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  • MakaleYalnız künye2026Scopus SJRQ2
    Comparative Analysis of Sequential Electrooxidation and Electrocoagulation Processes for Leachate Treatment

    Ogedey, Aysenur; Oguz, Ensar

    This study aims to improve the removal efficiency of chemical oxygen demand (COD), NH₃-N, and turbidity from Bingöl leachate through a sequential electrochemical process. This process includes electrooxidation (EO) with Ti/PdO-CoO anodes and stainless-steel cathodes, followed by electrocoagulation (EC) with aluminum anodes and stainless-steel cathodes. The sequential electrochemical process lasted 400 min, consisting of 360 min of EO followed by 40 min of EC process. At pH 5, COD and turbidity reached optimal removal efficiencies of 89% and 99.9%, respectively, while NH₃-N achieved 88.5% at pH 9.5. These results indicate that the sequential electrochemical process was most effective under these pH values for removing organic matter, nitrogen, and suspended solids. The sequential electrochemical process led to significant improvements in the removal efficiencies of COD, NH₃-N, and turbidity, with increases of 32.5%, 44%, and 6.9%, respectively, compared to the EO process. The sequential electrochemical process showed improvements of 9.5% in COD and NH₃-N removal, and 1.2% in turbidity removal, compared to the results of the EC process. The pseudo-first-order (PFO) reaction rates for the EO and EC processes were determined, resulting in high R2 values (0.98–0.99). Additionally, the total consumption cost of the EO process was higher than that of the EC process. After the sequential electrochemical process, the consumption cost increased from $13.586/kg COD to $24.332/kg COD as the current density increased from 15 mA/cm2 to 25 mA/cm2.

    • SDG 6 · Temiz Su ve Sanitasyon
    • SDG 12 · Sorumlu Üretim ve Tüketim
    AtıfScopus1WoS1OpenAlex1
    ScopusWeb of Scienceİncele
  • MakaleAçık Erişim2026Scopus SJRQ2
    Green Chemistry Meets Advanced Materials: Synthesis and Adsorption Performance of Ti3CNTx MXenes for Basic Red 46 Dye Removal

    Aydın, Ekrem; Çelik, Aytekin; Köse, Yusuf; Hasar, Halil

    In this study, Ti₃CNTₓ MXene nanosheets were synthesized from Ti₃AlCNTₓ MAX phase via two selective Al-etching routes: (i) direct hydrofluoric acid (HF) treatment and (ii) in-situ HF generation using a LiF + HCl mixture. Both approaches were systematically compared to evaluate their effects on structural integrity, surface chemistry, and adsorption performance toward the cationic dye Basic Red 46 (BR 46). Comprehensive physicochemical characterizations—including SEM–EDX, XRD, XPS, Raman spectroscopy, AFM, contact angle analysis, and TGA—confirmed successful Al removal and MXene formation for both methods, with notable differences in surface terminations and layer morphology. Batch adsorption experiments were conducted across a wide range of pH values (2–11), temperatures (25–60 °C), contact times (0–90 min), adsorbent dosages (0.05–0.40 g), and initial dye concentrations (10–50 mg/L). The HF-etched Ti₃CNTₓ exhibited rapid adsorption, achieving 99.6% removal at pH 2 within 20 min, whereas the LiF + HCl-etched sample demonstrated superior performance at moderate-to-alkaline pH and maintained high efficiency at lower dosages. Langmuir isotherm fitting revealed maximum adsorption capacities of 19.24 mg/g (HF route) and 28.01 mg/g (LiF + HCl route), supporting monolayer adsorption on homogeneous sites. Temperature-dependent studies further indicated an endothermic and spontaneous adsorption mechanism. Overall, the LiF + HCl route offers a greener and safer alternative to conventional HF etching while delivering competitive adsorption performance, improved structural stability, and faster equilibrium. These findings highlight the potential of sustainably synthesized Ti₃CNTₓ MXenes as high-performance adsorbents for dye-laden industrial wastewater treatment.

