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Condensation stage

The Thomas algorithm begins by a for ward elimination, row by row starting down from the top row (j=l, the condenser stage), to give the following replacements shown in Fig. 13-50Z . For row T. [Pg.1283]

The final phase of resole manufacture is known as the condensation stage (Scheme 3). This is the actual process by which molecular weight is developed and involves the combination of the hydroxymethyl phenol intermediates to form oligomers. It can be reasonably well separated from the resole methylolation reaction in practice by maintaining reaction temperatures below about 70°C. The activation energy for condensation is higher than that for methylolation. This is not to say that condensation does not occur at temperatures below 70°C. It simply means that the methylolation is much faster than condensation at this temperature. [Pg.886]

CLC consists of two fluidised bed reactors, namely reducer and oxidiser. In the reducer reactor, fuel is fed along with the metal oxide containing oxygen, which is transferred from the metal oxide to the reactor as the combustion occurs (Figure 7). A flue gas containing over 99%v/v of C02 can be obtained by a simply condensation stage because of the fact that the exhaust gas at the reducer outlet is primarily formed by C02 and water vapour. This stream is then sent to further compression and permanent storage. [Pg.88]

The theoretical maximum yield from an entrainer sublimation process is the difference between the calculated sublimation rates corresponding to the conditions in the vaporisation and condensation stages. [Pg.882]

The problems associated with the mechanism of condensation were considered in [14, 70, 99, 102, 103]. From a theoretical viewpoint, there are three possible ways for the diazepine cycle to form and they differ in the sequence of the condensation stages (Scheme 4.30, reactions a-c). No unambiguous... [Pg.162]

Product recovery and capture can be carried out in a series of condensation stages, at different temperatures, in order to achieve different fractions enriched in target compounds. The temperature of each condenser has to be adjusted according to the downstream pressure in the circuit and the character of the compounds to be separated and recovered [37, 38]. Capture of the target-permeating compounds by condensation remains one of the main problems for competitive use of pervapora-tion systems, due to the energy costs involved to keep an adequate downstream pressure and to cool down the permeating stream. [Pg.252]

If the relative loads are reversed and the LPS availability exceeds the demand for LPS, this will cause the pressure in the LPS header to rise and the PC to reduce the bypass flow. When this let-down flow drops below the set point of FC-1, the previously inactive (saturated) FC-2 becomes active and admits that part of the LP steam which is not needed in the LPS header into the second condensing stage of the turbine. Any number of such bypass flow controllers can be used to sequentially respond to changes in the relative sizes of the work and LP steam loads. These controllers should be provided by integral action only, so that they will be saturated (and their control valves closed) until their set points are reached. [Pg.320]

Mathad et al.47 recently disclosed preparation of 3 following a similar process to the discovery route with only modifications at the condensation stage (Scheme 3). They achieved aldol condensation of 25 and 26 using sodium hydroxide as a base under phase transfer conditions to provide the intermediate 27 in excellent yield (88%). Overall yield of this route was 37%, an improvement over the original route. [Pg.259]

Quinacridone pigments are manufactured by either the condensation of 2,5-diarylamino-terephthalic acid or the oxidation of dihydroquinacridones followed by subsequent conditioning to produce the product in a pigmentary form of colloidal dimensions. For example, in the first process, the use of 2,5-dianilinoterephthalic acid results in the formation of trans linear quinacridone, PV 19, by a simple ring closure condensation where water is evolved as a by-product. Substitution of the aniline used to produce the diarylaminoterephthalic acid will result in pigments such as PR 122 where ditoluidinoterephthalic acid is used at the condensation stage. [Pg.108]

Time. An age determination based on extinct 16 Myr gave an age difference of only 0.2 + 0.2 Myr for magnetites from a Cl and a C2 chondrite (Lewis and Anders, 1975), suggesting that the entire condensation stage of the solar nebula was of that order. However, it now appears that ages reflect some combination of true age differences and variations in the initial ratio (Podosek,... [Pg.4]

When the makeup gas contains water or carbon dioxide, advantage is taken of the fact that these materials are absorbed completely by condensing ammonia. This requires the condensation stage to be located partially or wholly between the makeup gas supply point and the converter. This arrangement has the disadvantage that the... [Pg.145]

For splitting, 100 g of 1,1-dimethoxy diphenyl propane from the condensation stage (a) were heated to 200° C. in a distillation apparatus fitted with a Claisen attachment, followed by the addition of 0.5 g of concentrated phosphoric acid. The products formed during the splitting reaction distilled off over a period of 15 minutes at about 5 to 30 Torn According to analysis by gas chromatography, the distillate (95.5 g) contained 32.7 g of unsplit 1,1-dimethoxy diphenyl propane, 24.1 g of ira .9-p-anethole, 9.1 g of trans-o- and cns-p-anethole and 1.2 g of p-propyl anisole, corresponding to a yield of 91.4% of anetholes, based on reacted condensate. [Pg.100]

A two-stage distillation column consists of a partial condenser, stage 1, and a partial reboiler, stage 2, with no trays in between. A 100 mol/s stream consisting of a binary equimolar mixture of components 1 and 2 is fed to the reboiler. It is required to obtain online compositions of the distillate and the bottoms for control purposes. Online analyzers are not available, but the flow rates of the distillate and reflux rates can be measured in real time. The X-values of the lighter component, component 1, and the measured distillate rate, V, and reflux rate, Lj, are as follows ... [Pg.163]

Predicted column profiles for temperature, total vapor and liquid flow rates, and component vapor and liquid mole fractions are shown in Figure 6.24, where stages are numbered from the top down (stage 1 is the partial condenser, stage 14 is the partial reboiler). Computed heat exchanger duties are as follows ... [Pg.391]

Feed to stage 6 (stage 1 is the condenser stage 12 is the reboiler) Properties ... [Pg.394]


See other pages where Condensation stage is mentioned: [Pg.496]    [Pg.204]    [Pg.509]    [Pg.142]    [Pg.324]    [Pg.249]    [Pg.878]    [Pg.883]    [Pg.158]    [Pg.402]    [Pg.434]    [Pg.23]    [Pg.99]    [Pg.164]    [Pg.62]    [Pg.84]    [Pg.204]    [Pg.509]    [Pg.279]    [Pg.402]    [Pg.238]    [Pg.261]    [Pg.59]    [Pg.150]    [Pg.209]    [Pg.168]    [Pg.107]    [Pg.597]    [Pg.351]    [Pg.281]    [Pg.586]    [Pg.189]    [Pg.160]    [Pg.208]   


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