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Characterizing the chemistry of artificially degraded Scots pine wood serving as a model of naturally degraded waterlogged wood using1H–13C HSQC NMR
AbstractChemically and biologically degraded Scots pine wood was prepared as a model material for the research on new conservation agents for waterlogged archeological wood. In this study, the model wood was characterized using a 2D1H–13C solution-state NMR technique without derivatization, isolation, or extraction to assess the effect of applied degradation processes on its chemical composition and structure. The results clearly show how the two artificially degraded model wood types are chemically different. Biological decay by the brown-rot fungus Coniophora puteana caused degradation of wood polysaccharides, with heavy depletion in arabinan, mannan, and galactan, along with an increase in the cellulose's reducing ends (i.e., lowering the degree of polymerization) and partial deacetylation of mannan. The fungus cleaved roughly one-fifth of the β-aryl ethers in lignin, leading to a broadening effect on the lignin aromatic unit contours; other lignin sidechains were left untouched. Chemical degradation by NaOH hydrolysis resulted in a depletion in mannan, galactan, and glucan, as well as efficient deacetylation of mannan. It also decreased lignin content, causing changes in its structure; minor β-aryl ether cleavage along with substantial phenylcoumaran cleavage were evident. Detailed knowledge about the chemical composition and structure of artificially degraded model pine wood obtained in this research is necessary to understand the reactivity of these wood types with chemicals used for their conservation. This research will help explain the differences in the stabilization effectiveness observed between these wood types treated during conservation and understand the stabilization mechanisms, thus contributing to developing new, more effective conservation agents for wooden artifacts of Cultural Heritage.
Bioethanol Production from Lignocellulosic Biomass—Challenges and Solutions
Regarding the limited resources for fossil fuels and increasing global energy demands, greenhouse gas emissions, and climate change, there is a need to find alternative energy sources that are sustainable, environmentally friendly, renewable, and economically viable. In the last several decades, interest in second-generation bioethanol production from non-food lignocellulosic biomass in the form of organic residues rapidly increased because of its abundance, renewability, and low cost. Bioethanol production fits into the strategy of a circular economy and zero waste plans, and using ethanol as an alternative fuel gives the world economy a chance to become independent of the petrochemical industry, providing energy security and environmental safety. However, the conversion of biomass into ethanol is a challenging and multi-stage process because of the variation in the biochemical composition of biomass and the recalcitrance of lignin, the aromatic component of lignocellulose. Therefore, the commercial production of cellulosic ethanol has not yet become well-received commercially, being hampered by high research and production costs, and substantial effort is needed to make it more widespread and profitable. This review summarises the state of the art in bioethanol production from lignocellulosic biomass, highlights the most challenging steps of the process, including pretreatment stages required to fragment biomass components and further enzymatic hydrolysis and fermentation, presents the most recent technological advances to overcome the challenges and high costs, and discusses future perspectives of second-generation biorefineries.
Reactivity of Waterlogged Archeological Elm Wood with Organosilicon Compounds Applied as Wood Consolidants: 2D 1H–13C Solution-State NMR Studies
Some organosilicon compounds, including alkoxysilanes and siloxanes, proved effective in stabilizing the dimensions of waterlogged archaeological wood during drying, which is essential in the conservation process of ancient artifacts. However, it was difficult to determine a strong correlation between the wood stabilizing effect and the properties of organosilicon compounds, such as molecular weight and size, weight percent gain, and the presence of other potentially reactive groups. Therefore, to better understand the mechanism behind the stabilization effectiveness, the reactivity of organosilicons with wood polymers was studied using a 2D 1H–13C solution-state NMR technique. The results showed an extensive modification of lignin through its demethoxylation and decarbonylation and also the absence of the native cellulose anomeric peak in siloxane-treated wood. The most substantial reactivity between wood polymers and organosilicon was observed with the (3-mercaptopropyl)trimethoxysilane treatment, showing complete removal of lignin side chains, the lowest syringyl/guaiacyl ratio, depolymerization of cellulose and xylan, and reactivity with the C6 primary hydroxyls in cellulose. This may explain the outstanding stabilizing effectiveness of this silane and supports the conclusion that extensive chemical interactions are essential in this process. It also indicates the vital role of a mercapto group in wood stabilization by organosilicons. This 2D NMR technique sheds new light on the chemical mechanisms involved in organosilicon consolidation of wood and reveals what chemical characteristics are essential in developing future conservation treatments.