Metallurgical Industry

Determination of Sodium and Barium Content in Strontium Carbonate

1 Sample solution preparation
Approximately 0.4g sample (precision to 0.0001g) was weighed and placed in a 250mL beaker, 10mL deionized water was added, covered with surface dish.  2mL hydrochloric acid solution was added for digestion, boiled for 2min.  After cooling down, it was transferred into a 100mL volumetric flask.  1mL 38% KCl solution, 1mL of hydrochloric acid were added, diluted and made up to the volume with water, shaken well and set aside for later use.

2 Experimental equipment and reagents 
AA7000 series atomic absorption spectrophotometer (with Zn, Al hollow cathode lamp, EWAI Inc.)
Temperature-controlled hot plate
Hydrochloric acid (HCl): excellent grade purity
Potassium chloride (KCl): excellent grade purity
Sodium standard solution (National Reference Materials Research Center)
Barium standard solution (National Reference Materials Research Center)

3 Instrument conditions
Parameter Wavelength
(nm)
Slit width(nm) Burner height(mm) Fuel gas flow rate(L/min) Lamp current(mA) Flame type
Na 589.0 0.2 10 1.5 3.0 Air – acetylene
Ba 553.6 0.2 10 4.0 3.0 Air – acetylene

4 Standard solution preparation
 Element Concentration(μg/mL)
Na 0 0.2 0.4 0.8 1.6
Ba 0 5.0 10.0 15.0 25.0

5 Standard curve
\
Na Curve equation:y=0.43365*x+0.00834
Linearity coefficient:1.00000
\
Ba Curve equation:y=0.0030*x+0.0036
Linearity coefficient:0.99988
 
 

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