Rubber toughening of glass-fiber -reinforced nylon 66

Glass fibers are commonly added to thermoplastics by the process of extrusion compounding for a variety of reasons, mainly to enhance their strength and make them dimensionally stable. Since the extruder has to be flushed out each time product composition is changed, a large amount of incompatible polymeric waste is generated. This waste material is usually landfilled even though the polymers contained in it are valuable and worth being recycled. It is the drastic reduction in mechanical properties resulting from polymer incompatibility which restricts their recycling. A good strategy of recycling thermoplastics calls for separating materials from each other before utilizing them. This research deals with characterizing and rubber toughening of a post industrial glass-fiber-reinforced nylon 66 which was separated from other polymers. A virgin glass-fiber-reinforced nylon 66 was also used in order to compare its properties with those of the recycled ones.;Rubbers used in this study were Styrene-Ethylene-Butylene-Styrene and Ethylene-Propylene grafted with maleic anhydride; SEBS-g-MA and EP-g-MA. Composites of glass-fiber-reinforced nylon 66 with various rubber contents were prepared by extrusion. The pelletized extrudates were injection molded to different standard specimens for mechanical testing such as impact, tensile, and flexural. Flow properties of the composites were examined by the melt flow index and rotational viscometry. Morphology of the fractured surface of the composites was examined by scanning electron microscopy.;Elongation and impact strength of the composites were found to increase with increasing rubber content while tensile and flexural strength decrease with increasing rubber content. Elongation of the recycled material was slightly less than that of the virgin material. This is probably due to the presence of contaminants within the recycled material. The variation of rubber content with both tensile and flexural strengths was found to obey the rule of mixtures. The morphology of the fractured surfaces showed significant signs of plastic deformation such as shear bands and cavitations as rubber content increased, and this correlates well with mechanical properties which resulted in an increase in toughness of the composites when rubber content was increased. The results of this investigation clearly show the possibility of balancing strength and toughness of the material when adding rubber to a glass-fiber-reinforced nylon 66

Low-temperature synthesis method for the fabrication of efficient polymer-blend systems

It is essential that the particle sizes of polymer blends are controlled to ensure their superior properties. In this study, polymer blends at low temperatures were fabricated. Unlike conventional methods that use high temperatures, this method exhibited energy efficiency during melt processing and a polymeric product with appreciable mechanical properties was fabricated. A polystyrene/polyethylene terephthalate (PS/PET) blend system with 1–4 wt.% PET particles dispersed into the PS matrix at 180 °C was synthesized. The resulting PS/PET blends exhibited uniquely shaped PET dispersed phase and mechanical properties that were twice as high as that of the blends processed at a higher temperature of 290 °C. The proposed method is the first to incorporate polymeric fibers into another polymer matrix at a lower temperature, resulting in energy efficiency and superior mechanical properties

CCDC 1435119: Experimental Crystal Structure Determination

Related Article: Ashok Keerthi, Cunbin An, Mengmeng Li, Tomasz Marszalek, Antonio Gaetano Ricciardulli, Boya Radha, Fares D. Alsewailem, Klaus Müllen, Martin Baumgarten|2016|Polym.Chem.|7|1545|doi:10.1039/C6PY00023

Recyclable, strong thermosets and organogels via paraformaldehyde condensation with diamines

Nitrogen-based thermoset polymers have many industrial applications (for example, in composites), but are difficult to recycle or rework. We report a simple one-pot, low-temperature polycondensation between paraformaldehyde and 4,4′-oxydianiline (ODA) that forms hemiaminal dynamic covalent networks (HDCNs), which can further cyclize at high temperatures, producing poly(hexahydrotriazine)s (PHTs). Both materials are strong thermosetting polymers, and the PHTs exhibited very high Young's moduli (up to ∼14.0 gigapascals and up to 20 gigapascals when reinforced with surface-treated carbon nanotubes), excellent solvent resistance, and resistance to environmental stress cracking. However, both HDCNs and PHTs could be digested at low pH (&lt;2) to recover the bisaniline monomers. By simply using different diamine monomers, the HDCN- and PHT-forming reactions afford extremely versatile materials platforms. For example, when poly(ethylene glycol) (PEG) diamine monomers were used to form HDCNs, elastic organogels formed that exhibited self-healing properties.</p

