Journal of Chemistry

Journal of Chemistry / 2019 / Article

Research Article | Open Access

Volume 2019 |Article ID 3573704 |

Rabia Rehman, Sara Jan Muhammad, Muhammad Arshad, "Brilliant Green and Acid Orange 74 Dyes Removal from Water by Pinus roxburghii Leaves in Naturally Benign Way: An Application of Green Chemistry", Journal of Chemistry, vol. 2019, Article ID 3573704, 10 pages, 2019.

Brilliant Green and Acid Orange 74 Dyes Removal from Water by Pinus roxburghii Leaves in Naturally Benign Way: An Application of Green Chemistry

Academic Editor: Mu. Naushad
Received30 Nov 2018
Accepted07 Feb 2019
Published11 Mar 2019


The purpose of this study was to use low cost and easily accessible biosorbent for batch-scale elimination of brilliant green and acid orange 74 dyes from aqueous solution. Pinus roxburghii leaves were utilized to study their dye-eliminating capacities. The adsorbent was characterized by FTIR, TGA, DTA, and SEM. The optimized conditions for brilliant green and acid orange 74 dye elimination were adsorbent dose, 1.2 and 1.8 g; contact time, 30 and 45 min; pH, 2 and 1; temperature, 50°C and 60°C; and agitation speed, 125 rpm and 50 rpm for BG and AO-74, respectively. Adsorption records well fitted Langmuir isotherm. Possibility of the procedure was shown by negative values of the thermodynamic parameter ∆G° for both dyes. Kinetic studies showed that adsorption of BG and AO-74 dyes from watery solution by PR leaves followed pseudo-second-order kinetics.

1. Introduction

Through the increasing use of a diversity of dyes, pollution by dye wastewater is becoming a serious problem. Nearly 3000 dyes exist in the world market, and more than 6000 dyes are released in wastewater every year all over the world [1]. Textile and paper mills produce extremely colored industrial wastewater, which includes elevated BOD and floating solids that reduce the DO level for marine animals [2]. Synthetic dyes are extensively used in lots of industries [3]. Their occurrence in water is extremely lethal yet noticeable at very small concentration (1 ppm) [4]. Amongst the chemical group of dyes, azo dyes are more adaptable and account for more than half of the yearly dye manufacture [5]. It has been anticipated that, in 2003, yearly production of dyes was more than 7 × 105 metric tons [6]. Brilliant green is a synthetic organic dye. It is used in textile dying and paper printing [7]. It is very toxic if entered into the biological system. Its hazardous effects were studied in bacteria and rats [8], damaging their reproductive system and renal tissues [9]. Acid orange 74 is a monoazo acidic dye, used for textile dying. [10]. Their structures are given in Figure 1, and their properties are given in Table 1.

PropertiesBG valuesAO-74 values

ClassSynthetic organic dyeSingle azo dye
Molecular formulaC27H34N2O4SC16H12N5NaO7S
Molecular weight482.63 g/mol441.35 g/mol
Maximum absorption625 nm455 nm
SolubilitySoluble in water and alcohol with green colorSoluble in water and ethanol

A variety of techniques are used for handling wastewater such as coagulation, precipitation, photocatalytic degradation, ozonation, desalination, etc. [11], but adsorption has been set to be of better quality to other wastewater handling methods because of its low cost, simple design, easy handling property, and less susceptibility to poisonous substances [12]. This study includes batch-level elimination of BG and AO-74 dyes from aqueous solution, exploiting Pinus roxburghii leaves. They are also famous as chir pine or longleaf pine named after William Roxburgh. It is dispersed in the Himalayan districts of Bhutan, Nepal, Kashmir, Sikkim, Tibet, and India. It has numerous remedial uses. Its timber is pungent and used in tonic. It is helpful in eyeball, ear, and pharynx diseases [13]. This research work was carried out to characterize PR leaves to estimate their absorptive uniqueness for removal of BG and AO-74 dyes.

2. Experimental Work

2.1. Reagents and Instruments

Brilliant green dye (λmax: 625 nm), acid orange 74 dye (λmax: 455 nm), 0.1 M HCl, 0.1 M NaOH (Friends Laboratory Chemicals), UV/Vis spectrophotometer (UVD-3500), orbital shaker (model OSM-747), Agilent Cary 630 FTIR, and SEM (S2700 Hitachi, Japan).

