US20150353374A1

US20150353374A1 - Rutile titanium dioxide microspheres and ordered botryoidal shapes of same

Info

Publication number: US20150353374A1
Application number: US14/827,406
Authority: US
Inventors: Guoyi Fu; Mark B. Watson
Original assignee: CRISTAL INORGANIC CHEMICALS SWITZERLAND Ltd
Current assignee: CRISTAL INORGANIC CHEMICALS SWITZERLAND Ltd
Priority date: 2013-03-15
Filing date: 2015-08-17
Publication date: 2015-12-10
Also published as: WO2014140840A3; WO2014140840A2; US20140272416A1; US9108862B2

Abstract

Rutile TiO₂microspheres and microparticles in a botryoidal morphology which form from ordered acicular aggregates of elongated TiO₂crystallites that resemble nano-sized flower bouquets and/or triangular funnels, and process for their preparation by thermally hydrolyzing a soluble TiO₂precursor compound in aqueous solution in the presence of a morphology controlling agent selected from carboxylic acids and amino acids.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS/INCORPORATION BY REFERENCE STATEMENT

The present application is a Divisional of U.S. application Ser. No. 13/842,608, filed Mar. 15, 2013. The entirety of which is hereby expressly incorporated herein by reference.

BACKGROUND OF THE INVENTION

The presently described and claimed inventive concept(s) relates to a novel chemical structure comprising rutile titanium dioxide (TiO₂) microspheres which are formed by aggregation of funnel-shaped rutile nanoparticles in which the broader dimension of the funnels assemble during hydrolysis to become the outer surface of the microspheres. More particularly, ordered aggregates of such microspheres further aggregate to resemble a larger botryoidal morphology.
Titanium dioxide (TiO₂) is known as a typical solid compound having photocatalytic activity and having utility in electronic, photovoltaic and photonic applications. Rutile and anatase crystal forms are known as major crystal forms of TiO₂which display higher chemical stability and larger refractive indices than those of amorphous TiO₂. It has also been recognized that TiO₂particles having a high degree of crystallinity can exhibit a desirable level of photocatalytic activity.
U.S. Patent Publication No. 2012/0132515, for example, describes rutile TiO₂nanoparticles wherein each has an exposed crystal face, making the nanoparticles useful as a photocatalyst and oxidation catalyst. The TiO₂nanoparticles are produced by subjecting a titanium compound to a hydrothermal treatment in an aqueous medium in the presence of a hydrophilic polymer, which is polyvinylpyrrolidone. The titanium compound, when hydrothermally treated in an aqueous medium, generally gives a rod-like crystal of rutile titanium dioxide having (110) and (111) faces. However, when hydrothermally treated in an aqueous medium in the presence of polyvinylpyrrolidone, the rod-like crystal which results exhibits a novel exposed crystal face (001). It is noted that the hydrophilic polymer acts as a steric stabilizer or capping agent to thereby prevent aggregation of the rod-like crystals of rutile titanium dioxide.
The need exists for improved methods for producing novel types of rutile titanium dioxide (TiO₂) nano- and microparticles which have high surface areas, e.g., in the range of from 120 m²/g to 160 m²/g, and high refractive indices for improved UV blocking capability and which demonstrate high performance levels in catalysis, e.g., biomass conversion, and in electronic applications, such as lithium ion batteries and fuel cells.

