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. 2014 Feb 6;9(1):62. doi: 10.1186/1556-276X-9-62

Highly selective colorimetric detection and preconcentration of Bi(III) ions by dithizone complexes anchored onto mesoporous TiO2

Mohd Faisal 1, Adel A Ismail 1,2,✉, Farid A Harraz 1,2, Houcine Bouzid 1,4, Saleh A Al-Sayari 1,3, Ali Al-Hajry 1,4
PMCID: PMC3922967  PMID: 24502680

Abstract

We successfully developed a single-step detection and removal unit for Bi(III) ions based on dithizone (DZ) anchored on mesoporous TiO2 with rapid colorometric response and high selectivity for the first time. [(DZ)3-Bi] complex is easily separated and collected by mesoporous TiO2 as adsorbent and preconcentrator without any color change of the produced complex onto the surface of mesoporous TiO2 (TiO2-[(DZ)3-Bi]) at different Bi(III) concentrations. This is because highly potent mesoporous TiO2 architecture provides proficient channeling or movement of Bi(III) ions for efficient binding of metal ion, and the simultaneous excellent adsorbing nature of mesoporous TiO2 provides an extra plane for the removal of metal ions.

Keywords: Mesoporous TiO2, Optical sensor, Detection, Preconcentration, Bi(III) ions

Background

Bi(III) ion in the environment is highly fatal to human beings and in particular to aquatic species in seawater. The development of solely selective, separation, preconcentration, and detection method for Bi(III) ions at ultratraces is a challenging task because of their very low concentrations in natural samples and strong interference from the real sample matrices. Thus, in recent years, considerable attention has been focused on the preconcentration and/or monitoring of ultratrace Bi(III) ions [1]. Solid phase extraction techniques have provided excellent alternative approach to liquid-liquid extraction for Bi(III) preconcentration prior to analyte determination step [2-4]. Several supporters such as silica [5-7], clays [8], biomass [9], resins [10,11], and carbons [12,13] have been modified with chelating groups for the adsorption of heavy metal ions. In our previous work, first molecular receptors were anchored onto mesoporous silica and then this framework was used for the detection of metal ions [14-21]. However, few reports are available for the detection of heavy metals using TiO2 films [22,23]. Nanocrystalline TiO2 films were employed for naked-eye colorimetric detection of mercury in aqueous solution using N719 dye (N719 = bis(2,2A-bipyridyl-4,4A-dicarboxylato) ruthenium(II) bis(tetrabutylammonium) bis(thiocyanate)) [22,23]. Mesoporous TiO2 is supposed to be a potentially active material for designing optical sensor due to its excellent surface area and high optical transparency in the visible part of the spectrum [22]. When mesoporous TiO2 is dispersed in water, then the surface becomes anionic in nature and increases in surface area that would render the more coverage of hydroxyl groups (OH) from H2O [24]. In sensing application, mesoporosity provides the desired high accessible surface and easier movement of metal ions for efficient binding; simultaneously excellent adsorbing properties of mesoporous TiO2 provide an extra plane for removal of metal ion. In this contribution, we successfully detect and preconcentrate Bi(III) ion in a single step using mesoporous TiO2 without any color change of the produced complex [(DZ)3-Bi] onto the surface of mesoporous TiO2 {TiO2-[(DZ)3-Bi]} at different Bi(III) concentrations. To the best of our knowledge, this is the first report briefing the single-step detection and removal of Bi(III) ions utilizing mesoporous TiO2.

Methods

Materials

The block copolymer surfactant EO106-PO70EO106(F-127,EO = -CH2CH2O–,PO = -CH2(CH3)CHO–), MW (12,600 g/mol), Ti(OC(CH3)3)4 (TBOT), HCl, CH3OH, C2H5OH, CH3COOH, and dithizone were purchased from Sigma-Aldrich (St. Louis, MO, USA).

