Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
Browse
6 results
Search Results
Now showing 1 - 6 of 6
Article Citation - WoS: 8Citation - Scopus: 10Trypsin-Immobilized Silica: a Novel Adsorbent for V(iv) and V(v) Removal From Water(Water Environment Federation, 2018) Erdem Yayayürük, Aslı; Shahwan, Talal; Şanlı Mohamed, Gülşah; Eroğlu, Ahmet EminIn the present study, trypsin-immobilized silica was employed for the removal of V(IV) and V(V) ions from water. The synthesized sorbent was first characterized and then investigated for the removal of V(IV) and V(V) under various experimental conditions. The adsorption performance of the sorbent was tested as a function of pli, sorbent amount, initial vanadium concentration, contact time, and temperature. The sorption process was then investigated, both from a kinetic perspective and also in terms of isotherm models. The Langmuir adsorption isotherm was the best model to describe the sorption process. Sorption thermodynamics were spontaneous and exothermic. The proposed method was successfully applied to real samples for the removal of V(IV)and V(V) with sufficient accuracy and precision.Article Citation - WoS: 69Citation - Scopus: 77Morphosynthesis of Caco3 at Different Reaction Temperatures and the Effects of Pdda, Ctab, and Edta on the Particle Morphology and Polymorph Stability(Elsevier Ltd., 2007) Altay, E.; Shahwan, Talal; Tanoğlu, MetinFacile precipitation of CaCO3 was performed using aqueous solutions of CaCl2 with Na2CO3 over a wide range of mixing and aging temperatures. The precipitation process was then repeated in the presence of PDDA, CTAB, and EDTA at the mixing temperatures of 30 °C, 50 °C, 70 °C, and 90 °C. The presence of these additives was seen to greatly suppress the formation of aragonite. Among these additives, EDTA was the one that showed the most prominent effects on particle morphology of CaCO3. The sequence of pH adjustment appeared to be a critical factor for the additive functionality.Article Citation - WoS: 19Citation - Scopus: 21Kinetic and Thermodynamic Investigations of Strontium Ions Retention by Natural Kaolinite and Clinoptilolite Minerals(Walter De Gruyter Gmbh, 2005) Akar, Dilek; Shahwan, Talal; Eroğlu, Ahmet EminThe current study was devoted to the determination of various thermodynamic and kinetic parameters resulting from the fixation of Sr2+ by natural samples of kaolinite and clinoptilolite minerals. The sorption process followed pseudo second order kinetics, with faster sorption on kaolinite compared to clinoptilolite, where the uptake is affected by intraparticle diffusion. Freundlich and Dubinin-Radushkevich isotherm models described the data more adequately than Langmuir model, and clinoptilolite showed a higher strontium sorption capacity than kaolinite. Thermodynamically, the activation energy of Sr2+ sorption by kaolinite and clinoptilolite were respectively, -8.5 and -18.4 kJ/mol. The sorption process on both minerals was spontaneous and endothermic at all the studied concentrations, with ΔH° being 11.3 and 9.8 kJ/mol, for sorption on kaolinite and clinoptilolite, respectively. The findings of this study were compared with those of an earlier study on the uptake of Cs+ by the same minerals.Article Citation - WoS: 27Citation - Scopus: 29Characterization of Sr2+ Uptake on Natural Minerals of Kaolinite and Magnesite Using Xrpd, Sem/Eds, Xps, and Drift(Walter De Gruyter Gmbh, 2005) Shahwan, Talal; Erten, Hasan N.The sorption behavior of Sr2+ ions on natural minerals rich in kaolinite and magnesite was studied using SEM/EDS, XPS, XRPD, AAS/AES and DRIFT techniques. Quantitative analysis of the XPS data shows that magnesite is more effective in Sr2+ uptake than kaolinite. DRIFT spectra and XRPD patterns indicate that the structures of both minerals were not affected upon Sr2+ sorption. Intercalation of DMSO in kaolinite lamellae aiming at increasing the interlayer space did not significantly enhance the sorption capacity of the clay towards Sr2+ probably due to the lack of a negative charge on the accessible sites. EDS mapping indicated that while the sorbed Sr is equally distributed on surface of natural kaolinite, it was associated - to a larger extent - with the regions richer in Mg in the case of natural magnesite. Comparing the uptake mechanisms of natural magnesite with that of pure MgCO3, it was seen that while natural magnesite sorbed Sr2+ mainly through an ion exchange type mechanism, the formation of SrCO3 coprecipitate was detected on the surface of the MgCO 3 at higher loadings.Article Citation - WoS: 109Citation - Scopus: 124Chitosan Fiber-Supported Zero-Valent Iron Nanoparticles as a Novel Sorbent for Sequestration of Inorganic Arsenic(Royal Society of Chemistry, 2013) Horzum Polat, Nesrin; Demir, Mustafa Muammer; Nairat, Muath; Shahwan, TalalThis study proposes a new sorbent for the removal of inorganic arsenic from aqueous solutions. Monodispersed nano zero-valent iron (nZVI) particles were nucleated at the surface of electrospun chitosan fibers (average fiber diameter of 195 ± 50 nm) by liquid phase reduction of FeCl3 using NaBH4. The material was characterized using SEM, TGA, XPS, XRD, and FTIR. The diameter of iron nanoparticles was found to vary between 75-100 nm. A set of batch experiments were carried out to elucidate the efficiency of the composite sorbent toward fixation of arsenite and arsenate ions. The ion concentrations in the supernatant solutions were determined using inductively coupled plasma-mass spectrometry (ICP-MS). The results revealed that the chitosan fiber supported nZVI particles is an excellent sorbent material for inorganic arsenic uptake at concentrations ranging from 0.01 to 5.00 mg L -1 over a wide range of pH values. Based on XPS analysis, As(iii) was found to undergo oxidation to As(v) upon sorption, while As(v) retained its oxidation state. By virtue of the successful combination of the electrospun fibers' mechanical integrity and the large reactivity of dispersed nZVI particles, the applicability of the resulting sorbent material in arsenic sorption holds broad promise.Article Citation - WoS: 119Citation - Scopus: 151Batch Removal of Aqueous Cu2+ Ions Using Nanoparticles of Zero-Valent Iron: a Study of the Capacity and Mechanism of Uptake(American Chemical Society, 2008) Karabelli, Duygu; Üzüm, Çağrı; Shahwan, Talal; Eroğlu, Ahmet Emin; Scott, Tom B.; Hallam, Keith R.; Lieberwirth, IngoIn this study, nZVI prepared by borohydride reduction was applied for the removal of Cu2+ ions under a variety of experimental conditions. The uptake experiments investigated the effects of initial concentration, contact time, pH, and repetitive loading on the extent of retardation of Cu2+ ions. Within the applied conditions, the sorbent demonstrated fast uptake kinetics and outstanding fixation abilities up to an initial Cu2+ concentration of 200.0 mg/L. Partitioning of Cu2+ ions between liquid and solid phases demonstrated an isotherm of L-type. Within the studied conditions, the capacity of uptake was found to be 250 mg of Cu2+ per g of nZVI. According to X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) results, Cu2+ ions were sorbed primarily via a redox mechanism that resulted in the formation of Cu2O and Cu0. The contact of iron nanoparticles with aqueous media caused extensive formation of iron oxide. However, the material did not completely lose its removal capacity and was repeatedly applied at low concentrations for further uptake trials.