Metallurgical Industry

Determination of Palladium Content in Pd/C

1 Sample solution preparation
0.1g sample (precision to 0.0001g) was weighed and placed in a 250mL beaker, 15mL aqua regia (HCl: HNO3=3:1) was added, heated on hot plate.  After digestion, it was transferred to a 100mL volumetric flask, rinsed and made up to the volume with deionized water, shaken well.  Then 0.25mL sample solution was pipetted into a 100mL volumetric flask, then diluted and made up to the volume with deionized water, shaken well and spared for later use.

2 Experimental equipment and reagents 
AA7000 series atomic absorption spectrophotometer (with Pd hollow cathode lamp, EWAI Inc.)
Temperature-controlled hot plate
Nitric acid (HNO3): excellent grade purity
Hydrochloric acid (HCl): excellent grade purity
Palladium 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
Pd 244.8 0.2 10 1.5 2.0 Air - acetylene

4 Standard solution preparation
 Element   Concentration(μg/mL)
Pd 0 0.5 1.0 1.5 2.0

5 Standard curve
\
Pd Curve equation:y=0.0646*x-0.0002
Linearity coefficient:0.99969
 

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