Journal of Environmental Protection
Vol. 3  No. 5 (2012) , Article ID: 19535 , 23 pages DOI:10.4236/jep.2012.35054

Disposal and Treatment Methods for Pesticide Containing Wastewaters: Critical Review and Comparative Analysis

Mariam T. Al Hattab, Abdel E. Ghaly

Department of Process Engineering and Applied Sciences, Faculty of Engineering, Dalhousie University, Halifax, Canada.

Email: abdel.ghaly@dal.ca

Received February 27th, 2012; revised March 28th, 2012; accepted April 27th, 2012

Keywords: Pesticides; Health; Soil; Water; Disposal; Treatment; Land Cultivation; Disposal Pits; Evaporation Ponds; Landfills; Incineration; O3/UV; Fenton Oxidation; Hydrolysis; Bioremediation; Bioaugmentaion

ABSTRACT

Pesticides provide the primary means for controlling organisms that compete with man for food and fibre or cause injury to man, livestock and crops. They played a vital role in the economic production of wide ranges of vegetable, fruit, cereal, forage, fibre and oil crops which now constitute a large part of successful agricultural industry in many countries. After application to the target areas, pesticide residues are removed from applicators by rinsing with water which results in the formation of a toxic wastewater that represents a disposal problem for many farmers. Pesticides can adversely affect people, pets, livestock and wildlife in addition to the pests they are intended to destroy. The phenomenon of biomagnification of some pesticides has resulted in reproductive failure of some fish species and egg shell thinning of birds such as peregrine falcons, sparrow hawk and eagle owls. Pesticide toxicity to humans include skin and eye irritation and skin cancer. Therefore, care must be exercised in the application, disposal and treatment of pesticides. Currently, disposal of pesticide wastewater is carried out by: 1) land cultivation, 2) dumping in soil pits, plastic pits and concrete pits or on land and in extreme cases in streams near the rinsing operation, 3) use of evaporation beds and 4) land filling. These methods of disposal are unsafe as the surface run off will reach streams, rivers and lakes and the infiltration of the wastewater into the local soil will eventually reach ground water. The treatment methods currently used for pesticide wastewater include: 1) incineration (incinerators and open burning), 2) chemical treatments (O3/UV, hydrolysis, Fenton oxidation and KPEG), 3) physical treatments (inorganic, organic absorbents and activated carbon) and 4) biological treatments (composting, bioaugmentation and phytoremediation). Therefore, the choice of safe, on farm disposal techniques for agricultural pesticides is very important. A comparative analysis was performed on 18 methods of pesticide disposal/treatment using six criteria: containment, detoxification ability, cost, time, suitability for on farm use, size and evaporation efficiency. The results indicated that of the 18 methods evaluated, 9 scored above 80/100 and can be used on farm. They were organic absorbents (97), composting (94), bioaugmentation (92), inorganic absorbents (90), Fenton oxidation (86), O3/UV (83), activated carbon (82), hydrolysis (82), and land cultivation (80). The other methods are not suitable for on farm use as they suffered from containment problems, high cost and variability of effectiveness.

1. Introduction

Pesticides provide the primary means for controlling organisms that compete with man for food and fibre or cause injury to man, livestock and crops. They are classified based on the pest they control as shown in Table 1. Pesticide expenditures account for 13% - 22% of total costs of production per hector. The worldwide pesticide consumption and expenditures in 2007 (Table 2) were 2.37 billion kg and 39.4 billion dollars, respectively [1]. Table 3 illustrates the top 10 countries applying higher rates (kg/hectare) of pesticides [2]. Ten companies (Table 4) account for 87.2% of the total sales [3].

Pesticides played a vital role in the economic production of wide ranges of vegetable, fruit, cereal, forage, fibre and oil crops which now constitute a large part of successful agricultural industry in many countries. They lower crop losses, increase revenue to farmers from the additional marketable yield obtained with their use and thus lower the cost of production per unit output [4]. Other benefits include: 1) reduced uncertainty of crop loss from pests, 2) increased profit to farm input suppliers (machinery, fertilizer, chemicals and seed companies) from increased sale, 3) benefit to consumers through decreased price of raw foods or improved quality of food products and 4) benefit to society as whole (farmers, consumers, farm suppliers, food processors) from increased employment opportunities and expanded export

Table 1. Common types of pesticides.

Table 2. 2007 worldwide consumption and expenditures of pesticide active ingredients [1].

Table 3. Top 10 countries applying pesticide at higher rates in 2000 [2].

Table 4. Top 10 pesticide companies in 2007 [3].

of food products [5,6]. The benefit/cost ratio vary from 4 to 33 (for every dollar spent on pesticide farmers receive an additional $4 - 33 in revenue) depending upon crop rotation and year [4,7].

