scholarly journals Fabrication of Novel and Potential Selective 4-Cyanophenol Chemical Sensor Probe Based on Cu-Doped Gd2O3 Nanofiber Materials Modified PEDOT:PSS Polymer Mixtures with Au/µ-Chip for Effective Monitoring of Environmental Contaminants from Various Water Samples

Polymers ◽  
2021 ◽  
Vol 13 (19) ◽  
pp. 3379
Author(s):  
Mohammed Muzibur Rahman ◽  
S. Y. Alfaifi
Keyword(s):  
Chemical Sensor ◽  
Dynamic Range ◽  
Fast Response ◽  
Polymer Mixtures ◽  
X Ray Diffraction ◽  
Limit Of Quantification ◽  
Wide Linear Dynamic Range ◽  
Sensor Probe ◽  
Excellent Reproducibility

Herein, a novel copper-doped gadolinium oxide (Cu-doped Gd2O3; CGO) nanofiber was synthesized by a simple solution method in the basic phase and successfully characterized. We have used Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD), Field Emission Scanning Electron Microscope (FESEM) and Energy-Dispersive Spectroscopy (EDS) techniques for characterization of the CGO nanofiber. The CGO nanofiber was used later to modify Au-coated μ-Chips with poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) polymer mixtures (coating binder) to selectively detect 4-cyanophenol (4-CP) in an aqueous medium. Notable sensing performance was achieved with excellent sensitivity (2.4214 µAµM−1 cm−2), fast response time (~12 s), wide linear dynamic range (LDR = 1.0 nM–1.0 mM: R2 = 0.9992), ultra-low detection limit (LoD; 1.3 ± 0.1 pM at S/N = 3), limit of quantification (LoQ; 4.33 pM), and excellent reproducibility and repeatability for CGO/Au/μ-Chip sensor. This CGO modified Au/μ-chip was further applied with appropriate quantification and determination results in real environmental sample analyses.

One-step wet-chemical synthesis of ternary ZnO/CuO/Co3O4 nanoparticles for sensitive and selective melamine sensor development

2019 ◽  
Vol 43 (12) ◽  
pp. 4849-4858 ◽  
Author(s):  
M. M. Alam ◽  
Abdullah M. Asiri ◽  
M. T. Uddin ◽  
Inamuddin Inamuddin ◽  
M. A. Islam ◽  
...  
Keyword(s):  
Chemical Sensor ◽  
Dynamic Range ◽  
Fast Response ◽  
Co3o4 Nanoparticles ◽  
Linear Dynamic Range ◽  
Wet Chemical Synthesis ◽  
Electrochemical Approach ◽  
One Step ◽  
Wet Chemical ◽  
Sensor Probe

Using one-step wet-chemically synthesized ternary ZnO/CuO/Co3O4 nanoparticles (NPs) fabricated GCE sensor probe, a selective and sensitive melamine chemical sensor was developed by electrochemical approach, which exhibited the highest sensitivity, better repeatability, broad linear dynamic range, good linearity, fast response time, and lowest detection limit.

High Speed Characterization of Pseudomorphic Hemt Structures Using a Very Low Noise Scintillation Detector

1993 ◽  
Vol 37 ◽  
pp. 145-151
Author(s):  
N. Loxley ◽  
S. Cockerton ◽  
B. K. Tanner
Keyword(s):  
Quality Assurance ◽  
Scintillation Detector ◽  
High Speed ◽  
Dynamic Range ◽  
High Dynamic Range ◽  
Low Noise ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Dynamic

AbstractWe show that a very low noise, high dynamic range scintillation detector has major advantages over conventional detectors for characterization of pseudomorphic HEMT structures by high resolution X-ray diffraction. We show that the reduced background enables a second modulation period to be detected, enabling the thickness and composition to be determined independently. Using a conventional X-ray generator and diffractometer we demonstrate that, in a single scan taking only 10 seconds, we are able to obtain sufficiently good data to provide quality assurance.

scholarly journals A Large-Scale Synthesis and Characterization of QuaternaryCuInxGa1−xS2Chalcopyrite Nanoparticles via Microwave Batch Reactions

