序号 | 专利名 | 申请号 | 申请日 | 公开(公告)号 | 公开(公告)日 | 发明人 |
---|---|---|---|---|---|---|
121 | Aliphatic, low-emission thermoplastic polyurethane molding materials suitable for sintering | US09581771 | 2000-06-16 | US06420510B1 | 2002-07-16 | Wolfgang Kaufhold; Hans-Georg Hoppe; Herbert Heidingsfeld; Rainer Ohlinger; Michael Kalbe |
Polyurethane moulding compositions which can be melt processed in the form of sintering powders suitable for the preparation of grained sintered films and which are prepared exclusively from linear aliphatic components are described. The polyol component is composed of 30 to 80 parts by weight of an aliphatic polycarbonate diol with an average molecular weight {overscore (M)}n of 1000 to 2200 and 70 to 20 parts by weight of a polybutane diol adipate and/or a polycaprolactone diol with an average molecular weight {overscore (M)}n of 1000 to 2400. Moreover, the mixture contains 1,6-hexamethylene diisocyanate in an equivalence ratio of 2.3:1.0 to 6.2:1.0, based on the polyol mixture and butane-1,4-diol as chain extender, the equivalence ratio of the butane-1,4-diol based on the poly mixture being 1.3:1.0 to 5.2:1.0. | ||||||
122 | POLYURETHANE RESIN TYPE COMPOSITION FOR SLUSH MOLDING | US09406129 | 1999-09-27 | US20020016436A1 | 2002-02-07 | HIDEKI OHMORI; YOSHITSUGU TAKAI; ERIKO TAKAI; JUNZO UKAI; HIDEO NISHIMURA; KAZUO KOBAYASHI; MAHITO NOMURA |
A composition suitable for slush molding is disclosed. The composition comprises a thermoplastic polyurethane elastomer (A) having a number average molecular weight of 10,000 to 50,000 and mainly comprised of a diol component including an aromatic ring-containing diol and a non-aromatic diisocyanate; a plasticizer (B); and optionally an additive. The composition provides a molded article excellent in durability such as thermal/light aging resistance and chemical resistance, soft touch at low temperature, and appearance. | ||||||
123 | Aliphatic sinterable thermoplastic polyurethane moulding compositions of reduced mechanical strength | US225145 | 1999-01-04 | US06166135A | 2000-12-26 | Wolfgang Kaufhold; Hans-Georg Hoppe; Rainer Ohlinger; Michael Kalbe; Hans-Hinrich Kruse |
The invention relates to light-stable sinterable thermoplastic polyurethane molding compositions of reduced mechanical strength which can be processed by the powder-slush process. The molding compositions according to the invention are particular suitable for the production of grained sintered films for interior lining of means of transport, in particular as a covering for airbags in motor vehicles. | ||||||
124 | Thermoplastic polyurethane molding compound for manufacturing grained, sintered, plastic sheet | US14957 | 1993-02-08 | US5541277A | 1996-07-30 | Horst M uhlfeld; Thomas Dabisch; Gerhard M uller-Broll |
A thermoplastic sinterable powder for manufacturing grained, sintered plastic sheet is described, which is comprised 100 party by weight of an exclusively linear, aliphatic polyol mixture composed of 60 to 80 parts by weight of polycarbonate diol, having an MW of 2000 and a hydroxyl value of 56 based on adipic acid, hexane diol and neopentyl glycol, having an MW of 2000 and a hydroxyl value of 56. Also included is 1,6-hexamethylene diisocyanate in an equivalence ratio of about 2.8:1.0 to 4.2:1.0, with respect to the total polyol, with the exception of 1,4-butane diol which is added as a chain lengthener. The coefficient of the molding compound, calculated from the quotient of the equivalence ratios of the isocyanate groups multiplied by 100 and the sum of the hydroxyl groups of polyols and chain lengtheners is in the range of about 97 to 99. | ||||||
125 | Preparation of solid polyurethane particles | US413294 | 1982-08-31 | US4403083A | 1983-09-06 | Nelson S. Marans; Clifton L. Kehr |
This invention relates to novel hydrophilic, crosslinked, polyurea-urethane, solid, discrete particles formed by adding in droplet form a hydrophilic prepolymer comprising an isocyanate-capped polyol or mixtures thereof wherein said polyol or mixture of polyols has a reaction functionality greater than two, the total of said polyol present having an ethylene oxide content of at least 40 weight percent, before capping to a large excess of a stirred aqueous reactant. The resultant solid particles can be molded into various shapes as desired or used for coating or adhesive applications. | ||||||
126 | Process for the production of organic alkali metal silicate compounds | US329283 | 1981-12-10 | US4354019A | 1982-10-12 | David H. Blount |
An oxidated silicon compound will react with a substituted organic compound in the presence of an alkali compound to produce organic alkali metal silicate products which may be used as molding powders, as adhesives, as coating agents and be reacted with polyisocyanates to produce insulating foams. | ||||||
127 | Process for the production of alkali metal silicate-organic plastics | US359609 | 1982-03-18 | US4353999A | 1982-10-12 | David H. Blount |
Polymerable organic compounds and an epoxide compound are emulsified with aqueous alkali metal silicate solutions then polymerized with a catalyst such as a peroxide type catalyst thereby producing an alkali metal silicate organic plastic which may be used as an adhesive, as molding powder or reacted with an organic diisocyanide to produce polyurethane silicate resins and foams. | ||||||
