Preparation and Evaluation of a Photo-Fenton Heterogeneous Catalyst: Spinel-Typed ZnFe2O4

2012 ◽  
Vol 550-553 ◽  
pp. 329-335 ◽  
Author(s):  
Ping Li ◽  
Huan Yan Xu ◽  
Xue Li ◽  
Wei Chao Liu ◽  
Yan Li

In this study, spinel-typed ZnFe2O4 was synthesized through Sol-Gel method, using fresh egg white as a complexing agent, and characterized by XRD and SEM. Then, the synthesized sample was used as the photo-Fenton heterogeneous catalyst for the discoloration of methyl orange (MO) in solution. The XRD results show that the synthesized sample was pure, only with the spinel structure, when the volume ratio of the fresh egg white/ferric nitrate/zinc nitrate was 2:2:1. And the lowest sintered temperature to obtain the single-phase ZnFe2O4 was 500°C. The SEM results reveal that the ZnFe2O4 crystalline grains presented irregular shapes and desultorily aggregated together, with a average diameter of 150-250nm. The experimental results show that MO could be efficiently discolored in photo-Fenton system of ZnFe2O4 and H2O2, under UV irradiation. MO discoloration ratio increased as H2O2 dosage increasing. The optimum dosage of ZnFe2O4 was 1g/L in this study. With the MO initial concentration increasing, MO discoloration ratio decreased. The ZnFe2O4 sample obtained at 500°C exhibited the optimum MO discoloration ratio. Finally, the mechanism for MO discoloration in the photo-Fenton system was discussed.

2020 ◽  
Vol 34 (33) ◽  
pp. 2050379
Author(s):  
Zhuo Zuo ◽  
Aimin Sun ◽  
Lichao Yu ◽  
Nanzhaxi Suo ◽  
Wei Zhang ◽  
...  

In this paper, nickel nitrate, copper nitrate, cobalt nitrate, ferric nitrate were used as raw materials, citric acid was used as a complexing agent, and chromium nitrate was used as a modifier to synthesize [Formula: see text] by sol–gel method. The sample was characterized. X-ray diffraction (XRD) data on the sample showed that the particle size of the sample was 52.14–54.88 nm. The lattice constant varied from 8.3569 Å to 8.3758 Å. The data of Fourier infrared showed that the sample did not change with the structure of the doped sample of Cr ion and remained as the spinel type. It can be seen by SEM that the sample is irregularly spherical. Due to the doping of chromium ions, it appears agglomerated. Analysis of the elements of the sample by EDAX revealed that the sample contained Ni, Cu, Co, Fe, O and a peak corresponding to the Cr element was found in the sample having crion content of 0.025, 0.050, 0.075 and 0.100. The magnetic properties of the samples were characterized using VSM. The data are processed to obtain magnetic parameters such as saturation magnetization and coercivity.


2018 ◽  
Vol 9 (1) ◽  
pp. 133-139
Author(s):  
Waleed S. Mohammed ◽  
Ahmed H. El-Shazly ◽  
Marwa F. Elkady ◽  
Masahiro Ohshima

Introduction: The utilization of biodiesel as an alternative fuel is turning out to be progressively famous these days because of worldwide energy deficiency. The enthusiasm for utilizing Jatropha as a non-edible oil feedstock is quickly developing. The performance of the base catalyzed methanolysis reaction could be improved by a continuous process through a microreactor in view of the high mass transfer coefficient of this technique. Materials & Methods: Nanozirconium tungstovanadate, which was synthetized using sol-gel preparation method, was utilized in a complementary step for biodiesel production process. The prepared material has an average diameter of 0.066 &µm. Results: First, the NaOH catalyzed methanolysis of Jatropha oil was investigated in a continuous microreactor, and the efficient mixing over different mixers and its impact on the biodiesel yield were studied under varied conditions. Second, the effect of adding the nanocatalyst as a second stage was investigated. Conclusion: The maximum percentage of produced methyl esters from Jatropha oil was 98.1% using a methanol/Jatropha oil molar ratio of 11 within 94 s using 1% NaOH at 60 &°C. The same maximum conversion ratio was recorded with the nanocatalyst via only 0.3% NaOH.


Planta Medica ◽  
2021 ◽  
Author(s):  
Sandra Alves de Sousa Garcia ◽  
Priscila Bianca Rodrigues da Rocha ◽  
Bruno dos Santos Souza ◽  
Andressa Tuane Santana Paz ◽  
Ana Luiza Caetano Negris ◽  
...  

