Influence of the Calcium Orthophosphate (CaP): Glass Ratio and CaP Functionalization on the Degree of Conversion and Mechanical Properties of Experimental Dimethacrylate-Based Composites

2021 ◽  
Author(s):  
Amanda L. Campos ◽  
Bruna M. Fronza ◽  
Marcela C. Rodrigues ◽  
Marina D. S. Chiari ◽  
Roberto Braga
2018 ◽  
Vol 53 (7) ◽  
pp. 981-990
Author(s):  
Fernanda P Ritto ◽  
Eduardo Moreira da Silva ◽  
Hélio Rodrigues Sampaio-Filho ◽  
Raimundo A Lacerda ◽  
Márcio AP Borges ◽  
...  

The aim of this study was to characterize organic and disperse phase of a microhybrid (Mh – Filtek Z250) and a nanofilled (Nf – Filtek Z350) dental composite and analyze the influence of two LCUs (QHT-quartz-halogen tungsten and LED – light-emitting diode) on its physical–mechanical properties (degree of conversion, polymerization shrinkage, Vickers hardness and diametral tensile strength). Surface morphology was studied by scanning electron microscopy. The disperse phase content was measured using thermogravimetric analysis (TGA) and the organic fractions were qualitatively analyzed by nuclear magnetic resonance spectroscopy. Physical–mechanical properties were analyzed varying dental composite and LCU: Mh-QHT, Nf-QHT, Mh-LED and Nf-LED. The degree of conversion was evaluated using Raman spectrophotometry and polymerization shrinkage was measured by water picnometry. Mechanical behavior was analyzed by Vickers microhardness and diametral tensile testing. Scanning electron microscopy analysis showed similar microstructure of the materials mainly composed with different-sized particles dispersed within methacrylate matrix. Thermogravimetric analysis shows 80.13% of inorganic fraction for microhybrid composite and 75.29% for nanofilled. Nuclear magnetic resonance analysis showed similar organic structure for composites and did not show the presence of the monomer TEGDMA. Different light sources did not influence the tested properties, but considering different composites, nanofilled showed the highest degree of conversion (Gr 2:77%, Gr 4: 79.4%). The study shows that when the optimum radiant exposure (24 J/cm2) was used for polymerization of composites, regardless of the polymerization source, the properties of these resin materials showed satisfactory and similar results in relation to the conversion of polymers, polymerization shrinkage and mechanical behavior.


Author(s):  
Leila Perea-Lowery ◽  
Mona Gibreel ◽  
Pekka K. Vallittu ◽  
Lippo Lassila

Materials ◽  
2020 ◽  
Vol 13 (12) ◽  
pp. 2704
Author(s):  
Krzysztof Pałka ◽  
Joanna Kleczewska ◽  
Emil Sasimowski ◽  
Anna Belcarz ◽  
Agata Przekora

There are many methods widely applied in the engineering of biomaterials to improve the mechanical properties of the dental composites. The aim of this study was to assess the effect of modification of dental composites with liquid rubber on their mechanical properties, degree of conversion, viscosity, and cytotoxicity. Both flow and packable composite consisted of a mixture of Bis-GMA, TEGDMA, UDMA, and EBADMA resins reinforced with 60 and 78 wt.% ceramic filler, respectively. It was demonstrated that liquid rubber addition significantly increased the fracture toughness by 9% for flow type and 8% for condensable composite. The influence of liquid rubber on flexural strength was not statistically significant. The addition of the toughening agent significantly reduced Young’s modulus by 7% and 9%, respectively, while increasing deformation at breakage. Scanning electron microscopy (SEM) observations allowed to determine the mechanisms of toughening the composites reinforced with ceramic particles. These mechanisms included bridging the crack edges, blocking the crack tip by particles and dissipation of fracture energy by deflection of the cracks on larger particles. The degree of conversion increased after modification, mainly due to a decrease in the matrix resin viscosity. It was also shown that all dental materials were nontoxic according to ISO 10993-5, indicating that modified materials have great potential for commercialization and clinical applications.


