Post-cure heat treatments influence on mechanical and optical properties of resin composites

Abstract This study evaluated the effect of post-cure heat treatment (PCHT) on the Knoop microhardness (KHN), degree of conversion (DC), color changes, and contrast ratio (CR) of four resin composites (RCs): Z100 (3M ESPE), Z350 XT (3M ESPE), Estelite Omega (Tokuyama) and Empress Direct (Ivoclar Vivadent). Specimens (12 × 1 mm) were prepared for each material (n = 10 / group). After curing, samples were subjected to PCHT for 10 min at 100°C or 170°C. Control group was maintained at room temperature (24°C) for the same time. The DC was analyzed by FT-NIR immediately and 24 h after the PCHT (n = 3 / group). KHN was analyzed 24 h after PCHT (n = 10 / group). According to CIEDE2000 (∆E00), color measurements were obtained immediately after curing, five minutes after PCHT, and after seven days of storage in water, coffee, and red wine. Data were analyzed by One and Two-Way ANOVA (p < 0.05). Z100, Z350, and Estelite Omega showed increases in KHN with increased temperature (p < 0.05). PCHT at 100°C and 170°C led to a higher DC of all RCs (p < 0.05). Initially, the PCHT lead to increased ∆E00 values (p < 0.05), which was decreased after immersion in coffee and wine (p < 0.05). Considering the effect of PCHT and staining solutions, lower color changes were observed in the thermally treated specimens (p < 0.05). Taken collectively, the results suggest the PCHT as an economical and practical alternative to enhance direct RC's properties in direct-indirect and indirect restorations.

Resumo Este estudo avaliou o efeito do tratamento térmico pós-cura (PCHT) na microdureza Knoop (KHN), grau de conversão (DC), mudanças de cor e razão de contraste (CR) de quatro compósitos resinosos (RCs): Z100 (3M ESPE ), Z350 XT (3M ESPE), Estelite Omega (Tokuyama) e Empress Direct (Ivoclar Vivadent). Corpos de prova (12 × 1 mm) foram preparadas para cada material (n = 10 / grupo). Após a cura, as amostras foram submetidas ao PCHT por 10 min a 100 ou 170° C. O grupo controle foi mantido à temperatura ambiente (24° C) pelo mesmo tempo. O DC foi analisada por FT-NIR imediatamente e 24 h após a PCHT (n = 3 / grupo). KHN foi analisado 24 h após PCHT (n = 10 / grupo). De acordo com o CIEDE2000 (∆E00), as medidas de cor foram obtidas imediatamente após a cura, cinco minutos após a PCHT e após sete dias de armazenamento em água, café e vinho tinto. Os dados foram analisados por ANOVA de um e dois fatores (P < 0,05). Z100, Z350 XT e Estelite Omega mostraram aumentos no KHN com o aumento da temperatura (P < 0,05). PCHT a 100 ° C e 170 ° C levou a uma maior DC de todos os RCs (P < 0,05). Inicialmente, o PCHT levou ao aumento dos valores de ∆E00 (P < 0,05), que diminuiu após a imersão em café e vinho (P < 0,05). Considerando o efeito de PCHT e soluções de coloração, menores mudanças de cor foram observadas nas amostras tratadas termicamente (P < 0,05). Os resultados sugerem o PCHT como uma alternativa econômica e prática para aumentar as propriedades diretas de compósitos resinosos em restaurações diretas-indiretas e indiretas.

Is prolonged bleaching more harmful to dental enamel than daily dietary and hygienic oral habits?

Abstract The ultrastructural and mechanical properties of enamel surface were evaluated after prolonged bleaching treatments with 10% carbamide peroxide in the presence or absence of orange juice (erosive challenge) and toothbrushing (abrasive challenge). In total, 145 incisor bovine teeth were used in this study. Twenty-five samples were prepared for the ultrastructural evaluations, and 120 samples were prepared for microhardness and roughness tests. These 120 samples were divided into eight experimental groups (n = 15): G1- artificial saliva; G2- abrasion; G3- erosion; G4- dental bleaching; G5- erosion + abrasion; G6- bleaching + abrasion; G7- bleaching + erosion; and G8- bleaching + erosion + abrasion. All groups were tested at T0 (before treatment), T1 (14 days), T2 (21 days), and T3 (28 days). Two-way analysis of variance for repeated measures and the post hoc Sidak tests (p ≤ 0.05) were used. The roughness evaluation demonstrated an increase in damage for all experimental groups with an increase in the time period. For microhardness, the groups exposed to artificial saliva (AS) and abrasive challenge did not show any differences at any time points, while the other groups showed a decrease in microhardness from T0 to T3. Ultrastructural evaluation showed different surface alterations in response to the treatments. Despite prolonged bleaching periods, the procedure caused lesser enamel surface alterations than exposure to orange juice alone or in combination with brushing.

