Sürdürülebilir Yeşil Kampüs Koleksiyonu / Sustainable Green Campus Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7755
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Master Thesis A Chromatographicstudy of Carbon Monoxide Adsorption in Clinoptilolite(Izmir Institute of Technology, 2001) Narin, Güler; Ülkü, SemraAdsorption equilibrium and kinetic parameters for CO/clinoptilolite adsorbate/adsorbent pair were determined by perturbation gas chromatography. Chromatographic experiments were performed at temperatures in the 60-120°C range and at carrier gas flow rates in the range of 10.31-24.36 em/sec. The chromatographic response peaks were obtained by concentration pulse method. A packed column of 10 em length and 0.46 em inlet diameter which was packed with clinoptilolite particles with narrow size distribution (500-850 §) around mean diameter of301.9 § was used. The clinopti10lite particles were excavated from Gordes, Western Anatolia. The moments of the response peaks were calculated by integration of experimental chromatographic data and matched to the .model parameters in order to determine the equilibrium constants and diffusion coefficients. The dynamic model (Haynes and Sarma, 1973) was applied to describe the adsorption and diffusion processes in the packed column. This model includes axial dispersion, external mass transfer resistance, micropore and mesopore diffusion resistances. The equilibrium constants (Henry's law constants, K) were calculated in the range of 40 - 952 and were found to be in good agreement with the results in the literature. These constants were found to decrease with increasing temperature. The heats of adsorption were obtained in the range of 54.15 - 57.14 kl/mol from the slope of van't Hoff plots and compared with those in the literature. The heats of adsorption were found to be lower than those reported in the literature obtained for the same adsorbate/adsorbent pair. The higher heats of adsorption were explained by the smaller pore size, higher cation content of the clinoptilolite and more accessibility of the cations in the clinoptilolite framework by CO molecules. Heats of adsorption remained almost constant over the carrier gas velocity range studied. The contributions of axial dispersion and other mass transfer resistances Indiffusion of CO in clinoptilolite were also determined. The total dispersion exhibited slight change (average 0.035 see) with temperature implying that the micropore diffusional resistance was not dominant for diffusion of CO in clinoptilolite under the experimental conditions studied. The axial dispersion coefficient was determined in the range of 1.149.88 cm2/sec and the total mass transfer resistances were found between 0,02-0.06 sec. The results showed that the mesopore diffusion resistance was the controlling mechanism in CO diffusion in clinoptilolite. Mesopore diffusion coefficient was estimated as 2.98xlO-3 cm2/sec. This value was in good agreement with the theoretically determined value.Master Thesis Removal of Heavy Metals From Wastewaters by Use of Natural Zeolites(Izmir Institute of Technology, 2001) Türkmen, Müşerref; Ülkü, SemraIn the present study, clinoptilolite rich local natural zeolite was proposed as an ion-exchanger for the removal of heavy metals (Pb2+, Cu2+, Zn2+) from wastewaters.Natural zeolite samples were exposed to a simple pretreatment process which included washing and drying to remove impurities and dust.Thermal and adsorption related properties of washed and original zeolite samples were determined by TGA and N2 adsorption analyses. In TGA analyses, average water content for washed and original samples were found as 9.44 and 10.13 % respectively. In N2 adsorption studies, both washed and original samples showed the characteristic Type IIb isotherm. BET surface areas of the samples were calculated as 39.73 and 47.72 m2/g for washed and original samples respectively.Pretreatment process was found to improve the adsorption capacity of clinoptilolite due to the removal of impurities and dust.In ion-exchange studies, efficiency of natural zeolite in removal of heavy metals from the solutions was investigated based on some physical and chemical variables. For this purpose, particle size and the amount of zeolite in the solution, contact time of the metal containing solution with zeolite were selected as physical variables and pH, metal concentration of the solution, and the presence of other ions were selected as chemical variables. The chemical analyses of all exchange solutions were performed by using ICP-AES. Removal % of the metal ions