Oxygen and the lost world of giants

Author(s):  
David Beerling

Oxygen, in its molecular form, is the second most abundant gas in our atmosphere but second to none in courting controversy. Its discovery is often credited to the great experimenter Joseph Priestley (1733–1904), who in 1774 showed that heating red calyx of mercury (mercuric oxide) in a glass vessel by focusing sunlight with a hand lens produced a colourless, tasteless, odourless gas. Mice placed in vessels of the new ‘air’ lived longer than normal and candles burned brighter than usual. As Priestley noted in 1775, ‘on the 8th of this month I procured a mouse, and put it into a glass vessel containing two ounce measures of the air from my mercuric calcinations. Had it been common air, a full-grown mouse, as this was, would have lived in it about quarter of an hour. In this air, however, my mouse lived a full half hour.’ Later experiments revealed that mice actually lived about five times longer in the ‘new air’ than normal air, giving Priestley an early indication that air is about 20% oxygen. About the same time, the Swedish chemist Carl Scheele (1742–86), working in Uppsala, showed that air contained a mixture of two gases, one promoting burning (oxygen) and one retarding it (nitrogen). Like Priestley, Scheele had prepared samples of the gas that encouraged burning (‘fire air’) by heating mercuric oxide, and also by reacting nitric acid with potash and distilling the residue with sulfuric acid. However, by the time his findings were published in a book entitled the Chemical treatise on air and fire in 1777, news of Priestley’s discovery had already spread throughout Europe and the great English chemist lay claim to priority. Only later did it become clear from surviving notes and records that Scheele had beaten Priestley to it, producing oxygen at least two years earlier. The harsh lesson from history, which still rings true today, is that capitalizing on a new exciting discovery requires its expedient communication to your peers. The talented Scheele died at 43, his life shortened by working for much of the time with deadly poisons like gaseous hydrogen cyanide in poorly ventilated conditions.

Alloy Digest ◽  
2001 ◽  
Vol 50 (11) ◽  

Abstract Titanium shows outstanding resistance to seawater and marine atmospheres. It is also resistant to attack by hot metallic chloride solutions, sodium and potassium hypochlorite, and chlorine dioxide. The metal is resistant to attack by hot nitric acid at concentrations up to 80% and is not attacked by sulfuric acid. This datasheet provides information on composition, physical properties, hardness, elasticity, tensile properties, and bend strength as well as fatigue. It also includes information on high temperature performance and corrosion resistance as well as forming, heat treating, machining, and joining. Filing Code: TI-122. Producer or source: Timet.


2018 ◽  
Author(s):  
Harold Jeffrey M. Consigo ◽  
Ricardo S. Calanog ◽  
Melissa O. Caseria

Abstract Gallium Arsenide (GaAs) integrated circuits have become popular these days with superior speed/power products that permit the development of systems that otherwise would have made it impossible or impractical to construct using silicon semiconductors. However, failure analysis remains to be very challenging as GaAs material is easily dissolved when it is reacted with fuming nitric acid used during standard decapsulation process. By utilizing enhanced chemical decapsulation technique with mixture of fuming nitric acid and concentrated sulfuric acid at a low temperature backed with statistical analysis, successful plastic package decapsulation happens to be reproducible mainly for die level failure analysis purposes. The paper aims to develop a chemical decapsulation process with optimum parameters needed to successfully decapsulate plastic molded GaAs integrated circuits for die level failure analysis.


2000 ◽  
Vol 2000 (3) ◽  
pp. 106-107 ◽  
Author(s):  
C. Waterlot ◽  
B. Haskiak ◽  
D. Couturier

Various alkyl-substituted p-dimethoxybenzenes (ArH) react readily with nitric acid and sulfuric to form nitro-products (ArNO2). When the nitric acid is used in excess, the nitro-product react via either nitration to dinitro-compound (Ar(NO2)2) or via oxidative demethylation to nitro- p-quinone (Q). As such, the competition between the nitration, polynitration and oxidative dealkylation is effectively modulated by the added nitric acid and the alkyl-substituted p-dimethoxybenzenes.


