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Lead (Pb) halide perovskite nanocrystals, with the general formula APbX3 , where A=CH3 NH3+ , CH(NH2 )2+ , or Cs+ and X=Cl- , Br- , or I- , have emerged as a class of materials with promising properties due to their remarkable optical properties and solar cell performance. However, important issues still need to be addressed to enable practical applications of these materials, such as instability, mass production, and Pb toxicity. Recent studies have carried out the replacement of Pb by various less-toxic cations as Sn, Ge, Sb, and Bi. This variety of chemical compositions provide Pb-free perovskite and metal halide nanostructures with a wide spectral range, in addition to being considered less toxic, therefore having greater practical applicability. Highlighting the necessity to address and solve the toxicity problems related to Pb-containing perovskite, this review considers the prospects of the Pb-free perovskite, involving synthesis methods, and properties of them, including advantages, disadvantages, and applications.
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Quantum dots (QDs) have attracted much attention and exhibit many attractive properties, including high absorption coefficient, adjustable bandgap, high brightness, long-term stability, and size-dependent emission. It is known that to obtain high-quality luminescent properties (i.e. emission color, color purity, quantum yield, and stability), the synthesis parameters must be precisely controlled. In this work, we have constructed a database with CdTe aqueous synthesis parameters and spectroscopic results and applied machine learning algorithms to better understand the influence of the main synthesis parameters of CdTe QDs on their final emission properties. A strong dependence of the final emission wavelength with the reaction time and surface ligands and precursors concentrations was demonstrated. These parameters adjusted synchronously were shown to be very useful for provide ideal synthesis conditions for the preparation of CdTe QDs with desirable emission wavelengths. Moreover, applying the algorithms correctly allows for obtaining information and insights into the growth kinetics of QDs under different synthetic conditions.
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An experimental-theoretical approach is proposed to investigate the size-dependent photobleaching of colloidal semiconductor quantum dots (QDs) excited by a nanosecond pulsed laser. In the experimental background, the ground-state absorption and photoluminescence (PL) spectra of chemically prepared QDs are monitored over an excitation time at distinct laser irradiances. The magnitude of photobleaching in the QD solution is quantified by the decay rate of the PL signal as a function of the excitation time and the laser power. A theoretical spectroscopy model is then used to estimate the particle size distribution (PSD) in colloidal solution from the absorption data generated at different laser powers. The resulting evolution of the PSD of the QD ensemble under irradiation is analyzed in terms of classical crystallization theories dealing with the formation, growth, and dissolution of colloidal particles in a supersaturated medium. The QD response to laser irradiation is also interpreted by a simple mechanical model that correlates the photoinduced hydrostatic strain at the solid/liquid interface and the predicted variation of the mean particle size. The reported experimental and theoretical methods are used to completely elucidate the basic physico-chemical processes responsible for the laser-induced photobleaching kinetics of glutathione-capped CdTe aqueous QDs with very small mean sizes. For this purpose, we synthesized a series of colloidal QD samples with mean particle diameters ranging from 1.95 to 2.68 nm. Our results indicate that a faster photobleaching rate occurs in QD samples with smaller sizes in which particle dissolution under laser irradiation is predominant. On the other hand, the photobleaching rate becomes slower in samples with larger dot sizes, possibly due to the formation of core/shell structures in solution via thermal degradation of thiol ligands either during the chemical synthesis or as a consequence of the subsequent interaction with the excitation laser.
