| Home | E-Submission | Sitemap | Contact Us |  
Environ Eng Res > Volume 21(2); 2016 > Article
Thanhmingliana, Lalhriatpuia, Tiwari, and Lee: Efficient removal of 17β-estradiol using hybrid clay materials: Batch and column studies

Abstract

Hybrid materials were obtained modifying the bentonite (BC) and local clay (LC) using hexadecyltrimethylammonium bromide (HDTMA) or the clay were pillared with aluminum followed by modification with HDTMA. The materials were characterized by the SEM, FT-IR and XRD analytical tools. The batch reactor data implied that the uptake of 17β-estradiol (E2) by the hybrid materials showed very high uptake at the neutral pH region. However, at higher and lower pH conditions, slightly less uptake of E2 was occurred. The uptake of E2 was insignificantly affected changing the sorptive concentration from 1.0 to 10.0 mg/L and the background electrolyte (NaCl) concentrations from 0.0001 to 0.1 mol/L. Moreover, the sorption of E2 by these hybrid materials was fairly efficient since within 30 mins of contact time, an apparent equilibrium between solid and solution was achieved, and the data was best fitted to the PSO (pseudo-second order) and FL-PSO (Fractal-like-pseudo second order) kinetic models compared to the PFO (pseudo-first order) model. The fixed-bed column results showed that relatively high breakthrough volume was obtained for the attenuation of E2 using these hybrid materials, and the loading capacity of E2 was estimated to be 75.984, 63.757, 58.965 and 49.746 mg/g for the solids BCH, BCAH, LCH and LCAH, respectively.

1. Introduction

Micro-pollutants in the aquatic environment pose serious environmental concerns because of their persistency and toxicity towards living organisms. There are several natural and synthetic chemicals that show endocrine disruption and cause interference in the reproduction and development of aquatic organisms [1]. 17β-Estradiol (E2) is one of the most potent forms of natural estrogen and is identified as a potential water pollutant among several endocrine disrupting chemicals (EDCs). This is because it triggers greatly the negative responses in aquatic organisms even at very low concentrations [2]. It is often found in surface and subsurface aquatic environment [3]. Human and animal urine and feces as in the form of free estrogens or as glucuronide and/or sulfate conjugates are the major sources of these pollutants into the aquatic environment. Although these steroid conjugates do not show affinity to estrogen receptors, however, these are converted into deconjugated forms by chemical or enzymatic means in sewage treatment plants, and hence are considered as potential and emerging sources of active estrogens which lead to adverse reproductive effects on ecosystems [4].
The effect of these hormones on human health at environmentally relevant concentrations is, of course, unclear. However, the effect of E2 on non-target organisms, including endocrine disruption is affecting sexual development and reproduction [56]. The formation of female specific vitellogenin was reported in male rainbow trout when exposed to E2 concentration as low as 1 ng/L [7]. Similarly, the exposure of male Japanese medaka to 10 ng/L E2 was induced the production of female-specific proteins, resulted the formation of intersex (ova in the testes) and altered sex species [8]. Therefore, an efficient and cost effective treatment processes need to be developed in order to fine tune the existing wastewater treatment plants. Sorptive removal using variety of newer materials is one of possible options for decontaminating the aquatic environment contaminated with steroidal estrogens. In fact, a number of sorbent materials have been applied for eliminating E2 including surface soils [6], granular activated carbon (GAC), chitin, chitosan, ion exchange resin, carbonaceous adsorbent prepared from industrial waste [9], natural sediments [10], bone char [11], powdered activated carbons [12], single-walled carbon nanotubes [13], multi-walled carbon nanotubes [14] polyamide thin-film composite nanofiltration (NF) membranes [15], and molecularly imprinted polymer [16]. However, these sorbents suffer the problem of either low sorption capacities or seemingly high-cost of materials. Thus, there need to search a high-performance and low-cost adsorbent for an efficient removal of micro-pollutants from aqueous environments.
The applications of porous pristine clays in the remediation of aquatic environment was often employed however, the removal capacities of pristine clay was reportedly low towards several hydrophobic impurities. Therefore, the modified clay materials were intended to employ in the selective and specific removal of micro-pollutants from aqueous solutions. The introduction of cationic surfactant within inter lamellar space through the ion exchange process caused significantly the chemical properties of clay minerals. This apparently enhances the hydrophobic/organophilic character of clay and the modified clays are likely to be effective/efficient towards the organic pollutants attenuation [17]. Similarly, the hybrid materials obtained by pillaring with poly(hydroxo-metal) cations and simultaneous intercalation of suitable organic cations showed an enhanced applicability in wastewater treatment since this showed fairly high affinity towards the organic impurities, and also possessed with achievable settling capacity which enabled it easy for phase separation [18].
Therefore, the present study aims to obtain and employ the hybrid materials, precursor to the natural bentonite or locally collected clay in an attempt to attenuate E2 efficiently and effectively from aquatic environments. Further, the batch reactor operations are conducted in a wide range of chemical parametric studies which provides a plausible mechanism involved at the solid/solution interface, along with the fixed-bed column reactor operations to optimize the loading capacity of E2 under the dynamic conditions.

