Chemical Video Blog

Thermite

Thermite is a pyrotechnic composition of aluminium powder and a metal oxide which produces an aluminothermic reaction known as a thermite reaction. It is not an explosive, but can create short bursts of extremely high temperatures focused on a very small target for a short period of time.

Metals are capable of burning under the right conditions similar to the combustion process of wood or gasoline. In fact, rust is the oxidation of steel or iron at very slow rates. Thermite is a process in which the correct mixture of metallic fuels are combined and ignited. Ignition itself requires extremely high temperatures.

The aluminium is oxidized by the oxide of another metal, most commonly iron oxide (rust). The products are aluminium oxide, free elemental iron, and a large amount of heat. The reactants are commonly powdered and mixed with a binder to keep the material solid and prevent separation.

The reaction is used for thermite welding, often used to join rail tracks. Other metal oxides can be used, such as chromium oxide, to generate elementary metal. Copper thermite, using copper oxide, is used for creating electric joints in a process called cadwelding. Some thermite-like mixtures are used as pyrotechnic initiators such as fireworks. [source]

Thermite burning reaction:

2Al + Fe₂O₃ = Al₂O₃ + 2Fe

produces so much energy that even liquid nitrogen won't stop it. Can't believe? Watch it by yourself:

A Nice Poem to Lithium

Lithium is a chemical element with the symbol Li and atomic number 3. It is a soft alkali metal with a silver-white color. Under standard conditions, it is the lightest metal and the least dense solid element. Like all alkali metals, lithium is highly reactive, corroding quickly in moist air to form a black tarnish. For this reason, lithium metal is typically stored under the cover of oil.

According to theory, Lithium (mostly 7Li) was one of the few elements synthesized in the Big Bang, although its quantity has vastly decreased. The reasons for its disappearance and the processes by which new lithium is created continue to be important matters of study in astronomy. Lithium is the 33rd most abundant element on Earth, but due to its high reactivity only appears there naturally in the form of compounds. Lithium occurs in a number of pegmatitic minerals, but is also commonly obtained from brines and clays; on a commercial scale, lithium metal is isolated electrolytically from a mixture of lithium chloride and potassium chloride.

Trace amounts of lithium are present in the oceans and in some organisms, though it serves no apparent biological function in humans. Nevertheless, the neurological effect of the lithium ion Li+ makes some lithium salts useful as a class of mood stabilizing drugs. Lithium and its compounds have several other commercial applications, including heat-resistant glass and ceramics, high strength-to-weight alloys used in aircraft, and lithium batteries. Lithium also has important links to nuclear physics: the splitting of lithium atoms was the first man-made nuclear reaction, and lithium deuteride serves as the fusion fuel in staged thermonuclear weapons.

You wouldn't think, but there is a very nice poem devoted to Lithium:

Fun periodic table of chemical elements song

The periodic table of the chemical elements is a table that displays all known chemical elements in a systematic way. The elements in the periodic table are ordered by their atomic number (Z) and are arranged in periods (horizontal rows) and groups (vertical columns). The layout of the periodic table is designed to illustrate periodic trends, similarities and differences in the properties of the elements.

Source: periodic table of chemical elements

Can periodic table be fun? See by yourself:

Methyl ethyl ketone peroxide + H2SO4

Methyl ethyl ketone peroxide (MEKP) is an organic peroxide, a high explosive similar to acetone peroxide, and can be dangerous to synthesize. Unlike acetone peroxide, however, MEKP is a colorless, oily liquid at room temperature and pressure, while acetone peroxide is a white solid. It is slightly less sensitive to shock and temperature, and more stable in storage.
Dilute solutions of 30 to 60% MEKP are used in industry and by hobbyists as the catalyst which initiates the polymerization of polyester resins used in glass-reinforced plastic, and casting. For this application, MEKP is dissolved in dimethyl phthalate, cyclohexane peroxide, or diallyl phthalate to reduce sensitivity to shock. Benzoyl peroxide can be used for the same purpose.

MEKP is a severe skin irritant and can cause progressive corrosive damage or blindness.

What happens if a drop of H2SO4 is added to a pile MEKP?

Watch it by yourself:

Sodium on water

Video of the exothermic reaction between sodium and water.

