scholarly journals Crystalline modification of a rare earth nucleating agent for isotactic polypropylene based on its self-assembly

2018 ◽  
Vol 5 (5) ◽  
pp. 180247 ◽  
Author(s):  
Yuanming Zhang ◽  
Tingting Sun ◽  
Wei Jiang ◽  
Guangting Han

In this paper, the crystalline modification of a rare earth nucleating agent (WBG) for isotactic polypropylene (PP) based on its supramolecular self-assembly was investigated by differential scanning calorimetry, wide-angle X-ray diffraction and polarized optical microscopy. In addition, the relationship between the self-assembly structure of the nucleating agent and the crystalline structure, as well as the possible reason for the self-assembly behaviour, was further studied. The structure evolution of WBG showed that the self-assembly structure changed from a needle-like structure to a dendritic structure with increase in the content of WBG. When the content of WBG exceeded a critical value (0.4 wt%), it self-assembled into a strip structure. This revealed that the structure evolution of WBG contributed to the K β and the crystallization morphology of PP with different content of WBG. In addition, further studies implied that the behaviour of self-assembly was a liquid–solid transformation of WBG, followed by a liquid–liquid phase separation of molten isotactic PP and WBG. The formation of the self-assembly structure was based on the free molecules by hydrogen bond dissociation while being heated, followed by aggregation into another structure by hydrogen bond association while being cooled. Furthermore, self-assembly behaviour depends largely on the interaction between WBG themselves.

Polymers ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 1777 ◽  
Author(s):  
Li ◽  
Xin ◽  
Song ◽  
Dong ◽  
Ben ◽  
...  

In this paper, the crystalline modification of isotactic polypropylene (PP) with a rare earth β nucleating agent (WBG) with different ultrasound conditions was investigated by scanning electron microscopy (SEM), wide-angle X-ray diffraction (XRD), and differential scanning calorimetry (DSC). The relationship between the ultrasound conditions and the crystalline structure, as well as the mechanism for the behavior, were revealed. SEM showed that the dispersion of the nucleating agent in the PP matrix was better at shorter ultrasound distances. In addition, the higher the water cooling temperature, the better the nucleating agent was dispersed in the PP matrix. The results of XRD and DSC showed that the crystallinity and the relative content of the β-crystal were increased with nearer ultrasound distance, as well as increased in higher water cooling temperatures. In particular, under the same conditions, the crystallinity and the relative content of the β-crystal after ultrasonic treatment were much higher than those without ultrasound.


2016 ◽  
Vol 499 ◽  
pp. 70-75
Author(s):  
Zhongping Wang ◽  
Feifei Xiang ◽  
Yan Lu ◽  
Sheng Wei ◽  
Chao Li ◽  
...  

2019 ◽  
Vol 25 (71) ◽  
pp. 16288-16293 ◽  
Author(s):  
Hui Li ◽  
Yidan Shen ◽  
Peng Yang ◽  
Jennifer E. S. Szymanowski ◽  
Jiahui Chen ◽  
...  

e-Polymers ◽  
2016 ◽  
Vol 16 (4) ◽  
pp. 343-349 ◽  
Author(s):  
Ya-Juan Su ◽  
Ze-Xin Ma ◽  
Jian-Hua Huang

AbstractDissipative particle dynamics simulations are performed to study the self-assembly of rod-coil (RC) diblock copolymers confined in a slit with two coil-selective surfaces. The effect of rod length and slit thickness on the assembly structure is investigated. A morphological phase diagram as a function of slit thickness and rod length is presented. We observe several ordered structures, such as perpendicular cylinders, parallel cylinders, and puck-shaped structure. In the assembly structures, long-range rod-rod orientational order is observed when the rod length exceeds a critical rod length. Our results show that the coil-selective slit influences the assembly structure as well as the rod orientation of RC diblock copolymers.


RSC Advances ◽  
2016 ◽  
Vol 6 (82) ◽  
pp. 78385-78395 ◽  
Author(s):  
Paul Joyce ◽  
Timothy J. Barnes ◽  
Ben J. Boyd ◽  
Clive A. Prestidge

Combining 1H NMR and sSAXS to discriminate the speciation and structure evolution of lipolysis products for submicron lipid droplets and lipid loaded in porous silica particles.


2013 ◽  
Vol 135 (47) ◽  
pp. 17723-17726 ◽  
Author(s):  
Amber M. Johnson ◽  
Michael C. Young ◽  
Xing Zhang ◽  
Ryan R. Julian ◽  
Richard J. Hooley

2017 ◽  
Vol 24 (Supp02) ◽  
pp. 1850025
Author(s):  
YUFEN HU ◽  
WEI LI ◽  
YAN LU ◽  
ZHONGPING WANG ◽  
XINLI LENG ◽  
...  

The self-assembly structures of 2,2[Formula: see text]:6[Formula: see text],2[Formula: see text]-terpyridine-4[Formula: see text]-carboxylic acid (C[Formula: see text]H[Formula: see text]N3O2; [Formula: see text]) molecules and 3,5-diphenylbenzoic acid (C[Formula: see text]H[Formula: see text]O2; [Formula: see text]) molecules on Ag(110) surface have been investigated by scanning tunneling microscopy (STM) and Density Functional Theory (DFT) calculation. The [Formula: see text] molecules form two different well-organized structures due to the [Formula: see text]–[Formula: see text] stacking and dipole–dipole interactions. When three C atoms of [Formula: see text] molecules are replaced by three N atoms to form [Formula: see text] molecules, the main driving force to form ordered assembly structures of [Formula: see text] molecule is changed to metal–organic coordination bond and hydrogen bond. The dramatic changes of main driving force between [Formula: see text]/Ag(110) and [Formula: see text]/Ag(110) system demonstrate that the N atoms are apt to form metal–organic coordination bond and hydrogen bond but dipole–dipole interactions and [Formula: see text]–[Formula: see text] stacking are relative to C atoms. These findings further reveal that the optimization design of organic molecules could vary the main driving force and then lead to the change of the molecular self-assembly structures.


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