序号 | 专利名 | 申请号 | 申请日 | 公开(公告)号 | 公开(公告)日 | 发明人 |
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141 | Fluorinated pitch and production of the same | JP23583386 | 1986-10-03 | JPS62275190A | 1987-11-30 | WATANABE NOBUATSU; HIGASHIHARA HIDEKAZU; MATSUMURA YUJI; FUJIMOTO HIROYUKI |
PURPOSE:To easily obtain fluorinated pitch having excellent lubricating ability, water- and oil-repellent properties, and chemical resistance and suitable as a battery active material and having film forming capability at a low cost in a high yield through vacuum vapor deposition, by directly reacting pitch with fluorine in a fluorine atmosphere. CONSTITUTION:Pitch, such as isotropic pitch, (hydrogenated)mesophase pitch, or mesocarbon microbeads, is directly reacted with fluorine in a fluorine atmosphere under a pressure of 0.07-1.5 atm at a temperature of 0-350 deg.C to attain a fluoride conversion of 100% or more. The fluorinated pitch thus obtd. has an F to C atomic ratio of 0.5-1.8 and exhibits the max. intensity peak around 2theta=13 deg. and a peak with a lower intensity than that of the max. peak around 2theta=40 deg. in a powder X-ray diffraction pattern. Further, it exhibits, in an X-ray photoelectron spectral analysis, a peak of CF group at 290.0+ or -1.0 eV and a peak of CF2 group around 292.5+ or -0.9 eV, with the intensity ratio of the CF2 group peak to the CF group peak being 0.15-1.5. The fluorinated pitch has a contact angle (30 deg.C) for 141+ or -8 deg. against water. | ||||||
142 | Toner | JP2012085208 | 2012-04-04 | JP2013214005A | 2013-10-17 | KABURAGI TAKESHI; YOSHIZAKI KAZUKI; ABE NOBUHISA; NAGASHIMA YUJIRO; MOCHIZUKI SHINSUKE |
PROBLEM TO BE SOLVED: To provide a toner having excellent storage stability or durable stability under a high temperature and high humidity environment and also having low-temperature fixability and hot off set resistance property.SOLUTION: A toner contains toner particles including: (1) a binder resin; (2) a coloring agent; (3) ester wax; (4) a monomer having a sulfonic acid group, a sulfonate group or a sulfonic acid ester group and a copolymer of a styrene monomer and an acrylic acid ester or a methacrylic acid ester. The binder resin is a styrene-acrylic resin. With regard to the sum of numbers of atoms of respective chemical elements of carbon atoms, oxygen atoms, nitrogen atoms and sulfur atoms obtained through a surface analysis of the toner particles by X-ray photoelectron spectroscopy (XPS), the sulfur atoms represent 0.05%-0.50% by number. When the toner particles are applied on an adhesive face of an adhesive tape, and the tape with the applied toner particles is pressed onto a glass and left under an environment of 30°C and 95% for 60 days, and thereafter removing the tape, a styrene-acrylic resin component amount remaining on the glass is set as (A), and an amount when left under an environment of 50°C and 95% for 2 days is set as (B), (A) and (B) satisfy: (A)≤0.30 mass%, and 0.25 mass%≤(B)≤0.60 mass%. | ||||||
143 | Battery electrode material, its manufacture, and electrochemical battery | JP19557298 | 1998-07-10 | JP2000030715A | 2000-01-28 | OGINO SEIJI; TOKUDA NOBUYUKI |
PROBLEM TO BE SOLVED: To enhance the efficiency of a battery, by introducing C-O bonds into surfaces of a fiber fabric made of carbon fiber or graphite fiber or carbon fiber/graphite fiber having a degree of oxidation shown by a specific ratio of the number of oxygen atoms to that of carbon atoms found by X-ray photo-electron spectroscopy, by means of plasma treatment, photochemical treatment, or ion implantation. SOLUTION: Preferably, the ratio of the number of oxygen atoms to the number of carbon atoms, showing a degree of oxidation of fiber, is 0.1 to 3.0, and the R value by Raman spectrometry analysis, showing a degree of graphitization, is 0.1 to 3.0, and especially, 0.1 to 1.2. By this, graphite fiber having large internal resistance can be used as an electrode material, the degree of oxidation of surfaces is raised more easily in a shorter time than by a heat-treatment method, and also reactive surface areas are increased by fine cracks generated. Preferably, when such treatment is performed on one side or both sides of a fiber fabric, oxygen is used, and when only one side is treated, fluorine is used. It is desirable that the concentration of C-O bonds is gradually decreased from the surface toward the interior, and that C-O bonds exist on one side while C-F bonds on the other side. COPYRIGHT: (C)2000,JPO | ||||||
144 | METHOD FOR PRODUCING A STEEL SHEET FOR A CONTAINER | EP11759393.9 | 2011-03-22 | EP2551377B1 | 2017-09-13 | TACHIKI, Akira; HIRANO, Shigeru; YOKOYA, Hirokazu; NODA, Masakazu; NISHIDA, Hiroshi; HASEGAWA, Kazushige |