Sodium is placed on the water containing phenolphthalein:

2Na + 2H2O = 2NaOH + H2

The reaction is highly exotermic and emerging hydrogen starts to burn on the air with a bright yellow flame (colored by traces of sodium):

2H2 + O2 = 2H2O

Sodium is a chemical element which has the symbol Na (Latin: natrium), atomic number 11, atomic mass 22.9898 g/mol, oxidation number +1. Sodium is a soft, silvery white, highly reactive element and is a member of the alkali metals within "group 1" (formerly known as 'group IA'). It has only one stable isotope, ²³Na. Sodium was first isolated by Sir Humphry Davy in 1807 by passing an electric current through molten sodium hydroxide. Sodium quickly oxidizes in air so it must be stored in an inert environment such as kerosene. Sodium is present in great quantities in the earth's oceans as sodium chloride. It is also a component of many minerals, and it is an essential element for animal life. As such, it is classified as a dietary inorganic macro-mineral.

Compared with other alkali metals, sodium is generally less reactive than potassium and more so than lithium, in accordance with "periodic law": for example, their reaction in water, chlorine gas, etc.; the reactivity of their nitrates, chlorates, perchlorates, etc. An exception to the periodic law is regarding sodium's density. The density of the elements are expected to increase down the group. However, potassium is less dense than sodium.

Owing to its high reactivity, sodium is found in nature only as a compound and never as the free element. Sodium reacts exothermically with water: small pea-sized pieces will bounce across the surface of the water until they are consumed by it, whereas large pieces will explode. While sodium reacts with water at room temperature, the sodium piece melts with the heat of the reaction to form a sphere, if the reacting sodium piece is large enough. The reaction with water produces very caustic sodium hydroxide and highly flammable hydrogen gas. These are extreme hazards (see Precautions section below). When burned in air, sodium forms sodium peroxide Na₂O₂, or with limited oxygen, the oxide Na₂O (unlike lithium, the nitride is not formed). If burned in oxygen under pressure, sodium superoxide NaO₂ will be produced.

When sodium or its compounds are introduced into a flame it will contribute a bright yellow.

In chemistry, most sodium compounds are considered soluble but nature provides examples of many insoluble sodium compounds such as the feldspars. There are other insoluble sodium salts such as sodium bismuthate NaBiO₃, sodium octamolybdate Na₂Mo₈O₂₅• 4H₂O, sodium thioplatinate Na₄Pt₃S₆, sodium uranate Na₂UO₄. Sodium meta-antimonate's 2NaSbO₃•7H₂O solubility is 0.3g/L as is the pyro form Na₂H₂Sb₂O₇• H₂O of this salt. Sodium metaphosphate NaPO₃ has a soluble and an insoluble form.

Sodium ions are necessary for regulation of blood and body fluids, transmission of nerve impulses, heart activity, and certain metabolic functions. Interestingly, sodium is needed by animals, which maintain high concentrations in their blood and extracellular fluids, but the ion is not needed by plants. A completely plant-based diet, therefore, will be very low in sodium. This requires some herbivores to obtain their sodium from salt licks and other mineral sources. The animal need for sodium is probably the reason for the highly-conserved ability to taste the sodium ion as "salty." Receptors for the pure salty taste respond best to sodium, and otherwise only to a few other small monovalent cations (Li⁺, NH₄⁺, and to some extent also K⁺). Calcium chloride also tastes somewhat salty, but also quite bitter.

The most common sodium salt, sodium chloride (table salt), used for seasoning (for example the English word "salad" refers to salt) and warm-climate food preservation, such as pickling and making jerky (the high osmotic content of salt inhibits bacterial and fungal growth). As such, salt has been an important commodity in human activities (the English word salary refers to salarium, the perquisite ("perk") given to Roman soldiers for the purpose of buying salt). The human requirement for sodium in the diet is less than 500 mg per day, which is typically less than a tenth as much as many diets "seasoned to taste." Most people consume far more sodium than is physiologically needed. For certain people with salt-sensitive blood pressure, this extra intake may cause a negative effect on health.

Sodium (the English word for which is soda) has long been recognized in compounds, but was not isolated until 1807 by Sir Humphry Davy through the electrolysis of caustic soda. In medieval Europe a compound of sodium with the Latin name of sodanum was used as a headache remedy.

