scholarly journals PHENOL removal in refinery wastewater using mixed oxides prepared by green synthesis

2021 ◽  
Author(s):  
Fatai Alade Aderibigbe ◽  
◽  
Tunmise Latifat Adewoye ◽  
Sherif Ishola Mustapha ◽  
Ishaq Alhassan Mohammed ◽  
...  
Keyword(s):  
Green Synthesis ◽  
Mixed Oxide ◽  
Environmental Remediation ◽  
High Performance ◽  
Mixed Oxides ◽  
Phenol Concentration ◽  
Phenol Removal ◽  
X Ray ◽  
Piliostigma Thonningii ◽  
Process Wastewater

Mixed solid oxides are known for their excellent catalytic property and applications in environmental remediation. This study presents a green-synthesis route for magnesium oxide–titanium oxide, a mixed oxide here demonstrated to possess high performance of phenol removal from hydrocarbon refinery process wastewater. Mixed oxide (MgO-TiO2) was prepared by using the whole extract from leaves of Piliostigma Thonningii as reducing agent. A structural attribute of the mixed oxide was investigated using X-ray Diffractometer, High-Resolution Scanning Electronic Microscopy and Energy Dispersive X-ray. Petroleum refinery raw wastewater having phenol concentration of 19.961 mg/L was treated using the green-synthesized mixed oxide. Adsorptive phenols removal up to 99.5% was achieved with a dosage of 0.04 g/100 mL at temperature of 35 °C, and contact time of 1.167 h. By this, the treated water meets the standard acceptable phenol concentration (0.1 mg/L) in wastewater of hydrocarbon refinery.

scholarly journals Effect of Mg/Al molar ratio on the basicity of Mg-Al mixed oxide derived from Mg-Al hydrotalcite

2020 ◽  
Vol 10 (6) ◽  
pp. 625
Author(s):  
Said Arhzaf ◽  
Mohammed Naciri Bennani ◽  
Sadik Abouarnadasse ◽  
Hamid Ziyat ◽  
Omar Qabaqous
Keyword(s):  
Thermal Analysis ◽  
Mixed Oxide ◽  
Mixed Oxides ◽  
Molar Ratio ◽  
Acid Molecule ◽  
X Ray Diffraction ◽  
Phenol Adsorption ◽  
X Ray ◽  
Maximum Quantity ◽  
Uv Visible

<p>The fundamental character of the Mg-Al mixed oxide (Mg<sub>n</sub>(Al)O), derived from the Mg-Al hydrotalcite (Mg<sub>n</sub>Al-CO<sub>3</sub>-HT), where n corresponds to the Mg/Al molar ratio (n: 2, 2.5, 3, 3.5 and 4), was studied by using the adsorption of phenol as a probe acid molecule. The hydrotalcite precursors were prepared by the coprecipitation method. Their derived mixed oxides were obtained by thermal treatment at 450°C in a flow of air. The resulting solids were characterized by X-ray fluorescence spectroscopy (XRF), X-ray diffraction (XRD), infrared spectroscopy (FTIR), thermogravimetric and differential thermal analysis             (TG-DTA), nitrogen physisorption (BET) and phenol chemisorption. The phenol adsorption followed by UV-Visible spectrophotometry shows that the basicity increases with the Mg/Al molar ratio, such that maximum quantity of phenol adsorbed (Q<sub>ads</sub> = 0.54 mmol/g <sub>cat</sub>) was obtained with the mixed oxide derived from the Mg-Al hydrotalcite of Mg/Al molar ratio equal to 3.5.</p>

scholarly journals Highly Active Transition Metal-Promoted CuCeMgAlO Mixed Oxide Catalysts Obtained from Multicationic LDH Precursors for the Total Oxidation of Methane

Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 613
Author(s):  
Hussein Mahdi S. Al-Aani ◽  
Mihaela M. Trandafir ◽  
Ioana Fechete ◽  
Lucia N. Leonat ◽  
Mihaela Badea ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transition Metal ◽  
Mixed Oxide ◽  
Mixed Oxides ◽  
Catalytic Performance ◽  
Atomic Ratio ◽  
Total Oxidation ◽  
X Ray ◽  
Oxidation Of Methane ◽  
Al2o3 Catalyst

