Looking at Rubber Adhesion

1979 ◽  
Vol 52 (1) ◽  
pp. 23-42 ◽  
Author(s):  
A. D. Roberts

Abstract Rubber has been employed in contact with a variety of surfaces for decades, yet the adhesional mechanisms involved are not fully understood. This article describes fundamental investigations carried out over the last decade. Emphasis is placed upon the use of optical techniques for looking directly at the contact area rubber makes with another surface. The interpretation is based upon a rate-dependent surface energy approach. In this way it is possible to predict the level of peel adhesion between surfaces, for example, when a ball rolls on smooth rubber. Other examples treated in the same way are the time for detachment of a ball from a smooth rubber track under gravity, its resilience when bounced on the track, and its friction when slid over the track. The influence of surface roughness, electrostatic forces, surface bloom, and humidity are considered, together with rubber compound variables such as glass transition temperature, crosslink density, and fillers. The central theme is that the adhesional mechanisms all physically depend upon the product of surface properties and bulk viscoelasticity of the solids in contact.

2010 ◽  
Vol 25 (6) ◽  
pp. 1015-1019 ◽  
Author(s):  
Caijun Su ◽  
James A. LaManna ◽  
Yanfei Gao ◽  
Warren C. Oliver ◽  
George M. Pharr

The deformation behavior of amorphous selenium near its glass transition temperature (31 °C) has been investigated by uniaxial compression and nanoindentation creep tests. Cylindrical specimens compressed at high temperatures and low strain rates deform stably into barrel-like shapes, while tests at low temperatures and high strain rates lead to fragmentation. These results agree well with stress exponent and kinetic activation parameters extracted from nanoindentation creep tests using a similarity analysis. The dependence of the deformation modes on temperature and strain rate can be understood as a consequence of material instability and strain localization in rate-dependent solids.


2004 ◽  
Vol 18 (1) ◽  
pp. 63-67 ◽  
Author(s):  
C. C. Puig ◽  
H. E. H. Meijer ◽  
M. A. J. Michels ◽  
L. H. G. J. Segeren ◽  
G. J. Vancso

2016 ◽  
Vol 7 (1) ◽  
pp. 36-43 ◽  
Author(s):  
Jin Won Yu ◽  
Jin Jung ◽  
Yong-Mun Choi ◽  
Jae Hun Choi ◽  
Jaesang Yu ◽  
...  

Epoxy nanocomposites are fabricated by using diamine-functionalized GO and exhibit high Tg, tensile strength, and crosslink density.


1997 ◽  
Vol 70 (4) ◽  
pp. 641-649 ◽  
Author(s):  
V. Yu Levin ◽  
S. H. Kim ◽  
A. I. Isayev

Abstract Sulfur-cured non-reinforced SBR with different amounts of poly-, di- and monosulfidic crosslinks is devulcanized by high power ultrasound irradiation in a continuous process under various processing conditions. Total crosslink density, the proportion of polysulfidic crosslinks, gel fraction, and glass transition temperature are measured. The effect of the initial fraction of polysulfidic bonds on the devulcanization process is discussed.


1999 ◽  
Vol 72 (5) ◽  
pp. 854-861 ◽  
Author(s):  
Eduardo A. Gonzalez-de los Santos ◽  
Florentino Soriano-Corral ◽  
Ma Josefina Lozano-Gonzalez ◽  
Rodrigo Cedillo-Garcia

Abstract The present study describes the effect of ultrasonic irradiation on vulcanized guayule rubber using 1 to 3.5 parts per hundred of rubber (phr) of sulfur as the crosslink agent. The effect on crosslink density, gel fraction, torque and glass transition temperature was measured. After exposure to different powers of ultrasonic irradiation, the devulcanization effect was evident on the guayule rubber samples.


2002 ◽  
Vol 35 (5) ◽  
pp. 1491-1492 ◽  
Author(s):  
Fengchao Xie ◽  
H. F. Zhang ◽  
Fuk Kay Lee ◽  
Binyang Du ◽  
Ophelia K. C. Tsui ◽  
...  

Polymer ◽  
2004 ◽  
Vol 45 (6) ◽  
pp. 1939-1950 ◽  
Author(s):  
Jir-Shyr Chen ◽  
Christopher K Ober ◽  
Mark D Poliks ◽  
Yuanming Zhang ◽  
Ulrich Wiesner ◽  
...  

Author(s):  
Shawn A. Chester ◽  
Vikas Srivastava ◽  
Lallit Anand

Amorphous thermoplastic polymers are important engineering materials; however, their nonlinear, strongly temperature- and rate-dependent elastic-viscoplastic behavior is still not very well understood, and is modeled by existing constitutive theories with varying degrees of success. There is no generally agreed upon theory to model the large-deformation, thermo-mechanically-coupled, elastic-viscoplastic response of these materials in a temperature range which spans their glass transition temperature. Such a theory is crucial for the development of a numerical capability for the simulation and design of important polymer processing operations, and also for predicting the relationship between processing methods and the subsequent mechanical properties of polymeric products. In this manuscript we briefly summarize a few results from our own recent research [1–4] which is intended to fill this need.


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