CO2 Gas Permeability Research Articles

Exploring the feasibility of biodegradable films for antimicrobial absorbent sachets and CO2 emitters as sustainable active packaging

The use of biodegradable polymer films for packaging materials as eco-friendly alternatives to traditional plastics is limited by their water sensitivity and poor gas barrier properties. This study developed a multifunctional supplemental packaging system using poly(butylene adipate-co-terephthalate) (PBAT) and thermoplastic starch (TPS) blend film incorporated with 3% and 5% zinc oxide (ZnO) nanoparticles. The system targets the triple-active packaging displayed antimicrobial activity with water absorption and CO2 emission properties. ZnO incorporation effectively reduced water solubility of the PBAT/TPS film (from 16% to 7%), and exhibited excellent antimicrobial activity against Gram-positive and Gram-negative bacteria (>99% reduction). Well-dispersed ZnO, verified by scanning electron microscopy, decreased water vapor and CO2 gas permeation. A PBAT/TPS-ZnO sachet was fabricated, comprising carboxymethyl cellulose as the absorbent function and CO2 precursors (sodium bicarbonate and citric acid). The 3% ZnO loading achieved optimal performance, balancing water absorption (2.48 g weight gain after 144 h) and CO2 emission (35% in headspace at equilibrium). Kinetic studies suggested diffusion as the dominant mechanism for CO2 release, driven by concentration differences between the sachet and headspace. This system showed potential as active modified atmosphere packaging to extend product shelf life.

Investigating temperature-dependent gas permeation in PIM-1: Hysteresis, annealing effects, and thermal history impact

This study investigates the gas permeability, diffusion coefficients, and solubility coefficients of CO2 and N2 in PIM-1 over the temperature range of 35 °C–135 °C. During the first heating-cooling cycle, both gases' permeability exhibited hysteresis, which diminished during the second cycle. Thermal mechanical analysis confirmed volume relaxation occurring at temperatures above 95 °C, indicating physical aging. By calculating the relaxation time associated with volume relaxation, the influence of physical aging was minimized through measurements on samples annealed at 135 °C for 15 h. This approach enabled a successful evaluation of the temperature dependence of gas permeability under conditions where the impact of physical aging could be disregarded. The results revealed that the permeability of CO2 decreased, and that of N2 increased with increasing temperature. The diffusion coefficients showed positive temperature dependence, while the solubility coefficients decreased. Physical aging significantly affected the diffusion coefficients but had minimal impact on the solubility coefficients. Heat of sorption and activation energies for gas permeability and diffusion estimated, and it was found that the decrease in CO2 permeability with temperature was mainly attributed to the large heat of sorption for CO2.

Unique Self-Phosphorylating Polybenzimidazole of the 6F Family for HT-PEM Fuel Cell Application.

High-temperature polymer-electrolyte membrane fuel cells (HT-PEMFCs) are a very important type of fuel cells since they operate at 150-200 °C, making it possible to use hydrogen contaminated with CO. However, the need to improve the stability and other properties of gas-diffusion electrodes still impedes their distribution. Self-supporting anodes based on carbon nanofibers (CNF) are prepared using the electrospinning method from a polyacrylonitrile solution containing zirconium salt, followed by pyrolysis. After the deposition of Pt nanoparticles on the CNF surface, the composite anodes are obtained. A new self-phosphorylating polybenzimidazole of the 6F family is applied to the Pt/CNF surface to improve the triple-phase boundary, gas transport, and proton conductivity of the anode. This polymer coating ensures a continuous interface between the anode and proton-conducting membrane. The polymer is investigated using CO2 adsorption, TGA, DTA, FTIR, GPC, and gas permeability measurements. The anodes are studied using SEM, HAADF STEM, and CV. The operation of the membrane-electrode assembly in the H2/air HT-PEMFC shows that the application of the new PBI of the 6F family with good gas permeability as a coating for the CNF anodes results in an enhancement of HT-PEMFC performance, reaching 500 mW/cm2 at 1.3 A/cm2 (at 180 °C), compared with the previously studied PBI-O-PhT-P polymer.

