Search Results (194)

Bio-nanocomposites based on poly (vinyl alcohol) (PVA) and cellulosic nanostructures are favorable for active food packaging applications. The current study systematically investigates the mechanical properties, gas permeation, and swelling parameters of PVA composites with cellulose nanocrystals (CNC) or nano lignocellulose (NLC) fibers. Alterations in these macroscopic properties, which are critical for food packaging applications, are correlated with structural information at the molecular level. Strong interactions between the fillers and polymer host matrix were observed, while the PVA crystallinity exhibited a maximum at ~1% loading. Finally, the orientation of the PVA nanocrystals in the uniaxially stretched samples was found to depend non-monotonically on the CNC loading and draw ratio. Concerning the macroscopic properties of the composites, the swelling properties were reduced for the D1 food simulant, while for water, a considerable decrease was observed only when high NLC loadings were involved. Furthermore, although the water vapor transmission rates are roughly similar for all samples, the CO₂, N₂, and O₂ gas permeabilities are low, exhibiting further decrease in the 1% and 1–5% loading for CNC and NLC composites, respectively. The mechanical properties were considerably altered as a consequence of the good dispersion of the filler, increased crystallinity of the polymer matrix, and morphology of the filler. Thus, up to ~50%/~170% enhancement of the Young’s modulus and up to ~20%/~50% enhancement of the tensile strength are observed for the CNC/NLC composites. Interestingly, the elongation at break is also increased by ~20% for CNC composites, while it is reduced by ~40% for the NLC composites, signifying the favorable/unfavorable interactions of cellulose/lignin with the matrix. Full article

This present study covers a complex approach to study a hybrid separation technique: membrane-assisted gas absorption for CO₂ capture from flue gases. It includes not only the engineering aspects of the process, particularly the cell design, flow organization, and process conditions, but also a complex study of the materials. It covers the spinning of hollow fibers with specific properties that provide sufficient mass transfer for their implementation in the hybrid membrane-assisted gas absorption technique and the design of an absorbent with a new ionic liquid—bis(2-hydroxyethyl) dimethylammonium glycinate, which allows the selective capture of carbon dioxide. In addition, the obtained hollow fibers are characterized not only by single gas permeation but with regard to mixed gases, including the transfer of water vapors. A quasi-real flue gas, which consists of nitrogen, oxygen, carbon dioxide, and water vapors, is used to evaluate the separation efficiency of the proposed membrane-assisted gas absorption technique and to determine its ultimate performance in terms of the CO₂ content in the product flow and recovery rate. As a result of this study, it is found that highly permeable fibers in combination with the obtained absorbent provide sufficient separation and their implementation is preferable compared to a selective but much less permeable membrane. Full article

Water electrolysis (WE) is a green technology for producing hydrogen gas without the emission of carbon dioxide. The ideal membrane materials in WE should be capable of transporting ions quickly and have gas barrier properties in harsh work environments. However, currently, no desirable measurement method has been developed for evaluating the gas barrier behavior of the membranes. Hence, an in-situ electrochemical method is developed to measure the gas permeability of membranes in the actual electrolysis environment, with the supersaturated state of H₂ in the electrolyte and H₂ bubbles during the electrolysis process. Four membranes, including Zirfon (a state-of-the-art alkaline WE membrane), polyphenylene sulfide fabric (PPS, a commercial alkaline WE membrane), FAA-3-PK-75 (a commercial anion-exchange membrane), and BILP-PE (a home-made composite membrane) were employed as the standard samples to perform the electrochemical measurement under different current densities, temperatures, and electrolyte concentrations. The results show that an increase in electrolytic current density or temperature or a decrease in KOH concentration can increase the H₂ permeability of the membrane. The two porous membranes, Zirfon and PPS, are more affected by the current density and KOH concentration, while the dense FAA-3-PK-75 and BILP-PE membranes have a stronger ability to hinder H₂ permeation. Under the conditions of 80 °C, 30 wt.% KOH, 101 kPa, and 400 mA·cm⁻², the hydrogen permeability (×10¹⁰ L·cm·cm⁻²·s⁻¹) of Zirfon, PPS, FAA, and BILP-PE are 263, 367, 28.3, and 5.32, respectively. Full article

