通过金属碳酸盐综合捕获二氧化碳并将其转化为甲烷的镧系元素促进镍催化剂

Christopher J. Koch, Zohaib Suhail, Prince, Anushan Alagaratnam, Matthew Coe, Alain Goeppert and G. K. Surya Prakash
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摘要

我们开发了一种利用金属氢氧化物盐的二氧化碳捕获和转化综合系统,以碳酸盐盐的形式从各种来源(包括空气)捕获二氧化碳,并将其直接转化为合成燃料(甲烷)。镍催化剂先前已被证明可将碳酸盐(如 K2CO3 和 Na2CO3)转化为甲烷。然而,与其他基于金属钌的催化剂相比,这些系统的生产率并不高。在镧系元素促进剂的帮助下,镍催化剂的甲烷生产率大大提高。在大多数情况下,镧系元素促进的镍催化剂的催化性能遵循镧系元素收缩的趋势,即镧系元素的原子尺寸越小,甲烷产量越高。此外,镧系元素促进的镍催化剂在所采用的碱性条件下也很稳定,在二氧化碳捕获和转化的五个循环中都能保持活性。最后,镧系元素促进的镍催化剂与钌催化剂和未促进的镍催化剂相比更经济。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Lanthanide promoted nickel catalysts for the integrated capture and conversion of carbon dioxide to methane via metal carbonates†

An integrated CO2 capture and conversion system utilizing metal hydroxide salts has been developed to capture CO2 from various sources including air in the form of carbonate salts and convert them directly into a synthetic fuel; methane. Nickel catalysts have previously been shown to convert carbonate salts, such as K2CO3 and Na2CO3, to methane. However, the productivity of these systems was rather modest in comparison to other catalysts based on ruthenium metal. With the help of lanthanide promoters, the methane productivity of nickel catalysts has been greatly improved. For the most part, the catalytic performance of the lanthanide promoted nickel catalysts followed the lanthanide contraction trend, i.e. the smaller the atomic size of the lanthanide, the higher the methane yield. Furthermore, the lanthanide promoted nickel catalysts are also stable under the alkaline conditions employed, maintaining their activity over five cycles of integrated CO2 capture and conversion. Lastly, the lanthanide promoted nickel catalysts were demonstrated to be more economical compared to ruthenium- and unpromoted nicked-based catalysts.

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Correction: Hydrothermal synthesis of ZnZrO x catalysts for CO2 hydrogenation to methanol: the effect of pH on structure and activity. Back cover Inside back cover Direct measurement of PFAS levels in surface water using an engineered biosensor. Statistical optimization of cell-hydrogel interactions for green microbiology - a tutorial review.
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