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Resin Matrix (resin + matrix)
Selected AbstractsEffect of particle size of an amorphous calcium phosphate filler on the mechanical strength and ion release of polymeric composites,JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2007Soo-Young Lee Abstract The random clustering of amorphous calcium phosphate (ACP) particles within resin matrices is thought to diminish the strength of their polymerized composites. The objective of this study was to elucidate the effect of ball-milling on the particle size distribution (PSD) of ACP fillers and assess if improved dispersion of milled ACP in methacrylate resin sufficiently enhanced filler/matrix interactions to result in improved biaxial flexure strength (BFS), without compromising the remineralizing potential of the composites. Unmilled and wet-milled zirconia-hybridized ACP (Zr-ACP) fillers were characterized by PSD analysis, X-ray diffraction, thermogravimetric and chemical analysis, infrared spectroscopy, and scanning electron microscopy. Composite specimens made from a photoactivated, ternary methacrylate resin admixed with a mass fraction of 40% of un-milled or milled Zr-ACP were evaluated for the BFS (dry and wet) and for the release of calcium and phosphate ions into saline solutions. While having no apparent effect on the structure, composition, and morphology/topology of the fillers, milling significantly reduced the average size of Zr-ACP particulates (median diameter, dm = 0.9 ± 0.2 ,m) and the spread of their PSD. Better dispersion of milled Zr-ACP in the resins resulted in the improved BFS of the composites, even after aqueous soaking, and also gave a satisfactory ion release profile. The demonstrated improvement in the mechanical stability of anti-demineralizing/remineralizing ACP composites based on milled Zr-ACP filler may be beneficial in potentially extending their dental utility. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2007 [source] Effect of chemical modifications on the thermal stability and degradation of banana fiber and banana fiber-reinforced phenol formaldehyde compositesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2008Seena Joseph Abstract Banana fiber has been modified by treatments with sodium hydroxide, silanes, cyanoethylation, heat treatment, and latex treatment and the thermal degradation behavior of the fiber was analyzed by thermogravimetry and derivative thermogravimetry analysis. Both treated and untreated fibers showed two-stage decomposition. All the treatments were found to increase the thermal stability of the fiber due to the physical and chemical changes induced by the treatments. The thermal degradation of treated and untreated banana fiber-reinforced phenol formaldehyde composites has also been analyzed. It was found that the thermal stability of the composites was much higher than that of fibers but they are less stable compared to neat PF resin matrix. Composite samples were found to have four-stage degradation. The NaOH treated fiber-reinforced composites have very good fiber/matrix adhesion and hence improvement in thermal stability is observed. Though both silane treatments increased the thermal stability of the composite the vinyl silane is found to be more effective. Heat treatment improves the crystallinity of the fiber and decreases the moisture content, hence an improved thermal stability. The latex treatment and cyanoethylation make the fiber surface hydrophobic, here also the composite is thermally more stable than untreated one. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci 2008 [source] Tribological properties of bismaleimide composites with surface-modified SiO2 nanoparticlesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2008Hongxia Yan Abstract In this article, the surface of SiO2 nanoparticles was modified by silane coupling agent N -(2-aminoethyl)-,-aminopropylmethyl dimethoxy silane. The bismaleimide nanocomposites with surface-modified SiO2 nanoparticles or unmodified SiO2 nanoparticles were prepared by the same casting method. The tribological performance of the nanocomposites was studied on an M-200 friction and wear tester. The results indicated that the addition of SiO2 nanoparticles could decrease the frictional coefficient and the wear rate of the composites. The nanocomposites with surface-modified SiO2 nanoparticles showed better wear resistance and lower frictional coefficient than that with the unmodified nanoparticles SiO2. The specific wear rate and the steady frictional coefficient of the composite with 1.0 wt % surface-modified SiO2 nanoparticles are only 1.8 × 10,6 mm3/N m and 0.21, respectively. The dispersion of surface-modified SiO2 nanoparticles in resin matrix was observed with transmission electron microscope, and the worn surfaces of pure resin matrix and the nanocomposites were observed with scanning electron microscope. The different tribological behavior of the resin matrix and the filled composites should be dependent on their different mechanical properties and wear mechanism. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Effect of monomer composition on crystal growth by resin containing bioglassJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2010Masanori Hashimoto Abstract This study evaluated the effect of resin monomer composition on crystal growth at the interface between the resin/bioglass composites and water. Light-cured resin that contained 2-bis[4(2-hydroxy-3-methacryloyloxy-propyloxy)-phenyl], 2-hydroxyethyl methacrylate, and triethylene glycol dimethacrylate with different compositions were used. Resin/bioglass composites were prepared with 40 mass% bioglass and 60 mass% resin. The resin/bioglass composites were stored in deionized distilled water for 24 h (control group) or 3,12 months (experimental groups). After water storage, the disk surfaces were examined by light- and scanning electron microscopy. Chemical states of the crystals were analyzed by laser-Raman spectroscopy and micro-X-ray diffractometry. The microscopic analysis showed crystal on the resin disks surface after six months of water storage for hydrophilic resins. However, there was no crystal formation in the control and the experimental groups of specimens of hydrophobic resins. Raman analysis showed the chemical states of the crystals formed on the resin matrix and bioglass to be different. The micro-X-ray analysis of crystals on resin disks identified them to be calcium carbonate. This crystal formation occurred in water instead of simulated body fluid. In conclusion, the resin monomer compositions affected the ability to induce crystal growth on the surfaces of disks containing bioglass. © 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2010 [source] Chlorhexidine release and antibacterial properties of chlorhexidine-incorporated polymethyl methacrylate-based resin cementJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2010N. Hiraishi Abstract This study evaluated chlorhexidine release from experimental, chlorhexidine-incorporated polymethyl methacrylate (PMMA)-based resin cements prepared from Super-Bond C&B (Sun Medical) and examined the antimicrobial activity against Streptococcus mutans and Enterococcus faecalis. Chlorhexidine diacetate was added into PMMA polymer to obtain chlorhexidine concentration of 0.0, 1.0, 2.0, 3.0, and 4.0 wt %. Chlorhexidine-incorporated, cured resin disks were immersed in distilled water at 37°C for 5 weeks, and the chlorhexidine release was analyzed by high-performance liquid chromatography. The antibacterial effect of freshly mixed resin cements was examined using the agar diffusion test. For the direct contact test, the wells (n = 6) of microtiter plates were coated with cements. The coated wells were aged up to 3 weeks prior to the placement of bacterial suspensions directly on cured cements. The 3.0 and 4.0% chlorhexidine-incorporated cement exhibited chlorhexidine release for 5 weeks; however, more than 98% of chlorhexidine was retained in resin matrix. No release was detected from the 1.0 and 2.0% incorporated cement at 1 week and 2 weeks, respectively. The agar diffusion test failed to detect antibacterial effects against Enterococcus faecalis, whereas the direct contact test revealed the antibacterial effect of 3.0 and 4.0% incorporated cements against each microbe for 2 weeks. The 3.0 and 4.0% chlorhexidine-incorporated resin cement possessed prolonged chlorhexidine release and antibacterial properties for 2 weeks. © 2010 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2010 [source] Sorption kinetics of ethanol/water solution by dimethacrylate-based dental resins and resin compositesJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2007Irini D. Sideridou Abstract In the present investigation the sorption,desorption kinetics of 75 vol % ethanol/water solution by dimethacrylate-based dental resins and resin composites was studied in detail. The resins examined were made by light-curing of bisphenol A glycol dimethacrylate (Bis-GMA), triethylene glycol dimethacrylate (TEGDMA), urethane dimethacrylate (UDMA), bisphenol A ethoxylated dimethacrylate (Bis-EMA), and mixtures of these monomers. The resin composites were prepared from two commercial light-cured restorative materials (Z100 MP and Filtek Z250), the resin matrix of which is based on copolymers of the above-mentioned monomers. Ethanol/water sorption/desorption was examined in both equilibrium and dynamic conditions in two adjacent sorption,desorption cycles. For all the materials studied, it was found that the amount of ethanol/water sorbed or desorbed was always larger than the corresponding one reported in literature