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Journal articles on the topic 'Trimethylolpropane trimethacrylate'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 February 2022

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1

Schmid, Andrea, Maria Walenius, and Per Flodin. "Mechanical stability of trimethylolpropane trimethacrylate-based polymers." Journal of Applied Polymer Science 45, no. 11 (1992): 1995–2004. http://dx.doi.org/10.1002/app.1992.070451114.

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2

Craciun, Gabriela, Elena Manaila, and Maria Daniela Stelescu. "Electron Beam Synthesis and Characterization of Acrylamide/Acrylic Acid Hydrogels Using Trimethylolpropane Trimethacrylate as Cross-Linker." Journal of Chemistry 2016 (2016): 1–14. http://dx.doi.org/10.1155/2016/1470965.

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The purpose of the paper is to present the synthesis and characterization of hydrogels prepared by free-radical copolymerization of acrylamide and acrylic acid in aqueous solutions using potassium persulfate as initiator and trimethylolpropane trimethacrylate as cross-linker, via the radiation technique. The samples were subjected to electron beam treatment in the dose range of 2 to 4 kGy and the influence of the absorbed dose and amount of cross-linker on the swelling properties, diffusion coefficient, and network parameters of hydrogels was investigated. A possible reaction mechanism for acr

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3

Zeng, Shaomei, Yongxin She, Bining Jiao, et al. "Molecularly imprinted polymer for selective extraction and simultaneous determination of four tropane alkaloids from Przewalskia tangutica Maxim. fruit extracts using LC-MS/MS." RSC Advances 5, no. 115 (2015): 94997–5006. http://dx.doi.org/10.1039/c5ra18608k.

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A class-specific molecularly imprinted polymer (MIP) for selectively extracting four tropane alkaloids has been prepared using anisodine, methacrylic, and trimethylolpropane trimethacrylate as template, functional monomer and crosslinker, respectively.

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4

Chen, Jianfu, Weiying Zhang, and Xiao Li. "Preparation and characterization of a novel superabsorbent of konjac glucomannan-poly(acrylic acid) with trimethylolpropane trimethacrylate cross-linker." RSC Advances 5, no. 48 (2015): 38417–23. http://dx.doi.org/10.1039/c5ra04522c.

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A novel superabsorbent was prepared by the solution polymerization of partially neutralized acrylic acid onto konjac glucomannan using potassium persulfate as a free radical initiator and trimethylolpropane trimethacrylate as a crosslinking agent.

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5

Teixeira Tarley, César Ricardo, Mariana Gava Segatelli, Juliana Casarin, and Raquel Justo da Fonseca. "New sorbents based on poly(methacrylic acid-TRIM) and poly(vinylimidazole-TRIM) for simultaneous preconcentration of herbicides in water samples with posterior determination by HPLC-DAD." RSC Advances 7, no. 60 (2017): 37959–66. http://dx.doi.org/10.1039/c7ra04124a.

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In the present study, poly(methacrylic acid-trimethylolpropane trimethacrylate) (PMA-TRIM) and poly(vinylimidazole-TRIM) (PV-TRIM) have been used for simultaneous extraction of tebuthiuron, hexazinone, diuron, and ametryn with posterior determination by HPLC-DAD.

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6

Schmid, A. B., and P. Flodin. "Hydrophilic gels of poly(trimethylolpropane trimethacrylate-co-acrylamide)." Reactive Polymers 15 (November 1991): 49–54. http://dx.doi.org/10.1016/0923-1137(91)90146-f.

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7

Harrell, J. W., and S. J. Ahuja. "A relaxation time study of molecular motion in trimethylolpropane triacrylate and trimethylolpropane trimethacrylate." Chemical Physics 138, no. 2-3 (1989): 383–90. http://dx.doi.org/10.1016/0301-0104(89)87144-7.

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8

Rosenberg, J. E., and P. Flodin. "Macroporous gels. 1. Polymerization of trimethylolpropane trimethacrylate in toluene." Macromolecules 19, no. 6 (1986): 1543–46. http://dx.doi.org/10.1021/ma00160a011.

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9

Harrell, J. W., Mubinur Choudhury, Sanjay Ahuja, and William Walker. "An NMR study of the electron beam-induced polymerization of trimethylolpropane triacrylate and trimethylolpropane trimethacrylate." Journal of Polymer Science Part B: Polymer Physics 29, no. 9 (1991): 1039–46. http://dx.doi.org/10.1002/polb.1991.090290901.

