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Substrate types

Another way to determine durabHity is to find successfuHy sealed, existing field instaHations. Sealant manufacturers often have case histories of successful instaHations. Adhesion performance can vary widely with sealant type, substrate type, and cleaning method. Eor this reason, it is important to understand the sealant s sensitivity to cleaning practices. Often with difficult-to-adhere substrates, a primer is used. Sealant manufacturers can provide recommendations as to which substrates require primers, what type of primers should be used, and how they should be appHed. [Pg.309]

PPO from tea reacts effectively with both 3 -4 and 3 -4 -5-hydroxylated catechins, with specificity for the o-diphenol (43,44). Studies defining the kinetics of PPO from tea in relation to substrate type are lacking as of this writing (ca 1997). Tea PPO has good functionaUty in the pH range 4.6—5.6 (43,45-48). [Pg.368]

The study of enzymes is important because every syndietic and degradation reaction in all living cells is controlled and catalyzed by specific enzymes. Many of these reactions are the soluble enzyme-soluble substrate type and are homogeneous in the liquid phase. [Pg.21]

Substrate type w w Role of H]0 in rate-determining step... [Pg.456]

Substrate Type of linkage involving Rha pnp- rhamnohydrolase (U/mg) RG- rhamnohydrolase (U/mg)... [Pg.238]

Portable Equipment. Chemical shoreline cleaning agents enhance removal of stranded oil from shoreline surfaces, but site-specific variables, physical and chemical properties of oil, and variations in substrate types influence the performance of shoreline cleaning agents. It is difficult to predict the performance for site-specific variables. Therefore on-site testing of shoreline cleaning agents with oil and local substrates is needed. [Pg.302]

Fig. 20.4. H-bond acceptor patterns observed two electron donor groups with a spatial in P-gp substrates. Type I units patterns separation of 4.6 + 0.6 A. A denotes a informed by electron donor pairs with a spatial bonding acceptor group (electron donor... Fig. 20.4. H-bond acceptor patterns observed two electron donor groups with a spatial in P-gp substrates. Type I units patterns separation of 4.6 + 0.6 A. A denotes a informed by electron donor pairs with a spatial bonding acceptor group (electron donor...
Separation technologies for different substrate types are compared in Table 2.1... [Pg.20]

Wada, T. Nishitani, M. Negami, T. Kohara, N. Ikeda, M. Terauchi, M. 1994. Microstructural characterization of substrate-type and superstrate-type CuInSe2 thin film solar cells. Proc. 12th European Photovoltaic Solar Energy Conf. pp. 1542-1545. [Pg.230]

There are many ways to categorize the oxidation of double bonds as they undergo a myriad of oxidative transformations leading to many product types including epoxides, ketones, diols, endoperoxides, ozonides, allylic alcohols and many others. Rather than review the oxidation of dienes by substrate type or product obtained, we have chosen to classify the oxidation reactions of dienes and polyenes by the oxidation reagent or system used, since each have a common reactivity profile. Thus, similar reactions with each specific oxidant can be carried out on a variety of substrates and can be easily compared. [Pg.891]

When 1,3-dienes containing a tethered alcohol are subjected to Wacker-type reactions, the initial intramolecular oxypalladation event creates a 7r-allylpalladium species, which can then undergo an additional bond-forming process to effect an overall 1,4-difunctionalization of the diene with either cis- or // -stereochemistry (Scheme 18).399 An array of substrate types has been shown to participate in this reaction to generate both five- and six-membered fused or ro-oxacycles.435-437 Employing chiral benzoquinone ligands, progress toward the development of an asymmetric variant of this reaction has also been recorded, albeit with only modest levels of enantioselectivity (up to 55% ee).438... [Pg.682]

