Cationic dye (MB) removal using polymer inclusion membrane (PIMs)

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1 Available online at Procedia Engineering 33 (2012 ) ISWEE 11 Cationic dye (MB) removal using polymer inclusion membrane (PIMs) Aitali Salima, Kebiche-Senhadji Ounissa*, Mansouri Lynda and Benamor Mohamed Laboratoire des matériaux organique, université de Béjaia, DZ-06000, Béjaia Algeria. Abstract Studies were carried out to remove a basic dye (Methylene Blue; MB) from their aqueous solutions using polymer inclusion membranes (PIMs) consisting of Cellulose Triacetate (CTA) as the base polymer, 2-Nitrophenyl octyl ether (2-NPOE) as the plasticizer and Di-(- Ethyl hexyl) phosphoric acid (D2EHPA) as the carrier. The manufactured membranes have been characterized by Scanning Electron Microscopy (SEM) (morphology), Fourier Transform Infrared Spectroscopy (FTIR) (chemical structure) and TGA (thermal analysis). The membranes thickness was measured by digital micrometer. The fractions of base polymers and of the carrier D2EHPA were varied to determine the optimum composition with respect to extraction capability of the membranes. After optimization of the ph of the aqueous solution, the concentration of D2EHPA in the membrane, the concentration of the MB and the stirring speed, more than 93% extraction efficiency has been reached at ph = 6.0. The chemical formula of the complex (D2EHPA-MB) extracted by the PIMs was determined by the method of slopes Published by Elsevier Ltd. Selection and peer-review under responsibility of ISWEE 11 Open access under CC BY-NC-ND license. Keywords: Polymer Inclusion Membrane (PIM); D2EHPA; Extraction; cationic dye, Methylene Blue (MB). 1- Introduction: Dyes are widely used in various industries, such as textiles, paper, plastics, cosmetics and leather, for coloring their final products [1]. It is recognized that public perception of water is greatly influenced by the color. Color is the first contaminant to be recognized in wastewater [2]. The presence of very small amounts of dyes in water (less than 1 ppm for some dyes) is highly visible and undesirable [3]. Once the dye has contaminated the water, its removal by conventional wastewater treatment method is particularly difficult because many dyes are stable to light and oxidizing agent and are resistant to aerobic bio-oxidation [4]. In recent years several physico-chemical decolorization processes have been developed, such as membrane separation, electrochemical, flocculation coagulation, reverse osmosis, ozone oxidation, biological treatments, etc. [5]. Ultimately, a simple, cost effective and safe alternative for color removal and recovery of dyes from textile effluent is required and membrane technology may provide this alternative. Among membrane technologies, liquid membranes have acquired a prominent role for their use in separation, purification or analytical application in various areas, such as biomedicine, ion selective electrodes, effluent treatment and hydrometallurgy [6]. * Corresponding author. Tel.: ; fax: E-mai: kebiche_anissa@yahoo.fr Published by Elsevier Ltd. doi: /j.proeng Open access under CC BY-NC-ND license.

