Browsing by Author "Sunol, Aydin K."

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Citation - WoS: 27
Citation - Scopus: 29
Catalytic activity of metal-free amine-modified dextran microgels in hydrogen release through methanolysis of NaBH₄
(Wiley, 2020) Inger, Erk; Sunol, Aydin K.; Sahiner, Nurettin
Polymeric microgels were prepared from dextran (Dex) by crosslinking linear natural polymer dextran with divinyl sulfone (DVS) with a surfactant-free emulsion technique resulting in high gravimetric yield of 78.5 +/- 5.3% with wide size distribution. Dex microgels were chemically modified, and then used as catalyst in the methanolysis of NaBH4 to produce H-2. The chemical modification of Dex microgel was done on epichlorohydrin (ECH)-reacted Dex microgels with ethylenediamine (EDA), diethylenetriamine (DETA), and triethylenetetraamine (TETA) in dimethylformamide (DMF) at 90 degrees C for 12 hours. The modified dextran-TETA microgels were protonated using treatment with hydrochloric acid (HCl) and m-Dex microgels-TETA-HCl was found to be a very efficient catalyst for methanolysis of NaBH4 to produce H-2. The effects of reaction temperature and NaBH4 concentration on H-2 generation rates were investigated and m-Dex microgels-TETA-HCl catalyst possessed excellent catalytic performances with 100% conversion and 80% activity at end of 10 consecutive uses and was highly re-generatable with simple HCl treatment. Interestingly, m-Dex microgels-TETA-HCl catalyst can catalyze NaBH4 methanolysis reaction in a mild temperature range 0 to 35 degrees C with Ea value of 30.72 kJ/mol and in subzero temperature range, -20 to 0 degrees C with Ea value of 32.87 kJ/mol, which is comparable with many catalysts reported in the literature.
Citation - WoS: 6
Citation - Scopus: 6
Optimized Porous Carbon Particles From Sucrose and Their Polyethyleneimine Modifications for Enhanced Co₂ Capture
(Mdpi, 2024) Ari, Betul; Inger, Erk; Sunol, Aydin K.; Sahiner, Nurettin
Carbon dioxide (CO2), one of the primary greenhouse gases, plays a key role in global warming and is one of the culprits in the climate change crisis. Therefore, the use of appropriate CO2 capture and storage technologies is of significant importance for the future of planet Earth due to atmospheric, climate, and environmental concerns. A cleaner and more sustainable approach to CO2 capture and storage using porous materials, membranes, and amine-based sorbents could offer excellent possibilities. Here, sucrose-derived porous carbon particles (PCPs) were synthesized as adsorbents for CO2 capture. Next, these PCPs were modified with branched- and linear-polyethyleneimine (B-PEI and L-PEI) as B-PEI-PCP and L-PEI-PCP, respectively. These PCPs and their PEI-modified forms were then used to prepare metal nanoparticles such as Co, Cu, and Ni in situ as M@PCP and M@L/B-PEI-PCP (M: Ni, Co, and Cu). The presence of PEI on the PCP surface enables new amine functional groups, known for high CO2 capture ability. The presence of metal nanoparticles in the structure may be used as a catalyst to convert the captured CO2 into useful products, e.g., fuels or other chemical compounds, at high temperatures. It was found that B-PEI-PCP has a larger surface area and higher CO2 capture capacity with a surface area of 32.84 m(2)/g and a CO2 capture capacity of 1.05 mmol CO2/g adsorbent compared to L-PEI-PCP. Amongst metal-nanoparticle-embedded PEI-PCPs (M@PEI-PCPs, M: Ni, Co, Cu), Ni@L-PEI-PCP was found to have higher CO2 capture capacity, 0.81 mmol CO2/g adsorbent, and a surface area of 225 m(2)/g. These data are significant as they will steer future studies for the conversion of captured CO2 into useful fuels/chemicals.
Citation - WoS: 15
Citation - Scopus: 16
Pei Modifiednatural Sands of Florida as Catalysts for Hydrogen Production From Sodium Borohydride Dehydrogenation in Methanol
(Wiley-hindawi, 2021) Inger, Erk; Demirci, Sahin; Can, Mehmet; Sunol, Aydin K.; Philippidis, George; Sahiner, Nurettin
Sand samples from Tampa (T) and Panama (P) City beaches in Florida were used as catalysts for dehydrogenation of NaBH4 in methanol. T and P sand samples were sieved to <250, 250 to 500, and >500 mu m sizes, and the smallest fractions resulted in faster hydrogen generation rates (HGR), 565 +/- 18 and 482 +/- 24 mL H-2 (min.g of catalyst)(-1), respectively. After various base/acid treatments, HGR values of 705 +/- 51 and 690 +/- 47 mL H-2 (min g of catalyst)(-1) for HCl-treated T and P sand samples were attained, respectively. Next, T and P sand samples were modified with polyethyleneimine (PEI) that doubled the HGR values, 1344 +/- 103, and 1190 +/- 87 mL H-2 (min.g of catalyst)(-1) and increased similar to 8-fold, 4408 +/- 187, and 3879 +/- 169 mL H-2 (min g of catalyst)(-1), correspondingly after protonation (PEI+). The Ea values of T and P sand samples were calculated as 24.6 and 25.9 kJ/mol, and increased to 36.1, and 36.6 kJ/mol for T-PEI(+)and P-PEI(+)samples, respectively.