POLYMORPHISM IN SYNDIOTACTIC POLYSTYRENE - A H-1-NMR RELAXATION STUDY

被引:52
作者
CAPITANI, D
DEROSA, C
FERRANDO, A
GRASSI, A
SEGRE, AL
机构
[1] CNR,IST STRUTTURIST CHIM G GIACOMELLO,MB 10,MONTEROTONDO STN,I-00016 ROME,ITALY
[2] MONTEDIPE SPA,I-46100 MANTOVA,ITALY
[3] SALERNO UNIV,DEPT PHYS,I-84081 SALERNO,ITALY
[4] NAPLES UNIV,DEPT CHEM,I-80134 NAPLES,ITALY
关键词
D O I
10.1021/ma00041a008
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A marked shortening of T, relaxations in solid aromatic polymers can be attributed to O2 adsorbed on the aromatic rings. This effect, observed as a function of temperature, is modulated by the amount of adsorbed O2, Which, in turn, varies according to the molecular packing and crystalline/amorphous ratio. Within the temperature range 77-400 K, semicrystalline syndiotactic polystyrenes (s-PS) in the alpha, beta, and gamma-polymorph modifications were studied by pulse H-1 NMR at 30 MHz. Due to the presence of many relaxation components, 1,2,2-trideuterio-s-PS was synthesized, crystallized, and characterized by X-ray powder diffraction. At low temperature, when both the O2 diffusion and the spin-diffusion processes are slow enough, the backbone-deuteriated polymers exhibit multiple T1 relaxations: three for alpha and beta s-PS and two for gamma s-PS. These T1 components are attributed to crystalline and amorphous phases. From the study of these components as a function of temperature and from direct comparison of T1 values in the different phases, the following conclusions were drawn: (i) Clear differentiation was possible between different s-PS polymorphs. (ii) Determination of the crystalline vs amorphous ratio fully consistent with X-ray diffraction data was achieved. (iii) The amorphous component of different semicrystalline s-PS polymorphs could be distinguished.
引用
收藏
页码:3874 / 3880
页数:7
相关论文
共 35 条
  • [1] [Anonymous], 1966, INTRO SOLID STATE PH
  • [2] [Anonymous], 1988, NUMERICAL RECIPES AR
  • [3] PULSED H-1-NMR RELAXATION IN CRYSTALLINE SYNDIOTACTIC POLYSTYRENE
    CAPITANI, D
    SEGRE, AL
    GRASSI, A
    SYKORA, S
    [J]. MACROMOLECULES, 1991, 24 (02) : 623 - 624
  • [4] CHATANI Y, 1988, POLYM PREPR JPN, V37, pE428
  • [5] DINOLA A, COMMUNICATION
  • [6] ERNST RR, 1987, PRINCIPLES NUCLEAR M, pCH4
  • [7] NMR RELAXATION-TIME STUDIES OF POLYSTYRENE
    FROIX, MF
    WILLIAMS, DJ
    GOEDDE, AO
    [J]. MACROMOLECULES, 1976, 9 (02) : 354 - 358
  • [8] Fukushima E., 1981, EXPT PULSE NMR NUTS
  • [9] C-13 NUCLEAR-MAGNETIC-RESONANCE STUDY OF CHAIN CONFORMATION IN THE SOLID POLYMORPHS OF SYNDIOTACTIC POLYSTYRENE
    GOMEZ, MA
    TONELLI, AE
    [J]. MACROMOLECULES, 1990, 23 (13) : 3385 - 3386
  • [10] GRASSI A, 1989, MAKROMOL CHEM-RAPID, V10, P687