Coal Quality and Combustion Workshop

Class Outline

By Rod Hatt

 

 

Introduction

 

Introduction of attendees

Following the coal through the system

Please ask questions

 

Coal Formation

What is Coal - Fossilized Swamp

Initial formation

Coalification

 

Coal Rank

Peat

Lignite

Sub bituminous

Bituminous

Anthracite

 

Generally Lose

          Moisture

          Volatile

          Oxygen

Gain Btu/lb

 

Changes through the eons.

 

Impact of strata

          Water penetration

          Rock Type

          Faults

          Heat

          Partings verse separate coal seams

 

Sea water contains dissolved mountains and coal is activated carbon

 

Coal Mining

Methods

Surface

Deep

Out of seam dilution

Coal Washing and Drying

Transportation Impacts

 

Sampling coal and coal analyses

 

Sampling methods

          The Good, The Bad and the Ugly

 

Terms

 

Proximate – Moisture, ash, volatile, fixed carbon (by difference)

Short Prox – Moisture, ash, sulfur, Btu/lb

Ultimate – Moisture, ash, sulfur, + carbon, hydrogen, nitrogen,

oxygen (by difference)

 

As Received

Dry Basis, DB

Moisture Ash Free, MAF

Moisture Mineral Matter Free, MMMF

Dry Ash Free, DAF

 

DB=As Received/(1-(Moist/100))

 

MAF=DB/(1-(dry Ash/100))

or

MAF=As Rec./(1-((moist+ash)/100))

 

Coal Handling

 

Means many things to different people

Dust and pluggages and spontaneous combustion

No good prediction methods

 

Surface Moisture

Total

Surface

Inherent

Air dried and residual moisture

Equilibrium Moisture

 

Surface Moisture

0-4              Dusty

3-6              Okay

6+               Sticky

 

Soil Moisture meter

Other methods – Hand ball test, microwave,

Shear stress testing

 

Fines

What sizes are important?

          2x0, 3x0, ¼, #28, #60, #200

Hard to measure

Mining method impacts

Washed coal?

Hardgrove Grindability Index - HGI

Crushing impacts – hammer mill, roll, breaker

 

Clays and mineral matter

Clays

Soluble materials

 

Chemical additives

Work in lab

Application is critical

Plants like mechanical fixes

 

 

Spontaneous Combustion

Coal size and compacting

Moisture ash free MAF oxygen     

 

Self Heating Temperature  SHT

 

SHT min Co = 140- (6.6x MAF oxygen)

 

<70o           High potential

70-100       Medium

>100o         Low

 

 

Combustion

 

The three T’s in practice

 

                                 Time          Temp         Turbulence    Size

 

Stoker               Long          Med           Low               Big

 

Pulverized         Short         High           Med              Tiny

 

Cyclone             Short+       Very           High             Med

 

Fluid Bed           Med           Low           High             Med

 

Size the coal and add air!

 

 

Coal Reactivity

 

Volatile Matter - Lighter fluid on charcoal

Weight vs. Heating value of volatile

 

Volatile

Fuel Ratio, Fixed carbon / Volatile

MAF Oxygen

C/H

HGI fineness

 

Volatile per million Btu

Oxygen per million Btu

 

The Story of NOX

 

Wolf in sheep’s clothes, lower NOx means poorer combustion

 

Air verse Fuel formed NOX

 

Air is 79% molecular nitrogen, N2

N2 is quite stable

It is hard to burn N2

 

Coal is 0.5-2.0% nitrogen but,

N is not N2

Typical nitrogen bonding in coal could be, C-N=C

 

50-90% of NOX is formed from fuel nitrogen

 

To minimize the formation of NOx

 

Lower Oxygen

Lower Flame Temp

Lower Fuel Nitrogen

Increase fuel reactivity

 

Post Combustion Control

 

SCR = Selective Catalytic Reduction

 

NOX + NH3 w/catalyst = N2 + H2O

 

Catalyst can be poisoned by arsenic and fouled by CaSO4

 

NSCR does not use catalyst

 

Pulverizers

 

Coal fineness

Measurement

Coal properties

Surface moisture

HGI

Coal size

Heating value

  

HGI test is relative at best

  

Mill Wear

 

Not HGI

 

Ash levels

Types of minerals

Clays - soft

Pyrite - harder

Quartz - hardest

Sandstone

Pounds not percent

Use coal throughput

Coal type matters

  

