Fate of Residual Lignin during Delignification of Kraft Pulp by Trametes versicolor

1998 ◽  
Vol 64 (6) ◽  
pp. 2117-2125 ◽  
Author(s):  
Ian D. Reid
Keyword(s):  
Trametes Versicolor ◽  
Kraft Pulp ◽  
Lignin Degradation ◽  
Water Soluble ◽  
Kraft Pulps ◽  
Residual Lignin ◽  
Spruce Wood ◽  
Single Ring ◽  
Enzyme Bleaching ◽  
By Products

ABSTRACT The fungus Trametes versicolor can delignify and brighten kraft pulps. To better understand the mechanism of this biological bleaching and the by-products formed, I traced the transformation of pulp lignin during treatment with the fungus. Hardwood and softwood kraft pulps containing 14C-labelled residual lignin were prepared by laboratory pulping of lignin-labelled aspen and spruce wood and then incubated with T. versicolor. After initially polymerizing the lignin, the fungus depolymerized it to alkali-extractable forms and then to soluble forms. Most of the labelled carbon accumulated in the water-soluble pool. The extractable and soluble products were oligomeric; single-ring aromatic products were not detected. The mineralization of the lignin carbon to CO2 varied between experiments, up to 22% in the most vigorous cultures. The activities of the known enzymes laccase and manganese peroxidase did not account for all of the lignin degradation that took place in the T. versicolor cultures. This fungus may produce additional enzymes that could be useful in enzyme bleaching systems.

Changes in the lignin-carbohydrate complex in softwood kraft pulp during kraft and oxygen delignification

Holzforschung ◽  
2004 ◽  
Vol 58 (6) ◽  
pp. 603-610 ◽  
Author(s):  
Martin Lawoko ◽  
Rickard Berggren ◽  
Fredrik Berthold ◽  
Gunnar Henriksson ◽  
Göran Gellerstedt
Keyword(s):  
Kraft Pulp ◽  
Kappa Number ◽  
Kraft Pulps ◽  
Residual Lignin ◽  
Oxygen Delignification ◽  
Number Range ◽  
Morphological Aspects ◽  
Carbohydrate Complex ◽  
Softwood Kraft Pulp ◽  
Hydrolysis Of

Abstract Three kraft pulps in the kappa number range between 50 and 20 and the same pulps oxygen-delignified to similar lignin contents (kappa approximately 6) were analyzed for lignin-carbohydrate complexes (LCC) by a method based on selective enzymatic hydrolysis of the cellulose, and quantitative fractionation of the LCC. Between 85 and 90% of residual lignin in the unbleached kraft pulp and all residual lignin in the oxygen-delignified pulps were isolated as LCC. Three types of complexes were found; viz., xylan-lignin, glucomannan-lignin-xylan and glucanlignin complexes. After pulping to a high kappa number, most of the residual lignin was linked to xylan. Different delignification rates were observed so that most of the residual lignin was linked to glucomannan when the pulping was extended to a low kappa number. With increasing degree of oxygen delignification, a similar trend in the delignification rates of LCC was observed so that the residual lignin was increasingly linked to glucomannan. Complex LCC network structures seemed to be degraded into simpler structures during delignification. The differences in delignification rates are discussed with reference to the solubility properties and structural differences of LCC, and to morphological aspects of the pulp.

Oxygen Delignification of High-Yield Kraft Pulp. Part I: Structural Properties of Residual Lignins

Holzforschung ◽  
1999 ◽  
Vol 53 (4) ◽  
pp. 416-422 ◽  
Author(s):  
Størker T. Moe ◽  
Arthur J. Ragauskas
Keyword(s):  
Carboxylic Acid ◽  
Acid Hydrolysis ◽  
Extraction Method ◽  
Kraft Pulp ◽  
Kraft Pulping ◽  
High Yield ◽  
Kraft Pulps ◽  
Residual Lignin ◽  
Oxygen Delignification ◽  
Carboxylic Acid Groups

Summary The chemistry of oxygen delignification of high-yield kraft pulp was studied by analysis of residual lignin extracted from kraft and kraft-oxygen pulps using the acid hydrolysis/dioxane extraction method. For reference pulps cooked to kappa numbers between 20 and 25, the content of free phenolic groups decreased to about 50% the original value upon oxygen delignification, while the content of carboxylic acid groups increased by 50–100%. For lignins isolated from high-yield kraft pulp and oxygen delignified high-yield kraft pulp, it was shown that high-yield kraft pulping with polysulfide (PS) and anthraquinone (AQ) gives a residual lignin which is chemically different from that of kraft pulps cooked to lower kappa numbers. Lignin extracted from oxygen delignified high-yield PS/AQ kraft pulp was more similar to lignins extracted from kraft pulps cooked to lower kappa numbers.

