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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
81 Material for use with a capacitive touch screen US13307681 2011-11-30 US09051621B2 2015-06-09 Gerald Leto
A modified material for use with a capacitive touch screen is described. The modified material comprises a material impregnated with a composition comprising either a non-metallic and/or a metallic conductive agent with a binder. A variety of materials are contemplated, including, but not limited to leather. Also described is an apparatus and method of providing a conductive glove is disclosed.
82 Leather belts or aprons for textile machines US665189 1976-03-09 US4061803A 1977-12-06 Wallace Ronald Brooksbank; David Toft
The invention relates to the production of leather belts and aprons for textile machines in which the natural smooth and relatively non-fibrous grain surface of the leather is removed to expose the natural inner flesh surface and subjecting the surface to mechanical treatment by setting or rolling to compact the surface and impregnating the surface with a polymeric substance to consolidate the surface layer to produce a belt or apron with a smooth non-tacky surface.
83 CULTURED LEATHER AND PRODUCTS MADE THEREFROM US16099130 2017-05-05 US20190144958A1 2019-05-16 Christian EWTON; Michalyn ANDREWS
A cultured leather comprising a plurality of layers each layer comprising cells and extracellular collagen, wherein each layer of the plurality of layers is coupled to an adjacent layer by a nucleotide adhesion molecule, wherein the cultured leather comprises a moisture content of less than 40%.
84 Compounds and their use for producing leather and as dispersants US12377360 2007-08-08 US08211550B2 2012-07-03 Stephan Hüffer; Sebastien Garnier; Oliver Reese; Günter Scherr; Harald Kiesow
A process for the production of leather using one or more reaction products of (a) triamines or higher amines with (b) at least one compound of the general formula I A1-R1  I where R1 is selected from hydrocarbon radicals having 10 to 5000 carbon atoms, straight-chain or branched, saturated or having from one to three C—C double bonds, and A1 from groups capable of reacting with amines.
85 Coating material for covering an airbag, and a method of producing the coating material US10910656 2004-08-03 US20050029777A1 2005-02-10 Ludwig Fleiner
A coating material for covering an airbag in an inner space of a motor vehicle has an area portion adapted to face an airbag, the area portion being formed as a treated portion with a treatment selected from the group consisting of a chemical treatment, a thermal treatment and both, with use of a fluid selected from the group consisting of an alkaline solution, a caustic soda, an acid, a hydrochloric acid, and a combination thereof.
86 Method of manufacturing belts US28909419 1919-04-10 US1360923A 1920-11-30 FELICE GILARDINI
87 MYCELIUM GROWTH BED EP19873847.8 2019-10-18 EP3866579A1 2021-08-25 ROSS, Philp; SCULLIN, Matt; WENNER, Nicholas; CHASE, Jordan; MILLER, Quinn; SALTIDOS, Ryan; MCGAUGHY, Phil
88 CULTURED LEATHER AND PRODUCTS MADE THEREFROM EP17793493.2 2017-05-05 EP3452622A1 2019-03-13 ANDREWS, Michalyn; EWTON, Christian
89 LEDER MIT VERÄNDERUNG DER OBERFLÄCHENFARBE IN ABHÄNGIGKEIT VON DER TEMPERATUR SOWIE VERFAHREN ZU DESSEN HERSTELLUNG EP19186403.2 2019-07-16 EP3617331B1 2023-02-22 Xu, Yanqiu; Liu, Haiyang; Teng, Dayong
90 FUNCTIONALIZING TREATMENT METHOD FOR HIDES EP20797177.1 2020-10-02 EP4038208A1 2022-08-10 NETTI, Paolo Antonio; IANNONE, Maria
91 FUNCTIONALIZING TREATMENT METHOD FOR HIDES PCT/IB2020/059256 2020-10-02 WO2021064669A1 2021-04-08 NETTI, Paolo Antonio; IANNONE, Maria
A functionalizing treatment method for hides and the like that have a surface and an internal substrate that comprises interconnected fibers, which comprises a deposition step (10), in which a plurality of functionalizing elements comprising nanomolecules and/or nanoparticles are inserted into the internal substrate of the hide to be treated, between the individual fibers, so as to coat and functionalize the individual fibers.
92 MYCELIUM GROWTH BED PCT/US2019/057087 2019-10-18 WO2020082043A1 2020-04-23 ROSS, Philp; SCULLIN, Matt; WENNER, Nicholas; CHASE, Jordan; MILLER, Quinn; SALTIDOS, Ryan; MCGAUGHY, Phil

A mycelium growth bed for optimal production of pure mycelium or a pure mycelium composite with controlled or predictable properties, the bed comprising a tray, a conveying platform, a permeable membrane, a substrate, a porous material and a lid. The permeable membrane is positioned on the conveying platform within the tray. The substrate is positioned on the permeable membrane and the porous material is positioned on top of the substrate. The system provides a configuration having a substrate weight to surrounding space volume ratio between 0.5 and 5.0 g/cc, an air volume (surrounding space) to substrate volume between 0.01 and 1.0, and an air volume (surrounding space) to substrate area is between 0.5 and 5 cc/cm, wherein the C02 concentration is held above 3%, the relative humidity is held above 40% and the O2 concentration is held below 20% in steady state conditions to produce leather-like mycelium without fruiting bodies.

