Variable high-pressure and concentration study of cyclohexane pyrolysis at high temperatures

A high-pressure and temperature cyclohexane pyrolysis shock tube study was completed with the goal of extending the experimental cyclohexane pyrolysis data to pressures relevant to current and future combustors and to investigate whether ring contraction products observed in high-pressure, supercritical phase cyclohexane and cycloalkane pyrolysis experiments can form at matching, and higher, pressures in the gas phase. The experiments in the current work were completed over a range of 950–1650 K and at nominal pressures of 40, 100, and 200 bar. No alkylcyclopentanes, possible ring contraction products, were observed to form under the conditions of the current study. The production of methylenecyclopentane and 1,3-cyclopentadiene, and the other three cyclic species quantified: cyclohexene, benzene, and toluene, increased significantly with a substantial increase in the initial fuel concentration. Two sets of experimental data obtained at 200 bar were compared with a literature and laboratory-generated model. Both models had difficulty capturing the propadiene and propyne profiles, and the literature model significantly overestimated the benzene observed in the set of experiments completed with the more dilute fuel mixture. The literature model was able to better predict propadiene, propyne, and benzene product profiles in the 200 bar set of experiments, which used a higher concentration of fuel in the test gas. These results suggest that despite both cyclohexane and benzene being well-studied and important species in combustion chemistry, their reaction pathways and reaction rates would benefit from further refinement.     

Stabilization at high temperatures

A general detailed model of polymer oxidative degradation in the presence of a stabilizer-oxygen acceptor was considered. The motion of the degradation zone boundary and the sample lifetime were obtained for various conditions of the process. In particular, it is shown that within the given concentration immobile oxygen acceptor has the best stabilizing properties. The theoretical results are compared with the experimental data obtained by using two independent methods: polymer sample cracking and a change in the ESR signal. Good agreement between theory and experiment was obtained.     

X-Ray diffraction at high temperatures

Experimental equipment for X-ray diffraction at high temperatures is introduced and the possibility to directly observe the evolution of the atomic (geometric) structure as a function of temperature is discussed. Recent results on crystallization investigations of amorphous iron-based alloys and on the structural development in thin molybdenum sulphide films are given. The kinetics of the process was followed by means of time resolved experiments in both cases.     

Tunnelling-induced dipolar polarization at high temperatures

Tunnelling-induced dipolar polarization at room temperature is demonstrated experimentally for the first time. The experiment is a manifest high-temperature analogue of the Haupt effect, observed previously only at low temperatures.     

Inorganic gas chromatography at high temperatures

Summary The potential of gas chromatography as a separation method for inorganic compounds (organometallic complexes are excluded) is demonstrated. At temperatures up to 1200 K it is possible to separate a large number of elements as their halides, oxides or hydroxides if an inorganic compound of high melting point and low volatility is used as stationary phase. Examples of isothermal and temperature-programmed separations are given. The influences of temperature, column-length, stationary phase and reactive gas or reactive gas mixture on the separation are discussed.

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Zusammenfassung Die Eignung der Gaschromatographie zur Trennung anorganischer Verbindungen wurde gezeigt (metallorganische Komplexe sind dabei ausgenommen). Bei Temperaturen bis zu 1200 K läßt sich eine große Zahl von Elementen als Halogenide, Oxide oder Hydroxide trennen, wenn man eine anorganische Verbindung mit hohem Schmelzpunkt und geringer Flüchtigkeit als stationäre Phase anwendet. Beispiele isothermer und temperaturprogrammierter Trennungen wurden angegeben. Die Einflüsse der Temperatur, der Säulenlänge, der stationären Phase sowie der reaktiven Gase bzw. deren Mischungen auf den Trennungsvorgang wurden diskutiert.

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Presented at the International Symposium on Microchemical Techniques 1977, Davos, May 1977.     

Brownian coagulation at high concentration

Particle growth by Brownian coagulation at high concentration in the continuum regime is investigated by solving the Langevin dynamics (LD) equations for each particle trajectory of polydisperse suspensions. By monitoring the LD attainment of the self-preserving size distribution (SPSD), it is shown that the classic Smoluchowski collision frequency function is accurate for dilute particle volume fractions, phis, below 0.1%. At higher phis, coagulation is about 4 and 10 times faster than for the classic theory at phis = 10 and 20%, respectively. For complete particle coalescence upon collision, SPSDs develop even in highly concentrated suspensions (up to phis = 35%), as with dilute ones, but are broadened with increasing phis. At high particle concentration, an overall coagulation rate is proposed that reduces to the classic one at low concentration. Detailed collision frequency functions are also obtained at various phis values. Fractal-like agglomerates undergoing coagulation at constant fractal dimension attain an SPSD only temporarily because their effective volume fraction continuously increases, approaching gelation in the absence of restructuring or fragmentation.     

