Phase decomposition temperature

Ammonium nitrate decomposes into nitrous oxide and water. In the solid phase, decomposition begins at about I50°C (302°F) but becomes extensive only above the melting point (I70°C) (338°F). The reaction is first-order, with activation energy about 40 kcal/g mol (72,000 Btii/lb mol). Traces of moisture and Cr lower the decomposition temperature thoroughly dried material has been kept at 300°C (572°F). All oxides of nitrogen, as well as oxygen and nitrogen, have been detected in decompositions of nitrates. 

Cast material is stated to have a number average molecular weight of about 10. Whilst the Tg is about 104°C the molecular entanglements are so extensive that the material is incapable of flow below its decomposition temperature (approx. 170°C). There is thus a reasonably wide rubbery range and it is in this phase that such material is normally shaped. For injection moulding and extrusion much lower molecular weight materials are employed. Such polymers have a reasonable melt viscosity but marginally lower heat distortion temperatures and mechanical properties. 

Vapor-phase decomposition and collection (Figs 4.16 to 4.18) is a standardized method of silicon wafer surface analysis [4.11]. The native oxide on wafer surfaces readily reacts with isothermally distilled HF vapor and forms small droplets on the hydrophobic wafer surface at room temperature [4.66]. These small droplets can be collected with a scanning droplet. The scanned, accumulated droplets finally contain all dissolved contamination in the scanning droplet. It must be dried on a concentrated spot (diameter approximately 150 pm) and measured against the blank droplet residue of the scanning solution [4.67-4.69]. VPD-TXRF has been carefully evaluated against standardized surface analytical methods. The user is advised to use reliable reference materials [4.70-4.72]. 

A considerable amount of research has been conducted on the decomposition and deflagration of ammonium perchlorate with and without additives. The normal thermal decomposition of pure ammonium perchlorate involves, simultaneously, an endothermic dissociative sublimation of the mosaic crystals to gaseous perchloric acid and ammonia and an exothermic solid-phase decomposition of the intermosaic material. Although not much is presently known about the nature of the solid-phase reactions, investigations at subatmospheric and atmospheric pressures have provided some information on possible mechanisms. When ammonium perchlorate is heated, there are three competing reactions which can be defined (1) the low-temperature reaction, (2) the high-temperature reaction, and (3) sublimation (B9). 

The Avrami—Erofe ev equation, eqn. (6), has been successfully used in kinetic analyses of many solid phase decomposition reactions examples are given in Chaps. 4 and 5. For no substance, however, has this expression been more comprehensively applied than in the decomposition of ammonium perchlorate. The value of n for the low temperature reaction of large crystals [268] is reduced at a 0.2 from 4 to 3, corresponding to the completion of nucleation. More recently, the same rate process has been the subject of a particularly detailed and rigorous re-analysis by Jacobs and Ng [452] who used a computer to optimize curve fitting. The main reaction (0.01 < a < 1.0) was well described by the exact Avrami equation, eqn. (4), and kinetic interpretation also included an examination of the rates of development and of multiplication of nuclei during the induction period (a < 0.01). The complete kinetic expressions required to describe quantitatively the overall reaction required a total of ten parameters. 

Two examples are (1) the thermal, gas-phase decomposition of acetaldehyde at high temperatures and (2) the reaction of the hydrated 2-propylchromium ion with molecular oxygen in aqueous solution. The reactions and their rate laws are as follows ... 

Consider the gas-phase decomposition A B -b C in an isothermal tubular reactor. The tube i.d. is 1 in. There is no packing. The pressure drop is 1 psi with the outlet at atmospheric pressure. The gas flow rate is O.OSSCF/s. The molecular weights of B and C are 48 and 52, respectively. The entering gas contains 50% A and 50% inerts by volume. The operating temperature is 700°C. The cracking reaction is first order with a rate constant of 0.93 s . How long is the tube and what... 

A third category of syn eliminations involves pyrolytic decomposition of esters with elimination of a carboxylic acid. The pyrolysis of acetate esters normally requires temperatures above 400° C and is usually a vapor phase reaction. In the laboratory this is done by using a glass tube in the heating zone of a small furnace. The vapors of the reactant are swept through the hot chamber by an inert gas and into a cold trap. Similar reactions occur with esters derived from long-chain acids. If the boiling point of the ester is above the decomposition temperature, the reaction can be carried out in the liquid phase, with distillation of the pyrolysis product. 

Table 1 summarizes the catalysts physisorption properties, the MWCNTs yields and their maximum decomposition temperatures. MCM41 produces amorphous carbon phases with higher thermal stability. Some authors have obtained CNT using only the MCM41 as a template [11, 12] but the reaction was carrying out at higher temperatures and its CNT yield was lower than the one obtained with mesoporous catalyst containing metallic incorporation as in our work. 

At elevated temperatures, acetaldehyde (CH3CHO, A) undergoes gas-phase decomposition into methane and carbon monoxide. The reaction is second-order with respect to acetaldehyde, with kA = 22.2 L mol-1 min-1 at a certain T. Determine the fractional conversion of acetaldehyde that can be achieved in a 1500-L CSTR, given that the feed rate of acetaldehyde is 8.8 kg min-1, and the inlet volumetric flow rate is 2.5 m3 min-1. Assime T and P arc unchanged... 

Around 400 K there is a phase transition to a disordered but still cubic structure associated with the terminal oxygen atom in a WO4 tetrahedron which can migrate to another tetrahedron, thereby reversing the direction in which a pair of tetrahedra point. Nevertheless the same general atomic mechanisms are responsible for the negative thermal expansion up to the decomposition temperature. 

For temperatures in excess of 320 °C the gas-phase decomposition of anhydrous H0C103 (or of its dihydrate) is a homogeneous, unimolecular reaction close to its first-order limit at pressures in excess of 20 torr440. Levy440 obtained a value... 

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