Journal Information
Vol. 8. Issue 1.
Pages 75-86 (January - March 2019)
Download PDF
More article options
Vol. 8. Issue 1.
Pages 75-86 (January - March 2019)
Original Article
DOI: 10.1016/j.jmrt.2017.05.016
Open Access
Efficiency of immobilized Zea mays biomass for the adsorption of chromium from simulated media and tannery wastewater
Qaisar Manzoora, Arfaa Sajida, Tariq Hussainb, Munawar Iqbala,
Corresponding author
, Mazhar Abbasb, Jan Nisarc
a Department of Chemistry, University of Lahore, Lahore, Pakistan
b Jhang-Campus, University of Veterinary & Animal Sciences Lahore, Pakistan
c National Center of Excellence in Physical Chemistry, University of Peshawar, Peshawar 25120, Pakistan
This item has received

Under a Creative Commons license
Article information
Full Text
Download PDF
Figures (8)
Show moreShow less
Tables (2)
Table 1. Pseudo-first-order and pseudo-second-order kinetic models for Cr(III) and Cr(VI) adsorption onto corn cob (native and immobilized) biomasses.
Table 2. Langmuir and Freundlich isotherms for Cr(III) and Cr(VI) adsorption onto corn cob (native and immobilized) biomasses.
Show moreShow less

In view of adsorption efficiency of modified agricultural biomasses, present study was conducted to appraise the chromium [Cr(III) and Cr(VI)] adsorption capacities of corn cob immobilized biomass. Corn cob biomass was immobilized in calcium alginate bead and process variables such as Cr ions initial concentrations, pH, dosage and contact time were optimized. The Cr(III) and Cr(VI) were adsorbed up to 277.57mg/g and 208.6mg/L onto corn cob immobilized biomass under optimized conditions of process variables. Both Cr ions followed Langmuir isotherm and the pseudo-second order kinetic model. Optimized conditions were employed for Cr adsorption from tannery effluents and up to 64.52% and 55.98% Cr(III) and Cr(VI) were removed, respectively. The immobilized corn cob biomass was run up to 5 repeated adsorption–desorption cycles and 0.98% and 1.51% adsorption efficiencies were reduced at the end of 5 adsorption–desorption cycles of Cr(III) and Cr(VI), respectively. NaOH (0.1M) efficiently desorbed the Cr ions from corn cob immobilized adsorbent and up to 79.8% and 86.0% Cr(III) and Cr(VI) ions were recovered respectively. Results revealed that the immobilization is a viable technique for the modification of native agricultural biomass for efficient remediation/sequestration of metal ions from industrial effluents.

Corn cob
Chromium ions
Full Text

The waste agriculture biomasses have been extensively studied for adsorption and commercial adsorbents have been developed based on agricultural waste biomasses. More recently, the modification (immobilization/bio-composites preparation) attracted the attention of environmentalists in view of their excellent physico-chemical properties and adsorption efficiencies [1–14]. Native biomass have disadvantages such as un-even particle size, low density, poor mechanical strength, rigidity and instability under variable conditions [6,15]. So far, the deficiencies of native biomass can be minimized by immobilizing the biomass with suitable matrix, which offer various advantages, i.e., occupy less volume, easier to handle during processing, stabile for multiple cycles and stable under different conditions, i.e., salinity, metal toxicity, pH and temperature. In view of advantages of immobilization, the modification/immobilization has emerged an attractive alternative to produce efficient adsorbents [6,16]. Number of studies have been performed to study immobilized biomass performance and based on adsorption capacity, stability and recycling, the immobilized/modified materials found to be excellent versus native biomasses [17–25]. To date, alginate beads, carrageenan beads, polyurethane foam, agarose beads, agar beads, polyacrylamide gels, silica gel, capron fibers, ceramics material, cellex-T, anionexchange resin, amberlite, ionexchange resin, controlled-pore glass, Luffa cylindrical sponge, graphene nanosheets, chitosan nanofibers, polyvinyl foams, and filter paper have been used as a matrix and employed for the removal of metal ions (Ni, Cu, Cd, Zn, Au, Cr, Hg, U, Pb, Al, Co, Fe, Mn, Pd, Pt, Ag), inorganic ions (ammonium, phosphate, nitrate, nitrite, phosphorus, etc.) and other organic compound including dyes [6,13,14,16,26–32].

Maize (Zea mays L) is a Pakistan's third most important cereal crops after wheat and rice. It is used as food, feed as well as wet milling industrial agent. Pakistan environmental conditions are very favorable and for domestic need, surplus amount of maize is produced [33]. Corn cob is produced as a waste material from maize during processing. Small amount of corn cob waste is used as a fuel (in kitchen for cooking purpose) and other is wasted in huge quantity [34]. In view of current scenario of heavy metals contamination of water bodies, there is need to explore alternate adsorbents for the remediation purposes. So far, the possibility to use modified corn cob waste biomass as adsorbent is of great interest, which has not been studied previously for Cr ions adsorption.

In the present investigation, corn cob powder was immobilized in Ca–alginate beads and adsorption efficiency of prepared adsorbent was evaluated for Cr ions. Various process variables such as Cr ions initial concentrations, contact time, pH and adsorbent dosage. Equilibrium and kinetic models were employed to evaluate the adsorption behavior of Cr(III) and Cr(VI) on to modified corn cob adsorbent. SEM and EDX techniques were employed as cauterization techniques. The recycling ability of prepared adsorbent was also checked using NaOH as desorbing agent.

2Material and methods2.1Chemical and reagents

The chemical used like K2Cr2O7 (99%), Cr(NO3)3 (99%), NaOH (97%), HCl (37%), acetone (99%), CaCl2 (97%), Na-alginate and Cr(III) and Cr(VI) standards were purchased from Sigma–Aldrich (Germany). Stock solutions of Cr(III) and Cr(VI) were prepared by dissolving salts of Cr(NO3)3 and K2Cr2O7 in ultra-pure water and used to prepare working concentrations. Ultra pure water with a resistivity of 18.2MΩ cm (Milli-Q system, Millipore) was used for the preparation of solution. The siever (OCT-DIGITAL 4527-OI), orbital shaker incubator (PA 250/25.H), analytical balance (Shimadzu, AW 220), pH meter (HI-8014 Hanna), grinder (Moulinex, France) and spectrophotometer (CE Cecil 7200, UK) were used throughout the study (otherwise stated).