After pesticides are applied to the target areas, pesticide residues remain in containers and application equipment. These residues are removed from applicators by rinsing with water which results in the formation of a toxic wastewater that can adversely affect people, pets, livestockand wildlife [8-10]. The resulting ecological impact of unsafe disposal of pesticides can be severe depending on the type of pesticide and the amount contained in the wastewater. The phenomenon of biomagnification of some pesticides has resulted in reproductive failure of some fish species [11,12] and egg shell thinning of birds such as peregrine falcons, sparrow hawk and eagle owls [13]. Pesticide toxicity to humans include skin and eye irritation and skin cancer [14]. Therefore, care must be exercised in the application, disposal and treatment of pesticides. Currently, disposal of pesticide wastewater is carried out by several methods including: 1) land cultivation, 2) dumping in soil pits, in ditches, in lagoons, on land, and in extreme cases in sewers and streams near the rinsing operation, 3) use of evaporation pond and 4) land filling. These methods of disposal are totally unsafe. The surface run off will reach streams, rivers and lakes and the infiltration of the wastewater into the local soil will eventually end up in the ground water. The treatment methods currently used for pesticide containing wastewater include: 1) incineration, 2) chemical treatment, 3) physical treatment and 4) biological treatment. These treatment methods either require land or are expensive and suffer from variability of effectiveness [15]. Thus, the development and selection of safe, on farm disposal/treatment technique for agricultural pesticides is paramount.

The aim of this study was to review the current methods of disposal and treatment of pesticides and to perform a comparative analysis to determine the most appropriate method for on farm use.

2. Pesticide Disposal Methods

The methods for the disposal of low level pesticides (Table 5) include: land cultivation, disposal pits, evaporation ponds and landfills [16-20]. There are three types of disposal pits: soil pit, plastic pit and concrete pit.

2.1. Land Cultivation

In this method, excavated contaminated soil is spread out in a thin layer on uncontaminated soil (Figure 1) in order to allow for natural chemical and biological processes to transform and degrade the contaminants. Soil contains microbes (fungi, algae and bacteria) capable of

Table 5. Disposal methods of pesticide containing wastewater.

Figure 1. Land cultivation of contaminated soil [21].

metabolizing pesticides [22,23]. The ability of bacteria to metabolize pesticides has been well documented by several researchers. Bhadhade et al. [24] reported that soil bacteria was capable of degrading 83% - 93% of the organo-phosphorouspesticide monocrotophos. Ohshiro et al. [25] reported a 96% reduction in isoxathion from the organophosphouruspestiside by bacteria isolated from turf green soil. Kearney et al. [26] reported that soil microbes were capable of degrading 90% of the alachlor pesticide within 30 - 40 days. Tang and You [27] reported that the triazophos bacteria was capable of degrading 33.1% - 95.8% of pesticides in soil.

Racke and Coats [28] reported that after soil has been treated with a pesticide a few times its microorganisms build up a need for that pesticide which results in fairly rapid degradation of any additional applications. Schoen and Winterlin [29] stated that natural soil degradation is effective when low concentrations of the pesticide are present, but with high concentrations of pesticide it becomes much more difficult to degrade. Felsot [30] stated that land cultivation is only effective for compounds that can be biotransofrmed or biominerlized by soil microbes. Somasundaram et al. [31] reported that the ability of soil microbes to degrade certain pesticides is affected by pesticide toxicity to soil microbes that are responsible for the degradation. Felsot et al. [22] stated that land cultivation is effective if the pesticide is degraded at the same or faster rate than it is applied to the field. Felsot et al. [32] noted that land cultivation can be enhanced by the addition of organic amendments such as sewage sludge.

2.2. Soil Pit

A primary method for disposing of liquid pesticide waste is by dumping it in an unlined soil evaporation pit (Figure 2), usually 15 × 15 × 1 m [33]. Schoen and Winterlin [29] reported that factors such as chemical structure and concentration of pesticide play a major role in the degradation of pesticides in soil pits. Gan and Koskinen [34] stated that the dissipation of the pesticide decreases as the concentrations of pesticide increases. Dzantor and Felsot [35] and Gan et al. [36] noted that high pesticide concentrations may cause microbial toxicity which would inhibit the degradation of the pesticide.

Several researchers [22,34,36,37] noted that the prolonged dissipation of pesticides opens a window for runoff and leaching, especially at higher pesticide concentrations. Gan et al. [36] reported that 50% dissipation of the alachlor pesticide in soil, at concentrations of 4 and 4 300 mg/kg took approximately 2 and 52 weeks, respectively. Gan et al. [38] noted that atrazine pesticide took approximately 4 and 24 weeks to be dissipated to half the concentration of 7 and 6400 mg/kg in soil, respectively. Schoen and Winterlin [29] noted that captan, trifluralin and diazinon at concentrations of 100 mg/kg took 1 - 2, 116 - 189 and 77 - 160 weeks to dissipate to half the concentration while captan, trifluralin and diazinon at concentrations of 1000 mg/kg took 30 - 48, 168 - 544 and 77 - 160 weeks to reach 50% disappearance in soil, respectively.

2.3. Plastic Lined Pit

This method for disposal of pesticide waste requires proper selection of the site to avoid leaching and runoff.

