2015
DOI: 10.1016/j.polymdegradstab.2015.09.009
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Efficient conversion of chitosan into 5-hydroxymethylfurfural via hydrothermal synthesis in ionic liquids aqueous solution

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Cited by 39 publications
(28 citation statements)
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“…The direct conversion of chitin into 5-HMF is a traditional reaction usually conducted using metal salts as catalysts (FeCl 2 , ZnCl 2 , AlCl 3 , and B(OH) 3 ) under high temperature, hydrothermal conditions (Scheme 5) (Wang et al, 2013;Yu et al, 2016). In 2015, ILs with different cations and anions of varying acidity, hydrogen-bonding capacity, and steric hindrance were tested as catalysts for 5-HMF formation from chitosan as the starting material ( (Li et al, 2015).…”
Section: Preparation Of 5-hydroxymethylfurfural (5-hmf)mentioning
confidence: 99%
“…The direct conversion of chitin into 5-HMF is a traditional reaction usually conducted using metal salts as catalysts (FeCl 2 , ZnCl 2 , AlCl 3 , and B(OH) 3 ) under high temperature, hydrothermal conditions (Scheme 5) (Wang et al, 2013;Yu et al, 2016). In 2015, ILs with different cations and anions of varying acidity, hydrogen-bonding capacity, and steric hindrance were tested as catalysts for 5-HMF formation from chitosan as the starting material ( (Li et al, 2015).…”
Section: Preparation Of 5-hydroxymethylfurfural (5-hmf)mentioning
confidence: 99%
“…Under the optimal reaction conditions (4 wt % of IL, chitosan=100 mg, 180 °C, 5 h) 29.5 mol% of HMF was obtained. With this system, chitosan with variable higher molecular weight could also be converted to HMF . In their next study they used Bronsted Lewis acidic ionic liquid ([Hmim][HSO 4 ]‐0.5FeCl 2 ).…”
Section: N‐containing Biopolymers As a Source Of Platform Chemicalsmentioning
confidence: 99%
“…With this system, chitosan with variable higher molecular weight could also be converted to HMF. [144] In their next study they used Bronsted Lewis acidic ionic liquid ([Hmim][HSO 4 ]-0.5FeCl 2 ). Addition of Lewis acidity was beneficial and it increased the yield to 44.1 %.…”
Section: N-containing Biopolymers As a Source Of Platform Chemicalsmentioning
confidence: 99%
“…An optimized 5‐HMF yield of 12.1 % was obtained at 174 °C in 2.2 wt % H 2 SO 4 solution after 37 min. Besides mineral acids, nine acidic ILs with different cations and anions were screened; the acidity, hydrogen‐bonding capacity and steric hindrance of ILs exhibited combined influences on the reaction. N ‐Methyl imidazolium hydrogen sulfate ([Mim]HSO 4 ) afforded the highest 5‐HMF yield of 29.5 % from chitosan and 19.3 % from chitin at 180 °C after 5 h. The 5‐HMF yield was the highest from chitin and chitosan among literatures reported to date.…”
Section: Chitin Conversion Into Chemicalsmentioning
confidence: 99%
“…An optimized 5-HMF yield of 12.1 %w as obtained at 174 8Ci n 2.2 wt %H 2 SO 4 solution after 37 min. Besides mineral acids, [64] nine acidic ILs with different cations and anions werescreened; the acidity,h ydrogen-bonding capacitya nd steric hindrance of An alternative transformation strategy was proposed by Hou and co-workersw ho utilized concentrated ZnCl 2 solution as the reactions olvent. [65] After optimization, 21.9 %, 2.8 %, 10.1 %, and 9.0 %y ields of 5-HMF were obtained from GlcNH 2 ,G lcNAc, low molecular weightc hitosan, and chitin, respectively,i n 67 wt %Z nCl 2 solution at 120 8Ca fter 1.5 h. Notably, the yield from GlcNAc was apparently lower,i ndicating Zn 2 + -promoted 5-HMF formation occurred by interaction with the amino group on the substrate.…”
Section: Furan Derivatives (Without Nitrogen)mentioning
confidence: 99%