Corrosion Analysis of an Experimental Noble Alloy on Commercially Pure Titanium Dental Implants

Corrosion Analysis of an Experimental Noble Alloy on Commercially Pure Titanium Dental Implants

The Open Dentistry Journal 21 Sep 2016 RESEARCH ARTICLE DOI: 10.2174/1874210601610010486



To determine whether the Noble Bond® Argen® alloy was electrochemically suitable for the manufacturing of prosthetic superstructures over commercially pure titanium (c.p. Ti) implants. Also, the electrolytic corrosion effects over three types of materials used on prosthetic suprastructures that were coupled with titanium implants were analysed: Noble Bond® (Argen®), Argelite 76sf +® (Argen®), and commercially pure titanium.

Materials and Methods:

15 samples were studied, consisting in 1 abutment and one c.p. titanium implant each. They were divided into three groups, namely: Control group: five c.p Titanium abutments (B&W®), Test group 1: five Noble Bond® (Argen®) cast abutments and, Test group 2: five Argelite 76sf +® (Argen®) abutments. In order to observe the corrosion effects, the surface topography was imaged using a confocal microscope. Thus, three metric parameters (Sa: Arithmetical mean height of the surface. Sp: Maximum height of peaks. Sv: Maximum height of valleys.), were measured at three different areas: abutment neck, implant neck and implant body. The samples were immersed in artificial saliva for 3 months, after which the procedure was repeated. The metric parameters were compared by statistical analysis.


The analysis of the Sa at the level of the implant neck, abutment neck and implant body, showed no statistically significant differences on combining c.p. Ti implants with the three studied alloys. The Sp showed no statistically significant differences between the three alloys. The Sv showed no statistically significant differences between the three alloys.


The effects of electrogalvanic corrosion on each of the materials used when they were in contact with c.p. Ti showed no statistically significant differences.

Keywords: Dental implants, Galvanic corrosion, Noble alloys, Noble bond®, Suprastructure, Titanium.


Due to their high cost, noble or semi-noble alloys with high content of gold and palladium, represent a problem when used to produce fixed prostheses over implants. Alternatively, newly developed alloys attempt to reduce corrosion without risk of losing the right physical properties. The different metallic materials used in such alloys have yielded varied results. Solá et al. [1] analysed resistance to corrosion of four noble alloys (Pontor 2®, Cerapall 2®, V-Gnathos Plus® and Pagalin®) and of a titanium alloy (Ti6Al4V) attached to commercially pure titanium (c.p. Ti). These authors observed a differential resistance to corrosion depending on the composition of each of the alloys used, despite the fact that all of them largely contain gold and palladium. For their part, as it has been shown, gold and palladium-based alloys present a lower dissolution rate and therefore greater corrosion resistance than those made up of non-noble base metals such as nickel- chrome or chrome-cobalt [2-6]. In order to improve corrosion resistance and “make them nobler” Sarantopoulos [7] studied two alloys (Noble Crown®and Noble Crown NF®) made with the last two pairs of non-noble metals to which palladium was added, thus he concluded that the inclusion of this element has deleterious effects upon the physico-chemical properties of both alloys. Furthermore, Poljak-Guberina [8] pointed out the need to study processes which may enable to line or coat non-noble materials with higher corrosion-resistance ones, which will improve the behaviour of these alloys in the oral environment. Electro-chemical corrosion is the most important injury factor in dental work. It produces unintended wear of the metal surface, and a deterioration of the outer and inner layers caused by exposure to chemicals or electrochemical reaction of the surrounding area [9].

Given the nature of the medium in the oral cavity, it is especially important that the materials used show a high electrolytic corrosion resistance. The consequences of corrosion in alloys for dental use may result in negative biological, functional and aesthetic effects, of which the biological ones have higher significance. During corrosive processes, metal ions are freed into the medium and come into contact with neighbouring tissues and/or are spread throughout the entire body. Biological incompatibility of these ions can produce body injury, causing toxicity and risk of sensitization; therefore, it is fundamental the use of alloys made up of metals with a low degree of ionic [10].

Titanium properties make it ideal for use in dental implants, and it has been used successfully in dentistry for many years [4]. Its high resistance to corrosion results from the formation of a thin highly-adhesive layer of titanium oxide, being at the same time extremely biocompatible. However, one of the main problems of using titanium in the manufacturing of prosthetic structures results from the difficulty in handling it during the casting process.

According to the A.D.A. (American Dental Association) [11] classification system, noble alloys consist of at least 25% gold or metals of the platinum group.

