International Journal of Polymer Science
Volume 2019 (2019), Article ID 4951327, 5 pages
https://doi.org/10.1155/2019/4951327

Research Article

Polymeric Composite Materials for the Detection of Barium Ions in Aqueous Solutions

Sergei Yu. Zaitsev, Marina S. Tsarkova, and Ilia S. Zaitsev

Federal State Budgetary Educational Institution of Higher Education, “Moscow State Academy of Veterinary Medicine and Biotechnology-MVA Named after K.I. Skryabin”, Moscow, Russia

Correspondence should be addressed to Sergei Yu. Zaitsev; s.y.zaitsev@mail.ru

Received 30 June 2018; Revised 4 December 2018; Accepted 27 December 2018; Published 3 February 2019

Academic Editor: Andrea Camposeo

Copyright © 2019 Sergei Yu. Zaitsev et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

The design of polymeric composite materials (PCM) for the optical control of chemical substances is currently one of the actively developing fields of science “at the junction” of polymer, organic, and analytical chemistry. The purpose of this work is the preparation of PCM containing derivatives of crown ethers for the optical determination of barium ions. The polymeric composite materials containing a novel optical molecular sensor have been obtained and investigated on the basis of a number of film-forming polymers. The best results have been obtained for PCM based on polyvinyl butyral films (since the fluorescence and absorption maxima shifted by 9 and 16 nm, respectively) in the fluorescence and absorption spectra of this PCM in the presence of barium ions. This makes the proposed PCM highly promising as sensor elements for the detection of the barium ions in the aqueous solutions.

1. Introduction

The design of polymeric composite materials (PCM) for the optical control of chemical substances is currently one of the actively developing fields of science “at the junction” of polymer, organic, and analytical chemistry [1–3]. One of the widely used approaches for PCM design is the preparation of blend compositions based on a number of necessary components: chromophores and one or more polymers or copolymers depending on the specific applications [4–6]. In addition, the most promising way is to prepare the polymer films a structure of which provides a combination of specific properties [6–8]. There are different polymers discussed in various publications [9–11] which can be used for such film preparations: simple polyvinyl polymers, polyacrylates, polymethacrylates, silicones, cellulose derivatives, etc. The main requirements for film-forming polymers in the case of our systems are the following: high water solubility (before film preparation) and an optimal degree of swelling (after film preparation), reasonable drying time, an optimal ratio between film flexibility and stability, possibility to mix with the most common plasticizers, and an ability to establish smooth and thin layers. The films prepared must be formed on the optical surface (from which a reliable signal can be obtained) and must have reasonable barrier properties, easy cation penetration to the photosensitive component, wash and/or sweat resistance, etc.

As a photosensitive component in these polymer systems, styryl dyes containing crown-ether groups (which ensure selective binding to the substances to be determined) can be optical molecular sensors (OMS). Such PCM can be promising for the determination of some metal ions. Many of these compounds have been studied by our research team in close cooperation with the Photochemistry Center of the Russian Academy of Sciences [4, 5, 12–16].

An international group of researchers from the Institute of Radiopharmaceutical Cancer Research (Helmholtz-Zentrum Dresden-Rossendorf, Germany) [17] reported recently about the synthesis of the calix[4]crown-6 derivatives modified with either cyclic amide moieties to chelate the barium ions. They measured the stability constants of the complexes between these modified calix[4]crown-6 derivatives and barium ions using NMR and UV/Vis titration techniques [17]. The log values obtained were in the range of 4.1-5.0 [17]. The authors [17] found an optimal derivative for barium extraction from the aqueous solutions but did not consider these derivatives for the detection of the barium ions. The Egyptian researchers [18] used anionic dyestuff “Rose Bengal” for barium detection. They claimed developed “sensor for simple, rapid, low cost, and reliable analysis of barium(II) ions in lithophone pigment and in industrial wastewater samples” at level 2.5 mg/L [18] but did not prove it in the practical trials. There are some older works on these topics that have been summarized in our book [19].

It is well known that soluble barium salts are toxic, for example, barium carbonate which is a rat poison. It is important to determine it in aqueous solutions because it can “affect the nervous system, causing cardiac irregularities, tremors, weakness, etc.” [20–22].

The purpose of this work is the preparation of polymeric composite materials (which contain photosensitive derivatives of crown ethers) for the optical detection of barium ions.

2. Experimental Part

2.1. Materials

In order to obtain the PCM, a novel azacrown-containing dye OMS (Figure 1) was synthesized in the Photochemistry Center of the Russian Academy of Sciences (Moscow, Russia) by Gromov [4] with the following structure: the dye was obtained by condensation of 1,4-dimethylpyridinium iodide (compound 2) with the formyl N-methylbenzoase-18-crown-6-ether derivative (compound 3) in the presence of pyrrolidine. According to the 1H NMR spectroscopy data, dye 1 exists as an E-isomer, which follows from the value of the spin-spin interaction constant of the protons of the ethylene fragment .

Figure 1: Chemical structure of the azacrown-containing dye OMS [4].

