[1] |
PAN P, INOUE Y. Polymorphism and isomorphism in biodegradable polyesters[J]. Prog. Polym. Sci., 2009, 34(7):605-640.
|
[2] |
LIU G M, ZHANG X Q, WANG D J. Tailoring crystallization:towards high-performance poly(lactic acid)[J]. Adv. Mater., 2014, 26(40):6905-6911.
|
[3] |
IKADA Y, JAMSHIDI K, TSUJI H, et al. Stereocomplex formation between enantiomeric poly(lactides)[J]. Macromolecules, 1987, 20(4):904-906.
|
[4] |
PAN P, YANG J, SHAN G, et al. Temperature-variable FTIR and solid-state 13C NMR investigations on crystalline structure and molecular dynamics of polymorphic poly(L-lactide) and poly(L-lactide)/poly(D-lactide) stereocomplex[J]. Macromolecules, 2011, 45(1):189-197.
|
[5] |
YUI N, DIJKSTRA P J, FEIJEN J. Stereo block copolymers of L- and D-lactides[J]. Macromol. Chem., 1990, 191(3):481-488.
|
[6] |
HIRATA M, KIMURA Y. Thermomechanical properties of stereoblock poly(lactic acid)s with different PLLA/PDLA block compositions[J]. Polymer, 2008, 49(11):2656-2661.
|
[7] |
MASUTANI K, LEE C W, KIMURA Y. Synthesis of stereo multiblock polylactides by dual terminal couplings of poly-L-lactide and poly-D-lactide prepolymers:a new route to high-performance polylactides[J]. Polymer, 2012, 53(26):6053-6062.
|
[8] |
LI L, ZHONG Z, JEU W, et al. Crystal structure and morphology of poly(L-lactide-b-D-lactide) diblock copolymers[J]. Macromolecules, 2004, 37(23):8641-8646.
|
[9] |
HIRATA M, KOBAYASHI K, KIMURA Y. Synthesis and properties of high-molecular-weight stereo di-block polylactides with nonequivalent D/L ratios[J]. J. Polym. Sci., Part A:Polym. Chem., 2010, 48(4):794-801.
|
[10] |
MASUTANI K, KAWABATA S, AOKI T, et al. Efficient formation of stereocomplexes of poly(L-lactide) and poly(D-lactide) by terminal Diels-Alder coupling[J]. Polym. Int., 2010, 59(11):1526-1530.
|
[11] |
TSUJI H, WADA T, SAKAMOTO Y, et al. Stereocomplex crystallization and spherulite growth behavior of poly(L-lactide)-bpoly(D-lactide) stereodiblock copolymers[J]. Polymer, 2010, 51(21):4937-4947.
|
[12] |
TSUJI H, HYON S H, IKADA Y. Stereocomplex formation between enantiomeric poly(lactic acid)s(3):Calorimetric studies on blend films cast from dilute solution[J]. Macromolecules, 1991, 24(20):5651-5656.
|
[13] |
TSUJI H, IKADA Y. Stereocomplex formation between enantiomeric poly(lactic acid)s (9):Stereocomplexation from the melt[J]. Macromolecules, 1993, 26(25):6918-6926.
|
[14] |
PAN P J, HAN L L, BAO J N, et al. Competitive stereocomplexation, homocrystallization, and polymorphic crystalline transition in poly(L-lactic acid)/poly(D-lactic acid) racemic blends:molecular weight effects[J]. J. Phys. Chem. B, 2015, 119(21):6462-6470.
|
[15] |
TSUJI H, IKADA Y. Stereocomplex formation between enantiomeric poly(lactic acid)s(6):Binary blends from copolymers[J]. Macromolecules, 1993, 25(21):5719-5723.
|
[16] |
LIU Y, SUN J, BIAN X, et al. Melt stereocomplexation from poly(L-lactic acid) and poly(D-lactic acid) with different optical purity[J]. Polym. Degrad. Stab., 2013, 98(4):844-852.
|
[17] |
FUKUSHIMA K, HIRATA M, KIMURA Y. Synthesis and characterization of stereoblock poly(lactic acid)s with nonequivalent D/L sequence ratios[J]. Macromolecules, 2007, 40(9):3049-3055.
|
[18] |
MAILLARD D, PRUD'HOMME R E. Difference between crystals obtained in PLLA-rich or PDLA-rich stereocomplex mixtures[J]. Macromolecules, 2010, 43(9):4006-4010.
|
[19] |
ISONO T, KONDO Y, OTSUKA I, et al. Synthesis and stereocomplex formation of star-shaped stereoblock polylactides consisting of poly(L-lactide) and poly(D-lactide) arms[J]. Macromolecules, 2013, 46(21):8509-8518.
|
[20] |
ISONO T, KONDO Y, OZAWA S, et al. Stereoblock-like brush copolymers consisting of poly(L-lactide) and poly(D-lactide) side chains along poly(norbornene) backbone:synthesis, stereocomplex formation, and structure-property relationship[J]. Macromolecules, 2014, 47(20):7118-7128.
