Researcher: Kartal, Ayşe Meriç
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Kartal, Ayşe Meriç
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Publication Metadata only Surface modification of silica aerogels by hexamethyldisilazane-carbon dioxide mixtures and their phase behavior(Elsevier Science Bv, 2010) N/A; N/A; Department of Chemical and Biological Engineering; Kartal, Ayşe Meriç; Erkey, Can; Master Student; Faculty Member; Department of Chemical and Biological Engineering; Graduate School of Sciences and Engineering; College of Engineering; N/A; 29633the surfaces of monolithic silica aerogels were rendered hydrophobic using hexamethyldisilazane (HMDS) as surface modification agent and scCO(2) as solvent. the treatment led to hydrophobic silica aerogels which are as transparent as untreated aerogels. the effects of HMDS concentration in the fluid phase and the reaction time were investigated and the contact angles were found to be 130 at different conditions. FTIR spectra indicated a reduction in hydrophilic surface silanol groups and the emergence of hydrophobic CH3 groups. the bubble point pressures of the HMDS-CO2 system were obtained at temperatures 298.2K, 313.2K, 327.7 K and 342 K at various concentrations. at a fixed temperature, the bubble point pressure decreased as the concentration of HMDS increased. at a fixed composition, bubble point pressure increased as the temperature increased. the bubble point pressures were modeled using the Peng-Robinson Stryjek-vera Equation of State (PRSveOS) and compared well with the experimental data.Publication Metadata only Controlled drug delivery through a novel PEG hydrogel encapsulated silica aerogel system(Wiley, 2012) N/A; N/A; N/A; Department of Chemical and Biological Engineering; Department of Chemical and Biological Engineering; Giray, Seda; Bal, Tuğba; Kartal, Ayşe Meriç; Kızılel, Seda; Erkey, Can; Master Student; PhD Student; Master Student; Faculty Member; Faculty Member; Department of Chemical and Biological Engineering; N/A; N/A; N/A; College of Engineering; College of Engineering; N/A; 353534; N/A; 28376; 29633A novel composite material consisting of a silica aerogel core coated by a poly(ethylene) glycol (PEG) hydrogel was developed. The potential of this novel composite as a drug delivery system was tested with ketoprofen as a model drug due to its solubility in supercritical carbon dioxide. The results indicated that both drug loading capacity and drug release profiles could be tuned by changing hydrophobicity of aerogels, and that drug loading capacity increased with decreased hydrophobicity, while slower release rates were achieved with increased hydrophobicity. Furthermore, higher concentration of PEG diacrylate in the prepolymer solution of the hydrogel coating delayed the release of the drug which can be attributed to the lower permeability at higher PEG diacrylate concentrations. The novel composite developed in this study can be easily implemented to achieve the controlled delivery of various drugs and/or proteins for specific applications. (C) 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A:, 2012.