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Production laboratory-scale plant

Due to short residence times inside the micromixer almost no heat was released there. In the residence time tube, temperatures up to 150 °C have been observed. In these experiments, we were able to show that it is possible to finish the first reaction step on the continuous microreactor laboratory-scale plant in less than 60 s. The same reaction step in the cooled batch vessel of the production plant took about 4 h. With these results, we came to the conclusion that it should be possible to realize the first exothermic step of the process in a microreactor. After finishing this step continuously in a closed system, the reaction solution could be transferred into the existing batch vessel and be heated there to finish the second reaction step. As the time for the first step is reduced from several hours to a few minutes for the same amount of product, it should be possible nearly to double the capacity just by installing a microreactor right before the existing batch vessel to mix the first two educts. [Pg.1268]

In the laboratory or process research section a laboratory procedure for a fine chemical is worked out. The resulting process description provides the necessary data for the determination of preliminary product specifications, the manufacture of semicommercial quantities in the pilot plant, the assessment of the ecological impact, an estimation of the manufacturing cost in an industrial-scale plant, and the vaHdation of the process and determination of raw material specifications. [Pg.436]

The ROTOBERTY internal recycle laboratory reactor was designed to produce experimental results that can be used for developing reaction kinetics and to test catalysts. These results are valid at the conditions of large-scale plant operations. Since internal flow rates contacting the catalyst are known, heat and mass transfer rates can be calculated between the catalyst and the recycling fluid. With these known, their influence on catalyst performance can be evaluated in the experiments as well as in production units. Operating conditions, some construction features, and performance characteristics are given next. [Pg.62]

This chapter deals with sodium a-olefinsulfonate (AOS) and with sodium internal olefmsulfonate (IOS). AOS is a well-established product and is being applied in many household and industrial formulations. IOS of a sufficiently high quality has only recently been made on laboratory scale and pilot plant scale and has not yet been applied in commercial formulations. AOS and IOS have not only good wetting and detergency properties, but also good tolerance toward water hardness ions, a combination not always observed for other anionic surfactants. [Pg.364]

The photovoltaics industry could expand rapidly if the efficiency of polycrystalline modules could be increased to 15 percent, if these modules could be built with assurance of reliability over a 10- to 20-year period, and if they could be manufactured for 100 or less per square meter. Solar energy research has been largely directed toward only one of these issues efficiency. All research aimed at reducing manufacturing costs has been done in industry and has been largely empirical. Almost no fundamental engineering research has been done on either the laboratory scale or the pilot plant scale for cost-effective processes for the production of photoconverters. [Pg.62]

The main role of pilot plant is in the scale-up of polymer formulations from laboratory to full scale production and the development of new processes and techniques, including trials of new equipment. The laboratory is normally where the chemistry of new products and processes is investigated and established. When scale-up is contemplated, the use of commercial quality materials will normally be investigated, test procedures established and certain processing tolerances examined. An experienced chemist can frequently learn much on the laboratory scale that will indicate likely scale-up behaviour, but it is always prudent to then go through the pilot stage before embarking on full scale production. [Pg.455]

Scahng up will probably continue to be a problem since large reactors carmot be as efficient as small laboratory reactors. However, it may be possible to make laboratory or pilot-plant reactors that are more similar to large-scale reactors, allowing more rebable validation of the simulations and process optimization. The time from laboratory-scale to full-scale production should be shortened from years to months. [Pg.354]

Special reactors are required to conduct biochemical reactions for the transformation and production of chemical and biological substances involving the use of biocatalysts (enzymes, immobilised enzymes, microorganisms, plant and animal cells). These bioreactors have to be designed so that the enzymes or living organisms can be used under defined, optimal conditions. The bioreactors which are mainly used on laboratory scale and industrially are roller bottles, shake flasks, stirred tanks and bubble columns (see Table 1). [Pg.41]

There is an additional point to be made about this type of processing. Many gas-phase processes are carried out in a continuous-flow manner on the macro scale, as industrial or laboratory-scale processes. Hence already the conventional processes resemble the flow sheets of micro-reactor processing, i.e. there is similarity between macro and micro processing. This is a fimdamental difference from most liquid-phase reactions that are performed typically batch-wise, e.g. using stirred glass vessels in the laboratory or stirred steel tanks in industrial pilot or production plants. [Pg.257]

