Background of the Invention
[0001] The invention relates to a process that increases the output of a combustor fired
with coal having high iron and/or calcium content, by reducing the tendency of slag
to form on heat exchange surfaces, changing the nature of the slag to make it easier
to remove and actually removing slag.
[0002] Combustion of coal, like other fossil fuels, is invariably less efficient than desired
and can be a source of pollution. Maintaining combustor operation at high efficiency
and controlling the quality of the emissions is essential for maintaining the energy
needed to power our economy while preserving the quality of the air we require for
survival. Because efficiency and emissions are interrelated and some technological
solutions have been shown to be competitive with each other, it has been difficult
to achieve both. Economic operation of power plants and incinerators is in the public
interest, and new technologies are essential to this effort.
[0003] Fuel selection plays an important role in mitigating some pollution problems, but
it cannot eliminate them. Some coals, such as certain Appalachian and Illinois Basin
bituminous coals, are important in many plants designed for coal where economics limits
other options. The tendency to form slag and the properties of the slag for such high
iron content coals have been a major concern of combustion engineers and plant operators
for decades. There are a number of factors that impact the physical and chemical properties
of slag. See, for example, Combustion Fossil Power, 1991, Joseph G. Singer, P.E.,
editor, Chapter 3, Combustion Engineering. However, as the industry stands today,
there is a compromise between selection of low-cost coal and the actual economics
of energy production where slagging becomes a problem. Slag accumulation is a problem
that causes decreased heat transfer and often leads to long periods of downtime for
cleaning.
[0004] An interrelated problem with coal is that large amounts of ash and fine particulates
are formed that must be captured and disposed of. The art has used additives to control
slag formation and properties, but the additives can stress the solids recovery systems
employed in terms of sheer volume. Accordingly, optimum slag control has often been
compromised because the solids recovery system could not effectively remove all of
the solids necessary. This is especially a problem with older plants where increasing
the solids collection capacity is not an option.
[0005] Making the problem more complex is the fact that coals react differently to additives
as a function of their composition. As a general rule, there are no known formulae
that make it possible to address all different coal compositions with suitable additives
at effective levels that can be adequately handled by solids recovery equipment. The
discovery of individual coal composition and additive regimens are highly sought after
to assure that economical power can be supplied while generating sufficient revenues
for effective pollution control.
[0006] US 4,498,402 describes a method for reducing high temperature slagging in furnaces and a conditioner
fo use therein.
[0007] US 2006/0121398 A1 deals with an additive atomizing system for injection into severe operating environments.
[0008] There is a need for an improved process that more effectively control slagging, especially
with problem fuels, such as coals with sulfur contents that cause them to play an
increased role in slagging and also those having high iron and/or calcium contents,
to improve boiler efficiency and economics.
Disclosure of Invention
[0009] It is an object of the invention to provide an improved technology for slag control
in combustors utilizing fuels tending toward the production of slag.
[0010] It is another object to provide a process to control slag from the combustion of
coal with high iron and/or calcium contents while reducing chemical utilization.
[0011] It is another object to provide a process to remove slag from boiler heat exchange
surfaces due to the combustion of coal with high iron and/or calcium contents while
reducing chemical utilization.
[0012] A yet further but more specific object is to provide a process to more effectively
control slag by decreasing the amount of downtime associated with slag removal.
[0013] It is a more specific object of some aspects of the invention to achieve the above
objects while at the same time improving combustor efficiency.
[0014] These and other objects are achieved by the present invention in at least its preferred
aspects which provides an improved process for slag control in combustors burning
slag-forming coal with high iron and/or calcium content.
[0015] In one aspect, the invention provides a process for reducing slag cohesiveness and/or
adhesiveness in a combustor, thereby decreasing the rate of fouling as defined in
the claim.
[0016] The aluminum trihydroxide reagent is introduced in the form of an aqueous liquid
and computational fluid dynamics is employed to determine flow rates and select reagent
introduction rates, reagent introduction location(s), reagent concentration, reagent
droplet size and/or reagent momentum.
[0017] Magnesium hydroxide is introduced as an aqueous slurry along with the slurry of aluminum
trihydroxide.
[0018] Other preferred aspects and their advantages are set out in the description which
follows.
Brief Description of the Drawings
[0019] The invention will be better understood and its advantages will become more apparent
when the following detailed description is read in conjunction with the accompanying
drawings, in which:
Fig. 1 is a schematic view of one embodiment of the invention.
