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Modification of cel...
Modification of cellulose model surfaces by cationic polymer latexes prepared by RAFT-mediated surfactant-free emulsion polymerization
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- Carlsson, Linn (författare)
- KTH,Fiber- och polymerteknologi,Wallenberg Wood Science Center
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- Fall, Andreas (författare)
- KTH,Fiber- och polymerteknologi,Wallenberg Wood Science Center,KTH Royal Institute of Technology, Sweden
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Chaduc, I. (författare)
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- Wågberg, Lars (författare)
- KTH,Fiber- och polymerteknologi,Wallenberg Wood Science Center
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Charleux, B. (författare)
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- Malmström, Eva (författare)
- KTH,Fiber- och polymerteknologi
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D’Agosto, F. (författare)
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Lansalot, M. (författare)
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- Carlmark, Anna (författare)
- KTH,Fiber- och polymerteknologi
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(creator_code:org_t)
- 2014-06-30
- 2014
- Engelska.
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Ingår i: Polymer Chemistry. - : Royal Society of Chemistry. - 1759-9954 .- 1759-9962. ; 5:20, s. 6076-6086
- Relaterad länk:
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https://pubs.rsc.org...
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https://urn.kb.se/re...
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https://doi.org/10.1...
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https://urn.kb.se/re...
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Abstract
Ämnesord
Stäng
- This paper presents the successful surface modification of a model cellulose substrate by the preparation and subsequent physical adsorption of cationic polymer latexes. The first part of the work introduces novel charged polymer nanoparticles constituted of amphiphilic block copolymers based on cationic poly(N,N-dimethylaminoethyl methacrylate-co-methacrylic acid) (P(DMAEMA-co-MAA)) as the hydrophilic segment, and poly(methyl methacrylate) (PMMA) as the hydrophobic segment. First, RAFT polymerization of N,N-dimethylaminoethyl methacrylate (DMAEMA) in water was performed at pH 7, below its pKa. The simultaneous hydrolysis of DMAEMA led to the formation of a statistical copolymer incorporating mainly protonated DMAEMA units and some deprotonated methacrylic acid units at pH 7. The following step was the RAFT-mediated surfactant-free emulsion polymerization of methyl methacrylate (MMA) using P(DMAEMA-co-MAA) as a hydrophilic macromolecular RAFT agent. During the synthesis, the formed amphiphilic block copolymers self-assembled into cationic latex nanoparticles by polymerization-induced self-assembly (PISA). The nanoparticles were found to increase in size with increasing molar mass of the hydrophobic block. The cationic latexes were subsequently adsorbed to cellulose model surfaces in a quartz crystal microbalance equipment with dissipation (QCM-D). The adsorbed amount, in mg m-2, increased with increasing size of the nanoparticles. This approach allows for physical surface modification of cellulose, utilizing a water suspension of particles for which both the surface chemistry and the surface structure can be altered in a well-defined way.
Ämnesord
- TEKNIK OCH TEKNOLOGIER -- Materialteknik (hsv//swe)
- ENGINEERING AND TECHNOLOGY -- Materials Engineering (hsv//eng)
- NATURVETENSKAP -- Kemi -- Polymerkemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Polymer Chemistry (hsv//eng)
Nyckelord
- Acrylic monomers; Block copolymers; Cationic polymerization; Cellulose; Emulsification; Emulsion polymerization; Esters; Hydrophilicity; Hydrophobicity; Living polymerization; Nanoparticles; Polyacrylates; Polymers; Polymethyl methacrylates; Quartz; Quartz crystal microbalances; Self assembly; Surface active agents; Surface chemistry; Suspensions (fluids); Synthesis (chemical)
- Amphiphilic block copolymers; Cellulose model surfaces; Macromolecular raft agents; N
- N-dimethylaminoethyl methacrylate; Physical surface modifications; Poly(methyl methacrylate) (PMMA); Statistical copolymers; Surfactant-free emulsion polymerization
- Latexes
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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