Chemical Engineering / Kimya Mühendisliği

Permanent URI for this collectionhttps://hdl.handle.net/11147/14

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  • Article
    Citation - WoS: 3
    Citation - Scopus: 2
    Adsorption of No in Clinoptilolite-Rich Zeolitic Mineral by Concentration Pulse Chromatography Method
    (Elsevier Ltd., 2016) Narin, Güler; Ülkü, Semra
    The equilibrium and kinetic parameters for NO adsorption in a clinoptilolite-rich natural zeolitic material from Turkey were determined using the concentration pulse chromatography method. Under the experimental conditions (carrier gas velocities and adsorption temperatures) the micropore diffusion resistance was found to be the mass transfer controlling step. Matching the first moment of the response peaks to the mathematical model the Henry's Law constants and heat of adsorption at zero loading were determined. The axial dispersion, external film, macropore and micropore diffusion coefficients, and activation energy for diffusion of NO in the micropores were calculated from the analysis of the second moments of the response peaks. For successive NO pulses without regeneration between the pulses, the retention times of the response peaks decreased and peak areas increased with the injection number indicating irreversible adsorption. The reversibly adsorbed NO could be desorbed by purging with an inert gas at the adsorption pressure and temperature. Temperature programmed desorption profile obtained by heating the NO saturated adsorbent to 400 °C under inert flow revealed presence of multiple irreversibly adsorbed species in NZ with different thermal stabilities. Desorption of these species was not achieved during the heating up to 400 °C which makes the natural zeolitic materıal suitable for NO storage rather than for cyclic adsorptive separation processes.
  • Article
    Citation - WoS: 12
    Citation - Scopus: 17
    Diffusion Mechanism of Water Vapour in a Zeolitic Tuff Rich in Clinoptilolite
    (Springer Verlag, 2008) Çakıcıoğlu Özkan, Seher Fehime; Ülkü, Semra
    The adsorption kinetics of H2O in a clinoptilolite rich zeolitic tuff was experimentally investigated at 18°C. In the identification of the diffusion mechanism the isothermal adsorption model equation was used. It was found out that the intraparticle mass transfer becomes more dominant over the heat transfer with increase in particle size and the adsorptive dose pressure. Although initially intraparticle mass transfer was the controlling resistance later external heat transfer also contributes to the transfer mechanism.
  • Article
    Citation - WoS: 4
    Citation - Scopus: 4
    A Chromatographic Study of Carbon Monoxide Adsorption on a Clinoptilolite-Containing Natural Zeolitic Material
    (Taylor and Francis Ltd., 2004) Narin, Güler; Yılmaz, Selahattin; Ülkü, Semra
    In this study, the equilibrium and kinetic parameters for CO adsorption on clinoptilolite-rich natural zeolitic material were determined by the concentration pulse chromatography technique. Experiments were carried out at different column temperatures (60-120°C) and interstitial carrier gas velocities (3.1-16.3 cm/s) using a clinoptilolite-rich natural zeolitic material packed column. The equilibrium and kinetic parameters were determined by matching the moments of the experimentally obtained response curves to the parameters in the mathematical model. The Henry's Law constants were found to decrease from 700 to 49 with increasing temperature. The heat of adsorption at low coverage was found to be 50.73 kJ/molK. The contributions from external film, macropore, and micropore diffusion resistances to mass transfer were determined, and the micropore diffusion resistance was found to be the major contributor. The micropore diffusivity as a function of crystal radius (Dc/rc 2) was determined and found to change between 5.72 × 10-4 and 1.34 × 10-2 s-1 in the temperature range studied.
  • Article
    Citation - WoS: 13
    Citation - Scopus: 15
    A Study of Adsorption of Water Vapour on Wool Under Static and Dynamic Conditions
    (Springer Verlag, 1998) Ülkü, Semra; Balköse, Devrim; Çağa, Tayfun; Özkan, Fehime; Ulutan, Sevgi
    Adsorption of water vapour on wool provides not only textile comfort, but also convenience in transportation due to increase in its bulk density. The adsorption and desorption isotherms of water vapour for wool were determined by both volumetric technique using a Coulter Omnisorp 100CX instrument and gravimetric method employing a Cahn 2000 electronic microbalance. Adsorption isotherm fitting to B.E.T. model and hysteresis on desorption was observed. The average effective diffusion coefficient of water in wool was found to be 8.4 × 10-14 m2 s-1 at 25°C from gravimetric data. The effects of packing height and air velocity on the breakthrough curves were also investigated in the wool packed columns. For pseudo first order model, k values changing between 0.33 × 10-6 -69 × 10-6 s-1 was obtained for 2.2-6.4 cm s-1 air velocity and 0.05-0.20 m packing height ranges.