Dental Materials
Volume 25, Issue 3 , Pages 339-347, March 2009

PMMA-grafted nanoclay as novel filler for dental adhesives

  • Mohammad Atai

      Affiliations

    • Iran Polymer and Petrochemical Institute (IPPI), P.O. Box 14965/115, Tehran, Iran
    • Corresponding Author InformationCorresponding author. Tel.: +98 21 44580085; fax: +98 21 44580023.
  • ,
  • Laleh Solhi

      Affiliations

    • Iran Polymer and Petrochemical Institute (IPPI), P.O. Box 14965/115, Tehran, Iran
  • ,
  • Azizollah Nodehi

      Affiliations

    • Iran Polymer and Petrochemical Institute (IPPI), P.O. Box 14965/115, Tehran, Iran
  • ,
  • Seyed Mojtaba Mirabedini

      Affiliations

    • Iran Polymer and Petrochemical Institute (IPPI), P.O. Box 14965/115, Tehran, Iran
  • ,
  • Shahin Kasraei

      Affiliations

    • Dental Research Center, Hamadan University of Medical Sciences, Hamadan, Iran
  • ,
  • Khatereh Akbari

      Affiliations

    • Dental Research Center, Hamadan University of Medical Sciences, Hamadan, Iran
  • ,
  • Samal Babanzadeh

      Affiliations

    • Iran Polymer and Petrochemical Institute (IPPI), P.O. Box 14965/115, Tehran, Iran

Received 29 March 2008; received in revised form 8 July 2008; accepted 6 August 2008.

Abstract 

Objective

The aim of this study was to investigate the benefits of incorporation of poly(methyl methacrylate)-grafted-nanoclay on the bond strength of an experimental one-bottle dentin bonding system. The effect of the modification on the stability of the nanoparticle dispersion in the dilute adhesive was also studied.

Materials and methods

Poly(methyl methacrylate) was grafted onto the pristine Na-MMT nanoclay (Cloisite® Na+) through the free radical polymerization of methyl methacrylate in an aqueous media in the presence of ammonium persulfate as initiator. A reactive surfactant (AMPS) was also used in the reaction recipe to provide active sites on the surface of the nanoclay. The grafting polymerization reaction was carried out at 70°C. The PMMA-g-nanoclay was then coagulated in methanol and filtered. The resulting PMMA-g-nanoclay was characterized using FTIR, TGA, X-ray diffraction (XRD) and particle size distribution analysis. The modified nanoclay was added to an experimental dentin bonding system as filler and the morphology of the nanoclay layers in the adhesive matrix was studied using TEM and XRD. Shear bond strength of the adhesives containing different filler contents was tested on the caries-free extracted human premolar teeth. The mode of failure was studied by scanning electron microscopy. The stability of the nanoclay dispersion in the dilute adhesive was also studied using a separation analyzer. The results were then statistically analyzed and compared.

Results

The grafting of poly(methylmethacrylate) onto the nanoclay was confirmed and the results revealed a partially exfoliated structure for the PMMA-g-nanoclay. Incorporation of the modified nanoclay provided a dentin bonding system with higher shear bond strength. The dispersion stability of the modified nanoparticles in the dilute adhesive was also increased more than 40 times in comparison with the pristine nanoclay.

Significance

The grafting modification provided nanoclay particles with higher dispersion stability than pristine Na-MMT nanoclay in a dilute dentin bonding system. Incorporation of the modified nanoclay into the bonding system provided higher shear bond strength. The finding would be beneficial in producing nano-filler containing adhesive systems.

Keywords: Dental adhesives, Dentin bonding system, Nanoclay, Graft polymerization, Poly(methyl methacrylate) (PMMA)

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PII: S0109-5641(08)00214-5

doi:10.1016/j.dental.2008.08.005

Dental Materials
Volume 25, Issue 3 , Pages 339-347, March 2009