Figure 2. A soil pit for disposal of pesticide water [33].

The site should be in an area where there is no danger of contaminating dwellings groundwater sources and surface water used for crop and livestock production. The pit should be on a levelled ground with a depth of 0.5 - 1 m covered with a plastic liner and a layer of soil is laid on top of the liner (Figure 3). The pit should be open to the atmosphere in order to allow for water evaporation into the atmosphere. A roof cover will prevent the water level from raising due to rain or snow. The wastewater is pumped into the pit for pesticide biodegradation by soil microbes [22]. Hall et al. [20] reported that the presence of microbes in the soil water mixture in plastic lined pits was responsible for the degradation of pesticide and no accumulation of pesticide was noted in the pits. Junk and Richard [39] evaluated the effectiveness of 90,000 L polyethylene lined disposal pit with over 150 kg of 25 different types of pesticides for over 2 years and concluded that this method was in fact effective for disposal of pesticide waste with insignificant release to air and water surroundings.

Figure 4 illustrates a cross section view of a simple small scale plastic pit used to dispose of pesticide waste. It consists of a plastic drum with a length and width of 75 × 55 cm, respectively. Inside the drum is a mixture of 15 kg of soil and 60 L of water, that was used to treat pesticide waste which was introduced into the system through the inlet. Junk et al. [19] used 56 plastic containers filled with 15 kg of soil and 60 L of water to test the degradation of alachlor, atrazine, triflualin, 2,4-D ester, carbaryl and parathion and found this system not suitable for atrazine but was effective and very rapid for 2,4-D and carbayl. They concluded that: 1) the plastic container

Figure 3. A plastic lined evaporation pit for disposal of pesticide wastewater [16].

Figure 4. A cross section of a plastic pit for disposal of pesticide wastewater [40].

provided satisfactory containment for most common pesticides, 2) soil was a satisfactory source for microorganisms, 3) aeration and buffers had questionable value, 4) half life concept for degradation was not applicable and 5) sampling from small disposal sites was a problem.

2.4. Concrete Pit

Similar to the plastic lined pit, the concrete pit should be on levelled ground with a depth of 0.5 to 1 m, a length of 8 - 10 m and a width of 3.5 m and reinforced with 0.20 m thick concrete walls. The pit consists of a top and bottom layer of gravel that is 4 cm in diameter with the middle layer consisting of topsoil (Figure 5). The pit should also have a cover to prevent rise in water level from rain or snow but remain open to the atmosphere in order to allow for water evaporation.

Johnson and Hartman [41] tested the microbiological activity in a concrete pit and concluded that the degradation process in the pit was effective and no long-term accumulation of pesticide was present. Junk and Richard [39] tested the effectiveness of 30,000 L concrete disposal pit with over 50 kg of 40 different types of pesticides for 8 years and concluded that this method was in fact effective for disposal of pesticide waste with insignificant release to air and water surroundings. Hall [42] tested the effectiveness of an open concrete disposal pit for the degradation of 45 pesticides over five months and concluded that the biodegradation of the pesticides was successfully accomplished and the pit did not leak or pollute the air, but the system was too large and complicated for most farms.

2.5. Evaporation Beds

Lined evaporation beds (Figure 6) are used for the disposal of pesticide wastewater. Leach lines underneath the soil surface supply the beds with the pesticide residues from washing equipment. The pesticides rise to the beds surface where they are degraded through photochemical, chemical and biological actions and are distributed via air vapour. Some of the beds have hydrated lime incurporated into the soil in order to aid in the degradation of certain pesticides. A medium scale disposal system of this type costs up to $50,000 to construct [16,22].

Hodapp and Winterlin [44] reported a reduction in the diazinon pesticide of 62.54% using lined evaporation bed without lime and a degradation of 77.75% with lime. They also reported an ethyl parathion reduction of 69.83% using lime treatment in the beds and a reduction of 45.45% without the use of lime. Winterlin et al. [16] tested ten (6 × 12 × 1 m) lined (with a butyl rubbermembrane liner and 36 cm of sandy loam soil) evaporation beds to determine their pesticide decay effectiveness. Pesticide rainsate was introduced through subsurface tiles in limited amounts and the effects of geography, climate and lime application were examined. The method appeared to be beneficial for disposal of some pesticides but not all. Over 100 pesticides were tested, but only 46 were actually detected.

This method for the disposal of pesticide containing wastewaters is advantageous because the beds are economical, little maintenance is required, do not build up high levels of pesticides and are effective in degrading as well as containing the pesticides without excessive exposure through air vapour [16,44]. It is considered an economical, on-site method of disposal which requires only annual monitoring. The disadvantages appear to be the development of a high concentration of residue in the top layer of the soil and the difficulty in acquiring a representative sample [33].

