scholarly journals Synthesis of Benzil by Air Oxidation of Benzoin and M(Salen) Catalyst

2019 ◽  
pp. 1-8 ◽  
Author(s):  
Qiuxin Shen ◽  
Liting Xu ◽  
Yiyan Jiang ◽  
Ran Zheng ◽  
Yiping Zhang
Keyword(s):  
Catalytic Activity ◽  
High Performance ◽  
Low Cost ◽  
Catalytic Performance ◽  
Air Oxidation ◽  
Catalyst Recycling ◽  
Reaction Conditions ◽  
Salen Complex ◽  
1H Nuclear Magnetic Resonance ◽  
Optimum Reaction

Bis salicylaldehyde ethylenediamine Schiff base (Salen) and its complexes with three metal ions (Co2+, Ni2+, Zn2+) were prepared, and characterized by infrared spectroscopy(IR). Using air as oxygen source, the optimum reaction conditions for the catalytic oxidation of 0.05 mol benzoin by Co (Salen) were obtained by orthogonal test as follows: base KOH 2 g, catalyst 1.5 g, N, N-dimethylformamide(DMF) as solvent, reaction temperature 40 °C, reaction time 1 h. Under these conditions, the catalytic performances of different metal complexes were investigated. The catalytic activity of Co(Salen) was the best one, the yield of benzil was up to 93.6%, the number of Ni(Salen) and Zn(Salen) was 86.3% and 82.1%, respectively. The reused catalytic performance of M(Salen) complex was also studied. The catalytic activity of Co(Salen), Ni(Salen) and Zn(Salen) was stable after 4 times recycle, the yield of benzil was 71.4%, 63.3% and 57.4%, respectively, and it was easy for catalyst recycling. The oxidation product was certainly benzil with high purity according to the characterization results of melting point(MP), IR, high performance liquid chromatography(HPLC) and 1H nuclear magnetic resonance(1H NMR). Compared with the common synthetic method of benzil, this one has the advantages of friendly environment, low cost and easy operation. It is a simple and green way to synthesize benzoyl efficiently.

scholarly journals Evaluation of wet air oxidation variables for removal of organophosphorus pesticide malathion using Box-Behnken design

2016 ◽  
Vol 75 (3) ◽  
pp. 619-628 ◽  
Author(s):  
Melike Isgoren ◽  
Erhan Gengec ◽  
Sevil Veli
Keyword(s):  
Removal Efficiency ◽  
Applied Pressure ◽  
Organophosphorus Pesticide ◽  
Operating Conditions ◽  
Quadratic Model ◽  
Air Oxidation ◽  
Wet Air Oxidation ◽  
Reaction Conditions ◽  
Efficient Treatment ◽  
Optimum Reaction

This paper deals with finding optimum reaction conditions for wet air oxidation (WAO) of malathion aqueous solution, by Response Surface Methodology. Reaction conditions, which affect the removal efficiencies most during the non-catalytic WAO system, are: temperature (60–120 °C), applied pressure (20–40 bar), the pH value (3–7), and reaction time (0–120 min). Those were chosen as independent parameters of the model. The interactions between parameters were evaluated by Box-Behnken and the quadratic model fitted very well with the experimental data (29 runs). A higher value of R2 and adjusted R2 (>0.91) demonstrated that the model could explain the results successfully. As a result, optimum removal efficiency (97.8%) was obtained at pH 5, 20 bars of pressure, 116 °C, and 96 min. These results showed that Box–Behnken is a suitable design to optimize operating conditions and removal efficiency for non-catalytic WAO process. The EC20 value of raw wastewater was measured as 35.40% for malathion (20 mg/L). After the treatment, no toxicity was observed at the optimum reaction conditions. The results show that the WAO is an efficient treatment system for malathion degradation and has the ability of converting malathion to the non-toxic forms.

scholarly journals Hierarchical H-ZSM5 zeolites based on natural kaolinite as a high-performance catalyst for methanol to aromatic hydrocarbons conversion