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10

Dhal, Pradeep K., S. Vidyasankar, and Frances H. Arnold. "Surface Grafting of Functional Polymers to Macroporous Poly(trimethylolpropane trimethacrylate)." Chemistry of Materials 7, no. 1 (1995): 154–62. http://dx.doi.org/10.1021/cm00049a024.

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11

Rosenberg, J. E., and P. Flodin. "Macroporous gels. 2. Polymerization of trimethylolpropane trimethacrylate in various solvents." Macromolecules 20, no. 7 (1987): 1518–22. http://dx.doi.org/10.1021/ma00173a013.

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12

Matsumoto, Akira, Hiroyuki Ando, and Masayashi Oiwa. "Gelation in the copolymerization of methyl methacrylate with trimethylolpropane trimethacrylate." European Polymer Journal 25, no. 4 (1989): 385–89. http://dx.doi.org/10.1016/0014-3057(89)90155-9.

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13

Rahman, Nazia, Mubarak A. Khan, Ruhul A. Khan, and Tofail A. Chowdhury. "Modification of Gelatin Films Using Trimethylolpropane Trimethacrylate (TMPTMA) by Photo-Curing." Polymer-Plastics Technology and Engineering 50, no. 4 (2011): 404–11. http://dx.doi.org/10.1080/03602559.2010.543230.

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14

Matsumoto, Akira, Noriyasu Murakami, Hiroyuki Aota, Jun-ichi Ikeda, and Ignac Capek. "Emulsion polymerization of lauryl methacrylate and its copolymerization with trimethylolpropane trimethacrylate." Polymer 40, no. 20 (1999): 5687–90. http://dx.doi.org/10.1016/s0032-3861(98)00789-7.

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15

Tayebi, Seyed Saeid, Yousef Jahani, and Hassan Arabi. "Trimethylolpropane trimethacrylate functionalized polypropylene/polyhexene-1 blend with enhanced melt strength." Polymer-Plastics Technology and Materials 59, no. 5 (2019): 555–71. http://dx.doi.org/10.1080/25740881.2019.1669653.

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16

Schmid, Andrea B., and Per Flodin. "Hydrophilic poly(trimethylolpropane trimethacrylate-CO-N,N′-methylene-bis-acrylamide) gels." European Polymer Journal 29, no. 4 (1993): 469–74. http://dx.doi.org/10.1016/0014-3057(93)90002-w.

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17

Datta, Sujit K., A. K. Bhowmick, T. K. Chaki, A. B. Majali, and R. S. Despande. "Electron beam initiated modification of ethylene vinyl acetate using trimethylolpropane trimethacrylate." Polymer 37, no. 1 (1996): 45–55. http://dx.doi.org/10.1016/0032-3861(96)81598-9.

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18

Tai, Horng-Jer. "Molecular structural evolution in crosslinking low density polyethylene-trimethylolpropane trimethacrylate systems." Polymer Engineering & Science 41, no. 1 (2001): 95–106. http://dx.doi.org/10.1002/pen.10712.

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19

da Fonseca, Raquel Justo, Mariana Gava Segatelli, Keyller Bastos Borges, and César Ricardo Teixeira Tarley. "Synthesis and evaluation of different adsorbents based on poly(methacrylic acid–trimethylolpropane trimethacrylate) and poly(vinylimidazole–trimethylolpropane trimethacrylate) for the adsorption of tebuthiuron from aqueous medium." Reactive and Functional Polymers 93 (August 2015): 1–9. http://dx.doi.org/10.1016/j.reactfunctpolym.2015.05.004.

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20

Grochowicz, Marta, Łukasz Szajnecki, and Barbara Gawdzik. "4-Vinylpyridine–Trimethylolpropane Trimethacrylate Composite Polymer Particles and Their Application as Adsorbents." Adsorption Science & Technology 33, no. 6-8 (2015): 609–16. http://dx.doi.org/10.1260/0263-6174.33.6-8.609.

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21

Grochowicz, Marta. "Investigation of the thermal behavior of 4-vinylpyridine–trimethylolpropane trimethacrylate copolymeric microspheres." Journal of Thermal Analysis and Calorimetry 118, no. 3 (2014): 1603–11. http://dx.doi.org/10.1007/s10973-014-4066-y.

