E-ISSN : 2541-5794 P-ISSN : 2503-216X Journal of Geoscience, Engineering, Environment, and Technology Vol 03 No 02 2018 106 Yantrapali, S., Khrisna H and K, Srinivas/ JGEET Vol 03 No 02/2018 A Study on influence of organic ligands on migration of heavy metals through compacted clayey soil Sudheerkumar Yantrapalli 1, *, Hari Krishna P 2 , Srinivas K 3 1 Geotechnical Engineering Division , NIT Warangal, India 2 Department of Civil Engineering, NIT Warangal, India * Corresponding author : sudheerkumar@student.nitw.ac.in Tel.:+91 9866938516 Received: 27 Des, 2017. Revised : 16 Apr, 2018, Accepted: 24 May, 2018, Published: 1 June 2018 DOI: 10.24273/jgeet.2018.3.2.1036 Abstract This paper presents the feasibility study on utilization of locally available clayey soil as Compacted Clay Liner based on its contaminant migration capacity under the presence of organic chemical EDTA (Ethylene Diamine Tetra acetic Acid) which is abundantly released into the environment. Lead, Nickel, cadmium and chromium ions was selected as contaminants and its migration properties are assessed by conducting column studies with a single and multiple heavy metal solution with the EDTA. From the experimental investigations, it is revealed that with the presence of EDTA, the contaminant breakthrough time get reduced due to soluble metal EDTA complex formation. At pH 2, interaction with multi metal, the mobility was increased and the order of mobility was observed as Cr > Cd > Ni > Pb. With the presence of EDTA in multi metal system at pH 2, the order of the mobility was Cr > Ni > Cd > Pb and at pH 7 the mobility of heavy metals were increased the order was Cr > NI > Pb > Cd. This study reveals that locally available clayey soil is capable of retaining heavy metals and it may be used as a compacted clay liner, where organic chemical like (EDTA) ingression is present. Keywords: Clayey soil, Compacted Clay Liner, Lead, Nickel, Cadmium, Chromium, EDTA, Column studies 1. Introduction The rapid growth of industrialization and urbanization, the amount as well as the rate of generation of waste is increasing substantially, thereby insisting us to think about the need of disposal of waste (consisting mainly house hold and industrial rejects) in an effective and scientific way (Rajesh et al., 2014). Basically, the disposed waste comprised of different types of toxic and non-toxic elements i.e. heavy metals, organic and inorganic matter etc. of them, the more emphasis is given to heavy metals which are mainly responsible for contamination of surface and subsurface environment (Marina et al., 2003, Kumar and Singh., 2005; Li et al., 2012). Further, it was observed that, most of the causes of ground water pollution initiated from the landfill area where there was no provision of installing engineered liners and leachate collection system (Goodall and Quigley., 1977). To prevent such surface and subsurface contamination, it is necessary to place a barrier the between waste and surrounding environment (Mulligan et al., 2001). To construct a barrier or liner, with commercially available materials such as bentonite or geo-membranes can be used (Gleason et al 1997). But, using those material landfill lining system may lead to cracking up under elevated temperature and also under aggressive chemicals in landfill. Koerner and Daniel (1993) and Rowe (2005) observed that, using geo-membrane as a bottom liner seems to be ineffective due to the improper handling and placement. High leakage rate has been observed through geo-membrane and geo synthetic clay liner due to tear created in the membrane caused by the improper handling and placing. So, to counter these problems, if locally available clayey soil meeting the basic requirements of landfill liner such as hydraulic conductivity, and good adsorption capacity, it is possible to construct a secure landfill (Mohamedzein et al., 2005). Past findings revealed that the studies on the soil leachate compatibility mainly focused on how heavy metals are being adsorbed by the soil and migrated through. But the adsorption of heavy metals by the soil and migration of heavy metals is unlike under the presence of organic chemicals. The very common organic chemical which is disposed of from