145 | Non-Oriented Electrical Steel Sheet Having High Magnetic Flux Density And Motor | US14909978 | 2014-08-11 | US20160203896A1 | 2016-07-14 | Tadashi NAKANISHI; Shinji KOSEKI; Yoshihiko ODA; Hiroaki TODA |
A non-oriented electrical steel sheet having a chemical composition comprising C: not more than 0.010 mass %, Si: 1.0-7.0 mass %, Mn: 0.001-3.0 mass %, sol. Al: 0.0001-3.5 mass %, P: 0.01-0.2 mass %, S: not more than 0.010 mass %, N: not more than 0.010 mass % and the remainder being Fe and inevitable impurities, wherein a ratio (P120/Fe700) of a peak-peak height P120 of P near to an electronic energy of 120 eV to a peak-peak height Fe700 of Fe near to an electronic energy of 700 eV in an Auger differential spectrum obtained by analyzing a broken surface of a grain boundary through Auger electron spectroscopy is not less than 0.1 and a sheet thickness is 0.10-0.50 mm, and a motor using such a non-oriented electrical steel sheet as an iron core. | ||||||
146 | Full color image forming method | JP32089193 | 1993-11-29 | JPH07152217A | 1995-06-16 | YAMAZAKI MASUO; NISHIMURA KATSUHIKO; TANIGAWA KOICHI |
PURPOSE:To provide a full color image forming method by which toner is prevented from being welded and stuck to a photoreceptor and an intermediate transfer body and an image is efficiently transferred even to a small-sized transfer material. CONSTITUTION:A toner image is formed on a photoreceptor 1 where a compound having fluorine and/or silicon atoms measured by X-ray photoelectron spectroscopy for chemical analysis exists on the surface layer of the photoreceptor having a laminated structure consisting of a charge generating layer and a charge transporting layer on a conductive supporting body and the ratio of the atoms to a carbon atom shows F/C=0.03 to 1.00 and Si/C=0.03 to 1.00 with toner particles in which SF-1 measured by Luzex is 100 to 110 and 5 to 30wt.% low softening point substance is contained. The toner image on the photoreceptor is transferred on the intermediate transfer body 5, a transfer roller 7 is brought into contact with a transfer material 6, and the toner image on the intermediate transfer body is transferred to the transfer material, then the toner image on the transfer material is thermally fixed on the transfer material by a heating means. | ||||||
147 | Method of processing nucleic acids | US619048 | 1996-03-20 | US5796101A | 1998-08-18 | Richard Allan Haight; Paul Fredrich Seidler |
A laser based tunable high resolution ESCA (Electron Spectroscopy for Chemical Analysis) system in which harmonics of a subpicosecond laser source are used to carry out core level photoemission is provided wherein photon energies tunable to 80 eV have been achieved and energies up to 150 eV or more are possible. The harmonic light is of extremely narrow bandwidth and spectrally bright which can be focussed by using reflective optics of gratings to an extremely small spot of well below one micron to permit high spatial resolution. When used in conjunction with appropriate electron objects, high resolution chemically sensitive mapping of device-size features is possible. | ||||||
148 | Semiconductor material, production method thereof and semiconductor device | EP06255519.8 | 2006-10-26 | EP1783250A2 | 2007-05-09 | Seki, Akinori c/o Toyota Jidosha KK; Tani, Yukari c/o Japan Fine Ceramics Center; Shibata, Noriyoshi c/o Japan Fine Ceramics Center |
A semiconductor material having a stepwise surface structure of (0001)-plane terraces and (11-2n)-plane steps [n≥0] on the SiC substrate, a semiconductor device using the same and a method of producing the semiconductor material in which a carbon-rich surface is formed on the SiC substrate prior to epitaxial growth of an SiC crystal, the carbon-rich surface satisfies the ratio R = (I284.5/I282.8) >0.2, wherein I282.8 (ISiC) is an integrated intensity of a Cls signal having a peak at the binding energy relating to stoichiometric SiC (in the region of 282.8 eV), and I284.5 (IC) is an integrated intensity of a C1s signal having a peak at the binding energy relating to graphite, SiCx (x>1), or SiyCH1-y (y<1) (in the region of 284,5 eV), as measured by an X-ray photoelectron spectroscopic analyzer (XPS). |
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149 | Silver halide color photographic materials and processing method | EP88110099.4 | 1988-06-24 | EP0296606A2 | 1988-12-28 | Yamagami, Hiroyuki Fuji Photo Film Co., Ltd.; Aida, Shunichi Fuji Photo Film Co., Ltd. |
A silver halide color photographic material comprising at least one layer of, respectively, a blue-sensitive silver halide emulsion layer containing a yellow color coupler, a green-sensitive silver halide emulsion layer containing a magenta color coupler, and a red-sensitive silver halide emulsion layer containing a cyan color coupler, on a support; |