CO2 laser for dental alumina ceramic framework welding / O laser de CO2 para a soldagem de infraestruturas cerâmicas de alumina

Objective: Despite the increase of all-ceramic prosthesis in dental practice there is no evidence of the possibility of welding these structures if necessary. The objective of this study was to use CO2 laser (λ = 10.6 µm) as a welding agent to fuse dental polycrystalline alumina ceramic. Methods: Ceramic blocks of pre-sintered alumina were sectioned into 20 bars (10.0 x 1.5 x 1.5 mm) and sintered to the final cross section dimension of 1.2 x 1.2mm. The bars were adapted to an LHPG (Laser Heated Pedestal Growth) system device where the bars could be fixed in pairs and have their ends irradiated with CO2 laser to fusion. The ring-shaped laser beam (300 µm thickness) was directed with the aid of mirrors to reach samples' ends. The laser was continuously applied (40 W nominal power, 5 seconds). After welding, the samples were analyzed in stereomicroscope and SEM. A diffraction analysis was carried out with one sample. Results: CO2 laser was able to fuse the ceramic bars, but some of them showed some shape distortion in the fusion zone. The aspect of the fused alumina differed in color and translucency from the original sintered material. SEM evidenced the presence of porosity and voids in the center of the fusion zone. X-ray diffraction pointed to a reduction in crystallite size by two to four times in the welded region of samples. Conclusions: This study points to CO2 laser as a possible welding agent to polycrystalline alumina dental ceramic. Porosity observed in the molten zone gives cause for concern regarding weld resistance. (AU)

Objetivo: Apesar do aumento no número de próteses totalmente cerâmicas na prática clínica, não há evidência da possibilidade de se soldar essas estruturas se necessário. Este estudo testou o laser de CO2 (λ=10.6 µm) como um agente de solda para estruturas cerâmicas de alumina policristalina. Métodos: Blocos cerâmicos de alumina pré-sinterizada foram seccionados na forma de barras (10,0 x 1,5 x 1,5 mm) e sinterizados na dimensão final de 1,2 x 1,2 mm. As barras foram adaptadas a um sistema de crescimento de fibras cerâmicas (LHPG ­ Laser Heated Pedestal Growth) onde as barras foram fixadas em pares e tiveram suas extremidades irradiadas com laser de CO2 até a sua fusão. O feixe de laser foi direcionado com a ajuda de espelhos para atingir as extremidades das barras. O laser foi aplicado de forma contínua (40 W de potência nominal, 5 segundos). Depois da solda, os espécimes foram analisados em estereomicroscopia e MEV. Teste de difração foi conduzido com um espécime. Resutados: O laser de CO2 foi capaz de fundir as barras cerâmicas, mas algumas delas mostraram uma distorção da forma na zona de fusão. O aspecto da alumina soldada diferiu em cor e translucidez do material original. O MEV evidenciou a presença de porosidade no centro da zona de fusão. A difração por raio-x apontou para uma redução no tamanho dos cristalitos de duas a quatro vezes na região da solda. Conclusões: Esse estudo mostrou ser possível usar o laser de CO2 como um agente de solda para uma cerâmica policristalina de alumina. A porosidade observada na zona de fusão traz preocupação quanto à resistência da solda. (AU)

Influence of the Extended Use of Desensitizing Toothpastes on Dentin Bonding, Microhardness and Roughness

Abstract The aim of this study was to evaluate the influence of an extended use of desensitizing toothpastes (DTs) on dentin bonding, microhardness and roughness. One hundred and twenty bovine incisor teeth were randomly divided into four groups: G1, distilled water (WATER); G2, Colgate Total 12 (CT12); G3, Colgate Sensitive Pro-Relief (CSPR); and G4, Sensodyne Repair ?αμπ; Protect (SRP). Dentin surfaces were etched with 17% EDTA and 2 years of simulated tooth brushing (20,000 cycles) was performed on their surfaces. Knoop microhardness, surface roughness and scanning electron microscopy (SEM) were performed before and after the simulated tooth brushing. For microshear bonding test, a 2-step self-etching adhesive system (Clearfil SE Bond) was used and 0.8 mm diameter composite resin (Filtek Z350 XT) cylinders were built. Microshear test was performed with an orthodontic wire and with a crosshead speed of 0.5 mm/min. The data were analyzed for: 1) bond strength (one-way ANOVA), 2) microhardness intra-group (Student's test) and inter-group (one-way ANOVA/Tukey's test) comparisons, 3) roughness intra-group (Student's test/Wilcoxon's test) and inter-group (Kruskal-Wallis/Student-Newman-Keuls test) comparisons. The extended use of both dentifrices (conventional and for sensitive teeth) did not affect the bond strength and produced a significant increase in microhardness and roughness of the dentin, except for the microhardness of the SRP group. The simulated tooth brushing technique with water produced an increase in roughness, without reducing significantly the dentin microhardness.

