English

• 
  
• 1. [1]

     Sheth, J. P.; Xu, J. N.; Wilkes, G. L. Solid state structure-property behavior of semicrystalline poly (ether-block-amide) PEBAX^® thermoplastic elastomers. Polymer 2003, 44, 743-756. doi: 10.1016/S0032-3861(02)00798-X

  2. [2]

     Hepburn, C. Polyurethane elastomers. Springer Science & Business Media, 2012.

  3. [3]

     Oertel, G. Polyurethane handbook. Reinf. Plast 1986, 30, 51.

  4. [4]

     Harrell, L. L. Segmented Polyurethans. Properties as a function of segment size and distribution. Macromolecules 1969, 2, 607-612. doi: 10.1021/ma60012a008

  5. [5]

     Oguro, K.; Kun, N.; Nishimura, H.; Kobayashi, M.; Doi, T. Modified PTMG based thermoplastic polyurethane elastomers. J. Elastom. Plast. 1985, 17, 261-272. doi: 10.1177/009524438501700404

  6. [6]

     Fang, H.; Wang, H.; Sun, J.; Wei, H.; Ding, Y. Tailoring elastomeric properties of waterborne polyurethane by incorporation of polymethyl methacrylate with nanostructural heterogeneity. RSC Adv. 2016, 6, 13589-13599. doi: 10.1039/C5RA26664E

  7. [7]

     Nozaki, S.; Hirai, T.; Higaki, Y.; Yoshinaga, K.; Kojio, K.; Takahara, A. Effect of chain architecture of polyol with secondary hydroxyl group on aggregation structure and mechanical properties of polyurethane elastomer. Polymer 2017, 116, 423-428. doi: 10.1016/j.polymer.2017.03.031

  8. [8]

     Petrović, Z. S.; Ferguson, J. Polyurethane elastomers. Prog. Polym. Sci 1991, 16, 695-836. doi: 10.1016/0079-6700(91)90011-9

  9. [9]

     Prisacariu, C.; Scortanu, E.; Coseri, S.; Agapie, B. Effect of soft segment polydispersity on the elasticity of polyurethane elastomers. Ind. Eng. Chem. Res. 2013, 56, 2316-2322.

  10. [10]

      Tang, D.; Macosko, C. W.; Hillmyer, M. A. Thermoplastic polyurethane elastomers from bio-based poly (δ-decalactone) diols. Polym. Chem. 2014, 5, 3231-3237. doi: 10.1039/C3PY01120H

  11. [11]

      Xiang, D.; Liu, L.; Liang, Y. Effect of hard segment content on structure, dielectric and mechanical properties of hydroxyl-terminated butadiene-acrylonitrile copolymer-based polyurethane elastomers. Polymer 2017, 132, 180-187. doi: 10.1016/j.polymer.2017.11.001

  12. [12]

      Lempesis, N.; In, t. V., Pieter J; Rutledge, G. C. Atomistic simulation of the structure and mechanics of a semicrystalline polyether. Macromolecules 2016, 49, 5714-5726. doi: 10.1021/acs.macromol.6b00555

  13. [13]

      Szycher, M.; Poirier, V. L.; Dempsey, D. J. Development of an aliphatic biomedical-grade polyurethane elastomer. J. Elastom. Plast. 1983, 15, 81-95. doi: 10.1177/009524438301500205

  14. [14]

      Cheng, G.; Liu, X.; Ruixiang, X. U.; Zhang, J.; Fang, S.; Jiang, Z. Effect of polyether soft segments on the properties of hmdi based transparent polyurethane elastomers. Polyurethane Industry 2016, 31, 40-43.

  15. [15]

      Solíscorrea, R. E.; Vargascoronado, R.; Aguilarvega, M.; Cauichrodríguez, J. V.; Román, J. S.; Marcos, A. Synthesis of HMDI-based segmented polyurethanes and their use in the manufacture of elastomeric composites for cardiovascular applications. J. Biomat. Sci-Polym. E 2007, 18, 561-578. doi: 10.1163/156856207780852488

  16. [16]

      Li, Z.; Tan, B. H.; Lin, T.; He, C. Recent advances in stereocomplexation of enantiomeric PLA-based copolymers and applications. Prog. Polym. Sci. 2016, 62, 22-72. doi: 10.1016/j.progpolymsci.2016.05.003

  17. [17]

      Li, Z.; Yuan, D.; Jin, G.; Tan, B. H.; He, C. Facile layer-by-layer self-assembly toward enantiomeric poly (lactide) stereocomplex coated magnetite nanocarrier for highly tunable drug deliveries. ACS Appl. Mater. Interfaces 2016, 8, 1842-1853. doi: 10.1021/acsami.5b09822

  18. [18]

      Tan, B. H.; Muiruri, J. K.; Li, Z.; He, C. Recent progress in using stereocomplexation for enhancement of thermal and mechanical property of polylactide. ACS Sustain. Chem. Eng. 2016, 4, 5370-5391. doi: 10.1021/acssuschemeng.6b01713

  19. [19]

