Preparation of Magnetic Surface-Imprinted Polymer Microspheres with Hydrophilic External Layers for Selective Extraction of Fluoroquinolones from Eggs

2017 ◽  
Vol 70 (3) ◽  
pp. 237 ◽  
Author(s):  
Yun-Kai Lv ◽  
Xue Xiong ◽  
Fang-Fang Zhao ◽  
Meng-Zhe Li ◽  
Mian Wang ◽  
...  
Keyword(s):  
Selective Extraction ◽  
Magnetic Surface ◽  
Magnetic Microspheres ◽  
Organic Polymer ◽  
One Pot ◽  
Transmission Electron ◽  
Ring Opening Reaction ◽  
Ft Ir ◽  
Novel Method ◽  
Ft Ir Spectroscopy

A novel method of one-pot covalently grafting a hydrophilic organic polymer imprinted layer on the surface of magnetic microspheres was developed for the preparation of restricted access materials–molecularly imprinted magnetic microspheres (RAM-MIMMs) with water compatibility and ability to exclude biomacromolecules and selectively enrich analytes. The magnetic nanoparticles were coated with silica gel, modified with vinyl groups, polymerized with the template (enrofloxacin), functional monomer (glycidyl methacrylate, methacrylic acid), and cross-linking agent (ethylene glycol dimethacrylate) in chloroform, and then the hydrophilic surface was formed by a ring-opening reaction. The RAM-MIMMs were characterized by transmission electron microscopy, FT-IR spectroscopy, and adsorption experiments and demonstrated average diameters around 400 nm and a coating thickness in the range of 50 nm. They exhibited high selectivity of the imprinted cavities and hydrophilicity of the external surface with water compatibility and exclusion of biomacromolecules. The RAM-MIMMs were used for the magnetic dispersion microextraction of fluoroquinolones from egg samples with satisfactory results.

Superoxide Anion Biosensor Based on Bionic-Enzyme Hyperbranched Polyester Particles

2018 ◽  
Vol 71 (3) ◽  
pp. 119
Author(s):  
Yanlian Niu ◽  
Sisheng Hu ◽  
Qian Zhou ◽  
Yang Liu ◽  
Yuhong Liu ◽  
...  
Keyword(s):  
Self Assembly ◽  
Hyperbranched Polyester ◽  
Manganese Phosphate ◽  
Transmission Electron ◽  
O2 Concentration ◽  
Ft Ir ◽  
Novel Method ◽  
Assembly Technology ◽  
Ft Ir Spectroscopy ◽  
Hyperbranched Structure

Self-assembly techniques have been demonstrated to be a useful approach to developing new functional nanomaterials. In this study, a novel method to fabricate a manganese phosphate self-assembly monolayer (SAM) on a hyperbranched polyester (HBPE-OH) nanoparticle surface is described. First, the second-generation aliphatic HBPE-OH was carboxy-terminated, phosphorylated, and then ionized with manganese by a three-step modification process. The final product of HBPE-AMPA-Mn2+ particles was obtained and characterised by FT-IR spectroscopy, 1H NMR spectroscopy, transmission electron microscopy (TEM), Zeta potential, and energy dispersive spectroscopy (EDS). Moreover, the HBPE-AMPA-Mn2+ particles were used to construct a novel biosensor for detection of superoxide anions (O2•−) released from HeLa cells. Results showed that the response currents of this biosensor were proportional to the O2•− concentration ranging from 0.79 to 16.6 μM, and provided an extremely low detection limit of 0.026 μM (S/N = 3). The results indicate that the particle-decorated electrode surface, which involved a hyperbranched structure and a surface self-assembly technology, proposed here will offer the ideal catalytic system for electrochemical enzymatic sensors.

Formation of Sic, Si3N4 and SiO2 by High-Dose Ion Implantation and Laser Annealing

1980 ◽  
Vol 1 ◽  
Author(s):  
S.W. Chiang ◽  
Y.S. Liu ◽  
R.F. Reihl
Keyword(s):  
Ion Implantation ◽  
Polycrystalline Silicon ◽  
Laser Annealing ◽  
Pulsed Laser ◽  
High Dose ◽  
Pulsed Laser Annealing ◽  
Transmission Electron ◽  
A Cell ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

ABSTRACTHigh-dose ion implantation (1017 ions-cm−2) of C+, N+, and O+ at 50 KeV into silicon followed by pulsed laser annealing at 1.06 μm was studied. Formation of SiC, Si3N4, and SiO2 has been observed and investigated using Transmission Electron Microscopy (TEM) and Differential Fourier-Transform Infrared (FT-IR) Spectroscopy. Furthermore, in N+-implanted and laser-annealed silicon samples, we have observed a cell-like structure which has been identified to be spheroidal polycrystalline silicon formed by the rapid laser irradiation.