This paper presents novel soluble (co)poly(hydroxyimide)s ((co)PIOH) based on 4,4′-oxydiphthalic anhydride (ODPA), 3,3′-dihydroxybenzidine (HAB), and 3,6-diaminodurene (D) with the 3/1, 1/1, and 1/3 HAB/D ratios. This chemical structure of the compounds provides the possibility of their future modification through the thermal rearrangement (polybenzoxazoles) or functionalization via Mitsunobu reaction (azo side-chain polyimides), i.e., obtaining new materials with interesting properties and therefore with expanded applications. Copolymers were characterized via FTIR, NMR, XRD, and GPC methods to confirm their structure, composition, and molar masses. The effect of copolymer composition on the thermal, mechanical, optical, and permeation properties studied for He, O₂, N₂, and CO₂, as well as hydrophobicity, was investigated. They exhibited a large interval between the glass transition temperature and the decomposition temperature, making them promising for the thermoforming technique. Transmittance above 90% was noted in the visible range for all (co)PIOH films deposited on a glass substrate. Young’s modulus of fabricated membranes was in the range of 2.37 to 3.38 GPa. The highest permeability coefficients were recorded for (co)PIOH with a 1:3 HAB-to D-ratio. Full article

The purpose of this study is to evaluate the strength of polyamide utilized in high pressure hydrogen transmission, exemplified by reinforced plastic hoses. The research encompasses a comprehensive investigation of materials employed in hydrogen infrastructure, focusing on their barrier and mechanical properties. It addresses challenges associated with hydrogen storage and transport, presenting various types of tanks and hoses commonly used in the industry and detailing the materials used in their construction, such as metals and polymers. Two materials were analyzed in the study; one new material and one material exposed to hydrogen. Key mechanisms and factors affecting gas permeation in materials are discussed, including an analysis of parameters such as fractional free volume (FFV), solubility coefficient (S), diffusion coefficient, and permeability coefficient. Methods for evaluating material permeation were outlined, as they are essential for assessing suitability in hydrogen infrastructure. Experimental analyses included Fourier Transform Infrared Spectroscopy (ATR), differential thermal analysis (DTA), scanning electron microscopy (SEM), and Energy dispersive X-ray spectroscopy (EDS). These techniques provided detailed insights into the structure and properties of polyamide, allowing for an assessment of its performance under high pressure hydrogen conditions. Pressure was identified as a critical factor influencing both the material’s mechanical strength and its hydrogen transport capability, as it affects the quantity of adsorbed particles. According to the DTA investigation, the polyamide demonstrates minimal mass loss at lower temperatures, indicating a low risk of material degradation. However, its performance declines significantly at higher temperatures (above 350 °C). Up to 250 °C, the material shows no notable decomposition occurred, suggesting its suitability for certain applications. The presence of functional groups was found to play a significant role in gas permeation, highlighting the importance of detailed physicochemical analysis. XRD studies revealed that hydrogen exposure did not significantly alter the internal structure of polyamide. These findings suggest that the structure of polyamide is well-suited for operation under specific conditions, making it a promising candidate for use in hydrogen infrastructure. However, the study also highlights areas where further research and optimization are needed. Overall, this work provides valuable insights into the properties of polyamide and its potential applications in hydrogen systems. Full article

Hydrogen became one of the most studied energy carriers after the global energy crisis and can replace gas and oil as clean fuels. The main challenge is its safe storage and long-distance transportation: steel is among the materials most used for hydrogen storage and transportation. However, steel is susceptible to hydrogen embrittlement (HE). HE can be prevented by depositing hydrogen barrier coatings on the steel surface. This review provides an overview of the hydrogen permeation mechanism and the analytical methods employed to evaluate the performance of the hydrogen permeation barriers. The focus is on Ni and electroless Ni-P coatings deposited on steel as hydrogen barriers. These coatings have been used so far for their anti-corrosion and wear properties; they are currently of interest due to their low hydrogen permeability. The simplicity of production and the possibility of achieving a homogeneous coating, regardless of the geometry of the substrate, make the electroless deposition process of the Ni-P alloy a candidate for ‘in situ’ applications in existing pipelines. This process can be implemented by using and adapting the established pig batch technology. Full article

