Process for the preparation of titanium dioxide nanorods

Abstract

The present invention relates to a process for preparing high aspect ratio titanium dioxide (TiO.sub.2) nanorods using a one-pot hydrothermal technique. Reaction additives of oxalic acid and sodium hydroxide (NaOH) are used to promote the conversion of titanium dioxide precursors, preferably tetraisopropoxide (TTIP), into a one-dimensional TiO.sub.2 morphology.

Claims

1. A process for the preparation of TiO.sub.2 nanorods, comprising the reaction of a titanium dioxide precursor with oxalic acid and an alkali metal hydroxide.

2. The process of claim 1, wherein the alkali metal hydroxide is NaOH.

3. The process of claim 1, wherein the titanium dioxide precursor is selected from the group consisting of: titanium alkoxide, titanium halide, titanium tetrachloride, titanylsulphate, titanyl bis(acetylacetonate), titanium alkoxide, titanium tetramethoxide, titanium tetraethoxide, titanium tetra n-propoxide, titanium tetraisopropoxide (TTIP), titanium tetra n-butoxide and titanium tetra i-butoxide.

4. The process of claim 3, wherein the titanium dioxide precursor is titanium tetraisopropoxide (TTIP).

5. The process of claim 1, wherein the process is a hydrothermal one-pot synthesis.

6. The process according to claim 1, wherein the nanorods have an aspect ratio in the range of about 30 to about 200.

7. The process of claim 1, wherein the process comprises first reacting the oxalic acid with the titanium dioxide precursor to form a titanium oxalate solution in a reactor and subsequently adding the alkali metal hydroxide to the reactor, wherein the alkali metal hydroxide is NaOH.

8. The process of claim 7, wherein during the addition of the NaOH the reactor is continuously stirred.

9. The process of claim 8, wherein after the alkali metal hydroxide is added to the reactor, further comprising the step of heating of the reactor to a temperature in the range of about 100 to about 300° C.

10. The process of claim 9, further comprising the step of cooling the product and rinsing the product with water and/or an acid.

11. The process of claim 10, wherein the product was sequentially rinsed with acid and water.

12. The process of claim 10, wherein the acid is selected from the group consisting of hydrochloric, nitric and sulfuric.

13. The process of claim 11, further comprising the step of annealing the product at temperatures ranging from about 300 to about 1100° C.

14. The process of claim 13, wherein the step of annealing the product is at a temperature in the range of 700° C. to 900° C. to form an anatase form of the TiO.sub.2 nanorods.

15. The process of claim 13, wherein the step of annealing the product is at a temperature of about 1100° C. to form a rutile form of the TiO.sub.2 nanorods.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1A is a SEM image showing high aspect ratio TiO.sub.2 nanorods were obtained when oxalic acid, NaOH, TTIP, and H.sub.2O were present in accordance with the teachings of the present invention.

(2) FIG. 1B is a SEM image showing spiked spherical particles were obtained when NaOH, TTIP and H.sub.2O were present in a comparative example.

(3) FIG. 1C is a SEM image showing that short TiO.sub.2 nanorods were obtained when NaOH, TTIP, and H.sub.2O were present in a comparative example.

(4) FIG. 1D is a SEM showing that amorphous TiO.sub.2 was obtained when only TTIP and H.sub.2O were present in a comparative example.

(5) FIG. 1E is a SEM showing that TiO.sub.2 flakes/plates were obtained when oxalic acid, NaOH, TTIP, and H.sub.2O were present and when the reaction was performed at room temperature in a comparative example.

(6) FIG. 1F is a SEM showing that TiO.sub.2 porous matrix was obtained when TTIP and H.sub.2O were present and when the reaction was performed at room temperature in a comparative example.

(7) FIG. 2A. is a graph of XRD patterns of TiO.sub.2 nanorods as a function of annealing temperature.

(8) FIG. 2B. is a graph of XRD pattern of TiO.sub.2 spiked spheres with no subsequent annealing. Anatase (o) and rutile (*) phases are denoted.

DETAILED DESCRIPTION

(9) Reference will now be made in greater detail to a preferred embodiment of the invention, an example of which is illustrated in the accompanying drawings. Wherever possible, the same reference numerals will be used throughout the drawings and the description to refer to the same or like parts.

