Sunajadevi, K R; Sugunan, S(Elsevier, October , 2004)
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Abstract:
Chromia loaded sulfated titania has been synthesized via sol–gel route with different chromia loadings. These catalysts are characterized using conventional techniques such as XRD analysis, FTIR analysis, surface area and pore volume measurements, EDX, SEM and UV–Vis diffuse reflectance spectral analysis. Acidity is measured using spectrophotometric monitoring of adsorption of perylene, thermogravimetric desorption of 2,6-dimethylpyridine and temperature programmed desorption of ammonia. Activity studies are done in the liquid phase. It has been concluded that Lewis acid sites are responsible for the benzylation of arenes with benzyl chloride.
A series of rare-earth neodymia supported vanadium oxide catalysts with various V205 loadings ranging from 3 to 15 wt.% were prepared
by the wet impregnation method using ammonium metavanadate as the vanadium precursor. The nature of vanadia species formed on the
support surface is characterized hy a series of different physicochemical techniques like X-ray diffraction (XRD). Fourier transform infrared
spectroscopy (FTIR). BET surface area, diffuse reflectance UV-vis spectroscopy (DR UV-vis), thermal analysis (TG-DTG/DTA) and SEM.
The acidity of the prepared systems were verified by the stepwise temperature programmed desorprion of ammonia (NH3-TPD) and found that
the total acidity gets increased with the percentage of vanadia loading. XRD and FT1R results shows the presence of surface dispersed vanadyl
species at lower loadings and the formation of higher vanadate species as the percentage composition of vanadia is increased above 9 wt.%.
The low surface area of the support. calcination temperature and the percentage of vanadia loading are found to influence the formation of
higher vanadia species. The catalytic activity of the V205-Nd203 catalysts was probed in the liquid phase hydroxylation of phenol and the
result show that the present catalysts are active at lower vanadia concentrations.
Mohammed Yusuff, K K; Anas, K(Elsevier, Applied Catalysis A :General 264 (2004) 213–217, December 25, 2003)
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CoMo/gama-Al2O3 catalysts for hydrodesulphurisation activity were prepared by making use of the molecular designed dispersion (MDD)
method. Molybdenum and cobalt pyrrolidine-N-carbodithioate (Pydtc) complexes were used for the incorporation of metals on the support.
The catalysts were characterized by elemental analysis, low temperature oxygen chemisorption, temperature programmed reduction (TPR)
and laser Raman spectroscopy. The hydrodesulphurisation activity of all the catalysts were carried out and results were compared with those
of the catalysts prepared through the conventional method. Higher molybdenum dispersion, smaller molybdenum clusters, lower reduction
temperature of catalyst and better hydrodesulphurisation activity were observed for the catalysts prepared through the MDD method
The title reaction was undertaken to establish the interaction between amantadine and molybdate at physiological pH. Identical FTIR spectra, TG-DTA curves and CHN data of the complexes formed from three solutions at pH 1.5, 7.4 and 8.0 indicate that the same complex was formed at all the three pHs. The FTIR spectrum shows shift in peaks corresponding to primary amino group of the drug due to coordination to molybdate. An octahedral geometry is assigned to the complex. The kinetics of the complexation has been studied at low concentrations of the reactants using UV-visible spectrophotometry. At pH 7.4, the initial rate varies linearly with [molybdate]. A plot of initial rate versus [drug] is linear passing through origin. These results indicate that the drug and molybdate react at pH 7.4 even at low concentrations. At pH 1.5, the rate increases linearly with increase in [drug] but decreases with [molybdate]. The effect of pH and ionic strength on the rate of the reaction has also been studied. A suitable mechanism has been proposed for the reaction. Reaction between the drug and molybdate even at low concentrations and the fact that the amino group of amantadine required to be free for its function as antiviral, is bound to molybdate in the complex suggests that simultaneous administration of the drug and molybdate supplements should be avoided.
