A technique facilitates evaluation of a fluid, such as a fluid produced from a well. The technique utilizes a modular and mobile system for testing flows of fluid which may comprise mixtures of constituents, and for sampling fluids thereof. The multiphase sampling method includes flowing a multiphase fluid comprising an oil phase and a water phase through a first conduit, the oil phase and water phase at least partially separating in the first conduit, mixing together the oil phase and water phase to form a mixed bulk liquid phase by flowing the multiphase fluid through a flow mixer toward a second conduit downstream the flow mixer, sampling a portion of the mixed bulk liquid phase at location at or within the second conduit, wherein the sampled portion of the mixed bulk liquid phase has a water-to-liquid ratio (WLR) representative of the pre-mixed oil phase and water phase.

The present invention is directed to a method for the determination of the hyaluronic acid content of a hydrogel, the method comprising the following steps: a) preparing, as reagent A, a solution of sodium tetraborate in sulfuric acid; b) preparing reagent B by dissolving carbazole in ethanol; c) preparing test solutions by dissolving the hydrogel in an aqueous solution; d) treating the test solution with ultrasounds for a period of time sufficient to obtain a macroscopically homogeneous solution; e) preparing a reference stock solution by dissolving glucuronic acid, or a glucuronic acid-containing substance in an aqueous solution; f) preparing at least 3 reference solutions by dilution of the reference stock solution in aqueous solution, preferably at concentration comprised between 0.0005% w/v and 0.0100% w/v, preferably between 0.0010% w/v and 0.0050% w/v; g) preparing the test tubes by admixing reagent A, reagent B and one of the following: reference solution, test solution, aqueous solution (blank), and optionally solution for interference (crosslinker sample or additive sample); placing each test tube on a water bath for at least 5 min, then cool them to room temperature; h) reading the absorbance at a wavelength comprised between 500 and 580 nm, preferably at about 530 nm, against the blank and optionally the sample for interference.

The present invention is directed to a method for the determination of the hyaluronic acid content of a hydrogel, the method comprising the following steps: a) preparing, as reagent A, a solution of sodium tetraborate in sulfuric acid; b) preparing reagent B by dissolving carbazole in ethanol; c) preparing test solutions by dissolving the hydrogel in an aqueous solution; d) treating the test solution with ultrasounds for a period of time sufficient to obtain a macroscopically homogeneous solution; e) preparing a reference stock solution by dissolving glucuronic acid, or a glucuronic acid-containing substance in an aqueous solution; f) preparing at least 3 reference solutions by dilution of the reference stock solution in aqueous solution, preferably at concentration comprised between 0.0005% w/v and 0.0100% w/v, preferably between 0.0010% w/v and 0.0050% w/v; g) preparing the test tubes by admixing reagent A, reagent B and one of the following: reference solution, test solution, aqueous solution (blank), and optionally solution for interference (crosslinker sample or additive sample); placing each test tube on a water bath for at least 5 min, then cool them to room temperature; h) reading the absorbance at a wavelength comprised between 500 and 580 nm, preferably at about 530 nm, against the blank and optionally the sample for interference.

A field flow fractionator (FFF device) 1 classifies particles in a liquid sample by applying a field to a liquid sample supplied from a sample injection device 5. A detector 6 detects the particles in the liquid sample classified by the FFF device 1. A bypass flow path 8 supplies the liquid sample from the sample injection device 5 to the detector 6 without via the FFF device 1. A rotary valve (flow path switching unit) 4 switches a flow path to guide the liquid sample from the sample injection device 5 to the FFF device 1 or a bypass flow path 8. The bypass flow path 8 is provided with a concentration adjusting device 9 for adjusting the concentration of the liquid sample from the sample injection device 5. In a case where a sample with the same quantity as the sample supplied to the FFF device 1 is supplied to the bypass flow path 8 at the time of analysis, the sample is diluted by the concentration adjusting device 9 such that a detection signal from the detector 6 falls within a dynamic range.

