scholarly journals Degradation of Phenol by Photocatalysis Using TiO2/Montmorillonite Composites Under UV Light

2021 ◽  
Author(s):  
Huijuan Li ◽  
Yeting Yao ◽  
Xiaoyan Yang ◽  
Xusheng Zhou ◽  
Ran Lei ◽  
...  
Keyword(s):  
High Performance ◽  
Ph Value ◽  
Uv Light ◽  
Irradiation Time ◽  
Phenol Degradation ◽  
Influential Factors ◽  
X Ray Diffraction ◽  
Solution Ph ◽  
Transmission Electron ◽  
Average Size

Abstract Composites of Titanium (IV) oxide combined with montmorillonite (MMT) with various TiO2/MMT were prepared for photocatalysis application. The prepared samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), and diffuse reflectance UV–visible spectroscopy. The main influential factors such as the TiO2/MMT dose, calcined temperature and pH value of the solution were studied. The main intermediates of phenol degradation were determined by High Performance Liquid Chromatography (HPLC). The results showed that the average size of TiO2 nanoparticles was decreased from 22.51 nm to 10.66 nm through the immobilization on MMT. The components in the interlayer domain were replaced by titanium pillars, and the pillaring reaction proceeded in the interlayer domain, and the basic skeleton of MMT was unchanged, and also TiO2 was dispersed on the surface of the MMT. When the initial concentration of phenol is 10 mg/L, the phenol solution pH is 6 and the UV light irradiation time is 240 min, the phenol degradation rate of 30%TiO2/MMT composite is 89.8%, which is better than MMT (11.5%) and pure TiO2 (58.8%). It shows that TiO2 loaded on MMT improves its photocatalytic activity. The phenol reaction process detected by HPLC showed that it had undergone through hydroquinone and benzoquinone, and finally converted into maleic acid and carbon dioxide and small molecules. The possible photocatalysis mechanism is presented.

Preparation and Characterization of CdSe Nanoparticles Synthesized Using the Ultrasonic Irradiation

2007 ◽  
Vol 124-126 ◽  
pp. 1229-1232 ◽  
Author(s):  
Myoung Seok Sung ◽  
Yoon Bok Lee ◽  
Yong Jin Kim ◽  
Yang Do Kim
Keyword(s):  
Ultrasonic Irradiation ◽  
Photoelectron Spectroscopy ◽  
Irradiation Time ◽  
Xrd Analysis ◽  
Cdse Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Surface Emission ◽  
Transmission Electron ◽  
Average Size

Cadmium selenide(CdSe) nanoparticles were prepared in the aqueous solution containing isopropyl alcohol by the ultrasonic irradiation at room temperature. The cadmium chloride (CdCl2) and sodium selenosulfate (Na2SeSO3) were used as the cadmium and selenium source, respectively. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), UV-Vis absorption spectra and PL spectra were used to characterize the CdSe nanoparticles. XRD analysis revealed the formation of cubic structure CdSe. TEM images showed aggregated CdSe nanoparticles with the size of nanometer scale. Average size of CdSe nanoparticles were about 3.9, 5.0 and 5.1nm with sonication time of 6, 30 and 40 minutes, respectively. The surface emission became less intensive and shifted to red with increasing irradiation time. This paper presents the effects of ultrasonic on the formation of CdSe nanoparticles and its characteristics.

scholarly journals Synthesis and characterization of gold nanoparticles on titanium dioxide for the catalytic photodegradation of 2,4-dichlorophenoxyacetic acid

2018 ◽  
Vol 16 (5) ◽  
Author(s):  
E. Romero Torres ◽  
M. Gutiérrez Arzaluz ◽  
V Mugica Alvarez ◽  
L. González Reyes ◽  
M. Torres Rodríguez ◽  
...  
Keyword(s):  
Gold Nanoparticles ◽  
Titanium Dioxide ◽  
Uv Light ◽  
Anatase Phase ◽  
Precipitation Method ◽  
Dichlorophenoxyacetic Acid ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Average Size ◽  
2,4 Dichlorophenoxyacetic Acid

The photocatalytic degradation of 2,4-dichlorophenoxyacetic acid (2,4-D) using a Au/TiO2 catalyst and ultraviolet (UV) light energy source (9 mW/cm2) discussed. Gold nanoparticles were synthesized by controlled urea reduction and deposited on titanium dioxide (TiO2) by the deposition-precipitation method. The average size of the nanoparticles was 6-8 nm. X-ray diffraction (XRD) characterization confirmed that TiO2 was present in the anatase phase, whereas the presence and particle size of gold were determined by transmission electron microscopy (TEM). The results of the degradation showed that the activity of TiO2 was improved when Au nanoparticles were present on the surface. The reactions were performed at atmospheric pressure and room temperature.

