TY - JOUR
T1 - Syngas production with low tar content from cellulose pyrolysis in molten salt combined with Ni/Al2O3 catalyst
AU - Ratchahat, Sakhon
AU - Srifa, Atthapon
AU - Koo-amornpattana, Wanida
AU - Sakdaronnarong, Chularat
AU - Charinpanitkul, Tawatchai
AU - Wu, Kevin C.W.
AU - Show, Pau Loke
AU - Kodama, Satoshi
AU - Tanthapanichakoon, Wiwut
AU - Sekiguchi, Hidetoshi
N1 - Funding Information:
This research work is financially supported by Department of Chemical Science and Engineering, School of Materials and Chemical Technology, Tokyo Institute of Technology, Japan. The research is also partially supported from Mahidol University (Basic Research Fund: Fiscal Year 2021, BRF1-A12/2564), Thailand.
Funding Information:
This research work is financially supported by Department of Chemical Science and Engineering , School of Materials and Chemical Technology , Tokyo Institute of Technology , Japan. The research is also partially supported from Mahidol University (Basic Research Fund: Fiscal Year 2021, BRF1-A12/2564), Thailand.
Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/9
Y1 - 2021/9
N2 - The syngas production from cellulose pyrolysis was studied in carbonate salts combined with nickel supported on alumina catalyst (MS-Ni) in a preheated reactor. Tar content was greatly reduced by 10 folds when compared to that of the pyrolysis in argon gas (Ar). Molten salt resulted in the reduction of tar and CO2 formation due to the rapid heating of 141 °C/s alter the pyrolysis pathway to produce more syngas products. Further tar elimination was promoted with the presence of nickel supported on alumina catalyst in the salt. Tar was reduced by 5 folds when compared to that the pyrolysis in sole molten salt (MS). Tar from pyrolysis in MS-Ni was about 1 wt%. In addition, CH4 could be reformed with CO2 into additional syngas over the Ni/Al2O3 catalyst. As a result, the pyrolysis in the combined salt and catalyst exhibited high syngas yield at 824 mL/g cellulose. Moreover, alumina particles enhanced the heat transfer in the molten salt, resulting in the highest heating rate of 181 °C/s obtained in MS-Ni medium. However, the catalyst deactivation was a serious issue in combining molten salt with Ni/Al2O3 catalyst. The high corrosiveness would damage the alumina support, while the Ni active metal would be leached from the catalyst particles, resulting in the catalyst deactivation.
AB - The syngas production from cellulose pyrolysis was studied in carbonate salts combined with nickel supported on alumina catalyst (MS-Ni) in a preheated reactor. Tar content was greatly reduced by 10 folds when compared to that of the pyrolysis in argon gas (Ar). Molten salt resulted in the reduction of tar and CO2 formation due to the rapid heating of 141 °C/s alter the pyrolysis pathway to produce more syngas products. Further tar elimination was promoted with the presence of nickel supported on alumina catalyst in the salt. Tar was reduced by 5 folds when compared to that the pyrolysis in sole molten salt (MS). Tar from pyrolysis in MS-Ni was about 1 wt%. In addition, CH4 could be reformed with CO2 into additional syngas over the Ni/Al2O3 catalyst. As a result, the pyrolysis in the combined salt and catalyst exhibited high syngas yield at 824 mL/g cellulose. Moreover, alumina particles enhanced the heat transfer in the molten salt, resulting in the highest heating rate of 181 °C/s obtained in MS-Ni medium. However, the catalyst deactivation was a serious issue in combining molten salt with Ni/Al2O3 catalyst. The high corrosiveness would damage the alumina support, while the Ni active metal would be leached from the catalyst particles, resulting in the catalyst deactivation.
KW - Cellulose pyrolysis
KW - Molten salt
KW - Ni/AlOcatalyst
KW - Syngastar elimination
UR - http://www.scopus.com/inward/record.url?scp=85111346253&partnerID=8YFLogxK
U2 - 10.1016/j.jaap.2021.105243
DO - 10.1016/j.jaap.2021.105243
M3 - Article
AN - SCOPUS:85111346253
SN - 0165-2370
VL - 158
JO - Journal of Analytical and Applied Pyrolysis
JF - Journal of Analytical and Applied Pyrolysis
M1 - 105243
ER -