Effect of aluminum oxide powder reinforcement on degree of conversion, monomer release and flexural strength of heat-cured acrylic resin

Objectives: Effect and correlation of aluminum oxide powder on degree of conversion, residual monomer and flexural properties of heat-cured acrylic resin specimens were studied. Materials and methods: Heat-cured acrylic resin and aluminum oxide powders were used. Specimens of specific dimensions from unreinforced and reinforced acrylic resins using stainless steel plates were prepared. Degree of conversion was determined using FTIR Spectrometer. Released monomer was measured using isocratic high-performance liquid chromatography. Flexural strength was tested using three point-bending test. Results: Aluminum oxide reinforcement showed increased degree of conversion than that of the unreinforced specimens. Released monomer from reinforced specimens was lower than that of unreinforced specimens. Deflection at fracture of reinforced specimens was lower than that of unreinforced specimens. Flexural strength was increased by addition of 2.5 % and 5% aluminum oxide. There was a positive correlation between degree of conversion and flexural strength. There was a negative correlation between degree of conversion and monomer release. Conclusions: Aluminum oxide powder increased degree of conversion and flexural strength but reduced monomer release and deflection at fracture. There was a positive correlation between degree of conversion and flexural strength. There was a negative correlation between degree of conversion and monomer release.


Introduction
Conventional heat-activated acrylic resin denture base materials are still the most commonly used denture base materials. Curing of the acrylic dough mix in the curing bath may affect the polymerization of the denture base resin material. The degree of conversion of the acrylic resin monomer is a measure of carbon-carbon double bonds (c=c) converted into carbon-carbon single bonds (c-c). As the temperature increases, the molecular mobility increases, leading to increased monomer polymerization. Polymerization of heat-cured acrylic resin by heat depends on time and temperature. Various amounts of unreacted methyl methacrylate monomer remain after curing of the denture bases [1].
The conversion of monomer to polymer may not be complete and a residual monomer is left in the polymeric material; this will affects the properties of the acrylic resin denture base materials [2]. Highperformance liquid chromatography coupled to an ultra-violet detector method was used to monitor the elution profile of methyl methacrylate monomer from poly (methyl methacrylate) resin produced by various polymerization modes. The un-polymerized methyl methacrylate monomer continued to leach out in the distilled water throughout the fiveweek period after curing [3]. methacrylate) resin. The leached amount into the artificial saliva from the resins was much higher, compared to that into water [4]. Residual monomer may diffuse from acrylic resin denture bases causing irritation or allergic reactions to the supporting tissues. Correct curing methods reduce residual monomer content in the denture bases. Correct curing cycles keep the residual monomer in the range of 1-3% that is well tolerated by vital tissues [5].
The acceptable curing method for acrylic polymerization is that capable to achieve the best properties of the acrylic resin denture bases, e.g. fracture toughness, static strength, flexural modulus and monomer release. It has been shown that high levels of residual monomer adversely affect acrylic resin properties like hardness & porosity [6]. One of the properties of acrylates is monomer release, which cause dimensional changes, thereby subjecting the material to internal stresses that may result in crack formation and fracture of the denture during service [7,8].
The acrylic resin denture base materials showed low strength, soft and fairly flexible, brittle on impact, and fairly resistant to fatigue. In evaluation of denture plastics, transverse strength measurements are used to a greater extent than either tensile or compressive strength, because this test more closely represents the type of loading in vivo.The geometry of denture bases is complex, so, the stresses can be concentrated in flaws on the surface of the denture base or in the frenum notches. The concentrated stresses lead to cracks in the denture base. The brittle nature of acrylic resin under its glass transition temperature (Tg) and its susceptibility to cyclic loading, fatigue fracture of dentures is a common clinical manifestation [5].
Conventional methods employed to reinforce a denture base polymers generally involve the use of metal wires or plates, fibers, metal powder or rubber toughening. To overcome the problem of denture fractures by improving the mechanical properties of the denture base polymer. The types of fibers that have been used to reinforce denture base polymers include aramid fibers,carbon/graphite fibers, ultra-high molecular weight polyethelene fibers and glass fibers [9].
This study was concerned with the reinforcing of the conventional heatcured acrylic resin powder with 2.5 % and 5% of aluminum oxide powder to test the reinforcing effects on degree of monomer conversion, monomer release, flexural strength and their correlations.

