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Productive phase

The production phase commences with the first commercial quantities of hydrocarbons ( first oil ) flowing through the wellhead. This marks the turning point from a cash flow point of view, since from now on cash is generated and can be used to pay back the prior investments, or may be made available for new projects. Minimising the time between the start of an exploration campaign and first oil is one of the most important goals in any new venture. [Pg.6]

A typical molecular dynamics simulation comprises an equflibration and a production phase. The former is necessary, as the name imphes, to ensure that the system is in equilibrium before data acquisition starts. It is useful to check the time evolution of several simulation parameters such as temperature (which is directly connected to the kinetic energy), potential energy, total energy, density (when periodic boundary conditions with constant pressure are apphed), and their root-mean-square deviations. Having these and other variables constant at the end of the equilibration phase is the prerequisite for the statistically meaningful sampling of data in the following production phase. [Pg.369]

Assuming that an equilibrium is now well established, the simulation may be restarted (not newly started) to begin with the sampling of structural and thermodynamic data. In our model case, data acquisition was performed for 3 ns (trajectory data plot not shown). For the production phase, also, the time evolution of the variables mentioned above should be monitored to detect stability problems or con-... [Pg.370]

Figure 7-16. Superimpasition of the X-ray structure of the tetracycline repressor class D dimer (dark, protein database entry 2TRT) with the calculated geometrical average of a 3 ns MD simulation (light trace). Only the protein backbone C trace Is shown, The secondary structure elements and the tertiary structure are almost perfectly reproduced and maintained throughout the whole production phase of the calculation,... Figure 7-16. Superimpasition of the X-ray structure of the tetracycline repressor class D dimer (dark, protein database entry 2TRT) with the calculated geometrical average of a 3 ns MD simulation (light trace). Only the protein backbone C trace Is shown, The secondary structure elements and the tertiary structure are almost perfectly reproduced and maintained throughout the whole production phase of the calculation,...
At the start of the production phase all counters are set to zero and the system is permitted t< evolve. In a microcanonical ensemble no velocity scaling is performed during the produc tion phase and so the temperature becomes a calculated property of the system. Varioui properties are routinely calculated and stored during the production phase for subsequen analysis and processing. Careful monitoring of these properties during the simulation car show whether the simulation is well behaved or not it may be necessary to restart i simulation if problems are encountered. It is also usual to store the positions, energie ... [Pg.383]

A thermodynamically stable system conserves energy. Thus, by monitoring the potential energy one can confirm that a stable (and productive) phase of the simulation has begun. Absence of systematic drift in computed averages is often used as a check on the stability of a Monte Carlo trajectory. Fluctuations in the energy... [Pg.98]

Electrochemical Fluorination. In the Simons electrochemical fluorination (ECF) process the organic reactant is dissolved in anhydrous hydrogen fluoride and fluorinated at the anode, usually nickel, of an electrochemical ceU. This process has been reviewed (6). Essentially all hydrogen atoms are substituted by fluorine atoms carbon—carbon multiple bonds are saturated. The product phase is heavier than the HF phase and insoluble in it and is recovered by phase separation. [Pg.298]

The alkene is allowed to react at low temperatures with a mixture of aqueous hydrogen peroxide, base, and a co-solvent to give a low conversion of the alkene (29). These conditions permit reaction of the water-insoluble alkene and minimise the subsequent ionic reactions of the epoxide product. Phase-transfer techniques have been employed (30). A variation of this scheme using a peroxycarbimic acid has been reported (31). [Pg.304]

Eig. 2. Cychc steam stimulation of an oil well (a) steam, injected into a well over a period of days or weeks in a heavy oil reservoir, introduces heat (huff) that, coupled with (b), alternate soak periods lasting a few days to allow (c) a production phase of weeks or months (puff), thins the oil. This process may... [Pg.190]

SBR mbber compounds are prepared in two stages the nonproductive and the productive phases. In the nonproductive phase the compound ingredients are mixed, usually in internal mixers (Banbury). The mixing time is usually short and the compound temperature is in the 160—195°C range. [Pg.499]

Using combustion to stimulate bitumen production is attractive for deep reservoirs and in contrast to steam injection usually involves no loss of heat. The duration of the combustion may be short (days) depending on requirements. In addition, backflow of oil through the hot 2one must be prevented or excessive coking occurs (15,16). Another variation of the combustion process involves use of a heat-up phase, then a blow-down (production) phase, followed by a displacement phase using a fire-water flood (COFCAW process). [Pg.357]

In the flux-growth method, crystals of the desired ceramic are precipitated from a melt containing the components of the product phase, often in addition to additives used to suppress the melting point of the flux. These additives remain in solution after crystal growth is complete. Crystals are precipitated onto seeds by slowly cooling the melt or the seed, or occasionally by evaporating volatile components of the melt such as alkaH haHdes, depressing the solubiHty of the product phase. [Pg.338]

The ongoing production phase involves the last two types, preamendment audits and periodic audits. The differences in docu-... [Pg.112]

It is clear that tire rate of growdr of a reaction product depends upon two principal characteristics. The first of these is the thermodynamic properties of the phases which are involved in the reaction since these determine the driving force for the reaction. The second is the transport properties such as atomic and electron diffusion, as well as thermal conduction, all of which determine the mobilities of particles during the reaction within the product phase. [Pg.253]

