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Process complexity

Xylenes. The main appHcation of xylene isomers, primarily p- and 0-xylenes, is in the manufacture of plasticizers and polyester fibers and resins. Demands for xylene isomers and other aromatics such as benzene have steadily been increasing over the last two decades. The major source of xylenes is the catalytic reforming of naphtha and the pyrolysis of naphtha and gas oils. A significant amount of toluene and Cg aromatics, which have lower petrochemical value, is also produced by these processes. More valuable p- or 0-xylene isomers can be manufactured from these low value aromatics in a process complex consisting of transalkylation, eg, the Tatoray process and Mobil s toluene disproportionation (M lDP) and selective toluene disproportionation (MSTDP) processes isomerization, eg, the UOP Isomar process (88) and Mobil s high temperature isomerization (MHTI), low pressure isomerization (MLPI), and vapor-phase isomerization (MVPI) processes (89) and xylene isomer separation, eg, the UOP Parex process (90). [Pg.52]

The fixed capital estimate depends on the definition of the plant. A grass-roots plant is a complete faciUty at a new location, including all utihties, services, storage faciUties, land, and improvements. If a process plant is located at an existing processing complex, it can usually share some of these auxihary faciUties. A battery-limits plant is defined as the process faciUty itself, so that the auxiUaries, off-site, and land-related items are excluded from the fixed capital estimation. However, a battery-limits plant maybe assigned allocated capital charges for the share of common utihty and service faciUties used by the plant. [Pg.442]

At processing complexes, central utiUties and other faciUties are shared by several battery-limits process plants. The capital cost of a central utiUty is sometimes charged to the capital cost of each battery-limits plant as an allocated capital cost based on the unit capital cost of the utiUty faciUty and the units of capacity of the utiUty required by the plant. In this case, the use charge per unit consumed only covers operating expenses. The alternative is to recover utihty capital costs, as well as operating expense, in the unit usage charge. [Pg.443]

The mixed refrigerant cwcle was developed to meet the need for hq-uefying large quantities of natural gas to minimize transportation costs of this fuel. This cycle resembles the classic cascade cycle in principle and may best be understood by referring to that cycle. In the latter, the natural gas stream after purification is cooled successively by vaporization of propane, ethylene, and methane. Each refrigerant may be vaporized at two or three pressure levels to increase the natural gas coohng efficiency, but at a cost of considerable increased process complexity. [Pg.1129]

The template methods have also been used for the synthesis of a number of substituted Ln di(naphthalocyanine) complexes, LnNc2 [82-88]. Apart from thermal fusion by conventional heating processes, complexation has been initiated by microwave radiation, although only a few publications are devoted to the template synthesis of lanthanide bis(phthalocyanine) complexes by this method [89, 90]. The use of microwave radiation (MW) reduces the reaction time from several hours to several minutes. Unsubstituted complexes LnPc2 (Ln = Tb, Dy, Lu) were prepared [90] by irradiation (650-700 W) of a mixture of phthalonitrile with an appropriate lanthanide salt for 6-10 min (yields >70%). [Pg.233]

The two-step nature of SPDP crosslinking provides control over the conjugation process. Complexes of defined composition can be constructed by adjusting the ratio of enzyme to secondary molecule in the reaction as well as the amount of SPDP used in the initial activation. The use of SPDP in conjugation applications is extensively cited in the literature, perhaps making it one of the more popular crosslinkers available. It is commonly used to form immunoto-xins, antibody-enzyme conjugates, and enzyme-labeled DNA probes. A standard activation and coupling procedure can be found in Chapter 5, Section 1.1. [Pg.968]

The primary purpose of LOPA is to determine whether there are sufficient layers of protection against a specific accident scenario. As illustrated in Figure 11-16, many types of protective layers are possible. Figure 11-16 does not include all possible layers of protection. A scenario may require one or many layers of protection, depending on the process complexity and potential severity of an accident. Note that for a given scenario only one layer must work successfully for the consequence to be prevented. Because no layer is perfectly effective, however, sufficient layers must be added to the process to reduce the risk to an acceptable level. [Pg.501]

Development of a new air separation plant, which greatly reduces cost and process complexity... [Pg.323]

This lack of access to understandable information combined with the lack of ability to process complex biotechnology information leads many... [Pg.117]

Since surfactants are commercially produced by means of large-scale chemical processes, complex mixtures of homologues and isomeric compounds, e.g. non-ionics of the alkylethoxylate type that may differ in length of alkyl as well as polyether chains, can result. The determination and differentiation of the products in quality control during production and trade is a somewhat easier task. However, more difficulties arise in the analysis of the compounds of these mixtures and formulations in environmental samples. [Pg.63]