Fig. 2 is a photograph of a slag sample obtained after operation for 24 hours of aluminum
trihydroxide into a combustor operated on a high iron content coal as set out in Example
2 below.
Detailed Description of the Invention
[0020] Reference will first be made to
Fig. 1, which is a schematic view of one embodiment of the invention.
Fig. 1 shows a large combustor
10 of the type used for producing steam for electrical power generation, process steam,
heating or incineration. Coal is fed by burners
20 and
20a and burned with air in a combustion zone
21. It is an advantage of the invention that coal that is high in iron (e.g., iron contents
of greater than 15%, e.g., from 20 to 35%, based on the weight of the ash and expressed
as Fe
2O
3) and/or calcium content (e.g., calcium contents of greater than 5%, e.g., from 10
to 25%, based on the weight of the ash and expressed as CaO). It is also an advantage
of the invention that slag can be effectively controlled even for coals having significant
sulfur contents, e.g., above 1% and in the range of from 3 to 5%. Here, and throughout
this description, all parts and percentages are by weight.
[0021] Air for combustion, supplied by fan
22 and ductwork
24, is preferably preheated by a gas-to-gas heat exchangers (not shown) which transfer
heat from ductwork (not shown) at the exit end of the combustor. Hot combustion gases
rise and flow past heat exchangers
26, which transfer heat from the combustion gases to water for the generation of steam.
Other heat exchangers, including an economizer (downstream and not shown) may also
be provided according to the design of the particular boiler. Slag left untreated
would tend to form on these heat exchanger surfaces, which are positioned within specific
combustors based on design considerations important to individual locations. It is
an advantage of the present invention that modeling techniques, such as computational
fluid dynamics, are employed to initially direct treatment chemicals (especially,
those identified as effective for particular types of coal according to the invention)
to the optimum locations for reducing and/or controlling slag buildup and maintaining
efficient operation of the boiler.
[0022] A series of suitable, preferably air assisted atomizing, nozzles in each of nozzle
banks
30 and
30a are provided for introducing aluminum trihydroxide with magnesium hydroxide slurry
from vessels
40 and
40a respectively. Both the ATH and the magnesium hydroxide are aqueous slurries. Supply
lines (e.g.,
41) are shown as double lines in the drawing. Valves (e.g.,
42) are represented by the common symbol (

), and temperature sensors (e.g.,
44) are represented by the common symbol (

). Both valves
42 and temperature sensors
44 are connected to controller
46 via electrical leads (e.g.,
48) shown in dotted lines. These valves, temperature sensors and leads are illustrative
only, and the skilled worker using the principles outlined herein will place them
strategically to provide appropriate control signals and responses. The controller
46 can be a general purpose digital computer programmed in accord with a predetermined
control regimen with both feed forward and feedback features.
[0023] Aluminum trihydroxide (Al(OH)
3), which has been found effective according to the invention for greatly lessening
the deposition of slag or cleaning deposited slag from troublesome coal types, is
also known under other names such as ATH, aluminum hydroxide and hydrated alumina.
Regardless of the form of aluminum trihydroxide raw material, it is preferred that
it is mixed with water for introduction from tank
40 through associated lines
41, with or without chemical stabilizers, to concentrations suitable for storage and
handling,
e.g., at least 25%, and preferably at least 65%, solids by weight.
[0024] As will be described, the concentration and flow rates will be initially determined
by modeling to assure that the proper amount of chemical is supplied to the correct
location in the combustor in the correct physical form to achieve the desired results
of reduced slagging and ease of clean up. For use in the process, it is diluted as
determined,
e.g., by computational fluid dynamics (CFD) to within the range of from 0.1 to 10 %,
more narrowly from 1 to 5 %. When the aqueous aluminum trihydroxyde contacts the hot
gases in the combustor, it is believed to be reduced to very small particles,
e.g., nano-sized particles,
e.g., under 200 nanometers and preferably below 100 nanometers. Median particle sizes
of from 50 to 150 nanometers are useful ranges for the process of the invention. To
approach this size, it is important that the ATH be introduced with water. The small
particles are believed to disrupt the normal crystalline or glass that forms the slag.
Regardless of the mechanism involved it is a distinct advantage of the invention that
the slag that does form is highly friable and breaks easily with brushing and can
be crushed by hand.
[0025] It is a significant advantage of the invention that the friability of slag that is
formed is increased, making it easier to remove. The invention also slows or eliminates
the buildup of slag. Advantageously, at high doses, the invention can actually remove
slag that has already formed. By the term "increase the friability of the slag" it
is meant that the slag after treatment requires less force per unit area to crush
than slag formed under the same conditions without the treatment. By the term "remove
slag" it is meant that the weight of the slag adhering to boiler, particularly heat
exchange, surfaces is reduced from initial values by the treatment of the invention.
