Abstract: In an aspect, provided is an alkaline rechargeable battery comprising: i) a battery container sealed against the release of gas up to at least a threshold gas pressure, ii) a volume of an aqueous alkaline electrolyte at least partially filling the container to an electrolyte level; iii) a positive electrode containing positive active material and at least partially submerged in the electrolyte; iv) an iron negative electrode at least partially submerged in the electrolyte, the iron negative electrode comprising iron active material; v) a separator at least partially submerged in the electrolyte provided between the positive electrode and the negative electrode; vi) an auxiliary oxygen gas recombination electrode electrically connected to the iron negative electrode by a first electronic component, ionically connected to the electrolyte by a first ionic pathway, and exposed to a gas headspace above the electrolyte level by a first gas pathway.

Abstract: In an aspect, provided is an alkaline rechargeable battery comprising: i) a battery container sealed against the release of gas up to at least a threshold gas pressure, ii) a volume of an aqueous alkaline electrolyte at least partially filling the container to an electrolyte level; iii) a positive electrode containing positive active material and at least partially submerged in the electrolyte; iv) an iron negative electrode at least partially submerged in the electrolyte, the iron negative electrode comprising iron active material; v) a separator at least partially submerged in the electrolyte provided between the positive electrode and the negative electrode; vi) an auxiliary oxygen gas recombination electrode electrically connected to the iron negative electrode by a first electronic component, ionically connected to the electrolyte by a first ionic pathway, and exposed to a gas headspace above the electrolyte level by a first gas pathway.

Abstract: According to one embodiment, a tissue penetrating device includes an elongate shaft having a proximal end, a distal end, and a lumen extending there between. A first needle is disposed within the lumen of the elongate shaft and is extendable therefrom between a first configuration and a second configuration. In the first configuration, the first needle is disposed within the elongate shaft's lumen and is substantially aligned with an axis of the lumen. In the second configuration, the first needle extends distally of the elongate shaft's distal end and bends away from the lumen's axis. A second needle is disposed within a lumen of the first needle and is extendable therefrom when the first needle is positioned in the first configuration and when the first needle is positioned in the second configuration. The second needle may be extended from the first needle to penetrate tissue of a patient.

Abstract: A system includes a data shuttle with rows of data storage devices, which are communicatively coupled to a shared printed circuit board assembly. Each row includes multiple data storage devices. The printed circuit board assembly is configured to communicatively couple to a first controller to enable storing data to the data storage devices and to communicatively coupled to a second controller to enable transferring data from the data storage devices.

Abstract: A heart tissue gripping device may include a body portion, an elongate shaft, and a tissue gripping member that is attached to the distal end of the elongate shaft. The tissue gripping member being may be positioned adjacent a heart surface by insertion through an incision in the body. The tissue gripping member may releasably attach to tissue of the heart surface to facilitate a surgical instrument in performing one or more procedures. A coupling of the tissue gripping member may releasably attach the surgical device to the tissue gripping member to allow the device to access the tissue of the heart surface.

Abstract: A system includes a data storage drive having a housing with one or more data storage media therein. The housing includes a top cover and a base-deck. The base-deck includes a floor and a frame having a plurality of sides. The data storage drive also includes a printed circuit board assembly (PCBA) mounted on an exterior of one of the plurality of sides of the frame.

Abstract: According to one embodiment, a protective device for use in congestive heart failure treatments, and other treatments, includes a control mechanism, an elongate shaft, and a protective plate. The control mechanism is coupled with a proximal end of the elongate shaft and the protective plate is pivotably coupled with a distal end of the elongate shaft. The elongate shaft enables the protective plate to be inserted within a body and navigated distally of a heart wall. The protective plate has a relatively wide and thin body portion and is pivotable relative to the elongate shaft by operation of the control mechanism. Pivoting and/or navigating of the protective plate within the body allows the protective plate to be positioned adjacent the heart wall to shield body organs or tissue surrounding the heart wall from being damaged by surgical instruments inserted through the heart wall.

Abstract: A system for treating a heart includes a catheter that is advanceable into a chamber of the heart and that is repositionable within the chamber between a septal wall and an external wall to enable penetration of the septal and external walls via a needle that is disposed within a lumen of the catheter. A first guidewire is deliverable through the penetration of the septal wall so that a distal end of the first guidewire is disposed within another chamber of the heart. A second guidewire is deliverable through the penetration of the external wall so that a distal end of the second guidewire is disposed externally of the external wall. The first guidewire is connectable to the second guidewire to join or form a path within the chamber that extends between the septal wall and the external wall.

Abstract: A device for bringing a target medium into contact with a carrier fluid comprises a chamber comprising a circumferential wall, a bottom wall and a top wall forming an enclosure for containing the target medium while contacting the carrier fluid, the chamber being substantially rotationally symmetric with respect to an axis of symmetry and adapted for remaining mechanically static in operation of the device. The device comprises a fluid inlet for injecting the carrier fluid into the chamber in a substantially tangential direction with respect to an inner surface of the circumferential wall, and an outlet. The device comprises a fluid distributor in the chamber for enabling the injected carrier fluid to pass through the distributor in a substantially inward radial direction, the distributor being substantially rotationally symmetric and adapted for rotating around the axis when driven by a transfer of momentum between the injected carrier fluid and the distributor.

