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Control is by simple  boiler water tests or RX CLEANSERS  can provide a suitable test  kits for this purpose.

Used in low pressure and auxillary boilers

:::::::::::::::::::::Alkalinity  TEST FOR BOILER & COOLING WATER ::::::::::::::::::::::::

REAGENT & APPARATUS :
Reagent:  RXSOL TK 7 , TK 8 , TK 9 , . Apparatus : TEST TUBE , Titrator or DROPPER

PROCEDURE for p-ALKALINITY  test ( STEP WISE ):

1. Measure 10 ml of SAMPLE WATER in graduated TEST TUBE / CYLINDER
2. Add 1-2 drops of  RXSOL TK7 and mix with the stirring rod , If  sample turns red / PINK ( which indicates presence of p-Alkalinity ) then follows 3^rd step otherwise if sample remains colourless ( Record p-Alkalinity = 0 ) .
3. Add RXSOL TK9  drop by drop ( by counting ) , mixing with the stirring rod until colour just disappears. Each drop is equivalent to 25 ppm of p-Alkalinity , expressed as CaCO₃

RESULT  : Each DROPS is equivalent to  25 PPM of Alkalinity .

NOTE :    p-Alkalinity VALUE  =  25 X ( Total Number of DROPS of TK9 , during 3^rdstep  )

PROCEDURE for p-ALKALINITY  & TOTAL ALKALINITY ( STEP WISE ):

1. Measure 10 ml of SAMPLE WATER in graduated TEST TUBE / CYLINDER
2. Add 1-2 drops of  RXSOL TK7 and mix with the stirring rod , If  sample turns red / PINK ( which indicates presence of p-Alkalinity ) then follows 3^rd step otherwise if sample remains colourless ( Record p-Alkalinity = 0 ) then proceed to STEP- 4.
3. Add RXSOL TK9  drop by drop ( by counting ) , mixing with the stirring rod until colour just disappears. Each drop is equivalent to 15 ppm of p-Alkalinity , expressed as CaCO₃
4. Add 2-3 drops of RXSOL TK8 and mix with stirring rod , the sample will turn to BLUISH-GREEN .
5. AddRXSOL TK9 carefully by counting drop by drop and mixing throughly until a light reddish  pink  colour develop.

RESULT  : Each DROPS is equivalent to 25 PPM of Alkalinity .

NOTE :    p-Alkalinity ppm CaCO₃VALUE ( A )  =  25 X ( Total Number of DROPS of TK9 , during 3^rdstep  )

Total Alkalinity ppm CaCO₃VALUE  =  A +  { 25 X ( Total Number of DROPS of TK9 , during 5^th step  )}

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OTHER VALUABLE PRODUCTS 

Basic Boiler System Schematic

Below is a summary of problems associated with the common impurities in water and solutions to each problem.

List Of Problems Caused By Impurities In Water

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Chemical feed should be continuous. Chemical pumping rates can create problems especially for neat feed set ups. Using on/off feed systems such as a recycle timer can create problems. Chemical feed pumps should be sized or product strengths should be adjusted to allow continuous feed.

Steam and carbon dioxide leave continuously, so setting up a neutralizing amine pump to feed intermittently can lead to wide variations in condensate pH control. If sampling is done from a condensate receiver, the tank volume may buffer the variations and the changes may not be noticed, but corrosion could be occurring to areas of the piping that see the rapidly changing pH.


If polymeric dispersants, phosphonates, phosphate, or chelants are fed intermittently into the feedwater using a recycle timer, and the amines are not fed continuously, a cycle of iron slugs returning in the condensate can be followed by slugs of high dispersancy cleaning of the iron from the deaerator and dragging it into the boiler.

Load changes can affect chemical concentrations when the chemical feed is base fed. Example: Steam production of one million lbs./day; 4% blowdown; 20% active boiler polymer product fed at 5 pounds per day. The calculated daily average polymer concentration would be 24 ppm. Assume peak plant production load is 60,000 lbs./hr., but during the overnight hours the load is only 5,000 lbs./hr. If the dispersant is being fed continuously over the 24 hours, during the 8- hour low load period, the boiler polymer concentration would have increased to over 200 ppm. Upon high fire when production resumes, carryover is very possible because of over concentrating the polymeric dispersant.

