2,859 publications from this institution
A highly selective chemisensor for 2-nitrophenol detection was fabricated using ZnO/RuO<sub>2</sub> nanoparticles (NPs) synthesized by impregnation method. The as-synthesized NPs were characterized through UV-vis diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FESEM), Energy dispersive X-ray spectroscopy (EDS), FTIR and X-ray diffraction (XRD). A glassy carbon electrode was modified with as-synthesized ZnO/RuO<sub>2</sub> nanoparticles and utilized as a chemical sensor for the detection of 2-nitrophenol. The fabricated sensor exhibited excellent sensitivity (18.20 μA μM<sup>-1</sup> cm<sup>-2</sup>), good reproducibility, short response time (8.0 s.), the lowest detection limit (52.20 ± 2.60 pM) and long-term stability in aqueous phase without interference effects. Finally, the fabricated sensor was validated as a 2-NP probe in various environmental water samples at room conditions.
ABSTRACT Photoinduced free radical polymerization of vinyl monomers by using semiconductor inorganic nanoparticles (NPs) is investigated. Zinc oxide and iron‐doped zinc oxide were used as photosensitive compounds to initiate the polymerization of acrylamide as a water‐soluble monomer in aqueous environment and methyl methacrylate as an oil‐soluble monomer in organic media under UV‐light irradiation. The method uses photochemically generated electrons and holes from the NPs to form initiating hydroxyl radicals in aqueous media, while tertiary amines and iodonium salt served as coinitiator in organic media. The initiation mechanism in organic media involves hydrogen abstraction or reduction processes via charge carriers, respectively. The kinetic of the polymerization in both environments was studied by means of a photo‐differential scanning calorimetry. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52 , 1500–1507
In the title compound, C(15)H(13)NO(3)S, the benzene ring and the five-membered heterocyclic ring are oriented at a dihedral angle of 12.00 (6)°. In the crystal, C-H⋯O inter-actions generate two types of cyclic motifs, R(2) (2)(14) and R(2) (2)(26), connecting the mol-ecules into tapes extending along [101]. In addition, there are π-π stacking inter-actions between the benzene and thio-phene rings with centroid-centroid distances of 3.7263 (14) and 3.7487 (14) Å.
A CoP nanoarray behaves as a robust non-noble-metal recyclable catalyst for effective on-demand hydrogen generation from ammonia borane hydrolysis, with an initial turnover frequency and activation energy of 42.8 mol<sub>H2</sub> mol<sub>CoP</sub><sup>−1</sup> min<sup>−1</sup> and 34.1 kJ mol<sup>−1</sup>, respectively.
This book Electrochemical Sensors Technology mostly reviews the modem methods and significant electrochemical and electroanalytical applications of chemical sensors and biosensors. Chapters of this book are invited and contributed from the experts throughout the world from prominent researchers and scientists in the field of sensors and in the field of electro- and biochemistry. Each chapter provides technical and methodological details beyond the level found in typical journal articles or reviews and explores the application of chemical sensors, environmental sensors, and biosensors to a significant problem in biomedical and environmental science, also providing a prospectus for the future. This book compiles with the expert knowledge of many specialists in the construction and use of chemical sensors and biosensors including chemical sensors, biological sensors, DNA sensors, immunosensors, gaseous sensors, ionic sensors, bioassay sensors, lab-on-chips, devices, portable sensors, microchips, nanosensors, implantable microsensors, and so on in the field of fundamental and applied electrochemistry. Highlights and importance are laid on real or practical problems, ranging from chemical application to biomedical monitoring, from in vitro to in vivo, and from single cell to animal to human measurement. This offers a unique opportunity of exchanging and combining the scientist or researcher in electrochemical sensors in largely chemistry, biological engineering, electronic engineering, and biomedical and physiological fields.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
Herein, an easy wet-chemical process was used in basic medium with low temperature to prepare low-dimensional copper oxide nanoparticles (CuO NPs). A variety of optical and structural techniques such as UV-visible, FT-IR, XRD, FESEM, XEDS, and XPS were used to characterize the synthesized CuO NPs in detail. Two sensitive and selective sensor probes for γ-amino-butyric acid (GABA) and testosterone (TST) were achieved after modification; a thin layer of NPs on a flat glassy carbon electrode (GCE). Sensor analytical parameters such as sensitivity (SNT), linear dynamic range (LDR), limit of detection (LOD), limit of quantification (LOQ), robustness, and interference effects, were evaluated for the proposed sensor (GCE/CuO NPs) for GABA and TST, based on a dependable current-voltage technique. Calibration curves were found to be linear (<i>R</i> <sup>2</sup> = 0.9963 and 0.9095) over a broad concentration range of GABA and TST (100.0 pM to 100.0 mM and 10.0 pM to 10.0 mM, respectively). Sensor parameters - SNT (316.46 and 2848.10 pA μM<sup>-1</sup> cm<sup>-2</sup>), LDR (100.0 nM to 10.0 mM and 10.0 pM to 1.0 mM), LOD (≈11.70 and 96.67 pM), and LOQ (39.0 and 322.2 pM) - for GABA and TST were calculated from the calibration plot successively. Preparation of CuO NPs using the wet-chemical technique is a good approach for perspective expansion of NPs-based sensors for the enzyme-free detection of biomolecules. Our sensor probe (GCE/CuO NPs) is applied for the cautious recognition of GABA and TST in real biological samples -human, mouse, and rabbit serum - and achieved good and acceptable results.