Formerly under the jurisdiction of Committee D19 on Water, this practice was withdrawn in January 2019 in accordance with section 10.6.3 of the Regulations Governing ASTM Technical Committees, which requires that standards shall be updated by the end of the eighth year since the last approval date.
Значение и использованиеDuring the operation of an RO system, system conditions such as pressure, temperature, conversion, and feed concentration can vary, causing permeate flow and salt passage to change. To effectively evaluate system performance, it is necessary to compare permeate flow and salt passage data at the same conditions. Since data may not always be obtained at the same conditions, it is necessary to convert the RO data obtained at actual conditions to a set of selected constant conditions, thereby standardizing the data. This practice gives the procedure to standardize RO data.
This practice can be used for both spiral wound and hollow fiber systems.
This practice can be used for a single element or a multi-element system. However, if the RO system is brine staged, that is, the brine from one group of RO devices is the feed to a second group of RO devices, standardize the permeate flow and salt passage for each stage separately.
This practice is applicable for reverse osmosis systems with high rejections and with no significant leaks between the feed-brine and permeate streams.
Область применения1.1 This practice covers the standardization of permeate flow and salt passage data for reverse osmosis (RO) systems.
1.2 This practice is applicable to waters including brackish waters and seawaters but is not necessarily applicable to waste waters.
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.4 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.