Cellulose Alcoholysis to Alkyl-levulinate Biofuels: History
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Subjects: Chemistry, Applied
Contributor:
Anna Maria Raspolli Galletti
,
Claudia Antonetti
,
Sara Fulignati
,
Domenico Licursi

Alkyl levulinates (ALs) represent outstanding bio-fuels and strategic bio-products within the context of the marketing of levulinic acid derivatives. In order to promote the market for these bio-products and, concurrently, the immediate development of new applications, it is necessary to speed up the intensification of their production processes. In this regard, today, it is possible to achieve this important issue only by using low-cost or, even better, waste biomasses, as starting feedstocks. Thus, the transition to the real biomass now represents a necessary choice for allowing the next ALs production on a larger scale. The improvement of the available synthetic strategies, the use of raw materials and the development of new applications for ALs can contribute to develop more intensified, greener and sustainable processes. 

  • Alkyl levulinates
  • One-pot alcoholysis
  • Solvothermal processes
  • Levulinic acid
  • Bio-fuels
  • Process intensification

1. Introduction

Alkyl levulinates (ALs) are valuable chemicals having strong market potential, mainly as oxygenated bio-fuels. ALs can be produced via dehydration of C6 carbohydrates, such as glucose or fructose, carried out in the presence of acid catalyst and alcohols as reaction medium.[1] In this context, also the direct transformation of model and real cellulose-based feedstocks into ALs has been proposed and demonstrated, the last one resulting certainly more advantageous than that of simpler pure carbohydrates, especially when low-cost or waste biomasses are used as starting feedstock.[2] The overall C6-pathway occurs via etherification of the starting C6 carbohydrates, their next transformation into the corresponding 5-hydroxymethylfurfural-ether derivative, and subsequent rehydration of the latter to give the desired AL.[3] In the presence of alcohol medium, the formation of furanic by-products, known as humins, is greatly reduced respect to the corresponding hydrothermal process for levulinic acid production, thus leading to higher yields and selectivities to ALs.[4] C6-pathway is certainly more performing starting from simpler model sugars (rather than cellulose or real biomass), homogeneous catalysts (rather than heterogeneous ones) and shorter-chain alcohols. For example, in the case of methyl levulinate production, the highest yield of about 90 mol% was obtained by Feng et al.[5] starting from fructose and adopting sulfuric acid as homogeneous catalyst. On the other hand, lower yields (up to 70 mol%) were obtained by other authors starting from glucose or cellulose, due to the greater difficulty of their conversion, caused by the additional isomerization step from glucose to fructose, which is generally favoured by Lewis acids, and by the greater recalcitrance of cellulose.[6] To a greater complexity, lignocellulosic biomass (such as bamboo, straw, eucalyptus, poplar, pine and bagasse) is even more difficult to convert, mainly due to the presence of the lignin component, leading to methyl levulinate (ML) yields up to 35 mol%.[5] On this basis, many homogeneous/heterogeneous catalysts have been proposed, such as sulfonic acids, sulfonate salts (in particular, triflates), polyoxometalates, zeolites, montmorillonites and metal oxides, by alone or in some combinations, in order to balance the Brønsted-Lewis acidities, thus directing the reaction towards the AL production, rather than those of other reaction products, such as humins, alkyl lactate and 1,1,2-trialkoxyethane.[2] 

In addition to the alcoholysis of C6-feedstocks, occurring in the presence of alcohols and acid catalysts, synthetic strategies via 5-chloromethylfurfural and subsequent heating in the desired alcohol or utilizing furfuryl alcohol as starting feedstocks, have been proposed and demonstrated.[7] While 5-chloromethylfurfural may be obtained in one-step from cellulose, furfuryl alcohol pathway employs hemicellulose as starting feedstock, thus bridging the C5 and C6 carbohydrate value chain, very promising in a biorefinery perspective.

