Effect of nano-sized cerium–zirconium oxide solid solution on far-infrared emission properties of tourmaline powders

2015 ◽  
Vol 29 (30) ◽  
pp. 1550183 ◽  
Author(s):  
Bin Guo ◽  
Liqing Yang ◽  
Weijie Hu ◽  
Wenlong Li ◽  
Haojing Wang
Keyword(s):  
Photoelectron Spectroscopy ◽  
Raw Materials ◽  
Reference Sample ◽  
Far Infrared ◽  
Infrared Emission ◽  
Emission Property ◽  
Precipitation Method ◽  
Xps Spectra ◽  
X Ray ◽  
Emission Properties

Far-infrared functional nanocomposites were prepared by the co-precipitation method using natural tourmaline [Formula: see text], where [Formula: see text] is [Formula: see text], [Formula: see text], [Formula: see text], or vacancy; [Formula: see text] is [Formula: see text], [Formula: see text], [Formula: see text], [Formula: see text], [Formula: see text], [Formula: see text], [Formula: see text], [Formula: see text], or [Formula: see text]; [Formula: see text] is [Formula: see text], [Formula: see text], [Formula: see text], or [Formula: see text]; [Formula: see text] is [Formula: see text], [Formula: see text]; and [Formula: see text] is [Formula: see text], [Formula: see text], or [Formula: see text] powders, ammonium cerium(IV) nitrate and zirconium(IV) nitrate pentahydrate as raw materials. The reference sample, tourmaline modified with ammonium cerium(IV) nitrate alone was also prepared by a similar precipitation route. The results of Fourier transform infrared spectroscopy show that tourmaline modified with Ce and Zr has a better far-infrared emission property than tourmaline modified with Ce alone. Through characterization by transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS), the mechanism for oxygen evolution during the heat process in the two composite materials was systematically studied. The XPS spectra show that [Formula: see text] ratio inside tourmaline modified with Ce alone can be raised by doping Zr. Moreover, it is showed that there is a higher [Formula: see text] ratio inside the tourmaline modified with Ce and Zr than tourmaline modified with Ce alone. In addition, XRD results indicate the formation of [Formula: see text] and [Formula: see text] crystallites during the heat treatment and further TEM observations show they exist as nanoparticles on the surface of tourmaline powders. Based on these results, we attribute the improved far-infrared emission properties of Ce–Zr doped tourmaline to the enhanced unit cell shrinkage of the tourmaline arisen from much more oxidation of [Formula: see text] to [Formula: see text] inside the tourmaline caused by the change in the catalyst redox properties of [Formula: see text] brought about by doping with [Formula: see text]. In all samples, tourmaline modified with 7.14 wt.% Ce and 1.86 wt.% Zr calcined at 800[Formula: see text]C for 5 h has the best far-infrared emission property with the maximum emissivity value of 98%.

scholarly journals Preparation of Micro-Nano Material Composed of Oyster Shell/Fe3O4 Nanoparticles/Humic Acid and Its Application in Selective Removal of Hg(II)

Nanomaterials ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 953 ◽  
Author(s):  
Chuxian He ◽  
Junhao Qu ◽  
Zihua Yu ◽  
Daihuan Chen ◽  
Tiantian Su ◽  
...  
Keyword(s):  
Humic Acid ◽  
Fe3o4 Nanoparticles ◽  
Photoelectron Spectroscopy ◽  
Raw Materials ◽  
Oyster Shell ◽  
Solution Concentration ◽  
Precipitation Method ◽  
Maximum Adsorption Capacity ◽  
X Ray ◽  
Isotherm Equation

