Synthesis and Characterization of PVP/Eu4/3L(phen)•2H2O Luminescent Complex

2011 ◽  
Vol 121-126 ◽  
pp. 1500-1503
Author(s):  
Hui Juan Ren ◽  
Hua Yang ◽  
De Hui Sun ◽  
Zhen Feng Cui ◽  
Guang Yan Hong
Keyword(s):  
Electron Microscopy ◽  
Inductively Coupled Plasma ◽  
Atomic Emission ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Pyromellitic Acid ◽  
Inductively Coupled ◽  
Transmission Electron ◽  
Ft Ir

Rare earth europium (Eu(III))-pyromellitic acid (H4L)-1,10-phenanthroline (phen) ternary luminescent complex has been synthesized in polyvinylpyrrolidone (PVP) matrix by precipitation method. The chemical constitution of the complex has been demonstrated as PVP/EuL4/3L(phen)•2H2O by a combination of elemental analysis, inductively coupled plasma-atomic emission spectroscopy (ICP-AES) and Fourier-transform infrared spectroscopy (FT-IR). X-ray diffraction analysis (XRD) has shown that the complex is a new kind of crystal whose structure is totally different from two ligands. The morphology of the complex has been investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The results have shown that the complex has a rodlike crystal structure and the diameter of the rod is about 400 nm. Thermogravimetric analysis (TG) has indicated that the luminescent complex is thermally stable below 300 °C. Photoluminescence spectra (PL) have revealed that the complex can emit Eu3+ characteristic red fluorescence under ultraviolet excitation.

Synthesis and Characterization of Fe2+-CTS/CA-CNTs Composite and its Magnetic Properties

2013 ◽  
Vol 680 ◽  
pp. 49-53
Author(s):  
Chang Yu ◽  
Xu Zhang ◽  
Kan He ◽  
Yue Liu ◽  
Jie Shan Qiu
Keyword(s):  
Electron Microscopy ◽  
Magnetic Properties ◽  
Inductively Coupled Plasma ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Inductively Coupled ◽  
Transmission Electron ◽  
Superparamagnetic State

A novel biocompatible Fe2+-chitosan (CTS)/citric acid modified carbon nanotube (CA-CNTs) composite (Fe2+-CTS/CA-CNTs) has been successfully synthesized by covalent bonding and crosslinking chemistry, followed by the reduction. The samples were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-Vis spectrum, X-ray diffraction (XRD), inductively coupled plasma (ICP), thermal gravimetric analysis (TGA), and vibrating sample magnetometer (VSM) techniques. The results show that the CTS has been successfully grafted to the CA-CNTs carrier and Fe2+ ions are absorbed on the CTS by coordination bond mode. It was found that the Fe2+-CTS/CA-CNTs composite shows good magnetic properties with a low ratio of remanence to saturation magnetization and is in a superparamagnetic state at room temperature. It is believed that the Fe2+-CTS/CA-CNTs composite will be potential for application in MRI.

Synthesis and Characterization of EuL3(phen) Luminescent Complex

2011 ◽  
Vol 239-242 ◽  
pp. 2488-2491
Author(s):  
Hui Juan Ren ◽  
De Hui Sun ◽  
Zhen Feng Cui ◽  
Guang Yan Hong
Keyword(s):  
Inductively Coupled Plasma ◽  
Atomic Emission ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Crystalline Complex ◽  
X Ray ◽  
Inductively Coupled ◽  
Thermogravimetric Curve ◽  
Light Excitation

The europium(III)-benzoic acid(HL)-1,10-phenanthroline(phen) complex was synthesized in the ethanol-H2O system by a precipitation method. The morphology of the minicrystal complex with diameters of ca. 1.0 µm is characterized by scanning electron microscopy (SEM). Elemental analysis and inductively coupled plasma-atomic emission spectroscopy (ICP-AES) are used to determine the chemical composition of the complex. Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction analysis (XRD) are used to examine the structure of the complex. The results show that the complex is a new kind of crystalline complex and the composition of the complex is speculated to be EuL3(phen). The thermogravimetric curve (TGA) analysis indicates that the complex is stable below 232 °C in air. The photoluminescence analyses (PLA) exhibit that the complex emits the characteristic red fluorescence of Eu (III) ions at 613nm under ultraviolet light excitation.

