BARIUM CHLORIDE MODIFICATION OF DIATOMITE FOR REMOVAL OF METHYLENE BLUE AND LEAD ION AQUEOUS SOLUTION

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ISSN: 974-1496 e-issn: 976-83 CODEN: RJCABP http://www.rasayanjournal.com http://www.rasayanjournal.co.in BARIUM CHLORIDE MODIFICATION OF DIATOMITE FOR FROM AQUEOUS SOLUTION Le Van Tan * and Le Thiet Hung Department of Chemical Engineering, Industrial University of Ho Chi Minh City-7, Vietnam * E-mail: levantan@iuh.edu.vn ABSTRACT In this research, the surface of natural diatomite was modified with Barium chloride by hydrothermal method for removal of methylene blue and lead ions. The characterization of natural and modified diatomite was investigated by SEM, FT-IR and XRD. The Brunauer-Emmett-Teller (BET) surface area exhibited that the similar surface areas were obtained between the clean diatomite and modified diatomite. In this study, modified diatomite was attempted to enhance the adsorptive capabilities of diatomite for methylene blue and lead ions. The effect of some operational parameters such as initial concentration and ph on the adsorptive capacity of the diatomite was tested. The sorption rate was affected significantly by the initial concentration of the solution, sorbent amount and ph value of the solution. Batch experiments were conducted to investigate the adsorption effect under different initial concentration (ranging from 5 to mg/l), solution ph (4, 6, 8 and 1), and contact time (.5 to 12h). Keywords: diatomite, methylene blue, heavy metal, wastewater RASĀYAN. All rights reserved INTRODUCTION Dyes are widely used in broad industrial sectors such as textile manufacturing, leather tanning, cosmetics, paper, food processing, and pharmaceutical industries. There are many classes of dyes such as azo, anthraquinone, reactive, acidic, basic, neutral, disperse and direct dyes. It is estimated that 5 5 % of unfixed dyes are lost in the effluent during the dyeing process 1. The growth in the textile dyeing and dyestuff manufacturing industries has resulted in a proportional increase in the volume and complexity of the wastewater discharged to the environment. Chemical pollution caused by these processes has become a concern for many countries which urgently requires environmental measures. These compounds color the water and make penetration of sunlight to the lower layers impossible and hence affecting aquatic life. Many of these are toxic, carcinogenic, mutagenic, or even stable to biological degradation 2. A wide range of methods have been developed for the removal of textile dyes from the wastewaters such as biological methods, membrane filtration, coagulation flocculation, electrocoagulation and adsorption 3,4. Activated carbon is a frequently used method to removal organic pollutants from wastewater but is an expensive material and its use for pollution control applications cannot be justified. The research has been directed towards methods of treatment using natural materials, locally available and effective adsorbents, such as natural diatomite. Diatomite is a material of sedimentary origin consisting mainly of an accumulation of skeletons formed as a protective covering by diatoms. The skeletons are essentially amorphous hydrated or opaline silica but occasionally are partly composed of alumina. Diatomite usually contains other sediments such as clay and fine sand but its deposits sometimes consists of diatom shells only 5. However, the raw diatomite frequently contains an important rate of impurities that can restrain its efficiency in many applications 6. In this present research, modification of diatomite surface by barium chloride was reported and its use in adsorption of heavy metal ions and textile dyes in wastewater. 478

