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Process parameters total yield

Conjugated dehydrogenation of isopropylbenzene was planned [87] by the method of experiments with the minimal number of tests. Total yields of styrene and a-methylstyrene per injected isopropylbenzene were taken for optimized parameters, because these monomers are equally valuable. At the gradient motion (T = 640 °C) the highest yield of the target products (styrene + a-methylstyrene) equaled 56.8% with about 90% selectivity. Further gradient motion was of no practical interest due to a process selectivity decrease down to 80%. [Pg.113]

In the total interaction diagram of Fig. 13.6, as the system yields for reactive extrusion, several positive feedback loops can be distinguished, due to which a disturbance in a process parameter can be amplified which may lead to an unstable operation. In this way, three different possible sources of instabilities can be distinguished ... [Pg.405]

We can observe in Table 5.43 that the maximum yield is obtained with catalyst number two (X2 = 2), the response obtained with this catalyst can be analyzed deeply with respect to other process parameters such as the input reactor gas flow rate and the temperature. Two different values or levels of these parameters will be considered whereas other parameters or factors will remain constant (Table 5.40). Table 5.47 gives the experimental data after the arrangement required by Table 5.45 together with the partial and total mean values of SO2 oxidation degree. [Pg.424]

ABSTRACT The purpose of this study is to find pyrolysis conditions for diromium-copper- arsenate (CCA) treated wood in ordw to maxiniize the retention of arsenic in wood charcoal along with a high oil yield. An experimental dlhy was built to examine the influence of process parameters such as pyrolysis temperature and total pyrolysis time. Milled powder was prepared from CCA treated wood. The powder was pyrolized on top of the fluidized bed at temperatures between 300 to 500 C and during total pyrolysis times of 80 to 3600 s. [Pg.1396]

For alkenes more difficult to reduce than CO2, such as butadiene (63a), electron transfer from C02 to the alkene may be involved. Cross-coupling of CO2 and 63a in MeCN has been carried out in an undivided flow cell at constant current. Using Et4N salts of formate or oxalate as supporting electrolyte, the anode process is formation of CO2 and H" ", which are both consumed in the cathode process [167]. The outcome (up to 63% total yield) was a mixture of isomers of C5, Cg, and Cjo unsaturated carboxylic acids and diacids. The detailed mechanism is not known, but the products may arise from initial addition of C02 to the unreduced butadiene [167], although electron transfer from C02 to 63a or direct reduction of 63a (present in large excess) cannot be ruled out. Based on the observed influence of experimental parameters on the distribution of the C5, Cg, and C]o acid products, the authors suggest that the reactions take place between adsorbed intermediates [167]. [Pg.840]

Both the time-on-stream and the reactant ratio are important chemical engineering parameters affecting the characteristics of the process. It was found that the increase in the time-on-stream at T = 673K can improve both the conversion of ethane and the yield of ethylene. The total yield of chloroorganic products therewith decreases, but the concentration of vinyl chloride passes through a maximum. We also observed an increase in the yield of deep oxidation products COx (see Table 2). [Pg.312]

To scale up a chemical process to pilot or commercial-scale operations, a significant laboratory effort is required to define the operating ranges of the critical process parameters. A critical process parameter is any process variable that may potentially affect the product quality or yield. This information is required to prepare a Process Risk Analysis, which is an FDA prerequisite for process validation. Process parameters that are often evaluated as part of the risk analysis include reaction temperature, solvent systems, reaction time, raw material and reagent ratios, rate and orders of addition, agitation, and reaction concentration. If catalysts are employed as part of the process, additional laboratory evaluation may also be required to further define the process limits. Experimental design is often used for the evaluation of critical process parameters to minimize the total laboratory effort (4). [Pg.411]

The model equations employing biokinetics of Groot et al. and PV data of Gudernatsch et al. were solved using an iterative procedure in a computer program to optimize process parameters for minimum total cost. The hybrid PV + distillation process yields better utilization of the sugar in the feed because of decrease in inhibition. The results indicated that the raw material and membrane fixed cost contribute more than 80% of the direct production cost. Further, the direct production cost of EtOH cost for the hybrid process was found to be 12%-16% lower than the conventional process. [Pg.203]

