This document specifies methods for:
—    determining the composition of a calibration gas mixture by comparison with appropriate reference gas mixtures;
—    calculating the uncertainty of the composition of a calibration gas mixture in relation to the known uncertainty of the composition of the reference gas mixtures with which it was compared;
—    checking the composition attributed to a calibration gas mixture by comparison with appropriate reference gas mixtures;
—    consistency testing and outlier search in suites of calibration gas mixtures of closely related composition.
NOTE 1    In principle, the method described in this document is also applicable to the analysis of (largely) unknown samples instead of prospective calibration gas mixtures (i.e. gas mixtures which are intended for use as calibration gas mixtures). Such applications, however, need appropriate care and consideration of additional uncertainty components, for example, concerning the effect of matrix differences between the reference gases used for calibration and the analysed sample.
NOTE 2    Comparison methods based on one- and two-point calibration are described in ISO 12963.

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This document specifies methods for:
—    determining the composition of a calibration gas mixture by comparison with appropriate reference gas mixtures;
—    calculating the uncertainty of the composition of a calibration gas mixture in relation to the known uncertainty of the composition of the reference gas mixtures with which it was compared;
—    checking the composition attributed to a calibration gas mixture by comparison with appropriate reference gas mixtures;
—    consistency testing and outlier search in suites of calibration gas mixtures of closely related composition.
NOTE 1    In principle, the method described in this document is also applicable to the analysis of (largely) unknown samples instead of prospective calibration gas mixtures (i.e. gas mixtures which are intended for use as calibration gas mixtures). Such applications, however, need appropriate care and consideration of additional uncertainty components, for example, concerning the effect of matrix differences between the reference gases used for calibration and the analysed sample.
NOTE 2    Comparison methods based on one- and two-point calibration are described in ISO 12963.

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This document gives general information on the key steps for the preparation of candidate matrix reference materials (RMs) including the material specification, sourcing and selection of bulk material, and the processing of the material, which are important steps for the production of matrix RMs. The document provides information on the preparation of candidate RMs for laboratory staff who prepare and use matrix materials for their specific applications. This document can also be used by reference material producers (RMPs) as an information source for the preparation of the RMs that they produce. This document also offers examples of specific case studies covering the preparation of matrix RMs in different fields of application (see Annexes A to F). These are not complete "production manuals" but highlight key considerations for the preparation steps of RMs.

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This document describes good practice in using reference materials (RMs), and certified reference materials (CRMs) in particular, in measurement processes. These uses include: - the assessment of precision and trueness of measurement methods; - quality control; - assigning values to materials; - calibration; - establishing conventional scales. This document also relates key characteristics of various types of RMs to the different applications. The preparation of RMs for calibration is also part of the scope of ISO 17034 and ISO 33405. The treatment in this document is limited to the fundamentals of small-scale preparation of RMs and the value assignment, as used by laboratories to calibrate their equipment. Larger scale production of such RMs, with the possible aim of distribution, is beyond the scope of this document. This type of activity is covered in ISO 17034 and ISO 33405.

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This document notes the requirements of ISO 17034 and provides guidance on the implementation of ISO 17034 in the production of RMs having one or more assigned qualitative property values, for expressing uncertainties for qualitative property values, and for establishing traceability. NOTE The concepts of traceability and uncertainty address characteristics similar to those addressed by the concepts of traceability and measurement uncertainty as used in the metrology of quantitative properties. This document therefore does not describe aspects related to the production of RMs with quantitative property values. NOTE Annex A provides examples of types of RMs within the scope of this document.

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This document explains concepts and provides approaches to the following aspects of the production of reference materials (RMs): - the assessment of homogeneity; - the assessment of stability and the management of the risks associated with possible stability issues related to the properties of interest; - the characterization and value assignment of properties of an RM; - the evaluation of uncertainty for certified values; - the establishment of the metrological traceability of certified values. The guidance given supports the implementation of ISO 17034. Other approaches can also be used as long as the requirements of ISO 17034 are fulfilled. Brief guidance on the need for commutability assessment (6.11) is given in this document, but no technical details are provided. A brief introduction for the characterization of qualitative properties (9.6 to 9.8) is provided, together with brief guidance on sampling such materials for homogeneity tests (7.4.1.2). However, statistical methods for the assessment of the homogeneity and stability of RMs for qualitative properties are not covered. This document is also not applicable to multivariate quantities, such as spectral data. NOTE ISO 33406 gives more information on the production of RMs with one or more qualitative property values.

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SIGNIFICANCE AND USE
4.1 This test method was developed for the determination of bromine chloride in liquid chlorine. Bromide is a common contaminant in all salt sources that are used in the production of chlorine. This bromide content of the salt is converted into bromine chloride in the liquid chlorine product. This test method is sensitive enough to measure the levels of bromine chloride observed in normal production chlorine.
SCOPE
1.1 This test method uses high performance liquid chromatography (HPLC) to determine bromine chloride levels in liquid chlorine at the 10 μg/g (ppm) to 1400 μg/g (ppm) range.  
1.2 Review the current safety data sheet (SDS) for detailed information concerning toxicity, first aid procedures, and safety precautions.  
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 The following applies for the purposes of determining the conformance of the test results using this test method to applicable specifications, results shall be rounded off in accordance with the rounding-off method of Practice E29.  
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 hazard statements are given in Section 8.  
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.

