Temperature dependency of gas barrier properties of biodegradable PP/PLA/nanoclay films: Experimental analyses with a molecular dynamics simulation approach

Polypropylene (PP)/poly(lactic acid) (PLA)/clay nanocomposite films with various compositions (PP‐rich and PLA‐rich) were prepared. Their structural and barrier properties against CO₂, O₂, and N₂ were investigated. The microstructure of the nanocomposites was studied by scanning electron microscopy, transmission electron microscopy, and wide angle X‐ray scattering. The PP‐rich with 75/25 composition revealed the best barrier properties against all the gases which could be justified according to its microstructure. Selectivity of O₂/N₂ and CO₂/N₂ was also measured. It was found that the addition of nanoclay as a gas barrier component reduced the permeability in both systems. The permselectivity was also reduced in the PP‐rich films while it was increased in the PLA‐rich system. Moreover, the temperature dependency of permeability, selectivity, and permselectivity for PP, PLA, and PP/PLA (75/25) samples was examined. The results showed that the temperature dependence of permeability obeyed an Arrhenius equation and order of activation energy of permeability for O₂, CO₂, and N₂ gases was found to be E_P < E_P/PLA < E_PLA. According to solubility measurements, the order of solubility coefficient for gases was as follows: CO₂ > O₂ > N₂. Finally, the molecular dynamics (MD) simulation was performed to estimate the diffusivity coefficients of the gases and showed that solubility increases with increasing temperature, which was in accordance with the experiments. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46665.     

House of Cards Nanostructuring of Graphene Oxide and Montmorillonite Clay for Oil–Water Separation

Noncovalent interactions are ubiquitous in our daily living. Nature employs hydrophobic effects, π–π interactions, hydrogen bonding, van der Waals forces, and electrostatic interactions in many biological processes such as protein folding. In the same manner, scientists exploit this plethora of inherently reversible noncovalent interactions as dials to design robust and smart materials. Electrostatic interaction is particularly interesting due to the simplicity of its concept, i.e., opposite charges attract. However, to our knowledge, the electrostatic interaction between two different 2D nanomaterials has not been investigated in literature. A myriad of natural and synthetic 2D nanomaterials should be explored for what may be an exciting cocktail of synergistic and tunable properties brought about by their charges and physical properties. This contribution highlights an interesting phenomena when organic, negatively charged graphene oxide and inorganic, positively charged montmorillonite (MMT) clay edges are brought into contact.     

Laser transmission welding of poly(lactic acid) and polyamide66/sepiolite nanocomposites

Influence of sepiolite nanoclay on the properties of the resulting join between poly(lactic acid) (PLA) and different Polyamide66 (PA66)/nanoclay nanocomposites was studied in this work. Six different polymer nanocomposites based on PA66 were manufactured through a melt compounding process by adding a fixed 1.64 wt % of a commercial IR absorber additive and the respective weight percentages of sepiolite to the polymer matrix. Several nanocomposite/PLA joints were finally performed by means of the transmission laser welding technology and the resulting weldings were characterized in terms of mechanical properties by performing peeling and shearing tests. Furthermore, both welded and mechanically tested samples were also analyzed by scanning electron microscopy in order to study the morphology of the weld seam. The results of the performed tests show that the addition of sepiolite to the PA66 improves the welding performance only in those cases in which the percentage of sepiolite of the nanocomposites is higher than 5 wt %. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46638.     

Influence of nanoclay on urea–glyoxalated lignin–formaldehyde resins for wood adhesive

In this research, the influence of nanoclay on urea–glyoxalated lignin–formaldehyde (GLUF) resin properties has been investigated. To prepare the GLUF resin, glyoxalated soda baggase lignin (15 wt%) was added as an alternative for the second urea during the UF resin synthesis. The prepared GLUF resin was mixed with the 0.5%, 1%, and 1.5% nanoclay by mechanically stirring for 5 min at room temperature. The physicochemical properties of the prepared resins were measured according to standard methods. Then the resins were used in particleboard production and the physical and mechanical properties of the manufactured panels were determined. Finally, from the results obtained, the best prepared resin was selected and its properties were analyzed by differential scanning calorimetry (DSC), Fourier transform infrared spectrometry (FTIR), and X-ray diffractometry (XRD). Generally the results indicated that the addition of sodium-montmorillonite (NaMMT) up to 1.5% appears to improve the performance of GLUF resins in particleboards. The results also showed that nanoclays improved mechanical strength (modulus of elasticity (MOE), Modulus of Rupture (MOR), and internal bond (IB) strength) of the panels bonded with GLUF resins. The panels containing GLUF resin and nanoclay yielded lower formaldehyde emission as well as water absorption content than those made from the neat GLUF resins. XRD characterization indicated that NaMMT only intercalated when mixed with GLUF resin. Based on DSC results, the addition of NaMMT could accelerate the curing of GLUF resins. The enthalpy of the cure reaction (ΔH) of GLUF resin containing NaMMT was increased compared with neat GLUF resin. Also the results of FTIR analysis indicated that addition of NaMMT change the GLUF resins structures.     

