Anhydride structures affect the acylation modification and emulsion stabilization ability of mammalian and fish gelatins

2021 ◽  
pp. 131882
Author(s):  
Ting Zhang ◽  
Jiamin Xu ◽  
Shudan Huang ◽  
Ningping Tao ◽  
Xichang Wang ◽  
...  
2008 ◽  
Vol 20 (17) ◽  
pp. 3239-3243 ◽  
Author(s):  
Jin-Woong Kim ◽  
Daeyeon Lee ◽  
Ho Cheung Shum ◽  
David A. Weitz

2015 ◽  
Vol 47 (5) ◽  
pp. 408-412 ◽  
Author(s):  
Eisuke Baba ◽  
Toshiaki Yatsunami ◽  
Takuya Yamamoto ◽  
Yasuyuki Tezuka

2019 ◽  
Vol 1 ◽  
pp. 17-23 ◽  
Author(s):  
Andrew Hirsch ◽  
Young-Hee Cho ◽  
Yuan H.Brad Kim ◽  
Owen G. Jones

1989 ◽  
Vol 40 ◽  
pp. 93-105 ◽  
Author(s):  
Helen Hassander ◽  
Beatrice Johansson ◽  
Bertil Törnell

1969 ◽  
Vol 17 (3) ◽  
pp. 91-100 ◽  
Author(s):  
E.J. Birr ◽  
C. Bertolotto ◽  
G. Cibrario ◽  
C. Bertolotto

1991 ◽  
Vol 248 ◽  
Author(s):  
C. Yeung ◽  
Anna C. Balazs ◽  
David Jasnow

The presence of copolymers at an interface between two immiscible fluids is crucial to such processes as emulsion stabilization and microemulsion formation [1]. Recently Marques and Joanny [2] and Garel et al. [3] have studied the behavior of a random copolymer at a liquid-liquid interface. However, the arrangement or sequence distribution of the monomers in a copolymer can vary widely from random to blocky or purely alternating. In this paper, we use both analytic arguments and molecular dynamics simulations to determine how the sequence distribution affects the adsorption and conformation of a single macromolecule at the boundary between two immiscible fluids [4]. In particular, we derive an expression for the free energy of a copolymer at the interface and compare the resulting predictions with the outcome of the simulations. Our findings yield design criteria for fabricating polymers that display the desired interfacial properties.


2017 ◽  
Vol 27 (5) ◽  
pp. 518-520 ◽  
Author(s):  
Marina Yu. Koroleva ◽  
Andrey M. Tokarev ◽  
Evgeny V. Yurtov

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