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Journal articles on the topic 'Butyl methacrylate'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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1

Fukumoto, Aoi, Miharu Arimoto, Shin-ichi Matsuoka, and Masato Suzuki. "Polycondensation of methacrylates: auto-tandem organocatalysis using N-heterocyclic carbenes." Polymer Chemistry 9, no. 43 (2018): 5295–302. http://dx.doi.org/10.1039/c8py01027g.

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N-Heterocyclic carbenes catalyzed the self-polycondensation of hydroxy-functionalized methacrylates and the direct polycondensation of n-butyl methacrylate with diols to produce new unsaturated polyesters.

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2

Novakovic, Katarina, Lynne Katsikas, and Ivanka Popovic. "The thermal degradation of poly(iso-butyl methacrylate) and poly(sec-butyl methacrylate)." Journal of the Serbian Chemical Society 65, no. 12 (2000): 867–75. http://dx.doi.org/10.2298/jsc0012867n.

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The non-oxidative thermal degradation of poly(iso-butyl methacrylate) and poly(sec-butyl methacrylate) was investigated by studying changes in the polymer residue. Due to the different number of ?-hydrogens in their ester substituents, these two polymeric isomers behave differently when subjected to elevated temperatures. Poly(iso-butyl methacrylate) degrades quantitatively by depolymerisation with zip lengths of the same order of magnitude as those of poly(methyl methacrylate). Poly(sec-butyl methacrylate) degrades by a combined degradation mechanism of depolymerisation and de-esterification.

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3

Serheyev, Valentyn, and Tran Van Thanh. "Thermodynamic Properties of Butyl Methacrylate Solutions in Organic Solvents." Chemistry & Chemical Technology 12, no. 1 (2018): 7–12. http://dx.doi.org/10.23939/chcht12.01.007.

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4

Buback, Michael, and Thomas Junkers. "Termination Kinetics oftert-Butyl Methacrylate and ofn-Butyl Methacrylate Free-Radical Bulk Homopolymerizations." Macromolecular Chemistry and Physics 207, no. 18 (2006): 1640–50. http://dx.doi.org/10.1002/macp.200600254.

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5

Shushunova, N. Yu, M. V. Arsenyev, T. A. Glukhova, S. D. Zaitsev, and S. A. Chesnokov. "Polymerization of butyl acrylate and butyl methacrylate in the presence of o-quinone methacrylate." Polymer Science Series B 57, no. 3 (2015): 207–16. http://dx.doi.org/10.1134/s1560090415030070.

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6

Yu, Li, Yong Kui Huang, Guo Bin Duan, and Shui Jin Yang. "Catalytic Synthesis of N-Butyl Methacrylate with H₄SiW₆Mo₆O₄₀/SiO₂." Advanced Materials Research 631-632 (January 2013): 135–39. http://dx.doi.org/10.4028/www.scientific.net/amr.631-632.135.

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A novel environmental friendly catalyst, H4SiW6Mo6O40/SiO2was synthesized by a sol-gel technique, and characterized by FT-IR and XRD. Catalytic application of the catalyst for synthesis of n-butyl methacrylate was investigated. The variation of different reaction parameters were studied by orthogonal design. Under optimized conditions, that is, molar ratio of methacrylic acid to n-butanol is 1:1.7, catalyst dosage is 0.75 %, volume of cyclohexane is 12 mL and the reaction time is 2.5 h, the yield of n-butyl methacrylate reaches 85.3%. The results reveal that the H4SiW6Mo6O40/SiO2O2 catalysis i

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7

Mirau, Peter A., and Mohan Srentvasarao. "NMR Characterization of Liquid Crystal—Polymer Interactions in Polymer-Dispersed Liquid Crystals." Applied Spectroscopy 51, no. 11 (1997): 1639–43. http://dx.doi.org/10.1366/0003702971939299.

