A method for analysing a crude oil to determine the amount of organic acid compounds contained in the crude oil includes extracting the organic acid compounds from a sample of crude oil to form an extract and determining the amount of the extracted organic acids In addition, the method includes dissolving the extract in a polar solvent to form a solution of the extracted organic acid compounds Further, the method includes introducing a sample of the solution of the extracted organic acid to an apparatus including a reversed phase liquid chromatography (LC) column and a mass spectrometer (MS) arranged in series. The reversed phase LC column contains a hydrophobic sorbent and the mobile phase for the LC column includes a polar organic solvent. Still further, the method includes separating the organic acid compounds in the LC column of the LC-MS apparatus and continuously passing the separated organic acid compounds from the LC column to the MS of the LC-MS apparatus to ionize the organic acid compounds and to obtain a chromatogram with mass spectral data over time for the ionized organic acid compounds. Moreover, the method includes determining the area(s) under the peak(s) in an extracted ion chromatogram derived from the mass spectral data assigned to one or more organic acid compounds. The method also includes determining the amount of the organic acid compound(s) in the sample by comparing the area under the peak(s) assigned to the organic acid compound(s) with the area under a peak in an extracted ion chromatogram assigned to a specific amount of a standard organic acid compound. In addition, the method includes extrapolating from the amount of the organic acid compound(s) in the sample to provide the total amount of the organic acid compound(s) in the extract.

The invention generally relates to methods of analyzing crude oil. In certain embodiments, methods of the invention involve obtaining a crude oil sample, and subjecting the crude oil sample to mass spectrometry analysis. In certain embodiments, the method is performed without any sample pre-purification steps.

Provided is a method for introducing into a probe 22 an eluate eluted from a component separation unit 14 that temporally separates components contained in a liquid sample, for obtaining charged particles, and for delivering the charged particles to a charged particle analysis unit 30 provided at a subsequent stage through a charged particle introduction opening 23, comprising steps of: supplying a gasification promoting gas for promoting gasification of the eluate and applying a predetermined charged-particle obtaining voltage to the probe 22 while the eluate is being introduced into the probe 22; and hindering the eluate nebulized by the probe 22 from moving toward the ion introduction opening 2 only in a time period other than a time period in which a target-component containing eluate is introduced into the probe 22.

An accommodation unit includes a plurality of accommodation positions, each of the plurality of accommodation positions being capable of accommodating one of the plurality of samples. A detection unit detects identification information of each of the plurality of samples in the accommodation unit. A control unit holds the identification information of each of the plurality of samples received from the detection unit as detected identification information. The control unit is configured to receive identification information of each of a plurality of samples designated as analysis targets, and hold the received identification information as designated identification information. The control unit includes a notification means configured to output a warning before analysis is started by the analysis unit, when the control unit makes a comparison between the designated identification information and the detected identification information and determines that there is a mismatch therebetween.

A spray area in which a large number of droplets of a liquid sample sprayed from a spray nozzle (3) is separated from the tip of a needle electrode (14) for corona discharge by a sufficiently large distance, with a grid electrode (15) facing the needle electrode (14) placed in between. Ring electrodes (16) for creating an electric field which drives primary ions that should react with the sample and generate sample-derived ions are provided within an ion chamber (10) between the grid electrode (15) and the spray area. Primary ions generated by corona discharge within the space between the needle electrode (14) and the grid electrode (15) pass through the opening of the grid electrode (15), reach the spray area under the effect of the electric field, and ionize sample components. Since the droplets are prevented from adhering to the needle electrode (14), the corona discharge is maintained in a stable state. The resultant primary ions are efficiently transported and used for the ionization of the sample. Therefore, no spike noise due to an unstable corona discharge occurs, so that a high-quality spectrum can be obtained.

An apparatus is disclosed comprising a first device for generating aerosol, smoke or vapour from one or more regions of a target, an inlet conduit to an ion analyser or mass spectrometer, the inlet conduit having an inlet through which the aerosol, smoke or vapour passes, and a Venturi pump arrangement arranged and adapted to direct the aerosol, smoke or vapour towards the inlet.

The invention generally relates to methods of analyzing crude oil. In certain embodiments, methods of the invention involve obtaining a crude oil sample, and subjecting the crude oil sample to mass spectrometry analysis. In certain embodiments, the method is performed without any sample pre-purification steps.

An apparatus for mass spectrometry and/or ion mobility spectrometry is disclosed comprising a first device arranged and adapted to generate aerosol, smoke or vapour from a target and one or more second devices arranged and adapted to aspirate aerosol, smoke, vapour and/or liquid to or towards an analyser. A liquid trap or separator is provided to capture and/or discard liquid aspirated by the one or more second devices.

A liquid sample analyzing system including an ion analyzer having a first ion source receiving a target sample and a second ion source receiving a reference sample; a liquid sample introduction mechanism 3 including a passage-switching section introducing reference samples into the second ion source; and a controller for repeatedly performing a series of steps in the ion analyzer, the steps including: a pre-measurement step for initiating a measurement; a measurement step for introducing a target sample into the first ion source and performing a measurement on an ion originating from the target sample along with an ion originating from a reference sample introduced into the second ion source by the liquid sample introduction mechanism; and a post-measurement step where the liquid sample introduction mechanism operates concurrently with the predetermined post-measurement step to switch the passage-switching section to a passage having a reference sample for the next analysis.

A spray area in which a large number of droplets of a liquid sample sprayed from a spray nozzle is separated from the tip of a needle electrode for corona discharge by a sufficiently large distance, with a grid electrode facing the needle electrode placed in between. Ring electrodes for creating an electric field which drives primary ions that should react with the sample and generate sample-derived ions are provided within an ion chamber between the grid electrode and the spray area. Primary ions generated by corona discharge within the space between the needle electrode and the grid electrode pass through the opening of the grid electrode, reach the spray area under the effect of the electric field, and ionize sample components. Since the droplets are prevented from adhering to the needle electrode, the corona discharge is maintained in a stable state.