聚(乙烯基对苯二甲酸二烷基酯)的非寻常相转变

刘鑫; 郑晓慧; 刘小青; 赵瑞颖; 赵体鹏; 刘琛阳; 孙平川; 陈尔强

doi:10.11777/j.issn1000-3304.2017.17082

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聚(乙烯基对苯二甲酸二烷基酯)的非寻常相转变

研究论文 | 更新时间：2021-01-27

- 聚(乙烯基对苯二甲酸二烷基酯)的非寻常相转变
- Unusual Phase Transition of Poly(di(alkyl) vinylterephthalates)
- 高分子学报 2017年第9期页码：1506-1516
- 作者机构：
  
  1.北京大学化学与分子工程学院高分子化学与物理教育部重点实验室北京 100871
  2.中国科学院化学研究所中国科学院工程塑料重点实验室北京 100190
  3.南开大学化学学院功能高分子材料教育部重点实验室天津 300071
- 作者简介：
  
  刘琛阳, E-mail:liucy@iccas.ac.cnChen-yang Liu, E-mail:liucy@iccas.ac.cn
  陈尔强, E-mail:eqchen@pku.edu.cnEr-qiang Chen, E-mail:eqchen@pku.edu.cn
- 基金信息：
  
  国家自然科学基金(20990232);国家自然科学基金(21634001);国家重点基础研究发展计划（973计划）(2011CB606004)
- DOI：10.11777/j.issn1000-3304.2017.17082
  中图分类号：
- 纸质出版日期：2017-9-20，
  
  收稿日期：2017-4-10，
  
  修回日期：2017-6-18，
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刘鑫, 郑晓慧, 刘小青, 赵瑞颖, 赵体鹏, 刘琛阳, 孙平川, 陈尔强. 聚(乙烯基对苯二甲酸二烷基酯)的非寻常相转变[J]. 高分子学报, 2017,(9):1506-1516.

Xin Liu, Xiao-hui Zheng, Xiao-qing Liu, Rui-ying Zhao, Ti-peng Zhao, Chen-yang Liu, Ping-chuan Sun, Er-qiang Chen. Unusual Phase Transition of Poly(di(alkyl) vinylterephthalates)[J]. Acta Polymerica Sinica, 2017,(9):1506-1516.
刘鑫, 郑晓慧, 刘小青, 赵瑞颖, 赵体鹏, 刘琛阳, 孙平川, 陈尔强. 聚(乙烯基对苯二甲酸二烷基酯)的非寻常相转变[J]. 高分子学报, 2017,(9):1506-1516. DOI： 10.11777/j.issn1000-3304.2017.17082.

Xin Liu, Xiao-hui Zheng, Xiao-qing Liu, Rui-ying Zhao, Ti-peng Zhao, Chen-yang Liu, Ping-chuan Sun, Er-qiang Chen. Unusual Phase Transition of Poly(di(alkyl) vinylterephthalates)[J]. Acta Polymerica Sinica, 2017,(9):1506-1516. DOI： 10.11777/j.issn1000-3304.2017.17082.

摘要

以聚（乙烯基对苯二甲酸二烷基酯）（PDAVT）为对象，用热分析、X射线衍射、流变及固体核磁共振等方法考察了甲壳型液晶高分子中存在的“低温无序、高温有序”的非寻常相行为.实验证明，在升温过程中，烷基基团为丁基、己基和辛基的PDAVT（P4、P6和P8）可从无定形态发育出柱状（Col）液晶相，导致在高温区体系模量升高.降温时P6和P8可完全回到无定形态，表现出典型的“各向同性相重入”行为.PDAVT液晶相畴的生长具有一维生长的特点，是成核控制的，升高温度可加快Col相的形成.固体核磁共振实验表明，样品从无定形态转变为Col相的过程与侧链运动性的不断加强有密切关系.我们也初步探索了剪切场或拉伸场对液晶转变的影响，发现当温度不高时，剪切或拉伸既不改变液晶转变温度，也没有提高液晶态样品的液晶化程度.综合分析多方面的实验结果可以看出，PDAVT的非寻常相行为是熵主导的.侧链的加速运动会增强“甲壳效应”，Col相是侧链熵最大化的结果.

