RESUMEN
[This corrects the article DOI: 10.1021/acsomega.9b00485.].
RESUMEN
Addressed herein, thiourea functionalized graphene oxide-based PtRu nanocatalysts (PtRu@T/GO) has been synthesized and characterized by several techniques and performed for methanol oxidation reactions as novel catalysts. In this study, graphene oxide (GO) was functionalized with thiourea (T/GO) in order to obtain monothiol functionalized graphene and increase the stability and activity of the nanocatalysts. Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), TEM (transmission electron microscopy) and high-resolution transmission electron microscopy (HR-TEM) were used for characterization of the prepared nanocatalysts. The results obtained from these techniques showed that the prepared nanocatalysts were in a highly crystalline form, well dispersed on T/GO, very small in size and colloidally stable. The average size of the synthesized nanocatalysts determined by TEM analysis was found to be 3.86 ± 0.59 nm. With HR-TEM analysis, the atomic lattice fringes of the nanocatalysts were calculated to be 0.23 nm. After the full characterization of the prepared nanocatalysts, they were tried for the methanol oxidation reaction (MOR) and it was observed that 97.3% of the initial performance was maintained even after 1000 cycles while exhibiting great catalytic activity and stability with the help of T/GO. Thus, the arranged nanocatalysts displayed great heterogeneous catalyst characteristics for the methanol oxidation response.
RESUMEN
The intense demand for alternative energy has led to efforts to find highly efficient and stable electrocatalysts for the methanol oxidation reaction. For this purpose, herein, graphene oxide-based platinum-cobalt nanoparticles (Pt100-xCox@GO NPs) were synthesized in different ratios and the synthesized nanoparticles were used directly as an efficient electrocatalyst for methanol oxidation reaction (MOR). The characterizations for the determination of particle size and surface composition of nanoparticles were performed by transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The structure of the catalysts was detected as face-centered cubic and the dispersion of them on graphene oxide was homogenous (distributed narrowly (4.01 ± 0.51 nm)). Cyclic voltammetry (CV) and chronoamperometry (CA) was utilized for testing electrocatalytic activities of all prepared NPs for the methanol oxidation reaction. It was detected that the newly produced NPs were more active and stable than commercially existing Pt(0)/Co nanomaterial in methanol electro-oxidation in acidic media.
RESUMEN
Herein, we report a facile method for the preparation of polypyrrole-multi walled carbon nanotube hybrid material including Pt nanoparticles (Pt@PPy-MWCNT NPs) and the use in methylamine borane (MeAB) for hydrolysis reaction at mild conditions. The prepared catalyst of Pt@PPy-MWCNT NPs was characterized by some advanced analytical methods. The catalytic experiments showed the Pt@PPy-MWCNT NPs can catalyze MeAB in aquatic solution with high catalytical performance at mild conditions. The reaction rate of catalytic hydrolysis with Pt@PPy-MWCNT NPs was found to be -d[CH3NH2BH3]/dt = + d[H2]/3dt = kobs[Pt@PPy-MWCNT]1.19 [MeAB]0.88. The TOF value for the hydrolysis of MeAB catalyzed with Pt@PPy-MWCNT NPs was detected to be 10234.2 1/h (170.57 1/min) which is very high compared with TOF values found for other catalysts. Enthalpy, entropy and activation energy for the hydrolysis of MeAB were calculated to be 31.57 kJ mol-1, -119.97 J mol-1 K and 34.27 kJ mol-1, respectively.
RESUMEN
Several metal nanoparticle based catalysts have been synthesized for catalyzing the hydrogen production process by hydrolysis of methylamine-borane (MeAB). However, there was only one study that catalyzes the producing of hydrogen via the methanolysis of MeAB, and it was carried out by our research group. For this reason, in this work, a new catalyst system entitled by single-walled carbon nanotube (SWCNT) supported bimetallic platinum-ruthenium nanoparticles were developed and called as PtRu@SWCNT. These NPs were characterized by several techniques (XRD, XPS, Raman, and TEM), and they were performed for the methanolysis of MeAB with high catalytic activity. The prepared PtRu@SWCNT NPs were also tested in the methanolysis of MeAB at different parameters including different temperatures, catalyst and substrate concentrations, and reusability performance. Experimental results revealed that the new PtRu@SWCNT NPs had excellent catalytic activity and reusability for removing of hydrogen from the methanolysis of MeAB at ambient conditions. According to the obtained data, the turnover frequency is 136.25 mole H2/mole PtRu × min, and the activation energy (Ea) is 17.29 kJ/mole. More than 99% of conversion was observed at room temperature.