2 Aitali Salima et al. / Procedia Engineering 33 ( 2012 ) Muthuraman et al. [7,8] and Hu et al. [9] reported the recovery of dyes by liquid- liquid extraction. Membrane liquid have been developed for the extraction of dyes from wastewater. Some workers have studied the extraction of anionic and cationic dyes, from aqueous solutions by emulsion liquid membrane [10-12]. Removal of anionic reactive dyes from water using anion exchange membranes as adsorbers was reported by Liu et al [13], Wu et al.[14] have also used a cation exchange membranes for treating a water containing a cationic dye methyl violet 2B. Supported liquid membranes (SLM) have the advantage of achieving selective removal and concentration in single step. Thus having great potential for reducing cost significantly [15-17]. The separation of synthetic dye Rhodamine 6G (R6G) and water was investigated using blended organic liquids in a supported liquid membrane (SLM) extraction system [18]. The transport of cationic dyes methyl violet and Rhodamine B from aqueous synthetic dye solution through flat type SLM using Di (2- ethyl) phosphoric acid (D2EHPA) as carrier was studied by Hajrabeavi et al [19]. Vegetable oils were used such as carried natural in SLM for extraction of Rhodamine B [20] and astacryl golden yellow [21]. Supported Liquid Membranes (SLMs) are considered as an attractive alternative to conventional liquid liquid extraction, especially in the treatment of dilute solutions, because they combine the extraction and stripping processes in a single step. However, lack of long-term stability is the main drawback of the SLM process, although it has been reported that this stability can be reduced by the proper composition choice of the membrane phase [6]. Recently, a novel type of liquid membrane system, called a polymer inclusion membrane (PIM) has developed; PIMs are formed by casting cellulose triacetate (CTA) from an organic solution to form a thin stable film [22] Polymer inclusion membranes (PIMs) retain most of advantage of SLM while exhibiting excellent stability and versatility. The lower diffusion coefficient often encountered in PIMs can be easily offset by creating a much thinner membrane in comparison to its traditional SLM [23, 24]. Ozmen and Yilmaz have synthesized a membrane polymer using a B cyclodextrin and starch for the sorption of Congo red from aqueous solution. It was found that, the ph effects of the adsorption capacity and the effective ph range for the sorption is better at ph equal 4 to 8 [25]. Kyzas et al. [26] used the molecularly imprinted polymer (MIP) for the adsorption of a Reactive Red (RR) and basic red dye, MIPs were applied in four sequential cycles of adsorption- desorption with a limited loss of adsorption capacity only 10%. The aim of this study is to investigate polymer inclusion membranes (PIMs) consisting of plasticizer cellulose triacetate (CTA) and Di (2- ethyl) phosphoric acid (D2EHPA) as the carrier, for removing the cationic dye methylene blue from aqueous solution. The effects of time, ph, the stirring speed, concentration of the D2EHPA and dyes have been optimized. 1- Experimental 2-1- Reagent Cellulose triacetate (CTA), 2- Nitrophenyloctyl ether (2NPOE), Di(2- ethyl hexyl) phosphoric acid( D2EHPA) were obtained from Aldrich. Chloroform (CHCl 3 ) was acquired from Fluka. Methylene blue (basic blue 9) was purchased from Merck; the structure of this dye is given in Fig.1. The aqueous phases were prepared by dissolving the different reagents in distilled water. M= g/mol Fig. 1: The structure of methylene blue.

3 40 Aitali Salima et al. / Procedia Engineering 33 ( 2012 ) Polymer inclusion membrane preparation PIMs were prepared using the same procedure described by Kebiche-Senhadji et al. [27, 28]. A chloroform solution of CTA (200mg) in 20ml, the appropriate plasticizer (0.3ml) and the carrier (D2EHPA) in variable amounts were poured into a 9.0 cm diameter flat bottom glass Petri disk. The solvent was allowed to evaporate slowly overnight to obtain a polymer film. A small quantity of distilled water was deposited on the film to help its unstitching of the glass support Membrane characterization FTIR spectra were obtained using FTIR- 8400S of Shimadzu spectrophotometer; measures were taken in the range cm -1 with 4cm -1 resolution and 80 scans. Scanning electronic microscopy image and micro analyze of PIMs were acquired using a HITACHI S4500 microscope that can reach a resolution of 1.5nm. Thermogravimetric analyses were achieved using an apparatus of thermogravimetry of high resolution, TGA2350 (MT instruments) with a temperature going from ambient until 1000 C Membrane solid-liquid extraction Solid liquid extraction experiments were undertaken at fixed temperature and with stirred solution using a magnetic stirrer in rang of [ rpm]. Dilute HNO 3 and NaOH were used to adjust ph of aqueous solution. The wave length of maximum adsorption max of methylene blue was 650nm. The percentage extraction (E) and the distribution ratio (D) were calculated as per the following equation. E (%) [ dye ] aq 0 aqt = x100 (1) [ dye ] [ dye ] aq 0 D [ dye ] org = (2) [ dye ] aq Where [dye] aq0 : initial dye concentration in the aqueous phase ( mg/l). [dye] aqt : dye concentration aqueous phase after extraction ( mg/l). [dye] org : dye concentration in the organic phase ( membrane (mg/l)). 3- Results and discussion 3-1- Membrane characterization Several techniques were investigated to characterize the PIMs such as; FTIR, SEM and ATG FTIR Table 1 selects the peak values of the reference CTA, CTA+2NPOE and CTA+2NPOE+D2EHPA membranes. The obtained results showed the absorption bands located around 1740cm -1, which is attributed to stretching vibration of the carbonyl group. The IR spectra of the CTA exhibit weak bands at 2930 cm 1 attributed to the stretching modes of aliphatic CH groups. In addition, the absorption band at 1370 cm 1 is due to CH deformation of CH 3. The absorption band at 1740 cm 1 correspond to C=O (acetate) stretching. Two absorption bands at 1030 and 1210 cm 1 attributed to C O stretching mode are also observed. The peaks at 1525 and 1350 cm -1 correspond respectively to the stretching modes of N=O and C-N of 2NPOE. The bands at 1240 and 1020 cm -1 correspond respectively to the stretching modes of P=O and P-O bond of D2EHPA. This indicates that only weak interactions occur between constituents of the PIMs such as Van der Waals or hydrogen bonds.