2.2Biomass preparation

Waste maize corn cob was collected from Rafhan Private limited, Faisalabad Pakistan. Corn cobs were washed extensively with water, dried in sunlight followed by oven dried at 60°C for 72h. The dried biomass was chopped, grinded and sieved through Octagon siever (OCT-DIGITAL 4527-01) to get even particles. The particle fraction of 0.25mm was collected and used for adsorption and immobilization purpose.

2.3Immobilization procedure

Na-alginate (2%, w/v) was dissolved in hot water (60°C) with continuous stirring and slurry, thus produced was cooled down to room temperature and 1g of corn cob powder was added and homogenized by agitation and extruded into 0.1M CaCl2 solution with the help of a syringe. The beads thus formed (3mm) were kept at 4°C for 2h, washed thoroughly with ultra-pure water and subjected to Cr(III) and Cr(VI) adsorption from aqueous solution as well as tannery effluents.

2.4Adsorption procedure

Various process variables were optimized for maximum Cr ions adsorption. pH effect was studied in the range of 1–6 pH and other conditions of adsorbent dosage (0.1g), contact time (24h) and metal ions concentration (100mg/L) were constant. The concentration of Cr ions 25–1000mg/L was studied, whereas 0.1g adsorbent dose, 24h contact time and pH 5 (Cr(III)) and 2 (Cr(VI)) were constant. The contact time was studied in the range of 10–1440 using adsorbent dose 0.1g, Cr ions initial concentration of 100mg/L and pH (5 and 2 for Cr(III) and Cr(VI), respectively). For batch experiments, 100mL solution, shaking speed 100rpm and room temperature (25°C±2) were constant. For adsorption experiments, respective amount of adsorbent was mixed with Cr solution and pH was adjusted using 0.1M NaOH/HCl, then the flasks were placed in orbital shaker for stipulated time periods. The Cr(III) and Cr(VI) residual concentrations were determined by using Atomic absorption spectrophotometer (A Analyst 300, PerkinElmer). The adsorbent was separated by centrifugation and the Cr adsorbed/unit mass was calculated. The qe values both for native and immobilized adsorbents were estimated using relation shown in Eq. (1)[35].

where, C0 is the initial concentration of chromium (mg/L), C is the equilibrium concentration (mg/L), V is the volume of solution (mL) and m is the adsorbent dose (g).

All adsorption experiments were run in triplicate and data thus, obtained was reported as mean ± SD.

2.5SEM and EDX analysis

The loaded and un-loaded corn cob adsorbents (native and immobilized) were characterized by SEM and EDX techniques as precisely reported elsewhere [36].

2.6Desorption study

The corn cob immobilized adsorbent, desorption ability was checked in 0.1M NaOH solution. The loaded biomass was dried and placed in contact with 0.1M NaOH solution and stirred for 24h at 100rpm and dye desorbed was estimated (Eq. (2)). The adsorption–desorption was performed up to 5 cycles.

where qd (%), D and R are representing desorption capacity, dye adsorbed and dye recovered (desorbed), respectively.

3Results and discussion3.1Effect of pH

Effect of pH on Cr adsorption is depicted in Fig. 1(A and B), which was studied in the range of pH 1–6 for Cr ions initial concentration of 100mg/L, contact time 120min and adsorbent dosage 0.1g. Cr ions removal efficiency was found to be pH dependent. The Cr(VI) adsorption was higher at pH 2 (40.7mg/g) and by increasing pH, the adsorption capacity decreased linearly until pH 6. Cr(III) adsorption increased constantly up to pH 5, which was maximum at pH 5 (45.97mg/g). The behavior of corn cob native and immobilized adsorbent was similar, however, immobilized biomass showed higher adsorption capacity at all pH values versus native corn cob biomass. The variable behavior of Cr adsorption at different pH values was due to different surface chargers at different pH values. It is well known that the HCrO4 ion is the dominant specie of Cr(VI) in the pH range of 2–3 and by increasing the pH, this dominant specie is converted in to CrO42− ions. Secondly, the surface bears positive charges at lower pH [37] and resultantly, the Cr(VI) adsorption was higher at pH 2, which decreased by increasing the pH, so far, the electrostatic interactions were higher at pH 2 for Cr(VI) and vice versa. These findings are in line with previous studies that Cr(VI) adsorption was higher under acidic conditions and deceased as the pH moved toward neutral value [6,38]. Different adsorbents also showed similar behavior for Cr adsorption, i.e., Rosa damascena. This can be correlated this behavior of Cr(VI) adsorption with HCrO4 ions at lower pH and decreasing adsorption of Cr(VI) was correlated with change in surface charges, which led to repulsive forces between Cr(VI) ions and adsorbent surface and the Cr(VI) adsorption decreased. For Cr(III), maximum adsorption was observed at pH 5, which was due to the formation of Cr(OH)2+, Cr(OH)2+, Cr2(OH)24+ and Cr3(OH)45+ species [39]. At higher pH, these species are adsorbed favorably. The Cr(III) less adsorption at lower pH values was due to the competition of Cr ions with protons, repulsion between protonated adsorbent surface and ions [40,41]. At higher pH, the protonation decreased and resultantly, the Cr(III) adsorption enhanced, which was highly significant at higher pH [39]. Deprotonation at higher pH values may also affect the Cr(III) adsorption. The adsorption capacities of native corn cob biomass and immobilized corn cob showed a significant difference for the adsorption of both Cr(III) and Cr(VI) ions. Corn cob native and immobilized adsorbents furnished maximum sorption capacities of 34.68mg/g and 45.97mg/g at pH 5 and 40.7 and 27.18mg/g was at pH 2 of Cr(III) and Cr(VI), respectively. This behavior of native and immobilized biomass can be attributed with different nature of adsorbents because immobilization offers new sites for the binding of ions by inducing cross linking between polymeric matrix and biomass. These findings are in line with already documented studies for native versus immobilized adsorbents i.e., R. damascena phytomass waste biomass [42], cyanobacterial mats [43], termitomycesclypeatus[44], Sphaerotilus natans[45] and immobilized Cunninghamella elegans[46].

Fig. 1.

Effect of pH on chromium adsorption onto native and immobilized corn cob adsorbents (pH 1–6, Cr ions initial concentration 100mg/L, contact time 120min and adsorbent dosage 0.1g).

