Plasma-spray synthesis and characterization of ti-based nitride and oxide nanogranules

Plasma-spray synthesis and characterization of ti-based nitride and oxide nanogranules

Georgios S. E. Antipas^*

School of Mining Engineering and Metallurgy, National Technical University of Athens, Zografou Campus, Athens 15780, Greece

ABSTRACT

The synthesis of nanosized Ti-based nanogranules via plasma spraying is reported. The synthesis route involved use of both nitrogen and oxygen gases with varying results. In the case of nitrogen, a mixture of titanium nitrides were produced, yielding both the Ti₂N and the sub-stoichiometric TiN_0.61 compounds. In the case of oxygen, both the stoichiometric rutile and TiO ceramic phases were indexed. Based on EDS analysis, even fractional oxygen concentrations caused tungsten impurities which originated from the cathode electrode. The method yielded particle mass median sizes of the order of 15nm and the smallest particles detected were 5nm.

Keywords: TiN, TiO, plasma spraying, rapid quenching

Introduction

Titanium nitrides are low-cost coating materials of choice owing to their enhanced tribology and biocompatibility^1,2. Notable nanoscale titanium nitride applications are diverse, such as catalysts increasing durability in proton exchange membrane fuel cells³, prosthetic materials in total hip and knee replacements⁴ and utilization in medical tools⁵ such as vascular stents⁶ and, lately, plasmonic materials with improved optical properties in the visible and near-infrared regions^7,8. On the other hand, titanium oxides have also found very practical applications such serving as active coatings in self-cleaning window products⁹ but are probably best known for their photocatalytic¹⁰ and photoluminescence¹¹ properties; in particular, titanium oxide nanocrystals embedded in alumina have been lately applied in ultraviolet photocatalysis⁹.

The simultaneous synthesis of nanostructured titanium nitrides and oxides at relatively high production rates at controlled stoichiometries is a challenge. Nanostructured materials exhibit enhanced properties compared to the polycrystalline phase¹². For example, although metallic nanostructured alloys may be sintered at low temperatures they, nonetheless, show higher hardness and yield strength than polycrystalline equivalents¹³. There are various techniques available for making nm-sized particles and they invariably address the degree of agglomeration when bulk nanostructures or nm dispersions are desired¹⁴. Also, in order to manufacture nanostructured materials, it is necessary to control the particle size and chemical stoichiometry at the same time and this can typically by achieved by rapid solidification¹⁵, albeit not in a large (e.g. industrial) scale.

One of the alternative routes for increased production rates of nanosized materials may be through plasma spraying¹⁶, in which an arc generated torch achieves vaporization of a high purity precursor material. In this process, the interior of a chamber is maintained at a pressure of up to 20 kPa while the precursor material is vaporized by a non-consumable tungsten electrode shielded by a blanket of inert gas, the latter both protecting the electrode from oxidation and maintaining the plasma arc. The inert gas phase is directed into the metallic vapour by a water cooled nozzle attached to the torch. The consumable precursor material is in the form of a rod, typically with a diameter up to 5 cm, fed horizontally or vertically relative to the non-consumable electrode; it is also electrically grounded and cooled by a copper anode and able of both translational and rotational motion. Homogeneous gas injection is achieved by the use of close-coupled gas injection nozzles^17-19. However, with increasing production rates (and, hence, with increasing vapour density¹⁹), both the gas flow rate and location of injection become important. The reaction gas can be introduced either together with the quench gas or separately in order to form an oxide, carbide or nitride from the metallic or semiconducting precursor material.

Introducing the reaction gas with the quench gas into the plasma allows the synthesis of a higher melting-point material, which enhances quenching and facilitates formation of nanocrystal particles. Also, by using a dissociable gas, for example, H₂ or N₂, along with the working gas allows the plasma to reach a higher temperature, producing a more complete reaction of the precursor vapour. Here, a number of Ti-based nanogranules are produced by plasma spraying with nitrogen and oxygen mixtures and their properties are discussed in terms of the main operating variables of the process with the aim of highlighting aspects of the effect of the flowrate and type of atomizing gas injected into the plasma reaction zone on granule size.

