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DBU-intercalated γ-titanium phosphate as a latent thermal catalyst in the reaction of glycidyl phenyl ether (GPE) and hexahydro-4-methylphthalic anhydride (MHHPA).
Fujiwara, Ayumi; Furuya, Hiroshi; Mamun Kabir, Shekh Md; Shizuma, Motohiro; Ohtaka, Atsushi; Shimomura, Osamu.
Afiliação
  • Fujiwara A; Department of Applied Chemistry, Osaka Institute of Technology 5-16-1 Omiya, Ashahi-ku Osaka 535-8585 Japan osamu.shimomura@oit.ac.jp.
  • Furuya H; Department of Applied Chemistry, Osaka Institute of Technology 5-16-1 Omiya, Ashahi-ku Osaka 535-8585 Japan osamu.shimomura@oit.ac.jp.
  • Mamun Kabir SM; Department of Applied Chemistry, Osaka Institute of Technology 5-16-1 Omiya, Ashahi-ku Osaka 535-8585 Japan osamu.shimomura@oit.ac.jp.
  • Shizuma M; Department of Wet Process Engineering, Bangladesh University of Textiles Tejgaon Dhaka-1208 Bangladesh.
  • Ohtaka A; Osaka Research Institute of Industrial Science and Technology 1-6-50 Morinomiya, Joto-ku Osaka 536-8553 Japan.
  • Shimomura O; Department of Applied Chemistry, Osaka Institute of Technology 5-16-1 Omiya, Ashahi-ku Osaka 535-8585 Japan osamu.shimomura@oit.ac.jp.
RSC Adv ; 13(13): 8630-8635, 2023 Mar 14.
Article em En | MEDLINE | ID: mdl-36936818
The capabilities and performance of γ-titanium phosphate (γ-TiP) with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) as a latent thermal catalyst were investigated by the copolymerization of glycidyl phenyl ether (GPE) and hexahydro-4-methylphthalic anhydride (MHHPA) at different temperatures for a period of one hour. Polymerization was not observed until the reactants were heated to 100 °C. Upon increasing the temperature to 120 °C, the conversion in the presence of γ-TiP·DBU as a catalyst showed 98% conversion in 1 h. The thermal stability of GPE and MHHPA reacted in the presence of γ-TiP·DBU at 40 °C for 144 h resulted in less than 7% conversion of GPE. The conversion of GPE did not show a significant increase at 40 °C.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: RSC Adv Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: RSC Adv Ano de publicação: 2023 Tipo de documento: Article