4.8 Article

Understanding lignin micro- and nanoparticte nucleation and growth in aqueous suspensions by solvent fractionation

Journal

GREEN CHEMISTRY
Volume 23, Issue 2, Pages 1001-1012

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0gc03632c

Keywords

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Funding

  1. USDA-NIFA [12513354]
  2. AFRI Competitive Grants Program: Sustainable Bioenergy and Bioproducts Challenge Area: Investing in America's Scientific Corps: Preparing a New Generation of Students, Faculty, and Workforce for Emerging Challenges in Bioenergy, Bioproducts, and the Bioeco [2017-67009-26771, A6131]

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Recent advances in developing sustainable, micro- and nanoscale materials from biobased resources have focused on utilizing lignin to strengthen the bioeconomy. However, there is a gap in the literature regarding the various interactions present during and after the formation of lignin micro- and nanoparticles (LPs). These interactions are influenced by the chemical composition, molecular weight distribution, and solvent/water polarity. Factors such as lignin concentration also play a role in nucleation and growth mechanisms, with LPs formed at low concentrations exhibiting larger particle sizes than those formed at higher concentrations.
In recent years, there have been many advances toward developing sustainable, micro- and nanoscale materials from biobased resources such as lignin aimed at strengthening the bioeconomy. It is critical to study the factors affecting nucleation and growth mechanisms, as well as the stability of lignin micro-and nanoparticles (LPs), to further enhance the development of such materials. However, there remains a gap in the literature examining the many interactions present during and after LP formation. These interactions vary with the chemical composition and molecular weight distribution of different kraft lignin (KL) fractions. To examine the composition of different lignin fractions, KL can be fractionated using water-miscible organic solvents of different polarities such as tetrahydrofuran (THF), acetone, and ethanol. Herein, we show that the micro- and nanoparticles formed from each lignin fraction exhibit significant differences in their size (50-300 nm), particle aggregation and fusion propensity, and spherical morphology in aqueous suspensions. These differences are proposed to be a result of the solvent lignin water interactions related to molecular weight and functional groups of the lignin fractions and solvent/water polarity. Another factor affecting the nucleation and growth of LPs is the lignin concentration. The LPs formed at low lignin concentrations exhibit a larger average particle size compared to the LPs formed at higher lignin concentrations due to the aggregation and fusion of the small particles. These results will allow for a stronger foundation in understanding the nucleation and growth of LPs when attempting to develop value-added applications for kraft lignin.

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