Western Washington University

United States of America

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IPC Class
C12N 1/12 - Unicellular algaeCulture media therefor 4
C12P 7/26 - Ketones 4
C12P 7/64 - FatsFatty oilsEster-type waxesHigher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl groupOxidised oils or fats 4
C07D 303/32 - Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by aldehydo- or ketonic radicals 3
A61K 8/33 - Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen 2
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Status
Pending 3
Registered / In Force 18

1.

INERT ENVIRONMENT SLEEVE ADAPTER

      
Application Number US2024020738
Publication Number 2024/197043
Status In Force
Filing Date 2024-03-20
Publication Date 2024-09-26
Owner WESTERN WASHINGTON UNIVERSITY (USA)
Inventor O'Neil, Greg

Abstract

Many chemicals are sensitive to or can react with compounds in the air. For example, many chemicals can react to water vapor and oxygen as well as trace gases carbon dioxide, ammonia, and hydrogen sulfide. Chemicals are typically packaged in a container. A device, called an adapter, is presented to provide an inert environment when working with reactive chemicals. The adapter is fitted on the container and allows for the establishment of inert environment that surrounds the opening of the container.

IPC Classes  ?

  • B01J 19/14 - Production of inert gas mixturesUse of inert gases in general
  • B01J 19/02 - Apparatus characterised by being constructed of material selected for its chemically-resistant properties
  • B01L 1/00 - EnclosuresChambers
  • B01L 3/12 - Gas jars or cylinders
  • B65D 85/84 - Containers, packaging elements or packages, specially adapted for particular articles or materials for corrosive chemicals

2.

PARTICLE FLOW CONTROL SYSTEM

      
Application Number US2023031486
Publication Number 2024/096949
Status In Force
Filing Date 2023-08-30
Publication Date 2024-05-10
Owner
  • THE UNIVERSITY OF TULSA (USA)
  • WESTERN WASHINGTON UNIVERSITY (USA)
  • BOISE STATE UNIVERSITY (USA)
Inventor
  • Karimi, Soroor
  • Goel, Nipun
  • Otanicar, Todd

Abstract

A material flow control system. In one embodiment, the flow control system includes an elongated flow control body, the body having an axial passage therethrough, wherein the axial passage is in communication with a heat exchanger and in communication with low temperature storage. Each of a plurality of fingers are received in an opening passing through the flow control body into the axial passage, each opening at an angle to the axial passage, wherein the plurality of fingers together form a nozzle for passage of heat transfer material therethrough. A mechanism actuates movement of each of said plurality of fingers in said elongated flow control body.

IPC Classes  ?

  • B05B 1/32 - Nozzles, spray heads or other outlets, with or without auxiliary devices such as valves, heating means designed to control volume of flow, e.g. with adjustable passages in which a valve member forms part of the outlet opening
  • B29C 45/23 - Feed stopping equipment
  • F16K 3/02 - Gate valves or sliding valves, i.e. cut-off apparatus with closing members having a sliding movement along the seat for opening and closing with flat sealing facesPackings therefor
  • F16K 31/58 - Mechanical actuating means comprising a movable discharge-nozzle
  • F04F 5/46 - Arrangements of nozzles
  • F03G 6/06 - Devices for producing mechanical power from solar energy with solar energy concentrating means
  • F24S 20/20 - Solar heat collectors for receiving concentrated solar energy, e.g. receivers for solar power plants

3.

ALKENONE-BASED FORMULATIONS FOR TOPICAL APPLICATIONS

      
Application Number 18386498
Status Pending
Filing Date 2023-11-02
First Publication Date 2024-04-18
Owner
  • Woods Hole Oceanographic Institution (USA)
  • Western Washington University (USA)
Inventor
  • O'Neil, Gregory W.
  • Reddy, Christopher M.

Abstract

The use of long-chain alkenones to impart desired characteristics in personal care compositions for topical applications is described. The preparation of mixtures long-chain alkenones and synthetic derivatives thereof is presented. Examples of compositions include abrasive soaps, with alkenones serving as natural exfoliating agents. Alkenones and their derivatives can serve as emollients, occlusive agents, stabailizing agents, binding agents, thickening agents, surfactants, and antimicrobials.

IPC Classes  ?

