skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


This content will become publicly available on June 1, 2026

Title: Tailoring Polymer Properties Through Lignin Addition: A Recent Perspective on Lignin-Derived Polymer Modifications
Lignin, an abundant and renewable biopolymer, has gained significant attention as a sustainable modifier and building block in polymeric materials. Recent advancements highlight its potential to tailor mechanical, thermal, and barrier properties of polymers while offering a greener alternative to petroleum-based additives. This review provides an updated perspective on the incorporation of lignin into various polymer matrices, focusing on lignin modification techniques, structure–property relationships, and emerging applications. Special emphasis is given to recent innovations in lignin functionalization and its role in developing high-performance, biodegradable, and recyclable materials such as polyurethanes, epoxy resins, phenol-formaldehyde resins, lignin-modified composites, and lignin-based films, coatings, elastomers, and adhesives. These lignin-based materials are gaining attention for potential applications in construction, automated industries, packaging, textiles, wastewater treatment, footwear, supporting goods, automobiles, printing rollers, sealants, and binders.  more » « less
Award ID(s):
2203669
PAR ID:
10650104
Author(s) / Creator(s):
;
Publisher / Repository:
mdpi
Date Published:
Journal Name:
Molecules
Volume:
30
Issue:
11
ISSN:
1420-3049
Page Range / eLocation ID:
2455
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. null (Ed.)
    Lignin is the most abundant aromatic biopolymer and is the sustainable feedstock most likely to supplant petroleum-derived aromatics and downstream products. Rich in functional groups, lignin is largely peerless in its potential for chemical modification towards attaining target properties. Lignin’s crosslinked network structure can be exploited in composites to endow them with remarkable strength, as exemplified in timber and other structural elements of plants. Yet lignin may also be depolymerized, modified, or blended with other polymers. This review focuses on substituting petrochemicals with lignin derivatives, with a particular focus on applications more significant in terms of potential commercialization volume, including polyurethane, phenol-formaldehyde resins, lignin-based carbon fibers, and emergent melt-processable waste-derived materials. This review will illuminate advances from the last eight years in the prospective utilization of such lignin-derived products in a range of application such as adhesives, plastics, automotive components, construction materials, and composites. Particular technical issues associated with lignin processing and emerging alternatives for future developments are discussed. 
    more » « less
  2. Non-toxic resins formulated with renewable components have been receiving increased attention as sustainable alternatives to petroleum-based resins. In this work, we demonstrate a new class of lignin-amino acid (LA) resins, formulated with non-toxic components that are abundant and can be renewably sourced from field leftovers (corn cobs) and lysine (from bio-based sugars). NMR (1H, 31P, 13C-1H HSQC, 15N-1H HSQC, and 15N-1H HMBC), FTIR, thermogravimetric, gel permeation chromatography and elemental analyses provide insights into the physicochemical properties of the resins, including the presence of LA linkages such as C-N cross linking. The LA resin creates strong bonds between pieces of wood, metals (aluminum and stainless steel) and plastics. Internal bond strengths (IBS) of balsa wood and medium density fiberboard specimens glued with LA resins, measured using an Instron instrument, were comparable to those bonded with commercial polyurethane (PU) and polyvinyl acetate (PVAc) resins. Resins prepared with ozone-pretreated lignin have significantly larger molar masses and display increased bond strengths with glued substates as inferred from IBS measurements. This is attributed to the creation of reactive oxygen-based functionalities in the lignin upon ozone pretreatment. Lignin-amino acid resins thus show promise as a feasible and sustainable alternative to petroleum-based resins. 
    more » « less
  3. Epoxy is the most prevalent thermosetting resin in the field of polymer composite materials. There has been a growing interest in the development of bio-based epoxy resins as a sustainable alternative to conventional petrochemical epoxy resins. Advances in this field in recent years have included the use of various renewable resources, such as vegetable oils, lignin, and sugars, as direct precursors to produce bio-based epoxy resins. In the meantime, bio-oils have been produced via the decomposition of biomass through thermochemical conversion and mainly being used as renewable liquid fuels. It is noteworthy that bio-oils can be used as a sustainable resource to produce epoxy resins. This review addresses research progress in producing bio-oil-based epoxy resins from thermochemical processing techniques including organic solvent liquefaction, fast pyrolysis, and hydrothermal liquefaction. The production of bio-oil from thermochemical processing and its use to inject sustainability into epoxy resins are discussed. Herein, we intend to provide an overall picture of current attempts in the research area of bio-oil-based epoxy resins, reveal their potential for sustainable epoxy resins, and stimulate research interests in green/renewable materials. 
    more » « less
  4. null (Ed.)
    Fossil fuels are a cheap and abundant feedstock for polymeric materials that have enabled innumerable quality-of-life improvements. Yet, their declining supply and non-renewable nature have driven the pursuit of bio-based alternatives. Lignin represents the largest natural source of aromatic carbon on the planet, and thus, lignin-derived products have emerged as critical elements in the next generation of polymers. The relative abundance, large concentration of functional handles, and thermal stability of lignin make it an attractive target for bio-based polymers. However, the valorization of lignin to high-performance and cost-competitive materials remains a challenge. In this review, developments in the translation of lignin into value-added macromolecular components are discussed. Strategies to incorporate bulk lignin in polymer blends and composites are introduced with a focus on applications. Furthermore, recent advances in the preparation of higher-value thermoplastics, thermosets, and vitrimers from deconstructed lignin products are highlighted from a synthetic perspective. Finally, key hurdles and future opportunities in lignin valorization are explored. 
    more » « less
  5. Abstract Lignin is an aromatic‐rich biomass polymer that is cheap, abundant, and sustainable. However, its application in the solid electrolyte field is rare due to challenges in well‐defined polymer synthesis. Herein, the synthesis of lignin‐graft‐poly(ethylene glycol) (PEG) and its conductivity test for a solid electrolyte application are demonstrated. The main steps of synthesis include functionalization of natural lignin's hydroxyl to alkene, followed by graft‐copolymerization of PEG thiol to the lignin via photoredox thiol‐ene reaction. Two lignin‐graft‐PEGs are prepared having 22 wt% lignin (lignin‐graft‐PEG 550) and 34 wt% lignin (lignin‐graft‐PEG 2000). Then, new polymer electrolytes for conductivity tests are prepared via addition of lithium bis‐trifluoromethanesulfonimide. The polymer graft electrolytes exhibit ionic conductivity up to 1.4 × 10−4 S cm−1 at 35 °C. The presence of lignin moderately impacts conductivity at elevated temperature compared to homopolymer PEG. Furthermore, the ionic conductivity of lignin‐graft‐PEG at ambient temperature is significantly higher than homopolymer PEG precedents. 
    more » « less