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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