Temperature accelerator

Dithiophosphates. These compounds (13) are made by reaction of an alcohol with phosphoms pentasulfide, then neutralization of the dithiophosphoric acid with a metal oxide. Like xanthates, dithiophosphates contain no nitrogen and do not generate nitrosamines during vulcanization. Dithiophosphates find use as high temperature accelerators for the sulfur vulcanization of ethylene—propylene—diene (EPDM) terpolymers. 

At temperatures above 50°C, irreversible hydrolysis to formate and ammonia becomes important. If the heat of reaction is not removed, the increased temperature accelerates the decomposition and can create high pressure in a closed vessel. 

The operating temperature also affects the fuel cell operating potential, A high operating temperature accelerates reaction rates but... 

The startup speed and temperature acceleration curves as shown in Figure 19-2 are one such safety measure. If the temperature or speed are not reached in a certain time span from ignition, the turbine will be shutdown. In the early days when these acceleration and temperature curves were not used, the fuel, which was not ignited, was carried from the combustor and then deposited at the first or second turbine nozzle, where the fuel combusted which resulted in the burnout of the turbine nozzles. After an aborted start the turbine must be fully purged of any fuel before the next start is attempted. To achieve the purge of any fuel residual from the turbine, there must be about seven times the turbine volume of air that must be exhausted before combustion is once again attempted. 

Is the second step of the overall reaction for R=Me (N-methylphthalimide + hydrazine —> phthalimide hydrazide + methylamine) exothermic or endothermic Will higher temperatures accelerate or inhibit the reaction Is the structure drawn above for phthalimide hydrazide its lowest-energy form or are either the imine or diimine tautomers preferred Compare energies for the hydrazide and imine and diimine tautomers. Examine the geometry of phthalimide hydrazide and any low energy tautomer, and draw the Lewis structure(s) that best describes it. Can your Lewis structures account for the energy differences Examine electrostatic potential maps for all three molecules. Which molecule(s) are stablized by favorable electrostatic interactions Which are destabilized Can this help explain the energy differences Elaborate. 

Older methods use a liquid phase process (Figure 10-11). ° New gas-phase processes operate at higher temperatures with noble metal catalysts. Using high temperatures accelerates the reaction (faster rate). The hydrogenation of benzene to cyclohexane is characterized by a highly exothermic reaction and a significant decrease in the product volume... 

Testing of metals for resistance to sulphide stress cracking at ambient temperatures Accelerated test procedures for screening atmospheric surface coating systems for offshore platforms and equipment... 

Each of these cases involves an accumulation of heat in the system which manifests higher temperature and pressure. The increased temperature accelerates the reactions further which subsequently adds even more heat to the system. 

The known changes in polyphenolic material have already been noted. Fermentation also results in slight loss of extractable caffeine. Decreases of 5 to 7% have been observed.31 Higher-than-normal fermentation times and temperatures accelerate this effect. The fate of caffeine made unavailable during fermentation is not definitely known. It has been demonstrated that caffeine interacts with polyphenols,80-81 so it is likely that the alkaloid becomes complexed with the most insoluble thearubigen fractions that do not become part of the beverage.31... 

Secondary crystallization occurs most readily in polymers that have been quench-cooled. Quenched samples have low degrees of crystallinity and thus have relatively large volumes of amorphous material. A pre-requisite for secondary crystallization is that the amorphous regions must be in the rubbery amorphous state. Increased temperature accelerates the rate of secondary crystallization. The new volumes of crystallinity that form during secondary crystallization are generally quite small, amounting to less than 10% of the crystalline volume created during primary crystallization. 

In addition, as can be seen in Table 12.1, increased temperature accelerated this process, and equilibrium was reached within 15-60min under reflux (Zechmeister 1944). 

S2C12, a by-product in the manufacture of carbon tetrachloride from carbon disulphide. Was used, dissolved in solvent naphtha, in the vulcanising of mbber by the cold cure process and the vapour cure process. The process was fraught with health and safety problems and has been superseded by low temperature accelerators and room temperature vulcanising (RTV) systems for silicone and polyurethane. 

Based on experimental results and a model describing the kinetics of the system, it has been found that the temperature has the strongest influence on the performance of the system as it affects both the kinetics of esterification and of pervaporation. The rate of reaction increases with temperature according to Arrhenius law, whereas an increased temperature accelerates the pervaporation process also. Consequently, the water content decreases much faster at a higher temperature. The second important parameter is the initial molar ratio of the reactants involved. It has to be noted, however, that a deviation in the initial molar ratio from the stoichiometric value requires a rather expensive separation step to recover the unreacted component afterwards. The third factor is the ratio of membrane area to reaction volume, at least in the case of a batch reactor. For continuous opera-... 

Keywords infrequent events transition-state theory accelerated dynamics hyperdynamics parallel-replica dynamics temperature-accelerated dynamics molecular dynamics bond-boost hyperdynamics parallel-accelerated dynamics Cu(100)... 

Sorensen, M.R., Voter, A.F. Temperature-accelerated dynamics for simulation of infrequent events. J. Chem. Phys. 2000, 112, 9599-606. 

Cogoni, M., Uberuaga, B.P., Voter, A.F., Colombo, L. Diffusion of small self-interstitial clusters in silicon temperature-accelerated tight-binding molecular dynamics simulations. Phys. Rev. B 2005, 71(12), 121203-1-1. 

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