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Chinese Journal of Materials Research  2014, Vol. 28 Issue (10): 794-800    DOI: 10.11901/1005.3093.2014.221
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Preparation and Properties of Organoclay/Polyethersulfone/Epoxy Hybrid Nanocomposites
Shou MA1,2,**(),Jianchun GUO1
1. State Key Laboratory of Oil and Gas Geology and Exploitation, Southwest Petroleum University, Chengdu 637000
2. SINOPEC Shengli Oilfield Company, Dongying 257082
Cite this article: 

Shou MA,Jianchun GUO. Preparation and Properties of Organoclay/Polyethersulfone/Epoxy Hybrid Nanocomposites. Chinese Journal of Materials Research, 2014, 28(10): 794-800.

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Abstract  

Organoclay/polyethersulphone/epoxy hybrid nanocomposites were prepared by solvent method and melting method, respectively. Their tensile properties, fracture toughness, thermal properties and microstructures were then characterized. Their tensile strength arrived at 75 MPa, modulus reached 2.8GPa, and fracture toughness was over 1.1MPam1/2. Synergistic toughening effect of the polyethersulphone and organoclay on the epoxy resin was observed. Semi-interpenetrating network of the polyethersulphone/epoxy matrix was found by dynamic mechanical thermal analyzer (DMA) and transmission electron microscope (TEM). The results of X-ray diffractometer (XRD) analysis and TEM observation reveal that the organoclay possessed ordered exfoliated morphologies. Glass transition temperatures (Tgs) of the two hybrid nanocomposites were tested by dynamic mechanical thermal analysis (DMTA). The Tg of the specimen prepared by the solvent method was found higher than 170℃, while that by the melting method was more than 180℃.

Key words:  composites      hybrid nanocomposite      polyethersulphone      organoclay      fracture toughness      microstructure     
Received:  28 April 2014     
Fund: * Supported by National Science and Technology Major Project No.2011ZX05051.

URL: 

https://www.cjmr.org/EN/10.11901/1005.3093.2014.221     OR     https://www.cjmr.org/EN/Y2014/V28/I10/794

Fig.1  DMTA curves of Loss tangent vs. temperature for the samples consisting of the neat epoxy resin, PES/epoxy blend, nanocomposites and hybrid nanocomposites
Fig.2  SEM images for the fractured cross-sections of the samples after being rinsed (from (a-1) to (a-6)) and before being rinsed (from (b-1) to (b-6))(All the samples were sufficiently rinsed with methylene chloride) ((a-1), (b-1): organoclay(0%)/PES/epoxy samples cured at 120℃; (a-2), (b-2): organoclay(1%)/PES/epoxy samples cured at 120℃; (a-3), (b-3): organoclay(3%)/PES/epoxy samples cured at 120℃; (a-4), (b-4): organoclay(0%)/PES/epoxy samples cured at 180℃; (a-5), (b-5): organoclay(1%)/PES/epoxy samples cured at 180℃; (a-6), (b-6): organoclay(3%)/PES/epoxy samples cured at 180℃)
0% organoclay 1% organoclay 3% organoclay
Group 1 192℃ 189℃ 181℃
Group 2 181℃ 177℃ 175℃
Group 3 185℃ 182℃ 174℃
Group 4 194℃ 192℃ 187℃
Table 1  Tgs of the four groups of samples
Fig.3  TEM micrographs of PES/epoxy blends and neat epoxy resin with homogeneous morphology (A) PES/epoxy blends (cured at 120℃); (B) PES/epoxy blends(cured at 180℃); (C) neat epoxy resin (cured at 120℃)
Fig.4  XRD patterns of prinstine clay, organoclay, nanocomposites and hybrid nanocomposites (A) organoclay(1%)/PES/epoxy sample cured at 120℃; (B) organoclay(3%)/PES/epoxy sample cured at 120℃; (C) organoclay(1%)/PES/epoxy sample cured at 180℃; (D) organoclay(3%)/PES/epoxy sample cured at 180℃; (E) organoclay(1%)/epoxy sample; (F) organoclay(3%)/epoxy sample; (G) pristine clay; (H) organoclay
Fig.5  TEM images of the morphologies of organoclay in the hybrid nanocomposites with 1% organoclay(a), small agglomerates of organoclay(b) and large agglomerates of organoclay) (c, d)
Sample 2θ (°) Intensity D-spacing(nm)
Organoclay (1%)/PES/epoxy 1.062 1024 9.23
Organoclay (3%)/PES/epoxy 1.068 1065 9.18
Table 2  XRD data of the hybrid nanocomposites prepared by melting method
Fig.6  TEM images of the morphologies of organoclay in the hybrid nanocomposites with 1% organoclay
Sample Tensile strength (MPa) Tensile modulus (GPa) Elongation (%)
Epoxy resin 75.63±1.95 2.92±0.19 2.58±0.36
PES/epoxy by solvent method 78.36±2.31 2.88±0.06 2.94±0.24
Organoclay(1%)/PES/epoxy by solvent method 76.03±2.11 3.03±0.07 2.78±0.29
Organoclay(3%)/PES/epoxy by solvent method 72.49±1.89 3.11±0.08 2.71±0.42
Organoclay(1%)/PES/epoxy by melting method 77.19±3.06 2.98±0.13 2.74±0.62
Organoclay(3%)/PES/epoxy by melting method 73.08±2.02 3.01±0.12 2.61±0.51
Table 3  Tensile testing results of the epoxy resin, PES/epoxy blend and hybrid nanocomposites
Solvent method
(cured at 120℃) neat epoxy organoclay(1%)/epoxy organoclay(1%)/epoxy
KIC (MPa m1/2) 0.58±0.11 0.73±0.05 0.81±0.06
(cured at 180℃) PES/epoxy organoclay(1%)/PES/epoxy organoclay(3%)/PES/epoxy
KIC (MPa m1/2) 0.73±0.03 0.78±0.02 0.80±0.02
(cured at 120℃) PES/epoxy organoclay(1%)/PES/epoxy organoclay(3%)/PES/epoxy
KIC (MPa m1/2) 0.77±0.10 1.15±0.10 0.93±0.05
Melting method
(cured at 120℃) PES/epoxy organoclay(1%)/PES/epoxy organoclay(3%)/PES/epoxy
KIC (MPa m1/2) 0.78±0.13 1.12±0.14 1.02±0.10
Table 4  Fracture toughness of the neat epoxy resins, PES/epoxy blends, nanocomposites and hybrid nanocomposites cured at different temperatutes (KIC stands for the critical value of Mode-I fracture toughness)
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