Synthesis of metal–organic frameworks (MOFs) MIL-100(Fe) functionalized with thioglycolic acid and ethylenediamine for removal of eosin B dye from aqueous solution

The interaction of eosin B dye from aqueous solution with MIL-100(Fe) and functionalized MIL-100(Fe) metal–organic frameworks (MOFs) is reported in this study. MIL-100(Fe) was prepared and functionalized with thioglycolic acid (TH) and ethylenediammine (ED) separately by incorporating the thiol (–SH) and the amine (–NH2) group of the functionalizing agents into the open metal sites of the MIL-100(Fe) to obtain the acidic (TH-MIL-100) and basic (ED-MIL-100) forms of the MOF respectively. Characterization of the MOFs was done by melting point analysis, elemental analysis, spectroscopic techniques, scanning electron microscopy (SEM), and powdered X-ray diffraction (PXRD) analysis. The adsorption experiments were carried out at different conditions such as pH, adsorbent dosage, contact time, temperature, and initial concentration of the dye to estimate the optimum conditions and the maximum adsorption capacities. Adsorption capacities were observed to increase in the order of ED-MIL-100 < MIL-100 < TH-MIL-100, while the TH-MIL-100 was the most effective in the removal process due to acid–base interaction between the acidic thiol group (–SH) and the alkaline medium of eosin B dye solution. The Langmuir Isotherm was seen to fit well to adsorption data obtained for all three adsorbent materials studied, and adsorption processes followed the pseudo-second order kinetics. This study, therefore, indicates the suitability of functionalization of MIL-100(Fe) towards improving its adsorption capacity.


