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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.

This preliminary study aimed to realize the potential use of titanium dioxide–carbonized medium-density fiberboard (TiO2–cMDF) as a biomaterial for dye wastewater treatment. TiO2–cMDF, which was prepared by carbonizing MDF treated with titanium tetraisopropoxide in isopropyl alcohol, was investigated for adsorption and then photodegradation of methylene blue (MB) under UV-A (390 nm, 19 W) and UV-C (280 nm, 12 W) light emitting diodes (LEDs). After two full cycles of adsorption, four successive cycles of photodegradation were conducted under UV-A LED. For every adsorption or photodegradation cycle, TiO2–cMDF practically removed MB. Both adsorption and photodegradation followed pseudo-first-order kinetics. The rate constants for adsorption decreased by half. The rate constants for photodegradation were similar. This finding suggests that UV-A LED is a robust and steady source of UV light. Photodegradation under UV-C LED was also performed. However, due to its high-energy output, the UV-C LED module overheated even though a cooling fan was present. Although the results indicate a slow photodegradation under UV LEDs, because of the limited number of specimens, increasing the number of specimens and UV LED modules will improve its performance.

A solution-type TiO2-based photocatalyst for the decomposition of volatile organic compounds was synthesized using a modified sol-gel method under either alcohol (ethanol or isopropanol) or aqueous conditions. Anatase-type TiO2 was successfully synthesized with additional hydrothermal treatment using either type of medium. However, the aqueous condition for TiO2 synthesis was more convenient for the formation of anatase-type TiO2. Based on X-ray diffraction analysis data, the optimal hydrothermal treatment temperature was 80 °C for anatase-type TiO2 formation; at temperatures below 80 °C or above 90 °C, mostly rutile-type TiO2 was formed. The synthesized anatase-type TiO2 solution was applied to the surface of carbonized medium-density fiberboard (c-MDF). The anatase-type TiO2 on c-MDF showed good maintenance of toluene decomposition performance even after repeated use for 14 weeks.

Photocatalytic carbonized medium density fiberboard (MDF) was prepared by one-step carbonization with titanium tetraisopropoxide (Ti-tip) as a TiO2 precursor. Anatase TiO2 was formed at carbonizing temperatures of 600 to 800 °C. However, at > 900 °C, most crystalline TiO2 was rutile. Ti-tip-treated carbonized MDF (c-MDF) showed outstanding formaldehyde reduction performance with complete removal of formaldehyde from the chamber in 1 to 3 days. However, with non Ti-tip-treated c-MDF, formaldehyde remained after 20 days. No toluene was detected after 3 h on 50% Ti-tip-treated c-MDF, while toluene was continuously detected with other samples (10% and 5% Ti-tip-treated c-MDF, and untreated c-MDF). After 9 h ultraviolet exposure, toluene was completely reduced on 10% and 50% Ti-tip-treated c-MDF; reduction was only 20% on untreated c-MDF. In addition, c-MDF/TiO2 prepared at 800 and 900 °C had significantly higher photocatalytic performances compared to those obtained at lower carbonization temperatures. Based on the results, the combination of 10% Ti-tip treatment and carbonizing at 800 °C provided the optimum photodegradation capacity for formaldehyde and toluene.