Synthesis and microphase separation of polystyrene-b -polylactide block copolymers aimed at preparation of ordered nanoparticle/block copolymer hybrid materials

2014 ◽  
Vol 63 (7) ◽  
pp. 1159-1167 ◽  
Author(s):  
Xiaodong Hou ◽  
Qiaobo Li ◽  
Amin Cao
Author(s):  
Lee M. Trask ◽  
Nacu Hernandez ◽  
Eric W. Cochran

This article explores the dynamics, thermodynamics, and small-angle scattering of block copolymers. The goal is to determine what drives the applications of block copolymers, i.e. how block copolymers behave and how they are characterized. The article begins with a summary of the experimental data and various theories that comprise our understanding of block copolymer thermodynamics, with particular emphasis on phase behavior and especially the theory of microphase separation. It then considers topics related to block copolymer dynamics, including diffusion, viscoelasticity and rheology, shear-processing, and the kinetics of self-assembly. It also discusses small-angle scattering techniques as applied to block copolymer characterization, including scattering from ordered block copolymer melts.


1989 ◽  
Vol 177 ◽  
Author(s):  
M. Olvera de la Cruz

ABSTRACTThe ability to produce block copolymers has led to new materials with unique properties. The chemical connectivity of incompatible blocks forces segregation to occur at distances of the order of the block sizes. In block copolymer melts, the segregated domains form periodic ordered structures called microphases. Most block copolymers are strongly incompatible. In such cases, in order to ensure equilibrium microphase separated samples, the microphases are prepared from solution. Microphase separation in semidilute solutions of block copolymers in nonselective good solvent is analyzed. The solvent effects on the thermodynamics in the weak segregation limit are discussed. The concentration of block copolymer at the transition in good solvents, scales as φtN−.62and in ϑ solvents as N−.5. The transitions between microphase morphologies as a function of block copolymer concentration are studied.


2017 ◽  
Vol 46 (3) ◽  
pp. 569-585 ◽  
Author(s):  
Dechao Niu ◽  
Yongsheng Li ◽  
Jianlin Shi

Silica/organosilica cross-linked block copolymer micelles are a novel class of hybrid materials that combine the advantages of amphiphilic block copolymers and silica/organosilica cross-linking agents into one unit. This Tutorial Review summarizes the recent progress in the design, synthesis and biomedical applications of various silica/organosilica cross-linked block copolymer micelles.


Nanoscale ◽  
2021 ◽  
Author(s):  
Burhannudin Sutisna ◽  
Stoffel D. Janssens ◽  
Alessandro Giussani ◽  
David Vázquez-Cortés ◽  
Eliot Fried

Coassembly between block copolymers and nanodiamonds (NDs) leads to transparent UV-protective coatings and hybrid superstructures with hierarchical assembly of NDs.


1969 ◽  
Vol 22 (8) ◽  
pp. 1649 ◽  
Author(s):  
JR Urwin

Binary cluster integrals or excluded volumes for chemically different segment pairs in block copolymers of poly(isoprene : styrene) have been calculated from the equation derived by Froelich and Benoit for a two- sequence block copolymer. Expansion factors have been recalculated assuming a linear relation for [η]θ with respect to composition employing published values for polystyrene and polyisoprene. The results are discussed in relation to possible conformations of block copolymers.


2000 ◽  
Vol 72 (1-2) ◽  
pp. 67-72 ◽  
Author(s):  
Keith J. Watson ◽  
Jin Zhu ◽  
SonBinh T. Nguyen ◽  
Chad A. Mirkin

Ring-opening metathesis polymerization was used to modify organic soluble gold nanoparticles with redox-active polymers. A gel-permeation chromatography study revealed that each nanoparticle is modified with approximately 11 polymer chains. Electrochemical studies of nanoparticles modified with block copolymers of two different redox-active groups revealed that each monomer is electrochemically accessible, while no current rectification was observed.


2021 ◽  
Author(s):  
Isamu Akiba ◽  
Kazuo Sakurai

AbstractBlock copolymers are well recognized as excellent nanotools for delivering hydrophobic drugs. The formulation of such delivery nanoparticles requires robust characterization and clarification of the critical quality attributes correlating with the safety and efficacy of the drug before applying to regulatory authorities for approval. Static solution scattering from block copolymers is one such technique. This paper first outlines the theoretical background and current models for analyzing this scattering and then presents an overview of our recent studies on block copolymers.


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