SUMMARY OF THE INVENTION

The described and claimed inventive concepts(s) comprise, in one embodiment, a method for preparing a novel form of rutile TiO₂nanoparticles which are ordered acicular aggregates of elongated TiO₂crystallites. The elongated TiO₂crystallites are rod-like, e.g., slender and/or needle-like, having a thickness of from 3 nm to 5 nm and a length which can vary from 20 nm up to 50 nm, although longer and shorter lengths may also be present. However, the elongated TiO₂crystallites assemble together during the process in a manner which results in ordered acicular aggregates that resemble nano-sized flower bouquets or triangular funnels. By controlling the hydrolysis conditions according to the inventive concept(s) described herein, the nano-sized flower bouquets or triangular funnel-shaped nanoparticles further aggregate into somewhat larger spherical structures, i.e., microspheres, having a diameter of from 1 to 2 microns. The particles aggregate in such a manner that the broader ends of the funnel-shaped particles become the outer surfaces of the microspheres where the tips of the funnels join, i.e., become assembled together, at the center of the microspheres.
The method for preparing the microspheres comprises:
(a) forming an aqueous solution of a soluble titanium compound at a titanium concentration of from 0.5 to 1.0 moles per liter;
(b) introducing a morphology controlling agent selected from an α-hydroxy carboxylic acid of the formula R—CH(OH)COOH, an α-hydroxy carboxamide of the formula R—CH(OH)CONH₂or an α-amino acid of the formula R—CH(NH₂)COOH, wherein R is an alkane, alkene, alkyne, arene, or cycloalkane group having 4 or fewer carbon atoms, into the solution at an acid- or carboxamide-to-titanium molar ratio of from 0.02 to 0.2 while simultaneously heating the solution to a temperature in the range of from 75° C. to 80° C. with constant stirring;
(c) maintaining the stirred solution at a temperature in the range of from 75° C. to 80° C. for a period of from one to 3 hours;
(d) elevating the temperature of the stirred solution to a value of from 100° C. to the refluxing temperature and maintaining said temperature for a period of from 2 hours to 4 hours to form a reaction product;
(e) optionally neutralizing the reaction mixture which results from step (e);
(f) cooling the reaction mixture to room or ambient temperature; and
(h) separating and drying the reaction product.
The reaction product can then be calcined. Calcining, which can be adjusted over a wide range for time and temperature, operates to enhance the properties of the resulting nanoparticles by expanding or opening the pore structure and/or increasing the refractive index.
The morphology controlling agent is selected from lactic acid (CH₃CH(OH)COOH); 2-hydroxybutyric acid (C₂H₅CH(OH)COOH); 2-hydroxypentanoic acid (C₃H₇CH(OH)COOH); 2-Hydroxyhexanoic acid (C₄H₉CH(OH)COOH); 2-Hydroxyisocaproic acid (CH₃CH(CH₃)CH₂CH(OH)COOH); alanine (CH₃CH(NH₂)COOH); valine (CH₃CH(CH₃)CH(NH₂)COOH); norvaline (C₃H₇CH(NH₂)COOH); isoleucine (C₂H₅CH(CH₃)CH(NH₂)COOH); leucine (CH₃CH(CH₃)CH₂CH(NH₂)COOH); and norleucine (C₄H₉CH(NH₂)COOH) and mixtures thereof.
The soluble titanium compound is selected from titanium oxychloride (TiOCl₂), titanium oxybromide (TiOBr₂), titanium oxyiodide (TiOI₂), titanium oxynitrate (TiO(NO₃)₂), titanium trichloride (TiCl₃), titanium tribromide(TiBr₃), titanium oxalate (Ti₂(C₂O₄)₃), potassium hexafluorotitanate(K₂TiF₆), ammonium hexafluorotitanate ((NH₄)₂TiF₆), potassium titanyloxolate (K₂TiO(C₂O₄)₂), ammonium titanyloxolate ((NH₄)₂TiO(C₂O₄)₂), titanium bis(ammonium lactate) dihydroxide ([CH₃CH(O)COONH₄]₂Ti(OH)₂) and mixtures thereof.
According to another embodiment, the described and claimed inventive concept(s) relates to a method for preparing rutile TiO₂particles which comprise structures in a botryoidal morphology having a size in the range of from 10 to 20 microns. The botryoidal structures, also being aggregates of elongated TiO₂crystallites having a thickness of from 3 nm to 5 nm, are formed by introducing TiO₂seeds into the stirred solution at a seed-to-TiO₂molar ratio of from 0.0005 to 0.0015 following introduction of the morphology controlling agent. The stirred solution is then maintained at a temperature in the range of from 75° C. to 80° C. for a period of from one to 3 hours, and the process is further carried out as described above.
The described and claimed inventive concept(s) include, in other embodiments, the microspheres and the botryoidal particles produced by the described processes.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is an SEM (Scanning Electron Microscopy) image (9500 magnification) of spherical-shaped rutile TiO₂microparticles according to the invention.

