5.1 Reflective insulation, radiant barrier and vinyl stretch ceiling materials are evaluated in accordance with Test Method E84 to comply with building or mechanical code requirements. This practice describes, in detail, a specimen mounting procedure for reflective insulation, radiant barrier and vinyl stretch ceiling materials.5.2 The material shall be representative of the materials used in actual field installations.5.3 Specimen preparation and mounting procedures for materials not described in this practice shall be added as the information becomes available.5.4 The limitations for this procedure are those associated with Test Method E84.5.5 This practice shall not apply to rigid foam plastics with or without reflective facers.5.6 This practice shall not apply to site-fabricated stretch systems covered by Practice E2573.1.1 This practice describes a procedure for specimen preparation and mounting when testing reflective insulation, radiant barrier and vinyl stretch ceiling materials to assess flame spread and smoke development as surface burning characteristics using Test Method E84.1.2 This practice is for reflective insulation materials and radiant barrier materials intended for mechanical fastening to substrates or building structural members, or intended to be mounted to a substrate with an adhesive.1.3 Specimens of reflective insulation materials and radiant barrier materials intended for mechanical fastening shall be prepared and mounted in accordance with 6.1. Specimens of reflective insulation materials and radiant barrier materials intended to be mounted to a substrate with an adhesive shall be prepared and mounted in accordance with 6.2. If the reflective insulation material or sheet radiant barrier material includes manufacturer recommended installation instructions with the option to be installed either by mechanical attachment or adhered, the insulation material shall be tested by both mounting procedures as outlined in 6.1 and 6.2.1.4 Specimens of vinyl stretch ceiling materials shall be prepared and mounted in accordance with 6.1.NOTE 1: Vinyl stretch ceiling materials are mechanically fastened.1.5 This practice shall apply to reflective insulation materials and radiant barrier materials as defined in Section 3.1.6 This practice shall apply to reflective plastic core insulation materials as defined in 3.2.3. Reflective plastic core insulation materials are one specific type of reflective insulation materials.1.7 This practice shall apply to vinyl stretch ceiling materials as defined in Section 3.1.8 This practice shall not apply to rigid foam plastics with or without reflective facers.1.9 This practice shall not apply to site-fabricated stretch systems covered by Practice E2573.1.10 Testing is conducted in accordance with Test Method E84.1.11 This practice does not provide pass/fail criteria that can be used as a regulatory tool.1.12 Use the values stated in inch-pound units as the standard in referee decisions. The values in the SI system of units are given in parentheses, for information only; see IEEE/ASTM SI-10 for further details.1.13 This fire standard cannot be used to provide quantitative measures.1.14 Fire testing of products and materials is inherently hazardous and adequate safeguards for personnel and property shall be employed in conducting these tests. Fire testing involves hazardous materials, operations and equipment. This practice gives instructions on specimen preparation and mounting but the fire-test-response method is given in Test Method E84. See also Section 8.1.15 The text of this practice references notes and footnotes which provide explanatory material. These notes and footnotes (excluding those in tables and figures) shall not be considered requirements of the standard.1.16 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.1.17 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.

