scholarly journals Combination of reduction with metallic sodium and adsorption with mesoporous materials for re-refining of used insulating oil via experimental design

2020 ◽  
Vol 3 (01) ◽  
pp. 27-40
Author(s):  
Amir Vahid*© ◽  
Masoud Sohrab Sohrab
Keyword(s):  
Contact Time ◽  
Acid Number ◽  
Oxidation Products ◽  
Metallic Sodium ◽  
Direct Reaction ◽  
Reaction Products ◽  
Used Oil ◽  
Surface Method ◽  
Ft Ir ◽  
Mcm 41

In this study oils used direct influence sodium metallic on oxidation products and refining with the Mesoporous silicate material (MCM-41) and also silicate absorbents was synthesized and functionalized with aluminum salt through wet impreghation method (18wt%Al-MCM-41) (36wt% Al-MCM-41). Physical and structural properties has been investigated by FT-IR, BET,XRD and FESEM methods which shows a succful synthesis of the nano porous material. First step for reducing acid number oil we used direct reaction beetwen sodium metalic and used oil, after this step refining used oil by MCM-41 abosrbent has done. The effect of some parameters such as contact time, temperature and the dosage  has been determined and optimized by respons surface method (RSM). The results show that acid number decrease obtained 150 ,60min and 200% of dosage. Optimum condation for absorbent reaction products and new oxidation products by MCM-41 obtained contact time of 120min temperature (120oC) and dosage 200% .

Synthesis of Fused Azo-linked acridine derivatives using MCM-41/Ag2S-RHA nanocomposite

2021 ◽  
Vol 18 ◽  
Author(s):  
Mohammad Nikpassand ◽  
Leila Zare Fekri ◽  
Afshin Pourahmad ◽  
Zeinab Jafarian
Keyword(s):  
Catalytic Activity ◽  
Reaction Time ◽  
High Efficiency ◽  
Reaction Products ◽  
Reaction Conditions ◽  
Acridine Derivatives ◽  
Elemental Analyses ◽  
Ft Ir ◽  
Azo Derivatives ◽  
Mcm 41

Introduction: In this study, the synthesis of azo-linked acridine by the reaction of dimedone and synthesized diazoaryl-(2-amino-5-(phenyl)methanone using Ag2S/RHA-MCM-41nanocomposite is reported. Materials and Methods: The synthesized catalyst was characterized by FT-IR, XRD, and SEM. According to the obtained results, Ag2S/RHA-MCM-41 nanocomposite exhibited high activity in the synthesis of azo-acridine derivatives based on desirable yields and reaction time. Products were prepared in 1.5-2 h and with 88-93% yield. In all the reactions, the catalyst could be easily removed and reused, and its catalytic activity was maintained after five uses and did not decrease significantly. The structures of all newly synthesized products were characterized by spectroscopic spectra (FT-IR, 1H NMR, 13C NMR) and elemental analyses. Results and Discussion: The results of the study showed that ionic liquid [DBU]OAc (entry 8) and MCM-41/Ag2S-RHA nanocomposite (entry 8) possessed better efficiency and shorter time than other reaction conditions. Conclusion: In this study, new azo-linked acridine derivatives were synthesized by the reaction of different azo derivatives and dimedone using MCM-41/Ag2S-RHA nanocomposite, and the reaction products were obtained in 1.5-2 h with an efficiency of 88-93%. The short reaction time and high efficiency of the obtained products indicated the high efficiency of this method. In all the reactions, MCM-41/Ag2S-RHA nanocomposite could be easily removed and reused. Its catalytic activity was maintained in the sample reaction after five runs and did not decrease significantly.

scholarly journals Chitosan Cross-Linking with Acetaldehyde Acetals

Biomimetics ◽  
2022 ◽  
Vol 7 (1) ◽  
pp. 10
Author(s):  
Alexander Pestov ◽  
Yuliya Privar ◽  
Arseny Slobodyuk ◽  
Andrey Boroda ◽  
Svetlana Bratskaya
Keyword(s):  
Chitosan Solution ◽  
Direct Reaction ◽  
Acetate Solution ◽  
Reaction Products ◽  
Acid Type ◽  
Ft Ir ◽  
Low Cytotoxicity ◽  
Ph Range ◽  
Selection Of

Here we demonstrate the possibility of using acyclic diethylacetal of acetaldehyde (ADA) with low cytotoxicity for the fabrication of hydrogels via Schiff bases formation between chitosan and acetaldehyde generated in situ from acetals in chitosan acetate solution. This approach is more convenient than a direct reaction between chitosan and acetaldehyde due to the better commercial availability and higher boiling point of the acetals. Rheological data confirmed the formation of intermolecular bonds in chitosan solution after the addition of acetaldehyde diethyl acetal at an equimolar NH2: acetal ratio. The chemical structure of the reaction products was determined using elemental analysis and 13C NMR and FT-IR spectroscopy. The formed chitosan-acetylimine underwent further irreversible redox transformations yielding a mechanically stable hydrogel insoluble in a broad pH range. The reported reaction is an example of when an inappropriate selection of acid type for chitosan dissolution prevents hydrogel formation.

