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The objective of this work was to determine the effect of sodium methyl mercaptide (SMM) as an additive on the minimization of carbohydrate peeling reactions in Rock/Hard Maple (Acer saccharum) chips during kraft pulping. Two methods were evaluated for SMM addition to the pulping process: 1) pre-treatment before pulping and 2) co-addition with white liquor. The experimental results showed about 2.5% (on wood basis) increase in the kraft pulp yield after pre-treatment with 4.38% SMM (on wood basis) or the co-addition of the same amount of SMM with white liquor. The use of 4.38% SMM allowed a decrease in the white liquor effective alkali charge of 3% (on wood basis) to produce the target 14–15 kappa pulp. The 4.38% SMM charge was determined to be the optimum for both pre-treatment and co-addition. The increase in kraft pulp yield was mostly due to increased retention of cellulose (about 0.8% on wood) and xylan (about 1.8% on wood). The retention of glucomannan was insignificant in all cases. Based on the increase in intrinsic viscosity, it is concluded that the increased cellulose yield with SMM addition is caused by both reduced primary peeling and faster delignification rate (less alkaline hydrolysis followed by secondary peeling). The increased xylan retention is due to the lower effective alkali concentration during kraft pulping with SMM addition. [ABSTRACT FROM AUTHOR]

A mixture of US southern hardwood chips was treated with aqueous acetic and formic acid (FA) solutions in a modified Dionex ASE100 extractor. The amount and selectivity of hemicelluloses dissolution increase at higher acetic acid (AA) and FA concentrations, but cellulose remains intact in the residual wood. Even at the highest AA concentration of 100 g l-¹, the dissolved hemicellulose fragments are still oligomeric except for arabinose. The formation of lignin-like condensation products (LCPs) and decomposition of dissolved mannose, arabinose, and galactose were observed at the highest AA concentration. Sugar hydrolysis is more pronounced with the addition of FA at increasing temperature. The concentration of xylose in the FA extract is approximately the same as that of xylooligomers at 160°C. Formation of LCPs is only observed at 170°C during 10 g l-¹ FA treatment. The concentrations of dissolved wood components increase linearly with increased recycling of the FA extract. [ABSTRACT FROM AUTHOR]

The overall target of this project, called Bioforest, is to develop an economic process for the production of commodity chemicals from mixed forest biomass, consisting of logging residues of hardwoods (HW) and softwoods (SW) and also from recycled fibers. The aim is to dissolve the biomass lignin and to produce monosugars based on hemicelluloses and hydrolyzed cellulose in high yield. The hydrolyzate could subsequently be converted into chemicals by modified acetone-butanol-ethanol fermentation. Here, the total mass balances of SO2-ethanol-water fractionation of different types of biomass feedstocks, such as SW and HW biomass, and deinked pulp are presented. Chemical composition of the feedstocks, solid residues (pulps) and spent liquors of fractionation were analyzed to gain more understanding about the fractionation procedure. The analysis was focused on carbohydrates, lignin, ash, acetyl groups and sugar degradation products. It was also examined if all feedstocks could be treated simultaneously in one digester because a larger feedstock supply within an economic transport radius improves the viability of the process. The fractionation approach was successful and it can be concluded that the method presented is very versatile for future applications in lignocellulosic biorefineries. [ABSTRACT FROM AUTHOR]