Sugunan, S; Bindhu, J; Disha; Jessey, V(Indian Journal of Chemistry, July , 1997)
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Abstract:
The Lewis acidity of yttrium and dysprosium exchanged
zeolite Y and ZSM-5 has been determined by titration method
using Hammett indicators. The acidity of the Y form increases
with increase in concentration of the rare earth cation in the Y
zeolite. It is independent of the amount of the rare earth ion for
ZSM-5. The data have been correlated with the activity of these
zeolites for the esterification of butanol using acetic acid.
The present work undertakes the preparation and physico-chemical characterisation of iron promoted sulphated zirconia
(SZ) with different amounts of iron loading and their application to Friedel-Crafts benzoylation of benzene, toluene and xylene
under different experimental conditions, XRD and laser Raman techniques reveal the stabilisation of the tetragonal phase of
zirconia and the existence of iron in highly dispersed form as Fe203 on the catalyst surface. The surface acidic properties were
determined by ammonia temperature programmed desorption (TPD) and perylene adsorption, The results were supported by
the TGA studies after adsorption of pyridine and 2,6-dimethylpyridine (2,6-DMP), Strong Lewis acid sites on the surface, which
are evident from TPD and perylene adsorption studies. explain the high catalytic activity of the systems towards benzoylation.
The experimental results provide evidence for the truly heterogeneous nature of the reaction. The studies also establish the
resistance to deactivation in the metal incorporated sulphated systems.
Manju, Kurian; Sugunan, S(Indian Journal of Chemistry, October , 2003)
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Abstract:
Iron, aluminium and mixed iron aluminium pillared clays have been prepared by partial hydrolysis method and doped
with IO% Mo, V and Cr. The samples have been characterised by XRD, FTIR and surface area and pore Volume
measurements. The surface acid site distribution has been determined by temperature programmed desorption of ammonia.
Vanadia incorporated systems show maximum acidity. Benzylation of o-xylene has been done as probe reaction to test
catalytic activity. Benzyl chloride is a superior benzylating agent compared to benzyl alcohol in activity and selectivity.
Cent percent selectivity towards monobenzylated product is obtained in all the cases. Fe pillared systems exhibit maximum
activity. The catalytic activities of the systems can be correlated with the amount of strong add sites. The effects of various
reaction variables on the reaction have been studied. Presence of moisture has a diminishing effect on the reaction rate.
Sugunan, S; Nishamol, K(Indian Journal of Chemistry, May , 2002)
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Abstract:
The liquid-phase Friedel-Crafts acylation of toluene using benzoyl chloride as benzoylating agent has heen carried out over Nix, Mn(l-x)Fe2 O4 (x=O, 0.2, 0.4, 0.6, 0.8 and 1.0) type systems under different reaction conditions. It is observed that the systems with high 'x' values are effective for the conversion of BOC and the selective formation of 4-MBP. Selectivity for 4-MBP over MnFe2O4 is more than 90% under the optimized reaction conditions. Sites of moderate acidity is effective in calalyzing the benzoylation reaction.
Anantaraman, R; Sugunan, S(Indian Journal of Chemistry, August , 1982)
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Abstract:
Kinetics of mercuric chloride catalysed solvolysis of benzyl chloride have been studied in water. 10% aq. ethanol, 10,20 and
30% aq. acetone and 20% aq. DMSO. The results confirm the operation of a mass law effect.
Sugunan, S; Renuka, N K(Indian Journal of Chemistry, June , 2002)
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Abstract:
A series of supported vanadia systems have been prepared by
excess solvent technique using La203 and DY203 as supports.
Physical characterization has been carried out using XRD, FTIR,
TG studies, BET surface area measurement, pore volume analysis
etc. Cyclohexanol decomposition has been used as a test reaction
for evaluating the acid base properties of the supported system.
The oxidative dehydrogenation of ethylbenzene has been
employed as a chemical probe reaction to examine the catalytic
activity. The active species correspond to amorphous and
crystalline tetrahedral vanadyl units in the supported system.
Sankara Raman, S; Nampoori, V P N; Vallabhan, C P G; Ambadas, G; Sugunan, S(American Institute of Physics, 1995)
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Abstract:
The thermal diffusivity of y-alumina is determined by the photoacoustic method. The method is
calibrated by determining the thermal diffusivity of copper and aluminum. The effect of the
chemisorbed hydroxyl groups or thermal diffusivity is studied by degassing the sample at different
temperatures.
