Browsing by Author "Soylu, A. M."

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    Influence of the sol – gel preparation method on the photocatalytic NO oxidation performance of TiO2/Al2O3 binary oxides
    (Elsevier, 2015-03-01) Soylu, A. M.; Polat, M.; Erdogan, D. A.; Erguven, H.; Ozensoy, E.; Vovk, E. I.
    In the current work, TiO2/Al2O3 binary oxide photocatalysts were synthesized via two different sol-gel protocols (P1 and P2), where various TiO2 to Al2O3 mole ratios (0.5 and 1.0) and calcination temperatures (150-1000 degrees C) were utilized in the synthesis. Structural characterization of the synthesized binary oxide photocatalysts was also performed via BET surface area analysis, X-ray diffraction (XRD) and Raman spectroscopy. The photocatalytic NO(g) oxidation performances of these binary oxides were measured under UVA irradiation in a comparative fashion to that of a Degussa P25 industrial benchmark. TiO2/Al2O3 binary oxide photocatalysts demonstrate a novel approach which is essentially a fusion of NSR (NOx storage reduction) and PCO (photocatalytic oxidation) technologies. In this approach, rather than attempting to perform complete NOx reduction, NO(g) is oxidized on a photocatalyst surface and stored in the solidstate. Current results suggest that alumina domains can be utilized as active NOx capturing sites that can significantly eliminate the release of toxic NO2(g) into the atmosphere. Using either (P1) or (P2) protocols, structurally different binary oxide systems can be synthesized enabling much superior photocatalytic total NOx removal (i.e. up to 176% higher) than Degussa P25. Furthermore, such binary oxides can also simultaneously decrease the toxic NO2(g) emission to the atmosphere by 75% with respect to that of Degussa P25. There is a complex interplay between calcination temperature, crystal structure, composition and specific surface area, which dictate the ultimate photocatalytic activity in a coordinative manner. Two structurally different photocatalysts prepared via different preparation protocols reveal comparably high photocatalytic activities implying that the active sites responsible for the photocatalytic NO(g) oxidation and storage have a non-trivial nature.
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    Lyotropic liquid-crystalline mesophases of [Zn(H2O)6](NO3)2-C12EO10-CTAB-H2O and [Zn(H2O)6](NO3)2-C12EO10-SDS-H2O systems
    (2008) Albayrak, C.; Soylu, A. M.; Dag, Ö.
    The mixture of two surfactants (C12EO10-CTAB and C 12EO10-SDS) forms lyotropic liquid-crystalline (LLC) mesophases with [Zn(H2O)6](NO3)2 in the presence of a minimum concentration of 1.75 H2O per C 12EO10. The metal ion/C12EO10 mole ratio can be increased up to 8.0, which is a record high metal ion density in an LLC mesophase. The metal ion concentration can be increased in the medium by increasing the CTAB/C12EO10 or SDS/C12EO 10 mole ratio at the expense of the stability of the LLC mesophase. The structure and some thermal properties of the new mesophase have been investigated using XRD, POM, FTIR, and Raman techniques. © 2008 American Chemical Society.
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    The role of charged surfactants in the thermal and structural properties of lyotropic liquid crystalline mesophases of [Zn(H2O)6](NO3)2-CnEOm-H2O
    (2010) Albayrak, C.; Soylu, A. M.; Dag, Ö.
    The mixtures of [Zn(H2O)6](NO3)2 salt, 10-lauryl ether (C12H25(OCH2CH2)10OH, represented as C12EO10), a charged surfactant (cetyltrimethylammonium bromide, C16H33N(CH3)3Br, represented as CTAB or sodium dodecylsulfate, C12H25OSO3Na, SDS) and water form lyotropic liquid crystalline mesophases (LLCM). This assembly accommodates up to 8.0 Zn(II) ions (corresponds to about 80% w/w salt/(salt + C12EO10)) for each C12EO10 in the presence of a 1.0 CTAB (or 0.5 SDS) and 3.5 H2O in its LC phase. The salt concentration can be increased by increasing charged surfactant concentration of the media. Addition of charged surfactant to the [Zn(H2O)6](NO3)2–C12EO10 mesophase not only increases the salt content, it can also increase the water content of the media. The charged surfactant-C12EO10 (hydrophobic tail groups) and the surfactant (head groups)-salt ion (ion-pair, hydrogen-bonding) interactions stabilize the mesophases at such salt high and water concentrations. The presence of both Br and NO 3 ions influences the thermal and structural properties of the [Zn(H2O)6](NO3)2–C12EO10–CTAB(or SDS)–H2O LLCM, which have been investigated using XRD, POM (with a hot stage), FT-IR and Raman techniques.
