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Journal articles on the topic 'Glycidyl methacrylate and divinylbenzene copolymers'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Kuroda, H., and Z. Osawa. "Synthesis and characterization of macroporous glycidyl methacrylate-divinylbenzene copolymer beads." European Polymer Journal 31, no. 1 (1995): 57–62. http://dx.doi.org/10.1016/0014-3057(94)00126-x.

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2

Shuang, Chen Dong, Feng Yang, Yang Zhou, Peng Hui Li, and Ai Min Li. "Preparation and Characterization of Magnetic Strong-Base Anion Exchange Resin." Advanced Materials Research 239-242 (May 2011): 1838–41. http://dx.doi.org/10.4028/www.scientific.net/amr.239-242.1838.

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The magnetic copolymer was prepared by polymerization of glycidyl methacrylate (GMA) and divinylbenzene (DVB) in the presence of OA-modified magnetic nano-particles. The magnetic strong-base anion exchange resin (MAER) was formed by quaternization of magnetic copolymer. Transmission electron microscope (TEM) and scanning electron microscope (SEM) were used for observation of prepared magnetic nano-particle and MAER, respectively. FT-IR spectrometer was used to characterize the magnetic nano-particle and MAER. To explore the potential application of MAER for natural organic matter (NOM) removal

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3

Jelínková, Miroslava, Larisa K. Shataeva, Galina A. Tischenko, and František Švec. "Reactive polymers. 58. Polyampholytes based on macroporous copolymers of glycidyl methacrylate with ethylene glycol dimethacrylate or divinylbenzene." Reactive Polymers 11 (January 1989): 253–60. http://dx.doi.org/10.1016/0923-1137(89)90111-5.

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4

Pilař, J., D. Horák, J. Labský, and F. Švec. "E.p.r. study of spin-labelled glycidyl methacrylate-ethylene dimethacrylate and styrene-divinylbenzene suspension copolymers in the swollen state." Polymer 29, no. 3 (1988): 500–506. http://dx.doi.org/10.1016/0032-3861(88)90369-2.

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5

ZHU, Xiaoping, and Akinori JYO. "Column-mode Removal of Lead Ion with Macroreticular Glycidyl Methacrylate-divinylbenzene Copolymer-based Phosphoric Acid Resin." Journal of Ion Exchange 11, no. 3 (2000): 68–78. http://dx.doi.org/10.5182/jaie.11.68.

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6

NONAKA, Takamasa, Takayuki OHTSUKA, Yasuko UEMURA, and Seiji KURIHARA. "Preparation of the Resins Containing Phosphonium Residues from Glycidyl Methacrylate-1,4-Divinylbenzene Copolymer Beads and Antibacterial Activity of the Resins." NIPPON KAGAKU KAISHI, no. 7 (1995): 529–39. http://dx.doi.org/10.1246/nikkashi.1995.529.

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7

Yan, Xin, and Weihong Sun. "Synthesis and metal ion adsorption studies of chelating resins derived from macroporous glycidyl methacrylate-divinylbenzene copolymer beads anchored schiff bases." Journal of Applied Polymer Science 117, no. 2 (2010): 953–59. http://dx.doi.org/10.1002/app.31482.

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8

NONAKA, Takamasa, Yasuko UEMURA, and Seiji KURIHARA. "Preparation of the Resins Containing Quaternary Ammonium Groups from Glycidyl Methacrylate-1,4-Divinylbenzene Copolymer Beads and Antibacterial Activity of the Resins." NIPPON KAGAKU KAISHI, no. 12 (1994): 1097–106. http://dx.doi.org/10.1246/nikkashi.1994.1097.

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9

Wawrzkiewicz, Monika, Beata Podkościelna, and Przemysław Podkościelny. "Application of Functionalized DVB-co-GMA Polymeric Microspheres in the Enhanced Sorption Process of Hazardous Dyes from Dyeing Baths." Molecules 25, no. 22 (2020): 5247. http://dx.doi.org/10.3390/molecules25225247.

