Preparation and Uranium Sorption Performance of Amidoximated Polyacrylonitrile/Organobentonite Nano Composite

2012 ◽  
Vol 476-478 ◽  
pp. 2317-2322 ◽  
Author(s):  
Jiang Nan Shen ◽  
Jie Yu ◽  
Yue Xia Chu ◽  
Yong Zhou ◽  
Wei Jun Chen
Keyword(s):  
Absorption Band ◽  
In Situ Polymerization ◽  
Ion Concentration ◽  
Polymerization Temperature ◽  
X Ray Diffraction ◽  
Nano Composite ◽  
X Ray ◽  
Ft Ir ◽  
Intercalation Polymerization

Polyacrylonitrile/montmorillonite (PAN/MMT) nanocomposite with amidoxime functionality was prepared from acrylonitrile monomer(AN) and montmorillonite(MMT) through in-situ intercalation polymerization. Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction patter (XRD) were employed to characterize the obtained Na-MMT、Organ-MMT、PAN/MMT、APAN/MMT. Effects of preparing conditions of APAN/MMT on adsorption of uranium were investigated. The FT-IR spectra show that the new absorption band at 1653 cm-1( ) appears and the absorption band at 2243 cm-1(-CN) disappears on the spectrum of APAN/MMT, it indicates that the AN and MMT are successfully polymerized by in-situ polymerization and the PAN/MMT is amidoxime functionalized. The APAN/MMT nanocomposite completely lose the X-ray diffraction. The adsorption results show that the obtained APAN-MMT gives uranium adsorption capacity of 3.06 mg.g-1 under following conditions: uranium ion concentration of 10 mg/L, AM mass concentration of 80.0%, initiator of 4.5%, polymerization temperature of 70 °C，polymerization time of 3 h, pH of 7 and amidoxime functionalized reaction time of 2 h.

scholarly journals Thermal and electrical properties of polyimide/PANI nanofiber composites prepared via in situ polymerization

2018 ◽  
Vol 36 (2) ◽  
pp. 283-287
Author(s):  
Aseel A. Kareem
Keyword(s):  
In Situ Polymerization ◽  
Composite Films ◽  
Nanocomposite Films ◽  
X Ray Diffraction ◽  
Nanofiber Composite ◽  
X Ray ◽  
Thermal And Electrical Properties ◽  
Ft Ir ◽  
Thermal Stability Of

Abstract Polyimide/polyaniline nanofiber composites were prepared by in situ polymerization with various weight percentages of polyaniline (PANI) nanofibers. X-ray diffraction (XRD) and Fourier transform infrared spectra (FT-IR), proved the successful preparation of PANI nanofiber composite films. In addition, thermal stability of PI/PANI nanofiber composites was superior relative to PI, having 10 % gravimetric loss in the range of 623 °C to 671 °C and glass transition temperature of 289 °C to 297 °C. Furthermore, the values of the loss tangent tanδ and AC conductivity σAC of the nanocomposite films were notably higher than those of pure polyimide. The addition of 5 wt.% to 15 wt.% PANI nanofiber filler enhanced the activation energy of PI composites from 0.37 eV to 0.34 eV.

scholarly journals Synthesis and Characterization of New Polyimide/Organoclay Nanocomposites Containing Benzophenone Moieties in the Main Chain

2017 ◽  
Vol 57 (2) ◽  
Author(s):  
Khalil Faghihi ◽  
Mostafa Ashouri ◽  
Akram Feyzi
Keyword(s):  
Main Chain ◽  
In Situ Polymerization ◽  
Clay Content ◽  
Nanocomposite Films ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

<p>A series of nanocomposites consist of organic polyimide and organo-modified clay content varying from 0 to 5 wt%, were successfully prepared by in situ polymerization. Polyimide used as a matrix of nanocomposite was prepared through the reaction of 1,4-bis [4-aminophenoxy] butane (APB) and 3،3΄،4،4΄-benzophenone tetra carboxylic dianhydride (BTDA) in N,N-dimethylacetamide (DMAc). The resulting nanocomposite films were characterized by FT-IR spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA).</p>

scholarly journals In-Situ Preparation of Conducting Polymers/Copper (II)-Maghnite Clay Nanocomposites

2017 ◽  
Vol 14 (2) ◽  
pp. 204-211 ◽  
Author(s):  
Fatima Zeggai ◽  
Mohammed Belbachir ◽  
Aicha Hachmaoui
Keyword(s):  
Conducting Polymers ◽  
In Situ Polymerization ◽  
Ammonium Persulfate ◽  
Clay Nanocomposites ◽  
X Ray Diffraction ◽  
X Ray ◽  
In Situ Preparation ◽  
Ft Ir ◽  
The Fourier Transform

In this work we report a simple way for the conducting polymer nanocomposites synthesis using on algerian hydrophilic natural Montmorillonite (MMT) nanoclay named Maghnite (Mag) as dopant. The electrochemical properties study of the following conducting polymers: poly(4-aminobenzylamine) (P4ABA) and polyaniline (PANI) nanocomposites with copper maghnite (Mag-Cu) were successfully prepared by In-Situ polymerization, in presence of inorganic nanolayers of clay, and oxidizing agent ammonium persulfate. The synthesis of copolymers was developed at different feed mole fractions of monomer. The products were characterized by the Fourier transform Infrared (FT-IR), the ultraviolet-visible (UV–vis) spectroscopies and X-ray diffraction (XRD). The results showed that the in-situ polymerization produced real nanocomposites containing aniline and 4-aminobenzylamine units.