Preparation and Characterization of Magnetite Nanoparticles

2014 ◽  
Vol 618 ◽  
pp. 24-27 ◽  
Author(s):  
Fu Yan Zhao ◽  
Ya Ling Li ◽  
Lu Hai Li
Keyword(s):  
Surface Area ◽  
Magnetite Nanoparticles ◽  
High Performance ◽  
Catalytic Performance ◽  
Ammonium Bromide ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Particles Size Distribution ◽  
Magnetite Particles ◽  
Average Size

The preparation of magnetite nanoparticles with controlled size has attracted of scientific and technological broad attention. Spherical magnetite nanoparticles in the size range from 8nm to 22 nm were synthesized by coprecipiation method using hexadecyl trimethyl ammonium bromide (CTAB) as dispersant. Magnetite nanoparticles have good dispersibility and uniform particles size distribution. The properties were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), automated surface area and pore size analyzer, vibrating sample magnetometer (VSM) and the catalytic performance was measured using high performance liquid chromatography (HPLC). The saturation magnetization is 13.785emu/g, and the coercive force of the sample is 23.738G, the average size of the particles is 13.6 nm, specific surface area is 19.318 m2/g and phenol conversion is up to 99.5%. These results indicate the synthesized magnetite particles have good performance.

Anatase TiO2 Nano-Particles Preparation with Neutralization Hydrolysis Technique and Photocatalytic Performance

2010 ◽  
Vol 113-116 ◽  
pp. 1639-1643
Author(s):  
Li Lin ◽  
Cun Xi Lei ◽  
Ji Cheng Zhou
Keyword(s):  
Tio2 Nanoparticles ◽  
Ph Value ◽  
Uv Light ◽  
Particle Diameter ◽  
Nano Particles ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Excellent Activity ◽  
Key Factor ◽  
Precursor Composition

A neutralization hydrolysis route has been used to synthesize titanium oxide nanoparticles. Transmission electron microscopy(TEM) and X-ray diffraction(XRD) characteri- zation results showed the TiO2 nanoparticles were single anatase phases when calcined at 600°C-800°C for 2h. The particle diameter ranged from 15 to 30nm. The pH value was key factor for precursor composition. When pH value 2-4, the H2TiO3 precursor with low agglomeration was obtained. As-prepared anatase TiO2 nanoparticles, during photodegradation of methylic orange under UV-light irradiation(λ=254nm), exhibited excellent activity, more than 95.5% methylic orange was degraded in 1h.

scholarly journals Size Control of Synthesized Silver Nanoparticles by Simultaneous Chemical Reduction and Laser Fragmentation in Origanum majorana Extract: Antibacterial Application

Materials ◽  
2021 ◽  
Vol 14 (9) ◽  
pp. 2326
Author(s):  
Entesar Ali Ganash ◽  
Reem Mohammad Altuwirqi
Keyword(s):  
Silver Nanoparticles ◽  
Irradiation Time ◽  
Chemical Reduction ◽  
Size Control ◽  
Reduction Process ◽  
Laser Wavelength ◽  
X Ray Diffraction ◽  
Ag Nps ◽  
Transmission Electron ◽  
Origanum Majorana

In this work, silver nanoparticles (Ag NPs) were synthesized using a chemical reduction approach and a pulsed laser fragmentation in liquid (PLFL) technique, simultaneously. A laser wavelength of 532 nm was focused on the as produced Ag NPs, suspended in an Origanum majorana extract solution, with the aim of controlling their size. The effect of liquid medium concentration and irradiation time on the properties of the fabricated NPs was studied. While the X-ray diffraction (XRD) pattern confirmed the existence of Ag NPs, the UV–Vis spectrophotometry showed a significant absorption peak at about 420 nm, which is attributed to the characteristic surface plasmon resonance (SPR) peak of the obtained Ag NPs. By increasing the irradiation time and the Origanum majora extract concentration, the SPR peak shifted toward a shorter wavelength. This shift indicates a reduction in the NPs’ size. The effect of PLFL on size reduction was clearly revealed from the transmission electron microscopy images. The PLFL technique, depending on experimental parameters, reduced the size of the obtained Ag NPs to less than 10 nm. The mean zeta potential of the fabricated Ag NPs was found to be greater than −30 mV, signifying their stability. The Ag NPs were also found to effectively inhibit bacterial activity. The PLFL technique has proved to be a powerful method for controlling the size of NPs when it is simultaneously associated with a chemical reduction process.

