SBA-15 Supported Bimetallic Catalysts for Enhancement Isomers Production During n-Heptane Decomposition

2014 ◽  
Vol 12 (1) ◽  
pp. 345-354 ◽  
Author(s):  
Talib M. Albayati ◽  
Aidan M. Doyle

Abstract Santa Barbara Amorphous (SBA)-15 supported 1% (Pt–Ni), 1% (Pt–Co) and 1% (Ni–Co) bimetallic catalysts in a heterogeneous reaction for enhancement hydroisomerization and hydrocracking production during reforming or decomposition of n-heptane. The structural and textural features of the nanoporous silicas, both with and without encapsulated nanoparticles, were characterized using small-angle X-ray diffraction, scanning electron microscopy, EDAX, nitrogen adsorption–desorption porosimetry (Brunauer–Emmett–Teller) surface area analysis, Fourier-transform infrared spectroscopy and transmission electron microscopy. The catalytic performance was evaluated at 250–400°C under atmospheric pressure in a plug-flow reactor in a catalyst testing rig under tightly controlled conditions of temperature, reactant flow rate and pressure. The species leaving the reactor were analysed by Gas Chromatography. The results show that 1% (Pt–Ni)/SBA-15, 1% (Pt–Co)/SBA-15 and 1% (Ni–Co)/SBA-15 had a high activity for conversion of n-heptane (around 85%). The selectivity of isomerization is not high, so further studies have to be carried out in the future.

Catalysts ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 363
Author(s):  
Jieun Kim ◽  
La-Hee Park ◽  
Jeong-Myeong Ha ◽  
Eun Duck Park

The oxidative coupling of methane (OCM) is operated at high temperatures and is a highly exothermic reaction; thus, hotspots form on the catalyst surface during reaction unless the produced heat is removed. It is crucial to control the heat formed because surface hotspots can degrade catalytic performance. Herein, we report the preparation of Mn2O3-Na2WO4/SiC catalysts using SiC, which has high thermal conductivity and good stability at high temperatures, and the catalyst was applied to the OCM. Two Mn2O3-Na2WO4/SiC catalysts were prepared by wet-impregnation on SiC supports having different particle sizes. For comparison, the Mn2O3-Na2WO4/SiO2 catalyst was also prepared by the same method. The catalysts were analyzed by nitrogen adsorption–desorption, X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. The transformation of SiC into α-cristobalite was observed for the Mn2O3-Na2WO4/SiC catalysts. Because SiC was completely converted into α-cristobalite for the nano-sized SiC-supported Mn2O3-Na2WO4 catalyst, the catalytic performance for the OCM reaction of Mn2O3-Na2WO4/n-SiC was similar to that of Mn2O3-Na2WO4/SiO2. However, only the surface layer of SiC was transformed into α-cristobalite for the micro-sized SiC (m-SiC) in Mn2O3-Na2WO4/m-SiC, resulting in a SiC@α-cristobalite core–shell structure. The Mn2O3-Na2WO4/m-SiC showed higher methane conversion and C2+ yield at 800 and 850 °C than Mn2O3-Na2WO4/SiO2.


NANO ◽  
2013 ◽  
Vol 08 (05) ◽  
pp. 1350050
Author(s):  
MIN GUAN ◽  
HAI-PENG BI ◽  
ZUYUAN WANG ◽  
SHAOHUA BU ◽  
LING HUANG ◽  
...  

Mesoporous silicas SBA-15 are modified with β-Cyclodextrins (β-CD) by simple grafting method. β-CD functionalized SBA-15 was characterized by Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), powder X-ray diffraction (PXRD), nitrogen adsorption–desorption measurements, thermogravimetric analysis (TGA) and X-ray photoelectron spectroscopy (XPS). Furthermore, the applicability of it is investigated through studying the adsorption properties of clenbuterol. It showed better adsorption capacities of clenbuterol than pure SBA-15. β-CD functionalized SBA-15 material has the potential applications in the treatment of clenbuterol contamination in food and environment science.


