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Received April 2, 2020
Accepted May 27, 2020
- This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Efficient conversion of glucosamine to ethyl levulinate catalyzed by methanesulfonic acid
Department of Biotechnology, School of Marine and Fisheries Life Science, Pukyong National University, Busan 48513, Korea
gtjeong@pknu.ac.kr
Korean Journal of Chemical Engineering, October 2020, 37(10), 1743-1750(8), 10.1007/s11814-020-0594-2
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Abstract
This study is focused on the possibility of using crustacean waste shells for sustainable biofuels and chemical production. We investigated the synthesis of ethyl levulinate (EL) from glucosamine by the methanesulfonic acidcatalyzed hydrothermal reaction using Box-Behnken design. In the ethyl levulinate synthesis, higher water content highly inhibited the formation of EL. Among the reaction factors, reaction temperature, catalyst concentration, and reaction time positively affected the outcome more than substrate concentration. The optimized reaction conditions were 200 °C reaction temperature, 60 g/L substrate concentration, 0.75M catalyst concentration, and 44.9min. Under these conditions, a 22.76mol% EL yield was achieved. These results suggest that crustacean waste shells can be used for renewable feedstocks to produce valuable chemicals and biofuels.
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References
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Kim HS, Park MR, Kim SK, Jeong GT, Korean J. Chem. Eng., 35(6), 1290 (2018)
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Coh BY, Lee JW, Kim ES, Park YS, J. Chitin Chitosan, 8(3), 127 (2003)
Hulsey MJ, Green Energy Environ., 3, 318 (2018)
Tiong YW, Yap CL, Gan S, Yap WSP, Ind. Crop. Prod., 128, 221 (2019)
Quereshi S, Ahmad E, Pant KK, Dutta S, Catal. Today, 291, 187 (2017)
Chang C, Xu GZ, Jiang XX, Bioresour. Technol., 121, 93 (2012)
Peng LC, Lin L, Zhang JH, Shi JB, Liu SJ, Appl. Catal. A: Gen., 397(1-2), 259 (2011)
Ahmad E, Alama MI, Pant KK, Haider MA, Green Chem., 18, 4804 (2016)
Guan Q, Lei T, Wang Z, Xu H, Lin L, Chen G, Li X, Li Z, Ind. Crop. Prod., 113, 150 (2018)
Bozell JJ, Petersen GR, Green Chem., 12(4), 539 (2010)
Popova M, Shestakova P, Lazarova H, Dimitrov M, Kovacheva D, Szegedi A, Mali G, Dasireddy V, Likozar B, Wilde N, Glaser R, Appl. Catal. A: Gen., 560, 119 (2018)
Pasquale G, Vazquez P, Romanelli G, Baronetti G, Catal. Commun., 18, 115 (2012)
Zhang Z, Dong K, Zhao ZK, ChemSusChem, 4, 112 (2011)
Park MR, Kim HS, Kim SK, Jeong GT, Fuel Process. Technol., 172, 115 (2018)
Miller GL, Anal. Chem., 31, 426 (1959)
Xu G, Chang C, Fang S, Ma X, Renew. Energy, 78, 583 (2015)
Rataboul F, Essayem N, Ind. Eng. Chem. Res., 50(2), 799 (2011)
Mascal M, Nikitin EB, ChemSusChem, 3, 1349 (2010)
De S, Dutta S, Saha B, Green Chem., 13, 2859 (2011)
Zhao G, Liu M, Xia X, Li L, Xu B, Molecules, 24, 1881 (2019)
Omari KW, Besaw JE, Kerton FM, Green Chem., 14, 1480 (2012)