Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
Browse
4 results
Search Results
Now showing 1 - 4 of 4
Article Citation - WoS: 1Citation - Scopus: 2A Molecularly Imprinted Polymer as Solid Phase Extraction Sorbent for Ketoprofen Determination in Water and Artificial Serum Prior To Hplc(TÜBİTAK - Türkiye Bilimsel ve Teknolojik Araştırma Kurumu, 2022) Shahwan, Talal; Gürel Özyurt, Elif; Özyurt, Ömer; Ölçer, Yekta Arya; Eroğlu, Ahmet Emin; Boyacı, EzelKetoprofen (KET) is an active pharmaceutical compound that has pain relieving and antipyretic effects. Its determination in body fluids and environmental waters is important due to widespread use of the compound. In this study, a selective and reliable method has been developed for the determination of ketoprofen in water and artificial serum using molecularly imprinted polymers (MIPs) as a solid phase extraction sorbent prior to HPLC-DAD detection. The MIP was synthesized by copolymerization of methacrylic acid (MAA) and trimethylpropane trimethacrylate (TRIM) in the presence of ketoprofen as the template. For the sake of comparison, nonimprinted polymer (NIP) was also synthesized under the same experimental conditions without the addition of ketoprofen under the same experimental conditions. Critical extraction parameters such as sample pH, shaking time and sorbent amount were optimized and adjusted to 8.0, 24 h, and 10.0 mg, respectively, for a sample volume of 10.0 mL. MIP showed higher selectivity than NIP towards ketoprofen in an artificial matrix containing another pain relieving drug, ibuprofen, and a cardiovascular drug, metoprolol. The proposed method was successfully applied for the detection of ketoprofen in spiked drinking water, tap water, and artificial serum samples, and showed satisfactory results with respective recoveries of 96.8 % (± 0.8), 93.7% (± 0.6), 62.2% (± 0.6), and 69.9% (± 0.6).Article Citation - WoS: 13Citation - Scopus: 15Synthesis of Poly-2 Methacrylate-Montmorillonite Nanocomposite Via in Situ Atom Transfer Radical Polymerization(Cambridge University Press, 2008) Oral, Ayhan; Shahwan, Talal; Güler, ÇetinThe poly-2-hyroxyethyl methacrylate (PHEMA)/clay nanocomposite was synthesized by in situ atom transfer radical polymerization (ATRP) from initiator moieties immobilized within the silicate galleries of the clay particles. To produce organically modified montmorillonite (MMT) that has ATRP initiator moiety, a new catalyst that consists of quaternary ammonium salt moiety and an initiator moiety was synthesized. This initiator was intercalated into the interlayer spacing of the MMT. The polymerization reaction was carried out in a mixed solvent system consisting of methyl ethyl ketone and 1-propanol at 50 °C, using the initiator that has been already synthesized with a copper bromide catalyst. The 2, 2′-bipyridyl (bpy) complex was used as ligand. The products were characterized via Fourier transform infrared, nuclear magnetic resonance (1H NMR, 12C NMR), transmission electron microscopy, x-ray diffraction, thermogravimetric analysis, and differential scanning calorimetry. © 2008 Materials Research Society.Article Citation - WoS: 21Citation - Scopus: 21Retention of Aqueous Ba2+ Ions by Calcite and Aragonite Over a Wide Range of Concentrations: Characterization of the Uptake Capacity, and Kinetics of Sorption and Precipitate Formation(The Geochemical Society of Japan, 2007) Tunusoğlu, Özge; Shahwan, Talal; Eroğlu, Ahmet EminThe uptake of aqueous Ba2+, ions by abiogenic calcite and aragonite was studied over a wide range of concentration; 1.0 × 101, 5.0 × 101, 1.0 × 102 5.0 × 102, 1.0 × 103, 5.0 × 104, and 1.0 × 104 mg/L. The uptake process was characterized using ICP-AES, XRPD, SEM/EDS, and FTIR techniques. Up to the initial concentration of 5.0 × 102 mg/L, the uptake of Ba2+ ions was fast and obeyed Lagergren's kinetic model. The equilibrium data were adequately described using Freundlich isotherm model. The overgrowth of BaCO3 (witherite) took place at higher concentrations, in a kinetically slow process and enhanced the uptake of Ba2+ ions. Quantitative XRPD was used to evaluate the fractions of precipitated BaCO3 on calcite and aragonite minerals and monitor their variation with time. At all the studied concentrations, aragonite showed higher removal capacity of Ba2+ and faster uptake kinetics than did calcite. The precipitated crystals appeared to predominantly possess olivary-like morphology with an average particle size of 1-2 μm. EDS was used to reveal the elemental quantities of Ba and Ca after BaCO3 formation on calcite and aragonite surfaces. FTIR spectroscopy was employed to analyze the vibrational modes in carbonate mixtures upon incorporation of Ba2+ by sorption and precipitation mechanisms.Article Citation - WoS: 11Citation - Scopus: 13Study of the Scavenging Behavior and Structural Changes Accompanying the Interaction of Aqueous Pb2+ and Sr2+ Ions With Calcite(The Geochemical Society of Japan, 2005) Shahwan, Talal; Zünbül, B.; Akar, DilekThe uptake of Pb2+ and Sr2+ ions from aqueous solutions by calcite was studied at various initial concentrations and pH conditions using the batch method under ambient conditions. XRPD, SEM/ EDS, AAS/AES, and DRIFT techniques were used in characterizing the sorption process. The results indicated that the retention mechanism of Ph2+ and Sr2+ ions ranged from ion incorporation to precipitate overgrowth (cerussite, hydrocerussite for Pb, strontianite for Sr) depending on the concentration and pH conditions. The calcite structure seemed to be entirely vanishing upon formation of cerussite and hydrocerussite while partial dissolution of calcite occurred upon strontianite formation. The formation of precipitates showed rapid kinetics, and equilibrium seemed to be reached within about an hour from the start of mixing. SEM analysis showed that cerussite, hydrocerussite, and strontianite had columnar prismatic-like, tabular hexagonal-like, and needle-like morphologies. Based on a nine-month observation period, dry samples of hydrocerussite seemed to show more morphological stability than cerussite. EDS analysis indicated that Pb2+ sorption is more favored than that of Sr2+, particularly in the phase of precipitate overgrowth. DRIFT analysis indicated a change in the symmetry of the carbonate groups in calcite matrix upon uptake of Pb2+ and Sr2+ cations.
