treatment of solid waste
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Note: The source of the technical material in this volume is the Professional
Engineering Development Program (PEDP) of Engineering Services.
Warning: The material contained in this document was developed for Saudi
Aramco and is intended for the exclusive use of Saudi Aramcos
employees. Any material contained in this document which is notalready in the public domain may not be copied, reproduced, sold, given,
or disclosed to third parties, or otherwise used in whole, or in part,
without the written permission of the Vice President, Engineering
Services, Saudi Aramco.
Chapter : Environmental For additional information on this subject, contact
File Reference: ENV10202 K. Hibrawi on 873-0211
Engineering EncyclopediaSaudi Aramco DeskTop Standards
Treatment of Solid Waste
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CONTENTS PAGES
METHODS OF PHYSICAL TREATMENT OF SOLID WASTE......................... 1
Manual Separation.......................................................................................6
Mechanical Separation ................................................................................ 6
Density.............................................................................................7
Optical............................................................................................10
Magnetic ........................................................................................ 10
Screening................................................................................................... 11
Vibratory Screens .......................................................................... 11
Rotary Screen.................................................................................12
Disc Screen .................................................................................... 12
Shredding .................................................................................................. 12
Mills...............................................................................................13
Shears.............................................................................................13
Grinding .................................................................................................... 15
Tubs ............................................................................................... 15
Mills...............................................................................................16Baling ........................................................................................................ 16
Example Problem 1. Volume reduction by materials separation
and recovery of recyclables...................................... 17
Filtration .................................................................................................... 19
Filter beds ...................................................................................... 19
Drums ............................................................................................ 19
Presses............................................................................................20
Flocculation...............................................................................................21
Precipitation...............................................................................................21
Flotation .................................................................................................... 22
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Evaporation ............................................................................................... 22
Ponds ............................................................................................. 22
Drying Beds ................................................................................... 23
METHODS OF CHEMICAL TREATMENT OF SOLID WASTE...................... 27
Oxidation................................................................................................... 28
Reduction .................................................................................................. 29
Neutralization ............................................................................................ 29
Calcination.................................................................................................31
Ion Exchange.............................................................................................31
Other Chemical Methods........................................................................... 32
LANDFARMING AND COMPOSTING AS SOLID WASTE
TREATMENT METHODS .................................................................................. 34
THERMAL DESTRUCTION METHODS OF SOLID WASTE TREATMENT. 41
Incineration................................................................................................41
Pyrolysis.................................................................................................... 58
Emerging Technologies............................................................................. 58
Microwaving..................................................................................58
Plasma Arc.....................................................................................59
SOLIDIFICATION AND STABILIZATION AS SOLID WASTE
TREATMENT METHODS .................................................................................. 60
Cement-Based ........................................................................................... 61
Thermoplastic-Based.................................................................................63
Silicate-based.............................................................................................65
Vitrification ............................................................................................... 66
GLOSSARY ......................................................................................................... 68
REFERENCES...................................................................................................... 69
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METHODS OF PHYSICAL TREATMENT OF SOLID WASTE
The primary purpose of physical treatment methods is to reduce the total quantity of solid
waste that requires disposal. This reduction in weight and/or volume can be accomplished by
one, or a combination of the following methods:
Manual separation
Mechanical separation
Screening
Shredding
Grinding
Baling
Filtration
Flocculation
Precipitation
Flotation
Evaporation
Source separation in many cases will result in less overall processing of waste and in therecovery of a higher quality product. Removing materials such as glass from the source
stream will reduce incinerator maintenance problems. The high thermal temperatures of
incinerators can actually melt glass. The molten glass then causes airflow through the
incinerator to decrease; this reduced airflow adversely affects combustion.
Figures 1 through 4 illustrate possible flow diagrams for the separation and recovery of
selected materials from commingled and source-separated municipal solid waste. All these
systems use a variety of the physical methods listed above. All the designs would be
improved by the addition of weighing scales throughout the process. It is essential to know
what materials are entering the plant and also to know the recovery efficiencies for the sorting
processes.
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Bagged
commingled
recyclable
materials
Second stage
manual sorting
Conveyer
Oversized material
Conveyor
Magnetic
separation
Conveyor
Conveyor
Screening
(trommel or disc)
Conveyor
First stage
manual sorting
Inclined conveyor
Bag breaker
Second-stage
manual presorting
Front-end loader,
floor and inclined
conveyor system
First-stage
manual presorting
Receiving areaFront-end loader
used to spread
waste for
presorting
Collection vehicle
Commingled MSW
Cardboard
Source-separated materials
in see-through bags
Bulky items
White goods
Other contaminants
Conveyor
Shredding
Combustion Compost for
intermediate landfill coverLandfill
Truck
Ferrous
metals
Paper
Plastics
Glass
Aluminum cans
Tin cans
Collection
vehicle
Source-separated
materials
Cardboard
Other large items
Paper
Cardboard
Plastics
Glass
Aluminum cans
Tin cans
Flow diagram for the separation and recovery of selected materials from commingledmunicipal solid waste
Figure 1
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Shipping
Forklift
Glass crusher
Forklift
Glass crusher
Mixed glass conveyor
Vibrating screen
Manual sorting
Conveyor
Conveyor
Manual sorting
Conveyor
Receiving hopper
Collection vehicle
Commingled
plastic and glass
Residual
materials
to landfill
Clear glass
crushed for
storage
Plastics
separated
accordingto type
Flow diagram for the separation and recovery of source separated waste: commingled glass
and plasticFigure 3
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Shipping
Forklift
Storage of baled
or crushed cans
Baler or
can crusher
Pulley magnet
Aluminum cans
Overhead magnetic
Conveyor
Conveyor
Receiving hopper
Collection vehicle
Commingled
aluminum and tin cans
Forklift or
pneumatic
conveyor
Tin cans,
baled or
crushed
Tin cans,
baled or
crushed
Flow diagram for the separation and recovery of source-separated waste: aluminum and steel
(tin) cans
Figure 4
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Manua l Separ ation
Manual separation of solid waste can either be accomplished at the source (for example, at the
home) or at a central collection station. "Curbside collection" at the home has the primary
advantage of eliminating the resident's need to drive to a central collection point.
Some cities provide multiple containers for the homeowner to sort the waste by types, such as
glass, plastic, paper and wet garbage. This separation process minimizes the labor of the
sanitation employees, but waste generators may not like the extra sorting effort. A second
method of curbside recycling is for the city to provide only a single recyclable waste
container. The homeowner bags wet garbage, or other materials the city cannot recycle,
separately. The waste collector performs the sorting of the recyclables at the time of the
pickup. The frequency of waste collection will help to determine if sanitation workers will
agree to this method of collection. A once-per-week collection frequency makes hand
sorting of garbage an undesirable activity. Concern for the possibility of transmittingcommunicable disease is another negative for handsorting.
Manual separation can be undertaken at a central collection point called a Materials Recovery
Facility (MRF). Waste generators can bring the waste to the MRF and do most of the sorting
by placing the material in separately marked bins. Another method is to have the sanitation
workers do the sorting at the MRF. The Rolla, Missouri MRF uses a combination of these
methods. Wastes at the Rolla MRF are placed in separate bins by the waste generators. Bins
are available for paper, plastic milk jugs, other plastics, glass (by color), aluminum and other
metals. Sanitation workers then ensure the sort has been done correctly, remove colored milk
caps (that can't be locally recycled) and prepare the sorted wastes for further processing steps.
If the bulk of the waste separation is performed by the sanitation workers, the MRF will often
have a conveyor belt system that brings the unsorted waste past a worker, who then removes
the recyclable materials as the waste passes the worker's station. These conveyor systems
haven't changed in concept since the turn of the century. The worker's protective equipment
has increased, and the conveyor facilities are now mostly air conditioned for worker comfort
and odor/pest control.