household detergents and textile industries is EDTA (Ethaline Diamine tetra Acetic Acid). The volume of EDTA disposed into the environment from these sources is almost 51% (Oviedo and Rodríguez, 2003). The government of Telangana (India) proposed to construct textile industry beside the existing landfill leachate pond. So, disposal of EDTA along with textile industrial waste water on leachate pond causes desorption of metal ions which is retained by the soil then causes the ground water contamination problems in and around landfill areas (Oviedo and Rodríguez, 2003; Chen et mailto:sudheerkumar@student.nitw.ac.in Yantrapali, S., Khrisna H and K, Srinivas/ JGEET Vol 03 No 02/2018 107 al., 2008). Though many researchers have focused on the utilization of EDTA for extraction of heavy metals from the soils and sediments (Reddy et al. 2003; Reddy et al. 2010), but excessive utilization of EDTA may pose severe environmental problems (Peters and Shem, 1992; Peters., 1999). So, utilization of EDTA needs to be scrutinized because this EDTA can influence the mobility of heavy metals through the soil. And the presence of organic and inorganic chemicals in waste water or in landfill leachate may seriously affect the adsorption of various metal ions (Bowers and Huang, 1985). There is a little information available about adsorption behavior of heavy metals with known parameters like type of soil and concentration of organic chemicals present and pH of the leachate. In the present study, efforts were being made to understand the migration of heavy metal ions through the clayey soil with the presence of EDTA. Column studies were performed to calculate the diffusion coefficient from the column data obtained. So, by obtaining these parameters, it may be possible to design safe and secure compacted clay liner systems where the organic chemicals present in the landfill leachate. 2. Transport of chemicals through soil Transport of chemicals through the soil consists of three main process namely, advective transport, diffusive transport and chemical reactions between the chemicals and the soil. The concentration profile of a chemical in the soil medium in 1- D transport equation which can be expressed in equation 1, ∂C ∂t = D R ∂C ∂Z2 − Vs R ∂C ∂Z (1) The solution of the 1-D transport equation was proposed by Ogata and Banks (1961) and rearranged by Shackelford (1994); Mohammad and Anita (1998) for landfill liner application. The solution was expressed in terms of a relative concentration. This is the ratio of concentration as a function of depth and time to the initial concentration of the solution, as expressed in the equation 2. 𝐶 (𝑧,𝑡)) 𝐶0 = 1 2 {𝑒𝑟𝑓𝑐 ( 𝑍−𝑉𝑠 𝑡 2 √𝐷𝑇 ) + exp ( 𝑉𝑠 𝑍 𝐷 ) 𝑒𝑟𝑓𝑐 ( 𝑍+𝑉𝑠 𝑡 2 √𝐷𝑇 )} (2) R: Retardation factor; C: Effluent concentration (mg/L); C0: Influent concentration (mg/L); Z: Thickness of the soil; Vs: Velocity of fluid through soil (m/sec); T: time to achieve breakthrough time (Hr); erfc: complementary error function 3. Materials and methods Locally available Black cotton soil (CH soil) is obtained from Warangal, Telangana, India were used in the study and properties and the chemical composition of the soil is presented in table 1 and 2. Table 1. Properties of the soil Property IS 2720 Clayey Soil Gravel (%) part IV 0 Sand (%) 30 Silt (%) 39 Clay (%) 31 Liquid Limit (%) part V 61 Plastic Limit (%) 21 Plasticity Index 40 Classification (IS) CH MDD (g/cc) part VII 1.7 OMC (%) 19.6 Free Swell Index part XXXX 50 CEC (meq/100g) part XXIV 75 K (10 -10 m/sec) part XVII 0.505 MDD: maximum Dry density; OMC: Optimum Moisture content; CEC: Cation Exchange capacity; K: permeability Table 2. Chemical Composition of the CH soil Soil Composition % Soil Compositio n % SiO2 43.6 K2O 0.63 Al2O3 22.8 MnO 0.47 Fe2O3 14.7 P2O5 0.28 CaO 7.5 Na2O 0.225 MgO 7.3 SO3 0.14 TiO2 1.71 %: Percentage 3.1 Chemicals All the chemicals used in the present study were analytical grade and the stock solution of 1000 mg/l were prepared from the salts. From the 1000 mg/l stock solution, the initial concentration of 30 mg/l of each heavy metal Pb (II), Ni (II), Cd (II) and Cr (VI) prepared. The initial concentration was selected mainly because of the maximum heavy metal concentration present in the