Scopus İndeksli Yayınlar Koleksiyonu
Permanent URI for this collectionhttps://hdl.handle.net/20.500.12573/395
Browse
3 results
Search Results
Article Citation - WoS: 65Citation - Scopus: 71Preparation of Polyacrylamide Titanium Dioxide Hybrid Nanocomposite by Direct Polymerization and Its Applicability in Removing Crystal Violet From Aqueous Solution(Springer, 2023-08-02) Arslan, Dilek Senol; Ertap, Hueseyin; Senol, Zeynep Mine; El Messaoudi, Noureddine; Mehmeti, ValboneThe present paper focused on synthesizing a polyacrylamide-titanium dioxide (PAA@TiO2) nanocomposite using a cross-linking method with N, N & PRIME;-methylenebisacrylamide and then using this composite to eliminate crystal violet (CV) dye from water and to characterize the adsorbent by XRD, FT-IR, and SEM-EDX techniques. The characterization revealed that TiO2 nanoparticles dispersed homogeneously within the polymer matrix. The maximum amount of adsorption was about 38.9 mg g(-1) under the adsorbent dose of 5 g L-1, 500 mg L-1 CV dye concentration, and pH 6.9. The interaction between the CV molecule and the PAA@TiO2 nanocomposite surface was studied using Monte Carlo (MC) and molecular dynamics (MD) simulations. The negative value of the Eads (- 586.56 kcal mol(-1)) of the CV molecules onto the PAA@TiO2 nanocomposite surface gives credibility to the experimental results. All obtained results showed that PAA@TiO2 hybrid polymer nanocomposite could be an alternative adsorbent for crystal violet dye removal from wastewater.Article Citation - WoS: 29Citation - Scopus: 34Preparation and Characterization of a Novel Diatomite-Based Composite and Investigation of Its Adsorption Properties for Uranyl Ions(Springer, 2019-07-20) Senol, Zeynep Mine; Arslan, Dilek Senol; Simsek, Selcuk; Şenol Arslan, DilekIn this research, Polyacrylamide-diatomite (PAA-D) composite was used as adsorbent for the efficient removal of uranyl ions from aqueous solution. The chemical and morphological properties of PAA-D composite were confirmed by several analysis. Batch experiments were performed as a function of solution pH, initial concentration, kinetic, thermodynamic and recovery. The maximum metal uptake capacity was found as 0.085 mol kg(-1). Kinetic data were best interpreted by a pseudo second order model. Thermodynamic findings showed that the adsorption process was exothermic, spontaneous and process with increased disorderliness at solid/solution interface. The recovery studies showed that PAA-D composite had good adsorption/desorption performance.Article Citation - WoS: 2Citation - Scopus: 2Diffuse-Layer Surface Potentials of Colemanites Mined in Turkey(Oficyna Wydawnicza Politechniki Wrocławskiej, 2022-07-07) Arslan, Dilek Senol; Drelich, Jaroslaw W.; Senol-Arslan, DilekColemanite crystal specimens were handpicked at Kestelek, Emet (Hisarcik, Espey), Bigadic mines in Turkey for characterization of their composition and surface potential. X-ray diffraction analysis revealed no differences in mineralogical makeup of the crystals, but elemental analysis indicated differences in the type of trace (<0.1 wt%) elements. Zeta potential measurements showed small differences in zeta potential values, with isoelectric points (iep) varying from about pH = 9.6 to pH = 10.2. However, no correlation was found between iep and the type of trace elements. Additionally, atomic force microscopy (AFM) was employed to measure the colloidal interactions between a silicon nitride (Si3N4) cantilever tip and colemanite crystal surfaces in 1 wt% colemanite-saturated aqueous solutions at three different pHs (8.4, 9.4 and 11). The Derjaguin-Landau-Verwey-Overbeek theory (DLVO) was applied to examine the AFM tip interactions with colemanite surfaces in an aqueous solution of colemanite saturated solutions. The results revealed attractive forces at pH = 8.4 and 9.4 and repulsive forces at pH = 11, confirming the location of an isoelectric point for colemanite specimens somewhere between pH = 9.5 and pH = 10.1. Theoretical analysis of the force curves using the DLVO theory allowed for assessment of both surface charge density and surface potential for colemanite specimens used in this study.
