TY - JOUR
T1 - Modeling of nickel-based hydrotalcite catalyst coated on heat exchanger reactors for CO2 methanation
AU - Vidal Vázquez, Francisco
AU - Kihlman, Johanna
AU - Mylvaganam, Ajenthan
AU - Simell, Pekka
AU - Koskinen-Soivi, Mari Leena
AU - Alopaeus, Ville
N1 - Funding Information:
Business Finland founding agency is acknowledged for the financial support in the SOLETAIR project (www.soletair.fi). Project partners of the SOLETAIR project are also acknowledged for their financial support.
Publisher Copyright:
© 2018 Elsevier B.V.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2018/10/1
Y1 - 2018/10/1
N2 - This study presents the kinetic modeling of CO2 methanation reaction using 15 wt% Ni/Mg/Al hydrotalcite coated catalyst. Power law and Langmuir-Hinshelwood-Hougens-Watson (LHHW) models were used to represent the kinetics of CO2 methanation. LHHW model displayed better representation of the kinetics and was chosen for modeling the CO2 methanation reaction in a plate type heat exchanger reactor. Comparison between experiments, 1D model, and 2D model proved the reliability of using internally coated tubular reactor for kinetic modeling of coated catalyst. This work also performed modeling of a plate type heat exchanger reactor with catalytically coated corrugated plates for CO2 methanation. Heat exchanger reactors with coated catalyst allow controlling the reaction temperature and thus, avoiding temperature runaway owing to the highly exothermic CO2 methanation reaction. The corrugated pattern created by the opposing corrugated plates of the plate heat exchanger reactor proved to be excellent for distributing the flow homogeneously inside each reaction channel and the entire reactor. In this reactor, 92% CO2 conversion was achieved at GHSV = 4400 h−1, 573 K and 5 bar. The good performance of this reactor was due to the high activity displayed by Ni-hydrotalcite coated catalyst, homogeneous flow distribution and high surface area of the reactor. Thus, plate type heat exchanger reactor with catalytically coated corrugated plates proved to be suitable alternative to plate heat exchanger reactors with microchannel plates.
AB - This study presents the kinetic modeling of CO2 methanation reaction using 15 wt% Ni/Mg/Al hydrotalcite coated catalyst. Power law and Langmuir-Hinshelwood-Hougens-Watson (LHHW) models were used to represent the kinetics of CO2 methanation. LHHW model displayed better representation of the kinetics and was chosen for modeling the CO2 methanation reaction in a plate type heat exchanger reactor. Comparison between experiments, 1D model, and 2D model proved the reliability of using internally coated tubular reactor for kinetic modeling of coated catalyst. This work also performed modeling of a plate type heat exchanger reactor with catalytically coated corrugated plates for CO2 methanation. Heat exchanger reactors with coated catalyst allow controlling the reaction temperature and thus, avoiding temperature runaway owing to the highly exothermic CO2 methanation reaction. The corrugated pattern created by the opposing corrugated plates of the plate heat exchanger reactor proved to be excellent for distributing the flow homogeneously inside each reaction channel and the entire reactor. In this reactor, 92% CO2 conversion was achieved at GHSV = 4400 h−1, 573 K and 5 bar. The good performance of this reactor was due to the high activity displayed by Ni-hydrotalcite coated catalyst, homogeneous flow distribution and high surface area of the reactor. Thus, plate type heat exchanger reactor with catalytically coated corrugated plates proved to be suitable alternative to plate heat exchanger reactors with microchannel plates.
KW - Carbon capture and utilization
KW - CO methanation
KW - Coated catalyst
KW - Heat exchanger reactor
KW - Hydrotalcite
KW - Reactor modeling
UR - http://www.scopus.com/inward/record.url?scp=85047395369&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2018.05.119
DO - 10.1016/j.cej.2018.05.119
M3 - Article
AN - SCOPUS:85047395369
SN - 1385-8947
VL - 349
SP - 694
EP - 707
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
ER -