To improve the catalytic performance of an active layered double hydroxide (LDH)-derived CuCeMgAlO mixed oxide catalyst in the total oxidation of methane, it was promoted with different transition-metal cations. Thus, two series of multicationic mixed oxides were prepared by the thermal decomposition at 750 °C of their corresponding LDH precursors synthesized by coprecipitation at constant pH of 10 under ambient atmosphere. The first series of catalysts consisted of four M(3)CuCeMgAlO mixed oxides containing 3 at.% M (M = Mn, Fe, Co, Ni), 15 at.% Cu, 10 at.% Ce (at.% with respect to cations), and with Mg/Al atomic ratio fixed to 3. The second series consisted of four Co(x)CuCeMgAlO mixed oxides with x = 1, 3, 6, and 9 at.% Co, while keeping constant the Cu and Ce contents and the Mg/Al atomic ratio. All the mixed oxides were characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) coupled with X-ray energy dispersion analysis (EDX), X-ray photoelectron spectroscopy (XPS), nitrogen adsorption-desorption at −196 °C, temperature-programmed reduction under hydrogen (H2-TPR), and diffuse reflectance UV-VIS spectroscopy (DR UV-VIS), while thermogravimetric and differential thermal analyses (TG-DTG-DTA) together with XRD were used for the LDH precursors. The catalysts were evaluated in the total oxidation of methane, a test reaction for volatile organic compounds (VOC) abatement. Their catalytic performance was explained in correlation with their physicochemical properties and was compared with that of a reference Pd/Al2O3 catalyst. Among the mixed oxides studied, Co(3)CuCeMgAlO was found to be the most active catalyst, with a temperature corresponding to 50% methane conversion (T50) of 438 °C, which was only 19 °C higher than that of a reference Pd/Al2O3 catalyst. On the other hand, this T50 value was ca. 25 °C lower than that observed for the unpromoted CuCeMgAlO system, accounting for the improved performance of the Co-promoted catalyst, which also showed a good stability on stream.

Formation of mixed oxide powders in flames: Part II. SiO2−GeO2 and Al2O3−TiO2

1992 ◽  
Vol 7 (7) ◽  
pp. 1870-1875 ◽  
Author(s):  
Cheng-Hung Hung ◽  
Philippe F. Miquel ◽  
Joseph L. Katz
Keyword(s):  
Light Scattering ◽  
Mixed Oxide ◽  
Mixed Oxides ◽  
Electrophoretic Method ◽  
X Ray ◽  
Oxide Powders ◽  
Flame Burner ◽  
Carbon Coated ◽  
Oxide Particles ◽  
Counterflow Diffusion Flame

SiO2−GeO2 and Al2O3−TiO2 mixed oxide powders were synthesized using a counterflow diffusion flame burner. SiCl4, GeCl4, Al(CH3)3, and TiCl4 were used as source materials for the formation of oxide particles in hydrogen-oxygen flames. In situ particle sizes were determined using dynamic light-scattering. Powders were collected using two different methods, a thermophoretic method (particles are collected onto carbon coated TEM grids) and an electrophoretic method (particles are collected onto stainless steel strips). Their size, morphology, and crystalline form were examined using a transmission electron microscope and an x-ray diffractometer. A photomultiplier at 90° to the argon ion laser beam was used to measure the light-scattering intensity. The formation of the mixed oxides was investigated using Si to Ge and Al to Ti ratios of 3:5 and 1:1, respectively. Heterogeneous nucleation of the SiO2 on the surface of the GeO2 was observed. In Al2O3−TiO2 mixtures, both oxide particles form at the same temperature. X-ray diffraction analysis of particles sampled at temperatures higher than 1553 K showed the presence of rutile, γ–Al2O3, and aluminum titanate. Although the particle formation process for SiO2−GeO2 is very different from that for Al2O3−TiO2, both mixed oxides result in very uniform mixtures.

scholarly journals Effect of Sr on the properties of Ce-Zr-La mixed oxides

2006 ◽  
Vol 71 (3) ◽  
pp. 285-291 ◽  
Author(s):  
Richuan Rao ◽  
LI Lianyong ◽  
LI Fengyi
Keyword(s):  
Mixed Oxide ◽  
Storage Capacity ◽  
Mixed Oxides ◽  
Sol Gel ◽  
Oxygen Storage Capacity ◽  
Oxygen Storage ◽  
X Ray Diffraction ◽  
Pulse Technique ◽  
X Ray ◽  
Good Thermal Stability

Ce-Zr-La-Sr mixed oxides, with different Sr contents, were prepared by the sol-gel method. In a flow-system microreactor, the reduction properties and the oxygen storage capacity (OSC) of the Ce-Zr-La-Sr mixed oxides were investigated by a temperature programmed reduction (TPR) and a pulse technique. It was shown that the properties of the Ce-Zr-La mixed oxides depend on the Sr content and that the optimum Sr content in the Ce-Zr-La-Sr mixed oxide is 3 mol%. The Ce-Zr-La-Sr mixed oxides doped with 3 mol% Sr (Ce0.52Zr0.4La0.05Sr0.03O1.945) has the largest specific surface area and better reduction properties and oxygen storage capacity in comparison to the other investigated samples. The XRD results of the Ce-Zr-La-Sr mixed oxides showed that their X-ray diffraction patterns are well in agreement with that of fluorite-type CeO2 with Sr ions incorporated into the Ce-Zr-La mixed oxide structures. With increasing calcination temperature, the intensity of the X-ray diffraction peaks increased, but no new peaks were observed. All of these indicate that the synthesized samples had good thermal stability.