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Solid-state nuclear magnetic resonance (NMR) and optical microscopy have been used to study liquid crystal–polymer interactions in polymer-dispersed liquid crystals (PDLCs) composed of the E7 liquid crystal mixture and poly( n-butyl methacrylate) or poly(isobutyl methacrylate). As previously reported, the droplets adopt a bipolar configuration in the PDLCs using poly( n-butyl methacrylate) as the matrix material and a radial configuration in those using poly(isobutyl methacrylate). The NMR signals from the E7 cannot be detected in the bulk state by using magic angle spinning and cross-polariza

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8

Negim, E. S. M., A. Nurlybayeva, G. S. Irmukhametova, et al. "Effect of methyl methacrylate and butyl methacrylate copolymer on the physico-mechanical properties of acryl syrup for paints." International Journal of Biology and Chemistry 8, no. 2 (2015): 60–65. http://dx.doi.org/10.26577/2218-7979-2015-8-2-60-65.

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9

Ha, Dong-Myeong. "Measurement and Prediction of the Combustible Properties of n-Butyl methacrylate(n-BMA)." Journal of the Korean Society of Safety 31, no. 4 (2016): 42–47. http://dx.doi.org/10.14346/jkosos.2016.31.4.42.

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10

Guo, Tian-Ying, Donglin Tang, Moudao Song, and Banghua Zhang. "Copolymerizations of butyl methacrylate and fluorinated methacrylates via RAFT miniemulsion polymerization." Journal of Polymer Science Part A: Polymer Chemistry 45, no. 22 (2007): 5067–75. http://dx.doi.org/10.1002/pola.22249.

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11

Bradley, Melanie, Brian Vincent, and Gary Burnett. "Biocompatible, Polyampholyte Microgel Particles." Australian Journal of Chemistry 60, no. 9 (2007): 646. http://dx.doi.org/10.1071/ch07098.

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Biocompatible, polyampholyte microgel particles have been prepared by the acid hydrolysis of t-butyl groups within (2-diethylamino)ethyl methacrylate-co-t-butyl methacrylate microgel particles to give (2-diethylamino)ethyl methacrylate-co-methacrylic acid microgel particles. The hydrodynamic diameter and electrophoretic mobility of both the pre-hydrolyzed and post-hydrolyzed microgel particles have been investigated as a function of pH for three microgel dispersions differing in their monomer compositions. The swelling properties and isoelectric point pH are shown to depend on the monomer comp

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12

Choi, Weon-Jung, Yang-Bae Kim, Soon-Ki Kwon, Kwon-Taek Lim, and Sam-Kwon Choi. "Synthesis, characterization, and modification of poly(tert-butyl methacrylate-b-alkyl methacrylate-b-tert-butyl methacrylate) by group transfer polymerization." Journal of Polymer Science Part A: Polymer Chemistry 30, no. 10 (1992): 2143–48. http://dx.doi.org/10.1002/pola.1992.080301007.

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13

Soriano-Corral, F., L. F. Ramos-de Valle, F. J. Enríquez-Medrano, P. A. De León-Martínez, M. L. López-Quintanilla, and E. N. Cabrera-Álvarez. "Cast Nanostructured Films of Poly(methyl methacrylate-b-butyl acrylate)/Carbon Nanotubes: Influence of Poly(butyl acrylate) Content on Film Evaporation Rate, Morphology, and Electrical Resistance." Journal of Nanomaterials 2012 (2012): 1–8. http://dx.doi.org/10.1155/2012/352937.

