| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 61 | Composites transmissive to visual and infrared radiation and compositions and methods for making the composites | US14807872 | 2015-07-23 | US09670379B2 | 2017-06-06 | Andrew P. Nowak; April R. Rodriguez; Erin E. Stache |
| A composition comprises a copolymer made from a thiol terminated hydrocarbon monomer and at least one additional monomer chosen from the compounds of i) a terminally unsaturated hydrocarbon monomer, ii) an isocyanate functionalized hydrocarbon monomer and iii) a silane monomer substituted with two or more C2 to C8 terminally unsaturated alkenyl groups or C2 to C8 terminally unsaturated alkynyl groups. The composition also includes a particulate filler dispersed in the copolymer and a solvent. If the terminally unsaturated hydrocarbon monomer is polybutadiene, the polybutadiene contains from about 0 mol % to about 30 mol % of polymer units in a cis-1,4-butadiene form. Composites made from the composition and methods for making composite panels are also disclosed. | ||||||
| 62 | PHOTORESIST POLYMERS AND METHODS OF FORMING PATTERNS | US14804775 | 2015-07-21 | US20160159974A1 | 2016-06-09 | Jin PARK; Hyun-Woo KIM |
| A photoresist polymer is synthesized from a repeating unit that comprises a first leaving group including an ester group, and a second leaving group capable of being removed together with the first leaving group. | ||||||
| 63 | Controlled release fertilizers made from cross-linked glyceride mixtures | US13291681 | 2011-11-08 | US08790437B2 | 2014-07-29 | Romem Avdala; Leslie L. Carstens; Garrard Lee Hargrove; Sriramakrishna Maruvada; Baozhong Xing |
| A controlled release fertilizer material comprising a particulate plant nutrient surrounded by a coating which is the reaction product of a mixture including a cross-linked polyol, an isocyanate and a wax is described. The cross-linked polyol is a reaction product of a polyhydroxyl compound, such as glycerol, and a triglyceride and the monoglyceride and/or diglyceride products are cross-linked with sulfur, oxygen and/or a peroxide cross-linking moiety, or are directly cross-linked at unsaturated sites in the monoglycerides and/or diglycerides. | ||||||
| 64 | Adhesive tissue repair patch and collagen sheets | US12787304 | 2010-05-25 | US08617584B2 | 2013-12-31 | Louis C. Sehl; Olof Mikael Trollsas; Donald G. Wallace; David Toman; Frank A. DeLustro; Jacqueline A. Schroeder; George H. Chu |
| The present invention relates generally to synthetic polymer compositions that form interpenetrating polymer networks. In a preferred embodiment, the compositions comprise two multifunctionally activated synthetic polymers, along with a tensile strength enhancer. Such compositions form matrices that exhibit superior cohesive strength and in many instances can serve as adequate replacements for surgical means of attaching tissues, such as sutures, sponges and medical staples. | ||||||
| 65 | CONTROLLED RELEASE FERTILIZERS MADE FROM CROSS-LINKED GLYCERIDE MIXTURES | US13291681 | 2011-11-08 | US20120111076A1 | 2012-05-10 | ROMEM AVDALA; Leslie L. Carstens; Garrard Lee Hargrove; Sriramakrishna Maruvada; Baozhong Xing |
| A controlled release fertilizer material comprising a particulate plant nutrient surrounded by a coating which is the reaction product of a mixture including a cross-linked polyol, an isocyanate and a wax is described. The cross-linked polyol is a reaction product of a polyhydroxyl compound, such as glycerol, and a triglyceride and the monoglyceride and/or diglyceride products are cross-linked with sulfur, oxygen and/or a peroxide cross-linking moiety, or are directly cross-linked at unsaturated sites in the monoglycerides and/or diglycerides. | ||||||
| 66 | Thiol ester compositions and processes for making and using same | US11060675 | 2005-02-17 | US07989655B2 | 2011-08-02 | Mitchell D. Refvik; Daniel M. Hasenberg; Michael S. Hankinson; Michael S. Matson; Dale M. Solaas; Steven J. Herron; Jim D. Byers |
| Thiol ester compositions, methods of making the thiol ester compositions, and methods of using the thiol ester compositions are provided. In some embodiments, the thiol ester compositions include thiol esters, hydroxy thiol esters and cross-linked thiol esters. The thiol ester composition can be used to produce cross-linked thiol esters, sulfonic acid-containing esters, sulfonate containing esters and thioacrylate containing esters. The thiol ester compositions can be used to produce polythiourethanes. The polythiourethanes can be used in fertilizers and fertilizer coatings. | ||||||
| 67 | Thioester-ester-amide copolymers | US11821995 | 2007-06-25 | US07927621B2 | 2011-04-19 | Mikael O. Trollsas; Nam D. Pham; Michael H. Ngo; Bozena Zofia Maslanka |
| A poly(thioester ester amide) copolymer and method of making and using the same are disclosed. | ||||||