Precious alloys (of high gold, silver, palladium and platinum content) are usually implemented as bases for fixed metal-ceramic prostheses. Compared to titanium or stainless steel alloys, precious alloys are distinguished by a high corrosion resistance (significantly increased when containing more than 75% gold [12]) as well as a low-to-moderate mechanical resistance.

Due to their low electrochemical stability, non-noble alloys or base metal alloys (Cr-Ni) combined with c.p. titanium, show a high corrosion level. Therefore, their implementation is contraindicated in the manufacturing of prosthetic suprastructures over implants. In an in vitro study of corrosion on alloys that are in contact with titanium [3], it was observed that those alloys based on non–noble metals (Cr-Co, Cr-Ni) present a higher dissolution rate than alloys based on noble metals (Au, Pd).

Argen® Corporation developed Noble Bond® alloy, which is made up of 75% base metals and 25% ruthenium, the latter also belonging to the group of noble metals (Noble Bond® Alloy -Composition: Ruthenium 25%, Cobalt 40%, Chrome 24%, Gallium 11%, Boron lines).

The purpose of producing this alloy is to improve the base metals alloys (Cr-Co) resistance to corrosion and, at the same time, to offer a low cost material with electrochemical characteristics similar to those of the noble alloys.

The success of noble alloys with high content of gold, palladium and c.p. titanium in the production of prosthetic structures over implant–supported suprastructure [3, 13, 14] is well known because of both their biocompatibility and their resistance to corrosion. These are the reasons that led to a comparative analysis regarding the effects of electrolytic corrosion on two types of noble alloys: Argelite 76sf+® (Argen®) and Noble Bond® (Argen®) and c.p. titanium.

The main purpose of this study was to determine if the Noble Bond® alloy is an electrochemically suitable material to make prosthetic suprastructures over c.p. titanium implants.

Besides, the following aspects were analysed:

  • Degree of electrolytic corrosion caused by the Noble Bond® alloy in combination with c.p. titanium;
  • Degree of electrolytic corrosion caused by an alloy with high content of gold in combination with c.p. titanium;
  • Degree of electrolytic corrosion caused by c.p. titanium over implants and abutment.
  • A comparison of the results obtained for the three metals / alloys used in the implant-supported suprastructure.


In this prospective experimental study 15 ad modum transmucosal abutments (UCLA type) of 4.1 mm diameter coupled with 15 implants made of IV–degree titanium of 4 mm diameter and 10 mm length were used (B&W® Buenos Aires, Argentina).

Five out of the 15 abutments were castings that used Noble Bond® alloy (Trial Group 1 = TG 1); other five were castings that used Argelite 76sf+® noble alloy (Composition: Gold 1.8%, Palladium 75.7%, Ruthenium below 1%, Indium 8%, Gallium 6.3%, Tin below 1%, Copper 7.5%, Borium below 1%) (Trial Group 2 = TG 2); and the remaining five were abutments made in c.p. titanium (B&W® Buenos Aires, Argentina) (Control Group = CG).

Sample Preparation and Casting

All the cast samples were prepared from castable plastic cylinder abutments and for the c.p. titanium samples machined straight abutments (B&W® Buenos Aires, Argentina) were used.

The device used was a compact benchtop vacuum pressure casting machine with integrated power cooling and touch display Nautilus T from BEGO with Lolipot crucibles (Bremen, Germany). To avoid oxidation processes, casting was performed in new crucibles by induction in controlled atmosphere, following the specifications provided by each of the alloys’ manufacturers. Once the UCLA abutments were cast, they were sand-blasted with non-recycled aluminium oxide- particle size 50 microns- at 60 psi, in order to remove oxide and lining remains.

Sample polishing was carried out with diamond rubber points and polishing paste following one direction and according to the manufacturer’s specifications for both alloys. Finally, samples were decontaminated by immersion in distilled water and in ultrasonic cleaner for 10 minutes, procedure recommended by the manufacturers to remove polishing remains.

Fixation of prosthetic components on implants was carried out using c.p. titanium screws (B&W® Buenos Aires, Argentina) torqued at 35 N. Once the samples were obtained, they were placed in plastic containers and labeled (Fig. 1).

Fig. (1). Abutments cast on implants: 1. Noble Bond®-Titanium, 2. Argelite® Titanium, 3. Titanium-Titanium.

