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Main schemes

The different industrial processes of thb type differ as foUon SL [Pg.106]

These are the earliest, operating at 24. 10 Pa absolute, and around 180 to 190 in which the carbamate is decomposed at about 160 by simple flashing in two stages (1.7 and 0.2.10 Pa absolute). The ammonia and carbon dioxide recovered are sent to other units (nitric aci4 ammonium sulfate, ammonium nitrate etc.). [Pg.106]

This type of instaUation, which was industriafized by Ckemico ( ), CPI (Chemical Processes of Ohio Incj Vulcan, Inventa, Stamicarbon, Weatherly etc., was abandoned with the increase in unit manufacturing capacities, and the consequent need to hnd markets for the by-products. [Pg.106]

The effluent from the s iithesis reactor is flashed and sent to a column, in which the excess ammonia is separated, condensed and recycled as a liquid to the reactor. The [Pg.106]

Ammonium carbamate is decomposed by Oash in several stages (two to foui% Ammonia and carbon dioxide in excess or liberated can then be recycled to the reactor wbkb [Pg.107]


There are two main schemes proposed for sequestration of carbon dioxide. The first (referred to as a chemical absorption process), suitable for use at low pressures and temperatures, is usually adopted where the CO2 is to be removed from exhaust flue gases. The second (usually referred to as a physical absorption process), for use at higher pressures, is recommended for separation of the CO2 in syngas obtained from conversion of fuel. [Pg.136]

Two main schemes exist for the separation and purification of tantalum and niobium using liquid-liquid extraction. The first is based on the collective extraction of tantalum and niobium from an initial solution into an organic phase so as to separate them from impurities that remain in the aqueous media, the raffinate. The separation of tantalum and niobium is subsequently performed by fractional stripping into two different aqueous solutions. In this case, stripping of niobium is performed using relatively weak acids prior to the stripping of tantalum. Fig. 125 presents a flow chart of the process. [Pg.276]

This is not in the desired form. However, the scheme is so clear that we can apply the algorithm to it directly, making the necessary adjustments as we go. The main scheme is simply ... [Pg.265]

The labels stored in LABEL are used simply to point to the next statement to be executed while calls are stacked or unstacked. Since LABEL is always used as an actual parameter, its value is carried along when a new call is instituted or an old call is completed. On the other hand, TOP is never used as an actual parameter. When PUSH(u) is simulated, a new call is begun with u as the new value of the formal parameter and the old value is "left behind" in the previous procedure but is not destroyed. When v POP is finally simulated, this new value of TOP goes into v, the call is ended and the old procedure is reentered with the previous value of TOP still there. In simulating STOP, the value of label becomes permanently and the calls are unpeeled until the main scheme is reentered at 3. STOP and everything halts. ... [Pg.278]

Let PR be the class of recursion augmented schemes defined in Section D of Chapter VII. Constable and Gries define a slightly different class P R using an alternative method of parameter passing. A scheme in P R contains a main scheme and procedure definitions. In this case, a procedure definition Qp contains at the start, in addition to a statement of formal parameters and local variables, a statement EETURN(z) where z is a new variable, the output variable, which can also appear in the instructions and calls of Qp. A call has the form v F(Up,...,un). If procedure Qp has formal parameters Xp,...,x, and output variable z, then the scheme executes as if call v F(Up,..., un) were replaced by... [Pg.351]

Construct a recursion augmented scheme P without iteration (the main scheme and all procedure bodies are trees - no loops) and an interpretation I with domain the nonnegative integers and using only dyadic function,... [Pg.352]

Fig-1 The main scheme of AChE biotests technology (AChE - acetylcholinesterase PVA - polyvinil alcohol)... [Pg.149]

Principle Biosensors consist of paper matrixes and tissue enzyme preparations, often the pure enzyme AChE or AChE-containing cells. As seen in Fig.l, main scheme of the preparation technology and procedure includes (i) the preparation of same kinds of biotests-biosensors, which are paper matrixes impregnated with tissue preparation of AChE and covered by polymer film. (ii) biochemical reactions of the AChE activity with and without inhibitors tested and (iii) the photometric analysis of the samples for quantitative estimation of the biochemical reactions. [Pg.150]

As we ve already seen, program code is precise but tends to force you into too much detail. In design, you want to describe only the main scheme before proceeding to the detail. There are experimental wide-spectrum languages that cover both specification and coding but unfor-... [Pg.211]

The main schemes and experimental devices used for the detection of signals within this time range are briefly described below. In Section 3.7 we will also introduce the instrumentation used to measure optical signals in the picosecond-femtosecond range. [Pg.107]

The main schemes of the discharge (a) and transit time (b) methods are shown in Fig. 1. [Pg.7]

