By E. Martuscelli, P. Musto, G. Ragosta
This quantity includes ten contributions which jointly supply an account of some of the techniques used to enhance the sturdiness of polymer matrices. The correlations one of the molecular constitution of the parts, the morphology, and the mechanical homes of combination structures are emphasised, as are the equipment used to manage the constitution of those fabrics in the course of processing. a few themes, that are integral within the layout and formula of difficult polymer blends, contain the function of the interface in multicomponent structures, the chemical reactivity of the combination parts, the mode and kingdom of dispersion of the second one part, the crystallinity and crystallization stipulations, and the glass transition temperature. additionally coated is the paintings which started within the early Seventies with the chemical amendment of ethylene-propylene copolymers for use as tougheners of Polyamide-6. Double-spaced. B&w illustrations.
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Extra resources for Advanced Routes for Polymer Toughening
27 The fact that the number of epoxy groups consumed is about twice the number of carbonyl groups seems to indicate that PC chain-seission occurs preferentially through the reaction scheme A. In any ease the formation of structures of type I is extremely important in the subsequent curing processes; in fact the epoxy functionalities at the end of the PC chains will take part in the crosslinking reactions, thus incorporating PC backbones within the epoxy network. After the high-temperature dissolution of PC in the epoxy matrix, the hardener MNA and the accelerator BDMA, were added in the desired proportions.
A,,), 1740 c m "1 (Vc_o, ester), 1454 cm -l (8c~,) , 1398 cm -1 (wcx,) 1267 cm -1 (Vc_o + Vc_c) and 1178, 1155, 1127 cm -l (vr [36,37]. To follow the conversion of the anhydride groups we monitored the intensity decrease of the well-resolved absorption at 1857 cm "1. From the spectral data it is readily possible to calculate the fractional conversion, ct, of the anhydride groups. The tz versus time curves for the pure epoxy resin (curve A) and for the B 15 blend (curve B) are reported in Fig. 12.
To follow the conversion of the anhydride groups we monitored the intensity decrease of the well-resolved absorption at 1857 cm "1. From the spectral data it is readily possible to calculate the fractional conversion, ct, of the anhydride groups. The tz versus time curves for the pure epoxy resin (curve A) and for the B 15 blend (curve B) are reported in Fig. 12. 6 ' A I ..... O'r 0 ' J ..... 100 I 200 . . 800 time (mirO Figure 12. 4) and for the B15 blend (curve B). The continuous lines represent the zero order fit; the dotted lines represent the first order fit.