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Synthesis of PolyN-isopropylacrylamide Janus Microhydrogels for Anisotropic Thermo-responsiveness and Organophilic/Hydrophilic Loading Capability
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CO(2)-responsive polyacrylamide microspheres with interpenetrating networks.

Meng Mu1, Hongyao Yin2, Yujun Feng2

  • 1Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu 610041, PR China; University of Chinese Academy of Sciences, Beijing 100049, PR China.

Journal of Colloid and Interface Science
|March 13, 2017
PubMed
Summary
This summary is machine-generated.

Interpenetrating network (IPN) microspheres overcome agglomeration issues, offering enhanced CO2-responsiveness. These intelligent particles demonstrate reversible volume changes, enabling advanced applications.

Keywords:
CO(2)-responsivenessInterpenetrating networkInverse-suspension polymerizationMicrospheresPolyacrylamide

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Area of Science:

  • Materials Science
  • Polymer Chemistry
  • Nanotechnology

Background:

  • CO2-responsive microspheres are promising for various applications.
  • Particle agglomeration limits the utility of traditional co-polymerized microspheres.
  • Interpenetrating network (IPN) structures offer a potential solution to enhance microsphere stability and responsiveness.

Purpose of the Study:

  • To fabricate and characterize CO2-responsive polyacrylamide (PAM)/poly(dimethyl aminopropyl methacrylamide) (PDMAPMA) IPN microspheres.
  • To investigate the effect of DMAPMA loading and crosslinking degree on IPN microsphere structure and CO2-responsiveness.
  • To demonstrate the superiority of IPN structures over co-polymerization for preventing particle agglomeration.

Main Methods:

  • Fabrication of PAM/PDMAPMA IPN microspheres via inverse seed suspension polymerization.
  • Characterization using Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), optical microscopy (OM), and laser particle size analysis (LS).
  • Evaluation of CO2-responsiveness through alternating treatment with CO2 and N2 gases.

Main Results:

  • SEM confirmed homogeneous, compact IPN structures without phase separation.
  • Particle morphology transitioned from IPN to IPN-membrane with increasing DMAPMA concentration.
  • Microspheres exhibited reversible volume expansion and collapse upon CO2/N2 treatment.
  • Non-agglomerated particles were prepared by adjusting seed crosslinking degree.
  • Maximum relative swelling volume (RSV) reached 11.6 at 87% PDMAPMA loading.

Conclusions:

  • IPN protocol effectively prevents agglomeration in CO2-responsive microspheres.
  • The fabricated PAM/PDMAPMA IPN microspheres exhibit tunable CO2-responsiveness.
  • These non-agglomerated, intelligent microspheres show significant potential for advanced applications requiring controlled volume changes.