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Extraction process counter-current

Type D Extraction is from material which is sufficiently fluid to be pumped and the product is also a fluid. In this case extraction takes place in a high pressure column in which the material to be extracted flows counter-current to the solvent stream. Depending on the product, the separation takes place by release of pressure or by adsorption in standard pressure vessels or by absorption in a high pressure vessel operated as a column (Table 8.1 D). Examples of type D processes include the refining and fractionation of seed oils and the fractionation of milk fat at pilot plant scale. [Pg.234]

Pressure autoclaves (1-3.5 MPa) in batch or multistage batteries are in use to hydrolyze in cycles more or less continuously. In advanced processes, counter-current extraction technologies are applied to get a high degree of h. Many variations are in use, and complete process units are available. [Pg.142]

A beryUium concentrate is produced from the leach solution by the counter-current solvent extraction process (10). Kerosene [8008-20-6] containing di(2-ethylhexyl)phosphate [298-07-7] is the water-immiscible beryUium extractant. The slow extraction of beryUium at room temperature is accelerated by warming. The raffinate from the solvent extraction contains most of the aluminum and aU of the magnesium contained in the leach solution. [Pg.66]

Solids may be processed continuously or semicontinuously by pumping slurries or by using lock hoppers. An example is the separation of insoluble polymers by floatation with a variable-density SCF. For liquid feeds, multistage separation may be achieved by continuous counter-current extraction, much like conventional liquid-hquid extraction. The final produces may be recovered from the extract phase by a depressurization, a temperature change, or by conventional distillation. [Pg.2001]

In the extraction process, the LPG from the prewash tower enters the bottom of an extractor column. The extractor is a liquid/liquid contactor in which the LPG is counter-currently contacted by a caustic solution. Another option is the use of a fiber film contacting device. The mercaptans dissolve in the caustic (Equation 1-14). The treated LPG leaves the top of the extractor and goes on to a settler, where entrained caustic is separated. [Pg.37]

Multistage counter-current liquid-liquid extraction is a typical continuous process. Fig. 121 shows a schematic diagram of the process. The slope of the line depends on the volumetric ratio of the aqueous and organic phases. The aqueous and organic phases move through the system as two counter currents. The raffinate from a specific extraction stage moves on to the next stage, to be mixed with a relatively fresh portion of the extract, i.e. extractant that was previously mixed with a low-concentration aqueous solution. [Pg.272]

Fig. 122. General scheme of liquid-liquid extraction process using the multistage counter-current method. The three main steps are extraction, washing and stripping. Fig. 122. General scheme of liquid-liquid extraction process using the multistage counter-current method. The three main steps are extraction, washing and stripping.
Layered-type structure, 92-100 Lewis acidity, 15 Liquid - liquid extraction collective, 276-277 counter-current scheme, 272 equipment, 273 extractants, 279-281 mechanism, 274-276 multistage counter-current, 271 multistage cross-current, 270 one-stage process, 270 principals, 267-269 process performance, 282-283 process schemes, 277,278, selective, 277-278 with 2-octanol, 284-291... [Pg.385]

In addition, some plutonium is also lost to the salt as PuCl3. A two-step counter-current extraction is used to minimize the amount of salt used in the MSE process, reduce plutonium losses... [Pg.366]

Present production processes use two stage counter-current extraction to remove americium from molten plutonium with magnesium chloride based salts. Both 35 mole % NaCl - 35 mole % KC1 - 3D mole % MgCl2 and 50 mole % NaCl-26 mole % CaCl2 - 24 mole % Mg Cl 2 are used for americium extraction. Figures 4 and 5 show the ternary phase diagrams for these salt systemsU0). [Pg.386]

The basic process outline is depicted in Figure 5.2 moist un-roasted coffee beans and CO2 are fed counter-currently into the extractor under supercritical conditions. Caffeine is selectively extracted into the CO2 and this stream is led to a water-wash column to remove caffeine at a reduced pressure, the CO2 being recycled back to the extraction column. Extraction of the caffeine into water is necessary to avoid dropping the CO2 pressure too low, since compression is energy-intensive. There is now the problem of separating the caffeine (which is used in soft drinks and pharmaceu-... [Pg.138]