Sodium's chemical abbreviation Na was first published by Jöns Jakob Berzelius in his system of atomic symbols (Thomas Thomson's Annals of Philosophy^[2]) and is a contraction of the element's new Latin name natrium which refers to natron, a natural mineral salt whose primary ingredient is hydrated sodium carbonate and which historically had several important industrial and household uses later eclipsed by soda ash, baking soda and other sodium compounds.

Sodium imparts an intense yellow color to flames. As early as 1860, Kirchhoff and Bunsen noted the high sensitivity that a flame test for sodium could give. They state in Annalen der Physik und der Chemie in the paper "Chemical Analysis by Observation of Spectra":

In a corner of our 60 cu.m. room farthest away from the apparatus, we exploded 3 mg. of sodium chlorate with milk sugar while observing the nonluminous flame before the slit. After a while, it glowed a bright yellow and showed a strong sodium line that disappeared only after 10 minutes. From the weight of the sodium salt and the volume of air in the room, we easily calculate that one part by weight of air could not contain more than 1/20 millionth weight of sodium.

Sodium is relatively abundant in stars and the D spectral lines of this element are among the most prominent in star light. Sodium makes up about 2.6% by weight of the Earth's crust making it the fourth most abundant element overall and the most abundant alkali metal.

At the end of the 19th century, sodium was chemically prepared by heating sodium carbonate with carbon to 1100 °C.

Na₂CO₃ (liquid) + 2 C (solid, coke) → 2 Na (vapor) + 3 CO (gas).

It is now produced commercially through the electrolysis of liquid sodium chloride. This is done in a Downs Cell in which the NaCl is mixed with calcium chloride to lower the melting point below 700 °C. As calcium is less electronegative than sodium, no calcium will be formed at the cathode. This method is less expensive than the previous Castner process of electrolyzing sodium hydroxide.

Very pure sodium can be isolated by thermal decomposition sodium azide.

Metallic sodium costs about 15 to 20 US cents per pound (US$0.30/kg to US$0.45/kg) in 1997 but reagent grade (ACS) sodium cost about US$35 per pound (US$75/kg) in 1990.

Under extreme pressure, sodium departs from common melting behavior. Most materials require higher temperatures to melt under pressure than they do at normal atmospheric pressure. This is because they expand on melting due to looser molecular packing in the liquid, and thus pressure forces equilibrium in the direction of the denser solid phase.

At a pressure of 30 gigapascals (300,000 times sea level atmospheric pressure), the melting temperature of sodium begins to drop. At around 100 gigapascals, sodium will melt at near room temperature. A possible explanation for the aberrant behavior of sodium is that this element has one free electron that is pushed closer to the other 10 electrons when placed under pressure, forcing interactions that are not normally present. While under pressure, solid sodium assumes several odd crystal structures suggesting that the liquid might have unusual properties such as superconduction or superfluidity.

Sodium chloride or halite, better known as common salt, is the most common compound of sodium, but sodium occurs in many other minerals, such as amphibole, cryolite, soda niter and zeolite. Sodium compounds are important to the chemical, glass, metal, paper, petroleum, soap, and textile industries. Hard soaps are generally sodium salt of certain fatty acids (potassium produces softer or liquid soaps).

The sodium compounds that are the most important to industries are common salt (NaCl), soda ash (Na₂CO₃), baking soda (NaHCO₃), caustic soda (NaOH), Chile saltpeter (NaNO₃), di- and tri-sodium phosphates, sodium thiosulfate (hypo, Na₂S₂O₃ · 5H₂O), and borax (Na₂B₄O₇ · 10H₂O).

There are thirteen isotopes of sodium that have been recognized. The only stable isotope is ²³Na. Sodium has two radioactive cosmogenic isotopes (²²Na, half-life = 2.605 years; and ²⁴Na, half-life ≈ 15 hours).

Acute neutron radiation exposure (e.g., from a nuclear criticality accident) converts some of the stable ²³Na in human blood plasma to ²⁴Na. By measuring the concentration of this isotope, the neutron radiation dosage to the victim can be computed.

Extreme care is required in handling elemental/metallic sodium. Sodium is potentially explosive in water (depending on quantity) and is a caustic poison, since it is rapidly converted to sodium hydroxide on contact with moisture. The powdered form may combust spontaneously in air or oxygen. Sodium must be stored either in an inert (oxygen and moisture free) atmosphere (such as nitrogen or argon), or under a liquid hydrocarbon such as mineral oil or kerosene.

