块魂 拉伸

NBGI的《块魂 拉伸》将于今年12月17日登陆PSV。游戏以简单的操作和欢乐的游戏内容而为大家熟知。在本作中．系列的优点都得以保留。PSV版《块魂》的滚动方法将不同于以往,采用直接触摸的方式。直接触摸屏幕就能调整滚动的位置,更加直感的操作使得游戏操作更加简洁。也更富乐趣。     

Radiation Stability of Low-Viscosity Base Oils for Aerospace Engineering Control Systems

The results of radiation exposure on low–viscosity mineral bases for hydraulic oils for aerospace engineering control systems are reported. Isoparaffinic structures with different degrees of branching are best among the dearomatized low–viscosity oils with respect to radiation stability. Hydrogen and hydrocarbon gases are the basic components of the products of radiation decomposition of mixtures with a viscosity of 4 mm²/sec at 50°C.     

液晶共面取向的等离子处理方法

在受等离子辐照过的一些有机和无机的基板上，获得了高质量的液晶共面取向。与已知的用来改善顶部锚定及预倾角各向同性的等离子处理方法不同，新方法是将等离子束调整到倾斜射向待取向的基板。在所用的辐射参数范围内，所有基板上的LC取向的易取向轴(easy axis)都平行于等离子体传播方向。研究了LC的预倾角和锚定能与等离子束的入射角、辐照时间、能量以及辐照电流密度等的依赖关系。经等离子处理过的基板上，方位角、锚定能与用光取向方法得到的相近，而预倾角与摩擦产生的类似。透过率-电压曲线与等离子处理的和摩擦工艺处理的非常接近。与摩擦取向相同，等离子诱导的取向具有很高的温度和光照的稳定性。也考虑了采用等离子／偏振紫外光和等离子／摩擦处理等组合方法来制作LC图形。     

High Strength Stainless Austenitic CrMnCN Steels – Part I: Alloy Design and Properties

Generally the strength of stainless austenitic steels does not live up to their good corrosion resistance. Solid solution hardening by interstitial elements is a means of raising the strength, but is used only moderately because of poor weldability, which, however, is not required in various applications. The solubility of nitrogen is high in stainless austenite of steels with 18 mass% of Cr and Mn each, but low in the melt. Carbon reveals the opposite behaviour. Instead of producing high nitrogen steels by pressure metallurgy, about 1 mass% of C+N is dissolved in the melt at ambient pressure. The new cost‐effective C+N steel reaches a yield strength of 600 MPa, a true fracture strength above 2500 MPa and an elongation above 70 %. Conduction electron spin resonance revealed a high concentration of free electrons. Thus, the ductile metallic character of the C+N steel is enhanced, explaining the high product of strength times toughness. The high interstitial content requires rapid quenching to avoid an embrittling precipitation and respective intercrystalline corrosion.     

Tyl6, a novel Ty3/gypsy-like retrotransposon in the genome of the dimorphic fungus Yarrowia lipolytica

The novel LTR retrotransposon Tyl6 was detected in the genome of the dimorphic fungus Yarrowia lipolytica. Sequence analysis revealed that this element is related to the well-known Ty3 element of Saccharomyces cerevisiae and, especially, to the recently described Tse3 retrotransposon of Saccharomyces exiguus and to the del1-like plant retrotransposons. Tyl6 is 5108 bp long, is flanked by two identical long terminal repeats (LTR), each of 276 bp, and its ORFs are separated by a -1 frameshift. Both ORFs are intact and deduced translation products display a significant similarity with those of previously described Ty3/gypsy retrotransposons. Distribution of Tyl6 among Y. lipolytica strains of different origins was also analysed. A single copy of the novel retrotransposon is present in some commonly used laboratory strains, which are derivatives of the wild-type isolate YB423-12, whereas other strains of independent origin are devoid of Ty16. No solo LTR of Tyl6 was detected in the analysed strains.     

LanGT2 Catalyzes the First Glycosylation Step during landomycin A biosynthesis

The glycosyltransferase LanGT2 is involved in the biosynthesis of the hexasaccharide side chain of the angucyclic antibiotic landomycin A. Its function was elucidated by targeted gene inactivation of lanGT2. The main metabolite of the obtained mutant was identified as tetrangulol (4), the progenitor of the landomycin aglycon (7). The lack of the sugar side chain indicates that LanGT2 catalyzes the priming glycosyl transfer in the hexasaccharide biosynthesis: the attachment of a D-olivose to O-8 of the polyketide backbone. Heterologous expression of urdGT2 from S. fradiae Tü2717 in this mutant resulted in the production of a novel C-glycosylated angucycline (6).     

