Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection

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

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Now showing 1 - 6 of 6
  • Article
    Citation - WoS: 13
    Citation - Scopus: 13
    Application of Work Function Measurements in the Study of Surface Catalyzed Reactions on Rh(1 0 0)
    (Taylor & Francis, 2018) Çağlar, Başar; Kızılkaya, Ali Can; Niemantsverdriet, J. W. (Hans); Weststrated, C. J. (Kees-Jan)
    The present article aims to show how work function measurements (WF) can be applied in the study of elementary surface reaction steps on metallic single crystal surfaces. The work function itself can in many cases not be interpreted directly, as it lacks direct information on structural and chemical nature of the surface and adsorbates, but it can be a powerful tool when used together with other surface science techniques which provide information on the chemical nature of the adsorbed species. We here, illustrate the usefulness of work function measurements using Rh(100) as our model catalyst. The examples presented include work function measurements during adsorption, surface reaction, and desorption of a variety of molecules relevant for heterogeneous catalysis. Surface coverage of adsorbates, isosteric heat of adsorption, and kinetic parameters for desorption, desorption/decomposition temperatures of surface species, different reaction regimes were determined by WF with the aid of other surface science techniques.
  • Article
    Citation - WoS: 6
    Citation - Scopus: 6
    Esterification of 1-Octanol on Clinoptilolite-Supported Tio2 Catalysts
    (Springer Verlag, 2019) Özyağcı, Bensu; Şahin, Volkan; Karabakan, Abdulkerim
    In this study, a natural type of zeolite, Clinoptilolite (CLI), is used as a support for TiO2. First, TiO2-supported heterogeneous catalysts originated from the high temperature calcination of TiCl4 groups, which were thermally immobilized on clinoptilolite, were obtained. Powder-XRD and EDX analyzes showed that the oxide form of Ti-immobilized on dealuminated clinoptilolite were formed in the anatase phase, and the zeolite structure was preserved. As seen in TGA/DTA analyzes, this catalyst could be efficient and have high stability for many reactions. Second, the esterification reaction of 1-octanol with acetic acid is used as a reference reaction for this catalyst.
  • Article
    Citation - WoS: 273
    Citation - Scopus: 327
    Transesterification of Nannochloropsis Oculata Microalga's Lipid To Biodiesel on Al2o3 Supported Cao and Mgo Catalysts
    (Elsevier Ltd., 2009) Umdu, Emin Selahattin; Tuncer, Mert; Şeker, Erol
    In this study, we present the activities of Al2O3 supported CaO and MgO catalysts in the transesterification of lipid of yellow green microalgae, Nannochloropsis oculata, as a function of methanol amount and the CaO and MgO loadings at 50 °C. We found that pure CaO and MgO were not active and CaO/Al2O3 catalyst among all the mixed oxide catalysts showed the highest activity. Not only the basic site density but also the basic strength is important to achieve the high biodiesel yield. Biodiesel yield over 80 wt.% CaO/Al2O3 catalyst increased to 97.5% from 23% when methanol/lipid molar ratio was 30.
  • Article
    Citation - WoS: 19
    Citation - Scopus: 23
    Influence of Microstructure on the Rheological Behavior of Dense Particle Gels
    (John Wiley and Sons Inc., 2005) Wyss, Hans M.; Deliormanlı, Aylin M.; Tervoort, Elena V.; Gauckler, Ludwig Julius
    Rheological measurements are performed on highly concentrated alumina gels. By using an in situ mechanism based on enzyme-catalyzed internal reactions, we are able to form gels of highly concentrated particles without disturbing the microstructures that develop during the gelation process. These gels are produced by two different destabilization mechanisms: Either the pH of the suspension is shifted toward the isoelectric point (ΔpH method) or the ionic strength of the suspension is increased at a constant pH (ΔI method). The two destabilization mechanisms lead to gels of significantly different microstructures. We find notable differences in the rheological behavior of the two systems, suggesting a bond-bending mechanism for stress transmission in the case of ΔpH gels and a bond-stretching mechanism in the case of ΔI gels. In addition, for both kinds of gels we compare the in situ properties to those obtained after altering the microstructure by shearing. Results suggest an increase in elastic and yield properties of concentrated particle gels with decreasing homogeneity of their microstructures.
  • Article
    Citation - WoS: 22
    Citation - Scopus: 23
    Acidic Sites in Beta Zeolites in Dependence of the Preparation Methods
    (Elsevier Ltd., 2004) Dimitrova, R.; Gündüz, Gönül; Dimitrov, L.; Tsoncheva, T.; Yılmaz, Selahattin; Urquieta-González, Ernesto Antonio
    Beta zeolites synthesized by different methods are compared in their structure peculiarities and acidic properties by nitrogen physisorption, IR-KBr, pyridine sorption-desorption and thermoprogrammed desorption of ammonia. It is found that mesopores could be obtained in beta zeolites with the change of the activation procedure. Methanol conversion to dimethyl ether and hydrocarbons is used as a test reaction for understanding of the acid center function.
  • Conference Object
    Citation - WoS: 7
    Citation - Scopus: 8
    Acylation of 2-Methoxynaphthalene Over Ion-Exchanged Ss-Zeolite
    (Elsevier Ltd., 2002) Kantarlı, İsmail Cem; Artok, Levent; Bulut, Hatice; Yılmaz, Selahattin; Ülkü, Semra
    Friedel-Crafts acylation of 2-Methoxynaphthalene was carried out over various ion-exchanged β zeolites (Mn+β, where Mn+: In3+, Zn2+, Al3+, Fe3+, La3+) with various anhydride (acetic, propionic and benzoic anhydrides), or acyl chloride (acetyl, propionyl and benzoyl chlorides) acylating reagents. The results suggested that selectivity towards the 6-substituted products was higher with the larger size anhydrides, propionic and benzoic anhydrides. The metal cation type within the zeolite significantly influenced the extent of conversion and product distribution. That La3+ exchanged zeolite displayed higher selectivity for the 6-position acylated product with anhydrides ascribed mainly to narrowing of channels by the presence of La(OH)2+ ions that leave no room for the formation of more bulky isomeric forms and to enhanced Bronsted acidity of the zeolite. With acyl chlorides, the recovery of ketone products was found to be remarkably low. 1-Acyl-2-methoxynaphthalenes actively underwent deacylation when acyl chlorides were used as the acylation reagent.