Real-Space in Situ Study of the II-I Phase transition of Isotactic Poly(1-butene)

被引:27
作者
Xin, Rui [2 ]
Wang, Shaojuan [2 ]
Guo, Zhixin [1 ]
Li, Yunpeng [1 ]
Hu, Jian [2 ]
Sun, Xiaoli [1 ]
Xue, Meiling [2 ]
Zhang, Jie [1 ]
Yan, Shouke [1 ,2 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Qingdao Univ Sci & Technol, Key Lab Rubber Plast, Minist Educ, Qingdao 266042, Peoples R China
基金
中国国家自然科学基金;
关键词
FORM-I; EPITAXIAL CRYSTALLIZATION; POLYMORPHIC TRANSITION; INTERCRYSTALLINE LINKS; SELF-NUCLEATION; CRYSTAL-GROWTH; MELT; POLYBUTENE-1; TRANSFORMATION; KINETICS;
D O I
10.1021/acs.macromol.0c00414
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A new technique has been developed for in situ study of the form II to I phase conversion of isotactic poly(1-butene) (iPBu) in real space. It can distinguish the nucleation and crystal growth processes unequivocally, especially in the early nucleation stage, which can hardly be followed by other traditionally used techniques owing to the limited amount of the transformed form I crystals. Moreover, the subsequent growth process of the form I crystals revealed by the time-dependent images taken during the transition process makes it possible to estimate the growth rate of the form I iPBu crystals during phase transition of ca. 1.65 nm/min at room temperature, which is about 500 times slower than the melt crystallization process. It has also revealed the slow-down crystal growth in the late transformation stage. All of these indicate that the technique is powerful in studying many aspects related to the II-I phase transition of iPBu.
引用
收藏
页码:3090 / 3096
页数:7
相关论文
共 36 条
[1]  
Armeniades C.D., 1967, Journal of Macromolecular Science, Part B: Physics, V1, P309
[2]   Electric-Field-Mediated Reversible Transformation between Supramolecular Networks and Covalent Organic Frameworks [J].
Cai, Zhen-Feng ;
Zhan, Gaolei ;
Daukiya, Lakshya ;
Eyley, Samuel ;
Thielemans, Wim ;
Severin, Kay ;
De Feyter, Steven .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2019, 141 (29) :11404-11408
[3]   Kinetics of the Polymorphic Transition in Isotactic Poly(1-butene) under Uniaxial Extension. New Insights From Designed Mechanical histories. [J].
Cavallo, Dario ;
Kanters, Marc J. W. ;
Caelers, Harm J. M. ;
Portale, Giuseppe ;
Govaert, Leon E. .
MACROMOLECULES, 2014, 47 (09) :3033-3040
[4]   Kinetics of Cross-Nucleation in Isotactic Poly(1-butene) [J].
Cavallo, Dario ;
Gardella, Lorenza ;
Portale, Giuseppe ;
Mueller, Alejandro J. ;
Alfonso, Giovanni C. .
MACROMOLECULES, 2014, 47 (02) :870-873
[5]   Self-nucleation of isotactic poly(1-butene) in the trigonal modification [J].
Cavallo, Dario ;
Gardella, Lorenza ;
Portale, Giuseppe ;
Mueller, Alejandro J. ;
Alfonso, Giovanni C. .
POLYMER, 2014, 55 (01) :137-142
[6]   Metalloorganic Polymerization Catalysis as a Tool To Probe Crystallization Properties of Polymers: The Case of Isotactic Poly (1-butene) [J].
De Rosa, Claudio ;
Auriemma, Finizia ;
Resconi, Luigi .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (52) :9871-9874
[7]   Crystallization Properties and Polymorphic Behavior of Isotactic Poly(1-Butene) from Metallocene Catalysts: The Crystallization of Form I from the Melt [J].
De Rosa, Claudio ;
Auriemma, Finizia ;
de Ballesteros, Odda Ruiz ;
Esposito, Fortunata ;
Laguzza, Domenico ;
Di Girolamo, Rocco ;
Resconi, Luigi .
MACROMOLECULES, 2009, 42 (21) :8286-8297
[8]   The irreversible Form II to Form I transformation in random butene-1/ethylene copolymers [J].
Di Lorenzo, Maria Laura ;
Androsch, Rene ;
Righetti, Maria Cristina .
EUROPEAN POLYMER JOURNAL, 2015, 67 :264-273
[9]   ON THE MOLECULAR MECHANISM OF THE CRYSTAL TRANSFORMATION (TETRAGONAL-HEXAGONAL) IN POLYBUTENE-1 [J].
GOHIL, RM ;
MILES, MJ ;
PETERMANN, J .
JOURNAL OF MACROMOLECULAR SCIENCE-PHYSICS, 1982, B21 (02) :189-201
[10]   Direct High-Temperature Form I Crystallization of Isotactic Poly(1-butene) Assisted by Oriented Isotactic Polypropylene [J].
Guo, Zhixin ;
Xin, Rui ;
Hu, Jian ;
Li, Yunpeng ;
Sun, Xiaoli ;
Yan, Shouke .
MACROMOLECULES, 2019, 52 (24) :9657-9664