Synthesis and Application of Itaconic Acid Water-Coke Slurry Dispersant

2017 ◽  
Vol 896 ◽  
pp. 167-174 ◽  
Author(s):  
Zhi Yuan Yang ◽  
Zhuo Yue Meng ◽  
Zhi Hua Li ◽  
Si Tong Wang
Keyword(s):  
Surface Tension ◽  
Polyethylene Glycol ◽  
Itaconic Acid ◽  
High Performance ◽  
Ph Value ◽  
Raw Materials ◽  
Esterification Reaction ◽  
Solution Ph ◽  
Powder Surface ◽  
Coke Powder

Polyethylene glycol (PEG-200) and itaconic acid (IA) were used as raw materials to compound macromer through esterification reaction. A new type of specialized water-coke slurry dispersant was synthesized by copolymerization of microware, sodium methallyl sulfonate (SMAS) and maleic anhydride (MA). The experiment showed that the concentration of slurry could be reached to 63% with the dosage of 0.2%, and the apparent viscosity was 1140.3 mPa∙s. Through the analysis of the infrared, the dispersant was confirmed to have polyethylene glycol branched chain and hydrophilic functional groups such as carboxyl or sulfonic group. When the concentration of dispersant was 30 g/L, the surface tension of water could be decreased from 72.70 mN/m to 45.50 mN/m. Furthermore, when the solution pH value was 9, the Zeta potential of semi-coke powder surface could also be decreased from-13.38 mV to-25 mV with the addition of dispersant. Thus, this dispersant could increase electronegativity of semi-coke powder surface, enhance steric-hindrance effect and prevent the phenomenon of powder flocculation and gather. Meantime, it also could reinforce the semi-coke hydrophilic by reducing the surface tension of water effectively. And then, the high performance water-coke slurry could be obtained.

The effect of silver concentration and calcination temperature on structural and optical properties of ZnO:Ag nanoparticles

2015 ◽  
Vol 29 (01) ◽  
pp. 1450254 ◽  
Author(s):  
M. Shayani Rad ◽  
A. Kompany ◽  
A. Khorsand Zak ◽  
M. E. Abrishami
Keyword(s):  
Calcination Temperature ◽  
Sol Gel ◽  
Visible Emission ◽  
X Ray Diffraction ◽  
Ag Nps ◽  
Zno Nps ◽  
Calcination Temperatures ◽  
Transmission Electron ◽  
Xrd Patterns ◽  
Average Size

Pure and silver added zinc oxide nanoparticles ( ZnO -NPs and ZnO : Ag -NPs) were synthesized through a modified sol–gel method. The prepared samples were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM) and photoluminescence (PL) spectroscopy. In the XRD patterns, silver diffracted peaks were also observed for the samples synthesized at different calcination temperatures of 500°C, 700°C, 900°C except 1100°C, in addition to ZnO . TEM images indicated that the average size of ZnO : Ag -NPs increases with the amount of Ag concentration. The PL spectra of the samples revealed that the increase of Ag concentration results in the increase of the visible emission intensity, whereas by increasing the calcination temperature the intensity of visible emission of the samples decreases.

