasi-spherical particles can be more uniform than coatings made with irregularly shaped particles. Even so, there may be applications in which irregularly shaped particles are desirable.
[0069] Particle size for a spherical precipitate can be defined by its diameter. With irregular and non-spherical particles, a volume-based particle size can be approximated by the diameter of a sphere that has the same volume as the non-spherical particle. Similarly, an area-based particle size can be approximated by the diameter of the sphere that has the same surface area as the non-spherical particle. The particle size for non-spherical particles can be calculated using other comparable properties, resulting in weight-based, hydrodynamic-based or aerodynamic-based particle sizes. In the present disclosure, particle size and volume-based particle size are used interchangeably.
[0070] The particle size distribution of a powder or particles dispersed in a fluid is a list of values that defines the relative amount of particles present, sorted according to size. Particle size distribution can be measured using a variety of techniques. Particle size distribution can be expressed in terms of a percentage of the sample between an upper limit and a lower limit, e.g. 80% of the sample between 10 m and 20 gm.
Alternatively, particle size distribution can be expressed in "cumulative" form, in which the total is given for all the sizes below an upper limit, e.g. 90% of the sample being less than 50 m.
[0071] The size of the precipitated particles, the morphology of the precipitated particles, and the particle size distribution of the precipitated particles all affect the tap density of a sample. Tap density refers to the density of a sample after tapping it sufficiently to compact the sample so that the sample's density no longer changes.
Depending on the size and shape of the particles produced, the tap density can be 10%, 20%, 30%, 40%, 50%, 60%, 70% or 80% of the crystal bulk density. Perfectly packed spheres of the same size could have a density of about 74% of the crystal bulk density, so perfectly packed spheres of MnCO3 could have a density of about 74% of 3.70 g/mL. It is conceivable for the density to be greater than 74% for a sample of spheres of various sizes whereby the gaps left by large particles are filled by smaller particles.
[0072] Particles can be obtained in a batch process or in a continuous process. In a continuous process, a "flow through" reactor is used where the produced particles are continuously removed from the reactor by the addition of new reagents. The particles can be transition metal compound particles represented by the general formula (TM)(S'), where TM can be one or more transition metals independently selected from the group consisting of Mn, Ni, Co, Mg, Zn, Ca, Sr, Cu, Zr, P, Fe, Al, Ga, In, Cr, Ge and Sn, in any possible molar ratio; and where S' is the anionic component of the transition metal compound particle. The anionic component S' of the transition metal compound particles can be, for example, C03, (OH)2, (OOH), 02, 03, 04, P04, (P04)2, or P207 resulting in the formula being, for example, (TM)C03, (TM)(OH)2, (TM)(OOH), (TM)O, (TM)02, (TM)03, (TM)03i2, (TM)04i3, (TM)P04, (TM)(P04)2/3, or (TM)(P207)1i2, depending on the overall valence charge of the TM component.
[00731 The transition metal component of the transition metal compound particles can come from a source of transition metal, for example a solution of a transition metal salt represented by the general formula (TM)(S) where S is any appropriate counter ion that allows the transition metal salt to dissolve in a solvent. Examples of such a transition metal salt include (TM)S04, (TM)C12, (TM)(CH3COO)2, and (TM)(N03)2 where S is SO4, C12, (CH3COO)2 and (NO3)2 respectively. The anionic component of the transition metal compound particle can come from any relevant source of anionic compound, for example another salt solution, such as a solution of NH4HCO3, Na2CO3, (NH4)2CO3, NH4OH, NaHCO3, NaOH, KHCO3, K2C03, KOH, H3PO4, NaH2PO4, Na2HPO4, (NH4)3PO4, (N-Ha)2HP04, (NH4)H2PO4, (NH4)2NaPO4, (NH4)Na2PO4, KH2PO4, K2HPO4, (NH4)2KPO4, (NH4)K2P04 or KMnO4.
[00741 In some embodiments, the transition metal compound particles can be Mn(l_ p_q) M2pM3gC03 particles (i.e. M' is Mn, S' = C03) where M2 and M3 are independently selected from the group consisting of Ni, Co, Mg, Zn, Ca, Sr, Cu, Zr, P, Fe, Al, Ga, In, Cr, Ge and Sn, where p + q < 1, and where "p" and "q" are greater than or equal to 0. In particular embodiments, the transition metal compound particles that can be obtained include nickel manganese cobalt (NMC) carbonate particles with the formula (NipMn(l_p_ q)Coq)CO3 (i.e. TM is NipMntl_p1)Coq where M' is Mn, M2 is Ni, M3 is Co, S' =
CO3), for example NMC carbonate particles having the formula Niv3Mn1i3Co1i3CO3. In other embodiments, the transition metal particles that can be obtained include manganese carbonate (MnCO3) particles (i.e. "p" and "q" = 0, S' = CO3).
[00751 Manganese carbonate particles can be formed through the reaction between manganese sulfate (MnSO4, i.e. TM = Mn, S = SO4) and ammonium bicarbonate

