Spectroscopic and Electrical Studies of Ferrous Sulphate Doped Polyaniline

2012 ◽  
Vol 585 ◽  
pp. 224-227
Author(s):  
Anand Kumar ◽  
Ali Vazid ◽  
Sushil Kumar
Keyword(s):  
Polymer Composites ◽  
Structural Changes ◽  
Metal Salt ◽  
Potassium Dichromate ◽  
Ferrous Sulphate ◽  
Oxidative Polymerization ◽  
Dc Conductivity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Uv Visible

Polyaniline (PANI) has been synthesized by chemical oxidative polymerization technique with potassium dichromate oxidant in aqueous hydrochloric acid medium. After polymerization, the polymer so prepared is doped with ferrous sulphate, a transition metal salt, with tetrahydrofuran and water as solvents. The undoped/doped samples were characterized by various techniques such as UV-visible spectroscopy, FTIR spectroscopy, X-ray diffraction and dc conductivity measurements. UV-visible absorption studies revealed the presence of cation/polaron transitions and the presence of direct optical transitions. FTIR studies provide information regarding structural changes in the backbone of PANI with doping concentration. X-ray diffraction patterns of powdered polymer composites showed amorphous nature as mostly conducting polymers exhibit. The dc conductivity of PANI-ferrous sulphate composites were measured by two probe method in pellet form at room temperature (300 K) and found to increase with temperature showing the semiconductor behavior of synthesized polymer composites

scholarly journals Studies on Synthesis, Characterization and Transport Properties of Ta2O5 Doped Polyaniline Composites

2021 ◽  
Vol 7 (1) ◽  
pp. 942-945
Author(s):  
Nagajyoti ◽  
Kalayne Sangshetty
Keyword(s):  
Structural Changes ◽  
Morphological Changes ◽  
Oxidative Polymerization ◽  
Average Crystallite Size ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Doped Polyaniline ◽  
Polyaniline Composites ◽  
Composite Samples

Polyaniline (PANI) and PANI/Ta2O5 composite samples were prepared using chemical oxidative polymerization technique in the presence of hydrochloric acid (HCl) at room temperature. The effect of Ta2O5 on surface morphology and structural changes have been investigated and evaluated by X-ray diffraction (XRD) and scanning electron microscope (SEM) techniques. The XRD pattern of the PANI and PANI/Ta2O5 confirm the formation of PANI and its composite. The average crystallite size of the PANI is 2.86 nm which is increased to 46.80 nm when Ta2O5 was doped in the PANI matrix. SEM micrographs of the composite confirm the morphological changes in the composite materials. In the electrical conductivity studies, ac conductivity was carried as function of frequency and dc conductivity was studied as a function of temperature. Further to describe the dielectric properties of the PANI and composite, dielectric constant and dielectric loss was studied as a function of frequency.

Studies on Polyaniline/Silver Molybdate Nanocomposites

2014 ◽  
Vol 13 (01) ◽  
pp. 1450002 ◽  
Author(s):  
K. Jacinth Mispa ◽  
P. Subramaniam ◽  
R. Murugesan
Keyword(s):  
Oxidative Polymerization ◽  
Hydrothermal Process ◽  
Photoluminescence Spectra ◽  
X Ray Diffraction ◽  
X Ray ◽  
Silver Molybdate ◽  
Visible Spectra ◽  
Ft Ir ◽  
Uv Visible

Silver molybdate nanoparticles were successfully prepared by the hydrothermal process. Polyaniline–silver molybdate nanocomposites were prepared by in situ chemical oxidative polymerization technique. Silver molybdate nanoparticles and the polymer samples were characterized by conductivity studies, Fourier transform infrared spectra (FT-IR), UV-visible spectra, photoluminescence spectra, X-ray diffraction (XRD), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). The electrical conductivity of PANI- Cl - increases when doped with silver molybdate nanoparticles and follows the percolation threshold.