2. Materials and Methods

2.1. Materials

Local clay was collected from the field of Phullen, Mizoram (India). It possessed with several impurities hence; it was thoroughly separated using the ISRIC (International Soil Reference and Information Centre) standard method as detailed elsewhere [19]. However, the bentonite clay (BC) was procured from a commercial supplier and was used after simple washing with distilled water and dried at 90°C in a drying oven. The two clay samples were crushed in a mortar and sieved to obtain 100 BSS (British Standard Sieve) mesh size particles. The cation exchange capacity (CEC) of pristine clay was determined by the US EPA (United States Environmental Protection Agency) method 9080 [20]. The CEC of BC and LC were found to be 69.35 and 46.38 meq/100 g of clay, respectively. Aluminium (III) chloride was obtained from Merck, India. Hexadecyltrimethylammonium bromide (HDTMA) and 17b-Estradiol (E2) were procured from Sigma-Aldrich, USA. Sodium chloride, Extrapure was obtained from HiMedia, India. Water purified with a Millipore water purification system (Milli–Q+) was used throughout the whole experiment.
/upload/thumbnails/eer-21-2-203i1.gif

2.2. Methods

2.2.1. Preparation of organoclay and inorgano–organoclay

BC or LC was modified by the usual wet cation exchange process as described earlier [21]. In brief, 20 g of each clay powder was added separately into 1 L of HDTMA solution to saturate 100% of the respective clay CEC. The slurry was refluxed for 48 h at 60°C under constant stirring. It was filtered and the solid was washed several times with purified water. Excess or free surfactant was removed with Soxhlet extraction. The organo-modified bentonite/or local clay was dried at 90°C in a drying oven and then stored in an airtight polyethylene bottle. The HDTMA-modified BC and LC were then labeled as BCH and LCH respectively.
The bentonite and/or local clay was pillared with aluminium and then modified with organic cations HDTMA as to obtain the HDTMA-Al-bentonite (BCAH) or HDTMA-Al-local clay (LCAH) materials. In brief, aluminium(III) solution was prepared by mixing 100 mL of 0.4 mol/L NaOH and 100 mL of 0.2 mol/L aluminium(III) chloride solutions under vigorous and constant stirring. The solution mixture was kept for 7 days for ageing at room temperature. Further, in this aluminium solution a known amount of HDTMA (to saturate 100% of the clay CEC) was added under stirred conditions. BC or LC clay powders (4 g) each in 300 mL of water was then taken in round bottom flask. To this solution mixture, HDTMA-aluminium solution was added and stirred for Ca. 5 h at room temperature. The slurry was then kept at room temperature for another 2 days. The modified clay was separated carefully and the solid was washed with plenty of distilled water as to obtain materials free from the halides or any unbound/free HDTMA. These solids were then dried at 50°C in a drying oven and grounded gently in a mortar. The AL-HDTMA-modified BC and LC were then labeled as BCAH or LCAH, respectively.

2.2.2. Characterization of materials

The surface morphology of the hybrid materials and the pristine clay was obtained using the FE-SEM (Field Emission Scanning Electron Microscope: Model S-4700, Hitachi, Japan) images. X-ray diffraction (XRD) data were collected using an X-ray diffraction machine (PANalytical, Netherland; Model X’Pert PRO MPD), employing Cu-Kα radiations having the wavelength of 1.5418 Å. FT-IR (Fourier Transform-Infra Red) data was obtained with a FT-IR machine (Bruker, Tensor 27, USA using KBR disk method). The point of zero charge (pHPZC) of these materials was determined by the batch pH drift method as detailed elsewhere [22].

