Synthesis and properties of the new difunctional methacrylate monomer 2‐hydroxy‐3‐methacryloyloxypropoxybenzene are presented. This monomer was applied for the synthesis of porous microspheres. It was copolymerized with trimethylolpropane trimethacrylate in the presence of two pairs of pore‐forming diluents dodecane and toluene, and n‐decanol and toluene. Influence of diluents composition on their porous structures was studied. Thermal resistance and tendency to swell in different organic diluents for a chosen sample were also determined. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 6165–6174, 2008

ABSTRACT:The new aromatic tetrafunctional methacrylate monomer, 1,4-di(2-hydroxy-3-methacryloyloxypropoxy) phenol, and its application for the synthesis of porous microspheres have been presented. It was copolymerized with trimethylolpropane trimethacrylate in the presence of pore-forming diluents mixture (chlorobenzene and 1-decanol). The results indicate that composition of diluents mixture influence porous structure of copolymers. The porous structure of the copolymer obtained in the presence of 50% chlorobenzene was studied in detail. The results show that pore volume and the most probable pore size diameters determined for the copolymer in the dry and in the wetted states are different.

Abstract. This paper presents the synthesis, physicochemical properties and modifications of 2-hydroxyethyl methacrylate copolymers. It describes the new 2-hydroxyethyl methacrylate hydrogels in the form of microbeads of different degrees of crosslinking (2, 5, 8, 10, 15 and 20% mol). As crosslinking monomers bis[4(2-hydroxy-3-methacryloyloxypropoxy) phenyl]-sulfide and ethylene glycol dimethacrylate were used. The new hydrogels were obtained by two alternative methods in a suspension copolymerisation procedure. The copolymers were modified with diethylenetriamine in an epoxide opening reaction. Thermal properties (differential scanning calorimetry, thermogravimetric analysis) and swelling characteristic in typical solvents of the obtained functional hydrogels were examined. The chemical structure of the copolymers before and after modification was confirmed by Fourier transform infrared spectroscopy and elemental analyses. Moreover, their sorptive properties in removal of Cu(II), Zn(II), Cd(II), and Pb(II) ions from aqueous solutions were also presented. The Langmuir and Freundlich isotherm models are used to describe the adsorption characteristics of the selected modified hydrogels.

A new aromatic, tetrafunctional methacrylate monomer, 4,4′‐di(2‐hydroxy‐3‐methacryloyloxypropoxy)benzophenone, and its application to the synthesis of porous microspheres are presented. This new monomer was copolymerized with divinylbenzene in the presence of pore‐forming diluents. The properties of the obtained highly crosslinked microspheres were investigated as column packing for high‐performance liquid chromatography. Their porous structures in both dry and wet states were studied and compared with those of poly(divinylbenzene) and the less crosslinked copolymer of 2,3‐epoxypropyl methacrylate and divinylbenzene. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 7014–7026, 2006

Synthesis of highly crosslinked methacrylate copolymers of in form of microspheres is presented. They are prepared from tetrafunctional methacrylate derivative of bis(4-hydroxyphenyl)sulfide, bis[4-(2-hydroxy-3-methacryloyloxypropoxy)phenyl]sulfide (BES-DM), and divinylbenzene (DVB). In chemical structure of these copolymers exhibit hydroxyl and ester groups of hydrophilic nature. Additionally, copolymer contains sulfur atoms coming from BES-DM monomer. Porous structure of the copolymers in the dry and wet state was studied.Microspheres possessing the largest pore volume and specific surface area were subjected to chromatographic investigations. The results show that polar functional groups existing in the chemical structure of the studied microspheres have influence on reversed-phase HPLC retention mechanism.