Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Citation - WoS: 10Citation - Scopus: 11Liquefaction of Oak Wood Using Various Solvents for Bio-Oil Production(AMER CHEMICAL SOC, 2023) Öcal, Bulutcem; Yüksel, AslıRapidly increasing global energy demand resulting from the growing population and worldwide development has increased the consumption of limited fossil fuel. The usage causes severe environmental deterioration by CO2 emission, which has sparked interest in finding green, renewable, and sustainable alternative sources of energy. Bio-oil, derived from several biomasses via liquefaction, is a promising candidate to replace fossil fuels. Turkey's land (27%) is covered with forested areas (consisting of mostly oak trees). Therefore, it has great potential for cheap lignocellulosic feedstock forest residues from industrial applications and harvesting. In the present study, the thermal liquefaction of oak wood particles (OWP) was performed using various solvents in addition to water, namely, ethanol, 1-butanol, and 1,4-dioxane. The experiments were carried out in a batch reactor for 1 and 2 h residence times at different temperatures (210, 240, and 270 degrees C). Bio-oil samples obtained at 270 degrees C and a 1 h residence time determined as optimum conditions were analyzed with TGA, CHNS elemental analysis, FTIR, and GC-MS. 1,4-Dioxane showed the best performance in yielding the maximum bio-oil with 51.8% at those conditions. The higher heating values of the bio-oils ranged from 22.1 to 35 MJ/kg. Phenolic groups were the predominant components of bio-oil produced from OWP, while the intensity of alcohols, ketones, and acids varied based on used solvents. Based on energy recovery calculations, the enhancement of pristine OWP's energy efficiency depended on bio-oil yield, and quality was confirmed for all solvent types (1,4-dioxane > 1-butanol > water > ethanol).Article Citation - WoS: 10Citation - Scopus: 12Novel Hybrid Adsorption-Electrodialysis (aded) System for Removal of Boron From Geothermal Brine(American Chemical Society, 2022) Altınbaş, Bekir Fırat; Orak, Ceren; Ökten, Hatice Eser; Yüksel, AslıA novel hybrid adsorption-electrodialysis (AdED) system to remove environmentally harmful boron from geothermal brine was designed and effective operating parameters such as pH, voltage, and flow rate were studied. A cellulose-based adsorbent was synthesized from glycidyl methacrylate (GMA) grafted cellulose and modified with a boron selective n-methyl-d-glucamine (NMDG) group and characterized with SEM-EDX, FT-IR, and TGA analyses. Batch adsorption studies revealed that cellulose-based adsorbent showed a remarkable boron removal capacity (19.29 mg/g), a wide stable operating pH range (2-10), and an adsorption process that followed the Freundlich isotherm (R2= 0.95) and pseudo-second-order kinetics (R2= 0.99). In the hybrid AdED system, the optimum operating parameters for boron removal were found to be a pH of 10, a voltage of 10 V, a flow rate of 100 mL/min, and an adsorbent dosage of 4 g/L. The presence of the adsorbent in the hybrid system increased boron removal from real geothermal brine (containing 199 ppm boron) from 7.2% to 73.3%. The results indicate that the designed AdED system performs better than bare electrodialysis for boron removal from ion-rich real geothermal brine while utilizing environmentally friendly cellulose-based adsorbent.Article Citation - WoS: 11Citation - Scopus: 12Box-Behnken Design for Hydrogen Evolution From Sugar Industry Wastewater Using Solar-Driven Hybrid Catalysts(American Chemical Society, 2022) Orak, Ceren; Yüksel, AslıHydrogen is a clean and green fuel and can be produced from renewable sources via photocatalysis. Solar-driven hybrid catalysts were synthesized and characterized (scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD), photoluminescence (PL) spectroscopy, and UV-vis diffuse reflectance spectroscopy (DSR)), and the results implied that graphene-supported LaRuO3is a more promising photocatalyst to produce hydrogen and was used to produce hydrogen from sugar industry wastewater. To investigate the main and interaction effects of reaction parameters (pH, catalyst amount, and [H2O2]0) on the evolved hydrogen amount, the Box-Behnken experimental design model was used. The highest hydrogen evolution obtained was 6773 μmol/gcatfrom sugar industry wastewater at pH 3, 0.15 g/L GLRO, and 15 mM H2O2. Based on the Pareto chart for the evolved hydrogen amount using GLRO, among the main effects, the only effective parameter was the catalyst amount for the photocatalytic hydrogen evolution from sugar industry wastewater. In addition, the squares of pH and two-way interaction of pH and [H2O2]0were also statistically efficient over the evolved hydrogen amount.Article Citation - WoS: 7Citation - Scopus: 7Cross-Linked Phosphorylated Cellulose as a Potential Sorbent for Lithium Extraction From Water: Dynamic Column Studies and Modeling(American Chemical Society, 2022) Recepoğlu, Yaşar Kemal; Yüksel, AslıPhosphorylated functional cellulose was cross-linked with epichlorohydrin at different ratios because it is a very hydrophilic substance that instantly swells to form a hydrogel when it comes into contact with water. It was aimed to utilize a continuously packed bed column to recover lithium from water under