1.1 These practices cover detecting leaks in which there is a direct communication between the feed or concentrate, or both, and the permeate. Several types of leaks are possible with the various configurations of reverse-osmosis devices.
1.2 Types of Leaks:
1.2.1 With hollow-fiber devices, feed or concentrate leakage, or both, into the permeate stream by leaks through the tube sheet and past the tube sheet O-ring are possible. “Leaks” caused by broken fibers are not covered by these practices.
1.2.2 With spiral-wound devices, leaks may occur through damage of the membrane surface itself by punctures or scratches, by glue-line failure, and by O-ring leaks on product tube interconnectors.
1.2.3 With tubular devices, leaks due to membrane damage, tube end seal leaks, and leaks from broken tubes or product headers are possible.
1.3 Three leak test practices are given as follows:
Sections Practice A – Tube Sheet and O-Ring Leak Test for Hollow Fiber 6 to 9 Devices Practice B – Vacuum Test for Spiral Wound Devices 10 to 12 Practice C – Dye Test for Spiral Wound and Tubular Devices 13 to 18
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.
Product Details
- Published:
- 12/10/1998
- Number of Pages:
- 3
- File Size:
- 1 file , 33 KB