Micro-nano composite material was prepared to adsorb Hg(II) ions via the co-precipitation method. Oyster shell (OS), Fe3O4 nanoparticles, and humic acid (HA) were used as the raw materials. The adhesion of nanoparticles to OS displayed by scanning electron microscopy (SEM), the appearance of the (311) plane of standard Fe3O4 derived from X-ray diffraction (XRD), and the transformation of pore sizes to 50 nm and 20 μm by mercury intrusion porosimetry (MIP) jointly revealed the successful grafting of HA-functionalized Fe3O4 onto the oyster shell surface. The vibrating sample magnetometer (VSM) results showed superparamagnetic properties of the novel adsorbent. The adsorption mechanism was investigated based on X-ray photoelectron spectroscopy (XPS) techniques, which showed the process of physicochemical adsorption while mercury was adsorbed as Hg(II). The effects of pH (3–7), initial solution concentration (2.5–30 mg·L−1), and contact time (0–5 h) on the adsorption of Hg(II) ions were studied in detail. The experimental data were well fitted to the Langmuir isotherm equation (R2 = 0.991) and were shown to follow a pseudo-second-order reaction model (R2 = 0.998). The maximum adsorption capacity of Hg(II) was shown to be 141.57 mg·g−1. In addition, this new adsorbent exhibited excellent selectivity.

Effect of the Dosage of Tourmaline on Far Infrared Emission Properties of Tourmaline/Glass Composite Materials

2016 ◽  
Vol 16 (4) ◽  
pp. 3899-3903 ◽  
Author(s):  
Hongchen Zhang ◽  
Junping Meng ◽  
Jinsheng Liang ◽  
Jie Liu ◽  
Zhaoyang Zeng
Keyword(s):  
Particle Size ◽  
Composite Materials ◽  
Raw Materials ◽  
Far Infrared ◽  
Infrared Emission ◽  
Infrared Emissivity ◽  
Glass Composite ◽  
Emission Properties ◽  
The Fourier Transform ◽  
Glass Powders

Tourmaline/glass composite materials were prepared by sintering at 600 °C using micron-size tourmaline mineral and glass powders as raw materials. The glass has lower melting point than the transition temperature of tourmaline. The Fourier transform infrared spectroscopy showed that the far infrared emissivity of composite was significantly higher than that of either tourmaline or glass powders. A highest far infrared emissivity of 0.925 was obtained when the dosage of tourmaline was 10 wt%. The effects of the amount of tourmaline on the far infrared emission properties of composite was also systematically studied by field emission scanning electron microscope and X-ray diffraction. The tourmaline phase was observed in the composite, showing a particle size of about 70 nm. This meant that the tourmaline particles showed nanocrystallization. They distributed homogenous in the glass matrix when the dosage of tourmaline was not more than 20 wt%. Two reasons were attributed to the improved far infrared emission properties of composite: the particle size of tourmaline-doped was nanocrystallized and the oxidation of Fe2+ (0.076 nm in radius) to Fe3+ (0.064 nm in radius) took place inside the tourmaline-doped. This resulted in the shrinkage of unit cell of the tourmaline in the composite.

scholarly journals Effect of lanthanum doping on the far-infrared emission property of vanadium–titanium slag ceramic

RSC Advances ◽  
2017 ◽  
Vol 7 (22) ◽  
pp. 13509-13516 ◽  
Author(s):  
Kewei Zhang ◽  
Yi Deng ◽  
Yuanyi Yang ◽  
Yongkang Liao ◽  
Bozhi Wang ◽  
...  
Keyword(s):  
Solid Waste ◽  
Raw Materials ◽  
Far Infrared ◽  
Infrared Emission ◽  
Emission Property ◽  
Titanium Slag ◽  
Lanthanum Doping ◽  
Vanadium Titanium

In the present study, a series of far-infrared ceramics were successfully synthesized using vanadium–titanium slag solid waste and some ordinary minerals as main raw materials with lanthanum (La) as an additive.