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SIGNIFICANCE AND USE
4.1 This test method was developed for the determination of nitrogen trichloride in samples of carbon tetrachloride liquid taken from the compressor suction chiller bottoms of chlorine production plants and other places in the plants that may collect and concentrate nitrogen trichloride to levels that could explode. The test method was then modified to measure the lower levels of nitrogen trichloride observed in product liquid chlorine. This test method is sensitive enough to measure the levels of nitrogen trichloride observed in the normal production of liquid chlorine.  
4.2 This test method for nitrogen trichloride will require the dilution (100:1) of highly concentrated in-process samples to bring them within the working range of the analysis.
SCOPE
1.1 This test method uses high performance liquid chromatography (HPLC) to determine nitrogen trichloride levels in liquid chlorine at the 0.1 μg/g (ppm) to 600 μg/g (ppm) range. Solvent samples from chlorine production facilities containing very high concentrations of nitrogen trichloride may be analyzed by dilution with methanol.  
1.2 Review the current safety data sheet (SDS) for detailed information concerning toxicity, first aid procedures, and safety precautions.  
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 The following applies for the purposes of determining the conformance of the test results using this test method to applicable specifications, results shall be rounded off in accordance with the rounding-off method of Practice E29.  
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 hazard statements are given in Section 8.  
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.

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SIGNIFICANCE AND USE
5.1 This test method can be used to determine the acidity of catalysts and catalyst carriers by ammonia chemisorption for materials specifications, manufacturing control, and research and development in the evaluation of catalysts.
SCOPE
1.1 This test method covers the determination of acidity of catalysts and catalyst carriers by ammonia chemisorption. A volumetric measuring system is used to obtain the amount of chemisorbed ammonia.  
1.2 The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units 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.

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SCOPE
1.1 This terminology covers definitions of terms related to catalysts and catalysis.
Note 1: The Manual of Symbols and Terminology for Physicochemical Quantities and Units presents authoritative descriptions of many terms used in the field of catalysis.2  
1.2 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.

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This document is intended to help reference material producers (RMPs) in preparing clear and concise documentation to accompany a reference material (RM). It lists and explains mandatory, recommended and other categories of information to be considered in the preparation of product information sheets and RM certificates. This information can be used by RM users and other stakeholders in confirming the suitability of an RM or certified reference material (CRM). This document also contains the minimum requirements for a label attached to the container of an individual RM unit.

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SIGNIFICANCE AND USE
5.1 The BWC, as determined by this test method, is a measure of the ability of an activated carbon to adsorb and desorb butane from dry air under specified conditions. It is useful for quality control and evaluation of granular activated carbons that are used in applications where the adsorption of butane and desorption with dry air are of interest. The BWC can also provide a relative measure of the effectiveness of the tested activated carbons on other adsorbates.  
5.2 The butane activity and retentivity can also be determined under the conditions of the test. The butane activity is an indication of the micropore volume of the activated carbon sample. The butane retentivity is an indication of the pore structure of the activated carbon sample.
SCOPE
1.1 This test method covers the determination of the butane working capacity (BWC) of new granular activated carbon. The BWC is defined as the difference between the butane adsorbed at saturation and the butane retained per unit volume of carbon after a specified purge. The test method also produces a butane activity value that is defined as the total amount of butane adsorbed on the carbon sample and is expressed as a mass of butane per unit weight or volume of carbon.  
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. For a specific hazard statement, see 7.1.  
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.

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SIGNIFICANCE AND USE
5.1 The butane activity as determined by this test method is a measure of the ability of an activated carbon to adsorb butane from dry air under specified conditions. It is useful for the quality control and evaluation of granular activated carbons. The butane activity is an indication of the micropore volume of the activated carbon sample. This activity number does not necessarily provide an absolute or relative measure of the effectiveness of the tested carbon for other adsorbates or at other conditions of operation.  
5.2 The butane activity test can be used as a non-ozone depleting substitute for the carbon tetrachloride activity test in Test Method D3467. Fig. 1 shows an experimental correlation of activity values obtained using the two adsorbates.  
FIG. 1 Butane Versus Carbon Tetrachloride Correlation  
Note 1: This test has not been designed for use with powdered activated carbon, but it has been used successfully when the flow rate or time are adjusted or the sample volume is decreased to keep the pressure drop at an acceptable value.
SCOPE
1.1 This test method covers determination of the activation level of activated carbon. Butane activity (BA) is defined herein as the ratio (in percent) of the mass of butane adsorbed by an activated carbon sample to the mass of the sample, when the carbon is saturated with butane under the conditions listed in this test method.  
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. For a specific warning statement, see 7.1.  
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.

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SIGNIFICANCE AND USE
5.1 This test method has been found useful for the determination of the specific surface area of catalysts and catalyst carriers in the range from 0.05 m2/g to 10 m2/g for materials specification, manufacturing control, and research and development in the evaluation of catalysts. The determination of surface area of catalysts and catalyst carriers above 10 m2/g is addressed in Test Method D3663 – Surface Area of Catalyst and Catalyst Carriers – and is appropriate for most samples with specific surface areas above 1 m2/g.
SCOPE
1.1 This test method covers the determination of the specific surface area of catalysts and catalyst carriers in the range from 0.05 m2/g to 10 m2/g. A volumetric measuring system is used to obtain at least three data points which fall within the linear BET region.  
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 and health practices and determine the applicability of regulatory limitations prior to use.