128 | Process for the production of organic alkali metal silicate compounds | US328198 | 1981-12-07 | US4346192A | 1982-08-24 | David H. Blount |
An oxidated silicon compound will react with a substituted organic compound in the presence of an alkali compound to produce organic alkali metal silicate products which may be used as molding powders, as adhesives, as coating agents and be reacted with polyisocyanates to produce insulating foams. | ||||||
129 | Process for the production of organic alkali metal silicate compounds | US329405 | 1981-12-10 | US4346180A | 1982-08-24 | David H. Blount |
An oxidated silicon compound will react with a substituted organic compound in the presence of an alkali compound to produce organic alkali metal silicate products which may be used as molding powders, as adhesives, as coating agents and be reacted with polyisocyanates to produce insulating foams. | ||||||
130 | Process for the production of organic alkali metal silicate compounds | US251132 | 1981-04-06 | US4321184A | 1982-03-23 | David H. Blount |
An oxidated silicon compound will react with a substituted organic compound in the presence of an alkali compound to produce organic alkali metal silicate products which may be used as molding powders, as adhesives, as coating agents and be reacted with polyisocyanates to produce insulating foams. | ||||||
131 | Thermoplastic polyurethane elastomers from polyoxypropylene polyoxyethylene block copolymers | US572741 | 1975-04-29 | US4202957A | 1980-05-13 | Henry W. Bonk; Tilak M. Shah |
Polyurethane polyether-based elastomers are described which are thermoplastic, recyclable and have increased high temperature resistance which permits fabrication by injection molding. The elastomers are the product of reaction of 4,4'-methylenebis(phenyl isocyanate), a particular group of polypropylene oxide-polyethylene oxide block copolymers and an extender [straight chain aliphatic diols C.sub.2-6 or the bis(2-hydroxyethyl ether) of hydroquinone or resorcinol]. The block copolymers have at least 50 percent primary hydroxyl groups, a pH in the range of 4.5 to 9, a content of alkali metal ion less than 25 ppm and a molecular weight of 1000 to 3000. The minimum ethylene oxide (E.O.) residue content (percent by weight) of the polyether for any molecular weight (M.W.) is governed by the equation: ##EQU1## In a particularly preferred embodiment the elastomers are prepared by replacing up to 25 percent by equivalents of the extender by certain diols (polyethylene glycols up to 1500 M.W. preferred). | ||||||
132 | Solid particle-form polymerizable polymeric material and compositions, structures and methods of employing and producing the same | US460482 | 1974-04-12 | US3947426A | 1976-03-30 | Harry L. Lander |
Solid particle-form, polymerizable or cross-linkable, multi-functional polymeric material containing blocked isocyanate groups wherein the blocked isocyanate groups making up said polymeric material comprise only a portion of the total isocyanate groups to produce said polymeric material, such as extrudable, thermosettable powdered blocked polyurethane (PBP) has been prepared. This material is useful per se for the manufacture of articles and may be added in combination with other materials, such as thermoplastic resins, e.g. polyethylene, polyvinyl chloride, for improving the usefulness, versatility and physical and/or chemical properties thereof. The polymeric material, such as PBP, is useful as a coating on metal and non-metallic surfaces, e.g. glass or fibrous surfaces, either as a protective coating or for the purpose of laminating such surfaces to another surface. The polymeric material, such as PBP, may be manufactured by reacting a liquid reaction admixture comprising a partially blocked polyurethane prepolymer with a chain extending reactant under conditions such that the reaction admixture is reacted in dispersed form with the result that the reaction product is recoverable in solid particle-form as said PBP. | ||||||
133 | Moulding composition | US30133172 | 1972-10-27 | US3907751A | 1975-09-23 | KNIGHT MICHAEL HORACE; MITCHELL BARBARA; RATCLIFFE MAURICE JAMES |
Moulding composition in particulate form comprising at least one prepolymer containing urethane groups and having the structure
and hereinafter referred to as the vinyl-ended prepolymer, in which R1 and R2 are each divalent organic groups at least one of which contains at least one cyclic group in the chain and are such that in said structure there are not more than 20 atoms in the chain between each cyclic group, n is a whole number of from 1 to 20, and when n is one and only R2 contains a cyclic group in the chain there are no more than 20 atoms in the chain between the cyclic group in R2 and the nitrogen atom attached to the group X, R3 is hydrogen or a hydrocarbyl group and X is a divalent group are useful in forming articles such as films. |
||||||
134 | Thermoplastically processable polyurethane elastomers | US3689443D | 1970-11-09 | US3689443A | 1972-09-05 | FENSCH WALTER |
A POLYURETHANE ADAPTED TO BE PROCESSED THERMOPLASTICALLY INTO A PRODUCT HAVING A SUBSTANTIALLY PERMANENT HARDENSS OF ABOUT SHORE A 80* OR LESS IS PROVIDED BY REACTING A HYDROXY POLYCAPROLACTONE HAVING A MOLECULR WEIGHT OF FROM ABOUT 1,500 TO ABOUT 2,500, A HYDROXY POLYCAPROLACTONE HAVING A MOLECULAR WEIGHT OF FROM ABOUT 500 TO ABOUT 600, A GLYCOL HAVING A MOLECULAR WEIGHT BELOW ABOUT 250 AND DIPHENYLEMTHANE-4,4''-DIISOCYANATE.