A mixture of 45 mg (0.19 mmol) of 1,4-dimethylpyridinium iodide (compound 2), 2.80 mg (0.23 mmol) of the formyl derivative of N-methylbenzoase-18-crown-6-ether (compound 3), and 3.6 ml of abs. EtOH and 0.04 ml of pyrrolidine (Scheme 1) were heated in an oil bath at 80°C for 25 hours. The reaction mixture was evaporated in vacuum, extracted with hot benzene to remove unreacted compound 3. The residue was dried in air, and dark red crystals were received in the amount of 59 mg (54%). Melting temperature was 163-164°С. The data of the 1H-NMR spectrum (Bruker DRX500, DMSO-d6, 23°C) were the following: 2.90 (s, 3 H, MeN), 3.41 (t, 2 H, NCH2CH2O, ), 3.54 (m, 4 H, 2 CH 2 O), 3.55 (m, 4 H, 2 CH 2 O), 3.62 (m, 4H, 2 CH2O), 3.72 (t, 2 H, NCH2CH2O, ), 3.85 (m, 2H, CH2CH2OAr), 4.17 (m, 2H, CH2OAr), 4.20 (s, 3 H, MeN +), 6.86 (d, 1 H, H (17), ), 7.22 (dd, 1H, H (18), , ); 7.30 (broad s, 1 H, H (20)), 7.32 (d, 1 H, CH (b), ), 7.91 (d, 1 N, CH (b), ), 8.08 (d, 2H, H (3), H (5), ), and 8.75 (d, 2H, H (2), H (6), ). Found (%): C, 52.86; H, 6.03; N, 4.74. For C₂₅H₃₅IN₂O₅, it is calculated, %: C, 52.64; H, 6.18; N, 4.91.

Scheme 1: Synthesis route of the dye OMS: iodide 1-methyl-4 - [(E) -2- (16-methyl-2,3,5,6,8,9,11,12,15,16-decahydro-14H-1,4,7,10,13,16-benzopentaoxaazazocycloooctadecine-19-yl) -vinyl] pyridinium (compound 1) using 1,4-dimethylpyridinium iodide (compound 2), N-methylbenzoase-18-crown-6-ether (compound 3), etc. (synthesized in the Photochemistry Center of the Russian Academy of Sciences by. Gromov [4]).

For the PCM preparation, the following polymers (Aldrich, USA) were used: cellulose acetate hydrophthalate (CAHP), cellulose acetate butyrate (CAB), polyvinyl butyral (PVB), and polyvinyl chloride (PVC). A commercially available plasticizer (Aldrich, USA), dioctyl sebacic acid (DSA), was used in the mixtures with the abovementioned polymers.

The following solvents (Chimmed, Russia) such as chloroform, acetonitrile, dichloroethane, tetrahydrofuran were used. Barium perchlorate Ba(ClO₄)₂ (99% from Aldrich, USA) and bidistilled water were used for the preparation of the “analyte” solutions.

2.2. Methods

First, the suitable solvents were found for polymer solution preparations. The optimal conditions were the following: 4% polymer solution of CAB or CAHP in acetonitrile, PVB in dichloroethane, and PVC in tetrahydrofuran. Second, the appropriate amount of OMS solution in chloroform (in the case of PVB or PVC) or acetonitrile (in the case of PVB or PVC) was added to the abovementioned polymer solutions.

From the solutions prepared, thin films were deposited onto quartz substrates (to have the possibility to measure absorption and fluorescence spectrum). Quartz glasses were placed on a special horizontal table at an adjustable level. On the glass with a pipette, a polymer solution was spread dropwise over the entire glass area. The membrane was cast and dried for 24 hours at room temperature in solvent vapors. The thickness of the membranes calculated was about 10 μm. The content of OMS in the membrane was about 1% of the weight of the polymer.

Absorption and fluorescence spectra were obtained on a Hitachi 330 and Shimadzu RF 5000 using quartz glasses (for films) and quartz cuvettes (for solutions). In the film and solution, in the presence of OMS, a marked peak was observed, the maximum of which was observed at the corresponding wavelength.

Then the films containing OMS were exposed to the aqueous solutions of salts for 10 minutes. Afterwards, the absorption and fluorescence spectra were recorded, and changes in the wavelength of the absorption or fluorescence maximum were noted. Statistical analysis was fulfilled using the standard packages of “STATISTICA 7” (StatSoft, USA) and “OriginPro 8” (OriginLab, USA).

3. Results and Discussion

First, the screening procedure for about 10 polymers (polyvinyl polymers, polyacrylates, polymethacrylates, cellulose derivatives, etc.) was carried out in order to find the most suitable compound for OMS immobilization.