leachate. The leachate composition presented in table 3. Table 3. Chemical composition of Leachate Parameter Concentration (mg/l) Nickel (Ni) 37 Chromium (Cr) 22 Cadmium (Cd) 1.1 Lead (Pb) 0.7 The pH of the influent solution was maintained as 2 for Pb, Ni and Cd mainly because, these metals were having less percentage removal at pH 2 (Liu et al, 2010; Soares et al, 2011; Li et al, 2012; Hamadneth et al, 2015). For Cr (VI) the pH was maintained as 7 because of Cr (VI) having less percentage removal at pH 7 (Gosh et al, 2013). When EDTA present along with heavy metals (Pb, Ni, Cd and Cr (VI)), the pH of the solution was maintained as pH 7 because, the EDTA present in 108 Yantrapali, S., Khrisna H and K, Srinivas/ JGEET Vol 03 No 02/2018 the solution have low heavy metal adsorption at pH 7 (Li et al, 2012) and in case of multi heavy metal interaction, the pH was maintained 2 and 7. The pH of the solution was adjusted by using 0.1M HNO3 and 0.1M NaOH solution. 3.2 Experimental procedure Sample preparation and placement in the column Column tests were conducted to determine the transport parameters of the CH soil. The soil samples were prepared by adding deionized water to the air-dried soils to achieve water content 2% wetter than the optimum water content in order to obtain the lowest hydraulic conductivity of soil sample (Daniel, 1994; Benson et al, 1999). Substantially, the samples were compacted in accordance with an adaptation of the standard proctor compaction method using a mould of 6.74 cm diameter and 2 cm height. Fig. 1. Small Scale column setup The sample was permeated initially with DI water in order to achieve the first exposure effect and hence it reduced the hydraulic conductivity of the samples (Shackelford, 1994; Quaranta et al, 1996; Gleason et al, 1997). The flow was induced by maintaining the constant head throughout the experiment. After 24 Hr of Permeation with the DI water, the DI water removed and heavy metal solutions were introduced and then periodically collected the heavy metal effluents and its concentration were analysed by using Agilent made ICP OES. The schematic representation of the column setup used in the investigation is given in Fig. 1. The column was placed on the stand to remain vertically and sufficiently above the floor for outlet. The column tests were observed up to a point when 90% of the breakthrough was achieved. 4. Results and discussion The breakthrough curves are plotted between the relative concentration (C/C0) along ordinate and time along abscissa are shown in figures 2 to 12. The data used for finding breakthrough curves include the results obtained from the column experiments conducted on CH in the presence of single and composite metal solution in the presence of EDTA. The diffusion coefficients for each condition was sown in table 4 and 5.  Single heavy metal interaction Nickel (II) solution Based on the effluent concentration obtained, breakthrough curve is drawn with respect to time calculated from the starting of experiment to the point of collection expressed in hours for CH soil. The breakthrough curves are shown in Fig 2 for CH soil considering only Ni solution as an incoming synthetic pollutant. 0 2000 4000 6000 8000 10000 12000 14000 0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0 1.1 1.2 R e la ti e v e C o n c e n tr a ti o n ( C /C 0 ) Time (Hr) Heavy Metal : Nickel without EDTA pH : 2 C 0 (mg/L) : 30 T 50 (Hr) : 6000 Fig. 2. Breakthrough curve of CH soil for Nickel (Ni) It has been observed from the Fig 2 the breakthrough time required for achieving 50% breakthrough of Ni for CH soil is 1200 hours. This is because of higher cation exchange capacity of CH soil.  Lead (II) solution Based on the effluent concentration obtained, breakthrough curve is plotted with respect to time calculated from the starting of experiment to the point of collection of effluent expressed in hours for CH soil. The breakthrough curve is shown in Fig 3 for CH soil considering only Pb solution as an incoming synthetic pollutant. 