Formation of ruthenium nanoparticles inside aluminosilicate nanotubes and their catalytic activity in aromatics hydrogenation: the impact of complexing agents and reduction procedure

2020 ◽  
Vol 92 (6) ◽  
pp. 909-918 ◽  
Author(s):  
Anna Stavitskaya ◽  
Aleksandr Glotov ◽  
Kristina Mazurova ◽  
Vladimir Nedolivko ◽  
Pavel Gushchin ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Ethylenediaminetetraacetic Acid ◽  
Halloysite Nanotubes ◽  
Complexing Agents ◽  
Benzene Hydrogenation ◽  
Ruthenium Nanoparticles ◽  
Reduction Procedure ◽  
The Impact ◽  
Acetone Azine ◽  
Thermal Stability Of

AbstractRuthenium particles with size from 1 to 7 nm were formed by reduction of ruthenium complexes with urea, ethylenediaminetetraacetic acid, acetone azine, 1,2-Bis(2-furylmethylene)hydrazine) inside halloysite nanotubes. Catalysts of different morphology with Ru content from 0.75 to 0.93 %wt. were obtained using NaBH4 or H2 as reducing agents and tested in benzene hydrogenation as a model reaction. NaBH4 reduced catalysts showed similar catalytic activity with 100 % benzene conversion after 1.5 h. Reduction with H2 resulted in a decrease of catalytic activity for all samples. High benzene conversion was achieved only in the case of 1,2-Bis(2-furylmethylene)hydrazine and ethylenediaminetetraacetic acid. It was concluded that the thermal stability of complexing agents plays a key role in activity of catalysts reduced with H2.

Effects of Halloysite Nanotubes on Mechanical and Thermal Stability of Poly(Ethylene Terephthalate)/Polycarbonate Nanocomposites

2015 ◽  
Vol 735 ◽  
pp. 8-12
Author(s):  
Nurul Ain Jamaludin ◽  
Azman Hassan ◽  
Norhayani Othman ◽  
Mohammad Jawaid
Keyword(s):  
Thermal Stability ◽  
Ethylene Terephthalate ◽  
Flexural Modulus ◽  
Halloysite Nanotubes ◽  
Mechanical And Thermal Properties ◽  
Poly Ethylene Terephthalate ◽  
Twin Screw ◽  
Poly Ethylene ◽  
The Impact ◽  
Thermal Stability Of

The objective of this study is to investigate the effect of halloysite nanotubes (HNTs) loading on mechanical and thermal properties of poly(ethylene terephthalate)/polycarbonate (PET/PC) nanocomposites. Nanocomposites containing 70PET/30PC and 2-8 phr HNTs were prepared by twin screw extruder followed by injection moulding. As the percentage of HNTs increased, the flexural modulus increased. However, the flexural strength decreased with increasing HNTs content. The impact strength also decreased when HNTs increased. Thermogravimetry analysis of PET/PC/HNTs nanocomposites showed higher thermal stability at high HNTs content. However, on further addition of HNTs up to 8 phr, thermal stability of the nanocomposites decreased due to the poor dispersion of HNTs.

scholarly journals Ruthenium-Loaded Halloysite Nanotubes as Mesocatalysts for Fischer–Tropsch Synthesis

Molecules ◽  
2020 ◽  
Vol 25 (8) ◽  
pp. 1764 ◽  
Author(s):  
Anna Stavitskaya ◽  
Kristina Mazurova ◽  
Mikhail Kotelev ◽  
Oleg Eliseev ◽  
Pavel Gushchin ◽  
...  
Keyword(s):  
Ethylenediaminetetraacetic Acid ◽  
Halloysite Nanotubes ◽  
Tropsch Synthesis ◽  
Fischer Tropsch ◽  
Fischer Tropsch Synthesis ◽  
X Ray ◽  
Ru Nanoparticles ◽  
Temperature Programmed ◽  
Major Factors ◽  
Acetone Azine

