Monday, 28 March 2011 20:20

Occupational Hazards and Controls

Table 1 provides an overview of the types of exposures which may be expected in each area of pulp and paper operations. Although exposures may be listed as specific to certain production processes, exposures to employees from other areas may also occur depending on weather conditions, proximity to sources of exposure, and whether they work in more than one process area (e.g., quality control, general labour pool and maintenance personnel).

Table 1. Potential health and safety hazards in pulp and paper production, by process area

Process area

Safety hazards

Physical hazards

Chemical hazards

Biological hazards

Wood preparation

       

Log pond

Drowning; mobile equipment;
slipping, falling

Noise; vibration; cold; heat

Engine exhaust

 

Wood room

Nip points; slipping, falling

Noise; vibration

Terpenes and other wood extracts; wood dust

Bacteria; fungi

Chip screening

Nip points; slipping, falling

Noise; vibration

Terpenes and other wood extracts; wood dust

Bacteria; fungi

Chip yard

Nip points; mobile equipment

Noise; vibration; cold; heat

Engine exhaust; terpenes and other wood extracts; wood dust

Bacteria; fungi

Pulping

       

Stone groundwood
pulping

Slipping, falling

Noise; electric and magnetic fields; high humidity

   

RMP, CMP, CTMP

Slipping, falling

Noise; electric and magnetic fields; high humidity

Cooking chemicals and by-products; terpenes and other wood extracts; wood dust

 

Sulphate pulping

Slipping, falling

Noise; high humidity; heat

Acids and alkalis; cooking chemicals and by-products; reduced sulphur gases; terpenes
and other wood extracts; wood dust

 

Sulphate recovery

Explosions; nip points; slipping,
falling

Noise; heat; steam

Acids and alkalis; asbestos; ash; cooking chemicals and by-products; fuels; reduced
sulphur gases; sulphur dioxide

 

Sulphite pulping

Slipping, falling

Noise; high humidity; heat

Acids and alkalis; cooking chemicals and by-products; sulphur dioxide; terpenes and other wood extracts; wood dust

 

Sulphite recovery

Explosions; nip points; slipping,
falling

Noise; heat; steam

Acids and alkalis; asbestos; ash; cooking chemicals and by-products; fuels; sulphur dioxide

 

Repulping/de-inking

Slipping, falling

 

Acids and alkalis; bleaching chemicals and by- products; dyes and inks; pulp/paper dust; slimicides; solvents

Bacteria

Bleaching

Slipping, falling

Noise; high humidity; heat

Bleaching chemicals and by-products; slimicides; terpenes and other wood extracts

 

Sheet forming and
converting

       

Pulp machine

Nip points; slipping, falling

Noise; vibration; high
humidity; heat; steam

Acids and alkalis; bleaching chemicals and by-products; flocculant; pulp/paper dust; slimicides; solvents

Bacteria

Paper machine

Nip points; slipping, falling

Noise; vibration; high
humidity; heat; steam

Acids and alkalis; bleaching chemicals and by-products; dyes and inks; flocculant; pulp/paper
dust; paper additives; slimicides; solvents

Bacteria

Finishing

Nip points; mobile equipment

Noise

Acids and alkalis; dyes and inks; flocculant;
pulp/paper dust; paper additives; slimicides; solvents

 

Warehouse

Mobile equipment

 

Fuels; engine exhaust; pulp/paper dust

 

Other operations

       

Power generation

Nip points; slipping, falling

Noise; vibration; electric and
magnetic fields; heat; steam

Asbestos; ash; fuels; terpenes and other wood extracts; wood dust

Bacteria; fungi

Water treatment

Drowning

 

Bleaching chemicals and by-products

Bacteria

Effluent treatment

Drowning

 

Bleaching chemicals and by-products; flocculant; reduced sulphur gases

Bacteria

Chlorine dioxide
generation

Explosions; slipping, falling

 

Bleaching chemicals and by-products

Bacteria

Turpentine recovery

Slipping, falling

 

Cooking chemicals and by-products; reduced sulphur gases; terpenes and other wood extracts

 

Tall oil production

   

Acids and alkalis; cooking chemicals and by-products; reduced sulphur gases; terpenes and other wood extracts

 

RMP = refining mechanical pulping; CMP = chemi-mechanical pulping; CTMP = chemi-thermomechanical pulping.

 

Exposure to the potential hazards listed in table 1 is likely to depend on the extent of automation of the plant. Historically, industrial pulp and paper production was a semi-automatic process which required a great deal of manual intervention. In such facilities, operators would sit at open panels adjacent to the processes to view the effects of their actions. The valves at the top and bottom of a batch digester would be manually opened, and during the filling stages, gases in the digester would be displaced by the incoming chips (figure 1). Chemical levels would be adjusted based on experience rather than sampling, and process adjustments would be dependent on the skill and knowledge of the operator, which at times led to upsets. For example, over-chlorination of pulp would expose workers downstream to increased levels of bleaching agents. In most modern mills, progress from manually controlled to electronically controlled pumps and valves allows for remote operation. The demand for process control within narrow tolerances has required computers and sophisticated engineering strategies. Separate control rooms are used to isolate the electronic equipment from the pulp and paper production environment. Consequently, operators usually work in air-conditioned control rooms which offer refuge from the noise, vibration, temperature, humidity and chemical exposures inherent to mill operations. Other controls which have improved the working environment are described below.

Figure 1. Worker opening cap on manually controlled batch digester.

PPI100F1

MacMillan Bloedel archives

Safety hazards including nip points, wet walking surfaces, moving equipment and heights are common throughout pulp and paper operations. Guards around moving conveyors and machinery parts, quick clean-up of spills, walking surfaces which allow drainage, and guard-rails on walkways adjacent to production lines or at height are all essential. Lock-out procedures must be followed for maintenance of chip conveyors, paper machine rolls and all other machinery with moving parts. Mobile equipment used in chip storage, dock and shipping areas, warehousing and other operations should have roll-over protection, good visibility and horns; traffic lanes for vehicles and pedestrians should be clearly marked and signed.

Noise and heat are also ubiquitous hazards. The major engineering control is operator enclosures, as described above, usually available in wood preparation, pulping, bleaching and sheet-forming areas. Air-conditioned enclosed cabs for mobile equipment used in chip pile and other yard operations are also available. Outside these enclosures, workers usually require hearing protection. Work in hot process or outdoor areas and in vessel maintenance operations requires workers to be trained to recognize symptoms of heat stress; in such areas, work scheduling should allow acclimatization and rest periods. Cold weather may create frostbite hazards in outdoor jobs, as well as foggy conditions near chip piles, which remain warm.

Wood, its extracts and associated micro-organisms are specific to wood preparation operations and the initial stages of pulping. Control of exposures will depend on the particular operation, and may include operator booths, enclosure and ventilation of saws and conveyors, as well as enclosed chip storage and low chip inventory. Use of compressed air to clear wood dust creates high exposures and should be avoided.

Chemical pulping operations present the opportunity for exposures to digestion chemicals as well as gaseous by-products of the cooking process, including reduced (kraft pulping) and oxidized (sulphite pulping) sulphur compounds and volatile organics. Gas formation may be influenced by a number of operating conditions: the wood species used; the quantity of wood pulped; the amount and concentration of white liquor applied; the amount of time required for pulping; and maximum temperature attained. In addition to automatic digester capping valves and operator control rooms, other controls for these areas include local exhaust ventilation at batch digesters and blow tanks, capable of venting at the rate the vessel’s gases are released; negative pressure in recovery boilers and sulphite-SO2 acid towers to prevent gas leaks; ventilated full or partial enclosures over post-digestion washers; continuous gas monitors with alarms where leaks may occur; and emergency response planning and training. Operators taking samples and conducting tests should be aware of the potential for acid and caustic exposure in process and waste streams, and the possibility of side reactions such as hydrogen sulphide gas (H2S) production if black liquor from kraft pulping comes into contact with acids (e.g., in sewers).

In chemical recovery areas, acidic and alkaline process chemicals and their by-products may be present at temperatures in excess of 800°C. Job responsibilities may require workers to come into direct contact with these chemicals, making heavy duty clothing a necessity. For example, workers rake the spattering molten smelt that collects at the base of the boilers, thereby risking chemical and thermal burns. Workers may be exposed to dust when sodium sulphate is added to concentrated black liquor, and any leak or opening will release noxious (and potentially fatal) reduced sulphur gases. The potential for a smelt water explosion always exists around the recovery boiler. Water leaks in the tube walls of the boiler have resulted in several fatal explosions. Recovery boilers should be shut down at any indication of a leak, and special procedures should be implemented for transferring the smelt. Loading of lime and other caustic materials should be done with enclosed and ventilated conveyors, elevators and storage bins.

