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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
21	Artificial fiber and process of making same	US70102924	1924-03-22	US1695643A	1928-12-18	CARLETON ELLIS

22		JP30588689	1989-11-25	JP2587706B2	1997-03-05	TAKAI YOSUKE; SANO TOYOHIKO

23		JP1391587	1987-01-23	JP2577732B2	1997-02-05	ANSONII JOSEFU BERU

24	JPS599658B2 -	JP16401380	1980-11-20	JPS599658B2	1984-03-03	EMANUERU JII KONTOSU

25	NONWOVEN FABRIC COMPRISING 1*22POLYBUTADIENE	JP16401380	1980-11-20	JPS56123442A	1981-09-28	EMANUERU JII KONTOSU

26		JP6736571	1971-09-03	JPS4833119A	1973-05-08

27	Permselective hollow fiber membrane and blood treatment instrument using the same	JP2003009310	2003-01-17	JP2004216328A	2004-08-05	KAMISAKA TSUTOMU; TERADA RYOZO; SUGAYA HIROYUKI
PROBLEM TO BE SOLVED: To provide a permselective hollow fiber membrane having high permeability and adsorption performance. SOLUTION: The permselective hollow fiber membrane has an asymmetric structure provided with a dense layer on the inside layer and a porous structure on the outside layer and consists essentially of an acrylic resin. The blood treatment instrument is constituted so as to use the same. COPYRIGHT: (C)2004,JPO&NCIPI
28		JP31371690	1990-11-19	JP2522601B2	1996-08-07	TAKAI YOSUKE

29		JP4366190	1990-02-22	JP2521171B2	1996-07-31	TAKAI YOSUKE; KAWANAKA AKIHIKO; KONDO ATSUSHI

30	CONJUGATED YARN AND NONWOVEN FABRIC THEREOF	JP30588689	1989-11-25	JPH03167313A	1991-07-19	TAKAI YOSUKE; SANO TOYOHIKO
PURPOSE:To obtain conjugated yarn useful as nonwoven fabric, having high dynamic friction resistance, comprising a first component of syndiotactic polybutadiene having a specific melting point and a second component of PP, having a ratio of sectional area of the first component to the second component in a specific ratio. CONSTITUTION:The objective yarn comprising a first component of syndiotactic 1,2-polybutadiene having 75-150 deg.C, preferably 80-110 deg.C melting point T deg.C and a second component of PP (preferably one having 150-165 deg.C melting point and 30-70g/10 minutes melt index and having a ratio of sectional area of the first component to the second component of (30:70)-(70:30) wherein the first component occupies >=30% surface area.
31	GLOVE	JP26518489	1989-10-13	JPH03130402A	1991-06-04	IKEDA MASATAKA; SHOJI KOICHI
PURPOSE:To provide working or sports gloves made of a hydrogenated diene block copolymer and a polyolefin at a specific ratio, having excellent elongation, elongation recovery and softness, comfortably fittable to hand and having excellent form stability. CONSTITUTION:The objective gloves are made of a nonwoven cloth having an average fiber diameter of 0.5-30mum and an areal weight of 30-200g/m<2> and produced by compounding (A) 100-65wt.% of a hydrogenated block copolymer obtained by hydrogenating a block copolymer having (i) >=2 block polymers composed mainly of vinyl aromatic compound (e.g. styrene) and (ii) >=2 block polymers composed mainly of conjugated diene compound using titanocene compound, etc., and (B) 0-35wt.% (preferably 5-30wt.%) of a polyolefin (e.g. block copolymer of propylene and ethylene).
32		JP5993775	1975-05-20	JPS5340212B2	1978-10-26

33		JP2854673	1973-03-13	JPS49116325A	1974-11-07

34	Ion exchange fibers and method for manufacturing the same	EP91119365.4	1991-11-13	EP0486934A3	1992-12-09	Takai, Yousuke
Ion exchange fibers comprising a polymer component having a main chain of a syndiotactic poly(1,2-butadiene) structure and containing ion exchange functional groups introduced at least part of side chain ethylene groups. These fibers may be suitably formed into a non-woven fabrics, and thus an ion exchange cloth can be obtained, which has excellent ion exchange capacity, flexiblity excellent processing capacity, high mechanical strength and elongation. The ion exchange fibers have excellent ion exchange capacity with respect to fluid such as water or gas and thus can be used as cartridge filters and fiber-filled filters.
35	Ion exchange fibers and method for manufacturing the same	EP91119365.4	1991-11-13	EP0486934B1	1998-07-15	Takai, Yousuke