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22

Mousavi-Saghandikolaei, Seyyed Abbas, Masoud Frounchi, Susan Dadbin, Sylvain Augier, Elisa Passaglia, and Francesco Ciardelli. "Modification of isotactic polypropylene by the free-radical grafting of 1,1,1-trimethylolpropane trimethacrylate." Journal of Applied Polymer Science 104, no. 2 (2007): 950–58. http://dx.doi.org/10.1002/app.25796.

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23

Rahman, Nazia, Mubarak A. Khan, Ruhul A. Khan, M. Z. I. Mollah, and Tofail A. Chowdhury. "Photocuring of Gelatin Films with TMPTMA: Effect on Aging Properties." Advanced Materials Research 123-125 (August 2010): 343–46. http://dx.doi.org/10.4028/www.scientific.net/amr.123-125.343.

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Gelatin films were prepared from granular gelatin by casting. Gelatin films were modified by photocuring with a trifunftional monomer Trimethylolpropane trimethacrylate (TMPTMA). Optimum condition for photocuring were established. Water aging of untreated and modified gelatin films was studied. Thermal aging of untreated and TMPTMA treated films were determined at different temperatures (50°C, 70°C and 100°C) for 60 min. pH aging of gelatin films were investigated in different pH solutions (3.2, 4.1, 4.8, 6.9, 9.2, 12.2) for 1min. Water aging, thermal aging and pH aging showed that the TMPTMA

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24

MATSUMOTO, Akira, Hiroyuki ANDO, and Masayoshi OIWA. "Solvent effect on the gelation in the copolymerization of methyl methacrylate with trimethylolpropane trimethacrylate." KOBUNSHI RONBUNSHU 46, no. 10 (1989): 583–89. http://dx.doi.org/10.1295/koron.46.583.

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25

Qi, Tao, Akinari Sonoda, Yoji Makita, Hirofumi Kanoh, Kenta Ooi, and Takahiro Hirotsu. "Porous properties of poly(glycidyl methacrylate-co-trimethylolpropane trimethacrylate) resins synthesized by suspension polymerization." Journal of Applied Polymer Science 83, no. 11 (2002): 2374–81. http://dx.doi.org/10.1002/app.10218.

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26

Verweij, P. D., and David C. Sherrington. "High-surface-area resins derived from 2,3-epoxypropyl methacrylate cross-linked with trimethylolpropane trimethacrylate." Journal of Materials Chemistry 1, no. 3 (1991): 371. http://dx.doi.org/10.1039/jm9910100371.

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27

Worzakowska, Marta. "Poly(trimethylolpropane trimethacrylate) modified with esters derivatives of 3-phenylprop-2-en-1-ol." Journal of Thermal Analysis and Calorimetry 132, no. 1 (2018): 225–32. http://dx.doi.org/10.1007/s10973-017-6947-3.

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28

Kitagawa, Haruaki, Kahoru Takeda, Ranna Kitagawa, et al. "Development of sustained antimicrobial-release systems using poly(2-hydroxyethyl methacrylate)/trimethylolpropane trimethacrylate hydrogels." Acta Biomaterialia 10, no. 10 (2014): 4285–95. http://dx.doi.org/10.1016/j.actbio.2014.06.016.

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29

Glad, Magnus, Per Reinholdsson, and Klaus Mosbach. "Molecularly imprinted composite polymers based on trimethylolpropane trimethacrylate (TRIM) particles for efficient enantiomeric separations." Reactive Polymers 25, no. 1 (1995): 47–54. http://dx.doi.org/10.1016/0923-1137(95)00018-e.

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30

Gama, Mariana R., Pankaj Aggarwal, Milton L. Lee, and Carla B. G. Bottoli. "Controlled crosslinking of trimethylolpropane trimethacrylate for preparation of organic monolithic columns for capillary liquid chromatography." ELECTROPHORESIS 38, no. 22-23 (2017): 3029–35. http://dx.doi.org/10.1002/elps.201700267.

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31

Adachi, Shuji, Chaiya Panintrarux, Yoichi Araki, Yukitaka Kimura та Ryuichi Matsuno. "Separation of Alkylβ-d-Glucosides andn-Alcohols by Using a Porous Trimethylolpropane Trimethacrylate Homopolymer Gel". Bioscience, Biotechnology, and Biochemistry 58, № 9 (1994): 1558–63. http://dx.doi.org/10.1271/bbb.58.1558.

