| 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 | Functionalized polymer compositions | US15047669 | 2016-02-19 | US09410036B2 | 2016-08-09 | Graciela B. Arhancet; Matthew Mahoney; Xiaojun Wang; Rangarani Karnati |
| The invention relates to functionalized polymers including homopolymers and copolymers and their uses in industrial applications and in agricultural applications. In particular, the homopolymers and copolymers may be, for example, used in polymer blends, used as nutritives and in feed compositions, and used in combination with a pharmaceutical or nutritive. | ||||||
| 22 | FUNCTIONALIZED POLYMER COMPOSITIONS | US15047669 | 2016-02-19 | US20160185899A1 | 2016-06-30 | Graciela B. Arhancet; Matthew Mahoney; Xiaojun Wang; Rangarani Karnati |
| The invention relates to functionalized polymers including homopolymers and copolymers and their uses in industrial applications and in agricultural applications. In particular, the homopolymers and copolymers may be, for example, used in polymer blends, used as nutritives and in feed compositions, and used in combination with a pharmaceutical or nutritive. | ||||||
| 23 | POLYMERS, SUBSTRATES, METHODS FOR MAKING SUCH, AND DEVICES COMPRISING THE SAME | US14765971 | 2014-02-06 | US20150368411A1 | 2015-12-24 | Nicholas Brendan Duck |
| The present invention relates generally to substrates for making polymers and methods for making polymers. The present invention also relates generally to polymers and devices comprising the same. | ||||||
| 24 | Polymers, substrates, methods for making such, and devices comprising the same | US14173452 | 2014-02-05 | US09200106B2 | 2015-12-01 | Nicholas Brendan Duck |
| The present invention relates generally to substrates for making polymers and methods for making polymers. The present invention also relates generally to polymers and devices comprising the same. | ||||||
| 25 | CROSS-LINKED POLYCARBONATE RESIN WITH IMPROVED CHEMICAL AND FLAME RESISTANCE | US14701620 | 2015-05-01 | US20150315336A1 | 2015-11-05 | Jean-Francois Morizur; Paul Dean Sybert; James Franklin Hoover; Derek Lake |
| Disclosed herein are compositions including a cross-linked polycarbonate. The cross-linked polycarbonate may be derived from a polycarbonate having about 0.5 mol % to about 5 mol % endcap groups derived from a monohydroxybenzophenone. A plaque including the composition can achieve a UL94 5VA rating. Also disclosed herein are articles including the compositions, methods of using the compositions, and processes for preparing the compositions. | ||||||
| 26 | PROCESSES FOR ENHANCING FLAME RETARDANCE AND CHEMICAL RESISTANCE OF POLYMERS | US14607444 | 2015-01-28 | US20150218309A1 | 2015-08-06 | Jean-Francois Morizur; Paul Dean Sybert; Amanda Marie Flores; Peter Johnson; Andrew Frazee; Thomas L. Evans |
| Processes for increasing the chemical resistance of a surface of a formed article are disclosed. The formed article is produced from a polymeric composition comprising a photoactive additive containing photoactive groups derived from a monofunctional benzophenone. The surface of the formed article is then exposed to ultraviolet light to cause crosslinking of the photoactive additive and produce a crosslinked surface. The crosslinking enhances the chemical resistance of the surface. Various means for controlling the depth of the crosslinking are also discussed. | ||||||
| 27 | CROSS-LINKED POLYCARBONATE RESIN WITH IMPROVED CHEMICAL AND FLAME RESISTANCE | US14560354 | 2014-12-04 | US20150197609A1 | 2015-07-16 | Jean-Francois Morizur; Paul Dean Sybert |
| Disclosed herein are compositions including a cross-linked polycarbonate. The cross-linked polycarbonate may be derived from a polycarbonate having about 0.5 mol % to about 5 mol % endcap groups derived from a monohydroxybenzophenone. A plaque including the composition can achieve a UL94 5VA rating. Also disclosed herein are articles including the compositions, methods of using the compositions, and processes for preparing the compositions. | ||||||
| 28 | PROCESSES FOR ENHANCING FLAME RETARDANCE AND CHEMICAL RESISTANCE OF POLYMERS | US14607399 | 2015-01-28 | US20150147557A1 | 2015-05-28 | Jean-Francois Morizur; Paul Dean Sybert; Amanda Marie Flores; Peter Johnson; Andrew Frazee; Thomas L. Evans |
| Processes for increasing the chemical resistance of a surface of a formed article are disclosed. The formed article is produced from a polymeric composition comprising a photoactive additive containing photoactive groups derived from a monofunctional benzophenone. The surface of the formed article is then exposed to ultraviolet light to cause crosslinking of the photoactive additive and produce a crosslinked surface. The crosslinking enhances the chemical resistance of the surface. Various means for controlling the depth of the crosslinking are also discussed. | ||||||
