71.060.01 - Inorganic chemicals in general
ICS 71.060.01 Details
Inorganic chemicals in general
Anorganische Verbindungen im allgemeinen
Chimie minerale en general
Anorganske kemikalije na splošno
General Information
Frequently Asked Questions
ICS 71.060.01 is a classification code in the International Classification for Standards (ICS) system. It covers "Inorganic chemicals in general". The ICS is a hierarchical classification system used to organize international, regional, and national standards, facilitating the search and identification of standards across different fields.
There are 41 standards classified under ICS 71.060.01 (Inorganic chemicals in general). These standards are published by international and regional standardization bodies including ISO, IEC, CEN, CENELEC, and ETSI.
The International Classification for Standards (ICS) is a hierarchical classification system maintained by ISO to organize standards and related documents. It uses a three-level structure with field (2 digits), group (3 digits), and sub-group (2 digits) codes. The ICS helps users find standards by subject area and enables statistical analysis of standards development activities.
This document specifies a methodology applying poultices for the desalination of porous substrate constituting cultural heritage. The desalination methodology can be applied:
- to salt-loaded porous inorganic materials affected by salt weathering, and/or
- to allow conservation treatments incompatible with soluble salt(s) contamination, or
- to prevent salt damage where contamination is known to be present.
In all cases the desalination aims to decrease the salt content.
Furthermore, this document gives the fundamental requirements for the desalination operation and guidelines for the choice of the most appropriate poultice components according to the characteristics of the substrate and types/quantities of salt(s) present in order to optimize the desalination process.
- Standard30 pagesEnglish languagee-Library read for1 day
This document specifies a methodology applying poultices for the desalination of porous substrate constituting cultural heritage. The desalination methodology can be applied:
- to salt-loaded porous inorganic materials affected by salt weathering, and/or
- to allow conservation treatments incompatible with soluble salt(s) contamination, or
- to prevent salt damage where contamination is known to be present.
In all cases the desalination aims to decrease the salt content.
Furthermore, this document gives the fundamental requirements for the desalination operation and guidelines for the choice of the most appropriate poultice components according to the characteristics of the substrate and types/quantities of salt(s) present in order to optimize the desalination process.
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SIGNIFICANCE AND USE
4.1 This guide is intended to help analysts in the semiconductor industry. Examples of the usefulness of anion monitoring include: (1) determining when ion-exchange resin beds (in water-purification systems) need to be regenerated, and (2) ensuring that anion levels are low enough to allow the water to be used for the manufacture of semiconductor devices.
4.2 To ensure that the anions are indeed at low-ppt levels, it is recommended to check the conductivity of a subsample before proceeding with Section 5 of this guide. This check does not need to be exact; its purpose is simply to let the analyst know if the conductivity is higher than that of the highest-level standard solution being tested. Any high reading signifies that the sample, if analyzed, might contaminate the instrument.
SCOPE
1.1 This guide applies to ultrapure water that is thought to contain low ppt (parts-per-trillion, weight/weight) levels of anionic contaminants (for example, bromide, chloride, fluoride, nitrate, nitrite, phosphate, and sulfate). To minimize carry-over problems between analyses, it is best to limit the concentration of any one contaminant to approximately 200 ppt (although this limit is only an approximation and may vary, depending on the user’s application).
1.2 This guide is intended to help analysts avoid contamination of ultrapure-water samples, since contamination control is the primary challenge when quantifying ppt-level anions in grab samples.
1.3 This guide does not include recommendations for collecting samples from the water source.
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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SCOPE
1.1 This standard covers terminology relating to industrial and specialty chemicals. It is intended to provide an understanding of terms commonly used in test methods, practices, and specifications throughout the industry.
Note 1: The boldface numbers following each definition refer to E15 standards in which the definition appears. Lightface numbers refer to the E15 subcommittee having jurisdiction.
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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SIGNIFICANCE AND USE
5.1 Representative samples of industrial chemicals are required for the determination of chemical and physical properties which are used to establish standard volumes, prices, and compliance with commercial and regulatory specifications.
5.2 The objective of sampling is to obtain a small portion (spot sample) of material from a selected area within a container which is representative of the material in the area or, in the case of running or all-level samples, a sample whose composition is representative of the total material in the container. A series of spot samples may be combined to create a representative sample.
5.3 Manual and Automatic Sampling Considerations—The selection of manual or automatic sampling devices is part of establishing a sampling plan applied under all conditions within the scope of this practice provided that the proper sampling procedures are followed. Both types of sampling are commonly used for liquid, solid, and slurry sampling and require adherence to the following:
5.3.1 An adequate frequency of sampling must be selected.
5.3.2 The equipment to support manual or automatic sampling systems may be obtained commercially, fabricated from the designs presented in this practice, or constructed as needed to satisfy process design or other specific requirements.
