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Boiler Water Treatment Chemicals, Feed, and Control - Perhaps It Is More Complicated Than We Thought
Boiler Water Treatment Chemicals, Feed, and Control - Perhaps It Is More Complicated Than We Thought
2Na2SO4
For the residual, 1.6 ppm Na2SO3 will yield 1 ppm SO3.
The total calculation equation to remove residual oxygen and provide a boiler water residual is:
(Feedwater O2 x 7.88) + (1.6 x Boiler Water SO3 Residual) / Feedwater Cycles
= Feedwater Dosage of 100% sodium sulfite in ppm.
Spreadsheets can be made as shown at the end of the paper that illustrate the impact of changes
in variables such as dissolved oxygen concentration, feedwater cycles, steam production, desired
sulfite residual, and applied dosages. Examine the results shown on the examples.
If the dissolved oxygen concentration varies from 0.01 ppm to 1.0 ppm in the feedwater, to
maintain the 30 ppm boiler water residual, the daily dosage demand increases by almost 500%
and the reaction demand increases from 3.9% of the dosage to 80%. Clearly a variable oxygen
content is very difficult and costly to control.
Looking at cycle control reveals that even though the dosage to obtain a residual may increase
dramatically at low cycles, only a small portion of the sulfite total dosage is required to remove
oxygen, so residual control is not as important if the deaerator is operating properly. The reaction
dosage at 5 to 50 cycles only varies from 0.8% to 7.6% of the total required dosage.
Changing the residual in the boiler if the deaerator is operating properly can change consumption
significantly, but should have little impact on results, unless the deaerator dissolved oxygen level
spikes above the 0.01 ppm level. Variations in deaerator oxygen removal obviously would have a
great impact on sulfite consumption. If the dosage is fixed at 1.92 ppm at 25 cycles, and the
oxygen content from the deaerator increases from 0.01 ppm to 0.1 ppm, the sulfite residual will
drop from 29 ppm to 18 ppm. The reaction demand increased from 4.1% of the total dosage to
41%.
Clearly, the control of sulfite feed and maintaining control will depend upon the specifics of each
system. A deaerator that provides consistent, low oxygen residuals will be much easier to control
than one that is giving unsteady results. Feedwater heaters with variable oxygen levels will be
nearly impossible to control economically. Where dissolved oxygen levels are high or variable
and when using feedwater heaters, applying a passivator such as erythorbate or DEHA would be
a valuable addition to the sulfite.
Sodium Hexametaphosphate
Sodium hexametaphosphate is a commonly used source of orthophosphate anion used to
precipitate calcium in low pressure boilers. With dispersants the calcium phosphate becomes a
fluidized sludge capable of being blown down and out of the boiler before the calcium can form
a deposit.
Example:
The reaction rate is the first part of the equation and the residual the second part:
[ (0.72 x Ca + 1.08 x PO4/ Feedwater Cycles) ]
= ppm of 100% sodium hexametaphosphate in feedwater.
Again, spreadsheets can be made varying calcium in the feedwater, cycles, steam load, changing
desired phosphate residuals, or holding the phosphate dosage constant.
Examining the spreadsheets reveals that if the feedwater calcium level is low, most of the
product dosage goes to provide residual in the boiler water. If the calcium level starts to become
significant, the reaction portion of the equation may become the major demand for the product.
Obviously, control will be difficult with variations in feedwater calcium just as with variation
with oxygen for sulfite control.
If the feedwater cycles are varied from 5 to 50 cycles, the dosage requirement changes by over a
factor of 8, with most of the demand coming from the residual portion of the calculation. So even
though residual may change significantly, if calcium is low and consistent, there is enough
phosphate to satisfy the demand, and calcium carbonate scale should be avoided even with wild
changes in blowdown rates.
Chelant Treatment
EDTA dosage requirements and variations will be similar to phosphate in that there is a reaction
and residual portion to the dosage calculation:
(Feedwater hardness) x (3.8) + ppm EDTA desired residual = ppm EDTA Product
% active
(feedwater cycles) x % active
100
100
Economical control would again be very difficult with fluctuations in feedwater hardness.
Looking at the spreadsheet at the end of the paper shows that the EDTA dosage demand can
easily increase twenty-fold with poor feedwater hardness control. Phosphate treatment would be
easier to control with variations in feedwater hardness.
Blended Products
The variation in phosphate demand or chelant demand and changes in cycles makes
phosphate/polymer or chelant/polymer blends difficult to control. These products are best
designed for a specific and consistent condition. A formulated product should be evaluated for
each system and anticipated fluctuations to see how the polymer level varies if phosphate or
EDTA is used as the control.