2.2.3. Batch reactor experiments

A stock solution (10.0 mg/L) of E2 was prepared by dissolving an appropriate amount of E2 in purified water at elevated pH with dilute NaOH. Further, the required E2 concentration was obtained by dilution of the stock solution and the pH was adjusted with the dropwise addition of 0.1 mol/L HCl. The pH dependence sorption experiment was carried out by taking a series of 5.0 mg/L of E2 solution (50 mL) into polyethylene bottles and the pH was adjusted by drop wise addition of 0.1 mol/L HCl or NaOH solutions. 0.1 g of the solid sample was introduced into these sorptive solutions. The bottles were kept in an automatic incubator shaker (Incubator Shaker, TM Weiber, ACMAS Technologies Pvt. Ltd., India) for 24 hours at 25 ± 1°C. The bottles were then taken out from the shaker and the solution mixture was filtered with 0.45 μm syringe filter. The pH was again checked and reported as equilibrium pH. Absorbance of the filtrates was measured using UV-Visible Spectrophotometer (Model: UV1, Thermo Electron Corporation, USA). The absorbance was recorded at 280 nm. Calibration curve was obtained using standard E2 solutions having varied concentrations. Results were presented as percent E2 removal as a function of equilibrium pH. The blank E2 (5.0 mg/L) solutions were shaken without the hybrid materials in the polyethylene bottles for 24 h. The samples were filtered with a 0.45 mm syringe filter and their absorbance was determined at the same wavelength of 280 nm. No decrease in absorbance was observed, which indicated that negligible sorption of E2 was occurred to the polyethylene bottles.
The concentration dependence data was collected by varying the E2 concentrations from 1.0 to 10.0 mg/L at constant pH~7.0 and at constant temperature (25 ± 1°C). Results were presented as percent E2 removal as a function of initial E2 concentration (mg/L). Time dependence sorption of E2 by these hybrid materials was obtained at different time intervals of contact. Initial E2 concentration 5.0 mg/L with a solid dose of 2.0 g/L was taken as constant and the sorption experiments were conducted at constant pH ~7.0 and temperature 25 ± 1°C. Results were then reported as percent E2 removal as a function of time (min.). Effect of background electrolyte concentration on the sorption of E2 was studied varying the NaCl concentration from 0.0001 to 0.1 mol/L with E2 concentration of 5.0 mg/L. The solution pH (~7.0) and temperature (25 ± 1°C) was kept constant throughout the experiments. Results were again presented as percent E2 removal as a function of background electrolyte (NaCl) concentrations.

2.2.4. Fixed-bed column experiments

Fixed-bed column experiments were conducted using a glass column (1 cm inner diameter). 0.25 g of hybrid materials was kept in the middle of the column. Below and above the hybrid material, 1.0 g of sand (14–16 BSS) was placed and the rest of the column was packed with glass beads. E2 (5.0 mg/L) solution at pH ~7.0 was pumped up from the bottom of the column using a peristaltic pump (KrosFlo Research I Peristaltic Pump, Spectrum Laboratories Inc., California, USA), at a constant flow rate of 1.0 mL/min. Effluent solution was collected using a fraction collector (Spectra/Chrom CF-2 Fraction Collector, Spectrum Laboratories Inc., California, USA). The collected effluents were filtered with 0.45 μm syringe filter and absorbance of the filtrate was measured with UV-Vis Spectrophotometer.
Column breakthrough data obtained were utilized to optimize the loading capacity of E2 by the materials under the dynamic conditions employing Thomas equation [23]:
(1)
CeCo=11+e(KT(qom-CoV))/Q
where Ce and Co are the concentrations (mg/L) of effluent and influent solutions of E2, respectively; KT refer to the Thomas rate constant (L/min/mg); qo is the maximum amount (mg/g) of E2 loaded under the specified column conditions; ‘m’ is the mass (g) of hybrid materials taken in the column; V is the throughput volume (L); and Q is the flow rate (L/min) of pumped E2 solution. The column data were fitted to a non-linear Thomas equation using the least square fitting method to estimate the two unknown parameters, KT and qo.

