Fractionating pretreatment of sugarcane bagasse by aqueous formic acid with direct recycle of spent liquor to increase cellulose digestibility–the Formiline process

2012 ◽  
Vol 117 ◽  
pp. 25-32 ◽  
Author(s):  
Xuebing Zhao ◽  
Dehua Liu
Molecules ◽  
2021 ◽  
Vol 26 (9) ◽  
pp. 2753
Author(s):  
Xiaogang Chang ◽  
Jingzhi Zhang ◽  
Ruchun Wu ◽  
Xuebing Zhao

In order to more conveniently simulate and optimize the solubilization of sugarcane bagasse components during formic acid (FA) fractionation, an extended combined severity factor (CSFext) was defined to integrate various operation parameters as a single factor. Two phenomenological models based on Arrhenius and Logistic equations were further used to describe the phenomenological kinetics. Different data-processing methods were compared to fit the severity parameters and model constants. Both Arrhenius-based and Logistic-based models show satisfying fitting results, though the values of Arrhenius-based CSFext (A-CSFext) and Logistic-based CSFext (L-CSFext) were somewhat different under the same fractionation condition. The solubilization of biomass components increased with CSFext, but two distinct stages could be observed with inflection points at A-CSFext of 42 or L-CSFext of 43, corresponding to bulk and residual solubilization stages, respectively. For the enzymatic hydrolysis of cellulosic solids, the highest initial enzymatic glucan conversion (EGC@6h) was obtained at A-CSFext of 39–40 or A-CSFext of 40–41; however, for a long hydrolysis period (72 h), relatively high glucan conversion (EGC@72h) was observed at A-CSFext of 42–43 or A-CSFext of 43–44. Post-treatment for deformylation with a small amount of lime could help to recover the cellulose digestibility.


ChemInform ◽  
2005 ◽  
Vol 36 (15) ◽  
Author(s):  
Shinya Nomoto ◽  
Daisuke Yoshimura ◽  
Masayosi Hagiwara ◽  
Masaki Kozono ◽  
Masanori Terasaki ◽  
...  

2020 ◽  
Vol 10 (5) ◽  
pp. 1713 ◽  
Author(s):  
Chang-Seob Seo ◽  
Hyeun-Kyoo Shin

Yeonkyopaedok-san is a traditional Korean medicine used in the early treatment of boils. In the present study, its 12 marker components for quality control were determined using high-performance liquid chromatography (HPLC) with photodiode array detection and ultra-performance liquid chromatography–mass spectrometry with tandem mass spectrometry (UPLC–MS/MS). The investigated 12 marker components of Yeonkyopaedok-san were as follows: 3-caffeoylquinic acid, cimifugin 7-glucoside, liquiritin apioside, ferulic acid, narirutin, 5-O-methylvisammioside, naringin, neohesperidin, oxypeucedanin hydrate, arctigenin, glycyrrhizic acid, and 6-gingerol. The analytical column used for the separation of the 12 marker analytes in Yeonkyopaedok-san was a Waters SunFire C18 column (4.6 mm × 250 mm, 5 μm). The two mobile phases used were 0.1% (v/v) aqueous formic acid and 0.1% (v/v) formic acid in acetonitrile. In the UPLC–MS/MS analysis, all components were separated using a Waters ACQUITY UPLC BEH C18 column (2.1 mm × 100 mm, 1.7 μm). The two mobile phases used were 0.1% (v/v) aqueous formic acid and acetonitrile. The coefficient of determination of the calibration curves in both analysis systems showed good linearity (>0.99). The amounts of the 12 marker components in Yeonkyopaedok-san determined using HPLC–photodiode array detection and UPLC–MS/MS analyses were found to be 0.14–9.00 mg/g and 2.35–853.11 μg/g, respectively.


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