scholarly journals Controllability of cupric particle synthesis by linear alcohol chain number as additive and pH control in cupric acetate solution using X-ray radiolysis

2019 ◽  
Vol 26 (6) ◽  
pp. 1986-1995 ◽  
Author(s):  
Akinobu Yamaguchi ◽  
Ikuo Okada ◽  
Ikuya Sakurai ◽  
Hirokazu Izumi ◽  
Mari Ishihara ◽  
...  
Keyword(s):  
Aqueous Solutions ◽  
Chain Length ◽  
Cupric Oxide ◽  
Liquid Solution ◽  
Ph Control ◽  
Acetate Solution ◽  
Reaction Route ◽  
X Ray ◽  
Rate Of Reaction ◽  
Oxide Particles

Synthesis and immobilization of caltrop cupric particles onto a Si substrate using X-ray radiolysis directly from a liquid solution of Cu(COOCH3)2 is demonstrated. Caltrop cupric oxide particles are formed in the X-ray radiolysis of aqueous solutions of Cu(COOCH3)2, which also contain methanol, ethanol, 2-propanol or 1-propanol as ^\bulletOH scavenger. The blade lengths of the caltrop particles are dependent on the alcohol chain length. In particular, it was found that an alkyl alcohol whose chain length is longer than four is unable to synthesize any particles in aqueous solutions of Cu(COOCH3)2 in X-ray radiolysis. These results are attributed to the alkyl alcohol chain length influencing the rate of reaction of radicals and determines the solvable ratio of its alcohol into water. In addition, it was found that the synthesized particle geometric structure and composition can also be controlled by the pH of the aqueous solution in the X-ray radiolysis. This study may open a door to understanding and investigating a novel photochemical reaction route induced under X-ray irradiation. The development of the X-ray radiolysis process enables us to achieve the rapid and easy process of synthesis and immobilization of higher-order nano/microstructure consisting of various materials.

scholarly journals One-Step Synthesis of Copper and Cupric Oxide Particles from the Liquid Phase by X-Ray Radiolysis Using Synchrotron Radiation

2016 ◽  
Vol 2016 ◽  
pp. 1-16 ◽  
Author(s):  
Akinobu Yamaguchi ◽  
Ikuo Okada ◽  
Takao Fukuoka ◽  
Mari Ishihara ◽  
Ikuya Sakurai ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Synchrotron Radiation ◽  
Cupric Oxide ◽  
Oxide Particle ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
One Step ◽  
Oxide Particles

The deposition of copper (Cu) and cupric oxide (Cu4O3, Cu2O, and CuO) particles in an aqueous copper sulfate (CuSO4) solution with additive alcohol such as methanol, ethanol, 2-propanol, and ethylene glycol has been studied by X-ray exposure from synchrotron radiation. An attenuated X-ray radiation time of 5 min allows for the synthesis of Cu, Cu4O3, Cu2O, and CuO nano/microscale particles and their aggregation into clusters. The morphology and composition of the synthesized Cu/cupric oxide particle clusters were characterized by scanning electron microscopy, scanning transmission electron microscopy, and high-resolution transmission electron microscopy with energy dispersive X-ray spectroscopy. Micro-Raman spectroscopy revealed that the clusters comprised cupric oxide core particles covered with Cu particles. Neither Cu/cupric oxide particles nor their clusters were formed without any alcohol additives. The effect of alcohol additives is attributed to the following sequential steps: photochemical reaction due to X-ray irradiation induces nucleation of the particles accompanying redox reaction and forms a cluster or aggregates by LaMer process and DLVO interactions. The procedure offers a novel route to synthesize the Cu/cupric oxide particles and aggregates. It also provides a novel additive manufacturing process or lithography of composite materials such as metal, oxide, and resin.