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The modification of endodontic sealers with nanoparticles to confer antimicrobial activity allow greater effect, with interaction at a molecular level. The nanostructured silver vanadate decorated with silver nanoparticles (AgVO3) is a nanomaterial unprecedented in dentistry for this application. This study incorporated the AgVO3 into three endodontic sealers of different compositions and evaluate the cytotoxicity and release of compounds. The groups of commercially available AH Plus, Sealer 26, and Endomethasone N and groups of the same sealers with incorporated AgVO3 (at concentrations 2.5, 5, 10%) were prepared, and extracts of the specimens were obtained for 24 h. The cell viability (cytotoxicity) of human gingival fibroblasts (HGF) was assessed after 24 h, 7 and 14 days. Silver (Ag+) and vanadium (V4+/V5+) ion release was quantified after 24 h by ICP-MS. Data were analyzed by Kruskal-Wallis and Dunn's post-hoc (α = 0.05). The cell viability was inversely proportional to treatment time. The Sealer 26 and Endomethasone N groups were cytotoxic for HGF cells, regardless of the incorporation of the AgVO3 (p > 0.05), and the incorporation reduced cell viability of AH Plus (p < 0.05). The release of ions was proportional to the concentration of AgVO3. AH Plus released more Ag+ ions, and Sealer 26 and Endomethasone N releases more V4+/V5+ ions. In conclusion, it was not possible to confirm the influence of AgVO3 on HGF cell viability to Sealer 26 and Endomethasone N, however, nanomaterial influenced cell-viability to AH Plus, so the commercial sealers can be cytotoxic in synergy with the nanomaterial. The release of Ag+ and V4+/V5+ was proportional to the AgVO3 incorporated.
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Nanopartículas del Metal , Nanoestructuras , Materiales de Obturación del Conducto Radicular , Resinas Epoxi , Fibroblastos , Humanos , Plata , VanadioRESUMEN
STATEMENT OF PROBLEM: Dental porcelain restorations are subject to biological failures related to secondary caries and periodontal disease leading to prosthesis replacement. PURPOSE: The purpose of this in vitro study was to explore the microbiological and mechanical properties of dental porcelain incorporated with different percentages of silver vanadate (ß-AgVO3) through microbiological analysis, roughness tests, and the Vickers microhardness test. MATERIAL AND METHODS: IPS InLine porcelain specimens were made by using a cylindrical Teflon matrix in the dimensions of 8×2 mm. For the control group, the porcelain was manipulated according to the manufacturer's instructions. The groups incorporating the nanomaterial were prepared with 2.5%, 5%, and 10% of ß-AgVO3, which was added proportionally by mass to the porcelain powder. In vitro microbiologic analysis, roughness tests, and the Vickers microhardness test were performed. RESULTS: Against Streptococcus mutans, the control group showed no inhibition halo (0 mm). All groups with AgVO3 showed a zone of inhibition, the highest for the group with 10% (30 mm) and then the groups with 2.5% (9 mm) and 5% (17 mm). For Vickers microhardness, no statistically significant difference (P<.05) was observed between the evaluated groups. The group with 10% of AgVO3 had the highest mean roughness and was statistically different (P<.001) from the other groups. CONCLUSIONS: Adding ß-AgVO3 to dental porcelain demonstrated antimicrobial effectiveness at all concentrations (2.5%, 5%, and 10%), with no effect on Vickers microhardness. The 10% group had higher roughness than the other groups.
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Porcelana Dental , Nanoestructuras , Ensayo de Materiales , Plata , Streptococcus mutans , Propiedades de SuperficieRESUMEN
This work used L-tartaric acid as a model molecule to evaluate how the use of inert and oxidizing atmospheres during pyrolysis affected the physical and optical properties of the resulting carbon dots (CDs). Pyrolysis revealed to be a simple procedure that afforded CDs in a single step, dismissed the addition of organic solvents, and involved only one extraction stage that employed water. By X-ray diffraction a dependency between the structure of the CDs and the atmosphere (oxidizing or inert) used during the pyrolysis was found. Potentiometric titration demonstrated that the CDs were largely soluble in water; it also aided characterization of the various groups that contained sp(3) -hybridized carbon atoms on the surface of the dots. Raman spectroscopy suggested that different amounts of sp(2)- and sp(3)-hybridized carbon atoms emerged on the CDs depending on the pyrolysis atmosphere. In conclusion, the pyrolysis atmosphere influenced the physical properties, such as the composition and the final structure.