EXPERIMENTAL Adsorbent Preparation The diatomite sample was obtained from Hoa Loc, Phu Yen (Viet Nam) and the chemical composition of diatomite obtained by X-ray florescence (XRF) is 82.4% SiO 2, 8.95% Al 2O 3, 6.49% Fe 2O 3,.483% MgO,.175% K 2O and.13% CaO. Firstly, g of diatomite ( mesh) were immersed in ml of BaCl 2 solution with various concentrations (15- g/l), a certain amount of.5 mol/l H 2SO 4 was immediately added into the mixture and then shook at room temperature for 3 h under mechanical stirrer. Then, the mixture was exposed to air for 12 h and discard the supernatant and afterwards dried in an oven at 15, 3, and 5 o C for 24 h. Finally, the samples were grinded to mesh and stored in the dry box for further study. The prepared samples were named as DA3T15, DA3T3, DA3T, DA3T5; DAT15 DAT3, DAT, DAT5; DAT15, DAT3, DAT, DAT5. Characterizations The mineral phase of diatomite was characterized by X-ray diffraction (XRD) (Rigaku, Japan). The surface of diatomite and modified-diatomite was observed by using a scanning electron microscope (SEM, JEM-). X-ray fluorescence spectrometer (XRF) provided us the element contents. Adsorption Experiments Synthetic industrial wastewater was used in the adsorption studies. The solution was prepared by dissolving methylene blue (MB) in deionized water. Lead (II) stock solution ( mg/l) was prepared by dissolving the 1.598 g Pb(NO 3) 2 salts in ml deinoized distilled water. All the solutions for lead removal experiments and analysis were prepared by an appropriate dilution of the stock solution. Adsorption of modified diatomite was performed in a set of Erlenmeyer flasks (25 ml) contained 25 ppm MB solutions ( ml). The difference types of prepared diatomite (.5g) was added to MB solutions, and the resulting mixtures were then kept at room temperature. The aqueous samples were taken at determined intervals, and the concentrations of dye were measured at 665 nm, using UV vis spectrophotometer. The amount of adsorption at time t, q t (mg/g), is calculated by q t = (C C t)*v/w where C and C t (mg/l) are the liquid-phase concentrations of MB at initial and any time t, respectively; V is the volume of the solution (L) and W is mass of absorbent (g)..5 g of diatomite and ml of Pb(NO 3) 2 solution 5 ppm were added in 15 ml conical flask and then were placed in a shaker with a speed of rpm. The concentrations of Pb ions remaining in the supernatant were measured using standard methods recommended for examination of water and wastewater 7. RESULTS AND DISCUSSION Preparation and characterization of diatomite The structure of modified diatomites were characterized by FT-IR, XRD, and SEM. In Figure 1, the general range 37 34 cm 1 may be assigned to asymmetrical and symmetrical O-H stretching vibration modes for water of hydration and the peak at 1632 cm 1 belonged to O-H bending vibration modes. The presence of SiO 2 is verified by adsorption bands at 197 cm 1 of asymmetric Si-O-Si stretching vibrations, and Si-O-Si bending vibrations at 468 cm 1. In brief, XRD patterns of 12.,.85, 26365, 34.95, 5.15, 5.9, 62. o. The X-ray diffraction spectra displayed that silica was the major component. The cristobalite, quartz and feldspar noteworthy were revealed in the range of 25< 2θ <33 in the X-ray diffraction spectra, respectively (Fig.-2).The scanning electron microscope shows that the main pattern of the diatomite was discoid and the surface was porous structure. However, modified diatomite was relatively uneven and a number of pores were filled, it illustrates that the expected barium sulphate formed in the interspaces. Additionally, there was several BaSO 4 crystals separated out on diatomite surface and its pores. Batch Adsorption Studies In this study, the various amounts of BaCl 2 from 15 to g/l were conducted for the removal efficiency of MB on modified diatomite. The results were shown in Figure 4. The removal efficiencies were 479

increased with increasing the concentration of BaCl 2 from to about g/l and decreased with rising of BaCl 2 concentration to g/l. This may be explained that deposition of BaSO 4, which was obtained from the reaction of BaCl 2 and H 2SO 4, improved pore structure of the diatomite, the impurities on the diatomite surface were eliminated by rubbing of BaSO 4, and the inner-channels in the diatomite were under-propped by BaSO 4, this was favorable for adsorption of MB onto the diatomite. Fig.-1: FTIR spectra of modified diatomite (DA15T15) and natural diatomite (MDA) Fig.-2: XRD patterns of modified diatomite (DA) and natural diatomite (MDA) 4

The removal efficacy was increased from 78 to 95% for natural diatomite and modified diatomite with g/l, respectively and decreased to 86% when the concentration of BaCl2 was increased to g/l. The results showed that the best concentration of the BaCl2 solution for the diatomite chemical modification was 15 g/l. At optimized concentration of the BaCl2 solution for the diatomite chemical modification, the several dried temperatures are conducted. As results, when calcination temperature was increased from 15 to 5 oc, the adsorption efficiency was decreased. The maximum adsorption efficiency was at 15 o C (Figure-5). (a) (b) Fig.-3: SEM images of (a) diatomite; (b) modified diatomite Effect of Initial Dye Concentration The effect of initial concentration on the MB removal was shown in Figure 6. As results, it is remarkable that an increase in the initial concentration (5 ppm) of MB led to a decrease in the removal efficiency of diatomite at various contact times. This can be attributed to the mass transfer effects and the driving force of the concentration gradient being directly proportional to the initial concentrations. The plateau values indicated that the adsorption equilibrium was gradually attained. The maximum removal efficiencies were obtained within 2 min for all concentrations. The removal efficiencies were 98, 91 and 76 for concentrations of 5, and ppm, respectively. The removal efficiency dropped to 64% for natural diatomite at concentration of ppm. Particularly, the UV-Vis absorption spectrum of MB at t = min was highest due to no adsorption between diatomite with MB molecules. Otherwise, the lowest absorption spectrum of MB was more than 4 min (Figure-7). The dependence of MB dye adsorption on diatomite dosage was studied by varying the adsorbent amount from.5 to.2 g while keeping the volume, 5 ml, of the dye solution constant ( ppm). The results indicate that the percentage adsorption increases with increasing amount of adsorbent. The increase in the percentage adsorption with increasing amount of the sorbent is due to the greater availability of the adsorption sites at higher concentrations of the adsorbent (Figure-8). Effect of various textile dyes A study of adsorption capacity of various textile dyes on the modified diatomite under the best condition in aqueous solution was conducted; the results are shown in Figure-9. As can be seen, different textile dyes showed various removal efficiencies. The results show that methyl blue, methyl red and cationic blue adsorption on diatomite is very fast compared to that of reactive red and reactive yellow. 481