Continuous Ozonation of Polycyclic Aromatic Hydrocarbons in Oil/Water-Emulsions and Biodegradation of Oxidation Products

1999 ◽  
Vol 40 (4-5) ◽  
pp. 107-114 ◽  
Author(s):  
A. Kornmüller ◽  
U. Wiesmann
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Biological Treatment ◽  
Reaction Rate ◽  
Oxidation Products ◽  
Direct Reaction ◽  
Biological Degradation ◽  
Polycyclic Aromatic ◽  
Oil Water ◽  
Treatment Step

The continuous ozonation of polycyclic aromatic hydrocarbons (PAH) was studied in a two stage ozonation system followed by serobic biological degradation. The highly condensed PAH benzo(e)pyrene and benzo(k)fluoranthene were oxidized selectiely in synthetic oil/water-emulsions. The influence of the ozone mass transfer gas-liquid on the reaction rate of benzo(k)fluoranthene was studied for process optimization. The dissolved ozone concentration is influenced by temperature to a higher degree than the reaction rate of PAH. In dependence on pH, PAH oxidation occurs by a direct reaction with ozone inside the oil droplets. Two main ozonation products of benzo(e)pyrene were quantified at different retention times during ozonation and their transformation could be shown in the biological treatment step.

Nano-ZrO2/TiO2 Impregnated Orange Wood Sawdust and Peach Stone Shell Adsorbents for Cr (VI) Removal

2020 ◽  
Vol 16 (7) ◽  
pp. 880-892
Author(s):  
Şerife Parlayıcı ◽  
Kübra Tuna Sezer ◽  
Erol Pehlivan
Keyword(s):  
Contact Time ◽  
Ph Value ◽  
Order Kinetic ◽  
Adsorption Parameters ◽  
Wood Sawdust ◽  
Adsorption Data ◽  
Langmuir Isotherm Model ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Equilibrium Status

Background: In this work, Cr (VI) adsorption on nano-ZrO2๏TiO2 impregnated orange wood sawdust (Zr๏Ti/OWS) and nano-ZrO2๏TiO2 impregnated peach stone shell (Zr๏Ti/PSS) was investigated by applying different adsorption parameters such as Cr (VI) concentrations, contact time, adsorbent dose, and pH for all adsorbents. Methods: The adsorbents were characterized by SEM and FT-IR. The equilibrium status was achieved after 120 min of contact time and optimum pH value around 2 were determined for Cr (VI) adsorption. Adsorption data in the equilibrium is well-assembled by the Langmuir model during the adsorption process. Results: Langmuir isotherm model showed a maximum adsorption value of OWS: 21.65 mg/g and Zr๏Ti/OWS: 27.25 mg/g. The same isotherm displayed a maximum adsorption value of PSS: 17.64 mg/g, and Zr๏Ti/PSS: 31.15 mg/g. Pseudo-second-order kinetic models (R2=0.99) were found to be the best models for describing the Cr (VI) adsorption reactions. Conclusıon: Thermodynamic parameters such as changes in ΔG°, ΔH°, and ΔS° have been estimated, and the process was found to be spontaneous.

scholarly journals Release of toxic methylene blue from water by mesoporous silicalite-1: characterization, kinetics and isotherm studies

2021 ◽  
Vol 11 (7) ◽  
Author(s):  
Sabarish Radoor ◽  
Jasila Karayil ◽  
Aswathy Jayakumar ◽  
Jyotishkumar Parameswaranpillai ◽  
Suchart Siengchin
Keyword(s):  
Electron Microscopy ◽  
Contact Time ◽  
Dye Removal ◽  
Batch Adsorption ◽  
Aqueous Environment ◽  
Order Kinetic ◽  
Adsorption Method ◽  
X Ray ◽  
Ft Ir ◽  
Adsorption Desorption