2.2. Preparation of Biosorbent

PR leaves were taken from the botanical garden of Punjab University, Lahore. They were cleaned with water and dried in sunshine for 5-6 days. Afterwards, they were crushed into fine powder with an electric grinder and sieved through 40–60 mesh sieves.

2.3. Adsorption Experiment

Stock solution of dyes was made from 0.1 g of dye in a 100 mL measuring flask and diluting it up to the mark with distilled water. The standard solution (5–30 ppm) was made by diluting the stock solution. The batch experiments were performed with 100 ml of dye solutions of 30 ppm. A measured quantity (0.2 g) of adsorbent was added to the sample solution and agitated at 75 rpm for half an hour in an orbital shaker. The effect of contact time, sorbent dosage, pH, temperature, agitation speed, and initial dye concentration has been studied. Solutions were filtered from the flask at a prefixed time, and the absorbance of the filtrate was noted by using a UV/Vis spectrophotometer [14]. Adsorption percentage of dye can be calculated by using the following formula:where is the early concentration of dye and is the absorption at stability.

The amount of the coloring agent adsorbed per unit of PR leaves can be calculated with the following formula:where is the quantity of the coloring agent adsorbed by the adsorbent (mg/g), is the amount of dye solution in , and is the mass of PR leaves [15].

3. Results and Discussion

The adsorbent was characterized, and optimal state for batch-scale elimination of the colorant was established [16].

3.1. Characterization of Adsorbent

The effects of characterization of adsorbent are shown in Table 2, and FTIR spectra in Figure 2(a) had a strong peak at 3290 cm−1 that indicated the occurrence of O-H groups. Functional groups indicated by different vibrational frequencies were as follows: C-H stretching band was shown by peaks at 2918 cm−1, C=O was shown by the band at 1612 cm−1, aromatic ring was shown at 1439 cm−1, C-O aliphatic acid was indicated at 1236 cm−1 and C-O-C functionalities were indicated at 1029 cm−1. FTIR spectra of the adsorbent following color adsorption are given in Figures 2(b) and 2(c). The band of the pine leaves after dye adsorption indicated similar distinctiveness as that of the normal pine leaves apart from minute changes in the wave number of OH, C=O, and C-O-C peaks. The increase in wave number in the case of both dyes indicated that bonding of leaves might have occurred at these points [17] From Table 2, it is clear that PR leaves had 7% moisture. Bulk density and dry density were low, which showed that they are suitable material for adsorption. Porosity is the quantity for each component of the adsorbent. Porosity increases the adsorption ability of the sorbent. The iodine number confirms that it is unsaturated. The point of zero charge was three.

CharacteristicsPR leaves

Bulk density0.44
Dry density0.300
Iodine number20.17 mg/g

3.2. Effect of Adsorbent Dose

Adsorbent amount on adsorptive exclusion of BG and AO-74 dye using PR leaves as an adsorbent was calculated to be in the range of 0.2–2 g with a variation of 0.2 g. The effects are shown in Figure 3. The chart indicates relative reading of the adsorbent dosage effect of both dyes. BG and AO-74 dyes elimination increased up to a definite amount and then started decreasing to approximately stable values. Greatest % adsorption of 86.95% was obtained at 1.2 g for BG dye and 56.74% for AO-74 dye at 1.8 g. Dye exclusion effectiveness rises with rise in the adsorbent amount. But, greatest adsorption takes place when the amount is small. Active sites can be efficiently utilized when the dosage is low. When the adsorbent dose is more, less active sites are accessible, resulting in lower removal of dyes. When the process is in equilibrium, the active sites are not much inflated with the addition of more adsorbent dosage [18]. As adsorbent-adsorbent contact is more than adsorbent-adsorbate contact with increase in the sorbent amount, a minute quantity of adsorbent dosage can eradicate great quantity of dye from contaminated water [19].

