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Production of fuel-cell grade hydrogen by sorption enhanced water gas shift reaction using Pd/Ni–Co catalysts

机译:使用Pd / Ni-Co催化剂通过吸附增强的水煤气变换反应生产燃料电池级氢气

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摘要

It has been demonstrated both thermodynamically and experimentally that fuel-cell grade hydrogen can be produced by a one-step sorption enhanced water gas shift (SEWGS) process at about 500 °C, where the water gas shift (WGS) catalyst and the CO2 sorbent are highly integrated. A synthetic CaO-based mixed oxide sorbent was also assessed, which showed a good CO2 capture capacity and stability in the cyclic operation of the SEWGS reaction. Catalysts play a significant role in CO conversion via WGS, methanation and methane steam reforming reactions. A Pd promoted Ni–Co catalyst (1%Pd/20%Ni–20%Co) derived from hydrotalcite-like material (HT) showed a high activity for WGS and methane steam reforming. The methanation activity was further reduced on 30%Ni–10%Co. There exists an optimum temperature (500 °C) for hydrogen production by the SEWGS process, where it is kinetically limited by the WGS reaction at lower temperatures (425–475 °C) and it is thermodynamically unfavorable at higher temperatures (475–550 °C). The challenges for hydrogen production by SEWGS at high CO pressures were also demonstrated, where CO pressure has shown a negative influence on WGS activity. An induction period was observed, which can be reduced by improving catalyst activity and by adding hydrogen to the reactant mixture.
机译:通过热力学和实验证明,燃料电池级氢气可通过在约500°C下通过一步吸附增强水煤气变换(SEWGS)工艺生产,其中水煤气变换(WGS)催化剂和CO2吸附剂高度集成。还评估了合成的基于CaO的混合氧化物吸附剂,该吸附剂在SEWGS反应的循环操作中显示出良好的CO2捕集能力和稳定性。催化剂在通过WGS,甲烷化和甲烷蒸汽重整反应的CO转化中起重要作用。由类水滑石(HT)衍生的Pd促进的Ni-Co催化剂(1%Pd / 20%Ni-20%Co)对WGS和甲烷蒸汽重整具有很高的活性。 30%Ni-10%Co的甲烷化活性进一步降低。存在通过SEWGS工艺制氢的最佳温度(500°C),该温度在较低温度(425–475°C)下受到WGS反应的动力学限制,而在较高温度(475–550°C)上在热力学上不利C)。还展示了SEWGS在高CO压力下生产氢气的挑战,其中CO压力已对WGS活性产生负面影响。观察到诱导期,可以通过提高催化剂活性和向反应混合物中加入氢来缩短诱导期。

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