  • A61K 8/33 - Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
  • A61K 8/35 - Ketones, e.g. quinones, benzophenone
  • A61K 8/36 - Carboxylic acidsSalts or anhydrides thereof
  • A61K 8/37 - Esters of carboxylic acids
  • A61K 8/41 - Amines
  • A61K 8/44 - Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfurSalts, esters or N-acylated derivatives thereof
  • A61K 8/55 - Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing phosphorus
  • A61K 8/9711 - Phaeophycota or Phaeophyta [brown algae], e.g. Fucus
  • A61K 8/9717 - Rhodophycota or Rhodophyta [red algae], e.g. Porphyra
  • A61K 8/9728 - Fungi, e.g. yeasts
  • A61K 8/9741 - Pteridophyta [ferns]
  • A61K 8/9761 - Cupressaceae [Cypress family], e.g. juniper or cypress
  • A61K 8/9767 - Pinaceae [Pine family], e.g. pine or cedar
  • A61K 8/9771 - Ginkgophyta, e.g. Ginkgoaceae [Ginkgo family]
  • A61K 8/9789 - Magnoliopsida [dicotyledons]
  • A61K 8/9794 - Liliopsida [monocotyledons]
  • A61Q 5/00 - Preparations for care of the hair
  • A61Q 19/00 - Preparations for care of the skin

4.

DISTAL-SCREW GUIDING SYSTEM FOR INTERLOCKING INTRAMEDULLARY NAIL IMPLANTS

      
Application Number 18046800
Status Pending
Filing Date 2022-10-14
First Publication Date 2024-04-18
Owner WESTERN WASHINGTON UNIVERSITY (USA)
Inventor
  • Al-Qudah, Sura
  • Al-Qudah, Ala' K.
  • Smith, Levi

Abstract

A screw locating system including an intramedullary nail, a locating hole at the distal end of the intramedullary nail, a locator pin including a hollow section, and a locating end configured to fit in the locating hole, a cap configured to fill in the locating hole when the locator pin is in the locating hole, a screw configured to securely hold the locator pin, and a jig configured to guide a user to locate at least one distal screw at the distal end of the intramedullary nail.

IPC Classes  ?

5.

Systems and methods for locating tagged objects in remote regions

      
Application Number 17995399
Grant Number 11808873
Status In Force
Filing Date 2021-03-31
First Publication Date 2023-04-20
Grant Date 2023-11-07
Owner WESTERN WASHINGTON UNIVERSITY (USA)
Inventor
  • Wallin, David
  • Bunn, Andrew
  • Lund, John

Abstract

Systems and methods for locating tagged objects in remote regions are presented herein, in one embodiment, a method of locating tagged objects in remote regions includes creating a signal strength probability density map by. The method also includes transmitting first packets of data from at least one first tag to a plurality of stations and determining, by a plurality of stations, received signal strength indicator (RSSI) for received first packets of data. The method also includes transmitting, by the plurality of stations, the RSSI to an uplink node; and transmitting, by the uplink node, the RSSI to a database. The method further includes determining, by the database, the signal strength probability density map representative of probabilistic locations of the at least one first tag; and transmitting second packets of data from a second tag to the plurality of stations. Based on the signal strength probability density map and the second packets of data from the second tag, a location of the second tag is determined.

IPC Classes  ?

  • G01S 5/02 - Position-fixing by co-ordinating two or more direction or position-line determinationsPosition-fixing by co-ordinating two or more distance determinations using radio waves
  • G01S 5/00 - Position-fixing by co-ordinating two or more direction or position-line determinationsPosition-fixing by co-ordinating two or more distance determinations

6.

Alkenone-based formulations for topical applications

      
Application Number 17397256
Grant Number 11839675
Status In Force
Filing Date 2021-08-09
First Publication Date 2021-11-25
Grant Date 2023-12-12
Owner WESTERN WASHINGTON UNIVERSITY (USA)
Inventor
  • O'Neil, Gregory W.
  • Reddy, Christopher M.

Abstract

The use of long-chain alkenones to impart desired characteristics in personal care compositions for topical applications is described. The preparation of mixtures long-chain alkenones and synthetic derivatives thereof is presented. Examples of compositions include abrasive soaps, with alkenones serving as natural exfoliating agents. Alkenones and their derivatives can serve as emollients, occlusive agents, encapsulating agents, stabilizing agents, binding agents, thickening agents, surfactants, and antimicrobials.

