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Ethyl lactate as a solvent: Properties, applications and production processes – a review
Abstract
Ethyl lactate is an environmentally benign solvent with effectiveness comparable to petroleum-based solvents. The worldwide solvent market is about 30 million pounds per year, where ethyl lactate can have an important share. It is considered a chemical commodity and has attracted much attention in recent years, since it is formed by the esterification reaction of ethanol and lactic acid, which can be generated from biomass raw materials through fermentation. In this work, an overview regarding the main properties and applications of ethyl lactate, as well as its synthesis and production processes, with a particular emphasis on reactive/separation processes, is presented.
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“For example, alkyl lactates, the alcoholysis products of PLAs, are green substitutes for petroleumderived esters in applications such as solvents 429 or diluents for polymeric resins, 430 lowtemperature lubricants, 431 and emulsifiers or dispersants in pharmaceutical compositions.432”
From Catalysis as an Enabling Science for Sustainable Polymers (2018) · cites this paper as [429]
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Cites
Chemical Routes for the Transformation of Biomass into Chemicals
Corma, A., Iborra, S., & Velty, A. (2007) · Chemical Reviews · doi:10.1021/cr050989d · Cited by 5,970
Carbon-Negative Biofuels from Low-Input High-Diversity Grassland Biomass
Tilman, D., Hill, J., & Lehman, C. (2006) · Science · doi:10.1126/science.1133306 · Cited by 1,813
The E Factor: fifteen years on
Sheldon, R. A. (2007) · Green Chemistry · doi:10.1039/b713736m · Cited by 1,715
Green solvents for sustainable organic synthesis: state of the art
Sheldon, R. A. (2005) · Green Chemistry · doi:10.1039/b418069k · Cited by 1,713
Jessop, P. G. (2011) · Green Chemistry · doi:10.1039/c0gc00797h · Cited by 1,062
Kamm, B., & Kamm, M. (2004) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-003-1537-7 · Cited by 1,021
van Haveren, J., Scott, E. L., & Sanders, J. P. M. (2007) · Biofuels Bioproducts and Biorefining · doi:10.1002/bbb.43 · Cited by 514
Unsaturated O- and N-Heterocycles from Carbohydrate Feedstocks
Lichtenthaler, F. W. (2002) · Accounts of Chemical Research · doi:10.1021/ar010071i · Cited by 424
Sustainability Metrics: Life Cycle Assessment and Green Design in Polymers
Tabone, M. D., Cregg, J., Beckman, E. J., & Landis, A. E. (2010) · Environmental Science & Technology · doi:10.1021/es101640n · Cited by 416
Alternative Solvents: Shades of Green
Clark, J. H., & Tavener, S. J. (2006) · Organic Process Research & Development · doi:10.1021/op060160g · Cited by 406
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Research works printed but not linked: 5
- Sheldon, 1994, CHEMTECH, 38
- Wang, 2008, Int. Sugar J., 110, 527
- Reisch, 2008, Chem. Eng. News, 86, 32
- McConville, 2009, Pharm. Technol., 33, 74
- Bamoharram, 2010, React. Kinet. Mech. and Catal., 1
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Antunes, B. M., Rodrigues, A. E., Lin, Z., Portugal, I., & Silva, C. M. (2015) · Fuel Processing Technology · doi:10.1016/j.fuproc.2015.04.031 · Cited by 66
Self-citationKoutinas, M., Yiangou, C., Osório, N. M., Ioannou, K. A., Canet, A., Valero, F., & Ferreira‐Dias, S. (2017) · Bioresource Technology · doi:10.1016/j.biortech.2017.09.130 · Cited by 63