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Ahmad Asghari ◽  
Mohammadreza Khanmohammadi Khorrami ◽  
Sayed Habib Kazemi
Keyword(s):  
Pore Size ◽  
Aromatic Hydrocarbons ◽  
High Performance ◽  
Low Cost ◽  
Direct Synthesis ◽  
Fixed Bed ◽  
Methanol Conversion ◽  
Catalytic Performance ◽  
Fixed Bed Reactor ◽  
Good Prospect

AbstractThe present work introduces a good prospect for the development of hierarchical catalysts with excellent catalytic performance in the methanol to aromatic hydrocarbons conversion (MTA) process. Hierarchical H-ZSM5 zeolites, with a tailored pore size and different Si/Al ratios, were synthesized directly using natural kaolin clay as a low-cost silica and aluminium resource. Further explored for the direct synthesis of hierarchical HZSM-5 structures was the steam assisted conversion (SAC) with a cost-effective and green affordable saccharide source of high fructose corn syrup (HFCS), as a secondary mesopore agent. The fabricated zeolites exhibiting good crystallinity, 2D and 3D nanostructures, high specific surface area, tailored pore size, and tunable acidity. Finally, the catalyst performance in the conversion of methanol to aromatic hydrocarbons was tested in a fixed bed reactor. The synthesized H-ZSM5 catalysts exhibited superior methanol conversion (over 100 h up to 90%) and selectivity (over 85%) in the methanol conversion to aromatic hydrocarbon products.

Carbon Dioxide Hydrogenation to Methanol over Cu/ZnO-SBA-15 Catalyst: Effect of Metal Loading

2017 ◽  
Vol 380 ◽  
pp. 151-160 ◽  
Author(s):  
Sara Faiz Hanna Tasfy ◽  
Noor Asmawati Mohd Zabidi ◽  
Maizatul Shima Shaharun ◽  
Duvvria Subbarao ◽  
Ahmed Elbagir
Keyword(s):  
Catalytic Activity ◽  
Carbon Source ◽  
Active Sites ◽  
Low Cost ◽  
Fixed Bed ◽  
Textural Properties ◽  
Catalytic Performance ◽  
Hydrogenation Reaction ◽  
Supported Metal Catalysts ◽  
Metal Loading

Utilization of CO2 as a carbon source to produce valuable chemicals is one of the important ways to reduce the global warming caused by increasing CO2 in the atmosphere. Supported metal catalysts are crucial to produce clean and renewable fuels and chemicals from the stable CO2 molecules. The catalytic conversion of CO2 into methanol is recently under increased scrutiny as an opportunity to be used as a low-cost carbon source. Therefore, a series of the bimetallic Cu/ZnO-based catalyst supported by SBA-15 were synthesized via an impregnation technique with different total metal loading and tested in the catalytic hydrogenation of CO2 to methanol. The morphological and textural properties of the synthesized catalysts were determined by transmission electron microscopy (TEM), temperature programmed desorption, reduction, oxidation and pulse chemisorption (TPDRO), and N2-adsorption. The CO2 hydrogenation reaction was performed in a microactivity fixed-bed system at 250oC, 2.25 MPa, and H2/CO2 ratio of 3. Experimental results showed that the catalytic structure and performance were strongly affected by the loading of the active site. Where, the catalytic activity, the methanol selectivity as well as the space-time yield increased with increasing the metal loading until it reaches the maximum values at a metal loading of 15 wt% while further addition of metal inhibits the catalytic performance. The higher catalytic activity of 14% and methanol selectivity of 92% was obtained over a Cu/ZnO-SBA-15 catalyst with a total bimetallic loading of 15 wt%. The excellent performance of 15 wt% Cu/ZnO-SBA-15 catalyst is attributed to the presence of well dispersed active sites with small particle size, higher Cu surface area, and lower catalytic reducibility.

