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Particle-stabilized bicontinuous emulsions (bijels) are made of two interwoven liquid channel systems. In contrast to emulsion droplets, the liquid-liquid interface of bijels curves both towards the oil and the water phases. Thus, particles with equal wettability for both oil and water are needed to stabilize the interface. In this research paper, we enhance the understanding of nanoparticle functionalization by a surfactant for controlling the particle wettability. To this end, we develop a novel, single-channel, continuous flow method, enabling the rapid synthesis and analysis of bijels formed via solvent transfer induced phase separation (STrIPS). Silica nanoparticles are functionalized with the positively charged surfactant (cetyltrimethylammonium+, CTA+). Zeta-potential and colloidal stability analysis are employed to characterize the CTA+ functionalization. Confocal and electron microscopy are used to visualize the resulting bijel structures. Bijels with nearly uniform, sub-micrometer channels are obtained when the particle functionalization by CTA+ is regulated. To this end, the initial negative zeta-potential of the particles needs to be low enough to prevent excessive CTA+ adsorption. The adsorption is further controlled by adjusting the concentrations of CTA+, salt and glycerol additive. This report shows that the nanoparticle surfactant modification depends on multiple parameters, providing guidance for future bijel synthesis approaches. [Display omitted] • Improved control over fabrication of nanoparticle stabilized bicontinuous emulsions (bijels). • Development of a single channel flow device for the fabrication of bijels. • Influence of aluminum content in silica nanoparticles on bijel fabrication. • Control of nanoparticle interfacial behavior during bijel formation. • Printing of bijel fibers enables potential applications in liquid-liquid extraction and reactive separations. [ABSTRACT FROM AUTHOR]