A Novel Green Synthesis Method of Poly (3-Glycidoxypropyltrimethoxysilane) Catalyzed by Treated Bentonite

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 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Hydrogel composite of poly(vinylalcool) with unmodified montmorillonite

Crosslinked poly(vinylalcohol) (PVA) hydrogel composites based on algerian hydrophilic natural Na-montmorillonite (Na-MMT) nanoclay named Maghnite-Na (Mag-Na) were prepared in aqueous media, without utilization of chemical crosslinking agents, by repeated cycles of freezing and thawing. The morphology of hydrogel composites and their swelling in water at different amount of Mag-Na were investigated. The characterization of obtained hydrogel composites by X-ray diffraction (XRD) showed a remarkable increase of the basal distance of Mag-Na in PVA hydrogels. Therefore, Intercalated and exfoliated morphology was observed for prepared composites hydrogels of PVA. The infra-red (FTIR) characterization results showed that some interactions have been developed between the hydroxyl groups of PVA chains and Mag-Na in composite hydrogels. Introducing Mag-Na into PVA hydrogel affected their swelling. Increased amount of Mag-Na decreased the equilibrium degree of swelling and equilibrium water content

New approach for synthesis of poly(ethylglyoxylate) using Maghnite-H + , an Algerian proton exchanged montmorillonite clay, as an eco-catalyst

International audienceIn this works, we have explored a new method for a green synthesis of poly(ethylglyoxylate) (PEtG). This method consists on using a montmorillonite clay called Maghnite-H+ as an eco-catalyst to replace triethylamine which is toxic. Cationic polymerization experiments are performed in bulk conditions at three temperatures (-40 degrees C, 25 degrees C, 80 degrees C) and in THF solutions at room temperature (25 degrees C). At 25 degrees C, an optimum ratio of 5 wt% of catalyst leads to molar masses up to 22000 g/mol in THF solutions. Polymerizations in bulk conditions lead to slightly lower masses than experiments conducted in THF solutions. However, bulk polymerization of ethyleglyoxylate remains a preferable method in order to avoid the use of a solvent and therefore to stay in the context of green chemistry. The structure of obtained polymers are characterized and confirmed by H-1 and C-13 NMR. Thermogravimetric Analysis (TGA) shows an enhanced thermal stability for end-capped PEtG compared to non-terminated PEtG. The best conversion rate (92%) is observed in bulk conditions at 25 degrees C for a reaction time of 48h. An activation energy could be calculated from bulk experiments (Ea = 6.9kJ/mol). An interesting advantage of Maghnite-H+ is an easy recoverage by a simple filtration from the polymer solution