The design and realization of CoViD: a system for collaborative virtual 3D design

Many important decisions in the design process are made during fairly early on, after designers have presented initial concepts. In many domains, these concepts are already realized as 3D digital models. Then, in a meeting, the stakeholders for the project get together and evaluate these potential solutions. Frequently, the participants in this meeting want to interactively modify the proposed 3D designs to explore the design space better. Today’s systems and tools do not support this, as computer systems typically support only a single user and computer-aided design tools require significant training. This paper presents the design of a new system to facilitate a collaborative 3D design process. First, we discuss a set of guidelines which have been introduced by others and that are relevant to collaborative 3D design systems. Then, we introduce the new system, which consists of two main parts. The first part is an easy-to-use conceptual 3D design tool that can be used productively even by naive users. The tool provides novel interaction techniques that support important properties of conceptual design. The user interface is non-obtrusive, easy-to-learn, and supports rapid creation and modification of 3D models. The second part is a novel infrastructure for collaborative work, which offers an interactive table and several large interactive displays in a semi-immersive setup. It is designed to support multiple users working together. This infrastructure also includes novel pointing devices that work both as a stylus and a remote pointing device. The combination of the (modified) design tool with the collaborative infrastructure forms a new platform for collaborative virtual 3D design. Then, we present an evaluation of the system against the guidelines for collaborative 3D design. Finally, we present results of a preliminary user study, which asked naive users to collaborate in a 3D design task on the new system.     

Synthesis and flash sintering of zirconium nitride powder

Zirconium nitride (ZrN) is a transition metal nitride of great interest due to its excellent physical and chemical properties. This study aims to synthesize ZrN fine powders by a facile and low-cost urea route that avoids the use of any solvent. ZrCl₄ and urea mixtures were heat-treated at up to 1600˚C in nitrogen gas. The products were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and thermogravimetric analysis. The effects of different processing parameters such as metal to urea molar ratio, heat treatment temperature, and dwelling time on the product phase and stoichiometry were studied to understand the synthesis method. In addition, synthesized ZrN powder was consolidated into near fully dense single-phase bulk ceramic with a homemade flash sintering setup. A constant DC electrical field of ∼80 V/cm and pressure of ∼14 MPa at room temperature triggered flash sintering without pre-heating, and the entire process finished in 200 s. The composition, microstructure, density, hardness, and oxidation properties of the sintered pellet were also characterized.     

Stability of poly-α-olefin oils and methods for increasing it

The stability of poly-α-olefin oils with molecular mass of from 500 to 1000 is investigated. It is found that the molecular mass, temperature, and introduction of various antioxidizers affect the thermo-oxidative stability of oils. It is shown that poly-α-olefin oils with antioxidizers can be used as liquid dielectrics.     

Doping Rules and Doping Prototypes in A2BO4 Spinel Oxides

A₂BO₄ spinels constitute one of the largest groups of oxides, with potential applications in many areas of technology, including (transparent) conducting layers in solar cells. However, the electrical properties of most spinel oxides remain unknown and poorly controlled. Indeed, a significant bottleneck hindering widespread use of spinels as advanced electronic materials is the lack of understanding of the key defects rendering them as p‐type or n‐type conductors. By applying first‐principles defect calculations to a large number of spinel oxides the major trends controlling their dopability are uncovered. Anti‐site defects are the main source of electrical conductivity in these compounds. The trends in anti‐sites transition levels are systemized, revealing fundamental “doping rules”, so as to guide practical doping of these oxides. Four distinct doping types (DTs) emerge from a high‐throughput screening of a large number of spinel oxides: i) donor above acceptor, both are in the gap, i.e., both are electrically active and compensated (DT‐1), ii) acceptor above donor, and only acceptor is in the gap, i.e., only acceptor is electrically active (DT‐2), iii) acceptor above donor, and only donor is in the gap, i.e., only donor is electrically active (DT3), and iv) acceptor above donor in the gap, i.e., both donor and acceptor are electrically active, but not compensated (DT‐4). Donors and acceptors in DT‐1 materials compensate each other to a varying degree, and external doping is limited due to Fermi level pinning. Acceptors in DT‐2 and donors in DT‐3 are uncompensated and may ionize and create holes or electrons, and external doping can further enhance their concentration. Donor and acceptor in DT‐4 materials do not compensate each other, and when the net concentration of carriers is small due to deep levels, it can be enhanced by external doping.