2016
DOI: 10.15376/biores.12.1.344-361
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The Critical Analysis of Catalytic Steam Explosion Pretreatment of Corn Stalk, Lignin Degradation, Recovery, and Characteristic Variations

Abstract: The lignin degradation and its structural change as a result of catalytic steam explosion pretreatment can be considered of great importance for both the subsequent fermentation and the further utilization of the lignin fraction. This work investigated the degradation mechanism and change in the characteristics of lignin during dilute sulphuric-acid catalytic steam explosion (SE) pretreatment and ammonia catalytic steam explosion (AE) pretreatment of corn stalk. For this purpose, two types of lignin samples ob… Show more

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Cited by 7 publications
(6 citation statements)
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“…73 In addition, C 9 H 10 O 3 (#61) and C 12 H 16 O 4 (#63), two phenolic compounds with relatively lower O/C ratios, have been detected in lignin degradation products related to various decomposition processes such as thermal pyrolysis, 53,74 biodegradation, 75 and catalytic treatment. 76 The second group of CHO species identified as "f lavonoids" shows higher carbon numbers and O/C ratios than the phenolic/lignin-derived compounds (mean: 19 ± 4 and 0.45 ± 0.09, respectively; Table 1). These chromophores have two distinctive UV−vis absorption bands at wavelengths of 250− 270 nm and 330−350 nm (Figure 3c,d).…”
Section: ■ Results and Discussionmentioning
confidence: 99%
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“…73 In addition, C 9 H 10 O 3 (#61) and C 12 H 16 O 4 (#63), two phenolic compounds with relatively lower O/C ratios, have been detected in lignin degradation products related to various decomposition processes such as thermal pyrolysis, 53,74 biodegradation, 75 and catalytic treatment. 76 The second group of CHO species identified as "f lavonoids" shows higher carbon numbers and O/C ratios than the phenolic/lignin-derived compounds (mean: 19 ± 4 and 0.45 ± 0.09, respectively; Table 1). These chromophores have two distinctive UV−vis absorption bands at wavelengths of 250− 270 nm and 330−350 nm (Figure 3c,d).…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…C 9 H 8 O 6 is probably carboxyvanillic acid from biodegradation of biphenyl lignin compounds by soil bacterials . In addition, C 9 H 10 O 3 (#61) and C 12 H 16 O 4 (#63), two phenolic compounds with relatively lower O/C ratios, have been detected in lignin degradation products related to various decomposition processes such as thermal pyrolysis, , biodegradation, and catalytic treatment …”
Section: Resultsmentioning
confidence: 99%
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“…Careful examination of lignin fractions from the solvent fraction process revealed a significant difference in the absorption at 1699 cm −1 , corresponding to conjugated ester linkage stretching, which was attributed to the ester bond of the phenolic acids to lignin [17]. This result indicated that the low-molecular-weight lignin fraction contained excess phenolic acids than the high-molecular-weight lignin fraction [18]. FT-IR is a useful approach for studying various functional groups as well as the conformational properties of lignin.…”
Section: Ft-irmentioning
confidence: 97%
“…The above-mentioned structural characteristics were explained by the fact that the SE-NaOH-pretreated CS had a high accessibility and low enzyme adsorption rate after enzymatic hydrolysis. This could have been because of the role that chemical high-temperature cooking plays in the degradation of hemicellulose and lignin, as well as the softening and exposing of cellulose (Yang et al 2017).…”
Section: Sem Analysismentioning
confidence: 99%