Mechanical Separ ation
Materials can be sorted by their physical properties: density (to sort light and heavy fractions);
optical clarity ( to sort glass or plastic by color); and electrostatic charge/magneticpermeability (to separate ferrous and non-ferrous metals).
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Density
Density separation can divide wastes into light fractions (such as paper, plastics and organics)
and heavy fraction (such as metals, wood and other heavy inorganic materials). Air
classification is the most popular of the methods, but devices called stoners and heavy media
separators are also used. A technology that is called "flotation" will be discussed in another
section.
In an air classifier, as shown in Figure 5, refuse enters the upper part of a chamber with air
blowing into the chamber from below. If the upward air velocity is high enough to overcome
the force of gravity on the particle, the particle will rise; small, heavy particles will fall to the
bottom of the chamber. Components suspended in the air stream are called "air classified
light fraction." Materials that settle out of the air stream are called "air classified heavy
fraction." Paper and plastics will concentrate in the light fraction, causing the light fraction to
have a higher heating value than the heavy fraction.
Unfortunately, air classifiers are sensitive to drag forces on the irregularly shaped particles.
Spherical particles are collected at different efficiencies than are flat particles of the same
weight and density. The more uniform the feed waste is the more consistent will be the
collection efficiency. Air classifiers are also sensitive to moisture content, which is absorbed
differently by various waste materials. Wet paper tends to stick together and will attract dirt .
The larger, relatively light paper fraction will carry into the light fraction with its load of dirt.
Shattered glass from a hammer mill can become imbedded in the paper and carry into the
light fraction.
A variation of the air classifier is called the air knife (shown in Figure 6). The device workswell with a waste stream that has already undergone some separation. The air current carries
paper and plastic with the air, while heavier materials fall more directly. Another density
classifying variation, known as a stoner, is shown in Figure 7. Air blows through a porous
deck and separates the material by differences in terminal velocity. Stoners work well over a
relatively narrow size range.
So-called heavy media separators have found popularity in the automobile recovery industry.
A pre-shredded feedstock with a high aluminum percentage is placed in a liquid with a high
specific gravity. The aluminum floats on the liquid, and the higher density materials settle or
remain below the surface.
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Heavyfraction
Ajustablebaffle
Ajustablebaffle
ShreddedrefuseLight fraction
Schematic of the air classification concept
Figure 5
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Air KnifePlenum
Refuse
Air from fan
Heavy
material
Light
material
Schematic of an air knife
Figure 6
Discharge
of light
material
Uniform supply
of fluidizing air applied
below porous deck
Porous deck sloped(about 4 ) and
vibrated in a
straight line
reciprocating motion
o
Light material that
is suspended and stratified
floats downslope
Light and heavy
materials to be
separated
Heavy material that
sinks to the bottom of
stratified bed
is conveyed upslope
by the deck's vibration
Discharge
of heavy
material
Schematic of a stoner
Figure 7
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Optical
Optical separation was popular in the 1970s and 1980s, but has fallen out of favor and is
rarely mentioned in current texts. The optical sensors were intended to sort glass by color, but
the sensors proved unreliable because the glass was frequently dirty or because the labels on
the glass interfered with the device that measured the optical properties. An optical sorter
might prove useful on a waste stream that was already presorted as glass and had been pre-
cleaned before the sorter.
Magnetic
Magnetic systems are used to separate ferrous and non-ferrous materials. In the three- magnet
system shown in Figure 8, the pickup magnet lifts ferrous material from the shredder belt;
then the transfer magnet brings the material around the curve of the belt and agitates the
material. The "no magnet" space before the discharge magnet is critical: as the material fallsfrom the belt, non-ferrous material that is caught behind the magnetic material is released.
The third magnet lifts the ferrous material back to the belt where it is discharged to the next
step in the process.
from
shredder
Solid wastes
Continuous belt
Discharge magnet
Ferrous
material
Transfer
magnetPickup
magnet
Nonferrous
materials
Typical magnetic separation system
Figure 8
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Screening
Many components in the waste stream have a characteristic size. Therefore, it is possible to
sort waste by size to achieve a series of waste streams with a higher percentage of certain
components. However, sorting by screening can never be 100% effective because of the
overlap in component sizing. Placing a screening mechanism before a shredder will reduce
loads on the shredder by removing small particles first. Various screening devices have been
developed, including vibratory screens, rotary screens and disc screens.
Vibr ator y Screens
Vibratory screens are excellent at separating relatively dry materials such as glass and metals.
A typical vibrating screen is shown in Figure 9.
Typical vibrating screen used for size separating commingled waste
Figure 9
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Mills
Mills are of several types: flail mills, vertical shaft hammer mills, and horizontal shaft
hammer mills. The vertical shaft hammer mill (Figure 13) is the most successful at achieving
size reduction, but at the cost of high maintenance and energy consumption. The steel
hammers that are pinned to the central shaft beat the waste to smaller and smaller sizes.
Shears
The shear shredder is made up of two parallel counterrotating shafts with a series of discs
mounted perpendicularly that serve as cutters. Waste material is reduced in size by the
shearing or tearing action of the cutter discs.
Small fraction
Large fraction
Schematic of a disc screenFigure 11
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200 4 8 12 16
Typical component size (in.)
10
20
30
40
50
60
70
80
90
100News-
print
Card-
board
Paper
Garbage
Yard
and
garden
waste
Metal
Glaass
Plastic
Inerts
Miscellaneous
organics
Percen
tcompos
ition
Typical size distribution of raw refuse
Figure 12
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Drive motor
Infeed
Discharge
Neck section
Ballastic
ejection
Schematic of a vertical shaft hammer mill
Figure 13
Grinding
Grinders are actually another form of the shredders that were discussed in the preceding
section. Some varieties are tub grinders and mills.
Tubs
A tub grinder resembles a large diameter wash tub on wheels. It is a variety of mobile,
hammermill shredder. The tub grinder is often used for yard wastes, pruning and construction
debris. The waste is fed into the top of the tub, and then falls into a horizontal hammermill.
The grinders are often diesel-powered and may even have their own attached crane for
loading material in the tub.
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Mills
A grinding mill operates much the same as a shredding mill but has a lower power input and
uses time and multiple passes to do the work rather than brute force.
Baling
Baling is used at recycling centers to reduce the volume of waste. This volume reduction
eases storage requirements and cuts transportation costs. Some new equipment can produce
usable commercial products (such as fireplace logs) directly from waste cardboard and paper.
Balers are an alternative to compactors and operate at 100-200 pounds per square inch
pressure to produce compact bales of solid waste or recovered materials. Bale weight is in
the range of 500 to 800 kg.
Cardboard and Paper
Since up to 50% of municipal solid waste (MSW) is paper, significant reductions in landfill
volume can be obtained through cardboard and paper recycling. Larger department stores and
grocery stores often have their own cardboard balers. The baler compresses the waste paper
and automatically bands the material together with wire to ease transport methods. A forklift
and pallet system is normally used for transport within the facility. A baler used for paper and
cardboard is shown in Figure 14.
Aluminum Cans
Aluminum is one of the easiest and cost effective materials to recycle. The cans aresometimes baled, using the same baling equipment that is used for cardboard. They can also
be crushed and blown into trailers for shipping. Single can crushers are available for home
and office use to reduce waste volume at the source.
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Baler used for paper, cardboard and cans
Figure 14
The following example problem illustrates the effectiveness of recycling in extending landfill
life.
Example Problem 1. Volume reduction by materials separation and r ecovery of
recyclables.
A community with a population of 40,000 has a per-capita solid-waste disposal rate of 7
pounds per day (as collected). The distribution of components and nominal density and
compaction factors are for a typical landfill disposal. Determine the annual landfill area
requirements without any materials recovery and with a recovery of 75% of the glass and
paper and 80% of the metals and cardboard. By what factor could such recovery extend the
useful life of the landfill?