AbstractPunicalagin, the principal ellagitannin of Lafoensia pacari leaves, has proven antioxidant activity, and standardized extracts of L. pacari can be topically used for skin aging management. We hypothesized that Pluronic nanomicelles or vesicles could solubilize sufficiently large amounts of the standardized extracts of L. pacari and provide chemical stability to punicalagin. The standardized extracts of L. pacari were obtained with an optimized extraction procedure, and the antioxidant activity was characterized. Formulations containing Pluronic at 25% and 35% were obtained with or without Span 80. They were characterized by average diameter, polydispersity index, punicalagin content, physicochemical stability, and rheology. A release and skin permeation study was carried out in vertical diffusion cells. The extraction procedure allowed quantifying high punicalagin content (i.e., 141.61 ± 3.87 mg/g). The standardized extracts of L. pacari showed antioxidant activity for all evaluated methods. Pluronic at 25 and Pluronic at 35 with standardized extracts of L. pacari showed an average diameter of about 25 nm. The addition of Span 80 significantly increased the mean diameter by 15-fold (p < 0.05), indicating the spontaneous formation of vesicles. Pluronic formulations significantly protected punicalagin from chemical degradation (p < 0.05). Pluronic at 25 formulations presented as free-flowing liquid-like systems, while Pluronic at 35 resulted in an increase of about 44-fold in |ƞ*|. The addition of Span 80 significantly reduced the Pluronic sol-gel transition temperature (p < 0.05), indicating the formation of vesicles. Formulations with Span 80 significantly enhanced punicalagin skin permeation compared to formulations without Span 80 (p < 0.05). Formulations with Span 80 were demonstrated to be the most promising formulations, as they allowed significant permeation of punicalagin (about 80 to 315 µg/cm2), which has been shown to have antioxidant activity.


Nanophotonics ◽  
2020 ◽  
Vol 9 (15) ◽  
pp. 4497-4503
Author(s):  
Liying Zhang ◽  
Xiangqian Xiu ◽  
Yuewen Li ◽  
Yuxia Zhu ◽  
Xuemei Hua ◽  
...  

AbstractVertically aligned nanowire arrays, with high surface-to-volume ratio and efficient light-trapping absorption, have attracted much attention for photoelectric devices. In this paper, vertical β-Ga2O3 nanowire arrays with an average diameter/height of 110/450 nm have been fabricated by the inductively coupled plasma etching technique. Then a metal-semiconductor-metal structured solar-blind photodetector (PD) has been fabricated by depositing interdigital Ti/Au electrodes on the nanowire arrays. The fabricated β-Ga2O3 nanowire PD exhibits ∼10 times higher photocurrent and responsivity than the corresponding film PD. Moreover, it also possesses a high photocurrent to dark current ratio (Ilight/Idark) of ∼104 and a ultraviolet/visible rejection ratio (R260 nm/R400 nm) of 3.5 × 103 along with millisecond-level photoresponse times.


2010 ◽  
Vol 658 ◽  
pp. 29-32 ◽  
Author(s):  
Kanit Soongprasit ◽  
Duangdao Aht-Ong ◽  
Viboon Sricharoenchaikul ◽  
Duangduen Atong

. La1-xCexCoO3 (x=0, 0.2, and 0.4) perovskite-type mixed oxides using polyvinyl alcohol (PVA) as complexing agent at two molar ratio of metal ion to PVA (1:1 and 1:2) were successfully prepared by sol-gel process. The precursor included lanthanum (II) nitrate hexahydrate, cerium (II) nitrate hexahydrate, and cobalt (II) nitrate hexahydrate where polyvinyl alcohol was added as complexing agent. The suitable condition of Cerium (Ce) substitution and PVA molar ratio were established for further application in hydrocarbon conversion to high value added products. TGA thermogram of as-prepared precursor showed that PVA absolutely decomposed at temperature higher than 500°C. XRD patterns of calcined catalyst showed both LaCoO3 rhombohedral and CeO2 cubic structures that confirmed the formation of mixed crystal structure. Nevertheless, Co3O4 slightly appeared with low peak intensity which came from the oxidation reaction of as-prepared catalyst during calcinations. XRD showed that PVA did not effect to crystal structure of synthesized catalyst. Higher PVA content added in the precursor cause the reduction of crystal growth of catalyst in calcinations step. In contrast, morphology of catalyst is directly related with PVA content such that the spongy and sheet-like structure were formed with increasing PVA content which prevented the agglomeration of particles. The results showed that PVA content play an important role in morphology of perovskite-type mixed oxide catalysts but did not affected to their crystal structures.


2011 ◽  
Vol 295-297 ◽  
pp. 813-816 ◽  
Author(s):  
Li Liu

Silicon dioxide-based nanocomposites offer large loading capacity for various doping chemicals or molecular complexes, high surface to volume ratio and customizable surface chemistry for the creation and development of novel sensors and devices [1-2]. When compared with other sol-gel materials, xerogels represent a class of nanocomposites that are relatively easy to fabricate but with unique thermal, acoustic, optical and mechanical properties for rapid sensor or device prototyping development [3-4]. Xerogels in solids are formed by controlled evaporation of the liquid in the hydro-gel. Their porosity and morphology depend largely on the temperature, gel chemical compositions and pH in the fabrication process. When impregnated with fluorescent compounds in their nanosize cavities, the doped xerogels exhibit strong and stable fluorescence properties that are useful for the developing of ion-exchange sensors and optical devices. However, the use of these fluorescently doped xerogels in forensic applications was still largely unexplored.