Introduction
Porous coordination polymers (Metal-organic frameworks (MOFs)) have been presented as emerging materials showing high degree of porosity and extensively studied due to unique characteristics which include structural flexibility and rigidity, high degree of pore volume, and their uniquely high specific surface area [1]. The internal surfaces of MOFs are also susceptible to tuning to achieve the desired characteristics enabling their preparation for specific purposes [1,2]. MOFs having rigid structures which possess pores that are well-defined having internal diameters of up to about 48 Å are able to present large free spaces which could accommodate guest molecules achieving MOFs that are applicable for the purpose of energy storage [3,4], adsorption and separation processes [5], in-pore assembly of nano particles [6,7], catalytic processes [8,9], and drug loading/delivery [10][11][12][13].
The functionalization of MOFs which is otherwise referred to as post synthetic modification enables the altering of MOFs surfaces by the introduction of functional groups on to the MOFs which changes the pore functionality of MOF, which results in selective interactions of the pores with guest molecules. The large number of available ligands with a variety of functionalities have enabled the achievement of MOFs having a variety of functional groups. However, synthesis processes using these ligands alone sometimes do not achieve the desired functionalities or MOF structure in these materials, hence, it becomes imperative in this case to develop alternative routes such as functionalization to achieve desired MOF properties by interacting the functional groups on the ligands with post synthetic functionalizing agents to generate MOFs having the desired characteristics [14,15]. The MIL-100(Fe) MOF is a crystalline three-dimensional material prepared from a combination of iron(III) salt and the tricarboxylate ligand (trimesic acid) and this material has been reported as one of the highly porous MOFs available. The two mesoporous cage sets (24 and 29 Å) are reportedly accessible through the microporous windows (ca.8.6 Å and ca.4.7-5.5 Å) of the material [16,17], and the non-toxic nature of the Fe 3+ ion which is inexpensive and environmentally friendly gives the MIL-100(Fe) its importance and desirability.
Synthetic dyes such as methyl red, malachite green, and eosin B, have been utilized as essential starting materials for colouring purposes in various industrial processes ranging from printing, textiles, cosmetics, and leather. However, the widespread use of this organic dyes has led to their increased discharge into environmental medias which poses significant danger to life and the environment due to their toxic nature at elevated concentrations. Technologies and procedures have been designed with the aim of removing these toxic substances from the environment. Utilized procedures for removing dyes from the environment include biological treatment, membrane filtration method, and adsorption. The adsorption procedure is reported to be the most widespread used technique for environmental remediation of dyes due to its effectiveness and good colour removal potential. Materials such as zeolites and activated carbon have been used as adsorbents for the removal process, however, their use for dye removal have been restricted due to small pore diameter which limits efficiency of dye adsorption [18,19]. Hamedi et al. [18,19] prepared new MOF composite of MIL-101(Fe)@ PDopa@Fe 3 O 4 and MIL-100(Fe)@Fe 3 O 4 @AC nanocomposite for the removal of methyl red (MR), malachite green (MG), and rhodamine B (RhB) dye pollutants from the environment. The MIL-101(Fe)@PDopa@Fe 3 O 4 adsorption capacity was obtained to be 1250 mg/g at 298 K for MR and 833 mg/g at 318 K for MG and observed to be of better efficiency than other adsorbents. The ability of the prepared MIL-100(Fe)@Fe 3 O 4 @AC to adsorb RhB dye was observed to be 769.23 mg/g, and also found to be higher than other adsorbents which has been utilized for the same process.
Interestingly, an effective assembly strategy via the premodification of organic ligands and/or post-modification of prepared MOFs is important for the construction of novel MOFs which have found application in several processes [20] including dye encapsulation [21]. Hong et al. [22] prepared a series of mesoporous Zn-MOFs by coordinating zinc(II) ion with of 9-fluorenone-2,7-dicarboxylic acid (H 2 FDCA), dibenzo[b,d]thiophene-3,7-dicarboxylic acid 5,5-dioxide (H 2 DTDAO), and fluorene-2,7-dicarboxylic acid (H 2 FDC) which were utilized as adsorbents for the removal of methylene blue (MB) from aqueous media, and reported that the Zn-MOFs were observed to be excellent adsorbents for the removal of MB. Masoomi et al. [23] investigated the photocatalytic activity of three Zn(II) MOFs formulated as TMU-4, TMU-5, and TMU-6 which were prepared by a mechanochemical technique, in the decolorization of the congo red dye. It was observed that the photocatalysts were also able to mineralize and degrade the dye even in the absence of oxidants such as H 2 O 2 . Abdollahi et al. [24] also prepared a new Zn-MOF, and formulated as TNU-39, by the ultrasonic irradiation and solvothermal techniques, and investigated the ability of this MOF in the removal of congo red (CR) and sudan red (SR) dyes. It was observed that removal efficiency for SR was higher than that of CR and attributed this to the smaller size of the SR dye molecules.
The eosin B dye is reported to be a very reactive organic dye with hazardous effects in the environment [25]. The combination of this dye with other synthetic dyes for domestic and industrial purposes has seen a considerable increase over the last decades. These dyes are employed in the manufacture of materials such as clothing, paper, leather, amongst others to achieve colourful designs and to make these items attractive. Wastes generated from the use of these dyes are usually discarded indiscriminately thereby polluting the environment in the process [1][2][3][4]. These effluents usually are able to block sunlight and oxygen from penetrating into water bodies depriving aquatic forms of life the essential ingredients of their survival. Also, these dyes can undergo degradation into compounds which have the potential of being carcinogenic and end up in the food chain [26,27] necessitating the need to urgently remove these chemicals from wastewater before discharge [16].
This work focuses on functionalization of MIL-100(Fe) by incorporating the thio-and amine-functional groups unto the prepared MIL-100(Fe) using thioglycolic acid and ethylenediamine thereby achieving new functionalized MIL-100(Fe) materials as a platform for environmental remediation of dyes. The ability of these functionalized MIL-100(Fe) materials to adsorb and remove the eosin B dye from the environment is studied. To the best of our knowledge, there is limited information on functionalization of MIL-100(Fe) and particularly with thioglycolic acid and ethylenediamine for use in the removal of eosin B dye. Thus, we report the preparation and functionalization with thioglycolic acid and ethylendiamine of MIL-100(Fe) and their use as adsorbents for the removal of eosin B dye from aqueous media.

