Free-radical copolymerization of cyclohexyl methacrylate (CHMA) and tetra (ethylene glycol) dimethacrylate (TtEGDMA) were carried out at 60 °C in tetrahydrofuran solution in presence of 2,2-azobisisobutyronitrile. The random copolymers were prepared with nominal crosslinking ratios, X of 1, 5 and 10% mol TtEGDMA / mol CHMA. The copolymers were characterized by 13C NMR spectroscopy. The copolymers was characterized by 13C RMN analysis and determined the copolymers composition. The monomer reactivity ratios r1 (TtEGDMA) and r2 (CHMA) were determined with the linearized copolymerization equations of the Fineman–Ross methods (r1 = 1.77 and r2 = 0.48) and Kelen–Tüdös (r1 = 1.81 and r2 = 0.46). Parameters of Alfrey-Price Q1 = - 1.10 (specific activity) and e1= - 0.64 (polarity) for TtEGDMA.

A BisGMA, TEGDMA monomer mixture at weight ration 2:1 was UV-cured with CQ to form commonly used dental materials. Three types of fillers at different particle size were added at different weight concentrations. Reaction rates k, time vs rate were studied for all the systems.

A series of commercial dental composites curable by visible light have been investigated and compared in terms of their photoreactivity thanks to the photocalorimetry technique by using two different types of lamps, a conventional lamp (halogen lamp) from ESPE and a plasma lamp, Apollo 98 E manufactured by DMDS. In terms of kinetics, dental composites cure in just a few seconds with plasma lamp compared to 20-40 s with halogen lamp allowing dentists to save time. Recent investigations on new composite systems having low contraction show that they are less photoreactive compared to former systems.

Besides others, textile industries are the primary sources of discharging a massive amount of highly colored wastewater. Adsorption can be considered the most economically favorable technology method for removing dyes from wastewater. This paper reports the synthesis of Poly tetra (ethyleneglycol) dimethacrylate crosslinked with 2-hydroxypropyl methacrylate (Poly (TtEGDMA-cross-2-HPMA)) hydrogelsand its application as a novel sorbent to remove bemacid red (ET2) dye from aqueous solution under various operating conditions. The equilibrium adsorption capacity was found 142.82–883.60 mg ET2 g–1 of 1% TtEGDMA. The adsorbent was characterized using Fourier transform infrared radiation (FTIR) and 13carbon solid-state nuclear magnetic resonance spectra (13C-NMR). The effects of the experimental parameters include dye concentration and crosslinked agent concentration. The kinetic sorption uptake for ET2 by Poly (TtEGDMA-cross-2-HPMA) at various initial dye concentrations was analyzed by pseudo-first and pseudo-second models. Two sorption isotherms, namely the Langmuir and Freundlich isotherms, were applied to the sorption equilibrium data. The sorption kinetics of ET2 onto the hydrogels followed the pseudo-second-order kinetics model (R2 = 0.999) and the adsorption equilibrium data obeyed the Langmuir isotherm model (R2 = 0.999). It can be concluded that Poly (TtEGDMA-cross-2-HPMA) is an alternative economic sorbent to more costly adsorbents used for dye removal in wastewater treatment processes.