Beech Wood Lignin Research Articles

Statistical evaluation of DPPH, ABTS, FRAP, and Folin-Ciocalteu assays to assess the antioxidant capacity of lignins

This research studies in detail four different assays, namely DPPH (2,2-diphenyl-1-picrylhydrazyl), ABTS (2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid)), FRAP (ferric ion reducing antioxidant potential) and FC (Folin-Ciocalteu), to determine the antioxidant capacity of standard substances as well as 50 organosolv lignins, and two kraft lignins. The coefficient of variation was determined for each method and was lowest for ABTS and highest for DPPH. The best correlation was found for FRAP and FC, which both rely on a single electron transfer mechanism. A good correlation between ABTS, FRAP and FC, respectively, could be observed, even though ABTS relies on a more complex reaction mechanism. The DPPH assay merely correlates with the others, implying that it reflects different antioxidative attributes due to a different reaction mechanism. Lignins obtained from paulownia and silphium have been investigated for the first time regarding their antioxidant capacity. Paulownia lignin is in the same range as beech wood lignin, while silphium lignin resembles wheat straw lignin. Miscanthus lignin is an exception from the grass lignins and possesses a significantly higher antioxidant capacity. All lignins possess a good antioxidant capacity and thus are promising candidates for various applications, e. g. as additives in food packaging or for biomedical purposes.

Enhanced depolymerization of beech wood lignin and its removal with peroxidases through continuous separation of lignin fragments

A study highlighting the benefits associated with the continuous separation of MnP- (or LiP-) depolymerized lignin fragments from the reaction medium using a membrane bioreactor.

In Vitro Fermentation of Beechwood Lignin-Carbohydrate Complexes Provides Evidence for Utilization by Gut Bacteria.

Lignin-carbohydrate complexes (LCCs) are emerging as a new and natural product with pharmacological and nutraceutical potential. It is uncertain, however, whether LCCs have a positive effect on the microbiota of the gut based on the current evidence. Here, the LCC extracted from beechwood (BW-LCC) was used as a substrate for in vitro fermentation. The lignin in BW-LCC consisted of guaiacyl (G) and syringyl (S) units, which are mainly linked by β-O-4 bonds. After 24 h of in vitro fermentation, the pH had evidently declined. The concentrations of acetic acid and propionic acid, the two main short-chain fatty acids (SCFAs), were significantly higher than in the control group (CK). In addition, BW-LCC altered the microbial diversity and composition of gut microbes, including a reduction in the relative abundance of Firmicutes and an increase in the relative abundance of Proteobacteria and Bacteroidetes. The relative abundance of Escherichia coli-Shigella and Bacteroides were the most variable at the genus level. The genes of carbohydrate-active enzymes (CAZymes) also changed significantly with the fermentation and were related to the changes in microbes. Notably, the auxiliary actives (AAs), especially AA1, AA2, and AA3_2, play important roles in lignin degradation and were significantly enriched and concentrated in Proteobacteria. From this study, we are able to provide new perspectives on how gut microbes utilize LCC.

In situ formation of fatty acid methyl esters via thermally assisted methylation by lignin during torrefaction of oil palm biomass