Resumo O objetivo deste estudo foi avaliar a influência do uso prolongado de dentifrícios dessensibilizantes (DTs) na adesão, microdureza e rugosidade da dentina. Cento e vinte dentes incisivos bovinos foram divididos aleatoriamente em quatro grupos: G1, água destilada (WATER); G2, Colgate Total 12 (CT12); G3, Colgate Sensitive Pro-alívio (CSPR); e G4, Sensodyne Repair ?αμπ; Protect (SRP). As superfícies dentinárias foram condicionadas com EDTA a 17% e foram realizados 2 anos de escovação dental simulada (20.000 ciclos) em suas superfícies. A microdureza Knoop, rugosidade de superfície e microscopia eletrônica de varredura (MEV) foram realizadas antes e após escovação dental simulada. Para o teste de adesão por microcisalhamento, foi aplicado um sistema adesivo auto condicionante de 2 passos (Clearfil SE Bond) e foram construídos cilindros de resina composta (Filtek Z350 XT) de 0,8 mm de diâmetro. O teste de microcisalhamento foi realizado com um fio ortodôntico e com velocidade de 0,5mm/min. Os dados foram analisados para: 1) resistência de união (ANOVA 1 fator), 2) comparações de microdureza intra grupo (teste t de Student) e inter grupo (ANOVA 1 fator / teste de Tukey), 3) comparações de rugosidade intra grupo (teste t de Student / teste de Wilcoxon) e inter grupo (Kruskal Wallis / teste de Student-Newman-Keuls). O uso prolongado de ambos dentifrícios (convencional e para dentes sensíveis) não interferiu na resistência de união e produziu um aumento significativo na microdureza e rugosidade da dentina, exceto para a microdureza do grupo SRP. A técnica de escovação dental simulada com água promoveu aumento na rugosidade, sem reduzir significativamente a microdureza da dentina.

Effect of Glaze Cooling Rate on Mechanical Properties of Conventional and Pressed Porcelain on Zirconia

Abstract The aim of this study was to characterize a conventional and a pressed porcelain for zirconia core as to biaxial flexural strength (BFS), apparent fracture toughness (FT) and microstructure composition, and to investigate the effect of glaze cooling rate on the BFS of the zirconia/porcelain bilayers. Monolayers of conventional porcelain Vita VM9 and pressed porcelain Vita PM9 (n=15) (12 mm diameter x 1.2 mm thick) were prepared for the BFS test (MPa). Apparent fracture toughness (MPa.m1/2) was measured by indentation technique (n=15). t-Student test was performed for statistical analysis. Scanning electron microscopy and x-ray diffraction were used to analyze the porcelain's microstructure. For the BFS of bilayers, zirconia discs (12 mm diameter x 1 mm thick) (Vita In-Ceram YZ) were veneered with the two porcelains (1 mm thick). After the glaze firing simulation, the specimens were submitted to fast or slow cooling (n=15). Apparent fracture toughness (MPa.m1/2) was measured on the porcelain surface of bilayers (n=15) and residual stress was calculated. Two-way ANOVA (porcelain and cooling method) was used for the bilayer analysis (a=0.05). Vita PM9 monolayer exhibited significantly higher BFS (p<0.01), but there was no significant difference (p=0.41) in the FT between the porcelains. For bilayer specimens, the two-way ANOVA for BFS was significant for the porcelain variable only (p<0.01) better for Vita PM9/zirconia. Two-way ANOVA for the FT for the bilayers was not significant for any variable. All groups showed compressive residual stresses. The pressed porcelain seems to be mechanically more effective for zirconia veneering.