Preparation of mesoporous TiO2

Mesoporous TiO2 nanocrystals were synthesized through a simple one-step sol–gel process in the presence of the F127 triblock copolymer as a structure-directing agent. To minimize possible variables, the molar ratio of each reagent in the starting solution was fixed at TiO2/F127/C2H5OH/HCl/CH3COOH = 1:0.02:50:2.25:3.75. In particular, 1.6 g of F127, 2.3 mL of CH3COOH, and 0.74 mL of HCl were dissolved in 30 ml of ethanol and then added to 3.5 ml of TBOT [25]. The mixture was stirred vigorously for 60 min and transferred into a Petri dish. Ethanol was subsequently evaporated at 40°C, and a relative humidity of 40% for 12 h was set followed by the transfer of the sample into a 65°C oven and ageing for an additional 24 h. The as-made mesostructured hybrids were calcined at 450°C in air for 4 h at a heating rate of 1°C/min and a cooling rate of 2°C/min to remove the surfactant and to obtain the mesostructured TiO2.

Characterization

Transmission electron microscopy (TEM) was conducted at 200 kV with a JEOL JEM-2100 F-UHR field-emission instrument (Tokyo, Japan) equipped with a Gatan GIF 2001 energy filter (Pleasanton, CA, USA) and a 1 K CCD camera in order to obtain EEL spectra. Field emission scanning electron microscope (FE-SEM) images were carried out with a FE scanning electron microanalyzer (JEOL-6300 F, 5 kV). X-ray diffraction (XRD) data were acquired on a PANalytical X’ port diffractometer using CuKα1/2, λα1 = 154.060-pm and λα2 = 154.439-pm radiation. Raman spectroscopy was carried out using a Perkin Elmer Raman Station 400 (Waltham, MA, USA). The nitrogen adsorption and desorption isotherms were measured at 77 K using a Quantachrome Autosorb 3B after the samples were vacuum-dried at 200°C overnight. The sorption data were analyzed using the Barrett-Joyner-Halenda (BJH) model with Halsey equation [26]. Fourier transform infrared spectroscopy (FTIR) spectra were recorded with a Bruker FRA 106 spectrometer (Ettlingen, Germany) using the standard KBr pellet method. Reflectance spectrum was taken at room temperature using UV-visible spectrophotometer (lambda 950 Perkin Elmer) fitted with universal reflectance accessory in the range of 200 to 800 nm and using BaSO4 as reference.

Bi(III) ion detection

The solutions of different concentrations of Bi(III) ions ranging from 0.001 to 1 ppm were prepared in a buffer solution of pH 4. The working solution of DZ was prepared by dissolving 10 mg of dithizone in 100 ml of ethanol. The buffer solution of 0.2 M KCl-HCl of pH 2, 0.1 M CH3COOH–CH3COONa of pH 4, sodium dihydrogen phosphate and disodium hydrogen phosphate solution of pH 7, and 0.1 M disodium hydrogen phosphate-HCl of pH 9 was used to study the effect of pH on the adsorption of the Bi(III) ions on the designed nanosensors. A series of experiments has been carried out for the different concentrations of Bi(III) ions ranging from 0.001 to 100 ppm. For the detection of the metal ions, 5 mg of mesoporous TiO2 was constantly stirred in 20 ml of metal-ion solution of desired pH for 5 min to achieve the heterogeneous solution. One milliliter ethanolic solution of DZ was added to the above solution at room temperature with constant stirring for 1 min. The solution was then filtered using Whatmann filter. The filtrate was then analyzed for metal ion and absorbance using UV-visible spectrophotometer (lambda 950 Perkin Elmer). Bi(III) sorption took place quantitatively as indicated from the analysis of the Bi(III) ions in effluent solutions by ICP-OES. After extraction, the ultratrace concentrations of the remained ions in the test aqueous solutions were estimated by ICP-MS. Also, the TiO2-DZ-Bi complex was analyzed by UV-visible diffuse reflectance spectra by collecting the material from Whatmann filter. Reflectance spectrum was taken at room temperature using UV-visible spectrophotometer (lambda 950 Perkin Elmer) fitted with universal reflectance accessory in the range of 200 to 800 nm.