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Intensive development of many industries, including textile, paper, plastic or food, generate huge amounts of wastewaters containing not only toxic dyes but also harmful auxiliaries such as salts, acid, bases, surfactants, oxidants, heavy metal ions. The search for effective pollutant adsorbents is a huge challenge for scientists. Synthesis of divinylbenzene copolymer with glycidyl methacrylate functionalized with triethylenetetramine (DVB-co-GMA-TETA) resin was performed and the obtained microspheres were evaluated as a potential adsorbent for acid dye removal from dyeing effluents. The sorpt

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10

EGAWA, Hiroaki, Akinori JYO, and Chiu-Wen CHEN. "Studies on Selective Adsorption Resins. XXXV. Chelating Resins Containing Sulfur Donors Derived from Macroreticular Glycidyl Methacrylate-Divinylbenzene Copolymer Beads and Their Behavior in Adsorption and Elution of Au(III), Pd(II) and Pt(IV)." NIPPON KAGAKU KAISHI, no. 5 (1994): 442–49. http://dx.doi.org/10.1246/nikkashi.1994.442.

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11

Aprilita, Nurul Hidayat, Rania Bakry, Christian W. Huck, and Guenther K. Bonn. "POLY(GLYCIDYL METHACRYLATE-DIVINYLBENZENE) MONOLITHIC CAPILLARY AS A STATIONARY PHASE FOR THE REVERSED-PHASE CHROMATOGRAPHIC SEPARATION OF PROTEINS." Indonesian Journal of Chemistry 5, no. 1 (2010): 1–6. http://dx.doi.org/10.22146/ijc.21830.

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Capillary column with monolithic stationary phase was prepared from silanized fused-silica capillary of 200 µm I.D. by in situ free radical polymerization of divinylbenzene with glycidy methacrylate in the presence of decanol and tetrahydrofuran as porogens. The hydrodynamic and chromatographic properties of this monolith, such as backpressure at different flow-rate, pore size distribution, van Deemter plot and the effect of varying gradient-rate were investigated. Poly(glycidyl methacrylate-divinylbenzene) monolithic capillary has been used successfully for the reversed-phase chromatographic

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12

Aprilita, Nurul H., Christian W. Huck, Rania Bakry, et al. "Poly(Glycidyl Methacrylate/Divinylbenzene)-IDA-FeIIIin Phosphoproteomics." Journal of Proteome Research 4, no. 6 (2005): 2312–19. http://dx.doi.org/10.1021/pr050224m.

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13

Pu, Meng Lu, Wei Jiang, and Yue Qing Shen. "A Facile Method to Synthesize Responsive Magnetic Polymer Composite Nanoparticles with Multifunctional Groups." Advanced Materials Research 936 (June 2014): 734–39. http://dx.doi.org/10.4028/www.scientific.net/amr.936.734.

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Magnetite nanoparticles (MNPs) coated with poly (divinylbenzene-co-glycidyl methacrylate) particles (mPDGs) are prepared by co-polymerization of 1,4-divinylbenzene and glycidyl methacrylate monomers via batch emulsion polymerization. The Fe3O4nanoparticles modified by oleic acid are obtained by chemical precipitation. The chemical composition, morphology, magnetic content, magnetic properties and particle size of the composite particles are investigated using transmission electron microscopy, thermogravimetric analysis, vibrating sample magnetometer, and dynamic light scattering, respectively.

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14

Yadollahi, M., H. Bouhendi, M. J. Zohuriaan-Mehr, H. Farhadnejad, K. Kabiri, and S. M. Mirabedini. "Glycidyl Methacrylate Copolymers Modified with CO2." Soft Materials 11, no. 4 (2013): 430–39. http://dx.doi.org/10.1080/1539445x.2012.688783.

