Synthesis and Characterization of Silica-Alumina Supported Ca and Ni Catalyst for Deoxygenation of Vegetable Oil into Diesel

2016 ◽  
Vol 840 ◽  
pp. 353-358 ◽  
Author(s):  
Nurul Aiskin Mijan ◽  
Hwei Voon Lee ◽  
Abdulkareem Ghassan Alsultan ◽  
Yun Hin Taufiq-Yap
Keyword(s):  
Vegetable Oil ◽  
Catalyst Activity ◽  
High Surface ◽  
High Surface Area ◽  
Ni Catalyst ◽  
High Porosity ◽  
X Ray ◽  
Mesoporous Support ◽  
Silica Alumina ◽  
Temperature Programme Desorption

Developing an environmentally friendly and high-quality of fuel from vegetable oil (triglycerides) have attracted a great attention among the researches. Deoxygenation reaction using Ca-based catalyst is a potentially promising element for removing an oxygen species from organic compounds and converting the molecule to hydrocarbon. Addition of transition metal in the catalysis synthesis studies not only could enhance the properties of the catalyst but also could tune the selectivity toward desired product. Cooperation of mesoporous support such as silica alumina (SA) exhibit unique and excellent properties (high surface area, high porosity) which simultaneously could increase the catalyst activity. In the present studies, a set of bifunctional acid-base supported on the highly mesoporous SA doped with Ca and Ni were synthesized. The Ca (NO)3 and Ni (NO)3 were impregnated on the mesoporous SA support and were calcined at 500 °C for 2 h in order to activate the synthesized catalyst. The physicochemical properties of the catalyst were characterized by X-Ray fluorescence spectroscopy (XRF), X-Ray diffraction spectroscopy (XRD), temperature programme desorption carbon dioxide (TPD-CO2) and temperature programme desorption ammonia (TPD-NH3) and scanning electron microscopy (SEM).

scholarly journals Fractal Structure in Silica and Composites Aerogels

Gels ◽  
2020 ◽  
Vol 7 (1) ◽  
pp. 1
Author(s):  
Thierry Woignier ◽  
Juan Primera ◽  
Adil Alaoui ◽  
Philippe Dieudonne ◽  
Laurent Duffours ◽  
...  
Keyword(s):  
Fractal Structure ◽  
High Surface ◽  
High Surface Area ◽  
Silica Aerogels ◽  
High Porosity ◽  
Material Density ◽  
X Ray ◽  
Synthesis Conditions ◽  
Fractal Characteristics ◽  
Synthesis Procedure

Silica aerogels are known to be materials with exceptional characteristics, such as ultra-low density, high surface area, high porosity, high adsorption, and low-thermal conductivity. In addition, these unique properties are mainly related to their specific processing. Depending on the aerogel synthesis procedure, the aerogels texture can be tailored with meso and/or macroporosity. Fractal geometry has been observed and used to describe silica aerogels at nanoscales in certain conditions. In this review paper, we describe the fractal structure of silica aerogels that can develop depending on the synthesis conditions. X-ray and neutron scattering measurements allow to show that silica aerogels can exhibit a fractal structure over one or even more than two orders of magnitude in length. The fractal dimension does not depend directly on the material density but can vary with the synthesis conditions. It ranges typically between 1.6 and 2.4. The effect of the introduction of silica particles or of further thermal treatment or compression of the silica aerogels on their microstructure and their fractal characteristics is also resumed.

scholarly journals Preparation of modified paints with nano-structured additives and its potential applications

2020 ◽  
Vol 10 ◽  
pp. 184798042090918
Author(s):  
Ricardo Solano ◽  
David Patiño-Ruiz ◽  
Adriana Herrera
Keyword(s):  
Electron Microscopy ◽  
Zno Nanoparticles ◽  
Uv Light ◽  
High Surface ◽  
High Surface Area ◽  
Antibacterial Properties ◽  
Normal Function ◽  
High Porosity ◽  
X Ray ◽  
Self Cleaning