Resumo Este estudo teve como objetivo caracterizar uma porcelana convencional e uma prensada indicadas para infraestrutura de zircônia em termos de resistência à flexão biaxial (RFB), tenacidade à fratura aparente (TF) e composição microestrutural, e investigar o efeito da taxa de resfriamento do ciclo de glaze na RFB de espécimes bicamada de zircônia/porcelana. Espécimes monocamada de porcelana convencional Vita VM9 e porcelana prensada Vita PM9 (n=15) (12 mm de diâmetro x 1,2 mm de espessura) foram preparados para o ensaio de RFB (MPa). Tenacidade à fratura aparente (MPa.m1/2) foi mensurada pela técnica da indentação (n=15). O teste de t-Student foi aplicado para as análises estatísticas. Microscopia eletrônica de varredura e difração de raios-X foram utilizadas para análise microestrutural da porcelana. Para o ensaio de RFB nos bicamadas, discos de zircônia (12 mm de diâmetro x 1 mm de espessura) (Vita In-Ceram YZ) foram recobertos com as duas porcelanas (1 mm de espessura). Após a simulação da queima de glaze, os espécimes foram submetidos ao método de resfriamento rápido ou lento (n=15). A tenacidade à fratura aparente (MPa.m1/2) foi mensurado na superfície da porcelana dos bicamadas (n=15) e o estresse residual foi calculado. Foi utilizado ANOVA a dois fatores (porcelana e método de resfriamento) para análise estatística dos espécimes bicamada (a=0,05). Monocamadas de Vita PM9 exibiram valores de resistência à flexão biaxial significativamente maiores (p<0,01), mas não houve diferença estatística (p=0,41) em relação à TF entre as porcelanas. Para os espécimes bicamada, ANOVA a dois fatores para RFB foi significante apenas para a variável porcelana (p<0,01), com superioridade para Vita PM9/zircônia. ANOVA a dois fatores para TF dos espécimes bicamadas não apresentou significância para nenhuma variável. Todos os grupos apresentaram estresse residual de compressão. Porcelanas prensadas parecem ser mecanicamente mais efetivas para recobrimento de zircônia.

Influence of prolonged use of desensitizing dentifrices on dentin bond strength of self-etching adhesive system / Influencia del uso prolongado de pasta dentífrica desensibilizante en la fuerza de unión de la dentina de un sistema adhesivo autocondicionante

Dentin hypersensitivity is a relatively common clinical condition, which affects a large part of the world's population. The objective of this study was to evaluate the influence of previous and prolonged treatment with desensitizing dentifrices (DD) on bond strength to dentin, promoted by a self-etching adhesive system. Seventy non-carious bovine incisors were used, and divided into five groups (n= 14), according to the desensitizing toothpaste used, such as, G1: distilled water (WATER) (control); G2: Colgate Total 12 (CT12) (control); G3: Colgate Sensitive Pro-Relief (CSPR); G4: Sensodyne Rapid Relief (SRR); G5: Sensodyne Repair & Protect (SRP). Teeth had their buccal surfaces flattened until the exposure of dentin, and fragments of 4x4x2 mm were obtained. Fragments were included in polyvinyl chloride (PVC) cylinders and exposed to 17 % EDTA for 1 min. Subsequently, specimens were submitted to 20 000 cycles of simulated dental toothbrushing. After 24 h in artificial saliva, specimens were hybridized (Clearfil SE Bond ­ Kuraray), as well as resin composite cylinders built on dentin surfaces. Samples were stored in distilled water, at 37 C for 24 h, and the shear bond strength was determined. The highest bond strength (MPa) value was seen in CT12 group (4.39), and the lowest one in CSPR group (3.34). Data were statistically analyzed by 1-way ANOVA (ð= 0.05), and results showed that there were no significant differences (p= 0.5986) considering the DD factor. The predominant fracture pattern was cohesive on dentin. The previous and prolonged use of different DD did not affect dentin bond strength promoted by a self-etching adhesive system.