3. Results and Discussion

3.1. Characterization of Materials

FT-IR data indicated that the hybrid materials, viz., BCH, BCAH, LCH or LCAH were possessed with prominent IR stretching bands at around the wave numbers 2930 cm−1 and 2850 cm−1 which were due to the –CH2 asymmetric and symmetric stretching vibrations, respectively (Fig. S1). This confirmed the introduction of HDTMA molecule within the clay network with these hybrid materials. Bentonite and local clay XRD data was matched with the standard ICDD (International Centre for Diffraction Data) reference pattern. It was noted that both the clay samples contained with quartz, smectite, illite and kaolinite minerals with varied percent composition as characteristic peaks were assigned in the XRD diffraction pattern. Further, quantitatively, the bentonite was having 43.71%, 23.17%, 1.73% and 31.39% of quartz, smectite, kaolinite and illite, respectively. Similarly, local clay was contained with 79.35%, 6.20%, 0.45% and 14.01%, respectively of quartz, smectite, kaolinite and illite. The XRD patterns of the modified clay samples were almost identical to the pristine clay, with a slight change in d-values and intensities of the peaks (Fig. S2). The FE-SEM images clearly show that the organo-modified clay (i.e., BCH or LCH) solids possessed more heterogeneous surface structures compared to the pristine clays (Fig. S3). BCAH and LCAH solids also possessed similar heterogeneous surface structure, although they contained with newly aggregated particles onto the surface which were possibly the immobilized aluminium hydroxide or Al2O3 molecules. Detailed characterizations of these materials were described previously [21].
The BET specific surface area, pore volume and pore size of these solids, viz., BC, BCH, BCAH, LC, LCH and LCAH were obtained by the nitrogen adsorption and desorption method and results were returned in Table 1. It was observed that BC was having very high value of the BET specific surface area, with low pore volume and pore size. The high specific surface area of BC was due to the high percentage of smectite, kaolinite and illite mineral phases compared to the quartz/silica content. However, the HDTMA- or Al-HDTMA-modified bentonite materials were showed a remarkable decrease in specific surface area and an increased in pore size (diameter) and pore volume of the materials. It was due to the fact that the HDTMA or aluminium were occupied the interspace of clay and caused to decrease the specific surface area of clay, whereas the propping up of the interlayer was caused to enhance the pore size and pore volume of the solids. On the other hand, the unmodified local clay (LC) showed very significantly low specific surface area, possibly, due to the compact surface structure of LC which contained dominantly with the silica/quartz. However, the presence of HDTMA or Al-HDTMA caused to increase slightly the specific surface area of solids with a decrease in pore diameter of the modified solids.

3.2. Batch Reactor Operations

3.2.1. Effect of pH

The pH dependence removal of E2 (pH 4.02 to 10.13) by these solids was presented graphically in Fig. 1. It was observed that a very high uptake of E2 was achieved within the studied pH region. It was further recorded that a slight decrease in sorption of E2 was observed at very low and high pH values. The uptake of E2 by these solids could be ascribed with the help of speciation of E2 as well the surface properties of the solids. E2 is having the acid dissociation constant (pKa) of 10.23 [14], which indicated that E2 exists as a neutral molecule almost up to pH ~10.2 and carries a net negative charge above this pH value. On the other hand, the pHPZC value of these solids was found to be 9.8, 8.2, 6.1, 5.8, 5.1 and 5.1 for the samples BC, BCH, BCAH, LC, LCH and LCAH respectively. This implied that except BC and BCH solid, other materials possessed a net negative charge at and around neutral pH. Therefore, the possibility of electrostatic attraction of E2 by the solid surface was, perhaps, ruled out. Hence, the possible interaction of E2 with the solid surface was due to the hydrophobic or organophilic nature of the hybrid materials. The mechanism of E2 uptake by these hybrid materials is therefore, assumed primarily with the fact that the introduction of organic cation (HDTMA) within the clay network caused to enhance the hydrophobicity or organophilic nature of the surface. This enabled E2 to partition at the introduced hydrophobic core. On the other hand; LCAH solid showed slightly less uptake of E2, possibly, due to the screening of the introduced HDTMA molecule in presence of aluminium oxide/hydroxide particles onto the solid surface. Hence, this caused to reduce the hydrophobic core within the clay network. Further, the removal of E2 was decreased to some extent with increasing the solution pH to10.0. This is due to the partial acidic dissociation of E2. This caused, to some extent, for electrostatic repulsion and hence was reduced in partitioning of E2 within the hydrophobic core of the hybrid materials. It was reported previously that the organoclays prepared with longer chain surfactant molecule were less influenced by the solution pH [24]. Moreover, the hybrid materials precursor to natural sericite and modified with HDTMA and alkyldimethylbenzylammonium chloride were used in the remediation of wastewaters contaminated with BPA, and the increased in pH from ca. 2.0 to 10.0 did not significantly affect the percentage uptake of BPA by these hybrid materials [22]. It was also noted that the virgin bentonite and local clay showed very insignificant or significantly less uptake of E2 (ca. 42.86% and 37.14% at pH 7.21 and 7.16 for BC and LC, respectively), which was further decreased at low and high pH conditions. The sorption of E2 by all these hybrid materials, compared to the unmodified clays, show significantly enhanced percent uptake and enhanced the applicability of hybrid materials at least in the remediation of water contaminated with E2 pollutant.