The exponential increase in medical waste production has increased the difficulty of waste management, resulting in higher medical waste dispersion into the environment. By employing a circular economy approach, it is possible to develop new materials by waste valorization. The employment of biodegradable and renewable agro-food, waste-derived materials may reduce the environmental impact caused by the dispersion of medical waste. In this work, tomato peel recovered cutin was blended with poly(L-lactide-co-ε-caprolactone) (PLAPCL) to develop new textiles for medical application through electrospinning. The textile fabrication process was studied by varying Cut content in the starting suspensions and by optimizing fabrication parameters. Devices with dense and porous structures were developed, and their morphological, thermal, and physical–chemical properties were evaluated through scanning electron microscopy, differential scanning calorimetry, thermogravimetric analysis, and Fourier transformed infrared spectroscopy. Textile material stability to γ-irradiation was evaluated through gel permeation chromatography, while its wettability, mechanical properties, and biocompatibility were analyzed through contact angle measurement, tensile test, and MTT assay, respectively. The LCA methodology was used to evaluate the environmental impact of textile production, with a specific focus on greenhouse gas (GHG) emissions. The main results demonstrated the suitability of PLAPCL–cutin blends to be processed through electrospinning and the obtained textile’s suitability to be used to develop surgical face masks or patches for wound healing. Full article

Agricultural waste derivatives, particularly tomato cutin, a biopolymer found in the cuticular layer of plants, present a promising alternative for the development of sustainable materials in biomedical applications. Cutin, composed primarily of fatty acids and hydroxy acids, exhibits favorable biodegradability, biocompatibility, and hydrophobic properties, positioning it as a viable candidate for applications such as drug delivery systems, wound healing, and tissue engineering. This study investigates the extraction, characterization, and potential biomedical utilization of 10,16-dihydroxy hexadecenoic acid monomer derived from tomato cutin agro-waste. The cytotoxicity of cutin-based materials was evaluated through in vitro assays, demonstrating minimal toxicity and confirming their suitability for biomedical applications. The extraction process was optimized using various solvents, and the molecular characteristics of the extracted monomer were assessed using techniques such as Gel Permeation Chromatography (GPC), Gas Chromatography–Mass Spectroscopy (GC-MS) ¹H and ¹³C Nuclear Magnetic Resonance (NMR), Fourier Transformed Infrared (FT-IR) spectroscopy, Thermogravimetric Analysis (TGA), and Differential Scanning Calorimetry (DSC). MTT assay was also performed on NHDFs cultured in monomer solutions to assess their cytocompatibility. The findings suggest that cutin-based materials, when processed under environmentally sustainable conditions, offer an effective and biocompatible alternative to conventional synthetic polymers, opening new avenues for the development of sustainable biomedical products. Full article

Hydrogen is a promising alternative to fossil fuels, but its efficient storage presents significant challenges. Polymer composite vessels, especially those made from carbon fiber-reinforced plastic (CFRP), are gaining attention, due to their high strength-to-weight ratio for storing compressed or cryogenic hydrogen. The latest Type V tanks, which lack internal liners, rely solely on fiber composites for both structural integrity and gas containment, enhancing the storage volume-to-weight ratio and supporting recycling. However, this linerless design faces the challenge of preventing gas permeation. Epoxy resins, widely used in aerospace carbon fiber-reinforced composites (CFRCs), offer excellent processability and load-bearing capabilities. The addition of high-aspect-ratio nanofillers can enhance the gas barrier properties, which are essential for preventing hydrogen leakage, while also improving the mechanical, electrical, and thermal properties of the nanocomposites. This study focuses on epoxy-based composites with expanded graphite, aiming to optimize their physical properties and processing for Type V tanks, using a rheological framework to evaluate their processability and multifunctionality in transport applications. Full article

