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序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
61 METAL SURFACE TREATMENT AGENT AND METHOD FOR TREATING SURFACE OF METALLIC LAYER JP34280299 1999-12-02 JP2000282033A 2000-10-10 HIUGA HARUFUSA
PROBLEM TO BE SOLVED: To obtain a metal surface treatment agent capable of preventing discoloration of, and improving the soldering wettability, lubricity, contact resistance, etc., on the surface of metallic layers, and thus capable of retaining the surface characteristics of metallic layers over a long period. SOLUTION: This metal surface treatment agent comprises a tetrazole-based compound (a tetrazole compound or mercaptotetrazole compound) and a thiadiazole-based compound (a thiadiazole compound or thidiazolone compound).
62 JP26321291 1991-09-13 JP3054830B2 2000-06-19
63 DEGRADATION INHIBITOR FOR WATER-SOLUBLE POLYMER AND POLYMER FLOCCULANT COMPOSITION CONTAINING SAME JP30150994 1994-11-10 JPH08134257A 1996-05-28 UENO TOSHIHIRO; TAKEBAYASHI SATORU
PURPOSE: To obtain a degradation inhibitor which has no carcinogenicity and is excellent in inhibiting the decrease in mol.wt. of a water-sol. polymer flocculant in a water soln. by using a thiocyanate as the effective component. CONSTITUTION: The degradation inhibitor for a water-sol. polymer contains a thiocyanate as the effective component. Examples of a water-sol. polymer to which the inhibitor is applicable are polyacrylamide, polyethylene oxide, and a urea-formaldehyde condensate. A water-sol. thiocyanate can be used here without any limitation and is exemplified by ammonium thiocyanate, potassium thiocyanate, and barium thiocyanate. The quality degradation of a polymer flocculant is thought to be the decomposition caused by the free-radical chain reaction of an active species, such as an active oxygen species, with the flocculant. The decomposition of the flocculant is thought to be inhibited by the chain transfer of the active species to the inhibitor.
64 SUBSTITUTED 1-AMINONAPHTHALENES AND STABILIZED COMPOSITION JP14094092 1992-05-06 JPH05194331A 1993-08-03 POORU EI ODORISHIO; DEBITSUDO II CHIYASAN; SUTEFUEN DEII PASUTAA
65 DETERIORATION PREVENTIVE AND COMPOSITION CONTAINING THE SAME AND SEMICONDUCTOR DEVICE USING THE COMPOSITION JP666491 1991-01-24 JPH04239597A 1992-08-27 UEMATSU TOYOHITO; KOMATSUZAKI SHIGEKI
PURPOSE:To improve the thermal oxidation stability of the title composition containing a thermally conductive agent in the form of lubricating oil, grease or paste. CONSTITUTION:A pasty thermally conductive agent 4 for improving the heat transfer between a cooling jacket 1 and intermediate thermally conductive block 2, or between said block 2 and semiconductor chip 3 in the cooling structure of a semiconductor device is a composition containing a deterioration preventive made up of (A) a dithiocarbamic acid metal salt and/or xanthogenic acid metal salt and (B) a hindered phenol compound. Synergistic effect of the components A and B will improve the thermal oxidation stability of the composition.
66 THIOESTER JP23047991 1991-09-10 JPH04234484A 1992-08-24 BATSUDO HAABII SUTAAMU; JIYOSEFU ANDORIYUU KUTSUKOUSUK
67 JP33087 1987-01-05 JPH0219142B2 1990-04-27 AASAA ETSUCHI UEINSUTEIN
68 ORGANIC COMPOUND JP14461477 1977-12-01 JPS5377031A 1978-07-08 RICHIYAADO ETSUCHI KURAIN
69 JP8377573 1973-07-25 JPS5034003A 1975-04-02
70 SOLUTION ABSORBANTE CONTENANT UN INHIBITEUR DE DÉGRADATION DÉRIVÉ DU THIADIAZOLE ET MÉTHODE POUR LIMITER LA DÉGRADATION D'UNE SOLUTION ABSORBANTE PCT/FR2009/000775 2009-06-23 WO2009156619A2 2009-12-30 CARRETTE, Pierre-Louis; DELFORT, Bruno

La dégradation d'une solution absorbante comportant des composés organiques munis d'une fonction aminé en solution aqueuse est sensiblement réduite en présence d'une faible quantité d'agents inhibiteurs de dégradation dérivés du thiadiazole définis par la formule générale : (I) La solution absorbante est mise en oeuvre pour désacidifier un effluent gazeux.

