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Catalytic performance of bimetallic Ni-Pt nanoparticles supported on activated carbon, gamma-alumina, zirconia, and ceria for hydrogen production in sulfur-iodine thermochemical cycle

机译:活性炭,γ-氧化铝,氧化锆和二氧化铈负载的双金属Ni-Pt纳米颗粒在硫碘热化学循环中的产氢催化性能

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摘要

Bimetallic Ni-Pt nanoparticles supported on four different supports (activated carbon (AC)), γ-alumina, zirconia, and ceria) were prepared by modified impregnation-reduction technique for decomposition of hydrogen iodide to hydrogen and iodine, in the thermochemical water-splitting sulfur-iodine (SI) cycle. The catalysts were characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), and Brunauer–Emmett–Teller (BET) method to find their structure, morphology, and surface area, respectively. High metal dispersions (Ni-Pt) were obtained with particle sizes of the order of 10 nm or lesser, in the high-surface-area supports. The hydrogen iodide-decomposition results showed catalytic activity of Ni-Pt nanoparticles in the following order on different supports: Ni(2.5%)-Pt(2.5%)/AC > Ni(2.5%)-Pt(2.5%)/γ-alumina > Ni(2.5%)-Pt(2.5%)/Zirconia > Ni(2.5%)-Pt(2.5%)/Ceria. Bimetallic Ni(2.5%)-Pt(2.5%)/AC also showed excellent stability for 100 h in the hydrogen iodide-decomposition reaction, and with a higher performance relative to the corresponding Pt supported catalyst under the same operating conditions.
机译:通过改进的浸渍-还原技术,在热化学水中将碘化氢分解为氢和碘,制备了负载在四种不同载体(活性炭(AC),γ-氧化铝,氧化锆和二氧化铈)上的双金属Ni-Pt纳米粒子。分裂硫-碘(SI)循环。通过粉末X射线衍射(XRD),透射电子显微镜(TEM)和Brunauer-Emmett-Teller(BET)方法对催化剂进行了表征,以分别找到其结构,形态和表面积。在高表面积载体中获得具有约10nm或更小的粒度的高金属分散体(Ni-Pt)。碘化氢的分解结果表明,Ni-Pt纳米粒子在不同载体上的催化活性依次为:Ni(2.5%)-Pt(2.5%)/ AC> Ni(2.5%)-Pt(2.5%)/γ-氧化铝> Ni(2.5%)-Pt(2.5%)/氧化锆> Ni(2.5%)-Pt(2.5%)/二氧化铈。 Ni(2.5%)-Pt(2.5%)/ AC双金属在碘化氢分解反应中100小时也显示出出色的稳定性,并且在相同的操作条件下,相对于相应的Pt负载型催化剂,其性能更高。

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