Coconut husk-lignin derived carbon dots incorporated carrageenan based functional film for intelligent food packaging

Carbon dots (CDs) derived from sustainable natural feed-stocks like lignin have gained wide acceptance by virtue of their renewability and promising potential in intelligent sensing applications. The precursor lignin is isolated from agro-biomass waste, coconut husk through sodium hydroxide based extraction process. CDs are synthesised from amine functionalized lignin through solvothermal process and integrated into carrageenan biopolymer matrix (1, 2 and 3 wt%). The composite film with 2 wt% CDs (CARR2CD) showed optimum fluorescent emission intensity, excellent pH dependent fluorescent color change in the food pH range, reasonable tensile strength (46.50 ± 1.32 MPa) and 27 % increase in elongation at break. CDs imparted UV-light blocking properties (70 % UV-light) and enhanced hydrophobicity of the carrageenan matrix. CARR2CD film showed 84 % visible light transparency, 79 % reduction in oxygen transmittance rate (OTR), 81 % reduction in CO2 gas permeability and excellent antioxidant and antibacterial properties (against E. coli and S. aureus). As a practical application, the developed responsive packaging material is used to track pH change associated with milk spoilage via noticeable color change in fluorescent emission of the composite film. Thus, the developed responsive composite film paves a way for use as green and sustainable transparent intelligent food packaging material.

Design of equilibrium modified atmosphere packaging for postharvest cabbages preservation based on introducing available active sites into film materials as gas transport channels

This work aims to explore an available avenue to design an equilibrium modified atmosphere packaging (EMAP) by the modification of gas permeability of material. In this work, the introduction of available active sites endowed materials with adjustable gas permeability properties. With varying concentrations of the resulting materials with various gas permeability, the CO2 and O2 gas permeability of the blending films were modified at the range of 3.92 ∼ 17.84 barrier and 0.65 ∼ 3.46 barrier, respectively. On this basis, the films were used as EMAP to preserve postharvest cabbages. The results indicated that each EMAP achieved an equilibrium atmosphere containing 6.8 % ∼ 3.8 % CO2 and 2.1 % ∼ 5.2 % O2 within 15 h and maintained it continuously. In these atmosphere, the respiratory rate of the preserved cabbages was significantly inhibited, thereby delaying the deterioration of their storage quality. As the results, sensory scores of the preserved samples were maximally maintained. Declines of color indexes and texture indexes were obviously inhibited. Chemical variations in chlorophyll content, total phenolics content, total flavonoids content, ascorbic acid and nitrite content were significantly suppressed. The overall findings revealed that this method is suitable and promising to develop EMAP for the postharvest vegetables.

A unique anti-corrosion composite coating with CO2 gas barrier and acid resistance suitable for CCUS environment

In the process of carbon capture, utilization and storage (CCUS), carbon dioxide is in long-term contact with metal pipelines and devices. Therefore, in the CCUS environment the corrosion of carbon dioxide to metals limits the service life. Herein we have explored the failure of epoxy (EP) coating in the CO2 corrosion environment. Based on this, a unique g-C3N4-ESO-EP anti-corrosion coating suitable for CCUS conditions was prepared by using graphene-C3N4 (g-C3N4) nanosheet and epoxy silane oligomer (ESO) one-step method. The semiconductor g-C3N4 prepared by the secondary thermal stripping method provides plentiful CO2 adsorption sites and prevents the diffusion of corrosive ions (gathered state CO2, CO32−, HCO3−, H+) in the EP coating. The CO2 gas permeability of g-C3N4-ESO-EP film (with thickness of 100 μm) is approximately 45.94% lower than that of EP film. After immersion in 1.0 M acid corrosion environment, the protection efficiency of g-C3N4-ESO-EP coating is 99.99%. After adding ESO, the “bridging effect” formed at the interface reduces the interface defects between the resin and the nano-sheet, and synergistically enhances the adhesion between the coating and the substrate. The g-C3N4-ESO-EP coating has passed the test of severe simulated CCUS corrosion environment (4 days in 3.0 MPa CO2 and 3.5 wt% NaCl solution). The |Z|0.01Hz value of g-C3N4-ESO-EP coating after immersion in 3.5 wt% NaCl solution for 120 days maintained 1.73 × 1011 O cm2, indicating the coating has long-term corrosion resistance. This work provides a new and simple method to improve the CO2 resistance of EP coating and reveals the importance of functional composite coating for metal protection in CCUS process.