Study on Nano- and Microcrystallites in Urines of Uric Acid Stone Patients

2013 ◽  
Vol 655-657 ◽  
pp. 1927-1930 ◽  
Author(s):  
Guang Na Zhang ◽  
Zhi Yue Xia ◽  
Jian Ming Ouyang ◽  
Li Kuan
Keyword(s):  
Electron Microscopy ◽  
Uric Acid ◽  
X Ray Diffraction ◽  
Uric Acid Stone ◽  
Urine Ph ◽  
Stone Formers ◽  
Transmission Electron ◽  
Close Relationship ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

The presence of crystallites in urine is closely related to stones formation. In this article, the components, morphology of nano- and micro-crystallites in urines of 20 uric acid (UA) stone formers as well as their relationship with the formation of UAstones were comparatively studied using X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The main constituent of urinary crystallites was uric acid. Their particle size distribution was highly uneven, ranging from several nanometers to several tens of micrometers, and obvious aggregation was observed. These results showed that there was close relationship among stone components, urinary crystallites composition and urine pH.

An expeditious one-pot synthesis of pyrido[2,3-d]pyrimidines using Fe3O4–ZnO–NH2–PW12O40 nanocatalyst

2019 ◽  
Vol 43 (3-4) ◽  
pp. 135-139
Author(s):  
Pegah Farokhian ◽  
Manouchehr Mamaghani ◽  
Nosrat Ollah Mahmoodi ◽  
Khalil Tabatabaeian ◽  
Abdollah Fallah Shojaie
Keyword(s):  
Electron Microscopy ◽  
Vibrating Sample Magnetometer ◽  
X Ray Diffraction ◽  
Facile Synthesis ◽  
Pyrimidine Derivatives ◽  
One Pot ◽  
X Ray ◽  
Transmission Electron ◽  
Novel Method ◽  
Operational Simplicity

An efficient protocol for the facile synthesis of a series of pyrido[2,3- d]pyrimidine derivatives has been developed applying Fe3O4–ZnO–NH2–PW12O40 nanocatalyst in water. This novel method has the benefits of operational simplicity, green aspects by avoiding toxic solvents and high to excellent yields of products. Fe3O4–ZnO–NH2–PW12O40 was synthesized and characterized by Fourier transform infrared, X-ray diffraction, vibrating sample magnetometer, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and transmission electron microscopy analyses. The nanocatalyst is readily isolated and recovered from the reaction mixture by an external magnet.

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 Green Synthesis of Carbon Dots from Grapefruit and Its Fluorescence Enhancement

2020 ◽  
Vol 2020 ◽  
pp. 1-7
Author(s):  
Xinzhu Huo ◽  
Yuxuan He ◽  
Shiqi Ma ◽  
Yingying Jia ◽  
Jiaming Yu ◽  
...  
Keyword(s):  
Carbon Dots ◽  
Carbon Sources ◽  
Carbon Quantum Dots ◽  
One Pot ◽  
Transmission Electron ◽  
Three Samples ◽  
Structure Morphology ◽  
Ir Transmission ◽  
Ft Ir ◽  
Doped Carbon Dots

In this study, undoped carbon quantum dots (UCQDs, UCQDs-peel) and N-doped carbon dots (NCQDs) were prepared by a facile one-pot environmentally friendly hydrothermal method using grapefruit as carbon sources in the absence and presence of area, respectively. The structure, morphology, and fluorescence properties of three samples were characterized by Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), and photoluminescence (PL). It was found that three types of CQDs could emit blue fluorescence with different intensities when irradiated with ultraviolet light. Compared to the luminescence properties of UCQDs, NCQDs, and UCQDs-peel, it can be seen that the fluorescence intensity of NCQDs was strongest due to the presence of NH and C-N bonds.

scholarly journals In Situ IR Characterization of CO Interacting with Rh Nanoparticles Obtained by Calcination and Reduction of Hydrotalcite-Type Precursors

