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Production flow chart

Whereas the production flow charts of inorganic pigments appear to be simple, the actual processes can be very compHcated. Many pigments are not pure chemical compounds, but can be multiphase systems contaminated with various impurities and modifiers. Because pigments are fine powders, the physical properties are as critical to their appHcation performance as are the chemical properties. [Pg.6]

A plane schematic drawing of the thick film oxygen sensor is shown in Figure 3. The protective layer is eliminated. A part of each platinum lead wire is embedded in the alumina substrate. The earth line of the heater and sensor is common. Figure U shows a production flow chart for the thick film oxygen sensor. [Pg.102]

Figure J. Industrial production flow chart in Asian countries (ESCAP, 1995). Figure J. Industrial production flow chart in Asian countries (ESCAP, 1995).
Figure 4.17 Photos of a hollow fibre membrane module consisting of 129 bundles (889 fibres) propped up on a vacuum supply plate holder (a) and integrated in the system for oxygen production flow chart (b) and photo of the system (c). fSource Reproduced from Ref. [96], with permission from Elsevier)... Figure 4.17 Photos of a hollow fibre membrane module consisting of 129 bundles (889 fibres) propped up on a vacuum supply plate holder (a) and integrated in the system for oxygen production flow chart (b) and photo of the system (c). fSource Reproduced from Ref. [96], with permission from Elsevier)...
The first industrial hardboard was developed by W. Mason in the mid-1920s he found that a mat of wet fiber pressed in a hot press would produce a self-bonded flat panel with good strength, durabiUty, and stabiUty. The product was patented in 1928, trademarked as Masonite, and commercial production began. Over time several other processes for producing hardboards have been developed from modifications of the original process. Brief descriptions of these processes foUow and a flow chart of the process is shown in Figure 5. [Pg.386]

The performance of black powder is critically dependent on the degree of intimacy of the components in the product. The manufacture of black powder is essentially a procedure for bringing the ingredients into maximum mutual contact. A detailed flow chart for the conventional process is presented in Figure 10. [Pg.51]

Fig. 3. Flow chart for the sulfate process for production of the pigment titanium white. Fig. 3. Flow chart for the sulfate process for production of the pigment titanium white.
C to give the expected 2-methyl-1-butene in high selectivites (24). The AI2O2 catalyzed process can be optimized to give di- -pentyl ether as the exclusive product (23). Dehydration of 1-pentanol over an alkah metal promoted AI2O2 catalyst at 300—350°C provides 1-pentene at selectivities of 92% (29,30). Purification produces polymerization grade (99.9% purity) 1-pentene. A flow chart has been shown for a pilot-plant process (29). [Pg.372]

Seven of the tools of quahty have been summarized (43). The first tool is a flow chart, used to help understand the organizational flow of a procedure or process. A flow chart should be constmcted with the fiiU participation of the people who do the work. Its principal benefit is to enable teams, such as problem-solving or productivity improvement teams, to reach a common vision of the work flow. Its use enables the improvement effort to begin with this common understanding. Figure 3 contains an example for manufacture of a polymeric material. [Pg.369]

Fig. 1. Simplified flow chart for the production of metallic chromium and chromium compounds from chromite. Fig. 1. Simplified flow chart for the production of metallic chromium and chromium compounds from chromite.
As can be noted in Figure 21.7.2, steam and ediane are mi.xed before entering die reactor tubes where pyrolysis reacdons take place. All feed and product lines must be equipped with appropriate control devices to ensure safe operation. The FTA flow chart breaks down a TOP event (see descripdon of fault tree in Unit II) into all possible basic causes. Aldiough, diis mediod is more structured than a PHA, it addresses only one individual event at a dine. To use an FTA for a complete liazard analysis, all possible TOP events must be identified and investigated this would be extremely time consuming and perhaps urmecessary in a preliminary design. [Pg.629]

The complete production process of capacitor-grade powder includes the reduction of K2TaF7 that is usually diluted in molten KC1 and KF or some other molten alkali halide, followed by leaching, agglomeration and deoxidation of the product. Fig. 143 presents the flow chart of the process. [Pg.331]

Fig. 143. Flow chart for production of capacitor-grade tantalum powder. Fig. 143. Flow chart for production of capacitor-grade tantalum powder.
PLASTICS SIMPLIFIED FLOW CHART GUIDE FROM RAW MATERIALS TO PRODUCTS... [Pg.337]

Proof of payment, rights of reference letters, flow charts of production sites, manufacturing authorisations, CMP certificates, etc.)... [Pg.111]

Figure 1 shows a flow chart for part of a recursive modelling procedure, illustrated in this paper, which accepts as input a formula consisting of constituent raw material codes or formula names, and quantities. The procedure retrieves property data for each raw material in order to perform the required calculations. When the procedure encounters a constituent that is a formulated product, it calls itself using that product as input. The output of the procedure consists of the calculated properties of the formula, including those properties of the formula that would be retrieved from data files for non-formulated or purchased raw materials. By returning this latter set of properties, the procedure can treat formulas as raw materials. [Pg.55]

Figure 20-h Flow chart of pentose phosphate pathway and its connections with the pathway of glycolysis. The full pathway, as indicated, consists of three interconnected cycles in which glucose 6-phosphate is both substrate and end product. The reactions above the broken line are nonreversible, whereas all reactions under that line are freely reversible apart from that catalyzed by fructose-1,6-bisphosphatase. [Pg.164]

Understanding production process FMEA, Pareto analysis, flow charts [2]... [Pg.564]

