Crosslinked Poly Glycidyl Methacrylate Research Articles

Preparation and application of porous functional polymers for boron removal in seawater desalination by a mild and free-organic solvents process

The development of high-performance adsorbents to address high concentrations of boron and thus acquirement of drinkable water from seawater is a huge challenge. Most of the boron removal adsorbents reported in the literature have complex and organic solvents involved in preparation processes, which makes industrial production difficult. Herein, the porous cross-linked polyglycidyl methacrylate (CLPGMA) with a rich pore structure is prepared in one step by water-in-oil high internal phase emulsification, and then functionalized using water as a solvent to dissolve glucosamine to obtain the boron removal adsorbent. The whole preparation process is facile and free-organic solvents, making it suitable for further industrial production. The adsorbent demonstrates excellent performance in batch adsorption. Especially, we propose to combine the adsorption with reverse osmosis technology, by which the drinkable desalinated seawater can be obtained. The column adsorption experiments show that the adsorbent can rapidly remove boron from desalinated seawater at high flow rates under dynamic conditions to meet drinking water standards. This research provides a new method for the green large-scale synthesis of high-performance boron adsorbent for seawater desalination.

Preparation and evaluation of maltose modified polymer-silica composite based on cross-linked poly glycidyl methacrylate as high performance liquid chromatography stationary phase

A new maltose modified polymer-silica composite was fabricated and applied as high performance liquid chromatography (HPLC) stationary phase. The cross-linked poly glycidyl methacrylate (pGMA) layer was chemically bonded to the outer surface as well as pore inner surface of silica beads via in-situ polymerization, and then maltose was modified onto the polymer layer via a [3 + 2] “click” reaction. The porous spherical silica (4 μm diameter) with 300 Å pore size was selected as the matrix so that the 3.25 nm-thick polymer layer fabricated on the pore inner surface would not affect its permeability. The typical ‘U-shape’ retention curves indicated a mixed-mode retention mechanism of the as-synthesized stationary phase. Both polar and non-polar analytes could be well separated on the stationary phase with column efficiency reaching 123809 plates/m for guanosine in hydrophilic interaction liquid chromatography (HILIC) mode and 46808 plates/m for fluorene in reversed-phase liquid chromatography (RPLC) mode, respectively. Nucleotides and their bases were baseline separated with good peak shape without any buffer salt in mobile phase, suggesting the effective shielding of the silanol groups. The packing material also showed excellent chromatographic repeatability with intraday RSDs of the retention time of five nucleosides less than 0.048% (n = 3) and interday RSDs less than 0.33% (n = 7) and great pH stability (from 1.5 to 10.2). Finally, the stationary phase was applied to the separation of ginseng extract.