Browsing by Subject "Spectrometry"
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Item Open Access All-chalcogenide variable infrared filter(SPIE, 2009) Kondakcı, H. Esat; Köyle, Özlem; Yaman, Mecit; Dana, Aykutlu; Bayındır, MehmetWe present the design, fabrication, characterization of spatially variable infrared filter and a demonstration of the filter as a simple infrared spectrometer. A varying photonic band gap filter which consists of thermally evaporated, high refractive index contrast amorphous chalcogenide glass multilayers, makes the structure suitable to be used as spectrometer. Due to graded thickness structure, the filter exhibits a position dependent stop band and a cavity mode ranging from 2 to 8 μm wavelengths. It is demonstrated that the filter can be used to detect absorption peaks of common gases in the cavity mode range of the filter. © 2009 SPIE.Item Open Access Cyclodextrin functionalized poly(methyl methacrylate) (PMMA) electrospun nanofibers for organic vapors waste treatment(Elsevier BV, 2010) Uyar, Tamer; Havelund, R.; Nur, Y.; Balan, A.; Hacaloglu, J.; Toppare, L.; Besenbacher, F.; Kingshott, P.Poly(methyl methacrylate) (PMMA) nanofibers containing the inclusion complex forming betacyclodextrin (_-CD) were successfully produced by means of electrospinning in order to develop functional nanofibrous webs for organic vapor waste treatment. Electrospinning of uniform PMMA nanofibers containing different loadings of _-CD (10%, 25% and 50% (w/w)) was achieved. The surface sensitive spectroscopic techniques; X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS) showed that some of the _-CD molecules are present on the surface of the PMMA nanofibers, which is essential for the trapping of organic vapors by inclusion complexation. Direct pyrolysis mass spectrometry (DP-MS) studies showed that PMMA nanowebs containing _-CD can entrap organic vapors such as aniline, styrene and toluene from the surroundings due to inclusion complexation with _-CD that is present on the fiber surface. Our study showed that electrospun nanowebs functionalized with cyclodextrinsmayhave the potential to be used as molecular filters and/or nanofilters for the treatment of organic vapor waste and air filtration purposes.Item Open Access Functional electrospun polystyrene nanofibers incorporating α-, β-, and γ-cyclodextrins: Comparison of molecular filter performance(2010) Uyar, Tamer; Havelund, R.; Hacaloglu, J.; Besenbacher, F.; Kingshott, P.Electrospinning has been used to successfully create polystyrene (PS) nanofibers containing either of three different types of cyclodextrin (CD); α-CD, β-CD, and γ-CD. These three CDs are chosen because they have different sized cavities that potentially allow for selective inclusion complex (IC) formation with molecules of different size or differences in affinity of IC formation with one type of molecule. The CD containing electrospun PS nanofibers (PS/CD) were initially characterized by scanning electron microscopy (SEM) to determine the uniformity of the fibers and their fiber diameter distributions. X-ray photoelectron spectroscopy (XPS) was used to quantitatively determine the concentration of each CD on the different fiber surfaces. Static time-of-flight secondary ion mass spectrometry (static-ToF-SIMS) showed the presence of each type of CD on the PS nanofibers by the detection of both the CD sodium adduct molecular ions (M + Na+) and lower molecular weight oxygen containing fragment ions. The comparative efficiency of the PS/CD nanofibers/nanoweb for removing phenolphthalein, a model organic compound, from solution was determined by UV-vis spectrometry, and the kinetics of phenolphthalein capture was shown to follow the trend PS/α-CD > PS/β-CD > PS/γ-CD. Direct pyrolysis mass spectrometry (DP-MS) was also performed to ascertain the relative binding strengths of the phenolphthalein for the CD cavities, and the results showed the trend in the interaction strength was β-CD > γ-CD > α-CD. Our results demonstrate that nanofibers produced by electrospinning that incorporate cyclodextrins with different sized cavities can indeed filter organic molecules and can potentially be used for filtration, purification, and/or separation processes. © 2010 American Chemical Society.Item Open Access Investigation of binding properties of dicationic styrylimidazo[1,2-a]pyridinium