2. Possible ALs Applications

Regarding the possible applications of ALs, in principle, they can be used as biofuels, biofuel additives, green solvents, flavoring agents, lubricants, fragrances and polymer plasticizer.[8][9] The use of short-chain ALs, in particular, ML and ethyl levulinate (EL), as sustainable oxygenated fuel-additives, has been deeply investigated, resulting in being really promising for this purpose.[8][9] Shrivastav et al.[10] blended C1-C4 ALs with conventional gasoline fuel maintaining up to 18 mol%, density, viscosity and compressibility within the recommended limits. The tested ALs showed good octane ratings, similar C/H ratio to that of aromatics and better local oxygen concentration than that of traditional methyl tert-butyl ether. The authors increased the amount of the blended ALs up to 35 mol%, reducing the aromatic content of gasoline. However, low-chain ALs suffer from some limitations, including high oxygen content, good water solubility and low-energy density. For this reason, new research trends are rather directed towards the synthesis of longer-chain ALs with higher carbon content and stronger hydrophobicity, thus improving the energy density and water insolubility. These “biodiesel-like” ALs result in being more appropriate as oxygenated additives for diesel blends.[11][12][13][14][15] However, given the more difficult synthesis of the levulinates with increasing length of the alcohol residue, only a few papers are reported for these esters, mostly synthesized starting from the more costly and pure levulinic acid, often preferring elegant catalysts, which have been synthesized ad hoc on the laboratory scale. In order to increase the development of high-volume automotive applications, it is necessary to find a compromise between the synthesis of these bio-products, which should be easily achievable, and their motor performances, which should be (at least) satisfactory. Up to now, butyl levulinate (BL) meets both of these requirements, due to its feasible synthesis, even starting from real biomasses, and to the related good diesel performances, also allowing for a significant reduction of both CO and soot emissions.[16] In this context, Kremeret al.[17] have discussed in detail the engineering aspects that are related to the motor applications of this levulinate, also positively re-evaluating those of the di-n-butyl ether. This last compound, which is obtained as the main by-product from the same alcoholysis process, can be used, in addition to a pure diesel alternative, as an ignition enhancer for low-cetane biofuels, due to its high self-ignitability (Cetane Number = 100). In principle, alcoholysis can be applied as mild biomass pre-treatment, in a biorefinery perspective, such as for the selective depolymerization/liquefaction of its main components, cellulose, hemicellulose, and lignin. All of them can be effectively fractionated and converted into valuable bioproducts, such as not only ALs but also alkyl glucosides/xylosides and soluble aromatics to be used for niche added-value applications.[18][19][20] In particular, the use of long-chain alkyl glucosides as bio-surfactants has been widely demonstrated, showing the remarkable advantages of performance, biodegradability, low-toxicity and environmental compatibility.[21][22] On the other hand, alcoholysis also enables the breakdown of ether linkages of lignin, in order to give smaller aromatics,[23][24] which can be isolated and further functionalized to more value-added products, such as polymer building blocks/pharmaceuticals, or defunctionalized to simpler drop-in molecules (BTX, phenol, catechol, and cyclohexane), which have a large market potential.[25]

