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Quantitative Analysis of Iron Ion solution by UV-vis absorption Spectroscopy

Launch:2024-03-26    

I. The principle of quantitative analysis of UV-vis spectrum

    The UV-visible absorption spectrum is caused by the transition of valence electrons after the molecules (or ions) absorb ultraviolet or visible light (usually 200-800nm). Because the energy level transition between electrons is always accompanied by the transition between vibrational and rotational energy levels, the UV-vis spectrum shows a wide band .

   The absorption spectrum reflects the absorption ability of molecules to different wavelengths of ultraviolet light. If an organic compound is irradiated with a beam of ultraviolet light with continuous wavelengths, some wavelengths of ultraviolet radiation can be absorbed by the molecules of the compound. If the absorbance of different wavelengths is recorded, the ultraviolet absorption spectrum of the compound can be obtained. Lambert-Beer's law is the basic law of light absorption, commonly known as the law of light absorption. Under certain conditions, the maximum absorption wavelength of the reference material can be obtained by measuring the absorption peak of the reference material and its corresponding wavelength. Then in the selected wavelength range (or the maximum wavelength), taking the concentration and absorbance of the standard solution as Abscissa and ordinate, the standard curve of the composite solution is drawn, and the corresponding mathematical equation is obtained. The content of the compound in the solution to be tested was calculated according to the standard curve equation.

Lambert-Beer's law:A=lg(I0/It)=εbc

A: Absorbance, describing the degree of light absorption of the solution.

B: Liquid layer thickness (optical path length), usually in cm:

C: The molar concentration of the solution, in mol/L.

ε: Molar absorptivity: unit mol ·L-1 cm-1; is numerically equal to the absorbance of the solution at a certain wavelength when the concentration is 1mol/L and the thickness of the liquid layer is 1cm.

2. Experimental samples

Verification standard solution: iron (44.8mg/L).

Reagents: reagent A, reagent B

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Fig. 1 sample diagram

1-0.448mg/L Fe+0.5ml reagent An and 0.5ml reagent B.

2-0.896mg/L Fe+0.5ml reagent An and 0.5ml reagent B.

3-2.688mg/L Fe+0.5ml reagent An and 0.5ml reagent B.

4-4.480mg/L Fe+0.5ml reagent An and 0.5ml reagent B.

5-5.376mg/L Fe+0.5ml reagent An and 0.5ml reagent B.

III. Experimental equipment

In the experiment, the samples are tested, and the equipment used is as follows:

Spectrometer MS11639-E40090093 (200-1100nm).

Light sources: HL10000-mini-D51010172.

Optical fiber: QP100-0.2-SRR-SS.

Sampling accessories: three-way liquid spectrum measuring cell, quartz colorimetric dish.

IV. Experimental methods

    The light source is connected to one end of the liquid measuring cell through the optical fiber, the spectrometer is connected to the other end of the liquid measuring cell through the optical fiber, the spectrometer and the light source are plugged into the corresponding power adapter, and the data cable is connected to the computer.

    The UV-vis spectrum collection process of the sample is shown in the following figure:

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Figure 2. Equipment construction diagram


Iron: blank zero, take 10ml sample, add 0.5ml reagent An and 0.5ml reagent B, shake well, color for 5 minutes, collect absorption spectrum and record reading.

V. result analysis

The collection map is as follows:

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Fig. 3. UV-vis spectrum


Select the characteristic peak of 516nm, select the concentration range that the absorbance increases with the increase of concentration, and draw the iron ion concentration-absorbance curve :

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Figure 4. Absorbance curve

    The linear segment fitting was selected to obtain the quantitative measurement concentration range of 0mg/L~4.480mg/L, and the linear equation of iron ion concentration-absorbance was yttrium 0.2259x0.0038pm R 2 ~ 0.9998.

image.png

Figure 5. Absorbance curve

VI. Experimental conclusion

    In this experiment, iron ion was quantitatively detected by UV-vis spectrum, and the standard curve of iron ion concentration-absorbance was obtained by selecting the characteristic peak of 516nm. The range of quantitative measurement concentration was obtained by linear segment fitting. The range of quantitative measurement concentration was 0 mg ·L ~ (3 +). The equation of the standard curve was: y=0.2259x+0.0038. The detection results showed that there was a linear relationship between iron ion concentration and absorbance, and the sample concentration could be measured by spectral quantitative analysis.

VII. Instrument recommendation

    The instruments used in this study are spectrometer MS2000 and continuous halogen tungsten lamp HL10000-Mini developed by Ruhai Photoelectricity Institute.

MS2000 refrigerated optical fiber spectrometer

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  MS2000 is an industrial-grade high-resolution micro-fiber spectrometer with compact equipment structure and configurable spectral range, high resolution, up to 0.07nm, low stray light, ~ 2 ‰, and small temperature drift. it is suitable for many industrial field measurements, such as laser measurement, plasma emission spectrum measurement, color measurement, absorbance measurement and Raman measurement. It is an industrial grade optical fiber spectrometer with high performance and price.

Product model

MS2000

Optical parameters

Optical fiber interface

Key-SMA905

Number of pixel channels

2048

Stray light

~2‰

Wavelength temperature bleaching

~0.1pixel/

Consistency of optical fiber insertion and removal

≦7%

Functional parameters

AD sampling

16 bit

Data interface

USB2.0RS232

Extended function interface

24PIN

Acquisition mode

Single, continuous, software trigger, synchronous external trigger, asynchronous reset external trigger

Detector integration time

50 μs-65 s

CCD read noise1*

≦30

CCD dynamic range2*

35001

Signal-to-noise ratio

3801

Response linearity3*

98%

Weight

630 g

Dimension

125×95×35 mm

Operating temperature

0~40

Working humidity

 

20%-85%

*1Integration time 10ms, root mean square of CCD readout noise

*2The CCD dynamic range is 2ms when the integration time is the saturation value/the root mean square of the CCD readout noise

*3Response nonlinearity is before calibration