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Objective: The aim of this study was to evaluate the roughness, hardness, and color change of pit and fissure sealants of two commercial brands (Fluroshield ™ and Ultraseal XT ™) incorporated with nanostructured silver vanadate nanomaterial decorated with silver nanoparticles (ß-AgVO3) in concentrations (0% - control, 2.5% and 5%). Material and methods: Two commercial brands Fluroshield TM and Ultraseal XT ™ were used to make the samples with dimensions of 6 × 6 × 4 mm. The control group was made according to the manufacturer's instructions and in the groups with the addition of ß-AgVO3, the nanomaterial was added proportionally by mass at percentages of 2.5% and 5%. Roughness properties were evaluated using a 3D Laser Confocal Microscope (n = 10), Knoop microhardness by Microdurometer (n = 10), and color change by Portable Color Spectrophotometer on the CIEDE2000 system (n = 10). Data were evaluated by one-way ANOVA with Bonferroni adjustment and Tukey's mean comparison test at a 5% significance level. Results: Ultraseal XT ™ sealant roughness showed a significant difference between concentrations with the highest mean for the 5% group (P = 0.010). Regarding the hardness, both sealants showed no significant difference between the groups. Fluroshield ™ sealant showed a significant difference in ΔE00 between the control-2.5% 24.93 (3.49) and control-5% 28.41 (2.58). Conclusion: It may be concluded that the incorporation of ß-AgVO3 influenced the increase in roughness for Ultraseal XT ™ pit and fissure sealant, did not interfere with the microhardness of both sealants, and promoted a change in the color of Fluroshield ™ sealant within clinically acceptable limits.
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OBJECTIVES: To incorporate the nanostructured silver vanadate decorated with silver nanoparticles (AgVO3) into denture base materials: heat-cured (HC) and 3D printed (3DP) resins, at concentrations of 2.5 %, 5 %, and 10 %; and to evaluate the antimicrobial activity in two multi-species biofilm: (1) Candida albicans, Candida glabrata, and Streptococcus mutans, (2) Candida albicans, Pseudomonas aeruginosa, and Staphylococcus aureus, and the wettability. METHODS: The AgVO3 was added to the HC powder, and printed samples were coated with 3DP with AgVO3 incorporated. After biofilm formation, the antimicrobial activity was evaluated by colony forming units per milliliter (CFU/mL), metabolic activity, and epifluorescence microscopy. Wettability was assessed by the contact angles with water and artificial saliva. RESULTS: In biofilm (1), HC-5 % and HC-10 % showed activity against S. mutans, HC-10 % against C. glabrata, and HC-10 % and 3DP-10 % had higher CFU/mL of C. albicans. 3DP-5 % had lower metabolic activity than the 3DP control. In biofilm (2), HC-10 % reduced S. aureus and P. aeruginosa, and HC-5 %, 3DP-2.5 %, and 3DP-5 % reduced S. aureus. 3DP incorporated with AgVO3, HC-5 %, and HC-10 % reduced biofilm (2) metabolic activity. 3DP-5 % and 3DP-10 % increased wettability with water and saliva. CONCLUSION: HC-10 % was effective against C. glabrata, S. mutans, P. aeruginosa, and S. aureus, and HC-5 % reduced S. mutans and S. aureus. For 3DP, 2.5 % and 5 % reduced S. aureus. The incorporation of AgVO3 into both resins reduced the metabolic activity of biofilms but had no effect on C. albicans. The wettability of the 3DP with water and saliva increased with the addition of AgVO3. CLINICAL SIGNIFICANCE: The incorporation of silver vanadate into the denture base materials provides antimicrobial efficacy and can prevent the aggravation of oral and systemic diseases. The incorporation of nanomaterials into printed resins is challenging and the coating is an alternative to obtain the inner denture base with antimicrobial effect.
