Enhanced Structural Behavior of Systems Polypropylene-Carbon Nanotubes in Acidic Medium

2014 ◽  
Vol 1613 ◽  
pp. 115-120
Author(s):  
Felipe Avalos-Belmontes ◽  
Miguel Flores-Godina ◽  
Rosa Narro-Cespedes ◽  
Adali Castañeda-Facio ◽  
Martha Castañeda-Flores ◽  
...  

ABSTRACTThe effect of carbon nanotubes (CNTs) on the thermal and chemical stability of polypropylene (PP) when subjected to oxidation in a fuming nitric was evaluated. The effect of CNTs on the crystalline morphology and melting and crystallization temperature of PP was studied. The results shown a thermal stability increased markedly; the decomposition temperature, increased from 293°C for pure PP to 320°C for PP with CNTs. The crystallization temperature increased perceptibly in presence of CNTs. The oxidative degradation with nitric acid produced a reduction in molecular weight; however, this negative effect was less pronounced in the PP compositions with carbon nanoparticles. The morphological changes evaluated with X-ray diffraction showed that the alpha type crystallinity remains, irrespective of the nucleating agent, and the intensity ratios between reflections peaks was taken as an indication of an increasing nucleating efficiency.

2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
F. Avalos-Belmontes ◽  
L. F. Ramos-deValle ◽  
E. Ramírez-Vargas ◽  
S. Sánchez-Valdes ◽  
J. Méndez-Nonel ◽  
...  

The effect of carbon nanofibers (CNFs) and carbon nanotubes (CNTs) on the thermal and chemical stability of polypropylene (PP) when subjected to oxidation in a strong acid medium was studied. The effect of CNFs and CNTs on the crystalline morphology and the melting and crystallization temperatures was also studied. The thermal stability increased markedly; the decomposition temperature, for example, increased from 293∘C for pure PP to 312 and 320∘C for PP with CNFs and CNTs, respectively. The crystallization temperature increased perceptibly with the addition of CNTs or CNFs, from 107∘C for pure PP to 112 and 114∘C for PP with CNFs and CNTs, respectively. The oxidative degradation with nitric acid produced a reduction in molecular weight; however, this negative effect was less pronounced in the PP compositions with carbon nanoparticles. After 8 hours in nitric acid, this reduction was from 141,000 to 68,000 (for pure PP), to 75,000 (for PP-CNFs), and 79,500 (for PP-CNTs). X-ray diffraction showed that the alpha type crystallinity remains, irrespective of the nucleating agent. Finally, the intensity ratio between the (040) (at 16.7∘) and the (110) (at 13.9∘) reflections increased, which was taken as an indication of an increasing nucleating efficiency.


2009 ◽  
Vol 67 ◽  
pp. 197-202 ◽  
Author(s):  
Kuldeep Rana ◽  
Anjan Sil ◽  
Subrata Ray

Carbon nanotubes (CNTs) have been synthesized by chemical decomposition of acetylene gas at 580°C and 650°C using catalyst of LiNi0.5Co0.5O2. The effect of decomposition temperature on structure of the CNTs is that, CNTs grown at 650°C have lower defects concentration and higher crystallinity as compared to that grown at 580°C. The porous anodized aluminum oxide (AAO) template (as substrate), catalyst particles and the CNTs grown were analyzed by FE-SEM. The pore diameter in the template lies in range of 30 - 80 nm. The CNTs have been analyzed by using Raman spectroscopy and X-ray diffraction techniques. The up-shift in G-band of graphitic sheet and larger full width at half maximum of the peak in the Raman spectra of the CNT in comparison to those observed for graphite are indicative of the structural modification. XRD results also indicate the structural modification in CNT based on the fact that d-value becomes 3.42 Å, which is larger than 3.35 Å for graphite. The tube diameters lie in the range of 12 - 50 nm.


2013 ◽  
Vol 832 ◽  
pp. 589-595 ◽  
Author(s):  
N.A. Edama ◽  
A. Sulaiman ◽  
K.H. Ku Hamid ◽  
M.N. Muhd Rodhi ◽  
Mohibah Musa ◽  
...  

