Arzu Tezvergil

The effect of fiber orientation on the thermal expansion coefficients of fiber-reinforced composites

OBJECTIVES The aim of this study was to characterize the thermal expansion and dimensional changes of fiber-reinforced composite (FRC) according to the fiber orientation, brand of FRC product and polymerization conditions. METHODS Cubic specimens (n=5) were prepared from different brands of FRC and particulate filler composites and dimethacrylate monomer resin. The specimens were polymerized with a light-curing device for 40 s or additionally with prolonged polymerization in the light-curing oven for 15 min. Linear coefficients of thermal expansion (LCTE) values for different materials and for FRC with different fiber orientations were determined using a thermomechanical analyzer. RESULTS All specimens exhibited linear increase in the value of LCTE between 37 and 67 degrees C. The analysis of ANOVA revealed that orientation of fiber and brand of material had significant effect (P<0.001) on LCTE values for 37-67 degrees C interval. Some interaction between factors also existed. Also, temperature interval 110-150 degrees C had significant effect on the LCTE values according to the curing unit, brand and orientation of fibers. SIGNIFICANCE The results of this study suggest that the anisotropic nature of FRC exists also with regard to thermal expansion. The variation of LCTE of FRC compared to that of particulate filler composites might influence the interfacial adhesion of FRC appliances.

The effect of length and concentration of glass fibers on the mechanical properties of an injection- and a compression-molded denture base polymer

STATEMENT OF PROBLEM Fiber-reinforcement has been used to overcome the mechanical limitations of denture base polymers. One major difficulty in the use of fiber reinforcement has been the addition of fibers during conventional processing methods. PURPOSE This study evaluated the effect of various lengths and concentrations of chopped E-glass fiber-reinforcement on the transverse strength, modulus of elasticity, and impact strength of injection and compression-molded polymethyl methacrylate based denture base polymer. MATERIALS AND METHODS Test specimens (n=10) of 4-, 6-, and 8-mm fiber length and 1%, 3%, and 5% weight fiber concentrations were prepared with either an injection or a compression-molded processing method. Denture base polymer specimens without any fiber reinforcement were used as control for both processing methods. Transverse strength test specimens (65 x 10 x 2.5 mm) were stored in water bath at 37 degrees C for 2 weeks. The transverse strength (MPa) and modulus of elasticity (GPa) was measured with the 3-point bending test. Impact strength (kJ/m(2)) test specimens (60 x 7.5 x 4 mm) were tested with the Charpy-type pendulum impact test setup. The data were analyzed with multifactorial analysis of variance and Tukey post hoc tests (alpha=.05). RESULTS Injection-molded fiber-reinforced groups showed significantly higher transversal strength, elastic modulus, and impact strength compared with compression-molded groups (P <.001). In the injection-molded groups, fiber concentration increased all mechanical properties tested (P <.05), but fiber length only increased transverse strength and modulus of elasticity (P <.05). In the compression molded groups, fiber concentration affected modulus of elasticity and impact strength significantly (P <.05), but fiber length did not show any significant effect on the mechanical properties tested (P >.05). CONCLUSION The transverse strength, elastic modulus and impact strength of injection-molded denture base polymer increased significantly with the use of chopped E-glass fibers, whereas the effect was not significant with the compression-molded polymer.

Acoustic emission analysis of fiber-reinforced composite in flexural testing.

OBJECTIVES The aim of this study was to examine the emission of acoustic signals from six commercially available fiber-reinforced composites (FRC) used in the frameworks of fixed partial dentures in material bending. METHODS FRC test specimens were made of six commercially available fiber products of polyethylene or glass and five light-curing resins. FRC test specimens were polymerized with a hand light-curing unit or with a light-curing oven. The flexural test for determination of ultimate flexural strength of test specimens (n = 6) was based on the ISO 10477 standard after the specimens were stored in air or in water for two weeks. The acoustic emission (AE) signals were monitored during three-point loading test of the test specimens using a test with increasing loading levels until the specimens fractured. RESULTS Generally, stress level required for the AE activity initiation ranged from 107 MPa (Ribbond) to 579 MPa (everStick). The ultimate flexural strength of FRC specimens were higher, ranging from 132 to 764 MPa, being highest with everStick and Vectris FRC, and lowest with Ribbond FRC. ANOVA showed a statistically significant difference between the initiation of AE activity and the ultimate flexural strength according to the brand (p < 0.001) storing conditions (p < 0.001) and polymerization procedure (p < 0.001). AE activity and ultimate flexural strength correlated significantly (p < 0.010, r = 0.887). SIGNIFICANCE The result of this study suggested that AE activity in FRC specimens started at a 19-32% lower stress level than occurred at final fracture.

