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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 18 (1955), S. 491-495 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A study of the dynamic mechanical properties of several high polymers has been made over a temperature range from 80°K. to above room temperatures and at frequencies in the range from 200 to 4000 cps. For amorphous polymers such as polystyrene the mechanicalloss rises sharply in the neighborhood of 80°C. but over the rest of the temperature range studied exhibits no relaxation peaks. For partly crystalline polymers such as polymethylene, polytetrafluoroethylene, and nylon the loss curve exhibits one or more definite internal friction peaks in the temperature range studied. The observed relaxation behavior is discussed in terms of possible molecular mechanisms and the results correlated with specific heat measurements and other mechanical loss measurements where such data are available.
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 22 (1956), S. 455-462 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of chain branching on the dynamic mechanical properties of polyethylene within the temperature region 80 to 380°K. has been studied using an apparatus which drives rod-like specimens in their transverse modes. The results for three types of polyethylene having 3.2, 1.6, and less than 0.1 branches per 100 carbon atoms of the main chain are compared and discussed. Experimental results indicate that all of the three main dispersion regions (α, β, γ) characteristic of polyethylene are affected to some extent by branching. The β region, starting near 230°K., decreases with decreased branching, and for polyethylene which has negligible branching it is almost entirely absent. This suggests a direct relation between the number of branch points and the size and shape of this peak. The γ dispersion region near 170°K. appears sharper and shifted to higher temperatures with decreased branching, this being attributed to a narrowing of the relaxation times associated with the movement of a small number of CH2 units. The α dispersion region near 370°K. is also shifted to higher temperatures with decreased branching in accord with the shift of melting temperature with degree of crystallinity.
    Additional Material: 4 Ill.
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  • 3
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effects of pile irradiation on the damping and resonant frequency of a “high pressure” polyethylene has been investigated over a temperature range from 80 to 550°K. in the audiofrequency region using an apparatus which drives rod-like specimens in their transverse modes. Using irradiation dosages which result in approximately 4% crosslinking or greater, the mechanical loss peaks found at about 165, 265, and 355°K. in polyethylene are altered. Definite changes in the resonant frequency or modulus-temperature plots also occur. The 355°K. peak, attributed to the melting of the crystalline portions of the sample, decreases in height and shifts to lower temperatures with increasing irradiation dose. A decrease in the height of the 265°K. peak accompained by a shift to higher temperatures takes place. The 165°K. peak initially increases in height and peak temperature but at higher dosages a marked decrease in the damping maximum occurs. The damping behavior in the 165 and 265°K. regions is discussed in terms of diffusional motion of chain segments in the amorphous polymer portions.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 25 (1957), S. 381-384 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 5
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 6
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Proton magnetic resonance of a number of polyamides has been investigated in the 80-410°K. range. Line width and second moment vs. temperature plots for dry specimens of poly(hexamethylene adipamide) and poly(hexamethylene sebacamide) are found to exhibit two transition regions. Saturation with H2O or D2O lowers the temperature of the principal line-narrowing process for the above two polymers as well as for poly(decamethylene sebacamide) and shifts part of the second-moment transition which occurs above room temperature to lower temperatures; in both cases H2O has a more pronounced effect than D2O. Exchange of the protons, presumably on the amide groups, for deuterium leads to small decreases in line width and second moment at temperature in and below the main transition. N-methylation of poly(decamethylene sebacamide) up to 58% causes marked shifts of the principal line-narrowing process and NMR second moment transition to lower temperatures. The NMR data are found to be in qualitative agreement with dynamic mechanical measurements on similar samples.
