2021
DOI: 10.1016/j.ecmx.2021.100141
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Green synthesis of 5-hydroxymethylfurfural through non-catalytic conversion of glucose in a microreactor

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Cited by 6 publications
(12 citation statements)
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“…But above the optimum value, the contamination of MIBK with water also increased which further enhanced the hydration of HMF present in the MIBK phase, which was contaminated with water, thereby decreasing HMF yield and selectivity . Another problem with a very high organic phase-to-aqueous phase ratio is the reduced mass-transfer area between the organic and aqueous phases . Furthermore, a very high residence time in a microreactor decreases the HMF yield, because of the dehydration of HMF into levulinic acid …”
Section: Hmf Synthesis From Sugarsmentioning
confidence: 99%
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“…But above the optimum value, the contamination of MIBK with water also increased which further enhanced the hydration of HMF present in the MIBK phase, which was contaminated with water, thereby decreasing HMF yield and selectivity . Another problem with a very high organic phase-to-aqueous phase ratio is the reduced mass-transfer area between the organic and aqueous phases . Furthermore, a very high residence time in a microreactor decreases the HMF yield, because of the dehydration of HMF into levulinic acid …”
Section: Hmf Synthesis From Sugarsmentioning
confidence: 99%
“…42 However, it is important to not use excess organic phase volume because it leads to a decrease in the HMF yield. 44 Excess organic phase results in H 2 O entering into the organic phase with the catalyst, which again promotes side reactions in the organic phase and decreases HMF yield. Therefore, it is essential to limit the diffusion of catalyst into the organic phase, maintain high catalyst concentration in the aqueous phase, and, at the same time, ensure a high organic phase/aqueous phase ratio.…”
Section: Solvents For Hmf Synthesismentioning
confidence: 99%
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“…One alternative solution is to use a biphasic reaction system with a water-immiscible organic phase such as methyl isobutyl ketone, methyl tetrahydrofuran or butanol. [19][20][21] In such systems, the fructose is dehydrated in the aqueous phase by an acid catalyst to produce 5-HMF, which is then extracted into the organic phase, thus avoiding the further degradation of 5-HMF in the aqueous solution, and the resulting 5-HMF is obtained in a yield of up to 75%. 22 The advantage of this process is that the fructose concentration in the aqueous phase can be very high, which facilitates a higher space-time yield of the reaction.…”
Section: Introductionmentioning
confidence: 99%