F.s. Sayyedan, M.h. Fathi, H. Edris, A. Doostmohamadi, V.s., Mortazavi, F. Shirani,
Volume 33, Issue 3 (3-2015)
Abstract
The objective of this study was to synthesize glass ionomer–forsterite nanocomposite and study the effect of
incorporating forsterite nanoparticles to the ceramic part of glass ionomer cement in order to improve mechanical properties and
bioactivity. So, Forsterite nanoparticles were made by the sol-gel process using different weight percentages added to the ceramic
part of commercial GIC (Fuji II GC). X-ray diffraction (XRD) was used in order to characterize and determine grain size of the
produced forsterite nanopowder. In order to study the mechanical properties of the produced glass ionomer cement-forsterite
nanocomposite, the compressive strength (CS), three-point flexural strength (FS) and diametral tensile strength (DTS) of
specimens were measured. Statistical analysis was done by one Way ANOVA and differences were considered significant if
P‹0.05. The morphology of fracture surface of specimens was studied using scanning electron microscopy (SEM) technique.
Bioactivity of specimens was investigated by Fourier transitioned-infrared spectroscopy (FTIR), scanning electron microscopy
(SEM), and Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES). The results of XRD analysis confirmed the
nanocrystalline and pure forsterite synthesis. According to the mechanical properties measurements, the optimum weight
percentages of forsterite nanoparticles for enhancement of CS, FS, and DTS were obtained equal to 3, 1 and 1 wt.%, respectively.
Statistical analysis showed that the differences between all the groups were significant (P<0.05). SEM images and results of the
ICP-OES and FTIR tests confirmed the bioactivity of the nanocomposite. Glass ionomer-forsterite nanocomposite containing 1 to
3 wt.%-forsterite nanoparticles can be a suitable candidate for dentistry and orthopedic applications due to the improvement of
mechanical properties and bioactivity.
M. Rezazadeh, M.r. Saeri, F. Tirgir Malkhlifeh, A. Doostmohammdi,
Volume 35, Issue 2 (9-2016)
Abstract
The aim of the present study is to study the effects of adding diopside (CaMgSi2O6) as well as silica sulfuric acid nanoparticles to ceramic part of glass ionomer cement (GIC) in order to improve its mechanical properties. To do this, firstly, diopside (DIO) nanoparticles with chemical formula of CaMgSi2O6 were synthesized using sol-gel process and then, the structural and morphological properties of synthesized diopside nanoparticles were investigated. The results of scanning electron microscopy (SEM) and particle size analyzing (PSA) confirmed that synthesized diopside are nanoparticles and agglomerated. Besides, the result of X-ray diffraction (XRD) analyses approved the purity of diopside nanoparticles compounds. Silica sulfuric acid (SSA) nanoparticles are also prepared by chemical modification of silica nanoparticles by means of chlorosulfonic acid. Fourier transform infrared spectroscopy (FTIR) technique was used to find about the presence of the (SO3H) groups on the surface of silica sulfuric acid nanoparticles. Furthermore, various amounts (0.1, 3 and 5 wt.%) of diopside and silica sulfuric acid nanoparticles were added to the ceramic part of GIC (Fuji II GIC commercial type) to produce glass ionomer cement nanocomposites. The mechanical properties of the produced nanocomposites were measured using the compressive strength, three-point flexural strength and diametral tensile strength methods. Fourier transform infrared spectroscopy technique confirmed the presence of the (SO3H) groups on the surface of silica nanoparticles. The compressive strength, three-point flexural strength and diametral tensile strength were 42.5, 15.4 and 6 MPa, respectively, without addition. Although adding 1% silica solfonic acid improved nanocomposite mchanical properties by almost 122%, but maximum increase in nanocomposite mechanical properties was observed in the nanocomposites with 3% diposid, in which 160% increase was seen in the mechanical properties.