The main scheme is shown in Fig. 17. The photogenerated electron hole pairs transfer to the soliton-antisoliton pairs in 10 13s. Two kinks appeared in the polymer structure, which separates the degenerated regions. Due to the degeneration, two charged solitons may move without energy dissipation in the electric field and cause the photoconductivity. The size of the soliton was defined as 15 monomer links with the mass equal to the mass of the free electron. In the scheme in Fig. 17, the localized electron levels in the forbidden gap correspond to the free ( + ) and twice occupied ( — ) solitons. The theory shows the suppression of the interband transitions in the presence of the soliton. For cis-(CH)n the degeneration is absent, the soliton cannot be formed and photoconductivity practically does not exist. [Pg.30]

In contrast, EET has been historically modelled in terms of two main schemes the Forster transfer [15], a resonant dipole-dipole interaction, and the Dexter transfer [16], based on wavefunction overlap. The effects of the environment where early recognized by Forster in its unified theory of EET, where the Coulomb interaction between donor and acceptor transition dipoles is screened by the presence of the environment (represented as a dielectric) through a screening factor l/n2, where n is the solvent refractive index. This description is clearly an approximation of the global effects induced by a polarizable environment on EET. In fact, the presence of a dielectric environment not only screens the Coulomb interactions as formulated by Forster but also affects all the electronic properties of the interacting donor and acceptor [17],... [Pg.486]

Figure 3.1 indicates the main schemes that this evaluation gives rise to, in accordance with the products desired and the separation methods adopted. On the whole, indeed, the marirets for these products primarily guide the technological decisions. [Pg.197]

In the works cited the two main schemes of metamorphic transformation of siderite into magnetite at high temperatures were studied theoretically ... [Pg.215]

It is known [138,157] that the homogeneous catalytic hydrosilylation is characterized by two main schemes of the reaction proceeding ... [Pg.173]

SCHEME 2.2 Main scheme for oxygen electroreduction on platinum considering series and parallel pathways to water and hydrogen peroxide as products. [Pg.62]

Hydrogen cyanide is often obtained as a by-product of acrylonitrile manufacture (see Section 11.4). However, its availability by this method is steadily decreasing, in view of the improved yields of techniques for producing acrylonitrile and die faster growth of markets for methyl methacrylate. It is therefore produced by direct synthesis from hydrocarbons, according to three main schemes ... [Pg.204]

Thermal activation is generally divided into two thermally dependant steps, carbonization followed by activation. However, additional treatments are often applied. These are common industiial operations and are commented on below. The main scheme for activation production is shown in Fig. 8. [Pg.15]

Research and development in SPPS has conducted to two main schemes of protection, which are known as t-Boc/Bzl and Fmoc/tBu strategies (Chan and White 2000). In t-Boc/Bzl, the t-Boc (tert-butoxycarbonyl) group is used for the protection of the Na amino group and a benzyl or cyclohexyl for the side chains of several amino acids. In Fmoc/tBu, the Fmoc (9-fluorenyl methoxycarbonyl) group is used for the protection of the Na amino group and the tert-butyl group for the protection of the side chains of several amino acids (Albericio 2000). [Pg.254]

The designs of hardware system and type selection directly influence the overall performance of the system. This section details design principles of the hardware circuit, aiming at the need of function of the modular design. Touch screen with PLC is used as the main scheme, and it introduces the selection of the main function module, performance and advantages. [Pg.89]

The levels of were also investigated by Murray et al. With the exception of one weak y-ray (102 kev) which is of M 2 type and does not appear to be a part of the main scheme, all the remaining y-rays can be incorporated in three rotational families of odd parity, all apparently consistent with Nielson s scheme. As already pointed out the energies of this system show irregularities... [Pg.350]

In subsequent stages of the work a temporary jetty was provided to avoid the need for further risky beach launching. The required approvals and consents for construction of a temporaiy landing structure cannot be quickly secured. The need for such provision must therefore be considered at scheme design stage and the appropriate consents included with the main scheme. [Pg.119]

The effects of various reactor configurations on the properties of the polymer (MWD, CCD, etc.) have been reviewed for each of the three main schemes of polymerization kinetics. Reactor selection based on polymerization kinetics as well as practical considerations will now be discussed. Since polymers are products by process , it is not surprising that very specific conclusions can... [Pg.156]

The names of copolymers, derived either from the main scheme or the alternative, can be further modified to indicate various structural features. For example, the chemical nature of end groups can be specified as a-X-)-carboxy-6ZocA-copoly(st5n ene/butadiene). [Pg.5047]

Let us consider the trial harmonic solution, according to the main scheme of stability analysis... [Pg.29]


See other pages where Main schemes is mentioned: [Pg.221]    [Pg.221]    [Pg.251]    [Pg.277]    [Pg.272]    [Pg.286]    [Pg.27]    [Pg.106]    [Pg.97]    [Pg.471]    [Pg.35]    [Pg.29]    [Pg.27]    [Pg.106]    [Pg.417]    [Pg.178]    [Pg.630]    [Pg.1586]    [Pg.1588]    [Pg.124]   


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