IPC Classes  ?

  • A61K 8/33 - Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
  • A61K 8/37 - Esters of carboxylic acids
  • A61K 8/41 - Amines
  • A61K 8/55 - Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing phosphorus
  • A61Q 19/00 - Preparations for care of the skin
  • A61K 8/44 - Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfurSalts, esters or N-acylated derivatives thereof
  • A61K 8/9711 - Phaeophycota or Phaeophyta [brown algae], e.g. Fucus
  • A61K 8/9717 - Rhodophycota or Rhodophyta [red algae], e.g. Porphyra
  • A61K 8/9728 - Fungi, e.g. yeasts
  • A61K 8/9741 - Pteridophyta [ferns]
  • A61K 8/9761 - Cupressaceae [Cypress family], e.g. juniper or cypress
  • A61K 8/9767 - Pinaceae [Pine family], e.g. pine or cedar
  • A61K 8/9771 - Ginkgophyta, e.g. Ginkgoaceae [Ginkgo family]
  • A61K 8/9789 - Magnoliopsida [dicotyledons]
  • A61K 8/9794 - Liliopsida [monocotyledons]
  • A61K 8/35 - Ketones, e.g. quinones, benzophenone
  • A61K 8/36 - Carboxylic acidsSalts or anhydrides thereof
  • A61Q 5/00 - Preparations for care of the hair

7.

Use of marine algae for co-producing alkenones, alkenone derivatives, and co-products

      
Application Number 17388298
Grant Number 11634738
Status In Force
Filing Date 2021-07-29
First Publication Date 2021-11-18
Grant Date 2023-04-25
Owner
  • Woods Hole Oceanographic Institution (USA)
  • Western Washington University (USA)
  • Marine Biological Laboratory (USA)
Inventor
  • Reddy, Christopher M.
  • O'Neil, Gregory W.
  • Lindell, Scott R.

Abstract

Isochrysis.

IPC Classes  ?

  • C12P 7/64 - FatsFatty oilsEster-type waxesHigher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl groupOxidised oils or fats
  • C12P 7/26 - Ketones
  • C07D 303/32 - Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by aldehydo- or ketonic radicals
  • C12N 1/12 - Unicellular algaeCulture media therefor
  • C10L 1/185 - EthersAcetalsKetalsAldehydesKetones
  • C10L 1/19 - Esters
  • C10L 1/18 - Organic compounds containing oxygen
  • C12P 7/649 - Biodiesel, i.e. fatty acid alkyl esters
  • C11C 3/00 - Fats, oils or fatty acids obtained by chemical modification of fats, oils or fatty acids, e.g. by ozonolysis
  • C07C 49/00 - KetonesKetenesDimeric ketenesKetonic chelates

8.

SYSTEMS AND METHODS FOR LOCATING TAGGED OBJECTS IN REMOTE REGIONS

      
Application Number US2021025124
Publication Number 2021/202691
Status In Force
Filing Date 2021-03-31
Publication Date 2021-10-07
Owner WESTERN WASHINGTON UNIVERSITY (USA)
Inventor
  • Wallin, David
  • Bunn, Andy
  • Lung, John

Abstract

Systems and methods for locating tagged objects in remote regions are presented herein, in one embodiment, a method of locating tagged objects in remote regions includes creating a signal strength probability density map by. The method also includes transmitting first packets of data from at least one first tag to a plurality of stations and determining, by a plurality of stations, received signal strength indicator (RSSI) for received first packets of data. The method also includes transmitting, by the plurality of stations, the RSSI to an uplink node; and transmitting, by the uplink node, the RSSI to a database. The method further includes determining, by the database, the signal strength probability density map representative of probabilistic locations of the at least one first tag; and transmitting second packets of data from a second tag to the plurality of stations. Based on the signal strength probability density map and the second packets of data from the second tag, a location of the second tag is determined.

IPC Classes  ?

  • G01S 11/06 - Systems for determining distance or velocity not using reflection or reradiation using radio waves using intensity measurements
  • H04W 4/029 - Location-based management or tracking services
  • G01S 5/02 - Position-fixing by co-ordinating two or more direction or position-line determinationsPosition-fixing by co-ordinating two or more distance determinations using radio waves

9.

