A Batch Adsorber Design for Rhodium Adsorption on Pyrogallol Formaldehyde Resin

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A Batch Adsorber Design for Rhodium Adsorption on Pyrogallol Formaldehyde Resin 1 Mustafa Can 1 Vocational High School of Arifiye, 54580, Sakarya University, Turkey Abstract: The adsorption of rhodium (III) ions onto pyrogallol formaldehyde nano resin (PGNR) in a batch adsorber has been studied. Adsorption experiments were carried out by agitating 0.2g PGNR with 50 ml of Rh (III) ion solution of the initial concentrations from 19 to 95 mg/l. A contact time of 60 min was required to achieve equilibrium. At the end of the adsorption period, 15 ml sample was centrifuged and concentration was measured using AAS. The experimental isotherm data were analyzed using the Langmuir, Freundlich and Temkin equations. Isotherm parameters for three equations were determined and discussed. Adsorption of Rh (III) onto PGNR followed the Langmuir isotherm. The monolayer adsorption capacity is 66.27 mg/g. A single stage batch adsorber was designed for different adsorbent mass/treated effluent volume ratios using the Langmuir isotherm. Key words: batch adsorber, sorption kinetics, rhodium, pyrogallol, resol resin. 1. Introduction Rhodium containing wastes has become a source of recycle because its low ore reserves and high utilization. It is difficult to follow the fate of metallic ions after they enter and pollute the ecosystem as they move from one ecological trophic layer to another [1]. Only few scientists have studied adsorption of rhodium ions onto various adsorbents. Reports include studies by Morisida at al, who investigated the rhodium (III) adsorption of the amine modified tannin polymer [2,3]; Akkaya at al studied the adsorption of rhodium (III) onto poly(1,8-diaminonaphthalene) [4]; Ogata at al designed an adsorber onto gibbsite [5]; Alam et al. studied the adsorption of Rh (III) onto various ion exchange resins [6]; Moon et al. studied the sorption of Rh(III) onto Amberlite XAD-4 impregnated with Aliquat 336 [7]; Couceiro et al. studied adsorption and desorption kinetics Rh (III) and Pt (IV) in turbid suspensions [8]; Sako at al studied the adsorption and surface complexation modeling of Rh (III), Pd (II) and Pt (IV) onto semi-arid soils and sediment [9]; Ogata at al designed an adsorber onto gibbsite [5]; However, until now, as far as we can find, there isn t any report involving rhodium adsorption system design especially for batch systems involving polymer based adsorbents. This paper presents mathematical models developed for predicting the optimized minimum operating time for the removal of specified amounts of Rh (III) ions from a fixed volume of solution using a novel pyrogallol derived resol nano resin (PGNR) particles [10]. Data used for developing these models were obtained from batch kinetic studies of the adsorption Rh (III) ions *Corresponding author: Address: Vocational School of Arifiye, Sakarya University, 54580, Arifiye, Sakarya TURKEY. E-mail address: mstfacan@gmail.com, Phone: +902642953357 Fax: +90264 295 72 02