0 2000 4000 6000 0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0 1.1 R e la ti e v e C o n c e n tr a ti o n ( C /C 0 ) Time (Hr) Heavy Metal : Lead Without EDTA pH : 2 C 0 (mg/L) : 30 T 50 (Hr) : 3600 Fig. 3. Breakthrough curve for Pb Yantrapali, S., Khrisna H and K, Srinivas/ JGEET Vol 03 No 02/2018 109 Similar trend is observed in case of Pb as in case of Ni i.e., the delayed breakthrough has been found for CH soil. Moreover, from Fig 3, it is also observed that Pb shows more mobility when compared to Ni.  Cadmium (II) solution The breakthrough curve for cadmium is given in Fig 4, in case of CH soil with mentioning of the time required for achieving 50% breakthrough. 0 2000 4000 6000 0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0 1.1 1.2 R e la ti e v e C o n c e n tr a ti o n ( C /C 0 ) Time (Hr) Heavy Metal : Cadmium without EDTA pH :2 C 0 (mg/L) : 30 T 50 (Hr) : 2600 Fig. 4. Breakthrough curve for Cd The Fig 4 shows the time required to get 50% break through is 2600 Hr. finally the order of migration observed for the three heavy metals such as Pb, Ni and Cd has been given based on the breakthrough time. It has been noticed that, compared to Pb and Ni, the Cd is showing more mobility at pH 2 for CH Soil. At pH 2, the order of heavy metal mobility was Ni, Pb and Cd from low mobility to high mobility.  Chromium (VI) solution The column studies were conducted for hexavalent chromium (Cr (VI)) with pH 7. 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0 1.1 1.2 R e la ti e v e C o n c n e tr a ti o n ( C /C 0 ) Time (Hr) Heavy Metal: Chromium pH : 7 C 0 (mg/L) : 30 T 50 (Hr) : 5.5 Fig. 5. Breakthrough curve for Cr (VI) The breakthrough curve obtained from column studies for Cr (VI) were presented in fig 5. The result shows higher mobility of Cr (VI) was observed when compared to mobility of Pb (II), Ni (II) and Cd (II). This is mainly because, as Cr (VI) is present in anionic from, the Cr (VI) will repel with negative charged soil surface as a result it will not adsorbed on the soil surface leads to early migration of the Cr (VI). By considering all the above results, in the term of breakthrough curves in a single metal system, it can be observed that at pH 2, the decreasing order of mobility for heavy metals expressed as Ni < Pb < Cd. This is because, at pH 2, electronegativity of the metal ion plays an important role in getting adsorbed by soil active sites. Higher the electronegativity of metal, the greater chance to get adsorbed by the soil through easier dissociation of H + ion from the functional groups of the soil mineral (Paulo et.al, 2001). The sequence of electronegativity for the three metals are Ni (1.91) > Pb (1.8) > Cd (1.69). The column studies are shows similar behaviour supported by the electronegativity concept. At low pH, the adsorption of Cd is decreased by the protonation of silica and alumina group i.e. Si - O - and Al - O - respectively (Abollino et.al, 2003). On the other hand, the adsorption of Cr (VI) decreases with increase in pH. This is due to increase of negative charge in the soil solid phase (Sherene 2010) with increase in pH which leads to higher mobility of (VI) and also the mobility was expected to be increased by probable decrease in the plastic limit of the soil after interaction of Cr (VI) with the soil. Hence, it increases the hydraulic conductivity of the tested soils due to decrease in the thickness of diffused double layer (Wang P. et al, 2015).  Composite heavy metal system In case of composite metal system, four heavy metals (Pb, Ni, Cd and Cr) have been considered for study. The pH of the final solution was set at 2 by adding 0.1M HNO3. The composite solution was then transferred to soil column for further study. pH 2 has been chosen to eliminate the metal hydroxide compound formation. The breakthrough curves are plotted and shown in Fig 6 based on the results obtained from column tests performed on CH soils. 