Automatic extraction of citation information in Japanese patent applications

The need for academic researchers to retrieve patents and research papers is increasing, because applying for patents is now considered an important research activity. However, retrieving patents using keywords is a laborious task for researchers, because the terms used in patents for the purpose of enlarging the scope of the claims are generally more abstract than those used in research papers. Therefore, we have constructed a framework that facilitates patent retrieval for researchers, and have integrated research papers and patents by analysing the citation relationships between them. We obtained cited research papers in patents using two steps: (1) detection of sentences containing bibliographic information, and (2) extraction of bibliographic information from those sentences. To investigate the effectiveness of our method, we conducted two experiments. In the experiment involving Step 1, we prepared 42,073 sentences, among which a human subject manually identified 1,476 sentences containing citations of papers. For Step 2, we prepared 3,000 sentences, in which the titles, authors, and other bibliographic information were manually identified. We obtained a precision of 91.6%, and a recall of 86.9% in Step 1, and a precision of 86.2% and a recall of 85.1% in Step 2. Finally, we constructed an information retrieval system that provided two methods of retrieving research papers and patents. One method was retrieval by query, and another was from the citation relationships between research papers and patents.     

An extreame disposition method for low-level radioactive wastes using supercritical water (3)

Disposition of low-level radioactive wastes has been performed in supercritical water with RuO₂ as a catalyst without the addition of any oxidizing materials. These wastes arose from nuclear power plants etc., constituting of nonflammable organic materials, such as fire resistant sheeting and rubber gloves. We investigated the distribution behavior of iron and cobalt attached to nonflammable organic materials, in solid, liquid and gas phases during the decomposition of this method. The distributions of these elements under various conditions (initial amounts) were determined by using their radioisotopes as simulated low-level radioactive wastes in order to ease the detection of trace amounts of elements even in solid and gas phases. Iron and cobalt were found only in the solid phase when non-radioactive iron hydroxide was added as a precipitation reagent before the supercritical-water reaction.     

An X-ray absorption approach to mixed and metallicity-sorted single-walled carbon nanotubes

Carbon based structures have been widely studied by X-ray absorption (XAS), also called NEXAFS, which is a very useful bulk probing method that allows examining the unoccupied density of states (DOS) and the site selective bonding environment. Two very well known spectral features in the XAS core level spectrum are the σ* and π* bands, and both have been analyzed in several studies for graphitic-like systems. However, among all the carbon materials, the unique one-dimensional electronic properties attributed to single-walled carbon nanotubes (SWCNTs) exhibit features that reveal clearly their electronic structure in the core level XAS spectrum. In this article, we outline the C1s response in XAS, which is related to the DOS of the conduction band in SWCNTs and its fine structure, revealed by experiments performed on metallicity-sorted SWCNT material. The progress in the identification of changes in the site selective conduction band electronic structure with XAS is discussed in detail.     

FI Catalysts: A Molecular Zeolite for Olefin Polymerization

A bis(phenoxyimine) group 4 transition metal catalyst (now known as FI catalysts) can discern ethylene from a mixture of ethylene and propylene at more than 99% selectivity. Denisty function theory (DFT) calculations revealed a spatially confined reaction site in the transition states of the migratory insertion which is just the right size for an ethylene molecule but too small for a propylene one. The substituents adjacent to the phenoxy‐oxygens are of crucial importance in developing the size/shape‐selectivity.     

Vortex–Antivortex-Pair Lattices in Spin–Orbit Coupled Bose–Einstein Condensates

We investigate theoretically the ground states of Bose–Einstein condensates with Rashba spin–orbit coupling in optical lattices within mean-field framework. We obtain numerically the Bloch states and energy spectrum for the single particle Hamiltonian, meanwhile the analytical solution of Bloch states is also presented. For a spin–orbit coupling Bose–Einstein condensates with a weak interaction, we show the existence of the vortex–antivortex-pair lattices state by simulating the Gross–Pitaevskii equation.     