-11-ti (NH4HCO3), though other sources of manganese, for example Mn(N03)2, Mn(CH3COO)2, or MnC12, (where TM = Mn, S = (NO3)2, (CH3COO)2 or C12, respectively) and other sources of carbonate, for example Na2CO3i (NH4)2CO3, NaHCO3, KHCO3, or K2C03, can be used. Still other sources of manganese and carbonate are known in the art.
Although this disclosure discusses the reaction of manganese sulfate with ammonium bicarbonate to form manganese carbonate particles, and of manganese sulfate with sodium carbonate to form manganese carbonate particles, it is to be understood that alternative reagents could be similarly used to form alternative particles, such as Nili3Co2i3(OH)2 (where TM =
Nili3Co2i3, S' = (OH)2) or MgZnO3 (where TM = MgZn, S' = 03)-100761 The production of MnCO3 particles in a tank reactor using MnSO4 and NH4HCO3 at 1-2 M, or even higher concentrations, resulted in particles of up to 40 microns, with the produced particles having a large size distribution, as illustrated in Figure 1. A reaction using MnSO4 and NH4HC03 at 1 mM resulted in spherical particles approximately 3.5 microns, with the produced particles having a small size distribution, as illustrated in Figure 2 and Figure 3. Although the particle size, particle morphology and particle size distribution of the particles produced in Figure 2 and Figure 3 can be desirable, the low concentration of the reagents used can result in undesirable levels of waste.
[0077] Methods and systems according to the present application can produce spherical particles having desired physical properties using higher concentrations of reagents (for example at reagent concentrations of greater than: 100 mM, 1 M, 2 M, 3 M, 4 M, 5 M or 10 M, depending on the reagent) than similar methods and systems which do not use ultrasonic irradiation. Quick and intimate mixing is possible when using ultrasonic irradiation. The ratio of the reagent concentrations used in the reaction can be chosen depending on the desired product and the chemical reaction forming the transition metal compound particles. Any ratio, including an excess of one or more reagents with respect to another reagent, could be used in the formation of the transition metal compound particles.
In certain examples, it may be beneficial for no excess of reagents to be used.
[0078] The MnCO3 particles produced in a continuous reactor by the reaction of MnSO4 and NH4HCO3 at 0.2 M are shown in Figure 4 (no sonication) and Figure 5 (sonication using a 40 W ultrasonic cleaner). As illustrated by Figure 4 and Figure 5,

-12-ti sonication of the reaction solution results in individual grains being produced, while no sonication results in agglomerated particles.
[00791 A method of preparing insoluble transition metal compound particles in a reaction chamber is described herein. The particles formed are represented by the formula (TM)(S'). The method comprises providing a transition metal salt solution, the transition metal salt having the formula (TM)(S) and comprising transition metal component (TM) where (TM) is one or more transition metal independently selected from the group consisting of Mn, Ni, Co, Mg, Zn, Ca, Sr, Cu, Zr, P, Fe, Al, Ga, In; Cr, Ge and Sn;
providing source of an anionic compound, the anionic compound being a carbonate-, hydroxide-, phosphate-, oxyhydroxide- or oxide-based compound, said anionic compound comprising an anionic component represented by S', wherein said anionic component is reactive with the transition metal component TM to form the insoluble transition metal compound particles; adding the transition metal salt solution and the anionic compound to a reaction chamber; and subjecting the reaction chamber to sonication at an intensity of from about 0.1 W/mL to about 50 W/mL to form the insoluble transition metal compound particles.
[00801 The intensity may be from about 0.1 W/mL to about 10 W/mL, for example about 3 W/mL.
[0081] The transition metal salt solution may comprise MnSO4, Mn(CH3COO)2, MnC12, or Mn(N03)2.
[00821 The source of the anionic compound is a solution comprising Na2CO3, NH4HCO3, (NH4)2CO3, NH40H, NaHCO3, NaOH, KHCO3, K2CO3, KOH, H3PO4, NaH2PO4, Na2HPO4, (NH4)3PO4, (NH4)2HP04, (NH44)H2PO4, (NH4)2NaPO4i (NH4)Na2PO4, KH2PO4, K2HP04, (NH4)2KPO4, (NH4)K2PO4 or KMn04. In exemplary embodiments, the source of the anionic compound is a solution comprising Na2CO3 or NH4CO3.
[00831 An exemplary ratio of the anionic compound to the transition metal salt in the reaction chamber may be from about 1:1.5 to about 1.5:1, such as for example about 1:1.
[00841 Sonication may be provided by a probe tip, by vibrating diaphragms, or by any number of ultrasonic transducers attached to reaction chamber walls.
[00851 The reaction chamber may comprise a flow-through chamber.

-13-[0086] The insoluble transition metal compound particles may be generally spherical in shape, or may be quasi-spherical, meaning not all particles are similarly shaped, but that the shape of most particles constitutes a shape that approaches a spherical shape without being perfectly spherical.
[0087] In exemplary embodiments, the insoluble transition metal compound particles produced may have a particle size distribution of at least 90% of particles within 1 m and 50 m; at least 90% within 1 m and 30 m; at least 90% within 3 gm and 20 m; or at least 90% within 3 m and 10 gm.
[0088] According to certain embodiments, the insoluble transition metal compound particles produced may comprise MnCO3 and have a tap density from about 1.5 g/mL to about 3.0 g/mL. For example, the insoluble transition metal compound particles produced may have a tap density from about 1.7 g/mL to about 2.3 g/mL.
[0089] In certain embodiments, the transition metal salt solution may comprise MnSO4, the source of the anionic compound can be a solution comprising Na2CO3 and/or NH4CO3, the ratio of MnSO4 to Na2CO3 and/or NH4CO3 may be from about 1:1.5 to about 1.5:1, and particles may comprise MnCO3 with a tap density of from about 1.7 g/mL to 2.3 g/mL.
[0090] The volume of the reaction chamber, according to exemplary embodiments, may be about 300 mL or greater.
[0091] The residence time in the reaction chamber may be from about 1 second to about 60 minutes, may be from about 5 seconds to about 30 minutes, or may be from about 10 seconds to about 5 minutes.
[0092] A reactor for continuous generation of particles can have a reaction chamber with at least one entry, a source of ultrasonic irradiation (also referred to as a sonicator) for providing the ultrasonic irradiation to the reaction chamber, and at least one outlet port for removing the reaction overflow. In reactors with one entry port, the reaction solutions (for example, the MnSO4 solution and the NH4HCO3 solution) can be pre-mixed before being injected into the reaction chamber. In reactors with two entry ports, one of the entry ports can be for one of the reaction solutions (e.g. the MnSO4 solution) and another entry port can be for the other reaction solution (e.g. the NH4HCO3 solution). An embodiment of a reactor with two entry ports is illustrated in Figure 6, which shows reactor 100, reaction chamber 102, reagent entry ports 104 and 106, probe sonicator 108