|
||||||
135 | Thermoset resins with hydroxy acrylate methacrylonitrile and blocked isocyanate | US3660359D | 1970-06-05 | US3660359A | 1972-05-02 | LABANA SANTOKH S |
NOVEL THERMOSETTING RESIN POWDERS WHICH CAN BE MOLDED TO FORM PRODUCTS CHARACTERIZED IN TENSILE MEASUREMENT, BY HIGH ELONGATION-TO-BREAK, HIGH TENSILE STRENGTH AND MODULUS AND A HIGH GLASS TRANSITION TEMPERATURE ARE PREPARED FROM A MIXTURE OF (A) A PREPOLYMER FORMED BY REACTING (1) A HYDROXY ESTER OF ACRYLIC OR METHACRYLIC ACID AND A C2-C3 DIOL WITH (2) METHACRYLONITRILE OR ACRYLONITRILE OR A MIXTURE OF THE SAME, AND (B) BLOCKED DI- OR TRIISOCYANATE WHEREIN THE ISOCYANATE GROUPS ARE DIRECTLY ATTACHED TO AN AROMATIC RING AND DEBLOCK AT TEMPERATURES IN THE RANGE OF 120* TO 160*C.
|
||||||
136 | Thermoset molding powders from hydroxy-functional acrylic rubber particles and monoblocked diisocyanates and molded article | US3660355D | 1970-12-21 | US3660355A | 1972-05-02 | JOHNSON OLIN B; LABANA SANTOKH S |
NOVEL THERMOSETTING RESIN POWDERS WHICH CAN BE MOLDED TO FORM UNIQUE, URETHANE-CROSSLINKED, ELASTOMERCOMPRISING PRODUCTS ARE PREPARED BY REACTING HYDROXYFUNCTIONAL, ELASTOMERIC, ACRYLIC POLYMER PARTICLES WITH A MONOBLOCKED DIISOCYANATE. THESE POWDERS ARE MOLDED BY CONVENTIONAL MOLDING TECHNIQUES TO FORM UNIQUE THERMOSET PRODUCTS.
|
||||||
137 | Thermoset molding powders from hydroxy-functional graded elastomer particles and monoblocked diisocyanate and molded article | US3659003D | 1970-12-21 | US3659003A | 1972-04-25 | JOHNSON OLIN B; LABANA SANTOKH S |
NOVEL THERMOSETTING RESIN POWDERS WHICH CAN BE MOLDED TO FORM UNIQUE, URETHANE-CROSSLINKED, ELASTOMERCOMPRISING PRODUCTS ARE PREPARED BY REACTING HYDROXYFUNCTIONAL, GRADED, ACYRLIC, RUBBER-LIKE PARTICLES WITH A MONOBLOCKED DIISOCYANATE. THESE POWDERS ARE MOLDED BY CONVENTIONAL MOLDING TEHCNIQUES TO FORM UNIQUE THERMOSET PRODUCTS.
|
||||||
138 | Release of agents from adsorbate-containing molecular sieves | US14158961 | 1961-09-29 | US3341488A | 1967-09-12 | O'CONNOR FRANCIS M |
139 | Method of making polyurethanes | US18967862 | 1962-04-24 | US3233025A | 1966-02-01 | FRYE BERNARD F; PIGOTT KENNETH A; SAUNDERS JAMES H |
140 | Homogenized crosslinked polyurethanes | US81430259 | 1959-05-19 | US3192185A | 1965-06-29 | MARVIN ACHTERHOF; FETTERMAN MILES Q; HAVENS NELSON L; MCWHORTER JOHN F |