Effect of heat treatment on structure, surface composition, infrared emission and surface electrical properties of tourmaline

2017 ◽  
Vol 31 (04) ◽  
pp. 1750026 ◽  
Author(s):  
Dengliang He ◽  
Shuxin Liu
Keyword(s):  
Heat Treatment ◽  
Electrical Properties ◽  
Zeta Potential ◽  
Photoelectron Spectroscopy ◽  
Surface Composition ◽  
Functional Materials ◽  
Infrared Emission ◽  
X Ray ◽  
Emission Properties ◽  
Structure Surface

Crystal structure, surface composition, infrared emission properties and surface electrical properties of tourmaline from Guangxi of China, when subjected to heat treatment in air atmosphere had been studied by some methods, including X-ray fluorescence spectrum (XRF), X-ray diffraction (XRD) meter, Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), energy dispersion spectroscopy (EDS), scanning electron microscope (SEM) and Zeta potential analyzer, etc. Experimental results show that the unit cell of tourmaline would shrink during heat treatment because Fe[Formula: see text] were oxidized. Moreover, the Fe[Formula: see text]/Fe[Formula: see text] inside tourmaline can be raised after treatment. Infrared normal total emissivity of tourmaline reaches 0.87, and infrared radiation energy density is [Formula: see text]. It can maintain excellent infrared emission properties at high temperature. Simultaneously, tourmaline presents negative Zeta potential in the aqueous solution, and its Zeta potential reaches −18.04 mV. Zeta potential of tourmaline was increased to −24.83 mV after heat treatment at 400[Formula: see text]C, and decrease to −11.78 mV after heat treatment at 600[Formula: see text]C. These findings may provide reference data for tourmaline’s application in the field of functional materials.

scholarly journals Preparation of LiFePO4/C Cathode Materials via a Green Synthesis Route for Lithium-Ion Battery Applications

Materials ◽  
2018 ◽  
Vol 11 (11) ◽  
pp. 2251 ◽  
Author(s):  
Rongyue Liu ◽  
Jianjun Chen ◽  
Zhiwen Li ◽  
Qing Ding ◽  
Xiaoshuai An ◽  
...  
Keyword(s):  
Cathode Materials ◽  
Photoelectron Spectroscopy ◽  
Raw Materials ◽  
Lithium Ion ◽  
Lithium Carbonate ◽  
Electrochemical Performances ◽  
Scanning Calorimetry ◽  
Xps Spectra ◽  
X Ray ◽  
Exhaust Purification

In this work, LiFePO4/C composite were synthesized via a green route by using Iron (III) oxide (Fe2O3) nanoparticles, Lithium carbonate (Li2CO3), glucose powder and phosphoric acid (H3PO4) solution as raw materials. The reaction principles for the synthesis of LiFePO4/C composite were analyzed, suggesting that almost no wastewater and air polluted gases are discharged into the environment. The morphological, structural and compositional properties of the LiFePO4/C composite were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), Raman and X-ray photoelectron spectroscopy (XPS) spectra coupled with thermogravimetry/Differential scanning calorimetry (TG/DSC) thermal analysis in detail. Lithium-ion batteries using such LiFePO4/C composite as cathode materials, where the loading level is 2.2 mg/cm2, exhibited excellent electrochemical performances, with a discharge capability of 161 mA h/g at 0.1 C, 119 mA h/g at 10 C and 93 mA h/g at 20 C, and a cycling stability with 98.0% capacity retention at 1 C after 100 cycles and 95.1% at 5 C after 200 cycles. These results provide a valuable approach to reduce the manufacturing costs of LiFePO4/C cathode materials due to the reduced process for the polluted exhaust purification and wastewater treatment.

scholarly journals Improved Water–Gas Shift Performance of Au/NiAl LDHs Nanostructured Catalysts via CeO2 Addition

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 366
Author(s):  
Margarita Gabrovska ◽  
Ivan Ivanov ◽  
Dimitrinka Nikolova ◽  
Jugoslav Krstić ◽  
Anna Maria Venezia ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Nanostructured Catalysts ◽  
Water Gas Shift ◽  
Precipitation Method ◽  
Conversion Degree ◽  
Pure Hydrogen ◽  
Medium Temperature ◽  
X Ray ◽  
Supported Gold ◽  
Water Gas

