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Water SA

On-line version ISSN 1816-7950

Water SA vol.35 n.5 Pretoria Oct. 2009

 

Cyclodextrin-ionic liquid polyurethanes for application in drinking water treatment

 

 

TJ Malefetse, BB Mamba*; RW Krause and MM Mahlambi

University of Johannesburg, Department of Chemical Technology, PO Box 17011, Doornfontein 2028, South Africa

 

 


ABSTRACT

The prevalence of toxic contaminants in water remains a huge challenge for water-supplying companies and municipalities. Both organic and inorganic (especially heavy metals) pollutants are often present in water distribution networks. The presence of these contaminants in drinking water poses a major risk to human health. Organic and inorganic pollutants often co-occur in drinking water networks. However, at present there is no water treatment intervention that simultaneously removes both organic and inorganic pollutants from water to desirable levels. In our laboratories, recent studies have shown that both functionalised and un-functionalised cyclodextrin (CD) polymers are capable of removing organic pollutants from water, with the functionalised CD polymers showing an enhanced absorption capability. Ionic liquids (ILs), on the other hand, have been reported to absorb heavy metals from aqueous media. In this paper, we report on the synthesis of several cyclodextrin-ionic liquid (CD-IL) polymers, a dual system capable of removing both organic and inorganic pollutants from water. This system has been tested and has proved to possess excellent capabilities for the removal of model pollutants such as p-nitrophenol (PNP), 2,4,6-trichlorophenol (TCP) and chromium (Cr6+) from aqueous media.

Keywords: organic and inorganic pollutants, CD polymers, ionic liquids, CD-IL polymers


 

 

Introduction

Organic and inorganic water pollutants pose a major threat to human health even when present at low concentrations. For instance, because organic pollutants persist in the environment for long periods of time, they can be absorbed by plants thereby finding their way to poisoning the food chains of living organisms (Oleszczuk et al., 2004). They have also been linked to adverse human effects such as cancer, nervous system damage, reproductive disorders, as well as the disruption of the immune system (EPA, 2006). Also, organic contaminants released in one part of the world can be transported globally via oceans and atmospherically, and their effects can be felt in regions which are distant from where they originate.

On the other hand, inorganic pollutants, particularly heavy metals such as lead, cadmium, mercury and silver, have been reported to be toxic and even lethal to the human body, especially the central nervous system (Morales et al., 1999). These metals have a great affinity for sulphur and hence attack the sulphur bonds of enzymes causing them to malfunction (Lewis et al., 2001; Morales et al., 1999). One of the primary sources of heavy metal pollution in developing countries is industrial discharge. Taking into consideration the toxicity and the bioaccumulation of organic and inorganic pollutants, even in drinking water networks, a technique that can simultaneously remove both inorganic and organics from water needs to be developed. In this paper, we thus report on a technique that utilises cyclodextrin-ionic liquid (CD-IL) polymers for the simultaneous quenching of these pollutants from drinking water.

Cyclodextrins (CDs), first discovered by Villiers in 1891, are cyclic oligomers formed by the enzymatic hydrolysis of starch by Bacillus macerans (Szeitjli, 1998). The three most commonly known CDs contain 6 (α), 7 (β) and 8 (γ) glucose units which are linked together by α-(1,4) linkages (Bender and Komiyana, 1978). Liu et al. (2003) reported that CDs have a non-polar cavity which provides a micro-environment for the encapsulation of non-polar, low molecular weight compounds (formation of an inclusion complex) (Scheme 1).

 

 

However, CDs are slightly soluble in water which limits their sole application for water treatment purposes. This necessitates the functionalisation and, in particular, polymerisation of the parental CDs with suitable bi-functional linkers such as hexamethylene diisocyanate (HDI) and toluene diisocyanate (TDI) to make them insoluble (Li and Ma, 1999). These water-insoluble cyclodextrin polymers have been successfully synthesised in our laboratories and have been found to be effective in the absorption of organic pollutants at very low (ng·ℓ-1) concentrations (Mhlanga et al., 2007; Mamba et al., 2007). Also, mono-functionalised insoluble CD polymers were found to be effective in the removal of toxic phenolic compounds from the aqueous media at very low concentrations (Mamba et al., 2007). Trichloroethylene was removed to non-detectable levels whilst PNP was removed from a 10 mg·ℓ-1 spiked water sample with a removal efficiency of 99% (Salipira et al., 2007). During functionalisation, incorporation of specific functional groups can decrease the solubility of CDs, increase their stability in the presence of light, heat and oxidising conditions, or decrease their volatility (Szeitjli, 1998; Harada, 1997).