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SIGNIFICANCE AND USE
5.1 This test method is to be used for measuring the vibratory packing density of formed particles that will not break up during sampling, filling, or vibrating of the measuring cylinder under test conditions.
SCOPE
1.1 This test method covers the determination of the vibratory packing density of formed catalyst and catalyst carriers. For the purpose of this test, catalyst particles are defined as extrudates, spheres, or formed pellets of 0.8-mm to 4.8-mm (1/32-in. to 3/16-in.) nominal diameter.  
1.2 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.  
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.

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SIGNIFICANCE AND USE
5.1 This test method is used for measuring the vibratory packing density of formed particles used in fixed bed reactors, driers, and so forth.
SCOPE
1.1 This test method covers the determination of the vibratory packing density of formed catalyst and catalyst carrier particles that will not break up significantly under test conditions. For the purpose of this test, catalyst particles are defined as extrudates, spheres or formed pellets greater than 4.8 mm.  
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.

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SIGNIFICANCE AND USE
4.1 The accuracy of many analytical measurements is dependent upon the manner in which the standard solutions are prepared and stored, and the accuracy with which they are standardized. Combining the methods recommended for the preparation and handling of such solutions into one practice eliminates the necessity for covering such details in all of the methods wherein the solutions are used.
SCOPE
1.1 This practice covers procedures for the preparation, standardization, and storage of the standard volumetric solutions and reagent testing solutions commonly used in chemical analysis.  
1.2 The information in this practice is arranged as follows:    
Sections  
Referenced Documents  
2  
Terminology  
3  
Significance and Use  
4  
Apparatus  
5  
Temperature effects  
6  
Measurements  
7  
Reagents  
8  
Concentration of solutions  
9  
Mixing of solutions  
10  
Storage of solutions  
11  
Preparation and standardization of solutions  
12  
Precision and Bias  
13  
Sodium hydroxide solution, 0.02 to 1.0 meq/mL (N)  
14 to 19  
Hydrochloric acid, 0.02 to 1.0 meq/mL (N)  
20 to 28  
Sulfuric acid, 0.02 to 1.0 meq/mL (N)  
29 to 33  
Hydrochloric acid, special 1 meq/mL (N)  
34 to 38  
Sulfuric acid, special 1 meq/mL (N)  
39 to 43  
Silver nitrate solution, 0.1 meq/mL (N)  
44 to 48  
Ammonium thiocyanate solution, 0.1 meq/mL (N)  
49 to 53  
Iodine solution, 0.1 meq/mL (N)  
54 to 58  
Sodium thiosulfate solution, 0.1 meq/mL (N)  
59 to 63  
Potassium permanganate solution, 0.1 meq/mL (N)  
64 to 68  
Potassium dichromate solution, 0.1 meq/mL(N)  
69 to 73  
Methanolic sodium hydroxide solution, 0.5 meq/mL (N)  
74 to 79  
Ceric sulfate solution, 0.1 meq/mL (N)  
80 to 84  
Acetous perchloric acid, 0.1 meq/mL (N)  
85 to 89  
Disodium ethylenediaminetetraacetate solution, 0.05 mol/L(M)  
90 to 94  
Standard ion solutions  
95  
Nonstandardized reagent solutions and indicator solutions  
96  
1.3 The values stated in SI units are to be regarded as standard. The values given in parentheses are for information only.  
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 warning statements are given throughout this practice. Consult current OSHA regulations, suppliers’ Safety Data Sheets, and local regulations for all materials used in this specification.  
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.

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This document specifies recommendations for single-phase certified reference materials (CRMs) used in electron probe microanalysis (EPMA). It also provides guidance on the use of CRMs for the microanalysis of flat, polished specimens. It does not cover organic or biological materials. This document supplements ISO 17034. A producer of CRM must also comply with ISO 17034. In case of conflict, ISO 17034 takes precedence.

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SIGNIFICANCE AND USE
5.1 This test method is used to determine the density expressed in g/mL for powdered or fine mesh carbon. Due to the nature of the small particles, the density of these carbon types cannot be measured using the same procedure as granular carbon.
SCOPE
1.1 This test method covers the determination of the mechanically tapped density of powdered and fine mesh activated carbon. For the purpose of this test method, “powdered carbon” is defined as having a mean particle diameter less than 45 µm, and “fine mesh carbon” is defined as having a particle size predominately between 80 and 325 U.S. Standard mesh.  
1.2 The values in SI units are to be regarded as standard. No other units of measure 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.

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SIGNIFICANCE AND USE
5.1 The particle size of fine mesh and powdered activated carbon is sometimes used to evaluate filter cake filtration rates and the filter penetration in filtering applications.  
5.2 The selection and handling of fine mesh or powdered activated carbon, and operation of processes using fine mesh or powdered activated carbon, requires the knowledge of the particle size.  
5.3 This test method is intended for single sieve testing only. For determination of particle size distribution of a sample, the test must be repeated using sieves with different openings.
Note 1: Relative humidity (RH) can affect the repeatability and accuracy of this test. Activated carbon not at equilibrium with the RH of the ambient air may lose or gain weight accordingly, dependent upon whether the carbon picks up or loses moisture.
SCOPE
1.1 This test method covers the determination of the particle size of powdered activated carbons using an air-jet sieve device. For purposes of this test method, powdered activated carbon is defined as activated carbon in particle sizes predominantly in a range of 80 mesh (0.180 mm) through 500 mesh (0.025 mm).  
1.2 The values stated in SI units are to be regarded as the standard. The inch-pound units given in parentheses are for information only.  
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.