Combustion Process

 

Coal Rank

Moisture and oxygen

Moisture Ash Free basis MAF

Volatile Matter

Lighter fluid on charcoal

Weight vs. Heating value

Hydrogen

HGI

Air to fuel ratios

Theoretical air

Excess air

Excess oxygen

Measurements

Performance testing

Duct coverage

Loss on ignition - LOI samples

Methods

Visual analysis

Air heater leakage

Balancing furnaces

Balancing burners

NOx formation

CO analysis

 

Boiler Efficiency

 

Boiler efficiency vs. excess oxygen

Moisture and hydrogen impacts

1% change for 10% moisture change

1% change for 1% hydrogen change

Higher vs. Lower heating value

 

Ash Deposits - Introduction

 

Ash deposits formed from the combustion of coal and other fuels have plagued the steam production industry from the start.  The ash fusion test has been around for over eighty years.  As steam plant size increased, so have the problems associated with ash deposits.  This workshop is designed to cover: 1) The basic types of deposits, 2) Causes of deposits, 3) Analytical procedures for resolving, or at least providing information about deposits and fuels, and 4)Deposit removal and reduction techniques.

 

This workshop is informally based so, please ask questions as they come up.

 

Types of Ash Deposits

 

There are two basic forms of ash deposits:  molten ash and alkali salts.  The molten deposits are called slag and occur primarily in the furnace area of the boiler.  The alkali salts generally occur in the convection or cooler portions of the boiler and duct work.  Mr. Hatt’s article titled “Fireside Deposits in Coal-Fired Utility Boilers”(1) provides a good description of the particulars concerning the location and nature of most ash deposits.

 

Wall Slag

 

Wall slag is the molten slag that builds up on the furnace walls.  Wall slag is shed naturally as boilers cycle through their load range.  It is usually controlled by soot blowers using air, steam and in some cases water as a removal medium.  Most boilers have some degree of wall slag and it does not necessarily cause problems.  In fact boilers that do not have enough wall slag due to a change to high fusion coal may have problems with maintaining steam temperatures.  Western coals may produce a thin wall slag that is hard to remove and yet causes problems due to its reflective nature.  Excessive wall slag leads to the following problems:

1.      Wall slag flows to bottom of furnace, cools and plugs the opening situated there.  The ash eventually bridges over, sealing off the outlet for bottom ash removal.

 

2.      Wall slag acts as an insulator and impedes heat transfer to the water wall.  This increases the furnace exit gas temperature (FEGT) and allows molten ash to deposit in the superheater and convection pass regions.

 

3.      Slag buildup around the burner regions, called eyebrows, interferes with the coal and air flow.  This type of buildup can cause damage to the burners, among other things.

 

Superheater Slag

 

Superheater slags are those molten deposits that form in the superheater and other convection sections of the boiler.

 

Convection Pass Fouling

 

Convection pass fouling is caused by the formation of alkali sulfates, primarily CaSO4 and Na2SO4, that bond the flyash together.  These types of deposits are usually associated with the use of Western coal.

 

Low Temperature Deposits

 

Low temperature deposits such as air heater pluggages and stack deposits are formed due to the condensation of sulfuric acid mixing together with the flyash to form an acid mud.

 

Causes of Ash Deposits

 

The main causes of ash deposits depend where you work.  If you work in steam plant operations the main cause is lousy coal, if your are a coal buyer the main cause is lousy steam plant design, and if you are in engineering the main cause is lousy steam plant operation.  All are right in a sense.  Scientific analytical investigations reveal that it is usually a combination of all three of these areas.

  

The following table presents the major causes of ash deposits:

 

TABLE I - Major Causes of Ash Deposits

 

 

Fuel Related

 

Large pyrite particles that impact the furnace wall before they completely combust.

 

Clay minerals that contain significant amounts of iron, calcium, sodium or potassium causing them to have low melting temperatures.