3.3. Effect of Contact Time

Contact time was calculated from 15 to 90 min with a difference of 15 min. Figure 4 shows the results of the relative effect of contact time on biosorptive removal of BG and AO-74 dyes using PR leaves. It is obvious from the results that BG dye showed more percentage removal than AO-74 dye. Optimal contact time for BG was 30 min with percentage exclusion of 81.44%, and for AO-74, contact time was 45 min with percentage removal of 51.54%. Biosorptive removal of dyes improved with rise in contact time till an optimal contact time was obtained [20]. The speed of biosorptive removal is better in the initial stages of process because more adsorption sites are available. But after sometime, adsorbed dye ions repel from other unadsorbed dye ions and prevent their adsorption towards inner active sites of the biosorbent [21].

3.4. Effect of pH

pH was observed within the pH range of 1–10. Results are given in Figure 5. From the graph, it is clear that the optimal pH rate for BG was 2 with a percent removal of 90.93%, and for AO-74, the pH rate was 1 with an adsorptive removal of 55.94%. It is known that, at low pH, cationic sites of functional groups are more than anionic sites, which can chelate basic dye ions during biosorption. In the alkaline range of pH, more OH ions hinder adsorption of anionic dye due to repulsion forces. While the pH of this system is reduced, more adsorptive removal of both dyes occurs because of chelation forces [22].

3.5. Temperature Effects

Temperature is an important parameter. It affects the adsorption procedure on a huge scale. The results of temperature effects were observed in the range of 20–70°C. Figure 6 indicates that greatest removal of BG dye occurred at 50°C with a percentage removal of 94.37%. AO-74 dye gave a maximum adsorption of 17.90% at 60°C. Adsorption rises by increase in temperature. This indicates that high temperature favours this process because of its exothermic nature. It results in increase in entropy of the system, which in turn speeds up the process. Dye molecules agitate more and strike more with active binding sites at higher temperature of the solution. In addition to this fact, another reason is that inflammation of biological material at higher temperature exposes more active sites of inner sides of PR leaves. This helps more in adsorptive removal of these dyes [23].

3.6. Effect of Agitation Speed

Agitation speed was observed in the range of 25–175 rpm. From Figure 7, it is observed that optimal agitation speed for exclusion of BG dye using PR leaves was 125 rpm with adsorptive removal of 76.58%. Maximum agitation speed for AO-74 dye was 50 rpm with percent removal of 30.40%. Increase in agitation speed helps in more interaction of dye molecules with binding sites of PR leaves. Agitation is capable of reducing the external boundary sheet resistance and raises the movement of the procedure [24].

3.7. Isothermal Study

Adsorption isotherms were observed by the use of optimal state of every parameter. Mechanism of adsorption was fixed.

3.7.1. Langmuir Isotherm

Langmuir isotherm is useful for the purpose of greatest sorption ability. Linear form of representation iswhere and are called the Langmuir constants, is the equilibrium uptake ability (mg/g) of the adsorbent, is the maximum uptake ability of the adsorbent, and is the equilibrium impurity absorption in solution. From the chart, standards of these effects were calculated. is the separation factor, calculated from Langmuir constants via the following formula:

The value of shows the isotherm either to be unfavorable (RL > 1), linear (RL = 0), favorable (0 < RL < 1), or irreversible (RL < 0). The values of RL for the adsorption of both dyes onto PR leaves were less than one, which implies that the adsorption of dyes on them was a favorable procedure [25]. Correlation coefficient values R2 and qmax were higher for BG dye, which indicates that it adsorbed better than AO-74 for adsorption. Comparative graph of Langmuir isotherm is given in Figure 8, and Langmuir parameters are given in Table 3. Maximum removing capacities were compared with reported adsorbents in Table 4, and it was found that the PR leaves are very effective like other testified agrowaste materials for elimination of these toxic dyes from wastewater streams.




Adsorbents for BG dye
Modified rice straw256.41[26]
Luffa cylindrica sponge18.2[27]
Cempedak durian0.203[28]
Saklikent mud1.18[29]
Ashoka leaf powder125[30]
Psidium guajava leaves1.075[31]
Solanum tuberosum peels1.173
PR leaves71.42This study
Adsorbents for AO dye
Brown macro alga Stoechospermum marginatum35.62[33]
Spent brewery grains28.54[34]
Paulownia tomentosa Steud leaf powder10.5[35]
Azolla rongpong69.93[36]
Azolla filiculoides67.1[37]
Canola stalks25.06[38]
PR leaves7.52This study

3.7.2. Freundlich Isotherm

According to this, multilayer adsorption occurs on the outer uneven surfaces of PR leaves. Its mathematical form iswhere “” and “” are the Freundlich constants, associated to adsorption ability and adsorption strength correspondingly [39]. Relative Freundlich isotherms are shown in Figure 9, and Freundlich parameters are given in Table 5.