AbstractIn the present work, we have developed a mesoporous silicalite-1 using CMC as a template for the removal of MB from aqueous solution. The synthesized silicalite-1 were characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), Energy-dispersive X-ray spectroscopy (EDAX) and N2 adsorption–desorption isotherm (BET). XRD and FT-IR analysis confirmed the formation of crystallinity and development of MFI structure in the mesoporous silicalite-1. The adsorption of MB dye on mesoporous silicalite-1 was conducted by batch adsorption method. The effect of various parameters such as adsorbent dosage, initial dye concentration, contact time and temperature on the dye uptake ability of silicalite-1 was investigated. The operating parameters for the maximum adsorption are silicalite-1 dosage (0.1 wt%), contact time (240 min), initial dye concentration (10 ppm) and temperature (30 ℃). The MB dye removal onto mesoporous silicalite-1 followed pseudo-second-order kinetic and Freundlich isotherm. The silicalite-1 exhibits 86% removal efficiency even after six adsorption–desorption cycle. Therefore, the developed mesoporous silicalite-1 is an effective eco-friendly adsorbent for MB dye removal from aqueous environment.

scholarly journals Potential-pH diagrams considering complex oxide solution phases for understanding aqueous corrosion of multi-principal element alloys

2020 ◽  
Vol 4 (1) ◽  
Author(s):  
Kang Wang ◽  
Junsoo Han ◽  
Angela Yu Gerard ◽  
John R. Scully ◽  
Bi-Cheng Zhou
Keyword(s):  
Solid Solution ◽  
Free Energy ◽  
Graphical Representation ◽  
Equilibrium Composition ◽  
Complex Oxide ◽  
Oxidation Products ◽  
Reaction Products ◽  
Aqueous Corrosion ◽  
Principal Element ◽  
Diagram Method

AbstractThe potential-pH diagram, a graphical representation of the thermodynamically predominant reaction products in aqueous corrosion, is originally proposed for the corrosion of pure metals. The original approach only leads to stoichiometric oxides and hydroxides as the oxidation products. However, numerous experiments show that non-stoichiometric oxide scales are prevalent in the aqueous corrosion of alloys. In the present study, a room temperature potential-pH diagram considering oxide solid solutions, as a generalization of the traditional potential-pH diagram with stoichiometric oxides, is constructed for an FCC single-phase multi-principal element alloy (MPEA) based on the CALculation of PHAse Diagram method. The predominant reaction products, the ions in aqueous solution, and the cation distribution in oxides are predicted. The oxide solid solution is stabilized by the mixing free energy (or mixing entropy) and the stabilizing effect becomes more significant as the temperature increases. Consequently, solid solution oxides are stable in large regions of the potential-pH diagram and the mixing free energy mostly affects the equilibrium composition of the stable oxides, while the shape of stable regions for oxides is mostly determined by the structure of the stable oxides. Agreements are found for Ni2+, Fe2+, and Mn2+ between the atomic emission spectroelectrochemistry measurements and thermodynamic calculations, while deviations exist for Cr3+ and Co2+ possibly due to surface complexation with species such as Cl− and the oxide dissolution. By incorporating the solution models of oxides, the current work presents a general and more accurate way to analyze the reaction products during aqueous corrosion of MPEAs.

scholarly journals Magnetically recoverable nanostructured Pd complex of dendrimeric type ligand on the MCM-41: Preparation, characterization and catalytic activity in the Heck reaction

2020 ◽  
Vol 43 (1) ◽  
pp. 184-199
Author(s):  
Mohammad Abdollahi-Alibeik ◽  
Najmeh Gharibpour ◽  
Zahra Ramazani
Keyword(s):  
Heck Reaction ◽  
Palladium Complex ◽  
Nanostructured Material ◽  
Magnetic Core ◽  
Aryl Halides ◽  
Heterogeneous Samples ◽  
Recoverable Catalyst ◽  
Ft Ir ◽  
Magnetically Recoverable Catalyst ◽  
Mcm 41

AbstractA palladium complex of a dendrimer type ligand of aminoethylacrylamide immobilized onto the mesoporous channels of MCM-41 with magnetic core was prepared and characterized using various techniques such as XRD, TEM, BET, FT-IR, TGA, and VSM. The prepared nanostructured material was found as a magnetically recoverable catalyst for Heck reaction of aryl halides and vinylic C–H. The catalyst is easily recoverable with an external magnet and is reusable with different leaching amounts depending to loading of Pd. A hot filtration test was also performed and gave evidence that Palladium in heterogeneous samples can dissolve and then redeposit on the surface of the support material.