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15

Zhang, Minlian, and Yan Sun. "Poly(glycidyl methacrylate–divinylbenzene–triallylisocyanurate) continuous-bed protein chromatography." Journal of Chromatography A 912, no. 1 (2001): 31–38. http://dx.doi.org/10.1016/s0021-9673(01)00526-x.

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16

Piracha, Asifa, and Shagufta Zulfiqar. "The thermal degradation of glycidyl methacrylate-methyl methacrylate copolymers." Polymer Degradation and Stability 51, no. 1 (1996): 27–34. http://dx.doi.org/10.1016/0141-3910(95)00172-7.

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17

El-Hamouly, S. H., M. Z. Eisabee, and K. N. Abd El-Nour. "Dielectric behaviour of glycidyl methacrylatebutyl methacrylate copolymers." Journal of Materials Science 25, no. 2 (1990): 1251–54. http://dx.doi.org/10.1007/bf00585432.

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18

Zulfiqar, Mohammad, Asifa Paracha, and Shagufta Zulfiqar. "Thermal degradation of glycidyl methacrylate-styrene copolymers." Polymer Degradation and Stability 43, no. 3 (1994): 403–8. http://dx.doi.org/10.1016/0141-3910(94)90012-4.

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19

Iqbal, M. S., Yasmeen Jamil, T. Kausar, and M. Akhtar. "Thermal degradation study of glycidyl methacrylate acrylonitrile copolymers." Journal of Thermal Analysis and Calorimetry 96, no. 1 (2009): 225–33. http://dx.doi.org/10.1007/s10973-008-9009-z.

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20

Kudva, R. A., H. Keskkula, and D. R. Paul. "Compatibilization of nylon 6/ABS blendsusing glycidyl methacrylate/methyl methacrylate copolymers." Polymer 39, no. 12 (1998): 2447–60. http://dx.doi.org/10.1016/s0032-3861(97)00583-1.

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21

Gan, P. P., and D. R. Paul. "Blends of glycidyl methacrylate/methyl methacrylate copolymers with poly(vinylidene fluoride)." Journal of Polymer Science Part B: Polymer Physics 33, no. 11 (1995): 1693–703. http://dx.doi.org/10.1002/polb.1995.090331115.

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22

Balanovsky, N. V., and A. G. Cherednichenko. "Studies of aminolysis of acrylonitrile–divinylbenzene–methyl methacrylate copolymers." Moscow University Chemistry Bulletin 72, no. 1 (2017): 34–37. http://dx.doi.org/10.3103/s0027131417010035.

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23

Gohy, Jean-François, Sayed Antoun, and Robert Jérôme. "Self-aggregation of poly(methyl methacrylate)-block-poly(sulfonated glycidyl methacrylate) copolymers." Polymer 42, no. 21 (2001): 8637–45. http://dx.doi.org/10.1016/s0032-3861(01)00375-5.

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24

Basha, K. Anver, Thavikkannu Balakrishnan, Marcela Urzúa, et al. "Copolymers of Phenoxyethyl Methacrylate with Glycidyl Methacrylate: Synthesis, Characterization and Reactivity Ratios." International Journal of Polymeric Materials 57, no. 3 (2008): 216–27. http://dx.doi.org/10.1080/00914030701413306.

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25

Brar, A. S., and Kaushik Dutta. "Acrylonitrile and Glycidyl Methacrylate Copolymers: Nuclear Magnetic Resonance Characterization." Macromolecules 31, no. 15 (1998): 4695–702. http://dx.doi.org/10.1021/ma980184q.

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26

Gan, P. P., and D. R. Paul. "Interaction energies for blends based on glycidyl methacrylate copolymers." Polymer 35, no. 16 (1994): 3513–24. http://dx.doi.org/10.1016/0032-3861(94)90917-2.

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27

Limé, Fredrik, and Knut Irgum. "Preparation of Divinylbenzene and Divinylbenzene-co-Glycidyl Methacrylate Particles by Photoinitiated Precipitation Polymerization in Different Solvent Mixtures." Macromolecules 42, no. 13 (2009): 4436–42. http://dx.doi.org/10.1021/ma900150b.