      Huang, J.; Lisowski, M. S.; Runt, J.; Hall, E. S.; Kean, R. T.; Buehler, N.; Lin, J. S. Crystallization and microstructure of poly (L-lactide-co-meso-lactide) copolymers. Macromolecules 1998, 31, 2593-2599. doi: 10.1021/ma9714629

  20. [20]

      Lv, R.; Peng, N.; Jin, T.; Na, B.; Wang, J.; Liu, H. Stereocomplex mesophase and its phase transition in enantiomeric polylactides. Polymer 2017, 116, 324-330. doi: 10.1016/j.polymer.2017.04.004

  21. [21]

      Abayasinghe, N. K.; Perera, K. P.; Thomas, C.; Daly, A.; Suresh, S.; Burg, K.; Harrison, G. M.; Jr, S. D. Amido-modified polylactide for potential tissue engineering applications. J. Biomat. Sci. Polym. E 2004, 15, 595-606. doi: 10.1163/156856204323046861

  22. [22]

      Panyam, J.; Vinod Labhasetwar, V. Sustained cytoplasmic delivery of drugs with intracellular receptors using biodegradable nanoparticles. Mol. Pharm. 2004, 1, 77-84. doi: 10.1021/mp034002c

  23. [23]

      Jain, R. A. The manufacturing techniques of various drug loaded biodegradable poly (lactide-co-glycolide) (PLGA) devices. Biomaterials 2000, 21, 2475-2490. doi: 10.1016/S0142-9612(00)00115-0

  24. [24]

      Jung, T.; Kamm, W.; Breitenbach, A.; Kaiserling, E.; Xiao, J. X.; Kissel, T. Biodegradable nanoparticles for oral delivery of peptides: is there a role for polymers to affect mucosal uptake? Eur. J. Pharm. Biopharm. 2000, 50, 147-160. doi: 10.1016/S0939-6411(00)00084-9

  25. [25]

      Gu, S. Y.; Yang, M.; Yu, T.; Ren, T. B.; Ren, J. Synthesis and characterization of biodegradable lactic acid-based polymers by chain extension. Polym. Inter. 2008, 57, 982-986. doi: 10.1002/pi.v57:8

  26. [26]

      Hoshi, M.; Ieshige, M.; Saitoh, T.; Nakagawa, T. Separation of aqueous phenol through polyurethane membranes by pervaporation. II. Influence of diisocyanate and diol compounds and crosslinker. J. Appl. Polym. Sci. 1999, 71, 439-448. doi: 10.1002/(ISSN)1097-4628

  27. [27]

      Hiltunen, K.; Härkönen, M.; Seppälä, J. V.; Väänänen, T. Synthesis and characterization of lactic acid based telechelic prepolymers. Macromolecules 1996, 29, 8677-8682. doi: 10.1021/ma960402k

  28. [28]

      Schneider, N. S.; Matton, R. W. Thermal transition behavior of polybutadiene containing polyurethanes. Polym. Eng. Sci. 1979, 19, 1122-1128. doi: 10.1002/(ISSN)1548-2634

  29. [29]

      Xu, M.; Macknight, W. J.; Chen, C. H. Y.; Thomas, E. L. Structure and morphology of segmented polyurethanes: 1. Influence of incompatability on hard-segment sequence length. Polymer 1983, 24, 1327-1332. doi: 10.1016/0032-3861(83)90068-X

  30. [30]

      Hesketh, T. R.; Vanbogart, J. W. C.; Cooper, S. L. Differential scanning calorimetry analysis of morphological-changes in segmented elastomers. Polym. Eng. Sci. 1980, 20, 190-197. doi: 10.1002/(ISSN)1548-2634

  31. [31]

      Tsuji, H.; Ishida, T. Poly (L-lactide). X. Enhanced surface hydrophilicity and chain-scission mechanisms of poly (L-lactide) film in enzymatic, alkaline, and phosphate-buffered solutions. J. Appl. Polym. Sci. 2003, 87, 1628-1633. doi: 10.1002/app.11605

  32. [32]

      Lucas, J. C.; Failla, M. D.; Smith, F. L.; Mandelkern, L. The double yield in the tensile deformation of the polyethylenes. Polym. Eng. Sci. 1995, 35, 1117-1123. doi: 10.1002/(ISSN)1548-2634

  33. [33]

      Popli, R.; Mandelkern, L. Influence of structural and morphological factors on the mechanical-properties of the polyethylenes. J. Polym. Sci. Part. B: Polym. Phys. 1987, 25, 441-483. doi: 10.1002/polb.1987.090250301

  34. [34]

      Lendlein, A.; Kelch, S. Shape-memory polymers. Encyclopedia of Materials Science & Technology 2002, 41, 2034-2057.

  35. [35]

      Zhang, L.; Jiang, Y.; Xiong, Z.; Liu, X.; Na, H.; Zhang, R.; Zhu, J. Highly recoverable rosin-based shape memory polyurethanes. J. Mater. Chem. A 2013, 1, 3263-3267. doi: 10.1039/c3ta01655b

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