Gas permeation, thermal, morphology and mechanical properties of polyimide/clay nanocomposites: Effect of organically modified montmorillonite

Novel polyimide/clay nanocomposites were fabricated by incorporating organically modified clay at different loading percentage of 1–5 wt% within the polyimide (PI) matrix. A novel PI was synthesized through a direct polycondensation reaction between novel 5,5′-((4-methoxyphenyl)azanediyl)bis(isobenzofuran-1,3-dione)and 4,4′-(1,4-phenylenebis(oxy))bis(3-(trifluoromethyl)aniline). The organoclay was prepared from Sodium montmorillonite (Na-clay) and protonated form of diamine (modifier) via ion-exchange reaction. The structural characterization of nanocomposites were made using Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM), the mechanical properties were obtained by tension tests. The results of XRD, TEM, and FE-SEM indicated that clay could well disperse in the PI matrix and were intercalated by diamine and PI macromolecules. The thermal stability and glass transition temperature of nanocomposite at lower clay loadings are similar to PI but gradually decrease with increase in clay content. The tensile properties of PI/Clay nanocomposites showed the highest values at the optimum clay content of 3 wt%. The gas permeation of PI/clay nanocomposites was increased with the increase in loading percentage of organoclay, whereas the gas selectivity was maintained at par to that of neat PI film until it diminished at 5 wt% percentage of organoclay causing mineral agglomeration. PI/clay 3 wt% MMMs exhibited 245% and 240% increase in CO2 and O2 gas permeability respectively, while showing minimal variation in the selectivity of O2/N2 and CO2/N2 compared to that of neat PI matrix.

Design and optimization of multilayer composite membrane for biomethane enrichment: Process simulations and economics

The depletion of fossil fuels has led to the development of various biogas upgrading techniques that can be a reliable and sustainable energy source. At present, membrane-based gas separation and enrichment have received more acceptance to contend with the traditional biogas upgrading processes. Remarkably, multilayered composite membranes (MCM) fabricated from selective polymers and fillers have achieved high consideration in the field of CO2separation. In this regard, the present study focuses on fabricating and optimizing the porous layer of MCM using Polyether sulfone (PES) and Torlon polymers and their morphological influences on overall membrane performance. The MCM membranes fabricated from the PES porous substrate exhibited 3–4 fold higher permeation than the Torlon. Besides, the effect of zeolite type and % loading on the selective layer performance in CO2gas permeation was examined. From the gas permeation experiments, a 6 % loaded 3A zeolite sample exhibited maximum permeation flux for CO2, which is 1.7 folds compared to the neat Polyether block amide (PEBAX)/PES membrane and 5.8 fold to the neat PEBAX/Torlon without compromising the selectivity. Furthermore, process simulation using Aspen Hysys reveals the economic feasibility of membrane-based biomethane enrichment. Overall, the study results are compared with Robeson’s plot, which reveal the substantial potential of MCM-based membrane technology as a biogas upgrading process and offers assistance in developing an appropriate porous support for MCM.

