ASTM-D5357 Historical Revision Information
Standard Test Method for Determination of Relative Crystallinity of Zeolite Sodium A by X-ray Diffraction

ASTM-D5357 - 2003 R08(E1) EDITION - SUPERSEDED
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Standard Test Method for Determination of Relative Crystallinity of Zeolite Sodium A by X-ray Diffraction
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Scope

1.1 This test method covers a procedure for determining the relative crystallinity of zeolite sodium A (zeolite NaA) using selected peaks from the X-ray diffraction pattern of the zeolite.

1.2 The term intensity of an X-ray powder diffraction (XRD) peak refers to the integral intensity, either the area or counts under the peak or the product of the peak height and the peak width at half height.

1.3 This test method provides a number that is the ratio of intensity of portions of the XRD pattern of the sample to intensity of the corresponding portion of the pattern of a reference zeolite NaA. The intensity ratio, expressed as a percentage, is then labeled relative crystallinity of NaA.

1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this 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 and health practices and determine the applicability of regulatory limitations prior to use.

Significance and Use

Zeolite NaA has been used as an active component in molecular sieves employed as desiccants for natural gas, process gas streams, sealed insulated windows, and as a builder (water softener) in household laundry detergents.

This X-ray procedure is designed to allow a reporting of the relative degree of crystallization of NaA in the manufacture of NaA. The relative crystallinity number has proven useful in technology, research, and specifications.

Drastic changes in intensity of individual peaks in the XRD pattern of NaA can result from changes in distribution of electron density within the unit cell of the NaA zeolite. The electron density distribution is dependent upon the extent of filling of pores in the zeolite with guest molecules, and on the nature of the guest molecules. In this XRD method, the guest molecule H2O completely fills the pores. Intensity changes may also result if some or all of the sodium cations in NaA are exchanged by other cations.

Drastic changes in overall intensity can result from changes in X-ray absorption attributed to non-crystalline phases, if present, in a NaA sample. If non-zeolite crystalline phases are present, their diffraction peaks may overlap with some of the NaA diffraction peaks selected for this test method. If there is reason to suspect the presence of such components, then NaA peaks free of interference should be chosen for analysis.

Keywords

crystallinity; X-ray diffraction; zeolite sodium A; Crystallinity; Relative crystallinity; X-ray diffraction analysis; Zeolite catalysts; ICS Number Code 71.040.30 (Chemical reagents)

To find similar documents by ASTM Volume:

05.05 (Combustion Characteristics; Manufactured Carbon and Graphite Products; Catalysts)

05.06 (Gaseous Fuels; Coal and Coke)

To find similar documents by classification:

71.040.30 (Chemical reagents Including reference materials)

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Document Number

ASTM-D5357-03(2008)e1

Revision Level

2003 R08(E1) EDITION

Status

Superseded

Modification Type

Reapproval

Publication Date

May 1, 2008

Document Type

Test Method

Page Count

3 pages

Committee Number

D32.05