2020
DOI: 10.1016/j.apcata.2019.117338
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Building hierarchical zeolite structure by post-synthesis treatment to promote the conversion of furanic molecules into biofuels

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Cited by 24 publications
(17 citation statements)
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“…In particular, employing the zeolite HZSM‐5 (Si/Al=25), a BEMF selectivity of 63.3 mol% was obtained at complete BHMF conversion, which was almost double of the BEMF selectivities ascertained with the acid resins. In fact, it is well known that the Brønsted acidity promotes the formation of by‐products, such as 2,5‐dihydro‐2‐ethoxy‐2‐(ethoxymethyl)‐5‐methylenefuran (DHEMMF, Figure S12) and 1‐ethoxy‐3‐hexene‐2,5‐dione (EHED, Figure S13), deriving, respectively, from the hydration of BHMF and the successive opening‐ring, as reported in Scheme S2 [20a,32–34] …”
Section: Resultsmentioning
confidence: 99%
“…In particular, employing the zeolite HZSM‐5 (Si/Al=25), a BEMF selectivity of 63.3 mol% was obtained at complete BHMF conversion, which was almost double of the BEMF selectivities ascertained with the acid resins. In fact, it is well known that the Brønsted acidity promotes the formation of by‐products, such as 2,5‐dihydro‐2‐ethoxy‐2‐(ethoxymethyl)‐5‐methylenefuran (DHEMMF, Figure S12) and 1‐ethoxy‐3‐hexene‐2,5‐dione (EHED, Figure S13), deriving, respectively, from the hydration of BHMF and the successive opening‐ring, as reported in Scheme S2 [20a,32–34] …”
Section: Resultsmentioning
confidence: 99%
“…It is also worth noting that, from HMF, ZrSi10 gives the monoether 8 as the main product. This is an interesting intermediate for the synthesis of anionic surfactants due to its residual hydroxyl group, while in the literature it is usually reported the preparation of monoether 7, [66][67][68][69][70][71][72][73] which can be used as biofuel, but having worse properties compared to the diether.…”
Section: Discussionmentioning
confidence: 99%
“…To improve the stability and the miscibility with diesel, the aldehyde group of HMF must be functionalized as an ether, making the diether the most desirable product. Whereas the production of monoethers, which has been studied quite extensively, is far easier, [66][67][68][69][70][71][72][73] the diether synthesis is troublesome, involving a reduction step prior to etherification. 51,[74][75][76] The same applies for furfural, where the preparation of ethers requires the combination of a reduction step followed by the etherification of the resulting alcohol.…”
Section: Introductionmentioning
confidence: 99%
“…The reaction of FA with (biomass-derivable) ethanol gives 2-(ethoxymethyl)furan (EMF) and ethyl levulinate (EL) (Scheme 1) [121]. The applications of EMF include bio-solvent [122], pharmaceuticals, food flavor [123][124][125][126], aging flavor for beer storage [127][128][129][130][131] or white wine [132] and fuel additive [122,[124][125][126][133][134][135][136][137] since it has a high energy density, cetane number [138] and capacity to reduce soot emissions [124,134,139,140]. On the other hand, EL is an attractive oxygenated fuel extender (its high oxygen content enhances engine efficiency, improves flow properties, etc.…”
Section: General Considerationsmentioning
confidence: 99%