会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 171. 发明授权
    • Starch adhesives and their preparation
    • 淀粉粘合剂及其制备
    • US3524750A
    • 1970-08-18
    • US3524750D
    • 1969-04-25
    • OGILVIE FLOUR MILLS CO LTD
    • BILLY JEAN-MARC
    • C08B31/00C09J103/02D21H17/28D21H19/54C09J3/06
    • D21H19/54C08B31/00C08L2666/02C09J103/02D21H17/28
    • 1302943 Starch adhesives OGILVIE FLOUR MILLS CO 22 April 1970 [25 April 1969] 19258/70 Heading C3U An adhesive composition, particularly suitable for use in the manufacture of laminated and corrugated paperboard, is made by preparing an aqueous caustic solution, e.g., from sodium hydroxide flakes, rapidly adding granular starch (corn, wheat or tapioca) to the solution in an amount such that the resulting slurry contains between 15% and 30% solids by weight, raising the temperature of the slurry, whereupon the starch granules swell, thickening the slurry, preferably permitting the swelling to continue until a Zahn #3 viscosity (defined) of 12 to 60 seconds is attained, and with the individual starch granules only partially gelatinized adding between 2 and 15% by weight, based on the initial starch weight, of a phenolic compound (resorcinol, phenol, phloroglucinol or pyrocatechol) as a reaction stopper (optionally with borax or alum) and finishing the adhesive by adding simultaneously with, or subsequently to, the phenolic compound an aldehyde (formaldehyde, furfural, glyoxal or acetaldehyde) in an amount such that the molar ratio of aldehyde to phenol is greater than 1 to 1 (up to 2À1:1). The temperature of the slurry may be slowly raised by direct steam injection until it is within the range 103-105‹ F. The partially gelatinized starch granules, phenol and aldehyde are stated to form a co-condensation resin. The compositions typically exhibit a pH of between 9 and 12, a gel temperature of between 131‹ and 161‹ F. and a viscosity of between 12 and 60 Zahn #3 seconds. They may additionally include a small proportion of a phenol-formaldehyde, urea-formaldehyde or acetone-formaldehyde resin.
    • 172. 发明授权
    • Method for manufacturing corrugated board
    • 制造腐蚀板的方法
    • US3434901A
    • 1969-03-25
    • US3434901D
    • 1965-10-23
    • WEST VIRGINIA PULP & PAPER CO
    • GRIFFITHS DARRELL J LMILLER KENYON WNIKKEL WILLEM A
    • B31F1/28C09J103/02B31F1/22C09J3/06
    • B31F1/2804C08L2666/02C09J103/02Y10T156/1025
    • 1,168,823. Paper laminate. WEST VIRGINIA PULP & PAPER CO. 19 Oct., 1966 [23 Oct., 1965], No. 46833/66. Heading B5N. In a method of bonding two paper or paperlike laminµ, a coating of raw starch in a liquid carrier is applied to the surface of one of the laminµ, the starch is brought to gel condition, the second lamina is then applied to the coating, and the laminate is consolidated by pressure. As described the raw starch is gelled by heat and/or by chemical additives which reduce its gel point. The raw starch may be raw corn, tapioca, or potato starch and the liquid carrier may consist of polyvinyl alcohol or of water and smaller amounts of cooked starch, borax and caustic soda, the raw starch comprising 10- 40% by weight of the adhesive. In making double-faced corrugated board by the method, single-faced board 1 is fed via a preheater 16 and an adhesive applicator 18 into contact with a liner 5 between belts 20 and rollers 23 constituting a compression section 19. The adhesive is gelled by spraying the coated board 1 with steam from pipes 24. If the heat applied by the preheater 16 is sufficient to gel the adhesive the pipes 24 may be omitted. In an alternative embodiment the adhesive is gelled by spraying with a gel point depressing additive e.g. caustic soda. The belts 20 may be replaced by a series of opposed rollers or air chambers. In a further embodiment further single-faced boards are combined with the board 1 and liner 5. In alternative embodiments two plane laminµ are combined between pressure rolls, adhesive being applied previously to one of the laminµ and gelled, or a plane lamina is passed between corrugating rolls and combined with a plane lamina to which the adhesive has been applied in stripes before gelling, to align with the tips of the corrugations in the corrugated lamina. Alternatively the adhesive is applied direct to the corrugation tips.