Chiral amines were always considered important targets for synthetic chemists, and attempts to prepare such compounds enantioselectively date back to quite early times. Selected milestones for the development of enantioselective catalysts for the reduction of C = N functions are listed in Table 34.1. At first, only heterogeneous hydrogenation catalysts such as Pt black, Pd/C or Raney nickel were applied. These were modified with chiral auxiliaries in the hope that some induction - that is, transfer of chirality from the auxiliary to the reactant -might occur. These efforts were undertaken on a purely empirical basis, without any understanding of what might influence the desired selectivity. Only very few substrate types were studied and, not surprisingly, enantioselectivities were... [Pg.1193]

Is homogeneous asymmetric hydrogenation a mature manufacturing technology The answer is clearly NOT YET - with, perhaps, the exception of a few privileged substrate types. Our definition of a mature manufacturing technology can be summarized as follows ... [Pg.1317]

Similar schemes can be developed easily for analogous reactions of acceptor-substituted polyenes. For example, a triene with an acceptor group in 1-position can form six regioi-someric products of Michael addition and electrophilic capture, and each of these exists as E/Z stereoisomers, diastereomers and/or enantiomers. Thus, reactions of this type are only useful if both the regio- and stereoselectivity can be controlled fortunately, only one isomeric Michael adduct is formed in many cases. This is true in particular for polyunsaturated Michael acceptors which bear at least one triple bond besides one or more double bonds. An additional feature of the latter substrate type is that nucleophilic additions can... [Pg.646]

For convenience, the reactions are reviewed according to substrate type. [Pg.317]

T. Nakanishi, "Substrate Type, Planar Solid Oxide Fuel Cell," Fuji Electric, Fuel Cell Seminar Program and Abstracts, 1992 Fuel Cell Seminar, Tucson, AZ, November 29 -December 2, 1992. [Pg.196]

Fig. 10 Diphosphine ligand 9. Comparison of the best results obtained in the b-catalyzed hydrogenation of several substrate types using hgands 5 and 9... Fig. 10 Diphosphine ligand 9. Comparison of the best results obtained in the b-catalyzed hydrogenation of several substrate types using hgands 5 and 9...
There is a need for an accurate assessment of the mechanism of cathodic debonding of thick adherends. This would contribute to better control over the selection of formulations resistant to attack. One of the objectives of this work was to develop an accelerated screening test. The screening test was used to evaluate the relative performance profiles of a number of commercial adhesives which were recommended for marine applications. It is hoped that a screening test such as this one could be used to isolate measurable primer properties which can be related to the long term prospectus of the primer, and the variability of this prospectus under permutation of substrate type or additives. [Pg.170]

Initial bond strength depended heavily upon substrate type rather than surface preparation. Regardless of pretreatment, initial bond strength was highest when using Al-Tl adherends and lowest when the adherends were galvanized steel. [Pg.193]

The three hydrolytic enzymes that have been discussed, a-chymo-trypsin, carboxypeptidase A, and lysozyme, cover a wide range of substrate types and mechanistic possibilities. Formulation of principles which might apply to enzymatic catalysis in general is difficult from such a small sampling, but certain features of the enzymatic and model reactions warrant some comment. [Pg.115]

The geochemical signature of the XY orebody within these soils is likely derived from detrital sources, not hydrochemical sources. A hydrochemical signature of the XY orebody was not isolated in these soils by this protocol. Perhaps a less aggressive partial leach protocol may be more suitable given the substrate type. [Pg.42]


See other pages where Substrate types is mentioned: [Pg.186]    [Pg.532]    [Pg.421]    [Pg.640]    [Pg.113]    [Pg.674]    [Pg.302]    [Pg.390]    [Pg.121]    [Pg.24]    [Pg.26]    [Pg.27]    [Pg.902]    [Pg.337]    [Pg.184]    [Pg.1210]    [Pg.203]    [Pg.84]    [Pg.86]    [Pg.86]    [Pg.435]    [Pg.41]    [Pg.310]    [Pg.56]    [Pg.203]    [Pg.150]    [Pg.406]    [Pg.6]    [Pg.180]    [Pg.183]   
See also in sourсe #XX -- [ Pg.128 ]




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