Sample Analysis and Treatment

Each sample was analysed using a confocal microscope (OLYMPUS®LEXT OLS4000 3D Laser Measuring Microscope), designed to obtain nanometric images, 3D measurements and to measure roughness levels. The images obtained correspond to three different zones analysed (Fig. 2):

  1. Abutment Neck (U Neck).
  2. Implant Neck (I Neck).
  3. Implant Body (I Body).
Fig. (2). The three different zones analysed in the samples.

The following 3D metric parameters were obtained in each of the photographed areas:

  • Sa:  Arithmetical mean height of the surface.
  • Sp:  Maximum height of peaks.
  • Sv:  Maximum height of valleys.

After labeled, samples were placed in plastic containers and immersed in modified Ericsson solution as artificial saliva whose behaviour is quite similar to that of natural saliva and is generally used in electrolytic corrosion studies (composition: NaCl= 0.600 / KCl = 0.720 / CaCl2.2H2O = 0.220 / KH2PO4 = 0.680 / Na2HPO4.12H2O = 0.856 / KSCN = 0.060 / KHCO3 = 1.500 / Citric acid = 0.030) [15].

Samples were kept immersed in the containers for three months, at the end of which, samples were analysed again using the same procedures applied at the beginning of the study (Fig. 3). The electrolyte was not changed during exposure.

Fig. (3). Samples immersed in modified Ericsson solution and their storage.

An analytical technique by static immersion with an increased immersion time [12, 15] and in accordance with ISO/ TR 10271:1993 was the methodology used for sample treatment.

Statistical Analysis

Parametric data obtained (Sa, Sp and Sv) in all samples, before and after immersing them in artificial saliva, were subjected to statistical treatment by running an ANOVA, LSD Fisher Alfa Test, and Tukey’s Alfa Test.


The tables below show the metric parameters obtained through the images of the samples studied, before and after artificial saliva immersion (Tables 1-6).

