Oxidation of Toluene on Supported and Unsupported LaCoO3 Perovskites Catalyst

2021 ◽  
pp. 282-284
Author(s):  
H.S. Goswami ◽  
Shveta Acharya
Keyword(s):  
Surface Area ◽  
Surface Acidity ◽  
Specific Area ◽  
Vapour Phase ◽  
Maximum Activity ◽  
Heterogenous Catalysis ◽  
Heterogeneous Catalytic ◽  
Surface Basicity ◽  
Density Surface

Perovskite type oxide are known to be catalysts for a number of reactions such as total and partial oxidation, hydrocracking, hydrogeneous, hydrogenolysis and reduction etc. Efforts has largely been directed towards synthesis of unsupported and supported perovskites oxides of moderates or high specific area, their bulk and surface properties and their role in heterogenous catalysis. Oxidation of aromatic and aliphatic hydrocarbon over LaMO3 (M=Al, Ni, Mn, Co, Fe, Cr etc.) perovskites have been studied. Vapour phase catalytic oxidation of toluene over perovskites Viz., LaCoO3, LaCoO3/ SiO2 and LaCoO3/Al2O3 has been studied. The characterization of the catalyst was carried out using technique Viz. I.R., Surface area, Packing density. Surface acidity, Surface basicity. The surface area measurements in the temperature range 350ºC to 600ºC. The maximum surface area & maximum activity was observed at 450ºC. The heterogeneous catalytic vapour phase oxidation of toluene give benzaldehyde, benzoic acid, maleic acid and CO2 as products over LaCoO3 and LaCoO3 supported on Al2O3 and SiO2 as catalyst. The LaCoO3 supported on Al2O3 has been found to be the most active and selective catalyst giving 84.0% selectivity for benzaldehyde at 450⁰C with surface area 78.9m2/g. The overall Kinetic analysis indicate that the oxidation of Toluene to benzaldehyde is first order. The order of catalytic reactivity is LaCoO3/Al2O3 > LaCoO3/ SiO2 > LaCoO3.

scholarly journals The Characterization of Heterogeneous Nanocatalyst of Biohydroxyapatite-Lithium and its Application for Converting Malapari Seed Oil (Milletia pinnata L.) to Biodiesel

2018 ◽  
Vol 34 (4) ◽  
pp. 1817-1823
Author(s):  
I. Nengah Simpen ◽  
I. Made Sutha Negara ◽  
Ni Made Puspawati
Keyword(s):  
Particle Size ◽  
Surface Area ◽  
Seed Oil ◽  
Surface Acidity ◽  
Average Particle Size ◽  
Bet Surface Area ◽  
Average Particle ◽  
Bovine Bone ◽  
Heterogeneous Nanocatalyst ◽  
Surface Basicity

Heterogeneous nanocatalyst of biohydroxyapatite-lithium (HA-Li) has been prepared through modification of HA extracted from bovine bone waste with Li at various calcination temperatures (400-700oC). Characterizations of the heterogeneous catalysts were including surface acidity-basicity, functional groups, BET surface area, particle size, and surface morphology. Optimization of catalyst ratios (1-7%) with the best characterization was applied for converting Malapari seed oil (Milletia pinnata L.) to biodiesel. The characterization results showed that HA-Li catalyst calcinated at 600oChad the highest surface basicity and Lewis acid sites revealing specific functional group of O-Li at wavenumber of 1612.49 cm-1. BET surface area of HA-Li catalyst decreased with increased average particle size. SEM analysis suggested that morfology of catalysts formed stack of agglomerates. The highest yield of biodiesel obtained on a catalyst ratio of 5% was 88.16%. GC-MS analysis showed 10 peaks, and 5 of the peaks exhibiting the highest percentage area were identified as methyl oleic, methyl palmitic, methyl erusic, methyl stearic, and methyl linoleic.

Characterization of pore morphology in molecular crystal explosives by focused ion-beam nanotomography

2010 ◽  
Vol 25 (7) ◽  
pp. 1362-1370 ◽  
Author(s):  
Ryan R. Wixom ◽  
Alexander S. Tappan ◽  
Aaron L. Brundage ◽  
Robert Knepper ◽  
M. Barry Ritchey ◽  
...  
Keyword(s):  
Surface Area ◽  
Molecular Crystal ◽  
Focused Ion Beam ◽  
Ion Beam ◽  
Three Dimensional ◽  
Polymer Materials ◽  
Detonation Properties ◽  
Indirect Measure ◽  
Density Surface