Synthesis and Characterization of the PANI/ITO Conducting Nanocomposites

2010 ◽  
Vol 663-665 ◽  
pp. 542-545 ◽  
Author(s):  
Bing Jie Zhu ◽  
Xin Wei Wang ◽  
Mei Fang Zhu ◽  
Qing Hong Zhang ◽  
Yao Gang Li ◽  
...  
Keyword(s):  
Doping Concentration ◽  
In Situ Polymerization ◽  
Synthesis And Characterization ◽  
Conductivity Measurements ◽  
X Ray Diffraction ◽  
X Ray ◽  
Maximum Conductivity ◽  
Scanning Electron

The PANI/ITO conducting nanocomposites have been synthesized by in-situ polymerization. The obtained nanocomposites were characterized by X-ray diffraction pattern, scanning electron microscopy and Fourier transform infrared. Electrical conductivity measurements on the samples pressed into pellets showed that the maximum conductivity attained 2.0 ± 0.05 S/cm for PANI/ITO nanocomposites, at ITO doping concentration of 10 wt%. The results of the present work may provide a simple, rapid and efficient approach for preparing PANI/ITO nanocomposites.

Morphology of Polyethylene/Montmorillonite Nanocomposites Prepared by In Situ Polymerization

2013 ◽  
Vol 457-458 ◽  
pp. 244-247
Author(s):  
Min Li ◽  
Li Guang Xiao ◽  
Hong Kai Zhao
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
In Situ Polymerization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Reflection Peak ◽  
Basal Reflection ◽  
Scanning Electron

Polyethylene/montmorillonite (PE/MMT) nanocomposites were prepared by in situ polymerization. The morphology of MMT/MgCl2/TiCl4 catalyst and PE/MMT nanocomposites was investigated by scanning electron microscopy (SEM). It can be seen that MMT/MgCl2/TiCl4 catalyst remained the original MMT sheet structures and many holes were found in MMT and the morphology of PE/MMT nanocomposites is part of the sheet in the form of existence, as most of the petal structure. X-ray diffraction (XRD) and transmission electron microscopy (TEM) were carried out to characterize all the samples. XRD results reveal that the original basal reflection peak of PEI1 and PEI2 disappears completely and that of PEI3 become very weak. MMT/MgCl2/TiCl4 catalyst was finely dispersed in the PE matrix. Instead of being individually dispersed, most layers were found in thin stacks comprising several swollen layers.

Preparation of Hydrophobic CaCO3-Wood Composite In Situ

2010 ◽  
Vol 113-116 ◽  
pp. 1712-1715
Author(s):  
Cheng Yu Wang ◽  
Chang Yu Liu ◽  
Jian Li
Keyword(s):  
Mechanical Properties ◽  
Organic Substrate ◽  
Dodecanoic Acid ◽  
Wood Composite ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Contact Angle Analysis ◽  
Double Diffusive

The preparation of hydrophobic CaCO3-wood composite through a double-diffusive method using dodecanoic acid as organic substrate is demonstrated. The product was characterized by the contact angle analysis, X-ray diffraction (XRD), fourier transform infrared spectroscopy (FT-IR) and scanning electron microscope (SEM). The mechanical properties of the product were measured. The results show that the synthesized CaCO3 fills in the wood cell and covers the surface of wood. The CaCO3-wood composite is hydrophobic. The mechanical properties of wood composite have significantly increased.

scholarly journals “PdO vs. PtO”—The Influence of PGM Oxide Promotion of Co3O4 Spinel on Direct NO Decomposition Activity

Catalysts ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 62 ◽  
Author(s):  
Gunugunuri K. Reddy ◽  
Torin C. Peck ◽  
Charles A. Roberts
Keyword(s):  
Photoelectron Spectroscopy ◽  
No Decomposition ◽  
Single Element ◽  
X Ray Diffraction ◽  
X Ray ◽  
Promotional Effect ◽  
Ft Ir ◽  
Temperature Programmed ◽  
Thermal Stability Of

Direct decomposition of NO into N2 and O2 (2NO→N2 + O2) is recognized as the “ideal” reaction for NOx removal because it needs no reductant. It was reported that the spinel Co3O4 is one of the most active single-element oxide catalysts for NO decomposition at higher reaction temperatures, however, activity remains low below 650 °C. The present study aims to investigate new promoters for Co3O4, specifically PdO vs. PtO. Interestingly, the PdO promoter effect on Co3O4 was much greater than the PtO effect, yielding a 4 times higher activity for direct NO decomposition at 650 °C. Also, Co3O4 catalysts with the PdO promoter exhibit higher selectivity to N2 compared to PtO/Co3O4 catalysts. Several characterization measurements, including X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), H2-temperature programmed reduction (H2-TPR), and in situ FT-IR, were performed to understand the effect of PdO vs. PtO on the properties of Co3O4. Structural and surface analysis measurements show that impregnation of PdO on Co3O4 leads to a greater ease of reduction of the catalysts and an increased thermal stability of surface adsorbed NOx species, which contribute to promotion of direct NO decomposition activity. In contrast, rather than remaining solely as a surface species, PtO enters the Co3O4 structure, and it promotes neither redox properties nor NO adsorption properties of Co3O4, resulting in a diminished promotional effect compared to PdO.

