Performance evaluation of snapshot isolation in distributed database system under failure-prone environment

Database systems are widely used in many fields. As the scale of database systems increases, more firms decide to deploy the database system in a distributed environment for the sake of data integrity fault tolerance. For guaranteeing the consistency of data, database management systems adopt isolation policies. This paper discusses probabilistic models for snapshot isolation of database management system. Snapshot isolation is an effective method to enhance the consistency of database system, although it degrades the system performance where the system has large network latency such as distributed database system. Also, under the failure-prone environment, a restart scheme is considered as one countermeasure. This paper proposes probabilistic models for the dynamics of snapshot isolation of database system and exhibits the optimization of system performance with respect to updating interval of snapshot isolation within the failure-prone environment from the analytical point of view. Numerical experiments are conducted to validate the effectiveness of analytical results by using real traffic data.     

Synthesis of novel photo-cross-linkable polymers with redissolution property

p-Styrenesulfonate derivatives having cycloaliphatic epoxide in a molecule, were synthesized. Oligomerization of the monomers and co-polymerization of the novel monomers with tert-butyl methacrylate were carried out. When the polymer films containing a photoacid generator (PAG) were irradiated, they became insoluble in solvents. The insoluble films became soluble in water on baking at 120-200 °C. The insolubilization and redissolution profiles were strongly affected by the structure of the monomer, irradiation and baking conditions, and a type of PAG used. The reaction mechanism was studied by TGA analysis and FT-IR spectroscopy.     

A novel thermosensitive polymer, poly(methyl 2-propionamidoacrylate), with geminal substituents

A novel thermosensitive polymer, poly(methyl 2-propionamidoacrylate) (PMPA), was prepared and the phase transition behavior in an aqueous solution was studied. PMPA have geminal substituents of propionamide and methoxy carbonyl in each monomer unit. It was found that PMPA shows the lower critical solution temperature (LCST) at 50.6 °C sharply. The LCST of PMPA was almost independent of the polymer concentration above 40 g/l, while, below 40 g/l, it decreased with the increasing polymer concentration. The effect of salt addition (NaCl, NaBr, and Na₂SO₄) on the LCST was also studied. The LCST of PMPA linearly decreased with the increasing concentration of each salt. The salting-out effect of these salts was in line with the Hofmeister series: Na₂SO₄>NaCl>NaBr.     

Catalytic hydrogenation of linoleic acid over platinum-group metals supported on alumina

Catalytic activity and selectivity for hydrogenation of linoleic acid (cis-9,cis-12 18:2) were studied on Pt, Pd, Ru, and Ir supported on Al₂O₃. Stearic acid (18:0) and 10 different octadecenoic isomers (18:1) in the products could be separated completely by using a new capillary column coated by isocyanopropyl trisilphenylene siloxane for gas-liquid chromatography. The monoenoic acid isomers and dienoic acid isomers in the products on the various catalysts showed different distributions. The catalysts exhibited nearly equal selectivity for stearic acid formation. The 12-position double bond in linoleic acid has higher reactivity than the 9-position double bond in catalytic hydrogenation on platinum-group metal catalysts. In addition to hydrogenation products of linoleic acid, geometrical and positional dienoic acid isomers (trans-9,trans-12; trans-8,cis-12; cis-9,trans-13; trans-9,cis-13; cis-9,trans-12 18:2), due to isomerization of linoleic acid during hydrogenation, were contained in the reaction products. Ru/Al₂O₃ exhibited the highest activity for isomerization of linoleic acid with the noble metal catalysts. Conjugated octadecadienoic acid isomers have been observed in products of the reaction on Pt/Al₂O₃, Ru/Al₂O₃, and Ir/Al₂O₃. Catalytic activities of noble metals for positional and geometric isomerization of linoleic acid during hydrogenation decreased in the sequence of Ru ≥ Pt > Ir » Pd.     

Mechanical Properties of Hot Isostatically Pressed Zirconia-Toughened Alumina Ceramics Prepared from Coprecipitated Powders

Amorphous Al₂O₃–ZrO₂ composite powders with 5–30 mol% ZrO₂ have been prepared by adding aqueous ammonia to the mixed solution of aqueous aluminum sulfate and zirconium alkoxide containing 2-propanol. Simultaneous crystallization of γ-Al₂O₃ and t -ZrO₂ occurs at 870°–980°C. The γ-Al₂O₃ transforms to α-Al₂O₃ at 1160°–1220°C. Hot isostatic pressing has been performed for 1 h at 1400°C under 196 MPa using α-Al₂O₃– t -ZrO₂ composite powders. Dense ZrO₂-toughened Al₂O₃ (ZTA) ceramics with homogeneous-dispersed ZrO₂ particles show excellent mechanical properties. The toughening mechanism is discussed. The microstructures and t / m ratios of ZTA are examined, with emphasis on the relation between strength and fracture toughness.     