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Biopelículas , Candida albicans , Bases para Dentadura , Nanopartículas del Metal , Pseudomonas aeruginosa , Plata , Staphylococcus aureus , Streptococcus mutans , Vanadatos , Humectabilidad , Biopelículas/efectos de los fármacos , Streptococcus mutans/efectos de los fármacos , Candida albicans/efectos de los fármacos , Staphylococcus aureus/efectos de los fármacos , Vanadatos/farmacología , Vanadatos/química , Pseudomonas aeruginosa/efectos de los fármacos , Plata/farmacología , Plata/química , Bases para Dentadura/microbiología , Nanopartículas del Metal/química , Antiinfecciosos/farmacología , Candida glabrata/efectos de los fármacos , Impresión Tridimensional , Ensayo de Materiales , Humanos , Nanoestructuras , Compuestos de Plata/farmacología , Compuestos de Plata/química , Materiales Dentales/química , Materiales Dentales/farmacologíaRESUMEN
Aim: To develop a ß-AgVO3 gel and evaluate its physicochemical stability and antifungal activity against Candida albicans. Materials & methods: The gel was prepared from the minimum inhibitory concentration (MIC) of ß-AgVO3. The physicochemical stability was evaluated by centrifugation, accelerated stability (AS), storage (St), pH, syringability, viscosity and spreadability tests and antifungal activity by the agar diffusion. Results: The MIC was 62.5 µg/ml. After centrifugation, AS and St gels showed physicochemical stability. Lower viscosity and higher spreadability were observed for the higher ß-AgVO3 concentration and the minimum force for extrusion was similar for all groups. Antifungal effect was observed only for the ß-AgVO3 gel with 20xMIC. Conclusion: The ß-AgVO3 gel showed physicochemical stability and antifungal activity.
We used silver and vanadium to make a gel that can kill fungi in the mouth. We looked at the color of the gel, it's smell and also checked how well it lasted. The gel turned yellow and had no smell and did not spoil for at least 2 months. When we tested the gel against a type of fungus, it worked as well as another medicine called chlorhexidine, which is sold in pharmacies. But when we compared it with another medicine called nystatin, our gel was not as effective in killing the fungus.
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Perovskite nanocrystals hold significant promise for a wide range of applications, including solar cells, LEDs, photocatalysts, humidity and temperature sensors, memory devices, and low-cost photodetectors. Such technological potential stems from their exceptional quantum efficiency and charge carrier conduction capability. Nevertheless, the underlying mechanisms of photoexcitation, such as phase segregation, annealing, and ionic diffusion, remain insufficiently understood. In this context, we harnessed hyperspectral fluorescence microspectroscopy to advance our comprehension of fluorescence enhancement triggered by UV continuous-wave (cw) laser irradiation of CsPbBr3 colloidal nanocrystal thin films. Initially, we explored the kinetics of fluorescence enhancement and observed that its efficiency (φph) correlates with the laser power (P), following the relationship φph = 7.7⟨P⟩0.47±0.02. Subsequently, we estimated the local temperature induced by the laser, utilizing the finite-difference method framework, and calculated the activation energy (Ea) required for fluorescence enhancement to occur. Our findings revealed a very low activation energy, Ea â¼ 9 kJ/mol. Moreover, we mapped the fluorescence photoenhancement by spatial scanning and real-time static mode to determine its microscale length. Below a laser power of 60 µW, the photothermal diffusion length exhibited nearly constant values of approximately (22 ± 5) µm, while a significant increase was observed at higher laser power levels. These results were ascribed to the formation of nanocrystal superclusters within the film, which involves the interparticle spacing reduction, creating the so-called quantum dot solid configuration along with laser-induced annealing for higher laser powers.
