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This document specifies a method for appraising the behaviour of cable insulation subjected to an electric arc initiated and maintained by a contaminating fluid. This document is intended to be used together with EN 3475-100. The primary aim of this test is: - to produce, in a controlled fashion, continuous failure effects, which are representative of those, which can occur in service when a typical cable bundle is damaged and subjected to aqueous fluid contamination such that electrical arcing occurs between cables; and - to examine the aptitude of the insulation to track, to propagate electric arc to the electrical origin. Originally defined for 115 VAC network, this test also proposes conditions for 230 VAC network. However, for 230 VAC test condition only, the test EN 3475-605 can overrule and be applied as test governance as it has been demonstrated that test EN 3475-605 is more stringent, repeatable and reproductible compared to EN 3475-604 and EN 3475-603. Six levels of prospective fault current have been specified for concerned cable sizes (see Clause 8). It is agreed that larger sizes need not be assessed since the short-circuit phenomenon becomes dominant at low line impedances. Unless otherwise specified in the technical/product standard, sizes 002, 006 and 020 cable are assessed.

 

This document describes a method for preparing asphalt blocks intended for testing of joint sealants according to prEN 13880-7 and EN 13880-9.

 

This document specifies test methods for the determination of the percentage of defective particles and of the microstructure of metallic blast-cleaning abrasives. This is one of a number of parts of ISO 11125 dealing with the sampling and testing of metallic abrasives for blast-cleaning. The types of metallic abrasive and requirements on each are contained in the various parts of ISO 11124. The ISO 11124 and ISO 11125 series have been drafted as a coherent set of International Standards on metallic blast-cleaning abrasives. Information on all parts of both series is given in Annex A.

 

 

 

This International Standard specifies ways in which rare earths can be traced as they move through the supply chain between the separated products to rare earth permanent magnets, or otherwise further processed. This standard complements ISO 23664. The documented traceability information will assist purchasers, suppliers, and users of rare earth permanent magnets to identify parties in the supply chain who have processed a given shipment of rare earth material, the location of that rare earth material as it passes between supply chain nodes. Supply chain actors and end users can use this information to check the validity of any claims made on the rare earth permanent magnets concerning sustainability, environmental impact, or recycled material content.

 

 

This document defines a method of determining bulk density of solid recovered fuels by the use of a standard measuring container. This method is applicable to all SRFs with a nominal top size of particle less than 1/3 of the container diameter specified in this document.

 

This document specifies methods for measuring and evaluating the performance of CO2 capture connected to a CO2 intensive plant, and which separate CO2 from the CO2 intensive plant exhaust gas in preparation for subsequent transportation and geological storage. In particular, it provides a common methodology to calculate key performance indicators for the CO2 capture plant, requiring the definition of the boundaries of a typical system and the measurements of parameters needed to determine the KPIs. This document covers the CO2 capture plant capturing CO2 from CO2 containing exhaust gas” connected to CO2 intensive plants. The connection of a CO2-capture plant to a CO2-intensive plant is anticipated to have negligible impact on the product quality or the quantities produced by the CO2-intensive plant. This is in contrast with the integration of CO2-capture plants with power plants which usually results in a reduction of the power plant output. For the CO2-intensive industry it is important that product quality remains the same after connection of the CO2-capture plant, in order for the industry to continue to meet customer requirements. The CO2 capture technologies covered by this document are able to operate without interfering with the operations of the CO2 intensive plant. Frequently used CO2 capture technologies are chemical absorption (e.g., liquid amine) and solid adsorption (e.g., Pressure Swing Adsorption (PSA), Temperature Swing Adsorption (TSA)). Other CO2 capture concepts are membranes, cryogenic and other capture technologies. The CO2 capture plant can be installed for treatment of the full volume of exhaust gas from the CO2 intensive plant or a fraction of the total (i.e. a slipstream). Captured CO2 is then conditioned, e.g. dried and compressed or liquefied, as determined by the conditions needed for transportation and storage. The transportation can be either through a pipeline or through an intermediate storage facility waiting for shipment; either by tanker car, train, or ship. The KPIs considered in this document are the following: The calculations are based on measurements at the boundary of the CO2 capture plant, particularly of energy and other utilities consumption. The system includes interfaces between the CO2 capture plant and the CO2 intensive plant. This document includes the following items: This document does not provide guidelines for benchmarking, comparing, or assessing KPIs of different technologies or different CO2 capture projects.

 

 

 

This document specifies common requirements for transportable liquid oxygen systems and specific requirements for base units. Base units are used as a store for liquid oxygen for recharging portable units. They may also, if fitted with a flow outlet and flow selector, be used as a source for the supply of oxygen direct to the patient.

 

This document specifies requirements for portable units which are part of a transportable liquid oxygen system. These are used as a supply source for oxygen therapy in home-care and in health-care facilities. Portable units are intended to be carried by patients whilst moving around and during their off-site activities and can be refilled from a base unit through a transfilling connector. Portable units are used without professional supervision.

 

This part of ISO/IEC 19770 provides This part of ISO/IEC 19770 is applicable to all types of organizations (e.g., commercial enterprises, government agencies, and non-profit organizations).

 

This document specifies requirements and provides recommendations for the pre-examination phase of cell free DNA (cfDNA) from body fluid specimens other than blood, including but not limited to the collection, handling, storage, transport, processing and documentation of human body fluids, such as urine, pleural effusions, ascites, cerebrospinal fluid (CSF), and saliva, intended for cfDNA examination. Processing includes multiple steps, such as centrifugation for specimen purification and isolation of cfDNA. This document is applicable to medical laboratories, health institutions including facilities collecting and handling specimens, laboratory customers, in vitro diagnostic examination developers and manufacturers, biobanks, institutions and organizations performing biomedical research, and regulatory authorities. Dedicated measures that need to be taken for cytohistological analysis of body fluid derived nucleated cells are not described in this document, neither are measures for preserving and handling of pathogens, and other bacterial or whole microbiome DNA in body fluids described. Different dedicated measures need to be taken for preserving circulating cell free DNA (ccfDNA) from blood. These are not described in this document, but are covered in ISO 20186-3.

 

 

This document contains simulation software for the MPEG-H 3D audio standard as defined in ISO/IEC 23008-3.

 

ISO 11431:2002 specifies a method for the determination of the adhesion/cohesion properties of sealants after cyclic exposure to heat and artificial light followed by a period of exposure to water at a defined temperature.

 

This international standard defines a method of determining bulk density of solid recovered fuels by the use of a standard measuring container.

 

This document specifies requirements and provides recommendations for the pre-examination phase of cell free DNA (cfDNA) from body fluid specimens other than blood, including but not limited to the collection, handling, storage, transport, processing and documentation of human body fluids, such as urine, cerebrospinal fluid (CSF), pleural effusions and saliva, intended for cfDNA examination. Processing includes multiple steps, such as centrifugation for specimen cleaning and isolation of cfDNA. This document is applicable to molecular in vitro diagnostic examinations performed by medical laboratories. It is also intended to be used by health institutions including facilities collecting and handling specimen, laboratory customers, in vitro diagnostics developers and manufacturers, biobanks, institutions and commercial organizations performing biomedical research, and regulatory authorities. Dedicated measures that need to be taken for cytohistological analysis of body fluid derived nucleated cells are not described in this document. Neither are measures for preserving and handling of pathogens, and other bacterial or whole microbiome DNA in body fluids described. Different dedicated measures need to be taken for preserving circulating cell free DNA (ccfDNA) from blood. These are not described in this document, but are covered in ISO 20186-3. NOTE International, national or regional regulations or requirements can also apply to specific topics covered in this document.