0 2000 4000 6000 0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0 1.1 R e la ti e v e C o n c n e tr a ti o n ( C /C 0 ) Time (Hr) Lead T 50 : 2000 Hr Nickel T 50 : 600 Hr Cadmium T 50 : 300 Hr Chromium T 50 : 150 Hr CH Soil Multi Metal at pH 2 Fig. 6. Breakthrough curve for Composite heavy metal system 110 Yantrapali, S., Khrisna H and K, Srinivas/ JGEET Vol 03 No 02/2018 From fig 6, it has been observed that the time required to accomplish half breakthrough for multi metal system is less for multi metal system when compared to single heavy metal system for CH soil. The reduction in breakthrough time can be observed for three bivalent metal ions i.e. Ni (II), Cd (II) and Pb (II) and for Cr (VI), the breakthrough time increases when compared to the result obtained in case of single metal system. This is mainly because, the reduction in adsorption for three heavy metals can be stated by considering the competitive effect between the metals with hydrogen ion (H + ). At lower pH, due to the presence of hydrogen ion (H + ) in the soil solution the competition occurs between H + ions and the other three bivalent metals for occupying adsorption sites (Raymond and Yuwaree 1993). As a result, the mobility of three bivalent ions (Pb, Ni and Cd) were increased, which leads to quick breakthrough in case of multi heavy metal system. But in case of Cr (VI) which is present in oxyanionic form, the reverse behaviour can be observed due to the transformation of Cr (VI) ion into Cr (III) ion in presence of H + ion. The equilibrium equation for the yielding of trivalent chromium ion at lower pH is given in equation 3 (Daneshvar et. al, 2002). Cr2O7 2- (aq) + 14H + (aq) + 6e - ----- 2Cr 3+ (aq) + 7H2O (3) The newly formed Cr (III) ion can be retained by the soil through cation exchange process due to its higher positive charge ultimately resulting in greater adsorption of Cr (VI) present in multi metal system at pH 2.  Single heavy metal system with EDTA To find the effect of synthetic organic compound i.e. EDTA on the mobility of heavy metals passing through the CH soil. The same procedure was then followed as in case of single metal system without the presence of EDTA. The breakthrough curve obtained based on the available data for each heavy metal separately in the presence of EDTA are presented in figures 7 to 12.  Nickel (II) solution with EDTA Based on the effluent concentration of Ni (II) obtained, the breakthrough curve was plotted and presented in Fig 7 for CH soil. 0 150 300 450 600 750 900 1050 1200 0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0 1.1 1.2 R e la ti e v e C o n c e n tr a ti o n ( C /C 0 ) Time (Hr) Heavy Metal : Nickel pH :2 C 0 (mg/L) : 30 EDTA : 1.0 mM T 50 (Hr) : 3750 Fig. 7. Breakthrough curve for Ni (II) in presence of EDTA From Fig 7 it is observed that, in the presence of EDTA, the time for achieving 50% breakthrough is reduced compared to the absence of EDTA in single metal system. It can be concluded that the chelating ability of EDTA increase the solubility of Ni by forming complex product (Kim et.al. 2003).  Lead (II) solution with EDTA The breakthrough curve for Lead (II) in the presence of EDTA is represented in this context. The time required for attaining half breakthrough is also approximately mentioned by sorting it out from the breakthrough curve. The breakthrough curve for CH soil are shown in Fig 8. 0 2000 4000 0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0 1.1 1.2 R e la ti e v e C o n c n e tr a ti o n ( C /C 0 ) Time (Hr) Heavy Metal : Lead with EDTA pH : 2 C 0 (mg/L) : 30 mg/L EDTA : 1 mM T 50 (Hr) : 2230 Fig. 8. Breakthrough curve for Pb (II) in presence of EDTA From fig 8, it is observed that, the mobility of Pb (II) increased in the presence of EDTA due to the Pb EDTA complex formation. The effect of EDTA complexation with metal ion can be quite presumed based on the obtained breakthrough data.  Cadmium (II) solution with EDTA In presence of EDTA, the mobility of Cd (II) can be shown through the breakthrough curve plotted on the basis of the results obtained from column test. The time required for achieving 50 % breakthrough shown in Fig. 9. The breakthrough curve was presented with respect to time expressed in hours. Cd (II) was also not an exception case from the other two bivalent metal ions (Pb and Ni). But the reduction in time for achieving half breakthrough due to increase in mobility of metal ions through the formation of stable metal- EDTA complex product was more in case of Cd (II) compared to Ni (II) and Pb (II) . In the presence of EDTA, the increasing order of mobility was observed as: Cd (II) > Pb (II) > Ni (II). The observed behaviour of the three bivalent metals (Pb, Ni and Cd) can be explained by employing of complexation constant which determines the stability of metal- EDTA complex. The stability constants of Cd, Pb and Ni are 16.5, 18 and 18.6 respectively. The higher the value of complexation constant, the greater will be the chance of forming more stable metal- EDTA complex. The increasing order of the stability constant in case of heavy metal ions is as follow: Cd (II) < Pb (II) < Ni (II) and Yantrapali, S., Khrisna H and K, Srinivas/ JGEET Vol 03 No 02/2018 111 from this as stability constant of metal EDTA complex increased, the mobility of heavy metal is reduced (Nastaran and Alain, 2009). 