This study analyzed the effects of sulphuric acid (H2SO4) treatment on pysico-chemical properties and morphological changes of clay obtained from Sg. Sayong, Perak. The clay was ground and sieved to <150μm and treated with different concentrations of H2SO4. The treatment was completed by refluxing the clay with different concentration of H2SO4 (1M, 5M and 10M ) at 100 °C for 4 hours and followed by calcination at 500 °C for 1 hour. The physic-chemical properties and morphological changes of the untreated and treated clay were compared using Surface Area Analyser, X-Ray Diffraction (XRD), Field Emission Scanning Electron Micrograph (FESEM), X-Ray Diffraction (XRD) and Fourier Transformed Infrared Spectroscopy (FTIR). The results showed that acid treatment of 5M increased the surface area from 25 m2/g to 75 m2/g and the pore volume increased from 0.1518 cc/g to 0.3546 cc/g. The nanopore size of the clay decreased from 24.8 nm to 19.4 nm after treated with acid. This can be explained due to the elimination of the exchangeable cations and generation of microporosity. The results of XRF showed SiO2 increased from 58.34% to 74.52% and Al2O3 reduced from 34.6% to 18.31%. The mineral oxides such as Fe2O3, MgO, CaO, K2O and TiO2 also reduced. This concluded that H2SO4 treatment has led to significant removal of octahedral Al3+, Fe3+ cations and other impurities. In conclusion, this study showed the physico-chemical properties and morphology of Sayong clay were improved once treated with H2SO4 and therefore suggests better supporting material for enzyme immobilization.


2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Patcharanan Junploy ◽  
Titipun Thongtem ◽  
Somchai Thongtem ◽  
Anukorn Phuruangrat

SrSn(OH)6 precursors synthesized by a cyclic microwave radiation (CMR) process were calcined at 900°C for 3 h to form rod-like SrSnO3. Further, the rod-like SrSnO3 and AgNO3 in ethylene glycol (EG) were ultrasonically vibrated to form rod-like Ag/SrSnO3 composites, characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), electron microscopy (EM), Fourier transform infrared (FTIR) spectroscopy, and UV-visible analysis. The photocatalyses of rod-like SrSnO3, 1 wt%, 5 wt%, and 10 wt% Ag/SrSnO3 composites were studied for degradation of methylene blue (MB, C16H18N3SCl) dye under ultraviolet (UV) radiation. In this research, the 5 wt% Ag/SrSnO3 composites showed the highest activity, enhanced by the electron-hole separation process. The photoactivity became lower by the excessive Ag nanoparticles due to the negative effect caused by reduction in the absorption of UV radiation.


2021 ◽  
Vol 21 (11) ◽  
pp. 5673-5680
Author(s):  
Muthukrishnan Francklin Philips ◽  
Jothirathinam Thangarathinam ◽  
Jayakumar Princy ◽  
Cyril Arockiaraj Crispin Tina ◽  
Cyril Arockiaraj Crispin Tina ◽  
...  

The authors report the preparation of the nanocomposite comprising of vanadium pentoxide (V2O5) and selenium (Se) nanoparticles and functionalized multiwalled carbon nanotubes (MWCNTs) (V2O5@Se NPs/MWCNTs). Since Se NPs possesses extraordinary physicochemical properties including larger surface area with higher adsorption capacity, V2O5 NPs were adsorbed onto Se NPs surface through physisorption process (designated as V2O5@Se NPs). The nanocomposite synthesized hydrothermally was evaluated for its antimicrobial activity. The morphology and microstructure of the nanocomposite were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis, respectively. Fourier transform infrared spectroscopy (FTIR) and UV-Visible spectroscopy (UV-Vis) were employed to analyze the spectral properties of nanocomposite. The microbicidal efficacy of nanocomposite was tested against Gram-negative (G-)ZGram-positive (G+) bacteria and fungus. This is the first report on the synthesis of V2O5@Se NPs/MWCNTs nanocomposites by chemical method that showed microbicidal effect on micro-organisms. The thiol (-SH) units facilitates the enrichment of V2O5@Se NPs onto MWCNTs surface. Ultimately, it reflects on the significant antimicrobial activity of V2O5@Se NPs/MWCNTs.


2019 ◽  
Vol 54 (1) ◽  
Author(s):  
Francisco Méndez-Martínez ◽  
Federico González ◽  
Enrique Lima ◽  
Pedro Bosch ◽  
Heriberto Pfeiffer

This work presents the structural characterization and electrical evaluation of Znx-1CuxMn2O4 spinels, which are materials presented as secondary phases into the varistor ceramic systems. Samples were analyzed by X-ray diffraction, solid-state nuclear magnetic resonance, infrared spectroscopy, scanning electron microscopy and impedance spectroscopy. Although, the addition of copper to the ZnMn2O4 spinel did not produce morphological changes, the structure and electrical behaviors changed considerably. Structurally, copper addition induced the formation of partial inverse spinels, and its addition increases significantly the electrical conductivity. Therefore, the formation of Znx-1CuxMn2O4 spinels, as secondary phases into the varistor materials, may compromise significantly the varistor efficiency.   Ceramic, Impedance Spectroscopy, spinel, Varistor, XRD.