3.2.2. Effect of E2 concentration

The effect of initial sorptive concentration is one of the effective factors in estimating the sorption efficiency/capacity. The sorption of E2 was obtained as a function of initial sorptive concentrations and was presented in Fig. 2(a). The figure revealed that increasing the initial concentration of E2 from Ca. 1.0 to 10.0 mg/L, a very high percent uptake was not significantly affected with this increase in sorptive concentration (cf. Fig. 2(a)) However, on the other hand, the amount of E2 removal was increased significantly, increasing the initial E2 concentration (Fig. 2(b)). These results again indicated the strong affinity of E2 towards the hybrid materials and an effective attenuation of E2 was obtained.

3.2.3. Effect of background electrolyte concentration

Effect of background electrolytes in the sorptive removal of E2 by the hybrid materials could help to explain the mechanism involved at solid/solution interface. The specific sorption is usually not much influenced by the change in background electrolyte concentrations; whereas the non-specific sorption is greatly influenced by the change in background electrolyte concentrations [25]. The percent removal of E2 as a function of background electrolyte (NaCl) concentrations is shown graphically in Fig. 3. The results indicated that increasing the background electrolyte concentrations from 0.0001 to 0.1 mol/L NaCl (i.e., 1000 times increase) was not significantly affected the percent uptake of E2 by the hybrid materials, i.e., BCH, BCAH, LCH and LCAH. This indicated again the strong affinity of solids towards E2. This implied that the partitioned E2 was bound with relatively stronger van der Waals forces which retained firmly the E2 molecule onto or within the interspace of hybrid materials. Previously, it was reported that the increase in NaCl concentration from 0 to 320 mm did not significantly change the adsorption of 17 α-ethinylestradiol (EE2) from landfill leachate onto single-walled carbon nanotubes (SWCNTs) [26]. Also the uptake of As(V) was almost unaffected by the 1000 times increase in background electrolyte concentration, using manganese coated activated carbon samples. It was further stated that As(V) were specifically sorbed onto the solid surface and predominantly formed ‘inner-sphere complexes’ onto the solid surface [27].

3.2.4. Time dependence removal

The percent of E2 removed as a function of time was plotted in Fig. 4. It was evident from the fig. that the materials were efficient in the removal of E2 from aqueous solutions since within initial 10–15 min of contact, a maximum E2 were aggregated onto the solid surface and was resulted in maximum percent uptake of E2. This was then gradually slowed down and an apparent equilibrium was achieved within ca. 30 min of contact. This again reaffirmed the affinity of these solids towards E2. Also it was again noted that the uptake of E2 onto the LCAH solid was slightly lesser than the other hybrid materials.
The time dependence sorption data was then utilized to perform the kinetic modelling. The non-linear form of three different kinetic models, viz., pseudo-first order (PFO) [28], pseudo-second order (PSO) [29] and fractal-like pseudo-second order (FL-PSO) [30] models (Eq. (2)(4)) were utilized:
(2)
qt=qe(1-exp(-k1t))
(3)
qt=k2qe2t1+k2qet
(4)
qt=kqe2tα1+kqetα
where qt and qe are the amount of E2 removed at time ‘t’ and removal capacity at equilibrium, respectively. k1 and k2 are the pseudo-first and pseudo-second order rate constants, respectively. Similarly, the constants k and a are referred to the rate constant and fractal constant, respectively. A non-linear least square fitting was conducted and the unknown parameters were optimized. The estimated values of the unknown parameters along with the least square sum were then returned in Table 2. The simulation data was best fitted to the PSO and FL-PSO kinetic models compared to the PFO model since reasonably a low value of least square sum was obtained for these two models. Further, a fair applicability of the PSO or FL-PSO models pointed that the E2 species were bound onto the surface of these hybrid materials with relatively a strong forces. Previously, Patel et al. [11] reported that the adsorption of E2 on bone char obeyed the pseudo second-order kinetic model and they assumed that chemisorption mechanism was involved in the adsorption process. Similar result was obtained in the sorptive removal of bisphenol A by some of the hybrid materials precursor to the natural sericite [22].

