scholarly journals Enhancement of Efficiency of Pd/Al2O3Catalysts in Selective Hydrogenation of Sec-Butylbenzene by Modification with H2SO4 or H2WO4

Metals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 281
Author(s):  
Leonid M. Kustov ◽  
Andrei L. Tarasov ◽  
Alexander L. Kustov ◽  
Olga P. Tkachenko

Hydrogenation of bulky aromatic hydrocarbons is an important problem to be solved in order to improve the quality of fuels. Pd-containing catalysts modified by strong acids have been prepared and studied by diffuse-reflectance IR spectroscopy, and the catalytic activity of the materials has been determined. In studying the selective liquid-phase hydrogenation of sec-butylbenzene as a model substrate, it was shown that modification of Pd/Al2O3 catalysts with acid additives (H2SO4 or H2WO4) results in a significant increase in the hydrogenation activity and selectivity. IR spectroscopy of adsorbed CO and d3-acetonitrile revealed that larger palladium metal particles are formed on the Pd-H2SO4(H2WO4)/Al2O3 catalysts, with ionic states of palladium being present even in the samples reduced in H2.

1980 ◽  
Vol 45 (8) ◽  
pp. 2219-2223 ◽  
Author(s):  
Marie Jakoubková ◽  
Martin Čapka

Kinetics of homogenous hydrogenation of 1-heptene catalysed by rhodium(I) complexes prepared in situ from μ,μ'-dichloro-bis(cyclooctenerhodium) and phosphines of the type RP(C6H5)2 (R = -CH3, -(CH2)nSi(CH3)3; n = 1-4) have been studied. The substitution of the ligands by the trimethylsilyl group was found to increase significantly the catalytic activity of the complexes. The results are discussed in relation to the electron density on the phosphorus atom determined by 31P NMR spectroscopy and to its proton acceptor ability determined by IR spectroscopy.


Author(s):  
B. G. Abdulov ◽  
A. A. Hasanov

The purification process of polycyclic aromatic hydrocarbons was carried out by extraction of diesel fraction from the primary oil refining using the effect of magnetic field. A mixture of N-methylpyrrolidone with sulfuric acid was used as an extractant. The content of aromatic hydrocarbons in the diesel fraction decreased by 39.8% under normal conditions and by 50.8% under the influence of magnetic field after extraction. The samples were investigated by infrared (IR) spectroscopy method before and after extraction. Vibartional modes corresponding to different atomic bonds have been observed. Deodorization of diesel was determined by interpreting obtained modes.


2012 ◽  
Vol 512-515 ◽  
pp. 2381-2385
Author(s):  
Xue Mei Zhang ◽  
Feng Xing Niu

We have successfully prepared a novel passivation Ni/HY catalyst by the technologies of macerate-precipitatio.The catalysts are comprised of two contents: HY as carrier, Ni as active component,and we put it into the process of preparating aromatic amines.The nature of the catalysts was discussed based on the characterization results of BET , IR , SEM , XRD , TEM ,TPD , XPS and TPR . The catalytic hydrogenation technology for 2,4-dinitrobenzene in liquid phase can be an attractive and elegant routine for production of 2,4-tolylenediamine. The catalytic activity is evaluated at 2.2 MPa, 90 °C, 750r/min, solvent with reaction materials mass ratio of 60, catalyst with reaction materials mass ratio of 0.1. In the catalytic test, The experimental results over the catalyst showed that 2,4-dinitrobenzene and 2,4-tolylenediamine conversion and selective of 99.88% and 99.16% were obtained respectively.It is found that the catalyst is highly dispersion, stable, and reusable. No obvious deactivation of the catalyst was observed after repeated using twelve times.


1982 ◽  
Vol 36 (2) ◽  
pp. 155-157 ◽  
Author(s):  
D. B. Chase ◽  
R. L. Amey ◽  
W. G. Holtje

Diffuse reflectance FT-IR spectroscopy is used to obtain infrared spectra of paints directly on paper panels. The binder contribution to the spectrum can be effectively eliminated by spectral subtraction and the spectra of photodecomposition products are obtained. Comparison with reference spectra allows the determination of the photodecomposition mechanism.


2017 ◽  
Author(s):  
◽  
Sharista Raghunath

The presence of dyes in effluent poses various environmental as well as health hazards for many organisms. Although various remediation strategies have been implemented to reduce their effect, dyes still manage to infiltrate into the environment and hence new strategies are required to address some of the problems. This study investigated the innovation of two cationic water-soluble polymers viz., Proline-Epichlorohydrin-Ethylenediamine Polymer (PEP) and Thiazolidine-Epichlorohydrin-Ethylenediamine Polymer (TEP) that were used to remediate selected synthetic dyes from synthetic effluent by adsorption and dye reduction. Both polymers were synthesized using monomers of a secondary amine, epichlorohydrin and ethylenediamine and were subsequently characterized and modified and their remediation potential studied. In the first study, PEP was synthesized and characterized by 1H-NMR Spectroscopy, FT-IR Spectroscopy, dynamic light scattering, and thermogravimetric analysis (TGA). Thereafter PEP was modified with bentonite clay, by simple mixing of the reactants, to form a Proline-Epichlorohydrin-Ethylenediamine Polymer-bentonite composite (PRO-BEN); it was characterized by FT-IR Spectroscopy, scanning electron microscopy (SEM)/ energy dispersive X-ray spectroscopy (EDX), dynamic light scattering (DLS), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). Adsorption studies were then undertaken with a synthetic effluent containing three textile dyes, viz., Reactive Blue 222 (RB 222), Reactive Red 195 (RR 195) and Reactive Yellow (RY 145). Various conditions were investigated including pH of the solution, temperature, sodium chloride concentration, initial dye concentration and the dosage of adsorbent used. The experimental data for all dyes followed a Langmuir isotherm. The adsorption process was found to be pseudo-second order. According to the thermodynamic parameters, the adsorption of the dyes was classified as physisorption and the reaction was spontaneous and exothermic. The data were also compared using studies with alumina as an adsorbent. Results showed that PRO-BEN exhibited better absorptivity and desorption than alumina making its use a better recyclable remediation strategy for the removal of organic dyes in wastewater treatment plants. In the second study, TEP was synthesized and then characterized by FT-IR Spectroscopy, 1H-NMR Spectroscopy, TGA and DLS. Thereafter, TEP was used to prepare TEP capped gold nanoparticles (TEP-AuNPs). Herein, two methods were investigated: the Turkevich method and an adaptation of the Turkevich method using bagasse extract. The TEP-AuNPs was characterized by FT-IR Spectroscopy, SEM, EDX, DLS and TEM. Thereafter the reduction of each of Allura Red, Congo Red and Methylene Blue was investigated with the TEP-AuNPs for its catalytic activity toward dye reduction. This study showed that the batch of AuNPs prepared by the Turkevich method had higher rates of dye reduction compared with AuNPs prepared using bagasse extract. Also the quantity of TEP used as capping agent greatly influenced the size, shape and surface charge of the nanoparticles as well as their catalytic performance: the Vroman effect explained this behavior of the TEP-AuNPs. It was finally concluded that whilst PRO-BEN, in the first study, showed excellent dye remediation properties, the second study on TEP-AuNPs showed good catalytic activity for the reduction of selected dyes, however, it was more effective at lower polymer concentration. Finally, both materials displayed good potential for the clean-up of selected synthetic dyes from synthetic effluents.


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