Abstract Camphorquinone is the most conventionally used photoinitiator in Dentistry. Although different alternative photoinitiators have been proposed, no photoinitiator was capable of completely substituting camphorquinone. The combination of photoinitiators has been considered the best alternative. Objectives: To evaluate the effect of combining Norrish type I and II photoinitiators on the cure efficiency of dental resin-based composites. Methodology: Experimental composites were produced containing different photoinitiator systems: Norrish type I-only, mono-alkyl phosphine oxide (TPO); Norrish type II-only, camphorquinone (CQ); or its combination, CQ and TPO, in a 1: 1 molar ratio. UV-vis absorption spectrophotometry was performed to assess the consumption of each photoinitiator after curing (n=3). A multi-wave LED (Bluephase® G2, Ivoclar Vivadent) was pre-characterized and used with a radiant exposure of 24 J/cm2. The degree of conversion was evaluated by Raman spectrometry, and the elution of the monomers by nuclear magnetic resonance analysis (n=3). Data were analyzed using ANOVA and Tukey's test (α=0.05; β=0.2). Results: The combination of CQ and TPO increased the consumption of the photoinitiator system compared to CQ-only (p=0.001), but presented similar consumption compared to TPO-only (p=0.52). There was no significant difference in the degree of conversion between the composites regardless of the photoinitiator system (p=0.81). However, the elution of the monomers was reduced when both photoinitiators were combined. TPO-based material presented the highest elution of monomers. Conclusions: The combination of the photoinitiator systems seems to be beneficial for the cure efficiency of dental resin-based composites.

Abstract Carbon nanostructures have been extensively studied due to combination of properties they present. With different geometries and reactivities, carbon nanotubes, graphene and fullerene were oxidized and modified with octadecylamine (ODA) in order to decrease van der Waals’s interaction and consequently improve the polymer-carbon nanostructures affinity for use in nanocomposites. Nanostructures were characterized as morphology, chemical structure, molecular conformation and thermal properties. All nanostructures showed results that confirm the modification with ODA, without geometry being altered. Modified nanostructures showed different percentages of ODA: graphene 86%, carbon nanotubes 83% and fullerene 63%. It was attributed to distinct reactivities, shapes and specific surface area available, due to different amounts of reactive terminals obtained before oxidation reactions. However, they showed a lower interfacial interaction, which is highly favorable for use in polymer nanocomposites.