Stainless Steel Mold Research Articles

Performance analysis of cyanoacrylate bonded optical fiber 2 × 2 acoustic couplers for sensing applications

In this paper the behavior of a cyanoacrylate (CA) bonded optical fiber acoustic signal coupler will be studied in detail. A stainless-steel mold was used to create a 2×2 CA coupler that transfers guided waves between two optical fibers. Four FBGs placed at each port were used to assess the repeatability, signal behavior, and performance of the coupler produced. Signal propagation through the network was mapped to determine how the initial acoustic signal traveled and subdivided through the fiber network. To examine the repeatability of the signal coupler interaction, the experiments were performed multiple times. Finally, the acoustic energy transferred through the coupler’s paths was calculated to assess the performance of the 2×2 coupler. The coupler successfully and repeatably transferred an acoustic signal from one optical fiber to another; however, the performance associated with the current coupler design was limited by relatively large excess and return losses. Improvements to the CA coupler design are then proposed from the results.

Performance of Geopolymer Insulation Bricks Synthesized from Industrial Waste

In the current work, aluminum dross from the aluminum industry and fired-clay brick waste (Homra) were combined with alkaline activators (Na2SiO3/NaOH) with varying molarities of NaOH to create insulating geopolymer bricks. An alkaline activator with an (S/L) ratio of 3/1 was combined with Homra to replace it partly. The mixture was then molded into 50 × 50 × 50 mm3 stainless steel molds. Water absorption, compressive strength, bulk density, and apparent porosity of the produced geopolymer were measured at various curing durations and NaOH molarities. The findings showed that adding more aluminum dross waste replacement leads to a decrease in bulk density and compressive strength and an increase in the creation of pores that improve the produced bricks’ ability to insulate against heat. Using 8 M of NaOH after 28 days, the findings revealed that 3% aluminum dross waste replacement has a compressive strength of about 8.6 MPa, water absorption of 14.6%, bulk density of 1.307 g/cm3, and thermal conductivity of 0.32 W/m·K. The Egyptian standard, ASTM C62, satisfies these outcomes. Using DesignBuilder energy simulation software version 6.1.06, the constructed insulating brick under ideal circumstances was utilized to calculate its contribution performance in energy consumption. The annual energy consumption was reduced by about 21% compared to traditional hollow cement bricks.

Comparison of Various Surface Treatment Procedures on the Roughness and Susceptibility to Staining of Provisional Prosthodontic Materials.

Esthetically pleasing temporary prostheses are often necessary for extended periods in a variety of clinical scenarios. Adjustments to the occlusion or margins are commonly needed before cementing the temporary prosthesis. Therefore, it is clinically necessary to repolish the rough surface to avoid biological and esthetic issues associated with rough surfaces. The purpose of this in vitro study was to assess and compare the impact of various polishing protocols on the surface roughness and color stability of three resin materials used for provisional crowns. A total of 150 specimens were fabricated from auto-polymerizing polymethyl methacrylate, bis-acryl composite, and Methyl methacrylate-LC resin using a stainless steel mold. Each material group was divided into five groups (n = 10) based on the applied surface treatment: positive control group (G1): no roughening or surface treatment, Negative control group (G2): acrylic bur-roughened surface without any polishing, the different surface treatment groups of silicon carbide and aluminum oxide stone polishing (G3), diamond-coated rubber twist (G4), and Surface Glaze (G5). An optical profilometer was used to assess the surface roughness of all samples. After undergoing 6000 cycles of thermocycling followed by immersion in a coffee solution for 15 days at 37 °C, color parameters were measured using a spectrophotometer both before and after a storage period to evaluate color differences. A two-way ANOVA test with α = 0.05 significance level was carried out to determine the impacts of both the materials utilized and the polishing protocol. Among the three types of resin examined, the bisacryl group exhibited superior surface quality in positive control groups, while PMMA resin demonstrated higher polishability. The diamond-coated rubber twits resulted in lower Ra values of 0.36 (0.01) µm, 0.52 (0.11) µm, and 0.28 (0.05) µm for PMMA, BAMA, and MMLC resins, respectively. The application of photo-polymerized surface glaze led to a plaque accumulation threshold of 0.2 µm across all resin groups. The greatest mean color change occurred in the negative control group, indicating a propensity for more staining on rougher surfaces. The Bisacryl resin exhibited higher ΔE values, whereas PMMA showed better color stability. The lowest ΔE values were found when the surface glaze was applied to all of the provisional crown resins. Untreated Bisacryl resin exhibited the lowest Ra values, while PMMA resins demonstrated superior surface morphology after polishing. PMMA provisional crown resins showed increased resistance to staining. The use of surface glaze enhanced both smoothness and color stability on the surfaces.