FIG. 2 is an enlarged SEM image (50,000 magnification) which illustrates in more detail the spherical-shaped rutile TiO₂microparticles according to the invention.

FIG. 3 is an SEM image (10,000 magnification) which illustrates spherical- shaped rutile TiO₂microparticles arranged in structures which resemble a botryoidal morphology according to the invention.

FIG. 4 is an enlarged SEM image (50,000 magnification) which illustrates the botryoidal morphology according to the invention in more detail.

FIGS. 5 and 6 are SEM images of rutile TiO₂microparticles prepared by thermal hydrolydsis according to Example 3, but without benefit of a morphology controlling agent.

DETAILED DESCRIPTION OF THE INVENTION

The described and claimed inventive concepts(s) comprise, in one embodiment, a method for preparing a novel form of rutile TiO₂nanoparticles which are ordered acicular aggregates of elongated TiO₂crystallites. The elongated TiO₂crystallites are rod-like and have a thickness of from 3 nm to 5 nm and a length which can vary generally from 20 nm up to 50 nm. However, the elongated TiO₂crystallites assemble together during the process in a manner which results in ordered acicular aggregates that resemble nano-sized flower bouquets or triangular funnels. By controlling the hydrolysis conditions according to the inventive concept(s) described and claimed herein, the nano-sized flower bouquets or triangular funnel-shaped nanoparticles further aggregate into somewhat larger spherical structures, i.e., microspheres, having a diameter of from 1 to 2 microns. Detailed examination under an electron microscope confirms that the microspheres are indeed formed by aggregation of the funnel-shaped nanoparticles. The microspheres can be seen in FIGS. 1 and 2. The hydrolysis conditions are controlled in such a manner that the nanoparticles aggregate so that the broader ends of the funnel-shaped particles become the outer surfaces of the microspheres, and the tips of the funnels join, i.e., assemble together, at the center of the microspheres. The structure observed for the microspheres indicates a large number of rutile nano-rods with various lengths radiating outwardly from the center of the spherical structures with each of the rods aligning at an angle normal to the surface of the spheres.
The novel rutile TiO₂microspheres are prepared by thermally hydrolyzing a soluble TiO₂precursor compound, or a mixture of such compounds, in aqueous solution in the presence of a morphology controlling agent, or a mixture of morphology controlling agents, under specific conditions. The process is a wet chemical hydrolysis method in which the structure of the microspheres is controlled by controlling the structure of the nano-sized flower bouquets or triangular funnel-shaped nanoparticles. A morphology controlling agent, or a mixture of morphology controlling agents, is used that is selected from (i) an α-hydroxy carboxylic acid of the formula R—CH(OH)COOH, (ii) an α-hydroxy carboxamide of the formula R—CH(OH)CONH₂, or (iii) an α-amino acid of the formula R—CH(NH₂)COOH, wherein R is an alkane, alkene, alkyne, arene, or cycloalkane group having 4 or fewer carbon atoms.
The process begins by forming an aqueous solution of a soluble titanium compound at a titanium concentration of from 0.1 to 1.5 moles per liter, but preferably 0.5 to 1.0 moles per liter, optionally in the presence of a mineral acid. Distilled or deionized water can be used to form the aqueous solution, and a mineral acid, e.g., hydrochloric acid (HCl), can be introduced as needed for controlling the rate of hydrolysis.
The morphology controlling agent, or a mixture thereof, is introduced into the solution at an acid- or carboxamide-to-titanium molar ratio of from 0.02 to 0.4, although best results have been observed when the ratio is from 0.02 to 0.2. The solution is simultaneously heated to a temperature in the range of from 75° C. to 80° C. with constant stirring.