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PURPOSE: This study incorporated the nanomaterial, nanostructured silver vanadate decorated with silver nanoparticles (AgVO3), into heat-cured resin (HT) at concentrations of 2.5%, 5%, and 10% and compared the adhesion of multispecies biofilms, surface characteristics, and mechanical properties with conventional heat-cured (HT 0%) and printed resins. MATERIALS AND METHODS: AgVO3 was incorporated in mass into HT powder. A denture base resin was used to obtain printed samples. Adhesion of a multispecies biofilm of Candida albicans, Candida glabrata, and Streptococcus mutans was evaluated by colony-forming units per milliliter (CFU/mL) and metabolic activity. Wettability, roughness, and scanning electron microscopy (SEM) were used to assess the physical characteristics of the surface. The mechanical properties of flexural strength and elastic modulus were tested. RESULTS: HT 10%-AgVO3 showed efficacy against S. mutans; however, it favored C. albicans CFU/mL (P < .05). The printed resin showed a higher metabolically active biofilm than HT 0% (P < .05). There was no difference in wettability or roughness between groups (P > .05). Irregularities on the printed resin surface and pores in HT 5%-AgVO3 were observed by SEM. HT 0% showed the highest flexural strength, and the resins incorporated with AgVO3 had the highest elastic modulus (P < .05). CONCLUSION: The incorporation of 10% AgVO3 into heat-cured resin provided antimicrobial activity against S. mutans in a multispecies biofilm did not affect the roughness or wettability but reduced flexural strength and increased elastic modulus. Printed resin showed higher irregularity, an active biofilm, and lower flexural strength and elastic modulus than heat-cured resin.
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PURPOSE: This in vitro study aimed to investigate the effect of incorporating the semiconductor nanostructured silver vanadate decorated with silver nanoparticles (ß-AgVO3) in a dual-cure resin cement on the degree of conversion (DC), microhardness, roughness, color, adhesion properties before and after artificial aging, and antimicrobial efficacy. MATERIAL AND METHODS: Three test groups were established: control (without ß-AgVO3), with the incorporation of 2.5% and 5% (by weight) of ß-AgVO3 in dual-cure resin cement (Allcem, FGM). The degree of conversion was measured using Fourier transform infrared spectroscopy (FTIR). To evaluate roughness (n = 10), microhardness (n = 10), color (n = 10), and to perform agar disk diffusion (n = 8), disks of 6-mm diameter and 2-mm height were manufactured using the same concentrations. For the color and shear bond strength test (n = 6), orthodontic brackets (Morelli) were used, which were cemented to natural human enamel and evaluated before and after artificial aging via thermocycling at 5°C and 55°C for 1000 cycles. For color measurements, a portable spectrocolorimeter and the CIE-Lab method were used. Data were analyzed using Student's t-test, ANOVA, and Tukey's multiple comparisons with significance set at α = 0.05. RESULTS: Semiconductor incorporation did not influence the cements's DC. The incorporation of 2.5% and 5% of ß-AgVO3 resulted in a significant increase in Knoop microhardness and surface roughness. Significant changes were observed in the color of the specimens when the semiconductor was incorporated. Adhesion after aging remained within the clinically recommended values in all groups, and antimicrobial activity was observed against Staphylococcus aureus, Streptococcus mutans, and Enterococcus faecalis at both concentrations tested. CONCLUSION: It is suggested to incorporate the semiconductor ß-AgVO3 in the dual-cure resin cement at both concentrations. Moreover, the physical-mechanical properties remained satisfactory for the proposed application.
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Antiinfecciosos , Nanopartículas del Metal , Antibacterianos/farmacología , Antiinfecciosos/química , Humanos , Ensayo de Materiales , Cementos de Resina/farmacología , Semiconductores , Plata/química , Plata/farmacología , Propiedades de SuperficieRESUMEN
Halide perovskites are revolutionizing the photovoltaic and optoelectronic fields with outstanding performances obtained in a remarkably short time. However, two major challenges remain: the long-term stability and the Pb content, due to its toxicity. Despite the great effort carried out to substitute the Pb by a less hazardous element, lead-free perovskite still remains more unstable than lead-containing perovskites and presents lower performance as well. In this work, we demonstrate the colloidal preparation of Cs-Pb-Sn-Br nanoparticles (NPs) where Sn is incorporated up to 18.8%. Significantly, we have demonstrated that the partial substitution of Pb by Sn does not produce a deleterious effect in their optical performance in terms of photoluminescence quantum yield (PLQY). We observed for the first time a positive effect in terms of enhancement of PLQY when Sn partially substitutes Pb in a considerable amount (i.e., higher than 5%). PLQYs as high as 73.4% have been obtained with a partial Pb replacement of 7% by Sn. We present a systematic study of the synthesis process in terms of different growth parameters (i.e., precursor concentration, time, and temperature of reaction) and how they influence the Sn incorporation and the PLQY. This high performance and long-term stability is based on a significant stabilization of Sn2+ in the NPs for several months, as determined by XPS analysis, and opens an interesting way to obtain less Pb-containing perovskite NPs with excellent optoelectronic properties.