    • SDG 6 · Temiz Su ve Sanitasyon
    • SDG 12 · Sorumlu Üretim ve Tüketim
    AtıfScopus2WoS2OpenAlex1
    ScopusWeb of Scienceİncele
  • MakaleAçık Erişim2021Scopus SJRQ2
    Comparative Toxicity of Alpha and Gamma Iron Oxide Nanoparticles in Rainbow Trout: Histopathology, Hematology, Accumulation, and Oxidative Stress

    Gürkan, Mert; Gürkan, Selin Ertürk; Yılmaz, Sevdan; Ateş, Mehmet

    In this study, alpha and gamma iron oxide nanoparticles, characterizations, toxic effects after being exposed to rainbow trout (Oncorhynchus mykiss) at 0, 1, 10 and 25 mg/L concentrations for 10 days, and then 10-day recovery period without any nanoparticle exposure were examined for histopathological (kidney, liver and gill), hematological, iron accumulation and potential for oxidative stress (TBARS and GSH). Histopathological damages significant at the exposure of increasing concentrations of both nanoparticles (increase in melanomacrophage aggregations, epithelial tissue deformations, cytoplasmic vacuolizations, fatty changes, necrosis, pyknosis, hyperplasia, hypertrophy, lamellar fusions, capillary dilatations). Gamma nanoparticles were determined to accumulate more than the alpha nanoparticles. The most Fe accumulation was detected in the liver. The findings of oxidative stress parameters showed that both nanoparticles have the potential to generate oxidative stress. It was concluded that the exposure of alpha and gamma nanoparticles at specified concentrations and durations had a toxic effect on rainbow trout and the toxicity of these nanoparticles was similar.

    • SDG 3 · Sağlık ve Kaliteli Yaşam
    AtıfScopus18WoS12OpenAlex16
    ScopusWeb of Scienceİncele
  • MakaleYalnız künye2018Scopus SJRQ2
    Microbial Sorption of Uranium Using Amycolatopsis sp. K47 Isolated from Uranium Deposits

    Celik, Fatih; Camas, Mustafa; Kyeremeh, Kwaku; Sazak Camas, Anil

    The increasing contamination of soils, sediments, and water with heavy metals through natural and industrial processes is a worldwide problem. Mining processes produce tons of material contaminated with radionuclides such as U and different heavy metals such as Cd, Ni, and Pb. U(VI) adsorbs strongly on bacteria, exhibiting pH-dependent adsorption behavior that is caused by a range of uranyl surface complexes on bacteria cell walls. The Amycolatopsis sp. K47 was isolated from Manisa Koprubasi Kasar open-cast uranium mine and identified for the first time. Using the batch adsorption method, the biosorption potential of this microbe was investigated by studying the effects of changes in pH (1–10), biomass dose (0.1–5 g/l), initial uranium metal concentration (5–200 mg/l), contact time (5–180 min), and temperature (20–60 °C). Interpretation of FTIR data obtained for both the uranium loaded and unloaded Amycolatopsis sp. K47 biomass showed the presence of carboxylic acid, hydroxyl, and amide functional groups that could interact with uranium ions. Scanning electron microscopy images demonstrated that uranium was intensely adsorbed on the microbial biomass surface. The sorption isotherms were investigated by analysis of the Langmuir, Freundlich, and Dubinin–Radushkevich (D–R) models. The Langmuir isotherm model was found to show the best fit for the experimental data obtained. Furthermore, thermodynamic parameters, such as ΔH°, ΔS°, and ΔG°, were calculated using adsorption equilibrium constant obtained from the Langmuir isotherm. The optimal experimental conditions were determined to be pH = 4, C0 = 40 ppm, t = 150 min, temp. = 40 °C, and abs. dose = 1 g/l, and the corresponding U(VI) removal efficiency was about 97 ± 2%.