定价： 590元 / 折扣价： 502 元 加购物车

This specification establishes baseline performance requirements and additional optional capabilities for handheld point chemical vapor detectors (HPCVD) intended for homeland security applications. It provides HPCVD designers, manufacturers, integrators, procurement personnel, end users/practitioners, and responsible authorities a common set of parameters to match capabilities and user needs. The document specifies chemical detection performance requirements, system requirements, environmental requirements, manuals and documentation, product marking, and packaging.1.1 General: 1.1.1 This document presents baseline performance requirements and additional optional capabilities for handheld point chemical vapor detectors (HPCVD) for homeland security applications. This document is one of several that describe chemical vapor detectors (for example, handheld and stationary) and chemical detection capabilities including: chemical vapor hazard detection, identification, and quantification. An HPCVD is capable of detecting and alarming when exposed to chemical vapors that pose a risk as defined by the Acute Exposure Guideline Levels for Selected Airborne Chemicals (AEGL).1.1.2 This document provides the HPCVD baseline requirements, including performance, system, environmental, and documentation requirements. This document provides HPCVD designers, manufacturers, integrators, procurement personnel, end users/practitioners, and responsible authorities a common set of parameters to match capabilities and user needs.1.1.3 This document is not meant to provide for all uses. Manufacturers, purchasers, and end users will need to determine specific requirements including, but not limited to, use by HAZMAT teams, use in explosive atmospheres, use with personal protective equipment (PPE), use by firefighters and law enforcement officers, special electromagnetic compatibility needs, extended storage periods, and extended mission time. These specific requirements may or may not be generally applicable to all HPCVDs.1.2 Operational Concepts—HPCVDs are used to detect, identify, classify, or quantify, or combinations thereof, chemical vapor hazards that pose 30-min Acute Exposure Guideline Level-2 (AEGL-2) dangers. The HPCVD should not alarm to environmental background chemical vapors and should provide low false positive alarm rates and no false negatives. Uses of an HPCVD include search and rescue, survey, surveillance, sampling, and temporary fixed-site monitoring. An HPCVD should withstand the rigors associated with uses including, but not limited to, high- and low-temperature use and storage conditions; shock and vibration; radio frequency interference; and rapid changes in operating temperature, pressure, and humidity.1.3 HPCVD Chemical Detection Capabilities—Manufacturers document and verify, through testing, the chemical detection capabilities of the HPCVD. Test methods for assessing chemical detection capabilities are available from the Department of Homeland Security and the Department of Defense and are listed in Appendix X3.1.4 HPCVD System and Environmental Properties—Manufacturers document and verify, through testing, the system and environmental properties of the HPCVD. Example test methods for assessing the system and environmental properties are listed in Appendix X4.1.5 Units—The values stated in SI units are to be regarded as the standard. Vapor concentrations of the hazardous materials are presented in parts per million (ppm) as used in Acute Exposure Guideline Levels for Selected Airborne Chemicals, Vols 1-9 (see 2.1) and in mg/m3.1.6 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.

定价： 646元 / 折扣价： 550 元 加购物车

This specification deals with molybdenum wire and rod for electronic applications. The following grades of molybdenum wire and rod are covered in this specification: Grade 1—commercially pure molybdenum wire suitable for leads, hooks, supports, heaters, and metal-to-glass seals; Grade 2—commercially pure molybdenum wire suitable for mandrel either black or cleaned; and Grade 3—commercially pure molybdenum rod suitable for leads, hooks, supports, and metal-to-glass seals. Materials shall be tested and the individual grades shall conform to specified values of chemical composition, minimum tensile strength, elongation, ductility, surface finish, dimensional tolerances, and straightness.1.1 This specification covers two grades of molybdenum wire less than 0.050 in. (1.27 mm) in diameter and one grade of molybdenum rod 1.00 in. (25.4 mm) or less in diameter as follows:1.1.1 Grade 1—Commercially pure molybdenum wire suitable for leads, hooks, supports, heaters, and metal-to-glass seals.1.1.2 Grade 2—Commercially pure molybdenum wire suitable for mandrel either black or cleaned.1.1.3 Grade 3—Commercially pure molybdenum rod suitable for leads, hooks, supports, and metal-to-glass seals.1.2 The term wire applies to all spooled or coiled material and 0.050 in. (1.3 mm) or less in diameter and to short cut lengths 0.020 in. (0.51 mm) or less in diameter.1.3 The term rod applies to all material over 0.020 in. (0.51 mm) in diameter, supplied in straight lengths.1.4 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.1.5 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.

定价： 515元 / 折扣价： 438 元 加购物车

1.1 This practice describes the operation and production control of metal powder bed fusion (PBF) machines and processes to meet critical applications such as commercial aerospace components and medical implants. The requirements contained herein are applicable for production components and mechanical test specimens using powder bed fusion (PBF) with both laser and electron beams.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.

定价： 525元 / 折扣价： 447 元 加购物车

4.1 Walls, ceilings, and floors in building construction with improperly sealed joints, voids, or penetrations will not achieve the desired sound transmission loss. Proper sealing of joints, voids, and penetrations will increase sound transmission loss by reducing airborne sound flanking paths.1.1 This practice provides information for the use of sealants to reduce sound transmission characteristics of interior walls, ceilings, and floors by proper application of sealants to joints, voids, and penetrations normally found in building construction, which are commonly referred to as airborne sound flanking paths.1.2 The committee with jurisdiction over this standard is not aware of any comparable standards published by other organizations.1.3 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.1.4 This standard does not purport to address fire stopping or safing requirements for joints, voids, and penetrations through fire-rated wall, ceiling, and floor assemblies. Additional requirements may be necessary for fire-rated assemblies to meet the applicable building code provisions.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.

