scholarly journals Preparation of Nickel Nanocatalysts and Application to the Hydrodechlorination of 3-Chlorophenol under Liquid Phase

2021 ◽  
Vol 2021 ◽  
pp. 1-9
Author(s):  
Thanh Thien Co ◽  
Thi Kim Anh Tran ◽  
Thi Huong Ly Doan ◽  
Thi Duyen Diep
Keyword(s):  
Electron Microscopy ◽  
Atmospheric Pressure ◽  
Nickel Nanoparticles ◽  
Nickel Salt ◽  
X Ray Diffraction ◽  
N2 Adsorption ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Vanadium Phosphorus Oxides

Nickel nanoparticles were successfully synthesized via the reduction of nickel salt using ethylene glycol (EG) and sodium borohydride (NaBH4) as reducing agents. These nickel nanoparticles were then loaded on the supports as Ni-X (X = vanadium phosphorus oxides (VPO), TiO2, and ZnO) in high loading yield. The optical properties of these catalysts were characterized by UV-vis spectroscopy, the structure of Ni-X was studied by powder X-ray diffraction (PXRD), the distribution of Ni particles in X was studied by transmission electron microscopy (TEM), and the specific surface area of Ni-X was evaluated by N2 adsorption isotherm analysis at 77 K. All results corroborated the loading process. Indeed, TEM image indicated that the nickel nanoparticles size is in the range of 14 ÷ 16 nm and fully loaded into X. The activities of these catalysts were performed on the hydrodechlorination of 3-chlorophenol in the presence of sodium hydroxide as base at atmospheric pressure and at RT. The results showed that Ni-X exhibited high activities up to 98% within 90 min in the case of Ni-ZnO catalyst.

scholarly journals Microwave-assisted preparation of ZnS and ZnSe nanocrystals with different morphologies for photodegradation process of organic dyes

2019 ◽  
Author(s):  
Katarzyna Matras-Postolek ◽  
A. Zaba ◽  
S. Sovinska ◽  
D. Bogdal
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Organic Dyes ◽  
Zinc Sulphide ◽  
Conventional Heating ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy

Zinc sulphide (ZnS) and zinc selenide (ZnSe) and manganese-doped and un-doped with different morphologies from 1D do 3D microflowers were successfully fabricated in only a few minutes by solvothermal reactions under microwave irradiation. In order to compare the effect of microwave heating on the properties of obtained  nanocrystals, additionally the synthesis under conventional heating was conducted additionally in similar conditions. The obtained nanocrystals were systematically characterized in terms of structural and optical properties using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance UV-Vis spectroscopy (DR UV-Vis), Fourier-transform infrared spectroscopy (FT-IR), photoluminescence spectroscopy (PL), X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) surface area analysis. The photocatalytic activity of ZnSe, ZnS, ZnS:Mn and ZnSe:Mn nanocrystals with different morphologies was evaluated by the degradation of methyl orange (MO) and Rhodamine 6G (R6G), respectively. The results show that Mn doped NCs samples had higher coefficient of degradation of organic dyes under ultraviolet irradiation (UV).

Facile synthesis of water-soluble graphene-based composite: Non-covalently functionalized with chitosan-ionic liquid conjugation

2016 ◽  
Vol 09 (03) ◽  
pp. 1650045 ◽  
Author(s):  
Pei-Ying Li ◽  
Kai-Yu Cheng ◽  
Xiu-Cheng Zheng ◽  
Pu Liu ◽  
Xiu-Juan Xu
Keyword(s):  
Electron Microscopy ◽  
Ionic Liquid ◽  
Chemical Reduction ◽  
Water Soluble ◽  
X Ray Diffraction ◽  
Facile Synthesis ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Text Interaction

Chitosan-ionic liquid conjugation (CILC), which was prepared through the reaction of 1-(4-bromobutyl)-3-methylimidazolium bromide (BBMIB) with chitosan, was firstly used to prepare functionalized graphene composite via the chemical reduction of graphene oxide (GO). The obtained water soluble graphene-based composite was characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), ultraviolet-visible (UV–Vis) spectroscopy and so on. CILC-RGO showed excellent dispersion stability in water at the concentration of 2.0 mg/mL, which was stable for several months without any precipitate. This may be ascribed to the electrostatic attraction and [Formula: see text]–[Formula: see text] interaction between CILC and graphene.

Preparation of Al-doped ZnO Nanoparticulate Film for Optoelectronic Applications

2010 ◽  
Vol 1247 ◽  
Author(s):  
Thu V. Tran ◽  
Shinya Maenosono
Keyword(s):  
Electron Microscopy ◽  
Optical Transmittance ◽  
X Ray Diffraction ◽  
High Concentration ◽  
Polar Solvents ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Doped Zno ◽  
Optoelectronic Applications

AbstractAl-doped ZnO (AZO) nanoparticles (NPs) were synthesized by the solvothermal decomposition. The as-synthesized AZO NPs were characterized by X-ray diffraction and transmission electron microscopy. These NPs were well dispersible in non-polar solvents at high concentration to produce AZO nanoink. The AZO nanoparticulate films were prepared from AZO nanoink by spin coating technique. Thickness, surface morphology, optical transparency and conductivity of the films were characterized by surface profilometer, scanning electron microscopy, UV-Vis spectroscopy and Hall measurements. The AZO nanoparticlulate films had highly optical transmittance and well electrical conductivity, which are potential for optoelectronic applications.