3.2.5. Fixed-bed column reactor operations

Fixed-bed column reactor studies were performed to assess the loading capacity of the hybrid materials, viz., BCH, BCAH, LCH and LCAH for E2 under the dynamic conditions. The column experiments were conducted with the stated column conditions. The breakthrough curves obtained were presented graphically in Fig. 5. Figure revealed that relatively high breakthrough volume was obtained for E2 by these solids. A complete breakthrough was obtained at the throughput volume of 6.18, 5.40, 4.92 and 4.26; respectively for the BCH, BCAH, LCH and LCAH solids. Relatively high value of breakthrough volume indicated the high removal capacity of E2 by the modified solids under the dynamic conditions as well. This further showed that the modified solids could be potential and promising sorbing materials for the effective attenuation of E2 from aqueous solutions.
Further, the non-linear least square fitting was conducted with the breakthrough column data using the Thomas equation (Eq. (1)). The fitting was performed to simulate the two unknown parameters, i.e., KT and qo. The values of Thomas constants along with the least square sum were estimated and returned in Table 3. These results indicated that a high loading capacity was achieved for E2 by these solids under the dynamic conditions. Relatively, BCH showed higher removal capacity for E2 compared to the BCAH solid. Similarly, LCH solid possessed relatively higher removal capacity than LCAH solid. The removal capacity followed the trend: BCH > BCAH > LCH > LCAH. These results were similar to the findings of batch reactor experiments. Also, the results were in a line to other reports in which the Thomas equation was utilized to demonstrate the loading capacity of different sorbing materials [18, 31].

4. Conclusions

Organo-modified clay and inorgano-organo-modified clay materials, precursor to the natural bentonite and local clay were obtained and efficiently used in the removal of E2 from aqueous solutions. The batch sorption data implied that the high uptake of E2 by the hybrid materials was slightly affected at low and high pH values. The uptake was insignificantly affected by the change in the sorptive concentration (i.e., from 1.0 mg/L to 10.0 mg/L) and the background electrolyte concentration (0.0001 to 0.1 mol/L NaCl). Moreover, the attenuation of E2 by these hybrid materials was fairly efficient as within 30 min of contact time, an apparent equilibrium between the solid and solution was achieved, and the data was best fitted to the PSO and FL-PSO kinetic models compared to the PFO model. The fixed-bed column results showed that relatively high breakthrough volume were obtained for attenuation of E2 using the hybrid materials, and the loading capacity of E2 was estimated to be 75.984, 63.757, 58.965 and 49.746 mg/g for the solids BCH, BCAH, LCH and LCAH, respectively. These results, in brief, indicated that the hybrid materials possessed potential application in the remediation of aquatic environment contaminated with the E2.

SUPPLEMENTARY MATERIAL

Acknowledgments

One of the Author Thanhmingliana wishes to the UGC, New Delhi for financial support as in the form of UGC (NERO) minor project (vide No. F.5-22/2013-14/(MRP/NERO)/261). Also, DT acknowledges the CSIR, New Delhi for partial support as a Major Project (vide No.: 01 (2567)/12/EMR-II).

References

1. Evgenidou EN, Konstantinou IK, Lambropoulou DAOccurrence and removal of transformation products of PPCPs and illicit drugs in wastewaters: A review. Sci Total Environ. 2015;505:905–926.
crossref

2. Jiang L, Liu Y, Zeng G, et alRemoval of 17β-estradiol by few-layered graphene oxide nanosheets from aqueous solutions: External influence and adsorption mechanism. Chem Eng J. 2016;284:93–102.
crossref

3. Bai X, Casey FXM, Hakk H, DeSutter TM, Oduor PG, Khan ESorption and degradation of 17β-estradiol-17-sulfate in sterilized soil–water systems. Chemosphere. 2015;119:1322–1328.
crossref