La hipersensibilidad dentinaria es una condición clínica relativamente común, que afecta a una gran parte de la población mundial. El objetivo fue evaluar la influencia del tratamiento previo y prolongado con dentífricos desensibilizantes (DD) en fuerza de adhesión a la dentina, que promueve un sistema adhesivo de autograbado. Se utilizaron 70 incisivos bovinos no cariados, y se dividieron en cinco grupos (n= 14), de acuerdo con la pasta de dientes desensibilizante utilizada: G1: agua destilada (agua) (control), G2: Colgate Total 12 (CT12) (control), G3: Colgate Sensitive Pro-Alivio (CSPR), G4: Sensodyne Rápido Alivio (SRR) y G5: Sensodyne Repair & Protect (SRP). Los dientes tenían sus superficies bucales aplanadas hasta la exposición de la dentina, y se obtuvieron fragmentos de 4x4x2 mm. Los fragmentos se incluyeron en cilindros de cloruro de polivinilo y se expusieron a 17 % de EDTA durante un 1 min. Después, las muestras se sometieron a 20 000 ciclos de cepillado dental simulado. Después de 24 h en saliva artificial, las muestras se hibridaron (Clearfil SE Bond - Kuraray), y cilindros de resina compuesta fueron construidos sobre superficies de dentina. Las muestras se almacenaron en agua destilada, a 37 °C durante 24 h y luego se determinó la resistencia al cizallamiento. El mayor valor de resistencia a la unión (MPa) se observó en el grupo CT12 (4,39), y el menor en el grupo CSPR (3,34). Los datos fueron analizados estadísticamente mediante ANOVA de un factor 1 (ð= 0,05), y los resultados no mostraron diferencias significativas (p= 0,5986) teniendo en cuenta el factor de los DD. El patrón de fractura predominante sobre la dentina fue el cohesivo. El uso previo y prolongado de diferente DD no afectó resistencia de unión a la dentina promovido por un sistema adhesivo de autograbado.

Evaluation of the mechanical properties of acetic-cure silicone with the addition of magnesium silicate / Avaliação das propriedades mecânicas de silicone de cura acética, com a adição de silicato de magnésio

Current study evaluates the mechanical properties (tensile and tear strength) of an acetic- cure silicone with the addition of 10 or 20% vol. magnesium silicate. Magnesium silicate was added to the silicone at concentrations of 10 (MS-10) and 20% (MS-20) volume, followed by the analysis of tensile strength, maximal elongation during tensile and tear strength. Results were compared to control group of silicone without additives (CG). Mean rates were determined and compared by analysis of variance and Tukey's test (p < 0.05). Control group had the greatest elongation when subjected to tensile strength (650%), whereas the MS-10 group statistically showed a better tensile strength (8.8 MPa) when compared to CG (7.5 MPa) and MS -20 (7.5 MPa) groups. Both magnesium silicate groups exhibited statistically similar tear strength, whereas MS-20 group demonstrated statistically greater tear strength. The addition of 10% magnesium silicate increased tensile strength, but tear strength and elongation were similar to control. The addition of 20% magnesium silicate did not affect tensile but increased tear strength.

O objetivo deste estudo foi avaliar as propriedades mecânicas (resistência à tração e ao rasgamento) de um silicone de cura acética com adição de 10 ou 20% em volume de silicato de magnésio. O silicato de magnésio foi adicionado ao silicone em concentrações de 10 (MS-10) e 20% (MS-20), em volume, avaliado por análise de resistência à tração, deformação máxima em tração e resistência ao rasgamento. Os resultados foram comparados com um grupo de controle sem aditivos de silicone (GC). Os valores médios foram determinados e comparados através de análise de variância e teste de Tukey (p < 0,05). O grupo de controle apresentou o maior alongamento quando submetido à tensão (650%). O grupo MS-10 exibiu estatisticamente melhor resistência à tração (8,8 MPa) em relação ao GC (7,5 MPa) e MS-20 (7,5 MPa) grupos. Ambos os grupos de silicato de magnésio exibiram médias de resistência ao rasgamento estatisticamente semelhantes, enquanto que o grupo de EM-20 demonstrou estatisticamente maior resistência ao rasgamento em comparação com o grupo de controle. A adição de 10% de silicato de magnésio em volume propiciou maiores valores de resistência ao rasgamento e resistência à tração. A adição de 20% de silicato de magnésio não afetou a resistência à tração, mas produziu aumento na resistência ao rasgamento.

Bond strenght of zirconia submitted to different surface treatments

To evaluate the shear bond strength of a recent adhesive system used in the cementation of zirconia.Material and Methods:Overall, 72 zirconia specimens (Zirconzhan) were divided and randomized into 3 groups according to the type of surface treatment: G1 no treatment + adhesive system; G2 blasted with aluminum oxide + adhesive system and G3 tribochemical treatment (Rocatec Plus) + adhesive system. Half of each group (n = 12) had bond strength evaluated on two occasions: 24 hours after cementation, kept stored in distilled water at 37 ° C without thermal cycling, and after thermal cycling (5000 cycles, 5°C-55°C). Data were analyzed by ANOVA with Tukey's post-test (α≤0.05).Results:At first moment, G1 and G3 showed higher bond strength (8.64 ± 3.43 MPa and 6.55 ± 2.27 MPa) compared to G2, with no statistically significant difference between them. After thermal cycling, G3 showed higher bond strength (7.70 ± 1.82 MPa).Conclusion:Initially, only the adhesive system promoted higher bond strength, but after thermal cycling,bond strength decreased. The best treatment to promote high bond strength to zirconia is to associate tribochemical treatment with the adhesive system; most failures observed after thermal cycling were mixed and cohesive, showing a mechanical imbrication of the adhesive system, suggesting that there is no chemical bond; and the surface of the group with greater bond strength after thermal cycling showed more surface irregularities compared to the other groups...