Torrefaction of oil palm empty fruit bunch (EFB) biomass was performed at six temperatures between 210 and 360 °C. The composition of the evolved and trapped condensates was analyzed by GC/MS and the torrefied biomass samples were characterized by pyrolysis-GC/MS (Py-GC/MS). The analyses showed that the thermal treatment of the biomass produced significant amounts of fatty acid methyl esters (FAMEs). The in situ FAME formation was explained by the reaction of the lipid and lignin contents of the biomass; i.e., the fatty acid moieties of triglycerides were methylated by the methoxy side groups of lignin during the thermal treatment. The reaction was verified by the pyrolysis of a model mixture, using Py-GC/MS and thermogravimetry/mass spectrometry, which consisted of the EFB lipid extract and an isolated beech wood lignin. Demethylation of lignin resulted changes in its thermal decomposition; smaller amounts of 4-methylguaiacol and 4-methylsyringol were evolved and the char yield was increased. The GC/MS analysis of the EFB condensates showed that FAME conversion was the highest and the sources of fatty acid moieties were depleted if the torrefaction temperature had been set at and above 330 °C. The free fatty acid content of EFB was relatively high, which evaporated at lower temperatures before the rate of FAME formation increased between 270 and 300 °C. In comparison with torrefaction, only a small portion of FAMEs formed during the flash pyrolysis of raw EFB at 450 °C indicating that the prolonged heating of the oily biomass favors the FAME formation. Pyrolysis-GC/MS measurements of the torrefied samples showed that the triglyceride residue could also be utilized if the torrefaction as pretreatment was performed at or below 300 °C. In addition, torrefaction increased the accessibility of the biomass components for FAME formation. Some other fatty acid derivatives (i.e., ketone, hydrocarbon, amide, and nitrile) were also detected in smaller amounts. The phenomenon of in situ FAME formation during pyrolysis might be a useful process to enhance pyrolytic biomass utilization by producing FAMEs as additional fuel products and increasing the char yield simultaneously.

Catalytic fast pyrolysis of beech wood lignin isolated by different biomass (pre)treatment processes: Organosolv, hydrothermal and enzymatic hydrolysis

Lignin is one of the three main structural components of lignocellulosic biomass and is considered as the most abundant source of aromatic and phenolic compounds. Lignin is produced as side-stream in the pulp/paper industry or as residue in the production of second-generation bioethanol. More recently, novel biomass fractionation processes in biorefineries have been developed aiming at the production of high quality/purity lignin towards its more efficient down-stream catalytic conversion to chemicals, monomers, and fuels. Within this context, in this work, we studied the thermal (non-catalytic) and catalytic fast pyrolysis on a Py/GC–MS system and a fixed-bed reactor unit of three types of lignin, all originating from the same biomass (beech wood sawdust) but with different isolation processes: organosolv lignin derived by the organosolv pretreatment/fractionation of biomass, surface extracted lignin derived by the mild Soxhlet extraction (with ethanol or acetone) from the hydrothermally (HT) in pure water pretreated biomass, and the enzymatic hydrolysis lignin derived as a lignin-rich solid residue from the enzymatic hydrolysis of the HT pretreated biomass. Conventional microporous ZSM-5 and mesoporous ZSM-5 zeolites (with intracrystal mesopores, ˜ 9 nm) were used as catalysts in the pyrolysis experiments. Both zeolites were very active in converting the initially produced via thermal pyrolysis methoxy-substituted phenols, benzenes and benzaldehydes mainly towards BTX mono-aromatics, such as 1,3-dimethylbenzene/p- and o-xylenes, toluene and trimethylbenzenes, as well as polycyclic aromatic hydrocarbons (PAHs, mainly naphthalenes). The mesoporous ZSM-5 induced higher dealkoxylation reactivity compared to the microporous ZSM-5 leading to higher concentration of BTX aromatics without a consequent increase of PAHs. The pronounced dealkoxylation/aromatization reactivity of both ZSM-5 zeolites resulted to lower yields (but highly aromatic) organic bio-oils (e.g. from 32−35 wt.% to 15−22 wt.%) compared to thermal pyrolysis, increased non-condensable gases (mainly CO, CO2, methane, ethylene and propylene) and formation of relatively low amounts of coke on catalysts (e.g. 3−5 wt.% on lignin) in addition to thermal pyrolysis char. The observed moderate variations in the characteristics of the three types of beech wood lignin, i.e. molecular weight (GPC), S/G ratio, inter-unit linkages (2D HSQC NMR) and elemental composition, did not induce a systematic/substantial differentiation in the thermal and catalytic fast pyrolysis product yields and composition.