2.6. Land Filling

Landfills are sites that dispose of waste by burial into the soil where microorganisms are used to change the composition of the toxic elements. Landfills for pesticides (Figure 7) are equipped with drying pits (Figure 8) containing soil to provide the microbes needed to break down the pesticide components into non harmful elements. A nearby sump for the propose of draining and rinsing the containers that have not been fully emptied or rinsed [47,48].

Munnecke [49] reported that soil bacteria were capable of hydrolyzing ethyl parathion found in pesticide container residues within 16 h. Johnson and Lavy [50] reported that carbofuran, thiobencarb and triclopyr buried in degrading containers dissipated to 50% of the initial concentration with the first 94 days or less, while benomyl took 179 - 1020 d before 50% dissipation. They also noted that the rates of dissipation decreased with an increase in soil depth.

Yasuhara et al. [51] detected 190 compounds in landfill leachates in Japan. Williams et al. [52] reported that the pesticide mecoprop is found in landfill leachate because it is resistant to anaerobic degradation. Christensen et al. [53] noted the presence of the pesticide bentazon, N,N-Diethyltoluamide and mecoprop in landfill leachate because of their persistence to anaerobic landfill conditions. Alloway and Ayres [54] noted the presence of the pesticides atrazine and simazine in landfill leachate.

3. Pesticide Treatment Methods

The pesticides treatment methods (Table 6) include: 1) thermal treatment, 2) chemical treatments, 3) physical

Figure 5. A cross section of concrete pit for disposal of pesticide wastewater [20].

Figure 6. Evaporation beds for disposal of pesticide wastewater [43].

Figure 7. A landfill for disposal of pesticide wastes [45].

Figure 8. The landfill leachate collection pit [46].

treatments and 4) biological treatments. Thermal treatments include incineration and open burning. Chemical treatments include ozonation/UV radiation, Fentonoxidation, hydrolysis and KPEG. Physical treatments are based on absorption using activated carbon, inorganic and organic materials. Biological treatments include composting, phytoremediation and bioaugmentation.

3.1. Incineration

Pesticide Incineration is a high temperature oxidation process where the pesticide is converted into inorganic gases (water vapour, CO2, volatile acids, particles and metal oxides) and ash [22,54]. Incineration of pesticide should be operated at temperatures higher than 1000˚C so that the pesticide can be treated within the first 2 seconds. At such temperatures, smoke production is nil and the generated combustion gases are similar to those generated by wood burning [22]. Temperatures lower than 1000˚C can also be used as long as the incineration time of the pesticide does not exceed 2 seconds [23]. However, lower temperatures tend to produce toxic intermediate products [56].

Kennedy et al. [57] noted change in the combustion efficiency over the temperature range of 600˚C - 1000˚C. Ferguson and Wilkinson [55] reported that incineration has 99.99% destruction efficiency at temperatures of 1000˚C and a retention time of 2 s in the combustion zone. Steverson [58] reported a 99% destruction efficiency for 16 currently used insecticides and herbicides at temperatures ranging from 200˚C to 700˚C. Linak et al. [59] reported an incineration efficiency of greater than 99.99% for dinoseb. Ahling and Wiberger [60] noted that the incineration of fenitrothion and malathion at temperatures lower than 600˚C gave emissions of 1% - 2% of the pesticide amount added and temperatures above 700˚C would be required to achieve safe destruction and emission levels.

Table 6. Current treatment methods of pesticide containing wastewater.

Incinerators (Figure 9) capable of achieving high levels of destruction are equipped with a combustion chamber, an afterburner, scrubbers and electrostatic filters. Ferguson and Wilkinson [55] reported the following performance standards for incinerating hazardous wastes: 1) the incinerator must achieve a destruction and removal efficiency greater than 99.99% for each of the chemicals present in the waste feed, 2) HCl emissions must not exceed 1.8 kg/h or 1% of the HCl in the stack gas prior to entering any pollution control equipment and 3) the particulate matter emitted must not exceed 180 mg/DSCM when corrected to 7.0% O2. The advantages of incineration include: 1) effectiveness in degrading chlorinated organics, 2) destruction efficiency of 99.99% and 3) setup at locations next to plants generating the waste. The disadvantages of incineration technology include: 1) need for sophisticated equipment 2) production of cyanide in the off gas during the incineration of organonitrogen pesticides, 3) too costly and complex, 4) it is intended for centralized large scale disposal and 5) not recommended for inorganic pesticides [22].

3.2. Open Burning

This method combusts pesticides and pesticide waste containers by piling up empty paper and plastic containers and setting them on fire (Figure 10). Although this method is inexpensive and convenient, it is hazardous to workers, plants and animals. It is prohibited in some cases by the Regional Air Quality regulations in the US [1]. It emits gases, smoke and fumes into the atmosphere as well as toxic residues that are left in the containers.

Adebona et al. [63] noted several products of incomeplete combustion, polyaromatic hydrocarbons and low levels of dioxins in open burning tests on 22.7 kg insecticide bags. Oberacker et al. [64] noted that after burning bags containing phorate, 2% of the phorate was released into the air and 0.5% remained in the solid residues. Felsot et al. [22] reported that bags containing atrazine released 13% of the remaining product into the air while 25% remained as residue. Such results indicate that the temperatures for complete combustion were not reached or were not maintained long enough in order to obtain destruction efficiencies of 99.99% or greater [22].