3.2Effect of metal ions initial concentration

The effect of Cr ions initial concentration was studied in the range of 25–1000mg/L both for Cr(VI) and Cr(III) using adsorbent dose (0.1g) and pH (5 and 2 for Cr(III) and Cr(VI), respectively) and 24h contact time. The adsorption responses of both native and immobilized corn cob adsorbents are shown in Fig. 2(A and B). As it can be seen from results, by increasing the Cr ions initial concentration, the adsorption capacities increased, whereas percentage removal decreased as the initial concentration increased (Fig. 3(A and B)). In case of Cr(III), the adsorption capacities were recorded to be 13.77 and 277.57 (mg/g) for initial concentrations of 25 and 1000 (mg/L), respectively, and percentage removal of 55.08 and 27.76 (%) was recorded, which indicates that by increasing the Cr ions initial concentration, the adsorption capacity increased and percentage adsorption was decreased. For Cr(VI), similar trend was observed, however, the adsorption capacities and percentage removal was low versus Cr(III). The removal efficiency of 208.6mg/L for Cr(VI) ions initial concentration of 1000mg/L was recorded, which reduced to 12.61mg/L for initial concentration of 25mg/L in case of corn cob immobilized adsorbent. The enhanced adsorption at higher concentration was due to the driving forces to overcome mass transfer resistance between the liquid and solid phases [4,5,2]. At extremely higher initial concentration, the available binding sites were saturated and the adsorption depends on the initial concentration [35]. The probability of interaction of ions with binding sites was reduced, which restricted the adsorption process. Therefore, for effective adsorption, the ions in solution that interact with the binding sites are important. The possible reason for this behavior can be explained on the basis of unsaturation of bindings sites and at higher concentration the competition between ions and available binding sites was increased and hence, the complexation of ions was difficult, which slowed down the adsorption process [4,5,2]. Similar trend of Cr adsorption have also been reported previously as a function of Cr ions initial concentration for dead fungal biomass of Phane-rochaete crysosporium[47], immobilized C. elegans[46] and Cyanobacterium Oscil[48].

Fig. 2.

Effect of chromium ions initial concentration on chromium adsorption onto native and immobilized corn cob adsorbents (Cr ions initial concentration 25–1000mg/L, adsorbent dose 0.1g and pH (5 and 2 for Cr(III) and Cr(VI), respectively) and 24h contact time).

Fig. 3.

Percentage recovery of chromium ions at different chromium ions initial concentrations using native and immobilized corn cob adsorbents (explanations as given in Fig. 2).

3.3Effect of contact time

Effect of contact time on Cr(III) and Cr(VI) was studied in the range of 10–1440min and adsorption responses are shown in Fig. 4(A and B) for corn cob native and immobilized biomass, respectively. The Cr ions adsorption was rapid up to 240min followed by slow adsorption up to 400min and beyond this, the Cr ions adsorption stopped. The adsorption of Cr ions took place in two distinct steps, i.e., an initial fast step (shorter duration) followed by slower adsorption (longer duration). Lower adsorption at latter stage may be due to the difficulty faced by metal ions to occupy the remaining vacant binding sites. Secondly, slow adsorption in second phase might be due to intraparticle diffusion process [49]. The fast adsorption of Cr ions was due to availability of binding sites, which exhausted as the adsorption process proceeded with time and resultantly, adsorption slowed down. Therefore, the concentration gradient between ions and adsorbent was changed with time [50,51]. The corn cob native and immobilized biomasses also showed variable behavior or Cr(III) and Cr(VI) ions, However, immobilized corn cob response was promising versus native corn cob biomass. The sorption capacity for Cr(III) was 46.99mg/g (immobilized) >34.61mg/g (native). The Cr(VI) adsorption was 42.93mg/g (immobilized) >28.26mg/g (native). Similar trend of chromium adsorption using different biomasses have been reported previously for different biomasses, i.e., sugarcane bagasse [6], R. damascena phytomass [42], Chlorella biomass [52], dead fungal biomass of P. crysosporium[47], pistachio hull [37], O. americanum seeds biomass [53], banana peel [54], orange (Citrus cinensis) waste biomass [39] and walnut hull [38].

Fig. 4.

Effect of contact time on chromium adsorption onto native and immobilized corn cob adsorbents (adsorbent dose 0.1g, Cr ions initial concentration of 100mg/L and pH (5 and 2 for Cr(III) and Cr(VI), respectively) and contact time 10–1400min).

3.4Effect of adsorbent dose

Adsorbent dosage significantly affected the Cr ions adsorption, the adsorption capacities for both types of adsorbents were higher at low adsorbent dose, which decreased as the adsorbent dosage increased (Fig. 5(A and B)). The Cr(III) adsorption was higher versus Cr(IV) for both types of corn cob adsorbents. The adsorption capacities of the native and immobilized corn cobs biomass was found higher at 0.1g dose and decreasing trend was observed at higher doses. This behavior of low adsorption at higher adsorbent dose was due to the availability of more adsorption sites at lower absorbent dose, which decreased as the dosage increased. This decreasing efficiency was due to overlapping or aggregation particle and resultantly, adsorption sites affected at higher adsorbent dose [5,6,49,55]. The enhanced adsorption capacity at low dose can be attributed to higher surface area and availability of more binding sites. Similar trend have also been reported previously for Cr ions adsorption for different adsorbents, i.e., higher adsorption at low dose, which decreased at higher dose of adsorbent at constant ions concentration and volume of solution for R. bourbonia phyto-biomass [35], sugarcane bagasse [6], T. clypeatus biomass [44], immobilized C. elegans[46] and chlorella biomass [52].

Fig. 5.

Effect of adsorbent dose on chromium adsorption onto native and immobilized corn cob adsorbents (adsorbent dose 0.1–0.5g, Cr ions initial concentration of 100mg/L and pH (5 and 2 for Cr(III) and Cr(VI), respectively) and contact time 24h).

3.5Comparison of corn cob native versus immobilized adsorbents

In comparison, the maximum adsorption capacities of immobilized corn cob were found to be 46.99mg/g for Cr(III) at pH 5 and 42.93mg/g for Cr(VI) at pH 2, for the initial metal concentration of 100mg/L, biomass dosage 0.1g and contact time 24h. The immobilized corn cob showed significantly higher adsorption efficiency versus native corn cob biomass, i.e., at different Cr ions initial concentration, contact time, pH and adsorbent dose, the immobilized corn cob efficiency was higher, however, overall adsorption trend was the same for both type of adsorbents. Earlier studies also highlighted that the immobilized biomass has more adsorption efficiency versus native biomass [6,44,46,52] and similar behavior was observed in the present investigation for native and immobilized corn cob biomass. It is well known that adsorption efficiency of adsorbent depends upon various factors like pH, temperature and adsorbent stability [49,55] and modified biomass offers more stability under variable conditions. Moreover, the surface area, [56], protonation/deprotonation, electrostatic attractions [57] and adsorbent physico-chemical properties define the activity of binding sites for effective ions entrapment, adsorption and ions retention capacity [58]. Therefore, the immobilized/modified adsorbent may offers higher adsorption capacities versus native biomass [59].