in case of water immersion. It was also observed that the chemical structure of the monomers used for the preparation of the resins directly affects the amount of solvent sorbed or desorbed, as well as sorption kinetics, while desorption rate was nearly unaffected. In the case of composites studied, it seems that the sorption/desorption process is not influenced much by the presence of filler. Furthermore, diffusion coefficients calculated for the resins were larger than those of the composites and were always higher during desorption than during sorption. Finally, an interesting finding concerning the rate of ethanol/water sorption was that all resins and composites followed Fickian diffusion kinetics during almost the whole sorption curve; however, during desorption the experimental data were overestimated by the theoretical model. Instead, it was found that a dual diffusion,relaxation model was able to accurately predict experimental data during the whole desorption curve. Kinetic relaxation parameters, together with diffusion coefficients, are reported for all resins and composites. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2006 [source] Nonaqueous synthesis of nanosilica in epoxy resin matrix and thermal properties of their cured nanocompositesJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 2 2006Tzong-Ming Lee Abstract Nonaqueous synthesis of nanosilica in diglycidyl ether of bisphenol-A epoxy (DGEBA) resin has been successfully achieved in this study by reacting tetraethoxysilane (TEOS) directly with DGEBA epoxy matrix, at 80 °C for 4 h under the catalysis of boron trifluoride monoethylamine (BF3MEA). BF3MEA was proved to be an effective catalyst for the formation of nanosilica in DGEBA epoxy under thermal heating process. FTIR and 29Si NMR spectra have been used to characterize the structures of nanosilica obtained from this direct thermal synthetic process. The morphology of the nanosilica synthesized in epoxy matrix has also been analyzed by TEM and SEM studies. The effects of both the concentration of BF3MEA catalyst and amount of TEOS on the diameters of nanosilica in the DGEBA epoxy resin have been discussed in this study. From the DSC analysis, it was found that the nanosilica containing epoxy exhibited the same curing profile as pure epoxy resin, during the curing reaction with 4,4,-diaminodiphenysulfone (DDS). The thermal-cured epoxy,nanosilica composites from 40% of TEOS exhibited high glass transition temperature of 221 °C, which was almost 50 °C higher than that of pure DGEBA,DDS,BF3MEA-cured resin network. Almost 60 °C increase in thermal degradation temperature has been observed during the TGA of the DDS-cured epoxy,nanosilica composites containing 40% of TEOS. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 757,768, 2006 [source] Effect of grafting alkoxysilane on the surface properties of Kevlar fiberPOLYMER COMPOSITES, Issue 3 2007Tao Ai This research applied the methodology of metalation and grafting alkoxysilane to modify the surface of Kevlar-29 fiber. The surface properties of the modified Kevlar fiber were characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, atomic force microscopy, and Brunauer-Emmett-Teller isothermal adsorption analysis. The relationship between surface characteristics of Kevlar fiber and its interfacial adhesion of Kevlar fiber-reinforced epoxy resin composites was also discussed. Compared with the untreated fiber, the surface of the modified Kevlar fiber was much rougher, its oxygen content increased by about 12%, the surface area enlarged about 10 times, and the wetting behavior improved. Due to the modification of the fiber, the adhesion between the fiber and the resin matrix was markedly improved and the Interlaminar Shear Strength of its epoxy composites increased by about 57%. POLYM. COMPOS. 28:412,416, 2007. © 2007 Society of Plastics Engineers. [source] Compaction of fiber reinforcementsPOLYMER COMPOSITES, Issue 3 2002Gibson L. Batch In resin transfer molding, dry fiber reinforcements are compacted as the mold closes before injection of a curable resin matrix. This paper presents experimental data of compaction pressure as a function of fiber volume fraction. Data are presented for woven roving mats, random fiber mats, loose fiber rovings for pultrusion, and uniaxial or biaxial roving mats. These data are fit to a mathematical model derived in an Appendix. Experimental data are also given for six combinations of reinforcements. We use the compaction model of each constituent layer to predict the average volume fraction assuming that fiber layers do not interact. However, we see that most combinations of reinforcements have fiber volume fractions greater than expected at pressures under 50 psi, indicating a synergistic packing between the layers of different composition. [source] | ||||||||||