Journal of Materials Science

, Volume 22, Issue 5, pp 1707–1714 | Cite as

Stress cracking of nylon polymers in aqueous salt solutions

Part 1 Stress-rupture behaviour
  • Michael G. Wyzgoski
  • Glen E. Novak
Article

Abstract

The susceptibility of nylon polymers to environmental stress cracking in aqueous salt solution was investigated. The time to fail (complete rupture) was recorded for razor-cut precracked samples which were totally immersed in water, sodium chloride, or calcium chloride at various initial stress intensity levels and temperatures. Ductile failures were observed in both water and aqueous sodium chloride at all temperatures. However, in saturated aqueous calcium chloride the nylon failure mode changed from ductile tearing, at room temperature, to crazing and crachng at elevated temperatures (50 to 100° C). Lithium and magnesium chlorides were also observed to be potent cracking agents at the elevated temperatures. The temperature interval over which cracking occurred corresponded to the onset of the Oass transition temperature,Tg of the nylon. Thus, nylon 6, having a lowerTg, was more susceptible to cracking than nylon 6,6 et any given temperature. [)n the other hand' nylon 11, having a lower ratio of amide tornathy!onegroups, wasnotuuuoaptib!eto salt-induced cracking, For the nylon 6 and nylon 6,6 the failure kinetics in salt solutions were similar, regardless of whether dry samples or previously moisturized samples were examined. Thus e simple tempmra1ure-moisture content equivalence does not apply forsalt-induced stress cracking in aqueous solutions.

Keywords

Lithium Sodium Chloride Elevated Temperature Nylon Stress Intensity 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    C. D. Weiske,Kuntstoffe 54 (1964) 626.Google Scholar
  2. 2.
    P. Dunn andG. F. Sansom,J. Appl. Polym. Sci. 13 (1969) 1641.Google Scholar
  3. 3.
    Idem, ibid. 13 (1969) 1657.Google Scholar
  4. 4.
    Idem, ibid. 13 (1969) 1673.Google Scholar
  5. 5.
    Idem, ibid. 14 (1970) 1799.Google Scholar
  6. 6.
    M. G. Wyzgoski in “Macromolecular Solutions: Solvent Property Relationships in Polymers”, edited by R. B. Seymour and G. A. Stahl (Pergamon, New York, 1982) p. 41.Google Scholar
  7. 7.
    A. C. Reimschuessel andY. J. Kim,J. Mater. Sci. 13 (1978) 243.Google Scholar
  8. 8.
    R. P. Burford andD. R. G. Williams,ibid. 14 (1979) 2872.Google Scholar
  9. 9.
    R. P. Burford andE. Harraver,Polymer 2 (1983) 1001.Google Scholar
  10. 10.
    H. Kim andP. J. Harget,J. Appl. Phys. 50 (1979) 6072.Google Scholar
  11. 11.
    A. Siegmann andZ. Baraam,Makromol. Chem., Rapid Commun. 1 (1980) 113.Google Scholar
  12. 12.
    M. I. Koran, “Nylon Plastics” (Wiley, New York, 1973) p. 329.Google Scholar
  13. 13.
    W. F. Brown Jr andJ. E. Srawley, “Plane Strain Crack Toughness Testing of High Strength Metallic Materials” (ASTM Special Technical Publication No. 410, 1966) p. 11.Google Scholar
  14. 14.
    M. G. Wyzgoski andG. E. Novak,J. Mater. Sci. 22 (1987) 1715.Google Scholar

Copyright information

© Chupmuoood Hall Ltd 1987

Authors and Affiliations

  • Michael G. Wyzgoski
    • 1
  • Glen E. Novak
    • 1
  1. 1.Polymers DepartmentGeneral Motors Research LaboratoriesWarrenUSA

Personalised recommendations