The heterogeneous photocatalytic degradation of methylorange over TiO2 is studied
and is found to be cost effective. Effect of Zirconium metal incorporation over titania system is investigated. Photocatalytic degradation of methylorange using solar radiation is
found to be highly economical when compared with the processes using artificial UV
radiation, which require substantial electrical power input. The characterization of titania as
well as modified zirconium metal doped titania systems are done using XRD, FTIR and
EDAX measurements. The catalytic activities of different systems are also compared and is
tried to correlate with the crystallite size and presence of dopant metal.
Shali, N B; Sugunan, S(Springer Netherlands, 2007)
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Abstract:
Lanthana modified sol-gel titania is prepared
through particulate sol-gel route and the physico-chemical
characterizations of the prepared systems were done using
X-Ray diffration, EDX, BET surface area-pore volume measurements
and TG-DTG analysis. Benzophenone was observed
to be the sole product in the TiO2 photocatalyzed
oxidation of benzhydrol in oxygen purged acetonitrile. The
influence of various parameters, like irradiation time, amount
of catalyst, concentration of the catalyst and other factors on
the photocatalytic oxidation has been investigated. The proposed
mechanism envisages the involvement of a superoxide
radical anion.
Sugunan, S; Binitha, N N(Journal of Applied Polymer Science,Wiley InterScience, March 16, 2007)
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Abstract:
In situ polymerization of aniline is done
inside the pillared clay matrix. The nonswellable pillared
clay confined matrix allows efficient polymerization that
leads to nanofibrous morphology. As a result high polymer
order and crystallinity is attained and is evident from
XRD patterns. The strong interaction between the clay
layers and polyaniline (PANI) is understood from FTIR and DRS spectra. Additionally these analytical results suggest that the prepared PANI is in the doped state. The
PANI/pillared clay nanocomposite formation gives additional
thermal stability to the polymer backbone and is clear from the DTG curves.
Transition metal-loaded (3%) nanocrystalline sulfated titania (ST) powders are prepared using the sol–gel technique. Anatase is found as the active phase in all the samples. Sulfate ion impregnation decreases the crystallite size and stabilizes the anatase phase of TiO2. Acidity of the samples is found to increase by the incorporation of sulfate ion and also by the modification by transition metal ions. All the prepared catalysts are found stable up to 700 °C.
Sugunan, S; Bindhu, Jacob; Binoy,Jose(Indian Journal of Chemistry, October , 1999)
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Abstract:
The results of a detailed study of the propionylation of anisole over various medium and large pore zeolites such as H-ZSM-5, H-beta, H-Na-beta. H-mordenite. H-Y and H-RE- Y are presented and discussed. In addition, homogenous catalysts and amorphous Si02-Al2O3 are also included for comparison, The catalyst and process parameters are optimised to enhance the conversion of propionyl chloride(PC) and selectivity to 4-methoxypropiophenone(4-MOPP).
Sugunan, S; Benny, Thomas(Indian Journal of Chemistry, February , 1995)
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Abstract:
The Setschenow parameter and thermodynamic
parameters of transfer of 2- and 4- hydroxybenzoic acids
from water to salt solutions have been reported. The data
have been rationalised by considering the structure
breaking effects of the ions of the salts, the localized
hydrolysis model, the internal pressure theory and the
theory of water structure due to Symons.
The Setschenow parameter and thermodynamic parameters of transfer of 2-, 3-, and 4-methylbenzoic acids
from water to salt solutions have been reported. The data have been rationalized by considering the structure breaking
effects of the ions of the salts, the localized hydrolysis model, and the internal pressure theory.
Sugunan, S; Benny, Thomas(Journal of Solution Chemistry, 1994)
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Abstract:
The Setschenow parameter and thermodynamic parameters of transfer of
2-, 3- and 4-fluorobenzoic acid from water to salt solution are reported.
The data have been rationalized by considering the structure breaking effects of the ions of the salts, the localized hydrolysis model and the internal
pressure theory.
Sugunan, S; Anantaraman, R(Indian Journal of Chemistry, December , 1982)
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Abstract:
Kinetics of mercuric chloride catalysed solvolysis of l-butyl
chloride, benzyl chloride. p-methylbenzyl chloride, l-phenylethyl
chloride and triethylcarbinyl chloride have been studied in aq.