Abstract

An unusual phase behavior

showing the disordered phase at low temperatures and the ordered phase at high temperatures

which is known as the "isotropic phase reentry"

has been observed in mesogen-jacketed liquid crystalline polymers and other side-chain jacketed polymers

for example

in some poly(di(alkyl) vinylterephthalates) (PDAVTs). In general

such a phase behavior is considered entropy dominant. However

the mechanism underneath is not fully addressed yet. Here

we study in detail the feature of phase transition of the PDAVT samples with the alkyl group of butyl

hexyl and octyl (denoted as P4

P6 and P8

respectively) by differential scanning calorimetry (DSC)

X-ray diffraction (XRD)

rheology

and solid-state NMR. Undetectable in DSC experiment

the columnar liquid crystalline (Col) phase formation is demonstrated by XRD upon heating the PDAVT samples from isotropic state. It is also evidenced by rheology measurement

showing that

after glass transition

the samples have their shear storage modulus increased by two orders of magnitude at high temperature. Upon cooling

P4 retains its Col phase probably due to the molecular motion frozen by glass transition

while P6 and P8

which have quite low glass transition temperature (

)

can fully return to the isotropic state

exhibiting the typical behavior of "isotropic phase reentry". It is found that the Col phase formation is nucleation-limited

with the feature of one-dimensional growth. At higher temperature

the nucleation barrier is drastically reduced

resulting in a much faster growth rate of Col phase. Sufficient development of the Col phase at the temperature above

makes the samples solid-like. Solid-sate NMR experiment reveals that increasing the temperature activates the alkyl tail motion first

which in fact triggers the Col phase formation. Effects of shearing and stretching on the Col phase formation are further examined. It is found that the external fields applied cannot induce the isotropic-to-Col transition of PDAVT when the temperature is close to the transition temperature

although the PDAVT chains can be oriented to some extent. On the basis of the experimental data obtained using these techniques

we conclude that the maximization of side-chain entropy is the driving force for the isotropic-to-Col phase transition. Namely

only at sufficiently high temperature can the strong side-chain motion enhance the "side-chain jacketing" effect

making the chains more rod-like which will pack parallelly to form the Col phase.

关键词

甲壳效应柱状液晶相各向同性相重入熵致有序

Keywords

Jacketing effectColumnar liquid crystalline phaseIsotropic phase reentryEntropy driven ordering

references

Qifeng Zhou , Xinjiu Wang . Liquid Crystalline Polymers , : Beijing Science Press , 1994 . 214 - 258.

周其凤 , 王新久 . 液晶高分子 , : 北京科学出版社 , 1994 . 214 - 258.

A Donald , A Windle , S Hanna . Liquid Crystalline Polymers , : Cambridge Cambridge University Press , 2006 . 504 - 543.

H Finkelmann , M Happ , M Portugal , H Ringsdorf . . Makromol Chem , 1978 . 179 2541 - 2544 . DOI:10.1002/macp.1978.021791018http://doi.org/10.1002/macp.1978.021791018.

Dierking I. Textures of Liquid Crystals. New Jersey:John Wiley & Sons, 2006. 1-20

Q F Zhou , H M Li , X D Feng . . Macromolecules , 1987 . 20 233 - 234 . DOI:10.1021/ma00167a042http://doi.org/10.1021/ma00167a042.

X F Chen , Z H Shen , X H Wan , X H Fan , E Q Chen , Y Ma , Q F Zhou . . Chem Soc Rev , 2010 . 39 3072 - 3101 . DOI:10.1039/b814540ghttp://doi.org/10.1039/b814540g.

Xiaofang Chen , Zhihao Shen , Erqiang Chen , Xinhua Wan , Xinghe Fan , Qifeng Zhou . . Scientia Sinica Chimica , 2012 . 42 606 - 621 . http://kns.cnki.net/KCMS/detail/detail.aspx?filename=jbxk201205005&dbname=CJFD&dbcode=CJFQ.

陈小芳 , 沈志豪 , 陈尔强 , 宛新华 , 范星河 , 周其凤 . . 中国科学:化学 , 2012 . 42 606 - 621 . http://kns.cnki.net/KCMS/detail/detail.aspx?filename=jbxk201205005&dbname=CJFD&dbcode=CJFQ.

C Ye , H L Zhang , Y Huang , E Q Chen , Y L Lu , D Y Shen , X H Wan , Z H Shen , S Z Cheng , Q F Zhou . . Macromolecules , 2004 . 37 ( 19 ): 7188 - 7196 . DOI:10.1021/ma049195bhttp://doi.org/10.1021/ma049195b.

Y F Zhao , X H Fan , X H Wan , X F Chen , Y Yi , L Wang , X Dong , Q Zhou . . Macromolecules , 2006 . 39 948 - 956 . DOI:10.1021/ma0514370http://doi.org/10.1021/ma0514370.

S Chen , C Jie , H L Xie , H L Zhang . . J Polym Sci, Part A:Polym Chem , 2012 . 50 3923 - 3935 . DOI:10.1002/pola.v50.19http://doi.org/10.1002/pola.v50.19.

X Q Liu , J Wang , S Yang , Y F Men , P C Sun , E Q Chen . . Polymer , 2016 . 87 260 - 267 . DOI:10.1016/j.polymer.2016.02.012http://doi.org/10.1016/j.polymer.2016.02.012.