dyes to human serum albumin by spectroscopic techniques(John Wiley and Sons Ltd, 2017) Özdemir, A.; Gökoğlu, E.; Yılmaz, Esra; Yalçın, E.; Gökoğlu, E.; Seferoğlu, Z.; Tekinay, T.The binding interaction between two dicationic styrylimidazo[1,2-a]pyridinium dyes and human serum albumin (HSA) was investigated at physiological conditions using fluorescence, UV–vis absorption, and circular dichroism (CD) spectroscopies. Analysis of the fluorescence titration data at different temperatures suggested that the fluorescence quenching mechanism of HSA by these dyes was static. The calculated thermodynamic parameters (ΔG°, ΔH° and ΔS°) indicated that hydrogen bonding and van der Waals forces played a major role in the formation of the dye–HSA complex. Binding distances (r) between dyes and HSA were calculated according to Förster's non-radiative energy transfer theory. Studies of conformational changes of HSA using CD measurements indicate that the α-helical content of the protein decreased upon binding of the dyes.Item Open Access Photocatalytic conversion of nitric oxide on titanium dioxide: cryotrapping of reaction products for online monitoring by mass spectrometry(American Chemical Society, 2016) Lu, W.; Olaitan, A. D.; Brantley, M. R.; Zekavat, B.; Erdogan, D. A.; Ozensoy, E.; Solouki, T.Details of coupling a catalytic reaction chamber to a liquid nitrogen-cooled cryofocuser/triple quadrupole mass spectrometer for online monitoring of nitric oxide (NO) photocatalytic reaction products are presented. Cryogenic trapping of catalytic reaction products, via cryofocusing prior to mass spectrometry analysis, allows unambiguous characterization of nitrous oxide (N2O) and nitrogen oxide species (i.e., NO and nitrogen dioxide (NO2)) at low concentrations. Results are presented, indicating that the major photocatalytic reaction product of NO in the presence of titanium dioxide (TiO2) P25 and pure anatase catalysts when exposed to ultraviolet (UV) light (at a wavelength of 365 nm) is N2O. However, in the presence of rutile-rich TiO2 catalyst and UV light, the conversion of NO to N2O was less than 5% of that observed with the P25 or pure anatase TiO2 catalysts.Item Open Access Photonic bandgap infrared spectrometer(Optical Society of America, 2010) Kondakci, H.E.; Yaman, M.; Dana, A.; Bayındır, MehmetWe propose and demonstrate an infrared (IR) absorption spectrometer, made with a spatially variable photonic bandgap (PBG) structure, a blackbody source, and a simple IR detector, to identify the IR molecular fingerprints of analyte molecules. The PBG-based structure consists of thermally evaporated, IR transparent, high-refractive-index chalcogenide quarter-wave stacks (QWS) with a cavity layer. Spatial variation of the very sharp transmission peak due to the QWS cavity mode allows the structure to be used as a variable IR filter. Our proposed IR-PBG spectrometer can be used for detection and identification of volatile organic compounds.Item Open Access X-ray photoelectron spectroscopic characterization of Au collected with atom trapping on silica for atomic absorption spectrometry(Sage Publications, Inc., 1997) Süzer, Ş.; Ertaş, N.; Kumser, S.; Ataman, O. Y.The nature of analyte species collected on a cooled silica tube for atom-trapping atomic absorption spectrometric determination was investigated with the use of X-ray photoelctron spectroscopy (XPS). An XPS spectrum of gold deposited on atom-trapping silica tubes reveals a Au 4f7/2 peak with a binding energy of 84.8 (±0.2) eV, which falls in the middle of the binding energies corresponding to zerovalent Au(0) at 84.0 eV and that of monovalent Au(I) at 85.2 eV. The corresponding energy for Au vapor deposited on silica is also 84.8 eV. Deposition of AuCl4- solution on silica results in two different Au 4f7/2 peaks with binding energies of 84.8 and 87.3 eV corresponding, respectively, to Au(0) and Au(III). Deposition of the same AuCl4- solution on platinum metal again gives two peaks, this time at 84.4 and 87.0 eV energies corresponding again to Au(0) and Au(III). Combining all these data, we conclude that gold is trapped on atom-trapping silica surface as zerovalent Au(0) with a 0.8-eV matrix shift with respect to the metal surface. A similar 0.6-eV shift is also observed between the binding energy of 4f7/2 Hg22+ measured in Hg2(NO3)2·2H2O powder and that deposited on silica.