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Journal articles on the topic 'Ether(methyl vinyl)polymère'

Author: Grafiati

Published: 19 September 2021

Last updated: 30 July 2025

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1

Prodaevich, V., N. Valetova, A. Mitin, and L. Semenycheva. "Synthesis of pectin-based graft copolymers with synthetic fragments of vinyl monomers using the triethylborane-oxygen initiating system." Bulletin of the South Ural State University series "Chemistry" 15, no. 2 (2023): 90–99. http://dx.doi.org/10.14529/chem230208.

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The study of trialkylborane as a component of the initiating system with oxygen was carried out using the example of graft polymerization of alkyl(meth)acrylate vinyl butyl ether copolymer units on pectin polysaccharide. The amine complex triethylborane-hexamethylenediamine was introduced into a boiling mixture of an aqueous solution of pectin in vinyl butyl ether, after which a solution of the active monomer, alkyl(meth)acrylate, containing methacrylic acid, was introduced by the compensation method to isolate triethylborane from the complex. As a result of synthesis from a mixture containing

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2

Kuang, Chen, Sahar Qavi, and Reza Foudazi. "Double-stage phase separation in dynamically asymmetric ternary polymer blends." RSC Advances 6, no. 94 (2016): 92104–14. http://dx.doi.org/10.1039/c6ra17274a.

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In this work, the phase separation behavior of ternary blends of polystyrene/poly(vinyl methyl ether)/polyisoprene, PS/PVME/PI, and polystyrene/poly(vinyl methyl ether)/poly(ethyl methacrylate), PS/PVME/PEMA are investigated.

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3

Verma, A., A. Nielsen, J. E. Mcgrath, and J. S. Riffle. "Synthesis of a Model Triblock for Novel Thermoplastic Elastomers." Rubber Chemistry and Technology 64, no. 4 (1991): 601–9. http://dx.doi.org/10.5254/1.3538575.

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Abstract Thus far, we have been successful in preparing novel diblock and triblock copolymers comprised of poly(methyl methacrylate) and poly(butyl vinyl ether). Future work will focus on studying the morphology of both the diblock and triblock copolymers. Moreover, we are also interested in synthesizing triblocks with long poly(butyl vinyl ether) segments and short PMMA segments, since these polymers have the potential for exhibiting good elastomeric properties.

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4

Lievens, Serge S., and Eric J. Goethals. "Poly(methyl vinyl ether-b-octadecyl vinyl ether): a New Non-ionic Surfactant." Polymer International 41, no. 4 (1996): 437–41. http://dx.doi.org/10.1002/(sici)1097-0126(199612)41:4<437::aid-pi634>3.0.co;2-5.

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5

Qu, Chengke, Zhenhua Li, and Junpo He. "Synthesis of copolymers with an exact alternating sequence using the cationic polymerization of pre-sequenced monomers." Polymer Chemistry 9, no. 25 (2018): 3455–60. http://dx.doi.org/10.1039/c8py00626a.

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6

Willet, Nicolas, Sabine Gabriel, Christine Jérôme, Filip E. Du Prez, and Anne-Sophie Duwez. "Collapsing and reswelling kinetics of thermoresponsive polymers on surfaces: a matter of confinement and constraints." Soft Matter 10, no. 37 (2014): 7256–61. http://dx.doi.org/10.1039/c4sm01266f.

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7

Chesnokova, Alexandra N., Oksana V. Lebedeva, Yury N. Pozhidaev, Nikolay A. Ivanov, and Alexander E. Rzhechitskii. "Synthesis and Properties of Composite Membranes for Polymer Electrolyte Membrane Fuel Cells." Advanced Materials Research 884-885 (January 2014): 251–56. http://dx.doi.org/10.4028/www.scientific.net/amr.884-885.251.

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The paper is devoted to the sol-gel synthesis of proton conductive organic-silicon composite membranes based on tetraethyl orthosilicate (TEOS) and copolymers of 2-methyl-5-vinylpyridine and vinyl chloride (MVP-VC), 2-methyl-5-vinylpyridine and vinyl acetate (MVP-VA), copolymers of ethylene glycol vinyl glycidyl ether and styrene (KS-1 and KS-2), and nitrogen-containing heteroaromatic derivatives of sulfonic acids: 2-phenyl-5-benzimidazolsulfonic acid (PBISA) and pyridine-3-sulfonic acid (PSA). Properties of synthesized membranes, such as proton conductivity, activation energy, ion exchange ca

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8

Markova, M. V., I. V. Tatarinova, K. А. Apartsin, V. V. Kireeva, and B. A. Trofimov. "Cationic copolymerization of cholesterol vinyl ether with methylvinylsulfide: toward medicinal polymers." Доклады Академии наук 489, no. 5 (2019): 473–77. http://dx.doi.org/10.31857/s0869-56524895473-477.

