Krystalizace a transformace polybutenu-1

Kaszonyiová, Martina; Rybnikář, František; Geil, Phillip H.

dc.title	Krystalizace a transformace polybutenu-1	cs
dc.title	Crystalization and transformation of polybutene-1	en
dc.contributor.author	Kaszonyiová, Martina
dc.contributor.author	Rybnikář, František
dc.contributor.author	Geil, Phillip H.
dc.relation.ispartof	Journal of Macromolecular Science, Part B: Physics
dc.identifier.issn	0022-2348 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued	2004
utb.relation.volume	43
utb.relation.issue	5
dc.citation.spage	1095
dc.citation.epage	1114
dc.type	article
dc.language.iso	en
dc.publisher	Taylor & Francis Inc.	en
dc.identifier.doi	10.1081/MB-200033322
dc.relation.uri	https://www.tandfonline.com/doi/full/10.1081/MB-200033322
dc.relation.uri	https://www.tandfonline.com/doi/pdf/10.1081/MB-200033322
dc.subject	Isotermální krystalizace	cs
dc.subject	rtg- diffrakce	cs
dc.subject	Isoterrmal crystalization	en
dc.subject	sodium salicilate	en
dc.subject	talc	en
dc.subject	X-ray diffraction	en
dc.description.abstract	Isotermní krystalizace a fázová II- I transformace za různých teplot byla zkoumána RTG difrakcí. Krystalizační rychlost může být zvýšenáa přidáním různých pevných látek jako salicilan sodný a mastek, kterí např. zvyšují rychlost víc než 100% a nebo snižují víc než 300%.	cs
dc.description.abstract	The isothermal crystallization and phase II # I transformation of bulk polybutene-1 at various temperatures has been characterized by X-ray diffraction. The crystallization rate can be increased or decreased by the addition of various solids, with sodium salicylate and talc, e.g., increasing the rate by >100% and decreasing the rate by >300%, respectively. The nucleating agents have no effect on the transformation rate, which is, however, increased slightly in the presence of water and ethanol and significantly in the presence of liquids which are solvents at elevated temperatures or by the application of tension, compression or temperature cycling. The transformation rate of non-treated polymer is greatest near 25 °C, decreasing at higher and lower temperatures.	en
utb.faculty	Faculty of Technology
dc.identifier.uri	http://hdl.handle.net/10563/1000357
utb.identifier.rivid	RIV/70883521:28110/04:63502540
utb.identifier.obdid	12052808
utb.identifier.scopus	2-s2.0-5744250325
utb.identifier.wok	000224162700015
utb.source	j-riv
utb.contributor.internalauthor	Kaszonyiová, Martina
utb.contributor.internalauthor	Rybnikář, František
utb.fulltext.affiliation	M. Kaszonyiova,1 F. Rybnikar,1,* and P. H. Geil1,2 1 Department of Polymer Material and Technology, University of Thomas Bata, Zlin, Czech Republic 2 Department of Materials Science and Engineering, University of Illinois, Urbana, Illinois, USA *Correspondence: F. Rybnikar, Department of Polymer Material and Technology, University of Thomas Bata, Zlin 76001, Czech Republic; E-mail: rybnikar@ft.utb.cz
utb.fulltext.dates	Received May 2, 2003 Accepted April 28, 2003
utb.fulltext.references	1. Geil, P.H. Polymer Single Crystals; Interscience: New York, 1963, 427. 2. Turner-Jones, A. J. Polym. Sci. Part B 1963, 1, 455. 3. Natta, G.; Corradini, P.; Bassi, I.W. Makromol. Chem. 1957, 21, 240. 4. Holland, V.F.; Miller, R.L. J. Appl. Phys. 1964, 35, 3241. 5. Goldbach, G.; Peitscher, G. J. Polym. Sci. 1986, B6, 783. 6. Armeniades, C.D.; Baer, E. J. Macromol. Sci. Phys. 1967, B1, 309. 7. Kopp, S.; Whitmann, J.C.; Lotz, B. Polymer 1994, 35, 908. 8. Kopp, S.; Whitmann, J.C.; Lotz, B. Polymer 1994, 35, 916. 9. Zannetti, R.; Manarersi, P.; Buzzoni, G.C. Chim. Ind. 1961, 43, 735. 10. Danuso, F.; Gianotti, G. Makromol. Chem. 1963, 61, 139. 11. Cojazzi, G.; Malta, V.; Cellotti, G.; Zanneti, R. Makromol. Chem. 1976, 177, 915. 12. Chau, K.W.; Yang, Y.C.; Geil, P.H. J. Mater. Sci. 1986, 21, 3002. 13. Icenogle, R.D. J. Polym. Sci. 1985, 23, 1369. 14. Hsu, T.C.; Geil, P.H. J. Macromol. Sci. Phys. 1989, B28, 69. 15. Fujiwara, Y. Polym. Bull. 1985, 13, 253. 16. Kopp, S.; Wittmann, J.C.; Lotz, B. J. Mater. Sci. 1994, 29, 6159. 17. Chau, K.W.; Geil, P.H. J. Macromol. Sci. Phys. 1984, B23, 115. 18. Rybnikar, F. J. Appl. Polym. Sci. 1985, 30, 1949. 19. Kaszonyiova, M.; Rybnikar, F. (to be published). 20. Carr, S.H.; Keller, A.; Baer, E. J. Polym. Sci. A-2 1970, 4, 1467. 21. Morgan, L.B. Phil. Trans. Royal Soc. (Lond.) 1954, A297, 13. 22. Hsu, C.C.; Geil, P.H. J. Macromol. Sci. Phys. 1986, B25, 433. 23. Oda, T.; Maeda, M.; Hibi, S.; Watanabe, S. Kobunshi Ronbushu, Eng. Ed. 1974, 3, 189. 24. Weynant, E.; Haudin, J.C.; Sell, C.G. J. Mater. Sci. 1982, 17, 1017. 25. Petraccone, V.; Pirozzi, B.; Frasca, A.; Corradini, P. Eur. Polym. J. 1976, 12, 323. 26. Tadokoro, H. Structure of Crystalline Polymers; Wiley-Interscience: New York, 1976; 356. 27. Hsu, T.C.; Geil, P.H. Polym. Commun. 1990, 31, 105.
utb.fulltext.sponsorship	This research was supported, in part, by Grant ME-131 from the Granting Agency of the Czech Republic and Grant DMR 0234678 from the Polymer and International Programs sections of the US, National Science Foundation. Appreciation is expressed to Prof. B. Lotz, University of Strasbourg, for numerous helpful comments.
utb.fulltext.projects	GACR ME-131
utb.fulltext.projects	DMR 0234678
utb.fulltext.faculty	Faculty of Technology
utb.fulltext.ou	Department of Polymer Material and Technology