-14-having probe tip 110, and an outlet port 112 for removing the reaction overflow (which, in a reaction between MnSO4 and NH4HCO3i would contain the generated MnCO3 particles).
The entry port(s) could be spaced between 1 mm and 50 cm away from themselves and/or from the source of the ultrasonic irradiation, or much greater (e.g. 1 m) depending on the power and intensity of the source of the ultrasonic irradiation and the size of the reaction chamber.
[0093] The source of ultrasonic irradiation can be, for example, a parallel transducer or a probe sonicator. One example of a probe sonicator is a Branson SonifierTM
450A (Branson Ultrasonics of Danbury CT, USA) that can operate at 400 W (10-100%
amplitude variation) and 20 kHz. Sonicators, operating at other frequencies (such as frequencies between 20 and 80 kHz), and operating at up to 100 kW, could alternatively be used. A probe sonicator can have a flat probe tip between 1 mm and 10 cm in diameter, or larger depending on the power and intensity of the source of the ultrasonic irradiation.
In particular embodiments, the probe tip can be 1.2 cm in diameter (having a surface area of 1.13 cm2). The probe tip can be vibrated with an amplitude of between 10 [tm and 5 cm.
In particular embodiments, the probe tip can be vibrated with an amplitude of about 150 gm. At maximum power, a Branson Sonifier 450A probe sonicator can have an intensity of about 350 W/cm2 using a probe tip with a diameter of 1.2 cm. Sonicators operating at an intensity of up to about 2000 W/cm2 can alternatively be used. The probe tip can be made of a variety of materials and can have a variety of textures.
[0094] Sonicators operated in air have a power output approaching zero since the viscosity of air is low. As the viscosity of the medium increases, the sonicator uses more power to vibrate. Sonifiers may show the actual power required to operate on the machine.
For the Branson Sonifier 450A operated in an aqueous medium with a 1.2 cm diameter flat probe tip, the power output is about 30% of 400 W (that is 120 W) at 100%
amplitude; and about 24% of 400W (that is 96 W) at 80% amplitude.
[0095] One or both of the two entry ports 104 and 106 can be positioned, as illustrated in Figure 6, to direct the reagent solutions near the probe tip, where sonication is more intense. A reactor can additionally include an outer jacket (not shown) which can be used to heat or cool the reaction chamber to a desired temperature.
[0096] Instead of probe sonicators, other reactors may use vibrating diaphragms or ultrasonic transducers attached to the reaction chamber walls to provide the ultrasonic

-15-irradiation. The reactor may include entry ports positioned to direct the reagent solutions into the reactor to quickly mix the reagents.
[0097] MnCO3 particles generated using a reactor having one entry port positioned to direct one of the two reagent solutions towards the probe head and the other entry port positioned to direct the second of the two reagent solutions away from the probe head, are illustrated in Figure 7. To produce the particles illustrated in Figure 7, 1 M
solutions of MnSO4 and NH4HCO3 were injected at 5 mL/min and mixed in a 50 mL continuous reactor at about 40 C and operating an 80% of full amplitude (or about 1.9 W/mL). The produced particles have a tap density of 1.48 g/mL (or about 40% of the crystal bulk density).
[0098] MnCO3 particles generated using a reactor with two entry ports positioned to direct the two reagent solution towards the probe head are illustrated in Figure 8, with the reaction conditions being the same as those used to produce the particles illustrated in Figure 7. The produced particles have a tap density of 1.59 g/mL (or about 43%
of the crystal bulk density).
[0099] A reactor used to produce the transition metal compound particles can accept reagents at different flow rates and reagents at different concentrations; the reactor can maintain the reaction at varying temperatures and/or pressures. In reactors that use probes to generate the ultrasonic irradiation, the reactor can provide ultrasonic irradiation at varying probe intensities and frequencies using probe tips of varying sizes and positioned in a variety of different locations. The reaction chamber can vary in size and geometry, and can be fabricated of different materials, thereby providing different surface textures of the reaction chamber. The reaction chamber can be actively stirred, for example using a stir bar, or can be mixed simply by the injection of the reagents.
[00100] In reactors that use probes to generate the ultrasonic irradiation, the aperture size just below the probe tip can be changed. Copper chips, steel shavings or plastic mesh, for example, can be added to the reaction chamber to increase surface area.
Gas, such as nitrogen, air or carbon dioxide, can be bubbled through the reaction chamber.
Surfactants, such as TweenTM-80 or mineral oil, and/or chelating agentscan be added to the reaction solution. For example, the surfactants and/or chelating agents can be added to one of the reagents or fed directly to into the reaction chamber.

