We investigated the interactive effects of elevated concentrations of carbon dioxide ([CO(2)]) and ozone ([O(3)]) on radial growth, wood chemistry and structure of five 5-year-old trembling aspen (Populus tremuloides Michx.) clones and the wood chemistry of paper birch (Betula papyrifera Marsh.). Material for the study was collected from the Aspen FACE (free-air CO(2) enrichment) experiment in Rhinelander, WI, where the saplings had been exposed to four treatments: control, elevated [CO(2)] (560 ppm), elevated [O(3)] (1.5 x ambient) and their combination for five growing seasons. Wood properties of both species were altered in response to exposure to the treatments. In aspen, elevated [CO(2)] decreased uronic acids (constituents of, e.g., hemicellulose) and tended to increase stem diameter. In response to elevated [O(3)] exposure, acid-soluble lignin concentration decreased and vessel lumen diameter tended to decrease. Elevated [O(3)] increased the concentration of acetone-soluble extractives in paper birch, but tended to decrease the concentration of these compounds in aspen. In paper birch, elevated [CO(2)] decreased and elevated [O(3)] increased starch concentration. The responses of wood properties to 5 years of fumigation differed from those previously reported after 3 years of fumigation.
Sodium sulphite pulping of Scots pine chips in the initial pH range of 7.5–9 was investigated at 180°C and 165°C (for 120–240 min), using chemical charges between 25 and 50% and anthraquinone (AQ) charges 0–0.2%. As a result, pulps with yields of 52–73% and kappa numbers of 35–106 were produced. Delignification was accelerated by higher Na2SO3 charges and temperatures, and by AQ addition, whereas the effect of initial pH was negligible. The high pulp yields at a given kappa number were attributable to high retention of hemicelluloses, especially that of galactoglucomannan. The relatively low viscosities of pulps were apparently caused by depolymerisation of cellulose by sulphite. The sulphonic acid groups in the pulps correlated well with the residual lignin content, although some sulphonation of polysaccharides may also be possible. The results indicate that pulping of softwood in buffer-free (without Na2CO3 and/or NaOH) sodium sulphite liquor may result in pulps with tailored characteristics.
Ultraviolet resonance Raman (UVRR) spectroscopy is a powerful tool for structural lignin analysis in situ: modification or isolation of lignin from biomass is not necessary. UVRR spectroscopy is equally applicable for samples with high lignin content and those with very low lignin content. Monomeric phenolic lignin model compounds and wood pulp samples have been studied at neutral and alkaline pH with UVRR spectroscopy. Concentration of guaiacol correlated well with the relative Raman band intensity, which indicates that lignin-containing solutions can be quantitatively measured with UVRR spectroscopy. A change in pH induced a recordable shift in the aromatic band position in the spectra, which was 25–35 cm-1 with phenolic model compounds without para substitution, 8–12 cm-1 with phenolic model compounds with para substitution, and about 2–7 cm-1 with pulp samples. No shift was detected with a non-phenolic model compound. Increasing the amount of phenolic hydroxyl groups increased the UVRR band shift in pulp samples. Additionally, increasing the pH enhanced the relative aromatic band intensity in the UVRR spectra in solution of the phenolic model compound. Accordingly, pH adjustment is relevant prior to any lignin analysis with Raman spectroscopy.
Birch and eucalyptus kraft pulps were treated with sulfite solutions in neutral conditions (pH 7) at 170 °C for 60 min and at 190 °C for 180 min. The pulps were analyzed for kappa number, viscosity, carbohydrate composition, and optical properties. Additionally, UV resonance Raman (UVRR) spectroscopy was applied to collect information on the contents of hexenuronic acid (HexA), lignin, and its phenolic hydroxyl groups. The sulfite treatments resulted in (i) depolymerization and partial dissolution of cellulose, (ii) partial dissolution of xylan and substantial decrease in its HexA content, and (iii) removal of the major part of lignin and increase in its phenolic hydroxyl group content. The extensive removal of HexA and depolymerization of cellulose by neutral sulfite were unexpected phenomena that have not been previously reported. According to their degree of polymerization (DP), the pulps were mainly in the form of microcrystalline cellulose after the more drastic treatments.
Lignin α-carbonyl groups play an important role in light-induced yellowing as initial absorber of UV light. The model compounds vanillin, verataldehyde, and acetovanillone were studied and the reaction rate coefficient k was calculated for the addition of bisulphite to carbonyls. UV-Vis spectra of the model compounds in bisulphite solution were measured between 200 and 400 nm and at a single wavelength of 305 nm. The reaction was fastest with vanillin, but only a minor part of acetovanillone reacted, which can be explained with different reactivity of aldehydes and ketones. Calculated reaction rate coefficients were 26×10-3 s-1 and 18×10-3 s-1 for vanillin and verataldehyde, respectively. Sheets from chemi-thermomechanical pulp (CTMP) were treated with bisulphite solutions (10 mM, 20 mM and 0.1 M; for 1 and 5 min) in order to study the potential of this treatment in retarding yellowing of CTMP. Initial brightness was improved with the treatments, but as the brightness loss was even more drastic, stabilization was not achieved. FT-IR spectra of bisulphite treated samples revealed that only part of the carbonyl groups reacted. The unsuccessful light stabilization of the pulp originated probably from an inadequate carbonyl addition, a problem which could not be resolved.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.