71 酸化防止剤及びそれを含有する潤滑油組成物 PCT/JP2005/019210 2005-10-19 WO2006043596A1 2006-04-27 八木下 和宏; 石田 ▲昇▼

 本発明の酸化防止剤は、遷移金属化合物と芳香族化合物との反応物であって、遷移金属原子と芳香族環とが、該芳香族環及び/又はその置換基を構成する硫黄原子、酸素原子又は窒素原子を介して結合した構造を有するものであり、ZDTPやMoDTC等の従来の酸化防止剤と比較して、酸化防止性、更にはNOxに対する耐性及び高温清浄性の点で非常に優れている。したがって、本発明の酸化防止剤を潤滑油に含有せしめることによって、高準のロングドレイン性を潤滑油に付与することが可能となる。

72 LOW TOXICITY CORROSION INHIBITOR PCT/US1998/009225 1998-05-06 WO98051902A1 1998-11-19
A water soluble corrosion inhibitor containing a compound having at least one five-membered heterocyclic ring having at least one thione group and at least one other pendant group is described. Such a corrosion inhibiting compound can be made by reacting together a thiourea and a polyalkylene polyamine. A specific example includes preparing 1-(2-aminoethyl)-2-imidazolidinethione by reacting thiourea, per se, and diethylenetriamine. These corrosion inhibition compounds have greatly reduced aquatic toxicity, and may be employed as corrosion inhibitors in hydrocarbon streams.
73 Organic-based heat stabilizers and heat-stable polymer composition JP2003059052 2003-03-05 JP3928862B2 2007-06-13 ジーン・ケリー・ノリス; トッド・チャールズ・デュバル; ポール・ブライアン・アダムス
74 JP2001167406 2001-06-01 JP3815548B2 2006-08-30
75 Shelf stability improver for ink jet recording medium, ink jet recording medium using this improver and its manufacturing method JP2002327016 2002-11-11 JP2004160734A 2004-06-10 KAWAKAMI TETSUO; YAMAMOTO RYUICHI
PROBLEM TO BE SOLVED: To provide a shelf stability improver for an ink jet recording medium which improves the ink absorption, print density and clarity of the medium by adding the former to the latter; eliminates ink discoloration or fading even after the long-term keeping of printed matter on account of the superb light resistance and resistance to qualitative deterioration by an oxidative gas of the improver; and helps retain successful printability and ameliorate the drying of a coating liquid, and an ink jet recording medium using the improver and its manufacturing method. SOLUTION: The shelf stability improver for an ink jet recording medium contains or adsorbs an inhibitor for qualitative deterioration by an oxidative gas in a copolymer fine particle and/or the surface of the copolymer fine particle obtained by emulsion-polymerizing at least one kind of an ultraviolet absorbing monomer (a) selected between a benzophenone-type ultraviolet absorbing monomer represented by formula (1) and a benzotriazole-type ultraviolet absorbing monomer represented by formula (2) and a vinyl monomer (b) which is copolymerizable with (a). COPYRIGHT: (C)2004,JPO
76 ADDITIVE FOR ORGANIC MATERIAL, ORGANIC MATERIAL COMPOSITION AND NEW COMPOUND JP2001167406 2001-06-01 JP2002363556A 2002-12-18 YOKOO YOSHIO
PROBLEM TO BE SOLVED: To provide an additive of a new compound effective as the additive which can give resistance to oxidative degradation and ozone degradation of an organic material even in a small amount, and an organic material composition. SOLUTION: A hydrazine derivative (except an N, N'-diphenylhydrazine derivative) of formula I (wherein R<1> -R<4> are independently selected each from a 1-30C straight chain or branched alkyl group, a 1-30C alkenyl group, a 3-10C cycloalkyl group, a 6-10C aryl group, a 3-14 membered heterocyclic group, -SO2 -R<5> , -N=NH or hydrogen, and two or more of R<1> -R<4> are each an aryl group) wherein two or more hydrogen atoms of the hydrazine and substituted with an aryl group, an additive for an organic material containing this hydrazine derivative, an organic material and a composition.