-16-[001011 Chelating agents are agents which "coordinate" with the metal ion during particle growth and which may provide a mechanism for controlling particle size.
Examples of chelating agents which may be added to the reaction include, for example:
ammonium sulfate, ammonium hydroxide, ammonium chloride, ammonium acetate, ammonium nitrate, urea, or any combination thereof.
[001021 In particular embodiments of the reactor, the reagent entry ports are made from stainless steel tubing. The tubing can be movably adjustable so that the location of the reagent entry ports relative to the probe tip can be changed. In some embodiments, the reaction chamber can have a volume of between 2 mL and 1 L. Still larger sizes of reaction chambers are contemplated, for example reaction chambers having volumes of 25 L or larger, so long as the increased size of the chamber is offset by an increased sonication power and the ultrasonic irradiation intensity remains between about 0.1 W/mL
and 50 W/mL.
[001031 In particular embodiments, the reagent flow rates can be independently set to be between 1 mL/min and 1 L/min, or higher depending on the size of the reaction chamber. The reagent flow rates and reactor chamber can be chosen so that the residence time of the reagents and produced transition metal compound particles in the reaction chamber is greater than 5 seconds (where residence time is calculated as:
volume of reaction chamber divided by total flow rate of reagents). In particular embodiments, the residence time is 30 seconds or longer. In some embodiments, the resident time of the reagents can be 5 minutes or longer. In some embodiments, the reagent entry ports direct the reagents into a reaction volume where ultrasonic irradiation is provided at an intensity between about 0.1 W/mL and 50 W/mL thereby allowing the reagents to react before they move away from the ultrasonic irradiation. In one example, the reagent entry ports direct the reagents near the source of the ultrasonic irradiation, for example near a probe tip.
[001041 In particular embodiments, the ultrasonic irradiation provided by the probe can be between 10 and 100% of the maximum amplitude of the probe tip. The maximum amplitude of a probe tip being vibrated by a Branson Sonifier 450A is about 150 microns.
Alternative probe tips can be vibrated by other sonifiers to larger amplitudes.
Alternatively, other ultrasonic irradiation systems, such as diaphragm plate sonifiers, can be vibrated to larger amplitudes. In particular embodiments, the temperature of the reactor

-17-can be maintained using a heating or cooling jacket at a temperature between -20 C and 100 C.
[00105] In one particular reaction, 1 M MnSO4 and 1 M NH4HCO3 solutions were injected into a 50 mL reaction chamber at 5 mL/min, and subjected to 80% of full amplitude of ultrasonic irradiation (or about 1.9 W/mL). The ambient temperature of the reaction was maintained in an ice bath at 0 C. The resulting manganese carbonate particles produced are shown in Figure 9 and Figure 10. These particles have a tap density of 1.40 g/mL (or about 38% of the crystal bulk density).
[00106] In another reaction, 1 M MnSO4 and 1 M NH4HCO3 solutions were injected into a 50 mL reaction chamber at 5 mL/min, and subjected to 80% of full amplitude of ultrasonic irradiation (or about 1.9 W/mL). The ambient temperature of the reaction was maintained at 90 T. The resulting manganese carbonate particles produced are shown in Figure 11 and Figure 12. These particles have a tap density of 1.71 g/mL (or about 46% of the crystal bulk density).
[00107] Reactors having reaction chambers of different sizes can produce particles having different physical properties. For example, Figure 13, Figure 14 and Figure 15 (all shown at the same scale) show manganese carbonate particles produced using reaction chambers of 3 mL, 50 mL and 500 mL, respectively, using similar reaction conditions as described above with respect to the formation of the particles illustrated in Figures 9-12.
At 80% amplitude, the reactions were run at about 32 W/mL, about 1.9 W/mL and 0.19 W/mL, respectively. The produced particles have varied sizes and size distributions, as shown, with the particles illustrated in Figure 14 having nicely shaped spherical particles with a large size distribution and the particles illustrated in Figure 15 having irregularly shaped particles with a narrow size distribution.
[00108] Nickel manganese cobalt carbonate particles, where the nickel manganese cobalt source can include nickel, manganese and cobalt in any molar ratio, can be formed through the reaction between a nickel manganese cobalt source and a source of carbonate.
For example, the nickel manganese cobalt carbonate particles can be (Nili3Mnii3Coli3)C03 particles, which can be formed through the reaction between a transition metal salt providing a nickel manganese cobalt source, for example 1/3 NiSO4, 1/3 MnSO4 and 1/3 CoSO4 (written in shorthand notation as (Nili3Mni,3Coii3)S04 or NMC sulfate) or 1/3 Ni(N03)2, 1/3 Mn(N03)2 and 1/3 Co(N03)2 (similarly written in shorthand notation as

