Abstract

Herein we reported a novel method for preparation of hybrid molecularly imprinted polymer foams (MIPFs) via a twice imprinting strategy. Firstly, based on halloysite nanotubes (HNTs) cores, three molecularly imprinted nanomaterials (MIPs-S, MIPs-M and MIPs-L) with controlled thickness of imprinted shells (i.e., 7.0nm, 17nm and 36nm, respectively), were prepared by precipitation polymerization. The surface hydrophobicity of MIP nanomaterials gradually enhanced with the increasing thickness of imprinted shells. Secondly, three hybrid MIP foams (MIPFs-S, MIPFs-M, MIPFs-L) were successively fabricated by W/O Pickering high internal phase emulsions (HIPEs) template stabilized by the corresponding MIPs nanomaterials. Due to the increased hydrophobicity of the MIPs nanomaterials, the amount of interconnecting pores in hybrid MIPFs was continuously decreased until a closed-cell structure appeared, while the average void diameter increased from 10μm to 28μm. Binding experiments demonstrated that optimized hybrid MIP foams (MIPFs-M) possessed enhanced adsorption capacity, fast kinetics and excellent recognition ability towards λ-cyhalothrin (LC). Therefore, this two-step imprinting strategy could not only figure out the difficulty in solid–liquid phase separation and the recycling of nano-sized MIPs but also overcome the disadvantage of stabilizing solid particles on the surface of MIPFs referring to the lack of specific adsorption activity.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.