Abstract

The complexity of lignin and hemicellulose segmentation has been known since the middle of the ninetieth century. Studies confirmed that all lignin units in coniferous species and 47–66% of lignin moieties in deciduous species are bound to hemicelluloses or cellulose molecules in lignin–carbohydrate complexes (LCC). Different types and proportions of lignin and polysaccharides present in biomass lead to the formation of LCC with a great variety of compositions and structures. The nature and amount of LCC linkages and lignin substructures affect the efficiency of pulping, hydrolysis, and digestibility of biomass. This review paper discusses the structures, compositions, and properties of LCC present in biomass and in the products obtained via pretreating biomass. Methods for extracting, fractionating, and analyzing LCC of biomass, pulp, and spent pulping liquors are critically reviewed. The main perspectives and challenges associated with these technologies are extensively discussed. LCC could be extracted from biomass following varied methods, among which dimethyl sulfoxide or dioxane (Björkman’s) and acetic acid (LCC-AcOH) processes are the most widely applied. The oxidation and methylation treatments of LCC materials elucidate the locations and frequency of binding sites of hemicelluloses to lignin. The two-dimensional nuclear magnetic resonance analysis allows the identification of the structure and the quantity of lignin–carbohydrate bonds involved in LCC. LCC application seems promising in medicine due to its high anti-HIV, anti-herpes, and anti-microbial activity. In addition, LCC was successfully employed as a precursor for the preparation of spherical biocarriers.

Highlights

  • Biomass shows great potential for fuel and non-fuel applications

  • selective index (SI) is defined as the ratio of two parameters: 50% cytotoxic concentration (­CC50), which is defined as the amount of the compound required for the reduction of the number of living cells by 50%, and 50% effective concentration ­(EC50) that raises the viability of UV-irradiated cells by 50% [105, 106]

  • The compositions, structures, and properties of lignin–carbohydrate complexes (LCC) presented and extracted from different biomass sources are described in this review paper

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Summary

Background

Biomass shows great potential for fuel and non-fuel applications. It is a mixture of cellulose, hemicellulose, lignin, and extractives [1], which are considered as the most common natural polymers on earth [2]. Bioconversion procedures can be applied for separating cellulosic sugars from biomass These methods are based on the liberation of the bonds of lignin and holocellulose. LCC linkage plays a crucial role in wood structure, since all lignin moieties in softwoods [19] and 47–66% of lignin fragments in hardwoods [20] are bound to carbohydrates, mainly to hemicellulose [21]. A low yield of kraft pulping process is related to the challenge in breaking lignin–carbohydrate linkages in hardwood species [27], which can be attributed to the alkaline stability of LCC bonds. Jin et al [54] report that over 50% of lignin units in softwoods and 17% in hardwoods are covalently (molecularly) bound to cellulose moieties in wood. It has been found that high amounts of ferulate and coumarate acids are bound to a OH b

OH OH
ND ND
LCC source
Supernatant MWL
Dissolution Solution
Extraction Residue
Precipitation Residue
HCl pH adjustment
Drying Residue
Smith degraded LCC
Methylated LCC
Phenyl glycosidic
LCC application
Conclusions
Findings
List of symbols

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