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Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/22593

Title: Semipermeable elastic microcapsules for gas capture and sensing
Authors: Nabavi, Seyed Ali
Vladisavljevic, Goran T.
Gu, Sai
Manovic, Vasilije
Keywords: Elastic microcapsules
Glass capillary microfluidics
Semipermeable shell membrane
On-the-fly photopolymerisation
CO2 capture
Osmotic imbalance
Capillary-induced cavitation
Issue Date: 2016
Publisher: © American Chemical Society
Citation: NABAVI, S.A., 2016. Semipermeable elastic microcapsules for gas capture and sensing. Langmuir, 32(38), pp 9826–9835.
Abstract: Monodispersed microcapsules for gas capture and sensing were developed consisting of elastic semipermeable polymer shells of tuneable size and thickness and pH-sensitive, gas selective liquid cores. The microcapsules were produced using glass capillary microfluidics and continuous on-the-fly photopolymerisation. The inner fluid was 5-30 wt% K2CO3 solution with m-cresol purple, the middle fluid was a UV-curable liquid silicon rubber containing 0-2 wt% Dow Corning® 749 fluid, and the outer fluid was aqueous solution containing 60-70 wt% glycerol and 0.5-2 wt% stabiliser (polyvinyl alcohol, Tween 20 or Pluronic® F-127). An analytical model was developed and validated for prediction of the morphology of the capsules under osmotic stress based on the shell properties and the osmolarity of the storage and core solutions. The minimum energy density and UV light irradiance needed to achieve complete shell polymerisation were 2 J∙cm-2 and 13.8 mW·cm-2, respectively. After UV exposure, the curing time for capsules containing 0.5 wt% Dow Corning® 749 fluid in the middle phase was 30-40 min. The CO2 capture capacity of 30 wt% K2CO3 capsules was 1.6-2 mmol/g depending on the capsule size and shell thickness. A cavitation bubble was observed in the core when the internal water was abruptly removed by capillary suction, whereas a gradual evaporation of internal water led to buckling of the shell. The shell was characterised using TGA, DSC, and FTIR. The shell degradation temperature was 450-460°C.
Description: The videos accompanying the paper are contained beneath the publishers URL. This paper is in closed access until 3rd September 2017.
Sponsor: This work received financial support from the EPSRC grant EP/HO29923/1.
Version: Accepted for publication
DOI: 10.1021/acs.langmuir.6b02420
URI: https://dspace.lboro.ac.uk/2134/22593
Publisher Link: http://dx.doi.org/10.1021/acs.langmuir.6b02420
ISSN: 1520-5827
Appears in Collections:Closed Access (Chemical Engineering)

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