Details of the specific types of apparatus need not normally be given except for nonstandard processes. A flow chart of the manufacturing operation and the in-process controls (and acceptance limits) is required. Proposals for alternative processes will need to be supported by appropriate data to show that the finished products resulting from these are consistent with the finished product specification. Certain manufacturing operations such as mixing may require additional information on quality parameters monitored during production and prior to batch release. Appropriate quality parameters should be included in the finished product specification regardless of the outcome of validation studies (e.g., content uniformity for solid and semi-solid products). [Pg.659]

Fig. 1 Flow chart of the production, use and waste disposal of cushion vinyl floor covering... Fig. 1 Flow chart of the production, use and waste disposal of cushion vinyl floor covering...
Figure 1. General flow chart for production of glandless cottonseed food ingredients. Figure 1. General flow chart for production of glandless cottonseed food ingredients.
Fig. 11. Flow chart of a typical pDNA production process. After fermentation cells are harvested and lysed by addition of alkaline solution. Clarification by filtration is followed by a series of chromatographic steps. After a final 0.22 pm filtration step the purified plasmid is aliquoted and stored... Fig. 11. Flow chart of a typical pDNA production process. After fermentation cells are harvested and lysed by addition of alkaline solution. Clarification by filtration is followed by a series of chromatographic steps. After a final 0.22 pm filtration step the purified plasmid is aliquoted and stored...
Fig. 1. An overview of the DCLD tier/triage flow chart Boxes 1, 2, and 3 are taken from the Office of Device Evaluation decision tree, which is routinely used to determine whether a product can be reviewed as a 510(k) and found substantially equivalent to a predicate (currently marked) device or whether the product must be handled as a fundamentally new product and submitted to a PMA review. Box 4 determines the novelty of the product in terms of analyte, matrix, and/or technology. If new issues of safety and effectiveness are raised, a highly novel product might require review as a PMA. If the issues of safety and effectiveness are not new but require high-level scrutiny, then a tier III review is warranted. Examples of products requiring a tier III review would include 1. Analyte troponin for diagnosis of MI (with creatinine kinase as the predicate) 2. Matrix sweat patches for drugs of abuse (with urine drugs of abuse tests as the predicate) and 3. Technology nucleic acid... Fig. 1. An overview of the DCLD tier/triage flow chart Boxes 1, 2, and 3 are taken from the Office of Device Evaluation decision tree, which is routinely used to determine whether a product can be reviewed as a 510(k) and found substantially equivalent to a predicate (currently marked) device or whether the product must be handled as a fundamentally new product and submitted to a PMA review. Box 4 determines the novelty of the product in terms of analyte, matrix, and/or technology. If new issues of safety and effectiveness are raised, a highly novel product might require review as a PMA. If the issues of safety and effectiveness are not new but require high-level scrutiny, then a tier III review is warranted. Examples of products requiring a tier III review would include 1. Analyte troponin for diagnosis of MI (with creatinine kinase as the predicate) 2. Matrix sweat patches for drugs of abuse (with urine drugs of abuse tests as the predicate) and 3. Technology nucleic acid...
Figure 19.8. Flow chart for design of production and preparative gas chromatographs(13). Feedback is shown by broken lines. A, B and C are principal calculation loops... Figure 19.8. Flow chart for design of production and preparative gas chromatographs(13). Feedback is shown by broken lines. A, B and C are principal calculation loops...
Figure 24.1 Flow chart of RACE-PCR protocol adopted with slight modifications from the instruction manual of the Marathon cDNA amplification kit. Poly A+ RNA is used for the generation of an adaptor-ligated cDNA library. Fragments containing the 5 - and the 3 -end of the cDNA coding for the carrier are amplified from the uncloned library with adaptor primers and gene-specific primers. Afterwards, a full-length clone is generated from the individual RACE products by subcloning or end-to-end PCR. Figure 24.1 Flow chart of RACE-PCR protocol adopted with slight modifications from the instruction manual of the Marathon cDNA amplification kit. Poly A+ RNA is used for the generation of an adaptor-ligated cDNA library. Fragments containing the 5 - and the 3 -end of the cDNA coding for the carrier are amplified from the uncloned library with adaptor primers and gene-specific primers. Afterwards, a full-length clone is generated from the individual RACE products by subcloning or end-to-end PCR.
Manufacturing Processes Flow charts for production steps, controls for contamination, removal of impurities, purification steps, in-process tests, and batch records... [Pg.245]

Fig. 2.5 Flow chart for the production bioethanol from cereal grain... Fig. 2.5 Flow chart for the production bioethanol from cereal grain...
A partial flow chart illustrates the particular features of the production of a PVC sheet as follows ... [Pg.558]

A schematic flow chart of the beneficiation options that are currently in practice is shown in Fig. 7. These processing schemes are primarily employed for the production of pozzolan, but other products may result, such as carbon fuel and mineral grade filler. The fly ash beneficiation option applicable to a specific site is dependent on many factors, but the primary consideration is whether the fly ash is wet or dry. Once ash has been wetted, flotation is the only practical beneficiation option. It may be technically feasible to use thermal processes on damp ash, but the amount of heat required will be significantly increased, thus decreasing the economic value... [Pg.255]


See other pages where Production flow chart is mentioned: [Pg.143]    [Pg.205]    [Pg.120]    [Pg.143]    [Pg.205]    [Pg.120]    [Pg.78]    [Pg.340]    [Pg.652]    [Pg.254]    [Pg.278]    [Pg.562]    [Pg.10]    [Pg.847]    [Pg.37]    [Pg.53]    [Pg.212]    [Pg.14]    [Pg.815]   
See also in sourсe #XX -- [ Pg.104 ]




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