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KM Parida

Publications and source records attributed to KM Parida.

8 recordsLinked to original sources

Studies on Anion Promoted Titania.1: Preparation, Characterization, and Catalytic Activity toward Alcohol and Cumene Conversion Reactions of Phosphated Titania.

Phosphate impregnated titania samples with varying amount of phosphate have been prepared by solid-solid kneading as well as aqueous impregnation method. All the samples are characterized by XRD, TG-DTA, and N(2) adsorption-desorption isotherm. Surface area is found to increase with the increase in phosphate content up to 7.5 wt% loading and thereafter decreases. The average pore diameter and crystallite size of titania decreases with the addition of phosphate. However, total acidity (determined by base adsorption method) and the catalytic activity increases with the increase in phosphate content up to 10 wt%. Phosphated samples prepared using phosphoric acid as the source of phosphate exhibit higher acidity compared to the samples prepared using (NH(4))(3)PO(4). However, the sample prepared from (NH(4))(3)PO(4) shows the presence of both acid and basic sites. Though from the cumene conversion study it is understood that phosphated samples contain both Lewis and Brønsted acid sites, the latter predominates over the former. Copyright 1999 Academic Press.

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SO2-4/TiO2-SiO2 Mixed Oxide Catalyst, I: Synthesis, Characterization, and Acidic Properties.

A series of sulfate-doped titania-silica mixed oxides have been prepared by immersing titania-silica gel in the required volume of sulfuric acid, followed by drying. The mixed oxide gel is obtained by hydrolyzing an equimolar mixture of tetraethylorthosilicate (TEOS) and tetrabutylorthotitanate (TBOT) at pH 3. The materials, after calcining at 723 K for 4 h, are characterized by XRD, FT-IR, the BET method, and surface acid strength by the Hammett indicator method. The catalytic activity tests are carried in a fixed bed catalytic reactor (i.d. = 10 mm) for alcohol conversion, whereas cumene cracking/dehydrogenation reactions are carried out in a micropulse reactor. XRD results shows that the titania-silica mixture is amorphous and the crystallization starts with sulfation. The surface of the mixed oxide contains both bridged and normal hydroxyl groups, as observed from FT-IR data. The surface area of the material is not much altered by sulfation and lies within 50 m2/g. The acid strength of 4 wt% SO2-4/TiO2-SiO2 is found to be stronger than that of 100% concentrated H2SO4. In the case of 2-propanol conversion, low acetone selectivity indicates the presence of weak basic sites, whereas methanol conversion over all solids shows that dehydration follows a parallel and consecutive pathway. A good correlation is found between the cumene cracking and the acidity of the catalysts. Copyright 1999 Academic Press.

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Studies on Indian Ocean Manganese Nodules.

The effects of alkali (sodium hydroxide) treatment on the physico-chemical properties and catalytic activity for H2O2 decomposition and CO oxidation of Indian Ocean manganese nodules have been studied. The surface area, surface oxygen, surface hydroxyl groups, etc. increase with alkali treatment up to 0.05 M and there after show a decreasing trend. The high catalytic activity of 0.05 M NaOH treated samples are correlated with the surface properties. Copyright 1999 Academic Press.

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Studies on Indian Ocean Manganese Nodules

The oxidation of thiols to corresponding disulfides by Indian Ocean ferromanganese nodules has been studied under varying experimental conditions. More than 90% conversion of thiols (2.5 x 10(-3) mol) was achieved at 35&deg;C using 0.1 g nodules. The oxides of Mn, Fe, Ca, Mg, and Al and surface oxygen in the nodules are most likely responsible for the oxidation of thiols. Under identical conditions the oxidative conversion of thiols decreases in the order 1-dodecanethiol < 1-hexanethiol < 1,4-butanedithiol < alpha-toluenethiol. Copyright 1998 Academic Press. Copyright 1998Academic Press

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Studies on Indian Ocean Manganese Nodules

A series of strontium-lanthanum oxide mixed manganese nodules were prepared and characterized by X-ray diffraction, nitrogen adsorption-desorption, electrical conductivity, and surface excess oxygen. X-ray diffraction patterns confirm the formation of perovskite-type oxides at low strontium content (x </= 0.5, in La1-xSrxMO3, where M denotes the transition metal present in nodules), whereas at 0.6 </= x </= 0.8, La2O3 and SrO are detected in addition to the perovskite-type oxides. The catalytic activities for hydrogen peroxide decomposition and carbon monoxide oxidation increase with an increase in Sr substitution for La, attain a maximum at x = 0.4, and then decrease with further increase in Sr. The activities have been correlated with various physicochemical properties.

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Studies on Indian Ocean Manganese Nodules

Adsorption of aqueous selenite (SeO32-) on Indian Ocean manganese nodules was studied as a function of time, temperature, pH, and concentrations of adsorbate and adsorbent in acetic acid-sodium acetate buffer medium. Analysis of adsorption data supports a heterogeneous nature for the surface of manganese nodules. The adsorption capacity of various manganese nodules for selenite was correlated with their chemical composition and surface properties.

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Studies on Ferric Oxide Hydroxides

Adsorption of selenite (SeO2-3) on different polymorphic forms of iron oxyhydroxides and amorphous ferrihydrite was studied as a function of time, temperature, pH, and concentration of adsorbate(s) and adsorbent(s). Analysis of adsorption data indicates that the surfaces of all the forms of oxyhydroxides and ferrihydrite are heterogeneous in nature and that adsorption fits into a heterogeneous site binding model. The adsorption capacity of oxyhydroxides for SeO2-3 follows the order beta-FeOOH < alpha-FeOOH < gamma-FeOOH < delta-FeOOH < ferrihydrite.

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Studies on Indian Ocean Manganese Nodules

A series of rare earth oxide mixed manganese nodules (perovskite type mixed oxides) have been prepared by coprecipitation method followed by calcination at 900&deg;C and characterized by different techniques. The effect of rare earth ions on the surface, textural and catalytic activity for the oxidation of CO, and decomposition of H2O2 have been discussed. The activity for CO oxidation followed an order: Pr >/= La > Nd > Yb > Dy > Tb > Sm > Tm > Gd > Eu > Ce.

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