Material and Methods

In separate experiments, titanium metal vapour produced by plasma spraying was brought in contact with nitrogen and oxygen gases toward formation of TiN and TiO₂ nanogranules, respectively. The plasma spray facility used in this study is shown in Figure 1. The facility comprised four main control volumes. The upper volume (Figure 1a) contained the plasma spray and atomizer setup and consisted of the plasma arc and the gas injection nozzles, where introduction of the atomizing gas was at an angle from the vertical direction. The first stage of the process consisted of vaporization of a Ti rod by a tungsten inert gas (TIG) wrapped in a stream of Argon and cooled by a continuous flow of water, under ambient pressure conditions. The Ti rod was cooled by a Cu plate anode (see Figure 1a). The Argon flow shields against oxidation of the non consumable tungsten electrode and, further downstream, serves as an ionizing medium for the creation of the plasma arc. Introduction of the atomizing assembly was at an angle from the vertical direction so as to achieve an elongated plasma tail. Both Nitrogen and Oxygen flows were used as the quench/reaction medium. Both the quench/reaction and working gas flows were monitored by flow meters and were constantly regulated.

Upon atomization, gas expansion induced further cooling of the two-phase flow¹⁹; the expanding turbulent flow was then confined by a collecting cone (see Figure 1b) which was intended to hinder the material's in-flight agglomeration.

The two phase flow was then continuously recirculated between the collecting cone (Figure 1b) and the adjacent filtering compartment (see Figure 1c) by an ambient air flow maintained by a fan blower. The purpose of this stage was to withhold weakly segregated nanoparticles, separating them from the rest of the flow, which then consisted of nitride (oxide) powders. The latter were then routed into a storage compartment (see Figure 1d) through a collecting cone. A close up schematic of the plasma spraying nozzle is shown in Figure 1d.

The most critical operational parameters of the process were the point of gas injection and the degree of dilution of the nanocrystal aerosol. These parameters affected average particle size, size distribution and the degree of agglomeration.

A number of experiments were carried out for the determination of the effect of the gas flowrate on the size of Ti particles in a nitrogen flow. In addition, two nanocrystal synthesis experiments were performed for the study of particles via electron microscopy. In the latter experiments, a metallic Ti rid with a diameter of 7.5 cm (purity 99.99%) was used as the arc anode. Nitrogen gas injected at a rate of 14m³/h interacted with the Ti metal vapour towards formation of nitrides. Quench N₂ gas at a flux of 36m³/h was then injected to further cool the particles and prevent hard agglomeration. In a second experiment, Ti metal powder was mixed in a 50 wt.% ratio with Ti oxide powder. The powders were then compacted into a rod 7.5 cm in diameter by pressing and sintering. The rod was electrically conductive and used as an anode in a transferred arc. The anode was evaporated by the arc and the anode vapour was injected at an approximate rate of 200 g/h into the plasma. Following this, oxygen was injected into the plasma at a flowrate of 35m³/h to mediate cooling, finally yielding metal-oxide ceramic particles. Quench nitrogen gas (30m³/h) was later added to further cool the particles and prevent hard agglomeration. In both experiments, the cathode was a tungsten electrode shielded by a flow of 4m³/h of argon working gas combined with nitrogen and hydrogen at a volume ratio of 2:2:1 respectively. The applied electric current was 750 A.

X-ray diffraction (XRD) spectra were recorded on a Bruker D8-Focus diffractometer with nickel-filtered Cu-Ka radiation (l=1.5405 Å), operating at 40 kV and 40 mA. Sample cross sections were examined by scanning electron microscopy (SEM) on a Jeol 6380LV SEM, which also recorded energy dispersive X-ray spectra (EDS). Transmission electron microscopy (TEM) studies were performed on a Jeol 2100 HR microscope; TEM samples were prepared by forming a suspension of the particles with a concentration of between 0.1 and 0.01 wt% solid fraction. Nanocrystalline powder size distributions were measured with a Malvern Mastersizer.