| 68 | Compositions and systems for forming crosslinked biomaterials and methods of preparation of use | US11344752 | 2006-01-31 | US07883693B2 | 2011-02-08 | Louis C. Sehl; Olof Mikael Trollsas; Donald G. Wallace; David Toman; Frank A. DeLustro; Jacqueline A. Schroeder; George H. Chu |
| Crosslinkable compositions are provided that readily crosslink in situ to provide biocompatible, nonimmunogenic crosslinked materials that may be used as adhesive compositions. The compositions comprise collagen and a plurality of crosslinkable components having reactive functional groups thereon, with the functional groups selected so as to enable inter-reaction between the components, i.e., crosslinking. Methods for preparing and using the compositions are also provided. Exemplary uses include tissue augmentation, biologically active agent delivery, bioadhesion, prevention of adhesions following surgery or injury, and coating of surgically acceptable patches and solid implants, the latter including sutures. | ||||||
| 69 | Controlled release fertilizer material and process for production thereof | US11059647 | 2005-02-17 | US07713326B2 | 2010-05-11 | Leslie E. Carstens; Baozhong Xing; Mitchell D. Refvik; Jim D. Byers |
| Thiol ester compositions, methods of making the thiol ester compositions, and methods of using the thiol ester compositions are provided. In some embodiments, the thiol ester compositions include thiol esters, hydroxy thiol esters and cross-linked thiol esters. The thiol ester composition can be used to produce cross-linked thiol esters, sulfonic acid-containing esters, sulfonate containing esters and thioacrylate containing esters. The thiol ester compositions can be used to produce polythiourethanes. The polythiourethanes can be used in fertilizers and fertilizer coatings. | ||||||
| 70 | Thiol ester compositions and processes for making and using same | US11060696 | 2005-02-17 | US07557236B2 | 2009-07-07 | Chad W. Brown; Mitchell D. Refvik; Steven J. Herron |
| Thiol ester compositions, methods of making the thiol ester compositions, and methods of using the thiol ester compositions are provided. In some embodiments, the thiol ester compositions include thiol esters, hydroxy thiol esters and cross-linked thiol esters. The thiol ester composition can be used to produce cross-linked thiol esters, sulfonic acid-containing esters, sulfonate containing esters and thioacrylate containing esters. The thiol ester compositions can be used to produce polythiourethanes. The polythiourethanes can be used in fertilizers and fertilizer coatings. | ||||||
| 71 | Thioester-ester-amide copolymers | US11821995 | 2007-06-25 | US20080319551A1 | 2008-12-25 | Mikael O. Trollsas; Nam D. Pham; Michael H. Ngo; Bozena Zofia Maslanka |
| A poly(thioester ester amide) copolymer and method of making and using the same are disclosed. | ||||||
| 72 | Polymers of aliphatic thioester | US11657433 | 2007-01-23 | US20080175882A1 | 2008-07-24 | Mikael O. Trollsas; Nam D. Pham; Michael H. Ngo |
| A coating comprising a polymer that comprises units derived from an aliphatic thioester on a medical device is provided. | ||||||
| 73 | POLYMER COMPOSITIONS AND PROCESSES FOR MAKING AND USING SAME | US11464318 | 2006-08-14 | US20070055033A1 | 2007-03-08 | Jim Byers; Mitchell Refvik; Chad Brown; Michael Matson |
| Poly(β-thioether ester) compositions, methods of making the poly(β-thioether ester) compositions, and methods of using the poly(β-thioether ester) compositions are provided. The poly(β-thioether ester) can be produced by contacting a thiol ester composition and an α,β-unsaturated ester to produce a mixture and then heating the mixture to produce the poly(β-thioether ester). In some embodiments, the thiol ester compositions include thiol esters, hydroxy thiol esters, and cross-linked thiol esters. | ||||||
| 74 | Thiol ester compositions and processes for making and using same | US11059792 | 2005-02-17 | US20050197390A1 | 2005-09-08 | Jim Byers; Mitchell Refvik; Chad Brown |
| Thiol ester compositions, methods of making the thiol ester compositions, and methods of using the thiol ester compositions are provided. In some embodiments, the thiol ester compositions include thiol esters, hydroxy thiol esters and cross-linked thiol esters. The thiol ester composition can be used to produce cross-linked thiol esters, sulfonic acid-containing esters, sulfonate containing esters and thioacrylate containing esters. The thiol ester compositions can be used to produce polythiourethanes. The polythiourethanes can be used in fertilizers and fertilizer coatings. | ||||||
| 75 | Adhesive tissue repair patch | US10971684 | 2004-10-22 | US20050054771A1 | 2005-03-10 | Louis Sehl; Olof Trollsas; Donald Wallace; David Toman; Frank DeLustro; Jacqueline Schroeder; George Chu |