Sintering dental porcelain with CO2 laser: porosity and mechanical characterization / Sinterização de porcelanas dentárias com o laser de CO2: porosidade e caracterização mecânica

Objective: This study investigated CO2 laser sintering of dental porcelain as an alternative to a conventional furnace by means of porosity, density, fracture toughness and microhardness tests. Methods: Two commercial veneering porcelains were chosen for this study: VM7 and VM9 (VITA Zahnfabrik). 25 porcelain green discs (4.1 mm dia. x 2.4 mm) of each commercial brand were confectioned and divided into 5 groups: a control group (oven-glazed specimens) and 4 groups of specimens sintered by continuous CO2 laser (Coherent, USA – 35 W e λ= 10.6 μm) with different fluences: 6000, 6900, 12000 and 13800 J/cm2. After sintering, the discs had one of their surfaces mirror polished until the final dimension of 3.5 mm x 2.0 mm was achieved. The amount of superficial pores (%) was assessed by the Image J software through images obtained from an optical microscope (Shimadzu - 100x). Apparent density was measured by the Archimedean’s method. Microhardness and fracture toughness (Indentation Fracture - IF) were determined with a Vickers indenter (Shimadzu). Results: Porosity ranged between 4.0 to 5.9% for the irradiated specimens; the control group had 6.0 and 4.7% of porosity for porcelain VM7 and VM9, respectively. The density of the VM7 porcelain irradiated in 13800 J/cm2 fluence was significantly higher than the control group. The microhardness and fracture toughness of the irradiated specimens were similar to the control. The indentation marks of some irradiated groups were not possible to achieve because the surface cracked during the test. Conclusions: Porcelain sintered with CO2 laser in studied fluences produced a material with superficial porosity similar to that obtained in a conventional oven. Depending on the commercial brand and/or the laser fluence, the irradiated specimens presented a density, fracture toughness and microhardness results that differed from the control group.

Objetivo: Este estudo testou o laser de CO2 como um agente de sinterização de porcelanas dentárias e o comparou ao forno convencional por meio das seguintes caracterizações: porosidade, densidade, tenacidade à fratura e microdureza. Materiais e métodos: Duas porcelanas comerciais foram escolhidas para o estudo: VM7 e VM9 (VITA Zahnfabrik). 25 discos (4,1 mm dia. x 2,4 mm) de cada porcelana foram confeccionados e divididos em 5 grupos: 1 grupo controle (espécimes sinterizados no forno) e 4 grupos de espécimes sinterizados pelo laser de CO2 de forma contínua (Coherent, USA – 35 W e λ= 10,6 μm) em diferentes fluências: 6000, 6900, 12000 e 13800 J/cm2. Após a sinterização, os discos tiveram uma de suas faces polidas. A dimensão final dos espécimes foi de 3,5 x 2,0 mm. A contagem de poros superficiais (%) foi feita pelo programa Image J (domínio público) através de imagens obtidas em um microscópio óptico (Shimadzu - 100x). A densidade aparente foi medida por Arquimedes. A microdureza e a tenacidade à fratura (método IF - Indentation Fracture) foram determinadas por um indentador Vickers (Shimadzu). Resultados: A porosidade variou entre 4,0 e 5,9% para os espécimes irradiados; o grupo controle apresentou a porosidade de 6,0 e 4,7% para o grupo controle das porcelanas VM7 e VM9, respectivamente. A densidade da porcelana VM7 irradiada na fluência de 13800 J/cm2 foi significantemente maior do que a observada no grupo controle. A microdureza e a tenacidade à fratura dos espécimes irradiados foram similares ao grupo controle, porém em alguns grupos não foi possível se obter as marcas de indentação devido ao trincamento da superfície, o que inviabilizou o teste. Conclusões: A sinterização com o laser de CO2 produziu uma porcelana com porosidade superficial semelhante àquela obtida em forno convencional. Dependendo da marca comercial ou da fluência do laser, os resultados de densidade, tenacidade à fratura e microdureza diferiram dos do grupo controle