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Oligomers of cholesterol vinyl ether (CVE) with methyl vinyl sulfide synthesized in the presence of cationic catalyst ВF3 OEt2 in up to 81% yield (Mn up to 5700) demonstrate optical activity exceeding that of CVE homopolymer, which is probably due to both conformational effects of the oligomer chain and chirality induction during the polymerization.

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9

Takahashi, Yoshiaki, Hirokazu Suzuki, Yoshiki Nakagawa, Masayoshi Yamaguchi, and Ichiro Noda. "Viscoelastic Properties of Poly(vinyl methyl ether)." Polymer Journal 23, no. 11 (1991): 1333–37. http://dx.doi.org/10.1295/polymj.23.1333.

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10

Pyda, M., K. Van Durme, B. Wunderlich, and B. Van Mele. "Heat capacity of poly(vinyl methyl ether)." Journal of Polymer Science Part B: Polymer Physics 43, no. 16 (2005): 2141–53. http://dx.doi.org/10.1002/polb.20504.

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11

Confortini, Ondine, and Filip E. Du Prez. "Functionalized Thermo-Responsive Poly(vinyl ether) by Living Cationic Random Copolymerization of Methyl Vinyl Ether and 2-Chloroethyl Vinyl Ether." Macromolecular Chemistry and Physics 208, no. 17 (2007): 1871–82. http://dx.doi.org/10.1002/macp.200700205.

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12

Koyama, Yasuhito, Takahiro Yoshii, Yasuhiro Kohsaka, and Toshikazu Takata. "Photodegradable cross-linked polymer derived from a vinylic rotaxane cross-linker possessing aromatic disulfide axle." Pure and Applied Chemistry 85, no. 4 (2013): 835–42. http://dx.doi.org/10.1351/pac-con-12-08-14.

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A new concept for photodegradable cross-linked polymers utilizing characteristics of rotaxane cross-links and aromatic disulfides is proposed. The cross-linked polymer is obtained by the radical polymerization of a vinyl monomer in the presence of a [3]rotaxane-type cross-linker having two radically polymerizable groups. The [3]rotaxane-type cross-linker was prepared in 93 % yield by the typical rotaxane-forming reaction using a dumbbell-shaped aromatic disulfide possessing a bis(ammonium salt) moiety and a crown ether wheel tethered by a hydroxymethyl group (96 %) and the subsequent vinyl gro

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13

Jabbari, Esmaiel, and Nikolaos A. Peppas. "Comparison of interdiffusion at polystyrene–poly(vinyl methyl ether) and polystyrene–poly(isobutyl vinyl ether) interfaces." Polymer International 38, no. 1 (1995): 65–69. http://dx.doi.org/10.1002/pi.1995.210380108.

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14

Verdonck, Beatrice, Eric J. Goethals, and Filip E. Du Prez. "Block Copolymers of Methyl Vinyl Ether and Isobutyl Vinyl Ether With Thermo-Adjustable Amphiphilic Properties." Macromolecular Chemistry and Physics 204, no. 17 (2003): 2090–98. http://dx.doi.org/10.1002/macp.200350069.

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15

Green, Peter F., Douglas B. Adolf, and Laura R. Gilliom. "Dynamics of polystyrene/poly(vinyl methyl ether) blends." Macromolecules 24, no. 11 (1991): 3377–82. http://dx.doi.org/10.1021/ma00011a052.

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16

Reyntjens, Wouter G., Laura Jonckheere, and Eric J. Goethals. "Thermotropic Networks Based on Poly(Methyl Vinyl Ether)." Journal of Macromolecular Science, Part A 40, no. 1 (2003): 1–10. http://dx.doi.org/10.1081/ma-120016669.

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17

Theiss, Daniel, Thomas Schmidt, and Karl-Friedrich Arndt. "Temperature-sensitive poly(vinyl methyl ether) hydrogel beads." Macromolecular Symposia 210, no. 1 (2004): 465–74. http://dx.doi.org/10.1002/masy.200450652.

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18

Theiss, Daniel, Thomas Schmidt, Helmut Dorschner, Rudolf Reichelt, and Karl-Friedrich Arndt. "Filled temperature-sensitive poly(vinyl methyl ether) hydrogels." Journal of Applied Polymer Science 98, no. 5 (2005): 2253–65. http://dx.doi.org/10.1002/app.22015.

