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Evolution of Heat

Tin(II) oxide is a dark-coloured powder which oxidises spontaneously in air with the evolution of heat to give tin(IV) oxide, SnO, ... [Pg.192]

Cuprous cyanide solution. The most satisfactory method is to dissolve the cuprous cyanide (1 mol) in a solution of technical sodium cyanide (2 5-2-6 mols in 600 ml. of water). If it is desired to avoid the preparation of solid cuprous cyanide, the following procedure may be adopted. Cuprous chloride, prepared from 125 g. of copper sulphate crystals as described under 1 above, is suspended in 200 ml. of water contained in a 1-litre round-bottomed flask, which is fitted with a mechanical stirrer. A solution of 65 g. of technical sodium cyanide (96-98 per cent.) in 100 ml. of water is added and the mixture is stirred. The cuprous chloride passes into solution with considerable evolution of heat. As the cuprous cyanide is usually emplo3 ed in some modification of the diazo reaction, it is usual to cool the resulting solution in ice. [Pg.192]

Place 179 g. (109-5 ml.) of redistilled thionyl chloride in the 250 ml. Claisen flask and 51 g. (62-6 ml.) of n-hcxyl alcohol, b.p. 156-158°, in the separatory funnel. Add the nr-hexyl alcohol during 2 hours there is a slight evolution of heat, sulphur dioxide is evolved (hence carry out the... [Pg.274]

It has long been known that the adsorption of a gas on a solid surface is always accompanied by the evolution of heat. Various attempts have been made to arrive at a satisfactory thermodynamic analysis of heat of adsorption data, and within the past few years broad agreement has been achieved in setting up a general system of adsorption thermodynamics. Here we are not concerned with the derivation of the various thermodynamic functions but only with the more relevant definitions and the principles involved in the thermodynamic analysis of adsorption data. For more detailed treatments, appropriate texts should be consulted. " ... [Pg.13]

Anhydrous, monomeric formaldehyde is not available commercially. The pure, dry gas is relatively stable at 80—100°C but slowly polymerizes at lower temperatures. Traces of polar impurities such as acids, alkahes, and water greatly accelerate the polymerization. When Hquid formaldehyde is warmed to room temperature in a sealed ampul, it polymerizes rapidly with evolution of heat (63 kj /mol or 15.05 kcal/mol). Uncatalyzed decomposition is very slow below 300°C extrapolation of kinetic data (32) to 400°C indicates that the rate of decomposition is ca 0.44%/min at 101 kPa (1 atm). The main products ate CO and H2. Metals such as platinum (33), copper (34), and chromia and alumina (35) also catalyze the formation of methanol, methyl formate, formic acid, carbon dioxide, and methane. Trace levels of formaldehyde found in urban atmospheres are readily photo-oxidized to carbon dioxide the half-life ranges from 35—50 minutes (36). [Pg.491]

Polymerizations of methacrylic acid and derivatives are very energetic (MAA, 66.1 kj/mol MMA, 57.5 kJ/mol = 13.7 kcal/mol). The potential for the rapid evolution of heat and generation of pressure presents an explosion hazard if the materials are stored ia closed or poorly vented containers. [Pg.254]

Lewis Acid Complexes. Sulfolane complexes with Lewis acids, such as boron trifluoride or phosphoms pentafluoride (17). For example, at room temperature, sulfolane and boron trifluoride combine in a 1 1 mole ratio with the evolution of heat to give a white, hygroscopic soHd which melts at 37°C. The reaction of sulfolane with methyl fluoride and antimony pentafluoride inhquid sulfur dioxide gives crystalline tetrahydro-l-methoxythiophenium-l-oxidehexafluoroantimonate, the first example of an alkoxysulfoxonium salt (18). [Pg.69]

The reaction reverses when water is added to plaster of Paris and the mixture sets back to the dihydrate accompanied by a slight increase in volume and the evolution of heat. [Pg.407]

Handling and Storage. Cyanamide solution dimerizes to dicyandiamide and urea with the evolution of heat and a gradual increase in alkalinity accelerating the reaction. Storage above 30°C without pH stabilizer leads to excessive dimerization and can result in violent exothermic polymerization. Cyanamide should be stored under refrigeration and the pH tested periodically. Stabilized cyanamide can be kept at ambient temperature for a few weeks. [Pg.370]

Catalysts such as iron oxides cause isomeriza tion of the ethylene oxide to acetaldehyde with the evolution of heat. The acetaldehyde has a much lower autoignition temperature in air than does ethylene oxide, and the two effects may lead to hot-spot ignition (190,191). [Pg.465]

The thermal efficiency of the process (QE) should be compared with a thermodynamically ideal Carnot cycle, which can be done by comparing the respective indicator diagrams. These show the variation of temperamre, volume and pressure in the combustion chamber during the operating cycle. In the Carnot cycle one mole of gas is subjected to alternate isothermal and adiabatic compression or expansion at two temperatures. By die first law of thermodynamics the isothermal work done on (compression) or by the gas (expansion) is accompanied by the absorption or evolution of heat (Figure 2.2). [Pg.60]

At this point considerable evolution of heat occurs. A cold water bath should be kept in readiness for application to the reaction flask. [Pg.99]

Any substance, as presented for transport, which is liable to produce a dangerous evolution of heat or gas under the conditions normally encountered in air transport. [Pg.478]

Let a volume (dv) of mobile phase pass through the cell, carrying solute that is absorbed onto the surface of the adsorbent with the evolution of heat, and let the resulting temperature change be (d6). [Pg.220]

Cooler Absorbers When the absorption of a gas is accompanied by the evolution of heat, an important function of the absorption equipment is the removal of the heat generated. This may be accomplished by using a number of towers in series, the liquid from each tower being circulated through an external cooler. There are different types of cooler-absorbers in which processes of this type can be carried out in a single unit. The materials of which these cooler-absorbers are constructed should be of high thermal conductivity and resistant to corrosion by the substances used in the process. As an example, in the manufacture of hydrochloric acid of the... [Pg.246]

Chemical Reactivity - Reactivity with Water Moderate reaction with the evolution of heat Reactivity with Common Materials Rapidly absorbs moisture, forming hydrobromic acid. Highly corrosive to most metals, with the evolution of flammable and explosive hydrogen gas Stability During Transport Stable Neutralizing Agents for Acids and Caustics Flush with water and apply powdered limestone, slaked lime, soda ash, or sodium bicarbonate Polymerization Not pertinent Inhibitor of Polymerization Not pertinent. [Pg.204]

Ammonia is readily absorbed by H2O with considerable evolution of heat ( 37.1 kJ per mol of NH3 gas). Aqueous solutions are weakly basic... [Pg.423]

When ignited, N2H4 bums rapidly and completely in air with considerable evolution of heat (see Panel) ... [Pg.428]


See other pages where Evolution of Heat is mentioned: [Pg.164]    [Pg.106]    [Pg.182]    [Pg.261]    [Pg.320]    [Pg.369]    [Pg.730]    [Pg.865]    [Pg.943]    [Pg.977]    [Pg.166]    [Pg.167]    [Pg.255]    [Pg.475]    [Pg.168]    [Pg.68]    [Pg.1510]    [Pg.1654]    [Pg.2317]    [Pg.209]    [Pg.219]    [Pg.344]    [Pg.48]    [Pg.17]    [Pg.45]    [Pg.45]    [Pg.365]    [Pg.916]    [Pg.68]    [Pg.172]    [Pg.211]    [Pg.214]   


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Absorption or evolution of heat

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