A thin film induction nebulizer is disclosed herein. The nebulizer has a gas capillary and a liquid capillary that are aligned in the same direction within a nebulizer housing and are substantially aligned with a main axis of the nebulizer housing. The nebulizer includes a liquid opening configured to allow liquid to exit the liquid capillary and a gas orifice configured to allow gas to exit the gas capillary. The liquid capillary opens into a chamber that is formed from a liquid channel having a roughened surface and a cover plate. The cover plate interfaces with the liquid channel to partially seal the chamber. The chamber includes an opening where the liquid opening opens into the chamber and also includes another opening proximal to the gas orifice. The end of the nebulizer housing that is proximal to the liquid opening and the gas orifice includes two angled exterior surfaces.

A thin film induction nebulizer is disclosed herein. The nebulizer has a gas capillary and a liquid capillary that are aligned in the same direction within a nebulizer housing and are substantially aligned with a main axis of the nebulizer housing. The nebulizer includes a liquid opening configured to allow liquid to exit the liquid capillary and a gas orifice configured to allow gas to exit the gas capillary. The liquid capillary opens into a chamber that is formed from a liquid channel having a roughened surface and a cover plate. The cover plate interfaces with the liquid channel to partially seal the chamber. The chamber includes an opening where the liquid opening opens into the chamber and also includes another opening proximal to the gas orifice. The end of the nebulizer housing that is proximal to the liquid opening and the gas orifice includes two angled exterior surfaces.

A dosing module (137) in an agricultural environment, arranged to apply a milk sample of an animal (100) onto a dry stick (180a, 180b, 180c). The dosing module (137) includes a milk insertion connection (340) arranged to receive milk; a needle (350) configured to receive the milk and apply the received milk to the dry stick (180a, 180b, 180c); a first pump (611), configured to provide milk from the milk insertion connection (340) to the needle (350); and a position adjustment mechanism (510) configured to adjust the needle (350) between a retracted position (α) above the dry stick (180a, 180b, 180c) when dosing milk to the dry stick (180a, 180b, 180c), and at an extended position (β) when flushing milk through the needle (350); and an evacuator (195) arranged to intercept liquid output by the needle (350).

A dosing module (137) in an agricultural environment, arranged to apply a milk sample of an animal (100) onto a dry stick (180a, 180b, 180c). The dosing module (137) includes a milk insertion connection (340) arranged to receive milk; a needle (350) configured to receive the milk and apply the received milk to the dry stick (180a, 180b, 180c); a first pump (611), configured to provide milk from the milk insertion connection (340) to the needle (350); and a position adjustment mechanism (510) configured to adjust the needle (350) between a retracted position (α) above the dry stick (180a, 180b, 180c) when dosing milk to the dry stick (180a, 180b, 180c), and at an extended position (β) when flushing milk through the needle (350); and an evacuator (195) arranged to intercept liquid output by the needle (350).

A pressure cell for sum frequency generation spectroscopy includes: a metal pressure chamber; a heating stage that heats a liquid sample; an ultrasonic stage that emulsifies the liquid sample; a chamber pump that pressurizes an interior of the metal pressure chamber; and a controller that controls the chamber pump, the ultrasonic stage, and the heating stage to control a pressure of the interior of the metal pressure chamber, an emulsification of the liquid sample, and a temperature of the liquid sample, respectively. The metal pressure chamber includes: a liquid sample holder that retains the liquid sample; a removable lid that seals against a base; a window in the removable lid; a sample inlet that flows the liquid sample from an exterior of the metal pressure chamber to the liquid sample holder at a predetermined flow rate; and a sample outlet.

A pressure cell for sum frequency generation spectroscopy includes: a metal pressure chamber; a heating stage that heats a liquid sample; an ultrasonic stage that emulsifies the liquid sample; a chamber pump that pressurizes an interior of the metal pressure chamber; and a controller that controls the chamber pump, the ultrasonic stage, and the heating stage to control a pressure of the interior of the metal pressure chamber, an emulsification of the liquid sample, and a temperature of the liquid sample, respectively. The metal pressure chamber includes: a liquid sample holder that retains the liquid sample; a removable lid that seals against a base; a window in the removable lid; a sample inlet that flows the liquid sample from an exterior of the metal pressure chamber to the liquid sample holder at a predetermined flow rate; and a sample outlet.