Abstract: A common reference signal is used by a plurality of serially-connected power optimizers to manage a plurality of photovoltaic panels. It is determined whether an individual voltage output exceeds an individual limit. If so, a corresponding photovoltaic panel in the plurality of photovoltaic panels is adjusted to reduce the individual voltage output and the combined voltage output, where the combined voltage output is based at least in part on (a) the individual voltage output and (2) at least one other individual voltage output associated with another power optimizer. It is determined whether the combined voltage output relative to the common reference signal exceeds a maximum offset. If so, the corresponding photovoltaic panel in the plurality of photovoltaic panels is adjusted to reduce the individual voltage output and the combined voltage output.

Abstract: In various embodiments, a process for configuring or commissioning a solar power system includes receiving, at a controller, hardware identifiers of a plurality of power electronics modules to be configured. Each of the plurality of power electronics modules of at least a portion of the plurality of power electronics modules is associated with a corresponding photovoltaic panel. A hub is configured to wirelessly communicate with the plurality of power electronics modules. The controller is physically connected to the hub and communicates with the hub via wiring that also carries power from photovoltaic panels to an inverter. The process includes configuring, by the controller, the plurality of power electronics modules using the received hardware identifiers.

Abstract: The present discussion relates to structures and devices to facilitate application of an ultrasound therapy beam to a target anatomic region in a replicable manner. In certain aspects, adjustable positioning structures are described that allow a general probe positioning structure to be configured for a specific patient in a manner that allows the device to be used repeatedly to target the anatomic region, even when in non-clinical settings. In other aspects, a probe positioning structure is fabricated that is specific to a respective patient anatomy, such that use of the probe positioning structure provides repeatable targeting of the target anatomic region, even when in non-clinical settings.

Abstract: A machine for packing elongate bags for use with a waste disposal apparatus is disclosed herein. The machine comprises means for holding a reel of flexible tubing, the flexible tubing wound on the reel as a film having two parallel edges, the flexible tubing, when opened, forming a ring of elongate flexible tubing having an aperture at at least one end. The machine also comprises a pair of gripping means configured to engage and grip a region proximate to each edge of the film and draw the film of flexible tubing off of the reel, and a jig configured to be inserted into the aperture and hold a portion of the film in a ring around the jig, the jig configured to hold the film adjacent to and in engagement with the gripping means. Operation of the gripping means causes the film of elongate flexible tubing to be drawn over the jig and to be gathered in a ring of compacted flexible tubing around a base of the jig.

Abstract: The present discussion relates to structures and devices to facilitate application of an ultrasound therapy beam to a target anatomic region in a replicable manner. In certain aspects, adjustable positioning structures are described that allow a general probe positioning structure to be configured for a specific patient in a manner that allows the device to be used repeatedly to target the anatomic region, even when in non-clinical settings. In other aspects, a probe positioning structure is fabricated that is specific to a respective patient anatomy, such that use of the probe positioning structure provides repeatable targeting of the target anatomic region, even when in non-clinical settings.

Abstract: A common reference signal is used by a plurality of serially-connected power optimizers to manage a plurality of photovoltaic panels. It is determined whether an individual voltage output exceeds an individual limit. If so, a corresponding photovoltaic panel in the plurality of photovoltaic panels is adjusted to reduce the individual voltage output and the combined voltage output, where the combined voltage output is based at least in part on (a) the individual voltage output and (2) at least one other individual voltage output associated with another power optimizer. It is determined whether the combined voltage output relative to the common reference signal exceeds a maximum offset. If so, the corresponding photovoltaic panel in the plurality of photovoltaic panels is adjusted to reduce the individual voltage output and the combined voltage output.

Abstract: A secondary payload bridge for a payload adapter is disclosed and includes a body portion, plurality of payload ports, and a secondary payload port. The plurality of attachment points are connected to the body portion of the secondary payload bridge. The plurality of attachment points are configured to removably attach the secondary payload bridge to the payload adapter to allow for clockable positioning of the secondary payload bridge around a circumference of the payload adapter. The secondary payload port is connected to the body portion. The secondary payload port is configured to releasably attach to a corresponding secondary payload.

Abstract: The present discussion relates to structures and devices to facilitate application of an ultrasound therapy beam to a target anatomic region in a replicable manner. In certain aspects, adjustable positioning structures are described that allow a general probe positioning structure to be configured for a specific patient in a manner that allows the device to be used repeatedly to target the anatomic region, even when in non-clinical settings. In other aspects, a probe positioning structure is fabricated that is specific to a respective patient anatomy, such that use of the probe positioning structure provides repeatable targeting of the target anatomic region, even when in non-clinical settings.

Abstract: The present disclosure relates to the manufacture and use of redox electrodes and their use in cell lysis. In certain embodiments, the redox electrodes are manufactured using a hybrid material approach, such as using a redox polymer in combination with a support substrate, such as cellulose fibers or paper. In certain implementations, the redox electrodes are suitable for use at voltages greater than 25 Volts.