2012 ◽  
Vol 23 (5) ◽  
pp. 508-514 ◽  
Author(s):  
Vinícius E. S. Gajewski ◽  
Carmem S. Pfeifer ◽  
Nívea R. G. Fróes-Salgado ◽  
Letícia C. C. Boaro ◽  
Roberto R. Braga

The organic phase of resin composites is constituted by dimethacrylate resins, the most common monomers being the bisphenol A diglycidildimethacrylate (BisGMA), its ethoxylated version (BisEMA), triethylene glycol dimethacrylate (TEGDMA) and urethane dimethacrylate (UDMA). This study compared the homopolymers formed from the monomers used in restorative dental composites in terms of their degree of conversion (DC) and reaction kinetics (by near infra-red spectroscopy, n=3), mechanical properties (flexural modulus and strength in three point-bending, FM and FS, respectively, n=15), water sorption and solubility (WS and SL, respectively - ISO 4049, n=5). Materials were made photopolymerizable by the addition of camphoroquinone/dimethylamine ethyl methacrylate. TEGDMA showed the highest DC, followed by BisEMA, UDMA and BisGMA, both at 10 min and at 24h (p<0.001). UDMA showed the highest rate of polymerization, followed by TEGDMA, BisEMA and BisGMA (H0=13.254, p<0.001). UDMA and TEGDMA presented similar FM, significantly higher (p<0.001) than BisEMA and BisGMA, which in turn present statistically similar values (p>0.001). For FS, UDMA presented the highest value (p<0.001), followed by TEGDMA, then by BisEMA and BisGMA, which were statistically similar (p>0.001). BisGMA showed the highest WS, and TEGDMA and BisEMA the lowest. UDMA was statistically similar to all (H0=16.074, p<0.001). TEGDMA presented the highest SL, followed by UDMA, BisGMA and BisEMA (p<0.001). The tested homopolymers presented different behaviors in terms of polymerization kinetics, flexural properties, water sorption and solubility. Therefore, the use of copolymers is justified in order to obtain high DC and mechanical properties, as well as good resistance to water degradation.


Author(s):  
Felicitas MAYINGER ◽  
Marcel REYMUS ◽  
Anja LIEBERMANN ◽  
Marc RICHTER ◽  
Patrick KUBRYK ◽  
...  

Author(s):  
Matthias Kelch ◽  
Bogna Stawarczyk ◽  
Felicitas Mayinger

Abstract Objective To investigate the degree of conversion (DC), Martens hardness (HM), elastic indentation modulus (EIT), and biaxial flexural strength (BFS) of six dual-polymerizing resin composite luting materials initially and after 2 and 7 days of aging. Materials and methods Specimens fabricated from Bifix QM (BIF; VOCO), Calibra Ceram (CAL; Dentsply Sirona), DuoCem (DUO; Coltène/Whaledent), G-CEM LinkForce (GCE; GC Europe), PANAVIA V5 (PAN; Kuraray Europe), and Variolink Esthetic DC (VAR; Ivoclar Vivadent) (n = 12 per material) were light-polymerized through 1 mm thick discs (Celtra Duo, Dentsply Sirona). DC, HM, and EIT were recorded directly after fabrication, and after 2 and 7 days of aging. As a final test, BFS was measured. Univariate ANOVAs, Kruskal–Wallis, Mann–Whitney U, Friedman, and Wilcoxon tests, and Weibull modulus were computed (p < 0.05). Results While CAL presented low DC, HM, EIT, and BFS values, DUO and BIF showed high results. Highest Weibull moduli were observed for VAR and DUO. DC and Martens parameters increased between the initial measurement and 2 days of aging, while aging for 7 days provided no further improvement. Conclusions The choice of dual-polymerizing resin composite luting material plays an important role regarding chemical and mechanical properties, especially with patients sensitive to toxicological issues. DUO may be recommended for bonding fixed dental prostheses, as it demonstrated significantly highest and reliable results regarding DC, HM, and BFS. As DC and HM showed an increase in the first 48 h, it may be assumed that the polymerization reaction is not completed directly after initial polymerization, which is of practical importance to dentists and patients. Clinical relevance The chemical and mechanical properties of dual-polymerizing resin composite luting materials influence the overall stability and long-term performance of the restoration.