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We report here on the direct observation of distinct two-photon transition channels in glutathione-capped (GSH) CdTe quantum dots (QDs) in a very strong confinement regime. CdTe-GSH QDs with different average diameters (2.5, 3.0, and 3.3 nm) were synthesized through the one-pot method and their two-photon absorption (2PA) spectrum determined by a femtosecond wavelength-tunable Z-scan. Our results show that the two lower-energy one-photon-allowed excitonic transitions, 1S3/2(h) â 1S(e) and 2S3/2(h) â 1S(e), are also accessed via 2PA. These results were ascribed to the relaxation of the parity selection rules due to the noncentrosymmetric structure of the CdTe QDs (zinc-blended structure), whose magnitude are determined by surface defects and structural irregularities present in CdTe-GSH QDs, in the strong confinement regime.
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OBJECTIVE: This preliminary study aimed to evaluate the antimicrobial activity, flow and radiopacity of endodontic sealers with nanostructured silver vanadate decorated with silver nanoparticles (AgVO3). METHODS: The minimum inhibitory concentration (MIC) of AgVO3 was evaluated against Enterococcus faecalis, Pseudomonas aeruginosa and Escherichia coli. Specimens were prepared from the following endodontic sealers: AH Plus (DENTSPLY DeTrey GmbH, Konstanz, Germany), Sealapex (Sybron Endo, Orange, CA, USA), Sealer 26 (DENTSPLY, Petrópolis, Brazil) and Endofill (DENTSPLY, Petrópolis, Brazil), with concentrations of 0%, 2.5%, 5% and 10% of AgVO3. Agar diffusion was used to evaluate the materials after 48 hours and 7 days (n=6). Flow (n=6) and radiopacity (n=9) were evaluated. The data were analysed by analysis of variance (ANOVA) and the Tukey honestly significant difference (HSD) (α=0.05). RESULTS: The MIC of AgVO3 was 500 µg/mL for E. faecalis and 31.25 µg/mL for P. aeruginosa and E. coli. The AgVO3 did not influence the antimicrobial activity of AH Plus against E. faecalis (P>0.05) but did promote this activity for Sealapex (P<0.01). Moreover, this activity increased for Endofill from 2.5% and for Sealer 26 from 5% (P<0.05). Against P. aeruginosa, only AH Plus and Endofill 10% inhibited zone formation (P<0.01). The antimicrobial activity of Endofill increased from 2.5% against E. coli (P<0.01). Sealapex 5% and 10% (P<0.01), Sealer 26 10% and AH Plus promoted antimicrobial activity against E. coli. An increase in the zone of inhibition occurred between 48 hours and 7 days in the Sealapex 10% and Endofill 5% groups against E. coli. The flow of AH Plus and Endofill decreased with the increase of AgVO3 (P<0.05), and the flow of Sealer 26 and Sealapex was not affected (P>0.05). The radiopacity of AH Plus increased with AgVO3 (P<0.05). Endofill 5% and 10% did not differ from the control Endofill (P>0.05). The incorporation of AgVO3 did not influence the radiopacity of Sealer 26 (P>0.05). The incorporation of 2.5% and 5% AgVO3 reduced the radiopacity of Sealapex (P<0.05). CONCLUSION: Adding AgVO3 may increase the antimicrobial effect of endodontic sealers without major changes in their physicochemical properties.