Evaluation of some properties of two fiber-reinforced composite materials

Objective. Water sorption, flexural properties, bonding properties, and elemental composition of photopolymerizable resin-impregnated fiber-reinforced composite (FRC) materials (everStick C&B and BR-100) (FPD) were evaluated in this study. Material and methods. Bar-shaped specimens (2×2×25 mm) were prepared for water sorption and flexural strength testing. The specimens (n=6) were polymerized either with a hand light-curing unit for 40 s or, additionally, in a light-curing oven for 20 min and stored in water for 30 days. Water sorption was measured during this time, followed by measurements of flexural strength and modulus. A shear bond strength test was performed to determine the bonding characteristics of polymerized FRC to composite resin luting cement (Panavia-F), (n=15). The cement was bonded to the FRC substrate and the specimens were thermocycled 5000 times (5–55°C) in water. SEM/EDS were analyzed to evaluate the elemental composition of the glass fibers and the fiber distribution in cross section. Results. ANOVA showed significant differences in water sorption according to brand (p<0.05). Water sorption of everStick C&B was 1.86 wt% (hand-unit polymerized) and 1.94 wt% (oven polymerized), whereas BR-100 was 1.07 wt% and 1.17 wt%, respectively. The flexural strength of everStick C&B after 30 days’ water storage was 559 MPa (hand-unit polymerized) and 796 MPa (oven-polymerized); for BR-100, the values were 547 MPa and 689 MPa, respectively. Mean shear bond strength of composite resin cement to the FRC varied between 20.1 and 23.7 MPa, showing no statistical difference between the materials. SEM/EDS analysis revealed that fibers of both FRC materials consist of the same oxides (SiO2, CaO, and Al2O3) in ratios. The distribution of fibers in the cross section of specimens was more evenly distributed in everStick C&B than in BR-100. Conclusion. The results of this study suggest that there are some differences in the tested properties of the FRC materials.

Repair bond strength of restorative resin composite applied to fiber‐reinforced composite substrate

Delamination or fracture of composite veneers can occur as a result of improper design of the fiber‐reinforced composite (FRC) framework. This in vitro study tested the repair bond strength of restorative composite to aged FRC. The substrate was multiphase polymer matrix FRC (everStick) aged by boiling for 8 h and storing at 37°C in water for 6 weeks. The aged substrate surfaces were wet‐ground flat with 1200‐grit silicon carbide paper and subjected randomly to 5 different surface treatments: 1) An adhesion primer (Composite Activator) and resin (CA), 2) Silane (EspeSil) and resin (SIL‐MP), 3) Silane, adhesive primer, and resin (Clearfil Repair) (CF), 4) Air particle‐abrading (CoJet), silane, and resin (CJ‐SIL‐MP), 5) Resin (Scotchbond Multipurpose Resin) only as control (MP). Restorative composite resin (Z250) was added to the substrate in 2 mm layer increments and light‐cured. Subsequently, every surface treatment group was divided into 2 subgroups of 12 specimens each. The specimens were either 48 h water‐stored or thermocycled (6000 x 5–55°C). The shear bond strengths of composite resin to FRC were measured at a crosshead speed of 1.0 mm/min. The data were analyzed by ANOVA for factors ‘treatment type’ and ‘storage condition’; Tukeys post‐hoc tests and Weibull analysis were performed. ANOVA showed a significant difference as a function of surface treatment (P<0.05) and storage condition (P<0.05). The CJ‐SIL‐MP group showed highest bond strength and Weibull modulus after thermocycling. Repair of multiphase polymer matrix FRC may show reliable bond strength when silane treatment is used along with air‐particle abrading.