Testing the degree of monomer conversion
30 acrylic resin samples were prepared from the unreinforced, 2.5 % aluminum reinforced and 5% aluminum reinforced acrylic resin powder according to manufacturer's instructions and American Dental Association Specification # 12 [10]. The specimen ' s dimensions were, 50 mm length, 50 mm width and 1 mm thickness. Polyvinyl siloxane impressions were made using the putty form for the stainless steel plates. After setting of the impression, the impression molds were filled with melted baseplate wax and pressed using glass plate to obtain flat and smooth wax specimens. After hardening of the wax specimens, they were removed from the impressions and divided randomly into three groups, 10 samples each as follow: Group 1. Prepared from unmodified conventional heat-cured acrylic resin powder.
Group 2. Prepared from 2.5 % aluminum oxide powder modified heatcured acrylic resin. Group 3. Prepared from modified acrylic resin powder with 5 % aluminum oxide powder.
The wax samples were flasked in dental stone using the compression molding technique [11]. Washing was done for the wax specimens for 10 minutes in boiling water and sodium alginate separating medium was applied to cleaned stone molds. The acrylic resin powder / liquid ratio was mixed and then packed in the dough stage, packed in the denture flasks and pressed. The flasked specimens were immersed in water bath at room temperature in a thermostatically controlled unit. The temperature was raised slowly to 73 ± 1 o C for 90 minutes, and then elevated to the boiling point at 100 o C for 30 minutes. Bench cooling was done for the flasks before opening [5]. The cured acrylic resin plates were carefully removed from their molds and finished using a polishing machine with wet silicon carbide paper disk 600 grit size.
Each specimens was prepared for analysis with FTIR Spectrometer (FTIR-820 Ipc, Shimatzu) to determine the degree of monomer conversion. The aliphatic carbon-to-carbon double bonds (C=C) concentration of the uncured material was calculated at 1636 Cm -1 . A thin slice of the cured material was used to determine the concentration of the aliphatic C=C using the FTIR Spectrometer. The percent of monomer-topolymer is calculated in the cured specimens in relationship to the total C=C available in the uncured materials [1].
Resin cure was calculated by determining the proportion of weight percent methacrylate group (WPMG) available after curing (C) compared to the amount present in the uncured (U) solution using the following formula [1,12]: Where WPMGC is the weight percent methacrylate groups in cured resin and WPMGU is the weight percent methacrylate groups in uncured resin.

Testing of the released monomer
30 disc-shaped samples were prepared from the unreinforced and reinforced heat-cured acrylic resin powders, 10 samples each. The specimens dimensions is 50 mm in diameter and 3 mm thickness. All specimens were tested for monomer release according to the ISO 1567:2000. Each sample was stored in10 ml of deionized water in a sealed container in dark conditions at 37 o C for 7 days. The specimens were removed after storage period, and the amount of methyl methacrylate monomer was determined in the water after three extractions with 0.6 ml of n-hexane (Merck, Darmstadt, Germany). The final volume of extract was adjusted to 2.0 ml with n-hexane. The concentrations of released methyl methacrylate monomer was measured using isocratic highperformance liquid chromatography (HPLC; Waters, Milford, MA) with a reverse-phase column (LiChroCART 250-4 Cartridge, LiChrospher 100 RP-8 (μm) column, Merck. Acetonitrile (HPLC grade, Merck) with water (50:50) was the mobile phase; the flow rate was 1 ml/ min -1 , with detection at 254 nm. The peak area of methyl methacrylate monomer was calculated on the HPLC trace. Each specimens was measured three times. The amount of leached MMA was determined using a standard calibration curve with MMA concentrations of 1,5,10,100,500 & 1000 p.p.m. as controls [13,14].
Testing of the flexural strength 30 samples were prepared from the unreinforced and reinforced heatcured acrylic resin powders, 10 samples each. The transverse strength specimens dimensions were, 65 mm length, 10 mm width and 2.5 mm thickness. Specimens were stored in distilled water at room temperature for 24 hours. Flexural strength was tested using three point-bending test with a universal testing machine (Lloyd, type 500, England) with a cross head speed of 2 mm/min until fracture. The load was applied at the center of the specimen. The machine is computerized to calculate the flexural strength from the applied load and the deflection at fracture from the introduced data to the testing machine.

Statistical analysis:
The tabulated data were exposed to one way ANOVA test to detect the significant difference among the tested materials. The test with ANOVA significance was exposed to LSD test to detect the significant difference between groups at p ≤ 0.05.

