A sample container of a thermal analyzer that performs thermogravimetry or calorimetry includes a bottomed cylindrical body portion and a cover portion abutting against an opening of the body portion and covering at least a part of the opening. The cover portion includes a first cover portion abutting against an edge portion of the opening and having a second opening in a part of the first cover portion, and a second cover portion separated from the first cover portion in an axial direction of the body portion so as to cover at least a part of the second opening.

A method of determining a concentration of plastic or other material not dissolved by silicon etchants contaminating a silicon product comprising: obtaining a sample of the silicon product contaminated with the plastic or other material not dissolved by silicon etchants; placing the sample of the silicon product into a ultrasonic bath liquid to produce a slurry comprising the ultrasonic bath liquid, silicon dust, and the plastic or other material not dissolved by silicon etchants; filtering the slurry with a first filter to produce a cake comprising the silicon dust and the plastic or other material not dissolved by silicon etchants separated from the sample of the silicon product; and analyzing the cake to determine the concentration of plastic or other material not dissolved by silicon etchants contaminating the silicon product.

A method of determining a concentration of plastic or other material not dissolved by silicon etchants contaminating a silicon product comprising: obtaining a sample of the silicon product contaminated with the plastic or other material not dissolved by silicon etchants; placing the sample of the silicon product into a ultrasonic bath liquid to produce a slurry comprising the ultrasonic bath liquid, silicon dust, and the plastic or other material not dissolved by silicon etchants; filtering the slurry with a first filter to produce a cake comprising the silicon dust and the plastic or other material not dissolved by silicon etchants separated from the sample of the silicon product; and analyzing the cake to determine the concentration of plastic or other material not dissolved by silicon etchants contaminating the silicon product.

Methods of preparing dispersions of carbon-based materials are disclosed herein. In some embodiments, a method comprises exposing the carbon-based material to an atmosphere comprising between about 0.5% v/v and about 5.0% v/v of oxygen for a selected time at an oxidation temperature to obtain a thermally oxidized material; and dispersing the thermally oxidized material in a liquid medium.

Methods of preparing dispersions of carbon-based materials are disclosed herein. In some embodiments, a method comprises exposing the carbon-based material to an atmosphere comprising between about 0.5% v/v and about 5.0% v/v of oxygen for a selected time at an oxidation temperature to obtain a thermally oxidized material; and dispersing the thermally oxidized material in a liquid medium.

With a water, particulate and fibre mixture, a method of quantifying fibre content may include providing a sample of the mixture, filtering the sample to produce a particulate and fibre mixture, burning the particulate and fibre mixture to produce a fibre sample, and dissolving the fibre sample to produce a fibre solution. The fibre solution may be analyzed to determine an elemental content of the fibre solution. The elemental content may be compared to a known elemental content to estimate the fibre content.

With a water, particulate and fibre mixture, a method of quantifying fibre content may include providing a sample of the mixture, filtering the sample to produce a particulate and fibre mixture, burning the particulate and fibre mixture to produce a fibre sample, and dissolving the fibre sample to produce a fibre solution. The fibre solution may be analyzed to determine an elemental content of the fibre solution. The elemental content may be compared to a known elemental content to estimate the fibre content.

The disclosure relates to a survey method of soil carbon stock in vegetated coastal wetlands, which excludes the influence of plant's fine roots when estimating the soil carbon stock, and effectively avoids double counting organic carbon stock of the fine roots in soil carbon stock surveys. At the same time, this method does not require bulk density calculation, which reduces the influence of sample volume compression during sample processing when calculating bulk density and provides a more accurate survey method for the study of coastal wetland carbon stock.

A sample is analyzed by temperature-modulated thermogravimetric analysis (TMTGA), using a thermogravimetric analysis (TGA) instrument. The TGA instrument comprises a furnace arranged in a furnace housing and an electronic balance with a load receiver arranged in a balance housing, wherein the load receiver extends into the furnace housing. A measuring position is arranged at one end of the load receiver within the furnace housing. A control unit controls the balance and/or the furnace. The TMTGA method includes at least using the TGA instrument to subject the sample to a temperature program that varies the temperature of the furnace and provides temperature-time setpoints for controlling the sample temperature, measuring the mass change of the sample as a function of time, and determining at least one kinetic parameter of the sample based on mass change. The temperature program may be stochastic and/or event-controlled in nature.

A sample is analyzed by temperature-modulated thermogravimetric analysis (TMTGA), using a thermogravimetric analysis (TGA) instrument. The TGA instrument comprises a furnace arranged in a furnace housing and an electronic balance with a load receiver arranged in a balance housing, wherein the load receiver extends into the furnace housing. A measuring position is arranged at one end of the load receiver within the furnace housing. A control unit controls the balance and/or the furnace. The TMTGA method includes at least using the TGA instrument to subject the sample to a temperature program that varies the temperature of the furnace and provides temperature-time setpoints for controlling the sample temperature, measuring the mass change of the sample as a function of time, and determining at least one kinetic parameter of the sample based on mass change. The temperature program may be stochastic and/or event-controlled in nature.