M. CAN / ISITES2014 Karabuk - TURKEY 951 using the PGNR adsorbent. Both single stage adsorber models were used on the data. 2. Materials and Method RhCl 3. 3H 2 O and HCl purchased from Merck Company. AAS standard solutions for determination of PGM purchased form UltraScientific Company. All other reagents were analytical grade. Preparation of PGNR polymer was explained in detail at our recent publication dealing synthesis and characterization of polymer [10]. The aqueous Rh (III) stock solution was prepared from solid RhCl 3.3H 2 O in 0.1 M HCl. Subsequently ph and pcl adjusted at 4.5 and 3, respectively. The Rh (III) solutions were prepared by dilution with ultra-pure water (Milli-Q, UK). The rhodium (III) solution was prepared by diluting stock solutions to desired ph and pcl concentrations at 4.5 and 3, respectively. All adsorption experiments were carried out in a standard and strictly adhered to batchwise system. At the end of the adsorption period, 15 ml samples were centrifuged and the solutions were filtered through a 0.45 μm Milipore filter paper to avoid any solid particle in the aqueous phase. Samples were measured using AAS. All the adsorption tests were performed at least twice so as to avoid wrong interpretation owing to any experimental errors. FAAS calibrated using 0, 4, 12 and 20 ppm standard solution for Rh (III) in 1M HCl. Samples diluted to measurement limits for precise results. Amount of adsorbed metal ions was calculated from the concentrations in solutions before and after adsorption process. Results were taken from the average of three scans for each sample. The amount of metal adsorbed onto PGNR, qe (mg/g), was calculated as follows: ( ) (1) where C 0 and C t are the initial and time t liquid-phase concentrations of the metal (mg/l), respectively. V the volume of the solution (L) and W the weight of the dry PGNR used (g). Each experiment was performed twice at least under identical conditions. Twice tests showed that the standard deviation of the measurement was ±2.5%. 3. Results Adsorption isotherms can be used to predict the design of single-stage batch adsorption systems and it is already been described by Ho and McKay [11]. Based on the best fitting isotherm, a single stage adsorber as shown in Figure 1 was designed for different solution volumes. The design objective is to reduce the rhodium (III) solution of volume V, L from an initial metal concentration of C 0 C 1 (mg/l). The amount of adsorbent is M and the solute loading on the adsorbent changes from q 0 (mg/g) to q 1 (mg/g). At time t = 0, q 0 = 0 and as time proceeds the mass balance equated the rhodium adsorbed from the liquid to that picked up by the solid. The mass balance equation for the sorption system in Figure 1 can be written as equation ( ) ( ) (1) When system reaches to the equilibrium, and will change to and, respectively.

M. CAN / ISITES2014 Karabuk - TURKEY 952 M, m of adsorbent q 0, mg of solute/g of adsorbent V (L of solvent) C 0 (mg of solute/l of solvent) Batch V (L of solvent) C 0 (mg of solute/l of solvent) M, m of adsorbent q e, mg of solute/g of adsorbent Figure 1. Schematic representation of the single stage batch adsorber system. From adsorption studies and from model results it was seen that the Langmuir model gave a more robust fit to equilibrium data from PGNR particles [12]. Langmuir constants used further calculations can be seen at Table 1. On this basis, the Langmuir isotherm equation was used to predict the amount of PGNR particles required to remove a certain percentage of Rh (III) from various volumes of solutions. With Since the equilibrium studies confirm that the equilibrium data for Rh (III) onto PGNR particles follows a Langmuir isotherm equation (2) substituted with q e in equation (1) and it can be rearranged as [ ] ( ) ( ) Table 1. Langmuir isotherm constants for Rh (III) adsorption onto PGNR particles. a L Isotherm K L (L/g) (L/mg) (mg/g) R L r 2 Lineweaver-Burk linear 0.1623 0.0011 66.27 0.973-0.876 0.99989 Q max

M (g) M (kg) M. CAN / ISITES2014 Karabuk - TURKEY 953 100000 90000 80000 70000 60000 50000 40000 30000 20000 10000 0 0 0 50 100 0 20 40 60 (a) V (m 3 ) (b) C 0 (g/m 3 ) Figure 2. (a) Adsorbent mass (M) against volume of effluent (V) treated for various percentage of rhodium (III) removal at 100 g/m 3 initial the rhodium ion concentration. (b) Adsorbent mass (M) against initial Rh (III) concentration for 90% metal removal at various volume of solutions (V) treated. 4. Discussion Figure 2 (a) shows a series of plots derived from Equation (3) for the adsorption of the Rh (III) ions onto PGNR. An initial metal ion concentration of 100 g/m 3 is assumed and Figure 2 shows the required amount of sawdust to reduce the color content by 75%-99% at various volumes of solutions. For a single-stage adsorption system, thus the adsorbent demonstrated adsorption capacity of the metal ions containing solutions. For example, 1 m 3 of solution is to be treated. The required masses of PGNR are 31, 41, 58, 92, 193 and 997 g of solution containing 100 g/m 3 Rh (III) at 293 K for 75%, 80%, 85%, 90%, 95%, and 99% rhodium removal, respectively. Figure 2 (b) shows the required amount of PGNR to reduce the rhodium ion content by 90% at various volumes of solutions which have different Rh (III) concentrations. For example, 5 m 3 of solution is to be treated, the required amounts of PGNR to reduce the rhodium ions content by 90% increased from 905 to 912 kg with increase in the initial Rh (III) concentration from 0,1 to 50 g/m 3. The amount of PGNR required to remove 90% of rhodium ions from aqueous solution can be predicted for any initial Rh (III) concentration for a fixed volume of effluent (V). Through such a projection, a real single stage adsorption system can be designed. Conclusions 75% 80% 85% 90% 95% 99% 10000 In this study, mathematical model were applied for the adsorption of Rh (III) onto PGNR particles using Langmuir isotherm data obtained experimentally via batch processes. The data from single-stage optimization models suggest that it will be useful for the design of adsorption plant for large-scale adsorption of Rh (III) by PGNR particles from recycling streams. It is not feasible to removing 95% of Rh (III) ions in single-stage process. Pilot studies using this 9000 8000 7000 6000 5000 4000 3000 2000 1000 0,1 m3 0,5 m3 1 m3 5 m3 10 m3 20 m3 30 m3 40 m3 50 m3 100 m3