    • 176. 发明授权
    • Process for the manufacture of coldwater dispersible adhesives
    • 制造冷水可分散粘合剂的方法
    • US3284221A
    • 1966-11-08
    • US27493163
    • 1963-04-23
    • STALEY MFG CO A E
    • HUEBSCHMANN JOHN WWRIGHTSMAN JOHN H
    • C08B31/18C09J103/02
    • C09J103/02C08B31/18C08L2666/02C08L2666/28C08L2666/54
    • A dry, cold-water soluble amylaceous adhesive is made by acid hydrolysing, in presence of 0.1 to 3% by weight of terpineol, based on the weight of starch dry substance, an aqueous dispersion of a starch mixture containing not less than 5% by weight, on a dry solids basis, of an oxidized starch, to obtain a hydrolysed product having a Brookfield viscosity at 85 DEG F. and 20 r.p.m. of 50 to 20,000 c.p.s. measured in water at a solids content of 26%, adding to the hydrolysed product 7 to 25% by weight of borax based on the weight of the starch dry substance, cooling the resulting mixture from the hydrolysing temperature to less than 150 DEG F., adjusting the pH to 8.5 to 9.8 by adding an alkali metal hydroxide or alkaline earth metal hydroxide, and drying the resulting composition. The starch may be derived from e.g. corn, potato, waxy corn, tapioca or arrowroot. The mixture preferably contains 10-15% of oxidized starch, the remainder being raw or modified starches. The hydrolysis may be carried out at, e.g., 200-270 DEG F., under pressure. Specified acid catalysts are hydrochloric, sulphuric, acetic and phosphoric acids. The solids content of the starch dispersion is preferably 25 to 30%. The borax, which prevents further hydrolysis, may be added immediately to the hot hydrolysed product or after hydrolysis has been slowed by cooling. The composition may be dried by, e.g., spray- or roll-drying, and is then preferably ground. The composition may contain bleaches, e.g. sodium bisulphite and hydrogen peroxide, preservatives, e.g. copper sulphate, formaldehyde, zinc sulphate, and the sodium salts of ophenylphenol and pentachlorophenol, and defoaming agents, e.g. tributyl phosphate, tributyl citrate, heptanol, oleic acid and stearic acid.ALSO:A dry, cold-water soluble amylaceous adhesive is made by acid hydrolysing, in presence of 0.1 to 3% by weight of terpineol, based on the weight of starch dry substance, an aqueous dispersion of a starch mixture containing not less than 5% by weight, on a dry solids basis, of an oxidized starch, to obtain a hydrolysed product having a Brookfield viscosity at 85 DEG F. and 20 r.p.m. of 50 to 20,000 c.p.s. measured in water at a solids content of 26%, adding to the hydrolysed product 7 to 25% by weight of borax based on the weight of the starch, dry substance, cooling the resulting mixture from the hydrolysing temperature to less than 150 F., adjusting the pH to 8.5 to 9.8 by adding an alkali metal hydroxide or alkaline earth metal hydroxide, and drying the resulting composition. The starch may be derived from, e.g. corn, potato, waxy corn, tapioca or arrowroot. The mixture preferably contains 10-15% of oxidized starch, the remainder being raw or modified starches. The hydrolysis may be carried out at e.g. 200 DEG -270 DEG F., under pressure. Specified acid catalysts are hydrochloric, sulphuric, acetic and phosphoric acids. The solids content of the starch dispersion is preferably 25 to 30%. The borax, which prevents further hydrolysis, may be added immediately to the hot hydrolysed product or after hydrolysis has been slowed by cooling. The composition may be dried by, e.g spray- or roll-drying, and is then preferably ground. The composition may contain bleaches, e.g. sodium bisulphite and hydrogen peroxide, preservatives, e.g. copper sulphate, formaldehyde, zinc sulphate, and the sodium salts of o-phenylphenol and pentachlorophenol, and defoaming agents, e.g. tributyl phosphate, tributyl citrate, heptanol, oleic acid and stearic acid.
