DOI: 10.17533/udea.redin.n78a08

ARTÍCULO ORIGINAL

Colour evolution of the oxide layer formed on the Au-25Fe AND Au-24.5Fe-0.5Co alloys

Evolución del color de la capa de óxido formada en las aleaciones Au-25Fe y Au-24.5Fe-0.5Co

¹Facultad de Ingeniería, Universidad de Antioquia. Calle 67 # 53-108. A. A. 1226. Medellín, Colombia.

²Facultad de Ciencias Exactas y Naturales, Universidad de Antioquia. Calle 67 # 53-108. A. A. 1226. Medellín, Colombia.

* Corresponding author: Sandra Milena Restrepo Arcila, e-mail: sandra.restrepoa@udea.edu.co

(Received July 6, 2015; accepted January 28, 2016)

ABSTRACT

Keywords: Magnetite, oxide layer, coloured gold alloys, colour theory

RESUMEN

Se aplica la teoría del color propuesta por Heavens (1991) para el cálculo de los espesores de las películas delgadas de magnetita, Fe₃O₄, los cuales fueron obtenidos por tratamiento térmico a 250°C de una aleación de oro (Au-24.5Fe-0.5Co). Los espectros de reflectancia obtenidos de las muestras pulidas con diferentes grados de oxidación (y de color) fueron usados para calcular los índices de refracción (real) y de extinción (imaginario) del sustrato metálico (n₂, k₂) y de la capa de magnetita (n₁=2,42, k₁). La forma a+bλ+cλ² se tomó del ajuste de parámetros entre las curvas experimentales y teóricas. El ajuste de los datos resultan en desviaciones entre 2 y 10%, para los espesores en el rango de 0 nm (solo metal original) y 65 nm (color azul oscuro). Por medio de un modelo matemático siguiendo la teoría de Heavens, el espesor de cada capa ha sido predicho con alta precisión, utilizando las mediciones de reflectancia espectral. En consecuencia, proponemos que mediante el uso de esta metodología se pueden obtener fácilmente los valores de los coeficientes de extinción de las especies de óxido y, además, se pueden predecir los espesores de la capa de óxido. Los valores de espesores de la magnetita encontrados en la presente investigación están dentro del intervalo reportado en la literatura para la interferencia de primer orden en los aceros, desde el amarillo claro (~46 nm) hasta el azul (~72 nm).

Palabras clave: Magnetita, capa de oxidación, aleaciones de oro coloreadas, teoría del color

1. Introduction

The different colours, hues, and their variation with the angle of observation that are present in metallic alloys are an innovative feature for jewellery pieces. Furthermore, in the field of optics, it is quite known that the iridescence which originates from the optical thin films would generate stunning colours that will be appreciated by jewellery lovers, just like the iridescent effect formed in soap bubbles. When iron reacts with oxygen, an iron oxide, generally magnetite, (Fe₃O₄) is formed. In a minor proportion, hematite (Fe₂O₃), can also be formed. If this oxide is generated on the appropriate substrate, that is, one with sufficient iron, a layer of magnetite will cover the substrate. It is expected that the thickness of such layer will be dependent on the method applied to obtain the oxide. Iron oxides can be obtained in three ways: thermically (and then called frosted), chemically or electrochemically. The later, anodically oxidized in the presence of alkali [1] Table1, Figure 1.

This oxide layer filters light waves by reflection, producing brilliant colours. As the thickness of the oxide layer changes, so does its colour and appearance, producing outstanding iridescence.

Constable reports the following thicknesses for first-order interference colours in iron oxide layers [5]: pale yellow, 46 nm; reddish yellow, 52 nm; reddish brown, 58 nm; purple, 63 nm; violet, 68 nm; and blue, 72 nm. As the thickness grows, a reduction of glow is observed. A similar colour range is observed in other types of material layers formed by oxidation, such as TiO₂, SiO₂ and Si₃N₄ among others [5].

Colour variation can also be obtained by oxidation on a steel surface when the steel is heated at temperatures between 180°C and 427°C [6]. A typical colour scale is shown in Figure 2.