Halloysite aluminosilicate nanotubes loaded with ruthenium particles were used as reactors for Fischer–Tropsch synthesis. To load ruthenium inside clay, selective modification of the external surface with ethylenediaminetetraacetic acid, urea, or acetone azine was performed. Reduction of materials in a flow of hydrogen at 400 °C resulted in catalysts loaded with 2 wt.% of 3.5 nm Ru particles, densely packed inside the tubes. Catalysts were characterized by N2-adsorption, temperature-programmed desorption of ammonia, transmission electron microscopy, X-ray fluorescence, and X-ray diffraction analysis. We concluded that the total acidity and specific morphology of reactors were the major factors influencing activity and selectivity toward CH4, C2–4, and C5+ hydrocarbons in the Fischer–Tropsch process. Use of ethylenediaminetetraacetic acid for ruthenium binding gave a methanation catalyst with ca. 50% selectivity to methane and C2–4. Urea-modified halloysite resulted in the Ru-nanoreactors with high selectivity to valuable C5+ hydrocarbons containing few olefins and a high number of heavy fractions (α = 0.87). Modification with acetone azine gave the slightly higher CO conversion rate close to 19% and highest selectivity in C5+ products. Using a halloysite tube with a 10–20-nm lumen decreased the diffusion limitation and helped to produce high-molecular-weight hydrocarbons. The extremely small C2–C4 fraction obtained from the urea- and azine-modified sample was not reachable for non-templated Ru-nanoparticles. Dense packing of Ru nanoparticles increased the contact time of olefins and their reabsorption, producing higher amounts of C5+ hydrocarbons. Loading of Ru inside the nanoclay increased the particle stability and prevented their aggregation under reaction conditions.

Evaluation of the Impact of Fatty Acid Methyl Ester (FAME) Contamination on the Thermal Stability of Jet A

2013 ◽  
Author(s):  
Jr Morris ◽  
Shardo Robert W. ◽  
Higgins James ◽  
Cook Kim ◽  
Tanner Rhonda ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Fatty Acid ◽  
Methyl Ester ◽  
Fatty Acid Methyl Ester ◽  
Acid Methyl Ester ◽  
Acid Methyl ◽  
The Impact ◽  
Thermal Stability Of

scholarly journals Isothermal Vulcanization and Non-Isothermal Degradation Kinetics of XNBR/Epoxy/XNBR-g-Halloysite Nanotubes (HNT) Nanocomposites

Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 2872
Author(s):  
Seyed Mohamad Reza Paran ◽  
Ghasem Naderi ◽  
Elnaz Movahedifar ◽  
Maryam Jouyandeh ◽  
Krzysztof Formela ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Degradation Kinetics ◽  
Halloysite Nanotubes ◽  
Butadiene Rubber ◽  
Order Model ◽  
Scanning Calorimetry ◽  
Theoretical Methods ◽  
Vulcanization Kinetics ◽  
Kinetics Of ◽  
Thermal Stability Of

The effect of several concentrations of carboxylated nitrile butadiene rubber (XNBR) functionalized halloysite nanotubes (XHNTs) on the vulcanization and degradation kinetics of XNBR/epoxy compounds were evaluated using experimental and theoretical methods. The isothermal vulcanization kinetics were studied at various temperatures by rheometry and differential scanning calorimetry (DSC). The results obtained indicated that the nth order model could not accurately predict the curing performance. However, the autocatalytic approach can be used to estimate the vulcanization reaction mechanism of XNBR/epoxy/XHNTs nanocomposites. The kinetic parameters related to the degradation of XNBR/epoxy/XHNTs nanocomposites were also assessed using thermogravimetric analysis (TGA). TGA measurements suggested that the grafted nanotubes strongly enhanced the thermal stability of the nanocomposite.

Catalytic activity of niobium oxynitride and carbide I. Preparation, characterization and thermal stability of finely divided niobium oxynitrides

1994 ◽  
Vol 119 (2) ◽  
pp. 223-240 ◽  
Author(s):  
Hak Soo Kim ◽  
Chae Ho Shin ◽  
Guy Bugli ◽  
Monique Bureau-Tardy ◽  
Gerald Djega-Mariadassou
Keyword(s):  
Thermal Stability ◽  
Catalytic Activity ◽  
Thermal Stability Of

Characterization and Catalytic Activity of Poly(4-Vinylpyridine-Co-Divinylbenzene)-Co2+ Complex

2005 ◽  
Vol 494 ◽  
pp. 363-368 ◽  
Author(s):  
D. Lončarević ◽  
Ž. Čupić
Keyword(s):  
Catalytic Activity ◽  
Molecular Level ◽  
Supported Catalysts ◽  
Lone Pair ◽  
Polymer Support ◽  
Polymeric Complex ◽  
Reaction Conditions ◽  
Pyridine Nitrogen ◽  
Nitrogen Lone Pair ◽  
Thermal Stability Of

Poly(4-vinylpyridine-co-divinylbenzene)-Co2+ was characterized using infrared spectroscopy (IR), thermogravimetric analysis (TG-DTA), N2-physisorption and polarography. Thermal analysis suggests sufficient thermal stability of the polymer support, under reaction conditions. From polarography measurements, the Co2+ content on polymer-supported catalysts is estimated and it was proved that no significant leaching occurred during the activity tests. At the molecular level, FTIR of P4VP-DVB-Co2+ reveals that the pyridine nitrogen lone pair coordinates to the metal center in the polymeric complex. The obtained P4VP-DVB-Co2+ catalysts performed interesting catalytic activity in reaction of the cyclohexane oxidation with air, indicating that increasing Co2+ content lowers the initiation temperature and raises the decomposition of cyclohexylhydroperoxide.