定价： 590元 / 折扣价： 502 元 加购物车

5.1 This test method provides procedures for obtaining tristimulus values, luminance factors and chromaticity coordinates of fluorescent-retroreflective materials by bispectral colorimetry using a 45:0 or 0:45 optical measuring system.5.2 The CIE 1931 (2°) standard observer is used to calculate the colorimetric properties of fluorescent-retroreflective sheeting and markings used in daytime high visibility traffic control and personal safety applications because in practice these materials are primarily viewed from a distance where they subtend less than 4° of the visual field.5.3 This test method is applicable to object-color specimens of any gloss level.5.4 Due to the retroreflective properties of these materials the colorimetric data may not be suitable for use in computer colorant formulation.5.5 This test method is suitable for quality control testing of fluorescent-retroreflective sheeting and marking materials.NOTE 1: Separation of the fluorescence and reflectance components from the total colorimetric properties provides useful and meaningful information to evaluate independently the luminescent and diffuse reflective efficiency and consistency of these materials.5.6 This test method is the referee method for determining the conformance of fluorescent-retroreflective sheeting and marking materials to standard daytime colorimetric specifications.1.1 This test method describes the instrumental measurement of the colorimetric properties (CIE tristimulus values, luminance factors, and chromaticity coordinates) of fluorescent-retroreflective sheeting and marking materials when illuminated by daylight.1.2 This test method is generally applicable to any sheeting or marking material having combined fluorescent and retroreflective properties used for daytime high visibility traffic control and personal safety applications.1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.5 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

定价： 590元 / 折扣价： 502 元 加购物车

1.1 This specification covers requirements for electrolytically formed oxide coatings on magnesium and magnesium alloy parts where appearance, abrasion resistance, and protection against corrosion are important.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.

定价： 515元 / 折扣价： 438 元 加购物车

5.1 This practice is a guideline for a screening test of candidate materials or assessment of local tissue response to absorbable medical devices which are expected to undergo complete absorption within three years.5.2 This practice is similar to those for studies on candidate materials or medical devices that are not absorbable, such as those specified in Practices F763, F981, and F1408; however, analysis of the host response must take into account the effect of degradation and degradation products on the inflammatory response at the local tissue site and on subsequent healing of the implantation site, as well as the potential for adverse distal tissue effects.5.3 For testing of absorbable medical devices, the test article for implantation should be in the final finished form as for intended use, including packaging and sterilization (if applicable). Configurations specific to the animal study may be needed. The test article’s surface-area-to-body mass or mass-to-body mass ratios within the animal model should be established by calculating based on surface-area-to-body mass or mass-to-body mass ratios in humans during the device’s intended clinical use. Worst-case clinical dose should be considered in the study design. For implantation studies incorporating evaluation of both local tissue responses and systemic toxicity, exaggerated material surface area or mass-to-body mass ratios (for example, a 2X to 10X safety factor to assess implant safety for regulatory submissions) compared to clinical use (for example, largest device size, maximum number of devices) should be considered, unless otherwise justified. For example, implantation of exaggerated doses may not be feasible in the selected animal model. For some devices, additional animal group(s) for exaggerated conditions should be considered if dose response information is needed. Additionally, for some devices, exaggerated dose at a specific implantation site can also be used to evaluate local tissue responses.5.4 Materials that are designed for use in devices with in situ polymerization shall be introduced in a manner such that in situ polymerization occurs. Additional testing of individual precursor components or partially polymerized materials may be needed in some cases (for example, if testing of the final implant indicates an adverse response or incomplete polymerization).1.1 This practice provides experimental protocols for biological assays of tissue reactions to absorbable biomaterials for implant applications. This practice applies only to absorbable materials with projected clinical applications in which the materials will reside in bone or soft tissue longer than 30 days and less than three years. Other standards with designated implantation times are available to address shorter time periods. Careful consideration should be given to the appropriateness of this practice for slowly degrading materials that will remain for longer than three years. It is anticipated that the tissue response to degrading biomaterials will be different from the response to nonabsorbable materials. In many cases, a chronic inflammatory response may be observed during the degradation phase, but the local histology should return to normal after absorption; therefore, the minimal tissue response usually equated with biocompatibility may require long implantations.1.2 The time period for implant absorption can depend on variables of chemical composition, implant size, implant location, and animal models. Therefore, the selected time points for assessing tissue effects may be selected based on the rate of absorption.1.3 These protocols assess the effects of the material on the animal tissue in which it is implanted. They do not fully assess systemic toxicity, carcinogenicity, reproductive and development toxicity, or mutagenicity of the material. Other standards are available to address these issues.1.4 To maximize use of the animals in the study protocol, some aspects of systemic toxicity, including effects of degradation products on different organs and tissues downstream of or surrounding the target site, can be addressed with this practice.1.5 Because animal models are not identical to human biology, this practice cannot account for all potential biological hazards, for example the effect of the oligosaccharide a-Gal (Gala 1,3-Galb1-4GlcNAc-R), known as the “a-Gal” epitope present in xenogeneic materials on humans. See ISO 22442.1.6 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.

