Valorization of carbonaceous co-product obtained from iron ore-catalyzed methane cracking as support for Pd catalysts in toluene hydrogenation reaction

被引:0
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作者
Rios, Jaime Lopez-de los [1 ]
Torres, Daniel [1 ]
Di Stasi, Christian [1 ]
Ayala-Cortes, Alejandro [1 ]
Suelves, Isabel [1 ]
Pinilla, Jose Luis [1 ]
机构
[1] CSIC, Inst Carboquim, C-Miguel Luesma Castan,4, Zaragoza 50018, Spain
来源
关键词
Methane catalytic cracking; Toluene hydrogenation; Carbon-based catalyst; Iron ore valorization; Acid functionalization; LOW-LOADING PD; DECOMPOSITION; BENZENE; HYDROISOMERIZATION; ENHANCEMENT; CYCLOHEXENE; PERFORMANCE; REDUCTION; NANOTUBES; COMPLEXES;
D O I
10.1016/j.jece.2024.114602
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Iron ore has been proven as an abundant and sustainable catalyst in the production of hydrogen by catalytic cracking of methane. One of the main challenges is the identification of suitable market niches for the utilization of the resulting iron-carbon hybrid in order to make this process economically viable. This study examines the feasibility of using the iron-carbon hybrid obtained from methane cracking as support of Pd catalysts for the hydrogenation of toluene (350 degrees C, 35 bar of H2 at room temperature and 90 min). Before supporting Pd, Fe-C hybrid was subjected to different acid functionalization treatments (nitric and/or phosphoric acids). The results indicate that sequential oxidation with nitric acid, followed by phosphoric acid, is the most effective strategy for achieving the highest catalytic activity (1294 mmolToluene gPd-1) and conversion (27 %). Toluene conversion was 1.8 and 14.2 times higher than with the catalysts treated with nitric and phosphoric acid separately. Therefore, this work proves the possibility of employing carbon/Fe hybrid materials obtained in iron ore catalyzed methane cracking as catalytic supports in industrial relevant reactions.
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页数:11
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