scholarly journals Preparation and Characterization of Spherical Submicron CL-20 by Siphon Spray Refinement

2020 ◽  
Vol 2020 ◽  
pp. 1-9 ◽  
Author(s):  
Jiangtao Xing ◽  
Weili Wang ◽  
Wenzheng Xu ◽  
Tianle Yao ◽  
Jun Dong ◽  
...  
Keyword(s):  
Impact Sensitivity ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Crystal Forms ◽  
Refined Method ◽  
Diffraction Angle ◽  
Ultrasonic Assisted ◽  
The Impact ◽  
Thermal Stability Of

In order to improve the safety of hexanitrohexaazaisowurtzitane (CL-20), submicron CL-20 particles were prepared by a siphon ultrasonic-assisted spray refining experimental device. The samples were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), and differential scanning calorimetry (DSC), and the impact sensitivity of the samples was tested. The results show that the particle size of siphon-refined CL-20 is about 800 nm~1 μm, which is more smooth, mellow, and dense than that of CL-20 prepared by a traditional pressure-refined method. The peak diffraction angle of pressure- and siphon-refined CL-20 is basically the same as that of raw CL-20, and their crystal forms are ε type. The peak strength of pressure- and siphon-refined CL-20 decreased obviously. The apparent activation energy of pressure-refined CL-20 and siphon-refined CL-20 is 13.3 kJ/mol and 11.95 kJ/mol higher than that of raw CL-20, respectively. The thermal stability of CL-20 is improved. The activation enthalpy (ΔH#) is significantly higher than that of raw CL-20, and the characteristic drop is 70.4% and 82.7% higher than that of raw CL-20. The impact sensitivity of siphon-refined CL-20 is lower than that of pressure-refined CL-20, so the safety performance of an explosive is improved obviously.

scholarly journals Removal of tetracyclines in wastewater : accumulation and distribution of chlortetracycline in bulk water and biomass compartments in activated sludge

2021 ◽  
Author(s):  
Ruba F. Farkh
Keyword(s):  
Microbial Community ◽  
Activated Sludge ◽  
Ethylenediaminetetraacetic Acid ◽  
Divalent Cations ◽  
Bulk Water ◽  
Microbial Cells ◽  
Initial Concentration ◽  
Anoxic Conditions ◽  
Polymeric Substance ◽  
The Impact

A study was conducted to examine the removal of chlortetracycline and its distribution and accumulation in three compartments; bulk water, extracellular polymeric substance (EPS) and the microbial cells in activated sludge. Also the effect of different environmental conditions on the distribution and accumulation in the three compartments was investigated. Effluent samples collected from a municipal activated sludge treatment system were set up in bath experiments to test the distribution and accumulation of chlortetracycline under aerobic and anoxic conditions for 14 days. In addition, the impact of the activity of the microbial community on the amassing of the antibiotic in the biomass was examined. The effect of divalent cations on import and accumulation of chlortetracycline was tested. Sorption in believed to be the main removal pathway in wastewater treatment systems for tetracyclines in general and chlortetracycline in particular. In this study that notion was confirmed, and it was found that the removal via sorption under anoxic condition (43.2%) is almost double of that under aerobic conditions (27.0%). The amount of what accumulated in the cells compared to that sorbed in the EPS is twice as much in the former and triple as much in the latter. These findings suggest that changes in the structure and charge of the EPS could be the reason of higher accumulation in the polymeric substance. The impact of microbial activity on the sorption and distribution of the chlortetracycline in the three compartments showed almost a similar behaviour to that under aerobic and anoxic conditions. It was clear that the more viable the microbial community, the less the antibiotic accumulated in the [sic] both biomass compartments; the EPS and microbial cells. Biomass with inhibited respiration accrued 90% of the initial concentration; where as the active microbial community was more resistant and only 24.2% of the initial concentration accumulated within the cells. The findings suggest that the antibiotic makes its way to the cells thus bypassing the EPS, and is trapped in the EPS as it is pumped out of the cells in an energy dependent mechanism. The presence of ethylenediaminetetraacetic acid (EDTA) which is a strong chelator had no import effect. Nevertheless it did indicate that the accumulation in the EPS could be attributed to the presence of cations since there was a high negative correlation (-0.98) between the disappearance of the antibiotic from the EPS compartment and the EDTA concentration used in incubation.

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