Selectivity Process Complexity Commercial Status References... [Pg.19]

FA can interact with clay minerals and are known to form stable complexes with metal ions and hydrous oxides [59,61]. The operational technique for isolation of HA involves a pH-induced precipitation and it is likely that accessory minerals may be associated with the precipitation process. Complexes of HA and clay minerals are also formed, the increased ash content of HA suggesting that amorphous silica, iron hydroxides, and clay may aggregate with the HA fraction [58,60,61]. [Pg.123]

The processes that have been developed to accomplish gas purification vary from a simple once-through wash operation to complex multistep recycling systems. In many cases, the process complexities arise because of the need for recovery of the materials used to remove the contaminants or even recovery of the contaminants in the original, or altered, form (Kohl and Riesenfeld, 1979 Speight, 1993, and references cited therein). [Pg.238]

Ginisty H, Serin G, Ghisolfi-Nieto L, Roger B, Libante V, Amalric F, Bouvet P (2000) Interaction of Nucleolin with an Evolutionarily Conserved Pre-ribosomal RNA Sequence Is Required for the Assembly of the Primary Processing Complex. J Biol Chem 275 18845-18850 Ginisty H, Sicard H, Roger B, Bouvet P (1999) Structure and functions of nucleolin. J Cell Sci 112 761-772... [Pg.141]

To bridge this gap, liposomal transfection efficiency can be dramatically enhanced by the inclusion of peptides into the complex without increasing immunogenicity. Peptides can be selected to assist lipofection at each key stage of the process complex formation, cell targeting and uptake, endosomal disruption, and nuclear targeting. The purpose of this chapter is... [Pg.293]

In this chapter, the motivations to adopt MLR systems for optical e-beam, x-ray, and ion-beam lithographic systems will be given, followed by a survey of published MLR systems. Specific practical considerations such as planarization, pinhole and additive defects, interfacial layer, etch residue, film stress, interference effects, spectral transmission, inspection and resist stripping will be discussed. The MLR systems will be compared in terms of resolution, aspect ratio, sensitivity, process complexity and cost. [Pg.290]

To clarify the selection of a particular MLR system (ILR, 2LR, or 3LR system) a comparison in terms of process complexity, resolution, aspect ratio, linewidth tolerance, sensitivity and effort required for research and development will be given. Then a comparison between deep-UV and RIE PCM systems in terms of resolution, aspect ratio, substrate patterning processes allowed, temperature stability, resist removal at the alignment sites, tool-controlling parameters, and tool cost will be included. [Pg.342]


See other pages where Process complexity is mentioned: [Pg.132]    [Pg.161]    [Pg.270]    [Pg.443]    [Pg.1547]    [Pg.112]    [Pg.1182]    [Pg.86]    [Pg.321]    [Pg.217]    [Pg.807]    [Pg.55]    [Pg.205]    [Pg.55]    [Pg.13]    [Pg.69]    [Pg.263]    [Pg.273]    [Pg.28]    [Pg.265]    [Pg.21]    [Pg.135]    [Pg.112]    [Pg.68]    [Pg.208]    [Pg.304]    [Pg.342]    [Pg.343]    [Pg.344]    [Pg.344]    [Pg.89]    [Pg.330]   
See also in sourсe #XX -- [ Pg.321 ]




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Crystallization processes complexity

Cyanide complexes process

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Electron-transfer processes in macrobicyclic complexes

Electropolymerization—A Complex Process Oversimplified

Heterogeneous process complex nonlinear interaction

Host-guest complexation process

Hydride transfer processes from metal complexes

Insertion processes complexes

Interfacial processes complexation

Interfacial processes complexation agents, effect

Intermolecular complex electron transfer process

Intersystem-crossing processes complexes

Its Basic Chemistry and Advantages as a Metal Complexation Process

Leach process complex

Ligand site environment, influence complexation process

Ligolytic Processes - Simple vs. Complex

Macromolecular metal complexes structuring process

Mechanisms Complex-Induced Proximity Effect Process, Kinetically Enhanced Metalation, and Overriding Base Mechanism

Mixed solvent effect on processes of complex formation

More Complex Processes

Nitrosyl complexes oxidative processes

Nitrosyl complexes reductive processes

Non-Equilibrium Processes Are Usually Complex

Nuclear pore complex processing

Nucleophilic substitution process Meisenheimer complex

Olefin complexes Wacker process

Other Units and Complex Processes

Platinum complexes intramolecular processes

Process Complexities in Scale-up

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Ruthenium complex charge-transfer process

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Substitution Processes in Dimeric Metal Complexes

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