Conjugados cerâmicos odontológicos reforçados por fibras cristalinas obtidas por fusão a laser / Dental ceramics reinforced with crystaline fibers obtained by laser meting technique

Esse trabalho foi dividido em duas etapas: o objetivo de primeira foi o de aperfeiçoar e obtenção de fibras de com 5% em peso de excesso de alumina em relação a composição eutética, em velocidade de crescimento de 48 a 228 mm/h, para a produção de fibras de diâmetro inferior a 0,5mm. A segunda etapa consistiu em desenvolver e caracterizar os novos conjugados cerâmico monolíticos e bilaminados, por meio da avaliação da densidade (p), módulo de elasticidade (E), coeficiente de expansão térmica linear (CETL), resistência à flexão (o.) e análise por microscopia eletrônica de varredura da interface fibra-matriz cerâmica e superfície de fratura. Os conjugados monolíticos foram produzidos pela combinação de 7,5%vol de fibras cerâmicas de AI20~GdAI03, obtidas durante a primeira fase, com uma porcelana (VM7

Conclusões: foi possível obter fibras de AbO;JGdAI03, com 5% em peso de excesso de alumina em relação a composição eutética, pela técnica de Laser Heated Pedestal Growth (LHPG) com diâmetro médio de 0,45 mm. Foi observado espaçamento médio entre as fases de 0,21 um, com as fases alinhadas na direção do crescimento, em fibras obtidas com elevadas taxas de puxamento (168 e 228 mm/h). Esses grupos mostraram resistência à flexão média superior às obtidas com as demais taxas de puxamento (48 a 96 mm/h); O reforço com 7,5% em volume de fibras longas unidirecionais de AbO;JGdAI03 foi suficiente para aumentar significativamente a resistência à flexão de conjugados cerâmicos monolíticos e bilaminados, exceto para o bilaminado que associa cerâmica infiltrada com vidro e porcelana. De modo geral, as propriedades de densidade, módulo de elasticidade e o coeficiente de expansão térmica linear não apresentaram alterações significativas com a adição de fibras para reforço nos conjugados. A interface fibra-cerâmica apresentou-se íntegra sem a presença de fendas. A análise fractográfica indicou a origem da fratura nas superfícies dos corpos-de-prova que estavam sob tração no ensaio de flexão.

This work was divided in two parts: the objective of the first part was to improve the technique to manufacture AI20:JGdAI03 fibers with 5% in weight of excess alumina in relation to the eutectic composition, using growth speeds varying from 48 to 228 mm/h in order to obtain fibers with diameter of 0.5 mm or less. The second part of the work comprised the development and haracterization of new ceramic composites in two configurations (monolayer and bilayer) by means of the determination of: density, elastic modulus, coefficient of thermal expansion, flexural strength, and quality of the fiber/matrix interface by scanning electron microscopy.Monolithic specimens were produced by combining 7.5 vo% of AI20:JGdAI03 fibers (obtained during the first round of the study) either with porcelain VM7 (Vita Zahnfabrik, Alemanha) or with a glass-infiltrated alumina (InCeram, Vita Zahnfabrik, Alemanha). The bilayers were obtained by adding the AI20:JGdAI03 fibers to porcelain VM7 which as combined with two different core aterial: glass-infiltrated alumina processed by slip-cast (InCeram, Vita Zahnfabrik, Alemanha) or alumina polycristal processed by CAD-CAM (InCeram AL, Vita Zahnfabrik, Alemanha). Results of Part 1: the fibers obtained had 0.45 mm in diameter and flexural strength varying from ,260.0 to 2,390.0 MPa. Spacing among phases varied from 0.21 to 0.68 11m. The lowest spacing values and highest flexural strength were obtained by fibers pulled at 168 e 226 mm/h. Results of Part 2: mechanical characterization of the composites produced showed that the fibers were apable of reinforcing both the monotithic and bilayered specimens, as these had significantly higher flexural strength compared to their respective controls.

The only exception to that was the bilayer in which the glass-infiltrated alumina was combined with the fiber-reinforced porcelain. The fiber/matrix interface was free of defects and the fractographic analysis indicated that the origin of the fracture was located on the tensile surface of the specimen and the crack propagated through the fibers. Conclusion: The AI20JGdAI03 fibers with 5% in weight of excess alumina in relation to the eutectic composition showed mean diameter of 0.45 mm and the mean spacing between phases was 0.2 um, These phases were aligned in the same direction of the fiber growth when high pulling speeds were used (168 e 228 mm/h). These experimentalgroups showed higher flexural strength compared to those in which other pulling speeds were used. The monolithic and bilayered composites reinforced with 7.5 vol% of unidirectional long fibers showed higher flexural strength compared to their respective control groups, except for the bilayer in which the glass-infiltrated composite was associated with the fiber-reinforced porcelain. The fiber/ceramic interface was shown to be free of defects or gaps.

