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Determination of Maximum Wavelength
Determination of Maximum Wavelength
The spectrophotometer was used; the cell to be used for the UV/visible was washed thoroughly
with distilled water. Distilled water was used to calibrate the instrument at the wavelength of
400mm. therefore 0.001ml at the extract was diluted with 10ml of distilled water and 5ml of the
extract was measured and placed in the cell. The absorbance of the extract was determined
within the visible region (400-750nm) and the wavelength of maximum absorption ( γ max) of the
The melting point of the powdered flower was determined where small quantity of the powdered
flower was introduced into a capillary tube and the capillary tube is placed in melting point
The powder of the sun flower (Helicullum was dissolved in a beaker using methanol as a solvent
and 15ml of acetone and n-Hexane in ratio of 2:1 were mixed as the solvent mixture. Then the
dye was spotted unto the plate and allows it to run by capillary activities which the distanced
moved by the solvent is 8.0cm while the distance mixed by the solute (dye) is 0.8cm and the
retent factor was calculated by dividing the distance mixed by the solute over the distance mixed
by the solvent then finally the retention factor Rf of the sun flow was found to be 0.1
Ten (10) grams of the powder of sun flower was weighted using weigh balance and transferred
into a clean and dry beaker (250ml) size containing 50ml of methanol. The content was shaken
gently and the top was covered with aluminum foil and kept at room temperature for 24 hours (p
day) and filtered off using what man filter paper (cat no 1442 110) of pore size 110 mm. the
filtrated was concentrated by drying in a water bath until a brownish residue was allow to cooled
at room temperature for 1 hr before weigh the percentage yield at the calculated as:
weight of extract
Percentage yield= x 100
weight of sample
Determination of pH of Extract
10ml of extract was measured using measuring cylinder and transferred into a 50ml
standard volumetric flask. Distilled water was used to make the final volume. It was then
transfer into the sample bottle for pH analysis. The instrument used is multi-meter. HI
pH Measurement
The measurement was done simply successfully by submerged the tip of the probe into
The pH mode was pressed it was then stirred gently and waited to read and stabilized.
(0.1M NaOH and 0.1M HCl) for strong acid-strong base titration, (0.1M CH 3COOH and
0.1M NaOH) for weak acid strong base titration and finally (0.1M HCL and 0.1M Na 2CO3)
for strong acid weak base titration. The accuracy of the end point for the experimental
sample and trial was repeated three times to check the precision and reliability. The
titrations were again performed using phenolphthalein indicator as standard and the
results obtained were compared with the results of titrations using the flower extract
indicator. The end point of the titrations using the extract was reached when the colour
changed from yellow to colourless. The results of the titrations were shown in the table
2.
CHAPTER FOUR
4.1 RESULT
Parameters Values
Wavelength 450nm
pH 6.51
TABLE 2: Flower sample in different solvent (acidic and basic media) its color: