scholarly journals Strain-Induced Form Transition and Crystallization Behavior of the Transparent Polyamide

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1028
Author(s):  
Chenxu Zhou ◽  
Siyuan Dong ◽  
Ping Zhu ◽  
Jiguang Liu ◽  
Dujin Wang ◽  
...  

A transparent polyamide, poly(4,4′-aminocyclohexyl methylene dodecanedicarboxylamide) (PAPACM12), was studied and characterized by in situ wide-angle X-ray diffraction (WAXD) to establish the relationship between its crystallization behavior, crystalline form transition under external fields, and macroscopic properties. During the heating process, cold crystallization occurred and increased, and there was no form transition below the melting point. During the isothermal process, PAPACM12 exhibited the same crystalline structure as that during the heating process. The crystalline structure of PAPACM12 was attributed to α-form crystal, which is the stable form, according to the WAXD diffraction peaks of the conventional AABB-type polyamides. During stretching deformation, the crystal transition from α-form to γ-form and strain-induced crystallization were observed to contribute to the PAPACM12 with higher breaking strength and elongation. This study firstly determine the crystalline structure of transparent polyamides, and then the controlled strain-induced crystallization and transformation are demonstrated to be effective preparation methods for polyamides with high properties.

RSC Advances ◽  
2015 ◽  
Vol 5 (32) ◽  
pp. 25171-25182 ◽  
Author(s):  
Xuan Fu ◽  
Guangsu Huang ◽  
Zhengtian Xie ◽  
Wang Xing

The existence of a denser network domain formed by incorporation of filler and its vital role in determining the strain-induced crystallization behavior of nanocomposites is proved by in situ synchrotron X-ray diffraction characterization.


2021 ◽  
Vol 17 (3) ◽  
pp. 217-225
Author(s):  
Abdulhakim Masa ◽  
Nabil Hayeemasae ◽  
Siriwat Soontaranon ◽  
Mohd Hanif Mohd Pisal ◽  
Mohamad Syahmie Mohamad Rasidi

The performance of natural rubber (NR) relies heavily on the microstructural changes during deformation. This has brought to significant change in the stress response of NR. Besides, the stretching rate may also affect the stress response of NR. In this study, effects of stretching rate on tensile deformation and strain-induced crystallization of crosslinked NR were investigated. Results indicated that increasing the strain rate has increased the stress at given strain where the onset of strain-induced crystallization was shifted to a lower strain. The crystallinity of the crosslinked NR was shown to be higher at a high stretching rate and it corresponded well with the tensile response. The results clearly confirm that chain orientation and crystallization became stronger with increasing deformation rate. The study also suggests that the deformation could improve distribution of crosslinked network structures.


Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2507
Author(s):  
Jinxian Zhai ◽  
Hanpeng Zhao ◽  
Xiaoyan Guo ◽  
Xiaodong Li ◽  
Tinglu Song

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.


Soft Matter ◽  
2019 ◽  
Vol 15 (4) ◽  
pp. 734-743 ◽  
Author(s):  
Pinzhang Chen ◽  
Jingyun Zhao ◽  
Yuanfei Lin ◽  
Jiarui Chang ◽  
Lingpu Meng ◽  
...  

The structural evolution of NR during stretching at −40 °C and in the strain–temperature space.


Crystals ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 294 ◽  
Author(s):  
Konrad Schneider ◽  
Matthias Schwartzkopf

Vulcanized natural rubber (unfilled and filled with 20 phr carbon black) is strained. We suppress the macroscopic formation of fiber symmetry by choosing strip-shaped samples ("pure-shear geometry") and investigate the orientation of the resulting crystallites by two-dimensional wide-angle X-ray diffraction (WAXD), additionally rotating the sample tape about the straining direction. Indications of a directed reinforcing effect of the strain-induced crystallization (SIC) in the thin strip are found. In the filled material fewer crystallites are oriented and the orientation distribution of the oriented crystallites is less perfect. The results confirm, that it is important for the evaluation of crystallinity under deformation to check, whether fiber symmetry can be assumed. This has consequences in particular on the quantitative interpretation of space-resolved scanning experiments in the vicinity of crack tips. Furthermore it raises the question, whether there is an asymmetric reinforcing effect of the SIC in the vicinity of crack tips inside natural rubber.


2015 ◽  
Vol 132 (39) ◽  
pp. n/a-n/a ◽  
Author(s):  
Abdulhakim Masa ◽  
Sougo Iimori ◽  
Ryota Saito ◽  
Hiromu Saito ◽  
Tadamoto Sakai ◽  
...  

2005 ◽  
Vol 38 (16) ◽  
pp. 7064-7073 ◽  
Author(s):  
Shigeyuki Toki ◽  
Igors Sics ◽  
Benjamin S. Hsiao ◽  
Masatoshi Tosaka ◽  
Sirilux Poompradub ◽  
...  

Author(s):  
Peiling Liu ◽  
Benshan Zhang ◽  
Qun Shen ◽  
Xiaosong Hu ◽  
Wenhao Li

Noncrystalline granular (NCG) starch is a peculiar form of starch. The granules have granular shape but no crystalline structure. It is a middle state between native semi-crystal structure and paste. The conception of NCG starch was presented and its preparation methods for native maize starch were explored. Cross-linking by chloroepoxy propane was adopted as the chemical method while ethanol treatment was adopted as the physical method. Cross bonds and ethanol were both able to protect starch granules from swelling while thermal treatment was able to destroy crystalline structure of the granules. The structure of granule was observed by polarization microscope and scanning electron microscopy (SEM). Change from crystalline to noncrystalline structure was confirmed by X-ray diffraction (XRD). It indicated that preparation of NCG starch with the physical method was better than chemical method. The detailed conditions were: maize starch (40%, w/w) was slurried in 50%-ethanol, underwent thermal treatment at 85°C for 2 minutes, washed with anhydrous ethanol (2000 ml), and freeze dried.


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