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Emission of organic compounds from two types of polytrioxane (colorless and black-smoke pigmented) has been measured by using a 20-cm3 chamber connected directly to a gas chromatograph. Measurements were performed at 40, 60, and 80 C degrees at a flow rate of 0.45 cm3 min-1. High surface to volume ratio and a relatively large sample loop (3 cm3) enabled detection of signals from organic substances present at low concentrations (~μg cm-3). The results obtained revealed that for the pigmented polytri-oxane the rate of emission of organic compounds and the rate constants for the process were higher than for the colorless form. In contrast, the ac-tivation energy was slightly higher for emission of trioxane from the pig-mented material. For trioxepane emission activation energies were similar. Results show the pigment had no retardant activity on emission of organic compounds from the polymer. The activation energies determined for emis-sion of organic compounds were in the range 15 to 60 kJ mol-1. The rate constants (from 7.6 × 10-10 to 9.2 × 10-8 cm-2 s-1) suggest diffusion or de-sorption are occurring within the polymer matrix.
Słowa kluczowe
Czasopismo
Rocznik
Tom
Strony
37--48
Opis fizyczny
Bibliogr. 22 poz., rys., tab.
Twórcy
autor
- Department of Chemistry, Jagiellonian University, ul. Gronostajowa 3, 30-387 Kraków, Poland
autor
- Department of Environmental Physics, Faculty of Physics and Nuclear Techniques, AGH–University of Science and Technology, al. Mickiewicza 30, 30-059 Kraków, Poland
autor
- Department of Chemistry, Jagiellonian University, ul. Gronostajowa 3, 30-387 Kraków, Poland
Bibliografia
- [1] Ch. Yu and D. Crump, Build. Environ., 33, 357 (1998)
- [2] F. Haghighat and L. de Bellis, Build. Environ., 33, 261 (1998)
- [3] P. Wolkoff, Atmos. Environ., 32, 2659 (1998)
- [4] P. Wolkoff, Sci. Total Environ., 227, 197 (1999)
- [5] S. Soundararajan and S.C. Shit, Polym. Test., 20, 313 (2001)
- [6] M.S. Bhatnagar, Polyacetals – Part 1, Popular Plastics and Packaging, 46, 77 (2001)
- [7] G. Sextro, Industrial Polymers Handbook, Vol. 2, Wiley–VCH, Weinheim, 2001, 979–1000
- [8] S.H. Teoh, Int. J. Fatigue, 22, 825 (2000)
- [9] N. Yamasaki, H. Nagahara, and J. Masamoto, Tetrahedron Lett., 42, 271 (2001)
- [10] W. Kern and H. Cherdron, Makromol. Chem, 40, 101 (1960)
- [11] W. Kern, H. Cherdron, V. Jaaks, U. Baader, H. Debig, A. Giefer, and L. Hohr, Angew. Chem., 73, 177 (1961)
- [12] W. Kern, H. Cherdron, and L. Hohr, Macromol. Chem., 42, 271 (2001)
- [13] S. Torikai, J. Polym. Sci. A-2, 239, 3461 (1963)
- [14] L.A. Dudina, L.V. Karmilova, E.N. Tryapitsyna, and N.S. Erikolpyan, J. Polym. Sci C, 16, 2277 (1967)
- [15] G.M. Murach, M. Adamowska, and S. Talik, Prace Naukowe Instytutu Podstaw Elektrotechniki i Elektrotechnologii Politechniki Wrocławskiej, 34, 169 (1998)
- [16] D. Capandis, Tribologia, 33, 80 (2001)
- [17] H. Li, X. Qi, G. Zhang, L. Wei, X. Wang, and X. Zhang, Gongcheng Suliao Yingyong, 30, 40 (2002)
- [18] V.M. Archoudoulaki and S. Seidler, Proc. Conf. Advances in Mechanical Behavior, Plasticity and Damage, Tours, France, Nov. 7–9, 2000, Elsevier, Oxford, 2000, 1, 261–266
- [19] S. Tsuge and H. Ohtani, Pol. Deg. Stab., 58, 109 (1997)
- [20] M. Day, J. D. Cooney, C. Touchette-Barrette, and S.E. Sheehan, J. Anal. Appl. Pyr., 52, 199 (1999)
- [21] M.H. Klopffer and B. Flaconneche, Oil & Gas Science and Technology – Review IFP, 56, 223 (2001)
- [22] J.J. Ritter and N.K. Adams, Anal. Chem., 48, 612 (1976)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BAT3-0028-0048