The initiation and detonation properties of explosives are often empirically correlated to density, surface area, and particle size. Although these correlations are sometimes used successfully to predict the performance of bulk samples, the data are spatially averaged, which unfortunately muddles information critical to understanding fundamental processes. Density and surface area are essentially an indirect measure of porosity, which is arguably a more appropriate metric in many applications. We report the direct characterization of porosity in polycrystalline molecular crystal explosives by focused ion beam nanotomography, a technique that is typically reserved for robust materials such as ceramics and metals. The resulting three-dimensional microstructural data are incredibly rich, promising a substantial advance in our ability to unravel the processes governing initiation and detonation of molecular crystal explosives. In a larger context, this work demonstrates that focused ion beam nanotomography may be successfully extended to the investigation of nanoscale porosity in other molecular crystal or polymer materials.

scholarly journals KARAKTERISASI KATALIS BATU PADAS LEDGESTONE TERAKTIVASI ASAM DAN APLIKASINYA PADA PEMBUATAN BIODIESEL DARI MINYAK JELANTAH

Jurnal Kimia ◽  
2016 ◽  
Author(s):  
Ika Juliana ◽  
Ida Ayu Gede Widihati ◽  
Oka Ratnayani
Keyword(s):  
Cation Exchange ◽  
Surface Area ◽  
Cation Exchange Capacity ◽  
Active Sites ◽  
Surface Acidity ◽  
Acid Value ◽  
Exchange Capacity ◽  
Gas Chromatography Mass Spectrometry ◽  
Acid Activation

This research aims to improve characteristics of ledgestone catalyst by using acid activation with various concentrations. The acid used for activation was H2SO4 with concentrations of 1, 2 and 3M. The characterization of catalysts was carried out by acid-base titration method to determine the surface acidity, methylene blue adsorption to measure the spesific surface area of ??the catalyst, and the NH4OAc extraction method to measure the value of cation exchange capacity of the catalyst. Ledgestone catalyst with the best character was applied to convert waste cooking oil into biodiesel. The characterization of biodiesel was carried out by densitometry to determine the density of biodiesel, Oswald viskosimetry to measure the viscosity, and Gas Chromatography-Mass Spectrometry (GCMS) to determine the composition of chemical compounds of the biodiesel. The results showed that the concentration of acid used to activate ledgestone catalyst with the best character was 1M. This acid-activated ledgestone (catalyst A1) had a value of surface acidity, surface area, active sites number, and high cation exchange capacity were 0.3530 ± 0.0011 mmol / gram and35.7581 m2/gram, 2.1258 x 1020 atoms/gram, and 5.88 me/100 g, respectively. The concentration of catalyst A1 producing the highest biodiesel yield was 1% w/v. The produced biodiesel was 74,71% with 0.02% FFA, acid value of 0.0438 mg KOH/gram biodiesel, density of 0.7850 g/mL, kinematic viscosity of 0.4650 cSt. Two major compounds of the biodiesel were methyl hexadecanoate with area of 71.84% and cis methyl-9-octadecenoate with area of 28.16%.

scholarly journals Oxidation of 3- and 4-Methylpyridines on Vanadium-Anatase and Vanadium-Rutile Catalysts

2012 ◽  
Vol 14 (4) ◽  
pp. 337
Author(s):  
O.K. Yugay ◽  
T.P. Mikhailovskaya ◽  
D.Kh. Sembaev ◽  
P.B. Vorobyev
Keyword(s):  
Surface Area ◽  
Isonicotinic Acid ◽  
Thermal Dissociation ◽  
Dissociation Rate ◽  
Bet Surface Area ◽  
Titanium Catalysts ◽  
Heterogeneous Catalytic ◽  
Vanadium Titanium ◽  
Crystal Modifications

