应用在线电解修整磨削和磁流变光整加工组合工艺进行碳化硅的纳米加工

利用在线电解修整镜面磨削和磁流变光整加工技术对化学气相沉积碳化硅反射镜进行纳米级精度的加工。首先进行在线电解修整磨削，使反射镜面高效率加工成形，并获得较好的形状精度和表面质量；然后利用磁流变技术进行光整加工，以减少反射镜的亚表面损伤，提高表面质量，并通过修正加工，显著提高了工件表面的形状精度。对化学气相沉积碳化硅进行了一系列的加工试验，高效率地得到Rq=2．4nm（均方根偏差）的表面粗糙度和21．2nm的形状精度，并且对在线电解修整镜面磨削与磁流变光整加工所生成的表面特性进行了分析比较。     

Enhanced mechanical and thermal properties of nanodiamond reinforced low density polyethylene nanocomposites

In this study, the reinforcement effects of low-content hydrophilic nanodiamond (ND) on linear low-density polyethylene (PE) nanocomposites were investigated. ND was incorporated in PE via simple solution blending. The obtained PE/ND nanocomposites were characterized using scanning electron microscopy, ultraviolet–visible spectra, X-ray diffraction, tensile test, thermogravimetry, and differential scanning calorimetry. Generally, PE/ND nanocomposites with poor interfacial interaction cause large agglomerates, resulting in brittle and poor mechanical properties. Owing to the different natures of non-polar PE and polar ND, the higher the ND content, the larger the agglomerates formed in the nanocomposites. However, PE/ND nanocomposites show unique mechanical properties, that is, the Young's modulus, tensile strength, elongation at break, and toughness increased upon the incorporation of ND. The Young's modulus of the PE/ND nanocomposites exceeded the theoretical value calculated using the Halpin–Tsai model. In addition, the toughness increased by 18% at only 0.5 wt% ND loading. Furthermore, there was an increase in the thermal degradation temperature, melting temperature, and crystallization temperature.     

Dependence of alcohol vapor‐induced crystallization on gas and vapor permeabilities of poly(lactic acid) films

The effects of methanol and ethanol vapor‐induced crystallization on vapor and gas permeabilities and on the structure of poly(lactic acid) (PLA) films were systematically investigated. At high temperature conditions, the vapor permeability of PLA films decreased with increasing exposure time. The PLA films that were exposed to alcohol vapor became slightly cloudy, and no changes in chemical structure were observed. Alcohol vapor‐induced crystallization formed α‐crystal structure. The vapor permeability decreased with increasing crystallinity. However, nitrogen permeability slightly increased after vapor‐induced crystallization. The dependence of crystallinity on vapor and gas permeabilities was different from each penetrant. Total crystalline structures, including continuous crystal structures, remaining amorphous regions, and their interface depend on vapor and gas permeabilities. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40140.     

Synthesis and physical properties of poly(l‐lactic acid)‐poly(dimethyl siloxane) multiblock copolymers prepared by direct polycondensation

Multiblock copolymers consisting of poly(l ‐lactic acid) and poly(dimethyl siloxane) were prepared by the polycondensation of oligo(l ‐lactic acid) (OLLA) with dihydroxyl‐terminated oligo(dimethyl siloxane) and dicarboxyl‐terminated oligo(dimethyl siloxane). Copolymers with number‐average molecular weights of 18,000?33,000 Da and various content ratios of oligo(dimethyl siloxane) (ODMS) unit were obtained by changing the feed ratio of these oligomers. A film prepared from the copolymer with an ODMS content ratio of 0.37 exhibited two independent peaks at ?107°C and 37°C in the mechanical loss tangent for temperature dependence, suggesting the formation of microphase separation between the OLLA and ODMS segments. The film had a tensile strength of 3.2 MPa and a high elongation of 132%. The film also exhibited a high strain recovery even after repeated straining. The incorporation of dimethyl siloxane units as multiblock segments was confirmed to improve the flexibility of poly(l ‐lactic acid). © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40211.     

A model of carbon ion interactions in water using the classical trajectory Monte Carlo method

In this paper, model calculations for interactions of C(6+) of energies from 1 keV u(-1) to 1 MeV u(-1) in water are presented. The calculations were carried out using the classical trajectory Monte Carlo method, taking into account the dynamic screening of the target core. The total cross sections (TCS) for electron capture and ionisation, and the singly and doubly differential cross sections (SDCS and DDCS) for ionisation were calculated for the five potential energy levels of the water molecule. The peaks in the DDCS for the electron capture to continuum and for the binary-encounter collision were obtained for 500-keV u(-1) carbon ions. The calculated SDCS agree reasonably well with the z(2) scaled proton data for 500 keV u(-1) and 1 MeV u(-1) projectiles, but a large deviation of up to 8-folds was observed for 100-keV u(-1) projectiles. The TCS for ionisation are in agreement with the values calculated from the first born approximation (FBA) at the highest energy region investigated, but become smaller than the values from the FBA at the lower-energy region.     