2011 ◽  
Vol 2011 ◽  
pp. 1-8 ◽  
Author(s):  
Chivin Sun ◽  
Richard D. Westover ◽  
Gary Long ◽  
Cyril Bajracharya ◽  
Jerry D. Harris ◽  
...  
Keyword(s):  
Large Scale ◽  
Size Composition ◽  
Nanoparticle Size ◽  
Synthesis And Characterization ◽  
Icp Oes ◽  
X Ray Diffraction ◽  
High Reproducibility ◽  
X Ray ◽  
Excellent Reproducibility

Various quaternaryCuInxGa1−xS2(0≤x≤1) chalcopyrite nanoparticles have been prepared from molecular single-source precursors via microwave decomposition. We were able to control the nanoparticle size, phase, stoichiometry, and solubility. Depending on the choice of surface modifiers used, we were able to tune the solubility of the resulting nanoparticles. This method has been used to generate up to 5 g of nanoparticles and up to 150 g from multiple batch reactions with excellent reproducibility. Data from UV-Vis, photoluminescence, X-ray diffraction, TEM, DSC/TGA-MS, and ICP-OES analyses have shown high reproducibility in nanoparticle size, composition, and bandgap.

Comparative performances of phenolic sensors based on various CeO2-carbon material nanocomposites for environmental safety

Sensor Review ◽  
2018 ◽  
Vol 38 (4) ◽  
pp. 467-477 ◽  
Author(s):  
Faisal K. Algethami ◽  
Hadi M. Marwani ◽  
Abdullah M. Asiri ◽  
Mohammed M. Rahman
Keyword(s):  
Detection Limit ◽  
Carbon Material ◽  
Chemical Sensor ◽  
Ultra Violet ◽  
Limit Of Quantification ◽  
Content Type ◽  
Electrochemical Approach ◽  
Vis Spectroscopy ◽  
Wet Chemical ◽  
Sensor Probe

Purpose The purpose of this study is to prepare various CeO2-based carbon material (CNT, CB, GO) nanocomposites through a wet chemical process for the development of a sensor probe to detect various environmental toxins by using an electrochemical approach under room temperature conditions. A comparative study on sensitive and selective phenolic sensor (4-methoxyphenol; 4-MP) has been fabricated by modifying a glassy carbon electrode (GCE) with various nanocomposites (NCs) such as CeO2, CeO2–CNT (carbon nanotubes), CeO2–CB (carbon black) and CeO2–GO (graphene oxide) NCs. Design/methodology/approach The CeO2–CNT NCs were prepared by the wet chemical method at low temperature. NCs were characterized by various methods such as transmission electron microscopy (TEM), Fourier-transform infra-red (FTIR), ultra-violet/visible (UV-Vis) spectroscopy and XRD (X-ray diffraction). CeO2–CNT NCs were immobilized as a film on the flat surface of the GCE by using binders (5% Nafion). The electrochemical measurements of the 4-MP detection with the CeO2–CNT NCs/Nafion/GCE sensor were studied by the current-voltage method. Findings In the optimal conditions, the sensitivity, detection limit and limit of quantification of 4-MP sensor probe were found to be 47.56 µAcm-2 µM−1, 12.0 ± 0.2 nM and 40.0 ± 0.5 nM (S/N of 3), respectively. Research limitations/implications This electrochemical sensor showed an acceptable analytical performance in the detection of 4-MP with higher sensitivity, lower detection limit, large dynamic concentration range, good reproducibility and fast response time. Practical implications This electrochemical approach can be applied practically for the determination of selective 4-MP in real environmental and extracted samples. Social implications CeO2–CNT NCs/Nafion/GCE sensor probe was used for the safety of environmental and health-care fields at larger scales. Originality/value This electrochemical approach is a significant achievement on the development of sensor probe. The results are indicated as being technically detailed with an up-to-date account of recent chemical sensor research studies.