The temperature of the stirred solution is next elevated to a value of from 100° C. to the refluxing temperature and maintained at that level for a period of from 2 hours to 4 hours during which time a reaction product is formed. The solution, i.e., reaction mixture, is then cooled to room or ambient temperature, and, optionally, it can be neutralized, e.g., pH of 5 to 8, with introduction of a base, such as an ammonia solution or a sodium hydroxide solution. The reaction product is then separated by filtration and washed with dionized water to remove salts generated during hydrolysis. The resulting filter cake can then be dried in an oven or re-slurried with water and spray dried.
As noted above, the reaction product can then be calcined as desired over a wide range of time and temperature to enhance the properties of the resulting nanoparticles, such as by expanding or opening the pore structure and/or increasing the refractive index.
For best results the soluble titanium precursor compound is selected from titanium oxychloride (TiOCl₂), titanium oxybromide (TiOBr₂), titanium oxyiodide (TiOI₂), titanium oxynitrate (TiO(NO₃)₂), titanium trichloride (TiCl₃), titanium tribromide(TiBr₃), titanium oxalate (Ti₂(C₂O₄)₃), potassium hexafluorotitanate(K₂TiF₆), ammonium hexafluorotitanate ((NH₄)₂TiF₆), potassium titanyloxolate (K₂TiO(C₂O₄)₂), ammonium titanyloxolate ((NH₄)₂TiO(C₂O₄)₂), and titanium bis(ammonium lactate) dihydroxide ([CH₃CH(O)COONH₄]₂Ti(OH)₂). Other commercially available soluble titanium precursor compounds can be deployed in the process and produce satisfactory results and, although not specifically named herein, they are embraced within the described and claimed inventive concept(s).
As noted above, morphology controlling agents, or mixtures thereof, for carrying out the inventive concept(s) include (i) α-hydroxy carboxylic acids of the formula R—CH(OH)COOH, (ii) α-hydroxy carboxamides of the formula R-—CH(OH)CONH₂, and (iii) α-amino acids of the formula R—CH(NH₂)COOH, wherein R is an alkane, alkene, alkyne, arene, or cycloalkane group having 4 or fewer carbon atoms. Examples of such morphology controlling agents include, but are not limited to, lactic acid (CH₃CH(OH)COOH); 2-hydroxybutyric acid (C₂H₅CH(OH)COOH); 2-hydroxypentanoic acid (C₃H₇CH(OH)COOH); 2-Hydroxyhexanoic acid (C₄H₉CH(OH)COOH); 2-Hydroxyisocaproic acid (CH₃CH(CH₃)CH₂CH(OH)COOH); alanine (CH₃CH(NH₂)COOH); valine (CH₃CH(CH₃)CH(NH₂)COOH); norvaline (C₃H₇CH(NH₂)COOH); isoleucine (C₂H₅CH(CH₃)CH(NH₂)COOH); leucine (CH₃CH(CH₃)CH₂CH(NH₂)COOH); and norleucine (C₄H₉CH(NH₂)COOH) and mixtures thereof.
It has also been discovered according to the inventive concept(s) described herein that the hydrolysis conditions can be further adjusted to produce even larger aggregates of about 10 to 20 microns in size which exhibit a botryoidal morphology or texture. A botryoidal texture is one in which the particle has a globular external form resembling, for example, a bunch of grapes. The botryoidal structures, also being aggregates of the elongated TiO₂crystallites, form when TiO₂seeds are introduced into the stirred solution at a seed-to-TiO₂molar ratio of from 0.0005 to 0.0015 following introduction of the morphology controlling agent. The stirred solution is then maintained at a temperature in the range of from 75° C. to 80° C. for a period of from one to 3 hours, and the process is further carried out as described above. The rutile TiO₂microspheres and the botryoidal particles become denser and their pore volumes become lower in comparison with the funnel-shaped triangular nanoparticles, although the powder specific surface areas for the particle varieties are similar to one another, i.e., in the range from 120 m²/g to 160 m²/g. Typical pore volumes for the microspheres and botryoidal particles are in the range of from 0.1 cm³/g-0.3 cm³/g.

EXAMPLES

The present invention will be illustrated in further detail with reference to the working examples which follow and FIGS. 1-8. It should be noted, however, that these examples should not be construed to limit the scope of the described and claimed inventive concept(s).