Nanoarchitectonics influences the properties of objects at micro- and even macro-scales, aiming to develop better structures for protection of product. Although its applications were analyzed in different areas, nanoarchitectonics of food packaging—the focus of this review—has not been discussed, to the best of our knowledge. The (A) structural and (B) functional hierarchy of food packaging is discussed here for the enhancement of protection, extending shelf-life, and preserving the nutritional quality of diverse products including meat, fish, dairy, fruits, vegetables, gelled items, and beverages. Interestingly, the structure and design of packaging for these diverse products often possess similar principles and methods including active packaging, gas permeation control, sensor incorporation, UV/pulsed light processing, and thermal/plasma treatment. Here, nanoarchitechtonics serves as the unifying component, enabling protection against oxidation, light, microbial contamination, temperature, and mechanical actions. Finally, materials are an essential consideration in food packaging, particularly beyond commonly used polyethylene (PE), polypropylene (PP), polyethylene terephthalate (PET), polystyrene (PS), and polyvinyl chloride (PVC) plastics, with emphasis on biodegradable (polybutylene succinate (PBS), polyvinyl alcohol (PVA), polycaprolactone (PCL), and polybutylene adipate co-terephthalate (PBAT)) as well as green even edible (bio)-materials: polysaccharides (starch, cellulose, pectin, gum, zein, alginate, agar, galactan, ulvan, galactomannan, laccase, chitin, chitosan, hyaluronic acid, etc.). Nanoarchitechnotics design of these materials eventually determines the level of food protection as well as the sustainability of the processes. Marketing, safety, sustainability, and ethics are also discussed in the context of industrial viability and consumer satisfaction. Full article

NaZSM-5 powder and membranes were hydrothermally prepared. Their (1) steam (H₂O) adsorption properties and (2) the permeation and separation of gas and H₂O were evaluated before and after the cation exchange of Na⁺ to K⁺ or Cs⁺. The quantity of adsorbed H₂O decreased as the size of the cation increased, indicating that the micropore volume and effective pore size of ZSM-5 decreased after cation exchange. The H₂ and N₂ permeances after cation exchange were less than 5% of the values before cation exchange, indicating a significant reduction in gas permeability. In contrast, the reduction of the H₂O permeance values of the ZSM-5 membranes before and after K⁺ or Cs⁺ exchange was lower than that of H₂, resulting in improved H₂O/H₂ separation performance. Compared with the NaZSM-5 membrane, the K⁺- or Cs⁺-exchanged ZSM-5 membranes exhibited superior H₂O permselectivity, particularly at dilute H₂O concentrations (<1 vol%). Full article

The hydrogen embrittlement of a typical Oil Country Tubular Good (OCTG) steel, API 5CT T95, was investigated through electrochemical hydrogen pre-charging followed by mechanical testing. J-integral and tensile tests were performed on electrochemically pre-charged samples, with varying charging conditions to simulate different hydrogen environmental exposure. Hydrogen concentration profiles during the electrochemical hydrogen charging process and subsequent mechanical testing in air were calculated with the support of hydrogen permeation tests and Finite Elements Method (FEM) mass diffusion analysis. This approach enabled a deeper understanding of the actual impact of hydrogen on the assessed mechanical properties. The results were compared with tests performed in air and with data available in the literature and were critically analyzed and discussed. A toughness reduction of up to 60% was observed under the most severe charging conditions; however, the alloy retained good ductility with a critical stress intensity factor of 124 MPa√m, well above the minimum values required for pipelines in high-pressure hydrogen gas and sour service applications, 55 MPa√m and 30 MPa√m, respectively, as specified by current ASME Standard and EFC Guidelines. Tensile tests on pre-charged specimens exhibited certain limitations due to the rapid hydrogen desorption rate with respect to the time required to conduct proper slow strain-rate tests. Full article