 

Interaction of pyrite, clays and alkalis with alumino silicates to form low viscosity melts

 

Extremely fine or organically bound alkalis

  

Equipment Related

 

Soot blowers not in operation or used improperly

 

Poor pulverization of fuel

 

Improper air to fuel ratio

 

Burners damaged or improperly adjusted

 

Changes in operation of boiler or other equipment

  

Design Related

 

Furnace size too small for fuel

 

Tube material and/or spacing inadequate

 

Soot blowing coverage inadequate

 

No means provided to observe slag buildup

 

 Analytical Procedures

 

Slag

 

Lets start our review with an overview of coal mineralogy and its relationship to coal ash chemistry, melting & slagging properties, and fusion temperature.  There are not distinct melting points for coal ash like with ice or other pure compounds, so when  melting is mentioned it is used to represent a decrease in viscosity, rather than a melting point.  When coal ash melts it occurs on both a large scale and a microscopic scale.  On the large or bulk scale the ash behaves like a glass.  As the temperature of the material increases, its viscosity decreases.  At temperatures less than 2000o F.  the ash may appear solid, or at least stiff, such as a Tootsie Roll.  On a microscopic scale several minerals may have all ready melted, but their concentrations are low when compared to other minerals with higher melting temperatures.  As the temperature is increased the ash becomes less viscous or more liquid like. Many reactions are now occurring between the minerals as they melt and become more fluid.  As the molten components mix they become more like molten glass.  This molten material starts to dissolve the non molten materials like quartz and other minerals.  In this way the melting temperature of minerals such as sandstones and shales are lowered by other minerals such as pyrite and limestone. 

 

The ASTM Fusion Temperature Test is a documented observation of this process occurring in coal ash shaped like a small cone, and placed in a furnace with increasing temperatures.  The initial deformation temperature, ID, is usually a hundred or more degrees above where the first low melting temp. minerals start to melt.  The remaining fusion temperatures represent an ever increasing amount of molten material, and a lowering of the viscosity of the glass like material.  It should be noted that even at the fluid temp. there may be solid or non-melted minerals such as quartz.  The atmosphere of the furnace is controlled to either an oxidizing (like air) or a reducing (CO present) condition.  This is important due to the oxidation behavior of iron (Fe) atoms.  Reduced iron lowers melting and fusion temperatures of ash much better than the oxidized form.  In coals that have significant iron levels, like those in the Illinois Basin, the oxidation state of the iron is critical.  The difference between the oxidizing and reducing fusion temps. can be hundreds of degrees.  This phenomenon is one of the variables that make consistent fusion temperature data hard to obtain.

 

When trying to determine the behavior of coal ash in a boiler, both the type and size of minerals present is important information.  Unfortunately it is both difficult and expensive to determine the actual minerals in coal.  The ash chemistry or major and minor elements in coal ash are the next most useful information.   This is because melting properties can be estimated and minerals can be inferred.  Although the cost of ash chemistry is higher than fusion tests, the information obtained is well worth the expense.  The fusion temperature test is a lower cost technique with reasonable turnaround time.  Fusion temperatures have been used for years, and are contained in most coal contracts.  Unfortunately,  fusion temps. provide no mineralogical information, are notoriously imprecise and are influenced by all sorts of factors that cause variability.  It is the authors experience that different laboratories can produce fusion temperatures that vary well outside the ASTM guidelines, and both laboratories are performing satisfactorily.

  

Ash levels

 

Ash levels in coal are generally reported from the lab as a percent of ash.  This is convenient for the lab but not completely representative of what the boiler sees.  Boilers demand Btus, not tons of fuel.  A more representative (for the boiler) way to express ash levels is to use pounds of ash per million Btu.  These units are easy to calculate using the following expression:

 

Lb. Ash/MBtu =  %Ash/(Btu/lb./10,000)

 

The author has on numerous occasions found that the ash deposits formed in utility sized boilers correlates best with ash and elemental loading data, rather than fusion temperatures or traditional slagging and fouling indices.

 

Elemental loading

Pounds of iron per million Btu

Pounds calcium, sodium, and other elements

 

Slagging with Bituminous Type Ash - High Iron

 

This example will show how a utility was able to lower its ash fusion specification by understanding how different coals behave in the boiler.  Typically utilities have specifications for total ash (in percent) and a fixed fusion temperature spec.  Published accounts of utilities experience in this area have led many slag specialists to consider the amount of ash loading to be important.  When ash levels are expressed in pounds per million Btus, they more closely reflect the levels seen by the boiler.  The author has also proposed that the Iron loading (lbs.Fe2O3/MBtu) level is an important consideration.  In several Eastern/ Midwest UScoal slagging events worked on by the author, the problematic coal had elevated iron loading levels.  Using this information several utilities have conducted test burns of coals with lower fusion characteristics.  Their strategy was to limit the iron loading by considering lower ash, higher iron coals.  These coals had lower than design fusion temperatures but it was suggested that the lower ash levels would offset this.  The results of the test confirmed that the iron loading levels more accurately predicted the slagging behavior of the coal than the fusion temperature of the coal.

