General Electric Company

Lockheed Martin Corporation

Global Life Sciences Solutions USA LLC

Donald Joseph Buckley

Eugene Pauling Boden

Scott Michael Miller

Stanton Earl Weaver, Jr

Weston Blaine Griffin

Reginald Donovan Smith

Kenneth Roger Conway

Chengkun Zhang

David B Cerutti

Ferenc Horkay

Richard Joseph Uriarte

Anshika Bajaj

Huabing Zheng

Yuzhuo Li

Earl Royce Tyre, Jr

Jason J Keleher

Daniel Joseph Brunelle

Steven Francis LeBoeuf

Paul Dean Sybert

Sterling B Brown

Arun Virupaksha Gowda

James Edward Pickett

Slawomir Rubinsztajn

Jimmy Lynn Webb

Kanakasabapathi Subramanian

Deborah Ann Haitko

Hongyi Zhou

Zhipeng Zhang

Richard Scott Bourgeois

Joseph Anthony Suriano

Tiberiu Mircea Siclovan

Murtuza Lokhandwalla

Chad Yates

Margaret Louise Blohm

Andrew Arthur Paul Burns

Russell William Craddock

Ajay Kapur

Kathryn Amanda Misner

Steven Paraszczak

Terry Lee Saunders

Georgia Dris Fishburn

Juan Alberto Rivas Cardona

Dana Ray Swala

A sampling assembly configured to be coupled to a sample source is provided. The sampling assembly is configured to facilitate aseptic sampling at one or more instances in time. The sampling assembly includes a first conduit having a first port and a second port, where the first port is configured to be coupled to the sample source, and where the second port is configured to be hermetically sealed. The sampling assembly further includes a plurality of sub-conduits having corresponding sub-ports, where each of the plurality of sub-conduits is operatively coupled to the first conduit at respective connection points, and where each of the sub-ports is in fluidic communication with the first conduit. Moreover, the sampling assembly includes a plurality of sampling kits, where each sampling kit of the plurality of sampling kits is operatively connected to a respective sub-port of a corresponding sub-conduit.

Systems and methods for aseptic sampling

Provided herein are methods and systems for rapid testing of films used in the manufacture of bioprocess bags. The methods described herein allow for determination of resistance to flexural fatigue while mimicking actual conditions in bioprocesses such as flexion and subsequent fatigue and failure of a bioprocess bag made of a film when it is placed on a rocking platform.

Method for testing of flexural fatigue resistance and associated system thereof

The present invention provides an insulated fluid conduit useful in facilities in which a hot fluid susceptible to deleterious phase changes in response to heat loss to a cold environment is transported. Such conduits may be particularly well suited to improve thermal control in subsea hydrocarbon production operations in which hot production fluids may undergo deleterious phase changes as a result of heat loss to the cold subsea environment. The fluid conduit includes an insulating material containing a silicone rubber and a phase change material such as octadecane. One or more barrier layers inhibit migration of the phase change material from the insulation layer and into the environment. In one or more embodiments, the phase change material is present as a microencapsulated phase change material.

Insulated fluid conduit

The present invention provides an insulated fluid conduit useful in facilities in which a hot fluid susceptible to one or more deleterious phase changes in response to heat loss to a cold environment is transported. Such conduits may be particularly well suited to improve thermal control in subsea hydrocarbon production operations. The fluid conduit includes an inner first insulating layer containing a first polymer matrix, and a first phase change material undergoing a phase change at T. The fluid conduit includes an outer second insulating layer containing a second polymer matrix, and a second phase change material undergoing a phase change at T, wherein Tis greater than T. One or more barrier layers inhibit migration of the phase change material from the insulation layers and into the environment. In one or more embodiments, the phase change material is present as a microencapsulated phase change material.

A sampling assembly configured to be coupled to a sample source and facilitate aseptic sampling at one or more instances in time is provided. Further, the sampling assembly includes a first conduit having first and second ports, where the first port is configured to be coupled to the sample source. The sampling assembly also includes a plurality of sub-conduits having corresponding sub-ports, where each of the plurality of sub-conduits is operatively coupled to the first conduit at respective connector junctions. Also, each of the sub-ports is in fluidic communication with the first conduit. The sampling assembly also includes a plurality of sampling kits and one or more pumping devices. Further, each sampling kit is operatively coupled to a respective sub-port of a corresponding sub-conduit. Moreover, the one or more pumping devices are operatively and aseptically coupled to the second port of the first conduit.

The present techniques provide a novel electrolyzer and methods for welding components of such electrolyzers. The techniques may use conductors, such as resistance wires, placed in paths around the internal structural features and edges of the components. The conductors may be incorporated into the components during manufacture by injection molding, or other molding techniques, or may be tacked or otherwise applied to the surface of the components after manufacture. When current, a field or other excitation is applied to the conductors, the plastic surrounding the wire is melted. If this plastic is in direct contact with an adjoining component, a strong, hermetic seal may be formed between the two components, including the internal structural features.

Electrolyzer assembly method and system

Apparatus for compressing tissue to be scanned for medical imaging is provided. The apparatus may comprise a compression membrane and a tensioning apparatus coupled to the membrane to apply a tensile force to the membrane to place the membrane in a taut condition during an imaging process. In one exemplary application that combines ultrasound scanning with X-ray mammography, the compressing apparatus enables accurate, reproducible ultrasound images reducing distortion and attenuation, which may otherwise be introduced as a consequence of such a combination of imaging processes.