An improved procedure for isolation of residual lignins from hardwood kraft pulps

Holzforschung ◽  
2004 ◽  
Vol 58 (5) ◽  
pp. 464-472 ◽  
Author(s):  
Ewellyn Augsten Capanema ◽  
Mikhail Yurievich Balakshin ◽  
Chen-Loung Chen
Keyword(s):  
Molecular Mass ◽  
Nitrogen Content ◽  
Mass Distribution ◽  
Kraft Pulp ◽  
Molecular Mass Distribution ◽  
Eucalyptus Grandis ◽  
Kraft Pulps ◽  
Carbohydrate Composition ◽  
Residual Lignin ◽  
Hydrolysis Of

Abstract Residual lignin preparations were isolated from birch, aspen and Eucalyptus grandis kraft pulp by enzymatic hydrolysis of the pulps with cellulase:hemicellulase mixture. Residual lignin preparations were characterized by investigation of nitrogen content, carbohydrate composition and molecular mass distribution. The use of enzyme with high activity and optimization of enzyme charge resulted in significant decrease in protein contaminants in residual lignin preparations as compared to previously published results. A second order law correlation between enzyme mass charge and nitrogen content in birch residual lignin preparations indicates a strong effect of enzyme charge on the amount of protein contaminants. However, the enzyme charge in the range studied does not appreciably affect either the yields of the residual lignin preparations or percentage and composition of carbohydrates in these preparations. The optimal enzyme charge was highest for Eucalyptus grandis pulp and lowest for birch pulp. It has been suggested that a significant part of the hardwood residual lignin in pulps, especially in E. grandis pulp, consists of low molecular mass lignin fragments bonded to pulp carbohydrates. Higher amount of glucose in E. grandis residual lignin preparation compared to those from birch and aspen implied a higher frequency of lignin-cellulose bonds in eucalypt pulp. Different fractions of birch residual lignin have rather similar molecular mass distribution, which was not affected by the charge of the enzyme. Eucalypt residual lignin preparation had higher molecular mass than birch residual lignin.

Size exclusion chromatographic and UV-VIS absorption analyses of unbleached and bleached softwood kraft pulps using LiCl/1,3-dimethyl-2-imidazolidinone as a solvent

Holzforschung ◽  
2007 ◽  
Vol 61 (3) ◽  
pp. 236-241 ◽  
Author(s):  
Masahiro Yanagisawa ◽  
Akira Isogai
Keyword(s):  
Kraft Pulp ◽  
Total Yield ◽  
Degree Of Polymerization ◽  
Size Exclusion ◽  
Kraft Pulps ◽  
Residual Lignin ◽  
Light Scattering Detection ◽  
Exclusion Chromatography ◽  
Photodiode Array ◽  
Sulfite Pulp

Abstract Unbleached and bleached kraft pulps and holocellulose prepared from softwood were totally soluble in 8% LiCl/1,3-dimethyl-2-imidazolidinone (LiCl/DMI). The solutions were analyzed by size exclusion chromatography with photodiode array and multi-angle laser light scattering detection (SEC-PDA-MALLS). The mobile phase consisted of 1% LiCl/DMI. The degree of polymerization (DP) and DP distribution of the softwood kraft pulps were determined, as well as the DP distribution of residual lignins based on their UV-VIS absorption patterns. Changes in DP for kraft pulps after a conventional bleaching sequence were evaluated, and the residual lignins were analyzed in the same way. Approximately half of the residual lignin in unbleached and bleached kraft pulps was present in polysaccharide fractions with high DP, which represented approximately 90% of the total yield. Some characteristic differences in the UV-VIS absorption pattern were observed between kraft pulps bleached with oxygen and chlorine. DP, DP distribution of polysaccharides, and distribution of residual lignin were clearly different for unbleached kraft pulp, unbleached sulfite pulp, and holocellulose. An unbleached kraft pulp prepared from hardwood showed different properties to the corresponding softwood preparation. The UV-VIS absorption patterns due to residual lignins were also very characteristic for the various pulps and holocellulose.