scholarly journals A nearly on-axis spectroscopic system for simultaneously measuring UV–visible absorption and X-ray diffraction in the SPring-8 structural genomics beamline

2016 ◽  
Vol 23 (1) ◽  
pp. 334-338 ◽  
Author(s):  
Miyuki Sakaguchi ◽  
Tetsunari Kimura ◽  
Takuma Nishida ◽  
Takehiko Tosha ◽  
Hiroshi Sugimoto ◽  
...  
Keyword(s):  
Active Sites ◽  
Structural Changes ◽  
Spectroscopic Analysis ◽  
Uv Light ◽  
X Ray Diffraction ◽  
Visible Absorption ◽  
X Ray ◽  
Protein Active Sites ◽  
On Line ◽  
Uv Visible

UV–visible absorption spectroscopy is useful for probing the electronic and structural changes of protein active sites, and thus the on-line combination of X-ray diffraction and spectroscopic analysis is increasingly being applied. Herein, a novel absorption spectrometer was developed at SPring-8 BL26B2 with a nearly on-axis geometry between the X-ray and optical axes. A small prism mirror was placed near the X-ray beamstop to pass the light only 2° off the X-ray beam, enabling spectroscopic analysis of the X-ray-exposed volume of a crystal during X-ray diffraction data collection. The spectrometer was applied to NO reductase, a heme enzyme that catalyzes NO reduction to N2O. Radiation damage to the heme was monitored in real time during X-ray irradiation by evaluating the absorption spectral changes. Moreover, NO binding to the heme was probedviacaged NO photolysis with UV light, demonstrating the extended capability of the spectrometer for intermediate analysis.

In Situ Intercalation/Polymerization of Melanin into Vanadium Pentoxide

1999 ◽  
Vol 576 ◽  
Author(s):  
H. P. Oliveira ◽  
C. L. P. S. Zanta ◽  
A. C. Galina ◽  
C. F. O. Graeff
Keyword(s):  
Oxidative Polymerization ◽  
Esr Spectra ◽  
Dc Conductivity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Oxidation Reduction ◽  
The Stability ◽  
Intercalation Polymerization ◽  
Inorganic Layers

ABSTRACTIn this work, intercalated material was prepared consisting of a regular interchange of organic/inorganic layers. The products were obtained by reacting 3,4-dihidroxi-fenilalanina (DL-DOPA) in a solution with V2O5.nH2O gel, which suffered an oxidative polymerization/intercalation process, forming a film with a dark blue metallic color. The films were characterized using UV\Vis transmission spectroscopy, FTLR, ESR, X-ray diffraction, dc conductivity, and cyclic voltammetry. The X-ray diffractograms indicate that the lamellar structure of the V2O5 is preserved but the inter-planar space increase from 1.18 nm to 1.38 nm. The FTIR and ESR spectra confirms that the V2O5 structure is preserved, however the presence of melanin induces the reduction of Vv ions to Viv. The increase in the inter-planar spacing is observed to increase the stability and reproducibility of the electrochemical insertion/de-insertion of Li+. This increase in stability is also observed in the electrochromic properties of the film, which are fully reproducible even after more than 60 oxidation-reduction cycles. The melanin affects also the activation energy of the dc conductivity which changes from 0.35 eV to 0.20 eV.

Chemical modification of the bacterial wall to determine sites of metal deposition

1978 ◽  
Vol 36 (2) ◽  
pp. 350-351
Author(s):  
T. J. Beveridge
Keyword(s):  
Electron Scattering ◽  
Metal Salt ◽  
Metal Deposition ◽  
Suitable Model ◽  
X Ray Diffraction ◽  
Subtilis Cell ◽  
Thin Sections ◽  
X Ray ◽  
Section Data ◽  
Metal Impregnation