scholarly journals High Performance of Mn-Doped MgAlOx Mixed Oxides for Low Temperature NOx Storage and Release

Catalysts ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 677 ◽  
Author(s):  
Cui ◽  
Ma ◽  
Wang ◽  
Liu ◽  
Liu ◽  
...  
Keyword(s):  
Low Temperature ◽  
High Performance ◽  
Storage Capacity ◽  
Mixed Oxides ◽  
Nox Storage ◽  
X Ray ◽  
Temperature Range ◽  
Nox Storage Capacity ◽  
Nox Adsorption ◽  
Mn Doped

NOx storage-reduction (NSR) is a potential approach for the effective removal of NOx under the lean conditions in lean-burn engines. Herein, manganese-doped mixed oxides (Mn/MgAlOx) with high performance for low temperature NOx storage and release were derived from hydrotalcites precursors prepared by a facile coprecipitation method. The catalysts were characterized by X-ray diffraction (XRD), SEM, N2 adsorption-desorption, H2-TPR, FT-IR, and X-ray photoelectron spectroscopy (XPS) techniques. The Mn-doped MgAlOx catalysts exhibited high NOx storage capacity (NSC) at low temperature range (150–300 °C), which was related to their increased surface area, improved reducibility and higher surface Mn3+ content. The largest NSC measured, 426 μmol/g, was observed for NOx adsorption at 200 °C on Mn15 catalyst (the sample containing 15 wt% of Mn). The in situ DRIFTS spectra of NOx adsorption proved that the Mn-doped hydrotalcite catalysts are preferred for low temperature NOx storage and release due to their ability to store NOx mainly in the form of thermally labile nitrites. NSR cycling tests revealed the NOx removal rate of Mn15 sample can reach above 70% within the wide temperature range of 150–250 °C. Besides, the influence of CO2, soot, H2O and SO2 on NOx storage performance of Mn15 catalyst was also studied. In all, owning to their excellent NOx storage capacity, NSR cycling performance, and resistance to CO2, soot, SO2 and H2O, the Mn-doped MgAlOx NSR catalysts have broad application prospects in NOx control at low temperatures.

scholarly journals Magnesium Effect in K/Co-Mg-Mn-Al Mixed Oxide Catalyst for Direct NO Decomposition

Catalysts ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 931
Author(s):  
Kateřina Karásková ◽  
Kateřina Pacultová ◽  
Anna Klegova ◽  
Dagmar Fridrichová ◽  
Marta Valášková ◽  
...  
Keyword(s):  
Mixed Oxide ◽  
Thermal Instability ◽  
Mixed Oxides ◽  
No Decomposition ◽  
Molar Ratio ◽  
Partial Substitution ◽  
X Ray ◽  
Mixed Oxide Catalyst ◽  
Temperature Programmed ◽  
Activity Decrease

Emission of nitric oxide represents a serious environmental problem since it contributes to the formation of acid rain and photochemical smog. Potassium-modified Co-Mn-Al mixed oxide is an effective catalyst for NO decomposition. However, there are problems related to the thermal instability of potassium species and a high content of toxic and expensive cobalt. The reported research aimed to determine whether these shortcomings can be overcome by replacing cobalt with magnesium. Therefore, a series of Co-Mg-Mn-Al mixed oxides with different Co/Mg molar ratio and promoted by various content of potassium was investigated. The catalysts were thoroughly characterized by atomic absorption spectroscopy (AAS), temperature-programmed reduction by hydrogen (TPR-H2), temperature-programmed desorption of CO2 (TPD-CO2), X-ray powder diffraction (XRD), N2 physisorption, species-resolved thermal alkali desorption (SR-TAD), and tested in direct NO decomposition with and without the addition of oxygen and water vapor. Partial substitution of magnesium for cobalt did not cause an activity decrease when the optimal molar ratio of K/Co on the normalized surface area was maintained; it means that the portion of expensive and toxic cobalt can be successfully replaced by magnesium without any decrease in catalytic activity.