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19

Coelho, Janaina Moreira, Nichollas Serafim Camargo, Rayane Ganassin, et al. "Oily core/amphiphilic polymer shell nanocapsules change the intracellular fate of doxorubicin in breast cancer cells." Journal of Materials Chemistry B 7, no. 41 (2019): 6390–98. http://dx.doi.org/10.1039/c9tb00587k.

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The aim of this work was to develop and test the in vitro biological activity of nanocapsules loaded with a doxorubicin (DOX) free base dissolved in a core of castor oil shelled by poly(methyl vinyl ether-co-maleic anhydride) conjugated to n-octadecylamine residues.

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20

Chien, Y. Y., Eli M. Pearce, and T. K. Kwei. "Miscibility of poly(vinyl methyl ether) with styrene-methyl methacrylate copolymers." Macromolecules 21, no. 6 (1988): 1616–19. http://dx.doi.org/10.1021/ma00184a015.

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21

Cimmino, Sossio, Emilia Di Pace, Ezio Martuscelli, Clara Silvestre, David M. Rice, and Frank E. Karasz. "Miscibility of syndiotactic polystyrene/poly(vinyl methyl ether) blends." Polymer 34, no. 1 (1993): 214–17. http://dx.doi.org/10.1016/0032-3861(93)90309-x.

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22

Zharov, A. A., O. K. Nikolaeva, and D. I. Moskvin. "Synthesis of perfluoro(methyl vinyl ether) polymer at high pressures." Russian Chemical Bulletin 58, no. 2 (2009): 473–75. http://dx.doi.org/10.1007/s11172-010-0035-1.

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23

Sasaki, Kaito, Masanobu Takatsuka, Rio Kita, Naoki Shinyashiki, and Shin Yagihara. "Enthalpy and Dielectric Relaxation of Poly(vinyl methyl ether)." Macromolecules 51, no. 15 (2018): 5806–11. http://dx.doi.org/10.1021/acs.macromol.8b00780.

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24

Banerjee, Pallab, Mohan L. Digar, Sailendra N. Bhattacharyya, and Broja M. Mandal. "Novel polyaniline dispersions using poly(vinyl methyl ether) stabilizer." European Polymer Journal 30, no. 4 (1994): 499–501. http://dx.doi.org/10.1016/0014-3057(94)90051-5.

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25

Rosiak, Janusz M. "Nano- and Microgels of Poly(Vinyl Methyl Ether) Obtained by Radiation Techniques." Eurasian Chemico-Technological Journal 9, no. 3 (2007): 165–76. https://doi.org/10.18321/ectj289.

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Hydroxyl radicals were generated radiolytically in N2O-saturated aqueous solutions in the presence of poly(vinyl methyl ether) (PVME, 6×104 Da, 10-3-10-2 mol⋅dm-3 in monomer units). As measured by pulse radiolysis, they react (k = 2.2×108 dm3⋅mol-1⋅s-1) with PVME by giving mainly rise to α-alkoxyalkyl radicals (~72%) that reduce (k ≈ 2×109 dm3⋅mol-1⋅s-1) Fe(CN)6 3-, IrCl6 2- or tetranitromethane. Based on the formaldehyde yield in the presence of the latter two oxidants (∼40% of •OH), it is concluded that OH radicals undergo H-abstraction at ROCH2–H, R3C–H and R2HC–H with probabilities of ∼40%

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26

Min, K. E., and D. R. Paul. "Blends of poly(vinyl methyl ether) with styrenic copolymers." Journal of Polymer Science Part B: Polymer Physics 26, no. 11 (1988): 2257–66. http://dx.doi.org/10.1002/polb.1988.090261106.

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27

Patrickios, Costas S., Clive Forder, Steven P. Armes, and Norman C. Billingham. "Synthesis and characterization of amphiphilic diblock copolymers of methyl tri(ethylene glycol) vinyl ether and isobutyl vinyl ether." Journal of Polymer Science Part A: Polymer Chemistry 34, no. 8 (1996): 1529–41. http://dx.doi.org/10.1002/(sici)1099-0518(199606)34:8<1529::aid-pola17>3.0.co;2-a.

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28

Kashparova, Vera P., Victor A. Klushin, Veronika E. Andreeva, Nina V. Smirnova, Irina Yu Zhukova, and Ivan I. Kashparov. "2,5–FURANDICARBOXYLIC ACID DICINAMIL ETHER AND NEW COPOLYMERS ON ITS BASIS." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 63, no. 9 (2020): 4–11. http://dx.doi.org/10.6060/ivkkt.20206309.6246.