Example 1

Preparation of TiO₂Microspheres Using Carboxylic Acids

1,255 g of deionized water, 6.6 g lactic acid (85% solution from Alfa Aesar), 97 g HCl solution (37% from Fisher Scientific), and 397 g of titanium oxychloride solution (25.2% in TiO₂, from Millennium Inorganic Chemicals) were mixed together in a heated reactor equipped with a glass condenser and an overhead stirrer. While being constantly stirred, the mixture was heated to 75° C., and the hydrolysis reaction was maintained at 75° C. for 2 hours. The reaction temperature was then increased to 103° C., and that temperature was maintained for 4 hours. The hydrolysis was essentially complete at this stage.
The resulting reaction mixture was then cooled to room temperature and transferred to a different container where the particles formed were allowed to settle for a few hours. After essentially all of the particles were observed to have settled to the bottom of the container, the mother liquor, i.e., liquid reaction medium, was removed and about the same volume of fresh deionized water was added to the container. The reaction mixture was then stirred to re-slurry the particles, and then the pH of the slurry was increased to a value of about 7 by slow addition of an ammonia solution (˜29%, Fisher Scientific). The particles comprising the reaction product were then separated from the liquid reaction mixture using a Buchner filter and washed with deionized water until the conductivity of the filtrate was lowered to about 500 μS/cm. The wet filter cake sample was then stored as a slurry by re-slurring the filter cake with a small amount of deionized water. The powder form of the sample was obtained by drying the slurry sample in an oven overnight at 90° C. X-ray Diffraction (XRD) measurement on the powder sample indicates that the sample contained 100% rutile with crystallite size about 7.6 nm. BET measurement on the powder sample showed that the powder had a specific surface area of 122 m²/g and a pore volume of 0.1 cm³/g.
SEM images of the slurry sample are shown in FIG. 1 at a magnification of 9,500 where the spherical microspheres can be observed. Enlarged microspheres can be seen more clearly in FIG. 2 at a magnification of 50,000.
The TiO₂microspheres shown in FIGS. 1 and 2 can be calcined, which can be adjusted for time and temperature, to enhance the properties of the resulting microparticles by expanding or opening the pore structure and/or increasing the refractive index.

Example 2

Preparation of Botryoidal Micro-Particles Using Carboxylic

The same procedure was followed as was followed in Example 1, except that 13.2 g of lactic acid (85% solution from Alfa Aesar) was added. In addition, the final hydrolysis temperature was maintained at 95° C. for 4 hours instead of 103° C. SEM images of the sample are shown in FIG. 3 at a magnification of 10,000. A botryoidal texture can be observed in which the particle has a globular external form resembling, for example, a bunch of grapes. FIG. 4 shows an enlarged SEM image (b 50,000 magnification) which illustrates the botryoidal morphology in more detail.
XRD measurement of the sample confirmed that the sample contained 100% rutile TiO₂with a crystallite size of 7.8 nm. BET measurement showed a specific area of 161 m²/g and a pore volume of 0.12 cm³/g.

Comparative Example 3

Hydrolysis without a Morphology Controlling Agent(s)

The same procedure was followed as was followed for Example 1, except that no organic acids (morphology controlling agent) were added during the procedure. SEM images of the sample can be seen in FIGS. 5 and 6. XRD measurement showed that the sample contained 100% rutile TiO₂, however, the SEM images show clearly that the sample prepared by thermal hydrolysis without a morphology controlling agent has a different morphology than the microsphere and botryoidal particle samples shown in FIGS. 1-4 in which a morphology controlling agent was used.

Claims

1-7. (canceled)

8. Rutile TiO₂microparticles which comprise generally spherical structures in the range of from 1 to 2 microns in diameter, said spherical structures comprising ordered acicular aggregates of elongated TiO₂crystallites having a thickness in the range of from 3 nm to 5 nm in which one end of each of said elongated TiO₂crystallites are joined into a cluster such that the opposite ends of each of said elongated TiO₂crystallites extend outwardly and terminate at an angle normal to the outer surface forming said spherical structure.