MECHANICAL PROPERTIES OF A POLYURETHANE/MONTMORILLONITE NANOCOMPOSITE FEATURING ORGANOMODIFICATION SYNTHESIZED VIA IN SITU POLYMERIZATION

2015 ◽  
Vol 88 (1) ◽  
pp. 138-146 ◽  
Author(s):  
Rouhollah Bagheri ◽  
Reza Darvishi
Keyword(s):  
Mechanical Properties ◽  
In Situ Polymerization ◽  
Xrd Analysis ◽  
Silicate Layer ◽  
X Ray Diffraction ◽  
X Ray ◽  
End Groups ◽  
Layer Sample ◽  
Silicate Layers

ABSTRACT In this study, polyurethane (PU)/organomodified montmorillonite (cloisite®30B) is synthesized via in situ polymerization by reaction of an ether-based prepolymer with the isocyanate end groups and adiamine chain extender (4, 4-methylene-bis(2-chloroaniline)) in the presence of different amounts of nanoparticles dispersed in the prepolymer matrix by an ultrasonic mixer for 1 h. The synthesized polymers are cast on a pretreated carbon steel sheet and cured at 120 °C in an oven. The PU and its composites have been characterized by using Fourier transform infrared spectroscopy, X-ray diffraction (XRD), and mechanical testing. The XRD analysis of the cured samples containing 1 to 3 wt% cloisite30B showed intercalation segments in the silicate layers and exfoliation for 0.5 wt% nanoparticles. The highest mechanical properties were obtained using the cured exfoliated silicate layer sample. A twofold increase in the ultimate tensile strength and a 2.3 times increase in the adhesion strength were found for 0.5 wt% organoclay/PU as compared with that of pure PU. In addition, the exfoliated structure sample exhibited a 16% reduction in abrasion compared with that of pure PU.

In Situ Polymerization and Characterization of Poly(ε-caprolactone)/Layered Double Hydroxide Nanocomposites

2012 ◽  
Vol 557-559 ◽  
pp. 371-374
Author(s):  
Lian Liu ◽  
Teng Yu ◽  
Pei Wang ◽  
Guang Shuo Wang
Keyword(s):  
Layered Double Hydroxide ◽  
In Situ Polymerization ◽  
X Ray Diffraction ◽  
Visible Spectroscopy ◽  
X Ray ◽  
Uv Visible ◽  
Absorbance Peak ◽  
Double Hydroxide

Nanocomposites of poly(ε-caprolactone) (PCL) and layered double hydroxide (LDH) were prepared by in situ polymerization at low LDHs loadings in this work. The resultants were characterized by FTIR spectroscopy, X-ray diffraction (XRD), differential scanning calorimeter (DSC) and UV-visible spectroscopy (UV-vis). FTIR showed that the PCL/LDHs nanocomposites were prepared successfully by in situ polymerization and XRD spectra showed that the crystal structure did not change greatly in the presence of LDHS. DSC results confirmed that LDHs could act as nucleating agents. UV-vis spectra showed that LDHs had stronger absorbance peak than LDH. Moreover, the PCL/LDHs nanocomposites had strong anti-ultraviolet effect by introduction of LDHs into polymer matrix.

IN SITU SYNTHESIS, CHARACTERIZATION AND FREQUENCY DEPENDENT AC CONDUCTIVITY OF POLYANILINE/CoFe2O4 NANOCOMPOSITES

2011 ◽  
Vol 01 (03) ◽  
pp. 357-362 ◽  
Author(s):  
G. D. PRASANNA ◽  
H. S. JAYANNA
Keyword(s):  
Ac Conductivity ◽  
Room Temperature ◽  
In Situ Polymerization ◽  
In Situ Synthesis ◽  
Electron Micrograph ◽  
Frequency Range ◽  
X Ray Diffraction ◽  
Scanning Electron Micrograph ◽  
X Ray

The polyaniline (PANI)/ CoFe2O4 nanocomposites were prepared by an In Situ polymerization of aniline in an aqueous solution. The composites were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectrum,thermogravimetric analysis (TGA) and scanning electron micrograph (SEM). The AC conductivity and dielectric properties of these composites were investigated in the frequency range 1 kHz–10 MHz at room temperature. The AC conductivity was found to be constant up to 1 MHz and thereafter it increases steeply and it was observed maximum for the PANI with 60 wt% of CoFe2O4 nanocomposite. At lower frequencies the values of dielectric constant is maximum for pure CoFe2O4 nanoparticles.

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