<p>Heterogeneous catalytic vapor-phase oxidation of methylpyridines is “green”, the most simple and perspective method for obtaining pyridinecarboxylic acids. Vanadium-titanium catalysts have a wide application in some important industrial processes of oxidation. Oxidation of 3-and 4-methylpyridine on vanadium-titanium catalysts has been investigated and for its preparation various titanium crystal modifications were used. Characterization of the catalysts was carried out by using the X-ray diffraction, N<sub>2</sub>-adsorbtion and thermal dissociation of V<sub>2</sub>O<sub>5</sub>. It was found that the use of anatase type of TiO<sub>2</sub> with a higher BET surface area enhances the activity of the vanadium-titanium catalyst extremely. XRD-characterization of catalysts demonstrated that the only V<sub>2</sub>O<sub>5</sub> and anatase or V<sub>2</sub>O<sub>5</sub> and rutile phase was detected. It was established that the use of titanium dioxide of crystal modifications of anatase increases on the order of the dissociation rate V<sub>2</sub>O<sub>5</sub>. It was shown that vanadium-titanium catalysts’ activity and selectivity in investigated processes depends on TiO<sub>2</sub> crystal modifications.V<sub>2</sub>O<sub>5</sub>-anatase is more active and selective in formation of pyridine carboxylic acids. V<sub>2</sub>O<sub>5</sub>-rutile in the process of oxidation of 4-methylpyridine on the catalyst forms the mixture of isonicotinic acid and its aldehyde. Connection between the dissociation rate of V<sub>2</sub>O<sub>5</sub> in catalysts of V<sub>2</sub>O<sub>5</sub>-anatase and V<sub>2</sub>O<sub>5</sub>-rutile and their activity in isomeric methylpyridines oxidation was established. High surface area, anatase structure of titanium are the key parameters determining the activity and selectivity of vanadium-titanium oxidation catalysts.</p>

Characterization of GaAs/AlGaAs quantum wells and quantum wires by chemical lattice imaging

1994 ◽  
Vol 52 ◽  
pp. 736-737
Author(s):  
A. Carlsson ◽  
J.-O. Malm ◽  
A. Gustafsson
Keyword(s):  
Quantum Well ◽  
Quantum Wells ◽  
Quantum Wires ◽  
Vapour Phase ◽  
Quantitative Information ◽  
Lattice Imaging ◽  
Vapour Phase Epitaxy ◽  
Metalorganic Vapour Phase Epitaxy ◽  
High Resolution Images

In this study a quantum well/quantum wire (QW/QWR) structure grown on a grating of V-grooves has been characterized by a technique related to chemical lattice imaging. This technique makes it possible to extract quantitative information from high resolution images.The QW/QWR structure was grown on a GaAs substrate patterned with a grating of V-grooves. The growth rate was approximately three monolayers per second without growth interruption at the interfaces. On this substrate a barrier of nominally Al0.35 Ga0.65 As was deposited to a thickness of approximately 300 nm using metalorganic vapour phase epitaxy . On top of the Al0.35Ga0.65As barrier a 3.5 nm GaAs quantum well was deposited and to conclude the structure an additional approximate 300 nm Al0.35Ga0.65 As was deposited. The GaAs QW deposited in this manner turns out to be significantly thicker at the bottom of the grooves giving a QWR running along the grooves. During the growth of the barriers an approximately 30 nm wide Ga-rich region is formed at the bottom of the grooves giving a Ga-rich stripe extending from the bottom of each groove to the surface.

Development and Characterization of Amine-Clay Hybrid Adsorbents for CO2 Capture

2016 ◽  
Vol 1133 ◽  
pp. 547-551 ◽  
Author(s):  
Ali E.I. Elkhalifah ◽  
Mohammad Azmi Bustam ◽  
Azmi Mohd Shariff ◽  
Sami Ullah ◽  
Nadia Riaz ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Surface Area ◽  
Surface Properties ◽  
Molar Mass ◽  
Adsorption Ability ◽  
Stepwise Increase ◽  
Inverse Effect ◽  
Bet Method ◽  
Sodium Form

The present work aims at a better understanding of the influences of the intercalated mono-, di- and triethanolamines on the characteristics and CO2 adsorption ability of sodium form of bentonite (Na-bentonite). The results revealed that the molar mass of intercalated amines significantly influenced the structural and surface properties as well as the CO2 adsorption capacity of Na-bentonite. In this respect, a stepwise increase in the d-spacing of Na-bentonite with the molar mass of amine was recorded by XRD technique. However, an inverse effect of the molar mass of amine on the surface area was confirmed by BET method. CO2 adsorption experiments on amine-bentonite hybrid adsorbents showed that the CO2 adsorption capacity inversly related to the molar mass of amine at 25 ͦC and 101 kPa. Accordingly, Na-bentonite modified by monoethanolammonium cations adsorbed as high as 0.475 mmol CO2/g compared to 0.148 and 0.087 mmol CO2/g for that one treated with di- and triethanolammonium cations, respectively.

scholarly journals Functional and Molecular Characterization of the Halomicrobium sp. IBSBa Inulosucrase

2021 ◽  
Vol 9 (4) ◽  
pp. 749
Author(s):  
Gülbahar Abaramak ◽  
Jaime Ricardo Porras-Domínguez ◽  
Henry Christopher Janse van Rensburg ◽  
Eveline Lescrinier ◽  
Ebru Toksoy Öner ◽  
...  
Keyword(s):  
Molecular Characterization ◽  
Phylogenetic Analyses ◽  
Halophilic Archaea ◽  
Maximum Activity ◽  
Physiological Relevance ◽  
Health Related ◽  
Specific Alternative ◽  
Binding Groove ◽  
Native Host

Fructans are fructose-based (poly)saccharides with inulin and levan being the best-known ones. Thanks to their health-related benefits, inulin-type fructans have been under the focus of scientific and industrial communities, though mostly represented by plant-based inulins, and rarely by microbial ones. Recently, it was discovered that some extremely halophilic Archaea are also able to synthesize fructans. Here, we describe the first in-depth functional and molecular characterization of an Archaeal inulosucrase from Halomicrobium sp. IBSBa (HmcIsc). The HmcIsc enzyme was recombinantly expressed and purified in Escherichia coli and shown to synthesize inulin as proven by nuclear magnetic resonance (NMR) analysis. In accordance with the halophilic lifestyle of its native host, the enzyme showed maximum activity at very high NaCl concentrations (3.5 M), with specific adaptations for that purpose. Phylogenetic analyses suggested that Archaeal inulosucrases have been acquired from halophilic bacilli through horizontal gene transfer, with a HX(H/F)T motif evolving further into a HXHT motif, together with a unique D residue creating the onset of a specific alternative acceptor binding groove. This work uncovers a novel area in fructan research, highlighting unexplored aspects of life in hypersaline habitats, and raising questions about the general physiological relevance of inulosucrases and their products in nature.

scholarly journals Preparation and Characterization of the Sulfur-Impregnated Natural Zeolite Clinoptilolite for Hg(II) Removal from Aqueous Solutions

Processes ◽  
2021 ◽  
Vol 9 (2) ◽  
pp. 217
Author(s):  
Marin Ugrina ◽  
Martin Gaberšek ◽  
Aleksandra Daković ◽  
Ivona Nuić
Keyword(s):  
Chemical Modification ◽  
Aqueous Solutions ◽  
Specific Surface ◽  
Surface Area ◽  
Natural Zeolite ◽  
Contact Time ◽  
Liquid Ratio ◽  
X Ray ◽  
Solid Liquid

Sulfur-impregnated zeolite has been obtained from the natural zeolite clinoptilolite by chemical modification with Na2S at 150 °C. The purpose of zeolite impregnation was to enhance the sorption of Hg(II) from aqueous solutions. Chemical analysis, acid and basic properties determined by Bohem’s method, chemical behavior at different pHo values, zeta potential, cation-exchange capacity (CEC), specific surface area, X-ray powder diffraction (XRPD), scanning electron microscopy with energy-dispersive X-ray analysis (SEM-EDS), Fourier transform infrared spectroscopy (FTIR), as well as thermogravimetry with derivative thermogravimetry (TG-DTG) were used for detailed comparative mineralogical and physico-chemical characterization of natural and sulfur-impregnated zeolites. Results revealed that the surface of the natural zeolite was successfully impregnated with sulfur species in the form of FeS and CaS. Chemical modification caused an increase in basicity and the net negative surface charge due to an increase in oxygen-containing functional groups as well as a decrease in specific surface area and crystallinity due to the formation of sulfur-containing clusters at the zeolite surface. The sorption of Hg(II) species onto the sulfur-impregnated zeolite was affected by the pH, solid/liquid ratio, initial Hg(II) concentration, and contact time. The optimal sorption conditions were determined as pH 2, a solid/liquid ratio of 10 g/L, and a contact time of 800 min. The maximum obtained sorption capacity of the sulfur-impregnated zeolite toward Hg(II) was 1.02 mmol/g. The sorption mechanism of Hg(II) onto the sulfur-impregnated zeolite involves electrostatic attraction, ion exchange, and surface complexation, accompanied by co-precipitation of Hg(II) in the form of HgS. It was found that sulfur-impregnation enhanced the sorption of Hg(II) by 3.6 times compared to the natural zeolite. The leaching test indicated the retention of Hg(II) in the zeolite structure over a wide pH range, making this sulfur-impregnated sorbent a promising material for the remediation of a mercury-polluted environment.

scholarly journals A Rubisco-binding protein is required for normal pyrenoid number and starch sheath morphology inChlamydomonas reinhardtii

2019 ◽  
Vol 116 (37) ◽  
pp. 18445-18454 ◽  
Author(s):  
Alan K. Itakura ◽  
Kher Xing Chan ◽  
Nicky Atkinson ◽  
Leif Pallesen ◽  
Lianyong Wang ◽  
...  
Keyword(s):  
Surface Area ◽  
Structure And Function ◽  
Binding Motif ◽  
Starch Granules ◽  
Wild Type ◽  
Bisphosphate Carboxylase ◽  
Biophysical Mechanism ◽  
Mechanism Function ◽  
And Function

