Abstract
Agricultural waste of bagasse was employed for investigating its lead (Pb2+) removal potential from wastewater of battery manufacturing industry. To optimize maximum removal efficacy of the bagasse, it was thermally modified in the form of biochar. Adsorption kinetics and mechanism including various parameters (contact time, dose and pH) were studied employing biochar prepared from bagasse waste. The optimum adsorption occurred at pH 5 with 140 min. of contact time utilizing 5 g of adsorbent dosage at room temperature (25 ± 3 °C). The maximum removal efficiency was recorded as 12.741 mg g−1 with 75.376% of removal at optimum pH 5 as compared to the initial concentration in the effluent. The result illustrated the most suitable fit was for Langmuir isotherm with monolayer and homogenous adsorption of Pb2+. The kinetics involved in the process was observed to be pseudo-second-order, which indicates chemisorption as a major phenomenon involved in the process. The characterization of the adsorbent biochar was done by SEM, EDX and FTIR analysis that provided details about ultrastructural and functionality of organic moiety present to have porous and rough surface, favoring the adsorption process. The functional groups identified by the FTIR analysis demonstrated involvement of carboxyl groups in Pb2+ binding. Postadsorption elution of metal-loaded bagasse was executed by 0.1 M HNO3 with about 90% of regeneration.
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Introduction
Industrialization and urbanization have all the limits to sustain a healthy and peaceful life on the earth (Li et al. 2017). Among them, aquatic pollution caused by release of various heavy metals (HMs) from different anthropogenic activities is one of the major environmental concerns (Amuda et al. 2007; Ajenifuja et al. 2017). These HMs have the bioaccumulation tendency, non-biodegradable nature and may contaminate the food chain threatening the existence of living beings (Rangabhashiyam and Selvaraju 2015; Poonam and Kumar 2018).
Lead (Pb2+) is one of the most toxic HMs, as lowest concentration in drinking water may cause serious problems to the nervous and reproductive system, kidney, liver, brain and bony tissues (Renner 2010; Andrade et al. 2015). The recommended concentration level of by the Environmental Protection Agency (EPA) is 0.015 and 0.05 mg l−1 in drinking and wastewater, respectively (Salmani et al. 2017; Gil et al. 2018). The main sources of the Pb2+ pollution are battery manufacturing industry, shooting ranges, paint industries, mining processes, chemical manufacturers, surfactants, preservatives, etc. (Xu et al. 2013; Liu et al. 2016; Laidlaw et al. 2017; Mehmood et al. 2017). The removal of Pb2+ from wastewater is accomplished by various conventional techniques like precipitation with hydroxide ion or lime, ion exchange, coagulation, electrochemical process, reverse osmosis and ion flotation (Wang and Chen 2009; Kong et al. 2014; Ehrampoush et al. 2015). But, these methods are expensive as well as produce secondary wastes such as persistent organic pollutants, volatile organic compounds (Salmani et al. 2017; Banerjee et al. 2012). Therefore, one of the most effective and low-cost techniques, adsorption, has attracted researchers for the removal of HMs from water bodies (Trans et al. 2010; Uçar et al. 2015). However, modification of adsorbents for better performance may be a restricting factor in view of consumption of energy and chemicals (Gil et al. 2018). Till now available studies suggest the use of readily available and cheaper materials for example agricultural wastes, industrial wastes and household wastes, algae and fungi for the removal of Pb2+ from water (Saka et al. 2011; Taha et al. 2011; Ibrahim et al. 2012; Reddy et al. 2014; Cheraghi et al. 2015).
Various researchers have used the by-product of sugarcane, i.e., bagasse adsorption of different pollutants including heavy metals, dyes (Joseph et al. 2009; Saad et al. 2010; Said et al. 2013; Gardare et al. 2015; Abdelhafez and Li 2016; Tahir et al. 2016). It is an easily available waste which can be collected from different sugar mills and juice shops. In the present study bagasse was used as adsorbent for the purpose of removal of Pb2+ from battery manufacturing industry effluent. The adsorbent was thermally modified into biochar to enhance the efficiency of adsorbent as thermal treatment increased the surface area and porosity of the adsorbent (Doke and Khan 2017). Adsorption is a surface phenomenon which depends on a number of parameters like pH, contact time, adsorbent dose, initial metal concentration, pore size, temperature, surface area (Buasri et al. 2012; Nguyen et al. 2013; Salmani et al. 2017). The goal of the present study is to assess the effectiveness and performance of bagasse biochar for the removal of Pb2+ from wastewater of battery manufacturing industry effluent. Therefore, the effect of contact time and adsorbent dose on room temperature (25 ± 3 °C) and at pH 5 (optimized) was investigated to optimize the kinetics and isotherms involved in the process. The experiments were performed in batch technique, and adsorption capacity was calculated in the each step for the optimization of the parameters.