varying operating conditions such as flow rate and bed height. The characterization results confirmed cross-linking based on morphology, structure, surface area, and thermal stability differences. Lithium recovery was more efficient with a low flow rate, but the dynamic sorption process was independent of bed height. The total capacities at the three flow rates with 1.5 cm bed height were 33.56, 30.15, and 25.54 mg g-1, and the total saturation times at the three different bed heights with 0.5 mL min-1 flow rate were 659, 1001, and 1007 min, respectively. Only 15.75 mL of 5% H2SO4 solution was required to desorb approximately 100% of Li from the saturated sorbent.Article Citation - WoS: 13Citation - Scopus: 12Comparison of Photocatalytic Performances of Solar-Driven Hybrid Catalysts for Hydrogen Energy Evolution From 1,8–diazabicyclo[5.4.0]undec-7 (dbu) Solution(Elsevier, 2022) Orak, Ceren; Yüksel, AslıHydrogen is evolved from 1,8–Diazabicyclo [5.4.0]undec-7-ene (DBU) model solution which is a nitrogen-containing heterocyclic organic compound using different solar-driven hybrid photocatalysts. A characterization study is performed and the results of PL analysis show that the most promising solar-driven hybrid catalyst is graphene supported LaFeO3. Then, an experimental design matrix is built using the Box Behnken model to main and interaction effects of reaction parameters (pH, catalyst loading, and [H2O2]0). Based on the experimental results relatively higher hydrogen amounts are achieved using GLFO and this finding is supported by PL analysis. The highest hydrogen amount and DBU removal are determined as 3058.31 μmol/gcat and 90.3%, respectively. Statistical analysis shows that the square of catalyst loading is the only effective parameter over the produced hydrogen amount from the DBU model solution using GLFO and the R2 of model is 92.47%. Thus, hydrogen production and wastewater treatment could be achieved via photocatalytic oxidation as concomitant.Article Citation - WoS: 21Citation - Scopus: 21Graphene-Supported Lafeo3 for Photocatalytic Hydrogen Energy Production(Wiley, 2021) Orak, Ceren; Yüksel, AslıHydrogen is a green, environmentally benign and sustainable energy source with no harmful combustion products to fulfil the increasing energy demand. Photocatalytic oxidation has various advantageous to produce hydrogen from different sources such as wastewater, alcohol solutions using different types of catalysts. Sucrose solution was chosen as a model solution to evolve hydrogen using LFO and GLFO catalysts under solar light irradiation, and graphene was used as a catalyst support to enhance the amount of produced hydrogen amount. A characterization study, which consists of SEM-EDX, BET, XRD, PL, TEM, XPS and FT-IR analyses, was carried out. A full factorial design was created via Minitab 18 to analyse the factors affecting the produced hydrogen amount, which are pH, catalyst loading, H2O2 concentration and graphene content statistically. Based on the results, graphene content is an important parameter and pH and H2O2 concentration have a synergetic effect over hydrogen production. Additionally, the effects of calcination temperature, pH, H2O2 concentration and catalyst loading over produced gases were investigated. The best promising result was obtained as 3388 mu mol/g(cat) at the following reaction conditions: 7.5 of pH, 0.1 g L-1 catalyst loading (GLFO, which is calcined at 700 degrees C) and using 15 mM H2O2 under solar light irradiation. Novelty Statement Hydrogen is produced from sucrose solution with low cost process requiring no special equipment, high pressure or temperature. First study that uses perovskite catalysts for the production of hydrogen from sucrose solution by photo-Fenton like oxidation GLFO is a promising photocatalyst for H-2 production by solar-Fenton like oxidation with the highest H-2 evaluation at 3388.34 mu mol/g(cat).Article Citation - WoS: 25Citation - Scopus: 26Phosphorylated Hazelnut Shell Waste for Sustainable Lithium Recovery Application as Biosorbent(Springer, 2021) Recepoğlu, Yaşar Kemal; Yüksel, AslıHazelnut shell waste was phosphorylated to develop a novel biosorbent based on natural renewable resource for the recovery of lithium from aqueous solution. For the synthesized biosorbent, the surface morphology and mapping by SEM-EDS, chemical properties by FTIR, elemental analysis by XPS, specific surface area by BET, crystallinity by XRD and thermal properties by TGA were elucidated elaborately. The influence of biosorbent dosage, initial concentration, temperature, contact time, pH and coexisting ions were investigated. The equilibrium sorption capacity reached 6.03 mg/g under optimal conditions (i.e., biosorbent dosage of 12.0 g/L, initial Li concentration of 100 mg/L, pH value of 5.8, sorption temperature of 25 degrees C, and sorption time of 6 min). According to the sorption behavior of the phosphorylated hazelnut shell waste the Freundlich model proved to be more suitable than the Langmuir model indicating maximum sorption capacity as 7.71 mg/g at 25 degrees C. Thermodynamic parameters obtained by different isokinetic temperatures disclosed that the ion exchange reaction was feasible, spontaneous, and exothermic where the interaction between biosorbent surface and solvent plays an important role. A