The Bacillus subtilis cell wall provides a protective sacculus about the vital constituents of the bacterium and consists of a collection of anionic hetero- and homopolymers which are mainly polysaccharidic. We recently demonstrated that unfixed walls were able to trap and retain substantial amounts of metal when suspended in aqueous metal salt solutions. These walls were briefly mixed with low concentration metal solutions (5mM for 10 min at 22°C), were well washed with deionized distilled water, and the quantity of metal uptake (atomic absorption and X-ray fluorescence), the type of staining response (electron scattering profile of thin-sections), and the crystallinity of the deposition product (X-ray diffraction of embedded specimens) determined.Since most biological material possesses little electron scattering ability electron microscopists have been forced to depend on heavy metal impregnation of the specimen before obtaining thin-section data. Our experience with these walls suggested that they may provide a suitable model system with which to study the sites of reaction for this metal deposition.

Microstructure and Physical Properties of Clay-Polymer Composites

2000 ◽  
Vol 628 ◽  
Author(s):  
T.N. Blanton ◽  
D. Majumdar ◽  
S.M. Melpolder
Keyword(s):  
Composite Materials ◽  
Physical Properties ◽  
Polymer Composites ◽  
Basal Plane ◽  
X Ray Diffraction ◽  
X Ray ◽  
Layered Clay

ABSTRACTClay-polymer nanoparticulate composite materials are evaluated by the X-ray diffraction technique. The basal plane spacing provided information about the degree of intercalation and exfoliation of the 2: 1 layered clay structure. Both intercalation and exfoliation are controlled by the identity of the polymer and the clay:polymer ratio.

Hydrolytic products of Fe(III) after oxidation of Fe(II) by chlorate

1982 ◽  
Vol 47 (4) ◽  
pp. 1069-1077 ◽  
Author(s):  
Karel Mádlo ◽  
František Hanousek ◽  
Antonín Petřina ◽  
Jaroslav Tláskal
Keyword(s):  
Electron Microscopy ◽  
Ir Spectroscopy ◽  
Chemical Analysis ◽  
Ferrous Sulphate ◽  
Reaction Medium ◽  
Potassium Chlorate ◽  
X Ray Diffraction ◽  
X Ray

Ferrous sulphate was oxidized by potassium chlorate in the pH region 2-7 and at temperatures ranging from 298.1 to 323.1 K and various hydrolytic products of Fe(III) were separated and indentified. The separated solid ferric products were analyzed using a combination of the chemical analysis, IR spectroscopy, X-ray diffraction, and electron microscopy. The following substances were found as major components of the products: Fe2O3.n H2O ("ferric gel"), Fe2O3.n H2O with bound SO2-4 ions ("sulphogel"), α-FeO(OH), γ-FeO(OH) and Fe3O4. Their amount depends particularly on the pH temperature of the reaction medium.

scholarly journals High temperature structural study of decagonal Al-Cu-Rh quasicrystal.

2014 ◽  
Vol 70 (a1) ◽  
pp. C94-C94
Author(s):  
Pawel Kuczera ◽  
Walter Steurer
Keyword(s):  
Structural Changes ◽  
Configurational Entropy ◽  
Lattice Vibrations ◽  
X Ray Diffraction ◽  
Stabilization Mechanism ◽  
X Ray ◽  
Comparative Structure ◽  
The Stability