2009 ◽  
Vol 7 (2) ◽  
pp. 259-266 ◽  
Author(s):  
Vendula Houšková ◽  
Václav Štengl ◽  
Snejana Bakardjieva ◽  
Nataliya Murafa ◽  
Václav Tyrpekl

AbstractNanocrystalline titania particles doped with ruthenium oxide have been prepared by the homogenous hydrolysis of TiOSO4 in aqueous solutions in the presence of urea. The synthesized particles were characterized by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), High Resolution Transmission Electron Microscopy (HRTEM), Selected Area Electron Diffraction (SAED) and Nitrogen adsorption-desorption was used for surface area (BET) and porosity determination (BJH). The photocatalytic activity of the Ru-doped titania samples were determined by photocatalytic decomposition of Orange II dye in an aqueous slurry during irradiation at 365 nm and 400 nm wavelengths.


NANO ◽  
2019 ◽  
Vol 14 (04) ◽  
pp. 1950046
Author(s):  
Tong Il Kim ◽  
Hak Sung Yun ◽  
Yung Jon ◽  
Gwang Bok Han ◽  
Sung Il Chae ◽  
...  

In this work, flower-like [Formula: see text]-AlOOH and [Formula: see text]-Al2O3 nanoarchitectures with excellent surface and mesoporous properties were successfully synthesized in ionic liquid-assisted hydrothermal reaction system. The as-prepared suprastructures were characterized by several techniques, such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and nitrogen adsorption/desorption measurement. The formation mechanism of flower-like [Formula: see text]-AlOOH mesoporous crystallites by ionic liquid-assisted hydrothermal process was proposed and discussed. Flower-like [Formula: see text]-Al2O3 nanostructures were obtained by calcining the as-prepared [Formula: see text]-AlOOH at 600∘C for 2[Formula: see text]h, preserving the same morphology.


2012 ◽  
Vol 626 ◽  
pp. 173-177 ◽  
Author(s):  
M. Abdus Salam ◽  
Ye Lwin ◽  
Suriati Sufian

nanostructured hydrotalcite-like compounds that contain nickel, cobalt and aluminum have been synthesized by conventional coprecipitation method without using any surfactants or templating agents. The structure and morphology of the coprecipitated nanohydrotalcites and its derived mixed oxides were characterized by powder X-ray diffraction (XRD), Fourier-transformed Infrared (FTIR) spectroscopy, field-emission scanning electron microscopy (FESEM), high resolution transmission electron microscopy (HRTEM), and nitrogen adsorption-desorption techniques. The results show that the synthesized materials exhibited micro-meso-pore networks. The cobalt-rich calcined hydrotalcites are generally amorphous, having a coral-like morphology whereas nickel-rich hydrotalcites show hexagonal plate-like morphology. The presence of nickel in mixed oxides catalyzed the reduction of Co-Al-O spinels. The Fast Fourier Transform (FFT) analysis of HRTEM revealed the inter planner distances of the crystal of hydrotalcite.


2011 ◽  
Vol 233-235 ◽  
pp. 2011-2014 ◽  
Author(s):  
Xiu Cheng Zheng ◽  
Wen Hao Ye ◽  
Zheng Lin ◽  
Bing Jie Liu ◽  
Xiao Juan Shi ◽  
...  

Ti-SBA-15 mesoporous materials were directly synthesized via a hydrothermal process and characterized by using nitrogen adsorption-desorption measurements, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, diffuse reflectance ultraviolet-visible spectroscopy, and infrared ray spectroscopy. The effect of synthesis temperatures on the structure and catalytic efficiency in epoxidation of cyclohexene was discussed in details. The results showed that the optimal temperature was 100 °C under the reaction conditions.


Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 490
Author(s):  
Rudaviro Garidzirai ◽  
Phillimon Modisha ◽  
Innocent Shuro ◽  
Jacobus Visagie ◽  
Pieter van Helden ◽  
...  