Equation of state of nitrogen (N2) at high pressures and high temperatures: molecular dynamics simulation

Nitrogen equation of state at pressures up to 30 GPa (300 kbars) and temperatures above 800 K was studied by molecular dynamics (MD) simulations. The dynamics of the N(2) molecules is treated in hard rotor approximation, i.e., it accounts both translational and rotational degrees of freedom. The rotational motion of the N(2) molecule is treated assuming constant moment of inertia of the nitrogen molecule. The new MD program fully accounts anisotropic molecular nitrogen interaction. The N(2)-N(2) interaction potential has been derived by van der Avoird et al. [J. Chem. Phys. 84, 1629 (1986)] using the results of high precision Hartree-Fock ab initio quantum mechanical calculations. The potential, fully accounts rotational symmetry of the N(2)-N(2) system, by employing 6-j Wigner symbols, i.e., preserving full rotational symmetry of the system. Various numerical algorithms were tested, in order to achieve the energy preservation during the simulation. It has been demonstrated that the standard Verlet algorithm was not preserving the energy for the standard MD time step, equal to 5x10(-16) s. Runge-Kutta fourth order method was able to preserve the energy within 10(-4) relative error, but it requires calculation of the force four times for each time step and therefore it is highly inefficient. A predictor-corrector method of the fifth order (PC5) was found to be efficient and precise and was therefore adopted for the simulation of the molecular nitrogen properties at high pressure. Singer and Fincham algorithms were tested and were found to be as precise as PC5 algorithm and they were also used in the simulation of the equation of state. Results of MD simulations are in very good agreement with the experimental data on nitrogen equation of state at pressures below 1 GPa (10 kbars). For higher pressures, up to 30 GPa (300 kbars), i.e., close to molecular nitrogen stability limit, determined by Nellis et al. [Phys. Rev. Lett. 85, 1262 (1984)], the obtained numerical results provide new data of the experimentally unexplored region. These data were formulated in the analytical form of pressure-density-temperature equation of state.     

Incubation in cyclohexene decomposition at high temperatures

A detailed master equation simulation has been carried out for the thermal unimolecular decomposition of C₆H₁₀ in a shock tube. At the highest temperatures studied experimentally [J. H. Kiefer and J. N. Shah, J. Phys. Chem., 91, 3024 (1987)], the average thermal vibrational energy is greater than the reaction threshold and therefore 〈ΔE〉 (up and down steps) is positive for molecules at that energy, rather than negative; the converse is true at lower temperatures. The calculated incubation time, in which the decomposition rate constant rises to 1/e of its steady state value, is found to be only weakly dependent on temperature (at constant pressure) between 1500 K and 2000 K and to depend almost exclusively on 〈ΔE〉_d (down steps, only), and not on collision probability model. Simulations of the experimental data show the magnitude of 〈ΔE〉_d depends weakly on assumed collision probability model, but is nearly independent of temperature. The second moment 〈ΔE〉^½ is found to be independent of both temperature and transition probability model. The experimental data are not very sensitive to the possible energy-dependence of 〈ΔE〉_d for a wide range of assumptions. It is concluded that the observed experimental “delay times” probably can be identified with the incubation time; further experiments are desirable to test this possibility and obtain more direct measures of the incubation time.     

The isomerization of cycloheptatriene at high temperatures

The isomerization of cycloheptatriene at high temperatures (800–1250°K) has been studied experimentally using a shock tube at high pressures and by very low-pressure pyrolysis in the intermediate-pressure region (the first direct use of the latter technique for an isomerization). Rate coefficients obtained are in accord with previous results at lower temperatures. The results are examined theoretically to account for weak-collision nonequilibrium effects. These corrections are found to be appreciable at the temperatures studied.     

Solvent-exfoliated graphene at extremely high concentration

We describe three related methods to disperse graphene in solvents with concentrations from 2 to 63 mg/mL. Simply sonicating graphite in N-methyl-2-pyrrolidinone, followed by centrifugation, gives dispersed graphene at concentrations of up to 2 mg/mL. Filtration of a sonicated but uncentrifuged dispersion gives a partially exfoliated powder that can be redispersed at concentrations of up to 20 mg/mL. However, this process can be significantly improved by removing any unexfolaited graphite from the starting dispersion by centrifugation. The centrifuged dispersion can be filtered to give a powder of exfoliated few-layer graphene. This powder can be redispersed at concentrations of at least 63 mg/mL. The dispersed flakes are ~1 μm long and ~3 to 4 layers thick on average. Although some sedimentation occurs, ~26-28 mg/mL of the dispersed graphene appears to be indefinitely stable.     