Laccase-induced HBT-grafting to milled beech wood reduces unspecific protein adsorption

Lignocellulosic biomass is a ubiquitous and renewable feedstock for the production of platform chemicals and biofuels. Typically, this recalcitrant biomass is pretreated by physico-chemical techniques causing disintegration and delignification. An additional treatment with laccase-mediator-systems (LMS) has been found to further improve the subsequent enzymatic cellulose hydrolysis. The aim of this study was to investigate the impact of different LMS on the glucose yield of a subsequent hydrolysis of treated beech wood and to elucidate the underlying effect of LMS treatment. The mediators 2,2′-azino-bis-3-ethylbenzothiazoline-6-sulphonic acid (ABTS), 1-hydroxybenzotriazol (HBT) and syringaldehyde were evaluated, but an enhancing effect of LMS treatment on beech wood hydrolysis was only found for HBT. In mass spectrometry analysis of the acid hydrolysate of LMS-treated samples, the mediator HBT could be found in the lignin samples, suggesting a grafting reaction. The fluorescent protein mCherry was used as a reporter for unspecific protein adsorption to biomass samples. LMS treatment with HBT reduced the unspecific adsorption of mCherry to raw beech wood by about 50%, suggesting that the HBT grafting to beech wood lignin decreased the unproductive cellulase binding. In summary, the reduction of unspecific protein adsorption by biomass surface modification with laccase-HBT treatment is proposed to be the underlying mechanism for increased cellulose conversion.

Organocatalytic Chemoselective Primary Alcohol Oxidation and Subsequent Cleavage of Lignin Model Compounds and Lignin.

A one-pot two-step degradation of lignin β-O-4 model compounds initiated by preferred oxidation of the primary over the secondary hydroxyl groups with a TEMPO/DAIB system has been developed [TEMPO=2,2,6,6-tetramethylpiperidine-N-oxyl, DAIB=(diacetoxy)iodobenzene]. The oxidised products are then cleaved by proline-catalysed retro-aldol reactions. This degradation methodology produces simple aromatics in good yields from lignin model compounds at room temperature with an extension to organosolv beech-wood lignin (L1) resulting in known cleavage products.

Effects of overexpression of PKAc genes on expressions of lignin-modifying enzymes by Pleurotus ostreatus.

We studied the role of genes encoding the cAMP-dependent protein kinase A catalytic subunit (PKAc) in the ligninolytic system in Pleurotus ostreatus. The wild-type P. ostreatus strain PC9 has two PKAc-encoding genes: PKAc1 and PKAc2 (protein ID 114122 and 85056). In the current study, PKAc1 and PKAc2 were fused with a β-tubulin promoter and introduced into strain PC9 to produce the overexpression strains PKAc1-97 and PKAc2-69. These strains showed significantly higher transcription levels of isozyme genes encoding lignin-modifying enzymes than strain PC9, but the specific gene expression patterns differed between the two recombinant strains. Both recombinants showed 2.05-2.10-fold faster degradation of beechwood lignin than strain PC9. These results indicate that PKAc plays an important role in inducing the wood degradation system in P. ostreatus.

Qualitative and Quantitative Analysis of Lignin Produced from Beech Wood by Different Conditions of the Organosolv Process

Lignins in general have been extensively studied, while beech wood lignin in particular is rarely researched. In the present work, Organosolv isolated lignin from beech wood (OBL) has been characterized. The isolation was done by two methods: (a) by using sulfuric acid at 170 °C and a reaction time of 120 min and (b) at a temperature of 180 °C for 240 min. A range of analytical methods were applied including elemental analysis, FT-IR, UV–Vis, 31P NMR, SEC, Pyrolysis-GC/MS and HPLC to gain information about establish the purity, structure, molecular weight, thermal behavior and to determine carbohydrate residues according to the NREL protocol. FT-IR and UV–Vis spectra of OBL revealed expected typical absorptions for lignins. NREL analysis presented a carbohydrate-free lignin fraction which has not been achieved to date. TGA and DSC are used to study the thermal behavior of the isolated lignins and showed a relatively low glass transition temperatures (Tg: 123 °C) and decomposition temperatures of 348 and 381 °C. The pyrograms generated from the pyrolysis–GC/MS at 550 °C consisted mainly of fragments of syringyl, guaiacyl and hydroxyphenyl units, thereby confirming the results of the NMR analysis. Our findings support Organolsolv as an efficient method to isolate pure lignin fractions from beech wood with practical value in industry.