In bleach plants, field operators may be exposed to the bleaching agents as well as chlorinated organics and other by-products. Process variables such as bleaching chemical strength, lignin content, temperature and pulp consistency are constantly monitored, with operators collecting samples and performing laboratory tests. Because of the hazards of many of the bleaching agents used, continuous alarm monitors should be in place, escape respirators should be issued to all employees, and operators should be trained in emergency response procedures. Canopy enclosures with dedicated exhaust ventilation are standard engineering controls found at the top of each bleaching tower and washing stage.

Chemical exposures in the machine room of a pulp or paper mill include chemical carry-over from the bleach plant, the papermaking additives and the chemical mixture in the waste water. Dusts (cellulose, fillers, coatings) and exhaust fumes from mobile equipment are present in the dry-end and the finishing operations. Cleaning between product runs may be done with solvents, acids and alkalis. Controls in this area may include complete enclosure over the sheet drier; ventilated enclosure of the areas where additives are unloaded, weighed and mixed; use of additives in liquid rather than powder form; use of water-based rather than solvent-based inks and dyes; and eliminating the use of compressed air to clean up trimmed and waste paper.

Paper production in recycled paper plants is generally dustier than conventional paper production using newly produced pulp. Exposure to micro-organisms can occur from the beginning (paper collection and separation) to the end (paper production) of the production chain, but exposure to chemicals is less important than in conventional paper production.

Pulp and paper mills employ an extensive maintenance group to service their process equipment, including carpenters, electricians, instrument mechanics, insulators, machinists, masons, mechanics, millwrights, painters, pipefitters, refrigeration mechanics, tinsmiths and welders. Along with their trade-specific exposures (see the Metal processing and metal working and Occupations chapters), these tradespeople may be exposed to any of the process-related hazards. As mill operations have become more automated and enclosed, the maintenance, cleaning and quality assurance operations have become the most highly exposed. Plant shutdowns to clean vessels and machines are of special concern. Depending on mill organization, these operations may be carried out by in-house maintenance or production personnel, although subcontracting to non-mill personnel, who may have less occupational health and safety support services, is common.

In addition to process exposures, pulp and paper mill operations entail some noteworthy exposures for maintenance personnel. Because pulping, recovery and boiler operations involve high heat, asbestos was used extensively to insulate pipes and vessels. Stainless steel is often used in vessels and pipes throughout pulping, recovery and bleaching operations, and to some extent in papermaking. Welding this metal is known to generate chromium and nickel fumes. During maintenance shut-downs, chromium-based sprays may be applied to protect the floor and walls of recovery boilers from corrosion during start-up operations. Process quality measurements in the production line are often made using infrared and radio-isotope gauges. Although the gauges are usually well shielded, instrument mechanics who service them may be exposed to radiation.

Some special exposures may also occur among employees in other mill-support operations. Power boiler workers handle bark, waste wood and sludge from the effluent treatment system. In older mills, workers remove ash from the bottom of the boilers and then reseal the boilers by applying a mixture of asbestos and cement around the boiler grate. In modern power boilers, this process is automated. When material is fed into the boiler at too high a moisture level, workers may be exposed to blow-backs of incomplete combustion products. Workers responsible for water treatment may be exposed to chemicals such as chlorine, hydrazine and various resins. Because of the reactivity of ClO2, the ClO2 generator is usually located in a restricted area and the operator is stationed in a remote control room with excursions to collect samples and service the saltcake filter. Sodium chlorate (a strong oxidizer) used to generate ClO2 can become dangerously flammable if it is allowed to spill on any organic or combustible material and then dry. All spills should be wetted down before any maintenance work may proceed, and all equipment should be thoroughly cleaned afterward. Wet clothing should be kept wet and separate from street clothing, until washed.

 

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Monday, 28 March 2011 20:19

Chemical and By-product Production

Because many bleaching chemicals are reactive and hazardous to transport, they are produced on-site or nearby. Chlorine dioxide (ClO2), sodium hypochlorite (NaOCl) and peracids are always produced on-site, while chlorine (Cl2) and sodium hydroxide or caustic (NaOH) are usually produced off-site. Tall oil, a product derived from the resin and fatty acids that are extracted during kraft cooking, may be refined on- or off-site. Turpentine, a lighter fraction kraft by-product, is often collected and concentrated on-site, and refined elsewhere.

Chlorine Dioxide

Chlorine dioxide (ClO2) is a highly reactive greenish-yellow gas. It is toxic and corrosive, explodes at high concentrations (10%) and is quickly reduced to Cl2 and O2 in the presence of ultraviolet light. It must be prepared as a dilute gas and stored as a dilute liquid, making bulk transport impossible.

ClO2 is generated by reducing sodium chlorate (Na2ClO3) with either SO2, methanol, salt or hydrochloric acid. The gas leaving the reactor is condensed and stored as a 10% liquid solution. Modern ClO2 generators operate at 95% efficiency or greater, and the small amount of Cl2 that is produced will be collected or scrubbed out of the vent gas. Side reactions may occur depending on the purity of the feed chemicals, the temperature and other process variables. By-products are returned to the process and spent chemicals are neutralized and sewered.

Sodium Hypochlorite

Sodium hypochlorite (NaOCl) is produced by combining Cl2 with a dilute solution of NaOH. It is a simple, automated process that requires almost no intervention. The process is controlled by maintaining the caustic concentration such that the residual Cl2 in the process vessel is minimized.

Chlorine and Caustic

Chlorine (Cl2), used as a bleaching agent since the early 1800s, is a highly reactive, toxic, green-coloured gas which becomes corrosive when moisture is present. Chlorine is usually manufactured by the electrolysis of brine (NaCl) into Cl2 and NaOH at regional installations, and transported to the customer as a pure liquid. Three methods are used to produce Cl2 on an industrial scale: the mercury cell, the diaphragm cell, and the most recent development, the membrane cell. Cl2 is always produced at the anode. It is then cooled, purified, dried, liquefied and transported to the mill. At large or remote pulp mills, local facilities may be constructed, and the Cl2 can be transported as a gas.

The quality of NaOH depends on which of the three processes is used. In the older mercury cell method, the sodium and mercury combine to form an amalgam that is decomposed with water. The resulting NaOH is nearly pure. One of the shortcomings of this process is that mercury contaminates the workplace and has resulted in serious environmental problems. The NaOH produced from the diaphragm cell is removed with the spent brine and concentrated to allow the salt to crystallize and separate. Asbestos is used as the diaphragm. The purest NaOH is produced in membrane cells. A semi-permeable resin-based membrane allows sodium ions to pass through without the brine or chlorine ions, and combine with water added to the cathode chamber to form pure NaOH. Hydrogen gas is a by-product of each process. It is usually treated and used either in other processes or as fuel.

Tall Oil Production

Kraft pulping of highly-resinous species such as pine produces sodium soaps of resin and fatty acids. The soap is collected from black liquor storage tanks and from soap skimming tanks that are located in the evaporator train of the chemical recovery process. Refined soap or tall oil can be used as a fuel additive, dust control agent, road stabilizer, pavement binder and roofing flux.

At the processing plant, soap is stored in primary tanks to allow the black liquor to settle to the bottom. The soap rises and overflows into a second storage tank. Sulphuric acid and the decanted soap are fed into a reactor, heated to 100°C, agitated and then allowed to settle. After settling overnight, the crude tall oil is decanted into a storage vessel and allowed to sit for another day. The top fraction is considered dry crude tall oil and is pumped to storage, ready for shipment. The cooked lignin in the bottom fraction will become part of the subsequent batch. The spent sulphuric acid is pumped to a storage tank, and any entrained lignin is allowed to settle to the bottom. The lignin left in the reactor is concentrated for several cooks, dissolved in 20% caustic and returned to the primary soap tank. Periodically, the collected black liquor and the residual lignin from all sources are concentrated and burned as fuel.

Turpentine Recovery

Gases from the digesters and condensate from black liquor evaporators may be collected for recovery of turpentine. The gases are condensed, combined, then stripped of turpentine, which is recondensed, collected and sent to a decanter. The top fraction of the decanter is drawn off and sent to storage, while the bottom fraction is recycled to the stripper. Raw turpentine is stored separately from the rest of the collection system because it is noxious and flammable, and is usually processed off-site. All the non-condensable gases are collected and incinerated either in the power boilers, the lime kiln or a dedicated furnace. The turpentine can be processed for use in camphor, synthetic resins, solvents, flotation agents and insecticides.