Economic evaluation - one main challenge is to bring MES out of the laboratory to technical application. At the early stage of the development, a rough calculation should at least include the assessment of needed productivities at the given fixed and variable costs (e.g., for reactor, electrodes, membranes, reaction medium, pretreatment of the gas). The volumetric productivities (space-time yields), final product concentrations, and total process times determine the overall process performance. These parameters should be used to define operational windows for the production of bulk chemicals. Furthermore, this theoretical approach allows the identification of limiting process parameters. [Pg.1276]

The economic feasibility of enzymatic production of biodiesel depends on a series of factors. These factors mainly include (1) the raw material costs such as the prices of oil feedstock, alcohol and enzyme (2) the process parameters, such as oil-to-biodiesel conversion ratio, retention time for transesterification, biodiesel recovery yield, lipase life time, and solvent loss (if used) (3) process design regarding water recycle and heat integration and (IV) by-product credit. It has been found that lipase cost contributes a great part of the total production cost. [Pg.190]

To account for the variation of the dynamics with pressure, the free volume is allowed to compress with P, but differently than the total compressibility of the material [22]. One consequent problem is that fitting data can lead to the unphysical result that the free volume is less compressible than the occupied volume [42]. The CG model has been modified with an additional parameter to describe t(P) [34,35] however, the resulting expression does not accurately fit data obtained at high pressure [41,43,44]. Beyond describing experimental results, the CG fit parameters yield free volumes that are inconsistent with the unoccupied volume deduced from cell models [41]. More generally, a free-volume approach to dynamics is at odds with the experimental result that relaxation in polymers is to a significant degree a thermally activated process [14,15,45]. [Pg.659]

However, coal reactivity as measured by total conversion to liquids and gases becomes less dependent on coal parameters as processing severity increases. The effect of process temperature in the hot-rod reactor was studied using three coals of varying properties. These were Waterberg, Sigma and Landau. At 650°C the conversion yields of these coals were 89, 90 and 88 per cent of the coal (dmmf) respectively. Within experimental error the conversion yields had converged to the same value, whereas at 500°C the conversion yields were 85, 75 and 65 per cent respectively. [Pg.52]

The PIIS has been calculated as a total score, which is the sum of a chemical score and a process score (Table 1). The chemical score consists of inventory, flammability, explosiveness and toxicity. The process score includes temperature, pressure and yield. Some of the scores are based on similar tables in the Dow and Mond Indices. Others have been constructed by dividing the domain of values of a parameter into ranges and assigning a score to each range. They are supposed to be modified in the future. [Pg.25]

The corrected parameters are used to calculate a new A matrix and F vector, new corrections are calculated and the process is repeated until the calculated corrections are essentially zero. As will be shown later, a total of four parameters must be specified in order to determine a unique solution for the E and C numbers, because we are not dealing with linear simultaneous equations. The following parameters were held fixed and not allowed to vary iodine Ea = 1.00 iodine Ca = 1.00 DMA Eb = T32 diethyl sulfide Cb=7.40. These latter two parameters where selected to yield a solution close to the earlier one 39). [Pg.92]

The basis and various parameters for the economic analysis are given in Table II. The overall column efficiency used was obtained from a plot of efficiency vs. the product of relative volatility and liquid viscosity (9), corrected to match predicted (10) data for the propane-propylene system. The value from the plot (9) was increased by a factor required to make the efficiency of the propane-propylene binary distillation equal to 100%. Costs were calculated by the Venture Analysis method (II), because this method yields the appropriate weighting factors for the fixed and operating costs in order to calculate the total costs. Results are expressed as annual costs, before taxes. The important process variables are discussed below. [Pg.33]


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See also in sourсe #XX -- [ Pg.46 , Pg.47 ]




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