ASTM D6807-02(2009) PDF

1.1 This test method covers the determination of the operating characteristics of continuous electrodeionization (CEDI) devices, indicative of deionization performance when a device is applied to production of highly deionized water from the product water of a reverse osmosis system. This test method is a procedure applicable to feed waters containing carbonic acid and/or dissolved silica and other solutes, with a conductivity range of approximately 2 to 100 microsiemens-cm^-1.

1.2 This test method covers the determination of operating characteristics under standard test conditions of CEDI devices where the electrically active transfer media therein is predominantly regenerated.

1.3 The test method is not necessarily indicative of:

1.3.1 Long term performance on feed waters containing foulants and/or sparingly soluble solutes;

1.3.2 Performance on feeds of brackish water, sea water, or other high salinity feeds;

1.3.3 Performance on synthetic industrial feed solutions, pharmaceuticals, or process solutions of foods and beverages; or,

1.3.4 Performance on feed waters less than 2 μS/cm, particularly performance relating to organic solutes, colloidal or particulate matter, or biological or microbial matter.

1.4 The test method, subject to the limitations described, can be applied as either an aid to predict expected deionization performance for a given feed water quality, or as a method to determine whether performance of a given device has changed over some period of time. It is ultimately, however, the user's responsibility to ensure the validity of the test method for their specific applications.

1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.

1.6 This standard may involve hazardous materials, operations, and equipment. 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.