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Nanocomposites of poly(methyl methacrylate-b-butyl acrylate)/multiwalled carbon nanotubes were prepared from different copolymers synthesized by RITP technique using iodine functionalized poly(methyl methacrylate) as macrochain transfer agent to obtain block copolymers with butyl acrylate as comonomer in a sequential copolymerization. Poly(butyl acrylate) contents of 7, 20, and 30 wt% were attained in each copolymer. These copolymers were used to prepare nanostructured films by casting process, using chloroform as solvent, and carboxyl functionalized MWCNT at 0.4, 0.6, 0.8, 1.0, and 1.2 wt%. D

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14

SHOJI, Kikuo, Yukio NAKAJIMA, Eiichi UEDA, and Masatami TAKEDA. "Liquid crystalline properties of cholesteryl methacrylate and butyl methacrylate copolymers." KOBUNSHI RONBUNSHU 42, no. 8 (1985): 489–94. http://dx.doi.org/10.1295/koron.42.489.

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15

Erhardt, Peter F., James M. O'Reilly, W. Conrad Richards, and Meurig W. Williams. "Viscoelastic behavior of styrene/n-butyl-methacrylate/potassium methacrylate polymers." Journal of Polymer Science: Polymer Symposia 45, no. 1 (2007): 139–51. http://dx.doi.org/10.1002/polc.5070450112.

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16

Shoji, Kikuo, Yukio Nakajima, Eiichi Ueda, and Masatami Takeda. "Thermal Optical Analysis of Cholesteryl Methacrylate and Butyl Methacrylate Copolymers." Polymer Journal 17, no. 9 (1985): 1029–36. http://dx.doi.org/10.1295/polymj.17.1029.

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17

Sixou, B., and C. Menissez. "Molecular Mobility in Poly(butyl methacrylate) and Poly(methyl methacrylate)." Molecular Simulation 30, no. 8 (2004): 521–28. http://dx.doi.org/10.1080/0892702042000207764.

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18

Zhang, Yujie, and Marc Arnold Dubé. "Copolymerization ofn-Butyl Methacrylate andD-Limonene." Macromolecular Reaction Engineering 8, no. 12 (2014): 805–12. http://dx.doi.org/10.1002/mren.201400023.

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19

Moulder, J. F., W. F. Stickle, and P. E. Sobol. "Poly (iso‐butyl methacrylate) by XPS." Surface Science Spectra 1, no. 4 (1992): 356–60. http://dx.doi.org/10.1116/1.1247632.

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20

Moulder, J. F., W. F. Stickle, and P. E. Sobol. "Poly (n‐butyl methacrylate) by XPS." Surface Science Spectra 1, no. 4 (1992): 351–55. http://dx.doi.org/10.1116/1.1247666.

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21

Baruah, S. D., and B. Subrahmanyam. "Charge-transfer polymerization of butyl methacrylate." Colloid & Polymer Science 269, no. 6 (1991): 543–46. http://dx.doi.org/10.1007/bf00659906.

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22

Ren, Shanshan, Lisha Zhang, and Marc A. Dubé. "Free-radical terpolymerization ofn-butyl acrylate/butyl methacrylate/d-limonene." Journal of Applied Polymer Science 132, no. 47 (2015): n/a. http://dx.doi.org/10.1002/app.42821.

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23

Li, Jieming, and Mario Gauthier. "Synthesis of ?- and ?,?-sulfonatotelechelics based on homopolymers and block copolymers ofn-butyl methacrylate andt-butyl methacrylate." Journal of Polymer Science Part A: Polymer Chemistry 38, no. 20 (2000): 3711–21. http://dx.doi.org/10.1002/1099-0518(20001015)38:20<3711::aid-pola10>3.0.co;2-h.

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24

Katime, Issa, and Ana Cadenato. "Compatibility of peo/poly(iso-butyl methacrylate) and peo/poly(tert-butyl methacrylate) blends by DTA." Materials Letters 22, no. 5-6 (1995): 303–8. http://dx.doi.org/10.1016/0167-577x(94)00264-9.

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25

Zhang, Guoqing, Changwei Cai, Yilai Wang, et al. "Preparation and evaluation of thermo-regulating bamboo fabric treated by microencapsulated phase change materials." Textile Research Journal 89, no. 16 (2018): 3387–93. http://dx.doi.org/10.1177/0040517518813681.