3.8. Thermodynamic Study

Thermodynamic behavior of adsorption of BG and AO-74 dyes onto PR leaves was calculated by the following equation:

A graph was plotted for log q/Ce and 1/T (K) × 103. The slope gives the value of ∆H°, and the intercept gives the value of ∆S [40]. Thermodynamic parameters are given in Table 6. The negative values of ΔH° and positive values of ΔS° show the exothermic temperament and arbitrariness at the solid solution boundary taking place in the interior arrangement of the adsorption correspondingly [41]. The negative value of Gibbs free energy (ΔG°) indicates a favorable and spontaneous adsorption procedure at these temperatures [42, 43].

DyesH° (kJ/mol)S° (J/mol)G° (kJ/mol)


3.9. Kinetic Study

To study the procedure of adsorption, pseudo-first-order and pseudo-second-order models were employed to check the investigational facts of adsorption tests, and the results are given in Table 7. Pseudo-first-order equation of Lagergren is written aswhere is the rate constant [44]. Linear correlation between and t shows the applicability of this model on equilibrium data. The pseudo-second-order kinetic model can be calculated by using the following formula:where is the rate constant [45]. The plot between t/q and t shows a linear relation. This kinetic model is in accordance with chemisorption being the rate-determining step. From the results, it is concluded that the pseudo-second-order model is more applicable than the first one. Elevated correlation coefficient R2 (0.992–0.995) was obtained when the second-order kinetic model was employed [46].



3.10. TGA

Three different temperature zones were observed in case of PR leaves before and after dye adsorption. As shown in Figure 10, maximum mass failure % was observed in the second zone. In the first and third zones, mass failure was relatively minute.

In case of DTA, three zones are able to study in case of normal PR leaves, BG treated leaves, AO-74 treated leaves, as given away in Figure 11. The first temperature zone is related to humidity and volatile component removal form the biosorbent. The second zone indicated further loss in weight due to pyrolysis and oxidation up to 16, 4, and 9%, respectively. At last, biosorbent mass left behind was 1, 22, and 18% after complete thermal decomposition. The residue left at this stage is dust and is about 70% of the original sample mass [47].

3.11. SEM Analysis

The scanning electron micrographs clearly revealed the face texture and morphology of untreated and dye-treated biosorbent (Figures 1214). An examination of the SEM micrograph (Figure 12) indicates the presence of many pores on the surface of the biosorbent. Figure 13 shows the surface condition on BG-treated biosorbent is somewhat swollen during the contact with dye solution. Figure 14 shows AO-74-treated biosorbent is also somewhat swollen and shows cracks on the surface [48].

3.12. Mechanism of Adsorption

The FTIR spectra of PR leaves indicated two major peaks after dye adsorption (Figure 2). After BG adsorption, the strength of the 3292 cm−1 band showing O-H stretching and the 1635 cm−1 band showing C=O stretching enhanced. It is mainly possible that intermolecular hydrogen bonding occurred between the O atom of C=O on PR leaves and the H atom of BG, or vice versa. FTIR of PR leaves with adsorbed BG indicated strong communication. It was supported by the environment of the negative charge of PR leaves and positive charge of BG. With AO-74, two major peaks shifted to 3317 and 1647 cm−1, respectively. Weak interaction in case of AO is because of negative charge for both PR leaves and AO-74 dye [49].

The mechanism of dye exclusion from aqueous solution by adsorption is understood to consist of four steps. First step is the movement of dye molecule from bulkiness of solution to the outside of adsorbent. Second step is the distribution through the border sheet to the outside of sorbent. Third step is adsorption at sites. Fourth step is intraparticle distribution into the inside of sorbent. Rate-controlling step is film distribution or pore distribution [50].

