An extractive spectrophotometric method for the determination of the trace amounts of tin has been carried out by employing 6-chloro-3-hydroxy-2-(2′-thienyl)-4-oxo-4H-1-benzopyran (in acetone) (CHTB) for the complexation of the metal ion in HCl medium. The colored species thus produced is quantitatively extracted into dichloromethane and shows the maximum absorbance at 432–437?nm. The method obeys Beer’s law in the range 0.0–1.3?μg?mL?1 of tin with molar absorptivity and Sandell’s sensitivity of ?L?mol?1?cm?1 and 0.0020?μg?Sn?cm?2, respectively, at 435?nm. The method is highly selective and free from the interference of a large number of elements including platinum metals. The ratio of metal to ligand in the extracted species is 1?:?2. Utilizing this method, the analysis of various synthetic and technical samples including gun metal and tin can have been carried out satisfactorily. 1. Introduction Tin does not occur free in nature and is found almost exclusively as tin oxide known as cassiterite or tin stone. Tin although a toxic metal, still it is being widely employed in manufacturing important alloys [1] and as solders for the joining of electronic components. The excess use of tin in daily life as fungicides in crops, in food packaging, and as stabilizer for polyvinyl chloride may introduce the inorganic tin {Sn(II) and Sn(IV)} in the environment. Out of these two, Sn(II) seems to be more toxic as compared to Sn(IV) [2]. In the literature, there are numerous analytical methods for the measurement of tin which are based on sophisticated instruments [3–10]. These methods are highly sensitive but generally tedious and prone to serious interferences from other elements. In contrast spectrophotometric methods are preferred due to their simplicity and speed in routine analysis. The reported studies have shown that a large number of reagents such as methyl orange [11], benzopyran derivatives [1, 12, 13], 2-(5-nitro-2-pyrilazo)-5-[N-n-propyl-N-(3-sulfopropyl)amino-phenoyl] [14], pyrocatechol violet [15–18], phenylfluorone [19, 20], dibromohydroxyphenylfluorone [21], arsenazo-M [22], isoamyl xanthate [23], diacetyl-monoxime-p-hydroxybenzoyl-hydrazine [24], bromopyrogallol red [25], potassium ethylxanthate [26], ferron [27], and 5,7-dichloro-8-quinolinol [28] have been used for the spectrophotometric determination of tin(II,IV) content. Among these many reagents [18, 21, 23, 26–28] are nonselective as they suffer from the interference, have low sensitivity [11, 12, 23, 24, 26–28], and some of them are time consuming, as they require time for full color
References
[1]
R. Kataria, H. K. Sharma, N. Agnihotri, and J. R. Mehta, “2-(2′-Furyl)-3-hydroxy-4-oxo-4H-1-benzopyran as a highly selective and sensitive reagent for spectrophotometric determination of tin(II),” Proceedings of the National Academy of Sciences of India, vol. 78, pp. 31–35, 2008.
[2]
T. Madrakian, A. Afkhami, R. Moein, and M. Bahram, “Simultaneous spectrophotometric determination of Sn(II) and Sn(IV) by mean centering of ratio kinetic profiles and partial least squares methods,” Talanta, vol. 72, no. 5, pp. 1847–1852, 2007.
[3]
C. Prior and G. S. Walker, “The use of the bismuth film electrode for the anodic stripping voltammetric determination of tin,” Electroanalysis, vol. 18, no. 8, pp. 823–829, 2006.
[4]
Y. Mino, “Determination of tin in canned foods by X-ray fluorescence spectrometry,” Journal of Health Science, vol. 52, no. 1, pp. 67–72, 2006.
[5]
J.-B. Liu and Y.-Z. Wu, “Rapid determination of tin in ore by atomic emission spectrometry,” Yejin Fenxi, vol. 33, no. 3, pp. 65–68, 2013.
[6]
Y. Lin, “Determination of tin in canned food with hydride-atomic fluorescence spectrometry,” Fenxi Ceshi Jishu Yu Yigi, vol. 19, pp. 149–152, 2013.
[7]
Y. Yu, Z.-Y. He, Z.-C. Mao et al., “Determination of tin in by spectral lines with different sensitivity of alternating current arc emission spectroscopy,” Yankuang Ceshi, vol. 32, pp. 44–47, 2013.
[8]
L. Pru?a, J. Dědina, and J. Kratzer, “Ultratrace determination of tin by hydride generation in-atomizer trapping atomic absorption spectrometry,” Analytica Chimica Acta, vol. 804, pp. 50–58, 2013.
[9]
S. V. de Azevedo, F. R. Moreira, and R. C. Campos, “Direct determination of tin in whole blood and urine by GF AAS,” Clinical Biochemistry, vol. 46, no. 1-2, pp. 123–127, 2013.
[10]
I. Trandafir, V. Nour, and M. E. Ionica, “Determination of tin in canned foods by inductively coupled plasma-mass spectrometry,” Polish Journal of Environmental Studies, vol. 21, no. 3, pp. 749–754, 2012.
[11]
X.-L. Wang, P. Zhang, and Y. Chen, “Spectrophotometric determination of stannum in copper alloy based on fading reaction of methyl orange,” Yejin Fenxi, vol. 32, no. 12, pp. 73–75, 2012.
[12]
R. Kataria and H. K. Sharma, “3-Hydroxy-2-[1′-phenyl-3′-(4″-methoxyphenyl) -4′-pyrazoyl]-4-oxo-4H-1-benzopyran as a spectrophotometric reagent for the micro-determination of tin,” Journal of the Indian Chemical Society, vol. 89, no. 1, pp. 121–126, 2012.
