Polymerization of Lactams (IX). Anionic Polymerization of 2-Pyrrolidone via Phenylphosphonyl-N,N'-bis-${\varepsilon}$-caprolactam / KOH Catalysis

Lactam의 중합 (제9보). Phenylphosphonyl-N,N'-bis-${\varepsilon}$-caprolactam / KOH 촉매작용에 의한 2-Pyrrolidone 의 음이온 중합

  • Jung Hag Park (Department of Chemistry, Korea Advanced Institute of Science) ;
  • Bal Jung (Department of Chemistry, Korea Advanced Institute of Science) ;
  • Sam K. Choi (Department of Chemistry, Korea Advanced Institute of Science)
  • Published : 1980.04.30

Abstract

Anionic polymerization of 2-pyrrolidone was carried out via PPBC/KOH catalysis. The effects of PPBC/KOH mole ratio, KOH concentration and temperature on polymerization have been investigated. It was observed that the highest rate of polymerization and maximum conversion were obtained when PPBC/KOH mole ratio was around 0.5. The maximum conversion and the highest viscosity were obtained when the concentration of KOH was 2 mole percent. It was also found that while the rate of polymerization at $50^{\circ}C$ was higher than at $30^{\circ}C$ in the initial stage of polymerization, the conversion and viscosity were decreased as polymerization time was extended. The rate constant $(k_p)$ of polymerization was determined by least square method; the values of $k_p$ obtained were $22.4\;l/mole{\cdot}hr\;at\;30^{\circ}C\;and\;191.9\;l/mole{\cdot}hr\;at\;50^{\circ}C$, respectively.

PPBC/KOH 촉매작용에 의한 2-pyrrolidone의 음이온중합에 있어서 PPBC/KOH 몰비, KOH의 농도 및 온도가 중합에 미치는 영향을 조사하였다. PPBC/KOH 몰비가 0.5일때 중합속도가 가장 빠르고 전환율도 가장 높았으며, 또 KOH 의 농도는 2몰%일때 가장 높은 전환율과 점도가 얻어졌다. $50^{\circ}C$에서의 중합은 $30^{\circ}C$에서의 중합보다 초기반응속도는 빠르나 시간이 경과할 수록 전환율과 점도가 오히려 낮아지는 경향이 관찰되었다. 최소자승법으로 계산하여 구한 중합속도상수$(k_p)$의 값은 $30^{\circ}C$일때 $22.4\;l/mole{\cdot}hr$ 였고 $50^{\circ}C$일때 $191.9\;l/mole{\cdot}hr$ 였다.

Keywords

References

  1. U. S. Pat., 2638463, v.4 W. O. Ney, Jr.;W. R. Nummy;C. E. Barnes
  2. U. S. Pat., 2739959 v.50 W. O. Ney, Jr.;M. Crowther
  3. Brit. Pat., 754944 v.51 A. Hoffmann
  4. U. S. Pat., 2809958 v.52 C. E. Barnes;W. O. Ney, Jr;W. R. Nummy
  5. Bull. Soc. Chim. France H. Sekiguchi
  6. J. Korean Chem. Soc. v.20 B. Jung;S. K. Choi;G. S. Seo
  7. J. Korean Chem. Soc. v.20 H. K. Shu;S. K. Choi
  8. J. Korean Chem. Soc. v.21 G. S. Suh;S. K. Choi
  9. J. Korean Chem. Soc. v.21 M. S. Koo;S. K. Choi
  10. Polymer (Korea) J. K. Yoo;S. K. Choi
  11. J. Korean Chem. Soc. W. J. Jung;S. K. Choi
  12. J. Korean Chem. Soc. Y. W. Park;S. K. Choi
  13. Polymer (Korea) H. B. Kim;S. K. Choi
  14. J. Polym. Sci., Polym. Chem. Ed. v.15 S. W. Shalaby;H. K. Reimschuessel
  15. Collect. Czech. Chem. Commun. v.39 Z. Tuzar;J. Kleteckova;J. Kralicek
  16. J. Polym. Sci. v.3 S. Barzakay;M. Levy;D. Vefsi
  17. J. Polym. Sci. v.4 S. Barzakay;M. Levy;D. Vefsi
  18. J. Polym. Sci. v.5 S. Barzakay;M. Levy;D. Vefsi