The present invention is in relation to a method and its apparatus, by means of which HCl generation formed from hydrolysis reactions or thermal decomposition of chloride salts is continuously monitored. Its application is in oil refining or in any other area where chloride salts are heated to temperatures high enough to cause hydrolysis reactions or thermal decomposition. The invention allows for a much more sophisticated and precise record of the thermal events that occur as a function of temperature. It also allows the behavior of chloride salts subjected to these conditions to be evaluated, both in model systems and in industrial saline solutions, with respect to the respective content, composition, or presence of components in the oil phase, such as carboxylic (naphthenic acids) or nitrogenous (ammonia or amines) acids.

A dual balance electrode trap having an outer chamber, a droplet dispenser holder removably coupled to the top surface of the outer chamber, and a rod holder having a central opening and four peripheral openings that are sized and shaped to allow four respective quadrupole metal rods to pass therethrough. The droplet dispenser holder has a top surface, a bottom surface, and a through hole that extends from the dispenser holder top surface to the droplet dispenser bottom surface. The through hole has a larger diameter portion adjacent to the top surface and a smaller diameter portion adjacent to the bottom surface, thereby preventing a droplet dispenser distal tip from extending entirely through the hole and contacting electrodes in the DBET. The rod holder is configured to be removably coupled to the quadrupole metal rods so that a location of the rod holder relative to the metal rods is adjustable.

Some embodiments of a blood coagulation testing system include an analyzer console device and a single-use cartridge component configured to releasably install into the console device. In some embodiments, the blood coagulation testing system can operate as an automated thromboelastometry system that is particularly useful, for example, at a point-of-care site.

A sampling needle is provided for piercing a septum of a vial containing a sample and aspirating the sample from the vial. The needle may include: a tubular core having a lumen extending therethrough and a piercing end, wherein the tubular core is formed of a bioinert material; a hollow support encircling the tubular core with the piercing end extending outwardly from the support, wherein the support is formed of a rigid material; and a bioinert coating covering a portion of the support adjacent the piercing end, wherein the tubular core and the covering isolates the support from the sample.

The method includes preparing a liquid supply pipe in which the solution to be inspected, air, and oil are disposed in this order, and installing the liquid supply pipe above the substrate at an angle such that the solution to be inspected is positioned on a lowermost side and the solution to be inspected, the air, and the oil flow onto a front surface of the substrate by gravity. A cross-sectional area of the liquid supply pipe is designed such that the air continues to be present between the solution to be inspected and the oil while the solution to be inspected, the air, and the oil are flowing through the liquid supply pipe, and after the solution to be inspected is supplied to the spot, the solution to be inspected present on the front surface of the substrate is replaced with the air, and then the liquid supply progresses.

Provided herein, among other aspects, are methods and apparatuses for analyzing particles in a sample. In some aspects, the particles can be analytes, cells, nucleic acids, or proteins and contacted with a tag, partitioned into aliquots, detected by a ranking device, and isolated. The methods and apparatuses provided herein may include a microfluidic chip. In some aspects, the methods and apparatuses may be used to quantify rare particles in a sample, such as cancer cells and other rare cells for disease diagnosis, prognosis, or treatment.

Provided herein, among other aspects, are methods and apparatuses for analyzing particles in a sample. In some aspects, the particles can be analytes, cells, nucleic acids, or proteins and contacted with a tag, partitioned into aliquots, detected by a ranking device, and isolated. The methods and apparatuses provided herein may include a microfluidic chip. In some aspects, the methods and apparatuses may be used to quantify rare particles in a sample, such as cancer cells and other rare cells for disease diagnosis, prognosis, or treatment.

The present invention relates to a bioprocess bag 118 comprising a bag wall defining an enclosed volume for holding biomaterials. The bag wall comprises at least one inlet port 142 and at least one outlet port 146. The bioprocess bag 118 also comprises a tube structure 400 comprising a first opened-end proximate the bag wall and a second distal end, the tube extending into the enclosed volume, and the tube structure 400 comprising a reinforced portion 402 proximate the first opened-end.

A microfluidic analysis device and manufacturing method are provided. The microfluidic analysis device includes a capillary substrate, a cover substrate adjacent to a cover side of the capillary substrate and/or a bottom substrate adjacent to a bottom side of the capillary substrate, a capillary structure with at least one capillary, forming a hollow channel, in the interior of the capillary substrate and/or at the interface of the capillary substrate with the cover substrate and/or at the interface of the capillary substrate with the bottom substrate and also a fluid-conducting arrangement for conducting a fluid through the capillary structure. The fluid-conducting arrangement may be designed for compartmenting the fluid by way of controlled pressure pulses. A linear sensor element, which extends toward a capillary of the capillary structure and/or away from it and/or along the capillary, and a fluid contact end of which and at least an adjacent part of its feed lie in an identical plane to the capillary, may be integrated in the microfluidic analysis device, the element finishing with its fluid contact end flush against a side wall of the capillary or extending into the hollow channel thereof.

Some embodiments of a blood coagulation testing system include an analyzer console device and a single-use cartridge component configured to releasably install into the console device. In some embodiments, the blood coagulation testing system can operate as an automated thromboelastometry system that is particularly useful, for example, at a point-of-care site.