Caltrop particles synthesized by photochemical reaction induced by X-ray radiolysis

2017 ◽  
Vol 24 (3) ◽  
pp. 653-660 ◽  
Author(s):  
Akinobu Yamaguchi ◽  
Takao Fukuoka ◽  
Iukuo Okada ◽  
Mari Ishihara ◽  
Ikuya Sakurai ◽  
...  
Keyword(s):  
Room Temperature ◽  
Cupric Oxide ◽  
Synthetic Methods ◽  
Raman Spectrometry ◽  
Synchrotron Source ◽  
X Ray ◽  
Oxide Particles ◽  
Synthetic Routes ◽  
Micrometer Scale ◽  
Electron Donation

X-ray radiolysis of a Cu(CH3COO)2 solution was observed to produce caltrop-shaped particles of cupric oxide (CuO, Cu2O), which were characterized using high-resolution scanning electron microscopy and micro-Raman spectrometry. X-ray irradiation from a synchrotron source drove the room-temperature synthesis of submicrometer- and micrometer-scale cupric oxide caltrop particles from an aqueous Cu(CH3COO)2 solution spiked with ethanol. The size of the caltrop particles depended on the ratio of ethanol in the stock solution and the surface of the substrate. The results indicated that there were several synthetic routes to obtain caltrop particles, each associated with electron donation. The technique of X-ray irradiation enables the rapid synthesis of caltrop cupric oxide particles compared with conventional synthetic methods.

The Equilibrium Constant for the Formation of Al2(OH)24+ in Aqueous Solutions

1975 ◽  
Vol 53 (19) ◽  
pp. 2811-2817 ◽  
Author(s):  
R. C. Turner
Keyword(s):  
Ionic Strength ◽  
Aqueous Solutions ◽  
Equilibrium Constant ◽  
Sodium Acetate ◽  
Sodium Acetate Solution ◽  
Acetate Solution ◽  
Rate Of Reaction

The equilibrium constant for the formation of the aluminum hydroxy dimer, Al2(OH)24+, was calculated from measured values of pH and the concentrations of the dimer and trivalent aluminum in aqueous solutions at 25 °C. The concentrations of Al2(OH)24+ was determined by a method based on its rate of reaction with an 8-hydroxyquinoline – sodium acetate solution. Experiments were made with various concentrations of aluminum and different ionic strengths. With an ionic strength of 0.06, the equilibrium constant was 10−7.42 and increased with decreasing ionic strength. The negative log of the equilibrium constant when the ionic strength approaches zero was estimated to be 6.95 ± 0.05.

Electrodeposition of Cu2O Particles by Using Electrolyte Solution Containing Glucopone as Surfactant

2009 ◽  
Vol 1 (2) ◽  
pp. 18-20
Author(s):  
Dahyunir Dahlan
Keyword(s):  
Indium Tin Oxide ◽  
Pulse Current ◽  
Platinum Electrode ◽  
Saturated Calomel Electrode ◽  
X Ray Diffraction ◽  
X Ray ◽  
Glass Substrates ◽  
Continuous Current ◽  
Oxide Particles ◽  
Cupric Sulphate

Copper oxide particles were electrodeposited onto indium tin oxide (ITO) coated glass substrates. Electrodeposition was carried out in the electrolyte containing cupric sulphate, boric acid and glucopone. Both continuous and pulse currents methods were used in the process with platinum electrode, saturated calomel electrode (SCE) and ITO electrode as the counter, reference and working electrode respectively. The deposited particles were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). It was found that, using continuous current deposition, the deposited particles were mixture of Cu2O and CuO particles. By adding glucopone in the electrolyte, particles with spherical shapes were produced. Electrodeposition by using pulse current, uniform cubical shaped Cu2O particles were produced

A Facile Synthesis of Cu2O and CuO Nanoparticles Via Sonochemical Assisted Method

2018 ◽  
Vol 15 (2) ◽  
pp. 209-213 ◽  
Author(s):  
Sathish Mohan Botsa ◽  
Ramadevi Dharmasoth ◽  
Keloth Basavaiah
Keyword(s):  
Diffuse Reflectance Spectroscopy ◽  
Cupric Oxide ◽  
Copper Acetate ◽  
Chemical Properties ◽  
Copper Oxide Nanoparticles ◽  
Reducing Agents ◽  
Sonochemical Method ◽  
Phase Purity ◽  
X Ray ◽  
Cuo Nps