-18-(Niti3Mn1i3Coli3)(N03)2), and a source of carbonate, for example ammonium bicarbonate (NH4HCO3). In the above chemical formulas for the transition metal salt, the transition metal component TM corresponds to Nili3Mn113Co113 and the counter ion S of the salt corresponds to SO4 or (NO3)2, respectively. In other embodiments, the nickel manganese cobalt source can be, in shorthand notation: (Ni1i3Mn1i3Co1i3)(CH3000)2, or (Niti3Mn1i3Coti3)C12i and the carbonate source can be, for example, (NH4)2CO3, NaHCO3, Na2CO3, KHCO3, or K2C03.
[00109] In one particular embodiment, 0.2 M NMC sulfate and 1 M NH4HCO3 solutions were injected into a 50 mL reactor at 5 mL/min and subjected to ultrasonic irradiation at 80% of full amplitude (or about 1.9 W/mL). The resulting NMC
carbonate particles are shown in Figure 16.
[00110] In another embodiment, 0.2 M NMC sulfate and 2 M NH4HCO3 solutions were cooled to 3 C before being injected into a 50 mL reactor heated to 70 C
at 5 mL/min and subjected to ultrasonic irradiation at 80% of full amplitude (or about 1.9 W/mL). The resulting NMC carbonate particles (shown in Figure 17) have a tap density of 1.25 g/mL (or about 36% of the equimolar crystal bulk density).
[00111] After being collected, any produced particles can be dried, for example at 80 C for several hours.

Additional Embodiments for production of MnCO3 particles [00112] According to a further embodiment of the invention, exemplary particles can be formed using high intensity sonication within a large volume. The large volume can lead to larger particles and advantageously lead to a narrow size distribution in the particles formed and the high intensity (high W/mL) can lead to spherical or quasi-spherical particles. By using reagents in roughly equivalent concentrations, the impact of having a large excess of one reactant can be avoided. Particles having a narrow size distribution would be understood to be particles that have size distribution of at least 90%
of particles having a diameter within 25 m from the mean diameter. In some embodiments, the particles would have at least 90% of particles having a diameter within 15 m from the mean diameter. In other embodiments, the particles would have at least 90% of particles having a diameter within 10 m from the mean diameter. In yet other embodiments, the particles would have at least 90% of particles having a diameter within

-19-pm from the mean diameter. In some embodiments, the particles have a size distribution where at least 90% of particles are within 1 m and 50 pm. In other examples, at least 90% of the particles are within 1 pm and 30 pm. In yet other examples, at least 90% of the particles are within 3 gm and 20 pm. In still further examples, at least 90%
of the particles are within 3 m and 10 pm.
[00113] While spherical particles have advantages for downstream use, quasi-spherical or irregularly shaped particles that are not quite spherical are also desirable, if the size distribution is narrow, and the tap density is relatively high.
[00114] A reaction chamber volume greater than 300 mL can be considered a large volume. A reaction chamber volume from 350 mL to 700 mL can be used to advantageously result in a narrow size distribution of particles, while permitting a high throughput. Volumes in excess of 700 mL may be used, such as 1 L, 5 L, 10 L
and 25 L
volumes, for example, provided the sonication equipment is adequate to provide an ultrasonic irradiation having an intensity between about 0.1 W/mL and 50 W/mL
in the reaction volume and the flow rates are adequate to permit a suitable residence time.
[00115] In one particular test arrangement, a reaction chamber of 350 mL was used, with an indwelling sonicator adjacent to the reagent inputs. In one instance it was discovered that the filtrate had excess reagent - excess NH4HCO3 resulted in undesirable precipitation after adding MnSO4 to the filtrate. Further, excess MnSO4 was found to result in precipitation upon adding NH4HCO3, which is also undesirable.
[00116] The reaction of MnSO4 with NH4HCO3 forms the desired product MnCO3 as well as (NH4)2SO4, together with CO2 and H2O. The reaction of MnSO4 with Na2CO3 forms the desired product MnCO3 as well as Na2SO4. Figure 18 is a schematic representation of the precipitation that can occur when one of the reagents is present in significant excess. Within the left hand reaction chamber (1802), NH4HCO3 and/or Na2CO3 (1804) occurs in excess. In this case, precipitation within the "NH4HCO3 and/or Na2CO3 sea" of the reaction chamber occurs near the MnSO4 inlet (1806). Within the right hand reaction chamber (1812), MnSO4 (1814) occurs in excess. In this case, precipitation within the "MnSO4 sea" of the reaction chamber occurs near the NH4HCO3 and/or Na2CO3 inlet (1816). The sonicator, shown here in both instances as comprising a probe (1808 and 1818), can alternatively comprise another type of sonication device such as a diaphragm system or any number of ultrasonic transducers attached to the reaction