Several heat treatments have been reported on different alloys There is a patent concerning the production of intense blue coloured layers on a Au-24,5Fe-0,5Ni alloy, when treated at 450-600 °C between 10 and 15 minutes [7]. Antoniazzi also patented a treatment to produce iridescent blue on AuCrMoVCWFe alloys after a rather rapid treatment with flame [8, 9].

The aim of this study is to numerically determine the thicknesses of iron oxide thin films formed by heat treatment of the Au-24.5Fe-0.5Co alloy and their relationship with the measured colour by spectrophotometrical methods.

2. Experimental procedure

2.1. Alloy preparation

Refined gold was obtained by quartering and subsequent dissolution in nitric acid, HNO₃, (following ASTM E 1335 norm, method A) [10]. Iron (analytic grade) was purchased from J.J Baker Chemical Co (99.95% purity) and cobalt (micronized) was commercially obtained from Goodfellow Cambridge Ltd. (99.95% purity). Graphite crucibles coated with zirconia were used to avoid iron or cobalt contamination. Alloys were melted in a BEGO induction furnace in presence of an Argon inert atmosphere to avoid iron and cobalt oxidation during the process (Figure 3).

2.2. Surface characterization

A bifurcated probe of 200 µm diameter was used (Avantes optical fiber probe) to measure reflectance spectra of the metallic alloy samples with normal incidence. The probe was held on a micromanipulator with three degrees of freedom (3D movement) to be able to measure and compare different areas of the samples. A halogen and deuterium double light source was used (Avalight-DH-S-BAL) for deep UV and visible range respectively. Reflected light was captured and taken to an Avantes spectrophotometer (AvaSpec-2048). A first surface mirror was used as calibration standard.

The reflectance spectra obtained were normalized. The calculations of the thicknesses were made according to the colour theory proposed by Heavens [12]. The real part of the refraction index and the (imaginary) extinction coefficient of the metallic substrate (n₂, k₂) and the oxide layers (n₁, k₁) in the a+bλ+cλ² form were taken as adjusting parameters between experimental and theoretical curves. A fitting of the data with deviations between 2% and 10% for 0 nm (only substrate) and 61 nm (dark blue colour) thicknesses were found. The surfaces of the alloys were also characterized by micro-Raman spectroscopy by using a confocal Raman spectrometer (Horiba Jobin Yvon, model Labram HR). A laser He/Ne of 632 nm was used. The zones for micro-Raman analysis were observed using a Nikon BX41 focal microscope with plan achromatic objectives.

3. Results and analysis

Depending on the time of heat treatment applied to the Au alloy samples, different colours were obtained, ranging from ochre yellow (minimum time) to black (maximum time), through fuchsia, purple and blue. The thickness of the layers formed on the samples are so thin that it is impossible to measure them directly; therefore, colour theory is usually applied. Here, we have used the theory proposed by Heavens [12] to calculate the thickness of each oxide layer to ultimately being able to predict the colour of a given oxidation time. Two alloys were then treated as referred in section 2.1 (Au-24.5Fe-0.5Co and Au-25Fe, at 250°C, for a series of times). In this case, reflectance equations are deduced from the scheme shown in Figure 4.

The amplitude of incident and reflected waves are considered to be a function of Fresnell coefficients, r₁ and r₂, which correspond to the oxide layer and the metallic substrate, respectively. We reserve r₀ for air.

The resulting equations are presented as follows (Eqs. 1 and 2):

E₀⁺, E₁⁺, E₂⁺ are the amplitudes of the electric vectors of the incident (or transmitted) waves in the layers 1, 2 and 3. E₀^-, E₁^-, E₂^- the amplitudes of the electric vectors of the waves reflected on the layers 1, 2, 3 (here, E₂^- = 0).

n₀, n₁, n₂ are the complex refraction indices of layers 1, 2 and 3 (n_m = n_m-ik_m, with k₀ = 0)

r₁, r₂ are the Fresnel reflection coefficients of the light traveling through the layers 0→1 and 1→2 expressed as: r_m=g_m+ih_m in Eq. (3).