Selective Oxidation of Cyclohexane to Cyclohexanone and Cyclohexanol over Au/Co3O4 Catalyst

2011 ◽  
Vol 284-286 ◽  
pp. 806-810
Author(s):  
Jun Wan ◽  
Jing Zhao ◽  
Ming Qiao Zhu ◽  
Huan Dai ◽  
Lei Wang
Keyword(s):  
Selective Oxidation ◽  
Inductively Coupled Plasma ◽  
Atomic Emission ◽  
Precipitation Method ◽  
Emission Spectrometry ◽  
X Ray Diffraction ◽  
Plasma Atomic Emission Spectrometry ◽  
Inductively Coupled ◽  
Transmission Electron ◽  
Co Precipitation

Au/Co3O4catalysts were prepared by a co-precipitation method and characterized by inductively coupled plasma-atomic emission spectrometry (ICP-AES), transmission electron microscope (TEM) and X-ray diffraction (XRD). The selective oxidation of cyclohexane to cyclohexanone and cyclohexanol was investigated over Au/Co3O4catalysts using molecular oxygen as oxidant. These catalysts showed higher activities as compared to the pure Co3O4under the same reaction conditions.

Synthesis and Characterisation of Tb4L3(Phen)0.75•7H2O Nanorods

2011 ◽  
Vol 194-196 ◽  
pp. 878-881
Author(s):  
Hui Juan Ren ◽  
Zhen Feng Cui ◽  
De Hui Sun ◽  
Guang Yan Hong
Keyword(s):  
Inductively Coupled Plasma ◽  
Atomic Emission ◽  
Precipitation Method ◽  
Rare Earth Complex ◽  
X Ray Diffraction ◽  
Strong Absorption Band ◽  
Inductively Coupled ◽  
Transmission Electron ◽  
Thermogravimetric Curve ◽  
Co Precipitation

The rare earth complex terbium (III)-pyromellitic acid (H4L)-1,10-phenanthroline (phen) nanorod was synthesized in the polyvinylpyrrolidone (PVP) matrix by a co-precipitation method. The chemical composition of the as-synthesized sample was speculated to be PVP/Tb4L3(phen)0.75∙7H2O by elemental analysis, inductively coupled plasma-atomic emission spectroscopy (ICP-AES), and Fourier transform infrared spectroscopy (FTIR). The transmission electron microscopy (TEM) result exhibited that the as-synthesized sample was nanorods with diameters of ca. 150 nm. The X-ray diffraction pattern (XRD) of the sample showed that it was a crystalline complex. The thermogravimetric curve (TGA) analysis exhibited that the sample is stable below 450 °C. UV–Vis diffuse reflectance spectra exhibited that there is a broad and strong absorption band in the range of 280-350 nm. The photoluminescence analyses (PLA) indicated that the as-synthesized sample emitted the characteristic green fluorescence of Tb (III) ions under ultraviolet light excitation.

Facile Synthesis of Basic Magnesium Carbonate with Different Morphology

2012 ◽  
Vol 554-556 ◽  
pp. 575-579 ◽  
Author(s):  
Yun Chuan Yang ◽  
Hong Hao Yu ◽  
Xin Ying Wang
Keyword(s):  
Electron Microscopy ◽  
Inductively Coupled Plasma ◽  
Atomic Emission ◽  
Magnesium Carbonate ◽  
X Ray Diffraction ◽  
Plasma Atomic Emission ◽  
Facile Synthesis ◽  
X Ray ◽  
Inductively Coupled ◽  
Transmission Electron