4. Conclusion

In this study, it has been obviously exposed that Pinus roxburghii leaves could be efficiently used as a low-cost adsorbent for the exclusion of dyes from aqueous solution. Maximum monolayer adsorption capacities were found to be 71.42 and 7.52 mg/g for brilliant green and acid orange 74 dyes, respectively. Adsorption process well fitted the Langmuir isotherm. Thermodynamic data showed that the adsorption procedure was impulsive and accompanied by increase in entropy. Adsorption of both dyes followed the pseudo-second-order kinetic model.


FTIR:Fourier-transform infrared spectroscopy
BG:Brilliant green
AO-74:Acid orange 74
TGA:Thermogravimetric analysis
PR:Pinus roxburghii
BOD:Biological oxygen demand
DO:Dissolved oxygen
DTA:Differential thermal analysis
SEM:Scanning electron microscope.

Data Availability

All data related to this work are presented in the Results section along with the references list.

Conflicts of Interest

The authors have no conflicts of interest regarding the publication of this paper.


The authors are thankful to University of the Punjab, Lahore, Pakistan, for funding this work.

Supplementary Materials

Graphical representation of this work. (Supplementary Materials)


  1. L. Jinqi and L. Houtian, “Degradation of azo dyes by algae,” Environmental pollution, vol. 75, no. 3, pp. 273–278, 1992. View at: Publisher Site | Google Scholar
  2. Z. Al-Qodah, “Adsorption of dyes using shale oil ash,” Water Research, vol. 34, no. 17, pp. 4295–4303, 2000. View at: Publisher Site | Google Scholar
  3. T. O’mahony, E. Guibal, and J. Tobin, “Reactive dye biosorption by Rhizopus arrhizus biomass,” Enzyme and Microbial Technology, vol. 31, no. 4, pp. 456–463, 2002. View at: Publisher Site | Google Scholar
  4. E. Forgacs, T. Cserháti, and G. Oros, “Removal of synthetic dyes from wastewaters: a review,” Environment International, vol. 30, no. 7, pp. 953–971, 2004. View at: Publisher Site | Google Scholar
  5. S. V. Mohan, N. C. Rao, K. K. Prasad, and J. Karthikeyan, “Treatment of simulated Reactive Yellow 22 (Azo) dye effluents using Spirogyra species,” Waste Management, vol. 22, no. 6, pp. 575–582, 2002. View at: Publisher Site | Google Scholar
  6. C. Fernández, M. S. Larrechi, and M. P. Callao, “An analytical overview of processes for removing organic dyes from wastewater effluents,” TrAC Trends in Analytical Chemistry, vol. 29, no. 10, pp. 1202–1211, 2010. View at: Publisher Site | Google Scholar
  7. B. K. Nandi, A. Goswami, and M. K. Purkait, “Adsorption characteristics of brilliant green dye on kaolin,” Journal of Hazardous Materials, vol. 161, no. 1, pp. 387–395, 2009. View at: Publisher Site | Google Scholar
  8. S. J. Culp and F. A. Beland, “Malachite green: a toxicological review,” Journal of the American College of Toxicology, vol. 15, no. 3, pp. 219–238, 1996. View at: Publisher Site | Google Scholar
  9. E. K. Kline, “Toxicity of brilliant green for certain bacteria,” American Journal of Public Health and the Nations Health, vol. 25, no. 3, pp. 314–318, 1935. View at: Publisher Site | Google Scholar
  10. A. Sharma and R. K. Dutta, “Studies on the drastic improvement of photocatalytic degradation of acid orange-74 dye by TPPO capped CuO nanoparticles in tandem with suitable electron capturing agents,” RSC Advances, vol. 5, no. 54, pp. 43815–43823, 2015. View at: Publisher Site | Google Scholar
  11. M. R. Awual, G. E. Eldesoky, T. Yaita et al., “Schiff based ligand containing nano-composite adsorbent for optical copper (II) ions removal from aqueous solutions,” Chemical Engineering Journal, vol. 279, pp. 639–647, 2015. View at: Publisher Site | Google Scholar
