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Standard Test Methods for Internal Pressurization Failure Resistance of Unrestrained Packages
Automaticky přeložený název:
Standardní zkušební metody pro vnitřní natlakování Porucha Odpor bezuzdné balíčků
NORMA vydána dne 1.8.2007
Označení normy: ASTM F1140-07
Poznámka: NEPLATNÁ
Datum vydání normy: 1.8.2007
Kód zboží: NS-49265
Počet stran: 5
Přibližná hmotnost: 15 g (0.03 liber)
Země: Americká technická norma
Kategorie: Technické normy ASTM
Keywords:
burst, closed package, creep, flexible packaging, inflation, medical packaging, open package, ICS Number Code 55.180.40 (Complete, filled transport packages)
Significance and Use | ||||||
These test methods provide a rapid means of evaluating tendencies for package failure when the package is exposed to a pressure differential. Pressure differentials may occur during processes such as sterilization and transportation. These test methods are frequently used to quickly evaluate packages during the manufacturing process and at various stages of the package’life cycle. If correlations between pieces of test equipment are to be made, it is important that all parameters of the test method be exactly the same. Typical parameters may include, but are not limited to, package size, material, seal configuration, test equipment, rate of air flow into the package, sensitivity (machine response to pressure drop), and position of test article (see Fig. 1). These test methods do not necessarily provide correlation with actual package seal strength as typically measured using Test Method F 88 (or equivalent).
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1. Scope | ||||||
1.1 These test methods explain the procedure for determining the ability of packages to withstand internal pressurization. 1.2 The burst test increasingly pressurizes the package until the package fails. 1.3 The creep test maintains a specified pressure for a specified time or until the package fails. 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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