序号 | 专利名 | 申请号 | 申请日 | 公开(公告)号 | 公开(公告)日 | 发明人 |
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61 | of munich | US1625852D | US1625852A | 1927-04-26 | ||
62 | Process of resinifying aliphatic aldehydes | US59497322 | 1922-10-16 | US1600113A | 1926-09-14 | HERRMANN WILLY O; HANS DEUTSCH |
63 | Refining aldehyde resins | US56362822 | 1922-06-15 | US1596971A | 1926-08-24 | HERRMANN WILLY O; HANS DEUTSCH |
64 | Polymerization of butyraldehyde | US71773624 | 1924-06-04 | US1576503A | 1926-03-16 | CHARLES BOGIN |
65 | Keto-alcohol resin and process of making the same | US53976322 | 1922-02-27 | US1557571A | 1925-10-20 | CARLETON ELLIS |
66 | OIL-BASED INK COMPOSITION FOR WRITING INSTRUMENT, AND WRITING INSTRUMENT, MARKING PEN, AND BALLPOINT PEN CONTAINING SAME | EP16800038.8 | 2016-05-25 | EP3305861A1 | 2018-04-11 | NAKAMURA Hisashi |
[Problem] Provided is an oil-based ink composition for a writing instrument, which can form handwriting having excellent water resistance in which no bleeding occurs on written surfaces of various materials with a dye retaining color development. [Solution] An oil-based ink composition for a writing instrument, comprising a dye, an organic solvent and a phenolic compound of the following general formula (1):
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67 | RESINS | EP10790468.2 | 2010-12-10 | EP2510025A1 | 2012-10-17 | FITCHETT, Colin, Stanley; CHAPPELL, Colin, Graham |
The present invention relates to methods for the production of a resin such as a thermosetting resin, particularly a bioresin, components for use in the methods, and products obtained from the methods. In one aspect the method of forming a resin comprising the steps of: (1 ) providing an aldehyde-cross-linking agent condensate obtained by reacting a volatile aldehyde with a cross-linking agent; (2) providing a non-volatile aldehyde; and (3) combining the aldehyde- cross-linking agent condensate and the non-volatile aldehyde, thereby forming the resin. | ||||||
68 | PHOTO-RESPONSIVE MICROENCAPSULATION MATERIALS, COMPOSITIONS AND METHODS OF USE THEREOF | EP06839611.8 | 2006-10-30 | EP1945344A2 | 2008-07-23 | STOWELL, Michael, H., B. |
Photoactivatable prepolymers and methods of use thereof are disclosed for microencapsulation of a substantially water-insoluble material within a nonporous shell. As provided herein, the microencapsulated material is released with no more than a slow release rate. Upon exposure of the nonporous shell to light, the nonporous shell is converted into a porous shell having an increased release rate for the microencapsulated material. | ||||||
69 | MANUFACTURE OF POLYKETONES | EP00910380.5 | 2000-03-01 | EP1165649A1 | 2002-01-02 | GOLDFINGER, Marc, Bruce |
Polyketones are manufactured by reacting an aromatic carboxylic acid with a bireactive aromatic compound, using as a catalyst a combination of a carboxylic acid anhydride and phosphoric acid, or equivalents thereof. The product polymers are useful as molding resins. | ||||||
70 | Acrolein freisetzende Copolymere | EP97101161.4 | 1997-01-25 | EP0792895B1 | 2001-05-16 | Werle, Peter, Dr.; Trageser, Martin; Krimmer, Hans-Peter, Dr.; Kunz, Franz-Rudolf |
71 | Acrolein freisetzende Copolymere | EP97101161.4 | 1997-01-25 | EP0792895A1 | 1997-09-03 | Werle, Peter, Dr.; Trageser, Martin; Krimmer, Hans-Peter, Dr.; Kunz, Franz-Rudolf |
Acroleinpolymer, hergestellt aus Acrolein und einem oder mehreren mehrwertigen Alkoholen, gekennzeichnet durch |
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72 | Aus Polyaldehyden aufgebaute gasenthaltende Mikropartikel als Kontrastmittel | EP91250038.6 | 1991-02-11 | EP0441468B1 | 1996-09-11 | Rössling, Georg, Dr.; Albayrak, Celal, Dr.; Rothe, Matthias, Dr.; Siegert, Joachim, Dr. |
73 | Novel initiators for cationic polymerization | EP91300764.7 | 1991-01-31 | EP0442635A1 | 1991-08-21 | Farooq, Omar, c/o Minnesota Mining and |
Disclosed are novel compounds which are useful as initiators for cationically polymerizable monomers. The novel compounds comprise a carbon containing cation (e.g., trimethyloxonium) which is capable of initiating cationic polymerization and a non-nucleophilic counterion which is an at least partially fluorinated hydrocarbylsulfonato metallate (e.g. perfluoroethylsulfonato-aluminate). The disclosed initiators are capable of initiating the cationic polymerization of a wide variety of monomers such as epoxides, tetrahydrofuans, oxazolines, vinyls, lactones, and the like. |
