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Wear and Mechanical Properties of Nano-silica-fused Whisker CompositesPaffenbarger Research Center, American Dental Association Foundation, National Institute of Standards and Technology, Building 224, Room A-153, Stop 8546, Gaithersburg, MD 20899-8546, USA; Correspondence: * corresponding author, hockin.xu{at}nist.gov
Resin composites must be improved if they are to overcome the high failure rates in large stress-bearing posterior restorations. This study aimed to improve wear resistance via nano-silica-fused whiskers. It was hypothesized that nano-silica-fused whiskers would significantly improve composite mechanical properties and wear resistance. Nano-silicas were fused onto whiskers and incorporated into a resin at mass fractions of 0%-74%. Fracture toughness (mean ± SD; n = 6) was 2.92 ± 0.14 MPam for whisker composite with 74% fillers, higher than 1.13 ± 0.19 MPam for a prosthetic control, and 0.95 ± 0.11 MPam for an inlay/onlay control (Tukeys at 0.95). A whisker composite with 74% fillers had a wear depth of 77.7 ± 6.9 µm, less than 118.0 ± 23.8 µm of an inlay/onlay control, and 172.5 ± 15.4 µm of a prosthetic control (p < 0.05). Linear correlations were established between wear and hardness, modulus, strength, and toughness, with R = 0.95–0.97. Novel nano-silica-fused whisker composites possessed high toughness and wear resistance with smooth worn surfaces, and may be useful in large stress-bearing restorations.
Key Words: dental resin composite nano-silica-fused whiskers wear mechanical properties mechanisms
The performance of a dental composite depends on filler type, resin composition, filler-matrix bonding, and cure conditions (Wendt, 1987; Pallav et al., 1989; Ferracane et al., 1998; Watts and Hindi, 1999; Lim et al., 2002). Short fibers (Krause et al., 1989) and networked fibers (Ruddell et al., 2002) have been used to reinforce composites, resulting in modest strength increases. The degree of polymerization conversion has been increased via heat-treatment, leading to moderate strength increases (Loza-Herrero et al., 1998). Further improvements are needed for composites to overcome brittle fracture and high failure rates in large stress-bearing restorations (Tyas, 1990; Christensen, 1999; Donly et al., 1999), especially those that involve the replacement of tooth cusps. Recently, nano-silica-fused whiskers were incorporated into resins, resulting in strength increases (Xu, 2000; Xu et al., 2000). Silica was fused onto whiskers to enhance silanization and retention in the resin by roughening the whisker surfaces. Besides strength, occlusal wear resistance is also a major requirement for the longevity of restorations (Pallav et al., 1989; Bayne et al., 1992; Peutzfeldt and Asmussen, 1992; Wassell et al., 1994; Leinfelder and Suzuki, 1999; Manhart et al., 2000). Wear tests have been developed to simulate in vivo wear (Delong et al., 1985; Sakaguchi et al., 1986; Suzuki et al., 1996; Lim et al., 2002). Three-body wear with artificial food slurries produced data that corresponded well with clinical results (de Gee et al., 1996; Condon and Ferracane, 1997; Leinfelder and Suzuki, 1999; Xu et al., 1999). Filler levels, filler treatments, and degrees of cure have been shown to influence wear (Condon and Ferracane, 1997; Lim et al., 2002). Fine fillers have been used to reduce inter-particle spacing to improve wear resistance (Pallav et al., 1989; Bayne et al., 1992). The aim of this study was to investigate the effects of nano-silica-fused whisker filler level on composite wear, and to examine the relationships between wear and mechanical properties. It was hypothesized that increasing nano-silica-fused whisker fillers would increase the composite wear resistance, and that wear rate would decrease when composite mechanical properties (hardness, elastic modulus, flexural strength, and fracture toughness) were increased.
