Comparison of nanocomposites based on nylon 6 and nylon 66

Nylon 6 and nylon 6,6 organoclay nanocomposites were prepared by melt processing using a twin screw extruder. The effects of polyamide type and processing temperature on the mechanical properties and the morphology of the nanocomposites were examined. Mechanical properties, transmission electron microscopy (TEM), wide-angle X-ray diffraction (WAXD), percentage crystallinity and isothermal thermo-gravimetric analysis (TGA) data are reported. A particle analysis was performed to quantitatively characterize the morphology; these results are later employed in modeling the modulus of these materials using composite theory. No significant difference was observed in the mechanical properties and morphology of PA-6 nanocomposites processed at two different temperatures. PA-6 nanocomposites had superior mechanical properties than those made from PA-66. The tensile strength of PA-66 nanocomposites deviated from linearity at high levels of MMT. WAXD and TEM results show that the PA-6 nanocomposites are better exfoliated than the PA-66 nanocomposites, which exhibit a mixture of intercalated and exfoliated structures. Mechanical properties were consistent with the morphology. DSC reveals a higher percentage of crystallinity in the PA-66 samples. Isothermal TGA shows only a 5% difference in the degradation of the organic modifier on the organoclay processed at 240 °C versus 270 °C. Particle analysis shows a higher average particle length and thickness, and a lower average particle density and aspect ratio in nanocomposites based on PA-66 versus PA-6. The Halpin-Tsai and Mori-Tanaka composite theories predict satisfactorily the behavior of the PA-6 nanocomposites, while the PA-66 nanocomposites were predicted acceptably up to a certain volume fraction where the non-linear behavior takes effect. All the results indicate that there is a lower degree of exfoliation in the nanocomposites produced with a PA-66 matrix apparently stemming from the chemical differences between PA-6 and PA-66.     

Polyamides incorporating furan moieties. 5. Synthesis and characterisation of furan-aromatic homologues

2,2′-Bis (5-chloroformyl 2-furyl) propane and various aromatic diamines were used as monomers in the study of their interfacial polycondensation and the properties of the ensuing furanic-aromatic polyamides. The effects of such variables as the nature of the organic phase, the temperature, the reaction time, and the type and concentration of the catalyst were investigated as well as the properties of the polyamides in terms of structure, average chain length, T_g, T_m and thermal stability.     

Effect of polar solvents on the crystalline phase of polyamides

We investigate the effect of absorption of polar solvents (water and ethanol) on the structure of amorphous and semi-crystalline copolyamides containing aromatic entities. Different length scales of structural organisation are probed using a combination of Small angle X-ray scattering and neutron/X-rays diffraction. Crystallisation in the presence of solvent, characterised by very slow kinetics, is observed in the originally amorphous material, as a combined effect of a rearrangement of the hydrogen-bond distribution and plasticization. The steady-state crystalline structure is reached on a timescale much longer than the absorption kinetics, and is similar but not identical to that of processed semi-crystalline materials. In semi-crystalline polyamides water absorption induces a swelling of the spacing of the lamellar stacking but also modifications of the unit cell structure, which suggest a moderate but significant rearrangement of the hydrogen bond structure in the crystalline phase.     

Ionic liquid catalyzed synthesis of organosoluble wholly aromatic optically active polyamides

A series of optically active wholly aromatic polyamides (PAs) with amino acid moieties in the pendant groups have been synthesized through polycondensation of a chiral diacid and aromatic diamines in an ionic liquid (IL) as a green, safe and eco-friendly medium and also reactions catalysis agent (method I). Furthermore, the polymerization reactions were performed via conventional polycondensation (method II) and obtained results have been compared. Evaluation of data shows that IL is the better polyamidation medium and catalysis stand on the higher inherent viscosities and yields of the obtained PAs and the rate of polymerizations beyond the greener reaction conditions and deletion of some essential reagents in conventional manners. Characterization were performs by means of ¹H-NMR and FT-IR spectroscopy, elemental analysis, thermogravimetric analysis and differential scanning calorimetric techniques.     

Acylated and hydroxylated polyamides derived from l-tartaric acid

A series of polyamides 6,4 were prepared from 1,6-hexanediamine and active esters of 2,3-di-O-acylated l-tartaric acid by polycondensation in solution. Both O-alkoyl and O-benzoyl esters were used as hydroxyl protecting groups. The resulting acylated polytartaramides were found to be semicrystalline polymers with T_m between 100 and 200 °C and T_g slightly above 100 °C. Controlled hydrolysis of the ester side group led to the preparation of poly(hexamethylene l-tartaramide)s with different content in free hydroxyl groups. These polyamides continue being crystalline but their properties largely differ from those displayed by their parent acylated polymers.     