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Solution:
Computation table. *Given or measured values.
As collected (no recovery) Collected with recovery
Component %
by wt.
*
lb.
1000 lb.
*
density,
lb./ft.3
*
volume,
ft.3 per
1000 lb.
normal
comp.
factor *
fill
volume,
ft.3
wt. for
disposal,
lb.
density,
lb./ ft.3
*
disposed
volume,
ft.3
normal
comp.
factor *
fill
volume,
ft.3
Food Waste 12 120 18 6.7 0.35 2.3 120 18 6.7 0.35 2.3
Paper 44 440 5 88.0 0.20 17.6 110 5 22.0 0.20 4.4
Cardboard 5 50 3 16.7 0.25 4.2 10 3 3.3 0.25 0.8
Plastics 4 40 4 10.0 0.15 1.5 40 4 10.0 0.15 1.5
Glass 10 100 12 8.3 0.60 5.0 25 12 2.1 0.50 1.3
Ferrous Metal 5 30 20 2.5 0.35 0.9 10 20 0.5 0.35 0.2
Tin Cans 5 50 6 8.3 0.18 1.5 10 6 1.7 0.18 0.3
Aluminum 4 40 4 10.0 0.18 1.8 8 4 2.0 0.18 0.4
Miscellaneous 11 110 10 11.0 0.25 2.8 110 10 11.0 0.25 2.8
100% 1000 lb. 161.5
ft.3
37.6
ft.3
443 lb. 59.3
ft.3
14.0
ft.3
Calculation of solid waste density:
D withoutrecovery =1000 lb.(27ft.3/ yd.3 )
37.6 ft.3=718 lb./ yd.
3
D withrecovery = 443 lb.(27ft.3/ yd.3 )
14.0ft.3
= 854.4lb./yd.3
Calculation of approximate annual landfill area without recovery:
Average weight of daily waste collected = (40,000 persons)(7 lb./day/p.) = 280,000 lb./d.
Dailyfill volumerequired=280,000lb. / d.
718lb./yd.3= 390 yd.3/ d.
Assume a landfill cell cross-section of 2 yd. depth by 8 yd. wide = 16 yd.2
Dailycell length=390yd.3
16yd.2= 24.375 yd. lengthor 73.1 ft. + .5 ft. facecover = 73.6 ft.
Daily area = (73.6 ft.)(24.0 ft. + 2.0 ft. partition wall between trenches) = 1913.6 ft.2/d.
Annual area = (1913.6 ft.2/d.)(365 d./yr.) = 698,464 ft.2/yr.
or698,464ft.2/ yr.
43,560ft.2/ac.= 16.03 acres/yr.
The change in area (fill life) with material recovery is proportional to the volume change:37.6 ft.3
14.0 ft.3= 2.69or withmaterialrecovery thelandfilllife canbeextendedby a factor
of about2.7
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Filtration
The physical treatment methods that have been discussed so far are meant primarily for
relatively dry materials. For high liquid content wastes, it is appropriate to use: filtration,
flocculation, precipitation, flotation and evaporation/drying beds. These methods are all
meant to concentrate or separate solids from the liquid wastes.
Filtration is the physical process of retardation, resulting from the clogging of pore spaces in
the filter media. This clogging occurs when solid particles are trapped in the pores. Filtration
also occurs due to precipitation and accumulation of dissolved matter. There are three
common filtration methods: filter beds, drums and presses.
Filter beds
Sand filter beds were first used in water treatment plants, but the technology has found its wayinto wastewater treatment as a final "polishing" of sewage effluent. Beds are now made of
sand, coal, dual media (sand plus coal), or mixed media (sand, coal and granite).
A filter can reduce suspended solids in wastewater from 25 mg/L to 10 mg/L. If the solids
concentration is much higher than 25 mg/L, it is better to remove the solids with treatment
such as rapid mix-flocculation-sedimentation than it is with sand. If the sand pores load up
too quickly, the drop in pressure across the filter becomes excessive. A sand filter cross
section is shown in Figure 15. As the contaminant is captured on the sand, the pressure drop
increases, and the filter must be backwashed. The waste flow to the filter is shut off, and
water is pumped upward through the filter to rinse the filter media and to wash the
contaminant to a collection point. Backwashing normally lasts only a few minutes, finally thewashwater is shut off, and the clean filter is returned to operation.
A sand filter can also be used to capture petroleum type wastes. The finer the sand and the
higher the product viscosity, the greater the product retention. Up to 20,000 parts per million
(mg/L) of No. 6 diesel oil can be retained on fine sand. The filters are up to 625 square feet
in area, and flow rates over the beds average 3 gallons per minute per square foot of bed area.
Drums
Drum, or vacuum, filters are often used to dewater sludges. A cylindrical drum is covered
with a filter fabric. The drum rotates partially submerged in a vat of conditioned sludge. Avacuum is applied to the inside of the drum through the porous filter media. This vacuum
draws the water into the drum, leaving the dewatered filter cake on the outside of the drum. A
blade scrapes the drying filter cake from the rotating drum, and the cycle starts over.
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Outlet Main
Inlet Main
Wash Water
Outlet
Graded
Filter
Sand
Perfirated LateralsGraded Gravel
Wash Troughs
Typical cross section of a rapid sand filter
Figure 15
Presses
A continuous belt filter press(CBFP) operates on the shear and compressive forces
introduced in the sludge cake when the cake is pressed between two moving belts, as shownin Figure 16.
Washwater
FiltrateWash Spray
Conditioned
Sludge
Sludge Mixer
Polyelectrolite
Solution
Chemical
Conditional
Stage
Sludge
Cake
Compression
Dewatering
Stage
Gravity
Drainage
Stage
Continuous belt filter press
Figure 16
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Flocculation
Heavy metals removal from wastewater can be greatly increased by the addition of various
water-soluble chemicals and polymers in the dual process of coagulation and flocculation.
The two processes are used when normal settling rates of suspended particles are too slow for
effective clarification.
Coagulation is the addition and rapid mixing of a coagulant to neutralize charges and to
collapse the colloidal particles . This chemical addition and mixing causes agglomeration and
settling of the particles. Rapid mixing destroys the stability of the colloidal system. For
agglomeration to occur, the particles must collide; mixing helps that occur. Rapid mix times
of 30 seconds to 5 minutes are typical for the 8 cubic meter (maximum size) mixing basins.
Flocculation is the agglomeration of colloidal particles that have received coagulant
treatment. Flocculation takes place under slower mixing conditions in a 30-minute detentiontime tank.
Common coagulants are alum and iron salts for surface waters, and lime-soda mixes to soften
"hard" groundwater. Organic polymers, called polyelectrolytes, are often more effective than
these natural materials, at least for surface water treatment. There is no substitute for
laboratory jar testing to find the best combination of treatments for a particular water or waste
stream. Coagulants can also be added to wastewater settling tanks to promote better removal
of suspended solids.
The floc settles out in a sedimentation basin. The basin is sized for a 2 to 4 hour detention
time; again, this detention time depends on the treated material.
The agglomerated, flocculated waste must be handled properly for disposal. If the process is
designed to remove heavy metals, the waste will likely be classified as hazardous. Water and
most wastewater sludges can be recycled. The high calcium content in hard water sludge
makes it useful for concrete and gypsum additives.
Precipitation
Heavy metals are often present in liquid waste streams. Metals will precipitate at different pH
levels; this precipitation results in an insoluble salt that can be removed as a sludge. Lead,
for example, is soluble at acid pH, so lead in pipes is more of a problem at low pH. When anacid waste stream containing heavy metals (such as lead) is neutralized, the metals can be
removed by clarification, sedimentation, or filtration.
Lime is commonly used as a precipitate; sodium sulfide and sodium bisulfide can also be
used, but they present some danger of hydrogen sulfide release during the precipitation
process.
