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Warianty tytułu
Konferencja
Sol-Gel Materials Research, Technology, Applications SGM'04, 6-11 june 2004
Języki publikacji
Abstrakty
Segmented block copolymers were synthesized from hydroxyl terminated liquid natural rubber (HTNR) and polyurethane oligomers (PU), formed from 1,4-butanediol (1,4-BDO) and toluene diisocyanate (TDI). The samples were synthesized in solution in two series by the one-step and two-step methods. They were characterized by spectral analysis, thermal analysis, etching studies, microscopy and mechanical testing. IR and NMR spectral data, along with etching studies, support the notion that a chemical reaction leads to block copolymerization. Differential scanning calorimetric (DSC) analysis showed a soft segment glass transition temperature between -62 °C and -63 °C and a hard segment glass transition temperature between 87 °C and 100 °C for different samples. This observation and two-stage thermal decomposition of the samples in thermogravimetric analysis (TGA) clearly indicate that the block copolymers are completely phase-segregated systems. The amorphous heterophase morphology of the samples is indicated by SEM, which shows well-defined beads of hard phase dispersed in a matrix. SEM results, along with the etching studies, revealed that the samples are systems consisting of block copolymers and some quantity of uncoupled polyurethane homopolymers in the form of beads. The homopolymer beads suggest that the efficiency of the chain extension in the present method of synthesis is slightly lower than expected. Tensile properties improved with the hard segment content in the samples. Low hard segment content leads to a flexible elastomer, while at the high one rigid plastics are formed. Intermediate compositions yielded rigid elastomers. Two-step samples showed slightly better properties compared to the one-step samples. This may be due to the systematic way by which the reaction progresses in two-step synthesis. The overall properties are found to be lower than that of the conventional polyurethane elastomers. This is attributed to the absence of phase mixing and the inability of the soft segments to crystallise under strain due to their short segments.
Słowa kluczowe
Wydawca
Czasopismo
Rocznik
Tom
Strony
227--245
Opis fizyczny
Bibliogr. 14 poz.
Twórcy
autor
- School of Chemical Sciences, Mahatma Gandhi University, Priyadarshini Hills, Kottayam - 686 560, Kerala, India
autor
autor
Bibliografia
- [1] FRANCIS D.J., RAVINDRAN T., NAYAR M.R.G., 32nd Annual Polyurethane Technical Marketing Conference, San Francisco, October 1–4, 1989, 373.
- [2] PAUL C.J., NAIR M.R.G., Ind. J. Nat. Rubber Research, 1&2 (1992), 199.
- [3] PAUL C.J., NAIR M.R.G., NEELAKANTAN N.R., KOSHY P., Polym. Eng. Sci., 3 (1998), 440.
- [4] PAUL C.J., NAIR M.R.G., NEELAKANTAN N.R., KOSHY P., IDAGE B.B., BHELHEKAR A.A., Polymer 26 (1998), 6861.
- [5] RAVINDRAN T., NAYAR M.R.G., FRANCIS D.J., J. Appl. Polym. Sci., 42 (1991), 325.
- [6] RAVINDRAN T., NAYAR M.R.G., FRANCIS D.J., J. Appl. Polym. Sci., 35 (1988), 122.
- [7] GUPTA T., ADHIKARI B., Thermochim. Acta, 402 (2003), 169.
- [8] SATAVA V., Thermochim. Acta, 2 (1971), 423.
- [9] LEE C.Y., KIM J., SUH K.D., J. Appl. Polym. Sci., 78 (2000), 1853.
- [10] GORNA K., POLOWINSKI S., GOGOLEWSKI S., J. Polym. Sci., A, Polym. Chem., 40 (2002), 156.
- [11] PETROVIC Z.S., FERGUSON I. Prog. Polym. Sci. 16 (1991), 695.
- [12] CHANG A.L., BRIBER R.B., THOMAS E.L., ZDRAHALA R.J., CRITCHFIELD F.E., Polymer 23 (1982), 1060.
- [13] SMITH T.L., Polym. Eng. Sci., 17 (1977), 129.
- [14] SPECKHARD T.A., GIBSON P.E., COOPER S.L., CHANG V.S.C., KENNEDY J.P., Polymer 26 (1985), 55.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BPW7-0002-0023