Increased demand for highly selective and energy-efficient separations processes has stimulated substantial interest in emerging two-dimensional (2D) nanomaterials as a potential platform for next-generation membranes. However, persistently poor separation performance continues to hinder the viability of many novel 2D-nanosheet membranes in desalination applications. In this study, we examine the role of the lamellar structure of 2D membranes on their performance. Using self-fabricated molybdenum disulfide (MoS2) membranes as a platform, we show that the separation layer of 2D nanosheet frameworks not only fails to demonstrate water-salt selectivity but also exhibits low rejection toward dye molecules. Moreover, the MoS2 membranes possess a molecular weight cutoff comparable to its underlying porous support, implying negligible selectivity of the MoS2 layer. By tuning the nanochannel size through intercalation with amphiphilic molecules and analyzing mass transport in the lamellar structure using Monte Carlo simulations, we reveal that small imperfections in the stacking of MoS2 nanosheets result in the formation of catastrophic microporous defects. These defects lead to a precipitous reduction in the selectivity of the lamellar structure by negating the interlayer sieving mechanism that prevents the passage of large penetrants. Notably, the imperfect stacking of nanosheets in the MoS2 membrane was further verified using 2D X-ray diffraction measurements. We conclude that developing a well-controlled fabrication process, in which the lamellar structure can be carefully tuned, is critical to achieving defect-free and highly selective 2D desalination membranes.
Surface functionalization using two-dimensional (2D) graphene oxide (GO) materials is a promising technique to enhance the biofouling resistance of membranes used in water purification and reuse. However, the role of GO exposure, which is crucial for the contact-mediated toxicity mechanism, has not been well evaluated or elucidated in previous studies. Herein, we employ bioinspired polydopamine chemistry to fabricate GO-functionalized membranes through two strategies: coating and blending. The two types of GO-functionalized membranes displayed comparable roughness, hydrophilicity, water permeability, and solute retention properties but different degrees of GO nanosheet exposure on the membrane surface. When in contact with the model bacterium, Escherichia coli, the GO-coated membrane exhibited enhanced biofouling resistance compared to that of the GO-blended membrane, as evidenced by lower viable cells in static adsorption experiments, and lower water flux decline and higher flux recovery in dynamic biofouling experiments. Moreover, the development of biofilm on the GO-coated membrane was also inhibited to a greater extent than on the GO-blended membrane. Taken together, our findings indicate the paramount importance of GO exposure on the membrane surface in conferring antibacterial activity and biofouling resistance, which should be considered in the future design of antibiofouling membranes using 2D nanomaterials.
Surface modification with bactericides is a promising approach to imparting membrane materials with biofouling resistance. However, chemical modification of membranes made from inert materials, such as polyvinylidene fluoride (PVDF) and polysulfone, is challenging because of the absence of reactive functional groups on these materials. In this study, we develop a facile procedure using benzophenone as an anchor to graft biocidal graphene oxide (GO) to chemically inactive membrane materials. GO nanosheets are first functionalized with benzophenone through an amide coupling reaction. Then, benzophenone-functionalized GO nanosheets are irreversibly grafted to the inert membrane surfaces via benzophenone-initiated cross-linking under ultraviolet irradiation. The binding of GO to the membrane surface is confirmed by scanning electron microscopy and Raman spectroscopy. When exposed to a model bacterium (Escherichia coli), GO-functionalized PVDF and polysulfone membranes exhibit strong antibacterial activity, reducing the number of viable cells by 90% and 75%, respectively, compared to the number with the pristine membranes. Notably, this bactericidal effect is imparted to the membranes without compromising membrane permeability or solute retention properties. Our results highlight the potential application of benzophenone chemistry in membrane surface modification as well as its promise in developing antimicrobial surfaces for a variety of environmental applications.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.