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Pre steps

The production of (-R)-PAC by fermenting yeast was one of the first industrially applied biotransformations, which is used to nowadays to obtain (R)-PAC as a chiral pre-step for L-ephedrine 2 [6-9] (Scheme 1), and the optimization of the fermentation process is still a matter of research [10 23],... [Pg.18]

The composition of the solvent/electrolyte system may be adjusted. For EC-containing electrolytes, a cathodic pre-step is discussed for liquid electrolytes. [Pg.346]

Fig. 2.19 Stepped potential CO-stripping experiment, lOOmVs" in 1 M H2SO4, argon-purged solution. The sweep window was increased from 0.75V vs. NHE (continuous line) to 0.9V after the first two cycles (dashed line). The dotted line is the complete CV going directly to 0.9V without the pre-step at 0.75 V. Fig. 2.19 Stepped potential CO-stripping experiment, lOOmVs" in 1 M H2SO4, argon-purged solution. The sweep window was increased from 0.75V vs. NHE (continuous line) to 0.9V after the first two cycles (dashed line). The dotted line is the complete CV going directly to 0.9V without the pre-step at 0.75 V.
Molecular distillation process represents a type of vaporization at low pressure and low temperature. The transesterification can also be used as pre-step in molecular distillation process, like centrifuge distillatory. Batistella and Maciel studied the extraction in palm oil with 2,400 ppm of carotenoids applying a centrifugal distillator and a falling film distillator. The first process obtained a decomposition of 12 % at 155 °C and 25 % at 175 °C. The centrifugal distillator results in loss of 13 % at 190 °C and 14 % at 210 °C [83]. [Pg.4033]

For a few months, results obtained on a pre-industrial version of this new photothermal camera allow this technology to enter into the industrial step of its development. [Pg.398]

Stripping voltammetry involves the pre-concentration of the analyte species at the electrode surface prior to the voltannnetric scan. The pre-concentration step is carried out under fixed potential control for a predetennined time, where the species of interest is accumulated at the surface of the working electrode at a rate dependent on the applied potential. The detemiination step leads to a current peak, the height and area of which is proportional to the concentration of the accumulated species and hence to the concentration in the bulk solution. The stripping step can involve a variety of potential wavefomis, from linear-potential scan to differential pulse or square-wave scan. Different types of stripping voltaimnetries exist, all of which coimnonly use mercury electrodes (dropping mercury electrodes (DMEs) or mercury film electrodes) [7, 17]. [Pg.1932]

Anodic-stripping voltaimnetry (ASV) is used for the analysis of cations in solution, particularly to detemiine trace heavy metals. It involves pre-concentrating the metals at the electrode surface by reducmg the dissolved metal species in the sample to the zero oxidation state, where they tend to fomi amalgams with Hg. Subsequently, the potential is swept anodically resulting in the dissolution of tire metal species back into solution at their respective fomial potential values. The detemiination step often utilizes a square-wave scan (SWASV), since it increases the rapidity of tlie analysis, avoiding interference from oxygen in solution, and improves the sensitivity. This teclmique has been shown to enable the simultaneous detemiination of four to six trace metals at concentrations down to fractional parts per billion and has found widespread use in seawater analysis. [Pg.1932]

Improved sensitivities can be attained by the use of longer collection times, more efficient mass transport or pulsed wavefomis to eliminate charging currents from the small faradic currents. Major problems with these methods are the toxicity of mercury, which makes the analysis less attractive from an eiivironmental point of view, and surface fouling, which coimnonly occurs during the analysis of a complex solution matrix. Several methods have been reported for the improvement of the pre-concentration step [17,18]. The latter is, in fact. [Pg.1932]

The zeroth-order rates of nitration depend on a process, the heterolysis of nitric acid, which, whatever its details, must generate ions from neutral molecules. Such a process will be accelerated by an increase in the polarity of the medium such as would be produced by an increase in the concentration of nitric acid. In the case of nitration in carbon tetrachloride, where the concentration of nitric acid used was very much smaller than in the other solvents (table 3.1), the zeroth-order rate of nitration depended on the concentrationof nitric acid approximately to the fifth power. It is argued therefore that five molecules of nitric acid are associated with a pre-equilibrium step or are present in the transition state. Since nitric acid is evidently not much associated in carbon tetrachloride a scheme for nitronium ion formation might be as follows ... [Pg.38]

The introduction to Section 26 8 pointed out that mevalonic acid is the biosynthetic pre cursor of isopentenyl pyrophosphate The early steps m the biosynthesis of mevalonate from three molecules of acetic acid are analogous to those m fatty acid biosynthesis (Sec tion 26 3) except that they do not involve acyl earner protein Thus the reaction of acetyl coenzyme A with malonyl coenzyme A yields a molecule of acetoacetyl coenzyme A... [Pg.1091]

A method for calculating the dimensions of the cavities and narrow necks from the intrusion-extrusion curves has been proposed by Reverberi." " The method is essentially as follows the ascending curve (penetration) branch is measured in the usual way, but the descending curve is mapped out from a series of steps each step commences at the same maximum pressure, proceeds to a pre-determined minimum pressure which is different for... [Pg.184]

