Notes

Semi-batch along with constant manufacture of Pickering emulsion by way of immediate speak to water cumul.
ZrC was produced by the combustion synthesis technology using Cu, Zr, and graphite as the starting element powders. The synthesis mechanism of ZrC was investigated by the combustion wave quenching experiment. Furthermore, the effects of sizes of C and Cu on the combustion synthesis behavior and products were also explored. Results revealed that ZrC was fabricated through the displacement reaction between C and Cu-Zr liquid. The Cu size hardly affected the combustion temperature and resultant products, indicating that the preparation cost of ZrC could be decreased by employing coarse Cu powders. With increasing C size, the burning temperature and ceramic particle size reduced. Graphite with size of 2.6 μm was used as the C source, and only ZrC nanoparticles and Cu were obtained. The products could be employed to prepare nano-sized ZrC/Cu composites without the elimination of by-products.The present work describes the preparation and the investigation of the room temperature electrical and optical properties of a series of liquid nanocomposites (lnC) prepared with different concentrations of multiwalled carbon nanotubes (MWCNT) in a variety of liquid matrices glycerin, Vaseline, glucose, propylene glycol and silicone oil (SIO). Special attention is deserved to the SIO matrix, owing to its convenient electrical properties for our purposes. We verified that a small percent fraction of MWCNT dispersed along the SIO matrix is capable of improving the electrical conductivity of the matrix by orders of magnitude, indicating that the MWCNT strongly participates in the electrical conduction mechanism. Also, the application of an external electric field to this lnC resulted in large changes in the optical transmittance, that were interpreted as a consequence of the fieldinduced MWCNT alignment into the liquid matrix. The characteristics of such a new category of nanocomposite in the liquid state suggest further studies.Polylactide-b-poly(N-isopropylacrylamide)-b-polystyrene (PLA-b-PNIPAM-b-PS) triblock copolymers (tri-BCPs) with various chemical compositions (block ratio) were prepared from the combination of ring-opening polymerization and reversible addition-fragmentation chain transfer polymerization. PRT543 Subsequently, the self-assembling behaviors of these tri-BCP films obtained from spin-coating were investigated by annealing them under different solvent atmosphere. We found that these films could self-assemble into various morphologies due to the microphase separation of incompatible copolymer blocks. Atomic force microscopy confirmed the perpendicular cylindrical morphology self-assembled from PLA4.5k-b-PNIPAM5.2k-b-PS22.4k tri-BCP film under mixed solvent atmosphere of toluene/acetone (73, v/v). Self-assembled PLA cylinders are evenly distributed among the PS matrix and perpendicular to the film surface, with PNIPAM component taking place at the PLA/PS interphase. Furthermore, by etching the degradable PLA component, porous PS film decorated with PNIPAM "brushes" hoisting channels were generated. This work provides a facile method and detailed protocol for fabricating stimuli-responsive porous films which are promising for thermoresponsive "smart" separation technologies.In this study, we evaluate the defects and charges caused by the ultraviolet (UV)/vacuum ultraviolet (VUV) irradiation in the high-k/metal gate stack structure, especially in HfO₂ layer and at Si/HfO₂ interface. First, we measured the photons irradiating to the surface in the neutral beam etching (NBE) system and in the conventional inductively coupled plasma (ICP) system through optical emission spectroscopy (OES), respectively. By using this method, we evaluate the ability of reducing UV/VUV irradiation damage in the NBE system. As a result, photon intensity detected in the ICP system shows larger magnitude as compared to the NBE system, which indicates the UV/VUV irradiation is more severe in the ICP system. Moreover, in order to understand the twisting of electrical characteristics caused by UV/VUV irradiation, we set the prefabricated metal-oxide-semiconductor (MOS) capacitors in both systems to absorb the irradiation of UV/VUV photons respectively. The electrical characteristics of the etched MOS capacitors and its related plasma-induced damage model are discussed. The result of the devices exposed in the ICP system reveals a greater electrical characteristics shift compared to the devices in NBE such as the interface trap density (Dit) in case of NBE is 3.55621×1012 cm-2eV-1 and in case of ICP is higher i.e., 4.19961×1012 cm-2eV-1.Calcium copper titanate (CaCu₃Ti₄O12; CCTO) ceramics are useful as capacitor dielectrics for many applications. In this study the effect of doping with alumina and testing atmospheres in air and dry N₂ on the stability and reproducibility of electrical and dielectric properties of CCTO-xAl₂O₃ system, where x = 0, 0.5, and 4 wt.% as a function of temperature are investigated. Solid-state synthesis route is used to fabricate the pure and doped CCTO samples sintered at 1080 °C and 1100 °C for 5 h in air. Stable and reproducible dielectric properties are obtained only by switching the measuring atmosphere from air to dry N₂. Increased space charge accumulation at the grain boundaries leading to large dielectric constant (ε') and tan δ are measured in air. Much lower tan δ values of 0.021-0.020 are obtained with a large ε' (8,815-11,090) at low frequencies (500-800 Hz) in N₂ at 23 °C for 0.5 wt.