The transparency of the polymer film before and after the OMS introduction (for the possibility of carrying out spectral studies) was the major criteria of the polymer selection. The following polymers were preliminarily investigated for the possibility of film formation: PVB, CAB, CAHP, PVC, polymethyl methacrylate (PMMA), copolymer of methylmethacrylate and ethyl acrylate (), polystyrene (PSt), copolymer of polystyrene and methyl acrylate (), copolymer of polystyrene and methyl methacrylate (), and polyvinylalcohol (PVA). All samples of PMMA and PSt films were very brittle, whereas PVA films, , , and copolymer films were turbid. Therefore, four types of polymers (PVB, CAB, CAHP, or PVC) were chosen that had a reasonable combination of all desirable properties. The novel OMS was completely and evenly (randomly) distributed in all these polymers as a structural matrix for PCM. After such preliminary experiments, the fluorescence spectra of OMS (Figure 2) introduced into the polymer matrices (based on PVB, CAB, CAHP, or PVC) were studied before and after the action of the analyte (solutions of barium perchlorates with the concentration of 10⁻⁶-10⁻³ mol/L).

Figure 2: Fluorescence spectra of OMS in the CAGF film before (dashed line) and after (solid line) incubation in the 10⁻³ M Ba(ClO₄)₂ solution.

The results of the relative changes of the fluorescence maxima in the spectra for various PCMs are presented in Table 1.

Table 1: The wavelength of the fluorescence maximum for PCM with OMS before and after incubation with Ba(ClO₄)₂.

Spectral characteristics
PVB
PVC
CAHP
CAB

λ₀ (before exposure), nm

λ₁ (after exposure), nm

Δλ, nm
+9
+3
+22
+1

Table 1 shows that the positions of the fluorescence maximum for OMS in polymer films are fairly close for PVB, PVC, and CAB (592-595 nm) and differ significantly from the λmax position for OMS in CAHP films (564 nm). This indicates the OMS and polymer interaction in the latter case. When the barium salt is applied to the polymeric films containing OMS, the absorption maximum shifts for all the PCM to the long-wavelength region of the spectrum. The largest shifts of λmax after adding barium perchlorate to solutions are observed for PCM based on PVB and CAHP.

It is assumed that OMS is presented in polymer films in the form of “head-to-tail” dimers formed during the electrostatic interaction of the crown-ether cycle and the pyridine part of the two closely packed OMS molecule. An interaction of OMS dimers with barium occurs ineffectively; a shift of 3 nm is observed in the case of PVC, which is a little bit higher than those in the case of a commercially available plasticizer (DSA) used without OMS. In the case of PVB, the shift is 9 nm which can be explained by the decay of some part of the OMS dimers due to their interaction with barium ions penetrating in the PVB matrix.

The interaction of CAHP carboxyl groups with charged pyridine part of the OMS molecule leads to the dissociation of the OMS dimeric form up to individual OMS molecules. Therefore, in the case of CAHP, the interaction of OMS with the barium ions is more efficient and accompanied by almost twofold increase in the fluorescence intensity (Figure 2). In this case, the shift of the maximum of fluorescence is the greatest (about 22 nm).

Then, the absorption spectra of OMS (Figure 3) introduced into a polymer matrix based on PVB, CAB, PVC, or CAHP were studied before and after the action of the “analytes” (solutions of barium perchlorate, with the concentration of 10⁻⁶ to 10⁻³ mol/L).

Figure 3: Absorbance spectra of OMS in the PVB film before (dashed line) and after (solid line) incubation in the 10⁻³ M Ba(ClO₄)₂.

The results of the absorption spectra for various PCMs are presented in Table 2.

Table 2: The wavelength of the absorbance maximum for PCM with OMS before and after incubation with Ba(ClO₄)₂.

Spectral characteristics
PVB
PVC
CAHP
CAB

λ₀ (before exposure), nm

λ₁ (after exposure), nm

Δλ, nm
+16
+3
+12
+3

Table 2 shows that for the PCM based on PVC and CAB, the shift in the absorption maximum is insignificant. The largest shifts of the absorption maximum are observed in the polymer films based on PVB (Figure 3) and CAHP. An important advantage of these films is the dependence of the magnitude of the absorbance maximum shift vs. Ba(ClO₄)₂ concentration (Table 3).

Table 3: Wavelength of the absorbance maximum for NCM with OMS in the PVB film at various concentrations Ba(ClO₄)₂.

Ва²⁺ concentration mol/L
λ₀, nm, (before impregnation)
λ₁, nm, (after impregnation)
Relative shift Δλ, nm

⁻³

+16

⁻⁴

+15

⁻⁵

+14

⁻⁶

+12

The large shifts observed in the absorption maximum and the dependence of the shift amount on the concentration of barium cations make the proposed composition as the most promising for the preparation of optical chemosensors for Ba²⁺ ions.

4. Conclusions

Thus, polymeric composite materials containing a novel optical molecular sensor have been obtained and investigated on the basis of a number of film-forming polymers. The best results have been obtained for PCM based on polyvinyl butyral films since the fluorescence and absorption maxima shifted by 9 and 16 nm, respectively (in the fluorescence and absorption spectra of this PCM by addition of barium ions). This makes the proposed PCM highly promising as materials for possible detection of the barium ions in aqueous solutions.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that there are no conflicts of interests regarding the publication of this paper.

Acknowledgments

The authors are thankful to Prof. S. P. Gromov and the coworkers in the Photochemistry Center of the Russian Academy of Sciences (Moscow, Russia) for providing OMS samples. This work was supported by the grant of the Russian Foundation for Basic Research (project number 18-016-00207).

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