Abstract
A new method for evaluating biodegradability of starch-based and certain other polymer blends uses the pre- and postexposure stable carbon isotope composition of material coupled with weight loss data to determine which components have degraded. The naturally occurring stable isotope of carbon.13C, is enriched in corn starch (δ13C, approx. −11‰) compared to petroleum-derived synthetic polymers (δ13C, approx. −32‰). Results on starch-synthetic polymer blends indicate that the δ13C signatures of these blends are near-linear mixtures of their component δ13C. Values of a δ13C for starch-synthetic polymer blends exposed to biologically active laboratory soil and artificial seawater conditions are depleted in13C compared to unexposed samples, suggesting loss of the starch component. Combined with weight loss data for the exposed samples, the δ13C values are statistically consistent with models requiring loss of the soluble component glycerin, followed by loss of starch, then petrochemical polymer, or simultaneous loss of starch and petrochemical polymer. Replicate δ13C analyses of starch-synthetic polymer blends increase the statistical power of this relatively inexpensive, accessible technique to discriminate between degrading components.
Similar content being viewed by others
References
B. Smith, personal communication, Novon Division of Warner-Lambert Industries.
M. L. Sykes, I. F. West, R. W. Gauldie, and C. E. Thacker (1994) submitted for publication.
H. C. Urey, H. A. Lowenstam, S. Epstein, and C. R. McKinney (1951)Bull. Geol. Soc. Am. 62, 399–416.
E. T. Degens (1969) in G. Eglinton and M. T. J. Murphy (Eds.),Organic Geochemistry: Methods and Results, Springer-Verlag, New York, pp. 304–329.
C. Junge, M. Schidlowski, R. Eichmann, and H. Pietrek (1975)J. Geophys. Res. 80, 4542–4552.
J. Hoefs (1980)Stable Isotope Geochemistry, 2nd ed., Springer-Verlag, New York.
G. Faure (1986)Principles of Isotope Geology, John Wiley and Sons, New York, pp. 491–512.
R. Park and S. Epstein (1960)Geochim. Cosmochim. Acta 21, 110–126.
T. Whelan, W. M. Sackett, and C. R. Benedict (1973)Plant Physiol. 51, 1051–1054.
K. D. Monson, and J. M. Hayes (1982)Geochim. Cosmochim. Acta 46, 139–149.
W. J. Stahl (1979) in E. Jager and J. C. Hunziker (Eds.),Lectures in Isotope Geology, Springer Verlag, Berlin, pp. 274–282.
H.-W. Yeh and S. Epstein (1981)Geochem. Cosmochim. Acta 45, 753–762.
C. Craig (1953)Geochim. Cosmochim. Acta 3, 53–92.
C. Craig (1957)Geochim. Cosmochim. Acta 12, 133–149.
C. R. McKinney, J. M. McCrea, S. Epstein, H. A. Allen, and H. C. Urey (1950)Rev. Sci. Inst. 1, 724–730.
J. M. McCassieet al. (1994) submitted for publication.
M. L. Sykes, I. F. West, C. E. Thacker, and R. W. Gauldie (1994)J. Environ. Polym. Degrad. Submitted for publication.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Sykes, M.L., Yeh, HW., West, I.F. et al. A carbon-13 method for evaluating degradation of starch-based polymers. J Environ Polym Degr 2, 201–209 (1994). https://doi.org/10.1007/BF02067446
Issue Date:
DOI: https://doi.org/10.1007/BF02067446