 

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Monday, 28 March 2011 20:18

Power Generation and Water Treatment

In addition to liquor recovery, pulp mills recover a significant portion of energy from burning waste materials and by-products of the process in power boilers. Materials such as bark, wood waste and dried sludge collected from effluent treatment systems may be burned to provide steam to power electrical generators.

Pulp and paper mills consume vast amounts of fresh water. A 1,000 tonne per day bleached kraft pulp mill may use more than 150 million litres of water a day; a paper mill even more. In order to prevent adverse effects on mill equipment and to maintain product quality, the incoming water must be treated to remove contaminants, bacteria and minerals. Several treatments are applied depending on the quality of the incoming water. Sedimentation beds, filters, flocculants, chlorine and ion exchange resins are all used to treat water before it is used in the process. Water that is used in the power and recovery boilers is further treated with oxygen scavengers and corrosion inhibitors such as hydrazine and morpholine to avoid deposits forming in the boiler tubes, to reduce metal corrosion, and to prevent carry-over of water to the steam turbine.

 

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End products of pulp and paper mills depend on the pulping process, and may include market pulp and various types of paper or paperboard products. For example, the relatively weak mechanical pulp is converted into single-use products such as newspapers and tissue. Kraft pulp is converted into multi-use paper products such as high-quality writing paper, books and grocery bags. Sulphite pulp, which is primarily cellulose, can be used in a series of diverse end-products including specialty paper, rayon, photographic film, TNT, plastics, adhesives, and even ice cream and cake mixes. Chemi-mechanical pulps are exceptionally stiff, ideal for the structural support needed for corrugated container board. The fibres in pulp from recycled paper are usually shorter, less flexible and less water permeable, and can therefore not be used for high-quality paper products. Recycled paper is therefore mainly used for the production of soft paper products like tissue paper, toilet paper, paper towelling and napkins.

To produce market pulp, the pulp slurry is usually screened once more and its consistency adjusted (4 to 10%) before it is ready for the pulp machine. The pulp is then spread onto a travelling metal screen or plastic mesh (known as the “wire”) at the “wet end” of the pulp machine, where the operator monitors the speed of the moving wire and the water content of the pulp (figure 1; the presses and the cover of the drier can be seen in the upper left; in modern mills, operators spend a great deal of time in control rooms). Water and filtrate are drawn through the wire, leaving a web of fibres. The pulp sheet is passed through a series of rotating rolls (“presses”) that squeeze out water and air until the fibre consistency is 40 to 45%. The sheet is then floated through a multi-storey sequence of hot-air dryers until the consistency is 90 to 95%. Finally, the continuous pulp sheet is cut into pieces and stacked into bales. The pulp bales are compressed, wrapped and packaged into bundles for storage and transport.

Figure 1. Wet end of pulp machine showing fibre mat on the wire.

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Canfor Library

Although similar in principle to making pulp sheets, paper making is considerably more complex. Some mills use a variety of different pulps to optimize paper quality (e.g., a mix of hardwood, softwood, kraft, sulphite, mechanical or recycled pulps). Depending on the type of pulp used, a series of steps is necessary prior to forming the paper sheet. Generally, dried market pulp is rehydrated, while high-consistency pulp from storage is diluted. Pulp fibres may be beaten to increase the fibre-bonding area and thereby improve paper sheet strength. The pulp is then blended with “wet-end” additives (table 1) and passed through a final set of screens and cleaners. The pulp is then ready for the paper machine.

Table 1. Papermaking additives

Additive

Location applied

Purpose and/or examples of specific agents

Most commonly used additives

Talc

Wet end

Pitch control (prevent deposition and accumulation
of pitch)
Filler (make brighter, smoother, more opaque)

Titanium dioxide

Wet end

Pigment (brighten sheet, improve printing)
Filler (make brighter, smoother, more opaque)

“Alum”(Al2(SO4)3)

Wet end

Precipitates rosin sizing onto fibres
Retention aid (fix additives to fibres, improve pulp
fibre retention)

Rosin

Wet end

Internal sizing (resist liquid penetration)

Clay (kaolin)

Wet/dry

Filler (make brighter, smoother, more opaque)
Pigment or surface coating (impart colour)

Starch

Wet/dry

Surface sizing (resist liquid penetration)
Dry strength additive (increase strength, reduce
surface lint)
Retention aid (bind additives to paper, improve
pulp fibre retention)

Dyes and
pigments

Wet/dry

e.g., acid, basic or direct dyes,colour lakes,
CaCO3, may also include solvent vehicles

Latex

Dry end

Adhesive (reinforce sheet, bind additives to paper,
fill pores)
Waterproofing (resist liquid penetration)

Other additives

Slimicides

Wet end

e.g., thiones, thiazoles, thiocyanates, hiocarbamates, thiols, isothiazolinones,
formaldehyde, glutaraldehyde, glycols, naphthol,
chlorinated and brominated organics, organic
mercury compounds

Defoamers

Wet end

e.g., pine oil, fuel oil, recycled oils, silicones, alcohols

Wire treatment
agents

Wet end

e.g., imidazoles, butyl diglycol, acetone, turpentine,
phosphoric acid

Wet and dry
strength additives

Wet end

e.g., formaldehyde resins, epichlorohydrin, glyoxal,
gums, polyamines, phenolics,
polyacrylamides, polyamids, cellulose derivatives

Coatings,
adhesives and
plasticizers

Dry end

e.g., aluminium hydroxide, polyvinyl acetate,
acrylics, linseed oil, gums, protein glues, wax
emulsions, azite, glyoxal, stearates, solvents,
polyethylene, cellulose derivatives, foil, rubber
derivatives, polyamines, polyesters,
butadiene-styrene polymers

Others

Wet/dry

Corrosion inhibitors, dispersants, flameproofing,
antitarnish agents, drainage aids, deflocculants, pH
control agents, preservatives

 

The flow spreader and headbox distribute a thin suspension (1 to 3%) of refined pulp onto a moving wire (similar to a pulp machine, only at a much higher speed, sometimes in excess of 55 km/h) which forms the fibres into a thin felted sheet. The sheet moves through a series of press rolls to the dryer section, where a series of steam-heated rolls evaporate most of the remaining water. Hydrogen bonds between the fibres have fully developed at this stage. Finally, the paper is calendered and reeled. Calendering is the process by which the paper surface is ironed smooth and its thickness reduced. The dried, calendered paper sheet is wound onto a reel, labelled and transported to the warehouse (figure 2; note waste paper under reel, and unenclosed operator control panel). “Dry-end” additives can be added before calendering on the paper machine or in separate “off-machine” coating operations in the converting sector of the industry.

Figure 2. Dry end of a paper machine showing full paper reel and operator using air slitter to cut end.

PPI070F2

George Astrakianakis

A variety of chemicals are used in the papermaking process to provide the paper with specific surface characteristics and sheet properties. The most commonly used additives (table 1) are typically used at the per cent level, though some such as clay and talc may contribute as much as 40% to the dry weight of certain papers. Table 1 also indicates the diversity of chemical additives which may be used for specific production purposes and products; some of these are used at very low concentrations (e.g., slimicides are added to process water in parts per million).

The process of making paperboard is similar to that of making paper or pulp. A suspension of pulp and water is dispersed onto a travelling wire, the water is removed, and the sheet dried and stored as a roll. The process differs in the way that the sheet is formed to give thickness, in the combining of multiple layers, and in the drying process. Board can be made from single or multi-layered sheets with or without a core. The sheets are usually high-quality kraft pulp (or kraft and CTMP blend), while the core is made from either a blend of semi-chemical and low-cost recycled pulp or from entirely recycled pulp and other waste material. Coatings, vapour barriers and multiple layers are added according to the end use to protect the contents from water and physical damage.

 

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Monday, 28 March 2011 20:15

Recycled Paper Operations

The use of waste or recycled paper as the raw material for pulp production has increased during the last several decades, and some paper plants depend almost completely on waste paper. In some countries, waste paper is separated from other household waste at the source before it is collected. In other countries separation by grade (e.g., corrugated board, newsprint, high-grade paper, mixed) takes place in special recycling plants.

Recycled paper can be repulped in a relatively mild process which uses water and sometimes NaOH. Small metal pieces and plastics may be separated during and/or after repulping, using a debris rope, cyclones or centrifugation. Filling agents, glues and resins are removed in a cleaning stage by blowing air through the pulp slurry, sometimes with the addition of flocculating agents. The foam contains the unwanted chemicals and is removed. The pulp can be de-inked using a series of washing steps which may or may not include the use of chemicals (i.e., surfactant fatty acid derivatives) to dissolve remaining impurities, and bleaching agents to whiten the pulp. Bleaching has the disadvantage that it may reduce fibre length and therefore lessen final paper quality. The bleaching chemicals used in recycled pulp production are usually similar to those used in brightening operations for mechanical pulps. After the repulping and de-inking operations, sheet production follows in a manner very similar to that using virgin fibre pulp.