The preparation of different morphological basic magnesium carbonate particles with hollow rod-like, hull of peanut and leaf from the pyrogenation of magnesium carbonate trihydrate were described. The morphology, crystal phase and purity of basic magnesium carbonate were characterized by scanning electron microscopy(SEM), transmission electron microscopy(TEM), X-ray diffraction (XRD) and inductively coupled plasma atomic emission spectrometer (ICP-AES). The results indicated that the formation of three morphological basic magnesium carbonates were obtained via platelike particles of magnesium carbonate trihydrate under certain conditions where the temperature and stirring rate were properly controlled. The length of the hollow rod means up to 6～7µm, and its diameter means up to 1～2µm.

scholarly journals Pd Nanoparticles Stabilized on the Cross-Linked Melamine-Based SBA-15 as a Catalyst for the Mizoroki–Heck Reaction

2021 ◽  
Author(s):  
Ayat Nuri ◽  
Abolfazl Bezaatpour ◽  
Mandana Amiri ◽  
Nemanja Vucetic ◽  
Jyri-Pekka Mikkola ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Inductively Coupled Plasma ◽  
High Surface ◽  
High Surface Area ◽  
Coupling Reaction ◽  
Pd Nanoparticles ◽  
Significant Activity ◽  
Inductively Coupled ◽  
Transmission Electron ◽  
Ft Ir

AbstractMesoporous SBA-15 silicate with a high surface area was prepared by a hydrothermal method, successively modified by organic melamine ligands and then used for deposition of Pd nanoparticles onto it. The synthesized materials were characterized with infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), nitrogen physisorption, scanning electron microscopy (SEM) coupled with energy dispersive X-ray analysis (EDX), transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) and inductively coupled plasma (ICP-OES). The catalyst was effectively used in the Mizoroki–Heck coupling reaction of various reactants in the presence of an organic base giving the desired products in a short reaction time and with small catalysts loadings. The reaction parameters such as the base type, amounts of catalyst, solvents, and the temperature were optimized. The catalyst was easily recovered and reused at least seven times without significant activity losses. Graphic Abstract

The Characteristic Evaluation of Hydroxyapatite Powders Synthesized from CaCO3 Refined from Oyster Shell and H3PO4

2006 ◽  
Vol 118 ◽  
pp. 639-644
Author(s):  
Hye Sung Kim ◽  
Su Chak Ryu
Keyword(s):  
Bone Density ◽  
Inductively Coupled Plasma ◽  
Oyster Shell ◽  
Atomic Emission ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Inductively Coupled ◽  
Infra Red ◽  
Ft Ir

Hydroxyapatite (Ca10(PO4)6(OH)2, HAp) powders is synthesized using the mixed powders of CaCO3 refined from oyster shells and phosphoric acid (H3PO4-98%, Daejung) as starting materials. The characteristic evaluation and chemical analysis of the synthesized powders is performed by X-ray diffraction (XRD), Fourier-transformed infra-red spectroscopy (FT-IR), and inductively-coupled plasma atomic emission spectroscopy (ICPAES). XRD analysis of synthetic powder by heat treatment at 1300°C for 2hrs shows only HAp peaks corresponding to stoichiometric HAp. It is confirmed by ICP-AES test that impurities such as Zn, In, Ti, Ba, Cd, Pb, and Mn, is not detected at all, but small amounts of Ti and Be is observed (0.099ppm Ti and 0.002ppm Ba). Variation of bone density is measured by giving medication of HAp powder with drinking water into human body continuously for three month. After the medication, the bone density is higher than the medication before. This means that HAp powder made from this process can be used as improver of bone density.

scholarly journals An Efficient and Novel Ammonia Sensor Based on Polypyrrole/Tin Oxide/MWCNT Nanocomposite

