Abstract Lignin, a widely available and renewable organic polymer, has several desirable properties and applications. However, as a by‐product of pulp and paper industry, it is mainly burned for energy. Limited understanding of the complex and heterogeneous structure and a shortage of tailored analysis methods hinder its utilization in higher value applications. This study describes and compares the use of two different static light scattering methods, laser diffraction and small‐angle light scattering (SALS), for studying lignin particle size in suspension. The results from laser diffraction showed that the selected particle concentration and absorption coefficient affect the measured sizes especially for particles <1 µm in diameter. For irregularly shaped particles with broad size distributions, sampling is the most important parameter affecting the results. SALS proved an efficient method for obtaining information on particle aggregation by providing primary particle sizes as well as aggregate sizes. Characterization of samples with spherical particles and narrow size distributions is straightforward with both laser diffraction and SALS, whereas the interpretation of results for more heterogeneous samples is less obvious. Static light scattering methods could make lignin particle size analysis more rapid and automated, thus enhancing lignin valorization, but should be applied carefully to avoid systematic errors.
Makkonen et al. (Sat,) studied this question.