Preparation and properties of nano-TiO2 modified interior wall paint

The modification of the traditional interior wall paint was carried out by means of adding nano-TiO2 as a functional pigment. By regulating the dosage of dispersant, the nano-particles can be dispersed in paint homogeneously. With two aspects of experiments： dosage of nano-TiO2 and pigment volume concentration （PVC）, the paint formulation can be optimized and its properties~ such as hardness, scrub resistance, storage stability, contrast ratio and gloss can be improved. Finally an interior wall paint with high performance and air purification was prepared. Its character of formaldehyde degradation would be discussed in the next article.

Nitridation of chromium powder in ammonia atmosphere

CrN powder was synthesized by nitriding Cr metal in ammonia gas flow, and its chemical reaction mechanism and nitridation process were studied. Through thermodynamic calculations, the Cr-N-O predominance diagrams were constructed for different tempera- tures. Chromium nitride formed at 700-1200℃ under relatively higher nitrogen and lower oxygen partial pressures. Phases in the products were then investigated using X-ray diffraction （XRD）, and the Cr2N content varied with reaction temperature and holding time. The results indicate that the Cr metal powder nitridation process can be explained by a diffusion model. Further, Cr2N formed as an intermediate product because of an incomplete reaction, which was observed by high-resolution transmission electron microscopy （HRTEM）. After nitriding at 1000℃ for 20 h, CrN powder with an average grain size of 63 nm was obtained, and the obtained sample was analyzed by using a scanning electron microscope （SEM）.

Fluorite Ce_(0.8)Sm_(0.2)O_(2-δ) porous layer coating to enhance the oxygen permeation behavior of a BaCo_(0.7)Fe_(0.2)Nb_(0.1)O_(3-δ) mixed conductor

Fluorite Ce0.8Sm0.2O2-δ（SDC） nanopowder with a crystallite size of 15 nm was synthesized by a co-precipitation method. An SDC porous layer was coated onto a BaCo0.7Fe0.2Nb0.1O3-δ（BCFN） mixed conductor to improve its oxygen transport behavior. The results show that the SDC-coated BCFN membrane exhibits a remarkably higher oxygen permeation flux（JO2） than the uncoated BCFN in the partial oxidation of coke oven gas（COG）. The maximum JO2 value of the SDC-coated BCFN is 18.28 mL ·min^-1·cm^-2 under a COG/air flux of 177 mL ·min^-1/353 mL ·min^-1 at 875℃ when the thickness of the BCFN membrane is 1 mm; this JO2 value is 23% higher than that of the uncoated BCFN membrane. This enhancement is likely because of the higher oxygen ionic conductivity of SDC, which supplies oxygen vacancies and accelerates oxygen exchange on the membrane/coating layer/gas three-phase boundary.

Effect of AIBI as Free Radical Initiator on Abrasive-Free Polishing of Hard Disk Substrate

To optimize the existing slurry for abrasive-free polishing(AFP)of hard disk substrate,a water-soluble free radical initiator,2,2-azobis[2-(2-imidazolin-2-yl)propane]dihydrochloride(AIBI)is introduced to the H2O2-based slurry.The polishing results show that,the material removal rate(MRR)of hard disk substrate polished with H2O2-based slurry containing AIBI is obviously higher than that without AIBI.The acting mechanism of the improved MRR is investigated.Electron paramagnetic resonances tests show that,by comparison with H2O2 slurry,H2O2-AIBI slurry provides higher concentration of hydroxyl radicals.Auger electron spectrometer analyses further demonstrate that the oxidation ability of H2O2-AIBI slurry is much greater than H2O2 slurry.In addition,potentiodynamic polarization tests show that the corrosion dissolution rate of hard disk substrate in H2O2-AIBI slurry is increased.Therefore that stronger oxidation ability and a higher corrosion dissolution rate of H2O2-AIBI slurry lead to higher MRR can be concluded.

Chemical Treatment of Carbon Nanotubes as Electrodes in Electrochemical Double-Layer Capacitors

Multi-walled carbon nanombes with homogeneous diameters （40 - 60 nm）, produced by chemical vapor deposition of hydrocarbon gas, are purified by nitric acids. Infrared and Raman studies indicate that oxygen containing surface groups, which are predominately carboxylic, phenolic and lactonic groups, are introduced into purified carbon nanotubes. Then three kinds of block-form porous tablets of carbon nanotubes are fabricated as electrodes in electrochemical double-layer capacitors. Using mounded mixture comprising carbon nanotubes and binder powders provides these tablets. Comparison of the effect of different processing on the structural performance of the capacitors is specifically investigated. Using chemically treated electrodes, electrochemical double-layer capacitors with a specific capacitance of about 33 F/g are obtained with 38 wt % H2SO4 as the electrolyte.

Study on the influence of standoff distance on substrate damage under an abrasive water jet process by molecular dynamics simulation

The process of a cluster-containing water jet impinging on a monocrystalline silicon substrate was studied by molecular dynamics simulation. The results show that as the standoff distance increases, the jet will gradually diverge. As a result, the solidified water film between the cluster and the substrate becomes "thicker" and "looser". The "thicker" and "looser" water film will then consume more input energy to achieve complete solidification, resulting in the stress region and the high-pressure region of the silicon substrate under small standoff distances to be significantly larger than those under large standoff distances. Therefore, the degree of damage sustained by the substrate will first experience a small change and then decrease quickly as the standoff distance increases. In summary, the occurrence and maintenance of complete solidification of the confined water film between the cluster and the substrate plays a decisive role in the level of damage formation on the silicon substrate. These findings are helpful for exploring the mechanism of an abrasive water jet.

Synthesis and formation mechanism of nanocrystalline ZrB_(2)-Al_(2)O_(3)composite powders via an amorphous precursor

ZrB_(2)-Al_(2)O_(3)composite powders were synthesized at 1100℃using a novel ZrB_(2)precursor and Al powders as raw materials.The final ZrB_(2)-Al_(2)O_(3)composite powders consisted of submicron Al_(2)O_(3)and nanosize ZrB_(2)(50-100 nm)particles,which were homogeneously mixed in microscale.Combined with thermodynamic calculation and experiment results,the formation mechanism of ZrB_(2)-Al_(2)O_(3)composite powders was proposed as follows:ZrB_(2)precursor first decomposed into ZrO_(2)and amorphousB2O3.Aluminothermic reduction of ZrO_(2) and B_(2)O_(3) generated Zr and B atoms and the coproducts Al_(2)O_(3),and then,a series of reactions between Zr atoms,B atoms and Al took place to form ZrB_(2)and Al_(3)Zr.Then,ZrB_(2),Al_(2)O_(3)and Al were obtained through a liquid-solid reaction between Al_(3)Zr andB2O3,which is the limiting step in the conversion process.When the Al_(3)Zr was exhausted,the reaction between Al,ZrO_(2)and B became the main reaction to obtain ZrB_(2)and Al_(2)O_(3).