RESUMEN
Herein, we have described uniformly dispersed palladium-nickel nanoparticles furnished on graphene oxide (GO-supported PdNi nanoparticles) as a powerful heterogeneous nanocatalyst for the promotion of Knoevenagel reaction between malononitrile and aromatic aldehydes under mild reaction conditions. The successful characterization of PdNi nanoparticles on the GO surface was shown by X-ray diffraction, X-ray photoelectron spectroscopy, high-resolution transmission electron microscopy (HR-TEM), and TEM. GO-supported PdNi nanoparticles, which are used as highly efficient, stable, and durable catalysts, were used for the first time for the Knoevenagel condensation reaction. The data obtained here showed that the GO-supported PdNi nanocatalyst had a unique catalytic activity and demonstrated that it could be reused five times without a significant decrease in the catalytic performance. The use of this nanocatalyst results in a very short reaction time under mild reaction conditions, high recyclability, excellent catalytic activity, and a straightforward work-up procedure for Knoevenagel condensation of malononitrile and aromatic aldehydes.
RESUMEN
Herein, multiwalled carbon nanotube-based Fe3O4 nano-adsorbents (Fe3O4@MWCNT) were synthesized by ultrasonic reduction method. The synthesized nano-adsorbent (Fe3O4@MWCNT) exhibited efficient sonocatalytic activity to remove Maxilon Blue 5G, a textile dye, and present in a cationic form, in aqueous solution under ultrasonic irradiation. The magnetic nano-adsorbent particles were characterized by high-resolution transmission electron microscopy (HR-TEM), transmission electron microscopy (TEM), Raman spectroscopy and X-ray diffraction (XRD). Some important parameters such as nano-adsorbent dosage, solution pH, initial dye and H2O2 concentration, reaction time, ultrasonic power and temperature were tested to determine the optimum conditions for the elimination of Maxilon Blue 5G dye. The reusability results showed that Fe3O4@MWCNT nano-adsorbent has a decrease of about 32.15% in the removal efficiency of Maxilon Blue 5G under ultrasonic irradiation after six times reuse. Additionally, in order to reveal the sufficient kinetic explanation, various experiments were performed at different temperatures and testing three kinetic models like the pseudo-first-order, pseudo-second-order and intraparticle diffusion for removal adsorption process of Maxilon Blue 5G using Fe3O4@MWCNT nano-adsorbent. The experimental kinetic results revealed that the adsorption process of Maxilon Blue 5G in the aquatic mediums using sono-Fenton method was found to be compatible with the intraparticle diffusion. Using kinetic models and studies, some activation parameters like enthalpy, entropy and Gibbs free energy for the adsorption process were calculated. The activation parameters indicated that Fe3O4@MWCNT nano-adsorbent could be used as an effective adsorbent for the removal of Maxilon Blue 5G as a textile dye and the adsorption process of Maxilon Blue 5G with Fe3O4@MWCNT nano-adsorbent is spontaneous.
RESUMEN
In this study, a facile ex situ synthesis of a polyaniline-multiwalled carbon nanotube-based Pt nanocatalyst (Pt@PANI-MWCNT) with an average particle size of 3.18⯱â¯0.12â¯nm was performed successfully. The obtained Pt@PANI-MWCNT nanocatalysts were isolated from the solution medium by centrifugation and then were characterized by spectroscopy and microscopy methods. The characterization studies showed that the prepared Pt nanoparticles were formed on PANI-MWCNT surface, and H2 evolution was obtained by the dehydrogenation of hydrazine-borane in water as a model reaction under room temperature conditions, with the help of the synthesized nanocatalyst. It was observed that the Pt@PANI-MWCNT nanocatalyst had a very high catalytic activity for the hydrolytic dehydrogenation of hydrazine-borane and generated 2.95â¯mol of H2 for 1â¯mol of hydrazine-borane. The initial turn-over frequency (TOFinitial) value of the prepared nanocatalyst for the model reaction at room temperature conditions was found to be 168.5â¯min-1. The calculations for the kinetics of the hydrolytic dehydrogenation reaction showed that the hydrazine-borane catalytic reaction kinetics are first order, with respect to the catalyst concentration; several activation parameters, such as entropy (ΔS#, appâ¯=â¯-72.11⯱â¯3â¯J/mol K), enthalpy (ΔH#, appâ¯=â¯43.5⯱â¯2â¯kJ/mol) and activation energy (Ea,appâ¯=â¯45.5⯱â¯2â¯kJ/mol), of the catalytic reaction with the Pt@PANI-MWCNT nanocatalyst were calculated using these kinetic data.
RESUMEN
In the present study, highly effective and reusable monodisperse ruthenium-nickel (Ru-Ni) nanomaterials supported on poly(N-vinyl-2-pyrrolidone) (Ru-Ni@PVP) were synthesized (3.51⯱â¯0.38â¯nm) by a facile sodium-hydroxide-assisted reduction method; Ru and Ni reduction in PVP solution was accomplished. The prepared nanocomposites were characterized by TEM, HRTEM, XRD, and XPS and performed as a catalyst for dehydrocoupling of dimethylamine-borane (DMAB). It was found that Ru-Ni nanomaterials are one of the most active catalysts at low concentrations and temperature for dehydrocoupling of DMAB. This catalyst with its turnover frequency of 458.57â¯h-1 exhibits one of the best results among all the catalysts prepared in the literature for dehydrocoupling of DMAB. Significantly low Ea value (36.52⯱â¯3â¯kJâ¯mol-1) was also found for dehydrocoupling of DMAB.