 

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Monday, 28 March 2011 20:13

Bleaching

Bleaching is a multi-stage process that refines and brightens raw pulp. The objective is to dissolve (chemical pulps) or modify (mechanical pulps) the brown-coloured lignin that was not removed during pulping, while maintaining the integrity of the pulp fibres. A mill produces customized pulp by varying the order, concentration and reaction time of the bleaching agents.

Each bleaching stage is defined by its bleaching agent, pH (acidity), temperature and duration (table 1). After each bleaching stage, the pulp may be washed with caustic to remove spent bleaching chemicals and dissolved lignin before it progresses to the next stage. After the last stage, the pulp is pumped through a series of screens and cleaners to remove any contaminants such as dirt or plastic. It is then concentrated and conveyed to storage.

Table 1. Bleaching agents and their conditions of use

 

Symbol

Concentration
of agent (%)

pH

Consistency*
(%)

Temperature
(°C)

Time (h)

Chlorine (Cl2)

C

2.5–8

2

3

20–60

0.5–1.5

Sodium hydroxide (NaOH)

E

1.5–4.2

11

10–12

<80

1–2

Chlorine dioxide (ClO2)

D

~1

0–6

10–12

60–75

2–5

Sodium hypochlorite (NaOCl)

H

1–2

9–11

10–12

30–50

0.5–3

Oxygen (O2)

O

1.2–1.9

7–8

25–33

90–130

0.3–1

Hydrogen peroxide (H2O2)

P

0.25

10

12

35–80

4

Ozone (O3)

Z

0.5–3.5

2–3

35–55

20–40

<0.1

Acid washing (SO2)

A

4–6

1.8–5

1.5

30–50

0.25

Sodium dithionite (NaS2O4)

Y

1–2

5.5–8

4–8

60–65

1–2

* Concentration of fibre in water solution.

Historically, the most common bleaching sequence used to produce market-grade bleached kraft pulp is based on the five-stage CEDED process (see table 1 for definition of symbols). The first two stages of bleaching complete the delignification process and are considered extensions of pulping. Because of environmental concerns about chlorinated organics in pulp mill effluents, many mills substitute chlorine dioxide (ClO2) for a portion of the chlorine (Cl2) used in the first bleaching stage (CDEDED) and use oxygen (O2) pre-treatment during the first caustic extraction (CDEODED). The current trend in Europe and North America is towards complete substitution with ClO2 (e.g., DEDED) or elimination of both Cl2 and ClO2. Where ClO2 is used, sulphur dioxide (SO2) is added during the final washing stage as an “antichlor” to stop the ClO2 reaction and to control the pH. Newly developed chlorine-free bleaching sequences (e.g., OAZQP, OQPZP, where Q = chelation) use enzymes, O2, ozone (O3), hydrogen peroxide (H2O2), peracids and chelating agents such as ethylene diamine tetracetic acid (EDTA). Totally chlorine-free bleaching had been adopted at eight mills worldwide by 1993. Because these newer methods eliminate the acidic bleaching steps, acid washing is a necessary addition to the initial stages of kraft bleaching to allow removal of metals bound to the cellulose.

Sulphite pulps are generally easier to bleach than kraft pulps because of their lower lignin content. Short bleaching sequences (e.g., CEH, DCEHD, P, HP, EPOP) can be used for most paper grades. For dissolving-grade sulphite pulps used in the production of rayon, cellophane and so on, both hemicellulose and lignin are removed, requiring more complex bleaching sequences (e.g., C1C2ECHDA). The final acid wash is both for metal control and antichlor purposes. The effluent load for dissolving-grade sulphite pulps is much greater because so much of the raw wood is consumed (typical yield 50%) and more water is used.

The term brightening is used to describe bleaching of mechanical and other high-yield pulps, because they are whitened by destroying chromophoric groups without dissolving the lignin. Brightening agents include H2O2 and/or sodium hydrosulphite (NaS2O4). Historically, zinc hydrosulphite (ZnS2O4) was commonly used, but has been largely eliminated because of its toxicity in effluent. Chelating agents are added before bleaching to neutralize any metal ions, thereby preventing the formation of coloured salts or the decomposition of H2O2. The effectiveness of mechanical pulp bleaching depends on the species of wood. Hardwoods (e.g., poplar and cottonwood) and softwoods (e.g., spruce and balsam) that are low in lignin and extractives can be bleached to a higher brightness level than the more resinous pine and cedar.

 

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Monday, 28 March 2011 20:09

Pulping

Pulping is the process by which the bonds within the wood structure are ruptured either mechanically or chemically. Chemical pulps can be produced by either alkaline (i.e., sulphate or kraft) or acidic (i.e., sulphite) processes. The highest proportion of pulp is produced by the sulphate method, followed by mechanical (including semi-chemical, thermomechanical and mechanical) and sulphite methods (figure 1). Pulping processes differ in the yield and quality of the product, and for chemical methods, in the chemicals used and the proportion that can be recovered for reuse.

Figure 1. Worldwide pulp capacities, by pulp type

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Mechanical Pulping

Mechanical pulps are produced by grinding wood against a stone or between metal plates, thereby separating the wood into individual fibres. The shearing action breaks cellulose fibres, so that the resulting pulp is weaker than chemically separated pulps. The lignin connecting cellulose to hemicellulose is not dissolved; it merely softens, allowing the fibres to be ground out of the wood matrix. The yield (proportion of original wood in pulp) is usually greater than 85%. Some mechanical pulping methods also use chemicals (i.e., the chemi-mechanical pulps); their yields are lower since they remove more of the non-cellulosic materials.

In stone groundwood pulping (SGW), the oldest and historically most common mechanical method, fibres are removed from short logs by pressing them against a rotating abrasive cylinder. In refiner mechanical pulping (RMP, figure 2), which gained popularity after it became commercially viable in the 1960s, wood chips or sawdust are fed through the centre of a disc refiner, where they are shredded into finer pieces as they are pushed out through progressively narrower bars and grooves. (In figure 2, the refiners are enclosed in the middle of the picture and their large motors are on the left. Chips are supplied though the large diameter pipes, and pulp exits the smaller ones.) A modification of RMP is thermomechanical pulping (TMP), in which the chips are steamed before and during refining, usually under pressure.

Figure 2. Refiner mechanical pulping

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One of the earliest methods of producing chemi-mechanical pulps involved pre-steaming logs before boiling them in chemical pulping liquors, then grinding them in stone grinders to produce “chemi-groundwood” pulps. Modern chemi-mechanical pulping uses disc refiners with chemical treatment (e.g., sodium bisulphite, sodium hydroxide) either prior to, during or after refining. Pulps produced in this manner are referred to either as chemi-mechanical pulps (CMP) or chemi-thermomechanical pulps (CTMP), depending on whether refining was carried out at atmospheric or elevated pressure. Specialized variations of CTMP have been developed and patented by a number of organizations.

Chemical Pulping and Recovery

Chemical pulps are produced by chemically dissolving the lignin between the wood fibres, thereby enabling the fibres to separate relatively undamaged. Because most of the non-fibrous wood components are removed in these processes, yields are usually in the order of 40 to 55%.

In chemical pulping, chips and chemicals in aqueous solution are cooked together in a pressure vessel (digester, figure 3) which can be operated on a batch or continuous basis. In batch cooking, the digester is filled with chips through a top opening, the digestion chemicals are added, and the contents cooked at elevated temperature and pressure. Once the cook is complete, the pressure is released, “blowing” the delignified pulp out of the digester and into a holding tank. The sequence is then repeated. In continuous digesting, pre-steamed chips are fed into the digester at a continuous rate. Chips and chemicals are mixed together in the impregnation zone at the top of the digester and then proceed through the upper cooking zone, the lower cooking zone, and the washing zone before being blown into the blow tank.

Figure 3. Continuous kraft digestor, with chip conveyor under construction

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The digesting chemicals are recovered in most chemical pulping operations today. The principal objectives are to recover and reconstitute digestion chemicals from the spent cooking liquor, and to recover heat energy by burning the dissolved organic material from the wood. The resulting steam and electricity supplies some, if not all, of the mill’s energy needs.

