E37.10 - Fundamental, Statistical and Mechanical Properties

SIGNIFICANCE AND USE
5.1 Coefficients of linear thermal expansion are used, for example, for design purposes and to determine if failure by thermal stress may occur when a solid body composed of two different materials is subjected to temperature variations.  
5.2 This test method is comparable to Test Method D3386 for testing electrical insulation materials, but it covers a more general group of solid materials and it defines test conditions more specifically. This test method uses a smaller specimen and substantially different apparatus than Test Methods E228 and D696.  
5.3 This test method may be used in research, specification acceptance, regulatory compliance, and quality assurance.
SCOPE
1.1 This test method determines the technical coefficient of linear thermal expansion of solid materials using thermomechanical analysis techniques.  
1.2 This test method is applicable to solid materials that exhibit sufficient rigidity over the test temperature range such that the sensing probe does not produce indentation of the specimen.  
1.3 The recommended lower limit of coefficient of linear thermal expansion measured with this test method is 5 μm/(m·°C). The test method may be used at lower (or negative) expansion levels with decreased accuracy and precision (see Section 12).  
1.4 This test method is applicable to the temperature range from −120 °C to 900 °C. The temperature range may be extended depending upon the instrumentation and calibration materials used.  
1.5 SI units are the standard. No other units of measurement are included in this standard.  
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method calibrates or demonstrates conformity of a dynamic mechanical analyzer at an isothermal temperature within the range of –100 °C to 300 °C.  
5.2 Dynamic mechanical analysis experiments often use temperature ramps. This method does not address the effect of that change in temperature on the storage modulus.  
5.3 A calibration factor may be required to obtain corrected storage modulus values.  
5.4 This method may be used in research and development, specification acceptance, and quality control or assurance.
SCOPE
1.1 This test method describes the calibration or performance confirmation for the storage modulus scale of a commercial or custom built dynamic mechanical analyzer (DMA) over the temperature range of –100 °C to 300 °C using reference materials in the range of 1 GPa to 200 GPa.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Data obtained by this test method shall not be used to predict the behavior of materials at elevated temperatures except in applications in which the conditions of time, temperature, method of loading, and stress are similar to those specified in the test.  
5.2 This standard is particularly suited for quality control and development work. The data are not intended for use in design or predicting endurance at elevated temperatures.
SCOPE
1.1 This test method describes the determination of the temperature at which the specific modulus of a test specimen is realized by deflection in three-point bending. This temperature is identified as the distortion temperature. The distortion temperature is that temperature at which a test specimen of defined geometry deforms to a level of strain under applied stress of 0.455 MPa (66 psi) (Method A) and 1.82 MPa (264 psi) (Method B) equivalent to those used in Test Method D648. The test is applicable over the range of temperature from ambient to 300 °C.
Note 1: This test method is intended to provide results similar to those of Test Method D648 but is performed on a thermomechanical analyzer using a smaller test specimen. Equivalence of results to those obtained by Test Method D648 has been demonstrated on a limited number of materials. The results of this test method shall be considered to be independent and unrelated to those of Test Method D648 unless the user demonstrates equivalence.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method can be used to locate the glass transition region and assign a glass transition temperature of amorphous and semi-crystalline materials.  
5.2 Dynamic mechanical analyzers monitor changes in the viscoelastic properties of a material as a function of temperature and frequency, providing a means to quantify these changes. In ideal cases, the temperature of the onset of the decrease in storage modulus marks the glass transition.  
5.3 The glass transition takes place over a temperature range. This method assigns a single temperature (Tg) to represent that temperature range as measured by dynamic mechanical analysis. Tg may be determined by a variety of techniques and may vary according to that technique.  
5.4 A glass transition temperature (Tg) is useful in characterizing many important physical attributes of thermoplastic, thermosets, and semi-crystalline materials including their thermal history, processing conditions, physical stability, progress of chemical reactions, degree of cure, and both mechanical and electrical behavior.  
5.5 This test method is useful for quality control, specification acceptance, and research.
SCOPE
1.1 This test method covers the assignment of a glass transition temperature (Tg) of materials using dynamic mechanical analyzers.  
1.2 This test method is applicable to thermoplastic polymers, thermoset polymers, and partially crystalline materials which are thermally stable in the glass transition region.  
1.3 The applicable range of temperatures for this test method is dependent upon the instrumentation used, but, in order to encompass all materials, the minimum temperature should be about −150 °C.  
1.4 This test method is intended for materials having an elastic modulus in the range of 0.5 MPa to 100 GPa.  
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method may be used to determine and validate the performance of a particular thermomechanical analyzer apparatus.  
5.2 This test method may be used to determine and validate the performance of a particular method based upon thermomechanical analyzer temperature or length change measurements.  
5.3 This test method may be used to determine the repeatability of a particular apparatus, operator, or laboratory.  
5.4 This test method may be used for specification and regulatory compliance purposes.
SCOPE
1.1 This test method provides procedures for validating temperature and length change measurements of thermomechanical analyzers (TMA) and analytical methods based upon the measurement of temperature and length change. Performance parameters include temperature repeatability, linearity, and bias; and dimension change repeatability, detection limit, quantitation limit, linearity, and bias.  
1.2 Validation of apparatus performance and analytical methods is a necessary requirement for quality initiatives. Results may also be used for legal purposes.  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Most thermal analysis experiments are carried out under increasing temperature conditions where temperature is the independent parameter. Some experiments, however, are carried out under isothermal temperature conditions where the elapsed time to an event is measured as the independent parameter. Isothermal Kinetics (Test Methods E2070), Thermal Stability (Test Method E487), Oxidative Induction Time (OIT) (Test Methods D3895, D4565, D5483, E1858, and Specification D3350) and Loss-on-Drying (Test Methods E1868) are common examples of these kinds of experiments.  
5.2 Modern scientific instruments, including thermal analyzers, usually measure elapsed time with excellent precision and accuracy. In such cases, it may only be necessary to confirm the performance of the instrument by comparison to a suitable reference. Only rarely will it may be required to correct the calibration of an instrument's elapsed time signal through the use of a calibration factor.  
5.3 It is necessary to obtain elapsed time signal conformity only to 0.1 times the repeatability relative standard deviation (standard deviation divided by the mean value) expressed as a percent for the test method in which the thermal analyzer is to be used. For those test methods listed in Section 2 this conformity is 0.1 %.