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A method for the synthesis of dicinamyl ester of 2,5-furandicarboxylic acid (DCF) a new unsaturated compound of the furan series and potential monomer for producing copolymers with various vinyl compounds and based on them a new generation of construction and ion-exchange materials has been developed. DCF does not form homopolymers as in bulk as in solution (toluene solvent). However, DCF is actively copolymerized with styrene, methyl methacrylate, methacrylic and acrylic acids to form cross-linked polymers with varying degrees of crosslinking. The copolymerization constants of DCF with all in

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29

Gardner, Casandra M., Nicholas A. D. Burke, Terry Chu, Feng Shen, Murray A. Potter, and Harald D. H. Stöver. "Poly(methyl vinyl ether-alt-maleic acid) Polymers for Cell Encapsulation." Journal of Biomaterials Science, Polymer Edition 22, no. 16 (2011): 2127–45. http://dx.doi.org/10.1163/092050610x535149.

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30

Kitade, Shinichi, Kenji Ochiai, Megumi Ida, Yoshiaki Takahashi, and Ichiro Noda. "Plateau Modulus of Homogeneous Polystyrene/Poly(vinyl methyl ether) Blends." Polymer Journal 29, no. 12 (1997): 1034–36. http://dx.doi.org/10.1295/polymj.29.1034.

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31

Yin, Huajie, and Andreas Schönhals. "Calorimetric glass transition of ultrathin poly(vinyl methyl ether) films." Polymer 54, no. 8 (2013): 2067–70. http://dx.doi.org/10.1016/j.polymer.2013.02.025.

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32

McHerron, Dale C., and Garth L. Wilkes. "Electron beam irradiation of polystyrene-poly(vinyl methyl ether) blends." Polymer 34, no. 19 (1993): 3976–85. http://dx.doi.org/10.1016/0032-3861(93)90657-v.

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33

Shiomi, Tomoo, Fumiyuki Hamada, Tadao Nasako, Kohji Yoneda, Kiyokazu Imai, and Akio Nakajima. "Thermodynamics of polymer blends of poly(vinyl methyl ether) and polystyrene." Macromolecules 23, no. 1 (1990): 229–33. http://dx.doi.org/10.1021/ma00203a039.

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34

Chien, Y. Y., Eli M. Pearce, and T. K. Kwei. "Photooxidation of blends of polystyrene and poly (vinyl methyl ether)." Journal of Polymer Science Part A: Polymer Chemistry 29, no. 6 (1991): 849–56. http://dx.doi.org/10.1002/pola.1991.080290609.

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35

Chahid, A., A. Alegria, and J. Colmenero. "Methyl Group Dynamics in Poly(vinyl methyl ether). A Rotation Rate Distribution Model." Macromolecules 27, no. 12 (1994): 3282–88. http://dx.doi.org/10.1021/ma00090a022.

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36

Shiomi, Tomoo, Katsumi Kohno, Kohji Yoneda, Tetsuo Tomita, Masamitsu Miya, and Kiyokazu Imai. "Thermodynamic interactions in the poly(vinyl methyl ether)-polystyrene system." Macromolecules 18, no. 3 (1985): 414–19. http://dx.doi.org/10.1021/ma00145a020.

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37

Pernecker, Tibor, Joseph P. Kennedy, and Bela Ivan. "Living carbocationic polymerization. 48. Poly(isobutylene-b-methyl vinyl ether)." Macromolecules 25, no. 6 (1992): 1642–47. http://dx.doi.org/10.1021/ma00032a004.

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38

Van Durme, Kurt, Els Loozen, Erik Nies, and Bruno Van Mele. "Phase Behavior of Poly(vinyl methyl ether) in Deuterium Oxide." Macromolecules 38, no. 24 (2005): 10234–43. http://dx.doi.org/10.1021/ma051745y.

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39

Arndt, Karl-Fr, Thomas Schmidt, and Heike Menge. "Poly(vinyl methyl ether) hydrogel formed by high energy irradiation." Macromolecular Symposia 164, no. 1 (2001): 313–22. http://dx.doi.org/10.1002/1521-3900(200102)164:1<313::aid-masy313>3.0.co;2-d.