|
[21] |
SHAO J, SUN J, BIAN X, et al. Investigation of poly(lactide) stereocomplexes:3-armed poly(L-lactide) blended with linear and 3-armed enantiomers[J]. J. Phys. Chem. B, 2012, 116(33):9983-9991.
|
[22] |
BIELA T, DUDA A, PENCZEK S. Enhanced melt stability of star-shaped stereocomplexes as compared with linear stereocomplexes[J]. Macromolecules, 2006, 39(11):3710-3713.
|
[23] |
TSUJI H, HYON S H, IKADA Y. Stereocomplex formation between enantiomeric poly(lactic acid)s(4):Differential scanning calorimetric studies on precipitates from mixed solutions of poly(D-lactic acid) and poly(L-lactic acid)[J]. Macromolecules, 1991, 24(20):5657-5662.
|
[24] |
FURUHASHI Y, YOSHIE N. Stereocomplexation of solvent-cast poly (lactic acid) by addition of non-solvents[J]. Polym. Int., 2012, 61(2):301-306.
|
[25] |
TSUJI H, YAMAMOTO S. Enhanced stereocomplex crystallization of biodegradable enantiomeric poly(lactic acid)s by repeated casting[J]. Macromol. Mater. Eng., 2011, 296(7):583-589.
|
[26] |
SUN J, YU H, ZHUANG X, et al. Crystallization behavior of asymmetric PLLA/PDLA blends[J]. J. Phys. Chem. B, 2011, 115(12):2864-2869.
|
[27] |
HE Y, XU Y, WEI J, et al. Unique crystallization behavior of poly(L-lactide)/poly(D-lactide) stereocomplex depending on initial melt states[J]. Polymer, 2008, 49(26):5670-5675.
|
[28] |
BAO R Y, YANG W, JIANG W R, et al. Polymorphism of racemic poly(L-lactide)/poly(D-lactide) blend:effect of melt and cold crystallization[J]. J. Phys. Chem. B, 2013, 117(13):3667-3674.
|
[29] |
ZHANG J, TASHIRO K, TSUJI H, et al. Investigation of phase transitional behavior of poly(L-lactide)/poly(D-lactide) blend used to prepare the highly-oriented stereocomplex[J]. Macromolecules, 2007, 40(4):1049-1054.
|
[30] |
NA B, ZHU J, LV R, et al. Stereocomplex formation in enantiomeric polylactides by melting recrystallization of homocrystals:crystallization kinetics and crystal morphology[J]. Macromolecules, 2014, 47(1):347-352.
|
[31] |
XIONG Z, LIU G, ZHANG X, et al. Temperature dependence of crystalline transition of highly oriented poly(L-lactide)/poly(D-lactide) blend:in-situ synchrotron X-ray scattering study[J]. Polymer, 2013, 54(2):964-971.
|
[32] |
DUAN Y, LIU J, SATO H, et al. Molecular weight dependence of the poly(L-lactide)/poly(D-lactide) stereocomplex at the air-water interface[J]. Biomacromolecules, 2006, 7(10):2728-2735.
|
[33] |
CHANG L, WOO E M. Effects of molten poly(3-hydroxybutyrate) on crystalline morphology in stereocomplex of poly(L-lactic acid) with poly(D-lactic acid)[J]. Polymer, 2011, 52(1):68-76.
|
[34] |
BAO R, YANG W, WEI X, et al. Enhanced formation of stereocomplex crystallites of high molecular weight poly(L-lactide)/poly(D-lactide) blends from melt by using poly(ethylene glycol)[J]. ACS Sustainable Chem. Eng., 2014, 2(10):2301-2309.
|
[35] |
FUKUSHIMA K, CHANG Y H, KIMURA Y. Enhanced stereocomplex formation of poly(L-lactic acid) and poly(D-lactic acid) in the presence of stereoblock poly(lactic acid)[J]. Macromol. Biosci., 2007, 7(6):829-835.
|
[36] |
URAYAMA H, KANAMORI T, FUKUSHIMA K. Controlled crystal nucleation in the melt-crystallization of poly(L-lactide) and poly(L-lactide)/poly(D-lactide) stereocomplex[J]. Polymer, 2003, 44(19):5635-5641.
|
[37] |
OUCHI M, OKAMOTO H, NAKANO M. Polylactic acid resin and composition and molded article of the same:US0097074[P]. 2008-04-24.
|
[38] |
HAN L, PAN P, SHAN G, et al. Stereocomplex crystallization of high-molecular-weight poly(L-lactic acid)/poly(D-lactic acid) racemic blends promoted by a selective nucleator[J]. Polymer, 2015, 63(10):144-153.
|
[39] |
BAI H, LIU H, BAI D, et al. Enhancing the melt stability of polylactide stereocomplexes using a solid-state cross-linking strategy during a melt-blending process[J]. Polym. Chem., 2014, 5(20):5985-5993.
|