The Preparation and Photocatalytic Activity of Ni-Doped ZnS Nanoparticles

2010 ◽  
Vol 148-149 ◽  
pp. 845-848 ◽  
Author(s):  
Qiao Feng Han ◽  
Guo Zhu Diao ◽  
Xiao Heng Liu ◽  
Xin Wang
Keyword(s):  
Electron Microscopy ◽  
Uv Light ◽  
Degradation Efficiency ◽  
X Ray Diffraction ◽  
Zns Nanoparticles ◽  
X Ray ◽  
Ethyl Xanthate ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Zinc Sulfide Nanoparticles

Zinc sulfide nanoparticles as undoped and doped with nickel have been prepared by the reaction of Zn(CH3COO)2 and Ni(CH3COO)2 with potassium O-ethyldithiocarbonate (ethyl xanthate, C2H5OCS2k) at 80 in N, N - dimethylformamide (DMF) solution for 24 h. The structures of the products were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM), and their optical properties were studied by UV-Vis spectroscopy. The photocatalytic experiment by degrading methyl orange in aqueous solution under UV light indicated that the degradation efficiency of Ni (6%)-doped ZnS nanoparticles increased to 75% with comparison to 43% of degradation efficiency for undoped ZnS nanoparticles.

Synthesis of Fe2+ Ion Doped ZnS Nanoparticles

2014 ◽  
Vol 879 ◽  
pp. 155-163 ◽  
Author(s):  
Rahizana Mohd Ibrahim ◽  
Markom Masturah ◽  
Huda Abdullah
Keyword(s):  
Electron Microscopy ◽  
Optical Properties ◽  
Quantum Confinement Effect ◽  
Band Gap Energy ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Co Precipitation

Nanoparticles of Zn1-xFexS ( x=0.0,0.1,0.2 and 0.3) were prepared by chemical co-precipitation method from homogenous solution of zinc and ferum salt at room temperature with controlled parameter. These nanoparticles were sterically stabilized using Sodium Hexamethaphospate (SHMP). Here, a study of the effect of Fe doping on structure, morphological and optical properties of nanoparticles was undertaken. Elemental analysis, morphological and optical properties have been investigated by Fourier-Transform-Infrared spectroscopy (FT-IR), X-Ray Fluorescence (XRF), Field Emmision Scanning Electron Microscopy (FESEM), X-ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and UV-Visible Spectroscopy. FTIR measurement confirmed the presence of SHMP in the nanoparticles structure with the FESEM images depicting considerable less agglomeration of particles with the presence of SHMP. While XRF results confirm the presence of Fe2+ ion as prepared in the experiment. The particles sizes of the nanoparticles lay in the range of 2-10 nm obtained from the TEM image were in agreement with the XRD results. The absorption edge shifted to lower wavelengths with an increase in Fe concentration shown in the UV-Vis spectroscopy. The band gap energy value was in the range of 4.95 5.15 eV. The blueshift is attributed to the quantum confinement effect.

Synthesis of Silicon Carbide Nanowires Doped with Al2O3

2007 ◽  
Vol 353-358 ◽  
pp. 2171-2174 ◽  
Author(s):  
Thanut Jintakosol ◽  
Pisith Singjai
Keyword(s):  
Electron Microscopy ◽  
Silicon Carbide ◽  
Atmospheric Pressure ◽  
Inner Core ◽  
Alumina Coating ◽  
X Ray Diffraction ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Graphite Rod

Synthesis of silicon carbide nanowires (SiC NWs) from an alumina doped silica-graphite rod is reported. The rod was gradually heated up to a growth temperature by passing current through it under constant flowing argon at atmospheric pressure. The as-grown layers, deposited on the rod surface were separated from the inner core and characterized using scanning electron microscopy, transmission electron microscopy, energy dispersive spectroscopy, selected area electron diffraction, X-ray diffraction and Raman spectroscopy. A non-uniform layer thickness of alumina coating on SiC NWs was clearly observed when the doping was increased from 1 to 2 and 3 wt.%.

scholarly journals Biosynthesis, characterisation and therapeutic applications of plant-mediated silver nanoparticles

2018 ◽  
Vol 83 (5) ◽  
pp. 515-538 ◽  
Author(s):  
Andreia Corciova ◽  
Bianca Ivanescu
Keyword(s):  
Electron Microscopy ◽  
Silver Nanoparticles ◽  
Nanoparticle Synthesis ◽  
Special Importance ◽  
X Ray Diffraction ◽  
X Ray ◽  
Stabilizing Agents ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Nanoparticles Synthesis