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    SOx uptake and release properties of TiO2/Al2O3 and BaO/TiO2/Al2O3 mixed oxide systems as NOx storage materials
    (Elsevier, 2012-04-30) Şentürk, G. S.; Vovk, E. I.; Zaikovskii, V. I.; Say, Z.; Soylu, A. M.; Bukhtiyarov, V. I.; Ozensoy, E.
    Titania was used as a promoter to obtain novel materials in the form of TiO2/Al2O3 (Ti/Al) and BaO/TiO2/Al2O3 (Ba/Ti/Al, containing 8 wt% or 20 wt% BaO) that are relevant to NOx storage reduction (NSR) catalysis. Two different protocols (P1, P2) were utilized in the synthesis. Ti/Al(P1) manifests itself as crystallites of TiO2 on -Al2O3, while Ti/Al(P2) reveals an amorphous AlxTiyOz mixed oxide. The structures of the synthesized materials were investigated via TEM, EDX, BET analysis and XPS while the catalytic functionality/performance of these support materials upon SOx and subsequent NOx adsorption were investigated with TPD and in situ FTIR spectroscopy. Ti/Al(P1, P2) revealed a high affinity towards SOx. Overall thermal stabilities of the adsorbed SOx species and the total SOx uptake of the Ba-free samples increase in the following order: TiO2(anatase) -Al2O3 < Ti/Al(P1) < Ti/Al(P2). The superior SOx uptake of Ti/Al(P1, P2) support materials can be tentatively attributed to the increasing specific surface area upon TiO2 promotion and/or the changes in the surface acidity. Promotion of BaO/Al2O3 with TiO2 leads to the attenuation of the SOx uptake and a significant decrease in the thermal stability of the adsorbed SOx species. The relative SOx adsorption capacities of the investigated materials can be ranked as follows: 8Ba/Ti/Al(P1) < 8Ba/Ti/Al(P2) < 8Ba/Al ∼ 20Ba/Ti/Al(P1) < 20Ba/Al < 20Ba/Ti/Al(P2).
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    TiO2-Al2O3 binary mixed oxide surfaces for photocatalytic NOx abatement
    (Elsevier, 2014) Soylu, A. M.; Polat, M.; Erdogan, D. A.; Say, Z.; Yıldırım, C.; Birer, Ö.; Ozensoy, E.
    TiO2-Al2O3 binary oxide surfaces were utilized in order to develop an alternative photocatalytic NOx abatement approach, where TiO2 sites were used for ambient photocatalytic oxidation of NO with O2 and alumina sites were exploited for NOx storage. Chemical, crystallographic and electronic structure of the TiO2-Al2O3 binary oxide surfaces were characterized (via BET surface area measurements, XRD, Raman spectroscopy and DR-UV-Vis Spectroscopy) as a function of the TiO2 loading in the mixture as well as the calcination temperature used in the synthesis protocol. 0.5 Ti/Al-900 photocatalyst showed remarkable photocatalytic NOx oxidation and storage performance, which was found to be much superior to that of a Degussa P25 industrial benchmark photocatalyst (i.e. 160% higher NOx storage and 55% lower NO2(g) release to the atmosphere). Our results indicate that the onset of the photocatalytic NOx abatement activity is concomitant to the switch between amorphous to a crystalline phase with an electronic band gap within 3.05-3.10 eV; where the most active photocatalyst revealed predominantly rutile phase together and anatase as the minority phase.