4. Lee JH, Zhou JL, Kim SDEffects of biodegradation and sorption by humic acid on the estrogenicity of 17β-estradiol. Chemosphere. 2011;85:1383–1389.
crossref

5. Hanselman TA, Graetz DA, Wilkie ACManure-borne estrogens as potential environmental contaminants: a review. Environ Sci Technol. 2003;37:5471–5478.
crossref

6. Mashtare ML, Khan B, Lee LSEvaluating stereoselective sorption by soils of 17α-estradiol and 17β-estradiol. Chemosphere. 2011;82:847–852.
crossref

7. Hansen PD, Dizer H, Hock B, et alVitellogenin- a biomarker for endocrine disruptors. Trac Trend Anal Chem. 1998;17:448–451.
crossref

8. Metcalfe CD, Metcalfe TL, Kiparissis Y, et alEstrogenic potency of chemicals detected in sewage treatment plant effluents as determined by in vivo assays with Japanese medaka (Oryzias latipes). Environ Toxicol Chem. 2001;20:297–308.
crossref

9. Zhang Y, Zhou JLRemoval of estrone and 17β-estradiol from water by adsorption. Wat Res. 2005;39:3991–4003.
crossref

10. Sangster JL, Oke H, Zhang Y, Bartelt-Hunt SLThe effect of particle size on sorption of estrogens, androgens and progestagens in aquatic sediment. J Hazard Mater. 2015;299:112–121.
crossref

11. Patel S, Han J, Gao WSorption of 17β-estradiol from aqueous solutions on to bone char derived from waste cattle bones: Kinetics and isotherms. J Environ Chem Eng. 2015;3:1562–1569.
crossref

12. Yoon Y, Westerhoff P, Snyder SA, Esparza MHPLC-fluorescence detection and adsorption of bisphenol A, 17β-estradiol, and 17α-ethynyl estradiol on powdered activated carbon. Wat Res. 2003;37:3530–3537.
crossref

13. Zaib Q, Khan IA, Saleh NB, Flora JRV, Park YG, Yoon YRemoval of bisphenol A and 17β-estradiol by single-walled carbon nanotubes in aqueous solution: adsorption and molecular modeling. Wat Air Soil Pollut. 2012;223:281–3293.


14. Sun W, Zhou KAdsorption of 17β-estradiol by multi-walled carbon nanotubes in natural waters with or without aquatic colloids. Chem Eng J. 2014;258:185–193.
crossref

15. McCallum EA, Hyung H, Do TA, Huang CH, Kim JHAdsorption, desorption, and steady-state removal of 17β-estradiol by nanofiltration membranes. J Membr Sci. 2008;319:38–43.
crossref

16. Le Noir M, Lepeuple AS, Guieysse B, Mattiasson BSelective removal of 17β-estradiol at trace concentration using a molecularly imprinted polymer. Wat Res. 2007;41:2825–2831.
crossref

17. Lee SM, Tiwari DOrgano and inorgano-organo-modified clays in the remediation of aqueous solutions: An overview. Appl Clay Sci. 2012;59–60:84–102.
crossref

18. Thanhmingliana , Lee SM, Tiwari D, Prasad SKEfficient attenuation of 17a-ethynylestradiol (EE2) and tetracycline using novel hybrid materials: batch and column reactor studies. RSC Adv. 2015;5:46834–46842.
crossref

19. ISRIC. Procedures for soil analysis [Internet]. Reeuwijk: ISRIC; c2002. Available from: http://www.isric.org/isric/webdocs/docs/ISRIC_TechPap09_2002.pdf2002.


20. EPA. 1986. Method 9080, Cation-exchange capacity of soils (ammonium acetate) [Internet]. Available from: www3.epa.gov/epawaste/hazard/testmethods/sw846/pdfs/9080.pdf


21. Thanhmingliana , Tiwari DEfficient use of hybrid materials in the remediation of aquatic environment contaminated with micro-pollutant diclofenac sodium. Chem Eng J. 2015;263:364–373.
crossref

22. Thanhmingliana , Lee SM, Tiwari DUse of hybrid materials in the decontamination of bisphenol A from aqueous solutions. RSC Adv. 2014;4:43921–43930.