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28

Mert, Emine Hilal, and Hüseyin Yıldırım. "Porous functional poly(unsaturated polyester-co-glycidyl methacrylate-co-divinylbenzene) polyHIPE beads through w/o/w multiple emulsions: preparation, characterization and application." e-Polymers 14, no. 1 (2014): 65–73. http://dx.doi.org/10.1515/epoly-2013-0071.

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AbstractPoly(unsaturated polyester-co-glycidyl methacrylate-co-divinylbenzene) poly high internal phase emulsion (HIPE) beads were synthesized via water-in-oil-in-water (w/o/w) multiple emulsions. HIPEs were prepared by using a commercial unsaturated polyester resin (UPR) and a mixture of glycidyl methacrylate (GMA) and divinylbenzene (DVB) as the cross-linker. The external surfactant was found to be a strong influence on the morphology of the beads. The porosity and the pore morphology of the resulting polyHIPE beads were investigated by scanning electron microscopy (SEM) and Brunauer-Emmett-

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29

Eom, Taejun, and Anzar Khan. "Selenonium Polyelectrolyte Synthesis through Post-Polymerization Modifications of Poly (Glycidyl Methacrylate) Scaffolds." Polymers 12, no. 11 (2020): 2685. http://dx.doi.org/10.3390/polym12112685.

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Atom transfer radical polymerization of glycidyl methacrylate monomer with poly(ethylene glycol)-based macroinitiators leads to the formation of reactive block copolymers. The epoxide side-chains of these polymers can be subjected to a regiospecific base-catalyzed nucleophilic ring-opening reaction with benzeneselenol under ambient conditions. The ß-hydroxy selenide linkages thus formed can be alkylated to access polyselenonium salts. 77Se-NMR indicates the formation of diastereomers upon alkylation. In such a manner, sequential post-polymerization modifications of poly(glycidyl methacrylate)

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30

Soykan, Cengiz, Misir Ahmedzade, and Mehmet Coşkun. "Copolymers of phenacyl methacrylate with glycidyl methacrylate: synthesis, characterization and monomer reactivity ratios." European Polymer Journal 36, no. 8 (2000): 1667–75. http://dx.doi.org/10.1016/s0014-3057(99)00230-x.

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31

Men’shikova, A. Yu, K. S. Inkin, T. G. Evseeva, et al. "Bioligand carriers based on methyl methacrylate copolymers with N-vinylformamide or glycidyl methacrylate." Colloid Journal 73, no. 1 (2011): 76–82. http://dx.doi.org/10.1134/s1061933x1101011x.

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32

Gunaydin, Okan, and Faruk Yilmaz. "Copolymers of Glycidyl Methacrylate with 3-Methylthienyl Methacrylate: Synthesis, Characterization and Reactivity Ratios." Polymer Journal 39, no. 6 (2007): 579–88. http://dx.doi.org/10.1295/polymj.pj2006180.

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33

Narasimhaswamy, T., S. C. Sumathi, and B. S. R. Reddy. "Phenyl methacrylate-glycidyl methacrylate copolymers: synthesis, characterization and reactivity ratios by spectroscopic methods." Polymer 32, no. 18 (1991): 3426–32. http://dx.doi.org/10.1016/0032-3861(91)90549-x.

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34

Baker, Erin Shammel, Jennifer Gidden, William J. Simonsick, Michael C. Grady, and Michael T. Bowers. "Sequence dependent conformations of glycidyl methacrylate/butyl methacrylate copolymers in the gas phase." International Journal of Mass Spectrometry 238, no. 3 (2004): 279–86. http://dx.doi.org/10.1016/j.ijms.2004.04.020.

