A test device for testing an oxidation potential of an electrolyte is provided. The test device comprises a cavity, a test unit, a detector, a processing unit, and a display. The test unit comprises a positive plate comprising a first through hole, a negative plate comprising a second through hole, a first infrared window covering the first through hole, a second infrared window covering the second through hole, and an electrolyte located between the positive electrode plate and the negative electrode plate. The first through hole and the second through hole penetrate each other. The first infrared window, the positive plate, the negative plate, and the second infrared window are stacked with each other. An infrared light beam passes through the first infrared window, the first through hole, the electrolyte, the second through hole, and the second infrared window in sequence and then is detected by the detector.

A method for assessing polymeric additive content A in a polymeric particle mixture may comprise determining a concentration B of a metal cation in a polymeric particle mixture comprising parent polymeric particles and polymeric additive particles, wherein the metal cation is selected from alkali earth metals and alkali metals, other than sodium (Na), and the metal cation is capable of forming a water-soluble base; determining a concentration C of the metal cation in the parent polymeric particles; determining a concentration D of the metal cation in the polymeric additive particles; and calculating a polymeric additive content A using formula A=(B−C)/D.

The present invention relates generally to the field of plastic microparticles. In particular, the present invention relates to the detection of plastic microparticles in a water-based sample. An embodiment of the present invention relates to a process for detecting and characterizing plastic microparticles in a water-based sample comprising the analysis of the sample by spectral flow cytometry. In accordance with the present invention, the process described herein may comprise the processing of the recorded flow cytometry data by a machine learning algorithm that can distinguish and categorize each particle based on its unique spectrum to characterize, for example, the plastic microparticles.

A method for producing a formed product using a resin composition including a plurality of raw materials, in which the content of raw materials in the resin composition is measured in real time, the method comprising the steps of: supplying each of the plurality of raw materials to an extruder; melt-kneading the plurality of raw materials in the extruder to prepare a resin composition; and irradiating the prepared resin composition with radiation and calculating the content of the raw material in the resin composition based on the results of detection of the radiation transmitted through the resin composition.

A method for evaluating physical properties of a melt-blown plastic resin, and, more specifically, to a novel method for evaluating physical properties are provided. When a particular plastic resin is processed by a melt-blown process, a stretching diameter value after the process of the plastic resin can be accurately derived from a physical property value measured using a specimen of the resin.

An apparatus for measuring a viscosity of a fluid is disclosed. The apparatus includes a Parylene coated quartz tuning fork for immersion in the fluid and an electronic circuit to excite a vibration of the Parylene coated quartz tuning fork and measure one or more vibrational parameters of the Parylene coated quartz tuning fork. A computer processor is configured to determine a non-Newtonian viscosity from the vibration of the Parylene coated quartz tuning fork based, at least in part, on a Stokes flow hydrodynamic model. The computer processor is coupled to a memory for storing a calibration curve to determine a Newtonian viscosity of the fluid from the non-Newtonian viscosity of the fluid.

Provided is an identification method of plastic microparticles, including: performing an infrared analysis on plastic microparticles to identify whether the plastic microparticles include polyethylene terephthalate, polyethylene, polypropylene, or nylon 66, wherein the identification is to determine whether the plastic microparticles have a characteristic peak of each plastic, and the characteristic peak is selected from signals that do not overlap and interfere with each other in the infrared spectrum signals of each plastic.

A method for evaluating long-term durability of a resin for piping is provided. Unlike the conventional FNCT evaluation method requiring a long period of time, the method disclosed herein is capable of predicting long-term durability of a resin for piping in a short time, by a simple calculation using a content of tie molecules, an entanglement molecular weight (M.sub.e) and a content of ultrahigh molecular weight components. In addition, the olefinic polymer is configured to have a predetermined relationship in relation to the content of tie molecules, the entanglement molecular weight (M.sub.e) and the content of ultrahigh molecular weight components, whereby the polymer of the present application can be used in the manufacture of a heating pipe requiring excellent long-term durability.

A method for evaluating long-term durability of a resin for piping is provided. Unlike the conventional FNCT evaluation method requiring a long period of time, the method disclosed herein is capable of predicting long-term durability of a resin for piping in a short time, by a simple calculation using a content of tie molecules, an entanglement molecular weight (M.sub.e) and a content of ultrahigh molecular weight components. In addition, the olefinic polymer is configured to have a predetermined relationship in relation to the content of tie molecules, the entanglement molecular weight (M.sub.e) and the content of ultrahigh molecular weight components, whereby the polymer of the present application can be used in the manufacture of a heating pipe requiring excellent long-term durability.

An analysis method is provided, wherein a measurement sample containing a diamine and an acid dianhydride can be obtained without a separate methyl derivatization process. The analysis method includes pretreating a polyimide film including the polyimide which is a poorly soluble polymer with DMAc after hydrolysis, and determining an amount of monomers contained in the polyimide film.