Recyclable, strong thermosets and organogels via paraformaldehyde condensation with diamines

Nitrogen-based thermoset polymers have many industrial applications (for example, in composites), but are difficult to recycle or rework. We report a simple one-pot, low-temperature polycondensation between paraformaldehyde and 4,4′-oxydianiline (ODA) that forms hemiaminal dynamic covalent networks (HDCNs), which can further cyclize at high temperatures, producing poly(hexahydrotriazine)s (PHTs). Both materials are strong thermosetting polymers, and the PHTs exhibited very high Young's moduli (up to ∼14.0 gigapascals and up to 20 gigapascals when reinforced with surface-treated carbon nanotubes), excellent solvent resistance, and resistance to environmental stress cracking. However, both HDCNs and PHTs could be digested at low pH (<2) to recover the bisaniline monomers. By simply using different diamine monomers, the HDCN- and PHT-forming reactions afford extremely versatile materials platforms. For example, when poly(ethylene glycol) (PEG) diamine monomers were used to form HDCNs, elastic organogels formed that exhibited self-healing properties

Recyclable, strong thermosets and organogels via paraformaldehyde condensation with diamines

\u3cp\u3eNitrogen-based thermoset polymers have many industrial applications (for example, in composites), but are difficult to recycle or rework. We report a simple one-pot, low-temperature polycondensation between paraformaldehyde and 4,4′-oxydianiline (ODA) that forms hemiaminal dynamic covalent networks (HDCNs), which can further cyclize at high temperatures, producing poly(hexahydrotriazine)s (PHTs). Both materials are strong thermosetting polymers, and the PHTs exhibited very high Young's moduli (up to ∼14.0 gigapascals and up to 20 gigapascals when reinforced with surface-treated carbon nanotubes), excellent solvent resistance, and resistance to environmental stress cracking. However, both HDCNs and PHTs could be digested at low pH (&lt;2) to recover the bisaniline monomers. By simply using different diamine monomers, the HDCN- and PHT-forming reactions afford extremely versatile materials platforms. For example, when poly(ethylene glycol) (PEG) diamine monomers were used to form HDCNs, elastic organogels formed that exhibited self-healing properties.\u3c/p\u3

Computational Investigations on Base-Catalyzed Diaryl Ether Formation

We report investigations with the dispersion-corrected B3LYP density functional method on mechanisms and energetics for reactions of group I metal phenoxides with halobenzenes as models for polyether formation. Calculated barriers for ether formation from <i>para</i>-substituted fluorobenzenes are well correlated with the electron-donating or -withdrawing properties of the substituent at the <i>para</i> position. These trends have also been explained with the distortion/interaction energy theory model which show that the major component of the activation energy is the energy required to distort the arylfluoride reactant into the geometry that it adopts at the transition state. Resonance-stabilized aryl anion intermediates (Meisenheimer complexes) are predicted to be energetically disfavored in reactions involving fluorobenzenes with a single electron-withdrawing group at the <i>para</i> position of the arene, but are formed when the fluorobenzenes are very electron-deficient, or when chelating substituents at the <i>ortho</i> position of the aryl ring are capable of binding with the metal cation, or both. Our results suggest that the presence of the metal cation does not increase the rate of reaction, but plays an important role in these reactions by binding the fluoride or nitrite leaving group and facilitating displacement. We have found that the barrier to reaction decreases as the size of the metal cation increases among a series of group I metal phenoxides due to the fact that the phenoxide becomes less distorted in the transition state as the size of the metal increases