Crystallization and Stress Relaxation in Highly Stretched Samples of Natural Rubber and Its Synthetic Analogue. Volume 39, Number 15, July 25, 2006, pp 5100−5105.

2006 ◽  
Vol 39 (19) ◽  
pp. 6784-6784 ◽  
Author(s):  
M. Tosaka ◽  
D. Kawakami ◽  
K. Senoo ◽  
S. Kohjiya ◽  
Y. Ikeda ◽  
...  
Keyword(s):  
Stress Relaxation ◽  
Natural Rubber ◽  
Synthetic Analogue

Crystallization and Stress Relaxation in Highly Stretched Samples of Natural Rubber and Its Synthetic Analogue

2006 ◽  
Vol 39 (15) ◽  
pp. 5100-5105 ◽  
Author(s):  
Masatoshi Tosaka ◽  
Daisuke Kawakami ◽  
Kazunobu Senoo ◽  
Shinzo Kohjiya ◽  
Yuko Ikeda ◽  
...  
Keyword(s):  
Stress Relaxation ◽  
Natural Rubber ◽  
Synthetic Analogue

Effects of accelerator type on stress relaxation behavior and network structure of aged natural rubber/chloroprene rubber vulcanizates

2016 ◽  
Vol 49 (5) ◽  
pp. 381-396 ◽  
Author(s):  
Farzad A Nobari Azar ◽  
Murat Şen
Keyword(s):  
Stress Relaxation ◽  
Natural Rubber ◽  
Network Structure ◽  
Structural Changes ◽  
Relaxation Behavior ◽  
Stress Relaxation Behavior ◽  
Rubber Blends ◽  
Chloroprene Rubber ◽  
Weather Changes ◽  
Behavior Network

Natural rubber/chloroprene rubber (NR/CR) blends are among the commonly used rubber blends in industry and continuously are exposed to severe weather changes. To investigate the effects of accelerator type on the network structure and stress relaxation of unaged and aged NR/CE vulcanizates, tetramethyl thiuram disulfide, 2-mercaptobenzothiazole, and diphenyl guanidine accelerators have been chosen to represent fast, moderate, and slow accelerator groups, respectively. Three batches have been prepared with exactly the same components and mixing conditions differing only in accelerator type. Temperatures scanning stress relaxation and pulse nuclear magnetic resonance techniques have been used to reveal the structural changes of differently accelerated rubber blends before and after weathering. Nonoxidative thermal decomposition analyses have been carried out using a thermogravimetric analyzer. Results indicate that there is a strong interdependence between accelerator type and stress relaxation behavior, network structure, cross-linking density, and aging behavior of the blends. Accelerator type also affects decomposition energy of the blends.

Aging of Natural Rubber Vulcanizates in the Presence of Dithiocarbamates

1959 ◽  
Vol 32 (3) ◽  
pp. 739-747 ◽  
Author(s):  
J. R. Dunn ◽  
J. Scanlan
Keyword(s):  
Stress Relaxation ◽  
Natural Rubber ◽  
Protective Action ◽  
Dicumyl Peroxide ◽  
Vulcanized Rubber ◽  
Aging Properties ◽  
Photochemical Aging ◽  
Natural Rubber Vulcanizates

Abstract The thermal and photochemical aging of extracted dicumyl peroxide-, TMTD (sulfurless)- and santocure-vulcanized rubber, in presence of a number of metal and alkylammonium dithiocarbamates, has been investigated by measurements of stress relaxation. The dithiocarbamates have a considerable protective action upon the degradation of peroxide- and TMTD-vulcanizates, but they accelerate stress decay in santocure-accelerated vulcanizates. The reasons for this behavior are discussed. It is suggested that the excellent aging properties of unextracted TMTD vulcanizates are due to the presence of zinc dimethyldithiocarbamate formed during vulcanization.

