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用于电热催化的可定制纳米多孔羟基磷灰石支架

Tailorable Nanoporous Hydroxyapatite Scaffolds for Electrothermal Catalysis.

作者信息

Sans Jordi, Arnau Marc, Roa Joan Josep, Turon Pau, Alemán Carlos

机构信息

Departament d'Enginyeria Química, EEBE, Universitat Politècnica de Catalunya, C/Eduard Maristany, 10-14, Ed. I2, 08019 Barcelona, Spain.

Barcelona Research Center in Multiscale Science and Engineering, Universitat Politècnica de Catalunya, C/Eduard Maristany, 10-14, 08019 Barcelona, Spain.

出版信息

ACS Appl Nano Mater. 2022 May 20;5(6):8526-8536. doi: 10.1021/acsanm.2c01915. eCollection 2022 Jun 24.

Abstract

Polarized hydroxyapatite (HAp) scaffolds with customized architecture at the nanoscale have been presented as a green alternative to conventional catalysts used for carbon and dinitrogen fixation. HAp printable inks with controlled nanoporosity and rheological properties have been successfully achieved by incorporating Pluronic hydrogel. Nanoporous scaffolds with good mechanical properties, as demonstrated by means of the nanoindentation technique, have been obtained by a sintering treatment and the posterior thermally induced polarization process. Their catalytic activity has been evaluated by considering three different key reactions (all in the presence of liquid water): (1) the synthesis of amino acids from gas mixtures of N, CO, and CH; (2) the production of ethanol from gas mixtures of CO and CH; and (3) the synthesis of ammonia from N gas. Comparison of the yields obtained by using nanoporous and nonporous (conventional) polarized HAp catalysts shows that both the nanoporosity and water absorption capacity of the former represent a drawback when the catalytic reaction requires auxiliary coating layers, as for example for the production of amino acids. This is because the surface nanopores achieved by incorporating Pluronic hydrogel are completely hindered by such auxiliary coating layers. On the contrary, the catalytic activity improves drastically for reactions in which the HAp-based scaffolds with enhanced nanoporosity are used as catalysts. More specifically, the carbon fixation from CO and CH to yield ethanol improves by more than 3000% when compared with nonporous HAp catalyst. Similarly, the synthesis of ammonia by dinitrogen fixation increases by more than 2000%. Therefore, HAp catalysts based on nanoporous scaffolds exhibit an extraordinary potential for scalability and industrial utilization for many chemical reactions, enabling a feasible green chemistry alternative to catalysts based on heavy metals.

摘要

具有纳米级定制结构的极化羟基磷灰石(HAp)支架已被视为用于碳和氮固定的传统催化剂的绿色替代品。通过加入普朗尼克水凝胶,已成功制备出具有可控纳米孔隙率和流变特性的HAp可印刷油墨。通过烧结处理和随后的热诱导极化过程,获得了具有良好机械性能的纳米多孔支架,这通过纳米压痕技术得到了证明。通过考虑三种不同的关键反应(均在液态水存在下)对其催化活性进行了评估:(1)由N、CO和CH的气体混合物合成氨基酸;(2)由CO和CH的气体混合物生产乙醇;(3)由N2气体合成氨。使用纳米多孔和无孔(传统)极化HAp催化剂获得的产率比较表明,当催化反应需要辅助涂层时,例如用于氨基酸生产时,前者的纳米孔隙率和吸水能力都成为了缺点。这是因为加入普朗尼克水凝胶实现的表面纳米孔完全被这种辅助涂层阻碍。相反,对于使用具有增强纳米孔隙率的HAp基支架作为催化剂的反应,催化活性会大幅提高。更具体地说,与无孔HAp催化剂相比,由CO和CH固定碳生成乙醇的效率提高了3000%以上。同样,通过氮固定合成氨的效率提高了2000%以上。因此,基于纳米多孔支架的HAp催化剂在许多化学反应的可扩展性和工业应用方面具有巨大潜力,为基于重金属的催化剂提供了一种可行的绿色化学替代品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43d4/9989946/237f06992cf1/an2c01915_0008.jpg

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