Table 1.
Data obtained from the Titanium-Titanium group before immersion in artificial saliva.
Sample Sector Sa Sp Sv
1 Abutment Neck (U Neck) 0.079 1.788 4.428
Implant Neck (I Neck) 0.098 1.299 1.546
Implant Body (I Body) 0.384 7.887 7.07
2 Abutment Neck (U Neck) 0.043 1.507 0.988
Implant Neck (I Neck) 0.059 0.903 0.872
Implant Body (I Body) 0.478 6.787 6.649
3 Abutment Neck (U Neck) 0.046 6.295 2.024
Implant Neck (I Neck) 0.09 3.028 2.045
Implant Body (I Body) 0.446 5.801 12.234
4 Abutment Neck (U Neck) 0.042 2.461 2.813
Implant Neck (I Neck) 0.196 2.775 4.318
Implant Body (I Body) 0.458 6.974 9.166
5 Abutment Neck (U Neck) 0.062 3.712 4.258
Implant Neck (I Neck) 0.06 1.862 1.18
Implant Body (I Body) 0.587 8.533 11.863
Table 2.
Data obtained from the Titanium-Argelite® group before immersion in artificial saliva.
Sample Sector Sa Sp Sv
6 Abutment Neck (U Neck) 0.039 1.955 0.809
Implant Neck (I Neck) 0.172 5.266 3.567
Implant Body (I Body) 0.345 8.564 14.786
7 Abutment Neck (U Neck) 0.042 4.226 1.565
Implant Neck (I Neck) 0.11 3.12 3.222
Implant Body (I Body) 0.361 14.215 12.9
8 Abutment Neck (U Neck) 0.038 3.178 1.883
Implant Neck (I Neck) 0.157 2.879 2.921
Implant Body (I Body) 0.542 12.845 13.927
9 Abutment Neck (U Neck) 0.229 4.729 3.563
Implant Neck (I Neck) 0.179 2.468 2.042
Implant Body (I Body) 0.394 19.706 15.759
10 Abutment Neck (U Neck) 0.392 8.676 6.768
Implant Neck (I Neck) 0.217 7.422 5.841
Implant Body (I Body) 0.538 9.46 12.604
Table 3.
Data obtained from the Titanium-Noble Bond® group before immersion in artificial saliva.
Sample Sector Sa Sp Sv
11 Abutment Neck (U Neck) 0.071 6.126 16.417
Implant Neck (I Neck) 0.114 1.998 1.892
Implant Body (I Body) 0.459 8.046 11.115
12 Abutment Neck (U Neck) 0.068 3.795 1.675
Implant Neck (I Neck) 0.157 2.231 3.305
Implant Body (I Body) 0.54 8.858 9.216
13 Abutment Neck (U Neck) 0.057 1.283 3.266
Implant Neck (I Neck) 0.112 2.097 2.564
Implant Body (I Body) 0.512 7.298 7.57
14 Abutment Neck (U Neck) 0.072 13.389 4.293
Implant Neck (I Neck) 0.117 3.959 5.794
Implant Body (I Body) 0.575 16.041 16.991
15 Abutment Neck (U Neck) 0.046 2.328 2.235
Implant Neck (I Neck) 0.118 2.013 2.486
Implant Body (I Body) 0.556 7.962 9.815
Table 4.
Data obtained from the Titanium-Titanium group after immersion in artificial saliva.
Sample Sector Sa Sp Sv
1 Abutment neck (U neck) 0.075 1.48 1.178
Implant neck (I neck) 0.071 2.141 3.927
Implant body (I body) 0.342 4.836 10.087
2 Abutment neck (I neck) 0.048 2.04 1.23
Implant neck (U neck) 0.062 2.774 4.923
Implant body (I body) 0.504 14.755 14.682
3 Abutment neck (U neck) 0.046 1.097 6.274
Implant neck (I neck) 0.051 2.512 0.93
Implant body (I body) 0.486 10.274 10.177
4 Abutment neck (U neck) 0.046 1.527 0.858
Implant neck (I neck) 0.092 1.837 1.326
Implant body (I body) 0.476 10.758 13.079
5 Abutment neck (U neck) 0.058 1.251 1.282
Implant neck (I neck) 0.06 0.907 0.997
Implant body (I body) 0.565 6.804 12.324
Table 5.
Data obtained from the Titanium-Argelite® group after immersion in artificial saliva.
Sample Sector Sa Sp Sv
6 Abutment neck (U neck) 0.051 1.535 1.454
Implant neck (I neck) 0.171 3.706 3.366
Implant body (I body) 0.432 5.802 15.634
7 Abutment neck (I neck) 0.046 1.938 1.913
Implant neck (U neck) 0.119 4.068 4.883
Implant body (I body) 0.48 7.681 10.358
8 Abutment neck (U neck) 0.035 3.261 2.863
Implant neck (I neck) 0.15 2.949 2.387
Implant body (I body) 0.635 6.566 16.501
9 Abutment neck (U neck) 0.034 3.389 1.469
Implant neck (I neck) 0.186 3.955 4.319
Implant body (I body) 0.621 7.662 23.614
10 Abutment neck (U neck) 0.036 2.359 2.52
Implant neck (I neck) 0.158 4.507 3.914
Implant body (I body) 0.621 15.512 17.969
Table 6.
Data obtained from the Titanium- Noble Bond® group after immersion in artificial saliva.
Sample Sector Sa Sp Sv
11 Abutment neck (U neck) 0.068 0.739 1.001
Implant neck (I neck) 0.116 4.692 2.518
Implant body (I body) 0.558 7.161 12.144
12 Abutment neck (I neck) 0.084 7.859 2.979
Implant neck (U neck) 0.152 3.847 4.119
Implant body (I body) 0.398 8.454 16.652
13 Abutment neck (U neck) 0.083 3.338 3.905
Implant neck (I neck) 0.126 3.379 4.021
Implant body (I body) 0.64 8.798 10.924
14 Abutment neck (U neck) 0.043 0.933 4.239
Implant neck (I neck) 0.096 2.216 2.862
Implant body (I body) 0.513 8.797 8.22
15 Abutment neck (U neck) 0.05 1.949 0.69
Implant neck (I neck) 0.129 2.905 2.261
Implant body (I body) 0.546 8.558 13.799

Sa; Arithmetical Mean Height of the Surface

Although in the abutment neck (U Neck) Argelite® alloy showed a decrease of the Sa after saliva immersion, this variation was not significant. No statistically significant differences were found for the other two alloys Sa values at this level. The analysis of the Sa at the level of the implant neck (I Neck) showed no statistically significant differences on its surface in combination with the three studied alloys.

Similar results were found for the surface of the implant body (I Body) in contact with the three studied alloys, even though a slight increase of the Sa in the Argelite® noble alloy was observed, differences were not statistically significant (Fig. 4).

Fig. (4). Sa variation at the three levels measured, before and after samples immersion in artificial saliva.

Sp, Maximun Height of Peaks

As for Sp values in the implant neck (I Neck), although there was a decrease in values, the observed changes in the three samples, before and after immersion in artificial saliva, were not significant at the statistical level.

In the implant neck (I Neck) Sp values remained much the same.