Injectable polyethylene glycol-laponite composite hydrogels as articular cartilage scaffolds with superior mechanical and rheological properties

In this study, injectable PEG-based hydrogels containing Laponite particles with mechanical and structural properties close to the natural articular cartilage are introduced. The nanocomposites are fabricated by imide ring opening reactions utilizing synthesized copolymers containing PEG blocks and nanoclay through a two-step thermal poly-(amic acid) process. Butane diamine is used as nucleophilic reagent and hydrogels with interconnected pores with sizes in the range of 100–250?µm are prepared. Improved viscoelastic properties compared with the conventional PEG hydrogels are shown. Evaluation of cell viability utilizing human mesenchymal stem cells determines cytocompatibility of the nanocomposite hydrogels.     

Thermal Resistance and Application of Nanoclay on Polymer Flooding in Heavy Oil Recovery

High molecular weight and water-soluble synthetic organic polymers are currently being used in the field with the hope of enhancing the recovery of oil by water flooding. Nanotechnology has been used in many applications and new possibilities are discovered constantly. Recently, a renewed interest arises in the application of nanotechnology for the upstream petroleum industry. The author focuses on roles of clay nanoparticles on polymer viscosity. Polymer-flooding schemes for recovering residual oil have been in general less than satisfactory due to loss of chemical components by adsorption on reservoir rocks, precipitation, and resultant changes in rheological properties. Rheological properties changes are mainly determined by the chemical structure and mix of the polymers, surface properties of the rock, composition of the oil and reservoir fluids, nature of the added polymers, and solution conditions such as salinity and temperature. On the other hand, the author's focus is on viscosity, temperature, and salinity of solutions polyacrylamide polymer solutions with different nanoparticles. Results show that ultimate oil recovery by nanoclay polymer flooding enhances by a factor of 5.8% in comparison to polymer flooding high salinity and temperature.     

The Optimal Concentration of Nanoclay Hydrotalcite for Recovery of Reactive and Direct Textile Colorants

Concerns about the health of the planet have grown dramatically, and the dyeing sector of the textile industry is one of the most polluting of all industries. Nanoclays can clean dyeing wastewater using their adsorption capacities. In this study, as a new finding, it was possible to analyze and quantify the amount of metal ions substituted by anionic dyes when adsorbed, and to determine the optimal amount of nanoclay to be used to adsorb all the dye. The tests demonstrated the specific amount of nanoclay that must be used and how to optimize the subsequent processes of separation and processing of the nanoclay. Hydrotalcite was used as the adsorbent material. Direct dyes were used in this research. X-ray diffraction (XRD) patterns allowed the shape recovery of the hydrotalcite to be checked and confirmed the adsorption of the dyes. An FTIR analysis was used to check the presence of characteristic groups of the dyes in the resulting hybrids. The thermogravimetric (TGA) tests corroborated the dye adsorption and the thermal fastness improvement. Total solar reflectance (TSR) showed increased radiation protection for UV-VIS-NIR. Through the work carried out, it has been possible to establish the maximum adsorption point of hydrotalcite.     

Development of epoxy-cyanate ester-clay nanocomposites offering enhanced thermally stability

The preparation and characterization of blends of a series of dicyanate monomers such as 2,2′-bis(4-cyanatophenyl) propane (DCDPP), bis-4-cyanato-biphenyl (DCBP), bis-4-cyanatonaphthalene (DCN), 3,3′-bis(4-cyanatophenyl)sulphide (DCTDP), 3,3′-bis(4-cyanatophenyl)sulphone (DCDPS), and the diglycidyl ether of bisphenol A are reported. These copolymers are combined with a montmorillionite nanoclay and both epoxy-cyanate blends and epoxy-cyanate blends-nanoclay composites are all analyzed for thermal stability, thermal degradation kinetics, flame retardancy, and impact strength. The nanocomposites are further characterized by X-ray diffraction and SEM to determine morphological features, from which structure–property relationships are determined. Dispersion of the nanoclay is of paramount importance, but its inclusion serves to improve char yield and impact strength, when this is achieved. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47754.     

Structure and properties of nylon-6/amino acid modified nanoclay composite fibers

Biodegradable amino acid modified nanocaly was applied to produce nylon-6/nanoclay composite fibers using melt blending and melt spinning processes. Field emission scanning electron microscopy images showed that the surface of composite fibers was uniform and free from defects. Layer spacing of modified nanoclay was increased due to the penetration of polymer molecules into clay layers. Crystallinity, γ crystalline percentage and total molecular orientation of composite fibers were higher in comparison to neat nylon-6 fibers, as revealed by WAXD and birefringence measurements. Tensile strength of composite fibers was lower when compared to neat nylon-6 fibers. This may be attributed to some aggregation of nanoclay and its weakening effect. Melting and glass transition temperature of composite fiber was decreased due to the addition of modified nanoclay, indicating the formation of γ crystals and also breaking of some hydrogen bonds between the polymer molecules and the formation of new hydrogen bonds between the modified clay and the polymer molecules.