The low gas-to-liquid mass transfer rate is one of the main challenges in syngas biomethanation. In this work, a new concept of the floating membrane system with high gas hold-up was introduced in order to enhance the mass transfer rate of the process. In addition, the effect of the inoculum-to-syngas ratio was investigated. The experiments were conducted at 55 °C with an anaerobic mixed culture in both batch and continuous modes. According to the results from the continuous experiments, the H2 and CO conversion rates in the floating membrane bioreactor were approximately 38% and 28% higher in comparison to the free (suspended) cell bioreactors. The doubling of the thickness of the membrane bed resulted in an increase of the conversion rates of H2 and CO by approximately 6% and 12%, respectively. The highest H2 and CO consumption rates and CH4 production rate recorded were approximately 22 mmol/(L·d), 50 mmol/(L·d), and 34.41 mmol/(L·d), respectively, obtained at the highest inoculum-to-syngas ratio of 0.2 g/mL. To conclude, the use of the floating membrane system enhanced the syngas biomethanation rates, while a thicker membrane bed resulted in even higher syngas conversion rates. Moreover, the increase of the inoculum-to-syngas ratio of up to 0.2 g/mL favored the syngas conversion.
Biofouling remains a critical challenge in thin-film composite reverse osmosis (TFC-RO) membranes, leading to severe flux decline during long-term operation. This study presents a comparative evaluation of unmodified and CuO-enhanced TFC-RO membranes immobilized with a partially purified lactonase (PPL) enzyme as a quorum-quenching strategy. TFC-RO membranes were fabricated via interfacial polymerization using optimized 18 wt% PES supports, and CuO nanoparticles (0.01 wt%) were incorporated into the polyamide layer to improve surface properties. The PPL enzyme from Bacillus sp. T5 exhibited optimal activity at 25 °C and pH 7 and was immobilized with efficiencies of 86.0% and 90.2% for unmodified and CuO-enhanced membranes, respectively. CuO incorporation reduced the contact angle from 75.8° to 59.7° and decreased surface roughness by ~38–39%, while maintaining high salt rejection (~97%). Under low-pressure operation, CuO-enhanced membranes showed improved water permeability. Biofouling tests using Escherichia coli revealed lower flux decline for enzyme-immobilized membranes (42.6%) compared to unmodified membranes (51.6%). Notably, CuO-enhanced biocatalytic membranes exhibited the most stable performance, maintaining a post-biofouling flux of ~5.6 L m⁻² h⁻¹ and a salt rejection of 95.1%. SEM, FTIR, and confocal microscopy confirmed reduced biofilm coverage and more homogeneous surface morphology. Overall, this study demonstrates that combining CuO nanoparticles with immobilized PPL enzyme offers an effective dual-function antifouling strategy for TFC-RO membranes.