    • 177. 发明授权
    • Starch composition
    • US3234037A
    • 1966-02-08
    • US14128861
    • 1961-09-28
    • CORN PRODUCTS CO
    • SATTERTHWAITE ROBERT W
    • C04B24/38C04B28/14C09J103/02
    • C04B28/14C04B24/383C08L2666/02C08L2666/28C09J103/02C04B24/08
    • A tile-forming composition comprises water, gypsum, boric acid, paraffin wax, mineral wool and a starch composition comprising a thick boiling starch having a Scott viscosity at 200 DEG F. of 70 seconds based on 12 grams of dry starch or a super thick boiling starch having a Scott viscosity at 200 DEG F. of at least 60 seconds based on 11 grams of dry starch and a non-ionized polyhydric alcohol fatty acid ester. The starch may be corn, potato or tapioca starch. The esters specified are the laurate, stearate and palmitate esters of diethylene glycol, polyoxyethylene glycol monostearate, glycerol monostearate and sorbitan monostearate.ALSO:A starch binder composition which is suitable for addition to tile mixes, comprises a thick boiling starch having a Scott viscosity at 200 DEG F. of 70 seconds based on 12 grams of dry starch or a super thick boiling starch having a Scott viscosity at 200 DEG F. of at least 60 seconds based on 11 grams of dry starch at 200 DEG F. and a non-ionised polyhydric alcohol fatty acid ester. The starch may be corn, potato or tapioca starch. The esters specified are the laurate, stearate and palmitate esters of diethylene glycol, polyoxyethylene glycol monostearate, glycerol monostearate and sorbitan monostearate. The composition may be added to a tile mix comprising water, gypsum, boric acid, parafin wax and mineral wool.
    • 178. 发明授权
    • Polymers and their production
    • 聚合物及其生产
    • US3189578A
    • 1965-06-15
    • US80831059
    • 1959-04-23
    • DEERING MILLIKEN RES CORP
    • KUEMMERER HENRY R
    • C08F251/00C08G18/10C08G18/48C08G18/84C08L3/02C08L71/02C09J103/02C09J133/08D06M15/11D06M15/267D06M15/564
    • D06M15/564C08F251/00C08G18/10C08G18/4833C08G18/84C08L3/02C08L71/02C08L2666/02C09J103/02C09J133/08D06M15/11D06M15/267Y10S8/04Y10S8/18Y10T428/2933Y10T442/3049Y10T442/3228C08F220/12C08G18/2805C08G18/2815C08G18/302
    • A sizing composition comprises either: (i) the product obtained by polymerizing a C2-C4 alkyl acrylate with a gelatinized starch in the presence of a free-radical catalyst; or (ii) a blend of an aqueous starch paste and an aqueous emulsion of a polymerized C2-C4 alkyl acrylate, the compositions in both cases containing a nonionic surface active agent in an amount up to 30% of the combined weight of starch and acrylic ester, the water-soluble portion of the agent being a polyoxyethylene of from 2 to 120 units, and the ratio of starch to acrylic ester lying in the range of 7:3 to 1:19. The polymerized acrylic ester may contain a comonomer such as acrylic, methacrylic or itaconic acid, maleic anhydride or acrylamide. The starch used may be a native starch or a modified starch, e.g. oxidized, acid-modified or etherified, or a dextrin. The free-radical catalyst may be hydrogen peroxide, benzoyl peroxide, t-butyl hydroperoxide, sodium hypochlorite, persulphates and redox systems. Preferred surface active agents are octylphenoxy, nonylphenoxy, dioctylphenoxy, tridecylphenoxy and lauryl ethers of polyoxyethylenes.ALSO:Hydrophobic fibres, e.g. polyester fibres, are sized by applying thereto a composition comprising either: (i) the product obtained by polymerizing a C2-C4 alkyl acrylate with a gelatinized starch in the presence of a freeradical catalyst; or (ii) a blend of an aqueous starch paste and an aqueous emulsion of a polymerized C2-C4 alkyl acrylate, the compositions in both cases containing a non-ionic surface active agent in an amount up to 30% of the combined weight of acrylic ester and starch, the water-soluble portion of the agent being a polyoxyethylene of from 2 to 120 units, and the ratio of starch to acrylic ester lying within the range of 7:3 to 1:19. The polymerized acrylic ester may contain a comonomer, e.g. acrylic, methacrylic or itaconic acid, maleic acrylic, aretharacrific or itaconic acid, maleic anhydride or acrylamide. The starch may be a native starch or a modified starch, e.g. oxidized, acid-modified or etherified, or a dextrin. Preferred surface active agents are octylphenoxy, dioctylphenoxy, nonylphenoxy, tridecylphenoxy and lauryl ethers of polyoxyethylenes.