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150 | Method of making activated carbon bodies having improved adsorption properties | US09231860 | 1999-01-14 | US06187713B1 | 2001-02-13 | Kishor P. Gadkaree |
An activated carbon body and method of making the body which involves providing an inorganic substrate, thermosetting resin, and an adsorption enhancing additive which can be sulfur and/or oil which is non-miscible with and non-reactive with the carbon precursor, contacting the inorganic substrate with the carbon precursor and the adsorption enhancing additive to coat the substrate therewith, curing and carbonizing the carbon precursor, and activating the carbon to produce a coating of activated carbon on the substrate and form the activated carbon body. Another method involves forming a mixture of thermosetting resin, adsorption enhancing additive, which can be sulfur, phosphoric acid, and/or the oil, temporary organic binder, optional forming aid, and fillers, shaping the mixture into a body, followed by curing, carbonizing, and activating to produce a shaped body of activated carbon. When sulfur is utilized, a sulfur-carbon bond forms that is characterized by a peak at 165.9 eV when analyzed by Electron Spectroscopy for Chemical Analysis. | ||||||
151 | Catalysts and processes for formaldehyde-free durable press finishing of cotton textiles with polycarboxylic acids, and textiles made therewith | US570489 | 1990-08-21 | US5221285A | 1993-06-22 | Bethlehem K. Andrews; Nancy M. Morris; Darrell J. Donaldson; Clark M. Welch |
Catalysts for the rapid esterification and crosslinking of fibrous cellulose in textile form by polycarboxylic acids at elevated temperatures are disclosed. The catalysts are acidic or weakly basic salts selected from the alkali metal dihydrogen phosphates and alkali metal salts of phosphorous, hypophosphorous, and polyphosphoric acids. Suitable polycarboxylic acids include saturated, unsaturated and aromatic acids, as well as alpha-hydroxy acids. The textiles so treated exhibit high levels of wrinkle resistance and smooth drying properties durable to repeated laundering in alkaline detergents, and do not contain or release formaldehyde. Textiles treated by the polycarboxylic acids and alkali metal phosphite or hypophosphite catalysts, and having residues of these catalysts present, may be identified by infrared spectroscopy and electron spectroscopy for chemical analysis, because these textiles exhibit the presence in infrared spectra of the phosphorus-hydrogen bond and the ester groups of cellulose crosslinked with the polycarboxylic acids, and the presence of trivalent phosphorus in spectra from electron spectroscopy for chemical analysis. | ||||||
152 | Toner for developing latent electrostatic images | US912567 | 1992-07-13 | US5244765A | 1993-09-14 | Koichi Katoh; Masami Tomita; Tomoe Hagiwara |
A toner for developing latent electrostatic images which comprises a binder resin comprising a styrene polymer or a copolymer thereof, a releasing agent, dispersed in the above binder resin, comprising a low-molecular-weight polypropylene with a weight-average molecular weight of 3000 to 25000, and a coloring agent, dispersed in the above binder resin, with the styrene polymer or copolymer thereof being contained in a ratio of 10-50% and the low-molecular-weight polypropylene in a ratio of 5-60% at a surface portion of the above toner measured by the electron spectroscopy for chemical analysis (ESCA), and a maximum particle diameter of the low-molecular-weight polypropylene contained in the releasing agent being 5000 .ANG. or less. | ||||||
153 | Method of forming epitaxial SiC using XPS characterization | US11586680 | 2006-10-26 | US07678671B2 | 2010-03-16 | Akinori Seki; Yukari Tani; Noriyoshi Shibata |
A semiconductor material having a stepwise surface structure of (0001)-plane terraces and (11-2n)-plane steps [n≧0] on the SiC substrate, a semiconductor device using the same and a method of producing the semiconductor material in which a carbon-rich surface is formed on the SiC substrate prior to epitaxial growth of an SiC crystal, the carbon-rich surface satisfies the ratio R=(I284.5/I282.8)>0.2, wherein I282.8 (ISiC) is an integrated intensity of a C1s signal having a peak at the binding energy relating to stoichiometric SiC (in the region of 282.8 eV), and I284.5 (IC) is an integrated intensity of a C1s signal having a peak at the binding energy relating to graphite, SiCx (x>1), or SiyCH1-y (y<1) (in the region of 284.5 eV), as measured by an X-ray photoelectron spectroscopic analyzer (XPS). | ||||||