23. Thomas HCHeterogeneous ion exchange in a flowing system. J Am Chem Soc. 1944;66:1664–1666.
crossref

24. Park Y, Ayoko GA, Kurdi R, Horváth E, Kristóf J, Frost RLAdsorption of phenolic compounds by organoclays: Implications for the removal of organic pollutants from aqueous media. J Colloid Interf Sci. 2013;406:196–208.
crossref

25. Lalhmunsiama , Gupta PL, Pawar RR, Lee SMUse of algal biomass in the remediation of aqueous waste contaminated with cadmium. Sci Technol J. 2015;3:14–20.


26. Joseph L, Zaib Q, Khan IA, et alRemoval of bisphenol A and 17α-ethinylestradiol from landfill leachate using single-walled carbon nanotubes. Wat Res. 2011;45:4056–4068.
crossref

27. Lalhmunsiama , Tiwari D, Lee SMActivated carbon and manganese coated activated carbon precursor to dead biomass in the remediation of arsenic contaminated water. Environ Eng Res. 2012;17:S41–S48.
crossref pdf

28. Azizian SKinetic models of sorption: a theoretical analysis. J Colloid Interf Sci. 2004;276:47–52.
crossref

29. Ho YS, McKay GA comparison of chemisorption kinetic models applied to pollutant removal on various sorbents. Proc Saf Environ Protect. 1998;76:332–340.
crossref

30. Haerifar M, Azizian SAn exponential kinetic model for adsorption at solid/solution interface. Chem Eng J. 2013;215–216:65–71.
crossref

31. Tiwari D, Laldawngliana C, Lee SMImmobilized small sized manganese dioxide sand in the remediation of arsenic contaminated water. Environ Eng Res. 2014;19:107–113.
crossref pdf

Fig. 1
Effect of pH on the removal of E2 using different materials.
/upload/thumbnails/eer-21-2-203f1.gif
Fig. 2
Effect of initial E2 concentration on the removal of E2 using various hybrid materials.
/upload/thumbnails/eer-21-2-203f2.gif
Fig. 3
Effect of background electrolyte (NaCl) concentration on the removal of E2.
/upload/thumbnails/eer-21-2-203f3.gif
Fig. 4
Effect of contact time on the removal of E2 by various hybrid materials.
/upload/thumbnails/eer-21-2-203f4.gif
Fig. 5
Breakthrough curves for the removal of E2 using various hybrid materials.
/upload/thumbnails/eer-21-2-203f5.gif
Table 1
BET Pore Size, Specific Pore Volume and Specific Surface Area Values of the Clay and Hybrid Materials
Materials Pore Size (nm) Specific pore volume (cm3/g) BET Specific surface area (cm2/g)
BC 4.98 0.010 80.86
BCH 36.60 0.050 4.68
BCAH 27.45 0.075 9.55
LC 30.67 0.025 2.94
LCH 13.12 0.045 11.87
LCAH 8.04 0.010 4.55
Table 2
Kinetic Parameters Obtained for the Sorption of E2 by Hybrid Materials Using Various Kinetic Models
Systems Kinetic Models

PFO PSO FL-PSO



qe k1 s2 qe k2 s2 qe k α s2
BCH-E2 2.264 0.952 0.195 2.378 0.656 0.049 2.726 0.480 0.464 0.003
BCAH-E2 2.124 0.706 0.395 2.276 0.435 0.144 3.626 0.154 0.308 0.009
LCH-E2 2.208 0.841 0.304 2.340 0.546 0.098 3.040 0.298 0.368 0.009
LCAH-E2 1.914 0.633 0.346 2.065 0.412 0.126 3.358 0.147 0.324 0.011

[i] s2: Least Square Sum

Table 3
Thomas Constants (along with the least square sum) Estimated for the Removal of E2 by Various Hybrid Materials
Materials Thomas constants Least square sum (s2)

KT × 10−4 (L/min/mg) qo (mg/g)
BCH 1.86 75.984 9.2
BCAH 2.43 63.757 10.0
LCH 2.38 58.965 9.8
LCAH 2.47 49.746 16.0
Editorial Office
464 Cheongpa-ro, #726, Jung-gu, Seoul 04510, Republic of Korea
TEL : +82-2-383-9697   FAX : +82-2-383-9654   E-mail : eer@kosenv.or.kr

Copyright© Korean Society of Environmental Engineers. All rights reserved.        Developed in M2community
About |  Browse Articles |  Current Issue |  For Authors and Reviewers