Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Polymers (Basel) ; 13(23)2021 Nov 28.
Artigo em Inglês | MEDLINE | ID: mdl-34883671

RESUMO

An approach to obtaining various nanostructures utilizing a well-studied polystyrene-b-poly(isoprene) or PS-b-PI diblock copolymer system through chemical modification reactions is reported. The complete hydrogenation and partial sulfonation to the susceptible carbon double bonds of the PI segment led to the preparation of [polystyrene-b-poly(ethylene-alt-propylene)] as well as [polystyrene-b-poly(sulfonated isoprene-co-isoprene)], respectively. The hydrogenation of the polyisoprene block results in enhanced segmental immiscibility, whereas the relative sulfonation induces an amphiphilic character in the final modified material. The successful synthesis of the pristine diblock copolymer through anionic polymerization and the relative chemical modification reactions were verified using several molecular and structural characterization techniques. The thin film structure-properties relationship was investigated using atomic force microscopy under various conditions such as different solvents and annealing temperatures. Small-angle X-ray scattering was employed to identify the different observed nanostructures and their evolution upon thermal annealing.

2.
Polymers (Basel) ; 13(14)2021 Jul 14.
Artigo em Inglês | MEDLINE | ID: mdl-34301065

RESUMO

A novel approach to obtaining nanocomposite materials using anionic sequential polymerization and post-synthetic esterification reactions with chemically modified graphene sheets (CMGs) is reported. The anionically synthesized diblock copolymer precursors of the PS-b-PI-OH type were grafted to the chemically modified -COOH groups of the CMGs, giving rise to the final composite materials, namely polystyrene-b-poly(isoprene)-g-CMGs, which exhibited enhanced physicochemical properties. The successful synthesis was determined through multiple molecular characterization techniques together with thermogravimetric analysis for the verification of increased thermal stability, and the structure/properties relationship was justified through transmission electron microscopy. Furthermore, the arrangement of CMGs utilizing lamellar and cylindrical morphologies was studied in order to determine the effect of the loaded CMGs in the adopted topologies.

3.
Molecules ; 25(24)2020 Dec 19.
Artigo em Inglês | MEDLINE | ID: mdl-33352785

RESUMO

To the best of our knowledge, this is the very first time that a thorough study of the synthetic procedures, molecular and thermal characterization, followed by structure/properties relationship for symmetric and non-symmetric second generation (2-G) dendritic terpolymers is reported. Actually, the synthesis of the non-symmetric materials is reported for the first time in the literature. Anionic polymerization enables the synthesis of well-defined polymers that, despite the architecture complexity, absolute control over the average molecular weight, as well as block composition, is achieved. The dendritic type macromolecular architecture affects the microphase separation, because different morphologies are obtained, which do not exhibit long range order, and various defects or dislocations are evident attributed to the increased number of junction points of the final material despite the satisfactory thermal annealing at temperatures above the highest glass transition temperature of all blocks. For comparison reasons, the initial dendrons (miktoarm star terpolymer precursors) which are connected to each other in order to synthesize the final dendritic terpolymers are characterized in solution and in bulk and their self-assembly is also studied. A major conclusion is that specific structures are adopted which depend on the type of the core connection between the ligand and the active sites of the dendrons.


Assuntos
Dendrímeros/química , Polímeros/química , Polimerização , Temperatura
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...