Results and discussion

The prepared mesoporous TiO2, TiO2-DZ, and TiO2-[(DZ)3-Bi] have been investigated. XRD pattern reflections from anatase phases with peaks characteristic for the (101), (004), (200), (211), and (213) lattice planes evince that TiO2 phase easily nucleates during heating and subsequently transforms into nanocrystals upon calcination at 450°C (see Additional file 1: Figure S1). Even upon the addition of DZ anchored on the mesoporous TiO2 (Additional file 1: Figure S1, curve b) and after the (Bi(DZ)3) complex was collected onto the surface of mesoporous TiO2, the intensity of the mean peak (101) for all the samples was similar and there is no significant change in the crystallinity of the TiO2 anatase phases. Nitrogen adsorption isotherms of the TiO2 mesoporous and TiO2-DZ are investigated (see Additional file 2: Figure S2). Typical reversible type-IV adsorption isotherms are found for both samples. The sharpness of the inflection resulting from capillary condensation at relative pressures p/p0 between 0.45 and 0.7 is characteristic for mesostructures. The mesoporous TiO2 possesses high surface areas of 174 m2 g-1 and large pore volumes of 0.29 cm3 g-1 at 450°C; they are reduced to 143 m2 g-1 and 0.22 cm3 g-1, respectively, as a result of the DZ probe anchoring the pores. Also, the pore diameter is slightly decreased from 8.11 to 6.3 nm; this further confirms the DZ probe anchoring the pores.

For the first time, we have successfully designed a highly sensitive novel sensing system and preconcentrator based on mesoporous TiO2. Small particles and large surface area of mesoporous TiO2 play an important role in terms of accessibility and adsorption amount. These characteristic features of sensing system increase the possibility of binding events or complex formation between metal ions and sensor, as clearly shown by our results in which the TiO2/DZ-based nanosensor shows excellent sensing performance at ultratrace level of concentrations and also the simultaneous removal of Bi(III) ions (Figure 1). The mechanism based on binding of the Bi(III) ion with organic chromospheres (DZ) in the solution phase led to color change which corresponds to the formation of complex between Bi(III) ion and DZ, and the final interaction of the formed complex with mesoporous TiO2 led to the formation of stable TiO2-[(DZ)3-Bi] complex which can be easily separated by simple filtration, leaving behind clear transparent filtrate (Figure 1). The sensing system responds very fast regardless of Bi(III) concentration and demonstrates color change only in few seconds. Furthermore, the designed sensor completely removed the color complex without any leaching, leaving a colorless and transparent filtrate, suggesting the stable binding between the mesoporous TiO2 and [(DZ)3-Bi] complex and also the complete removal of Bi(III) ions (Figure 1).

Figure 1.

Figure 1

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Sensing mechanism based on binding 0.5-ppm solution of Bi(III) ion with organic chromospheres (DZ) in solution-phase. The binding led to color change which corresponds to the formation of complex between the Bi(III) ion and DZ, and the final interaction of the formed complex with the mesoporous TiO2 led to the formation of highly stable TiO2-[(DZ)3-Bi] complex.

The TEM images of the TiO2-DZ and TiO2-[(DZ)3-Bi] samples were investigated (Figure 2). It is clearly seen that all the particles are spherical in shape with a uniform size distribution. Interestingly, there is no change in the shape and uniformity of TiO2 after anchoring the DZ probe (TiO2-DZ) and even TiO2-[(DZ)3-Bi] complex (Figure 2a,b). The TEM images indicated that the prepared TiO2 was mesoporous in nature (Figure 2a,b). The particle size of the TiO2 nanocrystals has been measured to be appropriately 10 nm. As seen in the HRTEM images (Figure 2c,d), the atomic planes of the TiO2 particles are separated by 3.54 Å, which agrees with the (101). It is important to note that the incorporation of either DZ or [(DZ)3-Bi] complex into the TiO2 framework does not have an effect on the mesostructure. The selected area electron diffraction (SAED) pattern (Figure 2c,d inset) further confirms that the TiO2 anatase is formed. The EDS analysis showed that there is a representative EDS pattern of the TiO2-DZ (Figure 2e) and even TiO2-[(DZ)3-Bi] complex (Figure 2f), and it revealed the presence of Ti, O, and C elements in the obtained TiO2-DZ; however, the Ti, O, C, and Bi elements were detected in the TiO2-[(DZ)3-Bi] sample. This indicated that the DZ probe is anchored onto the TiO2 network, and in the case of TiO2-[(DZ)3-Bi], Bi is observed as well; this further confirms that the [(DZ)3-Bi] complex was formed into the TiO2 pores. The FTIR spectra for the meso-TiO2, TiO2-DZ, and TiO2-DZ-Bi samples revealed a broad absorbance peak in the range from 3,100 to 3,450 cm-1 assigned to hydroxyl vibration and a strong absorbance peak around 1,628 cm-1 attributed to the vibrations of the surface-adsorbed H2O and Ti-OH bonds (see Additional file 3: Figure S3). Also, after anchoring DZ, as you see in either TiO2-DZ or TiO2-[(DZ)3-Bi] samples, the FTIR spectra show distinct absorption peaks at 1,435 cm-1 corresponding to the C = S stretching mode, while the peak shifts to 1,352 cm-1 for the TiO2-[(DZ)3-Bi] sample due to the introduction of Bi(III) in C = S-Bi [27]. In the TiO2-DZ and TiO2-[(DZ)3-Bi] samples, the absorption peaks at 1,540 cm-1 is attributed to the benzene ring stretching band, whereas in the spectrum of TiO2-[(DZ)3-Bi], the peaks shift to 1,523 cm-1 due to the formation of Bi-N bond in Bi-N-C6H5.