Nanotechnology is one of the most studied domains, and nanoparticle synthesis, especially of silver nanoparticles, has gained special importance due to their properties, biocompatibility and applications. Today, the processes of nanoparticles synthesis tend toward the development of inexpensive, simple, non-toxic and environmentally friendly methods. Thus, the use of plants in the synthesis of silver nanoparticles has attracted considerable interest because biomolecules can act as both reducing and stabilizing agents. This survey aims at discussing the conditions for obtaining silver nanoparticles using plants and their characterization by several methods, such as FTIR and UV?Vis spectroscopy, X-ray diffraction, and scanning and transmission electron microscopy. In addition, it examines some of the most common biological uses of silver nanoparticles: antibacterial, antioxidant and cytotoxic.

scholarly journals Physical Characteristics of Titania Nanofibers Synthesized by Sol-Gel and Electrospinning Techniques

2010 ◽  
Vol 5 (1) ◽  
pp. 155892501000500 ◽  
Author(s):  
Soo-Jin Park ◽  
Yong C. Kang ◽  
Ju Y. Park ◽  
Ed A. Evans ◽  
Rex D. Ramsier ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Average Diameter ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Ceramic Nanofibers ◽  
Titania Nanofibers

Titania nanofibers were successfully synthesized by sol-gel coating of electrospun polymer nanofibers followed by calcining to form either the pure anatase or rutile phases. Characterization of these materials was carried out using scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance Fourier transform infrared spectroscopy (DRIFTS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and UV-vis spectroscopy techniques. The average diameter of these ceramic nanofibers was observed to be around 200 nm for both the rutile and anatase forms. The valence band structure and optical absorption thresholds differ, however, indicating that nanofibrous mats of titania can be selectively developed for different applications in catalysis and photochemistry.

scholarly journals The Effect of AgInS2, SnS, CuS2, Bi2S3 Quantum Dots on the Surface Properties and Photocatalytic Activity of QDs-Sensitized TiO2 Composite

Catalysts ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 403 ◽  
Author(s):  
Anna Malankowska ◽  
Daria Kulesza ◽  
Jakub Sowik ◽  
Onur Cavdar ◽  
Tomasz Klimczuk ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Quantum Dots ◽  
Photocatalytic Activity ◽  
Surface Properties ◽  
Toluene Degradation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Hot Injection

The effect of type (AgInS2, SnS, CuS2, Bi2S3) and amount (5, 10, 15 wt%) of quantum dots (QDs) on the surface properties and photocatalytic activity of QDs-sensitized TiO2 composite, was investigated. AgInS2, SnS, CuS2, Bi2S3 QDs were obtained by hot-injection, sonochemical, microwave, and hot-injection method, respectively. To characterize of as-prepared samples high-resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), UV-Vis spectroscopy and photoluminescence (PL) emission spectroscopy were applied. The size of AgInS2, SnS, CuS2, Bi2S3 QDs were 12; 2–6; 2–3, and 1–2 nm, respectively. The QDs and QDs-sensitized TiO2 composites obtained have been tested in toluene degradation under LEDs light irradiation (λmax = 415 nm and λmax = 375 nm). For pristine QDs the efficiency of toluene degradation increased in the order of AgInS2 < Bi2S3 < CuS < SnS under 375 nm and AgInS2 < CuS < Bi2S3 < SnS under 415 nm. In the presence of TiO2/SnS QDs_15% composite, 91% of toluene was degraded after 1 h of irradiation, and this efficiency was about 12 higher than that for pristine QDs under 375 nm. Generally, building the TiO2/AgInS2 and TiO2/SnS exhibited higher photoactivity under 375 nm than the pristine TiO2 and QDs which suggests a synergistic effect between QDs and TiO2 matrix.

scholarly journals Microwave assisted hydrothermal synthesize of ZnO nanorods and their characterization

2012 ◽  
Vol 05 ◽  
pp. 72-78
Author(s):  
NADI SHOJAEE ◽  
TOURADJ EBADZADEH ◽  
ALIREZA AGHAEI
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solution ◽  
Zno Nanorods ◽  
Heating Time ◽  
Zinc Nitrate ◽  
X Ray Diffraction ◽  
X Ray ◽  
Domestic Microwave Oven ◽  
Transmission Electron ◽  
Vis Spectroscopy

In present study ZnO nanorods were synthesized in an aqueous solution using a domestic microwave oven for irradiation. The nanorods have been grown on substrates immersed in an aqueous solution which contains zinc nitrate and hexamethylenetetramine as precursors. Eventually, effect of some parameters such as precursor's concentration and heating time on growth mechanism was characterized. The product phase was detected using X-ray diffraction (XRD). Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) exhibited the resultant structure is uniform and single crystalline. Finally Uv-Vis spectroscopy was used to measure the nanorod's band gap.

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