scholarly journals Morphology Evolution, Molecular Simulation, Electrical Properties, and Rheology of Carbon Nanotube/Polypropylene/Polystyrene Blend Nanocomposites: Effect of Molecular Interaction between Styrene-Butadiene Block Copolymer and Carbon Nanotube

Polymers ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 230
Author(s):  
Ivonne Otero Otero Navas ◽  
Milad Kamkar ◽  
Mohammad Arjmand ◽  
Uttandaraman Sundararaj
Keyword(s):  
Carbon Nanotube ◽  
Block Copolymers ◽  
Molecular Simulation ◽  
Diblock Copolymers ◽  
Viscoelastic Behavior ◽  
Solubility Parameters ◽  
Integrated Network ◽  
Styrene Butadiene ◽  
The Impact ◽  
Blend Nanocomposites

This work studied the impact of three types of styrene-butadiene (SB and SBS) block copolymers on the morphology, electrical, and rheological properties of immiscible blends of polypropylene:polystyrene (PP:PS)/multi-walled carbon nanotubes (MWCNT) with a fixed blend ratio of 70:30 vol.%. The addition of block copolymers to PP:PS/MWCNT blend nanocomposites produced a decrease in the droplet size. MWCNTs, known to induce co-continuity in PP:PS blends, did not interfere with the copolymer migration to the interface and, thus, there was morphology refinement upon addition of the copolymers. Interestingly, the addition of the block copolymers decreased the electrical resistivity of the PP:PS/1.0 vol.% MWCNT system by 5 orders of magnitude (i.e., increase in electrical conductivity). This improvement was attributed to PS Droplets-PP-Copolymer-Micelle assemblies, which accumulated MWCNTs, and formed an integrated network for electrical conduction. Molecular simulation and solubility parameters were used to predict the MWCNT localization in the immiscible blend. The simulation results showed that diblock copolymers favorably interact with the nanotubes in comparison to the triblock copolymer, PP, and PS. However, the interaction between the copolymers and PP or PS is stronger than the interaction of the copolymers and MWCNTs. Hence, the addition of copolymer also changed the localization of MWCNT from PS to PS–PP–Micelles–Interface, as observed by TEM images. In addition, in the last step of this work, we investigated the effect of the addition of copolymers on inter- and intra-cycle viscoelastic behavior of the MWCNT incorporated polymer blends. It was found that addition of the copolymers not only affects the linear viscoelasticity (e.g., increase in the value of the storage modulus) but also dramatically impacts the nonlinear viscoelastic behavior under large deformations (e.g., higher distortion of Lissajous–Bowditch plots).

Viscoelastic Behavior of Styrene-Butadiene-Styrene Block Copolymers in Temperature Range of Glass-Rubber Transition of Styrene Block

1996 ◽  
Vol 69 (1) ◽  
pp. 73-80 ◽  
Author(s):  
N. Nakajima
Keyword(s):  
Molecular Weight ◽  
Block Copolymers ◽  
Viscoelastic Behavior ◽  
Shear Mode ◽  
Molecular Weight Polymer ◽  
Styrene Butadiene Styrene ◽  
The Difference ◽  
Tan Δ ◽  
Styrene Butadiene ◽  
Butadiene Styrene

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.

Free surface morphology of block copolymers: 1. Styrene-butadiene diblock copolymers

Polymer ◽  
1995 ◽  
Vol 36 (21) ◽  
pp. 3987-3996 ◽  
Author(s):  
Antonio Turturro ◽  
Ercole Gattiglia ◽  
Paolo Vacca ◽  
Gian Tommaso Viola
Keyword(s):  
Free Surface ◽  
Block Copolymers ◽  
Surface Morphology ◽  
Diblock Copolymers ◽  
Styrene Butadiene

Mechanical and Structural Consequences of Associative Dynamic Cross-Linking in Acrylic Diblock Copolymers

2019 ◽  
Author(s):  
Jacob Ishibashi ◽  
Yan Fang ◽  
Julia Kalow
Keyword(s):  
Block Copolymers ◽  
Rheological Properties ◽  
Diblock Copolymers ◽  
Cross Linking ◽  
Statistical Copolymer

<p>Block copolymers are used to construct covalent adaptable networks that employ associative exchange chemistry (vitrimers). The resulting vitrimers display markedly different nanostructural, thermal and rheological properties relative to those of their statistical copolymer-derived counterparts. This study demonstrates that prepolymer sequence is a versatile strategy to modify the properties of vitrimers.</p>

scholarly journals Analysis of the Impact on the Mechanical Properties of Modification of Oligohydroxyethers in Organic Solvent Solution with Rubbers

Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 519
Author(s):  
Vitalii Bezgin ◽  
Agata Dudek ◽  
Adam Gnatowski
Keyword(s):  
Mechanical Properties ◽  
Scientific Paper ◽  
Styrene Butadiene Rubber ◽  
Butadiene Rubber ◽  
Molecular Weights ◽  
Wide Range ◽  
Strength Tests ◽  
Materials Used ◽  
Styrene Butadiene ◽  
The Impact

This paper proposes and presents the chemical modification of linear hydroxyethers (LHE) with different molecular weights (380, 640, and 1830 g/mol) with the addition of three types of rubbers (polysulfide rubber (PSR), polychloroprene rubber (PCR), and styrene-butadiene rubber (SBR)). The main purpose of choosing this type of modification and the materials used was the possibility to use it in industrial settings. The modification process was conducted for a very wide range of modifier additions (rubber) per 100 g LHE. The materials obtained in the study were subjected to strength tests in order to determine the effect of the modification on functional properties. Mechanical properties of the modified materials were improved after the application of the modifier (rubber) to polyhydroxyether (up to certain modifier content). The most favorable changes in the tested materials were registered in the modification of LHE-1830 with PSR. In the case of LHE-380 and LHE-640 modified in cyclohexanol (CH) and chloroform (CF) solutions, an increase in the values of the tested properties was also obtained, but to a lesser extent than for LHE-1830. The largest changes were registered for LHE-1830 with PSR in CH solution: from 12.1 to 15.3 MPa for compressive strength tests, from 0.8 to 1.5 MPa for tensile testing, from 0.8 to 14.7 MPa for shear strength, and from 1% to 6.5% for the maximum elongation. The analysis of the available literature showed that the modification proposed by the authors has not yet been presented in any previous scientific paper.

Toughening of Polypropylene-Ethylene Copolymer with Nanosized CaCO3 and Styrene-Butadiene-Styrene

2007 ◽  
Vol 121-123 ◽  
pp. 1451-1454
Author(s):  
Jian Feng Chen ◽  
Guo Quan Wang ◽  
Xiao Fei Zeng ◽  
Hong Ying Zhao
Keyword(s):  
Average Particle Size ◽  
Average Particle ◽  
Single Screw Extruder ◽  
Roll Mill ◽  
The Matrix ◽  
Ethylene Copolymer ◽  
Styrene Butadiene Styrene ◽  
Styrene Butadiene ◽  
The Impact ◽  
Butadiene Styrene

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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