5.3.3 The sampling equipment must be maintained on a regular basis, and the sampling plan adopted must be strictly followed.
SCOPE
1.1 This practice covers procedures for sampling several classes of industrial chemicals. It also includes recommendations for determining the number and location of such samples, to ensure their being representative of the lot in accordance with accepted probability sampling principles.
1.2 Although this practice describes specific procedures for sampling various liquids, solids, and slurries, in bulk or in packages, these recommendations only outline the principles to be observed. They should not take precedence over specific sampling instructions contained in other ASTM product or method standards.
1.3 These procedures are covered as follows:
Sections
Statistical Considerations
7 – 11
Simple Liquids
12 – 27
Solids
28 – 35
Slurries
36 – 41
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 Sections 6, 19, 20, 30, 34 and 37.
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 Zeolites Y and X, particularly for catalyst and adsorbent applications, are a major article of manufacture and commerce. Catalysts and adsorbents comprising these zeolites in various forms plus binder and other components have likewise become important. Y-based catalysts are used for fluid catalytic cracking (FCC) and hydrocracking of petroleum, while X-based adsorbents are used for desiccation, sulfur compound removal, and air separation.
4.2 This X-ray procedure is designed to monitor these Y and X zeolites and catalysts and adsorbents, providing a number more or less closely related to percent zeolite in the sample. This number has proven useful in technology, research, and specifications.
4.3 Drastic changes in intensity of individual peaks in the XRD patterns of Y and X can result from changes of distribution of electron density within the unit cell of the zeolite. The electron density distribution is dependent upon the extent of filling of pores in the zeolite with guest molecules, and on the nature of the guest molecules. In this XRD method, the guest molecule H2O completely fills the pores. Intensity changes may also result if some or all of the cations in Y and X are exchanged by other cations.
4.3.1 Because of the factors mentioned in 4.3 that could vary the intensities of the XRD peaks, this XRD method will provide the best determination of relative crystallinity when the reference and sample have a similar history of preparation and composition.
4.4 Corrections are possible that can make this XRD method accurate for measuring percent zeolite in many specific situations. These corrections are well known to those skilled in X-ray diffraction. It is not practical to specify those corrections here.
SCOPE
1.1 This test method covers the determination of relative X-ray diffraction intensities of zeolites having the faujasite crystal structure, including synthetic Y and X zeolites, their modifications such as the various cation exchange forms, and the dealuminized, decationated, and ultrastable forms of Y. These zeolites have cubic symmetry with a unit cell parameter usually within the limits of 24.2 and 25.0 Å (2.42 and 2.50 nm).
1.2 The samples include zeolite preparations in the various forms, and catalysts and adsorbents containing these zeolites.
1.3 The term “intensity of an X-ray powder diffraction (XRD) peak” is the “integral intensity,” either the area of counts under the peak or the product of the peak height and the peak width.
1.4 This test method provides a number that is the ratio of intensity of portions of the XRD pattern of the sample to intensity of the corresponding portion of the pattern of a reference zeolite, NaY. (Laboratories may use a modified Y or X, for example, REY as a secondary standard.) The intensity ratio, expressed as a percentage, is then labeled “% XRD intensity/NaY.”
1.5 Under certain conditions such a ratio is the percent zeolite in the sample. These conditions include:
1.5.1 The zeolite in the sample is the same as the reference zeolite.
1.5.2 The absorption for the X-rays used is the same for the zeolite and the nonzeolite portions of the sample.
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.
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SIGNIFICANCE AND USE
4.1 The purity of water is relative and is usually characterized by the limits of impurities found in the water as well as by the methods used to prepare and handle the water. Section 7 mentions the suitable methods for water preparation.
SCOPE
1.1 This guide is intended to describe the chemical and biological characteristics of water to be used whenever critical purity is essential to the use intended in laboratory bio-applications, for example, clinical, pharmaceutical, and biomedical. The importance of such a reagent is often underestimated despite the impact that it can have.
1.2 This guide is not intended to be used as a reference in preparing water for injectables. Generally, the appropriate use of this guide may include experiments involving tissue culture, chromatography, mass spectrometry, polymerase chain reaction (PCR), deoxyribonucleic acid (DNA) sequencing, DNA hybridization, electrophoresis, molecular biology or analyses where molecular concentrations of impurities may be important.
1.3 For all the other applications linked to an ASTM method and not bio-sensitive that require purified water, it is recommended that Specification D1193 or Guide D5127 be consulted.
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.
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SIGNIFICANCE AND USE
6.1 Test Method A is frequently used to test large systems and complex piping installations that can be filled with a trace gas. Helium is normally used. The test method is used to locate leaks but cannot be used to quantify except for approximation. Care must be taken to provide sufficient ventilation to prevent increasing the helium background at the test site. Results are limited by the helium background and the percentage of the leaking trace gas captured by the probe.