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Two types of microencapsulated phase change materials (ENPCMs) were synthesized by polymerization. The core material of ENPCM was n-octadecane and the shell materials were polymethyl methacrylate-butyl acrylate and polymethyl methacrylate-butyl acrylate-hydroxyethyl methacrylate. Subsequently, the synthesized ENPCMs were applied onto bamboo fabric by the dip and dry method. The properties of ENPCMs were analyzed in terms of surface morphology, size distribution and latent heat; the treated bamboo fabrics were evaluated in terms of surface morphology, hydrophilicity, washing fastness and heat s

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26

Linh, Nguyen-Vu Viet, Nguyen Trung Duc, and Huynh Dai Phu. "Copolymerization of n-butyl acrylate/methyl methacrylate in xylene solvent." Science and Technology Development Journal 22, no. 1 (2019): 120–27. http://dx.doi.org/10.32508/stdj.v22i1.1020.

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Introduction: Copolymers are being used in a variety of fields because of their diversity and since any change could result in significant modifications. The butyl acrylate/methyl methacrylate copolymer is an extensively used polymer system with many advantages. This study aims to analyze some changes in copolymerization, from using different time or temperature of synthesis, in order to find an optimal process that can be applied in Vietnam. Methods: Copolymerization of butyl acrylate/methyl methacrylate copolymer with different butyl acrylate/methyl methacrylate monomer ratios was done

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27

Tao, Lei, Zeyu Sun, Wei Min, Hanwen Ou, Liangliang Qi, and Muhuo Yu. "Improving the toughness of thermosetting epoxy resins via blending triblock copolymers." RSC Advances 10, no. 3 (2020): 1603–12. http://dx.doi.org/10.1039/c9ra09183a.

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28

Deporter, Craig D., Timothy E. Long, and James E. McGrath. "Methacrylate-based block ionomers I: Synthesis of block ionomers derived from t-butyl methacrylate and alkyl methacrylates." Polymer International 33, no. 2 (1994): 205–16. http://dx.doi.org/10.1002/pi.1994.210330212.

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29

Belaidi, O., T. Bouchaour, and U. Maschke. "Accuracy and Applicability of the New Exchange Correlation Functionals for Reproduction of the Infrared Spectra of Butyl Acrylate and Butyl Methacrylate Molecules." Organic Chemistry International 2013 (October 9, 2013): 1–12. http://dx.doi.org/10.1155/2013/834520.

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The butyl acrylate and butyl methacrylate were optimized by seven functionals. All the structures found are local minima and belong to the Cs symmetry. The calculated frequencies are scaled and ranked according to their square errors. The scaling factors of the B972 and B98 functionals fail to reproduce the infrared spectra. The calculated and scaled frequencies with G96LYP, OLYP, and HCTH functionals give acceptable correlations with the experimental spectra. The scaling factors for O3LYP/6-31G(f,p) and O3LYP/6-311+G(df,p) levels of theory reproduce very well the infrared spectrum of butyl ac

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30

Dorsman, Isabella R., Matthew J. Derry, Victoria J. Cunningham, Steven L. Brown, Clive N. Williams, and Steven P. Armes. "Tuning the vesicle-to-worm transition for thermoresponsive block copolymer vesicles prepared via polymerisation-induced self-assembly." Polymer Chemistry 12, no. 9 (2021): 1224–35. http://dx.doi.org/10.1039/d0py01713b.

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Does statistical copolymerization of n-butyl methacrylate with benzyl methacrylate lower the critical temperature required for vesicle-to-worm and worm-to-sphere transitions for diblock copolymer nano-objects in mineral oil?

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31

Mori, Sadao. "Liquid adsorption chromatography of styrene-alkyl methacrylate copolymers and ethyl methacrylate-butyl methacrylate copolymers." Polymer 32, no. 12 (1991): 2230–33. http://dx.doi.org/10.1016/0032-3861(91)90051-j.