1 Adsorption effciecny %) 15 3 Concentration of BaCl 2 (g/l) Fig.-4: The influence of the BaCl 2 solution concentration on the removal efficiency. Fig.-5: The change in absorption spectra of MB for adsorption onto diatomite modification with BaCl 2 15g/L dried at the various calcination temperatures. Adsorption effciecny (%) 1 5ppm ppm ppm DA with ppm MB 2 4 6 8 1 12 14 Time (min) Fig.-6: Effect of initial concentration and contact time on equilibrium adsorption. 482

Fig.-7: The change in absorption spectra of MB for concentration of ppm, modification of BaCl 2 15g/L at 15 o C. 1 Adsorption effciecny %) DA15T15 DA.5.1.15.2 Amount of adsorbents (g) Fig.-8: Adsorption efficiency of MB onto different amount of diatomite (initial concentration of MB: ppm; solution volume: ml). Removal of Pb 2+ Figure-1 showed that the curve of removal efficiency of Pb 2+ on modified diatomite with various concentration of BaCl 2. The efficiency was increased with increasing of the BaCl 2 solution concentration. At low concentration, the deposition of BaSO 4, which was obtained from the reaction of BaCl 2 and H 2SO 4 led to improve pore structure of the diatomite. Additionally, the impurities on the diatomite surface were eliminated by rubbing of BaSO 4, and the inner-channels in the diatomite were under-propped by BaSO 4, this was favorable for adsorption of Pb 2+ onto the diatomite. At high concentration, the deposition of 483

BaSO 4 restrained adsorption of Pb 2+ on the diatomite due to its block; this led to decrease of the diatomite adsorption capacity against Pb 2+. 1 Adsorption effciecny %) Metyl blue Metyl red Reactive red Reactive yellow Cationic blue Fig.-9: Effect of ph of dye solution on removal efficiency. Adsorption effciecny %) 9 7 5 3 1 15 3 Fig.-1: The effect of BaCl 2 concentration on the removal efficiency of Pb 2+ CONCLUSION In this present study, the modification of diatomite by BaCl 2 has successfully prepared and characterized. This study shows that diatomite is potential sorbent for removal of textile dyes from water. Diatomite is a locally available, low-cost adsorbent in Viet Nam. Comparing with the natural diatomite, the adsorption 484

efficiency for textile dyes on modified diatomite was higher than that of natural diatomite. Additionally, the adsorption efficiency for the lead ions increased from 61% to 75%, indicating that Ba-diatomite was an effective absorbent for removing lead ions from wastewater. REFERENCES 1. A.Maljaei, M. Arami and N.M. Mahmoodi, Desalination,249, 174(9). 2. E.Ozturk, M.Karaboyacı, U.Yetis, N.O. Yigit and M. Kitis, J. of Cleaner Production, 88, 116(15). 3. O. Sahu, B. Mazumdar and P. Chaudhari, Environmental Science and Pollution Research, 21, 2397 (14). 4. M.T. Yagub, T.K. Sen, S. Afroze and H.M. Ang, Advances in Colloid and Interface Science 9, 172 (14). 5. H.Abdollahi, Anal. Chim. Acta, 442, 327 (1). 6. E. Erdem, G. Çölgeçen and R. Donat, J. of Colloid and Interface Science 282,314 (5). 7. Standard methods for the examination of waste water th edition. American Public Health Association, American Water Works Association: (1999). [RJC-14/16] 485