Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection

Permanent URI for this collectionhttps://hdl.handle.net/11147/7148

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Subject: search.filters.subject.ZeolitesWoS Q: search.filters.wosQuartile.Q2

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Now showing 1 - 5 of 5
  • Article
    Citation - WoS: 5
    Citation - Scopus: 8
    Investigation of Structural Properties of Clinoptilolite Rich Zeolites in Simulated Digestion Conditions and Their Cytotoxicity Against Caco-2 Cells in Vitro
    (Springer Verlag, 2013) Kavak, Dilek Demirbüker; Ülkü, Semra
    The use of the clinoptilolite rich natural zeolites in biomedical applications such as in anticancer therapy, drug or drug support systems and as nutritive supplement is highly dependent on their behavior in digestive conditions. Aim of this study is to investigate structural stability of clinoptilolite rich natural zeolites in simulated digestion conditions and their interactions with digestive media and with Caco-2 (human colon adenocarcinoma) cells. X-ray Diffraction (XRD), Fourier Transform InfraRed (FTIR), Scanning Electron Microscopy (SEM) and Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES) analyses of the clinoptilolite rich zeolite samples showed that zeolites preserved their structural stabilities during in vitro digestion. Slight interactions were detected in UV measurements of the digestive liquid media and FTIR spectra of the intestinal digested media powders. SEM results implied that zeolites might have a role in the aggregation of the digestive enzymes. Cytotoxicity test using colon cancer cells showed that clinoptilolite rich natural zeolites have cytotoxic effect against Caco-2 cells and cytotoxicity did not significantly change with respect to simulated digestion process.
  • Article
    Citation - WoS: 10
    Citation - Scopus: 11
    Removal of Bacteria by Clinoptilolite Rich Mineral and Its Surfactant Modified Forms
    (Springer Verlag, 2013) Cansever Erdoğan, Beyhan; Ülkü, Semra
    Batch experiments were carried out to understand the potential values of clinoptilolite rich mineral and its surfactant modified forms in the removal of Gram-positive and Gram-negative bacteria. Zeta potential and Fourier Transform IR analysis were performed to explain the possible interactions between the bacteria and the zeolite samples. The results revealed that hydrogen bonding was significant mechanism in the removal of bacteria with clinoptilolite rich mineral and anionic surfactant modified clinoptilolite rich mineral whereas both attractive electrostatic forces and hydrogen bonding were dominant mechanism in the removal of bacteria with cationic surfactant modified clinoptilolite rich mineral. Cationic and anionic surfactant modified clinoptilolite rich mineral are promising materials in removal of bacteria studies.
  • Article
    Citation - WoS: 29
    Citation - Scopus: 31
    Cure Kinetics of Epoxy Resin-Natural Zeolite Composites
    (Springer Verlag, 2008) Cansever Erdoğan, Beyhan; Seyhan, Abdullah Tuğrul; Ocak, Yılmaz; Tanoğlu, Metin; Balköse, Devrim; Ülkü, Semra
    The cure kinetics of epoxy resin and epoxy resin containing 10 mass% of natural zeolite were investigated using differential scanning calorimetry (DSC). The conformity of the cure kinetic data of epoxy and epoxy-zeolite system was checked with the auto-catalytic cure rate model. The results indicated that the hydroxyl group on the zeolite surface played a significant role in the autocatalytic reaction mechanism. This group was able to form a new transition state between anhydride hardener and epoxide group. The natural zeolite particles acted as catalyst for the epoxy system by promoting its curing rate.
  • Article
    Citation - WoS: 11
    Citation - Scopus: 13
    Liquid-Phase Oxidation of Carvacrol Using Zeolite-Encapsulated Metal Complexes
    (American Chemical Society, 2006) Güneş, Alev; Bayraktar, Oğuz; Yılmaz, Selahattin
    We report here the use of zeolite-encapsulated metal (salpn) complexes as catalysts in the oxidation reaction of the natural compound carvacrol in acetonitrile with hydrogen peroxide as the oxidant. No previous studies on the oxidation of carvacrol in the presence of metal salpn complexes have been reported. By using a general flexible ligand method, Cr(III), Fe(III), Bi(III), Ni(II), and Zn(II) complexes of N,N′-bis(salicylidene)propane1,3-diamine (H2salpn) encapsulated in NaY zeolite were prepared. All catalysts were characterized by Fourier transform infrared (FTIR), X-ray diffraction (XRD), and scanning electron microscopy (SEM) analyses to confirm the complex encapsulation. The activities of all prepared catalysts for the oxidation of carvacrol and hydrogen peroxide were tested. The performances of all catalysts were compared on the basis of the leaching test results and carvacrol conversions. Thymohydroquinone and benzoquinones were observed as byproducts at high conversions of carvacrol. No product was formed in the absence of a catalyst. Fe(salpn)-NaY catalyst exhibited the highest carvacrol conversion of 27.6% with a yield of 22.0%, followed by Cr(salpn)-NaY catalyst with 23.5% carvacrol conversion and a yield of 17.6%. Other catalysts have shown relatively lower performances in terms of carvacrol conversion and leaching. The Cr(salpn)-NaY catalyst was found to be a more efficient catalyst than others on the basis of leaching and activity tests. With the selected catalyst Cr (salpn)-NaY, the effects of temperature and carvacrol/hydrogen peroxide molar ratio on carvacrol oxidation reactions were investigated. Increasing the temperature from 40 to 60 °C caused an increase in the thymoquinone yield from 6.2% to 16.0%. An increase in carvacrol/hydrogen peroxide molar ratio from 1 to 3 resulted in a decrease in the thymoquinone yield.
  • Article
    Citation - WoS: 15
    Citation - Scopus: 16
    Coke Content of Spent Commercial Fluid Catalytic Cracking (fcc) Catalysts: Determination by Temperature-Programmed Oxidation
    (Springer Verlag, 2003) Bayraktar, Oğuz; Kugler, Edwin L.
    Zeolite catalysts are widely used in oil refinery and petrochemical industries. Fluid catalytic cracking (FCC) catalysts used in a refinery consist of Y zeolite, a silica-alumina matrix and a binder. In this study, spent FCC catalysts were prepared by cracking sour imported heavy gas oil (SIHGO) in a microactivity test unit. The total amount of coke and the hydrogen-to-carbon ratio (H/C) in the coke for spent FCC catalysts contaminated with metals were determined using temperature-programmed oxidation (TPO). Total H/C ratios of the coke on FCC catalysts were found to be in the range of 0.4 to 1, indicating the majority of the coke consists of polyaromatic species. H/C ratio decreased with increasing coke contents on the catalysts. This ratio was found to be higher for the catalyst with high metal concentration compared to the catalyst with relatively low metal concentration. The high H/C ratio for highly contaminated FCC catalyst was attributed to the formation of hydrogen rich coke by hydrogenation reactions catalyzed by the contaminant metals on the catalyst. After hydrogen pre-treatment both coke amount and H/C ratio decreased significantly. This was due to the decrease in the hydrogenation activities of the contaminant-metals in their reduced forms.