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@ARTICLE{Frielinghaus:34172,
      author       = {Frielinghaus, H. and Hermsdorf, N. and Sigel, R. and
                      Almdal, K. and Mortensen, K. and Hamley, I. W. and Messé,
                      L. and Corvazier, M. F. and Ryan, A. J. and van Dusschoten,
                      D. and Wilhelm, M. and Floudas, G. and Fytas, G.},
      title        = {{B}lends of {AB}/{BC} diblock copolymers with a large
                      interaction parameter {C}hi},
      journal      = {Macromolecules},
      volume       = {34},
      issn         = {0024-9297},
      address      = {Washington, DC},
      publisher    = {Soc.},
      reportid     = {PreJuSER-34172},
      pages        = {4907 - 4916},
      year         = {2001},
      note         = {Record converted from VDB: 12.11.2012},
      abstract     = {Blends of poly(styrene)-b-poly(isoprene) (PS-PI) and poly(
                      isoprene)-b-poly(ethylene oxide) (PI-PEO) were investigated
                      by small-angle X-ray scattering, photon correlation
                      spectroscopy, light microscopy, and rheology. Blends were
                      prepared in which both diblocks had the same PI composition,
                      f, and were investigated as a function of blend composition,
                      Phi. We generally found a disordered one-phase region at
                      high temperatures and two macrophase-separated, ordered
                      phases at low temperatures. At low temperatures the only
                      appreciable miscibility was found for f = 0.7 in the
                      PI-PEO-rich phase. At intermediate temperatures we generally
                      observed macrophase separation before microphase separation
                      upon cooling. The macrophase separation boundary compared to
                      the microphase boundary is lowered upon increasing f. For f
                      = 0.6 and 0.7 we observe an adjustment of the d spacing of
                      the macrophase-separated, ordered phases. The general trend
                      of the phase behavior is described by a theory using the
                      random phase approximation.},
      keywords     = {J (WoSType)},
      cin          = {IFF-NST},
      ddc          = {540},
      cid          = {I:(DE-Juel1)VDB34},
      pnm          = {Polymere, Membranen und komplexe Flüssigkeiten},
      pid          = {G:(DE-Juel1)FUEK53},
      shelfmark    = {Polymer Science},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:000169564100036},
      doi          = {10.1021/ma010233q},
      url          = {https://juser.fz-juelich.de/record/34172},
}