Thermal properties and microstructure of Al–Sn alloys

The Al–Sn alloys feature excellent wear and corrosion resistance, along with good mechanical properties. They are mostly used as bearing materials. However, the application of these alloys as phase change materials (PCMs) for thermal energy storage (TES) has recently been suggested. To assess the adequacy of these alloys in a given area, a detailed evaluation of their thermal properties is required. In the present study, Al–Sn alloys with 11.7, 22.4, 32.8, 41.1, and 53.4 at.% Sn were produced by melting of pure metals. The melt was continuously stirred to avoid segregation, after which casting was carried out in a stainless steel mold. The obtained ingots had a homogeneous microstructure without the appearance of cracks and pores. The thermal diffusivities of the solid Al–Sn alloys in the temperature interval 25–150 °C were measured using the light flash method. The densities at room temperature were measured by the Archimedes method, and the specific heat capacities at different temperatures were calculated using the calculation of phase diagrams (CALPHAD) method. Then the thermal conductivities for studied Al–Sn alloys were obtained by the specific conversion equation. The phase transition temperatures and related heat effects were studied using differential scanning calorimetry (DSC). Variations of thermal conductivity with composition and temperature were determined as well as variation of latent heat of fusion with alloy composition. Moreover, the microstructures and phase compositions of the alloys were examined using scanning electron microscopy (SEM) combined with energy dispersive spectrometry (EDS). The present research results provide important information on the thermal properties and microstructure of the Al–Sn alloys for designing new PCM for thermal energy storage.

Imparting semi-permanent demoldability to stainless steel mold using surface-initiated solution polymerization of stearyl methacrylate

The growing market demand for compact and precisely-designed polymeric products has raised challenges during the demolding stage of manufacturing. An increased contact area between the product and the mold increases adhesion, which reduces dimensional stability and aesthetics. Conventional solutions like surface roughness improvement or release agent coatings suffer from reduced productivity and impurity-related issues affecting mechanical properties. To address these challenges, we imparted the semi-permanent demoldability to a stainless steel (SUS) mold by polymerizing stearyl methacrylate monomer on its surface using a surface-initiated solution polymerization technique. The polymerization state was confirmed through Fourier transform infrared spectroscopy and field emission scanning electron microscopy. The demoldablity was investigated using the appropriately-designed lap shear tests to simulate the demolding stage of epoxy resin-filled SUS mold to ensure sufficient performance compared with the neat and commercial release agent (RA) treated molds, and durability of the demoldability was confirmed via repetitive single-lap shear tests simulating the molding and demolding processes. The surfaced polymerized mold exhibited excellent demoldability with 96.5 % improvement over the neat one, and showed excellent durability over 5 repeated molding cycles, while the commercial RA showed significant degradation of demoldability. Furthermore, the mechanism of demoldability enhancement using the proposed surface polymerization was investigated by characterization of the surface dewetting pattern and contact angle measurements of the epoxy resin on the modified mold surface.

