Article
  • Ultrasonic Degradation of Poly(Styrene-co-divinylbenzene) Macrogel
  • Jeong SY, Kim KS, Kim YJ, Park MH, Chung KH
  • Poly(styrene-co-divinylbenzene) Macrogel의 초음파 분해
  • 정승영, 김공수, 김영준, 박명환, 정기현
Abstract
Poly(styrene-co-divinylbenzene) macrogels were synthesized by varing the volume fractions of solvents and mole ratios of monomers. Weight swelling degree and molecular weight per crosslinked unit of the macrogels were determined. The macrogels were degraded by ultrasonic degradation for 9∼ 84 hours, and the obtained macrogels were characterized by gel permeation chromatography and viscometry. As ultrasonic degradation time increased, largo size particles with low crosslinked density were degraded preferentially, compared with small size particles having high crosslinked density. GPC profiles of the obtained macrogels were shifted to low molecular weight region and approached elution count 19.43(Mw=1.60×105) with degradation time.

Styrene과 divinylbenzene의 몰비와 용매의 체적비를 변화시키면서 poly(styrene-co-divinyl-benzene) macrogel을 합성하여 합성한 macrogel의 중량 팽윤도, 가교점간 분자량등을 측정하였다. 또한, macrogel을 9∼84시간 동안 초음파 분해하였다. 초음파 분해하여 얻어진 macrogel의 특성을 gel permeation chromatography및 점도측정을 통하여 고찰하였다. 초음파 분해시간이 증가할수록 고 가교밀도를 갖는 작은 크기의 입자에 비해 저 가교밀도를 갖는 큰 크기의 입자들이 우선적으로 절단되었고, GPC profile이 저 분자량 쪽으로 이동하였으며, 본 실험조건의 절단 한계치인 elution count 19.43(Mw=1.60×105)에 수렴하였다.

References
  • 1. Mostafa MA, J. Polym. Sci., 28, 519 (1958)
  •  
  • 2. Jellinek HH, J. Polym. Sci., 37, 485 (1959)
  •  
  • 3. Mostafa MA, J. Polym. Sci., 33, 311 (1958)
  •  
  • 4. Jellinek HH, Brett HW, J. Polym. Sci., 21, 535 (1956)
  •  
  • 5. Schmid G, Beuttenmuller E, Z. Elektrochem., 49(4-5), 325 (1943)
  •  
  • 6. Basedow AM, Ebert KH, Makromol. Chem., 176, 745 (1975)
  •  
  • 7. Alexander P, Fox M, J. Polym. Sci., 12, 533 (1954)
  •  
  • 8. Jellinek HH, J. Polym. Sci., 22, 149 (1956)
  •  
  • 9. Okuyama M, Z. Elektrochem., 59(16), 565 (1955)
  •  
  • 10. Collins EA, Bares J, Billmeyer FWExperiments in Polymer Science, p. 306, John Wiley & Sons, Inc., Canada (1973)
  •  
  • 11. Boundy RH, Boyer RFStyrene, Its Polymers, Copolymers and Derivatives, Reinhold Publishing Corp., New York (1952)
  •  
  • 12. Schmid G, Rommel O, J. Phys. Chem., 185, 97 (1939)
  •  
  • 13. Schmid G, Paret G, Pfleiderer H, Kolloid Z., 124, 150 (1951)
  •  
  • 14. Schmid G, Beuttenmuller E, Z. Elektrochem., 50(9-10), 209 (1944)
  •  
  • 15. Melville HW, Murray AJR, Trans. Far. Soc., 46, 996 (1950)
  •  
  • 16. Huggins ML, J. Phys. Chem., 42, 911 (1938)
  •  
  • 17. Huggins ML, J. Phys. Chem., 43, 439 (1939)
  •  
  • 18. Kirkwood JG, Riseman J, J. Chem. Phys., 16, 565 (1948)
  •  
  • 19. Auer PL, Gardner CS, J. Chem. Phys., 23, 1546 (1955)
  •  
  • 20. Einstein A, Ann. Phys., 19, 289 (1906)
  •  
  • 21. Einstein A, Ann. Phys., 34, 591 (1911)
  •  
  • 22. Stockmayer WH, Fixman M, Ann. N.Y. Aoad. Sci., 57, 334 (1953)
  •  
  • 23. Grubisic Z, Rempp P, Benoit H, J. Polym. Sci. B: Polym. Phys., 5, 753 (1967)
  •  
  • Polymer(Korea) 폴리머
  • Frequency : Bimonthly(odd)
    ISSN 0379-153X(Print)
    ISSN 2234-8077(Online)
    Abbr. Polym. Korea
  • 2022 Impact Factor : 0.4
  • Indexed in SCIE

This Article

  • 1992; 16(2): 138-144

    Published online Mar 25, 1992