Abstract: A motion conversion device is disclosed for converting motion in one direction into motion in another direction. The motion conversion device may include a single-acting cylinder hydraulically or pneumatically coupled to a double-acting cylinder such that movement of the single-acting cylinder along an axis causes movement of the double-acting cylinder along a non-parallel axis. The single-acting cylinder may be mechanically coupled to another single-acting cylinder such that movement of one of the single-acting cylinders in a direction causes movement of the other one of the single-acting cylinders in an opposite direction. In this way, the single-acting cylinders may cooperate to provide reciprocal motion of the double-acting cylinder. Also disclosed is a valve incorporating a motion conversion device for the purpose of moving a closure member between an open position and a closed position. Furthermore, a method for operating a valve closure member with a motion conversion device is disclosed.

Abstract: A method for controlling the operation of a vehicle prime mover based on the engagement status of one or more safety restraints of the vehicle. In various implementations the method comprises monitoring, via a RPM controller of the vehicle, an operational status of vehicle, monitoring, via the RPM controller, the engagement status at least one passenger safety restraint of the vehicle, and limiting, via the RPM controller, a rotational speed, e.g., revolutions per minute (RPM) of one or more prime mover of the vehicle when the vehicle is in a On operational status and the at least one safety restraint is in a disengaged status.

Abstract: A water-soluble unit dose article including a water-soluble film and at least a first internal compartment, where the internal compartment includes one or more of a first particle, where the first particle includes between about 45% and about 95% by weight of the first particle of a water-soluble carrier material selected from inorganic alkali metal salts, organic alkali metal salts, inorganic alkaline earth metal salts, organic alkaline earth metal salts, organic acids, carbohydrates, silicates, urea, and mixtures thereof; between about 1% and about 50% by weight of the first particle of a benefit agent; and less than about 20% by weight of the first particle of a surfactant.

Abstract: A water-soluble unit dose article that includes a water-soluble film and at least a first internal compartment, where the first internal compartment includes one or more of a first particle, where the first particle comprises between about 45% and about 95% by weight of the first particle of a carrier material selected from polyethylene glycol, polyvinyl alcohol, urea, polyurethane, silica, alkoxylated fatty alcohols or mixtures thereof, between about 1% and about 50% by weight of the first particle of a benefit agent, and less than about 20% by weight of the first particle of a surfactant.

Abstract: A motion conversion device is disclosed for converting motion in one direction into motion in another direction. The motion conversion device may include a single-acting cylinder hydraulically or pneumatically coupled to a double-acting cylinder such that movement of the single-acting cylinder along an axis causes movement of the double-acting cylinder along a non-parallel axis. The single-acting cylinder may be mechanically coupled to another single-acting cylinder such that movement of one of the single-acting cylinders in a direction causes movement of the other one of the single-acting cylinders in an opposite direction. In this way, the single-acting cylinders may cooperate to provide reciprocal motion of the double-acting cylinder. Also disclosed is a valve incorporating a motion conversion device for the purpose of moving a closure member between an open position and a closed position. Furthermore, a method for operating a valve closure member with a motion conversion device is disclosed.

Abstract: A magnetically driven micropump for handling small fluid volumes. The micropump includes a first chamber and a second chamber. A flexible membrane being disposed between the first and second chambers. The flexible membrane being magnetically coupled to an actuator for displacing the membrane.

Abstract: A defibrillator system optimizes the timing and manner of applying a defibrillator charge to a patient based upon data provided to the defibrillator from a utility module or one or more external devices. A parameter module on the utility module provides the defibrillator with patient parameter information. Devices external to the utility module may provide the utility module with coaching data that the utility module may pass through to the defibrillator as a proxy to the external devices. The utility module may also provide external devices with patient data that the utility module may pass through to the external devices as a proxy to the defibrillator on a scheduled or other basis. The utility module may additionally provide a reserve of power to enable defibrillators to be used where power is unavailable and to enable defibrillators to deliver multiple charges more readily anywhere, anytime.

Abstract: A magnetically driven micropump for handling small fluid volumes. The micropump includes a first chamber and a second chamber. A flexible membrane being disposed between the first and second chambers. The flexible membrane being magnetically coupled to an actuator for displacing the membrane.

Abstract: Provided are systems and methods using which users may learn and become familiar with the effects of various aspects of their lifestyle on their health, e.g., users may learn about how food and/or exercise affects their glucose level and other physiological parameters, as well as overall health. In some cases the user selects a program to try; in other cases, a computing environment embodying the system suggests programs to try, including on the basis of pattern recognition, i.e., by the computing environment determining how a user could improve a detected pattern in some way. In this way, users such as type II diabetics or even users who are only prediabetic or non-diabetic may learn healthy habits to benefit their health.

Abstract: Provided are systems and methods using which users may learn and become familiar with the effects of various aspects of their lifestyle on their health, e.g., users may learn about how food and/or exercise affects their glucose level and other physiological parameters, as well as overall health. In some cases the user selects a program to try; in other cases, a computing environment embodying the system suggests programs to try, including on the basis of pattern recognition, i.e., by the computing environment determining how a user could improve a detected pattern in some way. In this way, users such as type II diabetics or even users who are only prediabetic or non-diabetic may learn healthy habits to benefit their health.

