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Sökning: AMNE:(NATURAL SCIENCES Chemical Sciences Polymer Chemistry) > Surface-confined ph...

Surface-confined photopolymerization of pH-responsive acrylamide/acrylate brushes on polymer thin films

Dunér, Gunnar (författare)
KTH,Kemi,Department of Chemistry, KTH
Anderson, Henrik (författare)
Uppsala universitet,Fasta tillståndets elektronik,Thin Films Group
Myrskog, Annica, 1980- (författare)
Linköpings universitet,Tekniska högskolan,Sensorvetenskap och Molekylfysik
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Hedlund, Maria (författare)
Uppsala universitet,Institutionen för fysik och materialvetenskap
Aastrup, Teodor (författare)
KTH,Kemi,Attana AB
Ramström, Olof (författare)
KTH,Organisk kemi,Department of Chemistry, KTH
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 (creator_code:org_t)
2008-06-19
2008
Engelska.
Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 24:14, s. 7559-7564
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Dynamic acrylamide/acrylate polymeric brushes were synthesized at gold-plated quartz crystal surfaces. The crystals were initially coated with polystyrene-type thin films, derivatized with photolabile iniferter groups, and subsequently subjected to photoinitiated polymerization in acrylamide/acrylate monomer feeds. This surface-confined polymerization method enabled direct photocontrol over the polymerization, as followed by increased frequency responses of the crystal oscillations in a quartz crystal microbalance (QCM). The produced polymer layers were also found to be highly sensitive to external acid/base stimuli. Large oscillation frequency shifts were detected when the brushes were exposed to buffer solutions of different pH. The dynamic behavior of the resulting polymeric brushes was evaluated, and the extent of expansion and contraction of the films was monitored by the QCM setup in situ in real time. The resulting responses were rapid, and the effects were fully reversible. Low pH resulted in full contractions of the films, whereas higher pH yielded maximal expansion in order to minimize repulsion around the charged acrylate centers. The surfaces also proved to be very robust because the responsiveness was reproducible over many cycles of repeated expansion and contraction. Using ellipsometry, copolymer layers were estimated to be similar to 220 nm in a collapsed state and similar to 340 nm in the expanded state, effectively increasing the thickness of the film by 55%.

Ämnesord

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)
NATURVETENSKAP  -- Kemi -- Polymerkemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Polymer Chemistry (hsv//eng)
NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)

Nyckelord

Bioelectric phenomena
Brushes
Chemical reactions
Crystallography
Frequency response
Gold
Molecular beam epitaxy
Monomers
Oxide minerals
Photopolymerization
Polyethylenes
Polymerization
Polymers
Powders
Quartz
Quartz crystal microbalances
Shrinkage
Thick films
Thin films
Chemistry
Kemi
Polymer chemistry
Surface and colloid chemistry
Ytbioteknik
NATURAL SCIENCES

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