De Maron Jacopo, Mafessanti Rodolfo, Gramazio Pio, Orfei Elisabetta, Fasolini Andrea, Basile Francesco
"Toso Montanari" Industrial Chemistry Department, Alma Mater Studiorum, Università di Bologna, 40136 Bologna, Italy.
Center for Chemical Catalysis-C3, Alma Mater Studiorum, Università di Bologna, 40136 Bologna, Italy.
Nanomaterials (Basel). 2022 Dec 22;13(1):53. doi: 10.3390/nano13010053.
Green hydrogen introduction in hard-to-abate processes is held back by the cost of substituting steam reforming plants with electrolyzers. However, green hydrogen can be integrated in properly modified reforming processes. The process proposed here involves the substitution of steam reforming with oxy-reforming, which is the coupling of the former with catalytic partial oxidation (CPO), exploiting the pure oxygen coproduced during electrolysis to feed CPO, which allows for better heat exchange thanks to its exothermic nature. With the aim of developing tailored catalysts for the oxy-reforming process, CeZrO was synthetized by microemulsion and impregnated with Rh. The Ce-based supports were calcined at different temperatures (750 and 900 °C) and the catalysts were reduced at 750 °C or 500 °C. Tuning the calcination temperature allowed for an increase in the support surface area, resulting in well-dispersed Rh species that provided a high reducibility for both the metal active phase and the Ce-based support. This allowed for an increase in methane conversion under different conditions of contact time and pressure and the outperformance of the other catalysts. The higher activity was related to well-dispersed Rh species interacting with the support that provided a high concentration of surface OH* on the Ce-based support and increased methane dissociation. This anticipated the occurrence and the extent of steam reforming over the catalytic bed, producing a smoother thermal profile.
难以减排的工艺中绿色氢的引入因用电解槽替代蒸汽重整装置的成本而受阻。然而,绿色氢可以整合到经过适当改造的重整工艺中。这里提出的工艺涉及用氧重整替代蒸汽重整,即将蒸汽重整与催化部分氧化(CPO)耦合,利用电解过程中联产的纯氧为CPO供料,由于其放热性质,这有利于更好的热交换。为了开发用于氧重整工艺的定制催化剂,通过微乳液合成了CeZrO并负载Rh。将Ce基载体在不同温度(750和900℃)下煅烧,并将催化剂在750℃或500℃下还原。调节煅烧温度可增加载体表面积,从而使Rh物种分散良好,这为金属活性相和Ce基载体都提供了高还原性。这使得在不同接触时间和压力条件下甲烷转化率提高,且性能优于其他催化剂。较高的活性与分散良好的Rh物种与载体相互作用有关,这种相互作用在Ce基载体上提供了高浓度的表面OH*并增加了甲烷解离。这提前了催化床上蒸汽重整的发生和程度,产生了更平滑的热分布。