From liquid to solid-state, solvent-free oxidative ammonolysis of lignins - an easy, alternative approach to generate "N-lignins".

A new chemical modification protocol to generate N-lignins is presented, based on Indulin AT and Mg-lignosulfonate. The already known ammonoxidation reaction in liquid phase was used as a starting point and stepwise optimised towards a full solid-state approach. The "classical" liquid ammonoxidation products, the transition products from the optimization trials, as well as the "solid-state" products were comprehensively analysed and compared to the literature.

A general solvent system for the analysis of lignosulfonates by P NMR.

P nuclear magnetic resonance (NMR) spectroscopy is the most common and most accurate analytical method to quantitatively determine the hydroxy group contents of technical lignins. However, for lignosulfonates, liquid-state NMR analysis is often limited due to solubility problems in commonly used solvent systems, which may arise from the broad range of lignosulfonates from different wood sources, pulping conditions, and purification procedures used in biorefineries. Finding a suitable solvent system is even more difficult for chemically modified or fractionated lignosulfonates.

Intermolecular Interactions in the Membrane Filtration of Highly Alkaline Steeping Lye.

The reuse of steeping lye is crucial for the sustainable production of viscose fibers. Steeping lye contains hemicellulose and many alkaline degradation products, such as organic acids, so that its purification can be evaluated in terms of total organic carbon removal. When considering purification by membrane filtration, intermolecular interactions between hemicellulose and organic acids can strongly affect their retention efficiency.

Improving molar mass analysis of cellulose samples with limited solubility.

Fully dissolved cellulose samples are a requirement for reliable size exclusion chromatography (SEC). Although most of the standard dissolving pulps can be completely dissolved in the N,N-dimethylacetamide/lithium chloride (DMAc/LiCl) solvent system, some cellulose samples (e.g.

Enzymatic pulp upgrade for producing high-value cellulose out of a Kraft paper pulp.

The high-yield separation of polymeric parts from wood-derived lignocellulosic material is indispensable in biorefinery concepts. For the separation of cellulose and xylan from hardwood paper pulps to obtain pulps of high cellulose contents, simple alkaline extractions were found to be the most suitable technology, although having certain limitations. These are embodied by residual alkali resistant xylan incorporated in the pulp matrix.

How spectroscopy and microspectroscopy of degraded wood contribute to understand fungal wood decay.

Nuclear magnetic resonance, mid and near infrared, and ultra violet (UV) spectra of wood contain information on its chemistry and composition. When solid wood samples are analysed, information on the molecular structure of the lignocellulose complex of wood e.g.

Localisation and characterisation of incipient brown-rot decay within spruce wood cell walls using FT-IR imaging microscopy.

Spruce wood that had been degraded by brown-rot fungi (Gloeophyllum trabeum or Poria placenta) exhibiting mass losses up to 16% was investigated by transmission Fourier transform infrared (FT-IR) imaging microscopy. Here the first work on the application of FT-IR imaging microscopy and multivariate image analysis of fungal degraded wood is presented and the first report on the spatial distribution of polysaccharide degradation during incipient brown-rot of wood. Brown-rot starts to become significant in the outer cell wall regions (middle lamellae, primary cell walls, and the outer layer of the secondary cell wall S1).

Qualitative and quantitative changes of beech wood degraded by wood-rotting basidiomycetes monitored by Fourier transform infrared spectroscopic methods and multivariate data analysis.

Beech wood (Fagus sylvatica L.) veneers were cultivated with white and brown rot fungi for up to 10 weeks. Fungal wood modification was traced with Fourier transform near infrared (FT-NIR) and Fourier transform mid infrared (FT-MIR) methods.