Materials and methods
Sample collection
Wastewater was collected from the effluent outlet of battery manufacturing industry situated near Aishbagh Park, Lucknow, UP. The samples were collected in sampling gallons of 10 l during winter season (January 2016) to minimize the influence of microbial activity on physicochemical properties of the wastewater which were examined by following methods of APHA (2005).
Adsorbent preparation
Bagasse was collected from sugar juice shops of Rajnikhand, Lucknow. After collection, it was brought to the laboratory and washed out thoroughly first with tap water after that deionized water for removing dust and unwanted objects. Lastly, bagasse was air-dried for 2 weeks to remove the moisture content. Then, it was subjected to pyrolysis at temperature of about 300 ± 10 °C for 2.5 h. After cooling overnight, the biochar was washed thoroughly with deionized water to remove unwanted ash contents. Thereafter, it was dried in the oven and stored in desiccated condition in airtight containers.
Characterization of the adsorbent
All of the chemical reagents used in the present study were of analytical reagent (AR) grade from E. Merck, Darmstadt, Germany. The adsorbent was characterized by atomic adsorption spectrometer (AAS), Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM) and energy-dispersive X-ray analysis (EDX) studies. The concentration of Pb2+ was determined by AAS (Varian AA240FS). The functional groups present in the biochar before and after treating the wastewater were determined by FTIR (NicoletTM 6700). Surface morphology was observed by SEM (JSM-6490LV, manufactured by JEOL, Japan) micrographs. Further, elemental composition was analyzed by EDX (model no. JSM-6490LV, designed by JEOL, Japan) and elemental composition (C, H, N and S %) was analyzed by CHNS analyzer (model no. Flash EA112 Series, manufactured by Thermo Finnegan). Surface area and pore size of bagasse biochar (before and after treatment) were characterized by Quanta Chrome Nova-1000 surface analyzer instrument under liquid N2 temperature. Further, adsorption–desorption studies were performed in order to determine the evolution of porosity and textural properties and surface are from Brunauer–Emmett–Teller (BET) method. Barrett–Joyner–Halenda (BJH) method was used to evaluate pore diameter and volume and de Boer t-method for the newly generated micropore volume measurement (Venkatesha et al. 2016). The structural integrity of the sample was observed by powder X-ray diffraction (XRD). The data were recorded by step scanning at 2θ = 0.0200/s from 30 to 800 on PANalytical X’ Pert PRO MPD X-ray diffraction with graphite monochromatized Cu K α radiation (λ = 0.15406).
Quantitative evaluation of surface acidic functional groups on the adsorbent
The acidic functional groups present on the surface of biochar were determined by the following Boehm titration method (Boehm et al. 1964; Oickle et al. 2010). 0.05 M NaHCO3, Na2CO3 and NaOH bases were used in this method. 0.5 g of adsorbent was added in 50 ml of three bases. After that, the samples along with blank were shaken for 24 h at 120 rpm and then filtered it to remove extra particles. Thereafter, 20 ml of filtrate from each one was titrated with 0.05 M HCl to neutralize the base completely, and then backtitration was done by the blank solution with 0.05 M NaOH. The phenolphthalein indicator was used to determine the end point of the reaction. All titrations were carried out at room temperature (25 ± 3 °C), and the solutions were made up of Millipore water. The difference between molar NaOH and Na2CO3 was assumed to be the phenolic group content as described by Oickle (2010) and Abdelhafez and Li (2016).
Following steps were used to calculate different surface acidic groups
-
1.
Calculation of surface acidic groups amount (Ax)
$$A_{x} = \frac{{\left( {V_{bx} - V_{x} } \right).M_{\text{HCl}} .2.5}}{{m_{x} }}\,{\text{mol}}\,{\text{g}}\,{\text{m}}^{ - 1}$$where mx = mass of biochar (gm), Vbx = volume (ml) of HCl used for the titration of blank, Vx = volume (ml) used for sample titration of respective bases solution after biochar addition, MHCl = molarity of HCl concentration in moles/lit., 2.5 is a coefficient for decreasing titration sample volume in comparison with reaction sample volume (50 ml/20 ml),
-
2.
Calculation of the amount of different kinds of surface groups
-
a.