Compression paddle membrane and tensioning apparatus for compressing tissue for medical imaging purposes

A sensor package and method are described. The sensor package includes an enclosure, a diaphragm coupled to the enclosure. The diaphragm is configured to receive vibrations from an ambient environment. Further, the sensor package includes a pressure sensing element disposed inside the enclosure, and a pressure transfer medium disposed inside the enclosure and proximate the pressure sensing element, where the pressure transfer medium includes a fluid, and a plurality of filler particles suspended in the fluid. The filler particles serve to reduce a coefficient of thermal expansion of the pressure transfer medium.

Sensor package and method

A lens and encapsulant made of an amorphous fluoropolymer for a light-emitting diode (LED) or diode laser, such as an ultraviolet (UV) LED (UVLED). A semiconductor diode die () is formed by growing a diode () on a substrate layer () such as sapphire. The diode die () is flipped so that it emits light () through the face () of the layer (). An amorphous fluoropolymer encapsulant encapsulates the emitting face of the diode die (), and may be shaped as a lens to form an integral encapsulant/lens. Or, a lens () of amorphous fluoropolymer may be joined to the encapsulant (). Additional joined or separate lenses () may also be used. The encapsulant/lens is transmissive to UV light as well as infrared light. Encapsulating methods are also provided.

Light-emitting diode (LED) with amorphous fluoropolymer encapsulant and lens

Block copolyestercarbonates may be prepared by first conducting a reaction between at least one of resorcinol or an alkyl- or haloresorcinol and at least one aromatic dicarboxylic acid dichloride, preferably isophthaloyl dichloride, terephthaloyl dichloride or a mixture thereof, to produce a hydroxy-terminated polyester intermediate, and then conducting a reaction of the intermediate with a carbonate precursor, preferably in the presence of a dihydroxy compound such as bisphenol A. The products have excellent physical properties, including a high degree of weatherability. They may be blended with other polymers such as polycarbonates, poly(alkylene carboxylates), polyarylates, polyetherimides, and addition polymers to improve the weatherability thereof.

Weatherable block copolyestercarbonates and blends containing them, and method

The multistage process for the chemical-mechanical planarization (CMP) of Cu commences with forming a primary aqueous or non-aqueous (e.g., using alcohols and ketones as non-aqueous carriers) slurry from (i) between about 0 and 7 wt-% of an oxidizer, (ii) between 0 and 7 wt-% of a chelating agent, (iii) between about 0 and 5 wt-% of a surfactant, (iv) between about 0.001 and 5 wt-% diamond particles having an average particle size not substantially above about 0.4 &mgr;, and (v) an amount of a pH adjustment agent so that the aqueous slurry has a pH of between about 3 and 10, and advantageously about 5). The Cu of the semiconductor wafer then is subjected to CMP using the primary aqueous slurry and then is subjected to a cleaning operation. Next, a secondary aqueous slurry from (i) between about 0 and 5 wt-% of an a hydroxyl amine compound, (ii) between about 0 and 7 wt-% of a chelating agent, (iii) between about 0 and 5 wt-% of a surfactant, (iv) between about 0.001 and 5 wt-% diamond particles having an average particle size not substantially above about 0.4 &mgr;, and (v) an amount of a pH adjustment agent so that the aqueous slurry has a pH of between about 4 and 10, and advantageously about 8.5 pH. The semiconductor wafer then is subjected to CMP using said secondary aqueous slurry. Thereafter, the semiconductor wafer again is subjected to a cleaning operation.

Diamond slurry for chemical-mechanical planarization of semiconductor wafers

The multistage process for the chemical-mechanical planarization (CMP) of Cu commences with forming a primary aqueous or non-aqueous (e.g., using alcohols and ketones as non-aqueous carriers) slurry from (i) between about 0 and 7 wt-% of an oxidizer, (ii) between 0 and 7 wt-% of one or more of a complexing agent or a passivating agent, (iii) between about 0 and 5 wt-% of a surfactant, (iv) between about 0.001 and 5 wt-% diamond particles having an average particle size not substantially above about 0.4 &mgr;m, and (v) an amount of a pH adjustment agent so that the aqueous slurry has a pH of between about 3 and 10, and advantageously about 5). The Cu of the semiconductor wafer then is subjected to CMP using the primary aqueous slurry and then is subjected to a cleaning operation. Next, a secondary aqueous slurry from (i) between about 0 and 7 wt-% of one or more a complexing agent or a passivating agent, (ii) between about 0 and 5 wt-% of a surfactant, (iii) between about 0.001 and 5 wt-% diamond particles having an average particle size not substantially above about 0.4 &mgr;m, and (iv) an amount of a pH adjustment agent so that the aqueous slurry has a pH of between about 4 and 10, and advantageously about 8.5 pH. The semiconductor wafer then is subjected to CMP using said secondary aqueous slurry. Thereafter, the semiconductor wafer again is subjected to a cleaning operation.

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Schenectady, NY, United States of America

Donald Joseph Buckley