Reinforcement of single-walled carbon nanotubes on polydimethylsiloxane membranes for CO2, O2, and N2 permeability/selectivity

In this study, PDMS incorporated with SWCNTs have been fabricated via solution casting method for industrial applications and characterized by the analyses of SEM, FTIR, TGA, AFM, and MST. The modified membranes were further analyzed for CO2, O2, and N2 gas permeability. The strategic membranes have five different weight ratios (0.013, 0.025, 0.038, 0.050, 0.063) compared to neat PDMS membranes. The even distribution of SWCNTs in PDMS provided results that showed improvement in thermal stability. However, mechanical strength has been weakened with increased concentration of nanofiller because of the increase in the number of SWCNTs by increases that imperfections become more severe. The designed polymeric membranes with good thermal stability and adequate mechanical strength can be used for the selectivity and permeability of CO2, O2, and N2 gases. The effect of the PDMS-SWCNTs on gas permeability has been studied. 0.063 wt.% SWCNTs presented the maximum permeability of CO2 gas while maximum O2 and N2 gas permeability have been obtained by 0.013 wt.% SWCNTs. The ideal selectivity of mixed (50:50) gas conditions has been tested. The maximum CO2/N2 ideal selectivity was obtained by 0.050 and 0.063 wt.% SWCNTs while maximum O2/N2 ideal selectivity obtained by 0.050 wt.% SWCNTs. Therefore, the fabrication of this novel SWCNTs-PDMS membrane may lead to separating the industrial exhaust and be used as a potential membrane for environmental remediation in the future.

Tailoring the Micropore Structure of 6FDA-Based Network Polyimide Membranes for Advanced Gas Separation by Decarboxylation

The 6FDA-based network PI has attracted significant attention for gas separation. A facile strategy to tailor the micropore structure within the network PI membrane prepared by the in situ crosslinking method is extremely significant for achieving an advanced gas separation performance. In this work, the 4,4'-diamino-2,2'-biphenyldicarboxylic acid (DCB) or 3,5-diaminobenzoic acid (DABA) comonomer was incorporated into the 6FDA-TAPA network polyimide (PI) precursor via copolymerization. The molar content and the type of carboxylic-functionalized diamine were varied in order to easily tune the resulting network PI precursor structure. Then, these network PIs containing carboxyl groups underwent further decarboxylation crosslinking during the following heat treatment. Properties involving thermal stabilities, solubility, d-spacing, microporosity, and mechanical properties were investigated. Due to the decarboxylation crosslinking, the d-spacing and the BET surface areas of the thermally treated membranes were increased. Moreover, the content of DCB (or DABA) played a key role in determining the overall gas separation performance of the thermally treated membranes. For instance, after the heating treatment at 450 °C, 6FDA-DCB:TAPA (3:2) showed a large increment of about ~532% for CO2 gas permeability (~266.6 Barrer) coupled with a decent CO2/N2 selectivity~23.6. This study demonstrates that incorporating the carboxyl-containing functional unit into the PI backbone to induce decarboxylation offers a practical approach with which to tailor the micropore structure and corresponding gas transport properties of 6FDA-based network PIs prepared by the in situ crosslinking method.

Polydimethylsiloxane/Magnesium Oxide Nanosheet Mixed Matrix Membrane for CO2 Separation Application

Carbon dioxide (CO2) concentration is now 50% higher than in the preindustrial period and efforts to reduce CO2 emission through carbon capture and utilization (CCU) are blooming. Membranes are one of the attractive alternatives for such application. In this study, a rubbery polymer polydimethylsiloxane (PDMS) membrane is incorporated with magnesium oxide (MgO) with a hierarchically two-dimensional (2D) nanosheet shape for CO2 separation. The average thickness of the synthesized MgO nanosheet in this study is 35.3 ± 1.5 nm. Based on the pure gas separation performance, the optimal loading obtained is at 1 wt.% where there is no observable significant agglomeration. CO2 permeability was reduced from 2382 Barrer to 1929 Barrer while CO2/N2 selectivity increased from only 11.4 to 12.7, and CO2/CH4 remained relatively constant when the MMM was operated at 2 bar and 25 °C. Sedimentation of the filler was observed when the loading was further increased to 5 wt.%, forming interfacial defects on the bottom side of the membrane and causing increased CO2 gas permeability from 1929 Barrer to 2104 Barrer as compared to filler loading at 1 wt.%, whereas the CO2/N2 ideal selectivity increased from 12.1 to 15.0. Additionally, this study shows that there was no significant impact of pressure on separation performance. There was a linear decline of CO2 permeability with increasing upstream pressure while there were no changes to the CO2/N2 and CO2/CH4 selectivity.