Reactions ◽  
2011 ◽  
Author(s):  
Peter Atkins

Benzene, 1, is a hard nut to crack. The hexagonal ring of carbon atoms each with one hydrogen atom attached has a much greater stability than its electronic structure, with an alternation of double and single carbon–carbon bonds, might suggest. But for reasons fully understood by chemists, that very alternation, corresponding to a continuous stabilizing cloud of electrons all around the ring, endows the hexagon with great stability and the ring persists unchanged through many reactions. The groups of atoms attached to the ring, though, may come and go, and the reaction type responsible for replacing them is commonly ‘electrophilic substitution’. Whereas the missiles of Reaction 15 sniff out nuclei by responding to their positive electric charge shining through depleted regions of electron clouds, electrophiles, electron lovers, are missiles that do the opposite. They sniff out the denser regions of electron clouds by responding to their negative charge. Let’s suppose you want to make, for purposes you are perhaps unwilling to reveal, some TNT; the initials denote trinitrotoluene. You could start with the common material toluene, which is a benzene ring with a methyl group (–CH3) in place of one H atom, 2. Your task is to replace three of the remaining ring H atoms with nitro groups, –NO2, to achieve 3. And not just any of the H atoms: you need the molecule to have a symmetrical array of these groups because other arrangements are less stable and therefore dangerous. It is known that a mixture of concentrated nitric and sulfuric acids contains the species called the ‘nitronium ion’, NO2+, 4, and this is the reagent you will use. Before we watch the reaction itself, it is instructive to see what happens when concentrated sulfuric acid and nitric acid are mixed. If we stand, suitably protected, in the mixture, we see a sulfuric acid molecule, H2SO4, thrust a proton onto a neighbouring nitric acid molecule, HNO3. (Funnily enough, according to the discussion in Reaction 2, nitric ‘acid’ is now acting as a base, a proton acceptor! I warned you of strange fish in deep waters.) The initial outcome of this transfer is unstable; it spits out an H2O molecule which wanders off into the crowd. We see the result: the formation of a nitronium ion, the agent of nitration and the species that carries out the reaction for you.


1964 ◽  
Vol 207 (1) ◽  
pp. 169-172 ◽  
Author(s):  
Oliver Carrier ◽  
Meredith Cowsert ◽  
John Hancock ◽  
Arthur C. Guyton

Isolated arterial segments, 1 cm in length and 0.5–1.0 mm in diameter, were perfused with Tyrode's solution titrated to various levels of pH. Po2, Pco2, and temperature were held at physiological levels; the perfusion pressure was held at 100 mm Hg, and flow was measured by a drop counter. There was a linear increase in flow as the pH was decreased from 7.4, 0.05 units at a time, with an increase of 87% obtained at pH 7.15. As the pH was further decreased, the flow dropped until at pH 6.8 it leveled off slightly above control level. When the pH was raised, there was an initial 35% decrease in flow by the time pH 7.50 was reached, followed by an increase, reaching 50% above control level at 7.65. At still higher pHs a precipitous decrease in conductance occurred, flow leveling off slightly below control level at pH 7.80. Consistent results were obtained on 45 vessels using Tyrode's solution titrated to the desired pH with lactic acid, hydrochloric acid, acetic acid, sulfuric acid, nitric acid, sodium hydroxides, or sodium bicarbonate. These results indicate that vessels have a very narrow pH range in which they maintain physiological tone.


2019 ◽  
Vol 3 (2) ◽  
pp. 45 ◽  
Author(s):  
Jahromi ◽  
Ghahreman

Carbon-based catalysts can assist the oxidative leaching of sulfide minerals. Recently, we presented that AF 5 Lewatit® is among the catalysts with superior enargite oxidation capacity and capability to collect elemental sulfur on its surface. Herein, the effect of acid pre-treatment of the AF 5 catalyst was studied on the AF 5 surface, to further enhance the catalytic properties of AF 5. The AF 5 catalyst was pretreated by hydrochloric acid, nitric acid and sulfuric acid. The results showed that the acid treatment drastically changes the surface properties of AF 5. For instance, the concentration of quinone-like functional groups, which are ascribed to the catalytic properties of AF 5, is 45.4% in the sulfuric acid pre-treatment AF 5 and only 29.8% in the hydrochloric acid-treated AF 5. Based on the C 1s X-ray photoelectron spectroscopy (XPS) results the oxygenated carbon is 30.6% in the sulfuric acid-treated AF 5, 29.2% in the nitric acid-treated AF 5 and 28.3% in the hydrochloric acid-treated AF 5. The nitric acid pre-treated AF 5 resulted in the highest copper recovery during the oxidative enargite leaching process, recovering 98.8% of the copper. The sulfuric acid-treated AF 5 recovered 97.1% of the enargite copper into the leach solution. Among different leaching media and pre-treatment the lowest copper recovery was achieved with the HCl pre-treated AF 5 which was 88.6%. The pre-treatment of AF 5 with acids also had modified its elemental sulfur adsorption capacity, where the sulfur adsorption on AF 5 was increased from 30.9% for the HCl treated AF 5 to 51.1% for the sulfuric acid-treated AF 5.


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