% alumina in both samples sintered at 1080 °C and 1100 °C. These results clearly demonstrate that testing environment can dominate the dielectric properties of pure and alumina-doped CCTO at low frequencies unless measured in dry nitrogen atmosphere to achieve intrinsic behavior useful for applications as capacitors.SiCOH thin films were deposited on rigid silicon (Si) wafers and flexible ITO/PEN substrates via plasma-enhanced chemical vapor deposition at room temperature using a tetrakis(trimethylsilyloxy)silane (TTMSS) precursor. Different chemical compositions of hydrocarbon and Si-O bondings were obtained depending on substrate types and deposition conditions. The main chemical compositions of the as-deposited films were observed as C-H x (x = 2, 3) stretching, Si-CH₃ bending, Si-O-Si stretching, and H-Si-O bending/Si-CH₃ stretching modes. With regard to the as-deposited films, the dielectric constant increased from 1.83 to 3.45 when the plasma power increased from 20 to 80 W and the lowest leakage current of 1.76×10-4 A/cm² was obtained at the plasma power of 80 W. After bending tests with 1000, 5000, and 10000 bending cycles, the dielectric constants of the SiCOH films increased and leakage currents decreased. link2 The structures of the SiCOH films after the bending tests were highly complicated with a variety of chemical bonding combinations. Higher peak intensity and peak area of main chemical bonding were obtained with the increased bending cycles, resulting in the increase in dielectric constants. It should be noted that the film with small changes in peak area fractions of the bending and stretching modes showed good electrical and mechanical stabilities after bending tests.Industrialization can be greatly appreciated only by limiting the downside of the proposed technology. In this aeon, the recurrent monitoring of industries is statutory in detecting harmful gases and explosions for the global environment safety. Hence, employing specific gas sensors for detecting malicious gases benefits the welfare of the society. Thus, in this present work, we developed an energy efficient toxic gas sensor using ZnO thin film by seed layer assisted hydrothermal technique. The sensing mechanism of ZnO with the CO analyte was explained and the sensing parameters such as sensitivity, selectivity, response and recovery time were studied. Further, the developed energy efficient sensor was embedded with wireless sensor assembly for online monitoring which may be functional in developing portable, compact and cost-effective system for various real time industrial control applications.A simple, low-cost and highly selective nanosensor was developed for naked-eye detection of mercury ions (Hg2+) based on Eosin/silver nanocubes (Eosin/AgNCbs). link3 Silver nanocubes (AgNCbs) were synthesized by polyol assisted chemical method. HR-TEM result shows the formed AgNCbs have a mean diameter of 84±0.005 nM (diagonally measured) and edge length of 55±0.01 nM. XRD result confirms that the AgNCbs are single crystalline in nature with a phase structure of face centered cubic (FCC) of silver. On interaction of Hg2+, AgNCbs exhibits a color change from gray to black up to 16.67 μM of Hg2+ owed to the formation of solid like bimetallic complex of Ag/Hg amalgam. The selectivity of AgNCbs was evaluated with several other toxic metal ions including, Mg2+, Ba2+, Ca4+, Pb2+, Cd4+, Zn2+, Co2+, Cu2+, K+ and Ni2+ and found good selectivity towards Hg2+. The sensitivity of the AgNCbs sensor system was tuned by using Eosin as a co-staining agent. The Eosin/AgNCbs showed a limit of detection of 60±0.050 nM with the color change from orange to purple. The results suggests that the Eosin/AgNCbs nanosensor exhibits good selectivity, sensitivity, repeatability and rapid response, which could be explored for real-time detection of Hg2+ in environmental and biological samples.Heavy metal Cadmium (Cd) will continuously pollute the atmosphere, soil and various water environments through material circulation, and even pose a threat to human safety. It has been designated as a first-class pollutant in sewage by China, therefore there is an urgent need to find new, more effective, and low-cost method to accurately detect Cadmium ion (Cd2+) concentration. We experimentally prepared a new Cd2+ sensor based on NiS₂ nanomaterials capable of measuring Cd2+ concentration. The corresponding relationship between over potential of NiS₂ nanomaterials in H₂SO₄ electrolyte solutions with different Cd2+ concentration and reduction peak with change of Cd2+ concentration was obtained by electrochemical method.Due to the complexity of traditional Chinese medicines (TCMs), it is very important to develop a method that can recognize anthraquinones, the active ingredients in TCMs, with high selectivity. Here, a molecularly imprinted fluorescence sensor was coated on the surface of carbon quantum dots (CDs). Allobarbital was used as functional monomer for this application using theoretical calculations and was successfully synthesized and characterized. The template molecule chrysophanol was combined with the functional monomer allobarbital using a hydrogen bond array. Then, a series of adsorption experiments were performed to study the specific recognition of anthraquinones by the prepared sensors. The results showed that the prepared sensor had a good linear response to concentrations of chrysophanol in the concentration range 0.5 mg · L-1 to 8.0 mg · L-1, a low detection limit (5.0 μg · L-1), high stability, and a short response time (20 min). Additionally, the obtained fluorescence sensor was successfully applied to selectively recognize anthraquinones in TCMs with recoveries of 90.1% to 101.7%. The prepared sensor displays excellent sensitivity and high selectivity towards anthraquinones, mainly due to the specific hydrogen binding sites for the target molecules. Overall, this fluorescence sensor can selectively recognize anthraquinones in TCMs, and provide a method for quality monitoring and rational utilization of TCMs.
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