Assessing one-shade composite resin color stability in response to everyday drinks

ObjectiveThe aim of our study was to measure the color changes in one-shade composite resins when exposed to common drinks, such as tea, cola and coffee.Materials/MethodsIn our study, Omnichroma, Vitrra APS Unique, GC A’chord and Charisma Diamond One composite resins were used. Composite resins were placed in stainless steel molds with depths of 2 mm and diameters of 5 mm. Ten specimens were immersed in tea, 10 specimens were immersed in coffee, 10 specimens were immersed in cola and 10 specimens were immersed in distilled water in an incubator at 37 °C for 14 days. Color measurements were performed at the beginning of the study and after 24 h and 14 days. Color values ​​were measured using a CIE L*a*b* system with a spectrophotometer device. Color and translucency changes were calculated and data analyzed using one-way ANOVA, two-way ANOVA, and post-hoc Tukey test (p < 0.05).ResultsThe greatest color changes occurred in the tea and coffee groups; the smallest color change occurred in the control group. After 14 days, the greatest color change was observed in the Charisma + Coffee group; the smallest color change was observed in the Omnichroma + Water group. The transparency and contrast ratios changed in all groups, and the smallest change occurred in the Omnichroma control group.ConclusionSignificant differences were found in the composite color changes after immersion in beverages. The color variations significantly differed depending on the beverage in which the specimens were immersed. The initial contrast ratio was markedly different from the examined materials.Clinical significanceThe study emphasizes the significance of common beverages on the color stability of one-shade composite resins, underlining the need of appropriate material selection for long-term aesthetic effects in one-shade composite resin restorations.

Effect of Instrument Lubricant on Mechanical Properties of Restorative Composite.

Using a wetting resin or adhesive system as an instrument lubricant when placing composite layers is commonly practiced to improve handling. This study investigated whether instrument lubricants affected strength, stiffness, or hardness. Composite beams (TPH Spectra) were fabricated using a stainless steel mold (25×2.5×2 mm) in two steps, where the second half (12.5 mm) was added and cured against a cured first half (n=15). The composite surface at the open end of the first half was smoothed using an instrument lubricated with wetting resin (Ultradent) or universal adhesive (ScotchBond Universal), enough to prevent sticking, or without lubrication. An additional beam of each group was characterized using scanning electron microscopy. Monolithic specimens were also fabricated. After 24 hour storage (37°C, 100% humidity), the beams' flexural strength and stiffness were determined by four-point bending. Vickers surface hardness was measured on 24-hour composite samples in 2 mm deep acrylic cavities, cured after the surface was smoothed with the two instrument lubricants or no lubricant (n=10). Hardness was remeasured after finishing with a series of contouring and polishing discs. Data were statistically analyzed using ANOVA followed by Student-Newman-Keuls post hoc test at 0.05 significance level. There were significant differences (p<0.001) in flexural strength and stiffness among groups. While strength and stiffness were not affected by using a wetting resin as instrument lubricant, use of a universal adhesive increased strength and stiffness significantly, achieving monolithic values. Scanning electron micrographs showed less porosities at the interface when using instrument lubricants. Surface hardness was significantly reduced in groups in which instrument lubricants were used, but finishing/polishing restored original hardness (p<0.001). Lubricating an instrument with a wetting agent did not adversely affect physical or surface properties, provided the surface was finished and polished. If a universal adhesive was used as lubricant, the strength and stiffness of a layered composite could be increased, reaching monolithic values.

Evaluation of the pH and Antibacterial Efficacy of Mineral Trioxide Aggregate With and Without the Incorporation of Titanium Tetrafluoride.