Design, synthesis and characterization of novel fluorinated polyimide membranes with bulky pendant for gas transport

AbstractThree novel fluorinated polyimides (PIs) were synthesized via one‐step solution polycondensation from a new diamine monomer, 4‐(3‐methoxy‐4‐(difluoromethoxy)phenyl)‐2,6‐bis(4‐aminophenyl)pyridine, and three commercially available aromatic dianhydrides. The solubility, thermal, optical, hydrophobic and gas transport properties of the obtained PIs were investigated. The results demonstrated that these polymers present good solubility in dimethylformamide, N‐methylpyrrolidone, dimethylsulfoxide, dimethylacrylamide, CHCl3, tetrahydrofuran and CH2Cl2 at room temperature or upon heating. Meanwhile, they displayed excellent thermal properties with glass transition temperature of 261–345 °C, weight loss temperatures at 10% of 518–523 °C as well as char yield of 60–62% at 800 °C in nitrogen atmosphere. Furthermore, the PI membranes have good hydrophobic properties with water contact angle value in the range 90.1–92.0°. Moreover, they show excellent optical properties, with cut‐off wavelength (λcut‐off) values of 368–381 nm and wavelength values at 80% transmittance (λ80%) of 421–462 nm. The pure gas permeabilities of He, CO2, O2 and N2 of the PI membranes were measured by the method of constant volume–variable pressure. The PI containing 4,4′‐(hexafluoroisopropyl)diphthalic anhydride moiety exhibits the largest molecular chain spacing and free volume, giving the best gas transport performance in this work. Molecular simulation results show that the introduction of fluorine‐containing structure and bulky pendant into polymer backbones is beneficial for gas transport. © 2023 Society of Industrial Chemistry.

Attapulgite Nanorod-Incorporated Polyimide Membrane for Enhanced Gas Separation Performance.

Polyimide (PI) membrane is an ideal gas separation material due to its advantages of high designability, good mechanical properties and easy processing; however, it has equilibrium limitations in gas selectivity and permeability. Introducing nanoparticles into polymers is an effective method to improve the gas separation performance. In this work, nano-attapulgite (ATP) functionalized with KH-550 silane coupling agent was used to prepare polyimide/ATP composite membranes by in-situ polymerization. A series of characterization and performance tests were carried out on the membranes. The obtained results suggested a significant increase in gas permeability upon increasing the ATP content. When the content of ATP was 50%, the gas permeability of H2, He, N2, O2, CH4, and CO2 reached 11.82, 12.44, 0.13, 0.84, 0.10, and 4.64 barrer, which were 126.87%, 119.40%, 160.00%, 140.00%, 150.00% and 152.17% higher than that of pure polyimide, respectively. No significant change in gas selectivity was observed. The gas permeabilities of membranes at different pressures were also investigated. The inefficient polymer chain stacking and the additional void volume at the interface between the polymer and TiO2 clusters leaded to the increase of the free volume, thus improving the permeability of the polyimide membrane. As a promising separation material, the PI/ATP composite membrane can be widely used in gas separation industry.

Machine learning enables interpretable discovery of innovative polymers for gas separation membranes.

Polymer membranes perform innumerable separations with far-reaching environmental implications. Despite decades of research, design of new membrane materials remains a largely Edisonian process. To address this shortcoming, we demonstrate a generalizable, accurate machine learning (ML) implementation for the discovery of innovative polymers with ideal performance. Specifically, multitask ML models are trained on experimental data to link polymer chemistry to gas permeabilities of He, H2, O2, N2, CO2, and CH4. We interpret the ML models and extract valuable insights into the contributions of different chemical moieties to permeability and selectivity. We then screen over 9 million hypothetical polymers and identify thousands that lie well above current performance upper bounds, including hundreds of never-before-seen ultrapermeable polymer membranes with O2 and CO2 permeability greater than 104 and 105 Barrers, respectively. High-fidelity molecular dynamics simulations confirm the ML-predicted gas permeabilities of the promising candidates, which suggests that many can be translated to reality.