Example: A boiler product contains 10% EDTA and 15% polymer. It is applied to a boiler
operating at 20 cycles with 0.1 ppm feedwater hardness. Feedwater dosage is 8.8 ppm to yield 10
ppm free EDTA and 26 ppm polymer.
If the hardness goes up to 1 ppm or the product is used in another system where the hardness is 1
ppm, the feedwater dosage increases to 43 ppm to obtain 10 ppm free EDTA. This would yield a
high polymer level of 129 ppm. Polymer overfeed is expensive and high polymer levels can
cause boiler water carryover with their surface-active properties that occur at high
concentrations.
Other Chemical Feed and Control Considerations
How and where the various boiler chemicals are fed can affect their performance and control.
a. Oxygen scavengers are best fed to the storage section of the deaerator or feedwater tank.
In most low pressure industrial boiler systems, if oxygen remains in the feedwater and
enters the boiler, it is too late to remove all of the oxygen and protect the boiler and
condensate from oxygen corrosion. A residual of sulfite or other oxygen scavenger in the
boiler cannot chemically reduce all of the oxygen before it escapes with the steam or
reacts with the metal surfaces.
The oxygen scavenger should be pumped either continuously or paced with makeup into
the deaerator so that there is a positive residual at all times in the deaerator. Consideration
should be given to see where the makeup and condensate enter the deaerator. Often times
the high pressure condensate enters directly into the storage section. If the condensate
contains oxygen, intermittently high dissolved oxygen levels in the feedwater may occur.
Also sudden load changes can allow temporary high dissolved oxygen levels.
Even with sulfite feed to the deaerator, but especially if sulfite is fed to the boiler, the
boiler sulfite residual may not show a big change as oxygen is released into the steam or
corrodes the boiler before it is reduced chemically. Dissolved oxygen testing in the
feedwater would be the best tool to insure consistently low dissolved oxygen levels and
adequate chemical feed and control.
How condensate is returned, the level controls on the deaerator, and the proportion of
makeup to condensate can affect deaerator performance and therefore results. If there is a
relatively small deaerator volume and the amount of condensate return varies throughout
the day or night, load and performance can change. Dissolved oxygen content and
feedwater oxygen scavenger concentration should be checked under the changing
conditions.
These situations could explain why one system sees corrosion and another does not, even
though it appears to be the same treatment and control.
b. 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.
c. 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.
d. 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.
tubes right near the feedwater entry point. Dont assume there is not a corrosion problem based
upon inspecting only the top rows of tubes as seen from the manway. Check the area around the
feedwater entry point. The concern is greatest with feedwater heaters. I have seen sulfite
residuals well maintained in boilers with sulfite residuals in the feedwater, but corrosion on the
tubes immediately near the feedwater entry point. A continuous dissolved oxygen analyzer on
the feedwater revealed residual oxygen. Corrosion coupons in the feedwater showed pitting
corrosion in less than an hour.
The relatively cold feedwater containing residual hardness will fall to both ends of the boiler and
then rise. Initial precipitation of the minerals will occur here, which is also the hottest part of the
boiler. Scale and sludge deposition will most likely occur near the entry point and the high heat
area and sludge accumulation will concentrate in the ends of the boiler where the water is first
directed. Check for deposition on these lower tubers and on the bottoms of the tubes. Minimize
iron and hardness levels and use chelating agents.
Attemperation
As a rule, the water used for desuperheating steam should be the same quality as the steam. High
quality condensate or mixed bed demineralized water are good choices. It is common to see
boiler feedwater used if the quality is high since the boiler feedwater pump can be used to supply
the attemperation water, thereby reducing the expense of an additional pump. If feedwater is
used, chemicals added to the deaerator or feedwater before the attemperation take-off point
should be volatile. For FDA plants, erythorbate that is pH neutralized with amine is used.
Intermittent Boiler Water Carryover
Steam purity is the measurement of dissolved solids in the steam and steam quality is a
measurement of moisture content. Both watertube and firetube boilers can experience variances
in the degree of carryover based upon steam load and changes in load. Detecting carryover is not
always easy. Chemicals can contribute to foaming and priming in boilers. High total dissolved
solids along with high alkalinities are potential culprits. Oil and other contaminants can create
carryover. High polymer concentrations as stated earlier have been shown to cause problems.
Continuous or regular short interval testing of condensed steam may be necessary to catch
carryover as it may occur in short spurts. Moisture in the steam can lead to impingement on
steam lines and steam traps. Black iron deposits in traps and condensate receivers can be an
indicator of this problem. If intermittent carryover is occurring, see if the water level can be
lowered to correct the problem.