Ionic liquids (ILs) have aroused increasing interest for their promising role as alternative media for volatile solvents (Wei et al., 2003). ILs are defined as salts with a low melting point composed of organic cations and mostly inorganic anions such as Cl-, Br-, [PF6]- and [BF4]- (see Fig. 1). Besides anions such as hexafluorophosphate, tetrafluoroborate and halide anions, other common inorganic anions that are used for the preparation of ILs are [SbF6]- and [(CF3SO2)2N]-. The anion need not necessarily be inorganic; ILs possessing organic anions such as alkylsulphate, tosylate and methanesulfonate are known. The most common types of organic cations are the imidazolium and pyridinium ions (Pereiro et al., 2007). Other less common cations include ammonium, phosphonium, pyrrolidinium and sulphonium cations.

 

 

Ferreira et al. (2000) reported that the forces of attraction between the cation and the anion are not sufficiently strong enough to hold them together as solids at ambient temperatures hence it is possible, by proper choice of starting material, to synthesise ionic liquids that are liquid at or below room temperature. ILs possess unique physical properties such as negligible vapour pressure, an ability to dissolve a wide range of organic and inorganic material, high thermal stability (for example, some ILs are liquid at 400ºC, while others are liquid at -96ºC) as well as variable viscosity and miscibility with water and other organic solvents (Liu et al., 2003; Liu et al., 2005; Welton, 1999). However, the most important property of ionic liquids that has been exploited in this study is their ability to extract metals from aqueous media (Cruz, 2000; Liu et al., 2005). In this regard, Visser et al. (2002) have reported the successful extraction of cadmium (Cd2+) and mercury (Hg2+) from an aqueous medium using ionic liquids via the formation of an IL-metal complex.

Since water-insoluble CD polymers have demonstrated the ability to absorb organic pollutants from water even at ng·ℓ-1 levels and on the other hand ILs are able to remove metal ions from water, these properties have therefore been combined by preparing polymers that are capable of removing both organic and inorganic contaminants from drinking water. The polymers are accessed via an initial functionalisation of a CD with an ionic liquid skeleton. Functionalisation of CDs mainly occurs at the hydroxyl groups located at C-2, C-3, and C-6 positions. In this study, CDs were functionalised at the C-6 (primary hydroxyl group) position with a tosyl group or halogen (Zhong et al., 1998). Both the tosylated and halogenated CDs provided access to a variety of CD-IL complexes. Upon reaction with bi-functional linkers (HDI and TDI), the CD-IL complexes produced the corresponding water-insoluble polymers (Fig. 2).

 

 

To the best of our knowledge, there is no known technique that simultaneously removes organic and inorganic contaminants from water. This paper reports on the synthesis and applications of water insoluble CD-IL polymers in the removal of model pollutants (PNP, TCP and Cr6+) from water.

 

Experimental

Materials

Unless otherwise specified, all chemicals were obtained from suppliers and used without further purification. All reactions were performed under inert conditions using argon or nitrogen pressure. N,N-dimethylformamide (DMF) was dried over calcium hydride for two days and then distilled under reduced pressure over calcium sulphate before usage. The p-toluene sulphonic anhydride was prepared according to literature procedure (Gao et al., 1995) and used without further purification.

All reactions were monitored by thin layer chromatography (TLC). TLC analysis was performed on aluminium sheets pre-coated with a 0.25mm layer of silica F254. The eluant used for the TLC analysis of CD derivatives, i.e. mono-6-deoxy-6-β-cyclodextrin tosylate (CDOTs), mono-6-iodo-6-β-cyclodextrin iodide (CDI) and CD-IL complexes was 5:4:3 butanol/ ethanol (95%) / water. TLC spots were visualised under an ultraviolet lamp (254 nm and/or 365 nm) or dipped in 5% sulphuric acid (H2SO4) in ethanol followed by heating on a hot-plate.