 

Ash fusion temperatures

 

Ash fusion temperature tests have been around for almost a century.  At first there was just one, then three, and finally we know have four reported fusion temperatures.

 

Designed for stoker furnaces

Many deficiencies when used for evaluation of slagging or fouling deposits in pulverized coal furnaces.  The fact that the test can be run in both reducing and oxidizing conditions does provide clues about the role of combustion conditions on the mineral behavior.

 

Advanced ash fusion techniques have not grown in demand.

 

Ash Chemistry

 

Not Minerals, just oxides

 

Acids or glass formers

Silicon dioxide                         SiO2

Aluminum oxide                        Al2O3

Titanium dioxide                      TiO2

 

Bases or fluxing agents

Iron oxide                                Fe2O3

Calcium oxide                          CaO

Magnesium oxide                      MgO

Potassium oxide                       K2O

Sodium oxide                           Na2O

 

Base to acid ratio

Sum of bases/sum of acids

B/A vs. Fusion Temps.

 

Slagging index

Dry sulfur x B/A

Iron squared term

 

Computer Controlled Scanning Electron Microscopy provide some of the best mineralogical information but has not come into common use.

 

 

Fouling Deposits

 

Chemical Fractionation

Active alkali

Water soluble

Ammonium Acetate soluble

Weak acid soluble

Micro crystals

 

Cyclone  and Wet Bottom Furnaces

 

Each cyclone is individual furnace

Balanced air to fuel ratio

Must have wet slag to work

          Must be hot, maintain minimum loading

          Coal Sizing is important to good combustion

          Ash loading minimum

          Must be low fusion ash

Many don’t use fluid fusion temperature

T-250 temperatures

Temperature at which slag will flow

T-250 methods

T-250 vs. Heating value

 

Deposit Analyses

Proper Sampling (2)

Optical and Electron Microscopy

  

Electrostatic Precipitator

 

Basic Coal Chemistry

 

Moisture %

Ash %

Sulfur %

Btu/lb

 

Loading or how the boiler sees things

 

Pounds of material per million Btus (lbs./MBtu)

 

lbs. SO2/MBtu

lbs. Ash/MBtu  %Ash/(Btu/10,000)

 

ESP Operation

 

For given conditions and coal, ESP is constant efficiency.

More ash in = more ash out.

 

Opacity is dependent on many parameters including the size of material and the amount of material.

 

Temperature

Resistivity

Flow

 

Equipment

Controls

 

Rappers

 

Alignment

 

Flow vanes

Boiler Operation

 

Combustion

ESP used to collect ASH

Strong correlation between LOI and Opacity

 

Balancing the Boiler

How do your operators do it?

Oxygen

LOI and NOX issues

Temperature

Flow

                   Fan amps

                   Controls

                   Measured

 

Airheaters pluggage and leakage

 

Coal Chemistry

Change in slagging properties can change ESP loading

Mineral Mater in Coal

 

 

Chemistry review

Not Minerals, just oxides

 

Rocks, shales, clays

Silicon dioxide                SiO2

Aluminum oxide               Al2O3

Titanium dioxide             TiO2

 

Other Minerals

Pyrite FeS

Iron oxide                       Fe2O3

 

Organic, limestone, dolomite

Calcium oxide                 CaO

Magnesium oxide             MgO

Sodium oxide                  Na2O

 

Clays

Potassium oxide          K2O

 

Resistivity

 

Hot side

Cold side

 

Sodium

Sulfur Trioxide

 

Measuring

Calculating

 

 Opacity

Particle size

minerals verse condensation

 

Coal Specifications

 

Boiler design specifications

What you think you are going to burn

Boiler Data Sheet - guaranteed performance

 

Bid specifications

Don’t limit your options

Where can you be flexible

 

Contract specifications

Can you protect yourself

Use the right parameters

Penalties and premiums

 

Computerized Evaluations

 

Many important impacts can’t be accurately predicted

Coal quality information comes from many sources

Recent shipment

Core drilling

Average production over recent past

Typical or Made Up analyses

Use as a communication tool between interested parties

 

Test Burns

 

Computerized evaluations

Trial Burns

Test Burns

Coal Blending and test burns

 

Conclusion