Combined Cycle Water Chemistry_POWER

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Combined-Cycle Water/Steam Monitoring11/14/2013

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By Brad Buecker, Contributing EditorEarlier in this series, I wrote about modern techniques to minimize impurity ingress, scaling, and corrosion in heat recovery steam generators (HRSG). But without accurate sampling and good data collection, the conditions within an HRSG may be or become harmful without the knowledge of operators or other technical personnel.This is another of those cases where an "ounce of prevention is worth a pound of cure." This article outlines important samples required for successful HRSG operation.Monitoring the Entire SystemOrganizations such as the Electric Power Research Institute (EPRI) have written entire manuals regarding HRSG sampling [2], so obviously a complete overview is not possible in a single technical article. However, it is possible to discuss the most important samples and the benefits derived thereby.HRSGs come in many different designs, but a common general arrangement is shown in Figure 1. We will use it for this discussion.

Let's begin at the condenser and condensate pump discharge (CPD), with the note that many HRSGs are not equipped with condensate polishers. For units with water-cooled condensers, the condenser is the primary source within the system for impurity ingress. Even a minor leak from one condenser tube can introduce enough impurities to cause significant damage in the evaporator circuits. In the opinion of many, the CPD sample point is the most important of any within the entire water/steam network.Where the condensate is treated by a polisher, the effects of a condenser tube leak are dampened. However, it is still important that any leak be detected as quickly as possible to prevent premature exhaustion of the polisher and subsequent carryover of contaminants to the boiler.Recommended on-line analyses include: Cation Conductivity (or becoming popular, degassed cation conductivity) Sodium Dissolved OxygenThe name for cation conductivity has undergone an evolution, and research groups have now begun referring to the technique as conductivity after cation exchange (CACE). For this article, we will continue to use cation conductivity. The technique has been adopted at most plants for detecting impurity in-leakage. If a condenser tube fails or impurities enter from another source (a makeup water treatment system failure is the next most likely source), the sodium, calcium, and magnesium salts in the water are converted to their respective acids, primarily dilute sulfuric and hydrochloric acids, by the cation exchange column.

The dilute acids that emerge (HCl and H2SO4, primarily) are more conductive than their respective salts and have an immediate influence on conductivity, thus providing a quick indication of upsets. The cation column also removes ammonium ions (NH4+), which are formed by conditioning chemicals added to the feedwater. If ammonium ions are not removed from the sample, they can mask impurities. In general, the cation conductivity of a clean condensate sample should be less than 0.2 micromhos (microsiemens) per centimeter (S). This limit is mandatory for systems that operate on all-volatile treatment oxidizing [AVT(O)], which has been developed to minimize flow-accelerated corrosion in economizers and evaporator tubes. [3]So, how does degassed cation conductivity improve upon the method? Air that leaks into condensers of course contains a small percentage of carbon dioxide. At significant air in-leakage rates, the CO2 that enters can increase the condensate conductivity and mask other impurity ingress. Degassed cation conductivity utilizes either a reboiler or purge vessel (with nitrogen gas feed) to remove carbon dioxide.Direct sodium monitoring of the CPD is also very effective for detecting condenser leaks and other impurity ingress. With a tight condenser, sodium levels in the condensate should be very low (