Specimen Fabrication Nano-silica (Degussa, Ridgefield, NJ, USA) having particles of 60 nm to 120 nm (mean = 80 nm) was used. Silicon nitride whiskers (UBE, New York, NY, USA), with diameters ranging from 0.1 µm to 2 µm (mean = 0.4 µm) and lengths from 2 µm to 30 µm (mean = 5 µm), were used. Whiskers were mixed with silica at a whisker:silica mass ratio = 2:1 by being stirred in ethyl alcohol on a hot plate until dry. The mixed powder was heated in a furnace at 800°C for 30 min to fuse the nano-silica onto the whiskers (Xu, 2000). The powder was silanized with mass fractions of 4% 3-methacryloxypropyltrimethoxysilane and 2% n-propylamine in cyclohexane in a rotary evaporator. The silanized powder was mixed with a resin monomer of mass fractions of 48.965% of an oligomeric urethane derivative of Bis-GMA (Caulk/Dentsply, Milford, DE, USA), 48.965% triethylene glycol dimethacrylate (TEGDMA), 2% benzoyl peroxide, and 0.07% 4-methoxylphenol. Filler mass fractions (%) of 0, 20, 40, 60, 70, and 74 were used following recommendations in previous studies (Xu, 2000; Xu et al., 2000). A previous study showed that composite with 70% and 74% fillers possessed high strengths, while the paste with 79% fillers was dry and the specimens had a lower strength (Xu, 2000). For fracture toughness, the paste was placed into steel molds of 2 x 2 x 25 mm3 and heat-cured at 120°C for 30 min for indirect applications, because the specimens were too opaque to be light-cured. For wear-testing, the paste was placed in molds of 4 mm diameter and 3 mm depth and cured in the same manner. An indirect inlay/onlay composite (Concept, Ivoclar, Amherst, NY, USA), referred to as inlay/onlay control, was cured in the Concept Heat-Integrated Processor at 120°C for 10 min under a pressure of 0.6 MPa. Concept consisted of 53–56% mass fraction of 40 nm silica and 20% radiopaque fillers, for a total of 73–76% in a urethanedimethacrylate resin. An indirect prosthetic composite (Artglass, Heraeus Kulzer GmbH, Wehrheim, Germany), referred to as prosthetic control, was cured in a Dentacolor-XS photo-curing unit for 90 sec. Artglass contained 70% barium-aluminum-silicate (mean particle size = 1 µm) in a resin with tetra- and hexa-functional groups and conventional bi-functional methacrylates.
Testing Wear specimens were tested in a four-station apparatus (Caulk/Dentsply, Milford, DE, USA) (Suzuki et al., 1996; Xu et al., 1999). Each specimen was surrounded by a brass ring filled with a water slurry, 63% of which was comprised of polymethyl methacrylate (PMMA) beads (mean particle size = 44 µm). A carbide steel pin with 3-mm tip diameter was loaded onto the specimen submerged in the PMMA slurry. The pin was pressed down against the PMMA particles on the specimen and rotated 30°. Upon reaching a maximum load of 76 N, the pin was counter-rotated during unloading and moved upward back to its original position. Each specimen was subjected to 400,000 wear cycles. Forty-eight specimens were tested for the 6 filler levels and 2 controls with 6 repeats. The sizes and depths of the wear scars were measured with the use of a computer-controlled profilometer (Mahr, Cincinnati, OH, USA) with a 5-µm diamond stylus. For each wear scar, profilometric tracings were made at intervals of 50 µm in 2 directions perpendicular to each other, with the unworn surface as baseline. The maximum values in the 2 perpendicular directions were averaged to yield the maximum depth and diameter for each wear scar (Xu et al., 1999).
The worn specimens were gold-coated and observed in a scanning electron microscope (SEM, JSM-5300, JEOL, Peabody, MA, USA). The data were analyzed by one-way ANOVA and Tukeys Multiple Comparison procedures (
Nano-sized silica particles were fused onto the whiskers at 800°C (Fig. 1A , significantly higher than those from 0% to 40%, 1.13 ± 0.19 MPam for the prosthetic control, and 0.95 ± 0.11 MPam for the inlay/onlay control (Tukeys at 0.95).