  12. V. K. Garg, R. Kumar, and R. Gupta, “Removal of malachite green dye from aqueous solution by adsorption using agro-industry waste: a case study of Prosopis cineraria,” Dyes and Pigments, vol. 62, no. 1, pp. 1–10, 2004. View at: Publisher Site | Google Scholar
  13. D. Kaushik, A. Kumar, P. Kaushik, and A. Rana, “Analgesic and anti-inflammatory activity of Pinus roxburghii sarg,” Advances in Pharmacological Sciences, vol. 2012, Article ID 245431, 6 pages, 2012. View at: Publisher Site | Google Scholar
  14. M. Naushad, T. Ahamad, B. M. Al-Maswari, A. Abdullah Alqadami, and S. M. Alshehri, “Nickel ferrite bearing nitrogen-doped mesoporous carbon as efficient adsorbent for the removal of highly toxic metal ion from aqueous medium,” Chemical Engineering Journal, vol. 330, pp. 1351–1360, 2017. View at: Publisher Site | Google Scholar
  15. S. Chowdhury and P. Saha, “Sea shell powder as a new adsorbent to remove basic green 4 (malachite green) from aqueous solutions: equilibrium, kinetic and thermodynamic studies,” Chemical Engineering Journal, vol. 164, no. 1, pp. 168–177, 2010. View at: Publisher Site | Google Scholar
  16. M. Naushad, G. Sharma, A. Kumar et al., “Efficient removal of toxic phosphate anions from aqueous environment using pectin based quaternary amino anion exchanger,” International Journal of Biological Macromolecules, vol. 106, pp. 1–10, 2018. View at: Publisher Site | Google Scholar
  17. F. Deniz, “Dye biosorption from water employing chemically modified calabrian pine cone shell as an effective biosorbent,” Environmental Progress & Sustainable Energy, vol. 34, no. 5, pp. 1267–1278, 2015. View at: Publisher Site | Google Scholar
  18. M. Naushad, S. Vasudevan, G. Sharma, A. Kumar, and Z. A. Alothman, “Adsorption kinetics, isotherms, and thermodynamic studies for Hg2+ adsorption from aqueous medium using alizarin red-S-loaded amberlite IRA-400 resin,” Desalination and Water Treatment, vol. 57, no. 39, pp. 18551–18559, 2016. View at: Publisher Site | Google Scholar
  19. V. Ponnusami, V. Gunasekar, and S. N. Srivastava, “Kinetics of methylene blue removal from aqueous solution using gulmohar (Delonix regia) plant leaf powder: multivariate regression analysis,” Journal of Hazardous Materials, vol. 169, no. 1–3, pp. 119–127, 2009. View at: Publisher Site | Google Scholar
  20. M. Naushad, A. Mittal, M. Rathore, and V. Gupta, “Ion-exchange kinetic studies for Cd(II), Co(II), Cu(II), and Pb(II) metal ions over a composite cation exchanger,” Desalination and Water Treatment, vol. 54, no. 10, pp. 2883–2890, 2015. View at: Publisher Site | Google Scholar
  21. J. Rahchamani, H. Z. Mousavi, and M. Behzad, “Adsorption of methyl violet from aqueous solution by polyacrylamide as an adsorbent: isotherm and kinetic studies,” Desalination, vol. 267, no. 2-3, pp. 256–260, 2011. View at: Publisher Site | Google Scholar
  22. M. A. Ahmad and R. Alrozi, “Removal of malachite green dye from aqueous solution using rambutan peel-based activated carbon: equilibrium, kinetic and thermodynamic studies,” Chemical Engineering Journal, vol. 171, no. 2, pp. 510–516, 2011. View at: Publisher Site | Google Scholar
  23. M. Alkan, S. Çelikçapa, Ö. Demirbaş, and M. Doğan, “Removal of reactive blue 221 and acid blue 62 anionic dyes from aqueous solutions by sepiolite,” Dyes and Pigments, vol. 65, no. 3, pp. 251–259, 2005. View at: Publisher Site | Google Scholar
  24. G. Mckay, “Adsorption of dyestuffs from aqueous solutions with activated carbon I: equilibrium and batch contact-time studies,” Journal of Chemical Technology and Biotechnology, vol. 32, no. 7–12, pp. 759–772, 2007. View at: Publisher Site | Google Scholar