Iodine-initiated,solid-state copolymerization of tetraoxane with 1,3-dioxolane in the presence of methylal. I. Fundamental study on beaker-scale copolymerization

The iodine-initiated, solid-state copolymerization of tetraoxane with 1,3-dioxolane in the presence of methylal has been studied on a beaker scale. It was found that tetraoxane can be easily copolymerized with 1,3-dioxolane by a small amount of iodine as initiator and gives oxymethylene copolymer with excellent thermal stability in a high yield. The copolymerization was largely influenced by the concentrations of iodine, 1,3-dioxolane, and methylal, i.e., the polymerization rate increased with increase not only in iodine but also in 1,3-dioxolane, and the thermal stability and the molecular weight of the copolymer were mainly affected by 1,3-dioxolane and methylal concentration, respectively.     

Novel super fast response vertical alignment‐liquid crystal display with extremely wide temperature range

We have developed a novel super fast response (SFR) thin‐film transistor liquid crystal display (TFT‐LCD) with an extremely wide temperature range. Nematic liquid crystal molecules with positive dielectric anisotropy are vertically aligned initially. Any gray‐to‐gray response is forcibly controlled by applying an electric field. Response times of the SFR TFT‐LCD are over several times shorter than those of conventional LCDs such as vertical alignment or in‐plane switching LCDs.     

Application of accelerators for the research and development of scintillators

We introduce experimental systems which use accelerators to evaluate scintillation properties such as scintillation intensity, wavelength, and lifetime. A single crystal of good optical quality is often unavailable during early stages in the research and development (R&D) of new scintillator materials. Because of their beams' high excitation power and/or low penetration depth, accelerators facilitate estimation of the properties of early samples which may only be available as powders, thin films, and very small crystals. We constructed a scintillation spectrum measurement system that uses a Van de Graaff accelerator and an optical multichannel analyzer to estimate the relative scintillation intensity. In addition, we constructed a scintillation time profile measurement system that uses an electron linear accelerator and a femtosecond streak camera or a microchannel plate photomultiplier tube followed by a digital oscilloscope to determine the scintillation lifetimes. The time resolution is approximately 10 ps. The scintillation spectra or time profiles can be obtained in a significantly shorter acquisition time in comparison with that required by conventional measuring systems. The advantages of the systems described in this study can significantly promote the R&D of novel scintillator materials.     

Tribological properties of asperity arrays coated with self-assembled monolayers

The effects of a self-assembled monolayer (SAM) coating on the friction and pull-off forces were determined by using two-dimensional asperity arrays on silicon wafers. The arrays were coated with SAM composed of one of five different alkylchlorsilanes. First, two-dimensional asperity arrays were created by using a focussed ion beam (FIB) system to mill patterns on silicon plates. Each silicon plate had different patterns of equally spaced asperities. Each pattern (5 × 5 μm²) had a different radius of curvature of the asperity peaks, ranging from about 200 to 2500 nm. Then, each silicon plate was immersed in a solution of a different alkylchlorsilane in hexane (either hexyltrichlorosilane, octyltrichlorosilane, dodecyltrichlorosilane, tetradecyltrichlorosilane, or octadecyltrichlorosilane), thus coating the asperity arrays with SAM. The friction and pull-off forces on the SAM-coated arrays were measured by using an atomic force microscope (AFM) that had a square flat probe. The pull-off force for SAM-coated silicon was roughly proportional to the radius of curvature of the asperity peaks. The magnitude of the pull-off force corresponded approximately to the capillary force calculated by using the contact angle of water on the surface of SAM. The friction coefficient correlated with the inverse of the alkyl-chain length of the SAM.     

Laser ion source with solenoid for Brookhaven National Laboratory-electron beam ion source

The electron beam ion source (EBIS) preinjector at Brookhaven National Laboratory (BNL) is a new heavy ion-preinjector for relativistic heavy ion collider (RHIC) and NASA Space Radiation Laboratory (NSRL). Laser ion source (LIS) is a primary ion source provider for the BNL-EBIS. LIS with solenoid at the plasma drift section can realize the low peak current (～100 μA) with high charge (～10 nC) which is the BNL-EBIS requirement. The gap between two solenoids does not cause serious plasma current decay, which helps us to make up the BNL-EBIS beamline.