9. Rutile TiO₂microparticles which comprise generally spherical structures in the range of from 1 to 2 microns in diameter, said spherical structures comprising ordered acicular aggregates of elongated TiO₂crystallites, produced by the process comprising:

(a) forming an aqueous solution of a soluble titanium compound at a titanium concentration of from 0.5 to 1.0 moles per liter;

(b) introducing a morphology controlling agent selected from the group consisting of an α-hydroxy carboxylic acid of the formula R—CH(OH)COOH, an α-hydroxy carboxamide of the formula R—CH(OH)CONH₂or an α-amino acid of the formula R—CH(NH₂)COOH, wherein R is an alkane, alkene, alkyne, arene, or cycloalkane group having 4 or fewer carbon atoms, into the solution at an acid- or carboxamide-to-titanium molar ratio of from 0.02 to 0.2 while simultaneously heating the solution to a temperature in the range of from 75° C. to 80° C. with constant stirring;

(c) maintaining the stirred solution at a temperature in the range of from 75° C. to 80° C. for a period of from one to 3 hours;

(d) elevating the temperature of the stirred solution to a value of from 100° C. to the refluxing temperature and maintaining said temperature for a period of from 2 hours to 4 hours to form a reaction product;

(e) optionally neutralizing the reaction mixture which results from step (e);

(f) cooling the reaction mixture to room or ambient temperature; and

(h) separating and drying the reaction product.

10. The rutile TiO₂microparticles of claim 9 wherein said elongated TiO₂crystallites have a length of from 20 nm to 50 nm and a thickness of from 3 nm to 5 nm.

11. The rutile TiO₂microparticles of claim 10 wherein one of the ends from each of said elongated TiO₂crystallites assemble into a cluster whereby the opposite ends of each of said crystallites extend outwardly and terminate at an angle normal to the outer surface forming said spherical structure.

12. The rutile TiO₂microparticles of claim 9 wherein said morphology controlling agent is selected from lactic acid (CH₃CH(OH)COOH); 2-hydroxybutyric acid (C₂H₅CH(OH)COOH); 2-hydroxypentanoic acid (C₃H₇CH(OH)COOH); 2-Hydroxyhexanoic acid (C₄H₉CH(OH)COOH); 2-Hydroxyisocaproic acid (CH₃CH(CH₃)CH₂CH(OH)COOH); alanine (CH₃CH(NH₂)COOH); valine (CH₃CH(CH₃)CH(NH₂)COOH); norvaline (C₃H₇CH(NH₂)COOH); isoleucine (C₂H₅CH(CH₃)CH(NH₂)COOH); leucine (CH₃CH(CH₃)CH₂CH(NH₂)COOH); and norleucine (C₄H₉CH(NH₂)COOH) and mixtures thereof.

13. The rutile TiO₂microparticles of claim 9 wherein said soluble titanium compound is selected from titanium oxychloride (TiOCl₂), titanium oxybromide (TiOBr₂), titanium oxyiodide (TiOI₂), titanium oxynitrate (TiO(NO₃)₂), titanium trichloride (TiCl₃), titanium tribromide(TiBr₃), titanium oxalate (Ti₂(C₂O₄)₃), potassium hexafluorotitanate(K₂TiF₆), ammonium hexafluorotitanate ((NH₄)₂TiF₆), potassium titanyloxolate (K₂TiO(C₂O₄)₂), ammonium titanyloxolate ((NH₄)₂TiO(C₂O₄)₂), titanium bis(ammonium lactate) dihydroxide ([CH₃CH(O)COONH₄]₂Ti(OH)₂) and mixtures thereof.

14. The rutile TiO₂microparticles of claim 12 wherein said soluble titanium compound is selected from titanium oxychloride (TiOCl₂), titanium oxybromide (TiOBr₂), titanium oxyiodide (TiOI₂), titanium oxynitrate (TiO(NO₃)₂), titanium trichloride (TiCl₃), titanium tribromide(TiBr₃), titanium oxalate (Ti₂(C₂O₄)₃), potassium hexafluorotitanate(K₂TiF₆), ammonium hexafluorotitanate ((NH₄)₂TIF₆), potassium titanyloxolate (K₂TiO(C₂O₄)₂), ammonium titanyloxolate ((NH₄)₂TiO(C₂O₄)₂), titanium bis(ammonium lactate) dihydroxide ([CH₃CH(O)COONH₄]₂Ti(OH)₂) and mixtures thereof.