  25. S. V. Mohan, S. Ramanaiah, B. Rajkumar, and P. Sarma, “Removal of fluoride from aqueous phase by biosorption onto algal biosorbent Spirogyra sp.-IO2: sorption mechanism elucidation,” Journal of Hazardous Materials, vol. 141, no. 3, pp. 465–474, 2007. View at: Publisher Site | Google Scholar
  26. R. Gong, Y. Jin, F. Chen, J. Chen, and Z. Liu, “Enhanced malachite green removal from aqueous solution by citric acid modified rice straw,” Journal of Hazardous Materials, vol. 137, no. 2, pp. 865–870, 2006. View at: Publisher Site | Google Scholar
  27. O. Segun Esan, O. Nurudeen Abiola, O. Owoyomi, C. Olumuyiwa Aboluwoye, and M. Olubunmi Osundiya, “Adsorption of brilliant green onto luffa cylindrical sponge: equilibrium, kinetics, and thermodynamic studies,” ISRN Physical Chemistry, vol. 2014, Article ID 743532, 12 pages, 2014. View at: Publisher Site | Google Scholar
  28. M. K. Dahri, L. B. Lim, and C. C. Mei, “Cempedak durian as a potential biosorbent for the removal of brilliant green dye from aqueous solution: equilibrium, thermodynamics and kinetics studies,” Environmental Monitoring and Assessment, vol. 187, no. 8, p. 546, 2015. View at: Publisher Site | Google Scholar
  29. Y. Kismir and A. Z. Aroguz, “Adsorption characteristics of the hazardous dye brilliant green on saklikent mud,” Chemical Engineering Journal, vol. 172, no. 1, pp. 199–206, 2011. View at: Publisher Site | Google Scholar
  30. N. Gupta, A. K. Kushwaha, and M. C. Chattopadhyaya, “Adsorption studies of cationic dyes onto Ashoka (Saraca asoca) leaf powder,” Journal of the Taiwan Institute of Chemical Engineers, vol. 43, no. 4, pp. 604–613, 2012. View at: Publisher Site | Google Scholar
  31. R. Rehman, T. Mahmud, and M. Irum, “Brilliant green dye elimination from water using Psidium guajava leaves and Solanum tuberosum peels as adsorbents in environmentally benign way,” Journal of Chemistry, vol. 2015, Article ID 126036, 8 pages, 2015. View at: Publisher Site | Google Scholar
  32. D. Karadag, “Modeling the mechanism, equilibrium and kinetics for the adsorption of acid orange 8 onto surfactant-modified clinoptilolite: the application of nonlinear regression analysis,” Dyes and Pigments, vol. 74, no. 3, pp. 659–664, 2007. View at: Publisher Site | Google Scholar
  33. M. Kousha, E. Daneshvar, M. S. Sohrabi, M. Jokar, and A. Bhatnagar, “Adsorption of acid orange II dye by raw and chemically modified brown macroalga Stoechospermum marginatum,” Chemical Engineering Journal, vol. 192, pp. 67–76, 2012. View at: Publisher Site | Google Scholar
  34. J. P. Silva, S. Sousa, J. Rodrigues et al., “Adsorption of acid orange 7 dye in aqueous solutions by spent brewery grains,” Separation and Purification Technology, vol. 40, no. 3, pp. 309–315, 2004. View at: Publisher Site | Google Scholar
  35. F. Deniz and S. D. Saygideger, “Equilibrium, kinetic and thermodynamic studies of acid orange 52 dye biosorption by Paulownia tomentosa steud. Leaf powder as a low-cost natural biosorbent,” Bioresource Technology, vol. 101, no. 14, pp. 5137–5143, 2010. View at: Publisher Site | Google Scholar
  36. T. V. N. Padmesh, K. Vijayaraghavan, G. Sekaran, and M. Velan, “Application of Azolla rongpong on biosorption of acid red 88, acid green 3, acid orange 7 and acid blue 15 from synthetic solutions,” Chemical Engineering Journal, vol. 122, no. 1-2, pp. 55–63, 2006. View at: Publisher Site | Google Scholar
  37. T. V. N. Padmesh, K. Vijayaraghavan, G. Sekaran, and M. Velan, “Batch and column studies on biosorption of acid dyes on fresh water macro alga Azolla filiculoides,” Journal of Hazardous Materials, vol. 125, no. 1–3, pp. 121–129, 2005. View at: Publisher Site | Google Scholar
  38. Y. Hamzeh, A. Ashori, E. Azadeh, and A. Abdulkhani, “Removal of acid orange 7 and remazol black 5 reactive dyes from aqueous solutions using a novel biosorbent,” Materials Science and Engineering: C, vol. 32, no. 6, pp. 1394–1400, 2012. View at: Publisher Site | Google Scholar