Water Sorption, Solubility and Dimensional Changes of Denture Base Polymers Reinforced with Short Glass Fibers

The aim of this study was to determine water sorption, solubility and dimensional stability of injection and compression-molded polymethyl methacrylate based denture base polymer that was reinforced with various concentrations and lengths of E-glass fibers. For water sorption and solubility, 20 test groups with different fiber contents and lengths of fibers were prepared. Test specimens without fibers were used as a control. The water sorption and solubility was measured after 90 days water storage. For dimensional stability, rhombic test specimens were prepared and the dimensional changes were measured after processing, drying and storing in water for 4 days and 30 days and were compared with those on the brass model. The water sorption and solubility of injection-molded denture base polymer was lower compared to compression-molded specimens (p<0.05). The dimensional accuracy of denture base polymer was not affected with fiber reinforcement (p>0.05).

Comparison between regional micropush-out and microtensile bond strength of resin composite to dentin.

Objective. In this study we compared the micropush-out (µ-PO) and microtensile (µ-TBS) test methods for resin composites on different levels and surfaces of dentin. Material and Methods. Thirty-four sound human molars were divided into two groups in accordance with the dentin surface used (occlusal (O) or mesio-distal (M)), then subdivided into a further two groups in accordance with the test method (µ-PO (P) or µ-TBS (T)). In groups OP and OT, teeth were ground occlusally perpendicular to their axis, and in groups MP and MT, mesio-distally parallel to their axis to expose dentin. Dentin disks were prepared from different regions of the teeth either in an occluso-cervical (group OP) (n=5) or mesio-distal direction (group MP) (n=5) (S, superficial; M, middle; D, deep). One-hundred-and-twenty standardized occlusal cavities were prepared in these dentin disks using a conical-shaped diamond rotary cutting instrument. The adhesive (Adper Scotchbond Multi-Purpose Dental Adhesive) and a composite material (Filtek Z250 Universal Restorative) were applied and polymerized with a LED light curing unit (Elipar FreeLight 2). The disks (n=20/per group) were tested in a universal testing machine and pushed out with a cross-head speed of 1.0 mm/min. In groups OT (n=12) and MT (n=12), the teeth were ground to expose superficial, middle, and deep dentin. Build-ups of resin composite were constructed with the same materials. The specimens were serially sectioned and trimmed to hour-glass shapes, then tested with the µ-TBS tester at a rate of 1 mm/min. Failure modes were examined using a stereomicroscope and scanning electron microscope. Results. ANOVA revealed significant differences among the groups (p<0.001). With the push-out test, no premature failure occurred, the variability of the data distribution was acceptable, and regional differences in bond strength among dentin levels could be assessed. Conclusions. The µ-PO test method could be an alternative to the µ-TBS technique.

In vitro repair of fractured fiber-reinforced cusp-replacing composite restorations.

Objective. To assess fracture resistance and failure mode of repaired fiber-reinforced composite (FRC) cusp-replacing restorations. Methods. Sixteen extracted human premolars with fractured cusp-replacing woven (Group (A)) or unidirectional (Group (B)) FRC restorations from a previous loading experiment were repaired with resin composite and loaded to fracture. Results. Differences in fracture loads between groups were not statistically significant (P = 0.34). Fracture loads of repaired specimens were significantly lower than those of original specimens (P = 0.02 for Group (A) and P < 0.001 for Group (B)). Majority of specimens showed failure along the repaired surface. In Group (B) 89% of specimens showed intact tooth substrate after restoration fracture, while this was 28% in Group (A) (P = 0.04). Conclusion. Fractured cusp-replacing FRC restorations that are repaired with resin composite show about half of fracture resistance of original restorations. Mode of failure with a base of unidirectional fibers is predominantly adhesive.