scholarly journals Rapid and sensitive detection of selective 1,2-diaminobenzene based on facile hydrothermally prepared doped Co3O4/Yb2O3 nanoparticles

PLoS ONE ◽  
2021 ◽  
Vol 16 (2) ◽  
pp. e0246756
Author(s):  
Mohammed M. Rahman
Keyword(s):  
Chemical Sensor ◽  
Dynamic Range ◽  
Electrochemical Technique ◽  
Carbon Electrode ◽  
Linear Dynamic Range ◽  
Linear Dynamic ◽  
Low Dimensional ◽  
Sensor Probe ◽  
Broad Scale

In this approach, the performance of a newly developed sensor probe coated with low-dimensional Co3O4/Yb2O3 nanoparticles (NPs) in rapidly detecting 1,2-diaminobenzene was evaluated by an electrochemical technique. The sensor probe was fabricated by depositing a very thin layer consisting of synthesized Co3O4/Yb2O3 NPs using a 5% Nafion conducting binder onto a glassy carbon electrode (GCE). The facile hydrothermally prepared Co3O4/Yb2O3 NPs were totally characterized by conventional methods such as FTIR, UV-vis, TEM, XPS, EDS, and XRD analyses. The fabricated chemical sensor probe was found to exhibit long-term activity, stability in electrochemical response, good sensitivity (5.6962 μAμM-1cm-2), lowest detection limit (0.02±0.001 pM), and broad linear dynamic range (0.1 pM to 0.01 mM). The observed performances suggest that the newly introduced sensor could play an efficient role in detecting 1,2-diaminobenzene especially in healthcare and environmental applications on a broad scale.

The Use of Advanced Analytical Techniques for Characterization of the Chemical, Physical, and Crystallographic Nature of a Surface

1973 ◽  
Vol 31 ◽  
pp. 132-133 ◽  
Author(s):  
R. E. Herfert
Keyword(s):  
Surface Characterization ◽  
Analytical Techniques ◽  
X Ray Diffraction ◽  
Depth Of Penetration ◽  
X Ray ◽  
The Past ◽  
Transmission Electron ◽  
Scanning Electron

Studies of the nature of a surface, either metallic or nonmetallic, in the past, have been limited to the instrumentation available for these measurements. In the past, optical microscopy, replica transmission electron microscopy, electron or X-ray diffraction and optical or X-ray spectroscopy have provided the means of surface characterization. Actually, some of these techniques are not purely surface; the depth of penetration may be a few thousands of an inch. Within the last five years, instrumentation has been made available which now makes it practical for use to study the outer few 100A of layers and characterize it completely from a chemical, physical, and crystallographic standpoint. The scanning electron microscope (SEM) provides a means of viewing the surface of a material in situ to magnifications as high as 250,000X.

High Resolution Replication of Organoclay Surfaces

1982 ◽  
Vol 40 ◽  
pp. 576-577
Author(s):  
W. W. Barker ◽  
W. E. Rigsby ◽  
V. J. Hurst ◽  
W. J. Humphreys
Keyword(s):  
Clay Mineral ◽  
Organic Molecule ◽  
Organic Molecules ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Naturally Occurring ◽  
Silicate Layers ◽  
Mineral Identification

Experimental clay mineral-organic molecule complexes long have been known and some of them have been extensively studied by X-ray diffraction methods. The organic molecules are adsorbed onto the surfaces of the clay minerals, or intercalated between the silicate layers. Natural organo-clays also are widely recognized but generally have not been well characterized. Widely used techniques for clay mineral identification involve treatment of the sample with H2 O2 or other oxidant to destroy any associated organics. This generally simplifies and intensifies the XRD pattern of the clay residue, but helps little with the characterization of the original organoclay. Adequate techniques for the direct observation of synthetic and naturally occurring organoclays are yet to be developed.