Effect of different polishing systems on the surface roughness of microhybrid composites

The use of composite resins in dentistry is well accepted for restoring anterior and posterior teeth. Many polishing protocols have been evaluated for their effect on the surface roughness of restorative materials. This study compared the effect of different polishing systems on the surface roughness of microhybrid composites. Thirty-six specimens were prepared for each composite $#91;Charisma® (Heraeus Kulzer), Fill Magic® (Vigodent), TPH Spectrum® (Dentsply), Z100® (3M/ESPE) and Z250® (3M/ESPE)] and submitted to surface treatment with Enhance® and PoGo® (Dentsply) points, sequential Sof-Lex XT® aluminum oxide disks (3M/ESPE), and felt disks (TDV) combined with Excel® diamond polishing paste (TDV). Average surface roughness (Ra) was measured with a mechanical roughness tester. The data were analyzed by two-way ANOVA with repetition of the factorial design and the Tukey-Kramer test (p<0.01). The F-test result for treatments and resins was high (p<0.0001 for both), indicating that the effect of the treatment applied to the specimen surface and the effect of the type of resin on surface roughness was highly significant. Regarding the interaction between polishing system and type of resin used, a p value of 0.0002 was obtained, indicating a statistically significant difference. A Ra of 1.3663 was obtained for the Sof-Lex/TPH Spectrum interaction. In contrast, the Ra for the felt disk+paste/Z250 interactions was 0.1846. In conclusion, Sof-Lex polishing system produced a higher surface roughness on TPH Spectrum resin when compared to the other interactions.

Heat treatment of a direct composite resin: influence on flexural strength

The purpose of this study was to evaluate the flexural strength of a direct composite, for indirect application, that received heat treatment, with or without investment. One indirect composite was used for comparison. For determination of the heat treatment temperature, thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) were performed, considering the initial weight loss temperature and glass transition temperature (Tg). Then, after photoactivation (600 mW/cm©÷ - 40 s), the specimens (10 x 2 x 2 mm) were heat-treated following these conditions: 170¨¬C for 5, 10 or 15 min, embedded or not embedded in investment. Flexural strength was assessed as a means to evaluate the influence of different heat treatment periods and investment embedding on mechanical properties. The data were analyzed by ANOVA and Tukey's test (¥á = 0.05). TGA showed an initial weight loss temperature of 180¨¬C and DSC showed a Tg value of 157¡ÆC. Heat treatment was conducted in an oven (Flli Manfredi, Italy), after 37¡ÆC storage for 48 h. Flexural strength was evaluated after 120 h at 37¡ÆC storage. The results showed that different periods and investment embedding presented similar statistical values. Nevertheless, the direct composite resin with treatments presented higher values (178.7 MPa) compared to the indirect composite resin (146.0 MPa) and the same direct composite submitted to photoactivation only (151.7 MPa). Within the limitations of this study, it could be concluded that the heat treatment increased the flexural strength of the direct composite studied, leading to higher mechanical strength compared to the indirect composite.

Effect of light-activation methods and water storage on the flexural strength of two composite resins and a compomer

O presente estudo analisou a resistência à flexão de três compósitos recomendados para restaurações estéticas diretas: um compósito poliácido-modificado (Dyract AP), uma resina composta unimodal (Filtek Z250) e uma resina composta híbrida (Point 4). Os fatores de variação, além do tipo de compósito, foram o método de fotoativação e o período de armazenagem em água. Os materiais foram fotoativados continuamente por 40 s (500 mW/cm²) ou com intensidade de luz crescente (0-800 mW/cm² por 10 s seguidos de 30 s a 800 mW/cm²). Os períodos de armazenagem foram de 24 horas ou 30 dias em água destilada a 37°C. Os dados foram submetidos à análise de variância e ao teste de Tukey para comparações múltiplas (a = 0,05). A resina composta Z250 apresentou a maior média de resistência à flexão (166,74 MPa) e a Dyract AP, a menor (129,76 MPa). A armazenagem por 30 dias diminuiu a resistência à flexão para o método de fotoativação crescente (24 h: 156,64 MPa; 30 dias: 135,58 MPa). O método de fotoativação isoladamente não conduziu a diferentes valores de resistência à flexão.