Amount of phenolic groups, Aph = A3–A2–A1
-
b.
Amount of carboxylic groups, Aca = A1
-
c.
Amount of carboxylic from lactones hydrolysis groups Ala = A2–A1
where A1, A2 and A3 are amount of surface acidic groups for NaHCO3, Na2CO3 and NaOH, respectively.
-
a.
Moisture and ash content
Moisture content: 1 g of sample was dried for 24 h in an oven at temperature of 100 ± 5 °C until constant weight was gained. Moisture content was calculated using the following formula
where wi = initial weight of the adsorbent (gm), wf = final weight of adsorbent after drying (gm).
Ash content: It was determined with the help of muffle furnace by weighing 1 g of the sample and placing it into a porcelain crucible. The crucible was heated up to 500 ± 5 °C for 5 h. The material was allowed to cool down in a desiccator for 15 min. The ash content was calculated by using the following formula
where W0 = weight of empty crucible (g), W1 = weight of crucible (g) + weight of adsorbent (gm), W2 = weight of crucible (g) + weight of ashed sample (g) (Basu et al. 2017; Poonam and Kumar 2018).
Experimental setup
The adsorption experiment was performed by varying adsorbent dosage from 2.0 to 5.0 g L−1 at an interval of 0.5 g, for 100 ml in 250-ml Erlenmeyer flasks at rotating speed of 120 rpm. The pH was optimized for maximum adsorption by shifting it from 2 to 5 with 0.1 N NaOH and 0.1 N HCl. The contact time was also optimized by varying it from 20 to 140 min at an interval of 20 min, until the maximum adsorption was achieved.
Adsorption rate kinetics
The adsorption kinetics involved is an important parameter to describe the basic traits of a good adsorbent (Wang et al. 2012). It provides the process which controls the sorbate reactions in the solid–solution interface at different time. The present study pseudo-first- and second-order reactions were utilized to describe the adsorption mechanism involved in the Pb2+ removal processes by bagasse biochar (Lagergren 1898; Ho et al. 2000).
The pseudo-first-order kinetic model (Eq. 1) is expressed as
where q1 and qt are the amount of Pb2+ (mg g−1) absorbed at equilibrium and at time t, respectively, and k1 is the first-order rate constant (min−1).
According to Mckay and Ho (1999), pseudo-second-order kinetic model (Eq. 2) is expressed as
Equation (3), modified Ritchie’s second-order kinetic model, is used to calculate the initial sorption rate, h (mg g−1 min−1) (Eq. 4).
where q2 is the maximum adsorption capacity (mg g−1) for the pseudo-second-order adsorption, K2 is the equilibrium rate constant for the pseudo-second-order adsorption (g mg−1 min−1), and h is initial sorption rate (mg g−1 min−1).
Adsorption isotherm studies
The experimental uptake (qe) values obtained from batch assay were analyzed using adsorption isotherm models (Langmuir and Freundlich) and separation factor (RL) at room temperature (25 ± 3 °C) and other optimized conditions, i.e., pH 5, dose 5.0 g and 140 min of contact time.
The linear form of Freundlich adsorption isotherm is given as the following
where Kf and n are Freundlich constants for distribution coefficient and intensity, respectively.
The Langmuir equation is given as
where qe is the equilibrium metal ion concentration, Ce is the equilibrium metal ion concentration in the solution (mg l−1), qmax is the monolayer adsorption capacity of bagasse biochar (mg g−1), and KL is the Langmuir adsorption constant (L mg−1).
Analytical method
The amount of Pb2+ adsorbed was calculated by the following mass balance relationship
and percent removal at the equilibrium (qe) was calculated as the following
where C0 and Ce (mg l−1) are the metal concentrations at initial stage and equilibrium, respectively. v is the volume of the effluent in ml, and w is the weight of the adsorbent in grams(gm).
Desorption study
Desorption experiments were performed with metal-loaded biochar of bagasse to check the reusability of the adsorbent. 0.1 M HCl, HNO3 and H2SO4, and NaOH were used as desorbing eluants. One gram of the Pb2+-loaded adsorbent was added in 100 ml of eluants and incubated for 3 h at 30 °C at 150 rpm.