Stress relaxation of natural rubber during irradiation

1969 ◽  
Vol 7 (4) ◽  
pp. 725-733 ◽  
Author(s):  
D. Evans ◽  
J. T. Morgan ◽  
R. Sheldon ◽  
G. B. Stapleton
Keyword(s):  
Stress Relaxation ◽  
Natural Rubber

Longitudinal Cracking in a Carbon Black Filled Natural Rubber Vulcanizate during Chemical Stress Relaxation

1998 ◽  
Vol 71 (2) ◽  
pp. 157-167 ◽  
Author(s):  
G. R. Hamed ◽  
J. Zhao
Keyword(s):  
Stress Relaxation ◽  
Carbon Black ◽  
Natural Rubber ◽  
Longitudinal Crack ◽  
Chemical Stress ◽  
Loading Direction ◽  
Rubber Vulcanizate ◽  
Edge Cracks ◽  
Forced Air ◽  
Oxidative Attack

Abstract Thin specimens of a black-filled, natural rubber vulcanizate have been held in uniaxial tension at 72°C and 200% elongation in a forced air oven. After substantial oxidative attack (inferred from stress relaxation), small edge cracks formed. Initially, these cracks grew perpendicular to the loading direction, but, upon reaching about 0.1 mm in depth, longitudinal crack growth commenced and fracture progressed by a kind of 0°-peel process with “splitting-off” of successive strands of rubber. This phenomenon is attributed to anisotropy in strength caused both by straining and by oxidative attack.

Relaxation Processes in the Deformation of Unloaded Rubbers and the Influence of the Degree of Vulcanization

1951 ◽  
Vol 24 (4) ◽  
pp. 810-819
Author(s):  
B. A. Dogadkin ◽  
M. M. Reznikovskii˘
Keyword(s):  
Stress Relaxation ◽  
Natural Rubber ◽  
Elastic Deformation ◽  
Relaxation Processes ◽  
Spatial Network ◽  
Relaxation Properties ◽  
Constant Rate ◽  
Different Temperatures ◽  
Kinetics Of

Abstract 1. It is shown that the process of stress relaxation at different initial elongations as well as the process of deformation at constant rate for unloaded rubbers at different temperatures (20–70° C) can be represented quantitatively by equations suggested in earlier works. Likewise the possibility of expanding the theories proposed for the kinetics of high-elastic deformation of spatial polymers is substantiated. 2. It is shown that the relaxation properties of soft unloaded vulcanizates of natural rubber and many synthetic rubbers do not undergo essential changes during vulcanization. 3. The conjecture is expressed that the invariability of the relaxation properties during vulcanization continues until the bonds of the spatial network are distributed sufficiently widely not to influence the activity or heat movement of the chain segments between them.

DEPENDENCE OF THE ONSET OF STRAIN-INDUCED CRYSTALLIZATION OF NATURAL RUBBER AND ITS SYNTHETIC ANALOGUE ON CROSSLINK AND ENTANGLEMENT BY USING SYNCHROTRON X-RAY

2017 ◽  
Vol 90 (4) ◽  
pp. 728-742 ◽  
Author(s):  
Watcharin Sainumsai ◽  
Shigeyuki Toki ◽  
Sureerut Amnuaypornsri ◽  
Adun Nimpaiboon ◽  
Jitladda Sakdapipanich ◽  
...  
Keyword(s):  
Natural Rubber ◽  
Crosslink Density ◽  
Inhomogeneous Material ◽  
Synthetic Analogue ◽  
Stress Strain ◽  
X Ray ◽  
Stress Strain Relation ◽  
Strain Induced Crystallization ◽  
Induced Crystallization ◽  
Flow Induced Crystallization

ABSTRACT Strain-induced crystallization (SIC) and stress–strain relations of varied crosslink structures and varied crosslink densities of vulcanized natural rubber (NR), vulcanized synthetic polyisoprene rubber (IR), and un-vulcanized natural rubber are compared using a synchrotron X-ray. The onset strain of SIC does not depend on crosslink density and crosslink structures. Un-vulcanized NR shows a smaller onset strain of SIC than that of vulcanized NR. Therefore, entanglements in NR are pivot points to induce SIC, just as entanglements in semi-crystalline plastics induce flow-induced crystallization (FIC). During deformation, complicated phenomena occur simultaneously such as cavitation, crosslink breakdown, SIC with temperature upturn, and limited extensibility of chains between crosslinks, because rubber is a significantly inhomogeneous material. It is still difficult to evaluate the contribution of SIC to stress-upturn of the stress–strain relation of rubber.

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