A system includes a downhole tool having a housing and a passage extending through the housing, where the passage includes an inlet configured to receive a flow of a wellbore fluid and an outlet configured to discharge the flow of the wellbore fluid. The downhole tool includes a heating element configured to heat the flow of the wellbore fluid and to enable the flow of the wellbore fluid to transition to a single-phase fluid flow within the passage. The downhole tool includes a phase composition sensor positioned adjacent the passage and configured to provide feedback indicative of formation of the single-phase fluid flow. The system includes a controller configured to monitor a power consumption of the heating element and to determine an enthalpy of the wellbore fluid based in part on the power consumption and the feedback from the phase composition sensor.

A testing apparatus includes a chamber. The chamber includes a holder configured to position a container. The chamber includes a first input device and a second input device, each partially outside the chamber and configured to: generate a first image of the container and generate a second image of the container. The chamber includes a first light source configured to illuminate the container for the first image. The chamber includes a second light source configured to illuminate the container for the second image.

The invention provides a system for observation of media dissolution and/or bacterial growth in a transparent bag, comprising a receptacle for supporting the bag, and a light emitting device arranged to transmit light into and/or through the interior of the bag supported at the receptacle. The media in the transparent bag can be visually inspected to confirm the dissolution state of the media and check for residual undissolved media and/or confirm the absence of unexpected microbial growth without having to move or handle the bag as it can remain supported in a defined orientation at the receptacle during repeated visual inspections by means of the light emitted from the light emitting device

A process for sizing two-dimensional nanostructures includes providing the nanostructures to a liquid-liquid interface, providing probe particles to the liquid-liquid interface, obtaining an image of the nanostructures and the probe particles, and processing the image to ascertain a size property of the nanostructures.

A device for measuring the state of a phase change material inside a vessel, the device includes at least one optical fiber arranged inside the vessel, the optical fiber including a cladding around a core, a light source emitting light coupled into a first end of the at least one optical fiber at a wavelength , optical measuring devices for measuring the amount of light at the output at a second end of the at least one optical fiber. The at least one optical fiber also includes a plurality of sections with the cladding removed so that at these sections the core is in direct contact with the phase change material inside the vessel and where the refractive index at the wavelength of the core is higher than that of the phase change material in a first phase and lower in a second phase.

A method of detecting free flocculant polymer having a net charge present in an aqueous phase of a multi-phase substance is provided. The multi-phase substance comprises a solid phase, an organic phase, and the aqueous phase. The method comprises separating the solid phase from the multi-phase substance to form a dual phase top liquid comprising the organic phase and the aqueous phase; separating the organic phase from the dual phase top liquid, leaving the aqueous phase; combining the free flocculant polymer in the aqueous phase and a dye having an opposite net charge than that of the free flocculant polymer, thereby causing a spectroscopically observable change in the aqueous phase; and analyzing the aqueous phase via spectrometry to determine the concentration of the free flocculant polymer in the multi-phase substance.

A micro-droplet fluorescence detection system, comprising a microfluidic chip (1), an optical path device, and a movement control device for controlling the chip (1) and an optical path device to move, so that the chip (1) moves relative to the optical path device during a fluorescence scanning detection process of micro-droplets in the chip (1), and the micro-droplets inside the chip (1) remains stationary relative to the chip (1). The micro-droplet fluorescence detection system has advantages of avoiding cross contamination due to closed detection, high detection rate, high throughput and high sensitivity.

Provided are methods and systems for efficiently and non-invasively identifying nuts (e.g., almonds) having concealed damage using near infrared scanning. The methods identify nuts having concealed damage with a certainty greater than 90% and an error rate that is less than 10%.

Certain implementations of the subject matter can be implemented as a method of screening demulsifiers for live crude oil-water emulsions. A live emulsion of a hydrocarbon sample and a water sample is flowed through a capillary viscometer. The live emulsion includes dissolved gases retrieved from a hydrocarbon-carrying reservoir. While flowing the live emulsion through the capillary viscometer, a demulsifier sample is flowed through the capillary viscometer. The demulsifier sample causes breakdown of the live emulsion. Using the capillary viscometer, change in a viscosity of the live emulsion over time resulting from the breakdown of the live emulsion due to the demulsifier sample is measured. Multiple images of the breakdown of the live emulsion over time are captured. A strength of the live emulsion is classified based, in part, on the change in the viscosity of the live emulsion over time and on the plurality of images.

Certain implementations of the subject matter can be implemented to screen demulsifiers. A live emulsion of a live hydrocarbon sample and a water sample is flowed through a capillary viscometer. The live hydrocarbon sample includes dissolved gases retrieved from a hydrocarbon-carrying reservoir. While flowing the live emulsion through the capillary viscometer, a demulsifier sample is flowed through the capillary viscometer. The demulsifier sample is capable of causing breakdown of the live emulsion. Using the capillary viscometer, change in a viscosity of the live emulsion over time resulting from the breakdown of the live emulsion due to the demulsifier sample is measured. Multiple images of the breakdown of the live emulsion over time are captured. A strength of the live emulsion is classified based, in part, on the change in the viscosity of the live emulsion over time and on the plurality of images.