SCOPE
1.1 This test method describes the calibration or performance confirmation of the elapsed-time signal from thermal analyzers.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Performance verification or calibration is essential to the accurate determination of quantitative dimension change measurements.  
5.2 This test method may be used for instrument performance validation, regulatory compliance, research and development and quality assurance purposes.
SCOPE
1.1 This test method describes calibration of the length change (deflection) measurement or thermal expansion of thermomechanical analyzers (TMAs) within the temperature range from –150 °C to 1000 °C using the thermal expansion of a suitable reference material.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Thermomechanical analyzers are employed in their various modes of operation (penetration, expansion, flexure, etc.) to characterize a wide range of materials. In most cases, the value to be assigned in thermomechanical measurements is the temperature of the transition (or event) under study. Therefore, the temperature axis (abscissa) of all TMA thermal curves must be accurately calibrated either by direct reading of a temperature sensor or by adjusting the programmer temperature to match the actual temperature over the temperature range of interest.
SCOPE
1.1 This test method describes the temperature calibration of thermomechanical analyzers from −50 °C to 1500 °C. (See Note 1.)  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 Warning—Mercury has been designated by many regulatory agencies as a hazardous substance that can cause serious medical issues. Mercury, or its vapor, has been demonstrated to be hazardous to health and corrosive to materials. Use caution when handling mercury and mercury-containing products. See the applicable product Safety Data Sheet (SDS) for additional information. The potential exists that selling mercury or mercury-containing products, or both, is prohibited by local or national law. Users must determine legality of sales in their location.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Specific precautionary statements are given in Section 7 and Note 12.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Differing temperature rates-of-change may be required for different measurements (for example, Test Method E698). Temperature calibration changes as a function of temperature rate-of-change. The use of the known thermal lag of an apparatus may be used to adjust the temperature calibration of the apparatus obtained at one temperature rate-of-change with that at another required for a given applications. This adjustment procedure for temperature calibration is described in 8.1.  
5.2 This test method may be used in research, quality assurance, and specification acceptance.
SCOPE
1.1 This test method addresses the dependence of temperature calibration on the temperature rate-of-change. This test method describes the determination of the thermal lag of thermal analysis apparatus and its application to the modification of the temperature calibration for that apparatus obtained at alternative linear temperature rates-of-change.  
1.2 This test method is applicable, but not limited to, the temperature calibration of differential thermal analyzers (DTAs), differential scanning calorimeters (DSCs), thermogravimetric analyzers (TGAs), thermomechanical analyzers (TMAs), and dynamic mechanical analyzers (DMAs).  
1.3 This test method is applicable only to apparatus demonstrating a linear relationship between indicated temperature and temperature rate-of-change.  
1.4 The values stated in SI units are to be regarded as the standard. No other units of measurement are included in this standard.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Thermal conductivity is a useful design parameter for the rate of heat transfer through a material.  
5.2 The results of this test method may be used for design purposes, service evaluation, manufacturing control, research and development, and hazard evaluation. (See Practice E1231.)
SCOPE
1.1 This test method describes the determination of thermal conductivity of homogeneous, non-porous solid materials in the range of 0.10 W/(K·m) to 1.0 W/(K·m) by modulated temperature differential scanning calorimeter. This range includes many polymeric, glass, and ceramic materials. Thermal diffusivity, which is related to thermal conductivity through specific heat capacity and density, may also be derived. Thermal conductivity and diffusivity can be determined at one or more temperatures over the range of 0 °C to 90 °C.  
1.2 The values stated in SI units are to be regarded as standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The standard deviation, or one of its derivatives, such as relative standard deviation or pooled standard deviation, derived from this practice, provides an estimate of precision in a measured value. Such results are ordinarily expressed as the mean value ± the standard deviation, that is, X ± s.  
5.2 If the measured values are, in the statistical sense, “normally” distributed about their mean, then the meaning of the standard deviation is that there is a 67 % chance, that is 2 in 3, that a given value will lie within the range of ± one standard deviation of the mean value. Similarly, there is a 95 % chance, that is 19 in 20, that a given value will lie within the range of ± two standard deviations of the mean. The two standard deviation range is sometimes used as a test for outlying measurements.  
5.3 The calculation of precision in the slope and intercept of a line, derived from experimental data, commonly is required in the determination of kinetic parameters, vapor pressure or enthalpy of vaporization. This practice describes how to obtain these and other statistically derived values associated with measurements by thermal analysis.
SCOPE
1.1 This practice details the statistical data treatment used in some thermal analysis methods.  
1.2 The method describes the commonly encountered statistical tools of the mean, standard derivation, relative standard deviation, pooled standard deviation, pooled relative standard deviation, the best fit to a (linear regression of a) straight line (or plane), and propagation of uncertainties for all calculations encountered in thermal analysis methods (see Practice E2586).  
1.3 Some thermal analysis methods derive the analytical value from the slope or intercept of a linear regression straight line (or plane) assigned to three or more sets of data pairs. Such methods may require an estimation of the precision in the determined slope or intercept. The determination of this precision is not a common statistical tool. This practice details the process for obtaining such information about precision.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Dynamic mechanical analyzers monitor changes in the viscoelastic properties of a material as a function of temperature and frequency, providing a means to quantify these changes. In most cases, the value to be assigned is the temperature of the transition (or event) under study. Therefore, the temperature axis (abscissa) of dynamic mechanical analysis thermal curves must be accurately calibrated by adjusting the apparent temperature scale to match the actual specimen temperature over the temperature range of interest.  
5.2 This test method is useful for research, quality assurance, and specification acceptance.
SCOPE
1.1 These test methods describe the temperature calibration of dynamic mechanical analyzers (DMA) from –100 °C to 300 °C.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The glass transition is dependent on the thermal history of the material to be tested. For amorphous and semicrystalline materials the assignment of the glass transition temperature may lead to important information about thermal history, processing conditions, stability, progress of chemical reactions, and mechanical and electrical behavior.  
5.2 Thermomechanical analysis provides a rapid means of detecting changes in hardness or linear expansion associated with the glass transition.  
5.3 This test method is useful for research and development, quality control, and specification acceptance.
SCOPE
1.1 This test method describes procedures for the assignment of the glass transition temperature of materials on heating using thermomechanical measurements under compression experimental conditions.  
