Elsevier

Dental Materials

Volume 31, Issue 11, November 2015, Pages 1370-1376
Dental Materials

The effect of aqueous media on the mechanical properties of fluorapatite–mullite glass–ceramics

https://doi.org/10.1016/j.dental.2015.08.152Get rights and content

Abstract

Objectives

To verify the effects of alternating thermal changes in aqueous media and chemical composition on mechanical properties of apatite–mullite glass–ceramics and to investigate concentration of ions eluted from glass–ceramics in aqueous media.

Materials and methods

The glass compositions were from SiO2single bondAl2O3single bondP2O5single bondCaOsingle bondTiO2single bondBaOsingle bondZrO2single bondCaF2 system. Glass–ceramics were prepared by heat-treating at 1100 °C for 3 h samples alternately immersed in water at 5 and 60 °C. The 3-point bending strength (n = 10) were determined using 3 × 4 × 25 mm/bar and a universal testing machine, at a cross-head speed of 0.1 mm/min. Vickers micro hardness were evaluated by applying a total of 15–20 indentations under a 100 g load for 30 s. Concentrations of ions eluted from glass–ceramics immersed in 60 ± 5 °C double distilled water were determined by ion chromatography. The toxicity of glass–ceramics was assessed by seeding the osteosarcoma cells (MG63) on powder for different days and their cell proliferation assessment was investigated by MTT assay. The data were analyzed using one way analysis of variance and the means were compared by Tukey's test (5% significance level).

Results

The highest flexural strength and hardness values after thermal changes belonged to TiO2 and ZrO2 containing glass–ceramics which contained lower amount of released ions. BaO containing glass–ceramic and sample with extra amount of silica showed the highest amount of reduction in their mechanical strength values. These additives enhanced the concentration of eluted ions in aqueous media. MTT results showed that glass–ceramics were almost equivalent concerning their in-vitro biological behavior.

Significance

Thermal changes and chemical compositions had significant effects on flexural strength and Vickers micro-hardness values.

Introduction

The growing trend for dental restorative materials has pushed on to the development of novel glass–ceramic systems [1], [2], [3]. Glass–ceramics are composed of one or more crystalline phases which are surrounded by a glassy matrix. Heat-treatment process of the base glass which contains controlled crystallization and growth steps is one of the conventional methods in preparation and manufacturing of glass–ceramics [4]. These materials have advantages over other bioceramics since their mechanical and biological properties are easily adjustable by using different amount of additives [3], [4], [5]. The anti-bacterial effect of F ions and the presence of needle-like fluorapatite crystals in natural bone and teeth make fluorapatite containing glass–ceramics promising candidates for medical and dental applications [6], [7], [8], [9]. Glass–ceramics based on interlocking microstructures of apatite and mullite crystals have previously been developed for dental restorations [10], [11], [12], [13], [14]. These glass–ceramics contain dispersed fluorapatite (Ca10(PO4)6F2) and mullite crystals (3Al2O3·2SiO2) in a glassy matrix [10], [11], [12], [13], [14]. Small crystals of fluorapatite, in these materials, result in biocompatibility and very special optical properties such as translucency and opalescence whilst mullite crystals induce adequate mechanical properties [11], [13]. Microstructure and chemical characteristic of glass–ceramic materials, chemical nature and temperature of the surrounding environment and duration of exposure to this environment are some factors which can manipulate the mechanical performance and chemical durability of dental glass–ceramics [15], [16], [17]. Rapid and cyclic thermal changes in the oral cavity, which can exert considerable thermal stresses on the restorations solely or in the presence of the applied load of chewing process, are some of the other crucial issues which have unfavorable effects on mechanical properties of these materials [16], [17], [18], [19]. These thermal stresses can be simulated by thermo-cycling process which is based on alternating temperature changes in aqueous media [18]. In a separate study, we focused on the performance of minor glass ingredients such as TiO2, ZrO2, BaO and additional amount of silica in points of crystallization behavior, microstructure and mechanical properties of an apatite–mullite based glass–ceramic system [20]. Our results showed that small amounts of the above mentioned additives changed the microstructure and mechanical properties of the base glass–ceramic system in different ways [20]. Despite the numerous studies about the effect of aqueous and acidic media on mechanical properties of silicate glasses, to our knowledge few studies have investigated the effect of alternative thermal changes on flexural strength and hardness variations in dental glass–ceramics [17], [18], [19]. Such information is of practical importance to manufacture and application of apatite–mullite glass–ceramics in dentistry and other biomedical applications and can lead to better prediction of the future clinical behaviors of these materials [17], [18], [19]. Therefore, the objective of this study is to verify the effect of thermo-cycling process duration on the strength and microhardness properties of the apatite–mullite glass–ceramics, concerning their different microstructures and chemical compositions.

Section snippets

Specimen preparation

The raw materials used to produce the glass–ceramic samples are shown in Table 1. 5 groups of glass–ceramics coded as G, GS, GZ, GB and GT with the batch formulations shown in Table 2 were prepared according to the procedure completely described in [20]. Briefly, thoroughly mixed batches were melted at 1550 °C for 2 h. The resulted molten glasses were cast into a pre-heated steel mold and were cooled naturally to room temperature. Flexural strength and micro-hardness samples were prepared by

Mechanical properties

Table 3 depicts the flexural strength of glass–ceramic samples at specified number of thermal-cycles. As indicated in this table, flexural strength values declined with different rates after thermal process. The number of cycles at which mechanical strength of different glass–ceramic compositions experienced first significant decline and the amount of ultimate loss were two crucial factors which were distinctive in prepared glass–ceramic compositions. The results of Table 3 indicated that

Discussions

The rapid decline in flexural strength values of G, GS and GZ glass–ceramic compositions at the initial stages of the thermo-cycling process can be partly attributed to higher amounts of residual glassy phase in these samples [14], [20]. Previously reported DTA results [20] indicated that higher viscosity of the aforementioned glasses led to the crystallization at relatively higher temperatures. Late onset of crystallization in these glasses resulted in higher amounts of residual glassy phase

Conclusion

Flexural strength and hardness values of apatite–mullite glass–ceramic samples including distinctive amounts of TiO2, ZrO2, BaO and extra amounts of SiO2 changed differently after thermo-cycling process. While after thermal changes, mechanical properties values remained almost un-changed in glass–ceramic samples containing small amounts of TiO2 and ZrO2, these values experienced the highest amounts of reduction with the addition of BaO and extra amounts of SiO2. After immersion in hot water,

Acknowledgements

This study was supported by research grant number ‘12846-69-01-90’ from Tehran University of Medical Science, Faculty of Dentistry. The authors would also like to thank Dr. Mohammad J. Kharazi Fard consulting assistant at Tehran University of Medical Science, Faculty of Dentistry, for helpful inputs

References (33)

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