The solution of these problems is based on a simple idea the developed laboratory-scale process is used for manufacturing of a chemical product by parallelization of many small units. Although promising great advantages over scale-up, this procedure, denoted numbering-up , is not trivial by far. It cannot be carried out in a simple way due to the tremendous technological effort necessary a chemical plant with hundreds or even thousands of small-scaled vessels, stirrers, heaters, pumps. [Pg.679]

Raw materials and auxiliary products used in a process as well as materials of construction for equipment items can be the eause of scale-up effects . Pure raw and auxiliary materials must be used in laboratory studies to eliminate the influence of impurities on the ehoice of the process route, catalyst selection, and search for satisfactory process conditions. However, pure chemicals are usually too expensive to use for manufacture on a commercial scale. It is common practice to use raw materials of technical grade in a full-scale plant. These materials contain impurities, which can act as catalysts or inhibitors. They can react with reactants or intermediates, thereby decreasing yields and selectivities of desired produets. Therefore, raw materials of technical grade, even from different suppliers must first be tested on laboratory scale. [Pg.213]

In conclusion, we have developed an efficient asymmetric synthesis of the selective estrogen receptor modulator 1. This process was scaled up in the pilot plant for the early steps in the synthetic route and in kilo laboratory scale for the later steps and finally 4 kg of the final product was made. The key process development and project support milestones are summarized below ... [Pg.157]

CSI began development of its own hydroxylamine production process through laboratory-scale experimentation in 1997. Development continued with the construction of a 10 gal pilot plant, which was operational in early 1998. In July 1998, CSI leased approximately 20,000 square feet in a multiple-tenant building and began to set up the production facility. [Pg.170]

A large-scale plant for the production of 100 tons a month was known to be in operation in Germany at the end of World War II. It was also prepared on a laboratory scale by Saunders and Stacey2 before German reports were available, by the novel reaction Et0 Et0... [Pg.104]

The objectives of this laboratory-scale test were to quantitatively assess the rate and determine the mechanism of transfer (diffusional versus electrochemical) of organics and their breakdown products across the membrane (AEA, 200lj). For the test, a small, laboratory-scale SILVER II plant was constructed at Aberdeen Test Center at Aberdeen Proving Ground, Maryland, to accomplish the following ... [Pg.71]

Sterile producfs for injection represent a particular challenge for the pharmaceutics development group. To prepare injectables, the pharmacists need not only sterile rooms in which to work at the laboratory, pilot plant, and production scales of operation, but they also require pyrogen-free wafer. Pyrogens are impurities, generally originating with... [Pg.403]

Sulfur Emissicms Sulfur present in a fuel is released as SO2, a known contributor to acid rain deposition. By adding limestone or dolomite to a fluidized bed, much of this can be captured as calcium sulfate, a dry nonhazardous solid. As limestone usually contains over 40 percent calcium, compared to only 20 percent in dolomite, it is the preferred sorbent, resulting in lower transportation costs for the raw mineral and the resulting ash product. Moreover, the high magnesium content of the dolomite makes the ash unsuitable for some building applications and so reduces its potential for utilization. Whatever sorbent is selected, for economic reasons it is usually from a source local to the FBC plant. If more than one sorbent is available, plant trials are needed to determine the one most suitable, as results from laboratory-scale reactivity assessments are unreliable. [Pg.30]

Chabot s work was done in a laboratory-scale batch reactor. Experiments at lab scale are a common hrst step in process analyzer work, since they allow technical feasibility to be demonstrated relatively quickly and inexpensively without having to interfere with production targets in a commercial-scale plant. In this work, moreover, one of the two business goals (improving process understanding) could be largely accomplished without going beyond lab-scale experimentation. [Pg.507]

Improvement of microbial strains for the overproduction of natural metabolites has been the hallmark of all commercial fermentation processes. Therefore, the aim of this chapter is to highlight several aspects of process improvement to yield natural products for industry at the laboratory, pilot plant and factory scales. [Pg.603]


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See also in sourсe #XX -- [ Pg.272 ]




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