Instrumentation

A Midac FT-IR 5000 spectrophotometer was used for all infrared (IR) spectral measurements. IR data are listed with characteristic peaks in wave number (cm-1). The identity of the compounds was confirmed using NMR spectroscopy whose spectra were recorded at 300 MHz using a Varian Gemini 2000 spectrometer. Proton and carbon chemical shifts are reported in mg·ℓ-1 using the residual signal dimethyl sulphoxide (DMSO-d6) (δ = 2.49 for 1H and 39.50 for 13C) or trimethyl silane (TMS) (δ = 0) as an internal reference. For ultraviolet (UV) experiments, a UV-Visible Cary 50 Spectrophotometer was used for the collection of data. A Varian CP-3800 gas chromatograph ion-trap Saturn 2000 Mass Spectrometer was used for the quantification of organic pollutants. The GC was equipped with a Chrompac CP Sil 8 CB, 30m × 0.25 mm column with an internal diameter of 0.25 µm. A Varian Spectr Atomic Absorption 10 flame spectrophotometer (AAS) was used for the analysis of heavy metal ions. The AAS wavelength was set at 357.9 nm for the analysis of Cr6+ and a flame of air/acetylene was employed.

Synthesis of CD-IL complexes

The CD-IL complexes were synthesised from CDOTs and CDI. Due to the ease of formation of the mono-tosylate and ease with which the tosyl leaving group can be replaced, mono-tosylated cyclodextrins are generally good precursors for derivatives of CDs (Zhong et al., 1998). To prepare the CD-IL derivatives, an alkyl imidazole (10 molar equiv.) was added drop-wise to a stirred solution of either β-CDI or β-CDOTs (0.88mmol) dissolved in anhydrous DMF (40 mℓ). Stirring was continued at elevated temperatures (80ºC and 90ºC for β-CDI an β-CDOTs, respectively) under nitrogen for a further 24 h. After cooling to room temperature, acetone (25 mℓ) was added to precipitate the product. The reaction mixture was then stirred for 30 min. Evaporation of organic solvents using a rotary evaporator produced a white solid. This solid was finally dissolved in deionised water (50 mℓ) and precipitated by the addition of acetone (200 mℓ). The precipitate was filtered off and dried under vacuum to yield a white powdery solid.

Synthesis of CD-IL polymers

The CD-IL complexes in the above section (both tosylate and iodide derivatives) were reacted with bi-functional diisocyanate linkers, hexamethylene diisocyanate (HDI) and toluene-2,4-diisocyanate (TDI), to produce CD-IL polymers. Typically, the β-CD-IL complex (0.88 mmol) was dissolved in DMF (20 mℓ) and the bi-functional linker was added drop-wise to the reaction mixture. The solution was allowed to react at 75ºC for 18 to 24 h with constant stirring. The polymerisation reaction was monitored by IR spectroscopy. The completion of the polymerisation was confirmed by the total disappearance of the isocyanate peak at 2 270 cm-1 after 18 to 24 h (Li and Ma, 1999). The reaction mixture was then precipitated by the addition of acetone (100 mℓ). The solid formed was then left to settle in acetone for 10 min to allow for the removal of residual DMF from the polymers. To remove traces of DMF which might still be present, the polymers were filtered and washed with copious amounts of acetone (100 mℓ). The polymers were then dried overnight under reduced pressure.

The polymers under investigation were derived from the tosylate and iodide derivatives of β-cyclodextrin methyl imidazolium, β-cyclodextrin butyl imidazolium and β-cyclodextrin pyridinium precursors.

Preparation of para-nitrophenol (PNP), 2,4,6-trichlorophenol (TCP) and Cr6+ standards

Potassium dichromate, p-nitrophenol and 2,4,6-trichlorophenol were purchased from suppliers and used without further purification. PNP standards of 2, 5, 10, 15 and 20 µg·ℓ-1 were prepared and used to test the absorption efficiencies of the polymers in the absorption of organic pollutants from water. UV-visible spectroscopy was used to determine the amount of the pollutant absorbed by the polymers. A 10 mm cuvette cell was used as a sample holder. For the analysis of TCP, standards of 1, 2, 5, 10, 15 and 20 µg·ℓ-1 were prepared.