Recently, an increase in the production of intelligent nanomaterials has been reported for the application of solid surface coating. These nanomaterials provide a wide number of functionalities such as anticorrosive, antibacterial, and self-cleaning properties. Hence, titanium dioxide (TiO2) and zinc oxide (ZnO) nanoparticles were synthesized using a green chemistry approach. These nanoparticles were fully characterized by scanning electron microscopy, energy-dispersive X-ray, high-resolution transmission electron microscopy, X-ray diffraction, ultraviolet (UV)–visible spectroscopy, Brunauer–Emmett–Teller test, and nitrogen adsorption–desorption isotherm. Then, a commercial enamel-type paint was modified by using different concentrations (2, 3.5, and 5 w/v%) of nanoparticles. These nanofilled paints were then brushed onto the surface of different types of materials such as carbon steel sheets, wood sheets, and aluminum disks. Anticorrosive, self-cleaning, and antibacterial properties of the nanofilled paints were evaluated, with the aim to determine the capability for this application. According to the characterization results, TiO2 and ZnO nanoparticles exhibited similar physicochemical properties compared to those synthesized using traditional methods. The anticorrosion results revealed that nanofilled paints provide a barrier using low concentrations of nanoparticles, due to the decrease of agglomerates on the surface avoiding the presence of high porosity. In the case of self-cleaning, a proposed mechanism of degradation demonstrated that the presence of both nanoparticles in the paint provided high degradation of methylene blue due to the high surface area offered by the nanoparticles. On the other hand, antibacterial activity under UV light was observed only for ZnO nanoparticles, which may be related to the diffusion of nanoparticles into the cell membrane of the bacteria, affecting the normal function. These results showed to be promising for the modification of paints with TiO2 and ZnO nanoparticles, and the application on solid surfaces for the construction, and even in textile fields.

scholarly journals Non-Thermal Plasma-Modified Ru-Sn-Ti Catalyst for Chlorinated Volatile Organic Compound Degradation

Catalysts ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1456
Author(s):  
Yujie Fu ◽  
You Zhang ◽  
Qi Xin ◽  
Zhong Zheng ◽  
Yu Zhang ◽  
...  
Keyword(s):  
Plasma Treatment ◽  
Photoelectron Spectroscopy ◽  
High Surface ◽  
High Surface Area ◽  
Surface Oxidation ◽  
Treatment Method ◽  
X Ray ◽  
Chlorinated Volatile Organic Compounds ◽  
Volatile Organic ◽  
Doped Titania

Chlorinated volatile organic compounds (CVOCs) are vital environmental concerns due to their low biodegradability and long-term persistence. Catalytic combustion technology is one of the more commonly used technologies for the treatment of CVOCs. Catalysts with high low-temperature activity, superior selectivity of non-toxic products, and resistance to chlorine poisoning are desirable. Here we adopted a plasma treatment method to synthesize a tin-doped titania loaded with ruthenium dioxide (RuO2) catalyst, possessing enhanced activity (T90%, the temperature at which 90% of dichloromethane (DCM) is decomposed, is 262 °C) compared to the catalyst prepared by the conventional calcination method. As revealed by transmission electron microscopy, X-ray diffraction, N2 adsorption, X-ray photoelectron spectroscopy, and hydrogen temperature-programmed reduction, the high surface area of the tin-doped titania catalyst and the enhanced dispersion and surface oxidation of RuO2 induced by plasma treatment were found to be the main factors determining excellent catalytic activities.

scholarly journals Attached β-cyclodextrin/γ-(2,3-epoxypropoxy) propyl trimethoxysilane to graphene oxide and its application in copper removal

2017 ◽  
Vol 75 (10) ◽  
pp. 2403-2411 ◽  
Author(s):  
Zongxue Yu ◽  
Qi Chen ◽  
Liang Lv ◽  
Yang Pan ◽  
Guangyong Zeng ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
High Surface ◽  
High Surface Area ◽  
Esterification Reaction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Cavity Structure ◽  
Optimum Ph ◽  
Exchange Adsorption ◽  
Langmuir Isotherm Model

The environmental applications of graphene oxide and β-cyclodextrin (β-CD) have attracted great attention since their first discovery. Novel nanocomposites were successfully prepared by using an esterification reaction between β-cyclodextrin/γ-(2,3-epoxypropoxy) propyl trimethoxysilane grafted graphene oxide (β-CD/GPTMS/GO). The β-CD/GPTMS/GO nanocomposites were used to remove the Cu2+ from aqueous solutions. The characteristics of β-CD/GPTMS/GO were detected by scanning electron microscopy (SEM), Fourier transform infrared, X-ray diffraction (XRD), thermogravimetric analysis (TG) and energy dispersive X-ray (EDX). The dispersibility of graphene oxide was excellent due to the addition of β-CD. The adsorption isotherms data obtained at the optimum pH 7 were fitted by Langmuir isotherm model. The excellent adsorption properties of β-CD/GPTMS/GO for Cu2+ ions could be attributed to the apolar cavity structure of β-CD, the high surface area and abundant functional groups on the surface of GO. The adsorption patterns of β-CD/GPTMS/GO were electrostatic attraction, formation of host-guest inclusion complexes and the ion exchange adsorption. The efficient adsorption of β-CD/GPTMS/GO for Cu2+ ions suggested that these novel nanocomposites may be ideal candidates for removing other cation pollutants from waste water.