Environmental treatment and remediation using h-BN based smart and hybrid membrane

Corrosion is a major problem resulting from acid gases found in natural gas being transported in pipelines. To solve this problem, high aspect ratio h-BN nanosheets have been incorporated and are properly assimilated in the CA matrix, this led to an increase in tortuous path of flow for the gas resulting in smooth, dense membrane samples causing exceptional permeability reduction. Hexagonal Boron Nitride (h-BN) nanosheets have been synthesized and incorporated into cellulose acetate (CA) matrix using solution casting method. Nanosheets of various sizes, separated by varying centrifugation speeds (i.e. 500 rpm, 700 rpm, 1500 rpm, 2000 rpm and 2500 rpm), have been prepared and used for our work. The resulting nanocomposites, having thickness ranging between 40 and 60 μm, were then tested for CO2 gas permeability reduction using both short-term (8 h) tests as well as long-term (72-h tests). As a result of these tests, a maximum CO2 permeability reduction of 99.84% is found with a minimum CO2 permeability of 3.25 barrer. For dimensional analysis of both nanosheets and nanocomposites, scanning electron microscopy (SEM) analysis is used. For verifying the presence of the required functional groups in our synthesized samples, FT-IR spectroscopy is used. Moreover, to confirm the presence of crystalline phases, X-ray Diffraction (XRD) analysis is used. Also, tensile testing is used to analyze the mechanical robustness and it was found that nanocomposite samples exhibited higher tensile strength as compared to pristine samples. Furthermore, tribological property analysis was also carried out for adhesion testing of polymeric material with steel.

Gamma Irradiation of Cellulose Acetate-Polyethylene Glycol 400 Composite Membrane and Its Performance Test for Gas Separation

Gas separation processes through membrane permeation have attracted the attention of researchers recently due to their promising applications. In this study, we modified the cellulose acetate (CA) membrane to improve the membrane performance of CO2/CH4 gas separation. The CA membrane was modified by adding polyethylene glycol (PEG) 400 as the carrier and N, N’-methylenebisacrylamide (MBA) as the cross-linking agent. Gamma-ray from cobalt 60 was used as a reaction initiator with variation in irradiation doses. The membrane characterization tests were conducted using scanning electron micrograph (SEM), Fourier transforms infrared (FTIR), and instron tensile strength tester. The permeability and selectivity of the membranes were tested against the single gases CO2 and CH4. The SEM analysis showed the morphology change in the membrane surface by gamma irradiation and a crosslinking agent. The spectra of FTIR showed a change in peak intensity on several polymer functional groups in the presence of gamma-ray irradiation. The tensile strength test showed that membranes with MBA have a higher mechanical strength than those without MBA. Based on the membrane permeability and selectivity tests, CO2 gas permeability was affected by pressure. The ideal selectivity of CO2/CH4 shows that the irradiated membrane has a higher selectivity than that of the non-irradiated membrane.

Can Edible Coatings Maintain Sweet Pepper Quality after Prolonged Storage at Sub-Optimal Temperatures?

This work evaluated the efficacies of different coatings: chitosan, gelatin and chitosan-gelatin applied layer-by-layer (LbL); for maintaining the quality of sweet peppers that were stored for 3 weeks at a sub-optimal temperature (1.5 °C) and at an optimal storage temperature (7 °C). After the cold-storage period, fruits were kept under marketing conditions (21 °C) for 3 more days. An edible chitosan coating (2%) effectively alleviated chilling injury and the incidence of decay, and also preserved the nutritional quality of sweet peppers that were kept for 3 weeks at 1.5 °C plus 3 more days at 21 °C. The chitosan coating was more effective than the two other coatings. All three coating treatments significantly reduced external CO2 production, as compared to uncoated control fruit. Storage temperatures did not significantly affect external CO2 production, although CO2 production was slightly higher at 1.5 °C. The chitosan coating exhibited good CO2 gas permeability properties and the peppers coated with that material had lower respiration rates than those in the other two experimental treatments or the control. From a practical point of view, chitosan coating could replace the plastic bags previously found to alleviate chilling injury in peppers that are stored at 1.5 °C as a quarantine treatment.