(10) The terms “titanium dioxide precursor” or “precursor”, herein used indifferently, refer to inorganic or organic titanium-containing compounds that that can form TiO.sub.2 by means of known reactions, e.g. hydrolysis. Non-limiting examples of titanium dioxide precursor include for instance: titanium alkoxide, titanium halide, such as titanium tetrachloride, titanylsulphate, titanyl bis(acetylacetonate). Preferably, though not exclusively, the precursor is a titanium alkoxide, i.e. a compound Ti(OR).sub.4, wherein R is a C.sub.1-C.sub.6 alkyl group, e.g., titanium tetramethoxide, titanium tetraethoxide, titanium tetra n-propoxide, titanium tetraisopropoxide, titanium tetra n-butoxide and titanium tetra i-butoxide. Particularly preferred is titanium tetraisopropoxide.

(11) The term “nanorods” refers to non-spherical, elongated particles, having a typical rectangular section when observed by SEM.

(12) The process of the present invention comprises reacting a titanium precursor with aqueous oxalic acid in a molar ratio comprised between 1:1 and 1:5, preferably between 1:2 and 1:4, and most preferably 1:2 to form a titanium oxalate solution. NaOH is added to the titanium oxalate solution. Suitable ranges of NaOH concentrations are about 0.5M to about 1.5M by weight prior to hydrothermal treatment. The reaction can be carried out as a one-pot hydrothermal synthesis.

(13) In one embodiment, the titanium oxalate solution is formed in a reactor. NaOH pellets can be added over time to the reactor with magnetic stirring. The reaction mixture is continuously stirred for a pre-determined time until the NaOH is fully dissolved. The reactor can be sealed and heated. In one embodiment, the vessel is placed in an oven at a temperature in the range of about 100° C. to about 200° C., preferably 150° C. Upon cooling, the product can be sequentially rinsed with an acid and water. Suitable acids include hydrochloric acid, nitric acid and sulfuric acid. The washed product is dried, such as at a temperature of about 50° C. to about 150° C., preferably 100° C.

(14) The products were characterized by X-ray diffraction (XRD) and scanning electron microscopy. The results show that the starting titanium precursor was fully converted into nanomaterials with a lamellar titanate structure having the general formula Na.sub.xH.sub.2-xTi.sub.3O.sub.7nH.sub.2O. The resulting product formed was linear crystals of TiO.sub.2 having nanorod characteristics and an aspect ratio in the range of about 30 to about 200.

(15) The process of the present invention is distinguished by an improved, single-stage process procedure which dispenses with any intermediate isolation or intermediate purification stages, hereinafter referred to as “one-pot synthesis”. The single-stage preparative process comprises, for the purposes of the present invention, the preparation of the TiO.sub.2 nanotubes without any isolation of intermediates. The present invention therefore describes a process in which the target product is prepared in-situ from the starting materials in one reactor without costly and time-consuming intermediate isolations or intermediate purifications.

(16) The invention can be further illustrated by the following examples thereof, although it will be understood that these examples are included merely for purposes of illustration and are not intended to limit the scope of the invention unless otherwise specifically indicated. All percentages, ratios, and parts herein, in the Specification, Examples, and Claims, are by weight and are approximations unless otherwise stated.

EXPERIMENTS

(17) Oxalic acid, titanium tetraisopropoxide (TTIP), and sodium hydroxide pellets (NaOH) were obtained from Sigma Aldrich, Alfa Aesar, and Fisher Scientific, respectively. Additionally, 18.2 MΩ deionized water, obtained from a Millipore Direct-Q 5 system, was used in all experiments.

(18) In a typical synthesis, titanium oxalate was first prepared by reacting TTIP with 0.364 M aqueous oxalic acid in a 1:2 molar ratio. Next, while magnetically stirring, 16 g of NaOH pellets were slowly added to a 125 mL Teflon-lined stainless steel autoclave containing 40 mL of the titanium oxalate solution. After ten minutes of continuous stirring, the NaOH was fully dissolved to and a gel-like consistency was observed. Next, the reaction vessel was tightly sealed and placed in an oven for 48 h at 150° C. Upon cooling, the product was sequentially rinsed with 1.0 L of 0.1 M HCl and 1.0 L of H.sub.2O. Finally, the washed product was dried at 100° C. for 12 h yielding TiO.sub.2 nanorods. All products were placed in a porcelain crucible and annealed in air, in a muffle furnace at temperatures ranging from 300-1100° C.