The structure of d(ecagonal)-Al-Cu-Rh has been studied as a function of temperature by in-situ single-crystal X-ray diffraction in order to contribute to the discussion on energy or entropy stabilization of quasicrystals (QC) [1]. The experiments were performed at 293 K, 1223 K, 1153 K, 1083 K, and 1013 K. A common subset of 1460 unique reflections was used for the comparative structure refinements at each temperature. The results obtained for the HT structure refinements of d-Al-Cu-Rh QC seem to contradict a pure phasonic-entropy-based stabilization mechanism [2] for this QC. The trends observed for the ln func(I(T1 )/I(T2 )) vs.|k⊥ |^2 plots indicate that the best on-average quasiperiodic order exists between 1083 K and 1153 K, however, what that actually means is unclear. It could indicate towards a small phasonic contribution to entropy, but such contribution is not seen in the structure refinements. A rough estimation of the hypothetic phason instability temperature shows that it would be kinetically inaccessible and thus the phase transition to a 12 Å low T structure (at ~800 K) is most likely not phason-driven. Except for the obvious increase in the amplitude of the thermal motion, no other significant structural changes, in particular no sources of additional phason-related configurational entropy, were found. All structures are refined to very similar R-values, which proves that the quality of the refinement at each temperature is the same. This suggests, that concerning the stability factors, some QCs could be similar to other HT complex intermetallic phases. The experimental results clearly show that at least the ~4 Å structure of d-Al-Cu-Rh is a HT phase therefore entropy plays an important role in its stabilisation mechanism lowering the free energy. However, the main source of this entropy is probably not related to phason flips, but rather to lattice vibrations, occupational disorder unrelated to phason flips like split positions along the periodic axis.

Optical properties of anatase TiO2 films modified by N ion implantation

2012 ◽  
Vol 90 (1) ◽  
pp. 39-43 ◽  
Author(s):  
X. Xiang ◽  
D. Chang ◽  
Y. Jiang ◽  
C.M. Liu ◽  
X.T. Zu
Keyword(s):  
Thin Films ◽  
Ion Implantation ◽  
Photoelectron Spectroscopy ◽  
Radio Frequency Magnetron Sputtering ◽  
X Ray Diffraction ◽  
X Ray ◽  
Atomic Force ◽  
Light Region ◽  
Uv Visible ◽  
Substrate Temperatures

Anatase TiO2 thin films are deposited on K9 glass samples at different substrate temperatures by radio frequency magnetron sputtering. N ion implantation is performed in the as-deposited TiO2 thin films at ion fluences of 5 × 1016, 1 × 1017, and 5 × 1017 ions/cm2. X-ray diffraction, atomic force microscope, X-ray photoelectron spectroscopy (XPS), and UV–visible spectrophotometer are used to characterize the films. With increasing N ion fluences, the absorption edges of anatase TiO2 films shift to longer wavelengths and the absorbance increases in the visible light region. XPS results show that the red shift of TiO2 films is due to the formation of N–Ti–O compounds. As a result, photoactivity is enhanced with increasing N ion fluence.

Investigations of Actinide Metals and Compounds under Pressure Provide Important Insights into Bonding and Chemistry

2003 ◽  
Vol 802 ◽  
Author(s):  
R. G. Haire ◽  
S. Heathman ◽  
T. Le Bihan ◽  
A. Lindbaum ◽  
M. Iridi
Keyword(s):  
Structural Changes ◽  
Chemical Properties ◽  
X Ray Diffraction ◽  
Interatomic Distances ◽  
X Ray ◽  
Effect Of Pressure ◽  
Electronic Configurations ◽  
5F Electrons ◽  
Actinide Series ◽  
Alloys And Compounds

ABSTRACTOne effect of pressure on elements and compounds is to decease their interatomic distances, which can bring about dramatic perturbations in their electronic nature and bonding, which can be reflected in changes in physical and/or chemical properties. One important issue in the actinide series of elements is the effect of pressure on the 5f-electrons. We have probed changes in electronic behavior with pressure by monitoring structure by X-ray diffraction, and have studied several actinide metals and compounds from thorium through einsteinium. These studies have employed angle dispersive diffraction using synchrotron radiation, and energy dispersive techniques via conventional X-ray sources. The 5f-electrons of actinide metals and their alloys are often affected significantly by pressure, while with compounds, the structural changes are often not linked to the involvement of 5 f-electron. We shall present some of our more recent findings from studies of selected actinide metals, alloys and compounds under pressure. A discussion of the results in terms of the changes in electronic configurations and bonding with regard to the element's position in the series is also addressed.

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