3.6Kinetics modeling

The pseudo-first order and pseudo-second order kinetics models were tested to fit the Cr adsorption experimental data. The tested pseudo-first order (Eq. (2)) and pseudo-second order (Eq. (3)) kinetics models can be seen in Eqs. (2) and (3), respectively [60,61].

where qe is the mass of metal ions adsorbed at equilibrium (mg/g), qt is the mass of metal at time t (min), k1,ads is the first order reaction rate constant of adsorption (min−1) and k2,ads is the pseudo-second order rate constant (mg/gmin−1). A comparison between pseudo-first order and pseudo-second order kinetic models is given in Table 1 for Cr(III) and Cr(VI). The pseudo-second order kinetic model with higher value of regression coefficient (R2, 0.999 and 0.999 for Cr(III) and Cr(VI), respectively) fitted well to the experimental data. The qe values (both for native and immobilized corn cob adsorbents) in case of pseudo-second order kinetic model were in agreement with experimentally determined values. From this behavior of Cr(III) and Cr(VI) ions adsorption onto immobilized and native corn cob biomass, it can be concluded that pseudo-second order kinetic explained well the Cr ions adsorption. The kinetics results were in accordance with previous studies reported for Cr by rose waste biomass [42]. While studying the adsorption of metals ions onto pretreated red rose distillation sludge [62] also reported high metal ions uptake initially followed by low adsorption and author correlated this effect with adsorption of metals ions into intracellular spaces.

Table 1.

Pseudo-first-order and pseudo-second-order kinetic models for Cr(III) and Cr(VI) adsorption onto corn cob (native and immobilized) biomasses.

Ions  Adsorbents  Pseudo first orderPseudo second order
R2  qe
Cr(III)Native corn cob  80.72  2.303×10−3  0.561  35.71  1.224×104  0.999 
Immobilized corn cob  77.45  2.308×10−3  0.731  50.01  2.44×103  0.999 
Cr(VI)Native corn cob  82.22  2.441×10−3  0.488  29.41  9.44×102  0.999 
Immobilized corn cob  77.62  2.317×10−3  0.633  45.45  2.214×103  0.999 
3.7Adsorption isotherms

The adsorption isotherms are characterized by definite parameters, whose values express the surface properties and affinity of adsorbent for metal ions adsorption [35]. In the present study, Langmuir and Freundlich isotherm models were employed and are represented in Eqs. (4) and (5), respectively [63,64].

where qe is the metal ion adsorbed (mg/g), Ce the equilibrium concentration of metal ions in solution, and KL and KF and 1/n are the Langmuir and Freundlich constants, respectively. Data fitted with Langmuir and Freundlich isotherms is given in Table 2 for Cr(III) and Cr(VI). The higher R2 and qmax values suggested that the Cr ions followed Langmuir isotherm. The Langmuir isotherm model presumes the formation of monolayer coverage of metal ions on the outer surface of adsorbent. The maximum adsorption capacity, which is a measure of the adsorption capacity to form a monolayer was found higher in case of Cr(III) as compared to Cr(VI) (Table 2). The adsorption capacity of both Cr ions were found in accordance with studies for the adsorption of Cr ions for different adsorbents i.e., rose waste biomass [42], immobilized C. elegans[46], P. ostreatus biomass [65], Chlorella biomass [52], T. clypeatus biomass [44], O. americanum seeds [53], P. crysosporium dead mass [47] and banana peel [54]. Freundlich isotherm presumes the adsorption on heterogeneous surface and is not restricted to the formation of monolayer and the fractional values of 1/n suggest the heterogeneity of adsorbent surface and simultaneously indicate a favorable adsorption of Cr(III) and Cr(VI) ions onto corn cob adsorbent. However, the values of correlation coefficients (R2) obtained in case of Freundlich isotherm model are lower than those obtained in case of Langmuir model, which indicate that the Freundlich model did not describe the adsorption of Cr(III) and Cr(VI) onto corn cob adsorbents (native and immobilized). According to Langmuir adsorption model, Cr ions adsorption occurred at homogeneous adsorption sites and intermolecular forces decreased rapidly with the distance from the adsorption surface [6,35,66]. The model further based on the assumption that all the adsorption sites are energetically identical and adsorption occurs on a structurally similar binding site.

Table 2.

Langmuir and Freundlich isotherms for Cr(III) and Cr(VI) adsorption onto corn cob (native and immobilized) biomasses.

Ions  Adsorbents  Langmuir parametersFreundlich parameters
R2  qe
1/n  R2 
Cr(III)Native corn cob  0.0039  166.66  0.942  496.00  1.651  0.699  0.999 
Immobilized corn cob  0.0047  250  0.980  567.00  2.620  0.702  0.996 
Cr(VI)Native corn cob  0.0052  111.11  0.969  105.48  1.640  0.652  0.996 
Immobilized corn cob  0.0057  166.67  0.968  112.49  2.49  0.660  0.994 
3.8Chromium adsorption from tannery wastewater

The conditions optimized for Cr ions adsorption from aqueous solution were employed for the adsorption of Cr from tannery wastewater. The wastewater sample was obtained from five local textile units, Kasur, Pakistan. For Cr(III) removal from tannery wastewater, the adsorption study was performed at pH 5, contact time 400min and adsorbent dose 0.1g, whereas for Cr(VI), pH 2.0 was adjusted and results thus obtained are shown in Fig. 6(A). Under these conditions, the Cr(III) and Cr(VI) percentage were absorbed 64.52% and 55.88% (average removal). The adsorption efficiency of immobilized was significantly higher versus native corn cob biomass for Cr ions removal from tannery wastewater, which indicates that corn cob immobilized could possibly be used for Cr sequestration from industrial effluents to avoid environmental pollution [1,67–96].

Fig. 6.

(A) Chromium ions removal from tannery effluents (sample from 5 tanneries) using corn cob immobilized adsorbent, (B) chromium adsorption for 5 repeated adsorption–desorption cycles using corn cob immobilized adsorbent and (C) chromium percentage recovery for 5 repeated adsorption–desorption cycles using corn cob immobilized adsorbent.