A phase-separated, liquid-like organelle called the pyrenoid mediates CO2fixation in the chloroplasts of nearly all eukaryotic algae. While most algae have 1 pyrenoid per chloroplast, here we describe a mutant in the model algaChlamydomonasthat has on average 10 pyrenoids per chloroplast. Characterization of the mutant leads us to propose a model where multiple pyrenoids are favored by an increase in the surface area of the starch sheath that surrounds and binds to the liquid-like pyrenoid matrix. We find that the mutant’s phenotypes are due to disruption of a gene, which we call StArch Granules Abnormal 1 (SAGA1) because starch sheath granules, or plates, in mutants lacking SAGA1 are more elongated and thinner than those of wild type. SAGA1 contains a starch binding motif, suggesting that it may directly regulate starch sheath morphology. SAGA1 localizes to multiple puncta and streaks in the pyrenoid and physically interacts with the small and large subunits of the carbon-fixing enzyme Rubisco (ribulose-1,5-bisphosphate carboxylase/oxygenase), a major component of the liquid-like pyrenoid matrix. Our findings suggest a biophysical mechanism by which starch sheath morphology affects pyrenoid number and CO2-concentrating mechanism function, advancing our understanding of the structure and function of this biogeochemically important organelle. More broadly, we propose that the number of phase-separated organelles can be regulated by imposing constraints on their surface area.

scholarly journals Partial purification and biochemical characterization of a new highly acidic NYSO laccase from Alcaligenes faecalis

2020 ◽  
Vol 18 (1) ◽  
Author(s):  
Soad A. Abdelgalil ◽  
Ahmad R. Attia ◽  
Reyed M. Reyed ◽  
Nadia A. Soliman
Keyword(s):  
Enzyme Activity ◽  
Sodium Dodecyl ◽  
Alcaligenes Faecalis ◽  
Maximum Activity ◽  
Sodium Oxalate ◽  
Partial Purification ◽  
Bromophenol Blue ◽  
Bromocresol Purple ◽  
Laccase Enzyme

Abstract Background Due to the multitude industrial applications of ligninolytic enzymes, their demands are increasing. Partial purification and intensive characterization of contemporary highly acidic laccase enzyme produced by an Egyptian local isolate designated Alcaligenes faecalis NYSO were studied in the present investigation. Results Alcaligenes faecalis NYSO laccase has been partially purified and intensively biochemically characterized. It was noticed that 40–60% ammonium sulfate saturation showed maximum activity. A protein band with an apparent molecular mass of ~ 50 kDa related to NYSO laccase was identified through SDS-PAGE and zymography. The partially purified enzyme exhibited maximum activity at 55 °C and pH suboptimal (2.5–5.0). Remarkable activation for enzyme activity was recognized after 10-min exposure to temperatures (T) 50, 60, and 70 °C; time elongation caused inactivation, where ~ 50% of activity was lost after a 7-h exposure to 60 °C. Some metal ions Cu2+, Zn2+, Co2+, Ni2+, Mn2+, Cd2+, Cr2+, and Mg2+ caused strong stimulation for enzyme activity, but Fe2+ and Hg2+ reduced the activity. One millimolar of chelating agents [ethylenediamine tetraacetic acid (EDTA), sodium citrate, and sodium oxalate] caused strong activation for enzyme activity. Sodium dodecyl sulfate (SDS), cysteine-HCl, dithiothreitol (DTT), β-mercaptoethanol, thioglycolic acid, and sodium azide caused strong inhibition for NYSO laccase activity even at low concentration. One millimolar of urea, imidazole, kojic acid, phenylmethylsulfonyl fluoride (PMSF), H2O2, and Triton X-100 caused activation. The partially purified NYSO laccase had decolorization activity towards different dyes such as congo red, crystal violet, methylene blue, fast green, basic fuchsin, bromophenol blue, malachite green, bromocresol purple eriochrome black T, and Coomassie Brilliant Blue R-250 with various degree of degradation. Also, it had a vast range of substrate specificity including lignin, but with high affinity towards p-anisidine. Conclusion The promising properties of the newly studied laccase enzyme from Alcaligenes faecalis NYSO strain would support several industries such as textile, food, and paper and open the possibility for commercial use in water treatment. It will also open the door to new applications due to its ligninolytic properties in the near future.

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