شماره ركورد كنفرانس :
3976
عنوان مقاله :
Optimization and simultaneous spectrophotometric determination of Thiosulfate and Sulfite in water samples based on insitu formation of AuNPs using PLSR
پديدآورندگان :
Saghi Salar Urmia University , Moghtader Mehdi Urmia University , Bahram Morteza m.bahram@urmia.ac.ir Urmia University
كليدواژه :
Sulfite , Thiosulfate , Experimental Design , AuNPs , PLSR
عنوان كنفرانس :
ششمين سمينار ملي دوسالانه كمومتريكس ايران
چكيده فارسي :
Sulfite and thiosulfate are two reducing agents which have been extensively used in
many industries for different purposes and as any other chemical pollutant in
environment, intake of excess amounts of them can cause severe health problems. So
various analytical methodologies have been employed for their determination in
environmental samples [1, 2]. AuNPs present interesting optical properties due to their
strong SPR absorptions in visible region of spectrum and their stability and ease of
preparation. An interesting application in this field is the employment of reducing nature
of analytes for insitu reduction of gold ions in solution and formation of AuNPs which
can be used as colorimetric sensors for analyte determination [3- 5]. On the other hand,
development of accurate and precise analytical methodologies for optimization and
simultaneous multicomponent determination in analyzed samples has an undeniable
importance which can be fulfilled by chemometrics especially in the case of
spectroscopic data which usually have a well-defined bilinear behavior. In the present
study, Partial Least Squares Regression has been used for simultaneous determination of
thiosulfate and sulfite in water samples based on the redox reaction of analytes with
Au(III) ions in the presence of SDS as surfactant and formation of AuNPs in solution
which exhibit SPR absorptions proportional to the analyte concentration. The effects of
various parameters on the formation of AuNPs including pH, time and concentrations of
Au(III) and SDS have been studied and optimized using a four factor Central Composite
Design. The spectra of samples were taken in ranges 400-800 nm with 1 nm intervals.
Analytical figures of merit have been investigated and Beer’s law obeyed over the
concentration range 4*10-5–1.6*10-4 mol. L-1. The accuracy of method has been
confirmed by recovery experiments.