Synthesis of MIL-100(Fe) adsorbents
The MIL-100 was synthesized based on method previously described [17,28]. Iron(III) nitrate nonahydrate (10 mmol, 4.04 g) was weighed and dissolved in 50 ml of deionized water, 9 mmol (1.89 g) of trimesic acid was also weighed and dissolved separately in 50 ml of ethanol. The solutions were mixed together and refluxed for 12 h at 95 °C. Precipitate formed was filtered, washed with deionized water/ ethanol (50:50), and dried at room temperature. Thereafter, it was activated in a vacuum oven at 150 °C for 10 h, and stored in a desiccator.
Functionalization of the synthesized MIL-100 was carried out by modifications to a previously reported procedure [29]. For the TH-MIL-100, 0.3 g of the dehydrate MIL-100(Fe) was weighed into 10 ml of anhydrous toluene and 1 ml of thioglycolic acid (TH) was added to the suspension. This mixture was continuously refluxed at 120 °C for 12 h to obtain an optimized grafting, and the resulting solid was washed severally with deionized water/ethanol (50:50), dried at room temperature, and stored in a desiccator. The same procedure described above was followed for the preparation of the ED-MIL-100, however, thioglycolic acid was replaced with ethylenediamine (ED). The equation of reactions is presented in Schemes 1, 2, 3, 4 below.

Characterization of the MOFs
The melting points of the MOFs were determined using a Gallen-Kamp melting point apparatus. Elemental analysis was performed on a Perkin-Elmer CHN Analyzer 2400 series II. UV-Visible measurements were performed on a SHIMADZU UV-1650 UV-VIS spectrophotometer. Fourier transform infrared (FT-IR) analysis was performed using a SHIMADZU scientific model FTIR 8400 s spectrophotometer. Brunauer-Emmett-Teller surface area analysis was carried out using NOVA 4200e BET instrument.

Adsorption studies
Adsorption studies were carried out following a procedure previously reported by [30][31][32][33]. Adsorption of eosin B dye onto the adsorbents (MIL-100(Fe), TH-MIL-100, and ED-MIL-100) was studied using eosin B stock solution of 1000 mg/L. This was prepared by dissolving 0.1 g of the eosin B dye in 1000 ml of deionized water. Lower concentrations of the dye (5-30 mg/L) were prepared from the stock solution by serial dilution with deionized water, and the concentration of eosin B determined from absorbance measurement at λ max of 530 nm using a SHIMADZU UV-1650pc Ultraviolet-Visible (UV-Vis) spectrophotometer. The calibration curve ( Fig. 1) was plotted using absorbance values obtained from the eosin B working standards of 5-30 mg/L. Before adsorption study, the MIL-100 was dried for 12 h at 150 °C. The activated MIL-100(Fe) and functionalized MIL-100 adsorbents (0.02 g of each) were then added to the prepared solutions separately and the mixtures were shaken for 2 h. Absorbance readings were taken using the UV-Visible spectrophotometer (SHIMADZU UV-1650pc Ultraviolet-Visible (UV-Vis) spectrophotometer) at a λ max of 530 nm. The effect of concentration, temperature, time, pH, and adsorbent dosage on the adsorption process was also determined and absorbance before and after the adsorption process was taken to determine the quantity (q e ) of eosin B (mg/g) dye adsorbed at equilibrium using the formula: where C o and C e (mg/L) are the initial and final concentrations of the adsorbates respectively, v is the volume of the solution used (ml) and m is the mass (g) of the adsorbents . The effect of time was studied at time interval of 30-180 min, while the effect of temperature was studied at temperature range of 30-70 °C. The effect of pH was studied by varying the pH between 2 and 13 using 0.1 M HCl or 0.1 M NaOH, while the effect of adsorbent dosage was studied using 0.01-0.05 g of the adsorbents, and the effect of concentration was studied using 5-30 mg/L of the adsorbate.

Characterization of MIL-100 adsorbents
Physico-chemical parameters and elemental analysis of the MIL-100, TH-MIL-100, and ED-MIL-100 prepared are presented in Table 1. The melting point of MIL-100 prepared was observed to increase after functionalization.

