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Wyszukujesz frazę "curing networks" wg kryterium: Temat


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Tytuł:
Research on the Mechanical Properties and Curing Networks of Energetic GAP/TDI Binders
Autorzy:
Ma, S.
Li, Y.
Li, G.
Luo, Y.
Tematy:
glycidyl azide polymer (GAP)
curing networks
hydrogen bonding
entanglement
integrity
Pokaż więcej
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
Powiązania:
https://bibliotekanauki.pl/articles/358300.pdf  Link otwiera się w nowym oknie
Opis:
This research focused on correlations between the macroscopic mechanical performance and microstructures of energetic binders. Initially a series of glycidyl azide polymer (GAP)/toluene diisocyanate (TDI) binders, catalyzed by a mixture of dibutyltin dilaurate (DBTDL) and triphenyl bismuth (TPB), was prepared. Uniaxial tensile testing, and low-field nuclear magnetic resonance and infrared spectroscopy were then used to investigate the mechanical properties, curing networks, and hydrogen bonding (H-bonds) of these binders. Additionally, a novel method based on the molecular theory of elasticity and the statistical theory of rubber elasticity was used to analyze the integrity of the networks. The results showed that the curing parameter R strongly influences the mechanical properties and toughness of the binders, and that a tensile stress (σm) of 1.6 MPa and an elongation (εm) of 1041% was observed with an R value of 1.6. The cross-linking density increased sharply with the curing parameter, but only modestly with an R value ≥ 1.8. The proportion of H-bonds formed by the imino groups increased with the R value and reached 72.61% at an R value of 1.6, indicating a positive correlation between the H-bonds and σm. Molecular entanglement was demonstrated to increase with R and to contribute dramatically to the mechanical performance. The integrity of these networks, evaluated by a correction factor (A), varies with R, and a network of the GAP/TDI binder with an R value of 1.6 is desirable.
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Radiation-induced cross-linking polymerization : recent developments for coating and composite applications
Autorzy:
Coqueret, Xavier
Tematy:
acrylate monomers
coating composite
cross-linking polymerization
polymer networks
V/EB curing
Pokaż więcej
Wydawca:
Instytut Chemii i Techniki Jądrowej
Powiązania:
https://bibliotekanauki.pl/articles/58906573.pdf  Link otwiera się w nowym oknie
Opis:
Radiation-initiated cross-linking polymerization of multifunctional monomers is an attractive method used for drying solvent-free liquid coatings, inks, and adhesive as well as for fabricating high-performance composite materials. The method offers a number of advantages compared with thermal curing processes. Free radical and cationic polymerization have been investigated in detail over the past years. A high degree of control over curing kinetics and material properties can be exerted by adjusting the composition of matrix precursors and/or by acting on the process parameters (overall dose, dose rate, dose increment, initial temperature). Several pending issues that require deeper investigations are as follows: (i) the fast polymerization of multifunctional monomers generates micro-heterogeneous networks requiring detailed characterization and quantifi cation by microscopic, thermal, and spectroscopic analyses; (ii) the adhesion and surface properties of radiation-cured coatings are quite sensitive to processing parameters; and (iii) signifi cant enhancement of the toughness is needed to qualify potential matrices based on simple difunctional monomers for high-performance composites. Recent results show that the bulk and surface properties of radiation-cured materials can be improved by advanced formulation of matrix precursors and by a parametric study of the processing factors.
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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