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A study on the physical and mechanical properties of beeswax (BW), candelilla wax (CW), paraffin wax (PW) and blends was carried out with the aim to evaluate their usefulness as coatings for cheeses. Waxes were analyzed by X-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), differential scanning calorimetry (DSC), permeability, viscosity, flexural and tensile tests and scanning electron microscopy. Cheeses were coated with the waxes and stored for 5 weeks at 30 °C. Measured parameters were weight, moisture, occurrence and degree of fractures, and dimensional changes. The crystal phases identified by XRD for the three waxes allowed them to determine the length of alkanes and the nonlinear compounds in crystallizable forms in waxes. FTIR spectra showed absorption bands between 1800 and 800 cm−1 related to carbonyls in BW and CW. In DSC, the onset of melting temperature was 45.5 °C for BW, and >54 °C for CW and PW. Cheeses coated with BW did not show cracks after storage. Cheeses coated with CW and PW showed microcraks, and lost weight, moisture and shrunk. In the flexural and tensile tests, BW was ductile; CW and PW were brittle. BW blends with CW or PW displays a semi ductile behavior. Cheeses coated with BW blends lost less than 5% weight during storage. The best waxes were BW and the blends.

Nanographene oxide (nGO) flakes—graphene oxide with a lateral size of ≈100 nm or less—hold great promise for superior flux and energy‐efficient nanofiltration membranes for desalination and precise ionic sieving owing to their unique high‐density water channels with less tortuousness. However, their potential usage is currently limited by several challenges, including the tricky self‐assembly of nano‐sized flakes on substrates with micron‐sized pores, severe swelling in aqueous solutions, and mechanical instability. Herein, the successful fabrication of a robust membrane stacked with nGO flakes on a substrate with a pore size of 0.22 µm by vacuum filtration is reported. This membrane achieved an unprecedented water permeance above 819.1 LMH bar−1, with a high rejection rate of 99.7% for multivalent metal ions. The nGO flakes prepared using an electron beam irradiation method, have uniquely pure hydroxyl groups and abundant aromatic regions. The calculations revealed the strong hydrogen bonds between two nGO flakes, which arise from hydroxyl groups, coupled with hydrophobic aromatic regions, greatly enhance the stability of stacked flakes in aqueous solutions and increase their effective lateral size. The research presents a simple yet effective approach toward the fabrication of advanced 2D nanographene membranes with superior performance for ion sieving applications. A simple yet effective approach toward the fabrication of nanographene oxide (nGO) membranes with superior performance for ion sieving is developed in this work.

This work was funded by grant AGL2015-64235-R from the Plan Nacional de I+D, Ministry of Education and Science, Spain. CD is the recipient of a predoctoral scholarship granted by the Universitat de Lleida. PH-L was recipient of a PhD scholarship from Zespri™ International. HH was supported by an Oversea Study Program, Guangzhou Elite Project, China.

A passive regulation system for the water content has been developed and evaluated for a proton exchange membrane fuel cell. It is of particular relevance for micro-fuel cells, whose volume, weight and extra-consumption of fuel and power for subsidiary components must be kept to a minimum. This solution consists of a self-regulating humidity system implemented at the anode chamber that allows free water exchange with the environment through the surface of a gas-tight membrane. The micro-fuel cell, which is designed according to the patent WO2015025070A1, has been assembled and operated under completely passive conditions. The behavior of the anode humidity regulation system has been analyzed externally and in situ. The external part of the anode, where the humidity exchange with the environment takes place, has been isolated in a closed chamber and a hygrometer has been used to register the relative humidity in the zone near to the water exchange film. The results obtained from the operation of this innovative system are discussed in the light of the water permeation behavior of different Nafion membranes.

