Structural analysis of Ti-Fe thin films prepared by pulsed laser deposition

Titanium iron oxide (Ti-Fe-O) thin films have been successfully deposited by pulsed laser deposition (PLD). Experiments were carried out by using some targets. One was a Ti-50 at.% Fe-sintered target, while the others were Ti and Fe plates with various surface area ratio [S_R=S_Fe/(S_Fe+S_Ti)] from 30 to 70%. The thin films were analyzed by X-ray diffractometry, Rutherford backscattering spectroscopy (RBS) and transmission electron microscopy (TEM). From XRD analysis, the main phase in the thin films deposited at S_R=30 and 50% was β-Ti (Fe). By increasing S_R to 70%, the main phase of the thin film changed to TiFe. By phase diagram, composition of TiFe must be between Ti-47.5-50.3 at.% Fe at a temperature of 1085 °C. However, the composition of the thin film deposited at S_R=70% was found to be Ti_0.15Fe_0.62O_0.23. Thus, the composition of Fe in the thin film was much greater than the solubility limit. This fact suggests two possibilities. One is that the thin films, which we have deposited, were in a metastable state. The other is that metal oxides of amorphous state could be contained in the thin film.     

Polypropylene plasticization and photodegradation with a TiO2/poly(ethylene oxide)/methyl linoleate paint photocatalyst system

The photodegradation of polypropylene (PP) film was performed by a TiO₂/polyethylene oxide (PEO)/plant oil paint photocatalyst system. The photodegradation underwent two stages of development as follows: Initially PP reacted with linoleic acid radical originated from the photoreaction of plant oil component. Second, the linoleic acid graft‐polymer was decomposed, and then PP chain scission was caused. The process was studied using methyl linoleate (ML) in detail. The melting point of the 24 h‐photodegraded PP slightly decreased, and those of the 48 h‐ and 96 h‐ones drastically did as compared with the pristine PP. The crystallinity (χ_c) decreased at the 48 h photodegradation time and drastically increased at the 96 h one. The 24 h‐photodegraded PP showed the 77% Young's modulus, 88% tensile strength, and 103% strain at break values to those of the pristine PP. The ML graft‐polymerization and decomposition brought about the PP plasticizing and chemi‐crystallization, causing the PP degradation. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39909.     

Analog Circuit Design Methodology in a Low Power RISC Microprocessor

There are various kinds of analog CMOS circuits in microprocessors. IOs, clock distribution circuits including PLL, memories are the main analog circuits. The circuit techniques to achieve low power dissipation combined with high performance in newest prototype chip in the Super H RISC engines are described. A TLB delay can be decreased by using a CAM with a differential amplifier to generate the match signal. The accelerator circuit also helps to speed up the TLB circuit, enabling single-cycle operation. A fabricated 96-mm² test chip with the super H architecture using 0.35-m four metal CMOS technology is capable of 167-MHz operation at 300 Dhrystone MIPS with 2.0-W power dissipation.     

A comparative study on the thermally enhanced reorientation between random and diblock methacrylate copolymers with photo-cross-linkable mesogenic side groups by irradiating with linearly polarized ultraviolet light

The thermally enhanced photoinduced reorientation behavior of random and diblock copolymer films of methyl methacrylate and methacrylate with a photo-cross-linkable 4-(4-methoxycinnamoyloxy)biphenyl (MCB) side groups was investigated by irradiating with linearly polarized ultraviolet light and subsequently annealing. Random copolymers were synthesized by free radical copolymerization, while diblock ones were obtained by an atom transfer radical polymerization method with a PMMA macroinitiator. The photoinduced optical anisotropy was thermally amplified when the copolymer exhibited a liquid crystalline phase. The random copolymers with a high composition of MCB side groups reverted the orientation direction and inhibited molecular aggregation. For the diblock copolymers, the reorientation behavior was analogous to the methacrylate homopolymer with MCB side groups and transmission electron microscopy revealed a phase separation structure with molecular orientation of the MCB groups.     

跳跃式移动机构的移动机理及实验研究

介绍了一种新型跳跃式移动机构,阐述了该机构的移动机理及其控制方法.跳跃式移动机构采用小型振动电机作为驱动,利用电机内偏心轮的旋转所产生的周期性的向心力及与工作表面的间歇性摩擦力的共同作用,实现机构的跳跃移动,两个不同放置位置的电机的组合运用,可实现机构可调速的直线运动和回转运动,通过一系列实验.验证了跳跃式移动机构可实现二维平面内的自由移动.     

Preparation of Cr(N,O) thin films by RF reactive unbalanced magnetron sputtering

Chromium oxynitride thin films were deposited by radio-frequency (RF) reactive unbalanced magnetron sputtering at various O₂ flow rates onto Si(100) and glassy carbon substrates. The compositions of the thin films were analyzed by Rutherford backscattering spectroscopy. The thin films were found to contain up to 44 at.% oxygen. In Fourier-transform infrared spectra, a peak attributed to the Cr-N bond of CrN was observed, but no peak attributable to the Cr-O bond of Cr₂O₃ was found. The textures of the thin films were observed by transmission electron microscopy, which revealed that samples had a columnar structure. The hardness of the thin films was measured by nanoindentation. The hardness increased from 20 GPa to a maximum value of 31 GPa with increasing oxygen content.     

One-pot synthesis of hierarchically macro/mesoporous Al2O3 monoliths from a facile sol–gel process

Based on the preparation of ordered mesoporous Al₂O₃ powder using P123/isopropoxide aluminum/HNO₃ reaction system, hierarchically macro/mesoporous alumina monoliths were successfully fabricated by introducing PEG8000 as the phase-segregation initiator to generate macropores. The effects of PEG8000 and P123 contents on the monolithic and hierarchical morphology were investigated systematically. With appropriate selection of the starting composition, monolithic skeletons with bimodal macropores interconnected by mesostructured walls can be synthesized in both the dried gels and calcined samples. The well-defined macropores are in close-celled structure dispersed in large-sized mesoporous matrix. The mesopore size can be regulated by adjusting the PEG8000 content while its shape is governed by P123 content. The well-developed alumina monolith, MMA-P20, exhibits high surface area of 287 m²/g and narrowly distributed mesopores with median size of 13 nm after calcinaton.     

Plausible guard effect on the active sites of heterogeneous Ziegler–Natta catalyst by coordinating monomers and growing polymer chains in the initial stage of propene polymerization

Investigation of propene polymerization by a modified stopped‐flow technique using TiCl₄/ethylbenzoate(EB)/MgCl₂ Ziegler–Natta catalyst with or without pretreating the catalyst with triethylaluminium (TEA) within an ultra‐short period (ca 1 s) was conducted to gain new understanding of the nature of active sites related to TEA in the early stage of polymerization. When the catalyst was pretreated by a cocatalyst, deactivation behaviour was clearly observed, even within an extremely short pretreatment period. In contrast, without pretreatment, the deactivation of active sites can be neglected within the polymerization period indicating that the activated Ti species might be protected from deactivation by TEA when monomer is present in the system. A plausible guard effect on the active sites by coordinating monomer and growing polymer chains in the initial stage of polymerization is proposed to account for this phenomenon. Copyright © 2004 Society of Chemical Industry