Sulphate Pulping and Recovery

The sulphate process produces a stronger, darker pulp than other methods and requires chemical recovery to compete economically. The method evolved from soda pulping (which uses only sodium hydroxide for digestion) and began to gain prominence in the industry from the 1930s to 1950s with the development of chlorine dioxide bleaching and chemical recovery processes, which also produced steam and power for the mill. The development of corrosion-proof metals, such as stainless steel, to handle the acidic and alkaline pulp mill environments also played a role.

The cooking mixture (white liquor) is sodium hydroxide (NaOH, “caustic”) and sodium sulphide (Na2S). Modern kraft pulping is usually carried out in continuous digesters often lined with stainless steel (figure 3). The temperature of the digester is raised slowly to approximately 170°C and held at that level for approximately 3 to 4 hours. The pulp (called brown stock because of its colour) is screened to remove uncooked wood, washed to remove the spent cooking mixture (now black liquor), and sent either to the bleach plant or to the pulp machine room. Uncooked wood is either returned to the digester or sent to the power boiler to be burned.

The black liquor collected from the digester and brown stock washers contains dissolved organic material whose exact chemical composition depends on the wood species pulped and the cooking conditions. The liquor is concentrated in evaporators until it contains less than 40% water, then sprayed into the recovery boiler. The organic component is consumed as fuel, generating heat which is recovered in the upper section of the furnace as high-temperature steam. The unburned inorganic component collects at the bottom of the boiler as a molten smelt. The smelt flows out of the furnace and is dissolved in a weak caustic solution, producing “green liquor” containing primarily dissolved Na2S and sodium carbonate (Na2CO3). This liquor is pumped to a recausticizing plant, where it is clarified, then reacted with slaked lime
(Ca(OH)2), forming NaOH and calcium carbonate (CaCO3). The white liquor is filtered and stored for subsequent use. CaCO3 is sent to a lime kiln, where it is heated to regenerate lime (CaO).

 

Sulphite Pulping and Recovery

Sulphite pulping dominated the industry from the late 1800s to the mid-1900s, but the method used during this era was limited by the types of wood which could be pulped and the pollution created by discharging untreated waste cooking liquor into waterways. Newer methods have overcome many of these problems, but sulphite pulping is now a small segment of the pulp market. Although sulphite pulping usually uses acid digestion, both neutral and basic variations exist.

The cooking liquor of sulphurous acid (H2SO3) and bisulphite ion (HSO3) is prepared on-site. Elemental sulphur is burned to produce sulphur dioxide (SO2), which is passed up through an absorption tower that contains water and one of four alkaline bases (CaCO3, the original sulphite base, Na2CO3, magnesium hydroxide (Mg(OH)2) or ammonium hydroxide (NH4OH)) which produce the acid and ion and control their proportions. Sulphite pulping is usually carried out in brick-lined batch digesters. To avoid unwanted reactions, the digester is heated slowly to a maximum temperature of 130 to 140°C and the chips are cooked for a long time (6 to 8 hours). As the digester pressure increases, gaseous sulphur dioxide (SO2) is bled off and remixed with the raw cooking acid. When approximately 1 to 1.5 hours of cooking time remains, heating is discontinued and the pressure is decreased by bleeding off gas and steam. The pulp is blown into a holding tank, then washed and screened.

The spent digestion mixture, called red liquor, can be used for heat and chemical recovery for all but calcium-bisulphite-base operations. For ammonia-base sulphite pulping, the dilute red liquor is first stripped to remove residual SO2, then concentrated and burned. The flue gas containing SO2 is cooled and passed through an absorption tower where fresh ammonia combines with it to regenerate the cooking liquor. Finally, the liquor is filtered, fortified with fresh SO2 and stored. The ammonia cannot be recovered because it is converted into nitrogen and water in the recovery boiler.

In magnesium-base sulphite pulping, burning the concentrated pulping liquor gives magnesium oxide (MgO) and SO2, which are easily recovered. No smelt is produced in this process; rather MgO is collected from the flue gas and slaked with water to produce magnesium hydroxide (Mg(OH)2). SO2 is cooled and combined with the Mg(OH)2 in an absorption tower to reconstitute the cooking liquor. The magnesium bisulphite (Mg(HSO3)2) is then fortified with fresh SO2 and stored. Recovery of 80 to 90% of the cooking chemicals is possible.

Recovery of sodium-base sulphite cooking liquor is more complicated. Concentrated spent liquor is incinerated, and approximately 50% of the sulphur is converted into SO2. The remainder of the sodium and sulphur is collected at the bottom of the recovery boiler as a smelt of Na2S and Na2CO3. The smelt is dissolved to produce green liquor, which is converted to sodium bisulphite (NaHSO3) in several steps. The NaHSO3 is fortified and stored. The regeneration process produces reduced sulphur gases, in particular hydrogen sulphide (H2S).

 

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Adapted from Soskolne 1997, with permission.

Hazardous wastes include, among other things, radioactive materials and chemicals. The movement of these substances from their source to other locations has been termed “toxic trade”. It was in the late 1980s that concern was raised about toxic trade, in particular with Africa (Vir 1989). This set the stage for the recently recognized issue of environmental justice, in some situations also known as environmental racism (Coughlin 1996).

Vir (1989) pointed out that as environmental safety laws became increasingly stringent in Europe and in the United States, and as the cost of disposal increased, “dumpers” or “waste merchants” began to turn their attention to poorer nations as potential and willing recipients of their waste products, providing a much needed source of revenue to these poorer countries. Some of these countries had been willing to take such waste at a fraction of the cost that developed nations would otherwise have had to pay for their disposal. To “nations that are drowning economically, this is an attractive deal” (Vir 1989).

Asante-Duah, Saccomanno and Shortreed (1992) show the exponential growth in the United States in the production of hazardous wastes since 1970, with the costs associated with treatment and disposal similarly increasing. They argue in favour of a controlled hazardous waste trade, one that is “regulated and informed”. They note that “countries generating small quantities of hazardous wastes should view the waste trade as an important economic option, as long as the waste recipients do not compromise their environmental sustainability”. Hazardous wastes will continue to be generated and there are countries for which an increase in some of these substances would not increase the risk to health of either present or future generations. It might therefore be economically efficient for such countries to accept waste.

There are others who argue that waste should be disposed of only at the source and not be transported at all (Puckett and Fogel 1994; Cray 1991; Southam News 1994). The latter argue from the position that science is incapable of providing any guarantees about the absence of risk.

One ethical principle that emerges from the foregoing argument is that of respect for autonomy (i.e., respect for persons), which also includes questions of national autonomy. The crucial question is one of the ability of a recipient country to adequately assess the level of risk associated with a shipment of hazardous waste. Assessment presupposes full disclosure of the contents of a shipment from the originating country and a level of local expertise to assess any potential impacts on the recipient country.

Because communities in developing countries are less likely to be informed about the potential risks associated with waste shipments, the NIMBY phenomenon (i.e., not in my backyard) so evident in the more affluent regions of the world is less likely to manifest in poorer regions. Furthermore, workers in developing regions of the world tend not to have the infrastructure related to worker protection, including information concerning the labelling of products with which they come into contact. Hence, workers in poorer nations involved in the management, storage and disposal of hazardous waste would lack the training to know how to protect themselves. Regardless of these ethical considerations, in the final analysis the economic benefits to be derived from accepting such waste shipments would need to be weighed against any potential harms that could arise in the short, medium and longer terms.

A second ethical principle emerging from the preceding argument is that of distributive justice, which involves question regarding who takes risks and who derives benefits. When there is an imbalance between those who take risks and those who derive benefits, the principle of distributive justice is not being honoured. It has often been financially poor labourers who have been exposed to hazards without any ability to enjoy the fruits of their efforts. This has occurred in the context of production of relatively expensive merchandise in the developing world for the benefit of first world markets. Another example related to the testing of new vaccines or drugs on people in developing countries who could never afford access to them in their own countries.

Towards Controlling the Transport of Hazardous Wastes

Because of the recognized need to better control the dumping of hazardous wastes, the Basel Convention was entered into by ministers of 33 countries in March 1989 (Asante-Duah, Saccomanno and Shortreed 1992). The Basel Convention addressed the transboundary movements of hazardous wastes and required the notification and consent of recipient countries before any waste shipments could take place.

Subsequently, the United Nations Environment Programme (UNEP) launched its Cleaner Production Programme, in close cooperation with governments and industry, to advocate low- and non-waste technologies (Rummel-Bulska 1993). In March 1994, a full ban was introduced on all transboundary movements of hazardous wastes from the 24 rich industrialized countries of the Organization for Economic Cooperation and Development (OECD) to other states that are not members of the OECD. The ban was immediate for wastes bound for final disposal and enters into force at the beginning of 1998 for all hazardous wastes that are said to be destined for recycling or recovery operations (Puckett and Fogel 1994). The countries most opposed to the introduction of a total ban were Australia, Canada, Japan and the United States. Despite this opposition from a handful of powerful industrial governments through the penultimate vote, the ban was finally agreed to by consensus (Puckett and Fogel 1994).

