scholarly journals Structure and Dielectric Properties of Electroactive Tetraaniline Grafted Non-Polar Elastomers

2020 ◽  
Vol 4 (1) ◽  
pp. 25
Author(s):  
Christopher Ellingford ◽  
Atcharaporn Pengchaicharoen ◽  
Alan M. Wemyss ◽  
Chaoying Wan

Intrinsic modification of polybutadiene and block copolymer styrene–butadiene–styrene with the electrically conducting emeraldine salt of tetraaniline (TANI) via a three-step grafting method, is reported in this work. Whilst the TANI oligomer grafted at a similar rate to both polybutadiene and styrene–butadiene–styrene under the same conditions, the resulting elastomers exhibited vastly different properties. 1 mol% TANI-PB exhibited an increased relative permittivity of 5.9, and a high strain at break of 156%, whilst 25 mol% TANI-SBS demonstrated a relative permittivity of 6.2 and a strain at break of 186%. The difference in the behaviour of the two polymers was due to the compatibilisation of TANI by styrene in SBS through π-π stacking, which prevented the formation of a conducting TANI network in SBS at. Without the styrene group, TANI-PB formed a phase separated structure with high levels of TANI grafting. Overall, it was concluded that the polymer chain structure, the morphology of the modified elastomers, and the degree of grafting of TANI, had the greatest effect on the mechanical and dielectric properties of the resultant elastomers. This work paves the way for an alternative approach to the extrinsic incorporation of conducting groups into unsaturated elastomers, and demonstrates dielectric elastomers with enhanced electrical properties for use in actuation devices and energy harvesting applications.

1996 ◽  
Vol 69 (1) ◽  
pp. 73-80 ◽  
Author(s):  
N. Nakajima

Abstract Dynamic mechanical measurements were performed with styrene-butadiene-styrene (SBS) block copolymers, Kraton D-1101 and D-l 102. Isochronal data were obtained from −130 to 85°C in the tensile mode at 1 Hz and from 60 to 160°C in the shear mode at 1 rad/s. The isothermal measurements were also performed at 60, 90, 120, 140, and 160°C in the frequency range of 0.0316 to 100 rad/s. The results suggest that the two polymers have different morphologies although the styrene content and the diblock content are about the same for both polymers. Kraton D-1101, which has 1.5 times higher molecular weight, has 3–5 times higher rubbery modulus, compared to D-1102. The lower molecular weight polymer, D-1102, appears to have a larger amount of the mixed phase at the boundary. This is suggest by the lower temperature of the “domain disruption”, Tdd and the higher magnitude of tan δ at Tdd. This explains the difference in the rubbery moduli of the two polymers.


CrystEngComm ◽  
2020 ◽  
Vol 22 (7) ◽  
pp. 1261-1272 ◽  
Author(s):  
Daniela Caruntu ◽  
Benard Kavey ◽  
Suporna Paul ◽  
Alin Ciprian Bas ◽  
Aurelian Rotaru ◽  
...  

Polymer–ceramic nanocomposite films comprising ceramic nanoparticles dispersed in a polymer matrix (0–3 composites) have garnered increasing interest due to their superior performance characteristics, and can be used in flexible modern electronics and energy storage systems.


2017 ◽  
Vol 90 (3) ◽  
pp. 550-561 ◽  
Author(s):  
Prithwiraj Mandal ◽  
Siva Ponnupandian ◽  
Soumyadip Choudhury ◽  
Nikhil K. Singha

ABSTRACT Thiol-ene modification of high vinyl content thermoplastic elastomeric styrene butadiene styrene (SBS) block copolymer (BCP) was carried out using different thiolating agents in toluene at 70 °C. 1H NMR analysis confirmed the participation of vinyl double bond in the thiol-ene modification reaction of SBS. Surface morphology of the block copolymers evaluated by atomic force microscopy analysis showed higher roughness after the thiol-ene reaction. The thiol-modified SBS block copolymer showed better adhesion strength and oil resistance properties than the pristine SBS.


Polymers ◽  
2021 ◽  
Vol 13 (14) ◽  
pp. 2249
Author(s):  
Bei Chen ◽  
Fuqiang Dong ◽  
Xin Yu ◽  
Changjiang Zheng

In order to solve the problems caused by asphalt diseases and prolong the life cycle of asphalt pavement, many studies on the properties of modified asphalt have been conducted, especially polyurethane (PU) modified asphalt. This study is to replace part of the styrene-butadiene-styrene (SBS) modifier with waste polyurethane (WP), for preparing WP/SBS composite modified asphalt, as well as exploring its properties and microstructure. On this basis, this paper studied the basic performance of WP/SBS composite modified asphalt with a conventional performance test, to analyze the high- and low-temperature rheological properties, permanent deformation resistance and storage stability of WP/SBS composite modified asphalt by dynamic shear rheometer (DSR) and bending beam rheometer (BBR) tests. The microstructure of WP/SBS composite modified asphalt was also observed by fluorescence microscope (FM) and Fourier transform infrared spectroscopy (FTIR), as well as the reaction between WP and asphalt. According to the results of this study, WP can replace SBS as a modifier to prepare WP/SBS composite modified asphalt with good low-temperature resistance, whose high-temperature performance will be lower than that of SBS modified asphalt. After comprehensive consideration, 4% SBS content and 15% WPU content (4 S/15 W) are determined as the suitable types of WPU/SBS composite modified asphalt.


2021 ◽  
pp. 51000
Author(s):  
Fathin Hani Azizul Rahim ◽  
Abdul Aziz Saleh ◽  
Raa Khimi Shuib ◽  
Ku Marsilla Ku Ishak ◽  
Zuratul Ain Abdul Hamid ◽  
...  

2007 ◽  
Vol 121-123 ◽  
pp. 1451-1454
Author(s):  
Jian Feng Chen ◽  
Guo Quan Wang ◽  
Xiao Fei Zeng ◽  
Hong Ying Zhao

Nanocomposites of nanosized-CaCO3/polypropylene-ethylene copolymer (PPE) and nanosized CaCO3/ PPE/ styrene-butadiene-styrene (SBS) were prepared by using two-roll mill and single screw extruder. The average particle size of nanosized CaCO3 was determined to be about 30 nm. By adding nanosized CaCO3 into PPE matrix, the toughness of the matrix improves significantly. At nanosized CaCO3 content of 12 phr (parts per hundred PPE resin by weight), the impact strength of CaCO3/PPE at room temperature reaches 61.6 KJ/m2, which is 3.02 times that of unfilled PPE matrix. In addition, the synergistic toughening effect of nanosized CaCO3 and SBS particles on PPE matrix was investigated.


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