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The incorporation of antimicrobial agents may influence the mechanical properties of acrylic resins. Thus, the use of these agents only in regions of dental prostheses subject to greater contamination may be an alternative. This study evaluates the effect of thermomechanical fatigue on the bond strength between a conventional and an experimental acrylic resin incorporated with nanostructured silver vanadate decorated with silver nanoparticles (AgVO3). 60 specimens (Ø13mm x 23mm height) in self-curing resin were obtained and divided into groups according to the experimental resin incorporated with AgVO3 (Ø4mm x 6mm height): G1Conventional x Conventional, G2Conventional x 2.5% of AgVO3, G3Conventional x 5% of AgVO3. Ten samples of each group were subjected to bond strength analysis after manufacture, and 10 were previously submitted to 1.200.000 cycles with 98N load and 2Hz/second frequency and alternating baths of 5 ºC, 37ºC and 55 ºC. The fracture area was analyzed. The data were submitted to analysis of variance of two-factors with Bonferroni adjustment for post hoc comparisons (α=0.05) was used. The fatigue did not affect the bond strength (p=0.416), however, there was influence of the AgVO3 concentration on the bond strength between the resins (p=0.013). Mixed failures with adhesive predominance were observed in samples without AgVO3 and cohesive failures in samples with the nanomaterial. The use of AgVO3 can improve or maintain the bond strength between resins with no thermomechanical fatigue influence. (AU).
A incorporação de agentes antimicrobianos pode influenciar nas propriedades mecânicas de resinas acrílicas. Desta forma, o uso destes agentes apenas em regiões das próteses dentárias sujeitas a maior contaminação pode ser uma alternativa. Este estudo avalia o efeito da fadiga termomecânica na resistência de união entre uma resina acrílica convencional e uma experimental incorporada com vanadato de prata nanoestruturado decorado com nanopartículas de prata (AgVO3). Foram obtidos 60 espécimes (Ø13mm x 23mm de altura) em resina autopolimerizável, divididos em grupos de acordo com a resina experimental incorporada com AgVO3 (Ø4mm x 6mm de altura): G1-Convencional x Convencional, G2-Convencional x 2,5% de AgVO3, G3 -Convencional x 5% de AgVO3. Dez amostras de cada grupo foram submetidas à análise de resistência à união após a confecção e 10 foram submetidas previamente a 1.200.000 ciclos com carga de 98 N e frequência de 2Hz/segundo e banhos alternados de 5 ºC, 37 ºC e 55 ºC. A área de fratura foi analisada. Os dados foram submetidos à análise de variância de dois fatores com ajuste de Bonferroni para comparações pos hoc (α = 0,05). A fadiga não afetou a força de união (p=0,416), no entanto, houve influência da concentração de AgVO3 na resistência de união entre as resinas (p=0,013). Falhas mistas com predominância adesiva foram observadas nas amostras sem AgVO3 e falhas coesivas nas amostras contendo o nanomaterial. O uso de AgVO3 pode melhorar ou manter a resistência da união entre as resinas sem influência da fadiga termomecânica.
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The aim of this study was to investigate the influence of accelerated artificial aging (AAA) on the microstructure and mechanical properties of the Filtek Z250, Filtek Supreme, 4 Seasons, Herculite, P60, Tetric Ceram, Charisma and Filtek Z100. composite resins. The composites were characterized by Fourier-transform Infrared spectroscopy (FTIR) and thermal analyses (Differential Scanning Calorimetry - DSC and Thermogravimetry - TG). The microstructure of the materials was examined by scanning electron microscopy. Surface hardness and compressive strength data of the resins were recorded and the mean values were analyzed statistically by ANOVA and Tukey's test (α=0.05). The results showed significant differences among the commercial brands for surface hardness (F=86.74, p<0.0001) and compressive strength (F=40.31, p<0.0001), but AAA did not affect the properties (surface hardness: F=0.39, p=0.53; compressive strength: F=2.82, p=0.09) of any of the composite resins. FTIR, DSC and TG analyses showed that resin polymerization was complete, and there were no differences between the spectra and thermal curve profiles of the materials obtained before and after AAA. TG confirmed the absence of volatile compounds and evidenced good thermal stability up to 200 °C, and similar amounts of residues were found in all resins evaluated before and after AAA. The AAA treatment did not significantly affect resin surface. Therefore, regardless of the resin brand, AAA did not influence the microstructure or the mechanical properties.