The reaction of sodium and water is a familiar one in chemistry labs, and is reasonably safe if amounts of sodium smaller than a pencil eraser are used and the reaction is done behind a plastic shield by people wearing eye protection. However, the sodium-water reaction does not scale up well, and is treacherous when larger amounts of sodium are used. Larger pieces of sodium melt under the heat of the reaction, and the molten ball of metal is buoyed up by hydrogen and may appear to be stably reacting with water, until splashing covers more of the reaction mass, causing thermal runaway and an explosion which scatters molten sodium, lye solution, and sometimes flame. This behavior is unpredictable, and among the alkali metals it is usually sodium which invites this surprise phenomenon, because lithium is not reactive enough to do it, and potassium is so reactive that chemistry students are not tempted to try the reaction with larger potassium pieces.

Sodium is much more reactive than magnesium; a reactivity which can be further enhanced due to sodium's much lower melting point. When sodium catches fire in air (as opposed to just the hydrogen gas generated from water by means of its reaction with sodium) it more easily produces temperatures high enough to melt the sodium, exposing more of its surface to the air and spreading the fire.

Few common fire extinguishers work on sodium fires. Water, of course, exacerbates sodium fires, as do water-based foams. CO₂ and Halon are often ineffective on sodium fires, which reignite when the extinguisher dissipates. Among the very few materials effective on a sodium fire are Pyromet and Met-L-X. Pyromet is a NaCl/(NH₄)₂HPO₄ mix, with flow/anti-clump agents. It smothers the fire, drains away heat, and melts to form an impermeable crust. This is the standard dry-powder canister fire extinguisher for all classes of fires. Met-L-X is mostly sodium chloride, NaCl, with approximately 5% Saran plastic as a crust-former, and flow/anti-clumping agents. It is most commonly hand-applied, with a scoop. Other extreme fire extinguishing materials include [[Lith⁺]], a graphite based dry powder with an organophosphate flame retardant; and [[Na⁺]], a Na₂CO₃-based material.

Because of the reaction scale problems discussed above, disposing of large quantities of sodium (more than 10 to 100 grams) must be done through a licensed hazardous materials disposer. Smaller quantities may be broken up and neutralized carefully with ethanol (which has a much slower reaction than water), or even methanol (where the reaction is more rapid than ethanol's but still less than in water), but care should nevertheless be taken, as the caustic products from the ethanol or methanol reaction are just as hazardous to eyes and skin as those from water. After the alcohol reaction appears complete, and all pieces of reaction debris have been broken up or dissolved, a mixture of alcohol and water, then pure water, may then be carefully used for a final cleaning. This should be allowed to stand a few minutes until the reaction products are diluted more thoroughly and flushed down the drain. The purpose of the final water soak and wash of any reaction mass which may contain sodium is to ensure that alcohol does not carry unreacted sodium into the sink trap, where a water reaction may generate hydrogen in the trap space which can then be potentially ignited, causing a confined sink trap explosion.

One notable atomic spectral line of sodium vapor is the so-called D-line. The D-line is one of the classified Fraunhofer lines observed in the visible spectrum of the sun's electromagnetic radiation. Sodium vapor in the upper layers of the sun creates a dark line in the emitted spectrum of electromagnetic radiation by absorbing visible light in a band of wavelengths around 589.5 nm. This wavelength corresponds to transitions in atomic sodium in which the valence-electron transitions from a 3p to 3s electronic state. Closer examination of the visible spectrum of atomic sodium reveals that the D-line actually consists of two lines called the D₁ and D₂ lines at 589.8 nm and 589.2 nm, respectively. This fine structure results from a spin-orbit interaction of the valence electron in the 3p electronic state. The spin-orbit interaction couples the spin angular momentum and orbital angular momentum of a 3p electron to form two states that are respectively notated as and in the LS coupling scheme. The 3s state of the electron gives rise to a single state which is notated as 3s(²S_{1 / 2}) in the LS coupling scheme. The D₁-line results from an electronic transition between 3s(²S_{1 / 2}) lower state and upper state. The D₂-line results from an electronic transition between 3s(²S_{1 / 2}) lower state and upper state. Even closer examination of the visible spectrum of atomic sodium would reveal that the D-line actually consists of a lot more than two lines. These lines are associated with hyperfine structure of the 3p upper states and 3s lower states. Many different transitions involving visible light near 589.5 nm may occur between the different upper and lower hyperfine levels.