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Flotation
Flotation works well for low-density solids and hydrocarbon solids that can be separated from
liquids by air injection. Finely divided bubbles of air are injected into the liquid and attach to
the particles to be "floated." The particles, with their air "life preservers," rise to the water
surface and can be mechanically skimmed. Several mechanisms account for the air bubble
effectiveness, including actual bubble attachment to the particles, bubble formation at the
solid-liquid interface, and air entrapment in larger particles or air integration into the floc
itself. Care must be taken to avoid corrosion with air injection. The biology of the well and
the use of biocides are factors in flotation effectiveness.
Evaporation
Evaporation has been used for centuries to separate materials. Our ancestors evaporated salt
water in large pans to recover the valuable salt for trade. The technology changed little overthe years. Evaporation is defined as a treatment method by which wastewater is dispersed in a
vaporous form.
Ponds
The SAES-A-104, Wastewater Reuse and Land Disposal Engineering Standard addresses two
types of evaporation ponds: percolation/evaporation ponds and wastewater evaporation
ponds.
Percolation is a disposal method by which wastewater is allowed to pass through the soil base
of the pond. A percolation pond for wastewater requires the approval of the Chief Engineer,with the concurrence from the General Manager, Exploration; Chief, Preventive Medicine
Services; and Chief, Environmental Affairs. Percolation should not be used if the wastewater
contains hazardous waste, because of the potential danger of groundwater contamination.
If a pond is to be used for evaporation of wastewater, the SAES-A-104 Standard requires the
wastewater to be of "at least primary effluent quality," and the pond to be lined to prevent
percolation. Primary effluent is defined as the effluent from a process that provides removal
of sewage solids so that the effluent contains not more than 500mg/L of suspended solids.
The pond liner may be naturally occurring or man-made, and the coefficient of permeability
for the liner system must be less than or equal to 1 x 10-8 cm/sec. Wind velocity has a strong
effect on pond evaporation rates.
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Drying Beds
Drying beds have been used for decades at wastewater treatment plants. The purpose of the
beds is to dewater digested sewage sludge economically. The sludge is removed from the
beds after drying. The sludge is then disposed of in a landfill or used as a soil conditioner in
some countries. Saudi Aramco regulations prohibit sludge use for fertilizer. Drying beds are
low cost and low maintenance, and provide a high solids content in the dried product. Nature
does the drying work, rather than vacuum or horsepower. Four types of beds are used:
conventional sand, paved, artificial media, and vacuum-assisted.
A conventional sand bed is shown in Figure 17. Sand beds are useful for cities up to 20,000
persons. Larger cities should consider alternate methods because of the large space
requirements for sand beds. Typical area requirements are shown in Table 1.
Table 1. Typical area requirements for open sludge drying beds.
Type of sludge
Area,
ft2/per son
a
Sludge-loading r ate,
lb dr y solids/ft2.yr
Primary digested
Primary and trickling-filter humus digested
Primary and waste activated digested
Primary and chemically precipitated digested
1.0-1.5
1.25-1.75
1.75-2.5
2.0-2.5
25-30
18-25
12-20
20-33aCorresponding area requirements for covered beds vary from about 70 to 75 percent of those for the openbeds.
Note: ft2
x 0.0929 = m2
lb/ft2
x 4.8828 = kg/m2
. yr
Two types of paved drying beds are in use: a drainage type and a decanting type. The former
type is similar in size or larger than a conventional sand bed. Drying is encouraged by
frequent agitation with mobile equipment, and the dried sludge is removed with front end
loaders. There is generally less maintenance because there is no sand to be replaced
periodically. The decanting bed is shown in Figure 18. The slope of the bed allows
supernatant to be drawn off at the bed corners. The drying sludge is also mixed, similarly to
the drainage type bed. The decanting design works well for arid, or semi-arid areas. The
design requires evaporation and precipitation rates, plus pilot studies, to determine the
effectiveness for a particular sludge.
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Artificial media beds have been developed to overcome some of the cost and space
disadvantages of the sand and paved beds. Stainless steel wire mesh and polyurethane mesh
are used with some success. The polyurethane system works well for dilute sludges, and the
system produces a filtrate with low suspended solids.
Vacuum drying beds use vacuum on the underside of a stationary, porous, media plate to
assist gravity sludge dewatering. Dewatering proceeds over a 2-day period, which is much
shorter than with conventional sand filters. Filter size advantages are balanced by the need
for further post processing to obtain additional moisture reduction.
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METHODS OF CHEMICAL TREATMENT OF SOLID WASTE
Chemical treatment of municipal solid waste usually involves a form of chemical conversion
of the waste to a product, following some pre-processing. Chemical treatment is helpful in
promoting resource recovery of hazardous substances. Chemical treatment can also produce
useful by-products and residual effluents that are environmentally acceptable, which makes
chemical treatment a better method of waste management than the traditional landfill or
incinerator. Several processes are in common use:
Acid hydrolysis
Alkaline hydrolysis
Oxidation
Reduction
Neutralization
Calcination
Ion exchange
Other methods, such as dehydrohalogenation
As was discussed briefly in Module ENV 102.01, hydrolysis processes may be used torecover compounds such as glucose and furfural. The chemical process known as hydrolysis
occurs when chemical substances react with waste molecules. For example, acid hydrolysis
can convert cellulose into glucose. A cellulose molecule (consisting of about 3000 glucose
units) is soluble in water and in many organic solvents and is poorly degradable by
microorganisms. However, when the cellulose molecule is acid hydrolyzed, glucose and
other sugars may be recovered. The process involves treating a suspension of small cellulose
particles with a weak acid, heating the particles to between 180 and 230 C under pressure (to
prevent boiling and to allow for achieving those high temperatures). The quantity of glucose
that is recovered will depend on the characteristics of the waste and the process efficiency.
With good process efficiency, for example, and with kraft paper as the cellulose source,
approximately 80% of the weight of the kraft paper may be recovered as sugar. Therecovered sugars may be converted by biological processes and other chemical processes into
alcohols and other industrial chemicals. The general acid hydrolysis reaction for cellulose to
glucose is:
(C6H
10O
5)n + H
2O acid nC
6H
12O
6
cellulose glu cose
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Oxidation
Chemical reduction-oxidation (redox) reactions can take place with both organic and
inorganic chemicals. A redox reaction traditionally involves the gain or loss of oxygen. An
oxidation reaction adds oxygen to a compound. An example of an oxidation reaction is
FeSO4 changing to Fe2 (SO4)3. However, it is possible to have a redox reaction without
oxygen. With organic chemicals, oxidation is defined as the loss of electrons by a chemical (
the chemical donating the electron is oxidized). For inorganic materials, oxidation is better
defined as a reaction that raises the oxidation state of an atom. In the previous example, iron
(Fe) went from a +2 valence to +3, so it was oxidized.
Redox reactions in solid waste are mostly the result of biological activity, but some chemical
redox reactions can occur between organic materials and the soil. Some researchers have
found the oxidation of aromatic chemicals at soil and clay surfaces, catalyzed by adsorbed
oxygen and trace metals. These reactions can particularly occur in aerated unsaturated soil.Chlorinated organics do not seem to undergo such oxidation. Thus, one would expect that it
is easier to degrade aromatics than chlorinated solvents under natural aerobic conditions in
clay soils.
A common method of treating aqueous cyanide wastes is alkaline chlorination. The cyanide
is initially oxidized to a less dangerous cyanate form and then to carbon dioxide and nitrogen
in the following pair of reactions:
a +2
+ a a + a +2
2NaCNO + 3Cl2 + 4NaOH 2CO2 +N2 + 6NaCl+ 2H2O
This reaction is pH sensitive: The first reaction must be above pH = 10 for the cyanate to be
formed. The second reaction works better at pH = 8. Since hydrogen cyanide gas can be
released at acid pHs, one must really watch this reaction! The process can utilize
hypochlorite bleach, peroxide or ozone, so the process is useful for cleaning up spills of
cyanide or for disposing of cyanide wastes in a treatment method.
