Solid state 13C NMR study of the char forming processes in polychloroprene

被引:27
作者
Dick, CM
Liggat, JJ
Snape, CE
机构
[1] Univ Strathclyde, Dept Pure & Appl Chem, Glasgow G1 1XL, Lanark, Scotland
[2] Univ Nottingham, Sch Chem Environm & Min Engn, Nottingham NG7 2RD, England
关键词
polychloroprene; thermal degradation; char formation; solid state C-13 NMR; DSC; TGA;
D O I
10.1016/S0141-3910(01)00174-4
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理]; 080501 [材料物理与化学]; 081704 [应用化学];
摘要
Polychloroprene, also known as neoprene, is an elastomer commonly utilised in the electrical and automobile industries. Its degradation is known to occur predominantly in a two stage process: HCl is lost in the initial step, whilst the second step involves the production of volatile hydrocarbons through chain scission. In this paper we describe the use of solid state C-13 NMR as a probe for structural changes in the condensed phase during these degradative steps. Cross polarisation-magic angle spinning (CP-MAS) analysis of virgin polychloroprene and a series of samples degraded at temperatures between 275 and 550 degreesC reveals that as degradation becomes more advanced there is a steady loss of sp(3) carbon with a commensurate growth in sp(2) carbon. The bulk of the chlorine loss occurs by 350 degreesC with the aliphatic carbon lost by 550 degreesC, by which temperature the residue is essentially aromatic carbon. Dipolar dephasing experiments show that this residue is essentially a network of, on average, tri-substituted phenyl rings. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:397 / 405
页数:9
相关论文
共 29 条
[1]
BAILEY HC, 1964, POLYMER PREPRINTS, V5, P525
[2]
Synergistic effect of zeolite in an intumescence process - Study of the interactions between the polymer and the additives [J].
Bourbigot, S ;
LeBras, M ;
Delobel, R ;
Tremillon, JM .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1996, 92 (18) :3435-3444
[3]
Synergistic effect of zeolite in an intumescence process: Study of the carbonaceous structures using solid-state NMR [J].
Bourbigot, S ;
LeBras, M ;
Delobel, R ;
Decressain, R ;
Amoureux, JP .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1996, 92 (01) :149-158
[4]
APPLICATION OF INFRA-RED DIGITAL SUBTRACTION TECHNIQUES TO THE MICROSTRUCTURE OF POLYCHLOROPRENES .1. ACCENTUATION AND ASSIGNMENT OF BANDS DUE TO STRUCTURAL IRREGULARITIES [J].
COLEMAN, MM ;
PETCAVICH, RJ ;
PAINTER, PC .
POLYMER, 1978, 19 (11) :1243-1248
[5]
Cullis C. F., 1981, COMBUSTION ORGANIC P
[6]
The flammability of urethane-modified polyisocyanurates and its relationship to thermal degradation chemistry [J].
Dick, C ;
Dominguez-Rosado, E ;
Eling, B ;
Liggat, JJ ;
Lindsay, CI ;
Martin, SC ;
Mohammed, MH ;
Seeley, G ;
Snape, CE .
POLYMER, 2001, 42 (03) :913-923
[7]
Dick CM, 2000, POLYM INT, V49, P1177, DOI 10.1002/1097-0126(200010)49:10<1177::AID-PI437>3.0.CO
[8]
2-5
[9]
MEASUREMENT OF C-13 CHEMICAL-SHIFTS IN SOLIDS [J].
EARL, WL ;
VANDERHART, DL .
JOURNAL OF MAGNETIC RESONANCE, 1982, 48 (01) :35-54
[10]
THERMAL DEGRADATION OF POLYCHLOROPRENE .1. THERMAL ANALYSIS STUDIES OF STABILITY OF POLYCHLOROPRENE SAMPLES, AND MEASUREMENTS OF KINETICS OF DEGRADATION [J].
GARDNER, DL ;
MCNEILL, IC .
EUROPEAN POLYMER JOURNAL, 1971, 7 (06) :569-&