Dandia, A., Jain, A. K., & Laxkar, A. K. (2013) · Tetrahedron Letters · doi:10.1016/j.tetlet.2013.05.035 · Cited by 62
Edwards, G. A., Trafford, M. A., Hamilton, A. E., Buxton, A. M., Bardeaux, M. C., & Chalker, J. M. (2014) · The Journal of Organic Chemistry · doi:10.1021/jo402799t · Cited by 61
Alcohol acyltransferases for the biosynthesis of esters
Liu, G., Huang, L., & Lian, J. (2023) · Biotechnology for Biofuels and Bioproducts · doi:10.1186/s13068-023-02343-x · Cited by 67
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Lee, J., & Trinh, C. T. (2019) · Biotechnology for Biofuels · doi:10.1186/s13068-019-1563-z · Cited by 60
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Thi, H. Y. N., Nguyen, B. T. D., & Kim, J. F. (2020) · Membranes · doi:10.3390/membranes11010019 · Cited by 60
Tu, Q., Parvatker, A. G., Garedew, M., Harris, C., Eckelman, M. J., Zimmerman, J. B., Anastas, P. T., & Lam, J. C. (2021) · Environmental Science & Technology · doi:10.1021/acs.est.0c07309 · Cited by 59
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Designation of highly efficient catalysts for one pot conversion of glycerol to lactic acid
Tao, M., Zhang, D., Guan, H., Huang, G., & Wang, X. (2016) · Scientific Reports · doi:10.1038/srep29840 · Cited by 58
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Manic, M. S., Villanueva-Bermejo, D., Fornari, T., Queimada, A. J., Macedo, E. A., & Najdanovic‐Visak, V. (2011) · The Journal of Chemical Thermodynamics · doi:10.1016/j.jct.2011.12.005 · Cited by 58
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Wang, C., Hanindita, F., & Goto, A. (2018) · ACS Macro Letters · doi:10.1021/acsmacrolett.8b00026 · Cited by 54
Rubab, L., Anum, A., Al‐Hussain, S. A., Irfan, A., Ahmad, S., Ullah, S., Al‐Mutairi, A. A., & Zaki, M. E. A. (2022) · Catalysts · doi:10.3390/catal12111329 · Cited by 56
Purushothaman, R. K. P., van Haveren, J., Melián-Cabrera, I. V., van Eck, E. R. H., & Heeres, H. J. (2014) · ChemSusChem · doi:10.1002/cssc.201301105 · Cited by 54
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Nguyen, V. C., Bui, N. Q., Mascunan, P., Vu, T. T. H., Fongarland, P., & Essayem, N. (2018) · Applied Catalysis A General · doi:10.1016/j.apcata.2017.12.024 · Cited by 54
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Yue, Y., Zhang, Z., Bak, S., Yao, S., Hu, X., Shadike, Z., Do‐Thanh, C., Zhang, F., Chen, H., Lyu, X., et al. (2018) · ACS Catalysis · doi:10.1021/acscatal.8b03230 · Cited by 53
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Wan, J., Wang, C., Zhou, R., & Liu, Y. (2012) · RSC Advances · doi:10.1039/c2ra21632a · Cited by 52
Tripathi, S., Kapoor, R., & Yadav, L. D. S. (2018) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.201701559 · Cited by 52
Payne, J., McKeown, P., Driscoll, O. J., Kociok-Köhn, G. I., Emanuelsson, E. A. C., & Jones, M. D. (2021) · Polymer Chemistry · doi:10.1039/d0py01519a · Cited by 48
Anila, P., Reddy, K. R., Rao, G. S., Sairam, P. V. S., Ramachandran, D., & Rambabu, C. (2015) · Thermochimica Acta · doi:10.1016/j.tca.2015.09.021 · Cited by 50
Yıldırım, S., Demirtaş, T. T., Dinçer, C. A., Yıldız, N., & Karakeçili, A. G. (2017) · The Journal of Supercritical Fluids · doi:10.1016/j.supflu.2017.10.009 · Cited by 49
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Ruiz, D., Michel, V. F., Niederberger, M., & Lizundia, E. (2023) · Small · doi:10.1002/smll.202303394 · Cited by 49