Another practical oxidation process for waste destruction is the Zimmerman wet air oxidation
method. Most organic compounds can be air-oxidized, if there is sufficient temperature and
pressure present. This process is an aqueous phase oxidation of dissolved and suspended
organics at 175 to 325 degrees Centigrade with enough pressure to prevent excessiveevaporation. With air bubbled through the liquid, the process is fuel efficient and usually
self-sustaining. Even some pesticides can be destroyed by this method.
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Reduction
A reduction reaction is a reaction that involves a decrease in valence from a gain of electrons.
A reduction-type reaction can be useful for the disposal of hexavalent chrome, a highly toxic
waste that is dangerous to both man and the environment. The hexavalent chrome can be
reduced to the much less toxic trivalent chrome by reacting the hexavalent form with sulfur
dioxide and lime. Reduction can also be used with most other metals to create an easily
removed precipitate. Redox treatment methods can, in general, be used for both in-situ and
ex-situ waste disposal procedures.
Neutralization
Many wastes, especially liquids, sludges and slurries, may be highly acidic or alkaline. The
best first step in treatment is to bring the waste to almost neutral pH. This neutralization
process will ease handling and improve the effectiveness of follow-on treatments.Neutralization effectiveness is easily measured by pH change, and acid-base reactions are
among the most often used processes in wastewater treatment. Several methods of
neutralization are practical:
Mixing multiple waste streams to achieve a neutral pH
Adding lime slurries to acidic wastes
Adding caustic soda or soda ash to acidic wastes
Adding carbon dioxide to alkaline waste
Adding sulfuric acid to alkaline wastes
All of these methods are effective, but it should be noted that, under RCRA regulations, such
operations cause a facility to be regulated as a treatment-storage-disposal (TSD) operation.
Even where RCRA does not apply, indiscriminate neutralization can be dangerous. The
reactions can give off considerable heat (exothermic reactions). In the case of cyanide at high
pH, overly enthusiastic neutralization could cause cyanide gas release, if the pH were to
become acidic during neutralization.
Materials can be neutralized in a simple reaction vessel as shown in Figure 19. Occasionally,sludges are treated in situ by mixing soda ash or lime with the sludge in a pond or lagoon.
Neutralization on a small scale is also useful for disposing of laboratory chemicals.
Since stack flue gases often have a high carbon dioxide content, such gases can be used to
neutralize alkaline wastes.
Good practice calls for bringing the waste to a near neutral pH (6 to 8), rather than to simply a
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RCRA non-hazardous waste condition (2 < pH < 12.5) .
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MIXER
pHmeter
Neutralizedeffluent
Neutralizer
Wastestream
Chemical neutralization treatment system for waste management
Figure 19
Calcination
The recovery of the large amount of calcium that is needed for the softening of hard waters iseconomically attractive. To be used again, the dried, calcined, dewatered sludge must not
contain much magnesium. Calcination is the process of heating dried solids to drive off
carbon dioxide. Both calcium oxide (CaO) and Magnesium Oxide (MgO) are produced by
the calcining process. Incidentally, the carbon dioxide driven off in the calcining may be used
for carbonation of the softened water.
Ion Exchange
An ion exchange system selectively exchanges ions from a chosen material in the waste
stream for the exchange medium. Two types of exchange systems are available: cationexchangers and anion exchangers. Cation exchangers are employed to remove positively
charged materials (metals), and anion exchange units are used to remove negatively charged
materials, such as organics. The primary use for ion exchange has been to remove metals
from ground waters and surface waters. Metals are concentrated in the resin column and can
then be removed by backflushing with water. The resin bed is then recharged by passing
dilute acid through the bed. It is possible to achieve removal efficiencies of better than 99 %,
with an effluent quality of less than 100 ppm of metal.
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Most water hardness is due to the presence of calcium and magnesium hardness. The water
can be softened by passing the water through an ion exchange resin. Generally, the ion that is
exchanged with the hardness is sodium, as indicated in the following equation:
Ca(HC3 )2 + 2NaR CaR2 + 2NaHCO3
where R is the ion exchange material. With this reaction, calcium or magnesium has been
removed from the water and replaced by an equivalent amount of sodium. This process
removes almost 100 % of the water hardness until the exchange capacity of the resin is
reached. At this point, "breakthrough" has taken place. The resin is taken off line and
backwashed with water containing a high sodium content. The hardness on the resin will
enter the backwash water as follows:
CaR2+
2NaCl
2NaR+
CaCl2
The resin bed is now ready to remove additional hardness; however, the CaCl 2 must be
disposed of, or a recycle use for it must be developed.
Ion exchange can also occur naturally in soil, particularly clay soils. The capability of a soil
to retain and exchange cations is called the cation exchange capacity. Clays have a higher
cation exchange capacity than other inorganic particles because clays have a large surface
area, with numerous charge sites.
It is important to note that ion exchange of metallic ions with soil may be partially reversible:
exchange sites which are saturated can release cations as concentrations of contaminantsdecrease in groundwater. This means that, as groundwater contamination is remediated, more
and more contamination that was bound up in a clay soil can be released: consequently, the
clean-up effort will take far longer than expected. The exchange sites can also release cations
if the pH is lowered. Ion exchange in the natural environment is, therefore, more of a
retardation, than an attenuation process. In addition, the exchange capacity of the subsurface
material can be so saturated that the contaminant transfer is not affected by ion exchange, and
contaminant transfer goes unretarded.
Other Chemical Methods
The safe treatment of PCBs and dioxins is a major concern when handling solid waste. Adechlorinization process was developed as an alternative to incineration of chlorinated
compounds. The underlying principle of dechlorinization is the removal of the chlorine atoms
from the compounds. The dechlorinization process employs synthesized reagents to break
down the chlorinated molecules or to form other compounds that are less toxic to the
environment and man.
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The most often used dechlorinization processes use polyethylene glycols (PEG) that have
reacted with alkali metals to bring about the dechlorinization. The two most common
processes are called the Alkali Polyethylene Glycol Process (APEG) and the Potassium
Polyethylene Glycol Process (KPEG). Either process will work in the field or the traditional
plant. Removal efficiencies of 99.5 % have been demonstrated. This efficiency, although
certainly desirable, is well below the efficiency of the best incinerators.
Three factors must be considered for any chlorine destruction process:
Temperature of the material
Contact time between the contaminant and the reagent
Moisture content of the soil
Elevating the waste temperatures from 20 to 80 Centigrade increases the reaction efficiency
from 50 % to 90 %. Contact time varies from 4 to 8 hours for ex-situ work, up to an average
of 7 days for in-situ treatment. Water adversely affects the reaction; soil moisture is,
therefore, a factor in the extended contact time required for in-situ treatment. Both APEG and
KPEG appear to have equal effectiveness. At this point in time, the major concern with
dechlorinization is that the reaction byproducts have not yet been well defined. Since U.S.
EPA has stated that dioxin is one of the most toxic substances known, it is well to proceed
with caution when attempting to destroy the material.
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LANDFARMING AND COMPOSTING AS SOLID WASTE TREATMENT
METHODS
Landfarming and composting are so similar in concept and requirements that the two
processes will be discussed together.
A landfarm is a biological treatment method that employs soil and associated microorganisms
as the treatment medium. The natural physical, chemical, and biological actions all come
together to degrade and immobilize the waste constituents. Some types of waste are not
actually degraded, and are incorporated only into the soil. When that occurs, landfarming
becomes a shallow, unlined landfill and is, therefore, a method of disposal, not treatment.