Introduction Microorganisms play an important role in causing inflammation in the pulp and periapical regions. Even after undergoing chemo-mechanical procedures during root canal treatment, bacteria may persist within dentinal tubules, posing a risk of disease recurrence. Mineral trioxide aggregate (MTA), introduced as a dental material, has been investigated as a potential antibacterial agent since its early use. Calcium and phosphorus are the primary ions in MTA, and their antibacterial characteristics are attributed to the release of calcium hydroxide through surface hydrolysis of calcium silicate components. Previous studies have shown that MTA has limited antimicrobial properties. Several alterations have been made to enhance the biological properties of MTA, such as incorporating nanoparticles made from silver, zinc, gold, and titanium. Therefore, in this study, titanium tetrafluoride (TiF4) was added to MTA in an effort to enhance its antimicrobial properties. Aim To compare and evaluate the antibacterial efficacy of MTA after the incorporation of TiF4. Materials and methods A total of 56 samples were made by mixing MTA with different weight proportions of TiF4 (1 wt%, 2 wt%, and 3 wt%). Out of these, 28 samples were taken to test each of the following properties: antibacterial efficacy and pH. The specimens were prepared using stainless steel molds of recommended dimensions for testing the pH. The pH was evaluated using a pH meter, and the antibacterial efficacy was assessed using the direct contact test. Data regarding the antibacterial efficacy and pH of MTA with various proportions of TiF4 were investigated for normality using the Kolmogorov-Smirnov test and assessed for normal distribution. The antibacterial properties among the four groups were analyzed using one-way analysis of variance (ANOVA), followed by pairwise multiple comparisons using Tukey's Honest Significant Difference test. The level of statistical significance was determined at p ≤ 0.05. MTA, when incorporated with TiF4, showed enhanced antibacterial properties. Results On day 1, the group treated with MTA containing 3% TiF4 demonstrated the strongest antibacterial effectiveness, with a mean of 4.67 ± 0.04 colony-forming units (CFU)/mL × 10^8. However, the group treated with plain MTA had the lowest mean values, at 5.67 ± 0.25 CFU/mL × 10^8. On day 1, the MTA group with 3% TiF4 also had the highest mean pH values (11.90 ± 0.05), while the plain MTA group had the lowest mean pH values (11.64 ± 0.78). On day 7, the MTA group with 3% TiF4 had the highest pH value (12.85 ± 0.08), whereas the plain MTA group had the lowest pH value (11.92 ± 0.09). Conclusion The inclusion of TiF4 resulted in an augmentation of the antibacterial efficacy of MTA against Enterococcus faecalis (E. faecalis). Hence, the integration of TiF4 into MTA can be considered a promising development against E. faecalis during endodontic procedures.

Optimization of Multiphase Flow and Initial Solidification Behaviors in a Stainless Steel Mold by SEN Design

Optimization of Multiphase Flow and Initial Solidification Behaviors in a Stainless Steel Mold by SEN Design

Evaluation of the Impact of Irradiance Lamps and Storage Media on Elution of TEGDMA from Dental Composites.

The aim of this study was to evaluate and compare the effect of irradiance light and storage media on the elution of triethylene glycol dimethacrylate (TEGDMA) from conventional Filtek Z350XT 3M ESPE and two bulk-fill composites Shofu Beautifil-Bulk and Filtek Bulk fill flowable 3M ESPE using high-performance liquid chromatography (HPLC). Shofu Beautifil-Bulk, Filtek Bulk fill flowable 3M ESPE, and Filtek Z350XT 3M ESPE were the three types of composites used in this study. Disk shaped samples of 4-mm thickness and 10-mm diameter were fabricated using a stainless steel mold and were polymerized using light emitting diode (LED) and quartz tungsten halogen (QTH) lamps. After polymerization, the samples were immersed in ethanol, artificial saliva with betel quid extract, and distilled water for 1, 7, and 30 days, respectively. The elution of monomer TEGDMA was evaluated using HPLC. To evaluate the mean concentration difference, mixed way analysis of variance (ANOVA) was applied. Between different light, materials, and within the time duration, Tukey's post hoc test was used. A p value of 0.05 was considered significant. During the first day of storage, a significant amount of monomer TEGDMA elution was seen in all the materials. The highest values observed to be in the disks cured with QTH lamp. However, the highest elution was seen when the disks were immersed in ethanol/water solution. While the most stable medium was distilled water, artificial saliva with betel nut extract also had a significant effect on the elution of TEGDMA. The highest value obtained was of Filtek Bulk fill flowable 3M ESPE after 30 days of immersion in both LED and QTH cured disks. Filtek Bulk fill flowable 3M ESPE shows better properties in relation to the release of monomer TEGDMA as it releases less amount of monomer in the storage media. The release of monomer was highest in ethanol as compared to artificial saliva and distilled water with the passage of time.

