As part of my thesis, I prepared lignin nanoparticles (LNPs) from two types of lignin: organosolv and kraft lignin. I compared the LNPs prepared from organosolv lignin based on differences in their preparation methods. IR spectral analysis revealed that the nanoparticle structure remains unchanged regardless of the starting lignin sample; only a reduction in peak intensity was observed. There were no significant differences between the spectra of LNPs prepared with acetone (LNP-A) and those prepared with ethanol (LNP-E). Hydrodynamic diameter analysis showed particle sizes ranging from several hundred to several thousand nanometers, with irregular shapes. The diameters of LNP-E particles were significantly larger than those of LNP-A, and SEM image analysis indicated that they formed larger agglomerates. Zeta-potential measurements also suggested agglomerate formation, as the value was less negative for LNP-E than for LNP-A. For further analysis, I used only the LNPs prepared with acetone, as they were produced using the original procedure.
In the second part of the thesis, I analyzed the binding of lignin nanoparticles (LNPs) and the herbicide 2,4-D. To compare the LNPs prepared via the anti-solvent precipitation method (LNP-A), I used LNPs prepared via the sodium p-toluenesulfonate precipitation method (LNP-K). Binding between the nanoparticles and the herbicide was successful for both LNP samples. The mass of bound herbicide was very similar for both samples, though slightly higher for the LNP-A sample. The results showed no significant difference in the mass of bound 2,4-D based on the extraction method used to recover it from the mixture.
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