Triblock Copolymers as Templates in Mesoporous Silica Formation:  Structural Dependence on Polymer Chain Length and Synthesis Temperature

Langmuir ◽  
2001 ◽  
Vol 17 (17) ◽  
pp. 5398-5402 ◽  
Author(s):  
Pius Kipkemboi ◽  
Andrew Fogden ◽  
Viveka Alfredsson ◽  
Katarina Flodström
2021 ◽  
Vol 155 (3) ◽  
pp. 034701
Author(s):  
Emily Y. Lin ◽  
Amalie L. Frischknecht ◽  
Karen I. Winey ◽  
Robert A. Riggleman

Langmuir ◽  
2021 ◽  
Author(s):  
Hyeong Jin Kim ◽  
Wenjie Wang ◽  
Honghu Zhang ◽  
Guillaume Freychet ◽  
Benjamin M. Ocko ◽  
...  

Polymers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1516
Author(s):  
Dongmei Liu ◽  
Kai Gong ◽  
Ye Lin ◽  
Tao Liu ◽  
Yu Liu ◽  
...  

We investigated the interfacial properties of symmetric ternary An/AmBm/Bn and An/Am/2BmAm/2/Bn polymeric blends by means of dissipative particle dynamics (DPD) simulations. We systematically analyzed the effects of composition, chain length, and concentration of the copolymers on the interfacial tensions, interfacial widths, and the structures of each polymer component in the blends. Our simulations show that: (i) the efficiency of the copolymers in reducing the interfacial tension is highly dependent on their compositions. The triblock copolymers are more effective in reducing the interfacial tension compared to that of the diblock copolymers at the same chain length and concentration; (ii) the interfacial tension of the blends increases with increases in the triblock copolymer chain length, which indicates that the triblock copolymers with a shorter chain length exhibit a better performance as the compatibilizers compared to that of their counterparts with longer chain lengths; and (iii) elevating the triblock copolymer concentration can promote copolymer enrichment at the center of the interface, which enlarges the width of the phase interfaces and reduces the interfacial tension. These findings illustrate the correlations between the efficiency of copolymer compatibilizers and their detailed molecular parameters.


2003 ◽  
Vol 332 (1-3) ◽  
pp. 199-206 ◽  
Author(s):  
Nobuaki Kitazawa ◽  
Hideyoshi Namba ◽  
Masami Aono ◽  
Yoshihisa Watanabe

2019 ◽  
Vol 28 (2) ◽  
pp. 77-88
Author(s):  
Yongji Gong ◽  
Weihua Song ◽  
Yifan Wu ◽  
Daohai Zhang ◽  
Yufei Liu ◽  
...  

The poly(l-lactide-b-ethylene glycol-b-l-lactide) (PLLA-PEG-PLLA) triblock copolymers with different chain segment length are fabricated by ring-opening polymerization. The structure, molecular weight, and crystallization behaviors of the triblock copolymers are characterized by Fourier transform infrared, nuclear magnetic resonance spectroscopy, gel permeation in chromatography, X-ray diffraction, differential scanning calorimetry, and polarizing optical microscopy (POM). The results show that the increase of block length is beneficial to improve its crystallization. In addition, the triblock copolymer exhibits a double crystallization phenomenon. The POM results indicate that PEG and PLLA chains of the copolymer crystallize in their respective crystallization temperature regions. The growth rate of the PLLA spherocrystal decreases and the dendritic spherocrystals appear with increasing the PEG chain length when the PLLA chain of the copolymer is isothermal crystallized at 80°C and PLLA chain length is constant. The growth rate of the PEG spherocrystal decreases and the spherocrystal morphology changes little with increasing PLLA chain length when the PEG chain is isothermal crystallized at 25°C and the length of PEG chain remained unchanged.


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