Dehydration Reaction of Fructose to 5-Hydroxymethylfurfural over Various Keggin-type Heteropolyacids 


Vol. 16,  No. 3, pp. 220-228, Sep.  2010


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  Abstract

Four Keggin-type heteropolyacids, HnXM12O40(X = P and Si, M = W and Mo) that were substituted with heteroatom and polyatom were applied to the dehydration reaction of fructose to 5-hydroxymethylfurfural(HMF). The results showed that the acid became stronger when the heteroatom and polyatom were substituted with P and W than the cases of Si and Mo, respectively. However, the amount of acidic sites increased with the decrease in the acid strength, resulting in the change of the catalytic activity of heteropolyacids in the dehydration reaction. The experimental results revealed that four different heteropolyacids produced similar amounts of HMF via the dehydration reaction of fructose due to the counterbalancing effect between the amount of active sites, which is related to the catalytic activityof heteropolyacids, and the softness of polyanion. In addition, it was observed that the prepared heteropolyacids showed good structural stability after heat treatment at 200℃.

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  Cite this article

[IEEE Style]

B. J, Y. HJ, K. ND, C. Y, Y. J, "Dehydration Reaction of Fructose to 5-Hydroxymethylfurfural over Various Keggin-type Heteropolyacids," Clean Technology, vol. 16, no. 3, pp. 220-228, 2010. DOI: .

[ACM Style]

Baek J, Yun HJ, Kim ND, Choi Y, and Yi J. 2010. Dehydration Reaction of Fructose to 5-Hydroxymethylfurfural over Various Keggin-type Heteropolyacids. Clean Technology, 16, 3, (2010), 220-228. DOI: .

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