Spectroscopic analysis
The Fourier-transform infrared (FT-IR) spectrum of the synthesized MIL-100 in this study was compared with previously reported spectrum of the MOF [27]. The pattern shows bands at 3430, 1720, 1382 and 1450 cm −1 correlated with the 3500, 1720, 1350, and 1480 cm −1 of the previous report [27]. A 0.195 g yield was obtained for the TH-MIL-100 representing a 65% yield, and the FT-IR spectrum of the functionalized MIL-100 with thioglycolic was found to be similar to that of the synthesized MIL-100, with  additional bands owing to coordination between the MIL-100 and the functionalizing agent. The presence of these new bands was further confirmed by comparing them with the spectrum of a thiol functionalized MOF reported by [30]. The synthesized TH-MIL-100 showed additional bands at 3000, 2659, and 621 cm −1 correlating with the thiol functionalized MOF reported by [30], which are 2900, 2581 and 686 cm −1 assigned to ʋ(C-H), ʋ(S-H), and ʋ(C-S) vibrations respectively. The yield obtained for the ED-MIL-100 was calculated to be 0.225 g, representing a 75% yield. The FT-IR spectrum of the functionalized ED-MIL-100 is also similar to the synthesized MIL-100 with additional bands owing to coordination between the MOF and the functionalizing agent (ethylenediammine). The presence of these new bands was established by comparing them with the spectrum of an ethylenediammine functionalized MOF reported [27]. The synthesized ED-MIL-100 showed bands at 1560, 1030, and 958 cm −1 which correlated well with the bands in ethylenediammine functionalized MOF previously reported [27]. The absorption bands observed at 1598, 1040 and 986 cm −1 were assigned to the ʋ(N-H), ʋ(C-N), and ʋ(N-H 2 ) stretching vibrations respectively [27]. UV-vis spectrum (  [33] in the proposed octahedral geometry of a complex. Table 2 and Fig. 2a-c presents the FT-IR absorption bands of the prepared MOFs.

SEM analysis
The surface morphologies and chemical compositions of the virgin and the functionalized MIL-100 samples were observed by scanning electron microscopy (SEM) and presented in Fig. 3a-c. The image of the MIL-100 before functionalization showed a smooth crystalline surface. However, upon functionalization, morphological transformation occurred and the surfaces became rough suggesting that there was partial distortion of the framework during the functionalization process of the MOF [34].

Powder X-ray diffraction analysis results
The PXRD patterns of the MIL-100, TH-MIL-100, and ED-MIL-100 is presented in Fig. 4. The pattern of MIL-100 shows characteristic peaks at 2Ɵ value of 26.58°, 27.48°, and 27.98° which is comparable with values reported [17,28]. Peak observed at 20.94° and 24.1 in the MIL-100 material was seen at 20.24°and at 24.86° in the TH-MIL-100. The PXRD pattern of the prepared materials are presented in Fig. 4.

Effect of concentration
The result of the effect of concentration of the eosin B dye on the adsorption process using different adsorbents is shown in Fig. 6. The amount of the eosin B dye adsorbed on the adsorbents was observed to increase as the concentration of the dye increased reaching a maximum at 25 mg/L for MIL-100 and TH-MIL-100, and 20 mg/L for ED-MIL-100. The adsorption sites on the adsorbents were observed to become saturated as the concentration of eosin B dye increased, resulting in subsequent desorption of the dye as the process continued. Increased competition between the molecule of the eosin B dye for adsorption sites on the adsorbent resulted in an initial increase in the adsorption process followed by a subsequent slowing down of the process [16]. This phenomenon is attributed to the fact that at a low concentration of the dye, solute to adsorbent vacant sites ratio is high, which results in an increase in the removal of the dye [16]. The result also showed that the adsorption capacities of the three adsorbents increased in the sequence of TH-MIL-100 > MIL-100 > ED-MIL-100.

Effect of time
The effect of time on the adsorption of eosin B dye onto the adsorbents shown in Fig. 7 indicates that the adsorption efficiency increased gradually with increase in contact time and reached a maximum value after 60 min for MIL-100, TH-MIL-100, and ED-MIL-100 and remained constant thereafter. The experiment was carried out at pH 8.0 using 25 mg/L dye concentration for MIL-100 and TH-MIL-100, and 20 mg/L dye concentration for ED-MIL-100; 0.02 g adsorbent dosage for 30-180 min duration in order to determine the equilibrium time for the adsorption process. The increase in adsorption at the commencement of the process is attributed to the availability of vacant adsorption sites on the adsorbents, which became occupied with time [35].