93 MYCELIUM GROWTH BED CA3110583 2019-10-18 CA3110583A1 2020-04-23 ROSS PHILP; SCULLIN MATT; WENNER NICHOLAS; CHASE JORDAN; MILLER QUINN; SALTIDOS RYAN; MCGAUGHY PHIL
A mycelium growth bed for optimal production of pure mycelium or a pure mycelium composite with controlled or predictable properties, the bed comprising a tray, a conveying platform, a permeable membrane, a substrate, a porous material and a lid. The permeable membrane is positioned on the conveying platform within the tray. The substrate is positioned on the permeable membrane and the porous material is positioned on top of the substrate. The system provides a configuration having a substrate weight to surrounding space volume ratio between 0.5 and 5.0 g/cc, an air volume (surrounding space) to substrate volume between 0.01 and 1.0, and an air volume (surrounding space) to substrate area is between 0.5 and 5 cc/cm, wherein the C02 concentration is held above 3%, the relative humidity is held above 40% and the O2 concentration is held below 20% in steady state conditions to produce leather-like mycelium without fruiting bodies.
94 DE102006005537 2006-02-07 DE102006005537A1 2007-06-14 CHA YOON-JONG; IM JUN-WAN; AHN SUNG-DUCK
The present invention heats to melt a urethane prepolymer (A ingredient) including a hydroxyl (-OH) functional group in a liquid state or a semi-solid state at room temperature as itself or temperature at 30° C. to 80° C., an isocyanate compound (B ingredient) for reacting with a hydroxyl functional group of urethane prepolymer, a mixture (C ingredient) of a hardening catalyst by cross-link, a pores formation assistance catalyst, a silicone surfactant, and an additive is added by fixed quantity and agitation at high speed to mix. Thus formed porous material of cream shape is using by knife coating process. Thus, the purpose of the present invention is manufacturing a solvent-less urethane porous foamed material fabricating synthetic leather as uniformity of micro pores and good mechanical properties of high strength.
95 Preparation of leather, e.g. for producing clothing or furniture, by treating with new copolymer of unsaturated acid or anhydride, vinyl aromatic compound and alkoxylated unsaturated ether DE10333749 2003-07-23 DE10333749A1 2005-02-10 HUEFFER STEPHAN; WOLF GERHARD; KLUEGLEIN MATTHIAS; BECKER STEFAN
Preparation of leather involves treating unhaired hide, pickled unhaired hide or semi-finished leather with a polymer (A) obtained by copolymerization of: one or more of 3-8C monoethylenically unsaturated mono- or dicarboxylic acids or their anhydrides; vinyl aromatic compound(s); alkoxylated unsaturated ether(s) (I); and optionally further monoethylenically unsaturated monomers. The copolymers (A) are new. Preparation of leather involves treating unhaired hide, pickled unhaired hide or semi-finished leather with a polymer (A) obtained by copolymerization of: (1) one or more of 3-8C monoethylenically unsaturated mono- or dicarboxylic acids or their anhydrides, (2) vinyl aromatic compound(s), (3) alkoxylated unsaturated ether(s) of formula (I) and optionally (4) further monoethylenically unsaturated monomers. [Image] R 1>- R 5>H or Me; R 6>H, SO 3M, PO 3M 2, CHO, (1-20C) alkylcarbonyl or (6-14C) arylcarbonyl; M : alkali metal, NH 4+>or Me; n : 3-100; y : 0-10. Independent claims are included for: (a) the polymers (A) as new; (b) the preparation of (A); and (c) aqueous dispersions containing up to 50 wt. % (A).