定价： 590元 / 折扣价： 502 元 加购物车

X1.2 SignificanceX1.2.1 Concentrations of trace metals are measured as extracts in simulated body fluids. The metal’s concentration in extracts is based on the surface area of the plastic extracted from which the total amount of metal deliverable to the patient may be estimated.AbstractThis specification covers the properties for polyethylene plastics for use in medical device applications involving human tissue contact devices, short term indwellings, and fluid transfer devices. Biocompatibility tests must be conducted on the final products as the biocompatibility of these materials as a class has not been established. Plyethylene plastics should consist of basic polymers with ethylene as essentially the sole monomer. The compound may contain optional adjuvant substances required in polymer production or fabrication. The final compound should yield a consistent absorption spectrum characteristic of the established formulation. The polyethylene plastics should be tested using the specified physical test procedures for density, melt flow, tensile properties, compressive properties, stiffness, flexural fatigue, and other flexural properties.1.1 This specification covers polyethylene plastics (as defined in Terminology D883) intended for use in medical device applications involving human tissue contact devices, short-term indwellings of 30 days or less, and fluid transfer devices. The biocompatibility of these materials as a class has not been established. Biocompatibility tests must be conducted on the final product.1.2 This specification is not applicable to ultra-high molecular weight polyethylenes (UHMWPE) plastics, such as those used in joint implants, and so forth.1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

定价： 515元 / 折扣价： 438 元 加购物车

This specification covers steel tubes, carbon and carbon manganese, fusion welded, for boiler, superheater, heat exchanger and condenser application. After welding, all tubes shall be heat treated and followed by cooling in air or in the cooling chamber of a controlled atmosphere furnace. The steel shall conform to the required chemical compositions. The tensile and hardness test requirements to all tube prior to cutting are presented. Mechanical testing requirements indicates that, one flattening test shall be made on specimens from each of two tubes from each lot or fraction thereof, one flange test shall be made on specimens from each of two tubes from each lot or fraction thereof, one crush test shall be made on specimens from each of two tubes from each lot or fraction thereof, and one reverse flattening test shall be made on each 1500 ft [450 m] of finished tubing. Finally, each tube shall be subjected to either the hydrostatic or the non-destructive electric test.1.1 This specification covers minimum wall thickness welded tubes made from carbon and carbon manganese steels listed in Table 1, with various grades intended for use in boiler, superheater, heat exchanger, or condenser applications.TABLE 1 Chemical Requirements, Composition, %Element Grade ALow CarbonSteel Grade CMedium CarbonSteel Grade DCarbon ManganeseSteelCarbon 0.06–0.18 0.30 max 0.27 maxManganese 0.27–0.63 0.80 max 1.00–1.50Phosphorus 0.035 max 0.035 max 0.030 maxSulfur 0.035 max 0.035 max 0.015 maxSilicon No Requirement No Requirement 0.10 min1.2 The tubing sizes and thicknesses usually furnished to this specification are 1/4 to 5 in. [6.3 to 127 mm] in outside diameter and 0.015 to 0.375 in. [0.4 to 9.5 mm], inclusive, in wall thickness. Tubing having other dimensions may be furnished provided such tubes comply with all other requirements of this specification.1.3 Mechanical property requirements do not apply to tubing smaller than 1/8 in. [3.2 mm] in inside diameter or 0.015 in. [0.4 mm] in thickness.1.4 The values stated in either inch-pound units or SI units are to be regarded separately as standard. Within the text, the SI units are shown in brackets. The values stated in each system are not exact equivalents; therefore, each system must be used independently of the other. Combining values from the two systems may result in nonconformance with the specification. The inch-pound units shall apply unless the “M” designation of the specification is specified in the order.1.5 Optional supplementary requirements are provided and when desired, shall be so stated on the purchase order.1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory requirements prior to use.