from Wikipedia

Nitroglycerin explosion

Nitroglycerin (NG), also known as nitroglycerine, trinitroglycerin, and glyceryl trinitrate, is a chemical compound. It is a heavy, colorless, oily, explosive liquid obtained by nitrating glycerol. It is used in the manufacture of explosives, specifically dynamite, and as such is employed in the construction and demolition industries, and as a plasticizer in some solid propellants. It is also used medically as a vasodilator to treat heart conditions. Nitroglycerin is a venous dilator that decreases preload.

In its pure form, it is a contact explosive (physical shock can cause it to explode) and degrades over time to even more unstable forms. This makes it highly dangerous to transport or use. In this undiluted form it is one of the most powerful high explosives, comparable to the military explosives RDX and PETN (which are not used in munitions at full concentration because of their sensitivity) as well as the plastic explosive C-4.

Early in the history of this explosive it was discovered that liquid nitroglycerin can be "desensitized" by cooling to 5 to 10 °C (40 to 50 °F), at which temperature it freezes, contracting upon solidification. However, later thawing can be extremely sensitizing, especially if impurities are present or if warming is too rapid. It is possible to chemically "desensitize" nitroglycerin to a point where it can be considered approximately as "safe" as modern high explosive formulations, by the addition of approximately 10-30% ethanol, acetone, or dinitrotoluene (percentage varies with the desensitizing agent used). Desensitization requires extra effort to reconstitute the "pure" product. Failing this, it must be assumed that desensitized nitroglycerin is substantially more difficult to detonate, possibly rendering it useless as an explosive for practical application.

A serious problem in the use of nitroglycerin results from its high freezing point (13 °C [55 °F]). Solid nitroglycerin is much less sensitive to shock than the liquid, a feature common in explosives; in the past it was often shipped in the frozen state, but this resulted in a high number of accidents during the thawing process by the end user just prior to use. This disadvantage is overcome by using mixtures of nitroglycerin with other polynitrates; for example, a mixture of nitroglycerin and ethylene glycol dinitrate freezes at -29 °C (-20 °F).

Nitroglycerin and any or all of the dilutents used can certainly deflagrate or burn. However, the explosive power of nitroglycerin is derived from detonation: energy from the initial decomposition causes a pressure gradient that detonates the surrounding fuel. This can generate a self-sustained shock-wave that propagates through the fuel-rich medium at or above the speed of sound as a cascade of near-instantaneous pressure-induced decomposition of the fuel into gas. This is quite unlike deflagration, which depends solely upon available fuel, regardless of pressure or shock.

Nitroglycerin is prepared by nitration of glycerol (also known as glycerin). In the process, glycerin is slowly tipped into a mix of full concentration nitric acid and sulfuric acid (about 50% sulfuric acid, 40% nitric acid, and 5-10% glycerin). The mixed acid must be cooled to approximately room temperature before the glycerin is added because they will exotherm (heat up) greatly when combined. The solution is slowly stirred. A few seconds after mixing, the vessel must be immersed in a jacket of ice water to prevent the exothermic reaction from overheating it, causing nitric acid decomposition or even an explosion. The temperature should never exceed 10 °C (50 °F), but the chemicals must not be cooled by the ice water before mixing, or the nitrating reaction will not take place.

If the reaction is successful, the nitroglycerin will form a slightly yellow or straw colored liquid which will float to the top of the acid mix. The mix is then carefully poured into a large container of water. The nitroglycerin will settle to the bottom (it is water insoluble) and should be neutralized with sodium carbonate and water mix until its pH becomes neutral.

Another method of producing nitroglycerin is to mix the glycerin and sulfuric acid first, which produces heat, but at this stage is not dangerous. After cooling, the nitric acid can be added reasonably quickly to the mix, but it can still cause uncontrolled nitration. It can also cause the acid to splash. Therefore it should be avoided, and the nitration mixture should be added very slowly to the glycerol. The then nitrated glycerin and acid solution has to be left for the nitroglycerin to float to the top, since this method can sometimes produce the nitroglycerin in fine quantities. The waiting period is a day or less, but the prolonged exposure to the acids may cause the decomposition or even the explosion of the nitroglycerin, although the latter will only occur in large batches. If a milky colour is seen, it is only because of water in the mix. From this point, continue as above. This method was used in the time of Nobel, although it was not his own.