1.2 This test method is applicable to amorphous or to partially crystalline materials that are sufficiently rigid below the glass transition to inhibit indentation by the sensing probe.  
1.3 The normal operating temperature range is from −100 °C to 600 °C. This temperature range may be extended depending upon the instrumentation used.  
1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Specific precautionary statements are given in Section 7.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method provides a means of characterizing the mechanical behavior of materials using very small amounts of material including thermoplastic and thermoset polymers, composites, and metals.  
5.2 The data obtained may be used for research and development and establishment of optimum processing conditions. The data are not intended for use in design or for predicting performance.
Note 2: This test method may not be suitable for anisotropic materials.
SCOPE
1.1 This test method describes the use of linear controlled-rate-of-loading in three-point bending to determine the elastic modulus of isotropic specimens in the form of rectangular bars using a thermomechanical analyzer (TMA).
Note 1: This method is intended to provide results similar to those of Test Methods D790 or D5934 but is performed on a thermomechanical analyzer using smaller test specimens. Until the user demonstrates equivalence, the results of this method shall be considered independent and unrelated to those of Test Methods D790 or D5934.  
1.2 This test method provides a means for determining the elastic modulus within the linear region of the stress-strain curves (see Fig. 1). This test is conducted under isothermal temperature conditions from –100 °C to 300 °C.
FIG. 1 Stress-Strain Curve (Linear Region)  
1.3 Typical test specimens are in the form of thin strips 0.5 mm in thickness, 1.5 mm in width, and 6 mm in length. The size of the test specimen is limited by the distance between the supports used in the three-point bending mode of operation, commonly 0.5 cm.  
1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Dynamic mechanical analysis monitors changes in the viscoelastic properties (that is, storage modulus, loss modulus, tangent angle delta) of a material as a function of temperature and frequency, providing a means to quantify these changes. In many cases, the value to be assigned is the temperature of the transition or event under study. Therefore, the temperature axis (abscissa) of the dynamic mechanical analysis thermal curve must be accurately calibrated by adjusting the measured temperature scale to match the assumed specimen temperature over the temperature range of interest.
SCOPE
1.1 This test method describes the temperature calibration of a dynamic mechanical analyzer using thermal lag over the temperature range of –100 °C to 300 °C.  
1.2 This standard may be compared to Test Methods E1867.  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Most thermal analysis experiments are conducted under ambient pressure conditions using isothermal or temperature time rate of change conditions where time or temperature is the independent parameter. Some experiments, however, are conducted under reduced or elevated pressure conditions where pressure is an independent experimental parameter (Test Method E537). Oxidation Induction Times (Test Methods D5483, D5885, D6186, and E1858), Oxidation Onset Temperature (Test Method E2009), and the Vapor Pressure (Test Method E1782) are other examples of experiments conducted under elevated or reduced pressure (vacuum) conditions. Since in these cases pressure is an independent variable, the measurement system for this parameter shall be calibrated to ensure interlaboratory reproducibility.  
5.2 The dependence of experimental results on pressure is usually logarithmic rather than linear.
SCOPE
1.1 This test method describes the calibration or performance confirmation of the electronic pressure signals from thermal analysis apparatus.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method demonstrates conformity of a dynamic mechanical analyzer at an isothermal temperature of 21 °C.  
5.2 Dynamic mechanical analysis experiments often use linear temperature change. This test method does not address the effect of that change in temperature on the loss modulus.  
5.3 This test method may be used in research and development, specification acceptance, and quality control or assurance.
SCOPE
1.1 This test method describes the performance confirmation or measurement of conformance for the loss modulus scale of a commercial or custom-built dynamic mechanical analyzer (DMA) at 21 °C using ultra-high molecular weight polyethylene as a reference material.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method may be used to determine and validate the performance of a particular DSC apparatus.  
5.2 This test method may be used to determine and validate the performance of a particular method based upon a DSC temperature and enthalpic measurement, or both.  
5.3 This test method may be used to determine the repeatability of a particular apparatus, operator, or laboratory.  
5.4 This test method may be used for specification and regulatory compliance purposes.
SCOPE
1.1 This test method provides procedures for validating temperature and enthalpy measurements of differential scanning calorimeters (DSC) and analytical methods based upon the measurement of temperature or enthalpy (or heat), or both, by DSC. Performance parameters determined include temperature and calorimetric repeatability (precision), detection limit, quantitation limit, linearity, and bias. This test method is applicable to exothermic events.  
1.2 Validation of apparatus performance and analytical methods is requested or required for quality initiatives or where results may be used for legal purposes.  
1.3 The values stated in SI units are to regarded as standard. No other units of measurement are included in this standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Data obtained by this test method shall not be used to predict the behavior of materials at elevated temperatures except in applications in which the conditions of time, temperature, method of loading, and stress are similar to those specified in the test.  
5.2 This test method is particularly suited for quality control and development work. The data are not intended for use in design or predicting endurance at elevated temperatures.  
5.3 Ruggedness testing indicates that some materials, such as poly (vinyl chloride) exhibit substantially greater imprecision than that described in Section 14 for “well behaved” materials.
SCOPE
1.1 This test method is applicable to high modulus materials that soften upon heating to a modulus less than 6.0 MPa. This test method describes the determination of the temperature at which the specific modulus of either 6.65 MPa (Method A) or 33.3 MPa (Method B) (equivalent to Test Method D1525) of a test specimen is realized by indentation measurement using a thermomechanical analyzer as the test specimen is heated. This temperature is identified as the indentation softening temperature. The test may be performed over the temperature range of ambient to 300 °C.
Note 1: This test method is intended to provide results similar to those of Test Method D1525 but is performed on a thermomechanical analyzer using a smaller diameter indenting probe. Equivalence of results to those obtained by Test Method D1525 has been demonstrated on a limited number of materials. Until the user demonstrates equivalence, the results of this Test Method shall be considered to be independent and unrelated to those of Test Method D1525.  
