4.7 Article

Synthesis and Melt Self-Assembly of PS-PMMA-PLA Triblock Bottlebrush Copolymers

期刊

MACROMOLECULES
卷 47, 期 9, 页码 2864-2874

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ma500625k

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资金

  1. National Science Foundation [DMR-0846584]
  2. E.I. DuPont de Nemours Co.
  3. Dow Chemical Company
  4. Northwestern University
  5. U.S. DOE [DE-AC02-06CH11357]
  6. Division Of Materials Research
  7. Direct For Mathematical & Physical Scien [0846584] Funding Source: National Science Foundation

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Polystyrene-poly(methyl methacrylate)-polylactide (PS-PMMA-PLA) triblock bottlebrush copolymer with nearly symmetric volume fractions was synthesized by grafting from a symmetrical triblock backbone and the resulting melt was characterized by scanning electron microscopy and small-angle X-ray scattering. The copolymer backbone was prepared by sequential reversible addition fragmentation chain transfer (RAFT) polymerization of solketal methacrylate (SM), 2-(bromoisobutyryl)ethyl methacrylate (BIEM), and S-(trimethylsilyl)-4-pentyn-1-ol methacrylate (TPYM). PMMA branches were grafted by atom transfer radical polymerization from the poly(BIEM) segment, PS branches were grafted by RAFT polymerization from the poly(TPYM) block after installment of the RAFT agents, while PLA side chains were grafted from the deprotected poly(SM) block. The resulting copolymer was found to exhibit a lamellae morphology with a domain spacing of 79 nm. Differential scanning calorimetry analysis indicated that PMMA was preferentially mixing with PS while phase separating from PLA domains.

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