The Characteristics and Reactivity of Acid-Labile Aryl Ether Units in Wood Lignin

Wood lignin contains significant amounts of acid-labile aryl ether units, which play a significant role in lignin modification or delignification processes. We have evaluated the rate and reaction kinetics on the acid-catalyzed cleavages of aryl ether structures for wood lignin in situ based on the formation of phenolic hydroxyl groups. The content of acid-labile aryl ether units was quite uniform for a variety of softwood wood lignins (∼4% per C9 unit) and it varied appreciably among hardwood species, ranging from 4% for aspen to 9% for beech wood lignin. These variations, however, appear to be related to the content of syringyl units in wood lignin. The reactivity of these reactive aryl ether structures was noticeably higher for the spruce than for the aspen wood lignin. This difference in reactivity, based on the behavior of lignin model compound reactions, can be attributed to the influence of syringyl moieties in aspen wood lignin. It appears that most of the acid-labile aryl ether units in hardwood were associated with the syringy moiety being present as a benzyl unit, which is much less reactive than the corresponding guaiacyl moiety.

Retraction: Pan, T., Yu, Q., and Lloyd, S. (2013). “Quantum-chemistry–based study of beech-wood lignin as an antioxidant of petroleum asphalt.” J. Mater. Civ. Eng. , 25(10), 1477–1488; DOI:10.1061/(ASCE)MT.1943-5533.0000684

Retraction: Pan, T., Yu, Q., and Lloyd, S. (2013). “Quantum-chemistry–based study of beech-wood lignin as an antioxidant of petroleum asphalt.” <i>J. Mater. Civ. Eng.</i> , 25(10), 1477–1488; DOI:10.1061/(ASCE)MT.1943-5533.0000684

Retracted: Quantum-Chemistry–Based Study of Beech-Wood Lignin as an Antioxidant of Petroleum Asphalt

Oxidative hardening or aging of asphalt binder can lead to increase in viscosity, separation of components, loss of cohesion and adhesion, and eventually the degraded engineering performances. A common practice to minimize asphalt aging has been to use chemical additives or modifiers as antioxidants. The current state of knowledge in asphalt oxidation and antioxidant evaluation concentrates on monitoring the degradation in asphalt’s physical properties, mainly the viscosity and ductility. Such practices although satisfying direct engineering needs does not contribute to the fundamental understanding of the asphalt aging and antiaging mechanisms. As such, this study was initiated to study the antioxidation mechanisms of bio-based additives, using the beech-wood lignin as an example, by developing a quantum-chemistry based chemophysical environment in which the various chemical reactions among asphalt components, antioxidative ingredients and oxygen molecules, as well as the incurred physical changes can be studied. The techniques of X-ray photoelectron spectroscopy (XPS) were used to prove the validity of the modified and unmodified asphalt models.

La-modified SBA-15/H2O2 systems for the microwave assisted oxidation of organosolv beech wood lignin

In this manuscript, the inuence of organosolv beech wood lignin (LOB) on its oxidative conver- sion to high added-value phenolic aldehydes is discussed. Environmental friendly and low-cost H 2 O 2 was used as the oxygen atom donor. � e catalyst was prepared by immobilizing Lanthanum com- pounds onto the periodic mesoporous channels of siliceous SBA-15. � e activity of the La/SBA-15 was investigated towards oxidation of LOB in the presence of hydrogen peroxide as oxidant with microwave irradiation. Considering the characteristics of LOB, an unexpected low syringaldehyde concentration at 10min of reaction time (1.47 g/L, corresponding to 15.66% yield) was obtained; the other major product was vanillin at 25min (0.78 g/L, i.e., 9.94% yield). � e high reactivity of syringyl nuclei may be pointed out as the main reason for the faster production and degradation of syringaldehyde in oxida- tion. Other low molecular weight phenolic products were found: vanillic acid, syringic acid and minor quantities of aceto-derivatives. � e prole of products concentration with the reaction time of catalytic oxidation with microwave irradiation are shown and discussed with reference to the investigated lignin features. � e mechanism of the microwave catalytic oxidation for LOB under alkaline conditions was proposed.