Quantitative Electron Microscope with imaging plate

1994 ◽  
Vol 52 ◽  
pp. 408-409
Author(s):  
D. Shindo
Keyword(s):  
Electron Microscope ◽  
Dynamic Range ◽  
Processing System ◽  
Digital Data ◽  
Imaging Plate ◽  
Crystal Thickness ◽  
X Ray Diffraction ◽  
Resolution Electron ◽  
Electron Intensity ◽  
Diffraction Patterns

Imaging plate has good properties, i.e., a wide dynamic range and good linearity for the electron intensity. Thus the digital data (2048x1536 pixels, 4096 gray levels in log scale) obtained with the imaging plate can be used for quantification in electron microscopy. By using the image processing system (PIXsysTEM) combined with a main frame (ACOS3900), quantitative analysis of electron diffraction patterns and high-resolution electron microscope (HREM) images has been successfully carried out.In the analysis of HREM images observed with the imaging plate, quantitative comparison between observed intensity and calculated intensity can be carried out by taking into account the experimental parameters such as crystal thickness and defocus value. An example of HREM images of quenched Tl2Ba2Cu1Oy (Tc = 70K) observed with the imaging plate is shown in Figs. 1(b) - (d) comparing with a structure model proposed by x-ray diffraction study of Fig. 1 (a). The image was observed with a JEM-4000EX electron microscope (Cs =1.0 mm).

Synthesis and characterization of TiN / Ti / AISI 410 coatings

2018 ◽  
Vol 2 (1) ◽  
pp. 7
Author(s):  
S Chirino ◽  
Jaime Diaz ◽  
N Monteblanco ◽  
E Valderrama
Keyword(s):  
Synthesis And Characterization ◽  
Photoemission Spectroscopy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Columnar Grains ◽  
Tin Thin Films ◽  
Steel Aisi ◽  
Interacting Surfaces ◽  
Stainless Steel Aisi

The synthesis and characterization of Ti and TiN thin films of different thicknesses was carried out on a martensitic stainless steel AISI 410 substrate used for tool manufacturing. The mechanical parameters between the interacting surfaces such as thickness, adhesion and hardness were measured. By means of the scanning electron microscope (SEM) the superficial morphology of the Ti/TiN interface was observed, finding that the growth was of columnar grains and by means of EDAX the existence of titanium was verified.  Using X-ray diffraction (XRD) it was possible to observe the presence of residual stresses (~ -3.1 GPa) due to the different crystalline phases in the coating. Under X-ray photoemission spectroscopy (XPS) it was possible to observe the molecular chemical composition of the coating surface, being Ti-N, Ti-N-O and Ti-O the predominant ones.

Glibenclamide-Nicotinamide Cocrystals Synthesized by The Solvent Evaporation Method to Enhance Solubility and Dissolution Rate of Glibenclamide

2019 ◽  
Vol 9 (01) ◽  
pp. 21-26
Author(s):  
Arif Budiman ◽  
Ayu Apriliani ◽  
Tazyinul Qoriah ◽  
Sandra Megantara
Keyword(s):  
Solvent Evaporation ◽  
Physical Mixture ◽  
Dissolution Profile ◽  
Solvent Evaporation Method ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Evaporation Method ◽  
Dissolution Properties ◽  
Mixture Characterization

Purpose: To develop glibenclamide-nicotinamide cocrystals with the solvent evaporation method and evaluate their solubility and dissolution properties. Methods: Cocrystals of glibenclamide-nicotinamide (1:2) were prepared with the solvent evaporation method. The prediction of interactive cocrystals was observed using in silico method. The solubility and dissolution were performed as evaluation of cocrystals. The cocrystals also were characterized by differential scanning calorimetry (DSC), infrared spectrophotometry, and powder X-ray diffraction (PXRD). Result: The solubility and dissolution profile of glibenclamide-nicotinamide cocrystal (1:2) increased significantly compared to pure glibenclamide as well as its physical mixture. Characterization of cocrystal glibenclamide-nicotinamide (1:2) including infrared Fourier transform, DSC, and PXRD, indicated the formation of a new solid crystal phase differing from glibenclamide and nicotinamide. Conclusion: The confirmation of cocrystal glibenclamide-nicotinamide (1:2) indicated the formation of new solid crystalline phases that differ from pure glibenclamide and its physical mixture

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