Results and discussion
Physicochemical properties of battery manufacturing industry effluent
The physicochemical properties of battery manufacturing industry effluent are presented in Table 1. Most of the parameters were found to be beyond the limits prescribed in Bureau of Indian Standards (BIS 10500: 2012) for on land irrigation. pH, temperature and electrical conductivity (EC) affect the ionic concentration of the effluent and influence the chemical reactions in the aquatic environment (Akpomie and Dawodua 2015). Different salts, used in the processes, may be the reason for higher values of pH as well as EC. Chemical oxygen demand (COD), biological oxygen demand (BOD), dissolved oxygen (DO), total dissolved solids (TDS), total suspended solids (TSS) and total solids (TS) define the amount of pollution caused by different organic and inorganic pollutants affecting the water quality. Besides hardness and alkalinity higher concentration of nitrate, phosphate and sulfate may be attributed to the usage of different chemicals and salts during the battery manufacturing processes (Ahmed et al. 2012).
The concentration of Pb2+ in the effluent was found to be 2.393 mg l−1 which exceeded the limit of 0.1 mg l−1 as prescribed by BIS (10500: 2012). Higher concentration of Pb2+ in the water bodies may be harmful for health of flora and fauna (Babel and Kurniawan 2003; Alluri et al. 2007).
Screening of biosorbents
Three thermally modified agrowastes (biochar of bagasse, orange and coir) were observed for their suitability for adsorbing Pb2+ (Fig. 1). Among them, bagasse biochar showed maximum adsorptive removal of 75.38% Pb2+ in comparison with orange (70.36%) and coir (61.98%) for the same adsorbent dosage of 5.0 g l−1. The variation in the adsorption efficiencies may be attributed to variations in the morphology and binding sites of the adsorbents (Petrović et al. 2017).
Characteristics of adsorbent
The proximate and ultimate study of the adsorbents is summarized in Table 2. The ash content was found to be low with average value of 7.337% because of the biochar-producing processes which eliminate the oxygen content. The moisture content was also found to be very low with average value of 1.968% which facilitated the adsorption process. The bagasse biochar was alkaline in nature as pH was found to be 8.967 which could be recognized by the detachment of alkali metal, i.e., Ca2+ as their concentration was found to be moderately high as shown in EDX spectrum of biochar (Fig. 2e). The surface area of the biochar (12.378 m2 g−1) seems to be rough and irregular which was confirmed by SEM image of bagasse biochar (Fig. 2b). Further, the biochar showed comparatively higher C/H and C/N ratio and less C % (Table 1) which suggests that the charring process was not accomplished well with some decomposed matter. This may also be a reason for comparatively lesser specific surface area of the biochar as analyzed by BET. In addition to this, higher values of H and O % indicate availability of binding sites responsible for the successful adsorption of Pb2+ (Table 1). The results were found to be in good agreement with Fernandez et al. (2014); Abdelhafez and Li (2016); and Basu et al. (2017).
SEM and EDX
SEM and EDX images showed the change in the morphology of the adsorbent before and after adsorption process (Fig. 2). The differences in SEM image of (a) bagasse, (b) its biochar and (c) Pb2+-loaded biochar could be clearly visualized. Before charring the surface was uniform and very smooth, and after thermal treatment, it became comparatively rough and irregular increasing the surface area. After adsorption, the space became filled with some irregular, crystalline structures which supported the adsorption of Pb2+ from the effluent. In addition to this, existence of Pb2+ in the EDX spectrum may aslo be considered in the support successful adsorption of the metal (Fig. 2d, e).
FTIR
Adsorption process is affected by the groups and bonds present in the adsorbent. In order to investigate the chemical structure and major functional groups present, which may be responsible for adsorption process, FTIR analysis was carried out (Solum et al. 1995). The spectra of the (a) bagasse, (b) its biochar and (c) Pb2+-loaded biochar are presented in Fig. 3. The broad peaks between 3846 and 3438 cm−1 show the presence of –OH stretching vibrations of cellulose, pectin and lignin in all the three spectra (Guo et al. 2008; Reddy et al. 2014). After thermal treatment, most of the major peaks were disappeared except –CH stretching at 2925.3 cm−1, C=O stretch in ketones represented by broad peak at 1711 cm−1, C=C stretch in alkenes and C=O stretch in secondary amides represented by a sharp peak at 1631 cm−1. The stretching of the chemical bonds is marked by the higher carbon content as well as the organic matter (Abdelhafez and Li 2016). After the adsorption of Pb2+ the peaks were shifted to 1629.7, 1441.67 and 874.9 7 cm−1 representing C=O stretching at C–N stretch in primary amides at C-H and CH2 deformations, respectively. Conversion of secondary amide to primary amide and –CH to C=C is evident of formation and dissociation of bonds and groups through ion exchange or some other mechanisms (Kim et al. 2015). The shift in the functional groups between non-treated and treated adsorbent suggests that the adsorption of Pb2+ might be facilitated by the process of chemisorption resulting in binding of the metal by the nucleophilic functional groups resulting in the formation of metal complex. This process also supported the adsorption of Pb2+ onto the bagasse biochar.