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SIGNIFICANCE AND USE
4.1 The moisture content of activated carbon is often required to define and express its properties in relation to the net weight of the carbon.  
4.2 The moisture content of activated carbon packed in typical shipping containers will usually increase during transportation and storage. Users of activated carbon in applications where low moisture content is important should be aware of this effect.
SCOPE
1.1 These test methods provide three procedures for the determination of the moisture content of activated carbon. The procedures may also be used to dry samples required for other tests. The oven drying and moisture balance methods are used when water is the only volatile material present and is in significant quantities, and the activated carbon is not heat sensitive (some activated carbons can ignite spontaneously at temperatures as low as 150 °C). The xylene extraction method is used when a carbon is known or suspected to be heat sensitive or to contain miscible organic compounds instead of or in addition to water. The interferences posed by miscible inorganic compounds has not been determined. The oven drying method described in these test methods may be used as the reference for development of instrumental techniques for moisture determination in activated carbon.  
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.

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SIGNIFICANCE AND USE
5.1 This test method is intended to provide information concerning the ability of a powdered catalyst to resist particle size reduction during use in a fluidized environment.  
5.2 This test method is suitable for specification acceptance, manufacturing control, and research and development purposes.
SCOPE
1.1 This test method covers the determination of the relative attrition characteristics of FCC catalysts by means of air jet attrition. Other fine powder catalysts can be analyzed by this test method, but the precision of this test method has been determined only for FCC catalysts. It is applicable to spherically or irregularly shaped particles which range in size between 10 and 180 μm, have skeletal densities between 2.4 and 3.0 g/cm3 (2400 and 3000 kg/m3) (see IEEE/ASTM SI-10) and are insoluble in water. Particles less than 20 μm are considered fines. (See Terminology D3766.)  
1.2 Units—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.

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SIGNIFICANCE AND USE
5.1 The results of this test method give a conservative estimate of the performance of nuclear-grade activated carbon used in all nuclear power plant HVAC systems for the removal of radioiodine.
SCOPE
1.1 This test method is a very stringent procedure for establishing the capability of new and used activated carbon to remove radio-labeled methyl iodide from air and gas streams. The single test method described is for application to both new and used carbons, and should give test results comparable to those obtained from similar tests required and performed throughout the world. The conditions employed were selected to approximate operating or accident conditions of a nuclear reactor which would severely reduce the performance of activated carbons. Increasing the temperature at which this test is performed generally increases the removal efficiency of the carbon by increasing the rate of chemical and physical absorption and isotopic exchange, that is, increasing the kinetics of the radioiodine removal mechanisms. Decreasing the relative humidity of the test generally increases the efficiency of methyl iodide removal by activated carbon. The water vapor competes with the methyl iodide for adsorption sites on the carbon, and as the amount of water vapor decreases with lower specified relative humidities, the easier it is for the methyl iodide to be adsorbed. Therefore, this test method is a very stringent test of nuclear-grade activated carbon because of the low temperature and high relative humidity specified. This test method is recommended for the qualification of new carbons and the quantification of the degradation of used carbons.  
1.1.1 Guidance for testing new and used carbons using conditions different from this test method is offered in Annex A1.  
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.

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SIGNIFICANCE AND USE
5.1 This method compares the performance of granular or pelletized activated carbons used in odor control applications, such as sewage treatment plants, pump stations, etc. The method determines the relative breakthrough performance of activated carbon for removing hydrogen sulfide from a humidified gas stream. Other organic contaminants present in field operations may affect the H2S breakthrough capacity of the carbon; these are not addressed by this test. This test does not simulate actual conditions encountered in an odor control application, and is therefore meant only to compare the hydrogen sulfide breakthrough capacities of different carbons under the conditions of the laboratory test.  
5.2 This test does not duplicate conditions that an adsorber would encounter in practical service. The mass transfer zone in the 23 cm column used in this test is proportionally much larger than that in the typical bed used in industrial applications. This difference favors a carbon that functions more rapidly for removal of H2S over a carbon with slower kinetics. Also, the 1 % H2S challenge gas concentration used here engenders a significant temperature rise in the carbon bed. This effect may also differentiate between carbons in a way that is not reflected in the conditions of practical service.  
5.3 This standard as written is applicable only to granular and pelletized activated carbons with mean particle diameters less than 2.5 mm. Application of this standard to activated carbons with mean particle diameters (MPD) greater than 2.5 mm will require a larger diameter adsorption column. The ratio of column inside diameter to MPD should be greater than 10 in order to avoid wall effects. In these cases it is suggested that bed superficial velocity and contact time be held invariant at the conditions specified in this standard (4.77 cm/s and 4.8 s). Although not covered by this standard, data obtained from these tests may be reported as in paragraph 12 along with additional ...
SCOPE
1.1 This test method is intended to evaluate the performance of virgin, newly impregnated or in-service, granular or pelletized activated carbon for the removal of hydrogen sulfide from an air stream, under the laboratory test conditions described herein. A humidified air stream containing 1 % (by volume) hydrogen sulfide is passed through a carbon bed until 50 ppm breakthrough of H2S is observed. The H2S adsorption capacity of the carbon per unit volume at 99.5 % removal efficiency (g H2S/cm3 carbon) is then calculated. This test is not necessarily applicable to non-carbon adsorptive materials.  
1.2 This standard as written is applicable only to granular and pelletized activated carbons with mean particle diameters (MPD) less than 2.5 mm. See paragraph 5.3 if activated carbons with larger MPDs are to be tested.  
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.