Salex A process for purifying sodium chloride. Continuous counter-current extraction with brine removes the impurities without dissolving the salt. There are three variants SALEX-B, SALEX-C, AND SALEX-M. Developed by Krebs Swiss. First operated in 1982. [Pg.233]

Van Ruymbeke (2) A process for dehydrating 95 percent aqueous ethanol by counter-current extraction of the vapor with glycerol. [Pg.282]

NN applications, perhaps more important, is process control. Processes that are poorly understood or ill defined can hardly be simulated by empirical methods. The problem of particular importance for this review is the use of NN in chemical engineering to model nonlinear steady-state solvent extraction processes in extraction columns [112] or in batteries of counter-current mixer-settlers [113]. It has been shown on the example of zirconium/ hafnium separation that the knowledge acquired by the network in the learning process may be used for accurate prediction of the response of dependent process variables to a change of the independent variables in the extraction plant. If implemented in the real process, the NN would alert the operator to deviations from the nominal values and would predict the expected value if no corrective action was taken. As a processing time of a trained NN is short, less than a second, the NN can be used as a real-time sensor [113]. [Pg.706]

The GS enriching process is a counter-current gas-liquid extraction done at a pressure of 2000 kPa in a sieve tray tower with the upper half operating at 30 C and the lower at 130 C. ( 5) In the top half of the tower, feedwater extracts deuterium from the upflowing cold H2S, reaching a maximum at the centre of the tower. The recycled lean H2S entering the lower hot half of the tower strips deuterium from the water, which then leaves the system depleted in deuterium. A cascade of several stages is used to reach the desired feed concentration for the final water distillation or finishing unit. Transfer between cascades can be either by gas or liquid from the centre of the tower. [Pg.324]

In the United States and most parts of the world, iodine is obtained com-merciaUy from brine wells. Many subsurface brines have iodine concentrations in the range of 10 to 100 mg/L. Various extraction processes are known including (i) precipitation with silver nitrate, (ii) oxidation with chlorine, and (hi) ion exchange. In the chlorine oxidation process, natural subsurface brine first is acidified with sulfuric acid and then treated with chlorine. Chlorine hberates iodine from the brine solution. Iodine is blown out into a counter-current stream of air. It is dissolved in a solution of hydriodic acid and sulfu-... [Pg.398]

Laboratory studies of the rearrangement process began with semi-continuous operation in a single, 200-mL, glass reactor, feeding 1 as a liquid and simultaneous distillation of 2,5-DHF, crotonaldehyde and unreacted 1. Catalyst recovery was performed as needed in a separatory funnel with n-octane as the extraction solvent. Further laboratory development was performed with one or more 1000-mL continuous reactors in series and catalyst recovery used a laboratory-scale, reciprocating-plate, counter-current, continuous extractor (Karr extractor). Final scale-up was to a semiworks plant (capacity ca. 4500 kg/day) using three, stainless steel, continuous stirred tank reactors (CSTR). [Pg.333]

The highly selective biocatalytic reactions afford a substantial reduction in waste. The overall isolated yield is greater than 90%, and the product is more than 98% chemically pure with an enantiomeric excess of >99.9%. All three evolved enzymes are highly active and are used at such low loadings that counter-current extraction can be used to minimize solvent volumes. Moreover, the butyl acetate solvent is recycled with an efficiency of 85%.The E factor (kgs waste per kg product) for the overall process is 5.8 if process water is excluded (2.3 for the reduction and 3.5 for the cyanation) [47]. If process water is included, the E factor for the whole process is 18 (6.6 for the reduction and 11.4 for the cyanation). The main contributors to the E factor are solvent losses which accounted for 51% of the waste, sodium gluconate (25%), NaCl and Na2SO4 (combined circa. 22%). The three enzymes and the NADP cofactor account for <1% of the waste. The main waste streams are aqueous and directly biodegradable. [Pg.17]

