Tytuł artykułu
Autorzy
Wybrane pełne teksty z tego czasopisma
Identyfikatory
Warianty tytułu
Języki publikacji
Abstrakty
The acrylate monomer was synthesized by two step process. 2,4-dichloro-1-ene(4-hydroxyphenyl)phenone (DHP) was synthesized using 4-hydroxy benzaldehyde and 2,4-dichloro acetophenone. 4-[3-(2,4-dichloro-phenyl)3-oxoprop-1-en-1-yl]phenylacrylate (DCP) was prepared by reacting DHP with acryloyl chloride. The synthesized monomer was copolymerized with 2-hydroxyethyl acrylate and styrene using solution polymerization technique. Monomer and polymers were characterized by IR, NMR and UV techniques. The average molecular weight of the polymer was around 4000 g/mol. First and second decomposition temperature of the polymers was around 320 °C and 430 °C, respectively. The reactivity ratio of the polymers was calculated by Fineman-Ross, Kelen-Tudos and extended Kelen-Tudos methods. The synthesized monomer has been less reactive than the commercial monomer. The rate of photocrosslinking increased from 39 % to 99 % due to the using of copolymerization technique.
Słowa kluczowe
Wydawca
Czasopismo
Rocznik
Tom
Strony
834--844
Opis fizyczny
Bibliogr. 25 poz., rys., tab.
Twórcy
autor
- PG & Research Department of Chemistry, Government Arts College, Thiruvannamalai-606603. Tamilnadu, India.
autor
- PG & Research Department of Chemistry, Government Arts College, Thiruvannamalai-606603. Tamilnadu, India.
autor
- PG & Research Department of Chemistry, Government Arts College, Thiruvannamalai-606603. Tamilnadu, India.
Bibliografia
- [1] REHAB A., SALAHUDDIN N., Polymer, 40 (1999), 2197.
- [2] KAWATZWKI N., YAMANOTO T., ONO H., Appl. Phys. Lett., 74 (1999), 935.
- [3] QI Y.H., DING J.F., MICHAEL D., JIA J., CALLENDER C.L., Polymer, 47 (2006), 8263.
- [4] CHEN H., YIN J., J. Polym. Sci. Pol. Chem., 42 (2004), 1735.
- [5] LI X.D., ZHONG Z.X., JIN G., LEE S.H., LEE M.H., Macromol. Res., 14 (2006), 257.
- [6] OHE Y., ITO H., WATANABE N., ICHIMURA K., J. Appl. Polym. Sci., 77 (2000), 2189.
- [7] PRIYAREGA S., MUTHUSAMY A., KANIAPPAN K., MURUGAVEL S.C., Des. Monomers Polym., 6 (2003), 187.
- [8] SUBRAMANIAN K., KRISHNASAMY V., NANJUNDAN S., RAMI REDDY A.V., Eur. Polym. J., 36 (2000), 2343.
- [9] BALAJI R., NANJUNDAN S., React. Funct. Polym., 49 (2001), 77.
- [10] NISHIKUBO T., KAMEYAMA A., TSUTSUI K., J. Polym. Sci. Polym. Chem., 39 (2001), 1169.
- [11] PERNY S., BARNY P.L., DELAIRE J., DOZOV I., FORGET S., AUROY P., Liq. Cryst., 27 (2000), 349.
- [12] SUBRAMANIAN K., KRISHNASAMY V., NANJUNDAN S., RAMI REDDY A.V., Eur. Polym. J., 36 (2000), 2343.
- [13] PERNY S., BARNY P.L., DELAIRE J., BUFFETEAN T., SOURISSEAN C., DOZOV I., FORGET S., MARTIENLGARDE P., Liq. Cryst., 27 (2000), 329.
- [14] XU J., RONG X., CHI T., WANG M., WANG Y., YANG D., QIU F., J. Appl. Polym. Sci., 130 (2013), 3142.
- [15] SHIRAI M., Polym. J., 46 (2014), 859.
- [16] ARUN A., REDDY B.S.R., J. Polym. Sci. Polym. Chem., 41 (2003), 1632.
- [17] ARUN A., REDDY B.S.R., J. Polym. Sci. Polym. Chem., 42 (2004), 3433.
- [18] STAMPEL G.M., CROSS R.P., MALLIELLA R.P., J. Am. Chem. Soc., 72 (1950), 2899.
- [19] SURESH J., VAKEES E., KARTHIK S., KAYALVIZHI M., ARUN A., Des. Monomers Polym., 17 (2014), 753.
- [20] ARUN A., REDDY B.S.R., Eur. Polym. J., 40 (2004), 589.
- [21] ESQUIVEL-GUZMAN ´ J.A., ZARAGOZA-GALAN ´ G., ORT´ IZ-PALACIOS J., RIVERA E., Des. Monomers Polym., 15 (2012), 561.
- [22] VIJAYANAND P.S., KATO S., KOYAMA M., SATOKAWA S., KOJIMA T., Des. Monomers Polym., 10 (2007), 375.
- [23] NISHIKUBO T., IIZAWA T., TAKAHASHI E., FUMIHIKO N., Macromolecules, 18 (1985), 2131.
- [24] LAMAITRE E., COQUERET K., MERUIER R., COMBIER A.L., LOUCHEUX C., J. Appl. Polym. Sci., 33 (1987), 2189.
- [25] RAMI REDDY A.V., SUBRAMANIAN K., SESHA SAINATH A.V., J. Appl. Polym. Sci., 70 (1998), 2111.
Uwagi
Opracowanie ze środków MNiSW w ramach umowy 812/P-DUN/2016 na działalność upowszechniającą naukę (zadania 2017).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-d387292d-2683-4f74-9893-4f07b6262aa5