Kraft lignin (KL) was treated by employing mild oxidation conditions enhanced by ultrasound irradiation (US) for obtaining more functionalized particles, avoiding the undesired side reactions of degradation and depolymerization. The aim was to obtain products with plausible value for applications with a greater potential market, enabling the introduction of low-cost bio-based materials for technically advanced applications. In the present work, KL was oxidized in alkaline media, applying low temperatures (30-60 °C), short times (15 to 60 min), and US waves (20 kHz). The influence of incorporating hydrogen peroxide (H 2 O 2) as an oxidizing agent was also studied, as well as the chemical composition, physicochemical, thermal, and morphological properties of the final lignin particles. It was observed from Quantitative Acid Hydrolysis (QAH), Elemental Analysis (EA), and molecular weights (M w) that oxidized lignin particles (OxL) did not suffer any major degradation. Other techniques used to determine physicochemical properties, such as Fourier Transformed Infrared (FTIR), 31 Phosphorous Nuclear Magnetic Resonance (31 P NMR), or Ultraviolet-visible (UV-vis) methods, corroborated oxidation reactions, evident by the increment of carboxylic groups. The most noticeable difference, however, was observed when the stability and morphology of the particles were observed by Dynamic Light Scattering (DLS) and Transmission Electron Microscopy (TEM). Some conditions greatly promoted the formation of more stable and nanosized particles. The best conditions were the mildest but with the highest reaction times (no addition of H 2 O 2 , 30 °C and 60 minutes). Moreover, all reactions had good recovery yields, above 70% of the original lignin.