[13]
R. Kataria and H. K. Sharma, “An extractive spectrophotometric determination of tin as Sn(II)-6-chloro-3-hydroxy-7-methyl-2-(4′-methoxyphenyl)-4-oxo-4H-1-benzopyran complex into dichloromethane,” Eurasian Journal of Analytical Chemistry, vol. 6, no. 3, pp. 140–149, 2011.
[14]
B. Chen, Q. Zhang, H. Minami, M. Uto, and S. Inoue, “Spectrophotometric determination of tin in steels with 2-(5-nitro-2-pyridylazo)-5-[N-n-propyl-N-(3-sulfopropyl)amino]phenol,” Analytical Letters, vol. 33, no. 14, pp. 2951–2961, 2000.
[15]
J.-H. Tang, L.-H. Cheng, and X.-M. Wu, “Pyrocatechol violet-CPB spctrophotometric Determination of tin in copper alloys,” Guangpu Shiyanshi, vol. 30, pp. 1925–1928, 2013.
[16]
M. Abbasi-Tarighat, “Kinetic-spctrophotometric Determination of tin species using feed-forward neural network and radial basis function network in water and juices of canned fruits,” Analytical Chemistry, vol. 12, pp. 256–263, 2013.
[17]
T. Madrakian and F. Ghazizadeh, “Micelle-mediated extraction and determination of tin in soft drink and water samples,” Journal of the Brazilian Chemical Society, vol. 20, no. 8, pp. 1535–1540, 2009.
[18]
A. C. S. Costa, L. S. G. Teixeira, and S. L. C. Ferreira, “Spectrophotometric determination of tin in copper-based alloys using pyrocatechol violet,” Talanta, vol. 42, no. 12, pp. 1973–1978, 1995.
[19]
P. Huang, “Spectrophotometric determination of tin in antimony materials by using phenylflurone,” Hunan Youse Jinshu, vol. 29, pp. 68–79, 2013.
[20]
D.-X. Wang, F. Chen, and Z.-F. Liu, “Spectrophotometric determination of tin in flot glass,” The American Ceramic Society Bulletin, vol. 84, no. 12, pp. 9401–9404, 2005.
[21]
H. Yan, “Spectrophotometric determination of tin in steel with dibromo-hydroxyphenylfluorone,” Yejin Fenxi, vol. 23, no. 6, pp. 45–46, 2003.
[22]
C. Cai, Z. Zhou, S. Chen, and Y. Fang, “Research progress of tannery wastewater treatment,” Applied Mechanics and Materials, vol. 361–363, pp. 666–669, 2013.
[23]
S. P. Arya, S. C. Bhatia, A. Bansal, and M. Mahajan, “Isoamyl xanthate as a sensitive reagent for the spectrophotometric determination of tin,” Journal of the Indian Chemical Society, vol. 79, no. 4, pp. 359–360, 2002.
[24]
A. Varghese and A. M. A. Khadar, “Highly selective derivative spectrophotometric determination of tin (II) in alloy samples in the presence of cetylpyridinium chloride,” Acta Chimica Slovenica, vol. 53, no. 3, pp. 374–380, 2006.
[25]
X. Huang, W. Zhang, S. Han, and X. Wang, “Determination of tin in canned foods by UV/visible spectrophotometric technique using mixed surfactants,” Talanta, vol. 44, no. 5, pp. 817–822, 1997.
[26]
S. P. Arya and A. Bansal, “Rapid and selective method for the spectrophotometric determination of tin using potassium ethylxanthate,” Mikrochimica Acta, vol. 116, no. 1–3, pp. 63–71, 1994.
[27]
S. P. Arya, S. C. Bhatia, and A. Bansal, “Extractive-spectrophotometric determination of tin as Sn(II)-ferron complex,” Fresenius' Journal of Analytical Chemistry, vol. 345, no. 11, pp. 679–682, 1993.
[28]
A. M. Gutierrez, M. V. Laorden, A. Sanz-Medel, and J. L. Nieto, “Spectrophotometric determination of tin(IV) by extraction of the ternary tin/iodide/5,7-dichloro-8-quinolinol complex,” Analytica Chimica Acta, vol. 184, no. C, pp. 317–322, 1986.
[29]
G. H. Jeffery, J. Bassett, J. Mendham, and R. C. Denny, Vogels Textbook of Quantitative Chemical Analysis?Addison Wesley Longman, Singapore, 5th edition, 1989.
[30]
S. C. Gupta, N. S. Yadev, and S. N. Dhawan, “Synthesis of 2, 3 diaryl 8 methyl 2, 3, 4, 10 tetrahydropyrano 3, 2 b, 1 benzopyran 10 ones photoisomerization of styrylchromones,” Indian Journal Of Chemistry Section B: Organic Chemistry Including Medicinal Chemistry, vol. 30, no. 2, pp. 790–792, 1991.
[31]
A. Ringbom, “über die Genauigkeit der colorimetrischen Analysenmethoden I,” Fresenius Journal of Analytical Chemistry, vol. 115, no. 9–10, pp. 332–343, 1938.
[32]
P. Job, “Formation and stability of inorganic complexes in solution,” Annali di Chimica, vol. 9, pp. 113–203, 1928.
[33]
W. C. Vosburgh and G. R. Cooper, “Complex ions. I. The identification of complex ions in solution by spectrophoto-metric measurements,” The Journal of the American Chemical Society, vol. 63, no. 2, pp. 437–442, 1941.
[34]
J. H. Yoe and A. L. Jones, “Colorimetric determination of iron with disodium-1,2-dihydroxybenzene-3,5-disulfonate,” Industrial & Engineering Chemistry Analytical Edition, vol. 16, no. 2, pp. 111–115, 1944.