Search

Defect-free, highly-densified panels without springback were prepared from Hyun aspen (Populus alba × glandulosa) wood with different delignification levels by alkaline hydrogen peroxide (AHP) pretreatment. The AHP concentrations were adjusted to 3%, 7%, 10%, while the temperature (100 °C), time (3 h), pH (11), liquor ratio (6.25), and stabilizer (0.5% EDTA) remained constant. The delignification of Hyun aspen wood panels was indirectly quantified by analyzing the UV absorbance of the spent liquor after AHP treatment, wherein delignification ranged from 12% to 58% depending on the AHP concentration. To achieve highly-densified panels, the densification conditions, such as pressure, temperature, and time, were examined. Panels subjected to cold-pressing (25 °C) at 30 MPa for 1 h, followed by hot-pressing (105 °C) at 30 MPa for 6 h, then immediately removed after heating, resulted in durable, highly-densified panels with no springback or cracks.

The study’s goal was to investigate the delignification characteristics using alkaline hydrogen peroxide (AHP) under atmospheric pressure, intending it as a pre-treatment method for transforming low-value lignocellulosic biomass into high-performance structural materials. The lignocellulosic biomass used in this study were Japanese cedar (Cryptomeria japonica), Hyun aspen (Populus alba x glandulosa), and bamboo (Phyllostachys pubescens), which are underutilized and low-value lignocellulosic biomass in Korea. The delignification conditions used were pH 11, liquor ratio 12.5, H2O2 (3 to 10%), temperature (25 to 100 °C), and time (1 to 24 h). Japanese cedar exhibited

The dyeing characteristics of hardwood kraft lignin (KL) were investigated on cotton fabrics, assessing its potential as a sustainable and environmentally friendly dye. Dyeability was evaluated by varying the KL concentrations, temperature, and time. An aqueous solution of Na2CO3 (1.0%) as the dye bath and a fabric-to-liquor ratio of 1:50 were used. Cationizing effects were studied using (3-chloro-2-hydroxypropyl) trimethylammonium chloride (CHPTAC), and the mordanting effects of various mordants were also evaluated. Post-mordanting was performed with FeSO4, FeCl2, Fe-lactate (Fe-lac), MgSO4, CuCl2, CuSO4, and Al2(SO4)3. A mordant concentration of 1 mM o.w.f. (0.5 mM for Al2(SO4)3), with a liquor ratio of 1:30, at 60 °C for 30 min were employed. Suitable dyeing conditions were 2.0% o.w.b., 90 °C, and 90 min, resulting in a brownish color of the cotton fabric. The fabrics exhibited a range of light brown to light grayish brown colors and showed lighter colors than the untreated fabrics when mordanted with MgSO4 and Al2(SO4)3. The color difference (ΔE) between cationized and uncationized cotton fabrics was 3.48. From the colorfastness assessment, KL-dyed cotton fabric showed good rubbing and washing fastness for staining, but poor light and washing fastness for fading.

Thermal characterization of kraft lignin (KL) prepared from mixed hardwoods was conducted to determine their thermal and thermo-oxidative stability, glass transition temperature (Tg), pyrolysis products composition, and syringyl/guaiacyl ratio. Two milled wood lignins (MWLs) from acacia (MWL-aca) and mixed hardwoods (MWL-mhw), the same hardwood species employed in the production of KL, were also characterized for comparison with KL. Thermogravimetric analysis (TGA) indicated that KL had higher thermal and thermo-oxidative stability than MWLs. Based on differential scanning calorimetry (DSC), the Tg of KL was 63.2 °C, while MWLs gave similar values near 165 °C. The syringyl (S), guaiacyl (G), p-hydroxyphenyl (H) composition of KL acquired from pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) at 675 °C was 48:44:8 (S/G ratio 1.07), while MWL-aca and MWL-mhw were 31:60:9 and 46:48:6, respectively.

