A technical and economic analysis of acid-catalyzed steam explosion and dilute sulfuric acid pretreatments using wheat straw or aspen wood chips

1991 ◽  
Vol 28-29 (1) ◽  
pp. 87-97 ◽  
Author(s):  
D. J. Schell ◽  
R. Torget ◽  
A. Power ◽  
P. J. Walter ◽  
K. Grohmann ◽  
...  
Agronomy ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 487
Author(s):  
Dimitrios Ilanidis ◽  
Stefan Stagge ◽  
Leif J. Jönsson ◽  
Carlos Martín

Biochemical conversion of wheat straw was investigated using hydrothermal pretreatment, enzymatic saccharification, and microbial fermentation. Pretreatment conditions that were compared included autocatalyzed hydrothermal pretreatment at 160, 175, 190, and 205 °C and sulfuric-acid-catalyzed hydrothermal pretreatment at 160 and 190 °C. The effects of using different pretreatment conditions were investigated with regard to (i) chemical composition and enzymatic digestibility of pretreated solids, (ii) carbohydrate composition of pretreatment liquids, (iii) inhibitory byproducts in pretreatment liquids, (iv) furfural in condensates, and (v) fermentability using yeast. The methods used included two-step analytical acid hydrolysis combined with high-performance anion-exchange chromatography (HPAEC), HPLC, ultra-high performance liquid chromatography-electrospray ionization-triple quadrupole-mass spectrometry (UHPLC-ESI-QqQ-MS), and pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS). Lignin recoveries in the range of 108–119% for autocatalyzed hydrothermal pretreatment at 205 °C and sulfuric-acid-catalyzed hydrothermal pretreatment were attributed to pseudolignin formation. Xylose concentration in the pretreatment liquid increased with temperature up to 190 °C and then decreased. Enzymatic digestibility was correlated with the removal of hemicelluloses, which was almost quantitative for the autocatalyzed hydrothermal pretreatment at 205 °C. Except for the pretreatment liquid from the autocatalyzed hydrothermal pretreatment at 205 °C, the inhibitory effects on Saccharomyces cerevisiae yeast were low. The highest combined yield of glucose and xylose was achieved for autocatalyzed hydrothermal pretreatment at 190 °C and the subsequent enzymatic saccharification that resulted in approximately 480 kg/ton (dry weight) raw wheat straw.


2011 ◽  
Vol 102 (10) ◽  
pp. 6134-6140 ◽  
Author(s):  
Xiaochen Yu ◽  
Yubin Zheng ◽  
Kathleen M. Dorgan ◽  
Shulin Chen

2015 ◽  
Vol 129 ◽  
pp. 79-86 ◽  
Author(s):  
Qian-Qian Wu ◽  
Yu-Long Ma ◽  
Xuan Chang ◽  
Yong-Gang Sun

2012 ◽  
Vol 472-475 ◽  
pp. 2828-2833
Author(s):  
Yan Qiao Jin ◽  
Yi Zhuan Zhang ◽  
Xian Su Cheng

In this study, wheat-straw lignocelluloses were liquefied in liquefaction solvents. Polyethyleneglycol 400 (PEG 400) and ethylene glycol (EG) were used as main liquefaction solvents. The effect of liquefaction time and liquefaction solvents on the properties of liquefied products was investigated. As the reaction time increased, the hydroxyl value, residue content and viscosity decreased, and the acid value decreased gradually in the previous period of time then increased. The optimum liquefaction conditions were as follows: wheat-straw lignocelluloses with steam-explosion pretreatment, the main liquefaction reagent of PEG 400, auxiliary liquefaction solvents of glycerin, catalyst of sulfuric acid, liquefaction temperature of 150°C, liquefaction time of 4 h. The hydroxyl value of liquefaction product was 206 mgKOH/g, the residue content was 0.19% and the viscosity was 88 mPa•s.


1984 ◽  
Vol 49 (7) ◽  
pp. 1722-1730 ◽  
Author(s):  
Vojtěch Kmoníček ◽  
Václav Bártl ◽  
Miroslav Protiva

A reaction of 2-(bromomethyl)thioxanthone with sodium methanethiolate with sodium methanethiolate gave 2-(methylthiomethyl)thioxanthone (II) which was transformed by treatment with 3-dimethylaminopropylmagnesium chloride to the tertiary alcohol IV. Its dehydration by heating with dilute sulfuric acid afforded the title compound I. An attempt at preparing the analogous 2-(methoxymethyl) derivative proceeded similarly but failed in the stage of the acid-catalyzed dehydration of the tertiary alcohol V. Acids VIII-XII and the nitrile XIII were prepared as potential intermediates. Compound I has properties of a tranquilizer with a weak cataleptic activity.


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