Evaluation of Flexural Strength and Microhardness of Different Type Glass Ionomer Cements

Abstract Purpose: The aim of this study is to evaluate and compare flexural strength and microhardness of different types of glass ionomer cements (Fuji IX GP® Fast, Riva LC HV, EQUIA Forte Fil). Materials and Methods: A total of 30 samples (n = 10) were prepared for microhardness test, and an additional total of 30 samples (n = 10) were prepared for the flexural strength test. Customized stainless steel molds (25×2×2 mm³) were produced for the flexural strength test, and 10 mm and 2 mm plexiglass molds were produced for the microhardness test. The prepared samples were stored in distilled water in a dark bottle at 37 °C (±1 °C) for 24 hours. A three-point bending test was performed using a universal testing device, and the maximum force values required to fracture the samples were determined in Newton by the device after the fracture. For the Vickers microhardness test measurements were made from different areas of the upper surfaces of each sample and the average of five measurements was calculated in MPa. Results: When comparing the flexural strength values, EQUIA Forte Fil group observed the highest flexural strength value, while Riva LC HV group had lowest flexural strength value. When comparing the microhardness values, EQUIA Forte Fil group showed the highest microhardness value, whereas Riva LC HV group observed the lowest microhardness value. Conclusion: The use of EQUIA Forte Fil, which has the highest microhardness and flexural strength values, and similarly strengthened glass ionomer cements may enhance clinical success. Key Words: glass ionomer cements; microhardness; flexural strength

Mineralogy and geotechnical properties of alkaline-activated kaolin with zeolitic tuff and cement kiln dust as landfill liners

Mixtures of variable proportions of kaolin, quartz sand, zeolitic tuff, and cement kiln dust were blended while adding an 8 M sodium hydroxide (NaOH) solution to allow alkali-activation of kaolin and achieve the optimum strength. This study investigated the mineralogy, microstructure, and geotechnical properties of the prepared mixtures. The aim was to produce a sustainable, environmentally friendly landfill liner. The samples were compacted in stainless steel molds to a maximum dry density and optimum moisture content, extruded from the molds, and left to cure in an oven at varying temperatures from 40°C to 80°C for 24 h. The investigations included XRD, SEM, unconfined compressive strength, and hydraulic conductivity tests. Test results showed the development of a hydroxysodalite binder due to the alkali reaction of kaolin, which caused an increase in strength ranging from 20 to 25 MPa depending on the curing temperature. Alkaline activation was effective even at temperatures as low as 40°C. A mixture of 100 units of kaolin, 45 units of sand, 45 units of zeolitic tuff, and 10% by weight cement kiln dust (CKD) with an 8 M sodium hydroxide activator was found to best achieve the required strength and hydraulic conductivity of 10−9 m/s for the landfill liner. The zeolitic tuff with high cation exchange capacity, available in the mixture, absorbs contaminants in the leachate and prevents pollution of the groundwater. The use of cement kiln dust contributes to enhancing strength and solving an acute environmental problem.

Microscopic Comparison of the effect of Three Polishing Systems on a Nanofiller Composite Resin

In restorative dentistry, selection of materials is decisive to obtain optimal aesthetic results, in the case of dental resins, the size characteristics and particle distribution of the different polishing systems, constitute a factor considerably influences the results. Objective: The purpose of the present research work was to compare three systems employed to polishing composite resin, documenting the results at the microscopic level, to identifying which of them showed better results concerning the roughness. Material and methods: Three polishing systems were evaluated: Soflex from 3M®, Optra Pol and Astrobrush from Ivoclar® Vivadent and Jiffy Hishine from Ultradent, employing the LSM 700 Confocal Microscopy System, also roughness was observed and registered on the surface of a nanofiller resin Tetric Evoceram Ivoclar® Vivadent inserted in stainless steel molds. Results: The roughness mean observed were as follows: 13.95μm for Soflex of 3M®, 13.45μm for Optra Pol of Ivoclar® and 8.05μm for Jiffy Hishine Ultradent. All data recorded in Microsoft Excel 2010 IBM STATISTICS, determinated statistical differences between the groups of Ultradent®. Conclusion: The lowest roughness corresponded to Ultradent with values of 8.01μm.

