Cited by 553Block Copolymer Self-AssemblyPolymer crystallization and propertiesMesoporous Materials and Catalysis

Ordered Nanoporous Polymers from Polystyrene−Polylactide Block Copolymers

Zalusky, Andrew S., Olayo-Valles, Roberto, Wolf, Johanna H., Hillmyer, Marc A.·2002·Journal of the American Chemical Society

Abstract

Nanoporous polystyrene monoliths were prepared from polystyrene-polylactide (PS-PLA) block copolymers that form hexagonally packed nanocylinders of PLA in a PS matrix. A morphology diagram was developed to determine the range in composition and molecular weight over which this morphology existed. Macroscopic alignment of these materials gave anisotropic monoliths that were subjected to mild degradation conditions leading to the chemical etching of the PLA. The resulting nanoporous monoliths consisted of a polystyrene matrix containing hexagonally close-packed, oriented, and continuous nanoscopic channels (pore size was tunable through synthesis or blending) lined with chemically accessible hydroxyl functional groups. Both the precursors and the porous materials were analyzed moleculary (size-exclusion chromatography and proton nuclear magnetic resonance spectroscopy) and structurally (small-angle X-ray scattering, scanning electron microscopy, and differential scanning calorimetry). In addition, the surface area and pore size distribution of the nanoporous monoliths were characterized (N2 adsorption measurements). These nanoporous materials have remarkable potential as hosts for nanomaterial synthesis, size-selective catalyst supports, and advanced separations.

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Crossref · 10.1021/ja0278584

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  • Since the hard block is poly(lactide), at a fixed molar mass, decreasing the polarity of the midblock segment effectively increases the segregation strength of the two blocks.

    “Since in this work the hard block is poly(lactide), at a fi xed molar mass, decreasing the polarity of the midblock segment e ff ectively increases the segregation strength of the two blocks. 11,13,64,85 -89”

    From Aliphatic Polyester Block Polymer Design (2016) · cites this paper as [89]

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Authors
Zalusky, A. S., Olayo-Valles, R., Wolf, J. H., & Hillmyer, M. A.
Affiliations
  • University of Minnesota (US)
  • Contribution from the Department of Chemistry, University of Minnesota, 207 Pleasant Street SE, Minneapolis, Minnesota 55455-0431
Venue
Journal of the American Chemical Society
Published
2002-10-01
Volume
124
Issue
43
Pages
12761-12773
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2106756509
Cited by
553
References
2
Citations by year
2026: 8 · 2025: 12 · 2024: 7 · 2023: 19 · 2022: 27 · 2021: 14 · 2020: 22 · 2019: 13 · 2018: 24 · 2017: 27 · 2016: 24 · 2015: 23 · 2014: 30 · 2013: 37 · 2012: 41
FWCI
13.09
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of the American Chemical Society (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Physical Sciences › Materials Science › Materials Chemistry › Block Copolymer Self-Assembly
  • Physical Sciences › Materials Science › Polymers and Plastics › Polymer crystallization and properties
  • Physical Sciences › Materials Science › Materials Chemistry › Mesoporous Materials and Catalysis
Keywords
nanoporous polymers, block copolymer self-assembly, morphology diagram, chemical etching, tunable pore size, hydroxyl groups, catalyst supports, size-selective separation

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