Chemical feed needs to be paced to steam production, especially where significant load changes occur.

Carbon dioxide can concentrate in steam and condensate making neutralizing amine treatment impractical. Carbon dioxide levels can be relatively low in steam exiting a boiler at only a few ppm, but if there are areas where it becomes “trapped” and can accumulate, concentrations can reach extremely high levels into the hundreds or even thousands of ppm.

CO2 is a non-condensable gas. It has a distribution ratio in the steam piping and condenses at points throughout the system. At the boiling point, the solubility of the gas in water is extremely low. The solubility of the CO2 is actually lower in the condensate than it is in the steam. For the CO2 to escape from the steam into the water it will accumulate in the steam space just above the water level until the partial pressure becomes high enough for the CO2 in the incoming steam to be able to exit into the condensate. This creates a steady state condition of CO2 coming in and exiting, but an area of severe localized corrosion occurs where the carbon dioxide concentration is high.

The highest CO2 concentration normally occurs just above the condensate water level. If there is an area where condensation is occurring and running down pipes or the sides of vessels, the CO2 concentration will be very high and the pH will be about 5.3 – 5.5 in that location creating high corrosion rates.


The solubility of CO2 increases dramatically as the condensate temperature falls below 212 °F. When there is an accumulation of CO2 in an area and the condensate temperature is relatively low, the amount of carbon dioxide going into solution will be extremely high. Where low-pressure steam is used that contains CO2 and the heat exchange process has relatively close temperature differentials between the steam and the condensate, there is potential for high uptake of the CO2 into the condensate and localized low pH.

Neutralizing amines are selected in an effort to condense in the right concentrations to carbon dioxide condensation levels throughout the steam system. Neutralizing amines cannot control corrosion where this localized accumulation of carbon dioxide occurs since the high CO2 overwhelms the demand for the amine. Even point source addition of amine may not be able to satisfy the demand.

Where the concentrating effect of CO2 occurs, methods of reducing the problem include eliminating or minimizing CO2 in the steam, venting off the CO2 in the localized area, eliminating condensate in the area, applying a filming amine or metal passivator, or using higher temperature steam and increasing condensate temperature to reduce the CO2 content in the condensate.

 Company Details:

RX MARINE INTERNATIONAL
105, A wing , BSEL , TECH PARK.
VASHI ,NEW BOMBAY 400703 INDIA

*See Section 16

Corrosive

-  Non combustible
-  Not flammable. In case of fire use extinguishing media appropriate to surrounding conditions

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-  This article is considered stable under normal conditions
-  Avoid over heating, Keep away from frost
-  In compatible with acid
-  See Section 5

Text of Rand Sphrase codes used in this safety data sheet:-R22: Harmful if swallowed;R35: Causes severe burns.The information provided about the product on this Safety Data Sheet has been compiled from knowledge of the individual constituents The data given here is based on current knowledge and experience. This Safety Data Sheet describes the product interms of safety requirements and does not signify any warranty with regard to the product's properties .The data given here only applies when product used for proper application(s). The product is not sold assuitable for other applications-usage in such may cause risks not  mentioned in this sheet. Donot use for other application(s) without seeking advice from manufacturer

DISCLAIMER OF LIABILITY :The information in this SDS was obtained from sources which we believe are reliable. However, the information is provided without any warranty, express or implied, regarding its correctness. The conditions or methods of handling, storage, use or disposal of the product are beyond our control and may be beyond our knowledge. For this and other reasons, we do not assume responsibility and expressly disclaim liability for loss, damage or expense arising out of or in any way connected with the handling, storage, use or disposal of the product. This MSDS was prepared and is to be used only for this product. If the product is used as a component in another product, this MSDS information may not be applicable.