(19) Powder X-ray diffraction (XRD) patterns of the products were recorded on a Panalytical X'Pert Pro diffractometer with Xcelerator, using Cu Kα radiation (λ=1.5406 Å) at 45 kV and 40 mA. Scanning electron microscopy (SEM) images of the products were obtained using a JEOL JCM-5700 Scanning Electron Microscope. Samples were supported on double-sided carbon tape and sputter coated with gold prior to analysis. The instrument was operated in high vacuum mode using accelerating voltages of 2-15 kV at nominal working distances of 7-12 mm. Elemental analysis was also performed using energy-dispersive X-ray spectroscopy (EDX), which was an accessory to the JEOL JCM-5700 SEM. Comparative examples were performed with the following combinations of additives being present: oxalic acid, TTIP, and H.sub.2O; NaOH, TTIP, and H.sub.2O; TTIP and H.sub.2O; NaOH, TTIP, and H.sub.2O; and TTIP and H.sub.2O.

(20) High-aspect ratio nanorods with an average diameter of 160 nm and a major dimension ranging from 5-40 μm were formed using a one-pot synthesis containing TTIP, oxalic acid, and sodium hydroxide in accordance with the teachings of the present invention, as shown in FIG. 1A. Numerous comparative experiments were subsequently conducted. First, NaOH was omitted from the reaction vessel, while keeping all other experimental parameters the same. This comparative experiment yielded spiked spherical particles as demonstrated in the SEM image shown in FIG. 1B. A second comparative experiment involved the omission of oxalic acid from the reaction vessel, while keeping all other experimental parameters the same. This experiment yielded shorter nanorods as demonstrated in FIG. 1C. Inspection of the experimental parameters used to generate FIGS. 1A-IC indicate that NaOH is a prerequisite for the formation of rod shape morphologies, while oxalic acid in conjunction with NaOH is useful to further elongate the rods.

(21) A comparative example was performed with the omission of both oxalic acid and NaOH from the reaction vessel. This experiment yielded spherical and largely amorphous particle morphologies, as demonstrated in the SEM image shown in FIG. 1D. This result confirmed the impact of both NaOH and oxalic acid on inducing non-spherical geometries.

(22) Comparative examples were performed to investigate the impact of reaction vessel temperature, both in the presence and absence of both oxalic acid and NaOH. When oxalic acid and NaOH were present, an ambient reaction temperature interestingly yielded non-spherical platelet-structures as shown in FIG. 1E. The capacity of oxalic acid and NaOH to induce non-spherical geometry was still observed, albeit to a lesser extent. It was found that temperature, in conjunction with oxalic acid and NaOH, play a critical role in the elongation and formation of rod structures.

(23) A comparative example was performed in which heat, oxalic acid, and NaOH were omitted from the reaction vessel, a porous matrix of largely spherical particles was observed as shown in FIG. 1F. This morphology is consistent with the morphology that is commonly observed when TiO.sub.2 is fabricated using a sol-gel chemistry approach.

(24) The XRD patterns for the high aspect ratio TiO.sub.2 nanorods are provided in FIG. 2A. Anatase (o) and rutile (*) phases are denoted. The patterns in FIG. 2A represent the various temperatures at which the nanorods were annealed. Inspection of FIG. 2A clearly demonstrates that for annealing temperatures up to 500° C., an amorphous titanium oxalate type crystal structure was observed, i.e. there were no clear indications that either the anatase or rutile forms of TiO.sub.2 were present. The anatase crystal form of TiO.sub.2 began to appear at an annealing temperature of 700° C. XRD patterns associated with the rutile form of TiO.sub.2 began to appear at an annealing temperature of 900° C., with anatase still being predominant. Finally, the rutile form was dominant at an annealing temperature of 1100° C.

(25) FIG. 2B provides the XRD patterns of the spiked spheres shown in FIG. 1B obtained when NaOH was omitted from the reaction. The XRD spectra revealed the strong presence of the rutile crystal form of TiO.sub.2, despite the fact no subsequent annealing was performed. These results are consistent with other results as described in [25], where the rutile form of TiO.sub.2 was obtained in the presence of the oxalate ion, specifically when the molar ratio R=[oxalate]/[Ti.sup.4+]=2.

(26) It is to be understood that the above-described embodiments are illustrative of only a few of the many possible specific embodiments, which can represent applications of the principles of the invention. Numerous and varied other arrangements can be readily devised in accordance with these principles by those skilled in the art without departing from the spirit and scope of the invention.