Results
Means and standard deviations of percent monomer conversion of unreinforced and aluminum oxide reinforced heat-cured acrylic resins are presented in Table 1. One-way ANOVA test showed no significant difference among the tested groups (P ≥ 0.05). Aluminum oxide reinforced groups showed insignificant increased degree of monomer conversion than that of the unreinforced group. Means and standard deviations of monomer released (ppm) of unreinforced and aluminum oxide reinforced heat-cured acrylic resins are presented in Table 2. One-way ANOVA test showed significant difference among the tested groups (P ≤ 0.05). The statistical analysis of the results indicated that there were significant differences between the unreinforced and aluminum oxide reinforced groups. 5% aluminum reinforced group showed significantly lower monomer release than that of the unreinforced and 2.5 % aluminum oxide reinforced group. Also, 2.5 % aluminum reinforcement significantly reduced the released monomer when compared to the unreinforced heat-cured acrylic resin. Means and standard deviations of specimen ' s deflection (mm) at fracture of unreinforced and aluminum oxide reinforced heat-cured acrylic resins are presented in Table 3. One-way ANOVA test showed significant difference among the tested groups (P ≤ 0.05). The statistical analysis of the results indicated that there were significant differences between the unreinforced and aluminum oxide reinforced groups. 2.5 % and 5% aluminum reinforcement were significantly reduced the deflection at fracture of the heat-cured acrylic resin.  Table 3. Means and standard deviations of specimen's deflection at fracture of unreinforced and aluminum reinforced heat-cured acrylic resins (mm).
Means and standard deviations of flexural strength (Mpa) of unreinforced and aluminum oxide reinforced heat-cured acrylic resins are presented in Table 4. One-way ANOVA test showed significant difference among the tested groups (P ≤ 0.05). The statistical analysis of the results indicated that 2.5 % and 5% by weight of aluminum oxide powder reinforcement were significantly increased the flexural strength of the heat-cured acrylic resin (P ≤ 0.05). There was high positive correlation between the degree of conversion and flexural strength. There was negative correlation between degree of conversion and monomer release   Table 5. Correlations between the degree of conversion, monomer release, deflection at fracture and flexural strength of heat-cured specimens.

Discussion
Conventional heat-cured acrylic resins are still the predominant denture base materials in use. In the mouth, properties and functional efficiency of applied acrylic resins depend on internal factors related to the methods and conditions of polymerization and on external factors that are related to the environment in which the material is placed [15]. Efforts must be made to improve the handling properties, transverse deflection, and water sorption of radiopaque denture base materials. These materials has low strength, soft and fairly flexible, brittle on impact, and fairly resistant to fatigue failure [16].
Heat-cured acrylic resin composed mainly from Methyl methacrylate monomer that polymerized by activation of the monomer by heat to form poly Methyl methacrylate polymer [16]. Polymerization is followed by conversion of methyl methacrylate (MMA) to PMMA. During polymerization reaction of acrylic resins, not all the monomers are converted into polymers, and therefore some unreacted monomers called residual monomers are left [15].
The residual monomer content of a properly processed denture is less than 1%. Irritation is slightly more common and is related to residual monomer. Irritation reactions are relatively rare and the reactions to the residual monomer should occur shortly after prosthesis delivery. As previously noted, the amount of residual monomer in processed polymethyl methacrylate is extremely low [17].
In the evaluation of denture plastics, flexural strength measurements are used to a greater extent than either tensile or compressive strength, because this test more closely represents the type of loading in vivo. Flexural strength is determined by applying an increasing load until fracture at the center of a test specimen. Flexural strength is therefore a combination of tensile and compressive strength and includes some of the elements of proportional limit and elastic modulus. A transverse deflection test has been used to evaluate denture base resins [16].
The results of the present research paper showed slight increase of degree of conversion of aluminum oxide reinforced heat-cured acrylic resins. This may be due to the aluminum powder is a good conductor material that help rising of temperature within the acrylic dough during polymerization. Polymerization of PMMA by heat may be affected by a variety of time and temperature parameters. The conversion of monomers to polymers is not complete, and some unreacted monomers, namely residual monomers, are left in the PMMA. Residual monomer is a wellknown plasticizer and affects the physical and mechanical properties of acrylic resins. Also, residual monomer diffused from acrylic resin has been implicated as a primary irritant and a sensitizer that can cause an allergic eczematous reaction on both the skin and the oral mucosa [18].
The released monomer of aluminum oxide reinforced heat-cured acrylic resins was less than that of the conventional unreinforced group. This may be due to increasing the degree of monomer conversion in the present study. Polymerization time and temperature affect the residual monomer content, which is usually higher in autopolymerizing than in heat-polymerizing acrylic resins [19]. It has been stated that there is an inverse relationship between the degree of conversion and the residual monomer content, thus the higher the former the lower the latter [20].