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32

Rosenberg, J. E., and P. Flodin. "Macroporous gels. 3. Copolymerization of trimethylolpropane trimethacrylate and methyl methacrylate in toluene or ethyl acetate." Macromolecules 20, no. 7 (1987): 1522–26. http://dx.doi.org/10.1021/ma00173a014.

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33

Rosenberg, J. E., and P. Flodin. "Macroporous gels. 4. An NMR study of the formation of macroporous gels containing trimethylolpropane trimethacrylate." Macromolecules 21, no. 7 (1988): 2041–44. http://dx.doi.org/10.1021/ma00185a027.

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34

Walenius, Maria, Lars-Inge Kulin, and Per Flodin. "Synthesis and characterization of copolymers of trimethylolpropane trimethacrylate and glycidyl methacrylate in toluene. Part I." Reactive Polymers 17, no. 3 (1992): 309–23. http://dx.doi.org/10.1016/0923-1137(92)90277-9.

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35

Kierys, Agnieszka, Marta Grochowicz, and Patrycja Kosik. "The release of ibuprofen sodium salt from permanently porous poly(hydroxyethyl methacrylate-co-trimethylolpropane trimethacrylate) resins." Microporous and Mesoporous Materials 217 (November 2015): 133–40. http://dx.doi.org/10.1016/j.micromeso.2015.06.009.

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36

WADA, Kanae, Eri IKEDA, Junichiro WADA, Go INOUE, Munenaga MIYASAKA, and Michiyo MIYASHIN. "Wear characteristics of trimethylolpropane trimethacrylate filler-containing resins for the full crown restoration of primary molars." Dental Materials Journal 35, no. 4 (2016): 585–93. http://dx.doi.org/10.4012/dmj.2015-149.

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37

Lyamkin, D. I., S. V. Skroznikov, A. N. Zhemerikin, P. A. Cherkashin, and S. V. Cherepennikov. "The Effect of Ethylene Copolymers on the Properties of Crosslinking Polyolefin Composites Modified with Trimethylolpropane Trimethacrylate." International Polymer Science and Technology 43, no. 3 (2016): 9–12. http://dx.doi.org/10.1177/0307174x1604300302.

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38

Heinrich, Bernd, Jes Hjortkjaer, Antonios Nikitidis, and Ca rlaxel Andersson. "Poly(trimethylolpropane)trimethacrylate-bound Rh-phosphine complexes as catalysts in continuous gas-phase hydroformylation of propene." Journal of Molecular Catalysis 81, no. 3 (1993): 333–47. http://dx.doi.org/10.1016/0304-5102(93)85019-p.

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39

Fan, Pei-Ru, Xue Zhao, Ze-Hui Wei, Yan-Ping Huang, and Zhao-Sheng Liu. "Robust immobilized enzyme reactor based on trimethylolpropane trimethacrylate organic monolithic matrix through “thiol-ene” click reaction." European Polymer Journal 124 (February 2020): 109456. http://dx.doi.org/10.1016/j.eurpolymj.2019.109456.

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40

Walenius, Maria, and Per Flodin. "Reaction of the epoxide groups of the copolymer trimethylolpropane trimethacrylate-glycidyl methacrylate with aliphatic amino compounds." British Polymer Journal 23, no. 1-2 (1990): 67–70. http://dx.doi.org/10.1002/pi.4980230112.

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41

Świderska, Jolanta, Zbigniew Czech, Waldemar Świderski, and Agnieszka Kowalczyk. "Reducing of on Polymerization Shrinkage by Application of UV Curable Dental Restorative Composites." Polish Journal of Chemical Technology 16, no. 3 (2014): 51–55. http://dx.doi.org/10.2478/pjct-2014-0050.

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Abstract This manuscript describes dental compositions contain in-organic fillers, multifunctional methacrylates and photoinitiators. The main problem by application and UV curing process is the shrinkage of photoreactive dental materials during and after UV curing process. Total shrinkage of UV curable dental composites is a phenomenon of polymerization shrinkage, typical behavior for multifunctional methacrylates during polymerization process. The important factors by curing of dental composites are: kind and concentration of used methacrylates, their functionality, double bond concentration

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42

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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43

Rosenberg, J. E., and P. Flodin. "Macroporous gels. 5. A differential scanning calorimetry study of the formation of macroporous gels containing trimethylolpropane trimethacrylate." Macromolecules 22, no. 1 (1989): 155–58. http://dx.doi.org/10.1021/ma00191a030.