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32

Barth, Johannes, Michael Buback, Pascal Hesse, and Tatiana Sergeeva. "Chain-Length-Dependent Termination inn-Butyl Methacrylate andtert-Butyl Methacrylate Bulk Homopolymerizations Studied via SP-PLP-ESR." Macromolecules 42, no. 2 (2009): 481–88. http://dx.doi.org/10.1021/ma802078g.

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33

Loveday, Don, Garth L. Wilkes, Craig D. Deporter, and James E. McGrath. "Structure and Properties of Butadiene-tert-Butyl Methacrylate and Butadiene/Styrene-tert-Butyl Methacrylate Triblock Copolymer Ionomers." Macromolecules 28, no. 23 (1995): 7822–30. http://dx.doi.org/10.1021/ma00127a032.

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34

Lim, Byung-Yun, and Sung-Chul Kim. "Morphology of crosslinked poly(butyl methacrylate-co-methyl methacrylate) porous membranes." Journal of Membrane Science 209, no. 1 (2002): 293–307. http://dx.doi.org/10.1016/s0376-7388(02)00357-5.

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35

Mishra, Sujata, Jagbir Singh, and Veena Choudhary. "Synthesis and characterization of butyl acrylate/methyl methacrylate/glycidyl methacrylate latexes." Journal of Applied Polymer Science 115, no. 1 (2010): 549–57. http://dx.doi.org/10.1002/app.30963.

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36

Feng, Y., and C. F. Xiao. "Research on butyl methacrylate–lauryl methacrylate copolymeric fibers for oil absorbency." Journal of Applied Polymer Science 101, no. 3 (2006): 1248–51. http://dx.doi.org/10.1002/app.22798.

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37

Kapur, G. S., and A. S. Brar. "Methyl methacrylate-n-butyl methacrylate copolymer containing ferric chloride: Mössbauer study." Journal of Radioanalytical and Nuclear Chemistry Letters 136, no. 3 (1989): 169–75. http://dx.doi.org/10.1007/bf02164115.

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38

Buback, Michael, and Christopher Kowollik. "Termination kinetics in free-radical bulk terpolymerization — the systems methyl acrylate - butyl acrylate - dodecyl acrylate and methyl methacrylate - butyl methacrylate - dodecyl methacrylate." Macromolecular Chemistry and Physics 200, no. 7 (1999): 1764–70. http://dx.doi.org/10.1002/(sici)1521-3935(19990701)200:7<1764::aid-macp1764>3.0.co;2-f.

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39

Wisniak, Jaime, Gladis Cortez, René D. Peralta, et al. "Volumetric Properties of the Ternary System Dimethyl Carbonate + Butyl Methacrylate + Allyl Methacrylate and Its Binary Butyl Methacrylate + Allyl Methacrylate at 293.15 K and p=101.325 kPa." Journal of Solution Chemistry 41, no. 9 (2012): 1631–48. http://dx.doi.org/10.1007/s10953-012-9892-6.

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40

Grady, Michael C., William J. Simonsick, and Robin A. Hutchinson. "Studies of higher temperature polymerization ofn-butyl methacrylate andn-butyl acrylate." Macromolecular Symposia 182, no. 1 (2002): 149–68. http://dx.doi.org/10.1002/1521-3900(200206)182:1<149::aid-masy149>3.0.co;2-d.

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41

Li, Deheng, and Robin A. Hutchinson. "Penultimate Propagation Kinetics of Butyl Methacrylate, Butyl Acrylate, and Styrene Terpolymerization." Macromolecular Rapid Communications 28, no. 11 (2007): 1213–18. http://dx.doi.org/10.1002/marc.200700149.

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42

Rosselle, Léa, Anna Rita Cantelmo, Alexandre Barras, et al. "An ‘on-demand’ photothermal antibiotic release cryogel patch: evaluation of efficacy on an ex vivo model for skin wound infection." Biomaterials Science 8, no. 21 (2020): 5911–19. http://dx.doi.org/10.1039/d0bm01535k.