Effect of Yttria-Stabilized Zirconia Concentration in an Electroless Bath on Microstructure and Composition of Ni/Yttria-Stabilized Zirconia Nanocomposite

2021 ◽  
Vol 21 (11) ◽  
pp. 5592-5602
Author(s):  
Samira Almasi ◽  
Ali Mohammad Rashidi
Keyword(s):  
High Performance ◽  
Yttria Stabilized Zirconia ◽  
X Ray Diffraction ◽  
Stabilized Zirconia ◽  
Nickel Ion ◽  
Nanocomposite Particles ◽  
X Ray ◽  
Ni Content ◽  
Naoh Solution ◽  
Average Size

The effect of the yttria-stabilized zirconia (YSZ) nanoparticle loading in an electro-less bath was considered as one of the vital synthesis variables for control Ni content and microstructure of prepared nanocomposite particles, which are two crucial factors to achieving high-performance SOFC anode. Nanocomposite particles were prepared using a simple electroless method without any expensive pretreatment of sensitizing by Sn2+ ions as well as activating by Pd2+ ions that are usually used to apply nickel coating on the surface of a non-conductive substrate. The process was performed by adding YSZ nanoparticles into NaOH solution, separating them from the solution by the centrifugal method, then providing several water-based nanofluids with different concentrations of activated YSZ nanoparticles, mixing them with NiCI2 solution, followed by adding the hydrazine and then NaOH solution. X-ray diffraction and scanning electron microscopy coupled with energy dispersive X-ray analysis were used to analyze the prepared nanocomposite particles. It is observed that after adding YSZ nanoparticles into the NaOH solution, the pH of the solution varied gradually from a starting pH of 10.2 to 9. Also, by increasing the YSZ nanoparticles loading in the electroless bath from 76 mg/l to 126 mg/l, the grain size of Ni deposits, the Ni content and the average size of the prepared nanocomposite particles decreased. The electrochemical mechanism previously proposed for the nickel ion reduction was modified, and a novel analytical model was proposed for variation of the efficiency of Ni deposition with YSZ nanoparticles loading.

Hydrothermal Synthesis of Rod-Like Copper Oxide Crystals

2007 ◽  
Vol 534-536 ◽  
pp. 77-80 ◽  
Author(s):  
Jae Hwan Pee ◽  
Dong Wook Lee ◽  
Ungsoo Kim ◽  
Eui Seok Choi
Keyword(s):  
Copper Oxide ◽  
Ph Value ◽  
Copper Nitrate ◽  
Synthesis Temperature ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
X Ray Diffraction ◽  
Solution Ph ◽  
Uniform Size ◽  
Oxide Crystals

A hyrdrothermal reaction process has been developed to prepare rod-like crystals of copper oxide using copper nitrate trihydrate as a function of synthesis temperature, stirring speed and solution pH value. The properties of the fabricated crystals were studied using scanning electron microscopy, X-ray diffraction and particle size analysis. The morphology of the synthesized CuO was dependent on both the pH value of the solution and the morphology of the seed materials. Synthesized particles have regular morphologies and a uniform size distribution.

scholarly journals Ce-Doped PANI/Fe3O4 Nanocomposites: Electrode Materials for Supercapattery

2021 ◽  
Vol 3 ◽  
Author(s):  
Subash Pandey ◽  
Shova Neupane ◽  
Dipak Kumar Gupta ◽  
Anju Kumari Das ◽  
Nabin Karki ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Electrode Material ◽  
High Performance ◽  
Electrode Materials ◽  
Specific Capacity ◽  
Maximum Energy ◽  
Potential Range ◽  
X Ray Diffraction ◽  
Active Electrode ◽  
Transmission Electron

In this study, we report on a combined approach to preparing an active electrode material for supercapattery application by making nanocomposites of Polyaniline/Cerium (PANI/Ce) with different weight percentages of magnetite (Fe3O4). Fourier-transform infrared spectroscopy (FTIR) and x-ray diffraction (XRD) analyses supported the interaction of PANI with Ce and the formation of the successful nanocomposite with magnetite nanoparticles. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses showed the uniform and porous morphology of the composites. Cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) were used to test the supercapattery behavior of the nanocomposite electrodes in 1.0 M H2SO4. It was found that the supercapattery electrode of PANI/Ce+7 wt.% Fe3O4 exhibited a specific capacity of 171 mAhg−1 in the potential range of −0.2 to 1.0 V at the current density of 2.5 Ag−1. Moreover, PANI/Ce+7 wt.% Fe3O4 revealed a power density of 376.6 Wkg−1 along with a maximum energy density of 25.4 Whkg−1 at 2.5 Ag−1. Further, the cyclic stability of PANI/Ce+7 wt.% Fe3O4 was found to be 96.0% after 5,000 cycles. The obtained results suggested that the PANI/Ce+Fe3O4 nanocomposite could be a promising electrode material candidate for high-performance supercapattery applications.

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