WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7150
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Article Citation - WoS: 6Citation - Scopus: 6A New Electro-Biomembrane Integrated Renewable-Based System To Produce Power, Fresh Water and Hydrogen for Sustainable Communities(Elsevier, 2025) Goren, A. Yagmur; Dincer, Ibrahim; Khalvati, AliAs the consequences of global warming become more severe, it is more crucial than ever to capitalize on all locally accessible potential renewable energy sources and produce sufficient useable energy outputs to meet community demands while causing the least damage to the ecosystem. Therefore, this paper focuses on a unique parabolic trough collector solar system-powered electro-biomembrane unit that combines a heat and power system with fresh water, electricity and hydrogen production. The proposed integrated system contains the following subsystems: a combining parabolic trough collector solar system, an organic Rankine cycle, a steam Rankine cycle, a multi-stage flash desalination system, and an electro-biomembrane H2 and freshwater production system. A thorough analysis and parametric research are performed on the multigeneration system to determine how important characteristics affect system performance and evaluate the energy and exergy efficiencies, and exergy destruction levels for particular system elements. The study results show that solar irradiation is the most critical parameter for improving system performance. The highest freshwater production of 1,303,333.3 L/day is observed at the solar irradiation of 935,768 kWh/day. Furthermore, the combined output of three electricity production technologies exceeds 2,000,000 kWh/day, highlighting the ability of the system to harness solar thermal energy effectively. The study findings indicate that using solar power and biomass as renewable energy sources, the proposed integrated system provided 328.56 kg of biohydrogen per day. Overall, the energy and exergy efficiencies of the integrated system are obtained as 34.3 and 29.5 %, respectively.Article Citation - WoS: 14Citation - Scopus: 17Cleaner Production of Biohydrogen Using Poplar Leaves: Experimental and Optimization Studies(Elsevier Sci Ltd, 2024) Goren, A. Yagmur; Kenez, Muratcan; Dincer, Ibrahim; Khalvati, AliBiohydrogen (bioH2) is recognized as a potential carbon-neutral energy vector, and developing novel methods has received increasing attention with a prime goal of producing H2 more efficient and cost effective manner. This study aimed to develop a unique reactor to investigate dark fermentative H2 production from poplar biomass using commercially available and inexpensive microorganism cultures. Therefore, six factors of the Box-Behnken design (BBD) were performed to evaluate the individual and combined effects of operational param-eters: acid concentration (2-10%), biomass concentration (2-10 g), initial pH (5-8), temperature (30-40 degrees C), mixing ratio (150-350 rpm), and microorganism concentration (2-6 g) on bioH2 production. Among the oper-ational parameters, the acid concentration was the most effective parameter on bioH2 production. The bioH2 production increased from 11.33 to 18.15 mg/g biomass with increasing acid concentration from 6 to 10%. Moreover, the optimum levels of operational variables were as follows: acid concentration of 9.9%, biomass amount of 2 g, pH of 6.56, temperature of 35 degrees C, mixing ratio of 345 rpm, and microorganism amount of 4.5 g for the highest bioH2 production of 20 mg/g-biomass according to the experimental design. Consequently, the bioH2 production performance of the dark fermentation process showed that bioH2 production from poplar biomass using commercially available microorganisms had a competitive advantage.Article Citation - WoS: 4Citation - Scopus: 5Breakthrough Curve Analysis of Phosphorylated Hazelnut Shell Waste in Column Operation for Continuous Harvesting of Lithium From Water(Elsevier, 2024) Recepoğlu, Yaşar Kemal; Arar, Ozguer; Yuksel, AsliIn batch-scale operations, biosorption employing phosphorylated hazelnut shell waste (FHS) revealed excellent lithium removal and recovery efficiency. Scaling up and implementing packed bed column systems necessitates further design and performance optimization. Lithium biosorption via FHS was investigated utilizing a continuous-flow packed-bed column operated under various flow rates and bed heights to remove Li to ultra-low levels and recover it. The Li biosorption capacity of the FHS column was unaffected by the bed height, however, when the flow rate was increased, the capacity of the FHS column decreased. The breakthrough time, exhaustion time, and uptake capacity of the column bed increased with increasing column bed height, whereas they decreased with increasing influent flow rate. At flow rates of 0.25, 0.5, and 1.0 mL/min, bed volumes (BVs, mL solution/mL biosorbent) at the breakthrough point were found to be 477, 369, and 347, respectively, with the required BVs for total saturation point of 941, 911, and 829, while the total capacity was calculated as 22.29, 20.07, and 17.69 mg Li/g sorbent. In the 1.0, 1.5, and 2.0 cm height columns filled with FHS, the