As for Sp values in the implant body (I Body), an increase of this value was observed in the c.p. titanium alloy and a decrease of this same value in the Argelite® one; however, the differences found were not statistically relevant. In the case of Noble Bond®, no statistically significant differences were found (Fig. 5).

Fig. (5). Sp variation at the three levels measured, before and after samples immersion in artificial saliva.

Sv, Maximun Height of Valleys

In the abutment neck (U Neck), a slight decrease in the Sv values in the Noble Bond® alloy was observed, but it was not statistically significant. No significant differences were found in the Argelite® alloy or in c.p. titanium.

Comparing the results before and after artificial saliva immersion, no differences were observed at the level of the implant neck (I Neck) in any of the three alloys. Comparing results in the implant body (I Body) area, a slight increase in the Argelite® alloy values was observed after immersion, but neither this increase nor the values obtained with the other two alloys were statistically significant (Fig. 6).

Fig. (6). Sv variation at the three levels measured, before and after samples immersion in artificial saliva.

An example of pre and post submersion of the samples is shown in Fig. (7)

Fig. (7). Pre and post sumersion image of one sample at the tree points observed.


All metals used in devices for biomedical prostheses degrade to a greater or lesser extent [4]. The purpose of this study was to determine if Noble Bond® alloy was a biomaterial electrochemically suitable to manufacture prosthetic suprastructures over c.p. titanium implants.

Adding a noble metal to non–noble alloys has already been done by Argen® company in Noble Crown NF® (Co-Pd-Cr-A) alloy and Noble Crown® (Ni-Pd-Cr) alloy. Although these alloys showed an increase in their nobility, they worsened the resistance to corrosion in comparison to the conventional Co-Cr and Ni-Cr–base alloys from an in vitro study performed by Sarantopoulos et al. [7]. Unlike these results, in the present study and after immersion in artificial saliva for three months, there were no signs of corrosion at the alloy’s surface level when ruthenium instead of palladium was used.

Regarding titanium abutments and titanium implants combined with the different alloys, no statically differences were observed between values obtained before and after immersing the samples in artificial saliva. This behaviour coincides with the one reported by other authors. Meffert et al. and Botha et al. concluded that initial rust gives titanium high resistance to corrosion, making it inert to tissues, and its low density provides it with a high resistance / weight relation making it highly biocompatible [16, 17].

Using titanium alloys to manufacture prosthetic suprastructures over implants avoids the problem of galvanic corrosion. A study carried out by Arismendi et al. [3] suggests that the best combination restoration–implant for trial conditions can be achieved by using c.p. titanium and a titanium alloy. Besides, titanium is considered one of the most corrosion-resistant materials used for biomedical purposes [5, 16, 18]. Two characteristics of titanium make it ideal for dental implants: its high mechanical resistance and its spontaneous passivation when in contact with water, air or tissue fluids [11].

The stable behaviour observed in noble alloys coincides with the results obtained in studies performed by other authors who concluded that noble alloys with high content of gold and palladium combined with c.p. titanium implants present high resistance to corrosion with minimum release of the metal’s ions to the medium, as they develop a passivation mechanism when in contact with the medium [3, 5, 14]. Palladium-based alloys without silver show a rather passive behaviour and better than the Pd-Ag alloys [12]. Similarly, Cortada [9], in a galvanic corrosion study, concluded that palladium–based alloys present low levels of ions release in combination with titanium. In addition, it was shown that resistance to corrosion in silver–palladium based alloys is compatible with alloys with high contents of gold studied in artificial saliva [3, 5, 14]. In the present study there was no significant surface modification (Sa, Sp, and Sv) of the samples at U neck, I neck or I body when Argelite® alloy was used.

The methodology applied to treat the samples consists in an analytical technique through static immersion under ISO/TR 10271:1993 standards. The only variation introduced was an increase in the period of samples immersion [12, 19]. Further in vitro studies with longer periods of samples immersion in artificial saliva and in vivo studies are recommended.


No statistically significant differences between experimental Noble Bond® alloy, noble alloy and c.p. titanium alloys were found in the present study as regards electrogalvanic corrosion, measured through tridimensional changes that took place on the surface of the samples (Sa, Sp, and Sv) three months after having been immersed in artificial saliva, both at abutment level or at implant neck and body levels. Further research on longer periods of immersion is necessary to validate these preliminary results.


The authors confirm that this article content has no conflict of interest.


The authors thank Luis Croharé (ABO, Faculty of Dentistry, National University of Cordoba) for cooperation related to the statistical analysis of the data in this study.


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