A Novel NiCl2-CuCl2/HMOR Catalyst for Direct Vapor-Phase Carbonylation of Methanol

2013 ◽  
Vol 316-317 ◽  
pp. 983-986 ◽  
Author(s):  
Hai Xia Wang ◽  
Wen Wen Guo ◽  
Ling Jun Zhu
Keyword(s):  
High Activity ◽  
Methyl Iodide ◽  
Vapor Phase ◽  
Methanol Conversion ◽  
Catalytic Performance ◽  
Composite Catalyst ◽  
Reaction Conditions ◽  
Reaction Pressure ◽  
Methanol Carbonylation ◽  
Optimum Reaction

Direct vapor-phase methanol carbonylation, without any methyl iodide in the feed as a promoter, was carried out over NiCl2-CuCl2/HMOR catalysts. The results showed that NiCl2-CuCl2/HMOR catalysts exhibited high activity for methanol carbonylation. The optimum component of the composite catalyst was 5wt% NiCl2 and 15wt% CuCl2. In addition, the effects of reaction pressure and temperature on catalytic performance of 5%NiCl2-15%CuCl2/HMOR catalyst were investigated. It was revealed that methanol conversion of 84.2% and carbonylation selectivity of 73.5% could be obtained under the optimum reaction conditions of P=1.5MPa and T=623K.

scholarly journals Differential Degradation and Detoxification of an Aromatic Pollutant by Two Different Peroxidases

2017 ◽  
Author(s):  
Aysha Hamad Alneyadi ◽  
Iltaf Shah ◽  
Synan F. AbuQamar ◽  
Syed Salman Ashraf
Keyword(s):  
Organic Pollutants ◽  
High Performance ◽  
Degradation Products ◽  
Low Molecular Weight ◽  
Optimum Conditions ◽  
Reaction Conditions ◽  
Toxicological Evaluation ◽  
Sulforhodamine B ◽  
Optimum Reaction ◽  
First Time

Enzymatic degradation of organic pollutants is a new and promising remediation approach. Peroxidases are one of the most commonly used classes of enzymes to degrade organic pollutants. However, it is generally assumed that all peroxidases behave similarly and produce similar degradation products. In this study, we conducted detailed studies of the degradation of a model aromatic pollutant, Sulforhodamine B dye (SRB dye), using two peroxidases—soybean peroxidase (SBP) and chloroperoxidase (CPO). Our results show that these two related enzymes had different optimum conditions (pH, temperature, H2O2 concentration...etc.) for efficiently degrading SRB dye. High-performance liquid chromatography and LC-mass spectrometry analyses confirmed that both SBP and CPO transformed the SRB dye into low molecular weight intermediates. While most of the intermediates produced by the two enzymes were the same, the CPO treatment produced at least one different intermediate. Furthermore, toxicological evaluation using lettuce (Lactuca sativa) seeds demonstrated that the SBP-based treatment was able to eliminate the phytotoxicity of SRB dye, but the CPO-based treatment did not. Our results show, for the first time, that while both of these related enzymes can be used to efficiently degrade organic pollutants, they have different optimum reaction conditions and may not be equally efficient in detoxification of organic pollutants.

scholarly journals Fe3O4@chitosan-tannic acid bionanocomposite as a novel nanocatalyst for the synthesis of pyranopyrazoles

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Maryam Kamalzare ◽  
Mohammad Reza Ahghari ◽  
Mohammad Bayat ◽  
Ali Maleki
Keyword(s):  
Reaction Time ◽  
Tannic Acid ◽  
High Performance ◽  
Catalytic Performance ◽  
Natural Material ◽  
Magnetic Nanocatalyst ◽  
Reaction Conditions ◽  
One Pot ◽  
Short Reaction Time ◽  
High Yields

