2016
DOI: 10.1134/s1070428016060014
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Technological aspects of fructose conversion to high-purity 5-hydroxymethylfurfural, a versatile platform chemical

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Cited by 30 publications
(10 citation statements)
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“…[77] Am ixture of Na 2 SO 4 ·10 H 2 O( 467 g, 1.45 mol) and 98 wt %H 2 SO 4 (105 g, 1.05 mol) was heated to 85 8C, then fructose (100 g, 0.56 mol) and methyl isobutyl ketone (1.0 L) were added while stirring, and the mixture was vigorously stirred for 2hat 85 8C. [77] Am ixture of Na 2 SO 4 ·10 H 2 O( 467 g, 1.45 mol) and 98 wt %H 2 SO 4 (105 g, 1.05 mol) was heated to 85 8C, then fructose (100 g, 0.56 mol) and methyl isobutyl ketone (1.0 L) were added while stirring, and the mixture was vigorously stirred for 2hat 85 8C.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…[77] Am ixture of Na 2 SO 4 ·10 H 2 O( 467 g, 1.45 mol) and 98 wt %H 2 SO 4 (105 g, 1.05 mol) was heated to 85 8C, then fructose (100 g, 0.56 mol) and methyl isobutyl ketone (1.0 L) were added while stirring, and the mixture was vigorously stirred for 2hat 85 8C. [77] Am ixture of Na 2 SO 4 ·10 H 2 O( 467 g, 1.45 mol) and 98 wt %H 2 SO 4 (105 g, 1.05 mol) was heated to 85 8C, then fructose (100 g, 0.56 mol) and methyl isobutyl ketone (1.0 L) were added while stirring, and the mixture was vigorously stirred for 2hat 85 8C.…”
Section: Methodsmentioning
confidence: 99%
“…Humins were obtained as byproducts of HMF synthesis from fructose in ab iphasic system (aqueous NaHSO 4 /methyl isobutyl ketone). [77] Am ixture of Na 2 SO 4 ·10 H 2 O( 467 g, 1.45 mol) and 98 wt %H 2 SO 4 (105 g, 1.05 mol) was heated to 85 8C, then fructose (100 g, 0.56 mol) and methyl isobutyl ketone (1.0 L) were added while stirring, and the mixture was vigorously stirred for 2hat 85 8C. The resulting mixture was cooled to 30 8C, the aqueous and organic layers were separated by decantation.…”
Section: Synthesis Of Hmf and Formation Of Huminsmentioning
confidence: 99%
“…[85] This is also reflected in al arge number of reports dedicated to the catalytic conversion of carbohydrates into HMF by using typical acidic resins, functionalized silica, zeolites, heteropolyacids, and other solids. [86][87][88] Notwithstanding the ability to recover heterogeneous catalysts by filtration, homogeneous catalysts can often be efficiently recovered by the simple removal of the organic phase, which containsp roducts, [84,89] leaving the acid catalyst in the aqueous phase. On the other hand, solid acids are frequently disposedofdue to their irreversible deactivation by the formation of byproduct polymer humins on their surface.…”
Section: Hmf and Its Derivativesmentioning
confidence: 99%
“… General overview of synthetic sequence to access HMF, [16] FDCA, [17] OBMF, OBFA, diallylfuran‐2,5‐dicarboxylate (DAF) and diallyl 5,5'‐oxybis(methylene) bis [furan‐2‐carboxylate] (DADF) [14d] …”
Section: Resultsmentioning
confidence: 99%