Of Ashes and Alkalis

Author(s):  
Peter Wothers

The name azote, proposed by Lavoisier and his colleagues, did not gain wide acceptance; nitrogen, meaning ‘nitre-former’, is the name now familiar to us. Modern chemists understand ‘nitre’ to mean ‘potassium nitrate’, one of the key ingredients of gunpowder, containing the elements potassium, oxygen, and nitrogen. However, although it dates back to antiquity, the name nitre initially referred to a completely different compound containing no nitrogen at all. It is the Latinized name, natrium, derived from this original use, that gives us the modern chemical symbol Na, for the element Humphry Davy named sodium. Travellers to modern-day northern Egypt may find themselves in a region known as the Nitrian Desert, or the Natron Valley—Wadi El Natrun. Here, ancient Egyptians would collect crude salt mixtures from certain lakes and use them for a variety of purposes, such as cleaning, making glass, embalming, and the preparation of medicines. The Egyptian word for the salt may be written ‘nṭry’ or ‘ntr’ (‘neter’), and it has survived for over three thousand years through variations including ‘neter’ (Hebrew), ‘nitron’ (Greek), ‘nitrum’(Latin), and more modern modifications ‘nether’, ‘niter’, ‘nitre’, ‘natrun’, and ‘natron’. Bartholomeus Anglicus, the thirteenth-century monk and author of De proprietatibus rerum (‘On the Properties of Things’), quotes Isidore of Seville from five hundred years earlier saying: ‘Nitrum hath ye name of the countrey of Nitria that is in Aegypt. Thereof is medicine made, & there with bodies and clothes be cleansed and washed.’ Whether the salt was actually named after the region or vice versa is not clear. Although its composition varied enormously, what distinguished nitre from common salt was the presence of significant proportions of sodium carbonate and sodium bicarbonate (sodium hydrogen carbonate). In addition to these carbonates, analyses of ancient samples, including that used in the embalming of the pharaoh Tutankhamun, who died in 1352 BC, also reveal large proportions of common salt (sodium chloride), sodium sulfate, and silica (silicon dioxide), with smaller proportions of calcium and magnesium carbonates and other minor impurities.

1960 ◽  
Vol 6 (3) ◽  
pp. 367-379 ◽  
Author(s):  
Jack McLachlan

Dunaliella tertiolecta Butcher was found to be a euryhaline organism which grew at salinities ranging from 3.75 to 120‰. All the conservative elements of sea water, with the exception of chlorine, were found necessary for growth of the alga. The minimum requirement for sodium was much greater than that for any other element, and it was not possible to substitute other monovalent cations for the minimum requirement. Also, the alga could tolerate high concentrations of sodium chloride. The potassium and sulphur concentrations of the medium could be reduced to very low levels. Dunaliella could also tolerate high concentrations of these two elements. The addition of lithium to the medium inhibited the growth of the alga. High concentrations of sodium could partially eliminate the inhibition due to lithium. The minimum concentrations of calcium and magnesium necessary for growth approached the concentrations found in fresh waters. Calcium and magnesium were inhibitory at high concentrations, but the inhibition at high concentrations could be prevented if a Mg/Ca ratio of 4 was maintained over a wide range of concentrations in the medium.


2021 ◽  
Vol 03 (06) ◽  
pp. 451-457
Author(s):  
Shaymaa Issam Alawi ALBALDAWI ◽  
Faten Hameed Qasim AL SARRAJI

Mineral Salts are One of the Most important Non-Metallic Chemicals that were widely available in ancient Iraq, and due to its many Uses in life Matters and for industrial purposes, it was Allocated in the Study of a Type of these Salts, which is Sodium Chloride salt (Table Salt), as there were Several Types, including: - Calcium Sulfate Sodium Silicate, Sodium Carbonate and Potassium Nitrate Because of the Importance of Sodium Chloride (salt) in Ancient Iraq and the lack of Studies that Dealt with it, we Chose it as a Subject for our Study, and we Relied on Many Arab, Translated and Foreign Sources, the most important of which are: -Levy, Martin, 1980 , Chemistry and Chemical Technology, translated by: Al-Mayahi and others, Dar Al-Rashid. - Potts ,D.,1987,'' ON Salt and salting gathering in Ancient Mesopotamia ''(JESHO), vol.27‎.


2013 ◽  
Vol 761 ◽  
pp. 157-160
Author(s):  
Zhen Lin Lu ◽  
Xiao Jie Rao ◽  
Xiao Feng Xu

The porous molybdenum was prepared by addition of pore forming agent and powder metallurgy method. The results show that the species and amount of pore forming agent are the primary influencing factors for the microstructures and properties of porous molybdenum. The pore shapes in porous molybdenum are regular and uniformly distributed. The porosity of porous molybdenum would be the largest and the transmission rate would be the best when sodium chloride was selected as pore forming agent. The compressive fracture strength of porous molybdenum would be more than 30MPa when the ammonium hydrogen carbonate was selected as pore formimg agent and its addition was 70 % (volume fraction). But the porosity would be the lowest.


Reactions ◽  
2011 ◽  
Author(s):  
Peter Atkins

I shall now introduce you to one of the simplest kinds of chemical reaction: precipitation, the falling out from solution of newly formed solid, powdery matter when two solutions are mixed together. The process is really very simple and, I have to admit, not very interesting. However, I am treating it as your first encounter with creating a different form of matter from two starting materials, so please be patient as there are much more interesting processes to come. I would like you to regard it as a warming-up exercise for thinking about and visualizing chemical reactions at a molecular level. Not much is going on, so the steps of the reaction are reasonably easy to follow. There isn’t much to do to bring about a precipitation reaction. Two soluble substances are dissolved in water, one solution is poured into the other, and—providing the starting materials are well chosen—an insoluble powdery solid immediately forms and makes the solution cloudy. For instance, a white precipitate of insoluble silver chloride, looking a bit like curdled milk, is formed when a solution of sodium chloride (common salt) is poured into a solution of silver nitrate. Now, as we shall do many times in this book, let’s imagine shrinking to the size of a molecule and watch what happens when the sodium chloride solution is poured into the silver nitrate solution. As you saw in my Preliminary remark, when solid sodium chloride dissolves in water, Na+ ions and Cl– ions are seduced by water molecules into leaving the crystals of the original solid and spreading through the solution. Silver nitrate is AgNO3; Ag denotes a silver atom, which is present as the positive ion Ag+; NO3– is a negatively charged ‘nitrate ion’, 1. Silver nitrate is soluble because the negative charge of the nitrate ion is spread over its four atoms rather than concentrated on one, 2, as it is for the chloride ion, and as a result it has rather weak interactions with the neighbouring Ag+ ions in the solid.


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