Photoelectrochemical and photocatalytic properties of biphasic organic p- and n-type semiconductor nanoparticles fabricated by a reprecipitation process

The visible-light-responsive photoelectrochemical and photocatalytic properties of nanoparticles of C(60), partially hydrolyzed aluminum phthalocyanine chloride (denoted as AlPc), and a composite of the two are reported. The three types of nanoparticles were obtained through a reprecipitation method from N-methyl-2-pyrrolidone solutions of C(60), aluminum phthalocyanine chloride (AlPcCl), and their mixture, respectively. The nanoparticle composite's ultraviolet-visible absorption, diffuse-reflectance and Fourier transform IR spectra, X-ray diffraction pattern, and scanning electron microscopy image are all similar to the sum of those of the C(60) and AlPc particles, respectively. The nano-ordered composite exhibits p/n junctionlike photoelectrochemical characteristics, which were investigated in comparison with those of vapor-deposited C(60) (n-type), AlPcCl (p-type), C(60)/AlPcCl (n/p), and AlPcCl/C(60) (p/n) electrodes. The nanoparticle composite further shows photocatalytic activity for the decomposition of trimethylamine to carbon dioxide in a suspension system.     

Effect of X-ray exposure on the pharmaceutical quality of drug tablets using X-ray inspection equipment

Context: X-ray inspection equipment is widely used to detect missing materials and defective goods in opaque containers. Its application has been expanded to the pharmaceutical industry to detect the presence of drug tablets in aluminum foil press-through packaging. However, the effect of X-rays on the pharmaceutical quality of drug tablets is not well known.

Objective: In this study, the effect of X-rays on the pharmaceutical quality of drug tablets was investigated.

Methods: Exposure of acetaminophen, loxoprofen and mefenamic acid tablets to X-ray doses of 0.34?mGy (thrice the dose by X-ray scanning) to 300?Gy (maximum dose from our X-ray equipment) was demonstrated, and the samples were evaluated by formulation tests.

Results: Exposure to X-rays did not affect the pharmaceutical quality of the drug content. The samples exposed to X-rays exhibited almost the same profile in formulation tests (dissolution test, disintegrating test and hardness test) as control samples (0?Gy). The combination of X-ray exposure with accelerated temperature and humidity tests (six months) also did not affect the pharmaceutical quality. The color change of light-sensitive drugs (nifedipine and furosemide tablets) after X-ray exposure was negligible (Conclusion: The X-ray scanning and X-ray exposure under our experimental conditions did not affect the pharmaceutical quality of drug tablets.     

Catalyzed thermal decompositon of H2SO4 and production of HBr by the reaction of SO2 with Br2 and H2O

Decomposition of H₂SO₄ and production of HBr have been studied as a part of the research and development of the thermochemical hydrogen production from water. The catalytic activities of various metals and metal oxides on a porous alumina support were studied for the thermal decomposition of sulfuric acid in a fixed bed reactor. A Pt-Al₂O₃ catalyst gave a conversion of SO₃ close to the equilibrium at temperatures from 1073 to 1173 K and at a space velocity below 10 000 h^?1. It was also found that metal oxide catalysts such as CuO and Fe₂O₃ were as active as the Pt catalyst. To prepare SO₂-free HBr gas by the reaction between SO₂, Br₂ and H₂O, vapor-liquid equilibrium determinations for SO₂/Br₂/HBr/H₂SO₄/H₂O system were carried out at 298 K under atmospheric pressure. The unconverted SO₂ can be effectively removed by contacting the effluent gases with a HBr saturated aqueous solution containing an excess of Br₂.     

Influence of ambient temperatures on performance of a CO2 heat pump water heating system

In residential applications, an air-to-water CO₂ heat pump is used in combination with a domestic hot water storage tank, and the performance of this system is affected significantly not only by instantaneous ambient air and city water temperatures but also by hourly changes of domestic hot water consumption and temperature distribution in the storage tank. In this paper, the performance of a CO₂ heat pump water heating system is analyzed by numerical simulation. A simulation model is created based on thermodynamic equations, and the values of model parameters are estimated based on measured data for existing devices. The calculated performance is compared with the measured one, and the simulation model is validated. The system performance is clarified in consideration of seasonal changes of ambient air and city water temperatures.