Surface Degradation of Ion-releasing Restorative Materials With Cariogenic Challenge.

This study examined the influence of cariogenic environments on the surface roughness of ion-releasing restorative materials (IRMs). Custom-made stainless steel molds with holes of 5 mm × 2mm were used to fabricate 60 disc-shaped specimens of each of the following materials: Activa Bioactive (AV), Beautifil Bulk Restorative (BB), Cention N (Bulk-fill) (CN), and Filtek Z350XT (FZ) (Control). Baseline surface roughness (Ra) measurements were obtained using an optical 3D measurement machine (Alicona Imaging GmbH, Graz, Austria). The specimens were then randomly divided into five subgroups (n=12) and exposed to 10 ml of the following mediums at 37°C: distilled water (DW), demineralization solution (DM), remineralization solution (RM), pH cycling (PC) and air (AR) (control). Ra measurements were again recorded after one week and one month, followed by statistical evaluations with two-way analysis of variance (ANOVA) to determine interactions between materials and mediums. One-way ANOVA and post hoc Games Howell tests were performed for intergroup comparisons at a significance level of 0.05. Mean Ra values ranged from 0.085 ± 0.004 (µm) to 0.198 ± 0.001 µm for the various material-medium combinations. All IRMs showed significant differences in Ra values after exposure to the aqueous mediums. The smoothest surfaces were observed in the AR for all materials. When comparing materials, AV presented the roughest surfaces for all mediums. All IRM materials showed increased surface roughness over time in all cariogenic environments but were below the threshold value for bacterial adhesion, except for AV 1-month post immersion with pH cycling. Therefore, besides AV, the surface roughness of IRMs did not deteriorate to an extent that it is clinically relevant.

Effect of Different Disinfecting Agents on Surface Roughness and Color Stability of Heat-cure Acrylic Denture Material: An In Vitro Study.

The current study aimed to determine the impact of three different disinfectants on the surface roughness and color stability of heat-cure acrylic denture material. Using a stainless-steel mold, disc-shaped wax patterns with dimensions of 10 mm in diameter and 2 mm thick (in accordance with ADA Specification No. 12) were created and prepared for a total of 75 acrylic samples. Dimensions of all 75 acrylic samples were checked with a digital Vernier caliper. About 25 samples of denture base material were immersed in three different chemical disinfectants: Group I: immersed in chlorhexidine gluconate solution, group II: immersed in sodium hypochlorite solution, and group III: immersed in glutaraldehyde solution. All samples were scrubbed daily for 1 minute with the appropriate disinfectant and submerged for 10 minutes in the same disinfectant. Between disinfection cycles, samples were kept in distilled water at 37°C. Color stability was measured using a reflection spectrophotometer. Surface roughness values were measured by a profilometer at baseline following 15 days and 30 days. After 15 days, the color stability was better in chlorhexidine gluconate solution group (4.88 ± 0.24) than sodium hypochlorite solution (4.74 ± 0.18) and glutaraldehyde solution group (4.46 ± 0.16). The mean surface roughness was less in glutaraldehyde solution group (2.10 ± 0.19), followed by chlorhexidine gluconate solution group (2.48 ± 0.09) and sodium hypochlorite solution group (2.64 ± 0.03). After 30 days, the color stability was significantly better in chlorhexidine gluconate solution group (4.40 ± 0.02), followed by sodium hypochlorite solution (4.06 ± 0.16) and glutaraldehyde solution group (3.87 ± 0.17). The mean surface roughness was significantly lesser in glutaraldehyde solution group (2.41 ± 0.14), followed by chlorhexidine gluconate solution group (2.94 ± 0.08) and sodium hypochlorite solution group (3.02 ± 0.13). In conclusion, the color stability was significantly better in chlorhexidine gluconate solution group than sodium hypochlorite solution and glutaraldehyde solution group. But the surface roughness was significantly lesser in the glutaraldehyde solution group, followed by the chlorhexidine gluconate and sodium hypochlorite solution group. The maintenance of the prosthesis requires the use of a denture disinfectant; therefore, it is crucial to select one that is effective but would not have a negative impact on the denture base resin's inherent characteristics over time. How to cite this article: Kannaiyan K, Rakshit P, Bhat MPS, et al. Effect of Different Disinfecting Agents on Surface Roughness and Color Stability of Heat-cure Acrylic Denture Material: An In Vitro Study. J Contemp Dent Pract 2023;24(11):891-894.