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SIGNIFICANCE AND USE
4.1 This test method sets forth a procedure by which catalyst samples may be compared either on an interlaboratory or intralaboratory basis. It is anticipated that catalyst producers and users will find this test method to be of value.
SCOPE
1.1 This test method covers the determination of cobalt (expressed as the oxide) in fresh cobalt-molybdenum catalyst, in the range of 0.5 to 10 % cobalt oxide.  
1.2 Units—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.

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SIGNIFICANCE AND USE
5.1 This test method provides for the measurement of volume of pores that are in the range of catalytic importance and possibly for adsorption processes. This test method requires the use of mercury in order to perform the measurements.
SCOPE
1.1 This test method covers the determination of the total pore volume of catalysts and catalyst carriers, that is, the volume of pores having pore diameter between approximately 14 µm and 0.4 nm (4 Å).  
1.2 Units—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 material that can cause central nervous system, kidney, and liver damage. Mercury, or its vapor, may be hazardous to health and corrosive to materials. Caution should be taken when handling mercury and mercury containing products. See the applicable product Material Safety Data Sheet (MSDS) for details and EPA’s website—http://www.epa.gov/mercury/faq.htm—for additional information. Users should be aware that selling mercury or mercury containing products, or both, into your state or country may be prohibited by law.  
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 hazard statements are given in Section 8. Warning statements are given in 10.1.4, 10.1.7, and 10.1.11.  
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.

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SIGNIFICANCE AND USE
4.1 This test method is for measuring the apparent packing density of catalyst or catalyst carrier powders that are smaller than 0.8 mm in diameter.
SCOPE
1.1 This test method covers the determination of the apparent packing density of fine catalyst and catalyst carrier powders smaller than 0.8 mm in diameter.  
1.2 Units—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.

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SIGNIFICANCE AND USE
5.1 This test method is intended to provide information concerning the ability of a catalyst shape to retain physical integrity during use.
SCOPE
1.1 This test method covers determining the resistance of formed catalysts and catalyst carriers to compressive force and is applicable to regular catalyst shapes such as tablets and spheres. Other formed catalysts and catalyst carriers extrudates, granular materials, and other irregular shapes are specifically excluded.  
1.2 This test method determines the average crush strength in the range from 0 to 50 lbf (0 to 220 N). Some materials may have crush strengths above 50 lbf (220N); the test method is applicable to these materials, but the precision of the test is not known.  
1.3 Units—The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered 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.

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SIGNIFICANCE AND USE
4.1 This test method provides a means of determining the palladium content in fresh catalysts containing molecular sieves.  
4.2 This test method is not intended to cover samples containing precious metals other than palladium.
SCOPE
1.1 This test method covers the determination of palladium in molecular sieve-containing fresh catalysts with about 0.5 weight % of palladium.  
1.2 Units—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.

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SIGNIFICANCE AND USE
5.1 This guide provides an alternative way to measure the porosity of catalytic materials without the use of mercury porosimetry. It is useful for research and development as well as quality control purposes. (See Test Methods D4284 and D6761.)
SCOPE
1.1 This guide describes how to measure the pore volume of catalytic materials by water immersion with the excess water removed with a centrifuge. The measured pore volume is converted to the dry pore volume by using the loss on ignition (LOI) of the material. It is generally applicable to both powdered materials and particles greater than about 1 mm.  
1.2 Units—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.

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SIGNIFICANCE AND USE
5.1 The jet cup attrition test will provide an estimate of the relative attrition resistance of fluid catalytic cracking (FCC) catalyst, catalyst additives, and catalytic materials.  
5.2 The test is designed to simulate the attrition a catalyst or additive undergoes in a fluid catalytic cracking unit but at an accelerated rate.  
5.3 The data from this test can be used to rank catalyst according to attrition rate.  
5.4 The test requires a relatively small sample size of 5 g [0.175 oz] and a relatively short analysis time of 40 min. This test should be useful to quality control facilities that require fast turnaround time and research and development (R&D) facilities that have limited sample material.
SCOPE
1.1 The jet cup attrition test is applicable to fluid catalytic cracking (FCC) catalysts, catalyst additives, and catalytic materials.  
1.2 Applications for other powdered catalysts have been reported in the literature. The round robin test samples included two FCC catalysts and one powdered alumina.  
1.3 Units—The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system are not necessarily exact equivalents; therefore, to ensure conformance with the standard, each system shall be used independently of the other, and values from the two systems shall not be combined.  
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.

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SIGNIFICANCE AND USE
5.1 This guide is intended to determine meso- and macropore volume which affects heavy oil cracking performance of a catalyst. The information is useful for materials specification, manufacturing control, and research and development in the evaluation of catalytic materials.  
5.2 It has been reported in literature the existence of a correlation between the pore volume obtained from this guide and that from Test Method D4284.3
SCOPE
1.1 This guide measures pore volume of powdered catalysts and catalyst carriers by titration with water. The water does not react with material. The range of pore volume is 0.25 mL/g to 0.46 mL/g.  
1.2 This guide is suitable for fine catalysts such as fluid catalytic cracking (FCC) catalysts (fresh or equilibrium), catalyst additives and spray dried catalyst carriers or finished catalysts, or a combination thereof, and is typically applicable to powders with the majority of particles (above 90 %) in the distribution range between 20 and 150 µm equivalent spherical diameter (determined by Test Method D4464) and with an average particle size between 60 and 100 µm.
Note 1: This technique is capable of measuring particles below and above this range (for example, from 1 to 300 µm) but no precision data is available.  
1.3 Units—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.