Effect of annealing on d.c. conductivity of V2O5-SnO-TeO2 glasses

The d.c. conductivity (σ) of V₂O₅-SnO-TeO₂ glasses prepared by the press-quenching method was studied at temperatures from room temperature (RT) to 473 K, and the effect of annealing on σ was investigated. The conductivity of 50V₂O₅·20SnO·30TeO₂ glass was determined to be 3.98×10⁻⁴ Scm⁻¹ at 473 K and was unchanged for annealing (6–48 h) at 493 K, lower than T_g = 501 K, while its density increased with annealing time. These glasses were found to be n-type semiconductors, and the conduction was confirmed to be due to adiabatic small polaron hopping for V₂O₅ ≧ 50 mol%, and non-adiabatic for V₂O₅ < 50 mol%. The activation energy for conduction, W, decreased with annealing time. Variations in oxygen molar volume of the glasses with annealing time inferred a change in glass structure, from loosely to closely packed, resulting in a decrease in vanadium ion spacing with annealing. This caused an increase in the polaron band width, producing a decrease in polaron hopping energy and W. The effect of annealing time on the density of 50V₂O₅·20SnO·30TeO₂ glass was explained adequately by Winter's formula.     

Catalytic Behavior of Bis(Pyrrolide-Imine) and Bis(Phenoxy-Imine) Titanium Complexes for the Copolymerization of Ethylene with Propylene, 1-Hexene,or Norbornene

This contribution reports the catalytic behavior of bis(pyrrolide-imine)Ti complexes 1 and 2 , [2-(RNCH)-C₄H₃N]₂TiCl₂ ( 1 , R = Ph; 2 , R = cyclohexyl), and bis(phenoxy-imine)Ti complex 3 , [2-(Ph-NCH)-3-t Bu-C₆H₃O]₂TiCl₂ for the copolymerization of ethylene with propylene, 1-hexene, or norbornene. An inspection of the X-ray structures of complexes 1–3 suggested that complexes 1 and 2 with pyrrolide-imine ligands would provide more space for olefin polymerization than complex 3 with phenoxy-imine ligands. In addition, DFT calculations also showed that active species derived from complexes 1 and 2 possess higher electrophilicity of the Ti center compared to that from complex 3 . Complexes 1 and 2 on activation with methylalumoxane (MAO) had higher affinity for propylene and 1-hexene and incorporated higher amounts of propylene ( 1 ; 30.5 mol%, 2 ; 23.4 mol%) and 1-hexene ( 1 ; 1.9 mol%, 2 ; 1.7 mol%) than complex 3 (propylene; 4.5 mol%, 1-hexene; 0.4 mol%). The incorporation levels of propylene and 1-hexene displayed by complexes 1 and 2 were lower than those for Cp₂TiCl₂ (propylene; 41.6 mol%, 1-hexene; 5.1 mol%) under identical conditions. In contrast, complexes 1 and 2 exhibited higher incorporation ability for norbornene and produced copolymers with much higher norbornene contents ( 1 ; 32.0 mol%, 2 ; 26.5 mol%) than Cp₂TiCl₂ (1.2 mol%) under the same conditions. Additionally, complex 3 also promoted higher norbornene incorporation (4.3 mol%) than Cp₂TiCl₂ and provided a copolymer with extremely narrow molecular weight distribution (M_w/M_n 1.14). A correlation exists between electrophilicity of the Ti center in active species and norbornene incorporation.     

Continuous path control of a 5-DOF parallel-serial hybrid robot

Using the 5-degree of freedom parallel-serial hybrid robot, to realize the de-burring, new forward and inverse kinematic calculation methods based on the “off-line teaching” method are proposed. This hybrid robot consists of a parallel stage section and a serial stage section. Considering this point, each section is calculated individually. And the continuous path control algorithm of this hybrid robot is proposed. To verify the usefulness, a prototype robot is tested which is controlled based on the proposed methods. This verification includes a positioning test and a pose test. The positioning test evaluates the continuous path of the tool center point. The pose test evaluates the pose on the tool center point. As the result, it is confirmed that this hybrid robot moves correctly using the proposed methods.