Surface acidic groups
The surface acidic group concentrations of bagasse biochar are represented in Fig. 4. The total concentration of surface acidic groups was 7.033 mol g−1. The carboxylic acidic functional groups occupied maximum concentration of 5.15 mol g−1 in comparison with other phenolic (1.283 mol g−1) and lactonic (0.601 mol g−1) acidic groups. The results of the Boehm titration indicated majority of carboxylic acidic groups occupying 72.963% of total surface acidic groups, followed by lactonic (18.182%) and phenolic (8.855%) groups. These results were in good agreement with those of FTIR analysis, explained earlier.
Effect of pH
The effect of pH on concentration of Pb2+ is presented in Fig. 5. pH is an important controlling parameter in adsorption process as it determines the surface charge of adsorbent, degree of ionization of the adsorbate and extent of dissociation of functional groups present on active sites (Yang and Cui. 2013; Salam et al. 2011). Thus, the effect of H+ ions concentration in the battery manufacturing industry effluent was studied at different pHs at optimized dosage (5.0 g l−1) and contact time (140 min). Above pH 7, precipitation of oxides of Pb2+ was formed; therefore, the study was confined to pH range of 2.0–6.0 (Basu et al. 2017). The optimum pH for the removal of Pb2+ was found to be 5. As the pH of the effluent was increased from 2 to 5, the adsorption capacity of the adsorbent also increased from 3.34 to 3.68 mg g−1. In acidic medium, availability of binding sites increases and removal of H+ ions in the solution facilitates it being replaced by Pb2+ which is termed as chelation. Since Pb has +2 charges, two carbon atoms are involved in chelating/binding of the metal resulting in the formation of metal complex. This may also be the probable reason for the shift in the IR spectra too. At lower pH, there was Coulombic repulsion between positively charged binding sites and cations which suppressed the removal rate, further (Liu and Zhang 2009). The result is in agreement with previous studies for the removal of Pb2+ by bamboo charcoal (Wang et al. 2012), dried water hyacinth (Ibrahim et al. 2012), rapeseed oil cake (Uçar et al. 2015) and strain of Alcaligenes sp. (Jin et al. 2017).
Effect of adsorbent dosage
The effect of adsorbent dosages on the concentration of Pb2+ in battery manufacturing industry effluent is presented in Fig. 5. The experiments were carried out at different dosages ranging from 2.5 to 5 g l−1. For convenience in presenting the data, the initial dose was chosen as 2.5 g l−1 since the removal rate was found to decrease from 66.696 to 64.345% and so on, when the dosage was reduced from 2.5 to lesser. But, when the amount of adsorbent dosage was increased further from 2.5 to 5.0 g l−1, the removal percentage increased from 66.696 to 75.376%. It can be justified by the fact that increasing dose upsurges the number of binding sites for the metal (Gil et al. 2018). The optimum dose for maximum removal of Pb2+ from effluent was recorded 5.0 g l−1. Moreover, when dosage was increased further, removal rate decreased due to overloading and intracellular dissociation phenomenon, which affected the binding capacity of the surface groups (Zhao et al. 2017). These results were in agreement with previous studies performed on many other adsorbents for different metals including Pb2+ (Oluyemi et al. 2012; Kılıç et al. 2013; Reddy et al. 2014).
Effect of contact time
The contact time also plays a major role in the adsorption of metals from effluent. The effect of contact time on the concentration of Pb2+ in the effluent is shown in Fig. 6. The contact time was varied from 20 to 140 min. In initial 20 min about 64.79% of Pb2+ was adsorbed, after which the process slowed down and till 140 min the binding sites of the adsorbents became saturated with 75.376% removal of Pb2+. Thus, the optimum time for the removal of Pb2+ was 140 min. No further change in the concentration of Pb2+ was observed due to exhaustion of the active binding sites. Similar outcomes were also accomplished when adsorbent dosage and pH were optimized. Moreover, the results are in agreement with Uçar et al. (2015).
Adsorption kinetics
The plots of pseudo-first order and pseudo-second order for the adsorption of Pb2+ onto bagasse are presented in Fig. 7. The linear plots of t versus log(qe − qt) and t versus t/qt offer the pseudo-first- and second-order rate constants K1 and K2, respectively, which are calculated by the slope and intercept. The corresponding values of K1, K2, qe and r2 are represented in Table 3.