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SIGNIFICANCE AND USE
4.1 Three forces can mechanically degrade a granular activated carbon: impact, crushing, and attrition. Of these three, attrition, or abrasion, is the most common cause of dust formation in actual service. Published test procedures to determine the “hardness” of activated carbons produce results that in general cannot be correlated with field experience. For example, the ball-pan hardness test applies all three forces to the sample in a variable manner determined by the size, shape, and density of the particles. The “stirring bar” abrasion test measures attrition so long as the particle size is smaller than 12 mesh. There is some evidence, however, that the results of this test method are influenced by particle geometry. The procedure set forth in this guide measures the effect of friction forces between vibrating or slowly moving particles during the test and may be only slightly dependent on particle size, shape, and density effects.
SCOPE
1.1 This guide presents a procedure for evaluating the resistance to dusting attrition of granular activated carbons. For the purpose of this guide, the dust attrition coefficient, DA, is defined as the weight (or calculated volume) of dust per unit time, collected on a preweighed filter, in a given vibrating device during a designated time per unit weight of carbon. The initial dust content of the sample may also be determined. Granular activated carbon is defined as a minimum of 90 % being larger than 80 mesh (0.18 mm) (see Test Methods D2867).  
1.2 The values stated in SI units are to be regarded as the standard. The inch-pound units given in parentheses are for information only.  
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.

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SIGNIFICANCE AND USE
4.1 This test method sets forth a procedure by which catalyst samples can be compared either on an interlaboratory or intralaboratory basis. It is anticipated that catalyst producers and users will find this method of value.
SCOPE
1.1 This test method covers the determination of nickel in fresh alumina-base catalysts and has been tested at nickel concentrations from 2.5 to 60 weight %, expressed as nickel oxide (NiO).  
1.2 Units—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.

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SIGNIFICANCE AND USE
5.1 Granular activated carbon (GAC) is commonly used to remove contaminants from water. However if not used properly, GAC can not only be expensive but can at times be ineffective. The development of engineering data for the design of full-scale adsorbers often requires time-consuming and expensive pilot plant studies. This rapid standard practice has been developed to predict adsorption in large-scale adsorbers based upon results from small column testing. In contrast to pilot plant studies, the small-scale column test presented in this practice does not allow for a running evaluation of factors that may affect GAC performance over time. Such factors may include, for example, an increased removal of target compounds by bacterial colonizing GAC3 or long-term fouling of GAC caused by inorganic compounds or background organic matter.4 Nevertheless, this practice offers more relevant operational data than isotherm testing without the principal drawbacks of pilot plant studies, namely time and expense; and unlike pilot plant studies, small-scale studies can be performed in a laboratory using water sampled from a remote location.  
5.2 This practice known as the rapid small-scale column test (RSSCT) uses empty bed contact time (EBCT) and hydraulic loading to describe the adsorption process. Mean carbon particle diameter is used to scale RSSCT results to predict the performance of a full-scale adsorber.  
5.3 This practice can be used to compare the effectiveness of different activated carbons for the removal of contaminants from a common water stream.
SCOPE
1.1 This practice covers a test method for the evaluation of granular activated carbon (GAC) for the adsorption of soluble pollutants from water. This practice can be used to estimate the operating capacities of virgin and reactivated granular activated carbons. The results obtained from the small-scale column testing can be used to predict the adsorption of target compounds on GAC in a large column or full-scale adsorber application.  
1.2 This practice can be applied to all types of water including synthetically contaminated water (prepared by spiking high-purity water with selected contaminants), potable waters, industrial wastewaters, sanitary wastes, and effluent waters.  
1.3 This practice is useful for the determination of breakthrough curves for specific contaminants in water, the determination of the lengths of the adsorbates mass transfer zones (MTZ), and the prediction of GAC usage rates for larger scale adsorbers.  
1.4 The following safety caveat applies to the procedure section, Section 10, of this practice: 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.

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SIGNIFICANCE AND USE
4.1 This test method sets forth a procedure by which catalyst samples can be compared either on an interlaboratory or intralaboratory basis. It is anticipated that catalyst producers and users will find this method of value.
SCOPE
1.1 This test method covers the determination of molybdenum in alumina-base catalysts and has been cooperatively tested at molybdenum concentrations from 8 to 18 weight %, expressed as MoO3. Any component of the catalyst other than molybdenum such as iron, tungsten, etc., which is capable of being oxidized by either ferric or ceric ions after being passed through a zinc-amalgam reductor column (Jones reductor) will interfere.  
1.2 Units—The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.  
1.3 Many catalysts that contain molybdenum also contain other metals, nickel for example, that may be regulated by the EPA. Go to the material safety data sheet for the catalyst material being analyzed. More information can be found at EPA.gov. Additional information on nickel containing catalysts can be found in Test Method D4481.  
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.

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SIGNIFICANCE AND USE
5.1 The test method has two main functions: first, it provides data useful for establishing the pore size distribution of catalyst materials, which in turn may influence their performance; and second, it serves as a laboratory test which may be used to study porosity changes that may occur during the manufacture and evaluation of catalysts.
SCOPE
1.1 This test method covers the determination of nitrogen adsorption and desorption isotherms of catalysts and catalyst carriers at the boiling point of liquid nitrogen.2 A static volumetric measuring system is used to obtain sufficient equilibrium adsorption points on each branch of the isotherm to adequately define the adsorption and desorption branches of the isotherm. Thirty points evenly spread over the isotherm is considered to be the minimum number of points that will adequately define the isotherm.  
1.2 Units—The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units 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.