6.2 Test Method B is used to increase the concentration of trace gas coming through the leak by capturing it within an enclosure until the signal above the helium background can be detected. By introducing a calibrated leak into the same volume for a recorded time interval, leak rates can be measured.
SCOPE
1.1 This practice covers procedures for testing and locating the sources of gas leaking at the rate of 1 × 10 −7 Pa m3/s (1 × 10−8 Std cm3/s)3 or greater. The test may be conducted on any device or component across which a pressure differential of helium or other suitable tracer gas may be created, and on which the effluent side of the leak to be tested is accessible for probing with the mass spectrometer sampling probe.
1.2 Two test methods are described:
1.2.1 Test Method A—Direct probing, and
1.2.2 Test Method B—Accumulation.
1.3 Units—The values stated in either SI or std-cc/sec units are to be regarded separately as standard. The values stated in each system may not be exact equivalents: therefore, each system shall be used independently of the other. Combining values from the two systems may result in non-conformance with the 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 and health 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 test method is suitable for setting specification, for use as an internal quality control tool, and for use in development or research work on industrial aromatic hydrocarbons and related materials. In addition to the pure liquid chemicals for which expansion functions are known, it may also be used for liquids for which temperature expansion data are not available, or for impure liquid chemicals if certain limitations are observed. Information derived from this test can be used to describe the relationship between weight and volume.
SCOPE
1.1 This test method describes a simplified procedure for the measurement of density or relative density of pure liquid chemicals for which accurate temperature expansion functions are known. It is restricted to liquids having vapor pressures not exceeding 79 993 Pascal (0.800 bar, 600 mm Hg (0.789 atm) at the equilibration temperature, and having viscosities not exceeding 15 cSt at 20°C.
1.2 Means are provided for reporting results in the following units:
Density g/cm3 at 20°C
Density g/mL at 20°C
Relative density 20°C/4°C
Relative density 15.56°C/15.56°C
Note 1: This test method is based on the old definition of 1 L = 1.000028 dm3 (1 mL = 1.000028 cm3). In 1964 the General Conference on Weights and Measures withdrew this definition of the litre and declared that the word “litre” was a special name for the cubic decimetre, thus making 1 mL = 1 cm3 exactly.
Note 2: An alternative method for determining relative density of pure liquid chemicals is Test Method D4052.
1.3 In determining the conformance of the test results using this method to applicable specifications, results shall be rounded off in accordance with the rounding-off method of Practice E29.
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 hazard statements are given in Section 8, Hazards.
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.
WITHDRAWN RATIONALE
This test method described a simplified procedure for the measurement of density or relative density of pure liquid chemicals for which accurate temperature expansion functions are known. It is restricted to liquids having vapor pressures not exceeding 79 993 Pascal (0.800 bar, 600 mm Hg (0.789 atm) at the equilibration temperature, and having viscosities not exceeding 15 cSt at 20 °C.
Formerly under the jurisdiction of Committee D16 on Aromatic, Industrial, Specialty and Related Chemicals, this test method was withdrawn in August 2023. This standard is being withdrawn without replacement due to its limited use by industry.
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Specifies a method applicable to products in which the nickel content being determined exceeds 0,1 mg/kg. The principle of determination is based on dissolution of a test portion, formation of the coloured nickel furil -dioxime complex, extraction with chloroform and photometric measurement at a wavelength of about 435 nm.
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Describes a method applicable to products having cobalt contents equal to or greater than 0,1 mg/kg. The principle of determination is based on dissolution of a test portion, formation of the coloured cobalt 2-nitrose-1-naphtol complex, extraction with chloroform and photometric measurement at a wavelength of about 530 nm.
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Alkaline fusion of a test portion by sodium carbonate and subsequent neutralization by sulphuric acid. Measurement of the absorption of the complex formed by chromium and diphenylcarbazide at a wavelength of abour 540 nm after adding sodium azide for elimination of the colour caused by manganese.
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The principle consists in titration of the cloride ions with standard volumetric mercury(II) nitrate solution in presence of diphenylcarbazone as indicator until the colour of the solution matches the mauve of the standard end-point matching solution.
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Preliminary reduction of the iron(III) by hydroxylammonium chloride, if required, suppression of the interference of tin by oxalic acid. Formation of the coloured iron(III)-2,2'-dipyridyl complex in a buffered medium. Photometric measurement of the coloured complex at a wavelength of about 522 nm.
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The principle consists in removal of the boron by evaporation with methanol and separation of manganese and other metals from the residue, by extraction with chloroform, as their diethyldithiocarbamates. Wet destruction of the diethyldithiocarbamates with a sulphuric acid/ hydrogen peroxide mixture. Removal of any interfering iron by extraction as the thiocyanate. Formation of the coloured manganese formaldoxime complex in alkaline solution and photometric measurement at a wavelength of approximately 450 nm.
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