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74 | Aus Polyaldehyden aufgebaute gasenthaltende Mikropartikel als Kontrastmittel | EP91250038.6 | 1991-02-11 | EP0441468A2 | 1991-08-14 | Rössling, Georg, Dr.; Albayrak, Celal, Dr.; Rothe, Matthias, Dr.; Siegert, Joachim, Dr. |
Mikropartikel bestehend aus bioabbaubaren Polymeren, |
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75 | Verwendung von Polykondensationsprodukten aus Acrolein und Formaldehyd als Biozide | EP82110923.8 | 1982-11-26 | EP0087509A1 | 1983-09-07 | Merk, Wolfgang, Dr. Dipl.-Chem.; Rink, Karl-Heinz, Dr. Dipl.-Chem. |
Als Biozide für wäßrige Systeme werden wasserlösliche niedermolekulare Polykondensationsprodukte eingesetzt, die durch Kondensation von Acrolein und Formaldehyd im molaren Verhältnis zwischen 1:1 und 1:10 in wäßrigem oder wäßrig-organischem Medium in Gegenwart eines basischen Katalysators hergestellt wurden. Die Kondensationsreaktion kann auch in zusätzlicher Gegenwart von wasserlöslichen ein- oder mehrwertigen Alkoholen und/oder Säureamiden vorgenommen werden. |
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76 | PHOTO-RESPONSIVE MICROENCAPSULATION MATERIALS, COMPOSITIONS AND METHODS OF USE THEREOF | PCT/US2006060351 | 2006-10-30 | WO2007051198A3 | 2007-07-26 | STOWELL MICHAEL H B |
Photoactivatable prepolymers and methods of use thereof are disclosed for microencapsulation of a substantially water-insoluble material within a nonporous shell. As provided herein, the microencapsulated material is released with no more than a slow release rate. Upon exposure of the nonporous shell to light, the nonporous shell is converted into a porous shell having an increased release rate for the microencapsulated material. | ||||||
77 | USE OF A POLY-KETONIC COSMETIC PACKAGING MATERIAL AND A DISPENSER SYSTEM FOR A PRESSURISED PRODUCT, CONTAINING AT LEAST ONE PART MADE OF, OR INCLUDING SAID POLY-KETONIC MATERIAL | US16000855 | 2018-06-05 | US20180346176A1 | 2018-12-06 | Mohamed ELMEGUENNI |
Embodiments of the invention include a poly-ketonic cosmetic package for fluid dispenser systems. | ||||||
78 | SELF-IMMOLATIVE POLYMERS, ARTICLES THEREOF, AND METHODS OF MAKING AND USING SAME | US15830864 | 2017-12-04 | US20180155483A1 | 2018-06-07 | Paul A. Kohl; Oluwadamilola Phillips; Jared Schwartz; Gerald Gourdin; Anthony Engler; Jisu Jiang |
Self-immolative polymers and compositions comprising such polymers are described. The polymers are copolymers of phthalaldehyde and one or more additional aldehydes and can degrade/decompose upon exposure to a desired stimulus, like light, heat, sound, or chemical trigger. The copolymers can be linear or cyclic, and can be crosslinked or uncrosslinked. Polymer compositions, including multilayered and multiregioned compositions, containing the copolymers are disclosed. These compositions can contain agents such as crosslinking agents, crosslinking catalysts, photocatalysts, theremocatalyts, sensitizers, chemical amplifiers, freezing point depressing agent, photo-response delaying agents, and the like. Methods of making and using the copolymers are also described. | ||||||
79 | Protein-polymer-drug conjugates | US14834159 | 2015-08-24 | US09770519B2 | 2017-09-26 | Aleksandr Yurkovetskiy; Mao Yin; Timothy B. Lowinger; Joshua D. Thomas; Charles E. Hammond; Cheri A. Stevenson; Natalya D. Bodyak; Patrick R. Conlon; Dmitry R. Gumerov |
A drug conjugate is provided herein. The conjugate comprises a protein based recognition-molecule (PBRM) and a polymeric carrier substituted with one or more -LD-D, the protein based recognition-molecule being connected to the polymeric carrier by LP. Each occurrence of D is independently a therapeutic agent having a molecular weight ≦5 kDa. LD and LP are linkers connecting the therapeutic agent and PBRM to the polymeric carrier respectively. Also disclosed are polymeric scaffolds useful for conjugating with a PBRM to form a polymer-drug-PBRM conjugate described herein, compositions comprising the conjugates, methods of their preparation, and methods of treating various disorders with the conjugates or their compositions. | ||||||
80 | Process for producing phenol | US14343199 | 2012-08-09 | US09388103B2 | 2016-07-12 | Kun Wang; Roberto Garcia; Francisco M. Benitez |
In a process for producing phenol, a feed comprising cyclohexylbenzene hydroperoxide is contacted with a cleavage catalyst comprising an acidic ionic liquid under cleavage conditions effective to cleave at least a portion of said cyclohexylbenzene hydroperoxide and produce a cleavage product stream comprising phenol and cyclohexanone. |