The present work focuses on the preparation and characterization of poly(3-Glycidoxypropyltrimethoxysilane) (PGPTMS) under mild conditions. Ring-opening polymerization of the 3-Glycidoxypropyltrimethoxysilane (GPTMS) is initiated with the bentonite of Maghnite-H+ (Mag-H+), an ecologic and low-cost catalyst. The evolution of epoxy ring-opening was studied in bulk and in solution using CH2Cl2 as solvent, as well as the influences of several factors such as the amount of Mag-H+, polymerization time and temperature on the yield of polymer were investigated. The best polymer yield (30 %) was obtained in bulk polymerization at room temperature (20 °C) for a reaction time 8 h, and it’s increases with time and reaches 68 % for 7 days. The structures of the obtained polymers (PGPTMS) were confirmed respectively by Fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance (NMR). The thermal properties of the prepared polymers were given by Differential Scanning Calorimetry (DSC) and thermogravimetric analysis (TGA), the Tg of PGPTMS is recorded at -31.27 °C, and it is thermally stable with a degradation start temperature greater than 300 °C, all  decomposition stopped at 600 °C. Copyright © 2020 BCREC Group. All rights reserved

Nanocomposites of linear poly(3-glycidoxypropyltrimethoxysilane) based on Algerian natural organophilic clay: montmorillonite–cetyltrimethylammonium named Maghnite-CTA were prepared by enhancing the dispersion of the matrix polymer in sheets of the organoclay. The effect of the organoclay, used with different amounts (3, 5, and 7% by weight) and the preparation method were studied in order to determine and evaluate their structural, morphological and thermal properties. X-ray diffraction analysis of obtained nanocomposites showed a significant change in the distance interlayer of montmorillonite–cetyltrimethylammonium. Therefore, interlayer expansion and exfoliation of linear poly(3-glycidoxypropyltrimethoxysilane) between layers of montmorillonite–cetyltrimethylammonium were observed. The thermal properties of the prepared nanocomposites were given by thermogravimetric analysis. The structure and morphology of the obtained materials were determined respectively by Fourier transform infrared spectroscopy and scanning electronic microscopy. The results obtained have approved the privilege of the intercalation of linear poly(3-glycidoxypropyltrimethoxysilane) in the interface of montmorillonite–cetyltrimethylammonium and the best quantity of organoclay required to prepare nanocomposite with a high thermal stability is 5% (by weight).

Telechelic poly(3-glycidoxypropyltrimetho¬xysilane) (PGPTMS) with acetate and methacrylate end groups was successfully synthesized by an efficient and solvent-free approach, with anhydrides (acetic anhydride (AA) and methacrylic anhydride (MA)), by cationic ring-opening polymerization of 3 glycidoxypropyl¬trimetho-xysilane (GPTMS), using an ecologic solid catalyst Maghnite-H+ (Mag-H+), instead of electrophilic catalysts, such as, Bronsted and Lewis acids which are very noxious and corrosive. Mag-H+ is a montmorillonite sheet silicate clay exchanged with protons. The structure of the obta¬ined macromonomers was confirmed by Fourier transform infrared spectroscopy (FT-IR), nuclear magnetic reso¬nance (NMR) and UV-visible spectroscopy. The presence of the methacrylate end groups of bis-macromonomers was determined by UV-visible spectroscopy. In order to find the optimal reaction conditions, effects of reaction time and the amount of anhydrides (AA and MA) on the yield of macromonomers were investigated.