Gas chromatograph-mass spectrometry (GC-MS) was used for the analysis of TCP absorbed by the polymers; 2,4,6-trichlorophenol (10 mg·ℓ-1) was passed through the polymers and the filtrate was analysed for the residual amount of TCP using GC-MS. Solid-phase extraction (SPE) was employed to extract TCP from the filtrate. The extractant from SPE analysis was concentrated to about 2 mℓ by bubbling through nitrogen gas.

To analyse for the amount of Cr6+ absorbed by the polymers, atomic absorption spectrophotometer (AAS) was employed. Cr6+ standards of 2, 4, 5, 6 and 8 µg·ℓ-1 were prepared and used to determine the absorption efficiencies of the polymers. A Cr6+ concentration of 5 mg·ℓ-1 was chosen based on the detection limit of chromium by the AA instrument that was used (1 to 20 mg·ℓ-1).

Typically, 30 mℓ (10 mg·ℓ-1) of the pollutant was passed through the polymers (300 mg). GC-MS, AA and UV measurements were done before and after the spiked water samples have been passed through the polymers. A calibration curve was plotted in order to determine the amount of the spiked pollutants absorbed by the polymers.

 

Results and discussions

The results obtained after passing water containing PNP, TCP and chromium through the polymers are summarised in Table 1.

 

 

UV-visible spectroscopy results

Phenolic compounds are quite prevalent as pollutants in most aquatic systems; PNP was thus selected as a model pollutant. Furthermore, PNP can be analysed by UV spectroscopy since it has chromophores (i.e. covalently bonded but unsaturated groups such as NO2, C=C and C=O) that absorb electromagnetic radiation in the ultraviolet and visible regions of the spectrum (Field et al., 1995). Thus PNP strongly absorbs at λ = 318 nm (visible region of the spectrum). The PNP-spiked water samples that passed through the polymers were measured by UV spectroscopy and using the absorbance, the residual PNP concentration was determined using the calibration curve and the results are shown in Table 1.

It is evident from Table 1 that the CD-IL polymers that were synthesised have generally higher absorption efficiencies for organic pollutants when compared with the native β-CD/HDI and β-CD/TDI polymers. For example, absorption of up to 80% was recorded for the β-CDMIMOTs/HDI polymer. This is substantially higher than the respective 64% and 68% observed for the CD/HDI and CD/TDI native polymers. It should also be noted that the extraction efficiency of the imidazolium-based polymers is generally superior to those of pyridinium-based polymers. In fact, the extraction efficiency of 15%, which was recorded for β-CDPYROTs/HDI, is even lower than that of the native polymers.

GC-MS results

TCP-spiked water samples were passed through the polymers and it was observed that a substantial amount of the TCP was absorbed by the polymers. However, the amount of TCP absorbed by the polymers was found to be less than that absorbed for PNP. These polymers were therefore found to have higher affinity for PNP than TCP (Table 1). This may be attributed to the structure of these 2 compounds; the structure of compounds (compatible geometry) determines the amount of the compound that will fit in the cavity (Linde et al., 2000). TCP is highly branched and could not perfectly pack in the CD cavity while the structure of PNP renders it more amenable to the absorption sites of the β-CD-IL polymers resulting in higher removal efficiency of PNP than TCP. However, these polymers still showed high absorption efficiencies when compared to the native CD polymers. This implies that the incorporation of the imidazolium ring onto the CD backbone resulted in an enhancement of absorption efficiency by the polymers.

AAS results

Besides being readily available in our laboratories, chromium was chosen because it is a toxic inorganic pollutant (heavy metal) especially when present in water as Cr6+. This metal ion can penetrate the skin causing irritation, liver and kidney damage as well as a decrease in male sperm counts (Morales et al., 1999). AAS analysis of the eluant after passing the Cr6+ containing water samples demonstrated that the CD-IL polymers were able to remove Cr6+ with an absorption efficiency of up to 100%. This observation suggests that the IL component incorporated onto the CD backbone was still highly active in the extraction of heavy metals from water. It is noteworthy that the native β-CD polymers also absorbed Cr6+ from water. Similar studies (Cardas et al., 2005; Brusseau et al., 1997) have also revealed that native CD polymers indeed form complexes with heavy metal ions. Results for the extraction of Cr6+ using the native polymers as well as the CD-IL polymers are summarised in Table 1.