Effect of temperature
The effect of temperature increase on the adsorption process of eosin B dye on the adsorbents was studied using the equilibrium solution concentrations of dye for each of the adsorbents (i.e. 25 mg/L for MIL-100 and TH-MIL-100, and 20 mg/L for ED-MIL-100), and 0.02 g of the adsorbent at a pH value of 2.0 for MIL-100 and ED-MIL-100, and 8.0 for the TH-MIL-100, by varying the temperature between 30 and 70 °C, for a period of 60 min for each experiment. The result of the study shown in Fig. 9 indicated that increase in temperature had very minimal effect on the adsorption process.

Effect of adsorbent dosage
The effect of adsorbent dosage on the adsorption of eosin B dye onto the adsorbents was studied using the equilibrium concentration of dye solution of 25 mg/L for MIL-100 and TH-MIL-100, and 20 mg/L for ED-MIL-100, while the amount of adsorbent used was varied from 0.01 to 0.05 g at a pH of 2.0 for MIL-100 and ED-MIL-100, and 8.0 for the TH-MIL-100 for a period of 60 min for each experiment (Fig. 10). The removal process was observed to increase as the adsorbent quantities increased due to an increase in adsorption sites amount of the adsorbents was increased which was accompanied by an increase in adsorbents and consequently, available adsorption sites [37]. The adsorption of the eosin B dye on the MIL-100 and TH-MIL-100 reached a maximum with an adsorbent dose of 0.03 g for the process involving MIL-100 and TH-MIL-100, and 0.02 g adsorbent for the process involving ED-MIL-100.

Comparison of UV-Vis spectra measurements before and after adsorption
The UV-Vis spectra of the adsorbents were obtained before and after the adsorption process, compared and the result presented in Table 3.
The results showed shifts in absorption band wavelengths of the three adsorbents after adsorption from 359 nm cm − 1, 362 nm and 464 nm to 393 nm, 410 nm and 553 nm respectively for MIL-100; 350 nm, 360 nm, and 488 nm to 354 nm, 415 nm and 554 nm respectively for TH-MIL-100; and 348 nm and 496 nm to 350 nm and 544 nm respectively for ED-MIL-100. The absorption band wavelengths shifted to higher value towards the visible region of the spectra, this is probably due to adsorption of the dye by the MOFs [38].