Elucidating carboxylic acid profiles for extended oxygen delignification of high-kappa softwood kraft pulps

Holzforschung ◽  
2006 ◽  
Vol 60 (2) ◽  
pp. 123-129 ◽  
Author(s):  
Dongcheng Zhang ◽  
Yunqiao Pu ◽  
Xing-Sheng Chai ◽  
Ved Naithani ◽  
Hasan Jameel ◽  
...  
Keyword(s):  
Carboxylic Acid ◽  
Acid Content ◽  
Kraft Pulp ◽  
Lignin Content ◽  
Acid Group ◽  
Kraft Pulps ◽  
Residual Lignin ◽  
Oxygen Delignification ◽  
Acid Ratio ◽  
Softwood Kraft Pulp

Abstract Two laboratory high-lignin-content softwood (SW) kraft pulps with kappa values of 48.0 and 49.5, prepared by cooking at high and low active alkali (AA), were used for the study of fiber charge development during two-stage oxygen delignification with inter-stage washing (OwO). It was established that the first oxygen delignification (O) stage increased total fiber charge by 2–4%, and further O-delignification via a second O-stage led to a 3–18% decrease in total fiber charge. Carboxylic acid content in pulp holocelluloses decreased by 12–26% with respect to a 35–70% kappa number reduction due to an O and OwO stage of delignification for high and low AA cooked SW kraft pulps. After an OwO-stage delignification, the residual lignin was found to exhibit a 50–100% increase in carboxylic acid content. 13C NMR spectral data for the residual lignin samples indicated that the unconjugated/conjugated acid ratio was approximately (3–4):1. Generally, the carboxylic acid content in low AA cooked softwood kraft pulp and the corresponding oxygen-delignified pulps was systematically higher (13–23%) than that in high AA cooked SW kraft pulp and the corresponding oxygen-delignified pulps. The experimental results also demonstrated that maximum acid-group content in total fiber occurred after 45–50% oxygen delignification of the SW kraft pulps studied.

Prebleaching of eucalypt kraft pulp with OP stages: Effect of an acid pretreatment or chelation step

TAPPI Journal ◽  
2012 ◽  
Vol 11 (6) ◽  
pp. 31-38
Author(s):  
TATIANA M. PÓVOAS ◽  
DINA A.G. ANGÉLICO ◽  
ANA P.V. EGAS ◽  
PEDRO E.G. LOUREIRO ◽  
LICÍNIO M. GANDO-FERREIRA ◽  
...  
Keyword(s):  
Eucalyptus Globulus ◽  
Comparative Evaluation ◽  
Kraft Pulp ◽  
Kraft Pulps ◽  
Acid Pretreatment ◽  
High Brightness ◽  
Pulp Viscosity ◽  
Brightness Reversion

We conducted a comparative evaluation of different treatments for the bleaching of eucalypt kraft pulps beginning with OP stages. The treatments tested were (1) an acid chelation stage with DTPA (OQP sequence); (2) a hot acid stage (AOP sequence); and (3) a chelant addition into the alkaline oxygen stage ((OQ)P and A(OQ)P sequences). The latter strategy was also studied for environmental reasons, as it contributes to the closure of the filtrate cycle. The OQP sequence leads to the highest brightness gain and pulp viscosity and the lowest peroxide consumption caused by an efficient metals control. Considering that the low biodegradability of the chelant is a problem, the A(OQ)P sequence is an interesting option because it leads to reduced peroxide consumption (excluding OQP) while still reaching high brightness values and similar brightness reversion to OQP prebleaching, with only a viscosity loss of 160 dm3/kg. Therefore, a hot acid stage could be considered when a separate acid Q stage is absent in a prebleaching sequence of Eucalyptus globulus kraft pulps involving OP stages.

Optimization of elemental chlorine-free bleaching for a softwood kraft pulp • part 2: economic analysis of chemical and steam consumption

TAPPI Journal ◽  
2010 ◽  
Vol 9 (9) ◽  
pp. 47-53 ◽  
Author(s):  
BRIAN N. BROGDON
Keyword(s):  
Chlorine Dioxide ◽  
Previous Investigation ◽  
Kraft Pulp ◽  
Energy Costs ◽  
Alkaline Extraction ◽  
Stage Versus ◽  
Kraft Pulps ◽  
Steam Consumption ◽  
Elemental Chlorine ◽  
Softwood Kraft Pulp