Background: During past two decades, functional nanomaterials have received great attention for many technological applications such as catalysis, energy, environment, medical and sensor due to their unique properties at nanoscale. However, copper oxide nanoparticles (NPs) such as CuO and Cu2O have most widely investigated for many potential applications due to their wide bandgap, high TC, high optical absorption and non-toxic in nature. The physical and chemical properties of CuO and Cu2O NPs are critically depending on their size, morphology and phase purity. Therefore, lots of efforts have been done to prepare phase CuO and Cu2O NPs with different morphology and size. Method: The synthesis of cupric oxide (CuO) and cuprous oxide (Cu2O) NPs using copper acetate as a precursor by varying the reducing agents such as hydrazine sulphate and hydrazine hydrate via sonochemical method. The phase, morphology and crystalline structure of a prepared CuO and Cu2O NPs were investigated by X-ray diffraction (XRD), Fourier transform infrared (FTIR), Field emission scanning electron microscopy (FESEM), Energy dispersive X-ray (EDS) and UV-Visible Diffuse reflectance spectroscopy (DRS). Results: The phase of NPs was tuned as a function of reducing agents.XRD patterns confirmed the formation of pure phase crystalline CuO and Cu2O NPs. FTIR peak at 621 cm-1 confirmed Cu(I)-O vibrations, while CuO vibrations confirmed by the presence of two peaks at 536 and 586 cm-1. Further investigation was done by Raman, which clearly indicates the presence of peaks at 290, 336, 302 cm-1 and 173, 241 cm-1 for CuO and Cu2O NPs, respectively. The FESEM images revealed rod-like morphology of the CuO NPs while octahedral like shape for Cu2O NPs. The presence of elemental Cu and O in stoichiometric ratios in EDS spectra confirms the formation of both CuO and Cu2O NPs. In summary, CuO and Cu2O NPs were successfully synthesized by a sonochemical method using copper acetate as a precursor at different reducing agents. The bandgap of CuO and Cu2O NPs was 2.38 and 1.82, respectively. Furthermore, the phase purity critically depends on reducing agents.

scholarly journals Preparation and Characterization of the Sulfur-Impregnated Natural Zeolite Clinoptilolite for Hg(II) Removal from Aqueous Solutions

Processes ◽  
2021 ◽  
Vol 9 (2) ◽  
pp. 217
Author(s):  
Marin Ugrina ◽  
Martin Gaberšek ◽  
Aleksandra Daković ◽  
Ivona Nuić
Keyword(s):  
Chemical Modification ◽  
Aqueous Solutions ◽  
Specific Surface ◽  
Surface Area ◽  
Natural Zeolite ◽  
Contact Time ◽  
Liquid Ratio ◽  
X Ray ◽  
Solid Liquid

Sulfur-impregnated zeolite has been obtained from the natural zeolite clinoptilolite by chemical modification with Na2S at 150 °C. The purpose of zeolite impregnation was to enhance the sorption of Hg(II) from aqueous solutions. Chemical analysis, acid and basic properties determined by Bohem’s method, chemical behavior at different pHo values, zeta potential, cation-exchange capacity (CEC), specific surface area, X-ray powder diffraction (XRPD), scanning electron microscopy with energy-dispersive X-ray analysis (SEM-EDS), Fourier transform infrared spectroscopy (FTIR), as well as thermogravimetry with derivative thermogravimetry (TG-DTG) were used for detailed comparative mineralogical and physico-chemical characterization of natural and sulfur-impregnated zeolites. Results revealed that the surface of the natural zeolite was successfully impregnated with sulfur species in the form of FeS and CaS. Chemical modification caused an increase in basicity and the net negative surface charge due to an increase in oxygen-containing functional groups as well as a decrease in specific surface area and crystallinity due to the formation of sulfur-containing clusters at the zeolite surface. The sorption of Hg(II) species onto the sulfur-impregnated zeolite was affected by the pH, solid/liquid ratio, initial Hg(II) concentration, and contact time. The optimal sorption conditions were determined as pH 2, a solid/liquid ratio of 10 g/L, and a contact time of 800 min. The maximum obtained sorption capacity of the sulfur-impregnated zeolite toward Hg(II) was 1.02 mmol/g. The sorption mechanism of Hg(II) onto the sulfur-impregnated zeolite involves electrostatic attraction, ion exchange, and surface complexation, accompanied by co-precipitation of Hg(II) in the form of HgS. It was found that sulfur-impregnation enhanced the sorption of Hg(II) by 3.6 times compared to the natural zeolite. The leaching test indicated the retention of Hg(II) in the zeolite structure over a wide pH range, making this sulfur-impregnated sorbent a promising material for the remediation of a mercury-polluted environment.

