To sample cooling water from a discharge pipe under vacuum, with a simple structure and without using a large-scale device. Provided is a sampling system for sampling cooling water flowing through a discharge pipe extending from a condenser to a sea. The sampling system includes: a bypass pipe branched off from the discharge pipe and joining the discharge pipe; two shutoff valves provided in the bypass pipe; a sampling pipe branched off from the bypass pipe between the two shutoff valves; a vent pipe branched off from the bypass pipe between the two shutoff valves; a sampling valve provided in the sampling pipe; and a vent valve provided in the vent pipe.

Various implementations include a device for analyzing total organic carbon (TOC) within a fluid. The device includes a primary container, an input conduit, and an output conduit. The primary container is hollow and has a primary side wall and a primary end wall. The primary side wall has an inner surface defining a primary cavity and an outer surface opposite and spaced apart from the inner surface. The primary end wall includes a septum that is resiliently penetrable by an analyzer needle of a grab analysis port of a TOC analyzer. The input conduit has an input lumen. The input conduit extends through the primary container such that the input lumen is in fluid communication with the primary cavity. The output conduit has an output lumen.

Methods and apparatuses for fluid sensing system are disclosed. The method can include providing a first portion of a sample fluid in a sensing channel, holding the first portion of the sample fluid in the sensing channel for a first diffusion period, after the first diffusion period, providing a second portion of the sample fluid in the sensing channel, holding the second portion of the sample fluid in the sensing channel for a second diffusion period, and after the second diffusion period, sensing the second portion of the sample fluid in the sensing channel by a sensing element. Providing pulses of sample with intervening diffusion periods can produce more uniform analyte concentration across sensors with less overall volume of sample fluid.

Some embodiments described herein relate to a method that includes separating an analyte-containing sample via electrophoresis in a capillary. The capillary is loaded with a chemiluminescence agent, such as luminol, that is configured to react with the analyte (e.g., HRP-conjugated proteins) to produce a signal indicative of a concentration and/or quantity of analyte at each location along the length of the capillary. A first image of the capillary containing the analytes and the chemiluminescence agent is captured over a first period of time. A second image of the capillary containing the analytes and the chemiluminescence agent is captured over a second, longer, period of time. A concentration and/or quantity of a first population of analytes at a first location is determined using the first image, and a concentration and/or quantity of a second population of analytes at a second location is determined using the second image.

Some embodiments described herein relate to a method that includes separating an analyte-containing sample via electrophoresis in a capillary. The capillary is loaded with a chemiluminescence agent, such as luminol, that is configured to react with the analyte (e.g., HRP-conjugated proteins) to produce a signal indicative of a concentration and/or quantity of analyte at each location along the length of the capillary. A first image of the capillary containing the analytes and the chemiluminescence agent is captured over a first period of time. A second image of the capillary containing the analytes and the chemiluminescence agent is captured over a second, longer, period of time. A concentration and/or quantity of a first population of analytes at a first location is determined using the first image, and a concentration and/or quantity of a second population of analytes at a second location is determined using the second image.

An automated computer-controlled sampling system and related methods for collecting, processing, and analyzing agricultural samples for various chemical properties such as plant available nutrients. The sampling system allows multiple samples to be processed and analyzed for different analytes or chemical properties in a simultaneous concurrent or semi-concurrent manner. Advantageously, the system can process soil samples in the “as collected” condition without drying or grinding. The system generally includes a sample preparation sub-system which receives soil samples collected by a probe collection sub-system and produces a slurry (i.e. mixture of soil, vegetation, and/or manure and water), and a chemical analysis sub-system which processes the prepared slurry samples for quantifying multiple analytes and/or chemical properties of the sample. The sample preparation and chemical analysis sub-systems can be used to analyze soil, vegetation, and/or manure samples. A soil collection system is disclosed which captures and directs samples to the sampling system for processing.

The present invention relates to a microfluidic particle analysis device comprising an inlet in fluid communication via a main channel defining a main flow direction with an inlet manifold providing parallel fluid communication with a bypass channel of hydrodynamic resistance R.sub.bypass, and a measuring channel of hydrodynamic resistance R.sub.measuring, the measuring channel having a cross-sectional dimension in the range of from 1 μm to 50 μm and further having a sensor system for detecting a particle, wherein a flow distribution parameter X.sub.measuring=R.sub.measuring.sup.−1(R.sub.measuring.sup.−1+R.sub.bypass.sup.−1).sup.−1 is in the range from 10.sup.−6 to 0.25, wherein the angle of the measuring channel relative to the main flow direction is in the range of 0° to 60°, and wherein the angle of the bypass channel relative to the main flow direction is in the range of 0° to 60°, and the microfluidic particle analysis device further comprising an outlet in fluid communication with the bypass channel and the measuring channel. The present invention relates to a method of using the device microfluidic particle analysis.

In a centrifugal scroll screen apparatus there is provided a scroll assembly (20) driven by a scroll assembly drive shaft (25) and being connected to the scroll assembly by an axial adjuster comprising a shaft cam portion (92) and a scroll portion (96) each having a respective camming surface (94) whereby relative rotation of the scroll portion (96) and the shaft portion (92) axially adjusts the proximity of the vanes to a coaxial conical screening surface, and a locking ring (97) selectively operable to rotationally secure the scroll portion (96) and the shaft portion (92).

In a centrifugal scroll screen apparatus there is provided a scroll assembly (20) driven by a scroll assembly drive shaft (25) and being connected to the scroll assembly by an axial adjuster comprising a shaft cam portion (92) and a scroll portion (96) each having a respective camming surface (94) whereby relative rotation of the scroll portion (96) and the shaft portion (92) axially adjusts the proximity of the vanes to a coaxial conical screening surface, and a locking ring (97) selectively operable to rotationally secure the scroll portion (96) and the shaft portion (92).

In a centrifugal screening apparatus wherein a housing (10, 11) mounts a screen assembly (12) and a scroll assembly (20) to be differentially rotated about the machine axis, there is provided an inlet assembly (30) having an inlet body (31) defining an annular inlet space (32) coaxial with and opening in to an open apical end of the screen assembly (12) and a material supply conduit (35) delivering material to be screened to the annular space (32) and being aligned in a tangent to the annular space to deliver material to the screen assembly (12) substantially in the direction of rotation of the screen assembly (12).