ライフサイエンスコーパス: glycidyl methacrylate

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1 Affinity monoliths based on a copolymer of glycidyl methacrylate and ethylene dimethacrylate were d

2 These monoliths were based on a copolymer of glycidyl methacrylate and ethylene dimethacrylate.

3 red by direct in situ photopolymerization of glycidyl methacrylate and ethylene glycol dimethacrylate

4 crofluidic channel by photopolymerization of glycidyl methacrylate and trimethylolpropane trimethacry

5 ting frits by in situ photopolymerization of glycidyl methacrylate and trimethylolpropane trimethacry

6 the UV photopolymerization of a solution of glycidyl methacrylate and trimethylolpropane trimethacry

7 the UV photopolymerization of a solution of glycidyl methacrylate and trimethylopropane trimethacryl

8 l F diglycidyl ether (BFDGE) and Bisphenol A glycidyl methacrylate (BISGMA) after their exposure to l

9 The monomer mixture consisted of bisphenol A glycidyl methacrylate (BisGMA), hexanediol dimethacrylat

10 actor was fabricated in a fused silica using glycidyl methacrylate-co-ethylene dimethacrylate polymer

11 onolithic capillary prepared using GMA-EDMA (glycidyl methacrylate-co-ethylene dimethacrylate) as pol

12 ties of uniformly sized 3-microm porous poly(glycidyl methacrylate-co-ethylene dimethacrylate) beads

13 tionary phase obtained by hydrolysis of poly(glycidyl methacrylate-co-ethylene dimethacrylate) beads

14 The column is prepared from a poly(glycidyl methacrylate-co-ethylene dimethacrylate) monoli

15 These columns are prepared from a poly(glycidyl methacrylate-co-ethylene dimethacrylate) monoli

16 alities originating from the hydrolyzed poly(glycidyl methacrylate-co-ethylene dimethacrylate) monoli

17 ionalization of our affinity substrate, poly(glycidyl methacrylate-co-ethylene dimethacrylate) porous

18 ced a surface-reactive acrylic polymer, poly(glycidyl methacrylate-co-methyl methacrylate) (PGMAMMA),

19 A surface-reactive acrylic polymer, poly(glycidyl methacrylate-co-methyl methacrylate) (PGMAMMA),

20 ng a buffer ion-permeable membrane in a poly(glycidyl methacrylate-co-methyl methacrylate) micro elec

21 rticularly notable for a hydrophobic monomer glycidyl methacrylate combined with a nonionic surfactan

22 2-Hydroxyethyl methacrylate (HEMA) and glycidyl methacrylate (GMA) are examined to provide exce

23 An ethylenediamine functionalized glycidyl methacrylate (GMA) based terpolymeric chelating

24 ified sequentially with silica (Fe3O4@SiO2), glycidyl methacrylate (GMA) by surface initiated atom tr

25 Glycidyl methacrylate (GMA) was examined to provide exce

26 ylate (MMA) statistically copolymerized with glycidyl methacrylate (GMA), resulting in p(MMA-stat-GMA

27 ed carbon nanotube (MWCNT) was grafted using glycidyl methacrylate (GMA).

28 ion using La2O3, (ii) La2O3 embedded in poly(glycidyl methacrylate (GMA)/divinylbenzene (DVB)) tip, a

29 WNSYY was immobilized to the surface of poly(glycidyl methacrylate) nanoparticles (PGMA NPs).

30 ydroquinidine , ethylene dimethacrylate, and glycidyl methacrylate or 2-hydroxyethyl methacrylate in

31 ds were prepared by chemical modification of glycidyl methacrylate particles.

32 olymeric matrix composed of poly(ethylene-co-glycidyl methacrylate) (PEGM) has been prepared.

33 of a trimethacrylate monomer or bisphenol A glycidyl methacrylate, which is a monomer standard in de

34 rylate with the sodium salt of N-reaction of glycidyl methacrylate with the sodium salt of N-(3,5-dim

35 ) was synthesized by an addition reaction of glycidyl methacrylate with the sodium salt of N-reaction

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