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35

Rabelo, D., V. J. Silva, E. F. C. Alcântara, et al. "Fe2+and Fe3+adsorption on 2-vinylpyridine-divinylbenzene copolymers and acrylonitrile-methyl methacrylate-divinylbenzene terpolymers." Journal of Applied Polymer Science 89, no. 14 (2003): 3905–12. http://dx.doi.org/10.1002/app.12605.

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36

Park, Kang-Yeol, Won-Wook Jeong, and Kyung-Do Suh. "Monodisperse Crosslinked Microsphere Polymer Particles by Dispersion Copolymerization of Glycidyl Methacrylate and Divinylbenzene." Journal of Macromolecular Science, Part A 40, no. 6 (2003): 617–27. http://dx.doi.org/10.1081/ma-120020871.

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37

Kolyaganova, O. V., Sh Zh Aristangaliev, A. A. Rysukhina, et al. "WATER-REPELLENT PROPERTIES OF WOOD MODIFIED WITH GLYCIDYL METHACRYLATE COPOLYMERS." IZVESTIA VOLGOGRAD STATE TECHNICAL UNIVERSITY, no. 12(247) (December 24, 2020): 72–81. http://dx.doi.org/10.35211/1990-5297-2020-12-247-72-81.

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The paper considers the features of modification of wood (pine) with reactive copolymers based on glycidyl methacrylate and fluorine (alkyl) methacrylates to impart water-repellent properties. Such modification provides the achievement of superhydrophobic properties and a decrease in the water permeability of the material due to a smaller spot of contact of water drops with the surface. Wood water absorption index reduced by 3 times.

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38

Jovanovic, S. M., A. Nastasović, N. N. Jovanovic, and K. Jeremic. "Targeted Porous Structure of Macroporous Copolymers Based on Glycidyl Methacrylate." Materials Science Forum 214 (May 1996): 155–62. http://dx.doi.org/10.4028/www.scientific.net/msf.214.155.

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39

Zygadlo-Monikowska, Ewa, Zbigniew Florjanczyk, and Wladyslaw Wieczorek. "Polymer Gel Electrolytes Based on Glycidyl Methacrylate Homopolymer and Copolymers." Journal of Macromolecular Science, Part A 31, no. 9 (1994): 1121–34. http://dx.doi.org/10.1080/10601329408545710.

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40

Zygadło-Monikowska, Ewa, Zbigniew Florjańczyk, and Władysław Wieczorek. "Polymer Gel Electrolytes Based on Glycidyl Methacrylate Homopolymer and Copolymers." Journal of Macromolecular Science, Part A 31, no. 9 (1994): 1121–34. http://dx.doi.org/10.1080/10601329409351540.

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41

Brar, Ajaib Singh, and Anil Yadav. "Glycidyl Methacrylate and Vinylidene Chloride Copolymers. Nuclear Magnetic Resonance Characterisation." Polymer Journal 35, no. 1 (2003): 37–43. http://dx.doi.org/10.1295/polymj.35.37.

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42

Podkościelna, Beata. "Synthesis, modification, and porous properties of new glycidyl methacrylate copolymers." Journal of Applied Polymer Science 120, no. 5 (2011): 3020–26. http://dx.doi.org/10.1002/app.33420.

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43

Piracha, Asifa, Shagufta Zulfiqar, and I. C. McNeill. "The thermal degradation of copolymers of glycidyl methacrylate and vinylacetate." Polymer Degradation and Stability 51, no. 3 (1996): 319–26. http://dx.doi.org/10.1016/0141-3910(95)00202-2.

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44

Grigoreva, Alexandra O., Kseniia Tarankova, and Sergey D. Zaitsev. "Copolymerization of Glycidyl Methacrylate and 1,1,1,3,3,3-Hexafluoroisopropyl Acrylate." Key Engineering Materials 899 (September 8, 2021): 387–91. http://dx.doi.org/10.4028/www.scientific.net/kem.899.387.