According to correlation coefficients (r2), the correlation coefficients for pseudo-second-order kinetic model were higher than those of the pseudo-first-order model for Pb2+. This suggests that the adsorption process followed the pseudo-second-order kinetics, indicating adsorption takes place by chemisorptions (Reddy et al. 2014). The results of the present study are in good agreement with previous studies, which also reported that the adsorption process follows the pseudo-second-order kinetics (Uçar et al. 2015; Ibrahim et al. 2012; Wang et al. 2012).
Adsorption isotherm
Adsorption isotherms are used to describe the adsorption equilibrium for wastewater treatments by providing useful information regarding adsorbent surface (Uçar et al. 2015; Naiya et al. 2009). At equilibrium, battery manufacturing industry effluent was allowed to contact with varying dosages of bagasse biochar to examine the maximum loading capacity of the adsorbent used. Adsorption process was justified by applying linear forms of Langmuir and Freundlich isotherms (Langmuir 1918; Freundlich 1906).
The plots of Langmuir isotherm for 1/qe versus 1/Ce and Freundlich isotherm for log qe versus log Ce are presented in Fig. 8. Moreover, values of different parameters for both isotherms and separation factor (RL) are given in Table 4.
Although there is very less difference between both of the isotherms, the results indicated that in comparison with Freundlich (r2 = 0.927), Langmuir isotherm (r2 = 0.9298) better fitted for the adsorption of Pb2+ from battery manufacturing industry effluent. Langmuir model assumes that there were no interactions between solute particles and adsorbent surfaces, and solute particles were distributed in a monolayer carbon surface (Uçar et al. 2015). The monolayer adsorption capacity (qmax) of bagasse biochar for the removal of Pb2+ from battery manufacturing industry effluent was found to be 12.74 mg g−1. The value of qmax was found to be less than previously reported literature; the reason behind this may be the treatment of effluent (with lesser conc. of 2.39 mg l−1 Pb2+) than of known solutions of metals (with higher metal conc.) containing higher concentrations of it (Reddy et al. 2014; Naiya et al. 2009; Wang et al. 2012).
Further, the feasibility of Langmuir isotherm can also be proved by a dimensionless constant, viz. separation factor or equilibrium parameter separation factor (RL) (Hall et al. 1966). It is represented as follows
where C0 is initial metal concentration. If the value of RL is between 0 and 1, then the adsorption is favorable, and if it is higher than 1, then adsorption is unfavorable. If RL = 1, then adsorption is linear, and the RL = 0 indicates irreversible adsorption. In the present study, RL value was less than 0, i.e., 0.603, showing favorable adsorption of Pb2+ onto bagasse biochar.
Desorption and reuse of adsorbent
Desorption process is a reverse process of adsorption and is important to understand its recovering capacity and reusability for commercial application (Zhang et al. 2018). Three acids (HNO3, HCl and H2SO4) and one base (NaOH) of 0.1 M were used as eluants to assess the desorption process. HNO3 was found to be the best eluants to desorb about 90.05% of Pb2+ from the adsorbent (Fig. 9). The result is in agreement with previous studies done by Naiya et al. (2009) and Mondal (2009).
Conclusions
From different agricultural wastes, bagasse was screened as a potential adsorbent for removing from wastewater of battery manufacturing industry effluent. The adsorption process was found to be dependent upon the pH of the medium as well as the contact time and dosage. The maximum adsorption capacity was recorded as 12.741 mg g−1 which is good for removing trace amount of metal from wastewater before disposal to the water bodies. The adsorption capacity of bagasse biochar may be increased by modifying it with various physicochemical methods like charring, addition of chemicals. The results concluded that the bagasse may be used as cost-effective adsorbent for the successful removal of different wastewater generating industries. It may also be utilized in the production of commercial bioadsorbents for removing various heavy metals from industrial effluents.
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Acknowledgements
The authors would like to thank Mr. Shamshad Ahmad, Department of Environmental Science, and Dr. Vertika Shukla, Department of Applied Geology, BBA University, Lucknow, for their help and support.
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Poonam, Bharti, S.K. & Kumar, N. Kinetic study of lead (Pb2+) removal from battery manufacturing wastewater using bagasse biochar as biosorbent. Appl Water Sci 8, 119 (2018). https://doi.org/10.1007/s13201-018-0765-z
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DOI: https://doi.org/10.1007/s13201-018-0765-z