Dimer acid-based thermoplastic bio-polyamides: Reaction kinetics, properties and structure

New dimer acid-based-polyamides were synthesized with rapeseed oil-based dimer acid (DA) and 1,2-diaminoethane, 1,6-diaminohexane or 1,8-diaminooctane to form DAPAe, DAPAh and DAPAo, respectively. Effects of diamine chain lengths on kinetics evolution as well as on the thermal, physical and mechanical properties of the different polyamides synthesized were investigated. DAPAo was found to be the most reactive diamine because of its higher nucleophilic character. Differential scanning calorimetry (DSC) combined with X-ray diffraction revealed a low-order semi-crystalline structure for all polyamides. A tentative schema for the structural organization of these DAPA is proposed and shows a specific organization with local semi-crystalline segregation domains. DAPAe was found to possess the higher melting temperature likely due to higher crystal cohesion, which was confirmed by higher Young modulus in stress-strain experiments. Rheological data showed an increase of the glass transition temperature concomitantly with the increase of diamine chain length. They also revealed an increase of complex viscosity with the diamine chain length. Investigation of thermal stability showed that DAPAe degrades before DAPAh and DAPAo in connection with the number of methylene units per diamine.     

Corrosion protective performances of commercial low-VOC epoxy/urethane coatings on hot-rolled 1010 mild steel

The protective properties of low-VOC epoxy/urethane paint systems of commercial grade have been investigated using a variety of techniques such as electrochemical impedance spectroscopy (EIS). One epoxy-polyamide mastic/urethane, three high-solid epoxy-amine/urethane coatings, one solvent-free epoxy-amine/urethane, one water-based epoxy-amine and one high-VOC alkyd paint system (used as paint reference system) were applied on hot-rolled 1010 mild steel panels and exposed for up to 2000 h in the salt spray cabinet (SSC) or for 1 year at an outdoor marine test site. These paints were tested for their barrier properties, corrosion-induced adhesion loss and visual defects, as well as for their flexibility and resistance to direct impact. The barrier properties increased in the following order: alkyd相似文献   

A kinetic study of the reduction of chromium(VI) to chromium(III) by thiourea

The reduction of chromium(VI) to chromium(III) by thiourea is a key aspect of the chromium(VI)–thiourea–polyacrylamide gel polymer system used in oil recovery processes. A study was undertaken to develop a kinetic model for the reduction reaction. Reaction mixtures were prepared and chromium(VI) concentrations were determined from the mixtures's visible absorbance. The reaction rate was found to depend on the concentrations of chromium(VI), thiourea, and polyacrylamide and on solution pH. A kinetic model for the reactions was developed using the experimental data and previously proposed reaction mechanisms. The model accurately predicts the reaction rate in solutions that do not contain polyacrylamide and predicts a rate that is approximately correct for solutions containing polyacrylamide.     

Co-phase continuity in immiscible binary polymer blends

Methods of microscopic observation and macroscopic characterization have been developed for determining the co-phase continuity in immiscible binary blends. After selective dissolution of the component polymers, the morphologies of microscopic observation are consistent with the results of macroscopic observation and weight percentage determination. By using these methods, the relationship between co-phase continuity, composition and blending time has been explored for two immiscible binary polyblends with different viscosity ratios (λ), polyamide 6/polyethersulfone (PA/PES, λ = 0.03) and poly(butylene terephthalate)/polystyrene (PBT/PS, λ = 1). Both blend systems show a similar dependence of co-phase continuity on the composition and mixing time. That is at short mixing time (for example, 2 minutes), the co-phase continuity takes place in a wide composition range. With increasing blending time, the composition range of co-phase continuity becomes narrow, and finally shrinks to one point. After a long enough mixing time the co-phase continuity region will occur only at a volume fraction of

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, no matter what the viscosity ratio of the blend is. © 1997 Elsevier Science Ltd.     

Crystallization behavior of polymer/montmorillonite nanocomposites. Part III. Polyamide-6/montmorillonite nanocomposites, influence of matrix molecular weight, and of montmorillonite type and concentration

Several series of polyamide-6 (PA-6) nanocomposites, differing in montmorillonite (MMT) type and content and PA-6 matrix molecular weight, were prepared by melt-extrusion and the associated PA-6 crystallization behavior and morphology was evaluated using (synchrotron) X-ray diffraction, transmission electron microscopy and differential scanning calorimetry. The nucleating ability of silicate layers is poor in PA-6 nanocomposites made by melt-extrusion because highly active, stable PA-6 crystallization precursors are generated during melt-extrusion. In most of the studied PA-6/MMT nanocomposites the dispersed silicate layers act as impurities and decrease rather than increase the overall crystallization kinetics of PA-6, especially at high MMT contents. Furthermore, at a given MMT concentration, the crystal growth retardation inflates with increasing degree of exfoliation, which dependents on the MMT type and which increases with increasing PA-6 molecular weight. One of the considered MMT types leads to a poorly exfoliated nanomorphology and as a result no retardation of crystal growth is observed. Furthermore, the disturbed crystal growth does not alter the PA-6 semicrystalline stack morphology. Moderate nucleation effects due to the presence of MMT can be observed when the particle load is low (low amount of MMT and/or poor degree of exfoliation) and provided the supercooling is sufficiently large.