To determine if the applied chemicals are contributing to the problem, discontinue chemical feed
until all of it has been purged from the boiler and retest for carryover. A good test is to compare
sodium and silica in the boiler water to that in the condensed steam.
Summary
Chemical treatment of boilers and chemical selection should be based upon each individual
system. Similar programs can perform very differently depending upon the particular boiler
system and operation.
Theoretical usages and actual consumptions should regularly be compared and discrepancies
justified. The dosages and residuals for the range of situations expected for the system should be
calculated to determine what problems or concerns there may be and how well the program can
be controlled.
DO
0.01
0.05
0.1
0.5
1
Cycles
25
25
25
25
25
Steam lbs/day
1,000,000
1,000,000
1,000,000
1,000,000
1,000,000
Reaction Demand ppm Residual Dose ppm Total Dose ppm Daily lbs.
0.08
1.92
2.00
2.08
0.39
1.92
2.31
2.41
0.79
1.92
2.71
2.82
3.94
1.92
5.86
6.10
7.88
1.92
9.80
10.21
Dosage Proportions
% Reaction % Residual
3.9%
96.1%
17.0%
83.0%
29.1%
70.9%
67.2%
32.8%
80.4%
19.6%
Vary Blowdown
SO3 Residual
30
30
30
30
30
DO
0.01
0.01
0.01
0.01
0.01
Cycles
5
10
20
25
50
Steam lbs/day
1,000,000
1,000,000
1,000,000
1,000,000
1,000,000
Reaction Demand ppm Residual Dose ppm Total Dose ppm Daily lbs.
0.08
9.6
9.68
12.10
0.08
4.8
4.88
5.42
0.08
2.4
2.48
2.61
0.08
1.92
2.00
2.08
0.08
0.96
1.04
1.06
Dosage Proportions
% Reaction % Residual
0.8%
99.2%
1.6%
98.4%
3.2%
96.8%
3.9%
96.1%
7.6%
92.4%
Vary Residual
SO3 Residual
5
10
20
30
50
DO
0.01
0.01
0.01
0.01
0.01
Cycles
25
25
25
25
25
Steam lbs/day
1,000,000
1,000,000
1,000,000
1,000,000
1,000,000
Reaction Demand ppm Residual Dose ppm Total Dose ppm Daily lbs.
0.08
0.32
0.40
0.42
0.08
0.64
0.72
0.75
0.08
1.28
1.36
1.42
0.08
1.92
2.00
2.08
0.08
3.2
3.28
3.42
Dosage Proportions
% Reaction % Residual
19.8%
80.2%
11.0%
89.0%
5.8%
94.2%
3.9%
96.1%
2.4%
97.6%
Vary Steam
SO3 Residual
30
30
30
30
30
DO
0.01
0.01
0.01
0.01
0.01
Cycles
25
25
25
25
25
Steam lbs/day
250,000
500,000
750,000
1,000,000
2,000,000
Reaction Demand ppm Residual Dose ppm Total Dose ppm Daily lbs.
0.08
1.92
2.00
0.52
0.08
1.92
2.00
1.04
0.08
1.92
2.00
1.56
0.08
1.92
2.00
2.08
0.08
1.92
2.00
4.16
Dosage Proportions
% Reaction % Residual
3.9%
96.1%
3.9%
96.1%
3.9%
96.1%
3.9%
96.1%
3.9%
96.1%
Steam lbs/day
1,000,000
1,000,000
1,000,000
1,000,000
1,000,000
Reaction Demand ppm Residual Dose ppm Total Dose ppm Daily lbs.
0.08
0.40
0.48
0.50
0.08
0.88
0.96
1.00
0.08
1.84
1.92
2.00
0.08
2.80
2.88
3.00
0.08
3.76
3.84
4.00
Dosage Proportions
% Reaction % Residual
16.4%
83.6%
8.2%
91.8%
4.1%
95.9%
2.7%
97.3%
2.1%
97.9%
Steam lbs/day
1,000,000
1,000,000
1,000,000
1,000,000
1,000,000
Reaction Demand ppm Residual Dose ppm Total Dose ppm Daily lbs.
0.08
1.84
1.92
2.00
0.39
1.53
1.92
2.00
0.79
1.13
1.92
2.00
3.94
0.00
1.92
2.00
7.88
0.00
1.92
2.00
Dosage Proportions
% Reaction % Residual
4.1%
95.9%
20.5%
79.5%
41.0%
59.0%
100.0%
0.0%
100.0%
0.0%
Reaction Demand ppm Residual Dose ppm Total Dose ppm Daily lbs.