  39. A. Memon, J. Mittal, A. Malviya, and V. K. Gupta, “Removal and recovery of chrysoidine Y from aqueous solutions by waste materials,” Journal of Colloid and Interface Science, vol. 344, no. 2, pp. 497–507, 2010. View at: Publisher Site | Google Scholar
  40. M. Naushad, “Surfactant assisted nano-composite cation exchanger: development, characterization and applications for the removal of toxic Pb2+ from aqueous medium,” Chemical Engineering Journal, vol. 235, pp. 100–108, 2014. View at: Publisher Site | Google Scholar
  41. M. Naushad, T. Ahamad, G. Sharma et al., “Synthesis and characterization of a new starch/SnO2 nanocomposite for efficient adsorption of toxic Hg2+ metal ion,” Chemical Engineering Journal, vol. 300, pp. 306–316, 2016. View at: Publisher Site | Google Scholar
  42. K. Bhattacharyya and A. Sarma, “Adsorption characteristics of the dye, brilliant green, on neem leaf powder,” Dyes and Pigments, vol. 57, no. 3, pp. 211–222, 2003. View at: Publisher Site | Google Scholar
  43. S. Q. Memon, N. Memon, A. R. Solangi, and J. R. Memon, “Sawdust: a green and economical sorbent for thallium removal,” Chemical Engineering Journal, vol. 140, no. 1–3, pp. 235–240, 2008. View at: Publisher Site | Google Scholar
  44. A. A. Alqadami, M. Naushad, M. A. Abdalla et al., “Efficient removal of toxic metal ions from wastewater using a recyclable nanocomposite: a study of adsorption parameters and interaction mechanism,” Journal of Cleaner Production, vol. 156, pp. 426–436, 2017. View at: Publisher Site | Google Scholar
  45. Z. A. Al-Othman, R. Ali, and M. Naushad, “Hexavalent chromium removal from aqueous medium by activated carbon prepared from peanut shell: adsorption kinetics, equilibrium and thermodynamic studies,” Chemical Engineering Journal, vol. 184, pp. 238–247, 2012. View at: Publisher Site | Google Scholar
  46. A. Shojamoradi, H. Abolghasemi, M. Esmaili, M. Foroughi-Dahr, and H. Fatoorechi, “Experimental studies on congo red adsorption by tea waste in the presence of silica and Fe2O3 nanoparticles,” Journal of Petroleum Science and Technology, vol. 3, no. 2, pp. 25–34, 2013. View at: Google Scholar
  47. I. D. Mall, V. C. Srivastava, and N. K. Agarwal, “removal of orange-G and methyl violet dyes by adsorption onto bagasse fly ash-kinetic study and equilibrium isotherm analyses,” Dyes and Pigments, vol. 69, no. 3, pp. 210–223, 2006. View at: Publisher Site | Google Scholar
  48. Y. Vijaya, S. R. Popuri, V. M. Boddu, and A. Krishnaiah, “Modified chitosan and calcium alginate biopolymer sorbents for removal of nickel (II) through adsorption,” Carbohydrate polymers, vol. 72, no. 2, pp. 261–271, 2008. View at: Publisher Site | Google Scholar
  49. Y. Qiu, Z. Zheng, Z. Zhou, and G. D. Sheng, “Effectiveness and mechanisms of dye adsorption on a straw-based biochar,” Bioresource Technology, vol. 100, no. 21, pp. 5348–5351, 2009. View at: Publisher Site | Google Scholar
  50. T. K. Sen, S. Afroze, and H. M. Ang, “Equilibrium, kinetics and mechanism of removal of methylene blue from aqueous solution by adsorption onto pine cone biomass of Pinus radiata,” Water, Air, & Soil Pollution, vol. 218, no. 1–4, pp. 499–515, 2011. View at: Publisher Site | Google Scholar

Copyright © 2019 Rabia Rehman et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Related articles

No related content is available yet for this article.
 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

No related content is available yet for this article.

Article of the Year Award: Outstanding research contributions of 2021, as selected by our Chief Editors. Read the winning articles.