3.9Recycling of the adsorbent

The recycling of adsorbent is important for practical applications. The reusability/recycling of corn cob immobilized biomass was estimated by running 5 adsorption–desorption cycles. Desorption of Cr ions was performed using 0.1M NaOH solution. Cr loaded biomass was placed in contact with NaOH solution for 24 at 100rpm shaking speed and adsorption–desorption capacities recorded are shown in Fig. 6(B and C), respectively. The Cr(VI) desorption was achieved up to 86%, whereas Cr(III) was desorbed 79.8% using 0.1M NaOH. Then, adsorbent was again dried and subjected to next adsorption cycle and after 5 consecutive cycles, the adsorption capacity of corn cob immobilized adsorbent was reduced up to 0.98% for Cr(III) and 1.51% for Cr(VI), which revealed that corn cob immobilized biomass is stable and could be used for multiple adsorption cycles and NaOH was found to be efficient desorbing agent for Cr ions recovery.

3.10SEM and EDX study of corn cob biomass

EDX analysis is commonly used to determine the elemental composition of the adsorbents, through which the change in the elemental composition can be overlooked of loaded and un-loaded adsorbents. The surface morphology of the loaded and un-loaded adsorbents was performed by SEM analysis. In the present study, both EDX and SEM technique was employed to monitor the elemental composition and surface morphology of loaded and un-loaded corn cob adsorbents and responses thus obtained are shown in Fig. 7. SEM analysis clearly revealed more uniformity in loaded biomass in comparison to un-loaded biomass. It is also evident that the biomass before adsorption has an uneven surface; whereas Cr ions loaded absorbent revealed strong crosslinking on surface cell wall matrix. Further confirmation of the adsorption of Cr ions onto corn cob biomass was done by EDX analysis and results are shown in Fig. 8 of loaded and un-loaded adsorbents. The EDX pattern before adsorption did not show the characteristic signal of chromium, whereas, after adsorption a clear signal of chromium can be observed. Based on the results, it is concluded that corn cob immobilized biomass is an efficient adsorbent and can be used for metal ions adsorption from industrial effluents.

Fig. 7.

Scanning electron microscopy images of native and immobilized corn cob adsorbent; (A and B) native corn cob before adsorption, (C and D) immobilized corn cob before adsorption, (E and F) immobilized corn cob loaded with Cr(III), (G and H) immobilized corn cob loaded with Cr(VI).

Fig. 8.

EDX analysis of native and immobilized corn cob adsorbent; (A) native corn cob before adsorption, (B) immobilized corn cob biomass before adsorption, (C) immobilized corn cob after Cr(III) adsorption and (D) immobilized corn cob after Cr(VI) adsorption.


The corn cob waste biomass was immobilized in Ca–alginate matrix and adsorption efficiency was evaluated for Cr ions adsorption. At optimized conditions of Cr ions initial concentrations, pH, dosage and contact time up to 277.57mg/g and 208.6mg/L Cr(III) and Cr(VI) were adsorbed onto immobilized corn cob biomass, respectively and up to 64.52% and 55.98% Cr(III) and Cr(VI) were removed from tannery effluents. NaOH (0.1M) efficiently recovered both Cr ions and immobilized corn cob biomass showed considerable stability over five repeated adsorption–desorption cycles. Immobilization found to be a viable technique for the preparation of efficient adsorbents and could be potential adsorbents for metal ions sequestration from industrial effluents.

Conflicts of interest

The authors declare no conflicts of interest.