Experimental Investigations on Cylindrical GFRP Composite Pipes under Compression Loading

In a wide variety of aerospace applications have the mechanical properties of a thin cylindrical shell are important. Thin cylindrical shell structures are used to store a small and large quantity of fluids and solids. Glass Fabric reinforced epoxy composite is used to prepare the thin cylindrical pipes with different diameters and varying thickness of the composite pipes. The additives as glass flakes are added with 5%, 10% and 15% of the resin content in the matrix. The rolled composites specimens are prepared with the stainless steel (SS) mould. Experiments are test on Universal Testing Machine under lateral compression test to study the breaking load and compressive strength of the specimens. The failure modes are also observed.

The Depth of Cure, Sorption and Solubility of Dual-Cured Bulk-Fill Restorative Materials.

This study aimed to examine depth of cure (DoC), mass change, water sorption and solubility of dual-cured bulk-fill restorative materials (Surfil One and Activa) in comparison with a light-cured bulk-fill composite (Filtek One Bulk-Fill) and a resin-modified glass ionomer (Fuji II LC). Twenty specimens were prepared of each material using stainless steel molds designed with a slot (8 × 4 × 2 mm) and irradiated for either 20 or 40 s. The Vickers hardness (VHN) was measured at every 0.5 mm to assess the DoC after 24 h of storage at 37 °C. The depth of cure was reported as the depth corresponding to 80% of the maximum Vickers hardness. Disc-shaped specimens were prepared of each material (n = 5) to investigate mass change, sorption and solubility after 4 months of water storage. The data were analyzed using a two-way and one-way analysis of variance (ANOVA) followed by the Tukey post hoc test (p ≤ 0.05). Fuji II LC had the greatest DoC while Activa had the lowest. The two different irradiation times did not demonstrate a significant difference in DoC for all dual-cured materials (p > 0.05). Fuji II LC had the highest sorption while Filtek One showed the lowest. Surefil One and Fuji II LC had a negative solubility. This study concluded that dual-cured materials showed different depth of cure values despite having the same setting reaction. Both materials exhibited a high water sorption, which might jeopardize their dimensional stability and effect their clinical performance.

Effect of Aging on Hardness of Glass Ionomer, Resin-Modified Glass Ionomer, Giomer and Compomer Dental Restorative Materials

Objective: To assess deionized water's aging effect on the hardness of four direct tooth colored dental filling materials i.e., Glass Ionomer Cement, Resin Modified Glass Ionomer, Giomer and Compomer.Study Design: An in vitro experimental study performed in triplicates.Place and Duration of Study: The study was carried out at PG Laboratory, Department of Science of Dental Materials, Army Medical College, Rawalpindi, Pakistan from February 2023 to August 2023.Methods: Three disc-shaped samples (n=3) of 10 mm diameter and 1 mm thickness of each restorative material were prepared using stainless steel molds per manufacturer's instructions. These disc-shaped samples were then suspended in a 15 mL conical centrifuge tube containing 10 mL deionized water, followed by incubation in a Forced Convection Laboratory Oven at 37 C where these were allowed to age over a period of 1-2 years. Vickers Hardness of each sample was then checked at two-time intervals, i.e., after 24 h setting and after 2.5 years of ageing through the Micro Vickers Hardness Tester calibrated at 1Kgf (9.80 N) with dwell time of 10 seconds and light intensity 10. Results: After one day (24 h) aging in deionized water, maximum mean Vickers hardness number (VHN) was exhibited by Compomer (539.83±58.08 VHN) and least by GIC (175.75±24.47 VHN). After aging the sample for 912 days, maximum mean VHN was observed for GIC (420.67±99.66 VHN) and least by Compomer (354.33±9.22 VHN). Conclusion: RMGIC sustains its hardness on aging, hardness of GIC increases while that of Giomer and Compomer decreases upon aging.&#x0D; How to cite this: Gul H, Nayyer M, Junaid Y, Pasha M, Ejaz T, Liaqat U, Hassan SH. Effect of Aging on Hardness of Glass Ionomer, ResinModified Glass Ionomer, Giomer and Compomer Dental Restorative Materials. Life and Science. 2023; 4(4): 438-444. doi: http://doi.org/10.37185/LnS.1.1.437