-20-chamber. This local precipitation near the inlets is undesirable. In these instances where excess reagent is present, precipitation occurs quickly upon entering the reaction chamber, which means that precipitation occurs at a relatively high concentration and in the presence of only a few particles. This leads to a wide distribution in particle sizes. It is desirable to attain a narrow size distribution. Thus, by avoiding excesses of reagent, the likelihood of producing particles with a wide size distribution is diminished.
[00117] Figure 19 is a schematic representation of the reaction when neither reactant is present in excess. Within the reaction chamber (1902), NH4HCO3 and/or Na2CO3 (1904) and MnSO4 (1906) are provided to form the desired MnCO3 particles, as well as (NH4)2SO4 and/or Na2SO4, or a mixture of these products in solution.
Here, neither incoming reagent sees a "sea" of the other, so reagents are allowed to mix more intimately before precipitation occurs. This leads to more uniform particle growth, possibly because precipitation occurs at lower concentration and around many more particles. It may be advantageous to locate input ports for the two reagents relatively far away from each other in the chamber, to allow intimate mixing before precipitation occurs.
[00118] Using Na2CO3 was found to yield good tap density and good uniformity of particles (narrow size distribution). A good tap density of 1.6 to 2.2 g/mL
can be achieved, and a tap density of about 2.1 g/mL was observed when using Na2CO3 with MnSO4, in amounts such that that neither reagent was in excess. The reaction was conducted at 70 C
producing relatively uniform, quasi-spherical particles.
[00119] In one instance, 2 M NH4HCO3, was used with 1 M MnSO4 in a 50 mL
reaction chamber subjected to ultrasonic irradiation at 80% of full amplitude (about 1.9 W/mL). Excess NH4HCO3 was observed. A wide size distribution was observed. The tap density observed was 1.85 g/mL. The upper portion of Figure 20 provides an SEM
micrograph showing the resulting MnCO3 particles with a wide size distribution. By way of comparison, in another instance, 0.6 M NH4HCO3 was used with 0.5 M MnSO4 in a 300 mL reaction chamber subjected to ultrasonic irradiation at 80% of full amplitude (about 0.32 W/mL). No excess was observed, and a narrow size distribution was achieved.
The tap density in this instance was 1.70 g/mL. The lower portion of Figure 20 provides a SEM micrograph showing the resulting MnCO3 particles with a narrow size distribution.
These instances illustrate that it is undesirable to provide reagents in excess because of the resulting wide size distribution.

-21-[00120] In another instance, 0.6 M NH4HCO3 and 0.5 M MnSO4 were used in a reaction that started with water. In this case, reagents were used in roughly equivalent amounts, and no excess was observed. The resulting particles had a narrow size distribution and a tap density of 1.70 g/mL. By way of contrast, instead of starting with water, the reaction started with 0.5 M (NH4)2SO4 (a by-product of the reaction). In this instance, although no excess was observed, a wide size distribution was observed and the tap density was 1.87 g/mL. For both experiments, a 300 mL reaction chamber was used and was subjected to ultrasonic irradiation at 80% of full amplitude (about 0.32 W/mL).
This example suggests a high amount of (NH4)2SO4 is also undesirable in achieving a narrow size distribution.

[00121] In a further instance, a tap density of 2.05 g/mL for MnCO3 was achieved with a desirable narrow size distribution. In this instance, 1 M MnSO4 was used with 1.08 M Na2CO3. The 700 mL reaction chamber was subjected to ultrasonic irradiation at 100%
amplitude (about 0.17 W/mL). The conditions of this example included 80 %
amplitude of the sonicator and flow rates of 5 mUmin for each reactant. The reaction proceeded at 65 C, with no pH control. In this instance, MnCO3 particles were achieved with the highly desirable tap density, a decent particle size, and a narrow size distribution.
Figure 21 illustrates the particles obtained in this instance. An SEM micrograph showing the resulting MnCO3 particles at a lower magnification (left) as well as a higher magnification (right) is provided to indicate good particle size and narrow size distribution.
[00122] Advantageously, the production of particles is fast and efficient due to a residence time in the reaction chamber on the order of a few minutes. The production of particles can be conducted using very high reactant concentrations of 1 to 2 M. Further, no pH monitoring is required in the method described, nor are other additional chemicals such as surfactants required. The high yield produced in this instance is fast and results in less waste, potentially increasing efficiencies and reducing cost.
[00123] Particles with a narrow size distribution can be obtained using the arrangement and method described. For a small reaction chamber, small particles and a wide size distribution may result, possibly due to inadequate mixing of reagents before reacting. Thus, by increasing the volume to be greater than 300 mL, which can scale up to 700 mL or volumes greater than 25 L with appropriate equipment, intimate mixing within

-22-the reaction chamber is possible, producing particles that are larger and more uniform in size.
[00124] In additional examples and conditions tested, it was found that by varying the amplitude of the probe from 0% to 100% in 20% increments in a reaction of MnSO4 and 1 M NH4HCO3 (at a flow rate of 5 mL/min), the tap density increases steadily.
In general, high amplitudes (or high sonication intensity (high W/mL)), lead to more spherical particles. Particles move more from irregular shapes to quasi-spherical and spherical shapes at about the 50% amplitude range (about 60 W output power in an aqueous medium using Branson SonifierTM 450A with flat probe tip of diameter 1.2 cm), which corresponds to about 1.2 W/mL when using a continuous reactor volume of about 50 mL.
[00125] When flow rates are adjusted using the same reactants at 100%
amplitude in a 700 mL continuous reactor, flow rates of 10 mL/min and below give desirable tap densities. Larger flow rates are preferred for higher throughput. Larger flow rates may be used with larger reaction volumes (with appropriate sonication power).
[00126] Particles according to the present disclosure may be obtained by flowing, for example, approximately 1 M MnSO4 and approximately 1 M Na2CO3 each at a flow rate of, for example, 50 mL/min, into a well mixed reaction chamber of volume, for example, 1 L. A chelating agent, such as 0.1 M (NH4)2SO4 may be added with the MnSO4. Ultrasonic irradiation is delivered to the contents of the reaction volume such that the irradiation is substantially uniform throughout the volume and the power density that is delivered is greater than, for example, 1 W/mL. In some examples, the power density may be approximately 3 W/mL. The ultrasonic source may be two or more ultrasonic transducers attached to the external surface of the reaction chamber so that the source of irradiation is spread over the ends of a cylindrical reaction chamber or over the entire surface of the reaction chamber. Preferably, the two inlet ports may be spaced as far apart as the reaction chamber will allow, placing the outlet port so that it is substantially equidistant from both inlet ports.
[00127] In reaction chambers that use a localized source (non-uniform) of ultrasonic irradiation, such as an ultrasonic probe tip it may be desirable to space the two inlet ports as far apart as the reaction chamber will allow, placing the outlet port so that it is equidistant from both inlet ports.