1.2 This test method is not recommended for ethyl cellulose, poly (vinyl chloride), poly (vinylidene chloride) and other materials having a large measurement imprecision (see Test Method D1525 and 5.3 and Section 14).  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

ABSTRACT
This practice describes the calculation of the heat of vaporization of a liquid or the heat of sublimation of a solid from measured vapor pressure data. It is applicable to pure liquids, azeotropes, pure solids, and homogenous solid solutions over the temperature range for which the vapor pressure equation fitted to the measured data is applicable. Vapor pressure data shall be measured in accordance to the test methods and shall be correlated with the Antoine equation. The heat of vaporization or sublimation is computed at the desired temperature from the vapor-pressure temperature derivative from the fitted Antoine equation by use of the Clapeyron equation.
SCOPE
1.1 This practice describes the calculation of the heat of vaporization of a liquid or the heat of sublimation of a solid from measured vapor pressure data. It is applicable to pure liquids, azeotropes, pure solids, and homogenous solid solutions over the temperature range for which the vapor pressure equation fitted to the measured data is applicable.  
Note 1: This practice is generally not applicable to liquid mixtures. For a pure liquid or azeotrope, composition does not change upon vaporization so that the integral heat of vaporization is identical to the differential heat of vaporization. Non-azeotropic liquid mixtures change composition upon vaporizing. Heat of vaporization data computed from this practice for a liquid mixture are valid only as an approximation to the mixture differential heat of vaporization; it is not a valid approximation to the mixture integral heat of vaporization.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Most thermomechanical analysis experiments are carried out with some force applied to the test specimen. This force is often created electronically. It may be constant or changed during the experiment.  
5.2 This method demonstrates conformance or calibrates the electronically applied force signal.  
5.3 This method may be used for research and development, quality control, manufacturing or regulatory applications.  
5.4 Other thermomechanical analyzer calibration functions include temperature by Test Method E1363 and length change by Test Method E2113.
SCOPE
1.1 This test method describes the calibration or performance confirmation of the electronically applied force signal for thermomechanical analyzers over the range of 0 N to 1 N.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Thermogravimetry provides a rapid method for the determination of the temperature-decomposition profile of a material.  
5.2 This practice is useful for quality control, specification acceptance, and research.  
5.3 This practice is intended to provide an accelerated thermal endurance estimation in a fraction of the time require for oven-aging tests. The primary product of this practice is the thermal index (temperature) for a selected estimated thermal endurance (time) as derived from material decomposition.  
5.4 Alternatively, the estimated thermal endurance (time) of a material may be estimated from a selected thermal index (temperature).  
5.5 Additionally, the thermal endurance of a material at selected failure time and temperature may be estimated when compared to a reference value for thermal endurance and thermal index obtained from electrical or mechanical oven aging tests.  
5.6 This practice shall not be used for product lifetime predications unless a correlation between test results and actual lifetime has been demonstrated. In many cases, multiple mechanisms occur during the decomposition of a material, with one mechanism dominating over one temperature range, and a different mechanism dominating in a different temperature range. Users of this practice are cautioned to demonstrate for their system that any temperature extrapolations are technically sound.
SCOPE
1.1 This practice describes the determination of thermal endurance, thermal index, and relative thermal index for organic materials using the Arrhenius activation energy generated for thermal decomposition measured by thermogravimetry.  
1.2 This practice is generally applicable to materials with a well-defined thermal decomposition profile upon heating, namely a smooth, continuous mass change.  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
4.1 Section 5 identifies essential instrumentation and accessories required to perform thermal analysis, rheometry, or viscometry for a variety of different instruments. The appropriate generic instrument description should be included in any test method describing use or application of the thermal analysis, rheometry, or viscometry instrumentation described herein.  
4.2 Units included in these descriptions are used to identify needed performance criteria and are considered typical. Other units may be used when including these descriptions in a specific test method. Items underlined constitute required inputs specifically established for each test method (for example, sensitivity of temperature sensor).  
4.3 Additional components and accessories may be added as needed, with the appropriate performance requirements specified. Items listed in these descriptions but not used in a test method (for example, vacuum system) may be deleted.
SCOPE
1.1 This practice describes generic descriptions of apparatus used for thermal analysis or rheometry measurements and its purpose is to achieve uniformity in description of thermal analysis, rheometry, and viscometer instrumentation throughout standard test methods. These descriptions are intended to be used as templates for inclusion in any test method where the thermal analysis instrumentation described herein is cited.  
1.2 Each description contains quantifiable instrument performance requirements to be specified for each test method.  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 These test methods calibrate or demonstrate conformity of the humidity level in a purge gas generated by a humidity generator at a fixed temperature. Such calibration or demonstration of conformity may be required by quality initiatives.  
5.2 Conformance demonstrates that the humidified purge gas is within some established limits.  
5.3 Calibration provides an offset and or slope value that may be used for establishing the relative humidity scale of the apparatus.
SCOPE
1.1 These test methods describe the humidity calibration (or conformance) of humidity generators for use with thermogravimetric analyzers and other thermal analysis apparatus. The humidity range covered is 5 % relative humidity (% RH) to 95 % RH and the temperature range is 0 °C to 80 °C.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method may be used to validate the performance of a specific thermogravimetric analyzer.  
5.2 This test method may be used to validate the performance of a specific method based upon a thermogravimetry mass loss or residue measurement.  
5.3 This test method may be used to determine the repeatability of a specific apparatus, operator, or laboratory.  
5.4 This test method may be used for specification and regulatory compliance purposes.
SCOPE
1.1 This test method provides procedures for validating mass loss, residue, and temperature measurements by thermogravimetric analyzers (TGAs) and analytical methods based upon the measurement of mass loss or residue content or temperature. Performance parameters determined include mass loss, residue, and temperature repeatability (precision), detection limit, quantitation limit, linearity, and bias.  
1.2 Validation of apparatus performance and analytical methods is requested or required for quality initiatives or where results may be used for legal purposes.  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The glass transition is dependent on the thermal history, softening agents or additives of the material to be tested. For amorphous and semicrystalline materials the assignment of a glass transition temperature may lead to important information about thermal history, processing conditions, stability, progress of chemical reactions, and mechanical and electrical behavior.  
5.2 Thermomechanical analysis provides a rapid means of detecting changes in hardness or linear dimensional change associated with the glass transition. Dimensional changes measured as a specimen is heated over the glass transition region may include the interaction of several effects: an increase in the coefficient of expansion, a decrease in the modulus, which under a constant stress leads to increased extension, stress relief leading to irreversible dimensional change (shrinkage in one dimension, expansion in another dimension), and physical aging effects which change the kinetics of the dimensional change.  