定价： 0元 / 折扣价： 0 元

This specification covers the requirements and test methods for outside diameter controlled, pressure rated, black metric-sized and IPS-sized crosslinked polyethylene (PEX) pipe, fittings and joints intended for oil and gas producing applications. It presents the criteria for materials made in pipe dimension ratios ranging from 6 to 17, along with workmanship, burst pressure, hydrostatic sustained pressure, bent-pipe hydrostatic pressure, stabilizer functionality, degree of crosslinking, and chemical resistance. It also includes guidelines for pipe and fittings markings.1.1 This specification covers outside diameter controlled, pressure rated, metric-sized and inch-sized black or yellow crosslinked polyethylene (PEX) pipe made in pipe dimension ratios ranging from 6 to 17. Included are requirements and test methods for material, workmanship, dimensions, burst pressure, hydrostatic sustained pressure, stabilizer functionality, bent-pipe hydrostatic pressure, degree of crosslinking, chemical resistance, and minimum operating temperature. Requirements for pipe markings are also given. The pipe covered by this specification is intended for pressure or non-pressure oil and gas producing applications, such as conveying oil, dry or wet gas, gas gathering, multiphase fluids, and non-potable oilfield water. This specification does not cover piping for gas distribution applications.1.2 This specification also includes requirements for joints made between PEX pipe and polyethylene electrofusion fittings (specified in Specifications F1055 or F3373). Fittings to be used with PEX pipe manufactured to this Specification are in Specification F2829/F2829M. Installation considerations are in Appendix X3.1.3 The text of this specification references notes, footnotes, and appendixes, which provide explanatory material. These notes and footnotes (excluding those in tables and figures) shall not be considered as requirements of the specification.1.4 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 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.NOTE 1: Metric sized (SI units) pipe should only be joined with corresponding metric sized fittings, and inch sized pipe should only be joined with corresponding inch sized fittings. Inch sized fittings should not be used for metric sized pipe, and metric sized fittings should not be used for IPS inch sized pipe.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.

定价： 590元 / 折扣价： 502 元 加购物车

5.1 The purpose of this guide is to provide guidance on characterization of the properties of porcine fibrinogen as a starting material for surgical implants and as a matrix for tissue-engineered medical products (TEMPs). This guide contains a set of physical and chemical parameters directly related to the function of porcine fibrinogen. This guide can be used to help select and characterize appropriate fibrinogen starting materials for specific purposes. Not all tests or parameters are suitable for all uses of fibrinogen.5.2 Fibrinogen described in this guide may be used in various types of medical products including, but not limited to, implants, tissue-engineered medical products (TEMPs), and cell, drug, or DNA delivery vectors. The recommendations in this guide shall not be construed to guarantee the successful clinical application of any tissue-engineered medical product.5.3 In determining whether fibrinogen meets the requirements for use in a TEMP, the relevant regulatory authorities or other appropriate guidelines relating to the production, regulation, and approval of TEMP products shall be taken into account (Guide E1298, Practice F981, Practice F1983).1.1 This guide covers the evaluation of porcine fibrinogen suitable for use in biomedical or pharmaceutical applications including, but not limited to, tissue-engineered medical products (TEMPs).1.2 This guide addresses key parameters relevant for functionality, characterization, and purity of porcine fibrinogen.1.3 As with any material, some characteristics of porcine fibrinogen may be altered by processing techniques, such as electrospinning (1)2 and sterilization, required for the production of a specific formulation or device. Therefore, properties of fabricated forms of this protein should be evaluated using test methods that are appropriate to ensure safety and efficacy and are not addressed in this guide.1.4 The primary focus of this document is fibrinogen derived from porcine blood, which is similar to human fibrinogen. The biggest advantage that pigs have over other species (such as cattle, sheep, goats, elk, and deer) is that they are less likely to transmit transmissible spongiform encephalitis (TSE) (ISO 22442-1 Annex D; WHO Guidelines, 2003; WHO Guidelines, 2006; WHO Guidelines, 2010). The document may also discuss fibrinogen from other sources when useful information is available. Fibrin is also discussed in some sections.1.5 Units—The values stated in SI units are to be regarded as the standard. No other units of measurement are included in this standard.1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

