There is provided a composition for topical application to the penis for the treatment of erectile dysfunction, the composition being free of glyceryl trinitrate (GTN), sildenafil and an acetylcholinesterase inhibitor, and comprising volatile and non-volatile solvents, the volatile solvents comprising a lower alcohol and water and the non-volatile solvents comprising a polyhydric alcohol and a glycol. Preferably, the composition does not contain any pharmaceutically active ingredients for the treatment of erectile dysfunction. Also provided is a method of determining the cooling ability of a test composition, such as the composition described above.

A sensor device for determining at least one heat transfer parameter of a gas comprises a sensor unit (10) comprising at least one heater element and at least one temperature sensor. A first (inner) housing (20) receives the sensor unit. The first housing comprises a first membrane (22) allowing a diffusive gas exchange between the exterior and the interior of the first housing. The first housing is received in a second (outer) housing (30). The second housing comprises a second membrane (32) allowing a diffusive gas exchange between the exterior of the second housing and the exterior of the first housing. Thereby temperature gradients inside the first housing are reduced. The second housing can be made of metal and can be disposed on a support plate (40), taking the form of a cap. An auxiliary sensor (50) can be arranged in the space between the first and second housings.

Ultrasensitive, ultrathin thermodynamic sensing platforms for the detection of chemical compounds at trace levels are disclosed. Embodiments of the ultrathin sensor comprise substrate, adhesion, microheater, and catalyst layers. A sensor array may include a plurality of sensors each having a different catalyst. When a sensor array exposed to an analyte, each of the various sensors of the array may experience an endothermic reaction, an exothermic reaction, or no reaction. A comparison of the reaction results to data comprising previously-obtained reaction results may be used to determine information on the analyte. Advantageously, these ultrathin vapor sensors utilize less power and provide greater sensitivity, and may be used to detect and identify analytes at the PPT level. Specialized sensors configured to detect analytes falling into a certain category (e.g., explosives, drugs and narcotics, biomarkers, etc.) are disclosed, as well as general purpose sensors capable of detecting analytes from a plurality of categories.

A fluid sensor for sensing a concentration or composition of a fluid, the sensor comprising: a semiconductor substrate comprising a first etched portion and a second etched portion; a dielectric region located on the semiconductor substrate, wherein the dielectric region comprises a first dielectric membrane located over the first etched portion of the semiconductor substrate, and a second dielectric membrane located over the second etched portion of the semiconductor substrate; two temperature sensing elements on or within the first dielectric membrane and two temperature sensing elements on or within the second dielectric membrane; an output circuit configured to measure a differential signal between the two temperature sensing elements of the first dielectric membrane and the two temperature sensing elements of the second dielectric membrane; wherein the first dielectric membrane is exposed to the fluid and the second dielectric membrane is isolated from the fluid.

The present disclosure provides a hydrogen peroxide sterilization sensor and method of use. The sensor includes: at least one thermal indicator component independently selected from an electronic thermal sensor, an irreversible temperature indicator, and a heat-shrinkable film; a reactant-functional porous sorbent in thermal contact (which may or may not be direct physical contact) with the at least one thermal indicator component; and a reactant comprising a material that reacts exothermically with hydrogen peroxide. The reactant is impregnated in the porous sorbent. The method includes: providing a hydrogen peroxide sterilization sensor; allowing hydrogen peroxide to contact the reactant to generate thermal energy sufficient to cause a response from the at least one thermal indicator component; and detecting that conditions for the hydrogen peroxide sterilization have been met.

The present disclosure provides an ammonia sensor and method of use. The sensor includes: at least one thermal indicator component independently selected from an electronic thermal sensor, an irreversible temperature indicator, and a heat-shrinkable film; an acid-functional porous sorbent in thermal contact with the at least one thermal indicator component; and an acid having a boiling point above 120° C. and a pKa of no greater than 2.5. The acid is impregnated in or covalently attached to the porous sorbent. The method includes: placing an ammonia sensor in contact with a container holding a volume of ammonia; and monitoring the ammonia sensor for a detectable response from the at least one thermal indicator component due to contact of ammonia with the acid that generates thermal energy sufficient to cause the response.

The present invention discloses a multi-screen supporting device in a high-temperature adiabatic calorimeter, and belongs to a calorimeter device in calorimetry. The multi-screen supporting device comprises a vacuum tank, three layers of protecting screens, two layers of thermal insulation screens, a protecting screen supporter for supporting and fixing the protecting screens, a thermal insulation screen supporter for supporting and fixing the thermal insulation screens, and a connecting piece for connecting and fixing the protecting screen supporter and the thermal insulation screen supporter. The multi-screen supporting mode in the high-temperature calorimeter solves the problems of time consumption for disassembling and assembling, low multi-screen assembling coaxiality and reduced experimental repeatability caused by many parts moved in each disassembling and assembling in the existing high-temperature calorimeter. The multi-screen supporting mode is easy in part processing, high in disassembling and assembling efficiency and convenient in operation, and effectively improves the experimental repeatability.

A system and method for high-throughput, high-resolution gas sorption screening are provided. An example system includes a sample chamber with a hermetic seal and a heat exchanger system. The heat exchanger system includes a heat exchanger disposed in the sample chamber, a coolant circulator fluidically coupled to the heat exchanger, and a sample plate comprising sample wells in contact with the cooling fluid from the coolant circulator. The system also includes a gas delivery system. The gas delivery system includes a gas source and a flow regulator. A temperature measurement system is configured to sense the temperature of the sample wells.

A differential scanning calorimetry sensor, comprises a substrate; a heater trace comprising a conductive material, on the substrate; an encapsulation layer, on the substrate and on the heater trace; and a sample heating area, which is on the heater trace. The heater trace has a thickness of 50 to 1000 nm, a width of 1 to 100 pm, and a path length of 5 to 500 mm. Also described are a sample holder, a sensor enclosure and a thermal analysis sensor system.

The present invention includes a method for thermodynamic formulation of a Langmuir isotherm comprising: (1), (1′) (1), (1′) where n.sub.i is the adsorption amount of gas component i; (1′) is the adsorption maximum amount; P is the gas vapor pressure, and K is the apparent adsorption equilibrium constant in which adsorption and desorption rates are proportional to a concentrations of vacant sites and occupied sites; and substituting the concentration of both a vacant site and an occupied site with site activities, wherein a reference state for the vacant sites is at zero surface coverage while the reference state for the occupied sites is at full surface coverage.

[00001]$\begin{array}{cc}\left(1^{\prime }\right)& \\ n_i=n_i^0\frac{\mathrm{KP}}{1+\mathrm{KP}}& \left(1\right)\end{array}$