Effect of the type of the cation – imidazolium vs. pyridinium

As shown in Table 1, incorporation of the imidazolium ring onto the CD backbone generally favours the absorption of both PNP and TCP by the polymers. On the contrary, the pyridinium-based polymers are far much better at the extraction of TCP. Although the IL component also enhances the complexation of Cr6+ ions, due consideration must be given to the type of anion.

Effect of the alkyl chain length attached to the imidazolium ring: methyl vs. butyl

Previous studies (Visser et al., 2001; Pandey, 2006) suggest that the amount of pollutant absorbed is affected by the length of the alkyl chain attached to the imidazolium ring. These reports stated that the longer the alkyl chain, the less effective the ionic liquid for metal ion extraction. Our investigation seems to support a decrease in the amount of the pollutant absorbed when the alkyl chain is extended. As shown in Table 1, the methylimidazolium polymers were found to possess higher extraction efficiency compared to their butylimidazolium counterparts.

Effect of the type of anion – tosylate vs. iodide

A study of the effect of the counter-anion (tosylate and iodide) on the absorption efficiency of the polymer revealed no correlation between the amount of organic pollutant (TCP and PNP) absorbed and the type of anion present in the polymer. However, for the absorption of Cr6+, the tosylated polymers had high absorption efficiencies compared to the iodinated polymers. The tosylate anion is hydrophobic and thus enhances the chelation (hexavalent dentition) of the chromium with the cationic component of the CD-IL polymers. The tosylate anion enhances the chelation of the heavy metal by repelling the water molecules from the cationic component. The iodide anion is, on the other hand, a hydrophilic anion and has the opposite effect. This observation is in agreement with reports by Welton (1999) and Cocalia et al. (2006) which reported a high absorption efficiency of heavy metal ions when hydrophobic anions were used. Hydrophobic anions repel water molecules thus creating an environment conducive for IL-metal-ion complex formation.

Comparison of absorption vs. surface area (BET results)

After determining the absorption efficiencies of the polymers, it was necessary to assess whether there was any correlation between the amount of pollutant absorbed and the surface area of the polymers. The surface analysis data (Table 2) do not reveal any direct relationship between the amount of pollutant absorbed and the surface areas of the polymers. For example, both β-CDMIMOTs/HDI and β-CDPYROTs/HDI polymers showed 100% absorption efficiency for PNP, yet their surface areas were significantly different (23.26 m2·g-1 and 2.89 m2·g-1, respectively).

Scanning electron microscopy (SEM)

Scanning electron microscopy was carried out to determine the surface morphology of the polymers. This was done in order to determine whether the absorption efficiency of the polymers could be linked to the surface morphology of the polymers. The morphology of the polymers was found to have no bearing on the amount of the pollutant absorbed by the polymers. Although the polymers had different morphological appearances (see Fig. 3), their absorption efficiencies were still comparable. For example, although β-CDMIMOTs/TDI and β-CDMIMOTs/HDI appear different under a scanning electron microscope, they both absorbed 100% of Cr6+. However, the same polymers show different absorption capabilities for PNP. β-CDMIMOTs/TDI absorbed 77% of the model pollutant while β-CDMIMOTs/HDI exhibited an absorption efficiency of 80%.

 

 

Conclusion

Paranitrophenol, 2,4,6-trichlorophenol and Cr6+ were successfully extracted from an aqueous mixture using CD-IL. A high percentage removal by these ionic liquid polymers was observed after passing water containing the model pollutants through the polymers.. The polymers showed fairly high absorption efficiencies for both the inorganic (Cr6+) and organic pollutants (PNP and TCP). CD-IL polymers can potentially be used for the removal of both organic and inorganic pollutants from drinking water systems.

 

Acknowledgements

Financial assistance from the University of Johannesburg and the National Research Foundation (NRF) is appreciated.

 

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Received 16 May 2009; accepted in revised form 10 August 2009.

 

 

* To whom all correspondence should be addressed.
+2711 559-6516; fax: +2711 559-6425;
e-mail: bmamba@uj.ac.za