14 research outputs found

    Two-Step Hydrolysis of Japanese Cedar as Treated by Semi-Flow Hot-Compressed Water with Acetic Acid

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    Hydrothermal decomposition of various crystalline celluloses as treated by semi-flow hot-compressed water

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    Various types of crystalline celluloses I, II, IIII, IIIII, IVI and IVII that have been adjusted for their degree of polymerization were treated by semi-flow hot-compressed water (HCW) at 230–270 °C/10 MPa/15 min to study their hydrothermal decomposition. The treatments resulted in either partial or complete decomposition of the celluloses and the decomposed products were primarily recovered as hydrolyzed, dehydrated and fragmented ones as well as organic acids in the water-soluble (WS) portions. Their results of hydrothermal decomposition and its kinetics revealed that the celluloses decomposition is dependent on the types of crystalline celluloses as well as temperature of the HCW treatment. The outcome from the WS portions at 270 °C/10 MPa/15 min showed that the degree of difficulty for decomposition is lower in group II (cell II, cell IIIII, cell IVII) than group I (cell I, cell IIII, cell IVI), indicating that group II is less resistant to decomposition by HCW treatment. Therefore, the decomposition behaviors of the cellulose are due to the inherent differences in the crystalline structures

    Decomposition behaviors of various crystalline celluloses as treated by semi-flow hot-compressed water

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    Various types of crystalline cellulose consisting of group I (cell I, IIII, IVI) and group II (cell II, IIIII, IVII) prepared from cotton linter were adjusted for their degree of polymerization (DP) as starting materials. These celluloses were then treated by semi-flow hot-compressed water (HCW) at 230–270 °C/10 MPa/2–15 min to study their decomposition behaviors. The treatments performed resulted in residues of celluloses and water-soluble (WS) portions. Consequently, the crystallinity of the residues was found to remain the same, but the DP was reduced as the temperature increased. Additionally, X-ray diffractometry and Fourier transform-infrared analyses demonstrated that crystallographic changes occurred for residues of cell IIII, IVI and IIIII. Despite these changes, the overall results of the residues showed that group I has higher resistance to decomposing than group II. As for the WS portions, the yields of the hydrolyzed and degraded products were higher in group II than group I, indicating that group II is less resistant to decomposition by HCW treatment. Results for both the residues and WS portions are in agreement with each other, showing that the degree of difficulty of decomposition was higher in group I than group II. Therefore, the decomposition behaviors of the celluloses are due to differences in the crystalline forms
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