Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article A Simplified Molecular Imprinting Strategy Through Electrospinning of Polyacrylonitrile for Thin Film Microextraction of Selected Pesticides(Elsevier B.V., 2026) Şahin, A.; Akpinar, Y.; Yildirim, E.; Eroǧlu, A.E.; Boyaci, E.Molecularly imprinted polymers (MIPs) have been extensively used as selective extractive phases for sample preparation because of their analyte-selective binding sites. However, MIP preparation requires optimized monomer-template interactions and long polymerization reactions. In this study, a novel and simple method of MIP preparation was proposed based on electrospinning. Instead of preparing analyte-monomer complexes before polymerization, model analytes (trifluralin and carbaryl) were directly dissolved in a polyacrylonitrile (PAN) solution, then electrospun into nanofibrous mats. This allowed for a means of preparation of highly crystalline, template-imprinted nanostructures with minimal synthetic complexity. Following the characterization studies for the new material, the extraction properties of the imprinted and nonimprinted electrospun mats were investigated in thin film microextraction (TFME) studies by extracting trifluralin and carbaryl from water samples, followed by gas chromatography-mass spectrometry (GC–MS) analysis. The optimization results showed that samplers containing 10.0 mg of MIP sorbents made by electrospinning of a solution containing 5.0 mg of template in 1.0 mL of PAN solution resulted in approximately 4 and 7 times enhanced extraction recoveries for carbaryl and trifluralin compared to samplers made of non-imprinted bulk PAN. Moreover, the cross-reactivity testing performed with non-template analytes (malathion and diazinon) suggested a more specific extraction towards trifluralin compared to carbaryl. The proposed new technique was also validated using computational methodology, which supported the experimental finding about higher selectivity towards trifluralin. This may signify a probability for structural orientation of partially charged trifluralin under an electrical field in electrospun PAN creating favorable extraction sites. © 2025 Elsevier B.V.Article Citation - WoS: 50Citation - Scopus: 55Determination of Henry's Law Constants of Organochlorine Pesticides in Deionized and Saline Water as a Function of Temperature(Elsevier Ltd., 2006) Çetin, Banu; Özer, Serdar; Sofuoğlu, Aysun; Odabaşı, MustafaThe Henry's law constant (H) is an important parameter that is required to estimate the air-water exchange of semi-volatile organic compounds. Henry's law constants for 17 banned/restricted/currently used organochlorine pesticides (OCPs) were experimentally determined using a gas-stripping technique in deionized and saline water (3%) over a temperature range of 5-35 °C. H values (at 25 °C) ranged between 0.066±0.037 Pa m3 mol-1 (endosulfan II) and 62.0±24.2 Pa m3 mol-1 (heptachlor) in deionized water while the range in saline water was 0.28±0.03 Pa m3 mol-1 (γ-HCH) and 135.2±31.3 Pa m3 mol-1 (heptachlor). The increase in dimensionless Henry's law constants (H′) for OCPs over the studied temperature range was between 3 (γ-HCH)-19 times (chlorpyrifos) and 3 (endosulfan II)-80 times (trans-nonachlor) in deionized and saline water, respectively. The calculated enthalpies of phase change (ΔHH) were within the ranges previously reported for OCPs and other organic compounds (23.8-100.2 kJ mol-1). The salting-out constant, ks, ranged between 0.04 (γ-HCH) and 1.80 L mol-1 (endosulfan II) indicating the importance of assessing the H values of OCPs in saline water to accurately determine their partitioning and fate in seawater.Article Determination of Henry's Law Constants of Organochlorine Pesticides in Deionized and Saline Water as a Function of Temperature(Elsevier Ltd., 2006) Çetin, Banu; Özer, Serdar; Sofuoğlu, Aysun; Odabaşı, MustafaThe publisher regrets that the second paragraph on p. 4545 was printed incorrectly. It now appears correctly, below. The presence of salts in aqueous solution affects the solubility of organic molecules, through the salting-out effect (Demou and Donaldson, 2002). The salting-out is defined as the decrease in aqueous solubility and increase in the activity coefficient observed for neutral non-polar compounds by dissolved inorganic salts. Ions in solution tightly bind several water molecules into hydration shells. This process (electrostriction), results in a reduction of the volume of the aqueous solution. A smaller aqueous volume results in less available water for cavity formation, and therefore less organic molecules are accommodated; their solubility decreases as a consequence (Schwarzenbach et al., 2002; Demou and Donaldson, 2002). The empirical relation for the effect of ionic strength on Henry’s law constant is described by Setschenow equation (Demou and Donaldson, 2002):