| 29 | Cross-linked polycarbonate resin with improved chemical and flame resistance | US14137121 | 2013-12-20 | US09023973B2 | 2015-05-05 | Jean-Francois Morizur; Paul Dean Sybert; James Franklin Hoover; Derek Lake |
| Disclosed herein are compositions including a cross-linked polycarbonate. The cross-linked polycarbonate may be derived from a polycarbonate having about 0.5 mol % to about 5 mol % endcap groups derived from a monohydroxybenzophenone. A plaque including the composition can achieve a UL94 5VA rating. Also disclosed herein are articles including the compositions, methods of using the compositions, and processes for preparing the compositions. | ||||||
| 30 | CYANATE RESIN BLENDS AND RADOMES INCLUDING THEM | US14314059 | 2014-06-25 | US20150002364A1 | 2015-01-01 | Kapsoo Cheon; Marie J. Hersman; Ajay Padwal |
| Certain embodiments are directed to cyanate resin blends comprising, for example, a mixture of a cyanate monomer and a cyanate oligomer. The resin blends are effective to provide a dielectric constant of less than 2.7, a glass transition temperature of at least 150° C. and a moisture absorption of less than 1.5%. Radomes using the resin are also described. | ||||||
| 31 | POLYMERS, SUBSTRATES, METHODS FOR MAKING SUCH, AND DEVICES COMPRISING THE SAME | US14173269 | 2014-02-05 | US20140220457A1 | 2014-08-07 | Nicholas Brendan Duck |
| The present invention relates generally to substrates for making polymers and methods for making polymers. The present invention also relates generally to polymers and devices comprising the same. | ||||||
| 32 | CROSS-LINKED POLYCARBONATE RESIN WITH IMPROVED CHEMICAL AND FLAME RESISTANCE | US14137002 | 2013-12-20 | US20140179844A1 | 2014-06-26 | Jean-Francois Morizur; Paul Dean Sybert |
| Disclosed herein are compositions including a cross-linked polycarbonate. The cross-linked polycarbonate may be derived from a polycarbonate having about 0.5 mol % to about 5 mol % endcap groups derived from a monohydroxybenzophenone. A plaque including the composition can achieve a UL94 5VA rating. Also disclosed herein are articles including the compositions, methods of using the compositions, and processes for preparing the compositions. | ||||||
| 33 | Preparation of aromatic oligomers | US296907 | 1989-01-11 | US4879366A | 1989-11-07 | Viktors Jansons; Heinrich C. Gors |
| Aromatic oligomers, in particular arylene ketone and arylene sulfone oligomers, are prepared by reacting an appropriate monomer system in the presence of free Lewis acid and a complex between a Lewis acid, for example, aluminum trichloride, and a Lewis base, for example, N,N-dimethylformamide, and, optionally, a diluent, such as methylene chloride. The process is particularly advantageous for the preparation of substantially or all paralinked arylene ether ketone oligomers as the presence of the Lewis acid/Lewis base complex markedly reduces alkylation and ensures the substantial absence of ortho substitution. The monomer system can be, for example, a self-reacting monomer such as p-phenoxy-benzoyl chloride or a two-monomer system such as 1,4-diphenoxybenzene and terephthaloyl chloride. | ||||||
| 34 | Drug delivery devices manufactured from poly(orthoesters) and poly(orthocarbonates) | US544808 | 1975-01-28 | US4093709A | 1978-06-06 | Nam Sok Choi; Jorge Heller |
| The invention concerns orthoester and orthocarbonate polymers having a repeating mer comprising a hydrocarbon radical and a symmetrical dioxycarbon unit of the general formula: ##STR1## WHEREIN R.sub.1 is a multivalent hydrocarbon radical, R.sub.2 and R.sub.3 are hydrocarbon radicals with at least one of R.sub.2 or R.sub.3 bonded to the dioxycarbon through an oxygen linkage, and which polymers are synthesized by reacting a polyol with an orthoester or orthocarbonate. The polymers are useful for making articles of manufacture, including devices and coatings for delivering beneficial agents. | ||||||
| 35 | Photopolymerized polycarboxylic acid anhydride film coating and product,and method of forming | US3713874D | 1970-12-15 | US3713874A | 1973-01-30 | WRIGHT A; MATHEWSON W |
| A THIN, CONTINUOUS FILM IS FORMED ON A SUBSTRATE BY ULTRAVIOLET SURFACE PHOTOPOLYMERIZATION OF A MATERIAL IN THE GASEOUS PHASE. THE MATERIAL IS SELECTED FROM VARIOUS ANHYDRIDES AND DIANHYDRIDES. SUCH FILMS, WHICH CAN BE SELECTIVELY FORMED AS ELECTRICALLY INSULATING OR ELECTRICALLY CONDUCTIVE, ARE USEFUL AS COATINGS ON METALLIC AND NONMETALLIC SUBSTRATES, AND FOR CORROSION PROTECTION. THE ELECTRICALLY INSULATING FILMS ARE USEFUL FURTHER AS CAPACITOR DIELECTRICS, CRYOGENIC DEVICE INSULATION, INSULATION FOR MICROELECTRIC DEVICES, AND PRIMER OR INSULTION ON ELECTRICALLY CONDUCTIVE WIRE, WHILE THE ELECTRICALLY CONDUCTIVE FILMS CAN ALSO BE EMPLOYED AS CONDUCTIVE LAYERS IN MICROELECTRIC DEVICES.
