The present invention provides an analytical method for precipitated particles during co-precipitation reaction, comprising: running a co-precipitation reaction in a reaction vessel to form a precipitated product; injecting a tracking metal to the reaction vessel for a given time duration; collecting the precipitated product containing the tracking metal from the reaction vessel in increments of time to obtain multiple product samples; filtering each collected product sample to separate precipitated particles from filtrate; performing elemental analysis for the tracking metal in the precipitated particles of each collected product sample, to obtain the residence time distribution of the precipitated particles in the reaction vessel according to the concentration of the tracking metal in the precipitated particles. By the analytical method, the preferred residence time of the precipitated particles in the reaction vessel can be ascertained, so that it is clear when the precipitated particles should be collected from the reaction vessel.

Method for detecting short-circuits in a coil in an electric machine, includes: a) arranging a coil in an air gap between the rotor and stator; c) recording signal curves generated by the coil; d) determining zero crossings of the curve and storing the times thereof; e) determining zero crossings of the curve corrected by an offset c, identifying a pair of immediately consecutive zero crossings, the time separation of which is longer than the minimum duration; f) in no pair is identified, repeating step e) until identified, wherein the offset c is varied from the zero point to a global extreme value of the curve; g) identifying at least one of the two stored times, which lies between and closest in time to the pair and; h) extracting two half-waves from the curve using times identified in step g), wherein each half-wave corresponds to half a revolution of the rotor.

A wet chemistry analyzer is provided. The wet chemistry analyzer comprises a reaction chamber configured to receive a reactant solution from a sample inlet and facilitate a process reaction. The wet chemistry analyzer also includes a detection chamber configured to receive a portion of a reaction mixture from the reaction chamber and measure a concentration of a chemical within the reaction mixture. The reaction chamber and the detection chamber are fluidically coupleable such that a portion of the reaction mixture can be directed to flow into the detection chamber to pre-condition a surface inside the detection chamber.

A wet chemistry analyzer is provided. The wet chemistry analyzer comprises a reaction chamber configured to receive a reactant solution from a sample inlet and facilitate a process reaction. The wet chemistry analyzer also includes a detection chamber configured to receive a portion of a reaction mixture from the reaction chamber and measure a concentration of a chemical within the reaction mixture. The reaction chamber and the detection chamber are fluidically coupleable such that a portion of the reaction mixture can be directed to flow into the detection chamber to pre-condition a surface inside the detection chamber.

Provided is an ion sensor including a supporting substrate, a plurality of cells, a silicon substrate, a plurality of transistors, and an analog-digital conversion circuit. The plurality of cells, the plurality of transistors, and the analog-digital conversion circuit are provided above the supporting substrate. Each of the plurality of transistors has a corresponding gate provided on a first surface of the silicon substrate. The analog-digital conversion circuit is provided on the silicon substrate. The ion-sensing surface is provided on a second surface of the silicon substrate. The second surface is opposite to the first surface.

The present invention comprises a method and device for the quantitative determination of levels of lead in paint. The device effectuates the completion of the method which involves selecting a measured sample of paint, vaporizing the paint sample, capturing the vaporized reaction products in a reaction vessel, and dissolving the resultant lead oxide into solution using aqueous acid, adding a titrated amount of a first chemical agent into the vessel capable of precipitating a desired quantity of lead from the solution, creating a color change. If there is an indication that lead is present, as measured by the color change, the operator adds a second chemical to the sample mixture, which reveals levels of lead which exceed the stoichiometric reaction with the first titrated reagent by a second color change. Thereby making a reliable, quantitive determination of lead content.

The present invention comprises a method and device for the quantitative determination of levels of lead in paint. The device effectuates the completion of the method which involves selecting a measured sample of paint, vaporizing the paint sample, capturing the vaporized reaction products in a reaction vessel, and dissolving the resultant lead oxide into solution using aqueous acid, adding a titrated amount of a first chemical agent into the vessel capable of precipitating a desired quantity of lead from the solution, creating a color change. If there is an indication that lead is present, as measured by the color change, the operator adds a second chemical to the sample mixture, which reveals levels of lead which exceed the stoichiometric reaction with the first titrated reagent by a second color change. Thereby making a reliable, quantitive determination of lead content.

A benchtop device flow setup for determining the effectiveness of magnetic treatment of feed water for reducing mineral scaling includes two similar branches, both equipped with a reverse osmosis membrane and a pump that operate in the transient regime at the same flow rate and transmembrane pressure. The flow setup is further fed with a solution at the same level of supersaturation measured in a stirred reactor, however, only one branch exposes the feed to a magnetic field.

A benchtop device flow setup for determining the effectiveness of magnetic treatment of feed water for reducing mineral scaling includes two similar branches, both equipped with a reverse osmosis membrane and a pump that operate in the transient regime at the same flow rate and transmembrane pressure. The flow setup is further fed with a solution at the same level of supersaturation measured in a stirred reactor, however, only one branch exposes the feed to a magnetic field.

A method for determining the asphaltene content of oil includes obtaining an oil sample, determining an optical spectrum of the oil sample and removing asphaltenes from the oil sample by precipitating asphaltenes using a first alkane precipitant. The method also includes determining an optical spectrum of maltenes of the oil sample and subtracting the optical spectrum of the maltenes of the oil sample from the optical spectrum of the oil sample to yield an optical spectrum of asphaltenes of the oil sample. The method further includes using the optical spectrum of asphaltenes of the oil sample to determine asphaltene content of the oil sample using a second alkane precipitant.