Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection

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

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  • Article
    Citation - WoS: 23
    Citation - Scopus: 23
    Use of Polyethylene Glycol Coatings for Optical Fibre Humidity Sensing
    (Springer Verlag, 2008) Açıkgöz, Sabriye; Bilen, Bukem; Demir, Mustafa Muammer; Menceloğlu, Yusuf Z.; Skarlatos, Yani; Aktaş, Gülen; İnci, Mehmet N.
    Humidity induced change in the refractive index and thickness of the polyethylene glycol (PEG) coatings are in situ investigated for a range from 10 to 95%, using an optical waveguide spectroscopic technique. It is experimentally demonstrated that, upon humidity change, the optical and swelling characteristics of the PEG coatings can be employed to build a plastic fibre optic humidity sensor. The sensing mechanism is based on the humidity induced change in the refractive index of the PEG film, which is directly coated onto a polished segment of a plastic optical fibre with dip-coating method. It is observed that PEG, which is a highly hydrophilic material, shows no monotonic linear response to humidity but gives different characteristics for various ranges of humidity levels both in index of refraction and in thickness. It undergoes a physical phase change from a semi-crystalline structure to a gel one at around 80% relative humidity. At this phase change point, a drastic decrease occurs in the index of refraction as well as a drastic increase in the swelling of the PEG film. In addition, PEG coatings are hydrogenated in a vacuum chamber. It is observed that the hydrogen has a preventing effect on the humidity induced phase change in PEG coatings. Finally, the possibility of using PEG coatings in construction of a real plastic fibre optic humidity sensor is discussed.
  • Article
    Citation - WoS: 47
    Effect of Filler Amount on Thermoelastic Properties of Poly (dimethylsiloxane) Networks
    (Elsevier Ltd., 2005) Demir, Mustafa Muammer; Menceloğlu, Yusuf Z.; Erman, Burak
    End-linked poly(dimethylsiloxane) (PDMS) networks were prepared in the presence of fumed silica particles with hydroxyl groups at their surfaces. The silica particles were introduced into the polymer solution prior to end-linking. Hydroxyl ended PDMS chains were end-linked via the tetra functional crosslinker, tetraethoxysilane. The filler content varied in the range 0-5 wt%. Atomic Force Microscopy was used to image and characterize the silica particles. Swelling, stress-strain and thermoelasticity experiments were performed. The temperature coefficient and the energetic part of the force in uniaxial extension are found to increase with increasing silica amount. This observation is ascribed to effects contributed possibly by the adsorption layer around the silica particles.
  • Article
    Citation - WoS: 263
    Palladium Nanoparticles by Electrospinning From Poly(acrylonitrile-Co Acid)-Pdcl2 Solutions. Relations Between Preparation Conditions, Particle Size, and Catalytic Activity
    (American Chemical Society, 2004) Demir, Mustafa Muammer; Gülgün, Mehmet A.; Menceloğlu, Yusuf Z.; Erman, Burak; Abramchuk, Sergei S.; Makhaeva, Elena E.; Khokhlov, Alexei R.; Matveeva, Valentina G.; Sulman, Mikhail G.
    Catalytic palladium (Pd) nanoparticles on electrospun copolymers of acrylonitrile and acrylic acid (PAN-AA) mats were produced via reduction of PdCl2 with hydrazine. Fiber mats were electrospun from homogeneous solutions of PAN-AA and PdCl2 in dimethylformamide (DMF). Pd cations were reduced to Pd metals when fiber mats were treated in an aqueous hydrazine solution at room temperature. Pd atoms nucleate and form small crystallites whose sizes were estimated from the peak broadening of X-ray diffraction peaks. Two to four crystallites adhere together and form agglomerates. Agglomerate sizes and fiber diameters were determined by scanning and transmission electron microscopy. Spherical Pd nanoparticles were dispersed homogeneously on the electrospun nanofibers, The effects of copolymer composition and amount of PdCl2 on particle size were investigated. Pd particle size mainly depends on the amount of acrylic acid functional groups and PdCl2 concentration in the spinning solution. Increasing acrylic acid concentration on polymer chains leads to larger Pd nanoparticles. In addition, Pd particle size becomes larger with increasing PdCl2 concentration in the spinning solution. Hence, it is possible to tune the number density and the size of metal nanoparticles. The catalytic activity of the Pd nanoparticles in electrospun mats was determined by selective hydrogenation of dehydrolinalool (3,7-dimethyloct-6-ene-l-yne-3-ol, DHL) in toluene at 90°C. Electrospun fibers with Pd particles have 4.5 times higher catalytic activity than the current PoVAl2O3 catalyst.
  • Article
    Citation - WoS: 30
    Citation - Scopus: 30
    Glycidyl-Methacry Late-Based Electrospun Mats and Catalytic Silver Nanoparticles
    (John Wiley and Sons Inc., 2008) Demir, Mustafa Muammer; Uğur, Gökçe; Gülgün, Mehmet A.; Menceloğlu, Yusuf Z.
    P(AN-GMA) and PGMA fibers coated with monodisperse silver nanoparticles have been prepared by a combination of electrospinning and electroless plating. The morphology of the electrospun fibers remains unchanged after surface hydrazination. Oxidation of hydrazine in an ammoniacal solution of AgNO 3 reduces and deposits silver atoms along the fiber surface, which then coalesce to Ag particles. The size of the silver nanoparticles is varied between 20-60 nm. Since the density of the active sites for silver reduction is lower in P(AN-GMA), a smaller particle size could be obtained. The catalytic activity of the silver nanoparticles has been confirmed.