Highly stable metal-organic framework UiO-66-NH2 for high-performance triboelectric nanogenerators

2021 ◽  
Author(s):  
Yong-Mei Wang ◽  
Xinxin Zhang ◽  
Dingyi Yang ◽  
Liting Wu ◽  
Jiaojiao Zhang ◽  
...  
Keyword(s):  
High Performance ◽  
Metal Organic Framework ◽  
High Surface ◽  
High Surface Area ◽  
Triboelectric Nanogenerator ◽  
High Porosity ◽  
Chemically Modified ◽  
Metal Organic ◽  
Triboelectric Nanogenerators ◽  
Organic Framework

Abstract The high porosity, controllable size, high surface area, and chemical versatility of a metal-organic framework (MOF) enable it a good material for a triboelectric nanogenerator (TENG), and some MOFs have been incorporated in the fabrication of TENGs. However, the understanding of effects of MOFs on the energy conversion of a TENG is still lacking, which inhibits the improvement of the performance of MOF-based TENGs. Here, UiO-66-NH2 MOFs were found to significantly increase the power of a TENG and the mechanism was carefully examined. The electron-withdrawing ability of Zr-based UiO-66-family MOFs was enhanced by designing the amino functionalized 1,4-terephthalic acid (1,4-BDC) as ligand. The chemically modified UiO-66-NH2 was found to increase the surface roughness and surface potential of a composite film with MOFs embedded in polydimethylsiloxane (PDMS) matrix. Thus the total charges due to the contact electrification increased significantly. The composite-based TENG was found to be very durable and its output voltage and current were 4 times and 60 times higher than that of a PDMS-based TENG. This work revealed an effective strategy to design MOFs with excellent electron-withdrawing abilities for high-performance TENGs.

Facile Synthesis of Unique Bismuth Vanadate Nano-Knitted Hollow Cage and its Application in Environmental Remediation

2019 ◽  
Vol 74 (3) ◽  
pp. 259-263 ◽  
Author(s):  
M. Shamshi Hassan
Keyword(s):  
Environmental Remediation ◽  
Dye Degradation ◽  
High Surface ◽  
High Surface Area ◽  
Bismuth Vanadate ◽  
Bandgap Energy ◽  
Blue Dye ◽  
X Ray ◽  
Photodegradation Efficiency ◽  
Hollow Nanostructure

AbstractHierarchical bismuth vanadate (BiVO4) nano-knitted hollow cages have been synthesized by simple hydrothermal method and characterized by scanning electron microscopy, x-ray diffraction, energy-dispersive x-ray spectrometer, Fourier transform infrared, UV-Vis, and Raman. The photodegradation efficiency of BiVO4 nanocage for universally used methylene blue dye. The BiVO4 hollow nanostructure demonstrated better photocatalytic competence in dye degradation as compared to the commercial TiO2 powders (P25). The excellent dye degradation can be certified to the high crystallisation of monoclinic BiVO4 and hollow nanostructure, which leads to high surface area and small bandgap energy of 2.44 eV.

scholarly journals Operando SAXS Study of a Pt/C Fuel Cell Catalyst with an X-ray Laboratory Source

2021 ◽  
Author(s):  
Johanna Schröder ◽  
Jonathan Quinson ◽  
Jacob J. K. Kirkensgaard ◽  
Matthias Arenz
Keyword(s):  
Fuel Cell ◽  
Background Subtraction ◽  
Stress Test ◽  
High Surface ◽  
High Surface Area ◽  
Carbon Support ◽  
Grazing Incidence ◽  
Saxs Data ◽  
X Ray ◽  
Fuel Cell Catalysts

Small angle X-ray scattering (SAXS) is a powerful technique to investigate the degradation of catalyst materials. Ideally such investigations are performed <i>operando</i>, i.e., during a catalytic reaction. An example of <i>operando </i>measurements is to observe the degradation of fuel cell catalysts during an accelerated stress test (AST). Fuel cell catalysts consist of Pt or Pt alloy nanoparticles (NPs) supported on a high surface area carbon. A key challenge of operando SAXS measurements is a proper background subtraction of the carbon support to extract the information of the size distribution of the Pt NPs as a function of the AST treatment. Typically, such operando studies require the use of synchrotron facilities. The background measurement can then be performed by anomalous SAXS (aSAXS) or in a grazing incidence con-figuration. In this work we present a proof-of-concept study demonstrating the use of a laboratory X-ray diffractometer for <i>operando </i>SAXS. Data acquisition of <i>operando </i>SAXS with a laboratory X-ray diffractometer is desirable due to the general challenging and limited accessibility of synchrotron facilities. They become even more crucial under the ongoing and foreseen restrictions related to the COVID-19 pandemic. Although, it is not the aim to completely replace synchrotron-based studies, it is shown that the background subtraction can be achieved by a simple experimental consideration in the setup that can ultimately facilitate <i>operando </i>SAXS measurements at a synchrotron facility. <br>

scholarly journals Organomineral nanocomposite carbon burial during Oceanic Anoxic Event 2