15. The rutile TiO₂microparticles of claim 14 wherein said morphology controlling agent is lactic acid (CH₃CH(OH)COOH), and said soluble titanium compound is titanium oxychloride (TiOCl₂).

16. A method for preparing rutile TiO₂particles which comprise structures in a botryoidal morphology having a size in the range of from 10 to 20 microns, said structures being aggregates of elongated TiO₂crystallites having a thickness of from 3 nm to 5 nm, said method comprising:

(b) introducing a morphology controlling agent selected from an α-hydroxy carboxylic acid of the formula R—CH(OH)COOH, an a-hydroxy carboxamide of the formula R—CH(OH)CONH₂or an a-amino acid of the formula R—CH(NH₂)COOH, wherein R is an alkane, alkene, alkyne, arene, or cycloalkane group having 4 or fewer carbon atoms, into the solution at an acid- or carboxamide-to-titanium molar ratio of from 0.02 to 0.2 while simultaneously heating the solution to a temperature in the range of from 75° C. to 80° C. with constant stirring;

(c) introducing TiO₂seeds into the stirred solution at a seed-to-TiO₂molar ratio of from 0.0005 to 0.0015 and maintaining the stirred solution at a temperature in the range of from 75° C. to 80° C. for a period of from one to 3 hours;

(e) optionally neutralizing the reaction mixture resulting from step (d);

(f) cooling the reaction mixture to room or ambient temperature; and

(g) separating and drying the reaction product.

17. The method of claim 16 wherein said morphology controlling agent is selected from lactic acid (CH₃CH(OH)COOH); 2-hydroxybutyric acid (C₂H₅CH(OH)COOH); 2-hydroxypentanoic acid (C₃H₇CH(OH)COOH); 2-Hydroxyhexanoic acid (C₄H₉CH(OH)COOH); 2-Hydroxyisocaproic acid (CH₃CH(CH₃)CH₂CH(OH)COOH); alanine (CH₃CH(NH₂)COOH); valine (CH₃CH(CH₃)CH(NH₂)COOH); norvaline (C₃H₇CH(NH₂)COOH); isoleucine (C₂H₅CH(CH₃)CH(NH₂)COOH); leucine (CH₃CH(CH₃)CH₂CH(NH₂)COOH); and norleucine (C₄H₉CH(NH₂)COOH) and mixtures thereof.

18. The method of claim 16 wherein said soluble titanium compound is selected from titanium oxychloride (TiOCl₂), titanium oxybromide (TiOBr₂), titanium oxyiodide (TiOI₂), titanium oxynitrate (TiO(NO₃)₂), titanium trichloride (TiCl₃), titanium tribromide(TiBr₃), titanium oxalate (Ti₂(C₂O₄)₃), potassium hexafluorotitanate(K₂TiF₆), ammonium hexafluorotitanate ((NH₄)₂TiF₆), potassium titanyloxolate (K₂TiO(C₂O₄)₂), ammonium titanyloxolate ((NH₄)₂TiO(C₂O₄)₂), titanium bis(ammonium lactate) dihydroxide ([CH₃CH(O)COONH₄]₂Ti(OH)₂) and mixtures thereof.

19. The method of claim 17 wherein said soluble titanium compound is selected from titanium oxychloride (TiOCl₂), titanium oxybromide (TiOBr₂), titanium oxyiodide (TiOI₂), titanium oxynitrate (TiO(NO₃)₂), titanium trichloride (TiCl₃), titanium tribromide(TiBr₃), titanium oxalate (Ti₂(C₂O₄)₃), potassium hexafluorotitanate(K₂TiF₆), ammonium hexafluorotitanate ((NH₄)₂TiF₆), potassium titanyloxolate (K₂TiO(C₂O₄)₂), ammonium titanyloxolate ((NH₄)₂TiO(C₂O₄)₂), titanium bis(ammonium lactate) dihydroxide ([CH₃CH(O)COONH₄]₂Ti(OH)₂) and mixtures thereof.

