WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

Permanent URI for this collectionhttps://hdl.handle.net/11147/7150

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  • Article
    Citation - WoS: 10
    Citation - Scopus: 10
    Determination of the Particle Interactions, Rheology and the Surface Roughness Relationship for Dental Restorative Ceramics
    (Elsevier Ltd., 2009) Kes, Mürşide; Polat, Hürriyet; Keleşoğlu, Serkan; Polat, Mehmet; Aksoy, Gökhan
    The effect of inter-particle interactions on the slurry properties and the final surface roughness of the dental ceramic restoratives was investigated. A commercial dental ceramic powder, IPS Empress 2 veneer, was used as the raw material. The magnitudes of the particle-particle interactions were computed by the DLVO theory for the ceramic slurries of different electrolyte solutions (0.1 M, 0.25 M, 0.5 M, 0.75 M, 1 M NaCl and CaCl2). As expected, the energies of particle-particle interactions were influenced significantly by the presence of electrolytes. These computations demonstrated that addition of electrolytes leads to a progressive depression of the repulsive double layer forces. The absence of these forces should inevitably lead to agglomeration caused by the ever-present van der Waals forces. The rheological measurements carried out using the slurries with same solution properties supported the findings of the DLVO computations. It was found that dental ceramic slurries showed a Newtonian behavior in the absence of electrolytes, which is indicative of little or no agglomeration in the slurry. On the other hand, the same slurries displayed a non-Newtonian, shear thinning behavior in the presence of electrolytes which can be attributed to agglomeration or gelation. Roughness of the ceramic surfaces produced from these slurries was studied by SEM analysis and profilometer measurements. Contact angle studies were also carried out on the same surfaces. It was observed that the surface became rougher initially with electrolyte addition to a maximum, most probably due to formation of isolated agglomerates due to a reduction of the repulsive double layer forces. After reaching a maximum, surface roughness decreased to a much lower value with further increase in electrolyte concentration. This was most probably caused by the formation of a relatively homogeneous, gel-like structure within the extensively agglomerated slurry due to a complete collapse of the double layer.
  • Article
    Citation - WoS: 12
    Citation - Scopus: 12
    Dispersion of Organophilic Ag Nanoparticles in Ps-Pmma Blends
    (Elsevier Ltd., 2015) Tüzüner, Şeyda; Demir, Mustafa Muammer.
    Abstract The preparation of stable composites with well-controlled particle location is one of the challenges in formulating new polymer/nanoparticle mixtures. In this study, cetyltriammonium bromide (CTAB)-capped monodisperse Ag nanoparticles were prepared and mixed with an equimass blend of polystyrene (PS) and poly(methyl methacrylate) (PMMA) in solution. The surface of the blend film without nanoparticles showed spherical pits with a size of 4.5 μm in diameter. The integration of CTAB-capped nanoparticles into the blend film developed surface bumps with a size of 0.4 μm in diameter. The organophilic Ag nanoparticles were distributed heterogeneously in the immiscible PS-PMMA blend. When the diameter of particle domains reached approximately 20 nm, particles were preferentially located at the interface of the PS and PMMA domains. Larger particle domains with a diameter of 90 nm were found to be in the PMMA-rich phase. Isothermal post-treatment of the PS-PMMA/Ag composite films directs the particle domains into PS domains. Thermodynamic factors that contribute to the observed morphologies are discussed.