Figure 2.

Figure 2

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TEM and HRTEM images and EDS analysis of the samples. TEM images of TiO2-DZ (a) and TiO2-[(DZ)3-Bi] (b) samples. HRTEM images of TiO2-DZ (c) and TiO2-[(DZ)3-Bi] (d). The EDS analysis of TiO2-DZ (e) and TiO2-[(DZ)3-Bi] complex (f).

For the detection of Bi(III) ions, 5 mg of mesoporous TiO2 was constantly stirred in 20 ml of Bi(III) ion solution at different concentrations and pH value of 4 for 5 min to achieve the heterogeneous solution. One milliliter ethanolic solution of DZ was added to the above solution at room temperature, and the mixture was left to allow reaction for 1 min. Change in color can be easily distinguished by naked eye, and optical changes can be easily quantified by UV-visible spectroscopy. Wide range of Bi(III) ion concentrations (0.001 to 1 ppm) has been studied using UV spectroscopy. The designed nanosensor shows high sensing ability at trace-level concentration of Bi(III) ion, suggesting easier flow of Bi(III) ion over a wide range of concentrations (Figure 3a). Mesoporous TiO2-based sensing system can be utilized in two ways, as a chemosensor simply by visual inspection and simultaneously this potentially interesting material could also serve as preconcentrators to provide high adsorption efficiency to remove the toxic metal ions in a single step by a strong interaction between the TiO2 and the [(DZ)3-Bi] complex. Our designed sensor provides a simultaneous detection and removal of Bi(III) ions without the use of sophisticated instrument. The stability of the DZ probe with TiO2 can be assessed by the fact that there was no indication of elution of the probe molecules during the detection of Bi(III) ion. Transparent, clear filtrate obtained after filtration confirmed the firm integration of mesoporous TiO2 and Bi(DZ)3 complex and also the preconcentrator properties of the designed sensing system. Besides that, the addition of Bi(III) ion which led to a rapid color transformation provides a very simple, sensitive and selective detecting approach. As can be seen from Figure 3a, in the absence of Bi(III) ions, the color of the designed sensor is light yellow or mud but after the formation of the [Bi(DZ)3] complex, the color becomes light orange (at 0.001 ppm of Bi), indicating the presence of Bi in the formed complex at very low concentration of the Bi(III) ions. As the concentration of the Bi(III) ions increases, the intensity of the color also increases and becomes brick color at high concentration of the Bi(III) ions. The rapid color changing behavior of the newly developed sensing system upon the addition of the Bi(III) ions may be due the fact that highly potent mesoporous TiO2 architecture provides proficient channeling or movement of the Bi(III) ions for efficient binding of metal ion, and the simultaneous excellent adsorbing nature of the mesoporous TiO2 provides an extra plane for the removal of metal ions. Figure 3b shows the spectral patterns obtained with DZ-based sensor in the absence (blank) and in the presence of 0.5 ppm Bi(III) ions. As can be seen, in the absence of the Bi(III) ions, i.e., blank which shows an absorbance maxima at 434 and 580 nm. The shorter wavelength corresponds to thiol, and the longer wavelength corresponds to the thione group of DZ. On the other hand, with 0.5-ppm Bi(III) ion solution, a complex formation occurs, and a single band appears near to 502 nm which confirms the formation of the [Bi(DZ)3] complex [18-21]. The absorbance at 502 nm was used to calculate the concentration of the [Bi(DZ)3] complex. Table 1 shows the absorbance value at 502 nm for each concentration studied.