20. The method of claim 19 wherein said morphology controlling agent is lactic acid (CH₃CH(OH)COOH), and said soluble titanium compound is titanium oxychloride (TiOCl₂).

21. Rutile TiO₂microparticles comprising structures in a botryoidal morphology having a size in the range of from 10 to 20 microns and formed by the process of:

(b) introducing a morphology controlling agent selected from an α-hydroxy carboxylic acid of the formula R—CH(OH)COOH, an α-hydroxy carboxamide of the formula R—CH(OH)CONH₂or an α-amino acid of the formula R—CH(NH₂)COOH, wherein R is an alkane, alkene, alkyne, arene, or cycloalkane group having 4 or fewer carbon atoms, into the solution at an acid- or carboxamide-to-titanium molar ratio of from 0.02 to 0.2 while simultaneously heating the solution to a temperature in the range of from 70° C. to 80° C. with constant stirring;

(c) introducing TiO₂seeds into the stirred solution at a seed-to-TiO₂molar ratio of from 0.0005 to 0.0015 and maintaining the stirred solution at a temperature in the range of from 70° C. to 80° C. for a period of from one to 3 hours;

(d) maintaining the stirred solution at a temperature in the range of from 70° C. to 80° C. for a period of from one to 3 hours;

(e) elevating the temperature of the stirred solution to a value of from 100° C. to the refluxing temperature and maintaining said temperature for a period of from 2 hours to 4 hours to form a reaction product;

(f) optionally neutralizing the reaction mixture resulting from step (e);

(g) cooling the reaction mixture to room or ambient temperature and separating and drying the reaction product.

22. The rutile TiO₂microparticles of claim 21 wherein:

(a) said morphology controlling agent is selected from lactic acid (CH₃CH(OH)COOH); 2-hydroxybutyric acid (C₂H₅CH(OH)COOH); 2-hydroxypentanoic acid (C₃H₇CH(OH)COOH); 2-Hydroxyhexanoic acid (C₄H₉CH(OH)COOH); 2-Hydroxyisocaproic acid (CH₃CH(CH₃)CH₂CH(OH)COOH); alanine (CH₃CH(NH₂)COOH); valine (CH₃CH(CH₃)CH(NH₂)COOH); norvaline (C₃H₇CH(NH₂)COOH); isoleucine (C₂H₅CH(CH₃)CH(NH₂)COOH); leucine (CH₃CH(CH₃)CH₂CH(NH₂)COOH); and norleucine (C₄H₉CH(NH₂)COOH) and mixtures thereof, and

(b) said soluble titanium compound is selected from titanium oxychloride (TiOCl₂), titanium oxybromide (TiOBr₂), titanium oxyiodide (TiOI₂), titanium oxynitrate (TiO(NO₃)₂), titanium trichloride (TiCl₃), titanium tribromide(TiBr₃), titanium oxalate (Ti₂(C₂O₄)₃), potassium hexafluorotitanate(K₂TiF₆), ammonium hexafluorotitanate ((NH₄)₂TiF₆), potassium titanyloxolate (K₂TiO(C₂O₄)₂), ammonium titanyloxolate ((NH₄)₂TiO(C₂O₄)₂), titanium bis(ammonium lactate) dihydroxide ([CH₃CH(O)COONH₄]₂Ti(OH)₂) and mixtures thereof.

23. Rutile TiO₂microparticles in a botryoidal morphology having a size in the range of from 10 to 20 microns which comprise an assembly of generally spherical structures in the range of from 1 to 2 microns in diameter, said spherical structures comprising ordered acicular aggregates of elongated TiO₂crystallites having a thickness in the range of from 3 nm to 5 nm in which one end of each of said elongated TiO₂crystallites are joined into a cluster such that the opposite ends of each of said elongated TiO₂crystallites extend outwardly and terminate at an angle normal to the outer surface forming said spherical structure.