Molar-mass dependence of the lamellar thickness in symmetric diblock copolymers

1994 ◽  
Vol 16 (7) ◽  
pp. 835-842 ◽  
Author(s):  
C. M. Papadakis ◽  
K. Almdal ◽  
D. Posselt
2021 ◽  
pp. 110537
Author(s):  
Birsen Somuncuoğlu ◽  
Yu Lin Lee ◽  
Anna P. Constantinou ◽  
David L. M. Poussin ◽  
Theoni K. Georgiou

2019 ◽  
Vol 8 (12) ◽  
pp. 1594-1598 ◽  
Author(s):  
Mingchen Jia ◽  
Nikos Hadjichristidis ◽  
Yves Gnanou ◽  
Xiaoshuang Feng

2000 ◽  
Vol 151 (1) ◽  
pp. 459-464
Author(s):  
J.A.M. De Brouwer ◽  
J.J.G.S. Van Es ◽  
A.L. German

Polymers ◽  
2021 ◽  
Vol 13 (16) ◽  
pp. 2676
Author(s):  
Panagiotis G. Falireas ◽  
Bruno Ameduri

New copolymers based on vinylidene fluoride (VDF) and 2,3,3,3-tetrafluoroprop-1-ene (1234yf) were synthesized by organometallic-mediated radical copolymerization (OMRcP) using the combination of bis(tert-butylcyclohexyl) peroxydicarbonate initiator and bis(acetylacetonato)cobalt(II), (Co(acac)2) as a controlling agent. Kinetics studies of the copolymerization of the fluoroalkenes copolymers were monitored by GPC and 19F NMR with molar masses up to 12,200 g/mol and dispersities (Đ) ranging from 1.33 to 1.47. Such an OMRcP behaves as a controlled copolymerization, evidenced by the molar mass of the resulting copolymer-monomer conversion linear relationship. The reactivity ratios, ri, of both comonomers were determined by using the Fineman-Ross and Kelen-Tüdos fitting model leading to rVDF = 0.384 ± 0.013 and r1234yf = 2.147 ± 0.129 at 60 °C, showing that a lower reactivity of VDF integrated in the copolymer to a greater extent leads to the production of gradient or pseudo-diblock copolymers. In addition, the Q (0.03) and e (0.06 and 0.94) parameters were assessed, as well as the dyad statistic distributions and mean square sequence lengths of PVDF and P1234yf.


2018 ◽  
Vol 50 (11) ◽  
pp. 1043-1049 ◽  
Author(s):  
Yasuhiro Matsuda ◽  
Kazuya Okumura ◽  
Shigeru Tasaka

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