3.3. Ozonation/UV Radiation

The use of ozone and UV radiation to enhance the oxidation of aromatic compounds was investigated by several researchers [17,28,65]. Ozonation is more effective treatment method in the presence of UV light because it canform hydrogen radicals which are very effective oxidizing agents [66,67]. The benefits of this process are its mobility, ease of operation and rapid effects. The disadvantages are its high energy consumption and initial equipment cost [18].

Kuo [68] used a UV/ozonation system (Figure 11) consisting of a medium-pressure mercury vapor lamp with a water cooling jacket and an ozone generator. The lamp power consumption was 150 W and was capable of 14.3 W output (at 3.0 mW/cm2 at a distance of 9 cm). The O3 was pumped at a rate of 400 mg O3/hr/L solution. A solution of 2% KI was used for absorbing the residual ozone from the reactor.

Figure 9. An incinerator for pesticide wastes [61].

Figure 10. Open burning of pesticide wastes [62].

Somlich et al. [17] noted that irradiation of the alachlor pesticide achieved de-chlorination of the compound, while ozonation works to oxidize the compound into several intermediate products. Under Ultraviolet irradiation, the photon absorption by the carbonyl present in the compound is then followed by the loss of the chlorine. The pesticide degradation reactions that take place under UV/ozonation are as follow [69]:

(1)

(2)

Kearney et al. [18] monitored the degradation of alachlor using a UV/O3 system by measuring the concentration of the 14 CO2 released. Under UV radiation, the alachlor pesticide was completely depleted from the water with the presence of oxygen within 25 minutes while it and took 50 minutes before it was fully depleted with ozone alone.

3.4. Fenton Oxidation

The Fenton process can be used as part of an oxidative system (Figure 12) to treat and degrade pesticides. It consists of hydrogen peroxide (H2O2) and iron salts at low pHs [71]. The iron salts act as a catalyst, increasing the effectiveness of the H2O2 by forming highly reductive hydroxyl radicals. The radicals are capable of oxidizing other species that are present in the solution as follows [72].

(3)

(4)

Hydroxyl radicals are very powerful oxidizing agents with a 2.33 V oxidative potential [72]. The rate of degradation of organic pollutants is strongly accelerated by UV irradiation. The photolysis of the Fe3+ complexes allows the regeneration of Fe2+ thus allowing the reaction to proceed much quicker in the presence of H2O2 [73]. The advantages of this method for pesticide treatment are: low cost, ease of operation, simplicity and the wide range of temperature that can be used [72].

Fallmann et al. [70] noted a 72% reduction in 100 ppm

Figure 11. A UV/O3 system for the treatment of pesticide wastewater [68].

Figure 12. A photo assisted Fenton system for treatment of pesticide wastewater [70].

total organic carbon solution using 23 mL of hydrogen peroxide and a reaction time of 124 minutes in a photo assisted Fenton process. Larson et al. [74] reported that in the presence of ferric perchlorate and a mercury lamp, the atrazine pesticide had a half-life of less than 2 minutes compared to 1500 minutes when iron salt was not present. Huston and Pignatello [75] noted a half-life of less than 10 minutes for the captanpesticide using UV assisted Fenton reagent at a pH of 2.8. Pignatello and Sun [76] reported a half-life of 2 minutes for methyl parathion using UV assisted Fenton reagent. Doong and Chang [77] reported a half-life of less than 10 minutes for alachlor pesticide under photo assisted Fenton reagent at a pH of 2.8.

3.5. Hydrolysis

This method for pesticide treatment works by hydrolyzing the ester linkages found in pesticide compounds, including pyrethroids, carbamates, organophosphates and acetaniledes. These compounds can be hydrolyzed in solutions with high pH levels [22]. Desmarchelier [78] used calcium hydroxide for ester hydrolysis and found it to be a safer alternative to sodium and potassium hyoxides for the hydrolysis of fenitrothion pesticide. Lee et al. [79] noted that under basic conditions, sodium perborate was more effective in the hydrolysis of organophosorus than sodium hydroxide, because the peroxide anion released from sodium perborate is much more reactive to organophosphorus than the hydroxyl ion. Qian et al. [80] noted an enhancement in the hydrolysis process of mevinphos, diazinon, methyl parathion, malathion and parathion in lake water (10 mg/L) using sodium perborate at pH of 9.88. However, with the presence of soil, the reaction was noted to be significantly slower and the concentration of perborate had to be increased by four folds.