96 METHOD OF MANUFACTURING TECHNICAL LEATHER SU4110759 1986-08-13 SU1406174A1 1988-06-30 MIRONOV FLAVIAN V; MAKAROVA ELENA G; ROGOVOJ DAVID E; MUZYCHENKO LEONID N; BAJKINA NINA D
97 METHOD OF TAWING COMMERCIAL LEATHER SU4044465 1986-03-13 SU1326621A1 1987-07-30 MAKAROVA ELENA G; MIRONOV FLAVIAN V; BAJKINA NINA D; YAKUSHEVA GALINA G; VERNOSLOV IGOR B; FEDOROV VALERIJ M; NIKITINA LYUDMILA E; IVANOVA VERA A
98 GB1237929D 1968-11-18 GB1237929A 1971-07-07
1,237,929. Treating leather. FERENTZI KESSLER. Nov. 18, 1968, No.42041/71. Divided out of 1, 237, 928. Heading C6C. Skins to be treated in a liquid bath, e.g. a tanning or degreasing bath as described in the parent specification, are formed into a belt, to facilitate passage through the treating bath, by first cutting them, while the skins are damp, to the shape shown, which cutting involves removal of the lateral recesses (bold flanks) to produce straight tapering side edges, while substantial parts 26 of the hind legs and the head-sections 29 remain, the skins then being arranged side by side and sewn or stuck together such that alternate skins 231, have their head ends facing one way and the other skins 241 are turned through 180 degrees so as to interfit.
99 Process for the treatment of scrap leather GB177549 1949-01-21 GB661196A 1951-11-21
Scrap leather is treated to recover fats and a brown or yellow dye, by digesting the scrap leather with an alkali in an autoclave with steam under pressure, removing the solution obtained and treating it, after separation of liberated fats, with an acid, particularly nitric acid, either (a) for a period of 1 or more hours to obtain after neutralizing a "leather solution," or (b) filtering off the solids obtained, followed by washing, neutralizing and vacuum drying the solids to obtain a brown dye, or (c) treating the "leather solution" obtained as in (a) with further acid, particularly nitric acid, and proceeding as in (b), to obtain a yellow dye, fats being also separated off during or after the acid treatment. In the first stage treatment with alkali, a proportion of water is mixed with the leather scraps, the alkali is either caustic soda or caustic potash, and the temperature, depending on the steam pressure, varies from 250 DEG to 360 DEG F. The treatment is continued with agitation until a neutral or slightly alkaline solution, which is soluble in water, is obtained. In the second stage treatment with acid according to the process (a) above, the solution obtained is fed into glass or enamelled containers equipped with stirring apparatus, allowed to cool to segregate fats which are removed and then treated with the acid whilst stirring for the period specified, the vapours developed being exhausted from the containers. On completion the mass cools, more fat is segregated and is removed, and the solution is then neutralized and filtered to obtain the so-called "leather solution" which is capable of producing a hard filling for leather when dried. In the second stage treatment with acid according to the process (b) above, the solution obtained from the autoclave is filtered and then treated with the acid, which in this case may be H2SO4, when the solids are precipitated which are removed, washed, and dissolved in caustic soda or caustic potash. This solution is then vacuum dried and the solids obtained pulverized to form a brown dye. Preliminary to the first stage of the processes, the scrap leather may be treated in the autoclave with water only and steam under pressure. On cooling, the surface layer of fats may be removed, and the undissolved scrap leather treated as in the main process.ALSO:Scrap leather is treated to recover fats therefrom and either for the production of a so-called "leather solution" for filling purposes &c. or for the production of a brown or yellow dye, by digesting the scrap leather with an alkali in an autoclave with steam under pressure, removing the solution obtained and treating it, after separation of liberated fats, with an acid, particularly nitric acid, either (a) for a period of 1 or more hours to obtain after neutralising a "leather solution," or (b) filtering off the solids obtained, followed by washing, neutralising and vacuum drying the solids to obtain a brown dye, or (c) treating the "leather solution" obtained as in (a) with further acid, particularly nitric acid, and proceeding as in (b) to obtain a yellow dye, fats being also separated off during or after the acid treatment. In the first stage treatment with alkali, a proportion of water is mixed with the leather scraps, the alkali is either caustic soda or caustic potash, and the temperature, depending on the steam pressure varies from 250 DEG to 360 DEG F. The treatment is continued with agitation until a neutral or slightly alkaline solution, which is soluble in water, is obtained. In the second stage treatment with acid according to the process (a) above, the solution obtained is fed into glass or enamelled containers equipped with stirring apparatus, allowed to cool to segregate fats which are removed, and then treated with the acid whilst stirring for the period specified, the vapours developed being exhausted from the containers. On completion the mass cools, more fat is segregated and is removed, and the solution is then neutralised and filtered to obtain the so-called "leather solution" which is capable of producing a hard filling for leather when dried. In the second stage treatment with acid according to the process (b) above, the solution obtained from the autoclave is filtered and then treated with the acid, which in this case may be H2SO4, when the solids are precipitated which are removed, washed, and dissolved in caustic soda or caustic potash. This solution is then vacuum dried and the solids obtained pulverized to form a brown dye. Preliminary p to the first stage of the processes, the scrap leather may be treated in the autoclave with water only and steam under pressure. On cooling, the surface layer of fats may be removed, and the undissolved scrap leather treated as in the main process.
100 FR993153D 1949-06-08 FR993153A 1951-10-29