This study was conducted to determine the lignin substructures, hydroxyl (phenolic + aliphatic) contents, and carboxyl contents in kraft lignin (KL) prepared from mixed hardwoods by using 2D Heteronuclear Multiple Quantum Coherence Nuclear Magnetic Resonance (HMQC NMR) and 31P NMR techniques. Based on 2D HMQC NMR analysis of KL, stilbene and vanillin substructures were present in the aromatic region, while trace amounts of β-O-4 and β-β moieties were detected in the oxygenated aliphatic region. The total hydroxyl content calculated from 31P NMR was 5.24 mmol/g KL. The aliphatic hydroxyl content was 1.04 mmol/g KL, and phenolic hydroxyl content was 4.20 mmol/g KL. Of the phenolic hydroxyl groups, the contribution of syringyl (S) and guaiacyl (G) was 1.02 and 0.97 mmol/g KL, respectively. The S/G molar ratio of KL calculated from 31P NMR was 1.05. The carboxyl content was 0.44 mmol/g KL.

The study's goal was to investigate the delignification characteristics using alkaline hydrogen peroxide (AHP) under atmospheric pressure, intending it as a pre-treatment method for transforming low-value lignocellulosic biomass into high-performance structural materials. The lignocellulosic biomass used in this study were Japanese cedar (Cryptomeria japonica), Hyun aspen (Populus alba x glandulosa), and bamboo (Phyllostachys pubescens), which are underutilized and low-value lignocellulosic biomass in Korea. The delignification conditions used were pH 11, liquor ratio 12.5, H2O2 (3 to 10%), temperature (25 to 100 °C), and time (1 to 24 h). Japanese cedar exhibited <30% delignification even under the most severe conditions. In contrast, Hyun aspen achieved more than double that level of delignification. However, reaching over 60% delignification was challenging. Bamboo was easily delignified, reaching approximately 80% delignification using similar conditions performed in Japanese cedar and Hyun aspen. These differences observed in AHP delignification among three species were likely to be primarily due to the structural differences and proportion of condensed units in lignin. Consequently, for Hyun aspen and bamboo, the AHP delignification process under atmospheric pressure was considered to be feasible as a pre-treatment method for high-performance structural materials. [ABSTRACT FROM AUTHOR]

The dyeing characteristics of hardwood kraft lignin (KL) were investigated on cotton fabrics, assessing its potential as a sustainable and environmentally friendly dye. Dyeability was evaluated by varying the KL concentrations, temperature, and time. An aqueous solution of Na2CO3 (1.0%) as the dye bath and a fabric-to-liquor ratio of 1:50 were used. Cationizing effects were studied using (3-chloro-2-hydroxypropyl) trimethylammonium chloride (CHPTAC), and the mordanting effects of various mordants were also evaluated. Post-mordanting was performed with FeSO4, FeCl2, Fe-lactate (Fe-lac), MgSO4, CuCl2, CuSO4, and Al2(SO4)3. A mordant concentration of 1 mM o.w.f. (0.5 mM for Al2(SO4)3), with a liquor ratio of 1:30, at 60 °C for 30 min were employed. Suitable dyeing conditions were 2.0% o.w.b., 90 °C, and 90 min, resulting in a brownish color of the cotton fabric. The fabrics exhibited a range of light brown to light grayish brown colors and showed lighter colors than the untreated fabrics when mordanted with MgSO4 and Al2(SO4)3. The color difference (E) between cationized and uncationized cotton fabrics was 3.48. From the colorfastness assessment, KL-dyed cotton fabric showed good rubbing and washing fastness for staining, but poor light and washing fastness for fading. [ABSTRACT FROM AUTHOR]

Thermal characterization of kraft lignin (KL) prepared from mixed hardwoods was conducted to determine their thermal and thermooxidative stability, glass transition temperature (Tg), pyrolysis products composition, and syringyl/guaiacyl ratio. Two milled wood lignins (MWLs) from acacia (MWL-aca) and mixed hardwoods (MWL-mhw), the same hardwood species employed in the production of KL, were also characterized for comparison with KL. Thermogravimetric analysis (TGA) indicated that KL had higher thermal and thermo-oxidative stability than MWLs. Based on differential scanning calorimetry (DSC), the Tg of KL was 63.2 °C, while MWLs gave similar values near 165 °C. The syringyl (S), guaiacyl (G), p-hydroxyphenyl (H) composition of KL acquired from pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) at 675 °C was 48:44:8 (S/G ratio 1.07), while MWL-aca and MWL-mhw were 31:60:9 and 46:48:6, respectively. [ABSTRACT FROM AUTHOR]