Greenpeace has stressed the primary prevention approach to solving the mounting waste crisis by addressing the root cause of the problem, namely minimizing waste generation through clean production technologies (Greenpeace 1994a). In making this point, Greenpeace identified major countries exporting hazardous wastes (Australia, Canada, Germany, the United Kingdom and the United States) and some countries importing them (Bangladesh, China (including Taiwan), India, Indonesia, Malaysia, Pakistan, the Philippines, the Republic of Korea, Sri Lanka and Thailand). In 1993, Canada, for example, had exported some 3.2 million kilograms of ash containing lead and zinc to India, the Republic of Korea and Taiwan, China, and 5.8 million kilograms of plastic waste to Hong Kong (Southam News 1994). Greenpeace (1993, 1994b) also addresses the extent of the problem in terms of specific substances and approaches to disposal.

Risk Assessment

Epidemiology is at the centre of human health risk assessment, which is invoked when concern is raised by a community about the consequences, if any, of exposure to hazardous and potentially toxic substances. The scientific method that epidemiology brings to the study of the environmental determinants of ill health can be fundamental to protecting unempowered communities, both from environmental hazards and from environmental degradation. Risk assessment conducted in advance of a shipment likely would fall into the legal trade arena; when conducted after a shipment has arrived, risk assessment would be undertaken to determine whether or not any health concerns were justified from what likely would have been an illegal shipment.

Among the concerns to the risk assessor would be hazard assessment, i.e., questions about what hazards, if any, exist and in what quantities and in what form they might be present. In addition, depending on the type of hazard, the risk assessor must make an exposure assessment to establish what possibilities there are for people to be exposed to the hazardous substance(s) through inhalation, skin absorption or ingestion (by contamination of the food chain or directly on foodstuffs).

In terms of trade, autonomy would require the informed consent of the parties in a voluntary and non-coercive milieu. However, it is hardly possible that non-coerciveness could ever pertain in such a circumstance by virtue of the financial need of an importing developing world country. The analogue here is the now accepted ethical guideline which does not permit the coercion of participants in research through payment for anything but direct costs (e.g., lost wages) for the time taken to participate in a study (CIOMS 1993). Other ethical issues involved here would include, on the one hand, truth in the presence of unknowns or in the presence of scientific uncertainty and, on the other hand, the principle of caveat emptor (buyer beware). The ethical principle of non-maleficence requires the doing of more good than harm. Here the short-term economic benefits of any trade agreement to accept toxic wastes must be weighed against the longer term damage to the environment, the public health and possibly also to future generations.

Finally, the principle of distributive justice requires recognition by the parties involved in a trade deal as to who would be deriving the benefits and who would be taking the risks in any trade deal. In the past, general practices for dumping waste and for locating hazardous waste sites in unempowered communities in the United States have led to the recognition of the concern now known as environmental justice or environmental racism (Coughlin 1996). In addition, questions of environmental sustainability and integrity have become central concerns in the public forum.

Acknowledgements: Dr. Margaret-Ann Armour, Department of Chemistry, University of Alberta, provided valuable references on the topic of toxic trade as well as materials from the November 1993 Pacific Basin “Conference on Hazardous Waste” at the University of Hawaii.

The Greenpeace office in Toronto, Ontario, Canada, was most helpful in providing copies of the Greenpeace references cited in this article.

 

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Monday, 28 March 2011 20:05

Waste Disposal Operations

Workers involved in municipal waste disposal and handling face occupational health and safety hazards which are as diverse as the materials they are handling. Workers’ primary complaints relate to odour and upper respiratory tract irritation usually related to dust. However, actual occupational health and safety concerns vary with the work process and the waste stream characteristics (mixed municipal solid waste (MSW), sanitary and biological waste, recycled wastes, agricultural and food wastes, ash, construction debris and industrial wastes). Biological agents such as bacteria, endotoxins and fungi may present hazards, particularly for immune system-compromised and hypersensitive workers. In addition to safety concerns, health impacts have involved predominantly respiratory health problems among workers, including symptoms of organic dust toxic syndrome (ODTS), irritation of the skin, eyes and upper airways and cases of more severe pulmonary diseases such as asthma, alveolitis and bronchitis.

The World Bank (Beede and Bloom 1995) estimates that 1.3 billion tonnes of MSW were generated in 1990 which represents an average of two-thirds of a kilogram per person per day. In the US alone, an estimated 343,000 workers were involved in MSW collection, transport and disposal according to 1991 US Census Bureau statistics. In industrialized countries waste streams are increasingly distinct and work processes are increasingly complex. Efforts to segregate and better define the compositions of waste streams are often critical for identifying occupational hazards and appropriate controls and for controlling environmental impacts. Most waste disposal workers continue to face unpredictable exposures and risks from mixed wastes in dispersed open dumps, often with open burning.

The economics of waste disposal, reuse and recycling, as well as public health concerns, are driving rapid changes in waste handling globally to maximize recovery of resources and reduce dispersion of refuse into the environment. Depending on local economic factors this results in the adoption of either increasingly labour-intensive or capital-intensive work processes. Labour-intensive practices draw an increasing number of workers into hazardous work environments and commonly involve informal sector scavengers who sort mixed refuse by hand and sell recyclable and reusable materials. Increased capitalization has not automatically led to improvements in working conditions as increased work within confined spaces (e.g., in drum composting operations or incinerators), and increased mechanical processing of wastes can result in increased exposure to both airborne contaminants and mechanical hazards, unless proper controls are implemented.

Waste Disposal Processes

A variety of waste disposal processes are used, and as waste collection, transportation and disposal costs increase to meet increasingly stringent environmental and community standards, an increasing diversity of processes can be cost-justified. These processes break down into four basic approaches which may be used in combination or in parallel for various waste streams. The four basic processes are dispersal (land or water dumping, evaporation), storage/isolation (sanitary and hazardous waste landfills), oxidation (incineration, composting) and reduction (hydrogenation, anaerobic digestion). These processes share some general occupational hazards associated with waste handling, but also involve work-process-specific occupational hazards.

General Occupational Hazards in Waste Handling

Regardless of the specific disposal process being utilized, simply processing MSW and other wastes involves common defined hazards (Colombi 1991; Desbaumes 1968; Malmros and Jonsson 1994; Malmros, Sigsgaard and Bach 1992; Maxey 1978; Mozzon, Brown and Smith 1987; Rahkonen, Ettala and Loikkanen 1987; Robazzi et al. 1994).

Unidentified, highly hazardous materials are often intermixed with normal waste. Pesticides, flammable solvents, paints, industrial chemicals, and biohazardous waste, may all be intermixed with household waste. This hazard can be handled primarily through segregation of the waste stream and in particular separation of industrial and household waste.

Odours and exposure to mixed volatile organic compounds (VOCs) can induce nausea but are typically well below American Conference of Governmental Industrial Hygenists (ACGIH) threshold limit values (TLVs), even within enclosed spaces (ACGIH 1989; Wilkins 1994). Control typically involves isolation of the process, as in sealed anaerobic digesters or drum composters, minimizing worker contact through daily soil cover or transfer station cleanup and controlling biological degradation processes, particularly minimizing anaerobic degradation by controlling moisture content and aeration.

Insect- and rodent-borne pathogens can be controlled through daily cover of waste with soil. Botros et al. (1989) reported that 19% of garbage workers in Cairo had antibodies to Rickettsia Typhi (from fleas) which causes human rickettsial disease.

Injection or blood contact with infectious waste, such as needles and blood soiled waste, is best controlled at the generator by segregation and sterilization of such waste prior to disposal and disposal in puncture resistant containers. Tetanus is also a real concern should skin damage occur. Up-to-date immunization is required.

Ingestion of Giardia sp. and other gastrointestinal pathogens can be controlled by minimizing handling, reducing hand-to-mouth contact (including tobacco use), supplying safe drinking water, providing toilet and clean up facilities for workers and maintaining appropriate temperature in composting operations in order to destroy pathogens prior to dry handling and bagging. Precautions are particularly appropriate for Giardia found in sewage sludge and disposable baby diapers in MSW, as well as for tape and round worms from poultry and slaughterhouse wastes.