In r₁ and r₂ cases, real and imaginary coefficients are showed in Eqs. (4-7):

and by matrix product in Eqs. (9-12), it reduces to:

Reflectance is defined in Eq. (13), as:

In terms of energy of the reflected waves vs. incident in Eqs. (14-20):

n₂, k₂ parameter adjustments were made modeling the experimental with the theoretical result, under the presumption d=0 (without magnetite layer), resulting in Eqs. (21) and (22):

Figure 6 shows the reflectance curve measured in the spectrophotometer with modeling adjustment (1.7%) for Au-24.5Fe-0.5Co alloy without superficial oxide layer.

Once the constant parameters, n₁ and k₁, of the substrate were obtained, their values were introduced in the model to calculate the oxide layer parameters, n₂ and k₂. The obtained value for the real part (n₂ = 2.48 in Eq. (23)) is in remarkably good agreement with that reported in reference [4] (n between 2.42 and 3.0 for oxides with concentrations around 95% magnetite). The extinction coefficient, k₁, is, according to Eq. (24):

Figure 7 shows the extinction coefficients of the magnetite formed in air-oxidation of the alloys Au-24.5Fe-0.5Co and carbon steel [13].

Different thickness results for coloured samples at different times of heat treatments (250°C) are shown in Figure 8 (a, b, c, d).

The calculated thickness values obtained after heat treatment were compared with those reported by other authors [13] obtained a magnetite in low carbon steels heated at 280 °C (for a 6 nm layer) and 485 °C (for a 98 nm layer). In agreement with our results in a gold alloy, obtained a magnetite layer after heat treatment on the steel surfaces. However, regarding the results shown in Figure 7, it can be seen that the values of the extinction coefficient are slightly different, probably because the base alloys are different. It must be highlighted that this author obtained the blue colour with a thickness of 98 nm (in carbon steel), whilst we obtained the same colour with 61 nm (in gold alloy).

The oxide thickness values that were found in this study fall in the interval reported for first-order interference in steels, from light yellow (46 nm) to blue (72 nm) [1, 2, 13].

In order to determine the type of oxide that constitutes the film, we performed Raman spectroscopy of all our samples.

Figure 9 shows the Raman spectra of the sample surfaces after heat treatment. As a confirmation of our expectations, all the spectra show the characteristic peak of magnetite (Fe₃O₄) near to 700 cm^-1 in both alloy systems. Furthermore, the presence of hematite (Fe₂O₃) is also observed, because of the pair of bands near to 400 and 1500 cm^-1. The difference in proportion between magnetite and hematite is evident from the very different intensity of the peaks, as already reported in the literature [3, 4]. Such behavior is observed in all the samples analyzed. On the other hand, regarding the analysis of the time of oxidation compared to the composition, we observed that the samples with a longer treatment corresponded to the highest spectra. In general, the higher the spectra, the longer the time.

4. Conclusions

The colour of both gold alloys is produced by the formation of a fine layer of superficial iron oxide (composed by magnetite and hematite). We have shown by using spectrophotometrical and material composition analyses that the colour of the alloys strongly rely on the thickness of the iron oxide layer, which will depend on the time of treatment. We have created oxide layers with colors that range from yellow (20 nm) to blue (61 nm) that are composed by –mostly– magnetite and also hematite.

In addition to the reported experimental analyses, we performed a theoretical study of the colours created by the thin layers formed when the alloys were put under heat treatment. Until now, the physical model described by Heavens was used only for low carbon-steel. We applied the theory to two distinct alloy systems and demonstrated its validity. Moreover, we were able to calculate the extinction coefficients for the substrates and for the layers by experimentally measuring the reflectance spectra of the samples. To our knowledge, this is the first time that these values are reported for gold alloys. We propose this method to be applied for any substrate in which colouration will be a result of an oxide layer plus the base colour of the alloy. Thus, the possibilities are very diverse in jewelry design.

5. Acknowledgments

This project was partially funded by "Estrategia de Sostenibilidad 2014-2015 de la Universidad de Antioquia".

6. References

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