Study on the relationship between the mechanical properties and processing for self-reinforced polymers. Part 1: A theory of stress-induced crystallization for entangled polymer networks

1993 ◽  
Vol 271 (10) ◽  
pp. 911-929 ◽  
Author(s):  
M. S. Song ◽  
G. X. Hu ◽  
Q. R. Zhu
Keyword(s):  
Mechanical Properties ◽  
Polymer Networks ◽  
Reinforced Polymers ◽  
Entangled Polymer ◽  
The Relationship ◽  
Stress Induced Crystallization ◽  
Induced Crystallization

scholarly journals Influence of Temperature on Mechanical Properties of P(BAMO-r-THF) Elastomer

Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2507
Author(s):  
Jinxian Zhai ◽  
Hanpeng Zhao ◽  
Xiaoyan Guo ◽  
Xiaodong Li ◽  
Tinglu Song
Keyword(s):  
Mechanical Properties ◽  
X Ray Diffraction ◽  
Polymeric Chains ◽  
Different Temperatures ◽  
Influence Of Temperature On ◽  
Strain Induced Crystallization ◽  
Thermal Histories ◽  
Static Conditions ◽  
The Relationship ◽  
Induced Crystallization

The relationship between temperature and the mechanical properties of an end cross-linked equal molar random copolyether elastomer of 3,3-bis(azidomethyl)oxetane and tetrahydrofuran (P(BAMO-r-THF)) was investigated. During this investigation, the performances of two P(BAMO-r-THF) elastomers with different thermal histories were compared at different temperatures. The elastomer as prepared at 20 °C (denoted as S0) exhibited semi-crystallization morphology. Wide angle X-ray diffraction analysis indicated that the crystal grains within elastomer S0 result from the crystallization of BAMO micro-blocks embedded in P(BAMO-r-THF) polymeric chains, and the crystallinity is temperature irreversible under static conditions. After undergoing a heating-cooling cycle, this elastomer became an amorphous elastomer (denoted as S1). Regarding mechanical properties, at 20 °C, break strains and stresses of 315 ± 22% and 0.46 ± 0.01 MPa were obtained for elastomer S0; corresponding values of 294 ± 6% and 0.32 ± 0.02 MPa were obtained for elastomer S1. At −40 °C, these strains and stresses simultaneously increased to 1085 ± 21% and 8.90 ± 0.72 MPa (S0) and 1181 ± 25% and 10.23 ± 0.44 MPa (S1), respectively, owing to the strain-induced crystallization of BAMO micro-blocks within the P(BAMO-r-THF) polymeric chains.

scholarly journals Mechanical properties of end-crosslinked entangled polymer networks using sliplink Brownian dynamics simulations

2006 ◽  
Vol 46 (1) ◽  
pp. 95-109 ◽  
Author(s):  
Julian Oberdisse ◽  
Giovanni Ianniruberto ◽  
Francesco Greco ◽  
Giuseppe Marrucci
Keyword(s):  
Mechanical Properties ◽  
Brownian Dynamics ◽  
Polymer Networks ◽  
Entangled Polymer ◽  
Dynamics Simulations ◽  
Brownian Dynamics Simulations

Sunlight exposure: the effects on the performance of paragliding fabric

2018 ◽  
Vol 69 (05) ◽  
pp. 381-389
Author(s):  
MENGÜÇ GAMZE SÜPÜREN ◽  
TEMEL EMRAH ◽  
BOZDOĞAN FARUK
Keyword(s):  
Mechanical Properties ◽  
Aging Process ◽  
Air Permeability ◽  
Sunlight Exposure ◽  
Test Results ◽  
Coating Materials ◽  
Strength Tests ◽  
Before And After ◽  
The Relationship ◽  
Dark Blue

This study was designed to explore the relationship between sunlight exposure and the mechanical properties of paragliding fabrics which have different colors, densities, yarn counts, and coating materials. This study exposed 5 different colors of paragliding fabrics (red, turquoise, dark blue, orange, and white) to intense sunlight for 150 hours during the summer from 9:00 a.m. to 3:00 p.m. for 5 days a week for 5 weeks. Before and after the UV radiation aging process, the air permeability, tensile strength, tear strength, and bursting strength tests were performed. Test results were also evaluated using statistical methods. According to the results, the fading of the turquoise fabric was found to be the highest among the studied fabrics. It was determined that there is a significant decrease in the mechanical properties of the fabrics after sunlight exposure. After aging, the fabrics become considerably weaker in the case of mechanical properties due to the degradation in both the dyestuff and macromolecular structure of the fiber

scholarly journals Water lubrication of graphene oxide-based materials

Friction ◽  
2021 ◽  
Author(s):  
Shaoqing Xue ◽  
Hanglin Li ◽  
Yumei Guo ◽  
Baohua Zhang ◽  
Jiusheng Li ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Graphene Oxide ◽  
Lubrication Theory ◽  
Lubricant Additives ◽  
Water Lubrication ◽  
Broad Application ◽  
Water Dispersibility ◽  
Metal Processing ◽  
The Relationship ◽  
Ph Concentration

AbstractWater is as an economic, eco-friendly, and efficient lubricant that has gained widespread attention for manufacturing. Using graphene oxide (GO)-based materials can improve the lubricant efficacy of water lubrication due to their outstanding mechanical properties, water dispersibility, and broad application scenarios. In this review, we offer a brief introduction about the background of water lubrication and GO. Subsequently, the synthesis, structure, and lubrication theory of GO are analyzed. Particular attention is focused on the relationship between pH, concentration, and lubrication efficacy when discussing the tribology behaviors of pristine GO. By compounding or reacting GO with various modifiers, amounts of GO-composites are synthesized and applied as lubricant additives or into frictional pairs for different usage scenarios. These various strategies of GO-composite generate interesting effects on the tribology behaviors. Several application cases of GO-based materials are described in water lubrication, including metal processing and bio-lubrication. The advantages and drawbacks of GO-composites are then discussed. The development of GO-based materials for water lubrication is described including some challenges.

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