from the solutions were obtained. Based on the experimental results, zeolite exhibited a significant affinity to Pb2+, followed by Cu2+ and Zn2+ even in the presence of competing cations.To test the applicability of natural zeolite for the treatment of Acid Mine Drainage (AMD), zeolite samples were allowed to contact with simulated AMD solutions.Consequently, natural zeolite was found to be an efficient ion exchanger for removing lead, copper and zinc ions from aqueous solutions.Master Thesis Investigation of Fuel Oxygenate Adsorption on Clinoptilolite Rich Natural Zeolite(Izmir Institute of Technology, 2006) Yetgin, Senem; İnal, FikretThe wide use of fuel oxygenates in gasoline as anti-knocking and emission reduction agent have recently led to serious environmental concerns due to their detection in groundwater and surface water. Among the various gasoline additives, methyl tertiary butyl ether (MTBE) and ethyl tertiary butyl ether (ETBE) are the most frequently used fuel oxygenates worldwide. Due to the physical and chemical properties of fuel oxygenates, the conventional treatment technologies are generally ineffective for their removal from contaminated water. Adsorption is a common process frequently used to remove fuel oxygenates from water. The use of natural zeolites as adsorbent have increased significantly because of their availability and low cost. Clinoptilolite is one of the most abundant zeolites in nature, and Turkey has very large clinoptilolite reserves. In this project the adsorption properties of clinoptilolite rich natural zeolites for use in the removal of MTBE and ETBE from water have been investigated using batch equilibrium and fixed-bed column experiments. The adsorption properties have been compared with those of two activated carbons (i.e., Powdered Activated Carbon (PAC) and Granulated Activated Carbon (GAC)). In addition, bisolute (i.e., benzene and oxygenate) adsorption experiments were also carried out to determine the effectiveness of these adsorbents in the presence of other gasoline hydrocarbons. All the experiments were performed at 25 °C with initial oxygenate and benzene concentrations of 2000 ppb and 400 ppb, respectively. In batch equilibrium experiments, it has been found that the powdered and granulated activated carbons had higher adsorption capacities for MTBE and ETBE than clinoptilolite. The highest capacity for the amount of MTBE adsorbed per unit mass of adsorbent was achieved using GAC while that of ETBE was obtained using PAC. The presence of benzene decreased the adsorption capacities of GAC and PAC. However, the effect of benzene was not clear and was dependent on the adsorbent loading for clinoptilolite. In fixed-bed column experiments, GAC and clinoptilolite were tested as adsorbents. The column breakthrough curves for clinoptilolite were steep indicating fast adsorption and narrow mass transfer region. For GAC, mass transfer regions were wider due to the relatively flat breakthrough curves. There was no significant effect of benzene on the breakthrough curves for GAC and clinoptilolite.Master Thesis Preconcentration and Atomic Spectrometric Determination of Rare Earth Elements (rees) in Environmental Samples(Izmir Institute of Technology, 2004) Pasinli, Türker; Eroğlu, Ahmet EminDetermination of rare earth elements (REEs) in environmental samples is usually performed by the plasma techniques, inductively coupled plasma optical emission spectrometry (ICP-OES) and inductively coupled plasma mass spectrometry (ICP-MS). Due to low concentrations of REEs and usually the presence of heavy matrix, an efficient separation and preconcentration technique is required prior to instrumental measurements in order to achieve accurate and reliable results. In this study, different types of zeolites (Clinoptilolite, Mordenite, Zeolite Y, Zeolite Beta), ion exchangers (Amberlite CG-120, Amberlite IR-120, Rexyn 101, Dowex 50W X18) and chelating resins (Muromac, Chelex 100, Amberlite IRC-718) were proposed as adsorbent materials for the preconcentration of REEs in environmental waters prior to their determination by ICP-OES. It was shown that REEs can be retained by these adsorbents quantitatively in a broad pH range (pH>4) and their desorptions from the adsorbents can be realized with acidic eluents. Of the sorbents investigated, clinoptilolite was chosen for the subsequent studies. Spike recovery tests were performed at various concentration levels in different water types including pure water, bottled drinking water, river water, sea water, and tap water, and were found to change between 85-90%.