Composting is the process of making a nonputrescible (non-rotting) soil amendment from
solid waste. Many components of municipal solid waste are organic in origin and are
therefore biodegradable. Paper, yard waste, food waste and some textiles, such as cotton andwool, can all be composted. Composting of waste will occur readily, if there are present
appropriate microorganisms, adequate aeration, temperature in the correct range, required
nutrients, pH and sufficient moisture.
Landfarming has been used for:
Oily sludges and waste oils, such as separator sludge, slop oil emulsion solids,
induced and dissolved air flotation float, and leaded and unleaded tank
bottoms. Half-lives of the materials are typically 200 to 500 days. Oil loading
rate is usually the governing factor, although heavy metals in wastes such as
tank bottoms are sometimes limiting.
Organic sludges and liquids. Any waste that can be degraded biologically can
be landfarmed if regulations permit it. Halogenated sludges must be handled
very carefully to avoid problems during the sludges' slow decay time.
Sludges from wastewater treatment plants. Heavy industrial activity in a
community can cause high metals content in sewage sludge. Sludges are
monitored periodically to ensure the waste stays within the plant's operating
permit.
Careful attention must be made regarding the composition of the waste when considering aland disposal option. The US EPA has ranked all hazardous wastes based on their intrinsic
hazard, volume, and phased land disposal. "Land ban" restrictions were enacted in three steps
with the final enactment in May 1990. In order for land disposal (and also impoundment or
deep well injection) to receive approval, listed hazardous wastes must be pretreated to
pollutant concentrations below specified concentrations. It must also be demonstrated, to a
reasonable degree of certainty, that there will be no migration of hazardous constituents from
the disposal site.
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Saudi Aramco has established guidelines (Refinery Instruction Manual 5.881) for landfarming
wastes as follows:
1. Landfarmable wastes:
API separator sludges (less than 20 ppm organic lead)
Air flotation sludges
Biological waste treatment sludges
Recovered oil emulsions
Tank bottoms (excluding gasoline tanks)
Crude tank bottoms
MEA sludge
Oil contaminated soil (less than 20 ppm lead)
Desalter bottoms
Perhaps even more important than the list of what can be landfarmed, is the list of what the
Instruction Manual says can not be accepted for landfarming:
2. Wastes not acceptable for landfarming:
TEL tank bottoms
Leaded gasoline tank bottoms
Sweetening process sludges
Sludge from sulfuric acid treating
Caustic sludges
Spent acid
Catalyst from conversion processes
Asphalt waste
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Bacteria also are categorized by their atmospheric oxygen requirements as aerobic (require
atmospheric oxygen) anaerobic (require a lack of atmospheric oxygen) or facultative
anaerobic (function with or without oxygen). This environmental need will determine the
type of bacteria that are available to function in the treatment process. The oxygen
requirement also determines the rate at which treatment will progress and the resulting end
products, which differ with aerobic or anaerobic biological activity. For example, methane
will be a product of anaerobic activity but not of aerobic action. Most of the bacteria types
listed for petroleum product degradation are classified as aerobic bacteria.
Other critical environmental factors are temperature, pH, and moisture content. Optimal
biological activity occurs within a fairly narrow range of temperature and pH for specific
groups of bacteria although some activity can occur at less than an optimum rate outside the
preferred range of temperature and pH.
Generally, a warm environment (20-50 C) encourages biological activity. The optimum for
many bacteria is 35 C, although higher temperatures (about 55 C) may be optimal for some
bacteria. Fortunately, the bacteria most effective for petroleum products prefer temperatures
between 35 C and 45 C. The higher temperatures are also desired for the destruction of
pathogenic (disease-causing) microorganisms.
A near neutral pH range of about 6.5 to 7.5 is best for most bacteria. Soil pH of less than 5.5
is considered unacceptable.
Several other soil and site characteristics will determine the suitability of an area for
landfarming:
Soil depth must be greater than 2 feet.
Restrictive subsoils must be greater than 8 feet from the surface.
Highly permeable soil, such as sand, gravel, rocks and stone are undesirable.
High salinity or alkalinity can interfere with biological processes.
High background levels of certain metals or organics can make it difficult to
determine how "clean" the site is.
A water table closer to the surface than 8 feet (in sandy soil) or 6 feet (in loamy
sand) is unacceptable due to probability of off-site pollution migration.
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Moisture is critical to bacterial and other microbiological activity since about 80% of the cell
weight is water and since the nutrients for bacteria must be in solution to pass into the cell.
Supplemental water may be required for landfarming or composting municipal solid waste.
On a weight basis, the favorable moisture content for landfarming varies from 10-30%,
depending on the soil texture. This is equivalent to 50-70% of the soil water holding capacity.
It is important not to totally saturate the soil, or the bacteria will "drown," and the process will
become anaerobic. The desirable moisture content for composting is usually in the 50%
range. In non-arid climates with mild temperatures, these moisture contents can be achieved
with two inches per month of rainfall or applied water. With Saudi Arabia's summer
temperatures and minimal rainfall, considerable monitoring and adjustment will be needed to
reach these moisture contents.
In landfarming, wastes are applied uniformly to the land, either by spreading the wastes or by
injecting the wastes just beneath the surface. A disk harrow or rototiller (for small scale
operations) is used to mix the waste and soil. Cultivation maximizes the soil-waste contact.Furthermore, cultivation provides aeration to enhance the biological process. The cultivation
takes place in only the first 10 to 30 cm of soil depth (called the "zone of incorporation"), but
the "soil treatment zone" appears to extend to as much as 1.5 meters. Thus, landfarming is
primarily a shallow depth, aerobic process. It is common to till the soil at three week intervals
for at least the first three months of degradation.
Landfarming works best primarily with organic wastes, but landfarming can also remove
other contaminants. Suspended solids are removed by filtration on the soil and by physical
settling. Heavy metals can be adsorbed onto soil particles. Heavy metals also can be
precipitated or can undergo ion exchange with the soil. Some soils , particularly clays, have
a high sorption capacity for metals. Still, metals are often somewhat problematic. Tostabilize a heavy metal waste usually requires an alkaline pH. Such a high pH may not be
optimum for bacterial action. Metals may not be actually toxic to the microorganisms in the
soil. However, a high metals concentration may affect later plant growth when the site is
closed. Plant uptake can also act as a removal mechanism. Finally, the waste can simply
volatilize, or can be blown from the site on airborne dust. Thus, a heavy metal, such as lead,
can actually be transported from the site.
Both sandy and clay type soils have worked well for landfarms. Organic loadings as high as
5 to 10% of the soil volume (first 10 to 30 cm) are practical. Wastes are sometimes covered
in cold climates. Covering the waste raises the temperature and encourages bacterial growth.
Loading rates of 250 tons per acre per year are typical for petroleum wastes and are limited to300 dry tons per year per acre by SAES - A-104.
For landfarming to be successful, the rate and frequency of waste application must not exceed
the assimilative capacity of the site. This assimilative capacity is based on:
Capacity limits. Conservative, immobile wastes accumulate in the soil and
eventually reach a level at which the site must be closed.
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Rate limits. Non-conservative waste constituents will degrade, but the
cumulative amount applied must be compared with the cumulative amount
degraded over time. Refinery Operating Instruction 5.883 allows the
reapplication of sludge when the oil and grease content in a section of the
landfarm is lowered to 2% or less for two successive samplings.
Application limits. If the application rate is too high, waste can leave the site in
water runoff or waste can volatilize excessively.
Mathematical models are available to evaluate these various limits. A simple first order
reaction equation is often applied to determine the time required to degrade a waste to a final
soil concentration as follows:
t = ln(Ct/C0)/-K
where:
t = time to degrade
C0 = initial soil concentration
Ct = final soil concentration
K = first order rate constant
Removal efficiencies for common wastes can be remarkably high with landfarming:
In a Canadian study, a waste with 15,000 micrograms/gram each of benzene
and toluene was reduced to the required limits in soil of 5 and 30micrograms/gram for the two compounds, respectively, in less than 11 days.