There are several additional and attendant advantages of the invention, including
the reduction of SO
3 for high sulfur coals, the reduction of the pressure drop across heat exchange apparatus,
the ability to use lower cost coal, lower CO generation, lower CO
2 generation due to increased fuel consumption, better heat transfer, less down time,
higher throughput, cleaning on line, cleaner heat exchange surfaces, ability to clean
the whole combustor, and the ability to run at all loads with greater efficiency.
[0026] The process for most coals works best with a combination of ATH and magnesium hydroxide.
While some coals,
e.g., with low silicate compositions can be burned with reduced problems attributed to
slag, the use of magnesium hydroxide, at least initially, is preferred. The magnesium
hydroxide reagent can preferably be prepared from brines containing calcium and other
salts, usually from underground brine pools or seawater. Dolomitic lime is mixed with
these brines to form calcium chloride solution and magnesium hydroxide which is precipitated
and filtered out of the solution. This form of magnesium hydroxide can be mixed with
water, with or without stabilizers, to concentrations suitable for storage and handling,
e.g., from 25 to 65% solids by weight. For use in the process, it is diluted as determined
by computational fluid dynamics (CFD) to within the range of from 0.1 to 10%, more
narrowly from 1 to 5%. When it contacts the effluent in combustor, it is believed
reduced to nano-sized particles,
e.g., under 200 nanometers and preferably below 100 nanometers. Median particle sizes
of from 50 to 150 nanometers are useful ranges for the process of the invention. Other
forms of MgO can also be employed where necessary or desired,
e.
g., "light burn" or "caustic" can be employed where it is available in the desired
particle size range.
[0027] To best achieve these effects, the invention will preferably take advantage of CFD
to project initial flow rates and select initial reagent introduction rates, reagent
introduction location(s), reagent concentration, reagent droplet size and reagent
momentum. CFD is a well understood science, and it is utilized with full benefit in
this case, where it is desired to supply a minimum amount of chemical for maximum
effect.
[0028] It is noted as highly significant that the amount of chemical will be substoichiometric
in terms of affecting the fusion point of the slag - often considered to be the controlling
factor in slag control. According to the present invention, there is good evidence
besides the relatively small amount of reagent employed that the results of the invention
are due to a physical disruption of slag formation with possible boundary chemical
and kinetic effects not explained by the literature.
[0029] Testing has shown that initial feed rates determined by CFD can be utilized with
good effect and then adjusted based on observed results. As a guide to feed rates,
the initial feed rate for the best economics for combustors operating similar to the
one exemplified below can be up to 2.7 kg (6 pounds) of ATH(as dry active ATH) or
3.6 kg (8 pounds) (as a 65-70% slurry) per ton of coal. For example, when added as
a preferred 70% slurry, amounts of from 0.45 to 2.7 kg (1 to 6 pounds) of slurry will
be effective (more narrowly,
e.g., 0.9 to 1.36 kg (2 to 3 pounds) of slurry). Also used are up to 0.9 kg (2 pounds)
of Mg(OH)
2 slurry (at about 50 - 60 % solids) per ton of coal. For example, when added as a
preferred 60% slurry, amounts of from 0.23 to 0.9 kg (0.5 to 2 pounds) of Mg(OH)
2 slurry per ton of coal,
e.g., from 0.3 to 0.45 kg (0.7 to 1 pounds) of Mg(OH)
2 slurry per ton of coal can be utilized. The slurries are diluted as necessary, typically
to a solids concentration of from about 5% for smaller applications to 35% or more.
[0030] The weight of the slag adhering to a combustor, particularly heat exchange, surfaces
is effectively reduced from initial values by the treatment of the invention, especially
when the ATH and Mg(OH)
2 are used at high concentrations within the above ranges, i.e. from 1.36 to 2.7 kg
(3 to 6 pounds) of ATH per ton of coal and 0.45 to 0.9 kg (1 to 2 pounds) of Mg(OH)
2 per ton of coal. This ability to remove slag provides the ability to provide a cleaning
and maintenance regimen wherein the initial dosing is as just mentioned for removing
slag, with the dosing then reduced to from 10 to 50% of the initial values for maintaining
the combustor clean and operating efficiently.