BENZOXAZINE BLENDS

      
Application Number 17044748
Status Pending
Filing Date 2019-04-01
First Publication Date 2021-05-20
Owner WESTERN WASHINGTON UNIVERSITY (USA)
Inventor
  • Rider, David Allen
  • Brown, Emily Ann
  • Nadeem, Ayesha

Abstract

Provided herein are blends of benzoxazine-containing monomers with polymer having one or more leaving groups, such as tosylated polymers (e.g., tosylated polyethylene glycol (PEG)); or blends of benzoxazine-containing monomers with particles/fibers having one or more leaving groups.

IPC Classes  ?

  • C08F 283/06 - Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass on to polyethers, polyoxymethylenes or polyacetals
  • C07D 413/06 - Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
  • C08K 7/14 - Glass
  • C08K 7/06 - Elements
  • C08K 3/04 - Carbon

10.

ALKENONES AS PHASE CHANGE MATERIALS AND APPLICATIONS THEREOF

      
Application Number US2019035864
Publication Number 2019/236902
Status In Force
Filing Date 2019-06-06
Publication Date 2019-12-12
Owner
  • WOODS HOLE OCEANOGRAPHIC INSTITUTION (USA)
  • WESTERN WASHINGTON UNIVERSITY (USA)
Inventor
  • O'Neil, Gregory W.
  • Reddy, Christopher M.

Abstract

The present disclosure describes renewable technology applications for a unique suite of algal lipids known as polyunsaturated long-chain alkenones. The present disclosure describes the use of alkenones as phase change materials. Unmodified alkenone mixtures display good melting ranges and latent heat enthalpy values, making these compounds useful as environmentally friendly phase change materials.

IPC Classes  ?

  • C07C 45/65 - Preparation of compounds having C=O groups bound only to carbon or hydrogen atomsPreparation of chelates of such compounds by reactions not involving the formation of C=O groups by splitting-off hydrogen atoms or functional groupsPreparation of compounds having C=O groups bound only to carbon or hydrogen atomsPreparation of chelates of such compounds by reactions not involving the formation of C=O groups by hydrogenolysis of functional groups

11.

BENZOXAZINE BLENDS

      
Application Number US2019025186
Publication Number 2019/195170
Status In Force
Filing Date 2019-04-01
Publication Date 2019-10-10
Owner WESTERN WASHINGTON UNIVERSITY (USA)
Inventor
  • Rider, David Allen
  • Brown, Emily Ann
  • Nadeem, Ayesha

Abstract

Provided herein are blends of benzoxazine-containing monomers with polymer having one or more leaving groups, such as tosylated polymers (e.g., tosylated polyethylene glycol (PEG)); or blends of benzoxazine-containing monomers with particles/fibers having one or more leaving groups.

IPC Classes  ?

  • C08G 73/00 - Macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen, with or without oxygen or carbon, not provided for in groups
  • C08J 3/00 - Processes of treating or compounding macromolecular substances
  • C08K 9/00 - Use of pretreated ingredients
  • C08L 79/04 - Polycondensates having nitrogen-containing heterocyclic rings in the main chainPolyhydrazidesPolyamide acids or similar polyimide precursors
  • C09D 179/00 - Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen, with or without oxygen, or carbon only, not provided for in groups
  • H01B 3/30 - Insulators or insulating bodies characterised by the insulating materialsSelection of materials for their insulating or dielectric properties mainly consisting of organic substances plasticsInsulators or insulating bodies characterised by the insulating materialsSelection of materials for their insulating or dielectric properties mainly consisting of organic substances resinsInsulators or insulating bodies characterised by the insulating materialsSelection of materials for their insulating or dielectric properties mainly consisting of organic substances waxes

12.

Use of marine algae for co-producing alkenones, alkenone derivatives, and co-products

      
Application Number 16259339
Grant Number 11118199
Status In Force
Filing Date 2019-01-28
First Publication Date 2019-05-30
Grant Date 2021-09-14
Owner
  • WOODS HOLE OCEANOGRAPHIC INSTITUTION (USA)
  • WESTERN WASHINGTON UNIVERSITY (USA)
  • MARINE BIOLOGICAL LABORATORY (USA)
Inventor
  • Reddy, Christopher M.
  • O'Neil, Gregory W.
  • Lindell, Scott R.