5.3 This test method is useful for research and development, quality control, and specification acceptance testing; particularly of films and fibers.
SCOPE
1.1 This test method describes a procedure for the assignment of a glass transition temperature (Tg) of materials on heating using thermomechanical measurements in tension.  
1.2 This test method may be used as a complement to Test Method E1545 and is applicable to amorphous or to partially crystalline materials in the form of films, fibers, wires, etc., that are sufficiently rigid to inhibit extension during loading at ambient temperature.  
1.3 The generally applicable temperature range for this test method is 25 °C to 600 °C. This temperature range may be altered depending upon the instrumentation used.  
1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method calibrates or demonstrates conformity of a dynamic mechanical analyzer at an isothermal temperature within the range of –100 °C to 300 °C.  
5.2 Dynamic mechanical analysis experiments often use temperature ramps. This method does not address the effect of that change in temperature on the storage modulus.  
5.3 A calibration factor may be required to obtain corrected storage modulus values.  
5.4 This method may be used in research and development, specification acceptance, and quality control or assurance.
SCOPE
1.1 This test method describes the calibration or performance confirmation for the storage modulus scale of a commercial or custom built dynamic mechanical analyzer (DMA) over the temperature range of –100 °C to 300 °C using reference materials in the range of 1 GPa to 200 GPa.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The standard deviation, or one of its derivatives, such as relative standard deviation or pooled standard deviation, derived from this practice, provides an estimate of precision in a measured value. Such results are ordinarily expressed as the mean value ± the standard deviation, that is, X ± s.  
5.2 If the measured values are, in the statistical sense, “normally” distributed about their mean, then the meaning of the standard deviation is that there is a 67 % chance, that is 2 in 3, that a given value will lie within the range of ± one standard deviation of the mean value. Similarly, there is a 95 % chance, that is 19 in 20, that a given value will lie within the range of ± two standard deviations of the mean. The two standard deviation range is sometimes used as a test for outlying measurements.  
5.3 The calculation of precision in the slope and intercept of a line, derived from experimental data, commonly is required in the determination of kinetic parameters, vapor pressure or enthalpy of vaporization. This practice describes how to obtain these and other statistically derived values associated with measurements by thermal analysis.
SCOPE
1.1 This practice details the statistical data treatment used in some thermal analysis methods.  
1.2 The method describes the commonly encountered statistical tools of the mean, standard derivation, relative standard deviation, pooled standard deviation, pooled relative standard deviation, the best fit to a (linear regression of a) straight line, and propagation of uncertainties for all calculations encountered in thermal analysis methods (see Practice E2586).  
1.3 Some thermal analysis methods derive the analytical value from the slope or intercept of a linear regression straight line assigned to three or more sets of data pairs. Such methods may require an estimation of the precision in the determined slope or intercept. The determination of this precision is not a common statistical tool. This practice details the process for obtaining such information about precision.  
1.4 There are no ISO methods equivalent to this practice.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Coefficients of linear thermal expansion are used, for example, for design purposes and to determine if failure by thermal stress may occur when a solid body composed of two different materials is subjected to temperature variations.  
5.2 This test method is comparable to Test Method D3386 for testing electrical insulation materials, but it covers a more general group of solid materials and it defines test conditions more specifically. This test method uses a smaller specimen and substantially different apparatus than Test Methods E228 and D696.  
5.3 This test method may be used in research, specification acceptance, regulatory compliance, and quality assurance.
SCOPE
1.1 This test method determines the technical coefficient of linear thermal expansion of solid materials using thermomechanical analysis techniques.  
1.2 This test method is applicable to solid materials that exhibit sufficient rigidity over the test temperature range such that the sensing probe does not produce indentation of the specimen.  
1.3 The recommended lower limit of coefficient of linear thermal expansion measured with this test method is 5 μm/(m·°C). The test method may be used at lower (or negative) expansion levels with decreased accuracy and precision (see Section 11).  
1.4 This test method is applicable to the temperature range from −120 °C to 900 °C. The temperature range may be extended depending upon the instrumentation and calibration materials used.  
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method may be used to determine and validate the performance of a particular thermomechanical analyzer apparatus.  
5.2 This test method may be used to determine and validate the performance of a particular method based upon thermomechanical analyzer temperature or length change measurements.  
5.3 This test method may be used to determine the repeatability of a particular apparatus, operator, or laboratory.  
5.4 This test method may be used for specification and regulatory compliance purposes.
SCOPE
1.1 This test method provides procedures for validating temperature and length change measurements of thermomechanical analyzers (TMA) and analytical methods based upon the measurement of temperature and length change. Performance parameters include temperature repeatability, linearity, and bias; and dimension change repeatability, detection limit, quantitation limit, linearity, and bias.  
1.2 Validation of apparatus performance and analytical methods is a necessary requirement for quality initiatives. Results may also be used for legal purposes.  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Thermomechanical analyzers are employed in their various modes of operation (penetration, expansion, flexure, etc.) to characterize a wide range of materials. In most cases, the value to be assigned in thermomechanical measurements is the temperature of the transition (or event) under study. Therefore, the temperature axis (abscissa) of all TMA thermal curves must be accurately calibrated either by direct reading of a temperature sensor or by adjusting the programmer temperature to match the actual temperature over the temperature range of interest.
SCOPE
1.1 This test method describes the temperature calibration of thermomechanical analyzers from −50 °C to 1500 °C. (See Note 1.)  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 Warning—Mercury has been designated by many regulatory agencies as a hazardous substance that can cause serious medical issues. Mercury, or its vapor, has been demonstrated to be hazardous to health and corrosive to materials. Use caution when handling mercury and mercury-containing products. See the applicable product Safety Data Sheet (SDS) for additional information. The potential exists that selling mercury or mercury-containing products, or both, is prohibited by local or national law. Users must determine legality of sales in their location.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. Specific precautionary statements are given in Section 7 and Note 11.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Data obtained by this test method shall not be used to predict the behavior of materials at elevated temperatures except in applications in which the conditions of time, temperature, method of loading, and stress are similar to those specified in the test.  
5.2 This standard is particularly suited for quality control and development work. The data are not intended for use in design or predicting endurance at elevated temperatures.