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SIGNIFICANCE AND USE
5.1 This guide is intended to provide information concerning the ability of formed catalysts or catalyst carriers to resist particle size reduction during use. It can be used by itself or in conjunction with other methods to assess catalytic material integrity, such as Test Methods D4058 and D7084.  
5.2 There are no known restrictions on sample geometry, as spheres, pellets, and hollow cylinders are suitable for testing.  
5.3 This guide, as written, is suitable for use for catalytic materials from about 1/8 in. to about 3/4 in. It can also be used for larger parts, but this requires using a larger diameter pipe.  
5.4 This guide is suitable for specification acceptance, manufacturing control, and research and development processes.
SCOPE
1.1 The resistance to breakage of formed catalysts, catalyst carriers, or catalyst pieces is determined by dropping a quantity of sample through a 25 ft length of 1 in. internal diameter pipe onto a steel plate.  
1.2 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.  
1.3 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.

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ABSTRACT
This test method establishes the standard procedure for determining the surface areas of catalyst and catalyst carriers that have Type II or IV nitrogen adsorption isotherms, and specified minimum area. A volumetric measuring system is used to obtain at least four data points which fit on the linear BET line. The surface area of a catalyst or catalyst carrier is determined by measuring the volume of nitrogen gas adsorbed at various low-pressure levels by the catalyst sample. Pressure differentials caused by introducing the catalyst surface area to a fixed volume of nitrogen in the test apparatus are measured and used to calculate BET surface area.
SCOPE
1.1 This test method covers the determination of surface areas of catalyst and catalyst carriers that have Type II or IV nitrogen adsorption isotherms, and at least 1 m2/g of area. A volumetric measuring system is used to obtain at least four data points which fit on the linear BET2 equation line.  
1.2 Units—The values stated in SI units are to be regarded as standard. The values given in parentheses after SI units 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.

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SIGNIFICANCE AND USE
4.1 This test method sets forth a procedure by which duplicate catalyst samples can be compared either on an interlaboratory or intralaboratory basis. It is anticipated that catalyst producers and users will find this test method of value.  
4.2 Discrimination of the samples for which this procedure is recommended must be exercised when considering carrier (support) materials that sorb appreciable quantities of hydrogen or could cause an alteration of the state of the catalyst during pretreatment, or both, (that is, sintering or metal occlusion). These materials must be identified by the user and experimented with to determine the most significant conditions of measurement.  
4.3 This test method provides a measure of the total hydrogen uptake (volume of hydrogen at STP, cm3/g of catalyst) without specifying the nature of the hydrogen-platinum interaction. Persons interested in using hydrogen uptake data to calculate percent platinum dispersion in a specific catalyst should be aware of carrier (support) interactions, spillover effects, and other phenomena related to the hydrogen uptake capabilities of the catalyst in question.
SCOPE
1.1 This test method covers the determination of the chemisorption of hydrogen at 298 K (25 °C) on supported platinum catalysts that have been reduced in flowing hydrogen at 723 K (450 °C). It incorporates a static volumetric vacuum technique at constant volume.  
1.2 The test method is intended for use on unused supported platinum on alumina catalysts of loadings greater than 0.3 weight %. Data on other supports and lower platinum loadings were not tested.  
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.

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SIGNIFICANCE AND USE
4.1 Zeolite Beta is a siliceous zeolite that can be crystallized with SiO2/Al2O3 ratio greater than 20. Zeolite Beta, upon modification to the H-cation form in a post-crystallization step, has been used in catalytic NOx reduction, isomerization of waxes, alkylation of aromatics, hydrocarbon adsorption from exhaust gas emission, etc.  
4.2 This X-ray procedure is designed to allow a reporting of the relative degree of crystallinity upon manufacture of zeolite Beta. The relative crystallinity of zeolite Beta number has proven useful in technology, research, and specifications.  
4.3 The Integrated Peak Area Method (Procedure A) is preferred over the Peak Height Method (Procedure B) since it calculates XRD intensity as a sum from several peaks rather than utilizing just one peak. Drastic changes in intensity of individual peaks in the XRD pattern of zeolite Beta can result from changes in distribution of electron density within the unit cell of the zeolite Beta. The electron density distribution is dependent upon the following factors:  
4.3.1 Extent of filling of pores with guest molecules and the nature of these guest molecules.  
4.3.2 Type of cations and extent of their presence (these cations may also affect the absorption of X rays by the zeolite Beta sample).  
4.3.3 In this XRD method, the guest molecule H2O completes the filling of the pores. Other guest molecule types may also be present, including one of numerous amines, diamines, and quaternary ammonium cations that can function as a template for crystallization of the zeolite Beta structure.  
4.3.4 Because of the factors mentioned in 4.3.1 – 4.3.3 that could vary the intensities of the XRD peaks in zeolite Beta, this XRD method will provide the best determination of relative crystallinity when the reference zeolite Beta and sample zeolite Beta have a similar history of preparation and composition.  
4.4 If crystalline phases other than zeolite Beta are present in the sample, their diffraction peaks...
SCOPE
1.1 This test method covers a procedure for determination of the relative crystallinity of zeolite Beta containing samples using selected peaks from the X-ray diffraction (XRD) pattern of the zeolite.  
1.2 The test method provides a number that is the ratio of intensity of a portion of the XRD pattern of the sample zeolite Beta to intensity of the corresponding portion of the pattern of a reference zeolite Beta. The intensity ratio, expressed as a percentage, is then labeled percent XRD relative crystallinity of zeolite Beta. This type of comparison is commonly used in zeolite technology and is often referred to as percent crystallinity.  
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.