    • 180. 发明授权
    • Sizing textile yarns
    • 调整纺织纱线
    • US3061470A
    • 1962-10-30
    • US80829759
    • 1959-04-23
    • DEERING MILLIKEN RES CORP
    • KUEMMERER HENRY R
    • C08F251/00C08G18/10C08G18/48C08G18/84C08L3/02C08L71/02C09J103/02C09J133/08D06M15/11D06M15/267D06M15/564
    • D06M15/564C08F251/00C08G18/10C08G18/4833C08G18/84C08L3/02C08L71/02C08L2666/02C09J103/02C09J133/08D06M15/11D06M15/267Y10S8/04Y10S8/18Y10T428/2933Y10T442/3049Y10T442/3228C08F220/12C08G18/2805C08G18/2815C08G18/302
    • A sizing composition comprises either: (i) the product obtained by polymerizing a C2-C4 alkyl acrylate with a gelatinized starch in the presence of a free-radical catalyst; or (ii) a blend of an aqueous starch paste and an aqueous emulsion of a polymerized C2-C4 alkyl acrylate, the compositions in both cases containing a nonionic surface active agent in an amount up to 30% of the combined weight of starch and acrylic ester, the water-soluble portion of the agent being a polyoxyethylene of from 2 to 120 units, and the ratio of starch to acrylic ester lying in the range of 7:3 to 1:19. The polymerized acrylic ester may contain a comonomer such as acrylic, methacrylic or itaconic acid, maleic anhydride or acrylamide. The starch used may be a native starch or a modified starch, e.g. oxidized, acid-modified or etherified, or a dextrin. The free-radical catalyst may be hydrogen peroxide, benzoyl peroxide, t-butyl hydroperoxide, sodium hypochlorite, persulphates and redox systems. Preferred surface active agents are octylphenoxy, nonylphenoxy, dioctylphenoxy, tridecylphenoxy and lauryl ethers of polyoxyethylenes.ALSO:Hydrophobic fibres, e.g. polyester fibres, are sized by applying thereto a composition comprising either: (i) the product obtained by polymerizing a C2-C4 alkyl acrylate with a gelatinized starch in the presence of a freeradical catalyst; or (ii) a blend of an aqueous starch paste and an aqueous emulsion of a polymerized C2-C4 alkyl acrylate, the compositions in both cases containing a non-ionic surface active agent in an amount up to 30% of the combined weight of acrylic ester and starch, the water-soluble portion of the agent being a polyoxyethylene of from 2 to 120 units, and the ratio of starch to acrylic ester lying within the range of 7:3 to 1:19. The polymerized acrylic ester may contain a comonomer, e.g. acrylic, methacrylic or itaconic acid, maleic acrylic, aretharacrific or itaconic acid, maleic anhydride or acrylamide. The starch may be a native starch or a modified starch, e.g. oxidized, acid-modified or etherified, or a dextrin. Preferred surface active agents are octylphenoxy, dioctylphenoxy, nonylphenoxy, tridecylphenoxy and lauryl ethers of polyoxyethylenes.