Weird Science

Pyrophoric Iron

Polish ver­sion is here

The fol­lo­wing article was ori­gi­nally publi­shed in the jour­nal for edu­ca­tors Che­mia w Szkole (eng. Che­mi­stry in School) (1/2024):

Ilustracja

Ples M., Piro­fo­ryczne żelazo (eng. Pyro­pho­ric Iron), Che­mia w Szkole (eng. Che­mi­stry in School), 1 (2024), Agen­cja AS Józef Szew­czyk, pp. 48-49

How to Ignite Iron?

Iron Fe is a metal known since ancient times. In its pure form, it is a shiny, silvery, fairly hard, and rela­ti­vely high-mel­ting metal. Its mel­ting point is 1534.85°C (2794.73°F). Iron is brit­tle, which is why today it is most com­monly used in the form of alloys with car­bon C — cast iron and steel — as well as with other metals. These alloys are mecha­ni­cally stron­ger than pure iron and exhi­bit other desi­ra­ble pro­per­ties [1] [2]. Iron is also a trace ele­ment essen­tial for life, as it is a key com­po­nent of hemo­glo­bin [3].

Che­mi­cally, iron belongs to the group of rela­ti­vely reac­tive metals. It rea­dily reacts with acids, for­ming cor­re­spon­ding salts, and can oxi­dize with atmo­sphe­ric oxy­gen — even at room tem­pe­ra­ture.

We know that com­bu­stion is a rapid form of oxi­da­tion. So, is it pos­si­ble to actu­ally set iron on fire?

Ilustracja
Ani­ma­tion: sup­ple­men­tary mate­rial

Let’s Try It

Take any iron or steel object and heat it inten­sely in a bur­ner flame. After a while, a thin layer of oxide will form on the metal’s sur­face — but you cer­ta­inly won’t achieve igni­tion. Howe­ver, if you toss a pinch of fine steel filings into the flame, you’ll see beau­ti­ful, spar­kling fla­shes. These are rapi­dly bur­ning iron par­tic­les. Simi­larly, you can ignite steel or iron wool, com­monly used for poli­shing flo­ors or brass objects. It con­si­sts of extre­mely thin fila­ments that can easily catch fire, pro­du­cing a spec­ta­cu­lar display of sparks while rele­a­sing a signi­fi­cant amo­unt of heat (Photo 1).

Photo 1 – Bur­ning steel wool

Finely pow­de­ring the iron incre­a­ses its sur­face area, which impro­ves access to oxy­gen from the air and allows the par­tic­les to heat more effi­cien­tly — trig­ge­ring rapid oxi­da­tion. To burn iron, then, you sim­ply need to grind it finely eno­ugh. It turns out that iron with a suf­fi­cien­tly deve­lo­ped sur­face beco­mes pyro­pho­ric, mea­ning it can spon­ta­ne­o­u­sly ignite at room tem­pe­ra­ture.

Mate­rials Nee­ded

This time, all you need is one che­mi­cal com­po­und: iron(II) oxa­late FeC2O4. This com­po­und typi­cally appe­ars as a bri­ght yel­low pow­der (Photo 2).

Photo 2 – Iron(II) oxa­late

You can, of course, pur­chase iron(II) oxa­late from a che­mi­cal sup­plier, but pre­pa­ring it your­self is sim­ple eno­ugh to make it a rewar­ding expe­ri­ment in your own lab. For this syn­the­sis, you’ll need just two sub­stan­ces:

Oxa­lic acid is the sim­plest dicar­bo­xy­lic acid, and its dihy­drate form appe­ars as a white cry­stal­line pow­der. Iron(II) sul­fate hep­ta­hy­drate is typi­cally found as gre­e­nish cry­stals. Other well-solu­ble iron(II) salts can also be used. Nei­ther sub­stance is highly toxic, altho­ugh oxa­lic acid is irri­ta­ting and may have harm­ful effects if mishan­dled.

You’ll need to pre­pare con­cen­tra­ted solu­tions of both oxa­lic acid and iron(II) sul­fate, and then mix them toge­ther. The reac­tion pro­ce­eds faster when the mixture is gen­tly hea­ted; the liquid beco­mes clo­udy, and a yel­low pre­ci­pi­tate of poorly solu­ble iron(II) oxa­late begins to form and set­tle at the bot­tom. The reac­tion can be writ­ten as:

C2O42- + Fe2+ → FeC2O4

The pre­ci­pi­tate sho­uld be washed seve­ral times by decan­ta­tion, then fil­te­red and tho­ro­u­ghly dried. It's best to dry it at room tem­pe­ra­ture, as exces­sive heat may decom­pose the com­po­und.

Demon­stra­tion

Add a small amo­unt of tho­ro­u­ghly dried iron(II) oxa­late to a test tube. Don’t use too much — just eno­ugh to form a 1–2 cm (about 0.4–0.8 in) layer of pow­der (Photo 3).

Photo 3 – Sub­stance in the test tube

Now heat the tube using a spi­rit or gas bur­ner (Photo 4).

Photo 4 – Begin­ning the hea­ting pro­cess

After a short while, you’ll notice that water vapor begins to rise from the solid. This vapor con­den­ses on the coo­ler upper part of the test tube. It’s best to gen­tly heat this area too, to pre­vent con­den­sa­tion buil­dup.

Con­ti­nue hea­ting until the entire con­tents of the tube turn into a gray­ish-black pow­der (Photo 5).

Photo 5 – Color change of the pow­der

Now, plug the test tube with a small piece of glass wool and, while it is still warm, place it over a fire­proof sur­face (Photo 6A). In a dar­ke­ned room, open the test tube and pour the black pow­der out from a hei­ght. Upon con­tact with air, the sub­stance igni­tes, cre­a­ting a daz­zling cascade of orange-white sparks (Photo 6B).

Photo 6 – Final stage of the expe­ri­ment; A – pow­der ready to be pou­red, B – spon­ta­ne­ous igni­tion of the finely divi­ded iron mixture

Expla­na­tion

Iron(II) oxa­late is sta­ble at room tem­pe­ra­ture but decom­po­ses easily upon hea­ting. This decom­po­si­tion pro­du­ces water vapor, car­bon dio­xide, fine iron pow­der, and iron(II) oxide. The water esca­pes as steam, while a pyro­pho­ric mixture of ele­men­tal iron and iron(II) oxide rema­ins in the test tube. It doesn’t ignite imme­dia­tely because the gene­ra­ted car­bon dio­xide displa­ces the air in the tube. Once the pow­der is pou­red out and expo­sed to atmo­sphe­ric oxy­gen, the fol­lo­wing reac­tion occurs:

Fe + FeO + O2 → Fe2O3

The iron and iron(II) oxide oxi­dize into iron(III) oxide, rele­a­sing energy in the form of light and heat — and cre­a­ting the eye-cat­ching display of sparks.

Refe­ren­ces:

All pho­to­gra­phs and illu­stra­tions were cre­a­ted by the author.

The above text inc­lu­des minor edi­to­rial modi­fi­ca­tions com­pa­red to the ver­sion publi­shed in the jour­nal, aimed at sup­ple­men­ting and adap­ting it for online pre­sen­ta­tion.

Adden­dum

The result of the expe­ri­ment can be seen in the video:

Marek Ples

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