2011 ◽  
Vol 2011 ◽  
pp. 1-8 ◽  
Author(s):  
F. Basile ◽  
I. Bersani ◽  
P. Del Gallo ◽  
S. Fiorilli ◽  
G. Fornasari ◽  
...  
Keyword(s):  
Crystal Size ◽  
Liquid Nitrogen Temperature ◽  
Transmission Electron ◽  
In Situ Ir ◽  
Ft Ir ◽  
Co Disproportionation ◽  
Ft Ir Spectroscopy

Supported Rh nanoparticles obtained by reduction in hydrogen of severely calcined Rh/Mg/Al hydrotalcite-type (HT) phases have been characterized by FT-IR spectroscopy of adsorbed CO [both at room temperature (r.t.) and nominal liquid nitrogen temperature] and Transmission Electron Microscopy (TEM). The effect of reducing temperature has been investigated, showing that Rh crystal size increases from 1.4 nm to 1.8 nm when the reduction temperature increases from 750°C to 950°C. The crystal growth favours the formation of bridged CO species and linear monocarbonyl species with respect to gem-dicarbonyl species; when CO adsorbs at r.t., CO disproportionation occurs on Rh and it accompanies the formation of RhI(CO)2. The role of interlayer anions in the HT precursors to affect the properties of the final materials has been also investigated considering samples prepared from silicate-instead of carbonate-containing precursors. In this case, formation of RhI(CO)2 and CO disproportionation do not occur, and this evidence is discussed in terms of support effect.

Synthesis of Fe 3+-Dopped PANI Conductive Nanomaterials via Interfacial Polymerization

2011 ◽  
Vol 239-242 ◽  
pp. 2839-2842
Author(s):  
Hong Mei Mu ◽  
Peng Fei ◽  
Bi Tao Su ◽  
Zi Qiang Lei
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fourier Transform ◽  
Ir Spectroscopy ◽  
Interfacial Polymerization ◽  
X Ray ◽  
Transmission Electron ◽  
Ft Ir ◽  
Conductive Nanomaterials ◽  
Ft Ir Spectroscopy

A series of Fe3+-dopped polyaniline (Fe3+/PANI) nanomaterials with different morphologies and a higher conductivity were successfully synthesized using a simple and static interfacial polymerization by using FeCl3 as both oxidant catalyst and dopant. The effect of surfactants CTAB and SDS and the concentration of FeCl3 on the morphology and conductivity of Fe3+/PANI nanomaterial were investigated. The samples were characterized by Transmission Electron Microscopy (TEM), SDY-4 probes conductivity meter, X-ray Diffractometry (XRD), Energy dispersive spectroscopy (EDS) and Fourier transform infrared (FT-IR) spectroscopy techniques. TEM’s results showed that their morphologies changed with the type of the surfactant and the concentration of FeCl3. Introducing surfactants CTAB and SDS into Fe3+/PANI remarkably improved the conductivity of the material. The conductivities of CTAB/Fe3+/PANI and SDS /Fe3+/PANI nanomaterials were respectively about 4.8×10-2 and 1.3×10-2 S/cm while the conductivity of Fe3+/PANI was found to be 1.5×10-4 S/cm. The different morphology and high conductivity may be ascribed to the mutual effects of the surfactant and oxidant.

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).

scholarly journals Preparation and characterization of highly blue emitting fluorescent carbon nano-dots using Pongammia pinnata fresh leaves

2021 ◽  
Author(s):  
Govindaraju K ◽  
K. Vijai Anand ◽  
S. Muthamilselvan ◽  
M. Kannan ◽  
M. Elanchezhiyan
Keyword(s):  
Electron Microscopy ◽  
Water Soluble ◽  
Hydrothermal Technique ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Ft Ir ◽  
Average Size ◽  
Soluble Carbon ◽  
Ft Ir Spectroscopy

Abstract In this study, a simple environmental benign approach have been adopted for the preparation of highly luminescent (blue emitting) water soluble carbon nano-dots using Pongammia pinnata (Pp) leaves via hydrothermal technique. The prepared Pp-carbon nano- dots were characterized using UV-vis spectroscopy, fluorescence spectroscopy, Fourier transform infrared (FT-IR) spectroscopy, transmission electron microscopy (TEM) and dynamic light scattering (DLS) measurements. The Pp-carbon nano-dots are spherical in shape with an average size of 32 nm.

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