0.08
1.52
1.60
2.00
0.08
1.72
1.80
2.00
0.08
1.82
1.90
2.00
0.08
1.84
1.92
2.00
0.08
1.88
1.96
2.00
Dosage Proportions
% Reaction % Residual
4.9%
95.1%
4.4%
95.6%
4.1%
95.9%
4.1%
95.9%
4.0%
96.0%
Dosage Proportions
% Reaction % Residual
92.3%
7.7%
82.1%
17.9%
77.8%
22.2%
77.0%
23.0%
75.4%
24.6%
Reaction %
% of Total
80.0%
70.0%
60.0%
50.0%
40.0%
30.0%
20.0%
Residual %
10.0%
0.0%
0
0.5
1.5
2.5
D.O. ppm
18.0%
70
60
14.0%
50
12.0%
Dosage
10.0%
40
8.0%
30
6.0%
20
Reaction %
4.0%
10
2.0%
0.0%
0.00
Resulting Sulfite
Residual, ppm
% Reaction Dosage
16.0%
1.00
2.00
3.00
4.00
0
5.00
10
Steam lbs/day
1,000,000
1,000,000
1,000,000
1,000,000
1,000,000
Daily lbs.
0.42
0.81
2.40
4.38
8.33
Dosage Proportions
% Reaction % Residual
0.0%
100.0%
48.7%
51.3%
82.6%
17.4%
90.5%
9.5%
95.0%
5.0%
Vary Blowdown
EDTA Residual Hardness Cycles
10
0.5
5
10
0.5
10
10
0.5
20
10
0.5
25
10
0.5
50
Steam lbs/day
1,000,000
1,000,000
1,000,000
1,000,000
1,000,000
Daily lbs.
4.88
3.22
2.53
2.40
2.14
Dosage Proportions
% Reaction % Residual
48.7%
51.3%
65.5%
34.5%
79.2%
20.8%
82.6%
17.4%
90.5%
9.5%
Vary Residual
EDTA Residual Hardness Cycles
1
0.5
25
2
0.5
25
5
0.5
25
10
0.5
25
20
0.5
25
Steam lbs/day
1,000,000
1,000,000
1,000,000
1,000,000
1,000,000
Daily lbs.
2.02
2.06
2.19
2.40
2.81
Dosage Proportions
% Reaction % Residual
97.9%
2.1%
96.0%
4.0%
90.5%
9.5%
82.6%
17.4%
70.4%
29.6%
Vary Steam
EDTA Residual Hardness Cycles
10
0.5
25
10
0.5
25
10
0.5
25
10
0.5
25
10
0.5
25
Steam lbs/day
250,000
500,000
750,000
1,000,000
2,000,000
Daily lbs.
0.60
1.20
1.80
2.40
4.79
Dosage Proportions
% Reaction % Residual
82.6%
17.4%
82.6%
17.4%
82.6%
17.4%
82.6%
17.4%
82.6%
17.4%
Daily lbs.
2.00
2.30
3.00
3.50
4.00
Dosage Proportions
% Reaction % Residual
99.0%
1.0%
86.1%
13.9%
66.0%
34.0%
56.5%
43.5%
49.5%
50.5%
`
Vary Hardness; Constant EDTA Dosage
EDTA Residual Hardness Cycles
Steam lbs/day
48
0
25
1,000,000
39
0.1
25
1,000,000
1
0.5
25
1,000,000
0
1
25
1,000,000
0
2
25
1,000,000
Daily lbs.
2.00
2.00
2.00
2.00
2.00
Dosage Proportions
% Reaction % Residual
0.0%
100.0%
19.8%
80.2%
99.0%
1.0%
100.0%
0.0%
100.0%
0.0%
Daily lbs.
3.00
3.00
3.00
3.00
3.00
Dosage Proportions
% Reaction % Residual
79.2%
20.8%
70.4%
29.6%
66.7%
33.3%
66.0%
34.0%
64.6%
35.4%
Daily lbs.
10.00
10.00
10.00
10.00
10.00
Dosage Proportions
% Reaction % Residual
95.0%
5.0%
84.4%
15.6%
80.0%
20.0%
79.2%
20.8%
77.6%
22.4%
11
9.00
100.0%
8.00
90.0%
80.0%
7.00
Reaction %
6.00
70.0%
60.0%
5.00
Dosage
50.0%
4.00
40.0%
3.00
30.0%
2.00
% Reaction
Dosage, lbs/day
20.0%
1.00
10.0%
0.00
0.0%
0
0.5
1.5
2.5
Hardness, ppm
12
Calcium Cycles
0
25
0.1
25
0.5
25
1
25
2
25
Steam lbs/day
1,000,000
1,000,000
1,000,000
1,000,000
1,000,000
Reaction Demand ppm Residual Dose ppm Total Dose ppm Daily lbs.