P Barny , J Dubols , C Friedrich , C Noel . . Polym Bull , 1986 . 15 341 - 348 . DOI:10.1007/BF00254853http://doi.org/10.1007/BF00254853.

V Percec , M Lee . . J Mater Chem , 1991 . 1 1007 - 1014 . DOI:10.1039/JM9910101007http://doi.org/10.1039/JM9910101007.

L Noirez , P Keller , P Davidson , F Hardouin , J P Cotton . . J Phys Fr , 1988 . 49 1993 - 1999 . DOI:10.1051/jphys:0198800490120199300http://doi.org/10.1051/jphys:0198800490120199300.

W G Bouwman , W H de Jeu . . Liq Cryst , 1994 . 16 853 - 856 . DOI:10.1080/02678299408027855http://doi.org/10.1080/02678299408027855.

H L Tu , D Zhang , X H Wan , X F Chen , Y X Liu , H L Zhang , Q F Zhou . . Macromol Rapid Commum , 1999 . 20 549 - 551 . DOI:10.1002/(ISSN)1521-3927http://doi.org/10.1002/(ISSN)1521-3927.

H L Tu , X H Wan , Y X Liu , X F Chen , D Zhang , Q F Zhou , Z H Shen , J J Ge , S Jin , S Z Cheng . . Macromolecules , 2000 . 33 6315 - 6320 . DOI:10.1021/ma991768ahttp://doi.org/10.1021/ma991768a.

X Y Yin , E Q Chen , X H Wan , Q F Zhou . . Chinese J Polym Sci , 2003 . 21 9 - 14.

X Y Yin , C Ye , X Ma , E Q Chen , X Y Qi , X Duan , X H Wan , S Z Cheng , Q F Zhou . . J Am Chem Soc , 2003 . 125 6854 - 6855 . DOI:10.1021/ja034462zhttp://doi.org/10.1021/ja034462z.

S Z D Cheng , Transitions in Polymers:the Role of Metastable States Phase . . Amsterdam:Elsevier Science , 2008 . 37 - 39.

B Wunderlich . Macromolecular Physics , Vol. 2 : New York Academic Press , 1976 . 132 - 147.

Y G Lin , D T Mallin , J Chien , H H Winter . . Macromolecules , 1991 . 24 850 - 854 . DOI:10.1021/ma00004a006http://doi.org/10.1021/ma00004a006.

H W Richtering , K D Gagnon , R W Lenz , R C Fuller , H H Winter . . Macromolecules , 1992 . 25 2429 - 2433 . DOI:10.1021/ma00035a021http://doi.org/10.1021/ma00035a021.

L Li , Y Aoki . . Macromolecules , 1997 . 30 7835 - 7841 . DOI:10.1021/ma971045whttp://doi.org/10.1021/ma971045w.

C Y Liu , J Zhang , J S He , G H Hu . . Polymer , 2003 . 44 7529 - 7532 . DOI:10.1016/j.polymer.2003.09.013http://doi.org/10.1016/j.polymer.2003.09.013.

P C Sun , Q Q Dang , B H Li , T H Chen , Y N Wang , H Lin , Q H Jin , D D Ding , A C Shi . . Macromolecules , 2005 . 38 5654 - 5667 . DOI:10.1021/ma0505979http://doi.org/10.1021/ma0505979.

S Sun , H Tang , P Y Wu . . Phys Chem Chem Phys , 2009 . 11 9861 - 9870 . DOI:10.1039/b909914jhttp://doi.org/10.1039/b909914j.

P J Flory . . Proc R Soc Lond , 1956 . A234 73 - 89.

L Onsager , N Y Ann . . Acad Sci , 1949 . 51 627 - 659 . DOI:10.1111/nyas.1949.51.issue-4http://doi.org/10.1111/nyas.1949.51.issue-4.

C Y Liu , J S He , E Van Ruymbeke , R Keunings , C Bailly . . Polymer , 2006 . 47 4461 - 4479 . DOI:10.1016/j.polymer.2006.04.054http://doi.org/10.1016/j.polymer.2006.04.054.

F Y Liu , F Y Li , G H Deng , Y M Chen , B Q Zhang , J Zhang , C Y Liu . . Macromolecules , 2012 . 45 1636 - 1645 . DOI:10.1021/ma202461ehttp://doi.org/10.1021/ma202461e.

X Liu , R Y Zhao , T P Zhao , C Y Liu , S Yang , E Q Chen . . RSC Adv , 2014 . 4 18431 - 18441 . DOI:10.1039/C4RA01652Ahttp://doi.org/10.1039/C4RA01652A.

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