DMSO, aq. acetonitrile and aq. ethanol. The kinetic data fit a second
order rate equation in aq. DMSO. The calculated values of the
second order rate coefficients increase in the case of aq. acetonitrile
and aq. ethanol. The order in catalyst in 95%(v/v) aq. DMSO is less
than unity.
Nishamol, K; Rahna, K S; Sugunan, S(Elsevier, 2004)
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Abstract:
Various compositions of chromium manganese ferrospinels were tested as catalysts for the vapour phase alkylation of aniline with methanol. The samples were prepared by room temperature co-precipitation technique and characterized by various physico-chemical methods. The acidity–basicity determination revealed that the samples possess greater amount of basic sites than acidic sites. All the ferrite samples proved to be selective and active for N-monoalkylation of aniline leading to N-methyl aniline; Cr0.6Mn0.4Fe2O4, Cr0.8Mn0.2Fe2O4 and CrFe2O4 exhibited cent percent selectivity for N-methyl aniline. Neither C-alkylated products nor any other side products were detected for all catalyst samples. The catalytic activity of the samples studied in this reaction is related to their acid–base properties and also on the cation distribution. Under the optimized reaction conditions all the systems showed constant activity for a long duration.
Iron and mixed iron aluminium pillared montmorillonites prepared by partial hydrolysis method was subjected to room temperature exchange with transition metals of the first series. The materials exhibit good structural as well as thermal stability. Exchanged metals were found to be present inside the porous network, in the environs of the pillars. Mixed pillaring resulted in the intercalation of Al 13 like polymers in which Al is partially substituted by Fe. The acidic structure was followed by temperature programmed desorption of ammonia and cumene cracking test reaction. Weak and medium sites overshadow the strong sites in all systems. However, exchange with metals increases the number of strong sites. The prepared materials are efficient catalysts for gas phase MTBE synthesis. The catalytic activity can be well correlated with the total amount of weak and medium acid sites.
Sreekumar, K; Raja, T; Kiran, B P; Sugunan, S; Rao, B S(Elsevier, 1999)
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Abstract:
The reaction of aniline with methanol was carried out over Zn1-xNixFe2O4 (x= 0, 0.2, 0.5, 0.8 and 1) type systems in a
fixed-bed down-flow reactor. It was observed that systems possessing low ``x'' values are highly selective and active for mono
N-alkylation of aniline leading to N-methyl aniline. Selectivity for N-methyl aniline over ZnFe2O4 was more than 99% under
the optimized reaction conditions. Even at methanol to aniline molar ratio of 2, the yield of N-methyl aniline was nearly
55.5%, whereas its yield exceeded 67% at the molar ratio of 7. The Lewis acid sites of the catalysts are mainly responsible for
the good catalytic performance. Cation distribution in the spinel lattice influences their acido-basic properties, and hence,
these factors have been considered as helpful to evaluate the activity and stability of the systems.
Sreekumar, K; Jyothi, T M; Talawar, M B; Kiran, B P; Rao, B S(Elsevier, 2000)
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Abstract:
A series of ferrites having the general formula Zn1-xCoxFe2O4 (x=0, 0.2, 0.5, 0.8 and 1.0)were prepared by soft
chemical route. The materials were characterized by adopting various physico-chemical methods. The reaction of aniline
with methanol was studied in a fixed-bed reactor system as a potential source for the production of various methyl anilines.
It was observed that systems possessing low ‘ x’ values are highly selective and active for N-monoalkylation of aniline
leading to N-methylaniline. Reaction parameters were properly varied to optimize the reaction conditions for obtaining
N-methylaniline selectively and in better yield. Among the systems Zn0.8Co0.2Fe2O4 is remarkable due to its very high
activity and excellent stability. Under the optimized conditions N-methylaniline selectivity exceeded 98%. Even at a
methanol to aniline molar ratio of 2, the yield of N-methylaniline was nearly 50%, whereas its yield exceeded 71% at the
molar ratio of 5. ZnFe2O4, though executed better conversion than Zn0.8Co0.2Fe2O4 in the initial period of the run,
deactivates quickly as the reaction proceeds. The Lewis acidity of the catalysts is mainly responsible for the good
performance. Cation distribution in the spinel lattice influences their acido-basic properties and, hence, these factors have
been considered as helpful parameters to evaluate the activity of the systems.