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    Adsorption of fluoride from aqueous solution by alumina of alkoxide nature: Batch and continuous operation

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    In this investigation, we report the adsorption potential of alkoxide origin alumina for defluoridation of drinking water using batch and continuous mode of operations. The effects of different operating parameters such as adsorbent dose, initial fluoride concentration, pH of the solution and interfering ions (usually present in groundwater) were studied with a view to understand the adsorption behavior of the material under various conditions. A thermodynamic study shows that the adsorption of fluoride by alkoxide origin alumina is an exothermic and spontaneous process. The kinetic results showed that the fluoride sorption follows pseudo-second-order kinetics. The applicability of adsorbent in the field is also tested through column breakthrough studies. It has been observed that with an increase in the flow rate and initial fluoride concentration, the breakthrough curve becomes sharper and the breakthrough time and adsorbed fluoride ion concentration decrease. The breakthrough curve also becomes steeper as the bed height increases. The alkoxide origin alumina based adsorbent media can be used directly for field applications since it is also commercially available in granular form

    Pure phase LaFeO3 perovskite with improved surface area synthesized using different routes and its characterization

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    Three different wet chemistry routes, namely co-precipitation, combustion and sol–gel methods were used to synthesize LaFeO3 perovskite with improved surface area. The synthesized perovskite was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectrometer (EDS), Brunauer–Emmett–Teller (BET) nitrogen adsorption, ultraviolet diffused reflectance spectroscopy (UVDRS) and Fourier transform infrared (FTIR) spectroscopy techniques. Improved surface area was observed for all three methods as compared to the previously reported values. The perovskite synthesized using sol–gel method yields comparatively pure, crystalline phase of LaFeO3 and relatively higher surface area of 16.5 m2 g−1 and porosity. The material synthesized using co-precipitation method yielded other phases in addition to the targeted phase. The morphology of perovskite synthesized using co-precipitation method was uniform agglomerates. Combustion method yields flakes type morphology and that of sol–gel method was open pore type morphology. The selection of method for perovskite synthesis largely depends on the targeted application and the desired properties of perovskites. The results reported in this study are useful for establishing a simple scalable method for preparation of high surface area LaFeO3 as compared to solid-oxide method. Further, the typical heating cycle followed for calcinations resulted in relatively high surface area in the case of all three methods

    Antigenotoxic potential of Gymnema montanum leaves on DNA damage in human peripheral blood lymphocytes and HL-60 cell line

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    In this study we have evaluated the genoprotective effect of the ethanol extract of Gymnema montanum (GLEt) leaves in human peripheral blood lymphocytes and HL-60 cell line in vitro using the comet assay. DNA damage was induced by treating the cells with H2O2 and methyl methane sulphonate (MMS). GLEt treatment effectively protected the lymphocytes and HL-60 cell line from H2O2-induced oxidative DNA damage in a dosedependent manner whereas it was not effective against alkylative DNA damage caused by MMS. The global percent repair efficiency also showed that both pre- and post- GLEt treatment provided effective protection against H2O2 induced DNA damage but not as effective against MMS. At 200 lg ml21 level, its repair capacity against H2O2 induced DNA damage was comparable to that of vitamin-C (100 lM). Furthermore, exposure to GLEt reduced the formation of apoptotic cells caused by H2O2, which was demonstrated by the decreased sub-G1-DNA content in cell cycle analysis and apoptotic frequencies of lymphocytes in an annexin-V binding assay. In addition, GLEt was found to have effective peroxide scavenging ability in dose-dependent manner. The protective efficiency of the extract was found to be directly proportional to its total phenolic content. The present study indicates that G. montanum leaves are a significant source of phytochemicals with antigenotoxic and antioxidant activity, and thus has potential therapeutic use. Environ. Mol. Mutage

    Assessment of heavy metal content in suspended particulate matter of coastal industrial town, Mithapur, Gujarat, India

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    Heavy metal concentrations in suspended particulate matter (SPM) were investigated for their distribution and source in the atmosphere of coastal industrial town, Mithapur, Gujarat, India. SPM, at 10 locations covering three seasons, were trapped on glass fibre filters using high volume samplers and quantification of metals (Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn) was done using Atomic Absorption Spectrometry employing HNO3 based wet digestion. Results show relatively low concentrations of SPM (211.3 to 375.2 μg/m3) compared to National Ambient Air Quality Standard (NAAQS), specified By Central Pollution Control Board (CPCB, India), however, they were 2–3 times higher as compared to reference site. Among the heavy metals Cr, Mn and Pb levels were low, while Ni and Cd found to be exceeding the USEPA standards. The metal levels were also compared with those reported for other rural, coastal, industrial and urban parts around the world. Enrichment Factor analysis indicated that Cd, Zn, Cu, Pb and Ni were highly enriched relative to their crustal ratios (to Fe) and correspond to substantial contribution of anthropogenic source of these metals. The source identification was carried out by principal component analysis by applying a Varimax Rotated Component Matrix