Neat poly(vinylidene fluoride) (PVDF) ultrafiltration (UF) membranes exhibit poor water permeance and surface hydrophobicity, resulting in poor antifouling properties. Herein, we report the synthesis of a fluorine-containing amphiphilic graft copolymer, poly(2,2,2-trifluoroethyl methacrylate)-g-poly(ethylene glycol) behenyl ether methacrylate (PTFEMA-g-PEGBEM), hereafter referred to as PTF, and its effect on the structure, morphology, and properties of PVDF membranes. The PTF graft copolymer formed a self-assembled nanostructure with a size of 7–8 nm, benefiting from its amphiphilic nature and microphase separation ability. During the nonsolvent-induced phase separation (NIPS) process, the hydrophilic PEGBEM chains were preferentially oriented towards the membrane surface, whereas the superhydrophobic PTFEMA chains were confined in the hydrophobic PVDF matrix. The PTF graft copolymer not only increased the pore size and porosity but also significantly improved the surface hydrophilicity, flux recovery ratio (FRR), and antifouling properties of the membrane. The membrane performance was optimal at 5 wt.% PTF loading, with a water permeance of 45 L m−2 h−1 bar−1, a BSA rejection of 98.6%, and an FRR of 83.0%, which were much greater than those of the neat PVDF membrane. Notably, the tensile strength of the membrane reached 6.34 MPa, which indicated much better mechanical properties than those reported in the literature. These results highlight the effectiveness of surface modification via the rational design of polymer additives and the precise adjustment of the components for preparing membranes with high performance and excellent mechanical properties.

Two‐dimensional (2D) nanochannels have demonstrated outstanding performance for sieving specific molecules or ions, owing to their uniform molecular channel sizes and interlayer physical/chemical properties. However, controllably tuning nanochannel spaces with specific sizes and simultaneously achieving high mechanical strength remain the main challenges. In this work, the inter‐sheet gallery d‐spacing of graphene oxide (GO) membrane is successfully tailored with high mechanical strength via a general radical‐induced polymerization strategy. The introduced amide groups from N‐Vinylformamide significantly reinforce the 2D nanochannels within the freestanding membranes, resulting in an ultrahigh tensile strength of up to 105 MPa. The d‐spacing of the membrane is controllably tuned within a range of 0.799–1.410 nm, resulting in a variable water permeance of up to 218 L m−2 h−1 bar−1 (1304% higher than that of the pristine GO membranes). In particular, the tailored membranes demonstrate excellent water permeance stability (140 L m−2 h−1 bar−1) in a 200‐h long‐term operation and high selectivity of solutes under harsh conditions, including a wide range of pH from 4.0 to 10.0, up to a loading pressure of 12 bar and an external temperature of 40 °C. This approach comprehensively achieves a balance between sieving performance and mechanical strength, satisfying the requirements for the next‐generation molecular sieving membranes. A general radical‐induced polymerization strategy to synthesize poly(N‐vinylformamide) short chains on GO nanosheets to tailor the gallery space of 2D nanochannels and build robust hydrogen‐bonded frameworks that help boost water permeance and reinforce the mechanical strength of the membranes.

Reducing the specific energy consumption of reverse osmosis (RO) processes motivates the development of new membrane materials that have enhanced water permeability while maintaining low salt permeability (high rejection). Nanocomposite membranes have shown great promise in achieving these goals, particularly those using nanotubes as fillers. Here, we report on the relationships between the orientations and surface functionalities of imogolite nanotubes (INTs) with water and salt permeabilities for polyamide nanocomposite membranes. An external electric field was used to manipulate the INT orientation within the polyamide active layer. The INT interior and exterior chemistries, respectively, were made hydrophobic using methyl triethoxysilane as a precursor during INT synthesis and post-synthesis modification with alkali-phosphate groups. Irrespective of nanotube orientation or surface chemistry, membrane permeance increased from 0.3 to ≥1.0 L m−2 h−1 bar−1. A salt permeability comparable to the conventional polyamide membrane was maintained by making the INT pore throat hydrophobic. These findings indicated that salt rejection could be tailored by manipulating the INT interior surface chemistry without sacrificing water permeability.