The primary extraction way for unconventional oil/gas resources is hydraulic fracturing to alter the reservoir for commercial production. However, hydraulic fracturing technology consumes a large amount of water, and the flowback water can easily be mixed with hydrocarbon substances to form emulsions. To achieve the recycling of water, it is necessary to develop an efficient continuous demulsification method for treating the flowback fluid. In this study, a composite filtration layer with superhydrophilic and superoleophilic properties was successfully prepared using water-based polyurethane as a binder. The g-C₃N₄ was used to improve the affinity of the filtration layer to water and oil. The diatomite and rice husk carbon were used as an adsorbent and a filter aid, respectively. The contact angles (CA) of both oil and water on the surface of the filtration layer were measured to be 0°. During the demulsification process, vacuum filtration was employed to increase the pressure difference across the filtration layer, thereby improving the treatment flux of flowback fluid. The experimental results showed that the filtration flux with the addition of rice husk charcoal increased from 160.58 L∙m⁻²∙h⁻¹ to 174.68 L∙m⁻²∙h⁻¹ compared to the filter layer without rice husk charcoal. Based on the composite filtration layer, the apparent demulsification efficiency exceeded 90.6% for various types of emulsion. The mechanism of demulsification was investigated by the molecular dynamics method. The results showed that the adsorption layer density of water molecules reached 1.5 g/cm³, and the adsorption layer density of oil molecules exceeded 2.5 g/cm³. The porous structure wall has a strong adsorption effect on both oil and water molecules, resulting in deformation and destruction of the oil–water interface, so that the dispersed phase is adsorbed and aggregated by the filter layer at the same time and permeates from the filter layer after reaching saturation, thus separating the two phases. Full article

This work addressed the fine dispersion of Multiwalled Carbon Nanotubes (MWCNTs) in a polymer matrix to obtain Mixed Matrix Membranes (MMMs) suited for gas separation. Not-purified MWCNTs were effectively loaded within a polyether block amide (Pebax^®2533) matrix, up to 24 wt%, using ultrasonication as well as a third component (polysorbate) in the dope solution. The obtained flexible thin films were investigated in terms of morphology, thermal properties, characterized by SEM, FT-IR, DSC, TGA, and gas permeation tests. The response to temperature variations of gas permeation through these nanocomposite specimens was also investigated in the temperature range of 25–55 °C. Defect-free samples were successfully obtained even at a significantly high loading of CNTs (up to 18 wt%), without a pre-treatment of the fillers. A remarkable enhancement of gas permeability upon the nanocarbons loading was reached, with a threshold value at a loading of ca. 7 wt%. The addition of polysorbates in the ternary MMMs further improves the dispersion of the filler, enhancing also the permselectivity of the membrane. Full article

The large-scale implementation of 2D material-based membranes is hindered by mechanical stability and mass transport control challenges. This work describes the fabrication, characterisation, and testing of self-standing graphene oxide (GO) membranes cross-linked with oxides such as Fe₂O₃, Al₂O₃, CaSO₄, Nb₂O₅, and a carbide, SiC. These cross-linking agents enhance the mechanical stability of the membranes and modulate their mass transport properties. The membranes were prepared by casting aqueous suspensions of GO and SiC or oxide powders onto substrates, followed by drying and detachment to yield self-standing films. This method enabled precise control over membrane thickness and the formation of laminated microstructures with interlayer spacings ranging from 0.8 to 1.2 nm. The resulting self-standing membranes, with areas between 0.002 m² and 0.090 m² and thicknesses from 0.6 μm to 20 μm, exhibit excellent flexibility and retain their chemical and physical integrity during prolonged testing in direct contact with ethanol/water and methanol/water mixtures in both liquid and vapour phases, with stability demonstrated over 24 h and up to three months. Gas permeation and chemical characterisation tests evidence their suitability for gas separation applications. The interactions promoted by the oxides and carbide with the functional groups of GO confer great stability and unique mass transport properties—the Nb₂O₅ cross-linked membranes present distinct performance characteristics—creating the potential for scalable advancements in cross-linked 2D material membranes for separation technologies. Full article