Equilibrium adsorption isotherm studies
Information about adsorption mechanism can be obtained from the equilibrium adsorption isotherms using isotherms models such as Langmuir, Freundlich, Tempkin, and Dubinin-Radushkevich [D-R]. Figures 11,12,13,14 shows the plot of the various isotherms for the adsorption process and the parameters of the isotherm equations summarized in Table 4.
The linear form of the Langmuir isotherm model gave the values of K a [the Langmuir adsorption constant (L/mg)] and Q m [theoretical maximum adsorption capacity (mg/g)] obtained from the intercept and slope of the plot of C e / Q e versus C e , respectively. Adsorption onto an adsorbent is assumed to be a monolayer adsorption with no interaction between the adsorbate molecules [35,39]. Correlation  where K a (L/mg) is the Langmuir constant and C o (mg/L) is the initial concentration. The adsorption process can be determined as favorable when the R L value lies between 0 and 1 [36]. It was found that for the three MIL-100 adsorbents the R L values are lower than 1, suggesting the favorable adsorption and the fitness of Langmuir model to the experimental data. The Freundlich isotherm model parameters such as K f [(mg g −1 )/(mg L −1 )] and 1/n were obtained from the intercept and slope of the linear plot of ln q e versus ln C e , respectively. K f = Freundlich constant which indicates the extent of adsorption; 1/n = heterogeneity factor (adsorption effectiveness).
(2)  The 1/n value of 0.15-0.52 obtained indicates the favorable adsorption and high tendency of eosin B dye for adsorption onto the unfunctionalized and functionalized MIL-100(Fe) adsorbents, while lower R 2 values (0.2293-0.8334) for the adsorbents indicates that the Freundlich model less fits the experimental data [35,37].
The heat of the adsorption and the adsorbent-adsorbate interaction was evaluated using Tempkin isotherm model. In this model, B l is the Tempkin constant related to heat of the adsorption (J/mol), T is the absolute temperature (K), R is the universal gas constant (8.314 J/mol/K) and K T is the equilibrium binding constant (L/mg). The values of the Tempkin constants (1.10-2.26) and the correlation coefficient (0.1784-0.7714) are lower than the Freundlich and Langmuir values, indicating that the Tempkin isotherm is a lesser fit for the experimental data than both Langmuir and Freundlich isotherms. The Dubinin Radushkevich model was applied to estimate the porosity apparent free energy and the characteristic of adsorption. In this model, K (mol 2 /(kJ 2 )) is a constant related to the adsorption energy, Q s (mg/g) is the theoretical saturation capacity, and e is the Polanyi potential. The slope of the plot of ln q e versus ε 2 gives K and the intercept gives the Q s value. The D-R equation was seen to represent a poor fit for the experimental data for MIL-100 and ED-MIL-100 but suitable for TH-MIL-100.
The correlation coefficient of the Langmuir isotherm was observed to be higher than that of the other isotherms, which suggests that the adsorption process of eosin B dye onto the three adsorbents can better be (5) q e = B I lnK T + B I lnC e (6) lnq e = lnQ s − B 2 described with the Langmuir model and the adsorption is a monolayer adsorption in addition to Dubinin Radushkevich model which fits in for TH-MIL-100 [40][41][42].

Adsorption kinetic
The pseudo-first-and second-order kinetics, Elovich and intraparticle diffusion models were used to study the rate and mechanism of adsorption process, and the results are presented in Table 5 with the equations for the models. The pseudo-first-order model (Lagergren model) was obtained by a plot of the values of log (q e -q t ) versus time, and values of k 1 and q e were determined from the slope and intercept of the graph respectively (Fig. 15). The difference between the intercept and the experimental q e value indicates that this model does not explain the experimental data and rate of adsorption does not follow this equation [42,43]. The validity of the model was further checked by the correlation coefficient (R 2 ). The low R 2 values again showed that the pseudo-first-order model does not fit well with the experimental data. The plot of t/q t versus t for the pseudo-second-order kinetic model gave a straight line with a high correlation coefficient (R 2 ) (Fig. 16). The k 2 and equilibrium adsorption capacity (q e ) were calculated from the intercept and slope of this line, respectively. The high values of R 2 (0.99) and closeness of experimental and theoretical adsorption capacity (q e ) value show the applicability of the pseudosecond-order model to explain and interpret the experimental data [42,43]. The intra-particle diffusion model is shown in Fig. 17.
The intraparticle diffusion model based on diffusive mass transfer that adsorption rate can be expressed in terms of the square root of time (t) [44][45][46][47][48] was also applied. The values of K diff [the intraparticle diffusion rate constant (mg/g/min 1/2 )] and C (thickness of the boundary layer) were calculated from the slope and intercept of the plot of q t versus t 1/2 respectively (Fig. 17) and the results are presented in Table 5.
The Elovich equation is another rate equation based on the adsorption capacity in linear form, which has been successfully applied for the adsorption of solutes from a liquid solution [44,45]. The plot of q t versus ln (t) gives a linear relationship (Fig. 18) with a slope of (1/b) and an intercept of (1/b)ln(ab). The Elovich constants obtained from the slope and the intercept of the straight line are reported in Table 5. The correlation coefficients (R 2 ) were observed to be low showing that this model is unsuitable for complete evaluation of the adsorption process [44].
From the results in Table 5, it is obvious that the adsorption of the dye followed the pseudo-second-order kinetics. The theoretical values obtained were close to experimental values with correlation coefficients > 0.99, which fitted better than the other kinetic models for the entire adsorption process. Therefore, it can be concluded that pseudo-second-order equation is better in describing the adsorption kinetics of eosin B on MIL-100 adsorbents and therefore the rate of reaction appeared to be controlled by the chemical interaction [47][48][49][50][51][52].