| A method of tissue repair is provided using a biocompatible nonimmunogenic adhesive composition. The adhesive composition comprises collagen and a plurality of crosslinkable components having reactive functional groups thereon, with the functional groups selected so as to enable inter-reaction between the components, i.e., crosslinking. Kits for use in carrying out the method of the invention are also provided, as are pretreated surgically acceptable patches that have been coated with the aforementioned adhesive composition. | ||||||
| 76 | Sulfur containing polyhydroxyalkanoate compositions and method of production | US09932387 | 2001-08-17 | US06495152B2 | 2002-12-17 | Alexander Steinbuchel; Tina Lütke-Eversloh; Christian Ewering |
| A class of biopolymer including sulfur in the form of a thioester in the polymer backbone or a thioether in the polymer side chains has been developed. These are preferably produced by fermentation of bacteria with appropriate sulfur containing substrates, which are incorporated by a broad spectrum polyhydroxyalkanoate (“PHA”) polymerase. The sulfur-containing PHAs allow various applications and uses in industry. Representative embodiments of the applications of the sulfur-containing PHAs include their uses in the packaging industry, medicine, pharmacy, agriculture or food industry, as active agents or as coatings, packaging, or carriers. | ||||||
| 77 | Compositions and systems for forming crosslinked biomaterials and associated methods of preparation and use | US09883138 | 2001-06-15 | US06458889B1 | 2002-10-01 | Olof Mikael Trollsas; Donald G. Wallace; Frank A. DeLustro |
| Crosslinkable compositions are provided that readily crosslink in situ to provide biocompatible, nonimmunogenic crosslinked biomaterials. The compositions contain at least three biocompatible, nonimmunogenic components having reactive functional groups thereon, with the functional groups selected so as to enable inter-reaction between the components, i.e., crosslinking. In a preferred embodiment, a first component is polynucleophilic, a second component is polyelectrophilic, and at least one third component contains one or more functional groups reactive with the nucleophilic moieties one the first or second component. At least one of the components is a polyfunctional hydrophilic polymer; the other components may also comprise hydrophilic polymers, or they may be low molecular weight, typically hydrophobic, crosslinkers. Methods for preparing and using the compositions are also provided. Exemplary uses include tissue augmentation, biologically active agent delivery, bioadhesion, and prevention of adhesions following surgery or injury. | ||||||
| 78 | Reactive elastomeric block co-oligomer and lactam-block copolymers derived therefrom | US725061 | 1985-04-19 | US4843127A | 1989-06-27 | Murali K. Akkapeddi; David E. Bradley; Thomas D. Gallagher, deceased |
| The present invention includes a reactive elastomeric block co-oligomer; a copolymer containing a lactam, a co-catalyst/coupling agent, and the elastomeric block co-oligomer; and processes to make the block co-oligomer, and the copolymer.The reactive elastomeric block co-oligomer is the reaction product of a polycarboxylic acid, and a reactive moiety which can include a reactive polyether or a reactive polysulfide.The block co-oligomer of the present invention has been found to be useful to make a polymer containing lactam monomers, at least one coupling catalyst compound, and the block co-oligomer with the use of a catalyst.The present invention includes a process of forming the block co-oligomer of a polycarboyxlic acid and a reactive moiety. The reactive moiety can include a reactive polyether of a reactive polysulfide.The present invention further comprises a process of forming the block co-oligomer, and the process to form the lactam-block co-oligomer copolymer. | ||||||
| 79 | Hydroxyl or thiol terminated telomeric ethers | US42319473 | 1973-12-10 | US3900518A | 1975-08-19 | MILGROM JACK |
| Hydroxyl or thiol terminated alkylene ether telomers varying from liquids to thermoplastic solids and composed of one or more telomer moieties from cyclic ether taxogen joined through a carbon atom to a telogen moiety are prepared by telomerization of cyclic ether monomer with a primary or secondary aromatic amine as a telogen in the presence of catalyst of the double metal cyanide complex class. As a specific example, a hydroxyl terminated telomer is prepared by telomerization of propylene oxide with aniline using zinc hexacyanoferrate-diglyme complex as the telomerization catalyst.
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| 80 | Polyesters from the reaction of polyols and a mixture of mercaptoalkanoic and thioalkanoic acids | US29983272 | 1972-10-24 | US3857876A | 1974-12-31 | JONES F; WILLIAMS R; DOSS R |
| A polyester-polysulfide-polythiol curing agent which is the reaction product of a polyol and a mixture of a mercaptoalkanoic acid and a thiodialkanoic acid. This curing agent is employed to cure epoxy resins.
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