4 Aitali Salima et al. / Procedia Engineering 33 ( 2012 ) Table 1: Peak values and the corresponding radical in different membranes Membrane Peak value( cm -1 ) Corresponding radical C-H 2950 C=O 1740 CTA C-H (deformation of CH ) C-O 1210 and 1030 CTA+2NPOE CTA+2NPOE+D2EHPA Same bands in addition to C-H C=O (CTA) NO 2 -CH 3 C-N -CH 2 P=O P-O SEM The SEM images of all membranes (Fig. 2) show uniform surfaces and appear dense with no apparent pores. (a) (b) (c) Fig.2 : SEM views of CTA membrane (a), CTA + 2-NPOE membrane (b) and PIM containing D2EHPA (c) (surface morphology).

5 42 Aitali Salima et al. / Procedia Engineering 33 ( 2012 ) TGA We used thermogravimetric analyses (TGA) to link specific temperature and height of mass changes to the degradation of a specific compound or fragment of it. Fig.3 shows thermogram (%weight loss vs. temperature) for the PIM (CTA+2- NPOE+D2EHPA). The thermogram of the PIM containing D2EHPA was somewhat different of the general trend; it was observed an absence of actual separation of the degradation steps attributed to individual components. The feature of the thermogram seems to indicate peculiar interactions between the components in the membrane; more details were given in a previews work [27]. Fig.3: Thermogram of PIM (CTA + 2-NPOE + D2EHPA) 3-2- Solid- liquid extraction Effect of the carrier concentration D2EHPA in the membrane is varying in this range of (5-30 mol/cm 2 ). The results of different carrier concentration are given in Fig. 4. The percentage of extraction increase with increase of carrier concentration up to 15 mol/ cm 2 then stabilized for the concentration higher. Fig. 4: Effect of D2EHPA concentration onto the extraction efficiency.

6 Aitali Salima et al. / Procedia Engineering 33 ( 2012 ) Effect of the ph in aqueous solution ph of the aqueous solution is one of important parameter which controls the process of extraction of dyes. To study the effect of ph on the extraction percentage of dye from the aqueous solution, ph is varied between 1 and 12, whereas D2EHPA concentration in PIM and dye in aqueous phase were kept constant. The relationship between the extraction efficiency and the ph is given in Fig. 5. The results show that the extraction of MB is highest at ph= 6± 0.2. These results indicate that the dye is extracted in cationic form, across the hydrophobic membrane with high value of the extraction efficiency. The measure of the final ph shows a decrease of two unite, which confirm that we have an exchange between H + of the D2EHPA and the of BM + (the cationic dye species form neutral ion pairs with the anionic carrier) Dye + aq +[RH 2 ] org [dye(rhr)] org + H + aq This result is comparable to that obtained by Drapala and Hajarabeevi [16, 19] Fig. 5: Effect of the ph of the aqueous solution onto the extraction efficiency Effect of stirring speed Fig.6 shows the influence of stirring speed on the extraction of the MB. The result indicates that extraction efficiency increase by increasing of speed, the optimum was obtained at 350 rpm. For the speed faster than 350 rpm the decrease of permeability is the consequence of the turbulence caused by stirring. The same result is obtained by Muturaman and Teng who studied the transport of RhodamineB (cationic dye) cross supported liquid membrane using vegetable oil as carrier [20]. Further research studies were done at 350 rpm.

