http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Yu, Iris K.M.,Tsang, Daniel C.W.,Chen, Season S.,Wang, Lei,Hunt, Andrew J.,Sherwood, James,De Oliveira Vigier, Karine,Jé,rô,me, Franç,ois,Ok, Yong Sik,Poon, Chi Sun Elsevier 2017 Bioresource technology Vol.245 No.1
<P><B>Abstract</B></P> <P>Valorisation of bread waste for hydroxymethylfurfural (HMF) synthesis was examined in dimethyl sulfoxide (DMSO)-, tetrahydrofuran (THF)-, acetonitrile (ACN)-, and acetone-water (1:1v/v), under heating at 140°C with SnCl<SUB>4</SUB> as the catalyst. The overall rate of the process was the fastest in ACN/H<SUB>2</SUB>O and acetone/H<SUB>2</SUB>O, followed by DMSO/H<SUB>2</SUB>O and THF/H<SUB>2</SUB>O due to the rate-limiting glucose isomerisation. However, the formation of levulinic acid (via rehydration) and humins (via polymerisation) was more significant in ACN/H<SUB>2</SUB>O and acetone/H<SUB>2</SUB>O. The constant HMF maxima (26–27mol%) in ACN/H<SUB>2</SUB>O, acetone/H<SUB>2</SUB>O, and DMSO/H<SUB>2</SUB>O indicated that the rates of desirable reactions (starch hydrolysis, glucose isomerisation, and fructose dehydration) relative to undesirable pathways (HMF rehydration and polymerisation) were comparable among these mediums. They also demonstrated higher selectivity towards HMF production over the side reactions than THF/H<SUB>2</SUB>O. This study differentiated the effects of polar aprotic solvent-water mediums on simultaneous pathways during biomass conversion.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Bread waste was valorised for the synthesis of HMF, with yields of 26–27mol%. </LI> <LI> Fastest HMF production took place in ACN/H<SUB>2</SUB>O and acetonitrile/H<SUB>2</SUB>O systems. </LI> <LI> Slow glucose isomerization hindered HMF formation in DMSO/H<SUB>2</SUB>O and THF/H<SUB>2</SUB>O. </LI> <LI> Similar HMF selectivity was achieved in ACN/H<SUB>2</SUB>O, acetonitrile/H<SUB>2</SUB>O, and DMSO/H<SUB>2</SUB>O. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>