Supported gold on co-precipitated nanosized NiAl layered double hydroxides (LDHs) was studied as an effective catalyst for medium-temperature water–gas shift (WGS) reaction, an industrial catalytic process traditionally applied for the reduction in the amount of CO in the synthesis gas and production of pure hydrogen. The motivation of the present study was to improve the performance of the Au/NiAl catalyst via modification by CeO2. An innovative approach for the direct deposition of ceria (1, 3 or 5 wt.%) on NiAl-LDH, based on the precipitation of Ce3+ ions with 1M NaOH, was developed. The proposed method allows us to obtain the CeO2 phase and to preserve the NiAl layered structure by avoiding the calcination treatment. The synthesis of Au-containing samples was performed through the deposition–precipitation method. The as-prepared and WGS-tested samples were characterized by X-ray powder diffraction, N2-physisorption and X-ray photoelectron spectroscopy in order to clarify the effects of Au and CeO2 loading on the structure, phase composition, textural and electronic properties and activity of the catalysts. The reduction behavior of the studied samples was evaluated by temperature-programmed reduction. The WGS performance of Au/NiAl catalysts was significantly affected by the addition of CeO2. A favorable role of ceria was revealed by comparison of CO conversion degree at 220 °C reached by 3 wt.% CeO2-modified and ceria-free Au/NiAl samples (98.8 and 83.4%, respectively). It can be stated that tuning the properties of Au/NiAl LDH via CeO2 addition offers catalysts with possibilities for practical application owing to innovative synthesis and improved WGS performance.

scholarly journals Optical, XPS and XRD Studies of Semiconducting Copper Sulfide Layers on a Polyamide Film

2009 ◽  
Vol 2009 ◽  
pp. 1-8 ◽  
Author(s):  
Valentina Krylova ◽  
Mindaugas Andrulevičius
Keyword(s):  
Photoelectron Spectroscopy ◽  
Copper Sulfide ◽  
Diffusion Method ◽  
X Ray Diffraction ◽  
Xps Spectra ◽  
X Ray ◽  
Xrd Studies ◽  
Polyamide Film ◽  
Indirect Band Gap ◽  
Xrd Method

Copper sulfide layers were formed on polyamide PA 6 surface using the sorption-diffusion method. Polymer samples were immersed for 4 and 5 h in 0.15 mol⋅  solutions and acidified with HCl (0.1 mol⋅) at . After washing and drying, the samples were treated with Cu(I) salt solution. The samples were studied by UV/VIS, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) methods. All methods confirmed that on the surface of the polyamide film a layer of copper sulfide was formed. The copper sulfide layers are indirect band-gap semiconductors. The values of are 1.25 and 1.3 eV for 4 h and 5 h sulfured PA 6 respectively. Copper XPS spectra analyses showed Cu(I) bonds only in deeper layers of the formed film, while in sulfur XPS S 2p spectra dominating sulfide bonds were found after cleaning the surface with ions. It has been established by the XRD method that, beside , the layer contains as well. For PA 6 initially sulfured 4 h, grain size forchalcocite, , was  nm and fordjurleite, , it was 54.17 nm. The sheet resistance of the obtained layer varies from 6300 to 102 .

Magnetic Properties of Bulk Zn0.95-XMnXFe0.05O2 Prepared by Sol-Gel Method and Subsequent Hot Pressing

2011 ◽  
Vol 268-270 ◽  
pp. 356-359 ◽  
Author(s):  
Wen Song Lin ◽  
C. H. Wen ◽  
Liang He
Keyword(s):  
Magnetic Properties ◽  
Photoelectron Spectroscopy ◽  
Raw Materials ◽  
Sol Gel ◽  
Secondary Phase ◽  
X Ray Diffraction ◽  
Gel Method ◽  
X Ray ◽  
Sol Gel Method ◽  
Doped Zno