Abstract: A method of determining a set of metrology point locations, the set including a subset of potential metrology point locations on a substrate, the method including: determining a relation between noise distributions associated with a plurality of the potential metrology point locations using existing knowledge; and using the determined relation and a model associated with the substrate to determine the set.

Abstract: A process for providing one or more thermoset polymeric materials onto an object is disclosed wherein said process comprises at least the following steps: Providing a polymeric composition having a viscosity >10 Pa.s at room temperature comprising at least one cross-linkable polymeric material; and then Optionally heating the polymeric composition to achieve a liquid cross-linkable polymeric composition having a viscosity below 4 Pa.

Abstract: A louvered panel assembly restricts the ingress of contaminants into an enclosure. The louvered panel assembly includes a first louvered panel, a second louvered panel, and a third louvered panel. The first louvered panel has a first plurality of louvers extending arcuately, downwardly, and outwardly from a first plate. The second louvered panel is coupled to the first louvered panel and has a second plurality of louvers extending arcuately, downwardly, and inwardly away from a second plate that is spaced apart from the first plate. The third louvered panel is coupled to the second louvered panel and has a third plurality of louvers extending arcuately, upwardly, and inwardly away from a third plate that is spaced apart from and extends approximately parallel to the second plate.

Abstract: A method for molding shaped silicone elastomeric articles from room temperature curable silicone compositions, which are practically not suited to being processed using extrusion techniques, is provided. The method enables the room temperature curable silicone composition to cure in a predefined shape (6) into which it is introduced to form a shaped silicone elastomeric article. The articles may be, for the sake of example, suitable for use as spacers for insulating glass units (IGUs).

Abstract: A method of determining a set of metrology point locations, the set including a subset of potential metrology point locations on a substrate, the method including: determining a relation between noise distributions associated with a plurality of the potential metrology point locations using existing knowledge; and using the determined relation and a model associated with the substrate to determine the set.

Abstract: A system includes a data shuttle with rows of data storage devices, which are communicatively coupled to a shared printed circuit board assembly. Each row includes multiple data storage devices. The printed circuit board assembly is configured to communicatively couple to a first controller to enable storing data to the data storage devices and to communicatively coupled to a second controller to enable transferring data from the data storage devices.

Abstract: Various fabrication method are disclosed. In one such method, at least one structure is formed on a substrate which protrudes outwardly from a plane of the substrate. A beam is used to form a layer of material, at least part of which is in direct contact with a semiconductor structure on the substrate, the semiconductor structure comprising at least one nanowire. The beam has a non-zero angle of incidence relative to the normal of the plane of the substrate such that the beam is incident on one side of the protruding structure, thereby preventing a portion of the nanowire in a shadow region adjacent the other side of the protruding structure in the plane of the substrate from being covered with the material.

Abstract: Various fabrication methods are disclosed. In one such method, at least one structure is formed on a substrate which protrudes outwardly from a plane of the substrate. A beam is used to form a layer of material, at least part of which is in direct contact with a semiconductor structure on the substrate, the semiconductor structure comprising at least one nanowire. The beam has a non-zero angle of incidence relative to the normal of the plane of the substrate such that the beam is incident on one side of the protruding structure, thereby preventing a portion of the nanowire in a shadow region adjacent the other side of the protruding structure in the plane of the substrate from being covered with the material.

Abstract: A method for performing a therapeutic intervention in a pericardial space of a heart includes delivering a catheter into a right atrium of the heart and steering the catheter so that a distal end of the catheter is positioned adjacent an access site in the right atrium. The distal end of the catheter is anchored in a heart wall of the right atrium adjacent the access site and the heart wall is inverted to separate an exterior surface of the inverted heart wall from contact with parietal pericardial tissue. The inverted heart wall is penetrated to provide access to the pericardial space around the heart. A device is delivered through the penetrating in the inverted heart wall to perform the therapeutic intervention in the pericardial space.

Abstract: A system includes a data storage drive having a housing with one or more data storage media therein. The housing includes a top cover and a base-deck. The base-deck includes a floor and a frame having a plurality of sides. The data storage drive also includes a printed circuit board assembly (PCBA) mounted on an exterior of one of the plurality of sides of the frame.

Abstract: Embodiments described herein include devices, systems, and methods for reducing the distance between two locations in tissue. In one embodiment, an anchor may reside within the right ventricle in engagement with the septum. A tension member may extend from that anchor through the septum and an exterior wall of the left ventricle to a second anchor disposed along a surface of the heart. Perforating the exterior wall and the septum from an epicardial approach can provide control over the reshaping of the ventricular chamber. Guiding deployment of the implant from along the epicardial access path and another access path into and through the right ventricle provides control over the movement of the anchor within the ventricle. The joined epicardial pathway and right atrial pathway allows the tension member to be advanced into the heart through the right atrium and pulled into engagement along the epicardial access path.