Abstract

Isochrysis.

IPC Classes  ?

  • C12P 7/64 - FatsFatty oilsEster-type waxesHigher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl groupOxidised oils or fats
  • C12N 1/12 - Unicellular algaeCulture media therefor
  • C07D 303/32 - Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by aldehydo- or ketonic radicals
  • C12P 7/26 - Ketones
  • C10L 1/185 - EthersAcetalsKetalsAldehydesKetones
  • C10L 1/19 - Esters
  • C10L 1/18 - Organic compounds containing oxygen
  • C11C 3/00 - Fats, oils or fatty acids obtained by chemical modification of fats, oils or fatty acids, e.g. by ozonolysis
  • C07C 49/00 - KetonesKetenesDimeric ketenesKetonic chelates

13.

Use of marine algae for co-producing alkenones, alkenone derivatives, and co-products

      
Application Number 15949983
Grant Number 10208321
Status In Force
Filing Date 2018-04-10
First Publication Date 2018-08-16
Grant Date 2019-02-19
Owner
  • Woods Hole Oceanographic Institution (USA)
  • Western Washington University (USA)
Inventor
  • Reddy, Christopher M.
  • O'Neil, Gregory W.

Abstract

Isochrysis.

IPC Classes  ?

  • C12P 7/26 - Ketones
  • C12P 7/64 - FatsFatty oilsEster-type waxesHigher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl groupOxidised oils or fats
  • C07D 303/32 - Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by aldehydo- or ketonic radicals
  • C12N 1/12 - Unicellular algaeCulture media therefor

14.

Photoluminescent semiconductor nanocrystal-based luminescent solar concentrators

      
Application Number 15952123
Grant Number 10317602
Status In Force
Filing Date 2018-04-12
First Publication Date 2018-08-16
Grant Date 2019-06-11
Owner
  • Western Washington University (USA)
  • University of Washington Through Its Center For Commercialization (USA)
Inventor
  • Patrick, David
  • Gilbertson, John
  • Mcdowall, Stephen
  • Erickson, Christian
  • Gamelin, Daniel R.
  • Bradshaw, Liam
  • Mclaurin, Emily Jane
  • Knowles, Kathryn E.

Abstract

The present disclosure describes luminescent solar concentrators that include photoluminescent nanoparticles. The photoluminescent nanoparticles include a semiconductor nanocrystal that sensitizes the luminescence of a defect. The defect can include, for example, an atom, a cluster of atoms, or a lattice vacancy. The defect can be incorporated into the semiconductor nanocrystal, adsorbed onto, or otherwise associated with the surface of the semiconductor nanocrystal.

IPC Classes  ?

  • F21V 8/00 - Use of light guides, e.g. fibre optic devices, in lighting devices or systems
  • G02B 19/00 - Condensers
  • H01L 31/055 - Optical elements directly associated or integrated with the PV cell, e.g. light-reflecting means or light-concentrating means where light is absorbed and re-emitted at a different wavelength by the optical element directly associated or integrated with the PV cell, e.g. by using luminescent material, fluorescent concentrators or up-conversion arrangements
  • C09K 11/02 - Use of particular materials as binders, particle coatings or suspension media therefor
  • C09K 11/56 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing inorganic luminescent materials containing sulfur
  • C09K 11/58 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing inorganic luminescent materials containing copper, silver or gold
  • C09K 11/77 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing inorganic luminescent materials containing rare earth metals
  • C09K 11/88 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing inorganic luminescent materials containing selenium, tellurium or unspecified chalcogen elements
  • H01L 31/0232 - Optical elements or arrangements associated with the device
  • B82Y 20/00 - Nanooptics, e.g. quantum optics or photonic crystals
  • B82Y 40/00 - Manufacture or treatment of nanostructures

15.

Nanoscale nickel phosphide catalysts for hydrotreatment

      
Application Number 15306468
Grant Number 10406509
Status In Force
Filing Date 2016-04-22
First Publication Date 2017-07-06
Grant Date 2019-09-10
Owner Western Washington University (USA)
Inventor Bussell, Mark E.