The adhesion enhancement of a graphene oxide (GO) layer on porous ceramic substrates is a crucial step towards developing a high-performance membrane for many applications. In this work, we have achieved the chemical anchoring of GO layers on custom-made macroporous disks, fabricated in the lab by pressing α-Al2O3 powder. To this end, three different linkers, polydopamine (PDA), 3-Glycidoxypropyltrimethoxysilane (GPTMS) and (3-Aminopropyl) triethoxysilane (APTMS), were elaborated for their capacity to tightly bind the GO laminate on the ceramic membrane surface. The same procedure was replicated on cylindrical porous commercial ZrO2 substrates because of their potentiality for applications on a large scale. The gas permeance properties of the membranes were studied using helium at 25 °C as a probe molecule and further scrutinized in conjunction with water permeance results. Measurements with helium at 25 °C were chosen to avoid gas adsorption and surface diffusion mechanisms. This approach allowed us to draw conclusions on the deposition morphology of the GO sheets on the ceramic support, the mode of chemical bonding with the linker and the stability of the deposited GO laminate. Specifically, considering that He permeance is mostly affected by the pore structural characteristics, an estimation was initially made of the relative change in the pore size of the developed membranes compared to the bare substrate. This was achieved by interpreting the results via the Knudsen equation, which describes the gas permeance as being analogous to the third power of the pore radius. Subsequently, the calculated relative change in the pore size was inserted into the Hagen–Poiseuille equation to predict the respective water permeance ratio of the GO membranes to the bare substrate. The reason that the experimental water permeance values may deviate from the predicted ones is related to the different surface chemistry, i.e., the hydrophilicity or hydrophobicity that the composite membranes acquire after the chemical modification. Various characterization techniques were applied to study the morphological and physicochemical properties of the materials, like FESEM, XRD, DLS and Contact Angle.

Cuticular wax is a hydrophobic barrier between the plant surface and the environment that effectively reduces the loss of water. The surface of Welsh onion leaves is covered with wax. To explain the relationship between wax composition and water loss, we conducted this experiment. The water permeability and wax composition of leaves were determined by chemical and GC-MS methods. We performed a comparative analysis of the differences between the two cultivars and analyzed the relationship between water permeability and waxy components. Overall, the permeability to water was higher in ‘Zhangqiu’ than in ‘Tenko’. The wax amount of ‘Tenko’ was 1.28-fold higher than that of ‘Zhangqiu’ and was primarily explained by the much larger amounts of ketones and alcohols in the former. Among the waxy components, C29 ketones were most abundant. There were substantial discrepancies in wax composition, total wax content, and water permeability between the two cultivars. The main reason for the discrepancy in water permeability may be the significantly lower aliphatic fraction in ‘Zhangqiu’ than in ‘Tenko’. This study makes a vital contribution to drought resistance research on allium plants.

• During harvest, fleshy berry tomato fruits (Solanum lycopersicum) were wounded at their stem scar. Within 3 d, this wound was rapidly sealed by a process covering the wound site with a membranous layer which effectively protects the tomato fruit from excessive water loss, nutrient elution and the entry of pathogens. • Chemical analysis of the de novo synthesized stem scar tissue revealed the presence of aromatic and aliphatic components characteristic of the biopolyester suberin. • Gene expression patterns associated with suberization were identified at the stem scar region. Changes in the relative abundance of different transcripts suggested a potential involvement of the plant hormone abscisic acid (ABA) in the wound‐healing processes. • The amount of ABA present in the stem scar tissue showed a significantly increased level during wound healing, whereas ABA‐deficient mutants notabilis, flacca and sitiens were largely devoid of this rise in ABA levels. The mutant fruits showed a retarded and less efficient suberization response at the stem scar wound, whereas the rate and strength of this response were positively correlated with ABA content. These results clearly indicate in vivo the involvement of ABA in the suberization‐based wound‐healing processes at the stem scar tissue of tomato fruits.