-23-[00128] For a narrow size distribution, separating the reagent entry ports is desirable. Separating the reagent entry ports allows the reagents to be diluted and well mixed with the contents of the reaction chamber before precipitation occurs.
Production Of MHC03 particles [00129] Figure 22 shows MnCO3 particles produced in a 700 mL continuous reactor at 70 C under stirring using 1 M MnSO4 and 1.5 M Na2CO3 each fed at 5 mL/min.
The produced particles have a tap density of 1.47 g/mL (or about 40% of the crystal bulk density).
[00130] Figure 23 shows MnCO3 particles produced in a 700 mL continuous reactor at 70 C under sonication (Branson 450A; 20 kHz, 400 W, 10% - 100%
amplitude control) at 100% amplitude (about 0.17 W/mL) by the reaction of 1 M MnSO4 and 1.5 M
Na2CO3 each fed at 5 mL/min. The produced particles have a tap density of 1.65 g/mL (or about 45% of the crystal bulk density). No sonication during the reaction results in large agglomerated particles (as illustrated in Figure 22), while sonication during the reaction results in smaller, less agglomerated particles (Figure 23).
[00131] Figure 24 shows MnCO3 particles generated using a continuous reactor under the same conditions as that of Figure 7, except that the temperature of the reactor was 70 C and the reactor had two entry ports positioned to direct the two reagent solution towards the probe head. The produced particles have a tap density of 1.79 g/mL
(or about 48% of the crystal bulk density).
[00132] Figure 25 shows MnCO3 particles generated using the same conditions as that of Figure 24, except Na2CO3 was used instead of NH4HCO3. The produced particles have a tap density of 1.74 g/mL (or about 47% of the crystal bulk density).
[00133] Figure 26 shows MnCO3 particles produced in a 700 mL continuous reactor at 70 C under sonication at 100% amplitude (or about 0.17 W/mL) when feeding 1 M Na2CO3 and 1.5 M MnSO4 at 5 mL/min. The resulting particles have a tap density of 1.73 g/mL. A wide size distribution was observed.
[00134] By way of comparison, Figure 27 shows MnCO3 particles produced when 1.05 M Na2CO3 was used with 1 M MnSO4 under the same conditions as the particles seen in Figure 26. The resulting particles have a tap density of 1.94 g/mL. No excess was observed, and a narrower size distribution of larger particles was achieved.

-24-[00135] Figure 28 shows MnCO3 particles produced when 0.7 M NH4HCO3 and 0.5 M MnSO4 were each added at 5 mL/min to a 300 mL continuous reactor kept at that was initially charged with 0.5 M (NH4)2SO4 (a by-product of the reaction) (instead of distilled water), and where the reagents were reacted under sonication at 80%
amplitude (or about 0.32 W/mL). The resulting particles have a tap density of 1.87 g/mL.
Although no excess was observed, a wide size distribution was observed. This example suggests that a high amount of (NH4)2SO4 is undesirable in achieving a narrow size distribution.
However, the MnCO3 particles were relatively large. This suggests that a high amount of (NH4)2SO4 is desirable in obtaining large particles and, further, that varying amounts of (NH4)2SO4 could allow for particle size control.
[00136] Figure 29 shows MnCO3 particles produced when a mixture of 1 M
MnSO4 with 0.05 M (NH4)2SO4 was added with 1.05 M Na2CO3, each at 5 mL/min, to a 700 mL continuous reactor kept at 70 C and reacted under sonication at 100%
amplitude (or about 0.17 W/mL). The resulting particles have a tap density of 2.02 g/mL.
[00137] Figure 30 shows MnCO3 particles produced when a mixture of 1 M
MnSO4 with 0.03 M (NH4)2SO4 was added with 1.08 M Na2CO3, each at 5 mL/min, to a 700 mL continuous reactor kept at 70 C and reacted under sonication at 100%
amplitude (or about 0.17 W/mL). The resulting particles have a tap density of 2.11 g/mL.
The particles illustrated in Figures 30 and 31 suggest that a small amount of (NH4)2SO4 is desirable in achieving relatively large particles with a more uniform size distribution.
[00138] Figure 31 illustrates particle size distribution plots for samples shown within the present application. Panel A illustrates the particle size distribution of the sample shown in Figure 22, panel B illustrates the particle size distribution of the sample shown in Figure 23, panel C illustrates the particle size distribution of the sample shown in Figure 7, panel D illustrates the particle size distribution of the sample shown in Figure 24, panel E illustrates the particle size distribution of the sample shown in Figure 25, panel F
illustrates the particle size distribution of the sample shown in Figure 17, panel G
illustrates the particle size distribution of the sample shown in Figure 26, panel H
illustrates the particle size distribution of the sample shown in Figure 27, panel I illustrates the particle size distribution of the sample shown in Figure 28, panel J
illustrates the particle size distribution of the sample shown in Figure 29, and panel K
illustrates the particle size distribution of the sample shown in Figure 30.

