Catalyst and catalytic effect - 國立臺灣大學
Transcript of Catalyst and catalytic effect - 國立臺灣大學
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Catalyst and Catalytic Effect
Collect
◼ Plastic basin
◼ Watch glass
◼ 50 mL graduated cylinders (2)
◼ Plastic droppers (2)
◼ Cotton gloves
◼ Timer (by TA)
Prepare
◼ Test tubes (wash and dip dry)
◼ Test tube rack
◼ Tweezers
◼ 50 mL graduated cylinder
◼ 100 mL beaker
Share
◼ Knife and scissors
◼ Evaporating dish
◼ carton box
◼ Spray
◼ Incense and match (in hood)
2021/03/02 revised
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Objective
◼ Decomposition of hydrogen peroxide
◼ Chemiluminescence of luminol
◼ Catalytic effect of catalyst
Techniques
◼ Weighing
◼ Magnetic stirrer and hot plate
◼ Graduated cylinder and dispenser
◼ Liquid nitrogen
Objective & Techniques
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I. Decomposition of Hydrogen Peroxide
2 H2O2(aq) Catalyst O2(g) + 2 H2O(l)
發光胺
NH2 O
O
NH
NH+ 2OH- + 2H2O2
Iron ions+ 4H2O + N2
基態
hν
O-
O-
O
ONH2
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II. Chemiluminescence of Luminol
*
Luminol
Ground state
Catalytic Effect of Catalyst
▪ Catalyst
A catalyst is a substance
which increases the rate of
a chemical reaction
▪ Types
– Homogeneous catalyst
– Heterogeneous catalyst
– Biocatalyst (enzyme)
▪ Mechanism?
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Enzyme
◼ Enzyme: a biocatalyst
◼ Characteristics
– High specificity
– High efficiency
– Activity affected by pH, temperature… etc.
▪ Why?
▪ Protein: a polymer of amino acids
▪ Possess specific function for special structure
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Experimental Flowchart
I. Decomposition of H2O2
by catalyst
– MnO2(s)
– KI(aq)
– Pig liver
• Fresh
• Frozen
• Boiled
– Blood from pig liver
II. H2O2 and luminol
– Pig liver blood
– K3[Fe(CN)6]
– K4[Fe(CN)6]
III. Forensic chemistry
– Detection of blood
Step I. MnO2 and H2O2
• Weigh 0.1 g MnO2
and add 3 d
dishwashing liquid
into 50 mL graduated
cylinder
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• Add 5 mL H2O2 soln
• Mix well
• Record rxn time and
volume of bubbles
formed
• Insert burning
incense into gas
bubbles
• Inspect the property
of gas evolved
Step II. KI Solution and H2O2
Add 1 mL 2.0 M KI(aq)
and 3 d dishwashing liquid
To 50 mL graduated cylinder
Add 5 mL 10 mL 2%H2O2
Mix well
Record rxn time and volume
Test with burning incense 9
▪ Take 3 pieces of 50 mL graduated
cylinder
▪ Add 3 d dishwashing liquid and
1) Fresh pig liver
2) Frozen pig liver
3) Boiled pig liver
4) Blood from pig liver
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Record:
Rxn time &
bubble volumes
Cut to slices Freeze pig liver in liquid
nitrogen
5 mL of 3%H2O2
Step III. Pig Liver and H2O2
Step IV. Luminol and H2O2
Take 5 test tubes, each filled with
(1) 1 mL H2O & 2 d. blood from pig liver
(2) 1 mL 0.2 M K3Fe(CN) 6
(3) 1 mL 0.2 M K4Fe(CN)6
(4) 1 mL H2O & 1 d. K3Fe(CN) 6
(5) 1 mL H2O & 5 d. K3Fe(CN) 6
Use a test tube to take 3 mL luminol test
soln
Add 0.5 mL of luminol test soln to #(1)~(5)
one by one
Observe and record chemiluminescence
Add more Fe(III) to tubes (4) and (5)11
Step V. Luminol and Forensic
Collect the luminol test
soln left in a spray
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Spray the luminol test soln
on to tissue, knife, or
scissors used
Take the picture for
recording
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Summary I
3 d
dishwashing
liquid
+
5 mL
3%H2O2
Catalyst
0.1 g MnO2(s)
1 mL KI(aq)
Fresh pig liver
Frozen pig liver
Boiled pig liver
2 d Blood from pig liver
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Summary II
Test tube Reagent
1 mL H2O2 + 2 d. pig liver blood
0.5 mL
Luminol
test soln
1 mL 0.2 M K3Fe(CN) 6 +
1 mL 0.2 M K4Fe(CN)6
1 mL H2O & 1 d. K3Fe(CN) 6
1 mL H2O & 5 d. K3Fe(CN) 6
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Notice
◼ Start counting time while H2O2(aq) being added to
the reacting solution
◼ Take and place burning incense back into fume
hood to avoid smoke accumulating in lab.
◼ Wear cotton gloves to avoid burned by hot plate or
boiling water
◼ Be cautious of operating with liquid nitrogen for low
temperture
◼ Recycle the plastic droppers after used
◼ Boil all the pig liver after use and recycle
◼ Give the timer back to TA
◼ Clean the apparatus, lab bench after class
Brief report
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Dispenser
1. Check the pre-set volume and
do not change the volume
setting afterwards.
2. Position the flask under the tip
of dispenser.
3. Lightly pull the piston pump up
and down several times to get
rid of the bubbles.
4. Lightly pull piston pump up to
the top, then slowly push down
to obtain the measured solution.
(2)
(1)
(3)
(4)