Structure-Property Relationship of a Thermoplastic Vulcanizate (Tpv)/Layered Silicate Nanocomposites Prepared Using Maleic Anhydride Modified Polypropylene as a Compatibilizer

2005 ◽  
Vol 78 (1) ◽  
pp. 42-53 ◽  
Author(s):  
Joy K. Mishra ◽  
Il Kim ◽  
Chang-Sik Ha ◽  
Jin-Ho Ryou ◽  
Gue-Hyun Kim

Abstract Thermoplastic vulcanizate(TPV)/organoclay nanocomposites have been successfully prepared by melt intercalation method. Maleic anhydride modified polypropylene has been used as a compatibilizer. The TPV/organoclay nanocomposites have been characterized by Fourier-transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) and Transmission Electron Microscope (TEM). The nanocomposite as evidenced by X-ray diffraction is an intercalated one. The nanocomposites exhibited remarkable improvement in tensile and storage modulus over their pristine counterpart. The dynamic mechanical analysis reveals that the glass transition temperature of the polypropylene phase of the nanocomposite is increased (compared to its pristine counterpart), whereas the EPDM phase remains same. The nanocomposites showed improved solvent resistance over its pristine counterpart. The structure-property correlation of the nanocomposites is attempted.

2006 ◽  
Vol 951 ◽  
Author(s):  
Hsiu-Yu Cheng ◽  
Guang-Way William Jang

ABSTRACTPolymer/SWN nanocomposites were synthesized in the soap-free emulsion polymerization of methyl methacrylate (MMA) using 2-hydroxylethyl methacrylate (HEMA). The SWN in the polymer/SWN nanocomposites was individually dispersed in water, and these are adsorbed on the surface of monomer droplets. Polymer/SWN nanocomposites were obtained by adding an aqueous dispersion of layered silicate to the polymer emulsion. X-ray diffraction (XRD) and FT-IR spectra were utilized to characterize the structures of the nanocomposites. The degree of dispersion of these nanocomposites was investigated by transmission electron microscopy (TEM). Furthermore, the thermal and mechanical properties of polymer/SWN nanocomposites were determined using thermogravimetric analysis (TGA), differential scanning calorimeter (DSC) and dynamic mechanical analysis (DMA). The increased tanδ of the obtained nanocomposites is caused by the fine dispersion of SWN particles into the polymer matri


2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Guiyun Yi ◽  
Baolin Xing ◽  
Jianbo Jia ◽  
Liwei Zhao ◽  
Yuanfeng Wu ◽  
...  

Macroporous TiO2photocatalyst was synthesized by a facile nanocasting method using polystyrene (PS) spherical particles as the hard template. The synthesized photocatalyst was characterized by transmission electron microscope (TEM), scanning electron microscopy (SEM), thermogravimetry-differential thermogravimetry (TG-DTG), X-ray diffraction (XRD), and N2-sorption. TEM, SEM, and XRD characterizations confirmed that the macroporous TiO2photocatalyst is composed of anatase phase. The high specific surface area of 87.85 m2/g can be achieved according to the N2-sorption analysis. Rhodamine B (RhB) was chosen as probe molecule to evaluate the photocatalytic activity of the TiO2catalysts. Compared with the TiO2materials synthesized in the absence of PS spherical template, the macroporous TiO2photocatalyst sintered at 500°C exhibits much higher activity on the degradation of RhB under the UV irradiation, which can be assigned to the well-structured macroporosity. The macroporous TiO2material presents great potential in the fields of environmental remediation and energy conversion and storage.


NANO ◽  
2016 ◽  
Vol 11 (12) ◽  
pp. 1650132 ◽  
Author(s):  
Jie Yang ◽  
Dawei Li ◽  
Zengyuan Pang ◽  
Qufu Wei

A novel nanomaterial composed of copper and carbon nanofibers (CuCNFs) decorated with Ag-doped TiO2 (Ag–TiO[Formula: see text] nanoparticles was prepared through electrospinning, carbonization and solvothermal treatment. The composites were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and electrochemical impedance spectroscopy (EIS). The obtained composites were mixed with laccase and Nafion to construct novel hydroquinone biosensor. The electrochemical behavior of the novel biosensor was studied using cyclic voltammetry (CV) and chronoamperometry. The results demonstrated that the biosensor possessed a wide detection linear range (1.20–176.50[Formula: see text][Formula: see text]M), a good selectivity, repeatability, reproducibility and storage stability. This work provides a new material to design more efficient laccase (Lac) based biosensor for hydroquinone detection.


2008 ◽  
Vol 8 (4) ◽  
pp. 1858-1866 ◽  
Author(s):  
Pralay Maiti ◽  
Jaya P. Prakash Yadav

Copolymer of hydroxybutyrate and hydroxyvalerate, P(HB-HV)/layered silicate or hydroxyapatite nanocomposites were prepared via melt extrusion. The nanostructure, as observed from wide-angle X-ray diffraction and transmission electron microscopy, indicate intercalated hybrids for layered silicates. Hydroxyapatite of nanometer dimension is uniformly distributed in matrix copolymer. The nanohybrids show significant improvement in thermal and mechanical properties of the copolymer as compared to the neat copolymer. The layered silicate nanocomposites exhibit superior mechanical properties as compared to hydroxyapatite nanohybrid. The thermal expansion coefficient is significantly reduced in nanohybrids. The biodegradability of pure copolymer and its nanocomposites were studied at room temperatures under controlled conditions in compost media. The rate of biodegradation of copolymer is enhanced dramatically in the nanohybrids. Hydroxyapatite hybrid shows highest rate of biodegradation. The change in biodegradation is streamlined in terms of nature of nanoparticles used to prepare hybrids.


2010 ◽  
Vol 123-125 ◽  
pp. 247-250
Author(s):  
Yu Qing Zhang ◽  
Yu Xin He ◽  
Li Zhang ◽  
Jun Xian Li

A new type of EVA-g-PU/OMMT nanocomposites was synthesized through the method of chemical modification and melt intercalation. FTIR testing showed that the PU prepolymer was grafted on EVA main chains successfully. The structures of EVA-g-PU/OMMT nanocomposites were characterized by X-ray diffraction (XRD) and by high-resolution transmission electron microscopy (HRTEM). The enhanced storage modulus of EVA-g-PU/OMMT nanocomposites was characterized by dynamic mechanical analysis (DMA). The thermal stabilities of EVA/clay nanocomposites were also studied by thermal gravimetric analysis (TGA). Mechanical testing showed that the tensile strength and tear strength of EVA-g-PU/OMMT nanocomposites were far superior to pure EVA.


2004 ◽  
Vol 03 (04n05) ◽  
pp. 663-669 ◽  
Author(s):  
S.-J. PARK ◽  
F.-L. JIN ◽  
J.-R. LEE

A novel nanocomposites of modified clay in a glassy epoxy were prepared using a direct melt intercalation technique. The contents of oganoclay were varied with 0, 1, 2, and 3 wt% and N-benzylpyrazinium hexafluoroantimonate (BPH) was used for curing of epoxy matrix as a cationic latent catalyst. Dynamic mechanical analysis (DMA) measurement was performed to examine the glass transition temperature of the nanocomposites. As a result, X-ray diffraction indicated the intercalation of the epoxy chains happening inside the gallery of clay. The nanocomposites showed a higher glass transition temperature and storage modulus than those of the pristine epoxy. The mechanical interfacial properties of the nanocomposites were also investigated and the improvement in tearing energy of 160% over pristine epoxy was obtained.


1994 ◽  
Vol 341 ◽  
Author(s):  
D. Prasad Beesabathina ◽  
L. Salmanca-Riba ◽  
M. S. Hegde ◽  
K. M. Satyalakshmi ◽  
K. V. R. Prasad ◽  
...  

AbstractThin films of Bi2VO5.5 (BVO), a vanadium analog of the n = I member of the Aurivillius family, have been prepared by pulsed laser deposition. The BVO films grow along the [001] direction on LaNiO3(LNO) and YBa2Cu3O7 (YBCO) electrode buffer layers on LaA- IO3(LAO) substrates as obtained from X-ray diffraction studies. The microstructure of the films and of the interfaces within the film and between the film and the substrate were characterized using transmission electron microscopy. The in-plane epitaxial relationship of the rhombohedral LNO on perovskite LAO was [100] LNO // [100] LAO and [001] LNO // [001] LAO. High resolution lattice images showed a sharp interface between LNO and LAO. However, the LNO film is twinned with a preferred orientation along the growth direction. The BVO layer is single crystalline on both LNO/LAO and YBCO/LAO with the caxis parallel to the growth direction except for a thin layer of about 400 Å at the interface which is polycrystalline.


e-Polymers ◽  
2008 ◽  
Vol 8 (1) ◽  
Author(s):  
Cuneyt Bagcioglu ◽  
Sinan Sen ◽  
Yusuf Yagci ◽  
Turgut Nugay ◽  
Nihan Nugay

AbstractHighly toughened super high-impact polystyrene (HIPS)/organophilic montmorillonite (Org-MMT) nanocomposite was prepared by solution blending method. Organophilic modification of MMT layered silicate was achieved by using a special toughener-intercalant, quaternary ammonium salt of α-tertiary amine functionalized polybutadiene and shown by X-ray diffraction analysis. The resulting HIPS/Org-MMT nanocomposite was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), atomic force microscopy (AFM), thermogravimetric analysis (TGA), and static and dynamic mechanical analyses. The morphological study of HIPS/Org-MMT nanocomposite showed that nanolayers were exfoliated in nanocomposite and moreover caused much more well dispersed and reduced PS occluded rubber domains. This mechanism was found to be responsible for dramatic increase in toughness of nanocomposites. Additionally, improved thermal and dynamic mechanical properties of the resultant nanocomposite promises to open a new way for highly toughened super HIPSs via nanocomposite assemblies even with a very low degree of clay loading.


2016 ◽  
Vol 2016 ◽  
pp. 1-13 ◽  
Author(s):  
Alice Tesarikova ◽  
Dagmar Merinska ◽  
Jiri Kalous ◽  
Petr Svoboda

Two ethylene-octene copolymers with 17 and 45 wt.% of octene (EOC-17 and EOC-45) were compared in nanocomposites with Cloisite 93A. EOC-45 nanocomposites have a higher elongation at break. Dynamical mechanical analysis (DMA) showed a decrease oftan⁡δwith frequency for EOC-17 nanocomposites, but decrease is followed by an increase for EOC-45 nanocomposites; DMA showed also increased modulus for all nanocomposites compared to pure copolymers over a wide temperature range. Barrier properties were improved about 100% by addition of organoclay; they were better for EOC-17 nanocomposites due to higher crystallinity. X-ray diffraction (XRD) together with transmission electron microscopy (TEM) showed some intercalation for EOC-17 but much better dispersion for EOC-45 nanocomposites. Differential scanning calorimetry (DSC) showed increased crystallization temperatureTcfor EOC-17 nanocomposite (aggregates acted as nucleation agents) but decreaseTcfor EOC-45 nanocomposite together with greatly influenced melting peak. Accelerated UV aging showed smaller C=O peak for EOC-45 nanocomposites.


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