M. Iqbal, J. Nisar.
Cytotoxicity and mutagenicity evaluation of gamma radiation and hydrogen peroxide treated textile effluents using bioassays.
J Environ Chem Eng, 3 (2015), pp. 1912-1917
M. Mushtaq, H.N. Bhatti, M. Iqbal, S. Noreen.
Eriobotrya japonica seed biocomposite efficiency for copper adsorption: isotherms, kinetics, thermodynamic and desorption studies.
J Environ Manag, 176 (2016), pp. 21-33
R. Nadeem, Q. Manzoor, M. Iqbal, J. Nisar.
Biosorption of Pb(II) onto immobilized and native Mangifera indica waste biomass.
J Ind Eng Chem, 35 (2016), pp. 185-194
A. Rashid, H.N. Bhatti, M. Iqbal, S. Noreen.
Fungal biomass composite with bentonite efficiency for nickel and zinc adsorption: a mechanistic study.
Ecol Eng, 91 (2016), pp. 459-471
M.A. Tahir, H.N. Bhatti, M. Iqbal.
Solar red and brittle blue direct dyes adsorption onto Eucalyptus angophoroides bark: equilibrium, kinetics and thermodynamic studies.
J Environ Chem Eng, 4 (2016), pp. 2431-2439
I. Ullah, R. Nadeem, M. Iqbal, Q. Manzoor.
Biosorption of chromium onto native and immobilized sugarcane bagasse waste biomass.
Ecol Eng, 60 (2013), pp. 99-107
J. Huang, H. Yamaji, H. Fukuda.
Immobilization of Escherichia coli cells using porous support particles coated with cationic polymers.
J Biosci Bioeng, 104 (2007), pp. 98-103
T. Shishido, M. Muraoka, H. Yamaji, A. Kondo, H. Fukuda.
Production of bionanocapsules in immobilized insect cell culture using porous biomass support particles.
J Biosci Bioeng, 103 (2007), pp. 572-574
A. Tabernacka, E. Zborowska.
Trichloroethylene and tetrachloroethylene elimination from the air by means of a hybrid bioreactor with immobilized biomass.
J Biosci Bioeng, 114 (2012), pp. 318-324
H. Yamaji, S.-I. Tagai, K. Sakai, E. Izumoto, H. Fukuda.
Production of recombinant protein by baculovirus-infected insect cells in immobilized culture using porous biomass support particles.
J Biosci Bioeng, 89 (2000), pp. 12-17
Z. Zhao, X. Xie, Z. Wang, Y. Tao, X. Niu, X. Huang, et al.
Immobilization of Lactobacillus rhamnosus in mesoporous silica-based material: an efficiency continuous cell-recycle fermentation system for lactic acid production.
J Biosci Bioeng, 121 (2016), pp. 645-651
S. Amadi, C. Ukpaka.
Role of molecular diffusion in the recovery of water flood residual oil.
Chem Int, 2 (2015), pp. 103-114
A. Babarinde, K. Ogundipe, K.T. Sangosanya, B.D. Akintola, A.-O. Elizabeth Hassan.
Comparative study on the biosorption of Pb(II), Cd(II) and Zn(II) using lemon grass (Cymbopogon citratus): kinetics, isotherms and thermodynamics.
Chem Int, 2 (2016), pp. 89-102
A. Babarinde, G.O. Onyiaocha.
Equilibrium sorption of divalent metal ions onto groundnut (Arachis hypogaea) shell: kinetics, isotherm and thermodynamics.
Chem Int, 2 (2016), pp. 37-46
A. Chatterjee, L. Ray.
Biosorption of Cu(II) by immobilized biomass of Bacillus cereus M1.
J Sci Ind Res, 67 (2008), pp. 629-634
E. Eroglu, S.M. Smith, C.L. Raston.
Application of various immobilization techniques for algal bioprocesses. Biomass and biofuels from microalgae.
Springer, (2015), pp. 19-44
R. Busquets, A.E. Ivanov, L. Mbundi, S. Hörberg, O.P. Kozynchenko, P.J. Cragg, et al.
Carbon-cryogel hierarchical composites as effective and scalable filters for removal of trace organic pollutants from water.
J Environ Manag, 182 (2016), pp. 141-148
M.A. Campesi, C.D. Luzi, G.F. Barreto, O.M. Martínez.
Evaluation of an adsorption system to concentrate VOC in air streams prior to catalytic incineration.
J Environ Manag, 154 (2015), pp. 216-224
P.F. de Sales, Z.M. Magriotis, M.A.L.S. Rossi, R.F. Resende, C.A. Nunes.
Comparative analysis of tropaeolin adsorption onto raw and acid-treated kaolinite: optimization by response surface methodology.
J Environ Manag, 151 (2015), pp. 144-152
B. Li, L.Y. Li, J.R. Grace.
Adsorption and hydraulic conductivity of landfill-leachate perfluorinated compounds in bentonite barrier mixtures.
J Environ Manag, 156 (2015), pp. 236-243
Z. Liu, F. Zhang, T. Liu, N. Peng, C. Gai.
Removal of azo dye by a highly graphitized and heteroatom doped carbon derived from fish waste: adsorption equilibrium and kinetics.
J Environ Manag, 182 (2016), pp. 446-454
N. Naowanat, N. Thouchprasitchai, S. Pongstabodee.
Adsorption of emulsified oil from metalworking fluid on activated bleaching Earth-chitosan-SDS composites: optimization, kinetics, isotherms.
J Environ Manag, 169 (2016), pp. 103-115
S. Salimpour Abkenar, R.M.A. Malek, F. Mazaheri.
Dye adsorption of cotton fabric grafted with PPI dendrimers: isotherm and kinetic studies.
J Environ Manag, 163 (2015), pp. 53-61
J. Ye, X. Cong, P. Zhang, G. Zeng, E. Hoffmann, Y. Liu, et al.
Application of acid-activated Bauxsol for wastewater treatment with high phosphate concentration: characterization, adsorption optimization, and desorption behaviors.
J Environ Manag, 167 (2016), pp. 1-7
Z. Yu, L. Zhou, Y. Huang, Z. Song, W. Qiu.
Effects of a manganese oxide-modified biochar composite on adsorption of arsenic in red soil.
J Environ Manag, 163 (2015), pp. 155-162
L.P. Ramteke, P.R. Gogate.
Removal of copper and hexavalent chromium using immobilized modified sludge biomass based adsorbent.
Clean Soil Air Water, (2016),
C. Sukumar, V. Janaki, K. Vijayaraghavan, S. Kamala-Kannan, K. Shanthi.
Removal of Cr(VI) using co-immobilized activated carbon and Bacillus subtilis: fixed-bed column study.
Clean Technol Environ Pol, 19 (2016), pp. 51-58
M. Iqbal, R.A. Khera.
Adsorption of copper and lead in single and binary metal system onto Fumaria indica biomass.
Chem Int, 1 (2015), pp. 157b-163b
N.K. Benabdallah, D. Harrache, A. Mir, M. de la Guardia, F.-Z. Benhachem.
Bioaccumulation of trace metals by red alga Corallina elongata in the coast of Beni Saf, west coast, Algeria.
Chem Int, 3 (2017), pp. 220-231
S. Jafarinejad.
Control and treatment of sulfur compounds specially sulfur oxides (SOx) emissions from the petroleum industry: a review.