154 | Liquid crystal cell and its manufacturing method | US50058 | 1998-03-30 | US5861932A | 1999-01-19 | Masashi Inata; Kahoru Mori; Katsuhiro Suzuki; Akiji Higuchi |
A pair of electrode panels are supported by plural spacer walls made of photo-resist resin to form a cell gap between electrode panels. The cell gap is filled with liquid crystal, preferably, antiferroelectric liquid crystal. The spacer walls are formed on an orientation layer formed on either panel. A thin layer is also formed on the orientation layer together with formation of the spacer walls as a residual layer. The residual layer has to be sufficiently thin not to disturb orientation of the liquid crystal and to attain a sufficiently high display contrast. The thickness of the residual layer is indirectly detected by an X-ray electron spectroscopy for chemical analysis (ESCA), and the residual layer is made sufficiently thin by setting a temperature of a preliminary baking process, which is carried out before formation of the spacer walls, in a proper range. | ||||||
155 | Surface modification of solid phase objects by poly(vinyl alcohol) | US10162445 | 2002-06-03 | US07179506B2 | 2007-02-20 | Wei Chen |
The adsorption of poly(vinyl alcohol) (PVOH) from aqueous solution to hydrophobic solid-phase objects with varying chemical compositions, sizes, and geometries, is assessed as a new approach for surface modification. The effects of PVOH concentration, adsorption kinetics, PVOH molecular weight, adsorption temperature, solution ionic strength and stepwise deposition on wettability and adsorbed amounts were analyzed by water contact angle and X-ray Photoelectron Spectroscopy. PVOH adsorbs to solids significantly different than do other molecules. A much larger adsorbed amount and more dramatic improvement of wettability occurs compared to other molecules. The low solubility of PVOH, the strong tendency for it to crystallize at the solid/water interface and stabilization of the PVOH film by inter- and intra-molecular hydrogen bonding give additional driving forces for adsorption. The available —OH group from adsorbed PVOH is a versatile functional group and is further chemically transformed to a range of other functional groups to impart desired surface properties. | ||||||
156 | Surface modification of solid phase objects by poly(vinyl alcohol) | US10162445 | 2002-06-03 | US20030091750A1 | 2003-05-15 | Wei Chen |
The adsorption of poly(vinyl alcohol) (PVOH) from aqueous solution to hydrophobic solid-phase objects with varying chemical compositions, sizes, and geometries, is assessed as a new approach for surface modification. The effects of PVOH concentration, adsorption kinetics, PVOH molecular weight, adsorption temperature, solution ionic strength and stepwise deposition on wettability and adsorbed amounts were analyzed by water contact angle and X-ray Photoelectron Spectroscopy. PVOH adsorbs to solids significantly different than do other molecules. A much larger adsorbed amount and more dramatic improvement of wettability occurs compared to other molecules. The low solubility of PVOH, the strong tendency for it to crystallize at the solid/water interface and stabilization of the PVOH film by inter- and intra-molecular hydrogen bonding give additional driving forces for adsorption. The available-OH group from adsorbed PVOH is a versatile functional group and is further chemically transformed to a range of other functional groups to impart desired surface properties. | ||||||
157 | Surface-coated cermet cutting tool with hard coating layer having excellend chipping resistance | EP04106794.3 | 2004-12-21 | EP1548154A2 | 2005-06-29 | Hayahi, Takuya Mitsubishi Materials Corp.; Osikai, Takatoshi Mitsubishi Materials Corp.; Tsushima, Fumio Mitsubishi Materials Corp. |
There is provided a surface-coated cermet cutting tool with a hard-coating layer having excellent chipping resistance. The surface-coated cermet cutting tool is formed by coating, on a surface of a tool substrate made of WC-based cemented carbide or TiCN-based cermet, a hard-coating layer including the following upper and lower layers (a) and (b): (a) as the lower layer, a Ti compound layer having at least one or two of a TiC layer, a TiN layer, a TiCN layer, a TiCO layer and a TiCNO layer, all of which are deposited by chemical vapor deposition, the titanium compound layer having a total average thickness of 3 to 20 µm, and (b) as the upper layer, a heat-transformed α-type Al oxide layer formed by carrying out a heat-transforming treatment in a state that titanium oxide particulates satisfying the composition formula: TiOY, (where value Y is 1.2 to 1.9 in an atomic ratio to Ti when measured by Auger Electron Spectroscopy) and chemically deposited as a transformation starting material are dispersedly distributed on a surface of an Al oxide layer having a κ-type or θ-type crystal structure deposited by chemical vapor deposition and satisfying the composition formula: (Al1-XZrX)2O3 (where value X is 0.003 to 0.05 in an atomic ratio when measured by an electron probe micro-analyzer (EPMA)) to thereby transform the crystal structure of the Al oxide layer having the κ-type or θ-type crystal structure into an α-type crystal structure, the heat-transformed α-type Al oxide layer having an average thickness of 1 to 15 µm. |
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158 | Process for producing laminated film and laminated sheet | EP94306893.2 | 1994-09-21 | EP0644032A3 | 1995-04-26 | Hayashida, Haruo; Ishibashi, Fumio; Kubo, Kohji.; Takahata, Hiroaki; Gotoh, Yuji |
A process for producing an extrusion laminated film or sheet is disclosed, which process uses no chemical primer and comprises a plastic substrate and a resin for extrusion laminating which process uses no chemical primer and comprises:
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159 | Surface-coated cermet cutting tool with hard coating layer having excellent chipping resistance | US11019656 | 2004-12-21 | US20050164042A1 | 2005-07-28 | Takuya Hayahi; Fumio Tsushima; Takatoshi Oshika |
There is provided a surface-coated cermet cutting tool with a hard-coating layer having excellent chipping resistance. The surface-coated cermet cutting tool is formed by coating, on a surface of a tool substrate made of WC-based cemented carbide or TiCN-based cermet, a hard-coating layer including the following upper and lower layers (a) and (b): (a) as the lower layer, a Ti compound layer having at least one or two of a TiC layer, a TiN layer, a TiCN layer, a TICO layer and a TICNO layer, all of which are deposited by chemical vapor deposition, the titanium compound layer having a total average thickness of 3 to 20 μm, and (b) as the upper layer, a heat-transformed α-type Al oxide layer formed by carrying out a heat-transforming treatment in a state that titanium oxide particulates satisfying the composition formula: TiOY, (where value Y is 1.2 to 1.9 in an atomic ratio to Ti when measured by Auger Electron Spectroscopy) and chemically deposited as a transformation starting material are dispersedly distributed on a surface of an Al oxide layer having a κ-type or θ-type crystal structure deposited by chemical vapor deposition and satisfying the composition formula: (Al1−XZrX)2O3 (where value X is 0.003 to 0.05 in an atomic ratio when measured by an electron probe micro-analyzer (EPMA)) to thereby transform the crystal structure of the Al oxide layer having the κ-type or θ-type crystal structure into an α-type crystal structure, the heat-transformed α-type Al oxide layer having an average thickness of 1 to 15 μm. | ||||||
160 | Surface-coated cermet cutting tool with hard coating layer having excellent chipping resistance | US11019656 | 2004-12-21 | US07273665B2 | 2007-09-25 | Takuya Hayahi; Fumio Tsushima; Takatoshi Oshika |
There is provided a surface-coated cermet cutting tool with a hard-coating layer having excellent chipping resistance. The surface-coated cermet cutting tool is formed by coating, on a surface of a tool substrate made of WC-based cemented carbide or TiCN-based cermet, a hard-coating layer including the following upper and lower layers (a) and (b): (a) as the lower layer, a Ti compound layer having at least one or two of a TiC layer, a TiN layer, a TiCN layer, a TiCO layer and a TiCNO layer, all of which are deposited by chemical vapor deposition, the titanium compound layer having a total average thickness of 3 to 20 μm, and (b) as the upper layer, a heat-transformed α-type Al oxide layer formed by carrying out a heat-transforming treatment in a state that titanium oxide particulates satisfying the composition formula: TiOY, (where value Y is 1.2 to 1.9 in an atomic ratio to Ti when measured by Auger Electron Spectroscopy) and chemically deposited as a transformation starting material are dispersedly distributed on a surface of an Al oxide layer having a κ-type or θ-type crystal structure deposited by chemical vapor deposition and satisfying the composition formula: (Al1-XZrX)2O3 (where value X is 0.003 to 0.05 in an atomic ratio when measured by an electron probe micro-analyzer (EPMA)) to thereby transform the crystal structure of the Al oxide layer having the κ-type or θ-type crystal structure into an α-type crystal structure, the heat-transformed α-type Al oxide layer having an average thickness of 1 to 15 μm. |