Abstract: Provided are systems and methods using which users may learn and become familiar with the effects of various aspects of their lifestyle on their health, e.g., users may learn about how food and/or exercise affects their glucose level and other physiological parameters, as well as overall health. In some cases the user selects a program to try; in other cases, a computing environment embodying the system suggests programs to try, including on the basis of pattern recognition, i.e., by the computing environment determining how a user could improve a detected pattern in some way. In this way, users such as type II diabetics or even users who are only prediabetic or non-diabetic may learn healthy habits to benefit their health.

Abstract: A consumer product composition comprises a non-porous dissolvable solid structure comprising a carrier material and a hydrophobic conditioning agent disposed within the carrier material, wherein the hydrophobic conditioning agent has a mean particle size of from about 2 ?m to about 2000 ?m.

Abstract: A consumer product composition comprises a non-porous dissolvable solid structure comprising from about 30% to about 95%, by weight of the consumer product composition, of a carrier material, and from about 5% to about 50%, by weight of the consumer product composition, of a hydrophobic conditioning agent disposed within the carrier material of the non-porous dissolvable solid structure. The carrier material comprises a polyethylene glycol material, or mixtures thereof, having a molecular weight of from about 200 to about 50,000. The hydrophobic conditioning agent is selected from the group consisting of silicone materials, organic conditioning oils, hydrocarbon oils, fatty esters, metathesized unsaturated polyol esters, silane-modified oils, and mixtures thereof.

Abstract: A process of making a consumer product composition comprising a non-porous dissolvable solid structure comprises the steps of: providing a carrier material having a melting point of greater than 25° C.; heating the carrier material to a temperature greater than the melting point of the carrier material to form liquefied carrier material; mixing a hydrophobic conditioning agent with the liquefied carrier material to form a melt composition; and cooling the melt composition to a temperature below the melting point of the carrier material to form the non-porous dissolvable solid structure of the consumer product composition. The carrier material and hydrophobic conditioning agent are selected to provide a Modified Capillary Number of less than about 10 with respect to the melt composition of the process.

Abstract: A medical device for caring for a patient includes a patient utility for measuring a patient parameter or administering a therapy to the patient and an alarm system that has a receiver to accept status information about the medical device. A use detector of the alarm system is structured to determine when the medical device is being prepared for use and a status detector of the alarm system is adapted to determine from the status information that the medical device is in a ready state. The alarm system further includes an alarm that is activated when the medical device is both being prepared for use and not in the ready state. This description also includes methods of generating an alarm when the medical device is both being prepared for use and not in the ready state.

Abstract: A consumer product composition comprises a non-porous dissolvable solid structure comprising a carrier material and a hydrophobic conditioning agent disposed within the carrier material, wherein the hydrophobic conditioning agent has a viscosity at 25° C. of at least about 0.01 Pa·s.

Abstract: A consumer product composition comprises a non-porous dissolvable solid structure comprising a carrier material and at least about 5%, by weight of said consumer product composition, of a hydrophobic conditioning agent disposed within said carrier material.

Abstract: A consumer product composition comprises a non-porous dissolvable solid structure comprising a carrier material having a viscosity at 70° C., and a hydrophobic conditioning agent having a viscosity at 70° C. The hydrophobic conditioning agent is disposed within the carrier material of the non-porous dissolvable solid structure. A ratio of the viscosity of the hydrophobic conditioning agent at 70° C. to the viscosity of the carrier material at 70° C. is from about 1000:1 to about 1:1000.

Abstract: A defibrillator system optimizes the timing and manner of applying a defibrillator charge to a patient based upon data provided to the defibrillator from a utility module or one or more external devices. A parameter module on the utility module provides the defibrillator with patient parameter information. Devices external to the utility module may provide the utility module with coaching data that the utility module may pass through to the defibrillator as a proxy to the external devices. The utility module may also provide external devices with patient data that the utility module may pass through to the external devices as a proxy to the defibrillator on a scheduled or other basis. The utility module may additionally provide a reserve of power to enable defibrillators to be used where power is unavailable and to enable defibrillators to deliver multiple charges more readily anywhere, anytime.

Abstract: A defibrillator system optimizes the timing and manner of applying a defibrillator charge to a patient based upon data provided to the defibrillator from a utility module or one or more external devices. A parameter module on the utility module provides the defibrillator with patient parameter information. Devices external to the utility module may provide the utility module with coaching data that the utility module may pass through to the defibrillator as a proxy to the external devices. The utility module may also provide external devices with patient data that the utility module may pass through to the external devices as a proxy to the defibrillator on a scheduled or other basis. The utility module may additionally provide a reserve of power to enable defibrillators to be used where power is unavailable and to enable defibrillators to deliver multiple charges more readily anywhere, anytime.