Manipulating ordering transitions in interfacially modified block copolymers

Soft Matter ◽  
2009 ◽  
Vol 5 (23) ◽  
pp. 4757 ◽  
Author(s):  
Nripen Singh ◽  
Maëva S. Tureau ◽  
Thomas H. Epps, III
Polymers ◽  
2021 ◽  
Vol 13 (20) ◽  
pp. 3579
Author(s):  
Ilsia M. Davletbaeva ◽  
Alexander Yu. Alentiev ◽  
Zulfiya Z. Faizulina ◽  
Ilnaz I. Zaripov ◽  
Roman Yu. Nikiforov ◽  
...  

Organosubstituted silica derivatives were synthesized and investigated as modifiers of block copolymers based on macroinitiator and 2,4-toluene diisocyanate. A peculiarity of the modified block copolymers is the existence in their structure of coplanar rigid polyisocyanate blocks of acetal nature (O-polyisocyanates). Organosubstituted silica derivatives have a non-additive effect on high-temperature relaxation and α-transitions of modified polymers and exhibit the ability to influence the supramolecular structure of block copolymers. The use of the developed modifiers leads to a change in the gas transport properties of block copolymers. The increase of the permeability coefficients is due to the increase of the diffusion coefficients. At the same time, the gas solubility coefficients do not change. An increase in the ideal selectivity for a number of gas pairs is observed. An increase in the selectivity for the CO2/N2 gas pair (from 25 to 39) by 1.5 times demonstrates the promising use of this material for flue gases separation.


2010 ◽  
Vol 116 (5) ◽  
pp. 3047-3055 ◽  
Author(s):  
Jorge de A. Rodrigues ◽  
Regina Sandra V. Nascimento

2011 ◽  
Vol 125 (3) ◽  
pp. 382-385 ◽  
Author(s):  
N.A. Yufa ◽  
S.L. Fronk ◽  
S.J. Rosenthal ◽  
Seth B. Darling ◽  
W.A. Lopes ◽  
...  

2002 ◽  
Vol 724 ◽  
Author(s):  
Elizabeth R. Wright ◽  
R. Andrew McMillan ◽  
Alan Cooper ◽  
Robert P. Apkarian ◽  
Vincent P. Conticello

AbstractTriblock copolymers have traditionally been synthesized with conventional organic components. However, triblock copolymers could be synthesized by the incorporation of two incompatible protein-based polymers. The polypeptides would differ in their hydrophobicity and confer unique physiochemical properties to the resultant materials. One protein-based polymer, based on a sequence of native elastin, that has been utilized in the synthesis of biomaterials is poly (Valine-Proline-Glycine-ValineGlycine) or poly(VPGVG) [1]. This polypeptide has been shown to have an inverse temperature transition that can be adjusted by non-conservative amino acid substitutions in the fourth position [2]. By combining polypeptide blocks with different inverse temperature transition values due to hydrophobicity differences, we expect to produce amphiphilic polypeptides capable of self-assembly into hydrogels. Our research examines the design, synthesis and characterization of elastin-mimetic block copolymers as functional biomaterials. The methods that are used for the characterization include variable temperature 1D and 2D High-Resolution-NMR, cryo-High Resolutions Scanning Electron Microscopy and Differential Scanning Calorimetry.


Author(s):  
Mark J. Newman ◽  
Jeffrey K. Actor ◽  
Mannersamy Balusubramanian ◽  
Chinnaswamy Jagannath
Keyword(s):  

2019 ◽  
Author(s):  
Jacob Ishibashi ◽  
Yan Fang ◽  
Julia Kalow

<p>Block copolymers are used to construct covalent adaptable networks that employ associative exchange chemistry (vitrimers). The resulting vitrimers display markedly different nanostructural, thermal and rheological properties relative to those of their statistical copolymer-derived counterparts. This study demonstrates that prepolymer sequence is a versatile strategy to modify the properties of vitrimers.</p>


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