    Influence of zeolitic structure on photoreduction property and hydrogen evolution reaction

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    A new photocatalytic material developed by supporting TiO2 in combination with transition metal ion like cobalt and heteropolyacid (HPA) on the surface is facilitating enhanced photoreduction of water and methyl orange. Zeolites being a solid acid play an important role in the electron transfer reaction, facilitated by the Lewis acid sites in the form of aluminium ions. In the present work, four different zeolite matrices namely, NaY zeolite, ultrastable zeolite Y, beta zeolite and titanium silicate-1 have been used for the synthesis of new photocatalytic materials. These materials have been evaluated for water splitting by an initial screening procedure using methyl orange photoreduction. The photocatalyst containing Na Y has emerged as a potential photocatalyst with hydrogen evolution rate of 2730 mmol/h/g of TiO2. Hydrogen evolution was not observed for the composite photocatalysts synthesized using the other zeolite matrices. It has been observed that physicochemical properties like Si/Al ratio, acidity and basicity of the zeolite support have a tremendous influence on the photoreduction property of these zeolite matrices

    Hydrogen evolution by a low cost photocatalyst: Bauxite residue

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    Bauxite residue or red mud which is an aluminium industry waste has been used as a novel low cost photocatalyst active in visible light for the generation of hydrogen from water. The driving force behind the use of bauxite residue as a photocatalyst is not only the fact that it is widely available but also bauxite residue is a fine grained mixture of oxides and hydroxides (Fe2O3, TiO2, SiO2, and Al2O3, Al(OH)3). The photocatalyst was characterized with respect to BET-SA, UV-DRS, XRD, SEM and EDX. Hydrogen yield of 4600 mmol/h/g of TiO2 was achieved as compared to hydrogen evolution rate of 164 mmol/h/g of TiO2 for commercially available titania Degussa P-25. However, the hydrogen evolution was 20.85 mmol/h/g of photocatalyst. The results suggest that bauxite residue appears to be a novel low cost photocatalyst. The various operating conditions of photocatalytic hydrogen generation were studied which include amount of catalyst, illumination intensity, illumination time, effect of various sacrificial donors etc

    Chitosan based mesoporous Ti–Al binary metal oxide supported beads for defluoridation of water

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    In the present study, the performance of Ti–Al binary metal oxide supported beads using chitosan template was studied for fluoride removal from drinking water. The adsorbent was synthesized by precipitation method and characterized using FTIR, SEM, XRD and BET. The higher surface area of the synthesized adsorbent 323.83m2/g results in a much higher fluoride removal capacity Qmax = 2.22mgg−1 as compared to bare chitosan. Pore size of beads is 42.97 Å, suggesting mesoporous nature of adsorbent. Material works very effectively at all pH except at pH greater than 9. The presence of carbonate and bicarbonate ions showed significant decline in the fluoride removal capacity of adsorbent. The experimental data fitted well to Langmuir adsorption model. The kinetic studies indicate that the system follows the pseudo-second-order and intra-particle diffusion model. Thermodynamic study reveals that the fluoride adsorption by Ti–Al binary metal oxide supported beads is an exothermic and spontaneous process. Alum appears to be the promising regeneration media showing 80% regeneration. The applicability of the adsorbent for fluoride removal was tested in field water collected from the Dhar district in Madhaya Pradesh, India

    Efficient hydrogen supply through catalytic dehydrogenation of methylcyclohexane over Pt/metal oxide catalystsEfficient hydrogen supply through catalytic dehydrogenation of methylcyclohexane over Pt/metal oxide catalysts

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    This paper describes the results of experiments on dehydrogenation of methylcyclohexane over Pt supported on metal oxides (Pt/MO) and Pt supported on perovskite (Pt/Per) catalysts. The reaction is being considered as a means for delivery of hydrogen to fueling stations in the form of more easily transportable methylcyclohexane. Among Pt/MO catalysts, the best activity as determined by the hydrogen evolution rate was observed over Pt/La2O3 catalyst at 21.1 mmol/gmet/min. Perovskite-supported catalysts exhibited relatively higher activity and selectivity, with Pt/La0.7Y0.3NiO3 giving the best performance. This Pt/Per catalyst had an activity of ca 45 mmol/gmet/min with nearly 100% selectivity towards dehydrogenation. The catalysts were characterized using XRD, CO-chemisorption and SEM-EDXA techniques. The present study reports catalysts that minimize the use of Pt and explores tailoring the properties of the perovskite structure

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