scholarly journals Synthesis of Polyamide-6/Montmorillonite Nanocomposites by Direct In-situ Polymerization Catalysed by Exchanged Clay

2013 ◽  
Vol 29 (4) ◽  
pp. 1429-1436 ◽  
Author(s):  
Djamal Kherroub ◽  
Mohammed Belbachir ◽  
Saad Lamouri ◽  
Larbi Bouhadjar ◽  
Karim Karim Chikh
Keyword(s):  
In Situ Polymerization ◽  
Polyamide 6 ◽  
Montmorillonite Nanocomposites

Polyethylene-montmorillonite nanocomposites obtained by in situ polymerization of ethylene with nickel-diimine catalysts

2011 ◽  
Vol 122 (3) ◽  
pp. 2159-2165 ◽  
Author(s):  
Marcelo Luis Mignoni ◽  
Jonathan Vaz Martins Silva ◽  
Michèle Oberson de Souza ◽  
Raquel dos Santos Mauler ◽  
Roberto Fernando de Souza ◽  
...  
Keyword(s):  
In Situ Polymerization ◽  
Montmorillonite Nanocomposites

Crystallization Behavior of Polyethylene/Montmorillonite Nanocomposites Prepared by In Situ Polymerization

2012 ◽  
Vol 184-185 ◽  
pp. 932-935
Author(s):  
Min Li ◽  
Li Guang Xiao ◽  
Hong Kai Zhao
Keyword(s):  
Differential Scanning Calorimetry ◽  
Crystallization Behavior ◽  
Crystallization Process ◽  
In Situ Polymerization ◽  
Nucleating Agent ◽  
Lower Content ◽  
Melting Points ◽  
Scanning Calorimetry ◽  
Montmorillonite Nanocomposites

Polyethylene/montmorillonite (PE/MMT) nanocomposites were prepared by in situ polymerization. The crystallization behavior of PE/MMT nanocomposites at different MMT concentrations (from 0.1 to 1.2 wt %) were investigated by differential scanning calorimetry (DSC). The equilibrium melting points increase by the addition of MMT. The crystallization rates of PE/MMT nanocomposites are faster than those of pure PE. The addition of MMT facilitated the crystallization of PE, with the MMT functioning as a heterogeneous nucleating agent at lower content; at higher concentrations, however, the physical hindrance of the MMT layers to the motion of PE chains retarded the crystallization process.

scholarly journals PA6 and Halloysite Nanotubes Composites with Improved Hydrothermal Ageing Resistance: Role of Filler Physicochemical Properties, Functionalization and Dispersion Technique

Polymers ◽  
2020 ◽  
Vol 12 (1) ◽  
pp. 211 ◽  
Author(s):  
Valentina Sabatini ◽  
Tommaso Taroni ◽  
Riccardo Rampazzo ◽  
Marco Bompieri ◽  
Daniela Maggioni ◽  
...  
Keyword(s):  
Physicochemical Properties ◽  
Polymer Matrix ◽  
In Situ Polymerization ◽  
Cost Effective ◽  
Polyamide 6 ◽  
Halloysite Nanotubes ◽  
Amide Bonds ◽  
Molecular Weights ◽  
Dispersion Technique

Polyamide 6 (PA6) suffers from fast degradation in humid conditions due to hydrolysis of amide bonds, which limits its durability. The addition of nanotubular fillers represents a viable strategy for overcoming this issue, although the additive/polymer interface at high filler content can become privileged site for moisture accumulation. As a cost-effective and versatile material, halloysite nanotubes (HNT) were investigated to prepare PA6 nanocomposites with very low loadings (1–45% w/w). The roles of the physicochemical properties of two differently sourced HNT, of filler functionalization with (3-aminopropyl)triethoxysilane and of dispersion techniques (in situ polymerization vs. melt blending) were investigated. The aspect ratio (5 vs. 15) and surface charge (−31 vs. −59 mV) of the two HNT proved crucial in determining their distribution within the polymer matrix. In situ polymerization of functionalized HNT leads to enclosed and well-penetrated filler within the polymer matrix. PA6 nanocomposites crystal growth and nucleation type were studied according to Avrami theory, as well as the formation of different crystalline structures (α and γ forms). After 1680 h of ageing, functionalized HNT reduced the diffusion of water into polymer, lowering water uptake after 600 h up to 90%, increasing the materials durability also regarding molecular weights and rheological behavior.

scholarly journals The Effect of the Parameters of T-RTM on the Properties of Polyamide 6 Prepared by in Situ Polymerization

Materials ◽  
2019 ◽  
Vol 13 (1) ◽  
pp. 4 ◽  
Author(s):  
Orsolya Viktória Semperger ◽  
András Suplicz
Keyword(s):  
Mechanical Properties ◽  
Automotive Industry ◽  
Cycle Time ◽  
In Situ Polymerization ◽  
Rapid Development ◽  
Polyamide 6 ◽  
Raw Material ◽  
Short Cycle ◽  
Short Cycle Time