Figure 3.

Figure 3

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Color changes and spectral patterns. (a) The sequence of concentration-dependent changes in color of TiO2-DZ nanosensor after the detection of Bi(III) ions at different concentrations. (b) Spectral patterns obtained with DZ in the absence (blank) and in the presence of 0.5 ppm Bi(III) ions after 1-min reaction time at pH 4.

Table 1.

Absorbance values at 502 nm for each concentration studied

No. Concentration of Bi(III) ions in ppm Absorbance (a.u.)
1
 0.001
 0.1735
2
 0.005
 0.1771
3
 0.01
 0.1842
4
 0.05
 0.188
5
 0.1
 0.1936
6
 0.5
 0.197
7 1.0 0.217
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One of the major advantages of the current proposed sensing system is the selective sensing performance in the presence of interfering cations and anions even at 5,000-times-more concentration of the interfering components in comparison to Bi(III) ions (see Additional file 4: Table S1). Thus, the current approach presents a highly selective nanosensor for the efficient recognition of Bi(III) ions. To study the interfering effect of possible cations and anions which may present with Bi(III) ions in the surrounding environment or wastewater, we added the interfering cations and anions to a 0.5-ppm solution of Bi(III) ions in the presence of the proposed nanosensor at pH 4. To ensure the selective performance of our TiO2-based sensor, we carried out the experiments up to high tolerance concentration of interfering cations and anions. The results show no significant changes at very high concentrations in color pattern obtained after the addition of various types of interfering cations and anions, confirming the highly selective nature of this mesoporous TiO2-based sensor. Only Fe+3, Cr+3, and Hg+ cations show interfering effect at high concentrations, i.e., 100 ppm or above out of the several cations taken into consideration. In case of anions only, I- shows slight color change at 250 ppm which is almost 5,000 times more than the Bi(III) ion concentration.

Conclusions

In summary, a very simple sensing approach for one-step detection and collection of Bi(III) ions without the use of any sophisticated technique or further modification of mesoporous TiO2-based nanosensor is demonstrated, and the sensing results could be easily detected by naked eye. The detection limit for the Bi(III) ions using mesoporous TiO2-based sensor is estimated to be approximately 1 ppb. The results presented herein have important implications in the development of colorimetric sensors based on mesoporous TiO2 nanocrystals for the simple, swift, and selective detection of toxic metal ions in solution.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

All authors participated in the design of the study. MF, AI, and FH carried out all the experiments. HB measured and analyzed the data of TEM and XRD. MF, AI, and FH participated in analysis of the results and drafted the manuscript. All authors, especially SAS and AAH, provided comments/suggestions to revise it. All authors read and approved the final manuscript.

Supplementary Material

Additional file 1

XRD patterns of the samples.

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Additional file 2

N 2 sorption isotherms and pore size distributions (inset) of the of the samples.

Click here for file (84.5KB, doc)
Additional file 3

FTIR spectra for all the samples.

Click here for file (183.5KB, doc)
Additional file 4

Contains a table that summarizes the color trend obtained for various interfering cations and anions.

Click here for file (49.5KB, doc)

Contributor Information

Mohd Faisal, Email: mdfaisalahsan@gmail.com.

Adel A Ismail, Email: adelali141@yahoo.com.

Farid A Harraz, Email: fharraz68@yahoo.com.

Houcine Bouzid, Email: houcinebouzid@yahoo.fr.

Saleh A Al-Sayari, Email: salehalsayari@gmail.com.

Ali Al-Hajry, Email: ahajry@gmail.com.

Acknowledgements

The authors would like to acknowledge the support of the Ministry of Higher Education, Kingdom of Saudi Arabia for this research through a grant (PCSED-017-12) under the Promising Centre for Sensors and Electronic Devices (PCSED) at Najran University, Kingdom of Saudi Arabia.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Additional file 1

XRD patterns of the samples.

Click here for file (208.5KB, doc)
Additional file 2

N 2 sorption isotherms and pore size distributions (inset) of the of the samples.

Click here for file (84.5KB, doc)
Additional file 3

FTIR spectra for all the samples.

Click here for file (183.5KB, doc)
Additional file 4

Contains a table that summarizes the color trend obtained for various interfering cations and anions.

Click here for file (49.5KB, doc)

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