ASTM D3069-1994(2013) Standard Test Method for Delivery Rate of Aerosol Products《气溶胶制品输送率的标准试验方法》.pdf
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1、Designation: D3069 94 (Reapproved 2013)Standard Test Method forDelivery Rate of Aerosol Products1This standard is issued under the fixed designation D3069; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last revision.
2、A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.This standard has been approved for use by agencies of the Department of Defense.1. Scope1.1 This test method covers the determination of deliver
3、yrate of aerosol products.1.2 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the user of this standard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations pr
4、ior to use.2. Referenced Documents2.1 ASTM Standards:2D996 Terminology of Packaging and Distribution Environ-ments3. Terminology3.1 General definitions for packaging and distribution envi-ronments are found in Terminology D996.4. Summary of Test Method4.1 The delivery rate of an aerosol dispenser is
5、 determinedby measuring the quantity of material expelled through thevalve in a given time. The exact duration of discharge and thetemperature of the dispenser must be carefully controlled forgood reproducibility.4.2 Biological and clinical tests are often made with one ortwo dispensers selected fro
6、m a group that is similar in allrespects, with the exception of delivery rate. When it isdesirable to select dispensers with equal delivery rates, threetests should be performed on each dispenser.4.3 In the case of storage tests, a single delivery rate test isnormally performed at each examination p
7、eriod to conserve thecontents and extend the life of the dispenser.5. Significance and Use5.1 Delivery rate tests assist in evaluating one aspect ofvalve performance, and are considered as a prerequisite to bothbiological and storage testing.6. Apparatus6.1 Water Bath, maintained at 70 6 0.5F (21 6
8、0.25C)(80 6 0.5F (26 6 0.25C) for insecticides), to matchPeet-Grady test requirements, with a screen or perforated metalshelf 1 in. (25 mm) above the bottom of the bath.6.2 Stirrer, air or electric.6.3 Balance, 0.1-g scale.6.4 Stop Watch or Electric Timer .7. Sampling7.1 Normal production or laborat
9、ory samples shall be usedfor this test.8. Test Specimen8.1 Remove the protective cover, paper label, and all otherdetachable materials from the dispenser, with the exception ofthe button or actuator.8.2 If a foam spout is used, remove the spout, cut away allnonessential plastic, and then replace the
10、 spout.9. Procedure9.1 Activate the valve for a few seconds, then remove anyvalve cup impingements, and weigh the dispenser to thenearest 0.05 g.9.2 Place the dispenser on the shelf in the water bath, whichis maintained at the test temperature of 70 6 0.1F (21 60.05C). Keep the dispenser in an uprig
11、ht position, spaced 1 in.(25 mm) apart, and covered with 1 in. of water.NOTE 1Approximately 0.03 % sodium nitrite (NaNO2) may be addedto the water bath to prevent the minor rusting of some tinplate dispensers.9.3 Circulate the water with the mechanical stirrer. Hold for15 min in the case of essentia
12、lly anhydrous products, and for25 to 30 min for viscous or water-base products.NOTE 2In the case of thixotropic, rheopectic, and certain other1This test method is under the jurisdiction of ASTM Committee D10 onPackaging and is the direct responsibility of Subcommittee D10.33 on MechanicalDispensers.
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