Results and Discussion

XRD spectra for the Ti-N and Ti-O based materials are shown in Figure 2a and 2b, respectively. As seen, two distinct phases were formed in the plasma reaction zone depending on the working gas used. In the first case (see Figure 2a), Ti vapour interaction with the nitrogen gas yielded a mixture of titanium nitrides. In more detail, the Ti-N peak at 37 degrees was indexed as a mixture of Ti₂N and the sub-stoichiometric compound TiN_0.61, while 42.89 and 62.51 was mapped to the TiN_0.61 phase. On the other hand, the principal Ti-O peak at 24.76 degrees (see Figure 2b) was indexed as a mixture of Ti₃O₅ and Ti₉O₁₇, generally off-stoichiometric phases of TiO₂ rutile. The rest of the Ti-O peaks were found to be a mixture of stoichiometric rutile and TiO, the latter contributing more towards peaks found higher than 60 degrees 2 theta.

Figure 3 shows EDS of material made both in the presence of 0.5 w.t.% oxygen as well as in the absence of the oxygen gas. From the EDS spectra, it became evident that even fractional oxygen concentrations may cause tungsten impurities at levels of roughly 1.0w.t.% in the intermetallic phases. A typical dispersion of Ti-N intermetallics is shown in Figure 4.

Ti plasma-generated vapour reacting solely with nitrogen formed TiN nanocrystals of average size in the range 8-25 nm. Similarly, the Ti vapour interacting with oxygen gas formed TiO₂ nanocrystals (also see XRD analysis) of average sizes in the range 5-40 nm. Figure 5a shows the agglomerate particle size versus the gas flow injected into the nozzle under the applied back pressure, where it can be seen that (due to compressibility of the gas phase) the overall trend is one of decreasing particle size with increasing flowrate. As explained elsewhere^19,20, there is a transition of the liquid globule break up mechanisms with increasing density (or speed) of the gas phase from the 'bag' to 'the stripping' mode; this transition is in effect revealed by the change of curvature of the plot in Figure 5a. Also, in the Ti vapour/gas two-phase flow, there was a minimum achievable size, of the order of 15nm (d₅₀ mass median size), regardless of the increase in the speed of the gas phase, again as shown by the tailing off of the plot in Figure 5a. The distribution of particle sizes for the case of the Ti-N system is presented in Figure 5b, as measured by the size analyser. Overall, the effect of the radial injection point of the gas upon the nanocrystalline particle diameter followed the gas density and was on par with gas compressibility as previously calculated in the case of two-phase flows^17-19,21. When argon was used as the working gas and oxygen as the reaction gas, an oxygen-deficient oxide nanocrystal was formed, as detected by X-ray diffraction (see Figure 1a), while sub-stoichiometric material required further processing for complete oxidation; such post processing involved annealing of the powders in ambient conditions. This step was often found increase the degree of agglomeration and also caused an increase of particle size. Agglomeration appeared rather sensitive to the exact gas injection point inside the plasma chamber, as well as to the type of gas injected and to the gas flow rate. On the other hand, the presence of hydrogen in the working gas invariably led to the formation of water vapours and caused oxidation of the resulting nanoparticles. Further cooling led to the formation of metal-oxide ceramic particles due to the presence of oxygen and the high temperatures involved. Air quenching by a flow of 36m³/h added to cool the particles were also observed to prevent agglomeration. The nanocrystalline powders collected were typically found to have primary aggregate sizes of 50 nm and typical agglomerate sizes are 100 nm (also see Figure 4).

Conclusions

• Plasma spraying of Ti-based vapors yielded nanogranules. Nanogranule stoichiometry was difficult to control and ranged substantially.

• The synthesis method may provide the basis for larger production as compared to sheer laboratory-grade methods.

Received: November 13, 2013; Revised: July 24, 2014

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Publication Dates

• Publication in this collection
  15 Aug 2014
• Date of issue
  Oct 2014

History

• Accepted
  24 July 2014
• Received
  13 Nov 2013