Chem Int, 2 (2016), pp. 242-253
S. Jafarinejad.
Recent developments in the application of sequencing batch reactor (SBR) technology for the petroleum industry wastewater treatment.
Chem Int, 3 (2017),
M.A. Jamal, M. Muneer, M. Iqbal.
Photo-degradation of monoazo dye blue 13 using advanced oxidation process.
Chem Int, 1 (2015), pp. 12-16
M. Tariq, H. Iqbal.
Maize in Pakistan – an overview.
Kasetsart J (Nat Sci), 44 (2010), pp. 757-763
B. Sultana, F. Anwar, R. Przybylski.
Antioxidant potential of corncob extracts for stabilization of corn oil subjected to microwave heating.
Food Chem, 104 (2007), pp. 997-1005
Q. Manzoor, R. Nadeem, M. Iqbal, R. Saeed, T.M. Ansari.
Organic acids pretreatment effect on Rosa bourbonia phyto-biomass for removal of Pb(II) and Cu(II) from aqueous media.
Bioresourc Technol, 132 (2013), pp. 446-452
H.N. Bhatti, I.I. Bajwa, M.A. Hanif, I.H. Bukhari.
Removal of lead and cobalt using lignocellulosic fiber derived from Citrus reticulata waste biomass.
Korean J Chem Eng, 27 (2010), pp. 218-227
G. Moussavi, B. Barikbin.
Biosorption of chromium(VI) from industrial wastewater onto pistachio hull waste biomass.
Chem Eng J, 162 (2010), pp. 893-900
X.S. Wang, Z.Z. Li, S.R. Tao.
Removal of chromium(VI) from aqueous solution using walnut hull.
J Environ Manag, 90 (2009), pp. 721-729
A.P. Marín, M. Aguilar, V. Meseguer, J. Ortuno, J. Sáez, M. Lloréns.
Biosorption of chromium(III) by orange (Citrus cinensis) waste: batch and continuous studies.
Chem Eng J, 155 (2009), pp. 199-206
M. Ajmal, R.A.K. Rao, R. Ahmad, J. Ahmad.
Adsorption studies on Citrus reticulata (fruit peel of orange): removal and recovery of Ni(II) from electroplating wastewater.
J Hazard Mater, 79 (2000), pp. 117-131
G. Annadurai, R-S. Juang, D.-J. Lee.
Use of cellulose-based wastes for adsorption of dyes from aqueous solutions.
J Hazard Mater, 92 (2002), pp. 263-274
J.M. Iqbal, F. Cecil, K. Ahmad, M. Iqbal, M. Mushtaq, M.A. Naeem, et al.
Kinetic study of Cr(III) and Cr(VI) biosorption using Rosa damascena phytomass: a rose waste biomass.
Asian J Chem, 25 (2013), pp. 2099
D. Kumar, J. Gaur.
Metal biosorption by two cyanobacterial mats in relation to pH, biomass concentration, pretreatment and reuse.
Bioresourc Technol, 102 (2011), pp. 2529-2535
L.R.S. Khowala.
Effect of pretreatment on hexavalent chromium biosorption and multimetal biosorption efficiency of Termitomyces clypeatus biomass.
Int J Integr Sci Innovat Technol, 1 (2012), pp. 7-15
C. Solisio, A. Lodi, A. Converti, M. Del Borghi.
The effect of acid pre-treatment on the biosorption of chromium(III) by Sphaerotilus natans from industrial wastewater.
Water Res, 34 (2000), pp. 3171-3178
A. Abdel-Razek.
Removal of chromium ions from liquid waste solutions using immobilized Cunninghamella elegans.
Nat Sci, 9 (2011), pp. 211-219
R. Marandi.
Biosorption of hexavalent chromium from aqueous solution by dead fungal biomass of Phanerochaete crysosporium: batch and fixed bed studies.
Can J Chem Eng Technol, 2 (2011), pp. 8-22
S. Das.
Biosorption of chromium and nickel by dried biomass of cyanobacterium Oscillatoria laete-virens.
Int J Environ Sci, 3 (2012), pp. 341-352
N. Tahir, H.N. Bhatti, M. Iqbal, S. Noreen.
Biopolymers composites with peanut hull waste biomass and application for crystal violet adsorption.
Int J Biol Macromol, 94 (2016), pp. 210-220
A. Gupta, C. Balomajumder.
Simultaneous adsorption of Cr(VI) and phenol onto tea waste biomass from binary mixture: multicomponent adsorption, thermodynamic and kinetic study.
J Environ Chem Eng, 3 (2015), pp. 785-796
S. Pandey, S.B. Mishra.
Organic–inorganic hybrid of chitosan/organoclay bionanocomposites for hexavalent chromium uptake.
J Colloid Interface Sci, 361 (2011), pp. 509-520
S. Kanchana, J. Jeyanthi, R. Dinesh Kumar.
Equilibrium and kinetic studies on biosorption of chromium(VI) on to Chlorella species.
Eur J Sci Res, 63 (2011), pp. 255-262
L. Lakshmanraj, A. Gurusamy, M. Gobinath, R. Chandramohan.
Studies on the biosorption of hexavalent chromium from aqueous solutions by using boiled mucilaginous seeds of Ocimum americanum.
J Hazard Mater, 169 (2009), pp. 1141-1145
J.R. Memon, S.Q. Memon, M.I. Bhanger, A. El-Turki, K.R. Hallam, G.C. Allen.
Banana peel: a green and economical sorbent for the selective removal of Cr(VI) from industrial wastewater.
Colloid Surf B, 70 (2009), pp. 232-237
S. Shoukat, H.N. Bhatti, M. Iqbal, S. Noreen.
Mango stone biocomposite preparation and application for crystal violet adsorption: a mechanistic study.
Microporous Mesoporous Mater, 239 (2017), pp. 180-189
A.-C. Zhang, L.-S. Sun, J. Xiang, H. Song, F. Peng, S. Su, et al.
Removal of elemental mercury from coal combustion flue gas by bentonite–chitosan and their modifier.
J Fuel Chem Technol, 37 (2009), pp. 489-495
M. Hasan, A. Ahmad, B. Hameed.
Adsorption of reactive dye onto cross-linked chitosan/oil palm ash composite beads.
Chem Eng J, 136 (2008), pp. 164-172
H.-Y. Zhu, R. Jiang, L. Xiao.
Adsorption of an anionic azo dye by chitosan/kaolin/γ-Fe2O3 composites.
Appl Clay Sci, 48 (2010), pp. 522-526
W.W. Ngah, L. Teong, M. Hanafiah.
Adsorption of dyes and heavy metal ions by chitosan composites: a review.
Carbohyd Polym, 83 (2011), pp. 1446-1456
S. Lagergren.
(1898), pp. 1-39
Y. Ho, G. McKay, D. Wase, C. Forster.
Study of the sorption of divalent metal ions on to peat.
Adsorpt Sci Technol, 18 (2000), pp. 639-650
H.N. Bhatti, R. Khalid, M.A. Hanif.
Dynamic biosorption of Zn(II) and Cu(II) using pretreated Rosa gruss an teplitz (red rose) distillation sludge.
Chem Eng J, 148 (2009), pp. 434-443
I. Langmuir.
The adsorption of gases on plane surfaces of glass, mica and platinum.
J Am Chem Soc, 40 (1918), pp. 1361-1403
H. Freundlich.
Over the adsorption in solution.
J Phys Chem, 57 (1906), pp. 1100-1107
D. Carol, S. Kingsley, S. Vincent.
Hexavalent chromium removal from aqueous solutions by Pleurotus ostreatus spent biomass.
Int J Eng Sci Technol, 4 (2012), pp. 1-7
