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This work describes the development of sulfated cellulose (SC) polymer and explores its potential as an electrolyte-membrane for direct methanol fuel cells (DMFC). The fabrication of our membranes was initiated by the preparation of the novel sulfated cellulose solution via controlled acid hydrolysis of microcrystalline cellulose (MCC). Ion-conductive crosslinked SC membranes were prepared following a chemical crosslinking reaction. SC solution was chemically crosslinked with glutaraldehyde (GA) and cured at 30 °C to produce the aforementioned membranes. Effects of GA concentration on methanol permeability, proton conductivity, water uptake and thermal stabilities were investigated. The crosslinking reaction is confirmed by FTIR technique where a bond between the primary OH groups of cellulose and the GA aldehyde groups was achieved, leading to the increased hydrophobic backbone domains in the membrane. The results show that the time of crosslinking reaction highly affects the proton conduction and methanol permeability. The proton conductivity and methanol crossover (3M) of our GA crosslinked SC membranes are 3.7 × 10−2 mS cm−1 and 8.2 × 10−9 cm2 s−1, respectively. Crosslinked sulfated cellulose films have lower ion conductivity than the state-of-the-art Nafion (10.2 mS cm−1); however, the methanol crossover is three orders of magnitude lower than Nafion membranes (1.0 × 10−5 cm2 s−1 at 1 M). Such biofilms with high methanol resistivity address the major hurdle that prevents the widespread applications of direct alcohol fuel cells.

A novel method of preparing skinned asymmetric membranes with two distinctive layers is described: a top layer composed of chemically cross‐linked polymer chains (dense layer) and a bottom layer of non‐cross‐linked polymer chains (porous substructure). The method consists of two simple steps that are compatible with industrial membrane fabrication facilities. Unlike conventional processes to prepare asymmetric membranes, with this approach it is possible to finely control the structure and functionalities of the final membrane. The thickness of the dense layer can be easily controlled over several orders of magnitude and targeted functional groups can be readily incorporated in it.

Crosslinked polythiosemicarbazide (PTSC) membranes with a positively charged surface are fabricated via a reaction with (3‐glycidyloxypropyl)trimethoxysilane. The integrally asymmetric ultrafiltration membranes discussed here can be easily prepared by water‐induced phase separation using a PTSC solution in dimethylsulfoxide (DMSO). The crosslinked PTSC membranes are stable in DMSO, N,N‐dimethylformamide, and tetrahydrofuran and they reject molecules of molecular weights (MW) above 1300 g mol−1. The influence of the crosslinking agent on the surface charge, membrane solvent resistance, and membrane performance is discussed. The crosslinked asymmetric PTSC membranes totally reject Direct Red dye (MW 1373 g mol−1), while the pristine PTSC membrane does not show any rejection for this dye. This finding suggests that an inorganic‐type‐network is formed during the crosslinking reaction, which tunes the pore size of the prepared membranes.

Light‐management films made entirely from natural polymers with tunable haze properties are developed via a facile approach. A novel green method based simply on the blending of network cellulose (NC)/water suspension with alginate (CaAlg) aqueous solution is proposed. The unique NC suspension created by a controlled hydrolysis of microcrystalline cellulose acts as the scatterer media while alginate serves as the transparent host matrix. NC features isotropic intertwined network of nanofibers that contributes to light scattering and produces optical haze. The opaque but hazy NC is dispersed purposefully in the alginate film, where its original properties are preserved owing to its poor solubility in water. Additionally, the dispersion notably increases the roughness of the composite film surface and acts as a light scatterer. Eventually, composite CaAlg/NC film with high transparency (>94%) and customized haze (15–73%) at 550 cm−1 wavelength is fabricated. Herein, the transparent alginate is successfully combined with the hazy cellulose of uniformly distributed nanofibers by blending to fabricate transparent/hazy all‐natural films. The fabricated films exhibit high transparency with tailored transmission haze. The film is highly fitting for large‐scale production and adequate to meet different haze requirements to accommodate different applications such as privacy protection films and antiglare/antireflection coatings.