SCOPE
1.1 This test method describes the determination of the temperature at which the specific modulus of a test specimen is realized by deflection in three-point bending. This temperature is identified as the distortion temperature. The distortion temperature is that temperature at which a test specimen of defined geometry deforms to a level of strain under applied stress of 0.455 MPa (66 psi) (Method A) and 1.82 MPa (264 psi) (Method B) equivalent to those used in Test Method D648. The test is applicable over the range of temperature from ambient to 300 °C.
Note 1: This test method is intended to provide results similar to those of Test Method D648 but is performed on a thermomechanical analyzer using a smaller test specimen. Equivalence of results to those obtained by Test Method D648 has been demonstrated on a limited number of materials. The results of this test method shall be considered to be independent and unrelated to those of Test Method D648 unless the user demonstrates equivalence.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 These test methods calibrate or demonstrate conformity of the humidity level in a purge gas generated by a humidity generator at a fixed temperature. Such calibration or demonstration of conformity may be required by quality initiatives.  
5.2 Conformance demonstrates that the humidified purge gas is within some established limits.  
5.3 Calibration provides an offset and or slope value that may be used for establishing the relative humidity scale of the apparatus.
SCOPE
1.1 These test methods describe the humidity calibration (or conformance) of humidity generators for use with thermogravimetric analyzers and other thermal analysis apparatus. The humidity range covered is 5 % relative humidity (% RH) to 95 % RH and the temperature range is 0 °C to 80 °C.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 The glass transition is dependent on the thermal history, softening agents or additives of the material to be tested. For amorphous and semicrystalline materials the assignment of a glass transition temperature may lead to important information about thermal history, processing conditions, stability, progress of chemical reactions, and mechanical and electrical behavior.  
5.2 Thermomechanical analysis provides a rapid means of detecting changes in hardness or linear dimensional change associated with the glass transition. Dimensional changes measured as a specimen is heated over the glass transition region may include the interaction of several effects: an increase in the coefficient of expansion, a decrease in the modulus, which under a constant stress leads to increased extension, stress relief leading to irreversible dimensional change (shrinkage in one dimension, expansion in another dimension), and physical aging effects which change the kinetics of the dimensional change.  
5.3 This test method is useful for research and development, quality control, and specification acceptance testing; particularly of films and fibers.
SCOPE
1.1 This test method describes a procedure for the assignment of a glass transition temperature (Tg) of materials on heating using thermomechanical measurements in tension.  
1.2 This test method may be used as a complement to Test Method E1545 and is applicable to amorphous or to partially crystalline materials in the form of films, fibers, wires, etc., that are sufficiently rigid to inhibit extension during loading at ambient temperature.  
1.3 The generally applicable temperature range for this test method is −100 °C to 600 °C. This temperature range may be altered depending upon the instrumentation used.  
1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method may be used to determine and validate the performance of a particular thermomechanical analyzer apparatus.  
5.2 This test method may be used to determine and validate the performance of a particular method based upon thermomechanical analyzer temperature or length change measurements.  
5.3 This test method may be used to determine the repeatability of a particular apparatus, operator, or laboratory.  
5.4 This test method may be used for specification and regulatory compliance purposes.
SCOPE
1.1 This test method provides procedures for validating temperature and length change measurements of thermomechanical analyzers (TMA) and analytical methods based upon the measurement of temperature and length change. Performance parameters include temperature repeatability, linearity and bias; and dimension change repeatability, detection limit, quantitation limit, linearity and bias.  
1.2 Validation of apparatus performance and analytical methods is a necessary requirement for quality initiatives. Results may also be used for legal purposes.  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Most thermal analysis experiments are carried out under increasing temperature conditions where temperature is the independent parameter. Some experiments, however, are carried out under isothermal temperature conditions where the elapsed time to an event is measured as the independent parameter. Isothermal Kinetics (Test Methods E2070), Thermal Stability (Test Method E487), Oxidative Induction Time (OIT) (Test Methods D3895, D4565, D5483, E1858, and Specification D3350) and Loss-on-Drying (Test Methods E1868) are common examples of these kinds of experiments.  
5.2 Modern scientific instruments, including thermal analyzers, usually measure elapsed time with excellent precision and accuracy. In such cases, it may only be necessary to confirm the performance of the instrument by comparison to a suitable reference. Only rarely will it may be required to correct the calibration of an instrument's elapsed time signal through the use of a calibration factor.  
5.3 It is necessary to obtain elapsed time signal conformity only to 0.1 times the repeatability relative standard deviation (standard deviation divided by the mean value) expressed as a percent for the test method in which the thermal analyzer is to be used. For those test methods listed in Section 2 this conformity is 0.1 %.
SCOPE
1.1 This test method describes the calibration or performance confirmation of the elapsed-time signal from thermal analyzers.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 There is no ISO standard equivalent to this test method.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Differing temperature rates-of-change may be required for different measurements (for example, Test Method E698). Temperature calibration changes as a function of temperature rate-of-change. The use of the known thermal lag of an apparatus may be used to adjust the temperature calibration of the apparatus obtained at one temperature rate-of-change with that at another required for a given applications. This adjustment procedure for temperature calibration is described in 8.1.  
5.2 This test method may be used in research, quality assurance, and specification acceptance.
SCOPE
1.1 This test method addresses the dependence of temperature calibration on the temperature rate-of-change. This test method describes the determination of the thermal lag of thermal analysis apparatus and its application to the modification of the temperature calibration for that apparatus obtained at alternative linear temperature rates-of-change.  
1.2 This test method is applicable, but not limited to, the temperature calibration of differential thermal analyzers (DTAs), differential scanning calorimeters (DSCs), thermogravimetric analyzers (TGAs), thermomechanical analyzers (TMAs), and dynamic mechanical analyzers (DMAs).  
1.3 This test method is applicable only to apparatus demonstrating a linear relationship between indicated temperature and temperature rate-of-change.  
1.4 The values stated in SI units are to be regarded as the standard. No other units of measurement are included in this standard.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Dynamic mechanical analyzers monitor changes in the viscoelastic properties of a material as a function of temperature and frequency, providing a means to quantify these changes. In most cases, the value to be assigned is the temperature of the transition (or event) under study. Therefore, the temperature axis (abscissa) of dynamic mechanical analysis thermal curves must be accurately calibrated by adjusting the apparent temperature scale to match the actual specimen temperature over the temperature range of interest.  
