Sentence examples for block copolymers consisting of from inspiring English sources

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The preparation of block copolymers consisting of poly(4-vinylpyridine) (P4VP) by atom transfer radical polymerization (ATRP) was investigated.

We developed block copolymers consisting of PBAE oligomer center units and poly ethylene glycol) (PEG) end units.

Well-defined statistical, gradient and block copolymers consisting of isobornyl acrylate (IBA) and n-butyl acrylate (nBA) were synthesized via atom transfer radical polymerization (ATRP).

The block copolymers consisting of 2,7-dimethoxycarbazole- and oxadiazole-containing segments as hole and electron transporting units, respectively, were synthesized by NMRP manner.

New temperature sensitive AB, ABA, and BAB amphiphilic block copolymers consisting of hydrophilic poly ethylene oxide) and hydrophobic poly ethyl glycidyl carbamate) blocks were synthesized by anionic polymerization followed by chemical modification reactions.

Block copolymers consisting of rubbery lignin derivative components (i.e. hydroxypropyl lignin, L) and cellulose propionate (CP) segments ranging in size from degree of polymerization (DP) 5 to 60 were synthesized using chemistry described previously.

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The dynamic mechanical response of block copolymers consisted of separate PIB and PS relaxations whose relative intensities scaled well with copolymer composition.

These block copolymers consisted of polystyrene as the hard block, n-butyl acrylate (BA) as soft block and terpyridine units as the ligand moiety placed at different locations in the soft block.

The block copolymers consist of a linear hydrophobic polyoxypropylene (PPO) block with hydrophilic polyoxyethylene (PEO) blocks on each side with the structure PEO-PPO-PEO.

Block copolymers consist of two chemically dissimilar long molecules joined end-to-end, depicted as red and blue in Fig. 3.

Block copolymers consist of two or more different types of polymers covalently attached to one another, and they can self-assemble into specific structures based on the competition between the free energy of mixing and entropy of the chains [ 46].

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