SWELLING BEHAVIOR OF RUBBER VULCANIZATES .1. REAL-TIME PULSED NUCLEAR-MAGNETIC-RESONANCE MEASUREMENTS

被引:17
作者
FUKUMORI, K
KURAUCHI, T
KAMIGAITO, O
机构
[1] Toyota Central Research and Development Laboratories, Inc., Aichi-gun, Aichi-ken, 480-11, 41-1, Nagakute-cho
关键词
!sup]1[!/sup]H pulsed n.m.r; carbon black; molecular mobility; real-time measurement; rubber vulcanizate; spin-spin relaxation time; swelling;
D O I
10.1016/0032-3861(90)90294-9
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Swelling behaviour of acrylonitrile-butadiene copolymer rubber vulcanizates immersed in a nonprotonic solvent was studied by real-time pulsed nuclear magnetic resonance (n.m.r.) measurements. The temporal change of the proton spin-spin relaxation time, T2, during the swelling process was obtained. The T2 signal for the rubber vulcanizates was resolved into two exponentially decaying components (short T2 and long T2). The short T2 component is assigned to the constrained regions in the rubber matrix, which may be mainly located around the crosslinks, and the long T2 component to the regions lying outside the constraints. It was suggested that the decreased change of the fraction of the short T2 component by swelling is closely connected with the enhanced molecular mobility of the network chains between the adjacent crosslinks through the diffusion of the solvent. The restricted swelling behaviour of the carbon black-filled rubber vulcanizates was interpreted mainly in terms of the constrained molecular motions of the network chains through the rubber-filler interactions and spatial effects of the filler particles. It becomes clear that the real-time pulsed n.m.r. measurements complement the results of the macroscopic swelling measurements for the rubber vulcanizates with more detailed information on the molecular interactions between the rubber and solvent molecules. © 1990.
引用
收藏
页码:713 / 720
页数:8
相关论文
共 36 条
[1]   ELASTOMER GASOLINE BLENDS INTERACTIONS .1. EFFECTS OF METHANOL GASOLINE MIXTURES ON ELASTOMERS [J].
ABUISA, IA .
RUBBER CHEMISTRY AND TECHNOLOGY, 1983, 56 (01) :135-168
[2]  
[Anonymous], 1980, VISCOELASTIC PROPERT
[3]   A DIFFUSIVITY APPROACH FOR STUDYING POLYMER STRUCTURE [J].
AUERBACH, I ;
MILLER, WR ;
KURYLA, WC ;
GEHMAN, SD .
JOURNAL OF POLYMER SCIENCE, 1958, 28 (116) :129-150
[4]   SOME COMMENTS ON THE SWELLING OF POLYMERIC NETWORKS IN RELATION TO THEIR STRUCTURE [J].
BASTIDE, J ;
PICOT, C ;
CANDAU, S .
JOURNAL OF MACROMOLECULAR SCIENCE-PHYSICS, 1981, B19 (01) :13-34
[5]   RELAXATION EFFECTS IN NUCLEAR MAGNETIC RESONANCE ABSORPTION [J].
BLOEMBERGEN, N ;
PURCELL, EM ;
POUND, RV .
PHYSICAL REVIEW, 1948, 73 (07) :679-712
[6]  
Boonstra B, 1965, RUBBER CHEM TECHNOL, V38, P943, DOI DOI 10.5254/1.3535712
[7]   DIFFUSION OF HEAVY OIL IN A SWELLING ELASTOMER [J].
BOUVIER, JM ;
GELUS, M .
RUBBER CHEMISTRY AND TECHNOLOGY, 1986, 59 (02) :233-240
[8]   ENTANGLEMENTS AND ELASTICITY IN POLYBUTADIENE NETWORKS [J].
BROWN, DR ;
MUNIE, GC ;
JONAS, J .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1982, 20 (09) :1659-1668
[9]  
BROWN RP, 1986, PHYSICAL TESTING RUB, P283
[10]   NMR OBSERVATION OF THE SWELLING PROCESS OF POLYDIMETHYLSILOXANE NETWORKS - AVERAGE ORIENTATIONAL ORDER OF MONOMERIC UNITS [J].
COHENADDAD, JP ;
DOMARD, M ;
HERZ, J .
JOURNAL OF CHEMICAL PHYSICS, 1982, 76 (05) :2744-2753