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40

Markova, Dilyana, Darinka Christova, and Rumiana Velichkova. "Synthesis of novel poly(vinyl methyl ether) copolymers by alkylation of poly(vinyl acetate) and poly(vinyl alcohol)." Polymer International 52, no. 10 (2003): 1600–1604. http://dx.doi.org/10.1002/pi.1346.

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41

Saidi, Abdullah Khamis Ali Al, Adibehalsadat Ghazanfari, Shuwen Liu, et al. "Facile Synthesis and X-ray Attenuation Properties of Ultrasmall Platinum Nanoparticles Grafted with Three Types of Hydrophilic Polymers." Nanomaterials 13, no. 5 (2023): 806. http://dx.doi.org/10.3390/nano13050806.

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Ultrasmall platinum nanoparticles (Pt-NPs) grafted with three types of hydrophilic and biocompatible polymers, i.e., poly(acrylic acid), poly(acrylic acid-co-maleic acid), and poly(methyl vinyl ether-alt-maleic acid) were synthesized using a one-pot polyol method. Their physicochemical and X-ray attenuation properties were characterized. All polymer-coated Pt-NPs had an average particle diameter (davg) of 2.0 nm. Polymers grafted onto Pt-NP surfaces exhibited excellent colloidal stability (i.e., no precipitation after synthesis for >1.5 years) and low cellular toxicity. The X-ray attenuatio

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42

Tran-Cong, Q., H. Nakano, J. Okinaka, and R. Kawakubo. "Miscibility of poly(2-chlorostyrene) and poly(vinyl methyl ether) blends." Polymer 35, no. 6 (1994): 1242–47. http://dx.doi.org/10.1016/0032-3861(94)90018-3.

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43

Digar, M. L., S. N. Bhattacharyya, and B. M. Mandal. "Dispersion polymerization of pyrrole using poly(vinyl methyl ether) as stabilizer." Polymer 35, no. 2 (1994): 377–82. http://dx.doi.org/10.1016/0032-3861(94)90707-2.

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44

Kabra, B. G., M. K. Akhtar, and S. H. Gehrke. "Volume change kinetics of temperature-sensitive poly(vinyl methyl ether) gel." Polymer 33, no. 5 (1992): 990–95. http://dx.doi.org/10.1016/0032-3861(92)90014-n.

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45

Uriarte, C., J. I. Eguiazabal, M. Llanos, J. I. Iribarren, and J. J. Iruin. "Miscibility and phase separation in poly(vinyl methyl ether)/poly(bisphenol A hydroxy ether) blends." Macromolecules 20, no. 12 (1987): 3038–42. http://dx.doi.org/10.1021/ma00178a016.

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46

Seetapan, Kriengkrai, and Taeng On Prommi. "Microplastics in commercial fish digestive tracts from freshwater habitats in Northern Thailand." Ecologica Montenegrina 68 (November 3, 2023): 48–65. http://dx.doi.org/10.37828/em.2023.68.6.

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Microplastics (MPs) contamination in fish species was one of the emerging environmental issues as a result of the widespread presence of plastic pollution in the environment. The presence of MPs in Thailand's freshwater was scant, and in contrast to other countries, little was known about the presence of this contaminant in freshwater fish. Hence, the purpose of this study was to examine the abundance, characteristics, and variation of MPs in various Thai commercial freshwater fish species. In order to compare the differences in MP ingestion rates across different feeding zones, 166 fish repre

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47

Park, Hyunkil, Eli M. Pearce, and T. K. Kwei. "Thermal oxidation of blends of polystyrene and poly(vinyl methyl ether)." Macromolecules 23, no. 2 (1990): 434–41. http://dx.doi.org/10.1021/ma00204a015.

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48

Rotstein, N. A., and T. P. Lodge. "Tracer diffusion of linear polystyrenes in poly(vinyl methyl ether) gels." Macromolecules 25, no. 4 (1992): 1316–25. http://dx.doi.org/10.1021/ma00030a018.

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49

Butler, George B., Choon H. Do, and Michael C. Zerner. "Localized bond (PVCILO) calculations on the cyanoethylenes-methyl vinyl ether complexes." Macromolecules 25, no. 7 (1992): 1858–63. http://dx.doi.org/10.1021/ma00033a003.

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50

Etxeberria, A., J. J. Iruin, A. Unanue, P. J. Iriondo, M. J. Fernandez-Berridi, and A. Martinez de Ilarduya. "Miscibility windows of poly(vinyl methyl ether) with modified phenoxy resin." European Polymer Journal 37, no. 10 (2001): 1943–50. http://dx.doi.org/10.1016/s0014-3057(01)00092-1.

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