Wear scar depth, diameter, and volume decreased significantly (one-way ANOVA; p < 0.001) with increasing filler level (Fig. 2
We examined SEM micrographs of the worn surfaces inside the wear scars for unfilled resin and for whisker composites with 60% and 74% fillers (Figs. 3A
Increasing the nano-silica-fused whisker filler level improved the composite wear resistance. This is consistent with previous studies on wear and filler level (Bayne et al., 1992; Condon and Ferracane, 1997; Lim et al., 2002). The cracks in the wear scars of unfilled resin were also consistent with previous observations (Baran et al., 1998). Whisker composites with fillers from 20% to 74% had relatively smooth worn surfaces, free of cracks like those in unfilled resin. The transition from cracking to non-cracking likely occurred between filler levels of 0% and 20%. A similar transition from brittle behavior to a more tough behavior was observed in a previous study (Xu, 1999). The unfilled resin cracked more readily, creating a flat surface from fast fracture (Fig. 2B Comparison can also be made with dental amalgam, which is known for its resistance to occlusal wear and is taken as the standard by which newer restorative materials are judged. A previous study, in which the same operator used the same equipment, subjected amalgam (Dispersalloy, Dentsply, Milford, DE, USA) to 400,000 cycles of three-body wear, and measured a wear scar depth of 134 ± 54 µm and a diameter of 778 ± 270 µm (Xu et al., 1999). The whisker composite with 74% fillers had a wear scar depth of 77.7 ± 6.9 µm and a wear diameter of 742 ± 46 µm. Regarding the correlation between these in vitro wear values and clinical wear, a previous study reported on results with use of the same type of wear machine, compared with in vivo data (Leinfelder and Suzuki, 1999). These investigators found that the 400,000-cycle in vitro wear values agreed with the in vivo wear values over a three-year period. This is consistent with results from another study showing that a wear depth of 100–160 µm occurred for amalgam in 2–3 yrs (DeLong et al., 1985).
Wear of dental materials is a complex process involving fatigue, erosive, adhesive, abrasive, and corrosive components. Nevertheless, wear occurs via microfracture and material removal; hence it is inherently related to mechanical properties. McKinney et al.(1987) suggested that "wear does not necessarily vary in a manner consistent with the hardness." Pallav et al.(1989) found "the absence of a relationship between wear" and hardness or diametral tensile strength. Hardness of the nano-silica-fused whisker composites has been measured by nano-indentation (Xu et al., 2000). Contrary to previous reports, we found a good correlation between wear depth and hardness for whisker composites, with a correlation coefficient of R = 0.97 (Fig. 4A
Tyas (1990) found some correlation, but not significant correlation, between wear and elastic modulus. Peutzfeldt and Asmussen (1992) concluded that no correlation was established between wear and modulus of elasticity. For the whisker composites, with the wear depth measured here and elastic modulus from a previous study (Xu et al., 2000), a linear correlation was found between wear and elastic modulus, with R = 0.97 (Fig. 4B
A linear correlation between wear and flexural strength was found previously (Peutzfeldt and Asmussen, 1992). A similar relationship was found for whisker composites (Fig. 4C
Wear involves microfracture; hence, it is also expected to depend on fracture toughness (arrows in Figs. 3A
When the inlay/onlay and prosthetic controls were included in the fitting, the correlation coefficients between wear depth and hardness, elastic modulus, flexural strength, and fracture toughness fell to 0.86, 0.87, 0.74, and 0.78, respectively. This indicates that the resin composition and degree of cure may also have influenced wear. Further study should examine whether such relationships are unique to a single class of composites or can be generalized across classes of composites. The measured wear and mechanical properties depend on the measurement methods. For example, flexural strength may depend on the bending span and the loading rate. Therefore, while fundamental relationships may exist, one should not expect to produce relationships similar to those illustrated in Fig. 4 In conclusion, novel nano-silica-fused whisker composites were developed with in vitro wear resistance higher than that of conventional glass-particle-filled composites and similar to that of dental amalgam. The wear surfaces of whisker composites were smooth and free of cracks. Linear correlations were established between composite wear and hardness, elastic modulus, flexural strength, and fracture toughness. Nano-silica-fused whisker composites with superior strength, fracture toughness, and wear resistance are relatively opaque and may be useful in large stress-bearing posterior restorations involving cusps and indirect applications. Further studies should match the refractive index of whiskers to that of the resin to improve the esthetics for anterior applications.
The authors thank Dr. Frederick C. Eichmiller for discussions, and Dr. Joseph M. Antonucci for providing the resin monomer. This study was supported by NIDCR grant R29 DE12476 (Xu), by NIST, and by the ADAF.
DISCLAIMER Received for publication July 28, 2003. Revision received September 24, 2004. Accepted for publication September 28, 2004.
Journal of Dental Research, Vol. 83, No. 12,
930-935 (2004)
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for whisker composite with 74% fillers, higher than 1.13 ± 0.19 MPam
= 0.05). 