0 50 100 150 200 250 0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0 1.1 1.2 R e la ti e v e C o n c e n tr a ti o n ( C /C 0 ) Time (Hr) Heavy Metal : Cadmium pH : 2 C 0 (mg/L) : 30 EDTA : 1.0 mM T 50 (Hr) : 440 Fig. 9. Breakthrough curve for Cd (II) in presence of EDTA  Chromium (VI) solution with EDTA The breakthrough curve for hexavalent chromium solution in the presence of EDTA have been shown in Fig. 10. Which shows the time required for 50 % breakthrough for CH soil at pH 7. 0 50 100 150 200 250 0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0 1.1 1.2 R e la ti e v e C o n c e n tr a ti o n ( C /C 0 ) Time (Hr) Heavy Metal : Chromium pH : 7 C 0 (mg/L) : 30 EDTA : 1.0 mM T 50 (Hr) : 105 Fig. 10. Breakthrough curve for Cr (VI) in presence of EDTA From fig 10, it was observed that, the mobility of Cr (VI) is reduced in the presence of EDTA in case of CH soil when compared with without EDTA condition. This is mainly because, at greater pH the presence of hydroxyl ion (OH - ) may compete with EDTA for complexation with the metal ions which tends to hydrolyse and precipitate as hydroxides (Jose et.al. 2014).  Composite heavy metal system with EDTA The column tests were performed on composite heavy metal system (i.e. Pb (II), Ni (II), Cd (II) and Cr (VI)) in the presence of EDTA at two different pH (2 and 7) to know the breakthrough behaviour of heavy metals. All the results obtained from each test are represented in the form of breakthrough curves which are plotted and presented in Fig 11 and 12.  Composite heavy metal with EDTA at pH 2 Based on the concentration of effluents and the time of collection of effluents emitting from the soil columns, the breakthrough curves were plotted and further represented in the context. 0 2000 4000 0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0 1.1 R e la ti e v e C o n c n e tr a ti o n ( C /C 0 ) Time (Hr) Lead, T 50 :1300 Hr Nickel, T 50 :900 Hr Cadmium, T 50 :2010 Hr Chrmoium, T 50 :400 Hr CH soil Multimetal EDTA pH 2 Fig. 11. Breakthrough curve for Composite heavy metal in the presence of EDTA Form the Fig. 11, it is observed that, there are many variations in the results that can be observed in multi metal system under the influence of EDTA when compared to single metal system in the presence of EDTA. This is mainly due to the competitive effect existing between Ni (II) and Pb (II) with other metals and H + ion present in multi metal system and higher complexation constants prevailing in the metal- EDTA complexation reactions for both bivalent metals, the mobility is enhanced in case of Ni (II) and Pb (II) for CH Soil. In case of Cd (II), this is mainly due to the low stability constant of Cd (II) - EDTA complex product and shortage of free EDTA ions available for complexation while having higher affinity of EDTA towards other bivalent ions. For Cr (VI), after transforming into trivalent ion i.e. Cr (III) the chance for forming complex with EDTA is reduced due to increase in its ionic radius compared to Cr (VI) (Jose et. al 2014).  