36	Method for manufacturing sheath-core ion exchange fibers	US99568	1993-07-30	US5356572A	1994-10-18	Yousuke Takai
Ion exchange fibers including a polymer component having a main chain of a syndiotactic poly(1,2-butadiene) structure and containing ion exchange functional groups introduced at least part of side chain ethylene groups. These fibers may be suitably formed into a non-woven fabrics, and thus an ion exchange cloth can be obtained, which has excellent ion exchange capacity, flexiblity excellent processing capacity, high mechanical strength and elongation. The ion exchange fibers have excellent ion exchange capacity with respect to fluid such as water or gas and thus can be used as cartridge filters and fiber-filled filters.
37	Stabilized reaction products of rubbery polymers with inorganic acidifying compounds	US8980149	1949-04-26	US2654679A	1953-10-06	MICHAEL GOPPEL JOHAN; ERNST RUMSCHEIDT GOTTFRIED; THOMAS HACKMANN JOHANNES
Reaction products of polydienes with sulphur dioxide are stabilized by contacting them with solutions of compounds containing the group C-NRR1 or =C=NR11, in which R, R1 and R11 are hydrogen or the same or different hydrocarbon radicals, the hydrogen atoms of which may be substituted by other atoms or radicals, the presence of oxidizing nitrogen-oxygen radicals in the compounds being avoided. The polydienes are unsaturated polymers, copolymers of conjugated dienes of 4 to 6 carbon atoms and have a molecular weight above 5000. Examples are polymers of butadiene, pentadiene, methyl and dimethyl butadienes, copolymers of mixtures of these and of one or more with alkenes, e.g. isobutene, or vinyl compounds, e.g. styrene, vinyl chloride, vinyl esters, acrylic and methacrylic acids, acrylonitrile and methacrylonitrile. Products in which compounds of molecular weight below 5000 are simultaneously reacted with sulphur dioxide, as described in Specification 659,083, are also included. Examples of stabilizers are aliphatic and aromatic primary, secondary and tertiary amines, e.g. heptadecyl and octadecyl amines, a -naphthylamine, p-phenylene diamine-benzidene, triamino benzene, cetyl aniline, diphenylamine, N - phenyl - b - naphthylamine, methyl tert.-amyl aniline, ethyl butyl and ethyl octyl aniline, ethyl cyclohexyl aniline, triphenylamine; amino acids and elcohols, e.g. triethanolamine; acid amides, e.g. acetamide, stearic acid amide, benzamide, acetanilide; urea, N,N- and N,N1-diphenyl urea, thiourea, N,N- and N,N1-diphenyl thiourea, N,N- and N,N1-diphenyl guanidine; amides of dithio acids, e.g. tetramethyl thiuram disulphide; zinc dimethyl dithiocarbamate; amidines; urethanes and thiourethanes; carbo-di-imides, e.g. diphenyl and diallyl carbo-di-imides, p,p1-dimethyl diamino diphenyl carbo-di-imide; heterocyclic nitrogen compounds, e.g. hexamethylene tetramine, melamine, phenyl melamine, (methyl-2-dodecyl)-pyridine, thiazole, mercapto-benzimidazole; halogen amines, e.g. monochlorurea, quinone dichlorimide; dicyanodiamide; quaternary ammonium compounds, e.g. cetyl pyridinium chloride. In some cases the stabilizers can be used in the form of polymers or copolymers. The stabilizers may be applied by soaking threads or other objects of the reaction product in a stabilizer solution, preferably when the product is still in the swollen state of its production, or it may be added to the liquid in which the product is formed. The stabilizer may also be added to take part in the reaction producing the products, for which purpose compounds containing an alkenyl group are essential. The adhesion may also be improved by heating after application or during incorporation of the stabilizer, and by reacting the stabilized products with compounds such as formaldehyde or iso-cyanates. Combinations of stabilizers may be used, at least two of the group of hexamethylene tetramine and its derivatives, melamine and its derivatives and urea or thiourea and their derivatives including dicyanodiamide, being very effective. The stabilization is against the separation of sulphur dioxide and in some cases is effective against the influence of light. The invention is exemplified with reaction products of rubber and sulphur dioxide.
38	Nonfogging rubber hydrochloride film and method of making it	US10459549	1949-07-13	US2561011A	1951-07-17	CARSON CLARENCE M

39	Process for producing filamentary reaction products of rubbery polymers with sulfur dioxide	US76092447	1947-07-14	US2469847A	1949-05-10	ERNST RUMSCHEIDT GOTTFRIED; DE NIE WILLEM LEENDERT JOHANNE

40	Process for treatment of high molecular weight multiunsaturated polymers of diene hydrocarbons	US31076039	1939-12-23	US2265722A	1941-12-09	DE NIE WILLEM LEENDERT JOHANNE

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