Metal oxide and divalent metal ions have been noted for their ability to catalyze the hydrolysis of organphosorus insecticides. Smolen and Stone [81] reported that the phophorothionate insecticides (chlorpyrifos-methyl, zinophos, diazinon, parathion-methyl and runnel) and phosphorooxonates (chlorpyrifos-methyl oxon and paraoxon) were most effectively catalyzed by Copper (II). The downside of catalysis using metal oxides is the formation of products with significant toxicity [22]. Badawi and Ahmed [82] noted that the hydrolysis of the pesticides diazinon, cypermethrin and carbaryl (Figure 13) was effective and accelerated by the addition of a copper (II) ion complex.

Figure 13. Hydrolysis of cypermethrin, carbaryl and diazinon pesticides [82].

3.6. KPEG

Potassium polyethylene glycol ether (KPEG) is capable of destroying chlorinated pesticides. Chlorinated hydrocarbons and cyclodienes are resistant to degradation by hydrolysis. Dechlorinating these pesticides with KPEG would then enable their biodegradation through land treatment processes. KPEG was found to be capable in dechlorinating polychlorinated biphenyls (PCBs) in soil and solvents [83,84]. In older formulations of phenoxy herbicide, KPEG was found to be capable of degrading dioxins and dibenzofurans [85]. The reaction that takes place consists of a nucleophilic substitution and a phase transfer at the carbon-halogen bond as illustrated by the following equations [22].

(5)

(6)

(7)

where:

PEG = polyethylene glycol monomethyl ether Ar = aromatic nucleus Taylor et al. [86] reported that the vessel for the KPEG reaction consists of a 55-gal drum (surrounded with heat tape capable of maintaining the temperature at 70˚C - 85˚C) and an electric motor with a mixer (Figure 14). With the reagents KOH and PEG, this vessel was capable of degrading 98% of phenoxy herbicide waste. The generated waste contained in the drums can remain there, eliminating the need for transfer into another container. Vapor emitted from the reaction drums are condensed in a water drum, the remaining condensables are traped in the scrubber containing sodium hypochlorite solution. Vapors are then passed through an activated carbon absorbent and as well as a molecular sieve [86].

The materials and chemicals needed for the KPEG process are easy to find [22]. The disadvantage of the KPEG process are 1) high clay content, acidity and high natural organic matter interferes with KPEG reaction and 2) its not recommended for large waste volumes with concentrations above 5% for chlorinated contaminants. If necessary, emissions can be controlled by construction of a vent system with scrubber and absorbent.

3.7. Inorganic Absorbents

Pesticide adsorption can be performed using anionic clays (layered double hydroxides) which are simple to prepare [87], hydrotalcite, which occurs in nature may also be used as a layered double hydroxide (LDH). A variety of compounds can be formed by changing the cation metal. In order for a material to be considered as a good adsorbent it must possess the following properties: 1) a granular structure, 2) insoluble in water, 3) chemical stability and 4) have a high mechanical strength [88]. Figure 15 is multi-functional gravity filter which can be used for various water treatment methods by employing various adsorbent media [89].

Niwas et al. [90] reported that styrene supported zirconium (IV) tungstoophosphates was successful in adsorbing the pesticide phosphamidan. Inacio et al. [86] noted that the inorganic adsorbent Mg3AlCl was capable of adsorbing the MCPA herbicide within 30 - 45 minutes at room temperature. Boussahel et al. [91] noted a removal efficiency in ayanaz in and atrazine of 85% - 90% using CaCl2 or CaSO4. Bojemueller et al. [92] reported that the pesticide metolachlor can be adsorbed by bentonites and the adsorption efficiency can be doubled by increasing the temperature. Li et al. [93] noted that the pesticide glyphosate was adsorbed on the external surface of MgAl-LDH at low concentrations, while at high glyphosate concentrations an inter layer ion exchange occurred.

3.8. Organic Absorbents

Various organic materials can be used as good adsorbents for pesticide removal. Ahmaruzzaman and Gupta [88] reported that rice husk is insoluble in water, possesses an

Figure 14. A KPEG process with vent system [86].

Figure 15. Filters used to treat pesticide wastewater through adsorption [89].

irregular granular structure and has a high mechanical strength and chemical stability that make it a good adsorbent. Chowdhury et al. [94] noted that treated rice husk was capable of removing 89% - 97% of malachite green pesticide. Akhtar et al. [95] investigated the adsorption potential of selected agricultural waste materials (rice, barn, bagasse fly ash from sugarcane and rice husk) for the pesticide removal of methyl parathion from wastewater and reported pesticide removal efficiencies in the range of 70% - 90% within 90 minutes. Memon et al. [96] reported that thermally treated watermelon peels were capable of removing 99% of the methyl parathion pesticide. Al hattab and Ghaly [97] reported a captan removal efficiency of 99.2% and 98.5% using hay and soybean plant residues, respectively.

3.9. Activated Carbon

Carbon adsorption treatment method for pesticide containing wastewater is used in the pesticide manufacturing industry as well as in pesticide cleanup [98,99]. The activated carbon system consists of a prefilter made up of sand or an alum flocculation chamber with a carbon filter [100-102]. Dennis and Kobylinski [100] reported on a Carbolator (Figure 16) system which uses a suspended bed of carbon packed in bags of floating porous polyethylene in order to avoid clogging. The water was continuously recirculated through the carbon filters by directing it back into the waste holding tank.