The overall requirement is 1.0—2.0 s for low energy waste compared to typical design standards of 2.0 s for RCRA ha2ardous waste units. The most important, ie, rate limiting steps are droplet evaporation and chemical reaction. The calculated time requirements for these steps are only approximations and subject to error. For example, formation of a skin on the evaporating droplet may inhibit evaporation compared to the theory, whereas secondary atomization may accelerate it. Errors in estimates of the activation energy can significantly alter the chemical reaction rate constant, and the pre-exponential factor from equation 36 is only approximate. Also, interactions with free-radical species may accelerate the rate of chemical reaction over that estimated solely as a result of thermal excitation therefore, measurements of the time requirements are desirable. [Pg.56]

Fig. 10. Flow diagram for the setup of a desalination plant employing reverse osmosis, including pre- and post-treatment steps. Fig. 10. Flow diagram for the setup of a desalination plant employing reverse osmosis, including pre- and post-treatment steps.
Pre-liming. Lime slurry, 0.25% lime on juice (0.250 g of CaO/100 g juice), is added to bring the pH of the mixture into the alkaline range. Insoluble calcium salts are precipitated as finely dispersed coUoids. Calcium carbonate in the form of recycled first carbonation sludge is added to provide coUoid absorption and stabilization. Temperature may be cool (50°C) or hot (80°C) depending on the temperature of the next step, or occasionally on the type of diffusion equipment. Retention time is 15 to 30 min. [Pg.26]

Although the precise mechanism of plasminogen activation is unknown, three principal theories have developed based on studies of the in vitro activation of native human plasminogen. Activation of native Glu-plasminogen in the absence of any plasmin inhibitor yields Lys —plasmin plus the so-called pre-activation peptides (PAP) formed by cleavage at LySg2 S E3 Activation takes place by a two-step mechanism in... [Pg.179]

Metal Cleaning. Citric acid, partially neutralized to - pH 3.5 with ammonia or triethanolamine, is used to clean metal oxides from the water side of steam boilers and nuclear reactors with a two-step single fill operation (104—122). The resulting surface is clean and passivated. This process has a low corrosion rate and is used for both pre-operational mill scale removal and operational cleaning to restore heat-transfer efficiency. [Pg.185]

Process development on fluidized-bed pyrolysis was also carried out by the ConsoHdation Coal Co., culminating in operation of a 32 t/d pilot plant (35). The CONSOL pyrolysis process incorporated a novel stirred carbonizer as the pyrolysis reactor, which made operation of the system feasible even using strongly agglomerating eastern U.S. biturninous coals. This allowed the process to bypass the normal pre-oxidation step that is often used with caking coals, and resulted in a nearly 50% increase in tar yield. Use of a sweep gas to rapidly remove volatiles from the pyrolysis reactor gave overall tar yields of nearly 25% for a coal that had Eischer assay tar yields of only 15%. [Pg.287]

Chemical exchange between hydrogen and steam (catalyzed by nickel—chromia, platinum, or supported nickel catalysts) has served as a pre-enrichment step in an electrolytic separation plant (10,70). If the exchange could be operated as a dual-temperature process, it very likely... [Pg.7]

Catalysts for dielectric surfaces are more complex than the simple salts used on metals. The original catalysts were separate solutions of acidic staimous chloride [7772-99-8J, used to wet the surface and deposit an adherent reducing agent, and acidic palladium chloride [7647-10-17, which was reduced to metallic palladium by the tin. This two-step catalyst system is now essentially obsolete. One-step catalysts consist of a stabilized, pre-reacted solution of the palladium and staimous chlorides. The one-step catalyst is more stable, more active, and more economical than the two-step catalyst (21,23). A separate acceleration or activation solution removes loose palladium and excess tin before the catalyzed part is placed in the electroless bath, prolonging bath life and stability. [Pg.107]

The project review process involves multiple steps that should be definea in management gmdelines (CCPS, 1993, pp. 57-61). The steps include (1) review pohcy, (2) review scheduling, (3) reviewtech-nique, (4) review team representation, (5) review documentation, (6) review follow-up, (7) review follow-up verification, and (8) review procedures change management. These steps define how a review, whether it be a safety review, environmental review, pre-start-up review, or whatever, is conducted and how closure of review aclion items is achieved. [Pg.2285]

The proeedure provides pre-eoneentration and separation 238,239,24op Am and Cm by anion exehanger eolumn AV-17 in NO - form and eation exehanger eolumn KU-2-8 in NH -form, Pu, Am, and Cm elutriated step-by-step by 2-hydroxy-Ao-butyrie aeid with pH 4,75. The sepai ation of Am -I- Cm and rai e eailh elements is eanied out on a eation exehanger eolumn KU-2-8 in H+-form by strip saturated HCl eontaining 20 % C,H OH. [Pg.279]

The flowchart on the next page shows an overview of steps for the pre-startup and startup phases of a typical tolling process. [Pg.81]

The question to answer for this pre-startup task is Who needs training for this process and to what level of detail One method to analyze training needs is offered by the Instructional Systems Design (ISD) technical training model. It points to the job task analysis method mentioned previously (Appendix D, ISD Model and Job Task Analysis Techniques) to identify procedure titles as a first step for determining which job positions require specific knowledge and skills. [Pg.94]


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See also in sourсe #XX -- [ Pg.67 ]




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Pre Rate-Determining Steps

Pre-concentration step

Step 1 Pre-qualification

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