preliminary test on the Li recovery from geothermal water was also performed to check its applicability in a real brine. Desorption studies at 25 degrees C revealed that relatively higher desorption efficiency and capacity were achieved at 97.4% and 5.93 mg/g, respectively with a 1.0 M H2SO4 among other regenerants (i.e., HCl and NaCl). Concentrations of Li and the other cations were determined via ICP-OES. Due to such outstanding features, the novel phosphorylated hazelnut shell waste had great potential for lithium recovery from aqueous solution by being added value as a waste and recovering a strategic element of modern life simultaneously. [GRAPHICS] .Article Citation - WoS: 31Citation - Scopus: 38Liquefaction of Waste Hazelnut Shell by Using Sub- and Supercritical Solvents as a Reaction Medium(Elsevier, 2019) Demirkaya, Emre; Dal, Orkan; Yüksel, AslıDirect thermochemical biomass degradation to obtain bio-oil by using organic solvents is not a new process type, and it has some advantages over hydrothermal liquefaction technique. However, up to our best knowledge, in this study, hazelnut shell decomposition by using ethanol, acetone and their mixtures at sub/supercritical conditions was studied for the first time in literature. Experiments were carried out between 220-300 degrees C, at three different reaction times (30, 60 and 90 min) for five different solvent ratios. Highest solid conversion achieved at 300 degrees C by using pure ethanol was 64.2%, whereas highest bio-oil yield was found as 44.2% at 300 degrees C with 50/50 (EtOH/Ac: v/v). Ethanol and acetone showed different characteristics during the reactions and their effects on the conversion and bio-oil yield were discussed. Statistical analysis showed that time, temperature, ratio and synergy between temperature-time were affecting parameters for the conversion and bio-oil yield. (C) 2019 Elsevier B.V. All rights reserved.Article Citation - WoS: 4Citation - Scopus: 4Novel Hybrid Process for the Conversion of Microcrystalline Cellulose To Value-Added Chemicals: Part 3: Detailed Reaction Pathway(Springer Verlag, 2019) Akın, Okan; Yüksel, AslıIn this study, a novel method of hydrothermal electrolysis of microcrystalline cellulose (MCC) under sub-critical water conditions (200 degrees C) was investigated by applying direct current at constant voltage with the presence of acid catalyst of 5mMH(2)SO(4). Direct current at constant voltage of 2.5V, 4.0V and 8.0V was applied between cylindrical anode (titanium) and cathode (reactor wall). Hydrothermal electrolysis reactions were carried out in a batch reactor (450mL-T316) for the reaction time of 240min. Decomposition products of MCC were analyzed by GC-MS and the decomposition pathway of cellulose under applied voltage was postulated. Levoglucosan and levoglucosenone formations were detected as the first hydrolysis products of MCC and further hydrolysis yielded to formation of glucose and fructose. The major decomposition products of cellulose were detected as levulinic acid (LA), 5-HMF and furfural. Further reactions of LA such as electrochemical decarboxylation, dehydration, hydrogenation, resulted in the formation of 2-butanone, 2-butanone-3-hydroxy, gamma-valerolactone, respectively. Most dramatic results on the product distribution were obtained at applied 2.5V voltage in which LVA and 5-HMF were selectively produced. [GRAPHICS] .Article Citation - WoS: 9Citation - Scopus: 10Novel Hybrid Process for the Conversion of Microcrystalline Cellulose To Value-Added Chemicals: Part 2: Effect of Constant Voltage on Product Selectivity(Springer Verlag, 2017) Akın, Okan; Yüksel, AslıIn this study, electrochemical degradation of microcrystalline cellulose (MCC) under hot-compressed water was investigated via application of constant voltage on reaction medium. Constant voltage ranges from 2.5 to 8.0 V was applied between anode (Titanium) and cathode (reactor wall). As an electrolyte and proton source 5–25 mM of H2SO4 was used. Reactions were carried out in a specially designed batch reactor (450 mL) made of T316 for 240 min at temperature of 200 °C.MCC decomposition products such as glucose, fructose, furfural, 5-HMF and levulinic acid were detected and quantified by High Performance Liquid Chromatography (HPLC). In the absence of electrolyte, applied voltage (2.5 and 4.0 V) decreased the total organic carbon (TOC) yield, in contrast at 8.0 V, TOC yield increased to 13%. Application of 8.0 V in hydrothermal conditions alter MCC decomposition pathway selectively to furfural (15%). Addition of electrolyte (5 mM, H2SO4) and application of 2.5 V potential increased TOC (54%) and changed the decomposition pathway in favor of 5-HMF (30%) and levulinic acid (21%). The structural changes in solid residues of electrochemically reacted MCC was analyzed by Fourier Transform Infrared Spectroscopy (FTIR) and found that MCC particles functionalized by carboxylic acid and sulfonated groups by the application of constant voltage to reaction medium. In the presence of electrolyte, under certain voltage (2.5 V), functionalization of solid particles became more obvious in FTIR spectrum results. Therefore, change in the selectivity values of degradation products were conducted with the functionalization of MCC particles due to applied voltage under sub-critical conditions.