Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
Browse
7 results
Search Results
Other Erratum To: Mbe-Grown Cdte Layers on Gaas With In-Assisted Thermal Deoxidation(Springer Verlag, 2016) Arı, Ozan; Bilgilisoy, Elif; Özçeri, Elif; Selamet, YusufArticle Citation - WoS: 6Citation - Scopus: 5Mbe-Grown Cdte Layers on Gaas With In-Assisted Thermal Deoxidation(Springer Verlag, 2016) Arı, Ozan; Bilgilisoy, Elif; Özçeri, Elif; Selamet, YusufMolecular beam epitaxy (MBE) growth of thin (∼2 μm) CdTe layers characterized by high crystal quality and low defect density on lattice mismatched substrates, such as GaAs and Si, has thus far been difficult to achieve. In this work, we report the effects of in situ thermal deoxidation under In and As4 overpressure prior to the CdTe growth on epiready GaAs(211)B wafers, aiming to enhance CdTe crystal quality. Thermally deoxidized GaAs samples were analyzed using in situ reflection high energy electron diffraction, along with ex situ x-ray photo-electron spectroscopy (XPS) and atomic force microscopy. MBE-grown CdTe layers were characterized using x-ray diffraction (XRD) and Everson-type wet chemical defect decoration etching. We found that In-assisted desorption allowed for easier surface preparation and resulted in a smoother surface compared to As-assisted surface preparation. By applying In-assisted thermal deoxidation to GaAs substrates prior to the CdTe growth, we have obtained single crystal CdTe films with a CdTe(422) XRD rocking curve with a full-width half-maximum value of 130.8 arc-s and etch pit density of 4 × 106 cm−2 for 2.54 μm thickness. We confirmed, by XPS analysis, no In contamination on the thermally deoxidized surface.Article Citation - WoS: 19Citation - Scopus: 21Microwave Effect on Ion-Exchange and Structure of Clinoptilolite(Springer Verlag, 2007) Akdeniz, Yelda; Ülkü, SemraThe effect of microwave irradiation on the ion exchange degree and structure of clinoptilolite mineral has been examined in comparison with the conventional heat treatment in waterbath. Clinoptilolite-rich mineral from the Western Anatolia, Bigadiç region was used for the experimental study. The mineral was mainly clinoptilolite (80-85%) and additionally, quartz (5-10%), and analcime+mordenite (<5%) were found as co-existing minerals. The mineral was stable towards dehydration and maintains its original structure up to 800°C. The BET and Langmuir surface areas of the sample were found to be 22 and 17m2/g for N2 adsorption and 28 and 22m2/g for Ar adsorption, respectively. For the exchange experiments, clinoptilolite rich mineral was treated with 1N NaCl salt solution both in a microwave unit and waterbath for 10min, 1h and 2h at 80°C. The waterbath treatment with the same conditions was continued for two additional weeks. The chemical composition of the parent and Na-exchanged forms of the clinoptilolite rich minerals were analyzed by using Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES). Microwave treatment was found to be more rapid and effective for ion exchange compared to conventional waterbath treatment. Additionally, the XRD results reveal that microwave irradiation has zero effect on the structure of the clinoptilolite rich mineral.Article Citation - WoS: 30Citation - Scopus: 35Effect of Temperature and Time on Zinc Borate Species Formed From Zinc Oxide and Boric Acid in Aqueous Medium(American Chemical Society, 2007) Eltepe, H. Emre; Balköse, Devrim; Ülkü, SemraThe effect of temperature and time of heating of zinc oxide and boric acid in aqueous medium on product type, dehydration behavior, crystal morphology, and structure was investigated for the production of flame retardant and smoke suppressant zinc borate. Two different products dehydrated at 140 and 350°C were obtained and characterized by thermal gravimetric analysis, X-ray diffraction, energy dispersive spectroscopy, and Fourier transform infrared spectroscopy.Article Citation - WoS: 11Citation - Scopus: 13Liquid-Phase Oxidation of Carvacrol Using Zeolite-Encapsulated Metal Complexes(American Chemical Society, 2006) Güneş, Alev; Bayraktar, Oğuz; Yılmaz, SelahattinWe 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: 19Citation - Scopus: 19Biofilm Formation by Staphylococcus Epidermidis on Nitrogen Ion Implanted Cocrmo Alloy Material(John Wiley and Sons Inc., 2007) Öztürk, Orhan; Sudağıdan, Mert; Türkan, UğurStaphylococcus epidermidis is the primary cause of medical device-related infections due to its adhesion and biofilm forming abilities on biomaterial surfaces. For this reason development of new materials and surfaces to prevent bacterial adhesion is inevitable. In this study, the adhesion of biofilm forming S. epidermidis strain YT-169a on nitrogen (N) ion implanted as well as on as-polished CoCrMo alloy materials were investigated. A medical grade CoCrMo alloy was ion implanted with 60 keV N ions to a high dose of 1.9 × 10 18 ions/cm2 at substrate temperatures of 200 and 400°C. The near-surface implanted layer crystal structures, implanted layer thicknesses, and roughnesses were characterized by XRD, SEM and AFM. The number of adherent bacteria on the surfaces of N implanted specimens was found to be 191 × 106 CFU/cm2 for the 200°C and 70 × 106 CFU/cm2 for the 400°C specimens compared to the as-polished specimen (3 × 106 CFU/cm2). The adhesion test results showed that S. epidermidis strain YT-169a adhere much more efficiently to the N implanted surfaces than to the as-polished CoCrMo alloy surface. This was attributed mainly to the rougher surfaces associated with the N implanted specimens in comparison with the relatively smooth surface of the as-polished specimen.Article Citation - WoS: 11Citation - Scopus: 12Hydrothermal Synthesis, Characterization and Magnetic Properties of Navge2o6 and Livge2o6(Elsevier Ltd., 2004) Eanes, Mehtap; Kolis, Joseph W.Supercritical fluids are shown to be an excellent reaction media for the synthesis of novel solid state phases at intermediate temperatures. LiVGe 2O6 and NaVGe2O6 have the common pyroxene structure composed of VO6 linear chains. NaVGe 2O6 crystallizes in the monoclinic space group C2/c with four formula units having cell dimensions a = 9.960(4)Å, b = 8.853(10)Å, c = 5.4861(10)Å, β = 106.403(3)°. The structure was refined until R = 0.0290 and Rw = 0.0370. For LiVGe 2O6 in space group P21/c: a = 9.8508(7)Å, b = 8.754(3)Å, c = 5.3948(13)Å, β = 108(3)°, R = 0.0240 and Rw = 0.0250. The compounds contain edge-shared VO6 octahedral chains and corner-shared GeO4 tetrahedral chains. The presence of these VO6 chains results in spin-Peierls distortion. Structural and physical characterization of the compounds are reported.