Hydrothermal reactions of fumed silica with lime at 80°C were studied at starting Ca/Si of 0.8–2.0 and water/solid ratio of 20 by weight under periods of reaction time from 10 to 100 days.In the early ages of reaction, CSH having weak and diffuse basal reflections between 10–15Å was formed. On prolonging the reaction, CSH from the starting Ca/Si of 1.2–1.5 crystallised to jennite, and that from the starting Ca/Si of 0.9 to 14Å tobermorite.Lattice parameters were determined on the well crystalline jennite obtained by the reaction for 100 days at the starting Ca/Si of 1.4; i.e. ao 10.59, bo 7.21, co 10.82Å, α 99.60°, β 97.78°, γ 109.85°. Its crystals were lath-like elongated parallel to b with (001) cleavage.It was confirmed that the synthetic jennite was converted to meta-jennite by losing a part of its water on heating in air at 90°C. At higher temperatures it became poorly crystalline, and then crystallised to β-CaSiO3 and β-Ca2SiO4 at 800°C. 相似文献
A poled ferroelectric LiNbO3 single crystal with high spontaneous polarization was employed as a catalyst support, and the static and dynamic effects of the polar substrate surfaces on the adsorptive and catalytic properties of thin film catalysts deposited were shown. For the static effect, it was demonstrated that the surface conductivity of copper and metal-free phthalocyanine films increased by the adsorption of NO gas, to a larger extent, when the substrate was the negative polar surface, compared to the positive one. The role of the polar substrates is explained In terms of a band bending model. For the dynamic effect, the Rayleigh surface acoustic wave generated on the LiNbO3 substrate was shown to enhance the catalytic activity for ethanol oxidation on Cu and Ag thin film catalysts deposited on the propagation path. It is proposed that the catalyst activation is mainly due to an electric Held produced. The use of poled LiNbO3 is suggested to be effective for the development of a device-type catalyst with activity controllable functions. 相似文献
Curing catalyst for epoxy resins was newly found. The catalyst consists of aluminum complex and silanol. Lack of one component of the pair does not cure epoxy resins. The epoxy resins cured with the catalyst are characterized by excellent electrical properties, especially at high temperature, due to the absence of strong acid species in the cured epoxy resin matrix. Heat-resistant property of the resin was also excellent. These properties were compared with those of epoxy resin cured with commonly used BF3 complex. 相似文献
Control of microstructure in the Al2O3/LaAl11O18 system was performed. Elongated alumina grains were formed by doping with small addition of silica, and 20 vol% lanthana- luminate was formed in situ by the reaction of LaAlO3- A12O3 in an alumina matrix. Strengths of over 600 MPa and a high fracture toughness (6 MPa.m1/2) were achieved in the material with both elongated A12O3 grains and LaAl11O18 platelets. Generally antagonistic properties such as strength and fracture toughness have been made compatible in the same ceramic system. 相似文献
Novel Lu-α-SiAlON ceramics were produced by hot pressing mixtures of Si3N4, Lu2O3, AlN, and Al2O3 at 1950°C for 2 h in a nitrogen atmosphere. The resultant SiAlON was fully dense and possessed a uniform, equiaxed microstructure with a grain size of ∼1 μm, which resulted in a high hardness of >19 GPa. In addition to high hardness, the sample showed very high optical transparency in the visible light region, with >70% transmission at higher wavelengths. This high transparency was attributed to the uniform, dense microstructure and lack of residual grain-boundary phase. 相似文献
Summary: Polyacrylonitrile (PAN) particles with micro‐size ranges (0.15–2 μm) were prepared by emulsion and dispersion polymerizationa and in supercritical carbon dioxide media. The PAN particles were blended with Nylon 6 (PA6) at 220 °C by using a miniature mixer; it was found that melt‐mixing was possible for PAN‐rich compositions as high as 70 wt.‐%. Blends were characterized by scanning electron microscopy, IR, viscosity measurements, differential scanning calorimetry, and dynamic mechanical thermal analysis (DMTA). The size and shape of original PAN particles were retained in PAN/PA6 blends. The useful range to blend PAN particles size was less than 1 μm in terms of shape retention of the PAN particles in blends. Blends with 40 wt.‐% PAN content were found to be melt‐processable. The elastic modulus was higher for PAN/PA6 blends than pure PA6.
SEM photograph of PAN‐SC/PA6 blend with a 40/60 weight ratio. 相似文献
In the current work, we prepared a TiO2 coating on stainless mesh using electrophoretic deposition (EPD), and applied voltage to a stainless mesh to examine the synergy effect on photocatalysis of both 1,4-dioxane and ethylene glycol diformate (EGDF), a main intermediate of the photocatalysis of 1,4-dioxane. The photocatalytic decomposition rate of 1,4-dioxane depends on applying voltage under diffusion-limited reaction conditions. Ethylene glycol diformate and 1,4-dioxane exhibited inverse voltage dependence. Voltage swing provides high-efficiency photocatalysis of 1,4-dioxane while suppressing EGDF formation. This method will be effective for a photocatalysis system containing several chemicals, each with different voltage dependence. 相似文献
The catalytic activity of LaCoO3–-based mixed oxides for the oxidative coupling of methane has been tested by TPR and cyclic reaction. Characterization has been done by XRD, TGA and Mössbauer spectrometry. It is likely that the perovskite-crystal structure containing hypervalent metal ions has an important role and that unique structural oxygen species in the perovskite contribute to the partial oxidation of methane. 相似文献
The miscibility of poly(methyl methacrylate) (PMMA) and styrene-acrylonitrile random copolymers (SAN) blends was investigated on the basis of the Flory—Orwoll—Vrij equation of state theory. To obtain the equation of state parameters (P*, V*sp, T*: characteristic parameters), the pressure—volume—temperature (PVT) behaviour was measured for PMMA and a series of SANs with various acrylonitrile contents. The exchange energy parameter Xij was also calculated by fitting the theory to some phase diagrams of PMMA/SAN blends. The Flory—Huggins interaction parameter χ was separated into two contributions based on the equation of state theory for mixtures: the exchange energy term χinter and the free volume term χfree. Both the temperature and copolymer composition dependences of χinter and χfree were estimated by calculations using the equation of state parameters. There exists a region in which χinter is negative, leading to a miscibility window in PMMA/SAN blends. However, the immiscibility at high temperatures in the blends cannot be explained only by χinter; it is caused by the free volume contribution, χfree. The miscibility window behaviour in PMMA/SAN blends may be explained within the framework of the equation of state theory. 相似文献