Inhalation of airborne bacteria and fungi is of particular concern when mechanical processing increases (Lundholm and Rylander 1980) with compactors (Emery et al. 1992), macerators or shredders, aeration, bagging operations and when moisture content is allowed to drop. This results in increased respiratory disorders (Nersting et al. 1990), bronchial obstruction (Spinaci et al. 1981) and chronic bronchitis (Ducel et al. 1976). Although there are no formal guidelines, the Dutch Occupational Health Association (1989) recommended that total bacteria and fungal counts should be kept below 10,000 colony forming units per cubic metre (cfu/m3) and below 500 cfu/m3 for any single pathogenic organism (outdoor air levels are about 500 cfu/m3 for total bacteria, indoor air is typically less). These levels may be regularly exceeded in composting operations.

Biotoxins are formed by fungi and bacteria including endotoxins formed by gram-negative bacteria. Inhaling or ingesting an endotoxin, even after killing the bacteria which produced it, can cause fever and flu-like symptoms without infection. The Dutch Working Group on Research Methods in Biological Indoor Air Pollution recommends that airborne gram-negative bacteria be kept below 1000 cfu/m3 to avoid endotoxin effects. Bacteria and fungi can produce a variety of other potent toxins which may also present occupational hazards.

Heat exhaustion and heat stroke can be serious concerns particularly where safe drinking water is limited and where PPE is utilized in sites known to contain hazardous wastes. Simple PVC-Tyvek suits show a heat stress equivalent of adding 6 to 11°C (11 to 20°F) to the ambient wet bulb globe temperature (WBGT) index (Paull and Rosenthal 1987). When the WBGT exceeds 27.7°C (82°F) conditions are considered hazardous.

Skin damage or disease are common complaints in waste handling operations (Gellin and Zavon 1970). Direct skin damage from caustic ash and other irritating waste contaminants, combined with high exposures to pathogenic organisms, frequent skin lacerations and punctures and, typically, poor availability of washing facilities result in a high incidence of skin problems.

Wastes contain a variety of materials that can cause lacerations or punctures. These are of particular concern in labour intensive operations such as waste sorting for recycling or manual turning of MSW compost and where mechanical processes such as compacting, crushing or shredding can create projectiles. The most critical control measures are safety glasses and puncture and slash resistant footwear and gloves.

Vehicular-use hazards include both operator hazards such as rollover and engulfment hazards and collision hazards with workers on the ground. Any vehicle that works on unsound or irregular surfaces should be equipped with rollover cages that will support the vehicle and allow the operator to survive. Pedestrian and vehicular traffic should be separated to the extent possible into distinct traffic areas, particularly where visibility is limited such as during open burning, at night and in composting yards where dense ground fogs may develop in cold weather.

Reports of increased atopic bronchopulmonary reactions such as asthma (Sigsgaard, Bach and Malmros 1990) and skin reactions can occur in waste workers, particularly where organic dust exposure levels are high.

Process-specific Hazards

Dispersion

Dispersion includes dumping waste into bodies of water, evaporation into the air or dumping with no effort at containment. Ocean dumping of MSW and hazardous wastes is rapidly declining. However, an estimated 30 to 50% of MSW is not collected in the cities of developing countries (Cointreau-Levine 1994) and is commonly burned or dumped in canals and streets, where it presents a significant public health threat.

Evaporation, sometimes with active heating at low temperatures, is used as a cost-saving alternative to incinerators or kilns, especially for volatile liquid organic contaminants such as solvents or fuel which are mixed with non-combustible wastes such as soil. Workers may face confined-space entry hazards and explosive atmospheres, especially in maintenance operations. Such operations should incorporate appropriate air emissions controls.

Storage/isolation

Isolation involves a combination of remote locations and physical containment in increasingly secure landfills. Typical sanitary landfills involve excavation with earth moving equipment, dumping of waste, compaction and daily cover with soil or compost to reduce pest infestations, odours and dispersion. Clay or impervious plastic caps and/or liners may be installed to limit water infiltration and leachate into groundwater. Test wells may be used to evaluate off-site leachate migration and to allow monitoring of leachate within the landfill. Workers include heavy equipment operators, truck drivers, spotters who may be responsible for rejecting hazardous waste and directing vehicle traffic flows and informal sector scavengers who may sort the waste and remove recyclables.

In areas dependent on coal or wood for fuel, ash can constitute a significant portion of the waste. Quenching prior to dumping, or segregation into ash monofills, may be necessary to avoid fires. Ash can cause skin irritation and caustic burns. Fly ash presents a variety of health hazards including respiratory and mucosal irritation as well as acute respiratory distress (Shrivastava et al. 1994). Low density fly ash can also constitute an engulfment hazard and can be unstable under heavy equipment and in excavations.

In many nations waste disposal continues to consist of simple dumping with open burning, which may be combined with informal scavenging of reusable or recyclable components with value. These informal sector workers face serious safety and health hazards. It is estimated that in Manila, Philippines, 7,000 scavengers work at the MSW dump, 8,000 in Jakarta and 10,000 in Mexico City (Cointreau-Levine 1994). Because of the difficulties in controlling work practices in informal work, an important step in controlling these hazards is to move separation of recyclables and reusables into the formal waste collection process. This may be performed by the waste generators, including consumers or household workers, by collection/sorting workers (e.g., in Mexico City collection workers officially spend 10% of their time sorting waste for sale of recyclables, and in Bangkok 40% (Beede and Bloom 1995)) or in pre-disposal waste separation operations (e.g., magnetic separation of metallic waste).

Open burning exposes workers to a potentially toxic mix of degradation products as discussed below. Because open burning can be used by informal scavengers to assist in separating metal and glass from combustible waste, it may be necessary to recover materials with salvage value prior to dumping in order to eliminate such open burning.

As hazardous wastes are successfully segregated from the waste stream, risks of MSW workers are reduced while quantities handled by hazardous waste site workers increase. Highly secure hazardous waste treatment and disposal sites depend on detailed manifesting of waste composition, high levels of worker PPE, and extensive worker training to control hazards. Secure landfills have unique hazards including slip and fall hazards where excavations are lined with plastic or polymer gels to reduce migration of leachate, potentially serious dermatological problems, heat stress related to work for extended periods in impermeable suits and supplied air quality control. Heavy equipment operators, labourers and technicians depend largely on PPE to minimize their exposures.

Oxidation (incineration and composting)

Open burning, incineration and waste-derived fuel are the most obvious examples of oxidation. Where the moisture content is low enough and the combustible content is high enough, increasing effort is made to utilize the fuel value in MSW either through the generation of waste-derived fuel as compressed briquettes or by incorporating electrical cogeneration or steam plants into municipal waste incinerators. Such operations can involve high levels of dry dusts due to efforts to produce a fuel with consistent heat value. Residual ash must still be disposed of, usually in landfills.

MSW incinerators involve a variety of safety hazards (Knop 1975). Swedish MSW incinerator workers showed increased ischemic heart disease (Gustavsson 1989), while a study of US incinerator workers in Philadelphia, Pennsylvania, failed to show a correlation between health outcomes and exposure groups (Bresnitz et al. 1992). Somewhat elevated blood lead levels have been identified in incinerator workers, primarily related to exposures to electrostatic precipitator ash (Malkin et al. 1992).

Ash exposures (e.g., crystalline silica, radioisotopes, heavy metals) can be significant not only in incinerator operations, but also at landfills and lightweight concrete plants where ash is used as aggregate. Although crystalline silica and heavy metal content vary with the fuel, this may present serious silicosis risk. Schilling (1988) observed lung function and respiratory symptom effects in ash exposed workers, but no changes observable by x ray.

Thermal degradation on pyrolysis products resulting from incomplete oxidation of many waste products can pose significant health risks. These products can include hydrogen chloride, phosgene, dioxins and dibenzofurans from chlorinated wastes, such as polyvinyl chloride (PVC) plastics and solvents. Non-halogenated wastes also can produce hazardous degradation products, including polyaromatic hydrocarbons, acrolein, cyanide from wools and silk, isocyanates from polyurethane and organotin compounds from a variety of plastics. These complex mixtures of degradation products can vary tremendously with waste composition, feed rates, temperature and available oxygen during combustion. While these degradation products are a significant concern in open burning, exposures in MSW incinerator workers appear to be relatively low (Angerer et al. 1992).

In MSW and hazardous waste incinerators and rotary kilns, control of combustion parameters and the residence time for waste vapours and solids at high temperatures is critical in destruction of wastes while minimizing the generation of more hazardous degradation products. Workers are involved in incinerator operation, loading and waste transfer into the incinerator, waste delivery and unloading from trucks, equipment maintenance, housekeeping and ash and slag removal. While incinerator design can limit necessary manual labour and worker exposures, with less capital-intensive designs there may be significant worker exposures and a need for regular confined space entry (e.g., chipping for removal of slag from glass waste from incinerator grates).