Felsot et al. [22] reported that rinsewater containing malathion, propoxur, chlorpyifos, diaxinon and dimethoate were all removed to nondetectable levels using the Carbolator. This process reduced the amount of waste generated by several magnitudes through efficiently absorbing pesticides form the water. Kobylinski et al. [99] used a Carbulator 35B to remove baygon, dimethoate, diazinon, runnel, malathion, dursban and 2,4-D and found that the higher the molecular weight of the compound the more favourable the effect of adsorption by activated carbon. Similar findings were also reported by other researchers [104,105].

Figure 16. Recirculation through activated carbon [103].

Honeycutt et al. [69] reported that a waste stream containing 100 ppm chlorophenols was reduced to 1 ppm using activated carbon. Giusti et al. [106] reported a carbon activated adsorption of 3.6% and 98.5% for methanol (molecular weight of 32 g/mol) and 2-ethyl hexanol (molecular weight of 130.2 g/mol), respectively. Sarkar et al. [107] reported an adsorbent efficiency of 98% - 99% for the removal of the isoproturon pesticide using powdered activated charcoal. Gupta et al. [108] reported an adsorption efficiency of 70% - 80% using activated charcoal for removing pesticides. Word and Getzen [109] reported that a decrease in pH increased the adsorption of aromatic acid compounds due to enhancement of carbon surface properties.

The activated carbon is very effective in removing pesticides and it does not require extensive monitoring. The disadvantages include: 1) the need for a skilled chemist for field testing, 2) the high cost and 3) this process is only capable of adsorbing solutions with concentrations of less than 1000 ppm [69].

3.10. Composting

This treatment method relies primarily on microbial activity and aeration efficiency. Microorganisms that are naturally occurring in the materials increase significantly in numbers and begin to decompose biodegradable compounds which results in the release of carbon dioxide as well as the production of metabolic heat, causing the temperature of the compost to rise to 60˚C - 70˚C. As the compost temperature increases, three succession of microbes occur: psycrophilis, mesophilis and thermophilis [22].

Racke and Frink [110] reported a complete degradation of carbaryl during the composting of sewage sludge. Petruska et al. [111] achieved a complete degradation of diazinon pesticide using dairy manure compost. Rose and Mercer [112] reported a 100% degradation of parathion insecticide in cannery wastes. Singh [113] reported a degradation efficiency of 96.03% for the endoslufin pesticide after 4 weeks, using composted soil with a moisture level of 38%. Al hattab and Ghaly [97] achieved a captan removal efficiency of 92.4% in the first four days using hay compost.

Several researchers stated that polyhalogenated hydrocarbons, used in pesticides, can be metabolized under anaerobic conditions [114-117]. However, other researchers noted that pesticides may largely persist unchanged during the composting process [110,111,118]. Muller and Korte [118] noted little to no degradation of the aldrin, dieldrin and monolinuron during the composting of sewage waste sludge. Strom [119] noted the presence of chlordanein finished compost from various US municipalities.

3.11. Phytoremediation

In this method plants are used to contain and remove harmfull environmental contaminants as shown in Figure 17 [120]. Kruger et al. [121] reported a degradation efficiency in atrazine of 65% after 9 weeks in soil where Kochi sp. was planted. Coats and Anderson [122] reported that degradation of atrazine, metrolachlor and triflualin was enhanced in soils where the Kochi sp. plant grows. Olette et al. [123] reported that the aquatic plants L. minor, C. aquatic and E. Canadensis were capable of removing 2.5% - 50% of dimethomorph and flazasulfuron present in the water. Buyanovsky et al. [124] noted that the fungi rhizosphere was capable of degrading carbofuran by using it as its carbon source. Gordon et al. [125] noted that 95% of trichloroethylene was removed from wastewater by hybrid polar trees during growing season. Stearman et al. [126] noted that in constructed wetlands, cells with plants were capable of removing 77.1% and 82.4% of simazine and metolachlor, respectively, while cells without plants were only capable of removing 64.3% and 63.2%, respectively. Wang et al. [127] reported that in the first 20 days of plant growth, oilseed rape seedlings were capable of removing 20% of

Figure 17. Phytoremediation to clean up pesticide contaminated grounds [1].

chlorpyrifos pesticide.

3.12. Bioaugmentation

This method uses isolated microbes for the degradation of pesticides. The pesticides are quickly metabolized and converted to products with a lower toxicity under aerobic and anaerobic conditions [22]. Some pesticides are capable of being degraded by certain bacterial strains as their sole nutrient or carbon source. Such microbial reactions are known as mineralizing because of the large amount of carbon dioxide released during metabolism [22].