2014 ◽  
Vol 2014 ◽  
pp. 1-5
Author(s):  
Daisuke Ogawa ◽  
Ryo Kitaura ◽  
Takeshi Saito ◽  
Shinobu Aoyagi ◽  
Eiji Nishibori ◽  
...  

Thermally fragile tris(η5-cyclopentadienyl)erbium (ErCp3) molecules are encapsulated in single-wall carbon nanotubes (SWCNTs) with high yield. We realized the encapsulation of ErCp3with high filling ratio by using high quality SWCNTs at an optimized temperature under higher vacuum. Structure determination based on high-resolution transmission electron microscope observations together with the image simulations reveals the presence of almost free rotation of each ErCp3molecule in SWCNTs. The encapsulation is also confirmed by X-ray diffraction. Trivalent character of Er ions (i.e., Er3+) is confirmed by X-ray absorption spectrum.


2021 ◽  
pp. 089270572110514
Author(s):  
Himanshu V Madhad ◽  
Dilip V Vasava

Over the years, various types of techniques have been used for the synthesis of nanocomposites. In this work, melamine-based polyamide (PA) was synthesized using a one-pot polycondensation method under mild conditions. carboxyl graphene (CG)/PA nanocomposites (CGMPA) were prepared by CG nanofiller loadings of 1, 3, and 5 wt.% via delamination/adsorption approach. The prepared CGMPA nanocomposites were characterized using different analyses, such as Fourier transform infrared techniques (FTIR), field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), differential scanning calorimetric (DSC), and thermogravimetric analysis (TGA). The effects of the CG on the thermal properties of the CGMPA nanocomposites were significant. The results showed that the melting temperature (Tm) of neat PA and CGMPA were increased from 378°C to 393°C suggested better dispersion of CG in PA matrix. The decomposition temperature of PA was increased from 451°C to 463°C in CGMPA nanocomposites indicates the better thermal stability of PA matrix by addition of CG.


1965 ◽  
Vol 9 ◽  
pp. 170-189 ◽  
Author(s):  
M. Stammler ◽  
R. Bruenner ◽  
W. Schmidt ◽  
D. Orcutt

AbstractThe thermal transformations which take place in solid methyl-substituted ammonium perchlorates have been studied using high-temperature X-ray diffraction and differential thermal analysis techniques. In the temperature range from 20°C to their decomposition temperature (above 300°C), ammonium perchlorate and tetramethyl ammonium perchlorate undergo only one enantiomorphic phase transition, namely at 240 and 340°C (with decomposition), respectively. This I—II transition is ascribed to the beginning of the free rotation of the ClO4− ions. The rotation of the cations, however, begins below room temperature. If the symmetry of the cation is lowered by having both methyl groups and hydrogens arranged around the nitrogen (as in monomethyl, dimethyl, and trimethyl ammonium perchlorates), there is an additional enantiomorphic phase transition. This I—II transformation is ascribed to the rotation of the cations which have, in the partially substituted ions, two sets of non-equivalent symmetry axes (different moments of inertia). The temperatures of transformation are discussed in terms of the space requirements for rotation. Symmetries and cell dimensions of some modifications were determined.


Materials ◽  
2020 ◽  
Vol 13 (12) ◽  
pp. 2716
Author(s):  
Hoang Anh Tuan ◽  
Shinji Hirai ◽  
Shota Inoue ◽  
Alharbi A. H. Mohammed ◽  
Shota Akioka ◽  
...  

This research reports the processability and mechanical properties of silk resins prepared by hot-pressing followed by hot-rolling and then analyzes their thermal and structural properties. The results show that regenerated silk (RS) resins are better suited for hot-rolling than Eri and Bombyx mori silk resins (untreated silk). When hot-rolling at 160 °C with a 50% of reduction ratio, maximum bending strength and Young’s modulus of RS resin reaches 192 MPa and 10.2 GPa, respectively, after pretreatment by immersion in 40 vol% ethanol, and 229 MPa and 12.5 GPa, respectively, after pretreatment by immersion in boiling water. Increased strength of the material is attributed to the increased content of aggregated strands and intramolecular linking of β sheets (attenuated total reflectance Fourier-transform infrared spectroscopy) and higher crystallinity (X-ray diffraction analysis). After hot-pressing and hot-rolling, RS resins have a stable decomposition temperature (297 °C).


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