    • SDG 6 · Temiz Su ve Sanitasyon
    AtıfScopus16WoS14OpenAlex15
    ScopusWeb of Scienceİncele
  • MakaleAçık Erişim2016Scopus SJRQ2
    Toxicity of Engineered Nickel Oxide and Cobalt Oxide Nanoparticles to Artemia salina in Seawater

    Ates, Mehmet; Demir, Veysel; Arslan, Zikri; Camas, Mustafa; Celik, Fatih

    In this study, the effects of exposure to engineered nickel oxide (NiO 40-60 nm) and cobalt oxide (CoO < 100 nm) nanoparticles (NP) were investigated on Artemia salina. Aggregation and stability of the aqueous NP suspensions were characterized by DLS and TEM. Acute exposure was conducted on nauplii (larvae) in seawater in a concentration range from 0.2 to 50 mg/L NPs for 24 h (short term) and 96 h (long term). The hydrodynamic diameters of NiO and CoO NPs in exposure medium were larger than those estimated by TEM. Accumulation rate of NiO NPs were found to be four times higher than that of CoO NPs under the same experimental conditions. Examinations under phase contrast microscope showed that the nanoparticles accumulated in the intestine of Artemia, which increased with increasing exposure concentration. Differences were observed in the extent of dissolution of the NPs in the seawater. The CoO NPs dissolved significantly while NiO NPs were relatively more stable. Oxidative stress induced by the NP suspensions was measured by malondialdehyde assay. Suspensions of NiO NPs caused higher oxidative stress on nauplii than those of CoO NPs. The results imply that CoO and NiO NPs exhibit toxicity on Artemia (e. g., zooplankton) that is an important source of food in aquatic food chain.

    • SDG 6 · Temiz Su ve Sanitasyon
    • SDG 14 · Sudaki Yaşam
    AtıfWoS59OpenAlex71
    Web of Scienceİncele
  • MakaleYalnız künye2015Scopus SJRQ2
    Removal of Phosphate from Aqueous Solutions by Chemical- and Thermal-Modified Bentonite Clay

    Tanyol, Mehtap; Yonten, Vahap; Demir, Veysel

    The study investigated phosphate adsorption from aqueous solutions using chemical- and thermal-modified bentonite in batch system. The adsorbent was characterized by SEM, BET, and FTIR spectroscopy. Contact time, beginning phosphate concentration, pH of the solution, and the effects of the temperature on phosphate adsorption capacity were determined by a series of experimental studies. In a wide pH range (3-10), high phosphate removal yields were obtained (between 94.23 and 92.26 %), and with the increase in temperature (from 25 to 45 degrees C), phosphate removal increased. Langmuir and Freundlich isotherms were used to determine the sorption equilibrium, and the results demonstrated that equilibriumdata displayed better adjustment to Langmuir isotherm than the Freundlich isotherm. Phosphate sorption capacity, calculated using Langmuir equation, is 20.37 mg g(-1) at 45 degrees C temperature and pH 3. Mass transfer and kinetic models were applied to empirical findings to determine the mechanism of adsorption and the potential steps that control the reaction rate. Both external mass transfer and intra-particle diffusion played a significant role on the adsorption mechanism of phosphate, and adsorption kinetics followed the pseudo-second-order-type kinetic. Furthermore, thermodynamic parameters (Delta H degrees, Delta G degrees, Delta S degrees) which reveal that phosphate adsorption occur spontaneously and in endothermic nature were determined. The results of this study support that bentonite, which is found abundant in nature and modified as an inexpensive and effective adsorbent, could be used for phosphate removal from aqueous solutions.

    • SDG 6 · Temiz Su ve Sanitasyon
    • SDG 12 · Sorumlu Üretim ve Tüketim
    AtıfWoS26OpenAlex27
    Web of Scienceİncele
Tam Kayıt
AlanDeğerDil
creativeworkseries.issn0049-6979
dc.date.accessioned2026-10-28T14:53:48.192016018Z
dc.date.available2026-10-28T14:53:48.192016018Z
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/984
dc.publisherSpringer Nature
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleWater, Air, and Soil Pollution