Chemical Engineering / Kimya Mühendisliği

Permanent URI for this collectionhttps://hdl.handle.net/11147/14

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  • Article
    Citation - WoS: 16
    Citation - Scopus: 13
    Energy storage performance of nitrogen-doped reduced graphene oxide/co-doped polyaniline nanocomposites
    (Springer, 2022) Altınışık, Hasan; Getiren, Bengü; Çıplak, Zafer; Soysal, Furkan; Yıldız, Nuray
    The design and exploration of carbon-based electrode materials have become highly significant for developing supercapacitor technology, which has attracted considerable attention in energy storage systems. Here, nitrogen-doped reduced graphene oxide (N-rGO) – Polyaniline (PANI) nanocomposites were synthesized by a facile two-step method in which in situ polymerization of aniline monomer was performed on hydrothermally synthesized N-rGO nanosheets in DBSA and H2SO4 medium for co-doping of PANI chains. The effects of various acid concentrations (DBSA:H2SO4 0.5 − 0.25:1 n/n) and N-rGO:aniline ratios (N-rGO:aniline 1:4–10 m/m) used in the preparation of the electrode material on the capacitive properties were investigated. It is found that the co-doped N-rGO-PANI nanocomposites exhibit a high specific capacitance of 346.3 F g− 1 at 1 A g− 1, remarkable rate capacity (99.9%, 1–10 A g− 1) and excellent cycle stability at 5 A g− 1 (81.3%, 5000 cycles) in a two-electrode system. As a result, constructing co-doped PANI chains and N-doped rGO provided a viable and simple way to improve the capacitive performances of supercapacitors.
  • Article
    Citation - WoS: 4
    Citation - Scopus: 4
    Polymer-Bonded Cdte Quantum Dot-Nitroxide Radical Nanoprobes for Fluorescent Sensors
    (Springer, 2022) Karabıyık, Merve; Ebil, Özgenç
    A novel functional polymer-bonded quantum dots (QDs)-nitroxide radical complex was demonstrated. In the first part of the study, the synthesis of polymer thin films via initiated chemical vapor deposition (iCVD), functionalization of polymer thin films with amine functional groups, and attachment of QDs to polymer surface were demonstrated. Fourier transform infrared spectroscopy and energy-dispersive X-ray spectroscopy together with fluorescence spectroscopy studies revealed that aliphatic primary amine (propylamine) was very effective for the functionalization of iCVD deposited poly(glycidyl methacrylate) (pGMA) and its copolymer with diethylaminoethyl methacrylate (p(GMA-co-DEAEMA)) and also QD attachment to functionalized polymer surface. In the second part of the study, the synthesis and attachment of Quantum Dot-4Amino TEMPO (QD-4AT) nanoprobes to functionalized pGMA thin films and feasibility of using them as fluorescent sensor structures were investigated. It was found that high initial 4AT concentration and long (24 h) interaction times are beneficial for nanoprobe synthesis. Electron paramagnetic resonance (EPR) spectroscopy analysis revealed the existence of covalent bond between QD and 4AT when 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide was used during synthesis. EPR analysis together with fluorescence microscopy investigation confirmed the successful attachment of nanoprobes to polymer surface. Time-depended fluorescence quenching analysis revealed that more than 50% reduction in fluorescence intensity within 15 min demonstrating the potential of polymer bonded QD-4AT nanoprobes in various sensor applications.
  • Article
    Citation - WoS: 13
    Citation - Scopus: 11
    Valorization of Olive Tree Pruning Waste for Potential Utilization in Lithium Recovery From Aqueous Solutions
    (Springer, 2022) Nampeera, Jackline; Recepoğlu, Yaşar Kemal; Yüksel, Aslı
    Olive tree pruning waste, mainly composed of olive branches, was converted into a value-added and sustainable product capable of lithium as a biosorbent through alkali treatment and phosphorylation reaction. Characterization studies were performed by SEM–EDX, XPS, FTIR, and TGA. Factors affecting biosorption mechanism, i.e., sorbent dosage, pH, initial Li+ concentration and temperature, and competitive ions’ presence, were investigated the synthesized functionalized olive branches (FOB). A commercial lithium selective resin, Lewatit TP 260, was also compared with FOB in batch and column studies. The Freundlich model fits adsorption isotherms better than the Langmuir model, with a maximum adsorption capacity of 6.7 mg/g at 30 °C and pH 7–8. Kinetic studies proved fast kinetics and equilibrium were attained in 6 min, while thermodynamic studies showed an exothermic (Δ Ho= - 17.52 kJ/ mol) , spontaneous reaction Δ Go< 0 at all temperatures), and increased randomness Δ So= + 24.27 J/ mol. K) at the interaction interface. Column studies revealed that although Lewatit TP 260 resin showed higher sorption capacity, its desorption efficiency (50.42%) was lower than that of FOB (99.9%), and the degree of column utilization of FOB (56.81%) was better than Lewatit TP 260 resin’s (16.0%). The findings were encouraging in the successful synthesis of a promising biosorbent from an abundant waste in Turkey for use in sustainable lithium recovery from aqueous sources. Graphical abstract: [Figure not available: see fulltext.]
  • Article
    Citation - WoS: 5
    Citation - Scopus: 5
    Novel Biopolymer-Based Hydrogels Obtained Through Crosslinking of Keratose Proteins Using Tetrakis(hydroxymethyl) Phosphonium Chloride
    (Springer, 2022) Yalçın, Damla; Top, Ayben
    Merino wool obtained from the Karacabey region of Turkey was solubilized using peracetic acid oxidation. The wool and extracted wool proteins (keratose) were characterized using SEM, XRD, TGA, and FTIR analyses. SDS-PAGE result of the keratose indicated diffusive bands were populated between ~ 40 and ~ 55 kDa, corresponding to low-sulfur content α-keratose proteins. Chemically crosslinked hydrogels were prepared using the keratose and tetrakis(hydroxymethyl) phosphonium chloride (THPC). Storage moduli of the hydrogels prepared at 1:1, 1:2, and 1:4 keratose to THPC reactive group ratios were measured as 63 ± 22, 291 ± 21, and 804 ± 53 Pa, respectively. Crosslinking degrees of the hydrogels also affected the secondary structures of the keratose films obtained from the drying of the hydrogels. The hydrogel with the highest crosslinking density (1:4 gel) exhibited the lowest swelling ratio, whereas the one with the lowest crosslinking density (1:1 gel) disintegrated in deionized water within less than 6 h. CCK-8 tests using L929 mouse fibroblast cells showed that all the hydrogels promoted cell proliferation. These results suggest THPC crosslinked hydrogels prepared at the millimolar THPC concentrations are biocompatible scaffolds, which can be utilized in drug delivery and tissue engineering applications. Graphical abstract: [Figure not available: see fulltext.]