FT-IR studies on the acidity of gallium-substituted mesoporous MCM-41 silica

2004 ◽  
Vol 85 (1) ◽  
pp. 145-150 ◽  
Author(s):  
Gemma Turnes Palomino ◽  
Juan José Cuart Pascual ◽  
Montserrat Rodrı́guez Delgado ◽  
José Bernardo Parra ◽  
Carlos Otero Areán
Keyword(s):  
Ir Studies ◽  
Ft Ir ◽  
Mcm 41

scholarly journals Removal of anionic surfactants by sorption onto Aminated Mesoporous Carbon

2013 ◽  
Vol 19 (3) ◽  
pp. 347-357 ◽  
Author(s):  
S.E. Moradi ◽  
J. Khodaveisy ◽  
R. Dashti
Keyword(s):  
Contact Time ◽  
Mesoporous Carbon ◽  
Anionic Surfactants ◽  
Textural Properties ◽  
Nitrogen Adsorption ◽  
Langmuir Model ◽  
Carbon Adsorbents ◽  
Solution Ph ◽  
Batch Mode ◽  
Ft Ir

Direct and indirect releases of large quantities of surfactants to the environment may result in serious health and environmental problems. Therefore, surfactants should be removed from water before release to the environment or delivery for public use. In the present work, the removal of anionic surfactants, benzene sulfonate (BS), p-toluene sulfonate (TS) and 4-octylbenzene sulfonate (OBS) from water by adsorption onto Amino modified mesoporous carbon (AMC) were studied. The AMC surface chemistry and textural properties was characterized by nitrogen adsorption, XRD and FT-IR analyses. Experiments were conducted in batch mode with the variables such as amount of contact time, solution pH, dose of adsorbent and temperature. Finally, the adsorption isotherms of anionic surfactants on mesoporous carbon adsorbents were in agreement with a Langmuir model. AMC has shown higher anionic surfactants adsorption capacity than the untreated mesoporous carbon, which can explain by strong interaction between anionic surfactant and cationic surface of adsorbent.

scholarly journals Thermodynamic simulation of oxidation process of the Moss-Mo3Si hypoeutectic alloy, doped with scandium or neodymium

2019 ◽  
Vol 57 (2) ◽  
pp. 90-100
Author(s):  
Alexey V. Larionov ◽  
◽  
Ludmila Y. Udoeva ◽  
Vladimir M. Chumarev ◽  
◽  
...  
Keyword(s):  
Oxidation Process ◽  
Thermodynamic Simulation ◽  
Oxidation Products ◽  
Hypoeutectic Alloy ◽  
Protective Film ◽  
Chemical Transformations ◽  
Reaction Products ◽  
Moist Air ◽  
Condensed Product ◽  
Hsc Chemistry

In order to study the effect of yttrium additives on the oxidation of molybdenum silicide alloys, thermodynamic modeling of the interaction in Mo-Mo3Si-Sc5Si3 и Mo-Mo3Si-NdSi systems with dry and moist air was performed in the temperature range 25-2000 °C. The calculations were performed using the HSC Chemistry 6.12 software, into the database of which the calculated missing thermochemical characteristics silicates, molybdates of scandium and neodymium were entered. Based on the obtained dependences of the composition of phases on temperature and charge of the oxidant (air or vapor-air mixture), the sequence of phase formation was determined and the compositions of oxidation products were estimated. It is shown that, under equilibrium conditions, the oxidation process with dry and moist air proceeds almost equally, since the interaction of the components of the alloy with oxygen is thermodynamically preferable than with water vapor. According to the obtained thermodynamic models, the oxidation process of the Mo-5Si-3(Sc, Nd) (wt.%) alloys involves a sequence of the following chemical transformations: at the beginning Mo and Sc (Nd) silicides oxidize forming Sc2O3 ( Nd2O3), SiO2 and elemental Mo, then molybdenum is oxidized to MoO2 and Sc2O3 or Nd2O3 interacts with SiO2 with the formation of appropriate silicates Sc2Si2O7 или Nd2Si2O7. As a result of the complete oxidation of the alloy, MoO3 and Sc2(MoO4)3 or Nd2Mo4O15 are added to the condensed product, and molybdenum oxide (MoO3)n vapor appears in the gas phase. In addition, the formation of Nd2Mo2O7 and Nd2 (MoO4)3 is possible. During the oxidation of the Mo-5Si-3Nd alloy at T> 1700 oC, Nd(OH)3 can be formed in the condensed reaction products. According to the results of complete thermodynamic analysis, the formation of silicates and molybdates of scandium and neodymium can promote to the formation of a protective film on the surface of the alloys, which limits the diffusion of oxygen in them, and as a result, the oxidation resistance of alloys should increase.

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