In this work, several attempts were made to prepare nanoceramic zirconate (Nd₂Zr₂O7) powder for pigment applications. The single pyrochlore phase, Nd₂Zr₂O7 was successfully synthesized with the aid of flux at relatively low temperature (1000 °C) upon milling the reaction mixture made from Nd₂O₃ and ZrO₂ in a tungsten carbide vial. Several characterizations were done on the thermal analysis (TG/DTA), X-ray diffraction (XRD), High-resolution scanning electron microscope (HRSEM), energy dispersive X-ray (EDX) analysis, Fourier-transform infrared (FT-IR) analysis, and near-infrared (NIR spectroscopy). A single-phase nanocrystalline (˜28 nm) pyrochlore structure (Fd3m) was confirmed through XRD analysis. A highly uniform particle in the size of ˜110 nm was observed for the Nd₂Zr₂O7 phase in the microimages. The vibrational (FT-IR) peaks at 423 cm-1 and 510 cm-1 in FTIR spectroscopic study confirmed the formation of pyrochlore structure. Higher NIR reflectivity recorded for this material in the 750-2500 nm region shows its novel application in color cool pigments for energy-saving paints reminiscent of Bi2-xY x Ce²O7, Bi²Ce2-xTbxO7, and Gd²Ti²O7.Magnetic CoFe₂O₄ nanoparticles were successfully manufactured through the process of nitrate combustion using anhydrous ethanol as fuel, they together with their intermediate were characterized by thermo gravimetric (TG) analysis, selected area electron diffraction (SAED), transmission electron microscope (TEM), vibrating sample magnetometer (VSM), and X-ray diffraction (XRD). These results indicated a phenomenon that the magnetic CoFe₂O₄ nanoparticles could be formed at 400 °C, the average grain size, the specific magnetization, and the specific surface area of magnetic CoFe₂O₄ nanoparticles fabricated at 400 °C for 2 h with 30 mL anhydrous ethanol were corresponding 20 nm, 78.0 Am²/kg and 83.2 m²/kg. Magnetic CoFe₂O₄ nanoparticles were in application to adsorb methyl blue (MB) of wastewater, and their adsorption performances and electrochemical properties were investigated, the adsorption process data well agreed with the pseudo-second-order kinetics model in concentration ranging from 100 mg/L to 400 mg/L of MB. Compared with Freundlich model, Langmuir model (correlation coefficient R² = 0.9976) could evaluate the adsorption equilibrium state of MB onto CoFe₂O₄ nanoparticles at indoor temperature, so the monomolecular layer adsorption mechanism was demonstrated to be the mechanism of the MB molecules' adsorption onto CoFe₂O₄ nanoparticles.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. 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. https://www.selleckchem.com/products/AT7867.html 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.
In this work, several attempts were made to prepare nanoceramic zirconate (Nd₂Zr₂O7) powder for pigment applications. The single pyrochlore phase, Nd₂Zr₂O7 was successfully synthesized with the aid of flux at relatively low temperature (1000 °C) upon milling the reaction mixture made from Nd₂O₃ and ZrO₂ in a tungsten carbide vial. Several characterizations were done on the thermal analysis (TG/DTA), X-ray diffraction (XRD), High-resolution scanning electron microscope (HRSEM), energy dispersive X-ray (EDX) analysis, Fourier-transform infrared (FT-IR) analysis, and near-infrared (NIR spectroscopy). A single-phase nanocrystalline (˜28 nm) pyrochlore structure (Fd3m) was confirmed through XRD analysis. A highly uniform particle in the size of ˜110 nm was observed for the Nd₂Zr₂O7 phase in the microimages. The vibrational (FT-IR) peaks at 423 cm-1 and 510 cm-1 in FTIR spectroscopic study confirmed the formation of pyrochlore structure. Higher NIR reflectivity recorded for this material in the 750-2500 nm region shows its novel application in color cool pigments for energy-saving paints reminiscent of Bi2-xY x Ce²O7, Bi²Ce2-xTbxO7, and Gd²Ti²O7.Magnetic CoFe₂O₄ nanoparticles were successfully manufactured through the process of nitrate combustion using anhydrous ethanol as fuel, they together with their intermediate were characterized by thermo gravimetric (TG) analysis, selected area electron diffraction (SAED), transmission electron microscope (TEM), vibrating sample magnetometer (VSM), and X-ray diffraction (XRD). These results indicated a phenomenon that the magnetic CoFe₂O₄ nanoparticles could be formed at 400 °C, the average grain size, the specific magnetization, and the specific surface area of magnetic CoFe₂O₄ nanoparticles fabricated at 400 °C for 2 h with 30 mL anhydrous ethanol were corresponding 20 nm, 78.0 Am²/kg and 83.2 m²/kg. Magnetic CoFe₂O₄ nanoparticles were in application to adsorb methyl blue (MB) of wastewater, and their adsorption performances and electrochemical properties were investigated, the adsorption process data well agreed with the pseudo-second-order kinetics model in concentration ranging from 100 mg/L to 400 mg/L of MB. Compared with Freundlich model, Langmuir model (correlation coefficient R² = 0.9976) could evaluate the adsorption equilibrium state of MB onto CoFe₂O₄ nanoparticles at indoor temperature, so the monomolecular layer adsorption mechanism was demonstrated to be the mechanism of the MB molecules' adsorption onto CoFe₂O₄ nanoparticles.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. 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. https://www.selleckchem.com/products/AT7867.html 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.
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