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| 36 | Fluorinated oxygen-containing products and process for preparation thereof | US3699145D | 1970-05-01 | US3699145A | 1972-10-17 | SIANESI DARIO; PASETTI ADOLFO; CORTI COSTANTE |
| Perfluorinated cyclic ethers and fluorinated linear polyethers. Prepared by photochemical reaction in liquid phase of perfluoropropylene with oxygen in presence of ultraviolet radiation.
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| 37 | Process for preparing fluorinated oxygen-containing copolymers | US3650928D | 1969-04-02 | US3650928A | 1972-03-21 | SIANESI DARIO; PASETTI ADOLFO; CORTI COSTANTE |
| PERFLUORINATED LINEAR POLYETHERS ARE PREPARED BY LIQUID PHASE PHOTOCHEMICAL REACTION OF A MIXTURE OF PERFLUOROPROPYLENE AND TETRAFLUOROETHYLENE WITH OXYGEN IN THE PRESENCE OF ULTRAVIOLET RADIATION.
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| 38 | Photopolymerized film, composite thereof, and method of forming | US3619259D | 1969-04-01 | US3619259A | 1971-11-09 | WRIGHT ARCHIBALD N; MATHEWSON WILFRED F JR |
| A thin, continuous film is formed on a substrate by the ultraviolet surface polymerization of the vapor of an imide containing photopolymerizable organic material. Such films are useful as coatings on metallic and nonmetallic substrates, capacitor dielectrics, cryogenic device insulation, insulation for microelectric devices, insulation on electrically conductive wire, and for corrosion protection.
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| 39 | Diamond and boron nitride particles coated with a polymerized dianhydride | US3578425D | 1967-03-14 | US3578425A | 1971-05-11 | WRIGHT ARCHIBALD N; MATHEWSON WILFRED F JR |
| A THIN, CONTINUOUS FILM IS FORMED ON A SUBSTRATE BY ULTRAVIOLET SURFACE PHOTOPOLYMERIZATION OF A MATERIAL IN THE GASEOUS PHASE. THE MATERIAL IS SELECTED FROM VARIOUS ANHYDRIDES AND DIANHYDRIDES. SUCH FILMS, WHICH CAN BE SELECTIVELY FORMED AS ELECTRICALLY INSULATING OR ELECTRICALLY CONDUCTIVE, ARE USEFUL AS COATINGS ON METALIC AND NONMETALLIC SUBSTRATES, AND FOR CORROSION PROTECTION. THE ELECTRICALLY INSULATING FILMS ARE USEFUL FURTHER AS CAPACITOR DIELECTRICS, CRYOGENIC DEVICE INSULATION, INSULATION FOR MICROELECTRIC DEVICES, AND PRIMER OR INSULATION ON ELECTRI-
CALLY CONDUCTIVE WIRE, WHILE THE ELECTRICALLY CONDUCTIVE FILMS CAN ALSO BE EMPLOYED AS CONDUCTIVE LAYERS IN MICROELECTRIC DEVICES. |
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| 40 | Polyamides containing the divalent 9,10-triptycene radical | US3542734D | 1967-03-17 | US3542734A | 1970-11-24 | RIPPIE WALLACE LARIMER |
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