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Aluminum Detection Using Eriochrome Cyanine R

Analytical method
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0% found this document useful (0 votes)
66 views4 pages

Aluminum Detection Using Eriochrome Cyanine R

Analytical method
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

Determination of Aluminum

“Eriochrome cyanine R: § dye method”

Principle:
Diluted solutions of Aluminum produce a red to pink complex with Eriochrome
cyanine R , which exhibits an absorption at 535 nm.

Eriochrome cyanine R
forms a blue color in
Complex formation with Al
Since a maximum absorption
Takes place at 535 nm

**The intensity of developed color influenced by:


1) Aluminum concentration
2) Reaction time
3) Temperature.
4) PH.
5) Alkalinity.
6) Concentration of other ions.
Reagents:
1) Stock Aluminum solution:
using KAl(SO4)2.12H2O as a source of Aluminum ion
3+
Prepare 500 mg/l Al as the following:
M wt of KAl (SO4)2.12H2O =39.7+27+2*96+ 12*18= 474.7

since 474 g of KAl (SO4)2.12H2O 27 g of Al

X -----------à 0.5 g Al
X = 0.5*474.7 /27 =8.791 g

Dissolve 8.791 g of KAl (SO4)2.12H2O in little amount of distillated water


and complete to 1 liter.
2) Eriochrome cyanine R: § dye
Preparation: Dissolve 150 mg in 50 ml distillated water
Add about 2 ml 1:1 acetic acid to adjust PH to 2.9
Complete to 100 ml with distillated water.
This dye solution stable for one year.
Function : uses for preparation working dye.
3) Working dye.
Preparation: Take 10 ml of dye stock and complete to 100 ml distillated water.
Stable for about 6 monthes.
Function: forms a blue color complex with Al3+ ion in acidic medium ,the color
intensity increase directly with concentration of Al3+ ion.
4) Buffer reagent:
Preparation: Dissolve 136 g sodium acetate in water + 40 ml 1N acetic acid
Then complete to 1 L.
Function: to adjust PH to 2.9 in which dye works.
5) Ascorbic acid:
Preparation: Dissolve 0.1 g of acid in 100 ml distillated water.
Function: prevents the interference of Fe , Mn ions thats commonly associate
the occurrence of Al3+ ions.
6) EDTA 0.01 M:
Preparation: Dissolve 3.7 g in 1 L distillated water.
Function: to remove any effective ion such as Fe , Mn, Al3+ ion from blank
sample
7) Sulfuric acid 0.02 N.
Function: to acidify the sample to the required PH.

Procedure:
1) Prepare a series of standers of Al3+ (from 0.01 mg/l to 0.3 mg/l) each
standard about 25 ml
We can use the standards 0.01, 0.05 , 0.1,15 , 0.2, 0.25 and 0.3 mg//l
The stock of Al3+ is 500 mg/l

Dilution low c1*v1=c2*v2


C1=500 mg/l
C2=0.01 mg/l
V2 =25 ml
500*v1= 0.01*25
V1=0.0005 ml
It's so far difficult to take this volume, so we can prepare an intermediate (100
ml) 5 mg/l standard as the following:
C1*v1=c2*v2
500*v1=5*100
V1=1 ml
Take 1 ml from the stock in 100 ml distillated water
Now let us prepare 25 ml 0.01 mg/l standard :

C1*v1=c2*v2
5*v1=0.01*25
V1= 0.05 ml
Also its difficult to take this volume so we will prepare an other intermediate (100 ml)
0.5 mg/l standard as the following:

C1*v1=c2*v2
5*v1=100*0.5
V1=10 ml.
Take 10 ml from 5 mg/l standard in 100 ml distillated water .

Now we sure that can prepare 25 ml 0.01 mg/l standard


C1*v1=c2*v2
0.5*v1=0.01*25
V1=1 ml
Take 1 ml from the last 0.5 mg/l standard in 25 ml distillated water .

Put your data in a table such as this

series concentration The ml taken in 25 ml The used intermediate standard


Total volume
1 0.01 1 0.5 mg/l
2 0.05 2.5
3 0.1 5
4 0.15 7.5
5 0.2 10
6 0.25 12.5
7 0.3 15

Note1 : there is no any a problem if you preferred to use the intermediate standard 5
mg/l beginning from 0.1 mg/l standard to the end of the series.

Note 2: this way of preparation of standards is selective, if you prefer other method
You can use it.
2) Add excess 1 ml sulfuric acid 0.02 N to standard sample or after the removing or
exceeding the alkalinity of the water sample.
3)add 1 ml ascorbic acid , 10 ml buffer reagent ,5 ml working dye and complete to 50
ml with distillated water
4)shake will and wait for 5-10 minutes.
5)the blank sample use either distillated water or 25 ml from the sample and add to
it 1 ml EDTA 0.01 M and then also do to it the steps from 2 -4.
6) Adjust the spectrophotometer on 535 nm since a maximum absorption at this
wavelength
7) Read the absorptions and draw a plot of the concentration against absorption

Written by Abu Alhassan Abd Alshafi


aboalhassan20082000@[Link]

aboalhassan20082000@[Link]

abo_alhassan2010@[Link]

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