This entry is adapted from the peer-reviewed paper 10.3390/catal10101221

References

  1. Xiaofang Liu; Wenjia Yang; Qiuyun Zhang; Can Li; Hongguo Wu; Current Approaches to Alkyl Levulinates via Efficient Valorization of Biomass Derivatives. Frontiers in Chemistry 2020, 8, 794, 10.3389/fchem.2020.00794.
  2. Anna Maria Raspolli Galletti; Claudia Antonetti; Sara Fulignati; Domenico Licursi; Direct Alcoholysis of Carbohydrate Precursors and Real Cellulosic Biomasses to Alkyl Levulinates: A Critical Review. Catalysts 2020, 10, 1221, 10.3390/catal10101221.
  3. DaQian Ding; Jinxu Xi; Jianjian Wang; Xiaohui Liu; Guanzhong Lu; Yanqin Wang; Production of methyl levulinate from cellulose: selectivity and mechanism study. Green Chemistry 2015, 17, 4037-4044, 10.1039/c5gc00440c.
  4. Ning Shi; Qiying Liu; Hu Cen; Rongmei Ju; Xiong He; Longlong Ma; Formation of humins during degradation of carbohydrates and furfural derivatives in various solvents. Biomass Conversion and Biorefinery 2019, 10, 277-287, 10.1007/s13399-019-00414-4.
  5. Junfeng Feng; Jianchun Jiang; Chung-Yun Hse; ZhongZhi Yang; Kui Wang; Jun Ye; Junming Xu; Selective catalytic conversion of waste lignocellulosic biomass for renewable value-added chemicals via directional microwave-assisted liquefaction. Sustainable Energy & Fuels 2018, 2, 1035-1047, 10.1039/c7se00579b.
  6. Xueli Chen; Yuxuan Zhang; Tao Hou; Lujia Han; Weihua Xiao; Catalysis performance comparison of a Brønsted acid H 2 SO 4 and a Lewis acid Al 2 (SO 4 ) 3 in methyl levulinate production from biomass carbohydrates. Journal of Energy Chemistry 2018, 27, 552-558, 10.1016/j.jechem.2017.11.005.
  7. Sharath Bandibairanahalli Onkarappa; Navya Subray Bhat; Saikat Dutta; Preparation of alkyl levulinates from biomass-derived 5-(halomethyl)furfural (X = Cl, Br), furfuryl alcohol, and angelica lactone using silica-supported perchloric acid as a heterogeneous acid catalyst. Biomass Conversion and Biorefinery 2020, 10, 1-8, 10.1007/s13399-020-00791-1.
  8. Kirtikumar C. Badgujar; Vivek C. Badgujar; Bhalchandra M. Bhanage; A review on catalytic synthesis of energy rich fuel additive levulinate compounds from biomass derived levulinic acid. Fuel Processing Technology 2020, 197, 106213, 10.1016/j.fuproc.2019.106213.
  9. Alexandre Démolis; Nadine Essayem; Franck Rataboul; Synthesis and Applications of Alkyl Levulinates. ACS Sustainable Chemistry & Engineering 2014, 2, 1338-1352, 10.1021/sc500082n.
  10. Gourav Shrivastav; Tuhin Suvra Khan; Manish Agarwal; Mohammad Ali Haider; Reformulation of Gasoline To Replace Aromatics by Biomass-Derived Alkyl Levulinates. ACS Sustainable Chemistry & Engineering 2017, 5, 7118-7127, 10.1021/acssuschemeng.7b01316.
  11. Earl Christensen; Aaron Williams; Stephen Paul; Steve Burton; Robert L. McCormick; Properties and Performance of Levulinate Esters as Diesel Blend Components. Energy & Fuels 2011, 25, 5422-5428, 10.1021/ef201229j.
  12. Mahsasadat Mortazavi Tabrizi; Alireza Najafi Chermahini; Zahra Mohammadbagheri; Synthesis of hexyl levulinate as a potential fuel additive from levulinic acid over a solid acid catalyst. Journal of Environmental Chemical Engineering 2019, 7, 103420–103426, 10.1016/j.jece.2019.103420.
  13. Songyan Jia; Jiao Ma; Dongping Wang; Kangjun Wang; Qiang Zheng; Chunshan Song; Xinwen Guo; Fast and efficient upgrading of levulinic acid into long-chain alkyl levulinate fuel additives with a tungsten salt catalyst at low temperature. Sustainable Energy & Fuels 2020, 4, 2018-2025, 10.1039/c9se01287g.
  14. Kajal S. Jaiswal; Virendra K. Rathod; Green synthesis of amyl levulinate using lipase in the solvent free system: Optimization, mechanism and thermodynamics studies. Catalysis Today 2020. In press 10.1016/j.cattod.2020.06.059
  15. Chandrakant Mukesh; Dariush Nikjoo; Jyri-Pekka Mikkola; Production of C-14 Levulinate Ester from Glucose Fermentation Liquors Catalyzed by Acidic Ionic Liquids in a Solvent-Free Self-Biphasic System. ACS Omega 2020, 5, 4828-4835, 10.1021/acsomega.9b03517.
  16. Claudia Antonetti; Samuele Gori; Domenico Licursi; Gianluca Pasini; Stefano Frigo; Mar López; Juan Carlos Parajó; Anna Maria Raspolli Galletti; One-Pot Alcoholysis of the Lignocellulosic Eucalyptus nitens Biomass to n-Butyl Levulinate, a Valuable Additive for Diesel Motor Fuel. Catalysts 2020, 10, 509, 10.3390/catal10050509.
  17. Florian Kremer; Stefan Pischinger. Butyl ethers and levulinates; Michael Boot, Eds.; Wiley-VCH GmbH & Co. KGaA: Weinheim, Germany, 2016; pp. 87–104.
  18. Yan Ma; Weihong Tan; Kui Wang; Jingxin Wang; Jianchun Jiang; Junming Xu; An Insight into the Selective Conversion of Bamboo Biomass to Ethyl Glycosides. ACS Sustainable Chemistry & Engineering 2017, 5, 5880-5886, 10.1021/acssuschemeng.7b00618.
  19. Chun Chang; Lin Deng; Guizhuan Xu; Efficient conversion of wheat straw into methyl levulinate catalyzed by cheap metal sulfate in a biorefinery concept. Industrial Crops and Products 2018, 117, 197-204, 10.1016/j.indcrop.2018.03.009.
  20. Yan Ma; Jingxin Wang; Weihong Tan; Jianchun Jiang; Junming Xu; Kui Wang; Directional liquefaction of lignocellulosic biomass for value added monosaccharides and aromatic compounds. Industrial Crops and Products 2019, 135, 251-259, 10.1016/j.indcrop.2019.04.038.
  21. Louise Renault; Freddy Pessel; Thierry Benvegnu. Surfactants based on green/blue sugars: Towards new functionalities in formulations; Amelia Pilar Rauter; Thisbe Lindhorst; Yves Queneau, Eds.; RSC: Croydon, UK, 2018; pp. 196–244.
  22. Jinyang Chen; Jinrui Li; Kaiyu Liu; Menghan Hong; Rong You; Peipei Qu; Meilin Chen; Subcritical Methanolysis of Starch and Transglycosidation to Produce Dodecyl Polyglucosides. ACS Omega 2019, 4, 16372-16377, 10.1021/acsomega.9b01617.
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  24. Fang Wang; You-Zhu Yu; Yigang Chen; Chun-Yu Yang; Yuan-Yu Yang; One-step alcoholysis of lignin into small-molecular aromatics: Influence of temperature, solvent, and catalyst. Biotechnology Reports 2019, 24, e00363, 10.1016/j.btre.2019.e00363.
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