5.2 This test method is useful for research, quality assurance, and specification acceptance.
SCOPE
1.1 These test methods describes the temperature calibration of dynamic mechanical analyzers (DMA) from –100 °C to 300 °C.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method can be used to locate the glass transition region and assign a glass transition temperature of amorphous and semi-crystalline materials.  
5.2 Dynamic mechanical analyzers monitor changes in the viscoelastic properties of a material as a function of temperature and frequency, providing a means to quantify these changes. In ideal cases, the temperature of the onset of the decrease in storage modulus marks the glass transition.  
5.3 The glass transition takes place over a temperature range. This method assigns a single temperature (Tg) to represent that temperature range as measured by dynamic mechanical analysis. Tg may be determined by a variety of techniques and may vary according to that technique.  
5.4 A glass transition temperature (Tg) is useful in characterizing many important physical attributes of thermoplastic, thermosets, and semi-crystalline materials including their thermal history, processing conditions, physical stability, progress of chemical reactions, degree of cure, and both mechanical and electrical behavior.  
5.5 This test method is useful for quality control, specification acceptance, and research.
SCOPE
1.1 This test method covers the assignment of a glass transition temperature (Tg) of materials using dynamic mechanical analyzers.  
1.2 This test method is applicable to thermoplastic polymers, thermoset polymers, and partially crystalline materials which are thermally stable in the glass transition region.  
1.3 The applicable range of temperatures for this test method is dependent upon the instrumentation used, but, in order to encompass all materials, the minimum temperature should be about −150 °C.  
1.4 This test method is intended for materials having an elastic modulus in the range of 0.5 MPa to 100 GPa.  
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method calibrates or demonstrates conformity of a dynamic mechanical analyzer at an isothermal temperature within the range of –100 °C to 300 °C.  
5.2 Dynamic mechanical analysis experiments often use temperature ramps. This method does not address the effect of that change in temperature on the storage modulus.  
5.3 A calibration factor may be required to obtain corrected storage modulus values.  
5.4 This method may be used in research and development, specification acceptance, and quality control or assurance.
SCOPE
1.1 This test method describes the calibration or performance confirmation for the storage modulus scale of a commercial or custom built dynamic mechanical analyzer (DMA) over the temperature range of –100 °C to 300 °C using reference materials in the range of 1 GPa to 200 GPa.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method provides a means of characterizing the mechanical behavior of materials using very small amounts of material.  
5.2 The data obtained may be used for quality control, research and development and establishment of optimum processing conditions. The data are not intended for use in design or predicting performance.
Note 2: This test method may not be suitable for anisotropic materials.
SCOPE
1.1 This test method describes the use of linear controlled-rate-of-loading in three-point bending to determine the elastic modulus of isotropic specimens in the form of rectangular bars using a thermomechanical analyzer (TMA).
Note 1: This method is intended to provide results similar to those of Test Methods D790 or D5934 but is performed on a thermomechanical analyzer using smaller test specimens. Until the user demonstrates equivalence, the results of this method shall be considered independent and unrelated to those of Test Methods D790 or D5934.  
1.2 This test method provides a means for determining the elastic modulus within the linear region of the stress-strain curves (see Fig. 1). This test is conducted under isothermal temperature conditions from –100 °C to 300 °C.
FIG. 1 Stress-Strain Curve (Linear Region)  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Performance verification or calibration is essential to the accurate determination of quantitative dimension change measurements.  
5.2 This test method may be used for instrument performance validation, regulatory compliance, research and development and quality assurance purposes.
SCOPE
1.1 This test method describes calibration of the length change (deflection) measurement or thermal expansion of thermomechanical analyzers (TMAs) within the temperature range from –150 °C to 1000 °C using the thermal expansion of a suitable reference material.  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Data obtained by this test method shall not be used to predict the behavior of materials at elevated temperatures except in applications in which the conditions of time, temperature, method of loading, and stress are similar to those specified in the test.  
5.2 This standard is particularly suited for quality control and development work. The data are not intended for use in design or predicting endurance at elevated temperatures.
SCOPE
1.1 This test method describes the determination of the temperature at which the specific modulus of a test specimen is realized by deflection in three-point bending. This temperature is identified as the distortion temperature. The distortion temperature is that temperature at which a test specimen of defined geometry deforms to a level of strain under applied stress of 0.455 MPa (66 psi) (Method A) and 1.82 MPa (264 psi) (Method B) equivalent to those used in Test Method D648. The test is applicable over the range of temperature from ambient to 300 °C.
Note 1: This test method is intended to provide results similar to those of Test Method D648 but are performed on a thermomechanical analyzer using a smaller test specimen. Equivalence of results to those obtained by Test Method D648 has been demonstrated on a limited number of materials. The results of this test method shall be considered to be independent and unrelated to those of Test Method D648 unless the user demonstrates equivalence.  
1.2 There is no ISO standard equivalent to this test method.  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method can be used to locate the glass transition region and assign a glass transition temperature of amorphous and semi-crystalline materials.  
5.2 Dynamic mechanical analyzers monitor changes in the viscoelastic properties of a material as a function of temperature and frequency, providing a means to quantify these changes. In ideal cases, the temperature of the onset of the decrease in storage modulus marks the glass transition.  
5.3 A glass transition temperature (Tg) is useful in characterizing many important physical attributes of thermoplastic, thermosets, and semi-crystalline materials including their thermal history, processing conditions, physical stability, progress of chemical reactions, degree of cure, and both mechanical and electrical behavior. Tg may be determined by a variety of techniques and may vary in accordance with the technique.  
5.4 This test method is useful for quality control, specification acceptance, and research.
SCOPE
1.1 This test method covers the assignment of a glass transition temperature (Tg) of materials using dynamic mechanical analyzers.  
1.2 This test method is applicable to thermoplastic polymers, thermoset polymers, and partially crystalline materials which are thermally stable in the glass transition region.  
1.3 The applicable range of temperatures for this test method is dependent upon the instrumentation used, but, in order to encompass all materials, the minimum temperature should be about −150°C.  