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Sutter, M., Pehlivan, L., Lafon, R., Dayoub, W., Raoul, Y., Métay, E., & Lemaire, M. (2013) · Green Chemistry · doi:10.1039/c3gc41082j · Cited by 45
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Pagano, I., Sánchez‐Camargo, A. D. P., Mendiola, J. A., Campone, L., Cifuentes, A., Rastrelli, L., & Ibáñez, E. (2018) · Electrophoresis · doi:10.1002/elps.201700442 · Cited by 40
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Kausar, N., Masum, A. A., Islam, M. M., & Das, A. R. (2017) · Molecular Diversity · doi:10.1007/s11030-017-9728-9 · Cited by 33
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Zhou, X., Liu, Q., Xu, G., Yang, R., Sun, H., & Wang, Q. (2023) · Chinese Chemical Letters · doi:10.1016/j.cclet.2023.108158 · Cited by 32
Moussallem, C., Gohier, F., Mallet, C., Allain, M., & Frère, P. (2012) · Tetrahedron · doi:10.1016/j.tet.2012.07.079 · Cited by 33
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Watson, A. J. B., Wilson, K., Murray, J., Sneddon, H. F., & Jamieson, C. (2018) · Synlett · doi:10.1055/s-0037-1611054 · Cited by 31
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Decroix, C., Chalamet, Y., Sudre, G., & Vergelati, C. (2020) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2020.116072 · Cited by 29
Shen, H., Zhou, Y., Wen, G., Xu, L., Ding, Q., Guan, Y., Yang, Z., Sun, Y., Gao, X., Zhang, J., et al. (2022) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2022.106552 · Cited by 29
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Kamalanathan, I. D., Canal, L., Hegarty, J., & Najdanovic‐Visak, V. (2018) · Fluid Phase Equilibria · doi:10.1016/j.fluid.2018.01.016 · Cited by 28
Oh, J., Sreedhar, B., Donaldson, M. E., Frank, T. C., Schultz, A. K., Bommarius, A. S., & Kawajiri, Y. (2016) · Journal of Chromatography A · doi:10.1016/j.chroma.2016.08.072 · Cited by 27
Álvarez, I., Gutiérrez, C., Rodríguez, J. F., de Lucas, A., & García, M. T. (2020) · Journal of CO2 Utilization · doi:10.1016/j.jcou.2020.101227 · Cited by 27
Wouwe, P. V., Dusselier, M., Basiç, A., & Sels, B. F. (2013) · Green Chemistry · doi:10.1039/c3gc41457d · Cited by 29
Salerno, A., Fernández‐Gutiérrez, M., del Barrio, J. S. R., & Domingo, C. (2014) · RSC Advances · doi:10.1039/c4ra07732f · Cited by 27
Metadata
- Authors
- Pereira, C. S. M., Silva, V. M. T. M., & Rodrigues, A. E.
- Affiliations
- Universidade do Porto (PT)
- Corresponding author
- Silva, Viviana M. T. M.
- Venue
- Green Chemistry
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2011
- Volume
- 13
- Issue
- 10
- Pages
- 2658
- ISSN
- 1463-9262 (ISSN-L)
- 1463-9270
- OpenAlex
- W2041169847
- Cited by
- 544
- References
- 64
- Citations by year
- 2026: 27 · 2025: 52 · 2024: 47 · 2023: 41 · 2022: 40 · 2021: 40 · 2020: 42 · 2019: 34 · 2018: 44 · 2017: 31 · 2016: 25 · 2015: 41 · 2014: 32 · 2013: 31 · 2012: 15
- FWCI
- 15.17
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Green Chemistry (publishedVersion)
- Funders
- U.S. Food and Drug Administration
- Topics
- Physical Sciences › Chemical Engineering › Catalysis › Catalysis for Biomass Conversion
- Physical Sciences › Environmental Science › Environmental Chemistry › Chemistry and Chemical Engineering
- Physical Sciences › Chemistry › Organic Chemistry › Chemical Synthesis and Reactions
- Keywords
- ethyl lactate, green solvents, solvent properties, solvent applications, solvent production, bio-based chemicals, fermentation
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