Composite heavy metal with EDTA at pH 7 Comparative analyses have been done based on the results obtained at two different pH (2 and 7) with supporting expectable reasons which more or less confirm to the explanations provided by the researchers. The break through characteristics of composite heavy metals in the presence of EDTA at pH 7 was presented in Fig. 12, from Fig 12, it is observed that, the break through time is reduced significantly in the presence of EDTA at pH 7 condition when compared with composite heavy metals at pH 2 condition in the presence of EDTA. This is due to the formation of metal EDTA complexes that exist in the solution in the form of negative charged molecule (Bradl 2004), as a result of the negative charged soil surface is competing with the metal EDTA complex leads to the early migration of heavy metals through the soil. 112 Yantrapali, S., Khrisna H and K, Srinivas/ JGEET Vol 03 No 02/2018 0 500 1000 1500 2000 2500 0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0 1.1 1.2 R e la ti e v e C o n c e n tr a ti o n ( C /C 0 ) Time (Hr) Lead T 50 :850 Hr Nickel T 50 :450 Hr Cadmium T 50 :1020 Hr Chromium T 50 :150 Hr BC Soil Multi Metal EDTA pH 7 Fig. 12. Breakthrough curve for Composite heavy metal in the presence of EDTA  Diffusion Coefficient (D*) The diffusion co-efficient (D*) are calculated by using equation 2 on the basis of T50 (time required to achieve 50 % breakthrough) obtained from each breakthrough curve for the corresponding case (Ramakrishna et.al. 2011). The parameter D* is having greater significance in designing and checking the effectiveness of the landfill liner.  Diffusion coefficient (D*) for Black cotton soil (CH) The effective diffusion coefficient (D) calculated for single heavy metal solution interaction is presented in the table 4. Table 4. Diffusion coefficient for Single metal solution Single Heavy metal without EDTA pH Heavy metal D* (m 2 /sec) 7 Cr 2.45x10 -08 2 Cd 4.16x10 -11 2 Pb 3.50x10 -11 2 Ni 2.10x10 -11 Single Heavy metal with EDTA 7 Cr 1.15x10 -09 2 Cd 2.74x10 -10 2 Pb 5.39x10 -11 2 Ni 3.18x10 -11 From this table it is observed that the diffusion coefficient is reduced about 1.54, 1.51 and 6.58 times for Pb (II), Ni (II) and Cd (II) respectively after EDTA present in the influent solution. This is mainly because, when the influent solution passes through the soil column, because of the alkali nature of the soil, the solubility of the metal EDTA complex is increasing as a result, the mobility of the heavy metal increasing. In case of the Cr (IV), after interacted with EDTA the diffusion coefficient is reduced by 21 times, this is due to the this Cr (IV) reduces to Cr (III) after interacting with EDTA and this Cr (III) forms the precipitated wit in the soil due to the alkali nature of the soil and these precipitates are blocking the flow paths in the soil that leads the decrease in the mobility of Cr (VI) through the soil column. The table 5 shows the diffusion coefficients of CH soil interacted with multi metal solution with and without EDTA at two different pH conditions (2 and 7). Table 5. Diffusion coefficient for Multi-metal solution Multi Heavy Metal at pH 2 Heavy metal D* (m 2 /sec) Cr 6.0x 10 -10 Ni 2.01x 10 -10 Pb 6.10x10 -11 Cd 4.02x10 -10 Multi Heavy Metal EDTA at pH 2 Cr 3.02x10 -10 Ni 1.34x10 -10 Pb 9.25x10 -11 Cd 5.98x10 -11 Multi Heavy Metal EDTA at pH 7 Cr 8.6x10 -10 Ni 2.68x10 -10 Pb 1.42x10 -10 Cd 1.180x10 -10 From this table it is observed that, the mobility of Pb (II), Ni (II) and Cd (II) increased about 1.74, 9 and 9.5 time when compared to single metal solution. The mobility of Cr (VI) decreased when compared with the single heavy metal solution. This is mainly due to the complex formation with the other heavy metals. From the table 5 it can also observed that, the mobility is decreased when the CH soil interacted with the multi metal solution with EDTA at pH 2 this is mainly because, at pH 2 most of the metal EDTA complexes are not that much strong and these metal EDTA complex will get precipitated at pH 2 that leads to decrease in the mobility of metal trough the soil column. The multi metal solution with EDTA at pH 7, the mobility got increased about 2.3, 1.3 and 1.43 times respectively for Pb (II), Ni (II) and Cd (II) the mobility got decreased about 3 times because of the competition between metal EDTA complexes. Table 5 also shows the mobilization of heavy metals through the soil column under the influence of EDTA at pH 2 and 7. The mobility of heavy metals are increased about 1.53, 2, 1.97 and 2.84 times respectively for Pb (II), Ni (II) and Cd (II) compared with pH 2 condition. This is mainly because, the stable metal complex formation lead to early migration of the heavy metal migration through the soil column. These diffusion coefficients can be effectively