Soft- and hard-agglomerate aerosols made at high temperatures

Criteria for aerosol synthesis of soft-agglomerate, hard-agglomerate, or even nonagglomerate particles are developed on the basis of particle sintering and coalescence. Agglomerate (or aggregate) particles are held together by weak, physical van der Waals forces (soft agglomerates) or by stronger chemical or sintering bonds (hard agglomerates). Accounting for simultaneous gas phase chemical reaction, coagulation, and sintering during the formation and growth of silica (SiO2) nanoparticles by silicon tetrachloride (SiCl4) oxidation and neglecting the spread of particle size distribution, the onset of hard-agglomerate formation is identified at the end of full coalescence, while the onset of soft-agglomerate formation is identified at the end of sintering. Process conditions such as the precursor initial volume fraction, maximum temperature, residence time, and cooling rate are explored, identifying regions for the synthesis of particles with a controlled degree of agglomeration (ratio of collision to primary particle diameters).     

Concentrated electrolyte solutions at high temperatures and pressures

A survey is given of recent experimental results obtained from high-temperature, high-pressure investigations with water, aqueous solutions, and ionic fluids. Data on the static dielectric constant of water to 550°C and 5 kbar are given and discussed with respect to their relation to water structure. Infrared and Raman spectra of HDO in pure water have been obtained to 400°C and 4 kbar, which give information on hydrogen bonding. Xe–H₂O and CO₂–H₂O mixtures were investigated in the infrared. Ni(II) and Cu(II) complexes were investigated by absorption spectroscopy in aqueous solutions of high chloride content to 350°C and 2–6 kbar. The gas-liquid critical point of ammonium chloride was found at 880°C and 1635 bars. This fluid appears to be predominantly ionic even in the critical region. The possibility of converting pure polar fluids such as ammonia and water into concentrated ionic solutions by self-ionization at very high pressures is mentioned.This paper was presented at the symposium, The Physical Chemistry of Aqueous Systems, held at the University of Pittsburgh, Pittsburgh, Pennsylvania, June 12–14, 1972, in honor of the 70th birthday of Professor H. S. Frank.     

The features of iodine loss at high temperatures

Journal of Thermal Analysis and Calorimetry - A series of crystalline thiazoloquinolinium iodides has been studied using a combination of thermal analysis, mass and Raman spectroscopy techniques....     

pH,Definition and measurement at high temperatures

In this review paper, the NBS scale and its limitations are briefly discussed. The magnitude of liquid junction potentials and some calculated values are presented. The use of a molality scale for hydrogen electrode concentration cells at high temperatures is described, and results from measurements on ionization equilibria are summarized. Use of this scale is also recommended for certain circumstances with cells without liquid junction. As an alternative activity scale, use of the Pitzer ion-interaction treatment for ions is recommended for special cases. Finally, reference data are presented for _±HCl in HCl(aq) to 350°C and (HCl+NaCl)(aq) to 200°C that were derived by use of the Pitzer ion-interaction treatment.Presented at the Second International Symposium on Chemistry in High Temperature Water, Provo, UT, August 1991.     

Thermodynamics of sodium chloride solutions at high temperatures

Osmotic coefficients are reported from vapor-pressure-lowering measurements on sodium chloride solutions at concentrations from approximately 4m to saturation and at temperatures from 75° C to 300° C. In combination with previously reported measurements at lower concentrations, these results allow a correlation of free energies for the system NaCl–H₂O over a range of concentrations and temperatures that is unprecedented for any aqueous electrolyte. Activity coefficients and other thermodynamic quantities for both salt and water have been calculated for the complete range of concentrations and temperatures. Calculated heats of solution and standard partial molal entropies agree well with calorimetric determinations where comparison is possible. The excess partial molal entropy of the salt is informative concerning structural effects and their changes with temperature and concentration.Presented in part at the 160th National Meeting of the American Chemical Society, Chicago, Illinois, September 1970.     

Adsorption phenomena at high pressures and temperatures.

