Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Home
Search
Quick Search
Advanced
Fulltext
Browse
Collections
Persons
My eDoc
Session History
Login
Name:
Password:
Documentation
Help
Support Wiki
Direct access to
document ID:


          Institute: MPI für Polymerforschung     Collection: MPI Polymerforschung     Display Documents



  history
ID: 60102.0, MPI für Polymerforschung / MPI Polymerforschung
Structural studies of nanophase-separated poly(2-hydroxyethyl methacrylate)-l-polyisobutylene amphiphilic conetworks by solid-state NMR and small-angle x-ray scattering
Authors:Domjan, A.; Erdödi, G.; Wilhelm, Manfred; Neidhöfer, M.; Landfester, Katharina; Ivan, B.; Spiess, Hans Wolfgang
Language:English
Date of Publication (YYYY-MM-DD):2003
Title of Journal:Macromolecules
Journal Abbrev.:Macromolecules
Volume:36
Issue / Number:24
Start Page:9107
End Page:9114
Review Status:not specified
Audience:Not Specified
Abstract / Description:Bicomponent nanophase-separated poly(2-hydroxyethyl methacrylate)-linked-polyisobutylene (PHEMA-l-PIB) amphiphilic conetworks were synthesized by radical copolymerization of methacrylate-telechelic polyisobutylene (MA-PIB-MA) and different amounts of 2-(trimethylsilyloxy)ethyl methacrylate (SEMA) followed by quantitative hydrolysis of the trimethylsilyl protecting groups. The PIB content of the resulting conetworks, determined by elemental analysis and solid-state 1H NMR under fast magic-angle spinning (MAS), varied between 17 and 63% w/w. Phase separation and morphology of these conetworks were investigated by DSC, small-angle X-ray scattering (SAXS), and for the first time by 1H spin diffusion solid-state NMR. Two Tg values were observed by DSC in all samples. The observed Tg values were close to the literature values of both homopolymers (110 °C for PHEMA and -67 °C for PIB), indicating a strong phase-separated morphology in these conetworks. Parameters were optimized for the 1H spin diffusion NMR experiments, and the measurements were carried out with six filtering cycles and a 10 μs delay between pulses at 90 °C. The NMR and SAXS measurements prove strong phase-separated morphology. The sizes of the hydrophilic (PHEMA) and hydrophobic (PIB) nanodomains were determined to be in the 5-15 nm range. The spin diffusion experiments also indicate strongly separated phases without a detectable interface with mixed components. The long period of our system seems to depend weakly on the volume fraction whereas the morphology of the nanophases depends on the volume fraction.
External Publication Status:published
Document Type:Article
Affiliations:MPI für Polymerforschung
External Affiliations:Hungarian Acad Sci, Chem Res Ctr, Inst Chem, Dept Polymer Chem & Mat Sci, Pusztaszeri U 59-67, POB 17, H-1525 Budapest, Hungary.
Identifiers:LOCALID:P-03-88
The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.