7 44 Aitali Salima et al. / Procedia Engineering 33 ( 2012 ) Fig.6: Effect of the stirring speed onto the extraction efficiency of the cationic dye (MB) Effect of initial dye concentration The variation of the dye concentration at the optimum condition have been done over the rang [ ppm]. It s shown in Fig. 7 that the extraction of the cationic dye is constant in the interval [ ppm] the efficiency of extraction is average 67 %, after this value (250 ppm) a decrease of the extraction efficiency is noticed with the increase of the dye concentration. This may be due to membrane saturation and lower effective membrane area. This behavior has also been shown in several studies concerning a number of different metal carrier polymer membrane systems [28-30]. Fig. 7: Effect of the dye concentration onto the extraction efficiency 3-4- Determination of the complex form The curves of log D = f (ph f ) (Fig.8) and log D = f ([HR]) (Fig.9), give the composition and the complex formed methylene blue-d2ehpa, the curves have linear forms and show that the distribution coefficient (D) increase with increasing ph and D2EHPA concentration:

8 Aitali Salima et al. / Procedia Engineering 33 ( 2012 ) Log (D) = m ph f + (m=n) log [D2EHPA] org + log K m, n..(11) From the slop of the functions Log D = f (ph f ) and Log D = f ([HR]) we can determined directly the complex form extraction of dye with the PIM, then we can write: With: m = 1 and n = 0. MB + + (m + n) (HR) MBR m (HR) n The result suggests that the MB is extracted by the matrix (CTA-NPOE-D2EHPA) in the form: MB-R Fig. 8: Variation of log (D) versus the final ph of extraction Fig. 9: The variation of log (D) with the extractant concentration. 4- Conclusion: A simple and efficient method is presented for the recovery of a cationic (MB). The method is based on the use of a polymer inclusion membrane (PIM) containing Di(2-ethyl hexyl) phosphoric acid as extractant which transfers quantitatively MB species from an aqueous feed phase into a solid organic phase (PIM). The efficiency of the method depends on various parameters, i.e. the ph of the aqueous phase, the quantity of the extractant in the membrane, the initial dye concentration and the stirring speed. Under optimum conditions, an almost quantitative (93%) recovery of methylene blue is achieved. The cationic dye is extracted by the matrix (CTA-NPOE-D2EHPA) in the form: MB-R. The characterization of membrane resumes that only weak interactions between constituents of the PIMs such as Van der Waals or hydrogen bonds. These results are very promising and we are also complete the study by the facilitated transport operation. References [1] Lin JX, Zhan SL, Fang MH, Qian XQ, Yang H. Adsorption of basic dye from aqueous solution onto the ash. Journal of Environmental Management 2008; 87: [2] Crini G. Non conventional cow- cost adsorbents for dye removal: A Review. Bioresource Technology 2006; 97: [3] Robinson T, McMullan G, Marchant R, Nigam P. Remediation of dyes in textile effluent a critical review on current treatment technologies with a proposed alternative. Bioresource technology 2001;77: [4] Ramesh B, Parande AK, Raghu S, Kumar TP. Textile Technology. Cotton textile pressing: Waste generation and effluent treatment. Journal of cotton science 2007; 11: [5] Sanghi R, Bhattacharya B. Review on decolorisation of aqueous dye solutions by low cost adsorbents. Coloration Technology 2002; 118:

9 46 Aitali Salima et al. / Procedia Engineering 33 ( 2012 ) [6] Muthuraman G, Palanivelub K, Teng TT. Transport of cationic dye by supported liquid membrane using D2EHPA as the carrier. Coloration Technology 2010; 126: [7] Muthuraman G, Teny TT. Extraction and recovery of rhodamine B, methyl violet and methylene blue from industrial wastewater using D2EHPA as an extractant. Journal of Industrial and Engineering Chemistry 2009; 15: [8] Muturaman G, Teng TT, Leh CP, Norli I. Extraction and recovery of methylene blue from industrial wastewater using benzoic acid as an extractant. Journal of Hazardous Materials 2009; 163: [9] H. Hu, M. Yang. J. Dang, Treatment of strong acid dye wastewater by solvent extraction, Separation and Purification Technology 42(2005) [10] Daas A, Hamdaoui O. Extraction of anionic dye from aqueous solution by emulsion liquid membrane. Journal of Hazardous Materials 2010;178: [11] Djenouhat M, Hamdaoui O, Chiha M, Samar M. Ultrrasonication- assisted preparation of water- in oil emulsion and application to the removal of cationic dyes from water by emulsion liquid membrane. Part 2. Permeation and stripping. Separation and purification technology 2008; 63: [12] Das C, Rungta M, Arya G, Gupta SD, De S. Removal of dyes and their mixture from aqueous solution using liquid emulsion membrane. Journal of Hazardous Materials 2008; 159: [13] Liu CH, Wu JS, Chiu HC, Suen SY, Chu KH. Removal of anionic reactive dyes from water using anion exchange membranes, as adsorbers. Water Research 2007; 41 : [14] Wu JS, Liu CH, Chu KH, Suen SY. Removal of cationic dye methyl violet 2B from water by cationic exchange membranes. Journal of Membranes Sciences 2008; 309: [15] Yang XJ, Fane AG, Naughtan M. Removal and recovery of heavy metals from wastewater by supported liquid membrane. Water Science Technology 2001; 43: [16] Drapala A, Dzygiel P. Jonsson JA, Wieczorek P. Supported liquid membrane of peptides. Acta Biochimica Polonia 2001; 48 : [17] Yourd ER, Tyson J F. Comparison of supported liquid membranes and solid phase extraction for quantitative removal of lead from aqueous solutions. Canadian Journal of Chemistry 2003; 81: [18] Nisola GM, Cho E, Belton AB, Han M, Kim Y, Chung WJ. Dye/ water separation through supported liquid membrane extraction. Chemosphere 2010; 80: [19] Hajrabeavi N, Bilal LM, Easwramoorthy D, Palanivelu K. Facilitated transport of cationic dyes through a supported liquid membrane with D2EHPA as carrier. Desalination 2009; 245: [20] Muthuraman G, Teng TT. Use of vegetable oil in supported liquid membrane for the transport of RhodamineB. Desalination 2009; 249: [21] Muthuraman G, Palanivelu K. Transport of textile dye in vegetable oil based supported liquid membrane. Dye and Pigments 2006; 70: [22] Kozlowski CA, Kozlowska J, Pellowski W, Walkowiak W. Separation of Cobalt 60, Strontium 90, and Cesium-137 radioisotopes by competitive transport across polymer inclusion membranes with organo phosphorous acids. Desalination 2006; 198: [23] Arous O, Kerdjoudj H. Seta P.Comparison of carrier facilitated silver (II) and Copper (II) ions transport mechanisms, in a supported liquid membrane and in a plasticized cellulose triacetate membrane. Journal of Membrane Science 2004; 241: [24] Nghiem LD, Mornane P, Potter ID, Perera JM. Extraction and transport of metal ions and small organic compounds using polymer inclusion membranes (PIMs). Journal of Membrane Science 2006; 281: 7-4. [25] Ozmen EY, Yilmaz M. Use of cyclodextrin and starch based polymer for sorption of Congo red from aqueous solutions. Journal of hazardous materials 2007; 148: [26] Kyzas GZ, Bikiaris DN, Lazaridis NK. Selective separation of basic and reactive dyes by molecularly imprinted polymer (MIP)s. Chemical Engineering Journal 2009; 140: [27] Kebiche-Senhadji O, Mansouri L, Tingry S, Seta P, Benamor M. Facilitated Cd(II) transport across CTA polymer inclusion membrane using anion Aliquat 336 and cation D2EHPA metal carrier. Journal of Membrane Science 2008; 310: [28] Kebiche-Senhadji O, Tingry S, Seta P, Benamor M. Selective extraction of Cr(VI) over metallic species by polymer inclusion membrane (PIM) using anion (Aliquat 336) as carrier. Desalination 2010; 258: [29] Kozlowski CA, Walkowiak W. Removal of chromium (VI) from aqueous solutions by polymer inclusion membranes. Water Research 2002; 364: [30] Walkowiak W, Bartsch RA, Kozlowski C, Gega J, Charewicz WA, Amiri-Eliasi B. Separation and Removal of Metal Ionic Species by Polymer Inclusion Membranes. Journal of Radioanalytical and Nuclear Chemistry 2000; 246:

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