Composting

In aerobic biological processes the temperature and speed of oxidation are lower than incineration, but it is nevertheless oxidation. Composting of agricultural and yard wastes, sewage sludge, MSW and food wastes is increasingly common in city-scale operations. Rapidly developing technologies for biological remediation of hazardous and industrial wastes often involve a sequence of aerobic and anaerobic digestion processes.

Composting usually occurs either in wind rows (long piles) or in large vessels which provide aeration and mixing. The objective of composting operations is to create a mix of waste with optimum ratios of carbon and nitrogen (30:1) and then maintain moisture at 40 to 60% by weight, greater than 5% oxygen and temperature levels 32 to 60oC so that aerobic bacteria and other organisms can grow (Cobb and Rosenfield 1991). Following separation of recyclables and hazardous wastes (which typically involves hand sorting), MSW is shredded to create more surface area for biological action. Shredding can produce high noise and dust levels and significant mechanical guarding concerns. Some operations use ganged hammer-mills to allow reduced front-end sorting.

In-vessel or drum composting operations are capital intensive but allow more effective odour and process control. Confined space entry is a significant hazard for maintenance workers as high levels of CO2 may be released causing oxygen deficiency. Lockout of equipment prior to maintenance is also critical as mechanisms include internal screw-drives and conveyors.

In less capital intensive wind row composting operations, waste is shredded and placed in long piles which are mechanically aerated through perforated pipes or simply by turning, either with front-end loaders or manually. Wind rows may be covered or roofed to facilitate maintenance of constant moisture content. Where specialized wind row turning equipment is used, chain mixing-flails rotate at high speed through the compost and should be well guarded from human contact. As these flails rotate through the wind row, they eject objects which can become dangerous projectiles. Operators must assure safe clearance distances around and behind the equipment.

Regular temperature measurements with probes allow monitoring the progress of composting and assure high enough temperatures to kill pathogens while allowing adequate survival of beneficial organisms. At moisture contents of 20 to 45% when the temperature exceeds 93oC there can also be a spontaneous combustion fire hazard (much like a silo fire). This is most likely to occur when piles exceed 4 m in height. Fires can be avoided by keeping pile heights below 3 m, and turning when the temperature exceeds 60°C. Facilities should provide water hydrants and adequate access between wind rows for control of fires.

Hazards in composting operations include vehicle and mechanical hazards resulting from tractors and trucks involved in turning wind-rows of waste to maintain aeration and moisture content. In cooler climates the elevated temperatures of compost can produce dense ground fogs in a work area occupied by heavy equipment operators and pedestrian workers. Compost workers report more nausea, headache and diarrhoea than their counterparts in a drinking water plant (Lundholm and Rylander 1980). Odour problems can occur as a result of poor control of the moisture and air required for the composting to progress. If anaerobic conditions are allowed to occur, hydrogen sulphide, amines and other odorous materials are generated. In addition to typical disposal worker concerns, composting involving actively growing organisms can raise MSW temperatures high enough to kill pathogens, but can also produce exposures to moulds and fungi and their spores and toxins, especially in compost bagging operations and where compost is allowed to dry. Several studies have evaluated airborne fungi, bacteria, endotoxins and other contaminants (Belin 1985; Clark, Rylander and Larsson 1983; Heida, Bartman and van der Zee 1975; Lacey et al. 1990; Millner et al. 1994; van der Werf 1996; Weber et al. 1993) in composting operations. There is some indication of increased respiratory disorders and hypersensitivity reactions in compost workers (Brown et al. 1995; Sigsgaard et al. 1994). Certainly bacterial and fungal respiratory infections (Kramer, Kurup and Fink 1989) are a concern for immune-suppressed workers such as those with AIDS and those receiving cancer chemotherapy.

Reduction (hydrogenation and anaerobic digestion)

Anaerobic digestion for sewage and agricultural waste involves closed tanks, often with rotating brush contacts if nutrients are dilute, which can pose serious confined space entry concerns for maintenance workers. Anaerobic digesters are also commonly used in many countries as methane generators which may be fuelled with agricultural, sanitary or food wastes. Methane collection from MSW landfills and burning or compression for use is now required in many countries when methane generation exceeds specified thresholds, but most landfills have inadequate moisture for anaerobic digestion to proceed efficiently. Hydrogen sulphide generation is also a common result of anaerobic digestion and can cause eye irritation and olfactory fatigue at low levels.

More recently, high temperature reduction/hydrogenation has become a treatment option for organic chemical wastes. This can involve smaller, and therefore potentially mobile, installations with less energy input than a high temperature incinerator because metallic catalysts allow hydrogenation to proceed at lower temperatures. Organic wastes can be converted into methane and used as fuel to continue the process. Critical worker safety concerns include explosive atmospheres and confined space entry for cleaning, sludge removal and maintenance, hazards of transporting and loading the liquid feed wastes and spill response.

Summary

As wastes are viewed as resources for recycling and reuse, waste processing increases, resulting in rapid change in the waste disposal industry globally. Occupational health and safety risks of waste disposal operations often go beyond obvious safety hazards to a variety of chronic and acute health concerns. These hazards are often faced with minimal PPE and inadequate sanitary and wash-up facilities. Industrial waste reduction and pollution prevention efforts are increasingly shifting recycling and reuse processes away from contracted or external waste disposal operations and into production work areas.

Top priorities in controlling occupational safety and health hazards in this rapidly changing industry sector should include:

  • integrating informal sector work into the formal work process
  • providing adequate toilet and wash-up facilities and safe drinking water
  • eliminating open burning and waste dispersion into the environment
  • segregating waste streams to facilitate characterization of wastes and identification of appropriate control measures and work practices
  • minimizing mixed vehicular and pedestrian traffic in work areas
  • following appropriate excavation practices for soil and waste characteristics
  • anticipating and controlling hazards prior to entry into confined spaces
  • minimizing respirable dust exposures in high dust operations
  • using safety glasses and slash and puncture resistant shoes and gloves
  • integrating occupational safety and health concerns when introducing process change plans, particularly during transitions from open dumping and landfills to more complex and potentially more hazardous enclosed operations such as composting, mechanical or manual separation for recycling, waste to energy operations or incinerators.

 

In this period of rapid change in the industry, significant improvements in worker health and safety can be made at low cost.

 

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Monday, 28 March 2011 20:06

Wood Handling

Wood may arrive at a pulp mill woodyard in the form of raw logs or as chips from a lumber mill. Some pulp mill operations have on-site sawmills (often called “woodrooms”) which produce both marketable lumber and stock for the pulp mill. Sawmilling is discussed in detail in the chapter Lumber. This article discusses those elements of wood preparation which are specific to pulp mill operations.

The wood preparation area of a pulp mill has several basic functions: to receive and meter the wood supply to the pulping process at the rate demanded by the mill; to prepare the wood so that it meets the mill’s feed specifications for species, cleanliness and dimensions; and to collect any material rejected by the previous operations and send it to final disposal. Wood is converted into chips or logs suitable for pulping in a series of steps which may include debarking, sawing, chipping and screening.

Logs are debarked because bark contains little fibre, has a high extractives content, is dark, and often carries large quantities of grit. Debarking can be done hydraulically with high-pressure water jets, or mechanically by rubbing logs against each other or with metal cutting tools. Hydraulic debarkers may be used in coastal areas; however, the effluent generated is difficult to treat and contributes to water pollution.

Debarked logs may be sawn into short lengths (1 to 6 metres) for stone groundwood pulping or chipped for refiner mechanical or chemical pulping methods. Chippers tend to produce chips with a considerable size range, but pulping requires chips of very specific dimensions to ensure constant flow through refiners and uniform cooking in digesters. Chips are therefore passed over a series of screens whose function is to separate chips on the basis of length or thickness. Oversized chips are rechipped, while undersized chips are either used as waste fuel or are metered back into the chip flow.

The requirements of the particular pulping process and chip conditions will dictate the duration of chip storage (figure 1; note the different types of chips available for pulping). Depending on fibre supply and mill demand, a mill will maintain a 2 to 6 week unscreened chip inventory, usually in large outdoor chip piles. Chips may degrade through auto-oxidation and hydrolysis reactions or fungal attack of the wood components. In order to avoid contamination, short-term inventories (hours to days) of screened chips are stored in chip silos or bins. Chips for sulphite pulping may be stored outside for several months to allow volatilization of extractives which may cause problems in subsequent operations. Chips used in kraft mills where turpentine and tall oil are recovered as commercial products typically proceed directly to pulping.

Figure 1. Chip storage area with front end loaders

PPI030F1

George Astrakianakis

 

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