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44

Hjertberg, Thomas, Tihamer Hargitai, and Per Reinholdsson. "Carbon-13 CP-MAS NMR study on content and mobility of double bonds in poly(trimethylolpropane trimethacrylate)." Macromolecules 23, no. 12 (1990): 3080–87. http://dx.doi.org/10.1021/ma00214a009.

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45

Sobiech, Monika, Dorota Maciejewska, and Piotr Luliński. "Synthesis and characterization of poly(methacrylic acid-co-trimethylolpropane trimethacrylate) imprinted sorbent for analysis of biogenic amines." Materials Today Communications 22 (March 2020): 100739. http://dx.doi.org/10.1016/j.mtcomm.2019.100739.

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46

Courtois, Julien, Gerd Fischer, Börje Sellergren, and Knut Irgum. "Molecularly imprinted polymers grafted to flow through poly(trimethylolpropane trimethacrylate) monoliths for capillary-based solid-phase extraction." Journal of Chromatography A 1109, no. 1 (2006): 92–99. http://dx.doi.org/10.1016/j.chroma.2005.12.014.

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47

Reinholdsson, Per, Antonios Nikitidis, and Carlaxel Andersson. "Poly(trimethylolpropane trimethacrylate) particles with phosphine functionality. A new type of support for metal phosphine complex catalysts." Reactive Polymers 17, no. 2 (1992): 187–95. http://dx.doi.org/10.1016/0923-1137(92)90151-q.

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48

Yu, Jin Yang, Xiao Ling Hu, Ren Yuan Song, and Shan Xi. "Molecularly Imprinted Polymer Microspheres Prepared by Precipitation Polymerization for Atenolol Recognition." Advanced Materials Research 148-149 (October 2010): 1192–98. http://dx.doi.org/10.4028/www.scientific.net/amr.148-149.1192.

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Molecularly imprinted polymer microspheres for selective binding and recognition of atenolol were prepared by means of precipitation polymerization method using methacylic acid as functional monomer and trimethylolpropane trimethacrylate as cross-linker in the presence of atenolol as template molecule in acetonitrile solution. Computer simulation was employed to demonstrate the mechanism of the interaction between methacylic acid and atenolol. The scanning electron microscopy exhibited that the polymers were uniform spheres with the diameter of about 0.6µm. The adsorption properties of atenolo

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49

Datta, Sujit K., Tapan K. Chaki, and Anil K. Bhowmick. "Electron Beam Initiated Grafting and Crosslinking of Ethylene Vinyl Acetate Copolymer. Part-I: Structural Characterization." Rubber Chemistry and Technology 69, no. 1 (1996): 120–29. http://dx.doi.org/10.5254/1.3538352.

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Abstract Electron beam irradiation of Ethylene vinyl acetate, EVA (VA content 12, 28 & 45%) copolymer was carried out in presence of trimethylolpropane trimethacrylate (TMPTMA) and triallyl cyanurate (TAC) and the structure of the modified copolymers was determined with the help of IR spectroscopy and gel content measurements. The IR absorbance peak at 1640 cm−1 disappears at lower radiation dose indicating that the grafting and crosslinking reactions take place through double bonds. Some carbonyl groups are formed during irradiation. The concentration of carbonyl group increases with the

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50

Czulak, Joanna, Anna Jakubiak-Marcinkowska, and Andrzej Trochimczuk. "Polymer Catalysts Imprinted with Metal Ions as Biomimics of Metalloenzymes." Advances in Materials Science and Engineering 2013 (2013): 1–9. http://dx.doi.org/10.1155/2013/464265.

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This work presents the preparation and properties of molecularly imprinted polymers (MIPs) with catalytic centers that mimic the active sites of metalloenzymes. The MIP synthesis was based on suspension polymerization of functional monomers (4-vinylpyridine and acrylonitrile) with trimethylolpropane trimethacrylate as a crosslinker in the presence of transition metal ions and 4-methoxybenzyl alcohol as a template. Four metal ions have been chosen for imprinting from among the microelements that are the most essential in the native enzymes: Cu2+, Co2+, Mn2+, and Zn2+. To prepare catalysts, the

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