Affiliations 

  • 1 Department of Mechanical & Materials Engineering, Faculty of Engineering & Built Environment, University Kebangsaan Malaysia, Bangi, Selangor 43600, Malaysia. taysersumer@gmail.com
  • 2 Department of Chemical & Process Engineering, Faculty of Engineering & Built Environment, Universiti Kebangsaan Malaysia, Bangi, Selangor 43600, Malaysia. amir8@ukm.edu.my
  • 3 Department of Chemical & Process Engineering, Faculty of Engineering & Built Environment, Universiti Kebangsaan Malaysia, Bangi, Selangor 43600, Malaysia. caddy.tina@gmail.com
  • 4 Energy and Renewable Energies Technology Centre, University of Technology, Baghdad 10001, Iraq. dr.ahmed1975@gmail.com
  • 5 Department of Mechanical & Materials Engineering, Faculty of Engineering & Built Environment, University Kebangsaan Malaysia, Bangi, Selangor 43600, Malaysia. abubakar@ukm.edu.my
  • 6 Program of Chemical Engineering, Taylor's University-Lakeside Campus, Subang Jaya, Selangor 47500, Malaysia. mhnassir1949@gmail.com
  • 7 Solar Energy Research Institute (SERI), Universiti Kebangsaan Malaysia, Bangi, Selangor 43600, Malaysia. eng_tay83@yahoo.com
Polymers (Basel), 2017 Jun 06;9(6).
PMID: 30970887 DOI: 10.3390/polym9060207

Abstract

A halloysite nanotubes⁻polyvinyl alcohol⁻polyvinylpyrrolidone (HNTs⁻PVA⁻PVP) composite has been investigated for a quite long time aiming at improving the physico⁻chemical characterization of HNTs. In this work, HNTs⁻PVA⁻PVP composite were prepared based on a unique procedure characterized by crosslinking two polymers with HNTs. The composite of two polymers were modified by treating HNTs with phosphoric acid (H₃PO₄) and by using malonic acid (MA) as a crosslinker. The composite was also treated by adding the dispersion agent sodium dodecyl sulfate (SDS). The HNTs⁻PVA⁻PVP composite shows better characteristics regarding agglomeration when HNTs is treated in advance by H₃PO₄. Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM), brunauer⁻emmett⁻teller (BET), size distribution, and atomic force microscopy (AFM) are used to characterize the physio-chemical properties of the composite. FTIR shows additional peaks at 2924.29, 1455.7, and 682.4 cm-1 compared to the neat HNTs due to adding MA. Despite that, the XRD spectra do not show a significant difference, the decrease in peak intensity could be attributed to the addition of semi-crystalline PVA and the amorphous PVP. The images taken by TEM and FESEM show the possible effects of MA on the morphology and internal feature of HNTs⁻PVA⁻PVP composite treated by MA by showing the deformation of the matrix. The BET surface area increased to 121.1 m²/g compared to the neat HNTs at 59.1 m²/g. This result, the second highest recorded result, is considered a breakthrough in enhancing the properties of HNTs⁻PVA⁻PVP composite, and treatment by MA crosslinking may attribute to the size and the number of the pores. The results from these techniques clearly showed that a significant change has occurred for treated HNTs⁻PVA⁻PVP composite where MA was added. The characterization of HNTs⁻PVA⁻PVP composite with and without treating HNTs and using crosslinker may lead to a better understanding of this new composites as a precursor to possible applications in the dentistry field.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.