Analysis of products from the oxidation of technical lignins by oxygen and H3PMo12O40 in water and aqueous methanol by size-exclusion chromatography

One kraft lignin and two lignosulfonates were oxidized in aqueous acidic solutions containing a polyoxometalate (POM). The degradations were carried out in H2O or MeOH/H2O mixtures in the presence of oxygen. The treatment with aqueous H3PMo12O40 led to the dissolution of the studied lignins in the acidic medium (pH 1-2) and to the formation of up to 6.5 wt% vanillin and 6.2 wt% methyl vanillate based on the weight of dry lignin. The lignin oxidation products were analyzed by size-exclusion chromatography (SEC). For this purpose, a SEC method was developed, which allows the analysis of kraft lignin, lignosulfonates, and reaction products thereof without the need to remove the homogeneous catalyst. This method allows the direct observation of depolymerization and repolymerization reactions and hence the provision of a tool for studying the underlying chemistry. It has been demonstrated that the depolymerization of kraft lignin in water is accompanied by counterproductive condensation reactions. These repolymerization reactions were effectively prevented by addition of methanol, which couples competitively with lignin intermediate

Acidic oxidation of kraft lignin into aromatic monomers catalyzed by transition metal salts

As one of the three main components in woody biomass, lignin is an abundant but underused renewable raw material and carbon source. Owing to its aromatic structure and large availability as a by-product of pulping, its conversion into chemicals is highly attractive. In the present work, the oxidation of a softwood kraft lignin in acidic media was investigated in the presence of a homogeneous catalyst. The objective was to find a cheap but efficient catalyst for the depolymerization of kraft lignin into aromatic monomers. Different transition metal salts were screened and compared to phosphomolybdic acid, which was investigated in previous studies, and to experiments in sulfuric acid without additional catalyst. Vanillin and methyl vanillate were the main monomeric products detected by gas chromatography/mass spectrometry but their formation was only slightly increased by using transition metal salts (up to 6.28 wt% yield). However, the presence of iron or copper chloride resulted in fast formation kinetics and significant amounts of other monomeric products. In addition, an efficient fragmentation of the lignin molecule from a weight-average molecular weight of 3500g mol-1 down to 500g mol-1 was observed by size-exclusion chromatography. The enhanced incorporation of oxygen into the reaction products in the presence of those catalysts was proven by Fourier transform infrared spectroscopy and the influence of the catalyst concentration was studie

Demonstration of a Process for the Conversion of Kraft Lignin into Vanillin and Methyl Vanillate by Acidic Oxidation in Aqueous Methanol

In this work, a process for producing vanillin and methyl vanillate from an industrial kraft lignin by oxidation in aqueous methanol at acidic pH is proposed. A series of consecutive runs, comprising the steps of kraft lignin oxidation, monomer extraction, and filtration of residual lignin, were conducted. The depolymerization of kraft lignin (1 g per run) was carried out in a stirred batch reactor with 80 vol % methanol/water as the solvent, with H3PMo12O40 as a homogeneous catalyst, and with 10 bar of oxygen initially present. The monomeric products were recovered from the process by extraction with chloroform and quantified by gas chromatography/mass spectrometry (GC/MS). Residual kraft lignin was recovered from the reaction medium by filtration. After extraction and filtration, the reaction medium, containing the homogeneous catalyst, was reused in the next run. The sum of all quantified products (gas phase, extract, and solids), as well as the amount of consumed oxygen, reached constant levels after five runs, and no indications of catalyst deactivation were found. Extracted products containing vanillin (3.5 wt %) and methyl vanillate (3.5 wt %) were recovered with a yield of 65 wt %. The extracted products were further analyzed by size exclusion chromatography (SEC) and Fourier transform infrared (FTIR) spectroscopy regarding their average molecular weight and functional group contents

Analysis of products from the oxidation of technical lignins by oxygen and H3PMo12O40 in water and aqueous methanol by size-exclusion chromatography

Abstract One kraft lignin and two lignosulfonates were oxidized in aqueous acidic solutions containing a polyoxometalate (POM). The degradations were carried out in H2O or MeOH/H2O mixtures in the presence of oxygen. The treatment with aqueous H3PMo12O40 led to the dissolution of the studied lignins in the acidic medium (pH 1–2) and to the formation of up to 6.5 wt% vanillin and 6.2 wt% methyl vanillate based on the weight of dry lignin. The lignin oxidation products were analyzed by size-exclusion chromatography (SEC). For this purpose, a SEC method was developed, which allows the analysis of kraft lignin, lignosulfonates, and reaction products thereof without the need to remove the homogeneous catalyst. This method allows the direct observation of depolymerization and repolymerization reactions and hence the provision of a tool for studying the underlying chemistry. It has been demonstrated that the depolymerization of kraft lignin in water is accompanied by counterproductive condensation reactions. These repolymerization reactions were effectively prevented by addition of methanol, which couples competitively with lignin intermediates.</jats:p

Acidic oxidation of kraft lignin into aromatic monomers catalyzed by transition metal salts

ISSN:0018-3830ISSN:1437-434