Adsorption Mechanism
The surface area of the three adsorbents are in order of MIL-100 > > ED-MIL-100 > TH-MIL-100 but the adsorption capacities were in order of TH-MIL-100 > MIL-100 > ED-MIL-100. Contrary to the rule, the materials with large surface are expected to have excellent adsorption, but it is interesting to note that TH-MIL-100 with lowest surface area has highest adsorption, this indicates that porosity/ surface area is not the only factor determines adsorption capacity. It can be observed that functionalization of MIL-100 with thioglycolic acid and ethylenediamine generates acidic SO 3 H and basic NH 2 . The only possible   mechanism that can explain the highest adsorption capacity of TH-MIL-100 for Eosin-B is therefore electrostatic interaction between the positive charged surface of TH-MIL-100 via incorporation of thioglycolic acid and anionic dye(negatively charged). The acidic TH-MIL-100 may result to acid-base interaction during the adsorption of the eosin-B dye because of the acidity of the adsorbent and the COO − of the eosin-B.

Comparison of adsorption capacity
The adsorption of capacity of the materials prepared were compared with that obtained by other researchers for the removal of eosin B dye from the environment and presented in Table 6. It was observed that the prepared materials compared favourably well with other materials prepared in similar researches.

Reusability experiments
The reusability of the MIL-100(Fe) and the functionalized MIL-100(Fe) materials for the removal of eosin B dye from aqueous medium was investigated for each compound. The optimum conditions of 25 mg/L for MIL-100 and TH-MIL-100; and 20 mg/L for ED-MIL-100, equilibrium time of 60 min, and optimum pH of 13 for TH-MIL-100 and MIL-100; and at pH of 2 for ED-MIL-100 materials, and adsorbent doses of 0.03 g for MIL-100 and TH-MIL-100; and 0.02 g for ED-MIL-100 were employed for the reusability experiments. The percentage removal was calculated using the calibration curve and absorbance value obtained. The results indicated that the materials can be reused as adsorbents for the removal of eosin B dye from aqueous medium for more than three runs with decreasing value of removal efficiency for each run (Fig. 19).

Conclusion
The low-cost metal-organic frameworks (MIL-100(Fe) were prepared using simple synthesis route. The synthesized MOFs were used as adsorbents for the removal of eosin B dye from aqueous solution. The results showed that the synthesized MOFs have high adsorption capacity for eosin B dye. The adsorption process was fast and reached equilibrium within 90 min. The TH-MIL-100 was found to be the most effective in the removal of eosin B, due to the presence of the thio-group on the TH-MIL-100 material as observed in the results of the BET analysis carried out. The acid-base interaction between the adsorbent and the adsorbate due to the presence of thioglycolic acid molecules which made the MOF acidic is also suggested as improving the removal efficiency. Langmuir isotherm gave a better fit to adsorption isotherms. The kinetic study of eosin B onto MIL-100 s adsorbents indicated that the adsorption kinetics followed the pseudo-second-order rate. Optimum conditions obtained for maximum adsorption of eosin B dye on the adsorbents were observed to be at dye concentrations of 25 mg/L for MIL-100 and TH-MIL-100, and 20 mg/L for ED-MIL-100. The equilibrium time for maximum adsorption was observed to be 60 min, while optimum pH was observed to be 13 for TH-MIL-100 and MIL-100, and at pH of 2 for ED-MIL-100. Increase in temperature was observed to have no appreciable effect on the adsorption process, while the maximum adsorption capacity was observed for adsorbent doses of 0.03 g for MIL-100 and TH-MIL-100, and at 0.02 g for ED-MIL-100. The results of this study suggest that low cost MOFs obtained using simple approach like ours could be utilized as effective adsorbents for the adsorption of dyes from wastewater.  [54] 16.28 Kant [55] 48.8 Kanwal et al. [56] 7.96

Compliance with ethical standards
Conflict of interest The authors declare that there is no conflict of interests concerning the publication of this article.
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