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Functional multifunctional

In addition, a reactor may perform a function other than reaction alone. Multifunctional reactors may provide both reaction and mass transfer (e.g., reactive distillation, reactive crystallization, reactive membranes, etc.), or reaction and heat transfer. This coupling of functions within the reactor inevitably leads to additional operating constraints on one or the other function. Multifunctional reactors are often discussed in the context of process intensification. The primary driver for multifunctional reactors is functional synergy and equipment cost savings. [Pg.7]

For a fixed extent of reaction, the presence of multifunctional monomers in an equimolar mixture of reactive groups increases the degree of polymerization. Conversely, for the same mixture a lesser extent of reaction is needed to reach a specified with multifunctional reactants than without them. Remember that this entire approach is developed for the case of stoichiometric balance. If the numbers of functional groups are unequal, this effect works in opposition to the multifunctional groups. [Pg.322]

The detailed analysis, involving many respondents inside and outside the company, led to changes in the overall innovation process, ie, a company-wide priority system for innovation projects, measures of innovation for each functional and business area, training and supportive management systems for project managers, informal multifunctional teams in concept development and market development, a stmctured needs identification process, and appointment of a process steward to monitor the innovation process, measure how it functions, and coordinate innovation projects. [Pg.133]

Most network polymers (the epoxies and the polyesters, for instance) are made by condensation reactions. The only difference is that one of the two reacting molecules is multifunctional (polyester is three-functional) so the reaction gives a three-dimensional lacework, not linear threads, and the resulting polymer is a thermoset. [Pg.255]

Carboxylic acids with multifunctional epoxides or epoxy functional monomers... [Pg.496]

In the case of Cleanser Chemicals, Inc., the company formed a multifunctional team to assess commonalities across its existing Safety, Loss Prevention, Security, Medical, Industrial Hygiene and Environment functions. As a result of this assessment, many common requirements and potential work processes were identified, including ... [Pg.57]

FIGURE 25.9 Fatty add synthase in animals contains all the functional groups and enzyme activities on a single multifunctional subunit. The active enzyme Is a head-to-tall dimer of Identical subunits. (Adapted from Wakit, S. J., Stoops,... [Pg.812]

Despite the introduction of new, improved methods of refining it has been necessary to enhance the performance of lubricants by the use of additives, either to reinforce existing qualities or to confer additional properties. Once additives were regarded with some suspicion —an oil that needed an additive was necessarily an inferior oil today they are an accepted feature of lubricants. Almost all quality lubricants on sale today contain one or more additives. An enormous range of additives are available for use in lubricants " , some produced by the oil companies and others provided by specialist manufacturers. Additives are usually named after their particular function, but many additives are multifunctional. Thus, an anti-wear additive may also protect a surface against corrosion. The main types of additives that can enhance the anti-corrosion behaviour of lubricants are listed in Table 2.22. [Pg.449]

The success of intramolecular conjugate additions of carbon-centered radicals in multifunctional contexts is noteworthy. Compound 57 (see Scheme 10), prepared by an interesting sequence starting from meto-toluic acid (54) (see 54 > 55 > 56 > 57), can be converted to the highly functionalized perhydroindane 58 through an intramolecular conjugate addition of a hindered secondary radical.21-22 This radical cyclization actually furnishes a 6 1 mixture of perhydroindane diastereoisomers, epimeric at C-7, in favor of 58 (96 % total yield). It should be noted that a substantially less strained cis-fused bicyclo[4.3.0] substructure is formed in this cyclization. [Pg.390]

During the course of an elegant synthesis of the multifunctional FR-900482 molecule [( )-43, Scheme 9], the Danishefsky group accomplished the assembly of tetracycle 42 using an intramolecular Heck arylation as a key step.24 In the crucial C-C bond forming reaction, exposure of aryl iodide 41 to a catalytic amount of tetra-kis(triphenylphosphine)palladium(o) and triethylamine in acetonitrile at 80 °C effects the desired Heck arylation, affording 42 in an excellent yield of 93 %. The impressive success of this cyclization reaction is noteworthy in view of the potentially sensitive functionality contained within 41. [Pg.574]

The architect continues to look for products that can he multifunctional. As an example in roofing, the product could perform a part or all of the functions. The roof has to provide structural integrity, temperature and sound insulation, vapor and moisture control, weather resistance, elastic qualities for change in weather, fire protection, aesthetic appeal, and so on. [Pg.246]

Like HATs, most functional HDACs are embedded in large multifunctional protein complexes, which also contain other chromatin modifying enzymes and coregulator proteins [1]. [Pg.594]

Interferons (EFNs) are a family of multifunctional secreted proteins in vertebrates. Their most prominent functions are their antiviral properties on homologous cells against a wide range of viruses. It is important to note that prior exposure to EFN is required to render cells resistant to viral infection and replication. In contrast to antibodies, EFNs have no direct neutralizing effect on viruses. [Pg.639]

Multifunctional initiators contain two or more radical generating functions within the one molecule. They can be considered in two distinct classes according... [Pg.96]

Multifunctional initiators contain two or more radical generating functions within the one molecule. The chemistry of these initiators has been the subject of several reviews.252 25 As long as the radical generating functions are sufficiently remote their decompositions are independent events. If decomposition occurs... [Pg.385]

The multifunctional initiators may be di- and tri-, azo- or peroxy-compounds of defined structure (c.g. 20256) or they may be polymeric azo- or peroxy-compounds where the radical generating functions may be present as side chains 57 or as part of the polymer backbone."58"261 Thus, amphiphilic block copolymers were synthesized using the polymeric initiator 21 formed from the reaction between an a,to-diol and AIBN (Scheme 7.22).26 Some further examples of multifunctional initiators were mentioned in Section 3.3.3.2. It is also possible to produce less well-defined multifunctional initiators containing peroxide functionality from a polymer substrate by autoxidalion or by ozonolysis.-0... [Pg.386]

The success of the multifunctional initiators in the preparation of block and graft copolymers depends critically on the kinetics and mechanism of radical production. In particular, the initiator efficiency, the susceptibility to and mechanism of transfer to initiator, and the relative stability of the various radical generating functions. Each of these factors has a substantial influence on the nature and homogeneity of the polymer formed. Features of the kinetics of polymerizations initiated by multifunctional initiators have been modeled by O Driscoll and Bevington 64 and Choi and Lei.265... [Pg.386]

A final class of multifunctional initiators is based on the use a (muUi)functional polymer and a low molecular weight redox agent. Radicals on the polymer chain arc generated from the polymer bound functionality by a redox reaction. Ideally, no free initiating species are formed. The best known of this class are the polyol-redox and related systems. Polymers containing hydroxy or glycol and related functionality are subject to one electron oxidation by species such as ceric ions or periodate (Scheme 7.23).266,267 Substrates such as cellulose,... [Pg.386]


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See also in sourсe #XX -- [ Pg.72 ]




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Functional groups multifunctional)

Multifunctional

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