The performance and service life of glass-or ceramic-filled polymeric composites depend on the nature of their resin, filler and interfacial phases as well as the efficacy of the polymerization process. The synergy that exists between the organic polymer matrix and the usually inorganic reinforcing filler phase is principally mediated by the interfacial/interphasial phase. This latter phase develops as a result of the dual reactivity of a silane coupling agent, (YRSiX3), a bifunctional molecule capable of reacting with the silanol groups of glass or ceramic fillers via its silane functional group (–SiX3) to form Si-O-Si- bonds to filler surfaces, and also with the resin phase by graft copolymerization via its Y functional group, usually a methacrylic vinyl group. In this paper, we explore some of the chemistry of organosilanes, especially that of functional organosilanes (or silane coupling agents as they are commonly known) that are used to mediate interfacial bonding in mineral reinforced polymeric composites. The chemistry of organosilanes can be quite complex involving hydrolytically initiated self-condensation reactions in solvents (including monomers) that can culminate in polymeric silsesquioxane structures, exchange reactions with hydroxylated or carboxylated monomers to form silyl ethers and esters, as well as the formation of silane derived interfaces by adhesive coupling with siliceous mineral surfaces.
The mechanical properties of recently developed bioactive, antidemineralizing/remineralizing, amorphous calcium phosphate (ACP)-based composites need improvement. The objective of this study was to elucidate the effect of structure and composition of resins on the biaxial flexure strength (BFS) and the degree of conversion (DC) of composites attained after photo-polymerization. Two series of 2,2-bis[p-(2'-hydroxy-3'-methacryloxypropoxy)phenyl]propane (Bis-GMA)/triethylene glycol dimethacrylate (TEGDMA)/X (X being a neutral or acidic comonomer) ternary resins were prepared and mixed with a mass fraction of 40% of zirconia-hybridized ACP. Both unfilled copolymers and their composites were evaluated for BFS (dry and wet specimens after 2 weeks of immersion in buffered saline) and for DC (after 24 h at 23 degrees C). It was found that for the neutral X monomers, no correlation existed between the hydrophobic/hydrophilic character of the X monomer and the BFS values of the immersed composites. A flexible monomethacrylate yielded copolymers and composites with the highest DC. For the resins utilizing the acidic comonomers, methacrylic acid and mono-4-(methacryloyloxy) ethyltrimellitate (4MET), dry composites with improved BFS values were obtained. 4MET composites exhibited the least loss of strength of all the ternary resin ACP materials. The effect of acidic X on DC was most pronounced for maleic acid copolymers.
Precise measurements of fiber break regions have been made during the single fiber fragmentation test (SFFT) procedure on E‐glass/diglycidyl ether of bisphenol‐A (DGEBA)/meta‐phenylenediamine (m‐PDA) test specimens. From these measurements, the location and size of each fiber fragment was determined, and the resulting information was used to construct fragmentation maps of the tested fiber. By comparing these maps, the fragmentation process supports random fragmentation along the length of the fiber. Since the interfacial shear strength (IFSS) or the interfacial shear stress transfer coefficient (I‐STC) is obtained from the fragment length data at the end of the test (saturation), frequency histograms of the fragment length data were constructed to determine the repeatability of the fragmentation process. Since the SFFT is performed by sequential step‐strains of the test specimen, test protocols were developed by controlling the step size of each strain increment and the time between each step‐strain (dwell time). For the testing protocols used in this research, the E‐glass/DGEBA/m‐PDA frequency histograms of the fragment lengths were found to be generally repeatable. However, when the effective strain rate of the test was altered by changing the dwell time between strain increments, the fragment distribution at saturation of the E‐glass/DGEBA/m‐PDA SFFT specimens changed. The direction of the change was found to be inconsistent with the effect one might expect when only the nonlinear viscoelastic behavior of the matrix is considered. However, the magnitude of the change observed in the E‐glass/DGEBA/m‐PDA SFFT specimens is not universal. Fragmentation data obtained on E‐glass/polyisocyanurate SFFT specimens revealed a much smaller change in fragment length distributions with the same change in testing protocols. Consistent with the results obtained on the E‐glass/DGEBA/m‐PDA, fiber fragmentation occurs when the polyisocyanurate matrix exhibits nonlinear viscoelastic behavior. The implication of these results for interfacial shear strength measurements is discussed.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.