M. CAN / ISITES2014 Karabuk - TURKEY 954 adsorbent are in progress to ascertain its full potential in the treatment of wastewater. Acknowledgements Collate acknowledgements in a separate section at the end of the article before the references and do not, therefore, include them on the title page, as a footnote to the title or otherwise. List here those individuals who provided help during the research (e.g., providing language help, writing assistance or proof reading the article, etc.). References 1 Unuabonah EI, Adebowale KO. Optimization of kinetic data for two-stage batch adsorption of Pb(II) ions onto tripolyphosphate-modified kaolinite clay. Journal of Chemical Technology & Biotechnology. 2009;84(11):1726 1735. 2 Morisada S, Rin T, Ogata T, Kim YH, Nakano Y. Adsorption recovery of rhodium(iii) in acidic chloride solutions by amine-modified tannin gel. Journal of Applied Polymer Science. 2012;126(s2):E34 E38. 3 Can M. Biomaterials derived from Renewable Resources for the Recovery of Precious Metals. Research Journal of Chemistry and Environment. 2013:1-3. 4 Akkaya T, Gülfen M, Olgun U. Adsorption of rhodium(iii) ions onto poly(1,8- diaminonaphthalene) chelating polymer: Equilibrium, kinetic and thermodynamic study. Reactive and Functional Polymers. 2013;73(12):1589 1596. 5 Ogataa F, Iwataa Y, Kawasakia N. Adsorption of rhodium(iii) from plating solutions by calcined gibbsite. Toxicological and Environmental Chemistry. 2013;95(6):890-898. 6 Alam MS, Inoue K, Yoshizuka K. Ion exchange/adsorption of rhodium(iii) from chloride media on some anion exchangers. Hydrometallurgy. 1998;49(3):213 227. 7 Moon JK, Han YJ, Jung CH, Lee EH, Lee BC. Adsorption of rhenium and rhodium in nitric acid solution by Amberlite XAD-4 impregnated with Aliquat 336. Korean Journal of Chemical Engineering. 2006;23(2):303-308. 8 Couceiro F, Turner A, Millward GE. Adsorption and desorption kinetics of rhodium (III) and platinum (IV) in turbid suspensions: Potential tracers for sediment transport in estuarine flumes. Marine Chemistry. 2007;107(3):308 318. 9 Sako A, Lopes L, Roychoudhury AN. Adsorption and surface complexation modeling of palladium, rhodium and platinum in surficial semi-arid soils and sediment. Applied Geochemistry. 2009;24(1):86-95. 10 an M, ulut, acar M. ynthesis and characteri ation of pyrogallol-formaldehyde nano resin and its usage as adsorbent. Journal of Chemical & Engineering Data. 2012;57(10):2710 2717. 11 McKay G, Otterburn MS, Aga JA. Fuller's earth and fired clay as adsorbents for dyestuffs.

M. CAN / ISITES2014 Karabuk - TURKEY 955 Water, Air, & Soil Pollution. 1985. 12 Can M. Rhodium Adsorption on Gallic Acid Resol Resin. Acta Physica Polonica A. 2014.