AbstractRecently magnetic nanocatalyst has attracted considerable attention because of its unique properties, including high performance, easy separation from the reaction mixture, and recyclability. In this study, a novel magnetic bionanocomposite was synthesized with chitosan and tannic acid as a natural material. The synthesized bionanocatalyst was characterized by essential analysis. Fe3O4@chitosan-tannic acid as a heterogeneous nanocatalyst was successfully applied to synthesize pyranopyrazole and its derivatives by a one-pot four-component reaction of malononitrile, ethyl acetoacetate, hydrazine hydrate, and various aromatic aldehyde. At the end of the reaction, the nanocatalyst was separated from the reaction mixture and was reused several times with no significant decrease in its catalytic performance. Simple purification of products, the ability for recovering and reusing the nanocatalyst, eco-friendliness, high yields of pure products, mild reaction conditions, short reaction time, non-toxicity, economically affordable are some of the advantages of using the fabricated nanocatalyst in the synthesis of pyranopyrazole.

Effect of Different Iron Sources on In-Situ Growth of Zeolitic Imidazolate Frameworks-8: For Efficient Oxygen Reduction Electrocatalysts

2021 ◽  
Vol 21 (10) ◽  
pp. 5319-5328
Author(s):  
Sha-Sha Luo ◽  
Yu-Meng Ma ◽  
Peng-Wei Li ◽  
Ming-Hua Tian ◽  
Qiao-Xia Li
Keyword(s):  
Catalytic Activity ◽  
High Temperature ◽  
Oxygen Reduction ◽  
High Performance ◽  
Low Cost ◽  
Three Dimensional ◽  
Precious Metals ◽  
High Catalytic Activity ◽  
Zeolitic Imidazolate Frameworks ◽  
Wide Range

Transition metal and nitrogen co-doped carbon-based catalysts (TM-N-C) have become the most promising catalysts for Pt/C due to their wide range of sources, low cost, high catalytic activity, excellent stability and strong resistance to poisoning, especially Fe–N–C metal-organic frameworks (MOFs), which are some of the most promising precursors for the preparation of Fe–N–C catalysts due to their inherent properties, such as their highly ordered three-dimensional framework structure, controlled porosity, and tuneable chemistry. Based on these, in this paper, different iron sources were added to synthesis a sort of zeolitic imidazole frameworks (ZIF-8). Then the imidazole salt in ZIF-8 was rearranged into high N-doped carbon by high-temperature pyrolysis to prepare the Fe–N–C catalyst. We studied the physical characteristics of the catalysts by different iron sources and their effects on the catalytic properties of the oxygen reduction reaction (ORR). From the point of morphology, various iron sources have a positive influence on maintaining the morphology of ZIF-8 polyhedron. Fe–N/C–Fe(NO3)3 has the same anion as zinc nitrate, and can maintain a polyhedral morphology after high-temperature calcination. It had the highest ORR catalytic activity compared to the other four catalyst materials, which proved that there is a certain relationship between morphology and performance. This paper will provide a useful reference and new models for the development of high-performance ORR catalysts without precious metals.

scholarly journals Surface Modifications of 2D-Ti3C2O2 by Nonmetal Doping for Obtaining High Hydrogen Evolution Reaction Activity: A Computational Approach

Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 161
Author(s):  
Fangtao Li ◽  
Xiaoxu Wang ◽  
Rongming Wang
Keyword(s):  
Catalytic Activity ◽  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
Active Sites ◽  
High Performance ◽  
Hydrogen Adsorption ◽  
Low Cost ◽  
Level Shift ◽  
High Hydrogen ◽  
Catalytic Active Sites

