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Standard Specification for Liquid Crystal Polymers (Includes all amendments And changes 8/16/2017).
Automaticky preložený názov:
Štandardné špecifikácie pre Liquid Crystal polymérov
NORMA vydaná dňa 10.11.1999
Označenie normy: ASTM D5138-99a
Poznámka: NEPLATNÁ
Dátum vydania normy: 10.11.1999
Kód tovaru: NS-29987
Počet strán: 7
Približná hmotnosť: 21 g (0.05 libier)
Krajina: Americká technická norma
Kategória: Technické normy ASTM
Keywords:
Aromatic polyester (ARP), extrusion materials, injection molding materials, line call out specification, liquid crystal polymers (LCP), recycled plast, ICS Number Code 31.120 (Electronic display devices)
| 1. Scope | ||||||||||||||||||||||||||||||||
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1.1 This specification covers liquid crystal polymeric materials suitable for injection molding and extrusion. 1.2 The properties included in this specification are those required to identify the compositions covered. There may be other requirements necessary to identify particular characteristics important to specialized applications. These shall be agreed upon between the user and the supplier, by using the suffixes as given in Section 5. 1.3 This specification is intended to be a means of calling out plastic materials used in the fabrication of end items or parts. It is not intended for the selection of materials. Material selection should be made by those having expertise in the plastic field after careful consideration of the design and the performance required of the part, the environment to which it will be exposed, the fabrication process to be employed, the inherent properties of the material other than those covered by this specification, and the economics. 1.4 The values stated in SI units are to be regarded as the standard. 1.5 The following precautionary caveat pertains only to the test method portion, Section 11, of this specification: 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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| 2. Referenced Documents | ||||||||||||||||||||||||||||||||
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