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Browsing by Author "Ari, Betul"

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    Boric Acid Versus Boron Trioxide as Catalysts for Green Energy Source H2 Production From Sodium Borohydride Methanolysis
    (2021) Demirci, Sahin; Ari, Betul; Sengel, Sultan B.; Inger, Erk; Sahiner, Nurettin
    Here, boric acid (H3BO3) and its dewatered form, boron trioxide (B2O3) were tested as catalysts for hydrogen (H2) evolution in the methanolysis of sodium borohydride (NaBH4) in methanol. Parameters such as catalyst types and their amounts, NaBH4 concentration, and the reaction temperature affecting the hydrogen generation rate (HGR) were studied. It has been found that H3BO3 and B2O3 catalyzed methanolysis reaction of NaBH4 follow up first-order kinetics relative to the concentration of NaBH4. Furthermore, the conversion and activity of these catalysts were examined to determine their performance in ten consecutive use. Interestingly, H3BO3 and B2O3 have demonstrated superior catalytic performances in methanolysis of NaBH4 comparing to the studies published in literature with the activation energy of respectively 22.08 kJ.mol-1, and 23.30 kJ.mol-1 in H2 production. The HGR was calculated as 6481 mL.min-1.g-1 and 5163 mL.min-1.g-1 for H3BO3 and B2O3 catalyst, respectively for 50 mg catalyst at 298 K. These results are comparably better than most metal nanoparticle catalysts used for H2 production in addition to the naturally occurring boron-based environmentally friendliness of these materials.
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    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.
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