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SIGNIFICANCE AND USE
4.1 This test method is for estimating the relative amount of gamma alumina in calcined catalyst or catalyst carrier samples, assuming that the X-ray powder diffraction peak occurring at about 67 °2θ is attributable to gamma alumina. Gamma alumina is defined as a transition alumina formed after heating in the range from 500 to 550 °C, and may include forms described in the literature as eta, chi, and gamma aluminas. Delta alumina has a diffraction peak in the same region, but is formed above 850 °C, a temperature to which most catalysts of this type are not heated. There are other possible components which may cause some interference, such as alpha-quartz and zeolite Y, as well as aluminum-containing spinels formed at elevated temperatures. If the presence of interfering material is suspected, the diffraction pattern should be examined in greater detail. More significant interference may be caused by the presence of large amounts of heavy metals or rare earths, which exhibit strong X-ray absorption and scattering. Comparisons between similar materials, therefore, may be more appropriate than those between widely varying materials.
SCOPE
1.1 This test method covers the determination of gamma alumina and related transition aluminas in catalysts and catalyst carriers containing silica and alumina by X-ray powder diffraction, using the diffracted intensity of the peak occurring at about 67 °2θ when copper Kα radiation is employed.  
1.2 Units—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.

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This document describes the classification, method of sample preparation, certification main rules and certificate content of the EURONORM-CRMs.
It also details the sample presentation of the various producers' organizations and the distributing sources.

  • Technical report
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This document describes the classification, method of sample preparation, certification main rules and certificate content of the EURONORM-CRMs.
It also details the sample presentation of the various producers' organizations and the distributing sources.

  • Technical report
    11 pages
    English language
    e-Library read for
    1 day

ABSTRACT
This standard covers the specifications for physical properties and performance requirements of virgin impregnated activated carbon to be used for the removal of gaseous radioiodine species from gas streams. The activated carbon furnished under this specification shall be virgin material. Each batch of impregnated activated carbon shall conform to the requirements for physical properties prescribed. The following test methods shall used to determine the physical properties and performance capability of the sample: apparent density; particle size distribution; ash content; moisture content; ignition temperature; ball-pan hardness; and pH.
SIGNIFICANCE AND USE
5.1 Activated carbons used in containment systems for nuclear reactors must be capable of functioning under both normal operating conditions and those conditions which may exist following a design basis accident (DBA). Adsorbent beds that are part of recirculatory systems inside containment may be exposed to the peak pressure, temperature, and steam content of a post-DBA condition.  
5.2 Carbon beds outside containment will be protected by fast-acting shutoff valves from the sudden rise in pressure, temperature, and humidity of the containment atmosphere which would exist following a DBA. However, some rise in temperature and humidity will be experienced even by beds outside containment if they are reconnected to containment after the initial pressure rise (due to escape of steam into the containment volume) has been reduced by containment coolers. The amount of radioactivity that can reach either type of adsorption system is conceivably quite high; hence, there is a possibility of a bed temperature rise due to decay heating. The gaseous radioactive contaminants of most interest are organic iodides. In this test, CH3I is used to typify the performance of the carbon on organic iodine compounds in general. The test described here provide a reasonable picture of the effectiveness of an activated carbon for organic iodides under normal and post-DBA conditions. The equipment and methods described can be used, with discretion, for similar tests at different gas flow conditions and, to some extent, on different gaseous radioactive contaminants and other adsorbents.
SCOPE
1.1 This standard covers the specifications for physical properties and performance requirements of virgin impregnated activated carbon to be used for the removal of gaseous radioiodine species from gas streams.  
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 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.

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SIGNIFICANCE AND USE
5.1 In certain applications, the ash, color, conductivity, or pH of the finished activated carbon product may be influenced by the quantity of water solubles it contains. This water solubles test provides a relative indication of the quantity of soluble materials that may be extracted from various activated carbons.
SCOPE
1.1 This test method covers the determination of the water-soluble content of (unused) granular and powdered activated carbons. Water solubles are materials that can be extracted by distilled water under reflux conditions and are expressed as a percentage of dry carbon weight.  
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.

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SIGNIFICANCE AND USE
4.1 This test method is considered to be a measure of the propensity of a catalyst to produce fines in the course of transportation, handling, and use. However, there is no absolute level of acceptability. The values obtained are significant principally in relation to values for other materials (or other samples of the same material) of comparable size.
SCOPE
1.1 This test method covers the determination of the attrition and abrasion resistance of catalysts and catalyst carriers. It is applicable to tablets, extrudate, spheres, and irregularly shaped particles larger than about 1/16 in. (1.6 mm) and smaller than about 3/4 in. (19 mm). The materials used in developing the method exhibited losses on attrition less than 7 %; however, the method should be applicable to materials giving much higher attritions.  
1.2 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI 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.

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SIGNIFICANCE AND USE
4.1 The determination of contact pH can be used as a simple and fast measurement that can allow activated carbon producers and users to have a standard method for assessing the effect various carbons will have on the initial pH of the water in contact with the carbon. It has been determined that there is a bias between this method and Test Method D3838; they are not equivalent.
SCOPE
1.1 This method is to be used in the determination of the pH of water on initial contact with activated carbon. This test method is not meant as a replacement for Test Method D3838 and may give a different value.  
1.2 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.  
1.3 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.

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  • Standard
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