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Influence on crystallinity

The properties of the nylons are considerably affected by the amount of crystallisation. Whereas in some polymers, e.g. the polyacetals and PCTFE, processing conditions have only a minor influence on crystallinity, in the case of the nylons the crystallinity of a given polymer may vary by as much as 40%. Thus a moulding of nylon 6, slowly cooled and subsequently annealed, may be 50-60% crystalline, while rapidly cooled thin-wall mouldings may be only 10% crystalline. [Pg.489]

Figure 10.1 shows the effect of the addition of fillers to polypropylene on its crystallinity. This study was conducted under the same conditions for all specimens tested. There is a difference in the effect of CaCO-, and talc. Calcium carbonate lacks surface functional groups so it tends to have a very small influence on crystallinity and the crystallization behavior. Talc has interacting functional groups on its surface which cause the increase in crystallinity along with the concentration increase. [Pg.486]

Chaudhary, D. S., Prasad, R., Gupta, R. K., and Bhattacharya, S. N. 2005. Clay intercalation and influence on crystallinity of EVA-based clay nanocomposites. Thermochimica Acta 433 187-195. [Pg.323]

The configuration of the chiral centers in the polymer chain has great influence on crystallinity. The crystal and... [Pg.71]

The decline in crystallinity is accompanied by an increase in the polyethylene lattice spacing 139,140), due to the influence of the skfc groups on the packing of chains. Ethyl branches have more influence on crystallinity than do methyl branches (49,139,140). [Pg.116]

A similar study was conducted by Paukkeri and Lehtinen [201], who proved that for molecular masses, Mw, ranging from 2.2 x 10 to 9.5 x 10, isotacticity was the main parameter determining crystallization peak temperature and crystallinity, whereas the molecular mass had a much less pronounced effect on the crystallization rate, and almost no influence on crystallinity. Moreover, in contrast with the flndings of Burfield el al. [200], very small differences between the samples produced with different processes and catalysts were reported. [Pg.241]

One of the most important characteristics that predominantly determines the properties and the behavior of different grades of PE is their branching which influences the ability of the polymer to crystallize. The nature, size, and distribution of branches have a dominant influence on crystallinity, density and consequently on mechanieal properties (Fig. 96). [Pg.274]

Keith H D and Paddeii F J Jr (1964) Spherulitic crystallization from the melt. I. Fractionation and impurity segregation and their influence on crystalline morphology, J Appl Phys 35 1270-1285. [Pg.66]

New lonomer Types. There is a continuing interest in new ionomers within the academic community, since novel and unexpected phenomena are frequently being discovered. However, there are still many unanswered questions with respect to the ethylene ionomers, especially the influence of ionic bonding on crystalline stmcture. Continued study of these interesting polymers will close the gaps in knowledge of this area of polymer science. [Pg.409]

Some limestones, more often the coarse crystalline types, can never be calcined successfully. Such stone tends to decrepitate during preheating or calcination into fine particles that interfere with this pyrochemical reaction. The adaptabiflty of a stone for calcination can only be ascertained with surety by empirical methods. Possibly the greatest influence on lime quaflty is the size gradation of limestone. Narrow gradations, such as... [Pg.171]

A left-handed double-heUcal stmcture has been proposed for geUan in the crystalline state, based on x-ray diffraction studies (227). The presence of acetyl groups presumably dismpts interchain aggregation, since these groups are postulated to be on the outside of the heUces. The role played by acetyl and glyceryl ester groups and their influence on the double-heUcal stmcture has been studied using computet models (232). [Pg.299]

Mechanical Properties. The principal mechanical properties are Hsted in Table 1. The features of HDPE that have the strongest influence on its mechanical behavior are molecular weight, MWD, orientation, morphology, and the degree of branching, which determines resin crystallinity and density. [Pg.381]

Lu and Pizzi [83] showed that lignocellulosic substrates have a distinct influence on the hardening behavior of PF-resins, whereby the activation energy of the hardening process is much lower than for the resin alone [84]. The reason is a catalytic activation of the PF-condensation by carbohydrates like crystalline and amorphous cellulose and hemicellulose. Covalent bonding between the PF-resin and the wood, especially lignin, does not play any role [84]. [Pg.1056]

The low electrical conductivity of PET fibers depends essentially on their chemical constituency, but also to the same extent on the fiber s fine structure. In one study [58], an attempt was made to elucidate the influence of some basic fine structure parameters on the electrical resistivity of PET fibers. The influence of crystallinity (jc) the average lateral crystallite size (A), the mean long period (L), and the overall orientation function (fo) have been considered. The results obtained are presented in the form of plots in Figs. 9-12. [Pg.854]

The phase behavior of a-ester sulfonates has been studied in detail with methyl laurate and methyl palmitate [58]. In both cases, at higher temperatures, as the surfactant concentration increases, there is a transition from an isotropic solution to a hexagonal liquid crystalline phase and finally, at high surfactant concentrations, to a lamellar liquid crystal (Fig. 4). The crystal/liquid-crys-tal phase transition occurs at even higher temperatures as the chain length increases. On the other hand, chain length has practically no influence on the... [Pg.477]

For quantitative work, it is necessary to estimate the concentration of 5-amino-l-(P-D-ribofuranosyl)imidazole in aqueous solution. It seems that the only available method is the Bratton-Marshall assay, which was originally developed for the estimation of arylamines in biological fluids. The principle of the method is the spectrometric estimation of a salmon-pink colored dyestuff obtained by diazotation in situ, followed by coupling with /V-( 1 -naphthyl)ethyl-enediamine.65 The only remaining problem then is to know the molar extinction of this dye because pure samples of AIRs are not available. A value of 16800 at 520 nM was obtained for the dyes prepared from a model compound, 5-amino-l-cyclohexylimidazole-4-carboxylic acid (54), which is crystalline. A comparable molar extinction can be expected for the dye prepared from imidazole 55, if the carboxyl group does not exert too much influence on the chromophore. Actually, its influence is perceptible even with the naked eye, the dyestuff prepared from 53 having a somewhat different, wine-red color, with max>520 nM. The molar extinction for 55 is 17400 at 500 nM. When the decarboxylation of 54 was conducted under mild acidic conditions (pH 4.8, 50°C, 1 hour), estimation of 5-aminoimidazole 55 by the Bratton-Marshall method led to the conclusion that the reaction was almost quantitative.66 Similar conditions for the final decarboxylation were adopted in the preparation of samples of AIRs labeled with stable isotopes.58... [Pg.299]

Similarly, a composite of hydroxyapatite and a network formed via cross-linking of chitosan and gelatin with glutaraldehyde was developed by Yin et al. [ 169]. A porous material, with similar organic-inorganic constituents to that of natural bone, was made by the sol-gel method. The presence of hydroxyapatite did not retard the formation of the chitosan-gelatin network. On the other hand, the polymer matrix had hardly any influence on the high crystallinity of hydroxyapatite. [Pg.172]


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