Materials ◽  
2021 ◽  
Vol 14 (19) ◽  
pp. 5642
Author(s):  
Branislava Petronijevic Sarcev ◽  
Sebastian Balos ◽  
Dubravka Markovic ◽  
Ivan Sarcev ◽  
Marija Vukcevic ◽  
...  

The objective of this work was to measure and correlate the degree of conversion (DC), mechanical properties and monomer elution from self-, dual- and light-cured core composites. Five samples of each of the following materials were prepared for each test: Clearfil (Core, Photo Core, Automix), Bisco (Core-Flo, Light-Core and Bis-Core). DC was determined using FTIR, compressive and flexural strength and modulus of elasticity using a universal testing machine and microhardness using Vickers hardness. Elution was measured using HPLC. One-way ANOVA with Tukey’s post-test and Pearson’s correlation were used to statistically analyze the data. DC of Clearfil-Dual (70.1%) and Clerafil-Photo (66.8%) were higher than Clearfil-Self (55.4%) and all Bisco materials (51.4–55.3%). Flexural strength of Clearfilwas higher than that of Bisco composites. The Microhardness of Clearfil-Dual (119.8VHN) and Clearfil-Photo (118.0VHN) were higher compared to other materials. The greatest elution was detected from self-cured materials. DC positively correlated to microhardness and compressive/flexural strength and negatively to BisGMA elution. Clearfil-Photo and Automix showed higher conversion, lower monomer elution and, generally, better mechanical properties. Self-cured composites should not be recommended for routine clinical use as their performance was inferior to dual- and light-cured composites. Microhardness may be used as an indicator of elution.


Polymers ◽  
2021 ◽  
Vol 13 (24) ◽  
pp. 4415
Author(s):  
Codruta Sarosi ◽  
Marioara Moldovan ◽  
Andrada Soanca ◽  
Alexandra Roman ◽  
Timea Gherman ◽  
...  

(1) Background: This study investigated the influence of Bis-GMA, TEGDMA, UDMA, and two different polyethylene glycol (PEG)-containing, UDMO-based co-monomers on the Young’s modulus and flexural strength, degree of methacrylate C=C double bond conversion and residual monomer elution of experimental dental resins. (2) Methods: Urethane methacrylate-based monomer was synthesised via a radical chain growth polymerization mechanism using PEG in order to improve the mechanical properties. Dental resins were formulated using Bis-GMA, UDMA, or UDMO as base monomers combined with TEGDMA as a dilution monomer and DMAEM + CQ as the photo-initiator system. Degree of conversion (DC), mechanical properties, and residual monomer content of light-activated methacrylate resin formulations were evaluated and statistically analysed by ANOVA and a Tukey’s test. (3) Results: PEG-containing UDMO resins had lower Young’s modulus and elastic strength than UDMA-derived resin for all irradiation times. The highest DC (67,418%) was observed for the PEG-containing UDMO-based resin formulation when light cured for 40 s. For all samples, DC increased with the photo-polymerization time. The amount of residual monomer decreased after increasing the light-curing period from 20 to 40 s, resin with UDMO content 0.01 mol of PEG having the smallest amount of free eluted monomer. (4) Conclusions: A strong structure–property relationship exists in photo-cured dimethacrylate-based dental resins. The time and quantity of the photochemical initiation system can influence the physical–mechanical properties of the resins but also the monomers in their composition.


2020 ◽  
Vol 10 (5) ◽  
pp. 1628 ◽  
Author(s):  
Marta Piątek-Hnat ◽  
Kuba Bomba ◽  
Jakub Pęksiński

The aim of this work was synthesizing ester elastomers, using sorbitol as a monomer obtainable from renewable sources. Three polymers were synthesized, utilizing three different polycondensation times. Their mechanical and thermal properties were examined and compared. Poly(sorbitol sebacate-co-butylene sebacate) elastomers were synthesized as a result of polycondensation reaction, using sebacic acid, butylene glycol and sorbitol as monomers. Resulting materials had good mechanical properties and a cross-linked structure. Such elastomers are susceptible to hydrolytic degradation which has been confirmed in earlier studies. This paper shows that the material synthesized utilizing a 3.5 h polycondensation time has the most desirable mechanical and thermal properties, and the reaction is characterized by the highest degree of conversion of substrates.


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