定价： 590元 / 折扣价： 502 元 加购物车

This specification covers composite ribbed steel pipe, precoated and polyethyene lined intended for use for gravity flow sanitary sewers, storm sewers, and other special applications such as water transmission pipe, rehabilitation pipe, slip line pipe, and irrigation pipe. Pipes shall be fabricated in full circular cross-section with helical lock seams and helical ribs projecting outwardly. Specimens cut from production pipe normal to and across the lock seam shall conform to the required values of tensile strength. The pipe shall conform to the required values of nominal inside diameter and sheet thickness. Joint connectors for composite ribbed steel pipe precoated and polyethylene lined shall be specified as soil tight, water-resistant, or watertight.1.1 This specification covers composite ribbed steel pipe, precoated and polyethylene lined intended for use for gravity flow sanitary sewers, storm sewers, and other special applications such as water transmission pipe, rehabilitation pipe, slip line pipe, and irrigation pipe where extra corrosion and abrasion resistance are required. The steel sheet used in the fabrication of the pipe has a polymer coating over a metallic coating of zinc on both sides. In addition, as the pipe is being fabricated, the ribs are filled with polyethylene and then a polyethylene liner is extruded onto the interior surface.1.2 The exterior polymer precoating provides extra protection of the steel against soilside corrosion, in addition to that provided by the metallic coating, and also provides a dielectric barrier for cathodic protection. The interior polymer precoating provides an adhesive layer between the galvanized steel and the polyethylene lining. The applied lining provides internal protection against corrosion, erosion, and abrasion. By filling the rib which has a deltoid shape (smaller at the opening in the pipe wall than at the bottom of the rib), the polyethylene is mechanically connected to the pipe wall and the polyethylene liner is then thermally bonded to the filled rib.1.3 This specification does not include requirements for bedding, backfill, or the relationship between earth cover load and sheet thickness of the pipe. Experience has shown that the successful performance of this product depends upon the proper selection of sheet thickness, type of bedding and backfill, controlled manufacture in the plant, and care in the installation. The installation procedure is described in Practice A798/A798M.1.4 This specification is applicable to orders in either inch-pound units as A978, or in SI units as A978M. Inch-pound units and SI units are not necessarily equivalent. SI units are shown in brackets in the text for clarity, but they are the applicable values when the material is ordered to A978M.1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

定价： 0元 / 折扣价： 0 元

1.1 This specification establishes the requirements for hard-drawn, seamless capillary tube made from Copper Alloy UNS Nos. C10800, C12000, or C12200.1.2 This tube is commonly supplied in straight lengths intended for restrictor applications such as metering lines for liquids and gases where close control over smoothness and diameter of the bore is required to insure uniform flow characteristics between tubes.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.

定价： 590元 / 折扣价： 502 元 加购物车

4.1 When more than one elastomer seal material is tested, the test methods yield comparative data on which to base judgements as to expected service quality. Suggested in-service property change limits are provided. Property changes beyond these limits will indicate limited service life of the elastomer seal.4.2 These test methods attempt to simulate service conditions through controlled aging and evaluation of property changes but may not give any direct correlations with actual part performance since actual service conditions vary widely. These test methods yield comparative data and indications of property changes of the elastomeric seal material under ideal service conditions. These test methods can be used for quality control purposes, for engineering assessments, for service evaluation, and for manufacturing control. The information from these test methods can be used to anticipate expected service quality.1.1 These test methods cover the procedure for measuring physical properties of elastomer seals in the form of O-rings after exposure to industrial hydraulic fluids and thermal aging. The measured properties are then compared to the physical properties of elastomer seals that have not been exposed to the industrial hydraulic fluids and thermal aging. The changes in these properties form a basis for assessing compatibility when these changes are compared against the suggested limits in Table 1.1.2 While these test methods involve the use of O-rings, they can also be used to evaluate the compatibility of the elastomeric compounds of specialty seals with industrial hydraulic fluids and their resistance to thermal aging. The compounds can be molded into O-rings for evaluation purposes.1.3 These test methods provide procedures for exposing O-ring test specimens to industrial hydraulic fluids under definite conditions of temperature and time. The resulting deterioration of the O-ring material is determined by comparing the changes in work function, hardness, physical properties, compression set, and seal volume after immersion in the test fluid to the pre-immersion values.1.4 The values stated in SI units are to be regarded as the standard.1.4.1 Exception—The values given in parentheses are for information only.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.

定价： 590元 / 折扣价： 502 元 加购物车