With the rapid development of the automotive industry, there is also a significant need to improve the raw materials used. Therefore, the demand is increasing for polymer composites with a focus on mass reduction and recyclability. Thermoplastic polymers are preferred because of their recyclability. As the automotive industry requires mass production, they require a thermoplastic raw material that can impregnate the reinforcement in a short cycle time. The most suitable monomer for this purpose is caprolactam. It can be most efficiently processed with T-RTM (thermoplastic resin transfer molding) technology, during which polyamide 6 is produced from the low-viscosity monomer by anionic ring-opening (in situ) polymerization in a tempered mold with a sufficiently short cycle time. Manufacturing parameters, such as polymerization time and mold temperature, highly influence the morphological and mechanical properties of the product. In this paper, the properties of polyamide 6 produced by T-RTM are analyzed as a function of the production parameters. We determine the crystallinity and the residual monomer content of the samples and their effect on mechanical properties.

Features of forming the structure and properties of polyamide-6 via in situ polymerization with oxidized graphite

2020 ◽  
Vol 27 (9) ◽  
Author(s):  
Dmitriy Leonov ◽  
Tatiana Ustinova ◽  
Natalia Levkina ◽  
Anton Mostovoy ◽  
Marina Lopukhova
Keyword(s):  
In Situ Polymerization ◽  
Polyamide 6 ◽  
Structure And Properties ◽  
Oxidized Graphite

scholarly journals Characterization of Polyamide 6/Multilayer Graphene Nanoplatelet Composite Textile Filaments Obtained Via In Situ Polymerization and Melt Spinning

Polymers ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 1787
Author(s):  
Jelena Vasiljević ◽  
Andrej Demšar ◽  
Mirjam Leskovšek ◽  
Barbara Simončič ◽  
Nataša Čelan Korošin ◽  
...  
Keyword(s):  
Melt Spinning ◽  
In Situ Polymerization ◽  
Complex Viscosity ◽  
Polyamide 6 ◽  
High Dispersion ◽  
Multilayer Graphene ◽  
Main Challenge ◽  
Dispersion State ◽  
Continuous Filament

Studies of the production of fiber-forming polyamide 6 (PA6)/graphene composite material and melt-spun textile fibers are scarce, but research to date reveals that achieving the high dispersion state of graphene is the main challenge to nanocomposite production. Considering the significant progress made in the industrial mass production of graphene nanoplatelets (GnPs), this study explored the feasibility of production of PA6/GnPs composite fibers using the commercially available few-layer GnPs. To this aim, the GnPs were pre-dispersed in molten ε-caprolactam at concentrations equal to 1 and 2 wt %, and incorporated into the PA6 matrix by the in situ water-catalyzed ring-opening polymerization of ε-caprolactam, which was followed by melt spinning. The results showed that the incorporated GnPs did not markedly influence the melting temperature of PA6 but affected the crystallization temperature, fiber bulk structure, crystallinity, and mechanical properties. Furthermore, GnPs increased the PA6 complex viscosity, which resulted in the need to adjust the parameters of melt spinning to enable continuous filament production. Although the incorporation of GnPs did not provide a reinforcing effect of PA6 fibers and reduced fiber tensile properties, the thermal stability of the PA6 fiber increased. The increased melt viscosity and graphene anti-dripping properties postponed melt dripping in the vertical flame spread test, which consequently prolonged burning within the samples.

Study of the Proper Sintering Conditions of Anionically-Polymerized Polyamide 6 Matrices for the Fabrication of Greencomposites

2012 ◽  
Vol 713 ◽  
pp. 121-126
Author(s):  
A. Alfonso ◽  
J. Andrés ◽  
J.A. García
Keyword(s):  
Material Characterization ◽  
Mechanical Performance ◽  
In Situ Polymerization ◽  
Research Work ◽  
Polyamide 6 ◽  
Liquid Composite Molding ◽  
Thermoplastic Matrix ◽  
Composite Molding ◽  
Long Fiber Thermoplastic

The present research work assesses the manufacture of long fiber thermoplastic matrix composite materials (GreenComposites). Thermoplastic matrices are too viscous to be injected into the conventional LCM (Liquid Composite Molding) molds, and then epoxy, polyester or vinylester resins are used. Nevertheless, the groundbreaking anionic polymerization of caprolactam allows such a synthesis of a thermoplastic APA6 matrix inside the mold. This matrix is sintered from the starting monomers, and presents high mechanical performance and recyclability. In order to do the reactive injection in a LCM mold, it is necessary to control the polymerization mechanism of such a thermoplastic matrix. This paper puts special emphasis on detecting and solving all problems which arose during synthesis. For instance, moisture values were assessed for all starting reactants, since humidity keeps polymerization from occurring. It is thought that once the synthesis and the resulting material characterization are well controlled, the manufacture of GreenComposites through in situ polymerization, as well as addition of state-of-the-art fabrics such as basalt, can proceed successfully.

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