Green synthesized Ag-TiO2 for degradation of organic dye through visible light driven photo-reactor and its kinetics

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Titikshya Mohapatra ◽  
Sakshi Manekar ◽  
Vijyendra Kumar Sahu ◽  
Ashwini Kumar Soni ◽  
Sudip Banerjee ◽  
...  
Keyword(s):  
Visible Light ◽  
Mangifera Indica ◽  
Band Gap Energy ◽  
Photo Degradation ◽  
X Ray ◽  
Green Approach ◽  
Vis Spectroscopy ◽  
Rate Of Reaction ◽  
Visible Light Driven ◽  
Modification Of Titanium

Abstract This study reports a green approach for the modification of titanium dioxide (TiO2) nanoparticles with immobilization of silver nanoparticles. One of the natural sources i.e., Mangifera indica leaf extract was utilized as reducing and capping agent for the fabrication of Ag-TiO2 nanocatalyst. Further, the surface morphology and band-gap energy of prepared Ag-TiO2 were analyzed by Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Spectroscopy (EDS) and UV–Vis spectroscopy. Also, it was characterized by X-ray Powder Diffraction (XRD) which provides the information regarding the crystallinity of the Ag-TiO2. Subsequently, photo activity of Ag-TiO2 was investigated for the degradation of methylene blue (MB) dye wastewater through visible light driven photoreactor. The Ag-TiO2 provided highest (68%) of photo-degradation efficiency within 110 min for 7.81 × 10−5 mol/L initial MB concentration at pH 8 by using 0.19 g/L photocatalyst. Further, addition of 10 mM H2O2 boost up the MB photodegradation to 74%. The kinetic study confirmed the MB degradation followed first order rate of reaction.

scholarly journals Structure of aqueous sodium acetate solutions by X-Ray scattering and density functional theory

2020 ◽  
Vol 92 (10) ◽  
pp. 1627-1641
Author(s):  
Guangguo Wang ◽  
Yongquan Zhou ◽  
He Lin ◽  
Zhuanfang Jing ◽  
Hongyan Liu ◽  
...  
Keyword(s):  
Sodium Acetate ◽  
Density Functional ◽  
Hydration Shell ◽  
Ion Pair ◽  
Water Molecules ◽  
Sodium Acetate Solution ◽  
Acetate Solution ◽  
X Ray ◽  
X Ray Scattering ◽  
Ray Scattering

AbstractThe structure of aq. sodium acetate solution (CH3COONa, NaOAc) was studied by X-ray scattering and density function theory (DFT). For the first hydrated layer of Na+, coordination number (CN) between Na+ and O(W, I) decreases from 5.02 ± 0.85 at 0.976 mol/L to 3.62 ± 1.21 at 4.453 mol/L. The hydration of carbonyl oxygen (OC) and hydroxyl oxygen (OOC) of CH3COO− were investigated separately and the OC shows a stronger hydration bonds comparing with OOC. With concentrations increasing, the hydration shell structures of CH3COO− are not affected by the presence of large number of ions, each CH3COO− group binds about 6.23 ± 2.01 to 7.35 ± 1.73 water molecules, which indicates a relatively strong interaction between CH3COO− and water molecules. The larger uncertainty of the CN of Na+ and OC(OOC) reflects the relative looseness of Na-OC and Na-OOC ion pairs in aq. NaOAc solutions, even at the highest concentration (4.453 mol/L), suggesting the lack of contact ion pair (CIP) formation. In aq. NaOAc solutions, the so called “structure breaking” property of Na+ and CH3COO− become effective only for the second hydration sphere of bulk water. The DFT calculations of CH3COONa (H2O)n=5–7 clusters suggest that the solvent-shared ion pair (SIP) structures appear at n = 6 and become dominant at n = 7, which is well consistent with the result from X-ray scattering.

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