breakthrough times were 282, 366, and 433 min, respectively, whereas the periods required for saturation were 781, 897, and 1033 min. The three conventional breakthrough models of the Thomas, Yoon-Nelson, and Modified Dose-Response (MDR) were used to properly estimate the whole breakthrough behavior of the FHS column and the characteristic model parameters. Li's extremely favorable separation utilizing FHS was evidenced by the steep S-shape of the breakthrough curves for both parameters flow rate and bed height. The reusability of FHS was demonstrated by operating the packed bed column in multi-cycle mode, with no appreciable loss in column performance.Article Selective Catalytic Hydrogenation of Cellulose Into Sorbitol With Ru-Based Catalysts(Tubitak Scientific & Technological Research Council Turkey, 2022) Orak, Ceren; Sapmaz, Aycan; Yüksel Özsen, AslıSorbitol is one of the platform chemicals and can be produced from various renewable and sustainable sources via different processes. Hydrothermal liquefaction is an effective and promising approach to produce sorbitol, since the subcritical reaction media and appropriate catalysts provide a selective production of platform chemicals. In this study, sorbitol was produced from different renewable sources (cellulose and glucose) in the presence of Ru-based catalysts (Ru/SiO2, Ru/AC, Ru/SBA-15, and Ru/SBA-15-SO3) under subcritical conditions. The highest cellulose conversion was achieved as 90% in the presence of Ru/SBA-15-SO3 for 1 h of reaction duration. The highest sorbitol yield (%) by hydrothermal liquefaction of cellulose was obtained as 6.2% by using Ru/AC for 1 h of reaction duration. A total of 99.9% of glucose conversion was achieved in the presence of all catalysts. The highest sorbitol yield (%) by hydrothermal liquefaction of glucose was found as 3.8% for 1 h of reaction duration. Owing to the results of GC-MS analysis, the intermediate products were identified, and, thus, a reaction pathway was proposed.Article Citation - WoS: 2Citation - Scopus: 1Dynamics of Co2 Consumption, and Biomass and Lipid Carbon Production During Photobioreactor Cultivation of the Diatom Cyclotella(TÜBİTAK - Türkiye Bilimsel ve Teknolojik Araştırma Kurumu, 2023) Ökten, HaticeUnderstanding of CO2 delivery and consumption dynamics in algal photobioreactors are critical to unravel microalgae’s full potential for bioproduct generation and carbon capture from flue gas streams. This study aims to expand our current understanding by cultivating the diatom Cyclotella under controlled process conditions of a bubble column photobioreactor and analyzing CO2 consumption dynamics in real time using results from an online CO2 sensor connected to the reactor exhaust. Two sets of experiments were conducted: they served to contrast the influence of silicon and nitrate (Si&N colimitation) and Si limitation, and the light availability, respectively. CO2 consumption was calculated based on the mass balance around the reactor inlet and outlet gas streams. Biomass samples and lipid extracts were analyzed for carbon (C) content to determine biomass-C and lipid-C concentrations. The outlet CO2 concentrations varied significantly with cultivation time and process conditions. More than 15% to 65% of the CO2 introduced left the reactor in the exhaust at any instance based on the set CO2 transfer rates. The highest average daily capturing efficiency was 60%. Nutrient limitation regimes imposed generated unique CO2 consumption profiles undiscernible by the biomass-C analysis, i.e. unlike Si limitation, N limitation had more immediate detrimental effects on C consumption. Final biomass-C concentration increased with increasing N and light availability, 275 mg/L vs. 336 mg/L, and 270 mg/L vs. 501 mg/L, respectively. Biomass-C based capturing efficiency approximations resulted in 20% to 40% underestimation. Under Si-limited conditions, the higher light intensity increased the final lipid-C to biomass-C ratio by two times (from 20% to 40%) and the final lipid-C concentration and peak productivity by four times (from 56 mg/L to 216 mg/L, from 7 to 30 mg/L-day, respectively). This study demonstrates online exhaust CO2 concentration-based analysis’s unique capabilities for assessing carbon availability and capture, organic-C production, and its diversion to biomass and lipid production.Article Citation - WoS: 13Citation - Scopus: 14Perspectives of Biomass Catalytic Fast Pyrolysis for Co-Refining: Review and Correlation of Literature Data From Continuously Operated Setups(American Chemical Society, 2022) Prins, Wolter; Yıldız, GürayFor the co-processing of pyrolysis-based biocrudes within petroleum refineries, a degree of conditioning/upgrading involving the cracking of the oligomers and (partial) removal of oxygen could be operationally beneficial. By inducing a complex set of reactions in biomass-derived fast pyrolysis vapors, catalytic fast pyrolysis (CFP) ensures significant changes in oxygen functionalities and alleviates oxygen concentration in the resulting liquid intermediate (CFP-oil). Due to its reduced oxygen content and acidity, CFP-oil could be considered suitable for co-feeding in FCC units and/or for co-hydrotreatment (co-HT) with gas oils within the existing crude oil processing infrastructure. On the operational side, however, research concerning CFP of biomass has shown poor results: deoxygenation of pyrolysis vapors goes along with a progressive reduction in CFP-oil yield. Apart from any control over catalyst activity, selectivity, and lifetime, the other critical issue is in the process design, which is complicated by rapid catalyst deactivation through coke formation and catalyst poisoning by biomass-originated minerals. This review analyzes the outcome of research efforts concerning in- and ex situ CFP of biomass based on carefully selected literature studies reporting the results obtained from meso- and macrolevel laboratory-scale setups, pilot, process development units (PDU), and (semi-) commercial process units, wherein the biomass feedstock and catalyst is fed continuously. Key operational aspects such as the reactor technology, reactive medium, processing mode, and optimization of process parameters are addressed. The performances of continuously operated CFP units were benchmarked through a comparison of yields and elemental compositions of (by-)products. Despite the considerable research efforts related to CFP technology development, the co-processing of CFP-oil is still in its infancy. However, in close collaboration with refinery professionals, it could be made a serious candidate for biobased co-feeding. For refinery integration, quality parameters of CFP-oil, e.g., acidity, stability, and miscibility, should be considered as crucial as its oxygen content.Article Citation - WoS: 2Citation - Scopus: 2Evaluating the Performance of Conventional Daf and Posidaf Processes for Cyanobacteria Separation at a Pilot Plant Scale(IWA Publishing, 2022) Yap, Russell K.L.; Rao, N. R.H.; Holmes, M.; Whittaker, Michael; Stuetz, Richard M.; Jefferson, Bruce; Bulmuş, Volga; Peirson, William Leslie; Henderson, R. K.In this work, a commercially available water treatment polymer poly(N,N-diallyl-N,N-dimethylammonium chloride) (PDADMAC) and a hydrophobically modified polymer (HMP) designed to adhere to bubble surfaces were applied for the first time in the novel Posi-dissolved air flotation process (PosiDAF) that uses polymer-modified bubbles, at pilot-scale for the treatment of waste stabilisation pond samples rich in algae. It was found that PDADMAC in PosiDAF gave comparable removal to that achieved using conventional DAF at .95% cell separation. Furthermore, the float layer was more uniform and thicker with up to 8% solid contents compared to conventional DAF, which comprised discrete floc clusters with an average solid concentration of ∼4.1%. In contrast to the use of PDADMAC, the application of the HMP did not achieve similarly good separation at pilot scale. It was hypothesised that this may be due to the micellisation of the HMP on the bubble surface, creating unstable bubbles that coalesced and prevented polymer-bubble-cell interactions, which are crucial for effective cell separation. On comparison of the costs of PosiDAF and conventional DAF, it was found that PosiDAF resulted in cost-savings of up to 74% due to low chemical consumption. In summary, PosiDAF reduced chemical cost and increased solid contents in the metal-free float.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: 11Citation - Scopus: 12Novel Hybrid Process for the Conversion of Microcrystalline Cellulose To Value-Added Chemicals: Part 1: Process Optimization(Springer Verlag, 2016) Akın, Okan; Yüksel, AslıIn this paper, a novel hybrid process for the treatment of microcrystalline cellulose (MCC) under hot-compressed water was investigated by applying constant direct current on the reaction medium. Constant current range from 1A to 2A was applied through a cylindrical anode made of titanium to the reactor wall. Reactions were conducted using a specially designed batch reactor (450 mL) made of SUS 316 stainless steel for 30–120 min of reaction time at temperature range of 170–230 °C. As a proton donor H2SO4 was used at concentrations of 1–50 mM. Main hydrolysis products of MCC degradation in HCW were detected as glucose, fructose, levulinic acid, 5-HMF, and furfural. For the quantification of these products, High Performance Liquid Chromatography (HPLC) and Gas Chromatography with Mass Spectroscopy (GC–MS) were used. A ½ fractional factorial design with 2-level of four factors; reaction time, temperature, H2SO4 concentration and applied current with 3 center points were built and responses were statistically analyzed. Response surface methodology was used for process optimization and it was found that introduction of 1A current at 200 °C to the reaction medium increased Total Organic Carbon (TOC) and cellulose conversions to 62 and 81 %, respectively. Moreover, application of current diminished the necessary reaction temperature and time to obtain high TOC and cellulose conversion values and hence decreased the energy required for cellulose hydrolysis to value added chemicals. Applied current had diverse effect on levulinic acid concentration (29.9 %) in the liquid product (230 °C, 120 min., 2 A, 50 mM H2SO4). © 2016, Springer Science+Business Media Dordrecht.