As a typical two-dimensional (2D) MXene, Ti3C2O2 has been considered as a potential material for high-performance hydrogen evolution reaction (HER) catalyst, due to its anticorrosion and hydrophilic surface. However, it is still a challenge to improve the Ti3C2O2 surficial HER catalytic activity. In this work, we investigated the HER activity of Ti3C2O2 after the surface was doped with S, Se, and Te by the first principles method. The results indicated that the HER activity of Ti3C2O2 is improved after being doped with S, Se, Te because the Gibbs free energy of hydrogen adsorption (ΔGH) is increased from −2.19 eV to 0.08 eV. Furthermore, we also found that the ΔGH of Ti3C2O2 increased from 0.182 eV to 0.08 eV with the doping concentration varied from 5.5% to 16.7%. The HER catalytic activity improvement of Ti3C2O2 is attributed to the local crystal structure distortion in catalytic active sites and Fermi level shift leads to the p-d orbital hybridization. Our results pave a new avenue for preparing a low-cost and high performance HER catalyst.

scholarly journals Catalytic Decomposition of Nitrogen Oxides by Bimetallic Catalysts Synthesized by Dielectric Barrier Discharge Plasma Technology

2018 ◽  
Vol 53 ◽  
pp. 01032
Author(s):  
Libin Shi ◽  
Suitao Qi ◽  
Tianyou Jiao ◽  
Jifeng Qu ◽  
Xiao Tan ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Atmospheric Pressure ◽  
Bimetallic Catalysts ◽  
High Performance ◽  
Cold Plasma ◽  
Low Cost ◽  
Catalytic Decomposition ◽  
High Dispersion ◽  
Metal Support Interaction ◽  
Barrier Discharge Plasma

Nitrous oxide (N2O) is a common greenhouse gas and urgent need to be contained. Direct catalytic decomposition of N2O by high activity catalyst into N2 and O2 is a low-cost and harmless method. Bimetallic catalysts show good catalytic activity in many classes of reactions, and plasma technologies, applied to prepare of catalyst, are considered to be a promising method. In our contribution, DBD cold plasma is applied to synthesize Rhodium and Cobalt bimetallic catalysts for catalytic N2O decomposition. The influence of cobalt and rhodium content on N2O decomposition activity shows that the optimal amount of metal is determined as 5wt. % cobalt and 0.5wt. % rhodium loaded on Al2O3. The best working voltage is determined as 18kV. The results indicated that the Rh/Al2O3 catalysts prepared by atmospheric-pressure DBD cold plasma showed smaller size and high dispersion of Rh particles, so that the metal-support interaction and the catalytic activity are enhanced. Atmospheric-pressure DBD cold plasma is proved to be an environmentally friendly and efficient method for preparing high performance Rhodium and Cobalt bimetallic catalysts for catalytic N2O decomposition.

Pretreatment of Herbicides Production Wastewater by Spherical Micro-Electrolysis Media

2013 ◽  
Vol 295-298 ◽  
pp. 1079-1083 ◽  
Author(s):  
Ling Zhang ◽  
Jing Liang Xie
Keyword(s):  
Reaction Time ◽  
Biological Treatment ◽  
Low Cost ◽  
Good Effect ◽  
Post Processing ◽  
Reaction Conditions ◽  
Effects Of Ph ◽  
Optimum Reaction ◽  
The Cost ◽  
Operation Cost

[Objective] The aim is to study the pretreatment effect of herbicides production wastewater by spherical micro-electrolysis media. [Method] Spherical micro-electrolysis media is preferred for the pretreatment of herbicides production wastewater and effects of PH, amount of media and reaction time on the pretreatment was investigated. The change of pre- and post-processing herbicides production wastewater was determined; the operation cost was also analyzed. [Result]The optimum reaction conditions are as follows: the PH was 3; the amount of media was 1.0kg/L wastewater; and the reaction time was 3.0h. Under the optimum reaction conditions, the removal of COD, Chromaticity and TP reached 26.3%, 86.4% and 95.6% respectively; BOD5/COD varied from 0.10 to 0.35, and the biodegradability was improved greatly; the cost of pretreatment was 1.0yuan/t, and it was lower than that of electrolysis. [Conclusion] The pretreatment of herbicides production wastewater by spherical micro-electrolysis media has good effect, low cost and no soiling hardening, so it provides a good foundation for subsequent biological treatment.

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