2020 ◽  
Vol 32 (6) ◽  
pp. 1505-1510
Author(s):  
Ahmad Husain ◽  
Mohd Urooj Shariq ◽  
Anees Ahmad
Keyword(s):  
Electron Microscopy ◽  
Tin Oxide ◽  
Charge Carriers ◽  
Morphological Properties ◽  
X Ray Diffraction ◽  
Ammonia Sensing ◽  
Transmission Electron ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

In present study, the synthesis and characterization of a novel polypyrrole (PPy)/tin oxide (SnO2)/MWCNT nanocomposite along with pristine polypyrrole is reported. These materials have been studied for their structural and morphological properties by FT-IR spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques. PPy/SnO2/MWCNT nanocomposite has been converted into a pellet-shaped sensor, and its ammonia sensing studies were carried out by calculating the variation in the DC electrical conductivity at different concentration of ammonia ranging from 10 to 1500 ppm. The sensing response of the sensor was determined at 1500, 1000, 500, 200, 100 and 10 ppm and found to be 70.4, 66.1, 62.2, 55.4, 50.8 and 39.7%, respectively The sensor showed a complete reversibility at lower concentrations along with excellent selectivity and stability. Finally, a sensing mechanism was also proposed involving polarons (charge carriers) of polypyrrole and lone pairs of ammonia molecules

scholarly journals Synthesis of Propylene Carbonate from Epoxide and CO2 Catalyzed by Carbon Nanotubes Supported Fe1.5PMo12O40

2017 ◽  
Vol 2017 ◽  
pp. 1-9 ◽  
Author(s):  
Tahani Al-Garni ◽  
Nada Al-Jallal ◽  
Ahmed Aouissi
Keyword(s):  
Carbon Nanotubes ◽  
Propylene Carbonate ◽  
Inductively Coupled Plasma ◽  
Supported Catalyst ◽  
Catalyst Loading ◽  
X Ray Diffraction ◽  
Plasma Spectrometry ◽  
Inductively Coupled ◽  
Transmission Electron

Carbon nanotubes (CNTs) were functionalized and were then used as supports of Fe1.5PMo12O40 (FePMo) Keggin heteropolyanions catalysts. The characterization of the resulting catalysts was investigated by inductively coupled plasma spectrometry (ICP), Fourier transform infrared (FTIR) spectra, X-ray diffraction (XRD), ultraviolet-visible (UV-Vis) light spectroscopy, and transmission electron microscopy (TEM). FTIR and XRD results confirmed that FePMo was bounded on CNTs successfully and the Keggin structure was preserved. Characterization by TEM showed that solids with high FePMo content exhibited aggregation of FePMo in large particles. The as-prepared catalysts were tested in the synthesis of propylene carbonate (PC) from CO2 and propylene oxide (PO) in a solvent-free reaction and under mild conditions. Effects of various parameters, such as reaction temperature, reaction time, FePMo content on the support, and catalyst loading on the reaction, were investigated. It has been found that CNTs supported FePMo achieved 57.7% PO conversion and 99.0% PC selectivity, whereas unsupported FePMo led only to 8.5% conversion and 48.6% selectivity. The remarkable enhancement of the catalytic activity over the supported catalyst can be attributed mainly to the better dispersion and reactivity of the FePMo catalyst in the supported material.

Synthesis and Characterization of HgSe Nanostructure Using a Novel Precursor

2013 ◽  
Vol 32 (2) ◽  
pp. 157-162 ◽  
Author(s):  
Mahdiyeh Esmaeili-Zare ◽  
Masoud Salavati-Niasari ◽  
Davood Ghanbari
Keyword(s):  
Electron Microscopy ◽  
Synthesis And Characterization ◽  
Sonochemical Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Mercury Selenide ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

AbstractMercury selenide nanostructures were synthesized from the reaction of N, N′-bis(salicylidene)propane-1,3-diamine mercury complex, (Hg(Salpn)) as a novel precursor, via sonochemical method. The effect of different surfactant on the morphology and particle size of the products was investigated. Products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy and X-ray energy dispersive spectroscopy (EDS).

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