The industrial manufacturing process often uses a nearly 50:50 mixture of sulfuric acid and nitric acid. This can be produced by mixing white fuming nitric acid (quite costly pure nitric acid in which oxides of nitrogen have been removed, as opposed to red fuming nitric acid) and concentrated sulfuric acid. More often, this mixture is attained by the cheaper method of mixing fuming sulfuric acid (sulfuric acid containing excess sulfur trioxide) and azeotropic nitric acid (consisting of around 70% nitric acid, the rest being water).

The sulfuric acid produces protonated nitric acid species, which are attacked by glycerin's nucleophilic oxygen atoms. The nitro group is thus added as an ester C-O-NO2 and water is produced. This is different from an aromatic nitration reaction in which nitronium ions are the active species in an electrophilic attack of the molecules ring system.

The addition of glycerin results in an exothermic reaction (i.e., heat is produced), as usual for mixed acid nitrations. However, if the mixture becomes too hot, it results in runaway, a state of accelerated nitration accompanied by the destructive oxidizing of organic materials of nitric acid and the release of very poisonous brown nitrogen dioxide gas at high risk of an explosion. Thus, the glycerin mixture is added slowly to the reaction vessel containing the mixed acid (not acid to glycerin). The nitrator is cooled with cold water or some other coolant mixture and maintained throughout the glycerin addition at about 22 °C, much below which the esterification occurs too slowly to be useful. The nitrator vessel, often constructed of iron or lead and generally stirred with compressed air, has an emergency trap door at its base, which hangs over a large pool of very cold water and into which the whole reaction mixture (called the charge) can be dumped to prevent an explosion, a process referred to as drowning. If the temperature of the charge exceeds about 10 °C (actual value varying by country) or brown fumes are seen in the nitrators vent, then it is immediately drowned.

Because of the great dangers associated with its production, most nitroglycerin production facilities are in offshore rigs or very remote locations.

from Wikipedia

Acetone peroxide explosion

Video of the acetone peroxide explosion.

Acetone peroxide (triacetone triperoxide, peroxyacetone, TATP, TCAP) is an organic peroxide and a primary high explosive. It takes the form of a white crystalline powder with a distinctive acrid smell. It is highly susceptible to heat, friction, and shock. For its instability, it has been called the "Mother of Satan". It has perhaps sprung into notoriety due to its alleged use in the July 2005 London bombings and has also been reported as the explosive favored by suspects arrested on August 10, 2006 who allegedly intended to destroy aeroplanes flying from the United Kingdom to the United States. Acetone peroxide was discovered in 1895 by Richard Wolffenstein. He was the first chemist who used inorganic acids as a catalyst. He was also the first researcher who received a patent for using the peroxide as an explosive compound. In 1900 Bayer and Villiger described in some articles in the same journal the first synthesis of the dimer and used acids for the synthesis of both peroxides too. Information about it including the relative proportions of monomer, dimer, and trimer is also available an article of Milas and Golubović. Other sources include crystal structure and 3d analysis in "The Chemistry of Peroxides" edited by Saul Patai (pp. 396–7), as well as the "Textbook of Practical Organic Chemistry" by Vogel. (from wikipedia)

Magnesium burning and reacting with water

Video of magnesium burning and then reacting with water vapors:

2 Mg + O2 = 2 MgO

Mg + H2O = MgO + H2

Emerging hydrogen consequently burns in the air with a big flame:

2 H2 + O2 = 2 H2O

Sodium burning in chlorine

Video of sodium burning in chlorine and producing sodium chloride:
2Na + Cl2 = 2NaCl

Thermite burning

Video of burning thermite.

The reaction Fe2O3 + 2Al = 2Fe + Al2O3 is so exotemric that produced iron is in liquid state.

Tremendous Ammonium Perchlorate Explosion near Las Vegas

Sulfur burning in air and in pure oxygen

Liquid Nitrogen Into A Swimming Pool

An exotermic reaction: potassium nitrate + sugar

Explosive chemical reaction: potassium + bromine