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NIR-light activable cryogels based on butyl methacrylate and poly(ethylene glycol) methyl ether methacrylate modified with reduced graphene oxide and loaded with cefepime was tested on an infected ex vivo skin model as skin regeneration scaffold.

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43

Ishizu, Koji, Kenji Mitsutani, and Takashi Fukutomi. "Synthesis of poly(t-butyl methacrylate) macromonomer." Journal of Polymer Science Part C: Polymer Letters 25, no. 7 (1987): 287–91. http://dx.doi.org/10.1002/pol.1987.140250703.

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44

KATAKURA, Naoyuki, Makoto HOSOTANI, Kazunori IIJIMA, Hisao HONMA, and Midori SAKAGUCHI. "Tissue Conditioners Containing Poly (butyl methacrylate) Powder." Dental Materials Journal 8, no. 1 (1989): 35–39. http://dx.doi.org/10.4012/dmj.8.35.

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45

Bataille, Pierre, Marjan Almassi, and Mitsuo Inoue. "Emulsifier-free emulsion polymerization ofN-butyl methacrylate." Journal of Applied Polymer Science 67, no. 10 (1998): 1711–19. http://dx.doi.org/10.1002/(sici)1097-4628(19980307)67:10<1711::aid-app4>3.0.co;2-m.

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46

Jovanović, Renata, Keltoum Ouzineb, Timothy F. McKenna, and Marc A. Dubé. "Butyl acrylate/methyl methacrylate latexes: adhesive properties." Macromolecular Symposia 206, no. 1 (2004): 43–56. http://dx.doi.org/10.1002/masy.200450204.

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47

Liu, Yuanqin, Walter Schroeder, Mohsen Soleimani, Willie Lau, and Mitchell A. Winnik. "Effect of Hyperbranched Poly(butyl methacrylate) on Polymer Diffusion in Poly(butyl acrylate-co-methyl methacrylate) Latex Films." Macromolecules 43, no. 15 (2010): 6438–49. http://dx.doi.org/10.1021/ma100483e.

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48

Yao, Xue Rong, Fang Chen, Zhao Xia Guo, and Jian Yu. "Polypropylene/poly(butyl methacrylate) blends prepared by diffusion and subsequent polymerization of butyl methacrylate in isotactic polypropylene pellets." Chinese Chemical Letters 23, no. 6 (2012): 753–56. http://dx.doi.org/10.1016/j.cclet.2012.03.031.

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49

Miranda, Larissa N., and Warren T. Ford. "Binary copolymer reactivity oftert-butyl methacrylate, 2-(N,N-dimethylamino)ethyl methacrylate, solketal methacrylate, and 2-bromoethyl methacrylate." Journal of Polymer Science Part A: Polymer Chemistry 43, no. 19 (2005): 4666–69. http://dx.doi.org/10.1002/pola.20939.

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50

Fang, Zhou, and Qing Zhi Dong. "Preparation, Damping and Thermal Properties of Castor Oil-Based Polyurethane/Poly(Methyl Methacrylate-Butyl Methacrylate-Styrene) Grafted Interpenetrating Polymer Networks." Advanced Materials Research 1096 (April 2015): 455–64. http://dx.doi.org/10.4028/www.scientific.net/amr.1096.455.

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A series of castor oil-based polyurethane (PU)/poly (methyl methacrylate-butyl methacrylate-styrene) (PA) grafted interpenetrating polymer networks (IPNs) were prepared. The effect of composition of the IPNs on the damping, thermal and mechanical properties were studied systematically. PU/PA (60:40, weight ratio) IPNs with methyl methacrylate/butyl methacrylate/styrene (MMA/BMA/St = 80/10/10, weight ratio). In the paper castor oil (CO) was used as PU’s branch units, the damping properties affected by the branch units ratio (ρ) were studied. Mechanical tests showed the tensile strength of the I

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