High-purity hydrogen production from phenol on Ni-CaO-Ca12Al14O33 multifunctional catalyst derived from recovered layered double hydroxide

氢氧化物 催化作用 吸附 苯酚 烧结 化学工程 吸附 制氢 材料科学 解吸 多孔性 纳米颗粒 碳纤维 无机化学 化学 纳米技术 有机化学 冶金 复合材料 复合数 工程类
作者
Chengxiong Dang,Shuling Liang,Wenwen Yang,Weiquan Cai
出处
期刊:Fuel [Elsevier BV]
卷期号:332: 126041-126041 被引量:12
标识
DOI:10.1016/j.fuel.2022.126041
摘要

A recovery approach of Ni-Ca-Al layered double hydroxide (LDH) structure is developed to produce wormhole-like Ni-CaO-Ca 12 Al 14 O 33 bifunctional catalyst, which exhibits excellent stability in sorption-enhanced steam reforming of phenol for producing high-purity H 2 . • The multifunctional catalyst is prepared from rehydrated layered double hydroxide. • Adsorbed tetracycline forms carbon template to achieve a wormhole-like structure. • 98.3 vol% H 2 is stably produced from phenol with CO 2 capture in 50 cyclic tests. Hydrogen production with in situ CO 2 capture by the sorption-enhanced steam reforming (SESR) technology is a promising concept to reduce anthropogenic CO 2 emissions. A serious disadvantage of SESR processes is the rapid, sintering-induced decay of its cyclic performance. Here, a recovery approach of Ni-Ca-Al layered double hydroxide (LDH) structure with adsorbed tetracycline to develop a multifunctional catalyst is exploited. The in situ formation of carbon template originating from the adsorbed tetracycline allows for the emergence of favorable structure possessing excess porosity along with deposition of small nanoparticles, thus providing physical isolation to inhibit the sintering of Ca and Ni species. As such, 98.3 vol% H 2 was stably produced from phenol in 50 cyclic tests, during which only 33 % decrease of sorption-enhancement effect was observed, ensuring superior SESR of phenol performance. This strategy provides a new paradigm for the rational design of materials derived from LDH for high-temperature reactions.
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