Benzo(a)pyrene in the same waste took 294 days to degrade. Finally, arsenic, a
heavy metal that does not degrade, caused the abandonment of the site after
four years when the toxic limit (50 micrograms/gram) for arsenic was reached.
In a California laboratory experiment using soil contaminated with weathered
crude, the contamination was reduced from 3700 ppm to 1000 ppm in just 80
days. This experiment involved daily water addition, oxygenation and nutrient
addition. A "control" sample, which was untreated, went from 3700 to 3500
ppm in the same period. In a follow-up field pilot study, nutrient and surfactant
addition were required to get readings below 1000 ppm - water and aerationalone would not do it. The 1000 ppm standard is a common site clean-up limit
used by regulatory agencies in the United States.
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As stated previously, composting is used to turn MSW into a usable, useful product. Most
composting operations begin with the removal of the approximately 10% non-degradable
fraction, prior to starting the composting process. Glass, metal and plastic that do not
compost are all potentially valuable to sort and recycle. Removal of hazardous waste is
particularly important, although very difficult to achieve in practice. The wastes to be
composted are then shredded. The shredded materials are then placed in "windrows" on the
ground surface where the composting takes place. The primary difference between
composting and landfarming is that composting takes place on the ground, while landfarming
takes place in the ground. Composting, like landfarming is an aerobic process which requires
moisture control (40-65%, with 50% being optimal), temperature (55 C, or 131 F) for three
consecutive days to kill pathogens) and thorough oxygenation. The very high temperatures
are achieved even in winter due to the biological activity of the waste. The oxygenation can
be obtained by either of two methods: agitated piles, or static piles.
In the agitated method, the piles are 6-10 feet high and 14-25 feet at the bottom. Equipmentsuch as a Willibald side slicer is used to shave off a portion of the pile, moving it laterally
and aerating it at the same time. A "straddling turner" can also be used to aerate the pile in
place.
In the static method air is pulled or passed through the pile with an air blowing system.
Pulling the air through the pile by a system of surface grates or piping has the advantage of
allowing treatment of the exit air for odors. Blowing air through the pile allows the addition
of moisture or heat to the pile to control temperature and soil humidity.
Besides time, temperature and turbulence, the ratio of carbon-to-nitrogen has been found to be
rather critical in composting. The desirable C:N ratio is 20-30:1, with 30:1 often consideredas an optimum. Low C:N ratios can result in ammonia off gassing - a highly irritating odor.
High C:N ratios will eventually have a lower growth rate as the nitrogen is used up in the
process.
The whole composting process can take from 2 weeks to 18 months, depending on the degree
of process control. A 2.5 acre facility can handle approximately 50 tons per day of compost
(assuming a 2 month holding time), while each additional acre gains an additional 50 tons per
day capacity.
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THERMAL DESTRUCTION MET HODS OF SOLID WASTE TREATMENT
Great progress has been made in thermal destruction methods compared to the open burning
of trash that was practiced until recent times. Open burning of waste is still a factor in some
less populated rural areas. However, the pressure of urban and population growth has
virtually eliminated open trash burning in major population centers. In New York City, for
example, until the 1970s almost every multi-family housing unit (apartment house) had a
single chamber incinerator that was only a little improvement over open burning. Single
chamber incinerators were banned in New York in the 1970s, and replaced by trash
compactors at each apartment house. Open burning gives little volume reduction, compared
with more effective incineration methods, and sufficient organic residue remained in the
partially burned waste to still attract vermin and cause odors.
There is still a place in smaller communities for the open burning of yard clippings (grass and
small branches), but even a relatively small community should consider composting thesewastes for a mulch or fertilizer.
Thermal processes have lost some popularity recently as the method of choice for hazardous
waste destruction. The threat of incomplete waste combustion, even if the threat is
unfounded, has caused the U.S. public to oppose new incinerator locations. Three types of
thermal destruction methods will be discussed in greater detail: incinerators, pyrolysis, and
the "emerging technologies" of microwaving and plasma arc. Except for vitrification, which
will be discussed in the next section, thermal technologies are ex situ processes: the waste
must be transported to the processing unit.
Incineration
Thermal treatment, to most people, means the incineration of waste. Incineration can be
defined as the burning of substances by controlled flame in an enclosed area. The desirable
features of incineration are that incineration:
Detoxifies hazardous waste by destroying organic compounds
Reduces the volume of the waste
Converts liquid wastes to solids by vaporizing any fluids present in the waste
Sterilizes medical wastes
Recovers waste heat from high heat content wastes
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Incineration can be designed to treat waste in any physical state-solids, liquids, sludges,
slurries and gases. Incineration has been especially successful at destroying organic matter in
waste. Removal efficiencies as high as 99.9999 % have been reached. Air emission
regulators refer to such efficiencies as "six-9s" treatment level.
Incinerator effectiveness depends on three factors, which are often cited as the three "T"s of
combustion:
Temperature of the combustion chamber
Time -- the residence time of the waste in the chamber
Turbulence -- the amount of mixing of the material with air while in the
chamber.
In addition, oxygen (from the air), if present in excess, will drive the combustion reactions to
completion more quickly. If a stoichiometric quantity of oxygen is all that is available, the
reaction will still eventually go to completion. However, excess air will greatly increase the
rate at which combustion is achieved. Different materials also have different excess air
requirements. Air that is sufficient to burn natural gas cleanly, for example, is insufficient for
a heavy fuel oil. Black smoke would result from the incomplete fuel oil burn. Even propane
and natural gas (methane) have different air fuel requirements; a burner that is sized for
propane will produce excess carbon monoxide if it is used with natural gas. Normal
combustion temperatures vary between 900 1500 Centigrade, and occasionally much higher
temperatures are experienced. One of the major difficulties with burning unsorted municipal
waste is the tremendous range in heat content of the waste. Raw, wet garbage requires agreat deal of supplemental fuel to burn; plastics, in contrast, have so much heat content that
they can heat damage the incinerator walls.
Most modern incinerators employ two combustion chambers. The first chamber's function is
to convert the compound to a gas and initiate the combustion process. The second chamber
completes the combustion of the gases. Auxiliary fuel to maintain combustion is normally
added in the primary (first) chamber and sometimes in the secondary chamber. A two-
chamber incinerator is shown in Figure 20. The grate where the waste material is placed in
this incinerator is fixed in position. Such an incinerator can support a grate loading of about
30 lb/hr-ft2. If the as-received heating value of the waste is 4000 to 5000 Btu/lb, then the heat
release rate from the grate will be 120,000 to 150,000 Btu/hr-ft2. Although the fixed gratemight prove satisfactory for a small apartment house incinerator, most larger incinerators
employ a so-called "spreader stoker" to spread the waste on the grate and to ease ash removal.
Several varieties of spreader stokers are shown in Figure 21.
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Curtainwall port
Mixing
chamber
Cleanout doorsunderfire air ports
Fixed
grates
Primary combustionchamber
Secondarycombustion
chamber
Curtain
wall
Secondaryair port
Flame portCharging doorwith overfire
air ports
Cutaway of an in-line multi-chamber incinerator
Figure 20
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(a) Stationary
(c) Oscillating (d) Traveling
(b) Dumping
Types of grates available for combustion of solid fuels
Figure 21
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The spreader stokers in Figure 21 throw the fuel mechanically across the grate from the fuel
hopper in the right-hand side of the drawings. The grates in Figure 21 (a) are still fixed in
place. This fixed grate system requires the ash to fall through the grate without any grate
movement. Airholes in the grate for the underfire air can be blocked by the refuse, which
affects combustion efficiency. In Figure 21 (b), the grates can be rotated mechanically to
dump ash into the bottom ash pit. The air holes can be smaller in size; the smaller air holes
lessen the chance of unburned waste dropping into the ash pit. Two types of oscillating or
travelling grates are shown in Figure 21 (c) and (d). This style of grate lessens the blockage
of air holes and generally improves combustion. Heat release rates for a spreader stoker can
approach a million Btu/hr-ft2, which is six to eight times that of a stationary grate incinerator.
