The electron capture detector (100) is a device for detecting a sample (?1). The electron capture detector (100) includes a detection cell (1), a sample inlet (2), and an electron emitting element (20). The detection cell (1) forms a reaction chamber (6). The sample inlet (2) introduces a first carrier gas containing the sample (?1) into the reaction chamber (6). The electron emitting element (20) emits electrons (?) into the reaction chamber (6). An ion (?2) derived from the sample component is generated as a result of the electron emitting element (20) emitting electrons (?) into the reaction chamber (6).

The present invention relates to method and an apparatus for quantitatively analyzing a gaseous process stream, in particular a stream from a process for producing ethylene carbonate and/or ethylene glycol, in particular where such stream comprises gaseous organic iodides.

The present invention relates to method and an apparatus for quantitatively analyzing a gaseous process stream, in particular a stream from a process for producing ethylene carbonate and/or ethylene glycol, in particular where such stream comprises gaseous organic iodides.

The present invention relates to biomarkers associated with multiple sclerosis (MS), particular GLX molecules, and teven more particular GLX-related glycosaminoglycans (GAGs) and GLX-related proteoglycans (PGs).

The present disclosure provides compositions, methods, and systems for identifying marked hydrocarbon fluids. These compositions, methods, and systems utilize a gas chromatography marker including a non-pyrrolidinone nitrogen-containing compound. The methods and systems can identify the presence or absence of the gas chromatography marker and/or the non-pyrrolidinone nitrogen-containing compound. The compositions, methods, and systems can optionally utilize a spectroscopic marker.

The present disclosure provides compositions, methods, and systems for identifying marked hydrocarbon fluids. These compositions, methods, and systems utilize a gas chromatography marker including a non-pyrrolidinone nitrogen-containing compound. The methods and systems can identify the presence or absence of the gas chromatography marker and/or the non-pyrrolidinone nitrogen-containing compound. The compositions, methods, and systems can optionally utilize a spectroscopic marker.

A method for process monitoring and control of a chemical reactor in which a chemical reaction utilizing a halogenated selectivity modifier is performed includes: measuring a level of halogenated components in an inlet stream of a reactor inlet; measuring a level of halogenated components in an outlet stream of a reactor outlet; based on the level of halogenated components at the inlet stream and the outlet stream, determining a process performance indicator associated with a halogenated component; and adjusting an amount of halogenated selectivity modifier added to the reactor based on the process performance indicator.

A method for process monitoring and control of a chemical reactor in which a chemical reaction utilizing a halogenated selectivity modifier is performed includes: measuring a level of halogenated components in an inlet stream of a reactor inlet; measuring a level of halogenated components in an outlet stream of a reactor outlet; based on the level of halogenated components at the inlet stream and the outlet stream, determining a process performance indicator associated with a halogenated component; and adjusting an amount of halogenated selectivity modifier added to the reactor based on the process performance indicator.

Disclosed is a microfluidic chip, including a chip upper cover, a chip lower layer, a membrane, a sealing gasket and a sealing ring. The microfluidic chip is provided with a sample storage zone, a droplet formation zone, a droplet storage zone, a droplet detection zone and a waste liquid storage zone. The sample storage zone, the droplet formation zone, the droplet storage zone, the droplet detection zone and the waste liquid storage zone communicate by means of a micropore or a micro-channel. The droplet formation zone is used to transform the sample phase into tens of thousands to millions of droplets, the droplets undergo the PCR reaction in the droplet storage zone, the droplet detection zone is used to perform optical detection on the droplets after PCR reaction, and the waste liquid storage zone is used to collect and store the detected droplets and continuous phase.

Provided is an automatic analysis device that can suppress concentration of a reagent made to react with a specimen. This automatic analysis device is provided with: a reagent container which accommodates a reagent and which has attached thereto a perforable lid; a perforation unit for perforating the lid; and a reagent suction nozzle that is inserted into a hole formed by perforation and that sucks up the reagent. The automatic analysis device is characterized by being further provided with a state storage unit that stores the state as to whether the reagent container is in an unused state or in a used state, and a state update unit that, when the lid is perforated by the perforation unit while the reagent container is in an unused state, updates the state stored in the state storage unit to the used state.