This study was conducted to determine the lignin substructures, hydroxyl (phenolic + aliphatic) contents, and carboxyl contents in kraft lignin (KL) prepared from mixed hardwoods by using 2D Heteronuclear Multiple Quantum Coherence Nuclear Magnetic Resonance (HMQC NMR) and 31P NMR techniques. Based on 2D HMQC NMR analysis of KL, stilbene and vanillin substructures were present in the aromatic region, while trace amounts of β-O-4 and β-β moieties were detected in the oxygenated aliphatic region. The total hydroxyl content calculated from 31P NMR was 5.24 mmol/g KL. The aliphatic hydroxyl content was 1.04 mmol/g KL, and phenolic hydroxyl content was 4.20 mmol/g KL. Of the phenolic hydroxyl groups, the contribution of syringyl (S) and guaiacyl (G) was 1.02 and 0.97 mmol/g KL, respectively. The S/G molar ratio of KL calculated from 31P NMR was 1.05. The carboxyl content was 0.44 mmol/g KL. [ABSTRACT FROM AUTHOR]

The structural and thermal characterization of milled wood lignin (MWL) prepared from bamboo (Phyllostachys pubescens) grown in Korea was investigated, and the results were compared with bamboo MWLs from other studies. The C9 formula of the bamboo MWL was C9H7.76O3.23N0.02 (OCH3)1.41. The Mw and Mn of MWL were 13,000 and 4400 Da, respectively, which resulted in a polydispersity index (PDI) of 3.0. The PDI of the prepared MWL was higher than other bamboo MWLs (1.3–2.2), suggesting a broader molecular weight distribution. The structural features of MWL were elucidated using FT-IR spectroscopy and NMR techniques (1H, 13C, HSQC, 31P NMR), which indicate that MWL is of the HGS-type lignin. The major lignin linkages (β-O-4, β-β, β-5) were not different from other bamboo MWLs. The syringyl/guaiacyl ratio, determined from 1H NMR, was calculated as 0.89. 31P NMR revealed variations in hydroxyl content, with a higher aliphatic hydroxyl content in MWL compared to other bamboo MWLs. Thermal properties were investigated through TGA, DSC, and pyrolysis-GC/MS spectrometry (Py-GC/MS). The DTGmax of MWL under inert conditions was 287 °C, and the Tg of MWL was 159 °C. Py-GC/MS at 675 °C revealed a syringyl, guaiacyl, p-hydroxyphenyl composition of 17:37:47.

Chemical characterization of kraft lignin (KL) from mixed hardwoods (Acacia spp. from Vietnam and mixed hardwoods (mainly Quercus spp.) from Korea) was conducted for its future applications. To compare the structural changes that occurred in KL, two milled wood lignins (MWLs) were prepared from the same hardwood samples used in the production of KL. Elemental analysis showed that the MWL from acacia (MWL-aca) and mixed hardwood (MWL-mhw) had almost similar carbon content, methoxyl content, and C9 formula. KL had high carbon content but low oxygen and methoxyl contents compared to MWLs. The C9 formula of KL was determined to be C9H7.29O2.26N0.07S0.12(OCH3)1.24. The Mw of KL and MWLs was about 3000 Da and 12,000–13,000 Da, respectively. The structural features of KL and MWLs were investigated by Fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance spectrometry (1H, 13C NMR). The analyses indicated that KL underwent severe structural modifications, such as γ-carbon cleavage, demethylation, and polycondensation reactions during kraft pulping, which resulted in increased aromatic content and decreased aliphatic content. The main linkages in lignin, β-O-4 moieties, were hardly detected in the analysis as these linkages were extensively cleaved by nucleophilic attack of SH- and OH- during pulping.