Mn, Fe doped ZnO powders (Zn0.95-xMnxFe0.05O2, x≤0.05) were synthesized by an ameliorated sol-gel method, using Zn(CH3COO)2, Mn(CH3COO)2and FeCl2as the raw materials, with the addition of vitamin C as a kind of chemical reducer. The resulting powder was subsequently compacted under pressure of 10 MPa at the temperature of 873K in vacuum. The crystal structure and magnetic properties of Zn0.95-xMnxFe0.05O2powder and bulk samples have been investigated by X-ray diffraction (XRD) and vibrating sample magnetometer (VSM). X-ray photoelectron spectroscopy (XPS) was used to study chemical valence of manganese, iron and zinc in the samples. The x-ray diffraction (XRD) results showed that Zn0.95-xMnxFe0.05O (x≤0.05) samples were single phase with the ZnO-like wurtzite structure. No secondary phase was found in the XRD spectrum. X-ray photoelectron spectroscopy (XPS) showed that Fe and Mn existed in Zn0.95-xMnxFe0.05O2samples in Fe2+and Mn2+states. The results of VSM experiment proved the room temperature ferromagnetic properties (RTFP) of Mn, Fe co-doped ZnO samples.

29Si NMR and XPS Investigation of the Structure of Silicon Oxycarbide Glasses Derived from Polysiloxane Precursors

1994 ◽  
Vol 346 ◽  
Author(s):  
R.J.P. Corriu ◽  
D. Leclercq ◽  
P.H. Mutin ◽  
A. Vioux
Keyword(s):  
Solid State ◽  
Photoelectron Spectroscopy ◽  
Solid State Nmr ◽  
Random Distribution ◽  
Silicon Oxycarbide ◽  
29Si Nmr ◽  
Xps Spectra ◽  
Excess Carbon ◽  
X Ray ◽  
Silicon Oxycarbide Glasses

ABSTRACTTwo silicon oxycarbide glasses with different compositions (O/Si ratio 1.2 and 1.8) were prepared by pyrolysis at moderate temperature (900 °C) of polysiloxane precursors. Their structure was investigated using quantitative 29Si solid-state NMR and X-ray photoelectron spectroscopy (XPS). The environment of the silicon atoms in the oxycarbide phase corresponded to a purely random distribution of Si-O and Si-C bonds depending on the O/Si ratio of the glass only and not on the structure of the precursors. At the light of the NMR results, the Si2p XPS spectra of the glasses may be interpreted using the contribution of the five possible SiOxC4-x tetrahedra. The Cls spectra of these glasses indicated the presence of oxycarbide carbon in CSi4 tetrahedra, similar to carbide carbon, and graphitic-like excess carbon.

Preparation and Characterization of Ni2+-Montmorillonite/Polyvinyl Alcohol Water-Soluble Nanocomposite Film

2005 ◽  
Vol 13 (8) ◽  
pp. 839-846 ◽  
Author(s):  
Li-Ping Wang ◽  
Yun-Pu Wang ◽  
Fa-Ai Zhang
Keyword(s):  
Polyvinyl Alcohol ◽  
Photoelectron Spectroscopy ◽  
Thermal Characteristics ◽  
Water Soluble ◽  
Scanning Calorimetry ◽  
Xps Spectra ◽  
X Ray ◽  
Alcohol Water ◽  
Ft Ir ◽  
Silicate Layers

A new type of nano-composite film was prepared from polyvinyl alcohol, Ni2+-montmorillonite (Ni2+-MMT), defoamer, a levelling agent and a plasticizer. Its thermal characteristics were studied by Differential Scanning Calorimetry (DSC). The intermolecular interactions were measured by Fourier transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS), and the tensile strength (TS) and elongation at break (%E) were measured. The microstructures were studied by X-ray diffraction (XRD) and atomic force microscopy (AFM). FT-IR and XPS spectra indicated that cross-linking has taken place between PVA and Ni2+-MMT. XRD and AFM indicate that the PVA molecules had inserted themselves into the silicate layers of MMT, exfoliating them and dispersing them randomly into the PVA matrix. Compared to pure PVA film, the TS of the films was increased and %E decreased when the Ni2+-Montmorillonite was added and the dissolution temperature of the film was also reduced.

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