R. Nadeem, Q. Manzoor, M. Iqbal, J. Nisar.
Biosorption of Pb(II) onto immobilized and native Mangifera indica waste biomass.
J Ind Eng Chem, 35 (2016), pp. 184-195
K. Legrouri, E. Khouya, H. Hannache, M. El Hartti, M. Ezzine, R. Naslain.
Activated carbon from molasses efficiency for Cr(VI), Pb(II) and Cu(II) adsorption: a mechanistic study.
Chem Int, 3 (2017), pp. 301-310
A.O. Majolagbe, A.A. Adeyi, O. Osibanjo.
Vulnerability assessment of groundwater pollution in the vicinity of an active dumpsite (Olusosun), Lagos, Nigeria.
Chem Int, 2 (2016), pp. 232-241
A.O. Majolagbe, A.A. Adeyi, O. Osibanjo, A.O. Adams, O.O. Ojuri.
Pollution vulnerability and health risk assessment of groundwater around an engineering Landfill in Lagos, Nigeria.
Chem Int, 3 (2017), pp. 58-68
N. Ngobiri, K. Okorosaye-Orubite.
Adsorption and corrosion inhibition characteristics of two medicinal molecules.
Chem Int, 3 (2017), pp. 185-194
K.D. Ogundipe, A. Babarinde.
Comparative study on batch equilibrium biosorption of Cd(II), Pb(II) and Zn(II) using plantain (Musa paradisiaca) flower: kinetics, isotherm, and thermodynamics.
Chem Int, 3 (2017), pp. 135-149
R. Patel, S. Kumar, A. Verma, S. Srivastava.
Kinetic and thermodynamic properties of pharmaceutical drug (Gabapentin) by potassium bromate (KBrO3) in presence of micro amount of Ir(III) chloride as catalyst in acidic medium.
Chem Int, 3 (2017), pp. 158-164
U.C. Peter, U. Chinedu.
Model prediction for constant area, variable pressure drop in orifice plate characteristics in flow system.
Chem Int, 2 (2016), pp. 80-88
K. Qureshi, M. Ahmad, I. Bhatti, M. Iqbal, A. Khan.
Cytotoxicity reduction of wastewater treated by advanced oxidation process.
Chem Int, 1 (2015), pp. 53-59
M. Sayed.
Efficient removal of phenol from aqueous solution by the pulsed high-voltage discharge process in the presence of H2O2.
Chem Int, 1 (2015), pp. 81-86
A. Shindy.
Problems and solutions in colors, dyes and pigments chemistry: a review.
Chem Int, 3 (2017), pp. 97-105
H. Shindy.
Basics in colors, dyes and pigments chemistry: a review.
Chem Int, 2 (2016), pp. 29-36
C. Ukpaka.
Development of model for bioremediation of crude oil using Moringa extract.
Chem Int, 2 (2016), pp. 19-28
C. Ukpaka.
Predictive model on the effect of restrictor on transfer function parameters on pneumatic control system.
Chem Int, 2 (2016), pp. 128-135
C. Ukpaka.
Empirical model approach for the evaluation of pH and conductivity on pollutant diffusion in soil environment.
Chem Int, 2 (2016), pp. 267-278
C. Ukpaka.
BTX degradation: the concept of microbial integration.
Chem Int, 3 (2016), pp. 8-18
C. Ukpaka, T. Izonowei.
Model prediction on the reliability of fixed bed reactor for ammonia production.
Chem Int, 3 (2017), pp. 46-57
C.P. Ukpaka, F.U. Igwe.
Modeling of the velocity profile of a bioreactor: the concept of biochemical process.
Chem Int, 3 (2017), pp. 258-267
S. Adeel, A. Ghaffar, M. Mushtaq, M. Yameen, F. Ur-Rehman, M. Zuber, et al.
Bio-processing of surface-oxidised cellulosic fibre by microwave treatment for eco-friendly textile dyeing.
Oxid Comm, 39 (2016), pp. 2396-2406
M. Iqbal.
Vicia faba bioassay for environmental toxicity monitoring: a review.
Chemosphere, 144 (2016), pp. 785-802
M. Iqbal, I.A. Bhatti.
Gamma radiation/H2O2 treatment of a nonylphenol ethoxylates: degradation, cytotoxicity, and mutagenicity evaluation.
J Hazard Mater, 299 (2015), pp. 351-360
M. Iqbal, J. Nisar, M. Adil, M. Abbas, M. Riaz, M.A. Tahir, et al.
Mutagenicity and cytotoxicity evaluation of photo-catalytically treated petroleum refinery wastewater using an array of bioassays.
Chemosphere, 168 (2017), pp. 590-598
A. Sasmaz, I.M. Dogan, M. Sasmaz.
Removal of Cr, Ni and Co in the water of chromium mining areas by using Lemna gibba L. and Lemna minor L..
Water Environ J, (2016),
M. Sasmaz, B. Akgul, D. Yıldırım, A. Sasmaz.
Bioaccumulation of thallium by the wild plants grown in soils of mining area.
Int J Phytoremediat, 17 (2016), pp. 1164-1170
M. Sasmaz, B. Akgül, D. Yıldırım, A. Sasmaz.
Mercury uptake and phytotoxicity in terrestrial plants grown naturally in the Gumuskoy (Kutahya) mining area, Turkey.
Int J Phytoremediat, 18 (2016), pp. 69-76
A. Sasmaz, E. Obek, H. Hasar.
The accumulation of heavy metals in Typha latifolia L. grown in a stream carrying secondary effluent.
Ecol Eng, 33 (2008), pp. 278-284
M. Sasmaz, E. Obek, A. Sasmaz.
Bioaccumulation of uranium and thorium by Lemna minor and Lemna gibba in Pb–Zn–Ag tailing water.
Bull Environ Contam Toxicol, (2016), pp. 1-6
M. Sasmaz, E.I.A. Topal, E. Obek, A. Sasmaz.
The potential of Lemna gibba L. and Lemna minor L. to remove Cu, Pb, Zn, and As in gallery water in a mining area in Keban, Turkey.
J Environ Manag, 163 (2015), pp. 246-253
S. Adeel, T. Gulzar, M. Azeem, M. Saeed, I. Hanif, N. Iqbal.
Appraisal of marigold flower based lutein as natural colourant for textile dyeing under the influence of gamma radiations.
Radiat Phys Chem, 130 (2017), pp. 35-39
M. Saeed, S. Adeel, M. Ilyas, M.A. Shahzad, M. Usman, E.-U. Haq, et al.
Oxidative degradation of methyl orange catalyzed by lab prepared nickel hydroxide in aqueous medium.
Desalin Water Treat, 57 (2016), pp. 12804-12813
M. Saeed, A. Haq, M. Muneer, S. Adeel, M. Hamayun, M. Ismail, et al.
Degradation of direct black 38 dye catalyzed by lab prepared nickel hydroxide in aquous medium.
Glob Nest J, 18 (2016), pp. 309-320
Copyright © 2017. Brazilian Metallurgical, Materials and Mining Association
Journal of Materials Research and Technology

Subscribe to our newsletter

Article options
Cookies policy
To improve our services and products, we use cookies (own or third parties authorized) to show advertising related to client preferences through the analyses of navigation customer behavior. Continuing navigation will be considered as acceptance of this use. You can change the settings or obtain more information by clicking here.