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ASTM E1157-87(1996)
Standard Specification for Sampling and Testing of Reusable Laboratory Glassware
Automaticky přeložený název:
Standardní Specifikace pro odběr vzorků a testování opakovaně použitelných laboratorního skla
NORMA vydána dne 10.10.1996
Informace o normě:
Označení normy: ASTM E1157-87(1996)
Poznámka: NEPLATNÁ
Datum vydání normy: 10.10.1996
Kód zboží: NS-40657
Počet stran: 4
Přibližná hmotnost: 12 g (0.03 liber)
Země: Americká technická norma
Kategorie: Technické normy ASTM
Anotace textu normy ASTM E1157-87(1996) :
Keywords:
Acid test, Alkali test, Autoclaves, Beakers, Blown and pressed glassware, Bottom-zone bottles, Capacity, Centrifuge method, Classification, Classification of defects, Defects, Funnels, Graduated laboratory apparatus, Inspection, Jars, Kettles, Knots, Laboratory apparatus, Leak testing, Nongraduated glassware, Reusable laboratory apparatus, Sampling, Tubular glassware (graduated/non-graduated), sampling/inspection/testing reusable laboratory glassware, spec
Doplňující informace
| 1. Scope | ||||||||
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1.1 This specification covers laboratory items for use until they are no longer considered functional for the intended purpose. It is written specifically for reusable items and is not to be confused with disposable (single use) items that are described in other standards. 1.2 This specification covers the sampling inspection and basic testing criteria for the following four types of laboratory glassware: blown and pressed glassware, nongraduated ; blown and pressed glassware, graduated ; tubular glassware, nongraduated; and tubular glassware, graduated. 1.3 This specification is intended to be used in conjunction with a standard specification for a specific laboratory glassware product. 1.4 The following precautionary statement pertains only to the test method portion, Section 6, of this specification. This standard does not purport to address all of the safety problems, 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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