Chlorination is one of the most applied technologies for drinking water disinfection. However, the generation of disinfection by-products (DBPs) in the chlorination process is threatening drinking water safety, especially when the concentration of natural organic matter (NOM) is high in source water. Climate change increases the fluc-tuation of NOM in source water, which further challenges water safety in small and rural communities. In this study, environmental microfluidics was introduced to a UVA-LED photocatalytic oxidation system for a rapid oxidation of NOM. The results showed that HA adsorption and degradation, and DOC degradation were more favored in low pH. At pH 5, 56.9% of HA and 58.1% of dissolved organic carbon (DOC) were removed in 3.4 min by the microreactor. DBP formation potential was efficiently reduced, with the highest reduction of THM and HAA formation potentials by 76% and 70.7%, respectively. Compared with the bottle reactor, the degradation rate constants of HA and DOC by UVA-LED microreactor were increased by 2.99 - 15.8 times, and 6.8 - 170.2 times, respectively. Homogenous irradiation and rapid mass transfer in the microreactor accelerated the inhibited oxidation of HA in acidic and base solutions and increased the apparent quantum yields of photo-catalysis. Further, the microfluidic photocatalytic oxidation was much more efficient in the reduction of DPBs formation potential in a source water sample. The process was rapid and had low chemical and energy con-sumption. Approaches on system scale-up, system simplification, and energy conservation would increase po-tential of microfluidic photocatalytic oxidation in water purification for households and small communities.