Yulu Ma

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Organization: East China University of Science and Technology
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Co-reporter:Ying Liu;Linsheng Xie;Haitao Liu;Haili Zhao ;Yunxiang Wang
Journal of Applied Polymer Science 2014 Volume 131( Issue 23) pp:
Publication Date(Web):
DOI:10.1002/app.41202

ABSTRACT

Polypropylene (PP)/polystyrene-block-poly(ethylene-co-butylenes)-block-polystyrene (SEBS)/organo-montmorillonite (OMMT) nanocomposites of varying concentrations of maleic anhydride-grafted polypropylene (PP-g-MA) were prepared by continuous mixing assisted by ultrasonic oscillation. The structure and morphology of nanocomposites were investigated by X-ray diffraction (XRD), transmission electron microscopy, and scanning electron microscopy. It was found that both PP-g-MA and ultrasonic oscillation could enhance the intercalation and exfoliation of OMMT in PP matrix. Meanwhile, the formation of PP could be induced by ultrasonic irradiation at a power of more than 540 W. Rheological properties including complex viscosity, storage, and loss modulus of nanocomposites were increased after adding PP-g-MA or ultrasonic treatment. The results of mechanical properties showed that PP-g-MA could improve the tensile strength and tensile modulus of nanocomposites, but with the sacrifice of impact strength. This problem could be improved by ultrasound due to the reduced particle size of SEBS. However, the mechanical properties would be reduced by ultrasonic treatment with higher intensity due to the polymer degradation. Therefore, the synergistic effect of both compatibilizer and ultrasound should account for the balance between toughness and stiffness of PP/SEBS/OMMT ternary nanocomposites. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 41202.

Co-reporter:Jin Sha, Ethan S. Lippmann, Jason McNulty, Yulu Ma, and Randolph S. Ashton
Biomacromolecules 2013 Volume 14(Issue 9) pp:
Publication Date(Web):August 13, 2013
DOI:10.1021/bm400900r
Multicomponent poly(ethylene glycol) (PEG) brushes (i.e., ≥2 adjacent PEG brushes) can be used to engineer culture substrates with microscale, nonfouling regions decorated with covalently immobilized ligands that mediate biospecific interactions. However, synthesizing such brushes with orthogonal immobilization chemistries to permit differential biofunctionalization is nontrivial and often requires synthesis of PEG-co-polymers. To simplify synthesis and enhance the versatility of such substrates, we developed a protocol for generating orthogonal click-functionalized multicomponent PEG brushes using sequential nucleophilic substitutions by sodium azide, ethanolamine, and propargylamine. The novel application of propargylamine-mediated substitution functionalizes PEG brushes with acetylene groups, and for the first time, ethanolamine-mediated substitution is shown to be sufficient for passivating the “living” polymer chain ends between brush synthesis steps. Thus, our multicomponent PEG brushes present dual orthogonal chemistries (i.e., azido and acetylene groups) for ligand immobilization via versatile copper-free click reactions, which are useful for in situ surface modifications during cell culture.
SODIUM;ETHENE;4-METHYL-2-METHYLIDENEPENTANOATE;2-METHYLPROP-2-ENOIC ACID