0.00
1.30
1.30
1.35
0.07
1.30
1.37
1.43
0.36
1.30
1.66
1.73
0.72
1.30
2.02
2.10
1.44
1.30
2.74
2.85
Dosage Proportions
% Reaction % Residual
0.0%
100.0%
5.3%
94.7%
21.7%
78.3%
35.7%
64.3%
52.6%
47.4%
Vary Blowdown
PO4 Residual Calcium Cycles
30
0.5
5
30
0.5
10
30
0.5
20
30
0.5
25
30
0.5
50
Steam lbs/day
1,000,000
1,000,000
1,000,000
1,000,000
1,000,000
Reaction Demand ppm Residual Dose ppm Total Dose ppm Daily lbs.
0.36
6.48
6.84
8.55
0.36
3.24
3.60
4.00
0.36
1.62
1.98
2.08
0.36
1.30
1.66
1.73
0.36
0.65
1.01
1.03
Dosage Proportions
% Reaction % Residual
5.3%
94.7%
10.0%
90.0%
18.2%
81.8%
21.7%
78.3%
35.7%
64.3%
Vary Residual
PO4 Residual Calcium Cycles
5
0.5
25
10
0.5
25
20
0.5
25
30
0.5
25
50
0.5
25
Steam lbs/day
1,000,000
1,000,000
1,000,000
1,000,000
1,000,000
Reaction Demand ppm Residual Dose ppm Total Dose ppm Daily lbs.
0.36
0.22
0.58
0.60
0.36
0.43
0.79
0.83
0.36
0.86
1.22
1.28
0.36
1.30
1.66
1.73
0.36
2.16
2.52
2.63
Dosage Proportions
% Reaction % Residual
62.5%
37.5%
45.5%
54.5%
29.4%
70.6%
21.7%
78.3%
14.3%
85.7%
Vary Steam
PO4 Residual
30
30
30
30
30
Steam lbs/day
250,000
500,000
750,000
1,000,000
2,000,000
Reaction Demand ppm Residual Dose ppm Total Dose ppm Daily lbs.
0.36
1.30
1.66
0.43
0.36
1.30
1.66
0.86
0.36
1.30
1.66
1.29
0.36
1.30
1.66
1.73
0.36
1.30
1.66
3.45
Dosage Proportions
% Reaction % Residual
21.7%
78.3%
21.7%
78.3%
21.7%
78.3%
21.7%
78.3%
21.7%
78.3%
Reaction Demand ppm Residual Dose ppm Total Dose ppm Daily lbs.
0.36
0.12
0.48
0.50
0.36
0.60
0.96
1.00
0.36
1.56
1.92
2.00
0.36
2.52
2.88
3.00
0.36
3.48
3.84
4.00
Dosage Proportions
% Reaction % Residual
75.0%
25.0%
37.5%
62.5%
18.8%
81.3%
12.5%
87.5%
9.4%
90.6%
`
Vary Calcium; Constant Phosphate Dosage
PO4 Residual Calcium Cycles
Steam lbs/day
44
0
25
1,000,000
43
0.1
25
1,000,000
36
0.5
25
1,000,000
28
1
25
1,000,000
11
2
25
1,000,000
Reaction Demand ppm Residual Dose ppm Total Dose ppm Daily lbs.
0.00
1.92
1.92
2.00
0.07
1.85
1.92
2.00
0.36
1.56
1.92
2.00
0.72
1.20
1.92
2.00
1.44
0.48
1.92
2.00
Dosage Proportions
% Reaction % Residual
0.0%
100.0%
3.8%
96.3%
18.8%
81.3%
37.5%
62.5%
75.0%
25.0%
Dosage Proportions
% Reaction % Residual
22.5%
77.5%
20.0%
80.0%
18.9%
81.1%
18.8%
81.3%
18.4%
81.6%
Dosage Proportions
% Reaction % Residual
60.0%
40.0%
53.3%
46.7%
50.5%
49.5%
50.0%
50.0%
49.0%
51.0%
Calcium Cycles
0.5
25
0.5
25
0.5
25
0.5
25
0.5
25
13
4.00
70.0%
3.50
60.0%
3.00
50.0%
Dosage
2.50
40.0%
2.00
30.0%
1.50
Reaction %
20.0%
1.00
0.50
10.0%
0.00
0.0%
0
0.5
1.5
2.5
Reaction %
Dosage, lbs/day
3.5
Calcium, ppm
14