Catalysts for the thermal decomposition of potassium chlorate

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Apparatus and chemicals

Face shield

Each demonstration requires:

Pyrex test-tubes (150 mm x 15 mm), 3 (One for each catalyst to be shown plus one for the control) (see note 1)
Bunsen burner
Retort stand with boss and clamp
Filter funnel
Conical flask (1 dm³) to collect filtrate
Watch glass, a little larger than the filter paper
Stopwatch or stopclock

Access to:
Top pan balance (2 dp)
Oven
Wash bottle of deionised water
Filter paper (e.g. Whatman no.1)
Wooden splints
Mineral wool (optional)

Potassium chlorate(V), KCIO₃ (Oxidising, Harmful), 5 g. This is enough to demonstrate one catalyst plus a control. A further 2.5 g is needed for each additional catalyst.
Sodium chlorate(V), NaCIO₃ (Oxidising, Harmful) can be used instead of potassium chlorate(V).

You need 0.25 g of each catalyst. Suitable catalysts include copper(II) oxide, CuO (Harmful); manganese dioxide, MnO₂ (Harmful); iron(III) oxide (ferric oxide), Fe₂O₃; silicon dioxide (silica gel), SiO₂. See note 2.

Technical notes

Potassium chlorate(V) (Oxidising, Harmful) Refer to CLEAPSS Hazcard 77
Sodium chlorate(V) (Oxidising, Harmful) Refer to CLEAPSS Hazcard 77
Copper(II) oxide (Harmful) Refer to CLEAPSS Hazcard 26
Manganese dioxide (Harmful) Refer to CLEAPSS Hazcard 60

1 Make sure the test-tubes are scrupulously clean as potassium (or sodium) chlorate(V) reacts violently with any oxidisable material. Weigh 2.5 g of potassium chlorate(V) into each of the test-tubes. Weigh 0.25 g of copper(II) oxide into the test-tube for the catalyst experiment. Mix carefully (do not grind the mixtures of potassium chlorate to provide a greater surface area, there is a danger of explosion). If further catalysts are used then add 0.25 g of each to the designated test-tube for that catalyst.

2 Take great care not to use carbon (charcoal) in place of the catalyst: serious accidents have resulted.

Effects of catalysts on the decomposition of potassium chlorate

Procedure

HEALTH & SAFETY: The teacher carrying out the demonstration must wear a full face shield

a Set up the apparatus behind safety screens. Clamp the test-tube at about 45° with its base about 5 cm above the Bunsen burner. It is best to do a preliminary experiment to find a suitable distance between the Bunsen and the bottom of the test-tube. Mark the positions of the clamp and the Bunsen so that it is easy to replace them in the same positions.

b Light the Bunsen, turn the gas fully on and open the air hole, at the same time start the stopwatch. The solid melts and begins to decompose, giving off bubbles of oxygen. Hold a glowing splint at the mouth of the test-tube. When it relights, stop the clock and note the time taken for the splint to relight. Turn off the Bunsen.

c Clamp the test-tube with potassium chlorate and copper(II) oxide catalyst in the same place as before. Light the Bunsen as before. Start heating, start the stopwatch. Hold a glowing splint at the mouth of the test-tube and note the time it takes to relight. This should be between a quarter to one third of the time taken for the original.

d Repeat for any other catalysts if you wish to show further experiments and compare the effectiveness of catalysts.

e Because potassium chlorate(V) is such a powerful oxidising agent you must be careful not to drop the glowing splint into the molten liquid. A loose plug of mineral wool near the mouth of the test-tube prevents this.

Catalyst recovery (optional)

a Weigh one of the filter papers after they have been dried in the oven.

b Allow the test-tube containing the potassium chlorate and copper oxide to cool. Add a little distilled water to the test-tube and warm gently to dissolve the potassium chlorate.

c When it has dissolved, filter the contents of the test-tube through the pre-weighed filter paper, using a wash bottle and distilled water to ensure that all the contents are transferred.

d Wash the residue on the filter paper two or three times with distilled water to remove any potassium chlorate. Place the filter paper on a watch glass in an oven to dry.

e When dry (this may need to be the following lesson), re-weigh the filter paper and dry catalyst. With care and good technique, the weight of the recovered catalyst is within a few per cent of the initial amount used. This can be tricky as students are often not prepared to accept any loss and the value of the lesson can be diminished.

Teaching notes

Recovering the catalyst is most obvious with the black catalysts, copper(II) oxide and manganese dioxide.

There are opportunities to discuss the factors that must be controlled to make the experiment a ‘fair test’.

You may prefer not to do the catalyst recovery part of the demonstration, leaving it as a ‘thought experiment’.

The overall reaction for the thermal decomposition is:

2KCIO₃(I) → 2KCI(s) + 3O₂(g)

However, it takes place in the following steps:

Formation of potassium chlorate(VII) (potassium perchlorate), KCIO₄

4KCIO₃(I) → KCI(s) + 3KCIO₄(I)

Decomposition of potassium chlorate(VII)

KCIO₄(I) → KCI(s) + 2O₂(g)

An alternative set up is to clamp two test-tubes above the Bunsen burner so that they are heated equally. The catalyst and control tubes can then be done at the same time, this has a little more impact, but it is more difficult to convince the students that the heating of the two test-tubes is equal.

Alternative method for comparing catalysts

You may prefer to use equimolar quantities of the catalysts rather than equal masses.

Both sodium chlorate(V) and potassium chlorate(V) react at similar rates. There is very little difference in effectiveness between the catalysts.

Health & Safety checked, February 2008