Pazhoor Bijumon, Varghese; Mohanan, P; Mailadil, Thomas Sebastian(The Japan Society of Applied Physics, 2002)
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Microwave ceramic dielectric materials Ca5Nb2TiO12 and Ca5Ta2TiO12 have been prepared by a conventional solid-state
ceramic process. The structure was studied by X-ray diffraction and the dielectric properties were characterized at microwave
frequencies. The ceramics posses a relatively high dielectric constant, very low dielectric loss (Q5 x f > 30000GHz) and
small temperature variation of resonant frequency. These materials are potential candidates for dielectric resonator
applications in microwave integrated circuits. [DOI: 10. 1 143/JJAP.41.3834]
Dielectric ceramics based on solid solution phases of [RE1_x= REr]TiNb06, where REI_s = Nd, Pr, Sm and RE' = Dy, Gd and Y, were prepared by the conventional solid-state ceramic route for values of x. The ceramic samples are characterized by X-ray diffraction and microwave methods. Ceramics based on RE (Pr, Nd and Sm) belonging to aeschynite group shows positive value of Tf and those based on RE (Gd, Dy and Y) belonging to euxenite group show negative value of r f. The solid solution phases between the aeschynite and the euxenite group shows intermediate dielectric constant and r f values. The results indicate the possibility of tailoring the dielectric properties by varying the composition of the solid solution phases. The range of solid solubility of euxenite in aeschenite and aeschenite
in euxenite are different for different rare earth ions
Mohammed Yusuff, K K; Manju, Sebastian; Arun, Vasudevan; Robinson, P P; Leeju, Pally; Digna, Varghese; Varsha, Gopalakrishnan(Taylor & Francis, Journal of Coordination Chemistry, October 15, 2009)
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Abstract:
The mononuclear cobalt(II) complex [CoL2] H2O (where HL is quinoxaline-2-carboxalidine-
2-amino-5-methylphenol) has been prepared and characterized by elemental analysis, conductivity
measurement, IR, UV-Vis spectroscopy, TG-DTA, and X-ray structure determination.
The crystallographic study shows that cobalt(II) is distorted octahedral with each tridentate
NNO Schiff base in a cis arrangement. The crystal exhibits a 2-D polymeric structure parallel to
[010] plane, formed by O-H...N and O-H... O intermolecular hydrogen bonds and pye
stacking interactions, as a racemic mixture of optical enantiomers. The ligand is a Schiff base
derived from quinoxaline-2-carboxaldehyde
Reena Mary, A P; Narayanan, T N; Vijutha, Sunny; Sakthikumar, D; Yasuhiko, Yoshida; Joy, P A; Anantharaman, M R(Springer, 2010)
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Bio-compatible magnetic fluids having high
saturation magnetization find immense applications in
various biomedical fields. Aqueous ferrofluids of superparamagnetic
iron oxide nanoparticles with narrow size
distribution, high shelf life and good stability is realized by
controlled chemical co-precipitation process. The crystal
structure is verified by X-ray diffraction technique. Particle
sizes are evaluated by employing Transmission electron
microscopy. Room temperature and low-temperature magnetic
measurements were carried out with Superconducting
Quantum Interference Device. The fluid exhibits good
magnetic response even at very high dilution (6.28 mg/cc).
This is an advantage for biomedical applications, since only
a small amount of iron is to be metabolised by body organs.
Magnetic field induced transmission measurements carried
out at photon energy of diode laser (670 nm) exhibited
excellent linear dichroism. Based on the structural and
magnetic measurements, the power loss for the magnetic nanoparticles under study is evaluated over a range of
radiofrequencies.
Bejoy, Thomas; Prathapan, Sreedharan; Sugunan, Sankaran(Elsevier, May , 2005)
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The synthesis of dimethyl acetals of carbonyl compounds such as cyclohexanone, acetophenone, and benzophenone has successfully been carried out by the reaction between ketones and methanol using different solid acid catalysts. The strong influence of the textural properties of the catalysts such as acid amount and adsorption properties (surface area and pore volume) determine the catalytic activity. The molecular size of the reactants and products determine the acetalization ability of a particular ketone. The hydrophobicity of the various rare earth exchanged Mg–Y zeolites, K-10 montmorillonite clay, and cerium exchanged montmorillonite (which shows maximum activity) is more determinant than the number of active sites present on the catalyst. The optimum number of acidic sites as well as dehydrating ability of Ce3+-montmorillonite and K-10 montmorillonite clays and various rare earth exchanged Mg–Y zeolites seem to work well in shifting the equilibrium to the product side.
Muhammad Abdul Jamal, E; Joy, P A; Anantharaman, M R; Philip, Kurian(Elsevier, January , 2009)
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Nanocomposites based on natural rubber and nano-sized nickelwere synthesized by incorporating nickel
nanoparticles in a natural rubber matrix for various loadings of the filler. Structural, morphological, magnetic
and mechanical properties of the compositeswere evaluated along with a detailed study of dielectric
properties. Itwas found that nickel particleswere uniformly distributed in the matrix without agglomeration
resulting in a magnetic nanocomposite. The elastic properties showed an improvement with increase
in filler content but breaking stress and breaking strain were found to decrease. Dielectric permittivity
was found to decrease with increase in frequency, and found to increase with increase in nickel loading.
The decrease in permittivity with temperature is attributed to the high volume expansivity of rubber at
elevated temperatures. Dielectric loss of blank rubber as well as the composites was found to increase
with temperature.
Stable, OH free zinc oxide (ZnO) nanoparticles were synthesized by hydrothermal method by varying the
growth temperature and concentration of the precursors. The formation of ZnO nanoparticles were confirmed by x-ray
diffraction (XRD), transmission electron microscopy (TEM) and selected area electron diffraction (SAED) studies. The
average particle size have been found to be about 7-24 nm and the compositional analysis is done with inductively
coupled plasma atomic emission spectroscopy (ICP-AES). Diffuse reflectance spectroscopy (DRS) results shows that the
band gap of ZnO nanoparticles is blue shifted with decrease in particle size. Photoluminescence properties of ZnO
nanoparticles at room temperature were studied and the green photoluminescent emission from ZnO nanoparticles can
originate from the oxygen vacancy or ZnO interstitial related defects.
Binu, Varghese; Dr. Prathapachandra Kurup, M R(Cochin University of Science & Technology, February , 2009)
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The thesis is an introduction to our attempts to evaluate
the coordination behaviour of a few compounds of our interest.
Semicarbazones and their metal complexes have been an active area of
research during the past years because of the beneficial biological activities
of these substances. Tridentate NNO semicarbazone systems formed from
heterocyclic and aromatic carbonyl compounds and their transition metal
complexes are well-authenticated compounds in this field and their
synthesis and characterization are well desirable. Hence, we decided to
develop a research program aimed at the synthesis and characterization of
novel semicarbazones derived from 2-benzoylpyridine and 2-acetylpyridine
and their transition metal complexes. In addition to various physicochemical
methods of analysis, single crystal X—Ray diffraction studies were
also used for the characterization of the complexes.
Description:
Department of Applied Chemistry,
Cochin University of Science and Technology
Sreeja,P B; Prathapachandra Kurup,M R(Department of Applied Chemistry,Faculty of Science, 2004)
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This study concentrates the chemical properties of hydrazones due to its chelating capability and their pharmacological applications. Studies cover the preparation of different acid hydrazones and their structural studies and studies on their antimicrobial activity, synthesis and spectral characterization of different complexes of copper oxovanadium, manganese, nickel etc. Effect of incorporation of heterocyclic bases to the coordination sphere, change in the biological activity of acid hydrazones upon coordination, development of X-ray quality single crystals and its X-ray diffraction studies, studies on the redox behavior of the coordinated metal ions and correlation between the stereochemistry and biological activities.