Mechanical properties and fractography of block copolymers based on NR and MDI-based polyurethanes
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Abstract
Five series of block copolymers were synthesized from hydroxyl-terminated liquid natural rubber (HTNR) and polyurethane (PU) oligomers, from various diols and diphenyl methane-4,4′-diisocyanate (MDI). They were characterized by mechanical testing and fracture studies (SEM analysis). The block copolymer characteristics were assessed on the basis of the composition and the type of extender diols. Mechanical properties were found to be strongly dependent on the copolymer composition in all the series. Tensile properties were found to improve with the hard segment content. At low hard segment content samples resemble flexible elastomers whereas at high hard segment content they behave as rigid plastics. Where bisphenol A (BPA) is used as the extender diol sample rigidity was higher compared to the samples with aliphatic diols which is attributed to the presence of aromatic ring system in the former samples. Fracture mechanism was found to vary from ductile fracture to rigid and brittle fracture as the hard segment content increased. Fractography also shows the presence of some beads disposed on the sample surface which could be the uncombined polyurethane homopolymer fractions.
Keywords
Natural rubber Polyurethanes Block copolymers Fractography Mechanical properties SEM Phase segregationReferences
- 1.Van Bogart JWC, Gibson PE, Cooper SL (1983) J Polym Sci Polym Phys Ed 21:65CrossRefGoogle Scholar
- 2.Chu B, Gao T, Li Y, Wang J, Desper CR, Byre CA (1992) Macromolecules 25:5724CrossRefGoogle Scholar
- 3.Chee KK, Farris RJ (1984) J Appl Polym Sci 29:2529CrossRefGoogle Scholar
- 4.Younes H, Cohn DJ (2004) Biomed Mater Res 29:1301Google Scholar
- 5.Smith TL (2004) Polym Eng Sci 17:129CrossRefGoogle Scholar
- 6.Hesketh TR, Van Bogart JWC (1980) Polym Eng Sci 20:190CrossRefGoogle Scholar
- 7.Paik Sung CS, Schneider NS (1975) Macromolecules 8:68CrossRefGoogle Scholar
- 8.Lee DK, Tsai HB (2000) J Appl Polym Sci 75:167CrossRefGoogle Scholar
- 9.Ciobanu C, Han X, Cascaval C, Guo F, Rosu D, Ignat LJ (2003) Appl Polym Sci 87:1858CrossRefGoogle Scholar
- 10.Speckhard TA, Gibson PE, Cooper SL, Chang VSC, Kennedy JP (1985) Polymer 26:55CrossRefGoogle Scholar
- 11.Xe M, MacKnight WJ, Chen CHY, Thomas EL (1983) Polymer 24:1327CrossRefGoogle Scholar
- 12.Yoon SC, Ratner BD, Ivan B, Kennedy JP (1994) Macromolecules 27:1548CrossRefGoogle Scholar
- 13.Cawse JL, Stanford JL, Still RH (1986) J Appl Polym Sci 36:1549CrossRefGoogle Scholar
- 14.Paul CJ, Nair MRG, Neelakantan NR, Koshy P, Idage BB, Bhelhekar AA (1998) Polymer 39:6861CrossRefGoogle Scholar
- 15.Paul CJ, Nair MRG, Koshy P, Idage BB (1999) J Appl Polym Sci 74:706CrossRefGoogle Scholar
- 16.Paul CJ, Nair MRG, Neelakantan NR, Koshy P (1998) Polym Eng Sci 38:440CrossRefGoogle Scholar
- 17.Gopakumar S, Paul CJ, Nair MRG (2005) J Mat Sci Poland 23:227Google Scholar
- 18.Radhakrishnan Nair MN, Gopinathan Nair MRJ (2008) Mat Sci 43:738CrossRefGoogle Scholar
- 19.Ravindran T, Nair MRG, Francis DJ (1988) J Appl Polym Sci 35:1227CrossRefGoogle Scholar
- 20.Sukumar P, Jayashree V, Gopinathan Nair MR, Radhakrishnan Nair MN (2009) J Appl Polym Sci 111:19CrossRefGoogle Scholar