2000 ◽  
Vol 613 ◽  
Author(s):  
Sun Hyuk Bae ◽  
Jae-Hyun So ◽  
Seung-Man Yang ◽  
Do Hyun Kim

ABSTRACTSilica slurry used as abrasives in wafer polishing process is made by dispersing silica particles in an alkali solution. Since commercially available colloidal or fumed silica particles need some modifications to be directly used as abrasive slurry due to their small sizes, irregular shapes or broad size distribution, we have prepared silica abrasives by particle growth of fumed silica or colloidal silica as seeds by sol-gel method. Silica slurries prepared by this step-wise growth from commercial seeds were tested using one-armed polisher for the comparison with commercial slurries and showed the performance comparable to commercial slurries. Microstructures of polishing slurries were investigated using transmission electron microscopy and ARES rheometer. From the result, stability of the slurry was found to be more important than the primary particle sizes for the polishing performance.


2021 ◽  
Vol 317 ◽  
pp. 447-453
Author(s):  
Noor Hidayah Aniza Zakaria ◽  
Nafisah Osman

NiO nanoparticle was synthesized by a sol-gel method with three different pH values namely pH=1, 7 and 11, and then calcined at temperature of 450 ᵒC. The influence of different pH values on the physical properties of NiO nanoparticles were investigated by a particle size analyzer (PSA), field emission scanning electron microscope (FESEM) and X-ray diffractometer (XRD). Structural analysis confirmed that a cubic structure of NiO nanoparticle was obtained without any secondary phase for NiO powders prepared with pH=1, while the peak of secondary phase (Ni) appeared for NiO powders prepared with pH= 7 and 11. Morphological observation showed that the NiO nanoparticles prepared with pH=7 and 11 tend to form more agglomerates compared to one prepared with pH=1. The average diameter of NiO nanoparticles with pH 1, 7 and 11 were approximately in the range of 19-26 nm, 21-28 nm, and 24-30 nm, respectively. NiO powder that was synthesized with pH=1 was further used to prepare composite anode of NiO Nps-BaCe0.54Zr0.36Y0.1O2.95 (BCZY) powder. Unfortunately a composite of NiO Nps-BaCeO3-BaZrO3 was obtained instead of BCZY and governed by agglomerates with size in the range of 70-300 nm.


2021 ◽  
Author(s):  
Yanchun Zhang ◽  
Aimin Sun ◽  
Zhaxi Suonan

Abstract Different complexing agents were used to prepare Ni-Mg-Zn ferrite with the composition formula Ni0.2Mg0.2Zn0.6Fe2O4 via sol-gel method, which included citric acid, oxalic acid, egg white and EDTA. The Ni0.2Mg0.2Zn0.6Fe2O4 ferrite with no complexing agent was also prepared as a comparison. The chemical phases of samples were analyzed by the X-ray diffraction (XRD), which indicated that samples had spinel phase structure. The lattice constants of samples are in the range of 8.3980 ~ 8.4089 Å. The composition and structure were further studied by fourier transform infrared spectroscopy (FTIR). There were two typical characteristic bands related to the stretching vibrations of spinel ferrite in FTIR spectra. Scanning electron microscope (SEM) micrographs and transmission electron microscope (TEM) images showed that the particles have the shape of spherical cube. Energy dispersive spectrometer (EDS) analyzed the elements and ingredients of samples, which included Ni, Mg, Zn, Fe and O. X-ray photoelectron spectroscopy (XPS) is used to examine further the elemental composition and chemical state of sample prepared with EDTA as complexing agent. The optical properties of samples were investigated by photoluminescence spectra and UV-Vis spectroscopy. Vibrating sample magnetometer (VSM) was used to characterize magnetic properties, hysteresis loops revealed the ferrimagnetism behavior of prepared samples.


2014 ◽  
Vol 1024 ◽  
pp. 83-86 ◽  
Author(s):  
Mohamad Sahban Alnarabiji ◽  
Noorhana Yahya ◽  
Sharifa Bee Abd Hamid ◽  
Khairun Azizi Azizli ◽  
Afza Shafie ◽  
...  

Synthesising zinc oxide nanoparticles to get certain specific characteristics to be applied in Enhanced oil recovery (EOR) is still challenging to date. In this work, zinc oxide (ZnO) nanoparticles were synthesised using the sol-gel method by dissolving zinc nitrate hexahydrate in nitric acid. The ZnO crystal and particles morphology and structure were determined using X-ray Diffractometer (XRD) and Field Emission Scanning Electron Microscope (FESEM). In this study, a microwave oven was used for annealing ZnO without insulating a sample in any casket. The results show that 30 and 40 minutes of annealing and stirring for 1 hour influenced the morphology and size of zinc oxide particles in nanoscale. These parameters could be tailored to generate a range of nanoparticle morphology (agglomerated nanoparticles in a corn-like morphology), a crystal size with the mean size of 70.5 and 74.9 nm and a main growth at the peak [10. EOR experiment were conducted by dispersing 0.10 wt% ZnO NPs in distilled water to form a ZnO nanofluid. Then the fluid was injected into the medium in the 3rd stage of the oil recovery to present EOR stage. It was found that ZnO nanofluid has the ability to extract 8% of the original oil in place (OOIP).


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