[0031] It is essential for optimum slag remediation according to the invention, that the
correct initial concentrations, rates and introduction rates be calculated and employed
for the effective physical form of aluminum trihydroxide, and preferably, optionally
magnesium hydroxide, to be introduced into the hot combustion gases in chamber
20 to enable the chemical to be added with the desired effect. The implementation of
CFD to the invention can be accomplished as set out in
U. S. Patent No. 7,162,960 to Smyrniotis, et al. Particulate removal equipment (not shown) can be employed to remove particulates
prior to passing the effluent up the stack.
[0032] In another alternate form of the invention, combustion catalysts and or effluent
treatment chemicals can be added to the fuel, combustion zone or otherwise as described,
for example in
U. S. Patent No. 7,162,960 to Smyrniotis, et al.
[0033] The following examples are presented to further explain and illustrate the invention
and are not to be taken as limiting in any regard. Unless otherwise indicated, all
parts and percentages are by weight.
Example 1 (not within the claim)
[0034] This example illustrates introduction of aluminum trihydroxide into a furnace burning
540 tons of coal per day. The coal is a blend of Illinois basin and Appalachian bituminous
coals, giving the following analysis as combined:
| Sample |
| |
1 |
2 |
3 |
| Moisture, % |
11.28 |
10.85 |
10.19 |
| Ash, % |
14.91 |
13.63 |
13.91 |
| Volatile Matter, % |
|
36.03 |
35.04 |
| Fixed Carbon, % |
|
39.49 |
40.86 |
| Total, % |
|
100 |
100 |
| Sulfur, % |
|
3.95 |
4.44 |
| HHV, BTU/lb |
|
10,742 |
10,730 |
[0035] For the test Al(OH)
3 (aluminum trihydroxide slurry or ATH for short) is fed as a 70% by weight aqueous
slurry at a rate of 2.3 kg (5 pounds) slurry per ton of coal consumed from two banks
of three air-cooled nozzles positioned on the wall opposite of two banks of pulverized
coal burners - one bank at an elevation between the two burners and one bank at an
elevation above the uppermost coal burners. The slurry is diluted to a concentration
of 35 weight % ATH. The density of the ATH slurry before dilution is 6.3 kg/3.8 1
(14 pounds/gallon), meaning that the feed rate is 730.6 1 (193 gallons) per day (2.3
kg (5 pounds) per ton of coal) for ATH slurry.
[0036] Based on this test, it is estimated that an effective feed rate for this particular
combustor will be from 0.45 to 2.7 kg (1 to 6 pounds) of ATH slurry per ton of coal,
e.g., 0.9 to 1.36 kg (2 to 3 pounds) per ton.
Example 2
[0037] This example illustrates the effect of introducing Mg(OH)
2 (magnesium hydroxide) into a furnace burning 540 tons of coal per day in addition
to the aluminum trihydroxide fed in Example 1. The coal was a blend of Illinois basin
and Appalachian bituminous coals, as illustrated in Example 1.
[0038] The magnesium hydroxide was fed as a slurry at 0.9 kg (2 lbs) of 50 to 60 weight
% slurry per ton of coal consumed. Density of the magnesium hydroxide slurry was approximately
5.4 kg/3.8 1 (12 lbs/gallon). Therefore, the feed rate was about 340.7 1 (90 gallons)
per day for the Mg(OH)
2 slurry. As before, we fed the aluminum trihydroxide slurry at 2.3 kg (5 pounds) of
slurry per ton of coal consumed. The density of the ATH was 6.3 kg/3.8 1 (14 pounds/gallon),
making the feed rate 730.6 1 (193 gallons) per day for ATH.
[0039] Based on this test, we estimate optimal feed rate for the best economics for the
this particular combustor to be 0.23 to 0.9 kg (0.5 to 2 pounds) Mg(OH)
2 slurry per ton of coal (e.g., 0.45 kg (1 pound) per ton) plus from 0.45 to 2.7 kg
(1 to 6 pounds) ATH slurry per ton (e.g., 0.9 to 1.36 kg (2 to 3 pounds per ton).
Fig.
2 is a photograph of a slag sample obtained after operation for 24 hours of ATH feed
only. The slag was unexpectedly friable.
[0040] The above description is for the purpose of teaching the person of ordinary skill
in the art how to practice the invention. It is not intended to detail all of those
obvious modifications and variations, which will become apparent to the skilled worker
upon reading the description. It is intended, however, that all such obvious modifications
and variations be included within the scope of the invention which is defined by the
following claim. The claim is meant to cover the claimed components and steps in any
sequence that is effective to meet the objectives there intended, unless the context
specifically indicates the contrary.