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Resinas Compuestas/química , Fuerza Compresiva , Análisis del Estrés Dental , Dureza , Técnicas In Vitro , Ensayo de Materiales , Microscopía Electrónica de Rastreo , Polimerizacion , Dióxido de Silicio/química , Espectroscopía Infrarroja por Transformada de Fourier , Propiedades de Superficie , Termogravimetría , Factores de Tiempo , Rayos Ultravioleta , Circonio/químicaRESUMEN
The aim of this study was to investigate the influence of accelerated artificial aging (AAA) on the microstructure and mechanical properties of the Filtek Z250, Filtek Supreme, 4 Seasons, Herculite, P60, Tetric Ceram, Charisma and Filtek Z100. composite resins. The composites were characterized by Fourier-transform Infrared spectroscopy (FTIR) and thermal analyses (Differential Scanning Calorimetry - DSC and Thermogravimetry - TG). The microstructure of the materials was examined by scanning electron microscopy. Surface hardness and compressive strength data of the resins were recorded and the mean values were analyzed statistically by ANOVA and Tukey's test (α=0.05). The results showed significant differences among the commercial brands for surface hardness (F=86.74, p<0.0001) and compressive strength (F=40.31, p<0.0001), but AAA did not affect the properties (surface hardness: F=0.39, p=0.53; compressive strength: F=2.82, p=0.09) of any of the composite resins. FTIR, DSC and TG analyses showed that resin polymerization was complete, and there were no differences between the spectra and thermal curve profiles of the materials obtained before and after AAA. TG confirmed the absence of volatile compounds and evidenced good thermal stability up to 200 °C, and similar amounts of residues were found in all resins evaluated before and after AAA. The AAA treatment did not significantly affect resin surface. Therefore, regardless of the resin brand, AAA did not influence the microstructure or the mechanical properties.
A influência do sistema de envelhecimento artificial acelerado (EAA) na microestrutura e nas propriedades mecânicas das resinas compostas Z250, Filtek Supreme, 4 Seasons, Herculite, P60, Tetric Ceram, Charisma e Filtek Z100 foi investigada. Os compósitos foram caracterizados por espectroscopia de infravermelho com transformada de Fourier (FTIR) e análises térmicas (calorimetria exploratória diferencial - DSC e termogravimetria - TG). A microestrutura dos materiais foi analisada por microscopia eletrônica de varredura. Os dados de dureza superficial e resistência à compressão foram registados para as resinas e os valores médios foram submetidos ao teste de Kolmogorov-Smirnov (p>0,05), ANOVA e teste de Tukey (α=0,05). Os resultados mostraram diferenças significativas entre as marcas comerciais em termos de dureza (F=86,74, p<0,0001) e resistência à compressão (F=40,31, p<0,0001), mas o EAA não afetou as propriedades (dureza superficial: F=0,39, p=0,53, resistência à compressão: F=2,82, p=0,09) de qualquer uma das resinas. FTIR, DSC e análise de TG revelou que a polimerização da resina foi completa, e não houve diferenças entre os espectros e os perfis de curva térmica dos materiais obtidos, antes e depois de EAA. TG mostrou a ausência de compostos voláteis e evidenciou uma boa estabilidade térmica até 200 °C, e quantidades similares de resíduos foram encontradas em todas as resinas avaliadas, antes e depois de EAA. O tratamento de EAA não afetou significativamente a superfície das resinas. Portanto, independentemente do tipo de resina, o EAA não influenciou a microestrutura e as propriedades mecânicas.