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Synthesis, Curing Behavior and Swell Tests of pH-Responsive Coatings from Acryl-Terminated Oligo(beta-Amino Esters)
Mid Sweden University, Sweden.
RISE - Research Institutes of Sweden, ICT, Acreo. Mid Sweden University, Sweden.ORCID-id: 0000-0002-0631-3804
Mid Sweden University, Sweden.
Mid Sweden University, Sweden.
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2018 (Engelska)Ingår i: Chemosensors, ISSN 2227-9040, Vol. 6, nr 1, artikel-id 10Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The ability of acryl-terminated oligo(beta-amino esters) (AOBAE) to be coated on fibers and printed electronics without solvents and to be cross-linked to a pH-responsive coatings, makes AOBAE-based coatings a potential type of pH-sensor coating. However, there are currently no reports of AOBAEs used as a pH-responsive coating material in sensor applications. Here we present an investigation of the synthesis, curing behavior and swell tests of AOBAEs. AOBAEs were synthesized from reacting an excess of asymmetric diacrylates with piperazine without the use of any solvents. They were then cross-linked to an insoluble network by UV-curing. Nuclear magnetic resonance (NMR) and Fourier transform infrared (FTIR) spectroscopy were used to characterize the AOBAEs. NMR was used to clarify the irregular structure of the AOBAE. FTIR was used to monitor the effects of UV-curing dose and air exposure on monomer conversion during curing. An interferometric technique was used to monitor the swelling behavior of the coating in response to pH variations. Swell experiments showed that the AOBAE also responded to pH variations after polymerization. Therefore, AOBAE is an interesting class of material with potential use as a pH responsive coating in optical-and printed electronics pH-sensors applications.

Ort, förlag, år, upplaga, sidor
MDPI , 2018. Vol. 6, nr 1, artikel-id 10
Nyckelord [en]
oligo(beta-amino esters); acryl-terminated; 1, 3-butanediol diacrylate; piperazine; pH; sensor; coating; thin film
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URN: urn:nbn:se:ri:diva-33641DOI: 10.3390/chemosensors6010010Scopus ID: 2-s2.0-85045393278OAI: oai:DiVA.org:ri-33641DiVA, id: diva2:1197822
Tillgänglig från: 2018-04-14 Skapad: 2018-04-14 Senast uppdaterad: 2023-05-25Bibliografiskt granskad

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