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The copolymerization of 1,1,1,3,3,3-hexafluoroisopropyl acrylate (HFIPA) and glycidyl methacrylate via reversible addition-fragmentation chain transfer (RAFT) process was investigated. 2-cyano-2-propyl dodecyl trithiocarbonate (CPDT) was used as chain transfer agent. It is turned out that CPDT and polymeric chain transfer agent obtained based on HFIPA and CPDT provide a good control over molar mass characteristic of copolymers (Đ = 1.05). Reactivity ratios were found to be r1(GMA) = 1.57 and r2(HFIPA) = 0.05 by Fineman–Ross model.

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45

Markovic, Bojana, Vojislav Spasojevic, Aleksandra Dapcevic, et al. "Characterization of glycidyl methacrylate based magnetic nanocomposites." Chemical Industry 73, no. 1 (2019): 25–35. http://dx.doi.org/10.2298/hemind181113006m.

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Magnetic and non-magnetic macroporous crosslinked copolymers of glycidyl methacrylate and trimethylolpropane trimethacrylate were prepared by suspension copolymerization and functionalized with diethylenetriamine. The samples were characterized by mercury porosimetry, scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS), Fourier transform infrared spectroscopy analysis (FTIR-ATR), thermogravimetric analysis (TGA), X-ray diffractometry (XRD), atomic force microscopy (AFM), transmission electron microscopy (TEM) and SQUID magnetometry. The FTIR-ATR analysis of synthes

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46

Bryuzgin, Evgeny, Victor Klimov, Sergey Zaytsev, Alexander Navrotskiy, and Ivan Novakov. "Influence of the Structure of Glycidyl Methacrylate Copolymers on the Hydrophobic Properties of Cellulose Materials." Advanced Materials Research 1098 (April 2015): 98–103. http://dx.doi.org/10.4028/www.scientific.net/amr.1098.98.

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The modification of the surface of cellulose-containing materials by copolymers of polyglycidyl methacrylate (PGMA) obtained by means of two ways: acylation of PGMA by stearic acid and copolymerization of glycidyl methacrylate and lauryl methacrylate is proposed. It is demonstrated, that the use of obtained copolymers allows to get the superhydrophobic coatings on the surface of cellulose-containing materials with reaching of contact angles up to 161°. Such modified materials can be used as filters for the separation of the water-oil emulsions.

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47

Ratnaprabha, Khisti, and P. K. Daliya. "Functional copolymers ofp-cumyl phenyl methacrylate and glycidyl methacrylate: Synthesis, characterization, and reactivity ratios." Journal of Applied Polymer Science 97, no. 1 (2005): 336–47. http://dx.doi.org/10.1002/app.21732.

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48

Howe, David H., Ken J. Jenewein, James L. Hart, Mitra L. Taheri, and Andrew J. D. Magenau. "Functionalization-induced self-assembly under ambient conditions via thiol-epoxide “click” chemistry." Polymer Chemistry 11, no. 2 (2020): 298–303. http://dx.doi.org/10.1039/c9py01144g.

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Polymer micelles were formed using thiol-epoxide “click” chemistry to trigger functionalization-induced self-assembly (FISA) of block copolymers by modifying a reactive glycidyl methacrylate block with solvophobes.

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49

Sunaga, Keisuke, Min Kim, Kyoichi Saito, Kazuyuki Sugita, and Takanobu Sugo. "Characteristics of Porous Anion-Exchange Membranes Prepared by Cografting of Glycidyl Methacrylate with Divinylbenzene." Chemistry of Materials 11, no. 8 (1999): 1986–89. http://dx.doi.org/10.1021/cm980490i.

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50

Guo, Dandan, Chaoyan Lou, Peimin Zhang, et al. "Polystyrene-divinylbenzene-glycidyl methacrylate stationary phase grafted with poly (amidoamine) dendrimers for ion chromatography." Journal of Chromatography A 1456 (July 2016): 113–22. http://dx.doi.org/10.1016/j.chroma.2016.05.050.

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