-25-[00139] In the preceding description, for purposes of explanation, numerous details are set forth in order to provide a thorough understanding of the embodiments.
However, it will be apparent to one skilled in the art that these specific details are not required.
[00140] The above-described embodiments are intended to be examples only.
Alterations, modifications and variations can be effected to the particular embodiments by those of skill in the art without departing from the scope, which is defined solely by the claims appended hereto.

-26-

Claims (22)

CLAIMS:

1. A method of preparing insoluble transition metal compound particles in a reaction chamber, said particles represented by the formula (TM)(S'), the method comprising:
providing a transition metal salt solution, the transition metal salt having the formula (TM)(S) and comprising transition metal component (TM) is one or more transition metal independently selected from the group consisting of Mn, Ni, Co, Mg, Zn, Ca, Sr, Cu, Zr, P, Fe, Al, Ga, In, Cr, Ge and Sn;
providing source of an anionic compound, the anionic compound being a carbonate-, hydroxide-, phosphate-, oxyhydroxide- or oxide-based compound, said anionic compound comprising an anionic component represented by S', wherein said anionic component is reactive with the transition metal component TM to form the insoluble transition metal compound particles;
adding the transition metal salt solution and the anionic compound to a reaction chamber; and subjecting the reaction chamber to sonication at an intensity of from about 0.1 to about 50 W/mL to form the insoluble transition metal compound particles.

2. The method according to claim 1, wherein the intensity is from about 1 W/mL
to about 5 W/mL.

3. The method according to claim 1, wherein the intensity is about 3 W/mL.

4. The method according to any one of claims 1 to 3, wherein the transition metal salt solution comprises MnSO4, Mn(CH3COO)2, MnCl2, or Mn(NO3)2.

5. The method according to any one of claims 1 to 4, wherein the source of the anionic compound is a solution comprising Na2CO3, NH4HCO3, (NH4)2CO3, NH4OH, NaHCO3, NaOH, KHCO3, K2CO3, KOH, H3PO4, NaH2PO4, Na2HPO4, (NH4)3P04, (NH4)2HPO4, (NH4)H2PO4, (NH4)2NaPO4, (NH4)Na2PO4, KH2PO4, K2HPO4, (NH4)2KPO4, (NH4)K2PO4, or KMnO4.

6. The method according to claim 5, wherein the source of the anionic compound is a solution comprising Na2CO3 and/or NH4HCO3.

7. The method according to any one of claims 1 to 6, wherein the ratio of the anionic compound to the transition metal salt in the reaction chamber is from about 1:1.5 to about 1.5:1.

8. The method according to claim 7, wherein the ratio of the anionic compound to the transition metal salt in the reaction chamber is about 1:1.

9. The method according to any one of claims 1 to 7, wherein sonication is provided by a probe tip, by vibrating diaphragms, or by any number of ultrasonic transducers attached to reaction chamber walls.

10. The method according to any one of claims 1 to 9, wherein the reaction chamber comprises a flow-through chamber.

11. The method according to any one of claims 1 to 10, wherein the insoluble transition metal compound particles are spherical, quasi-spherical or irregular in shape.

12. The method according to any one of claims 1 to 11, wherein the insoluble transition metal compound particles produced have a particle size distribution of at least 90% of particles within 1 µm and 50 µm; at least 90% within 1 µm and 30 µm; at least 90% within 3 µm and 20 µm; or at least 90% within 3 µm and 10 µm.

13. The method according to any one of claims 1 to 12, wherein the insoluble transition metal compound particles produced comprise MnCO3 having a tap density from about 1.5 g/mL to about 3.0 g/mL.

14. The method according to any one of claims 1 to 13, wherein the insoluble transition metal compound particles produced have a tap density from about 1.7 g/mL to about 2.3 g/mL.

15. The method according to claim 1, wherein the transition metal salt solution comprises MnSO4, the source of the anionic compound is a solution comprising Na2CO3 and/or NH4HCO3, the ratio of MnSO4 to Na2CO3 and/or NH4HCO3 is from about 1:1.5 to about 1.5:1, and particles comprise MnCO3 with a tap density of from about 1.7 g/mL to 2.3 g/mL.

16. The method according to any one of claims 1 to 15, wherein the volume of the reaction chamber is 300 mL or greater.

17. The method according claim 16, wherein the transition metal salt solution and the anionic compound are added to a reaction chamber via reagent entry ports positioned more than about 10 cm apart from each other.

18. The method according to any one of claims 1 to 17, wherein the residence time in the reaction chamber is from about 1 second to about 60 minutes, or is from about 5 seconds to about 30 minutes, or is from about 10 seconds to about 5 minutes.

19. The method according to any one of claims 1 to 18, further comprising adding a chelating agent to the reaction chamber.

20. The method according to claim 19, wherein the chelating agent is ammonium sulfate, ammonium hydroxide, ammonium chloride, ammonium acetate, ammonium nitrate, urea, or any mixture thereof.

21. The method according to any one of claims 1 to 20, wherein the reaction chamber is at a temperature of from about -20 °C to about 100 °C, from about 0°C to about 100 °C, from about 30 °C to about 100 °C, or from about 50 °C to about 100 °C.

22. The method according to any one of claims 1 to 21, wherein:
the transition metal salt solution is at a concentration from about 0.1 M to about 5 M, about 0.5 M to about 3 M, or about 1 M to about 2 M; and the anionic compound solution is at a concentration from about 0.1 M to about M, about 0.5 M to about 3 M, or about 1 M to about 2 M.