Effect of graphene nanoplatelets on the mechanical and gas barrier properties of woven carbon fibre/epoxy composites

Carbon-fibre-reinforced polymer (CFRP) composites are promising materials for non-metallic pipe applications in the oil and gas industry owing to their high corrosion resistance, specific strength and stiffness. However, CFRP has poor gas barrier performance meaning that a liner has to be inserted. Graphene-based nanomaterials have been demonstrated to improve gas barrier properties in thermoplastic polymers, and thus, a CFRP–graphene hybrid composite could provide an alternative to lined pipes. In this work, a method combining spray coating with vacuum-assisted resin infusion was developed to fabricate CFRP hybrid composites with preferred in-plane aligned graphene nanoplatelets. Tensile and flexural properties, as well as CO2 gas permeability, were evaluated. It was illustrated that both tensile and flexural properties performed better under relatively low GNP loadings (< 0.2 vol%), while gas barrier property was significantly improved with the increasing GNP loadings which fits the Nielsen model with an effective GNP aspect ratio of 350.Graphical abstract

Structure-Property Relationship of Cellulose Nanocrystal-Polyvinyl Alcohol Thin Films for High Barrier Coating Applications.

CO2 and O2 gas permeability are paramount concerns in food packaging. Here, the permeability of cellulose nanocrystals (CNCs) and polyvinyl alcohol (PVA) coatings was explored as it relates to varied CNC content. Specifically, this work focuses on the role of PVA in rheology and barrier performance of the CNC films. Results show that shear-casted CNC films are transparent and have a high-order parameter, which is attributed to the shear-thinning behavior of the CNCs. The barrier performance of the CNC films improved because of the synergistic effect of having both alignment of CNCs and a lower free volume. The CNC-PVA films exhibited excellent barrier performance as compared to traditional engineered polymers, even much higher than high barrier ethylene-vinyl alcohol copolymer films. Furthermore, the moisture sensitivity of the films was greatly diminished with the addition of PVA. Overall, the results show applicability of CNC-PVA coating formulations for high barrier packaging applications.

Effect of silica nanoparticles on carbon dioxide separation performances of PVA/PEG cross-linked membranes

Novel PVA/PEG cross-linked membranes were prepared with (0–20 wt. %) of silica nanoparticles. The presence of both the polymers and additive was confirmed by FTIR analysis. The thermal properties of the membranes were analyzed by TGA and DSC analysis. The morphological and mechanical properties of the membranes were studied by SEM analysis and tensile testing, respectively. The gas permeation performances of the membranes were examined using state-of-the-art gas permeability cell. It was found that permeability of all the gases increased with the increase of silica loading, whereas ideal selectivity of carbon dioxide with respect to nitrogen and methane increased up to 10 wt. % loading and then became nearly constant on further loading. 20 wt. % silica loaded membrane was found to be the best performance membrane. The gas permeability of CO2 was also compared with different gas permeation models and was found to be in close agreement with Maxwell Model. The effect of temperature and pressure of feed gas pressure was also studied on permeation performances and optimum performances were achieved around 65 °C. The gas permeation performances were observed to decrease slightly with the increase in feed gas pressure up to 20 bar which confirms the absence of plasticization phenomenon up to 20 bar. Finally, gas permeation performances were compared with 2008 Robeson trade-off lines and it was found that at 20 wt. % loading, gas permeation performances surpassed the trade-off line for CO2/N2, and for CO2/CH4, the gas permeation performances approached the trade-off line.