Our previous investigation [1] re-analyzed the data from Basta and co-workers (1992 TAPPI Pulping Conference) to demonstrate how oxidative alkaline extraction can be augmented and how these changes affect chlorine dioxide consumption with elemental chlorine-free (ECF) sequences. The current study manipulates extraction delignification variables to curtail bleaching costs with a conventional U.S. Southern softwood kraft pulp. The economic advantages of ~0.35% to 0.65% H2O2 peroxide reinforcement in a 70°C (EOP)-stage versus 90°C (EO)-stage are predisposed to the brightness targets, to short or long bleach sequences, and to mill energy costs. Minimized bleaching costs are generally realized when a 90°C (EO) is employed in D0(EO)D1 bleaching, whereas a 70°C (EOP) is economically advantageous for D0(EOP)D1E2D2 bleaching. The findings we disclose here help to clarify previous ECF optimization studies of conventional softwood kraft pulps.

scholarly journals Analytical Characterization of Water-Soluble Constituents in Olive-Derived By-Products

Foods ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 1299
Author(s):  
Pablo Doménech ◽  
Aleta Duque ◽  
Isabel Higueras ◽  
José Luis Fernández ◽  
Paloma Manzanares
Keyword(s):  
Olive Tree ◽  
Mediterranean Area ◽  
Water Soluble ◽  
Olive Pomace ◽  
Olive Leaves ◽  
Olive Stone ◽  
Olive Trees ◽  
Tree Pruning ◽  
By Products

Olive trees constitute one of the largest agroindustries in the Mediterranean area, and their cultivation generates a diverse pool of biomass by-products such as olive tree pruning (OTP), olive leaves (OL), olive stone (OS), and extracted olive pomace (EOP). These lignocellulosic materials have varying compositions and potential utilization strategies within a biorefinery context. The aim of this work was to carry out an integral analysis of the aqueous extractives fraction of these biomasses. Several analytical methods were applied in order to fully characterize this fraction to varying extents: a mass closure of >80% was reached for EOP, >76% for OTP, >65% for OS, and >52% for OL. Among the compounds detected, xylooligosaccharides, mannitol, 3,4-dihydroxyphenylglycol, and hydroxytyrosol were noted as potential enhancers of the valorization of said by-products. The extraction of these compounds is expected to be more favorable for OTP, OL, and EOP, given their high extractives content, and is compatible with other utilization strategies such as the bioconversion of the lignocellulosic fraction into biofuels and bioproducts.

scholarly journals Biodegradation of Chloroxylenol by Cunninghamella elegans IM 1785/21GP and Trametes versicolor IM 373: Insight into Ecotoxicity and Metabolic Pathways

2021 ◽  
Vol 22 (9) ◽  
pp. 4360
Author(s):  
Marta Nowak ◽  
Katarzyna Zawadzka ◽  
Janusz Szemraj ◽  
Aleksandra Góralczyk-Bińkowska ◽  
Katarzyna Lisowska
Keyword(s):  
Trametes Versicolor ◽  
Significant Rise ◽  
Pcr Analysis ◽  
Cunninghamella Elegans ◽  
Oxidation Reactions ◽  
Cytochrome P450 Enzymes ◽  
C Elegans ◽  
Real Time Quantitative Pcr ◽  
Genes Expression ◽  
By Products

Chloroxylenol (PCMX) is applied as a preservative and disinfectant in personal care products, currently recommended for use to inactivate the SARS-CoV-2 virus. Its intensive application leads to the release of PCMX into the environment, which can have a harmful impact on aquatic and soil biotas. The aim of this study was to assess the mechanism of chloroxylenol biodegradation by the fungal strains Cunninghamella elegans IM 1785/21GP and Trametes versicolor IM 373, and investigate the ecotoxicity of emerging by-products. The residues of PCMX and formed metabolites were analysed using GC-MS. The elimination of PCMX in the cultures of tested microorganisms was above 70%. Five fungal by-products were detected for the first time. Identified intermediates were performed by dechlorination, hydroxylation, and oxidation reactions catalysed by cytochrome P450 enzymes and laccase. A real-time quantitative PCR analysis confirmed an increase in CYP450 genes expression in C. elegans cells. In the case of T. versicolor, spectrophotometric measurement of the oxidation of 2,20-azino-bis (3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) showed a significant rise in laccase activity during PCMX elimination. Furthermore, with the use of bioindicators from different ecosystems (Daphtoxkit F and Phytotoxkit), it was revealed that the biodegradation process of PCMX had a detoxifying nature.

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