Investigation of the chemical modifications of beech wood lignin during heat treatment

Holocellulose, Klason lignin and milled wood lignin (MWL) of beech wood were extracted before and after heat treatment and analysed using CP MAS 13C NMR, 13C NMR, 31P NMR and size exclusion chromatography (SEC). Experimental results showed that the thermal treatment degrades hemicelluloses and affects lignin polymer through depolymerisation due mainly to cleavage of β-aryl-ether linkages and recondensation reactions. The spectroscopic analysis of MWL demonstrated that these recondensation reactions involved mainly guaiacyl units through formation of 5,5′-biphenolic and diarylmethane structures. Analysis of molecular weight distribution of MWL by SEC indicated that average molecular weights of heat treated milled wood lignin were lower than those of native milled wood lignin.

Modification of lignin by Geotrichum klebahnii.

13C-NMR spectroscopic analysis indicates that the yeast-like species Geotrichum klebahnii is an efficient microorganism for lignin biodegradation. This strain modified beechwood lignin even if it was the only carbon source by Cα-Cβ side chain cleavage, Cα-oxidations, aromatic ring cleavage and reductive reactions. The obtained results outline prospective application of G. klebahnii for biotechnological pre-treatment of lignocellulosic materials.

Release of mutagens after chemical or microbial degradation of beech wood lignin

The microbial or chemical degradation of lignin from untreated samples of beech wood dusts ( Fagus silvatica) resulted in the release of different mutagenic responses in the Salmonella/mammalian plate incorporation assay. In the first experiment using chemical degradation of lignin, dust samples were pre-extracted using acetone-water; the lignin portions were degraded into simpler compounds which were further fractionated on a Sephadex-LH20 column. The compounds isolated from the second phase of Sephadex, representing substances with a 3–4 ring structure and/or those of the same molecular weight, were highly mutagenic towards Salmonella typhimurium TA100 in the presence of metabolic activation. These substances were also active to some extent in strain TA 1537 both in the presence and absence of Aroclor-induced rat liver homogenates. In contrast, no direct- or indirect-acting mutagenicity was found when testing with strains TA97 and TA98. Strain TA1535 responded positively only to direct-acting mutagens in the fraction tested. The mutagenic fraction was found to be toxic to the cells when tested in a histidine-rich medium. Repurification of this mutagenic fraction, using silica-gel column chromatography, revealed much higher mutagenic activity than the test material towards strain TA100. In the second pilot experiment, Phanerochaete chrysosporium and Chaetomium globosum, which are known for their ability to degrade lignin, were each incubated with wood dusts in a mixture of physiological saline and nutrient broth for either 3 or 30 days. Significant mutagenic activity was observed with the dust extract after incubation with Ph. chrysosporium but not with Ch. globosum which is a known degrader of beech lignin. These results are discussed regarding hypotheses on the carcinogenicity of beech wood dusts.

A two-step composting process for woody resources

A novel process has been developed for converting woody resources into compost with high cation exchange capacity and humic acid content by two-step fermentation. The 1st step consists of lignin degradation with Coriolus versicolor, while the 2nd step is a general composting procedure. The influence of the degradation conditions (initial C/N ratio, temperature and moisture content) on the degradation of beech wood lignin by C. versicolor was studied in order to develop a composting process from woody resources. The lignin degradation rate, which was maximal with no added nitrogen source, was 23% and 31% after 4 weeks and 8 weeks of fermentation, respectively. The fulvic acid fraction increased as lignin degradation progressed, indicating that the precursor of humic acid was formed and accumulated as the result of lignin degradation. The cation exchange capacity and humic acid content of the compost after two-step fermentation reached 93 meq/100 g and 5.3%, respectively, as compared to 65 meq/100 g and 3.0%, respectively in fermentation using the 2nd step alone.