Equilibrium isotherms of adsorption of methane on crystalline Rho zeolite were measured with the use of a precision volumetric gravimetric setup that was developed for determining the equilibrium and Kinetic parameters of adsorption in the pressure range of 0.1–160 MPa and temperature range of 300–600 K. The method of determining the accessible volume of an adsorption system (free volume + micropore volume) and the micropore volume of a sorbent was used. Two independent methods for calculation of micropore volume on the basis of the isotherms of excess adsorption were used. The discrepancy in the results of the calculation of the micropore volume by three independent methods is within the limits of the calculation accuracy. An evaluation of a change in the isosteric heats of the excess and absolute adsorption of methane on Rho zeolite was carried out in relation to filling and temperature. An evaluaton of the adsorption volume above the outer surface of the zeolite crystals was performed. The results of experimental investigations of methane adsorption on Rho zeolite can be used to solve the problem of encapsulation of gases by solid sorbents. kg]Key words kw]adsorption kw]micropore volume kw]surface kw]isostere kw]heat kw]zeoliteFor Part 1 see Ref. I.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 568–573, March, 1996.     

A review of pH measurement at high temperatures

Measurement of pH in aqueous solutions at up to 300 degrees and 150-300 bar is reviewed. Potentiometric membrane electrodes are identified as the sensors giving the most immediate hope of being practical. Zirconia membranes work well above 200 degrees and in alkaline solution, whereas glass membranes are best up to 150 degrees and in acidic solutions. Both membranes are largely free from interferences. Metal-metal oxide electrodes offer poor prospects, deviating from the ideal Nernstian response at all temperatures and being susceptible to interference from many redox and complexing agents, but systems based on iridium oxide have some promise. The hydrogen electrode remains the standard for pH measurement, but its analytical application is limited by the need to know the hydrogen partial pressure. A practical solution to this problem has yet to be found, except in restricted and artificial circumstances. Palladium hydride electrodes may be useful up to about 200 degrees , but in hydrogen-saturated waters revert to being hydrogen electrodes in any case. Non-potentiometric pH measurements with semiconducting oxides have been shown to be possible, but there are many unanswered questions about possible interferences. Considerable extra instrumentation is required, compared with potentiometry. Fibre-optic sensors based on indicator dyes have been investigated at room temperature, and have the great merit of not requiring a reference electrode. They seem, however, prone to many interferences and have an inherently limited working range of approximately 2 pH. No measurements at high temperature have been reported. Improved reference electrodes for potentiometric systems are still needed, although there have been advances in the design of external pressure-compensated electrodes working at room temperature. The silver-silver chloride system is still the one most favoured. There has been little rigorous work on standard buffer solutions at above 100 degrees and none at above 200 degrees . Neutral and alkaline buffers are especially needed. The establishment of proper pH standards for high-temperature work would make the testing of sensors both speedier and more reliable. Doubtless because of the experimental difficulties involved, few measurements have actually been made at high temperature, and those in a rather restricted range of conditions. In particular, measurements in dilute, poorly buffered, solutions, which provide the most rigorous test of a system's capability, are completely lacking.     

Energy transfer in unimolecular reactions at high temperatures

The application of modern theories of energy transfer to unimolecular reactions taking place at very high temperatures is discussed. It is shown that the efficiency of energy transfer for both reactant–reactant and reactant–inert diluent collisions may be substantially smaller than the values determined experimentally at lower temperatures. Consequently at high temperatures unimolecular falloff effects, particularly in some shock-tube measurements, may be greater than has been believed hitherto. The application of these calculations to the unimolecular reactions of cyclopropane, cyclobutane, and cyclohexene at temperatures around 1300°K is discussed, and it is shown that under shock-tube conditions the apparent first-order rate coefficient may be at least ten times less than the high-pressure limiting value.     

煤灰在高温下的流变特性研究

为了研究煤灰在高温下的流变特性,以陕西神木煤、内蒙纳林沟煤、宁夏羊肠湾煤和山东南屯煤四种煤灰为样品,利用高温旋转黏度计,研究了高温下煤灰渣黏度和剪切应力随剪切速率的变化。实验结果表明,当实验温度高于煤灰的液相线温度时,其流型表现为牛顿流体;当温度低于液相线温度时,其流型逐渐由牛顿流体转变为非牛顿流体。其中,陕西神木煤和宁夏羊肠湾煤的煤灰样品在高温下表现为剪切增稠,随着温度的降低,由牛顿流体转变为屈服涨塑性流体;内蒙纳林沟煤和山东南屯煤的煤灰样品在高温下表现为剪切变稀,随着温度的降低,由牛顿流体转变为屈服假塑性流体。另外,随着温度的降低,由于液态煤灰中晶体的不断析出,使屈服应力逐渐增大,降低了煤灰的流动性。