The effects of Mg and Zn dopants on the catalytic performance of Pt/Al2O3 catalyst were investigated for dehydrogenation of perhydrodibenzyltoluene (H18-DBT) as a liquid organic hydrogen carrier. Al2O3 supports were modified with Mg and Zn to produce Mg-Al2O3 and Zn-Al2O3 with a target loading of 3.8 wt.% for dopants. The modified supports were impregnated with chloroplatinic acid solution to produce the catalysts Pt/Al2O3, Pt/Mg-Al2O3 and Pt/Zn-Al2O3 of 0.5 wt.% Pt loading. Thereafter, the catalysts were characterised using inductively coupled plasma- optical emission spectrometry, scanning electron microscopy-energy dispersive X-ray spectroscopy, hydrogen temperature-programmed reduction, carbon-monoxide pulse chemisorption, ammonia temperature-programmed desorption, X-ray diffraction and transmission electron microscopy. The dehydrogenation experiments were performed using a horizontal plug flow reactor system and the catalyst time-on-stream was 22 h. Pt/Mg-Al2O3 showed the highest average hydrogen flowrate of 29 nL/h, while an average of 27 nL/h was obtained for both Pt/Al2O3 and Pt/Zn-Al2O3. This has resulted in a hydrogen yield of 80% for Pt/Mg-Al2O3, 71% for Pt/Zn-Al2O3 and 73% for Pt/Al2O3. In addition, the conversion of H18-DBT ranges from 99% to 92%, Pt 97–90% and 96–90% for Pt/Mg-Al2O3, Pt/Zn-Al2O3 and Pt/Al2O3, respectively. Following the latter catalyst order, the selectivity to dibenzyltoluene (H0-DBT) ranges from 78% to 57%, 75–51% and 71–45%. Therefore, Pt/Mg-Al2O3 showed improved catalytic performance towards dehydrogenation of H18-DBT.


Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1712
Author(s):  
Appusamy Muthukrishnaraj ◽  
Salma Ahmed Al-Zahrani ◽  
Ahmed Al Otaibi ◽  
Semmedu Selvaraj Kalaivani ◽  
Ayyar Manikandan ◽  
...  

Towards the utilization of Cu2O nanomaterial for the degradation of industrial dye pollutants such as methylene blue and methyl orange, the graphene-incorporated Cu2O nanocomposites (GCC) were developed via a precipitation method. Using Hummers method, the grapheme oxide (GO) was initially synthesized. The varying weight percentages (1–4 wt %) of GO was incorporated along with the precipitation of Cu2O catalyst. Various characterization techniques such as Fourier-transform infra-red (FT-IR), X-ray diffraction (XRD), UV–visible diffused reflectance (UV-DRS), Raman spectroscopy, thermo gravimetric analysis (TGA), energy-dispersive X-ray analysis (EDX), and electro chemical impedance (EIS) were followed for characterization. The cabbage-like morphology of the developed Cu2O and its composites were ascertained from field-emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HR-TEM). In addition, the growth mechanism was also proposed. The results infer that 2 wt % GO-incorporated Cu2O composites shows the highest value of degradation efficiency (97.9% and 96.1%) for MB and MO at 160 and 220 min, respectively. Further, its catalytic performance over visible region (red shift) was also enhanced to an appreciable extent, when compared with that of other samples.


2018 ◽  
Vol 96 (4) ◽  
pp. 394-403 ◽  
Author(s):  
Wei Long ◽  
Pingle Liu ◽  
Yang Lv ◽  
Wei Xiong ◽  
Fang Hao ◽  
...  

Silica-supported copper catalysts were prepared by different methods, and Cu/SiO2 prepared by the urea-assisted gel method was modified with co-catalyst platinum to obtain Cu-Pt/SiO2 bimetallic catalysts. The prepared catalysts were characterized by nitrogen adsorption–desorption, XRD, TEM, hydrogen chemisorption, ammonia gas chemisorption, and X-ray photoelectron spectroscopy. The characterization results show that the modification of platinum is helpful to the reduction and dispersion of copper species, which increase the hydrogen uptake quantity and metal surface area. The 30%Cu–3.0%Pt/SiO2-6 presents the best catalytic performance in liquid-phase diethyl oxalate hydrogenation; it gives 77.32% conversion of diethyl oxalate and 94.37% selectivity to the main products under 473 K and 3.0 MPa for 4 h. A possible reaction route was also proposed.


2010 ◽  
Vol 93-94 ◽  
pp. 22-26 ◽  
Author(s):  
Surachai Artkla ◽  
Won Yong Choi ◽  
Jatuporn Wittayakun

This work compared properties and catalytic performance of two hybrid photocatalysts, TiO2/RH-MCM-41 and TiO2/TEOS-MCM-41 prepared by loading nanoparticles of TiO2 (10 wt.%) on MCM-41 synthesized with rice husk silica and tetraethyl orthosilicate respectively. The supports and catalysts were characterized by X-ray diffraction, N2 adsorption-desorption, transmission electron microscopy and zeta potential. The photocatalytic activities of the TiO2/RH-MCM-41 and TiO2/TEOS-MCM-41 for the degradation of tetramethylammonium (TMA) in aqueous slurry were similar with a complete conversion after irradiation time of 90 min at pH 7.


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