Are multidisciplinary teams employed to manage product realization and production phases ... [Pg.80]

Determine a methodology for design and development which integrates the major design tasks from the feasibility phase to the production phase. [Pg.276]

C) Preparation of Doxepin 1,530 grams of the product from step (B) is suspended in 4.5 liters dry tetrahydrofuran and 6.0 mols of butyl lithium in heptane is added during 1 hour. After an additional 30 minutes, 483 grams of 6,1 I dihydrodibenz-lb.eloxepin-ll-one, prepared as described in Belgian Patent 641,49B, is added to the deep red solution and the reaction was maintained at reflux for 10 hours. Water, 500 ml, is added at room temperature and the solvent is removed in vacuo. The crude residue is treated with 10% hydrochloric acid until acidic (pH 2) and then 1.5 liters benzene is added. After stirring, the mixture separates into 3 phases (an insoluble hydrochloride salt product phase, an aqueous phase and an organic phase). [Pg.539]

For a continuous SMB process, the specific identified amount or batch produced is defined by unit of time in such a way that ensures a homogeneous material and quality within specified limits. In the case of a continuous SMB production run a batch is defined by the amount produced in a fixed time interval. A time limitation during manufacturing using SMB is established by the same fixed time interval as the batch. The duration of the production phase is thus established, which does not affect the quality of the drug substance [66]. [Pg.277]

The major advantage of the use of two-phase catalysis is the easy separation of the catalyst and product phases. FFowever, the co-miscibility of the product and catalyst phases can be problematic. An example is given by the biphasic aqueous hydro-formylation of ethene to propanal. Firstly, the propanal formed contains water, which has to be removed by distillation. This is difficult, due to formation of azeotropic mixtures. Secondly, a significant proportion of the rhodium catalyst is extracted from the reactor with the products, which prevents its efficient recovery. Nevertheless, the reaction of ethene itself in the water-based Rh-TPPTS system is fast. It is the high solubility of water in the propanal that prevents the application of the aqueous biphasic process [5]. [Pg.259]

In comparison with classical processes involving thermal separation, biphasic techniques offer simplified process schemes and no thermal stress for the organometal-lic catalyst. The concept requires that the catalyst and the product phases separate rapidly, to achieve a practical approach to the recovery and recycling of the catalyst. Thanks to their tunable solubility characteristics, ionic liquids have proven to be good candidates for multiphasic techniques. They extend the applications of aqueous biphasic systems to a broader range of organic hydrophobic substrates and water-sensitive catalysts [48-50]. [Pg.278]

After field processing of wellhead products is complete, the oil and gas production phase of the industry passes into the refining stage, where the crude oil and field gas are further processed to make the products that ultimate users will purchase. The prices that refiners will pay determine the maximum allowable costs for oil and gas exploration and production. An oil or gas producer must be able to provide the product at a competitive price. For a vertically integrated oil company, no actual sale may take place, but the economics are much the same. [Pg.927]


See other pages where Productive phase is mentioned: [Pg.111]    [Pg.6]    [Pg.331]    [Pg.329]    [Pg.335]    [Pg.383]    [Pg.434]    [Pg.636]    [Pg.252]    [Pg.180]    [Pg.290]    [Pg.1668]    [Pg.2147]    [Pg.3]    [Pg.104]    [Pg.122]    [Pg.133]    [Pg.240]    [Pg.252]    [Pg.540]    [Pg.260]    [Pg.261]    [Pg.321]    [Pg.325]    [Pg.329]    [Pg.330]    [Pg.334]    [Pg.160]   
See also in sourсe #XX -- [ Pg.2 , Pg.39 , Pg.48 ]




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Acid hydrolysis products phase

Condensed-phase product

Condenser and Pressure Control—Single-Phase Product

Condenser and Pressure Control—Two-Phase Products

Drug product phase pure

Fission product metallic phases, irradiated

Fission product phases, irradiated fuel

Food products phase inversion

Gas-phase products

Homogeneous gas-phase production

Initial formation (nucleation) and growth of the product phase

Liquid phase major products

Mechanochemical product phases

Methanol, production liquid phase process

Natural products phase-transfer catalysis

Natural products solid phase syntheses

Natural products solid phase synthetic techniques

Natural products solid-phase extractions

No-interval coherently phased product

Nonaqueous phase liquid petroleum products

Oligosaccharide solid-phase synthesis products

Phase 1 Products Conceptualization (chapter

Phase inversion processes, production

Phase target product

Preservation products decomposition phases

Product Development Phases

Product phase recrystallization

Product phase space calculations

Product phases

Production Network Optimization Phase

Production phase

Production phase

RECENT ADVANCES IN SOLID-PHASE SYNTHESIS OF NATURAL PRODUCTS

Reversed-phase degradation products

Single-phase products

Solid-phase Target-Oriented Total Synthesis of Natural Products

Solid-phase organic synthesis natural products

Solid-phase synthesis side products

Testing product verification phase

Thermal decomposition solid-phase products

Three-phase Catalytic Reactors for Fine-chemicals Production

Water phase, radical production

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