used to predict the migration of heavy metals along the thickness of the liner (1-D case). Hence, it also provides a quite Yantrapali, S., Khrisna H and K, Srinivas/ JGEET Vol 03 No 02/2018 113 precise idea about choosing the appropriate design specifications of the liner that can be installed in the landfill area under the prevailing environmental conditions. Although the values determined by using the advective- diffusion equations can reliably be used, somehow it over predicts the value of diffusion coefficient as the seepage velocity term included in the equation was calculated by considering initial hydraulic conductivity. 5. Conclusions 1. Breakthrough behaviour of heavy metal depends upon several factors such as pH of the soil and heavy metal solution, initial concentration of the metal solution, bed depth of the liner provided in the landfill, presence of organic ligand in the landfill waste, existence of other heavy metals and physical and mineralogical properties of the soil. 2. At lower pH, the adsorption of metal ions mainly takes place through cation exchange process which in-turn depends upon the electronegativity of the metal. While at higher pH, immobilization of heavy metals occurs through hydroxide precipitate formation which also indirectly depends upon the radius of first hydrolyzed product of metal. 3. In multi-metal system, the cause for attaining quick breakthrough can be explained by the competitive effect between the other heavy metal ions and hydrogen ion (H + ) for occupying the adsorption sites of the soil. 4. The chelation effect of EDTA to form metal- EDTA complex product depends upon various factors such as the type of metal, the size of metal ion, pH of the solution and magnitude of complexation constant which determines the rate of complexation reaction. 5. Soil having higher cation exchange capacity (CEC) generally increases the breakthrough time by providing more adsorption sites for metal ions. CH soil is having higher cation exchange capacity that makes it capable of retaining more bivalent metal ions (Pb, Ni and Cd) considered for study. But for hexavalent chromium ion, mobility is increasing in case of CH soil due to repulsion between its oxyanionic form and negative charges on the soil surface. Single Heavy metal solution: 1. For CH soil, the order of selectivity for three heavy metals (Pb, Ni and Cd) is observed as Pb > Ni > Cd at pH 2. For Cr (VI), it shows more mobility at pH 7. For bivalent metal ions pH 2 was considered as that pH at which immobilization of metals can possibly occur through cation exchange process rather than hydroxide formation and same case happens for hexavalent chromium (VI) at pH 7. Although the effective diffusion coefficients (D*) itself show the greater mobility in case of Cr (VI) at pH 7 compared to other three heavy metals. 2. In presence of EDTA, the breakthrough time get reduced due to soluble metal-EDTA complex formation. The order of mobility for bivalent ions in this case is observed as Ni Pb > Cd at pH 2. The effect of EDTA on mobilizing Cr (VI) at pH 7 was comparatively more pronounced from the aspect of effective diffusion coefficient (D*) than other heavy metals at pH 2 condition. 3. CH soils show almost same breakthrough behaviour for four heavy metals in presence of EDTA. Multi-Heavy metal solution: 1. 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Effect of pH on leaching behaviour of compacted cement solidification/ stabilization lead contaminated soil. Environmental Progress and Sustainable Energy, 35(1), pp. 149 155. 1. Introduction 2. Transport of chemicals through soil 3. Materials and methods 3.1 Chemicals 3.2 Experimental procedure 4. Results and discussion  Single heavy metal interaction  Lead (II) solution  Cadmium (II) solution  Chromium (VI) solution  Composite heavy metal system  Single heavy metal system with EDTA  Nickel (II) solution with EDTA  Lead (II) solution with EDTA  Cadmium (II) solution with EDTA  Chromium (VI) solution with EDTA  Composite heavy metal system with EDTA  Composite heavy metal with EDTA at pH 2  Composite heavy metal with EDTA at pH 7  Diffusion Coefficient (D*)  Diffusion coefficient (D*) for Black cotton soil (CH) 5. Conclusions REFERENCES