The principle Zr ore, zircon (Zr silicate) is processed by caustic fusion or by direct chlorination of milled coke and zircon mixts. Washing of the Na fusion cake leave an acid soluble hydrated Zr oxide, whereas chlorination yields mixed Si and Zr tetrachlorides which are separated by distillation. Removal of the Hf from the Zr takes place through counter current liq-liq extraction (Ref 33), For this purpose the oxide or the tetrachloride is dissolved in dil hydrochloric acid to which ammonium thiocyanate is added as a complexing agent. The organic extracting phase is methyl isobutylketone... [Pg.434]

The iron oxide used in the purification of coal gas gradually becomes richer in sulphur and can repeatedly be revivified by exposure to air until the sulphur amounts to about 40 per cent., of the whole the mixture is then of greater value as a source of sulphur. The spent oxide, as it is commonly termed, is frequently applied to the production of sulphur dioxide or sulphuric acid, but the extraction of its sulphur by carbon disulphide has been effected as a successful commercial process using the system of counter-currents the mass is exhausted of sulphur, whilst a saturated solution of sulphur is obtained, from which the solvent can be distilled and returned to the extraction process. [Pg.11]

Figure 2.7 illustrates the similarity between the counter-current extraction (CCE) process and the chromatographic process. [Pg.62]

The pulp recovered during screening may be transferred to a pulp-wash operation to yield further soluble solids by counter-current extraction with water. The washed pulp may be held for further processing or included with the bulk of ejected peel material from the extractors. This is milled, treated with lime (calcium hydroxide or calcium oxide) to break down pectin and reduce water retention, pressed, dried to c.10-12% moisture content and finally converted to pellets. Being high in carbohydrates these are used as filler in livestock feed blends. [Pg.51]

A flavouring essence is a traditional flavouring product prepared by washing a selected oil blend (predominately citrus oils) with an aqueous alcoholic solvent mixture (e.g. 60% ethanol/40% water). It is an extraction process in which the aqueous extract phase becomes the flavouring. The process is earned out under cool temperatures, for example, 5-10°C, either batch-wise or by counter-current extraction. The soluble oxygenated flavouring constituents present in the essential oil blend (e.g. citral in lemon oil) are effectively partitioned between the two phases of the mixture. The low temperatures employed ensure that the transfer of any oil into the hydro-alcoholic phase is minimised as a poorly processed essence will tend to cloud when used in the drink formulation. [Pg.108]

The Nippon Mining Co. refinery in Japan, which had previously used D2EHPA to extract cobalt from solutions obtained in the leaching of a mixed cobalt—nickel sulfide in sulfuric acid, changed in 1978 to the new extractant 2-ethylhexyl 2-ethylhexylphosphonate enabling a much-improved selectivity for cobalt over nickel to be obtained.8990 The process is carried out in three counter-current stages with an organic solution of phosphonic acid that has been converted to the ammonium salt by contact with aqueous ammonia ... [Pg.794]

Figure 32 A McCabe-Thiele diagram for a five-stage counter-current solvent extraction process... Figure 32 A McCabe-Thiele diagram for a five-stage counter-current solvent extraction process...

See other pages where Extraction process counter-current is mentioned: [Pg.417]    [Pg.125]    [Pg.546]    [Pg.1599]    [Pg.286]    [Pg.32]    [Pg.293]    [Pg.240]    [Pg.571]    [Pg.123]    [Pg.231]    [Pg.325]    [Pg.235]    [Pg.334]    [Pg.193]    [Pg.734]    [Pg.226]    [Pg.403]    [Pg.900]    [Pg.931]    [Pg.932]    [Pg.932]    [Pg.932]   
See also in sourсe #XX -- [ Pg.529 ]




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Counter-current processes

Current Process

Extraction process

Extractive processes

Processing extraction

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