Dichlorodiphenyltrichloroethane, normally resistant to biodegradation, has been reported to have been metaboilized in an anaerobic microbial culture, followed by an aerobic one [128]. Bhadhade et al. [24] reported that bacteria isolated form soil was capable of degrading 83% - 93% of the organophosphorous pesticide, monocrotophos. Ohshiro et al. [25] reported a 96% reduction in isoxathion from the organophosphourus pestiside by bacteria isolated from turf green soil. Tang and You, [27] reported that the triazophos bacteria is capable of degrading 33.1% to 95.8% of pesticides.

The down side of such a method is the establishment of the microbes in the presence of other microbial populations present in the contaminated soil [22]. Acea et al. [129] noted that the population of the introduced bacteria may be reduced due to susceptibility to predation or starvation.

4. Comparative Analysis

Seven criteria (Table 7) were used for the evaluation of pesticide disposal and treatment methods: 1) containment ability, 2) detoxification ability, 3) time 4) cost, 5) suitable for on farm use, 6) size and 7) water evaporation. Each criterion was then assigned a number from 1 to 20 which was determined by the degree of importance of the criterion. These values were then used to determine the ability of each method to meet a given criterionas shown in Tables 8-25. The sum of the scores obtained from each method were then used to determine its overall performance (Table 26). The results indicated that of the 18 methods of pesticide disposal and treatment evaluated, 9 scored above 80/100 and can be used on farm. These were organic absorbents (97), composting (94), bioaugmentation (92), inorganic absorbents (90), Fenton oxidation (86) O3/UV (83), activated carbon (82), hydrolysis (82) and land cultivation (80). The other methods are not suitable for on farm use as they suffered from containment problems, high cost and variability in detoxifying effectiveness.

5. Conclusion

Pesticides provide the primary means for controlling

Table 7. Criteria used in the comparative analysis.

Table 8. Evaluation criteria for land cultivation.

Table 9. Evaluation criteria for soil pit.

Table 10. Evaluation criteria for plastic pit.

Table 11. Evaluation criteria for concrete pit.

Table 12. Evaluation criteria for evaporative beds.

Table 13. Evaluation criteria for landfilling.

Table 14. Evaluation criteria for incineration.

Table 15. Evaluation criteria for open burning.

Table 16. Evaluation criteria for O3/UV.

Table 17. Evaluation criteria for Fenton oxidation.

Table 18. Evaluation criteria for hydrolysis.

Table 19. Evaluation criteria for KEPG.

Table 20. Evaluation criteria for inorganic absorbents.

Table 21. Evaluation criteria for organic absorbents.

Table 22. Evaluation criteria for activated carbon.

Table 23. Evaluation criteria for composting.

Table 24. Evaluation criteria for bioaugmentation.

Table 25. Evaluation criteria for phytoremediation.

Table 26. Comparative analysis.

organisms that compete with man for food and fibre or cause injury to man, livestock and crops. They played a vital role in the economic production of wide ranges of vegetable, fruit, cereal, forage, fibre and oil crops which now constitute a large part of successful agricultural industry in many countries. After pesticides are applied to the target areas, pesticide residues are removed from applicators by rinsing with water which results in the formation of a toxic wastewater that represents a disposal problem for many farmers. Pesticides can adversely affect people, pets, livestock and wildlife in addition to the pests they are intended to destroy. The phenomenon of biomagnification of some pesticides has resulted in reproductive failure of some fish species and egg shell thinning of birds such as peregrine falcons, sparrow hawk and eagle owls. Pesticide toxicity to humans include skin and eye irritation and skin cancer. Currently, disposal ofpesticidewastewateris carriedoutby: 1) land cultivation, 2) dumpingin soil pits, plastic pits and concrete pits or on land, and in extreme cases in streams near the rinsing operation, 3) use of evaporation beds and 4) land filling. These methods of disposal are totally unsafe as the surface run off will reach streams, rivers and lakes and theinfiltration of the wastewater into the local soil will eventually end up in the ground water. The treatment methods currently used for pesticide containing wastewater include 1) incineration (incinerators and open burning), 2) chemical treatments (O3/UV, hydrolysis, Fenton oxidation and KPEG), 3) physical treatments (inorganic absorbents, organic absorbents and activated carbon) and 4) biological treatments (composting, bio-augmentation and phytoremediation). Some of these methods either require land or are expensive and suffer from variability of effectiveness. Therefore, care must be exercised in the application, disposal and treatment of pesticides. A comparative analysis was performed on 18 methods of pesticide disposal and treatment using six criteria: containment, detoxification ability, cost, time, suitability for on farm use, size and evaporation efficiency. The results indicated that of the 18 methods evaluated, 9 scored above 80/100 and can be used on farm. These were organic absorbents (97), composting (94), bioaugmentation (89), inorganic absorbents (90), Fenton oxidation (86), O3/UV (83), activated carbon (82), hydrolysis (82) and land cultivation (80). The other methods are not suitable for on farm use as they suffered from containment problems, high cost and variability in detoxifying effectiveness.

6. Acknowledgements

This research was funded by the Natural Science and Engineering Research Council (NSERC) of Canada.

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