Abstract: A payload adapter configured to removably attach to one or more payload bridges. The payload adapter includes a forward open end defined by a forward ring, an aft open end defined by an aft ring, a plurality of truss supports connecting the forward ring and the aft ring to one another, and a plurality of mounting fixtures disposed around a circumference the payload adapter. The mounting fixtures are each configured to releasably attach to a secondary payload bridge.

Abstract: An improved exclusion barrier including a plurality of elongate members extending in a generally upright condition between a sea floor and a sea surface. The elongate members are improved to provide a more uniform surface area for the prevention of sharks passing through upper portions of the barrier and maximizing the exclusion capabilities of the overall barrier network. The elongate members include, in addition to permanent magnets, hydro-electric power generation mechanisms for powering electro-magnets within the elongate members to produce a stronger electro-magnetic deterrent field across the barrier network, and also include telescoping mechanisms to allow for a variance in length of each member in coordination with changing wave and water levels and to provide additional pump action for hydro-electric power generation within each elongate member. The exclusion barrier is also secured to the sea floor by an anchoring base having evenly spaced anchoring locations.

Abstract: A system for isolating a target molecule from a bioprocess fluid includes a single-use disposable separation device having a plurality of perimeter-bonded layers defining one or more mesofluidic channels of the separation device, wherein each layer includes a biocompatible polymer material, wherein the separation device is configured to separate at least a portion of particles from the bioprocess fluid to generate a substantially clarified bioprocess fluid, and a chromatography system fluidically coupled at the outflow of the separation device in a configuration for further processing the clarified bioprocess fluid.

Abstract: Fluid applicator assemblies which can be attached to or fabricated integrally with a blowing apparatus such as a leaf blower as a source of flowing air to atomize and eject atomized liquids into spaces and/or onto surfaces may include a nozzle having a nozzle body. At least one air flow cavity may be provided in the nozzle body. An air inlet slot may extend through the nozzle body and may be disposed in fluid communication with the at least one air flow cavity. A fluid ejection portion may be carried by the nozzle body. The fluid ejection portion may include an ejection head support extending from the nozzle body. A fluid ejection head may be carried by the ejection head support. A tube opening may extend through the fluid ejection portion. A fluid ejection slot may be provided in the fluid ejection head and disposed in fluid communication with the tube opening. A liquid container may be disposed in fluid communication with the fluid ejection slot through the tube opening.

Abstract: A method of eluting biomolecules, such as nucleic acids from a biological sample by electroelution is provided. An example of a method includes various steps, such as loading the biological sample to a device comprising a housing, at least two conductive redox polymer electrodes operationally coupled to the housing and a biomolecule impermeable layer disposed on at least one of the electrodes. The loading of sample is followed by initiating an electrical connection to generate an electric field strength sufficient to elute biomolecules from the biological sample; and eluting the biomolecules from the biological sample.

Abstract: A system for isolating a target molecule from a bioprocess fluid includes a single-use disposable separation device having a plurality of perimeter-bonded layers defining one or more mesofluidic channels of the separation device, wherein each layer includes a biocompatible polymer material, wherein the separation device is configured to separate at least a portion of particles from the bioprocess fluid to generate a substantially clarified bioprocess fluid, and a chromatography system fluidically coupled at the outflow of the separation device in a configuration for further processing the clarified bioprocess fluid.

Abstract: A payload adapter configured to removably attach to one or more payload bridges. The payload adapter includes a forward open end defined by a forward ring, an aft open end defined by an aft ring, a plurality of truss supports connecting the forward ring and the aft ring to one another, and a plurality of mounting fixtures disposed around a circumference the payload adapter. The mounting fixtures are each configured to releasably attach to a secondary payload bridge.

Abstract: A secondary payload bridge for a payload adapter is disclosed and includes a body portion, plurality of payload ports, and a secondary payload port. The plurality of attachment points are connected to the body portion of the secondary payload bridge. The plurality of attachment points are configured to removably attach the secondary payload bridge to the payload adapter to allow for clockable positioning of the secondary payload bridge around a circumference of the payload adapter. The secondary payload port is connected to the body portion. The secondary payload port is configured to releasably attach to a corresponding secondary payload.

Abstract: A system includes a bacteria culture array that includes a plurality of chambers each configured to receive a portion of a sample that includes bacteria. Each individual chamber of the plurality of chambers includes a chamber opening configured to permit access of the portion of the sample to the individual chamber. The system also includes one or more sensors configured to collect data from the individual chamber. The sensors are configured to contact the sample. Additionally, the system includes a monitoring and analysis system that includes a processor configured to receive the data from the one or more sensors at a first time and a second time, compare the data received at the second time to the data received at the first time, and identify a portion of the plurality of chambers of the bacteria culture array based on the comparing.