77 OXIDATION STABLE LIQUID COMPOSITION JP15376798 1998-05-18 JPH11323329A 1999-11-26 KITAHATA KOICHI; SAKANAKA SENJI; MITSUYA TAKAYUKI
PROBLEM TO BE SOLVED: To provide a liquid composition with little bitter-taste, improved in safety and oxidative stability by adding thereto egg yolk protein hydrolyzates and materials being subject to oxidative degradation thereto. SOLUTION: Egg yolk protein hydrolyzates are prepared by extraction removing lipid from egg yolks to obtain egg yolk proteins, adding enzyme of 1-5 wt.% to the resulting proteins to subject them to an enzyme reaction for 4-24 hr, thereafter if necessary, regulating the pH of the resultant to 6-8, removing insolubles and then subjecting the enzyme to deactivation, art aminoacid composition of said egg yolk proteins comprising Thr of 4-6%, Tyr of 3-5%, Phe of 3-5%, Cys of 1-3%, Met of 2-4%, Val of 5-7%, Ile of 4-6%, Leu of 8-10%, Lys of 6-8%, Trp of 0.5-2.5% and His of 1-3%. To this egg yolk protein hydrolyzates, are added 0.001-0.1% of one or more materials selected from fats and oils containing unsaturated aliphatic acids, vitamins, coloring matters, kinds of perfume and spices, said materials being subject to oxidative degradation.
78 NEW COMPOUND CONTAINING SULFUR AND ITS PRODUCTION JP10755198 1998-04-17 JPH11302255A 1999-11-02 IKEDA KATSUYA; YOSHIDA KATSUHIKO; SUZUKI MICHIO; HATA HIROYUKI
PROBLEM TO BE SOLVED: To obtain a new compound useful as lubricating oil, an additive for the same, grease, an antioxidant, or the like, which are excellent in oxidation stability and thermal stability, and capable of being synthesized from an easily available raw material, by reacting easily available 2,6-dihalopyridine with benzenethiol. SOLUTION: This compound is expressed by formula I [wherein, R<1> and R<2> are each a halogen or a 1-24C hydrocarbon; (m) and (n) are each 0-5], e.g. 2,6-diphenylthiopyridine. The compound of formula I is obtained by reacting 2,6-dihalopyridine of formula II with benzenethiols of formula III and formula IV pref. in the presence of a base. The compound of formula II is easily obtained by the halogenation of pyridine. It is preferable that the compound of formula II is 2,6-dichloropyridine or the like, a sort of benzenethiols is benzenethiol or the like, a base is sodium methylate or the like and the reaction temperature is 100-200 deg.C.
79 METHOD AND APPARATUS FOR STERILIZATION USING VAPOR OF ISOTHIOCYANIC ACID ESTER JP462499 1999-01-11 JPH11292722A 1999-10-26 OHAMA CHIAKI; KATO KEISUKE
PROBLEM TO BE SOLVED: To provide both a method for sterilizing various kinds of articles by using the vapor of an isothiocyanic acid ester (ISOTC) and an apparatus for sterilization using ISOTC. SOLUTION: An article packed with a material having vapor permeability of ISOTC is brought into contact with the vapor of ISOTC. The method comprises a process for introducing ISOTC in a vapor state or a fine particulate state of liquid clroplet into a sterilization chamber to form an atmosphere containing the vapor of ISOTC in the sterilization chamber, a process for sending the article to the sterilization chamber, a process for bringing the article into contact with an atmosphere gas containing ISOTC in the sterilization chamber to sterilize the article, a process for discharging the atmosphere gas in the sterilization chamber after the sterilization and a process for removing the vapor of ISOTC contained in the removed gas.
80 JP3538791 1991-02-05 JP2887700B2 1999-04-26 HANSUURUDORUFU MAIERU; RITA PITSUTERODO
Sulphoxides of bis- and tris-thiomethylated phenols of the formula I or II …… in which …… R1 denotes hydrogen, C1-C18-alkyl, cyclohexyl or C7-C9-phenylalkyl, … R2 and R3, independently of one another, represent hydrogen or methyl, … R4 represents C4-C18-alkyl, phenyl, C7-C9-phenylalkyl, C1-C4-alkyl-substituted phenyl, hydroxyethyl or a radical -(CH2)rCOOR5, in which r represents 1 or 2 and R5 denotes C1-C18-alkyl, … Z represents sulphur, ……… in which R2 and R3 have the abovementioned meaning, or represents a direct bond, and n, m and p, independently of one another denote the value 0 or 1, and mixtures thereof with the corresponding non-oxidised compounds are suitable as stabilisers for materials which are sensitive to oxidative, thermal and/or light-induced degradation.