    Additional Material: 8 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 26 (1957), S. 383-386 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 8
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The damping, resonant frequency, and dynamic elastic storage modulus of five polyamides have been investigated at resonant frequencies ranging from 100 to 2000 cycles/sec. at temperatures in the 100 to 450°K. region. Specimens of poly(hexamethyleneadipamide) containing 0, 0.9, 3.3, and 6.4 wt.-% water were studied and it was found that with increasing water content: the loss peak and associated modulus dispersion at 170°K. in the dry material decreased; the loss peak and modulus dispersion at 370°K. in the dry material shifted to lower temperatures reaching a value of 280°K. for 6.4% water; a third damping peak appeared at 240 to 245°K. and the modulus in the 150 to 250°K. region increased while above and below this range the reverse was true. A poly(hexamethylene adipamide) specimen containing 10.5 wt.-% methanol exhibited one broad peak at about 255 to 260°K. Dry specimens of poly(hexamethylene sebacamide), poly(decamethylene sebacamide), 17% N-methylated poly(decamethylene sebacamide), and 58% N-methylated poly(decamethylene sebacamide) were also investigated. For the latter three specimens the principal amorphous transition shifted from 340 to 285°K. and the area under the loss peak increased greatly in going from 0 to 58% N-methylation, while the low temperature transition remained at 160 to 170°K. essentially unchanged. Of the five polymers studied the 17% N-methylated poly(decamethylene sebacamide) exhibited the highest apparent modulus in the 110 to 160°K. region; and at all temperatures below the principal amorphous transition this material had a higher modulus than the unmethylated parent polymer.
    Additional Material: 6 Ill.
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  • 9
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Internal friction (Q-1) and dynamic elastic storage modulus have been measured as functions of temperature (80°K. and higher) for partially crystalline samples of poly(pentene-1) (PP1), poly(3-methylbutene-1), (P3MB1), and poly(4-methylpentene-1) (P4MP1); a resonance technique at audiofrequencies was used. Two internal friction peaks at 145°K. (γ) and 290°K. (β) and a final upswing in Q-1 at 335-345°K. (α) in conjunction with associated modulus dispersions are exhibited by PP1, the mechanical loss spectrum being similar to that reported previously for poly(butene-1) except that the final upswing for PP1 occurs at lower temperatures. Both P3MB1 and P4MP1 have small Q-1 damping peaks near 150°K. (γ). The latter polymer also has a peak of considerable magnitude at 335-340°K. (β) and an upswing in Q-1 at 425-435°K. (α). The former polymer shows a broad dispersion commencing at about 320°K. (β). Owing to the absence of a sizable transition below the principal amorphous transition starting at about 325°K., the modulus for P3MB1 exhibits the least variation with temperature in the range of 80-325°K. among the poly-α-olefins with aliphatic side chains, including polyethylene and polypropylene, that have been studied by this method. It is suggested that the γ and β loss peaks and associated modulus changes are the consequence of the onset of motion in the amorphous regions, involving small and large number of chain segments, respectively.
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 58 (1962), S. 19-28 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The internal friction and the dynamic modulus of isotactic polypropylene samples subject to varying degrees of pile irradiation have been studied at low audio frequencies and over the temperature range from 100°K. to over 400°K. The radiation dosages used varied from 5.4 × 1017 to 14 × 1018 nvt. For irradiation doses up to about 3 × 1018 nvt, one observed change is a decrease in the temperature at which the final upswing in damping and drop in modulus occurs, presumably as a result of defects produced in the crystallites by the irradiation. As the irradiation dose increases above 3 × 1018 nvt, all evidence of crystallinity is lost, and the internal friction peak which occurs in the neighborhood of 300°K. and which is associated with the glass transition of the amorphous regions moves to higher temperatures as a result of the increasing chainstiffening effect due to crosslinking. The secondary loss peak at 250°K. attributed to the motion of a small number of segments in the amorphous regions is found to increase in magnitude with increasing dose. The results of density determinations made before and after irradiation and also after subsequent exposure of the irradiated samples to melting temperatures and of solvent extraction studies of the irradiated samples confirm the simultaneous occurrence of crosslinking and of crystalline degradation upon pile irradiation of polypropylene samples.
    Additional Material: 4 Ill.
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