Influence of Three Different Denture Cleansers on Surface Roughness and Strength of Heat-polymerizing Resin: An In Vitro Study.

The purpose of the current study was to evaluate the impact of three different denture cleansers on the strength and surface roughness of heat-polymerizing resin. A total of 120 resin discs (10 mm in diameter and 2 mm thick) were created using a stainless steel mold for surface roughness testing and flexural strength testing (in accordance with the American Dental Association (ADA) Specification No.12). Samples were divided into one of three groups (40 samples in each group): group I: Clanden, group II: Clinsodent, group III: Fittydent. Samples were immersed in denture-cleansing solutions for 30 minutes every day, and this process was repeated over a period of 15 days. Samples were stored in distilled water at room temperature in between the immersions. A surface analyzer was utilized to compare the surface roughness of each sample before and after immersion treatments. For recording flexural strength, each sample was subjected to three-point bending test by mounting samples on Universal testing machine. Comparing mean values between groups using one-way ANOVA and the Tukeys honest significant difference (HSD) post hoc test. A significance level of 0.05 was used for all statistical calculations Results: After 15 days, the maximum change of mean surface roughness of heat-polymerizing resin was found in Clanden denture cleanser group (2.64 ± 0.12) followed by Clinsodent group (2.26 ± 0.09) and Fittydent group (1.92 ± 0.06). After 15 days, the maximum change of mean flexural strength changes of heat-polymerizing resin was found in Clanden denture cleanser group (94.78 ± 0.14), followed by Fittydent group (98.64 ± 0.03) and Clinsodent group (99.26 ± 0.21). Within the limitation, the current study concluded that changes were observed in surface roughness and flexural strength of all heat-polymerizing resin samples after immersion in all three denture cleansers; but least surface roughness and flexural strength changes were observed with the Fittydent cleanser group and Clinsodent group, respectively. Cleaning dentures is crucial for maintaining both the prosthesis and oral health; therefore, it is necessary to select a cleanser that is effective without negatively affecting the base resin's qualities over time.

Effect of Gingival Hemostatic Agents on the Surface Detail Reproduction and Dimension Stability of Three Elastomeric Impression Materials.

This study aimed to evaluate the effects of aluminum chloride based hemostatic agents on the surface detail reproduction and dimension stability. Three impression materials were investigated after contaminated with three commercial astringents with different concentration of aluminum chloride. The specimens from three impression materials were fabricated with a stainless-steel mold that followed the American Dental Association specification no.19. The mold was preliminarily contaminated with three hemostatic agents racestyptine, Dryz, and Expasyl™-and 80 specimens from each impression material-polyvinylsiloxane (PVS), polyether, and polyvinylsiloxane ether (PVSE), were fabricated and subjected to each astringent. The surface detail reproduction was examined using a stereomicroscope at 4x magnification, and the dimensional stability was analyzed at 24 hr with a measuring microscope. The surface detail data were statistically analyzed with Fisher's test at a significance level of 0.05. The dimensional stability data were analyzed using two-way ANOVA and Tukey's test at a significance level of 0.05. Aluminum chloride hemostatic agents can affect the surface detail reproduction of impression materials differently (p < 0.05). Thus, the first null hypothesis was rejected. PVS showed the highest percentage of satisfactory surface detail regardless of the hemostatic agent used in this study. PVSE showed a reduced percentage of satisfactory surface detail when the concentration of aluminum chloride was high. The three hemostatic agents affected the dimensional stability of each material differently (p < 0.05). Therefore, the second null hypothesis was also rejected.