All of these systems, except for the stationary grate, could be considered for use in refuse-
derived fuel (RDF) combustion because of the uniformity of the fuel. Unprocessed fuel is so
variable that a different type of grate has proved to work better. Figure 22 illustrates a stair-
step grate arrangement, with every other step being held stationary. The moveable steps areslowly moved back and forth, pushing the refuse towards the ash hopper. As the refuse falls
from one step to the next, its surface area is exposed for a longer and longer time. It is
essential to provide this mixing or turbulence capability when working with unprocessed
refuse.
In Figure 23, a mass-fired municipal combustor is repeated here from Module ENV 102.01.
This incinerator is used for the large-scale conversion of municipal solid waste , with energy
recovery to electrical energy as used in Los Angeles, California. The detailed steps of the
process are given after the figure.
By using a conversion from megawatts (million watts ) to Btu/hr, one can estimate the amountof energy produced by municipal refuse. If the overall combustion-to-energy conversion
efficiency is 33% (typical), then one must put in 3 megawatts to get 1 megawatt output:
3 megawatts x 3.413 x 106 Btu/hr/megawatt = 1.02 x 107 Btu/hr
if refuse = 6000 Btu/lb, then
1.02 x 107 Btu/hr 6000 Btu/lb = 1700 lb/hr per megawatt out
Thus, almost a ton of refuse per hour is required to generate a megawatt of electricity.
Although this sounds like a great deal of refuse, a city of 25,000 persons producing 5lb/person/day of refuse will equate to 2.6 tons per hour of waste. The generation of 3
megawatts of electricity from this amount of waste should be compared very carefully to the
option of landfilling the waste.
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Mechanically fired incinerator with reciprocating grates
Figure 22
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Section through a typical continuous-feed mass-fired municipal combustor that is used for
energy production from municipal solid waste. (courtesy of County Sanitation Districts of
Los Angeles County, California)
Figure 23
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The operations of the process in Figure 23 are:
1. Solid wastes are received from the collection trucks.
2. Wastes are temporarily held in a storage pit (about 2 days waste volume
capacity).
3. An overhead crane transfers the waste from storage to the charging chute.
4. The charging chute conveys wastes to the furnace chamber.
5. The waste is burned in the furnace chamber.
6. The grates retain wastes while they are burned.
7. The combustion chamber burns gases and small organic particles that rise due
to a forced air draft. Temperatures are generally in excess of 1600 F.
8. The boiler recovers heat from the hot gases using water-filled tubes for the
production of steam.
9. The steam is used to drive a turbine-generator to produce electricity.
10. Ammonia injection is used to control the NOx (nitrogen oxides).
11. A dry scrubber is used to control the SO2 (sulfur dioxide and acid gas controlby neutralization with lime).
12. A fabric filter (bag house) system is used to collect particulates.
13. A fan is used for inducing a draft to help overcome head loss through the air
pollution-control equipment and to supply air to the combustion process.
14. Cleaned gases are discharged through a high stack for atmospheric dispersion.
15. Ash and unburned residue from the grates fall to a hopper where they are
quenched with water.
16. Furnace ash and fly ash from the dry scrubber and bag house are conveyed to
ash treatment and disposal facilities. Ash should be tested against hazardous
waste disposal criteria.
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In the preceding Figure 23, a baghouse was used for particulate control. Baghouses will
likely work better than electrostatic precipitators (ESP) for applications in mass burn
incinerators because of the variability of the fuel input. ESP's are very sensitive to a particle
property called resistivity. The ESP efficiency will vary as the fuel feed resistivity varies,
and the fuel feed naturally will vary greatly with municipal waste.
Solid wastes principally contain these elements: carbon, hydrogen, oxygen, nitrogen, and
sulfur. Lesser quantities of other elements (various metals, for example) may be found in the
ash residue. When the waste is burned with the addition of stoichiometric quantities of
oxygen (or air) that is needed for complete combustion, the typical gaseous products are
carbon dioxide (CO2), water (H2O, flue gas), nitrogen (N2) and small amounts of sulfur
dioxide (SO2). The reactions for the oxidation or combustion of C, H, and S (and their
atomic weights) as contained in municipal solid waste are as follows:
for carbon: C+
O2
CO212 32
for hydrogen: 2H2 + O2 2H2O
4 32
for sulfur: S + O2 SO232.1 32
The stoichiometric amount of air that is required for each of the above combustion reactions
may be calculated as follows:
If it is assumed that dry air contains 23.15% oxygen by weight, the amount of air
required for the oxidation of 1 pound of carbon, hydrogen and sulfur, respectively, will
be:
(32/12) (1/0.2315) = 11.52 lb. air/lb. carbon
(32/4) (1/0.2315) = 34.56 air/lb. hydrogen
(32/32.1) (1/0.2315) = 4.31 lb. air/lb. sulfur
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An example of the calculation for determining the amount of air required for the combustion
of an organic solid waste follows. Note that in step 2 of the Problem, the %'s are given in %
by volume; in step 3 - 5, the %'s are by weight.
Example Problem 2. Determ ination of the stoichiometr ic amount of air r equired for the
combustion of an organic solid waste.
Determine the amount (lbs and ft3) of air that is required for the complete combustion of one
ton of an organic solid waste. Assume that the composition of the organic waste to be
combusted is given by C5H12. Assume the specific weight of air is 0.075 lb/ft3
Solution:
1. Write a balanced stoichiometric equation for the oxidation of the organic compoundbased on oxygen:
C5H
12 + 8O2 5CO2 + 6H2O
72 256
2. Write a balanced equation for the oxidation of the organic compound with air. In
combustion calculations, dry air is assumed to be comprised of 21% oxygen and 79%
nitrogen. Thus, the corresponding reaction to that given in Step 1 for air is
C5H12 + 8O2 + 30.1N2 5CO2 +6H2O + 30.1N2
3. Determine the amount of air required for combustion, assuming air contains 23.15%oxygen by weight
O2 required =256
72 (2000lb / ton) = 7111lb / ton
Air required =7111lb/ ton
0.2315= 30,717 lb/ ton
4. The amount of air required for combustion can also be computed using the factors, given
previously.
Air required for carbon, C =60
72 (2000lb / ton)11.52 = 19,200lb / ton
Air required for hydrogen, H =12
72 (2000lb / ton) 34.56 = 11,520 lb/ ton
Totalair required = 19,200 +11,520 = 30,720lb / ton
5. Determine the volume of air required for combustion.
Volume of air = (30,717 lb/ton)/(0.075 lb/ft3) = 409,560 ft3/ton
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Solid waste combustors are designed to operate as either mass-fired units or RDF units. A
mass fired combustor uses commingled, unseparated solid waste with little or no processing.
An RDF unit uses refuse-derived fuel, a processed waste which has had much of the
noncombustible material removed. Approximately 23% of the U.S. units are of this type.
Mass-fired units have some design considerations that may not be important when using
RDF:
The nature of the waste can be quite variable and may contain unsuitable
materials. The crane operator can reject large unsuitable objects or attempt to
blend high- and low-moisture content materials.
Potentially hazardous materials may be contained in the waste. The combustor
design should be such that the risk of damage to equipment and the risk of
injury to personnel will be minimized.
The use of RDF can provide a combustible product that is more consistent and may be
processed (although more expensive) to a pellet or cube form (sometimes called densified
RDF or d-RDF) that can be burned by itself or mixed with other fuels. RDF combustion units
are typically smaller than mass-burn combustors, but some space will be required for the
processing of the fuel. Because of RDF's greater uniformity of materials and heat value, an
RDF combustor burns more efficiently than a mass-burn combustor. Air pollution control is
also