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Problems with other reactions

Problems of Combining Resistances. Suppose that we have found the correct mechanism and resultant rate equation for the surface phenomenon. Combining this step with any of the other resistance steps, such as pore of film diffusion, becomes rather impractical. When this has to be done, it is best to replace the multiconstant rate equation by an equivalent first-order expression, which can then be combined with other reaction steps to yield an overall rate expression. [Pg.381]

Another consequence of increased reaction temperatures is the shift in the equilibrium concentrations of polyaromatic hydrocarbons and their hydrogenated derivatives. At high temperatures, the fully aromatic hydrocarbons are thermodynamically favored, especially at the pressures of today s HDS reactors. As the concentration of polyaromatics increases, the fluorescence of the finished fuel increases. This may cause problems with other specifications, as discussed shortly. [Pg.438]

The scope of the analysis aims to identify the process under consideration, in which plant it will take place, and with which chemicals it will be performed. The chemical reactions and unit operations must be clearly characterized. In this step, it is also important to check for interface problems with other plant units. As an example, when considering raw material delivery, it can be assumed that the correct raw material of the intended quantity and quality is delivered from a tank farm. Thus, it can be referred to the tank farm risk analysis, or the tank farm is to be included in the scope of the analysis. Similar considerations can be made for energy supply, to ensure that the appropriate energy is delivered. Nevertheless, loss of energy must be considered in the analysis, but it will be assumed that... [Pg.9]

We finish this chapter with some brief words about the mechanism of the addition of organometallics to carbonyl compounds. The problem with this reaction is that no-one really knows precisely what happens during the addition reaction. We know what the organic products are because we can isolate them and look at them using NMR and other spectroscopic techniques. But what happens to the metal atoms during the reaction ... [Pg.225]

A final point to be considered in the use of HPLC as an assay procedure is the enzyme itself. Will the activity be a pure enzyme Will it be part of a rather crude cell-free extract Or will it be present in a fermentation broth In the latter two cases, the presence of contaminating activities must be considered. While as mentioned above, these activities, by affecting the recovery of the product or even by affecting substrate levels during the course of the reaction, could easily cause problems with other assay procedures, they are not a problem for the HPLC assay method. Thus, HPLC should be considered first when activity in some crude extracts is to be assayed. [Pg.11]

The relatively mild conditions of this dimethyl sulfoxide activation method have been used to good effect to oxidize many sensitive substrates. For instance the alcohol (20 equation 10) was smoothly converted to the aldehyde without any racemization occurring, which can be a problem with other oxidizing systems. Similar advantages were noted in the oxidation of the alcohol (21), thus demonstrating the compatibili of some sensitive protecting groups to the reaction conditions. ... [Pg.297]

Samples that have very low target mRNA concentrations often display increased background, particularly if amplification above 35 cycles is required. The initial formation of these products can occur at low initial (ambient) temperatures, and are reduced or eliminated by the hot start approach, in which wax beads are added, melted to form a solid layer above the cDNA, and then the PCR master mix added on top. The two solutions are mixed and the PCR reaction begins after the thermocycler heats to 94°C. Background is sometimes due to the formation of primer dimers, a double-stranded PCR product consisting of the two primers and their complementary sequences. Sometimes these primer dimers contain extra sequences between the primers (14). When primer dimers form, they can be a major problem as they are very efficiently amplified and compete with amplification of the target cDNA. This is not a major problem with the primer sets described in Table 1, but can be a problem with other primer sets. With persistent problems, the hot start approach could be modified to add the cDNA, the primers, and the Taq polymerase separately. [Pg.78]

One problem with the reactions of C6H5N with organic carbonyl containing molecules was that the carbonyl group reactivity scale could not be extended past the simple esters HC02CH3 and CH3C02CH3 because their rates were already at the lower limit of determination in the FA. To get around this limitation, we examined other hypovalent species such as... [Pg.60]

Precautions Could cause allergic reaction to skin that comes in contact with latex. Sixteen deaths attributed to latex in 1990. Simple allergy results in skin welts, reddening and blistering as well as other respiratory problems. Severe problems with fatal reactions can occur from breathing problems and blood pressure drop. It can lead to anaphylaxis. Some believe the allergy is from the chemicals added in processing. [Pg.187]

The problem with mixers/reaction chambers is, that the down scaling of the fluidic process lead to Reynolds numbers which arc much smaller than the values that arc characteristic for the onset of turbulence [7]. Therefore it is not possible to increase the contact area of fluids to be mixed by "stirring". One is forced to look for solutions that increase the contact area in laminar flow situation. An elegant proposal for such a mixer/reaction chamber is fixjm Miyake et cd. [8], developed at our Institute. One of the fluids is pressed through a matrix of tiny holes perpendicular to the flow direction of the second fluid. The bulbs of the first fluid as they arise out of the holes into the second fluid leads to a large increase of the contact area and consequently of the diffusion process (see figure 7). As far as we know there are no other miniaturised mixers/reaction chambers described in the literature. [Pg.79]

If the reactor can be matched with other process streams (which is unlikely), then the reactor profile should be included in the heat integration problem. This would be a hot stream in the case of an exothermic reaction or a cold stream in the case of an endothermic reaction. [Pg.327]

Then N-Boc-O-benzylserine is coupled to the free amino group with DCC. This concludes one cycle (N° -deprotection, neutralization, coupling) in solid-phase synthesis. All three steps can be driven to very high total yields (< 99.5%) since excesses of Boc-amino acids and DCC (about fourfold) in CHjClj can be used and since side-reactions which lead to soluble products do not lower the yield of condensation product. One side-reaction in DCC-promoted condensations leads to N-acylated ureas. These products will remain in solution and not reaa with the polymer-bound amine. At the end of the reaction time, the polymer is filtered off and washed. The times consumed for 99% completion of condensation vary from 5 min for small amino acids to several hours for a bulky amino acid, e.g. Boc-Ile, with other bulky amino acids on a resin. A new cycle can begin without any workup problems (R.B. Merrifield, 1969 B.W. Erickson, 1976 M. Bodanszky, 1976). [Pg.232]

As with other problems with stoichiometry, it is the less abundant reactant that limits the product. Accordingly, we define the extent of reaction p to be the fraction of A groups that have reacted at any point. Since A and B groups... [Pg.309]

Tocotrienols differ from tocopherols by the presence of three isolated double bonds in the branched alkyl side chain. Oxidation of tocopherol leads to ring opening and the formation of tocoquinones that show an intense red color. This species is a significant contributor to color quaUty problems in oils that have been abused. Tocopherols function as natural antioxidants (qv). An important factor in their activity is their slow reaction rate with oxygen relative to combination with other free radicals (11). [Pg.124]


See other pages where Problems with other reactions is mentioned: [Pg.53]    [Pg.128]    [Pg.215]    [Pg.106]    [Pg.103]    [Pg.721]    [Pg.322]    [Pg.1977]    [Pg.8]    [Pg.82]    [Pg.128]    [Pg.138]    [Pg.1976]    [Pg.106]    [Pg.141]    [Pg.1053]    [Pg.148]    [Pg.283]    [Pg.151]    [Pg.316]    [Pg.15]    [Pg.208]    [Pg.142]    [Pg.156]    [Pg.159]    [Pg.318]    [Pg.125]    [Pg.284]    [Pg.22]    [Pg.456]    [Pg.508]    [Pg.392]   
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