Abstract

2P) particles supported on high-surface area metal oxides (e.g., silica, alumina, amorphous silica-alumina), in a manner that is compatible with conditions employed in commercial hydrotreating units. The catalyst synthesis includes impregnation, drying, and in situ reduction, and can provide highly active catalysts for the removal of S and N impurities from crude oil fractions.

IPC Classes  ?

  • B01J 21/02 - Boron or aluminiumOxides or hydroxides thereof
  • B01J 21/04 - Alumina
  • B01J 21/08 - Silica
  • B01J 27/16 - PhosphorusCompounds thereof containing oxygen
  • B01J 27/185 - PhosphorusCompounds thereof with iron group metals or platinum group metals
  • C01B 25/08 - Other phosphides
  • B01J 37/02 - Impregnation, coating or precipitation
  • B01J 37/18 - Reducing with gases containing free hydrogen
  • C10G 45/00 - Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
  • C10G 45/06 - Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbonsHydrofinishing characterised by the catalyst used containing nickel or cobalt metal, or compounds thereof
  • B01J 37/08 - Heat treatment
  • B01J 37/20 - Sulfiding
  • B01J 35/00 - Catalysts, in general, characterised by their form or physical properties
  • B01J 35/10 - Solids characterised by their surface properties or porosity

16.

Photoluminescent semiconductor nanocrystal-based luminescent solar concentrators

      
Application Number 14902113
Grant Number 09964680
Status In Force
Filing Date 2014-07-01
First Publication Date 2016-11-10
Grant Date 2018-05-08
Owner
  • Western Washington University (USA)
  • University of Washington through its Center for Commercialization (USA)
Inventor
  • Patrick, David
  • Gilbertson, John
  • Mcdowall, Stephen
  • Erickson, Christian
  • Gamelin, Daniel R.
  • Bradshaw, Liam
  • Mclaurin, Emily Jane
  • Knowles, Kathryn E.

Abstract

The present disclosure describes luminescent solar concentrators that include photoluminescent nanoparticles. The photoluminescent nanoparticles include a semiconductor nanocrystal that sensitizes the luminescence of a defect. The defect can include, for example, an atom, a cluster of atoms, or a lattice vacancy. The defect can be incorporated into the semiconductor nanocrystal, adsorbed onto, or otherwise associated with the surface of the semiconductor nanocrystal.

IPC Classes  ?

  • F21V 8/00 - Use of light guides, e.g. fibre optic devices, in lighting devices or systems
  • H01L 31/055 - Optical elements directly associated or integrated with the PV cell, e.g. light-reflecting means or light-concentrating means where light is absorbed and re-emitted at a different wavelength by the optical element directly associated or integrated with the PV cell, e.g. by using luminescent material, fluorescent concentrators or up-conversion arrangements
  • H01L 31/0232 - Optical elements or arrangements associated with the device
  • G02B 19/00 - Condensers
  • C09K 11/02 - Use of particular materials as binders, particle coatings or suspension media therefor
  • C09K 11/56 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing inorganic luminescent materials containing sulfur
  • C09K 11/58 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing inorganic luminescent materials containing copper, silver or gold
  • C09K 11/77 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing inorganic luminescent materials containing rare earth metals
  • C09K 11/88 - Luminescent, e.g. electroluminescent, chemiluminescent, materials containing inorganic luminescent materials containing selenium, tellurium or unspecified chalcogen elements
  • B82Y 20/00 - Nanooptics, e.g. quantum optics or photonic crystals
  • B82Y 40/00 - Manufacture or treatment of nanostructures

17.

NANOSCALE NICKEL PHOSPHIDE CATALYSTS FOR HYDROTREATMENT

      
Application Number US2016029009
Publication Number 2016/172603
Status In Force
Filing Date 2016-04-22
Publication Date 2016-10-27
Owner WESTERN WASHINGTON UNIVERSITY (USA)
Inventor Bussell, Mark, E.

Abstract

This present disclosure is directed to methods for the preparation of a hydrotreatment catalyst, such as nanoscale nickel phosphide (i.e., Ni2P) particles supported on high-surface area metal oxides (e.g., silica, alumina, amorphous silica- alumina), in a manner that is compatible with conditions employed in commercial hydrotreating units. The catalyst synthesis includes impregnation, drying, and in situ reduction, and can provide highly active catalysts for the removal of S and N impurities from crude oil fractions.