1.4 This test method is intended for materials having an elastic modulus in the range of 0.5 MPa to 100 GPa.  
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.6 This standard is similar to IEC 61006 except that standard uses the peak temperature of the loss modulus peak as the glass transition temperature while this standard uses the extrapolated onset temperature of the storage modulus change.  
1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Differing temperature rates-of-change may be required for different measurements (for example, Test Method E698). Temperature calibration changes as a function of temperature rate-of-change. The use of the known thermal lag of an apparatus may be used to adjust the temperature calibration of the apparatus obtained at one temperature rate-of-change with that at another required for a given applications. This adjustment procedure for temperature calibration is described in 8.1.  
5.2 This test method may be used in research, quality assurance, and specification acceptance.
SCOPE
1.1 This test method addresses the dependence of temperature calibration on the temperature rate-of-change. This test method describes the determination of the thermal lag of thermal analysis apparatus and its application to the modification of the temperature calibration for that apparatus obtained at alternative linear temperature rates-of-change.  
1.2 This test method is applicable, but not limited to, the temperature calibration of differential thermal analyzers (DTAs), differential scanning calorimeters (DSCs), thermogravimetric analyzers (TGAs), thermomechanical analyzers (TMAs), and dynamic mechanical analyzers (DMAs).  
1.3 The values stated in SI units are to be regarded as the standard. No other units of measurement are included in this standard.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 This test method may be used to validate the performance of a specific TGA apparatus.  
5.2 This test method may be used to validate the performance of a specific method based upon a TGA mass loss or residue measurement.  
5.3 This test method may be used to determine the repeatability of a specific apparatus, operator or laboratory.  
5.4 This test method may be used for specification and regulatory compliance purposes.
SCOPE
1.1 This test method provides procedures for validating mass loss and residue measurements by thermogravimetric analyzers (TGA) and analytical methods based upon the measurement of mass loss or residue content. Performance parameters determined include mass loss and residue repeatability (precision), detection limit, quantitation limit, linearity, and bias.  
1.2 Validation of apparatus performance and analytical methods is requested or required for quality initiatives or where results may be used for legal purposes.  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 There is no ISO standard equivalent to this test method.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Thermal conductivity is a useful design parameter for the rate of heat transfer through a material.  
5.2 The results of this test method may be used for design purposes, service evaluation, manufacturing control, research and development, and hazard evaluation. (See Practice E1231.)
SCOPE
1.1 This test method describes the determination of thermal conductivity of homogeneous, non-porous solid materials in the range of 0.10 W/(K • m) to 1.0 W/(K • m) by modulated temperature differential scanning calorimeter. This range includes many polymeric, glass, and ceramic materials. Thermal diffusivity, which is related to thermal conductivity through specific heat capacity and density, may also be derived. Thermal conductivity and diffusivity can be determined at one or more temperatures over the range of 0°C to 90°C.  
1.2 The values stated in SI units are to be regarded as standard. The values given in parentheses are mathematical conversions to inch-pound units that are provided for information only and are not considered standard.  
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health and environmental practices and determine the applicability of regulatory limitations prior to use.  
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Thermogravimetry provides a rapid method for the determination of the temperature-decomposition profile of a material.  
5.2 This practice is useful for quality control, specification acceptance, and research.  
5.3 This test method is intended to provide an accelerated thermal endurance estimation in a fraction of the time require for oven-aging tests. The primary product of this test method is the thermal index (temperature) for a selected estimated thermal endurance (time) as derived from material decomposition.  
5.4 Alternatively, the estimated thermal endurance (time) of a material may be estimated from a selected thermal index (temperature).  
5.5 Additionally, the estimated thermal endurance of a material at selected failure time and temperature may be estimated when compared to a reference value for thermal endurance and thermal index obtained from electrical or mechanical oven aging tests.  
5.6 This practice shall not be used for product lifetime predications unless a correlation between test results and actual lifetime has been demonstrated. In many cases, multiple mechanisms occur during the decomposition of a material, with one mechanism dominating over one temperature range, and a different mechanism dominating in a different temperature range. Users of this practice are cautioned to demonstrate for their system that any temperature extrapolations are technically sound.
SCOPE
1.1 This practice describes the determination of thermal endurance, thermal index, and relative thermal index for organic materials using the Arrhenius activation energy generated by thermogravimetry.  
1.2 This practice is generally applicable to materials with a well-defined thermal decomposition profile, namely a smooth, continuous mass change.  
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.4 There is no ISO standard equivalent to this practice.  
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.  
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

SIGNIFICANCE AND USE
5.1 Thermomechanical analyzers are employed in their various modes of operation (penetration, expansion, flexure, etc.) to characterize a wide range of materials. In most cases, the value to be assigned in thermomechanical measurements is the temperature of the transition (or event) under study. Therefore, the temperature axis (abscissa) of all TMA thermal curves must be accurately calibrated either by direct reading of a temperature sensor or by adjusting the programmer temperature to match the actual temperature over the temperature range of interest.
SCOPE
1.1 This test method describes the temperature calibration of thermomechanical analyzers from −50 to 1500°C. (See Note 1.)  
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 This standard is similar to ISO 11359–1 but addresses a larger temperature range and utilizes additional calibration materials.  
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. Specific precautionary statements are given in Section 7 and Note 11.

SIGNIFICANCE AND USE
5.1 The glass transition is dependent on the thermal history of the material to be tested. For amorphous and semicrystalline materials the assignment of the glass transition temperature may lead to important information about thermal history, processing conditions, stability, progress of chemical reactions, and mechanical and electrical behavior.  
5.2 Thermomechanical analysis provides a rapid means of detecting changes in hardness or linear expansion associated with the glass transition.  
5.3 This test method is useful for research and development, quality control, and specification acceptance.
SCOPE
1.1 This test method describes procedures for the assignment of the glass transition temperature of materials on heating using thermomechanical measurements under compression experimental conditions.  
1.2 This test method is applicable to amorphous or to partially crystalline materials that are sufficiently rigid below the glass transition to inhibit indentation by the sensing probe.  
1.3 The normal operating temperature range is from − 100 to 600°C. This temperature range may be extended depending upon the instrumentation used.  
1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.5 This test method is related to ISO 11359-2. ISO 11359-2 additionally covers the determination of coefficient of linear thermal expansion not covered by this test method. This test method is related to IEC 61006 but uses a slower heating rate.  
1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. Specific precautionary statements are given in Section 7.