Simultaneous Operations

Drum Separators Very coarse solids, up to 0.3 m (12 in), are often processed in a drum separator of the type shown in Fig. 19-32. This is similar to a ball-mill shell with hfters permanently attached to the wall. Medium and feed enter at one end, and the float product flows out through the discharge trunnion, while the sink is lifted by the rotation of the drum to a stationaiy launder, through which it is flushed out. Modifications of this type include division of the shell into two compartments, which permits simultaneous operation at two different piup densities resulting in various grades of products. The two-compartment revolving drum is illustrated in Fig. 19-32. 

Multiple batches operated simultaneously. Operator observes information about process from wrong display. Misoperation leading to undesired incident. 

In the desorption step, ammonia is passed downflow through the bed which has completed the adsorption cycle. The ammonia is heated to approximately the same temperature as that of the feed in the adsorption step in order to maintain a nominally isothermal operation. The first portion of the desorbate, although rich in n-paraffms, contains impurities and is recycled to the second bed which is simultaneously operating on the adsorption cycle. The remaining product is condensed and separated from ammonia. The product is freed of dissolved ammonia by distillation. 

In the case of lithium fluoride the ratio R i /Rj>- is 0.44. In this crystal there is double repulsion the repulsive forces between anion and anion and those between anion and cation are simultaneously operative. The inter-atomic distances are determined neither by the sum of the radii for the anion and cation nor by the radius of the anion alone, but are larger than those calculated by either method. Thus the lithium-fluoride distance is 0.05 A. (2.5%) larger than the sum of the radii, and one-half the fluorine-fluorine distance is 0.06 A. larger than the fluoride radius. 

Soil genesis is the result of four fundamental types of processes simultaneously operating at any part of the Earth s surface. As a soil develops, matter and energy enter the soil, can be transformed or translocated, and can leave the soil. The nature and magnitude of inputs, outputs, transformations, and translocations can vary widely from one site to another and result in numerous different types of soils. 

Some reactions of a given substrate under a given set of conditions display all the characteristics of Sn2 mechanisms other reactions seem to proceed by SnI mechanisms, but cases are found that cannot be characterized so easily. There seems to be something in between, a mechanistic borderline region. At least two broad theories have been devised to explain these phenomena. One theory holds that intermediate behavior is caused by a mechanism that is neither pure Sn I nor pure Sn2, but some in-between type. According to the second theory, there is no intermediate mechanism at all, and borderline behavior is caused by simultaneous operation, in the same flask, of both the SnI and Sn2 mechanisms that is, some molecules react by the SnI, while others react by the Sn2 mechanism. 

Availability constraints the macroscopic limits on material resources and the availability or up-time of equipment. Availability of raw materials is an obvious constraint at scheduling. Obviously, no catalytic hydrogenation can be done if the catalyst is unavailable. Simultaneous operation of certain tasks is restricted by the limited availability of common utilities such as steam, electricity, or labour. The priority sequence in a product chain needs to be respected by ensuring that intermediate products are manufactured in time to be available when required by a batch of the consecutive product. 

Closer examination of the mechanism for the Rh catalyzed carbonylation of ethylene provides a rationale for the poor selectivity. The mechanism for the carbonylation of ethylene (Scheme 37.1) is well known (6) and proceeds via two simultaneously operating mechanisms which generate a common EtRh(CO)2l2 intermediate which rapidly reacts with iodide (Eqn. 10) to generate EtRh(CO)2l3 . The first, and predominant, mechanism is a hydride mechanism (Eqns. 6-8 below) in which the proton required for the formation of HRh(CO)2l2 and initiation of the... 

The equations of motion of charged particles are output at simultaneous operation of electrical and thermoelectric fields with distributed potentials, and analytical solutions of them are obtained. Essentially variations of a trajectory of charged particles motion under operation of an additional thermoelectric field with a distributed potential are detected. This one can be used to create a new type of measuring instruments and functional converters. 

For non-simultaneously operating multi-sources it is necessary to check whether the data quality achieved is sufficient, especially for fast LC systems with very narrow peaks. A switching source splits the available acquisition time for the offered ionization types and therefore reduces the true acquisition rate of the mass spectrometer. However, simultaneously operating sources do not explicitly show which compound ionized with what technique. If this information is really necessary, two separate runs must be performed. 

When these latent conditions create an unfolding situation, the safety barriers present in an organization can be seriously affected. Svenson (Svenson, 2001) identifies three functional categories of safety barriers, e.g. technical, human, organizational. These safety barriers can be activated by different safety barrier systems, such as the closure of a valve automatically by a computer or manually by an operator. Moreover, a safety barrier system can (simultaneously) operate more than one safety barrier, like an operator who can close a valve, connect a hose, or a computer which closes down a machine and alerts an operator, etc. 

The second stage of the research cycle is the measurement stage. This is probably the most difficult stage because a successful experiment involves the simultaneous operation of many different types of measurement and control equipment. The failure of just one part negates the results of the entire experiment. The probability of this happening is quite high because a malfunction in the apparatus can re-occur or new malfunctions can appear. In some cases, these malfunctions can go undetected until an examination of the results shows that they are entirely inconsistent with predicted data. 

The effectiveness of the internal O2 transport by diffusion or convection depends on the physical resistance to movement and on the O2 demand. The physical resistance is a function of the cross-sectional area for transport, the tortuosity of the pore space, and the path length. The O2 demand is a function of rates of respiration in root tissues and rates of loss of O2 to the soil where it is consumed in chemical and microbial reactions. The O2 budget of the root therefore depends on the simultaneous operation of several linked processes and these have been analysed by mathematical modelling (reviewed by Armstrong... 

Some ROPs proceed with the simultaneous operation of two different mechanisms, for example, NCA copolymerizations initiated by some secondary amines proceed with both the amine and activated monomer mechanisms. The monomer reactivity ratios for any comonomer pair are unlikely to be the same for the two different propagations. Any experimentally determined r values are each composites of two different r values. 

It should be self-evident that the time dependencies of the fluorescent emissions may well be very complicated, because they must reflect the simultaneous operation of a large number of relaxation mechanisms. A complete understanding of the transient luminescent emissions must therefore involve an intimate knowledge of a large number of factors. 

At each of the three points where glycolytic reactions are bypassed by alternative, gluconeogenic reactions, simultaneous operation of both pathways would consume ATP without accomplishing any chemical or biological work. For example, PFK-1 and FBPase-1 catalyze opposing reactions ... 

Direct elimination of H2S and NH3 between NH4+ and WS42" can give WS3 chains, while an intramolecular redox reaction will produce HjS, NH3, S and WS2 layers. Scheme 1. Outlines the two slightly different pathways that may be simultaneously operative to deposit both WS3 and WS2 to form inorganic walls. 

For the actinoid complexes the approximation that the ligand field splittings are small compared with the spin-orbit coupling splittings of the free-ion terms is probably not very good. A proper treatment would involve the simultaneous operation by HER, HEF and HIS on the/ configurations. 

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