IPC Classes  ?

  • B01J 27/185 - PhosphorusCompounds thereof with iron group metals or platinum group metals
  • B01J 27/00 - Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogenCatalysts comprising carbon compounds
  • B01J 27/14 - PhosphorusCompounds thereof
  • C01B 25/00 - PhosphorusCompounds thereof
  • C01B 25/08 - Other phosphides

18.

Use of marine algae for co-producing alkenones, alkenone derivatives, and co-products

      
Application Number 14599460
Grant Number 09970034
Status In Force
Filing Date 2015-01-17
First Publication Date 2015-05-21
Grant Date 2018-05-15
Owner
  • Woods Hole Oceanographic Institution (USA)
  • Western Washington University (USA)
  • Marine Biological Laboratory (USA)
Inventor
  • Reddy, Christopher M.
  • O'Neil, Gregory W.
  • Lindell, Scott R.

Abstract

Isochrysis.

IPC Classes  ?

  • C12N 1/26 - Processes using, or culture media containing, hydrocarbons
  • C12N 1/12 - Unicellular algaeCulture media therefor
  • C12P 7/64 - FatsFatty oilsEster-type waxesHigher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl groupOxidised oils or fats
  • C12P 7/26 - Ketones
  • C07D 303/32 - Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by aldehydo- or ketonic radicals

19.

PHOTOLUMINESCENT SEMICONDUCTOR NANOCRYSTAL-BASED LUMINESCENT SOLAR CONCENTRATORS

      
Application Number US2014045130
Publication Number 2015/002995
Status In Force
Filing Date 2014-07-01
Publication Date 2015-01-08
Owner
  • WESTERN WASHINGTON UNIVERSITY (USA)
  • UNIVERSITY OF WASHINGTON THROUGH ITS CENTER FOR COMMERCIALIZATION (USA)
Inventor
  • Patrick, David
  • Gilbertson, John
  • Mcdowall, Stephen
  • Erickson, Christian
  • Gamelin, Daniel, R.
  • Bradshaw, Liam
  • Mclaurin, Emily, Jane
  • Knowles, Kathryn, E.

Abstract

The present disclosure describes luminescent solar concentrators that include photoluminescent nanoparticles. The photoluminescent nanoparticles include a semiconductor nanocrystal that sensitizes the luminescence of a defect. The defect can include, for example, an atom, a cluster of atoms, or a lattice vacancy. The defect can be incorporated into the semiconductor nanocrystal, adsorbed onto, or otherwise associated with the surface of the semiconductor nanocrystal.

IPC Classes  ?

  • H01L 29/36 - Semiconductor bodies characterised by the concentration or distribution of impurities

20.

Use of marine algae for producing polymers

      
Application Number 13298576
Grant Number 09879288
Status In Force
Filing Date 2011-11-17
First Publication Date 2012-06-28
Grant Date 2018-01-30
Owner
  • Woods Hole Oceanographic Institution (USA)
  • Marine Biological Laboratory (USA)
  • Western Washington University (USA)
Inventor
  • Lindell, Scott R.
  • Reddy, Christopher M.
  • O'Neil, Gregory W.

Abstract

In certain aspects, the disclosure provides methods for producing polymers from alkenone-producing algae, such as algae species of the Isochrysis family.

IPC Classes  ?

  • C12P 5/02 - Preparation of hydrocarbons acyclic
  • C12P 7/26 - Ketones
  • C12N 1/12 - Unicellular algaeCulture media therefor
  • C12P 7/64 - FatsFatty oilsEster-type waxesHigher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl groupOxidised oils or fats

21.

FACING THE FUTURE

      
Serial Number 78223828
Status Registered
Filing Date 2003-03-10
Registration Date 2005-06-07
Owner WESTERN WASHINGTON UNIVERSITY ()
NICE Classes  ? 41 - Education, entertainment, sporting and cultural services

Goods & Services

educational services, namely, preparing and disseminating materials of others for use in teaching students and the public about global issues; educational services, namely, conducting seminars and training to educators and the public about global issues and solutions and distributing course materials in connection therewith