2014 ◽  
Vol 11 (5) ◽  
pp. 6815-6844
Author(s):  
S. C. Löhr ◽  
M. J. Kennedy
Keyword(s):  
Surface Area ◽  
High Surface ◽  
High Surface Area ◽  
Mineral Surfaces ◽  
Mineral Surface ◽  
X Ray ◽  
Oceanic Anoxic Event ◽  
Carbon Burial ◽  
Anoxic Events ◽  
Mineral Surface Area

Abstract. Organic carbon (OC) enrichment in sediments deposited during Oceanic Anoxic Events (OAEs) is commonly attributed to elevated productivity and marine anoxia. We find that OC enrichment in the late Cenomanian aged OAE2 at Demerara Rise was controlled by co-occurrence of anoxic bottom-water, sufficient productivity to saturate available mineral surfaces and variable deposition of high surface area detrital smectite clay. Redox indicators show consistently oxygen-depleted conditions, while a strong correlation between OC concentration and sediment mineral surface area (R2=0.92) occurs across a range of TOC values from 9–33%. X-ray diffraction data indicates intercalation of OC in smectite interlayers while electron, synchrotron infrared and X-ray microscopy show an intimate association between clay minerals and OC, consistent with preservation of OC as organomineral nanocomposites and aggregates rather than discrete, μm-scale pelagic detritus. Since the consistent ratio between TOC and mineral surface area suggests that excess OC relative to surface area is lost, we propose that it is the varying supply of smectite that best explains variable organic enrichment against a backdrop of continuous anoxia, which is conducive to generally high TOC during OAE2 at Demerara Rise. Smectitic clays are unique in their ability to form stable organomineral nanocomposites and aggregates that preserve organic matter, and are common weathering products of continental volcanic deposits. An increased flux of smectite coinciding with high carbon burial is consistent with evidence for widespread volcanism during OAE2, so that organomineral carbon burial may represent a potential feedback to volcanic degassing of CO2.

scholarly journals Synthesis of Fe2SiO4-Fe7Co3 Nanocomposite Dispersed in the Mesoporous SBA-15: Application as Magnetically Separable Adsorbent

Molecules ◽  
2020 ◽  
Vol 25 (4) ◽  
pp. 1016 ◽  
Author(s):  
Monickarla da Silva ◽  
Felipe Barbosa ◽  
Marco Morales Torre ◽  
Jhonny Villarroel-Rocha ◽  
Karim Sapag ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
High Surface ◽  
High Surface Area ◽  
Dye Adsorption ◽  
Santa Barbara ◽  
Mesoporous Support ◽  
Magnetically Separable ◽  
Temperature Programmed ◽  
Positive Effect ◽  
Isolated Species

The mixture containing alloy and oxide with iron-based phases has shown interesting properties compared to the isolated species and the synergy between the phases has shown positive effect on dye adsorption. This paper describes the synthesis of Fe2SiO4-Fe7Co3-based nanocomposite dispersed in Santa Barbara Amorphous (SBA)-15 and its application in dye adsorption followed by magnetic separation. Thus, it was studied the variation of reduction temperature and amount of hydrogen used in synthesis and the effect of these parameters on the physicochemical properties of the iron and cobalt based oxide/alloy mixture, as well as the methylene blue adsorption capacity. The XRD and Mössbauer results, along with the temperature-programmed reduction (TPR) profiles, confirmed the formation of Fe2SiO4-Fe7Co3-based nanocomposites. Low-angle XRD, N2 isotherms, and TEM images show the formation of the SBA-15 based mesoporous support with a high surface area (640 m2/g). Adsorption tests confirmed that the material reduced at 700 °C using 2% of H2 presented the highest adsorption capacity (49 mg/g). The nanocomposites can be easily separated from the dispersion by applying an external magnetic field. The interaction between the dye and the nanocomposite occurs mainly by π-π interactions and the mixture of the Fe2SiO4 and Fe7Co3 leads to a synergistic effect, which favor the adsorption.

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