Prospects of n-Butanol Production from Carbon Dioxide via Ethanol Dimerization

被引:0
|
作者
Vo, Chi Hung [1 ]
Perez-Ramirez, Javier [2 ]
Farooq, Shamsuzzaman [1 ]
Karimi, Iftekhar A. [1 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 117585, Singapore
[2] Swiss Fed Inst Technol, Inst Chem & Bioengn, Dept Chem & Appl Biosci, CH-8093 Zurich, Switzerland
来源
关键词
CO2; utilization; ethanol; butanol; Guerbet reaction; LIGNOCELLULOSIC BIOMASS; EXTRACTIVE DISTILLATION; HIGHER ALCOHOLS; CONVERSION; MEMBRANES; CATALYST; DESIGN; DEHYDRATION; SIMULATION; CHALLENGES;
D O I
10.1021/acssuschemeng.4c04769
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Higher alcohols, such as n-butanol, are promising products of CO2 utilization due to their potential uses as energy carriers or chemicals. However, their direct formation from CO2 or via syngas is hindered by low yields. Here, we designed a novel 3-step process to produce n-butanol from CO2 via syngas and ethanol. Design strategies for an ethanol-butanol-water mixture over a wide composition range have also been discussed in detail. Process performance investigation revealed that the conversion of syngas to ethanol had little effect on the total annualized cost (TAC) of n-butanol and CO2 utilization efficiency (CUE), but TAC decreased and CUE increased steadily with the increasing conversion of ethanol to n-butanol to $1739/t and 47%, respectively. Conversion to n-butanol should be at least 20% for a positive CUE and a bypass strategy around the n-butanol reactor was proposed to benefit from >40% conversion. At modest conversions in both reactors (30-40%), the H-2 cost should fall to about $600-700/t for the proposed n-butanol process from CO2 utilization to be viable. Moreover, once 30-40% Guerbet conversion is achieved, further catalysis development should focus on improving selectivity.
引用
收藏
页码:14459 / 14471
页数:13
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