Kinetic and structural studies of oxygen availability of the mixed oxides Pr1–xMxOy (M = Ce, Zr)

1996 ◽  
Vol 11 (8) ◽  
pp. 1960-1971 ◽  
Author(s):  
M. Yu. Sinev ◽  
G. W. Graham ◽  
L. P. Haack ◽  
M. Shelef
Keyword(s):  
Gas Phase ◽  
Mixed Oxide ◽  
Photoelectron Spectroscopy ◽  
Mixed Oxides ◽  
Structural Features ◽  
Redox Processes ◽  
Structural Studies ◽  
X Ray ◽  
Speed Up ◽  
Kinetics Of

One composition of Pr–Ce mixed oxide and a range of compositions of Pr–Zr mixed oxide were prepared by coprecipitation methods and characterized by x-ray powder diffraction, thermogravimetric analysis, and x-ray photoelectron spectroscopy. Based on phases formed, the PrOy—ZrO2 system in an oxygen-containing atmosphere at moderate temperatures (up to 800–1000 °C) is analogous to that of CeO2–ZrO2. Addition of either Ce or Zr to pure Pr oxide affects both the total amount of oxygen that can be reversibly exchanged between oxide and gas phase and the kinetics of the redox processes. Ce dramatically increases the amount (per Pr atom) and lowers the temperature of exchange, Zr slightly decreases the amount and also lowers the temperature of exchange, and both modifiers speed up the rate. These observations are rationalized in terms of bulk and surface structural features of the mixed oxides.

Synthesis, Characterization and Study of the Photocatalytic Activity of the Ti/Fe Mixed Oxide

2014 ◽  
Vol 17 (2) ◽  
Author(s):  
Franciély Ignachewski ◽  
Eryza G. de Castro ◽  
Fauze J. Anaissi ◽  
Sérgio T. Fujiwara
Keyword(s):  
Photocatalytic Activity ◽  
Titanium Oxide ◽  
Mixed Oxide ◽  
Mixed Oxides ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Gel Method ◽  
X Ray ◽  
Sol Gel Method

AbstractThe mixed oxides of Ti/Fe were prepared by sol-gel method and the materials were synthesized with different Ti/Fe ratios (0, 25, 50 and 75 wt% of iron). In the spectrum of the material without iron, it is possible to observe the predominant phase of the titanium oxide was anatase, which can be confirmed through x-ray diffraction. It can be observed that when the iron was added, the predominant phase of the titanium oxide was rutile and was found evidence of the formation of pseudobrookite (Fe

Macroprobe Mode for the Study of Segregation in Steels

1990 ◽  
Vol 48 (2) ◽  
pp. 260-261
Author(s):  
Auclair Gilles ◽  
Benoit Danièle
Keyword(s):  
Mechanical Properties ◽  
Spatial Distribution ◽  
High Performance ◽  
Volume Fraction ◽  
Sheet Steel ◽  
Acquisition Time ◽  
Chemical Information ◽  
X Ray ◽  
Accurate Quantitative Analysis ◽  
Optical Micrographs

During these last 10 years, high performance correction procedures have been developed for classical EPMA, and it is nowadays possible to obtain accurate quantitative analysis even for soft X-ray radiations. It is also possible to perform EPMA by adapting this accurate quantitative procedures to unusual applications such as the measurement of the segregation on wide areas in as-cast and sheet steel products.The main objection for analysis of segregation in steel by means of a line-scan mode is that it requires a very heavy sampling plan to make sure that the most significant points are analyzed. Moreover only local chemical information is obtained whereas mechanical properties are also dependant on the volume fraction and the spatial distribution of highly segregated zones. For these reasons we have chosen to systematically acquire X-ray calibrated mappings which give pictures similar to optical micrographs. Although mapping requires lengthy acquisition time there is a corresponding increase in the information given by image anlysis.

PHAX-SCAN: Functional integration of a Scanning Electron Microscope and an energy-dispersive x-ray analyser

1989 ◽  
Vol 47 ◽  
pp. 56-57
Author(s):  
Marc H. Peeters ◽  
Max T. Otten
Keyword(s):  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
High Speed ◽  
High Performance ◽  
Functional Integration ◽  
Energy Dispersive ◽  
X Rays ◽  
X Ray ◽  
High Speed Analysis ◽  
Scanning Electron

Over the past decades, the combination of energy-dispersive analysis of X-rays and scanning electron microscopy has proved to be a powerful tool for fast and reliable elemental characterization of a large variety of specimens. The technique has evolved rapidly from a purely qualitative characterization method to a reliable quantitative way of analysis. In the last 5 years, an increasing need for automation is observed, whereby energy-dispersive analysers control the beam and stage movement of the scanning electron microscope in order to collect digital X-ray images and perform unattended point analysis over multiple locations.The Philips High-speed Analysis of X-rays system (PHAX-Scan) makes use of the high performance dual-processor structure of the EDAX PV9900 analyser and the databus structure of the Philips series 500 scanning electron microscope to provide a highly automated, user-friendly and extremely fast microanalysis system. The software that runs on the hardware described above was specifically designed to provide the ultimate attainable speed on the system.

Sign in / Sign up

Export Citation Format

Share Document